# RGD-PIPELINE: ftp-file-extracts
# MODULE: annotations-version-1.2.0 (Jul 27, 2026)
# GENERATED-ON: 2026/08/15
# 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 '|'
#
# MIGRATION NOTE (July 2026): these files were previously located in the
#   'annotated_rgd_objects_by_ontology/with_terms' directory and named using the organism
#   genus (f.e. 'rattus_terms_go'). They are now located in the 'annotations/with_terms' directory,
#   named with the RGD species short name (f.e. 'rat_terms_go.txt.gz'), and gzip-compressed.
#
#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
10035815	Gm38999	predicted gene, 38999	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0008878	abnormal DNA methylation during gametogenesis		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
10035815	Gm38999	predicted gene, 38999	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20250612	MGI			PMID:38359823
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: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: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:0014956	decreased mitochondria enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:11590124
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: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: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: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: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:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:12893739
10058	Acadvl	acyl-Coenzyme A dehydrogenase, very long chain	gene	MP:0014904	abnormal fat cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:16199475
10058	Acadvl	acyl-Coenzyme A dehydrogenase, very long chain	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:11590124
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
10058	Acadvl	acyl-Coenzyme A dehydrogenase, very long chain	gene	MP:0031710	polymorphic ventricular tachycardia		IAGP		N	RGD:5509061	20260514	MGI			PMID:12893739
10060	Acat1	acetyl-Coenzyme A acetyltransferase 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20240523	MGI			
10060	Acat1	acetyl-Coenzyme A acetyltransferase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	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 morphology		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: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:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:26398936
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			
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: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:0014602	decreased female mating frequency		IAGP		N	RGD:5509061	20250206	MGI			PMID:12409213
10084	Adcyap1	adenylate cyclase activating polypeptide 1	gene	MP:0020220	decreased tear production		IAGP		N	RGD:5509061	20170615	MGI			PMID:27345595
10084	Adcyap1	adenylate cyclase activating polypeptide 1	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:23500093
10084	Adcyap1	adenylate cyclase activating polypeptide 1	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:15217792
10084	Adcyap1	adenylate cyclase activating polypeptide 1	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:15217792
10084	Adcyap1	adenylate cyclase activating polypeptide 1	gene	MP:0030762	decreased adrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:11756684
10084	Adcyap1	adenylate cyclase activating polypeptide 1	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:11579206
10084	Adcyap1	adenylate cyclase activating polypeptide 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:15217792
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792006
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483244
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466423
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466423
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11193864
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792006
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032869
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466423
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792830
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:11466423
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792006
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792006
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11193864
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11193864
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792006
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466423
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210422	MGI			
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:11425915
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0020475	delayed circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:11425915
10085	Adcyap1r1	adenylate cyclase activating polypeptide 1 receptor 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:11483244
10086	Add1	adducin 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0001893	non-obstructive hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0008850	increased hemoglobin concentration distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0008935	decreased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10086	Add1	adducin 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723693
10087	Add2	adducin 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10087	Add2	adducin 2	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10988280
10087	Add2	adducin 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728854
10087	Add2	adducin 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728854
10087	Add2	adducin 2	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728854
10087	Add2	adducin 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728854
10087	Add2	adducin 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10087	Add2	adducin 2	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728854
10087	Add2	adducin 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728854
10087	Add2	adducin 2	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10087	Add2	adducin 2	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10087	Add2	adducin 2	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10087	Add2	adducin 2	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10087	Add2	adducin 2	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10087	Add2	adducin 2	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728854
10087	Add2	adducin 2	gene	MP:0002923	increased post-tetanic potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728854
10087	Add2	adducin 2	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10988280
10087	Add2	adducin 2	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10988280
10087	Add2	adducin 2	gene	MP:0006265	increased pulse pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10988280
10087	Add2	adducin 2	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485892
10087	Add2	adducin 2	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:10845937
10087	Add2	adducin 2	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:19425068
10088	Add3	adducin 3	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10088	Add3	adducin 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10088	Add3	adducin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10088	Add3	adducin 3	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10088	Add3	adducin 3	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10088	Add3	adducin 3	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10088	Add3	adducin 3	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10088	Add3	adducin 3	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19425068
10088	Add3	adducin 3	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:19425068
10090	Adh1	alcohol dehydrogenase 1 (class I)	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11836246
10090	Adh1	alcohol dehydrogenase 1 (class I)	gene	MP:0005443	abnormal ethanol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10358022
10090	Adh1	alcohol dehydrogenase 1 (class I)	gene	MP:0005443	abnormal ethanol metabolism		IAGP		N	RGD:5509061	20231019	MGI			PMID:36224745
10090	Adh1	alcohol dehydrogenase 1 (class I)	gene	MP:0005444	abnormal retinol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10358022
10090	Adh1	alcohol dehydrogenase 1 (class I)	gene	MP:0005444	abnormal retinol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11836246
10090	Adh1	alcohol dehydrogenase 1 (class I)	gene	MP:0005444	abnormal retinol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12027900
10090	Adh1	alcohol dehydrogenase 1 (class I)	gene	MP:0005444	abnormal retinol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12851412
10090	Adh1	alcohol dehydrogenase 1 (class I)	gene	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20231019	MGI			PMID:10358022
10090	Adh1	alcohol dehydrogenase 1 (class I)	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11836246
10091	Adk	adenosine kinase	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
10091	Adk	adenosine kinase	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210826	MGI			
10091	Adk	adenosine kinase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210826	MGI			
10091	Adk	adenosine kinase	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20210826	MGI			
10091	Adk	adenosine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
10091	Adk	adenosine kinase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
10091	Adk	adenosine kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
10091	Adk	adenosine kinase	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20210826	MGI			
10091	Adk	adenosine kinase	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0004882	enlarged lung		IEA		N	RGD:5509061	20210826	MGI			
10091	Adk	adenosine kinase	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20211021	MGI			
10091	Adk	adenosine kinase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
10091	Adk	adenosine kinase	gene	MP:0012348	decreased susceptibility to induction of seizure by inducing agent		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10091	Adk	adenosine kinase	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:11997462
10091	Adk	adenosine kinase	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:11997462
10092	Adora2a	adenosine A2a receptor	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230601	MGI			
10092	Adora2a	adenosine A2a receptor	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20938208
10092	Adora2a	adenosine A2a receptor	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20938208
10092	Adora2a	adenosine A2a receptor	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531422
10092	Adora2a	adenosine A2a receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10771351
10092	Adora2a	adenosine A2a receptor	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129427
10092	Adora2a	adenosine A2a receptor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0002698	abnormal sclera morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484596
10092	Adora2a	adenosine A2a receptor	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
10092	Adora2a	adenosine A2a receptor	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20210826	MGI			
10092	Adora2a	adenosine A2a receptor	gene	MP:0002975	vascular smooth muscle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20938208
10092	Adora2a	adenosine A2a receptor	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0003100	myopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484596
10092	Adora2a	adenosine A2a receptor	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15602504
10092	Adora2a	adenosine A2a receptor	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16280580
10092	Adora2a	adenosine A2a receptor	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:20938208
10092	Adora2a	adenosine A2a receptor	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
10092	Adora2a	adenosine A2a receptor	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20938208
10092	Adora2a	adenosine A2a receptor	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10092	Adora2a	adenosine A2a receptor	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210826	MGI			
10092	Adora2a	adenosine A2a receptor	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
10092	Adora2a	adenosine A2a receptor	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531422
10092	Adora2a	adenosine A2a receptor	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531422
10092	Adora2a	adenosine A2a receptor	gene	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525287
10092	Adora2a	adenosine A2a receptor	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12700712
10092	Adora2a	adenosine A2a receptor	gene	MP:0009586	increased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262401
10092	Adora2a	adenosine A2a receptor	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10771351
10092	Adora2a	adenosine A2a receptor	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12700712
10092	Adora2a	adenosine A2a receptor	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15602504
10092	Adora2a	adenosine A2a receptor	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965471
10092	Adora2a	adenosine A2a receptor	gene	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20141003	MGI			PMID:11166335
10092	Adora2a	adenosine A2a receptor	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
10092	Adora2a	adenosine A2a receptor	gene	MP:0010758	increased right ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20938208
10092	Adora2a	adenosine A2a receptor	gene	MP:0012348	decreased susceptibility to induction of seizure by inducing agent		IAGP		N	RGD:5509061	20170119	MGI			PMID:27903722
10092	Adora2a	adenosine A2a receptor	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
10093	Adora3	adenosine A3 receptor	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12817015
10093	Adora3	adenosine A3 receptor	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660615
10093	Adora3	adenosine A3 receptor	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20150101	MGI			PMID:16157310
10093	Adora3	adenosine A3 receptor	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12220556
10093	Adora3	adenosine A3 receptor	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10699369
10093	Adora3	adenosine A3 receptor	gene	MP:0003022	increased coronary flow rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12003827
10093	Adora3	adenosine A3 receptor	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273734
10093	Adora3	adenosine A3 receptor	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:10699369
10093	Adora3	adenosine A3 receptor	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12003827
10093	Adora3	adenosine A3 receptor	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12817015
10093	Adora3	adenosine A3 receptor	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388399
10093	Adora3	adenosine A3 receptor	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12220556
10093	Adora3	adenosine A3 receptor	gene	MP:0005260	ocular hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12202525
10093	Adora3	adenosine A3 receptor	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388399
10093	Adora3	adenosine A3 receptor	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660615
10093	Adora3	adenosine A3 receptor	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12817015
10093	Adora3	adenosine A3 receptor	gene	MP:0008763	abnormal mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12817015
10093	Adora3	adenosine A3 receptor	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20150101	MGI			PMID:16157310
10094	Adprh	ADP-ribosylarginine hydrolase	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526733
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326654
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11222061
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11115730
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11222061
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11222061
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466664
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519431
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466664
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:11222061
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0003823	increased left ventricle developed pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519431
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466664
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11115730
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0004184	abnormal baroreceptor physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466664
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519431
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466664
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326654
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466664
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005406	abnormal heart size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466664
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923452
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923452
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20160310	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20160310	MGI			PMID:14581480
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782680
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:17951539
10096	Adra1b	adrenergic receptor, alpha 1b	gene	MP:0031635	increased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:12782680
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992256
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385696
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8670421
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20170105	MGI			
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10647009
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992256
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20190110	MGI			
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276088
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385696
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20160211	MGI			
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0005447	abnormal synaptic norepinephrine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:10647009
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20190110	MGI			
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:19225179
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10098	Adra2a	adrenergic receptor, alpha 2a	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20160211	MGI			
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8670422
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8670422
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10647009
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8670422
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10101	Adra2b	adrenergic receptor, alpha 2b	gene	MP:0011147	increased mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729197
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:9526020
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10647009
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20151119	MGI			PMID:10523817
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0005447	abnormal synaptic norepinephrine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:10647009
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:10051760
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:11642653
10103	Adra2c	adrenergic receptor, alpha 2c	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068299
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10358009
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8693001
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:10358009
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10358009
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10358009
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10358009
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:10358009
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:8693001
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0009119	increased brown fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10106	Adrb1	adrenergic receptor, beta 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8693001
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9276726
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:9276726
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9276726
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493988
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0009119	increased brown fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0009300	increased parametrial fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493988
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493988
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9276726
10110	Adrb3	adrenergic receptor, beta 3	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161655
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: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: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: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:0014600	increased susceptibility to hyperoxia-induced injury		IAGP		N	RGD:5509061	20250206	MGI			PMID:15123765
10127	Ahr	aryl-hydrocarbon receptor	gene	MP:0014645	decreased optokinetic reflex		IAGP		N	RGD:5509061	20250306	MGI			PMID:23301081
10127	Ahr	aryl-hydrocarbon receptor	gene	MP:0014684	impaired spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:24174576
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: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
10129	Ak1	adenylate kinase 1	gene	MP:0014998	abnormal glucose metabolism		IAGP		N	RGD:5509061	20260611	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	Akt serine/threonine kinase 2	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:20837017
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22275470
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001238	thin epidermis stratum spinosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883618
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11387480
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348245
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442925
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442925
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210696
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22275470
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11387480
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883618
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883618
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442925
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002310	decreased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20150709	MGI			PMID:20837017
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22275470
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22275470
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883618
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442925
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442925
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883618
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11387480
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348245
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11387480
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883618
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883618
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883618
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442925
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0009167	increased pancreatic islet number		IAGP		N	RGD:5509061	20170803	MGI			PMID:11387480
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289493
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883618
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348245
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0009371	increased theca cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22275470
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782654
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20150709	MGI			PMID:20837017
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16923958
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:12843127
10132	Akt2	Akt serine/threonine kinase 2	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:11387480
10132	Akt2	Akt serine/threonine kinase 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: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:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20250206	MGI			PMID:22527485
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: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:0014782	increased liver enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:25453901
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:0003917	increased kidney weight		IEA		N	RGD:5509061	20260402	MGI			
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:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
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:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20251030	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:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
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:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
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:0001293	anophthalmia		IEA		N	RGD:5509061	20260402	MGI			
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:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
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	20170413	MGI			PMID:19893577
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	20211125	MGI			PMID:30374053
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20250925	MGI			PMID:9037065
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:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:15716339
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0003449	abnormal intestine 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:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
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:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20260402	MGI			
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: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:0014754	abnormal tumor progression		IAGP		N	RGD:5509061	20250925	MGI			PMID:26527802
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014755	increased tumor cell proliferation		IAGP		N	RGD:5509061	20250925	MGI			PMID:20852630
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:23741059
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:29844172
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:30374053
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250925	MGI			PMID:31662330
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250925	MGI			PMID:33879799
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:21467224
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:23741059
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:29844172
10166	Apc	APC, WNT signaling pathway regulator	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:12130785
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: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
10180	Apod	apolipoprotein D	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	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: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:0004080	abnormal nucleus accumbens morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:16797122
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: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
10183	Aqp4	aquaporin 4	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250911	MGI			PMID:11406631
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: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: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: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:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:12370412
10187	Ar	androgen receptor	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:14745012
10187	Ar	androgen receptor	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:14745012
10187	Ar	androgen receptor	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:17406000
10187	Ar	androgen receptor	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:17406000
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:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
10191	Arrb1	arrestin, beta 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10191	Arrb1	arrestin, beta 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10191	Arrb1	arrestin, beta 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10191	Arrb1	arrestin, beta 1	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10191	Arrb1	arrestin, beta 1	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10191	Arrb1	arrestin, beta 1	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10191	Arrb1	arrestin, beta 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10191	Arrb1	arrestin, beta 1	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10191	Arrb1	arrestin, beta 1	gene	MP:0011148	decreased mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10191	Arrb1	arrestin, beta 1	gene	MP:0031635	increased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:9400383
10192	Arrb2	arrestin, beta 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20220519	MGI			
10192	Arrb2	arrestin, beta 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
10192	Arrb2	arrestin, beta 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210520	MGI			
10192	Arrb2	arrestin, beta 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10617462
10192	Arrb2	arrestin, beta 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:10617462
10192	Arrb2	arrestin, beta 2	gene	MP:0002274	abnormal type I pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
10192	Arrb2	arrestin, beta 2	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032308
10192	Arrb2	arrestin, beta 2	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16378096
10192	Arrb2	arrestin, beta 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
10192	Arrb2	arrestin, beta 2	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0008552	abnormal circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16378096
10192	Arrb2	arrestin, beta 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16378096
10192	Arrb2	arrestin, beta 2	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16378096
10192	Arrb2	arrestin, beta 2	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16378096
10192	Arrb2	arrestin, beta 2	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16378096
10192	Arrb2	arrestin, beta 2	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16378096
10192	Arrb2	arrestin, beta 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060823
10192	Arrb2	arrestin, beta 2	gene	MP: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 layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:7773285
10194	Ascl2	achaete-scute family bHLH transcription factor 2	gene	MP:0012100	absent spongiotrophoblast layer		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 induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716718
10199	Atm	ataxia telangiectasia mutated	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8689683
10199	Atm	ataxia telangiectasia mutated	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		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 induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389091
10199	Atm	ataxia telangiectasia mutated	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429352
10199	Atm	ataxia telangiectasia mutated	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
10199	Atm	ataxia telangiectasia mutated	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
10199	Atm	ataxia telangiectasia mutated	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		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: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:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11389091
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: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:0014961	increased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22025725
10207	Atp1a3	ATPase, Na+/K+ transporting, alpha 3 polypeptide	gene	MP:0020424	increased kindling response		IAGP		N	RGD:5509061	20180712	MGI			PMID:25523819
10207	Atp1a3	ATPase, Na+/K+ transporting, alpha 3 polypeptide	gene	MP:0020424	increased kindling response		IAGP		N	RGD:5509061	20180920	MGI			PMID:30071271
10207	Atp1a3	ATPase, Na+/K+ transporting, alpha 3 polypeptide	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:22025725
10207	Atp1a3	ATPase, Na+/K+ transporting, alpha 3 polypeptide	gene	MP:0031201	hemiparesis		IAGP		N	RGD:5509061	20210218	MGI			PMID:25523819
10207	Atp1a3	ATPase, Na+/K+ transporting, alpha 3 polypeptide	gene	MP:0031202	hemiplegia		IAGP		N	RGD:5509061	20210218	MGI			PMID:25523819
10207	Atp1a3	ATPase, Na+/K+ transporting, alpha 3 polypeptide	gene	MP:0031202	hemiplegia		IAGP		N	RGD:5509061	20210218	MGI			PMID:30071271
10207	Atp1a3	ATPase, Na+/K+ transporting, alpha 3 polypeptide	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22025725
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0000756	forelimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9801359
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9801359
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8793730
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9801359
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9801359
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9801359
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9801359
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9801359
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7525597
10208	Atp1b2	ATPase, Na+/K+ transporting, beta 2 polypeptide	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:9801359
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20200402	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20200402	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20200402	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20200402	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20200402	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20250508	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20200402	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
10209	Atp1b3	ATPase, Na+/K+ transporting, beta 3 polypeptide	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20250508	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: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
10211	Atp2b2	ATPase, Ca++ transporting, plasma membrane 2	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	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: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:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20260813	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: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	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: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:0014958	decreased lung enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:20889
10215	Atp7a	ATPase, copper transporting, alpha polypeptide	gene	MP:0014961	increased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:9342151
10215	Atp7a	ATPase, copper transporting, alpha polypeptide	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:9342151
10215	Atp7a	ATPase, copper transporting, alpha polypeptide	gene	MP:0014970	decreased muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:9342151
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:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0001785	edema		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0003066	increased liver copper level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0003103	liver degeneration		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0003333	liver fibrosis		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0005376	homeostasis/metabolism phenotype		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0006350	increased circulating copper level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0014427	increased circulating hyaluronic acid level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0014501	increased circulating protein level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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:0014539	increased copper level		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0014549	increased zinc level		IAGP		N	RGD:5509061	20240912	MGI			PMID:8040371
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
10217	Atp7b	ATPase, copper transporting, beta polypeptide	gene	MP:0031022	hepatic megalocytosis		IAGP		N	RGD:5509061	20260305	MGI			PMID:39334421
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 morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804210
10226	Bax	BCL2-associated X protein	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804210
10226	Bax	BCL2-associated X protein	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804210
10226	Bax	BCL2-associated X protein	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804210
10226	Bax	BCL2-associated X protein	gene	MP:0000909	abnormal facial motor nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8816704
10226	Bax	BCL2-associated X protein	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16928866
10226	Bax	BCL2-associated X protein	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16928866
10226	Bax	BCL2-associated X protein	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16928866
10226	Bax	BCL2-associated X protein	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12741988
10226	Bax	BCL2-associated X protein	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15836427
10226	Bax	BCL2-associated X protein	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:21151121
10226	Bax	BCL2-associated X protein	gene	MP:0001011	abnormal superior cervical ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8816704
10226	Bax	BCL2-associated X protein	gene	MP:0001025	abnormal sympathetic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8816704
10226	Bax	BCL2-associated X protein	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
10226	Bax	BCL2-associated X protein	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
10226	Bax	BCL2-associated X protein	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
10226	Bax	BCL2-associated X protein	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20160804	MGI			PMID:24453327
10226	Bax	BCL2-associated X protein	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10894153
10226	Bax	BCL2-associated X protein	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988273
10226	Bax	BCL2-associated X protein	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:16270031
10226	Bax	BCL2-associated X protein	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7569956
10226	Bax	BCL2-associated X protein	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10894153
10226	Bax	BCL2-associated X protein	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16270031
10226	Bax	BCL2-associated X protein	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16414041
10226	Bax	BCL2-associated X protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
10226	Bax	BCL2-associated X protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16270031
10226	Bax	BCL2-associated X protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
10226	Bax	BCL2-associated X protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22884324
10226	Bax	BCL2-associated X protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160331	MGI			PMID:26203146
10226	Bax	BCL2-associated X protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804210
10226	Bax	BCL2-associated X protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117778
10226	Bax	BCL2-associated X protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22884324
10226	Bax	BCL2-associated X protein	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16928866
10226	Bax	BCL2-associated X protein	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
10226	Bax	BCL2-associated X protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10894153
10226	Bax	BCL2-associated X protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16270031
10226	Bax	BCL2-associated X protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7569956
10226	Bax	BCL2-associated X protein	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281459
10226	Bax	BCL2-associated X protein	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24036309
10226	Bax	BCL2-associated X protein	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16928866
10226	Bax	BCL2-associated X protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288109
10226	Bax	BCL2-associated X protein	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
10226	Bax	BCL2-associated X protein	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16928866
10226	Bax	BCL2-associated X protein	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
10226	Bax	BCL2-associated X protein	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16270031
10226	Bax	BCL2-associated X protein	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7569956
10226	Bax	BCL2-associated X protein	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19755105
10226	Bax	BCL2-associated X protein	gene	MP:0002982	abnormal primordial germ cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17107997
10226	Bax	BCL2-associated X protein	gene	MP:0002982	abnormal primordial germ cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
10226	Bax	BCL2-associated X protein	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
10226	Bax	BCL2-associated X protein	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10744634
10226	Bax	BCL2-associated X protein	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11150333
10226	Bax	BCL2-associated X protein	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8816704
10226	Bax	BCL2-associated X protein	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9096145
10226	Bax	BCL2-associated X protein	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:22884324
10226	Bax	BCL2-associated X protein	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15836427
10226	Bax	BCL2-associated X protein	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12741988
10226	Bax	BCL2-associated X protein	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247919
10226	Bax	BCL2-associated X protein	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
10226	Bax	BCL2-associated X protein	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
10226	Bax	BCL2-associated X protein	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16270031
10226	Bax	BCL2-associated X protein	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10894153
10226	Bax	BCL2-associated X protein	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23805138
10226	Bax	BCL2-associated X protein	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7569956
10226	Bax	BCL2-associated X protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10894153
10226	Bax	BCL2-associated X protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16270031
10226	Bax	BCL2-associated X protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281459
10226	Bax	BCL2-associated X protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7569956
10226	Bax	BCL2-associated X protein	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8816704
10226	Bax	BCL2-associated X protein	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0006006	increased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15836427
10226	Bax	BCL2-associated X protein	gene	MP:0006006	increased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
10226	Bax	BCL2-associated X protein	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16928866
10226	Bax	BCL2-associated X protein	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11150333
10226	Bax	BCL2-associated X protein	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0008206	increased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
10226	Bax	BCL2-associated X protein	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16270031
10226	Bax	BCL2-associated X protein	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281459
10226	Bax	BCL2-associated X protein	gene	MP:0008390	abnormal primordial germ cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17107997
10226	Bax	BCL2-associated X protein	gene	MP:0008391	abnormal primordial germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
10226	Bax	BCL2-associated X protein	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
10226	Bax	BCL2-associated X protein	gene	MP:0008468	absent muscle spindles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12741988
10226	Bax	BCL2-associated X protein	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0008485	increased muscle spindle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247919
10226	Bax	BCL2-associated X protein	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804210
10226	Bax	BCL2-associated X protein	gene	MP:0008870	increased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988273
10226	Bax	BCL2-associated X protein	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804210
10226	Bax	BCL2-associated X protein	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0009083	uterus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988273
10226	Bax	BCL2-associated X protein	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676052
10226	Bax	BCL2-associated X protein	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:19706873
10226	Bax	BCL2-associated X protein	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804210
10226	Bax	BCL2-associated X protein	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22884324
10226	Bax	BCL2-associated X protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
10226	Bax	BCL2-associated X protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22884324
10226	Bax	BCL2-associated X protein	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9096145
10226	Bax	BCL2-associated X protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160331	MGI			PMID:26203146
10226	Bax	BCL2-associated X protein	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16270031
10226	Bax	BCL2-associated X protein	gene	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm		IAGP		N	RGD:5509061	20160804	MGI			PMID:24453327
10226	Bax	BCL2-associated X protein	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20180705	MGI			PMID:27452460
10226	Bax	BCL2-associated X protein	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:15578095
10226	Bax	BCL2-associated X protein	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:7569956
10226	Bax	BCL2-associated X protein	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:7569956
10227	Bcan	brevican	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370289
10227	Bcan	brevican	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370289
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20181227	MGI			
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20240307	MGI			PMID:33944778
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200402	MGI			
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10228	Bckdha	branched chain ketoacid dehydrogenase E1, alpha polypeptide	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20191017	MGI			PMID:31435015
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000372	irregular coat pigmentation		IEA		N	RGD:5509061	20111116	MGI			
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000909	abnormal facial motor nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001011	abnormal superior cervical ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001025	abnormal sympathetic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749373
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321489
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414660
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414660
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749373
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20181206	MGI			PMID:28806762
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982684
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15708569
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002955	increased compensatory renal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950951
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749373
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950951
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15708569
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749373
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628407
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20150702	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982684
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982684
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:18988889
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005457	abnormal percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0006057	decreased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15708569
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0006405	abnormal L3 dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321489
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20150702	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982684
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982684
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982684
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982684
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749373
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8755480
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982684
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008961	abnormal basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0008962	abnormal carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009051	dilated distal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009051	dilated distal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606958
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009322	increased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009341	decreased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009361	abnormal primordial ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628407
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:11146504
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009641	kidney degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15708569
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:20144786
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0010979	small ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0010982	abnormal ureteric bud elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0010985	abnormal kidney mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651893
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011080	increased macrophage apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18988889
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011365	small metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011365	small metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011369	increased renal glomerulus apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011376	abnormal kidney corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011408	renal tubule hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8623928
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011408	renal tubule hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011425	abnormal kidney interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011430	mesangiolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8760259
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011457	abnormal metanephric ureteric bud development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7840250
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011483	renal glomerular synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011498	abnormal glomerular capsule parietal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011500	decreased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011502	parietal capsular epithelium metaplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0011871	podocyte hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794553
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20160310	MGI			PMID:7812968
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0020084	short ears		IAGP		N	RGD:5509061	20170914	MGI			PMID:11709185
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0030188	round snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:8402909
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0030188	round snout		IAGP		N	RGD:5509061	20171109	MGI			PMID:8170972
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0030967	abnormal circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:22258505
10230	Bcl2	B cell leukemia/lymphoma 2	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:22258505
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452647
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560214
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956243
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7775424
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002829	abnormal juxtaglomerular apparatus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452647
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497152
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452647
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452647
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452647
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497152
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497152
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452647
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0010145	abnormal spermatic cord morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0011300	abnormal juxtaglomerular cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560214
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0011347	abnormal kidney medullary ray morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015607
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0011638	abnormal mitochondrial chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10232	Bdkrb2	bradykinin receptor, beta 2	gene	MP:0011742	decreased urine nitrite level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560214
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9973328
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:10363708
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514401
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514401
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130183
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15115821
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15115821
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023662
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446138
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987955
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000907	small mesencephalic trigeminal nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000907	small mesencephalic trigeminal nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000959	abnormal somatic sensory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000960	abnormal sensory ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568031
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568031
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364058
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126035
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009525
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001007	abnormal sympathetic system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9786221
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001021	small L4 dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001021	small L4 dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001021	small L4 dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364058
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001026	abnormal adrenergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9786221
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995552
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364058
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001085	small petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001085	small petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001085	small petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001085	small petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364058
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364058
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364058
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023662
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19158294
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130183
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20231123	MGI			PMID:32492978
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130183
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568031
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478623
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10363708
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130183
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611369
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023662
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:19158294
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023662
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130183
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249684
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478623
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987955
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001411	spinning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001411	spinning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001411	spinning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023662
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:16697351
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611369
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20231123	MGI			PMID:32492978
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249684
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249684
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023662
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12971897
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249684
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204444
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568031
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001499	abnormal kindling response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15233915
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15115821
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987955
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446138
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130183
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568031
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568031
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8139657
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130183
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568031
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568031
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611369
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446138
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579207
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12971897
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136973
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446138
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130183
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9786221
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611369
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22492034
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20231123	MGI			PMID:32492978
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10334567
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364058
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611369
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620975
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137432
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364058
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478623
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130183
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9472042
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568031
10235	Bdnf	brain derived neurotrophic factor	gene	MP: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: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:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:22492034
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:0031333	decreased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:19293383
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:16697351
10235	Bdnf	brain derived neurotrophic factor	gene	MP:0031752	decreased inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20260813	MGI			PMID:19293383
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:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333348
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:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333348
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
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: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 induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10881179
10246	Brca1	breast cancer 1, early onset	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12555066
10246	Brca1	breast cancer 1, early onset	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19996295
10246	Brca1	breast cancer 1, early onset	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		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: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: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: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:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:12642502
10246	Brca1	breast cancer 1, early onset	gene	MP:0014699	increased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:18343216
10246	Brca1	breast cancer 1, early onset	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:23509290
10246	Brca1	breast cancer 1, early onset	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:25066119
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 induced cell death		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: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:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	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:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20251023	MGI			PMID:35690792
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: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
10251	Bsn	bassoon	gene	MP:0014711	decreased synaptic vesicle readily releasable pool size		IAGP		N	RGD:5509061	20250814	MGI			PMID:15829963
10254	Tspo	translocator protein	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
10254	Tspo	translocator protein	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	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
10255	C2	complement C2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0000315	hemoglobinuria		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0001860	liver inflammation		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0002083	premature death		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
10256	C3	complement component 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0003606	kidney failure		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20251030	MGI			PMID:10811844
10256	C3	complement component 3	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0005161	hematuria		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11801636
10256	C3	complement component 3	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
10256	C3	complement component 3	gene	MP:0005327	abnormal mesangial cell morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0005505	thrombocytosis		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
10256	C3	complement component 3	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
10256	C3	complement component 3	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
10256	C3	complement component 3	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
10256	C3	complement component 3	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
10256	C3	complement component 3	gene	MP:0011454	abnormal glomerular endothelium fenestra morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
10256	C3	complement component 3	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0011566	abnormal complement protein level		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0012610	increased complement C5 level		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
10256	C3	complement component 3	gene	MP:0014783	decreased liver enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:19620784
10256	C3	complement component 3	gene	MP:0020153	abnormal urine albumin level		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20250807	MGI			PMID:33288630
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: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: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: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: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:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:25855180
10265	Cacna1a	calcium channel, voltage-dependent, P/Q type, alpha 1A subunit	gene	MP:0014814	increased brain glucose metabolism		IAGP		N	RGD:5509061	20251204	MGI			PMID:1486501
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: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
10265	Cacna1a	calcium channel, voltage-dependent, P/Q type, alpha 1A subunit	gene	MP:0031332	abnormal inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:21411672
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: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:0015056	increased synaptic vesicle number		IAGP		N	RGD:5509061	20260813	MGI			PMID:17660813
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: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: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 induced cell death		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:0012447	thick cerebellar granule layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:8934524
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	RGD:5509061	20141030	MGI			PMID:25016930
10297	Cbs	cystathionine beta-synthase	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16984962
10297	Cbs	cystathionine beta-synthase	gene	MP:0008876	decreased uterine NK cell number		IAGP		N	RGD:5509061	20240502	MGI			PMID:22617046
10297	Cbs	cystathionine beta-synthase	gene	MP:0008957	abnormal placenta junctional zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16984962
10297	Cbs	cystathionine beta-synthase	gene	MP:0009007	short estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16984962
10297	Cbs	cystathionine beta-synthase	gene	MP:0009012	short diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16984962
10297	Cbs	cystathionine beta-synthase	gene	MP:0009018	short estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16984962
10297	Cbs	cystathionine beta-synthase	gene	MP:0009020	prolonged metestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16984962
10297	Cbs	cystathionine beta-synthase	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20141030	MGI			PMID:25016930
10297	Cbs	cystathionine beta-synthase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20638879
10297	Cbs	cystathionine beta-synthase	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16984962
10297	Cbs	cystathionine beta-synthase	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20240502	MGI			PMID:22617046
10297	Cbs	cystathionine beta-synthase	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20141030	MGI			PMID:25016930
10297	Cbs	cystathionine beta-synthase	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20141030	MGI			PMID:25016930
10297	Cbs	cystathionine beta-synthase	gene	MP:0010452	retina microaneurysm		IAGP		N	RGD:5509061	20141030	MGI			PMID:25016930
10297	Cbs	cystathionine beta-synthase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7878023
10297	Cbs	cystathionine beta-synthase	gene	MP:0011520	increased placental labyrinth size		IAGP		N	RGD:5509061	20240502	MGI			PMID:16984962
10297	Cbs	cystathionine beta-synthase	gene	MP:0012065	increased astrocyte number		IAGP		N	RGD:5509061	20141030	MGI			PMID:25016930
10297	Cbs	cystathionine beta-synthase	gene	MP:0012110	increased hair follicle number		IAGP		N	RGD:5509061	20181129	MGI			PMID:15386278
10297	Cbs	cystathionine beta-synthase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20161020	MGI			PMID:19204075
10297	Cbs	cystathionine beta-synthase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20161020	MGI			PMID:19858416
10297	Cbs	cystathionine beta-synthase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:15386278
10297	Cbs	cystathionine beta-synthase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:20566639
10297	Cbs	cystathionine beta-synthase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:7878023
10297	Cbs	cystathionine beta-synthase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:10993757
10297	Cbs	cystathionine beta-synthase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20220616	MGI			PMID:15622513
10297	Cbs	cystathionine beta-synthase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20240502	MGI			PMID:22617046
10297	Cbs	cystathionine beta-synthase	gene	MP:0012602	increased alpha-fetoprotein level		IAGP		N	RGD:5509061	20240502	MGI			PMID:22617046
10297	Cbs	cystathionine beta-synthase	gene	MP:0013022	increased Ly6C high monocyte number		IAGP		N	RGD:5509061	20161020	MGI			PMID:19858416
10297	Cbs	cystathionine beta-synthase	gene	MP:0014179	abnormal blood-retina barrier function		IAGP		N	RGD:5509061	20160526	MGI			PMID:25016930
10297	Cbs	cystathionine beta-synthase	gene	MP:0014682	increased polyploid hepatocyte number		IAGP		N	RGD:5509061	20250703	MGI			PMID:7878023
10297	Cbs	cystathionine beta-synthase	gene	MP:0030639	decreased circulating taurine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:20566639
10297	Cbs	cystathionine beta-synthase	gene	MP:0030644	increased circulating methionine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:19858416
10297	Cbs	cystathionine beta-synthase	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:7878023
10297	Cbs	cystathionine beta-synthase	gene	MP:0031214	hypercoagulability		IAGP		N	RGD:5509061	20201231	MGI			PMID:20638879
10298	Cck	cholecystokinin	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20161201	MGI			
10298	Cck	cholecystokinin	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330022
10298	Cck	cholecystokinin	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330022
10298	Cck	cholecystokinin	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20111116	MGI			
10299	Cckar	cholecystokinin A receptor	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15152034
10299	Cckar	cholecystokinin A receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10299	Cckar	cholecystokinin A receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459512
10299	Cckar	cholecystokinin A receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15168241
10299	Cckar	cholecystokinin A receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178543
10299	Cckar	cholecystokinin A receptor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459512
10299	Cckar	cholecystokinin A receptor	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10299	Cckar	cholecystokinin A receptor	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178543
10299	Cckar	cholecystokinin A receptor	gene	MP:0002646	increased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314689
10299	Cckar	cholecystokinin A receptor	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893936
10299	Cckar	cholecystokinin A receptor	gene	MP:0002830	gallstones		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314689
10299	Cckar	cholecystokinin A receptor	gene	MP:0002830	gallstones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927499
10299	Cckar	cholecystokinin A receptor	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10299	Cckar	cholecystokinin A receptor	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305161
10299	Cckar	cholecystokinin A receptor	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305161
10299	Cckar	cholecystokinin A receptor	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314689
10299	Cckar	cholecystokinin A receptor	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10299	Cckar	cholecystokinin A receptor	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459512
10299	Cckar	cholecystokinin A receptor	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305161
10299	Cckar	cholecystokinin A receptor	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314689
10299	Cckar	cholecystokinin A receptor	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10299	Cckar	cholecystokinin A receptor	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314689
10299	Cckar	cholecystokinin A receptor	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927499
10299	Cckar	cholecystokinin A receptor	gene	MP:0006002	abnormal small intestinal transit time		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314689
10299	Cckar	cholecystokinin A receptor	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15152034
10299	Cckar	cholecystokinin A receptor	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305161
10299	Cckar	cholecystokinin A receptor	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10299	Cckar	cholecystokinin A receptor	gene	MP:0009854	impaired gastric peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15168241
10299	Cckar	cholecystokinin A receptor	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20190502	MGI			
10299	Cckar	cholecystokinin A receptor	gene	MP:0020132	increased gallbladder volume		IAGP		N	RGD:5509061	20200116	MGI			PMID:15314689
10300	Cckbr	cholecystokinin B receptor	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20200514	MGI			
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459512
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15168241
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178543
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15325774
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459512
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013032
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15325774
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11403953
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11682252
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857893
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11682252
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15325774
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876222
10300	Cckbr	cholecystokinin B receptor	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178543
10300	Cckbr	cholecystokinin B receptor	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355324
10300	Cckbr	cholecystokinin B receptor	gene	MP:0002691	small stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876222
10300	Cckbr	cholecystokinin B receptor	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355324
10300	Cckbr	cholecystokinin B receptor	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392936
10300	Cckbr	cholecystokinin B receptor	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857893
10300	Cckbr	cholecystokinin B receptor	gene	MP:0003892	abnormal gastric gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978369
10300	Cckbr	cholecystokinin B receptor	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978369
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004152	abnormal circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755804
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004731	increased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15168241
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004731	increased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755804
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004731	increased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876222
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004731	increased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978369
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11682252
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459512
10300	Cckbr	cholecystokinin B receptor	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15325774
10300	Cckbr	cholecystokinin B receptor	gene	MP:0005218	abnormal pancreatic delta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978369
10300	Cckbr	cholecystokinin B receptor	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355324
10300	Cckbr	cholecystokinin B receptor	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978369
10300	Cckbr	cholecystokinin B receptor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857893
10300	Cckbr	cholecystokinin B receptor	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755804
10300	Cckbr	cholecystokinin B receptor	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11403953
10300	Cckbr	cholecystokinin B receptor	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925470
10300	Cckbr	cholecystokinin B receptor	gene	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11403953
10300	Cckbr	cholecystokinin B receptor	gene	MP:0009753	enhanced behavioral response to morphine		IAGP		N	RGD:5509061	20141003	MGI			PMID:11403953
10300	Cckbr	cholecystokinin B receptor	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:11403953
10300	Cckbr	cholecystokinin B receptor	gene	MP:0009854	impaired gastric peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15168241
10300	Cckbr	cholecystokinin B receptor	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876222
10300	Cckbr	cholecystokinin B receptor	gene	MP:0010803	abnormal stomach enteroendocrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978369
10300	Cckbr	cholecystokinin B receptor	gene	MP:0011891	decreased circulating ferritin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755804
10300	Cckbr	cholecystokinin B receptor	gene	MP:0011897	decreased circulating unsaturated transferrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755804
10300	Cckbr	cholecystokinin B receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857893
10300	Cckbr	cholecystokinin B receptor	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857893
10304	Cd2	CD2 antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:1358605
10306	Cd24a	CD24a antigen	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0010035	increased erythrocyte clearance		IAGP		N	RGD:5509061	20200618	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0014606	dark spleen		IAGP		N	RGD:5509061	20250206	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0020455	increased erythrocyte aggregation		IAGP		N	RGD:5509061	20170914	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0031063	increased erythrocyte sedimentation rate		IAGP		N	RGD:5509061	20200618	MGI			PMID:9028339
10306	Cd24a	CD24a antigen	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:9028339
10307	Cd28	CD28 antigen	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
10307	Cd28	CD28 antigen	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
10307	Cd28	CD28 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23793062
10307	Cd28	CD28 antigen	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7751626
10307	Cd28	CD28 antigen	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
10307	Cd28	CD28 antigen	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10477557
10307	Cd28	CD28 antigen	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
10307	Cd28	CD28 antigen	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725709
10307	Cd28	CD28 antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398586
10307	Cd28	CD28 antigen	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908623
10307	Cd28	CD28 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908623
10307	Cd28	CD28 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688139
10307	Cd28	CD28 antigen	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908623
10307	Cd28	CD28 antigen	gene	MP:0003278	esophageal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
10307	Cd28	CD28 antigen	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7751626
10307	Cd28	CD28 antigen	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467837
10307	Cd28	CD28 antigen	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528184
10307	Cd28	CD28 antigen	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285307
10307	Cd28	CD28 antigen	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
10307	Cd28	CD28 antigen	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10477557
10307	Cd28	CD28 antigen	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398586
10307	Cd28	CD28 antigen	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467837
10307	Cd28	CD28 antigen	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8808683
10307	Cd28	CD28 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
10307	Cd28	CD28 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688139
10307	Cd28	CD28 antigen	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23065717
10307	Cd28	CD28 antigen	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467837
10307	Cd28	CD28 antigen	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23065717
10307	Cd28	CD28 antigen	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23793062
10307	Cd28	CD28 antigen	gene	MP:0005002	abnormal T cell clonal deletion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342622
10307	Cd28	CD28 antigen	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17873878
10307	Cd28	CD28 antigen	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
10307	Cd28	CD28 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075933
10307	Cd28	CD28 antigen	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20141003	MGI			
10307	Cd28	CD28 antigen	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213110
10307	Cd28	CD28 antigen	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528184
10307	Cd28	CD28 antigen	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
10307	Cd28	CD28 antigen	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7751626
10307	Cd28	CD28 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285307
10307	Cd28	CD28 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
10307	Cd28	CD28 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908623
10307	Cd28	CD28 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
10307	Cd28	CD28 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398586
10307	Cd28	CD28 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23793062
10307	Cd28	CD28 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688139
10307	Cd28	CD28 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8808683
10307	Cd28	CD28 antigen	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467837
10307	Cd28	CD28 antigen	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:17873878
10307	Cd28	CD28 antigen	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
10307	Cd28	CD28 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10795741
10307	Cd28	CD28 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688139
10307	Cd28	CD28 antigen	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8808683
10307	Cd28	CD28 antigen	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8808683
10307	Cd28	CD28 antigen	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398586
10307	Cd28	CD28 antigen	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:10795741
10307	Cd28	CD28 antigen	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398586
10307	Cd28	CD28 antigen	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
10307	Cd28	CD28 antigen	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342622
10307	Cd28	CD28 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285307
10307	Cd28	CD28 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342622
10307	Cd28	CD28 antigen	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908623
10307	Cd28	CD28 antigen	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
10307	Cd28	CD28 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688139
10307	Cd28	CD28 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8808683
10307	Cd28	CD28 antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688139
10307	Cd28	CD28 antigen	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688139
10307	Cd28	CD28 antigen	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8808683
10307	Cd28	CD28 antigen	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23793062
10307	Cd28	CD28 antigen	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285307
10307	Cd28	CD28 antigen	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15629449
10307	Cd28	CD28 antigen	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15629449
10307	Cd28	CD28 antigen	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
10307	Cd28	CD28 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285307
10307	Cd28	CD28 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908623
10307	Cd28	CD28 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
10307	Cd28	CD28 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398586
10307	Cd28	CD28 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23793062
10307	Cd28	CD28 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688139
10307	Cd28	CD28 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7751626
10307	Cd28	CD28 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8808683
10307	Cd28	CD28 antigen	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
10307	Cd28	CD28 antigen	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8808683
10307	Cd28	CD28 antigen	gene	MP:0008747	abnormal T cell anergy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
10307	Cd28	CD28 antigen	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285307
10307	Cd28	CD28 antigen	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
10307	Cd28	CD28 antigen	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
10307	Cd28	CD28 antigen	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
10307	Cd28	CD28 antigen	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15629449
10308	Cd247	CD247 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688481
10308	Cd247	CD247 antigen	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223444
10308	Cd247	CD247 antigen	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223445
10308	Cd247	CD247 antigen	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10308	Cd247	CD247 antigen	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10308	Cd247	CD247 antigen	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10308	Cd247	CD247 antigen	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072519
10308	Cd247	CD247 antigen	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7520000
10308	Cd247	CD247 antigen	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223444
10308	Cd247	CD247 antigen	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072519
10308	Cd247	CD247 antigen	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7520000
10308	Cd247	CD247 antigen	gene	MP:0002433	abnormal T-helper 1 cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688481
10308	Cd247	CD247 antigen	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10308	Cd247	CD247 antigen	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0003080	increased natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11123272
10308	Cd247	CD247 antigen	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072519
10308	Cd247	CD247 antigen	gene	MP:0004165	abnormal lateral geniculate nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10308	Cd247	CD247 antigen	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10308	Cd247	CD247 antigen	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0005068	abnormal NK cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11123272
10308	Cd247	CD247 antigen	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021533
10308	Cd247	CD247 antigen	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223444
10308	Cd247	CD247 antigen	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072519
10308	Cd247	CD247 antigen	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688481
10308	Cd247	CD247 antigen	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223444
10308	Cd247	CD247 antigen	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223445
10308	Cd247	CD247 antigen	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223445
10308	Cd247	CD247 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IEA		N	RGD:5509061	20111208	MGI			
10308	Cd247	CD247 antigen	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10308	Cd247	CD247 antigen	gene	MP:0008036	abnormal NK T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072519
10308	Cd247	CD247 antigen	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7650493
10308	Cd247	CD247 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688481
10308	Cd247	CD247 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223444
10308	Cd247	CD247 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223445
10308	Cd247	CD247 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223444
10308	Cd247	CD247 antigen	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223445
10308	Cd247	CD247 antigen	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0008081	abnormal single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688481
10308	Cd247	CD247 antigen	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223444
10308	Cd247	CD247 antigen	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223445
10308	Cd247	CD247 antigen	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0008352	absent gamma-delta intraepithelial T cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10308	Cd247	CD247 antigen	gene	MP:0008356	abnormal gamma-delta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0008399	abnormal alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223445
10308	Cd247	CD247 antigen	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
10308	Cd247	CD247 antigen	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11123272
10308	Cd247	CD247 antigen	gene	MP:0008876	decreased uterine NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10308	Cd247	CD247 antigen	gene	MP:0008894	abnormal intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223444
10308	Cd247	CD247 antigen	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945921
10308	Cd247	CD247 antigen	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11123272
10308	Cd247	CD247 antigen	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8131747
10308	Cd247	CD247 antigen	gene	MP:0012529	abnormal decidua basalis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10308	Cd247	CD247 antigen	gene	MP:0012726	abnormal uterine spiral artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10308	Cd247	CD247 antigen	gene	MP:0012727	abnormal uterine spiral artery remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10308	Cd247	CD247 antigen	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:8223445
10308	Cd247	CD247 antigen	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:8223495
10308	Cd247	CD247 antigen	gene	MP:0013593	enlarged thymus cortex		IAGP		N	RGD:5509061	20150319	MGI			PMID:8223495
10309	Cd4	CD4 antigen	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521047
10309	Cd4	CD4 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551897
10309	Cd4	CD4 antigen	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9696828
10309	Cd4	CD4 antigen	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
10309	Cd4	CD4 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521047
10309	Cd4	CD4 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521047
10309	Cd4	CD4 antigen	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9696828
10309	Cd4	CD4 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486099
10309	Cd4	CD4 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15922720
10309	Cd4	CD4 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8500525
10309	Cd4	CD4 antigen	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551897
10309	Cd4	CD4 antigen	gene	MP:0002347	abnormal lymph node T cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521047
10309	Cd4	CD4 antigen	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8500525
10309	Cd4	CD4 antigen	gene	MP:0002408	abnormal double-positive T cell morphology		IEA		N	RGD:5509061	20220106	MGI			
10309	Cd4	CD4 antigen	gene	MP:0002418	increased susceptibility to viral infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7676644
10309	Cd4	CD4 antigen	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IEA		N	RGD:5509061	20220106	MGI			
10309	Cd4	CD4 antigen	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036949
10309	Cd4	CD4 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521047
10309	Cd4	CD4 antigen	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521047
10309	Cd4	CD4 antigen	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486099
10309	Cd4	CD4 antigen	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8467804
10309	Cd4	CD4 antigen	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521047
10309	Cd4	CD4 antigen	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:8500525
10309	Cd4	CD4 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017966
10309	Cd4	CD4 antigen	gene	MP:0004774	abnormal bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202343
10309	Cd4	CD4 antigen	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20210318	MGI			PMID:33238133
10309	Cd4	CD4 antigen	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725754
10309	Cd4	CD4 antigen	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725754
10309	Cd4	CD4 antigen	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668367
10309	Cd4	CD4 antigen	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24115907
10309	Cd4	CD4 antigen	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20111116	MGI			
10309	Cd4	CD4 antigen	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14688093
10309	Cd4	CD4 antigen	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8500525
10309	Cd4	CD4 antigen	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671660
10309	Cd4	CD4 antigen	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8500525
10309	Cd4	CD4 antigen	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551897
10309	Cd4	CD4 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748274
10309	Cd4	CD4 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8467804
10309	Cd4	CD4 antigen	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748274
10309	Cd4	CD4 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748274
10309	Cd4	CD4 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832488
10309	Cd4	CD4 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8467804
10309	Cd4	CD4 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671660
10309	Cd4	CD4 antigen	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748274
10309	Cd4	CD4 antigen	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8500525
10309	Cd4	CD4 antigen	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551897
10309	Cd4	CD4 antigen	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748274
10309	Cd4	CD4 antigen	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24115907
10309	Cd4	CD4 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748274
10309	Cd4	CD4 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14688093
10309	Cd4	CD4 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
10309	Cd4	CD4 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551897
10309	Cd4	CD4 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748274
10309	Cd4	CD4 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14688093
10309	Cd4	CD4 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832488
10309	Cd4	CD4 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
10309	Cd4	CD4 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8467804
10309	Cd4	CD4 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521047
10309	Cd4	CD4 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551897
10309	Cd4	CD4 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210318	MGI			PMID:33238133
10309	Cd4	CD4 antigen	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20210318	MGI			PMID:33238133
10309	Cd4	CD4 antigen	gene	MP:0008087	decreased T helper 1 cell number		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
10309	Cd4	CD4 antigen	gene	MP:0008100	absent plasma cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202343
10309	Cd4	CD4 antigen	gene	MP:0008345	abnormal gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8500525
10309	Cd4	CD4 antigen	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0008698	abnormal interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748274
10309	Cd4	CD4 antigen	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
10309	Cd4	CD4 antigen	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IAGP		N	RGD:5509061	20210318	MGI			PMID:33238133
10309	Cd4	CD4 antigen	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:8500525
10309	Cd4	CD4 antigen	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20141003	MGI			
10309	Cd4	CD4 antigen	gene	MP:0020191	abnormal lymphocyte activation involved in immune response		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
10309	Cd4	CD4 antigen	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:9696828
10310	Cd44	CD44 antigen	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0000336	decreased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19204665
10310	Cd44	CD44 antigen	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250474
10310	Cd44	CD44 antigen	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126101
10310	Cd44	CD44 antigen	gene	MP:0000362	decreased mast cell histamine storage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19204665
10310	Cd44	CD44 antigen	gene	MP:0000414	alopecia		IEA		N	RGD:5509061	20200430	MGI			
10310	Cd44	CD44 antigen	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825873
10310	Cd44	CD44 antigen	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16557236
10310	Cd44	CD44 antigen	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859330
10310	Cd44	CD44 antigen	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061657
10310	Cd44	CD44 antigen	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956084
10310	Cd44	CD44 antigen	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16557236
10310	Cd44	CD44 antigen	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16816384
10310	Cd44	CD44 antigen	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859330
10310	Cd44	CD44 antigen	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859330
10310	Cd44	CD44 antigen	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250474
10310	Cd44	CD44 antigen	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11935029
10310	Cd44	CD44 antigen	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342603
10310	Cd44	CD44 antigen	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11935029
10310	Cd44	CD44 antigen	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466136
10310	Cd44	CD44 antigen	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23318432
10310	Cd44	CD44 antigen	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20180712	MGI			PMID:22834956
10310	Cd44	CD44 antigen	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9310473
10310	Cd44	CD44 antigen	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
10310	Cd44	CD44 antigen	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:23318432
10310	Cd44	CD44 antigen	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528194
10310	Cd44	CD44 antigen	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585887
10310	Cd44	CD44 antigen	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15619667
10310	Cd44	CD44 antigen	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16557236
10310	Cd44	CD44 antigen	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16816384
10310	Cd44	CD44 antigen	gene	MP:0002936	joint swelling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12437588
10310	Cd44	CD44 antigen	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528194
10310	Cd44	CD44 antigen	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466136
10310	Cd44	CD44 antigen	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919379
10310	Cd44	CD44 antigen	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901064
10310	Cd44	CD44 antigen	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11762953
10310	Cd44	CD44 antigen	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16816384
10310	Cd44	CD44 antigen	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16098130
10310	Cd44	CD44 antigen	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16816384
10310	Cd44	CD44 antigen	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15596723
10310	Cd44	CD44 antigen	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20180712	MGI			PMID:22834956
10310	Cd44	CD44 antigen	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12437588
10310	Cd44	CD44 antigen	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16557236
10310	Cd44	CD44 antigen	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16816384
10310	Cd44	CD44 antigen	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901765
10310	Cd44	CD44 antigen	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23752202
10310	Cd44	CD44 antigen	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12437588
10310	Cd44	CD44 antigen	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528194
10310	Cd44	CD44 antigen	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972514
10310	Cd44	CD44 antigen	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9310473
10310	Cd44	CD44 antigen	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637488
10310	Cd44	CD44 antigen	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901765
10310	Cd44	CD44 antigen	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250474
10310	Cd44	CD44 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23752202
10310	Cd44	CD44 antigen	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11581304
10310	Cd44	CD44 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16098130
10310	Cd44	CD44 antigen	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859330
10310	Cd44	CD44 antigen	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859330
10310	Cd44	CD44 antigen	gene	MP:0005546	choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339747
10310	Cd44	CD44 antigen	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901765
10310	Cd44	CD44 antigen	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901765
10310	Cd44	CD44 antigen	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14551157
10310	Cd44	CD44 antigen	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16816384
10310	Cd44	CD44 antigen	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16098130
10310	Cd44	CD44 antigen	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9310473
10310	Cd44	CD44 antigen	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16816384
10310	Cd44	CD44 antigen	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825873
10310	Cd44	CD44 antigen	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
10310	Cd44	CD44 antigen	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
10310	Cd44	CD44 antigen	gene	MP:0008162	increased diameter of tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15619667
10310	Cd44	CD44 antigen	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15619667
10310	Cd44	CD44 antigen	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342603
10310	Cd44	CD44 antigen	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901064
10310	Cd44	CD44 antigen	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901064
10310	Cd44	CD44 antigen	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901064
10310	Cd44	CD44 antigen	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342603
10310	Cd44	CD44 antigen	gene	MP:0008591	increased circulating interleukin-1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0008599	increased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342603
10310	Cd44	CD44 antigen	gene	MP:0008651	increased interleukin-1 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901064
10310	Cd44	CD44 antigen	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901064
10310	Cd44	CD44 antigen	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901064
10310	Cd44	CD44 antigen	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16098130
10310	Cd44	CD44 antigen	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901064
10310	Cd44	CD44 antigen	gene	MP:0008800	increased small intestinal crypt cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483247
10310	Cd44	CD44 antigen	gene	MP:0008838	decreased transforming growth factor beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11935029
10310	Cd44	CD44 antigen	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23318432
10310	Cd44	CD44 antigen	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342603
10310	Cd44	CD44 antigen	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20160128	MGI			PMID:18854186
10310	Cd44	CD44 antigen	gene	MP:0009608	abnormal epidermal lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16557236
10310	Cd44	CD44 antigen	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342603
10310	Cd44	CD44 antigen	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11935029
10310	Cd44	CD44 antigen	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901064
10310	Cd44	CD44 antigen	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342603
10310	Cd44	CD44 antigen	gene	MP:0010677	decreased activation-induced cell death of T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342603
10310	Cd44	CD44 antigen	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0010842	decreased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
10310	Cd44	CD44 antigen	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
10310	Cd44	CD44 antigen	gene	MP:0010848	decreased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
10310	Cd44	CD44 antigen	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781582
10310	Cd44	CD44 antigen	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126101
10310	Cd44	CD44 antigen	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126101
10310	Cd44	CD44 antigen	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126101
10310	Cd44	CD44 antigen	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956084
10310	Cd44	CD44 antigen	gene	MP:0012434	decreased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483247
10310	Cd44	CD44 antigen	gene	MP:0012434	decreased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23318432
10310	Cd44	CD44 antigen	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
10310	Cd44	CD44 antigen	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23318432
10310	Cd44	CD44 antigen	gene	MP:0014373	increased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240328	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:17923692
10310	Cd44	CD44 antigen	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:16098130
10313	Cd53	CD53 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20180503	MGI			PMID:28487417
10314	Cd59a	CD59a antigen	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429844
10314	Cd59a	CD59a antigen	gene	MP:0000315	hemoglobinuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11435315
10314	Cd59a	CD59a antigen	gene	MP:0000332	hemoglobinemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11435315
10314	Cd59a	CD59a antigen	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14631387
10314	Cd59a	CD59a antigen	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11435315
10314	Cd59a	CD59a antigen	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17034582
10314	Cd59a	CD59a antigen	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296227
10314	Cd59a	CD59a antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296227
10314	Cd59a	CD59a antigen	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429844
10314	Cd59a	CD59a antigen	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17034582
10314	Cd59a	CD59a antigen	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:11986227
10314	Cd59a	CD59a antigen	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331407
10314	Cd59a	CD59a antigen	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:17034582
10314	Cd59a	CD59a antigen	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:19246097
10314	Cd59a	CD59a antigen	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11435315
10314	Cd59a	CD59a antigen	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15457473
10314	Cd59a	CD59a antigen	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959238
10314	Cd59a	CD59a antigen	gene	MP:0004041	increased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331407
10314	Cd59a	CD59a antigen	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331407
10314	Cd59a	CD59a antigen	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17034582
10314	Cd59a	CD59a antigen	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14631387
10314	Cd59a	CD59a antigen	gene	MP:0004823	increased susceptibility to experimental autoimmune myasthenia gravis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17034582
10314	Cd59a	CD59a antigen	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429844
10314	Cd59a	CD59a antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296227
10314	Cd59a	CD59a antigen	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19246097
10314	Cd59a	CD59a antigen	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959238
10314	Cd59a	CD59a antigen	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301611
10314	Cd59a	CD59a antigen	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19246097
10314	Cd59a	CD59a antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296227
10314	Cd59a	CD59a antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429844
10314	Cd59a	CD59a antigen	gene	MP:0005489	vascular smooth muscle hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959238
10314	Cd59a	CD59a antigen	gene	MP:0005546	choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17237428
10314	Cd59a	CD59a antigen	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429844
10314	Cd59a	CD59a antigen	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429844
10314	Cd59a	CD59a antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296227
10314	Cd59a	CD59a antigen	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17034582
10314	Cd59a	CD59a antigen	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:17034582
10314	Cd59a	CD59a antigen	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429844
10314	Cd59a	CD59a antigen	gene	MP:0010653	abnormal Wallerian degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19246097
10314	Cd59a	CD59a antigen	gene	MP:0020929	decreased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16301611
10314	Cd59a	CD59a antigen	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17429844
10314	Cd59a	CD59a antigen	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:11435315
10316	Cd80	CD80 antigen	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12207354
10316	Cd80	CD80 antigen	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075931
10316	Cd80	CD80 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075931
10316	Cd80	CD80 antigen	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10477557
10316	Cd80	CD80 antigen	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075931
10316	Cd80	CD80 antigen	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10453003
10316	Cd80	CD80 antigen	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11169445
10316	Cd80	CD80 antigen	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075931
10316	Cd80	CD80 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075931
10316	Cd80	CD80 antigen	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10453003
10316	Cd80	CD80 antigen	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10795741
10316	Cd80	CD80 antigen	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10795741
10316	Cd80	CD80 antigen	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16886063
10316	Cd80	CD80 antigen	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12207354
10316	Cd80	CD80 antigen	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10477557
10316	Cd80	CD80 antigen	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12207354
10316	Cd80	CD80 antigen	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10795741
10316	Cd80	CD80 antigen	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16886063
10316	Cd80	CD80 antigen	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16886063
10316	Cd80	CD80 antigen	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16886063
10316	Cd80	CD80 antigen	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23793062
10316	Cd80	CD80 antigen	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725709
10316	Cd80	CD80 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7694362
10316	Cd80	CD80 antigen	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10453003
10316	Cd80	CD80 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10477557
10316	Cd80	CD80 antigen	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10453003
10316	Cd80	CD80 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10795741
10316	Cd80	CD80 antigen	gene	MP:0005623	abnormal meninges morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12207354
10316	Cd80	CD80 antigen	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725709
10316	Cd80	CD80 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075931
10316	Cd80	CD80 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075931
10316	Cd80	CD80 antigen	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075931
10316	Cd80	CD80 antigen	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10477557
10316	Cd80	CD80 antigen	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10477557
10316	Cd80	CD80 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12207354
10316	Cd80	CD80 antigen	gene	MP:0009023	abnormal spinal cord meninges morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12207354
10317	Cd8a	CD8 subunit alpha	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20180719	MGI			PMID:1673361
10317	Cd8a	CD8 subunit alpha	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20180719	MGI			PMID:9696828
10317	Cd8a	CD8 subunit alpha	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20180719	MGI			PMID:11114377
10317	Cd8a	CD8 subunit alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:15922720
10317	Cd8a	CD8 subunit alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:8500525
10317	Cd8a	CD8 subunit alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:12049715
10317	Cd8a	CD8 subunit alpha	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8500525
10317	Cd8a	CD8 subunit alpha	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17082573
10317	Cd8a	CD8 subunit alpha	gene	MP:0002418	increased susceptibility to viral infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:7676644
10317	Cd8a	CD8 subunit alpha	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:22036949
10317	Cd8a	CD8 subunit alpha	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20180719	MGI			PMID:15729333
10317	Cd8a	CD8 subunit alpha	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20180719	MGI			PMID:17082573
10317	Cd8a	CD8 subunit alpha	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IEA		N	RGD:5509061	20180719	MGI			
10317	Cd8a	CD8 subunit alpha	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20180719	MGI			PMID:8500525
10317	Cd8a	CD8 subunit alpha	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20180719	MGI			PMID:17082573
10317	Cd8a	CD8 subunit alpha	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17873878
10317	Cd8a	CD8 subunit alpha	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9806635
10317	Cd8a	CD8 subunit alpha	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:1673361
10317	Cd8a	CD8 subunit alpha	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20180719	MGI			PMID:8500525
10317	Cd8a	CD8 subunit alpha	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8500525
10317	Cd8a	CD8 subunit alpha	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20180719	MGI			PMID:14525595
10317	Cd8a	CD8 subunit alpha	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8500525
10317	Cd8a	CD8 subunit alpha	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:17082573
10317	Cd8a	CD8 subunit alpha	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:12049716
10317	Cd8a	CD8 subunit alpha	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:17082573
10317	Cd8a	CD8 subunit alpha	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20220106	MGI			
10317	Cd8a	CD8 subunit alpha	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20220106	MGI			
10317	Cd8a	CD8 subunit alpha	gene	MP:0008345	abnormal gamma-delta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8500525
10317	Cd8a	CD8 subunit alpha	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0011822	increased CD8-positive, alpha-beta memory T cell proliferation		IEA		N	RGD:5509061	20180719	MGI			
10317	Cd8a	CD8 subunit alpha	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20180719	MGI			PMID:8500525
10317	Cd8a	CD8 subunit alpha	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180719	MGI			PMID:21964024
10317	Cd8a	CD8 subunit alpha	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
10317	Cd8a	CD8 subunit alpha	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:9696828
10320	Cdh6	cadherin 6	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10864459
10320	Cdh6	cadherin 6	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10864459
10320	Cdh6	cadherin 6	gene	MP:0011291	nephron necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10864459
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19061836
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23266956
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:22113502
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20220303	MGI			PMID:19079609
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044451
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899789
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20170817	MGI			PMID:21804542
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368906
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368906
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398955
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16620915
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22772081
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20160331	MGI			PMID:25252692
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22772081
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22113502
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22113502
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544530
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681207
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899789
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585505
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467612
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160331	MGI			PMID:25252692
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16620915
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339492
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339492
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:16620915
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987514
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339492
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20211104	MGI			PMID:26240281
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001885	mammary gland duct hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044451
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924978
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398955
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851974
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339492
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339492
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681207
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465598
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544530
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368906
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665695
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16015333
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17114584
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9624006
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16015333
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16015333
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23565506
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20171116	MGI			PMID:11751631
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20171116	MGI			PMID:21118965
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141120	MGI			PMID:16540681
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20160929	MGI			PMID:23858101
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544530
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665695
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16015333
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676052
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20160929	MGI			PMID:23858101
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20170420	MGI			PMID:26987019
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368906
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489287
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20160929	MGI			PMID:23858101
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20170420	MGI			PMID:26987019
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002037	increased fibrohistocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544530
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23845441
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158963
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313388
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670909
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16015333
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158963
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438529
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19079609
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398955
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805356
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22113502
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465598
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23845441
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20180222	MGI			PMID:28652370
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:19339492
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037818
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044451
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20180222	MGI			PMID:28652370
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003155	abnormal telomere length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339492
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11551927
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003570	increased uterus leiomyoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20220303	MGI			PMID:19079609
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665695
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16015333
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23266956
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11551927
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20211104	MGI			PMID:26240281
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11551927
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544530
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713536
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19345328
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665695
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987514
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713536
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20180222	MGI			PMID:28652370
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339492
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20180222	MGI			PMID:28652370
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005195	abnormal posterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16620915
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:22113502
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11551927
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16620915
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11551927
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0005623	abnormal meninges morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924978
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16620915
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0006148	binocular blindness		IAGP		N	RGD:5509061	20180222	MGI			PMID:28652370
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:28652370
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11551927
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299132
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20171116	MGI			PMID:11751631
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924978
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009043	increased pancreas adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22113502
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681207
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585505
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17114584
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22611036
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467612
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681207
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22113502
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681207
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585505
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22113502
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467612
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19079609
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20639864
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22113502
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009319	increased small lymphocytic lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665695
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009459	skeletal muscle hyperplasia		IAGP		N	RGD:5509061	20170420	MGI			PMID:26987019
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044451
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009515	increased gastrointestinal stromal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665695
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11551927
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009621	primary vitreous hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037818
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009621	primary vitreous hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465598
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010273	increased classified tumor incidence		IAGP		N	RGD:5509061	20141120	MGI			PMID:16540681
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544530
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368906
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902988
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19345328
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398955
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048081
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20160114	MGI			PMID:25705882
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010276	increased intraocular melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987514
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670909
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438529
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851974
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713536
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17114584
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670909
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010309	increased mesothelioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010310	increased Schwannoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010311	increased meningioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924978
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010311	increased meningioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010312	increased oligodendroglioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670909
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010312	increased oligodendroglioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438529
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010312	increased oligodendroglioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805356
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010313	increased osteoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924978
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010322	increased cutaneous melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899789
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010322	increased cutaneous melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22772081
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010322	increased cutaneous melanoma incidence		IAGP		N	RGD:5509061	20141120	MGI			PMID:16540681
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010322	increased cutaneous melanoma incidence		IAGP		N	RGD:5509061	20160331	MGI			PMID:25252692
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010322	increased cutaneous melanoma incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:22983396
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010334	pleural effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010336	increased acute lymphoblastic leukemia incidence		IAGP		N	RGD:5509061	20180222	MGI			PMID:28652370
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010347	osseous metaplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924978
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:16620915
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465598
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20180222	MGI			PMID:28652370
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010727	increased glioblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196966
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0010741	abnormal melanocyte proliferation		IAGP		N	RGD:5509061	20160331	MGI			PMID:25252692
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20211104	MGI			PMID:26240281
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:15044451
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:8620534
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0011748	intestinal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0012193	increased keratinocyte migration		IAGP		N	RGD:5509061	20141204	MGI			PMID:21970857
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544530
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665695
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16015333
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393858
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:17360455
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:14681207
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:14724566
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:17114584
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:19196966
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:20697345
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23467612
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0014660	increased skin nevi incidence		IAGP		N	RGD:5509061	20250508	MGI			PMID:19345328
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0014660	increased skin nevi incidence		IAGP		N	RGD:5509061	20250508	MGI			PMID:25252692
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:11891301
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:16620915
10322	Cdkn2a	cyclin dependent kinase inhibitor 2A	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:19339492
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982846
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974039
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22715416
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589173
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672531
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589173
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17290224
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17290224
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22715416
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974039
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001345	Meibomian gland atrophy		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982846
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974039
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516642
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974039
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17290224
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589173
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22715416
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001603	failure of myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589173
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982846
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672531
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15130516
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001934	increased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638888
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9315660
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672531
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589173
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15130516
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22715416
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672531
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589173
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428455
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11683182
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002274	abnormal type I pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22715416
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672531
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516642
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002717	abnormal male preputial gland morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516642
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982846
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982846
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22715416
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0003326	liver failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638888
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516642
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638888
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516642
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11683182
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22715416
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005044	sepsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589173
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974039
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005252	abnormal Meibomian gland morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17290224
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672531
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516642
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17290224
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516642
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982846
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0008991	abnormal bile canaliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982846
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17290224
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638888
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:17290224
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20150611	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010682	abnormal hair follicle infundibulum morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010688	hair follicle outer root sheath hyperplasia		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11683182
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010812	absent type II pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010814	absent alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010817	absent type I pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010817	absent type I pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0010903	abnormal pulmonary alveolus wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11683182
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394553
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467360
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8798745
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982846
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0013375	abnormal sebocyte morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0013376	abnormal sebocyte differentiation		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0013723	increased circulating tyrosine level		IAGP		N	RGD:5509061	20150409	MGI			PMID:7652557
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0014473	increased pulmonary alveolus wall thickness		IAGP		N	RGD:5509061	20240704	MGI			PMID:16428462
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:17290224
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:15319454
10325	Cebpa	CCAAT/enhancer binding protein alpha	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:17290224
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727068
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20047998
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637691
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637692
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637691
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637692
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9303532
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9303532
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20171228	MGI			PMID:15762841
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001345	Meibomian gland atrophy		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20171228	MGI			PMID:15762841
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001553	abnormal circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20171228	MGI			PMID:15762841
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7530603
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637691
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9303532
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637692
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756662
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727068
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20047998
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002343	abnormal lymph node cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002346	abnormal lymph node secondary follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002347	abnormal lymph node T cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002348	abnormal lymph node medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002377	abnormal mucosa-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180906	MGI			PMID:28476751
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911624
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7530603
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002421	abnormal cell-mediated immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911624
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7530603
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911624
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002715	decreased glycogen catabolism rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002717	abnormal male preputial gland morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002742	enlarged submandibular lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805133
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003356	impaired luteinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9303532
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9303532
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727068
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756662
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:24885110
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756662
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16205634
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805133
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:24885110
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004817	abnormal skeletal muscle mass		IAGP		N	RGD:5509061	20170202	MGI			PMID:24885110
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20047998
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20047998
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005252	abnormal Meibomian gland morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:24885110
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20171228	MGI			PMID:15762841
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911624
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20047998
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727068
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20171228	MGI			PMID:15762841
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008472	abnormal spleen secondary B follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180906	MGI			PMID:28476751
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20180906	MGI			PMID:28476751
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20047998
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20180906	MGI			PMID:28476751
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008618	decreased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724128
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911624
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177475
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008838	decreased transforming growth factor beta level		IAGP		N	RGD:5509061	20180906	MGI			PMID:28476751
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805133
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:9531536
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9303532
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009112	abnormal pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009134	abnormal brown fat lipid droplet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20171228	MGI			PMID:15762841
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009307	decreased uterine fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916132
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20047998
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805133
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805133
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009488	abnormal pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637692
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756662
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16205634
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009623	enlarged inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009631	enlarged axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180906	MGI			PMID:28476751
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0010172	abnormal mammary gland epithelium physiology		IAGP		N	RGD:5509061	20150611	MGI			PMID:9637692
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0010682	abnormal hair follicle infundibulum morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0010688	hair follicle outer root sheath hyperplasia		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20047998
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20171228	MGI			PMID:15762841
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7530603
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19749746
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7530603
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9303532
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011224	abnormal lymph node medullary cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7744000
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011579	decreased lipoprotein lipase activity		IAGP		N	RGD:5509061	20171228	MGI			PMID:15762841
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20171228	MGI			PMID:15762841
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805133
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0013375	abnormal sebocyte morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0013376	abnormal sebocyte differentiation		IAGP		N	RGD:5509061	20150813	MGI			PMID:20352127
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0013661	abnormal myeloid cell number		IAGP		N	RGD:5509061	20180906	MGI			PMID:28476751
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0014998	abnormal glucose metabolism		IAGP		N	RGD:5509061	20260611	MGI			PMID:10747954
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0020080	increased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:19440205
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:9303532
10326	Cebpb	CCAAT/enhancer binding protein beta	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:10747954
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:12626772
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724803
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177475
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177475
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177475
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177475
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0008822	decreased blood uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873376
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0009134	abnormal brown fat lipid droplet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12626772
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873376
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0009810	increased urine uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873376
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0010173	increased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12626772
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405372
10327	Cebpd	CCAAT/enhancer binding protein delta	gene	MP:0013404	decreased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:16873376
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0001602	impaired myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0001867	rhinitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0002443	abnormal eosinophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0005190	osteomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371821
10328	Cebpe	CCAAT/enhancer binding protein epsilon	gene	MP:0031053	pleuritis		IAGP		N	RGD:5509061	20200618	MGI			PMID:9371821
10329	Cebpg	CCAAT/enhancer binding protein gamma	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587348
10329	Cebpg	CCAAT/enhancer binding protein gamma	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587348
10329	Cebpg	CCAAT/enhancer binding protein gamma	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587348
10329	Cebpg	CCAAT/enhancer binding protein gamma	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587348
10330	Cel	carboxyl ester lipase	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
10330	Cel	carboxyl ester lipase	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
10330	Cel	carboxyl ester lipase	gene	MP:0003334	pancreas fibrosis		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
10330	Cel	carboxyl ester lipase	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
10330	Cel	carboxyl ester lipase	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
10330	Cel	carboxyl ester lipase	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
10330	Cel	carboxyl ester lipase	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10194330
10330	Cel	carboxyl ester lipase	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
10330	Cel	carboxyl ester lipase	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:8636157
10330	Cel	carboxyl ester lipase	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
10330	Cel	carboxyl ester lipase	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
10330	Cel	carboxyl ester lipase	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0009150	pancreatic acinar cell atrophy		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0013220	increased pancreas apoptosis		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0013295	pancreas atrophy		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10330	Cel	carboxyl ester lipase	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20251106	MGI			PMID:35398595
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20160519	MGI			PMID:15246977
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519339
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921521
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7482032
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000494	abnormal cecum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7527588
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1382232
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001135	abnormal uterine cervix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540910
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1382232
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180830	MGI			PMID:29924856
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921521
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7556083
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180830	MGI			PMID:29924856
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7482032
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20220505	MGI			PMID:35392567
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823443
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7482032
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7556083
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160519	MGI			PMID:15246977
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160519	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160519	MGI			PMID:18802965
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001765	abnormal ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001784	abnormal fluid regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921521
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10570187
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15246977
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540910
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519339
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7482032
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519339
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7482032
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0001947	abnormal mucociliary clearance		IAGP		N	RGD:5509061	20151224	MGI			PMID:22937152
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:1355249
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802965
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7482032
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160519	MGI			PMID:7545494
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180830	MGI			PMID:29924856
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220505	MGI			PMID:35392567
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823443
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002163	abnormal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002163	abnormal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802965
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002238	abnormal nasal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002240	abnormal paranasal sinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002309	abnormal vital capacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20151224	MGI			PMID:22937152
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540910
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519339
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1382232
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003251	gallbladder inflammation		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:1355249
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15246977
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571105
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7482032
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20160519	MGI			PMID:18802965
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20160519	MGI			PMID:7545494
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20180830	MGI			PMID:29924856
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20220505	MGI			PMID:35392567
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20160519	MGI			PMID:7545494
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003340	acute pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003426	pulmonary interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823443
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802965
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711878
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7527588
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7556083
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20220505	MGI			PMID:35392567
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003666	impaired sperm capacitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519339
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17506901
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10570187
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711878
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:7545494
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7556083
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:7545494
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0005084	abnormal gallbladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0005085	abnormal gallbladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7556083
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:15246977
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180830	MGI			PMID:29924856
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17947234
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20220505	MGI			PMID:35392567
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325992
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009150	pancreatic acinar cell atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009161	pancreatic acinar cell zymogen granule accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10570187
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009342	enlarged gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009342	enlarged gallbladder		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009343	dilated gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009477	small cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:1355249
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009478	coiled cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009478	coiled cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:7527588
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009484	ileum hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10570187
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20160519	MGI			PMID:15246977
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20160519	MGI			PMID:11102538
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20160519	MGI			PMID:7545494
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0010156	abnormal small intestinal crypt cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711878
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0010156	abnormal small intestinal crypt cell physiology		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571105
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0010858	pulmonary epithelial necrosis		IAGP		N	RGD:5509061	20151224	MGI			PMID:22937152
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0010861	increased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0010861	increased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540910
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1355249
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7527588
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7949729
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151224	MGI			PMID:22937152
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160519	MGI			PMID:11102538
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160519	MGI			PMID:18802965
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160519	MGI			PMID:7545494
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220505	MGI			PMID:35392567
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0012518	abnormal Brunner's gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0012519	dilated Brunner's gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:7560099
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0013455	lacrimal gland atrophy		IAGP		N	RGD:5509061	20150205	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0013494	abnormal trachea gland morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:1380723
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0013792	abnormal small intestine goblet cell morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:7527588
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0013797	abnormal ileal goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:16571105
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014028	decreased respiratory epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160519	MGI			PMID:15246977
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014028	decreased respiratory epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160519	MGI			PMID:18802965
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014028	decreased respiratory epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160519	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014028	decreased respiratory epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160519	MGI			PMID:7545494
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014028	decreased respiratory epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160519	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014028	decreased respiratory epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:1382232
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014028	decreased respiratory epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:7556083
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014028	decreased respiratory epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014028	decreased respiratory epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:9399953
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014033	abnormal submucosal gland morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014036	meconium ileus		IAGP		N	RGD:5509061	20160519	MGI			PMID:7545494
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014036	meconium ileus		IAGP		N	RGD:5509061	20160519	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014036	meconium ileus		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014036	meconium ileus		IAGP		N	RGD:5509061	20160526	MGI			PMID:1355249
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014036	meconium ileus		IAGP		N	RGD:5509061	20160526	MGI			PMID:7949729
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014079	decreased small intestinal villus number		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014182	decreased respiratory epithelial sodium ion transmembrane transport		IAGP		N	RGD:5509061	20160519	MGI			PMID:15246977
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014182	decreased respiratory epithelial sodium ion transmembrane transport		IAGP		N	RGD:5509061	20160519	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014182	decreased respiratory epithelial sodium ion transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014183	increased respiratory epithelial sodium ion transmembrane transport		IAGP		N	RGD:5509061	20160519	MGI			PMID:8589719
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014206	decreased intestinal epithelial sodium ion transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014208	decreased intestinal epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:1382232
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014208	decreased intestinal epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:18802965
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014208	decreased intestinal epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014208	decreased intestinal epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:7527588
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014208	decreased intestinal epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:7556083
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014226	abnormal alveolar macrophage physiology		IAGP		N	RGD:5509061	20160526	MGI			PMID:16921366
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014230	dilated crypt of Lieberkuhn		IAGP		N	RGD:5509061	20160526	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014230	dilated crypt of Lieberkuhn		IAGP		N	RGD:5509061	20160526	MGI			PMID:7527588
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014230	dilated crypt of Lieberkuhn		IAGP		N	RGD:5509061	20160526	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014230	dilated crypt of Lieberkuhn		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014230	dilated crypt of Lieberkuhn		IAGP		N	RGD:5509061	20220505	MGI			PMID:35392567
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014231	intestinal mucus accumulation		IAGP		N	RGD:5509061	20160526	MGI			PMID:18802965
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014231	intestinal mucus accumulation		IAGP		N	RGD:5509061	20160526	MGI			PMID:7505691
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014231	intestinal mucus accumulation		IAGP		N	RGD:5509061	20160526	MGI			PMID:7685652
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014232	dilated pancreatic acinus		IAGP		N	RGD:5509061	20160526	MGI			PMID:10570187
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0014233	bile duct epithelium hyperplasia		IAGP		N	RGD:5509061	20160526	MGI			PMID:8605891
10331	Cftr	cystic fibrosis transmembrane conductance regulator	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220303	MGI			PMID:18325992
10339	Chga	chromogranin A	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0002909	abnormal adrenal gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0005662	increased circulating adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0005665	increased circulating noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0011478	abnormal urine catecholamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556729
10339	Chga	chromogranin A	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:16007257
10339	Chga	chromogranin A	gene	MP:0030762	decreased adrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:16007257
10340	Chgb	chromogranin B	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089903
10340	Chgb	chromogranin B	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20126668
10340	Chgb	chromogranin B	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20126668
10340	Chgb	chromogranin B	gene	MP:0008504	abnormal adrenal chromaffin cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089903
10340	Chgb	chromogranin B	gene	MP:0010147	abnormal endocrine pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20126668
10340	Chgb	chromogranin B	gene	MP:0030762	decreased adrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:20089903
10343	Chm	CHM Rab escort protein	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175730
10343	Chm	CHM Rab escort protein	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410831
10343	Chm	CHM Rab escort protein	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175730
10343	Chm	CHM Rab escort protein	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242790
10343	Chm	CHM Rab escort protein	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0014666	abnormal Muller cell physiology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0020359	abnormal ribbon synapse morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10343	Chm	CHM Rab escort protein	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20260521	MGI			PMID:41429839
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11961069
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468635
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729838
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147565
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382674
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0001629	abnormal heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688600
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147565
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919709
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0002822	catalepsy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147565
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0002917	decreased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919709
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147565
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16110248
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0005085	abnormal gallbladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11961069
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729838
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147565
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147565
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147565
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147565
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:16110248
10353	Chrm4	cholinergic receptor, muscarinic 4	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:10468635
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964949
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226318
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964949
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226318
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964949
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15963492
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:10235262
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17146052
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10235262
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15963492
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15963492
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12623222
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964949
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226318
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12623222
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17146052
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964949
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17146052
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0003996	clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17146052
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12623222
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17146052
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20061993
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0008035	behavioral arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17146052
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009475	abnormal nicotine-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:10235262
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20061993
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009713	enhanced conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528443
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964949
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881519
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20061993
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226318
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009752	enhanced behavioral response to nicotine		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226318
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009752	enhanced behavioral response to nicotine		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528443
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009752	enhanced behavioral response to nicotine		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009756	impaired behavioral response to nicotine		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881519
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0009756	impaired behavioral response to nicotine		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226318
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226318
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0014625	abnormal ictal brain wave pattern		IAGP		N	RGD:5509061	20251204	MGI			PMID:17146052
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0031334	increased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:17146052
10355	Chrna4	cholinergic receptor, nicotinic, alpha polypeptide 4	gene	MP:0031753	increased inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20260813	MGI			PMID:17146052
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083057
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10800961
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24983521
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10800961
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20141003	MGI			PMID:11834293
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001054	failure of neuromuscular synapse presynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498043
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10454356
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541879
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541879
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10800961
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10800961
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10454356
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15963492
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364063
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15364017
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15364017
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10800961
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364063
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150409	MGI			PMID:24879866
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0002414	abnormal myeloblast morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083057
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15963492
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15944242
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20128845
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10800961
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24983521
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0003450	enlarged pancreas		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201231	MGI			
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541879
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541879
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20141120	MGI			PMID:24983521
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24983521
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20141120	MGI			PMID:24983521
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083057
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0006408	dorsal root ganglion hypoplasia		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141120	MGI			PMID:20713028
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12508119
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12508119
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15364017
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0009475	abnormal nicotine-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:10800961
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0009475	abnormal nicotine-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364063
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0009516	enlarged salivary gland		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24983521
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10800961
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0011114	abnormal airway basal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808646
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0011115	airway basal cell hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808646
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083057
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24983521
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0012174	flat head		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0012709	delayed caudal neuropore closure		IAGP		N	RGD:5509061	20151001	MGI			PMID:22473653
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:16923147
10357	Chrna7	cholinergic receptor, nicotinic, alpha polypeptide 7	gene	MP:0030091	macrodontia		IAGP		N	RGD:5509061	20171005	MGI			PMID:22473653
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20240523	MGI			
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959719
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20240523	MGI			
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20240523	MGI			
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0001785	edema		IEA		N	RGD:5509061	20240523	MGI			
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20240523	MGI			
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20240523	MGI			
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959719
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
10358	Chrnb1	cholinergic receptor nicotinic beta 1 subunit	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20240523	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639173
10364	Ckb	creatine kinase, brain	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639173
10364	Ckb	creatine kinase, brain	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12059977
10364	Ckb	creatine kinase, brain	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639173
10364	Ckb	creatine kinase, brain	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12059977
10364	Ckb	creatine kinase, brain	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639173
10364	Ckb	creatine kinase, brain	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639173
10364	Ckb	creatine kinase, brain	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639173
10364	Ckb	creatine kinase, brain	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20181227	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639173
10364	Ckb	creatine kinase, brain	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12059977
10364	Ckb	creatine kinase, brain	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639173
10364	Ckb	creatine kinase, brain	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12059977
10364	Ckb	creatine kinase, brain	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639173
10364	Ckb	creatine kinase, brain	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
10364	Ckb	creatine kinase, brain	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
10367	Clps	colipase, pancreatic	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622781
10367	Clps	colipase, pancreatic	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622781
10367	Clps	colipase, pancreatic	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0002791	steatorrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622781
10367	Clps	colipase, pancreatic	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751900
10367	Clps	colipase, pancreatic	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10367	Clps	colipase, pancreatic	gene	MP:0030531	abnormal facial skin morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:11751900
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16421286
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611851
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611851
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611851
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16421286
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611851
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20160421	MGI			
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16421286
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611851
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16421286
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16421286
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16421286
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611851
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20150122	MGI			PMID:22917771
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20150122	MGI			PMID:24641901
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20250508	MGI			
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150122	MGI			PMID:24641901
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611851
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611851
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0011464	bilirubinuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611851
10368	Abcc2	ATP-binding cassette, sub-family C member 2	gene	MP:0011464	bilirubinuria		IAGP		N	RGD:5509061	20150122	MGI			PMID:22917771
10370	Cnr1	cannabinoid receptor 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908955
10370	Cnr1	cannabinoid receptor 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525344
10370	Cnr1	cannabinoid receptor 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719095
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770190
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406230
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823890
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:15078564
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823890
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12405999
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15078564
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888857
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318961
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318962
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406230
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888857
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12152079
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:18256258
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571781
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406230
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833324
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15078564
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060781
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:12152079
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318961
10370	Cnr1	cannabinoid receptor 1	gene	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719095
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12152079
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318961
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406230
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15078564
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770190
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318962
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002798	abnormal active avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823890
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002822	catalepsy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318961
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770190
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526074
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908411
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060781
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002917	decreased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002918	abnormal paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12152079
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734603
10370	Cnr1	cannabinoid receptor 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908411
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10619457
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12152079
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318961
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:12427832
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823890
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:19607846
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888857
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21050275
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080779
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833324
10370	Cnr1	cannabinoid receptor 1	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21050275
10370	Cnr1	cannabinoid receptor 1	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406230
10370	Cnr1	cannabinoid receptor 1	gene	MP:0004209	abnormal sweet taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080779
10370	Cnr1	cannabinoid receptor 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719095
10370	Cnr1	cannabinoid receptor 1	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719095
10370	Cnr1	cannabinoid receptor 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
10370	Cnr1	cannabinoid receptor 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15266010
10370	Cnr1	cannabinoid receptor 1	gene	MP:0005131	increased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833324
10370	Cnr1	cannabinoid receptor 1	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833324
10370	Cnr1	cannabinoid receptor 1	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833324
10370	Cnr1	cannabinoid receptor 1	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770190
10370	Cnr1	cannabinoid receptor 1	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719666
10370	Cnr1	cannabinoid receptor 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770190
10370	Cnr1	cannabinoid receptor 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770190
10370	Cnr1	cannabinoid receptor 1	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12427832
10370	Cnr1	cannabinoid receptor 1	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12427832
10370	Cnr1	cannabinoid receptor 1	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526074
10370	Cnr1	cannabinoid receptor 1	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318961
10370	Cnr1	cannabinoid receptor 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318961
10370	Cnr1	cannabinoid receptor 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406230
10370	Cnr1	cannabinoid receptor 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719095
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21050275
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009710	anhedonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823890
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888857
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917492
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318961
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888857
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888857
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12427832
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526074
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
10370	Cnr1	cannabinoid receptor 1	gene	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719095
10370	Cnr1	cannabinoid receptor 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770190
10370	Cnr1	cannabinoid receptor 1	gene	MP:0010119	abnormal bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908955
10370	Cnr1	cannabinoid receptor 1	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20141003	MGI			PMID:19607846
10370	Cnr1	cannabinoid receptor 1	gene	MP:0011082	abnormal gastrointestinal motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22836266
10370	Cnr1	cannabinoid receptor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10318961
10370	Cnr1	cannabinoid receptor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
10370	Cnr1	cannabinoid receptor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10370	Cnr1	cannabinoid receptor 1	gene	MP:0012009	early parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833324
10370	Cnr1	cannabinoid receptor 1	gene	MP:0014440	increased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:12060781
10370	Cnr1	cannabinoid receptor 1	gene	MP:0014440	increased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:14770190
10370	Cnr1	cannabinoid receptor 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
10370	Cnr1	cannabinoid receptor 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:9888857
10370	Cnr1	cannabinoid receptor 1	gene	MP:0031426	increased sperm motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:17395184
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20181227	MGI			
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581026
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0003393	decreased cardiac output		IEA		N	RGD:5509061	20210128	MGI			
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0004591	enlarged tectorial membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581026
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581026
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0004749	nonsyndromic hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581026
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581026
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220519	MGI			
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0011896	increased circulating unsaturated transferrin level		IEA		N	RGD:5509061	20211021	MGI			
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581026
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0012546	triangular face		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668593
10371	Col11a2	collagen, type XI, alpha 2	gene	MP:0030049	prominent forehead		IAGP		N	RGD:5509061	20170921	MGI			PMID:11668593
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334604
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334604
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334604
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334604
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334604
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334604
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334604
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0010225	abnormal quadriceps morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334604
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334604
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160616	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:21670218
10372	Col12a1	collagen, type XII, alpha 1	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20190704	MGI			PMID:21670218
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000103	nasal bone hypoplasia		IAGP		N	RGD:5509061	20171026	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21917142
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832566
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8989518
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832566
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180503	MGI			PMID:26545783
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20171026	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000533	kidney hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8989518
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20180503	MGI			PMID:26545783
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000550	abnormal forelimb morphology		IEA		N	RGD:5509061	20111116	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000556	abnormal hindlimb morphology		IEA		N	RGD:5509061	20111116	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8192242
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968670
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20141003	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968670
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180503	MGI			PMID:26545783
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546167
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968670
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968670
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001411	spinning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968670
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968670
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001942	abnormal lung volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:8192242
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:8192242
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968670
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22248926
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151112	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8192242
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20180503	MGI			PMID:26545783
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004134	abnormal chest morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004134	abnormal chest morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004134	abnormal chest morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004282	retrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004356	radius hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26545783
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004667	vertebral body hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004669	enlarged vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004669	enlarged vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8192242
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832566
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20141003	MGI			PMID:8989518
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004708	short lumbar vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004711	persistence of notochord tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004711	persistence of notochord tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832566
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004848	abnormal liver size		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546167
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005195	abnormal posterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546167
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005270	abnormal zygomatic bone morphology		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005388	respiratory system phenotype		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005458	increased percent body fat/body weight		IEA		N	RGD:5509061	20141003	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005459	decreased percent body fat/body weight		IEA		N	RGD:5509061	20141003	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0005525	increased renal plasma flow rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968670
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20180503	MGI			PMID:26545783
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006399	abnormal long bone epiphyseal ossification zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008069	abnormal joint mobility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008159	increased diameter of fibula		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008161	increased diameter of radius		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008162	increased diameter of tibia		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008163	increased diameter of ulna		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:12814946
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0008736	micromelia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0009882	absent palatal shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0009908	protruding tongue		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8989518
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151008	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8192242
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180503	MGI			PMID:26545783
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276808
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011175	platyspondylia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21538020
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011175	platyspondylia		IAGP		N	RGD:5509061	20180503	MGI			PMID:26545783
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20250508	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011504	abnormal limb long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011504	abnormal limb long bone morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:25541700
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0011812	increased cranium length		IEA		N	RGD:5509061	20171123	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0013817	absent nasal cavity		IAGP		N	RGD:5509061	20171026	MGI			PMID:20730911
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0013945	abnormal elbow joint morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:22028304
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:15132997
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20180503	MGI			PMID:26545783
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0014164	abnormal ciliary process morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:16546167
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0014321	short forelimb		IEA		N	RGD:5509061	20231130	MGI			
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0014430	decreased hyaluronic acid level		IAGP		N	RGD:5509061	20240425	MGI			PMID:16546167
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0030049	prominent forehead		IAGP		N	RGD:5509061	20170921	MGI			PMID:7590256
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0030384	short facial bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:11680679
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0030384	short facial bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:24475193
10373	Col2a1	collagen, type II, alpha 1	gene	MP:0030384	short facial bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:7590256
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808781
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024046
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0003098	decreased tendon stiffness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808781
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808781
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0004507	abnormal ischium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808781
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808781
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006726
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808781
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0030829	abnormal hip joint morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:17588960
10374	Comp	cartilage oligomeric matrix protein	gene	MP:0030829	abnormal hip joint morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:22006726
10378	Comt	catechol-O-methyltransferase	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:9707588
10378	Comt	catechol-O-methyltransferase	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9707588
10378	Comt	catechol-O-methyltransferase	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210128	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20181227	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19930170
10378	Comt	catechol-O-methyltransferase	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9707588
10378	Comt	catechol-O-methyltransferase	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0002294	short gestation period		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20241121	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20160421	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0003106	abnormal fear-related response		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:20618449
10378	Comt	catechol-O-methyltransferase	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160421	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160421	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20190207	MGI			PMID:27388330
10378	Comt	catechol-O-methyltransferase	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:19930170
10378	Comt	catechol-O-methyltransferase	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0009394	increased uterine NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0009455	enhanced cued conditioning behavior		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20151001	MGI			PMID:24509724
10378	Comt	catechol-O-methyltransferase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18469803
10378	Comt	catechol-O-methyltransferase	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20160421	MGI			
10378	Comt	catechol-O-methyltransferase	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20190207	MGI			PMID:27388330
10378	Comt	catechol-O-methyltransferase	gene	MP:0014114	abnormal cognition		IAGP		N	RGD:5509061	20190207	MGI			PMID:27388330
10378	Comt	catechol-O-methyltransferase	gene	MP:0014115	cognitive inflexibility		IAGP		N	RGD:5509061	20190207	MGI			PMID:27388330
10378	Comt	catechol-O-methyltransferase	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
10379	Coq7	demethyl-Q 7	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11716496
10379	Coq7	demethyl-Q 7	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11716496
10379	Coq7	demethyl-Q 7	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11716496
10379	Coq7	demethyl-Q 7	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195414
10379	Coq7	demethyl-Q 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585841
10379	Coq7	demethyl-Q 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11716496
10379	Coq7	demethyl-Q 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847050
10379	Coq7	demethyl-Q 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585841
10379	Coq7	demethyl-Q 7	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11716496
10379	Coq7	demethyl-Q 7	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11716496
10379	Coq7	demethyl-Q 7	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20190926	MGI			PMID:23045551
10379	Coq7	demethyl-Q 7	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847050
10379	Coq7	demethyl-Q 7	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11716496
10379	Coq7	demethyl-Q 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585841
10379	Coq7	demethyl-Q 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11716496
10379	Coq7	demethyl-Q 7	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847050
10379	Coq7	demethyl-Q 7	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847050
10379	Coq7	demethyl-Q 7	gene	MP:0014910	decreased hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:23847050
10380	Cort	cortistatin	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10380	Cort	cortistatin	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10380	Cort	cortistatin	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
10380	Cort	cortistatin	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10380	Cort	cortistatin	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10380	Cort	cortistatin	gene	MP:0005129	increased adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10380	Cort	cortistatin	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10380	Cort	cortistatin	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10380	Cort	cortistatin	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10380	Cort	cortistatin	gene	MP:0011067	abnormal somatostatin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10380	Cort	cortistatin	gene	MP:0011612	increased circulating ghrelin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21971153
10381	Cox6a1	cytochrome c oxidase subunit 6A1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20161103	MGI			PMID:25152455
10381	Cox6a1	cytochrome c oxidase subunit 6A1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20161103	MGI			PMID:25152455
10381	Cox6a1	cytochrome c oxidase subunit 6A1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20161103	MGI			PMID:25152455
10381	Cox6a1	cytochrome c oxidase subunit 6A1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:25152455
10381	Cox6a1	cytochrome c oxidase subunit 6A1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20161103	MGI			PMID:25152455
10381	Cox6a1	cytochrome c oxidase subunit 6A1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:25152455
10381	Cox6a1	cytochrome c oxidase subunit 6A1	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20161103	MGI			PMID:25152455
10382	Cox6a2	cytochrome c oxidase subunit 6A2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788423
10382	Cox6a2	cytochrome c oxidase subunit 6A2	gene	MP:0004011	decreased diastolic filling velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788423
10384	Cp	ceruloplasmin	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393173
10384	Cp	ceruloplasmin	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988052
10384	Cp	ceruloplasmin	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988052
10384	Cp	ceruloplasmin	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036966
10384	Cp	ceruloplasmin	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036966
10384	Cp	ceruloplasmin	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15365174
10384	Cp	ceruloplasmin	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036966
10384	Cp	ceruloplasmin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18804145
10384	Cp	ceruloplasmin	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342521
10384	Cp	ceruloplasmin	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485908
10384	Cp	ceruloplasmin	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342521
10384	Cp	ceruloplasmin	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IEA		N	RGD:5509061	20220519	MGI			
10384	Cp	ceruloplasmin	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18804145
10384	Cp	ceruloplasmin	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988052
10384	Cp	ceruloplasmin	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342521
10384	Cp	ceruloplasmin	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210520	MGI			
10384	Cp	ceruloplasmin	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393173
10384	Cp	ceruloplasmin	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
10384	Cp	ceruloplasmin	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
10384	Cp	ceruloplasmin	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0003043	hypoalgesia		IEA		N	RGD:5509061	20220519	MGI			
10384	Cp	ceruloplasmin	gene	MP:0003065	abnormal liver copper level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11461924
10384	Cp	ceruloplasmin	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18804145
10384	Cp	ceruloplasmin	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393173
10384	Cp	ceruloplasmin	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342521
10384	Cp	ceruloplasmin	gene	MP:0005098	abnormal optic choroid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15365174
10384	Cp	ceruloplasmin	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15365174
10384	Cp	ceruloplasmin	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036966
10384	Cp	ceruloplasmin	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15365174
10384	Cp	ceruloplasmin	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342521
10384	Cp	ceruloplasmin	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342521
10384	Cp	ceruloplasmin	gene	MP:0005549	retina pigment epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15365174
10384	Cp	ceruloplasmin	gene	MP:0005549	retina pigment epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
10384	Cp	ceruloplasmin	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485908
10384	Cp	ceruloplasmin	gene	MP:0005638	hemochromatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17258727
10384	Cp	ceruloplasmin	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210520	MGI			
10384	Cp	ceruloplasmin	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393173
10384	Cp	ceruloplasmin	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15365174
10384	Cp	ceruloplasmin	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342521
10384	Cp	ceruloplasmin	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485908
10384	Cp	ceruloplasmin	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11461924
10384	Cp	ceruloplasmin	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393173
10384	Cp	ceruloplasmin	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485908
10384	Cp	ceruloplasmin	gene	MP:0008811	abnormal brain iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0008811	abnormal brain iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988052
10384	Cp	ceruloplasmin	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15365174
10384	Cp	ceruloplasmin	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12743117
10384	Cp	ceruloplasmin	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
10384	Cp	ceruloplasmin	gene	MP:0011890	increased circulating ferritin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485908
10384	Cp	ceruloplasmin	gene	MP:0011896	increased circulating unsaturated transferrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0012661	decreased circulating ceruloplasmin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485908
10384	Cp	ceruloplasmin	gene	MP:0014175	abnormal ciliary epithelium morphology		IAGP		N	RGD:5509061	20160505	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0014541	increased iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0031696	increased retina iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:12151537
10384	Cp	ceruloplasmin	gene	MP:0031696	increased retina iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:15365174
10384	Cp	ceruloplasmin	gene	MP:0031696	increased retina iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:18326691
10384	Cp	ceruloplasmin	gene	MP:0031696	increased retina iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:22342521
10388	Cpd	carboxypeptidase D	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220519	MGI			
10388	Cpd	carboxypeptidase D	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20220519	MGI			
10388	Cpd	carboxypeptidase D	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20220811	MGI			
10388	Cpd	carboxypeptidase D	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210826	MGI			
10388	Cpd	carboxypeptidase D	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
10388	Cpd	carboxypeptidase D	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
10388	Cpd	carboxypeptidase D	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
10389	Cps1	carbamoyl-phosphate synthetase 1	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20181227	MGI			
10389	Cps1	carbamoyl-phosphate synthetase 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
10389	Cps1	carbamoyl-phosphate synthetase 1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
10389	Cps1	carbamoyl-phosphate synthetase 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
10389	Cps1	carbamoyl-phosphate synthetase 1	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9862865
10389	Cps1	carbamoyl-phosphate synthetase 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20260402	MGI			
10389	Cps1	carbamoyl-phosphate synthetase 1	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
10389	Cps1	carbamoyl-phosphate synthetase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9862865
10389	Cps1	carbamoyl-phosphate synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10390	Cpt1a	carnitine palmitoyltransferase 1a, liver	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16169268
10390	Cpt1a	carnitine palmitoyltransferase 1a, liver	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10390	Cpt1a	carnitine palmitoyltransferase 1a, liver	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
10390	Cpt1a	carnitine palmitoyltransferase 1a, liver	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:25830893
10390	Cpt1a	carnitine palmitoyltransferase 1a, liver	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20160804	MGI			PMID:16169268
10390	Cpt1a	carnitine palmitoyltransferase 1a, liver	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16169268
10390	Cpt1a	carnitine palmitoyltransferase 1a, liver	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16169268
10390	Cpt1a	carnitine palmitoyltransferase 1a, liver	gene	MP:0014508	decreased intestinal crypt stem cell number		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10390	Cpt1a	carnitine palmitoyltransferase 1a, liver	gene	MP:0020316	decreased vascular endothelial cell proliferation		IAGP		N	RGD:5509061	20160616	MGI			PMID:25830893
10391	Cpt1b	carnitine palmitoyltransferase 1b, muscle	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18023382
10391	Cpt1b	carnitine palmitoyltransferase 1b, muscle	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18023382
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20160421	MGI			
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20160421	MGI			
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170504	MGI			
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0002282	abnormal trachea morphology		IEA		N	RGD:5509061	20170504	MGI			
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0005244	hemopericardium		IEA		N	RGD:5509061	20170504	MGI			
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0010439	abnormal hepatic vein morphology		IEA		N	RGD:5509061	20170504	MGI			
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0013852	abnormal Mullerian duct topology		IEA		N	RGD:5509061	20170504	MGI			
10392	Cpt2	carnitine palmitoyltransferase 2	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182786
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344389
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344389
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230119	MGI			
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20251127	MGI			PMID:35181334
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20251127	MGI			PMID:35181334
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20251127	MGI			PMID:35181334
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20251127	MGI			PMID:35181334
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17121542
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279220
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344389
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279220
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20251127	MGI			PMID:35181334
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0014551	impaired neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:17121542
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0014551	impaired neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:17182786
10395	Crmp1	collapsin response mediator protein 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
10396	Dpysl4	dihydropyrimidinase-like 4	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785607
10396	Dpysl4	dihydropyrimidinase-like 4	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785607
10396	Dpysl4	dihydropyrimidinase-like 4	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785607
10396	Dpysl4	dihydropyrimidinase-like 4	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785607
10396	Dpysl4	dihydropyrimidinase-like 4	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785607
10397	Dpysl3	dihydropyrimidinase-like 3	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20201015	MGI			PMID:25225289
10397	Dpysl3	dihydropyrimidinase-like 3	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20201015	MGI			PMID:25225289
10397	Dpysl3	dihydropyrimidinase-like 3	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:22234963
10397	Dpysl3	dihydropyrimidinase-like 3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20201015	MGI			PMID:25225289
10397	Dpysl3	dihydropyrimidinase-like 3	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:22234963
10397	Dpysl3	dihydropyrimidinase-like 3	gene	MP:0009970	increased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20160324	MGI			PMID:22234963
10397	Dpysl3	dihydropyrimidinase-like 3	gene	MP:0012458	decreased hippocampus pyramidal cell length		IAGP		N	RGD:5509061	20160324	MGI			PMID:22234963
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0000203	abnormal circulating aspartate transaminase level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34536564
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:34536564
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34536564
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20231116	MGI			PMID:34536564
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20231116	MGI			PMID:34536564
10398	Crp	C-reactive protein, pentraxin-related	gene	MP:0031060	decreased circulating C-reactive protein level		IAGP		N	RGD:5509061	20200618	MGI			PMID:21149301
10400	Cryab	crystallin, alpha B	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872361
10400	Cryab	crystallin, alpha B	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20240118	MGI			PMID:37435054
10400	Cryab	crystallin, alpha B	gene	MP:0002579	disorganized secondary lens fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872361
10400	Cryab	crystallin, alpha B	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20240118	MGI			PMID:37435054
10400	Cryab	crystallin, alpha B	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872361
10400	Cryab	crystallin, alpha B	gene	MP:0003819	increased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20240118	MGI			PMID:37435054
10400	Cryab	crystallin, alpha B	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:37435054
10400	Cryab	crystallin, alpha B	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20240118	MGI			PMID:37435054
10400	Cryab	crystallin, alpha B	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445271
10400	Cryab	crystallin, alpha B	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20240118	MGI			PMID:37435054
10400	Cryab	crystallin, alpha B	gene	MP:0030938	abnormal reticulophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:23872361
10401	Crybb1	crystallin, beta B1	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20231207	MGI			
10401118	Pgia39_m	proteoglycan induced arthritis 39 (mouse)	qtl	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20151001	MGI			PMID:12794840
10401118	Pgia39_m	proteoglycan induced arthritis 39 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20151001	MGI			PMID:12794840
10401118	Pgia39_m	proteoglycan induced arthritis 39 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:12794840
10401118	Pgia39_m	proteoglycan induced arthritis 39 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:12794840
10401904	Sicd4_m	seizure-induced cell death 4 (mouse)	qtl	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20151015	MGI			PMID:17996456
10401904	Sicd4_m	seizure-induced cell death 4 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20151009	MGI		Created by mouse qtl pipeline	PMID:17996456
10402412	Rmp6_m	resistance to mousepox 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20151023	MGI		Created by mouse qtl pipeline	PMID:1433507
10402412	Rmp6_m	resistance to mousepox 6 (mouse)	qtl	MP:0020929	decreased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:1433507
10402413	Rmp5_m	resistance to mousepox 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20151023	MGI		Created by mouse qtl pipeline	PMID:1433507
10402413	Rmp5_m	resistance to mousepox 5 (mouse)	qtl	MP:0020929	decreased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:1433507
10402414	Sgp5_m	serum gp70 production 5 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20151029	MGI			PMID:15634937
10402414	Sgp5_m	serum gp70 production 5 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20151029	MGI			PMID:15634937
10402414	Sgp5_m	serum gp70 production 5 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20151023	MGI		Created by mouse qtl pipeline	PMID:15634937
10402414	Sgp5_m	serum gp70 production 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20151023	MGI		Created by mouse qtl pipeline	PMID:15634937
10402414	Sgp5_m	serum gp70 production 5 (mouse)	qtl	MP:0005615	increased susceptibility to type III hypersensitivity reaction		IAGP		N	RGD:5509061	20151029	MGI			PMID:15634937
10406	Cryga	crystallin, gamma A	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7088001
10406	Cryga	crystallin, gamma A	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10406	Cryga	crystallin, gamma A	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10406	Cryga	crystallin, gamma A	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10406	Cryga	crystallin, gamma A	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:6510713
10406	Cryga	crystallin, gamma A	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:6877261
10406	Cryga	crystallin, gamma A	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:7088001
10406	Cryga	crystallin, gamma A	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10406	Cryga	crystallin, gamma A	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:7088001
10407	Crygb	crystallin, gamma B	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172107
10407	Crygb	crystallin, gamma B	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:20844585
10407	Crygb	crystallin, gamma B	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172107
10407	Crygb	crystallin, gamma B	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:20844585
10407	Crygb	crystallin, gamma B	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172107
10407	Crygb	crystallin, gamma B	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:6479248
10407	Crygb	crystallin, gamma B	gene	MP:0010262	lamellar cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878859
10408	Crygc	crystallin, gamma C	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
10408	Crygc	crystallin, gamma C	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773036
10408	Crygc	crystallin, gamma C	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10408	Crygc	crystallin, gamma C	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20686773
10408	Crygc	crystallin, gamma C	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20231130	MGI			PMID:37331601
10408	Crygc	crystallin, gamma C	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773036
10408	Crygc	crystallin, gamma C	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10408	Crygc	crystallin, gamma C	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20231130	MGI			PMID:37331601
10408	Crygc	crystallin, gamma C	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:20686773
10408	Crygc	crystallin, gamma C	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210128	MGI			
10408	Crygc	crystallin, gamma C	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20686773
10408	Crygc	crystallin, gamma C	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10408	Crygc	crystallin, gamma C	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20231130	MGI			PMID:37331601
10408	Crygc	crystallin, gamma C	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20686773
10408	Crygc	crystallin, gamma C	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20686773
10408	Crygc	crystallin, gamma C	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:20686773
10408	Crygc	crystallin, gamma C	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20231130	MGI			PMID:37331601
10408	Crygc	crystallin, gamma C	gene	MP:0010255	cortical cataract		IEA		N	RGD:5509061	20190905	MGI			
10408	Crygc	crystallin, gamma C	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
10408	Crygc	crystallin, gamma C	gene	MP:0031345	developmental cataract		IAGP		N	RGD:5509061	20220217	MGI			PMID:20686773
10409	Crygd	crystallin, gamma D	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10409	Crygd	crystallin, gamma D	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704279
10409	Crygd	crystallin, gamma D	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10409	Crygd	crystallin, gamma D	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10409	Crygd	crystallin, gamma D	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652744
10409	Crygd	crystallin, gamma D	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10409	Crygd	crystallin, gamma D	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652744
10409	Crygd	crystallin, gamma D	gene	MP:0006225	ocular rupture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652744
10409	Crygd	crystallin, gamma D	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226711
10409	Crygd	crystallin, gamma D	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652744
10409	Crygd	crystallin, gamma D	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10410	Cryge	crystallin, gamma E	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932192
10410	Cryge	crystallin, gamma E	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511869
10410	Cryge	crystallin, gamma E	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3209064
10410	Cryge	crystallin, gamma E	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20150409	MGI			PMID:1973159
10410	Cryge	crystallin, gamma E	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10410	Cryge	crystallin, gamma E	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3209064
10410	Cryge	crystallin, gamma E	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7011824
10410	Cryge	crystallin, gamma E	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:1973159
10410	Cryge	crystallin, gamma E	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932192
10410	Cryge	crystallin, gamma E	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:12196406
10410	Cryge	crystallin, gamma E	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10410	Cryge	crystallin, gamma E	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511869
10410	Cryge	crystallin, gamma E	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223009
10410	Cryge	crystallin, gamma E	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:3209064
10410	Cryge	crystallin, gamma E	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:7035547
10410	Cryge	crystallin, gamma E	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20150409	MGI			PMID:1973159
10410	Cryge	crystallin, gamma E	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:7215463
10410	Cryge	crystallin, gamma E	gene	MP:0001320	small pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:3209064
10410	Cryge	crystallin, gamma E	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3209064
10410	Cryge	crystallin, gamma E	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12196406
10410	Cryge	crystallin, gamma E	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037589
10410	Cryge	crystallin, gamma E	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7215463
10410	Cryge	crystallin, gamma E	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:1973159
10410	Cryge	crystallin, gamma E	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1811943
10410	Cryge	crystallin, gamma E	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20150409	MGI			PMID:1973159
10410	Cryge	crystallin, gamma E	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20150514	MGI			PMID:7035547
10410	Cryge	crystallin, gamma E	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20150409	MGI			PMID:1973159
10410	Cryge	crystallin, gamma E	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223009
10410	Cryge	crystallin, gamma E	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20150514	MGI			PMID:7035547
10410	Cryge	crystallin, gamma E	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:3209064
10410	Cryge	crystallin, gamma E	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511869
10410	Cryge	crystallin, gamma E	gene	MP:0013731	immature cataract		IAGP		N	RGD:5509061	20150514	MGI			PMID:1973159
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16823860
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000064	failure of bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16823860
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16823860
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16823860
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151022	MGI			PMID:16823860
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0005362	abnormal Langerhans cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16444257
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16823860
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008113	abnormal macrophage differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16444257
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008118	absent Langerhans cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:16444257
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008119	decreased Langerhans cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0010050	hypermyelination		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0010892	increased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20160915	MGI			PMID:25497733
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0010970	abnormal compact bone lamellar structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:11756160
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0030188	round snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:16823860
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0030487	abnormal osteocyte dendritic process morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:15312244
10412	Csf1r	colony stimulating factor 1 receptor	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20180726	MGI			PMID:16823860
10412067	Pain2_m	pain 2 (mouse)	qtl	MP:0001968	abnormal touch/nociception		IAGP		N	RGD:5509061	20151119	MGI			PMID:17686043
10412067	Pain2_m	pain 2 (mouse)	qtl	MP:0003177	allodynia		IAGP		N	RGD:5509061	20151119	MGI			PMID:15979798
10412067	Pain2_m	pain 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	PMID:15979798
10412067	Pain2_m	pain 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	PMID:15979798
10412068	Pbrbc4_m	peripheral blood RBC 4 (mouse)	qtl	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20151119	MGI			PMID:17185011
10412068	Pbrbc4_m	peripheral blood RBC 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	PMID:17185011
10412126	Ril4_m	radiation-induced leukemia sensitivity 4 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	PMID:6300845
10412126	Ril4_m	radiation-induced leukemia sensitivity 4 (mouse)	qtl	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20151119	MGI			PMID:6300845
10412185	Hcs9_m	hepatocarcinogenesis susceptibility 9 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	PMID:15238534
10412185	Hcs9_m	hepatocarcinogenesis susceptibility 9 (mouse)	qtl	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20151119	MGI			PMID:15238534
10412185	Hcs9_m	hepatocarcinogenesis susceptibility 9 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15238534
10412185	Hcs9_m	hepatocarcinogenesis susceptibility 9 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20151119	MGI			PMID:15238534
10412186	Hcs8_m	hepatocarcinogenesis susceptibility 8 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	PMID:15238534
10412186	Hcs8_m	hepatocarcinogenesis susceptibility 8 (mouse)	qtl	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20151119	MGI			PMID:15238534
10412186	Hcs8_m	hepatocarcinogenesis susceptibility 8 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15238534
10412186	Hcs8_m	hepatocarcinogenesis susceptibility 8 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20151119	MGI			PMID:15238534
10412244	Par5_m	pulmonary adenoma resistance 5 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160729	MGI		Created by mouse qtl pipeline	PMID:9331067
10412244	Par5_m	pulmonary adenoma resistance 5 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:9331067
10412244	Par5_m	pulmonary adenoma resistance 5 (mouse)	qtl	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20160728	MGI			PMID:9331067
10414	Csn1s1	casein alpha s1	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:21789179
10414	Csn1s1	casein alpha s1	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20150402	MGI			PMID:21789179
10414	Csn1s1	casein alpha s1	gene	MP:0020880	abnormal milk calcium level		IAGP		N	RGD:5509061	20191226	MGI			PMID:21789179
10414	Csn1s1	casein alpha s1	gene	MP:0020886	abnormal milk phosphate level		IAGP		N	RGD:5509061	20191226	MGI			PMID:21789179
10415	Cst3	cystatin C	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20141016	MGI			PMID:24500719
10415	Cst3	cystatin C	gene	MP:0001102	small superior vagus ganglion		IEA		N	RGD:5509061	20181227	MGI			
10415	Cst3	cystatin C	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748866
10415	Cst3	cystatin C	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141016	MGI			PMID:24500719
10415	Cst3	cystatin C	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141016	MGI			PMID:24500719
10415	Cst3	cystatin C	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:15450354
10415	Cst3	cystatin C	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653570
10415	Cst3	cystatin C	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653570
10415	Cst3	cystatin C	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653570
10415	Cst3	cystatin C	gene	MP:0005489	vascular smooth muscle hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653570
10415	Cst3	cystatin C	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653570
10415	Cst3	cystatin C	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15450354
10415	Cst3	cystatin C	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15450354
10415	Cst3	cystatin C	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24500719
10415	Cst3	cystatin C	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653570
10415	Cst3	cystatin C	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653570
10415	Cst3	cystatin C	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20200102	MGI			PMID:24500719
10417	Cstb	cystatin B	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
10417	Cstb	cystatin B	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934064
10417	Cstb	cystatin B	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934064
10417	Cstb	cystatin B	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20181227	MGI			
10417	Cstb	cystatin B	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934064
10417	Cstb	cystatin B	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0001316	cornea scarring		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934064
10417	Cstb	cystatin B	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934064
10417	Cstb	cystatin B	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
10417	Cstb	cystatin B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20201022	MGI			
10417	Cstb	cystatin B	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934064
10417	Cstb	cystatin B	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20181227	MGI			
10417	Cstb	cystatin B	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
10417	Cstb	cystatin B	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11555622
10417	Cstb	cystatin B	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20201231	MGI			
10417	Cstb	cystatin B	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934064
10417	Cstb	cystatin B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
10417	Cstb	cystatin B	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934064
10417	Cstb	cystatin B	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
10417	Cstb	cystatin B	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20260402	MGI			
10417	Cstb	cystatin B	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0005425	increased macrophage cell number		IEA		N	RGD:5509061	20260402	MGI			
10417	Cstb	cystatin B	gene	MP:0005515	uveitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806543
10417	Cstb	cystatin B	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
10417	Cstb	cystatin B	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20260402	MGI			
10417	Cstb	cystatin B	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20201231	MGI			
10417	Cstb	cystatin B	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
10417	Cstb	cystatin B	gene	MP:0013675	decreased Ly6C-positive mature NK cell number		IEA		N	RGD:5509061	20260402	MGI			
10417	Cstb	cystatin B	gene	MP:0013691	decreased CD5-positive Ly6C-positive T cell number		IEA		N	RGD:5509061	20260402	MGI			
10417	Cstb	cystatin B	gene	MP:0030143	facial muscle spasm		IAGP		N	RGD:5509061	20171005	MGI			PMID:9806543
10421	Ctsc	cathepsin C	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966572
10421	Ctsc	cathepsin C	gene	MP:0001511	disheveled coat		IEA		N	RGD:5509061	20111116	MGI			
10421	Ctsc	cathepsin C	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20111116	MGI			
10421	Ctsc	cathepsin C	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20435891
10421	Ctsc	cathepsin C	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411926
10421	Ctsc	cathepsin C	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292580
10421	Ctsc	cathepsin C	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292580
10421	Ctsc	cathepsin C	gene	MP:0005044	sepsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966572
10421	Ctsc	cathepsin C	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411926
10421	Ctsc	cathepsin C	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411926
10421	Ctsc	cathepsin C	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966572
10421	Ctsc	cathepsin C	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292580
10421	Ctsc	cathepsin C	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292580
10421	Ctsc	cathepsin C	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292580
10421	Ctsc	cathepsin C	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20111116	MGI			
10422	Ctse	cathepsin E	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18000662
10422	Ctse	cathepsin E	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18000662
10422	Ctse	cathepsin E	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18000662
10422	Ctse	cathepsin E	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10422	Ctse	cathepsin E	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769879
10423	Ctsh	cathepsin H	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
10423	Ctsh	cathepsin H	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23830514
10423	Ctsh	cathepsin H	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22022579
10423	Ctsh	cathepsin H	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20435891
10423	Ctsh	cathepsin H	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
10423	Ctsh	cathepsin H	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
10423	Ctsh	cathepsin H	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
10423	Ctsh	cathepsin H	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22022579
10423	Ctsh	cathepsin H	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20240523	MGI			
10423	Ctsh	cathepsin H	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
10424	Ctsl	cathepsin L	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0000376	folliculitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20161216	MGI			PMID:25222295
10424	Ctsl	cathepsin L	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068745
10424	Ctsl	cathepsin L	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782676
10424	Ctsl	cathepsin L	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533435
10424	Ctsl	cathepsin L	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20161216	MGI			PMID:25222295
10424	Ctsl	cathepsin L	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20161216	MGI			PMID:25222295
10424	Ctsl	cathepsin L	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0001282	short vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0001283	sparse vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
10424	Ctsl	cathepsin L	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20161216	MGI			PMID:25222295
10424	Ctsl	cathepsin L	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
10424	Ctsl	cathepsin L	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0002145	abnormal T cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
10424	Ctsl	cathepsin L	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533435
10424	Ctsl	cathepsin L	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0002343	abnormal lymph node cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20180531	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0003865	lymph node inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
10424	Ctsl	cathepsin L	gene	MP:0004085	abnormal heartbeat		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782676
10424	Ctsl	cathepsin L	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
10424	Ctsl	cathepsin L	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533435
10424	Ctsl	cathepsin L	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
10424	Ctsl	cathepsin L	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IEA		N	RGD:5509061	20190418	MGI			
10424	Ctsl	cathepsin L	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20161216	MGI			PMID:25222295
10424	Ctsl	cathepsin L	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0005468	abnormal thyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782676
10424	Ctsl	cathepsin L	gene	MP:0005471	decreased thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782676
10424	Ctsl	cathepsin L	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782676
10424	Ctsl	cathepsin L	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0006045	mitral valve regurgitation		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
10424	Ctsl	cathepsin L	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20161216	MGI			PMID:25222295
10424	Ctsl	cathepsin L	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
10424	Ctsl	cathepsin L	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
10424	Ctsl	cathepsin L	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0008726	increased heart left atrium size		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20161216	MGI			PMID:25222295
10424	Ctsl	cathepsin L	gene	MP:0009600	hypergranulosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0010202	focal dorsal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15154914
10424	Ctsl	cathepsin L	gene	MP:0010505	abnormal T wave		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0010688	hair follicle outer root sheath hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
10424	Ctsl	cathepsin L	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
10424	Ctsl	cathepsin L	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
10424	Ctsl	cathepsin L	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199917
10424	Ctsl	cathepsin L	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
10424	Ctsl	cathepsin L	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5563943
10424	Ctsl	cathepsin L	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20161216	MGI			PMID:25222295
10424	Ctsl	cathepsin L	gene	MP:0011223	dilated lymph node medullary sinus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0011919	abnormal R wave		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20170817	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
10424	Ctsl	cathepsin L	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
10424	Ctsl	cathepsin L	gene	MP:0013251	dental pulp necrosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0013593	enlarged thymus cortex		IAGP		N	RGD:5509061	20150326	MGI			PMID:15905545
10424	Ctsl	cathepsin L	gene	MP:0030515	periodontal ligament necrosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0030571	dilated piliary canal		IAGP		N	RGD:5509061	20180524	MGI			PMID:11023992
10424	Ctsl	cathepsin L	gene	MP:0030571	dilated piliary canal		IAGP		N	RGD:5509061	20180524	MGI			PMID:12163394
10424	Ctsl	cathepsin L	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0031741	decreased T wave amplitude		IAGP		N	RGD:5509061	20260716	MGI			PMID:11972068
10424	Ctsl	cathepsin L	gene	MP:0031743	prolonged T wave		IAGP		N	RGD:5509061	20260716	MGI			PMID:11972068
10425	Cycs	cytochrome c, somatic	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000898	midbrain hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0000919	cranioschisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10830166
10425	Cycs	cytochrome c, somatic	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10830166
10425	Cycs	cytochrome c, somatic	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10830166
10425	Cycs	cytochrome c, somatic	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10830166
10425	Cycs	cytochrome c, somatic	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10830166
10425	Cycs	cytochrome c, somatic	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10830166
10425	Cycs	cytochrome c, somatic	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:15907471
10425	Cycs	cytochrome c, somatic	gene	MP:0030049	prominent forehead		IAGP		N	RGD:5509061	20170921	MGI			PMID:15907471
10426	Cyct	cytochrome c, testis	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101247
10426	Cyct	cytochrome c, testis	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101247
10426	Cyct	cytochrome c, testis	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101247
10426	Cyct	cytochrome c, testis	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101247
10426	Cyct	cytochrome c, testis	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101247
10426	Cyct	cytochrome c, testis	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101247
10426	Cyct	cytochrome c, testis	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101247
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0000635	pituitary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0003353	decreased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0004119	hypokalemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0009078	adrenal gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0009221	uterus adenomyosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0011541	decreased urine aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0011546	increased urine progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0011550	decreased urine corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0011553	increased urine deoxycorticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029289
10428	Cyp11b1	cytochrome P450, family 11, subfamily b, polypeptide 1	gene	MP:0014286	increased adrenal gland zona fasciculata size		IAGP		N	RGD:5509061	20230907	MGI			PMID:19029289
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210204	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0004119	hypokalemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0008291	abnormal adrenocortical cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0008293	abnormal adrenal gland zona glomerulosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0008293	abnormal adrenal gland zona glomerulosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24035414
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731365
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039983
10430	Cyp11b2	cytochrome P450, family 11, subfamily b, polypeptide 2	gene	MP:0031232	increased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:15731365
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17560947
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:17560947
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14980704
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17560947
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17560947
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10623596
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200507	MGI			PMID:31147315
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17560947
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17560947
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19261855
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15094312
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15094312
10436	Cyp1a1	cytochrome P450, family 1, subfamily a, polypeptide 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047483
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14980704
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200507	MGI			PMID:31147315
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0002271	abnormal pulmonary alveolar duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845371
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19261855
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631128
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845371
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9772215
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:15094312
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643688
10438	Cyp1a2	cytochrome P450, family 1, subfamily a, polypeptide 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7761462
10439	Cyp1b1	cytochrome P450, family 1, subfamily b, polypeptide 1	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
10439	Cyp1b1	cytochrome P450, family 1, subfamily b, polypeptide 1	gene	MP:0004223	hypoplastic trabecular meshwork		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
10439	Cyp1b1	cytochrome P450, family 1, subfamily b, polypeptide 1	gene	MP:0004226	absent Schlemm's canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
10439	Cyp1b1	cytochrome P450, family 1, subfamily b, polypeptide 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10051580
10439	Cyp1b1	cytochrome P450, family 1, subfamily b, polypeptide 1	gene	MP:0005203	abnormal trabecular meshwork morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
10439	Cyp1b1	cytochrome P450, family 1, subfamily b, polypeptide 1	gene	MP:0005204	abnormal canal of Schlemm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
10439	Cyp1b1	cytochrome P450, family 1, subfamily b, polypeptide 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910056
10439	Cyp1b1	cytochrome P450, family 1, subfamily b, polypeptide 1	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20150430	MGI			PMID:12624268
10440	Cyp21a1	cytochrome P450, family 21, subfamily a, polypeptide 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20181227	MGI			
10440	Cyp21a1	cytochrome P450, family 21, subfamily a, polypeptide 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
10440	Cyp21a1	cytochrome P450, family 21, subfamily a, polypeptide 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
10440	Cyp21a1	cytochrome P450, family 21, subfamily a, polypeptide 1	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20230601	MGI			
10440	Cyp21a1	cytochrome P450, family 21, subfamily a, polypeptide 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201022	MGI			
10440	Cyp21a1	cytochrome P450, family 21, subfamily a, polypeptide 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
10448274	Actre8_m	activity response to ethanol 8 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20151204	MGI		Created by mouse qtl pipeline	PMID:12882366
10448274	Actre8_m	activity response to ethanol 8 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20151218	MGI		Created by mouse qtl pipeline	PMID:12882366|PMID:11529277
10449382	Pas14_m	pulmonary adenoma susceptibility 14 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160212	MGI		Created by mouse qtl pipeline	PMID:8499946
10449382	Pas14_m	pulmonary adenoma susceptibility 14 (mouse)	qtl	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20160211	MGI			PMID:7813906
10449382	Pas14_m	pulmonary adenoma susceptibility 14 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:8499946
10449382	Pas14_m	pulmonary adenoma susceptibility 14 (mouse)	qtl	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20160211	MGI			PMID:14583591
10449382	Pas14_m	pulmonary adenoma susceptibility 14 (mouse)	qtl	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20160211	MGI			PMID:8666392
10449436	Pas17_m	pulmonary adenoma susceptibility 17 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160101	MGI		Created by mouse qtl pipeline	PMID:8666392
10449436	Pas17_m	pulmonary adenoma susceptibility 17 (mouse)	qtl	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20160107	MGI			PMID:23955086
10449436	Pas17_m	pulmonary adenoma susceptibility 17 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20160101	MGI		Created by mouse qtl pipeline	PMID:8666392
10449436	Pas17_m	pulmonary adenoma susceptibility 17 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20160101	MGI		Created by mouse qtl pipeline	PMID:8666392
10449436	Pas17_m	pulmonary adenoma susceptibility 17 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:8666392
10449436	Pas17_m	pulmonary adenoma susceptibility 17 (mouse)	qtl	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20160107	MGI			PMID:23955086
10449436	Pas17_m	pulmonary adenoma susceptibility 17 (mouse)	qtl	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:8666392
10449437	Pas15_m	pulmonary adenoma susceptibility 15 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160101	MGI		Created by mouse qtl pipeline	PMID:7894154
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17093202
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201231	MGI			
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10772651
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17093202
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17093202
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18990727
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:8662637
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9772215
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:18990727
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18990727
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18990727
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18990727
10451	Cyp2e1	cytochrome P450, family 2, subfamily e, polypeptide 1	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8662637
10452	Cyp2g1	cytochrome P450, family 2, subfamily g, polypeptide 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147558
10452	Cyp2g1	cytochrome P450, family 2, subfamily g, polypeptide 1	gene	MP:0001867	rhinitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147558
10452	Cyp2g1	cytochrome P450, family 2, subfamily g, polypeptide 1	gene	MP:0004512	anosmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147558
10452	Cyp2g1	cytochrome P450, family 2, subfamily g, polypeptide 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:14610229
10452	Cyp2g1	cytochrome P450, family 2, subfamily g, polypeptide 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147558
10452	Cyp2g1	cytochrome P450, family 2, subfamily g, polypeptide 1	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147558
10452	Cyp2g1	cytochrome P450, family 2, subfamily g, polypeptide 1	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147558
10452	Cyp2g1	cytochrome P450, family 2, subfamily g, polypeptide 1	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147558
10457	Cyp4b1	cytochrome P450, family 4, subfamily b, polypeptide 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
10457	Cyp4b1	cytochrome P450, family 4, subfamily b, polypeptide 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20170105	MGI			
10457	Cyp4b1	cytochrome P450, family 4, subfamily b, polypeptide 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10457	Cyp4b1	cytochrome P450, family 4, subfamily b, polypeptide 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
10457	Cyp4b1	cytochrome P450, family 4, subfamily b, polypeptide 1	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20170105	MGI			
10457	Cyp4b1	cytochrome P450, family 4, subfamily b, polypeptide 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748241
10457	Cyp4b1	cytochrome P450, family 4, subfamily b, polypeptide 1	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20260402	MGI			
10457	Cyp4b1	cytochrome P450, family 4, subfamily b, polypeptide 1	gene	MP:0011954	shortened PQ interval		IEA		N	RGD:5509061	20260402	MGI			
10457	Cyp4b1	cytochrome P450, family 4, subfamily b, polypeptide 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001197	oily skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001238	thin epidermis stratum spinosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663430
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11368757
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0002791	steatorrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663430
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0004774	abnormal bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663430
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0005401	abnormal fat-soluble vitamin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0005401	abnormal fat-soluble vitamin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663430
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20201022	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8663429
10458	Cyp7a1	cytochrome P450, family 7, subfamily a, polypeptide 1	gene	MP:0011896	increased circulating unsaturated transferrin level		IEA		N	RGD:5509061	20181227	MGI			
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15710898
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805370
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15710898
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0003378	early sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15710898
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0003572	abnormal uterus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15710898
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0004894	uterus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15710898
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748047
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748048
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15710898
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
10459	Cyp7b1	cytochrome P450, family 7, subfamily b, polypeptide 1	gene	MP:0031020	premature ovarian failure		IAGP		N	RGD:5509061	20200227	MGI			PMID:15710898
10460	Dbh	dopamine beta hydroxylase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001428	adipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001462	abnormal avoidance learning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19864633
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001742	absent circulating adrenaline		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001743	absent circulating noradrenaline		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959968
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15724149
10460	Dbh	dopamine beta hydroxylase	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959968
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959968
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23852112
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959968
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002711	decreased glucagon secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959968
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0002822	catalepsy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20200402	MGI			PMID:32065256
10460	Dbh	dopamine beta hydroxylase	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0003908	decreased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684624
10460	Dbh	dopamine beta hydroxylase	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959968
10460	Dbh	dopamine beta hydroxylase	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959968
10460	Dbh	dopamine beta hydroxylase	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959968
10460	Dbh	dopamine beta hydroxylase	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684624
10460	Dbh	dopamine beta hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19864633
10460	Dbh	dopamine beta hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23852112
10460	Dbh	dopamine beta hydroxylase	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23852112
10460	Dbh	dopamine beta hydroxylase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715704
10460	Dbh	dopamine beta hydroxylase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
10460	Dbh	dopamine beta hydroxylase	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20200402	MGI			PMID:32065256
10460	Dbh	dopamine beta hydroxylase	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
10460	Dbh	dopamine beta hydroxylase	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
10460	Dbh	dopamine beta hydroxylase	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:23684624
10463	Dbi	diazepam binding inhibitor	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316079
10463	Dbi	diazepam binding inhibitor	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316079
10463	Dbi	diazepam binding inhibitor	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316079
10463	Dbi	diazepam binding inhibitor	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316079
10463	Dbi	diazepam binding inhibitor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316079
10463	Dbi	diazepam binding inhibitor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316079
10463	Dbi	diazepam binding inhibitor	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316079
10463	Dbi	diazepam binding inhibitor	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106527
10463	Dbi	diazepam binding inhibitor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559753
10464	Dbp	D site albumin promoter binding protein	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20180705	MGI			PMID:16814730
10464	Dbp	D site albumin promoter binding protein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362490
10464	Dbp	D site albumin promoter binding protein	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20180705	MGI			PMID:20686175
10464	Dbp	D site albumin promoter binding protein	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20180705	MGI			PMID:20686175
10464	Dbp	D site albumin promoter binding protein	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20180705	MGI			PMID:20686175
10464	Dbp	D site albumin promoter binding protein	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20180705	MGI			PMID:16814730
10464	Dbp	D site albumin promoter binding protein	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20180705	MGI			PMID:16814730
10464	Dbp	D site albumin promoter binding protein	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20180705	MGI			PMID:16814730
10464	Dbp	D site albumin promoter binding protein	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0014622	abnormal brain beta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0014624	abnormal brain delta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:15175240
10464	Dbp	D site albumin promoter binding protein	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:9362490
10464	Dbp	D site albumin promoter binding protein	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20171012	MGI			PMID:9362490
10465	Dcc	DCC netrin 1 receptor	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
10465	Dcc	DCC netrin 1 receptor	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22158121
10465	Dcc	DCC netrin 1 receptor	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9331350
10465	Dcc	DCC netrin 1 receptor	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9331350
10465	Dcc	DCC netrin 1 receptor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
10465	Dcc	DCC netrin 1 receptor	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
10465	Dcc	DCC netrin 1 receptor	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126737
10465	Dcc	DCC netrin 1 receptor	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126737
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126737
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22158121
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126737
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22158121
10465	Dcc	DCC netrin 1 receptor	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
10465	Dcc	DCC netrin 1 receptor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9331350
10465	Dcc	DCC netrin 1 receptor	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
10465	Dcc	DCC netrin 1 receptor	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126737
10465	Dcc	DCC netrin 1 receptor	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126737
10465	Dcc	DCC netrin 1 receptor	gene	MP:0009681	abnormal pyramidal decussation morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
10465	Dcc	DCC netrin 1 receptor	gene	MP:0010273	increased classified tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22158121
10465	Dcc	DCC netrin 1 receptor	gene	MP:0010307	abnormal tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
10465	Dcc	DCC netrin 1 receptor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126737
10465	Dcc	DCC netrin 1 receptor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170105	MGI			
10465	Dcc	DCC netrin 1 receptor	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20160317	MGI			PMID:26858598
10465	Dcc	DCC netrin 1 receptor	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:22158121
10465	Dcc	DCC netrin 1 receptor	gene	MP:0014234	decreased enterocyte apoptosis		IAGP		N	RGD:5509061	20230323	MGI			PMID:22158121
10465	Dcc	DCC netrin 1 receptor	gene	MP:0014751	abnormal commissural neuron axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:9126737
10465	Dcc	DCC netrin 1 receptor	gene	MP:0020399	enhanced megakaryocyte emperipolesis		IAGP		N	RGD:5509061	20170803	MGI			PMID:18033315
10465	Dcc	DCC netrin 1 receptor	gene	MP:0020560	abnormal pontine nuclei morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:12451134
10465	Dcc	DCC netrin 1 receptor	gene	MP:0020560	abnormal pontine nuclei morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:9126737
10468	Ace	angiotensin I converting enzyme	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482924
10468	Ace	angiotensin I converting enzyme	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9039095
10468	Ace	angiotensin I converting enzyme	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482924
10468	Ace	angiotensin I converting enzyme	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522949
10468	Ace	angiotensin I converting enzyme	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522949
10468	Ace	angiotensin I converting enzyme	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
10468	Ace	angiotensin I converting enzyme	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075344
10468	Ace	angiotensin I converting enzyme	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221103	MGI			
10468	Ace	angiotensin I converting enzyme	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:9153279
10468	Ace	angiotensin I converting enzyme	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9153279
10468	Ace	angiotensin I converting enzyme	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9153279
10468	Ace	angiotensin I converting enzyme	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331425
10468	Ace	angiotensin I converting enzyme	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075344
10468	Ace	angiotensin I converting enzyme	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20231207	MGI			
10468	Ace	angiotensin I converting enzyme	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9039095
10468	Ace	angiotensin I converting enzyme	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9039095
10468	Ace	angiotensin I converting enzyme	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9039095
10468	Ace	angiotensin I converting enzyme	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687636
10468	Ace	angiotensin I converting enzyme	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687636
10468	Ace	angiotensin I converting enzyme	gene	MP:0002987	abnormal urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9153279
10468	Ace	angiotensin I converting enzyme	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522949
10468	Ace	angiotensin I converting enzyme	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522949
10468	Ace	angiotensin I converting enzyme	gene	MP:0003184	increased angiotensin I-converting enzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651228
10468	Ace	angiotensin I converting enzyme	gene	MP:0003185	decreased angiotensin I-converting enzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0003185	decreased angiotensin I-converting enzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651228
10468	Ace	angiotensin I converting enzyme	gene	MP:0003185	decreased angiotensin I-converting enzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0003185	decreased angiotensin I-converting enzyme activity		IAGP		N	RGD:5509061	20210204	MGI			PMID:14757757
10468	Ace	angiotensin I converting enzyme	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757757
10468	Ace	angiotensin I converting enzyme	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525278
10468	Ace	angiotensin I converting enzyme	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525278
10468	Ace	angiotensin I converting enzyme	gene	MP:0003626	kidney medulla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20221103	MGI			
10468	Ace	angiotensin I converting enzyme	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331425
10468	Ace	angiotensin I converting enzyme	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482924
10468	Ace	angiotensin I converting enzyme	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525278
10468	Ace	angiotensin I converting enzyme	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651228
10468	Ace	angiotensin I converting enzyme	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20200416	MGI			PMID:16001071
10468	Ace	angiotensin I converting enzyme	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9039095
10468	Ace	angiotensin I converting enzyme	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9039095
10468	Ace	angiotensin I converting enzyme	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637363
10468	Ace	angiotensin I converting enzyme	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331425
10468	Ace	angiotensin I converting enzyme	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9153279
10468	Ace	angiotensin I converting enzyme	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522949
10468	Ace	angiotensin I converting enzyme	gene	MP:0006373	abnormal circulating angiotensinogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0006376	decreased circulating angiotensinogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0008543	atrial fibrillation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331425
10468	Ace	angiotensin I converting enzyme	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331425
10468	Ace	angiotensin I converting enzyme	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525278
10468	Ace	angiotensin I converting enzyme	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331425
10468	Ace	angiotensin I converting enzyme	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20191017	MGI			PMID:9482924
10468	Ace	angiotensin I converting enzyme	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651228
10468	Ace	angiotensin I converting enzyme	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482924
10468	Ace	angiotensin I converting enzyme	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210422	MGI			
10468	Ace	angiotensin I converting enzyme	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191017	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0011304	kidney papillary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0011305	dilated kidney calyx		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0011305	dilated kidney calyx		IAGP		N	RGD:5509061	20141003	MGI			PMID:9153279
10468	Ace	angiotensin I converting enzyme	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0011309	abnormal kidney arterial blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0011309	abnormal kidney arterial blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9153279
10468	Ace	angiotensin I converting enzyme	gene	MP:0011317	abnormal renal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0011317	abnormal renal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0011347	abnormal kidney medullary ray morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0011376	abnormal kidney corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0011422	kidney medulla atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0011423	kidney cortex atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753170
10468	Ace	angiotensin I converting enzyme	gene	MP:0011423	kidney cortex atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598926
10468	Ace	angiotensin I converting enzyme	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:9153279
10468	Ace	angiotensin I converting enzyme	gene	MP:0011541	decreased urine aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642790
10468	Ace	angiotensin I converting enzyme	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522949
10468	Ace	angiotensin I converting enzyme	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115616
10468	Ace	angiotensin I converting enzyme	gene	MP:0013254	abnormal angiotensin I-converting enzyme activity		IAGP		N	RGD:5509061	20210204	MGI			PMID:18158355
10468	Ace	angiotensin I converting enzyme	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20191017	MGI			PMID:9482924
10468	Ace	angiotensin I converting enzyme	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220303	MGI			PMID:9482924
10468	Ace	angiotensin I converting enzyme	gene	MP:0031228	decreased angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16001071
10468	Ace	angiotensin I converting enzyme	gene	MP:0031231	decreased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16001071
10468	Ace	angiotensin I converting enzyme	gene	MP:0031231	decreased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:18158355
10469	Ddc	dopa decarboxylase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20200514	MGI			
10469	Ddc	dopa decarboxylase	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0002204	abnormal synaptic neurotransmitter level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0005583	decreased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20240523	MGI			
10469	Ddc	dopa decarboxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10469	Ddc	dopa decarboxylase	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
10469	Ddc	dopa decarboxylase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23275025
10469	Ddc	dopa decarboxylase	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180726	MGI			PMID:28973165
10469	Ddc	dopa decarboxylase	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21701066
10470	Ddx6	DEAD-box helicase 6	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220519	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
10470	Ddx6	DEAD-box helicase 6	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
10470	Ddx6	DEAD-box helicase 6	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20230126	MGI			PMID:36197846
10470	Ddx6	DEAD-box helicase 6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20230126	MGI			PMID:36197846
10470	Ddx6	DEAD-box helicase 6	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
10470	Ddx6	DEAD-box helicase 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220519	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20220811	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20230126	MGI			PMID:36197846
10470	Ddx6	DEAD-box helicase 6	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20230126	MGI			PMID:36197846
10470	Ddx6	DEAD-box helicase 6	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20230126	MGI			PMID:36197846
10470	Ddx6	DEAD-box helicase 6	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
10470	Ddx6	DEAD-box helicase 6	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20230126	MGI			PMID:36197846
10470	Ddx6	DEAD-box helicase 6	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0009361	abnormal primordial ovarian follicle morphology		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
10470	Ddx6	DEAD-box helicase 6	gene	MP:0009850	embryonic lethality between implantation and placentation		IAGP		N	RGD:5509061	20230126	MGI			PMID:36197846
10470	Ddx6	DEAD-box helicase 6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230126	MGI			PMID:36197846
10470	Ddx6	DEAD-box helicase 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
10470	Ddx6	DEAD-box helicase 6	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
10470	Ddx6	DEAD-box helicase 6	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
10470	Ddx6	DEAD-box helicase 6	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
10470	Ddx6	DEAD-box helicase 6	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
10471	Dhfr	dihydrofolate reductase	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20181227	MGI			
10471	Dhfr	dihydrofolate reductase	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210520	MGI			
10471	Dhfr	dihydrofolate reductase	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20180719	MGI			
10471	Dhfr	dihydrofolate reductase	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0011230	abnormal folic acid level		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
10471	Dhfr	dihydrofolate reductase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
10471	Dhfr	dihydrofolate reductase	gene	MP:0013693	abnormal hemopoiesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10471	Dhfr	dihydrofolate reductase	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:26830229
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9516435
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136651
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11309386
10473	Nqo1	NAD(P)H dehydrogenase, quinone 1	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085502
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0002876	abnormal thyroid gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0005468	abnormal thyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0005470	increased thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0005474	increased triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0005477	increased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0005480	increased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10474	Dio1	deiodinase, iodothyronine, type I	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223863
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18842882
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623611
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139088
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105026
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623611
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623611
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18842882
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623611
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0002990	short ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645510
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623611
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003535	absent vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003584	bifid ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003585	large ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003826	abnormal Mullerian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003827	abnormal Wolffian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0003847	disorganized lens bow		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623611
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105026
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105026
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623611
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18842882
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0008794	increased lens epithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623611
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0008796	increased lens fiber apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623611
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0009084	blind uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105026
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0010050	hypermyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:24048858
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238884
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028902
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105026
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011298	ureter hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011365	small metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105026
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011426	abnormal ureter smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011480	impaired ureteric peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172448
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011484	abnormal ureter urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10475	Dlg1	discs large MAGUK scaffold protein 1	gene	MP:0011727	ectopic ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435047
10476	Dlx5	distal-less homeobox 5	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0000041	absent endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0000084	abnormal fontanelle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20171207	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000094	absent alveolar process		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000098	abnormal vomer bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326838
10476	Dlx5	distal-less homeobox 5	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0002238	abnormal nasal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0002249	abnormal larynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0002817	abnormal tooth mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0003163	absent posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0003163	absent posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0003165	absent superior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0003165	absent superior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0003168	abnormal scala vestibuli morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0003800	monodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326838
10476	Dlx5	distal-less homeobox 5	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0003931	absent molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0004237	abnormal pterygoid muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0004311	otic vesicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0004330	abnormal vestibular saccular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0004335	enlarged utricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004409	abnormal crista ampullaris neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0004477	turbinate hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004594	abnormal mandibular coronoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004594	abnormal mandibular coronoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0004665	abnormal stapedial artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326838
10476	Dlx5	distal-less homeobox 5	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0005271	abnormal lacrimal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326838
10476	Dlx5	distal-less homeobox 5	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0006289	otic capsule hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0008023	abnormal styloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0008065	short endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
10476	Dlx5	distal-less homeobox 5	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0008378	small malleus processus brevis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0008379	absent malleus head		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0008380	abnormal gonial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0009893	cleft primary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0009897	decreased maxillary shelf size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0009913	abnormal hyoid bone greater horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0009918	abnormal stylohyoid ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0009942	abnormal olfactory bulb granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0009943	abnormal olfactory bulb periglomerular cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0009954	abnormal mitral cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0010939	abnormal mandibular prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330189
10476	Dlx5	distal-less homeobox 5	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
10476	Dlx5	distal-less homeobox 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20240627	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0013595	absent vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0013597	small vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0014155	absent olfactory epithelium		IAGP		N	RGD:5509061	20160407	MGI			PMID:12533617
10476	Dlx5	distal-less homeobox 5	gene	MP:0014166	ectopic cranial bone		IAGP		N	RGD:5509061	20160407	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0014166	ectopic cranial bone		IAGP		N	RGD:5509061	20160407	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0020350	fused pharyngeal arches		IAGP		N	RGD:5509061	20160915	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0030030	Wormian bones		IAGP		N	RGD:5509061	20170810	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0030055	small lacrimal bone		IAGP		N	RGD:5509061	20170921	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030089	short lower incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030090	short upper incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030148	abnormal mylohyoid muscle morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030187	abnormal epitympanic recess morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030199	deviated nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030203	short nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030208	abnormal intrinsic tongue muscle morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030250	frontonasal prominence hypoplasia		IAGP		N	RGD:5509061	20171026	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030266	small vomer bone		IAGP		N	RGD:5509061	20171026	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030299	lower jaw to upper jaw transformation		IAGP		N	RGD:5509061	20171102	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0030321	abnormal tegmen tympani morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030323	short styloid process		IAGP		N	RGD:5509061	20171109	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:12434331
10476	Dlx5	distal-less homeobox 5	gene	MP:0030422	abnormal outer ear cartilage morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:10433912
10476	Dlx5	distal-less homeobox 5	gene	MP:0030870	abnormal superior horn of thyroid cartilage morphology		IAGP		N	RGD:5509061	20181101	MGI			PMID:10433909
10476	Dlx5	distal-less homeobox 5	gene	MP:0030870	abnormal superior horn of thyroid cartilage morphology		IAGP		N	RGD:5509061	20181101	MGI			PMID:10433912
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20241121	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626497
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20180215	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20200723	MGI			PMID:30854433
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9299538
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20170525	MGI			PMID:26365037
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371627
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22734004
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9681470
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20160714	MGI			PMID:26966179
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20170525	MGI			PMID:26365037
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20170706	MGI			PMID:25530839
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20180712	MGI			PMID:29187645
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20200723	MGI			PMID:30854433
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20210311	MGI			PMID:28505980
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10204788
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385524
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3239377
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719885
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1686056
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:26365037
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371627
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371627
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540561
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540561
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385524
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24200690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8099842
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694376
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8099842
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19401296
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2144875
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8433102
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626497
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694130
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19401296
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626497
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626497
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694376
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694130
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1635838
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1865908
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9299538
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1865908
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20260101	MGI			PMID:39099311
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002899	fatigue		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20210520	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002952	ventricular cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20180215	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2407807
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2919177
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2967442
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3209690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3239377
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20160714	MGI			PMID:26966179
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24200690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2919177
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2919177
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20170713	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003358	abnormal hypaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20260101	MGI			PMID:39099311
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210520	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694130
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3239377
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:29187645
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19401296
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003950	abnormal plasma membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11432672
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004036	abnormal muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857961
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004089	dilated sarcoplasmic reticulum		IAGP		N	RGD:5509061	20141003	MGI			PMID:3239377
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004089	dilated sarcoplasmic reticulum		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22734004
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24200690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004142	abnormal muscle tone		IAGP		N	RGD:5509061	20141003	MGI			PMID:3209690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2250175
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857961
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004246	abnormal extensor digitorum longus morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004248	abnormal epaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371627
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20160929	MGI			PMID:17889902
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20170525	MGI			PMID:26365037
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20180712	MGI			PMID:29187645
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20200723	MGI			PMID:30854433
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20210311	MGI			PMID:28505980
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:2919177
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004597	increased susceptibility to noise-induced hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12148865
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:8186696
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005137	increased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8064326
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810924
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:24200690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24200690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20210520	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040037
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10068512
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7843915
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24200690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385524
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2967442
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288752
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0006190	retina ischemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812982
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008327	abnormal corticotroph morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8064326
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008416	increased somatotroph cell size		IAGP		N	RGD:5509061	20150129	MGI			PMID:8064326
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008837	increased transforming growth factor beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008838	decreased transforming growth factor beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:8047301
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009398	abnormal skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009398	abnormal skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694130
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694376
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694130
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371627
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:3209690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:8186696
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371627
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385524
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8099842
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20180712	MGI			PMID:29187645
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20201224	MGI			PMID:32483152
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:1635838
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385524
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:22734004
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810924
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:2967442
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:8186696
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288751
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20160714	MGI			PMID:26966179
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20180215	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20180712	MGI			PMID:29187645
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20200723	MGI			PMID:30854433
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009405	increased skeletal muscle fiber number		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:3239377
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694376
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371627
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:2919177
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20200723	MGI			PMID:30854433
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694376
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2967442
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3239377
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8186696
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20160714	MGI			PMID:26966179
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20170525	MGI			PMID:26365037
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21931825
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009416	cardiac muscle degeneration		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1635838
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20160714	MGI			PMID:26966179
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20200716	MGI			PMID:26365037
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20200723	MGI			PMID:30854433
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:32483152
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20210311	MGI			PMID:28505980
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8186696
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:17889902
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8186696
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371627
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20170525	MGI			PMID:26365037
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20180712	MGI			PMID:29187645
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200723	MGI			PMID:30854433
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20260101	MGI			PMID:39099311
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210826	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810924
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2967442
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8064326
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20160714	MGI			PMID:26966179
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20170525	MGI			PMID:26365037
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20200402	MGI			PMID:31028078
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20200723	MGI			PMID:30854433
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010106	abnormal circulating pyruvate kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6583703
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010106	abnormal circulating pyruvate kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9681470
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010226	increased quadriceps weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010238	increased skeletal muscle weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010238	increased skeletal muscle weight		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371627
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:20304955
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010252	anterior subcapsular cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:2250175
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:2250175
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857961
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010509	decreased P wave amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857961
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010581	abnormal atrium myocardial trabeculae morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8099842
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20141003	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:24200690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20260101	MGI			PMID:32988972
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20260101	MGI			PMID:39099311
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12148865
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20160714	MGI			PMID:26966179
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0012735	abnormal response to exercise		IAGP		N	RGD:5509061	20260101	MGI			PMID:39099311
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0013237	abnormal skeletal muscle regeneration		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211104	MGI			PMID:32483152
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:22076929
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0013467	diaphragmitis		IAGP		N	RGD:5509061	20160929	MGI			PMID:17889902
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:21893021
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20250313	MGI			PMID:38602028
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0014740	increased auditory brainstem response wave peak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:12148865
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0014742	increased auditory brainstem response wave interpeak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:12148865
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0015068	decreased myocardial fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0020280	increased creatine kinase level		IAGP		N	RGD:5509061	20180712	MGI			PMID:29187645
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0020309	increased creatine kinase activity		IAGP		N	RGD:5509061	20151217	MGI			PMID:26566673
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0020309	increased creatine kinase activity		IAGP		N	RGD:5509061	20170706	MGI			PMID:25530839
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0020330	increased capillary density		IAGP		N	RGD:5509061	20160714	MGI			PMID:20705734
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0020879	abnormal calcium level		IAGP		N	RGD:5509061	20210311	MGI			PMID:28505980
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0020938	decreased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:24200690
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0030428	abnormal scalene muscle morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:1865908
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:21145579
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:23831727
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0030957	abnormal myotube morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:19535499
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:19401296
10479	Dmd	dystrophin, muscular dystrophy	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:21931825
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200625	MGI			PMID:31339932
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:27795435
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20200625	MGI			PMID:31339932
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20200709	MGI			PMID:26124093
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20200402	MGI			PMID:27892925
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10823914
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200402	MGI			PMID:26124093
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200402	MGI			PMID:27892925
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200402	MGI			PMID:28348219
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200702	MGI			PMID:27795435
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20200402	MGI			PMID:26124093
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200402	MGI			PMID:27892925
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10823914
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10823914
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10823914
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20200402	MGI			PMID:28348219
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20200402	MGI			PMID:28348219
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20200702	MGI			PMID:27795435
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200625	MGI			PMID:31339932
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10823914
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:27795435
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:27795435
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:27795435
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20200402	MGI			PMID:27892925
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0010858	pulmonary epithelial necrosis		IAGP		N	RGD:5509061	20200702	MGI			PMID:27795435
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0010894	pulmonary alveolar edema		IAGP		N	RGD:5509061	20200402	MGI			PMID:27892925
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0011018	pulmonary hyaline membrane formation		IAGP		N	RGD:5509061	20200402	MGI			PMID:28348219
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0012041	increased susceptibility to pulmonary hyaline membrane formation		IAGP		N	RGD:5509061	20200402	MGI			PMID:27892925
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:26124093
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:27892925
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28348219
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200625	MGI			PMID:31339932
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200702	MGI			PMID:27795435
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0031047	decreased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:27892925
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:27892925
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:28348219
10481	Dpp4	dipeptidylpeptidase 4	gene	MP:0031053	pleuritis		IAGP		N	RGD:5509061	20200702	MGI			PMID:27795435
10482	Prl8a2	prolactin family 8, subfamily a, member 2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166917
10482	Prl8a2	prolactin family 8, subfamily a, member 2	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166917
10482	Prl8a2	prolactin family 8, subfamily a, member 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166917
10482	Prl8a2	prolactin family 8, subfamily a, member 2	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166917
10482	Prl8a2	prolactin family 8, subfamily a, member 2	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166917
10482	Prl8a2	prolactin family 8, subfamily a, member 2	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166917
10482	Prl8a2	prolactin family 8, subfamily a, member 2	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166917
10485	Drd1	dopamine receptor D1	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7954836
10485	Drd1	dopamine receptor D1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7809078
10485	Drd1	dopamine receptor D1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7954836
10485	Drd1	dopamine receptor D1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10585522
10485	Drd1	dopamine receptor D1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884517
10485	Drd1	dopamine receptor D1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172752
10485	Drd1	dopamine receptor D1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615733
10485	Drd1	dopamine receptor D1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7954836
10485	Drd1	dopamine receptor D1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23569242
10485	Drd1	dopamine receptor D1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7954836
10485	Drd1	dopamine receptor D1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001143
10485	Drd1	dopamine receptor D1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884517
10485	Drd1	dopamine receptor D1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884517
10485	Drd1	dopamine receptor D1	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20220421	MGI			PMID:8001143
10485	Drd1	dopamine receptor D1	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10585522
10485	Drd1	dopamine receptor D1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884517
10485	Drd1	dopamine receptor D1	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172752
10485	Drd1	dopamine receptor D1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18644244
10485	Drd1	dopamine receptor D1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:7809078
10485	Drd1	dopamine receptor D1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:7809078
10485	Drd1	dopamine receptor D1	gene	MP:0001512	trunk curl		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615733
10485	Drd1	dopamine receptor D1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615733
10485	Drd1	dopamine receptor D1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884517
10485	Drd1	dopamine receptor D1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7809078
10485	Drd1	dopamine receptor D1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7809078
10485	Drd1	dopamine receptor D1	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764243
10485	Drd1	dopamine receptor D1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10485	Drd1	dopamine receptor D1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10485	Drd1	dopamine receptor D1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884517
10485	Drd1	dopamine receptor D1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884517
10485	Drd1	dopamine receptor D1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7809078
10485	Drd1	dopamine receptor D1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884517
10485	Drd1	dopamine receptor D1	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172752
10485	Drd1	dopamine receptor D1	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22356538
10485	Drd1	dopamine receptor D1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22356538
10485	Drd1	dopamine receptor D1	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0003246	loss of GABAergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409246
10485	Drd1	dopamine receptor D1	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0003460	decreased fear-related response		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10485	Drd1	dopamine receptor D1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001143
10485	Drd1	dopamine receptor D1	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074012
10485	Drd1	dopamine receptor D1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615733
10485	Drd1	dopamine receptor D1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764243
10485	Drd1	dopamine receptor D1	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409246
10485	Drd1	dopamine receptor D1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18486343
10485	Drd1	dopamine receptor D1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001143
10485	Drd1	dopamine receptor D1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10485	Drd1	dopamine receptor D1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20151217	MGI			PMID:24496082
10485	Drd1	dopamine receptor D1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014726
10485	Drd1	dopamine receptor D1	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18045908
10485	Drd1	dopamine receptor D1	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:7954836
10485	Drd1	dopamine receptor D1	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014726
10485	Drd1	dopamine receptor D1	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:18045908
10485	Drd1	dopamine receptor D1	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001143
10485	Drd1	dopamine receptor D1	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18486343
10485	Drd1	dopamine receptor D1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615733
10485	Drd1	dopamine receptor D1	gene	MP:0010167	decreased response to stress-induced hyperthermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18486343
10485	Drd1	dopamine receptor D1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10485	Drd1	dopamine receptor D1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7954836
10485	Drd1	dopamine receptor D1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10485	Drd1	dopamine receptor D1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:7954836
10485	Drd1	dopamine receptor D1	gene	MP:0012559	decreased forebrain volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:9822743
10485	Drd1	dopamine receptor D1	gene	MP:0014620	abnormal interictal brain wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0020083	decreased hippocampus volume		IAGP		N	RGD:5509061	20170706	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0020340	abnormal inhibitory learning		IAGP		N	RGD:5509061	20160915	MGI			PMID:10585522
10485	Drd1	dopamine receptor D1	gene	MP:0030986	striatum atrophy		IAGP		N	RGD:5509061	20191128	MGI			PMID:17360497
10485	Drd1	dopamine receptor D1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:17360497
10486	Drd2	dopamine receptor D2	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0000635	pituitary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0000636	enlarged pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0000636	enlarged pituitary gland		IAGP		N	RGD:5509061	20150129	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0000646	enlarged adrenocortical cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158626
10486	Drd2	dopamine receptor D2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391470
10486	Drd2	dopamine receptor D2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10956362
10486	Drd2	dopamine receptor D2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525059
10486	Drd2	dopamine receptor D2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391470
10486	Drd2	dopamine receptor D2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069937
10486	Drd2	dopamine receptor D2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196569
10486	Drd2	dopamine receptor D2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391470
10486	Drd2	dopamine receptor D2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9547254
10486	Drd2	dopamine receptor D2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196569
10486	Drd2	dopamine receptor D2	gene	MP:0001396	unidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534241
10486	Drd2	dopamine receptor D2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
10486	Drd2	dopamine receptor D2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196569
10486	Drd2	dopamine receptor D2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069937
10486	Drd2	dopamine receptor D2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11864730
10486	Drd2	dopamine receptor D2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19840852
10486	Drd2	dopamine receptor D2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9547254
10486	Drd2	dopamine receptor D2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18644244
10486	Drd2	dopamine receptor D2	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391470
10486	Drd2	dopamine receptor D2	gene	MP:0001506	limp posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382674
10486	Drd2	dopamine receptor D2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525059
10486	Drd2	dopamine receptor D2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0001744	hypersecretion of corticosterone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158626
10486	Drd2	dopamine receptor D2	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391470
10486	Drd2	dopamine receptor D2	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391470
10486	Drd2	dopamine receptor D2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
10486	Drd2	dopamine receptor D2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158626
10486	Drd2	dopamine receptor D2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0002570	alcohol aversion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196569
10486	Drd2	dopamine receptor D2	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11864730
10486	Drd2	dopamine receptor D2	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0002676	uterus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069937
10486	Drd2	dopamine receptor D2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11864730
10486	Drd2	dopamine receptor D2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9547254
10486	Drd2	dopamine receptor D2	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15061865
10486	Drd2	dopamine receptor D2	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
10486	Drd2	dopamine receptor D2	gene	MP:0002822	catalepsy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069974
10486	Drd2	dopamine receptor D2	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158626
10486	Drd2	dopamine receptor D2	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
10486	Drd2	dopamine receptor D2	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:10341260
10486	Drd2	dopamine receptor D2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409246
10486	Drd2	dopamine receptor D2	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534241
10486	Drd2	dopamine receptor D2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16280580
10486	Drd2	dopamine receptor D2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9547254
10486	Drd2	dopamine receptor D2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23242137
10486	Drd2	dopamine receptor D2	gene	MP:0003371	decreased circulating estrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0003462	abnormal response to novel odor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765459
10486	Drd2	dopamine receptor D2	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684868
10486	Drd2	dopamine receptor D2	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
10486	Drd2	dopamine receptor D2	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9140068
10486	Drd2	dopamine receptor D2	gene	MP:0003546	decreased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196569
10486	Drd2	dopamine receptor D2	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11303741
10486	Drd2	dopamine receptor D2	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11864730
10486	Drd2	dopamine receptor D2	gene	MP:0003867	increased defecation amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525059
10486	Drd2	dopamine receptor D2	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0003973	increased pituitary hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9140068
10486	Drd2	dopamine receptor D2	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069974
10486	Drd2	dopamine receptor D2	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11864730
10486	Drd2	dopamine receptor D2	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0005117	increased circulating pituitary hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0005137	increased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391470
10486	Drd2	dopamine receptor D2	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069937
10486	Drd2	dopamine receptor D2	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:9140068
10486	Drd2	dopamine receptor D2	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9140068
10486	Drd2	dopamine receptor D2	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0005573	increased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10956362
10486	Drd2	dopamine receptor D2	gene	MP:0005575	increased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10956362
10486	Drd2	dopamine receptor D2	gene	MP:0005576	decreased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10956362
10486	Drd2	dopamine receptor D2	gene	MP:0005585	increased tidal volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:10956362
10486	Drd2	dopamine receptor D2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19840852
10486	Drd2	dopamine receptor D2	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0005646	abnormal pituitary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0006001	abnormal intestinal transit time		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525059
10486	Drd2	dopamine receptor D2	gene	MP:0006003	abnormal large intestinal transit time		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525059
10486	Drd2	dopamine receptor D2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409246
10486	Drd2	dopamine receptor D2	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0006299	abnormal latent inhibition of conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15061865
10486	Drd2	dopamine receptor D2	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069974
10486	Drd2	dopamine receptor D2	gene	MP:0008294	abnormal adrenal gland zona fasciculata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0008295	abnormal adrenal gland zona reticularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0008299	adrenal cortical hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0008324	abnormal melanotroph morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0008329	decreased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0008329	decreased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0008331	increased lactotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0008331	increased lactotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0008335	decreased gonadotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0008337	increased thyrotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0008370	enlarged pituitary intermediate lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:9140068
10486	Drd2	dopamine receptor D2	gene	MP:0008371	pituitary intermediate lobe hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0008371	pituitary intermediate lobe hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9717839
10486	Drd2	dopamine receptor D2	gene	MP:0008423	decreased lactotroph cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23242137
10486	Drd2	dopamine receptor D2	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566895
10486	Drd2	dopamine receptor D2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
10486	Drd2	dopamine receptor D2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9547254
10486	Drd2	dopamine receptor D2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18486343
10486	Drd2	dopamine receptor D2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
10486	Drd2	dopamine receptor D2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9547254
10486	Drd2	dopamine receptor D2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
10486	Drd2	dopamine receptor D2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23242137
10486	Drd2	dopamine receptor D2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23242137
10486	Drd2	dopamine receptor D2	gene	MP:0008939	increased pituitary gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0009016	abnormal estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0009089	short uterine horn		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0009221	uterus adenomyosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9252189
10486	Drd2	dopamine receptor D2	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069937
10486	Drd2	dopamine receptor D2	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12650980
10486	Drd2	dopamine receptor D2	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089973
10486	Drd2	dopamine receptor D2	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069937
10486	Drd2	dopamine receptor D2	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089973
10486	Drd2	dopamine receptor D2	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10341260
10486	Drd2	dopamine receptor D2	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
10486	Drd2	dopamine receptor D2	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196569
10486	Drd2	dopamine receptor D2	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18486343
10486	Drd2	dopamine receptor D2	gene	MP:0009778	impaired behavioral response to anesthetic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0009779	enhanced behavioral response to anesthetic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745501
10486	Drd2	dopamine receptor D2	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
10486	Drd2	dopamine receptor D2	gene	MP:0010167	decreased response to stress-induced hyperthermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18486343
10486	Drd2	dopamine receptor D2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15272078
10486	Drd2	dopamine receptor D2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391470
10486	Drd2	dopamine receptor D2	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534241
10486	Drd2	dopamine receptor D2	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23242137
10486	Drd2	dopamine receptor D2	gene	MP:0011532	decreased urine major urinary protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23536095
10486	Drd2	dopamine receptor D2	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897683
10486	Drd2	dopamine receptor D2	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525059
10486	Drd2	dopamine receptor D2	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525059
10486	Drd2	dopamine receptor D2	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566118
10486	Drd2	dopamine receptor D2	gene	MP:0013334	adenohypophysis peliosis		IAGP		N	RGD:5509061	20141204	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0013348	adenohypophysis hyperplasia		IAGP		N	RGD:5509061	20150129	MGI			PMID:9247267
10486	Drd2	dopamine receptor D2	gene	MP:0013348	adenohypophysis hyperplasia		IAGP		N	RGD:5509061	20150129	MGI			PMID:9247268
10486	Drd2	dopamine receptor D2	gene	MP:0013355	adenohypophysis hypertrophy		IAGP		N	RGD:5509061	20150129	MGI			PMID:9247267
10487	Drd4	dopamine receptor D4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9323127
10487	Drd4	dopamine receptor D4	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531457
10487	Drd4	dopamine receptor D4	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9323127
10487	Drd4	dopamine receptor D4	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764243
10487	Drd4	dopamine receptor D4	gene	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9323127
10487	Drd4	dopamine receptor D4	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9323127
10487	Drd4	dopamine receptor D4	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684868
10487	Drd4	dopamine receptor D4	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9323127
10487	Drd4	dopamine receptor D4	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764243
10487	Drd4	dopamine receptor D4	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9323127
10487	Drd4	dopamine receptor D4	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:9323127
10489	Drd5	dopamine receptor D5	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486173
10489	Drd5	dopamine receptor D5	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15598876
10489	Drd5	dopamine receptor D5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10489	Drd5	dopamine receptor D5	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10489	Drd5	dopamine receptor D5	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486173
10489	Drd5	dopamine receptor D5	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486173
10489	Drd5	dopamine receptor D5	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15598876
10489	Drd5	dopamine receptor D5	gene	MP:0002909	abnormal adrenal gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486173
10489	Drd5	dopamine receptor D5	gene	MP:0003460	decreased fear-related response		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10489	Drd5	dopamine receptor D5	gene	MP:0004183	abnormal sympathetic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486173
10489	Drd5	dopamine receptor D5	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486173
10489	Drd5	dopamine receptor D5	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15598876
10489	Drd5	dopamine receptor D5	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486173
10489	Drd5	dopamine receptor D5	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15598876
10489	Drd5	dopamine receptor D5	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10489	Drd5	dopamine receptor D5	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141120	MGI			PMID:24843151
10489	Drd5	dopamine receptor D5	gene	MP:0031303	enhanced behavioral response to methamphetamine		IAGP		N	RGD:5509061	20211028	MGI			PMID:24155877
10493	Dspp	dentin sialophosphoprotein	gene	MP:0000126	brittle teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12721295
10493	Dspp	dentin sialophosphoprotein	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20190207	MGI			PMID:16937369
10493	Dspp	dentin sialophosphoprotein	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20190207	MGI			PMID:16937369
10493	Dspp	dentin sialophosphoprotein	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12721295
10493	Dspp	dentin sialophosphoprotein	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20170105	MGI			
10493	Dspp	dentin sialophosphoprotein	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12721295
10493	Dspp	dentin sialophosphoprotein	gene	MP:0002819	abnormal dental pulp cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12721295
10493	Dspp	dentin sialophosphoprotein	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0003933	abnormal cementum morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
10493	Dspp	dentin sialophosphoprotein	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20170105	MGI			
10493	Dspp	dentin sialophosphoprotein	gene	MP:0011035	abnormal branching involved in alveolar duct morphogenesis		IAGP		N	RGD:5509061	20190207	MGI			PMID:16937369
10493	Dspp	dentin sialophosphoprotein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
10493	Dspp	dentin sialophosphoprotein	gene	MP:0011365	small metanephros		IAGP		N	RGD:5509061	20190207	MGI			PMID:16937369
10493	Dspp	dentin sialophosphoprotein	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20190207	MGI			PMID:16937369
10493	Dspp	dentin sialophosphoprotein	gene	MP:0011457	abnormal metanephric ureteric bud development		IAGP		N	RGD:5509061	20190207	MGI			PMID:16937369
10493	Dspp	dentin sialophosphoprotein	gene	MP:0012024	abnormal nephron morphogenesis		IAGP		N	RGD:5509061	20190207	MGI			PMID:16937369
10493	Dspp	dentin sialophosphoprotein	gene	MP:0012026	abnormal S-shaped body morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:16937369
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030131	abnormal periodontium morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030132	periodontium inflammation		IAGP		N	RGD:5509061	20171026	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030451	abnormal dentin mineralization		IAGP		N	RGD:5509061	20171221	MGI			PMID:12721295
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030466	alveolar process atrophy		IAGP		N	RGD:5509061	20171221	MGI			PMID:12721295
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030466	alveolar process atrophy		IAGP		N	RGD:5509061	20171221	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030484	abnormal osteocyte lacuna morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030486	abnormal osteocyte canaliculus morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030490	periodontal pocket		IAGP		N	RGD:5509061	20180111	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030516	abnormal junctional epithelium morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030517	detached junctional epithelium		IAGP		N	RGD:5509061	20180111	MGI			PMID:22934831
10493	Dspp	dentin sialophosphoprotein	gene	MP:0030543	abnormal predentin morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:12721295
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16137572
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20150910	MGI			PMID:26008897
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22293606
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22293606
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22293606
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22293606
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20151022	MGI			PMID:26374847
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0002892	decreased superior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20150910	MGI			PMID:26008897
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20151022	MGI			PMID:26374847
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20150910	MGI			PMID:26008897
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20150910	MGI			PMID:26008897
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0006105	small tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20150910	MGI			PMID:26008897
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20150910	MGI			PMID:26008897
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20150910	MGI			PMID:26008897
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20150910	MGI			PMID:26008897
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20151022	MGI			PMID:26374847
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16137572
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20151022	MGI			PMID:26374847
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0012088	abnormal midbrain size		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0012263	decreased hindbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192061
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0014115	cognitive inflexibility		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0020083	decreased hippocampus volume		IAGP		N	RGD:5509061	20170706	MGI			PMID:22293606
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0020568	abnormal premotor cortex morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:16137572
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20220512	MGI			PMID:29223763
10495	Dyrk1a	dual-specificity tyrosine phosphorylation regulated kinase 1a	gene	MP:0031660	prenatal lethality prior to heart atrial septation, incomplete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10499	Edn1	endothelin 1	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0000114	cleft chin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314687
10499	Edn1	endothelin 1	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516397
10499	Edn1	endothelin 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20200227	MGI			PMID:20516397
10499	Edn1	endothelin 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632412
10499	Edn1	endothelin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516397
10499	Edn1	endothelin 1	gene	MP:0002318	hypercapnia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10626068
10499	Edn1	endothelin 1	gene	MP:0002329	abnormal blood gas level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10626068
10499	Edn1	endothelin 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632412
10499	Edn1	endothelin 1	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0004181	abnormal carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0004183	abnormal sympathetic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10626068
10499	Edn1	endothelin 1	gene	MP:0004205	absent hyoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314687
10499	Edn1	endothelin 1	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193100
10499	Edn1	endothelin 1	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764893
10499	Edn1	endothelin 1	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10626068
10499	Edn1	endothelin 1	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516397
10499	Edn1	endothelin 1	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10626068
10499	Edn1	endothelin 1	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0005611	decreased circulating antidiuretic hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632412
10499	Edn1	endothelin 1	gene	MP:0005634	decreased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632412
10499	Edn1	endothelin 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868309
10499	Edn1	endothelin 1	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516397
10499	Edn1	endothelin 1	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516397
10499	Edn1	endothelin 1	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314687
10499	Edn1	endothelin 1	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0006344	small second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632412
10499	Edn1	endothelin 1	gene	MP:0009524	absent submandibular gland		IAGP		N	RGD:5509061	20150101	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632412
10499	Edn1	endothelin 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0010486	absent right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0010543	aorta tubular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0010544	interrupted aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7615798
10499	Edn1	endothelin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20516397
10499	Edn1	endothelin 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8152482
10499	Edn1	endothelin 1	gene	MP:0030427	abnormal neck muscle morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:8152482
10505	Ednrb	endothelin receptor type B	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:6049665
10505	Ednrb	endothelin receptor type B	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:6049665
10505	Ednrb	endothelin receptor type B	gene	MP:0000163	abnormal cartilage morphology		IEA		N	RGD:5509061	20111116	MGI			
10505	Ednrb	endothelin receptor type B	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0000373	belly spot		IEA		N	RGD:5509061	20141003	MGI			
10505	Ednrb	endothelin receptor type B	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20190110	MGI			PMID:27134165
10505	Ednrb	endothelin receptor type B	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945437
10505	Ednrb	endothelin receptor type B	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945437
10505	Ednrb	endothelin receptor type B	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:5917257
10505	Ednrb	endothelin receptor type B	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591209
10505	Ednrb	endothelin receptor type B	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20150618	MGI			PMID:5917257
10505	Ednrb	endothelin receptor type B	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729956
10505	Ednrb	endothelin receptor type B	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729956
10505	Ednrb	endothelin receptor type B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693272
10505	Ednrb	endothelin receptor type B	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048069
10505	Ednrb	endothelin receptor type B	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:13943454
10505	Ednrb	endothelin receptor type B	gene	MP:0001574	abnormal oxygen level		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729956
10505	Ednrb	endothelin receptor type B	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5917257
10505	Ednrb	endothelin receptor type B	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20150618	MGI			PMID:8041763
10505	Ednrb	endothelin receptor type B	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20190110	MGI			PMID:27134165
10505	Ednrb	endothelin receptor type B	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
10505	Ednrb	endothelin receptor type B	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:5917257
10505	Ednrb	endothelin receptor type B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591209
10505	Ednrb	endothelin receptor type B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812796
10505	Ednrb	endothelin receptor type B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693272
10505	Ednrb	endothelin receptor type B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150618	MGI			PMID:5917257
10505	Ednrb	endothelin receptor type B	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
10505	Ednrb	endothelin receptor type B	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
10505	Ednrb	endothelin receptor type B	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729956
10505	Ednrb	endothelin receptor type B	gene	MP:0002318	hypercapnia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10626068
10505	Ednrb	endothelin receptor type B	gene	MP:0002329	abnormal blood gas level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10626068
10505	Ednrb	endothelin receptor type B	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:6049665
10505	Ednrb	endothelin receptor type B	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591209
10505	Ednrb	endothelin receptor type B	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812796
10505	Ednrb	endothelin receptor type B	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:13800713
10505	Ednrb	endothelin receptor type B	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:2304907
10505	Ednrb	endothelin receptor type B	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:5917257
10505	Ednrb	endothelin receptor type B	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371807
10505	Ednrb	endothelin receptor type B	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24043815
10505	Ednrb	endothelin receptor type B	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868309
10505	Ednrb	endothelin receptor type B	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693272
10505	Ednrb	endothelin receptor type B	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12644183
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801484
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17246828
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693272
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:2304907
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713933
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:8138159
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371807
10505	Ednrb	endothelin receptor type B	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0002939	head spot		IEA		N	RGD:5509061	20141003	MGI			
10505	Ednrb	endothelin receptor type B	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17246828
10505	Ednrb	endothelin receptor type B	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17246842
10505	Ednrb	endothelin receptor type B	gene	MP:0003027	abnormal blood pH regulation		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0003032	hypocapnia		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10496965
10505	Ednrb	endothelin receptor type B	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812796
10505	Ednrb	endothelin receptor type B	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713933
10505	Ednrb	endothelin receptor type B	gene	MP:0003154	abnormal soft palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801484
10505	Ednrb	endothelin receptor type B	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:6049665
10505	Ednrb	endothelin receptor type B	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868309
10505	Ednrb	endothelin receptor type B	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
10505	Ednrb	endothelin receptor type B	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801484
10505	Ednrb	endothelin receptor type B	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0004302	abnormal Deiters cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:6049665
10505	Ednrb	endothelin receptor type B	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0004364	thin stria vascularis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20190110	MGI			PMID:27134165
10505	Ednrb	endothelin receptor type B	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945437
10505	Ednrb	endothelin receptor type B	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10626068
10505	Ednrb	endothelin receptor type B	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10626068
10505	Ednrb	endothelin receptor type B	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10496965
10505	Ednrb	endothelin receptor type B	gene	MP:0005100	abnormal choroid pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591209
10505	Ednrb	endothelin receptor type B	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812796
10505	Ednrb	endothelin receptor type B	gene	MP:0005174	abnormal tail pigmentation		IEA		N	RGD:5509061	20111116	MGI			
10505	Ednrb	endothelin receptor type B	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
10505	Ednrb	endothelin receptor type B	gene	MP:0005508	abnormal skeleton morphology		IEA		N	RGD:5509061	20111116	MGI			
10505	Ednrb	endothelin receptor type B	gene	MP:0005583	decreased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868309
10505	Ednrb	endothelin receptor type B	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801484
10505	Ednrb	endothelin receptor type B	gene	MP:0005600	increased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0006010	absent strial intermediate cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773966
10505	Ednrb	endothelin receptor type B	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868309
10505	Ednrb	endothelin receptor type B	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868309
10505	Ednrb	endothelin receptor type B	gene	MP:0006274	abnormal urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868309
10505	Ednrb	endothelin receptor type B	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693272
10505	Ednrb	endothelin receptor type B	gene	MP:0008569	lethality at weaning		IEA		N	RGD:5509061	20141225	MGI			
10505	Ednrb	endothelin receptor type B	gene	MP:0008732	reduced hair shaft melanin granule number		IAGP		N	RGD:5509061	20190110	MGI			PMID:27134165
10505	Ednrb	endothelin receptor type B	gene	MP:0008786	abnormal hindgut morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:4772386
10505	Ednrb	endothelin receptor type B	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0009379	abnormal foot pigmentation		IEA		N	RGD:5509061	20111116	MGI			
10505	Ednrb	endothelin receptor type B	gene	MP:0009388	abnormal epidermal melanocyte morphology		IAGP		N	RGD:5509061	20190110	MGI			PMID:27134165
10505	Ednrb	endothelin receptor type B	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801484
10505	Ednrb	endothelin receptor type B	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868309
10505	Ednrb	endothelin receptor type B	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0009891	abnormal palate bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
10505	Ednrb	endothelin receptor type B	gene	MP:0010016	variable depigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001159
10505	Ednrb	endothelin receptor type B	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945437
10505	Ednrb	endothelin receptor type B	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048069
10505	Ednrb	endothelin receptor type B	gene	MP:0010741	abnormal melanocyte proliferation		IAGP		N	RGD:5509061	20150618	MGI			PMID:8041763
10505	Ednrb	endothelin receptor type B	gene	MP:0010741	abnormal melanocyte proliferation		IAGP		N	RGD:5509061	20190110	MGI			PMID:27134165
10505	Ednrb	endothelin receptor type B	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801484
10505	Ednrb	endothelin receptor type B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8138159
10505	Ednrb	endothelin receptor type B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371807
10505	Ednrb	endothelin receptor type B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2304907
10505	Ednrb	endothelin receptor type B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8138159
10505	Ednrb	endothelin receptor type B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371807
10505	Ednrb	endothelin receptor type B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8138159
10505	Ednrb	endothelin receptor type B	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1352884
10505	Ednrb	endothelin receptor type B	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8138159
10505	Ednrb	endothelin receptor type B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
10505	Ednrb	endothelin receptor type B	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2304907
10505	Ednrb	endothelin receptor type B	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8138159
10505	Ednrb	endothelin receptor type B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150618	MGI			PMID:5917257
10505	Ednrb	endothelin receptor type B	gene	MP:0011494	abnormal pigmentation pattern		IAGP		N	RGD:5509061	20150618	MGI			PMID:5917257
10505	Ednrb	endothelin receptor type B	gene	MP:0011494	abnormal pigmentation pattern		IAGP		N	RGD:5509061	20150618	MGI			PMID:8041763
10505	Ednrb	endothelin receptor type B	gene	MP:0012023	decreased melanocyte number		IAGP		N	RGD:5509061	20190110	MGI			PMID:27134165
10505	Ednrb	endothelin receptor type B	gene	MP:0013006	abnormal enteric neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693272
10505	Ednrb	endothelin receptor type B	gene	MP:0013404	decreased circulating lactate level		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240367
10505	Ednrb	endothelin receptor type B	gene	MP:0013701	abnormal mature B cell number		IAGP		N	RGD:5509061	20170525	MGI			PMID:26061883
10505	Ednrb	endothelin receptor type B	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:24945437
10505	Ednrb	endothelin receptor type B	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:20048069
10505	Ednrb	endothelin receptor type B	gene	MP:0014484	decreased feces water content		IAGP		N	RGD:5509061	20240704	MGI			PMID:24945437
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20200924	MGI			PMID:30838762
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20160428	MGI			PMID:25755286
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472894
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20160428	MGI			PMID:25670349
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0009083	uterus hypertrophy		IAGP		N	RGD:5509061	20220407	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0011120	increased primordial ovarian follicle number		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0011124	increased primary ovarian follicle number		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20150129	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0013475	delayed reproductive senescence		IAGP		N	RGD:5509061	20220616	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0031383	increased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:24582807
10506	Eef2k	eukaryotic elongation factor-2 kinase	gene	MP:0031421	increased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:24582807
10508	Efnb1	ephrin B1	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19515977
10508	Efnb1	ephrin B1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968134
10508	Efnb1	ephrin B1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19515977
10508	Efnb1	ephrin B1	gene	MP:0000155	asymmetric rib joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19515977
10508	Efnb1	ephrin B1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0000618	small salivary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
10508	Efnb1	ephrin B1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19515977
10508	Efnb1	ephrin B1	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968134
10508	Efnb1	ephrin B1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19515977
10508	Efnb1	ephrin B1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
10508	Efnb1	ephrin B1	gene	MP:0003840	abnormal coronal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968134
10508	Efnb1	ephrin B1	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968134
10508	Efnb1	ephrin B1	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19515977
10508	Efnb1	ephrin B1	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21847105
10508	Efnb1	ephrin B1	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
10508	Efnb1	ephrin B1	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0009882	absent palatal shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19515977
10508	Efnb1	ephrin B1	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
10508	Efnb1	ephrin B1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919674
10508	Efnb1	ephrin B1	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15037550
10508	Efnb1	ephrin B1	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:21976681
10509	Efnb3	ephrin B3	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12649481
10509	Efnb3	ephrin B3	gene	MP:0001393	ataxia		IEA		N	RGD:5509061	20150910	MGI			
10509	Efnb3	ephrin B3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182083
10509	Efnb3	ephrin B3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182083
10509	Efnb3	ephrin B3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297511
10509	Efnb3	ephrin B3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12649481
10509	Efnb3	ephrin B3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182796
10509	Efnb3	ephrin B3	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14699416
10509	Efnb3	ephrin B3	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20150910	MGI			
10509	Efnb3	ephrin B3	gene	MP:0001524	impaired limb coordination		IEA		N	RGD:5509061	20141003	MGI			
10509	Efnb3	ephrin B3	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:14699416
10509	Efnb3	ephrin B3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182083
10509	Efnb3	ephrin B3	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182083
10509	Efnb3	ephrin B3	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
10509	Efnb3	ephrin B3	gene	MP:0002862	abnormal righting response		IEA		N	RGD:5509061	20141003	MGI			
10509	Efnb3	ephrin B3	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182083
10509	Efnb3	ephrin B3	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297511
10509	Efnb3	ephrin B3	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12649481
10509	Efnb3	ephrin B3	gene	MP:0003880	abnormal central pattern generator function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12649481
10509	Efnb3	ephrin B3	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182796
10509	Efnb3	ephrin B3	gene	MP:0008960	abnormal axon pruning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182796
10509	Efnb3	ephrin B3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20150910	MGI			
10510	Egf	epidermal growth factor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456865
10510	Egf	epidermal growth factor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
10510	Egf	epidermal growth factor	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
10510	Egf	epidermal growth factor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456865
10510	Egf	epidermal growth factor	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0002580	duodenal lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
10510	Egf	epidermal growth factor	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
10510	Egf	epidermal growth factor	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
10510	Egf	epidermal growth factor	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
10510	Egf	epidermal growth factor	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
10510	Egf	epidermal growth factor	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20150402	MGI			PMID:10331984
10511	Egfr	epidermal growth factor receptor	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319864
10511	Egfr	epidermal growth factor receptor	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319864
10511	Egfr	epidermal growth factor receptor	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
10511	Egfr	epidermal growth factor receptor	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
10511	Egfr	epidermal growth factor receptor	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830272
10511	Egfr	epidermal growth factor receptor	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000384	distorted hair follicle pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000396	increased curvature of hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:5142632
10511	Egfr	epidermal growth factor receptor	gene	MP:0000399	increased curvature of guard hairs		IEA		N	RGD:5509061	20111116	MGI			
10511	Egfr	epidermal growth factor receptor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
10511	Egfr	epidermal growth factor receptor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
10511	Egfr	epidermal growth factor receptor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:19115345
10511	Egfr	epidermal growth factor receptor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:5142632
10511	Egfr	epidermal growth factor receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0000446	long snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0000448	pointed snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319864
10511	Egfr	epidermal growth factor receptor	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
10511	Egfr	epidermal growth factor receptor	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
10511	Egfr	epidermal growth factor receptor	gene	MP:0000583	long toenails		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
10511	Egfr	epidermal growth factor receptor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7533293
10511	Egfr	epidermal growth factor receptor	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000763	abnormal filiform papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830272
10511	Egfr	epidermal growth factor receptor	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830272
10511	Egfr	epidermal growth factor receptor	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
10511	Egfr	epidermal growth factor receptor	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20170309	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20160616	MGI			
10511	Egfr	epidermal growth factor receptor	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
10511	Egfr	epidermal growth factor receptor	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
10511	Egfr	epidermal growth factor receptor	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
10511	Egfr	epidermal growth factor receptor	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
10511	Egfr	epidermal growth factor receptor	gene	MP:0001221	epidermal atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041656
10511	Egfr	epidermal growth factor receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
10511	Egfr	epidermal growth factor receptor	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001279	wavy vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0001280	loss of vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0001282	short vibrissae		IEA		N	RGD:5509061	20111116	MGI			
10511	Egfr	epidermal growth factor receptor	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
10511	Egfr	epidermal growth factor receptor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20141003	MGI			
10511	Egfr	epidermal growth factor receptor	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20160310	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0001316	cornea scarring		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
10511	Egfr	epidermal growth factor receptor	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0001511	disheveled coat		IEA		N	RGD:5509061	20160616	MGI			
10511	Egfr	epidermal growth factor receptor	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19115345
10511	Egfr	epidermal growth factor receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19115345
10511	Egfr	epidermal growth factor receptor	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19115345
10511	Egfr	epidermal growth factor receptor	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7533293
10511	Egfr	epidermal growth factor receptor	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821760
10511	Egfr	epidermal growth factor receptor	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21119595
10511	Egfr	epidermal growth factor receptor	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
10511	Egfr	epidermal growth factor receptor	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
10511	Egfr	epidermal growth factor receptor	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
10511	Egfr	epidermal growth factor receptor	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
10511	Egfr	epidermal growth factor receptor	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125255
10511	Egfr	epidermal growth factor receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
10511	Egfr	epidermal growth factor receptor	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
10511	Egfr	epidermal growth factor receptor	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
10511	Egfr	epidermal growth factor receptor	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
10511	Egfr	epidermal growth factor receptor	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
10511	Egfr	epidermal growth factor receptor	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125255
10511	Egfr	epidermal growth factor receptor	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456865
10511	Egfr	epidermal growth factor receptor	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0002268	abnormal terminal bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
10511	Egfr	epidermal growth factor receptor	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20250410	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
10511	Egfr	epidermal growth factor receptor	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21119595
10511	Egfr	epidermal growth factor receptor	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21119595
10511	Egfr	epidermal growth factor receptor	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:5142632
10511	Egfr	epidermal growth factor receptor	gene	MP:0003819	increased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0003820	increased left ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20170309	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821760
10511	Egfr	epidermal growth factor receptor	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19115345
10511	Egfr	epidermal growth factor receptor	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0005099	abnormal ciliary body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821760
10511	Egfr	epidermal growth factor receptor	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821760
10511	Egfr	epidermal growth factor receptor	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20160310	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0006026	dilated terminal bronchiole tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0006116	calcified aortic valve		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0006257	abnormal fungiform papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0006265	increased pulse pressure		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
10511	Egfr	epidermal growth factor receptor	gene	MP:0008090	increased T-helper 2 cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
10511	Egfr	epidermal growth factor receptor	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17940036
10511	Egfr	epidermal growth factor receptor	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17940036
10511	Egfr	epidermal growth factor receptor	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
10511	Egfr	epidermal growth factor receptor	gene	MP:0008816	petechiae		IAGP		N	RGD:5509061	20170309	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20170309	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0008862	asymmetric snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0008899	plush coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821760
10511	Egfr	epidermal growth factor receptor	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20141225	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17940036
10511	Egfr	epidermal growth factor receptor	gene	MP:0009801	abnormal hair cortex keratinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:5142632
10511	Egfr	epidermal growth factor receptor	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20170309	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0010179	rough coat		IEA		N	RGD:5509061	20160616	MGI			
10511	Egfr	epidermal growth factor receptor	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
10511	Egfr	epidermal growth factor receptor	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21119595
10511	Egfr	epidermal growth factor receptor	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0010506	prolonged RR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0010570	prolonged ST segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20240125	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0010856	dilated respiratory conducting tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0010897	abnormal bronchiole epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0010900	abnormal pulmonary interalveolar septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0010911	abnormal pulmonary acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9205141
10511	Egfr	epidermal growth factor receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
10511	Egfr	epidermal growth factor receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411909
10511	Egfr	epidermal growth factor receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0011092	embryonic lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
10511	Egfr	epidermal growth factor receptor	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
10511	Egfr	epidermal growth factor receptor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7630400
10511	Egfr	epidermal growth factor receptor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020428
10511	Egfr	epidermal growth factor receptor	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0011926	abnormal heart valve physiology		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20170810	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20160310	MGI			PMID:9030684
10511	Egfr	epidermal growth factor receptor	gene	MP:0012099	decreased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0012099	decreased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618084
10511	Egfr	epidermal growth factor receptor	gene	MP:0012099	decreased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7618085
10511	Egfr	epidermal growth factor receptor	gene	MP:0013542	abnormal submandibular gland branching morphogenesis		IAGP		N	RGD:5509061	20150326	MGI			PMID:10521784
10511	Egfr	epidermal growth factor receptor	gene	MP:0014107	premature chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:12925580
10511	Egfr	epidermal growth factor receptor	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28404843
10511	Egfr	epidermal growth factor receptor	gene	MP:0030026	small Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:10319864
10511	Egfr	epidermal growth factor receptor	gene	MP:0030191	narrow snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:15366372
10511	Egfr	epidermal growth factor receptor	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:28404843
10511	Egfr	epidermal growth factor receptor	gene	MP:0031324	delayed liver regeneration		IAGP		N	RGD:5509061	20220106	MGI			PMID:17940036
10511	Egfr	epidermal growth factor receptor	gene	MP:0031580	enlarged semilunar valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:10700187
10511	Egfr	epidermal growth factor receptor	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:25997932
10511	Egfr	epidermal growth factor receptor	gene	MP:0031634	decreased heart right ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:25997932
10512	Egr1	early growth response 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792003
10512	Egr1	early growth response 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792003
10512	Egr1	early growth response 1	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15940638
10512	Egr1	early growth response 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916644
10512	Egr1	early growth response 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679873
10512	Egr1	early growth response 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
10512	Egr1	early growth response 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001573	abnormal circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15940638
10512	Egr1	early growth response 1	gene	MP:0001573	abnormal circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916644
10512	Egr1	early growth response 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170105	MGI			
10512	Egr1	early growth response 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001746	abnormal pituitary secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15940638
10512	Egr1	early growth response 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916644
10512	Egr1	early growth response 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289506
10512	Egr1	early growth response 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679873
10512	Egr1	early growth response 1	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739581
10512	Egr1	early growth response 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0001928	abnormal ovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15958557
10512	Egr1	early growth response 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135623
10512	Egr1	early growth response 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135623
10512	Egr1	early growth response 1	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:17197510
10512	Egr1	early growth response 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17197510
10512	Egr1	early growth response 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289506
10512	Egr1	early growth response 1	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0002697	abnormal eye size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17197510
10512	Egr1	early growth response 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20170105	MGI			
10512	Egr1	early growth response 1	gene	MP:0002774	small prostate gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0002801	abnormal long-term object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:14622575
10512	Egr1	early growth response 1	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679873
10512	Egr1	early growth response 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10710348
10512	Egr1	early growth response 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20170105	MGI			
10512	Egr1	early growth response 1	gene	MP:0003426	pulmonary interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679873
10512	Egr1	early growth response 1	gene	MP:0003642	absent seminal vesicle		IEA		N	RGD:5509061	20170105	MGI			
10512	Egr1	early growth response 1	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18208539
10512	Egr1	early growth response 1	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20170105	MGI			
10512	Egr1	early growth response 1	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20170105	MGI			
10512	Egr1	early growth response 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
10512	Egr1	early growth response 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265859
10512	Egr1	early growth response 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265859
10512	Egr1	early growth response 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18397757
10512	Egr1	early growth response 1	gene	MP:0004848	abnormal liver size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15940638
10512	Egr1	early growth response 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10710348
10512	Egr1	early growth response 1	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819371
10512	Egr1	early growth response 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18208539
10512	Egr1	early growth response 1	gene	MP:0005184	abnormal circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0005340	abnormal susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14670837
10512	Egr1	early growth response 1	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265859
10512	Egr1	early growth response 1	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135623
10512	Egr1	early growth response 1	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289506
10512	Egr1	early growth response 1	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679873
10512	Egr1	early growth response 1	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18208539
10512	Egr1	early growth response 1	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20170105	MGI			
10512	Egr1	early growth response 1	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20201231	MGI			
10512	Egr1	early growth response 1	gene	MP:0008329	decreased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0008365	adenohypophysis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0008552	abnormal circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916644
10512	Egr1	early growth response 1	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15940638
10512	Egr1	early growth response 1	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:9440815
10512	Egr1	early growth response 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15940638
10512	Egr1	early growth response 1	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20161027	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15940638
10512	Egr1	early growth response 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135623
10512	Egr1	early growth response 1	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:15958557
10512	Egr1	early growth response 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20170105	MGI			
10512	Egr1	early growth response 1	gene	MP:0012432	decreased prostate gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135623
10512	Egr1	early growth response 1	gene	MP:0013599	Leydig cell atrophy		IAGP		N	RGD:5509061	20150319	MGI			PMID:8703054
10512	Egr1	early growth response 1	gene	MP:0014655	abnormal cornea curvature		IAGP		N	RGD:5509061	20250508	MGI			PMID:17197510
10512	Egr1	early growth response 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:17420284
10512	Egr1	early growth response 1	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:17197510
10516	Cela1	chymotrypsin-like elastase family, member 1	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:29420065
10516	Cela1	chymotrypsin-like elastase family, member 1	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:29420065
10516	Cela1	chymotrypsin-like elastase family, member 1	gene	MP:0011044	increased lung elastance		IAGP		N	RGD:5509061	20190926	MGI			PMID:29420065
10516	Cela1	chymotrypsin-like elastase family, member 1	gene	MP:0011163	increased wet-to-dry lung weight ratio		IAGP		N	RGD:5509061	20190926	MGI			PMID:29420065
10518	Elk1	ETS transcription factor ELK1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673163
10518	Elk1	ETS transcription factor ELK1	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20210128	MGI			
10518	Elk1	ETS transcription factor ELK1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14994271
10518	Elk1	ETS transcription factor ELK1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
10519	Emd	emerin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507906
10519	Emd	emerin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:25274778
10519	Emd	emerin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507906
10519	Emd	emerin	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20171116	MGI			PMID:25274778
10519	Emd	emerin	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20230601	MGI			
10519	Emd	emerin	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
10519	Emd	emerin	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20171116	MGI			PMID:25274778
10519	Emd	emerin	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16403804
10519	Emd	emerin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507906
10519	Emd	emerin	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507906
10519	Emd	emerin	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20171116	MGI			PMID:25274778
10519	Emd	emerin	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20171116	MGI			PMID:25274778
10519	Emd	emerin	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20171116	MGI			PMID:25274778
10519	Emd	emerin	gene	MP:0006321	increased myocardial fiber number		IAGP		N	RGD:5509061	20171116	MGI			PMID:25274778
10519	Emd	emerin	gene	MP:0009455	enhanced cued conditioning behavior		IEA		N	RGD:5509061	20230601	MGI			
10519	Emd	emerin	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20171116	MGI			PMID:25274778
10519	Emd	emerin	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:25274778
10519	Emd	emerin	gene	MP:0031634	decreased heart right ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:25274778
10520	Emp1	epithelial membrane protein 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
10521	Eno1	enolase 1, alpha non-neuron	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626503
10521	Eno1	enolase 1, alpha non-neuron	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626503
10521	Eno1	enolase 1, alpha non-neuron	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626503
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758458
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758458
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0001003	abnormal olfactory receptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989651
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19132103
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19132103
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0001460	abnormal olfactory discrimination memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989651
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758458
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989651
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19132103
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989651
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19132103
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19132103
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0004082	abnormal habenula morphology		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989651
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758458
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0008462	abnormal medium spiny neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19132103
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758458
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758458
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20151217	MGI			PMID:24496082
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0009756	impaired behavioral response to nicotine		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20250508	MGI			
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20141030	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:23487260
10527	Eno2	enolase 2, gamma neuronal	gene	MP:0021012	decreased acetylcholine level		IAGP		N	RGD:5509061	20260709	MGI			PMID:23487260
10528	Eno3	enolase 3, beta muscle	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20230601	MGI			
10528	Eno3	enolase 3, beta muscle	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20230601	MGI			
10529	Ephx1	epoxide hydrolase 1, microsomal	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10446164
10530	Stx2	syntaxin 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18277055
10530	Stx2	syntaxin 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18277055
10530	Stx2	syntaxin 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
10530	Stx2	syntaxin 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
10530	Stx2	syntaxin 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18277055
10530	Stx2	syntaxin 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
10530	Stx2	syntaxin 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
10530	Stx2	syntaxin 2	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0004910	decreased seminal vesicle weight		IEA		N	RGD:5509061	20111116	MGI			
10530	Stx2	syntaxin 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18277055
10530	Stx2	syntaxin 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
10530	Stx2	syntaxin 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
10530	Stx2	syntaxin 2	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
10530	Stx2	syntaxin 2	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18277055
10530	Stx2	syntaxin 2	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20160526	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20160526	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0013955	increased colon length		IAGP		N	RGD:5509061	20160304	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0013957	increased small intestine length		IAGP		N	RGD:5509061	20160526	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20160526	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0014081	branched small intestinal villi		IAGP		N	RGD:5509061	20160526	MGI			PMID:16710473
10530	Stx2	syntaxin 2	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:18277055
10531	Epo	erythropoietin	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20959632
10531	Epo	erythropoietin	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20959632
10531	Epo	erythropoietin	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10531	Epo	erythropoietin	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10531	Epo	erythropoietin	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12239150
10531	Epo	erythropoietin	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878311
10531	Epo	erythropoietin	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10531	Epo	erythropoietin	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8264149
10531	Epo	erythropoietin	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10531	Epo	erythropoietin	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0002319	hyperoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878311
10531	Epo	erythropoietin	gene	MP:0002320	hyperventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878311
10531	Epo	erythropoietin	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12239150
10531	Epo	erythropoietin	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20959632
10531	Epo	erythropoietin	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20959632
10531	Epo	erythropoietin	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10531	Epo	erythropoietin	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10531	Epo	erythropoietin	gene	MP:0003913	increased heart right ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878311
10531	Epo	erythropoietin	gene	MP:0003913	increased heart right ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330260
10531	Epo	erythropoietin	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878311
10531	Epo	erythropoietin	gene	MP:0004032	abnormal interventricular groove morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12239150
10531	Epo	erythropoietin	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12239150
10531	Epo	erythropoietin	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12239150
10531	Epo	erythropoietin	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878311
10531	Epo	erythropoietin	gene	MP:0005575	increased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878311
10531	Epo	erythropoietin	gene	MP:0005575	increased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330260
10531	Epo	erythropoietin	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15531367
10531	Epo	erythropoietin	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12239150
10531	Epo	erythropoietin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20959632
10531	Epo	erythropoietin	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10531	Epo	erythropoietin	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10531	Epo	erythropoietin	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:7553874
10531	Epo	erythropoietin	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:7553874
10531	Epo	erythropoietin	gene	MP:0031589	detached epicardium		IAGP		N	RGD:5509061	20240229	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406592
10532	Epor	erythropoietin receptor	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
10532	Epor	erythropoietin receptor	gene	MP:0000216	absent erythroid progenitor cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941827
10532	Epor	erythropoietin receptor	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
10532	Epor	erythropoietin receptor	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
10532	Epor	erythropoietin receptor	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16534010
10532	Epor	erythropoietin receptor	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
10532	Epor	erythropoietin receptor	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10532	Epor	erythropoietin receptor	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8566749
10532	Epor	erythropoietin receptor	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
10532	Epor	erythropoietin receptor	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10532	Epor	erythropoietin receptor	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8566749
10532	Epor	erythropoietin receptor	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
10532	Epor	erythropoietin receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
10532	Epor	erythropoietin receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10532	Epor	erythropoietin receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8566749
10532	Epor	erythropoietin receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
10532	Epor	erythropoietin receptor	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10532	Epor	erythropoietin receptor	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
10532	Epor	erythropoietin receptor	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8566749
10532	Epor	erythropoietin receptor	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406592
10532	Epor	erythropoietin receptor	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
10532	Epor	erythropoietin receptor	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
10532	Epor	erythropoietin receptor	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
10532	Epor	erythropoietin receptor	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
10532	Epor	erythropoietin receptor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
10532	Epor	erythropoietin receptor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
10532	Epor	erythropoietin receptor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8566749
10532	Epor	erythropoietin receptor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
10532	Epor	erythropoietin receptor	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10532	Epor	erythropoietin receptor	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
10532	Epor	erythropoietin receptor	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16534010
10532	Epor	erythropoietin receptor	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16534010
10532	Epor	erythropoietin receptor	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606578
10532	Epor	erythropoietin receptor	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20200820	MGI			PMID:32093902
10532	Epor	erythropoietin receptor	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10532	Epor	erythropoietin receptor	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16534010
10532	Epor	erythropoietin receptor	gene	MP:0004032	abnormal interventricular groove morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0004230	abnormal embryonic erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8566749
10532	Epor	erythropoietin receptor	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436614
10532	Epor	erythropoietin receptor	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
10532	Epor	erythropoietin receptor	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:16534010
10532	Epor	erythropoietin receptor	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20180503	MGI			PMID:28169986
10532	Epor	erythropoietin receptor	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180503	MGI			PMID:28169986
10532	Epor	erythropoietin receptor	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15531367
10532	Epor	erythropoietin receptor	gene	MP:0008105	increased amacrine cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32093902
10532	Epor	erythropoietin receptor	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32093902
10532	Epor	erythropoietin receptor	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32093902
10532	Epor	erythropoietin receptor	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20200820	MGI			PMID:32093902
10532	Epor	erythropoietin receptor	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20200820	MGI			PMID:32093902
10532	Epor	erythropoietin receptor	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20180503	MGI			PMID:28169986
10532	Epor	erythropoietin receptor	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
10532	Epor	erythropoietin receptor	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
10532	Epor	erythropoietin receptor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16534010
10532	Epor	erythropoietin receptor	gene	MP:0010755	abnormal heart right ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16534010
10532	Epor	erythropoietin receptor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8566749
10532	Epor	erythropoietin receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15090451
10532	Epor	erythropoietin receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8799165
10532	Epor	erythropoietin receptor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409505
10532	Epor	erythropoietin receptor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7553874
10532	Epor	erythropoietin receptor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158582
10532	Epor	erythropoietin receptor	gene	MP:0011243	decreased fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
10532	Epor	erythropoietin receptor	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
10532	Epor	erythropoietin receptor	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20200820	MGI			PMID:32093902
10532	Epor	erythropoietin receptor	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200820	MGI			PMID:32093902
10532	Epor	erythropoietin receptor	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200820	MGI			PMID:32093902
10532	Epor	erythropoietin receptor	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:11406592
10532	Epor	erythropoietin receptor	gene	MP:0015008	abnormal fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:11406592
10532	Epor	erythropoietin receptor	gene	MP:0015014	enhanced bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:11406592
10532	Epor	erythropoietin receptor	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:7553874
10532	Epor	erythropoietin receptor	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:8566749
10532	Epor	erythropoietin receptor	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20210805	MGI			PMID:18854306
10532	Epor	erythropoietin receptor	gene	MP:0031589	detached epicardium		IAGP		N	RGD:5509061	20240229	MGI			PMID:10409505
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809799
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000293	absent myocardial trabeculae		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000293	absent myocardial trabeculae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000296	absent trabeculae carneae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000296	absent trabeculae carneae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809799
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000296	absent trabeculae carneae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637684
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12526770
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716706
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044753
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792428
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19954518
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564761
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496447
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000992	absent primary muscle spindle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000995	absent secondary muscle spindle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0000996	partial loss of secondary muscle spindle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496447
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637684
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12526770
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12526770
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702645
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496447
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001080	defasiculated phrenic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496447
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637684
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001084	abnormal petrosal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001102	small superior vagus ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001107	decreased Schwann cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12526770
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12526770
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18381417
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702645
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496447
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809799
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20150924	MGI			PMID:25269082
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12526770
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20150924	MGI			PMID:12955145
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20150924	MGI			PMID:25269082
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496447
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702645
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702645
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716706
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12526770
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809799
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20150924	MGI			PMID:12955145
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12526770
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496447
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051890
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702645
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637684
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25269082
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20150924	MGI			PMID:25269082
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25269082
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20150924	MGI			PMID:12955145
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702645
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0004075	decreased Schwann cell precursor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637684
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250911	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637684
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044753
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0008317	abnormal paravertebral ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809799
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0008317	abnormal paravertebral ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051890
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0008468	absent muscle spindles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702645
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0008486	decreased muscle spindle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20231221	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0009505	abnormal mammary gland lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051890
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051890
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18381417
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0010493	abnormal atrium myocardium morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25269082
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20150924	MGI			PMID:25269082
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072561
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496447
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704452
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477377
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637684
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564761
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809799
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051890
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362461
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20150924	MGI			PMID:16466971
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20150924	MGI			PMID:25269082
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496447
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0014317	decreased heart left ventricle septal wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:19954518
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0030972	increased myoblast apoptosis		IAGP		N	RGD:5509061	20211125	MGI			PMID:12052879
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:11984589
10533	Erbb2	erb-b2 receptor tyrosine kinase 2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:12072561
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20200402	MGI			
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0000478	delayed intestine development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082767
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0001664	abnormal digestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082767
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082767
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0002691	small stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20200402	MGI			
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20200402	MGI			
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200402	MGI			
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20200402	MGI			
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0005653	phototoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10022922
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0005653	phototoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082767
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082767
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10534	Ercc5	excision repair cross-complementing rodent repair deficiency, complementation group 5	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20241121	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20241121	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20241121	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20241121	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20241121	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20240307	MGI			PMID:3101673
10536	Ces1c	carboxylesterase 1C	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20240307	MGI			PMID:7236294
10536	Ces1c	carboxylesterase 1C	gene	MP:0005534	decreased body temperature		IEA		N	RGD:5509061	20111116	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20240307	MGI			PMID:10945631
10536	Ces1c	carboxylesterase 1C	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20240307	MGI			PMID:3101673
10536	Ces1c	carboxylesterase 1C	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IEA		N	RGD:5509061	20111116	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IEA		N	RGD:5509061	20111116	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20241121	MGI			
10536	Ces1c	carboxylesterase 1C	gene	MP:0013275	abnormal xenobiotic metabolism		IAGP		N	RGD:5509061	20240307	MGI			PMID:10945631
10536	Ces1c	carboxylesterase 1C	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
10550	Esd	esterase D/formylglutathione hydrolase	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
10550	Esd	esterase D/formylglutathione hydrolase	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
10550	Esd	esterase D/formylglutathione hydrolase	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667977
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803905
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053716
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20150319	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647203
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160157
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785410
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213494
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919287
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019156
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574448
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667977
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213494
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785410
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510352
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391155
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974921
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20180830	MGI			PMID:29122548
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20180830	MGI			PMID:29122548
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001123	dilated uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919287
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342864
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342864
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919287
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149719
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20180830	MGI			PMID:29122548
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001139	abnormal vagina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001140	abnormal vagina epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10670526
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8723431
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755802
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755802
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8723431
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10558910
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17495854
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667977
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593044
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:24739975
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001356	increased aggression towards female mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114183
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001356	increased aggression towards female mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832446
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24739975
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001376	abnormal mating receptivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001376	abnormal mating receptivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832446
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832446
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832446
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832446
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832446
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9037078
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444817
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803905
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053716
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297545
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14583652
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667977
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149719
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444817
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785410
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213494
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001884	mammary gland alveolar hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213494
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001885	mammary gland duct hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213494
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188600
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20180830	MGI			PMID:29122548
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698654
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755802
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17947360
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574448
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17947360
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149719
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20220407	MGI			PMID:21149719
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053716
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875230
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875230
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20577047
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141204	MGI			
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444817
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9037078
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10670526
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574448
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10670526
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755802
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285805
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593044
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10558910
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149719
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17495854
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17495854
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755802
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667977
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444817
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667977
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17495854
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:10558910
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20180830	MGI			PMID:29122548
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003572	abnormal uterus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667977
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755802
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557741
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:17495854
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:18063692
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188600
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444817
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393999
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510352
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444817
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114183
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:24739975
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003969	abnormal luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0003969	abnormal luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074057
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:15283680
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775144
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10558910
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10558910
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004728	abnormal efferent ductules of testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10670526
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342864
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919287
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574448
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004850	abnormal testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393999
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755802
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20577047
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004894	uterus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160157
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755802
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004902	abnormal uterus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974921
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004903	abnormal uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557741
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10558910
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557741
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17495854
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10670526
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393999
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510352
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803905
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053716
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444817
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15283680
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803905
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875230
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919287
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005133	increased luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17495854
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444817
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8584021
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19366879
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19366879
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160157
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160157
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188600
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285805
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19366879
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005646	abnormal pituitary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171231
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:9037078
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0006416	abnormal rete testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0006423	dilated rete testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698654
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0006423	dilated rete testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0006423	dilated rete testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393999
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875230
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647203
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875230
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647203
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008256	abnormal myometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008332	decreased lactotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171231
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008334	increased gonadotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008335	decreased gonadotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439729
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008487	abnormal mesonephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11014235
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008737	abnormal spleen physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919287
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317592
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008983	small vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008984	vagina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008984	vagina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008984	vagina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008994	early vaginal opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149719
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149719
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009097	absent endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009130	increased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009140	dilated efferent ductule of testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10670526
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009140	dilated efferent ductule of testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698654
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009140	dilated efferent ductule of testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393999
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009205	abnormal internal male genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8723431
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009251	enlarged endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009257	dilated seminiferous tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009257	dilated seminiferous tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444817
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009296	increased mammary fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009300	increased parametrial fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009359	endometrium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009363	abnormal tertiary ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009363	abnormal tertiary ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009363	abnormal tertiary ovarian follicle morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009365	abnormal theca cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009365	abnormal theca cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009370	decreased theca cell number		IAGP		N	RGD:5509061	20220407	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009371	increased theca cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009371	increased theca cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342864
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919287
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149719
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248223
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20220407	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20220407	MGI			PMID:17947360
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20220407	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785410
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009662	abnormal uterine receptivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974921
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351685
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070086
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009697	abnormal copulation behavior		IAGP		N	RGD:5509061	20240718	MGI			PMID:11114183
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009736	abnormal prostate gland branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755802
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009824	spermatic granuloma		IAGP		N	RGD:5509061	20141003	MGI			PMID:10670526
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213494
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019156
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009856	failure of ejaculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114183
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0009856	failure of ejaculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9037078
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667977
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019156
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010962	decreased compact bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053716
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010967	increased compact bone area		IAGP		N	RGD:5509061	20141003	MGI			PMID:15283680
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20150319	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873215
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24371309
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:17046690
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:18339713
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17495854
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:17495854
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0011833	abnormal cremaster muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8723431
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0013613	abnormal volumetric bone mineral density		IAGP		N	RGD:5509061	20150319	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0013615	increased volumetric bone mineral density		IAGP		N	RGD:5509061	20150319	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0013616	decreased volumetric bone mineral density		IAGP		N	RGD:5509061	20150319	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20150319	MGI			PMID:16234973
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20220915	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:17332369
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20190207	MGI			PMID:28314781
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:22800760
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:17803905
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160616	MGI			PMID:17803905
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:15283680
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0020080	increased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:17803905
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:15283680
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:14745006
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0021182	decreased femoral compact bone area		IAGP		N	RGD:5509061	20220922	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0030985	decreased circulating osteocalcin level		IAGP		N	RGD:5509061	20201001	MGI			PMID:10805804
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:10976058
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:18953638
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:19423761
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220630	MGI			PMID:10342864
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0031436	decreased copulatory plug deposition		IAGP		N	RGD:5509061	20240718	MGI			PMID:8895349
10551	Esr1	estrogen receptor 1 (alpha)	gene	MP:0031628	abnormal intromission		IAGP		N	RGD:5509061	20240718	MGI			PMID:9037078
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733032
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15375213
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15375213
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781739
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000392	accelerated hair follicle regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591132
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16477031
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522255
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522255
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226319
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226319
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226319
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20170504	MGI			PMID:25848008
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20170504	MGI			PMID:25848008
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591132
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781739
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114183
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001356	increased aggression towards female mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114183
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593044
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15642619
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593044
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15642619
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891272
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054246
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15375213
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14583652
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001884	mammary gland alveolar hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438700
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141204	MGI			PMID:23580569
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268329
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268329
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20170504	MGI			PMID:25848008
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268329
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226319
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002208	abnormal germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044378
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14612399
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114183
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268329
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10600740
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285805
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593044
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593044
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16477031
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20150618	MGI			PMID:17332369
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781739
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11799247
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19366879
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15283680
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733032
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054246
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11799247
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19366879
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226319
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226319
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:23580569
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:10927637
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557741
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114183
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11799247
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535856
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:14753739
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535856
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15698835
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317592
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004746	abnormal cochlear IHC afferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062753
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14612399
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12603601
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16477031
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593044
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004903	abnormal uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557741
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557741
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19366879
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15283680
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781739
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285805
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19366879
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19366879
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10927637
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11799247
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11799247
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15280152
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15642619
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15375213
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438700
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438700
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0006416	abnormal rete testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15375213
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11380688
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535856
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008532	decreased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:17980496
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226319
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591132
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20170504	MGI			PMID:25848008
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15698835
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16477031
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16477031
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226319
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008983	small vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0008984	vagina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19366879
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009257	dilated seminiferous tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009363	abnormal tertiary ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009363	abnormal tertiary ovarian follicle morphology		IAGP		N	RGD:5509061	20170504	MGI			PMID:25848008
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009370	decreased theca cell number		IAGP		N	RGD:5509061	20220407	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009372	abnormal cumulus oophorus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20220407	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054246
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054246
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438700
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591132
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009646	urinary bladder inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522255
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009648	abnormal superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009697	abnormal copulation behavior		IAGP		N	RGD:5509061	20240718	MGI			PMID:11114183
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781739
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0009856	failure of ejaculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114183
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095962
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535856
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:15642619
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332369
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0010386	abnormal urinary bladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522255
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0010967	increased compact bone area		IAGP		N	RGD:5509061	20141003	MGI			PMID:15283680
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805804
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522255
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740446
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0013616	decreased volumetric bone mineral density		IAGP		N	RGD:5509061	20150319	MGI			PMID:17535856
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20220915	MGI			PMID:10805804
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:17332369
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0014234	decreased enterocyte apoptosis		IAGP		N	RGD:5509061	20230323	MGI			PMID:16477031
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:15375213
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0015067	increased myocardial fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:15375213
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:10805804
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0021182	decreased femoral compact bone area		IAGP		N	RGD:5509061	20220922	MGI			PMID:10805804
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0030985	decreased circulating osteocalcin level		IAGP		N	RGD:5509061	20201002	MGI			PMID:10805804
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:10976058
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:18268329
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:25848008
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031383	increased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:25848008
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220630	MGI			PMID:23580569
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:18268329
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:9861029
10552	Esr2	estrogen receptor 2 (beta)	gene	MP:0031650	decreased mounting behavior		IAGP		N	RGD:5509061	20240905	MGI			PMID:11114183
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000370	head blaze		IEA		N	RGD:5509061	20160128	MGI			
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496469
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496469
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818745
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0002369	abnormal thymus subcapsular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0002938	white spotting		IEA		N	RGD:5509061	20160128	MGI			
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818745
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818745
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818745
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818745
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0009322	increased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0010428	abnormal heart right ventricle outflow tract morphology		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384043
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496469
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806641
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339335
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0012745	abnormal neural crest cell physiology		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0012749	decreased cardiac neural crest cell number		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
10554	Ets1	Ets proto-oncogene 1, transcription factor	gene	MP:0020321	increased vascular endothelial cell apoptosis		IAGP		N	RGD:5509061	20160616	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0000399	increased curvature of guard hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0000401	increased curvature of awl hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0000403	increased curvature of zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0000406	increased curvature of auchene hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007139
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977525
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977525
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:14612405
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977525
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485465
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14612405
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19847259
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977525
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19847259
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007139
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19847259
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977525
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977525
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573048
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14612405
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411629
10555	Ets2	Ets proto-oncogene 2, transcription factor	gene	MP:0020321	increased vascular endothelial cell apoptosis		IAGP		N	RGD:5509061	20160616	MGI			PMID:19411629
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918574
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967980
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632823
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632823
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17623652
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757438
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8972001
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305483
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120874
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14980205
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003228	abnormal sinus venosus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967980
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632823
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632823
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0004181	abnormal carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591683
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591683
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0005085	abnormal gallbladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431214
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11850418
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632823
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0006315	abnormal urine protein level		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305483
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305483
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305483
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363687
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305483
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345469
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757438
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0010695	abnormal blood pressure regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8972001
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0010697	abnormal systemic arterial blood pressure regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8972001
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0010874	abnormal bone volume		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0010964	increased compact bone volume		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632823
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8972001
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20160804	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0021030	decreased tumor necrosis factor (ligand) superfamily member 11 level		IAGP		N	RGD:5509061	20211230	MGI			PMID:25460576
10556	F2r	coagulation factor II thrombin receptor	gene	MP:0021032	increased tumor necrosis factor receptor superfamily member 11b level		IAGP		N	RGD:5509061	20211230	MGI			PMID:25460576
10557	F5	coagulation factor V	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200917	MGI			PMID:8900278
10557	F5	coagulation factor V	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8900278
10557	F5	coagulation factor V	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10557	F5	coagulation factor V	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8900278
10557	F5	coagulation factor V	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:8900278
10557	F5	coagulation factor V	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10829076
10557	F5	coagulation factor V	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10557	F5	coagulation factor V	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8900278
10557	F5	coagulation factor V	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344422
10557	F5	coagulation factor V	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10829076
10557	F5	coagulation factor V	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110695
10557	F5	coagulation factor V	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110695
10557	F5	coagulation factor V	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110695
10557	F5	coagulation factor V	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10829076
10557	F5	coagulation factor V	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110695
10557	F5	coagulation factor V	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110695
10557	F5	coagulation factor V	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10557	F5	coagulation factor V	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10557	F5	coagulation factor V	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20251023	MGI			PMID:40455764
10557	F5	coagulation factor V	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344422
10557	F5	coagulation factor V	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20251023	MGI			PMID:40455764
10557	F5	coagulation factor V	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344422
10557	F5	coagulation factor V	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20180322	MGI			PMID:28827327
10557	F5	coagulation factor V	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8900278
10557	F5	coagulation factor V	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10829076
10557	F5	coagulation factor V	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11533492
10557	F5	coagulation factor V	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20180322	MGI			PMID:28827327
10557	F5	coagulation factor V	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8900278
10557	F5	coagulation factor V	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180322	MGI			PMID:11110695
10557	F5	coagulation factor V	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180322	MGI			PMID:28827327
10557	F5	coagulation factor V	gene	MP:0011514	skin hemorrhage		IAGP		N	RGD:5509061	20200917	MGI			PMID:8900278
10557	F5	coagulation factor V	gene	MP:0012356	increased prothrombin time		IAGP		N	RGD:5509061	20251023	MGI			PMID:40455764
10557	F5	coagulation factor V	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20251023	MGI			PMID:40455764
10559	F9	coagulation factor IX	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19583826
10559	F9	coagulation factor IX	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354664
10559	F9	coagulation factor IX	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354664
10559	F9	coagulation factor IX	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354664
10559	F9	coagulation factor IX	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9639513
10559	F9	coagulation factor IX	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354664
10559	F9	coagulation factor IX	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19583826
10559	F9	coagulation factor IX	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326649
10559	F9	coagulation factor IX	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354664
10559	F9	coagulation factor IX	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9639513
10559	F9	coagulation factor IX	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20180913	MGI			PMID:26964564
10559	F9	coagulation factor IX	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326649
10559	F9	coagulation factor IX	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178576
10559	F9	coagulation factor IX	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:19583826
10559	F9	coagulation factor IX	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326649
10559	F9	coagulation factor IX	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:9639513
10559	F9	coagulation factor IX	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19583826
10559	F9	coagulation factor IX	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9639513
10559	F9	coagulation factor IX	gene	MP:0012305	umbilical cord hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9639513
10559	F9	coagulation factor IX	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20180913	MGI			PMID:26964564
10559	F9	coagulation factor IX	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20180913	MGI			PMID:26964564
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534295
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670956
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534295
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534295
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0002139	abnormal hepatobiliary system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670956
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534295
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20210128	MGI			
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534295
10563	Fabp1	fatty acid binding protein 1, liver	gene	MP:0012361	decreased large unstained cell number		IEA		N	RGD:5509061	20201022	MGI			
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210826	MGI			
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10564	Fabp2	fatty acid binding protein 2, intestinal	gene	MP:0009307	decreased uterine fat pad weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:11023988
10565	Fabp6	fatty acid binding protein 6	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23251388
10565	Fabp6	fatty acid binding protein 6	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23251388
10565	Fabp6	fatty acid binding protein 6	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23251388
10565	Fabp6	fatty acid binding protein 6	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23251388
10565	Fabp6	fatty acid binding protein 6	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23251388
10565	Fabp6	fatty acid binding protein 6	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23251388
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9596654
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630504
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0005158	ovary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8704201
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20022886
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0008404	increased cellular sensitivity to methylmethanesulfonate induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9596654
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9596654
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20260402	MGI			
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:20022886
10566	Fancc	Fanconi anemia, complementation group C	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:11493445
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165533
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165533
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8252632
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062348
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0002531	abnormal type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8759751
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:8759751
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0003423	reduced thrombolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9586641
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165533
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062348
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8252632
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8759751
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
10570	Fcer1a	Fc receptor, IgE, high affinity I, alpha polypeptide	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165533
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251634
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001588	abnormal hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258336
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313472
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739057
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001819	abnormal immune cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313472
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739057
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313472
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776906
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911824
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062348
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062348
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16246361
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576552
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17446931
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004828	decreased susceptibility to autoimmune hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17317854
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004867	decreased platelet calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12586747
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20664169
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021533
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9396764
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17446931
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313472
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062348
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005614	decreased susceptibility to type III hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12586747
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9396764
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008352	absent gamma-delta intraepithelial T cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529325
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073337
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493731
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9396764
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493731
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493731
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493731
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008680	abnormal interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843660
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008691	decreased interleukin-23 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493731
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493731
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20191128	MGI			PMID:27887882
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776906
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258336
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0008876	decreased uterine NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16246361
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20554973
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739057
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0010138	arteritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313472
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9396764
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0012529	abnormal decidua basalis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0012726	abnormal uterine spiral artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0012727	abnormal uterine spiral artery remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
10572	Fcer1g	Fc receptor, IgE, high affinity I, gamma polypeptide	gene	MP:0030072	round face		IAGP		N	RGD:5509061	20170921	MGI			PMID:15073337
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911823
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911824
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911823
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474370
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911824
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002421	abnormal cell-mediated immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911823
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911824
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002454	abnormal macrophage antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911823
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911824
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892619
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911823
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0002531	abnormal type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911824
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911824
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0004828	decreased susceptibility to autoimmune hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911824
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
10573	Fcgr1	Fc receptor, IgG, high affinity I	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892619
10576	Fga	fibrinogen alpha chain	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
10576	Fga	fibrinogen alpha chain	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11906694
10576	Fga	fibrinogen alpha chain	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
10576	Fga	fibrinogen alpha chain	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
10576	Fga	fibrinogen alpha chain	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10930441
10576	Fga	fibrinogen alpha chain	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
10576	Fga	fibrinogen alpha chain	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
10576	Fga	fibrinogen alpha chain	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
10576	Fga	fibrinogen alpha chain	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
10576	Fga	fibrinogen alpha chain	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275201
10576	Fga	fibrinogen alpha chain	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0004898	uterine hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
10576	Fga	fibrinogen alpha chain	gene	MP:0005245	hemarthrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10930441
10576	Fga	fibrinogen alpha chain	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
10576	Fga	fibrinogen alpha chain	gene	MP:0011514	skin hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0012330	decreased circulating fibrinogen level		IAGP		N	RGD:5509061	20200625	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0020215	impaired blood coagulation		IAGP		N	RGD:5509061	20200625	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0031137	vaginal hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0031152	subcutaneous hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:7649481
10576	Fga	fibrinogen alpha chain	gene	MP:0031153	stomach hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:8929539
10577	Fgf1	fibroblast growth factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688672
10577	Fgf1	fibroblast growth factor 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688672
10577	Fgf1	fibroblast growth factor 1	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688672
10577	Fgf1	fibroblast growth factor 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688672
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16513252
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20250508	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000486	abnormal pulmonary trunk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16956603
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16956603
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000537	abnormal urethra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340846
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810586
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340846
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19407009
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20171206
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719891
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000551	absent forelimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000551	absent forelimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000551	absent forelimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000551	absent forelimb		IAGP		N	RGD:5509061	20150903	MGI			PMID:25468972
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719891
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810586
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20171206
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000614	absent salivary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000618	small salivary gland		IAGP		N	RGD:5509061	20210128	MGI			PMID:26321752
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20210128	MGI			PMID:26321752
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000624	xerostomia		IAGP		N	RGD:5509061	20210128	MGI			PMID:26321752
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782400
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10578	Fgf10	fibroblast growth factor 10	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941620
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941620
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001159	absent prostate gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941620
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388344
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388344
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21742743
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19407009
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19407009
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20230601	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20230601	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001347	absent lacrimal glands		IAGP		N	RGD:5509061	20181220	MGI			PMID:10964474
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20210128	MGI			PMID:26321752
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20171206
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720875
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20171206
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20171206
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20171206
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002295	abnormal pulmonary circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002297	abnormal forced expiratory flow rates		IAGP		N	RGD:5509061	20141003	MGI			PMID:21742743
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20210128	MGI			PMID:26321752
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002691	small stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002729	abnormal inner ear canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002770	absent bulbourethral gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941620
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19407009
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810586
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843416
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003163	absent posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003165	absent superior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800000
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19407009
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003334	pancreas fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003595	epididymal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941620
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800000
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941620
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003760	decreased palatal length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003827	abnormal Wolffian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941620
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388344
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623822
10578	Fgf10	fibroblast growth factor 10	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004035	abnormal sublingual gland morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:26321752
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004309	absent otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810586
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004309	absent otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20171206
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810586
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623822
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20171206
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004313	absent vestibulocochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623822
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004317	small vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004352	absent humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004360	absent ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004830	short incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16956603
10578	Fgf10	fibroblast growth factor 10	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:19407009
10578	Fgf10	fibroblast growth factor 10	gene	MP:0005314	absent thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0005315	absent pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810586
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19407009
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20230601	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388344
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006285	absent inner ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810586
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0008320	absent adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0008786	abnormal hindgut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16956603
10578	Fgf10	fibroblast growth factor 10	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0008881	absent Harderian gland		IAGP		N	RGD:5509061	20181220	MGI			PMID:10964474
10578	Fgf10	fibroblast growth factor 10	gene	MP:0008904	abnormal mammary fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782400
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009479	abnormal cecum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14697353
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009479	abnormal cecum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308329
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009479	abnormal cecum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16956603
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009479	abnormal cecum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719891
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009509	absent rectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009510	cecal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009510	cecal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719891
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009520	decreased submandibular gland size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972105
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009520	decreased submandibular gland size		IAGP		N	RGD:5509061	20210128	MGI			PMID:26321752
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009522	submandibular gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972105
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009524	absent submandibular gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009524	absent submandibular gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972105
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009525	abnormal submandibular duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972105
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009571	abnormal right lung accessory lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009572	abnormal right lung cranial lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009573	abnormal right lung middle lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009884	palatal shelf fusion with tongue or mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10578	Fgf10	fibroblast growth factor 10	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010116	abnormal primitive urogenital sinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941620
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010489	abnormal heart atrium auricular region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010521	absent pulmonary artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010646	absent pulmonary vein		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010794	abnormal stomach submucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010906	abnormal lung bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719891
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010907	absent lung buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719891
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010907	absent lung buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010975	abnormal lung lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0010976	small lung lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011025	abnormal branching involved in trachea morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800000
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011030	impaired branching involved in preterminal bronchiole morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011064	abnormal vestibular hair cell kinocilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761848
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916808
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19407009
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623822
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011305	dilated kidney calyx		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011332	abnormal kidney outer medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011333	abnormal kidney inner medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011457	abnormal metanephric ureteric bud development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011759	absent Rathke's pouch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0011884	absent colon		IAGP		N	RGD:5509061	20160304	MGI			PMID:16956603
10578	Fgf10	fibroblast growth factor 10	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013264	tongue ankylosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013268	second pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013269	third pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013338	abnormal neurohypophysis development		IAGP		N	RGD:5509061	20141211	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013352	abnormal Rathke's pouch apoptosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013445	Harderian gland atrophy		IAGP		N	RGD:5509061	20150205	MGI			PMID:19407009
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013495	decreased trachea gland number		IAGP		N	RGD:5509061	20150305	MGI			PMID:15973734
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013531	abnormal periderm development		IAGP		N	RGD:5509061	20150219	MGI			PMID:16720875
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013541	abnormal submandibular gland development		IAGP		N	RGD:5509061	20210128	MGI			PMID:26321752
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013580	abnormal nasal gland morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27590203
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013582	abnormal lateral nasal gland morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27590203
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013721	abnormal mammary placode morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:11782400
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013721	abnormal mammary placode morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:16720875
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013766	absent palatal rugae		IAGP		N	RGD:5509061	20150430	MGI			PMID:15199404
10578	Fgf10	fibroblast growth factor 10	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160304	MGI			PMID:16956603
10578	Fgf10	fibroblast growth factor 10	gene	MP:0014958	decreased lung enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:15800000
10578	Fgf10	fibroblast growth factor 10	gene	MP:0015006	decreased fetal length		IAGP		N	RGD:5509061	20260611	MGI			PMID:9784490
10578	Fgf10	fibroblast growth factor 10	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
10578	Fgf10	fibroblast growth factor 10	gene	MP:0021206	abnormal limb muscle morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:12388344
10578	Fgf10	fibroblast growth factor 10	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:15199404
10578	Fgf10	fibroblast growth factor 10	gene	MP:0030920	small hair follicle bulb		IAGP		N	RGD:5509061	20181220	MGI			PMID:11062007
10578	Fgf10	fibroblast growth factor 10	gene	MP:0031300	perineal hypospadia		IAGP		N	RGD:5509061	20211014	MGI			PMID:15234214
10578	Fgf10	fibroblast growth factor 10	gene	MP:0031343	colon atresia		IAGP		N	RGD:5509061	20220217	MGI			PMID:22719891
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15621532
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20160811	MGI			
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000494	abnormal cecum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308329
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18653563
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19219044
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16496342
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858205
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858205
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18653563
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16496342
10579	Fgf9	fibroblast growth factor 9	gene	MP:0001956	hypopnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858205
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16496342
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15621532
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15621532
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15621532
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20160421	MGI			
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0002996	ovotestis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003189	fused joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003189	fused joints		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003200	calcified joint		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20160811	MGI			
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003416	premature bone ossification		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:16496342
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16496342
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003742	narrow head		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0003758	narrow palate		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004676	wide ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18653563
10579	Fgf9	fibroblast growth factor 9	gene	MP:0004932	epididymis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858205
10579	Fgf9	fibroblast growth factor 9	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818193
10579	Fgf9	fibroblast growth factor 9	gene	MP:0006418	abnormal testis cord formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0006419	disorganized testis cords		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0006421	decreased number of peritubular myoid cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0008159	increased diameter of fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0008161	increased diameter of radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0008162	increased diameter of tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0008163	increased diameter of ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15621532
10579	Fgf9	fibroblast growth factor 9	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0009880	decreased mouth size		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0009891	abnormal palate bone morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0009906	increased tongue size		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0010114	abnormal coccyx morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16496342
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16496342
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011142	abnormal lung-associated mesenchyme development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540513
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011146	abnormal mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493531
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:15621532
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011692	increased chondrocyte number		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818193
10579	Fgf9	fibroblast growth factor 9	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20171214	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0013550	abnormal secondary palate morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0013602	abnormal Leydig cell differentiation		IAGP		N	RGD:5509061	20150319	MGI			PMID:11290325
10579	Fgf9	fibroblast growth factor 9	gene	MP:0014299	increased cochlea size		IAGP		N	RGD:5509061	20241031	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0014430	decreased hyaluronic acid level		IAGP		N	RGD:5509061	20240425	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0014562	increased tympanic ring size		IAGP		N	RGD:5509061	20241031	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0030032	high forehead		IAGP		N	RGD:5509061	20170810	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171116	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171116	MGI			PMID:19219044
10579	Fgf9	fibroblast growth factor 9	gene	MP:0030354	premature sagittal suture closure		IAGP		N	RGD:5509061	20171116	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0030372	enlarged Meckel's cartilage		IAGP		N	RGD:5509061	20171207	MGI			PMID:12140681
10579	Fgf9	fibroblast growth factor 9	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20180628	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0030837	abnormal knee joint morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:28169396
10579	Fgf9	fibroblast growth factor 9	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:21858205
10579	Fgf9	fibroblast growth factor 9	gene	MP:0031306	abnormal cartilage physiology		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221117	MGI			PMID:33959039
10579	Fgf9	fibroblast growth factor 9	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:33959039
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934262
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000035	abnormal membranous labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934262
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934262
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:25966306
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297725
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000324	increased mast cell number		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20170907	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20260305	MGI			PMID:41390905
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20160915	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18653563
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581874
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21128305
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581874
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141127	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000537	abnormal urethra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340846
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000537	abnormal urethra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843416
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340846
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20150219	MGI			PMID:24956260
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000551	absent forelimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000551	absent forelimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000629	absent mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782400
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000648	absent sebaceous gland		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000649	sebaceous gland atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000666	decreased prostate gland duct number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12666202
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141127	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418794
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20077479
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20150219	MGI			PMID:24956260
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720875
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418794
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20260305	MGI			PMID:41390905
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001347	absent lacrimal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077586
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001347	absent lacrimal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18653563
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001669	abnormal intestinal glucose absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17150206
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001677	absent apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560232
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001725	abnormal umbilical cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12666202
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:3181757
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560232
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715082
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20077479
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17150206
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180705	MGI			PMID:25264521
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715082
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002295	abnormal pulmonary circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934262
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560232
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002691	small stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297725
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20260305	MGI			PMID:41390905
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581874
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20150219	MGI			PMID:24956260
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003085	abnormal egg cylinder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560232
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003108	short zygomatic bone		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843416
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003189	fused joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934262
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003315	abnormal perineum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003418	premature intramembranous bone ossification		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934262
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003760	decreased palatal length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003760	decreased palatal length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141218	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003840	abnormal coronal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003840	abnormal coronal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003840	abnormal coronal suture morphology		IAGP		N	RGD:5509061	20260305	MGI			PMID:41390905
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003841	abnormal lambdoid suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003843	abnormal sagittal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003843	abnormal sagittal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003843	abnormal sagittal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560232
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559489
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141127	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004032	abnormal interventricular groove morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004053	abnormal synchondrosis		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20150219	MGI			PMID:24956260
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559489
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934262
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004346	absent acromion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004451	short presphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004451	short presphenoid bone		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20160915	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581874
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004507	abnormal ischium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004537	abnormal palatine bone horizontal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004552	fused tracheal cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004606	absent vertebral spinous process		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004691	absent pubis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418794
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418794
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004831	long incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18653563
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581874
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21128305
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004961	increased prostate gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12666202
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560232
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20077479
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005314	absent thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0005354	abnormal ilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934262
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581874
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20150219	MGI			PMID:24956260
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006213	shallow orbits		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006213	shallow orbits		IAGP		N	RGD:5509061	20171019	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006213	shallow orbits		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006213	shallow orbits		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006287	inner ear cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006399	abnormal long bone epiphyseal ossification zone morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008320	absent adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008320	absent adenohypophysis		IAGP		N	RGD:5509061	20141127	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20170907	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008534	enlarged fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20077479
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20077479
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20077479
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008785	abnormal sternum manubrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009003	abnormal vibrissa number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009004	progressive hair loss		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009004	progressive hair loss		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009051	dilated distal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009479	abnormal cecum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14697353
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009509	absent rectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009510	cecal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15234214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009520	decreased submandibular gland size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972105
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009522	submandibular gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972105
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009524	absent submandibular gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009524	absent submandibular gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972105
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009524	absent submandibular gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009525	abnormal submandibular duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972105
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009545	abnormal dermis papillary layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009570	abnormal right lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009601	epidermis stratum granulosum hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009611	epidermis stratum spinosum hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009736	abnormal prostate gland branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12666202
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009884	palatal shelf fusion with tongue or mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010422	heart right ventricle hypoplasia		IAGP		N	RGD:5509061	20231221	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010521	absent pulmonary artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010587	conotruncal ridge hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010646	absent pulmonary vein		IAGP		N	RGD:5509061	20141003	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010647	heart left atrium hypoplasia		IAGP		N	RGD:5509061	20231221	MGI			PMID:16687131
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010678	abnormal skin adnexa morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010911	abnormal pulmonary acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010979	small ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010979	small ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:21128305
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010980	ectopic ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010980	ectopic ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:21128305
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010982	abnormal ureteric bud elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21128305
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21128305
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010994	aerophagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0010998	pulmonary alveolar proteinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011011	impaired lung lobe morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011011	impaired lung lobe morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011013	bronchiolectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011026	impaired branching involved in trachea morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19618463
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418794
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17150206
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560232
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756187
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435295
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011158	absent hypodermis muscle layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011185	absent primitive endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560232
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21128305
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011387	absent metanephric mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16442091
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011485	abnormal urethra urothelium morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20170907	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011627	decreased skin pigmentation		IAGP		N	RGD:5509061	20171207	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011696	absent mast cells		IAGP		N	RGD:5509061	20150716	MGI			PMID:25843682
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011759	absent Rathke's pouch		IAGP		N	RGD:5509061	20141218	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011772	genital tubercle hypoplasia		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011861	increased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011861	increased cranium height		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011861	increased cranium height		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20170907	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20160915	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012270	cardiac edema		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012667	split sternal manubrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0012683	absent telencephalon		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013192	decreased sebaceous gland number		IAGP		N	RGD:5509061	20150716	MGI			PMID:20308431
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013264	tongue ankylosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199404
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013310	abnormal adrenal gland development		IAGP		N	RGD:5509061	20141127	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013317	abnormal seminal vesicle development		IAGP		N	RGD:5509061	20141204	MGI			PMID:12666202
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013318	abnormal branching involved in seminal vesicle morphogenesis		IAGP		N	RGD:5509061	20141204	MGI			PMID:17202188
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013331	abnormal lacrimal gland development		IAGP		N	RGD:5509061	20141204	MGI			PMID:18077586
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013351	abnormal Rathke's pouch development		IAGP		N	RGD:5509061	20141218	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013352	abnormal Rathke's pouch apoptosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013470	absent lacrimal gland bud		IAGP		N	RGD:5509061	20150319	MGI			PMID:18077586
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013578	abnormal stomach glandular region morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013580	abnormal nasal gland morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27590203
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013582	abnormal lateral nasal gland morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27590203
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013721	abnormal mammary placode morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:16720875
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013766	absent palatal rugae		IAGP		N	RGD:5509061	20150430	MGI			PMID:15199404
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013785	abnormal mammary gland bud morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:11782400
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0013904	abnormal seminal vesicle muscle layer morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:12666202
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0014051	abnormal maxillary-premaxillary suture morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0014152	absent exorbital lacrimal gland		IAGP		N	RGD:5509061	20160407	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0020386	adipose tissue inflammation		IAGP		N	RGD:5509061	20171207	MGI			PMID:17304214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:15199404
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030064	small face		IAGP		N	RGD:5509061	20170921	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20171207	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20171207	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20260305	MGI			PMID:41390905
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030076	abnormal cranial cavity morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030167	decreased inner canthal distance		IAGP		N	RGD:5509061	20171005	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030194	abnormal intermaxillary suture morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030196	abnormal nasomaxillary suture morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030200	abnormal nasal septum cartilage morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030205	thick nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030250	frontonasal prominence hypoplasia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030265	parietal bossing		IAGP		N	RGD:5509061	20171109	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030274	maxillary retrognathia		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030275	thin frontal bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030281	thin parietal bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030301	abnormal maxillary frontal process morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030301	abnormal maxillary frontal process morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030302	abnormal maxillary zygomatic process morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030302	abnormal maxillary zygomatic process morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030315	small neurocranium		IAGP		N	RGD:5509061	20171109	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171116	MGI			PMID:14499350
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171116	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171116	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:11274405
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:17132737
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:20077479
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:25966306
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171214	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20260305	MGI			PMID:41390905
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030353	wide sagittal suture		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030356	premature lambdoid suture closure		IAGP		N	RGD:5509061	20171214	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030358	premature squamoparietal suture closure		IAGP		N	RGD:5509061	20171116	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030358	premature squamoparietal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:10631169
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030371	delayed sagittal suture closure		IAGP		N	RGD:5509061	20260305	MGI			PMID:41390905
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030375	short zygomatic arch		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030390	premature facial suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030391	premature zygomaticomaxillary suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030391	premature zygomaticomaxillary suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:22585574
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030420	short basicranium		IAGP		N	RGD:5509061	20171214	MGI			PMID:15316116
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030420	short basicranium		IAGP		N	RGD:5509061	20171214	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030420	short basicranium		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030420	short basicranium		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030424	premature palatomaxillary suture closure		IAGP		N	RGD:5509061	20171214	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030425	wide intermaxillary suture		IAGP		N	RGD:5509061	20171214	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20171214	MGI			PMID:15975938
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030434	premature maxillary-premaxillary suture closure		IAGP		N	RGD:5509061	20171214	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030436	premature frontonasal suture closure		IAGP		N	RGD:5509061	20171214	MGI			PMID:21538817
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030437	abnormal osteoblast proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:12135917
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030438	increased osteoblast proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:20175913
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030443	abnormal cranial synchondrosis		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030445	abnormal sphenooccipital synchondrosis		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030446	premature sphenooccipital synchondrosis closure		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030448	premature presphenoid synchondrosis closure		IAGP		N	RGD:5509061	20200521	MGI			PMID:28123344
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030448	premature presphenoid synchondrosis closure		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030464	abnormal cranial cartilage morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:20503384
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030467	abnormal cranial cartilage development		IAGP		N	RGD:5509061	20200514	MGI			PMID:18242159
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20180726	MGI			PMID:11180951
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0031300	perineal hypospadia		IAGP		N	RGD:5509061	20211014	MGI			PMID:15234214
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20260625	MGI			PMID:39158595
10581	Fgfr2	fibroblast growth factor receptor 2	gene	MP:0031525	thin left ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:16687131
10586	Fgg	fibrinogen gamma chain	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434491
10586	Fgg	fibrinogen gamma chain	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980108
10586	Fgg	fibrinogen gamma chain	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891199
10586	Fgg	fibrinogen gamma chain	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891199
10586	Fgg	fibrinogen gamma chain	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891199
10586	Fgg	fibrinogen gamma chain	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891199
10586	Fgg	fibrinogen gamma chain	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891199
10586	Fgg	fibrinogen gamma chain	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980108
10586	Fgg	fibrinogen gamma chain	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173886
10586	Fgg	fibrinogen gamma chain	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173886
10586	Fgg	fibrinogen gamma chain	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980108
10586	Fgg	fibrinogen gamma chain	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434491
10586	Fgg	fibrinogen gamma chain	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0003422	abnormal thrombolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891199
10586	Fgg	fibrinogen gamma chain	gene	MP:0004898	uterine hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891199
10586	Fgg	fibrinogen gamma chain	gene	MP:0004898	uterine hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434491
10586	Fgg	fibrinogen gamma chain	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8918453
10586	Fgg	fibrinogen gamma chain	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:8918453
10586	Fgg	fibrinogen gamma chain	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8918453
10586	Fgg	fibrinogen gamma chain	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17155952
10586	Fgg	fibrinogen gamma chain	gene	MP:0012330	decreased circulating fibrinogen level		IAGP		N	RGD:5509061	20200618	MGI			PMID:15304068
10586	Fgg	fibrinogen gamma chain	gene	MP:0031137	vaginal hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:11891199
10586	Fgg	fibrinogen gamma chain	gene	MP:0031434	increased miscarriage rate		IAGP		N	RGD:5509061	20220915	MGI			PMID:11891199
10587	Fh1	fumarate hydratase 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418408
10587	Fh1	fumarate hydratase 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418408
10587	Fh1	fumarate hydratase 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643539
10587	Fh1	fumarate hydratase 1	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418408
10587	Fh1	fumarate hydratase 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418408
10587	Fh1	fumarate hydratase 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643539
10587	Fh1	fumarate hydratase 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418408
10587	Fh1	fumarate hydratase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418408
10587	Fh1	fumarate hydratase 1	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418408
10587	Fh1	fumarate hydratase 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643539
10587	Fh1	fumarate hydratase 1	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643539
10587	Fh1	fumarate hydratase 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418408
10587	Fh1	fumarate hydratase 1	gene	MP:0011308	kidney corticomedullary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418408
10587	Fh1	fumarate hydratase 1	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20230608	MGI			PMID:23643539
10588	Fhl1	four and a half LIM domains 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20160218	MGI			PMID:25274776
10588	Fhl1	four and a half LIM domains 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160218	MGI			PMID:25274776
10588	Fhl1	four and a half LIM domains 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033658
10588	Fhl1	four and a half LIM domains 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20141003	MGI			
10588	Fhl1	four and a half LIM domains 1	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033658
10588	Fhl1	four and a half LIM domains 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
10588	Fhl1	four and a half LIM domains 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20160218	MGI			PMID:25274776
10588	Fhl1	four and a half LIM domains 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20160218	MGI			PMID:25274776
10588	Fhl1	four and a half LIM domains 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160218	MGI			PMID:25274776
10588	Fhl1	four and a half LIM domains 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20160218	MGI			PMID:25274776
10591	Foxg1	forkhead box G1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
10591	Foxg1	forkhead box G1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
10591	Foxg1	forkhead box G1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:18404215
10591	Foxg1	forkhead box G1	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
10591	Foxg1	forkhead box G1	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0000040	decreased middle ear ossicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0000040	decreased middle ear ossicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
10591	Foxg1	forkhead box G1	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
10591	Foxg1	forkhead box G1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
10591	Foxg1	forkhead box G1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:24043815
10591	Foxg1	forkhead box G1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
10591	Foxg1	forkhead box G1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
10591	Foxg1	forkhead box G1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
10591	Foxg1	forkhead box G1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717732
10591	Foxg1	forkhead box G1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
10591	Foxg1	forkhead box G1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20150129	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441052
10591	Foxg1	forkhead box G1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329011
10591	Foxg1	forkhead box G1	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10591	Foxg1	forkhead box G1	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20230928	MGI			PMID:37075751
10591	Foxg1	forkhead box G1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151532
10591	Foxg1	forkhead box G1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
10591	Foxg1	forkhead box G1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
10591	Foxg1	forkhead box G1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917506
10591	Foxg1	forkhead box G1	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27001178
10591	Foxg1	forkhead box G1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
10591	Foxg1	forkhead box G1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378868
10591	Foxg1	forkhead box G1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
10591	Foxg1	forkhead box G1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
10591	Foxg1	forkhead box G1	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502507
10591	Foxg1	forkhead box G1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502507
10591	Foxg1	forkhead box G1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
10591	Foxg1	forkhead box G1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436615
10591	Foxg1	forkhead box G1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050694
10591	Foxg1	forkhead box G1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
10591	Foxg1	forkhead box G1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0000935	abnormal folding of telencephalic vesicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050694
10591	Foxg1	forkhead box G1	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050694
10591	Foxg1	forkhead box G1	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
10591	Foxg1	forkhead box G1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717732
10591	Foxg1	forkhead box G1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050694
10591	Foxg1	forkhead box G1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0001296	macrophthalmia		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10591	Foxg1	forkhead box G1	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
10591	Foxg1	forkhead box G1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
10591	Foxg1	forkhead box G1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833191
10591	Foxg1	forkhead box G1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
10591	Foxg1	forkhead box G1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
10591	Foxg1	forkhead box G1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:24327562
10591	Foxg1	forkhead box G1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
10591	Foxg1	forkhead box G1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24043815
10591	Foxg1	forkhead box G1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441052
10591	Foxg1	forkhead box G1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
10591	Foxg1	forkhead box G1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837119
10591	Foxg1	forkhead box G1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20260402	MGI			
10591	Foxg1	forkhead box G1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18404215
10591	Foxg1	forkhead box G1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495313
10591	Foxg1	forkhead box G1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20260402	MGI			
10591	Foxg1	forkhead box G1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0002698	abnormal sclera morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
10591	Foxg1	forkhead box G1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487195
10591	Foxg1	forkhead box G1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22120178
10591	Foxg1	forkhead box G1	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0003069	abnormal superior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0003101	high myopia		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0003102	sclera thinning		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495313
10591	Foxg1	forkhead box G1	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0003151	absent tunnel of Corti		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0003152	abnormal pillar cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
10591	Foxg1	forkhead box G1	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0003163	absent posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0003166	decreased superior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0003169	abnormal scala media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18404215
10591	Foxg1	forkhead box G1	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574514
10591	Foxg1	forkhead box G1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574514
10591	Foxg1	forkhead box G1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917506
10591	Foxg1	forkhead box G1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917506
10591	Foxg1	forkhead box G1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
10591	Foxg1	forkhead box G1	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
10591	Foxg1	forkhead box G1	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
10591	Foxg1	forkhead box G1	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
10591	Foxg1	forkhead box G1	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20230831	MGI			PMID:34004180
10591	Foxg1	forkhead box G1	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378868
10591	Foxg1	forkhead box G1	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20230831	MGI			PMID:34004180
10591	Foxg1	forkhead box G1	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
10591	Foxg1	forkhead box G1	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0004236	absent masseter muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0004238	absent pterygoid muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
10591	Foxg1	forkhead box G1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050694
10591	Foxg1	forkhead box G1	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10591	Foxg1	forkhead box G1	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329011
10591	Foxg1	forkhead box G1	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10591	Foxg1	forkhead box G1	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
10591	Foxg1	forkhead box G1	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10591	Foxg1	forkhead box G1	gene	MP:0004282	retrognathia		IAGP		N	RGD:5509061	20171214	MGI			PMID:12717732
10591	Foxg1	forkhead box G1	gene	MP:0004298	vestibular ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0004301	absent organ of Corti supporting cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0004311	otic vesicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0004312	absent pillar cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
10591	Foxg1	forkhead box G1	gene	MP:0004314	absent inner ear vestibule		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0004315	absent vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0004315	absent vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0004329	vestibular saccular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
10591	Foxg1	forkhead box G1	gene	MP:0004330	abnormal vestibular saccular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495313
10591	Foxg1	forkhead box G1	gene	MP:0004332	utricular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
10591	Foxg1	forkhead box G1	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495313
10591	Foxg1	forkhead box G1	gene	MP:0004336	small utricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0004369	absent utricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0004369	absent utricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141228
10591	Foxg1	forkhead box G1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495313
10591	Foxg1	forkhead box G1	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495313
10591	Foxg1	forkhead box G1	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20230831	MGI			PMID:34004180
10591	Foxg1	forkhead box G1	gene	MP:0004403	absent cochlear outer hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0004405	absent cochlear hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0004406	abnormal cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0004408	decreased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0004497	decreased organ of Corti supporting cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141228
10591	Foxg1	forkhead box G1	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:27660326
10591	Foxg1	forkhead box G1	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
10591	Foxg1	forkhead box G1	gene	MP:0004555	pharynx hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0004572	fusion of basioccipital and basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0004572	fusion of basioccipital and basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0004589	abnormal cochlear hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
10591	Foxg1	forkhead box G1	gene	MP:0004900	absent zygomatic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0004922	abnormal common crus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20260402	MGI			
10591	Foxg1	forkhead box G1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151532
10591	Foxg1	forkhead box G1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378868
10591	Foxg1	forkhead box G1	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502507
10591	Foxg1	forkhead box G1	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441052
10591	Foxg1	forkhead box G1	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050694
10591	Foxg1	forkhead box G1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
10591	Foxg1	forkhead box G1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
10591	Foxg1	forkhead box G1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
10591	Foxg1	forkhead box G1	gene	MP:0005195	abnormal posterior eye segment morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0005257	abnormal intraocular pressure		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917506
10591	Foxg1	forkhead box G1	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20161201	MGI			PMID:26670829
10591	Foxg1	forkhead box G1	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151532
10591	Foxg1	forkhead box G1	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:18404215
10591	Foxg1	forkhead box G1	gene	MP:0006024	collapsed Reissner membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833191
10591	Foxg1	forkhead box G1	gene	MP:0006024	collapsed Reissner membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
10591	Foxg1	forkhead box G1	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917506
10591	Foxg1	forkhead box G1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917506
10591	Foxg1	forkhead box G1	gene	MP:0006039	decreased mitochondrial fission		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917506
10591	Foxg1	forkhead box G1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
10591	Foxg1	forkhead box G1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18404215
10591	Foxg1	forkhead box G1	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18404215
10591	Foxg1	forkhead box G1	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20211014	MGI			PMID:25417106
10591	Foxg1	forkhead box G1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0006149	decreased visual acuity		IAGP		N	RGD:5509061	20161117	MGI			PMID:27001178
10591	Foxg1	forkhead box G1	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0006241	abnormal placement of pupils		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917506
10591	Foxg1	forkhead box G1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0006285	absent inner ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0006286	inner ear hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0006289	otic capsule hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0006292	abnormal nasal placode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0006292	abnormal nasal placode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0006331	abnormal patterning of the organ of Corti		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
10591	Foxg1	forkhead box G1	gene	MP:0008035	behavioral arrest		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0008066	small endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487195
10591	Foxg1	forkhead box G1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487195
10591	Foxg1	forkhead box G1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
10591	Foxg1	forkhead box G1	gene	MP:0008285	abnormal hippocampus granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
10591	Foxg1	forkhead box G1	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10591	Foxg1	forkhead box G1	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18404215
10591	Foxg1	forkhead box G1	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
10591	Foxg1	forkhead box G1	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151532
10591	Foxg1	forkhead box G1	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155189
10591	Foxg1	forkhead box G1	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24043815
10591	Foxg1	forkhead box G1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
10591	Foxg1	forkhead box G1	gene	MP:0009690	abnormal neural tube mantle layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151532
10591	Foxg1	forkhead box G1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
10591	Foxg1	forkhead box G1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0009899	hyoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151532
10591	Foxg1	forkhead box G1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27001178
10591	Foxg1	forkhead box G1	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
10591	Foxg1	forkhead box G1	gene	MP:0009974	decreased cerebral cortex pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0010748	abnormal visual evoked potential		IAGP		N	RGD:5509061	20161117	MGI			PMID:27001178
10591	Foxg1	forkhead box G1	gene	MP:0010892	increased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
10591	Foxg1	forkhead box G1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833191
10591	Foxg1	forkhead box G1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20976199
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194867
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736290
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24327562
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7605629
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180712	MGI			PMID:27660326
10591	Foxg1	forkhead box G1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837119
10591	Foxg1	forkhead box G1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410827
10591	Foxg1	forkhead box G1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
10591	Foxg1	forkhead box G1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
10591	Foxg1	forkhead box G1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20211014	MGI			PMID:25417106
10591	Foxg1	forkhead box G1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717732
10591	Foxg1	forkhead box G1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050694
10591	Foxg1	forkhead box G1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717732
10591	Foxg1	forkhead box G1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917506
10591	Foxg1	forkhead box G1	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10591	Foxg1	forkhead box G1	gene	MP:0012559	decreased forebrain volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0012683	absent telencephalon		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10591	Foxg1	forkhead box G1	gene	MP:0013820	absent optic cup		IAGP		N	RGD:5509061	20161201	MGI			PMID:26670829
10591	Foxg1	forkhead box G1	gene	MP:0014318	abnormal oligodendrocyte differentiation		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0014516	abnormal middle ear development		IAGP		N	RGD:5509061	20240912	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0020083	decreased hippocampus volume		IAGP		N	RGD:5509061	20170706	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0020389	increased radial glial cell number		IAGP		N	RGD:5509061	20250724	MGI			PMID:40404610
10591	Foxg1	forkhead box G1	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:17640820
10591	Foxg1	forkhead box G1	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20181011	MGI			PMID:26107939
10591	Foxg1	forkhead box G1	gene	MP:0030228	absent tubotympanic recess		IAGP		N	RGD:5509061	20171019	MGI			PMID:16600992
10591	Foxg1	forkhead box G1	gene	MP:0030250	frontonasal prominence hypoplasia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
10591	Foxg1	forkhead box G1	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20171214	MGI			PMID:12717732
10591	Foxg1	forkhead box G1	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
10591	Foxg1	forkhead box G1	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:21982646
10592	Flg	filaggrin	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
10592	Flg	filaggrin	gene	MP:0000019	thick ears		IAGP		N	RGD:5509061	20171102	MGI			PMID:4557539
10592	Flg	filaggrin	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20141003	MGI			
10592	Flg	filaggrin	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
10592	Flg	filaggrin	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0001230	epidermal desquamation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
10592	Flg	filaggrin	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121144
10592	Flg	filaggrin	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
10592	Flg	filaggrin	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20181129	MGI			PMID:25902485
10592	Flg	filaggrin	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121144
10592	Flg	filaggrin	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20181129	MGI			PMID:25902485
10592	Flg	filaggrin	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
10592	Flg	filaggrin	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366455
10592	Flg	filaggrin	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0003809	abnormal hair shaft morphology		IEA		N	RGD:5509061	20141003	MGI			
10592	Flg	filaggrin	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0003846	matted coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0009598	thin epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0009605	decreased keratohyalin granule number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22409988
10592	Flg	filaggrin	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349982
10592	Flg	filaggrin	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0009795	epidermal spongiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23844115
10592	Flg	filaggrin	gene	MP:0009801	abnormal hair cortex keratinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
10592	Flg	filaggrin	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
10592	Flg	filaggrin	gene	MP:0010686	abnormal hair follicle matrix region morphology		IEA		N	RGD:5509061	20141003	MGI			
10592	Flg	filaggrin	gene	MP:0012078	abnormal tail ring morphology		IAGP		N	RGD:5509061	20170309	MGI			PMID:4557539
10592	Flg	filaggrin	gene	MP:0013178	tail necrosis		IAGP		N	RGD:5509061	20170309	MGI			PMID:4557539
10592	Flg	filaggrin	gene	MP:0020084	short ears		IAGP		N	RGD:5509061	20171102	MGI			PMID:4557539
10593	Fmo1	flavin containing monooxygenase 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20241121	MGI			
10593	Fmo1	flavin containing monooxygenase 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20240523	MGI			PMID:34500002
10593	Fmo1	flavin containing monooxygenase 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
10593	Fmo1	flavin containing monooxygenase 1	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20240523	MGI			PMID:34500002
10593	Fmo1	flavin containing monooxygenase 1	gene	MP:0014433	increased cytokine level		IAGP		N	RGD:5509061	20240523	MGI			PMID:34500002
10594	Fn1	fibronectin 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141127	MGI			PMID:21320502
10594	Fn1	fibronectin 1	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847088
10594	Fn1	fibronectin 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847088
10594	Fn1	fibronectin 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
10594	Fn1	fibronectin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847088
10594	Fn1	fibronectin 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367684
10594	Fn1	fibronectin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847088
10594	Fn1	fibronectin 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11231631
10594	Fn1	fibronectin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976060
10594	Fn1	fibronectin 1	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:11231631
10594	Fn1	fibronectin 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11231631
10594	Fn1	fibronectin 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976060
10594	Fn1	fibronectin 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141127	MGI			PMID:21320502
10594	Fn1	fibronectin 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976060
10594	Fn1	fibronectin 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976060
10594	Fn1	fibronectin 1	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11231631
10594	Fn1	fibronectin 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847088
10594	Fn1	fibronectin 1	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0010656	thick myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
10594	Fn1	fibronectin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17706958
10594	Fn1	fibronectin 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359774
10594	Fn1	fibronectin 1	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8306876
10594	Fn1	fibronectin 1	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0012277	increased tail bud apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591922
10594	Fn1	fibronectin 1	gene	MP:0013200	head mesenchyme hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8906418
10594	Fn1	fibronectin 1	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359774
10594	Fn1	fibronectin 1	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200924	MGI			PMID:12606706
10594	Fn1	fibronectin 1	gene	MP:0031593	decreased cardiac jelly amount		IAGP		N	RGD:5509061	20240229	MGI			PMID:8306876
10595	Fnta	farnesyltransferase, CAAX box, alpha	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201231	MGI			
10595	Fnta	farnesyltransferase, CAAX box, alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10595	Fnta	farnesyltransferase, CAAX box, alpha	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
10595	Fnta	farnesyltransferase, CAAX box, alpha	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
10597	Fosl1	fos-like antigen 1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15229648
10597	Fosl1	fos-like antigen 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15229648
10597	Fosl1	fos-like antigen 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15229648
10597	Fosl1	fos-like antigen 1	gene	MP:0004230	abnormal embryonic erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0004560	abnormal chorionic plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15229648
10597	Fosl1	fos-like antigen 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15229648
10597	Fosl1	fos-like antigen 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0011203	abnormal parietal yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044407
10597	Fosl1	fos-like antigen 1	gene	MP:0020515	abnormal visceral yolk sac endoderm morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:11044407
10598	Fosl2	fos-like antigen 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:18548006
10598	Fosl2	fos-like antigen 2	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607691
10598	Fosl2	fos-like antigen 2	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18548006
10598	Fosl2	fos-like antigen 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607691
10598	Fosl2	fos-like antigen 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20171221	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18548006
10598	Fosl2	fos-like antigen 2	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18548006
10598	Fosl2	fos-like antigen 2	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18548006
10598	Fosl2	fos-like antigen 2	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18548006
10598	Fosl2	fos-like antigen 2	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18548006
10598	Fosl2	fos-like antigen 2	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141016	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607691
10598	Fosl2	fos-like antigen 2	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:24046454
10598	Fosl2	fos-like antigen 2	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:15509771
10598	Fosl2	fos-like antigen 2	gene	MP:0030985	decreased circulating osteocalcin level		IAGP		N	RGD:5509061	20191219	MGI			PMID:24046454
10599	Fpgs	folylpolyglutamyl synthetase	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416011
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416011
10600	Fshb	follicle stimulating hormone beta	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416011
10600	Fshb	follicle stimulating hormone beta	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20250213	MGI			PMID:11416011
10600	Fshb	follicle stimulating hormone beta	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20161027	MGI			PMID:9020850
10600	Fshb	follicle stimulating hormone beta	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:11416011
10600	Fshb	follicle stimulating hormone beta	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11416011
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220929	MGI			
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001140	abnormal vagina epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001142	abnormal vagina orifice morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002293	long gestation period		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002661	abnormal corpus epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002678	increased follicle recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002782	abnormal testes secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003195	calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003529	enlarged clitoris		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20172968
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004849	abnormal testis size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004894	uterus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004894	uterus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004895	vagina atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004898	uterine hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005102	abnormal iris pigmentation		IEA		N	RGD:5509061	20240523	MGI			
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005131	increased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005131	increased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005133	increased luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0006361	abnormal female germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008334	increased gonadotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008337	increased thyrotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008975	delayed male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008976	delayed female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008980	decreased vagina weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008994	early vaginal opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11459817
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009016	abnormal estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009090	myometrium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009094	abnormal endometrial gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009221	uterus adenomyosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009222	increased uterus tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009233	enlarged sperm head		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009248	small caput epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009251	enlarged endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193578
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009433	polyovular ovarian follicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973687
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12135868
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0013348	adenohypophysis hyperplasia		IAGP		N	RGD:5509061	20150129	MGI			PMID:9811848
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0014270	decreased ovary secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:10803590
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:10775161
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11466221
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:14502087
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:11089565
10601	Fshr	follicle stimulating hormone receptor	gene	MP:0030826	decreased femur weight		IAGP		N	RGD:5509061	20181018	MGI			PMID:11089565
10603	Fst	follistatin	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20240523	MGI			
10603	Fst	follistatin	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24019467
10603	Fst	follistatin	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
10603	Fst	follistatin	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032047
10603	Fst	follistatin	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032047
10603	Fst	follistatin	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
10603	Fst	follistatin	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0002983	increased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976303
10603	Fst	follistatin	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24019467
10603	Fst	follistatin	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0003346	abnormal pectoral muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
10603	Fst	follistatin	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0004246	abnormal extensor digitorum longus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24019467
10603	Fst	follistatin	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0004648	decreased thoracic vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24019467
10603	Fst	follistatin	gene	MP:0004650	increased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24019467
10603	Fst	follistatin	gene	MP:0004791	absent lower incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12546816
10603	Fst	follistatin	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20260402	MGI			
10603	Fst	follistatin	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976303
10603	Fst	follistatin	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12546816
10603	Fst	follistatin	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976303
10603	Fst	follistatin	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12546816
10603	Fst	follistatin	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0008922	abnormal cervical rib		IAGP		N	RGD:5509061	20141003	MGI			PMID:24019467
10603	Fst	follistatin	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032047
10603	Fst	follistatin	gene	MP:0009361	abnormal primordial ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032047
10603	Fst	follistatin	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0009894	absent hard palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12546816
10603	Fst	follistatin	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
10603	Fst	follistatin	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10603	Fst	follistatin	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885475
10603	Fst	follistatin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
10603	Fst	follistatin	gene	MP:0011124	increased primary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:20032047
10603	Fst	follistatin	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:14701941
10603	Fst	follistatin	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:20032047
10603	Fst	follistatin	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:20032047
10603	Fst	follistatin	gene	MP:0031383	increased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:20032047
10603	Fst	follistatin	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:14701941
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757696
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751857
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751857
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751857
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751857
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751857
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0003891	increased allantois apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751857
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751857
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777375
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0012606	increased glutathione level		IAGP		N	RGD:5509061	20180111	MGI			PMID:17693254
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169625
10608	G6pdx	glucose-6-phosphate dehydrogenase X-linked	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:12169625
10610	Gabra3	gamma-aminobutyric acid type A receptor subunit alpha 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220428	MGI			
10610	Gabra3	gamma-aminobutyric acid type A receptor subunit alpha 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20111116	MGI			
10610	Gabra3	gamma-aminobutyric acid type A receptor subunit alpha 3	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284244
10610	Gabra3	gamma-aminobutyric acid type A receptor subunit alpha 3	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284244
10610	Gabra3	gamma-aminobutyric acid type A receptor subunit alpha 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:16284244
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0002679	abnormal corpus luteum morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0005134	decreased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20160204	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:24281383
10611	Gabrb1	gamma-aminobutyric acid type A receptor subunit beta 1	gene	MP:0014384	increased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:24281383
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20220421	MGI			PMID:11331371
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331371
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0004287	abnormal spiral limbus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0004490	type IV spiral ligament fibrocyte degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0004632	abnormal cochlear OHC efferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:13679430
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10612	Gabrb2	gamma-aminobutyric acid type A receptor subunit beta 2	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12475885
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117532
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001400	hyperresponsive		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20170921	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12475885
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002068	abnormal parental behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:15681950
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20170921	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12475885
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20170921	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0002911	abnormal inhibitory postsynaptic potential		IAGP		N	RGD:5509061	20170921	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0003637	cochlear ganglion hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117532
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0003986	small cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117532
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117532
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:12475885
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004490	type IV spiral ligament fibrocyte degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004632	abnormal cochlear OHC efferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004716	abnormal cochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004746	abnormal cochlear IHC afferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0005387	immune system phenotype		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12475885
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15681950
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0006409	vestibular ganglion hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117532
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20170921	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12475885
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20170921	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009957	abnormal cerebellum vermis lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009989	abnormal cerebellum vermis lobule II morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009990	abnormal cerebellum vermis lobule III morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009991	abnormal cerebellum vermis lobule IV morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009993	abnormal cerebellum vermis lobule V morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009994	abnormal cerebellum vermis lobule VI morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0009995	abnormal cerebellum vermis lobule VII morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0010232	delayed skin pigmentation appearance		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9108119
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20170921	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011273	prolonged excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20240418	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927825
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20240405	MGI			PMID:17021187
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0014486	prolonged miniature inhibitory postsynaptic current decay phase		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0014625	abnormal ictal brain wave pattern		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0020335	abnormal dentate gyrus neuron dendrite morphology		IAGP		N	RGD:5509061	20170921	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20170921	MGI			PMID:26627235
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20250828	MGI			PMID:32467926
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:17983671
10614	Gabrb3	GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:17021187
10615	Gad1	glutamate decarboxylase 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10211762
10615	Gad1	glutamate decarboxylase 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10615	Gad1	glutamate decarboxylase 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9177246
10615	Gad1	glutamate decarboxylase 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
10615	Gad1	glutamate decarboxylase 1	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17582330
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9177246
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9177246
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18384748
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18384748
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20171019	MGI			PMID:9326630
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326630
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615733
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615733
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9177246
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20171019	MGI			PMID:9326630
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9177246
10615	Gad1	glutamate decarboxylase 1	gene	MP:0001985	abnormal gustatory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625513
10615	Gad1	glutamate decarboxylase 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
10615	Gad1	glutamate decarboxylase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10211762
10615	Gad1	glutamate decarboxylase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17582330
10615	Gad1	glutamate decarboxylase 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654854
10615	Gad1	glutamate decarboxylase 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10615	Gad1	glutamate decarboxylase 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
10615	Gad1	glutamate decarboxylase 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11248119
10615	Gad1	glutamate decarboxylase 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18384748
10615	Gad1	glutamate decarboxylase 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10615	Gad1	glutamate decarboxylase 1	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10615	Gad1	glutamate decarboxylase 1	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625513
10615	Gad1	glutamate decarboxylase 1	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654854
10615	Gad1	glutamate decarboxylase 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18384748
10615	Gad1	glutamate decarboxylase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
10615	Gad1	glutamate decarboxylase 1	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17582330
10615	Gad1	glutamate decarboxylase 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
10615	Gad1	glutamate decarboxylase 1	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11248119
10615	Gad1	glutamate decarboxylase 1	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326630
10615	Gad1	glutamate decarboxylase 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376969
10615	Gad1	glutamate decarboxylase 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
10615	Gad1	glutamate decarboxylase 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
10615	Gad1	glutamate decarboxylase 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
10615	Gad1	glutamate decarboxylase 1	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326630
10615	Gad1	glutamate decarboxylase 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:9177246
10615	Gad1	glutamate decarboxylase 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
10615	Gad1	glutamate decarboxylase 1	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20333300
10615	Gad1	glutamate decarboxylase 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326630
10615	Gad1	glutamate decarboxylase 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20333300
10615	Gad1	glutamate decarboxylase 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326630
10615	Gad1	glutamate decarboxylase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615733
10615	Gad1	glutamate decarboxylase 1	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20333300
10615	Gad1	glutamate decarboxylase 1	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10615	Gad1	glutamate decarboxylase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10211762
10615	Gad1	glutamate decarboxylase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9177246
10615	Gad1	glutamate decarboxylase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326630
10615	Gad1	glutamate decarboxylase 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17582330
10615	Gad1	glutamate decarboxylase 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615733
10615	Gad1	glutamate decarboxylase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10211762
10615	Gad1	glutamate decarboxylase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376969
10615	Gad1	glutamate decarboxylase 1	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20161110	MGI			PMID:26261347
10615	Gad1	glutamate decarboxylase 1	gene	MP:0012595	decreased glutamate decarboxylase activity		IAGP		N	RGD:5509061	20180927	MGI			PMID:9177246
10615	Gad1	glutamate decarboxylase 1	gene	MP:0030248	narrow maxilla		IAGP		N	RGD:5509061	20171019	MGI			PMID:9326630
10615	Gad1	glutamate decarboxylase 1	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:10211762
10615	Gad1	glutamate decarboxylase 1	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:9177246
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10211762
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10814732
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14676944
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10814732
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20201022	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14676944
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10814732
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14676944
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8954991
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391152
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10211762
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10814732
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14676944
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391152
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:24027099
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20141003	MGI			PMID:24027099
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:24027099
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:24027099
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20170105	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10814732
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:10814732
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10814732
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160421	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14676944
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20170105	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20170105	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20211021	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418495
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10211762
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10211762
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:24027099
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24027099
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0014254	increased paired-pulse ratio		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:10211762
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:10814732
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:9391152
10616	Gad2	glutamic acid decarboxylase 2	gene	MP:0031334	increased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:39127888
10617	Galk1	galactokinase 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915771
10617	Galk1	galactokinase 1	gene	MP:0004018	abnormal galactose homeostasis		IAGP		N	RGD:5509061	20260402	MGI			PMID:10915771
10617	Galk1	galactokinase 1	gene	MP:0014932	increased galactitol level		IAGP		N	RGD:5509061	20260402	MGI			PMID:10915771
10617	Galk1	galactokinase 1	gene	MP:0014941	increased lens galactitol level		IAGP		N	RGD:5509061	20260402	MGI			PMID:10915771
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0000679	increased percent water in carcass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0001506	limp posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0010062	decreased creatine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0010065	decreased circulating creatine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0011468	abnormal urine amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0011471	decreased urine creatinine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:15028668
10618	Gamt	guanidinoacetate methyltransferase	gene	MP:0030633	decreased urine creatine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:15028668
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20221215	MGI			
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0002596	abnormal hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:17874335
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20221215	MGI			
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:17874335
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:17874335
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17874335
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:2040452
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:3796661
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960038
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17874335
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17874335
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0011609	decreased glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:17874335
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0014964	decreased circulating enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:3796661
10619	Gapdh	glyceraldehyde-3-phosphate dehydrogenase	gene	MP:0014964	decreased circulating enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:3960038
10620	Gast	gastrin	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731364
10620	Gast	gastrin	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12145805
10620	Gast	gastrin	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9287997
10620	Gast	gastrin	gene	MP:0000501	abnormal digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15735748
10620	Gast	gastrin	gene	MP:0000501	abnormal digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9530158
10620	Gast	gastrin	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15735748
10620	Gast	gastrin	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15735748
10620	Gast	gastrin	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731364
10620	Gast	gastrin	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731364
10620	Gast	gastrin	gene	MP:0003892	abnormal gastric gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11705756
10620	Gast	gastrin	gene	MP:0003892	abnormal gastric gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9530158
10620	Gast	gastrin	gene	MP:0004138	abnormal mucous neck cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9287997
10620	Gast	gastrin	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11705756
10620	Gast	gastrin	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388185
10620	Gast	gastrin	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9287997
10620	Gast	gastrin	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9530158
10620	Gast	gastrin	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9287997
10620	Gast	gastrin	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20150312	MGI			PMID:11705756
10620	Gast	gastrin	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755804
10620	Gast	gastrin	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12145805
10620	Gast	gastrin	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731364
10620	Gast	gastrin	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755804
10620	Gast	gastrin	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:9287997
10620	Gast	gastrin	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12145805
10620	Gast	gastrin	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15735748
10620	Gast	gastrin	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11705756
10620	Gast	gastrin	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15735748
10620	Gast	gastrin	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9287997
10620	Gast	gastrin	gene	MP:0011896	increased circulating unsaturated transferrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755804
10621	Gata1	GATA binding protein 1	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354171
10621	Gata1	GATA binding protein 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:12045237
10621	Gata1	GATA binding protein 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
10621	Gata1	GATA binding protein 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
10621	Gata1	GATA binding protein 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354171
10621	Gata1	GATA binding protein 1	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077323
10621	Gata1	GATA binding protein 1	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9233806
10621	Gata1	GATA binding protein 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354171
10621	Gata1	GATA binding protein 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15895080
10621	Gata1	GATA binding protein 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23717580
10621	Gata1	GATA binding protein 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15895080
10621	Gata1	GATA binding protein 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15895080
10621	Gata1	GATA binding protein 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9139715
10621	Gata1	GATA binding protein 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12045237
10621	Gata1	GATA binding protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354171
10621	Gata1	GATA binding protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9716588
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077323
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175249
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354171
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901585
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9139715
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9233806
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107690
10621	Gata1	GATA binding protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9139715
10621	Gata1	GATA binding protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:9139715
10621	Gata1	GATA binding protein 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:9139715
10621	Gata1	GATA binding protein 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10562540
10621	Gata1	GATA binding protein 1	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416124
10621	Gata1	GATA binding protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15375268
10621	Gata1	GATA binding protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12954777
10621	Gata1	GATA binding protein 1	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15375268
10621	Gata1	GATA binding protein 1	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354171
10621	Gata1	GATA binding protein 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077323
10621	Gata1	GATA binding protein 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15895080
10621	Gata1	GATA binding protein 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354171
10621	Gata1	GATA binding protein 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9233806
10621	Gata1	GATA binding protein 1	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15895080
10621	Gata1	GATA binding protein 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9233806
10621	Gata1	GATA binding protein 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0002596	abnormal hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:9233806
10621	Gata1	GATA binding protein 1	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12045237
10621	Gata1	GATA binding protein 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9233806
10621	Gata1	GATA binding protein 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0003405	abnormal platelet shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0003405	abnormal platelet shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15005853
10621	Gata1	GATA binding protein 1	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15005853
10621	Gata1	GATA binding protein 1	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12045237
10621	Gata1	GATA binding protein 1	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
10621	Gata1	GATA binding protein 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
10621	Gata1	GATA binding protein 1	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416124
10621	Gata1	GATA binding protein 1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354171
10621	Gata1	GATA binding protein 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0008247	abnormal mononuclear cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354171
10621	Gata1	GATA binding protein 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9233806
10621	Gata1	GATA binding protein 1	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
10621	Gata1	GATA binding protein 1	gene	MP:0008609	decreased circulating interleukin-13 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
10621	Gata1	GATA binding protein 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9233806
10621	Gata1	GATA binding protein 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16391009
10621	Gata1	GATA binding protein 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19682090
10621	Gata1	GATA binding protein 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23717580
10621	Gata1	GATA binding protein 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9139715
10621	Gata1	GATA binding protein 1	gene	MP:0009246	pale spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657742
10621	Gata1	GATA binding protein 1	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11342429
10621	Gata1	GATA binding protein 1	gene	MP:0009676	abnormal hemostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
10621	Gata1	GATA binding protein 1	gene	MP:0010178	increased number of Howell-Jolly bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15005853
10621	Gata1	GATA binding protein 1	gene	MP:0010964	increased compact bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15005853
10621	Gata1	GATA binding protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077323
10621	Gata1	GATA binding protein 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077323
10621	Gata1	GATA binding protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901585
10621	Gata1	GATA binding protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9139715
10621	Gata1	GATA binding protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175249
10621	Gata1	GATA binding protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077323
10621	Gata1	GATA binding protein 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966598
10621	Gata1	GATA binding protein 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260507	MGI			PMID:8901585
10621	Gata1	GATA binding protein 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:15175249
10621	Gata1	GATA binding protein 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:9139715
10621	Gata1	GATA binding protein 1	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260611	MGI			PMID:9576834
10621	Gata1	GATA binding protein 1	gene	MP:0014993	erythrocyte maturation arrest		IAGP		N	RGD:5509061	20260514	MGI			PMID:12077323
10621	Gata1	GATA binding protein 1	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:15175249
10621	Gata1	GATA binding protein 1	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:12149188
10621	Gata1	GATA binding protein 1	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:15005853
10621	Gata1	GATA binding protein 1	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20210805	MGI			PMID:14656885
10621	Gata1	GATA binding protein 1	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:15895080
10621	Gata1	GATA binding protein 1	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:9139715
10624	Gc	vitamin D binding protein	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
10624	Gc	vitamin D binding protein	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20170105	MGI			
10624	Gc	vitamin D binding protein	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916136
10624	Gc	vitamin D binding protein	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20170105	MGI			
10624	Gc	vitamin D binding protein	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916136
10624	Gc	vitamin D binding protein	gene	MP:0003432	increased activity of parathyroid		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916136
10624	Gc	vitamin D binding protein	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916136
10624	Gc	vitamin D binding protein	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
10624	Gc	vitamin D binding protein	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
10624	Gc	vitamin D binding protein	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20231207	MGI			
10624	Gc	vitamin D binding protein	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916136
10626	Gcg	glucagon	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
10626	Gcg	glucagon	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0009167	increased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819987
10626	Gcg	glucagon	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354782
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829665
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027356
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027356
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354782
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829665
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027356
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829665
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354782
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0004494	abnormal synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829665
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0004495	decreased synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829665
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829665
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354782
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354782
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829665
10630	Gdi1	GDP dissociation inhibitor 1	gene	MP:0014744	abnormal hippocampal mossy fiber suprapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:12354782
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537792
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439720
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:24656820
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574104
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24656820
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15130495
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536709
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19954518
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001011	abnormal superior cervical ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11774071
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001047	abnormal enteric cholinergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372284
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600854
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372284
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536709
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537792
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536709
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574104
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:11774071
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002827	abnormal renal corpuscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11422733
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002827	abnormal renal corpuscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574104
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002955	increased compensatory renal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11422733
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537792
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:24656820
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003268	chronic constipation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11774071
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11774071
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003307	pyloric stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003437	abnormal carotid body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536709
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439720
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11422733
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11774071
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536709
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11422733
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536709
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0004103	abnormal ventral striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536709
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11422733
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574104
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24656820
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574104
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11422733
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0006100	abnormal tegmentum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536709
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0009511	distended stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:11774071
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0009684	abnormal spinal cord lateral motor column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372284
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0010800	abnormal submucous nerve plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11774071
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0010801	abnormal myenteric nerve plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11774071
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657307
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657308
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11774071
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11422733
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574104
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574104
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011359	decreased glomerular capillary number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574104
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943767
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0011881	distended duodenum		IAGP		N	RGD:5509061	20150702	MGI			PMID:8657306
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:19954518
10631	Gdnf	glial cell line derived neurotrophic factor	gene	MP:0020491	abnormal ovary topology		IAGP		N	RGD:5509061	20171026	MGI			PMID:8657308
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252036
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116877
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252036
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116877
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393124
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116877
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116877
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20191212	MGI			PMID:29961578
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116877
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252036
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201217	MGI			PMID:31077553
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002620	abnormal monocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116877
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004327	increased vestibular hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20191212	MGI			PMID:29961578
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004403	absent cochlear outer hair cells		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004465	degeneration of organ of Corti supporting cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004530	absent outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004536	short inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004589	abnormal cochlear hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004632	abnormal cochlear OHC efferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826720
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116877
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116877
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116877
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393124
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0008112	abnormal monocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:11810106
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0008791	decreased NK cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393124
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932805
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393124
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0011061	abnormal inner hair cell kinocilium morphology		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20191219	MGI			PMID:31444330
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0011689	absent neutrophils		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393124
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397623
10634	Gfi1	growth factor independent 1 transcription repressor	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20063299
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507417
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000392	accelerated hair follicle regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702420
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10682708
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10682708
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10682708
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541311
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507417
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23542432
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728913
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10682708
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10682708
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728913
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541311
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19954518
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19954518
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372284
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19954518
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001033	abnormal parasympathetic system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069590
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10682708
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507417
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728913
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507417
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728913
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541311
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507417
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372284
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372284
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001085	small petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001087	abnormal nodose ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702420
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0001664	abnormal digestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10682708
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728913
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541311
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23542432
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:17507417
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003585	large ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:23542432
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23542432
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541311
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:10682708
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003827	abnormal Wolffian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507417
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541311
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507417
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23542432
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728913
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322904
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0008314	abnormal pterygopalatine ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069590
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0008315	abnormal otic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069590
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0009684	abnormal spinal cord lateral motor column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372284
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0010981	abnormal branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23542432
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728913
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10682708
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507417
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728913
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541311
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0011292	absent nephron		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697851
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0011760	abnormal ureteric bud tip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23542432
10635	Gfra1	glial cell line derived neurotrophic factor family receptor alpha 1	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:19954518
10636	Ggh	gamma-glutamyl hydrolase	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
10636	Ggh	gamma-glutamyl hydrolase	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20220519	MGI			
10636	Ggh	gamma-glutamyl hydrolase	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900463
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002293	long gestation period		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374408
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20190613	MGI			PMID:17255313
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374408
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20190613	MGI			PMID:17255313
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002768	small adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20190613	MGI			PMID:17255313
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039218
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039218
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039218
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900463
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0004514	dystocia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374408
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374408
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20190613	MGI			PMID:17255313
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20190613	MGI			PMID:17255313
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20190613	MGI			PMID:17255313
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005410	abnormal fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374408
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900463
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374408
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714507
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900463
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0008294	abnormal adrenal gland zona fasciculata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0008295	abnormal adrenal gland zona reticularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039218
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9155011
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374408
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20190613	MGI			PMID:17255313
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20190613	MGI			PMID:17255313
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0013337	abnormal adenohypophysis development		IAGP		N	RGD:5509061	20141211	MGI			PMID:9013935
10640	B4galt1	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	gene	MP:0020180	abnormal IgM level		IAGP		N	RGD:5509061	20190613	MGI			PMID:17255313
10643	Gh	growth hormone	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
10643	Gh	growth hormone	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20170105	MGI			
10643	Gh	growth hormone	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20170105	MGI			
10643	Gh	growth hormone	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20170105	MGI			
10643	Gh	growth hormone	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210520	MGI			
10643	Gh	growth hormone	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20190530	MGI			
10643	Gh	growth hormone	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
10643	Gh	growth hormone	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
10643	Gh	growth hormone	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
10643	Gh	growth hormone	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20170105	MGI			
10643	Gh	growth hormone	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20170105	MGI			
10643	Gh	growth hormone	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20201022	MGI			
10643	Gh	growth hormone	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20170105	MGI			
10643	Gh	growth hormone	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20231207	MGI			
10643	Gh	growth hormone	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20231207	MGI			
10643	Gh	growth hormone	gene	MP:0003918	decreased kidney weight		IEA		N	RGD:5509061	20210128	MGI			
10643	Gh	growth hormone	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
10643	Gh	growth hormone	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20210128	MGI			
10643	Gh	growth hormone	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20160421	MGI			
10643	Gh	growth hormone	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141127	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0008330	absent somatotrophs		IAGP		N	RGD:5509061	20141127	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0008333	absent lactotrophs		IAGP		N	RGD:5509061	20141127	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0008938	decreased pituitary gland weight		IAGP		N	RGD:5509061	20141127	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
10643	Gh	growth hormone	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
10643	Gh	growth hormone	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160811	MGI			
10643	Gh	growth hormone	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
10643	Gh	growth hormone	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10643	Gh	growth hormone	gene	MP:0011612	increased circulating ghrelin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726450
10643	Gh	growth hormone	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
10644	Ghr	growth hormone receptor	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231300
10644	Ghr	growth hormone receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601831
10644	Ghr	growth hormone receptor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875265
10644	Ghr	growth hormone receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875265
10644	Ghr	growth hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10974652
10644	Ghr	growth hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231300
10644	Ghr	growth hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884384
10644	Ghr	growth hormone receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875265
10644	Ghr	growth hormone receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
10644	Ghr	growth hormone receptor	gene	MP:0001462	abnormal avoidance learning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11336996
10644	Ghr	growth hormone receptor	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601831
10644	Ghr	growth hormone receptor	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875265
10644	Ghr	growth hormone receptor	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875265
10644	Ghr	growth hormone receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601831
10644	Ghr	growth hormone receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11395925
10644	Ghr	growth hormone receptor	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0001784	abnormal fluid regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20240613	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11336996
10644	Ghr	growth hormone receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231300
10644	Ghr	growth hormone receptor	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601831
10644	Ghr	growth hormone receptor	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884384
10644	Ghr	growth hormone receptor	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19269870
10644	Ghr	growth hormone receptor	gene	MP:0002293	long gestation period		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10974652
10644	Ghr	growth hormone receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11395925
10644	Ghr	growth hormone receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0002782	abnormal testes secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19269870
10644	Ghr	growth hormone receptor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10974652
10644	Ghr	growth hormone receptor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0002965	increased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601831
10644	Ghr	growth hormone receptor	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555853
10644	Ghr	growth hormone receptor	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0003356	impaired luteinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601831
10644	Ghr	growth hormone receptor	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884384
10644	Ghr	growth hormone receptor	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11395925
10644	Ghr	growth hormone receptor	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231300
10644	Ghr	growth hormone receptor	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884384
10644	Ghr	growth hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875265
10644	Ghr	growth hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601831
10644	Ghr	growth hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884384
10644	Ghr	growth hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10614635
10644	Ghr	growth hormone receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0004908	abnormal seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0004927	abnormal epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884384
10644	Ghr	growth hormone receptor	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231300
10644	Ghr	growth hormone receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884384
10644	Ghr	growth hormone receptor	gene	MP:0005473	decreased triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11395925
10644	Ghr	growth hormone receptor	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11395925
10644	Ghr	growth hormone receptor	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:11395925
10644	Ghr	growth hormone receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555853
10644	Ghr	growth hormone receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11395925
10644	Ghr	growth hormone receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20240523	MGI			
10644	Ghr	growth hormone receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19269870
10644	Ghr	growth hormone receptor	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0008938	decreased pituitary gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0008940	delayed balanopreputial separation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10644	Ghr	growth hormone receptor	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0008975	delayed male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0008976	delayed female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0009019	abnormal metestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297526
10644	Ghr	growth hormone receptor	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555853
10644	Ghr	growth hormone receptor	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20200402	MGI			PMID:31806625
10644	Ghr	growth hormone receptor	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0009286	increased abdominal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601831
10644	Ghr	growth hormone receptor	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884384
10644	Ghr	growth hormone receptor	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884384
10644	Ghr	growth hormone receptor	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231300
10644	Ghr	growth hormone receptor	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460757
10644	Ghr	growth hormone receptor	gene	MP:0009425	increased soleus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601831
10644	Ghr	growth hormone receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20200402	MGI			PMID:31806625
10644	Ghr	growth hormone receptor	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371826
10644	Ghr	growth hormone receptor	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20150611	MGI			PMID:21555853
10644	Ghr	growth hormone receptor	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31806625
10644	Ghr	growth hormone receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174655
10644	Ghr	growth hormone receptor	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20250410	MGI			PMID:10974652
10644	Ghr	growth hormone receptor	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20150319	MGI			PMID:10631109
10644	Ghr	growth hormone receptor	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:10067829
10644	Ghr	growth hormone receptor	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:12185100
10644	Ghr	growth hormone receptor	gene	MP:0014810	increased circulating urea level		IAGP		N	RGD:5509061	20251204	MGI			PMID:15138153
10644	Ghr	growth hormone receptor	gene	MP:0015006	decreased fetal length		IAGP		N	RGD:5509061	20260611	MGI			PMID:10342852
10644	Ghr	growth hormone receptor	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:23349524
10644	Ghr	growth hormone receptor	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:15231300
10644	Ghr	growth hormone receptor	gene	MP:0031362	decreased prostate gland ventral lobe weight		IAGP		N	RGD:5509061	20220303	MGI			PMID:10067829
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20160421	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12537301
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18063435
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388430
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210520	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12537301
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:978118
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1270792
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1270792
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1270792
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:978118
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20160421	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20170105	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210520	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0003194	abnormal frequency of paradoxical sleep		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388430
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:1270792
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20141003	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:12537301
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18063435
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960295
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7679139
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1270792
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1270792
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12537301
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:1270792
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:18063435
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008156	decreased diameter of tibia		IAGP		N	RGD:5509061	20220922	MGI			PMID:18063435
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008322	abnormal somatotroph morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6194978
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008329	decreased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6194978
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008417	decreased somatotroph cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:6194978
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008436	decreased somatotroph secretory granule number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6194978
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008437	absent somatotroph secretory granules		IAGP		N	RGD:5509061	20141003	MGI			PMID:6194978
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008831	abnormal insulin-like growth factor I level		IEA		N	RGD:5509061	20141003	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:978118
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:7679139
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0010119	abnormal bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0013615	increased volumetric bone mineral density		IAGP		N	RGD:5509061	20220922	MGI			PMID:18063435
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0013616	decreased volumetric bone mineral density		IEA		N	RGD:5509061	20150319	MGI			
10645	Ghrhr	growth hormone releasing hormone receptor	gene	MP:0020010	decreased bone mineral density of femur		IEA		N	RGD:5509061	20141003	MGI			
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000126	brittle teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118799
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17644066
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118799
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000448	pointed snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077386
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601660
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259389
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208994
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208994
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220407	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208994
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109444
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481448
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109444
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7892609
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481448
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001629	abnormal heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21527737
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:7892609
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259389
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259389
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259389
10649	Gja1	gap junction protein, alpha 1	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:7892609
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118799
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11179202
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118799
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135457
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481448
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16703618
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:22135478
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208994
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002336	abnormal pulmonary gas exchange		IAGP		N	RGD:5509061	20141003	MGI			PMID:7892609
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038639
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11179202
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:14967725
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259389
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002748	abnormal pulmonary valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7892609
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002776	increased Sertoli cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12840073
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21527737
10649	Gja1	gap junction protein, alpha 1	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003108	short zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14967725
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077386
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21527737
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109444
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003356	impaired luteinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003390	lymphedema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18958191
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20250508	MGI			
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003838	abnormal milk ejection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0003930	abnormal tooth hard tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7892609
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16802337
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004116	abnormal atrioventricular bundle conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077386
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004225	patent cardiac foramen ovale		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20171026	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20170914	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141009	MGI			PMID:22652908
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514348
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481448
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481448
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141009	MGI			PMID:22652908
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006049	semilunar valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006097	abnormal cerebellar lobule formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006110	ventricular fibrillation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7892609
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481448
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259389
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077386
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20260514	MGI			PMID:17038639
10649	Gja1	gap junction protein, alpha 1	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481448
10649	Gja1	gap junction protein, alpha 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20260514	MGI			PMID:14967725
10649	Gja1	gap junction protein, alpha 1	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20260514	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010194	absent lymphatic vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109444
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010394	decreased QRS amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010394	decreased QRS amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077386
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010428	abnormal heart right ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010428	abnormal heart right ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010428	abnormal heart right ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7892609
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010449	heart right ventricle outflow tract stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010453	abnormal coronary vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010472	abnormal ascending aorta and coronary artery attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010476	coronary fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010477	coronary artery aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077386
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0010961	increased compact bone mass		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282340
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135457
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7892609
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17644066
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449318
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077386
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077386
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20250508	MGI			
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20250508	MGI			
10649	Gja1	gap junction protein, alpha 1	gene	MP:0011919	abnormal R wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20200130	MGI			PMID:19259389
10649	Gja1	gap junction protein, alpha 1	gene	MP:0013623	increased femur compact bone thickness		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0013781	abnormal mammary gland luminal epithelium morphology		IAGP		N	RGD:5509061	20150625	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0014610	increased bone marrow cavity size		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:17591950
10649	Gja1	gap junction protein, alpha 1	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0015049	disorganized cerebellar granule layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:17311295
10649	Gja1	gap junction protein, alpha 1	gene	MP:0021160	decreased heart right ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:16624854
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030034	depressed nasal bridge		IAGP		N	RGD:5509061	20170914	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030064	small face		IAGP		N	RGD:5509061	20170921	MGI			PMID:18003637
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030080	small lower incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030190	small snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030222	hyperostosis		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030278	thick neurocranium		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030281	thin parietal bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030310	abnormal cranial foramen morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030315	small neurocranium		IAGP		N	RGD:5509061	20171109	MGI			PMID:11076975
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030417	craniofacial hyperostosis		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030438	increased osteoblast proliferation		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030487	abnormal osteocyte dendritic process morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0030791	club-shaped femur		IAGP		N	RGD:5509061	20260618	MGI			PMID:39848944
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031018	decreased granulosa cell proliferation		IAGP		N	RGD:5509061	20200130	MGI			PMID:19259389
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:19259389
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031508	abnormal vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:22652908
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031526	thin right ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031584	thick semilunar valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:15548583
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031634	decreased heart right ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:16155213
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031710	polymorphic ventricular tachycardia		IAGP		N	RGD:5509061	20260618	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031710	polymorphic ventricular tachycardia		IAGP		N	RGD:5509061	20260618	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031711	monomorphic ventricular tachycardia		IAGP		N	RGD:5509061	20260618	MGI			PMID:23558439
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031718	shortened corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:17408477
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031738	atrioventricular dissociation		IAGP		N	RGD:5509061	20260716	MGI			PMID:10996788
10649	Gja1	gap junction protein, alpha 1	gene	MP:0031738	atrioventricular dissociation		IAGP		N	RGD:5509061	20260716	MGI			PMID:16155213
10650	Gla	galactosidase, alpha	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9122231
10650	Gla	galactosidase, alpha	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9122231
10650	Gla	galactosidase, alpha	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574107
10650	Gla	galactosidase, alpha	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9122231
10650	Gla	galactosidase, alpha	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574107
10650	Gla	galactosidase, alpha	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574107
10650	Gla	galactosidase, alpha	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574107
10650	Gla	galactosidase, alpha	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574107
10650	Gla	galactosidase, alpha	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574107
10650	Gla	galactosidase, alpha	gene	MP:0010506	prolonged RR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574107
10650	Gla	galactosidase, alpha	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574107
10650	Gla	galactosidase, alpha	gene	MP:0011556	increased urine beta2-microglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094090
10650	Gla	galactosidase, alpha	gene	MP:0031730	atrial premature beat		IAGP		N	RGD:5509061	20260618	MGI			PMID:22574107
10651	Glb1	galactosidase, beta 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578847
10651	Glb1	galactosidase, beta 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9063740
10651	Glb1	galactosidase, beta 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687347
10651	Glb1	galactosidase, beta 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578847
10651	Glb1	galactosidase, beta 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9063740
10651	Glb1	galactosidase, beta 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9063740
10651	Glb1	galactosidase, beta 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9063740
10651	Glb1	galactosidase, beta 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9071485
10651	Glb1	galactosidase, beta 1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578847
10651	Glb1	galactosidase, beta 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578847
10651	Glb1	galactosidase, beta 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9063740
10651	Glb1	galactosidase, beta 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9071485
10651	Glb1	galactosidase, beta 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9337086
10651	Glb1	galactosidase, beta 1	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687347
10651	Glb1	galactosidase, beta 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578847
10651	Glb1	galactosidase, beta 1	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10651	Glb1	galactosidase, beta 1	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578847
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805773
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118286
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226398
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805773
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805773
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805773
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805773
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805773
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226398
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805773
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805773
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0004167	abnormal cingulate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23671099
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226398
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118286
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805773
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464988
10652	Gclc	glutamate-cysteine ligase, catalytic subunit	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:10805773
10653	Glo1	glyoxalase 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20190314	MGI			PMID:28623132
10653	Glo1	glyoxalase 1	gene	MP:0001559	hyperglycemia		IEA		N	RGD:5509061	20160428	MGI			
10653	Glo1	glyoxalase 1	gene	MP:0002727	decreased circulating insulin level		IEA		N	RGD:5509061	20160428	MGI			
10653	Glo1	glyoxalase 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20190314	MGI			PMID:28623132
10653	Glo1	glyoxalase 1	gene	MP:0014414	increased depression-related behavior		IAGP		N	RGD:5509061	20241226	MGI			PMID:28623132
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434938
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959939
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434938
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966573
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966573
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434938
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898756
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434938
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434938
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959939
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966573
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959939
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898756
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434938
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966573
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23403053
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434938
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898756
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434938
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434938
10655	Glp1r	glucagon-like peptide 1 receptor	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920294
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847326
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23954789
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23954789
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
10656	Glra2	glycine receptor, alpha 2 subunit	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076688
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651857
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001386	abnormal maternal nurturing		IEA		N	RGD:5509061	20111116	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001407	short stride length		IEA		N	RGD:5509061	20111116	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8733750
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001504	abnormal posture		IEA		N	RGD:5509061	20111116	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651857
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001522	impaired swimming		IEA		N	RGD:5509061	20111116	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651857
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651857
10657	Glrb	glycine receptor, beta subunit	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20111116	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0004143	muscle hypertonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651857
10657	Glrb	glycine receptor, beta subunit	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076688
10657	Glrb	glycine receptor, beta subunit	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0005604	hyperekplexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651857
10657	Glrb	glycine receptor, beta subunit	gene	MP:0005604	hyperekplexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8733750
10657	Glrb	glycine receptor, beta subunit	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0009025	abnormal brain dura mater morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4323808
10657	Glrb	glycine receptor, beta subunit	gene	MP:0011086	postnatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
10657	Glrb	glycine receptor, beta subunit	gene	MP:0020422	decreased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
10659	Gls	glutaminase	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
10659	Gls	glutaminase	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:28427419
10659	Gls	glutaminase	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16641247
10659	Gls	glutaminase	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20160804	MGI			PMID:26778975
10659	Gls	glutaminase	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16641247
10659	Gls	glutaminase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16641247
10659	Gls	glutaminase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10659	Gls	glutaminase	gene	MP:0030586	impaired behavioral response to amphetamine		IAGP		N	RGD:5509061	20180614	MGI			PMID:26778975
10665	Glycam1	glycosylation dependent cell adhesion molecule 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
10665	Glycam1	glycosylation dependent cell adhesion molecule 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
10665	Glycam1	glycosylation dependent cell adhesion molecule 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
10665	Glycam1	glycosylation dependent cell adhesion molecule 1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
10669	Gnas	GNAS complex locus	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273687
10669	Gnas	GNAS complex locus	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20170202	MGI			PMID:26671181
10669	Gnas	GNAS complex locus	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15811946
10669	Gnas	GNAS complex locus	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:21747923
10669	Gnas	GNAS complex locus	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136628
10669	Gnas	GNAS complex locus	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:21747923
10669	Gnas	GNAS complex locus	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798190
10669	Gnas	GNAS complex locus	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798190
10669	Gnas	GNAS complex locus	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438605
10669	Gnas	GNAS complex locus	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273687
10669	Gnas	GNAS complex locus	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273687
10669	Gnas	GNAS complex locus	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16462745
10669	Gnas	GNAS complex locus	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274197
10669	Gnas	GNAS complex locus	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26671181
10669	Gnas	GNAS complex locus	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16822937
10669	Gnas	GNAS complex locus	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273687
10669	Gnas	GNAS complex locus	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16822937
10669	Gnas	GNAS complex locus	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274197
10669	Gnas	GNAS complex locus	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273687
10669	Gnas	GNAS complex locus	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274197
10669	Gnas	GNAS complex locus	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273687
10669	Gnas	GNAS complex locus	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20170202	MGI			PMID:26671181
10669	Gnas	GNAS complex locus	gene	MP:0002905	decreased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15811946
10669	Gnas	GNAS complex locus	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444578
10669	Gnas	GNAS complex locus	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16822937
10669	Gnas	GNAS complex locus	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0003121	genetic imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:15811946
10669	Gnas	GNAS complex locus	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798190
10669	Gnas	GNAS complex locus	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136628
10669	Gnas	GNAS complex locus	gene	MP:0003353	decreased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16822937
10669	Gnas	GNAS complex locus	gene	MP:0003416	premature bone ossification		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0003497	insensitivity to parathyroid hormone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0003546	decreased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438605
10669	Gnas	GNAS complex locus	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:15811946
10669	Gnas	GNAS complex locus	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0003705	abnormal hypodermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21747923
10669	Gnas	GNAS complex locus	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136628
10669	Gnas	GNAS complex locus	gene	MP:0003948	abnormal gas homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0003948	abnormal gas homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16822937
10669	Gnas	GNAS complex locus	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0004913	absent mandibular angle		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274197
10669	Gnas	GNAS complex locus	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136628
10669	Gnas	GNAS complex locus	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0005406	abnormal heart size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273687
10669	Gnas	GNAS complex locus	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16822937
10669	Gnas	GNAS complex locus	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274197
10669	Gnas	GNAS complex locus	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0005581	abnormal renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16822937
10669	Gnas	GNAS complex locus	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21455290
10669	Gnas	GNAS complex locus	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0009303	decreased renal fat pad weight		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274197
10669	Gnas	GNAS complex locus	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20170202	MGI			PMID:26671181
10669	Gnas	GNAS complex locus	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20170202	MGI			PMID:26671181
10669	Gnas	GNAS complex locus	gene	MP:0009673	increased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0009702	increased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273687
10669	Gnas	GNAS complex locus	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0009892	palate bone hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0009917	abnormal hyoid bone body morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20160714	MGI			PMID:21220306
10669	Gnas	GNAS complex locus	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:16239968
10669	Gnas	GNAS complex locus	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15273686
10669	Gnas	GNAS complex locus	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883378
10669	Gnas	GNAS complex locus	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136628
10669	Gnas	GNAS complex locus	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15765186
10669	Gnas	GNAS complex locus	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22253771
10669	Gnas	GNAS complex locus	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11001929
10669	Gnas	GNAS complex locus	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0011478	abnormal urine catecholamine level		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0011563	increased urine prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16822937
10669	Gnas	GNAS complex locus	gene	MP:0011612	increased circulating ghrelin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22253771
10669	Gnas	GNAS complex locus	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215617
10669	Gnas	GNAS complex locus	gene	MP:0012336	decreased vitamin D level		IAGP		N	RGD:5509061	20170202	MGI			PMID:26671181
10669	Gnas	GNAS complex locus	gene	MP:0013585	thymus cortex atrophy		IAGP		N	RGD:5509061	20150319	MGI			PMID:9671744
10669	Gnas	GNAS complex locus	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0014167	ectopic bone		IAGP		N	RGD:5509061	20160407	MGI			PMID:21747923
10669	Gnas	GNAS complex locus	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20171228	MGI			PMID:20374964
10669	Gnas	GNAS complex locus	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:11438605
10669	Gnas	GNAS complex locus	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0030021	increased muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:11274197
10669	Gnas	GNAS complex locus	gene	MP:0030072	round face		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0030200	abnormal nasal septum cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0030367	premature metopic suture closure		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
10669	Gnas	GNAS complex locus	gene	MP:0030768	increased urine dopamine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0030772	increased urine noradrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0030773	decreased urine noradrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:10712433
10669	Gnas	GNAS complex locus	gene	MP:0031414	decreased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:20374964
10671	Gnmt	glycine N-methyltransferase	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19035462
10671	Gnmt	glycine N-methyltransferase	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160310	MGI			PMID:19035462
10671	Gnmt	glycine N-methyltransferase	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19035462
10671	Gnmt	glycine N-methyltransferase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19035462
10671	Gnmt	glycine N-methyltransferase	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16779654
10671	Gnmt	glycine N-methyltransferase	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20200910	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20160310	MGI			PMID:17937387
10671	Gnmt	glycine N-methyltransferase	gene	MP:0030644	increased circulating methionine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:17937387
10675	Got1	glutamic-oxaloacetic transaminase 1, soluble	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
10675	Got1	glutamic-oxaloacetic transaminase 1, soluble	gene	MP:0002607	decreased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
10675	Got1	glutamic-oxaloacetic transaminase 1, soluble	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
10675	Got1	glutamic-oxaloacetic transaminase 1, soluble	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
10675	Got1	glutamic-oxaloacetic transaminase 1, soluble	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20221215	MGI			
10675	Got1	glutamic-oxaloacetic transaminase 1, soluble	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10675	Got1	glutamic-oxaloacetic transaminase 1, soluble	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
10676	Gp5	glycoprotein 5 platelet	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10590056
10676	Gp5	glycoprotein 5 platelet	gene	MP:0005607	decreased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:10557321
10677	Gpc3	glypican 3	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733558
10677	Gpc3	glypican 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0001123	dilated uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0001699	increased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
10677	Gpc3	glypican 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0001867	rhinitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20150924	MGI			PMID:23327927
10677	Gpc3	glypican 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0002707	abnormal kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180950
10677	Gpc3	glypican 3	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733558
10677	Gpc3	glypican 3	gene	MP:0003315	abnormal perineum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180950
10677	Gpc3	glypican 3	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
10677	Gpc3	glypican 3	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11180950
10677	Gpc3	glypican 3	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20150924	MGI			PMID:23327927
10677	Gpc3	glypican 3	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936336
10677	Gpc3	glypican 3	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936336
10677	Gpc3	glypican 3	gene	MP:0009728	abnormal calcaneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733558
10677	Gpc3	glypican 3	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733558
10677	Gpc3	glypican 3	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733558
10677	Gpc3	glypican 3	gene	MP:0010419	inlet ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733558
10677	Gpc3	glypican 3	gene	MP:0010476	coronary fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733558
10677	Gpc3	glypican 3	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733558
10677	Gpc3	glypican 3	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733558
10677	Gpc3	glypican 3	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20150924	MGI			PMID:23327927
10677	Gpc3	glypican 3	gene	MP:0010981	abnormal branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402475
10677	Gpc3	glypican 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
10677	Gpc3	glypican 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964473
10677	Gpc3	glypican 3	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0011308	kidney corticomedullary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0011423	kidney cortex atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0011520	increased placental labyrinth size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10677	Gpc3	glypican 3	gene	MP:0014347	increased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:11846487
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12644183
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:1582174
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8408535
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2344351
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2381920
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2381920
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8408535
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:162283
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0014964	decreased circulating enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:8417789
10680	Gpi1	glucose-6-phosphate isomerase 1	gene	MP:0031084	decreased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:8417789
10681	Gpx1	glutathione peroxidase 1	gene	MP:0000316	cellular necrosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:14732290
10681	Gpx1	glutathione peroxidase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:14732290
10681	Gpx1	glutathione peroxidase 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:14732290
10681	Gpx1	glutathione peroxidase 1	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20180719	MGI			
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20180719	MGI			
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20211021	MGI			
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:10754271
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20180719	MGI			PMID:18760274
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180719	MGI			PMID:24075852
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10754271
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:12429206
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20180719	MGI			PMID:24075852
10681	Gpx1	glutathione peroxidase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20180719	MGI			
10681	Gpx1	glutathione peroxidase 1	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20180719	MGI			PMID:11545230
10681	Gpx1	glutathione peroxidase 1	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20180719	MGI			PMID:11579147
10681	Gpx1	glutathione peroxidase 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20180719	MGI			PMID:14732290
10681	Gpx1	glutathione peroxidase 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11579147
10681	Gpx1	glutathione peroxidase 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:12429206
10681	Gpx1	glutathione peroxidase 1	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:10915653
10681	Gpx1	glutathione peroxidase 1	gene	MP:0003288	intestinal edema		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20180719	MGI			PMID:11579147
10681	Gpx1	glutathione peroxidase 1	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20180719	MGI			PMID:11545230
10681	Gpx1	glutathione peroxidase 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20180719	MGI			PMID:11545230
10681	Gpx1	glutathione peroxidase 1	gene	MP:0004597	increased susceptibility to noise-induced hearing loss		IAGP		N	RGD:5509061	20180719	MGI			PMID:11545230
10681	Gpx1	glutathione peroxidase 1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20180719	MGI			
10681	Gpx1	glutathione peroxidase 1	gene	MP:0005035	perianal ulcer		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20180719	MGI			PMID:12429206
10681	Gpx1	glutathione peroxidase 1	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9195979
10681	Gpx1	glutathione peroxidase 1	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:11518697
10681	Gpx1	glutathione peroxidase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:8759521
10681	Gpx1	glutathione peroxidase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10754271
10681	Gpx1	glutathione peroxidase 1	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20180719	MGI			PMID:11579147
10681	Gpx1	glutathione peroxidase 1	gene	MP:0006080	brain ischemia		IAGP		N	RGD:5509061	20180719	MGI			PMID:11579147
10681	Gpx1	glutathione peroxidase 1	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20180719	MGI			PMID:14732290
10681	Gpx1	glutathione peroxidase 1	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20180719	MGI			PMID:14732290
10681	Gpx1	glutathione peroxidase 1	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20180719	MGI			PMID:9712879
10681	Gpx1	glutathione peroxidase 1	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:24075852
10681	Gpx1	glutathione peroxidase 1	gene	MP:0011592	abnormal catalase activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:8759521
10681	Gpx1	glutathione peroxidase 1	gene	MP:0011603	decreased glutathione peroxidase activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:20015939
10681	Gpx1	glutathione peroxidase 1	gene	MP:0011603	decreased glutathione peroxidase activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:8759521
10681	Gpx1	glutathione peroxidase 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20180719	MGI			PMID:11545230
10681	Gpx1	glutathione peroxidase 1	gene	MP:0013481	abnormal ileum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10915653
10681	Gpx1	glutathione peroxidase 1	gene	MP:0013483	abnormal jejunum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10915653
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726645
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726645
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726645
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778510
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778510
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726645
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778510
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200514	MGI			
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726645
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
10683	Grik4	glutamate receptor, ionotropic, kainate 4	gene	MP:0015051	abnormal postsynapse morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:19726645
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20210520	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210520	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20111116	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20111116	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210520	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533602
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IEA		N	RGD:5509061	20111116	MGI			
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533602
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778510
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778510
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778510
10684	Grik5	glutamate receptor, ionotropic, kainate 5 (gamma 2)	gene	MP:0011274	short excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533602
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0000860	abnormal primary somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498788
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0000862	absent barrels in primary somatosensory cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0000862	absent barrels in primary somatosensory cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498788
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12657691
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8060614
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8060614
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8060614
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776282
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345915
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244696
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313466
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12657691
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345915
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345915
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22419158
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001435	absent suckling reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313466
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8713451
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700255
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001460	abnormal olfactory discrimination memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700255
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11073458
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040087
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8980238
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9054942
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700255
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11073458
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15003177
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040087
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015831
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776282
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8980238
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265649
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12657691
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8060614
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313466
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8713451
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015831
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556551
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:11073458
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:15003177
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099814
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8060614
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313466
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8980238
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277569
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001909	reduced NMDA receptor mediated synaptic activity in barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12657691
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313466
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11073458
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16101757
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22419158
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277569
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17313573
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12657691
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776282
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002802	abnormal discrimination learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556551
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015831
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16101757
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244696
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002885	abnormal AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701074
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701074
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776282
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8060614
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8713451
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040087
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015831
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701074
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277569
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244696
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015831
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8980238
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002969	impaired social transmission of food preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700255
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20160804	MGI			
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040087
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244696
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0003546	decreased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244696
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265649
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0004000	impaired passive avoidance behavior		IEA		N	RGD:5509061	20111116	MGI			
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776282
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277569
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345915
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142228
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12657691
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313466
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0005572	abnormal pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0006335	abnormal hearing electrophysiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8713451
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:17313573
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0008462	abnormal medium spiny neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015831
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345915
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265649
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776282
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009326	absent maternal crouching		IAGP		N	RGD:5509061	20220519	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009327	abnormal maternal grooming		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:8060614
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:8713451
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345915
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701074
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776282
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10818139
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244696
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345915
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12657691
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8313466
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8713451
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8060614
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345915
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277569
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0014274	decreased respiration		IAGP		N	RGD:5509061	20230810	MGI			PMID:10729336
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0014373	increased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:18701073
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0014375	increased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:18701073
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0020157	abnormal behavioral response to alcohol		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244696
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20181220	MGI			PMID:22726567
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0021117	abnormal huddling behavior		IAGP		N	RGD:5509061	20220519	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:10481908
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:19915563
10685	Grin1	glutamate receptor, ionotropic, NMDA1 (zeta 1)	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22726567
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23201971
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20161229	MGI			PMID:27317637
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001401	jumpy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7816096
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23201971
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9458051
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20161229	MGI			PMID:27317637
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:7816096
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23201971
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7816096
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9458051
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11488959
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001500	decreased kindling response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9458051
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15317856
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987814
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19834457
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:7816096
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725314
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987814
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19834457
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725314
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987814
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0003177	allodynia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725314
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19834457
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725314
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987814
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20161229	MGI			PMID:27317637
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0008532	decreased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725314
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23201971
10686	Grin2a	glutamate receptor, ionotropic, NMDA2A (epsilon 1)	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9458051
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210826	MGI			
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0000861	disorganized barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789948
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23201971
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20231207	MGI			
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23201971
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001435	absent suckling reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789948
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710293
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001468	abnormal temporal memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234183
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726645
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234183
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23201971
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11488959
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768843
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789948
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16710293
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726645
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0001901	absence of NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789948
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768843
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002802	abnormal discrimination learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23201971
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002885	abnormal AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870468
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:9458051
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20251204	MGI			PMID:34433031
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768843
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23201971
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20230413	MGI			PMID:34433031
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20230413	MGI			PMID:34433031
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726645
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11488959
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726645
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789948
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768843
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789948
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9458051
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19081379
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210805	MGI			
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0011274	short excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20240418	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:16710293
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0015051	abnormal postsynapse morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:19726645
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20230413	MGI			PMID:34433031
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20211014	MGI			PMID:20357110
10687	Grin2b	glutamate receptor, ionotropic, NMDA2B (epsilon 2)	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22153375
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15519237
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15519237
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15519237
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9458051
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15317856
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987814
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9458051
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15317856
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17276696
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:8756432
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987814
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8756432
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987814
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987814
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15519237
10688	Grin2c	glutamate receptor, ionotropic, NMDA2C (epsilon 3)	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9458051
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519123
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000494	abnormal cecum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12949501
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000643	absent adrenal medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000645	absent adrenergic chromaffin cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0000646	enlarged adrenocortical cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165507
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165507
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165507
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519123
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17504935
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232675
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623560
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001742	absent circulating adrenaline		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357937
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623560
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17683525
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232675
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9604929
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232675
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001753	hypersecretion of corticotropin-releasing hormone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653054
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653054
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623560
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12495930
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12133953
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234455
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002324	abnormal alveolocapillary membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623560
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002768	small adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0003075	abnormal response to CNS ischemic injury		IAGP		N	RGD:5509061	20161103	MGI			PMID:23637179
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0003115	abnormal respiratory system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0003367	increased circulating glucocorticoid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0003711	pathological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0004202	pulmonary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0004733	abnormal thoracic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523311
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519123
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653054
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005129	increased adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471508
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523311
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005345	abnormal circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232675
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0005664	decreased circulating noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357937
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15471946
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0006375	increased circulating angiotensinogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16424199
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523311
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653054
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653054
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653054
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20161103	MGI			PMID:23637179
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519123
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008292	enlarged adrenocortical cell nuclei		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008293	abnormal adrenal gland zona glomerulosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008294	abnormal adrenal gland zona fasciculata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008295	abnormal adrenal gland zona reticularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008302	thin adrenal cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519123
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008504	abnormal adrenal chromaffin cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357937
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008504	abnormal adrenal chromaffin cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20161103	MGI			PMID:23637179
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008704	abnormal interleukin-6 secretion		IAGP		N	RGD:5509061	20161103	MGI			PMID:23637179
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12949501
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12949501
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12949501
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12949501
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357937
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12495930
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523311
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10580006
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0009258	abnormal thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165507
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12949501
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15471946
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653054
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234455
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12949501
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0010119	abnormal bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519123
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0010816	decreased type I pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20220915	MGI			PMID:20519123
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011031	abnormal branching involved in terminal bronchiole morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697839
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357937
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165507
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12495930
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12495930
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14578211
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357937
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232675
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:24082121
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0012441	abnormal monocyte cell number		IAGP		N	RGD:5509061	20161103	MGI			PMID:23637179
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20220915	MGI			PMID:20519123
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0014286	increased adrenal gland zona fasciculata size		IAGP		N	RGD:5509061	20230907	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0014287	decreased adrenal gland zona fasciculata size		IAGP		N	RGD:5509061	20230907	MGI			PMID:19017639
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0030762	decreased adrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:7628695
10691	Nr3c1	nuclear receptor subfamily 3, group C, member 1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:24082121
10693	Gspt1	G1 to S phase transition 1	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
10693	Gspt1	G1 to S phase transition 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20241121	MGI			
10693	Gspt1	G1 to S phase transition 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
10693	Gspt1	G1 to S phase transition 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
10694	Gss	glutathione synthetase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21802407
10697	Gstm1	glutathione S-transferase, mu 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178820
10697	Gstm1	glutathione S-transferase, mu 1	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178820
10697	Gstm1	glutathione S-transferase, mu 1	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178820
10697	Gstm1	glutathione S-transferase, mu 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178820
10697	Gstm1	glutathione S-transferase, mu 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178820
10697	Gstm1	glutathione S-transferase, mu 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:16760226
10697	Gstm1	glutathione S-transferase, mu 1	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178820
10697	Gstm1	glutathione S-transferase, mu 1	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178820
10697	Gstm1	glutathione S-transferase, mu 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:20178820
10700	Gstt1	glutathione S-transferase, theta 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
10700	Gstt1	glutathione S-transferase, theta 1	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20260402	MGI			
10700	Gstt1	glutathione S-transferase, theta 1	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
10700	Gstt1	glutathione S-transferase, theta 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:17827337
10706	Hdc	histidine decarboxylase	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0000336	decreased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11478947
10706	Hdc	histidine decarboxylase	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11478947
10706	Hdc	histidine decarboxylase	gene	MP:0000361	decreased mast cell protease storage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11478947
10706	Hdc	histidine decarboxylase	gene	MP:0000362	decreased mast cell histamine storage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11478947
10706	Hdc	histidine decarboxylase	gene	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24411733
10706	Hdc	histidine decarboxylase	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16310870
10706	Hdc	histidine decarboxylase	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16412995
10706	Hdc	histidine decarboxylase	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16310870
10706	Hdc	histidine decarboxylase	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16310870
10706	Hdc	histidine decarboxylase	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20151210	MGI			PMID:24411733
10706	Hdc	histidine decarboxylase	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16212954
10706	Hdc	histidine decarboxylase	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16310870
10706	Hdc	histidine decarboxylase	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16412995
10706	Hdc	histidine decarboxylase	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:16212954
10706	Hdc	histidine decarboxylase	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16412995
10706	Hdc	histidine decarboxylase	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22993424
10706	Hdc	histidine decarboxylase	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22993424
10706	Hdc	histidine decarboxylase	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24411733
10706	Hdc	histidine decarboxylase	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22993424
10706	Hdc	histidine decarboxylase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16212954
10706	Hdc	histidine decarboxylase	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20151210	MGI			PMID:24411733
10706	Hdc	histidine decarboxylase	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960041
10706	Hdc	histidine decarboxylase	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22993424
10706	Hdc	histidine decarboxylase	gene	MP:0013894	abnormal behavioral response to amphetamine		IAGP		N	RGD:5509061	20151210	MGI			PMID:24411733
10707	Hexa	hexosaminidase A	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
10707	Hexa	hexosaminidase A	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
10707	Hexa	hexosaminidase A	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
10707	Hexa	hexosaminidase A	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
10707	Hexa	hexosaminidase A	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8747922
10707	Hexa	hexosaminidase A	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
10707	Hexa	hexosaminidase A	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14972652
10707	Hexa	hexosaminidase A	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
10707	Hexa	hexosaminidase A	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:14972652
10707	Hexa	hexosaminidase A	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:14972652
10707	Hexa	hexosaminidase A	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14972652
10707	Hexa	hexosaminidase A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9645704
10707	Hexa	hexosaminidase A	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:14972652
10707	Hexa	hexosaminidase A	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
10707	Hexa	hexosaminidase A	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7937929
10707	Hexa	hexosaminidase A	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9645704
10707	Hexa	hexosaminidase A	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14972652
10707	Hexa	hexosaminidase A	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14972652
10707	Hexa	hexosaminidase A	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7937929
10707	Hexa	hexosaminidase A	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8747922
10707	Hexa	hexosaminidase A	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
10707	Hexa	hexosaminidase A	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
10707	Hexa	hexosaminidase A	gene	MP:0003807	camptodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0004676	wide ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:8896570
10707	Hexa	hexosaminidase A	gene	MP:0030262	frontal bossing		IAGP		N	RGD:5509061	20171026	MGI			PMID:8896570
10708	Hgf	hepatocyte growth factor	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854453
10708	Hgf	hepatocyte growth factor	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0000608	dissociated hepatocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854453
10708	Hgf	hepatocyte growth factor	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854453
10708	Hgf	hepatocyte growth factor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15383179
10708	Hgf	hepatocyte growth factor	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854453
10708	Hgf	hepatocyte growth factor	gene	MP:0004300	abnormal organ of Corti supporting cell morphology		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0004364	thin stria vascularis		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0004367	abnormal strial intermediate cell morphology		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0004864	spiral ligament degeneration		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15383179
10708	Hgf	hepatocyte growth factor	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20200813	MGI			PMID:32152201
10708	Hgf	hepatocyte growth factor	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854453
10708	Hgf	hepatocyte growth factor	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10708	Hgf	hepatocyte growth factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10708	Hgf	hepatocyte growth factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854453
10708	Hgf	hepatocyte growth factor	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:7854452
10710	Hk1	hexokinase 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0002814	hyperchromasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11783948
10710	Hk1	hexokinase 1	gene	MP:0014990	enhanced erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:11783948
10711	Hmgb1	high mobility group box 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391216
10711	Hmgb1	high mobility group box 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391216
10711	Hmgb1	high mobility group box 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391216
10711	Hmgb1	high mobility group box 1	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391216
10711	Hmgb1	high mobility group box 1	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391216
10711	Hmgb1	high mobility group box 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0002715	decreased glycogen catabolism rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391216
10711	Hmgb1	high mobility group box 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649368
10711	Hmgb1	high mobility group box 1	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20160204	MGI			PMID:24361123
10711	Hmgb1	high mobility group box 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391216
10711	Hmgb1	high mobility group box 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391216
10711	Hmgb1	high mobility group box 1	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24361123
10711	Hmgb1	high mobility group box 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24361123
10711	Hmgb1	high mobility group box 1	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0008684	increased interleukin-18 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0008806	increased circulating amylase level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24361123
10711	Hmgb1	high mobility group box 1	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0009148	pancreas necrosis		IAGP		N	RGD:5509061	20160204	MGI			PMID:24361123
10711	Hmgb1	high mobility group box 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20260402	MGI			
10711	Hmgb1	high mobility group box 1	gene	MP:0011080	increased macrophage apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10391216
10711	Hmgb1	high mobility group box 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302768
10711	Hmgb1	high mobility group box 1	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24361123
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0003457	abnormal circulating ketone body level		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20200528	MGI			PMID:31910233
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0013483	abnormal jejunum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0013485	increased Paneth cell number		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0013798	abnormal jejunal goblet cell morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0014508	decreased intestinal crypt stem cell number		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0014509	abnormal intestinal crypt stem cell physiology		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20220901	MGI			PMID:35421611
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0031319	impaired intestine regeneration		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10713	Hmgcs2	3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2	gene	MP:0031320	enhanced intestine regeneration		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20151203	MGI			PMID:25750434
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534534
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20151203	MGI			PMID:25750434
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20151203	MGI			PMID:25750434
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14534534
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20151203	MGI			PMID:25750434
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20190502	MGI			
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20151203	MGI			PMID:25750434
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:25750434
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:25750434
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20151203	MGI			PMID:25750434
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20151203	MGI			PMID:25750434
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
10714	Hmmr	hyaluronan mediated motility receptor (RHAMM)	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:25750434
10717	Hmox1	heme oxygenase 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20201022	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273999
10717	Hmox1	heme oxygenase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210610	MGI			PMID:31571584
10717	Hmox1	heme oxygenase 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20210610	MGI			PMID:31571584
10717	Hmox1	heme oxygenase 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230601	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385506
10717	Hmox1	heme oxygenase 1	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706490
10717	Hmox1	heme oxygenase 1	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273999
10717	Hmox1	heme oxygenase 1	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273999
10717	Hmox1	heme oxygenase 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20210610	MGI			PMID:31571584
10717	Hmox1	heme oxygenase 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0003326	liver failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706490
10717	Hmox1	heme oxygenase 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10807584
10717	Hmox1	heme oxygenase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20220519	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24630724
10717	Hmox1	heme oxygenase 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20210610	MGI			PMID:31571584
10717	Hmox1	heme oxygenase 1	gene	MP:0003913	increased heart right ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10807584
10717	Hmox1	heme oxygenase 1	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10807584
10717	Hmox1	heme oxygenase 1	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20210826	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706490
10717	Hmox1	heme oxygenase 1	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10807584
10717	Hmox1	heme oxygenase 1	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385506
10717	Hmox1	heme oxygenase 1	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273999
10717	Hmox1	heme oxygenase 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0010750	increased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706490
10717	Hmox1	heme oxygenase 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207174
10717	Hmox1	heme oxygenase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273999
10717	Hmox1	heme oxygenase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210610	MGI			PMID:31571584
10717	Hmox1	heme oxygenase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0011352	proximal convoluted tubule brush border loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10807584
10717	Hmox1	heme oxygenase 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:10807584
10717	Hmox1	heme oxygenase 1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20201022	MGI			
10717	Hmox1	heme oxygenase 1	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0011854	cerebral edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706490
10717	Hmox1	heme oxygenase 1	gene	MP:0011890	increased circulating ferritin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380735
10717	Hmox1	heme oxygenase 1	gene	MP:0020953	decreased susceptibility to Paramyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:19398754
10717	Hmox1	heme oxygenase 1	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:24995976
10717	Hmox1	heme oxygenase 1	gene	MP:0031510	increased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:11385506
10718	Foxa1	forkhead box A1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18381283
10718	Foxa1	forkhead box A1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10049364
10718	Foxa1	forkhead box A1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:20501593
10718	Foxa1	forkhead box A1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10718	Foxa1	forkhead box A1	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10049364
10718	Foxa1	forkhead box A1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10049364
10718	Foxa1	forkhead box A1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10049364
10718	Foxa1	forkhead box A1	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10718	Foxa1	forkhead box A1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12395314
10718	Foxa1	forkhead box A1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10049364
10718	Foxa1	forkhead box A1	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265403
10718	Foxa1	forkhead box A1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10718	Foxa1	forkhead box A1	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10718	Foxa1	forkhead box A1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265403
10718	Foxa1	forkhead box A1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265403
10718	Foxa1	forkhead box A1	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0005492	exocrine pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10718	Foxa1	forkhead box A1	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10718	Foxa1	forkhead box A1	gene	MP:0009169	pancreatic islet hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10718	Foxa1	forkhead box A1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10049364
10718	Foxa1	forkhead box A1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468578
10718	Foxa1	forkhead box A1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10718	Foxa1	forkhead box A1	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:20501593
10718	Foxa1	forkhead box A1	gene	MP:0014161	increased circulating cortisol level		IAGP		N	RGD:5509061	20160414	MGI			PMID:10468578
10719	Foxa2	forkhead box A2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680365
10719	Foxa2	forkhead box A2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757645
10719	Foxa2	forkhead box A2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
10719	Foxa2	forkhead box A2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846474
10719	Foxa2	forkhead box A2	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680365
10719	Foxa2	forkhead box A2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15616563
10719	Foxa2	forkhead box A2	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15616563
10719	Foxa2	forkhead box A2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10719	Foxa2	forkhead box A2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9825865
10719	Foxa2	forkhead box A2	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
10719	Foxa2	forkhead box A2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
10719	Foxa2	forkhead box A2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
10719	Foxa2	forkhead box A2	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10719	Foxa2	forkhead box A2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15616563
10719	Foxa2	forkhead box A2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866673
10719	Foxa2	forkhead box A2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304540
10719	Foxa2	forkhead box A2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18161057
10719	Foxa2	forkhead box A2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359409
10719	Foxa2	forkhead box A2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23712942
10719	Foxa2	forkhead box A2	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11291865
10719	Foxa2	forkhead box A2	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0002234	abnormal pharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0002281	abnormal respiratory mucosa goblet cell morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:30923168
10719	Foxa2	forkhead box A2	gene	MP:0002314	abnormal respiratory mechanics		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757645
10719	Foxa2	forkhead box A2	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20200402	MGI			PMID:30923168
10719	Foxa2	forkhead box A2	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680365
10719	Foxa2	forkhead box A2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
10719	Foxa2	forkhead box A2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265403
10719	Foxa2	forkhead box A2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10719	Foxa2	forkhead box A2	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0003653	decreased skin turgor		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680365
10719	Foxa2	forkhead box A2	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
10719	Foxa2	forkhead box A2	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10719	Foxa2	forkhead box A2	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22529374
10719	Foxa2	forkhead box A2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18161057
10719	Foxa2	forkhead box A2	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
10719	Foxa2	forkhead box A2	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
10719	Foxa2	forkhead box A2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265403
10719	Foxa2	forkhead box A2	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265403
10719	Foxa2	forkhead box A2	gene	MP:0004554	small pharynx		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0004781	abnormal surfactant composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0004831	long incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200402	MGI			PMID:30923168
10719	Foxa2	forkhead box A2	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11291865
10719	Foxa2	forkhead box A2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15616563
10719	Foxa2	forkhead box A2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757645
10719	Foxa2	forkhead box A2	gene	MP:0005440	increased glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0005492	exocrine pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10719	Foxa2	forkhead box A2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757645
10719	Foxa2	forkhead box A2	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0006344	small second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20161027	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0009021	absent estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
10719	Foxa2	forkhead box A2	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10719	Foxa2	forkhead box A2	gene	MP:0009163	absent pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:22529374
10719	Foxa2	forkhead box A2	gene	MP:0009169	pancreatic islet hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10719	Foxa2	forkhead box A2	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22529374
10719	Foxa2	forkhead box A2	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680365
10719	Foxa2	forkhead box A2	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680365
10719	Foxa2	forkhead box A2	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846474
10719	Foxa2	forkhead box A2	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:11291865
10719	Foxa2	forkhead box A2	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15616563
10719	Foxa2	forkhead box A2	gene	MP:0009667	abnormal embryo invasion		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
10719	Foxa2	forkhead box A2	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
10719	Foxa2	forkhead box A2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0010355	abnormal first pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
10719	Foxa2	forkhead box A2	gene	MP:0010549	absent dorsal mesocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0010814	absent alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0010817	absent type I pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0010856	dilated respiratory conducting tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757645
10719	Foxa2	forkhead box A2	gene	MP:0010861	increased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757645
10719	Foxa2	forkhead box A2	gene	MP:0010896	decreased lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757645
10719	Foxa2	forkhead box A2	gene	MP:0010935	increased airway resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757645
10719	Foxa2	forkhead box A2	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0011018	pulmonary hyaline membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445544
10719	Foxa2	forkhead box A2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680365
10719	Foxa2	forkhead box A2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19141476
10719	Foxa2	forkhead box A2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757645
10719	Foxa2	forkhead box A2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18161057
10719	Foxa2	forkhead box A2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846474
10719	Foxa2	forkhead box A2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956259
10719	Foxa2	forkhead box A2	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18161057
10719	Foxa2	forkhead box A2	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069909
10719	Foxa2	forkhead box A2	gene	MP:0012263	decreased hindbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0012271	abnormal chordamesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8069910
10719	Foxa2	forkhead box A2	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11291865
10719	Foxa2	forkhead box A2	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
10719	Foxa2	forkhead box A2	gene	MP:0013400	abnormal endometrial gland development		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
10719	Foxa2	forkhead box A2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:9825865
10719	Foxa2	forkhead box A2	gene	MP:0014473	increased pulmonary alveolus wall thickness		IAGP		N	RGD:5509061	20240704	MGI			PMID:15452354
10719	Foxa2	forkhead box A2	gene	MP:0031434	increased miscarriage rate		IAGP		N	RGD:5509061	20220915	MGI			PMID:8069910
10720	Foxa3	forkhead box A3	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20181220	MGI			PMID:17488644
10720	Foxa3	forkhead box A3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20181220	MGI			PMID:17488644
10720	Foxa3	forkhead box A3	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20181220	MGI			PMID:17488644
10720	Foxa3	forkhead box A3	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9632808
10720	Foxa3	forkhead box A3	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:17488644
10720	Foxa3	forkhead box A3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:17488644
10720	Foxa3	forkhead box A3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0008390	abnormal primordial germ cell proliferation		IAGP		N	RGD:5509061	20181220	MGI			PMID:17488644
10720	Foxa3	forkhead box A3	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:17488644
10720	Foxa3	forkhead box A3	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20181220	MGI			PMID:11546810
10720	Foxa3	forkhead box A3	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20181220	MGI			PMID:17488644
10720	Foxa3	forkhead box A3	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0020103	decreased hepatic glucose production		IAGP		N	RGD:5509061	20181220	MGI			PMID:11546810
10720	Foxa3	forkhead box A3	gene	MP:0020325	abnormal beige fat cell morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10720	Foxa3	forkhead box A3	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20181220	MGI			PMID:25225406
10721	Onecut1	one cut domain, family member 1	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934848
10721	Onecut1	one cut domain, family member 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400205
10721	Onecut1	one cut domain, family member 1	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934848
10721	Onecut1	one cut domain, family member 1	gene	MP:0003250	absent gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934848
10721	Onecut1	one cut domain, family member 1	gene	MP:0003266	biliary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103213
10721	Onecut1	one cut domain, family member 1	gene	MP:0003334	pancreas fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:23926259
10721	Onecut1	one cut domain, family member 1	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781686
10721	Onecut1	one cut domain, family member 1	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400205
10721	Onecut1	one cut domain, family member 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0005083	abnormal biliary tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934848
10721	Onecut1	one cut domain, family member 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:23926259
10721	Onecut1	one cut domain, family member 1	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:23926259
10721	Onecut1	one cut domain, family member 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:23926259
10721	Onecut1	one cut domain, family member 1	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:23926259
10721	Onecut1	one cut domain, family member 1	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781686
10721	Onecut1	one cut domain, family member 1	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400205
10721	Onecut1	one cut domain, family member 1	gene	MP:0009143	abnormal pancreatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0009145	abnormal pancreatic acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0009149	decreased pancreatic acinar cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0009164	exocrine pancreas atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0009173	absent pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0009174	absent pancreatic beta cells		IAGP		N	RGD:5509061	20150305	MGI			PMID:17400205
10721	Onecut1	one cut domain, family member 1	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0009178	absent pancreatic alpha cells		IAGP		N	RGD:5509061	20150305	MGI			PMID:17400205
10721	Onecut1	one cut domain, family member 1	gene	MP:0009181	decreased pancreatic delta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10825208
10721	Onecut1	one cut domain, family member 1	gene	MP:0011932	abnormal endocrine pancreas development		IAGP		N	RGD:5509061	20150305	MGI			PMID:17400205
10721	Onecut1	one cut domain, family member 1	gene	MP:0011934	abnormal branching involved in pancreas development		IAGP		N	RGD:5509061	20160324	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200123	MGI			PMID:23926259
10721	Onecut1	one cut domain, family member 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200123	MGI			PMID:23926259
10721	Onecut1	one cut domain, family member 1	gene	MP:0012242	abnormal hepatoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103213
10721	Onecut1	one cut domain, family member 1	gene	MP:0012246	abnormal hepatic cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103213
10721	Onecut1	one cut domain, family member 1	gene	MP:0013221	pancreatic acinar-to-ductal metaplasia		IAGP		N	RGD:5509061	20160324	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0014092	abnormal pancreatic primary cilium morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0014094	decreased pancreatic primary cilium number		IAGP		N	RGD:5509061	20190718	MGI			PMID:19766716
10721	Onecut1	one cut domain, family member 1	gene	MP:0014108	calcified pancreas		IAGP		N	RGD:5509061	20160324	MGI			PMID:19766716
10724	Hoxc	homeobox C cluster	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0004614	caudal vertebral transformation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10724	Hoxc	homeobox C cluster	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20111116	MGI			PMID:10753520
10728	Hp	haptoglobin	gene	MP:0000332	hemoglobinemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731043
10728	Hp	haptoglobin	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393471
10728	Hp	haptoglobin	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393471
10728	Hp	haptoglobin	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731043
10728	Hp	haptoglobin	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793279
10728	Hp	haptoglobin	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731043
10728	Hp	haptoglobin	gene	MP:0003193	decreased cholesterol efflux		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082477
10728	Hp	haptoglobin	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176700
10728	Hp	haptoglobin	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176700
10728	Hp	haptoglobin	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176700
10728	Hp	haptoglobin	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068284
10728	Hp	haptoglobin	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393471
10728	Hp	haptoglobin	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176700
10728	Hp	haptoglobin	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393471
10728	Hp	haptoglobin	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393471
10728	Hp	haptoglobin	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731043
10728	Hp	haptoglobin	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393471
10728	Hp	haptoglobin	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865977
10728	Hp	haptoglobin	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793279
10728	Hp	haptoglobin	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068284
10728	Hp	haptoglobin	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731043
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12427827
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238881
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059342
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002649	abnormal enamel rod pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0003108	short zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0003769	abnormal lip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10871846
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0010234	abnormal vibrissa follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20160811	MGI			PMID:26359368
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059342
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059342
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0011471	decreased urine creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:20179099
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030034	depressed nasal bridge		IAGP		N	RGD:5509061	20170914	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030036	short nasal bridge		IAGP		N	RGD:5509061	20170914	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030062	choanal stenosis		IAGP		N	RGD:5509061	20170921	MGI			PMID:18483625
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030199	deviated nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030219	jaw cyst		IAGP		N	RGD:5509061	20171019	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20171221	MGI			PMID:19416908
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20171221	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030471	abnormal ameloblast differentiation		IAGP		N	RGD:5509061	20180118	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030521	abnormal cervical loop morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030522	abnormal stellate reticulum morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0030523	abnormal stratum intermedium morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:24057668
10730	Hras	Hras proto-oncogene, GTPase	gene	MP:0031232	increased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:18483625
10731	Hrh1	histamine receptor H1	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
10731	Hrh1	histamine receptor H1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:8917588
10731	Hrh1	histamine receptor H1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20150129	MGI			PMID:12142541
10731	Hrh1	histamine receptor H1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989982
10731	Hrh1	histamine receptor H1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680192
10731	Hrh1	histamine receptor H1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
10731	Hrh1	histamine receptor H1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20150129	MGI			PMID:12142541
10731	Hrh1	histamine receptor H1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680192
10731	Hrh1	histamine receptor H1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680192
10731	Hrh1	histamine receptor H1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8917588
10731	Hrh1	histamine receptor H1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8917588
10731	Hrh1	histamine receptor H1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989982
10731	Hrh1	histamine receptor H1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20150129	MGI			PMID:12142541
10731	Hrh1	histamine receptor H1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989982
10731	Hrh1	histamine receptor H1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989982
10731	Hrh1	histamine receptor H1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989982
10731	Hrh1	histamine receptor H1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680192
10731	Hrh1	histamine receptor H1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989982
10731	Hrh1	histamine receptor H1	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680192
10731	Hrh1	histamine receptor H1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989982
10731	Hrh1	histamine receptor H1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989982
10731	Hrh1	histamine receptor H1	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680192
10731	Hrh1	histamine receptor H1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20150129	MGI			PMID:12142541
10731	Hrh1	histamine receptor H1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0011943	abnormal circadian feeding behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331534
10731	Hrh1	histamine receptor H1	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20171012	MGI			PMID:8917588
10731	Hrh1	histamine receptor H1	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:15331534
10732	Hrh2	histamine receptor H2	gene	MP:0000505	decreased digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862789
10732	Hrh2	histamine receptor H2	gene	MP:0000505	decreased digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0003892	abnormal gastric gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0004138	abnormal mucous neck cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862789
10732	Hrh2	histamine receptor H2	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0004731	increased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862789
10732	Hrh2	histamine receptor H2	gene	MP:0004731	increased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0005211	increased stomach mucosa thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862789
10732	Hrh2	histamine receptor H2	gene	MP:0008004	abnormal stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862789
10732	Hrh2	histamine receptor H2	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862789
10732	Hrh2	histamine receptor H2	gene	MP:0010799	stomach mucosa hyperplasia		IAGP		N	RGD:5509061	20150312	MGI			PMID:12729842
10732	Hrh2	histamine receptor H2	gene	MP:0013569	gastric gland hyperplasia		IAGP		N	RGD:5509061	20150312	MGI			PMID:12729842
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047607
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11546766
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047607
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:22555437
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405715
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274359
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12439781
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22555437
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274359
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383297
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11546766
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047607
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22555437
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23832962
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20151224	MGI			PMID:24667799
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0002078	abnormal glucose homeostasis		IEA		N	RGD:5509061	20111116	MGI			
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11546766
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12439781
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11546766
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11546766
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22555437
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22555437
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383297
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383297
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11165006
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405715
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20151224	MGI			PMID:24667799
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383297
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11546766
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274359
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22555437
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11546766
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047607
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383297
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:24169553
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405715
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779947
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047607
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23832962
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0008243	abnormal macrophage derived foam cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383297
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383297
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383297
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0009428	decreased tibialis anterior weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23832962
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20150611	MGI			PMID:9405715
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106871
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0010814	absent alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:12439781
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0010889	small alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:12439781
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12439781
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20151224	MGI			PMID:24667799
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12439781
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0011702	abnormal fibroblast proliferation		IAGP		N	RGD:5509061	20151224	MGI			PMID:24667799
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20151224	MGI			PMID:24667799
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:24169553
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0012172	abnormal amniotic fluid composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:12439781
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22555437
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0014970	decreased muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22555437
10734	Hsd11b1	hydroxysteroid 11-beta dehydrogenase 1	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20151224	MGI			PMID:24667799
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16896181
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23741059
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23741059
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250605	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0005628	decreased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0009051	dilated distal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0011471	decreased urine creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10074485
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:23741059
10735	Hsd11b2	hydroxysteroid 11-beta dehydrogenase 2	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:23741059
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0001516	abnormal motor coordination/balance		IEA		N	RGD:5509061	20190502	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20170105	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0002679	abnormal corpus luteum morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20170105	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20210520	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0004855	increased ovary weight		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0004903	abnormal uterus weight		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0005133	increased luteinizing hormone level		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20170105	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0011384	abnormal progesterone level		IAGP		N	RGD:5509061	20160602	MGI			PMID:26018678
10736	Hsd17b1	hydroxysteroid (17-beta) dehydrogenase 1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20170105	MGI			
10740	Hspa2	heat shock protein family A (Hsp70) member 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622925
10740	Hspa2	heat shock protein family A (Hsp70) member 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622925
10740	Hspa2	heat shock protein family A (Hsp70) member 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622925
10740	Hspa2	heat shock protein family A (Hsp70) member 2	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622925
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847323
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158912
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158912
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158912
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847323
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847323
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158912
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033462
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033462
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847323
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847323
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0010909	pulmonary alveolar hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464327
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22821687
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847323
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158912
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847323
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
10742	Hspa5	heat shock protein family A (Hsp70) member 5	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:22821687
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751426
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152131
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724773
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9826725
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844013
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121072
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997373
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11080193
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9826725
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844013
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507009
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844013
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121072
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751426
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121072
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0005322	abnormal serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11080193
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0005322	abnormal serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483665
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0006276	abnormal autonomic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0009436	fragmentation of sleep/wake states		IAGP		N	RGD:5509061	20220922	MGI			PMID:23997373
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0012287	increased frequency of paradoxical sleep		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997373
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0012291	increased slow-wave sleep duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997373
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0012575	increased noradrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:11080193
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0014638	increased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:23997373
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:20152131
10745	Htr1a	5-hydroxytryptamine (serotonin) receptor 1A	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:9724773
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11790410
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164514
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11790410
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:8091214
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996411
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12798274
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164514
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12742250
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220519	MGI			
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12798274
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0003958	heart valve hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19041748
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19041748
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:11790410
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:19041748
10746	Htr1b	5-hydroxytryptamine (serotonin) receptor 1B	gene	MP:0030438	increased osteoblast proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:19041748
10747	Htr1d	5-hydroxytryptamine (serotonin) receptor 1D	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
10747	Htr1d	5-hydroxytryptamine (serotonin) receptor 1D	gene	MP:0005379	endocrine/exocrine gland phenotype		IAGP		N	RGD:5509061	20200402	MGI			PMID:31806625
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0000421	mottled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844009
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844009
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844009
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20260129	MGI			PMID:38941473
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001492	abnormal pilomotor reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20160317	MGI			PMID:25257581
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20160317	MGI			PMID:25257581
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20160317	MGI			PMID:25257581
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005535	abnormal body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0008431	abnormal short-term spatial reference memory		IAGP		N	RGD:5509061	20260129	MGI			PMID:38941473
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771748
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20260129	MGI			PMID:38941473
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038216
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700379
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0011612	increased circulating ghrelin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:24177424
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:20394819
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:19036977
10748	Htr2c	5-hydroxytryptamine (serotonin) receptor 2C	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:19036977
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0001761	abnormal urination pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0003043	hypoalgesia		IEA		N	RGD:5509061	20220519	MGI			
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0003280	urinary incontinence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0003608	prostate gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0005302	neurogenic bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:11826129
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0009552	urinary bladder obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0010386	abnormal urinary bladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0011403	pyelonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0011774	abnormal urinary bladder detrusor smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0011777	abnormal male prostatic urethra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0011784	abnormal urinary bladder neck morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0011799	increased urinary bladder weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0011801	urethra obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10749	Htr3a	5-hydroxytryptamine (serotonin) receptor 3A	gene	MP:0011802	seminal vesiculitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201326
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724239
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724239
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724239
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724239
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724239
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724239
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20180531	MGI			PMID:17913892
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20111116	MGI			
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20180531	MGI			PMID:17913892
10750	Htr4	5 hydroxytryptamine (serotonin) receptor 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724239
10751	Htr5a	5-hydroxytryptamine (serotonin) receptor 5A	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10197537
10751	Htr5a	5-hydroxytryptamine (serotonin) receptor 5A	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
10751	Htr5a	5-hydroxytryptamine (serotonin) receptor 5A	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20141003	MGI			PMID:10197537
10754	Iapp	islet amyloid polypeptide	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970190
10754	Iapp	islet amyloid polypeptide	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970190
10754	Iapp	islet amyloid polypeptide	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970190
10754	Iapp	islet amyloid polypeptide	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970190
10754	Iapp	islet amyloid polypeptide	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9753619
10754	Iapp	islet amyloid polypeptide	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9753619
10754	Iapp	islet amyloid polypeptide	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970190
10754	Iapp	islet amyloid polypeptide	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970190
10754	Iapp	islet amyloid polypeptide	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970190
10754	Iapp	islet amyloid polypeptide	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9753619
10754	Iapp	islet amyloid polypeptide	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970190
10754	Iapp	islet amyloid polypeptide	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:14970190
10755	Ibsp	integrin binding sialoprotein	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20180201	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20160804	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20160804	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20160804	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20160804	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20160804	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20160804	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20160804	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0010929	increased osteoid thickness		IAGP		N	RGD:5509061	20160804	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0011165	abnormal tooth root development		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20220915	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20160804	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:18458111
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030131	abnormal periodontium morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030351	wide coronal suture		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030357	wide lambdoid suture		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030393	delayed fontanelle closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030452	abnormal cementum mineralization		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030466	alveolar process atrophy		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030466	alveolar process atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030494	abnormal molar root morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030516	abnormal junctional epithelium morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030524	abnormal tooth root resorption		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030524	abnormal tooth root resorption		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20180125	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20180201	MGI			PMID:25963390
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030545	abnormal acellular cementum morphology		IAGP		N	RGD:5509061	20180208	MGI			PMID:23183644
10755	Ibsp	integrin binding sialoprotein	gene	MP:0030545	abnormal acellular cementum morphology		IAGP		N	RGD:5509061	20180208	MGI			PMID:25963390
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634125
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8551244
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634125
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7535798
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7911822
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8104338
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636189
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636189
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636189
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766082
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10670575
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8104338
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17595378
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17595378
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17595378
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7911822
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15229332
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17595378
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17595378
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934241
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17291995
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7535798
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16731772
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003434	decreased susceptibility to induced choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766082
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003627	abnormal leukocyte tethering or rolling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634125
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003627	abnormal leukocyte tethering or rolling		IAGP		N	RGD:5509061	20141003	MGI			PMID:8551244
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003627	abnormal leukocyte tethering or rolling		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636189
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634125
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16412045
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17595378
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20160128	MGI			PMID:26034041
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17291995
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120869
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636189
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7911822
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636189
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005580	periinsulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120869
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17291995
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17595378
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7911822
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8104338
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17291995
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16731772
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847222
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7911822
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7911822
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7911822
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8104338
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636189
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12769195
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0011825	decreased cell chemotaxis		IAGP		N	RGD:5509061	20160128	MGI			PMID:26034041
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0012194	decreased keratinocyte migration		IAGP		N	RGD:5509061	20141204	MGI			PMID:17595378
10756	Icam1	intercellular adhesion molecule 1	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:8551244
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:25730874
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20150528	MGI			PMID:25730874
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150528	MGI			PMID:25730874
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0002414	abnormal myeloblast morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:25730874
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:25730874
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763442
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150528	MGI			PMID:25730874
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150528	MGI			PMID:25730874
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10758	Idh1	isocitrate dehydrogenase 1 (NADP+), soluble	gene	MP:0012514	pectus excavatum		IAGP		N	RGD:5509061	20150528	MGI			PMID:25730874
10759	Idh3g	isocitrate dehydrogenase 3 (NAD+), gamma	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
10765	Igf1	insulin-like growth factor 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10765	Igf1	insulin-like growth factor 1	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10765	Igf1	insulin-like growth factor 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10765	Igf1	insulin-like growth factor 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10765	Igf1	insulin-like growth factor 1	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235108
10765	Igf1	insulin-like growth factor 1	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15597051
10765	Igf1	insulin-like growth factor 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15597051
10765	Igf1	insulin-like growth factor 1	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20382057
10765	Igf1	insulin-like growth factor 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0001238	thin epidermis stratum spinosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10765	Igf1	insulin-like growth factor 1	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235108
10765	Igf1	insulin-like growth factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14741342
10765	Igf1	insulin-like growth factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033454
10765	Igf1	insulin-like growth factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8958230
10765	Igf1	insulin-like growth factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10765	Igf1	insulin-like growth factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10765	Igf1	insulin-like growth factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033454
10765	Igf1	insulin-like growth factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10765	Igf1	insulin-like growth factor 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033454
10765	Igf1	insulin-like growth factor 1	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20382057
10765	Igf1	insulin-like growth factor 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10765	Igf1	insulin-like growth factor 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048072
10765	Igf1	insulin-like growth factor 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8276243
10765	Igf1	insulin-like growth factor 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731712
10765	Igf1	insulin-like growth factor 1	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8276243
10765	Igf1	insulin-like growth factor 1	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8276243
10765	Igf1	insulin-like growth factor 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8276243
10765	Igf1	insulin-like growth factor 1	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235108
10765	Igf1	insulin-like growth factor 1	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8276243
10765	Igf1	insulin-like growth factor 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8276243
10765	Igf1	insulin-like growth factor 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7718235
10765	Igf1	insulin-like growth factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377413
10765	Igf1	insulin-like growth factor 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0002679	abnormal corpus luteum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8958230
10765	Igf1	insulin-like growth factor 1	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235108
10765	Igf1	insulin-like growth factor 1	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10765	Igf1	insulin-like growth factor 1	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10765	Igf1	insulin-like growth factor 1	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235108
10765	Igf1	insulin-like growth factor 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10765	Igf1	insulin-like growth factor 1	gene	MP:0003429	insensitivity to growth hormone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048072
10765	Igf1	insulin-like growth factor 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7718235
10765	Igf1	insulin-like growth factor 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10765	Igf1	insulin-like growth factor 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235108
10765	Igf1	insulin-like growth factor 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033454
10765	Igf1	insulin-like growth factor 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535874
10765	Igf1	insulin-like growth factor 1	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0003986	small cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731712
10765	Igf1	insulin-like growth factor 1	gene	MP:0004664	delayed inner ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359843
10765	Igf1	insulin-like growth factor 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535874
10765	Igf1	insulin-like growth factor 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033454
10765	Igf1	insulin-like growth factor 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048072
10765	Igf1	insulin-like growth factor 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20382057
10765	Igf1	insulin-like growth factor 1	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14741342
10765	Igf1	insulin-like growth factor 1	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0004716	abnormal cochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567053
10765	Igf1	insulin-like growth factor 1	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16420467
10765	Igf1	insulin-like growth factor 1	gene	MP:0004750	syndromic hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16420467
10765	Igf1	insulin-like growth factor 1	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8958230
10765	Igf1	insulin-like growth factor 1	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10765	Igf1	insulin-like growth factor 1	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535874
10765	Igf1	insulin-like growth factor 1	gene	MP:0005137	increased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14741342
10765	Igf1	insulin-like growth factor 1	gene	MP:0005158	ovary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8958230
10765	Igf1	insulin-like growth factor 1	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535874
10765	Igf1	insulin-like growth factor 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14741342
10765	Igf1	insulin-like growth factor 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048072
10765	Igf1	insulin-like growth factor 1	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:14741342
10765	Igf1	insulin-like growth factor 1	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8958230
10765	Igf1	insulin-like growth factor 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535874
10765	Igf1	insulin-like growth factor 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8958230
10765	Igf1	insulin-like growth factor 1	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535874
10765	Igf1	insulin-like growth factor 1	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235108
10765	Igf1	insulin-like growth factor 1	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033454
10765	Igf1	insulin-like growth factor 1	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235108
10765	Igf1	insulin-like growth factor 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:14741342
10765	Igf1	insulin-like growth factor 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731712
10765	Igf1	insulin-like growth factor 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033454
10765	Igf1	insulin-like growth factor 1	gene	MP:0008831	abnormal insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133160
10765	Igf1	insulin-like growth factor 1	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0009014	prolonged proestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0009018	short estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0009090	myometrium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0009091	endometrium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14741342
10765	Igf1	insulin-like growth factor 1	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14741342
10765	Igf1	insulin-like growth factor 1	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0009364	abnormal mature ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20382057
10765	Igf1	insulin-like growth factor 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10765	Igf1	insulin-like growth factor 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0009947	abnormal olfactory bulb external plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0009954	abnormal mitral cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0010817	absent type I pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20382057
10765	Igf1	insulin-like growth factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10765	Igf1	insulin-like growth factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16420467
10765	Igf1	insulin-like growth factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591604
10765	Igf1	insulin-like growth factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20382057
10765	Igf1	insulin-like growth factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10765	Igf1	insulin-like growth factor 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033454
10765	Igf1	insulin-like growth factor 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10765	Igf1	insulin-like growth factor 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731712
10765	Igf1	insulin-like growth factor 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537147
10765	Igf1	insulin-like growth factor 1	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:16420467
10765	Igf1	insulin-like growth factor 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16420467
10765	Igf1	insulin-like growth factor 1	gene	MP:0013400	abnormal endometrial gland development		IAGP		N	RGD:5509061	20141218	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0014740	increased auditory brainstem response wave peak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:16420467
10765	Igf1	insulin-like growth factor 1	gene	MP:0014742	increased auditory brainstem response wave interpeak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:16420467
10765	Igf1	insulin-like growth factor 1	gene	MP:0031421	increased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:19497975
10765	Igf1	insulin-like growth factor 1	gene	MP:0031635	increased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:8958230
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12930811
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12930811
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12930811
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12930811
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001238	thin epidermis stratum spinosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20170720	MGI			PMID:27861515
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875258
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875258
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875258
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875258
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628051
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20170803	MGI			PMID:28207927
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628051
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0002996	ovotestis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628051
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733797
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004289	abnormal bony labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004396	decreased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004408	decreased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004589	abnormal cochlear hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733797
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20170720	MGI			PMID:27861515
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20170720	MGI			PMID:28655914
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20170803	MGI			PMID:28207927
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0009673	increased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0009728	abnormal calcaneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18443199
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19174523
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010862	decreased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20170803	MGI			PMID:28207927
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010897	abnormal bronchiole epithelium morphology		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010897	abnormal bronchiole epithelium morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:27861515
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20160714	MGI			PMID:25238791
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0011061	abnormal inner hair cell kinocilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806824
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10875258
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159122
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:19174523
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:17189427
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20170803	MGI			PMID:28207927
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20170720	MGI			PMID:28655914
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0030279	thin neurocranium		IAGP		N	RGD:5509061	20171102	MGI			PMID:12215457
10766	Igf1r	insulin-like growth factor I receptor	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:17189427
10766453	Char11_m	P. chabaudi malaria resistance QTL 11 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20160211	MGI			PMID:9398835
10766453	Char11_m	P. chabaudi malaria resistance QTL 11 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:9398835
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20160211	MGI			PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:16943797
10766456	Sle21_m	systematic lupus erythematosus susceptibility 21 (mouse)	qtl	MP:0011508	abnormal glomerular capillary thrombosis		IAGP		N	RGD:5509061	20160211	MGI			PMID:21724994
10766458	Nba12_m	New Zealand Black autoimmunity 12 (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20160211	MGI			PMID:12215897
10766458	Nba12_m	New Zealand Black autoimmunity 12 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:12215897
10770	Igf2	insulin-like growth factor 2	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10770	Igf2	insulin-like growth factor 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10770	Igf2	insulin-like growth factor 2	gene	MP:0001238	thin epidermis stratum spinosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10770	Igf2	insulin-like growth factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10770	Igf2	insulin-like growth factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1997210
10770	Igf2	insulin-like growth factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:2330056
10770	Igf2	insulin-like growth factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7536897
10770	Igf2	insulin-like growth factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10770	Igf2	insulin-like growth factor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11743023
10770	Igf2	insulin-like growth factor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10770	Igf2	insulin-like growth factor 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10770	Igf2	insulin-like growth factor 2	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017078
10770	Igf2	insulin-like growth factor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10770	Igf2	insulin-like growth factor 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017078
10770	Igf2	insulin-like growth factor 2	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11743023
10770	Igf2	insulin-like growth factor 2	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10770	Igf2	insulin-like growth factor 2	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150410
10770	Igf2	insulin-like growth factor 2	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:1997210
10770	Igf2	insulin-like growth factor 2	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10770	Igf2	insulin-like growth factor 2	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10770	Igf2	insulin-like growth factor 2	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11432838
10770	Igf2	insulin-like growth factor 2	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11846487
10770	Igf2	insulin-like growth factor 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12087403
10770	Igf2	insulin-like growth factor 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0004196	abnormal prenatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12087403
10770	Igf2	insulin-like growth factor 2	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:12087403
10770	Igf2	insulin-like growth factor 2	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150410
10770	Igf2	insulin-like growth factor 2	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10770	Igf2	insulin-like growth factor 2	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:12087403
10770	Igf2	insulin-like growth factor 2	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150410
10770	Igf2	insulin-like growth factor 2	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
10770	Igf2	insulin-like growth factor 2	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150410
10770	Igf2	insulin-like growth factor 2	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0009265	delayed eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
10770	Igf2	insulin-like growth factor 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150410
10770	Igf2	insulin-like growth factor 2	gene	MP:0009432	increased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0009673	increased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10770	Igf2	insulin-like growth factor 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10770	Igf2	insulin-like growth factor 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10770	Igf2	insulin-like growth factor 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017078
10770	Igf2	insulin-like growth factor 2	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0010600	enlarged pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0010865	prenatal growth retardation		IEA		N	RGD:5509061	20141003	MGI			
10770	Igf2	insulin-like growth factor 2	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0010970	abnormal compact bone lamellar structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148188
10770	Igf2	insulin-like growth factor 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
10770	Igf2	insulin-like growth factor 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402901
10770	Igf2	insulin-like growth factor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:9389646
10770	Igf2	insulin-like growth factor 2	gene	MP:0012098	increased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
10770	Igf2	insulin-like growth factor 2	gene	MP:0013309	adrenal gland cyst		IAGP		N	RGD:5509061	20141120	MGI			PMID:9389646
10771	Igfbp2	insulin-like growth factor binding protein 2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976924
10771	Igfbp2	insulin-like growth factor binding protein 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
10771	Igfbp2	insulin-like growth factor binding protein 2	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976924
10771	Igfbp2	insulin-like growth factor binding protein 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976924
10771	Igfbp2	insulin-like growth factor binding protein 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976924
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160421	MGI			
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:31526985
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200109	MGI			PMID:31526985
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20250508	MGI			
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20200109	MGI			PMID:31526985
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0008961	abnormal basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0009427	increased tibialis anterior weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0010226	increased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926583
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0010571	shortened ST segment		IEA		N	RGD:5509061	20201022	MGI			
10774	Igfbp3	insulin-like growth factor binding protein 3	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20200109	MGI			PMID:31526985
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10775	Igfbp4	insulin-like growth factor binding protein 4	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10776	Igfbp5	insulin-like growth factor binding protein 5	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675541
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:18925577
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:20458139
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9103198
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:20512127
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20111116	MGI			PMID:20512127
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18925577
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0002606	increased basophil cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:20512127
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:20512127
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:20512127
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:20512127
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:18925577
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:20458139
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9103198
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20111116	MGI			PMID:18354212
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0008728	increased memory B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:18925577
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0010215	abnormal circulating complement protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:20512127
10780	Igh-7	immunoglobulin heavy chain 7 (heavy chain of IgE)	gene	MP:0014471	enhanced B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:18925577
10783	Igkc	immunoglobulin kappa constant	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:16785310
10783	Igkc	immunoglobulin kappa constant	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12538695
10783	Igkc	immunoglobulin kappa constant	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:8458339
10783	Igkc	immunoglobulin kappa constant	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:7664778
10783	Igkc	immunoglobulin kappa constant	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:7664778
10783	Igkc	immunoglobulin kappa constant	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12538695
10783	Igkc	immunoglobulin kappa constant	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20111116	MGI			PMID:8075633
10783	Igkc	immunoglobulin kappa constant	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18086860
10783	Igkc	immunoglobulin kappa constant	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18086860
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20111116	MGI			PMID:18086860
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20111116	MGI			PMID:8235658
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20111116	MGI			PMID:8458339
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:7664778
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:18086860
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12538695
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:7664778
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20130503	MGI			PMID:23296705
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:8075633
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9020839
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20130503	MGI			PMID:23296705
10783	Igkc	immunoglobulin kappa constant	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0003134	increased late pro-B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:8075633
10783	Igkc	immunoglobulin kappa constant	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:9020839
10783	Igkc	immunoglobulin kappa constant	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12538695
10783	Igkc	immunoglobulin kappa constant	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:16785310
10783	Igkc	immunoglobulin kappa constant	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12538695
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20111116	MGI			PMID:12538695
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20111116	MGI			PMID:8075633
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008202	absent B-1 B cells		IAGP		N	RGD:5509061	20111116	MGI			PMID:12538695
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008205	absent B-2 B cells		IAGP		N	RGD:5509061	20111116	MGI			PMID:12538695
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:8075633
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:8458339
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9020839
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:8458339
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20111116	MGI			PMID:12538695
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20111116	MGI			PMID:9020839
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:8458339
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20111116	MGI			PMID:18086860
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20111116	MGI			PMID:9020839
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008761	abnormal immunoglobulin light chain V-J recombination		IAGP		N	RGD:5509061	20111116	MGI			PMID:19116268
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008761	abnormal immunoglobulin light chain V-J recombination		IAGP		N	RGD:5509061	20111116	MGI			PMID:9020839
10783	Igkc	immunoglobulin kappa constant	gene	MP:0008761	abnormal immunoglobulin light chain V-J recombination		IAGP		N	RGD:5509061	20111116	MGI			PMID:9687526
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12538695
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12538695
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18086860
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18086860
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18086860
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18086860
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12538695
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12538695
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12538695
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0008202	absent B-1 B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12538695
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0008205	absent B-2 B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12538695
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12538695
10784	Igl	immunoglobulin lambda chain complex	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18086860
10785	Il10	interleukin 10	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765335
10785	Il10	interleukin 10	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765335
10785	Il10	interleukin 10	gene	MP:0000199	abnormal circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0000216	absent erythroid progenitor cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617560
10785	Il10	interleukin 10	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:24442434
10785	Il10	interleukin 10	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
10785	Il10	interleukin 10	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285204
10785	Il10	interleukin 10	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20170126	MGI			
10785	Il10	interleukin 10	gene	MP:0000880	decreased Purkinje cell number		IEA		N	RGD:5509061	20170126	MGI			
10785	Il10	interleukin 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579119
10785	Il10	interleukin 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12823276
10785	Il10	interleukin 10	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859330
10785	Il10	interleukin 10	gene	MP:0001393	ataxia		IEA		N	RGD:5509061	20170126	MGI			
10785	Il10	interleukin 10	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650318
10785	Il10	interleukin 10	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11353686
10785	Il10	interleukin 10	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497487
10785	Il10	interleukin 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
10785	Il10	interleukin 10	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859330
10785	Il10	interleukin 10	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17111348
10785	Il10	interleukin 10	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003481
10785	Il10	interleukin 10	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015721
10785	Il10	interleukin 10	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
10785	Il10	interleukin 10	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18026113
10785	Il10	interleukin 10	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:12799032
10785	Il10	interleukin 10	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17579057
10785	Il10	interleukin 10	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
10785	Il10	interleukin 10	gene	MP:0002148	abnormal hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137799
10785	Il10	interleukin 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844394
10785	Il10	interleukin 10	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811896
10785	Il10	interleukin 10	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15618456
10785	Il10	interleukin 10	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832734
10785	Il10	interleukin 10	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811896
10785	Il10	interleukin 10	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0002534	abnormal type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
10785	Il10	interleukin 10	gene	MP:0002534	abnormal type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823360
10785	Il10	interleukin 10	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765335
10785	Il10	interleukin 10	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200193
10785	Il10	interleukin 10	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579119
10785	Il10	interleukin 10	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285204
10785	Il10	interleukin 10	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12823276
10785	Il10	interleukin 10	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
10785	Il10	interleukin 10	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
10785	Il10	interleukin 10	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24442434
10785	Il10	interleukin 10	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
10785	Il10	interleukin 10	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285204
10785	Il10	interleukin 10	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17111348
10785	Il10	interleukin 10	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074677
10785	Il10	interleukin 10	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10512928
10785	Il10	interleukin 10	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406467
10785	Il10	interleukin 10	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617560
10785	Il10	interleukin 10	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0003434	decreased susceptibility to induced choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16903779
10785	Il10	interleukin 10	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497487
10785	Il10	interleukin 10	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15618456
10785	Il10	interleukin 10	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0004504	decreased incidence of tumors by UV induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17579057
10785	Il10	interleukin 10	gene	MP:0004752	decreased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:9366559
10785	Il10	interleukin 10	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832734
10785	Il10	interleukin 10	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10947805
10785	Il10	interleukin 10	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074677
10785	Il10	interleukin 10	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391195
10785	Il10	interleukin 10	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
10785	Il10	interleukin 10	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600128
10785	Il10	interleukin 10	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:24442434
10785	Il10	interleukin 10	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0005046	absent spleen white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17579057
10785	Il10	interleukin 10	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765335
10785	Il10	interleukin 10	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765335
10785	Il10	interleukin 10	gene	MP:0005362	abnormal Langerhans cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886396
10785	Il10	interleukin 10	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497487
10785	Il10	interleukin 10	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
10785	Il10	interleukin 10	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
10785	Il10	interleukin 10	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886396
10785	Il10	interleukin 10	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10947805
10785	Il10	interleukin 10	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
10785	Il10	interleukin 10	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
10785	Il10	interleukin 10	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0008121	increased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10947805
10785	Il10	interleukin 10	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0008387	hypochromic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574631
10785	Il10	interleukin 10	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811896
10785	Il10	interleukin 10	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811896
10785	Il10	interleukin 10	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
10785	Il10	interleukin 10	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380512
10785	Il10	interleukin 10	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
10785	Il10	interleukin 10	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
10785	Il10	interleukin 10	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
10785	Il10	interleukin 10	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765335
10785	Il10	interleukin 10	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0008595	abnormal circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23241891
10785	Il10	interleukin 10	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650318
10785	Il10	interleukin 10	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008599	increased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765335
10785	Il10	interleukin 10	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380512
10785	Il10	interleukin 10	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008638	increased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650318
10785	Il10	interleukin 10	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008646	abnormal circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23241891
10785	Il10	interleukin 10	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
10785	Il10	interleukin 10	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
10785	Il10	interleukin 10	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21460847
10785	Il10	interleukin 10	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24442434
10785	Il10	interleukin 10	gene	MP:0008666	increased interleukin-12a secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
10785	Il10	interleukin 10	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
10785	Il10	interleukin 10	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
10785	Il10	interleukin 10	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
10785	Il10	interleukin 10	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
10785	Il10	interleukin 10	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650318
10785	Il10	interleukin 10	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380512
10785	Il10	interleukin 10	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:17111348
10785	Il10	interleukin 10	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
10785	Il10	interleukin 10	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17579057
10785	Il10	interleukin 10	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886396
10785	Il10	interleukin 10	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886396
10785	Il10	interleukin 10	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842419
10785	Il10	interleukin 10	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402911
10785	Il10	interleukin 10	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15618456
10785	Il10	interleukin 10	gene	MP:0009310	increased large intestine adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0009314	increased colon adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617560
10785	Il10	interleukin 10	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709607
10785	Il10	interleukin 10	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941312
10785	Il10	interleukin 10	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8770874
10785	Il10	interleukin 10	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
10785	Il10	interleukin 10	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15534372
10785	Il10	interleukin 10	gene	MP:0009816	increased leukotriene level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811896
10785	Il10	interleukin 10	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579119
10785	Il10	interleukin 10	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765335
10785	Il10	interleukin 10	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
10785	Il10	interleukin 10	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0010962	decreased compact bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15362035
10785	Il10	interleukin 10	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11353686
10785	Il10	interleukin 10	gene	MP:0011520	increased placental labyrinth size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842419
10785	Il10	interleukin 10	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650318
10785	Il10	interleukin 10	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160304	MGI			PMID:24442434
10785	Il10	interleukin 10	gene	MP:0030466	alveolar process atrophy		IAGP		N	RGD:5509061	20171221	MGI			PMID:17305866
10785	Il10	interleukin 10	gene	MP:0031157	abnormal arterial thrombosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:12765335
10785	Il10	interleukin 10	gene	MP:0031698	decreased bone marrow iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:8402911
10786	Il15	interleukin 15	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20200402	MGI			
10786	Il15	interleukin 15	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704459
10786	Il15	interleukin 15	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12816981
10786	Il15	interleukin 15	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20160421	MGI			
10786	Il15	interleukin 15	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704459
10786	Il15	interleukin 15	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704459
10786	Il15	interleukin 15	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845528
10786	Il15	interleukin 15	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845528
10786	Il15	interleukin 15	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704459
10786	Il15	interleukin 15	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16020505
10786	Il15	interleukin 15	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845528
10786	Il15	interleukin 15	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704459
10786	Il15	interleukin 15	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845528
10786	Il15	interleukin 15	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12816981
10786	Il15	interleukin 15	gene	MP:0003995	abnormal uterine artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12816981
10786	Il15	interleukin 15	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630141
10786	Il15	interleukin 15	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23805138
10786	Il15	interleukin 15	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845528
10786	Il15	interleukin 15	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845528
10786	Il15	interleukin 15	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
10786	Il15	interleukin 15	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14635060
10786	Il15	interleukin 15	gene	MP:0008038	abnormal NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22346732
10786	Il15	interleukin 15	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22346732
10786	Il15	interleukin 15	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704459
10786	Il15	interleukin 15	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12586624
10786	Il15	interleukin 15	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449532
10786	Il15	interleukin 15	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19084435
10786	Il15	interleukin 15	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22346732
10786	Il15	interleukin 15	gene	MP:0008047	absent uterine NK cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12816981
10786	Il15	interleukin 15	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449532
10786	Il15	interleukin 15	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20151231	MGI			PMID:24516120
10786	Il15	interleukin 15	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704459
10786	Il15	interleukin 15	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
10786	Il15	interleukin 15	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880398
10786	Il15	interleukin 15	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109710
10786	Il15	interleukin 15	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880398
10786	Il15	interleukin 15	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845528
10786	Il15	interleukin 15	gene	MP:0008363	decreased CD8-positive, gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913445
10786	Il15	interleukin 15	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845528
10786	Il15	interleukin 15	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22346732
10786	Il15	interleukin 15	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22346732
10786	Il15	interleukin 15	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845528
10786	Il15	interleukin 15	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880398
10786	Il15	interleukin 15	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12816981
10786	Il15	interleukin 15	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:21964024
10786	Il15	interleukin 15	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:15767447
10786	Il15	interleukin 15	gene	MP:0031034	increased susceptibility to Poxviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:10704459
10787	Il17a	interleukin 17A	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
10787	Il17a	interleukin 17A	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
10787	Il17a	interleukin 17A	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
10787	Il17a	interleukin 17A	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20161110	MGI			PMID:25411202
10787	Il17a	interleukin 17A	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
10787	Il17a	interleukin 17A	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
10787	Il17a	interleukin 17A	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
10787	Il17a	interleukin 17A	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075395
10787	Il17a	interleukin 17A	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354389
10787	Il17a	interleukin 17A	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
10787	Il17a	interleukin 17A	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0001866	nasal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
10787	Il17a	interleukin 17A	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20200730	MGI			PMID:29980436
10787	Il17a	interleukin 17A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
10787	Il17a	interleukin 17A	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
10787	Il17a	interleukin 17A	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
10787	Il17a	interleukin 17A	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354389
10787	Il17a	interleukin 17A	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354389
10787	Il17a	interleukin 17A	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
10787	Il17a	interleukin 17A	gene	MP:0002742	enlarged submandibular lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
10787	Il17a	interleukin 17A	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
10787	Il17a	interleukin 17A	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12721360
10787	Il17a	interleukin 17A	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
10787	Il17a	interleukin 17A	gene	MP:0003747	mouth mucosal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
10787	Il17a	interleukin 17A	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
10787	Il17a	interleukin 17A	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
10787	Il17a	interleukin 17A	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20161110	MGI			PMID:25411202
10787	Il17a	interleukin 17A	gene	MP:0005362	abnormal Langerhans cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354389
10787	Il17a	interleukin 17A	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354389
10787	Il17a	interleukin 17A	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
10787	Il17a	interleukin 17A	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
10787	Il17a	interleukin 17A	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
10787	Il17a	interleukin 17A	gene	MP:0008348	absent gamma-delta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
10787	Il17a	interleukin 17A	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354389
10787	Il17a	interleukin 17A	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
10787	Il17a	interleukin 17A	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
10787	Il17a	interleukin 17A	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
10787	Il17a	interleukin 17A	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
10787	Il17a	interleukin 17A	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
10787	Il17a	interleukin 17A	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
10787	Il17a	interleukin 17A	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
10787	Il17a	interleukin 17A	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
10787	Il17a	interleukin 17A	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354389
10787	Il17a	interleukin 17A	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
10787	Il17a	interleukin 17A	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
10787	Il17a	interleukin 17A	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354389
10787	Il17a	interleukin 17A	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
10787	Il17a	interleukin 17A	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919941
10787	Il17a	interleukin 17A	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
10787	Il17a	interleukin 17A	gene	MP:0009787	increased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493731
10787	Il17a	interleukin 17A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200723	MGI			PMID:29980436
10787	Il17a	interleukin 17A	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
10789	Il1a	interleukin 1 alpha	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
10789	Il1a	interleukin 1 alpha	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23219391
10789	Il1a	interleukin 1 alpha	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151598
10789	Il1a	interleukin 1 alpha	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12598651
10789	Il1a	interleukin 1 alpha	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
10789	Il1a	interleukin 1 alpha	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
10789	Il1a	interleukin 1 alpha	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23219391
10789	Il1a	interleukin 1 alpha	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9565638
10789	Il1a	interleukin 1 alpha	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
10789	Il1a	interleukin 1 alpha	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
10789	Il1a	interleukin 1 alpha	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9565638
10789	Il1a	interleukin 1 alpha	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
10789	Il1a	interleukin 1 alpha	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
10789	Il1a	interleukin 1 alpha	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
10789	Il1a	interleukin 1 alpha	gene	MP:0008639	decreased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9565638
10789	Il1a	interleukin 1 alpha	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9565638
10789	Il1a	interleukin 1 alpha	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9565638
10789	Il1a	interleukin 1 alpha	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9809553
10789	Il1a	interleukin 1 alpha	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12598651
10790	Il1b	interleukin 1 beta	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20180719	MGI			PMID:11549714
10790	Il1b	interleukin 1 beta	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11549714
10790	Il1b	interleukin 1 beta	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:12151598
10790	Il1b	interleukin 1 beta	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20180719	MGI			PMID:10639148
10790	Il1b	interleukin 1 beta	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20180719	MGI			PMID:12598651
10790	Il1b	interleukin 1 beta	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:7621081
10790	Il1b	interleukin 1 beta	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:18194440
10790	Il1b	interleukin 1 beta	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:16861683
10790	Il1b	interleukin 1 beta	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18493980
10790	Il1b	interleukin 1 beta	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9565638
10790	Il1b	interleukin 1 beta	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20180719	MGI			PMID:10639148
10790	Il1b	interleukin 1 beta	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20180719	MGI			PMID:12598651
10790	Il1b	interleukin 1 beta	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20180719	MGI			PMID:7621081
10790	Il1b	interleukin 1 beta	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20180719	MGI			PMID:9565638
10790	Il1b	interleukin 1 beta	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11265638
10790	Il1b	interleukin 1 beta	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:20937871
10790	Il1b	interleukin 1 beta	gene	MP:0004824	decreased susceptibility to experimental autoimmune myasthenia gravis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11265638
10790	Il1b	interleukin 1 beta	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20180719	MGI			PMID:16565512
10790	Il1b	interleukin 1 beta	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:7621081
10790	Il1b	interleukin 1 beta	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180719	MGI			PMID:11589427
10790	Il1b	interleukin 1 beta	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180719	MGI			PMID:16439700
10790	Il1b	interleukin 1 beta	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20180719	MGI			PMID:11589427
10790	Il1b	interleukin 1 beta	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20180719	MGI			PMID:20937871
10790	Il1b	interleukin 1 beta	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20180719	MGI			PMID:8666901
10790	Il1b	interleukin 1 beta	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:12598651
10790	Il1b	interleukin 1 beta	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11265638
10790	Il1b	interleukin 1 beta	gene	MP:0008639	decreased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9565638
10790	Il1b	interleukin 1 beta	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7621081
10790	Il1b	interleukin 1 beta	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9565638
10790	Il1b	interleukin 1 beta	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:18493980
10790	Il1b	interleukin 1 beta	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:8666901
10790	Il1b	interleukin 1 beta	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11265638
10790	Il1b	interleukin 1 beta	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11265638
10790	Il1b	interleukin 1 beta	gene	MP:0008704	abnormal interleukin-6 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:7621081
10790	Il1b	interleukin 1 beta	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20180719	MGI			PMID:9809553
10790	Il1b	interleukin 1 beta	gene	MP:0008831	abnormal insulin-like growth factor I level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11549714
10790	Il1b	interleukin 1 beta	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:10639148
10790	Il1b	interleukin 1 beta	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:11265638
10790	Il1b	interleukin 1 beta	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:12598651
10790	Il1b	interleukin 1 beta	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:18493980
10790	Il1b	interleukin 1 beta	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20180719	MGI			PMID:12598651
10790	Il1b	interleukin 1 beta	gene	MP:0020941	decreased susceptibility to Togaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:9971844
10790	Il1b	interleukin 1 beta	gene	MP:0030524	abnormal tooth root resorption		IAGP		N	RGD:5509061	20180719	MGI			PMID:15758271
10790	Il1b	interleukin 1 beta	gene	MP:0031041	decreased susceptibility to Togaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:9971844
10791	Il1rap	interleukin 1 receptor accessory protein	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
10791	Il1rap	interleukin 1 receptor accessory protein	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820540
10796	Il4	interleukin 4	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17913905
10796	Il4	interleukin 4	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20180719	MGI			PMID:16547221
10796	Il4	interleukin 4	gene	MP:0000324	increased mast cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0000466	esophageal epithelium hyperplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0000701	abnormal lymph node size		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330435
10796	Il4	interleukin 4	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:10679097
10796	Il4	interleukin 4	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10796	Il4	interleukin 4	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:18250447
10796	Il4	interleukin 4	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330435
10796	Il4	interleukin 4	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330435
10796	Il4	interleukin 4	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7517363
10796	Il4	interleukin 4	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7609051
10796	Il4	interleukin 4	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446913
10796	Il4	interleukin 4	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446913
10796	Il4	interleukin 4	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20180719	MGI			PMID:9703318
10796	Il4	interleukin 4	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11342667
10796	Il4	interleukin 4	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:16413168
10796	Il4	interleukin 4	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:10878379
10796	Il4	interleukin 4	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:10679097
10796	Il4	interleukin 4	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:20937871
10796	Il4	interleukin 4	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20180719	MGI			PMID:10486156
10796	Il4	interleukin 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12709397
10796	Il4	interleukin 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:10069422
10796	Il4	interleukin 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:16226507
10796	Il4	interleukin 4	gene	MP:0002224	abnormal spleen size		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20180719	MGI			PMID:21131966
10796	Il4	interleukin 4	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150890
10796	Il4	interleukin 4	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:17182558
10796	Il4	interleukin 4	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446913
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11591797
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11745342
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:18719110
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:1948049
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:21131966
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:22138715
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:22326582
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7598937
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8384701
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8584936
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8384701
10796	Il4	interleukin 4	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10796	Il4	interleukin 4	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0002606	increased basophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0002607	decreased basophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22326582
10796	Il4	interleukin 4	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20180719	MGI			PMID:18055812
10796	Il4	interleukin 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11342667
10796	Il4	interleukin 4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:16547221
10796	Il4	interleukin 4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:1948049
10796	Il4	interleukin 4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:9703318
10796	Il4	interleukin 4	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7517363
10796	Il4	interleukin 4	gene	MP:0003278	esophageal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10796	Il4	interleukin 4	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9703318
10796	Il4	interleukin 4	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0004795	decreased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20180719	MGI			PMID:9703318
10796	Il4	interleukin 4	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10796	Il4	interleukin 4	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22138715
10796	Il4	interleukin 4	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7598937
10796	Il4	interleukin 4	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:16547221
10796	Il4	interleukin 4	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:8384701
10796	Il4	interleukin 4	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:11745342
10796	Il4	interleukin 4	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330435
10796	Il4	interleukin 4	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:10679097
10796	Il4	interleukin 4	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10796	Il4	interleukin 4	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:22138715
10796	Il4	interleukin 4	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20180719	MGI			PMID:7609051
10796	Il4	interleukin 4	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:7517363
10796	Il4	interleukin 4	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180719	MGI			PMID:15034018
10796	Il4	interleukin 4	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20180719	MGI			PMID:22101429
10796	Il4	interleukin 4	gene	MP:0005310	abnormal salivary gland physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16413168
10796	Il4	interleukin 4	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:7517363
10796	Il4	interleukin 4	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20180719	MGI			PMID:15613333
10796	Il4	interleukin 4	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20180719	MGI			PMID:11591797
10796	Il4	interleukin 4	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20180719	MGI			PMID:15613333
10796	Il4	interleukin 4	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20180719	MGI			PMID:17182558
10796	Il4	interleukin 4	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330435
10796	Il4	interleukin 4	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150890
10796	Il4	interleukin 4	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16547221
10796	Il4	interleukin 4	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19682930
10796	Il4	interleukin 4	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20147633
10796	Il4	interleukin 4	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20180719	MGI			PMID:15613333
10796	Il4	interleukin 4	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:16413168
10796	Il4	interleukin 4	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:17913905
10796	Il4	interleukin 4	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20180719	MGI			PMID:17611223
10796	Il4	interleukin 4	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:16778988
10796	Il4	interleukin 4	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:18719110
10796	Il4	interleukin 4	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:17182558
10796	Il4	interleukin 4	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7517363
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11745342
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446913
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:1948049
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:21131966
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:22138715
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:22326582
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8384701
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8584936
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9647229
10796	Il4	interleukin 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9703318
10796	Il4	interleukin 4	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446913
10796	Il4	interleukin 4	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446913
10796	Il4	interleukin 4	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446913
10796	Il4	interleukin 4	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9109438
10796	Il4	interleukin 4	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20180719	MGI			PMID:11591797
10796	Il4	interleukin 4	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9647229
10796	Il4	interleukin 4	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446913
10796	Il4	interleukin 4	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:10878379
10796	Il4	interleukin 4	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:16778988
10796	Il4	interleukin 4	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:17182558
10796	Il4	interleukin 4	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11591797
10796	Il4	interleukin 4	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:10878379
10796	Il4	interleukin 4	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:8384701
10796	Il4	interleukin 4	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:21131966
10796	Il4	interleukin 4	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11591797
10796	Il4	interleukin 4	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150890
10796	Il4	interleukin 4	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:17182558
10796	Il4	interleukin 4	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0008697	decreased interleukin-3 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:8384701
10796	Il4	interleukin 4	gene	MP:0008698	abnormal interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11591797
10796	Il4	interleukin 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:10486156
10796	Il4	interleukin 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11163225
10796	Il4	interleukin 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11323701
10796	Il4	interleukin 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150890
10796	Il4	interleukin 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:21131966
10796	Il4	interleukin 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:22326582
10796	Il4	interleukin 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:8384701
10796	Il4	interleukin 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:21131966
10796	Il4	interleukin 4	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11591797
10796	Il4	interleukin 4	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:17182558
10796	Il4	interleukin 4	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:7598937
10796	Il4	interleukin 4	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:8384701
10796	Il4	interleukin 4	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:8906833
10796	Il4	interleukin 4	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20180719	MGI			PMID:18719110
10796	Il4	interleukin 4	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20180719	MGI			PMID:21131966
10796	Il4	interleukin 4	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20180719	MGI			PMID:9647229
10796	Il4	interleukin 4	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:16413168
10796	Il4	interleukin 4	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:18055812
10796	Il4	interleukin 4	gene	MP:0008896	increased IgG2c level		IAGP		N	RGD:5509061	20180719	MGI			PMID:21131966
10796	Il4	interleukin 4	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10679097
10796	Il4	interleukin 4	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11745342
10796	Il4	interleukin 4	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:10679097
10796	Il4	interleukin 4	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20180719	MGI			PMID:22101429
10796	Il4	interleukin 4	gene	MP:0010215	abnormal circulating complement protein level		IAGP		N	RGD:5509061	20180719	MGI			PMID:20512127
10796	Il4	interleukin 4	gene	MP:0010750	increased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:10679097
10796	Il4	interleukin 4	gene	MP:0010945	lung epithelium hyperplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:23851689
10796	Il4	interleukin 4	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20180719	MGI			PMID:22101429
10796	Il4	interleukin 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:11342667
10796	Il4	interleukin 4	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:22101429
10796	Il4	interleukin 4	gene	MP:0014981	increased amylase activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:16413168
10796	Il4	interleukin 4	gene	MP:0020912	abnormal susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:7609051
10796	Il4	interleukin 4	gene	MP:0030466	alveolar process atrophy		IAGP		N	RGD:5509061	20180719	MGI			PMID:17305866
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17913905
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18220315
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18220315
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11168809
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11168809
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10358179
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250447
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557412
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557412
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002434	abnormal T-helper 2 cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557412
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380721
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557412
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557412
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392476
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557412
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11168809
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142530
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9492006
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557412
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101429
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380721
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392476
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109710
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008091	decreased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21460847
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11168809
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380721
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380721
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9492006
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008551	abnormal circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18220315
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18220315
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380721
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392476
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380721
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380721
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0008837	increased transforming growth factor beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18220315
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18220315
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0010861	increased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770271
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101429
10798	Il4ra	interleukin 4 receptor, alpha	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392476
10799	Il5	interleukin 5	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8551223
10799	Il5	interleukin 5	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:11058459
10799	Il5	interleukin 5	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20180719	MGI			PMID:22174445
10799	Il5	interleukin 5	gene	MP:0001376	abnormal mating receptivity		IAGP		N	RGD:5509061	20180719	MGI			PMID:11058459
10799	Il5	interleukin 5	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:24037376
10799	Il5	interleukin 5	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20180719	MGI			PMID:8551223
10799	Il5	interleukin 5	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:16495517
10799	Il5	interleukin 5	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:16495517
10799	Il5	interleukin 5	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20180719	MGI			PMID:11058459
10799	Il5	interleukin 5	gene	MP:0004940	abnormal B-1 B cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:22174445
10799	Il5	interleukin 5	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8574848
10799	Il5	interleukin 5	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8551223
10799	Il5	interleukin 5	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:16495517
10799	Il5	interleukin 5	gene	MP:0008627	decreased circulating interleukin-5 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:24037376
10799	Il5	interleukin 5	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:22174445
10799	Il5	interleukin 5	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12150887
10799	Il5	interleukin 5	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20180719	MGI			PMID:11058459
10802	Il6	interleukin 6	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17921078
10802	Il6	interleukin 6	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018077
10802	Il6	interleukin 6	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8131749
10802	Il6	interleukin 6	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8131749
10802	Il6	interleukin 6	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223557
10802	Il6	interleukin 6	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12957371
10802	Il6	interleukin 6	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:23085146
10802	Il6	interleukin 6	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8910279
10802	Il6	interleukin 6	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9169772
10802	Il6	interleukin 6	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
10802	Il6	interleukin 6	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
10802	Il6	interleukin 6	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223557
10802	Il6	interleukin 6	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19918056
10802	Il6	interleukin 6	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19918056
10802	Il6	interleukin 6	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11006436
10802	Il6	interleukin 6	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23085146
10802	Il6	interleukin 6	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988384
10802	Il6	interleukin 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988384
10802	Il6	interleukin 6	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:9875345
10802	Il6	interleukin 6	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11006436
10802	Il6	interleukin 6	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9875345
10802	Il6	interleukin 6	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12946594
10802	Il6	interleukin 6	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16843000
10802	Il6	interleukin 6	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378383
10802	Il6	interleukin 6	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11006436
10802	Il6	interleukin 6	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23085146
10802	Il6	interleukin 6	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378383
10802	Il6	interleukin 6	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436757
10802	Il6	interleukin 6	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265638
10802	Il6	interleukin 6	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378383
10802	Il6	interleukin 6	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581736
10802	Il6	interleukin 6	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367337
10802	Il6	interleukin 6	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018077
10802	Il6	interleukin 6	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8131749
10802	Il6	interleukin 6	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831701
10802	Il6	interleukin 6	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17615358
10802	Il6	interleukin 6	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8910279
10802	Il6	interleukin 6	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988384
10802	Il6	interleukin 6	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11006436
10802	Il6	interleukin 6	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20483735
10802	Il6	interleukin 6	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12957371
10802	Il6	interleukin 6	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20483735
10802	Il6	interleukin 6	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
10802	Il6	interleukin 6	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9169772
10802	Il6	interleukin 6	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11208530
10802	Il6	interleukin 6	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284817
10802	Il6	interleukin 6	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12358740
10802	Il6	interleukin 6	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215902
10802	Il6	interleukin 6	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056981
10802	Il6	interleukin 6	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284817
10802	Il6	interleukin 6	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265638
10802	Il6	interleukin 6	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378383
10802	Il6	interleukin 6	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
10802	Il6	interleukin 6	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581004
10802	Il6	interleukin 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
10802	Il6	interleukin 6	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8127368
10802	Il6	interleukin 6	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223557
10802	Il6	interleukin 6	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
10802	Il6	interleukin 6	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12957371
10802	Il6	interleukin 6	gene	MP:0002332	abnormal exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988384
10802	Il6	interleukin 6	gene	MP:0002336	abnormal pulmonary gas exchange		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988384
10802	Il6	interleukin 6	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831701
10802	Il6	interleukin 6	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7768607
10802	Il6	interleukin 6	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8127368
10802	Il6	interleukin 6	gene	MP:0002433	abnormal T-helper 1 cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18504307
10802	Il6	interleukin 6	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20083667
10802	Il6	interleukin 6	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7768607
10802	Il6	interleukin 6	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16843000
10802	Il6	interleukin 6	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378383
10802	Il6	interleukin 6	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23085146
10802	Il6	interleukin 6	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16843000
10802	Il6	interleukin 6	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378383
10802	Il6	interleukin 6	gene	MP:0002711	decreased glucagon secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719127
10802	Il6	interleukin 6	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215902
10802	Il6	interleukin 6	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265638
10802	Il6	interleukin 6	gene	MP:0002801	abnormal long-term object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436757
10802	Il6	interleukin 6	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223557
10802	Il6	interleukin 6	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20483735
10802	Il6	interleukin 6	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:8131749
10802	Il6	interleukin 6	gene	MP:0002999	abnormal bone healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17921078
10802	Il6	interleukin 6	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719127
10802	Il6	interleukin 6	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177723
10802	Il6	interleukin 6	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17615358
10802	Il6	interleukin 6	gene	MP:0003194	abnormal frequency of paradoxical sleep		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581736
10802	Il6	interleukin 6	gene	MP:0003278	esophageal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22264787
10802	Il6	interleukin 6	gene	MP:0003326	liver failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8910279
10802	Il6	interleukin 6	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
10802	Il6	interleukin 6	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
10802	Il6	interleukin 6	gene	MP:0003459	increased fear-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16843000
10802	Il6	interleukin 6	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436757
10802	Il6	interleukin 6	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712626
10802	Il6	interleukin 6	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314284
10802	Il6	interleukin 6	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12957371
10802	Il6	interleukin 6	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
10802	Il6	interleukin 6	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8551238
10802	Il6	interleukin 6	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9688988
10802	Il6	interleukin 6	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436757
10802	Il6	interleukin 6	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17615358
10802	Il6	interleukin 6	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
10802	Il6	interleukin 6	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831701
10802	Il6	interleukin 6	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436757
10802	Il6	interleukin 6	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11006436
10802	Il6	interleukin 6	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19918056
10802	Il6	interleukin 6	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
10802	Il6	interleukin 6	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8127368
10802	Il6	interleukin 6	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20483735
10802	Il6	interleukin 6	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9169772
10802	Il6	interleukin 6	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8127368
10802	Il6	interleukin 6	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284817
10802	Il6	interleukin 6	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712626
10802	Il6	interleukin 6	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:11208530
10802	Il6	interleukin 6	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18423196
10802	Il6	interleukin 6	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
10802	Il6	interleukin 6	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988384
10802	Il6	interleukin 6	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719127
10802	Il6	interleukin 6	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223557
10802	Il6	interleukin 6	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9688988
10802	Il6	interleukin 6	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8910279
10802	Il6	interleukin 6	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581736
10802	Il6	interleukin 6	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367337
10802	Il6	interleukin 6	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988384
10802	Il6	interleukin 6	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
10802	Il6	interleukin 6	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9875345
10802	Il6	interleukin 6	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12456808
10802	Il6	interleukin 6	gene	MP:0008046	absent NK cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9169772
10802	Il6	interleukin 6	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
10802	Il6	interleukin 6	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831701
10802	Il6	interleukin 6	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018077
10802	Il6	interleukin 6	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018077
10802	Il6	interleukin 6	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378582
10802	Il6	interleukin 6	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12219085
10802	Il6	interleukin 6	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581589
10802	Il6	interleukin 6	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
10802	Il6	interleukin 6	gene	MP:0008618	decreased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666893
10802	Il6	interleukin 6	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
10802	Il6	interleukin 6	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20083667
10802	Il6	interleukin 6	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581589
10802	Il6	interleukin 6	gene	MP:0008704	abnormal interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581004
10802	Il6	interleukin 6	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11208530
10802	Il6	interleukin 6	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148800
10802	Il6	interleukin 6	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9169772
10802	Il6	interleukin 6	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
10802	Il6	interleukin 6	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23085146
10802	Il6	interleukin 6	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177723
10802	Il6	interleukin 6	gene	MP:0009753	enhanced behavioral response to morphine		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215902
10802	Il6	interleukin 6	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8910279
10802	Il6	interleukin 6	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9688988
10802	Il6	interleukin 6	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264109
10802	Il6	interleukin 6	gene	MP:0009978	abnormal cerebellum white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
10802	Il6	interleukin 6	gene	MP:0010042	abnormal oval cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120777
10802	Il6	interleukin 6	gene	MP:0010119	abnormal bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018077
10802	Il6	interleukin 6	gene	MP:0010211	abnormal acute phase protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8127368
10802	Il6	interleukin 6	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
10802	Il6	interleukin 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23085146
10802	Il6	interleukin 6	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12358740
10802	Il6	interleukin 6	gene	MP:0012563	increased tumor incidence following infection		IAGP		N	RGD:5509061	20241114	MGI			PMID:36103821
10802	Il6	interleukin 6	gene	MP:0013219	abnormal substantia nigra pars compacta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12358740
10802	Il6	interleukin 6	gene	MP:0014190	abnormal epididymis physiology		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
10802	Il6	interleukin 6	gene	MP:0014315	decreased heart left ventricle anterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:19378383
10802	Il6	interleukin 6	gene	MP:0020340	abnormal inhibitory learning		IAGP		N	RGD:5509061	20160915	MGI			PMID:19378383
10802	Il6	interleukin 6	gene	MP:0020928	increased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:8127368
10802	Il6	interleukin 6	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:19234091
10802	Il6	interleukin 6	gene	MP:0030587	abnormal pancreatic alpha cell mass		IAGP		N	RGD:5509061	20180614	MGI			PMID:18719127
10802	Il6	interleukin 6	gene	MP:0030945	abnormal myoblast migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:18177723
10802	Il6	interleukin 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12946594
10802	Il6	interleukin 6	gene	MP:0031425	enhanced male fertility		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
10802	Il6	interleukin 6	gene	MP:0031426	increased sperm motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
10802	Il6	interleukin 6	gene	MP:0031427	increased sperm progressive motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:23085146
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378927
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378927
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20483735
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23954788
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20483735
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23085146
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0002714	increased glycogen catabolism rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816090
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816090
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816090
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23954788
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23954788
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23954788
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23954788
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378927
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20483735
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467660
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20483735
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816090
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816090
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23954788
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816090
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20083667
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20260402	MGI			
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378927
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378927
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816090
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467660
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816090
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467660
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20241121	MGI			
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0010214	abnormal circulating serum amyloid protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378927
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816090
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467660
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23085146
10803	Il6ra	interleukin 6 receptor, alpha	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:20816090
10804	Kpnb1	karyopherin subunit beta 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16414015
10804	Kpnb1	karyopherin subunit beta 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20151112	MGI			PMID:22841314
10804	Kpnb1	karyopherin subunit beta 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16414015
10806	Ina	internexin neuronal intermediate filament protein, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10350642
10806	Ina	internexin neuronal intermediate filament protein, alpha	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:17005864
10808	Inha	inhibin alpha	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0001123	dilated uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895659
10808	Inha	inhibin alpha	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10808	Inha	inhibin alpha	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652186
10808	Inha	inhibin alpha	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1448148
10808	Inha	inhibin alpha	gene	MP:0001148	enlarged testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1448148
10808	Inha	inhibin alpha	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1448148
10808	Inha	inhibin alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1448148
10808	Inha	inhibin alpha	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10808	Inha	inhibin alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1448148
10808	Inha	inhibin alpha	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1448148
10808	Inha	inhibin alpha	gene	MP:0001934	increased litter size		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10808	Inha	inhibin alpha	gene	MP:0001939	secondary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895659
10808	Inha	inhibin alpha	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895659
10808	Inha	inhibin alpha	gene	MP:0002031	increased adrenal gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652186
10808	Inha	inhibin alpha	gene	MP:0002031	increased adrenal gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8828479
10808	Inha	inhibin alpha	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0002776	increased Sertoli cell number		IAGP		N	RGD:5509061	20220630	MGI			PMID:17652186
10808	Inha	inhibin alpha	gene	MP:0002789	male pseudohermaphroditism		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895659
10808	Inha	inhibin alpha	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10808	Inha	inhibin alpha	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:1448148
10808	Inha	inhibin alpha	gene	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652186
10808	Inha	inhibin alpha	gene	MP:0004855	increased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652186
10808	Inha	inhibin alpha	gene	MP:0004855	increased ovary weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10808	Inha	inhibin alpha	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10808	Inha	inhibin alpha	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0005151	diffuse hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652186
10808	Inha	inhibin alpha	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895659
10808	Inha	inhibin alpha	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1448148
10808	Inha	inhibin alpha	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652186
10808	Inha	inhibin alpha	gene	MP:0009257	dilated seminiferous tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0009590	increased gonad tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1448148
10808	Inha	inhibin alpha	gene	MP:0009592	increased Leydig cell tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895659
10808	Inha	inhibin alpha	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855748
10808	Inha	inhibin alpha	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0011124	increased primary ovarian follicle number		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10808	Inha	inhibin alpha	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8895659
10808	Inha	inhibin alpha	gene	MP:0031301	chronic liver inflammation		IAGP		N	RGD:5509061	20211028	MGI			PMID:8090730
10808	Inha	inhibin alpha	gene	MP:0031407	increased Sertoli cell proliferation		IAGP		N	RGD:5509061	20220630	MGI			PMID:17652186
10808	Inha	inhibin alpha	gene	MP:0031411	increased ovulation rate		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10808	Inha	inhibin alpha	gene	MP:0031421	increased superovulation rate		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10808	Inha	inhibin alpha	gene	MP:0031424	enhanced female fertility		IAGP		N	RGD:5509061	20230629	MGI			PMID:35255139
10810	Inhbb	inhibin beta-B	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885473
10810	Inhbb	inhibin beta-B	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885473
10810	Inhbb	inhibin beta-B	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885473
10810	Inhbb	inhibin beta-B	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7947320
10810	Inhbb	inhibin beta-B	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:7947320
10810	Inhbb	inhibin beta-B	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:7947320
10810	Inhbb	inhibin beta-B	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20210128	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20210128	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20210128	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0002293	long gestation period		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0002681	increased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0003153	early eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:7947320
10810	Inhbb	inhibin beta-B	gene	MP:0003346	abnormal pectoral muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10810	Inhbb	inhibin beta-B	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0004855	increased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0005131	increased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20241121	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7947320
10810	Inhbb	inhibin beta-B	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20241121	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20241121	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20241121	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20241121	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20241121	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0009363	abnormal tertiary ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20220407	MGI			PMID:17609433
10810	Inhbb	inhibin beta-B	gene	MP:0009505	abnormal mammary gland lobule morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885473
10810	Inhbb	inhibin beta-B	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
10810	Inhbb	inhibin beta-B	gene	MP:0010238	increased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20810712
10810	Inhbb	inhibin beta-B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8125256
10810	Inhbb	inhibin beta-B	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885473
10810	Inhbb	inhibin beta-B	gene	MP:0013718	galactostasis		IAGP		N	RGD:5509061	20150402	MGI			PMID:8125256
10811	Ins1	insulin I	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20180719	MGI			PMID:15889095
10811	Ins1	insulin I	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:15889095
10811	Ins1	insulin I	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11272179
10811	Ins1	insulin I	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26769314
10811	Ins1	insulin I	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0002869	increased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0002870	decreased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20180719	MGI			PMID:15889095
10811	Ins1	insulin I	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20210617	MGI			PMID:29864031
10811	Ins1	insulin I	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20210617	MGI			PMID:29864031
10811	Ins1	insulin I	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:11272179
10811	Ins1	insulin I	gene	MP:0003926	decreased cellular glucose uptake		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20180719	MGI			PMID:15889095
10811	Ins1	insulin I	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20180719	MGI			PMID:12925730
10811	Ins1	insulin I	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20180719	MGI			PMID:15889095
10811	Ins1	insulin I	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210617	MGI			PMID:29864031
10811	Ins1	insulin I	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20180719	MGI			PMID:15889095
10811	Ins1	insulin I	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20180719	MGI			PMID:11272179
10811	Ins1	insulin I	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20180719	MGI			PMID:11897712
10811	Ins1	insulin I	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20180719	MGI			PMID:11897712
10811	Ins1	insulin I	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:11897712
10811	Ins1	insulin I	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:11897712
10811	Ins1	insulin I	gene	MP:0010147	abnormal endocrine pancreas physiology		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:19680229
10811	Ins1	insulin I	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:9144203
10811	Ins1	insulin I	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11897712
10811	Ins1	insulin I	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20210617	MGI			PMID:29864031
10811	Ins1	insulin I	gene	MP:0014109	increased pancreatic alpha cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11897712
10811	Ins1	insulin I	gene	MP:0014122	decreased pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11897712
10811	Ins1	insulin I	gene	MP:0014122	decreased pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:25830089
10811	Ins1	insulin I	gene	MP:0020423	abnormal mitochondrial biogenesis		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
10811	Ins1	insulin I	gene	MP:0030589	increased pancreatic alpha cell mass		IAGP		N	RGD:5509061	20180719	MGI			PMID:11897712
10812	Ins2	insulin II	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731364
10812	Ins2	insulin II	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16964447
10812	Ins2	insulin II	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20170413	MGI			PMID:27820699
10812	Ins2	insulin II	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133560
10812	Ins2	insulin II	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16964447
10812	Ins2	insulin II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334640
10812	Ins2	insulin II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
10812	Ins2	insulin II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240801	MGI			PMID:35108512
10812	Ins2	insulin II	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334640
10812	Ins2	insulin II	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334640
10812	Ins2	insulin II	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133560
10812	Ins2	insulin II	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334640
10812	Ins2	insulin II	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11981430
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334640
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056790
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133560
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9593767
10812	Ins2	insulin II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20201224	MGI			PMID:32699230
10812	Ins2	insulin II	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133560
10812	Ins2	insulin II	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133560
10812	Ins2	insulin II	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20201224	MGI			PMID:32699230
10812	Ins2	insulin II	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20201224	MGI			PMID:32699230
10812	Ins2	insulin II	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889095
10812	Ins2	insulin II	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889095
10812	Ins2	insulin II	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11272179
10812	Ins2	insulin II	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925730
10812	Ins2	insulin II	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
10812	Ins2	insulin II	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16964447
10812	Ins2	insulin II	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9593767
10812	Ins2	insulin II	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11981430
10812	Ins2	insulin II	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133560
10812	Ins2	insulin II	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19684026
10812	Ins2	insulin II	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334640
10812	Ins2	insulin II	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10812	Ins2	insulin II	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10812	Ins2	insulin II	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133560
10812	Ins2	insulin II	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20240801	MGI			PMID:35108512
10812	Ins2	insulin II	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0002869	increased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925730
10812	Ins2	insulin II	gene	MP:0002869	increased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889095
10812	Ins2	insulin II	gene	MP:0002869	increased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0002870	decreased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889095
10812	Ins2	insulin II	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11981430
10812	Ins2	insulin II	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20150611	MGI			PMID:11272179
10812	Ins2	insulin II	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10812	Ins2	insulin II	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
10812	Ins2	insulin II	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
10812	Ins2	insulin II	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133560
10812	Ins2	insulin II	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9593767
10812	Ins2	insulin II	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20150611	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
10812	Ins2	insulin II	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20240801	MGI			PMID:35108512
10812	Ins2	insulin II	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11272179
10812	Ins2	insulin II	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925730
10812	Ins2	insulin II	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16804066
10812	Ins2	insulin II	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889095
10812	Ins2	insulin II	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20240801	MGI			PMID:35108512
10812	Ins2	insulin II	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
10812	Ins2	insulin II	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:32699230
10812	Ins2	insulin II	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:35108512
10812	Ins2	insulin II	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9593767
10812	Ins2	insulin II	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9593767
10812	Ins2	insulin II	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:32699230
10812	Ins2	insulin II	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
10812	Ins2	insulin II	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
10812	Ins2	insulin II	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133560
10812	Ins2	insulin II	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20201224	MGI			PMID:32699230
10812	Ins2	insulin II	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20240801	MGI			PMID:35108512
10812	Ins2	insulin II	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10812	Ins2	insulin II	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0005527	increased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889095
10812	Ins2	insulin II	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16804066
10812	Ins2	insulin II	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16964447
10812	Ins2	insulin II	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10812	Ins2	insulin II	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
10812	Ins2	insulin II	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
10812	Ins2	insulin II	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
10812	Ins2	insulin II	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
10812	Ins2	insulin II	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:11981430
10812	Ins2	insulin II	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258336
10812	Ins2	insulin II	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0009112	abnormal pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10812	Ins2	insulin II	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11272179
10812	Ins2	insulin II	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897712
10812	Ins2	insulin II	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10812	Ins2	insulin II	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
10812	Ins2	insulin II	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897712
10812	Ins2	insulin II	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
10812	Ins2	insulin II	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:9593767
10812	Ins2	insulin II	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20201224	MGI			PMID:32699230
10812	Ins2	insulin II	gene	MP:0009174	absent pancreatic beta cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303807
10812	Ins2	insulin II	gene	MP:0009255	degranulated pancreatic beta cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9593767
10812	Ins2	insulin II	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897712
10812	Ins2	insulin II	gene	MP:0009488	abnormal pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10812	Ins2	insulin II	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897712
10812	Ins2	insulin II	gene	MP:0010145	abnormal spermatic cord morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20240801	MGI			PMID:35108512
10812	Ins2	insulin II	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15587270
10812	Ins2	insulin II	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
10812	Ins2	insulin II	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19680229
10812	Ins2	insulin II	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144203
10812	Ins2	insulin II	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0011425	abnormal kidney interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0011430	mesangiolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0011638	abnormal mitochondrial chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16604193
10812	Ins2	insulin II	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20180614	MGI			PMID:11897712
10812	Ins2	insulin II	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
10812	Ins2	insulin II	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
10812	Ins2	insulin II	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334640
10812	Ins2	insulin II	gene	MP:0014109	increased pancreatic alpha cell proliferation		IAGP		N	RGD:5509061	20180614	MGI			PMID:11897712
10812	Ins2	insulin II	gene	MP:0014117	increased pancreatic beta cell apoptosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
10812	Ins2	insulin II	gene	MP:0014121	increased pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20160324	MGI			PMID:19955657
10812	Ins2	insulin II	gene	MP:0014122	decreased pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20180614	MGI			PMID:11897712
10812	Ins2	insulin II	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20170803	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:22297672
10812	Ins2	insulin II	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:15914643
10812	Ins2	insulin II	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0030589	increased pancreatic alpha cell mass		IAGP		N	RGD:5509061	20180614	MGI			PMID:11897712
10812	Ins2	insulin II	gene	MP:0031414	decreased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:17911348
10812	Ins2	insulin II	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:17911348
10813	Insr	insulin receptor	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288891
10813	Insr	insulin receptor	gene	MP:0000199	abnormal circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
10813	Insr	insulin receptor	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
10813	Insr	insulin receptor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20180628	MGI			PMID:26868295
10813	Insr	insulin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20191226	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8528241
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844629
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20180628	MGI			PMID:26868295
10813	Insr	insulin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
10813	Insr	insulin receptor	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288891
10813	Insr	insulin receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20180628	MGI			PMID:26868295
10813	Insr	insulin receptor	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20191226	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0001868	ovary inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12219087
10813	Insr	insulin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12488434
10813	Insr	insulin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581004
10813	Insr	insulin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288891
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22055502
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8528241
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844629
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20180628	MGI			PMID:26868295
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
10813	Insr	insulin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20220811	MGI			PMID:34460911
10813	Insr	insulin receptor	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12219087
10813	Insr	insulin receptor	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12488434
10813	Insr	insulin receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628051
10813	Insr	insulin receptor	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8528241
10813	Insr	insulin receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:34460911
10813	Insr	insulin receptor	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0002893	ketoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
10813	Insr	insulin receptor	gene	MP:0002893	ketoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0002893	ketoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:8528241
10813	Insr	insulin receptor	gene	MP:0002893	ketoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628051
10813	Insr	insulin receptor	gene	MP:0002996	ovotestis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628051
10813	Insr	insulin receptor	gene	MP:0003023	decreased coronary flow rate		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
10813	Insr	insulin receptor	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0003839	abnormal insulin clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0003916	decreased heart left ventricle weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0003959	abnormal lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0004039	abnormal cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372107
10813	Insr	insulin receptor	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844629
10813	Insr	insulin receptor	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288891
10813	Insr	insulin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
10813	Insr	insulin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
10813	Insr	insulin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20180628	MGI			PMID:26868295
10813	Insr	insulin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
10813	Insr	insulin receptor	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844629
10813	Insr	insulin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288891
10813	Insr	insulin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22055502
10813	Insr	insulin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20180628	MGI			PMID:26868295
10813	Insr	insulin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
10813	Insr	insulin receptor	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9844629
10813	Insr	insulin receptor	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372107
10813	Insr	insulin receptor	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12219087
10813	Insr	insulin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
10813	Insr	insulin receptor	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0006353	increased glycosylated hemoglobin level		IEA		N	RGD:5509061	20111116	MGI			
10813	Insr	insulin receptor	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20190103	MGI			
10813	Insr	insulin receptor	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372107
10813	Insr	insulin receptor	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288891
10813	Insr	insulin receptor	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20180628	MGI			PMID:26868295
10813	Insr	insulin receptor	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288891
10813	Insr	insulin receptor	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20180614	MGI			PMID:15372107
10813	Insr	insulin receptor	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0009174	absent pancreatic beta cells		IAGP		N	RGD:5509061	20180614	MGI			PMID:12488434
10813	Insr	insulin receptor	gene	MP:0009342	enlarged gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0009462	skeletal muscle hypotrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17416680
10813	Insr	insulin receptor	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
10813	Insr	insulin receptor	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:34460911
10813	Insr	insulin receptor	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20220811	MGI			PMID:34460911
10813	Insr	insulin receptor	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
10813	Insr	insulin receptor	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
10813	Insr	insulin receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12459269
10813	Insr	insulin receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254588
10813	Insr	insulin receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8528241
10813	Insr	insulin receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612577
10813	Insr	insulin receptor	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:11000114
10813	Insr	insulin receptor	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0011943	abnormal circadian feeding behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266328
10813	Insr	insulin receptor	gene	MP:0013925	abnormal vascular plexus formation		IAGP		N	RGD:5509061	20220811	MGI			PMID:34460911
10813	Insr	insulin receptor	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:17189427
10813	Insr	insulin receptor	gene	MP:0014605	dark liver		IAGP		N	RGD:5509061	20250206	MGI			PMID:10949030
10813	Insr	insulin receptor	gene	MP:0014998	abnormal glucose metabolism		IAGP		N	RGD:5509061	20260611	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0015000	decreased glucose oxidation		IAGP		N	RGD:5509061	20260611	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0015068	decreased myocardial fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0015070	decreased myocardial fiber length		IAGP		N	RGD:5509061	20260813	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170202	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0030018	increased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0030020	decreased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20200402	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0030971	ketoacidosis		IAGP		N	RGD:5509061	20190815	MGI			PMID:15713666
10813	Insr	insulin receptor	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:23119079
10813	Insr	insulin receptor	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:11877471
10813	Insr	insulin receptor	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:17189427
10815	Irf1	interferon regulatory factor 1	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7957048
10815	Irf1	interferon regulatory factor 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
10815	Irf1	interferon regulatory factor 1	gene	MP:0001573	abnormal circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410367
10815	Irf1	interferon regulatory factor 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9317154
10815	Irf1	interferon regulatory factor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346812
10815	Irf1	interferon regulatory factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
10815	Irf1	interferon regulatory factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
10815	Irf1	interferon regulatory factor 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9317154
10815	Irf1	interferon regulatory factor 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123129
10815	Irf1	interferon regulatory factor 1	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346812
10815	Irf1	interferon regulatory factor 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
10815	Irf1	interferon regulatory factor 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
10815	Irf1	interferon regulatory factor 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
10815	Irf1	interferon regulatory factor 1	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9317154
10815	Irf1	interferon regulatory factor 1	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346812
10815	Irf1	interferon regulatory factor 1	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240709
10815	Irf1	interferon regulatory factor 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240709
10815	Irf1	interferon regulatory factor 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
10815	Irf1	interferon regulatory factor 1	gene	MP:0004798	decreased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
10815	Irf1	interferon regulatory factor 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807824
10815	Irf1	interferon regulatory factor 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12499398
10815	Irf1	interferon regulatory factor 1	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20190110	MGI			
10815	Irf1	interferon regulatory factor 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
10815	Irf1	interferon regulatory factor 1	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IEA		N	RGD:5509061	20111116	MGI			
10815	Irf1	interferon regulatory factor 1	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
10815	Irf1	interferon regulatory factor 1	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807824
10815	Irf1	interferon regulatory factor 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
10815	Irf1	interferon regulatory factor 1	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
10815	Irf1	interferon regulatory factor 1	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7957048
10815	Irf1	interferon regulatory factor 1	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8885869
10815	Irf1	interferon regulatory factor 1	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20111116	MGI			
10815	Irf1	interferon regulatory factor 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
10815	Irf1	interferon regulatory factor 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
10815	Irf1	interferon regulatory factor 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7957048
10815	Irf1	interferon regulatory factor 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
10815	Irf1	interferon regulatory factor 1	gene	MP:0008090	increased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9379011
10815	Irf1	interferon regulatory factor 1	gene	MP:0008563	decreased interferon-alpha secretion		IEA		N	RGD:5509061	20111116	MGI			
10815	Irf1	interferon regulatory factor 1	gene	MP:0008565	decreased interferon-beta secretion		IEA		N	RGD:5509061	20111116	MGI			
10815	Irf1	interferon regulatory factor 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240709
10815	Irf1	interferon regulatory factor 1	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9379011
10815	Irf1	interferon regulatory factor 1	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807824
10815	Irf1	interferon regulatory factor 1	gene	MP:0008590	abnormal circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807824
10815	Irf1	interferon regulatory factor 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807824
10815	Irf1	interferon regulatory factor 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9379011
10815	Irf1	interferon regulatory factor 1	gene	MP:0008600	decreased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9379011
10815	Irf1	interferon regulatory factor 1	gene	MP:0008601	abnormal circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807824
10815	Irf1	interferon regulatory factor 1	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9379011
10815	Irf1	interferon regulatory factor 1	gene	MP:0008608	increased circulating interleukin-13 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807824
10815	Irf1	interferon regulatory factor 1	gene	MP:0008623	increased circulating interleukin-3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9379011
10815	Irf1	interferon regulatory factor 1	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807824
10815	Irf1	interferon regulatory factor 1	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9379011
10815	Irf1	interferon regulatory factor 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807824
10815	Irf1	interferon regulatory factor 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9379011
10815	Irf1	interferon regulatory factor 1	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:8885869
10815	Irf1	interferon regulatory factor 1	gene	MP:0009332	abnormal splenocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7957048
10815	Irf1	interferon regulatory factor 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240709
10815	Irf1	interferon regulatory factor 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346812
10815	Irf1	interferon regulatory factor 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240709
10815	Irf1	interferon regulatory factor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:10346812
10815	Irf1	interferon regulatory factor 1	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:9472983
10815	Irf1	interferon regulatory factor 1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
10815	Irf1	interferon regulatory factor 1	gene	MP:0020928	increased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16123129
10816	Irs1	insulin receptor substrate 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074531
10816	Irs1	insulin receptor substrate 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
10816	Irs1	insulin receptor substrate 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736890
10816	Irs1	insulin receptor substrate 1	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9541510
10816	Irs1	insulin receptor substrate 1	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:9541510
10816	Irs1	insulin receptor substrate 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736890
10816	Irs1	insulin receptor substrate 1	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0000589	thin tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:20837540
10816	Irs1	insulin receptor substrate 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074531
10816	Irs1	insulin receptor substrate 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467829
10816	Irs1	insulin receptor substrate 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074531
10816	Irs1	insulin receptor substrate 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20837540
10816	Irs1	insulin receptor substrate 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7526222
10816	Irs1	insulin receptor substrate 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7969452
10816	Irs1	insulin receptor substrate 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062343
10816	Irs1	insulin receptor substrate 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9541510
10816	Irs1	insulin receptor substrate 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20837540
10816	Irs1	insulin receptor substrate 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7526222
10816	Irs1	insulin receptor substrate 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892694
10816	Irs1	insulin receptor substrate 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9541510
10816	Irs1	insulin receptor substrate 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810606
10816	Irs1	insulin receptor substrate 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9541510
10816	Irs1	insulin receptor substrate 1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810606
10816	Irs1	insulin receptor substrate 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467829
10816	Irs1	insulin receptor substrate 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7969452
10816	Irs1	insulin receptor substrate 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062343
10816	Irs1	insulin receptor substrate 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
10816	Irs1	insulin receptor substrate 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259600
10816	Irs1	insulin receptor substrate 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7969452
10816	Irs1	insulin receptor substrate 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590692
10816	Irs1	insulin receptor substrate 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074531
10816	Irs1	insulin receptor substrate 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7526222
10816	Irs1	insulin receptor substrate 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7969452
10816	Irs1	insulin receptor substrate 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062343
10816	Irs1	insulin receptor substrate 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20837540
10816	Irs1	insulin receptor substrate 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20837540
10816	Irs1	insulin receptor substrate 1	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7969452
10816	Irs1	insulin receptor substrate 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20837540
10816	Irs1	insulin receptor substrate 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467829
10816	Irs1	insulin receptor substrate 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0002999	abnormal bone healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736890
10816	Irs1	insulin receptor substrate 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11078455
10816	Irs1	insulin receptor substrate 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736890
10816	Irs1	insulin receptor substrate 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7969452
10816	Irs1	insulin receptor substrate 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590692
10816	Irs1	insulin receptor substrate 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810606
10816	Irs1	insulin receptor substrate 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259600
10816	Irs1	insulin receptor substrate 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467829
10816	Irs1	insulin receptor substrate 1	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074531
10816	Irs1	insulin receptor substrate 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074531
10816	Irs1	insulin receptor substrate 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7526222
10816	Irs1	insulin receptor substrate 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062343
10816	Irs1	insulin receptor substrate 1	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810606
10816	Irs1	insulin receptor substrate 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590692
10816	Irs1	insulin receptor substrate 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074531
10816	Irs1	insulin receptor substrate 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7526222
10816	Irs1	insulin receptor substrate 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7969452
10816	Irs1	insulin receptor substrate 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062343
10816	Irs1	insulin receptor substrate 1	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062343
10816	Irs1	insulin receptor substrate 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810606
10816	Irs1	insulin receptor substrate 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9541510
10816	Irs1	insulin receptor substrate 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810606
10816	Irs1	insulin receptor substrate 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9541510
10816	Irs1	insulin receptor substrate 1	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9541510
10816	Irs1	insulin receptor substrate 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
10816	Irs1	insulin receptor substrate 1	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:9062343
10816	Irs1	insulin receptor substrate 1	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7969452
10816	Irs1	insulin receptor substrate 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7526222
10816	Irs1	insulin receptor substrate 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20837540
10816	Irs1	insulin receptor substrate 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736890
10816	Irs1	insulin receptor substrate 1	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:18590693
10816	Irs1	insulin receptor substrate 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10816	Irs1	insulin receptor substrate 1	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20032200
10816	Irs1	insulin receptor substrate 1	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:10749573
10816	Irs1	insulin receptor substrate 1	gene	MP:0030439	decreased osteoblast proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:20032200
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20105241
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904471
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904471
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20171228	MGI			PMID:28806779
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20105241
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0006323	abnormal extraembryonic mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20171228	MGI			PMID:28806779
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0010466	vascular ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570943
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20171228	MGI			PMID:28806779
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0012183	decreased paraxial mesoderm size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7508365
10817	Itga5	integrin alpha 5 (fibronectin receptor alpha)	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:20570943
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20201001	MGI			PMID:30856165
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0004092	absent Z line		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10820	Itpa	inosine triphosphatase (nucleoside triphosphate pyrophosphatase)	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19498443
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9302515
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8538767
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23884927
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23884927
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8530061
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987786
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9302515
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27108798
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8530061
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987786
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23884927
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8538767
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9302515
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20150730	MGI			
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20111116	MGI			
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001525	impaired balance		IEA		N	RGD:5509061	20111116	MGI			
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170105	MGI			
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:23884927
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8530061
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8538767
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987786
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9302515
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17590087
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:23884927
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0002880	opisthotonus		IEA		N	RGD:5509061	20111116	MGI			
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8538767
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23884927
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20150827	MGI			PMID:26168218
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9302515
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17590087
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8538767
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0004930	small epididymis		IEA		N	RGD:5509061	20170105	MGI			
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20150827	MGI			PMID:26168218
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9302515
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20260402	MGI			
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0006156	abnormal visual pursuit		IAGP		N	RGD:5509061	20141003	MGI			PMID:23884927
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23884927
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8530061
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8987786
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8538767
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8538767
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
10821	Itpr1	inositol 1,4,5-trisphosphate receptor 1	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:23884927
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3996911
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0000416	sparse hair		IEA		N	RGD:5509061	20141003	MGI			
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0000427	abnormal hair cycle		IEA		N	RGD:5509061	20141003	MGI			
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20160512	MGI			PMID:25879444
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20211021	MGI			
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23859941
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20160512	MGI			PMID:18728777
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20210520	MGI			
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20160512	MGI			PMID:17559418
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20160512	MGI			PMID:17559418
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:23859941
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20160512	MGI			PMID:17559418
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20160512	MGI			PMID:18728777
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0001985	abnormal gustatory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23859941
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:3996911
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:924142
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20160512	MGI			PMID:25879444
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20160512	MGI			PMID:25879444
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002791	steatorrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20160512	MGI			PMID:18728777
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0002969	impaired social transmission of food preference		IAGP		N	RGD:5509061	20160512	MGI			PMID:17559418
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20160512	MGI			PMID:17559418
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0003867	increased defecation amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0004179	transmission ratio distortion		IEA		N	RGD:5509061	20141003	MGI			
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0005310	abnormal salivary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0008222	decreased hippocampal commissure size		IAGP		N	RGD:5509061	20160512	MGI			PMID:25879444
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20160512	MGI			PMID:25879444
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20160512	MGI			PMID:25879444
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0009161	pancreatic acinar cell zymogen granule accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195467
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0011000	abnormal allogrooming behavior		IAGP		N	RGD:5509061	20160512	MGI			PMID:17559418
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23859941
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0012347	low sweet preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:23859941
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0013140	excessive vocalization		IAGP		N	RGD:5509061	20160512	MGI			PMID:18728777
10822	Itpr3	inositol 1,4,5-triphosphate receptor 3	gene	MP:0014476	abnormal feces lipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:16195467
10823	Jak2	Janus kinase 2	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
10823	Jak2	Janus kinase 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590173
10823	Jak2	Janus kinase 2	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590174
10823	Jak2	Janus kinase 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590173
10823	Jak2	Janus kinase 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590173
10823	Jak2	Janus kinase 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:24169825
10823	Jak2	Janus kinase 2	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169911
10823	Jak2	Janus kinase 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086539
10823	Jak2	Janus kinase 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590174
10823	Jak2	Janus kinase 2	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590174
10823	Jak2	Janus kinase 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887119
10823	Jak2	Janus kinase 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169911
10823	Jak2	Janus kinase 2	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086539
10823	Jak2	Janus kinase 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:24169825
10823	Jak2	Janus kinase 2	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
10823	Jak2	Janus kinase 2	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
10823	Jak2	Janus kinase 2	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
10823	Jak2	Janus kinase 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086539
10823	Jak2	Janus kinase 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
10823	Jak2	Janus kinase 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887119
10823	Jak2	Janus kinase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24169825
10823	Jak2	Janus kinase 2	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169911
10823	Jak2	Janus kinase 2	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169911
10823	Jak2	Janus kinase 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086539
10823	Jak2	Janus kinase 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20150702	MGI			PMID:25552701
10823	Jak2	Janus kinase 2	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
10823	Jak2	Janus kinase 2	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0008976	delayed female fertility		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0009015	short proestrus		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0009020	prolonged metestrus		IAGP		N	RGD:5509061	20220203	MGI			PMID:21209203
10823	Jak2	Janus kinase 2	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169911
10823	Jak2	Janus kinase 2	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169911
10823	Jak2	Janus kinase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590173
10823	Jak2	Janus kinase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887119
10823	Jak2	Janus kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24169825
10823	Jak2	Janus kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590174
10823	Jak2	Janus kinase 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086539
10823	Jak2	Janus kinase 2	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0011746	spleen fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0011746	spleen fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144185
10823	Jak2	Janus kinase 2	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23863895
10823	Jak2	Janus kinase 2	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20211104	MGI			PMID:20489053
10823	Jak2	Janus kinase 2	gene	MP:0013147	limb paralysis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:15169911
10823	Jak2	Janus kinase 2	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:16887119
10823	Jak2	Janus kinase 2	gene	MP:0020399	enhanced megakaryocyte emperipolesis		IAGP		N	RGD:5509061	20170803	MGI			PMID:20541703
10823	Jak2	Janus kinase 2	gene	MP:0020463	increased megakaryocyte progenitor cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
10823	Jak2	Janus kinase 2	gene	MP:0030025	giant platelets		IAGP		N	RGD:5509061	20170803	MGI			PMID:20472827
10823	Jak2	Janus kinase 2	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:24169825
10824	Jak3	Janus kinase 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20111116	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0000493	rectal prolapse		IEA		N	RGD:5509061	20111116	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878135
10824	Jak3	Janus kinase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887051
10824	Jak3	Janus kinase 3	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878135
10824	Jak3	Janus kinase 3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11034372
10824	Jak3	Janus kinase 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20231207	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0001606	impaired hematopoiesis		IEA		N	RGD:5509061	20151119	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230601	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887051
10824	Jak3	Janus kinase 3	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0001806	decreased IgM level		IEA		N	RGD:5509061	20190606	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887051
10824	Jak3	Janus kinase 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9016869
10824	Jak3	Janus kinase 3	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9016869
10824	Jak3	Janus kinase 3	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20111116	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993294
10824	Jak3	Janus kinase 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11034372
10824	Jak3	Janus kinase 3	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210520	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887051
10824	Jak3	Janus kinase 3	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878135
10824	Jak3	Janus kinase 3	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16020505
10824	Jak3	Janus kinase 3	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878135
10824	Jak3	Janus kinase 3	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15147562
10824	Jak3	Janus kinase 3	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9016869
10824	Jak3	Janus kinase 3	gene	MP:0002497	increased IgE level		IEA		N	RGD:5509061	20150305	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878135
10824	Jak3	Janus kinase 3	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878135
10824	Jak3	Janus kinase 3	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0003304	large intestinal inflammation		IEA		N	RGD:5509061	20111116	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0003944	abnormal T cell subpopulation ratio		IEA		N	RGD:5509061	20111116	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15147562
10824	Jak3	Janus kinase 3	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0004978	decreased B-1 B cell number		IEA		N	RGD:5509061	20151119	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20150305	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993294
10824	Jak3	Janus kinase 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20111116	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0005036	diarrhea		IEA		N	RGD:5509061	20111116	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887051
10824	Jak3	Janus kinase 3	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9016869
10824	Jak3	Janus kinase 3	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0005425	increased macrophage cell number		IEA		N	RGD:5509061	20151119	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16020505
10824	Jak3	Janus kinase 3	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9016869
10824	Jak3	Janus kinase 3	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20190411	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0008046	absent NK cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9016869
10824	Jak3	Janus kinase 3	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887051
10824	Jak3	Janus kinase 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16020505
10824	Jak3	Janus kinase 3	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IEA		N	RGD:5509061	20190411	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16020505
10824	Jak3	Janus kinase 3	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887051
10824	Jak3	Janus kinase 3	gene	MP:0008082	increased single-positive T cell number		IEA		N	RGD:5509061	20150305	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20150305	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16020505
10824	Jak3	Janus kinase 3	gene	MP:0008121	increased myeloid dendritic cell number		IEA		N	RGD:5509061	20151119	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008122	decreased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16020505
10824	Jak3	Janus kinase 3	gene	MP:0008127	decreased dendritic cell number		IEA		N	RGD:5509061	20190606	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20190606	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20190606	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0008728	increased memory B cell number		IEA		N	RGD:5509061	20150305	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008729	decreased memory B cell number		IEA		N	RGD:5509061	20151119	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16020505
10824	Jak3	Janus kinase 3	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:7481767
10824	Jak3	Janus kinase 3	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9016869
10824	Jak3	Janus kinase 3	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0009540	absent Hassall's corpuscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363534
10824	Jak3	Janus kinase 3	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20150305	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20150305	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0012671	retina spots		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
10824	Jak3	Janus kinase 3	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:8777722
10824	Jak3	Janus kinase 3	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:10419884
10824	Jak3	Janus kinase 3	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20150305	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20150305	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
10824	Jak3	Janus kinase 3	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
10825	Espn	espin	gene	MP:0000026	abnormal inner ear morphology		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0000034	abnormal inner ear vestibule morphology		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1636414
10825	Espn	espin	gene	MP:0000048	abnormal stria vascularis morphology		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16588504
10825	Espn	espin	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16588504
10825	Espn	espin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
10825	Espn	espin	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16588504
10825	Espn	espin	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
10825	Espn	espin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16588504
10825	Espn	espin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1636414
10825	Espn	espin	gene	MP:0002630	abnormal endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20141003	MGI			PMID:16588504
10825	Espn	espin	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0002855	abnormal cochlear ganglion morphology		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0002857	cochlear ganglion degeneration		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0002895	abnormal otolithic membrane morphology		IEA		N	RGD:5509061	20111229	MGI			
10825	Espn	espin	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0003150	detached tectorial membrane		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
10825	Espn	espin	gene	MP:0003878	abnormal ear physiology		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0004324	vestibular hair cell degeneration		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0004331	vestibular saccular macula degeneration		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0004333	abnormal utricular macula morphology		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1636414
10825	Espn	espin	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1636414
10825	Espn	espin	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1636414
10825	Espn	espin	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0004409	abnormal crista ampullaris neuroepithelium morphology		IEA		N	RGD:5509061	20111116	MGI			
10825	Espn	espin	gene	MP:0004413	absent cochlear microphonics		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0004416	absent cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:26926603
10825	Espn	espin	gene	MP:0004519	thin vestibular hair cell stereocilia		IAGP		N	RGD:5509061	20240321	MGI			PMID:26926603
10825	Espn	espin	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1636414
10825	Espn	espin	gene	MP:0004523	decreased cochlear hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16206170
10825	Espn	espin	gene	MP:0004524	short cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16206170
10825	Espn	espin	gene	MP:0004525	thin cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16206170
10825	Espn	espin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:26926603
10825	Espn	espin	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1636414
10825	Espn	espin	gene	MP:0004586	pillar cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1636414
10825	Espn	espin	gene	MP:0004586	pillar cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
10825	Espn	espin	gene	MP:0004813	absent linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
10825	Espn	espin	gene	MP:0004814	reduced linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
10825	Espn	espin	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
10825	Espn	espin	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
10825	Espn	espin	gene	MP:0006335	abnormal hearing electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6871029
10825	Espn	espin	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20141003	MGI			
10825	Espn	espin	gene	MP:0008763	abnormal mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962054
10825	Espn	espin	gene	MP:0010323	retropulsion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16588504
10825	Espn	espin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
10825	Espn	espin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:1636414
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441295
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441295
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080190
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20201022	MGI			
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000608	dissociated hepatocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21827743
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21827743
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441295
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080190
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080190
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927562
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441295
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20201022	MGI			
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441295
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265050
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265050
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20201022	MGI			
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080190
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10352021
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002658	abnormal liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927562
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002748	abnormal pulmonary valve morphology		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080190
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20935640
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12163468
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893599
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927562
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10352021
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10352021
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:10352021
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441295
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441295
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20935640
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080190
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080190
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265050
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265050
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21827743
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0009859	eye opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791271
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10352021
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010605	thick pulmonary valve cusps		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010617	thick mitral valve cusps		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265050
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265050
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0010971	abnormal periosteum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163348
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441295
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8330736
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818961
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441295
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8371760
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300111
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8330736
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10352021
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0021160	decreased heart right ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:10352021
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0030002	increased lung apoptosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:22265050
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0031524	mitral valve hyperplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0031526	thin right ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0031529	pulmonary valve hyperplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:23437302
10828	Jun	Jun proto-oncogene, AP-1 transcription factor subunit	gene	MP:0031581	semilunar valve hyperplasia		IAGP		N	RGD:5509061	20240125	MGI			PMID:23437302
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634333
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925011
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925011
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634333
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925011
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634333
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634333
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634333
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634333
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634333
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925011
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634333
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20240523	MGI			
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0010540	long stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696761
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634333
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925011
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
10830	Kcna2	potassium voltage-gated channel, shaker-related subfamily, member 2	gene	MP:0014625	abnormal ictal brain wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:17925011
10831	Kcna4	potassium voltage-gated channel, shaker-related subfamily, member 4	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9547391
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055293
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055293
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20210520	MGI			
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055293
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481235
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0003488	decreased channel response intensity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055293
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055293
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481235
10832	Kcna5	potassium voltage-gated channel, shaker-related subfamily, member 5	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11349004
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0002916	increased synaptic depression		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0003469	decreased single cell response intensity		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517255
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260618	MGI			PMID:38266642
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0030143	facial muscle spasm		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0031334	increased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
10833	Kcnc1	potassium voltage gated channel, Shaw-related subfamily, member 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:11517255
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11223304
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000044	absent organ of Corti		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20201022	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20201231	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001396	unidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001454	abnormal cued conditioning behavior		IEA		N	RGD:5509061	20211021	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002894	abnormal otolith morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0003169	abnormal scala media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0003349	abnormal circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0003878	abnormal ear physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004114	abnormal atrioventricular node morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004117	abnormal atrioventricular bundle morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004119	hypokalemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9933245
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11223304
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004331	vestibular saccular macula degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004334	utricular macular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004397	absent cochlear inner hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004403	absent cochlear outer hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004405	absent cochlear hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004409	abnormal crista ampullaris neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11223304
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004530	absent outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20111116	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004775	abnormal vestibular dark cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11223304
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004775	abnormal vestibular dark cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004776	vestibular dark cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004813	absent linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004845	absent vestibuloocular reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0005633	increased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0006024	collapsed Reissner membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0006024	collapsed Reissner membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15243133
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8982171
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0008308	small scala media		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438691
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200514	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003695
10834	Kcne1	potassium voltage-gated channel, Isk-related subfamily, member 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20181122	MGI			PMID:23974906
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18026101
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984590
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984590
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20181122	MGI			PMID:23974906
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:18026101
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18026101
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20260618	MGI			PMID:11984590
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0010575	aortic arch dilation		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16688530
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18026101
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:16688530
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:18026101
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0031192	coronary artery spasm		IAGP		N	RGD:5509061	20201119	MGI			PMID:11984590
10835	Kcnj8	potassium inwardly-rectifying channel, subfamily J, member 8	gene	MP:0031732	ST segment elevation		IAGP		N	RGD:5509061	20260618	MGI			PMID:11984590
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065093
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606590
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000263	absent organized vascular network		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601855
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000263	absent organized vascular network		IAGP		N	RGD:5509061	20141003	MGI			PMID:15644447
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000263	absent organized vascular network		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606590
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15944181
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023706
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20160211	MGI			PMID:25417109
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668192
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15644447
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010698
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023706
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19644017
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668192
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606590
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:15644447
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:15644447
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668192
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601855
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010698
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15644447
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25417109
10836	Kdr	kinase insert domain protein receptor	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0003543	abnormal vascular endothelial cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601855
10836	Kdr	kinase insert domain protein receptor	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601855
10836	Kdr	kinase insert domain protein receptor	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010698
10836	Kdr	kinase insert domain protein receptor	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
10836	Kdr	kinase insert domain protein receptor	gene	MP:0004106	lymphatic vessel hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668192
10836	Kdr	kinase insert domain protein receptor	gene	MP:0004106	lymphatic vessel hyperplasia		IAGP		N	RGD:5509061	20160211	MGI			PMID:25417109
10836	Kdr	kinase insert domain protein receptor	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
10836	Kdr	kinase insert domain protein receptor	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010698
10836	Kdr	kinase insert domain protein receptor	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668192
10836	Kdr	kinase insert domain protein receptor	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15644447
10836	Kdr	kinase insert domain protein receptor	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606590
10836	Kdr	kinase insert domain protein receptor	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668192
10836	Kdr	kinase insert domain protein receptor	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
10836	Kdr	kinase insert domain protein receptor	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22753193
10836	Kdr	kinase insert domain protein receptor	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010698
10836	Kdr	kinase insert domain protein receptor	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
10836	Kdr	kinase insert domain protein receptor	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10836	Kdr	kinase insert domain protein receptor	gene	MP:0006323	abnormal extraembryonic mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15644447
10836	Kdr	kinase insert domain protein receptor	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20160211	MGI			PMID:25417109
10836	Kdr	kinase insert domain protein receptor	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668192
10836	Kdr	kinase insert domain protein receptor	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987638
10836	Kdr	kinase insert domain protein receptor	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505259
10836	Kdr	kinase insert domain protein receptor	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
10836	Kdr	kinase insert domain protein receptor	gene	MP:0010196	abnormal lymphatic vessel smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439428
10836	Kdr	kinase insert domain protein receptor	gene	MP:0010200	enlarged lymphatic vessel		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439428
10836	Kdr	kinase insert domain protein receptor	gene	MP:0010200	enlarged lymphatic vessel		IAGP		N	RGD:5509061	20160211	MGI			PMID:25417109
10836	Kdr	kinase insert domain protein receptor	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0010643	absent fourth pharyngeal arch		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0010939	abnormal mandibular prominence morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065093
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15644447
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887829
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606590
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601855
10836	Kdr	kinase insert domain protein receptor	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20160211	MGI			PMID:25417109
10836	Kdr	kinase insert domain protein receptor	gene	MP:0012756	impaired cranial neural crest cell differentiation		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20170928	MGI			PMID:21305688
10836	Kdr	kinase insert domain protein receptor	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596435
10837	Khk	ketohexokinase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0002310	decreased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10837	Khk	ketohexokinase	gene	MP:0031265	increased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20251127	MGI			PMID:22371574
10838	Zfp354a	zinc finger protein 354A	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
10838	Zfp354a	zinc finger protein 354A	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
10838	Zfp354a	zinc finger protein 354A	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
10838	Zfp354a	zinc finger protein 354A	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
10838	Zfp354a	zinc finger protein 354A	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230119	MGI			
10838	Zfp354a	zinc finger protein 354A	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230119	MGI			
10838	Zfp354a	zinc finger protein 354A	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20231207	MGI			
10843	Klkb1	kallikrein B, plasma 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201022	MGI			
10843	Klkb1	kallikrein B, plasma 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201231	MGI			
10843	Klkb1	kallikrein B, plasma 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20250508	MGI			
10843	Klkb1	kallikrein B, plasma 1	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258336
10843	Klkb1	kallikrein B, plasma 1	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258336
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164829
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000583	long toenails		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164829
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164829
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000866	cerebellum vermis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550718
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164829
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001349	excessive tearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20160512	MGI			PMID:26079769
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614101
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614101
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20127821
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614101
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20160512	MGI			PMID:26079769
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614101
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164829
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15067019
10850	L1cam	L1 cell adhesion molecule	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614101
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614101
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002733	abnormal thermal nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0005316	abnormal response to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20211118	MGI			PMID:18171935
10850	L1cam	L1 cell adhesion molecule	gene	MP:0005423	abnormal somatic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550718
10850	L1cam	L1 cell adhesion molecule	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164829
10850	L1cam	L1 cell adhesion molecule	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164829
10850	L1cam	L1 cell adhesion molecule	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550718
10850	L1cam	L1 cell adhesion molecule	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171935
10850	L1cam	L1 cell adhesion molecule	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20127821
10850	L1cam	L1 cell adhesion molecule	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0008534	enlarged fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580664
10850	L1cam	L1 cell adhesion molecule	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15067019
10850	L1cam	L1 cell adhesion molecule	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564762
10850	L1cam	L1 cell adhesion molecule	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15067019
10850	L1cam	L1 cell adhesion molecule	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427628
10850	L1cam	L1 cell adhesion molecule	gene	MP:0011275	abnormal behavioral response to light		IAGP		N	RGD:5509061	20160512	MGI			PMID:26079769
10850	L1cam	L1 cell adhesion molecule	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11164829
10850	L1cam	L1 cell adhesion molecule	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0012484	decreased corticospinal tract size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354804
10850	L1cam	L1 cell adhesion molecule	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20161013	MGI			PMID:11164829
10850	L1cam	L1 cell adhesion molecule	gene	MP:0014750	abnormal retinal ganglion cell axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:18171935
10853	Lalba	lactalbumin, alpha	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8022817
10853	Lalba	lactalbumin, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7708733
10853	Lalba	lactalbumin, alpha	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:7708733
10853	Lalba	lactalbumin, alpha	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:8022817
10854	Lamb2	laminin, beta 2	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531444
10854	Lamb2	laminin, beta 2	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531444
10854	Lamb2	laminin, beta 2	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885444
10854	Lamb2	laminin, beta 2	gene	MP:0001054	failure of neuromuscular synapse presynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885444
10854	Lamb2	laminin, beta 2	gene	MP:0001055	failure of neuromuscular synapse postsynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885444
10854	Lamb2	laminin, beta 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531444
10854	Lamb2	laminin, beta 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
10854	Lamb2	laminin, beta 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670489
10854	Lamb2	laminin, beta 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885444
10854	Lamb2	laminin, beta 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
10854	Lamb2	laminin, beta 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
10854	Lamb2	laminin, beta 2	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885444
10854	Lamb2	laminin, beta 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670489
10854	Lamb2	laminin, beta 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
10854	Lamb2	laminin, beta 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670489
10854	Lamb2	laminin, beta 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885444
10854	Lamb2	laminin, beta 2	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
10854	Lamb2	laminin, beta 2	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531444
10854	Lamb2	laminin, beta 2	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418794
10854	Lamb2	laminin, beta 2	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885444
10854	Lamb2	laminin, beta 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531444
10854	Lamb2	laminin, beta 2	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
10854	Lamb2	laminin, beta 2	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
10854	Lamb2	laminin, beta 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
10854	Lamb2	laminin, beta 2	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
10854	Lamb2	laminin, beta 2	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531444
10854	Lamb2	laminin, beta 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
10854	Lamb2	laminin, beta 2	gene	MP:0005567	decreased circulating total protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
10854	Lamb2	laminin, beta 2	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885444
10854	Lamb2	laminin, beta 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
10854	Lamb2	laminin, beta 2	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531444
10854	Lamb2	laminin, beta 2	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531444
10854	Lamb2	laminin, beta 2	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
10854	Lamb2	laminin, beta 2	gene	MP:0010235	abnormal retina inner limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
10854	Lamb2	laminin, beta 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7885444
10854	Lamb2	laminin, beta 2	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670489
10854	Lamb2	laminin, beta 2	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
10854	Lamb2	laminin, beta 2	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:24293254
10854	Lamb2	laminin, beta 2	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670489
10854	Lamb2	laminin, beta 2	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
10854	Lamb2	laminin, beta 2	gene	MP:0011856	abnormal glomerular filtration barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670489
10854	Lamb2	laminin, beta 2	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531444
10854	Lamb2	laminin, beta 2	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:10531444
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20241121	MGI			
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212251
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20241121	MGI			
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210826	MGI			
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10855	Lamp1	lysosomal-associated membrane protein 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10972293
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10972293
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:28526246
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10972293
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10972293
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10972293
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0003325	decreased liver function		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0003927	increased cellular glucose import		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0004114	abnormal atrioventricular node morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0004117	abnormal atrioventricular bundle morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:28526246
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20181220	MGI			PMID:28526246
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10972293
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10972293
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10972293
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:28526246
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0006142	abnormal sinoatrial node conduction		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:10972293
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0009122	decreased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121881
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20181220	MGI			PMID:28526246
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:28526246
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0020103	decreased hepatic glucose production		IAGP		N	RGD:5509061	20151112	MGI			PMID:25043815
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:28526246
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20231109	MGI			PMID:28526246
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0031078	increased circulating troponin T level		IAGP		N	RGD:5509061	20221006	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0031709	ventricular arrhythmia		IAGP		N	RGD:5509061	20260514	MGI			PMID:34459252
10857	Lamp2	lysosomal-associated membrane protein 2	gene	MP:0031757	second degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:34459252
10858	Anpep	alanyl aminopeptidase, membrane	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210520	MGI			
10858	Anpep	alanyl aminopeptidase, membrane	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20430777
10858	Anpep	alanyl aminopeptidase, membrane	gene	MP:0003711	pathological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360568
10858	Anpep	alanyl aminopeptidase, membrane	gene	MP:0005544	cornea deposits		IEA		N	RGD:5509061	20210520	MGI			
10858	Anpep	alanyl aminopeptidase, membrane	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20210520	MGI			
10858	Anpep	alanyl aminopeptidase, membrane	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20430777
10858	Anpep	alanyl aminopeptidase, membrane	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360568
10858	Anpep	alanyl aminopeptidase, membrane	gene	MP:0012075	impaired mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22983824
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9054454
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9188474
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9188474
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9054454
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9188474
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9054454
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9188474
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9188474
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9188474
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9054454
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9188474
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9054454
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9188474
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0006084	abnormal circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0011312	abnormal kidney afferent arteriole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278414
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466392
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0011579	decreased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10859	Lcat	lecithin cholesterol acyltransferase	gene	MP:0031084	decreased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:11278414
10863	Ldhb	lactate dehydrogenase B	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:32415082
10863	Ldhb	lactate dehydrogenase B	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20250925	MGI			PMID:32415082
10863	Ldhb	lactate dehydrogenase B	gene	MP:0004488	type II spiral ligament fibrocyte degeneration		IAGP		N	RGD:5509061	20250925	MGI			PMID:32415082
10863	Ldhb	lactate dehydrogenase B	gene	MP:0004490	type IV spiral ligament fibrocyte degeneration		IAGP		N	RGD:5509061	20250925	MGI			PMID:32415082
10863	Ldhb	lactate dehydrogenase B	gene	MP:0004523	decreased cochlear hair cell stereocilia number		IAGP		N	RGD:5509061	20250925	MGI			PMID:32415082
10863	Ldhb	lactate dehydrogenase B	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20250925	MGI			PMID:32415082
10863	Ldhb	lactate dehydrogenase B	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20250925	MGI			PMID:32415082
10863	Ldhb	lactate dehydrogenase B	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20181227	MGI			
10863	Ldhb	lactate dehydrogenase B	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20250925	MGI			PMID:32415082
10863	Ldhb	lactate dehydrogenase B	gene	MP:0014345	abnormal neuron mitochondrial morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:32415082
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16835442
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445560
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127462
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9598833
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000181	abnormal circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12746448
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138930
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445560
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12746448
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15472122
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15840700
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236385
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434491
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080197
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478727
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18666258
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820241
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8994037
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9701246
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12639996
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15596719
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873689
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820241
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20150101	MGI			PMID:25176150
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076954
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873689
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478727
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8994037
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15031124
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236385
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16150825
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530237
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720268
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530237
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530237
10864	Ldlr	low density lipoprotein receptor	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211093
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250194
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10777503
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001345	Meibomian gland atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10777503
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236385
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236385
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236385
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207278
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236385
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16835442
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18466986
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7538675
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445560
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445560
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983917
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12969990
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15840700
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820241
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7538675
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8941642
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8994037
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9598833
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9701246
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9734366
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445560
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15840700
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820241
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127462
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566402
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0001863	blood vessel inflammation		IAGP		N	RGD:5509061	20221215	MGI			PMID:33356393
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847522
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847522
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872464
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790756
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10777503
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076954
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7961705
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471052
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:33356393
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002323	decreased susceptibility to hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076954
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127462
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434491
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18006500
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19318355
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22484817
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9598833
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20150101	MGI			PMID:25176150
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002830	gallstones		IEA		N	RGD:5509061	20111116	MGI			
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790756
10864	Ldlr	low density lipoprotein receptor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15031124
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003075	abnormal response to CNS ischemic injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147818
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003099	retina detachment		IEA		N	RGD:5509061	20111116	MGI			
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15031124
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12639996
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003211	abnormal aorta elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21252156
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:12969990
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236385
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188600
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147818
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003692	xanthoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003692	xanthoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:10777503
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003692	xanthoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073773
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15596719
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17615372
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12639996
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17885219
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451340
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003897	abnormal ST segment duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15031124
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003947	abnormal cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076954
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12969990
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847522
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8941642
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20150101	MGI			PMID:25176150
10864	Ldlr	low density lipoprotein receptor	gene	MP:0003991	arteriosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17885219
10864	Ldlr	low density lipoprotein receptor	gene	MP:0004112	abnormal arteriole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16835442
10864	Ldlr	low density lipoprotein receptor	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230601	MGI			
10864	Ldlr	low density lipoprotein receptor	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20150101	MGI			PMID:25176150
10864	Ldlr	low density lipoprotein receptor	gene	MP:0004778	increased macrophage derived foam cell number		IEA		N	RGD:5509061	20111116	MGI			
10864	Ldlr	low density lipoprotein receptor	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12615659
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15031124
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005144	abnormal circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873689
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478727
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820241
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8941642
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8994037
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9734366
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873689
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10488949
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712412
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10777503
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445560
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983917
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12746448
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12969990
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15566430
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15840700
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236385
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17885219
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18466986
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7538675
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8941642
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9598833
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9701246
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20151001	MGI			PMID:8656070
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24935961
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076954
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12639996
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12746502
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15596719
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211093
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873689
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19318355
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22484817
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20220630	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20260430	MGI			PMID:29068315
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172117
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385042
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172117
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18006500
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20260430	MGI			PMID:29068315
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873689
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847522
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872464
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073773
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847522
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712412
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727439
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:10764675
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445560
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12615659
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12746502
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15031124
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834123
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211093
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434491
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565511
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880330
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038633
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17615372
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872464
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250194
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451340
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149301
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:8994037
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:9701246
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20151001	MGI			PMID:8656070
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20160218	MGI			PMID:24935961
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20170209	MGI			PMID:18160459
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127462
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038633
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478727
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18466986
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188600
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723498
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606463
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22484817
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20151001	MGI			PMID:8656070
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20160218	MGI			PMID:24935961
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005340	abnormal susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520791
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11581143
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983917
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12639996
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15596719
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565511
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624897
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873689
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478727
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18006500
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18192239
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9734366
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20150101	MGI			PMID:25176150
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20191219	MGI			PMID:30944250
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20201217	MGI			PMID:31163988
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11893779
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873689
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385042
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12746502
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847522
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872464
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873689
10864	Ldlr	low density lipoprotein receptor	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20201015	MGI			PMID:28636934
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880330
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147818
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147818
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006116	calcified aortic valve		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006134	artery occlusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006238	abnormal choriocapillaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172117
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006278	aortic aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
10864	Ldlr	low density lipoprotein receptor	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008243	abnormal macrophage derived foam cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17885219
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008294	abnormal adrenal gland zona fasciculata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008431	abnormal short-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207278
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008431	abnormal short-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:16835442
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236385
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250194
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18192239
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207278
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720268
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172117
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478727
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478727
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12746502
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20181227	MGI			
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22484817
10864	Ldlr	low density lipoprotein receptor	gene	MP:0008900	abnormal uterine fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445560
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326295
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12746502
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250194
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21252156
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847522
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20201015	MGI			PMID:28636934
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445560
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22484817
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20150101	MGI			PMID:25176150
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18160655
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010052	increased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18466986
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12937162
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010139	aortitis		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010161	decreased brain cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18466986
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010332	abnormal circulating apolipoprotein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010333	abnormal circulating apolipoprotein E level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010659	abdominal aorta aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
10864	Ldlr	low density lipoprotein receptor	gene	MP:0010997	decreased aorta wall thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21252156
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011081	decreased macrophage apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834123
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17155952
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17615372
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011572	abnormal aorta bulb morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011579	decreased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668345
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011897	decreased circulating unsaturated transferrin level		IEA		N	RGD:5509061	20181227	MGI			
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17960025
10864	Ldlr	low density lipoprotein receptor	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0012223	increased circulating prothrombin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434491
10864	Ldlr	low density lipoprotein receptor	gene	MP:0012224	abnormal sterol level		IAGP		N	RGD:5509061	20150101	MGI			PMID:25176150
10864	Ldlr	low density lipoprotein receptor	gene	MP:0012326	increased circulating antithrombin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434491
10864	Ldlr	low density lipoprotein receptor	gene	MP:0012329	increased circulating factor VIII level		IAGP		N	RGD:5509061	20201002	MGI			PMID:14739216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0012329	increased circulating factor VIII level		IAGP		N	RGD:5509061	20201002	MGI			PMID:15840700
10864	Ldlr	low density lipoprotein receptor	gene	MP:0012355	decreased prothrombin time		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434491
10864	Ldlr	low density lipoprotein receptor	gene	MP:0012358	decreased partial thromboplastin time		IAGP		N	RGD:5509061	20201002	MGI			PMID:16434491
10864	Ldlr	low density lipoprotein receptor	gene	MP:0012688	abnormal heart ventricles weight		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0013277	abnormal fasting circulating glucose level		IAGP		N	RGD:5509061	20160609	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0014329	abnormal Purkinje cell axon morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:11530237
10864	Ldlr	low density lipoprotein receptor	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:18410513
10864	Ldlr	low density lipoprotein receptor	gene	MP:0014476	abnormal feces lipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:25176150
10864	Ldlr	low density lipoprotein receptor	gene	MP:0020099	increased susceptibility to diet-induced aortic fatty streak lesions		IAGP		N	RGD:5509061	20200820	MGI			PMID:28917158
10864	Ldlr	low density lipoprotein receptor	gene	MP:0020325	abnormal beige fat cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:28636934
10864	Ldlr	low density lipoprotein receptor	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:11520791
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031076	decreased circulating troponin level		IAGP		N	RGD:5509061	20200618	MGI			PMID:15031124
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21690266
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031165	increased circulating von Willebrand factor level		IAGP		N	RGD:5509061	20201015	MGI			PMID:14739216
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031165	increased circulating von Willebrand factor level		IAGP		N	RGD:5509061	20201015	MGI			PMID:15840700
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031273	decreased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20210617	MGI			PMID:21252156
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031274	increased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:18466986
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031510	increased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:12690199
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031566	small aortic valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:25231636
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031632	increased lung cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18160655
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031683	abnormal cholesterol transport		IAGP		N	RGD:5509061	20251023	MGI			PMID:22484817
10864	Ldlr	low density lipoprotein receptor	gene	MP:0031683	abnormal cholesterol transport		IAGP		N	RGD:5509061	20251023	MGI			PMID:25176150
10865	Lepr	leptin receptor	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22414803
10865	Lepr	leptin receptor	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8177042
10865	Lepr	leptin receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8177042
10865	Lepr	leptin receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21745644
10865	Lepr	leptin receptor	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9299565
10865	Lepr	leptin receptor	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
10865	Lepr	leptin receptor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22281595
10865	Lepr	leptin receptor	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:431046
10865	Lepr	leptin receptor	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32233916
10865	Lepr	leptin receptor	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:431046
10865	Lepr	leptin receptor	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22281595
10865	Lepr	leptin receptor	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16113078
10865	Lepr	leptin receptor	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023554
10865	Lepr	leptin receptor	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10708583
10865	Lepr	leptin receptor	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22414803
10865	Lepr	leptin receptor	gene	MP:0000642	enlarged adrenal glands		IEA		N	RGD:5509061	20111116	MGI			
10865	Lepr	leptin receptor	gene	MP:0000643	absent adrenal medulla		IEA		N	RGD:5509061	20111116	MGI			
10865	Lepr	leptin receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22281595
10865	Lepr	leptin receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22281595
10865	Lepr	leptin receptor	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20170105	MGI			
10865	Lepr	leptin receptor	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6991317
10865	Lepr	leptin receptor	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502493
10865	Lepr	leptin receptor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0001143	constricted vagina orifice		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070774
10865	Lepr	leptin receptor	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602618
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502493
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15885672
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16919419
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20852026
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084451
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21745644
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:5918576
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9845674
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20151126	MGI			PMID:25353183
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20151203	MGI			PMID:24024119
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20190905	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:10708583
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602618
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730408
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12885755
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070774
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207242
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685168
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:16113078
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084451
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:21346177
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:6991317
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:8177042
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:9845674
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20150416	MGI			PMID:25157166
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20241212	MGI			PMID:36243005
10865	Lepr	leptin receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20241226	MGI			PMID:38987239
10865	Lepr	leptin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17415414
10865	Lepr	leptin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
10865	Lepr	leptin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
10865	Lepr	leptin receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15309293
10865	Lepr	leptin receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
10865	Lepr	leptin receptor	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16998795
10865	Lepr	leptin receptor	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043866
10865	Lepr	leptin receptor	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
10865	Lepr	leptin receptor	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
10865	Lepr	leptin receptor	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20181227	MGI			
10865	Lepr	leptin receptor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20190110	MGI			
10865	Lepr	leptin receptor	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20170105	MGI			
10865	Lepr	leptin receptor	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
10865	Lepr	leptin receptor	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10708583
10865	Lepr	leptin receptor	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5918576
10865	Lepr	leptin receptor	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685168
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21745644
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5918576
10865	Lepr	leptin receptor	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150780
10865	Lepr	leptin receptor	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150780
10865	Lepr	leptin receptor	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20181227	MGI			
10865	Lepr	leptin receptor	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20181227	MGI			
10865	Lepr	leptin receptor	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20181227	MGI			
10865	Lepr	leptin receptor	gene	MP:0001525	impaired balance		IEA		N	RGD:5509061	20190110	MGI			
10865	Lepr	leptin receptor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540618
10865	Lepr	leptin receptor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21346177
10865	Lepr	leptin receptor	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685168
10865	Lepr	leptin receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8177042
10865	Lepr	leptin receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8177042
10865	Lepr	leptin receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10708583
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602618
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730408
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685168
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15885672
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16113078
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22609345
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332968
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8177042
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20150416	MGI			PMID:25157166
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20241226	MGI			PMID:38987239
10865	Lepr	leptin receptor	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416008
10865	Lepr	leptin receptor	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
10865	Lepr	leptin receptor	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:760211
10865	Lepr	leptin receptor	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023554
10865	Lepr	leptin receptor	gene	MP:0001727	abnormal embryo implantation		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
10865	Lepr	leptin receptor	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070774
10865	Lepr	leptin receptor	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10708583
10865	Lepr	leptin receptor	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:10708583
10865	Lepr	leptin receptor	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:5918576
10865	Lepr	leptin receptor	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023554
10865	Lepr	leptin receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20190905	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0001868	ovary inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150780
10865	Lepr	leptin receptor	gene	MP:0001922	reduced male fertility		IEA		N	RGD:5509061	20160721	MGI			
10865	Lepr	leptin receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
10865	Lepr	leptin receptor	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0001927	abnormal estrous cycle		IEA		N	RGD:5509061	20120119	MGI			
10865	Lepr	leptin receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
10865	Lepr	leptin receptor	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150780
10865	Lepr	leptin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416008
10865	Lepr	leptin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502493
10865	Lepr	leptin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540618
10865	Lepr	leptin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10708583
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602618
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502493
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730408
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070774
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685168
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15885672
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16113078
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21745644
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22055502
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22414803
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:5918576
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9845674
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20150416	MGI			PMID:25157166
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
10865	Lepr	leptin receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660043
10865	Lepr	leptin receptor	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540618
10865	Lepr	leptin receptor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
10865	Lepr	leptin receptor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602618
10865	Lepr	leptin receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207242
10865	Lepr	leptin receptor	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150780
10865	Lepr	leptin receptor	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21745644
10865	Lepr	leptin receptor	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0002306	abnormal functional residual capacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0002314	abnormal respiratory mechanics		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0002333	abnormal lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434755
10865	Lepr	leptin receptor	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380490
10865	Lepr	leptin receptor	gene	MP:0002497	increased IgE level		IEA		N	RGD:5509061	20161201	MGI			
10865	Lepr	leptin receptor	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023554
10865	Lepr	leptin receptor	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20190905	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20181227	MGI			
10865	Lepr	leptin receptor	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20170105	MGI			
10865	Lepr	leptin receptor	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12885755
10865	Lepr	leptin receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602618
10865	Lepr	leptin receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21346177
10865	Lepr	leptin receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15309293
10865	Lepr	leptin receptor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0002680	decreased corpora lutea number		IEA		N	RGD:5509061	20111116	MGI			
10865	Lepr	leptin receptor	gene	MP:0002682	decreased mature ovarian follicle number		IEA		N	RGD:5509061	20111116	MGI			
10865	Lepr	leptin receptor	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10865	Lepr	leptin receptor	gene	MP:0002710	increased glucagon secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:393618
10865	Lepr	leptin receptor	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0002716	small male preputial gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15309293
10865	Lepr	leptin receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
10865	Lepr	leptin receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17415414
10865	Lepr	leptin receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9299565
10865	Lepr	leptin receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20151126	MGI			PMID:25353183
10865	Lepr	leptin receptor	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20190110	MGI			
10865	Lepr	leptin receptor	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043866
10865	Lepr	leptin receptor	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932425
10865	Lepr	leptin receptor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20201022	MGI			
10865	Lepr	leptin receptor	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17095713
10865	Lepr	leptin receptor	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
10865	Lepr	leptin receptor	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
10865	Lepr	leptin receptor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
10865	Lepr	leptin receptor	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
10865	Lepr	leptin receptor	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22609345
10865	Lepr	leptin receptor	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21745644
10865	Lepr	leptin receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:5009970
10865	Lepr	leptin receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
10865	Lepr	leptin receptor	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:29551634
10865	Lepr	leptin receptor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
10865	Lepr	leptin receptor	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15885672
10865	Lepr	leptin receptor	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103808
10865	Lepr	leptin receptor	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20852026
10865	Lepr	leptin receptor	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103808
10865	Lepr	leptin receptor	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20170105	MGI			
10865	Lepr	leptin receptor	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101849
10865	Lepr	leptin receptor	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540618
10865	Lepr	leptin receptor	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360690
10865	Lepr	leptin receptor	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332968
10865	Lepr	leptin receptor	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20151203	MGI			PMID:24024119
10865	Lepr	leptin receptor	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6991317
10865	Lepr	leptin receptor	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685168
10865	Lepr	leptin receptor	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16522636
10865	Lepr	leptin receptor	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20151126	MGI			PMID:25353183
10865	Lepr	leptin receptor	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201022	MGI			
10865	Lepr	leptin receptor	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20191128	MGI			PMID:29551634
10865	Lepr	leptin receptor	gene	MP:0003819	increased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6991317
10865	Lepr	leptin receptor	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8177042
10865	Lepr	leptin receptor	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416008
10865	Lepr	leptin receptor	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084451
10865	Lepr	leptin receptor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20190905	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0004120	cardiac ischemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540618
10865	Lepr	leptin receptor	gene	MP:0004183	abnormal sympathetic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103808
10865	Lepr	leptin receptor	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5009970
10865	Lepr	leptin receptor	gene	MP:0004195	abnormal kidney calyx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5009970
10865	Lepr	leptin receptor	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20151126	MGI			PMID:25353183
10865	Lepr	leptin receptor	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20190110	MGI			
10865	Lepr	leptin receptor	gene	MP:0004514	dystocia		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
10865	Lepr	leptin receptor	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250911	MGI			PMID:12885755
10865	Lepr	leptin receptor	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:6339122
10865	Lepr	leptin receptor	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21346177
10865	Lepr	leptin receptor	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17095713
10865	Lepr	leptin receptor	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502493
10865	Lepr	leptin receptor	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502493
10865	Lepr	leptin receptor	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16549076
10865	Lepr	leptin receptor	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20201022	MGI			
10865	Lepr	leptin receptor	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380490
10865	Lepr	leptin receptor	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
10865	Lepr	leptin receptor	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
10865	Lepr	leptin receptor	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21393862
10865	Lepr	leptin receptor	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084451
10865	Lepr	leptin receptor	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8177042
10865	Lepr	leptin receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8177042
10865	Lepr	leptin receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685168
10865	Lepr	leptin receptor	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20852026
10865	Lepr	leptin receptor	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730408
10865	Lepr	leptin receptor	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685168
10865	Lepr	leptin receptor	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0005257	abnormal intraocular pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532192
10865	Lepr	leptin receptor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20375117
10865	Lepr	leptin receptor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101849
10865	Lepr	leptin receptor	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
10865	Lepr	leptin receptor	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20151203	MGI			PMID:24024119
10865	Lepr	leptin receptor	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
10865	Lepr	leptin receptor	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9299565
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416008
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070774
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22055502
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22414803
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20151126	MGI			PMID:25353183
10865	Lepr	leptin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
10865	Lepr	leptin receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5009970
10865	Lepr	leptin receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
10865	Lepr	leptin receptor	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540618
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20852026
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21346177
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22414803
10865	Lepr	leptin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20151203	MGI			PMID:24024119
10865	Lepr	leptin receptor	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540618
10865	Lepr	leptin receptor	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207242
10865	Lepr	leptin receptor	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16919419
10865	Lepr	leptin receptor	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17415414
10865	Lepr	leptin receptor	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:6991317
10865	Lepr	leptin receptor	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6991317
10865	Lepr	leptin receptor	gene	MP:0005431	decreased oocyte number		IEA		N	RGD:5509061	20111222	MGI			
10865	Lepr	leptin receptor	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9299565
10865	Lepr	leptin receptor	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0005451	abnormal body composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602618
10865	Lepr	leptin receptor	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416008
10865	Lepr	leptin receptor	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20241226	MGI			PMID:38987239
10865	Lepr	leptin receptor	gene	MP:0005457	abnormal percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12136396
10865	Lepr	leptin receptor	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685168
10865	Lepr	leptin receptor	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0005535	abnormal body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0005540	decreased urine albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12651605
10865	Lepr	leptin receptor	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043866
10865	Lepr	leptin receptor	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0005557	increased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12651605
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416008
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502493
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070774
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16919419
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22414803
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:5918576
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6991317
10865	Lepr	leptin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9845674
10865	Lepr	leptin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15309293
10865	Lepr	leptin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
10865	Lepr	leptin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360690
10865	Lepr	leptin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9299565
10865	Lepr	leptin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
10865	Lepr	leptin receptor	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
10865	Lepr	leptin receptor	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20170105	MGI			
10865	Lepr	leptin receptor	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
10865	Lepr	leptin receptor	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0005576	decreased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0005580	periinsulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
10865	Lepr	leptin receptor	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20210415	MGI			PMID:32233916
10865	Lepr	leptin receptor	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
10865	Lepr	leptin receptor	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20190905	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0005661	decreased circulating adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103808
10865	Lepr	leptin receptor	gene	MP:0005664	decreased circulating noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103808
10865	Lepr	leptin receptor	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
10865	Lepr	leptin receptor	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17415414
10865	Lepr	leptin receptor	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666131
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602618
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070774
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207242
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20086094
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084451
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9845674
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20151126	MGI			PMID:25353183
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20151203	MGI			PMID:24024119
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20241212	MGI			PMID:36243005
10865	Lepr	leptin receptor	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540618
10865	Lepr	leptin receptor	gene	MP:0006315	abnormal urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986513
10865	Lepr	leptin receptor	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207242
10865	Lepr	leptin receptor	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691291
10865	Lepr	leptin receptor	gene	MP:0006353	increased glycosylated hemoglobin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16113078
10865	Lepr	leptin receptor	gene	MP:0006353	increased glycosylated hemoglobin level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0008295	abnormal adrenal gland zona reticularis morphology		IEA		N	RGD:5509061	20111116	MGI			
10865	Lepr	leptin receptor	gene	MP:0008329	decreased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084451
10865	Lepr	leptin receptor	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660043
10865	Lepr	leptin receptor	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150780
10865	Lepr	leptin receptor	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023554
10865	Lepr	leptin receptor	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023554
10865	Lepr	leptin receptor	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023554
10865	Lepr	leptin receptor	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
10865	Lepr	leptin receptor	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
10865	Lepr	leptin receptor	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21346177
10865	Lepr	leptin receptor	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170119	MGI			PMID:22510882
10865	Lepr	leptin receptor	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20241212	MGI			PMID:36243005
10865	Lepr	leptin receptor	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21393862
10865	Lepr	leptin receptor	gene	MP:0008902	abnormal renal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207242
10865	Lepr	leptin receptor	gene	MP:0008902	abnormal renal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0008903	abnormal mesenteric fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207242
10865	Lepr	leptin receptor	gene	MP:0008903	abnormal mesenteric fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0008962	abnormal carbon dioxide production		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20161027	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0009010	abnormal diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0009019	abnormal metestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:378276
10865	Lepr	leptin receptor	gene	MP:0009021	absent estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594516
10865	Lepr	leptin receptor	gene	MP:0009021	absent estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10865	Lepr	leptin receptor	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22414803
10865	Lepr	leptin receptor	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
10865	Lepr	leptin receptor	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6993269
10865	Lepr	leptin receptor	gene	MP:0009255	degranulated pancreatic beta cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123339
10865	Lepr	leptin receptor	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17415414
10865	Lepr	leptin receptor	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20068132
10865	Lepr	leptin receptor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20150416	MGI			PMID:25157166
10865	Lepr	leptin receptor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23864684
10865	Lepr	leptin receptor	gene	MP:0009488	abnormal pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955657
10865	Lepr	leptin receptor	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20170330	MGI			PMID:26441241
10865	Lepr	leptin receptor	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20241226	MGI			PMID:38987239
10865	Lepr	leptin receptor	gene	MP:0009673	increased birth weight		IAGP		N	RGD:5509061	20151126	MGI			PMID:25353183
10865	Lepr	leptin receptor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16113078
10865	Lepr	leptin receptor	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22609345
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416008
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602618
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070774
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207242
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084451
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21745644
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:3882910
10865	Lepr	leptin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20151203	MGI			PMID:24024119
10865	Lepr	leptin receptor	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0010045	increased omental fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
10865	Lepr	leptin receptor	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200402	MGI			
10865	Lepr	leptin receptor	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326958
10865	Lepr	leptin receptor	gene	MP:0010400	increased liver glycogen level		IEA		N	RGD:5509061	20150611	MGI			
10865	Lepr	leptin receptor	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084451
10865	Lepr	leptin receptor	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190110	MGI			
10865	Lepr	leptin receptor	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190110	MGI			
10865	Lepr	leptin receptor	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660043
10865	Lepr	leptin receptor	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540618
10865	Lepr	leptin receptor	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16443782
10865	Lepr	leptin receptor	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20150514	MGI			PMID:25176149
10865	Lepr	leptin receptor	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19582570
10865	Lepr	leptin receptor	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070774
10865	Lepr	leptin receptor	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389315
10865	Lepr	leptin receptor	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015522
10865	Lepr	leptin receptor	gene	MP:0011067	abnormal somatostatin level		IAGP		N	RGD:5509061	20250417	MGI			PMID:337488
10865	Lepr	leptin receptor	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22281595
10865	Lepr	leptin receptor	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0011312	abnormal kidney afferent arteriole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
10865	Lepr	leptin receptor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0011369	increased renal glomerulus apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326220
10865	Lepr	leptin receptor	gene	MP:0011430	mesangiolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10865	Lepr	leptin receptor	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20240509	MGI			PMID:36863097
10865	Lepr	leptin receptor	gene	MP:0011561	renal glomerulus lipidosis		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
10865	Lepr	leptin receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416008
10865	Lepr	leptin receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16423694
10865	Lepr	leptin receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10865	Lepr	leptin receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20151203	MGI			PMID:24024119
10865	Lepr	leptin receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986522
10865	Lepr	leptin receptor	gene	MP:0012008	delayed parturition		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
10865	Lepr	leptin receptor	gene	MP:0012555	decreased cell death		IEA		N	RGD:5509061	20161201	MGI			
10865	Lepr	leptin receptor	gene	MP:0013246	abnormal peptide metabolism		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190110	MGI			
10865	Lepr	leptin receptor	gene	MP:0014121	increased pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20160324	MGI			PMID:19955657
10865	Lepr	leptin receptor	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
10865	Lepr	leptin receptor	gene	MP:0014441	decreased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:11416008
10865	Lepr	leptin receptor	gene	MP:0014441	decreased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:21907138
10865	Lepr	leptin receptor	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20161201	MGI			
10865	Lepr	leptin receptor	gene	MP:0020087	increased susceptibility to non-insulin-dependent diabetes		IAGP		N	RGD:5509061	20150416	MGI			PMID:25157166
10865	Lepr	leptin receptor	gene	MP:0020089	increased susceptibility to diet-induced non-insulin dependent diabetes		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170202	MGI			PMID:23119079
10865	Lepr	leptin receptor	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20171012	MGI			PMID:15309293
10865	Lepr	leptin receptor	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:823065
10865	Lepr	leptin receptor	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:823065
10865	Lepr	leptin receptor	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:16373670
10865	Lepr	leptin receptor	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:22118645
10865	Lepr	leptin receptor	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20231116	MGI			PMID:34390703
10865	Lepr	leptin receptor	gene	MP:0031419	delayed estrus		IAGP		N	RGD:5509061	20220630	MGI			PMID:24024119
10865	Lepr	leptin receptor	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:21346177
10865	Lepr	leptin receptor	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:23119079
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18282810
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18282810
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18282810
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10868	Lgals9	lectin, galactose binding, soluble 9	gene	MP:0020155	enhanced humoral immune response		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
10869	Lhb	luteinizing hormone beta	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0002774	small prostate gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0002779	abnormal sex gland secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0003527	small vulva		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0008258	thin endometrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0009202	small external male genitalia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0009363	abnormal tertiary ovarian follicle morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0013602	abnormal Leydig cell differentiation		IAGP		N	RGD:5509061	20150319	MGI			PMID:17350160
10869	Lhb	luteinizing hormone beta	gene	MP:0013737	small bulbourethral gland		IAGP		N	RGD:5509061	20150416	MGI			PMID:15569941
10869	Lhb	luteinizing hormone beta	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:17350160
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20160811	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000664	small prostate gland anterior lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000671	bulbourethral gland hypoplasia		IAGP		N	RGD:5509061	20150416	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20160811	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20160811	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20160811	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001142	abnormal vagina orifice morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001378	abnormal ejaculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20160811	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002254	reproductive system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12604639
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12604639
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12604639
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002691	small stomach		IEA		N	RGD:5509061	20160811	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002774	small prostate gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002785	absent Leydig cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0002997	enlarged seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0003378	early sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0003531	abnormal vagina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0003596	epididymis inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0003608	prostate gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0003611	scrotum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0003611	scrotum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0003641	small lung		IEA		N	RGD:5509061	20160811	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004909	increased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004928	increased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004932	epididymis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004932	epididymis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12604639
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004958	enlarged prostate gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0004961	increased prostate gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005147	prostate gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005147	prostate gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005148	seminal vesicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005148	seminal vesicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005188	small penis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005188	small penis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005188	small penis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0008257	thin myometrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0008258	thin endometrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009021	absent estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009088	thin uterine horn		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009097	absent endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009201	external male genitalia atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0009214	vas deferens hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0011385	abnormal testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0011533	increased urine major urinary protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0013307	increased adrenal gland weight		IAGP		N	RGD:5509061	20150416	MGI			PMID:15514086
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0013604	abnormal adult Leydig cell differentiation		IAGP		N	RGD:5509061	20150319	MGI			PMID:11145749
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0013604	abnormal adult Leydig cell differentiation		IAGP		N	RGD:5509061	20150319	MGI			PMID:23861372
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220421	MGI			PMID:12604639
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0014193	decreased epididymal cell proliferation		IAGP		N	RGD:5509061	20160526	MGI			PMID:12604639
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0014270	decreased ovary secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:11145748
10870	Lhcgr	luteinizing hormone/choriogonadotropin receptor	gene	MP:0031379	ambiguous external female genitalia		IAGP		N	RGD:5509061	20220421	MGI			PMID:11145749
10871	Lipc	lipase C, hepatic type	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7852377
10871	Lipc	lipase C, hepatic type	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10871	Lipc	lipase C, hepatic type	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11906928
10871	Lipc	lipase C, hepatic type	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10871	Lipc	lipase C, hepatic type	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431181
10871	Lipc	lipase C, hepatic type	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10871	Lipc	lipase C, hepatic type	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7852377
10871	Lipc	lipase C, hepatic type	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11906928
10871	Lipc	lipase C, hepatic type	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11906928
10871	Lipc	lipase C, hepatic type	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10871	Lipc	lipase C, hepatic type	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11906928
10871	Lipc	lipase C, hepatic type	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368783
10871	Lipc	lipase C, hepatic type	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431181
10871	Lipc	lipase C, hepatic type	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7852377
10871	Lipc	lipase C, hepatic type	gene	MP:0006084	abnormal circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7852377
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316346
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316346
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316346
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11717312
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11717312
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723498
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001553	abnormal circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316346
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723498
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835327
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835327
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023560
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835327
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199803
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12865325
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835327
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12865325
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12865325
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0003442	decreased circulating glycerol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023560
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20211021	MGI			
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023560
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723498
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023560
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11717312
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723498
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11717312
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023560
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11717312
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835327
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723498
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023560
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835327
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316346
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12865325
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023560
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723498
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835327
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316346
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023560
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11717312
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0008032	abnormal lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835327
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835327
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023560
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316346
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316346
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11717312
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12865325
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:16199803
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11717312
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639158
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0014476	abnormal feces lipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11564684
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0020101	abnormal hepatic glucose production		IAGP		N	RGD:5509061	20190815	MGI			PMID:12865325
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:12865325
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:18335062
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0031417	decreased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:11717312
10872	Lipe	lipase E, hormone sensitive type	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:12835327
10876	Lpl	lipoprotein lipase	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481534
10876	Lpl	lipoprotein lipase	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
10876	Lpl	lipoprotein lipase	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028738
10876	Lpl	lipoprotein lipase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481534
10876	Lpl	lipoprotein lipase	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481534
10876	Lpl	lipoprotein lipase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:15028738
10876	Lpl	lipoprotein lipase	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028738
10876	Lpl	lipoprotein lipase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0003819	increased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0003820	increased left ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481534
10876	Lpl	lipoprotein lipase	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:15028738
10876	Lpl	lipoprotein lipase	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
10876	Lpl	lipoprotein lipase	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481534
10876	Lpl	lipoprotein lipase	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481534
10876	Lpl	lipoprotein lipase	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20220630	MGI			PMID:15028738
10876	Lpl	lipoprotein lipase	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
10876	Lpl	lipoprotein lipase	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
10876	Lpl	lipoprotein lipase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20170907	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675619
10876	Lpl	lipoprotein lipase	gene	MP:0014864	increased circulating chylomicron triglyceride level		IAGP		N	RGD:5509061	20260219	MGI			PMID:7759497
10876	Lpl	lipoprotein lipase	gene	MP:0014998	abnormal glucose metabolism		IAGP		N	RGD:5509061	20260611	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0015001	increased glucose oxidation		IAGP		N	RGD:5509061	20260611	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0030018	increased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:15028738
10876	Lpl	lipoprotein lipase	gene	MP:0030018	increased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:16410253
10876	Lpl	lipoprotein lipase	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:19481534
10876	Lpl	lipoprotein lipase	gene	MP:0031417	decreased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:15028738
10876	Lpl	lipoprotein lipase	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:12569168
10876	Lpl	lipoprotein lipase	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:16410253
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184108
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:8922669
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20250508	MGI			
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8922669
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20141003	MGI			PMID:8922669
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0008221	abnormal hippocampal commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184108
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7862670
10881	Marcks	myristoylated alanine rich protein kinase C substrate	gene	MP:0030178	abnormal scalp morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:8922669
10882	Mal	myelin and lymphocyte protein, T cell differentiation protein	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15337780
10882	Mal	myelin and lymphocyte protein, T cell differentiation protein	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15337780
10883	Mat1a	methionine adenosyltransferase 1A	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320206
10883	Mat1a	methionine adenosyltransferase 1A	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320206
10883	Mat1a	methionine adenosyltransferase 1A	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320206
10883	Mat1a	methionine adenosyltransferase 1A	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320206
10883	Mat1a	methionine adenosyltransferase 1A	gene	MP:0030644	increased circulating methionine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:11320206
10883	Mat1a	methionine adenosyltransferase 1A	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:11320206
10886	Mc5r	melanocortin 5 receptor	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9413988
10886	Mc5r	melanocortin 5 receptor	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
10886	Mc5r	melanocortin 5 receptor	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
10886	Mc5r	melanocortin 5 receptor	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
10886	Mc5r	melanocortin 5 receptor	gene	MP:0001348	abnormal lacrimal gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9413988
10886	Mc5r	melanocortin 5 receptor	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230119	MGI			
10886	Mc5r	melanocortin 5 receptor	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
10886	Mc5r	melanocortin 5 receptor	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9413988
10886	Mc5r	melanocortin 5 receptor	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:14733892
10886	Mc5r	melanocortin 5 receptor	gene	MP:0005238	increased brain size		IEA		N	RGD:5509061	20230119	MGI			
10886	Mc5r	melanocortin 5 receptor	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9413988
10886	Mc5r	melanocortin 5 receptor	gene	MP:0013476	abnormal Harderian gland porphyrin secretion		IAGP		N	RGD:5509061	20150212	MGI			PMID:9413988
10890	Me1	malic enzyme 1, NADP(+)-dependent, cytosolic	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
10890	Me1	malic enzyme 1, NADP(+)-dependent, cytosolic	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270708
10890	Me1	malic enzyme 1, NADP(+)-dependent, cytosolic	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200402	MGI			
10890	Me1	malic enzyme 1, NADP(+)-dependent, cytosolic	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
10890	Me1	malic enzyme 1, NADP(+)-dependent, cytosolic	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270708
10890	Me1	malic enzyme 1, NADP(+)-dependent, cytosolic	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7276516
10890	Me1	malic enzyme 1, NADP(+)-dependent, cytosolic	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
10891	Vps35	VPS35 retromer complex component	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
10891	Vps35	VPS35 retromer complex component	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20151119	MGI			PMID:26203154
10891	Vps35	VPS35 retromer complex component	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20230511	MGI			PMID:33257649
10891	Vps35	VPS35 retromer complex component	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20200514	MGI			
10891	Vps35	VPS35 retromer complex component	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
10891	Vps35	VPS35 retromer complex component	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20151119	MGI			PMID:26203154
10891	Vps35	VPS35 retromer complex component	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0002922	decreased post-tetanic potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20151119	MGI			PMID:26203154
10891	Vps35	VPS35 retromer complex component	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20151119	MGI			PMID:26203154
10891	Vps35	VPS35 retromer complex component	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20230511	MGI			PMID:33257649
10891	Vps35	VPS35 retromer complex component	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20151119	MGI			PMID:26203154
10891	Vps35	VPS35 retromer complex component	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20230511	MGI			PMID:33257649
10891	Vps35	VPS35 retromer complex component	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20151119	MGI			PMID:26203154
10891	Vps35	VPS35 retromer complex component	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20151119	MGI			PMID:26203154
10891	Vps35	VPS35 retromer complex component	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0008837	increased transforming growth factor beta level		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
10891	Vps35	VPS35 retromer complex component	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20160304	MGI			PMID:24130821
10891	Vps35	VPS35 retromer complex component	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105352
10891	Vps35	VPS35 retromer complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10891	Vps35	VPS35 retromer complex component	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20230511	MGI			PMID:33257649
10891	Vps35	VPS35 retromer complex component	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20221117	MGI			PMID:33745227
10891	Vps35	VPS35 retromer complex component	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20230511	MGI			PMID:33257649
10891	Vps35	VPS35 retromer complex component	gene	MP:0013219	abnormal substantia nigra pars compacta morphology		IAGP		N	RGD:5509061	20230511	MGI			PMID:33257649
10891	Vps35	VPS35 retromer complex component	gene	MP:0020211	slow movement		IAGP		N	RGD:5509061	20230511	MGI			PMID:33257649
10891	Vps35	VPS35 retromer complex component	gene	MP:0020874	abnormal nervous system dopamine level		IAGP		N	RGD:5509061	20221117	MGI			PMID:30155515
10892	Mep1a	meprin 1 alpha	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19262505
10892	Mep1a	meprin 1 alpha	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
10892	Mep1a	meprin 1 alpha	gene	MP:0005265	abnormal blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0005328	abnormal circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0005502	abnormal renal/urinary system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19262505
10892	Mep1a	meprin 1 alpha	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19262505
10892	Mep1a	meprin 1 alpha	gene	MP:0008640	abnormal circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19262505
10892	Mep1a	meprin 1 alpha	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19262505
10892	Mep1a	meprin 1 alpha	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19262505
10892	Mep1a	meprin 1 alpha	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0009646	urinary bladder inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
10892	Mep1a	meprin 1 alpha	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
10892	Mep1a	meprin 1 alpha	gene	MP:0011352	proximal convoluted tubule brush border loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10892	Mep1a	meprin 1 alpha	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
10893	Mep1b	meprin 1 beta	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556482
10893	Mep1b	meprin 1 beta	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
10893	Mep1b	meprin 1 beta	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172000
10893	Mep1b	meprin 1 beta	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556482
10893	Mep1b	meprin 1 beta	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172000
10893	Mep1b	meprin 1 beta	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172000
10893	Mep1b	meprin 1 beta	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172000
10893	Mep1b	meprin 1 beta	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971209
10893	Mep1b	meprin 1 beta	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172000
10893	Mep1b	meprin 1 beta	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556482
10893	Mep1b	meprin 1 beta	gene	MP:0011352	proximal convoluted tubule brush border loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172000
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12397180
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388344
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38438594
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12397180
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000860	abnormal primary somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21195751
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813676
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813676
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001051	abnormal somatic motor system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813676
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17583691
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20180927	MGI			PMID:29999500
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12397180
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813676
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20180927	MGI			PMID:29999500
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21195751
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29999500
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388344
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427375
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427375
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388344
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003326	liver failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388344
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427375
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813676
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388344
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21195751
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21195751
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004170	abnormal orbitofrontal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21195751
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004197	abnormal fetal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004266	pale placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813676
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0004846	absent skeletal muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653949
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427375
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427375
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249655
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427375
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427375
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20240808	MGI			PMID:38438594
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21195751
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12397180
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12397180
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9331067
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17583691
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12397180
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427375
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0011883	absent diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898205
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0012043	increased myoepithelioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557554
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:17923692
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20160915	MGI			PMID:15070743
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0030208	abnormal intrinsic tongue muscle morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:7651534
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0030945	abnormal myoblast migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:11430831
10894	Met	met proto-oncogene, receptor tyrosine kinase	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:15249655
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155946
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155946
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834428
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195353
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638889
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155946
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638889
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155946
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834428
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195353
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723547
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275924
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941270
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834428
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195353
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240116
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941270
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638889
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834428
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240116
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638889
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638889
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240116
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834428
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275924
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723547
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20151119	MGI			PMID:23443560
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723547
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0004934	epididymis epithelium degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240116
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155946
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275924
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195353
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275924
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0008119	decreased Langerhans cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638889
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155946
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16195353
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0009824	spermatic granuloma		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240116
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638889
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0013148	mastitis		IAGP		N	RGD:5509061	20150730	MGI			PMID:16195353
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20150611	MGI			PMID:16275924
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0014347	increased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:15155946
10895	Mfge8	milk fat globule EGF and factor V/VIII domain containing	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:12941270
10896	Mgmt	O-6-methylguanine-DNA methyltransferase	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560238
10896	Mgmt	O-6-methylguanine-DNA methyltransferase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560238
10896	Mgmt	O-6-methylguanine-DNA methyltransferase	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098815
10896	Mgmt	O-6-methylguanine-DNA methyltransferase	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098815
10896	Mgmt	O-6-methylguanine-DNA methyltransferase	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20241121	MGI			
10896	Mgmt	O-6-methylguanine-DNA methyltransferase	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560238
10896	Mgmt	O-6-methylguanine-DNA methyltransferase	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
10896	Mgmt	O-6-methylguanine-DNA methyltransferase	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098815
10896	Mgmt	O-6-methylguanine-DNA methyltransferase	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9560238
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676560
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7333462
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773604
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773604
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676560
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:5786866
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:7333462
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:5786866
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:7333462
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0001309	hydropic eye lens fibers		IEA		N	RGD:5509061	20111116	MGI			
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1026873
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676560
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5716581
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5786866
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7333462
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676560
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773604
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0005545	abnormal lens development		IEA		N	RGD:5509061	20141003	MGI			
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:7333462
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0011697	lens vacuoles		IEA		N	RGD:5509061	20141003	MGI			
10898	Mip	major intrinsic protein of lens fiber	gene	MP:0031345	developmental cataract		IAGP		N	RGD:5509061	20220217	MGI			PMID:12676560
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000017	big ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618927
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674806
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000448	pointed snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371367
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393173
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516260
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:24122813
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393173
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516260
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674806
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:24122813
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:24122813
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934123
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674806
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:24040009
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:24040009
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393173
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18977325
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674806
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24122813
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393173
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516260
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674806
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24122813
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393173
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24040009
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24122813
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24040009
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674806
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004049	increased acute promyelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516260
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004569	glossopharyngeal nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934123
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618927
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618927
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371367
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371367
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24040009
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393173
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0005649	increased spleen neoplasm incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371367
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371367
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371367
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0009879	abnormal arcus anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618927
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0009879	abnormal arcus anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934123
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19212323
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934123
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635450
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516260
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24122813
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16981007
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18977325
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24040009
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477409
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11536426
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371366
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670200
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371367
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674806
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934123
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0012284	increased sternebra number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618927
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0013176	abnormal tail position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20170921	MGI			PMID:16551973
10900	Kmt2a	lysine (K)-specific methyltransferase 2A	gene	MP:0030956	abnormal neuronal precursor cell migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:19212323
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522908
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522908
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20181227	MGI			
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522908
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9508784
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591662
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522908
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20181227	MGI			
10905	Mmp11	matrix metallopeptidase 11	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20211021	MGI			
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769909
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617617
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617617
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9769324
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397239
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9037065
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19002110
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15618213
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923522
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642592
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19002110
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20250925	MGI			PMID:9037065
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642592
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0003901	abnormal PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769909
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617617
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:12045257
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0006142	abnormal sinoatrial node conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769909
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617617
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642592
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617617
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12506066
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769909
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617617
10906	Mmp7	matrix metallopeptidase 7	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676849
10908	Mobp	myelin-associated oligodendrocytic basic protein	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10103078
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641296
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483694
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641296
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483694
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641296
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483694
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641296
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641296
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483694
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641296
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641296
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641296
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624757
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483694
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0004143	muscle hypertonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483694
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624757
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483694
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925695
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237080
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21068410
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20150806	MGI			PMID:19487416
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624757
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624757
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483694
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624757
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624757
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0010205	abnormal oligodendrocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21068410
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0030987	spinal cord inflammation		IAGP		N	RGD:5509061	20191128	MGI			PMID:18641296
10909	Mog	myelin oligodendrocyte glycoprotein	gene	MP:0030991	optic nerve inflammation		IAGP		N	RGD:5509061	20191128	MGI			PMID:18641296
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015609
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015610
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692939
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015610
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015609
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015610
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015609
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015610
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220811	MGI			
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20221215	MGI			
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015609
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015610
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692939
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0009443	parthenogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692939
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069114
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015609
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692939
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0012736	abnormal polar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8015609
10910	Mos	Mos proto-oncogene, serine/threonine kinase	gene	MP:0012737	abnormal primary polar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692939
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098815
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463841
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633693
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098815
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463841
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463841
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098815
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098815
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463841
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463841
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463841
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633693
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9742100
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098815
10914	Mpg	N-methylpurine-DNA glycosylase	gene	MP:0009488	abnormal pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463841
10915	Mpi	mannose phosphate isomerase	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
10915	Mpi	mannose phosphate isomerase	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20141003	MGI			
10915	Mpi	mannose phosphate isomerase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339137
10915	Mpi	mannose phosphate isomerase	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:16339137
10916	Mpo	myeloperoxidase	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181641
10916	Mpo	myeloperoxidase	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16266986
10916	Mpo	myeloperoxidase	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085024
10916	Mpo	myeloperoxidase	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181641
10916	Mpo	myeloperoxidase	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790660
10916	Mpo	myeloperoxidase	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790660
10916	Mpo	myeloperoxidase	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11108938
10916	Mpo	myeloperoxidase	gene	MP:0005044	sepsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593004
10916	Mpo	myeloperoxidase	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790660
10916	Mpo	myeloperoxidase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085024
10916	Mpo	myeloperoxidase	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181641
10916	Mpo	myeloperoxidase	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15911707
10916	Mpo	myeloperoxidase	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085024
10916	Mpo	myeloperoxidase	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181641
10916	Mpo	myeloperoxidase	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16266986
10916	Mpo	myeloperoxidase	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181641
10916	Mpo	myeloperoxidase	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593004
10917	Mpz	myelin protein zero	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12616486
10917	Mpz	myelin protein zero	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:1384988
10917	Mpz	myelin protein zero	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219655
10917	Mpz	myelin protein zero	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:1384988
10917	Mpz	myelin protein zero	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12616486
10917	Mpz	myelin protein zero	gene	MP:0000755	hindlimb paralysis		IEA		N	RGD:5509061	20111116	MGI			
10917	Mpz	myelin protein zero	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266447
10917	Mpz	myelin protein zero	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581451
10917	Mpz	myelin protein zero	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20190221	MGI			PMID:16495463
10917	Mpz	myelin protein zero	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
10917	Mpz	myelin protein zero	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20190221	MGI			PMID:16495463
10917	Mpz	myelin protein zero	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1384988
10917	Mpz	myelin protein zero	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20181227	MGI			
10917	Mpz	myelin protein zero	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20181227	MGI			
10917	Mpz	myelin protein zero	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190124	MGI			PMID:30239779
10917	Mpz	myelin protein zero	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190221	MGI			PMID:16495463
10917	Mpz	myelin protein zero	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12616486
10917	Mpz	myelin protein zero	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:1384988
10917	Mpz	myelin protein zero	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219655
10917	Mpz	myelin protein zero	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:1384988
10917	Mpz	myelin protein zero	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219655
10917	Mpz	myelin protein zero	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:1384988
10917	Mpz	myelin protein zero	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0001924	infertility		IEA		N	RGD:5509061	20111116	MGI			
10917	Mpz	myelin protein zero	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
10917	Mpz	myelin protein zero	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20111116	MGI			
10917	Mpz	myelin protein zero	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
10917	Mpz	myelin protein zero	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20111116	MGI			
10917	Mpz	myelin protein zero	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
10917	Mpz	myelin protein zero	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12616486
10917	Mpz	myelin protein zero	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
10917	Mpz	myelin protein zero	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:1384988
10917	Mpz	myelin protein zero	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:16495463
10917	Mpz	myelin protein zero	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:11086005
10917	Mpz	myelin protein zero	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
10917	Mpz	myelin protein zero	gene	MP:0004263	abnormal limb posture		IEA		N	RGD:5509061	20181011	MGI			
10917	Mpz	myelin protein zero	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20190221	MGI			PMID:16495463
10917	Mpz	myelin protein zero	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581451
10917	Mpz	myelin protein zero	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20190221	MGI			PMID:16495463
10917	Mpz	myelin protein zero	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
10917	Mpz	myelin protein zero	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12616486
10917	Mpz	myelin protein zero	gene	MP:0008243	abnormal macrophage derived foam cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
10917	Mpz	myelin protein zero	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
10917	Mpz	myelin protein zero	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20190221	MGI			PMID:16495463
10917	Mpz	myelin protein zero	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20190228	MGI			PMID:11086005
10917	Mpz	myelin protein zero	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
10917	Mpz	myelin protein zero	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
10917	Mpz	myelin protein zero	gene	MP:0010742	increased Schwann cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10632602
10917	Mpz	myelin protein zero	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266447
10917	Mpz	myelin protein zero	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20190221	MGI			PMID:16495463
10917	Mpz	myelin protein zero	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20190228	MGI			PMID:11086005
10917	Mpz	myelin protein zero	gene	MP:0011906	increased Schwann cell proliferation		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0012674	tomacula		IAGP		N	RGD:5509061	20190228	MGI			PMID:11086005
10917	Mpz	myelin protein zero	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
10917	Mpz	myelin protein zero	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20190124	MGI			PMID:30239779
10917	Mpz	myelin protein zero	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20190221	MGI			PMID:16495463
10917	Mpz	myelin protein zero	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20190228	MGI			PMID:11086005
10917	Mpz	myelin protein zero	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20180809	MGI			PMID:22689911
10917	Mpz	myelin protein zero	gene	MP:0020452	abnormal axon radial sorting		IAGP		N	RGD:5509061	20190124	MGI			PMID:30239779
10918	Mras	muscle and microspikes RAS	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
10918	Mras	muscle and microspikes RAS	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
10918	Mras	muscle and microspikes RAS	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980617
10918	Mras	muscle and microspikes RAS	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
10918	Mras	muscle and microspikes RAS	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
10918	Mras	muscle and microspikes RAS	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
10918	Mras	muscle and microspikes RAS	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20141003	MGI			
10918	Mras	muscle and microspikes RAS	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20230119	MGI			
10918	Mras	muscle and microspikes RAS	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
10919	Abcc1	ATP-binding cassette, sub-family C member 1	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21881209
10919	Abcc1	ATP-binding cassette, sub-family C member 1	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393741
10919	Abcc1	ATP-binding cassette, sub-family C member 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359705
10919	Abcc1	ATP-binding cassette, sub-family C member 1	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359705
10919	Abcc1	ATP-binding cassette, sub-family C member 1	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:21881209
10919	Abcc1	ATP-binding cassette, sub-family C member 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359705
10919	Abcc1	ATP-binding cassette, sub-family C member 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9393741
10919	Abcc1	ATP-binding cassette, sub-family C member 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21881209
10919	Abcc1	ATP-binding cassette, sub-family C member 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359705
10921	Msx2	msh homeobox 2	gene	MP:0000017	big ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12701100
10921	Msx2	msh homeobox 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654563
10921	Msx2	msh homeobox 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597577
10921	Msx2	msh homeobox 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000126	brittle teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000127	degenerate molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000129	ameloblast degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:18667074
10921	Msx2	msh homeobox 2	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:18667074
10921	Msx2	msh homeobox 2	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654563
10921	Msx2	msh homeobox 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0000423	delayed hair regrowth		IEA		N	RGD:5509061	20141003	MGI			
10921	Msx2	msh homeobox 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597577
10921	Msx2	msh homeobox 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
10921	Msx2	msh homeobox 2	gene	MP:0000580	deformed nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
10921	Msx2	msh homeobox 2	gene	MP:0000583	long toenails		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
10921	Msx2	msh homeobox 2	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874124
10921	Msx2	msh homeobox 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0000866	cerebellum vermis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000867	abnormal cerebellum anterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000870	absent cerebellum vermis lobule VIII		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000871	absent cerebellum vermis lobule IX		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874124
10921	Msx2	msh homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20150205	MGI			PMID:24715462
10921	Msx2	msh homeobox 2	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744114
10921	Msx2	msh homeobox 2	gene	MP:0001282	short vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744114
10921	Msx2	msh homeobox 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874124
10921	Msx2	msh homeobox 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20150205	MGI			PMID:24715462
10921	Msx2	msh homeobox 2	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
10921	Msx2	msh homeobox 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090744
10921	Msx2	msh homeobox 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24715462
10921	Msx2	msh homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
10921	Msx2	msh homeobox 2	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874124
10921	Msx2	msh homeobox 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0003110	absent malleus processus brevis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12701100
10921	Msx2	msh homeobox 2	gene	MP:0003110	absent malleus processus brevis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090744
10921	Msx2	msh homeobox 2	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:12701100
10921	Msx2	msh homeobox 2	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
10921	Msx2	msh homeobox 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0004135	abnormal mammary gland embryonic development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0004181	abnormal carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
10921	Msx2	msh homeobox 2	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597577
10921	Msx2	msh homeobox 2	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20171207	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0004575	small limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0004691	absent pubis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12701100
10921	Msx2	msh homeobox 2	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12701100
10921	Msx2	msh homeobox 2	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12701100
10921	Msx2	msh homeobox 2	gene	MP:0006200	vitreous body deposition		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0008372	small malleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12701100
10921	Msx2	msh homeobox 2	gene	MP:0008377	absent malleus manubrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12701100
10921	Msx2	msh homeobox 2	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20150903	MGI			PMID:18667074
10921	Msx2	msh homeobox 2	gene	MP:0008861	abnormal hair shedding		IEA		N	RGD:5509061	20141003	MGI			
10921	Msx2	msh homeobox 2	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090744
10921	Msx2	msh homeobox 2	gene	MP:0009742	increased cornea stroma thickness		IAGP		N	RGD:5509061	20160310	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090744
10921	Msx2	msh homeobox 2	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20150903	MGI			PMID:18667074
10921	Msx2	msh homeobox 2	gene	MP:0010478	intracranial aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
10921	Msx2	msh homeobox 2	gene	MP:0010747	abnormal enamel organ morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930102
10921	Msx2	msh homeobox 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874124
10921	Msx2	msh homeobox 2	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0011513	abnormal vertebral artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
10921	Msx2	msh homeobox 2	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20160310	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0012399	short nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
10921	Msx2	msh homeobox 2	gene	MP:0012401	long nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0012402	abnormal nail bed morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
10921	Msx2	msh homeobox 2	gene	MP:0012403	abnormal nail plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
10921	Msx2	msh homeobox 2	gene	MP:0012405	abnormal nail matrix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
10921	Msx2	msh homeobox 2	gene	MP:0013765	iris hyperplasia		IAGP		N	RGD:5509061	20150430	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0015049	disorganized cerebellar granule layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:22503753
10921	Msx2	msh homeobox 2	gene	MP:0030522	abnormal stellate reticulum morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0030523	abnormal stratum intermedium morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:10742104
10921	Msx2	msh homeobox 2	gene	MP:0030579	thoracoabdominoschisis		IAGP		N	RGD:5509061	20180607	MGI			PMID:18442049
10921	Msx2	msh homeobox 2	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20180726	MGI			PMID:23090744
10921	Msx2	msh homeobox 2	gene	MP:0030992	atrioventricular cushion hypoplasia		IAGP		N	RGD:5509061	20191128	MGI			PMID:18667074
10927	Muc1	mucin 1, transmembrane	gene	MP:0000505	decreased digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719000
10927	Muc1	mucin 1, transmembrane	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638868
10927	Muc1	mucin 1, transmembrane	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20377894
10927	Muc1	mucin 1, transmembrane	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15075252
10927	Muc1	mucin 1, transmembrane	gene	MP:0002830	gallstones		IAGP		N	RGD:5509061	20141003	MGI			PMID:14703511
10927	Muc1	mucin 1, transmembrane	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618757
10927	Muc1	mucin 1, transmembrane	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8530414
10927	Muc1	mucin 1, transmembrane	gene	MP:0005085	abnormal gallbladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14703511
10927	Muc1	mucin 1, transmembrane	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15075252
10927	Muc1	mucin 1, transmembrane	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17638868
10928	Muc2	mucin 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11872843
10928	Muc2	mucin 2	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11872843
10928	Muc2	mucin 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945909
10928	Muc2	mucin 2	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945909
10928	Muc2	mucin 2	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945909
10928	Muc2	mucin 2	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20111116	MGI			
10928	Muc2	mucin 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0001666	abnormal intestinal absorption		IEA		N	RGD:5509061	20111116	MGI			
10928	Muc2	mucin 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945909
10928	Muc2	mucin 2	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11872843
10928	Muc2	mucin 2	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11872843
10928	Muc2	mucin 2	gene	MP:0003292	melena		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945909
10928	Muc2	mucin 2	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11872843
10928	Muc2	mucin 2	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945909
10928	Muc2	mucin 2	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0005036	diarrhea		IEA		N	RGD:5509061	20111116	MGI			
10928	Muc2	mucin 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11872843
10928	Muc2	mucin 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20150319	MGI			PMID:11872843
10928	Muc2	mucin 2	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20150319	MGI			PMID:24945909
10928	Muc2	mucin 2	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160304	MGI			PMID:18318598
10928	Muc2	mucin 2	gene	MP:0014234	decreased enterocyte apoptosis		IAGP		N	RGD:5509061	20230323	MGI			PMID:11872843
10928	Muc2	mucin 2	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20161013	MGI			PMID:18318598
10941	Mycl	Mycl proto-oncogene, bHLH transcription factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8657155
10941	Mycl	Mycl proto-oncogene, bHLH transcription factor	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509714
10941	Mycl	Mycl proto-oncogene, bHLH transcription factor	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509714
10941	Mycl	Mycl proto-oncogene, bHLH transcription factor	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509714
10946	Myf6	myogenic factor 6	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
10946	Myf6	myogenic factor 6	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
10946	Myf6	myogenic factor 6	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7797078
10946	Myf6	myogenic factor 6	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10946	Myf6	myogenic factor 6	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7797078
10946	Myf6	myogenic factor 6	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10946	Myf6	myogenic factor 6	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10946	Myf6	myogenic factor 6	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
10946	Myf6	myogenic factor 6	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18331721
10946	Myf6	myogenic factor 6	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212806
10946	Myf6	myogenic factor 6	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
10946	Myf6	myogenic factor 6	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
10946	Myf6	myogenic factor 6	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
10946	Myf6	myogenic factor 6	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10946	Myf6	myogenic factor 6	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
10946	Myf6	myogenic factor 6	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
10946	Myf6	myogenic factor 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
10946	Myf6	myogenic factor 6	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10946	Myf6	myogenic factor 6	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489287
10946	Myf6	myogenic factor 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
10946	Myf6	myogenic factor 6	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
10946	Myf6	myogenic factor 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489287
10946	Myf6	myogenic factor 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7797078
10946	Myf6	myogenic factor 6	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18331721
10946	Myf6	myogenic factor 6	gene	MP:0003818	abnormal eye muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19531352
10946	Myf6	myogenic factor 6	gene	MP:0003939	abnormal myotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
10946	Myf6	myogenic factor 6	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10946	Myf6	myogenic factor 6	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
10946	Myf6	myogenic factor 6	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626014
10946	Myf6	myogenic factor 6	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10946	Myf6	myogenic factor 6	gene	MP:0004677	truncated ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0004846	absent skeletal muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0005247	abnormal extraocular muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19531352
10946	Myf6	myogenic factor 6	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
10946	Myf6	myogenic factor 6	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10946	Myf6	myogenic factor 6	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
10946	Myf6	myogenic factor 6	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212806
10946	Myf6	myogenic factor 6	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
10946	Myf6	myogenic factor 6	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
10946	Myf6	myogenic factor 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
10946	Myf6	myogenic factor 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18331721
10946	Myf6	myogenic factor 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588068
10946	Myf6	myogenic factor 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
10946	Myf6	myogenic factor 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
10946	Myf6	myogenic factor 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626014
10946	Myf6	myogenic factor 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10946	Myf6	myogenic factor 6	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11715025
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0000741	impaired contractility of urinary bladder detrusor smooth muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0002328	abnormal airway resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959948
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511748
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0003622	ischuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0003624	anuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511748
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511748
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041690
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011095
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10854329
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0012125	decreased bronchoconstrictive response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12959948
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:22511748
10947	Myh11	myosin, heavy polypeptide 11, smooth muscle	gene	MP:0031510	increased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:22511748
10950	Myh3	myosin, heavy polypeptide 3, skeletal muscle, embryonic	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
10950	Myh3	myosin, heavy polypeptide 3, skeletal muscle, embryonic	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
10950	Myh3	myosin, heavy polypeptide 3, skeletal muscle, embryonic	gene	MP:0009405	increased skeletal muscle fiber number		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
10950	Myh3	myosin, heavy polypeptide 3, skeletal muscle, embryonic	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
10950	Myh3	myosin, heavy polypeptide 3, skeletal muscle, embryonic	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
10950	Myh3	myosin, heavy polypeptide 3, skeletal muscle, embryonic	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
10950	Myh3	myosin, heavy polypeptide 3, skeletal muscle, embryonic	gene	MP:0012185	abnormal muscle precursor cell morphology		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
10950	Myh3	myosin, heavy polypeptide 3, skeletal muscle, embryonic	gene	MP:0030972	increased myoblast apoptosis		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
10959	Myo1e	myosin IE	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0000315	hemoglobinuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0002847	abnormal renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22811491
10959	Myo1e	myosin IE	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22811491
10959	Myo1e	myosin IE	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22811491
10959	Myo1e	myosin IE	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:22811491
10959	Myo1e	myosin IE	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
10959	Myo1e	myosin IE	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22811491
10959	Myo1e	myosin IE	gene	MP:0011352	proximal convoluted tubule brush border loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:22811491
10959	Myo1e	myosin IE	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22811491
10959	Myo1e	myosin IE	gene	MP:0011418	leukocyturia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19005011
10959	Myo1e	myosin IE	gene	MP:0011868	podocyte microvillus transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22811491
10960	Myo1c	myosin IC	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23593477
10960	Myo1c	myosin IC	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23593477
10960	Myo1c	myosin IC	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23593477
10960	Myo1c	myosin IC	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23593477
10960	Myo1c	myosin IC	gene	MP:0004438	abnormal vestibular hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102537
10960	Myo1c	myosin IC	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23593477
10960	Myo1c	myosin IC	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23593477
10961	Myo9b	myosin IXb	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566876
10961	Myo9b	myosin IXb	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566876
10961	Myo9b	myosin IXb	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566876
10961	Myo9b	myosin IXb	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566876
10962	Myo5b	myosin VB	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20160407	MGI			PMID:26201991
10962	Myo5b	myosin VB	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:26201991
10962	Myo5b	myosin VB	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26392529
10962	Myo5b	myosin VB	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:26201991
10962	Myo5b	myosin VB	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26392529
10962	Myo5b	myosin VB	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20160407	MGI			PMID:26201991
10962	Myo5b	myosin VB	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:26201991
10962	Myo5b	myosin VB	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20160922	MGI			PMID:26392529
10962	Myo5b	myosin VB	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20160922	MGI			PMID:26392529
10962	Myo5b	myosin VB	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20160407	MGI			PMID:26201991
10962	Myo5b	myosin VB	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20160922	MGI			PMID:26392529
10962	Myo5b	myosin VB	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26392529
10962	Myo5b	myosin VB	gene	MP:0008109	abnormal small intestinal microvillus morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:26201991
10962	Myo5b	myosin VB	gene	MP:0008109	abnormal small intestinal microvillus morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26392529
10962	Myo5b	myosin VB	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160407	MGI			PMID:26201991
10962	Myo5b	myosin VB	gene	MP:0014078	small intestinal villus atrophy		IAGP		N	RGD:5509061	20160922	MGI			PMID:26392529
10962	Myo5b	myosin VB	gene	MP:0014080	fused small intestinal villi		IAGP		N	RGD:5509061	20160922	MGI			PMID:26392529
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000736	delayed muscle development		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20230601	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20220714	MGI			PMID:35075134
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20230601	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20220714	MGI			PMID:35075134
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0002058	neonatal lethality		IEA		N	RGD:5509061	20111116	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0002210	abnormal sex determination		IAGP		N	RGD:5509061	20220714	MGI			PMID:35075134
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20220714	MGI			PMID:35075134
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20220714	MGI			PMID:35075134
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20220714	MGI			PMID:35075134
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20220714	MGI			PMID:35075134
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004445	small exoccipital bone		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004447	small basioccipital bone		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20221215	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20181227	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0005652	sex reversal		IAGP		N	RGD:5509061	20220714	MGI			PMID:35075134
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931680
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18562292
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20220714	MGI			PMID:35075134
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20220714	MGI			PMID:18812566
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0012745	abnormal neural crest cell physiology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0012755	decreased cranial neural crest cell number		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0012761	increased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0014711	decreased synaptic vesicle readily releasable pool size		IAGP		N	RGD:5509061	20250814	MGI			PMID:20159449
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0030049	prominent forehead		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0030320	abnormal temporal bone tympanic part morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:24080509
10967	Nedd4	neural precursor cell expressed, developmentally down-regulated 4	gene	MP:0031458	absent palate bones		IAGP		N	RGD:5509061	20221124	MGI			PMID:24080509
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402469
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9763429
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0000947	convulsive seizures		IEA		N	RGD:5509061	20260402	MGI			
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9763429
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:9763429
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:17005864
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:14662745
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402469
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186852
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14662745
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9763431
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402469
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210520	MGI			
10969	Nefh	neurofilament, heavy polypeptide	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14662745
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402469
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22553027
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22553027
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:17005864
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:14662745
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402469
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14662745
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14662746
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19193875
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566972
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10402469
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14662745
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14662746
10970	Nefm	neurofilament, medium polypeptide	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22553027
10971	Nes	nestin	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832185
10971	Nes	nestin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832185
10971	Nes	nestin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963821
10971	Nes	nestin	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20240523	MGI			
10971	Nes	nestin	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
10971	Nes	nestin	gene	MP:0003631	nervous system phenotype		IAGP		N	RGD:5509061	20230406	MGI			PMID:34739481
10971	Nes	nestin	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963821
10971	Nes	nestin	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
10971	Nes	nestin	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20230406	MGI			PMID:34739481
10971	Nes	nestin	gene	MP:0005380	embryo phenotype		IAGP		N	RGD:5509061	20230406	MGI			PMID:34739481
10971	Nes	nestin	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20250515	MGI			PMID:39977508
10971	Nes	nestin	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963821
10971	Nes	nestin	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963821
10971	Nes	nestin	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963821
10971	Nes	nestin	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963821
10971	Nes	nestin	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963821
10971	Nes	nestin	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:39977508
10972	Neu1	neuraminidase 1	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217813
10972	Neu1	neuraminidase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0003201	extremity edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0003622	ischuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217813
10972	Neu1	neuraminidase 1	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0005060	accumulation of giant lysosomes in kidney/renal tubule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0005567	decreased circulating total protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217813
10972	Neu1	neuraminidase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9363440
10972	Neu1	neuraminidase 1	gene	MP:0006167	eyelid edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10972	Neu1	neuraminidase 1	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217813
10972	Neu1	neuraminidase 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023988
10973	Nf1	neurofibromin 1	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
10973	Nf1	neurofibromin 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10973	Nf1	neurofibromin 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
10973	Nf1	neurofibromin 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
10973	Nf1	neurofibromin 1	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20151001	MGI			PMID:12533510
10973	Nf1	neurofibromin 1	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10973	Nf1	neurofibromin 1	gene	MP:0000597	delayed hepatic development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
10973	Nf1	neurofibromin 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0000736	delayed muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
10973	Nf1	neurofibromin 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:12533510
10973	Nf1	neurofibromin 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0000863	abnormal secondary somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10973	Nf1	neurofibromin 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0000959	abnormal somatic sensory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0001009	paravertebral ganglia hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0001010	prevertebral ganglia hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0001148	enlarged testis		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
10973	Nf1	neurofibromin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0001267	enlarged chest		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
10973	Nf1	neurofibromin 1	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
10973	Nf1	neurofibromin 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896734
10973	Nf1	neurofibromin 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
10973	Nf1	neurofibromin 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
10973	Nf1	neurofibromin 1	gene	MP:0001396	unidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
10973	Nf1	neurofibromin 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11279521
10973	Nf1	neurofibromin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11279521
10973	Nf1	neurofibromin 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9054942
10973	Nf1	neurofibromin 1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
10973	Nf1	neurofibromin 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
10973	Nf1	neurofibromin 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
10973	Nf1	neurofibromin 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10973	Nf1	neurofibromin 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
10973	Nf1	neurofibromin 1	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397217
10973	Nf1	neurofibromin 1	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10973	Nf1	neurofibromin 1	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20160929	MGI			PMID:23858101
10973	Nf1	neurofibromin 1	gene	MP:0002031	increased adrenal gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
10973	Nf1	neurofibromin 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
10973	Nf1	neurofibromin 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
10973	Nf1	neurofibromin 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20160929	MGI			PMID:23858101
10973	Nf1	neurofibromin 1	gene	MP:0002033	increased malignant triton tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20160929	MGI			PMID:23858101
10973	Nf1	neurofibromin 1	gene	MP:0002037	increased fibrohistocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9214616
10973	Nf1	neurofibromin 1	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0002050	increased pheochromocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0002050	increased pheochromocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319471
10973	Nf1	neurofibromin 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
10973	Nf1	neurofibromin 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397217
10973	Nf1	neurofibromin 1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896734
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
10973	Nf1	neurofibromin 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
10973	Nf1	neurofibromin 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
10973	Nf1	neurofibromin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18768391
10973	Nf1	neurofibromin 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
10973	Nf1	neurofibromin 1	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0002802	abnormal discrimination learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11279521
10973	Nf1	neurofibromin 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10973	Nf1	neurofibromin 1	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
10973	Nf1	neurofibromin 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0002999	abnormal bone healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
10973	Nf1	neurofibromin 1	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0003808	increased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0003808	increased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0003834	abnormal adrenergic chromaffin cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
10973	Nf1	neurofibromin 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10973	Nf1	neurofibromin 1	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0004182	abnormal spermiation		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0004309	absent otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0004987	abnormal osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
10973	Nf1	neurofibromin 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
10973	Nf1	neurofibromin 1	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0005646	abnormal pituitary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
10973	Nf1	neurofibromin 1	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
10973	Nf1	neurofibromin 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0008301	adrenal medulla hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0008302	thin adrenal cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20141127	MGI			PMID:18614544
10973	Nf1	neurofibromin 1	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18768391
10973	Nf1	neurofibromin 1	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
10973	Nf1	neurofibromin 1	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896734
10973	Nf1	neurofibromin 1	gene	MP:0009233	enlarged sperm head		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
10973	Nf1	neurofibromin 1	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
10973	Nf1	neurofibromin 1	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
10973	Nf1	neurofibromin 1	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0009460	skeletal muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0009770	abnormal optic chiasm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10973	Nf1	neurofibromin 1	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896734
10973	Nf1	neurofibromin 1	gene	MP:0010050	hypermyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0010160	increased oligodendrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
10973	Nf1	neurofibromin 1	gene	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319471
10973	Nf1	neurofibromin 1	gene	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
10973	Nf1	neurofibromin 1	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
10973	Nf1	neurofibromin 1	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20600672
10973	Nf1	neurofibromin 1	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896734
10973	Nf1	neurofibromin 1	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
10973	Nf1	neurofibromin 1	gene	MP:0010310	increased Schwannoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0010314	increased neurofibroma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
10973	Nf1	neurofibromin 1	gene	MP:0010314	increased neurofibroma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10973	Nf1	neurofibromin 1	gene	MP:0010314	increased neurofibroma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0010314	increased neurofibroma incidence		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0010334	pleural effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0010361	increased gangliosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0010362	increased ganglioneuroma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12469121
10973	Nf1	neurofibromin 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0010614	abnormal mitral valve cusp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0010727	increased glioblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
10973	Nf1	neurofibromin 1	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0010929	increased osteoid thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0010964	increased compact bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22868293
10973	Nf1	neurofibromin 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
10973	Nf1	neurofibromin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371380
10973	Nf1	neurofibromin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151001	MGI			PMID:12533510
10973	Nf1	neurofibromin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190207	MGI			PMID:27482814
10973	Nf1	neurofibromin 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10973	Nf1	neurofibromin 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0011180	abnormal hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982883
10973	Nf1	neurofibromin 1	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20151001	MGI			PMID:12533510
10973	Nf1	neurofibromin 1	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20151001	MGI			PMID:12533510
10973	Nf1	neurofibromin 1	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926784
10973	Nf1	neurofibromin 1	gene	MP:0011746	spleen fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
10973	Nf1	neurofibromin 1	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11297510
10973	Nf1	neurofibromin 1	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0012415	decreased sarcoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
10973	Nf1	neurofibromin 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
10973	Nf1	neurofibromin 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
10973	Nf1	neurofibromin 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7920653
10973	Nf1	neurofibromin 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
10973	Nf1	neurofibromin 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
10973	Nf1	neurofibromin 1	gene	MP:0012761	increased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
10973	Nf1	neurofibromin 1	gene	MP:0013693	abnormal hemopoiesis		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0014049	increased T cell acute lymphoblastic leukemia incidence		IAGP		N	RGD:5509061	20160818	MGI			PMID:26764354
10973	Nf1	neurofibromin 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:10973261
10973	Nf1	neurofibromin 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:15652750
10973	Nf1	neurofibromin 1	gene	MP:0014635	increased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0020355	abnormal Sertoli cell barrier morphology		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0020549	increased optic chiasm size		IAGP		N	RGD:5509061	20180301	MGI			PMID:21896734
10973	Nf1	neurofibromin 1	gene	MP:0030603	increased sperm number		IAGP		N	RGD:5509061	20190404	MGI			PMID:30571760
10973	Nf1	neurofibromin 1	gene	MP:0030947	increased myoblast proliferation		IAGP		N	RGD:5509061	20190725	MGI			PMID:21478499
10973	Nf1	neurofibromin 1	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231102	MGI			PMID:7926784
10974	Nfia	nuclear factor I/A	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514217
10974	Nfia	nuclear factor I/A	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514217
10974	Nfia	nuclear factor I/A	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553984
10974	Nfia	nuclear factor I/A	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553984
10974	Nfia	nuclear factor I/A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553984
10974	Nfia	nuclear factor I/A	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514217
10974	Nfia	nuclear factor I/A	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514217
10974	Nfia	nuclear factor I/A	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553984
10974	Nfia	nuclear factor I/A	gene	MP:0008221	abnormal hippocampal commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514217
10974	Nfia	nuclear factor I/A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0011488	abnormal ureterovesical junction morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10974	Nfia	nuclear factor I/A	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518556
10974	Nfia	nuclear factor I/A	gene	MP:0012545	syringomyelia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17530927
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845452
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845452
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845452
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845452
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665694
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665694
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9743524
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845452
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0002869	increased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665694
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008180	abnormal marginal zone B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665694
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665694
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008638	increased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665694
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696914
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0010674	increased activation-induced B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0010836	decreased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333553
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067893
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845452
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590249
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628301
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665694
10975	Nfkbia	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:8628301
10978	Ngf	nerve growth factor	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19755105
10978	Ngf	nerve growth factor	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:21151121
10978	Ngf	nerve growth factor	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001014	absent superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001015	small superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:30612733
10978	Ngf	nerve growth factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20200213	MGI			PMID:31685654
10978	Ngf	nerve growth factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0001968	abnormal touch/nociception		IAGP		N	RGD:5509061	20200213	MGI			PMID:31685654
10978	Ngf	nerve growth factor	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200213	MGI			PMID:31685654
10978	Ngf	nerve growth factor	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200213	MGI			PMID:31685654
10978	Ngf	nerve growth factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:30612733
10978	Ngf	nerve growth factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31685654
10978	Ngf	nerve growth factor	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19755105
10978	Ngf	nerve growth factor	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30612733
10978	Ngf	nerve growth factor	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10978	Ngf	nerve growth factor	gene	MP:0006408	dorsal root ganglion hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20200213	MGI			PMID:31685654
10978	Ngf	nerve growth factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200213	MGI			PMID:31685654
10978	Ngf	nerve growth factor	gene	MP:0014488	abnormal skin sensory neuron innervation pattern		IAGP		N	RGD:5509061	20240801	MGI			PMID:31685654
10978	Ngf	nerve growth factor	gene	MP:0014488	abnormal skin sensory neuron innervation pattern		IAGP		N	RGD:5509061	20240801	MGI			PMID:8137419
10978	Ngf	nerve growth factor	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:31685654
10978	Ngf	nerve growth factor	gene	MP:0015018	increased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:30612733
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564506
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:1317267
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000578	ulcerated autopod		IAGP		N	RGD:5509061	20141003	MGI			PMID:1317267
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160421	MGI			
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126035
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18786358
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745667
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:1317267
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126035
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:8128229
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268129
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001021	small L4 dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001022	abnormal L5 dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001038	abnormal cholinergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10762318
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126035
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772898
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001107	decreased Schwann cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10762318
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21413144
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21413144
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:1317267
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268129
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20160421	MGI			
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21413144
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11724766
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21413144
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268129
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564506
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17934455
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18786358
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23091165
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003201	extremity edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:1317267
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9472042
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995552
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647357
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032673
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382462
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268129
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0004220	abnormal peripheral nervous system regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745667
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564506
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564506
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564506
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16519950
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242267
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17493809
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133718
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0006070	increased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589782
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0006258	abnormal circumvallate papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126035
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0006260	abnormal gustatory papilla taste bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15126035
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18786358
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0008468	absent muscle spindles		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0008486	decreased muscle spindle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133718
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17934455
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0008960	abnormal axon pruning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382462
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032673
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10188952
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559852
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564506
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20230810	MGI			PMID:9268129
10983	Ngfr	nerve growth factor receptor (TNFR superfamily, member 16)	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
10985	Ninj1	ninjurin 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141009	MGI			PMID:24347169
10985	Ninj1	ninjurin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141009	MGI			PMID:24347169
10985	Ninj1	ninjurin 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690620
10985	Ninj1	ninjurin 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141009	MGI			PMID:24347169
10985	Ninj1	ninjurin 1	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690620
10985	Ninj1	ninjurin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690620
10985	Ninj1	ninjurin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690620
10985	Ninj1	ninjurin 1	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24347169
10985	Ninj1	ninjurin 1	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141009	MGI			PMID:24347169
10985	Ninj1	ninjurin 1	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141009	MGI			PMID:24347169
10985	Ninj1	ninjurin 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141009	MGI			PMID:24347169
10985	Ninj1	ninjurin 1	gene	MP:0008007	abnormal cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690620
10987	Nmbr	neuromedin B receptor	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231437
10987	Nmbr	neuromedin B receptor	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9920658
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20200514	MGI			
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20161216	MGI			PMID:22634753
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16399503
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16804088
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20241121	MGI			
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16399503
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16804088
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20241121	MGI			
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16399503
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0008291	abnormal adrenocortical cell morphology		IAGP		N	RGD:5509061	20161216	MGI			PMID:22634753
10988	Nnt	nicotinamide nucleotide transhydrogenase	gene	MP:0014285	disorganized adrenal gland zona fasciculata		IAGP		N	RGD:5509061	20230907	MGI			PMID:22634753
10989	Nog	noggin	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20063299
10989	Nog	noggin	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201022	MGI			
10989	Nog	noggin	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0000537	abnormal urethra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781691
10989	Nog	noggin	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781691
10989	Nog	noggin	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
10989	Nog	noggin	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
10989	Nog	noggin	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
10989	Nog	noggin	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0002632	vestigial tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0002632	vestigial tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0002759	abnormal caudal vertebrae morphology		IEA		N	RGD:5509061	20220811	MGI			
10989	Nog	noggin	gene	MP:0002770	absent bulbourethral gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
10989	Nog	noggin	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0003125	abnormal septation of the cloaca		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0003130	anal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20063299
10989	Nog	noggin	gene	MP:0003160	abnormal esophagus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0003190	fused synovial joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20230601	MGI			
10989	Nog	noggin	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559902
10989	Nog	noggin	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0003740	fusion of middle ear ossicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210128	MGI			
10989	Nog	noggin	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0003942	abnormal urinary system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
10989	Nog	noggin	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550712
10989	Nog	noggin	gene	MP:0004387	abnormal prechordal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
10989	Nog	noggin	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20063299
10989	Nog	noggin	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20063299
10989	Nog	noggin	gene	MP:0004554	small pharynx		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0004575	small limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0004603	absent vertebral arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134349
10989	Nog	noggin	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
10989	Nog	noggin	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0005315	absent pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0005646	abnormal pituitary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0006291	aprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0006295	absent sclerotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0006295	absent sclerotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0008023	abnormal styloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0008320	absent adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0008926	abnormal anterior definitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
10989	Nog	noggin	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
10989	Nog	noggin	gene	MP:0009570	abnormal right lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781691
10989	Nog	noggin	gene	MP:0009735	abnormal prostate gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0010116	abnormal primitive urogenital sinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0010884	esophagus stenosis		IAGP		N	RGD:5509061	20150319	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
10989	Nog	noggin	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
10989	Nog	noggin	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598734
10989	Nog	noggin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10989	Nog	noggin	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0011361	pelvic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028901
10989	Nog	noggin	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585504
10989	Nog	noggin	gene	MP:0011759	absent Rathke's pouch		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096605
10989	Nog	noggin	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
10989	Nog	noggin	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303853
10989	Nog	noggin	gene	MP:0013351	abnormal Rathke's pouch development		IAGP		N	RGD:5509061	20141218	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0013352	abnormal Rathke's pouch apoptosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0014198	absent pituitary infundibular stalk		IAGP		N	RGD:5509061	20160526	MGI			PMID:17359964
10989	Nog	noggin	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20170921	MGI			PMID:16712836
10989	Nog	noggin	gene	MP:0031362	decreased prostate gland ventral lobe weight		IAGP		N	RGD:5509061	20220303	MGI			PMID:18028901
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297441
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297441
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11920687
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16246868
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9681470
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852587
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727738
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652188
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18852886
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158630
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11235982
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477374
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15158692
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20250206	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351742
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15158692
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15158692
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978606
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12738065
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077313
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155789
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001629	abnormal heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155789
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001664	abnormal digestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982771
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001752	abnormal hypothalamus secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12562678
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:10456061
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505721
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677545
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11992469
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297441
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16246868
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7518615
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10362674
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11709397
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16246868
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652188
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18852886
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003023	decreased coronary flow rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652188
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15158692
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003285	gastric hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982771
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003307	pyloric stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003307	pyloric stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505721
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:9848082
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003434	decreased susceptibility to induced choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11920687
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351742
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10362674
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781920
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381772
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:18852886
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10479702
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003821	decreased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15158692
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:10479702
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982771
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505721
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0003991	arteriosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004036	abnormal muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444441
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004036	abnormal muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677545
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12081996
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004220	abnormal peripheral nervous system regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11992469
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652188
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004495	decreased synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:9692709
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004545	enlarged esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982771
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072412
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10966931
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12397095
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12738065
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381772
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17446423
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005322	abnormal serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158630
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10905473
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005573	increased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005575	increased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005585	increased tidal volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005600	increased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12081996
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16246868
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062295
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7522345
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062295
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852587
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17446423
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8667023
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297441
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008779	abnormal maternal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10479702
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155789
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008962	abnormal carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297441
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:10966931
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009357	abnormal seizure response to inducing agent		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781920
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351742
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351742
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009814	increased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009854	impaired gastric peristalsis		IAGP		N	RGD:5509061	20150702	MGI			PMID:10982771
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12886012
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010017	visceral vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010106	abnormal circulating pyruvate kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9681470
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10966931
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010108	abnormal renal water reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10966931
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297441
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010154	abnormal gastroesophageal sphincter physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444441
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010154	abnormal gastroesophageal sphincter physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438492
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18852886
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010654	slow Wallerian degeneration		IAGP		N	RGD:5509061	20220120	MGI			PMID:11992469
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010781	pyloric sphincter hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982771
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010781	pyloric sphincter hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010781	pyloric sphincter hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505721
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010782	stomach smooth muscle circular layer hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505721
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010783	abnormal stomach wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7505721
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297441
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12704728
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0011462	increased urine bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10966931
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0011508	abnormal glomerular capillary thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0011749	perivascular fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0011882	enlarged duodenum		IAGP		N	RGD:5509061	20150702	MGI			PMID:10982771
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:22522563
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0011988	increased mating frequency		IAGP		N	RGD:5509061	20250206	MGI			PMID:7477374
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20170921	MGI			PMID:10966931
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0020333	enhanced leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:10362674
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0020844	abnormal pulmonary respiratory rate response		IAGP		N	RGD:5509061	20181101	MGI			PMID:9679181
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0031182	abnormal cerebral blood flow rate		IAGP		N	RGD:5509061	20201231	MGI			PMID:12623792
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0031330	delayed peripheral nervous system regeneration		IAGP		N	RGD:5509061	20220120	MGI			PMID:11992469
10991	Nos1	nitric oxide synthase 1, neuronal	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:9848082
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919259
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000199	abnormal circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11369002
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15971084
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11920687
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11435211
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000505	decreased digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719000
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199408
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751989
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20150716	MGI			PMID:18272675
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12090918
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810565
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10975863
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894526
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876161
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12738065
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11369002
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12016261
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001664	abnormal digestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12646421
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886418
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15556608
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886418
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12562678
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886418
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919259
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12562678
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539113
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001881	abnormal mammary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345368
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810565
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12090918
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17206489
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731407
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17206489
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364062
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:11379816
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919259
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879252
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10919259
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11504701
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810565
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15205363
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20150716	MGI			PMID:18272675
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16027239
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7538909
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199408
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10788454
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14617760
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002602	abnormal eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886418
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11254671
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520837
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002733	abnormal thermal nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:11379816
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11590438
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11590438
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12054156
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16460714
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486966
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19443702
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12016261
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0002999	abnormal bone healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894526
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406467
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003177	allodynia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11379816
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003194	abnormal frequency of paradoxical sleep		IAGP		N	RGD:5509061	20141003	MGI			PMID:12738065
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20150716	MGI			PMID:18272675
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11379816
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908860
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:19096157
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908860
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:19096157
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20150716	MGI			PMID:18272675
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15567150
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003434	decreased susceptibility to induced choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11920687
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731407
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17206489
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546953
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17206489
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12054156
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003823	increased left ventricle developed pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509452
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003930	abnormal tooth hard tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15777672
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16631135
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003966	abnormal adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16631135
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10975863
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003991	arteriosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546953
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0003995	abnormal uterine artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12090918
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:10484522
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19096157
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12016261
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004220	abnormal peripheral nervous system regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11379816
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20150716	MGI			PMID:18272675
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004389	abnormal respiratory bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11504701
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989972
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16917077
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9510198
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810565
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10948185
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12054156
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15777672
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15777672
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20220922	MGI			PMID:15777672
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12738065
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886418
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15777672
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539113
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345368
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12016261
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19443702
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810565
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11369002
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005183	abnormal circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377046
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11590438
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11435211
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005316	abnormal response to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:11379816
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682064
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11504701
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12016261
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:10975863
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11369002
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199408
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539113
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005410	abnormal fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087361
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14617760
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539113
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11369002
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682064
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005610	increased circulating antidiuretic hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15971084
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19443702
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15556608
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9364062
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0006141	abnormal atrioventricular node conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12016261
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11369002
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055518
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:20345368
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0006308	enlarged seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810565
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20150611	MGI			PMID:23741483
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199408
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19096157
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:18272675
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008287	abnormal subiculum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19096157
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15777672
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20150716	MGI			PMID:18272675
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19096157
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886418
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665440
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539113
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886418
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:7538909
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539113
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008775	abnormal heart ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12016261
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19096157
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377046
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:10966931
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009548	abnormal platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10788454
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009623	enlarged inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199408
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11369002
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682064
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11254671
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682064
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751989
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009814	increased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:12749913
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:17206489
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0010017	visceral vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:17206489
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12016261
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0010755	abnormal heart right ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10484454
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0010781	pyloric sphincter hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15777672
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0010961	increased compact bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15777672
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12704728
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0011508	abnormal glomerular capillary thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0011564	decreased urine prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10788454
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0011742	decreased urine nitrite level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0011749	perivascular fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:11590438
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0013717	hyperlactation		IAGP		N	RGD:5509061	20150611	MGI			PMID:20345368
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:15777672
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20171012	MGI			PMID:12738065
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0020537	decreased subiculum size		IAGP		N	RGD:5509061	20180301	MGI			PMID:18272675
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0020537	decreased subiculum size		IAGP		N	RGD:5509061	20180301	MGI			PMID:19096157
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220519	MGI			
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0030013	enhanced central nervous system regeneration		IAGP		N	RGD:5509061	20170713	MGI			PMID:15520837
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0030603	increased sperm number		IAGP		N	RGD:5509061	20180621	MGI			PMID:12810565
10996	Nos2	nitric oxide synthase 2, inducible	gene	MP:0031330	delayed peripheral nervous system regeneration		IAGP		N	RGD:5509061	20220120	MGI			PMID:11379816
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16763060
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:11141498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16763060
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781920
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9201025
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10435012
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652188
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:7545787
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:9468189
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9201025
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220804	MGI			PMID:11779605
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699263
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11920687
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843834
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11141498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843834
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15305857
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10727738
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663015
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663015
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588707
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8917564
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964974
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001378	abnormal ejaculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549894
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001379	abnormal penile erection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11904450
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964974
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964974
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978606
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16763060
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467476
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10435012
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9201025
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841206
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663015
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12562678
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964974
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10534440
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15305857
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964974
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843834
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683374
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10785232
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467476
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588707
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11706934
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10362674
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9201025
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663015
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468208
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10484454
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8917564
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15305857
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11141498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210128	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003023	decreased coronary flow rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652188
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10435012
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10484454
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9468189
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003033	abnormal pulmonary vascular resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9201025
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11141498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:16886062
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:11141498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468208
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841206
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8917564
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663015
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:10377046
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003547	abnormal pulmonary pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10484454
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:9201025
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10362674
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781920
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:9201025
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003820	increased left ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841206
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003821	decreased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683374
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467476
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:9692709
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0003991	arteriosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588707
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004044	aortic dissection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468208
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843834
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16763060
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18256327
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821808
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004857	abnormal heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10362674
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468208
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467476
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004877	abnormal systemic vascular resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9201025
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9502763
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9616228
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210128	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15305857
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433298
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11141498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16763060
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468208
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17446423
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377046
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005186	increased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377046
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133872
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005322	abnormal serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964974
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683374
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11141498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467476
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10905473
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10435012
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652188
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467476
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8917564
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9468189
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683374
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683374
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468208
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:16886062
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683374
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467476
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18206129
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10435012
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7545787
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005600	increased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841206
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006057	decreased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683374
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907582
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699263
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467476
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081021
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081021
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8667023
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20151112	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788381
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008823	abnormal interventricular septum membranous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663015
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699263
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008976	delayed female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10785232
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20220804	MGI			PMID:10785232
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377046
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009007	short estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10534440
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377046
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291238
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009345	abnormal trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11141498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009357	abnormal seizure response to inducing agent		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781920
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009641	kidney degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457755
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663015
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009648	abnormal superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:10534440
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009648	abnormal superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:10785232
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133872
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11920687
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663015
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16886062
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11706934
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009814	increased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699263
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010017	visceral vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010180	increased susceptibility to weight loss		IEA		N	RGD:5509061	20151112	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010405	ostium secundum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010483	aortic sinus aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683374
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821808
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010563	increased heart right ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468208
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010755	abnormal heart right ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10484454
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010755	abnormal heart right ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821017
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010755	abnormal heart right ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010781	pyloric sphincter hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010814	absent alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0010894	pulmonary alveolar edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843834
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016731
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12704728
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011312	abnormal kidney afferent arteriole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011392	increased fetal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176963
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011430	mesangiolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971655
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011430	mesangiolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011508	abnormal glomerular capillary thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024729
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011508	abnormal glomerular capillary thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011561	renal glomerulus lipidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200185
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0011749	perivascular fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413498
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0012737	abnormal primary polar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9607805
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231221	MGI			PMID:15350840
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0014368	enhanced long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:10964974
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0015043	increased circulating tartrate resistant acid phosphatase 5 level		IAGP		N	RGD:5509061	20260709	MGI			PMID:16763060
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0020333	enhanced leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:10362674
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0021161	increased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:11468208
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0030984	increased circulating osteocalcin level		IAGP		N	RGD:5509061	20201001	MGI			PMID:16763060
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0031182	abnormal cerebral blood flow rate		IAGP		N	RGD:5509061	20201231	MGI			PMID:12781920
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0031274	increased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20210617	MGI			PMID:11468208
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0031274	increased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20210617	MGI			PMID:19036847
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:10785232
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:11779605
10997	Nos3	nitric oxide synthase 3, endothelial cell	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:9607805
10998	Notch1	notch 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22484060
10998	Notch1	notch 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
10998	Notch1	notch 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17229764
10998	Notch1	notch 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
10998	Notch1	notch 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10879540
10998	Notch1	notch 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17336907
10998	Notch1	notch 1	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095891
10998	Notch1	notch 1	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080428
10998	Notch1	notch 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0000387	disorganized inner root sheath cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0000388	absent hair follicle inner root sheath		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293291
10998	Notch1	notch 1	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0000648	absent sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
10998	Notch1	notch 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
10998	Notch1	notch 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
10998	Notch1	notch 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293291
10998	Notch1	notch 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
10998	Notch1	notch 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17229764
10998	Notch1	notch 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15081359
10998	Notch1	notch 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595837
10998	Notch1	notch 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10879540
10998	Notch1	notch 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
10998	Notch1	notch 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730124
10998	Notch1	notch 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:10879540
10998	Notch1	notch 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10879540
10998	Notch1	notch 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8573724
10998	Notch1	notch 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658279
10998	Notch1	notch 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19110448
10998	Notch1	notch 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17261636
10998	Notch1	notch 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21311046
10998	Notch1	notch 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
10998	Notch1	notch 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595837
10998	Notch1	notch 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595837
10998	Notch1	notch 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16885355
10998	Notch1	notch 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
10998	Notch1	notch 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17261636
10998	Notch1	notch 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19110448
10998	Notch1	notch 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17261636
10998	Notch1	notch 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991352
10998	Notch1	notch 1	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17336907
10998	Notch1	notch 1	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
10998	Notch1	notch 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
10998	Notch1	notch 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
10998	Notch1	notch 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:28395734
10998	Notch1	notch 1	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
10998	Notch1	notch 1	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20240530	MGI			PMID:28395734
10998	Notch1	notch 1	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10879540
10998	Notch1	notch 1	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23806616
10998	Notch1	notch 1	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
10998	Notch1	notch 1	gene	MP:0003794	delayed somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
10998	Notch1	notch 1	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
10998	Notch1	notch 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10879540
10998	Notch1	notch 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595837
10998	Notch1	notch 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16885355
10998	Notch1	notch 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926761
10998	Notch1	notch 1	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21311046
10998	Notch1	notch 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0004125	abnormal venule morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
10998	Notch1	notch 1	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
10998	Notch1	notch 1	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730124
10998	Notch1	notch 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163386
10998	Notch1	notch 1	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163386
10998	Notch1	notch 1	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080428
10998	Notch1	notch 1	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:37369584
10998	Notch1	notch 1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141228
10998	Notch1	notch 1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20240229	MGI			PMID:37369584
10998	Notch1	notch 1	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837254
10998	Notch1	notch 1	gene	MP:0004497	decreased organ of Corti supporting cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141228
10998	Notch1	notch 1	gene	MP:0004712	notochord degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19110448
10998	Notch1	notch 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658279
10998	Notch1	notch 1	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19110448
10998	Notch1	notch 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19110448
10998	Notch1	notch 1	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10879540
10998	Notch1	notch 1	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0005222	abnormal somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0005224	abnormal left-right axis symmetry of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21311046
10998	Notch1	notch 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17336907
10998	Notch1	notch 1	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0005544	cornea deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
10998	Notch1	notch 1	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0006093	arteriovenous malformation		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
10998	Notch1	notch 1	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21311046
10998	Notch1	notch 1	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
10998	Notch1	notch 1	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19110448
10998	Notch1	notch 1	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19110448
10998	Notch1	notch 1	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
10998	Notch1	notch 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
10998	Notch1	notch 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658279
10998	Notch1	notch 1	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19110448
10998	Notch1	notch 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991352
10998	Notch1	notch 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
10998	Notch1	notch 1	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095891
10998	Notch1	notch 1	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
10998	Notch1	notch 1	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15081359
10998	Notch1	notch 1	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0008987	abnormal liver lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0009004	progressive hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0009145	abnormal pancreatic acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
10998	Notch1	notch 1	gene	MP:0009165	abnormal endocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
10998	Notch1	notch 1	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
10998	Notch1	notch 1	gene	MP:0009328	delayed heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20935640
10998	Notch1	notch 1	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
10998	Notch1	notch 1	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
10998	Notch1	notch 1	gene	MP:0010500	myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21311046
10998	Notch1	notch 1	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21311046
10998	Notch1	notch 1	gene	MP:0010561	absent coronary vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:21311046
10998	Notch1	notch 1	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20181122	MGI			PMID:21493891
10998	Notch1	notch 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163386
10998	Notch1	notch 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23806616
10998	Notch1	notch 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22156581
10998	Notch1	notch 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10879540
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10367900
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16885355
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215306
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17229764
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227520
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789282
10998	Notch1	notch 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926761
10998	Notch1	notch 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
10998	Notch1	notch 1	gene	MP:0011181	increased hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
10998	Notch1	notch 1	gene	MP:0011934	abnormal branching involved in pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
10998	Notch1	notch 1	gene	MP:0011935	abnormal pancreatic bud formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
10998	Notch1	notch 1	gene	MP:0012246	abnormal hepatic cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
10998	Notch1	notch 1	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0012509	neural tube degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809373
10998	Notch1	notch 1	gene	MP:0012725	small sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
10998	Notch1	notch 1	gene	MP:0013464	decreased conjunctiva goblet cell number		IAGP		N	RGD:5509061	20150205	MGI			PMID:23293291
10998	Notch1	notch 1	gene	MP:0013925	abnormal vascular plexus formation		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
10998	Notch1	notch 1	gene	MP:0014148	lacrimal gland degeneration		IAGP		N	RGD:5509061	20160407	MGI			PMID:23293291
10998	Notch1	notch 1	gene	MP:0014154	Meibomian gland degeneration		IAGP		N	RGD:5509061	20160407	MGI			PMID:23293291
10998	Notch1	notch 1	gene	MP:0031124	aortic valve inflammation		IAGP		N	RGD:5509061	20200917	MGI			PMID:21493891
10998	Notch1	notch 1	gene	MP:0031301	chronic liver inflammation		IAGP		N	RGD:5509061	20211028	MGI			PMID:21266774
10998	Notch1	notch 1	gene	MP:0031518	calcified aortic valve cusp		IAGP		N	RGD:5509061	20240118	MGI			PMID:21493891
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9122228
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9122228
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9122228
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0002494	increased IgM level		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1781357
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9122228
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9122228
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0005093	decreased B cell proliferation		IEA		N	RGD:5509061	20141003	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9122228
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0008182	decreased marginal zone B cell number		IEA		N	RGD:5509061	20141003	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0010186	increased T follicular helper cell number		IEA		N	RGD:5509061	20141003	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1781356
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1781356
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0011476	abnormal urine nucleotide level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2516826
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0011477	abnormal urine nucleoside level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0011597	decreased purine-nucleoside phosphorylase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0011597	decreased purine-nucleoside phosphorylase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:1781357
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0011597	decreased purine-nucleoside phosphorylase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:2516826
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:10859343
10999	Pnp	purine-nucleoside phosphorylase	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20181011	MGI			
11000	Npm1	nucleophosmin 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20171109	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20171109	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11000	Npm1	nucleophosmin 1	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20171109	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11000	Npm1	nucleophosmin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11000	Npm1	nucleophosmin 1	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11000	Npm1	nucleophosmin 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11000	Npm1	nucleophosmin 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20171109	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0004049	increased acute promyelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21979879
11000	Npm1	nucleophosmin 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30692594
11000	Npm1	nucleophosmin 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11000	Npm1	nucleophosmin 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20171109	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20190418	MGI			PMID:30692594
11000	Npm1	nucleophosmin 1	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21979879
11000	Npm1	nucleophosmin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11000	Npm1	nucleophosmin 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21979879
11000	Npm1	nucleophosmin 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226219
11000	Npm1	nucleophosmin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11000	Npm1	nucleophosmin 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20171109	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11000	Npm1	nucleophosmin 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0011877	absent liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
11000	Npm1	nucleophosmin 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16199867
11000	Npm1	nucleophosmin 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16007073
11000	Npm1	nucleophosmin 1	gene	MP:0013660	abnormal bone marrow hematopoietic cell morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:30692594
11000	Npm1	nucleophosmin 1	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30692594
11003	Nppa	natriuretic peptide type A	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20180719	MGI			PMID:7839143
11003	Nppa	natriuretic peptide type A	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20180719	MGI			PMID:10848509
11003	Nppa	natriuretic peptide type A	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20180719	MGI			PMID:7839143
11003	Nppa	natriuretic peptide type A	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20180719	MGI			PMID:7839143
11003	Nppa	natriuretic peptide type A	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330043
11003	Nppa	natriuretic peptide type A	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20180719	MGI			PMID:10956626
11003	Nppa	natriuretic peptide type A	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10100923
11003	Nppa	natriuretic peptide type A	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330043
11003	Nppa	natriuretic peptide type A	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20180719	MGI			PMID:10484477
11003	Nppa	natriuretic peptide type A	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:7839143
11003	Nppa	natriuretic peptide type A	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20180719	MGI			PMID:10100923
11003	Nppa	natriuretic peptide type A	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330043
11003	Nppa	natriuretic peptide type A	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20180719	MGI			PMID:10484477
11003	Nppa	natriuretic peptide type A	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20180719	MGI			PMID:7839143
11003	Nppa	natriuretic peptide type A	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20180719	MGI			PMID:9458926
11003	Nppa	natriuretic peptide type A	gene	MP:0005532	abnormal vascular resistance		IAGP		N	RGD:5509061	20180719	MGI			PMID:10100923
11003	Nppa	natriuretic peptide type A	gene	MP:0005581	abnormal renin activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:9458926
11003	Nppa	natriuretic peptide type A	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330043
11003	Nppa	natriuretic peptide type A	gene	MP:0005662	increased circulating adrenaline level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10484477
11003	Nppa	natriuretic peptide type A	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20180719	MGI			PMID:10100923
11003	Nppa	natriuretic peptide type A	gene	MP:0008776	increased right ventricle peak pressure		IAGP		N	RGD:5509061	20180719	MGI			PMID:10330043
11003	Nppa	natriuretic peptide type A	gene	MP:0008776	increased right ventricle peak pressure		IAGP		N	RGD:5509061	20180719	MGI			PMID:10956626
11003	Nppa	natriuretic peptide type A	gene	MP:0010109	abnormal renal sodium reabsorption		IAGP		N	RGD:5509061	20180719	MGI			PMID:9458926
11003	Nppa	natriuretic peptide type A	gene	MP:0010755	abnormal heart right ventricle pressure		IAGP		N	RGD:5509061	20180719	MGI			PMID:10956626
11004	Nppb	natriuretic peptide type B	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10737768
11004	Nppb	natriuretic peptide type B	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10737768
11004	Nppb	natriuretic peptide type B	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10737768
11004	Nppb	natriuretic peptide type B	gene	MP:0014731	disorganized myocardial fiber myofibrils		IAGP		N	RGD:5509061	20250904	MGI			PMID:10737768
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997476
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9287305
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124219
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124219
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160929	MGI			PMID:25775533
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727932
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997476
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9287305
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124219
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727932
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769452
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23464624
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20160929	MGI			PMID:25775533
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769452
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477288
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002295	abnormal pulmonary circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23464624
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537139
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537139
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23464624
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477288
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482923
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20160929	MGI			PMID:25775533
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482923
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457873
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0003353	decreased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0004044	aortic dissection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727932
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0004216	salt-resistant hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477288
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0004216	salt-resistant hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23464624
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0005522	increased circulating atrial natriuretic factor		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124219
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0005522	increased circulating atrial natriuretic factor		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727932
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0005522	increased circulating atrial natriuretic factor		IAGP		N	RGD:5509061	20141003	MGI			PMID:9287305
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727932
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0005647	abnormal sex gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10537139
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727932
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769452
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405681
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477288
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23464624
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477288
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727932
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457873
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20160929	MGI			PMID:25775533
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0015067	increased myocardial fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:12727932
11007	Npr1	natriuretic peptide receptor 1	gene	MP:0031080	pulmonary embolism		IAGP		N	RGD:5509061	20200709	MGI			PMID:9405681
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20111116	MGI			
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002758	long tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004641	elongated metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004651	increased thoracic vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004685	calcified intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004695	increased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004695	increased length of long bones		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004703	abnormal vertebral column morphology		IEA		N	RGD:5509061	20111116	MGI			
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004705	elongated vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004705	elongated vertebral body		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0005229	abnormal intervertebral disk development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0006253	clinodactyly		IEA		N	RGD:5509061	20111116	MGI			
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0006296	arachnodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0006296	arachnodactyly		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0006320	abnormal interscapular fat pad morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:22307324
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0006392	abnormal nucleus pulposus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0006393	absent nucleus pulposus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0006394	abnormal vertebral epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10468599
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0006394	abnormal vertebral epiphyseal plate morphology		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0008771	elongated vertebral column		IEA		N	RGD:5509061	20111116	MGI			
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0008833	caudal hemivertebra		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20180111	MGI			PMID:22307324
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20180111	MGI			PMID:22307324
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:22307324
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:22307324
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:22307324
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:22307324
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20190110	MGI			PMID:27959934
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0010128	hypovolemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0011476	abnormal urine nucleotide level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377427
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20141003	MGI			
11008	Npr3	natriuretic peptide receptor 3	gene	MP:0013138	thin body		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
11016	Npy	neuropeptide Y	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632796
11016	Npy	neuropeptide Y	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339312
11016	Npy	neuropeptide Y	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18616565
11016	Npy	neuropeptide Y	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18616565
11016	Npy	neuropeptide Y	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18616565
11016	Npy	neuropeptide Y	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
11016	Npy	neuropeptide Y	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077332
11016	Npy	neuropeptide Y	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160310	MGI			PMID:26402609
11016	Npy	neuropeptide Y	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18616565
11016	Npy	neuropeptide Y	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339312
11016	Npy	neuropeptide Y	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632796
11016	Npy	neuropeptide Y	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
11016	Npy	neuropeptide Y	gene	MP:0003867	increased defecation amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18616565
11016	Npy	neuropeptide Y	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
11016	Npy	neuropeptide Y	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
11016	Npy	neuropeptide Y	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
11016	Npy	neuropeptide Y	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339312
11016	Npy	neuropeptide Y	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
11016	Npy	neuropeptide Y	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
11016	Npy	neuropeptide Y	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:20613867
11016	Npy	neuropeptide Y	gene	MP:0014145	increased white adipose tissue mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:20613867
11016	Npy	neuropeptide Y	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:20613867
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9623983
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:10698177
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:14525913
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:9623983
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9623983
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20230119	MGI			
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14525913
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14525913
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9623983
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230119	MGI			
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230119	MGI			
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16636293
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14525913
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9623983
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14525913
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9623983
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:10698177
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11017	Npy5r	neuropeptide Y receptor Y5	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20151119	MGI			PMID:22768253
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23733505
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23733505
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23733505
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180719	MGI			PMID:21586752
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180719	MGI			PMID:23733505
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:25252692
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20180719	MGI			PMID:25252692
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180719	MGI			PMID:23733505
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:21586752
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20179099
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:23733505
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:23733505
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:11238881
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:18059342
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:23418499
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:7878045
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002738	hyperresponsive to tactile stimuli		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20220811	MGI			
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20180719	MGI			PMID:18372904
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0009391	abnormal leptomeninges pigmentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010273	increased classified tumor incidence		IAGP		N	RGD:5509061	20260409	MGI			PMID:37756546
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010322	increased cutaneous melanoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:25252692
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010336	increased acute lymphoblastic leukemia incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:23733505
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:23733505
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010741	abnormal melanocyte proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23303902
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0010741	abnormal melanocyte proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:25252692
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:18059342
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:18059342
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:21586752
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:22876308
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:18059342
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0011995	decreased leukemia incidence		IAGP		N	RGD:5509061	20211021	MGI			PMID:26493479
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20180719	MGI			PMID:20179099
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0014518	myocardial hypertrabeculation		IAGP		N	RGD:5509061	20240822	MGI			PMID:33681212
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0014660	increased skin nevi incidence		IAGP		N	RGD:5509061	20250508	MGI			PMID:25252692
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:9334313
11018	Nras	Nras proto-oncogene, GTPase	gene	MP:0031555	abnormal pulmonary valve development		IAGP		N	RGD:5509061	20240125	MGI			PMID:33681212
11020	Nrdc	nardilysin convertase	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11020	Nrdc	nardilysin convertase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19935654
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337809
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337809
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337809
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001054	failure of neuromuscular synapse presynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001055	failure of neuromuscular synapse postsynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337809
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337809
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337809
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18718936
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337809
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8653786
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337809
11021	Musk	muscle, skeletal, receptor tyrosine kinase	gene	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm		IAGP		N	RGD:5509061	20170720	MGI			PMID:25810523
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925599
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20181227	MGI			
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23776632
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10798407
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19158294
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728915
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10798407
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000910	small facial motor nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402890
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10571233
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402890
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000959	abnormal somatic sensory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000959	abnormal somatic sensory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728915
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402890
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009525
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000972	abnormal mechanoreceptor morphology		IAGP		N	RGD:5509061	20231026	MGI			PMID:30126905
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0000980	absent hair-down neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728915
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001021	small L4 dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001072	abnormal vestibulocochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001085	small petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728915
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402890
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013804
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:23776632
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19158294
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11681842
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23776632
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23776632
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11681842
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:19158294
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728915
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832146
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:23774276
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001411	spinning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725924
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001435	absent suckling reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402890
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001437	no swallowing reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402890
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001462	abnormal avoidance learning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10571233
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10571233
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10571233
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10571233
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832146
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001490	abnormal vibrissae reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402890
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001500	decreased kindling response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15233915
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23776632
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367511
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10571233
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10571233
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15820690
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21192928
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21192928
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367511
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21192928
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002638	abnormal pupillary reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232675
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232675
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013804
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10571233
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832146
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19158294
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10798407
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367511
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21192928
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925599
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013804
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:23776632
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003986	small cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003986	small cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728915
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009525
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004220	abnormal peripheral nervous system regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745667
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004409	abnormal crista ampullaris neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004427	abnormal vestibular labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004428	abnormal type I vestibular cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925599
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004716	abnormal cochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004718	abnormal vestibular nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004718	abnormal vestibular nerve morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004747	abnormal cochlear OHC afferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925599
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0004747	abnormal cochlear OHC afferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0005345	abnormal circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232675
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0005345	abnormal circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11681842
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23776632
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11681842
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17611278
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10798407
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17611278
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832146
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19158294
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008299	adrenal cortical hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728915
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23774276
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10798407
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20160421	MGI			
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009286	increased abdominal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23776632
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:23774276
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832146
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20150312	MGI			PMID:25525881
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10516311
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11681842
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654337
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372074
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23776632
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22196735
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402890
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21192928
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21192928
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0014286	increased adrenal gland zona fasciculata size		IAGP		N	RGD:5509061	20230907	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20240405	MGI			PMID:12925599
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0014490	abnormal inner ear vestibular sensory neuron innervation pattern		IAGP		N	RGD:5509061	20240801	MGI			PMID:11877382
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0014490	abnormal inner ear vestibular sensory neuron innervation pattern		IAGP		N	RGD:5509061	20240801	MGI			PMID:12925599
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0014490	abnormal inner ear vestibular sensory neuron innervation pattern		IAGP		N	RGD:5509061	20240801	MGI			PMID:7588071
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0014491	abnormal mammary gland sensory innervation pattern		IAGP		N	RGD:5509061	20240801	MGI			PMID:23224557
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:24619096
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0031018	decreased granulosa cell proliferation		IAGP		N	RGD:5509061	20200130	MGI			PMID:15013804
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:15013804
11023	Ntrk2	neurotrophic tyrosine kinase, receptor, type 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:23774276
11024	Nxph1	neurexophilin 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856994
11024	Nxph1	neurexophilin 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856994
11027	Oca2	oculocutaneous albinism II	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8389469
11027	Oca2	oculocutaneous albinism II	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0000184	abnormal circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12644183
11027	Oca2	oculocutaneous albinism II	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:13943454
11027	Oca2	oculocutaneous albinism II	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:1495987
11027	Oca2	oculocutaneous albinism II	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:1509264
11027	Oca2	oculocutaneous albinism II	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575552
11027	Oca2	oculocutaneous albinism II	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0000421	mottled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673574
11027	Oca2	oculocutaneous albinism II	gene	MP:0000421	mottled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:5094803
11027	Oca2	oculocutaneous albinism II	gene	MP:0000423	delayed hair regrowth		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0000427	abnormal hair cycle		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0001124	abnormal gametes		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689098
11027	Oca2	oculocutaneous albinism II	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14402638
11027	Oca2	oculocutaneous albinism II	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20260402	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:13943454
11027	Oca2	oculocutaneous albinism II	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673574
11027	Oca2	oculocutaneous albinism II	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575552
11027	Oca2	oculocutaneous albinism II	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689098
11027	Oca2	oculocutaneous albinism II	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:14402638
11027	Oca2	oculocutaneous albinism II	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689098
11027	Oca2	oculocutaneous albinism II	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14402638
11027	Oca2	oculocutaneous albinism II	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1495987
11027	Oca2	oculocutaneous albinism II	gene	MP:0001922	reduced male fertility		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14402638
11027	Oca2	oculocutaneous albinism II	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7317942
11027	Oca2	oculocutaneous albinism II	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689098
11027	Oca2	oculocutaneous albinism II	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14402638
11027	Oca2	oculocutaneous albinism II	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7317942
11027	Oca2	oculocutaneous albinism II	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8389469
11027	Oca2	oculocutaneous albinism II	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1495987
11027	Oca2	oculocutaneous albinism II	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247308
11027	Oca2	oculocutaneous albinism II	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575552
11027	Oca2	oculocutaneous albinism II	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12644183
11027	Oca2	oculocutaneous albinism II	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:1495987
11027	Oca2	oculocutaneous albinism II	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14402638
11027	Oca2	oculocutaneous albinism II	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7317942
11027	Oca2	oculocutaneous albinism II	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0002089	abnormal postnatal growth/weight/body size		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0002161	abnormal fertility/fecundity		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20120126	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0002412	increased susceptibility to bacterial infection		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074018
11027	Oca2	oculocutaneous albinism II	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575552
11027	Oca2	oculocutaneous albinism II	gene	MP:0003171	phenotypic reversion		IAGP		N	RGD:5509061	20141003	MGI			PMID:1495987
11027	Oca2	oculocutaneous albinism II	gene	MP:0003171	phenotypic reversion		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673574
11027	Oca2	oculocutaneous albinism II	gene	MP:0003171	phenotypic reversion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8419934
11027	Oca2	oculocutaneous albinism II	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074018
11027	Oca2	oculocutaneous albinism II	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IEA		N	RGD:5509061	20141003	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074018
11027	Oca2	oculocutaneous albinism II	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0005072	abnormal hair follicle melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247308
11027	Oca2	oculocutaneous albinism II	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11027	Oca2	oculocutaneous albinism II	gene	MP:0005077	abnormal melanogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11027	Oca2	oculocutaneous albinism II	gene	MP:0005114	premature hair loss		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14402638
11027	Oca2	oculocutaneous albinism II	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1495987
11027	Oca2	oculocutaneous albinism II	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1509264
11027	Oca2	oculocutaneous albinism II	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673574
11027	Oca2	oculocutaneous albinism II	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0005366	variegated coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673574
11027	Oca2	oculocutaneous albinism II	gene	MP:0005409	darkened coat color		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:1495987
11027	Oca2	oculocutaneous albinism II	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14402638
11027	Oca2	oculocutaneous albinism II	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7317942
11027	Oca2	oculocutaneous albinism II	gene	MP:0006159	ocular albinism		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0008480	absent eye pigmentation		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20180927	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074018
11027	Oca2	oculocutaneous albinism II	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0008912	nervous		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0009233	enlarged sperm head		IAGP		N	RGD:5509061	20141003	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0009554	abnormal hair follicle melanin granule shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247308
11027	Oca2	oculocutaneous albinism II	gene	MP:0009555	abnormal hair follicle melanin granule distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247308
11027	Oca2	oculocutaneous albinism II	gene	MP:0010193	abnormal choroid melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11027	Oca2	oculocutaneous albinism II	gene	MP:0010389	mosaic coat color		IEA		N	RGD:5509061	20150507	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0010766	abnormal NK cell physiology		IEA		N	RGD:5509061	20111116	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7317942
11027	Oca2	oculocutaneous albinism II	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1495987
11027	Oca2	oculocutaneous albinism II	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074018
11027	Oca2	oculocutaneous albinism II	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051828
11027	Oca2	oculocutaneous albinism II	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8601493
11027	Oca2	oculocutaneous albinism II	gene	MP:0011277	decreased tail pigmentation		IEA		N	RGD:5509061	20120126	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0011279	decreased ear pigmentation		IEA		N	RGD:5509061	20141003	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0011400	lethality, complete penetrance		IEA		N	RGD:5509061	20120126	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0011627	decreased skin pigmentation		IEA		N	RGD:5509061	20141003	MGI			
11027	Oca2	oculocutaneous albinism II	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:5565073
11027	Oca2	oculocutaneous albinism II	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:9689098
11028	Ocm	oncomodulin	gene	MP:0001967	deafness		IEA		N	RGD:5509061	20111116	MGI			
11028	Ocm	oncomodulin	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20190613	MGI			PMID:26843644
11028	Ocm	oncomodulin	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20190613	MGI			PMID:26843644
11028	Ocm	oncomodulin	gene	MP:0004586	pillar cell degeneration		IAGP		N	RGD:5509061	20190613	MGI			PMID:26843644
11028	Ocm	oncomodulin	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20190613	MGI			PMID:26843644
11028	Ocm	oncomodulin	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20190613	MGI			PMID:26843644
11028	Ocm	oncomodulin	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20170105	MGI			
11028	Ocm	oncomodulin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20190613	MGI			PMID:26843644
11028	Ocm	oncomodulin	gene	MP:0011968	decreased threshold for auditory brainstem response		IAGP		N	RGD:5509061	20190613	MGI			PMID:26843644
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22037768
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22037768
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22037768
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22037768
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22037768
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22037768
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22037768
11032	Odf1	outer dense fiber of sperm tails 1	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22037768
11034	Omp	olfactory marker protein	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15157418
11034	Omp	olfactory marker protein	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537788
11034	Omp	olfactory marker protein	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21613506
11034	Omp	olfactory marker protein	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
11034	Omp	olfactory marker protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22057188
11034	Omp	olfactory marker protein	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20210805	MGI			PMID:34186026
11034	Omp	olfactory marker protein	gene	MP:0001983	abnormal olfactory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22057188
11034	Omp	olfactory marker protein	gene	MP:0001983	abnormal olfactory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
11034	Omp	olfactory marker protein	gene	MP:0001983	abnormal olfactory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790421
11034	Omp	olfactory marker protein	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:21613506
11034	Omp	olfactory marker protein	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20160623	MGI			PMID:26046438
11034	Omp	olfactory marker protein	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
11034	Omp	olfactory marker protein	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20161229	MGI			PMID:21957232
11034	Omp	olfactory marker protein	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790421
11034	Omp	olfactory marker protein	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
11034	Omp	olfactory marker protein	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0003462	abnormal response to novel odor		IAGP		N	RGD:5509061	20210805	MGI			PMID:34186026
11034	Omp	olfactory marker protein	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20191226	MGI			PMID:31653840
11034	Omp	olfactory marker protein	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15157418
11034	Omp	olfactory marker protein	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17493809
11034	Omp	olfactory marker protein	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537788
11034	Omp	olfactory marker protein	gene	MP:0005499	abnormal olfactory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
11034	Omp	olfactory marker protein	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790421
11034	Omp	olfactory marker protein	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17521568
11034	Omp	olfactory marker protein	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035080
11034	Omp	olfactory marker protein	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
11034	Omp	olfactory marker protein	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22057188
11034	Omp	olfactory marker protein	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
11034	Omp	olfactory marker protein	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
11034	Omp	olfactory marker protein	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20171116	MGI			PMID:28495971
11034	Omp	olfactory marker protein	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
11034	Omp	olfactory marker protein	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
11034	Omp	olfactory marker protein	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035080
11034	Omp	olfactory marker protein	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:21957232
11034	Omp	olfactory marker protein	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
11034	Omp	olfactory marker protein	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
11034	Omp	olfactory marker protein	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28815295
11034	Omp	olfactory marker protein	gene	MP:0010055	abnormal sensory neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22057188
11034	Omp	olfactory marker protein	gene	MP:0010057	abnormal olfactory bulb outer nerve layer morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
11034	Omp	olfactory marker protein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0011677	abnormal olfactory sensory neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
11034	Omp	olfactory marker protein	gene	MP:0011677	abnormal olfactory sensory neuron physiology		IAGP		N	RGD:5509061	20161229	MGI			PMID:21957232
11034	Omp	olfactory marker protein	gene	MP:0011677	abnormal olfactory sensory neuron physiology		IAGP		N	RGD:5509061	20171116	MGI			PMID:28495971
11034	Omp	olfactory marker protein	gene	MP:0011677	abnormal olfactory sensory neuron physiology		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0011678	abnormal vomeronasal sensory neuron physiology		IAGP		N	RGD:5509061	20191226	MGI			PMID:31653840
11034	Omp	olfactory marker protein	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035080
11034	Omp	olfactory marker protein	gene	MP:0012020	abnormal olfactory epithelium physiology		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0020348	decreased olfactory sensory neuron number		IAGP		N	RGD:5509061	20161229	MGI			PMID:21957232
11034	Omp	olfactory marker protein	gene	MP:0020348	decreased olfactory sensory neuron number		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
11034	Omp	olfactory marker protein	gene	MP:0020348	decreased olfactory sensory neuron number		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
11034	Omp	olfactory marker protein	gene	MP:0020852	abnormal olfactory behavior		IAGP		N	RGD:5509061	20240229	MGI			PMID:36330924
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647741
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647741
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647741
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647741
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16840715
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20241121	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20241121	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20210520	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446599
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201022	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20201231	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210520	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647741
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20241121	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210520	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647741
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20201022	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446599
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0004290	abnormal stapes footplate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0004290	abnormal stapes footplate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0004897	otosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446599
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446599
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16840715
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0006133	calcified artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0008233	abnormal pro-B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160187
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647741
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0009084	blind uterus		IEA		N	RGD:5509061	20210826	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20241121	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0010663	abnormal brachiocephalic trunk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16840715
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0010870	absent bone trabeculae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9647741
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20240405	MGI			PMID:16467704
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0030281	thin parietal bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:9573043
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0030399	abnormal incus body morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0030400	abnormal stapes annular ligament morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:16564235
11035	Tnfrsf11b	tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin)	gene	MP:0030793	short femur neck		IAGP		N	RGD:5509061	20181018	MGI			PMID:11160187
11036	Oprd1	opioid receptor, delta 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835636
11036	Oprd1	opioid receptor, delta 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835636
11036	Oprd1	opioid receptor, delta 1	gene	MP:0001980	abnormal chemically-elicited antinociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486185
11036	Oprd1	opioid receptor, delta 1	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21295407
11036	Oprd1	opioid receptor, delta 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IEA		N	RGD:5509061	20111116	MGI			
11036	Oprd1	opioid receptor, delta 1	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835636
11036	Oprd1	opioid receptor, delta 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17544222
11036	Oprd1	opioid receptor, delta 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21295407
11036	Oprd1	opioid receptor, delta 1	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486185
11036	Oprd1	opioid receptor, delta 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20141003	MGI			PMID:17544222
11036	Oprd1	opioid receptor, delta 1	gene	MP:0009778	impaired behavioral response to anesthetic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17544222
11038694	Pas19_m	pulmonary adenoma susceptibility 19 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160219	MGI		Created by mouse qtl pipeline	PMID:12810665
11038694	Pas19_m	pulmonary adenoma susceptibility 19 (mouse)	qtl	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:7813906
11038694	Pas19_m	pulmonary adenoma susceptibility 19 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12810665
11038830	Trdn	triadin	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:19843516
11038830	Trdn	triadin	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20160304	MGI			PMID:19843516
11038830	Trdn	triadin	gene	MP:0009411	abnormal skeletal muscle fiber triad morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:17981799
11038830	Trdn	triadin	gene	MP:0009411	abnormal skeletal muscle fiber triad morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:19843516
11038830	Trdn	triadin	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20160304	MGI			PMID:19843516
11038830	Trdn	triadin	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160304	MGI			PMID:19843516
11038830	Trdn	triadin	gene	MP:0014915	decreased muscle cell calcium uptake		IAGP		N	RGD:5509061	20260219	MGI			PMID:19843516
11038830	Trdn	triadin	gene	MP:0014918	decreased muscle cell calcium release		IAGP		N	RGD:5509061	20260219	MGI			PMID:19843516
11039	Otc	ornithine transcarbamylase	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0000414	alopecia		IEA		N	RGD:5509061	20111116	MGI			
11039	Otc	ornithine transcarbamylase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180719	MGI			PMID:25647322
11039	Otc	ornithine transcarbamylase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180719	MGI			PMID:3162766
11039	Otc	ornithine transcarbamylase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180719	MGI			PMID:4603259
11039	Otc	ornithine transcarbamylase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180719	MGI			PMID:5727
11039	Otc	ornithine transcarbamylase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180719	MGI			PMID:8461026
11039	Otc	ornithine transcarbamylase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0000418	focal hair loss		IEA		N	RGD:5509061	20111116	MGI			
11039	Otc	ornithine transcarbamylase	gene	MP:0000422	delayed hair appearance		IEA		N	RGD:5509061	20111116	MGI			
11039	Otc	ornithine transcarbamylase	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20180719	MGI			PMID:1531355
11039	Otc	ornithine transcarbamylase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8108192
11039	Otc	ornithine transcarbamylase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20180719	MGI			PMID:2920015
11039	Otc	ornithine transcarbamylase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
11039	Otc	ornithine transcarbamylase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20180719	MGI			PMID:9630607
11039	Otc	ornithine transcarbamylase	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8108192
11039	Otc	ornithine transcarbamylase	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:3162766
11039	Otc	ornithine transcarbamylase	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:5727
11039	Otc	ornithine transcarbamylase	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:16497529
11039	Otc	ornithine transcarbamylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:25647322
11039	Otc	ornithine transcarbamylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:5727
11039	Otc	ornithine transcarbamylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20180719	MGI			PMID:16497529
11039	Otc	ornithine transcarbamylase	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20111116	MGI			
11039	Otc	ornithine transcarbamylase	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20220519	MGI			
11039	Otc	ornithine transcarbamylase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20180719	MGI			PMID:7827141
11039	Otc	ornithine transcarbamylase	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20180719	MGI			PMID:1531355
11039	Otc	ornithine transcarbamylase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20180719	MGI			PMID:4603259
11039	Otc	ornithine transcarbamylase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:25647322
11039	Otc	ornithine transcarbamylase	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20180719	MGI			PMID:5727
11039	Otc	ornithine transcarbamylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:8461026
11039	Otc	ornithine transcarbamylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8108192
11039	Otc	ornithine transcarbamylase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:1531355
11039	Otc	ornithine transcarbamylase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:7816342
11039	Otc	ornithine transcarbamylase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8041507
11039	Otc	ornithine transcarbamylase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8108192
11039	Otc	ornithine transcarbamylase	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220519	MGI			
11039	Otc	ornithine transcarbamylase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:2920015
11039	Otc	ornithine transcarbamylase	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0003415	priapism		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20180719	MGI			PMID:1627360
11039	Otc	ornithine transcarbamylase	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:7827141
11039	Otc	ornithine transcarbamylase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20180719	MGI			PMID:1575747
11039	Otc	ornithine transcarbamylase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20180719	MGI			PMID:8424807
11039	Otc	ornithine transcarbamylase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20180719	MGI			PMID:1575747
11039	Otc	ornithine transcarbamylase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20180719	MGI			PMID:16497529
11039	Otc	ornithine transcarbamylase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20180719	MGI			PMID:3162766
11039	Otc	ornithine transcarbamylase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7816342
11039	Otc	ornithine transcarbamylase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8424807
11039	Otc	ornithine transcarbamylase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20180719	MGI			PMID:25647322
11039	Otc	ornithine transcarbamylase	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7828023
11039	Otc	ornithine transcarbamylase	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20180719	MGI			PMID:1575747
11039	Otc	ornithine transcarbamylase	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20180719	MGI			PMID:25647322
11039	Otc	ornithine transcarbamylase	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7828023
11039	Otc	ornithine transcarbamylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:2920015
11039	Otc	ornithine transcarbamylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:8424807
11039	Otc	ornithine transcarbamylase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:2920015
11039	Otc	ornithine transcarbamylase	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9630607
11039	Otc	ornithine transcarbamylase	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20180719	MGI			PMID:16497529
11039	Otc	ornithine transcarbamylase	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20180719	MGI			PMID:16497529
11039	Otc	ornithine transcarbamylase	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20180719	MGI			PMID:2920015
11039	Otc	ornithine transcarbamylase	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180719	MGI			PMID:16497529
11039	Otc	ornithine transcarbamylase	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20180719	MGI			PMID:25647322
11039	Otc	ornithine transcarbamylase	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:7827141
11039	Otc	ornithine transcarbamylase	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9630607
11039	Otc	ornithine transcarbamylase	gene	MP:0010028	aciduria		IAGP		N	RGD:5509061	20180719	MGI			PMID:8461026
11039	Otc	ornithine transcarbamylase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:7930593
11039	Otc	ornithine transcarbamylase	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20180719	MGI			PMID:9630607
11039	Otc	ornithine transcarbamylase	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20180719	MGI			
11039	Otc	ornithine transcarbamylase	gene	MP:0011588	decreased ornithine carbamoyltransferase activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:3981356
11039	Otc	ornithine transcarbamylase	gene	MP:0011588	decreased ornithine carbamoyltransferase activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:5727
11039	Otc	ornithine transcarbamylase	gene	MP:0011588	decreased ornithine carbamoyltransferase activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:6623083
11039	Otc	ornithine transcarbamylase	gene	MP:0011588	decreased ornithine carbamoyltransferase activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0011588	decreased ornithine carbamoyltransferase activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:7816342
11039	Otc	ornithine transcarbamylase	gene	MP:0011588	decreased ornithine carbamoyltransferase activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:7828023
11039	Otc	ornithine transcarbamylase	gene	MP:0011626	orotic acid urinary bladder stones		IAGP		N	RGD:5509061	20180719	MGI			PMID:5727
11039	Otc	ornithine transcarbamylase	gene	MP:0011765	oroticaciduria		IAGP		N	RGD:5509061	20180719	MGI			PMID:3162766
11039	Otc	ornithine transcarbamylase	gene	MP:0011765	oroticaciduria		IAGP		N	RGD:5509061	20180719	MGI			PMID:7707692
11039	Otc	ornithine transcarbamylase	gene	MP:0011765	oroticaciduria		IAGP		N	RGD:5509061	20180719	MGI			PMID:7827141
11039	Otc	ornithine transcarbamylase	gene	MP:0011765	oroticaciduria		IAGP		N	RGD:5509061	20180719	MGI			PMID:8221965
11039	Otc	ornithine transcarbamylase	gene	MP:0011765	oroticaciduria		IAGP		N	RGD:5509061	20180719	MGI			PMID:8461026
11039	Otc	ornithine transcarbamylase	gene	MP:0011765	oroticaciduria		IAGP		N	RGD:5509061	20180920	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0012638	decreased brain monoamine oxidase activity		IAGP		N	RGD:5509061	20260709	MGI			PMID:8041507
11039	Otc	ornithine transcarbamylase	gene	MP:0012639	increased brain monoamine oxidase activity		IAGP		N	RGD:5509061	20260709	MGI			PMID:8041507
11039	Otc	ornithine transcarbamylase	gene	MP:0014956	decreased mitochondria enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:3162766
11039	Otc	ornithine transcarbamylase	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:7816342
11039	Otc	ornithine transcarbamylase	gene	MP:0014967	increased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:3162766
11039	Otc	ornithine transcarbamylase	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:3162766
11039	Otc	ornithine transcarbamylase	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:6623083
11039	Otc	ornithine transcarbamylase	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:7816342
11039	Otc	ornithine transcarbamylase	gene	MP:0020837	decreased circulating citrulline level		IAGP		N	RGD:5509061	20180913	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0030648	decreased ornithine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:7828023
11039	Otc	ornithine transcarbamylase	gene	MP:0030651	decreased circulating ornithine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0030662	decreased circulating arginine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:8750014
11039	Otc	ornithine transcarbamylase	gene	MP:0030706	increased glutamine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:1575747
11039	Otc	ornithine transcarbamylase	gene	MP:0030709	increased circulating glutamine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:1575747
11039	Otc	ornithine transcarbamylase	gene	MP:0030709	increased circulating glutamine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:8750014
11040	Oxt	oxytocin	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20150129	MGI			PMID:25157144
11040	Oxt	oxytocin	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:16249339
11040	Oxt	oxytocin	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888874
11040	Oxt	oxytocin	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12746288
11040	Oxt	oxytocin	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876199
11040	Oxt	oxytocin	gene	MP:0001422	abnormal drinking behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11573985
11040	Oxt	oxytocin	gene	MP:0001432	abnormal food preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:11573985
11040	Oxt	oxytocin	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9181490
11040	Oxt	oxytocin	gene	MP:0001460	abnormal olfactory discrimination memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888874
11040	Oxt	oxytocin	gene	MP:0001460	abnormal olfactory discrimination memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:11588199
11040	Oxt	oxytocin	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531722
11040	Oxt	oxytocin	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531722
11040	Oxt	oxytocin	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10026810
11040	Oxt	oxytocin	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8933362
11040	Oxt	oxytocin	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888874
11040	Oxt	oxytocin	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17895964
11040	Oxt	oxytocin	gene	MP:0003838	abnormal milk ejection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876199
11040	Oxt	oxytocin	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9181490
11040	Oxt	oxytocin	gene	MP:0004184	abnormal baroreceptor physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531722
11040	Oxt	oxytocin	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028821
11040	Oxt	oxytocin	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:10026810
11040	Oxt	oxytocin	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:9181490
11040	Oxt	oxytocin	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028821
11040	Oxt	oxytocin	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10026810
11040	Oxt	oxytocin	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17895964
11040	Oxt	oxytocin	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751758
11040	Oxt	oxytocin	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028821
11040	Oxt	oxytocin	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751758
11040	Oxt	oxytocin	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15718385
11040	Oxt	oxytocin	gene	MP:0012008	delayed parturition		IAGP		N	RGD:5509061	20191219	MGI			PMID:9751758
11040	Oxt	oxytocin	gene	MP:0013718	galactostasis		IAGP		N	RGD:5509061	20150409	MGI			PMID:10026810
11040	Oxt	oxytocin	gene	MP:0013718	galactostasis		IAGP		N	RGD:5509061	20150409	MGI			PMID:8933362
11040	Oxt	oxytocin	gene	MP:0014441	decreased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:23028821
11040	Oxt	oxytocin	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:11573985
11040	Oxt	oxytocin	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:17895964
11040464	Lncpnky	lncRNA Pou3f2 adjacent neural key regulator	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
11040464	Lncpnky	lncRNA Pou3f2 adjacent neural key regulator	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
11040464	Lncpnky	lncRNA Pou3f2 adjacent neural key regulator	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
11040464	Lncpnky	lncRNA Pou3f2 adjacent neural key regulator	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
11040464	Lncpnky	lncRNA Pou3f2 adjacent neural key regulator	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
11040464	Lncpnky	lncRNA Pou3f2 adjacent neural key regulator	gene	MP:0012204	abnormal neuronal stem cell physiology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
11041	Oxtr	oxytocin receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
11041	Oxtr	oxytocin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18356275
11041	Oxtr	oxytocin receptor	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:16249339
11041	Oxtr	oxytocin receptor	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16249339
11041	Oxtr	oxytocin receptor	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18356275
11041	Oxtr	oxytocin receptor	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872596
11041	Oxtr	oxytocin receptor	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:16249339
11041	Oxtr	oxytocin receptor	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16249339
11041	Oxtr	oxytocin receptor	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872596
11041	Oxtr	oxytocin receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18356275
11041	Oxtr	oxytocin receptor	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872596
11041	Oxtr	oxytocin receptor	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18356275
11041	Oxtr	oxytocin receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18356275
11041	Oxtr	oxytocin receptor	gene	MP:0003838	abnormal milk ejection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18356275
11041	Oxtr	oxytocin receptor	gene	MP:0009326	absent maternal crouching		IAGP		N	RGD:5509061	20141003	MGI			PMID:16249339
11041	Oxtr	oxytocin receptor	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16249339
11041	Oxtr	oxytocin receptor	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:16249339
11041	Oxtr	oxytocin receptor	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:16249339
11042	P2rx1	purinergic receptor P2X, ligand-gated ion channel, 1	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10638758
11042	P2rx1	purinergic receptor P2X, ligand-gated ion channel, 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10638758
11042	P2rx1	purinergic receptor P2X, ligand-gated ion channel, 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10638758
11042	P2rx1	purinergic receptor P2X, ligand-gated ion channel, 1	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10638758
11042	P2rx1	purinergic receptor P2X, ligand-gated ion channel, 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10638758
11043	P2ry1	purinergic receptor P2Y, G-protein coupled 1	gene	MP:0003422	abnormal thrombolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502826
11043	P2ry1	purinergic receptor P2Y, G-protein coupled 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502826
11043	P2ry1	purinergic receptor P2Y, G-protein coupled 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:10606627
11043	P2ry1	purinergic receptor P2Y, G-protein coupled 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502826
11043	P2ry1	purinergic receptor P2Y, G-protein coupled 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10606627
11043	P2ry1	purinergic receptor P2Y, G-protein coupled 1	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:10606627
11045	P2rx6	purinergic receptor P2X, ligand-gated ion channel, 6	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20141003	MGI			
11045	P2rx6	purinergic receptor P2X, ligand-gated ion channel, 6	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IEA		N	RGD:5509061	20141003	MGI			
11046	P4hb	prolyl 4-hydroxylase, beta polypeptide	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460613
11046	P4hb	prolyl 4-hydroxylase, beta polypeptide	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
11046	P4hb	prolyl 4-hydroxylase, beta polypeptide	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20191205	MGI			PMID:26529254
11046	P4hb	prolyl 4-hydroxylase, beta polypeptide	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460613
11046	P4hb	prolyl 4-hydroxylase, beta polypeptide	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20191205	MGI			PMID:26529254
11046	P4hb	prolyl 4-hydroxylase, beta polypeptide	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20191205	MGI			PMID:26529254
11046	P4hb	prolyl 4-hydroxylase, beta polypeptide	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11046	P4hb	prolyl 4-hydroxylase, beta polypeptide	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
11046	P4hb	prolyl 4-hydroxylase, beta polypeptide	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200924	MGI			PMID:26529254
11049307	Cdiptos	CDIP transferase, opposite strand	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240801	MGI			PMID:35122073
11050	Pah	phenylalanine hydroxylase	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
11050	Pah	phenylalanine hydroxylase	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11050	Pah	phenylalanine hydroxylase	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220519	MGI			
11050	Pah	phenylalanine hydroxylase	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640623
11050	Pah	phenylalanine hydroxylase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
11050	Pah	phenylalanine hydroxylase	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
11050	Pah	phenylalanine hydroxylase	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11050	Pah	phenylalanine hydroxylase	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0001460	abnormal olfactory discrimination memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:10407053
11050	Pah	phenylalanine hydroxylase	gene	MP:0001496	audiogenic seizures		IEA		N	RGD:5509061	20111116	MGI			
11050	Pah	phenylalanine hydroxylase	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230601	MGI			PMID:11487255
11050	Pah	phenylalanine hydroxylase	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
11050	Pah	phenylalanine hydroxylase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10767173
11050	Pah	phenylalanine hydroxylase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10407053
11050	Pah	phenylalanine hydroxylase	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
11050	Pah	phenylalanine hydroxylase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0002204	abnormal synaptic neurotransmitter level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20220519	MGI			
11050	Pah	phenylalanine hydroxylase	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10767173
11050	Pah	phenylalanine hydroxylase	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2308957
11050	Pah	phenylalanine hydroxylase	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11050	Pah	phenylalanine hydroxylase	gene	MP:0008732	reduced hair shaft melanin granule number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0009358	environmentally induced seizures		IEA		N	RGD:5509061	20111116	MGI			
11050	Pah	phenylalanine hydroxylase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11050	Pah	phenylalanine hydroxylase	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:12499868
11050	Pah	phenylalanine hydroxylase	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11050	Pah	phenylalanine hydroxylase	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11050	Pah	phenylalanine hydroxylase	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0013724	decreased circulating tyrosine level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0013724	decreased circulating tyrosine level		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11050	Pah	phenylalanine hydroxylase	gene	MP:0020446	increased NAD(P)H oxidase activity		IAGP		N	RGD:5509061	20251030	MGI			PMID:21640623
11050	Pah	phenylalanine hydroxylase	gene	MP:0020875	decreased nervous system dopamine level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0020876	increased nervous system dopamine level		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11050	Pah	phenylalanine hydroxylase	gene	MP:0030670	increased circulating phenylalanine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:8375656
11050	Pah	phenylalanine hydroxylase	gene	MP:0030670	increased circulating phenylalanine level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0030670	increased circulating phenylalanine level		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11050	Pah	phenylalanine hydroxylase	gene	MP:0030697	increased phenylalanine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:21640623
11050	Pah	phenylalanine hydroxylase	gene	MP:0030697	increased phenylalanine level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33790381
11050	Pah	phenylalanine hydroxylase	gene	MP:0030697	increased phenylalanine level		IAGP		N	RGD:5509061	20260604	MGI			PMID:33051130
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20201022	MGI			
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15869599
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20201022	MGI			
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8550840
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20200625	MGI			PMID:23919993
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747283
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15869599
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15869599
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297377
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481248
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11141484
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104787
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723219
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15869599
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696429
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897066
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897066
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297377
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17561000
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15869599
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712412
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747283
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481248
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:10712412
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747283
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747283
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15869599
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735799
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17561000
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557572
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11059781
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747283
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15869599
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20160512	MGI			PMID:25799354
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15869599
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481248
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747283
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14747283
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723219
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20160512	MGI			PMID:25799354
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897066
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0014967	increased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:17561000
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200625	MGI			PMID:23919993
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200625	MGI			PMID:23919993
11055	Serpine1	serine (or cysteine) peptidase inhibitor, clade E, member 1	gene	MP:0031414	decreased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:14747283
11056	Pam	peptidylglycine alpha-amidating monooxygenase	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16225857
11056	Pam	peptidylglycine alpha-amidating monooxygenase	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16225857
11056	Pam	peptidylglycine alpha-amidating monooxygenase	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16225857
11056	Pam	peptidylglycine alpha-amidating monooxygenase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16225857
11056	Pam	peptidylglycine alpha-amidating monooxygenase	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16225857
11056	Pam	peptidylglycine alpha-amidating monooxygenase	gene	MP:0010943	abnormal bronchus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16225857
11056	Pam	peptidylglycine alpha-amidating monooxygenase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16225857
11056	Pam	peptidylglycine alpha-amidating monooxygenase	gene	MP:0012303	umbilical vein stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16225857
11057	Reg3b	regenerating islet-derived 3 beta	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
11057	Reg3b	regenerating islet-derived 3 beta	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230601	MGI			
11057	Reg3b	regenerating islet-derived 3 beta	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
11057	Reg3b	regenerating islet-derived 3 beta	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230601	MGI			
11057	Reg3b	regenerating islet-derived 3 beta	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20141003	MGI			
11057	Reg3b	regenerating islet-derived 3 beta	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
11058	Pax1	paired box 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:8187635
11058	Pax1	paired box 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11058	Pax1	paired box 1	gene	MP:0000139	absent vertebral transverse processes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10656775
11058	Pax1	paired box 1	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11058	Pax1	paired box 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11058	Pax1	paired box 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378260
11058	Pax1	paired box 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23377878
11058	Pax1	paired box 1	gene	MP:0000454	abnormal jaw morphology		IEA		N	RGD:5509061	20111116	MGI			
11058	Pax1	paired box 1	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
11058	Pax1	paired box 1	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20111116	MGI			
11058	Pax1	paired box 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378260
11058	Pax1	paired box 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23377878
11058	Pax1	paired box 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11058	Pax1	paired box 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23377878
11058	Pax1	paired box 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11058	Pax1	paired box 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
11058	Pax1	paired box 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23377878
11058	Pax1	paired box 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
11058	Pax1	paired box 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378260
11058	Pax1	paired box 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11058	Pax1	paired box 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10656775
11058	Pax1	paired box 1	gene	MP:0002116	abnormal craniofacial bone morphology		IEA		N	RGD:5509061	20111116	MGI			
11058	Pax1	paired box 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
11058	Pax1	paired box 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633672
11058	Pax1	paired box 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23377878
11058	Pax1	paired box 1	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11058	Pax1	paired box 1	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550316
11058	Pax1	paired box 1	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550316
11058	Pax1	paired box 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10656775
11058	Pax1	paired box 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10656775
11058	Pax1	paired box 1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378260
11058	Pax1	paired box 1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
11058	Pax1	paired box 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
11058	Pax1	paired box 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
11058	Pax1	paired box 1	gene	MP:0004083	polysyndactyly		IEA		N	RGD:5509061	20111116	MGI			
11058	Pax1	paired box 1	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0004346	absent acromion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0004346	absent acromion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0004346	absent acromion		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11058	Pax1	paired box 1	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0004604	abnormal vertebral pedicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0004604	abnormal vertebral pedicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0004605	abnormal vertebral lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378260
11058	Pax1	paired box 1	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0004626	vertebral compression		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378260
11058	Pax1	paired box 1	gene	MP:0004626	vertebral compression		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0004652	small caudal vertebrae		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11058	Pax1	paired box 1	gene	MP:0004658	abnormal ventral tubercle of atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0004658	abnormal ventral tubercle of atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0004667	vertebral body hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0004668	absent vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0004668	absent vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0004668	absent vertebral body		IAGP		N	RGD:5509061	20150528	MGI			PMID:8187635
11058	Pax1	paired box 1	gene	MP:0004670	small vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20150528	MGI			PMID:8187635
11058	Pax1	paired box 1	gene	MP:0004687	split vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0005229	abnormal intervertebral disk development		IEA		N	RGD:5509061	20111116	MGI			
11058	Pax1	paired box 1	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550316
11058	Pax1	paired box 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0006295	absent sclerotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0008149	abnormal costovertebral joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0008149	abnormal costovertebral joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7875377
11058	Pax1	paired box 1	gene	MP:0008149	abnormal costovertebral joint morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:8187635
11058	Pax1	paired box 1	gene	MP:0009037	abnormal subarachnoid space development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0009929	meningomyelocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671740
11058	Pax1	paired box 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
11058	Pax1	paired box 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364424
11058	Pax1	paired box 1	gene	MP:0011400	lethality, complete penetrance		IEA		N	RGD:5509061	20150528	MGI			
11058	Pax1	paired box 1	gene	MP:0013176	abnormal tail position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093716
11058	Pax1	paired box 1	gene	MP:0013179	wavy tail		IEA		N	RGD:5509061	20150528	MGI			
11058	Pax1	paired box 1	gene	MP:0030833	small acromion		IAGP		N	RGD:5509061	20181018	MGI			PMID:10656775
11058	Pax1	paired box 1	gene	MP:0030833	small acromion		IAGP		N	RGD:5509061	20200123	MGI			PMID:24538930
11059	Pax6	paired box 6	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210826	MGI			
11059	Pax6	paired box 6	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:1684639
11059	Pax6	paired box 6	gene	MP:0000450	absent snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
11059	Pax6	paired box 6	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
11059	Pax6	paired box 6	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19474196
11059	Pax6	paired box 6	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9232602
11059	Pax6	paired box 6	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19474196
11059	Pax6	paired box 6	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548580
11059	Pax6	paired box 6	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19500363
11059	Pax6	paired box 6	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979618
11059	Pax6	paired box 6	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289327
11059	Pax6	paired box 6	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289327
11059	Pax6	paired box 6	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289327
11059	Pax6	paired box 6	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289327
11059	Pax6	paired box 6	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17942732
11059	Pax6	paired box 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548580
11059	Pax6	paired box 6	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19500363
11059	Pax6	paired box 6	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515312
11059	Pax6	paired box 6	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20111116	MGI			
11059	Pax6	paired box 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076764
11059	Pax6	paired box 6	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515312
11059	Pax6	paired box 6	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851982
11059	Pax6	paired box 6	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481423
11059	Pax6	paired box 6	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714668
11059	Pax6	paired box 6	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064680
11059	Pax6	paired box 6	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7035547
11059	Pax6	paired box 6	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789273
11059	Pax6	paired box 6	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062307
11059	Pax6	paired box 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1684639
11059	Pax6	paired box 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592925
11059	Pax6	paired box 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7035547
11059	Pax6	paired box 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649798
11059	Pax6	paired box 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9163426
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10886015
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062307
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481423
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16303964
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1684639
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19474196
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22240097
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592925
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481423
11059	Pax6	paired box 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714668
11059	Pax6	paired box 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983873
11059	Pax6	paired box 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
11059	Pax6	paired box 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
11059	Pax6	paired box 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22240097
11059	Pax6	paired box 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10886015
11059	Pax6	paired box 6	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:16303964
11059	Pax6	paired box 6	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
11059	Pax6	paired box 6	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:7035547
11059	Pax6	paired box 6	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
11059	Pax6	paired box 6	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592925
11059	Pax6	paired box 6	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
11059	Pax6	paired box 6	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:16303964
11059	Pax6	paired box 6	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:19474196
11059	Pax6	paired box 6	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:7035547
11059	Pax6	paired box 6	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20160310	MGI			PMID:6877261
11059	Pax6	paired box 6	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064680
11059	Pax6	paired box 6	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062307
11059	Pax6	paired box 6	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16303964
11059	Pax6	paired box 6	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19474196
11059	Pax6	paired box 6	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:6877261
11059	Pax6	paired box 6	gene	MP:0001317	abnormal pupil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0001317	abnormal pupil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983873
11059	Pax6	paired box 6	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062307
11059	Pax6	paired box 6	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983873
11059	Pax6	paired box 6	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983873
11059	Pax6	paired box 6	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4972360
11059	Pax6	paired box 6	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649798
11059	Pax6	paired box 6	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22240097
11059	Pax6	paired box 6	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
11059	Pax6	paired box 6	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15110714
11059	Pax6	paired box 6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210520	MGI			
11059	Pax6	paired box 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15110714
11059	Pax6	paired box 6	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19034419
11059	Pax6	paired box 6	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649798
11059	Pax6	paired box 6	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592925
11059	Pax6	paired box 6	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17660683
11059	Pax6	paired box 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17660683
11059	Pax6	paired box 6	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
11059	Pax6	paired box 6	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19500363
11059	Pax6	paired box 6	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592925
11059	Pax6	paired box 6	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9363853
11059	Pax6	paired box 6	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19500363
11059	Pax6	paired box 6	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9232602
11059	Pax6	paired box 6	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525473
11059	Pax6	paired box 6	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649798
11059	Pax6	paired box 6	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1684639
11059	Pax6	paired box 6	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17660683
11059	Pax6	paired box 6	gene	MP:0002546	mydriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983873
11059	Pax6	paired box 6	gene	MP:0002546	mydriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15110714
11059	Pax6	paired box 6	gene	MP:0002697	abnormal eye size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592925
11059	Pax6	paired box 6	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0002700	increased opacity of vitreous body		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15110714
11059	Pax6	paired box 6	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481423
11059	Pax6	paired box 6	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714668
11059	Pax6	paired box 6	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
11059	Pax6	paired box 6	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22240097
11059	Pax6	paired box 6	gene	MP:0002938	white spotting		IEA		N	RGD:5509061	20111116	MGI			
11059	Pax6	paired box 6	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0003093	abnormal cornea anterior stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0003115	abnormal respiratory system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789273
11059	Pax6	paired box 6	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210826	MGI			
11059	Pax6	paired box 6	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548580
11059	Pax6	paired box 6	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714668
11059	Pax6	paired box 6	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983873
11059	Pax6	paired box 6	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
11059	Pax6	paired box 6	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4972360
11059	Pax6	paired box 6	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15110714
11059	Pax6	paired box 6	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069887
11059	Pax6	paired box 6	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789273
11059	Pax6	paired box 6	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9232602
11059	Pax6	paired box 6	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9163426
11059	Pax6	paired box 6	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:14762144
11059	Pax6	paired box 6	gene	MP:0003687	abnormal intraocular muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4972360
11059	Pax6	paired box 6	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19500363
11059	Pax6	paired box 6	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731698
11059	Pax6	paired box 6	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19034419
11059	Pax6	paired box 6	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9224716
11059	Pax6	paired box 6	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289327
11059	Pax6	paired box 6	gene	MP:0004171	abnormal pallium development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124115
11059	Pax6	paired box 6	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064680
11059	Pax6	paired box 6	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0004224	absent trabecular meshwork		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0004226	absent Schlemm's canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069887
11059	Pax6	paired box 6	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1684639
11059	Pax6	paired box 6	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548580
11059	Pax6	paired box 6	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19474196
11059	Pax6	paired box 6	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9363853
11059	Pax6	paired box 6	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17660683
11059	Pax6	paired box 6	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525473
11059	Pax6	paired box 6	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515312
11059	Pax6	paired box 6	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
11059	Pax6	paired box 6	gene	MP:0005099	abnormal ciliary body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10451227
11059	Pax6	paired box 6	gene	MP:0005128	decreased adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19034419
11059	Pax6	paired box 6	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481423
11059	Pax6	paired box 6	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4972360
11059	Pax6	paired box 6	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20190808	MGI			PMID:22792072
11059	Pax6	paired box 6	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481423
11059	Pax6	paired box 6	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0005208	abnormal iris stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074448
11059	Pax6	paired box 6	gene	MP:0005241	abnormal retina ganglion layer morphology		IEA		N	RGD:5509061	20111116	MGI			
11059	Pax6	paired box 6	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0005261	aniridia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983873
11059	Pax6	paired box 6	gene	MP:0005261	aniridia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2173141
11059	Pax6	paired box 6	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:22240097
11059	Pax6	paired box 6	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19034419
11059	Pax6	paired box 6	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983873
11059	Pax6	paired box 6	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692153
11059	Pax6	paired box 6	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064680
11059	Pax6	paired box 6	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17051153
11059	Pax6	paired box 6	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064680
11059	Pax6	paired box 6	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076764
11059	Pax6	paired box 6	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481423
11059	Pax6	paired box 6	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
11059	Pax6	paired box 6	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692153
11059	Pax6	paired box 6	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4972360
11059	Pax6	paired box 6	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0006095	absent amacrine cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0006219	optic nerve degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983873
11059	Pax6	paired box 6	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0006243	impaired pupillary reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979618
11059	Pax6	paired box 6	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789273
11059	Pax6	paired box 6	gene	MP:0006369	supernumerary incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9363853
11059	Pax6	paired box 6	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19500363
11059	Pax6	paired box 6	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515312
11059	Pax6	paired box 6	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548580
11059	Pax6	paired box 6	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515312
11059	Pax6	paired box 6	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19474196
11059	Pax6	paired box 6	gene	MP:0008521	abnormal Bowman membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
11059	Pax6	paired box 6	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074448
11059	Pax6	paired box 6	gene	MP:0008794	increased lens epithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
11059	Pax6	paired box 6	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20210520	MGI			
11059	Pax6	paired box 6	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0008946	abnormal neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
11059	Pax6	paired box 6	gene	MP:0009174	absent pancreatic beta cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9224716
11059	Pax6	paired box 6	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15110714
11059	Pax6	paired box 6	gene	MP:0009178	absent pancreatic alpha cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9163426
11059	Pax6	paired box 6	gene	MP:0009178	absent pancreatic alpha cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9224716
11059	Pax6	paired box 6	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:9163426
11059	Pax6	paired box 6	gene	MP:0009265	delayed eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481423
11059	Pax6	paired box 6	gene	MP:0009522	submandibular gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731698
11059	Pax6	paired box 6	gene	MP:0009637	abnormal pretectal region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0009703	decreased birth body size		IEA		N	RGD:5509061	20111116	MGI			
11059	Pax6	paired box 6	gene	MP:0009725	absent lens vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0009725	absent lens vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789273
11059	Pax6	paired box 6	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515312
11059	Pax6	paired box 6	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0009859	eye opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19474196
11059	Pax6	paired box 6	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548580
11059	Pax6	paired box 6	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950124
11059	Pax6	paired box 6	gene	MP:0010259	anterior polar cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10886015
11059	Pax6	paired box 6	gene	MP:0010259	anterior polar cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0010259	anterior polar cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:6877261
11059	Pax6	paired box 6	gene	MP:0010259	anterior polar cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:9166583
11059	Pax6	paired box 6	gene	MP:0010292	increased alimentary system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17660683
11059	Pax6	paired box 6	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17660683
11059	Pax6	paired box 6	gene	MP:0010709	absent eye anterior chamber		IAGP		N	RGD:5509061	20201119	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0010713	corneal-lenticular stalk		IAGP		N	RGD:5509061	20141003	MGI			PMID:16303964
11059	Pax6	paired box 6	gene	MP:0010713	corneal-lenticular stalk		IAGP		N	RGD:5509061	20141003	MGI			PMID:22240097
11059	Pax6	paired box 6	gene	MP:0010713	corneal-lenticular stalk		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515312
11059	Pax6	paired box 6	gene	MP:0010713	corneal-lenticular stalk		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592925
11059	Pax6	paired box 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15110714
11059	Pax6	paired box 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11059	Pax6	paired box 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10451227
11059	Pax6	paired box 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1684639
11059	Pax6	paired box 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9163426
11059	Pax6	paired box 6	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592925
11059	Pax6	paired box 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649798
11059	Pax6	paired box 6	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062307
11059	Pax6	paired box 6	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
11059	Pax6	paired box 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11059	Pax6	paired box 6	gene	MP:0011102	embryonic lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11059	Pax6	paired box 6	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11059	Pax6	paired box 6	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10886015
11059	Pax6	paired box 6	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779807
11059	Pax6	paired box 6	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064680
11059	Pax6	paired box 6	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538882
11059	Pax6	paired box 6	gene	MP:0011932	abnormal endocrine pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199433
11059	Pax6	paired box 6	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20230810	MGI			PMID:19570848
11059	Pax6	paired box 6	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0012168	abnormal optic placode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714668
11059	Pax6	paired box 6	gene	MP:0012168	abnormal optic placode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0012170	absent optic placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069887
11059	Pax6	paired box 6	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0013742	absent ciliary body		IAGP		N	RGD:5509061	20150416	MGI			PMID:19563798
11059	Pax6	paired box 6	gene	MP:0013791	absent external nares		IAGP		N	RGD:5509061	20150611	MGI			PMID:11062307
11059	Pax6	paired box 6	gene	MP:0014707	increased corneal pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:15917450
11059	Pax6	paired box 6	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:12692153
11059	Pax6	paired box 6	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:12714618
11059	Pax6	paired box 6	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:17051153
11059	Pax6	paired box 6	gene	MP:0021101	abnormal ventral interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:16525473
11059	Pax6	paired box 6	gene	MP:0021102	abnormal ventral interneuron 0 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:16525473
11059	Pax6	paired box 6	gene	MP:0021103	abnormal ventral interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:14762144
11059	Pax6	paired box 6	gene	MP:0021103	abnormal ventral interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:16525473
11059	Pax6	paired box 6	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:16525473
11059	Pax6	paired box 6	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:103464
11059	Pax6	paired box 6	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:24523460
11059	Pax6	paired box 6	gene	MP:0030060	absent nasal pit		IAGP		N	RGD:5509061	20170921	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20171109	MGI			PMID:3794606
11059	Pax6	paired box 6	gene	MP:0031345	developmental cataract		IEA		N	RGD:5509061	20220217	MGI			
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009122	decreased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009128	decreased brown fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938127
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16300682
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792850
11062	Pck1	phosphoenolpyruvate carboxykinase 1, cytosolic	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:16300682
11062069	Bpq31_m	blood pressure QTL 31 (mouse)	qtl	MP:0000231	hypertension		IAGP		N	RGD:5509061	20160428	MGI			PMID:12118100
11062069	Bpq31_m	blood pressure QTL 31 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:12118100
11062078	Axtofd7_m	anxiety-open field defecation 7 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11454769
11062079	Axtofd6_m	anxiety-open field defecation 6 (mouse)	qtl	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20160428	MGI			PMID:14990867
11062079	Axtofd6_m	anxiety-open field defecation 6 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11454769
11062080	Axtofa10_m	anxiety-open field activity 10 (mouse)	qtl	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160428	MGI			PMID:14990867
11062080	Axtofa10_m	anxiety-open field activity 10 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11454769
11062081	Axtofa9_m	anxiety-open field activity 9 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20160428	MGI			PMID:14990867
11062081	Axtofa9_m	anxiety-open field activity 9 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11418486|PMID:11454769
11062082	Axtofa8_m	anxiety-open field activity 8 (mouse)	qtl	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160428	MGI			PMID:14990867
11062082	Axtofa8_m	anxiety-open field activity 8 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11454769
11063	Pcp4	Purkinje cell protein 4	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28069794
11063	Pcp4	Purkinje cell protein 4	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576365
11063	Pcp4	Purkinje cell protein 4	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576365
11063	Pcp4	Purkinje cell protein 4	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20180215	MGI			PMID:28069794
11063	Pcp4	Purkinje cell protein 4	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28069794
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0000955	abnormal spinal cord morphology		IEA		N	RGD:5509061	20141003	MGI			
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0002917	decreased synaptic depression		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0002923	increased post-tetanic potentiation		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0008025	brain vacuoles		IEA		N	RGD:5509061	20141003	MGI			
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032334
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034090
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585880
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585880
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034090
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585880
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0012314	enhanced learning		IAGP		N	RGD:5509061	20150903	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0014369	enhanced spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:26272049
11065	Pde4b	phosphodiesterase 4B, cAMP specific	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20211014	MGI			PMID:26272049
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518565
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518565
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518565
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518565
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15644445
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585880
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585880
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585880
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0009777	abnormal behavioral response to anesthetic		IAGP		N	RGD:5509061	20210513	MGI			PMID:33609559
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518565
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585880
11066	Pde4d	phosphodiesterase 4D, cAMP specific	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:10518565
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522834
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522834
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001184	absent pulmonary alveoli		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522834
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522834
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0004735	enlarged thoracic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522834
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0010822	pneumothorax		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0010900	abnormal pulmonary interalveolar septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522834
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361870
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8681381
11067	Pdgfa	platelet derived growth factor, alpha	gene	MP:0014079	decreased small intestinal villus number		IAGP		N	RGD:5509061	20160414	MGI			PMID:23938297
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169633
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331305
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20944627
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20200910	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20944627
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169633
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419690
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331305
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331305
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20944627
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419690
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169633
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20944627
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419690
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0005096	erythroblastosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331305
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331305
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12169633
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0006186	retina fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419690
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0010451	kidney microaneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0010479	brain aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011428	decreased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011428	decreased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011428	decreased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011429	absent mesangial cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958863
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897053
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0020329	decreased capillary density		IAGP		N	RGD:5509061	20160714	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0020329	decreased capillary density		IAGP		N	RGD:5509061	20160714	MGI			PMID:20944627
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0020331	increased capillary tortuosity		IAGP		N	RGD:5509061	20160714	MGI			PMID:15084468
11068	Pdgfb	platelet derived growth factor subunit B	gene	MP:0031384	impaired blood-brain barrier function		IAGP		N	RGD:5509061	20220407	MGI			PMID:20944627
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000105	impaired ossification of basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000158	absent sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000494	abnormal cecum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000924	absent roof plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568391
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23335233
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001699	increased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23938297
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002683	delayed fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002768	small adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0002990	short ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003488
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003587	ureter obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:23335233
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568391
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003939	abnormal myotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004199	increased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004202	pulmonary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004506	abnormal pubis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004508	abnormal pectoral girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004546	esophagus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0006418	abnormal testis cord formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0008856	fetal bleb		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0008856	fetal bleb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0009370	decreased theca cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568391
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490557
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0010440	anomalous pulmonary venous connection		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0010441	total anomalous pulmonary venous connection		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0010528	pulmonary vein hypoplasia		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0010548	abnormal dorsal mesocardium morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003488
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23335233
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568391
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011147	increased mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011180	abnormal hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23335233
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011185	absent primitive endoderm		IAGP		N	RGD:5509061	20160728	MGI			PMID:24835466
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011385	abnormal testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011426	abnormal ureter smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011683	dual inferior vena cava		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20170223	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0011748	intestinal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568391
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0012279	wide sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20260402	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20260402	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0013520	increased CD4-positive NK T cell number		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0013523	increased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20250508	MGI			
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0014166	ectopic cranial bone		IAGP		N	RGD:5509061	20160407	MGI			PMID:12748302
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0014808	abnormal pleuroperitoneal fold morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:17568391
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0020417	increased fibroblast chemotaxis		IAGP		N	RGD:5509061	20170223	MGI			PMID:19217431
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0030834	acromion hypoplasia		IAGP		N	RGD:5509061	20181018	MGI			PMID:9226440
11069	Pdgfra	platelet derived growth factor receptor, alpha polypeptide	gene	MP:0031138	testicular hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16690964
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000314	schistocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590688
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000445	short snout		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000484	abnormal pulmonary artery morphology		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000533	kidney hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000533	kidney hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20160915	MGI			PMID:25803852
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210826	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331305
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590688
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20160811	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124809
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20160915	MGI			PMID:25803852
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002635	reduced sensorimotor gating		IAGP		N	RGD:5509061	20160915	MGI			PMID:25803852
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037818
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002768	small adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20151001	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419690
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16690964
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419690
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0004125	abnormal venule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419690
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:16805849
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005327	abnormal mesangial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124809
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005327	abnormal mesangial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005489	vascular smooth muscle hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16690964
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590688
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331305
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331305
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0006185	retina hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0006203	eye hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0006203	eye hemorrhage		IAGP		N	RGD:5509061	20151001	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0006253	clinodactyly		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20151001	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20151001	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008137	absent podocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16805849
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10419690
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008816	petechiae		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008856	fetal bleb		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008903	abnormal mesenteric fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20160915	MGI			PMID:25803852
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0009130	increased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20160915	MGI			PMID:25803852
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782318
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0009859	eye opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0009869	abnormal descending aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0009870	abnormal abdominal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20151001	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010451	kidney microaneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010468	abnormal thoracic aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010488	abnormal left subclavian artery morphology		IEA		N	RGD:5509061	20150326	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011156	abnormal hypodermis fat layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011169	abnormal white fat cell differentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664579
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011359	decreased glomerular capillary number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011429	absent mesangial cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011437	glomerulus hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124809
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011508	abnormal glomerular capillary thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011514	skin hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14624252
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011515	purpura		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958864
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124809
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0011706	abnormal fibroblast migration		IAGP		N	RGD:5509061	20150212	MGI			PMID:15284236
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17499702
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:15284236
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0014179	abnormal blood-retina barrier function		IAGP		N	RGD:5509061	20160526	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:23633653
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:11239463
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0031138	testicular hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:19056881
11070	Pdgfrb	platelet derived growth factor receptor, beta polypeptide	gene	MP:0031510	increased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:21664579
11074	Pepc	peptidase C	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
11074	Pepc	peptidase C	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20180329	MGI			PMID:29440507
11074	Pepc	peptidase C	gene	MP:0009785	abnormal susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180329	MGI			PMID:29440507
11074	Pepc	peptidase C	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20180329	MGI			PMID:29440507
11074	Pepc	peptidase C	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:29440507
11074	Pepc	peptidase C	gene	MP:0031045	decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:29440507
11075	Pepd	peptidase D	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
11075	Pepd	peptidase D	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
11075	Pepd	peptidase D	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0000372	irregular coat pigmentation		IEA		N	RGD:5509061	20141211	MGI			
11075	Pepd	peptidase D	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220811	MGI			
11075	Pepd	peptidase D	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141211	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141218	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141218	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
11075	Pepd	peptidase D	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
11075	Pepd	peptidase D	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
11075	Pepd	peptidase D	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
11075	Pepd	peptidase D	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0002691	small stomach		IEA		N	RGD:5509061	20181227	MGI			
11075	Pepd	peptidase D	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
11075	Pepd	peptidase D	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
11075	Pepd	peptidase D	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141211	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20181227	MGI			
11075	Pepd	peptidase D	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141218	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20181227	MGI			
11075	Pepd	peptidase D	gene	MP:0003808	increased atrioventricular cushion size		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
11075	Pepd	peptidase D	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20201022	MGI			
11075	Pepd	peptidase D	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141211	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0005431	decreased oocyte number		IEA		N	RGD:5509061	20141211	MGI			
11075	Pepd	peptidase D	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
11075	Pepd	peptidase D	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141211	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20250508	MGI			
11075	Pepd	peptidase D	gene	MP:0008174	decreased follicular B cell number		IEA		N	RGD:5509061	20220811	MGI			
11075	Pepd	peptidase D	gene	MP:0008215	decreased immature B cell number		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20181227	MGI			
11075	Pepd	peptidase D	gene	MP:0009643	abnormal urine homeostasis		IEA		N	RGD:5509061	20141211	MGI			
11075	Pepd	peptidase D	gene	MP:0009923	decreased transitional stage T1 B cell number		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
11075	Pepd	peptidase D	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
11075	Pepd	peptidase D	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0010770	preweaning lethality		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0011416	abnormal testis interstitial tissue morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:18821597
11075	Pepd	peptidase D	gene	MP:0011640	abnormal aorta collagen fibril morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0011896	increased circulating unsaturated transferrin level		IEA		N	RGD:5509061	20211021	MGI			
11075	Pepd	peptidase D	gene	MP:0012076	abnormal agouti pigmentation		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0013427	increased memory-marker NK cell number		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0013430	increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0013514	increased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0013678	decreased Ly6C-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0013691	decreased CD5-positive Ly6C-positive T cell number		IEA		N	RGD:5509061	20220811	MGI			
11075	Pepd	peptidase D	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
11075	Pepd	peptidase D	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20141211	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20250911	MGI			PMID:21472842
11075	Pepd	peptidase D	gene	MP:0031609	increased fetal cardiomyocyte size		IAGP		N	RGD:5509061	20240321	MGI			PMID:21472842
11075102	Modc2_m	modifier of Odc2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160506	MGI		Created by mouse qtl pipeline	PMID:16086382
11075102	Modc2_m	modifier of Odc2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20160506	MGI		Created by mouse qtl pipeline	PMID:16086382
11075105	Modc1_m	modifier of Odc1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160506	MGI		Created by mouse qtl pipeline	PMID:11944982
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0011122	absent primordial ovarian follicles		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0011126	absent primary ovarian follicles		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0011130	absent tertiary ovarian follicles		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11081846	Redic1	regulator of DNA class I crossover intermediates 1	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
11082165	Cd300ld2	CD300 molecule like family member D2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
11082165	Cd300ld2	CD300 molecule like family member D2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
11082165	Cd300ld2	CD300 molecule like family member D2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
11082165	Cd300ld2	CD300 molecule like family member D2	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20210128	MGI			
11082585	4931422A03Rik	RIKEN cDNA 4931422A03 gene	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20250508	MGI			
11082585	4931422A03Rik	RIKEN cDNA 4931422A03 gene	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
11082585	4931422A03Rik	RIKEN cDNA 4931422A03 gene	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20211021	MGI			
11082585	4931422A03Rik	RIKEN cDNA 4931422A03 gene	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20260402	MGI			
11082585	4931422A03Rik	RIKEN cDNA 4931422A03 gene	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20250508	MGI			
11082585	4931422A03Rik	RIKEN cDNA 4931422A03 gene	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
11082585	4931422A03Rik	RIKEN cDNA 4931422A03 gene	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20250508	MGI			
11082624	Prr35	proline rich 35	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20230720	MGI			
11082624	Prr35	proline rich 35	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20230720	MGI			
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20160421	MGI			
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20201022	MGI			
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:37541209
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0002309	abnormal vital capacity		IAGP		N	RGD:5509061	20260521	MGI			PMID:37541209
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20201119	MGI			PMID:32884050
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20201119	MGI			PMID:32884050
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20160421	MGI			
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20201119	MGI			PMID:32884050
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20260521	MGI			PMID:37541209
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0010816	decreased type I pneumocyte number		IAGP		N	RGD:5509061	20260521	MGI			PMID:37541209
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0010896	decreased lung compliance		IAGP		N	RGD:5509061	20260521	MGI			PMID:37541209
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0014246	decreased cellular ATP level		IAGP		N	RGD:5509061	20260521	MGI			PMID:37541209
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20260521	MGI			PMID:37541209
11085	Pfkfb2	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	gene	MP:0031003	increased kidney glycogen level		IAGP		N	RGD:5509061	20201119	MGI			PMID:32884050
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20210909	MGI			PMID:33691103
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0002496	increased IgD level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33691103
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33691103
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33691103
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0005440	increased glycogen level		IAGP		N	RGD:5509061	20210909	MGI			PMID:33691103
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210909	MGI			PMID:33691103
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210909	MGI			PMID:33691103
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0010183	abnormal CD4-positive helper T cell morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
11087	Pgd	phosphogluconate dehydrogenase	gene	MP:0012762	abnormal alpha-beta T cell morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33691103
11091	Pgm1	phosphoglucomutase 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20251211	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20251211	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20210422	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20210422	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20210422	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210422	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251211	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20251211	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20251211	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20251211	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20230629	MGI			PMID:31077402
11091	Pgm1	phosphoglucomutase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230629	MGI			PMID:31077402
11091	Pgm1	phosphoglucomutase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230629	MGI			PMID:31077402
11091	Pgm1	phosphoglucomutase 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210520	MGI			
11091	Pgm1	phosphoglucomutase 1	gene	MP:0014134	abnormal embryo morphology		IEA		N	RGD:5509061	20251211	MGI			
11092	Pgr	progesterone receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18276762
11092	Pgr	progesterone receptor	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18276762
11092	Pgr	progesterone receptor	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21862609
11092	Pgr	progesterone receptor	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403837
11092	Pgr	progesterone receptor	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897242
11092	Pgr	progesterone receptor	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:17045797
11092	Pgr	progesterone receptor	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403837
11092	Pgr	progesterone receptor	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17941046
11092	Pgr	progesterone receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
11092	Pgr	progesterone receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11092	Pgr	progesterone receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0001123	dilated uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403837
11092	Pgr	progesterone receptor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
11092	Pgr	progesterone receptor	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11092	Pgr	progesterone receptor	gene	MP:0001376	abnormal mating receptivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
11092	Pgr	progesterone receptor	gene	MP:0001619	abnormal vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:24485460
11092	Pgr	progesterone receptor	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11092	Pgr	progesterone receptor	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0001727	abnormal embryo implantation		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
11092	Pgr	progesterone receptor	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17045797
11092	Pgr	progesterone receptor	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20190321	MGI			PMID:30626716
11092	Pgr	progesterone receptor	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
11092	Pgr	progesterone receptor	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20220512	MGI			PMID:27783953
11092	Pgr	progesterone receptor	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24485460
11092	Pgr	progesterone receptor	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20220120	MGI			PMID:31875883
11092	Pgr	progesterone receptor	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
11092	Pgr	progesterone receptor	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
11092	Pgr	progesterone receptor	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0001881	abnormal mammary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20029965
11092	Pgr	progesterone receptor	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897242
11092	Pgr	progesterone receptor	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403837
11092	Pgr	progesterone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220120	MGI			PMID:31875883
11092	Pgr	progesterone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
11092	Pgr	progesterone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
11092	Pgr	progesterone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
11092	Pgr	progesterone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976068
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403837
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868919
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17045797
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17941046
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20382891
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21508348
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23079602
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20190321	MGI			PMID:30626716
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220512	MGI			PMID:27783953
11092	Pgr	progesterone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0001928	abnormal ovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403837
11092	Pgr	progesterone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220120	MGI			PMID:31875883
11092	Pgr	progesterone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
11092	Pgr	progesterone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
11092	Pgr	progesterone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
11092	Pgr	progesterone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20160728	MGI			PMID:25377472
11092	Pgr	progesterone receptor	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:24474556
11092	Pgr	progesterone receptor	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:14667968
11092	Pgr	progesterone receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438645
11092	Pgr	progesterone receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632614
11092	Pgr	progesterone receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
11092	Pgr	progesterone receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160728	MGI			PMID:25377472
11092	Pgr	progesterone receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403837
11092	Pgr	progesterone receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16868919
11092	Pgr	progesterone receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23663785
11092	Pgr	progesterone receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25377472
11092	Pgr	progesterone receptor	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403837
11092	Pgr	progesterone receptor	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17941046
11092	Pgr	progesterone receptor	gene	MP:0002676	uterus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976068
11092	Pgr	progesterone receptor	gene	MP:0002676	uterus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403837
11092	Pgr	progesterone receptor	gene	MP:0002676	uterus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433223
11092	Pgr	progesterone receptor	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
11092	Pgr	progesterone receptor	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18026113
11092	Pgr	progesterone receptor	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438645
11092	Pgr	progesterone receptor	gene	MP:0003356	impaired luteinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0003570	increased uterus leiomyoma incidence		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11092	Pgr	progesterone receptor	gene	MP:0003572	abnormal uterus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24485460
11092	Pgr	progesterone receptor	gene	MP:0003574	abnormal oviduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24474556
11092	Pgr	progesterone receptor	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518735
11092	Pgr	progesterone receptor	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438645
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976068
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17045797
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23079602
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20190321	MGI			PMID:30626716
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220120	MGI			PMID:31875883
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220512	MGI			PMID:27783953
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220915	MGI			PMID:30213224
11092	Pgr	progesterone receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20220922	MGI			PMID:35654036
11092	Pgr	progesterone receptor	gene	MP:0003967	abnormal follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433223
11092	Pgr	progesterone receptor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976068
11092	Pgr	progesterone receptor	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18276762
11092	Pgr	progesterone receptor	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0004514	dystocia		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0004514	dystocia		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
11092	Pgr	progesterone receptor	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632614
11092	Pgr	progesterone receptor	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
11092	Pgr	progesterone receptor	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
11092	Pgr	progesterone receptor	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20160728	MGI			PMID:25377472
11092	Pgr	progesterone receptor	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518735
11092	Pgr	progesterone receptor	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
11092	Pgr	progesterone receptor	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11092	Pgr	progesterone receptor	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:30626716
11092	Pgr	progesterone receptor	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20220512	MGI			PMID:27783953
11092	Pgr	progesterone receptor	gene	MP:0004902	abnormal uterus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11092	Pgr	progesterone receptor	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
11092	Pgr	progesterone receptor	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
11092	Pgr	progesterone receptor	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11092	Pgr	progesterone receptor	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20160728	MGI			PMID:25377472
11092	Pgr	progesterone receptor	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11092	Pgr	progesterone receptor	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20160728	MGI			PMID:25377472
11092	Pgr	progesterone receptor	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632614
11092	Pgr	progesterone receptor	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11092	Pgr	progesterone receptor	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18276762
11092	Pgr	progesterone receptor	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897242
11092	Pgr	progesterone receptor	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438645
11092	Pgr	progesterone receptor	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18276762
11092	Pgr	progesterone receptor	gene	MP:0005489	vascular smooth muscle hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518735
11092	Pgr	progesterone receptor	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438645
11092	Pgr	progesterone receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438645
11092	Pgr	progesterone receptor	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18276762
11092	Pgr	progesterone receptor	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897242
11092	Pgr	progesterone receptor	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24474556
11092	Pgr	progesterone receptor	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11092	Pgr	progesterone receptor	gene	MP:0008256	abnormal myometrium morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11092	Pgr	progesterone receptor	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18276762
11092	Pgr	progesterone receptor	gene	MP:0008870	increased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0008876	decreased uterine NK cell number		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0008876	decreased uterine NK cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0008876	decreased uterine NK cell number		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0009080	uterus inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0009080	uterus inflammation		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0009088	thin uterine horn		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11092	Pgr	progesterone receptor	gene	MP:0009091	endometrium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11092	Pgr	progesterone receptor	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632614
11092	Pgr	progesterone receptor	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
11092	Pgr	progesterone receptor	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
11092	Pgr	progesterone receptor	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24474556
11092	Pgr	progesterone receptor	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11092	Pgr	progesterone receptor	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20160728	MGI			PMID:25377472
11092	Pgr	progesterone receptor	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0009094	abnormal endometrial gland morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0009094	abnormal endometrial gland morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0009094	abnormal endometrial gland morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0009094	abnormal endometrial gland morphology		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
11092	Pgr	progesterone receptor	gene	MP:0009097	absent endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:21508348
11092	Pgr	progesterone receptor	gene	MP:0009209	abnormal internal female genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24474556
11092	Pgr	progesterone receptor	gene	MP:0009251	enlarged endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0009251	enlarged endometrial glands		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0009251	enlarged endometrial glands		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18276762
11092	Pgr	progesterone receptor	gene	MP:0009352	impaired spacing of implantation sites		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0009353	twin decidual capsule		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0009360	endometrium inflammation		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21862609
11092	Pgr	progesterone receptor	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897242
11092	Pgr	progesterone receptor	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14667968
11092	Pgr	progesterone receptor	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897242
11092	Pgr	progesterone receptor	gene	MP:0009649	delayed embryo implantation		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0009662	abnormal uterine receptivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23079602
11092	Pgr	progesterone receptor	gene	MP:0009662	abnormal uterine receptivity		IAGP		N	RGD:5509061	20190321	MGI			PMID:30626716
11092	Pgr	progesterone receptor	gene	MP:0009662	abnormal uterine receptivity		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
11092	Pgr	progesterone receptor	gene	MP:0009663	abnormal uterine-embryonic axis		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0009663	abnormal uterine-embryonic axis		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0009664	abnormal luminal closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23079602
11092	Pgr	progesterone receptor	gene	MP:0009664	abnormal luminal closure		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0009666	abnormal embryo attachment		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0009666	abnormal embryo attachment		IAGP		N	RGD:5509061	20190321	MGI			PMID:30626716
11092	Pgr	progesterone receptor	gene	MP:0009666	abnormal embryo attachment		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
11092	Pgr	progesterone receptor	gene	MP:0009666	abnormal embryo attachment		IAGP		N	RGD:5509061	20220602	MGI			PMID:33590845
11092	Pgr	progesterone receptor	gene	MP:0009667	abnormal embryo invasion		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
11092	Pgr	progesterone receptor	gene	MP:0009669	abnormal postimplantation uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21508348
11092	Pgr	progesterone receptor	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20029965
11092	Pgr	progesterone receptor	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962251
11092	Pgr	progesterone receptor	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24485460
11092	Pgr	progesterone receptor	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20160728	MGI			PMID:20418913
11092	Pgr	progesterone receptor	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20160728	MGI			PMID:25377472
11092	Pgr	progesterone receptor	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20190321	MGI			PMID:30626716
11092	Pgr	progesterone receptor	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
11092	Pgr	progesterone receptor	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20220512	MGI			PMID:27783953
11092	Pgr	progesterone receptor	gene	MP:0010039	abnormal trophoblast giant cell proliferation		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0010174	decreased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897242
11092	Pgr	progesterone receptor	gene	MP:0010287	increased reproductive system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24474556
11092	Pgr	progesterone receptor	gene	MP:0011521	decreased placental labyrinth size		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
11092	Pgr	progesterone receptor	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20150611	MGI			PMID:12438645
11092	Pgr	progesterone receptor	gene	MP:0011873	enlarged uterine horn		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0011873	enlarged uterine horn		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0012008	delayed parturition		IAGP		N	RGD:5509061	20220519	MGI			PMID:35349646
11092	Pgr	progesterone receptor	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24474556
11092	Pgr	progesterone receptor	gene	MP:0013399	endometrium fibrosis		IAGP		N	RGD:5509061	20190321	MGI			PMID:30626716
11092	Pgr	progesterone receptor	gene	MP:0013400	abnormal endometrial gland development		IAGP		N	RGD:5509061	20190215	MGI			PMID:27018534
11092	Pgr	progesterone receptor	gene	MP:0013400	abnormal endometrial gland development		IAGP		N	RGD:5509061	20220203	MGI			PMID:20484741
11092	Pgr	progesterone receptor	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20141218	MGI			PMID:19439667
11092	Pgr	progesterone receptor	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20141218	MGI			PMID:20962251
11092	Pgr	progesterone receptor	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11092	Pgr	progesterone receptor	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
11092	Pgr	progesterone receptor	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11092	Pgr	progesterone receptor	gene	MP:0020253	increased collagen level		IAGP		N	RGD:5509061	20190321	MGI			PMID:30626716
11092	Pgr	progesterone receptor	gene	MP:0031336	abnormal uterine epithelium development		IAGP		N	RGD:5509061	20220120	MGI			PMID:30954472
11092	Pgr	progesterone receptor	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:10976068
11092	Pgr	progesterone receptor	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:16868919
11092	Pgr	progesterone receptor	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:20029965
11092	Pgr	progesterone receptor	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:7557380
11092	Pgr	progesterone receptor	gene	MP:0031434	increased miscarriage rate		IAGP		N	RGD:5509061	20230302	MGI			PMID:35194044
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210826	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000202	abnormal circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000203	abnormal circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001569	abnormal circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11368757
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001573	abnormal circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11368757
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002138	abnormal hepatobiliary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002139	abnormal hepatobiliary system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11368757
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930516
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002830	gallstones		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11368757
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930516
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003046	liver cirrhosis		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003254	bile duct inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003254	bile duct inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003254	bile duct inflammation		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003254	bile duct inflammation		IAGP		N	RGD:5509061	20150326	MGI			PMID:20921947
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003254	bile duct inflammation		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003256	biliary cirrhosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003328	portal hypertension		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20150326	MGI			PMID:20921947
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930516
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930516
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210128	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11368757
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11368757
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15930516
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11368757
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20150903	MGI			PMID:25478810
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005415	intrahepatic cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005415	intrahepatic cholestasis		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005415	intrahepatic cholestasis		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20210128	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210826	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210826	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20150326	MGI			PMID:20921947
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0008837	increased transforming growth factor beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0008991	abnormal bile canaliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0008991	abnormal bile canaliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0008993	abnormal portal triad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7977654
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106172
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0010877	abnormal trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0011977	abnormal sodium ion homeostasis		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0012336	decreased vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0012338	decreased bile salt level		IAGP		N	RGD:5509061	20150326	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0014476	abnormal feces lipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:15930516
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0014478	increased feces bile salt level		IAGP		N	RGD:5509061	20240704	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0014479	decreased feces bile salt level		IAGP		N	RGD:5509061	20240704	MGI			PMID:21292027
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0014963	increased circulating enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:23545228
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0020134	abnormal gallbladder size		IAGP		N	RGD:5509061	20150326	MGI			PMID:14752830
11094	Abcb4	ATP-binding cassette, sub-family B member 4	gene	MP:0021029	increased tumor necrosis factor (ligand) superfamily member 11 level		IAGP		N	RGD:5509061	20220106	MGI			PMID:23545228
11096	Phb1	prohibitin 1	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932104
11096	Phb1	prohibitin 1	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20241121	MGI			
11096	Phb1	prohibitin 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0004902	abnormal uterus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
11096	Phb1	prohibitin 1	gene	MP:0009088	thin uterine horn		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0009091	endometrium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
11096	Phb1	prohibitin 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932104
11096	Phb1	prohibitin 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11096	Phb1	prohibitin 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209023
11096	Phb1	prohibitin 1	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20231207	MGI			
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22161748
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:1962291
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:1962291
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22161748
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20220915	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713245
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751570
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976027
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172553
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22161748
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22527485
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3460077
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8266820
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1962291
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:1962291
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8266820
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22527485
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22527485
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001562	abnormal circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001565	abnormal circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:3145795
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:8266820
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751570
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1962291
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713245
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3460077
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002905	decreased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22527485
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22161748
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22527485
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3460077
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0002986	decreased urine calcium level		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172553
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:22161748
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713245
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976027
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003167	abnormal scala tympani morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976027
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003432	increased activity of parathyroid		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751570
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22161748
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22161748
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713245
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004338	small clavicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20181011	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:1962291
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:1962291
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004652	small caudal vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751570
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172553
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:22161748
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004699	unilateral deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0005628	decreased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0006025	distended Reissner membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20231130	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0006431	abnormal fibrocartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23038738
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:22161748
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:1962291
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713245
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751570
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172553
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20160310	MGI			PMID:15976027
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0009877	exostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0010110	abnormal renal phosphate reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172553
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20220915	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0011221	decreased intestinal calcium absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:8266820
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449303
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0011447	abnormal renal glucose reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:3460077
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0011470	increased urine creatinine level		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0011476	abnormal urine nucleotide level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3460077
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0011504	abnormal limb long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0011505	camptomelia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573557
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289812
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0012336	decreased vitamin D level		IAGP		N	RGD:5509061	20181004	MGI			PMID:29735309
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0013942	enthesitis		IAGP		N	RGD:5509061	20160310	MGI			PMID:23038738
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0014104	decreased chondrocyte apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:15029877
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:22527485
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:11159866
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0021186	decreased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:17710565
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0030484	abnormal osteocyte lacuna morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:18172553
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0030485	abnormal osteocyte lacunocanalicular system morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:18172553
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0030828	abnormal obturator foramen morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0030830	abnormal acetabulum morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0030876	abnormal costochondral joint morphology		IAGP		N	RGD:5509061	20181101	MGI			PMID:12414538
11097	Phex	phosphate regulating endopeptidase homolog, X-linked	gene	MP:0031060	decreased circulating C-reactive protein level		IAGP		N	RGD:5509061	20200618	MGI			PMID:29735309
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377440
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20190822	MGI			PMID:31232685
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10092065
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692150
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535627
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10092065
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10092065
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001124	abnormal gametes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692150
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207103
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207103
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207103
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:15304084
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207103
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535627
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535627
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535627
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20190530	MGI			PMID:15304084
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377440
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10092065
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10092065
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20190530	MGI			PMID:19679885
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207103
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692150
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535627
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10092065
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20190822	MGI			PMID:31232685
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10556176
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20190530	MGI			PMID:19679885
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10556176
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10556176
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20190530	MGI			PMID:15304084
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535627
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10556176
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10377440
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0003950	abnormal plasma membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8611683
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20190822	MGI			PMID:31232685
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20190530	MGI			PMID:15304084
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:19679885
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0009608	abnormal epidermal lamellar body morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:15304084
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20190530	MGI			PMID:19679885
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207103
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10556176
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10092065
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8611683
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0031010	failure of sperm-egg fusion		IAGP		N	RGD:5509061	20200130	MGI			PMID:12692150
11100	Piga	phosphatidylinositol glycan anchor biosynthesis, class A	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:10556176
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594279
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0000501	abnormal digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17056558
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594279
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510081
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510081
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10553061
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594279
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16569672
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16569672
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510081
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594279
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510081
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10553061
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594279
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510081
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10553061
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594279
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15770700
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16569672
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17056558
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10553061
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15770700
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15770700
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17056558
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0008401	abnormal CD8-positive, alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15770700
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16569672
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16569672
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0008895	abnormal intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15770700
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510081
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0010223	abnormal immunoglobulin transcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10510081
11102	Pigr	polymeric immunoglobulin receptor	gene	MP:0010223	abnormal immunoglobulin transcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594279
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062485
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988280
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:21398281
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354682
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062485
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888854
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354682
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888855
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062485
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673165
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888854
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673165
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354682
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227599
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888854
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16114097
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062485
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673165
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988280
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227599
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062485
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673165
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988280
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062485
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227599
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0004978	decreased B-1 B cell number		IEA		N	RGD:5509061	20180215	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888854
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16114097
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888854
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888855
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062485
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673165
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673165
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988280
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029981
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20180215	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20180215	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20180215	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008170	decreased B-1b cell number		IEA		N	RGD:5509061	20180215	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354682
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20180215	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888854
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354682
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888854
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354682
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888854
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888855
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354682
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:21398281
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354682
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673165
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062485
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:21398281
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20180215	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19029981
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20180215	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888855
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0011089	perinatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354682
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062485
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200109	MGI			PMID:21398281
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0014989	impaired erythropoiesis		IEA		N	RGD:5509061	20260514	MGI			
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0020359	abnormal ribbon synapse morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:21398281
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:9988280
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20190215	MGI			PMID:26974159
11103	Pik3r1	phosphoinositide-3-kinase regulatory subunit 1	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:9988280
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8233823
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0001588	abnormal hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8233823
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509290
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7689870
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8361211
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:8233823
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0003133	increased early pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11104	Pim1	Pim1, proto-oncogene, serine/threonine kinase	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199164
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180111	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20180111	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20180111	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000103	nasal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000276	heart right ventricle hypertrophy		IEA		N	RGD:5509061	20141003	MGI			
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095915
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000299	failure of atrioventricular cushion closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000608	dissociated hepatocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000757	herniated abdominal wall		IEA		N	RGD:5509061	20250508	MGI			
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677526
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001784	abnormal fluid regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579506
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579506
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385665
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677526
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095915
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928412
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677526
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579506
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385665
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151203	MGI			PMID:25574838
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20075061
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562878
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23236168
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255143
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677526
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20141003	MGI			
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928412
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932118
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:23439951
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20075061
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23236168
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003254	bile duct inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003266	biliary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003325	decreased liver function		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579506
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928412
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932118
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003334	pancreas fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677526
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12007403
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579506
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928412
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003338	pancreas lipomatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579360
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003432	increased activity of parathyroid		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003450	enlarged pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003602	increased renal hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677526
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12007403
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095915
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514735
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579506
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928412
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932118
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20075061
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20240328	MGI			PMID:37953472
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579360
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932118
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20151203	MGI			PMID:25574838
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20260430	MGI			PMID:41507385
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20075061
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004020	polyhydramnios		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004020	polyhydramnios		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579506
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004020	polyhydramnios		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301212
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004020	polyhydramnios		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385665
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004020	polyhydramnios		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004044	aortic dissection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385665
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20180111	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004451	short presphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20180111	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004967	abnormal kidney epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514735
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932118
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005328	abnormal circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988265
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23236168
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16400024
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20075061
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23236168
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20151203	MGI			PMID:25574838
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20180726	MGI			PMID:21465620
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0006278	aortic aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496422
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0006357	abnormal circulating mineral level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932118
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385665
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579360
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562878
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23236168
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23439951
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20151203	MGI			PMID:25574838
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20180726	MGI			PMID:21465620
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20260430	MGI			PMID:41507385
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009145	abnormal pancreatic acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009164	exocrine pancreas atrophy		IAGP		N	RGD:5509061	20150611	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009495	abnormal common bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009644	uremia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959710
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0010656	thick myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0010962	decreased compact bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263604
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579360
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385665
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15579506
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932118
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003909
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255143
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677526
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11593033
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12007403
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928412
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19774080
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385665
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689485
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095915
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385665
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326937
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011344	abnormal loop of Henle ascending limb thick segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20075061
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:21685914
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20180726	MGI			PMID:21465620
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20151203	MGI			PMID:25574838
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932118
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20075061
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20180222	MGI			PMID:21685914
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20180726	MGI			PMID:21465620
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20240328	MGI			PMID:37953472
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0011744	abnormal kidney epithelial cell primary cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514735
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0012172	abnormal amniotic fluid composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301212
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0014010	abnormal peroxisome morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0020382	increased kidney epithelial cell primary cilium length		IAGP		N	RGD:5509061	20161013	MGI			PMID:23064367
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0030438	increased osteoblast proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:23029375
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0030444	premature cranial synchondrosis closure		IAGP		N	RGD:5509061	20180111	MGI			PMID:18579360
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0030445	abnormal sphenooccipital synchondrosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0030446	premature sphenooccipital synchondrosis closure		IAGP		N	RGD:5509061	20180111	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0030447	abnormal presphenoid synchondrosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:18652813
11105	Pkd1	polycystin 1, transient receptor potential channel interacting	gene	MP:0030448	premature presphenoid synchondrosis closure		IAGP		N	RGD:5509061	20180111	MGI			PMID:18652813
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595440
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23078545
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17466543
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23078545
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595440
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7579416
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10886019
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595440
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23078545
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595440
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17466543
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23078545
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17466543
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7579416
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23078545
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595440
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17466543
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20240125	MGI			PMID:35988463
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0005286	decreased saturated fatty acids level		IAGP		N	RGD:5509061	20240125	MGI			PMID:35988463
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7579416
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998386
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20240125	MGI			PMID:35988463
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0010035	increased erythrocyte clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17466543
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17466543
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492793
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0014990	enhanced erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:17466543
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0020583	decreased ceramide level		IAGP		N	RGD:5509061	20240125	MGI			PMID:35988463
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:23078545
11113	Pklr	pyruvate kinase liver and red blood cell	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20240125	MGI			PMID:35988463
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808451
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11249852
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931664
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931664
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808451
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832165
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403693
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403692
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403693
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996660
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403692
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808451
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12045263
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11249852
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0003033	abnormal pulmonary vascular resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12045263
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:11249852
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403693
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808451
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12045263
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808451
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996660
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808451
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15033900
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808451
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172261
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:12045263
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996660
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0005462	abnormal mast cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220374
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403692
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403693
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403693
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274413
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172261
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172261
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172261
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220374
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832165
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20191017	MGI			PMID:24297180
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11249852
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808451
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0010936	decreased airway resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403692
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0011452	decreased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9832165
11116	Pla2g4a	phospholipase A2, group IVA (cytosolic, calcium-dependent)	gene	MP:0012010	parturition failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403692
11120	Plcb4	phospholipase C, beta 4	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9305844
11120	Plcb4	phospholipase C, beta 4	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9305844
11120	Plcb4	phospholipase C, beta 4	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9305844
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9305844
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20181227	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9305844
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861037
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9305844
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861037
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9305844
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861037
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:11551922
11120	Plcb4	phospholipase C, beta 4	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962098
11120	Plcb4	phospholipase C, beta 4	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230601	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861037
11120	Plcb4	phospholipase C, beta 4	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11551922
11120	Plcb4	phospholipase C, beta 4	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:9305844
11120	Plcb4	phospholipase C, beta 4	gene	MP:0003894	abnormal Purkinje cell innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9861037
11120	Plcb4	phospholipase C, beta 4	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962098
11120	Plcb4	phospholipase C, beta 4	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20181227	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20181227	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20181227	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
11120	Plcb4	phospholipase C, beta 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9305844
11120	Plcb4	phospholipase C, beta 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
11121	Plk1	polo like kinase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
11121	Plk1	polo like kinase 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794363
11121	Plk1	polo like kinase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
11121	Plk1	polo like kinase 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
11123	Plp2	proteolipid protein 2	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20161027	MGI			PMID:26512060
11123	Plp2	proteolipid protein 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:26512060
11123	Plp2	proteolipid protein 2	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20161027	MGI			PMID:26512060
11123	Plp2	proteolipid protein 2	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:26512060
11123	Plp2	proteolipid protein 2	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20161027	MGI			PMID:26512060
11123	Plp2	proteolipid protein 2	gene	MP:0030949	abnormal Golgi vesicle transport		IAGP		N	RGD:5509061	20190725	MGI			PMID:26512060
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258617
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:3388045
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:6313869
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581450
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20180412	MGI			PMID:22527485
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539699
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9147228
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581450
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539699
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000756	forelimb paralysis		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539699
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703401
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755691
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:6313869
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581450
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9147228
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9219937
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932191
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363066
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:3388045
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9219937
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581450
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539699
11125	Pmp22	peripheral myelin protein 22	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9147228
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755691
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17701891
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3388045
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6313869
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9147228
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9219937
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539699
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001393	ataxia		IEA		N	RGD:5509061	20141003	MGI			
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17701891
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:3388045
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:6313869
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9147228
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9219937
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539699
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6681440
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581450
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539699
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539699
11125	Pmp22	peripheral myelin protein 22	gene	MP:0001967	deafness		IEA		N	RGD:5509061	20141003	MGI			
11125	Pmp22	peripheral myelin protein 22	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:6313869
11125	Pmp22	peripheral myelin protein 22	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:6681440
11125	Pmp22	peripheral myelin protein 22	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20180412	MGI			PMID:22527485
11125	Pmp22	peripheral myelin protein 22	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581450
11125	Pmp22	peripheral myelin protein 22	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363066
11125	Pmp22	peripheral myelin protein 22	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581450
11125	Pmp22	peripheral myelin protein 22	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436605
11125	Pmp22	peripheral myelin protein 22	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17701891
11125	Pmp22	peripheral myelin protein 22	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581450
11125	Pmp22	peripheral myelin protein 22	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20160714	MGI			PMID:12090404
11125	Pmp22	peripheral myelin protein 22	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15748170
11125	Pmp22	peripheral myelin protein 22	gene	MP:0006325	impaired hearing		IEA		N	RGD:5509061	20141003	MGI			
11125	Pmp22	peripheral myelin protein 22	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174099
11125	Pmp22	peripheral myelin protein 22	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:6681440
11125	Pmp22	peripheral myelin protein 22	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581450
11125	Pmp22	peripheral myelin protein 22	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12359155
11125	Pmp22	peripheral myelin protein 22	gene	MP:0010742	increased Schwann cell number		IAGP		N	RGD:5509061	20160714	MGI			PMID:12090404
11125	Pmp22	peripheral myelin protein 22	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539699
11125	Pmp22	peripheral myelin protein 22	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20160714	MGI			PMID:12090404
11125	Pmp22	peripheral myelin protein 22	gene	MP:0011904	abnormal Schwann cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755691
11125	Pmp22	peripheral myelin protein 22	gene	MP:0011906	increased Schwann cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755691
11125	Pmp22	peripheral myelin protein 22	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20141003	MGI			
11125	Pmp22	peripheral myelin protein 22	gene	MP:0012051	spasticity		IEA		N	RGD:5509061	20141003	MGI			
11125	Pmp22	peripheral myelin protein 22	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20160714	MGI			PMID:12090404
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17698731
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:17698731
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22706789
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:17698731
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0005406	abnormal heart size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17698731
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160421	MGI			
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0012575	increased noradrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:15517585
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0012575	increased noradrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:17698731
11126	Pnmt	phenylethanolamine-N-methyltransferase	gene	MP:0030762	decreased adrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:15517585
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0009309	increased small intestine adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0009314	increased colon adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11127	Pole	polymerase (DNA directed), epsilon	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805137
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250918	MGI			PMID:36427334
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556738
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:11718806
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20250918	MGI			PMID:36427334
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16577229
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20250918	MGI			PMID:36427334
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0003879	abnormal hair cell physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556738
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004367	abnormal strial intermediate cell morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004413	absent cochlear microphonics		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004466	short cochlear outer hair cells		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20250918	MGI			PMID:36427334
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9300691
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7075549
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20250918	MGI			PMID:36427334
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7285859
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7285859
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20250918	MGI			PMID:36427334
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008330	absent somatotrophs		IAGP		N	RGD:5509061	20141003	MGI			PMID:6194978
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008330	absent somatotrophs		IAGP		N	RGD:5509061	20250918	MGI			PMID:36427334
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008333	absent lactotrophs		IAGP		N	RGD:5509061	20141003	MGI			PMID:6194978
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008333	absent lactotrophs		IAGP		N	RGD:5509061	20141003	MGI			PMID:7075549
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008338	decreased thyrotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:13819893
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008365	adenohypophysis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556738
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20250918	MGI			PMID:36427334
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008938	decreased pituitary gland weight		IAGP		N	RGD:5509061	20250918	MGI			PMID:36427334
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:16577229
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9779941
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220519	MGI			
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0011968	decreased threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840860
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0013344	increased pituitary gland apoptosis		IAGP		N	RGD:5509061	20141211	MGI			PMID:16556738
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0013808	abnormal tunnel of Corti morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0013961	abnormal Hensen stripe morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0014091	abnormal tectorial membrane striated-sheet matrix morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20190704	MGI			PMID:19176829
11129	Pou1f1	POU domain, class 1, transcription factor 1	gene	MP:0030494	abnormal molar root morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:16577229
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20260402	MGI			
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20260402	MGI			
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0003249	increased muscle free fatty acids level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0009132	abnormal white fat cell size		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0014396	decreased fat cell mitochondrial DNA content		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0014398	abnormal fat cell mitochondrial morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11130	Ppa1	pyrophosphatase (inorganic) 1	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20260122	MGI			PMID:33722839
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20250508	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0000495	abnormal colon morphology		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20260402	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002731	megacolon		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230119	MGI			
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11131	Ppia	peptidylprolyl isomerase A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308100
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735444
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773574
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735444
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735444
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9084440
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0002987	abnormal urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735444
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735444
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8627154
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735444
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735444
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735444
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8627154
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8627154
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8627154
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773574
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773574
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773574
11134	Ppp3ca	protein phosphatase 3, catalytic subunit, alpha isoform	gene	MP:0011471	decreased urine creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16735444
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11904392
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773574
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648267
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091710
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20240523	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091710
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11904392
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648267
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0002619	abnormal lymphocyte morphology		IEA		N	RGD:5509061	20190418	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20170601	MGI			PMID:27114035
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648267
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20240523	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IEA		N	RGD:5509061	20161201	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11904392
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648267
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11904392
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648267
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091710
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091710
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648267
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20170601	MGI			PMID:27114035
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648267
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20240523	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648267
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0008037	abnormal T cell morphology		IEA		N	RGD:5509061	20190418	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20240523	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091710
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773574
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0009405	increased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773574
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773574
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20170601	MGI			PMID:27114035
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20170601	MGI			PMID:27114035
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0010766	abnormal NK cell physiology		IEA		N	RGD:5509061	20161201	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0010839	decreased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20180215	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20240523	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0011822	increased CD8-positive, alpha-beta memory T cell proliferation		IEA		N	RGD:5509061	20161201	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0013519	decreased CD4-positive NK T cell number		IEA		N	RGD:5509061	20240523	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0013522	decreased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20240523	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20240523	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20240523	MGI			
11135	Ppp3cb	protein phosphatase 3, catalytic subunit, beta isoform	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20161201	MGI			
11138	Ppy	pancreatic polypeptide	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
11138	Ppy	pancreatic polypeptide	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0009568	abnormal red blood cell deformability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0010035	increased erythrocyte clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11139	Prkag1	protein kinase, AMP-activated, gamma 1 non-catalytic subunit	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881209
11140	Prkar1b	protein kinase, cAMP dependent regulatory, type I beta	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548807
11140	Prkar1b	protein kinase, cAMP dependent regulatory, type I beta	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568030
11140	Prkar1b	protein kinase, cAMP dependent regulatory, type I beta	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9295392
11140	Prkar1b	protein kinase, cAMP dependent regulatory, type I beta	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:9295392
11140	Prkar1b	protein kinase, cAMP dependent regulatory, type I beta	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9295392
11147	Prkcg	protein kinase C, gamma	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20220224	MGI			PMID:33478986
11147	Prkcg	protein kinase C, gamma	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10979601
11147	Prkcg	protein kinase C, gamma	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20220224	MGI			PMID:33478986
11147	Prkcg	protein kinase C, gamma	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20220224	MGI			PMID:33478986
11147	Prkcg	protein kinase C, gamma	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20220224	MGI			PMID:33478986
11147	Prkcg	protein kinase C, gamma	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8269510
11147	Prkcg	protein kinase C, gamma	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8269510
11147	Prkcg	protein kinase C, gamma	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8269509
11147	Prkcg	protein kinase C, gamma	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7731960
11147	Prkcg	protein kinase C, gamma	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:7731960
11147	Prkcg	protein kinase C, gamma	gene	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:11606660
11147	Prkcg	protein kinase C, gamma	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16106361
11147	Prkcg	protein kinase C, gamma	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20220224	MGI			PMID:33478986
11147	Prkcg	protein kinase C, gamma	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7731960
11147	Prkcg	protein kinase C, gamma	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392936
11147	Prkcg	protein kinase C, gamma	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:33478986
11147	Prkcg	protein kinase C, gamma	gene	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195808
11147	Prkcg	protein kinase C, gamma	gene	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195808
11147	Prkcg	protein kinase C, gamma	gene	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20141003	MGI			PMID:7731960
11147	Prkcg	protein kinase C, gamma	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20141003	MGI			PMID:11606660
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0000505	decreased digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11149	Prkg2	protein kinase, cGMP-dependent, type II	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8953039
11152	Prl	prolactin	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12399440
11152	Prl	prolactin	gene	MP:0000635	pituitary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12399440
11152	Prl	prolactin	gene	MP:0000636	enlarged pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12399440
11152	Prl	prolactin	gene	MP:0000636	enlarged pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0001746	abnormal pituitary secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12399440
11152	Prl	prolactin	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0003371	decreased circulating estrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12399440
11152	Prl	prolactin	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12399440
11152	Prl	prolactin	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0008325	abnormal gonadotroph morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12399440
11152	Prl	prolactin	gene	MP:0008332	decreased lactotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0008939	increased pituitary gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724019
11152	Prl	prolactin	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0009007	short estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0009014	prolonged proestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384572
11152	Prl	prolactin	gene	MP:0013336	pituitary gland hypertrophy		IAGP		N	RGD:5509061	20141204	MGI			PMID:12399440
11152	Prl	prolactin	gene	MP:0031362	decreased prostate gland ventral lobe weight		IAGP		N	RGD:5509061	20220303	MGI			PMID:9724019
11153	Prl4a1	prolactin family 4, subfamily a, member 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545614
11153	Prl4a1	prolactin family 4, subfamily a, member 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545614
11153	Prl4a1	prolactin family 4, subfamily a, member 1	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545614
11153	Prl4a1	prolactin family 4, subfamily a, member 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545614
11153	Prl4a1	prolactin family 4, subfamily a, member 1	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545614
11153	Prl4a1	prolactin family 4, subfamily a, member 1	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545614
11157	Prlr	prolactin receptor	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886812
11157	Prlr	prolactin receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11356702
11157	Prlr	prolactin receptor	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11356702
11157	Prlr	prolactin receptor	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445538
11157	Prlr	prolactin receptor	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166330
11157	Prlr	prolactin receptor	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810576
11157	Prlr	prolactin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159821
11157	Prlr	prolactin receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133844
11157	Prlr	prolactin receptor	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751488
11157	Prlr	prolactin receptor	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0001562	abnormal circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886812
11157	Prlr	prolactin receptor	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810576
11157	Prlr	prolactin receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810576
11157	Prlr	prolactin receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0002832	coarse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:11356702
11157	Prlr	prolactin receptor	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886812
11157	Prlr	prolactin receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886812
11157	Prlr	prolactin receptor	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897695
11157	Prlr	prolactin receptor	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0004015	abnormal oviduct environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886812
11157	Prlr	prolactin receptor	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0004909	increased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810576
11157	Prlr	prolactin receptor	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886812
11157	Prlr	prolactin receptor	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886812
11157	Prlr	prolactin receptor	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886812
11157	Prlr	prolactin receptor	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897695
11157	Prlr	prolactin receptor	gene	MP:0005248	abnormal Harderian gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11133844
11157	Prlr	prolactin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897695
11157	Prlr	prolactin receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0005471	decreased thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166330
11157	Prlr	prolactin receptor	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166330
11157	Prlr	prolactin receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159821
11157	Prlr	prolactin receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9886812
11157	Prlr	prolactin receptor	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159821
11157	Prlr	prolactin receptor	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0008779	abnormal maternal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751488
11157	Prlr	prolactin receptor	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897695
11157	Prlr	prolactin receptor	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11897695
11157	Prlr	prolactin receptor	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810576
11157	Prlr	prolactin receptor	gene	MP:0009287	decreased abdominal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159821
11157	Prlr	prolactin receptor	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12511652
11157	Prlr	prolactin receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15388648
11157	Prlr	prolactin receptor	gene	MP:0010346	increased thyroid carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166330
11157	Prlr	prolactin receptor	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0011988	increased mating frequency		IAGP		N	RGD:5509061	20240627	MGI			PMID:9009200
11157	Prlr	prolactin receptor	gene	MP:0013476	abnormal Harderian gland porphyrin secretion		IAGP		N	RGD:5509061	20150212	MGI			PMID:11133844
11157	Prlr	prolactin receptor	gene	MP:0031364	increased prostate gland ventral lobe weight		IAGP		N	RGD:5509061	20220303	MGI			PMID:12810576
11158	Prm1	protamine 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20180719	MGI			PMID:11326282
11158	Prm1	protamine 1	gene	MP:0005410	abnormal fertilization		IAGP		N	RGD:5509061	20180719	MGI			PMID:11326282
11158	Prm1	protamine 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20180719	MGI			PMID:11326282
11158	Prm1	protamine 1	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:11326282
11159	Prm2	protamine 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11326282
11159	Prm2	protamine 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620939
11159	Prm2	protamine 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220407	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230413	MGI			PMID:32727081
11159	Prm2	protamine 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220407	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20230413	MGI			PMID:32727081
11159	Prm2	protamine 2	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20220407	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20230413	MGI			PMID:32727081
11159	Prm2	protamine 2	gene	MP:0005410	abnormal fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11326282
11159	Prm2	protamine 2	gene	MP:0005410	abnormal fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620939
11159	Prm2	protamine 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11326282
11159	Prm2	protamine 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620939
11159	Prm2	protamine 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:32727081
11159	Prm2	protamine 2	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20220407	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:32727081
11159	Prm2	protamine 2	gene	MP:0009235	small sperm head		IAGP		N	RGD:5509061	20230413	MGI			PMID:32727081
11159	Prm2	protamine 2	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20230413	MGI			PMID:32727081
11159	Prm2	protamine 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0014803	abnormal flagellar waveform		IAGP		N	RGD:5509061	20251120	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220407	MGI			PMID:27833122
11159	Prm2	protamine 2	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:11326282
11160	Prnp	prion protein	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038218
11160	Prnp	prion protein	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161660
11160	Prnp	prion protein	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17709374
11160	Prnp	prion protein	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11179214
11160	Prnp	prion protein	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15351724
11160	Prnp	prion protein	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619325
11160	Prnp	prion protein	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8635458
11160	Prnp	prion protein	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20190307	MGI			PMID:27440899
11160	Prnp	prion protein	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11179214
11160	Prnp	prion protein	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8606772
11160	Prnp	prion protein	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11179214
11160	Prnp	prion protein	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11179214
11160	Prnp	prion protein	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10525406
11160	Prnp	prion protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11179214
11160	Prnp	prion protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15351724
11160	Prnp	prion protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038218
11160	Prnp	prion protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19675240
11160	Prnp	prion protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619325
11160	Prnp	prion protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8606772
11160	Prnp	prion protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8606772
11160	Prnp	prion protein	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19675240
11160	Prnp	prion protein	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8035877
11160	Prnp	prion protein	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038218
11160	Prnp	prion protein	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619325
11160	Prnp	prion protein	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19675240
11160	Prnp	prion protein	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038218
11160	Prnp	prion protein	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17709374
11160	Prnp	prion protein	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15007175
11160	Prnp	prion protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161660
11160	Prnp	prion protein	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19038218
11160	Prnp	prion protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19675240
11160	Prnp	prion protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8698234
11160	Prnp	prion protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11179214
11160	Prnp	prion protein	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17709374
11160	Prnp	prion protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8698234
11160	Prnp	prion protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:27440899
11160	Prnp	prion protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11179214
11160	Prnp	prion protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16219759
11160	Prnp	prion protein	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15007175
11160	Prnp	prion protein	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:12456643
11160	Prnp	prion protein	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:8035877
11160	Prnp	prion protein	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8698234
11160	Prnp	prion protein	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20160428	MGI			PMID:12456643
11160	Prnp	prion protein	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20190307	MGI			PMID:27440899
11160	Prnp	prion protein	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0002911	abnormal inhibitory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:8035877
11160	Prnp	prion protein	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:8035877
11160	Prnp	prion protein	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0003314	dysmetria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619325
11160	Prnp	prion protein	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:19675240
11160	Prnp	prion protein	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:20445063
11160	Prnp	prion protein	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20445063
11160	Prnp	prion protein	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8698234
11160	Prnp	prion protein	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823413
11160	Prnp	prion protein	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16492732
11160	Prnp	prion protein	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8698234
11160	Prnp	prion protein	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0003952	abnormal copper level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161660
11160	Prnp	prion protein	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16492732
11160	Prnp	prion protein	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633630
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15170227
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15354287
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16480953
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17709374
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:2890436
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7494265
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20200416	MGI			PMID:11823413
11160	Prnp	prion protein	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20200416	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633630
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16480953
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17709374
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:2890436
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8635458
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8698234
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20160428	MGI			PMID:12456643
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20190307	MGI			PMID:27440899
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20200416	MGI			PMID:11823413
11160	Prnp	prion protein	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20200416	MGI			PMID:17270731
11160	Prnp	prion protein	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15007175
11160	Prnp	prion protein	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19675240
11160	Prnp	prion protein	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0008232	abnormal cingulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20250227	MGI			PMID:39087478
11160	Prnp	prion protein	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072968
11160	Prnp	prion protein	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11823413
11160	Prnp	prion protein	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16492732
11160	Prnp	prion protein	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517717
11160	Prnp	prion protein	gene	MP:0011149	abnormal hippocampus stratum lacunosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073920
11160	Prnp	prion protein	gene	MP:0011214	increased brain copper level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14511115
11160	Prnp	prion protein	gene	MP:0011215	decreased brain copper level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14511115
11160	Prnp	prion protein	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0011979	abnormal magnesium ion homeostasis		IAGP		N	RGD:5509061	20161201	MGI			PMID:14511115
11160	Prnp	prion protein	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20161013	MGI			PMID:19709627
11160	Prnp	prion protein	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:19666958
11160	Prnp	prion protein	gene	MP:0014638	increased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:23959875
11160	Prnp	prion protein	gene	MP:0020187	abnormal susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581259
11160	Prnp	prion protein	gene	MP:0020187	abnormal susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462739
11161	Proc	protein C	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749569
11161	Proc	protein C	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749569
11161	Proc	protein C	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749569
11161	Proc	protein C	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0002343	abnormal lymph node cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749569
11161	Proc	protein C	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749569
11161	Proc	protein C	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0009275	bruising		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0010178	increased number of Howell-Jolly bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749569
11161	Proc	protein C	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0031051	lymph node hemorrhage		IAGP		N	RGD:5509061	20200618	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0031126	gangrene		IAGP		N	RGD:5509061	20200917	MGI			PMID:11159184
11161	Proc	protein C	gene	MP:0031167	abnormal lung thrombosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:9788960
11161	Proc	protein C	gene	MP:0031168	abnormal brain thrombosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:9788960
11166	Prph	peripherin	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12065660
11166	Prph	peripherin	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12065660
11168	Prps2	phosphoribosyl pyrophosphate synthetase 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24855946
11168	Prps2	phosphoribosyl pyrophosphate synthetase 2	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20150827	MGI			PMID:24855946
11168	Prps2	phosphoribosyl pyrophosphate synthetase 2	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20150827	MGI			PMID:24855946
11168	Prps2	phosphoribosyl pyrophosphate synthetase 2	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20150827	MGI			PMID:24855946
11178	Psap	prosaposin	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726558
11178	Psap	prosaposin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726558
11178	Psap	prosaposin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726558
11178	Psap	prosaposin	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726558
11178	Psap	prosaposin	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810822
11178	Psap	prosaposin	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726558
11178	Psap	prosaposin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810822
11178	Psap	prosaposin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743835
11178	Psap	prosaposin	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345707
11178	Psap	prosaposin	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0002809	increased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21700325
11178	Psap	prosaposin	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0003382	straub tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726558
11178	Psap	prosaposin	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726558
11178	Psap	prosaposin	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0004302	abnormal Deiters cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0004632	abnormal cochlear OHC efferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0004633	abnormal cochlear IHC efferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0004746	abnormal cochlear IHC afferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0004757	abnormal distal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0004962	decreased prostate gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0005180	abnormal circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105903
11178	Psap	prosaposin	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0005302	neurogenic bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20251030	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0008285	abnormal hippocampus granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480170
11178	Psap	prosaposin	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015957
11178	Psap	prosaposin	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20141003	MGI			PMID:9678511
11178	Psap	prosaposin	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810822
11178	Psap	prosaposin	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8776585
11178	Psap	prosaposin	gene	MP:0011617	abnormal habituation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446636
11178	Psap	prosaposin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0014062	nervous system inclusion bodies		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20240405	MGI			PMID:17167097
11178	Psap	prosaposin	gene	MP:0014606	dark spleen		IAGP		N	RGD:5509061	20250206	MGI			PMID:17353235
11178	Psap	prosaposin	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:11371512
11178	Psap	prosaposin	gene	MP:0020261	increased beta-galactosidase level		IAGP		N	RGD:5509061	20200806	MGI			PMID:20175216
11178	Psap	prosaposin	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:23446636
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600282
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0001836	abnormal antigen presentation via MHC class I		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0001841	decreased level of surface class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11169961
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11169961
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782352
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600282
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0002453	abnormal B lymphocyte antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782352
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11782352
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600282
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11169961
11180	Psmb9	proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2)	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:7600282
11181	Pspn	persephin	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093930
11181	Pspn	persephin	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093930
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0000362	decreased mast cell histamine storage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20211118	MGI			PMID:33972431
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892701
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283118
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0008020	abnormal dermal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20211118	MGI			PMID:33972431
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0010281	increased nervous system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0010311	increased meningioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
11182	Ptgds	prostaglandin D2 synthase (brain)	gene	MP:0010313	increased osteoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0000532	kidney vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20241121	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20241121	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210128	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20201022	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20201022	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210128	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0003918	decreased kidney weight		IEA		N	RGD:5509061	20201022	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0003946	renal necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0005238	increased brain size		IEA		N	RGD:5509061	20210128	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20210128	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0009814	increased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0009818	abnormal thromboxane level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0009871	abnormal aorta tunica adventitia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0010468	abnormal thoracic aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11183	Ptgis	prostaglandin I2 (prostacyclin) synthase	gene	MP:0011423	kidney cortex atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12403673
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883230
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699263
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17219415
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20230601	MGI			
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0000505	decreased digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15542509
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683376
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0001422	abnormal drinking behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183660
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158594
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15776109
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8521478
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158594
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556900
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11052981
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10987272
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17110378
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10987272
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8521478
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8521478
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14630706
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002679	abnormal corpus luteum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751758
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556900
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751758
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944235
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158594
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732282
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0003177	allodynia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556900
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556900
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183660
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833324
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:8521478
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056763
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11705824
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230601	MGI			
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11052981
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883230
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12118094
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683376
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0005186	increased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751758
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0005527	increased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883230
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0005531	increased renal vascular resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883230
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:15776109
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699263
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008004	abnormal stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:15542509
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:10987272
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683376
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20061361
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:11832369
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008800	increased small intestinal crypt cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11052981
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11282894
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15542509
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699263
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056763
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20230601	MGI			
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20200917	MGI			PMID:15776109
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20200917	MGI			PMID:8521478
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883230
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683376
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009814	increased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11444591
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10683376
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10987272
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11052981
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11705824
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14630706
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699263
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204198
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17219415
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8521478
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751758
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0009818	abnormal thromboxane level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16614756
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751758
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0011021	abnormal circadian regulation of heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883230
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0011022	abnormal circadian regulation of systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883230
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158594
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944235
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732282
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158594
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944235
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0011564	decreased urine prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883230
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0011564	decreased urine prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16614756
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0012008	delayed parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944235
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0012008	delayed parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158594
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0012008	delayed parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:18833324
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0012008	delayed parturition		IAGP		N	RGD:5509061	20191219	MGI			PMID:9751758
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0012009	early parturition		IAGP		N	RGD:5509061	20191219	MGI			PMID:18833324
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0012124	increased bronchoconstrictive response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18753249
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:15776109
11184	Ptgs1	prostaglandin-endoperoxide synthase 1	gene	MP:0031180	decreased brain blood flow rate		IAGP		N	RGD:5509061	20201119	MGI			PMID:11282894
11186	Pth	parathyroid hormone	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
11186	Pth	parathyroid hormone	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20201022	MGI			
11186	Pth	parathyroid hormone	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
11186	Pth	parathyroid hormone	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0003112	enlarged parathyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0004670	small vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0030441	increased osteoblast apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:11994406
11186	Pth	parathyroid hormone	gene	MP:0030479	increased osteocyte apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138191
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:11760831
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792564
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11760831
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138191
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000168	abnormal bone marrow development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20170105	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20141003	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11760831
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11760831
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000447	flattened snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11760831
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20180830	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20180830	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001562	abnormal circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8938591
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20180830	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16355280
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003112	enlarged parathyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003416	premature bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003417	premature endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003417	premature endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16355280
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8938591
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004357	long tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16355280
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004673	splayed ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004950	abnormal brain vasculature morphology		IEA		N	RGD:5509061	20180830	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597768
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138191
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138191
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11760831
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138191
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138191
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11760831
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597768
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597768
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20180830	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0006213	shallow orbits		IAGP		N	RGD:5509061	20171019	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597768
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138191
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138191
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0008922	abnormal cervical rib		IEA		N	RGD:5509061	20180830	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597768
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:11760831
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0010817	absent type I pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0010827	small lung saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11316774
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14751559
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314082
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011145	abnormal mesenchymal cell differentiation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15162506
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597768
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20180830	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0014018	embryo tumor		IEA		N	RGD:5509061	20180830	MGI			
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:19091948
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:15951842
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0030082	long lower incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0030262	frontal bossing		IAGP		N	RGD:5509061	20171026	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0030441	increased osteoblast apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0030449	tooth ankylosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0030453	abnormal odontoblast morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:9391087
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0030479	increased osteocyte apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:11994406
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0030495	absent tooth root		IAGP		N	RGD:5509061	20191219	MGI			PMID:9751753
11188	Pthlh	parathyroid hormone-like peptide	gene	MP:0030505	tooth impaction		IAGP		N	RGD:5509061	20191219	MGI			PMID:9751753
11190	Ptn	pleiotrophin	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001140	abnormal vagina epithelium morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001142	abnormal vagina orifice morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001143	constricted vagina orifice		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482347
11190	Ptn	pleiotrophin	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16619002
11190	Ptn	pleiotrophin	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16619002
11190	Ptn	pleiotrophin	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11414790
11190	Ptn	pleiotrophin	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11414790
11190	Ptn	pleiotrophin	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482347
11190	Ptn	pleiotrophin	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482347
11190	Ptn	pleiotrophin	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482347
11190	Ptn	pleiotrophin	gene	MP:0004895	vagina atrophy		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482347
11190	Ptn	pleiotrophin	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0009014	prolonged proestrus		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0009018	short estrus		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0009708	vaginal septum		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220120	MGI			PMID:17121547
11190	Ptn	pleiotrophin	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:17121547
11192	Ptprg	protein tyrosine phosphatase receptor type G	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029056
11192	Ptprg	protein tyrosine phosphatase receptor type G	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782895
11192	Ptprg	protein tyrosine phosphatase receptor type G	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782895
11192	Ptprg	protein tyrosine phosphatase receptor type G	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782895
11192	Ptprg	protein tyrosine phosphatase receptor type G	gene	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782895
11192	Ptprg	protein tyrosine phosphatase receptor type G	gene	MP:0002738	hyperresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782895
11192	Ptprg	protein tyrosine phosphatase receptor type G	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029056
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932834
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932834
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932834
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0002068	abnormal parental behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10339427
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10339427
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932834
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10339427
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20210429	MGI			PMID:32491951
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10339427
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20201022	MGI			
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18046458
11194	Ptpra	protein tyrosine phosphatase receptor type A	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779349
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20151119	MGI			PMID:22724066
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10970857
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:24068938
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15823427
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15823427
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779349
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001664	abnormal digestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20151203	MGI			PMID:24068938
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001800	abnormal humoral immune response		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346773
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346773
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10970857
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346773
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22988576
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9725213
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779349
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20190418	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002619	abnormal lymphocyte morphology		IEA		N	RGD:5509061	20190411	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867094
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0004917	abnormal T cell selection		IEA		N	RGD:5509061	20111116	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779349
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IEA		N	RGD:5509061	20190418	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20151119	MGI			PMID:22724066
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20151119	MGI			PMID:22724066
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9725213
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20151203	MGI			PMID:24068938
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346773
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8046327
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20151203	MGI			PMID:24068938
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IEA		N	RGD:5509061	20190411	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9725213
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008037	abnormal T cell morphology		IEA		N	RGD:5509061	20111116	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20190103	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867094
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20190411	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008048	abnormal memory T cell number		IEA		N	RGD:5509061	20111116	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008050	decreased memory T cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008070	absent T cells		IEA		N	RGD:5509061	20111116	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346773
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20151203	MGI			PMID:24068938
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8334701
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666928
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20151203	MGI			PMID:24068938
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008082	increased single-positive T cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008126	increased dendritic cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008170	decreased B-1b cell number		IEA		N	RGD:5509061	20181011	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008172	abnormal follicular B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008188	abnormal transitional stage B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008191	abnormal follicular B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19299707
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008246	abnormal leukocyte morphology		IEA		N	RGD:5509061	20111116	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9725213
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008400	abnormal CD4-positive, alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9725213
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867094
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008729	decreased memory B cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20180329	MGI			PMID:29440507
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8046327
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008894	abnormal intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9725213
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0008895	abnormal intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9725213
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0009785	abnormal susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180329	MGI			PMID:29440507
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15823427
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20151203	MGI			PMID:24068938
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20151203	MGI			PMID:24068938
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867094
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16627620
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20180329	MGI			PMID:29440507
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010836	decreased CD4-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010839	decreased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20150129	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181004	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181004	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190613	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181004	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010848	decreased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190613	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181004	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508267
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20181004	MGI			
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:18249142
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:11163182
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:24068938
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:29440507
11196	Ptprc	protein tyrosine phosphatase receptor type C	gene	MP:0031045	decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:29440507
11199	Pvalb	parvalbumin	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860487
11199	Pvalb	parvalbumin	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15836427
11199	Pvalb	parvalbumin	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:25116249
11199	Pvalb	parvalbumin	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20160304	MGI			PMID:26590342
11199	Pvalb	parvalbumin	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20150122	MGI			PMID:24430185
11199	Pvalb	parvalbumin	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160304	MGI			PMID:26590342
11199	Pvalb	parvalbumin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20150917	MGI			PMID:24995986
11199	Pvalb	parvalbumin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160304	MGI			PMID:26590342
11199	Pvalb	parvalbumin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160407	MGI			PMID:25116249
11199	Pvalb	parvalbumin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160304	MGI			PMID:26590342
11199	Pvalb	parvalbumin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
11199	Pvalb	parvalbumin	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20160304	MGI			PMID:26590342
11199	Pvalb	parvalbumin	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20150122	MGI			PMID:24430185
11199	Pvalb	parvalbumin	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
11199	Pvalb	parvalbumin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160304	MGI			PMID:26590342
11199	Pvalb	parvalbumin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
11199	Pvalb	parvalbumin	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023653
11199	Pvalb	parvalbumin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20231123	MGI			PMID:27618674
11199	Pvalb	parvalbumin	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20150122	MGI			PMID:24430185
11199	Pvalb	parvalbumin	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24430185
11199	Pvalb	parvalbumin	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
11199	Pvalb	parvalbumin	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378872
11199	Pvalb	parvalbumin	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0004167	abnormal cingulate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23671099
11199	Pvalb	parvalbumin	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20190620	MGI			PMID:27253061
11199	Pvalb	parvalbumin	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
11199	Pvalb	parvalbumin	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0005583	decreased renin activity		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950767
11199	Pvalb	parvalbumin	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860487
11199	Pvalb	parvalbumin	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378872
11199	Pvalb	parvalbumin	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20160304	MGI			PMID:26590342
11199	Pvalb	parvalbumin	gene	MP:0012306	enhanced spatial learning		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0012318	slow extinction of fear memory		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0012339	hyperkalemia		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20200604	MGI			PMID:28442491
11199	Pvalb	parvalbumin	gene	MP:0014331	abnormal Purkinje cell mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:16860487
11199	Pvalb	parvalbumin	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20170105	MGI			PMID:27131348
11199	Pvalb	parvalbumin	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22378872
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20170629	MGI			PMID:27736879
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170629	MGI			PMID:27736879
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20170629	MGI			PMID:27736879
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20170629	MGI			PMID:27736879
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20170629	MGI			PMID:27736879
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0010158	abnormal intestine development		IAGP		N	RGD:5509061	20170629	MGI			PMID:27736879
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20231207	MGI			
11204	Slc39a7	solute carrier family 39 (zinc transporter), member 7	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20170629	MGI			PMID:27736879
11205	H2-M3	histocompatibility 2, M region locus 3	gene	MP:0001830	decreased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476767
11205	H2-M3	histocompatibility 2, M region locus 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476767
11205	H2-M3	histocompatibility 2, M region locus 3	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476767
11205	H2-M3	histocompatibility 2, M region locus 3	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476767
11205	H2-M3	histocompatibility 2, M region locus 3	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476767
11205	H2-M3	histocompatibility 2, M region locus 3	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476767
11205	H2-M3	histocompatibility 2, M region locus 3	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476767
11205	H2-M3	histocompatibility 2, M region locus 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
11205	H2-M3	histocompatibility 2, M region locus 3	gene	MP:0011077	decreased macrophage nitric oxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476767
11210	Art2a	ADP-ribosyltransferase 2a	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9300695
11210	Art2a	ADP-ribosyltransferase 2a	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585549
11210	Art2a	ADP-ribosyltransferase 2a	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585549
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436611
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436611
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0002916	increased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:7911226
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436611
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269275
11212	Rab3a	RAB3A, member RAS oncogene family	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:12244319
11213	Rab4a	RAB4A, member RAS oncogene family	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
11213	Rab4a	RAB4A, member RAS oncogene family	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
11213	Rab4a	RAB4A, member RAS oncogene family	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
11213	Rab4a	RAB4A, member RAS oncogene family	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467832
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18922468
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514245
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000447	flattened snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17396120
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17396120
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20170105	MGI			
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20170105	MGI			
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17396120
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514245
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296227
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17396120
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514245
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17396120
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467832
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467832
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467832
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467832
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:17396120
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003820	increased left ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18922468
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15467832
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11157055
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16527894
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0006207	embryonic lethality during organogenesis		IEA		N	RGD:5509061	20111116	MGI			
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008526	decreased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008727	increased heart right atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18922468
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453624
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0010031	abnormal cranium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0010283	decreased classified tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514245
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0010583	abnormal conotruncus morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0010754	abnormal heart left ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17396120
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16432225
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17396120
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18922468
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339642
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826437
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0012099	decreased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0012244	increased hepatoblast apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:11296228
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:18922468
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:16527894
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:9767153
11215	Raf1	Raf1 proto-oncogene, serine/threonine kinase	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15467832
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000044	absent organ of Corti		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000075	absent neurocranium		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000099	absent vomer bone		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0000935	abnormal folding of telencephalic vesicles		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001070	abnormal abducens nerve morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857786
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001310	abnormal conjunctiva morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857786
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901285
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901285
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7679509
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002257	abnormal arytenoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002257	abnormal arytenoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002265	abnormal left major bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002266	abnormal right major bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20150122	MGI			PMID:24458645
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901285
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003146	absent cochlear ganglion		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003557	absent vas deferens		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003558	absent uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003558	absent uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003575	absent oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003575	absent oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003600	ectopic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18026104
11216	Rara	retinoic acid receptor, alpha	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004550	short trachea		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004553	absent tracheal cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004666	absent stapedial artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004666	absent stapedial artery		IAGP		N	RGD:5509061	20170921	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901285
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0005623	abnormal meninges morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0006289	otic capsule hypoplasia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901285
11216	Rara	retinoic acid receptor, alpha	gene	MP:0006425	absent Mullerian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0006425	absent Mullerian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901285
11216	Rara	retinoic acid receptor, alpha	gene	MP:0008380	abnormal gonial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0008823	abnormal interventricular septum membranous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0008881	absent Harderian gland		IAGP		N	RGD:5509061	20150205	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0008881	absent Harderian gland		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009054	absent anal canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009054	absent anal canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009072	absent cranial vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009072	absent cranial vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009075	rudimentary Wolffian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009076	rudimentary Mullerian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009438	cricoid and tracheal cartilage fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009525	abnormal submandibular duct morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009526	absent sublingual gland		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009527	abnormal sublingual duct morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009569	abnormal left lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009570	abnormal right lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0009571	abnormal right lung accessory lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010502	ventricle myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010565	absent fetal ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010572	persistent right dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010584	abnormal conotruncus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010595	abnormal aortic valve cusp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010702	split cervical atlas		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010703	split cervical axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010709	absent eye anterior chamber		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010712	absent nasolacrimal duct		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010713	corneal-lenticular stalk		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010715	retina coloboma		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010717	optic nerve coloboma		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010720	absent sublingual duct		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010721	short sublingual duct		IAGP		N	RGD:5509061	20171207	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010721	short sublingual duct		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010722	persistent cervical thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010722	persistent cervical thymus		IAGP		N	RGD:5509061	20171207	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010772	abnormal pollex morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010980	ectopic ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010987	abnormal nephrogenic mesenchyme morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11216	Rara	retinoic acid receptor, alpha	gene	MP:0010989	fused bronchial cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8394014
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011306	absent kidney pelvis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011407	absent nephrogenic zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011486	ectopic ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0011486	ectopic ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0012141	absent hindbrain		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0012247	absent cornea		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0012523	abnormal upper lip morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0013233	ectopic thyroid gland		IAGP		N	RGD:5509061	20150122	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0013331	abnormal lacrimal gland development		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0013439	abnormal Harderian gland development		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20150305	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0013744	abnormal conjunctival sac morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0013826	absent hypoglossal canal		IAGP		N	RGD:5509061	20171026	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0030200	abnormal nasal septum cartilage morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0030304	abnormal cribriform plate morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0030394	abnormal incus short process morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11216	Rara	retinoic acid receptor, alpha	gene	MP:0030406	absent stapes obturator foramen		IAGP		N	RGD:5509061	20171207	MGI			PMID:9240560
11216	Rara	retinoic acid receptor, alpha	gene	MP:0030416	absent temporal bone zygomatic process		IAGP		N	RGD:5509061	20171214	MGI			PMID:9376317
11216	Rara	retinoic acid receptor, alpha	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:7607068
11216	Rara	retinoic acid receptor, alpha	gene	MP:0031445	midline cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074013
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635054
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635054
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20241121	MGI			
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20241121	MGI			
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883728
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883728
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883728
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958449
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002257	abnormal arytenoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002265	abnormal left major bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002266	abnormal right major bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002271	abnormal pulmonary alveolar duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635054
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635054
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883728
11217	Rarb	retinoic acid receptor, beta	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003182	decreased pulmonary endothelial cell surface		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635054
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003558	absent uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003558	absent uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003575	absent oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003575	absent oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003600	ectopic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004666	absent stapedial artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005208	abnormal iris stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635054
11217	Rarb	retinoic acid receptor, beta	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0006200	vitreous body deposition		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0006425	absent Mullerian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0006425	absent Mullerian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0008380	abnormal gonial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0008514	absent retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0008823	abnormal interventricular septum membranous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0008881	absent Harderian gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0008972	ethmoturbinate hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009054	absent anal canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009054	absent anal canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009072	absent cranial vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009072	absent cranial vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009076	rudimentary Mullerian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009438	cricoid and tracheal cartilage fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009438	cricoid and tracheal cartilage fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009569	abnormal left lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009570	abnormal right lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0009571	abnormal right lung accessory lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20241121	MGI			
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010565	absent fetal ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010572	persistent right dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010584	abnormal conotruncus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010595	abnormal aortic valve cusp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010702	split cervical atlas		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010703	split cervical axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010705	absent metoptic pillar		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010706	ventral rotation of lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010706	ventral rotation of lens		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010707	decreased ventral retina size		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010709	absent eye anterior chamber		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010709	absent eye anterior chamber		IAGP		N	RGD:5509061	20201119	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010710	absent sclera		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857787
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010712	absent nasolacrimal duct		IAGP		N	RGD:5509061	20141211	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010712	absent nasolacrimal duct		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010714	iris coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010715	retina coloboma		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010716	optic disk coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010717	optic nerve coloboma		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010721	short sublingual duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010721	short sublingual duct		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010722	persistent cervical thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010722	persistent cervical thymus		IAGP		N	RGD:5509061	20171207	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635054
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010902	abnormal pulmonary alveolar sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074013
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010902	abnormal pulmonary alveolar sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15635054
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010980	ectopic ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010987	abnormal nephrogenic mesenchyme morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010989	fused bronchial cartilage rings		IAGP		N	RGD:5509061	20150212	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0010995	abnormal lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11074013
11217	Rarb	retinoic acid receptor, beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021334
11217	Rarb	retinoic acid receptor, beta	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0011407	absent nephrogenic zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0011486	ectopic ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0011486	ectopic ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0013331	abnormal lacrimal gland development		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0013439	abnormal Harderian gland development		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20150305	MGI			PMID:7607068
11217	Rarb	retinoic acid receptor, beta	gene	MP:0013744	abnormal conjunctival sac morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0013744	abnormal conjunctival sac morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
11217	Rarb	retinoic acid receptor, beta	gene	MP:0013744	abnormal conjunctival sac morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0013826	absent hypoglossal canal		IAGP		N	RGD:5509061	20171026	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:9240560
11217	Rarb	retinoic acid receptor, beta	gene	MP:0030326	decreased periocular mesenchyme apoptosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:16207763
11217	Rarb	retinoic acid receptor, beta	gene	MP:0030394	abnormal incus short process morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11217	Rarb	retinoic acid receptor, beta	gene	MP:0030406	absent stapes obturator foramen		IAGP		N	RGD:5509061	20171207	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000044	absent organ of Corti		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000075	absent neurocranium		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559481
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000099	absent vomer bone		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0000935	abnormal folding of telencephalic vesicles		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001070	abnormal abducens nerve morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7631783
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559481
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001310	abnormal conjunctiva morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7631783
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559481
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857788
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7631783
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002257	abnormal arytenoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559481
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003146	absent cochlear ganglion		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003557	absent vas deferens		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003558	absent uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003639	abnormal response to vitamins		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004550	short trachea		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004552	fused tracheal cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:7631783
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004552	fused tracheal cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004552	fused tracheal cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004553	absent tracheal cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004658	abnormal ventral tubercle of atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004666	absent stapedial artery		IAGP		N	RGD:5509061	20170921	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005208	abnormal iris stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005248	abnormal Harderian gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7631783
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005248	abnormal Harderian gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0005623	abnormal meninges morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0006289	otic capsule hypoplasia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0008514	absent retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0008823	abnormal interventricular septum membranous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:7631783
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0008881	absent Harderian gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0008881	absent Harderian gland		IAGP		N	RGD:5509061	20150205	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0008881	absent Harderian gland		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0008972	ethmoturbinate hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009072	absent cranial vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009075	rudimentary Wolffian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009076	rudimentary Mullerian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009438	cricoid and tracheal cartilage fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009438	cricoid and tracheal cartilage fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009525	abnormal submandibular duct morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009526	absent sublingual gland		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009527	abnormal sublingual duct morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0009608	abnormal epidermal lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010502	ventricle myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010565	absent fetal ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010572	persistent right dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010702	split cervical atlas		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010703	split cervical axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010705	absent metoptic pillar		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010706	ventral rotation of lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010706	ventral rotation of lens		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010707	decreased ventral retina size		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010709	absent eye anterior chamber		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010709	absent eye anterior chamber		IAGP		N	RGD:5509061	20201119	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010710	absent sclera		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010712	absent nasolacrimal duct		IAGP		N	RGD:5509061	20141211	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010712	absent nasolacrimal duct		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010713	corneal-lenticular stalk		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010714	iris coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010715	retina coloboma		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010716	optic disk coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010717	optic nerve coloboma		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010720	absent sublingual duct		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010721	short sublingual duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010721	short sublingual duct		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010722	persistent cervical thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559481
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010772	abnormal pollex morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0010989	fused bronchial cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0011306	absent kidney pelvis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0011486	ectopic ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0012141	absent hindbrain		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0012247	absent cornea		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0012523	abnormal upper lip morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013233	ectopic thyroid gland		IAGP		N	RGD:5509061	20150122	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013319	seminal vesicle atrophy		IAGP		N	RGD:5509061	20141204	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013321	squamous metaplasia of seminal vesicles		IAGP		N	RGD:5509061	20141204	MGI			PMID:11857788
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013321	squamous metaplasia of seminal vesicles		IAGP		N	RGD:5509061	20141204	MGI			PMID:7631783
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013321	squamous metaplasia of seminal vesicles		IAGP		N	RGD:5509061	20141204	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013322	squamous metaplasia of prostate gland		IAGP		N	RGD:5509061	20141204	MGI			PMID:11857788
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013322	squamous metaplasia of prostate gland		IAGP		N	RGD:5509061	20141204	MGI			PMID:7631783
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013322	squamous metaplasia of prostate gland		IAGP		N	RGD:5509061	20141204	MGI			PMID:8388780
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013331	abnormal lacrimal gland development		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013439	abnormal Harderian gland development		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20150305	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013744	abnormal conjunctival sac morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013744	abnormal conjunctival sac morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0013744	abnormal conjunctival sac morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:9240560
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0030200	abnormal nasal septum cartilage morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0030304	abnormal cribriform plate morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0030326	decreased periocular mesenchyme apoptosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:16207763
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0030394	abnormal incus short process morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:7607067
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0030416	absent temporal bone zygomatic process		IAGP		N	RGD:5509061	20171214	MGI			PMID:9376317
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:7607068
11218	Rarg	retinoic acid receptor, gamma	gene	MP:0031445	midline cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:7607067
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653467
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925271
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925271
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925270
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19506017
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000631	abnormal neuroendocrine gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8134105
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9537419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000798	abnormal frontal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000829	dilated fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925270
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925270
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22611036
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103190
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103190
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103190
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:8134105
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12839925
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23486187
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:8134105
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20220519	MGI			PMID:34099734
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925270
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001492	abnormal pilomotor reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12360286
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23079656
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001885	mammary gland duct hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19506017
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001885	mammary gland duct hyperplasia		IAGP		N	RGD:5509061	20150212	MGI			PMID:24662053
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20150212	MGI			PMID:24662053
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653467
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002009	preneoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925270
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574128
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12096340
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16029419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176372
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9537419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19765830
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002031	increased adrenal gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574128
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9214616
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925270
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8134105
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671308
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002050	increased pheochromocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002050	increased pheochromocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653467
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20406986
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574128
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22611036
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23486187
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9537419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671308
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160512	MGI			PMID:17637742
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20161013	MGI			PMID:26659571
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220519	MGI			PMID:34099734
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230601	MGI			PMID:30093633
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20027616
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671308
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925271
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925271
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16029419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9537419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23486187
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003315	abnormal perineum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21573126
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21875955
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003365	increased glucagonoma incidence		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12096340
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:35700263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003496	increased thyroid adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9537419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12839925
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:19506017
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612004
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20230601	MGI			PMID:30093633
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003745	abnormal oral mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176372
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23486187
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20161013	MGI			PMID:26659571
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:29743593
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:30093633
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:35700263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:36073547
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003838	abnormal milk ejection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19506017
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612004
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21573126
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612004
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004327	increased vestibular hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653467
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004327	increased vestibular hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653467
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653467
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004407	increased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653467
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004407	increased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004478	increased testicular teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004498	increased organ of Corti supporting cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004840	increased Deiters cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653467
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004898	uterine hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9537419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15353549
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23079656
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23079656
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925270
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8134105
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20160915	MGI			PMID:25252918
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12360286
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005299	abnormal eye posterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005488	bronchial epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843406
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12360286
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12360286
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:12584165
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006096	absent retina bipolar cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006096	absent retina bipolar cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925270
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:12810584
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574128
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006310	increased retinoblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006310	increased retinoblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0006310	increased retinoblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12839925
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19765830
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20406986
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21573126
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008068	absent retina ganglion cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008113	abnormal macrophage differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008130	abnormal pituitary intermediate lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671308
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008301	adrenal medulla hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9537419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008306	abnormal organ of Corti supporting cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653467
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008306	abnormal organ of Corti supporting cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008371	pituitary intermediate lobe hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671308
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008512	disorganized retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008534	enlarged fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19765830
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20406986
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22611036
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008796	increased lens fiber apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20150212	MGI			PMID:24662053
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20220519	MGI			PMID:34099734
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009320	increased lymphoblastic lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009408	decreased skeletal muscle fiber density		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20150212	MGI			PMID:24662053
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:25252918
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12360286
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12360286
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670909
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010281	increased nervous system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23887970
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20230601	MGI			PMID:30093633
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20230601	MGI			PMID:36073547
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574128
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9537419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20150212	MGI			PMID:24662053
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20160512	MGI			PMID:17637742
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010321	increased parathyroid gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010344	increased hibernoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23486187
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010345	increased thyroid C-cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010345	increased thyroid C-cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010346	increased thyroid carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19765830
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010346	increased thyroid carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010348	increased pancreatic islet cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010348	increased pancreatic islet cell carcinoma incidence		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010350	increased pituitary adenohypophysis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12096340
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010350	increased pituitary adenohypophysis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010350	increased pituitary adenohypophysis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010351	increased pituitary melanotroph tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12096340
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010351	increased pituitary melanotroph tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010351	increased pituitary melanotroph tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893233
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010351	increased pituitary melanotroph tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7925271
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010351	increased pituitary melanotroph tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20220519	MGI			PMID:34099734
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0010918	abnormal pulmonary neuroendocrine body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16029419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150212	MGI			PMID:24662053
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529408
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150212	MGI			PMID:24662053
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9537419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12096340
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406932
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12360286
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16029419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0011804	increased cell migration		IAGP		N	RGD:5509061	20161013	MGI			PMID:26659571
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200409	MGI			PMID:27889452
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:29743593
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:35700263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:12839925
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:16029419
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21573126
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:24292676
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:27889452
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:29743593
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:35700263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:8682293
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:9671308
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014754	abnormal tumor progression		IAGP		N	RGD:5509061	20250904	MGI			PMID:33594717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:33594717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:33594717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:1406933
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260507	MGI			PMID:16449662
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:8957005
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0015067	increased myocardial fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:15743840
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0021056	abnormal tumor vascular morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:35700263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:15231717
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:17235288
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0030006	decreased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:12360286
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0030047	flat forehead		IAGP		N	RGD:5509061	20170921	MGI			PMID:1406937
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0031278	decreased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:29743593
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0031278	decreased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:35700263
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0031278	decreased osteosarcoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11219	Rb1	RB transcriptional corepressor 1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000397	abnormal guard hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20406986
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002683	delayed fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21875955
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20171102	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20160915	MGI			PMID:25252918
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0006096	absent retina bipolar cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0006310	increased retinoblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0006310	increased retinoblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0006399	abnormal long bone epiphyseal ossification zone morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151761
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20406986
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0008068	absent retina ganglion cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0008161	increased diameter of radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0008163	increased diameter of ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0008218	delayed emergence of vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20406986
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:25252918
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0013168	absent hindlimb buds		IAGP		N	RGD:5509061	20150528	MGI			PMID:9806916
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:15231717
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:8682294
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0015067	increased myocardial fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:15743840
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:17235288
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0030079	small incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:12702649
11220	Rbl2	RB transcriptional corepressor like 2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15743840
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11222375
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11222375
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0003011	delayed dark adaptation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036972
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0005444	abnormal retinol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0011234	abnormal retinol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487743
11221	Rbp1	retinol binding protein 1, cellular	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
11226	Rbp2	retinol binding protein 2, cellular	gene	MP:0001671	abnormal vitamin absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12138113
11226	Rbp2	retinol binding protein 2, cellular	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12138113
11226	Rbp2	retinol binding protein 2, cellular	gene	MP:0011234	abnormal retinol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12138113
11227	Rbp3	retinol binding protein 3, interstitial	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9614228
11227	Rbp3	retinol binding protein 3, interstitial	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9614228
11227	Rbp3	retinol binding protein 3, interstitial	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508404
11227	Rbp3	retinol binding protein 3, interstitial	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9614228
11227	Rbp3	retinol binding protein 3, interstitial	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9614228
11227	Rbp3	retinol binding protein 3, interstitial	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9614228
11234	Ret	ret proto-oncogene	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565500
11234	Ret	ret proto-oncogene	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414682
11234	Ret	ret proto-oncogene	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050626
11234	Ret	ret proto-oncogene	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565500
11234	Ret	ret proto-oncogene	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565500
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065462
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372903
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414682
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216204
11234	Ret	ret proto-oncogene	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565500
11234	Ret	ret proto-oncogene	gene	MP:0000576	clubfoot		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600854
11234	Ret	ret proto-oncogene	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372903
11234	Ret	ret proto-oncogene	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0000909	abnormal facial motor nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216204
11234	Ret	ret proto-oncogene	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
11234	Ret	ret proto-oncogene	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
11234	Ret	ret proto-oncogene	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0001014	absent superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565847
11234	Ret	ret proto-oncogene	gene	MP:0001015	small superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0001017	abnormal stellate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565847
11234	Ret	ret proto-oncogene	gene	MP:0001025	abnormal sympathetic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414682
11234	Ret	ret proto-oncogene	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565500
11234	Ret	ret proto-oncogene	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050626
11234	Ret	ret proto-oncogene	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372903
11234	Ret	ret proto-oncogene	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414682
11234	Ret	ret proto-oncogene	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
11234	Ret	ret proto-oncogene	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565500
11234	Ret	ret proto-oncogene	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050626
11234	Ret	ret proto-oncogene	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065462
11234	Ret	ret proto-oncogene	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565500
11234	Ret	ret proto-oncogene	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050626
11234	Ret	ret proto-oncogene	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065462
11234	Ret	ret proto-oncogene	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565847
11234	Ret	ret proto-oncogene	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600854
11234	Ret	ret proto-oncogene	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216204
11234	Ret	ret proto-oncogene	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065462
11234	Ret	ret proto-oncogene	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20180517	MGI			PMID:29192291
11234	Ret	ret proto-oncogene	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20180920	MGI			PMID:29321660
11234	Ret	ret proto-oncogene	gene	MP:0002050	increased pheochromocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0002050	increased pheochromocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321127
11234	Ret	ret proto-oncogene	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180920	MGI			PMID:29321660
11234	Ret	ret proto-oncogene	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541311
11234	Ret	ret proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216204
11234	Ret	ret proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20064391
11234	Ret	ret proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
11234	Ret	ret proto-oncogene	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242795
11234	Ret	ret proto-oncogene	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
11234	Ret	ret proto-oncogene	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19755105
11234	Ret	ret proto-oncogene	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414682
11234	Ret	ret proto-oncogene	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600854
11234	Ret	ret proto-oncogene	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
11234	Ret	ret proto-oncogene	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
11234	Ret	ret proto-oncogene	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414682
11234	Ret	ret proto-oncogene	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11234	Ret	ret proto-oncogene	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
11234	Ret	ret proto-oncogene	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0003358	abnormal hypaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
11234	Ret	ret proto-oncogene	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
11234	Ret	ret proto-oncogene	gene	MP:0003496	increased thyroid adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372903
11234	Ret	ret proto-oncogene	gene	MP:0003498	thyroid gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0003585	large ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0003587	ureter obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0003588	ureter stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0003600	ectopic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
11234	Ret	ret proto-oncogene	gene	MP:0003613	abnormal kidney medulla development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0003685	abnormal cardiac ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10974669
11234	Ret	ret proto-oncogene	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
11234	Ret	ret proto-oncogene	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305247
11234	Ret	ret proto-oncogene	gene	MP:0004281	abnormal hypoglossal nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216204
11234	Ret	ret proto-oncogene	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
11234	Ret	ret proto-oncogene	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
11234	Ret	ret proto-oncogene	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
11234	Ret	ret proto-oncogene	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141016	MGI			PMID:24780737
11234	Ret	ret proto-oncogene	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668632
11234	Ret	ret proto-oncogene	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050626
11234	Ret	ret proto-oncogene	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0008289	abnormal adrenal medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0008298	adrenergic chromaffin cell hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0008299	adrenal cortical hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372903
11234	Ret	ret proto-oncogene	gene	MP:0008312	abnormal sympathetic postganglionic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0008313	abnormal parasympathetic postganglionic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10974669
11234	Ret	ret proto-oncogene	gene	MP:0008314	abnormal pterygopalatine ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0008316	abnormal prevertebral ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0008487	abnormal mesonephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674430
11234	Ret	ret proto-oncogene	gene	MP:0009483	enlarged ileum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0009485	distended ileum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0009843	decreased neural crest cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414682
11234	Ret	ret proto-oncogene	gene	MP:0009857	absent kidney cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372903
11234	Ret	ret proto-oncogene	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11234	Ret	ret proto-oncogene	gene	MP:0010362	increased ganglioneuroma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0010980	ectopic ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0010981	abnormal branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674430
11234	Ret	ret proto-oncogene	gene	MP:0010982	abnormal ureteric bud elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674430
11234	Ret	ret proto-oncogene	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674430
11234	Ret	ret proto-oncogene	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674430
11234	Ret	ret proto-oncogene	gene	MP:0010985	abnormal kidney mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340065
11234	Ret	ret proto-oncogene	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
11234	Ret	ret proto-oncogene	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675330
11234	Ret	ret proto-oncogene	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641220
11234	Ret	ret proto-oncogene	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565500
11234	Ret	ret proto-oncogene	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372903
11234	Ret	ret proto-oncogene	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216204
11234	Ret	ret proto-oncogene	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
11234	Ret	ret proto-oncogene	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674430
11234	Ret	ret proto-oncogene	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469971
11234	Ret	ret proto-oncogene	gene	MP:0011407	absent nephrogenic zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0011407	absent nephrogenic zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0011410	ectopic testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0011438	absent kidney medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0011727	ectopic ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452504
11234	Ret	ret proto-oncogene	gene	MP:0011797	blind ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0011797	blind ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:8114940
11234	Ret	ret proto-oncogene	gene	MP:0012171	oligohydramnios		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595168
11234	Ret	ret proto-oncogene	gene	MP:0013001	abnormal enteric neural crest cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050626
11234	Ret	ret proto-oncogene	gene	MP:0013003	absent enteric neural crest cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0013003	absent enteric neural crest cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227613
11234	Ret	ret proto-oncogene	gene	MP:0013006	abnormal enteric neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562352
11234	Ret	ret proto-oncogene	gene	MP:0013006	abnormal enteric neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050626
11234	Ret	ret proto-oncogene	gene	MP:0013006	abnormal enteric neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414682
11234	Ret	ret proto-oncogene	gene	MP:0013006	abnormal enteric neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392943
11234	Ret	ret proto-oncogene	gene	MP:0013006	abnormal enteric neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565847
11234	Ret	ret proto-oncogene	gene	MP:0014484	decreased feces water content		IAGP		N	RGD:5509061	20240704	MGI			PMID:20392943
11237	Rgn	regucalcin	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733551
11237	Rgn	regucalcin	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482009
11237	Rgn	regucalcin	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975739
11237	Rgn	regucalcin	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482009
11237	Rgn	regucalcin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975739
11237	Rgn	regucalcin	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728709
11237	Rgn	regucalcin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728709
11237	Rgn	regucalcin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975739
11237	Rgn	regucalcin	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16500693
11237	Rgn	regucalcin	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975739
11237	Rgn	regucalcin	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482009
11237	Rgn	regucalcin	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733551
11237	Rgn	regucalcin	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16500693
11237	Rgn	regucalcin	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728709
11237	Rgn	regucalcin	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368201
11237	Rgn	regucalcin	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975739
11237	Rgn	regucalcin	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728709
11237	Rgn	regucalcin	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975739
11237	Rgn	regucalcin	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975739
11237	Rgn	regucalcin	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975739
11237	Rgn	regucalcin	gene	MP:0010252	anterior subcapsular cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155581
11237	Rgn	regucalcin	gene	MP:0010911	abnormal pulmonary acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14989739
11237	Rgn	regucalcin	gene	MP:0010911	abnormal pulmonary acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728709
11237	Rgn	regucalcin	gene	MP:0011229	abnormal vitamin C level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0011229	abnormal vitamin C level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482009
11237	Rgn	regucalcin	gene	MP:0011229	abnormal vitamin C level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733551
11237	Rgn	regucalcin	gene	MP:0011229	abnormal vitamin C level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155581
11237	Rgn	regucalcin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733551
11237	Rgn	regucalcin	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:14975739
11237	Rgn	regucalcin	gene	MP:0014867	increased malondialdehyde level		IAGP		N	RGD:5509061	20260212	MGI			PMID:16728709
11237	Rgn	regucalcin	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0030679	decreased hydroxyproline level		IAGP		N	RGD:5509061	20180920	MGI			PMID:19482009
11237	Rgn	regucalcin	gene	MP:0030827	femur fracture		IAGP		N	RGD:5509061	20181101	MGI			PMID:16585534
11237	Rgn	regucalcin	gene	MP:0030884	rachitic rosary		IAGP		N	RGD:5509061	20181101	MGI			PMID:16585534
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593615
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21357625
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593615
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593615
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593615
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593615
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593615
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593615
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593615
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:21357625
11238	Rgs16	regulator of G-protein signaling 16	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:21610730
11239	Rho	rhodopsin	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979686
11239	Rho	rhodopsin	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22252712
11239	Rho	rhodopsin	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020854
11239	Rho	rhodopsin	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161873
11239	Rho	rhodopsin	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892703
11239	Rho	rhodopsin	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22110080
11239	Rho	rhodopsin	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22252712
11239	Rho	rhodopsin	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23940033
11239	Rho	rhodopsin	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15184660
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15851469
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979686
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22110080
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23940033
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20150129	MGI			PMID:21052544
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20191212	MGI			PMID:22809998
11239	Rho	rhodopsin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161873
11239	Rho	rhodopsin	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892703
11239	Rho	rhodopsin	gene	MP:0001999	photosensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892703
11239	Rho	rhodopsin	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0003011	delayed dark adaptation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979686
11239	Rho	rhodopsin	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
11239	Rho	rhodopsin	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979686
11239	Rho	rhodopsin	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15939043
11239	Rho	rhodopsin	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466416
11239	Rho	rhodopsin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723493
11239	Rho	rhodopsin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17194706
11239	Rho	rhodopsin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22110080
11239	Rho	rhodopsin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020854
11239	Rho	rhodopsin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20171207	MGI			PMID:28859131
11239	Rho	rhodopsin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020854
11239	Rho	rhodopsin	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:28859131
11239	Rho	rhodopsin	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466416
11239	Rho	rhodopsin	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161873
11239	Rho	rhodopsin	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723493
11239	Rho	rhodopsin	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161873
11239	Rho	rhodopsin	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161873
11239	Rho	rhodopsin	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161873
11239	Rho	rhodopsin	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466416
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161873
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15939043
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979686
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22110080
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
11239	Rho	rhodopsin	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15851469
11239	Rho	rhodopsin	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15939043
11239	Rho	rhodopsin	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
11239	Rho	rhodopsin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466416
11239	Rho	rhodopsin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15851469
11239	Rho	rhodopsin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979686
11239	Rho	rhodopsin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22252712
11239	Rho	rhodopsin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020854
11239	Rho	rhodopsin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892703
11239	Rho	rhodopsin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
11239	Rho	rhodopsin	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892703
11239	Rho	rhodopsin	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20191212	MGI			PMID:22809998
11239	Rho	rhodopsin	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
11239	Rho	rhodopsin	gene	MP:0008581	disorganized photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
11239	Rho	rhodopsin	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23940033
11239	Rho	rhodopsin	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020854
11239	Rho	rhodopsin	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892703
11239	Rho	rhodopsin	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020854
11239	Rho	rhodopsin	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22252712
11239	Rho	rhodopsin	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9020854
11239	Rho	rhodopsin	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892703
11239	Rho	rhodopsin	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20191212	MGI			PMID:22809998
11239	Rho	rhodopsin	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
11239	Rho	rhodopsin	gene	MP:0011234	abnormal retinol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20171207	MGI			PMID:28859131
11239	Rho	rhodopsin	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0012033	abnormal ERG implicit time		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:22252712
11239	Rho	rhodopsin	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:22252712
11239	Rho	rhodopsin	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:15851469
11239	Rho	rhodopsin	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:21224384
11239	Rho	rhodopsin	gene	MP:0014658	absent a-wave		IAGP		N	RGD:5509061	20250410	MGI			PMID:22809998
11239	Rho	rhodopsin	gene	MP:0020439	absent b-wave		IAGP		N	RGD:5509061	20191212	MGI			PMID:22809998
11239	Rho	rhodopsin	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:19741247
11239	Rho	rhodopsin	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:20207741
11239	Rho	rhodopsin	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:23940033
11239	Rho	rhodopsin	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20250731	MGI			PMID:35275162
11239	Rho	rhodopsin	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:9020854
11239	Rho	rhodopsin	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:9892703
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25910808
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23271052
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19456252
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832488
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19456252
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19456252
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20151112	MGI			PMID:18718479
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25910808
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832488
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832488
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832488
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832488
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25910808
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25910808
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20151112	MGI			PMID:18718479
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20151112	MGI			PMID:18718479
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20160128	MGI			PMID:24135024
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0005260	ocular hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:19456252
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20151112	MGI			PMID:25910808
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0005406	abnormal heart size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23271052
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20160128	MGI			PMID:24135024
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20151112	MGI			PMID:25910808
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19456252
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19456252
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160128	MGI			PMID:24135024
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832488
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0012046	decreased susceptibility to hypertension		IAGP		N	RGD:5509061	20160128	MGI			PMID:24135024
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0015051	abnormal postsynapse morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:18718479
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0015055	decreased synapse density		IAGP		N	RGD:5509061	20260813	MGI			PMID:18718479
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0020510	increased dendritic spine length		IAGP		N	RGD:5509061	20211014	MGI			PMID:18718479
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20190704	MGI			PMID:18718479
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:19456252
11243	Rock2	Rho-associated coiled-coil containing protein kinase 2	gene	MP:0031509	decreased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:24135024
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675006
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906072
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24971615
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675006
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201022	MGI			PMID:32499443
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675006
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675006
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906072
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:24971615
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24971615
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675006
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0004935	epididymis degeneration		IAGP		N	RGD:5509061	20230601	MGI			PMID:37095084
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906072
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:24971615
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0009248	small caput epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8675006
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:24971615
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20201022	MGI			PMID:32499443
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220303	MGI			PMID:10906072
11244	Ros1	Ros1 proto-oncogene, receptor tyrosine kinase	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220303	MGI			PMID:8675006
11247	Rrm1	ribonucleotide reductase M1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:26077802
11247	Rrm1	ribonucleotide reductase M1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
11247	Rrm1	ribonucleotide reductase M1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
11248	Rrm2	ribonucleotide reductase M2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
11248	Rrm2	ribonucleotide reductase M2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11248	Rrm2	ribonucleotide reductase M2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
11249	War	warfarin resistance	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20150514	MGI			PMID:1063212
11249	War	warfarin resistance	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150514	MGI			PMID:1063212
11250	Rxra	retinoid X receptor alpha	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16259011
11250	Rxra	retinoid X receptor alpha	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7638202
11250	Rxra	retinoid X receptor alpha	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20170824	MGI			PMID:10675365
11250	Rxra	retinoid X receptor alpha	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0000288	abnormal pericardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0000299	failure of atrioventricular cushion closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:16259011
11250	Rxra	retinoid X receptor alpha	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0000384	distorted hair follicle pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0000389	disorganized outer root sheath cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16259011
11250	Rxra	retinoid X receptor alpha	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0000597	delayed hepatic development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183441
11250	Rxra	retinoid X receptor alpha	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11250	Rxra	retinoid X receptor alpha	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11250	Rxra	retinoid X receptor alpha	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11250	Rxra	retinoid X receptor alpha	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0001247	dermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0001247	dermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0001247	dermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16259011
11250	Rxra	retinoid X receptor alpha	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16259011
11250	Rxra	retinoid X receptor alpha	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11250	Rxra	retinoid X receptor alpha	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923367
11250	Rxra	retinoid X receptor alpha	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9356169
11250	Rxra	retinoid X receptor alpha	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493527
11250	Rxra	retinoid X receptor alpha	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923367
11250	Rxra	retinoid X receptor alpha	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493527
11250	Rxra	retinoid X receptor alpha	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923367
11250	Rxra	retinoid X receptor alpha	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493527
11250	Rxra	retinoid X receptor alpha	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493527
11250	Rxra	retinoid X receptor alpha	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493527
11250	Rxra	retinoid X receptor alpha	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493527
11250	Rxra	retinoid X receptor alpha	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923367
11250	Rxra	retinoid X receptor alpha	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550726
11250	Rxra	retinoid X receptor alpha	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11250	Rxra	retinoid X receptor alpha	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16259011
11250	Rxra	retinoid X receptor alpha	gene	MP:0002434	abnormal T-helper 2 cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16259011
11250	Rxra	retinoid X receptor alpha	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11250	Rxra	retinoid X receptor alpha	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0003011	delayed dark adaptation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:7638202
11250	Rxra	retinoid X receptor alpha	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183441
11250	Rxra	retinoid X receptor alpha	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0003923	abnormal heart left atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7638202
11250	Rxra	retinoid X receptor alpha	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11250	Rxra	retinoid X receptor alpha	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0004058	abnormal ventricle papillary muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0004062	dilated heart right atrium		IAGP		N	RGD:5509061	20231221	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0004126	thin hypodermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16259011
11250	Rxra	retinoid X receptor alpha	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0004971	dermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9376317
11250	Rxra	retinoid X receptor alpha	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7638202
11250	Rxra	retinoid X receptor alpha	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0006119	mitral valve atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0006122	mitral valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7638202
11250	Rxra	retinoid X receptor alpha	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550726
11250	Rxra	retinoid X receptor alpha	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20200618	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0008117	abnormal Langerhans cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0008244	abnormal peritoneal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0008542	enlarged cervical lymph nodes		IAGP		N	RGD:5509061	20200618	MGI			PMID:16199515
11250	Rxra	retinoid X receptor alpha	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742273
11250	Rxra	retinoid X receptor alpha	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0008860	abnormal hair cycle telogen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0008881	absent Harderian gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183441
11250	Rxra	retinoid X receptor alpha	gene	MP:0009555	abnormal hair follicle melanin granule distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0009612	thick epidermis suprabasal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0009736	abnormal prostate gland branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183441
11250	Rxra	retinoid X receptor alpha	gene	MP:0010064	increased circulating creatine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:7638202
11250	Rxra	retinoid X receptor alpha	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0010455	aortopulmonary window		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0010457	pulmonary artery stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0010584	abnormal conotruncus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0010640	ventricular myocardium compact layer hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0010640	ventricular myocardium compact layer hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0010706	ventral rotation of lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0010707	decreased ventral retina size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0010710	absent sclera		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0010716	optic disk coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0010720	absent sublingual duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493527
11250	Rxra	retinoid X receptor alpha	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550726
11250	Rxra	retinoid X receptor alpha	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20170824	MGI			PMID:10675365
11250	Rxra	retinoid X receptor alpha	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0011369	increased renal glomerulus apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21135166
11250	Rxra	retinoid X receptor alpha	gene	MP:0012501	abnormal pericardial cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0012802	increased rhombomere 5 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0013269	third pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231221	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0021160	decreased heart right ventricle wall thickness		IAGP		N	RGD:5509061	20231221	MGI			PMID:8823298
11250	Rxra	retinoid X receptor alpha	gene	MP:0030335	absent third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:19255444
11250	Rxra	retinoid X receptor alpha	gene	MP:0030570	abnormal piliary canal morphology		IAGP		N	RGD:5509061	20180524	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0030571	dilated piliary canal		IAGP		N	RGD:5509061	20180524	MGI			PMID:11171393
11250	Rxra	retinoid X receptor alpha	gene	MP:0031530	abnormal heart ventricle shape		IAGP		N	RGD:5509061	20240104	MGI			PMID:7638202
11250	Rxra	retinoid X receptor alpha	gene	MP:0031530	abnormal heart ventricle shape		IAGP		N	RGD:5509061	20240104	MGI			PMID:7926783
11250	Rxra	retinoid X receptor alpha	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:7638202
11250	Rxra	retinoid X receptor alpha	gene	MP:0031757	second degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:7638202
11250	Rxra	retinoid X receptor alpha	gene	MP:0031762	third degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:7638202
11251	Rxrb	retinoid X receptor beta	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11251	Rxrb	retinoid X receptor beta	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11251	Rxrb	retinoid X receptor beta	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11251	Rxrb	retinoid X receptor beta	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0001247	dermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883728
11251	Rxrb	retinoid X receptor beta	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883728
11251	Rxrb	retinoid X receptor beta	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883728
11251	Rxrb	retinoid X receptor beta	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11251	Rxrb	retinoid X receptor beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11251	Rxrb	retinoid X receptor beta	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11251	Rxrb	retinoid X receptor beta	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993927
11251	Rxrb	retinoid X receptor beta	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883728
11251	Rxrb	retinoid X receptor beta	gene	MP:0003193	decreased cholesterol efflux		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993927
11251	Rxrb	retinoid X receptor beta	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751185
11251	Rxrb	retinoid X receptor beta	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0004971	dermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20200618	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0008542	enlarged cervical lymph nodes		IAGP		N	RGD:5509061	20200618	MGI			PMID:16199515
11251	Rxrb	retinoid X receptor beta	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0010584	abnormal conotruncus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0010640	ventricular myocardium compact layer hypoplasia		IAGP		N	RGD:5509061	20240118	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0010706	ventral rotation of lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0010716	optic disk coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557197
11251	Rxrb	retinoid X receptor beta	gene	MP:0012802	increased rhombomere 5 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0013269	third pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:19255444
11251	Rxrb	retinoid X receptor beta	gene	MP:0030335	absent third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:19255444
11252	S100b	S100 protein, beta polypeptide, neural	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11872254
11252	S100b	S100 protein, beta polypeptide, neural	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
11252	S100b	S100 protein, beta polypeptide, neural	gene	MP:0003177	allodynia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600520
11252	S100b	S100 protein, beta polypeptide, neural	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20160804	MGI			
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20150108	MGI			
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17194706
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9333241
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701071
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20201231	MGI			
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9333241
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
11254	Sag	S-antigen, retina and pineal gland (arrestin)	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
11258	Atxn1	ataxin 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322884
11258	Atxn1	ataxin 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22053053
11258	Atxn1	ataxin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22053053
11258	Atxn1	ataxin 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
11258	Atxn1	ataxin 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322884
11258	Atxn1	ataxin 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353120
11258	Atxn1	ataxin 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22053053
11258	Atxn1	ataxin 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749985
11258	Atxn1	ataxin 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322884
11258	Atxn1	ataxin 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22053053
11258	Atxn1	ataxin 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23719801
11258	Atxn1	ataxin 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651231
11258	Atxn1	ataxin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651231
11258	Atxn1	ataxin 1	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
11258	Atxn1	ataxin 1	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22053053
11258	Atxn1	ataxin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322884
11258	Atxn1	ataxin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22053053
11258	Atxn1	ataxin 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651231
11258	Atxn1	ataxin 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
11258	Atxn1	ataxin 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322884
11258	Atxn1	ataxin 1	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22053053
11258	Atxn1	ataxin 1	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353120
11258	Atxn1	ataxin 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651231
11258	Atxn1	ataxin 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
11258	Atxn1	ataxin 1	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
11258	Atxn1	ataxin 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322884
11258	Atxn1	ataxin 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
11258	Atxn1	ataxin 1	gene	MP:0010902	abnormal pulmonary alveolar sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
11258	Atxn1	ataxin 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
11258	Atxn1	ataxin 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
11258	Atxn1	ataxin 1	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
11258	Atxn1	ataxin 1	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12086639
11258	Atxn1	ataxin 1	gene	MP:0015020	thin cerebral cortex layer		IAGP		N	RGD:5509061	20260716	MGI			PMID:28288114
11258	Atxn1	ataxin 1	gene	MP:0020594	decreased cerebral cortex cell number		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
11258	Atxn1	ataxin 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:28288114
11259	Scg2	secretogranin II	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20220120	MGI			PMID:33299180
11264658	Traj33	T cell receptor alpha joining 33	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20191003	MGI			PMID:31113973
11266	Scn2b	sodium channel, voltage-gated, type II, beta	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12481039
11266	Scn2b	sodium channel, voltage-gated, type II, beta	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12481039
11266	Scn2b	sodium channel, voltage-gated, type II, beta	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20170323	MGI			
11266	Scn2b	sodium channel, voltage-gated, type II, beta	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20220519	MGI			
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21881211
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0001942	abnormal lung volume		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0004037	increased muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21881211
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21881211
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0009046	muscle twitch		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150219	MGI			PMID:25348630
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18317596
11268	Scn4a	sodium channel, voltage-gated, type IV, alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8589728
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8589728
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8589728
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326675
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:8589728
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857811
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326675
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326675
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326675
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0010109	abnormal renal sodium reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326675
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326675
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8589728
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857811
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0011417	abnormal renal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:20389022
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0011463	decreased urine bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326675
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20170921	MGI			PMID:9326675
11269	Scnn1a	sodium channel, nonvoltage-gated 1 alpha	gene	MP:0014206	decreased intestinal epithelial sodium ion transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:9326675
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:11257137
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:11869685
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11257137
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11257137
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11257137
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11257137
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11869685
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:16860389
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:16860389
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11869685
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11869685
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11869685
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0008761	abnormal immunoglobulin light chain V-J recombination		IAGP		N	RGD:5509061	20160630	MGI			PMID:11869685
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11869685
11269910	Iglc1	immunoglobulin lambda constant 1	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11869685
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990092
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589691
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589691
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589691
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036848
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990093
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990092
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589691
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990092
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0003028	alkalosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589691
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0004119	hypokalemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589691
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589691
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20160421	MGI			
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990092
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0005634	decreased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990092
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589691
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990092
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0010127	hypervolemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589691
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036848
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990092
11272	Scnn1b	sodium channel, nonvoltage-gated 1 beta	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11673458
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11673458
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609524
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553048
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553048
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11673458
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553048
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11673458
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0004774	abnormal bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11673458
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11673458
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553048
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553048
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553048
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11673458
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553048
11273	Scp2	sterol carrier protein 2, liver	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068117
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0000122	premature tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151080
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135576
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257138
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774854
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135576
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093502
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641038
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093502
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9734366
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641038
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001968	abnormal touch/nociception		IAGP		N	RGD:5509061	20220922	MGI			PMID:35775484
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135576
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23603910
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21458307
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728728
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641038
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641140
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002570	alcohol aversion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002620	abnormal monocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17364026
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002620	abnormal monocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463410
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691291
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691291
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691291
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485904
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257138
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21458307
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691291
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003397	increased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135576
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003546	decreased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17301181
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15718500
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257138
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774854
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135576
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431224
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641140
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463410
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135576
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431224
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9884336
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774854
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10395330
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257138
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20220922	MGI			PMID:35775484
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691291
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151080
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431224
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641038
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005098	abnormal optic choroid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9734366
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135576
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:9884336
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691291
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9734366
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093502
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20220922	MGI			PMID:35775484
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093502
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005546	choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005546	choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005549	retina pigment epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641038
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485904
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463410
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0006187	retina deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0006187	retina deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0006238	abnormal choriocapillaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691291
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257138
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23603910
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17301181
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008243	abnormal macrophage derived foam cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257138
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728728
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641038
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257138
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728728
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463410
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641038
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641038
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728728
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257138
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728728
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463410
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463410
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326085
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135576
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641140
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641140
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093502
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691201
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431224
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473219
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691291
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728728
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0009787	increased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641038
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0010016	variable depigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093502
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0010740	abnormal dendritic cell chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23603910
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151080
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728728
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:17135576
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:23637822
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:16691291
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:14566334
11275	Ccl2	C-C motif chemokine ligand 2	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:23637822
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15517609
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729478
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875005
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0002570	alcohol aversion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0003546	decreased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0005614	decreased susceptibility to type III hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15517609
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729478
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729478
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875005
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0020449	decreased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:19729478
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0020938	decreased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:7667639
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0020945	abnormal susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11875005
11276	Ccl3	C-C motif chemokine ligand 3	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11875005
11279	Sdc4	syndecan 4	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
11279	Sdc4	syndecan 4	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160142
11279	Sdc4	syndecan 4	gene	MP:0002546	mydriasis		IEA		N	RGD:5509061	20170105	MGI			
11279	Sdc4	syndecan 4	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:11304570
11279	Sdc4	syndecan 4	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160142
11279	Sdc4	syndecan 4	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681494
11279	Sdc4	syndecan 4	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
11279	Sdc4	syndecan 4	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
11279	Sdc4	syndecan 4	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
11279	Sdc4	syndecan 4	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11304570
11279	Sdc4	syndecan 4	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
11279	Sdc4	syndecan 4	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160142
11279	Sdc4	syndecan 4	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11084653
11279	Sdc4	syndecan 4	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11304570
11279	Sdc4	syndecan 4	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158320
11279	Sdc4	syndecan 4	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
11279	Sdc4	syndecan 4	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
11279	Sdc4	syndecan 4	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
11279	Sdc4	syndecan 4	gene	MP:0009641	kidney degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11304570
11279	Sdc4	syndecan 4	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11304570
11279	Sdc4	syndecan 4	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18158320
11279	Sdc4	syndecan 4	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
11279	Sdc4	syndecan 4	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
11279	Sdc4	syndecan 4	gene	MP:0010238	increased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
11279	Sdc4	syndecan 4	gene	MP:0011333	abnormal kidney inner medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11304570
11279	Sdc4	syndecan 4	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160142
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20833981
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434755
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9634237
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000262	poor arterial differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395391
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434755
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434756
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8757135
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689100
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689100
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689100
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20833981
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0001602	impaired myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689100
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434755
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:12707343
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434755
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434756
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0002982	abnormal primordial germ cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12684531
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035208
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20833981
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20833981
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434755
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434756
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20181227	MGI			
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434755
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434756
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395391
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20833981
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8757135
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8757135
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434756
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434756
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850355
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434755
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434756
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395391
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20181227	MGI			
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:8757135
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20833981
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434756
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8757135
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434755
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8757135
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0011816	decreased pre-pro B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23434756
11280	Cxcl12	C-X-C motif chemokine ligand 12	gene	MP:0014273	abnormal skin vasculature morphology		IAGP		N	RGD:5509061	20230810	MGI			PMID:23395391
11283	Sele	selectin, endothelial cell	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500197
11283	Sele	selectin, endothelial cell	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
11283	Sele	selectin, endothelial cell	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500197
11283	Sele	selectin, endothelial cell	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050049
11283	Sele	selectin, endothelial cell	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500197
11283	Sele	selectin, endothelial cell	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0000324	increased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456770
11283	Sele	selectin, endothelial cell	gene	MP:0000336	decreased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456770
11283	Sele	selectin, endothelial cell	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050049
11283	Sele	selectin, endothelial cell	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
11283	Sele	selectin, endothelial cell	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0001411	spinning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0001492	abnormal pilomotor reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050049
11283	Sele	selectin, endothelial cell	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
11283	Sele	selectin, endothelial cell	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7541306
11283	Sele	selectin, endothelial cell	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11283	Sele	selectin, endothelial cell	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0002346	abnormal lymph node secondary follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0002351	abnormal cervical lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12096034
11283	Sele	selectin, endothelial cell	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
11283	Sele	selectin, endothelial cell	gene	MP:0002534	abnormal type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456770
11283	Sele	selectin, endothelial cell	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050049
11283	Sele	selectin, endothelial cell	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789256
11283	Sele	selectin, endothelial cell	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500197
11283	Sele	selectin, endothelial cell	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
11283	Sele	selectin, endothelial cell	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:9329976
11283	Sele	selectin, endothelial cell	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0008623	increased circulating interleukin-3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500197
11283	Sele	selectin, endothelial cell	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
11283	Sele	selectin, endothelial cell	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500197
11283	Sele	selectin, endothelial cell	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20260219	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20240104	MGI			PMID:11050049
11283	Sele	selectin, endothelial cell	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20240104	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0014351	abnormal spleen B cell follicle shape		IAGP		N	RGD:5509061	20240104	MGI			PMID:11050049
11283	Sele	selectin, endothelial cell	gene	MP:0014899	increased circulating CSF2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:10500197
11283	Sele	selectin, endothelial cell	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:11468173
11283	Sele	selectin, endothelial cell	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:8598043
11283	Sele	selectin, endothelial cell	gene	MP:0020333	enhanced leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:10500197
11284	Selenow	selenoprotein W	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20220120	MGI			PMID:33859201
11284	Selenow	selenoprotein W	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20220120	MGI			PMID:33859201
11284	Selenow	selenoprotein W	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20220120	MGI			PMID:33859201
11284	Selenow	selenoprotein W	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20220120	MGI			PMID:33859201
11284	Selenow	selenoprotein W	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20220120	MGI			PMID:33859201
11284	Selenow	selenoprotein W	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20220120	MGI			PMID:33859201
11284	Selenow	selenoprotein W	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20220120	MGI			PMID:33859201
11284	Selenow	selenoprotein W	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20220120	MGI			PMID:33859201
11284	Selenow	selenoprotein W	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20220120	MGI			PMID:33859201
11285	Mapk10	mitogen-activated protein kinase 10	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174920
11285	Mapk10	mitogen-activated protein kinase 10	gene	MP:0001051	abnormal somatic motor system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528206
11285	Mapk10	mitogen-activated protein kinase 10	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14704277
11285	Mapk10	mitogen-activated protein kinase 10	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14704277
11285	Mapk10	mitogen-activated protein kinase 10	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9349820
11285	Mapk10	mitogen-activated protein kinase 10	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567045
11285	Mapk10	mitogen-activated protein kinase 10	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9349820
11285	Mapk10	mitogen-activated protein kinase 10	gene	MP:0011452	decreased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14704277
11287	Sftpd	surfactant associated protein D	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698462
11287	Sftpd	surfactant associated protein D	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376353
11287	Sftpd	surfactant associated protein D	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376353
11287	Sftpd	surfactant associated protein D	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751757
11287	Sftpd	surfactant associated protein D	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9774472
11287	Sftpd	surfactant associated protein D	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376353
11287	Sftpd	surfactant associated protein D	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16500946
11287	Sftpd	surfactant associated protein D	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751757
11287	Sftpd	surfactant associated protein D	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9774472
11287	Sftpd	surfactant associated protein D	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698462
11287	Sftpd	surfactant associated protein D	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9774472
11287	Sftpd	surfactant associated protein D	gene	MP:0001942	abnormal lung volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9774472
11287	Sftpd	surfactant associated protein D	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376353
11287	Sftpd	surfactant associated protein D	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751757
11287	Sftpd	surfactant associated protein D	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9774472
11287	Sftpd	surfactant associated protein D	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9774472
11287	Sftpd	surfactant associated protein D	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698462
11287	Sftpd	surfactant associated protein D	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376353
11287	Sftpd	surfactant associated protein D	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698462
11287	Sftpd	surfactant associated protein D	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0004781	abnormal surfactant composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698462
11287	Sftpd	surfactant associated protein D	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751757
11287	Sftpd	surfactant associated protein D	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9774472
11287	Sftpd	surfactant associated protein D	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376353
11287	Sftpd	surfactant associated protein D	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751757
11287	Sftpd	surfactant associated protein D	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9774472
11287	Sftpd	surfactant associated protein D	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801980
11287	Sftpd	surfactant associated protein D	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698462
11287	Sftpd	surfactant associated protein D	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698462
11287	Sftpd	surfactant associated protein D	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751757
11287	Sftpd	surfactant associated protein D	gene	MP:0010815	enlarged alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0010815	enlarged alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:9751757
11287	Sftpd	surfactant associated protein D	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376353
11287	Sftpd	surfactant associated protein D	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15310555
11287	Sftpd	surfactant associated protein D	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11698462
11289	Shbg	sex hormone binding globulin	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
11290	Shox2	SHOX homeobox 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141225
11290	Shox2	SHOX homeobox 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372176
11290	Shox2	SHOX homeobox 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141225
11290	Shox2	SHOX homeobox 2	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454626
11290	Shox2	SHOX homeobox 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372176
11290	Shox2	SHOX homeobox 2	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0003228	abnormal sinus venosus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372176
11290	Shox2	SHOX homeobox 2	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24267650
11290	Shox2	SHOX homeobox 2	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0003856	abnormal hindlimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0004349	absent femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0004352	absent humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537395
11290	Shox2	SHOX homeobox 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454626
11290	Shox2	SHOX homeobox 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454626
11290	Shox2	SHOX homeobox 2	gene	MP:0008503	abnormal spinal cord grey matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24267650
11290	Shox2	SHOX homeobox 2	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141225
11290	Shox2	SHOX homeobox 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454626
11290	Shox2	SHOX homeobox 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454626
11290	Shox2	SHOX homeobox 2	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141225
11290	Shox2	SHOX homeobox 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141225
11290	Shox2	SHOX homeobox 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
11290	Shox2	SHOX homeobox 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454626
11290	Shox2	SHOX homeobox 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454626
11290	Shox2	SHOX homeobox 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372176
11290	Shox2	SHOX homeobox 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620086
11290	Shox2	SHOX homeobox 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11290	Shox2	SHOX homeobox 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141225
11290	Shox2	SHOX homeobox 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620086
11290	Shox2	SHOX homeobox 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620086
11290	Shox2	SHOX homeobox 2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
11290	Shox2	SHOX homeobox 2	gene	MP:0021214	anterior cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:16141225
11290	Shox2	SHOX homeobox 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:16141225
11290	Shox2	SHOX homeobox 2	gene	MP:0030330	abnormal temporomandibular joint disk morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:21454626
11290	Shox2	SHOX homeobox 2	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:16141225
11290	Shox2	SHOX homeobox 2	gene	MP:0031542	sinoatrial node hypoplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:23620086
11291488	Trbv13-2	T cell receptor beta, variable 13-2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:17410206
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20210520	MGI			
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210520	MGI			
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20210520	MGI			
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20210520	MGI			
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295	Slc10a1	solute carrier family 10 (sodium/bile acid cotransporter family), member 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210429	MGI			PMID:25641256
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160630	MGI			PMID:20956327
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11123296
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160630	MGI			PMID:20956327
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:11123296
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11123296
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11123296
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20160630	MGI			PMID:8567970
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20956327
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20956327
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20160630	MGI			PMID:11748158
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20160630	MGI			PMID:17056558
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:11123296
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:11123296
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20956327
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20160630	MGI			PMID:20956327
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11123296
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20160630	MGI			PMID:11123296
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20160630	MGI			PMID:10072491
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008781	abnormal B cell apoptosis		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0010337	increased chronic lymphocytic leukemia incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:20956327
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:15199411
11295908	Igha	immunoglobulin heavy constant alpha	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11123296
11296376	Ighd	immunoglobulin heavy constant delta	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:8418208
11296376	Ighd	immunoglobulin heavy constant delta	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:8446604
11296376	Ighd	immunoglobulin heavy constant delta	gene	MP:0002490	abnormal immunoglobulin level		IEA		N	RGD:5509061	20160630	MGI			
11296376	Ighd	immunoglobulin heavy constant delta	gene	MP:0002491	decreased IgD level		IEA		N	RGD:5509061	20180215	MGI			
11296376	Ighd	immunoglobulin heavy constant delta	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20160630	MGI			PMID:8418208
11296376	Ighd	immunoglobulin heavy constant delta	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20160630	MGI			PMID:8446604
11296376	Ighd	immunoglobulin heavy constant delta	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:8446604
11296376	Ighd	immunoglobulin heavy constant delta	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20160630	MGI			PMID:8446604
11296376	Ighd	immunoglobulin heavy constant delta	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20160630	MGI			PMID:8446604
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0000192	abnormal mineral level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807402
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0001771	abnormal circulating magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215439
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0001784	abnormal fluid regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807402
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215439
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003028	alkalosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215439
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003353	decreased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807402
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003353	decreased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003653	decreased skin turgor		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005522	increased circulating atrial natriuretic factor		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005557	increased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005568	increased circulating total protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0005633	increased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0010092	increased circulating magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215439
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0010108	abnormal renal water reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215439
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011295	abnormal tubuloglomerular feedback response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807402
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011296	decreased tubuloglomerular feedback response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215439
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011304	kidney papillary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011304	kidney papillary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011403	pyelonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011404	pyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011424	decreased urine uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011435	increased urine magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011465	abnormal urine urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011470	increased urine creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011471	decreased urine creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0011563	increased urine prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20170921	MGI			PMID:10779555
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0014809	abnormal circulating urea level		IAGP		N	RGD:5509061	20251204	MGI			PMID:20219826
11297	Slc12a1	solute carrier family 12, member 1	gene	MP:0031404	increased tubuloglomerular feedback response		IAGP		N	RGD:5509061	20220630	MGI			PMID:17215439
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:24367518
11299	Slc16a1	solute carrier family 16 (monocarboxylic acid transporters), member 1	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:24367518
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463816
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427250
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427250
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652604
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898223
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463816
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463816
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463816
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:17307644
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898223
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898223
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521591
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275230
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0002204	abnormal synaptic neurotransmitter level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898223
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14980210
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898223
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652604
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521591
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496457
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003444	abnormal neurotransmitter uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003462	abnormal response to novel odor		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003546	decreased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17307644
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003867	increased defecation amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898223
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463816
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427250
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496457
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427250
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005322	abnormal serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427250
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496457
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427250
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463816
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496457
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652604
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427250
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652604
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427250
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17307644
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275230
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275230
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0009854	impaired gastric peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463816
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275230
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427250
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463816
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275230
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652604
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463816
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275230
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0011479	abnormal catecholamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0014961	increased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:9427251
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:19553450
11300	Slc18a2	solute carrier family 18 (vesicular monoamine), member 2	gene	MP:0031717	prolonged corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:10521591
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20201231	MGI			
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9233792
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20201022	MGI			
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0002944	increased lactate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607354
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363892
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0006219	optic nerve degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607354
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607354
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607354
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
11301	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	gene	MP:0030613	dicarboxylic aciduria		IAGP		N	RGD:5509061	20180920	MGI			PMID:9233792
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:22897848
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160630	MGI			PMID:22897848
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002440	abnormal memory B cell morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:16767092
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:9103199
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20200402	MGI			PMID:30287618
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20200402	MGI			PMID:30287618
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20200402	MGI			PMID:30287618
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20210812	MGI			PMID:33193409
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20160630	MGI			PMID:16767092
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20160630	MGI			PMID:22897848
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20160630	MGI			PMID:7892607
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20160630	MGI			PMID:8438159
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008094	absent memory B cells		IAGP		N	RGD:5509061	20160630	MGI			PMID:9103199
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30287618
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20200402	MGI			PMID:30287618
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008100	absent plasma cells		IAGP		N	RGD:5509061	20160630	MGI			PMID:16767092
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:22897848
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30013024
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30287618
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:22431510
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:23027924
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20160630	MGI			PMID:23001146
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:16767092
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:7892607
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:8438159
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9103199
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23680150
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20200402	MGI			PMID:30287618
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20160630	MGI			PMID:21156282
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20210812	MGI			PMID:33193409
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20160630	MGI			PMID:23423996
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30013024
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21339646
11302549	Ighg1	immunoglobulin heavy constant gamma 1 (G1m marker)	gene	MP:0020155	enhanced humoral immune response		IAGP		N	RGD:5509061	20200402	MGI			PMID:30287618
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160630	MGI			PMID:17202317
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:17202317
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20160630	MGI			PMID:17202317
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20160630	MGI			PMID:16751419
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:15922720
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:11884426
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:11733579
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:17899553
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20160630	MGI			PMID:11114377
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20200116	MGI			PMID:16505059
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:22308431
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:15475246
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:1545868
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:15475246
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:1901381
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11148220
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11937563
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20160630	MGI			PMID:18086860
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20160630	MGI			PMID:19727123
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11717190
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:12471099
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:1545868
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:18086860
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9707605
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20160630	MGI			PMID:19727123
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20160630	MGI			PMID:15922720
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20160630	MGI			PMID:10843660
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20160630	MGI			PMID:15922720
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20160630	MGI			PMID:22284419
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20160630	MGI			PMID:16751419
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20160630	MGI			PMID:22284419
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20160630	MGI			PMID:10748243
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20160630	MGI			PMID:22284419
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:16272283
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160630	MGI			PMID:15922720
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160630	MGI			PMID:22284419
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:11937563
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:16272283
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:1545868
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:16204304
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:18086860
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:1901381
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20160630	MGI			PMID:26832406
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160630	MGI			PMID:10640761
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:17899553
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:17899553
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:17899553
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002363	abnormal spleen marginal sinus morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:15004164
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002453	abnormal B lymphocyte antigen presentation		IAGP		N	RGD:5509061	20160630	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20160630	MGI			PMID:15475246
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20160630	MGI			PMID:21987785
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002473	impaired complement classical pathway		IAGP		N	RGD:5509061	20160630	MGI			PMID:21987785
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11937563
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11148220
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002704	tubular nephritis		IAGP		N	RGD:5509061	20160630	MGI			PMID:22284419
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:21987785
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20160630	MGI			PMID:11067910
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20160630	MGI			PMID:22284419
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20160630	MGI			PMID:21683627
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20160630	MGI			PMID:12486099
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20160630	MGI			PMID:20111715
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10748243
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:17202317
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0003901	abnormal PR interval		IAGP		N	RGD:5509061	20160630	MGI			PMID:16751419
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20160630	MGI			PMID:11698422
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20160630	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20160630	MGI			PMID:15448087
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20160630	MGI			PMID:10748243
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20180111	MGI			PMID:24078696
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20160630	MGI			PMID:11698422
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20160630	MGI			PMID:15448087
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20160630	MGI			PMID:8920894
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20160630	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20160630	MGI			PMID:8920894
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20160630	MGI			PMID:11148220
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20160630	MGI			PMID:21378751
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20160630	MGI			PMID:11733579
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11717190
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20111715
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:16204304
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21378751
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:9707605
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20160630	MGI			PMID:16272283
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20160630	MGI			PMID:11748158
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20160630	MGI			PMID:20664169
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:11717190
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:10843660
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20160630	MGI			PMID:15922720
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20160630	MGI			PMID:22308431
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:10843380
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:10843660
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11698422
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20160630	MGI			PMID:10843660
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20160630	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11067910
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11733579
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11733579
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11733579
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008164	abnormal B-1a B cell morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:12471099
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008164	abnormal B-1a B cell morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:9707605
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:9707605
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:12471099
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:12471099
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21378751
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008198	abnormal follicular dendritic cell antigen presentation		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20160630	MGI			PMID:15004164
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:21378751
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11035071
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11717190
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20160630	MGI			PMID:1545868
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20160630	MGI			PMID:15475246
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008213	absent immature B cells		IAGP		N	RGD:5509061	20160630	MGI			PMID:1545868
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:11717190
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20160630	MGI			PMID:11717190
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008240	abnormal spleen marginal zone macrophage morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:15004164
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:15004164
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:17899553
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008401	abnormal CD8-positive, alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:11884426
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:16505059
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:17899553
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20160630	MGI			PMID:15894265
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11148220
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11937563
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9707605
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11148220
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:11148220
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:20133609
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9590224
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20160630	MGI			PMID:9707605
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20160630	MGI			PMID:12471099
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20160630	MGI			PMID:17202317
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20160630	MGI			PMID:17202317
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160630	MGI			PMID:22608497
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:12516557
11303086	Ighm	immunoglobulin heavy constant mu	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:9655395
11303386	Igkj1	immunoglobulin kappa joining 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160630	MGI			PMID:15242641
11303386	Igkj1	immunoglobulin kappa joining 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20160630	MGI			PMID:16703567
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20097878
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0003926	decreased cellular glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0004774	abnormal bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0006353	increased glycosylated hemoglobin level		IEA		N	RGD:5509061	20211021	MGI			
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0009109	decreased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20180614	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23549084
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20097878
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0030589	increased pancreatic alpha cell mass		IAGP		N	RGD:5509061	20180614	MGI			PMID:9354799
11306	Slc2a2	solute carrier family 2 (facilitated glucose transporter), member 2	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:23549084
11307	Slc2a3	solute carrier family 2 (facilitated glucose transporter), member 3	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18780771
11307	Slc2a3	solute carrier family 2 (facilitated glucose transporter), member 3	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18780771
11307	Slc2a3	solute carrier family 2 (facilitated glucose transporter), member 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213475
11307	Slc2a3	solute carrier family 2 (facilitated glucose transporter), member 3	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213475
11307	Slc2a3	solute carrier family 2 (facilitated glucose transporter), member 3	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18780771
11307	Slc2a3	solute carrier family 2 (facilitated glucose transporter), member 3	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:18780771
11307	Slc2a3	solute carrier family 2 (facilitated glucose transporter), member 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213475
11307	Slc2a3	solute carrier family 2 (facilitated glucose transporter), member 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213475
11307	Slc2a3	solute carrier family 2 (facilitated glucose transporter), member 3	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21316350
11308558	Ighe	Immunoglobulin heavy constant epsilon	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20190103	MGI			
11308830	Trgc1	T cell receptor gamma, constant 1	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:15345225
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0002661	abnormal corpus epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673081
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0008003	achlorhydria		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23341620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123620
11311	Slc4a2	solute carrier family 4 (anion exchanger), member 2	gene	MP:0013566	dilated gastric gland		IAGP		N	RGD:5509061	20150312	MGI			PMID:15123620
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124465
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124465
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124465
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124465
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124465
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124465
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0009480	distended cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124465
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124465
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0011435	increased urine magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0011447	abnormal renal glucose reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124465
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0011466	increased urine urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0011923	abnormal bladder urine volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313	Slc5a1	solute carrier family 5 (sodium/glucose cotransporter), member 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23149623
11313297	Trbv14	T cell receptor beta, variable 14	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:15282302
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:28986544
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20160818	MGI			PMID:26075912
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20181115	MGI			PMID:28986544
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20181115	MGI			PMID:28986544
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20181115	MGI			PMID:28986544
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:28986544
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20181115	MGI			PMID:28986544
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0008041	absent NK T cells		IAGP		N	RGD:5509061	20160818	MGI			PMID:26075912
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0008041	absent NK T cells		IAGP		N	RGD:5509061	20181115	MGI			PMID:28986544
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20160818	MGI			PMID:26075912
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0008601	abnormal circulating interleukin-4 level		IAGP		N	RGD:5509061	20160818	MGI			PMID:26075912
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20181115	MGI			PMID:28986544
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0010936	decreased airway resistance		IAGP		N	RGD:5509061	20160818	MGI			PMID:26075912
11313684	Traj18	T cell receptor alpha joining 18	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20181115	MGI			PMID:28986544
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10841514
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208814
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10841514
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208814
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016890
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625138
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873667
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9547354
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9547354
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625138
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16542782
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12598736
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10565817
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625138
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12634480
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15763133
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208814
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16542782
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002635	reduced sensorimotor gating		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208814
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002733	abnormal thermal nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533631
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20260730	MGI			PMID:19179283
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0002798	abnormal active avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625138
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19646988
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003444	abnormal neurotransmitter uptake		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:16542782
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003877	abnormal serotonergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625138
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003958	heart valve hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517274
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21282638
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380550
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10841514
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625138
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0006001	abnormal intestinal transit time		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0006002	abnormal small intestinal transit time		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0006276	abnormal autonomic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599790
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21282638
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208814
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0009713	enhanced conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636213
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21282638
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:10841514
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:16380550
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:9547354
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010758	increased right ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10841514
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0011082	abnormal gastrointestinal motility		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19646988
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0011479	abnormal catecholamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21814181
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0013763	increased T-helper cell number		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20260402	MGI			
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20190718	MGI			PMID:27111230
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20190718	MGI			PMID:22431635
11314	Slc6a4	solute carrier family 6 (neurotransmitter transporter, serotonin), member 4	gene	MP:0020422	decreased freezing behavior		IAGP		N	RGD:5509061	20260730	MGI			PMID:19179283
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22131425
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19750226
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768369
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12617953
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628395
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768369
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754872
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19750538
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152632
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065462
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12617953
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22131425
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12617953
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15710042
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172062
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22131425
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001440	abnormal grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15710042
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9888856
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20201029	MGI			PMID:31365862
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628395
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001746	abnormal pituitary secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172062
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950153
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19750226
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20150723	MGI			PMID:25331903
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:16754872
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20170309	MGI			PMID:26377476
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628395
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201022	MGI			
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15763133
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16865686
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666516
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22267337
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:22034972
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20180405	MGI			PMID:29180115
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20180405	MGI			PMID:29180115
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172062
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20240523	MGI			
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12617953
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20150723	MGI			PMID:25331903
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12617953
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768369
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152632
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223200
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22034972
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20150723	MGI			PMID:25331903
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14980210
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152632
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754872
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19750226
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223200
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768369
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068655
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754872
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003348	hypopituitarism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003444	abnormal neurotransmitter uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754872
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172062
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003462	abnormal response to novel odor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765459
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22131425
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172062
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19750226
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22131425
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004143	muscle hypertonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768369
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768369
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20150723	MGI			PMID:25331903
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:19750226
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950153
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20150723	MGI			PMID:24332984
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20150723	MGI			PMID:25331903
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950153
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005603	neuron hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19750226
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160421	MGI			
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10564358
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227870
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223200
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22131425
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22143804
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152632
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8628395
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520487
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068655
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0005646	abnormal pituitary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22859504
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768369
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008329	decreased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008332	decreased lactotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008365	adenohypophysis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008369	pituitary intermediate lobe hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22131425
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22131425
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172062
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150723	MGI			PMID:25331903
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320258
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754872
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19750226
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20150723	MGI			PMID:25331903
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701073
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009752	enhanced behavioral response to nicotine		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009756	impaired behavioral response to nicotine		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223200
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21057506
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22131425
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20150723	MGI			PMID:25331903
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20180927	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743470
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795541
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841315
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20150723	MGI			PMID:25331903
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20170309	MGI			PMID:26377476
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20180927	MGI			PMID:16754872
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20150611	MGI			PMID:9247269
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150723	MGI			PMID:24332984
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016108
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10564358
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12617953
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21057506
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21057506
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011452	decreased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21057506
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011452	decreased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22143804
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0011975	neuronal cytoplasmic inclusions		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0013218	abnormal substantia nigra pars reticulata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19750226
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0013219	abnormal substantia nigra pars compacta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19750226
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0013219	abnormal substantia nigra pars compacta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914740
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0013219	abnormal substantia nigra pars compacta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152632
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0014365	impaired short-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0014373	increased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:18701073
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0014375	increased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:18701073
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0014381	abnormal miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:22034972
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:27038906
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0030586	impaired behavioral response to amphetamine		IAGP		N	RGD:5509061	20250424	MGI			PMID:32778904
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0030610	absent teeth		IEA		N	RGD:5509061	20201022	MGI			
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:11172062
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12617953
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:16436185
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22034972
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25915474
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:8628395
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:9888856
11315	Slc6a3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20250424	MGI			PMID:32778904
11315710	Trav1	T cell receptor alpha variable 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11316	Slc7a1	solute carrier family 7 (cationic amino acid transporter, y+ system), member 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9106662
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358967
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23904602
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970112
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20241121	MGI			
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970112
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23904602
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23904602
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0008035	behavioral arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20221215	MGI			
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23904602
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0009979	abnormal cerebellum deep nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0009980	abnormal cerebellum dentate nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10199808
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9335342
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0013532	abnormal parotid gland physiology		IAGP		N	RGD:5509061	20160310	MGI			PMID:11358967
11317	Slc9a1	solute carrier family 9 (sodium/hydrogen exchanger), member 1	gene	MP:0014329	abnormal Purkinje cell axon morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:23904602
11317091	Ighg3	Immunoglobulin heavy constant gamma 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0008728	increased memory B cell number		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0008729	decreased memory B cell number		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0008896	increased IgG2c level		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11317092	Ighg2c	immunoglobulin heavy constant gamma 2C	gene	MP:0013654	increased CD103-positive CD11b-low dendritic cell number		IAGP		N	RGD:5509061	20241031	MGI			PMID:35133976
11318	Slc9a2	solute carrier family 9 (sodium/hydrogen exchanger), member 2	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11099134
11318	Slc9a2	solute carrier family 9 (sodium/hydrogen exchanger), member 2	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9502765
11318	Slc9a2	solute carrier family 9 (sodium/hydrogen exchanger), member 2	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11099134
11318	Slc9a2	solute carrier family 9 (sodium/hydrogen exchanger), member 2	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9502765
11318	Slc9a2	solute carrier family 9 (sodium/hydrogen exchanger), member 2	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9502765
11318	Slc9a2	solute carrier family 9 (sodium/hydrogen exchanger), member 2	gene	MP:0008001	hypochlorhydria		IAGP		N	RGD:5509061	20141003	MGI			PMID:9502765
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0000466	esophageal epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0000525	renal tubular acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698654
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0003027	abnormal blood pH regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0006423	dilated rete testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698654
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0009140	dilated efferent ductule of testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11698654
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0009480	distended cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11319	Slc9a3	solute carrier family 9 (sodium/hydrogen exchanger), member 3	gene	MP:0010108	abnormal renal water reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9662405
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160421	MGI			
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15684419
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20160421	MGI			
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0001653	gastric necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15684419
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15684419
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0004138	abnormal mucous neck cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15684419
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15684419
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15684419
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0008001	hypochlorhydria		IAGP		N	RGD:5509061	20141003	MGI			PMID:15684419
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
11320	Slc9a4	solute carrier family 9 (sodium/hydrogen exchanger), member 4	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15684419
11321	Snai2	snail family zinc finger 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
11321	Snai2	snail family zinc finger 2	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20150903	MGI			PMID:18663143
11321	Snai2	snail family zinc finger 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20230601	MGI			
11321	Snai2	snail family zinc finger 2	gene	MP:0000370	head blaze		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
11321	Snai2	snail family zinc finger 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659933
11321	Snai2	snail family zinc finger 2	gene	MP:0001310	abnormal conjunctiva morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659933
11321	Snai2	snail family zinc finger 2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12444107
11321	Snai2	snail family zinc finger 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12444107
11321	Snai2	snail family zinc finger 2	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12398892
11321	Snai2	snail family zinc finger 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12398892
11321	Snai2	snail family zinc finger 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659933
11321	Snai2	snail family zinc finger 2	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659933
11321	Snai2	snail family zinc finger 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
11321	Snai2	snail family zinc finger 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20230601	MGI			
11321	Snai2	snail family zinc finger 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12398892
11321	Snai2	snail family zinc finger 2	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12444107
11321	Snai2	snail family zinc finger 2	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
11321	Snai2	snail family zinc finger 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149208
11321	Snai2	snail family zinc finger 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
11321	Snai2	snail family zinc finger 2	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12398892
11321	Snai2	snail family zinc finger 2	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659933
11321	Snai2	snail family zinc finger 2	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:18663143
11321	Snai2	snail family zinc finger 2	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20150903	MGI			PMID:18663143
11321	Snai2	snail family zinc finger 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0009889	persistence of medial edge epithelium during palatal shelf fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150416	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11321	Snai2	snail family zinc finger 2	gene	MP:0014129	thymus fibrosis		IAGP		N	RGD:5509061	20160324	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0014350	disorganized spleen B cell follicle		IAGP		N	RGD:5509061	20240104	MGI			PMID:23874916
11321	Snai2	snail family zinc finger 2	gene	MP:0030054	decreased forehead pigmentation		IAGP		N	RGD:5509061	20170921	MGI			PMID:12444107
11321	Snai2	snail family zinc finger 2	gene	MP:0030280	short parietal bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:17376812
11321	Snai2	snail family zinc finger 2	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:17376812
11323	Tagln	transgelin	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
11323	Tagln	transgelin	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901360
11323	Tagln	transgelin	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901360
11323	Tagln	transgelin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901360
11323	Tagln	transgelin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311138
11323	Tagln	transgelin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158319
11323	Tagln	transgelin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484601
11323	Tagln	transgelin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20428474
11323	Tagln	transgelin	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
11323	Tagln	transgelin	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080989
11323	Tagln	transgelin	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311138
11323	Tagln	transgelin	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0003622	ischuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
11323	Tagln	transgelin	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
11323	Tagln	transgelin	gene	MP:0004181	abnormal carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
11323	Tagln	transgelin	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20160804	MGI			PMID:25872946
11323	Tagln	transgelin	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
11323	Tagln	transgelin	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0009485	distended ileum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311138
11323	Tagln	transgelin	gene	MP:0010352	gastrointestinal tract polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311138
11323	Tagln	transgelin	gene	MP:0010386	abnormal urinary bladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0010478	intracranial aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
11323	Tagln	transgelin	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
11323	Tagln	transgelin	gene	MP:0011082	abnormal gastrointestinal motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0011503	distended jejunum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11323	Tagln	transgelin	gene	MP:0011513	abnormal vertebral artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693521
11323	Tagln	transgelin	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:18586037
11327892	Trbv19	T cell receptor beta, variable 19	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10464373
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10679476
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001749	suppressed circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9516486
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9516486
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055286
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9724058
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10464373
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055286
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10679476
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10679476
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466888
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004364	thin stria vascularis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055286
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10464373
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466888
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10464373
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466888
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004586	pillar cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466888
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004597	increased susceptibility to noise-induced hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10436316
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004716	abnormal cochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10464373
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10464373
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10679476
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421868
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005252	abnormal Meibomian gland morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10679476
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005356	positive geotaxis		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421868
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10679476
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12485820
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421868
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421868
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20200109	MGI			PMID:18372426
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008512	disorganized retina inner nuclear layer		IAGP		N	RGD:5509061	20200109	MGI			PMID:18372426
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200109	MGI			PMID:18372426
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20200109	MGI			PMID:18372426
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0009421	increased gastrocnemius weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0009423	increased extensor digitorum longus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0009425	increased soleus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0009427	increased tibialis anterior weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9516486
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9516486
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0009935	abnormal Meibomian gland acinus morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493445
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0010226	increased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23729587
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20150212	MGI			PMID:9264557
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:10464373
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10436316
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10464373
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055286
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200109	MGI			PMID:18372426
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200109	MGI			PMID:18372426
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0012320	abnormal body fat mass		IAGP		N	RGD:5509061	20160304	MGI			PMID:25468678
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0013391	abnormal Meibomian gland physiology		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0013392	Meibomian gland inflammation		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:9264557
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0020218	abnormal tear production		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0020220	decreased tear production		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036096
11329	Sod1	superoxide dismutase 1, soluble	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:11493445
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890620
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000798	abnormal frontal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000906	abnormal trigeminal V mesencephalic nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000911	abnormal trigeminal motor nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10762155
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10762155
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21571061
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11527927
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:26427390
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11527927
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10762155
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001602	impaired myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890620
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23862693
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679299
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10762155
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002319	hyperoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002329	abnormal blood gas level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20170914	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20170914	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20170914	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002899	fatigue		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890620
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002899	fatigue		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002899	fatigue		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002899	fatigue		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003027	abnormal blood pH regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003032	hypocapnia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23862693
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003195	calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890620
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226230
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514315
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679299
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890620
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21571061
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20170914	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11527927
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226230
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20170914	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20170914	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005098	abnormal optic choroid morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005113	decreased spinal cord ventral horn cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10762155
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11527927
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20200109	MGI			PMID:26427390
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20170914	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20170914	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927656
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226230
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514315
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0006185	retina hemorrhage		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11527927
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200109	MGI			PMID:26427390
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20160616	MGI			PMID:24985474
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10762155
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0009051	dilated distal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:21571061
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21571061
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11226230
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514315
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927656
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721992
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927656
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011015	decreased body surface temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890620
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497723
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19293248
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8790408
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462746
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12176043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:21571061
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011634	abnormal mitochondrial inner membrane morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011687	decreased epidermal stem cell number		IAGP		N	RGD:5509061	20161103	MGI			PMID:26240345
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20170914	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200109	MGI			PMID:26427390
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200109	MGI			PMID:26427390
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679299
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20170921	MGI			PMID:11677043
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20170921	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23862693
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0013404	decreased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:7493016
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20170914	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:15890620
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:33049519
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:23862693
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014867	increased malondialdehyde level		IAGP		N	RGD:5509061	20260212	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:11226230
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:16959785
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:9927656
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014910	decreased hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:9927656
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0014970	decreased muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0020543	decreased substantia nigra size		IAGP		N	RGD:5509061	20180301	MGI			PMID:10762155
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0030021	increased muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:19776389
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0030612	organic aciduria		IAGP		N	RGD:5509061	20180906	MGI			PMID:9927656
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:21195081
11330	Sod2	superoxide dismutase 2, mitochondrial	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:19293248
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20200402	MGI			PMID:25085920
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:25085920
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787098
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15529385
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15529385
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20200402	MGI			PMID:25085920
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15529385
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200402	MGI			PMID:25085920
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7603981
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0010758	increased right ventricle systolic pressure		IAGP		N	RGD:5509061	20200402	MGI			PMID:25085920
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0014600	increased susceptibility to hyperoxia-induced injury		IAGP		N	RGD:5509061	20250206	MGI			PMID:7603981
11331	Sod3	superoxide dismutase 3, extracellular	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:15529385
11332	Sord	sorbitol dehydrogenase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
11332	Sord	sorbitol dehydrogenase	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18760274
11332	Sord	sorbitol dehydrogenase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:18760274
11332	Sord	sorbitol dehydrogenase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:7708723
11332	Sord	sorbitol dehydrogenase	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7708723
11332	Sord	sorbitol dehydrogenase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
11332	Sord	sorbitol dehydrogenase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
11332	Sord	sorbitol dehydrogenase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9403062
11332	Sord	sorbitol dehydrogenase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20220804	MGI			PMID:35687590
11332	Sord	sorbitol dehydrogenase	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20220804	MGI			PMID:35687590
11332	Sord	sorbitol dehydrogenase	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20241121	MGI			
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505376
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0005134	decreased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0008221	abnormal hippocampal commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0009463	abnormal pituitary infundibular stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505376
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0013337	abnormal adenohypophysis development		IAGP		N	RGD:5509061	20141211	MGI			PMID:23505376
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0013342	bifurcated Rathke's pouch		IAGP		N	RGD:5509061	20141204	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0013351	abnormal Rathke's pouch development		IAGP		N	RGD:5509061	20141218	MGI			PMID:14981518
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0014198	absent pituitary infundibular stalk		IAGP		N	RGD:5509061	20160526	MGI			PMID:23505376
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:14585968
11333	Sox3	SRY (sex determining region Y)-box 3	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:14981518
11334	Sp1	trans-acting transcription factor 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9160753
11334	Sp1	trans-acting transcription factor 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9160753
11334	Sp1	trans-acting transcription factor 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0010128	hypovolemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9160753
11334	Sp1	trans-acting transcription factor 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0011525	abnormal placenta intervillous maternal lacunae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0012099	decreased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0012109	decreased trophoblast glycogen cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:17584888
11334	Sp1	trans-acting transcription factor 1	gene	MP:0030989	decreased spongiotrophoblast cell number		IAGP		N	RGD:5509061	20191219	MGI			PMID:17584888
11335	Sp4	trans-acting transcription factor 4	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16430881
11335	Sp4	trans-acting transcription factor 4	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532028
11335	Sp4	trans-acting transcription factor 4	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532028
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16430881
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660867
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660867
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20634195
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20634195
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532028
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532028
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532028
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532028
11335	Sp4	trans-acting transcription factor 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660867
11335	Sp4	trans-acting transcription factor 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0002635	reduced sensorimotor gating		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532028
11335	Sp4	trans-acting transcription factor 4	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532028
11335	Sp4	trans-acting transcription factor 4	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16430881
11335	Sp4	trans-acting transcription factor 4	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0004085	abnormal heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0004123	abnormal impulse conducting system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16430881
11335	Sp4	trans-acting transcription factor 4	gene	MP:0004124	abnormal Purkinje fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:20634195
11335	Sp4	trans-acting transcription factor 4	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660867
11335	Sp4	trans-acting transcription factor 4	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558077
11335	Sp4	trans-acting transcription factor 4	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0010520	sinoatrial block		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0010637	sinus bradycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007485
11335	Sp4	trans-acting transcription factor 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532028
11335	Sp4	trans-acting transcription factor 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660867
11335	Sp4	trans-acting transcription factor 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16430881
11335	Sp4	trans-acting transcription factor 4	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20634195
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20160804	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20160804	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079140
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20141003	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20141003	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20141003	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748289
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20160804	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079140
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532190
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079140
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079140
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588887
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9524110
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20160804	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10749571
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0006201	vitreous body inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0010096	abnormal incisor color		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20141003	MGI			
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0010251	subcapsular cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:9524110
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0010253	posterior subcapsular cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079140
11336	Sparc	secreted acidic cysteine rich glycoprotein	gene	MP:0010255	cortical cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:9856777
11339	Spn	sialophorin	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20220519	MGI			
11339	Spn	sialophorin	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20200514	MGI			
11339	Spn	sialophorin	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
11339	Spn	sialophorin	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11828253
11339	Spn	sialophorin	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566153
11339	Spn	sialophorin	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
11339	Spn	sialophorin	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20211021	MGI			
11339	Spn	sialophorin	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14662853
11339	Spn	sialophorin	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201231	MGI			
11339	Spn	sialophorin	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7566153
11339	Spn	sialophorin	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9645617
11339	Spn	sialophorin	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
11339	Spn	sialophorin	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20210128	MGI			
11339	Spn	sialophorin	gene	MP:0012443	increased corpus callosum size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
11339	Spn	sialophorin	gene	MP:0012461	increased brain internal capsule size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
11339	Spn	sialophorin	gene	MP:0012465	increased hippocampal fimbria size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
11339	Spn	sialophorin	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12073157
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16939396
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:18050311
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17188882
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18174176
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597759
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714436
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714436
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391016
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845900
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375279
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17188882
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16939396
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20201231	MGI			
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393964
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11278791
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20170314	MGI			PMID:18050311
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15165989
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18174176
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730087
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714436
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714436
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391016
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696588
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466120
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10417195
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391016
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:415980
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:415980
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845900
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597759
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:18050311
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597759
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10417195
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003437
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714436
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411681
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:22991301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15165989
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714436
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18174176
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12073157
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11340	Spp1	secreted phosphoprotein 1	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17211411
11340	Spp1	secreted phosphoprotein 1	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597759
11340	Spp1	secreted phosphoprotein 1	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11340	Spp1	secreted phosphoprotein 1	gene	MP:0003279	aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391016
11340	Spp1	secreted phosphoprotein 1	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181551
11340	Spp1	secreted phosphoprotein 1	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466120
11340	Spp1	secreted phosphoprotein 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17188882
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411681
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849558
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845900
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004822	decreased susceptibility to experimental autoimmune uveoretinitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003437
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004880	lung cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:14977630
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714436
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393964
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9661074
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181551
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:18050311
11340	Spp1	secreted phosphoprotein 1	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181551
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16939396
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714436
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451692
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9525990
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751194
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15165989
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411681
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730087
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597759
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730087
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597759
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6417017
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:17301681
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411681
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10411681
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375279
11340	Spp1	secreted phosphoprotein 1	gene	MP:0006133	calcified artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391016
11340	Spp1	secreted phosphoprotein 1	gene	MP:0006133	calcified artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730087
11340	Spp1	secreted phosphoprotein 1	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714436
11340	Spp1	secreted phosphoprotein 1	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696588
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:14977630
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696588
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17188882
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15165989
11340	Spp1	secreted phosphoprotein 1	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17188882
11340	Spp1	secreted phosphoprotein 1	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16939396
11340	Spp1	secreted phosphoprotein 1	gene	MP:0009645	crystalluria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12506146
11340	Spp1	secreted phosphoprotein 1	gene	MP:0009645	crystalluria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11340	Spp1	secreted phosphoprotein 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845900
11340	Spp1	secreted phosphoprotein 1	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:6417017
11340	Spp1	secreted phosphoprotein 1	gene	MP:0009810	increased urine uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11340	Spp1	secreted phosphoprotein 1	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10417195
11340	Spp1	secreted phosphoprotein 1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20220922	MGI			PMID:16939396
11340	Spp1	secreted phosphoprotein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16939396
11340	Spp1	secreted phosphoprotein 1	gene	MP:0011165	abnormal tooth root development		IAGP		N	RGD:5509061	20160818	MGI			PMID:22991301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0011452	decreased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17188882
11340	Spp1	secreted phosphoprotein 1	gene	MP:0011460	decreased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11340	Spp1	secreted phosphoprotein 1	gene	MP:0011477	abnormal urine nucleoside level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
11340	Spp1	secreted phosphoprotein 1	gene	MP:0014502	decreased circulating protein level		IAGP		N	RGD:5509061	20260219	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0014903	decreased circulating CCL2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:17823662
11340	Spp1	secreted phosphoprotein 1	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20220922	MGI			PMID:16939396
11340	Spp1	secreted phosphoprotein 1	gene	MP:0020416	decreased fibroblast chemotaxis		IAGP		N	RGD:5509061	20170223	MGI			PMID:10825241
11340	Spp1	secreted phosphoprotein 1	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:10657301
11340	Spp1	secreted phosphoprotein 1	gene	MP:0021189	increased bone mineral density of presacral vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:16939396
11340	Spp1	secreted phosphoprotein 1	gene	MP:0021191	increased bone mineral density of lumbar vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:16939396
11340	Spp1	secreted phosphoprotein 1	gene	MP:0031273	decreased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20210617	MGI			PMID:14597759
11340	Spp1	secreted phosphoprotein 1	gene	MP:0031518	calcified aortic valve cusp		IAGP		N	RGD:5509061	20240118	MGI			PMID:12466120
11340121	Trdc	T cell receptor delta, constant region	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20160630	MGI			PMID:22770884
11340121	Trdc	T cell receptor delta, constant region	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160630	MGI			PMID:16878135
11340121	Trdc	T cell receptor delta, constant region	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:16878135
11340121	Trdc	T cell receptor delta, constant region	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:22770884
11340121	Trdc	T cell receptor delta, constant region	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:22770884
11340121	Trdc	T cell receptor delta, constant region	gene	MP:0008348	absent gamma-delta T cells		IAGP		N	RGD:5509061	20160630	MGI			PMID:22770884
11341	Srd5a1	steroid 5 alpha-reductase 1	gene	MP:0000664	small prostate gland anterior lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:11606430
11341	Srd5a1	steroid 5 alpha-reductase 1	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11606430
11341	Srd5a1	steroid 5 alpha-reductase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11606430
11341	Srd5a1	steroid 5 alpha-reductase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8721983
11341	Srd5a1	steroid 5 alpha-reductase 1	gene	MP:0002774	small prostate gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11606430
11341	Srd5a1	steroid 5 alpha-reductase 1	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11606430
11341	Srd5a1	steroid 5 alpha-reductase 1	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:8721983
11350	Star	steroidogenic acute regulatory protein	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0001754	increased circulating corticotropin-releasing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0002774	small prostate gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0002774	small prostate gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0002789	male pseudohermaphroditism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0002789	male pseudohermaphroditism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0004832	enlarged ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:10976923
11350	Star	steroidogenic acute regulatory protein	gene	MP:0005129	increased adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0005147	prostate gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0005148	seminal vesicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0008299	adrenal cortical hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11350	Star	steroidogenic acute regulatory protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326645
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000336	decreased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15947484
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15947484
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340066
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10908145
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17504935
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001881	abnormal mammary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340066
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20180426	MGI			PMID:28930659
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714518
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10908145
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0003838	abnormal milk ejection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340066
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005462	abnormal mast cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714518
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005462	abnormal mast cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15947484
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19833766
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727894
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363300
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363300
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20200402	MGI			PMID:31806625
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340066
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19833766
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0009737	prostate gland cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10908145
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20200402	MGI			PMID:31806625
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010172	abnormal mammary gland epithelium physiology		IAGP		N	RGD:5509061	20160317	MGI			PMID:15340066
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010174	decreased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19833766
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009201
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0011696	absent mast cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714518
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31806625
11351	Stat5a	signal transducer and activator of transcription 5A	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:15340066
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340066
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17504935
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001881	abnormal mammary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340066
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20180426	MGI			PMID:28930659
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714518
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0003838	abnormal milk ejection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340066
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630227
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005462	abnormal mast cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714518
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779039
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19833766
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727894
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22520852
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363300
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363300
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9841920
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340066
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19833766
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599554
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552213
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493008
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010172	abnormal mammary gland epithelium physiology		IAGP		N	RGD:5509061	20160317	MGI			PMID:15340066
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19833766
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010768	mortality/aging		IAGP		N	RGD:5509061	20260430	MGI			PMID:39191751
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20251204	MGI			PMID:40228864
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286195
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0011532	decreased urine major urinary protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0011696	absent mast cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714518
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20150611	MGI			PMID:9207075
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:15340066
11352	Stat5b	signal transducer and activator of transcription 5B	gene	MP:0031434	increased miscarriage rate		IAGP		N	RGD:5509061	20220915	MGI			PMID:9207075
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685171
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685171
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0004909	increased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685171
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685171
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0012172	abnormal amniotic fluid composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685171
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0013598	Leydig cell hypertrophy		IAGP		N	RGD:5509061	20150319	MGI			PMID:11713234
11353	Sult1e1	sulfotransferase family 1E, member 1	gene	MP:0020407	abnormal placental thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:15685171
11354953	Mom21_m	modifier of Min 21 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160729	MGI		Created by mouse qtl pipeline	PMID:17435219
11354953	Mom21_m	modifier of Min 21 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:17435219
11354953	Mom21_m	modifier of Min 21 (mouse)	qtl	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20160804	MGI			PMID:17435219
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15255974
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15255974
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220519	MGI			
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20220519	MGI			
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20220519	MGI			
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657302
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15255974
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657302
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12895513
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657302
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15255974
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657302
11361	Stxbp1	syntaxin binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562480
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122112
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122112
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20211202	MGI			PMID:33529173
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20211202	MGI			PMID:33529173
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562480
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122112
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200227	MGI			PMID:31575858
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20200227	MGI			PMID:31575858
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562480
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20211202	MGI			PMID:33529173
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20200227	MGI			PMID:31575858
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20200227	MGI			PMID:31575858
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0003897	abnormal ST segment duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122112
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20211202	MGI			PMID:33529173
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562480
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122112
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0006135	artery stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122112
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122112
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122112
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11562480
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20211202	MGI			PMID:33529173
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20211202	MGI			PMID:33529173
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0010468	abnormal thoracic aorta morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20211202	MGI			PMID:33529173
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0010575	aortic arch dilation		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20200227	MGI			PMID:31575858
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20200220	MGI			PMID:30089727
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20160602	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:24648545
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0020345	abnormal myocardial fiber currents		IAGP		N	RGD:5509061	20211202	MGI			PMID:33529173
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0031192	coronary artery spasm		IAGP		N	RGD:5509061	20201119	MGI			PMID:12122112
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:11562480
11362	Abcc9	ATP-binding cassette, sub-family C member 9	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:31575858
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761591
11367	Sycp1	synaptonemal complex protein 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937223
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678170
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12004129
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678170
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12004129
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678170
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678170
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12004129
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678170
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678170
11368	Sycp3	synaptonemal complex protein 3	gene	MP:0011954	shortened PQ interval		IEA		N	RGD:5509061	20211021	MGI			
11370	Syn1	synapsin I	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:7777057
11370	Syn1	synapsin I	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902212
11370	Syn1	synapsin I	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:23280234
11370	Syn1	synapsin I	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23280234
11370	Syn1	synapsin I	gene	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568108
11370	Syn1	synapsin I	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23280234
11370	Syn1	synapsin I	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568108
11370	Syn1	synapsin I	gene	MP:0002916	increased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568108
11370	Syn1	synapsin I	gene	MP:0002916	increased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:7777057
11370	Syn1	synapsin I	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902212
11370	Syn1	synapsin I	gene	MP:0002922	decreased post-tetanic potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7777057
11370	Syn1	synapsin I	gene	MP:0002924	delayed CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568107
11370	Syn1	synapsin I	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:10352020
11370	Syn1	synapsin I	gene	MP:0002969	impaired social transmission of food preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:23280234
11370	Syn1	synapsin I	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20151224	MGI			PMID:21621590
11370	Syn1	synapsin I	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10352020
11370	Syn1	synapsin I	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20141003	MGI			PMID:10352020
11370	Syn1	synapsin I	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568108
11370	Syn1	synapsin I	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557745
11370	Syn1	synapsin I	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20151224	MGI			PMID:21621590
11370	Syn1	synapsin I	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557745
11370	Syn1	synapsin I	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9513186
11370	Syn1	synapsin I	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568108
11370	Syn1	synapsin I	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20151224	MGI			PMID:21621590
11370	Syn1	synapsin I	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7568107
11373	Syp	synaptophysin	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10595519
11373	Syp	synaptophysin	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10595519
11373	Syp	synaptophysin	gene	MP:0002064	seizures		IEA		N	RGD:5509061	20150219	MGI			
11373	Syp	synaptophysin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8581936
11373	Syp	synaptophysin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643476
11373	Syp	synaptophysin	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230601	MGI			
11373	Syp	synaptophysin	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10595519
11373	Syp	synaptophysin	gene	MP:0002922	decreased post-tetanic potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10595519
11373	Syp	synaptophysin	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
11373	Syp	synaptophysin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20241121	MGI			
11373	Syp	synaptophysin	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
11379	Tac1	tachykinin 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12427862
11379	Tac1	tachykinin 1	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:11433347
11379	Tac1	tachykinin 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20240314	MGI			
11379	Tac1	tachykinin 1	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482938
11379	Tac1	tachykinin 1	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12427862
11379	Tac1	tachykinin 1	gene	MP:0003280	urinary incontinence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684339
11379	Tac1	tachykinin 1	gene	MP:0010386	abnormal urinary bladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684339
11380	Tacr3	tachykinin receptor 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
11380	Tacr3	tachykinin receptor 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20160421	MGI			PMID:22253416
11380	Tacr3	tachykinin receptor 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558564
11380	Tacr3	tachykinin receptor 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160421	MGI			PMID:22253416
11380	Tacr3	tachykinin receptor 3	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210826	MGI			
11380	Tacr3	tachykinin receptor 3	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558564
11380	Tacr3	tachykinin receptor 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20160421	MGI			PMID:22253416
11380	Tacr3	tachykinin receptor 3	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
11380	Tacr3	tachykinin receptor 3	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20160421	MGI			PMID:22253416
11380	Tacr3	tachykinin receptor 3	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20160421	MGI			PMID:22253416
11380	Tacr3	tachykinin receptor 3	gene	MP:0002798	abnormal active avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558564
11380	Tacr3	tachykinin receptor 3	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558564
11380	Tacr3	tachykinin receptor 3	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20160421	MGI			PMID:22253416
11380	Tacr3	tachykinin receptor 3	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20160421	MGI			PMID:22253416
11380	Tacr3	tachykinin receptor 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
11380	Tacr3	tachykinin receptor 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210520	MGI			
11380	Tacr3	tachykinin receptor 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:1473153
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001606	impaired hematopoiesis		IEA		N	RGD:5509061	20161201	MGI			
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505142
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001836	abnormal antigen presentation via MHC class I		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973281
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001836	abnormal antigen presentation via MHC class I		IAGP		N	RGD:5509061	20141003	MGI			PMID:16299505
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001836	abnormal antigen presentation via MHC class I		IAGP		N	RGD:5509061	20141003	MGI			PMID:17128277
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001837	defective assembly of class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981964
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001838	defective intracellular transport of class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981964
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001838	defective intracellular transport of class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:1473153
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001841	decreased level of surface class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973281
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001841	decreased level of surface class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981964
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001841	decreased level of surface class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:1473153
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9443401
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17562770
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23243279
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973281
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892619
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505142
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0004165	abnormal lateral geniculate nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420446
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420446
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20171214	MGI			PMID:21964024
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973281
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1473153
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12634786
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9443401
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973281
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981964
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17562770
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19721454
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17562770
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118151
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420446
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0009222	increased uterus tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9443401
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420446
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17562770
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20180215	MGI			
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9443401
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9443401
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9443401
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0010839	decreased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20180215	MGI			
11387	Tap1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IEA		N	RGD:5509061	20111116	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001837	defective assembly of class I molecules		IEA		N	RGD:5509061	20111116	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0001841	decreased level of surface class I molecules		IEA		N	RGD:5509061	20111116	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0005078	abnormal cytotoxic T cell physiology		IEA		N	RGD:5509061	20111116	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20180215	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20150205	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19721454
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0010766	abnormal NK cell physiology		IEA		N	RGD:5509061	20111116	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11388	Tap2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210128	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210128	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210128	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20240523	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20210520	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210128	MGI			
11391	Tat	tyrosine aminotransferase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11392	Cntn2	contactin 2	gene	MP:0000576	clubfoot		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
11392	Cntn2	contactin 2	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
11392	Cntn2	contactin 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
11392	Cntn2	contactin 2	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11178983
11392	Cntn2	contactin 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550718
11392	Cntn2	contactin 2	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11178983
11392	Cntn2	contactin 2	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
11392	Cntn2	contactin 2	gene	MP:0004103	abnormal ventral striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
11392	Cntn2	contactin 2	gene	MP:0005423	abnormal somatic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550718
11392	Cntn2	contactin 2	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550718
11392	Cntn2	contactin 2	gene	MP:0008129	absent brain internal capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
11392	Cntn2	contactin 2	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
11392	Cntn2	contactin 2	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
11392	Cntn2	contactin 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:26114544
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20170314	MGI			PMID:26114544
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170314	MGI			PMID:26114544
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:26114544
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20170314	MGI			PMID:26114544
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20170314	MGI			PMID:26114544
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:26114544
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20230907	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231102	MGI			PMID:34129362
11393	Tafazzin	tafazzin, phospholipid-lysophospholipid transacylase	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:34129362
11394	Tbxas1	thromboxane A synthase 1, platelet	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15010374
11394	Tbxas1	thromboxane A synthase 1, platelet	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:15010374
11394	Tbxas1	thromboxane A synthase 1, platelet	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15010374
11395	Eloa	elongin A	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
11395	Eloa	elongin A	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0000597	delayed hepatic development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
11395	Eloa	elongin A	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
11395	Eloa	elongin A	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
11395	Eloa	elongin A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
11395	Eloa	elongin A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20210826	MGI			
11395	Eloa	elongin A	gene	MP:0001889	delayed brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
11395	Eloa	elongin A	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
11395	Eloa	elongin A	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11395	Eloa	elongin A	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17170753
11395	Eloa	elongin A	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17170753
11397	Hnf1a	HNF1 homeobox A	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529398
11397	Hnf1a	HNF1 homeobox A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529398
11397	Hnf1a	HNF1 homeobox A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:9593777
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529398
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529398
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529398
11397	Hnf1a	HNF1 homeobox A	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529398
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529398
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0002985	abnormal urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20181220	MGI			PMID:9593777
11397	Hnf1a	HNF1 homeobox A	gene	MP:0003311	aminoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0003325	decreased liver function		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20181220	MGI			PMID:9593777
11397	Hnf1a	HNF1 homeobox A	gene	MP:0008822	decreased blood uric acid level		IAGP		N	RGD:5509061	20240912	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0009109	decreased pancreas weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:9593777
11397	Hnf1a	HNF1 homeobox A	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20181220	MGI			PMID:9593777
11397	Hnf1a	HNF1 homeobox A	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20181220	MGI			PMID:9593777
11397	Hnf1a	HNF1 homeobox A	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0009810	increased urine uric acid level		IAGP		N	RGD:5509061	20161208	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9566924
11397	Hnf1a	HNF1 homeobox A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161208	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0011447	abnormal renal glucose reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0011765	oroticaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0020401	argininuria		IAGP		N	RGD:5509061	20161208	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0030662	decreased circulating arginine level		IAGP		N	RGD:5509061	20240912	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0030670	increased circulating phenylalanine level		IAGP		N	RGD:5509061	20240912	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0030681	increased circulating hydroxyproline level		IAGP		N	RGD:5509061	20240912	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0030682	hydroxyprolinuria		IAGP		N	RGD:5509061	20240912	MGI			PMID:8598044
11397	Hnf1a	HNF1 homeobox A	gene	MP:0030719	decreased circulating lysine level		IAGP		N	RGD:5509061	20240912	MGI			PMID:8598044
11398	Hnf1b	HNF1 homeobox B	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362348
11398	Hnf1b	HNF1 homeobox B	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518495
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518495
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518495
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518495
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362348
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002138	abnormal hepatobiliary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002139	abnormal hepatobiliary system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518495
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518495
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362348
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0003252	abnormal bile duct physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0003325	decreased liver function		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0003334	pancreas fibrosis		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0003338	pancreas lipomatosis		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0003341	chronic pancreas inflammation		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518495
11398	Hnf1b	HNF1 homeobox B	gene	MP:0004755	abnormal loop of Henle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362348
11398	Hnf1b	HNF1 homeobox B	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362348
11398	Hnf1b	HNF1 homeobox B	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0005415	intrahepatic cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009143	abnormal pancreatic duct morphology		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009149	decreased pancreatic acinar cell number		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009154	pancreatic acinar hypoplasia		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009492	abnormal gallbladder epithelium morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009493	abnormal cystic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009497	abnormal intrahepatic bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009498	abnormal extrahepatic bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0009500	abnormal interlobular bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934849
11398	Hnf1b	HNF1 homeobox B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362348
11398	Hnf1b	HNF1 homeobox B	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518495
11398	Hnf1b	HNF1 homeobox B	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518495
11398	Hnf1b	HNF1 homeobox B	gene	MP:0011198	absent proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0011207	absent ectoplacental cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362348
11398	Hnf1b	HNF1 homeobox B	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362348
11398	Hnf1b	HNF1 homeobox B	gene	MP:0012158	absent visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0012162	absent parietal endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518496
11398	Hnf1b	HNF1 homeobox B	gene	MP:0013221	pancreatic acinar-to-ductal metaplasia		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11398	Hnf1b	HNF1 homeobox B	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20210701	MGI			PMID:33527355
11399	Tcp1	t-complex protein 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20260402	MGI			
11399	Tcp1	t-complex protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
11402	Tcrb	T cell receptor beta chain	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
11402	Tcrb	T cell receptor beta chain	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
11402	Tcrb	T cell receptor beta chain	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017966
11402	Tcrb	T cell receptor beta chain	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:1359428
11402	Tcrb	T cell receptor beta chain	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18997009
11402	Tcrb	T cell receptor beta chain	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103410
11402	Tcrb	T cell receptor beta chain	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103410
11402	Tcrb	T cell receptor beta chain	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964276
11402	Tcrb	T cell receptor beta chain	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18997009
11402	Tcrb	T cell receptor beta chain	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937563
11402	Tcrb	T cell receptor beta chain	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16272283
11402	Tcrb	T cell receptor beta chain	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15770700
11402	Tcrb	T cell receptor beta chain	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1359428
11402	Tcrb	T cell receptor beta chain	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
11402	Tcrb	T cell receptor beta chain	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10850719
11402	Tcrb	T cell receptor beta chain	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1359428
11402	Tcrb	T cell receptor beta chain	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
11402	Tcrb	T cell receptor beta chain	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18997009
11402	Tcrb	T cell receptor beta chain	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
11402	Tcrb	T cell receptor beta chain	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16272283
11402	Tcrb	T cell receptor beta chain	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937563
11402	Tcrb	T cell receptor beta chain	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16272283
11402	Tcrb	T cell receptor beta chain	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075933
11402	Tcrb	T cell receptor beta chain	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17410206
11402	Tcrb	T cell receptor beta chain	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
11402	Tcrb	T cell receptor beta chain	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847251
11402	Tcrb	T cell receptor beta chain	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
11402	Tcrb	T cell receptor beta chain	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19380806
11402	Tcrb	T cell receptor beta chain	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937563
11402	Tcrb	T cell receptor beta chain	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103410
11402	Tcrb	T cell receptor beta chain	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15770700
11402	Tcrb	T cell receptor beta chain	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8104709
11402	Tcrb	T cell receptor beta chain	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18997009
11402	Tcrb	T cell receptor beta chain	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:1359428
11402	Tcrb	T cell receptor beta chain	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017966
11402	Tcrb	T cell receptor beta chain	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075933
11402	Tcrb	T cell receptor beta chain	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103410
11402	Tcrb	T cell receptor beta chain	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
11402	Tcrb	T cell receptor beta chain	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15770700
11402	Tcrb	T cell receptor beta chain	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15770700
11402	Tcrb	T cell receptor beta chain	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075933
11402	Tcrb	T cell receptor beta chain	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10850719
11402	Tcrb	T cell receptor beta chain	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16272283
11402	Tcrb	T cell receptor beta chain	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
11402	Tcrb	T cell receptor beta chain	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1359428
11402	Tcrb	T cell receptor beta chain	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
11402	Tcrb	T cell receptor beta chain	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964276
11402	Tcrb	T cell receptor beta chain	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19380806
11402	Tcrb	T cell receptor beta chain	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1359428
11402	Tcrb	T cell receptor beta chain	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
11402	Tcrb	T cell receptor beta chain	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
11402	Tcrb	T cell receptor beta chain	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1359428
11402	Tcrb	T cell receptor beta chain	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19380806
11402	Tcrb	T cell receptor beta chain	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19380806
11402	Tcrb	T cell receptor beta chain	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017966
11402	Tcrb	T cell receptor beta chain	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0008188	abnormal transitional stage B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0008348	absent gamma-delta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
11402	Tcrb	T cell receptor beta chain	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937563
11402	Tcrb	T cell receptor beta chain	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12530977
11402	Tcrb	T cell receptor beta chain	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250443
11402	Tcrb	T cell receptor beta chain	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19070901
11402	Tcrb	T cell receptor beta chain	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19380806
11402	Tcrb	T cell receptor beta chain	gene	MP:0009925	increased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0010229	increased transitional stage T3 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
11402	Tcrb	T cell receptor beta chain	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
11402	Tcrb	T cell receptor beta chain	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:22585710
11403	Tcrg	T cell receptor gamma chain	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242214
11403	Tcrg	T cell receptor gamma chain	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034115
11403	Tcrg	T cell receptor gamma chain	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034115
11403	Tcrg	T cell receptor gamma chain	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034115
11403	Tcrg	T cell receptor gamma chain	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034115
11403	Tcrg	T cell receptor gamma chain	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9497293
11403	Tcrg	T cell receptor gamma chain	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034115
11403	Tcrg	T cell receptor gamma chain	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242214
11403	Tcrg	T cell receptor gamma chain	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242214
11403	Tcrg	T cell receptor gamma chain	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034115
11403	Tcrg	T cell receptor gamma chain	gene	MP:0005074	impaired granulocyte bactericidal activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034115
11403	Tcrg	T cell receptor gamma chain	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16034115
11403	Tcrg	T cell receptor gamma chain	gene	MP:0008348	absent gamma-delta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242214
11403	Tcrg	T cell receptor gamma chain	gene	MP:0008356	abnormal gamma-delta T cell differentiation		IAGP		N	RGD:5509061	20221201	MGI			PMID:11911829
11403	Tcrg	T cell receptor gamma chain	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242214
11403	Tcrg	T cell receptor gamma chain	gene	MP:0008757	abnormal T cell receptor gamma chain V-J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378791
11403	Tcrg	T cell receptor gamma chain	gene	MP:0008757	abnormal T cell receptor gamma chain V-J recombination		IAGP		N	RGD:5509061	20221201	MGI			PMID:11911829
11404	Tead2	TEA domain family member 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
11404	Tead2	TEA domain family member 2	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
11404	Tead2	TEA domain family member 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17868131
11404	Tead2	TEA domain family member 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
11404	Tead2	TEA domain family member 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
11404	Tead2	TEA domain family member 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17868131
11404	Tead2	TEA domain family member 2	gene	MP:0013217	abnormal posterior definitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
11404	Tead2	TEA domain family member 2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:18332127
11405	Tmbim6	transmembrane BAX inhibitor motif containing 6	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304216
11405	Tmbim6	transmembrane BAX inhibitor motif containing 6	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304216
11406	Trf	transferrin	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20210520	MGI			
11406	Trf	transferrin	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
11406	Trf	transferrin	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210520	MGI			
11406	Trf	transferrin	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20210520	MGI			
11406	Trf	transferrin	gene	MP:0001565	abnormal circulating phosphate level		IEA		N	RGD:5509061	20210520	MGI			
11406	Trf	transferrin	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
11406	Trf	transferrin	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20240523	MGI			
11406	Trf	transferrin	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20201022	MGI			
11406	Trf	transferrin	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20200514	MGI			
11406	Trf	transferrin	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
11406	Trf	transferrin	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0005638	hemochromatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0008387	hypochromic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
11406	Trf	transferrin	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:3681112
11406	Trf	transferrin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11406	Trf	transferrin	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20241121	MGI			
11407	Tff3	trefoil factor 3, intestinal	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8824194
11407	Tff3	trefoil factor 3, intestinal	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:8824194
11407	Tff3	trefoil factor 3, intestinal	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8824194
11408	Tg	thyroglobulin	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:3803305
11408	Tg	thyroglobulin	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
11408	Tg	thyroglobulin	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:1508304
11408	Tg	thyroglobulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1508304
11408	Tg	thyroglobulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:3803305
11408	Tg	thyroglobulin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151119	MGI			PMID:22724066
11408	Tg	thyroglobulin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
11408	Tg	thyroglobulin	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20260402	MGI			
11408	Tg	thyroglobulin	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20260402	MGI			
11408	Tg	thyroglobulin	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
11408	Tg	thyroglobulin	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
11408	Tg	thyroglobulin	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20190502	MGI			
11408	Tg	thyroglobulin	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3803305
11408	Tg	thyroglobulin	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20151119	MGI			PMID:22724066
11408	Tg	thyroglobulin	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
11408	Tg	thyroglobulin	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1508304
11408	Tg	thyroglobulin	gene	MP:0002427	disproportionate dwarf		IEA		N	RGD:5509061	20111116	MGI			
11408	Tg	thyroglobulin	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20181025	MGI			
11408	Tg	thyroglobulin	gene	MP:0002497	increased IgE level		IEA		N	RGD:5509061	20190411	MGI			
11408	Tg	thyroglobulin	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20230601	MGI			
11408	Tg	thyroglobulin	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181025	MGI			
11408	Tg	thyroglobulin	gene	MP:0002865	increased growth rate		IEA		N	RGD:5509061	20111116	MGI			
11408	Tg	thyroglobulin	gene	MP:0003109	short femur		IEA		N	RGD:5509061	20181025	MGI			
11408	Tg	thyroglobulin	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20181025	MGI			
11408	Tg	thyroglobulin	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20181025	MGI			
11408	Tg	thyroglobulin	gene	MP:0004696	abnormal thyroid follicle morphology		IEA		N	RGD:5509061	20111116	MGI			
11408	Tg	thyroglobulin	gene	MP:0004697	abnormal thyroid follicular cell morphology		IEA		N	RGD:5509061	20111116	MGI			
11408	Tg	thyroglobulin	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20181025	MGI			
11408	Tg	thyroglobulin	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3803305
11408	Tg	thyroglobulin	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
11408	Tg	thyroglobulin	gene	MP:0005355	enlarged thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:3803305
11408	Tg	thyroglobulin	gene	MP:0005425	increased macrophage cell number		IEA		N	RGD:5509061	20190411	MGI			
11408	Tg	thyroglobulin	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3803305
11408	Tg	thyroglobulin	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3803305
11408	Tg	thyroglobulin	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
11408	Tg	thyroglobulin	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
11408	Tg	thyroglobulin	gene	MP:0008167	increased B-1a cell number		IEA		N	RGD:5509061	20190411	MGI			
11408	Tg	thyroglobulin	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20190411	MGI			
11408	Tg	thyroglobulin	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20181025	MGI			
11408	Tg	thyroglobulin	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
11408	Tg	thyroglobulin	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20231207	MGI			
11408	Tg	thyroglobulin	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
11408	Tg	thyroglobulin	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
11408	Tg	thyroglobulin	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20190411	MGI			
11408	Tg	thyroglobulin	gene	MP:0014143	decreased body fat mass		IEA		N	RGD:5509061	20181025	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20111208	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477444
11411	Tgfa	transforming growth factor alpha	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0000396	increased curvature of hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477444
11411	Tgfa	transforming growth factor alpha	gene	MP:0000402	abnormal zigzag hair morphology		IEA		N	RGD:5509061	20111116	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456865
11411	Tgfa	transforming growth factor alpha	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477444
11411	Tgfa	transforming growth factor alpha	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
11411	Tgfa	transforming growth factor alpha	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
11411	Tgfa	transforming growth factor alpha	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477444
11411	Tgfa	transforming growth factor alpha	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0001278	kinked vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0001279	wavy vibrissae		IEA		N	RGD:5509061	20111116	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:13358719
11411	Tgfa	transforming growth factor alpha	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:13358719
11411	Tgfa	transforming growth factor alpha	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456865
11411	Tgfa	transforming growth factor alpha	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477444
11411	Tgfa	transforming growth factor alpha	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477444
11411	Tgfa	transforming growth factor alpha	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:13358719
11411	Tgfa	transforming growth factor alpha	gene	MP:0001316	cornea scarring		IAGP		N	RGD:5509061	20141003	MGI			PMID:13358719
11411	Tgfa	transforming growth factor alpha	gene	MP:0001316	cornea scarring		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20111116	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
11411	Tgfa	transforming growth factor alpha	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:13358719
11411	Tgfa	transforming growth factor alpha	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0002074	abnormal hair texture		IEA		N	RGD:5509061	20111116	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20111116	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0002580	duodenal lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
11411	Tgfa	transforming growth factor alpha	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
11411	Tgfa	transforming growth factor alpha	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0003095	abnormal cornea stroma development		IAGP		N	RGD:5509061	20141003	MGI			PMID:13358719
11411	Tgfa	transforming growth factor alpha	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
11411	Tgfa	transforming growth factor alpha	gene	MP:0003671	abnormal eyelid aperture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0003704	abnormal hair follicle development		IEA		N	RGD:5509061	20111116	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0004285	absent Descemet membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15366372
11411	Tgfa	transforming growth factor alpha	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438495
11411	Tgfa	transforming growth factor alpha	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0006194	keratoconjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:13358719
11411	Tgfa	transforming growth factor alpha	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20141225	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:13358719
11411	Tgfa	transforming growth factor alpha	gene	MP:0009272	decreased guard hair length		IEA		N	RGD:5509061	20111116	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20141225	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0009742	increased cornea stroma thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:13358719
11411	Tgfa	transforming growth factor alpha	gene	MP:0010099	abnormal thoracic cage shape		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0010709	absent eye anterior chamber		IAGP		N	RGD:5509061	20141225	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0013389	Meibomian gland hypoplasia		IAGP		N	RGD:5509061	20141225	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0013396	eyelid hyperplasia		IAGP		N	RGD:5509061	20141225	MGI			PMID:8477445
11411	Tgfa	transforming growth factor alpha	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20150402	MGI			PMID:10331984
11411	Tgfa	transforming growth factor alpha	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20260402	MGI			
11411	Tgfa	transforming growth factor alpha	gene	MP:0030175	orbicularis oculi muscle hypoplasia		IAGP		N	RGD:5509061	20171005	MGI			PMID:8477445
11414	Th	tyrosine hydroxylase	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040852
11414	Th	tyrosine hydroxylase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040852
11414	Th	tyrosine hydroxylase	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040852
11414	Th	tyrosine hydroxylase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12704806
11414	Th	tyrosine hydroxylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701681
11414	Th	tyrosine hydroxylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20180913	MGI			PMID:22764207
11414	Th	tyrosine hydroxylase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20251204	MGI			PMID:28949038
11414	Th	tyrosine hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20251030	MGI			PMID:26220941
11414	Th	tyrosine hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20251204	MGI			PMID:28949038
11414	Th	tyrosine hydroxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20251030	MGI			PMID:26220941
11414	Th	tyrosine hydroxylase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040852
11414	Th	tyrosine hydroxylase	gene	MP:0001428	adipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704516
11414	Th	tyrosine hydroxylase	gene	MP:0001462	abnormal avoidance learning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19864633
11414	Th	tyrosine hydroxylase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040852
11414	Th	tyrosine hydroxylase	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040852
11414	Th	tyrosine hydroxylase	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040852
11414	Th	tyrosine hydroxylase	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20180913	MGI			PMID:22764207
11414	Th	tyrosine hydroxylase	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704516
11414	Th	tyrosine hydroxylase	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704516
11414	Th	tyrosine hydroxylase	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701681
11414	Th	tyrosine hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764243
11414	Th	tyrosine hydroxylase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452869
11414	Th	tyrosine hydroxylase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876957
11414	Th	tyrosine hydroxylase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19116659
11414	Th	tyrosine hydroxylase	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701681
11414	Th	tyrosine hydroxylase	gene	MP:0002316	anoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0002798	abnormal active avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704516
11414	Th	tyrosine hydroxylase	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704516
11414	Th	tyrosine hydroxylase	gene	MP:0002822	catalepsy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701681
11414	Th	tyrosine hydroxylase	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20251204	MGI			PMID:28949038
11414	Th	tyrosine hydroxylase	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0003897	abnormal ST segment duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0003908	decreased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0003962	abnormal adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0003962	abnormal adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704516
11414	Th	tyrosine hydroxylase	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701681
11414	Th	tyrosine hydroxylase	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12704806
11414	Th	tyrosine hydroxylase	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20251204	MGI			PMID:28949038
11414	Th	tyrosine hydroxylase	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764243
11414	Th	tyrosine hydroxylase	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20251030	MGI			PMID:26220941
11414	Th	tyrosine hydroxylase	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20251204	MGI			PMID:28949038
11414	Th	tyrosine hydroxylase	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764243
11414	Th	tyrosine hydroxylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20251030	MGI			PMID:26220941
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12704806
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701681
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19864633
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22027820
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764243
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8548806
11414	Th	tyrosine hydroxylase	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701681
11414	Th	tyrosine hydroxylase	gene	MP:0008504	abnormal adrenal chromaffin cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0009078	adrenal gland hyperplasia		IAGP		N	RGD:5509061	20180913	MGI			PMID:22764207
11414	Th	tyrosine hydroxylase	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20251030	MGI			PMID:26220941
11414	Th	tyrosine hydroxylase	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
11414	Th	tyrosine hydroxylase	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0010017	visceral vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0010021	heart vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:12704806
11414	Th	tyrosine hydroxylase	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20251030	MGI			PMID:26220941
11414	Th	tyrosine hydroxylase	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040852
11414	Th	tyrosine hydroxylase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701681
11414	Th	tyrosine hydroxylase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876957
11414	Th	tyrosine hydroxylase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33208756
11414	Th	tyrosine hydroxylase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11414	Th	tyrosine hydroxylase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7592982
11414	Th	tyrosine hydroxylase	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518589
11414	Th	tyrosine hydroxylase	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723393
11414	Th	tyrosine hydroxylase	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20180920	MGI			PMID:12704806
11414	Th	tyrosine hydroxylase	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20251030	MGI			PMID:26220941
11414	Th	tyrosine hydroxylase	gene	MP:0020843	abnormal type I cell of carotid body physiology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38706960
11414	Th	tyrosine hydroxylase	gene	MP:0020875	decreased nervous system dopamine level		IAGP		N	RGD:5509061	20251030	MGI			PMID:26220941
11414	Th	tyrosine hydroxylase	gene	MP:0031252	abnormal physiological response to hypoxia		IAGP		N	RGD:5509061	20210729	MGI			PMID:31848220
11414	Th	tyrosine hydroxylase	gene	MP:0031613	fetal cardiomyocyte disarray		IAGP		N	RGD:5509061	20240509	MGI			PMID:7715703
11414	Th	tyrosine hydroxylase	gene	MP:0031614	fetal cardiomyocyte vacuoles		IAGP		N	RGD:5509061	20240509	MGI			PMID:7715703
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000478	delayed intestine development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416151
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416151
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16131613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:29205102
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16131613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12356724
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304375
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210747
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16131613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20170105	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001454	abnormal cued conditioning behavior		IEA		N	RGD:5509061	20260402	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:16131613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001469	abnormal contextual conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20181227	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001629	abnormal heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12356724
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726557
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304375
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210747
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002710	increased glucagon secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20190725	MGI			PMID:29205102
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002876	abnormal thyroid gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20190725	MGI			PMID:29205102
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:9430637
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16131613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739404
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20190725	MGI			PMID:29205102
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416151
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003498	thyroid gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003499	thyroid gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003502	increased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9430637
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20181227	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20210520	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003965	abnormal pituitary hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210747
11415	Thra	thyroid hormone receptor alpha	gene	MP:0003971	abnormal thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16803873
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004433	abnormal cochlear inner hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004437	decreased cochlear outer hair cell electromotility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004591	enlarged tectorial membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004664	delayed inner ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726557
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004706	short vertebral body		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210747
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304375
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005119	decreased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601836
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210747
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210747
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005135	increased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210747
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005135	increased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210747
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210747
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159823
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9430637
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601836
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005468	abnormal thyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726557
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005474	increased triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005474	increased triiodothyronine level		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005474	increased triiodothyronine level		IAGP		N	RGD:5509061	20190725	MGI			PMID:29205102
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005477	increased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005477	increased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005477	increased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601836
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005477	increased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005477	increased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159823
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726557
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11726557
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005480	increased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11734632
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005480	increased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005480	increased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005480	increased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601836
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005480	increased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739404
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005480	increased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:9430637
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210826	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416151
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159823
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0006394	abnormal vertebral epiphyseal plate morphology		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0006399	abnormal long bone epiphyseal ossification zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0006399	abnormal long bone epiphyseal ossification zone morphology		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0008142	decreased small intestinal villus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416151
11415	Thra	thyroid hormone receptor alpha	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416151
11415	Thra	thyroid hormone receptor alpha	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20190725	MGI			PMID:29205102
11415	Thra	thyroid hormone receptor alpha	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20190725	MGI			PMID:29205102
11415	Thra	thyroid hormone receptor alpha	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327419
11415	Thra	thyroid hormone receptor alpha	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065405
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010122	abnormal bone mineral content		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159823
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20260806	MGI			PMID:29229863
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010964	increased compact bone volume		IAGP		N	RGD:5509061	20150827	MGI			PMID:24914936
11415	Thra	thyroid hormone receptor alpha	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12356724
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17622582
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190725	MGI			PMID:29205102
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12356724
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21914860
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20181227	MGI			
11415	Thra	thyroid hormone receptor alpha	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20150319	MGI			PMID:11731613
11415	Thra	thyroid hormone receptor alpha	gene	MP:0013958	decreased small intestine length		IAGP		N	RGD:5509061	20160414	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20160414	MGI			PMID:11416151
11415	Thra	thyroid hormone receptor alpha	gene	MP:0014091	abnormal tectorial membrane striated-sheet matrix morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:11739587
11415	Thra	thyroid hormone receptor alpha	gene	MP:0014296	delayed skeletal maturation		IAGP		N	RGD:5509061	20230824	MGI			PMID:9927422
11415	Thra	thyroid hormone receptor alpha	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:12869545
11415	Thra	thyroid hormone receptor alpha	gene	MP:0030020	decreased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:15304375
11415	Thra	thyroid hormone receptor alpha	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:16051666
11415	Thra	thyroid hormone receptor alpha	gene	MP:0030388	large fontanelles		IAGP		N	RGD:5509061	20171207	MGI			PMID:16051666
11417	Thrsp	thyroid hormone responsive	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890771
11417	Thrsp	thyroid hormone responsive	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890771
11417	Thrsp	thyroid hormone responsive	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890771
11417	Thrsp	thyroid hormone responsive	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890771
11418	Thy1	thymus cell antigen 1, theta	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:8587606
11418	Thy1	thymus cell antigen 1, theta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:12031407
11418	Thy1	thymus cell antigen 1, theta	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:16049324
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23524300
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23144462
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23524300
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15262835
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23144462
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560951
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778336
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560951
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19128402
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15262835
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19806081
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560951
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15262835
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560952
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322543
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322543
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560952
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560951
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19806081
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560951
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23144462
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560951
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778336
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23524300
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560951
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560951
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15262835
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15262835
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23524300
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778336
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408187
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0003822	decreased left ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15262835
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0003824	decreased left ventricle developed pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15262835
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322543
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15262835
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778336
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12147610
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560951
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12147610
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20150319	MGI			PMID:24736588
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322543
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20150319	MGI			PMID:24736588
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23524300
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15262835
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0006026	dilated terminal bronchiole tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499643
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499643
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19128402
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0006083	abnormal blood vessel elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23524300
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0006237	abnormal choroid vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408187
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11560952
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322543
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20150319	MGI			PMID:24736588
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0008987	abnormal liver lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322543
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322543
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037568
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210617	MGI			PMID:23144462
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23144462
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0009870	abnormal abdominal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23144462
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20160421	MGI			
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0010139	aortitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23144462
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0010659	abdominal aorta aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:23144462
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0011031	abnormal branching involved in terminal bronchiole morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499643
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0014474	decreased pulmonary alveolus wall thickness		IAGP		N	RGD:5509061	20240704	MGI			PMID:19128402
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20180125	MGI			PMID:24736588
11419	Timp3	tissue inhibitor of metalloproteinase 3	gene	MP:0031274	increased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20210617	MGI			PMID:23144462
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21345181
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10401665
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164424
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10401665
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182767
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854318
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182767
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182767
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001928	abnormal ovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182767
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182767
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21345181
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20160114	MGI			
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0002295	abnormal pulmonary circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12399445
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15581879
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16601074
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0003421	abnormal thyroid gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10401665
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0003421	abnormal thyroid gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21345181
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21345181
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182767
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0004551	decreased tracheal cartilage ring number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16601074
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0004733	abnormal thoracic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12399445
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854318
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16601074
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0005314	absent thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:21345181
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0005314	absent thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0005315	absent pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:21345181
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0005315	absent pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164424
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182767
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182767
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182767
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16601074
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010812	absent type II pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010814	absent alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164424
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164424
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010856	dilated respiratory conducting tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164424
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010911	abnormal pulmonary acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010943	abnormal bronchus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164424
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011034	impaired branching involved in respiratory bronchiole morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164424
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21345181
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164424
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0011145	abnormal mesenchymal cell differentiation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12829717
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0012684	abnormal pleural cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10208743
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0012684	abnormal pleural cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0013337	abnormal adenohypophysis development		IAGP		N	RGD:5509061	20141218	MGI			PMID:9806931
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0013351	abnormal Rathke's pouch development		IAGP		N	RGD:5509061	20141218	MGI			PMID:21345181
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0013351	abnormal Rathke's pouch development		IAGP		N	RGD:5509061	20141218	MGI			PMID:9806931
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0013352	abnormal Rathke's pouch apoptosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:9806931
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0013490	absent infundibular recess of third ventricle		IAGP		N	RGD:5509061	20150212	MGI			PMID:21345181
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0014198	absent pituitary infundibular stalk		IAGP		N	RGD:5509061	20160526	MGI			PMID:9806931
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:12399445
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0020556	abnormal ventromedial hypothalamic nucleus morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0020558	decreased ventromedial hypothalamic nucleus size		IAGP		N	RGD:5509061	20180315	MGI			PMID:8557195
11420	Nkx2-1	NK2 homeobox 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:17182767
11421	Tk1	thymidine kinase 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0003504	thyroid gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0003991	arteriosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0004035	abnormal sublingual gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0009161	pancreatic acinar cell zymogen granule accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0010138	arteritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10029690
11421	Tk1	thymidine kinase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12559842
11421	Tk1	thymidine kinase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10029690
11421	Tk1	thymidine kinase 1	gene	MP:0031071	lymph node atrophy		IAGP		N	RGD:5509061	20200618	MGI			PMID:12559842
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000492	abnormal rectum morphology		IEA		N	RGD:5509061	20210520	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210826	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20210128	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220519	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20231207	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0011816	decreased pre-pro B cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25153823
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
11422	Tle4	transducin-like enhancer of split 4	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:25153823
11425	Tmpo	thymopoietin	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849980
11425	Tmpo	thymopoietin	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849980
11425	Tmpo	thymopoietin	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849980
11425	Tmpo	thymopoietin	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849980
11425	Tmpo	thymopoietin	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849980
11425	Tmpo	thymopoietin	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849980
11425	Tmpo	thymopoietin	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849980
11429	Tnf	tumor necrosis factor	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20180719	MGI			PMID:17266397
11429	Tnf	tumor necrosis factor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17266397
11429	Tnf	tumor necrosis factor	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:16037568
11429	Tnf	tumor necrosis factor	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180719	MGI			PMID:15366373
11429	Tnf	tumor necrosis factor	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977323
11429	Tnf	tumor necrosis factor	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10878371
11429	Tnf	tumor necrosis factor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9177215
11429	Tnf	tumor necrosis factor	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:18299349
11429	Tnf	tumor necrosis factor	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10411942
11429	Tnf	tumor necrosis factor	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:18832037
11429	Tnf	tumor necrosis factor	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:23453632
11429	Tnf	tumor necrosis factor	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:10204494
11429	Tnf	tumor necrosis factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21436282
11429	Tnf	tumor necrosis factor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20180719	MGI			PMID:11063830
11429	Tnf	tumor necrosis factor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:11063830
11429	Tnf	tumor necrosis factor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180719	MGI			PMID:10411942
11429	Tnf	tumor necrosis factor	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20180719	MGI			PMID:11063830
11429	Tnf	tumor necrosis factor	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20180719	MGI			PMID:12163535
11429	Tnf	tumor necrosis factor	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20180719	MGI			PMID:10411942
11429	Tnf	tumor necrosis factor	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20180719	MGI			PMID:24727475
11429	Tnf	tumor necrosis factor	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:15664162
11429	Tnf	tumor necrosis factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:9223320
11429	Tnf	tumor necrosis factor	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20180719	MGI			PMID:18256672
11429	Tnf	tumor necrosis factor	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9223320
11429	Tnf	tumor necrosis factor	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:10204494
11429	Tnf	tumor necrosis factor	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:15334086
11429	Tnf	tumor necrosis factor	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:18439426
11429	Tnf	tumor necrosis factor	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:23453632
11429	Tnf	tumor necrosis factor	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:18439426
11429	Tnf	tumor necrosis factor	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:10395330
11429	Tnf	tumor necrosis factor	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20180719	MGI			PMID:16039576
11429	Tnf	tumor necrosis factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:10204494
11429	Tnf	tumor necrosis factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:15334086
11429	Tnf	tumor necrosis factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9177215
11429	Tnf	tumor necrosis factor	gene	MP:0002345	abnormal lymph node primary follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12115620
11429	Tnf	tumor necrosis factor	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0002363	abnormal spleen marginal sinus morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0002363	abnormal spleen marginal sinus morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9177215
11429	Tnf	tumor necrosis factor	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:15664162
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:15814712
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:16015367
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:8879212
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:9130661
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:9223320
11429	Tnf	tumor necrosis factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18439426
11429	Tnf	tumor necrosis factor	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20180719	MGI			PMID:18832037
11429	Tnf	tumor necrosis factor	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20180719	MGI			PMID:16037568
11429	Tnf	tumor necrosis factor	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20180719	MGI			PMID:11063830
11429	Tnf	tumor necrosis factor	gene	MP:0002791	steatorrhea		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:12727921
11429	Tnf	tumor necrosis factor	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:21804564
11429	Tnf	tumor necrosis factor	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20180719	MGI			PMID:15366373
11429	Tnf	tumor necrosis factor	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20180719	MGI			PMID:16287858
11429	Tnf	tumor necrosis factor	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20180719	MGI			PMID:18250193
11429	Tnf	tumor necrosis factor	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20180719	MGI			PMID:18439426
11429	Tnf	tumor necrosis factor	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:15334086
11429	Tnf	tumor necrosis factor	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:9223320
11429	Tnf	tumor necrosis factor	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20180719	MGI			PMID:11063830
11429	Tnf	tumor necrosis factor	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0003278	esophageal inflammation		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977323
11429	Tnf	tumor necrosis factor	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:10204494
11429	Tnf	tumor necrosis factor	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:15366373
11429	Tnf	tumor necrosis factor	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:18250193
11429	Tnf	tumor necrosis factor	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977323
11429	Tnf	tumor necrosis factor	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20180719	MGI			PMID:10204494
11429	Tnf	tumor necrosis factor	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20180719	MGI			PMID:24727475
11429	Tnf	tumor necrosis factor	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10639149
11429	Tnf	tumor necrosis factor	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20180719	MGI			PMID:18439426
11429	Tnf	tumor necrosis factor	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0004357	long tibia		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20180719	MGI			PMID:10395330
11429	Tnf	tumor necrosis factor	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:10064079
11429	Tnf	tumor necrosis factor	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:12471141
11429	Tnf	tumor necrosis factor	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9348316
11429	Tnf	tumor necrosis factor	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9565643
11429	Tnf	tumor necrosis factor	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:18832037
11429	Tnf	tumor necrosis factor	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18832037
11429	Tnf	tumor necrosis factor	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:17266397
11429	Tnf	tumor necrosis factor	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18250468
11429	Tnf	tumor necrosis factor	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18439426
11429	Tnf	tumor necrosis factor	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:9006341
11429	Tnf	tumor necrosis factor	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18256672
11429	Tnf	tumor necrosis factor	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20180719	MGI			PMID:18256672
11429	Tnf	tumor necrosis factor	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20180719	MGI			PMID:15334086
11429	Tnf	tumor necrosis factor	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20180719	MGI			PMID:10698075
11429	Tnf	tumor necrosis factor	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20180719	MGI			PMID:15664162
11429	Tnf	tumor necrosis factor	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:9223320
11429	Tnf	tumor necrosis factor	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18439426
11429	Tnf	tumor necrosis factor	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18854186
11429	Tnf	tumor necrosis factor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20180719	MGI			PMID:16037568
11429	Tnf	tumor necrosis factor	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20180719	MGI			PMID:8879212
11429	Tnf	tumor necrosis factor	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0005667	abnormal circulating leptin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0006167	eyelid edema		IAGP		N	RGD:5509061	20180719	MGI			PMID:23453632
11429	Tnf	tumor necrosis factor	gene	MP:0006278	aortic aneurysm		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:18854186
11429	Tnf	tumor necrosis factor	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:12486099
11429	Tnf	tumor necrosis factor	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977323
11429	Tnf	tumor necrosis factor	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20180719	MGI			PMID:9177215
11429	Tnf	tumor necrosis factor	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0008179	absent germinal center B cells		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0008197	abnormal follicular dendritic cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9223320
11429	Tnf	tumor necrosis factor	gene	MP:0008200	decreased follicular dendritic cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0008200	decreased follicular dendritic cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20180719	MGI			PMID:15832287
11429	Tnf	tumor necrosis factor	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20180719	MGI			PMID:9177215
11429	Tnf	tumor necrosis factor	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0008343	abnormal gamma-delta T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21419662
11429	Tnf	tumor necrosis factor	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:18439426
11429	Tnf	tumor necrosis factor	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:17218256
11429	Tnf	tumor necrosis factor	gene	MP:0008399	abnormal alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18439426
11429	Tnf	tumor necrosis factor	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20180719	MGI			PMID:10411942
11429	Tnf	tumor necrosis factor	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20180719	MGI			PMID:21436282
11429	Tnf	tumor necrosis factor	gene	MP:0008464	absent peripheral lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:12115620
11429	Tnf	tumor necrosis factor	gene	MP:0008471	abnormal spleen primary B follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0008471	abnormal spleen primary B follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0008471	abnormal spleen primary B follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0008471	abnormal spleen primary B follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8879212
11429	Tnf	tumor necrosis factor	gene	MP:0008471	abnormal spleen primary B follicle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9368616
11429	Tnf	tumor necrosis factor	gene	MP:0008473	abnormal spleen follicular dendritic cell network		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0008473	abnormal spleen follicular dendritic cell network		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0008473	abnormal spleen follicular dendritic cell network		IAGP		N	RGD:5509061	20180719	MGI			PMID:9287059
11429	Tnf	tumor necrosis factor	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20180719	MGI			PMID:16751399
11429	Tnf	tumor necrosis factor	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20180719	MGI			PMID:8879212
11429	Tnf	tumor necrosis factor	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20180719	MGI			PMID:9223320
11429	Tnf	tumor necrosis factor	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20180719	MGI			PMID:16705172
11429	Tnf	tumor necrosis factor	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:18256672
11429	Tnf	tumor necrosis factor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20180719	MGI			PMID:18256672
11429	Tnf	tumor necrosis factor	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20180719	MGI			PMID:21436282
11429	Tnf	tumor necrosis factor	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20180719	MGI			PMID:21436282
11429	Tnf	tumor necrosis factor	gene	MP:0008523	absent lymph node germinal center		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10204494
11429	Tnf	tumor necrosis factor	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977323
11429	Tnf	tumor necrosis factor	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180719	MGI			PMID:15664162
11429	Tnf	tumor necrosis factor	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:10204494
11429	Tnf	tumor necrosis factor	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:18854186
11429	Tnf	tumor necrosis factor	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:9130661
11429	Tnf	tumor necrosis factor	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:12727921
11429	Tnf	tumor necrosis factor	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:18250468
11429	Tnf	tumor necrosis factor	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:18256672
11429	Tnf	tumor necrosis factor	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0008639	decreased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:12727921
11429	Tnf	tumor necrosis factor	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:18854186
11429	Tnf	tumor necrosis factor	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:12727921
11429	Tnf	tumor necrosis factor	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12471141
11429	Tnf	tumor necrosis factor	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:15664162
11429	Tnf	tumor necrosis factor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180719	MGI			PMID:11672536
11429	Tnf	tumor necrosis factor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180719	MGI			PMID:15664162
11429	Tnf	tumor necrosis factor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180719	MGI			PMID:9130661
11429	Tnf	tumor necrosis factor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180719	MGI			PMID:9223320
11429	Tnf	tumor necrosis factor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180719	MGI			PMID:9426403
11429	Tnf	tumor necrosis factor	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180719	MGI			PMID:10204494
11429	Tnf	tumor necrosis factor	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20180719	MGI			PMID:12496444
11429	Tnf	tumor necrosis factor	gene	MP:0008852	retina neovascularization		IMP		N	RGD:7394795|PMID:19342600	20131105	RGD			
11429	Tnf	tumor necrosis factor	gene	MP:0008978	abnormal vagina weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:10453074
11429	Tnf	tumor necrosis factor	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20180719	MGI			PMID:10453074
11429	Tnf	tumor necrosis factor	gene	MP:0009384	cardiac valve regurgitation		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20180719	MGI			PMID:18299349
11429	Tnf	tumor necrosis factor	gene	MP:0009405	increased skeletal muscle fiber number		IAGP		N	RGD:5509061	20180719	MGI			PMID:18299349
11429	Tnf	tumor necrosis factor	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:21804564
11429	Tnf	tumor necrosis factor	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:16287858
11429	Tnf	tumor necrosis factor	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:18250468
11429	Tnf	tumor necrosis factor	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:18854186
11429	Tnf	tumor necrosis factor	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977323
11429	Tnf	tumor necrosis factor	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:10395330
11429	Tnf	tumor necrosis factor	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0009633	absent cervical lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:10586051
11429	Tnf	tumor necrosis factor	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20180719	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:10698075
11429	Tnf	tumor necrosis factor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:15664162
11429	Tnf	tumor necrosis factor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:16015367
11429	Tnf	tumor necrosis factor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180719	MGI			PMID:9834074
11429	Tnf	tumor necrosis factor	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:11063830
11429	Tnf	tumor necrosis factor	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0010170	abnormal glial cell apoptosis		IAGP		N	RGD:5509061	20251204	MGI			PMID:15905096
11429	Tnf	tumor necrosis factor	gene	MP:0010222	abnormal T-helper 17 cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0010360	decreased liver free fatty acids level		IAGP		N	RGD:5509061	20180719	MGI			PMID:16406654
11429	Tnf	tumor necrosis factor	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:16983719
11429	Tnf	tumor necrosis factor	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20231221	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0010620	thick mitral valve		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:18854186
11429	Tnf	tumor necrosis factor	gene	MP:0011079	decreased macrophage cytokine production		IEA		N	RGD:5509061	20180719	MGI			
11429	Tnf	tumor necrosis factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:19060883
11429	Tnf	tumor necrosis factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:12771125
11429	Tnf	tumor necrosis factor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0011572	abnormal aorta bulb morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0011709	increased fibroblast cell migration		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0011804	increased cell migration		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0011929	abnormal aortic valve flow		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0013147	limb paralysis		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:21804564
11429	Tnf	tumor necrosis factor	gene	MP:0014079	decreased small intestinal villus number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23977323
11429	Tnf	tumor necrosis factor	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:12446781
11429	Tnf	tumor necrosis factor	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:15664162
11429	Tnf	tumor necrosis factor	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:18832037
11429	Tnf	tumor necrosis factor	gene	MP:0014684	impaired spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:18832037
11429	Tnf	tumor necrosis factor	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:10204494
11429	Tnf	tumor necrosis factor	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0014897	increased circulating CCL20 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:23977107
11429	Tnf	tumor necrosis factor	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0020928	increased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:8671586
11429	Tnf	tumor necrosis factor	gene	MP:0030332	accelerated temporomandibular joint osteoarthritis		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0030466	alveolar process atrophy		IAGP		N	RGD:5509061	20180719	MGI			PMID:17305866
11429	Tnf	tumor necrosis factor	gene	MP:0030582	abnormal hair follicle placode formation		IAGP		N	RGD:5509061	20180719	MGI			PMID:15199130
11429	Tnf	tumor necrosis factor	gene	MP:0030795	joint dislocation		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0030814	abnormal wrist joint morphology		IAGP		N	RGD:5509061	20190117	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0031118	cardiovalvulitis		IAGP		N	RGD:5509061	20210826	MGI			PMID:33210082
11429	Tnf	tumor necrosis factor	gene	MP:0031118	cardiovalvulitis		IAGP		N	RGD:5509061	20240118	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0031124	aortic valve inflammation		IAGP		N	RGD:5509061	20200917	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0031124	aortic valve inflammation		IAGP		N	RGD:5509061	20240118	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0031516	mitral valve inflammation		IAGP		N	RGD:5509061	20240118	MGI			PMID:26195802
11429	Tnf	tumor necrosis factor	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:29618659
11429	Tnf	tumor necrosis factor	gene	MP:0031717	prolonged corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:29618659
11434	Tnnt2	troponin T2, cardiac	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556660
11434	Tnnt2	troponin T2, cardiac	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:18671960
11434	Tnnt2	troponin T2, cardiac	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556660
11434	Tnnt2	troponin T2, cardiac	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18671960
11434	Tnnt2	troponin T2, cardiac	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556660
11434	Tnnt2	troponin T2, cardiac	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18671960
11434	Tnnt2	troponin T2, cardiac	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18671960
11434	Tnnt2	troponin T2, cardiac	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556660
11434	Tnnt2	troponin T2, cardiac	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556660
11434	Tnnt2	troponin T2, cardiac	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0003822	decreased left ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556660
11434	Tnnt2	troponin T2, cardiac	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556660
11434	Tnnt2	troponin T2, cardiac	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:18671960
11434	Tnnt2	troponin T2, cardiac	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18671960
11434	Tnnt2	troponin T2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556660
11434	Tnnt2	troponin T2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18671960
11434	Tnnt2	troponin T2, cardiac	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18671960
11434	Tnnt2	troponin T2, cardiac	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17556660
11434	Tnnt2	troponin T2, cardiac	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0010553	prolonged HV interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18671960
11434	Tnnt2	troponin T2, cardiac	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612386
11434	Tnnt2	troponin T2, cardiac	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20171012	MGI			PMID:27936050
11434	Tnnt2	troponin T2, cardiac	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:17556660
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0000533	kidney hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11436	Tnnt3	troponin T3, skeletal, fast	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23775847
11437	Tnp1	transition protein 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10781074
11437	Tnp1	transition protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10781074
11437	Tnp1	transition protein 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10781074
11437	Tnp1	transition protein 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10781074
11437	Tnp1	transition protein 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10781074
11437	Tnp1	transition protein 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10781074
11437	Tnp1	transition protein 1	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10781074
11437	Tnp1	transition protein 1	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10781074
11438	Tnp2	transition protein 2	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685642
11438	Tnp2	transition protein 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685642
11438	Tnp2	transition protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385107
11438	Tnp2	transition protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685642
11438	Tnp2	transition protein 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585907
11438	Tnp2	transition protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385107
11438	Tnp2	transition protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585907
11438	Tnp2	transition protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12930723
11438	Tnp2	transition protein 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385107
11438	Tnp2	transition protein 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585907
11438	Tnp2	transition protein 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685642
11438	Tnp2	transition protein 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385107
11438	Tnp2	transition protein 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585907
11438	Tnp2	transition protein 2	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385107
11438	Tnp2	transition protein 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385107
11438	Tnp2	transition protein 2	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385107
11438	Tnp2	transition protein 2	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585907
11438	Tnp2	transition protein 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585907
11438	Tnp2	transition protein 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585907
11438	Tnp2	transition protein 2	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:11385107
11438	Tnp2	transition protein 2	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:15685642
11438	Tnp2	transition protein 2	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20191017	MGI			PMID:15685642
11438	Tnp2	transition protein 2	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20200227	MGI			PMID:15685642
11438	Tnp2	transition protein 2	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:11585907
11440	Trp53	transformation related protein 53	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706339
11440	Trp53	transformation related protein 53	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
11440	Trp53	transformation related protein 53	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
11440	Trp53	transformation related protein 53	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
11440	Trp53	transformation related protein 53	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
11440	Trp53	transformation related protein 53	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
11440	Trp53	transformation related protein 53	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790550
11440	Trp53	transformation related protein 53	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
11440	Trp53	transformation related protein 53	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654339
11440	Trp53	transformation related protein 53	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17070800
11440	Trp53	transformation related protein 53	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17251932
11440	Trp53	transformation related protein 53	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23798389
11440	Trp53	transformation related protein 53	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
11440	Trp53	transformation related protein 53	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533502
11440	Trp53	transformation related protein 53	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
11440	Trp53	transformation related protein 53	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11440	Trp53	transformation related protein 53	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7504233
11440	Trp53	transformation related protein 53	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16597604
11440	Trp53	transformation related protein 53	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
11440	Trp53	transformation related protein 53	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17070800
11440	Trp53	transformation related protein 53	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
11440	Trp53	transformation related protein 53	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
11440	Trp53	transformation related protein 53	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176372
11440	Trp53	transformation related protein 53	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228755
11440	Trp53	transformation related protein 53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
11440	Trp53	transformation related protein 53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17000755
11440	Trp53	transformation related protein 53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21487039
11440	Trp53	transformation related protein 53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
11440	Trp53	transformation related protein 53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382688
11440	Trp53	transformation related protein 53	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0000423	delayed hair regrowth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0000423	delayed hair regrowth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
11440	Trp53	transformation related protein 53	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
11440	Trp53	transformation related protein 53	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20190912	MGI			PMID:31197172
11440	Trp53	transformation related protein 53	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20210204	MGI			PMID:33110058
11440	Trp53	transformation related protein 53	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
11440	Trp53	transformation related protein 53	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
11440	Trp53	transformation related protein 53	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
11440	Trp53	transformation related protein 53	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
11440	Trp53	transformation related protein 53	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
11440	Trp53	transformation related protein 53	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
11440	Trp53	transformation related protein 53	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363841
11440	Trp53	transformation related protein 53	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363841
11440	Trp53	transformation related protein 53	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20200820	MGI			PMID:32728212
11440	Trp53	transformation related protein 53	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
11440	Trp53	transformation related protein 53	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34376666
11440	Trp53	transformation related protein 53	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11440	Trp53	transformation related protein 53	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
11440	Trp53	transformation related protein 53	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000569	abnormal digit pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20181227	MGI			PMID:18641651
11440	Trp53	transformation related protein 53	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
11440	Trp53	transformation related protein 53	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234449
11440	Trp53	transformation related protein 53	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:32381628
11440	Trp53	transformation related protein 53	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
11440	Trp53	transformation related protein 53	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:32381628
11440	Trp53	transformation related protein 53	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0000621	increased salivary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17212342
11440	Trp53	transformation related protein 53	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17212342
11440	Trp53	transformation related protein 53	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17996864
11440	Trp53	transformation related protein 53	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20220303	MGI			PMID:20585617
11440	Trp53	transformation related protein 53	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715125
11440	Trp53	transformation related protein 53	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
11440	Trp53	transformation related protein 53	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077642
11440	Trp53	transformation related protein 53	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077642
11440	Trp53	transformation related protein 53	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12555066
11440	Trp53	transformation related protein 53	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
11440	Trp53	transformation related protein 53	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268034
11440	Trp53	transformation related protein 53	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20170817	MGI			PMID:21804542
11440	Trp53	transformation related protein 53	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11440	Trp53	transformation related protein 53	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176372
11440	Trp53	transformation related protein 53	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
11440	Trp53	transformation related protein 53	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948956
11440	Trp53	transformation related protein 53	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20160804	MGI			PMID:24141783
11440	Trp53	transformation related protein 53	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20190912	MGI			PMID:31197172
11440	Trp53	transformation related protein 53	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:27815386
11440	Trp53	transformation related protein 53	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821748
11440	Trp53	transformation related protein 53	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
11440	Trp53	transformation related protein 53	gene	MP:0000865	absent cerebellum vermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821748
11440	Trp53	transformation related protein 53	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
11440	Trp53	transformation related protein 53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
11440	Trp53	transformation related protein 53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
11440	Trp53	transformation related protein 53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21127973
11440	Trp53	transformation related protein 53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
11440	Trp53	transformation related protein 53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:24209622
11440	Trp53	transformation related protein 53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171368
11440	Trp53	transformation related protein 53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
11440	Trp53	transformation related protein 53	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11914272
11440	Trp53	transformation related protein 53	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832489
11440	Trp53	transformation related protein 53	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
11440	Trp53	transformation related protein 53	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:24209622
11440	Trp53	transformation related protein 53	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208847
11440	Trp53	transformation related protein 53	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642502
11440	Trp53	transformation related protein 53	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342750
11440	Trp53	transformation related protein 53	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
11440	Trp53	transformation related protein 53	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
11440	Trp53	transformation related protein 53	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642502
11440	Trp53	transformation related protein 53	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
11440	Trp53	transformation related protein 53	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20585617
11440	Trp53	transformation related protein 53	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16288012
11440	Trp53	transformation related protein 53	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299132
11440	Trp53	transformation related protein 53	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22611036
11440	Trp53	transformation related protein 53	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
11440	Trp53	transformation related protein 53	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
11440	Trp53	transformation related protein 53	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11581300
11440	Trp53	transformation related protein 53	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15735727
11440	Trp53	transformation related protein 53	gene	MP:0001204	decreased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514395
11440	Trp53	transformation related protein 53	gene	MP:0001204	decreased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11581300
11440	Trp53	transformation related protein 53	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674344
11440	Trp53	transformation related protein 53	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502497
11440	Trp53	transformation related protein 53	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:28878021
11440	Trp53	transformation related protein 53	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:28878021
11440	Trp53	transformation related protein 53	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674344
11440	Trp53	transformation related protein 53	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190711	MGI			PMID:29635765
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210204	MGI			PMID:33110058
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11440	Trp53	transformation related protein 53	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22964582
11440	Trp53	transformation related protein 53	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20150924	MGI			PMID:25035393
11440	Trp53	transformation related protein 53	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17289567
11440	Trp53	transformation related protein 53	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12839925
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16288016
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397237
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585505
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17097565
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349585
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607363
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676052
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906694
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767771
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266220
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341455
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23486187
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23845441
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029233
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:24120138
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20150319	MGI			PMID:22617326
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20150514	MGI			PMID:24784840
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160204	MGI			PMID:25180607
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160804	MGI			PMID:24141783
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20170601	MGI			PMID:22190384
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20170608	MGI			PMID:24711431
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20170615	MGI			PMID:26411367
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20190516	MGI			PMID:28790031
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20190523	MGI			PMID:21282721
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11440	Trp53	transformation related protein 53	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956084
11440	Trp53	transformation related protein 53	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473278
11440	Trp53	transformation related protein 53	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20160204	MGI			PMID:25180607
11440	Trp53	transformation related protein 53	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
11440	Trp53	transformation related protein 53	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20180215	MGI			PMID:28294115
11440	Trp53	transformation related protein 53	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20210506	MGI			PMID:31794893
11440	Trp53	transformation related protein 53	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20240905	MGI			PMID:38733589
11440	Trp53	transformation related protein 53	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20250605	MGI			PMID:31048544
11440	Trp53	transformation related protein 53	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201022	MGI			
11440	Trp53	transformation related protein 53	gene	MP:0001296	macrophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484573
11440	Trp53	transformation related protein 53	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484573
11440	Trp53	transformation related protein 53	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20210204	MGI			PMID:33110058
11440	Trp53	transformation related protein 53	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10885750
11440	Trp53	transformation related protein 53	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484573
11440	Trp53	transformation related protein 53	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11440	Trp53	transformation related protein 53	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11440	Trp53	transformation related protein 53	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11440	Trp53	transformation related protein 53	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393064
11440	Trp53	transformation related protein 53	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11440	Trp53	transformation related protein 53	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804210
11440	Trp53	transformation related protein 53	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
11440	Trp53	transformation related protein 53	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17289567
11440	Trp53	transformation related protein 53	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
11440	Trp53	transformation related protein 53	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948956
11440	Trp53	transformation related protein 53	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11440	Trp53	transformation related protein 53	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0001396	unidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
11440	Trp53	transformation related protein 53	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
11440	Trp53	transformation related protein 53	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11440	Trp53	transformation related protein 53	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
11440	Trp53	transformation related protein 53	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11440	Trp53	transformation related protein 53	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:22964582
11440	Trp53	transformation related protein 53	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11440	Trp53	transformation related protein 53	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821748
11440	Trp53	transformation related protein 53	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334357
11440	Trp53	transformation related protein 53	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20362536
11440	Trp53	transformation related protein 53	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20170615	MGI			PMID:26411367
11440	Trp53	transformation related protein 53	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
11440	Trp53	transformation related protein 53	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332968
11440	Trp53	transformation related protein 53	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334357
11440	Trp53	transformation related protein 53	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14702042
11440	Trp53	transformation related protein 53	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15081359
11440	Trp53	transformation related protein 53	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11440	Trp53	transformation related protein 53	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20150129	MGI			PMID:24706806
11440	Trp53	transformation related protein 53	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779492
11440	Trp53	transformation related protein 53	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20210506	MGI			PMID:31794893
11440	Trp53	transformation related protein 53	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
11440	Trp53	transformation related protein 53	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
11440	Trp53	transformation related protein 53	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17289567
11440	Trp53	transformation related protein 53	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
11440	Trp53	transformation related protein 53	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
11440	Trp53	transformation related protein 53	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
11440	Trp53	transformation related protein 53	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10191063
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980714
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832489
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790550
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22579044
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207798
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872327
11440	Trp53	transformation related protein 53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
11440	Trp53	transformation related protein 53	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
11440	Trp53	transformation related protein 53	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20150129	MGI			PMID:24706806
11440	Trp53	transformation related protein 53	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207798
11440	Trp53	transformation related protein 53	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
11440	Trp53	transformation related protein 53	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207798
11440	Trp53	transformation related protein 53	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10191063
11440	Trp53	transformation related protein 53	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17000755
11440	Trp53	transformation related protein 53	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858271
11440	Trp53	transformation related protein 53	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10786799
11440	Trp53	transformation related protein 53	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11440	Trp53	transformation related protein 53	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20210617	MGI			PMID:28747430
11440	Trp53	transformation related protein 53	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
11440	Trp53	transformation related protein 53	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
11440	Trp53	transformation related protein 53	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414647
11440	Trp53	transformation related protein 53	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20190711	MGI			PMID:29635765
11440	Trp53	transformation related protein 53	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20190711	MGI			PMID:29635765
11440	Trp53	transformation related protein 53	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22964582
11440	Trp53	transformation related protein 53	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20190711	MGI			PMID:29635765
11440	Trp53	transformation related protein 53	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18304521
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694875
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15131084
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150107
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715125
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17097565
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510390
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21324922
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20150514	MGI			PMID:24784840
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20160331	MGI			PMID:25330770
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20160428	MGI			PMID:16166291
11440	Trp53	transformation related protein 53	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20190523	MGI			PMID:21282721
11440	Trp53	transformation related protein 53	gene	MP:0001884	mammary gland alveolar hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17653086
11440	Trp53	transformation related protein 53	gene	MP:0001885	mammary gland duct hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715125
11440	Trp53	transformation related protein 53	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851974
11440	Trp53	transformation related protein 53	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20111116	MGI			
11440	Trp53	transformation related protein 53	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
11440	Trp53	transformation related protein 53	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
11440	Trp53	transformation related protein 53	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
11440	Trp53	transformation related protein 53	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20170608	MGI			PMID:24711431
11440	Trp53	transformation related protein 53	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077642
11440	Trp53	transformation related protein 53	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12555066
11440	Trp53	transformation related protein 53	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22964582
11440	Trp53	transformation related protein 53	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20150924	MGI			PMID:25035393
11440	Trp53	transformation related protein 53	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0002009	preneoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17653086
11440	Trp53	transformation related protein 53	gene	MP:0002013	increased pilomatricoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17097565
11440	Trp53	transformation related protein 53	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574128
11440	Trp53	transformation related protein 53	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23741457
11440	Trp53	transformation related protein 53	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414647
11440	Trp53	transformation related protein 53	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
11440	Trp53	transformation related protein 53	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21056012
11440	Trp53	transformation related protein 53	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20180809	MGI			PMID:11159909
11440	Trp53	transformation related protein 53	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
11440	Trp53	transformation related protein 53	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
11440	Trp53	transformation related protein 53	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
11440	Trp53	transformation related protein 53	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20201224	MGI			PMID:31483066
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077642
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346812
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11169961
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11280729
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323676
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544182
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694875
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12096340
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414647
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432262
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647411
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14702042
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15131084
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150107
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1552940
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821748
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767157
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16785989
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158963
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906694
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199537
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251665
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19881536
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552324
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239359
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7504233
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8048955
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20170314	MGI			PMID:27815386
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
11440	Trp53	transformation related protein 53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
11440	Trp53	transformation related protein 53	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914701
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10786799
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343266
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775323
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349429
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552324
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689981
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20201224	MGI			PMID:31483066
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20260312	MGI			PMID:34406363
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077642
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323676
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208847
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12555066
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647411
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14702042
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706337
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15131084
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15924142
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473278
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17984302
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775323
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19126872
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767771
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21324922
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349429
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685933
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7504233
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584189
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20180906	MGI			PMID:25565005
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20201224	MGI			PMID:31483066
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20211021	MGI			PMID:28076792
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906694
11440	Trp53	transformation related protein 53	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19332766
11440	Trp53	transformation related protein 53	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20180906	MGI			PMID:25565005
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16288016
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299132
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19765830
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19847165
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228755
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22611036
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22964582
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23285300
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23565506
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20150924	MGI			PMID:25035393
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20171116	MGI			PMID:11751631
11440	Trp53	transformation related protein 53	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
11440	Trp53	transformation related protein 53	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
11440	Trp53	transformation related protein 53	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397217
11440	Trp53	transformation related protein 53	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242513
11440	Trp53	transformation related protein 53	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11169961
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647411
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14702042
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343266
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1552940
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674344
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821748
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676052
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19881536
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956606
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21056012
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512139
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552324
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228755
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22293175
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24115439
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239359
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:9861017
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20160428	MGI			PMID:16166291
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20201224	MGI			PMID:31483066
11440	Trp53	transformation related protein 53	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0002033	increased malignant triton tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11440	Trp53	transformation related protein 53	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20211021	MGI			PMID:28076792
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706339
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489287
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16785989
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:9861017
11440	Trp53	transformation related protein 53	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20211021	MGI			PMID:28076792
11440	Trp53	transformation related protein 53	gene	MP:0002037	increased fibrohistocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079851
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363841
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607363
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176372
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19261747
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21331045
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502497
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574128
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:9861017
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20150319	MGI			PMID:22617326
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20201224	MGI			PMID:31483066
11440	Trp53	transformation related protein 53	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9214616
11440	Trp53	transformation related protein 53	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
11440	Trp53	transformation related protein 53	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11440	Trp53	transformation related protein 53	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029233
11440	Trp53	transformation related protein 53	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20200820	MGI			PMID:32728212
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16288016
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411819
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23285300
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239348
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20151112	MGI			PMID:22606359
11440	Trp53	transformation related protein 53	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
11440	Trp53	transformation related protein 53	gene	MP:0002049	increased extremity angiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323676
11440	Trp53	transformation related protein 53	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456863
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729946
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319471
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397217
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767157
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24209622
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584189
11440	Trp53	transformation related protein 53	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
11440	Trp53	transformation related protein 53	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19847165
11440	Trp53	transformation related protein 53	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674344
11440	Trp53	transformation related protein 53	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
11440	Trp53	transformation related protein 53	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948956
11440	Trp53	transformation related protein 53	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171368
11440	Trp53	transformation related protein 53	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11440	Trp53	transformation related protein 53	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936560
11440	Trp53	transformation related protein 53	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077642
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591652
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10757812
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10786799
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323676
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544182
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967151
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208847
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12234974
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12555066
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670909
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914701
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706337
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15131084
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343266
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:1552940
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674344
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079851
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16288016
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397237
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158963
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349585
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967868
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632614
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19126872
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176372
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19261747
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633665
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767771
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19881536
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20406986
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21056012
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21324922
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21331045
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625383
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232209
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266220
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341455
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411819
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22611036
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689981
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23486187
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24115439
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584189
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141225	MGI			PMID:24652652
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150507	MGI			PMID:23851502
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150514	MGI			PMID:24784840
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150924	MGI			PMID:25035393
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160324	MGI			PMID:12426394
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160428	MGI			PMID:16166291
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20161013	MGI			PMID:26659571
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170601	MGI			PMID:22190384
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170608	MGI			PMID:24711431
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170615	MGI			PMID:26411367
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190131	MGI			PMID:28934293
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190516	MGI			PMID:28790031
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190711	MGI			PMID:29635765
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191205	MGI			PMID:31685994
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201224	MGI			PMID:31483066
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230601	MGI			PMID:30093633
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230615	MGI			PMID:34803166
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
11440	Trp53	transformation related protein 53	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884603
11440	Trp53	transformation related protein 53	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
11440	Trp53	transformation related protein 53	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171368
11440	Trp53	transformation related protein 53	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872327
11440	Trp53	transformation related protein 53	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
11440	Trp53	transformation related protein 53	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11440	Trp53	transformation related protein 53	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11440	Trp53	transformation related protein 53	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24706806
11440	Trp53	transformation related protein 53	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17129780
11440	Trp53	transformation related protein 53	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694875
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17289567
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998932
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19556538
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730163
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477326
11440	Trp53	transformation related protein 53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477327
11440	Trp53	transformation related protein 53	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411819
11440	Trp53	transformation related protein 53	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20181227	MGI			PMID:18641651
11440	Trp53	transformation related protein 53	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:29635765
11440	Trp53	transformation related protein 53	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
11440	Trp53	transformation related protein 53	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
11440	Trp53	transformation related protein 53	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10786799
11440	Trp53	transformation related protein 53	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200820	MGI			PMID:32728212
11440	Trp53	transformation related protein 53	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473278
11440	Trp53	transformation related protein 53	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473278
11440	Trp53	transformation related protein 53	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
11440	Trp53	transformation related protein 53	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
11440	Trp53	transformation related protein 53	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346812
11440	Trp53	transformation related protein 53	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967151
11440	Trp53	transformation related protein 53	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
11440	Trp53	transformation related protein 53	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11440	Trp53	transformation related protein 53	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24115439
11440	Trp53	transformation related protein 53	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
11440	Trp53	transformation related protein 53	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
11440	Trp53	transformation related protein 53	gene	MP:0002661	abnormal corpus epididymis morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:22678923
11440	Trp53	transformation related protein 53	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858271
11440	Trp53	transformation related protein 53	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
11440	Trp53	transformation related protein 53	gene	MP:0002700	increased opacity of vitreous body		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393064
11440	Trp53	transformation related protein 53	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11440	Trp53	transformation related protein 53	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21831840
11440	Trp53	transformation related protein 53	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393064
11440	Trp53	transformation related protein 53	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10885750
11440	Trp53	transformation related protein 53	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393064
11440	Trp53	transformation related protein 53	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
11440	Trp53	transformation related protein 53	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
11440	Trp53	transformation related protein 53	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510390
11440	Trp53	transformation related protein 53	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11440	Trp53	transformation related protein 53	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20150514	MGI			PMID:24784840
11440	Trp53	transformation related protein 53	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0003010	decreased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
11440	Trp53	transformation related protein 53	gene	MP:0003010	decreased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0003010	decreased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
11440	Trp53	transformation related protein 53	gene	MP:0003046	liver cirrhosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
11440	Trp53	transformation related protein 53	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
11440	Trp53	transformation related protein 53	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973245
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654339
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16006521
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158931
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160036
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216268
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21127973
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9472983
11440	Trp53	transformation related protein 53	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11440	Trp53	transformation related protein 53	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21831840
11440	Trp53	transformation related protein 53	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
11440	Trp53	transformation related protein 53	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
11440	Trp53	transformation related protein 53	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
11440	Trp53	transformation related protein 53	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11150333
11440	Trp53	transformation related protein 53	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973245
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097646
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192050
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343266
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15924142
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158931
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779492
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565614
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20220922	MGI			PMID:27668660
11440	Trp53	transformation related protein 53	gene	MP:0003223	decreased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
11440	Trp53	transformation related protein 53	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
11440	Trp53	transformation related protein 53	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17129780
11440	Trp53	transformation related protein 53	gene	MP:0003269	colon polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0003269	colon polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
11440	Trp53	transformation related protein 53	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0003277	increased esophageal papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0003299	gastric polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0003299	gastric polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
11440	Trp53	transformation related protein 53	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20190711	MGI			PMID:29635765
11440	Trp53	transformation related protein 53	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234449
11440	Trp53	transformation related protein 53	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
11440	Trp53	transformation related protein 53	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397237
11440	Trp53	transformation related protein 53	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234449
11440	Trp53	transformation related protein 53	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029233
11440	Trp53	transformation related protein 53	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
11440	Trp53	transformation related protein 53	gene	MP:0003335	exocrine pancreatic insufficiency		IAGP		N	RGD:5509061	20141003	MGI			PMID:21056012
11440	Trp53	transformation related protein 53	gene	MP:0003365	increased glucagonoma incidence		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11440	Trp53	transformation related protein 53	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
11440	Trp53	transformation related protein 53	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19847165
11440	Trp53	transformation related protein 53	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341455
11440	Trp53	transformation related protein 53	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20191205	MGI			PMID:31685994
11440	Trp53	transformation related protein 53	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11440	Trp53	transformation related protein 53	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12096340
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607363
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176372
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19847165
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22172724
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:35700263
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
11440	Trp53	transformation related protein 53	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20260312	MGI			PMID:34406363
11440	Trp53	transformation related protein 53	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20161222	MGI			PMID:27354067
11440	Trp53	transformation related protein 53	gene	MP:0003570	increased uterus leiomyoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0003574	abnormal oviduct morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:22617326
11440	Trp53	transformation related protein 53	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12839925
11440	Trp53	transformation related protein 53	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20150319	MGI			PMID:22617326
11440	Trp53	transformation related protein 53	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
11440	Trp53	transformation related protein 53	gene	MP:0003587	ureter obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17653086
11440	Trp53	transformation related protein 53	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079851
11440	Trp53	transformation related protein 53	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20585617
11440	Trp53	transformation related protein 53	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
11440	Trp53	transformation related protein 53	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077642
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346812
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323676
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1552940
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20587514
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552324
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:9861017
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
11440	Trp53	transformation related protein 53	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20211021	MGI			PMID:28076792
11440	Trp53	transformation related protein 53	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
11440	Trp53	transformation related protein 53	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
11440	Trp53	transformation related protein 53	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414647
11440	Trp53	transformation related protein 53	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
11440	Trp53	transformation related protein 53	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
11440	Trp53	transformation related protein 53	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341455
11440	Trp53	transformation related protein 53	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22579044
11440	Trp53	transformation related protein 53	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
11440	Trp53	transformation related protein 53	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11440	Trp53	transformation related protein 53	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
11440	Trp53	transformation related protein 53	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625383
11440	Trp53	transformation related protein 53	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228755
11440	Trp53	transformation related protein 53	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
11440	Trp53	transformation related protein 53	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20210506	MGI			PMID:31794893
11440	Trp53	transformation related protein 53	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20230601	MGI			PMID:30093633
11440	Trp53	transformation related protein 53	gene	MP:0003750	increased mouth tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
11440	Trp53	transformation related protein 53	gene	MP:0003750	increased mouth tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029233
11440	Trp53	transformation related protein 53	gene	MP:0003751	oral leukoplakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
11440	Trp53	transformation related protein 53	gene	MP:0003751	oral leukoplakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19881536
11440	Trp53	transformation related protein 53	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21127973
11440	Trp53	transformation related protein 53	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414647
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1552940
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546942
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559481
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20587514
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23486187
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:9861017
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20160804	MGI			PMID:24141783
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20161013	MGI			PMID:26659571
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:26360410
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:29743593
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:30093633
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:35700263
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:36073547
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11440	Trp53	transformation related protein 53	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
11440	Trp53	transformation related protein 53	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:32381628
11440	Trp53	transformation related protein 53	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20210422	MGI			PMID:32381628
11440	Trp53	transformation related protein 53	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0003927	increased cellular glucose import		IAGP		N	RGD:5509061	20141003	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
11440	Trp53	transformation related protein 53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11440	Trp53	transformation related protein 53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
11440	Trp53	transformation related protein 53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
11440	Trp53	transformation related protein 53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
11440	Trp53	transformation related protein 53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
11440	Trp53	transformation related protein 53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22579044
11440	Trp53	transformation related protein 53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171368
11440	Trp53	transformation related protein 53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207798
11440	Trp53	transformation related protein 53	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508513
11440	Trp53	transformation related protein 53	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17251932
11440	Trp53	transformation related protein 53	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872327
11440	Trp53	transformation related protein 53	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14702042
11440	Trp53	transformation related protein 53	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767157
11440	Trp53	transformation related protein 53	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
11440	Trp53	transformation related protein 53	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20190912	MGI			PMID:31197172
11440	Trp53	transformation related protein 53	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20210211	MGI			PMID:31662330
11440	Trp53	transformation related protein 53	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11440	Trp53	transformation related protein 53	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715125
11440	Trp53	transformation related protein 53	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832489
11440	Trp53	transformation related protein 53	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
11440	Trp53	transformation related protein 53	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10881179
11440	Trp53	transformation related protein 53	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713479
11440	Trp53	transformation related protein 53	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19126872
11440	Trp53	transformation related protein 53	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872327
11440	Trp53	transformation related protein 53	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677503
11440	Trp53	transformation related protein 53	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431698
11440	Trp53	transformation related protein 53	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097646
11440	Trp53	transformation related protein 53	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
11440	Trp53	transformation related protein 53	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192050
11440	Trp53	transformation related protein 53	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654339
11440	Trp53	transformation related protein 53	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19881536
11440	Trp53	transformation related protein 53	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20150129	MGI			PMID:24706806
11440	Trp53	transformation related protein 53	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20210204	MGI			PMID:33110058
11440	Trp53	transformation related protein 53	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
11440	Trp53	transformation related protein 53	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181534
11440	Trp53	transformation related protein 53	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207798
11440	Trp53	transformation related protein 53	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20180503	MGI			PMID:29358667
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17097565
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607363
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176372
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:9861017
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20150514	MGI			PMID:24784840
11440	Trp53	transformation related protein 53	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20211021	MGI			PMID:28076792
11440	Trp53	transformation related protein 53	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20180913	MGI			PMID:24162662
11440	Trp53	transformation related protein 53	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
11440	Trp53	transformation related protein 53	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943427
11440	Trp53	transformation related protein 53	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17122775
11440	Trp53	transformation related protein 53	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
11440	Trp53	transformation related protein 53	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713479
11440	Trp53	transformation related protein 53	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20587514
11440	Trp53	transformation related protein 53	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514395
11440	Trp53	transformation related protein 53	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414647
11440	Trp53	transformation related protein 53	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12909629
11440	Trp53	transformation related protein 53	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729946
11440	Trp53	transformation related protein 53	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
11440	Trp53	transformation related protein 53	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20587514
11440	Trp53	transformation related protein 53	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21127973
11440	Trp53	transformation related protein 53	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24706806
11440	Trp53	transformation related protein 53	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0004390	abnormal bronchoalveolar duct junction morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411819
11440	Trp53	transformation related protein 53	gene	MP:0004478	increased testicular teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11440	Trp53	transformation related protein 53	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651430
11440	Trp53	transformation related protein 53	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363841
11440	Trp53	transformation related protein 53	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607363
11440	Trp53	transformation related protein 53	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21151170
11440	Trp53	transformation related protein 53	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20160428	MGI			PMID:16166291
11440	Trp53	transformation related protein 53	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20181129	MGI			PMID:30042151
11440	Trp53	transformation related protein 53	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779492
11440	Trp53	transformation related protein 53	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
11440	Trp53	transformation related protein 53	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
11440	Trp53	transformation related protein 53	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
11440	Trp53	transformation related protein 53	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20150827	MGI			PMID:20718941
11440	Trp53	transformation related protein 53	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12566297
11440	Trp53	transformation related protein 53	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314658
11440	Trp53	transformation related protein 53	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607363
11440	Trp53	transformation related protein 53	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16785989
11440	Trp53	transformation related protein 53	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
11440	Trp53	transformation related protein 53	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
11440	Trp53	transformation related protein 53	gene	MP:0004684	intervertebral disk degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17996864
11440	Trp53	transformation related protein 53	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
11440	Trp53	transformation related protein 53	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
11440	Trp53	transformation related protein 53	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
11440	Trp53	transformation related protein 53	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713479
11440	Trp53	transformation related protein 53	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
11440	Trp53	transformation related protein 53	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
11440	Trp53	transformation related protein 53	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
11440	Trp53	transformation related protein 53	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632614
11440	Trp53	transformation related protein 53	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141204	MGI			PMID:22678923
11440	Trp53	transformation related protein 53	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141204	MGI			PMID:24930886
11440	Trp53	transformation related protein 53	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:22678923
11440	Trp53	transformation related protein 53	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632614
11440	Trp53	transformation related protein 53	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
11440	Trp53	transformation related protein 53	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
11440	Trp53	transformation related protein 53	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
11440	Trp53	transformation related protein 53	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
11440	Trp53	transformation related protein 53	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0005134	decreased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20170601	MGI			PMID:22190384
11440	Trp53	transformation related protein 53	gene	MP:0005135	increased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20170608	MGI			PMID:24711431
11440	Trp53	transformation related protein 53	gene	MP:0005141	liver hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
11440	Trp53	transformation related protein 53	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642502
11440	Trp53	transformation related protein 53	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232209
11440	Trp53	transformation related protein 53	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642502
11440	Trp53	transformation related protein 53	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20170615	MGI			PMID:26411367
11440	Trp53	transformation related protein 53	gene	MP:0005195	abnormal posterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393064
11440	Trp53	transformation related protein 53	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11440	Trp53	transformation related protein 53	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7478622
11440	Trp53	transformation related protein 53	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0005299	abnormal eye posterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11440	Trp53	transformation related protein 53	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
11440	Trp53	transformation related protein 53	gene	MP:0005355	enlarged thyroid gland		IAGP		N	RGD:5509061	20170601	MGI			PMID:22190384
11440	Trp53	transformation related protein 53	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432262
11440	Trp53	transformation related protein 53	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20181227	MGI			PMID:18641651
11440	Trp53	transformation related protein 53	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266220
11440	Trp53	transformation related protein 53	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0005488	bronchial epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11440	Trp53	transformation related protein 53	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11440	Trp53	transformation related protein 53	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570515
11440	Trp53	transformation related protein 53	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
11440	Trp53	transformation related protein 53	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
11440	Trp53	transformation related protein 53	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334357
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508513
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16597604
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172844
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21831840
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23798389
11440	Trp53	transformation related protein 53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20210204	MGI			PMID:33110058
11440	Trp53	transformation related protein 53	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20210617	MGI			PMID:28747430
11440	Trp53	transformation related protein 53	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:28747430
11440	Trp53	transformation related protein 53	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
11440	Trp53	transformation related protein 53	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859164
11440	Trp53	transformation related protein 53	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
11440	Trp53	transformation related protein 53	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21331045
11440	Trp53	transformation related protein 53	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:31197172
11440	Trp53	transformation related protein 53	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11150333
11440	Trp53	transformation related protein 53	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11440	Trp53	transformation related protein 53	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
11440	Trp53	transformation related protein 53	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158931
11440	Trp53	transformation related protein 53	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
11440	Trp53	transformation related protein 53	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565614
11440	Trp53	transformation related protein 53	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
11440	Trp53	transformation related protein 53	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076674
11440	Trp53	transformation related protein 53	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0006206	embryonic lethality between somite formation and embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10567591
11440	Trp53	transformation related protein 53	gene	MP:0006219	optic nerve degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393064
11440	Trp53	transformation related protein 53	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393064
11440	Trp53	transformation related protein 53	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20201224	MGI			PMID:31483066
11440	Trp53	transformation related protein 53	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20190523	MGI			PMID:21282721
11440	Trp53	transformation related protein 53	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10783170
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260494
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775323
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213072
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633665
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343890
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574128
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22722829
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24115439
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:9861017
11440	Trp53	transformation related protein 53	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20170314	MGI			PMID:27815386
11440	Trp53	transformation related protein 53	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0006310	increased retinoblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
11440	Trp53	transformation related protein 53	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12839925
11440	Trp53	transformation related protein 53	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
11440	Trp53	transformation related protein 53	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20150319	MGI			PMID:22617326
11440	Trp53	transformation related protein 53	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20161222	MGI			PMID:27354067
11440	Trp53	transformation related protein 53	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216268
11440	Trp53	transformation related protein 53	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570515
11440	Trp53	transformation related protein 53	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21831840
11440	Trp53	transformation related protein 53	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21127973
11440	Trp53	transformation related protein 53	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228755
11440	Trp53	transformation related protein 53	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0008010	increased gastric adenocarcinoma incidence		IAGP		N	RGD:5509061	20150514	MGI			PMID:24784840
11440	Trp53	transformation related protein 53	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16288016
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299132
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19765830
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20406986
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22964582
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20150924	MGI			PMID:25035393
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20160428	MGI			PMID:16166291
11440	Trp53	transformation related protein 53	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20171116	MGI			PMID:11751631
11440	Trp53	transformation related protein 53	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
11440	Trp53	transformation related protein 53	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
11440	Trp53	transformation related protein 53	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029233
11440	Trp53	transformation related protein 53	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24120138
11440	Trp53	transformation related protein 53	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23207905
11440	Trp53	transformation related protein 53	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779492
11440	Trp53	transformation related protein 53	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
11440	Trp53	transformation related protein 53	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20151001	MGI			PMID:25201955
11440	Trp53	transformation related protein 53	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
11440	Trp53	transformation related protein 53	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
11440	Trp53	transformation related protein 53	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642502
11440	Trp53	transformation related protein 53	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
11440	Trp53	transformation related protein 53	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0008402	increased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22579044
11440	Trp53	transformation related protein 53	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20587514
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12909629
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12952892
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456863
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654339
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510390
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216268
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20587514
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21127973
11440	Trp53	transformation related protein 53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21487039
11440	Trp53	transformation related protein 53	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
11440	Trp53	transformation related protein 53	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20210617	MGI			PMID:28747430
11440	Trp53	transformation related protein 53	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
11440	Trp53	transformation related protein 53	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
11440	Trp53	transformation related protein 53	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11440	Trp53	transformation related protein 53	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
11440	Trp53	transformation related protein 53	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
11440	Trp53	transformation related protein 53	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0008623	increased circulating interleukin-3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20170615	MGI			PMID:26411367
11440	Trp53	transformation related protein 53	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11440	Trp53	transformation related protein 53	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19765830
11440	Trp53	transformation related protein 53	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20406986
11440	Trp53	transformation related protein 53	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22611036
11440	Trp53	transformation related protein 53	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11440	Trp53	transformation related protein 53	gene	MP:0008715	increased lung small cell carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11440	Trp53	transformation related protein 53	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22611036
11440	Trp53	transformation related protein 53	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22964582
11440	Trp53	transformation related protein 53	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23207905
11440	Trp53	transformation related protein 53	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21966279
11440	Trp53	transformation related protein 53	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546942
11440	Trp53	transformation related protein 53	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19126872
11440	Trp53	transformation related protein 53	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0008780	increased pancreatic acinar cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0008780	increased pancreatic acinar cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16169464
11440	Trp53	transformation related protein 53	gene	MP:0008780	increased pancreatic acinar cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21056012
11440	Trp53	transformation related protein 53	gene	MP:0008780	increased pancreatic acinar cell carcinoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:7478622
11440	Trp53	transformation related protein 53	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0008830	abnormal nucleolus morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:35139074
11440	Trp53	transformation related protein 53	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:10881179
11440	Trp53	transformation related protein 53	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19881536
11440	Trp53	transformation related protein 53	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11440	Trp53	transformation related protein 53	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:22579044
11440	Trp53	transformation related protein 53	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
11440	Trp53	transformation related protein 53	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
11440	Trp53	transformation related protein 53	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21331045
11440	Trp53	transformation related protein 53	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20200820	MGI			PMID:32728212
11440	Trp53	transformation related protein 53	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0008891	decreased hepatocyte apoptosis		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
11440	Trp53	transformation related protein 53	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12952892
11440	Trp53	transformation related protein 53	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779492
11440	Trp53	transformation related protein 53	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:10508513
11440	Trp53	transformation related protein 53	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:12097646
11440	Trp53	transformation related protein 53	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:17158931
11440	Trp53	transformation related protein 53	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
11440	Trp53	transformation related protein 53	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
11440	Trp53	transformation related protein 53	gene	MP:0009004	progressive hair loss		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632614
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16169464
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585505
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349585
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21056012
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232209
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453624
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20150528	MGI			PMID:25878147
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20150827	MGI			PMID:22541435
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20180809	MGI			PMID:11159909
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20190131	MGI			PMID:28934293
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20190516	MGI			PMID:28790031
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20191205	MGI			PMID:31685994
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
11440	Trp53	transformation related protein 53	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
11440	Trp53	transformation related protein 53	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232209
11440	Trp53	transformation related protein 53	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20190131	MGI			PMID:28934293
11440	Trp53	transformation related protein 53	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20190516	MGI			PMID:28790031
11440	Trp53	transformation related protein 53	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20191205	MGI			PMID:31685994
11440	Trp53	transformation related protein 53	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
11440	Trp53	transformation related protein 53	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585505
11440	Trp53	transformation related protein 53	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20170615	MGI			PMID:26411367
11440	Trp53	transformation related protein 53	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20180809	MGI			PMID:11159909
11440	Trp53	transformation related protein 53	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
11440	Trp53	transformation related protein 53	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20585617
11440	Trp53	transformation related protein 53	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341455
11440	Trp53	transformation related protein 53	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341455
11440	Trp53	transformation related protein 53	gene	MP:0009258	abnormal thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12909629
11440	Trp53	transformation related protein 53	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
11440	Trp53	transformation related protein 53	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652750
11440	Trp53	transformation related protein 53	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
11440	Trp53	transformation related protein 53	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20170314	MGI			PMID:27815386
11440	Trp53	transformation related protein 53	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16288016
11440	Trp53	transformation related protein 53	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411819
11440	Trp53	transformation related protein 53	gene	MP:0009309	increased small intestine adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0009311	increased duodenum adenocarcinoma incidence		IAGP		N	RGD:5509061	20150514	MGI			PMID:24784840
11440	Trp53	transformation related protein 53	gene	MP:0009314	increased colon adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
11440	Trp53	transformation related protein 53	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779492
11440	Trp53	transformation related protein 53	gene	MP:0009318	increased splenic marginal zone lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
11440	Trp53	transformation related protein 53	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20211021	MGI			PMID:28076792
11440	Trp53	transformation related protein 53	gene	MP:0009332	abnormal splenocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0009341	decreased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0009442	increased ovarian teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23741457
11440	Trp53	transformation related protein 53	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20190523	MGI			PMID:21282721
11440	Trp53	transformation related protein 53	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715125
11440	Trp53	transformation related protein 53	gene	MP:0009505	abnormal mammary gland lobule morphology		IAGP		N	RGD:5509061	20190523	MGI			PMID:21282721
11440	Trp53	transformation related protein 53	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0009508	increased mammary gland ductal carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17212342
11440	Trp53	transformation related protein 53	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172844
11440	Trp53	transformation related protein 53	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677503
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19881536
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20362536
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23166633
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23207905
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20160324	MGI			PMID:12426394
11440	Trp53	transformation related protein 53	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19261747
11440	Trp53	transformation related protein 53	gene	MP:0009551	increased urinary bladder transitional cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
11440	Trp53	transformation related protein 53	gene	MP:0009552	urinary bladder obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079851
11440	Trp53	transformation related protein 53	gene	MP:0009566	meiotic nondisjunction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642502
11440	Trp53	transformation related protein 53	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176372
11440	Trp53	transformation related protein 53	gene	MP:0009591	increased liver adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0009591	increased liver adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0009600	hypergranulosis		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0009625	abnormal abdominal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
11440	Trp53	transformation related protein 53	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
11440	Trp53	transformation related protein 53	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502497
11440	Trp53	transformation related protein 53	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20180913	MGI			PMID:24162662
11440	Trp53	transformation related protein 53	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533502
11440	Trp53	transformation related protein 53	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363841
11440	Trp53	transformation related protein 53	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858271
11440	Trp53	transformation related protein 53	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150107
11440	Trp53	transformation related protein 53	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
11440	Trp53	transformation related protein 53	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
11440	Trp53	transformation related protein 53	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22034435
11440	Trp53	transformation related protein 53	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22172724
11440	Trp53	transformation related protein 53	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11440	Trp53	transformation related protein 53	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260494
11440	Trp53	transformation related protein 53	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633665
11440	Trp53	transformation related protein 53	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
11440	Trp53	transformation related protein 53	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533509
11440	Trp53	transformation related protein 53	gene	MP:0010091	decreased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
11440	Trp53	transformation related protein 53	gene	MP:0010094	abnormal chromosome stability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
11440	Trp53	transformation related protein 53	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17097565
11440	Trp53	transformation related protein 53	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0010158	abnormal intestine development		IAGP		N	RGD:5509061	20200820	MGI			PMID:32728212
11440	Trp53	transformation related protein 53	gene	MP:0010173	increased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17653086
11440	Trp53	transformation related protein 53	gene	MP:0010207	abnormal telomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24115439
11440	Trp53	transformation related protein 53	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20190523	MGI			PMID:21282721
11440	Trp53	transformation related protein 53	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20587514
11440	Trp53	transformation related protein 53	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685933
11440	Trp53	transformation related protein 53	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
11440	Trp53	transformation related protein 53	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22172724
11440	Trp53	transformation related protein 53	gene	MP:0010273	increased classified tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
11440	Trp53	transformation related protein 53	gene	MP:0010274	increased organ/body region tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565614
11440	Trp53	transformation related protein 53	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
11440	Trp53	transformation related protein 53	gene	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
11440	Trp53	transformation related protein 53	gene	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319471
11440	Trp53	transformation related protein 53	gene	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451155
11440	Trp53	transformation related protein 53	gene	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948956
11440	Trp53	transformation related protein 53	gene	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23887970
11440	Trp53	transformation related protein 53	gene	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20160922	MGI			PMID:26704996
11440	Trp53	transformation related protein 53	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670909
11440	Trp53	transformation related protein 53	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948956
11440	Trp53	transformation related protein 53	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23887970
11440	Trp53	transformation related protein 53	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851974
11440	Trp53	transformation related protein 53	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
11440	Trp53	transformation related protein 53	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20160505	MGI			PMID:26282165
11440	Trp53	transformation related protein 53	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20160922	MGI			PMID:26704996
11440	Trp53	transformation related protein 53	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20170314	MGI			PMID:27815386
11440	Trp53	transformation related protein 53	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20160512	MGI			PMID:21502497
11440	Trp53	transformation related protein 53	gene	MP:0010280	increased skeletal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0010281	increased nervous system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0010281	increased nervous system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21242963
11440	Trp53	transformation related protein 53	gene	MP:0010281	increased nervous system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23887970
11440	Trp53	transformation related protein 53	gene	MP:0010285	decreased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22172724
11440	Trp53	transformation related protein 53	gene	MP:0010287	increased reproductive system tumor incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0010289	increased urinary system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21151170
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319859
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431698
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694875
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150107
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546942
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17212342
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525270
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626182
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17653086
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20676140
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21324922
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22172724
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24120138
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20160331	MGI			PMID:25330770
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20160428	MGI			PMID:16166291
11440	Trp53	transformation related protein 53	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20190523	MGI			PMID:21282721
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694875
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456863
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17097565
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510390
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626182
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502497
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22172724
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
11440	Trp53	transformation related protein 53	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20180913	MGI			PMID:24162662
11440	Trp53	transformation related protein 53	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546942
11440	Trp53	transformation related protein 53	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029233
11440	Trp53	transformation related protein 53	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
11440	Trp53	transformation related protein 53	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
11440	Trp53	transformation related protein 53	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266220
11440	Trp53	transformation related protein 53	gene	MP:0010307	abnormal tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
11440	Trp53	transformation related protein 53	gene	MP:0010307	abnormal tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
11440	Trp53	transformation related protein 53	gene	MP:0010307	abnormal tumor latency		IAGP		N	RGD:5509061	20210506	MGI			PMID:31794893
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:11280729
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694875
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967151
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16023597
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767157
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:19477430
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22034435
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22172724
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:24115439
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20210506	MGI			PMID:31794893
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20211021	MGI			PMID:28076792
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20230601	MGI			PMID:30093633
11440	Trp53	transformation related protein 53	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20230601	MGI			PMID:36073547
11440	Trp53	transformation related protein 53	gene	MP:0010309	increased mesothelioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0010309	increased mesothelioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0010309	increased mesothelioma incidence		IAGP		N	RGD:5509061	20150507	MGI			PMID:23851502
11440	Trp53	transformation related protein 53	gene	MP:0010310	increased Schwannoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0010310	increased Schwannoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0010312	increased oligodendroglioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12670909
11440	Trp53	transformation related protein 53	gene	MP:0010312	increased oligodendroglioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23887970
11440	Trp53	transformation related protein 53	gene	MP:0010312	increased oligodendroglioma incidence		IAGP		N	RGD:5509061	20160505	MGI			PMID:26282165
11440	Trp53	transformation related protein 53	gene	MP:0010312	increased oligodendroglioma incidence		IAGP		N	RGD:5509061	20160922	MGI			PMID:26704996
11440	Trp53	transformation related protein 53	gene	MP:0010313	increased osteoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0010314	increased neurofibroma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0010315	increased cholangiocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266220
11440	Trp53	transformation related protein 53	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11440	Trp53	transformation related protein 53	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11440	Trp53	transformation related protein 53	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20160811	MGI			PMID:26359368
11440	Trp53	transformation related protein 53	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
11440	Trp53	transformation related protein 53	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22574128
11440	Trp53	transformation related protein 53	gene	MP:0010322	increased cutaneous melanoma incidence		IAGP		N	RGD:5509061	20150827	MGI			PMID:20718941
11440	Trp53	transformation related protein 53	gene	MP:0010334	pleural effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18328429
11440	Trp53	transformation related protein 53	gene	MP:0010337	increased chronic lymphocytic leukemia incidence		IAGP		N	RGD:5509061	20160707	MGI			PMID:19332766
11440	Trp53	transformation related protein 53	gene	MP:0010343	increased lipoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0010343	increased lipoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0010344	increased hibernoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0010344	increased hibernoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23486187
11440	Trp53	transformation related protein 53	gene	MP:0010346	increased thyroid carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19765830
11440	Trp53	transformation related protein 53	gene	MP:0010346	increased thyroid carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11440	Trp53	transformation related protein 53	gene	MP:0010346	increased thyroid carcinoma incidence		IAGP		N	RGD:5509061	20170601	MGI			PMID:22190384
11440	Trp53	transformation related protein 53	gene	MP:0010346	increased thyroid carcinoma incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:24711431
11440	Trp53	transformation related protein 53	gene	MP:0010347	osseous metaplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15221010
11440	Trp53	transformation related protein 53	gene	MP:0010348	increased pancreatic islet cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11440	Trp53	transformation related protein 53	gene	MP:0010348	increased pancreatic islet cell carcinoma incidence		IAGP		N	RGD:5509061	20151008	MGI			PMID:24292676
11440	Trp53	transformation related protein 53	gene	MP:0010349	increased teratocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0010351	increased pituitary melanotroph tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7951317
11440	Trp53	transformation related protein 53	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079851
11440	Trp53	transformation related protein 53	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323676
11440	Trp53	transformation related protein 53	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19779492
11440	Trp53	transformation related protein 53	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17607363
11440	Trp53	transformation related protein 53	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20697345
11440	Trp53	transformation related protein 53	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22358843
11440	Trp53	transformation related protein 53	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20160331	MGI			PMID:25330770
11440	Trp53	transformation related protein 53	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0010537	tumor regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:17251932
11440	Trp53	transformation related protein 53	gene	MP:0010537	tumor regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0010537	tumor regression		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208064
11440	Trp53	transformation related protein 53	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22172724
11440	Trp53	transformation related protein 53	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23845441
11440	Trp53	transformation related protein 53	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20160204	MGI			PMID:14522252
11440	Trp53	transformation related protein 53	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20230601	MGI			PMID:26360410
11440	Trp53	transformation related protein 53	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11440	Trp53	transformation related protein 53	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891301
11440	Trp53	transformation related protein 53	gene	MP:0010715	retina coloboma		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0010727	increased glioblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973261
11440	Trp53	transformation related protein 53	gene	MP:0010727	increased glioblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948956
11440	Trp53	transformation related protein 53	gene	MP:0010727	increased glioblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625383
11440	Trp53	transformation related protein 53	gene	MP:0010727	increased glioblastoma incidence		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
11440	Trp53	transformation related protein 53	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
11440	Trp53	transformation related protein 53	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
11440	Trp53	transformation related protein 53	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20180215	MGI			PMID:28294115
11440	Trp53	transformation related protein 53	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20180503	MGI			PMID:29358667
11440	Trp53	transformation related protein 53	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23285300
11440	Trp53	transformation related protein 53	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20181129	MGI			PMID:30042151
11440	Trp53	transformation related protein 53	gene	MP:0010918	abnormal pulmonary neuroendocrine body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047698
11440	Trp53	transformation related protein 53	gene	MP:0010952	abnormal fatty acid beta-oxidation		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
11440	Trp53	transformation related protein 53	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
11440	Trp53	transformation related protein 53	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:31197172
11440	Trp53	transformation related protein 53	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
11440	Trp53	transformation related protein 53	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
11440	Trp53	transformation related protein 53	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332968
11440	Trp53	transformation related protein 53	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
11440	Trp53	transformation related protein 53	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
11440	Trp53	transformation related protein 53	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17129780
11440	Trp53	transformation related protein 53	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
11440	Trp53	transformation related protein 53	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
11440	Trp53	transformation related protein 53	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
11440	Trp53	transformation related protein 53	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729946
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216268
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20671749
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:30858352
11440	Trp53	transformation related protein 53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10191063
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172844
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337066
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
11440	Trp53	transformation related protein 53	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20190418	MGI			PMID:27528230
11440	Trp53	transformation related protein 53	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859164
11440	Trp53	transformation related protein 53	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906694
11440	Trp53	transformation related protein 53	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29262616
11440	Trp53	transformation related protein 53	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980714
11440	Trp53	transformation related protein 53	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
11440	Trp53	transformation related protein 53	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884603
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832489
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654339
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790550
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17000755
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170753
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24209622
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207798
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872327
11440	Trp53	transformation related protein 53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
11440	Trp53	transformation related protein 53	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16007073
11440	Trp53	transformation related protein 53	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20160310	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
11440	Trp53	transformation related protein 53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
11440	Trp53	transformation related protein 53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340312
11440	Trp53	transformation related protein 53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
11440	Trp53	transformation related protein 53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
11440	Trp53	transformation related protein 53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
11440	Trp53	transformation related protein 53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
11440	Trp53	transformation related protein 53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:34601382
11440	Trp53	transformation related protein 53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20240808	MGI			PMID:37306301
11440	Trp53	transformation related protein 53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
11440	Trp53	transformation related protein 53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
11440	Trp53	transformation related protein 53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15081359
11440	Trp53	transformation related protein 53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181534
11440	Trp53	transformation related protein 53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
11440	Trp53	transformation related protein 53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
11440	Trp53	transformation related protein 53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
11440	Trp53	transformation related protein 53	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
11440	Trp53	transformation related protein 53	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
11440	Trp53	transformation related protein 53	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470788
11440	Trp53	transformation related protein 53	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
11440	Trp53	transformation related protein 53	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21127973
11440	Trp53	transformation related protein 53	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:34601382
11440	Trp53	transformation related protein 53	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21127973
11440	Trp53	transformation related protein 53	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17289567
11440	Trp53	transformation related protein 53	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
11440	Trp53	transformation related protein 53	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
11440	Trp53	transformation related protein 53	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20181227	MGI			PMID:18641651
11440	Trp53	transformation related protein 53	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20181227	MGI			PMID:18641651
11440	Trp53	transformation related protein 53	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502497
11440	Trp53	transformation related protein 53	gene	MP:0011638	abnormal mitochondrial chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199867
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21127973
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150212	MGI			PMID:10508513
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:10911993
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:10973245
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:11431698
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:12101245
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:15607980
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:16007073
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:16023597
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20151112	MGI			PMID:22606359
11440	Trp53	transformation related protein 53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20190711	MGI			PMID:29635765
11440	Trp53	transformation related protein 53	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
11440	Trp53	transformation related protein 53	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23798389
11440	Trp53	transformation related protein 53	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
11440	Trp53	transformation related protein 53	gene	MP:0011804	increased cell migration		IAGP		N	RGD:5509061	20161013	MGI			PMID:26659571
11440	Trp53	transformation related protein 53	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0012043	increased myoepithelioma incidence		IAGP		N	RGD:5509061	20160331	MGI			PMID:25330770
11440	Trp53	transformation related protein 53	gene	MP:0012400	nail dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
11440	Trp53	transformation related protein 53	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20161222	MGI			PMID:27354067
11440	Trp53	transformation related protein 53	gene	MP:0012415	decreased sarcoma incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
11440	Trp53	transformation related protein 53	gene	MP:0012415	decreased sarcoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
11440	Trp53	transformation related protein 53	gene	MP:0012416	decreased gland tumor incidence		IAGP		N	RGD:5509061	20231102	MGI			PMID:36241718
11440	Trp53	transformation related protein 53	gene	MP:0012416	decreased gland tumor incidence		IAGP		N	RGD:5509061	20250605	MGI			PMID:31048544
11440	Trp53	transformation related protein 53	gene	MP:0012424	decreased alimentary system tumor incidence		IAGP		N	RGD:5509061	20200820	MGI			PMID:32728212
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346812
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591653
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11169961
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696456
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956084
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967151
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12414647
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914701
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14702042
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150107
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1552940
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821748
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227443
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486075
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510390
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906694
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17984302
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767771
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19881536
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473325
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21324922
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23665223
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029233
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24115439
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:9861017
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25119042
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:25144937
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160428	MGI			PMID:16166291
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23538418
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20190711	MGI			PMID:29635765
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20260312	MGI			PMID:34406363
11440	Trp53	transformation related protein 53	gene	MP:0012690	abnormal stride length		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
11440	Trp53	transformation related protein 53	gene	MP:0013177	abnormal tail tip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013501
11440	Trp53	transformation related protein 53	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894267
11440	Trp53	transformation related protein 53	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20150319	MGI			PMID:22617326
11440	Trp53	transformation related protein 53	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20150507	MGI			PMID:23851502
11440	Trp53	transformation related protein 53	gene	MP:0013221	pancreatic acinar-to-ductal metaplasia		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
11440	Trp53	transformation related protein 53	gene	MP:0013236	ovary degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23741457
11440	Trp53	transformation related protein 53	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790550
11440	Trp53	transformation related protein 53	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
11440	Trp53	transformation related protein 53	gene	MP:0013374	increased sebaceous gland tumor incidence		IAGP		N	RGD:5509061	20180913	MGI			PMID:24162662
11440	Trp53	transformation related protein 53	gene	MP:0013483	abnormal jejunum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200820	MGI			PMID:32728212
11440	Trp53	transformation related protein 53	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16616333
11440	Trp53	transformation related protein 53	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17170753
11440	Trp53	transformation related protein 53	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:19620979
11440	Trp53	transformation related protein 53	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:11431698
11440	Trp53	transformation related protein 53	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
11440	Trp53	transformation related protein 53	gene	MP:0013505	decreased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17325035
11440	Trp53	transformation related protein 53	gene	MP:0013539	increased ovary adenoma incidence		IAGP		N	RGD:5509061	20161222	MGI			PMID:27354067
11440	Trp53	transformation related protein 53	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
11440	Trp53	transformation related protein 53	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:19966810
11440	Trp53	transformation related protein 53	gene	MP:0013705	decreased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:19966810
11440	Trp53	transformation related protein 53	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20190523	MGI			PMID:21282721
11440	Trp53	transformation related protein 53	gene	MP:0013751	increased cystadenoma incidence		IAGP		N	RGD:5509061	20170615	MGI			PMID:26411367
11440	Trp53	transformation related protein 53	gene	MP:0013958	decreased small intestine length		IAGP		N	RGD:5509061	20220721	MGI			PMID:34376666
11440	Trp53	transformation related protein 53	gene	MP:0014040	increased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20181129	MGI			PMID:30042151
11440	Trp53	transformation related protein 53	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:12642502
11440	Trp53	transformation related protein 53	gene	MP:0014127	increased thymoma incidence		IAGP		N	RGD:5509061	20160317	MGI			PMID:21552324
11440	Trp53	transformation related protein 53	gene	MP:0014127	increased thymoma incidence		IAGP		N	RGD:5509061	20160317	MGI			PMID:9584189
11440	Trp53	transformation related protein 53	gene	MP:0014127	increased thymoma incidence		IAGP		N	RGD:5509061	20180906	MGI			PMID:25565005
11440	Trp53	transformation related protein 53	gene	MP:0014234	decreased enterocyte apoptosis		IAGP		N	RGD:5509061	20230323	MGI			PMID:10097137
11440	Trp53	transformation related protein 53	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21674502
11440	Trp53	transformation related protein 53	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:25985210
11440	Trp53	transformation related protein 53	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:29743593
11440	Trp53	transformation related protein 53	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:33594717
11440	Trp53	transformation related protein 53	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:35700263
11440	Trp53	transformation related protein 53	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11440	Trp53	transformation related protein 53	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230615	MGI			PMID:34803166
11440	Trp53	transformation related protein 53	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:10077642
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:10346812
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:10760284
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:10973261
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:12839925
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:14647411
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:14702042
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:15231717
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:15652750
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:17417627
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:17533180
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:17906694
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:18202109
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:19767771
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21277975
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:22341455
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:22411819
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:22682249
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:22896338
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23285300
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:24029233
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:24120138
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:24292676
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:24711431
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:29743593
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:31483066
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:35700263
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:7922305
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230615	MGI			PMID:34803166
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
11440	Trp53	transformation related protein 53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20260312	MGI			PMID:34406363
11440	Trp53	transformation related protein 53	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:27354067
11440	Trp53	transformation related protein 53	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:12642502
11440	Trp53	transformation related protein 53	gene	MP:0014754	abnormal tumor progression		IAGP		N	RGD:5509061	20250904	MGI			PMID:33594717
11440	Trp53	transformation related protein 53	gene	MP:0014754	abnormal tumor progression		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
11440	Trp53	transformation related protein 53	gene	MP:0014755	increased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:21799785
11440	Trp53	transformation related protein 53	gene	MP:0014755	increased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:26360410
11440	Trp53	transformation related protein 53	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:33594717
11440	Trp53	transformation related protein 53	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
11440	Trp53	transformation related protein 53	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:33594717
11440	Trp53	transformation related protein 53	gene	MP:0014758	decreased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:21285512
11440	Trp53	transformation related protein 53	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
11440	Trp53	transformation related protein 53	gene	MP:0020386	adipose tissue inflammation		IAGP		N	RGD:5509061	20161117	MGI			PMID:21411755
11440	Trp53	transformation related protein 53	gene	MP:0020410	increased liposarcoma incidence		IAGP		N	RGD:5509061	20180111	MGI			PMID:22293175
11440	Trp53	transformation related protein 53	gene	MP:0020427	increased hepatocyte karyomegaly		IAGP		N	RGD:5509061	20210422	MGI			PMID:32381628
11440	Trp53	transformation related protein 53	gene	MP:0021056	abnormal tumor vascular morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:35700263
11440	Trp53	transformation related protein 53	gene	MP:0021085	increased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:15607981
11440	Trp53	transformation related protein 53	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:10393064
11440	Trp53	transformation related protein 53	gene	MP:0021184	decreased bone mineral density of humerus		IAGP		N	RGD:5509061	20220915	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:15231717
11440	Trp53	transformation related protein 53	gene	MP:0030073	square face		IAGP		N	RGD:5509061	20170921	MGI			PMID:25119037
11440	Trp53	transformation related protein 53	gene	MP:0030737	decreased glutamic acid level		IAGP		N	RGD:5509061	20191205	MGI			PMID:31685994
11440	Trp53	transformation related protein 53	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:22341455
11440	Trp53	transformation related protein 53	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:23770245
11440	Trp53	transformation related protein 53	gene	MP:0030928	increased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:22341455
11440	Trp53	transformation related protein 53	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
11440	Trp53	transformation related protein 53	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:17607363
11440	Trp53	transformation related protein 53	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:24706806
11440	Trp53	transformation related protein 53	gene	MP:0031058	hepatosplenomegaly		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
11440	Trp53	transformation related protein 53	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:11780111
11440	Trp53	transformation related protein 53	gene	MP:0031278	decreased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:29743593
11440	Trp53	transformation related protein 53	gene	MP:0031278	decreased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:35700263
11440	Trp53	transformation related protein 53	gene	MP:0031278	decreased osteosarcoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:28655788
11440	Trp53	transformation related protein 53	gene	MP:0031278	decreased osteosarcoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:34803166
11440	Trp53	transformation related protein 53	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:22579044
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20230601	MGI			PMID:35243414
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9400381
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440710
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20230601	MGI			PMID:35243414
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20230601	MGI			PMID:35243414
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20230601	MGI			PMID:35243414
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20230601	MGI			PMID:35243414
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9440710
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20230601	MGI			PMID:35243414
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9400381
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20230601	MGI			PMID:35243414
11445	Tpm1	tropomyosin 1, alpha	gene	MP:0012700	abnormal endocardial heart tube morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:35243414
11452	Trh	thyrotropin releasing hormone	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20181227	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380725
11452	Trh	thyrotropin releasing hormone	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380725
11452	Trh	thyrotropin releasing hormone	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20181227	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380725
11452	Trh	thyrotropin releasing hormone	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20181227	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20181227	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380725
11452	Trh	thyrotropin releasing hormone	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10628753
11452	Trh	thyrotropin releasing hormone	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380725
11452	Trh	thyrotropin releasing hormone	gene	MP:0005119	decreased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10628753
11452	Trh	thyrotropin releasing hormone	gene	MP:0005135	increased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9380725
11452	Trh	thyrotropin releasing hormone	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20200402	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220519	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10628753
11452	Trh	thyrotropin releasing hormone	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20250508	MGI			
11452	Trh	thyrotropin releasing hormone	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17666589
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17666589
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0003351	decreased circulating levels of thyroid hormone		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988432
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0005471	decreased thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988432
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0005473	decreased triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988432
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17666589
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17666589
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0011611	abnormal circulating ghrelin level		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0011612	increased circulating ghrelin level		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11453	Trhr	thyrotropin releasing hormone receptor	gene	MP:0011613	decreased circulating ghrelin level		IAGP		N	RGD:5509061	20150611	MGI			PMID:25490146
11457	Tsc2	TSC complex subunit 2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0000275	heart hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491404
11457	Tsc2	TSC complex subunit 2	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
11457	Tsc2	TSC complex subunit 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419848
11457	Tsc2	TSC complex subunit 2	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419848
11457	Tsc2	TSC complex subunit 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
11457	Tsc2	TSC complex subunit 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
11457	Tsc2	TSC complex subunit 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
11457	Tsc2	TSC complex subunit 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
11457	Tsc2	TSC complex subunit 2	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11457	Tsc2	TSC complex subunit 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20150702	MGI			PMID:23250422
11457	Tsc2	TSC complex subunit 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20170223	MGI			PMID:25155956
11457	Tsc2	TSC complex subunit 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419848
11457	Tsc2	TSC complex subunit 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419848
11457	Tsc2	TSC complex subunit 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419848
11457	Tsc2	TSC complex subunit 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18568033
11457	Tsc2	TSC complex subunit 2	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18568033
11457	Tsc2	TSC complex subunit 2	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11457	Tsc2	TSC complex subunit 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
11457	Tsc2	TSC complex subunit 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491404
11457	Tsc2	TSC complex subunit 2	gene	MP:0002045	increased renal cystadenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491404
11457	Tsc2	TSC complex subunit 2	gene	MP:0002045	increased renal cystadenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491404
11457	Tsc2	TSC complex subunit 2	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491404
11457	Tsc2	TSC complex subunit 2	gene	MP:0002049	increased extremity angiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491404
11457	Tsc2	TSC complex subunit 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062901
11457	Tsc2	TSC complex subunit 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419848
11457	Tsc2	TSC complex subunit 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062901
11457	Tsc2	TSC complex subunit 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
11457	Tsc2	TSC complex subunit 2	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062901
11457	Tsc2	TSC complex subunit 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
11457	Tsc2	TSC complex subunit 2	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20150702	MGI			PMID:23250422
11457	Tsc2	TSC complex subunit 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
11457	Tsc2	TSC complex subunit 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18568033
11457	Tsc2	TSC complex subunit 2	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21737790
11457	Tsc2	TSC complex subunit 2	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21737790
11457	Tsc2	TSC complex subunit 2	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20150702	MGI			PMID:23250422
11457	Tsc2	TSC complex subunit 2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062901
11457	Tsc2	TSC complex subunit 2	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20170223	MGI			PMID:25155956
11457	Tsc2	TSC complex subunit 2	gene	MP:0003570	increased uterus leiomyoma incidence		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11457	Tsc2	TSC complex subunit 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
11457	Tsc2	TSC complex subunit 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
11457	Tsc2	TSC complex subunit 2	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11457	Tsc2	TSC complex subunit 2	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11457	Tsc2	TSC complex subunit 2	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062901
11457	Tsc2	TSC complex subunit 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11457	Tsc2	TSC complex subunit 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25880340
11457	Tsc2	TSC complex subunit 2	gene	MP:0008256	abnormal myometrium morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11457	Tsc2	TSC complex subunit 2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20170223	MGI			PMID:25155956
11457	Tsc2	TSC complex subunit 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062901
11457	Tsc2	TSC complex subunit 2	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11457	Tsc2	TSC complex subunit 2	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
11457	Tsc2	TSC complex subunit 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25880340
11457	Tsc2	TSC complex subunit 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:25155956
11457	Tsc2	TSC complex subunit 2	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062901
11457	Tsc2	TSC complex subunit 2	gene	MP:0010294	increased kidney tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316403
11457	Tsc2	TSC complex subunit 2	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0010384	increased renal carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0010384	increased renal carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491404
11457	Tsc2	TSC complex subunit 2	gene	MP:0010656	thick myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
11457	Tsc2	TSC complex subunit 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419848
11457	Tsc2	TSC complex subunit 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491404
11457	Tsc2	TSC complex subunit 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357198
11457	Tsc2	TSC complex subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
11457	Tsc2	TSC complex subunit 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10096549
11457	Tsc2	TSC complex subunit 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17245776
11457	Tsc2	TSC complex subunit 2	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
11457	Tsc2	TSC complex subunit 2	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20150709	MGI			PMID:23820898
11457	Tsc2	TSC complex subunit 2	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20170223	MGI			PMID:25155956
11457	Tsc2	TSC complex subunit 2	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20190711	MGI			PMID:25155956
11457	Tsc2	TSC complex subunit 2	gene	MP:0031407	increased Sertoli cell proliferation		IAGP		N	RGD:5509061	20220630	MGI			PMID:22791749
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10575115
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530227
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530227
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530227
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7209519
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530227
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001396	unidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530227
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530227
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7209519
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001922	reduced male fertility		IEA		N	RGD:5509061	20141003	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001923	reduced female fertility		IEA		N	RGD:5509061	20141003	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7209519
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7209519
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16780814
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20141003	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0002876	abnormal thyroid gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20160714	MGI			PMID:21220306
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10575115
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003194	abnormal frequency of paradoxical sleep		IAGP		N	RGD:5509061	20141003	MGI			PMID:11690529
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003351	decreased circulating levels of thyroid hormone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003356	impaired luteinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11690529
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003501	iodide oxidation defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0003718	maternal effect		IEA		N	RGD:5509061	20141003	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11690529
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0004022	abnormal cone electrophysiology		IEA		N	RGD:5509061	20141003	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10575115
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10575115
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10575115
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7209519
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20160714	MGI			PMID:21220306
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10570273
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7209519
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005135	increased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7209519
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11690529
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005468	abnormal thyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005471	decreased thyroxine level		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7209519
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10570273
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0008337	increased thyrotroph cell number		IEA		N	RGD:5509061	20141127	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0008974	proportional dwarf		IEA		N	RGD:5509061	20141003	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11690529
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20160714	MGI			PMID:21220306
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20171228	MGI			PMID:18559984
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432094
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0011084	lethality at weaning, incomplete penetrance		IEA		N	RGD:5509061	20141003	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20141003	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530227
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10575115
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16780814
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0012144	decreased b-wave amplitude		IEA		N	RGD:5509061	20141003	MGI			
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20240405	MGI			PMID:10575115
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20240405	MGI			PMID:10575115
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20151112	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0021194	decreased bone mineral density of caudal vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:17932107
11458	Tshr	thyroid stimulating hormone receptor	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:11690529
11459	Tspy-ps	testis specific protein-Y encoded, pseudogene	gene	MP:0003397	increased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15851664
11459	Tspy-ps	testis specific protein-Y encoded, pseudogene	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15851664
11460	Tst	thiosulfate sulfurtransferase, mitochondrial	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
11460	Tst	thiosulfate sulfurtransferase, mitochondrial	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20170105	MGI			
11460	Tst	thiosulfate sulfurtransferase, mitochondrial	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20170105	MGI			
11460	Tst	thiosulfate sulfurtransferase, mitochondrial	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
11460	Tst	thiosulfate sulfurtransferase, mitochondrial	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20160811	MGI			
11460	Tst	thiosulfate sulfurtransferase, mitochondrial	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20160811	MGI			
11460	Tst	thiosulfate sulfurtransferase, mitochondrial	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
11466	Tyr	tyrosinase	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:521742
11466	Tyr	tyrosinase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:1033984
11466	Tyr	tyrosinase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215665
11466	Tyr	tyrosinase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572362
11466	Tyr	tyrosinase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:21968110
11466	Tyr	tyrosinase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:4296364
11466	Tyr	tyrosinase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:4823665
11466	Tyr	tyrosinase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:6793688
11466	Tyr	tyrosinase	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1822431
11466	Tyr	tyrosinase	gene	MP:0000373	belly spot		IEA		N	RGD:5509061	20120202	MGI			
11466	Tyr	tyrosinase	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20141003	MGI			PMID:6793688
11466	Tyr	tyrosinase	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023352
11466	Tyr	tyrosinase	gene	MP:0000411	shiny fur		IEA		N	RGD:5509061	20111116	MGI			
11466	Tyr	tyrosinase	gene	MP:0000421	mottled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023352
11466	Tyr	tyrosinase	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925014
11466	Tyr	tyrosinase	gene	MP:0001189	absent skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10325425
11466	Tyr	tyrosinase	gene	MP:0001189	absent skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943097
11466	Tyr	tyrosinase	gene	MP:0001189	absent skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6793688
11466	Tyr	tyrosinase	gene	MP:0001189	absent skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8921397
11466	Tyr	tyrosinase	gene	MP:0001224	abnormal keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
11466	Tyr	tyrosinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20181206	MGI			PMID:18469339
11466	Tyr	tyrosinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
11466	Tyr	tyrosinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20111116	MGI			
11466	Tyr	tyrosinase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20111116	MGI			
11466	Tyr	tyrosinase	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572362
11466	Tyr	tyrosinase	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040030
11466	Tyr	tyrosinase	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161869
11466	Tyr	tyrosinase	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161869
11466	Tyr	tyrosinase	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20181206	MGI			PMID:18469339
11466	Tyr	tyrosinase	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20181206	MGI			PMID:18469339
11466	Tyr	tyrosinase	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20180614	MGI			
11466	Tyr	tyrosinase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20181206	MGI			PMID:17024248
11466	Tyr	tyrosinase	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20181206	MGI			PMID:17024248
11466	Tyr	tyrosinase	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20181206	MGI			PMID:18469339
11466	Tyr	tyrosinase	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20181206	MGI			PMID:17024248
11466	Tyr	tyrosinase	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20111116	MGI			
11466	Tyr	tyrosinase	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
11466	Tyr	tyrosinase	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:24124512
11466	Tyr	tyrosinase	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:24124512
11466	Tyr	tyrosinase	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20120202	MGI			
11466	Tyr	tyrosinase	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20180614	MGI			
11466	Tyr	tyrosinase	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1033984
11466	Tyr	tyrosinase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12955145
11466	Tyr	tyrosinase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1618394
11466	Tyr	tyrosinase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1822431
11466	Tyr	tyrosinase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:4296364
11466	Tyr	tyrosinase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:4823665
11466	Tyr	tyrosinase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8200511
11466	Tyr	tyrosinase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023352
11466	Tyr	tyrosinase	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:2304907
11466	Tyr	tyrosinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625383
11466	Tyr	tyrosinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:574104
11466	Tyr	tyrosinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7117820
11466	Tyr	tyrosinase	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:11925014
11466	Tyr	tyrosinase	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023352
11466	Tyr	tyrosinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24823394
11466	Tyr	tyrosinase	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20181206	MGI			PMID:18469339
11466	Tyr	tyrosinase	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21494554
11466	Tyr	tyrosinase	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20181206	MGI			PMID:18469339
11466	Tyr	tyrosinase	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20181206	MGI			PMID:17024248
11466	Tyr	tyrosinase	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:521742
11466	Tyr	tyrosinase	gene	MP:0003136	yellow coat color		IEA		N	RGD:5509061	20111116	MGI			
11466	Tyr	tyrosinase	gene	MP:0003234	enhanced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
11466	Tyr	tyrosinase	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20141003	MGI			PMID:521742
11466	Tyr	tyrosinase	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20120202	MGI			
11466	Tyr	tyrosinase	gene	MP:0003642	absent seminal vesicle		IEA		N	RGD:5509061	20120202	MGI			
11466	Tyr	tyrosinase	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4141683
11466	Tyr	tyrosinase	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625383
11466	Tyr	tyrosinase	gene	MP:0003962	abnormal adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11466	Tyr	tyrosinase	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11466	Tyr	tyrosinase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
11466	Tyr	tyrosinase	gene	MP:0003996	clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:4823665
11466	Tyr	tyrosinase	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:4141683
11466	Tyr	tyrosinase	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:4823665
11466	Tyr	tyrosinase	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
11466	Tyr	tyrosinase	gene	MP:0004222	iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
11466	Tyr	tyrosinase	gene	MP:0004226	absent Schlemm's canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
11466	Tyr	tyrosinase	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
11466	Tyr	tyrosinase	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943097
11466	Tyr	tyrosinase	gene	MP:0004382	abnormal hair follicle melanogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6793688
11466	Tyr	tyrosinase	gene	MP:0004382	abnormal hair follicle melanogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7688401
11466	Tyr	tyrosinase	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
11466	Tyr	tyrosinase	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
11466	Tyr	tyrosinase	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
11466	Tyr	tyrosinase	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21968110
11466	Tyr	tyrosinase	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11466	Tyr	tyrosinase	gene	MP:0005077	abnormal melanogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11466	Tyr	tyrosinase	gene	MP:0005102	abnormal iris pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21968110
11466	Tyr	tyrosinase	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10325425
11466	Tyr	tyrosinase	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1352884
11466	Tyr	tyrosinase	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1618394
11466	Tyr	tyrosinase	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21968110
11466	Tyr	tyrosinase	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24879364
11466	Tyr	tyrosinase	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:4296364
11466	Tyr	tyrosinase	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8200511
11466	Tyr	tyrosinase	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141016	MGI			PMID:24599260
11466	Tyr	tyrosinase	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10325425
11466	Tyr	tyrosinase	gene	MP:0005174	abnormal tail pigmentation		IEA		N	RGD:5509061	20170209	MGI			
11466	Tyr	tyrosinase	gene	MP:0005198	abnormal aqueous drainage system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
11466	Tyr	tyrosinase	gene	MP:0005203	abnormal trabecular meshwork morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12624268
11466	Tyr	tyrosinase	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040030
11466	Tyr	tyrosinase	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3596986
11466	Tyr	tyrosinase	gene	MP:0005257	abnormal intraocular pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532192
11466	Tyr	tyrosinase	gene	MP:0005366	variegated coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572362
11466	Tyr	tyrosinase	gene	MP:0005408	hypopigmentation		IEA		N	RGD:5509061	20111116	MGI			
11466	Tyr	tyrosinase	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11466	Tyr	tyrosinase	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
11466	Tyr	tyrosinase	gene	MP:0006159	ocular albinism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18715234
11466	Tyr	tyrosinase	gene	MP:0006159	ocular albinism		IAGP		N	RGD:5509061	20141003	MGI			PMID:21968110
11466	Tyr	tyrosinase	gene	MP:0006159	ocular albinism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023352
11466	Tyr	tyrosinase	gene	MP:0006370	abnormal hair follicle pheomelanosome pheomelanin content		IEA		N	RGD:5509061	20141003	MGI			
11466	Tyr	tyrosinase	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215665
11466	Tyr	tyrosinase	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1618394
11466	Tyr	tyrosinase	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24879364
11466	Tyr	tyrosinase	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8200511
11466	Tyr	tyrosinase	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023352
11466	Tyr	tyrosinase	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20141016	MGI			PMID:24599260
11466	Tyr	tyrosinase	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21494554
11466	Tyr	tyrosinase	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21494554
11466	Tyr	tyrosinase	gene	MP:0008770	decreased survivor rate		IEA		N	RGD:5509061	20111116	MGI			
11466	Tyr	tyrosinase	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20150514	MGI			PMID:1063212
11466	Tyr	tyrosinase	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150514	MGI			PMID:1063212
11466	Tyr	tyrosinase	gene	MP:0009287	decreased abdominal fat pad weight		IAGP		N	RGD:5509061	20181206	MGI			PMID:18469339
11466	Tyr	tyrosinase	gene	MP:0010192	abnormal retina melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11466	Tyr	tyrosinase	gene	MP:0010193	abnormal choroid melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11466	Tyr	tyrosinase	gene	MP:0010231	transverse fur striping		IAGP		N	RGD:5509061	20141003	MGI			PMID:1822431
11466	Tyr	tyrosinase	gene	MP:0010727	increased glioblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625383
11466	Tyr	tyrosinase	gene	MP:0010769	abnormal survival		IEA		N	RGD:5509061	20120202	MGI			
11466	Tyr	tyrosinase	gene	MP:0011002	enhanced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:574104
11466	Tyr	tyrosinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7117820
11466	Tyr	tyrosinase	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215665
11466	Tyr	tyrosinase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10212311
11466	Tyr	tyrosinase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
11466	Tyr	tyrosinase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2304907
11466	Tyr	tyrosinase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8200511
11466	Tyr	tyrosinase	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:574104
11466	Tyr	tyrosinase	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7117820
11466	Tyr	tyrosinase	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:521742
11466	Tyr	tyrosinase	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:574104
11466	Tyr	tyrosinase	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7117820
11466	Tyr	tyrosinase	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:24124512
11466	Tyr	tyrosinase	gene	MP:0011233	abnormal vitamin A metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606814
11466	Tyr	tyrosinase	gene	MP:0011277	decreased tail pigmentation		IEA		N	RGD:5509061	20170126	MGI			
11466	Tyr	tyrosinase	gene	MP:0011279	decreased ear pigmentation		IEA		N	RGD:5509061	20170126	MGI			
11466	Tyr	tyrosinase	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20150430	MGI			PMID:12624268
11466	Tyr	tyrosinase	gene	MP:0011551	variegated eye pigmentation pattern		IEA		N	RGD:5509061	20170126	MGI			
11466	Tyr	tyrosinase	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161869
11466	Tyr	tyrosinase	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161869
11466	Tyr	tyrosinase	gene	MP:0014375	increased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:20130004
11466	Tyr	tyrosinase	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20181206	MGI			PMID:18469339
11466	Tyr	tyrosinase	gene	MP:0031434	increased miscarriage rate		IEA		N	RGD:5509061	20220915	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20190425	MGI			PMID:28093506
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20190425	MGI			PMID:28093506
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28093506
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18393392
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18393392
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20190425	MGI			PMID:28093506
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190425	MGI			PMID:28093506
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002425	abnormal susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0004083	polysyndactyly		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28093506
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18393392
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20230119	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20190425	MGI			PMID:28093506
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20201119	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20190425	MGI			PMID:28093506
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11452127
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0009012	short diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0009014	prolonged proestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0009322	increased splenocyte apoptosis		IAGP		N	RGD:5509061	20201119	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0009357	abnormal seizure response to inducing agent		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0009396	small endometrial glands		IAGP		N	RGD:5509061	20150326	MGI			PMID:18393392
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0009853	decreased Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18159085
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20250508	MGI			
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20190425	MGI			PMID:28093506
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20201119	MGI			PMID:10227296
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0014551	impaired neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:18787040
11467	Tyro3	TYRO3 protein tyrosine kinase 3	gene	MP:0031168	abnormal brain thrombosis		IAGP		N	RGD:5509061	20201119	MGI			PMID:11452127
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000018	small ears		IEA		N	RGD:5509061	20141003	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248019
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248019
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12644183
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:1303241
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:15415586
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:5726144
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000372	irregular coat pigmentation		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000423	delayed hair regrowth		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000427	abnormal hair cycle		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20171109	MGI			PMID:20460369
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000440	domed cranium		IEA		N	RGD:5509061	20141003	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:20460369
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10192392
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16827931
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247639
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20171109	MGI			PMID:6831040
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001922	reduced male fertility		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001923	reduced female fertility		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248019
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15415586
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247639
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2245917
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5726144
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248019
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248019
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354038
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002630	abnormal endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248019
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247639
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5726144
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0002938	white spotting		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0003136	yellow coat color		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0003878	abnormal ear physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248019
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20171109	MGI			PMID:6466874
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:6466874
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0004367	abnormal strial intermediate cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248019
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:8248019
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005071	enlarged hair follicle melanin granules		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005072	abnormal hair follicle melanin granule morphology		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005102	abnormal iris pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16827931
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005102	abnormal iris pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18715234
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005114	premature hair loss		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005172	decreased eye pigmentation		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005199	abnormal iris pigment epithelium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10192392
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005208	abnormal iris stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10192392
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005257	abnormal intraocular pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16827931
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0005607	decreased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0006228	iris atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16827931
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10192392
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0008238	abnormal dorsoventral coat patterning		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0008731	abnormal hair shaft melanin granule morphology		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0008732	reduced hair shaft melanin granule number		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0008733	abnormal hair shaft melanin granule distribution		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20171109	MGI			PMID:16219534
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0010192	abnormal retina melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0010193	abnormal choroid melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0011089	perinatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0011277	decreased tail pigmentation		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0011279	decreased ear pigmentation		IEA		N	RGD:5509061	20111116	MGI			
11468	Tyrp1	tyrosinase-related protein 1	gene	MP:0012010	parturition failure		IAGP		N	RGD:5509061	20191219	MGI			PMID:1756209
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20201022	MGI			
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16326389
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16326389
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16326389
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16326389
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11469	Ube2i	ubiquitin-conjugating enzyme E2I	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748195
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18713955
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748196
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748195
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18713955
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748195
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748195
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11707458
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18713955
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748196
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274222
11474	Ucp3	uncoupling protein 3 (mitochondrial, proton carrier)	gene	MP:0031414	decreased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:16455084
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9162006
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:9162006
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9162006
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548776
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411819
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11045570
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9162006
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543320
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497281
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002277	abnormal respiratory mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8897914
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20190627	MGI			PMID:10470078
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9162006
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0003115	abnormal respiratory system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0004390	abnormal bronchoalveolar duct junction morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411819
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9162006
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20190627	MGI			PMID:10470078
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20190627	MGI			PMID:10470078
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0005488	bronchial epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548776
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281487
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:8897914
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0009148	pancreas necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9162006
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411819
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20190627	MGI			PMID:10470078
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0010910	bronchiolar epithelial hyperplasia		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0011566	abnormal complement protein level		IAGP		N	RGD:5509061	20190627	MGI			PMID:10470078
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:22411819
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28513596
11475	Scgb1a1	secretoglobin, family 1A, member 1	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:28513596
11477	Umod	uromodulin	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522986
11477	Umod	uromodulin	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665435
11477	Umod	uromodulin	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0002829	abnormal juxtaglomerular apparatus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522986
11477	Umod	uromodulin	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11477	Umod	uromodulin	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0002963	decreased urine protein level		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0002987	abnormal urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522986
11477	Umod	uromodulin	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11477	Umod	uromodulin	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11477	Umod	uromodulin	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11477	Umod	uromodulin	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0005360	urolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0005527	increased renal glomerular filtration rate		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522986
11477	Umod	uromodulin	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0005557	increased creatinine clearance		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522986
11477	Umod	uromodulin	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0006272	abnormal urine organic anion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11477	Umod	uromodulin	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11477	Umod	uromodulin	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0009644	uremia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0009645	crystalluria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11477	Umod	uromodulin	gene	MP:0009810	increased urine uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11477	Umod	uromodulin	gene	MP:0009810	increased urine uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011331	abnormal papillary duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0011344	abnormal loop of Henle ascending limb thick segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15522986
11477	Umod	uromodulin	gene	MP:0011344	abnormal loop of Henle ascending limb thick segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0011424	decreased urine uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011424	decreased urine uric acid level		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0011431	increased urine flow rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011432	decreased urine flow rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0011435	increased urine magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0011435	increased urine magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898038
11477	Umod	uromodulin	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0011465	abnormal urine urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011470	increased urine creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0011471	decreased urine creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20180628	MGI			PMID:28325753
11477	Umod	uromodulin	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011735	increased urine ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20591941
11477	Umod	uromodulin	gene	MP:0011891	decreased circulating ferritin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011894	decreased circulating transferrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748428
11477	Umod	uromodulin	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17264314
11477	Umod	uromodulin	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0012046	decreased susceptibility to hypertension		IAGP		N	RGD:5509061	20190321	MGI			PMID:24324041
11477	Umod	uromodulin	gene	MP:0013305	isosthenuria		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0014810	increased circulating urea level		IAGP		N	RGD:5509061	20251204	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20160421	MGI			PMID:19692485
11477	Umod	uromodulin	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20180712	MGI			PMID:28990932
11477	Umod	uromodulin	gene	MP:0030779	decreased urine citrate level		IAGP		N	RGD:5509061	20181004	MGI			PMID:20591941
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769895
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769895
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17379066
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769895
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769895
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257141
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9322371
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769895
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17379066
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769895
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17379066
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0003057	abnormal epicardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20160128	MGI			PMID:26034041
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0004557	dilated allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257141
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257141
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257141
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257141
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257141
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257141
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257141
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11257140
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769895
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0010555	absent epicardium		IAGP		N	RGD:5509061	20240229	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539357
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9322371
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375415
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0011825	decreased cell chemotaxis		IAGP		N	RGD:5509061	20160128	MGI			PMID:26034041
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0012299	hydropic allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:7587631
11481	Vcam1	vascular cell adhesion molecule 1	gene	MP:0014472	impaired B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:11257140
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:14584880
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17123805
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17099775
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976027
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385068
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532865
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11697802
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12089348
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14584880
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976027
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17123805
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11851870
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171393
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11851870
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12089348
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20240523	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962355
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532865
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962355
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962355
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20240523	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880407
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11851870
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880407
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001247	dermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11851870
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001247	dermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962355
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001283	sparse vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001340	abnormal eyelid morphology		IEA		N	RGD:5509061	20260402	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20240523	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17099775
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275288
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11851870
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880407
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385068
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385068
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385068
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385068
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11385068
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17551101
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275288
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275289
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11697802
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:14584880
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12089348
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17123805
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17123805
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003112	enlarged parathyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11851870
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:12089348
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:14584880
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976027
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275288
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976027
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17123805
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17099775
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003432	increased activity of parathyroid		IAGP		N	RGD:5509061	20141003	MGI			PMID:12089348
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003432	increased activity of parathyroid		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003432	increased activity of parathyroid		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003432	increased activity of parathyroid		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003493	parathyroid gland hyperplasia		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003639	abnormal response to vitamins		IAGP		N	RGD:5509061	20141003	MGI			PMID:12089348
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11851870
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17551101
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17974622
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11697802
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532865
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962355
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14584880
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17099775
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17551101
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005046	absent spleen white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20260402	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005401	abnormal fat-soluble vitamin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532865
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005401	abnormal fat-soluble vitamin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11697802
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12089348
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005522	increased circulating atrial natriuretic factor		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20260402	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005581	abnormal renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275289
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17099775
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005636	abnormal mineral homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976027
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0005636	abnormal mineral homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17099775
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275289
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006375	increased circulating angiotensinogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12089348
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962355
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008650	abnormal interleukin-1 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17959935
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639181
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0009257	dilated seminiferous tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11697802
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476050
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11697802
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14584880
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962355
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0010699	dilated hair follicle		IAGP		N	RGD:5509061	20181129	MGI			PMID:11851870
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0010699	dilated hair follicle		IAGP		N	RGD:5509061	20181129	MGI			PMID:9275211
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947295
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11697802
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0010926	increased osteoid volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0011221	decreased intestinal calcium absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687634
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12089348
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14584880
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17099775
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23389957
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0012175	flat face		IAGP		N	RGD:5509061	20141003	MGI			PMID:9241280
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0014965	increased heart enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:17275288
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20151001	MGI			PMID:25147982
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:15998839
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0030575	decreased hair follicle cell proliferation		IAGP		N	RGD:5509061	20181129	MGI			PMID:11851870
11484	Vdr	vitamin D (1,25-dihydroxyvitamin D3) receptor	gene	MP:0031232	increased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:12122115
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399150
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252526
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510575
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001138	abnormal uterine cervix squamous epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474617
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798202
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252526
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:22977222
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489957
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256442
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12628185
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510575
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002009	preneoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252526
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474617
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798202
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510575
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798202
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474617
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25417109
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798202
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651579
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340311
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003574	abnormal oviduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474617
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003597	increased epididymal cystadenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474617
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510575
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651579
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957870
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14604887
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252526
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0004967	abnormal kidney epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256442
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340311
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340311
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22977222
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957870
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798202
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957870
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651579
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798202
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489957
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256442
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0009043	increased pancreas adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340311
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474617
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:19252526
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16977322
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474617
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22977222
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22977222
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340311
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11171994
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256442
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651579
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252526
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011286	decreased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011336	abnormal kidney pelvis urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011372	decreased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957870
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18497742
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522651
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652107
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0014241	abnormal intracellular organelle physiology		IAGP		N	RGD:5509061	20230615	MGI			PMID:23541568
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0014606	dark spleen		IAGP		N	RGD:5509061	20250206	MGI			PMID:17992257
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:14500363
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:9256442
11485	Vhl	von Hippel-Lindau tumor suppressor	gene	MP:0031717	prolonged corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:22977222
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0001393	ataxia		IEA		N	RGD:5509061	20141003	MGI			
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20141003	MGI			
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20141003	MGI			
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20141003	MGI			
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0001505	hunched posture		IEA		N	RGD:5509061	20141003	MGI			
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0009476	enlarged cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21697765
11486	Vipr1	vasoactive intestinal peptide receptor 1	gene	MP:0031155	small intestine hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:21697765
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10221657
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10221657
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16361315
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0003134	increased late pro-B cell number		IAGP		N	RGD:5509061	20240404	MGI			PMID:12055243
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16361315
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16361315
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
11487	Vpreb1a	V-set pre-B cell surrogate light chain 1A	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
11489	Foxn1	forkhead box N1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202317
11489	Foxn1	forkhead box N1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202317
11489	Foxn1	forkhead box N1	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8629026
11489	Foxn1	forkhead box N1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:4929778
11489	Foxn1	forkhead box N1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5639157
11489	Foxn1	forkhead box N1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:721133
11489	Foxn1	forkhead box N1	gene	MP:0000322	increased granulocyte number		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15610506
11489	Foxn1	forkhead box N1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12893877
11489	Foxn1	forkhead box N1	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15610506
11489	Foxn1	forkhead box N1	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
11489	Foxn1	forkhead box N1	gene	MP:0000580	deformed nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:15610506
11489	Foxn1	forkhead box N1	gene	MP:0000580	deformed nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
11489	Foxn1	forkhead box N1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0000685	abnormal immune system morphology		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5784127
11489	Foxn1	forkhead box N1	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:721133
11489	Foxn1	forkhead box N1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:5784127
11489	Foxn1	forkhead box N1	gene	MP:0000694	spleen hypoplasia		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:721133
11489	Foxn1	forkhead box N1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5493276
11489	Foxn1	forkhead box N1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6698273
11489	Foxn1	forkhead box N1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8629026
11489	Foxn1	forkhead box N1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878619
11489	Foxn1	forkhead box N1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4007044
11489	Foxn1	forkhead box N1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7405870
11489	Foxn1	forkhead box N1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8629026
11489	Foxn1	forkhead box N1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053428
11489	Foxn1	forkhead box N1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20150319	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878619
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259083
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5639157
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5784127
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:721133
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8629026
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671685
11489	Foxn1	forkhead box N1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20160204	MGI			PMID:16972005
11489	Foxn1	forkhead box N1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:6698273
11489	Foxn1	forkhead box N1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20160324	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
11489	Foxn1	forkhead box N1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053428
11489	Foxn1	forkhead box N1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
11489	Foxn1	forkhead box N1	gene	MP:0000716	abnormal immune system cell morphology		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001211	wrinkled skin		IEA		N	RGD:5509061	20141003	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18064304
11489	Foxn1	forkhead box N1	gene	MP:0001274	curly vibrissae		IEA		N	RGD:5509061	20141003	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0001279	wavy vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001282	short vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001283	sparse vibrissae		IEA		N	RGD:5509061	20141003	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1287512
11489	Foxn1	forkhead box N1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001790	abnormal immune system physiology		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0001800	abnormal humoral immune response		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053428
11489	Foxn1	forkhead box N1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
11489	Foxn1	forkhead box N1	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20150205	MGI			PMID:24715454
11489	Foxn1	forkhead box N1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:4929778
11489	Foxn1	forkhead box N1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15922720
11489	Foxn1	forkhead box N1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001923	reduced female fertility		IEA		N	RGD:5509061	20141003	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671685
11489	Foxn1	forkhead box N1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0001935	decreased litter size		IEA		N	RGD:5509061	20141003	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0002032	increased sarcoma incidence		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12724523
11489	Foxn1	forkhead box N1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:1104226
11489	Foxn1	forkhead box N1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15922720
11489	Foxn1	forkhead box N1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7405870
11489	Foxn1	forkhead box N1	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12893877
11489	Foxn1	forkhead box N1	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20141003	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694130
11489	Foxn1	forkhead box N1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
11489	Foxn1	forkhead box N1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11038184
11489	Foxn1	forkhead box N1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5428870
11489	Foxn1	forkhead box N1	gene	MP:0002347	abnormal lymph node T cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5784127
11489	Foxn1	forkhead box N1	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5784127
11489	Foxn1	forkhead box N1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
11489	Foxn1	forkhead box N1	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15922720
11489	Foxn1	forkhead box N1	gene	MP:0002460	decreased immunoglobulin level		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:721133
11489	Foxn1	forkhead box N1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0002722	abnormal immune system organ morphology		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259083
11489	Foxn1	forkhead box N1	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259083
11489	Foxn1	forkhead box N1	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
11489	Foxn1	forkhead box N1	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
11489	Foxn1	forkhead box N1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:721133
11489	Foxn1	forkhead box N1	gene	MP:0003361	abnormal circulating gonadotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259083
11489	Foxn1	forkhead box N1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:18064304
11489	Foxn1	forkhead box N1	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10767081
11489	Foxn1	forkhead box N1	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202317
11489	Foxn1	forkhead box N1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0003811	abnormal hair cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878619
11489	Foxn1	forkhead box N1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:12893877
11489	Foxn1	forkhead box N1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:16791198
11489	Foxn1	forkhead box N1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:8629026
11489	Foxn1	forkhead box N1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671685
11489	Foxn1	forkhead box N1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20160204	MGI			PMID:16972005
11489	Foxn1	forkhead box N1	gene	MP:0003848	brittle hair		IEA		N	RGD:5509061	20141003	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0004125	abnormal venule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5784127
11489	Foxn1	forkhead box N1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9328433
11489	Foxn1	forkhead box N1	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:4929778
11489	Foxn1	forkhead box N1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694130
11489	Foxn1	forkhead box N1	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
11489	Foxn1	forkhead box N1	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8629026
11489	Foxn1	forkhead box N1	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16791198
11489	Foxn1	forkhead box N1	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20150205	MGI			PMID:24715454
11489	Foxn1	forkhead box N1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:4929778
11489	Foxn1	forkhead box N1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
11489	Foxn1	forkhead box N1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5428870
11489	Foxn1	forkhead box N1	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164958
11489	Foxn1	forkhead box N1	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
11489	Foxn1	forkhead box N1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0005150	cachexia		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1287512
11489	Foxn1	forkhead box N1	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:1729694
11489	Foxn1	forkhead box N1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:721133
11489	Foxn1	forkhead box N1	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:1287512
11489	Foxn1	forkhead box N1	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
11489	Foxn1	forkhead box N1	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878619
11489	Foxn1	forkhead box N1	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8629026
11489	Foxn1	forkhead box N1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
11489	Foxn1	forkhead box N1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
11489	Foxn1	forkhead box N1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
11489	Foxn1	forkhead box N1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0008101	lymph node hypoplasia		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
11489	Foxn1	forkhead box N1	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
11489	Foxn1	forkhead box N1	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20200813	MGI			PMID:27641500
11489	Foxn1	forkhead box N1	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
11489	Foxn1	forkhead box N1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
11489	Foxn1	forkhead box N1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
11489	Foxn1	forkhead box N1	gene	MP:0008600	decreased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
11489	Foxn1	forkhead box N1	gene	MP:0008732	reduced hair shaft melanin granule number		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0008737	abnormal spleen physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4929778
11489	Foxn1	forkhead box N1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:5784127
11489	Foxn1	forkhead box N1	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
11489	Foxn1	forkhead box N1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:1729694
11489	Foxn1	forkhead box N1	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694130
11489	Foxn1	forkhead box N1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694130
11489	Foxn1	forkhead box N1	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19955175
11489	Foxn1	forkhead box N1	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
11489	Foxn1	forkhead box N1	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053428
11489	Foxn1	forkhead box N1	gene	MP:0009801	abnormal hair cortex keratinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0010129	increased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072979
11489	Foxn1	forkhead box N1	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
11489	Foxn1	forkhead box N1	gene	MP:0010250	absent thymus cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0010268	decreased lymphoma incidence		IEA		N	RGD:5509061	20111116	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1729694
11489	Foxn1	forkhead box N1	gene	MP:0010681	abnormal hair follicle bulb morphology		IEA		N	RGD:5509061	20141003	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980117
11489	Foxn1	forkhead box N1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20141003	MGI			
11489	Foxn1	forkhead box N1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15141078
11489	Foxn1	forkhead box N1	gene	MP:0012399	short nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:15610506
11489	Foxn1	forkhead box N1	gene	MP:0012399	short nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
11489	Foxn1	forkhead box N1	gene	MP:0012400	nail dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15610506
11489	Foxn1	forkhead box N1	gene	MP:0012402	abnormal nail bed morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
11489	Foxn1	forkhead box N1	gene	MP:0012403	abnormal nail plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15610506
11489	Foxn1	forkhead box N1	gene	MP:0012403	abnormal nail plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
11489	Foxn1	forkhead box N1	gene	MP:0012405	abnormal nail matrix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15610506
11489	Foxn1	forkhead box N1	gene	MP:0012405	abnormal nail matrix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387539
11489	Foxn1	forkhead box N1	gene	MP:0013225	abnormal third pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053428
11489	Foxn1	forkhead box N1	gene	MP:0013587	absent thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0014130	thymus cyst		IAGP		N	RGD:5509061	20160324	MGI			PMID:14528302
11489	Foxn1	forkhead box N1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:1287512
11489	Foxn1	forkhead box N1	gene	MP:0020935	decreased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:1232464
11489	Foxn1	forkhead box N1	gene	MP:0020935	decreased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:185426
11489	Foxn1	forkhead box N1	gene	MP:0030605	abnormal corneocyte morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:2288204
11489	Foxn1	forkhead box N1	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:1287512
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11920562
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811581
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000776	abnormal inferior colliculus morphology		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2205396
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000798	abnormal frontal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2202907
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23444360
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2202907
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2205396
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:2202907
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:2205396
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000854	abnormal cerebellum development		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000867	abnormal cerebellum anterior vermis morphology		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2202907
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23444360
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23444360
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2202907
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0001504	abnormal posture		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2202907
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0001522	impaired swimming		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:2202907
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23444360
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0003312	abnormal locomotor coordination		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23444360
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:2205396
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004096	abnormal midbrain-hindbrain boundary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:2205396
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004097	abnormal cerebellar cortex morphology		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004143	muscle hypertonia		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004203	abnormal cranial flexure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2205396
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004205	absent hyoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811581
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004459	small alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004814	reduced linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23444360
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20221215	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20201022	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041177
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441669
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0008026	abnormal brain white matter morphology		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0008913	weaving		IEA		N	RGD:5509061	20111116	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23444360
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2205396
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2202907
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441669
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2202907
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:2205396
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441669
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23444360
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20141003	MGI			PMID:8555108
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0012516	absent metencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441669
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0012785	decreased rhombomere 1 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2205396
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0012785	decreased rhombomere 1 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23444360
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20171005	MGI			PMID:9353119
11491	Wnt1	wingless-type MMTV integration site family, member 1	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:9353119
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001679	thin apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001697	abnormal embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001710	absent amniotic folds		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0003895	increased ectoderm apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569130
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431243
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0011206	absent visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431240
11492	Wnt3	wingless-type MMTV integration site family, member 3	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:12569130
11493	Wt1	WT1 transcription factor	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
11493	Wt1	WT1 transcription factor	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20150625	MGI			PMID:24732380
11493	Wt1	WT1 transcription factor	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469569
11493	Wt1	WT1 transcription factor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220519	MGI			PMID:24009315
11493	Wt1	WT1 transcription factor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220519	MGI			PMID:24009315
11493	Wt1	WT1 transcription factor	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245160
11493	Wt1	WT1 transcription factor	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20161013	MGI			PMID:17071579
11493	Wt1	WT1 transcription factor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023660
11493	Wt1	WT1 transcription factor	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023660
11493	Wt1	WT1 transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023660
11493	Wt1	WT1 transcription factor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245160
11493	Wt1	WT1 transcription factor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220519	MGI			PMID:24009315
11493	Wt1	WT1 transcription factor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509792
11493	Wt1	WT1 transcription factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509792
11493	Wt1	WT1 transcription factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024052
11493	Wt1	WT1 transcription factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640141
11493	Wt1	WT1 transcription factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525726
11493	Wt1	WT1 transcription factor	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509181
11493	Wt1	WT1 transcription factor	gene	MP:0002212	abnormal secondary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509181
11493	Wt1	WT1 transcription factor	gene	MP:0002212	abnormal secondary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0002214	streak gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509181
11493	Wt1	WT1 transcription factor	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:23502960
11493	Wt1	WT1 transcription factor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509792
11493	Wt1	WT1 transcription factor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
11493	Wt1	WT1 transcription factor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509181
11493	Wt1	WT1 transcription factor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20150625	MGI			PMID:24732380
11493	Wt1	WT1 transcription factor	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509181
11493	Wt1	WT1 transcription factor	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20220519	MGI			PMID:24009315
11493	Wt1	WT1 transcription factor	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20220519	MGI			PMID:24009315
11493	Wt1	WT1 transcription factor	gene	MP:0003578	absent ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0003626	kidney medulla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20150625	MGI			PMID:24732380
11493	Wt1	WT1 transcription factor	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023660
11493	Wt1	WT1 transcription factor	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20161013	MGI			PMID:17071579
11493	Wt1	WT1 transcription factor	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20170302	MGI			PMID:27642710
11493	Wt1	WT1 transcription factor	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
11493	Wt1	WT1 transcription factor	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0004195	abnormal kidney calyx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245160
11493	Wt1	WT1 transcription factor	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023660
11493	Wt1	WT1 transcription factor	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509792
11493	Wt1	WT1 transcription factor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23502960
11493	Wt1	WT1 transcription factor	gene	MP:0005313	absent adrenal gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469569
11493	Wt1	WT1 transcription factor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509181
11493	Wt1	WT1 transcription factor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0005327	abnormal mesangial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0005327	abnormal mesangial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0005327	abnormal mesangial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0005644	agonadal		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:27642710
11493	Wt1	WT1 transcription factor	gene	MP:0006415	absent testes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0008138	absent podocyte foot process		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509792
11493	Wt1	WT1 transcription factor	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:24009315
11493	Wt1	WT1 transcription factor	gene	MP:0009322	increased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469569
11493	Wt1	WT1 transcription factor	gene	MP:0009323	abnormal spleen development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469569
11493	Wt1	WT1 transcription factor	gene	MP:0009362	abnormal primary ovarian follicle morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:24009315
11493	Wt1	WT1 transcription factor	gene	MP:0010118	abnormal intermediate mesoderm morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:27642710
11493	Wt1	WT1 transcription factor	gene	MP:0010294	increased kidney tumor incidence		IAGP		N	RGD:5509061	20150625	MGI			PMID:24732380
11493	Wt1	WT1 transcription factor	gene	MP:0010500	myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:26739565
11493	Wt1	WT1 transcription factor	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20170302	MGI			PMID:26739565
11493	Wt1	WT1 transcription factor	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469569
11493	Wt1	WT1 transcription factor	gene	MP:0010985	abnormal kidney mesenchyme morphology		IAGP		N	RGD:5509061	20150625	MGI			PMID:24732380
11493	Wt1	WT1 transcription factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469569
11493	Wt1	WT1 transcription factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509181
11493	Wt1	WT1 transcription factor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469569
11493	Wt1	WT1 transcription factor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525726
11493	Wt1	WT1 transcription factor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
11493	Wt1	WT1 transcription factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024052
11493	Wt1	WT1 transcription factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
11493	Wt1	WT1 transcription factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023660
11493	Wt1	WT1 transcription factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469569
11493	Wt1	WT1 transcription factor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20170302	MGI			PMID:26739565
11493	Wt1	WT1 transcription factor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20170302	MGI			PMID:27642710
11493	Wt1	WT1 transcription factor	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0011301	juxtaglomerular cell hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0011316	abnormal kidney interlobular artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0011366	absent metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
11493	Wt1	WT1 transcription factor	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0011411	abnormal gonadal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0011430	mesangiolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0011498	abnormal glomerular capsule parietal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0011500	decreased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0011868	podocyte microvillus transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0011871	podocyte hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10077614
11493	Wt1	WT1 transcription factor	gene	MP:0011871	podocyte hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0011871	podocyte hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797313
11493	Wt1	WT1 transcription factor	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20161013	MGI			PMID:17071579
11493	Wt1	WT1 transcription factor	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20170302	MGI			PMID:27642710
11493	Wt1	WT1 transcription factor	gene	MP:0012496	abnormal pleuropericardial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984617
11493	Wt1	WT1 transcription factor	gene	MP:0012515	abnormal heart apex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0012515	abnormal heart apex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8395349
11493	Wt1	WT1 transcription factor	gene	MP:0013310	abnormal adrenal gland development		IAGP		N	RGD:5509061	20141120	MGI			PMID:18040647
11493	Wt1	WT1 transcription factor	gene	MP:0014808	abnormal pleuroperitoneal fold morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:27642710
11493	Wt1	WT1 transcription factor	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:24009315
11493	Wt1	WT1 transcription factor	gene	MP:0031590	abnormal epicardium development		IAGP		N	RGD:5509061	20240229	MGI			PMID:19369973
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000161	scoliosis		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531011
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000550	abnormal forelimb morphology		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000556	abnormal hindlimb morphology		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9294146
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531386
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14642570
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531386
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810694
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8756720
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8756720
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9294146
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8756720
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531386
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8756720
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002145	abnormal T cell differentiation		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9294146
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20241121	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531011
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20241121	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0002981	increased liver weight		IEA		N	RGD:5509061	20241121	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716994
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531011
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531386
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9294146
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810694
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8756720
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0005270	abnormal zygomatic bone morphology		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8756720
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8756720
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008126	increased dendritic cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008167	increased B-1a cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008925	increased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531386
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0010463	aorta stenosis		IEA		N	RGD:5509061	20240523	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531386
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531011
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751807
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0013519	decreased CD4-positive NK T cell number		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0013522	decreased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20250508	MGI			
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:9294146
11495	Xrcc5	X-ray repair complementing 5	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:14642570
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11497	Ywhaq	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145769
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20160421	MGI			
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20160811	MGI			
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20211021	MGI			
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0009938	abnormal hippocampus granule cell morphology		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0010011	ectopic hippocampus pyramidal cells		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160505	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0014745	abnormal hippocampal mossy fiber infrapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:22124272
11498	Ywhaz	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22124272
11500	Yy1	YY1 transcription factor	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611997
11500	Yy1	YY1 transcription factor	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20181122	MGI			PMID:22570637
11500	Yy1	YY1 transcription factor	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10490658
11500	Yy1	YY1 transcription factor	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611997
11500	Yy1	YY1 transcription factor	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20141003	MGI			PMID:10490658
11500	Yy1	YY1 transcription factor	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10490658
11500	Yy1	YY1 transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611997
11500	Yy1	YY1 transcription factor	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20181122	MGI			PMID:22570637
11500	Yy1	YY1 transcription factor	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611997
11500	Yy1	YY1 transcription factor	gene	MP:0002174	abnormal gastrulation movements		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611997
11500	Yy1	YY1 transcription factor	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:22570637
11500	Yy1	YY1 transcription factor	gene	MP:0004880	lung cyst		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0005072	abnormal hair follicle melanin granule morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:22570637
11500	Yy1	YY1 transcription factor	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0008021	increased blastoma incidence		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0008238	abnormal dorsoventral coat patterning		IAGP		N	RGD:5509061	20181122	MGI			PMID:22570637
11500	Yy1	YY1 transcription factor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611997
11500	Yy1	YY1 transcription factor	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:22570637
11500	Yy1	YY1 transcription factor	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0010862	decreased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0010883	trachea stenosis		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0010949	decreased club cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611997
11500	Yy1	YY1 transcription factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10490658
11500	Yy1	YY1 transcription factor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611997
11500	Yy1	YY1 transcription factor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611997
11500	Yy1	YY1 transcription factor	gene	MP:0011113	abnormal airway basal cell morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0011124	increased primary ovarian follicle number		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0011130	absent tertiary ovarian follicles		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0011142	abnormal lung-associated mesenchyme development		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0011627	decreased skin pigmentation		IAGP		N	RGD:5509061	20181122	MGI			PMID:22570637
11500	Yy1	YY1 transcription factor	gene	MP:0012023	decreased melanocyte number		IAGP		N	RGD:5509061	20181122	MGI			PMID:22570637
11500	Yy1	YY1 transcription factor	gene	MP:0012197	impaired myofibroblast differentiation		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
11500	Yy1	YY1 transcription factor	gene	MP:0014200	abnormal respiratory epithelium physiology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0021106	abnormal secondary ovarian follicle morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0030002	increased lung apoptosis		IAGP		N	RGD:5509061	20170622	MGI			PMID:26329601
11500	Yy1	YY1 transcription factor	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220609	MGI			PMID:21123818
11500	Yy1	YY1 transcription factor	gene	MP:0031436	decreased copulatory plug deposition		IAGP		N	RGD:5509061	20220922	MGI			PMID:21123818
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IEA		N	RGD:5509061	20111116	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001606	impaired hematopoiesis		IEA		N	RGD:5509061	20161201	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17767948
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9208839
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9208839
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794398
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001828	abnormal T cell activation		IEA		N	RGD:5509061	20111116	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567635
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17767948
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794398
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794398
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9208839
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17767948
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002935	chronic joint inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002936	joint swelling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514605
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0003189	fused joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IEA		N	RGD:5509061	20111116	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0003944	abnormal T cell subpopulation ratio		IEA		N	RGD:5509061	20111116	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0004917	abnormal T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0004972	abnormal regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005002	abnormal T cell clonal deletion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17767948
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9208839
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750595
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514605
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514605
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008070	absent T cells		IEA		N	RGD:5509061	20111116	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567635
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17767948
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14647385
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17767948
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008233	abnormal pro-B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18356083
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17767948
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008501	increased IgG2b level		IEA		N	RGD:5509061	20111116	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794398
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514605
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514605
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841086
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9794398
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20180215	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20180215	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20151112	MGI			
11501	Zap70	zeta-chain (TCR) associated protein kinase	gene	MP:0030795	joint dislocation		IAGP		N	RGD:5509061	20181018	MGI			PMID:14647385
11502	Rnf112	ring finger protein 112	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20161013	MGI			PMID:26212327
11502	Rnf112	ring finger protein 112	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
11502	Rnf112	ring finger protein 112	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26212327
11502	Rnf112	ring finger protein 112	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
11502	Rnf112	ring finger protein 112	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20161013	MGI			PMID:26212327
11502	Rnf112	ring finger protein 112	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20161013	MGI			PMID:26212327
11502	Rnf112	ring finger protein 112	gene	MP:0021018	decreased dendritic spine number		IAGP		N	RGD:5509061	20211014	MGI			PMID:26212327
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893599
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287387
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893599
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20211028	MGI			PMID:27511108
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893599
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0005237	abnormal olfactory tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20250508	MGI			
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20211028	MGI			PMID:27511108
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23431164
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0008129	absent brain internal capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0008232	abnormal cingulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21893599
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20210128	MGI			
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0010654	slow Wallerian degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287387
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0010859	abnormal anterior commissure pars anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0010860	abnormal anterior commissure pars posterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17108173
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
11503	Map3k12	mitogen-activated protein kinase kinase kinase 12	gene	MP:0014553	decreased neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:17108173
11522747	Eae41_m	experimental allergic encephalomyelitis susceptibility 41 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20160805	MGI		Created by mouse qtl pipeline	PMID:12517969
11522747	Eae41_m	experimental allergic encephalomyelitis susceptibility 41 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160805	MGI		Created by mouse qtl pipeline	PMID:12517969
11522747	Eae41_m	experimental allergic encephalomyelitis susceptibility 41 (mouse)	qtl	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20160811	MGI			PMID:12517969
12436784	Bend2	BEN domain containing 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220804	MGI			PMID:35613276
12436784	Bend2	BEN domain containing 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220804	MGI			PMID:35613276
12436784	Bend2	BEN domain containing 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220804	MGI			PMID:35613276
12436784	Bend2	BEN domain containing 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20220804	MGI			PMID:35613276
12436784	Bend2	BEN domain containing 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220804	MGI			PMID:35613276
12436820	S2bpcox16	synaptojanin 2 binding protein Cox16 readthrough	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20231207	MGI			
12436820	S2bpcox16	synaptojanin 2 binding protein Cox16 readthrough	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
12436820	S2bpcox16	synaptojanin 2 binding protein Cox16 readthrough	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
12436820	S2bpcox16	synaptojanin 2 binding protein Cox16 readthrough	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20240523	MGI			
12879483	Asp1_m	audiogenic seizure prone 1 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20170427	MGI			PMID:7399258
12879483	Asp1_m	audiogenic seizure prone 1 (mouse)	qtl	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20170427	MGI			PMID:7399258
12879483	Asp1_m	audiogenic seizure prone 1 (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20170427	MGI			PMID:7399258
12879483	Asp1_m	audiogenic seizure prone 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20170421	MGI		Created by mouse qtl pipeline	PMID:7399258
12879483	Asp1_m	audiogenic seizure prone 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20170421	MGI		Created by mouse qtl pipeline	PMID:7399258
12879483	Asp1_m	audiogenic seizure prone 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20170421	MGI		Created by mouse qtl pipeline	PMID:7399258
12879484	Asp2_m	audiogenic seizure prone 2 (mouse)	qtl	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20170427	MGI			PMID:2052619
12879484	Asp2_m	audiogenic seizure prone 2 (mouse)	qtl	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20170427	MGI			PMID:5698855
12879484	Asp2_m	audiogenic seizure prone 2 (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20170427	MGI			PMID:2052619
12879484	Asp2_m	audiogenic seizure prone 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20170421	MGI		Created by mouse qtl pipeline	PMID:5698855|PMID:5527661
12879484	Asp2_m	audiogenic seizure prone 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20170421	MGI		Created by mouse qtl pipeline	PMID:5698855|PMID:5527661
12879484	Asp2_m	audiogenic seizure prone 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20170421	MGI		Created by mouse qtl pipeline	PMID:5698855|PMID:5527661
12879484	Asp2_m	audiogenic seizure prone 2 (mouse)	qtl	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:2052619
12904746	Litsq1_m	litter size QTL 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20170519	MGI		Created by mouse qtl pipeline	PMID:18239664
12910120	Mahl_m	modifier of age related hearing loss (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20170616	MGI		Created by mouse qtl pipeline	PMID:28287619
12910120	Mahl_m	modifier of age related hearing loss (mouse)	qtl	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20170615	MGI			PMID:28287619
12910120	Mahl_m	modifier of age related hearing loss (mouse)	qtl	MP:0005377	hearing/vestibular/ear phenotype		IEA		N	RGD:704405	20170616	MGI		Created by mouse qtl pipeline	PMID:28287619
12910120	Mahl_m	modifier of age related hearing loss (mouse)	qtl	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20170615	MGI			PMID:28287619
1300528	Ssial3_m	susceptibility to sialadenitis 3 (mouse)	qtl	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11937580
1300528	Ssial3_m	susceptibility to sialadenitis 3 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1300528	Ssial3_m	susceptibility to sialadenitis 3 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1300528	Ssial3_m	susceptibility to sialadenitis 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1300529	Idd9.3_m	insulin dependent diabetes susceptibility 9.3 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10933399
1300529	Idd9.3_m	insulin dependent diabetes susceptibility 9.3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10933399
1300530	Livq2_m	percent liver QTL 2 (mouse)	qtl	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1300530	Livq2_m	percent liver QTL 2 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1300530	Livq2_m	percent liver QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10353911
1300532	Tbs2_m	tuberculosis severity 2 (mouse)	qtl	MP:0001263	weight loss		IAGP		N	RGD:5509061	20111116	MGI			PMID:12496157
1300532	Tbs2_m	tuberculosis severity 2 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12496157
1300532	Tbs2_m	tuberculosis severity 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353873
1300532	Tbs2_m	tuberculosis severity 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353873
1300533	Aem3_m	anti-erythrocyte autoantibody modifier 3 (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10607744
1300533	Aem3_m	anti-erythrocyte autoantibody modifier 3 (mouse)	qtl	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10607744
1300533	Aem3_m	anti-erythrocyte autoantibody modifier 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10607744
1300534	Bmd15_m	bone mineral density 15 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11450694
1300534	Bmd15_m	bone mineral density 15 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1300535	Char3_m	P. chabaudi malaria resistance QTL 3 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10630291
1300535	Char3_m	P. chabaudi malaria resistance QTL 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15170228|PMID:10630291
1300535	Char3_m	P. chabaudi malaria resistance QTL 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:10630291
1300537	Ap3q_m	alcohol preference 3 QTL (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:9726281
1300537	Ap3q_m	alcohol preference 3 QTL (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9726281
1300538	Disso2_m	dissociation of activity 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11381025
1300538	Disso2_m	dissociation of activity 2 (mouse)	qtl	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:11381025
1300540	Igfbp3q1_m	insulin-like growth factor binding protein 3 QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11292658
1300540	Igfbp3q1_m	insulin-like growth factor binding protein 3 QTL 1 (mouse)	qtl	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11292658
1300542	Lbm7_m	lean body mass 7 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1300542	Lbm7_m	lean body mass 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1300544	Hypn_m	hyperinsulinemia (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12765967
1300544	Hypn_m	hyperinsulinemia (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561960
1300544	Hypn_m	hyperinsulinemia (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12765967
1300545	Lifespan3_m	life span 3 (mouse)	qtl	MP:0001661	extended life span		IAGP		N	RGD:5509061	20111116	MGI			PMID:11773201
1300545	Lifespan3_m	life span 3 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11773201
1300547	Cypr2_m	cytokine production 2 (mouse)	qtl	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:9887350
1300547	Cypr2_m	cytokine production 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9887350
1300548	Adaz1_m	anti-dsDNA antibody production in NZM 1 (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11513551
1300548	Adaz1_m	anti-dsDNA antibody production in NZM 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11513551
1300549	Bbaa17_m	B. burgdorferi-associated arthritis 17 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1300549	Bbaa17_m	B. burgdorferi-associated arthritis 17 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1300550	Szv2_m	seizure severity 2 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:9069121
1300550	Szv2_m	seizure severity 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9069121
1300550	Szv2_m	seizure severity 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9069121
1300551	Lprm3_m	lymphoproliferation modifier 3 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9403730
1300551	Lprm3_m	lymphoproliferation modifier 3 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9403730
1300551	Lprm3_m	lymphoproliferation modifier 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9403730
1300552	Lrnx8_m	learning-contextual 8 (mouse)	qtl	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:9354800
1300552	Lrnx8_m	learning-contextual 8 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9354800
1300553	Athsq1_m	atherosclerosis susceptibility QTL 1 (mouse)	qtl	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11438740
1300553	Athsq1_m	atherosclerosis susceptibility QTL 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:17641228|PMID:11438740
1300553	Athsq1_m	atherosclerosis susceptibility QTL 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20150206	MGI		Created by mouse qtl pipeline	PMID:11438740
1300554	Giq1_m	glucose intolerance QTL 1 (mouse)	qtl	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:12439655
1300554	Giq1_m	glucose intolerance QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12439655
1300556	Cia6_m	collagen induced arthritis QTL 6 (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10453039
1300556	Cia6_m	collagen induced arthritis QTL 6 (mouse)	qtl	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10453039
1300556	Cia6_m	collagen induced arthritis QTL 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10453039
1300558	Bw5_m	body weight QTL 5 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9725853
1300558	Bw5_m	body weight QTL 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089|PMID:9725853
1300558	Bw5_m	body weight QTL 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:9725853
1300560	Tgl1_m	triglyceride level 1 (mouse)	qtl	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11473059
1300560	Tgl1_m	triglyceride level 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11473059
1300561	Heal7_m	wound healing/regeneration 7 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:9751744
1300561	Heal7_m	wound healing/regeneration 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777|PMID:9751744
1300561	Heal7_m	wound healing/regeneration 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:9751744
1300563	Pgia5_m	proteoglycan induced arthritis 5 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1300563	Pgia5_m	proteoglycan induced arthritis 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997|PMID:15084914
1300563	Pgia5_m	proteoglycan induced arthritis 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:10615997
1300564	Hlq5_m	heat loss QTL 5 (mouse)	qtl	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1300564	Hlq5_m	heat loss QTL 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1300565	Batq1_m	brown fat QTL 1 (mouse)	qtl	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1300565	Batq1_m	brown fat QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1300567	Bwq3_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11515095
1300567	Bwq3_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11515095
1300568	Hdl1_m	high density lipoprotein (HDL) level 1 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11108726
1300568	Hdl1_m	high density lipoprotein (HDL) level 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11108726|PMID:12588951
1300568	Hdl1_m	high density lipoprotein (HDL) level 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:11108726
1300569	Eae6b_m	susceptibility to experimental allergic encephalomyelitis 6b (mouse)	qtl	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10438970
1300569	Eae6b_m	susceptibility to experimental allergic encephalomyelitis 6b (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9712054
1300573	Elsgp2_m	elevated serum gp70 2 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10903778
1300573	Elsgp2_m	elevated serum gp70 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10903778
1300574	Im2_m	immunoregulatory 2 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11058581
1300574	Im2_m	immunoregulatory 2 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:8962125
1300574	Im2_m	immunoregulatory 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11058581
1300576	Yaail_m	Yaa interacting locus (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9862363
1300576	Yaail_m	Yaa interacting locus (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9862363
1300576	Yaail_m	Yaa interacting locus (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9862363
1300576	Yaail_m	Yaa interacting locus (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9862363
1300577	Capsq1_m	capsaicin sensitivity related QTL 1 (mouse)	qtl	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14499433
1300577	Capsq1_m	capsaicin sensitivity related QTL 1 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14499433
1300578	Cd8ts3_m	CD8 T cell subset 3 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300578	Cd8ts3_m	CD8 T cell subset 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300578	Cd8ts3_m	CD8 T cell subset 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300578	Cd8ts3_m	CD8 T cell subset 3 (mouse)	qtl	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300579	Thypr1_m	thymocyte proliferative response 1 (mouse)	qtl	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12044964
1300579	Thypr1_m	thymocyte proliferative response 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12044964
1300579	Thypr1_m	thymocyte proliferative response 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12044964
1300579	Thypr1_m	thymocyte proliferative response 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12044964
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0001785	edema		IAGP		N	RGD:5509061	20111116	MGI			PMID:15814738
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15814738
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15814738
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20111116	MGI			PMID:15814738
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20111116	MGI			PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15814738
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15814738
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15814738
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15814738
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15814738
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20170127	MGI		Created by mouse qtl pipeline	PMID:22371393|PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20170127	MGI		Created by mouse qtl pipeline	PMID:22371393|PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20170127	MGI		Created by mouse qtl pipeline	PMID:22371393|PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20170127	MGI		Created by mouse qtl pipeline	PMID:22371393|PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1300580	Lbw2_m	lupus NZB x NZW 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20170127	MGI		Created by mouse qtl pipeline	PMID:22371393|PMID:7937857
1300581	Tbrs1_m	tuberculosis resistance 1 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11197687
1300581	Tbrs1_m	tuberculosis resistance 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11197687
1300583	Pbwg2_m	postnatal body weight growth 2 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1300583	Pbwg2_m	postnatal body weight growth 2 (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15056934
1300583	Pbwg2_m	postnatal body weight growth 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15056934
1300585	Pgia12_m	proteoglycan induced arthritis 12 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1300585	Pgia12_m	proteoglycan induced arthritis 12 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997|PMID:15084914
1300585	Pgia12_m	proteoglycan induced arthritis 12 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:10615997
1300586	Cdcs5_m	cytokine deficiency colitis susceptibility 5 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11707574
1300586	Cdcs5_m	cytokine deficiency colitis susceptibility 5 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1300586	Cdcs5_m	cytokine deficiency colitis susceptibility 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1300591	Pas3_m	pulmonary adenoma susceptibility 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7894154|PMID:7813906
1300592	Pcyts5_m	plasmacytoma susceptibility 5 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12149518
1300592	Pcyts5_m	plasmacytoma susceptibility 5 (mouse)	qtl	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12149518
1300593	Skull4_m	skull morphology 4 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1300593	Skull4_m	skull morphology 4 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300593	Skull4_m	skull morphology 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300594	Eae2_m	susceptibility to experimental allergic encephalomyelitis 2 (mouse)	qtl	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1300594	Eae2_m	susceptibility to experimental allergic encephalomyelitis 2 (mouse)	qtl	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1300594	Eae2_m	susceptibility to experimental allergic encephalomyelitis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7545492
1300594	Eae2_m	susceptibility to experimental allergic encephalomyelitis 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7545492
1300597	Skull14_m	skull morphology 14 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1300597	Skull14_m	skull morphology 14 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300597	Skull14_m	skull morphology 14 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300598	Disso1_m	dissociation of activity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11381025
1300598	Disso1_m	dissociation of activity 1 (mouse)	qtl	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:11381025
1300600	Hdl2_m	high density lipoprotein (HDL) level 2 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11108726
1300600	Hdl2_m	high density lipoprotein (HDL) level 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11108726
1300602	Eye2_m	eye weight 2 (mouse)	qtl	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10102277
1300602	Eye2_m	eye weight 2 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10102277
1300603	Cd8ts2_m	CD8 T cell subset 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300603	Cd8ts2_m	CD8 T cell subset 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300603	Cd8ts2_m	CD8 T cell subset 2 (mouse)	qtl	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300604	Mndl1_m	mandible length 1 (mouse)	qtl	MP:0000088	short mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:12161465
1300604	Mndl1_m	mandible length 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:12161465
1300604	Mndl1_m	mandible length 1 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12161465
1300604	Mndl1_m	mandible length 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12161465
1300605	El5_m	epilepsy 5 (mouse)	qtl	MP:0002064	seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:8747920
1300605	El5_m	epilepsy 5 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8747920
1300605	El5_m	epilepsy 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8747920
1300606	Axtofa6_m	anxiety-open field activity 6 (mouse)	qtl	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14990867
1300606	Axtofa6_m	anxiety-open field activity 6 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769|PMID:14990867
1300606	Axtofa6_m	anxiety-open field activity 6 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11493566|PMID:11454769
1300607	Tnbs2_m	tri-nitrobenzene sulfonic acid susceptible 2 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300607	Tnbs2_m	tri-nitrobenzene sulfonic acid susceptible 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300607	Tnbs2_m	tri-nitrobenzene sulfonic acid susceptible 2 (mouse)	qtl	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12145808
1300607	Tnbs2_m	tri-nitrobenzene sulfonic acid susceptible 2 (mouse)	qtl	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:12145808
1300611	Tlln_m	tail length (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:10051315
1300611	Tlln_m	tail length (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:17541685
1300611	Tlln_m	tail length (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10051315
1300612	Idd13_m	insulin dependent diabetes susceptibility 13 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7931087
1300612	Idd13_m	insulin dependent diabetes susceptibility 13 (mouse)	qtl	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1300612	Idd13_m	insulin dependent diabetes susceptibility 13 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12759418|PMID:7931087
1300612	Idd13_m	insulin dependent diabetes susceptibility 13 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12759418|PMID:7931087
1300612	Idd13_m	insulin dependent diabetes susceptibility 13 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:12759418|PMID:7931087
1300612	Idd13_m	insulin dependent diabetes susceptibility 13 (mouse)	qtl	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1300613	Pcyts4_m	plasmacytoma susceptibility 4 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12149518
1300613	Pcyts4_m	plasmacytoma susceptibility 4 (mouse)	qtl	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12149518
1300614	Afw6_m	abdominal fat weight QTL 6 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089|PMID:9725853
1300615	Hpic4_m	haloperidol induced catalepsy 4 (mouse)	qtl	MP:0002822	catalepsy		IAGP		N	RGD:5509061	20111116	MGI			PMID:10454512
1300615	Hpic4_m	haloperidol induced catalepsy 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11166067
1300615	Hpic4_m	haloperidol induced catalepsy 4 (mouse)	qtl	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20111116	MGI			PMID:10454512
1300617	Naq1_m	nurturing ability QTL 1 (mouse)	qtl	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11869186
1300617	Naq1_m	nurturing ability QTL 1 (mouse)	qtl	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20111116	MGI			PMID:15472464
1300617	Naq1_m	nurturing ability QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11869186
1300619	Cdcs1_m	cytokine deficiency colitis susceptibility 1 (mouse)	qtl	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11707574
1300619	Cdcs1_m	cytokine deficiency colitis susceptibility 1 (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11707574
1300619	Cdcs1_m	cytokine deficiency colitis susceptibility 1 (mouse)	qtl	MP:0002816	colitis		IAGP		N	RGD:5509061	20150702	MGI			PMID:11707574
1300619	Cdcs1_m	cytokine deficiency colitis susceptibility 1 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1300619	Cdcs1_m	cytokine deficiency colitis susceptibility 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1300621	Tpnr1_m	thermal pain response 1 (mouse)	qtl	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20111116	MGI			PMID:9150302
1300621	Tpnr1_m	thermal pain response 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9150302
1300621	Tpnr1_m	thermal pain response 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9150302
1300622	Cfld1_m	cystic fibrosis lung disease 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:12461645
1300622	Cfld1_m	cystic fibrosis lung disease 1 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12461645
1300622	Cfld1_m	cystic fibrosis lung disease 1 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12461645
1300624	Insq7_m	insulin QTL 7 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10871196
1300624	Insq7_m	insulin QTL 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10871196
1300625	Cosz2_m	cocaine seizure 2 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:10734168
1300625	Cosz2_m	cocaine seizure 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10734168
1300625	Cosz2_m	cocaine seizure 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10734168
1300626	Idd9.2_m	insulin dependent diabetes susceptibility 9.2 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10933399
1300626	Idd9.2_m	insulin dependent diabetes susceptibility 9.2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10933399
1300627	Sluc26_m	susceptibility to lung cancer 26 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1300627	Sluc26_m	susceptibility to lung cancer 26 (mouse)	qtl	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300627	Sluc26_m	susceptibility to lung cancer 26 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300627	Sluc26_m	susceptibility to lung cancer 26 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300627	Sluc26_m	susceptibility to lung cancer 26 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11584065
1300628	Lgth6_m	body length 6 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1300628	Lgth6_m	body length 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:12185457
1300628	Lgth6_m	body length 6 (mouse)	qtl	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:16254318
1300629	Fbgl2_m	fasting blood glucose 2 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11473059
1300629	Fbgl2_m	fasting blood glucose 2 (mouse)	qtl	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20111116	MGI			PMID:15769825
1300629	Fbgl2_m	fasting blood glucose 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11473059
1300629	Fbgl2_m	fasting blood glucose 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11473059
1300630	Livq3_m	percent liver QTL 3 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1300630	Livq3_m	percent liver QTL 3 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1300632	Loca2_m	locomotor activity 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14694905
1300632	Loca2_m	locomotor activity 2 (mouse)	qtl	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:14694905
1300633	Cdcs7_m	cytokine deficiency colitis susceptibility 7 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12213197
1300633	Cdcs7_m	cytokine deficiency colitis susceptibility 7 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12213197
1300633	Cdcs7_m	cytokine deficiency colitis susceptibility 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12213197
1300634	Sluc25_m	susceptibility to lung cancer 25 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1300634	Sluc25_m	susceptibility to lung cancer 25 (mouse)	qtl	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300634	Sluc25_m	susceptibility to lung cancer 25 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300634	Sluc25_m	susceptibility to lung cancer 25 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11584065
1300637	Batq2_m	brown fat QTL 2 (mouse)	qtl	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1300637	Batq2_m	brown fat QTL 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1300638	Im7_m	immunoregulatory 7 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:8962125
1300638	Im7_m	immunoregulatory 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8962125
1300644	Fob3_m	F-line obesity QTL 3 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:10602985
1300644	Fob3_m	F-line obesity QTL 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10602985
1300645	Alcp1_m	alcohol preference locus 1 (mouse)	qtl	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:8640219
1300645	Alcp1_m	alcohol preference locus 1 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:15547446
1300645	Alcp1_m	alcohol preference locus 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10443995|PMID:9880657
1300645	Alcp1_m	alcohol preference locus 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:9880657
1300646	Rapop4_m	radiation-induced apoptosis 4 (mouse)	qtl	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9367689
1300646	Rapop4_m	radiation-induced apoptosis 4 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9367689
1300647	Nktcn2_m	natural killer T cell numbers 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12960309
1300647	Nktcn2_m	natural killer T cell numbers 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12960309
1300647	Nktcn2_m	natural killer T cell numbers 2 (mouse)	qtl	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12960309
1300648	Dbsty4_m	diabesity 4 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11042154
1300648	Dbsty4_m	diabesity 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11042154
1300650	Bw18_m	body weight QTL 18 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1300650	Bw18_m	body weight QTL 18 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1300650	Bw18_m	body weight QTL 18 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11109545
1300651	Pcyts3_m	plasmacytoma susceptibility 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12149518
1300651	Pcyts3_m	plasmacytoma susceptibility 3 (mouse)	qtl	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12149518
1300652	Vmbic9_m	ventral midbrain iron content 9 (mouse)	qtl	MP:0000192	abnormal mineral level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16910173
1300652	Vmbic9_m	ventral midbrain iron content 9 (mouse)	qtl	MP:0003952	abnormal copper level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16910173
1300652	Vmbic9_m	ventral midbrain iron content 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14744041
1300652	Vmbic9_m	ventral midbrain iron content 9 (mouse)	qtl	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:16910173
1300653	Imh1_m	IgM hypergammaglobulinemia 1 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:6334582
1300653	Imh1_m	IgM hypergammaglobulinemia 1 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:6334582
1300653	Imh1_m	IgM hypergammaglobulinemia 1 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:7696204
1300653	Imh1_m	IgM hypergammaglobulinemia 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:6334582
1300653	Imh1_m	IgM hypergammaglobulinemia 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:6334582
1300655	Nidds_m	non-insulin-dependent diabetes mellitus in SJL (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10969845
1300655	Nidds_m	non-insulin-dependent diabetes mellitus in SJL (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:10969845
1300655	Nidds_m	non-insulin-dependent diabetes mellitus in SJL (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12107726
1300655	Nidds_m	non-insulin-dependent diabetes mellitus in SJL (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12107726
1300655	Nidds_m	non-insulin-dependent diabetes mellitus in SJL (mouse)	qtl	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10969845
1300655	Nidds_m	non-insulin-dependent diabetes mellitus in SJL (mouse)	qtl	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12107726
1300655	Nidds_m	non-insulin-dependent diabetes mellitus in SJL (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12107726
1300655	Nidds_m	non-insulin-dependent diabetes mellitus in SJL (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12107726
1300655	Nidds_m	non-insulin-dependent diabetes mellitus in SJL (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12107726
1300658	Cara1_m	carcass ash in high growth mice 1 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1300658	Cara1_m	carcass ash in high growth mice 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1300659	Pcd8ts1_m	p-glycoprotein positive CD8 T cell subset 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300659	Pcd8ts1_m	p-glycoprotein positive CD8 T cell subset 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300659	Pcd8ts1_m	p-glycoprotein positive CD8 T cell subset 1 (mouse)	qtl	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300663	Start2_m	startle response 2 (mouse)	qtl	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1300663	Start2_m	startle response 2 (mouse)	qtl	MP:0005377	hearing/vestibular/ear phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1300663	Start2_m	startle response 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1300665	Pbw2_m	pentobarbital withdrawal QTL 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11978849
1300665	Pbw2_m	pentobarbital withdrawal QTL 2 (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11978849
1300665	Pbw2_m	pentobarbital withdrawal QTL 2 (mouse)	qtl	MP:0009776	decreased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11978849
1300665	Pbw2_m	pentobarbital withdrawal QTL 2 (mouse)	qtl	MP:0009776	decreased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15208631
1300667	Lbw4_m	lupus NZB x NZW 4 (mouse)	qtl	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9922399
1300667	Lbw4_m	lupus NZB x NZW 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9922399|PMID:12215897
1300667	Lbw4_m	lupus NZB x NZW 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:7937857
1300667	Lbw4_m	lupus NZB x NZW 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:9922399|PMID:12215897
1300667	Lbw4_m	lupus NZB x NZW 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:7937857
1300670	Sluc19_m	susceptibility to lung cancer 19 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1300670	Sluc19_m	susceptibility to lung cancer 19 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300672	Hdlq26_m	HDL QTL 26 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1300672	Hdlq26_m	HDL QTL 26 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1300673	Cosz1_m	cocaine seizure 1 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:10734168
1300673	Cosz1_m	cocaine seizure 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10734168
1300673	Cosz1_m	cocaine seizure 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10734168
1300674	Nidd3n_m	non-insulin-dependent diabetes mellitus 3 in NSY (mouse)	qtl	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:10331425
1300674	Nidd3n_m	non-insulin-dependent diabetes mellitus 3 in NSY (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331425
1300675	Laq1_m	lupus associated arthritis quantitative trait locus 1 (mouse)	qtl	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1300675	Laq1_m	lupus associated arthritis quantitative trait locus 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449705
1300676	Prdt2_m	prion disease incubation time 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11353827
1300676	Prdt2_m	prion disease incubation time 2 (mouse)	qtl	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11353827
1300677	Bmd9_m	bone mineral density 9 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16355279|PMID:11450694
1300677	Bmd9_m	bone mineral density 9 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:11450694
1300677	Bmd9_m	bone mineral density 9 (mouse)	qtl	MP:0021186	decreased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:11450694
1300677	Bmd9_m	bone mineral density 9 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:16355279
1300679	Nociq2_m	nociceptive sensitivity inflammatory QTL 2 (mouse)	qtl	MP:0002735	abnormal chemical nociception		IAGP		N	RGD:5509061	20111116	MGI			PMID:11973013
1300679	Nociq2_m	nociceptive sensitivity inflammatory QTL 2 (mouse)	qtl	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11973013
1300679	Nociq2_m	nociceptive sensitivity inflammatory QTL 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973013
1300679	Nociq2_m	nociceptive sensitivity inflammatory QTL 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973013
1300685	Scc5_m	colon tumor susceptibility 5 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8944029
1300685	Scc5_m	colon tumor susceptibility 5 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:14562056
1300685	Scc5_m	colon tumor susceptibility 5 (mouse)	qtl	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8944029
1300685	Scc5_m	colon tumor susceptibility 5 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:8944029
1300686	C10bw4_m	castaneus 10 week body weight 4 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11003694
1300686	C10bw4_m	castaneus 10 week body weight 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11003694
1300688	Nidd2k_m	Nidd2 on KK-A<y> (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12115031
1300688	Nidd2k_m	Nidd2 on KK-A<y> (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12115031
1300688	Nidd2k_m	Nidd2 on KK-A<y> (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12115031
1300688	Nidd2k_m	Nidd2 on KK-A<y> (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12115031
1300688	Nidd2k_m	Nidd2 on KK-A<y> (mouse)	qtl	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20111116	MGI			PMID:12115031
1300689	Dob1_m	Dietary obesity 1 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:8000138
1300689	Dob1_m	Dietary obesity 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8000138
1300691	Skmw3_m	skeletal muscle weight 3 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14679300
1300691	Skmw3_m	skeletal muscle weight 3 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14679300
1300692	Blmpf1_m	bleomycin-induced pulmonary fibrosis 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:12140188
1300692	Blmpf1_m	bleomycin-induced pulmonary fibrosis 1 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12140188
1300692	Blmpf1_m	bleomycin-induced pulmonary fibrosis 1 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12140188
1300694	Tmevd7_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 7 (mouse)	qtl	MP:0000921	demyelination		IAGP		N	RGD:5509061	20111116	MGI			PMID:12663542
1300694	Tmevd7_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 7 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12663542
1300696	Bpq2_m	blood pressure QTL 2 (mouse)	qtl	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20111116	MGI			PMID:11161799
1300696	Bpq2_m	blood pressure QTL 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11161799
1300697	Sle2_m	systemic lupus erythmatosus susceptibility 2 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7889410
1300697	Sle2_m	systemic lupus erythmatosus susceptibility 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7889410
1300697	Sle2_m	systemic lupus erythmatosus susceptibility 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7889410
1300697	Sle2_m	systemic lupus erythmatosus susceptibility 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7889410
1300697	Sle2_m	systemic lupus erythmatosus susceptibility 2 (mouse)	qtl	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:18607347
1300697	Sle2_m	systemic lupus erythmatosus susceptibility 2 (mouse)	qtl	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:18607347
1300700	Sprol1_m	spontaneous proliferation 1 (mouse)	qtl	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:10384038
1300700	Sprol1_m	spontaneous proliferation 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10384038
1300700	Sprol1_m	spontaneous proliferation 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10384038
1300701	Cd8ts1_m	CD8 T cell subset 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300701	Cd8ts1_m	CD8 T cell subset 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300701	Cd8ts1_m	CD8 T cell subset 1 (mouse)	qtl	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300702	Fcsa4_m	femoral cross-sectional area 4 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1300702	Fcsa4_m	femoral cross-sectional area 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1300702	Fcsa4_m	femoral cross-sectional area 4 (mouse)	qtl	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12369778
1300704	Cia3_m	collagen induced arthritis QTL 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10051620|PMID:19234197
1300704	Cia3_m	collagen induced arthritis QTL 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10051620|PMID:19234197
1300705	Lipq2_m	lipoprotein QTL 2 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14722362
1300705	Lipq2_m	lipoprotein QTL 2 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14722362
1300705	Lipq2_m	lipoprotein QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14722362
1300708	Pbwm_m	pentobarbital withdrawal modifier (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529278
1300708	Pbwm_m	pentobarbital withdrawal modifier (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529278
1300710	Pcd4ts2_m	p-glycoprotein positive CD4 T cell subset 2 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300710	Pcd4ts2_m	p-glycoprotein positive CD4 T cell subset 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300710	Pcd4ts2_m	p-glycoprotein positive CD4 T cell subset 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300712	El2_m	epilepsy 2 (mouse)	qtl	MP:0002064	seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:17010098
1300712	El2_m	epilepsy 2 (mouse)	qtl	MP:0002064	seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:1871601
1300712	El2_m	epilepsy 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1871601
1300712	El2_m	epilepsy 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1871601
1300714	Idd7_m	insulin dependent diabetes susceptibility 7 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7556956
1300714	Idd7_m	insulin dependent diabetes susceptibility 7 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8401590
1300714	Idd7_m	insulin dependent diabetes susceptibility 7 (mouse)	qtl	MP:0005002	abnormal T cell clonal deletion		IAGP		N	RGD:5509061	20111116	MGI			PMID:18292549
1300714	Idd7_m	insulin dependent diabetes susceptibility 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8401590|PMID:18292549|PMID:7556956
1300714	Idd7_m	insulin dependent diabetes susceptibility 7 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8401590|PMID:18292549|PMID:7556956
1300714	Idd7_m	insulin dependent diabetes susceptibility 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8401590|PMID:18292549|PMID:7556956
1300714	Idd7_m	insulin dependent diabetes susceptibility 7 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8401590|PMID:18292549|PMID:7556956
1300716	Cd4ts4_m	CD4 T cell subset 4 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300716	Cd4ts4_m	CD4 T cell subset 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300716	Cd4ts4_m	CD4 T cell subset 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300720	Skl2_m	skeletal size (tail length) 2 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1300720	Skl2_m	skeletal size (tail length) 2 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1300721	Cfbw3_m	cystic fibrosis body weight 3 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12461646
1300721	Cfbw3_m	cystic fibrosis body weight 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12461646
1300722	Sle3_m	systemic lupus erythmatosus susceptibility 3 (mouse)	qtl	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9922399
1300722	Sle3_m	systemic lupus erythmatosus susceptibility 3 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9922399
1300722	Sle3_m	systemic lupus erythmatosus susceptibility 3 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9922399
1300722	Sle3_m	systemic lupus erythmatosus susceptibility 3 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10352264
1300722	Sle3_m	systemic lupus erythmatosus susceptibility 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10352264
1300722	Sle3_m	systemic lupus erythmatosus susceptibility 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10352264
1300722	Sle3_m	systemic lupus erythmatosus susceptibility 3 (mouse)	qtl	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:18607347
1300722	Sle3_m	systemic lupus erythmatosus susceptibility 3 (mouse)	qtl	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:18607347
1300724	Idd5a_m	insulin dependent diabetes susceptibility 5a (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11016460
1300724	Idd5a_m	insulin dependent diabetes susceptibility 5a (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210771
1300724	Idd5a_m	insulin dependent diabetes susceptibility 5a (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:18056379
1300724	Idd5a_m	insulin dependent diabetes susceptibility 5a (mouse)	qtl	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20260611	MGI			PMID:11723074
1300724	Idd5a_m	insulin dependent diabetes susceptibility 5a (mouse)	qtl	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20260611	MGI			PMID:11723074
1300726	Pitm4_m	prion incubation time 4 (mouse)	qtl	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11404459
1300726	Pitm4_m	prion incubation time 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11404459
1300727	Mptp1_m	MPTP sensitivity 1 (mouse)	qtl	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12591164
1300727	Mptp1_m	MPTP sensitivity 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12591164
1300729	Paam2_m	progression of autoimmune arthritis in MRL mice 2 (mouse)	qtl	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20111116	MGI			PMID:11953986
1300729	Paam2_m	progression of autoimmune arthritis in MRL mice 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11953986
1300731	Smdq3_m	segregation of mitochondrial DNA QTL 3 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12539044
1300731	Smdq3_m	segregation of mitochondrial DNA QTL 3 (mouse)	qtl	MP:0006037	abnormal mitochondrial fission		IAGP		N	RGD:5509061	20111116	MGI			PMID:12539044
1300732	Melm2_m	melanoma modifier 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11092979
1300732	Melm2_m	melanoma modifier 2 (mouse)	qtl	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20111116	MGI			PMID:11092979
1300732	Melm2_m	melanoma modifier 2 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11092979
1300732	Melm2_m	melanoma modifier 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11092979
1300734	Hdlq25_m	HDL QTL 25 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1300734	Hdlq25_m	HDL QTL 25 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1300740	Tne1_m	total number errors (mouse)	qtl	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529272
1300740	Tne1_m	total number errors (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529272
1300741	Idd17_m	insulin dependent diabetes susceptibility 17 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9257847
1300741	Idd17_m	insulin dependent diabetes susceptibility 17 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9257847
1300743	Skull6_m	skull morphology 6 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1300743	Skull6_m	skull morphology 6 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300743	Skull6_m	skull morphology 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300745	Gvhd1_m	graft-versus-host disease 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10233703
1300745	Gvhd1_m	graft-versus-host disease 1 (mouse)	qtl	MP:0005672	increased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20111116	MGI			PMID:10233703
1300746	Skl1_m	skeletal size (tail length) 1 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1300746	Skl1_m	skeletal size (tail length) 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1300747	Skts2_m	skin tumor susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7670492
1300747	Skts2_m	skin tumor susceptibility 2 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:7670492
1300747	Skts2_m	skin tumor susceptibility 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7670492
1300752	Ap6q_m	alcohol preference 6 QTL (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:11523702
1300752	Ap6q_m	alcohol preference 6 QTL (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:9726281
1300752	Ap6q_m	alcohol preference 6 QTL (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9726281
1300753	Eae10_m	susceptibility to experimental allergic encephalomyelitis 10 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9712054
1300753	Eae10_m	susceptibility to experimental allergic encephalomyelitis 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9712054
1300754	Lith4_m	lithogenic gene 4 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151694
1300754	Lith4_m	lithogenic gene 4 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151694
1300755	Wg3_m	weight gain in high growth mice 3 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1300755	Wg3_m	weight gain in high growth mice 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1300756	Pgia16_m	proteoglycan induced arthritis 16 (mouse)	qtl	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20111116	MGI			PMID:11046062
1300756	Pgia16_m	proteoglycan induced arthritis 16 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15084914|PMID:11046062
1300756	Pgia16_m	proteoglycan induced arthritis 16 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:11046062
1300757	Cocia9_m	cocaine induced activation 9 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1300757	Cocia9_m	cocaine induced activation 9 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1300757	Cocia9_m	cocaine induced activation 9 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1300758	Bomd4_m	bone mineral density 4 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11697792
1300758	Bomd4_m	bone mineral density 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11697792
1300759	Geot_m	geotaxia (mouse)	qtl	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1300759	Geot_m	geotaxia (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1300760	Nobq1_m	New Zealand obese QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18931681|PMID:11151768
1300760	Nobq1_m	New Zealand obese QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18931681|PMID:11151768
1300760	Nobq1_m	New Zealand obese QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18931681|PMID:11151768
1300766	Skull16_m	skull morphology 16 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1300766	Skull16_m	skull morphology 16 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300766	Skull16_m	skull morphology 16 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300767	Aliq4_m	acute lung injury QTL 4 (mouse)	qtl	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20111116	MGI			PMID:12718980
1300767	Aliq4_m	acute lung injury QTL 4 (mouse)	qtl	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20111116	MGI			PMID:11954676
1300767	Aliq4_m	acute lung injury QTL 4 (mouse)	qtl	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20111116	MGI			PMID:12718980
1300767	Aliq4_m	acute lung injury QTL 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11415940
1300769	Pcyts2_m	plasmacytoma susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12149518
1300769	Pcyts2_m	plasmacytoma susceptibility 2 (mouse)	qtl	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12149518
1300770	Ltsd6_m	lung tumor shape-determining 6 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517788
1300770	Ltsd6_m	lung tumor shape-determining 6 (mouse)	qtl	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517788
1300771	Fob2_m	F-line obesity QTL 2 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:10602985
1300771	Fob2_m	F-line obesity QTL 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10602985
1300773	Asbb2_m	autoimmune susceptibility in C57BL/6J and BALB/c 2 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:11994421
1300773	Asbb2_m	autoimmune susceptibility in C57BL/6J and BALB/c 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11994421
1300774	Pgia7_m	proteoglycan induced arthritis 7 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1300774	Pgia7_m	proteoglycan induced arthritis 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997|PMID:15084914
1300774	Pgia7_m	proteoglycan induced arthritis 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:10615997
1300775	Scpro1_m	stem cell proliferation 1 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10094931
1300775	Scpro1_m	stem cell proliferation 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10094931
1300775	Scpro1_m	stem cell proliferation 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10094931
1300776	Lfp3_m	long free running period 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309657
1300776	Lfp3_m	long free running period 3 (mouse)	qtl	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:11309657
1300777	Chol10_m	cholesterol 10 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14872007
1300777	Chol10_m	cholesterol 10 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14872007
1300778	Lprm4_m	lymphoproliferation modifier 4 (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:9403730
1300778	Lprm4_m	lymphoproliferation modifier 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9403730
1300778	Lprm4_m	lymphoproliferation modifier 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9403730
1300778	Lprm4_m	lymphoproliferation modifier 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9403730
1300779	Dyscalc4_m	dystrophic cardiac calcinosis 4 (mouse)	qtl	MP:0002838	decreased susceptibility to dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11526197
1300779	Dyscalc4_m	dystrophic cardiac calcinosis 4 (mouse)	qtl	MP:0002839	increased susceptibility to dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11526197
1300779	Dyscalc4_m	dystrophic cardiac calcinosis 4 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11526197
1300781	Lith8_m	lithogenic gene 8 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:12949731
1300781	Lith8_m	lithogenic gene 8 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12949731
1300782	Rear1_m	rearing 1 (mouse)	qtl	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14694905
1300782	Rear1_m	rearing 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14694905
1300784	Prdt3_m	prion disease incubation time 3 (mouse)	qtl	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12481985
1300784	Prdt3_m	prion disease incubation time 3 (mouse)	qtl	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12481985
1300784	Prdt3_m	prion disease incubation time 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11353827
1300786	Bw7_m	body weight QTL 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089|PMID:9725853
1300787	Cd8mts5_m	CD8 memory T cell subset 5 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300787	Cd8mts5_m	CD8 memory T cell subset 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300787	Cd8mts5_m	CD8 memory T cell subset 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300787	Cd8mts5_m	CD8 memory T cell subset 5 (mouse)	qtl	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300788	Cia2_m	collagen induced arthritis QTL 2 (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10051620
1300788	Cia2_m	collagen induced arthritis QTL 2 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:17082620
1300788	Cia2_m	collagen induced arthritis QTL 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11433381|PMID:10051620|PMID:15529344
1300788	Cia2_m	collagen induced arthritis QTL 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20140425	MGI		Created by mouse qtl pipeline	PMID:10051620
1300788	Cia2_m	collagen induced arthritis QTL 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11433381|PMID:10051620|PMID:15529344
1300788	Cia2_m	collagen induced arthritis QTL 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20140425	MGI		Created by mouse qtl pipeline	PMID:10051620
1300789	Idd18_m	insulin dependent diabetes susceptibility 18 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9530623
1300789	Idd18_m	insulin dependent diabetes susceptibility 18 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9530623
1300790	Pgia6_m	proteoglycan induced arthritis 6 (mouse)	qtl	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:12794840
1300790	Pgia6_m	proteoglycan induced arthritis 6 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12794840
1300790	Pgia6_m	proteoglycan induced arthritis 6 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1300790	Pgia6_m	proteoglycan induced arthritis 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997
1300790	Pgia6_m	proteoglycan induced arthritis 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997
1300791	Abbp3_m	A/J and C57BL/6 blood pressure 3 (mouse)	qtl	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20111116	MGI			PMID:14612590
1300791	Abbp3_m	A/J and C57BL/6 blood pressure 3 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14612590
1300792	Ltsd8_m	lung tumor shape-determining 8 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517788
1300792	Ltsd8_m	lung tumor shape-determining 8 (mouse)	qtl	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517788
1300794	Spha2_m	sperm head anomaly 2 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15020476
1300794	Spha2_m	sperm head anomaly 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15020476
1300794	Spha2_m	sperm head anomaly 2 (mouse)	qtl	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15020476
1300795	Stia2_m	serum transfer induced arthritis 2 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11489951
1300795	Stia2_m	serum transfer induced arthritis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11489951
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:11196712
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1300796	Lmr5_m	leishmaniasis resistance 5 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1300797	Sluc22_m	susceptibility to lung cancer 22 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1300797	Sluc22_m	susceptibility to lung cancer 22 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300799	Cfld2_m	cystic fibrosis lung disease 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:12461645
1300799	Cfld2_m	cystic fibrosis lung disease 2 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12461645
1300799	Cfld2_m	cystic fibrosis lung disease 2 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12461645
1300800	Ses3_m	salmonella enteritidis susceptibility 3 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058254
1300800	Ses3_m	salmonella enteritidis susceptibility 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058254|PMID:15973461
1300800	Ses3_m	salmonella enteritidis susceptibility 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20131011	MGI		Created by mouse qtl pipeline	PMID:15973461|PMID:12058254
1300800	Ses3_m	salmonella enteritidis susceptibility 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	PMID:12058254
1300804	Bw15_m	body weight QTL 15 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1300804	Bw15_m	body weight QTL 15 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1300806	Aod4_m	autoimmune ovarian dysgenesis 4 (mouse)	qtl	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20111116	MGI			PMID:12133995
1300806	Aod4_m	autoimmune ovarian dysgenesis 4 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12133995
1300806	Aod4_m	autoimmune ovarian dysgenesis 4 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12133995
1300807	Nidd1k_m	Nidd1 on KK-A<y> (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12115031
1300807	Nidd1k_m	Nidd1 on KK-A<y> (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12115031
1300808	Afw3_m	abdominal fat weight QTL 3 (mouse)	qtl	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:9725853
1300808	Afw3_m	abdominal fat weight QTL 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089|PMID:9725853
1300808	Afw3_m	abdominal fat weight QTL 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20141017	MGI		Created by mouse qtl pipeline	PMID:9725853
1300809	Ccrs2_m	corpus callosum hemisphere surface size 2 (mouse)	qtl	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:9804947
1300809	Ccrs2_m	corpus callosum hemisphere surface size 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9804947
1300811	Obq3_m	obesity QTL 3 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:9268627
1300811	Obq3_m	obesity QTL 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9268627
1300812	Oriq1_m	ovulation rate QTL 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300814	Artles_m	arterial lesions (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11463718
1300814	Artles_m	arterial lesions (mouse)	qtl	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11463718
1300814	Artles_m	arterial lesions (mouse)	qtl	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11463718
1300814	Artles_m	arterial lesions (mouse)	qtl	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11463718
1300814	Artles_m	arterial lesions (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11463718
1300814	Artles_m	arterial lesions (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11463718
1300817	Orgwq6_m	organ weight QTL 6 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1300817	Orgwq6_m	organ weight QTL 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12118102
1300817	Orgwq6_m	organ weight QTL 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1300817	Orgwq6_m	organ weight QTL 6 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1300818	Bbaa10_m	B.burgdorferi-associated arthritis 10 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1300818	Bbaa10_m	B.burgdorferi-associated arthritis 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1300819	Hpic3_m	haloperidol induced catalepsy 3 (mouse)	qtl	MP:0002822	catalepsy		IAGP		N	RGD:5509061	20111116	MGI			PMID:10454512
1300819	Hpic3_m	haloperidol induced catalepsy 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11166067
1300819	Hpic3_m	haloperidol induced catalepsy 3 (mouse)	qtl	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20111116	MGI			PMID:10454512
1300821	Lore1_m	loss of righting induced by ethanol 1 (mouse)	qtl	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1300821	Lore1_m	loss of righting induced by ethanol 1 (mouse)	qtl	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:8974320
1300821	Lore1_m	loss of righting induced by ethanol 1 (mouse)	qtl	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1300821	Lore1_m	loss of righting induced by ethanol 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8974320
1300821	Lore1_m	loss of righting induced by ethanol 1 (mouse)	qtl	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15365296
1300821	Lore1_m	loss of righting induced by ethanol 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8974320
1300821	Lore1_m	loss of righting induced by ethanol 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8974320
1300821	Lore1_m	loss of righting induced by ethanol 1 (mouse)	qtl	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1300822	Esmr_m	experimental severe malaria resistance (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11796577
1300822	Esmr_m	experimental severe malaria resistance (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11796577
1300823	Ath9_m	atherosclerosis 9 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11973313
1300823	Ath9_m	atherosclerosis 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973313
1300825	Wg1_m	weight gain in high growth mice 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1300825	Wg1_m	weight gain in high growth mice 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1300827	Cora1_m	correlation in cytokine production 1 (mouse)	qtl	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:9887350
1300827	Cora1_m	correlation in cytokine production 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9887350
1300828	Aod3_m	autoimmune ovarian dysgenesis 3 (mouse)	qtl	MP:0001868	ovary inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12133995
1300828	Aod3_m	autoimmune ovarian dysgenesis 3 (mouse)	qtl	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20111116	MGI			PMID:12133995
1300828	Aod3_m	autoimmune ovarian dysgenesis 3 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12133995
1300828	Aod3_m	autoimmune ovarian dysgenesis 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12133995
1300828	Aod3_m	autoimmune ovarian dysgenesis 3 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12133995
1300830	Bgeq1_m	body growth early QTL 1 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:10689807
1300830	Bgeq1_m	body growth early QTL 1 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:8846907
1300830	Bgeq1_m	body growth early QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8846907
1300835	Mwq1_m	molecular weight of quadriceps QTL 1 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1300835	Mwq1_m	molecular weight of quadriceps QTL 1 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1300838	Orgwq3_m	organ weight QTL 3 (mouse)	qtl	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1300838	Orgwq3_m	organ weight QTL 3 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1300838	Orgwq3_m	organ weight QTL 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12118102
1300839	Dyscalc2_m	dystrophic cardiac calcinosis 2 (mouse)	qtl	MP:0002838	decreased susceptibility to dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11526197
1300839	Dyscalc2_m	dystrophic cardiac calcinosis 2 (mouse)	qtl	MP:0002839	increased susceptibility to dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11526197
1300839	Dyscalc2_m	dystrophic cardiac calcinosis 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11526197
1300840	Cdcs3_m	cytokine deficiency colitis susceptibility 3 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11707574
1300840	Cdcs3_m	cytokine deficiency colitis susceptibility 3 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1300840	Cdcs3_m	cytokine deficiency colitis susceptibility 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1300841	Ssial1_m	susceptibility to sialadenitis 1 (mouse)	qtl	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11937580
1300841	Ssial1_m	susceptibility to sialadenitis 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1300841	Ssial1_m	susceptibility to sialadenitis 1 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1300841	Ssial1_m	susceptibility to sialadenitis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1300841	Ssial1_m	susceptibility to sialadenitis 1 (mouse)	qtl	MP:0005580	periinsulitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:1896073
1300842	Sle9_m	systematic lupus erythematosus susceptibility 9 (mouse)	qtl	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10693874
1300842	Sle9_m	systematic lupus erythematosus susceptibility 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10693874
1300844	Emo2_m	emotionality 2 (mouse)	qtl	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:10556431
1300844	Emo2_m	emotionality 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10556431
1300845	Leg1_m	longevity extending gene 1 (mouse)	qtl	MP:0001661	extended life span		IAGP		N	RGD:5509061	20111116	MGI			PMID:11568309
1300845	Leg1_m	longevity extending gene 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11568309
1300847	Par1_m	pulmonary adenoma resistance 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160222	MGI		Created by mouse qtl pipeline	PMID:8630506
1300847	Par1_m	pulmonary adenoma resistance 1 (mouse)	qtl	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20160218	MGI			PMID:17363568
1300847	Par1_m	pulmonary adenoma resistance 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20160222	MGI		Created by mouse qtl pipeline	PMID:8630506
1300848	Skull13_m	skull morphology 13 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1300848	Skull13_m	skull morphology 13 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300848	Skull13_m	skull morphology 13 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300849	Sles4_m	systemic lupus erythmatosus suppressor 4 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1300849	Sles4_m	systemic lupus erythmatosus suppressor 4 (mouse)	qtl	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1300849	Sles4_m	systemic lupus erythmatosus suppressor 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10485648
1300850	Mwq4_m	molecular weight of quadriceps QTL 4 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1300850	Mwq4_m	molecular weight of quadriceps QTL 4 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1300851	Heal4_m	wound healing/regeneration 4 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:12682777
1300851	Heal4_m	wound healing/regeneration 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20111116	MGI			PMID:12654824
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:12654824
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12058253
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300852	Lmr14_m	leishmaniasis resistance 14 (mouse)	qtl	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300853	Aggr2_m	aggression 2 (mouse)	qtl	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20111116	MGI			PMID:11826145
1300853	Aggr2_m	aggression 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11826145
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11196712
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300854	Lmr3_m	leishmaniasis resistance 3 (mouse)	qtl	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1300856	Nobq2_m	New Zealand obese QTL 2 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11151768
1300856	Nobq2_m	New Zealand obese QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11151768
1300858	Tafat_m	tally ho associated mesenteric fat pad weight (mouse)	qtl	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11414755
1300858	Tafat_m	tally ho associated mesenteric fat pad weight (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11414755
1300859	Skull8_m	skull morphology 8 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1300859	Skull8_m	skull morphology 8 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300859	Skull8_m	skull morphology 8 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300861	Bfq1_m	body fat QTL 1 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9276742
1300861	Bfq1_m	body fat QTL 1 (mouse)	qtl	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9276742
1300861	Bfq1_m	body fat QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9276742
1300861	Bfq1_m	body fat QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9276742
1300861	Bfq1_m	body fat QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9276742
1300861	Bfq1_m	body fat QTL 1 (mouse)	qtl	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9276742
1300861	Bfq1_m	body fat QTL 1 (mouse)	qtl	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9276742
1300862	Cfbw5_m	cystic fibrosis body weight 5 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12461646
1300862	Cfbw5_m	cystic fibrosis body weight 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12461646
1300863	Ltsd4_m	lung tumor shape-determining 4 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517788
1300863	Ltsd4_m	lung tumor shape-determining 4 (mouse)	qtl	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517788
1300864	Eae25_m	susceptibility to experimental allergic encephalomyelitis 25 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10706738
1300864	Eae25_m	susceptibility to experimental allergic encephalomyelitis 25 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10706738
1300864	Eae25_m	susceptibility to experimental allergic encephalomyelitis 25 (mouse)	qtl	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10706738
1300864	Eae25_m	susceptibility to experimental allergic encephalomyelitis 25 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10706738
1300867	Lore2_m	loss of righting induced by ethanol 2 (mouse)	qtl	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1300867	Lore2_m	loss of righting induced by ethanol 2 (mouse)	qtl	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:9880661
1300867	Lore2_m	loss of righting induced by ethanol 2 (mouse)	qtl	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1300867	Lore2_m	loss of righting induced by ethanol 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880661
1300867	Lore2_m	loss of righting induced by ethanol 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880661
1300867	Lore2_m	loss of righting induced by ethanol 2 (mouse)	qtl	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1300868	Tlf_m	T lymphocyte fraction (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9754812
1300868	Tlf_m	T lymphocyte fraction (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9754812
1300868	Tlf_m	T lymphocyte fraction (mouse)	qtl	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9754812
1300869	Stheal5_m	soft tissue heal 5 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11731492
1300869	Stheal5_m	soft tissue heal 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11731492
1300870	Ath18_m	atherosclerosis 18 (mouse)	qtl	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1300870	Ath18_m	atherosclerosis 18 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:9616220
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0005144	abnormal circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20120209	MGI			PMID:9616220
1300871	Mob5_m	multigenic obesity 5 (mouse)	qtl	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20130517	MGI			PMID:16873689
1300872	Afpq2_m	abdominal fat percent QTL 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089|PMID:9725853
1300874	Gasa2_m	gastritis type A susceptibility locus 2 (mouse)	qtl	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10227980
1300874	Gasa2_m	gastritis type A susceptibility locus 2 (mouse)	qtl	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11862406
1300874	Gasa2_m	gastritis type A susceptibility locus 2 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10227980
1300874	Gasa2_m	gastritis type A susceptibility locus 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10227980
1300876	Tanidd2_m	tally ho associated non-insulin dependednt diabetes mellitus 2 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11414755
1300876	Tanidd2_m	tally ho associated non-insulin dependednt diabetes mellitus 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11414755
1300877	Adip8_m	adiposity 8 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1300877	Adip8_m	adiposity 8 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1300878	Skts1_m	skin tumor susceptibility 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309660|PMID:7670492
1300878	Skts1_m	skin tumor susceptibility 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20150703	MGI		Created by mouse qtl pipeline	PMID:7670492
1300878	Skts1_m	skin tumor susceptibility 1 (mouse)	qtl	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:7670492
1300878	Skts1_m	skin tumor susceptibility 1 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:7670492
1300878	Skts1_m	skin tumor susceptibility 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309660|PMID:7670492
1300878	Skts1_m	skin tumor susceptibility 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20150703	MGI		Created by mouse qtl pipeline	PMID:7670492
1300879	Sle1b_m	systematic lupus erythematosus susceptibility 1b (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11172029
1300879	Sle1b_m	systematic lupus erythematosus susceptibility 1b (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11172029
1300881	Sluc29_m	susceptibility to lung cancer 29 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1300881	Sluc29_m	susceptibility to lung cancer 29 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300882	Ath17_m	atherosclerosis 17 (mouse)	qtl	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1300882	Ath17_m	atherosclerosis 17 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847
1300883	Ath21_m	atherosclerosis 21 (mouse)	qtl	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1300883	Ath21_m	atherosclerosis 21 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847
1300885	Mbis4_m	Mycobacterium bovis-induced systemic lupus erythematosus 4 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10903779
1300885	Mbis4_m	Mycobacterium bovis-induced systemic lupus erythematosus 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10903779
1300887	Pabr1_m	plasma apolipoprotein B (human) regulator 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11352992
1300887	Pabr1_m	plasma apolipoprotein B (human) regulator 1 (mouse)	qtl	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11352992
1300888	Berr1_m	berghei resistance locus 1 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12114535
1300888	Berr1_m	berghei resistance locus 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12114535
1300889	Lith9_m	lithogenic gene 9 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:12949731
1300889	Lith9_m	lithogenic gene 9 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151694
1300889	Lith9_m	lithogenic gene 9 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151694|PMID:12949731
1300889	Lith9_m	lithogenic gene 9 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20150724	MGI		Created by mouse qtl pipeline	PMID:12949731
1300890	Bhr3_m	bronchial hyperresponsiveness 3 (mouse)	qtl	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20111116	MGI			PMID:7550342
1300890	Bhr3_m	bronchial hyperresponsiveness 3 (mouse)	qtl	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20111116	MGI			PMID:7550342
1300890	Bhr3_m	bronchial hyperresponsiveness 3 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7550342
1300891	Obq8_m	obesity QTL 8 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210195
1300891	Obq8_m	obesity QTL 8 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210195
1300892	Szs10_m	seizure susceptibility 10 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11472065
1300892	Szs10_m	seizure susceptibility 10 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1300892	Szs10_m	seizure susceptibility 10 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1300894	Capop_m	cyclophosphamide induced apoptosis (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11247636
1300894	Capop_m	cyclophosphamide induced apoptosis (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11247636
1300894	Capop_m	cyclophosphamide induced apoptosis (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:11247636
1300894	Capop_m	cyclophosphamide induced apoptosis (mouse)	qtl	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11247636
1300895	Hdl5_m	HDL level 5 (mouse)	qtl	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12925895
1300895	Hdl5_m	HDL level 5 (mouse)	qtl	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18048852
1300895	Hdl5_m	HDL level 5 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12925895
1300895	Hdl5_m	HDL level 5 (mouse)	qtl	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18048852
1300895	Hdl5_m	HDL level 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18048852|PMID:12925895
1300895	Hdl5_m	HDL level 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:12925895
1300897	Cocia12_m	cocaine induced activation 12 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1300897	Cocia12_m	cocaine induced activation 12 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1300897	Cocia12_m	cocaine induced activation 12 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1300898	Cfid_m	cystic fibrosis intestinal distress (mouse)	qtl	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12441405
1300898	Cfid_m	cystic fibrosis intestinal distress (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20111116	MGI			PMID:12441405
1300898	Cfid_m	cystic fibrosis intestinal distress (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12441405
1300898	Cfid_m	cystic fibrosis intestinal distress (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12441405
1300899	Chol6_m	cholesterol 6 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12588951
1300899	Chol6_m	cholesterol 6 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12588951
1300899	Chol6_m	cholesterol 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12588951
1300901	Skts10_m	skin tumor susceptibility 10 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1300901	Skts10_m	skin tumor susceptibility 10 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10611333
1300901	Skts10_m	skin tumor susceptibility 10 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1300902	Hdl3_m	high density lipoprotein (HDL) level 3 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11108726
1300902	Hdl3_m	high density lipoprotein (HDL) level 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11108726
1300904	Chab5_m	cholesterol absorption 5 (mouse)	qtl	MP:0002646	increased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20111116	MGI			PMID:11714849
1300904	Chab5_m	cholesterol absorption 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1300904	Chab5_m	cholesterol absorption 5 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1300905	Scc6_m	colon tumor susceptibility 6 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10485458
1300905	Scc6_m	colon tumor susceptibility 6 (mouse)	qtl	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485458
1300905	Scc6_m	colon tumor susceptibility 6 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10485458
1300906	Ap8q_m	alcohol preference 8 QTL (mouse)	qtl	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:12176933
1300906	Ap8q_m	alcohol preference 8 QTL (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:12176933
1300906	Ap8q_m	alcohol preference 8 QTL (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12176933
1300908	Insq4_m	insulin QTL 4 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1300908	Insq4_m	insulin QTL 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11109545
1300909	Ath13_m	atherosclerosis 13 (mouse)	qtl	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11973313
1300909	Ath13_m	atherosclerosis 13 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973313
1300911	Idd19_m	insulin dependent diabetes susceptibility 19 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11386752
1300911	Idd19_m	insulin dependent diabetes susceptibility 19 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9647636
1300911	Idd19_m	insulin dependent diabetes susceptibility 19 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11386752|PMID:9647636
1300913	Bwefm_m	body weight females and males day 10 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1300913	Bwefm_m	body weight females and males day 10 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1300915	Lmr12_m	leishmaniasis resistance 12 (mouse)	qtl	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300915	Lmr12_m	leishmaniasis resistance 12 (mouse)	qtl	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1300915	Lmr12_m	leishmaniasis resistance 12 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1300915	Lmr12_m	leishmaniasis resistance 12 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1300915	Lmr12_m	leishmaniasis resistance 12 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12058253
1300915	Lmr12_m	leishmaniasis resistance 12 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1300915	Lmr12_m	leishmaniasis resistance 12 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1300915	Lmr12_m	leishmaniasis resistance 12 (mouse)	qtl	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300915	Lmr12_m	leishmaniasis resistance 12 (mouse)	qtl	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300916	Mobe2_m	modifier of obesity 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:14693723
1300916	Mobe2_m	modifier of obesity 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14693723
1300917	Gasa1_m	gastritis type A susceptibility locus 1 (mouse)	qtl	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10227980
1300917	Gasa1_m	gastritis type A susceptibility locus 1 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10227980
1300917	Gasa1_m	gastritis type A susceptibility locus 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10227980
1300918	Stheal4_m	soft tissue heal 4 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11731492
1300918	Stheal4_m	soft tissue heal 4 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:16341671
1300918	Stheal4_m	soft tissue heal 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16341671|PMID:11731492
1300918	Stheal4_m	soft tissue heal 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:11731492
1300919	Nidd2_m	non-insulin-dependent diabetes mellitus 2 (mouse)	qtl	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9703330
1300919	Nidd2_m	non-insulin-dependent diabetes mellitus 2 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9703330
1300919	Nidd2_m	non-insulin-dependent diabetes mellitus 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9703330
1300920	Pitm3_m	prion incubation time 3 (mouse)	qtl	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11404459
1300920	Pitm3_m	prion incubation time 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11404459
1300921	Skl4_m	skeletal size (tail length) 4 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1300921	Skl4_m	skeletal size (tail length) 4 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1300922	Actd1_m	activity-distance traveled 1 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:11105390
1300922	Actd1_m	activity-distance traveled 1 (mouse)	qtl	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:11105390
1300922	Actd1_m	activity-distance traveled 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11105390
1300923	Bits4_m	bitterness sensitivity 4 (mouse)	qtl	MP:0004210	abnormal bitter taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:10609087
1300923	Bits4_m	bitterness sensitivity 4 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10609087
1300924	Ity2_m	immunity to S. typhimurium 2 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9479490
1300924	Ity2_m	immunity to S. typhimurium 2 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:17660555
1300924	Ity2_m	immunity to S. typhimurium 2 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9479490
1300924	Ity2_m	immunity to S. typhimurium 2 (mouse)	qtl	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:16688529
1300924	Ity2_m	immunity to S. typhimurium 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9479490
1300925	Lbm4_m	lean body mass 4 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1300925	Lbm4_m	lean body mass 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1300926	Hpi2_m	hepatic PMN infiltration 2 (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11053246
1300926	Hpi2_m	hepatic PMN infiltration 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11053246
1300929	Pcyts1_m	plasmacytoma susceptibility 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12149518
1300929	Pcyts1_m	plasmacytoma susceptibility 1 (mouse)	qtl	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12149518
1300932	Hdlq17_m	HDL QTL 17 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1300932	Hdlq17_m	HDL QTL 17 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14872007
1300932	Hdlq17_m	HDL QTL 17 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847|PMID:14872007
1300932	Hdlq17_m	HDL QTL 17 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:14592847
1300933	Cdcs9_m	cytokine deficiency colitis susceptibility 9 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12213197
1300933	Cdcs9_m	cytokine deficiency colitis susceptibility 9 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12213197
1300933	Cdcs9_m	cytokine deficiency colitis susceptibility 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12213197
1300934	Cfbw1_m	cystic fibrosis body weight 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12461646
1300934	Cfbw1_m	cystic fibrosis body weight 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12461646
1300936	Dloc2_m	duration of locomotor activity 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14694905
1300936	Dloc2_m	duration of locomotor activity 2 (mouse)	qtl	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:14694905
1300938	Bulb3_m	bulb size 3 (mouse)	qtl	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529276
1300938	Bulb3_m	bulb size 3 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529276
1300939	Hrtfm6_m	heart failure modifier 6 (mouse)	qtl	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20111116	MGI			PMID:14519689
1300939	Hrtfm6_m	heart failure modifier 6 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14519689
1300939	Hrtfm6_m	heart failure modifier 6 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14519689
1300940	Actd3_m	activity-distance traveled 3 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:11105390
1300940	Actd3_m	activity-distance traveled 3 (mouse)	qtl	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:11105390
1300940	Actd3_m	activity-distance traveled 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11105390
1300941	Skl6_m	skeletal size (tail length) 6 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1300941	Skl6_m	skeletal size (tail length) 6 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1300943	Skts9_m	skin tumor susceptibility 9 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1300943	Skts9_m	skin tumor susceptibility 9 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10611333
1300943	Skts9_m	skin tumor susceptibility 9 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1300945	Bglq7_m	body growth late QTL 7 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:8846907
1300945	Bglq7_m	body growth late QTL 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8846907
1300946	Sle1c_m	systematic lupus erythematosus susceptibility 1c (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:17372026
1300946	Sle1c_m	systematic lupus erythematosus susceptibility 1c (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:17372026
1300946	Sle1c_m	systematic lupus erythematosus susceptibility 1c (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11172029
1300946	Sle1c_m	systematic lupus erythematosus susceptibility 1c (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11172029|PMID:17372026
1300946	Sle1c_m	systematic lupus erythematosus susceptibility 1c (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11172029|PMID:17372026
1300946	Sle1c_m	systematic lupus erythematosus susceptibility 1c (mouse)	qtl	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:17372026
1300948	Fglu2_m	fasting glucose 2 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12439655
1300948	Fglu2_m	fasting glucose 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12439655
1300949	Lore5_m	loss of righting induced by ethanol 5 (mouse)	qtl	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1300949	Lore5_m	loss of righting induced by ethanol 5 (mouse)	qtl	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1300949	Lore5_m	loss of righting induced by ethanol 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11964553
1300951	Gbvq1_m	gallstone bladder volume QTL 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12837957
1300951	Gbvq1_m	gallstone bladder volume QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12837957
1300951	Gbvq1_m	gallstone bladder volume QTL 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12837957
1300951	Gbvq1_m	gallstone bladder volume QTL 1 (mouse)	qtl	MP:0020132	increased gallbladder volume		IAGP		N	RGD:5509061	20200116	MGI			PMID:12837957
1300952	Hcs1_m	hepatocarcinogenesis susceptibility 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8417808
1300952	Hcs1_m	hepatocarcinogenesis susceptibility 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:8417808
1300952	Hcs1_m	hepatocarcinogenesis susceptibility 1 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8417808
1300954	Fcsa1_m	femoral cross-sectional area 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1300954	Fcsa1_m	femoral cross-sectional area 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1300954	Fcsa1_m	femoral cross-sectional area 1 (mouse)	qtl	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12369778
1300955	Pcpila2_m	PCP induced locomotor activity 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8914121
1300955	Pcpila2_m	PCP induced locomotor activity 2 (mouse)	qtl	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:8914121
1300956	Sle15_m	systematic lupus erythematosus susceptibility 15 (mouse)	qtl	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15034079
1300956	Sle15_m	systematic lupus erythematosus susceptibility 15 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15034079
1300956	Sle15_m	systematic lupus erythematosus susceptibility 15 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15034079
1300956	Sle15_m	systematic lupus erythematosus susceptibility 15 (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15034079
1300956	Sle15_m	systematic lupus erythematosus susceptibility 15 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:15034079
1300957	Pbd1_m	peak bone density 1 (mouse)	qtl	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20111116	MGI			PMID:9922384
1300957	Pbd1_m	peak bone density 1 (mouse)	qtl	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20111116	MGI			PMID:17295603
1300957	Pbd1_m	peak bone density 1 (mouse)	qtl	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20111116	MGI			PMID:9922384
1300957	Pbd1_m	peak bone density 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9922384
1300959	Lxw2_m	lupus BXSB x NZW 2 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14662843
1300959	Lxw2_m	lupus BXSB x NZW 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14662843
1300959	Lxw2_m	lupus BXSB x NZW 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14662843
1300960	Hpic2_m	haloperidol induced catalepsy 2 (mouse)	qtl	MP:0002822	catalepsy		IAGP		N	RGD:5509061	20111116	MGI			PMID:10765558
1300960	Hpic2_m	haloperidol induced catalepsy 2 (mouse)	qtl	MP:0002822	catalepsy		IAGP		N	RGD:5509061	20111116	MGI			PMID:17696997
1300960	Hpic2_m	haloperidol induced catalepsy 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10765558
1300961	Bh4p_m	bar holding four paws (mouse)	qtl	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1300961	Bh4p_m	bar holding four paws (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1300962	Cd8mts4_m	CD8 memory T cell subset 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300962	Cd8mts4_m	CD8 memory T cell subset 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1300962	Cd8mts4_m	CD8 memory T cell subset 4 (mouse)	qtl	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1300963	Hrl_m	herpes resistance locus (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14557652
1300963	Hrl_m	herpes resistance locus (mouse)	qtl	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:14557652
1300964	Hdlq22_m	HDL QTL 22 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1300964	Hdlq22_m	HDL QTL 22 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1300966	Pabr2_m	plasma apolipoprotein B (human) regulator 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11352992
1300966	Pabr2_m	plasma apolipoprotein B (human) regulator 2 (mouse)	qtl	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11352992
1300968	Skts4_m	skin tumor susceptibility 4 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9667751
1300968	Skts4_m	skin tumor susceptibility 4 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9667751
1300968	Skts4_m	skin tumor susceptibility 4 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9667751
1300969	Sluc5_m	susceptibility to lung cancer 5 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9809979
1300969	Sluc5_m	susceptibility to lung cancer 5 (mouse)	qtl	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300969	Sluc5_m	susceptibility to lung cancer 5 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300969	Sluc5_m	susceptibility to lung cancer 5 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1300969	Sluc5_m	susceptibility to lung cancer 5 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9809979
1300970	Cdcs4_m	cytokine deficiency colitis susceptibility 4 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11707574
1300970	Cdcs4_m	cytokine deficiency colitis susceptibility 4 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1300970	Cdcs4_m	cytokine deficiency colitis susceptibility 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1300971	Pgia14_m	proteoglycan induced arthritis 14 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11046062
1300971	Pgia14_m	proteoglycan induced arthritis 14 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11046062
1300971	Pgia14_m	proteoglycan induced arthritis 14 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11046062
1300972	Cocia11_m	cocaine induced activation 11 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1300972	Cocia11_m	cocaine induced activation 11 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1300972	Cocia11_m	cocaine induced activation 11 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1300973	Abmm_m	antibody mediated myocarditis (mouse)	qtl	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9887344
1300973	Abmm_m	antibody mediated myocarditis (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9887344
1300973	Abmm_m	antibody mediated myocarditis (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9887344
1300974	Pgia9_m	proteoglycan induced arthritis 9 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1300974	Pgia9_m	proteoglycan induced arthritis 9 (mouse)	qtl	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:18606685
1300974	Pgia9_m	proteoglycan induced arthritis 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18606685|PMID:10615997|PMID:15084914
1300974	Pgia9_m	proteoglycan induced arthritis 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:18606685|PMID:10615997
1300974	Pgia9_m	proteoglycan induced arthritis 9 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18606685|PMID:10615997|PMID:15084914
1300974	Pgia9_m	proteoglycan induced arthritis 9 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:18606685|PMID:10615997
1300974	Pgia9_m	proteoglycan induced arthritis 9 (mouse)	qtl	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:18606685
1300974	Pgia9_m	proteoglycan induced arthritis 9 (mouse)	qtl	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:18606685
1300975	Fembrs3_m	femur breaking strength 3 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:11991724
1300975	Fembrs3_m	femur breaking strength 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11991724
1300976	Bmd19_m	bone mineral density 19 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12568393
1300976	Bmd19_m	bone mineral density 19 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:12568393
1300977	Mopkd1_m	modifier of polycystic kidney disease progression 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9329956
1300977	Mopkd1_m	modifier of polycystic kidney disease progression 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9329956
1300977	Mopkd1_m	modifier of polycystic kidney disease progression 1 (mouse)	qtl	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20111116	MGI			PMID:9329956
1300979	Sbmd3_m	spinal bone mineral density 3 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:10780854
1300979	Sbmd3_m	spinal bone mineral density 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10780854
1300982	Lmr11_m	leishmaniasis resistance 11 (mouse)	qtl	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1300982	Lmr11_m	leishmaniasis resistance 11 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1300982	Lmr11_m	leishmaniasis resistance 11 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1300982	Lmr11_m	leishmaniasis resistance 11 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:12058253
1300982	Lmr11_m	leishmaniasis resistance 11 (mouse)	qtl	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1300984	Start1_m	startle response 1 (mouse)	qtl	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1300984	Start1_m	startle response 1 (mouse)	qtl	MP:0005377	hearing/vestibular/ear phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1300984	Start1_m	startle response 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1300985	Bmd13_m	bone mineral density 13 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11450694
1300985	Bmd13_m	bone mineral density 13 (mouse)	qtl	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20111116	MGI			PMID:17371164
1300985	Bmd13_m	bone mineral density 13 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694|PMID:12568393
1300986	Hdlq2_m	HDL QTL 2 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12006675
1300986	Hdlq2_m	HDL QTL 2 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1300986	Hdlq2_m	HDL QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12006675
1300987	Skull23_m	skull morphology 23 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1300987	Skull23_m	skull morphology 23 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300987	Skull23_m	skull morphology 23 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1300989	Lrdg1_m	light induced retinal degeneration 1 (mouse)	qtl	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20111116	MGI			PMID:15112105
1300989	Lrdg1_m	light induced retinal degeneration 1 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15112105
1300990	Bits3_m	bitterness sensitivity 3 (mouse)	qtl	MP:0004210	abnormal bitter taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:10609087
1300990	Bits3_m	bitterness sensitivity 3 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10609087
1300991	Cpfd4_m	cerebellum pattern fissures (mouse)	qtl	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529272
1300991	Cpfd4_m	cerebellum pattern fissures (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529272
1300992	Cocia14_m	cocaine induced activation 14 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1300992	Cocia14_m	cocaine induced activation 14 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1300992	Cocia14_m	cocaine induced activation 14 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1300995	Fembrs4_m	femur breaking strength 4 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:11991724
1300995	Fembrs4_m	femur breaking strength 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11991724
1300996	Aorls2_m	aortic lesion size 2 (mouse)	qtl	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20111116	MGI			PMID:12925895
1300996	Aorls2_m	aortic lesion size 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12925895
1300997	Eae15_m	susceptibility to experimental allergic encephalomyelitis 15 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1300997	Eae15_m	susceptibility to experimental allergic encephalomyelitis 15 (mouse)	qtl	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:10934166
1300999	Carp1_m	carcass protein in high growth mice 1 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1300999	Carp1_m	carcass protein in high growth mice 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301000	Obq5_m	obesity QTL 5 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:10501964
1301000	Obq5_m	obesity QTL 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10501964
1301003	Lmblgq4_m	limb length QTL 4 (mouse)	qtl	MP:0002764	short tibia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301003	Lmblgq4_m	limb length QTL 4 (mouse)	qtl	MP:0003109	short femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301003	Lmblgq4_m	limb length QTL 4 (mouse)	qtl	MP:0004351	short humerus		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301003	Lmblgq4_m	limb length QTL 4 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301003	Lmblgq4_m	limb length QTL 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301004	Hdlq27_m	HDL QTL 27 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1301004	Hdlq27_m	HDL QTL 27 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1301005	Idd16_m	insulin dependent diabetes susceptibility 16 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12086944
1301005	Idd16_m	insulin dependent diabetes susceptibility 16 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14513297
1301005	Idd16_m	insulin dependent diabetes susceptibility 16 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561967
1301005	Idd16_m	insulin dependent diabetes susceptibility 16 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14513297|PMID:15561967
1301006	Hfib1_m	hepatic fibrogenesis 1 (mouse)	qtl	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12454860
1301006	Hfib1_m	hepatic fibrogenesis 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12454860
1301007	Pid2_m	prion incubation determinant 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11013074
1301007	Pid2_m	prion incubation determinant 2 (mouse)	qtl	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11013074
1301009	Pbwg7_m	postnatal body weight growth 7 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1301009	Pbwg7_m	postnatal body weight growth 7 (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15056934
1301009	Pbwg7_m	postnatal body weight growth 7 (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1301009	Pbwg7_m	postnatal body weight growth 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15056934
1301010	ahl2_m	age related hearing loss 2 (mouse)	qtl	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20111116	MGI			PMID:12408962
1301010	ahl2_m	age related hearing loss 2 (mouse)	qtl	MP:0005377	hearing/vestibular/ear phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12408962
1301012	Vispl_m	visual placing (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1301013	Capsq4_m	capsaicin sensitivity related QTL 4 (mouse)	qtl	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14499433
1301013	Capsq4_m	capsaicin sensitivity related QTL 4 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14499433
1301014	Dob7_m	dietary obesity 7 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:9321464
1301014	Dob7_m	dietary obesity 7 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9321464
1301014	Dob7_m	dietary obesity 7 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9321464
1301014	Dob7_m	dietary obesity 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9321464
1301015	Sysbp2_m	systolic blood pressure 2 (mouse)	qtl	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20111116	MGI			PMID:10523337
1301015	Sysbp2_m	systolic blood pressure 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10523337
1301016	Szs1_m	seizure susceptibility 1 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:10436030
1301016	Szs1_m	seizure susceptibility 1 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11472065
1301016	Szs1_m	seizure susceptibility 1 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15112102
1301016	Szs1_m	seizure susceptibility 1 (mouse)	qtl	MP:0002064	seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:9069121
1301016	Szs1_m	seizure susceptibility 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301016	Szs1_m	seizure susceptibility 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301019	Bmd6_m	bone mineral density 6 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11450694
1301019	Bmd6_m	bone mineral density 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1301022	Morph4_m	morphine antinociception 4 (mouse)	qtl	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20111116	MGI			PMID:11420618
1301022	Morph4_m	morphine antinociception 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420618
1301022	Morph4_m	morphine antinociception 4 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420618
1301023	Sluc24_m	susceptibility to lung cancer 24 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1301023	Sluc24_m	susceptibility to lung cancer 24 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301024	Tbrs2_m	tuberculosis resistance 2 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11197687
1301024	Tbrs2_m	tuberculosis resistance 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11197687
1301025	Lbw7_m	lupus NZB x NZW 7 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:7937857
1301025	Lbw7_m	lupus NZB x NZW 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1301027	Hdlq12_m	HDL QTL 12 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12588951
1301027	Hdlq12_m	HDL QTL 12 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12588951
1301030	Bw4_m	body weight QTL 4 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9725853
1301030	Bw4_m	body weight QTL 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9725853
1301031	Bdln3_m	body length 3 (mouse)	qtl	MP:0001257	increased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:12856282
1301031	Bdln3_m	body length 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856282
1301032	Tauph_m	tau phosphorylation (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12514215
1301032	Tauph_m	tau phosphorylation (mouse)	qtl	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20140213	MGI			PMID:12514215
1301033	Abbp2_m	A/J and C57BL/6 blood pressure 2 (mouse)	qtl	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20111116	MGI			PMID:14612590
1301033	Abbp2_m	A/J and C57BL/6 blood pressure 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14612590
1301034	Egrm2_m	early growth rate (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12242647
1301034	Egrm2_m	early growth rate (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12242647
1301036	Axtofd4_m	anxiety-open field defecation 4 (mouse)	qtl	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:14990867
1301036	Axtofd4_m	anxiety-open field defecation 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769|PMID:14990867
1301036	Axtofd4_m	anxiety-open field defecation 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:14990867
1301036	Axtofd4_m	anxiety-open field defecation 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160506	MGI		Created by mouse qtl pipeline	PMID:11454769
1301037	Cd4ts5_m	CD4 T cell subset 5 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301037	Cd4ts5_m	CD4 T cell subset 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301037	Cd4ts5_m	CD4 T cell subset 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301037	Cd4ts5_m	CD4 T cell subset 5 (mouse)	qtl	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301038	C10bw3_m	castaneus 10 week body weight 3 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11003694
1301038	C10bw3_m	castaneus 10 week body weight 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11003694
1301039	Cbm4_m	cerebellum weight 4 (mouse)	qtl	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11438585
1301039	Cbm4_m	cerebellum weight 4 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11438585
1301041	Prnr2_m	prion resistance 2 (mouse)	qtl	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:14704188
1301041	Prnr2_m	prion resistance 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14704188
1301042	Elmaz1_m	elevated maze behavior 1 (mouse)	qtl	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20111116	MGI			PMID:11420611
1301042	Elmaz1_m	elevated maze behavior 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420611
1301045	Sluc10_m	susceptibility to lung cancer 10 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9809979
1301045	Sluc10_m	susceptibility to lung cancer 10 (mouse)	qtl	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301045	Sluc10_m	susceptibility to lung cancer 10 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301045	Sluc10_m	susceptibility to lung cancer 10 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301045	Sluc10_m	susceptibility to lung cancer 10 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9809979
1301046	Par3_m	pulmonary adenoma resistance 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11195459
1301046	Par3_m	pulmonary adenoma resistance 3 (mouse)	qtl	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:11195459
1301046	Par3_m	pulmonary adenoma resistance 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11195459
1301047	Bglq9_m	body growth late QTL 9 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:8846907
1301047	Bglq9_m	body growth late QTL 9 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8846907
1301048	Actre2_m	activity response to ethanol 2 (mouse)	qtl	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529277
1301048	Actre2_m	activity response to ethanol 2 (mouse)	qtl	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20111116	MGI			PMID:17143586
1301048	Actre2_m	activity response to ethanol 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:17143586|PMID:11529277
1301048	Actre2_m	activity response to ethanol 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20151225	MGI		Created by mouse qtl pipeline	PMID:11529277
1301049	El4_m	epilepsy 4 (mouse)	qtl	MP:0002064	seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:17010098
1301049	El4_m	epilepsy 4 (mouse)	qtl	MP:0002064	seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:8747920
1301049	El4_m	epilepsy 4 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8747920
1301049	El4_m	epilepsy 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8747920
1301051	Eae9_m	susceptibility to experimental allergic encephalomyelitis 9 (mouse)	qtl	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9712054
1301051	Eae9_m	susceptibility to experimental allergic encephalomyelitis 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7561115|PMID:9712054
1301051	Eae9_m	susceptibility to experimental allergic encephalomyelitis 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160729	MGI		Created by mouse qtl pipeline	PMID:9712054
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12829632
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11160299
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11386752
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7556956
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11484085
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11386752|PMID:8401590|PMID:11484085|PMID:11160299|PMID:7556956
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11386752|PMID:8401590|PMID:11484085|PMID:11160299|PMID:7556956
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11386752|PMID:8401590|PMID:11484085|PMID:11160299|PMID:7556956
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11386752|PMID:8401590|PMID:11484085|PMID:11160299|PMID:7556956
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12829632
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:18641312
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:18641312
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:18641312
1301053	Idd6_m	insulin dependent diabetes susceptibility 6 (mouse)	qtl	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1301054	Pcpila3_m	PCP induced locomotor activity 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8914121
1301054	Pcpila3_m	PCP induced locomotor activity 3 (mouse)	qtl	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:8914121
1301056	Pas2_m	pulmonary adenoma susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12810665|PMID:7813906
1301056	Pas2_m	pulmonary adenoma susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160212	MGI		Created by mouse qtl pipeline	PMID:7813906|PMID:12810665
1301057	Nidd4_m	non-insulin-dependent diabetes mellitus 4 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:10331427
1301057	Nidd4_m	non-insulin-dependent diabetes mellitus 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331427
1301058	Musz2_m	muscle size 2 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185459
1301058	Musz2_m	muscle size 2 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185459
1301059	Hrtfm1_m	heart failure modifier 1 (mouse)	qtl	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11956126
1301059	Hrtfm1_m	heart failure modifier 1 (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20111116	MGI			PMID:11956126
1301059	Hrtfm1_m	heart failure modifier 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11956126
1301059	Hrtfm1_m	heart failure modifier 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11956126
1301061	Nidd5_m	non-insulin-dependent diabetes mellitus 5 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10331427
1301061	Nidd5_m	non-insulin-dependent diabetes mellitus 5 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16688528
1301061	Nidd5_m	non-insulin-dependent diabetes mellitus 5 (mouse)	qtl	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10331427
1301061	Nidd5_m	non-insulin-dependent diabetes mellitus 5 (mouse)	qtl	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10331427
1301061	Nidd5_m	non-insulin-dependent diabetes mellitus 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331427
1301061	Nidd5_m	non-insulin-dependent diabetes mellitus 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331427
1301061	Nidd5_m	non-insulin-dependent diabetes mellitus 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331427
1301061	Nidd5_m	non-insulin-dependent diabetes mellitus 5 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331427
1301061	Nidd5_m	non-insulin-dependent diabetes mellitus 5 (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:16688528
1301062	Pltpq4_m	phospholipid transfer protein activity QTL 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592843
1301062	Pltpq4_m	phospholipid transfer protein activity QTL 4 (mouse)	qtl	MP:0012781	increased phospholipid transfer protein activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:14592843
1301064	Bwq4_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11515095
1301064	Bwq4_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11515095
1301065	Morph3_m	morphine antinociception 3 (mouse)	qtl	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20111116	MGI			PMID:11420618
1301065	Morph3_m	morphine antinociception 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420618
1301065	Morph3_m	morphine antinociception 3 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420618
1301066	Otx2m2_m	orthodenticle homolog 2 (Drosophila) modifier 2 (mouse)	qtl	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:12183386
1301066	Otx2m2_m	orthodenticle homolog 2 (Drosophila) modifier 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:12183386
1301066	Otx2m2_m	orthodenticle homolog 2 (Drosophila) modifier 2 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12183386
1301066	Otx2m2_m	orthodenticle homolog 2 (Drosophila) modifier 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12183386
1301069	Bw10_m	body weight QTL 10 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9725853
1301069	Bw10_m	body weight QTL 10 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9725853
1301070	Cypr1_m	cytokine production 1 (mouse)	qtl	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:9887350
1301070	Cypr1_m	cytokine production 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9887350
1301072	Eae22_m	experimental allergic encephalomyelitis 22 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10934166
1301072	Eae22_m	experimental allergic encephalomyelitis 22 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1301072	Eae22_m	experimental allergic encephalomyelitis 22 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1301072	Eae22_m	experimental allergic encephalomyelitis 22 (mouse)	qtl	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:10934166
1301073	Orch5_m	autoimmune orchitis resistance 5 (mouse)	qtl	MP:0001875	testis inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:7777570
1301073	Orch5_m	autoimmune orchitis resistance 5 (mouse)	qtl	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:7777570
1301073	Orch5_m	autoimmune orchitis resistance 5 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20141219	MGI		Created by mouse qtl pipeline	PMID:7777570
1301073	Orch5_m	autoimmune orchitis resistance 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7777570
1301073	Orch5_m	autoimmune orchitis resistance 5 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7777570
1301074	Axtofa3_m	anxiety-open field activity 3 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14990867
1301074	Axtofa3_m	anxiety-open field activity 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769|PMID:14990867
1301074	Axtofa3_m	anxiety-open field activity 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:14990867
1301074	Axtofa3_m	anxiety-open field activity 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160506	MGI		Created by mouse qtl pipeline	PMID:11454769
1301075	Obq10_m	obesity QTL 10 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210195
1301075	Obq10_m	obesity QTL 10 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210195
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15850792
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9257847
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9530623
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8401590|PMID:9257847|PMID:15850792|PMID:7556956
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20180330	MGI		Created by mouse qtl pipeline	PMID:9257847|PMID:15850792|PMID:8401590|PMID:7556956
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8401590|PMID:9257847|PMID:15850792|PMID:7556956
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20180330	MGI		Created by mouse qtl pipeline	PMID:9257847|PMID:15850792|PMID:8401590|PMID:7556956
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:8401590|PMID:9257847|PMID:15850792|PMID:7556956
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20180330	MGI		Created by mouse qtl pipeline	PMID:9257847|PMID:15850792|PMID:8401590|PMID:7556956
1301076	Idd10_m	insulin dependent diabetes susceptibility 10 (mouse)	qtl	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1301077	Pcpila1_m	PCP induced locomotor activity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8914121
1301077	Pcpila1_m	PCP induced locomotor activity 1 (mouse)	qtl	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:8914121
1301078	Alcp2_m	alcohol preference locus 2 (mouse)	qtl	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20120301	MGI			PMID:8640219
1301078	Alcp2_m	alcohol preference locus 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8640219
1301080	Sluc9_m	susceptibility to lung cancer 9 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9809979
1301080	Sluc9_m	susceptibility to lung cancer 9 (mouse)	qtl	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301080	Sluc9_m	susceptibility to lung cancer 9 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301080	Sluc9_m	susceptibility to lung cancer 9 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301080	Sluc9_m	susceptibility to lung cancer 9 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9809979
1301081	Cfsw3_m	cystic fibrosis survival to weaning 3 (mouse)	qtl	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20111116	MGI			PMID:12441405
1301081	Cfsw3_m	cystic fibrosis survival to weaning 3 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12441405
1301082	Bbaa16_m	B.burgdorferi-associated arthritis 16 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301082	Bbaa16_m	B.burgdorferi-associated arthritis 16 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1301083	Bhr5_m	bronchial hyperresponsiveness 5 (mouse)	qtl	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20150402	MGI			PMID:8624254
1301083	Bhr5_m	bronchial hyperresponsiveness 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10600881|PMID:15657107
1301083	Bhr5_m	bronchial hyperresponsiveness 5 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10600881|PMID:15657107
1301083	Bhr5_m	bronchial hyperresponsiveness 5 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:8624254
1301084	Bpq5_m	blood pressure QTL 5 (mouse)	qtl	MP:0000231	hypertension		IAGP		N	RGD:5509061	20111116	MGI			PMID:11161799
1301084	Bpq5_m	blood pressure QTL 5 (mouse)	qtl	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20111116	MGI			PMID:11161799
1301084	Bpq5_m	blood pressure QTL 5 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11161799
1301085	Lrnx10_m	learning-contextual 10 (mouse)	qtl	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:9354800
1301085	Lrnx10_m	learning-contextual 10 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9354800
1301086	Lprm5_m	lymphoproliferation modifier 5 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:9403730
1301086	Lprm5_m	lymphoproliferation modifier 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9403730
1301087	Bbaa15_m	B.burgdorferi-associated arthritis 15 (mouse)	qtl	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301087	Bbaa15_m	B.burgdorferi-associated arthritis 15 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1301087	Bbaa15_m	B.burgdorferi-associated arthritis 15 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:11704805
1301090	Eae23_m	experimental allergic encephalomyelitis 23 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10934166
1301090	Eae23_m	experimental allergic encephalomyelitis 23 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1301090	Eae23_m	experimental allergic encephalomyelitis 23 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1301090	Eae23_m	experimental allergic encephalomyelitis 23 (mouse)	qtl	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:10934166
1301091	Bbaa21_m	B.burgdorferi-associated arthritis 21 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301091	Bbaa21_m	B.burgdorferi-associated arthritis 21 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1301093	Igfbp3q2_m	insulin-like growth factor binding protein 3 QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11292658
1301093	Igfbp3q2_m	insulin-like growth factor binding protein 3 QTL 2 (mouse)	qtl	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11292658
1301095	El6_m	epilepsy 6 (mouse)	qtl	MP:0002064	seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:8747920
1301095	El6_m	epilepsy 6 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8747920
1301095	El6_m	epilepsy 6 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8747920
1301096	Obq1_m	obesity QTL 1 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:8786140
1301096	Obq1_m	obesity QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8786140
1301097	Bplpf1_m	bleomycin pulmonary fibrosis 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:9393751
1301097	Bplpf1_m	bleomycin pulmonary fibrosis 1 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9393751
1301097	Bplpf1_m	bleomycin pulmonary fibrosis 1 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9393751
1301098	Cd8mts3_m	CD8 memory T cell subset 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301098	Cd8mts3_m	CD8 memory T cell subset 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301098	Cd8mts3_m	CD8 memory T cell subset 3 (mouse)	qtl	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301099	Cbm2_m	cerebellum weight 2 (mouse)	qtl	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11438585
1301099	Cbm2_m	cerebellum weight 2 (mouse)	qtl	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11438585
1301099	Cbm2_m	cerebellum weight 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11438585
1301101	Hpnr4_m	Heligmosomoides polygyrus nematode resistance 4 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301103	Pgia11_m	proteoglycan induced arthritis 11 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1301103	Pgia11_m	proteoglycan induced arthritis 11 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997|PMID:15084914
1301103	Pgia11_m	proteoglycan induced arthritis 11 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:10615997
1301105	Cfld4_m	cystic fibrosis lung disease 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:12461645
1301105	Cfld4_m	cystic fibrosis lung disease 4 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12461645
1301105	Cfld4_m	cystic fibrosis lung disease 4 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12461645
1301106	Skts7_m	skin tumor susceptibility 7 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1301106	Skts7_m	skin tumor susceptibility 7 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10611333
1301106	Skts7_m	skin tumor susceptibility 7 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1301107	Scc4_m	colon tumor susceptibility 4 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8944029
1301107	Scc4_m	colon tumor susceptibility 4 (mouse)	qtl	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8944029
1301107	Scc4_m	colon tumor susceptibility 4 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:8944029
1301108	Scon2_m	sucrose consumption 2 (mouse)	qtl	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:9250857
1301108	Scon2_m	sucrose consumption 2 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9250857|PMID:10776660
1301108	Scon2_m	sucrose consumption 2 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:9250857
1301109	Dntcs2_m	dental caries susceptibility 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:14767162
1301109	Dntcs2_m	dental caries susceptibility 2 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14767162
1301109	Dntcs2_m	dental caries susceptibility 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20170929	MGI		Created by mouse qtl pipeline	PMID:14767162
1301109	Dntcs2_m	dental caries susceptibility 2 (mouse)	qtl	MP:0030101	carious teeth		IAGP		N	RGD:5509061	20170928	MGI			PMID:14767162
1301111	Mwq2_m	molecular weight of quadriceps QTL 2 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1301111	Mwq2_m	molecular weight of quadriceps QTL 2 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1301112	Szs9_m	seizure susceptibility 9 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11472065
1301112	Szs9_m	seizure susceptibility 9 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301112	Szs9_m	seizure susceptibility 9 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301114	Ssial2_m	susceptibility to sialadenitis 2 (mouse)	qtl	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11937580
1301114	Ssial2_m	susceptibility to sialadenitis 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1301114	Ssial2_m	susceptibility to sialadenitis 2 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1301114	Ssial2_m	susceptibility to sialadenitis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1301115	Lrdm1_m	lymphoproliferation (Fas) renal disease modifier 1 (mouse)	qtl	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:1460423
1301115	Lrdm1_m	lymphoproliferation (Fas) renal disease modifier 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9922399|PMID:1460423
1301115	Lrdm1_m	lymphoproliferation (Fas) renal disease modifier 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20150724	MGI		Created by mouse qtl pipeline	PMID:1460423
1301115	Lrdm1_m	lymphoproliferation (Fas) renal disease modifier 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9922399|PMID:1460423
1301115	Lrdm1_m	lymphoproliferation (Fas) renal disease modifier 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150724	MGI		Created by mouse qtl pipeline	PMID:1460423
1301116	Hdlq5_m	HDL QTL 5 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12805272
1301116	Hdlq5_m	HDL QTL 5 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12805272
1301116	Hdlq5_m	HDL QTL 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14872007|PMID:14701919|PMID:12805272
1301116	Hdlq5_m	HDL QTL 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:12805272
1301117	Fecq1_m	fecundity QTL 1 (mouse)	qtl	MP:0001934	increased litter size		IAGP		N	RGD:5509061	20111116	MGI			PMID:9457667
1301117	Fecq1_m	fecundity QTL 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9457667
1301118	Bbaa23_m	B.burgdorferi-associated arthritis 23 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301118	Bbaa23_m	B.burgdorferi-associated arthritis 23 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11431140
1301121	Obq13_m	obesity QTL 13 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210195
1301121	Obq13_m	obesity QTL 13 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210195
1301122	Cd8mts1_m	CD8 T memory cell subset 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301122	Cd8mts1_m	CD8 T memory cell subset 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301122	Cd8mts1_m	CD8 T memory cell subset 1 (mouse)	qtl	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301123	Cd8mts2_m	CD8 memory T cell subset 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301123	Cd8mts2_m	CD8 memory T cell subset 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301123	Cd8mts2_m	CD8 memory T cell subset 2 (mouse)	qtl	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301125	Sluc27_m	susceptibility to lung cancer 27 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1301125	Sluc27_m	susceptibility to lung cancer 27 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301126	Bwem1_m	body weight day 30 males 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1301126	Bwem1_m	body weight day 30 males 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1301127	Hpnr2_m	Heligmosomoides polygyrus nematode resistance 2 (mouse)	qtl	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301127	Hpnr2_m	Heligmosomoides polygyrus nematode resistance 2 (mouse)	qtl	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301127	Hpnr2_m	Heligmosomoides polygyrus nematode resistance 2 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12647241
1301127	Hpnr2_m	Heligmosomoides polygyrus nematode resistance 2 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783640
1301128	Sluc20_m	susceptibility to lung cancer 20 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1301128	Sluc20_m	susceptibility to lung cancer 20 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301128	Sluc20_m	susceptibility to lung cancer 20 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301130	Sle1a_m	systematic lupus erythematosus susceptibility 1a (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11172029
1301130	Sle1a_m	systematic lupus erythematosus susceptibility 1a (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11172029
1301132	Mors1_m	modifier of obesity related sterility 1 (mouse)	qtl	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20111116	MGI			PMID:9927300
1301132	Mors1_m	modifier of obesity related sterility 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9927300
1301133	Mob8_m	multigenic obesity 8 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:9616220
1301134	Bmd1_m	bone mineral density 1 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:10556421
1301134	Bmd1_m	bone mineral density 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10556421
1301135	Pas8_m	pulmonary adenoma susceptibility 8 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1301135	Pas8_m	pulmonary adenoma susceptibility 8 (mouse)	qtl	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301135	Pas8_m	pulmonary adenoma susceptibility 8 (mouse)	qtl	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301135	Pas8_m	pulmonary adenoma susceptibility 8 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1301135	Pas8_m	pulmonary adenoma susceptibility 8 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9790761
1301136	Pgia8_m	proteoglycan induced arthritis 8 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1301136	Pgia8_m	proteoglycan induced arthritis 8 (mouse)	qtl	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:18606685
1301136	Pgia8_m	proteoglycan induced arthritis 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18606685|PMID:10615997|PMID:15084914
1301136	Pgia8_m	proteoglycan induced arthritis 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:18606685|PMID:10615997
1301136	Pgia8_m	proteoglycan induced arthritis 8 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18606685|PMID:10615997|PMID:15084914
1301136	Pgia8_m	proteoglycan induced arthritis 8 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:18606685|PMID:10615997
1301136	Pgia8_m	proteoglycan induced arthritis 8 (mouse)	qtl	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:18606685
1301136	Pgia8_m	proteoglycan induced arthritis 8 (mouse)	qtl	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:18606685
1301137	Cocia8_m	cocaine induced activation 8 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1301137	Cocia8_m	cocaine induced activation 8 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301137	Cocia8_m	cocaine induced activation 8 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301138	Pcd4ts3_m	p-glycoprotein positive CD4 T cell subset 3 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301138	Pcd4ts3_m	p-glycoprotein positive CD4 T cell subset 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301138	Pcd4ts3_m	p-glycoprotein positive CD4 T cell subset 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301139	Lmr10_m	leishmaniasis resistance 10 (mouse)	qtl	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1301139	Lmr10_m	leishmaniasis resistance 10 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1301139	Lmr10_m	leishmaniasis resistance 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1301139	Lmr10_m	leishmaniasis resistance 10 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:12058253
1301140	Bbaa12_m	B.burgdorferi-associated arthritis 12 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301140	Bbaa12_m	B.burgdorferi-associated arthritis 12 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1301142	Heal2_m	wound healing/regeneration 2 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:9751744
1301142	Heal2_m	wound healing/regeneration 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777|PMID:9751744
1301142	Heal2_m	wound healing/regeneration 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:9751744
1301143	Skull17_m	skull morphology 17 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301143	Skull17_m	skull morphology 17 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301143	Skull17_m	skull morphology 17 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301145	Mob2_m	multigenic obesity 2 (mouse)	qtl	MP:0009290	increased femoral fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:7706460
1301146	Obq11_m	obesity QTL 11 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210195
1301146	Obq11_m	obesity QTL 11 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210195
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10744778
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0002139	abnormal hepatobiliary system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11682476
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0005085	abnormal gallbladder physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11682476
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10744778
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10744778|PMID:11682476
1301147	Diet1_m	variability in response to cholestrol enriched atherogenic diet (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10744778|PMID:11682476
1301150	Cara3_m	carcass ash in high growth mice 3 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1301150	Cara3_m	carcass ash in high growth mice 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301151	Hdlq14_m	HDL QTL 14 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1301151	Hdlq14_m	HDL QTL 14 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1301151	Hdlq14_m	HDL QTL 14 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847
1301152	Athsq2_m	atherosclerosis susceptibility QTL 2 (mouse)	qtl	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11438740
1301152	Athsq2_m	atherosclerosis susceptibility QTL 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11438740
1301153	Estq3_m	estradiol regulated response QTL 3 (mouse)	qtl	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9927277
1301153	Estq3_m	estradiol regulated response QTL 3 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9927277
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11016460
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:16172259
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10955330
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11016460
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15905556
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8661724
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:16172259
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:15905556|PMID:11016460|PMID:8401590|PMID:8384947
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20131011	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20220121	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590|PMID:26512207
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:15905556|PMID:11016460|PMID:8401590|PMID:8384947
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20131011	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20220121	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590|PMID:26512207
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:15905556|PMID:11016460|PMID:8401590|PMID:8384947
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20131011	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20220121	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590|PMID:26512207
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:15905556|PMID:11016460|PMID:8401590|PMID:8384947
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20131011	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20220121	MGI		Created by mouse qtl pipeline	PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590|PMID:26512207
1301154	Idd5_m	insulin dependent diabetes susceptibility 5 (mouse)	qtl	MP:0005580	periinsulitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8661724
1301155	Bpq7_m	blood pressure QTL 7 (mouse)	qtl	MP:0000231	hypertension		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118100
1301155	Bpq7_m	blood pressure QTL 7 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118100
1301156	Lbm1_m	lean body mass 1 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1301156	Lbm1_m	lean body mass 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1301157	Wt10q1_m	body weight (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1301157	Wt10q1_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1301158	Eae4_m	susceptibility to experimental allergic encephalomyelitis 4 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7561115
1301158	Eae4_m	susceptibility to experimental allergic encephalomyelitis 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7561115|PMID:10072563
1301158	Eae4_m	susceptibility to experimental allergic encephalomyelitis 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150717	MGI		Created by mouse qtl pipeline	PMID:7561115
1301159	Fob4_m	F-line obesity QTL 4 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:10602985
1301159	Fob4_m	F-line obesity QTL 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10602985
1301160	Eae14_m	susceptibility to experimental allergic encephalomyelitis 14 (mouse)	qtl	MP:0000921	demyelination		IAGP		N	RGD:5509061	20111116	MGI			PMID:10706738
1301160	Eae14_m	susceptibility to experimental allergic encephalomyelitis 14 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10706738
1301160	Eae14_m	susceptibility to experimental allergic encephalomyelitis 14 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10706738
1301160	Eae14_m	susceptibility to experimental allergic encephalomyelitis 14 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10706738
1301162	Skull1_m	skull morphology 1 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301162	Skull1_m	skull morphology 1 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301162	Skull1_m	skull morphology 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301163	Eae16_m	susceptibility to experimental allergic encephalomyelitis 16 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10934166
1301163	Eae16_m	susceptibility to experimental allergic encephalomyelitis 16 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1301163	Eae16_m	susceptibility to experimental allergic encephalomyelitis 16 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1301163	Eae16_m	susceptibility to experimental allergic encephalomyelitis 16 (mouse)	qtl	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:10934166
1301165	Lith7_m	lithogenic gene 7 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:12949731
1301165	Lith7_m	lithogenic gene 7 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12949731
1301166	Thypr2_m	thymocyte proliferative response 2 (mouse)	qtl	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12044964
1301166	Thypr2_m	thymocyte proliferative response 2 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12044964
1301166	Thypr2_m	thymocyte proliferative response 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12044964
1301166	Thypr2_m	thymocyte proliferative response 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12044964
1301167	Bgeq2_m	body growth early QTL 2 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:8846907
1301167	Bgeq2_m	body growth early QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10689807
1301170	Lith13_m	lithogenic gene 13 (mouse)	qtl	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12837957
1301170	Lith13_m	lithogenic gene 13 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12837957
1301172	Fembrs6_m	femur breaking strength 6 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:11991724
1301172	Fembrs6_m	femur breaking strength 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11991724
1301175	Ap7q_m	alcohol preference 7 QTL (mouse)	qtl	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:12176933
1301175	Ap7q_m	alcohol preference 7 QTL (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12176933
1301177	Vent3_m	ventricular size 3 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12746874
1301177	Vent3_m	ventricular size 3 (mouse)	qtl	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20140220	MGI			PMID:12746874
1301178	Lith10_m	lithogenic gene 10 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:12810825
1301178	Lith10_m	lithogenic gene 10 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12810825
1301179	Fembm4_m	femoral bone morphometry 4 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11518254
1301179	Fembm4_m	femoral bone morphometry 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11518254
1301179	Fembm4_m	femoral bone morphometry 4 (mouse)	qtl	MP:0030823	increased femur size		IAGP		N	RGD:5509061	20181018	MGI			PMID:11518254
1301181	Lbm6_m	lean body mass 6 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1301181	Lbm6_m	lean body mass 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1301183	Cadfar_m	cadmium-induced forelimb autopod reduction defect (mouse)	qtl	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10673332
1301183	Cadfar_m	cadmium-induced forelimb autopod reduction defect (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10673332
1301184	Bdln4_m	body length 4 (mouse)	qtl	MP:0001257	increased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:12856282
1301184	Bdln4_m	body length 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856282
1301185	Hdlq4_m	HDL QTL 4 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12006675
1301185	Hdlq4_m	HDL QTL 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12006675
1301186	Hlq2_m	heat loss QTL 2 (mouse)	qtl	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1301186	Hlq2_m	heat loss QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1301187	Adip9_m	adiposity 9 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:12856282
1301187	Adip9_m	adiposity 9 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856282
1301188	Heal6_m	wound healing/regeneration 6 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:9751744
1301188	Heal6_m	wound healing/regeneration 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777|PMID:9751744
1301188	Heal6_m	wound healing/regeneration 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:9751744
1301189	Lmr8_m	leishmaniasis resistance 8 (mouse)	qtl	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1301189	Lmr8_m	leishmaniasis resistance 8 (mouse)	qtl	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1301189	Lmr8_m	leishmaniasis resistance 8 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1301189	Lmr8_m	leishmaniasis resistance 8 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12058253
1301189	Lmr8_m	leishmaniasis resistance 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1301189	Lmr8_m	leishmaniasis resistance 8 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1301190	Cd4ts2_m	CD4 T cell subset 2 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301190	Cd4ts2_m	CD4 T cell subset 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301190	Cd4ts2_m	CD4 T cell subset 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301191	Stia1_m	serum transfer induced arthritis 1 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11489951
1301191	Stia1_m	serum transfer induced arthritis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11489951
1301192	Skts6_m	skin tumor susceptibility 6 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1301192	Skts6_m	skin tumor susceptibility 6 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10611333
1301192	Skts6_m	skin tumor susceptibility 6 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1301193	Lxw3_m	lupus BXSB x NZW 3 (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14662843
1301193	Lxw3_m	lupus BXSB x NZW 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14662843
1301196	Mnif1_m	macronutrient intake (mouse)	qtl	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:12388789
1301196	Mnif1_m	macronutrient intake (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12388789
1301197	Tlyr1_m	thymic lymphoma resistance 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12242666
1301197	Tlyr1_m	thymic lymphoma resistance 1 (mouse)	qtl	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12242666
1301198	Hdlq3_m	HDL QTL 3 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12006675
1301198	Hdlq3_m	HDL QTL 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12006675
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0001257	increased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:14981222
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:14981222
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:7706460
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14981222
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:7706460
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:14981222
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:14981222
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20111116	MGI			PMID:14981222
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:14981222
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:7706460
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:7706460
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20120209	MGI			PMID:14981222
1301200	Mob1_m	multigenic obesity 1 (mouse)	qtl	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20120209	MGI			PMID:7706460
1301201	Chab1_m	cholesterol absorption 1 (mouse)	qtl	MP:0002646	increased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20111116	MGI			PMID:11714849
1301201	Chab1_m	cholesterol absorption 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301201	Chab1_m	cholesterol absorption 1 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301202	Yaa4_m	Y-linked autoimmune acceleration 4 (mouse)	qtl	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9743333
1301202	Yaa4_m	Y-linked autoimmune acceleration 4 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9743333
1301202	Yaa4_m	Y-linked autoimmune acceleration 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9743333
1301204	Mob4_m	Multigenic obesity 4 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:7706460
1301205	Cms2_m	resistance to Coccidioides immitis 2 (mouse)	qtl	MP:0002409	decreased susceptibility to infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10338499
1301205	Cms2_m	resistance to Coccidioides immitis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10338499
1301206	Idd12_m	insulin dependent diabetes susceptibility 12 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8016086
1301206	Idd12_m	insulin dependent diabetes susceptibility 12 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8016086
1301207	Circp1_m	circadian photosensitivity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12465884
1301207	Circp1_m	circadian photosensitivity 1 (mouse)	qtl	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:12465884
1301210	Krcn_m	keratoconus (mouse)	qtl	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11773012
1301211	Bbaa11_m	B.burgdorferi-associated arthritis 11 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301211	Bbaa11_m	B.burgdorferi-associated arthritis 11 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1301212	Bw19_m	body weight QTL 19 (mouse)	qtl	MP:0001257	increased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:11535651
1301212	Bw19_m	body weight QTL 19 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:11535651
1301212	Bw19_m	body weight QTL 19 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:11535651
1301212	Bw19_m	body weight QTL 19 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449189
1301212	Bw19_m	body weight QTL 19 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449189
1301212	Bw19_m	body weight QTL 19 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449189
1301212	Bw19_m	body weight QTL 19 (mouse)	qtl	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20130328	MGI			PMID:11535651
1301215	Thcr_m	T helper cell response (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14568935
1301215	Thcr_m	T helper cell response (mouse)	qtl	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:14568935
1301215	Thcr_m	T helper cell response (mouse)	qtl	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:14568935
1301215	Thcr_m	T helper cell response (mouse)	qtl	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:14568935
1301215	Thcr_m	T helper cell response (mouse)	qtl	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:14568935
1301216	Cbm1_m	cerebellum weight 1 (mouse)	qtl	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11438585
1301216	Cbm1_m	cerebellum weight 1 (mouse)	qtl	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11438585
1301216	Cbm1_m	cerebellum weight 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11438585
1301220	Chol4_m	cholesterol 4 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10101257
1301220	Chol4_m	cholesterol 4 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16679719
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11956126
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20111116	MGI			PMID:16075368
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20111116	MGI			PMID:11956126
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20111116	MGI			PMID:16075368
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16075368|PMID:11956126
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:11956126
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16075368|PMID:11956126
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:11956126
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16075368|PMID:11956126
1301221	Hrtfm2_m	heart failure modifier 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:11956126
1301222	Scc7_m	colon tumor susceptibility 7 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10485458
1301222	Scc7_m	colon tumor susceptibility 7 (mouse)	qtl	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485458
1301222	Scc7_m	colon tumor susceptibility 7 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10485458
1301223	Hdlq7_m	HDL QTL 7 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12805272
1301223	Hdlq7_m	HDL QTL 7 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12805272
1301223	Hdlq7_m	HDL QTL 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12805272
1301224	Carfhg1_m	carcass fat in high growth mice 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301224	Carfhg1_m	carcass fat in high growth mice 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:11309659
1301224	Carfhg1_m	carcass fat in high growth mice 1 (mouse)	qtl	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1301225	Sle7_m	systematic lupus erythematosus susceptibility 7 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10693874
1301225	Sle7_m	systematic lupus erythematosus susceptibility 7 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10693874
1301225	Sle7_m	systematic lupus erythematosus susceptibility 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10693874
1301226	Bbaa2_m	B.burgdorferi-associated arthritis 2 (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:9916719
1301226	Bbaa2_m	B.burgdorferi-associated arthritis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9916719
1301227	Skull19_m	skull morphology 19 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301227	Skull19_m	skull morphology 19 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301227	Skull19_m	skull morphology 19 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301228	Iba4_m	induction of brown adipocytes 4 (mouse)	qtl	MP:0003012	obsolete no phenotypic analysis		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10931824
1301229	Bpq1_m	blood pressure QTL 1 (mouse)	qtl	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20111116	MGI			PMID:11161799
1301229	Bpq1_m	blood pressure QTL 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11161799
1301230	Idd5b_m	insulin dependent diabetes susceptibility 5b (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11016460
1301230	Idd5b_m	insulin dependent diabetes susceptibility 5b (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210771
1301230	Idd5b_m	insulin dependent diabetes susceptibility 5b (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:18056379
1301230	Idd5b_m	insulin dependent diabetes susceptibility 5b (mouse)	qtl	MP:0004031	insulitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:18056379
1301231	Chab6_m	cholesterol absorption 6 (mouse)	qtl	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20111116	MGI			PMID:11714849
1301231	Chab6_m	cholesterol absorption 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301231	Chab6_m	cholesterol absorption 6 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301232	Hcs7_m	hepatocarcinogenesis susceptibility 7 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15238534
1301232	Hcs7_m	hepatocarcinogenesis susceptibility 7 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	
1301232	Hcs7_m	hepatocarcinogenesis susceptibility 7 (mouse)	qtl	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20111116	MGI			PMID:15238534
1301232	Hcs7_m	hepatocarcinogenesis susceptibility 7 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	
1301232	Hcs7_m	hepatocarcinogenesis susceptibility 7 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:15238534
1301232	Hcs7_m	hepatocarcinogenesis susceptibility 7 (mouse)	qtl	MP:0010266	decreased liver tumor incidence		IEA		N	RGD:5509061	20111116	MGI			
1301233	Sbw2_m	splenomegaly-NZB x NZW 2 (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:7937857
1301233	Sbw2_m	splenomegaly-NZB x NZW 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:7937857
1301233	Sbw2_m	splenomegaly-NZB x NZW 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1301233	Sbw2_m	splenomegaly-NZB x NZW 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1301234	Hscfr_m	hematopoietic stem cell frequency regulator (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11777956
1301234	Hscfr_m	hematopoietic stem cell frequency regulator (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11777956
1301235	Alcw4_m	alcohol withdrawal 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8974318
1301235	Alcw4_m	alcohol withdrawal 4 (mouse)	qtl	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20111116	MGI			PMID:8974318
1301240	Sluc15_m	susceptibility to lung cancer 15 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1301240	Sluc15_m	susceptibility to lung cancer 15 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301241	Renf1_m	renal failure 1 (mouse)	qtl	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20111116	MGI			PMID:11839593
1301241	Renf1_m	renal failure 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11839593
1301242	Lbm5_m	lean body mass 5 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1301242	Lbm5_m	lean body mass 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1301243	Bmd2_m	bone mineral density 2 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:10556421
1301243	Bmd2_m	bone mineral density 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10556421
1301244	Ichs_m	immediate cutaneous hypersensitivity QTL (mouse)	qtl	MP:0002531	abnormal type I hypersensitivity reaction		IAGP		N	RGD:5509061	20111116	MGI			PMID:10941834
1301244	Ichs_m	immediate cutaneous hypersensitivity QTL (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10941834
1301247	Chol3_m	cholesterol 3 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10101257
1301248	Alaa1_m	alopecia areata (mouse)	qtl	MP:0000414	alopecia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12713579
1301248	Alaa1_m	alopecia areata (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12713579
1301249	Sbw1_m	splenomegaly-NZB x NZW 1 (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:7937857
1301249	Sbw1_m	splenomegaly-NZB x NZW 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:7937857
1301249	Sbw1_m	splenomegaly-NZB x NZW 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1301249	Sbw1_m	splenomegaly-NZB x NZW 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1301251	Scc3_m	colon tumor susceptibility 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8944029
1301251	Scc3_m	colon tumor susceptibility 3 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:14562056
1301252	Etohc3_m	ethanol consumption 3 (mouse)	qtl	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:7978106
1301252	Etohc3_m	ethanol consumption 3 (mouse)	qtl	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:9880656
1301252	Etohc3_m	ethanol consumption 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880656
1301253	Skmw2_m	skeletal muscle weight 2 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14679300
1301253	Skmw2_m	skeletal muscle weight 2 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14679300
1301253	Skmw2_m	skeletal muscle weight 2 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:14679300
1301253	Skmw2_m	skeletal muscle weight 2 (mouse)	qtl	MP:0009423	increased extensor digitorum longus weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1301254	Skts11_m	skin tumor susceptibility 11 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1301254	Skts11_m	skin tumor susceptibility 11 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10611333
1301254	Skts11_m	skin tumor susceptibility 11 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1301255	Cd4ts6_m	CD4 T cell subset 6 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301255	Cd4ts6_m	CD4 T cell subset 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301255	Cd4ts6_m	CD4 T cell subset 6 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301256	Skmw1_m	skeletal muscle weight 1 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14679300
1301256	Skmw1_m	skeletal muscle weight 1 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14679300
1301256	Skmw1_m	skeletal muscle weight 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:14679300
1301256	Skmw1_m	skeletal muscle weight 1 (mouse)	qtl	MP:0009421	increased gastrocnemius weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1301257	Yaa3_m	Y-linked autoimmune acceleration 3 (mouse)	qtl	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9743333
1301257	Yaa3_m	Y-linked autoimmune acceleration 3 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9743333
1301257	Yaa3_m	Y-linked autoimmune acceleration 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9743333
1301259	Hcs2_m	hepatocarcinogenesis susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8417808
1301259	Hcs2_m	hepatocarcinogenesis susceptibility 2 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:8417808
1301259	Hcs2_m	hepatocarcinogenesis susceptibility 2 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8417808
1301260	Exen1_m	exencephaly 1 (mouse)	qtl	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20111116	MGI			PMID:12856282
1301260	Exen1_m	exencephaly 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11598925
1301261	Hdl4_m	high density lipoprotein (HDL) level 4 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11108726
1301261	Hdl4_m	high density lipoprotein (HDL) level 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11108726
1301262	Gasa3_m	gastritis type A susceptibility locus 3 (mouse)	qtl	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11862406
1301262	Gasa3_m	gastritis type A susceptibility locus 3 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11862406
1301262	Gasa3_m	gastritis type A susceptibility locus 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11862406
1301263	Szs11_m	seizure susceptibility 11 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11472065
1301263	Szs11_m	seizure susceptibility 11 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:17698926
1301263	Szs11_m	seizure susceptibility 11 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301263	Szs11_m	seizure susceptibility 11 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301264	Cocia6_m	cocaine induced activation 6 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1301264	Cocia6_m	cocaine induced activation 6 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301264	Cocia6_m	cocaine induced activation 6 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301265	Idd21_m	insulin dependent diabetes susceptibility 21 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12856285
1301265	Idd21_m	insulin dependent diabetes susceptibility 21 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856285
1301266	Lmr4_m	leishmaniasis resistance 4 (mouse)	qtl	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1301266	Lmr4_m	leishmaniasis resistance 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1301266	Lmr4_m	leishmaniasis resistance 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1301266	Lmr4_m	leishmaniasis resistance 4 (mouse)	qtl	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1301266	Lmr4_m	leishmaniasis resistance 4 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1301267	Bcmd2_m	B cell maturation defect 2 (mouse)	qtl	MP:0000324	increased mast cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:11862404
1301267	Bcmd2_m	B cell maturation defect 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11862404
1301267	Bcmd2_m	B cell maturation defect 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11862404
1301268	Bmd14_m	bone mineral density 14 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1301268	Bmd14_m	bone mineral density 14 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1301268	Bmd14_m	bone mineral density 14 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1301269	Sluc12_m	susceptibility to lung cancer 12 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9809979
1301269	Sluc12_m	susceptibility to lung cancer 12 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301269	Sluc12_m	susceptibility to lung cancer 12 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301270	Dloc1_m	duration of locomotor activity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14694905
1301270	Dloc1_m	duration of locomotor activity 1 (mouse)	qtl	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:14694905
1301271	Datd_m	dopamine transporter density (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454925
1301271	Datd_m	dopamine transporter density (mouse)	qtl	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11454925
1301272	Cfsw1_m	cystic fibrosis survival to weaning 1 (mouse)	qtl	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20111116	MGI			PMID:12441405
1301272	Cfsw1_m	cystic fibrosis survival to weaning 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12441405
1301273	Wt6q1_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1301273	Wt6q1_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1301274	Lmr9_m	leishmaniasis resistance 9 (mouse)	qtl	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1301274	Lmr9_m	leishmaniasis resistance 9 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1301274	Lmr9_m	leishmaniasis resistance 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1301274	Lmr9_m	leishmaniasis resistance 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1301274	Lmr9_m	leishmaniasis resistance 9 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:12058253
1301274	Lmr9_m	leishmaniasis resistance 9 (mouse)	qtl	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1301275	Sle10_m	systematic lupus erythematosus susceptibility 10 (mouse)	qtl	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20111116	MGI			PMID:10693874
1301275	Sle10_m	systematic lupus erythematosus susceptibility 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10693874
1301276	Tswt_m	testis weight (mouse)	qtl	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15020476
1301276	Tswt_m	testis weight (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15020476
1301276	Tswt_m	testis weight (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15020476
1301277	nctm1_m	Nakano cataract modifier 1 (mouse)	qtl	MP:0001304	cataract		IAGP		N	RGD:5509061	20111116	MGI			PMID:12470976
1301277	nctm1_m	Nakano cataract modifier 1 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12470976
1301278	Bdln1_m	body length 1 (mouse)	qtl	MP:0001257	increased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:8833234
1301278	Bdln1_m	body length 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8833234
1301279	Obq4_m	obesity QTL 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9268627|PMID:11210195
1301279	Obq4_m	obesity QTL 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:9268627
1301279	Obq4_m	obesity QTL 4 (mouse)	qtl	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9268627
1301281	Frp2_m	free running period 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11381025
1301281	Frp2_m	free running period 2 (mouse)	qtl	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:11381025
1301282	Ses1_m	salmonella enteritidis susceptibility 1 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058254
1301282	Ses1_m	salmonella enteritidis susceptibility 1 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15973461
1301283	Alcw3_m	alcohol withdrawal 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12893462|PMID:16436183|PMID:12925894
1301283	Alcw3_m	alcohol withdrawal 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12893462|PMID:16436183|PMID:12925894
1301283	Alcw3_m	alcohol withdrawal 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:12893462
1301283	Alcw3_m	alcohol withdrawal 3 (mouse)	qtl	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20111116	MGI			PMID:12893462
1301283	Alcw3_m	alcohol withdrawal 3 (mouse)	qtl	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20111116	MGI			PMID:12893462
1301284	Cosz3_m	cocaine seizure 3 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:10734168
1301284	Cosz3_m	cocaine seizure 3 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10734168
1301284	Cosz3_m	cocaine seizure 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10734168
1301287	Feml2_m	femur length in high growth mice 2 (mouse)	qtl	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301287	Feml2_m	femur length in high growth mice 2 (mouse)	qtl	MP:0004348	long femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1301287	Feml2_m	femur length in high growth mice 2 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301287	Feml2_m	femur length in high growth mice 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301287	Feml2_m	femur length in high growth mice 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301288	Bw13_m	body weight QTL 13 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1301288	Bw13_m	body weight QTL 13 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1301289	Axtofa1_m	anxiety-open field activity 1 (mouse)	qtl	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14990867
1301289	Axtofa1_m	anxiety-open field activity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769|PMID:14990867
1301289	Axtofa1_m	anxiety-open field activity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11454769
1301290	Smgd1_m	submucosal gland distribution 1 (mouse)	qtl	MP:0002277	abnormal respiratory mucosa morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210181
1301290	Smgd1_m	submucosal gland distribution 1 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210181
1301292	Cfbw2_m	cystic fibrosis body weight 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12461646
1301292	Cfbw2_m	cystic fibrosis body weight 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12461646
1301293	Pgia13_m	proteoglycan induced arthritis 13 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11046062
1301293	Pgia13_m	proteoglycan induced arthritis 13 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15084914|PMID:11046062
1301293	Pgia13_m	proteoglycan induced arthritis 13 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:11046062
1301293	Pgia13_m	proteoglycan induced arthritis 13 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15084914|PMID:11046062
1301293	Pgia13_m	proteoglycan induced arthritis 13 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:11046062
1301294	Hrtfm5_m	heart failure modifier 5 (mouse)	qtl	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20111116	MGI			PMID:14519689
1301294	Hrtfm5_m	heart failure modifier 5 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14519689
1301294	Hrtfm5_m	heart failure modifier 5 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14519689
1301295	Prdt1_m	prion disease incubation time 1 (mouse)	qtl	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12481985
1301295	Prdt1_m	prion disease incubation time 1 (mouse)	qtl	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12481985
1301295	Prdt1_m	prion disease incubation time 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11353827
1301298	Pgia4_m	proteoglycan induced arthritis 4 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1301298	Pgia4_m	proteoglycan induced arthritis 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997|PMID:15084914
1301298	Pgia4_m	proteoglycan induced arthritis 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:10615997
1301299	Sluc23_m	susceptibility to lung cancer 23 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1301299	Sluc23_m	susceptibility to lung cancer 23 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301299	Sluc23_m	susceptibility to lung cancer 23 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301300	Lbm3_m	lean body mass 3 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1301300	Lbm3_m	lean body mass 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:16002707
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15986357
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15986357
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15986357
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:15986357
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:16002707
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:15986357
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8661718|PMID:16002707
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8661718|PMID:16002707
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8661718|PMID:16002707
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:15986357
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:18607347
1301301	Sle1_m	systemic lupus erythmatosus susceptibility 1 (mouse)	qtl	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:18607347
1301303	Alcp4_m	alcohol preference locus 4 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:10443995
1301303	Alcp4_m	alcohol preference locus 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880657
1301304	Hrq3_m	heart rate quantitative locus 3 (mouse)	qtl	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118100
1301304	Hrq3_m	heart rate quantitative locus 3 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118100
1301307	Phospq1_m	phospholipid QTL 1 (mouse)	qtl	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1301307	Phospq1_m	phospholipid QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11109545
1301308	Prdt4_m	prion disease incubation time 4 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11353827
1301308	Prdt4_m	prion disease incubation time 4 (mouse)	qtl	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11353827
1301309	Emo1_m	emotionality 1 (mouse)	qtl	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:10556431
1301309	Emo1_m	emotionality 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10556431
1301310	Tmevd5_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 5 (mouse)	qtl	MP:0000921	demyelination		IAGP		N	RGD:5509061	20111116	MGI			PMID:10482543
1301310	Tmevd5_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 5 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10482543
1301312	Hsm1_m	hereditary spherocytosis modifer 1 (mouse)	qtl	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20111116	MGI			PMID:15070709
1301312	Hsm1_m	hereditary spherocytosis modifer 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15070709
1301313	Pas5a_m	pulmonary adenoma susceptibility 5a (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11195459|PMID:8630506
1301313	Pas5a_m	pulmonary adenoma susceptibility 5a (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160219	MGI		Created by mouse qtl pipeline	PMID:11195459
1301313	Pas5a_m	pulmonary adenoma susceptibility 5a (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11195459|PMID:8630506
1301316	Dntcs1_m	dental caries susceptibility 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:14767162
1301316	Dntcs1_m	dental caries susceptibility 1 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14767162
1301316	Dntcs1_m	dental caries susceptibility 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20170929	MGI		Created by mouse qtl pipeline	PMID:14767162
1301316	Dntcs1_m	dental caries susceptibility 1 (mouse)	qtl	MP:0030101	carious teeth		IAGP		N	RGD:5509061	20170928	MGI			PMID:14767162
1301320	Ots1_m	ovarian teratoma susceptibility 1 (mouse)	qtl	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20111116	MGI			PMID:9044831
1301320	Ots1_m	ovarian teratoma susceptibility 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9044831
1301320	Ots1_m	ovarian teratoma susceptibility 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9044831
1301320	Ots1_m	ovarian teratoma susceptibility 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9044831
1301322	Lbm2_m	lean body mass 2 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1301322	Lbm2_m	lean body mass 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1301323	Asm2_m	autoimmune sialadenitis in MRL mice 2 (mouse)	qtl	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10616009
1301323	Asm2_m	autoimmune sialadenitis in MRL mice 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10616009
1301323	Asm2_m	autoimmune sialadenitis in MRL mice 2 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10616009
1301323	Asm2_m	autoimmune sialadenitis in MRL mice 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10616009
1301325	Pgia15_m	proteoglycan induced arthritis 15 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11046062
1301325	Pgia15_m	proteoglycan induced arthritis 15 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15084914|PMID:11046062
1301325	Pgia15_m	proteoglycan induced arthritis 15 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:11046062
1301325	Pgia15_m	proteoglycan induced arthritis 15 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15084914|PMID:11046062
1301325	Pgia15_m	proteoglycan induced arthritis 15 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20150925	MGI		Created by mouse qtl pipeline	PMID:11046062
1301327	Lmr7_m	leishmaniasis resistance 7 (mouse)	qtl	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11196712
1301327	Lmr7_m	leishmaniasis resistance 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11196712
1301327	Lmr7_m	leishmaniasis resistance 7 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1301327	Lmr7_m	leishmaniasis resistance 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1301327	Lmr7_m	leishmaniasis resistance 7 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11196712
1301327	Lmr7_m	leishmaniasis resistance 7 (mouse)	qtl	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1301332	Estq1_m	estradiol regulated response QTL 1 (mouse)	qtl	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:9927277
1301332	Estq1_m	estradiol regulated response QTL 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9176411
1301333	Mop3_m	morphine preference 3 (mouse)	qtl	MP:0002554	aversion to addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:8075641
1301333	Mop3_m	morphine preference 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8075641
1301334	Cocia10_m	cocaine induced activation 10 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1301334	Cocia10_m	cocaine induced activation 10 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301334	Cocia10_m	cocaine induced activation 10 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301335	Axtofa4_m	anxiety-open field activity 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769
1301337	Cdcs8_m	cytokine deficiency colitis susceptibility 8 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12213197
1301337	Cdcs8_m	cytokine deficiency colitis susceptibility 8 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12213197
1301337	Cdcs8_m	cytokine deficiency colitis susceptibility 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12213197
1301338	Lmr1_m	leishmaniasis resistance 1 (mouse)	qtl	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:16223880
1301338	Lmr1_m	leishmaniasis resistance 1 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:16223880
1301338	Lmr1_m	leishmaniasis resistance 1 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9151907
1301338	Lmr1_m	leishmaniasis resistance 1 (mouse)	qtl	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10508279
1301338	Lmr1_m	leishmaniasis resistance 1 (mouse)	qtl	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9151907
1301338	Lmr1_m	leishmaniasis resistance 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9151907
1301338	Lmr1_m	leishmaniasis resistance 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9151907
1301339	Hdlq15_m	HDL QTL 15 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1301339	Hdlq15_m	HDL QTL 15 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1301339	Hdlq15_m	HDL QTL 15 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18772481
1301339	Hdlq15_m	HDL QTL 15 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847|PMID:18048852
1301339	Hdlq15_m	HDL QTL 15 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:14592847
1301340	Bw16_m	body weight QTL 16 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1301340	Bw16_m	body weight QTL 16 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1301344	Lith1_m	lithogenic gene 1 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:11074014
1301344	Lith1_m	lithogenic gene 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11074014|PMID:12810825
1301344	Lith1_m	lithogenic gene 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20150717	MGI		Created by mouse qtl pipeline	PMID:11074014
1301346	Tmevd8_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 8 (mouse)	qtl	MP:0000921	demyelination		IAGP		N	RGD:5509061	20111116	MGI			PMID:12663542
1301346	Tmevd8_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 8 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12663542
1301347	Fpli_m	fasting plasma insulin (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12439655
1301347	Fpli_m	fasting plasma insulin (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12439655
1301349	Pgia26_m	proteoglycan induced arthritis 26 (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:12794840
1301349	Pgia26_m	proteoglycan induced arthritis 26 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:12794840
1301349	Pgia26_m	proteoglycan induced arthritis 26 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12794840
1301349	Pgia26_m	proteoglycan induced arthritis 26 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12794840
1301349	Pgia26_m	proteoglycan induced arthritis 26 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12794840
1301350	Nidd4k_m	Nidd4 on KK-A<y> (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12115031
1301350	Nidd4k_m	Nidd4 on KK-A<y> (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12115031
1301351	Obq6_m	obesity QTL 6 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10501964
1301351	Obq6_m	obesity QTL 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:10501964
1301351	Obq6_m	obesity QTL 6 (mouse)	qtl	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:10501964
1301352	Bis4_m	beta-carboline induced seizures 4 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:10234005
1301352	Bis4_m	beta-carboline induced seizures 4 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10234005
1301352	Bis4_m	beta-carboline induced seizures 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10234005
1301353	Lbw6_m	lupus NZB x NZW 6 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:7937857
1301353	Lbw6_m	lupus NZB x NZW 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1301354	Hcs4_m	hepatocarcinogenesis susceptibility 4 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7829059
1301354	Hcs4_m	hepatocarcinogenesis susceptibility 4 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:7829059
1301354	Hcs4_m	hepatocarcinogenesis susceptibility 4 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:7829059
1301355	Hipp2_m	hippocampal weight 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11331379
1301355	Hipp2_m	hippocampal weight 2 (mouse)	qtl	MP:0008282	enlarged hippocampus		IAGP		N	RGD:5509061	20111116	MGI			PMID:11331379
1301356	Idd8_m	insulin dependent diabetes susceptibility 8 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8401590
1301356	Idd8_m	insulin dependent diabetes susceptibility 8 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8401590
1301357	Hdlq32_m	HDL QTL 32 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1301357	Hdlq32_m	HDL QTL 32 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1301358	Eae20_m	experimental allergic encephalomyelitis 20 (mouse)	qtl	MP:0000921	demyelination		IAGP		N	RGD:5509061	20111116	MGI			PMID:10934166
1301358	Eae20_m	experimental allergic encephalomyelitis 20 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1301360	Stheal1_m	soft tissue heal 1 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11731492
1301360	Stheal1_m	soft tissue heal 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11731492
1301361	Idd14_m	insulin dependent diabetes susceptibility 14 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7556956
1301361	Idd14_m	insulin dependent diabetes susceptibility 14 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:17982459|PMID:7556956
1301362	Prnr1_m	prion resistance 1 (mouse)	qtl	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:14704188
1301362	Prnr1_m	prion resistance 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14704188
1301364	Lith14_m	lithogenic gene 14 (mouse)	qtl	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12837957
1301364	Lith14_m	lithogenic gene 14 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12837957|PMID:16151694
1301364	Lith14_m	lithogenic gene 14 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12837957|PMID:16151694
1301364	Lith14_m	lithogenic gene 14 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150724	MGI		Created by mouse qtl pipeline	PMID:12837957
1301365	Ap5q_m	alcohol preference 5 QTL (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:9726281
1301365	Ap5q_m	alcohol preference 5 QTL (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9726281
1301368	Par2_m	pulmonary adenoma resistance 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11195460|PMID:11494126|PMID:9331067
1301368	Par2_m	pulmonary adenoma resistance 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160729	MGI		Created by mouse qtl pipeline	PMID:11195460|PMID:11494126
1301368	Par2_m	pulmonary adenoma resistance 2 (mouse)	qtl	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11494126
1301368	Par2_m	pulmonary adenoma resistance 2 (mouse)	qtl	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955086
1301368	Par2_m	pulmonary adenoma resistance 2 (mouse)	qtl	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:8895504
1301368	Par2_m	pulmonary adenoma resistance 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11195460|PMID:11494126|PMID:9331067
1301368	Par2_m	pulmonary adenoma resistance 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20160729	MGI		Created by mouse qtl pipeline	PMID:11195460|PMID:11494126
1301368	Par2_m	pulmonary adenoma resistance 2 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11195460|PMID:11494126
1301369	Im4_m	immunoregulatory 4 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:8962125
1301369	Im4_m	immunoregulatory 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8962125
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301370	Adip1_m	adiposity 1 (mouse)	qtl	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:20388922
1301373	Vent2_m	ventricular size 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12746874
1301373	Vent2_m	ventricular size 2 (mouse)	qtl	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20140220	MGI			PMID:12746874
1301375	Tria4_m	T-cell receptor induced activation 4 (mouse)	qtl	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10384038
1301375	Tria4_m	T-cell receptor induced activation 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10384038
1301375	Tria4_m	T-cell receptor induced activation 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:10384038
1301376	Etohc1_m	ethanol consumption 1 (mouse)	qtl	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:9880656
1301376	Etohc1_m	ethanol consumption 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880656
1301377	Mprf_m	maternal performance (mouse)	qtl	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20111116	MGI			PMID:12454078
1301377	Mprf_m	maternal performance (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12454078
1301378	Hpdty_m	hindlimb polydactyly (mouse)	qtl	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20111116	MGI			PMID:15170224
1301378	Hpdty_m	hindlimb polydactyly (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15170224
1301379	Sials_m	sialoadenitis susceptibility (mouse)	qtl	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10980337
1301379	Sials_m	sialoadenitis susceptibility (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10980337
1301379	Sials_m	sialoadenitis susceptibility (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10980337
1301379	Sials_m	sialoadenitis susceptibility (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10980337
1301380	Cia8_m	collagen induced arthritis QTL 8 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10453039
1301380	Cia8_m	collagen induced arthritis QTL 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10453039|PMID:15761851
1301380	Cia8_m	collagen induced arthritis QTL 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:10453039
1301380	Cia8_m	collagen induced arthritis QTL 8 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10453039|PMID:15761851
1301381	Bomb1_m	bone marrow pre-B 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10363979
1301381	Bomb1_m	bone marrow pre-B 1 (mouse)	qtl	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:10363979
1301381	Bomb1_m	bone marrow pre-B 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10363979
1301381	Bomb1_m	bone marrow pre-B 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10363979
1301381	Bomb1_m	bone marrow pre-B 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10363979
1301381	Bomb1_m	bone marrow pre-B 1 (mouse)	qtl	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20131226	MGI			PMID:10363979
1301382	Arvm2_m	autoimmune renal vasculitis 2 (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10940892
1301382	Arvm2_m	autoimmune renal vasculitis 2 (mouse)	qtl	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10940892
1301382	Arvm2_m	autoimmune renal vasculitis 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10940892
1301382	Arvm2_m	autoimmune renal vasculitis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10940892
1301383	Aem2_m	anti-erythrocyte autoantibody modifier 2 (mouse)	qtl	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10607744
1301383	Aem2_m	anti-erythrocyte autoantibody modifier 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10607744
1301385	Radpf2_m	radiation pulmonary fibrosis 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:12097289
1301385	Radpf2_m	radiation pulmonary fibrosis 2 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12097289
1301385	Radpf2_m	radiation pulmonary fibrosis 2 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12097289
1301386	Sysbp1_m	systolic blood pressure 1 (mouse)	qtl	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20111116	MGI			PMID:10523337
1301386	Sysbp1_m	systolic blood pressure 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10523337
1301387	Chol8_m	cholesterol 8 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14701919
1301387	Chol8_m	cholesterol 8 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14701919
1301388	Hdlq21_m	HDL QTL 21 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1301388	Hdlq21_m	HDL QTL 21 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18772481|PMID:14993241
1301388	Hdlq21_m	HDL QTL 21 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:14993241
1301390	Hpnr6_m	Heligmosomoides polygyrus nematode resistance 6 (mouse)	qtl	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301392	Eae3_m	susceptibility to experimental allergic encephalomyelitis 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7545492|PMID:8757345
1301393	Dyscalc3_m	dystrophic cardiac calcinosis 3 (mouse)	qtl	MP:0002838	decreased susceptibility to dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11526197
1301393	Dyscalc3_m	dystrophic cardiac calcinosis 3 (mouse)	qtl	MP:0002839	increased susceptibility to dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11526197
1301393	Dyscalc3_m	dystrophic cardiac calcinosis 3 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11526197
1301394	Eae11_m	susceptibility to experimental allergic encephalomyelitis 11 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517969|PMID:10072563
1301394	Eae11_m	susceptibility to experimental allergic encephalomyelitis 11 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10072563
1301394	Eae11_m	susceptibility to experimental allergic encephalomyelitis 11 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517969|PMID:10072563
1301394	Eae11_m	susceptibility to experimental allergic encephalomyelitis 11 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150717	MGI		Created by mouse qtl pipeline	PMID:10072563
1301395	Wt10q3_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1301395	Wt10q3_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1301396	Apmt2_m	accelerator of polyoma-induced mammary tumors 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11003704
1301396	Apmt2_m	accelerator of polyoma-induced mammary tumors 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11003704
1301396	Apmt2_m	accelerator of polyoma-induced mammary tumors 2 (mouse)	qtl	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11003704
1301396	Apmt2_m	accelerator of polyoma-induced mammary tumors 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11003704
1301397	Amp2_m	amplitude of circadian rhythm 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11381025
1301397	Amp2_m	amplitude of circadian rhythm 2 (mouse)	qtl	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:11381025
1301398	Rapop3_m	radiation-induced apoptosis 3 (mouse)	qtl	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8825642
1301398	Rapop3_m	radiation-induced apoptosis 3 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8825642
1301399	Cpfd3_m	cerebellum pattern fissures (mouse)	qtl	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529272
1301399	Cpfd3_m	cerebellum pattern fissures (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529272
1301400	Lmr13_m	leishmaniasis resistance 13 (mouse)	qtl	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1301400	Lmr13_m	leishmaniasis resistance 13 (mouse)	qtl	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058253
1301400	Lmr13_m	leishmaniasis resistance 13 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1301400	Lmr13_m	leishmaniasis resistance 13 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1301400	Lmr13_m	leishmaniasis resistance 13 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:12058253
1301400	Lmr13_m	leishmaniasis resistance 13 (mouse)	qtl	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1301400	Lmr13_m	leishmaniasis resistance 13 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058253
1301401	Odsm1_m	ocular degeneration with sex reversal modifier 1 (mouse)	qtl	MP:0001939	secondary sex reversal		IAGP		N	RGD:5509061	20111116	MGI			PMID:12588798
1301401	Odsm1_m	ocular degeneration with sex reversal modifier 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12588798
1301402	Ap2q_m	alcohol preference 2 QTL (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:11523702
1301402	Ap2q_m	alcohol preference 2 QTL (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:9726281
1301402	Ap2q_m	alcohol preference 2 QTL (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9726281
1301404	Sbmd4_m	spinal bone mineral density 4 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:10780854
1301404	Sbmd4_m	spinal bone mineral density 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10780854
1301405	Etohr_m	ethanol response acute (mouse)	qtl	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20111116	MGI			PMID:9880575
1301405	Etohr_m	ethanol response acute (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880575
1301405	Etohr_m	ethanol response acute (mouse)	qtl	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20111116	MGI			PMID:9880575
1301407	Rapop2_m	radiation-induced apoptosis 2 (mouse)	qtl	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8825642
1301407	Rapop2_m	radiation-induced apoptosis 2 (mouse)	qtl	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9545495
1301407	Rapop2_m	radiation-induced apoptosis 2 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9545495|PMID:9367689
1301407	Rapop2_m	radiation-induced apoptosis 2 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:9545495
1301408	Lore8_m	loss of righting induced by ethanol 8 (mouse)	qtl	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11003198
1301408	Lore8_m	loss of righting induced by ethanol 8 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11003198
1301410	Cd8mts6_m	CD8 memory T cell subset 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301410	Cd8mts6_m	CD8 memory T cell subset 6 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301410	Cd8mts6_m	CD8 memory T cell subset 6 (mouse)	qtl	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301411	Pitm1_m	prion incubation time 1 (mouse)	qtl	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11404459
1301411	Pitm1_m	prion incubation time 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11404459
1301414	Heal10_m	wound healing/regeneration 10 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:12682777
1301414	Heal10_m	wound healing/regeneration 10 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777
1301417	Ltsd5_m	lung tumor shape-determining 5 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517788
1301417	Ltsd5_m	lung tumor shape-determining 5 (mouse)	qtl	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517788
1301419	Cypr3_m	cytokine production 3 (mouse)	qtl	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:9887350
1301419	Cypr3_m	cytokine production 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9887350
1301422	Sle11_m	systematic lupus erythematosus susceptibility 11 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10693874
1301422	Sle11_m	systematic lupus erythematosus susceptibility 11 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:10693874
1301422	Sle11_m	systematic lupus erythematosus susceptibility 11 (mouse)	qtl	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10693874
1301424	Skull21_m	skull morphology 21 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301424	Skull21_m	skull morphology 21 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301424	Skull21_m	skull morphology 21 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301426	Desp2_m	despair 2 (mouse)	qtl	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20111116	MGI			PMID:11875023
1301426	Desp2_m	despair 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11875023
1301430	Cdcs2_m	cytokine deficiency colitis susceptibility 2 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11707574
1301430	Cdcs2_m	cytokine deficiency colitis susceptibility 2 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1301430	Cdcs2_m	cytokine deficiency colitis susceptibility 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1301432	Hpnr1_m	Heligmosomoides polygyrus nematode resistance 1 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12647241
1301432	Hpnr1_m	Heligmosomoides polygyrus nematode resistance 1 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301432	Hpnr1_m	Heligmosomoides polygyrus nematode resistance 1 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783640
1301435	Trigq1_m	triglyceride QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18048852|PMID:14974682
1301435	Trigq1_m	triglyceride QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:14974682
1301436	Wg2_m	weight gain in high growth mice 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1301436	Wg2_m	weight gain in high growth mice 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301437	Scon1_m	sucrose consumption 1 (mouse)	qtl	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:9250857
1301437	Scon1_m	sucrose consumption 1 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9250857
1301438	Ltsd2_m	lung tumor shape-determining 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517788
1301438	Ltsd2_m	lung tumor shape-determining 2 (mouse)	qtl	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517788
1301439	Morph2_m	morphine antinociception 2 (mouse)	qtl	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20111116	MGI			PMID:11420618
1301439	Morph2_m	morphine antinociception 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420618
1301439	Morph2_m	morphine antinociception 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420618
1301441	Skull11_m	skull morphology 11 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301441	Skull11_m	skull morphology 11 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301441	Skull11_m	skull morphology 11 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301442	Pltpq1_m	phospholipid transfer protein activity QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592843
1301442	Pltpq1_m	phospholipid transfer protein activity QTL 1 (mouse)	qtl	MP:0012781	increased phospholipid transfer protein activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:14592843
1301443	Mopkd2_m	modifier of polycystic kidney disease progression 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9329956
1301443	Mopkd2_m	modifier of polycystic kidney disease progression 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9329956
1301443	Mopkd2_m	modifier of polycystic kidney disease progression 2 (mouse)	qtl	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20111116	MGI			PMID:9329956
1301445	Listr2_m	listeriosis resistance 2 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11242105
1301445	Listr2_m	listeriosis resistance 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11242105
1301446	Elsgp4_m	elevated serum gp70 4 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15067091
1301446	Elsgp4_m	elevated serum gp70 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15067091
1301447	Fembm3_m	femoral bone morphometry 3 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11518254
1301447	Fembm3_m	femoral bone morphometry 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11518254
1301447	Fembm3_m	femoral bone morphometry 3 (mouse)	qtl	MP:0030823	increased femur size		IAGP		N	RGD:5509061	20181018	MGI			PMID:11518254
1301449	Cia10_m	collagen induced arthritis 10 (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:9808201
1301449	Cia10_m	collagen induced arthritis 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9808201
1301450	Bpq6_m	blood pressure QTL 6 (mouse)	qtl	MP:0000231	hypertension		IAGP		N	RGD:5509061	20111116	MGI			PMID:11161799
1301450	Bpq6_m	blood pressure QTL 6 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11161799|PMID:12118100
1301450	Bpq6_m	blood pressure QTL 6 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11161799
1301451	Ath16_m	atherosclerosis 16 (mouse)	qtl	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11973313
1301451	Ath16_m	atherosclerosis 16 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973313
1301452	Elsgp1_m	elevated serum gp70 1 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10903778
1301452	Elsgp1_m	elevated serum gp70 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15067091|PMID:10903778
1301452	Elsgp1_m	elevated serum gp70 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150703	MGI		Created by mouse qtl pipeline	PMID:10903778
1301454	Eae5_m	susceptibility to experimental allergic encephalomyelitis 5 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9712054
1301454	Eae5_m	susceptibility to experimental allergic encephalomyelitis 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9712054
1301455	Bmd3_m	bone mineral density 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12568393|PMID:10556421
1301455	Bmd3_m	bone mineral density 3 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:12568393
1301456	Adip5_m	adiposity 5 (mouse)	qtl	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301456	Adip5_m	adiposity 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856282|PMID:11178736
1301456	Adip5_m	adiposity 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:11178736
1301456	Adip5_m	adiposity 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856282|PMID:11178736
1301457	Cfsw2_m	cystic fibrosis survival to weaning 2 (mouse)	qtl	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20111116	MGI			PMID:12441405
1301457	Cfsw2_m	cystic fibrosis survival to weaning 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12441405
1301458	Skts8_m	skin tumor susceptibility 8 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1301458	Skts8_m	skin tumor susceptibility 8 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10611333
1301458	Skts8_m	skin tumor susceptibility 8 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1301460	C10bw6_m	castaneus 10 week body weight 6 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11003694
1301460	C10bw6_m	castaneus 10 week body weight 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11003694
1301461	Chol9_m	cholesterol 9 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14701919
1301461	Chol9_m	cholesterol 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14701919
1301462	Nhdlq2_m	non-HDL QTL 2 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14701919
1301462	Nhdlq2_m	non-HDL QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14701919
1301463	Szs5_m	seizure susceptibility 5 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:10436030
1301463	Szs5_m	seizure susceptibility 5 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10436030
1301463	Szs5_m	seizure susceptibility 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10436030
1301466	T2dm2_m	type 2 diabetes mellitus 2 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11078464
1301466	T2dm2_m	type 2 diabetes mellitus 2 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11078464
1301466	T2dm2_m	type 2 diabetes mellitus 2 (mouse)	qtl	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16682971
1301466	T2dm2_m	type 2 diabetes mellitus 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11078464
1301468	Eye1_m	eye weight 1 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10102277
1301469	Cara2_m	carcass ash in high growth mice 2 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1301469	Cara2_m	carcass ash in high growth mice 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301470	Vmbic3_m	ventral midbrain iron content 3 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14744041
1301470	Vmbic3_m	ventral midbrain iron content 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14744041
1301470	Vmbic3_m	ventral midbrain iron content 3 (mouse)	qtl	MP:0020365	increased brain iron level		IAGP		N	RGD:5509061	20161020	MGI			PMID:14744041
1301471	Obq2_m	obesity QTL 2 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:8786140
1301471	Obq2_m	obesity QTL 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8786140
1301472	Pain1_m	pain 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11427320|PMID:15979798
1301472	Pain1_m	pain 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11427320|PMID:15979798
1301473	Triglq1_m	triglyceride QTL 1 (mouse)	qtl	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1301473	Triglq1_m	triglyceride QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11109545
1301475	Tnbs1_m	tri-nitrobenzene sulfonic acid susceptible 1 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301475	Tnbs1_m	tri-nitrobenzene sulfonic acid susceptible 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301475	Tnbs1_m	tri-nitrobenzene sulfonic acid susceptible 1 (mouse)	qtl	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12145808
1301477	Rencd_m	renal cystic disease severity (mouse)	qtl	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20111116	MGI			PMID:10864581
1301477	Rencd_m	renal cystic disease severity (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10864581
1301477	Rencd_m	renal cystic disease severity (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10864581
1301478	Eae26_m	susceptibility to experimental allergic encephalomyelitis 26 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11751755
1301478	Eae26_m	susceptibility to experimental allergic encephalomyelitis 26 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11751755
1301479	Sluc1_m	susceptibility to lung cancer 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160222	MGI		Created by mouse qtl pipeline	PMID:11584065
1301479	Sluc1_m	susceptibility to lung cancer 1 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20160225	MGI			PMID:11584065
1301480	Pbwg1_m	postnatal body weight growth 1 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11003694
1301480	Pbwg1_m	postnatal body weight growth 1 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1301480	Pbwg1_m	postnatal body weight growth 1 (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15056934
1301480	Pbwg1_m	postnatal body weight growth 1 (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1301480	Pbwg1_m	postnatal body weight growth 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11003694
1301481	Lith11_m	lithogenic gene 11 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:12810825
1301481	Lith11_m	lithogenic gene 11 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12810825
1301482	Morph1_m	morphine antinociception 1 (mouse)	qtl	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20111116	MGI			PMID:11420618
1301482	Morph1_m	morphine antinociception 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420618
1301482	Morph1_m	morphine antinociception 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420618
1301483	Obq12_m	obesity QTL 12 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210195
1301483	Obq12_m	obesity QTL 12 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210195
1301484	Bwq6_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12856282
1301484	Bwq6_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856282
1301485	Asthm1_m	asthma 1 (mouse)	qtl	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20111116	MGI			PMID:10072427
1301485	Asthm1_m	asthma 1 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10072427
1301487	Nociq1_m	nociceptive sensitivity inflammatory QTL 1 (mouse)	qtl	MP:0002735	abnormal chemical nociception		IAGP		N	RGD:5509061	20111116	MGI			PMID:11973013
1301487	Nociq1_m	nociceptive sensitivity inflammatory QTL 1 (mouse)	qtl	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11973013
1301487	Nociq1_m	nociceptive sensitivity inflammatory QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973013
1301487	Nociq1_m	nociceptive sensitivity inflammatory QTL 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973013
1301489	Lbm10_m	lean body mass 10 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1301489	Lbm10_m	lean body mass 10 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1301490	Pltpq2_m	phospholipid transfer protein activity QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592843
1301490	Pltpq2_m	phospholipid transfer protein activity QTL 2 (mouse)	qtl	MP:0012780	abnormal phospholipid transfer protein activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:14592843
1301491	Abbp4_m	A/J and C57BL/6 blood pressure 4 (mouse)	qtl	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20111116	MGI			PMID:14612590
1301491	Abbp4_m	A/J and C57BL/6 blood pressure 4 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14612590
1301492	Dbsty3_m	diabesity 3 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11042154
1301492	Dbsty3_m	diabesity 3 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11042154
1301492	Dbsty3_m	diabesity 3 (mouse)	qtl	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20111116	MGI			PMID:11042154
1301492	Dbsty3_m	diabesity 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11042154
1301492	Dbsty3_m	diabesity 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11042154
1301495	Cocia13_m	cocaine induced activation 13 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1301495	Cocia13_m	cocaine induced activation 13 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301495	Cocia13_m	cocaine induced activation 13 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301497	Tgls1_m	triglyceride level suppressor 1 (mouse)	qtl	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11473059
1301497	Tgls1_m	triglyceride level suppressor 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11473059
1301498	Oriq2_m	ovulation rate QTL 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301501	Lmr2_m	leishmaniasis resistance 2 (mouse)	qtl	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:16223880
1301501	Lmr2_m	leishmaniasis resistance 2 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:16223880
1301501	Lmr2_m	leishmaniasis resistance 2 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9151907
1301501	Lmr2_m	leishmaniasis resistance 2 (mouse)	qtl	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9151907
1301501	Lmr2_m	leishmaniasis resistance 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9151907
1301501	Lmr2_m	leishmaniasis resistance 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9151907
1301502	Eae17_m	susceptibility to experimental allergic encephalomyelitis 17 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10706738
1301502	Eae17_m	susceptibility to experimental allergic encephalomyelitis 17 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10706738
1301505	Tir1_m	trypanosome infection response 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9171834|PMID:12847546
1301505	Tir1_m	trypanosome infection response 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:9171834|PMID:12847546|PMID:8988870
1301505	Tir1_m	trypanosome infection response 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150626	MGI		Created by mouse qtl pipeline	PMID:9171834|PMID:8988870
1301506	Aevm1_m	autoimmune extremity vasculitis in MRL mice 1 (mouse)	qtl	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12746919
1301506	Aevm1_m	autoimmune extremity vasculitis in MRL mice 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12746919
1301506	Aevm1_m	autoimmune extremity vasculitis in MRL mice 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12746919
1301507	Actre1_m	activity response to ethanol 1 (mouse)	qtl	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20111116	MGI			PMID:12882366
1301507	Actre1_m	activity response to ethanol 1 (mouse)	qtl	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20111116	MGI			PMID:17143586
1301507	Actre1_m	activity response to ethanol 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12882366|PMID:11529277|PMID:17143586
1301507	Actre1_m	activity response to ethanol 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20151204	MGI		Created by mouse qtl pipeline	PMID:11529277|PMID:17143586
1301507	Actre1_m	activity response to ethanol 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20151225	MGI		Created by mouse qtl pipeline	PMID:11529277
1301508	Bulb4_m	bulb size 4 (mouse)	qtl	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529276
1301508	Bulb4_m	bulb size 4 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529276
1301510	Bbaa13_m	B.burgdorferi-associated arthritis 13 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301510	Bbaa13_m	B.burgdorferi-associated arthritis 13 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1301513	Idd9_m	insulin dependent diabetes susceptibility 9 (mouse)	qtl	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15905556
1301513	Idd9_m	insulin dependent diabetes susceptibility 9 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10933399
1301513	Idd9_m	insulin dependent diabetes susceptibility 9 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7556956
1301513	Idd9_m	insulin dependent diabetes susceptibility 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8199406|PMID:15905556|PMID:7556956
1301513	Idd9_m	insulin dependent diabetes susceptibility 9 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8199406|PMID:15905556|PMID:7556956
1301513	Idd9_m	insulin dependent diabetes susceptibility 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8199406|PMID:15905556|PMID:7556956
1301514	Rigs1_m	radiation induced gastroschisis 1 (mouse)	qtl	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20111116	MGI			PMID:9880666
1301514	Rigs1_m	radiation induced gastroschisis 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880666
1301515	Fembm1_m	femoral bone morphometry 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11518254
1301515	Fembm1_m	femoral bone morphometry 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11518254
1301515	Fembm1_m	femoral bone morphometry 1 (mouse)	qtl	MP:0030823	increased femur size		IAGP		N	RGD:5509061	20181018	MGI			PMID:11518254
1301516	Alan2_m	alloantigen response 2 (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11197689
1301516	Alan2_m	alloantigen response 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11197689
1301518	Bbaa5_m	B.burgdorferi-associated arthritis 5 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9916719
1301518	Bbaa5_m	B.burgdorferi-associated arthritis 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9916719
1301518	Bbaa5_m	B.burgdorferi-associated arthritis 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:9916719
1301519	Mbis1_m	Mycobacterium bovis-induced systemic lupus erythematosus 1 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10903779
1301519	Mbis1_m	Mycobacterium bovis-induced systemic lupus erythematosus 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10903779
1301521	Pas1c_m	pulmonary adenoma susceptibility 1c (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1301521	Pas1c_m	pulmonary adenoma susceptibility 1c (mouse)	qtl	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301521	Pas1c_m	pulmonary adenoma susceptibility 1c (mouse)	qtl	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301521	Pas1c_m	pulmonary adenoma susceptibility 1c (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1301521	Pas1c_m	pulmonary adenoma susceptibility 1c (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9790761
1301523	Ccrs1_m	corpus callosum hemisphere surface size 1 (mouse)	qtl	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:9804947
1301523	Ccrs1_m	corpus callosum hemisphere surface size 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9804947
1301524	Lmb2_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1301524	Lmb2_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1301524	Lmb2_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1301524	Lmb2_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:17548658
1301524	Lmb2_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9449705
1301524	Lmb2_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449705
1301524	Lmb2_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449705
1301524	Lmb2_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449705
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20111116	MGI			PMID:17548658
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:17548658
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:17548658
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9449705
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449705
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449705
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449705
1301525	Lmb1_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:17548658
1301527	Vmbic8_m	ventral midbrain iron content 8 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14744041
1301527	Vmbic8_m	ventral midbrain iron content 8 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14744041
1301527	Vmbic8_m	ventral midbrain iron content 8 (mouse)	qtl	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14744041
1301528	Loco1_m	locomotor activity 1 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:12226705
1301528	Loco1_m	locomotor activity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12226705
1301529	Nnc1_m	neuron number control 1 (mouse)	qtl	MP:0002983	increased retina ganglion cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9412494
1301529	Nnc1_m	neuron number control 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9412494
1301529	Nnc1_m	neuron number control 1 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9412494
1301530	Bglu2_m	blood glucose level 2 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:10894496
1301530	Bglu2_m	blood glucose level 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10894496
1301532	Scc8_m	colon tumor susceptibility 8 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10485458
1301532	Scc8_m	colon tumor susceptibility 8 (mouse)	qtl	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485458
1301532	Scc8_m	colon tumor susceptibility 8 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10485458
1301534	Idd20_m	insulin dependent diabetes susceptibility 20 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11386752
1301535	Pas5b_m	pulmonary adenoma susceptibility 5b (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1301535	Pas5b_m	pulmonary adenoma susceptibility 5b (mouse)	qtl	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301535	Pas5b_m	pulmonary adenoma susceptibility 5b (mouse)	qtl	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301535	Pas5b_m	pulmonary adenoma susceptibility 5b (mouse)	qtl	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301535	Pas5b_m	pulmonary adenoma susceptibility 5b (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1301535	Pas5b_m	pulmonary adenoma susceptibility 5b (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9790761
1301536	Pbbcp1_m	peripheral blood B cell percentage 1 (mouse)	qtl	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:11781239
1301536	Pbbcp1_m	peripheral blood B cell percentage 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11781239
1301536	Pbbcp1_m	peripheral blood B cell percentage 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11781239
1301539	Mwq5_m	molecular weight of quadriceps QTL 5 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1301539	Mwq5_m	molecular weight of quadriceps QTL 5 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1301540	Axtofa2_m	anxiety-open field activity 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769|PMID:14990867
1301542	Paam1_m	progression of autoimmune arthritis in MRL mice 1 (mouse)	qtl	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20111116	MGI			PMID:11953986
1301542	Paam1_m	progression of autoimmune arthritis in MRL mice 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11953986
1301543	Hypch_m	hypercholesterolemia (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12727230
1301543	Hypch_m	hypercholesterolemia (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12727230
1301544	Iba3_m	induction of brown adipocytes 3 (mouse)	qtl	MP:0003012	obsolete no phenotypic analysis		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10931824
1301545	Gauc_m	glucose area under curve (mouse)	qtl	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:12439655
1301545	Gauc_m	glucose area under curve (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12439655
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11756344
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15905556
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11756344
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15905556
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:1675432
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:7789623
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590
1301548	Idd4_m	insulin dependent diabetes susceptibility 4 (mouse)	qtl	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1301549	Bbaa9_m	B.burgdorferi-associated arthritis 9 (mouse)	qtl	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9916719
1301549	Bbaa9_m	B.burgdorferi-associated arthritis 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9916719
1301549	Bbaa9_m	B.burgdorferi-associated arthritis 9 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:9916719
1301550	Fembrs2_m	femur breaking strength 2 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:11991724
1301550	Fembrs2_m	femur breaking strength 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11991724
1301551	Spha1_m	sperm head anomaly 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15020476
1301551	Spha1_m	sperm head anomaly 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15020476
1301551	Spha1_m	sperm head anomaly 1 (mouse)	qtl	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15020476
1301554	Fatq1_m	percent fat (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1301554	Fatq1_m	percent fat (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1301556	Cd4vts1_m	CD4 virgin T cell subset 1 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301556	Cd4vts1_m	CD4 virgin T cell subset 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301556	Cd4vts1_m	CD4 virgin T cell subset 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301557	Bbaa22_m	B.burgdorferi-associated arthritis 22 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301557	Bbaa22_m	B.burgdorferi-associated arthritis 22 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1301558	Stheal8_m	soft tissue heal 8 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11731492
1301558	Stheal8_m	soft tissue heal 8 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:18028142
1301558	Stheal8_m	soft tissue heal 8 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11731492
1301559	Bbaa19_m	B.burgdorferi-associated arthritis 19 (mouse)	qtl	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301559	Bbaa19_m	B.burgdorferi-associated arthritis 19 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1301559	Bbaa19_m	B.burgdorferi-associated arthritis 19 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:11704805
1301560	Siafq1_m	stress induced analgesia (mouse)	qtl	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20111116	MGI			PMID:9315917
1301560	Siafq1_m	stress induced analgesia (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9315917
1301561	Chab2_m	cholesterol absorption 2 (mouse)	qtl	MP:0002646	increased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20111116	MGI			PMID:11714849
1301561	Chab2_m	cholesterol absorption 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301561	Chab2_m	cholesterol absorption 2 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301562	Hwq1_m	heart weight quantitative locus 1 (mouse)	qtl	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118100
1301562	Hwq1_m	heart weight quantitative locus 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12118100
1301562	Hwq1_m	heart weight quantitative locus 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118100
1301563	Alcp3_m	alcohol preference locus 3 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:9880657
1301563	Alcp3_m	alcohol preference locus 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880657
1301564	Pltpq3_m	phospholipid transfer protein activity QTL 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592843
1301564	Pltpq3_m	phospholipid transfer protein activity QTL 3 (mouse)	qtl	MP:0012781	increased phospholipid transfer protein activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:14592843
1301565	Mnotch_m	modifier of Notch (mouse)	qtl	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12388777
1301565	Mnotch_m	modifier of Notch (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12388777
1301566	Adip3_m	adiposity 3 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301566	Adip3_m	adiposity 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301569	Axtofd3_m	anxiety-open field defecation 3 (mouse)	qtl	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:14990867
1301569	Axtofd3_m	anxiety-open field defecation 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769|PMID:14990867
1301569	Axtofd3_m	anxiety-open field defecation 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11454769
1301571	Arrd1_m	age-related retinal degeneration 1 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12766041
1301571	Arrd1_m	age-related retinal degeneration 1 (mouse)	qtl	MP:0031605	decreased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:12766041
1301572	Sluc30_m	susceptibility to lung cancer 30 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1301572	Sluc30_m	susceptibility to lung cancer 30 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301574	Lmblgq5_m	limb length QTL 5 (mouse)	qtl	MP:0004348	long femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301574	Lmblgq5_m	limb length QTL 5 (mouse)	qtl	MP:0004357	long tibia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301574	Lmblgq5_m	limb length QTL 5 (mouse)	qtl	MP:0004370	long ulna		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301574	Lmblgq5_m	limb length QTL 5 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301574	Lmblgq5_m	limb length QTL 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301575	Tanidd3_m	tally ho associated non-insulin dependednt diabetes mellitus 3 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11414755
1301575	Tanidd3_m	tally ho associated non-insulin dependednt diabetes mellitus 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11414755
1301576	Wt6q2_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1301576	Wt6q2_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1301578	Feml3_m	femur length in high growth mice 3 (mouse)	qtl	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301578	Feml3_m	femur length in high growth mice 3 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301578	Feml3_m	femur length in high growth mice 3 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301578	Feml3_m	femur length in high growth mice 3 (mouse)	qtl	MP:0003109	short femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301578	Feml3_m	femur length in high growth mice 3 (mouse)	qtl	MP:0004348	long femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1301578	Feml3_m	femur length in high growth mice 3 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301578	Feml3_m	femur length in high growth mice 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301578	Feml3_m	femur length in high growth mice 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301580	Hrq2_m	heart rate quantitative locus 2 (mouse)	qtl	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118100
1301580	Hrq2_m	heart rate quantitative locus 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118100
1301581	Char2_m	P. chabaudi malaria resistance QTL 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9398835|PMID:15170228|PMID:9398834
1301584	Lrdg2_m	light induced retinal degeneration 2 (mouse)	qtl	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20111116	MGI			PMID:15112105
1301584	Lrdg2_m	light induced retinal degeneration 2 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15112105
1301585	Cd4ts1_m	CD4 T cell subset 1 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301585	Cd4ts1_m	CD4 T cell subset 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301585	Cd4ts1_m	CD4 T cell subset 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301586	Stheal3_m	soft tissue heal 3 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11731492
1301586	Stheal3_m	soft tissue heal 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11731492
1301587	Rrodp2_m	rotarod performance 2 (mouse)	qtl	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20111116	MGI			PMID:14694905
1301587	Rrodp2_m	rotarod performance 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14694905
1301588	Hrec_m	hemotopoietic response to early cytokines (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12010793
1301588	Hrec_m	hemotopoietic response to early cytokines (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12010793
1301589	Obq14_m	obesity QTL 14 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210195
1301589	Obq14_m	obesity QTL 14 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210195
1301590	Pbwg3_m	postnatal body weight growth 3 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1301590	Pbwg3_m	postnatal body weight growth 3 (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15056934
1301590	Pbwg3_m	postnatal body weight growth 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15056934
1301591	Chol7_m	cholesterol 7 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14701919
1301591	Chol7_m	cholesterol 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14701919
1301593	Heal8_m	wound healing/regeneration 8 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:9751744
1301593	Heal8_m	wound healing/regeneration 8 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777|PMID:9751744
1301593	Heal8_m	wound healing/regeneration 8 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:9751744
1301594	Aod1b_m	autoimmune ovarian dysgenesis 1b (mouse)	qtl	MP:0001868	ovary inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12794114
1301594	Aod1b_m	autoimmune ovarian dysgenesis 1b (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12794114
1301594	Aod1b_m	autoimmune ovarian dysgenesis 1b (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12794114
1301594	Aod1b_m	autoimmune ovarian dysgenesis 1b (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12794114
1301595	Wt3q1_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1301595	Wt3q1_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1301597	Anxty_m	anxiety (mouse)	qtl	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:12719372
1301597	Anxty_m	anxiety (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12719372
1301598	Renf2_m	renal failure 2 (mouse)	qtl	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20111116	MGI			PMID:11839593
1301598	Renf2_m	renal failure 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11839593
1301600	Hdlq29_m	HDL QTL 29 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1301600	Hdlq29_m	HDL QTL 29 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1301602	Bslm4_m	basal locomotor activity 4 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14722723
1301602	Bslm4_m	basal locomotor activity 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14722723
1301603	Hdl6_m	HDL level 6 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12925895
1301603	Hdl6_m	HDL level 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12925895
1301604	Eae1_m	susceptibility to experimental allergic encephalomyelitis 1 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:2579140
1301604	Eae1_m	susceptibility to experimental allergic encephalomyelitis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:2579140
1301606	Hdlq6_m	HDL QTL 6 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12805272
1301606	Hdlq6_m	HDL QTL 6 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12805272
1301606	Hdlq6_m	HDL QTL 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12805272
1301608	Emo3_m	emotionality 3 (mouse)	qtl	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:10080185
1301608	Emo3_m	emotionality 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10080185
1301612	Skmw4_m	skeletal muscle weight 4 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14679300
1301612	Skmw4_m	skeletal muscle weight 4 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14679300
1301614	Cgnz1_m	chronic glomerulonephritis in NZM 1 (mouse)	qtl	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11513551
1301614	Cgnz1_m	chronic glomerulonephritis in NZM 1 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:11513551
1301614	Cgnz1_m	chronic glomerulonephritis in NZM 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11513551
1301614	Cgnz1_m	chronic glomerulonephritis in NZM 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11513551
1301615	Cfld3_m	cystic fibrosis lung disease 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:12461645
1301615	Cfld3_m	cystic fibrosis lung disease 3 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12461645
1301615	Cfld3_m	cystic fibrosis lung disease 3 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12461645
1301616	Yaa2_m	Y-linked autoimmune acceleration 2 (mouse)	qtl	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9743333
1301616	Yaa2_m	Y-linked autoimmune acceleration 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9743333
1301616	Yaa2_m	Y-linked autoimmune acceleration 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9743333
1301618	Bglu1_m	blood glucose level 1 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:10894496
1301618	Bglu1_m	blood glucose level 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10894496
1301620	Insq8_m	insulin QTL 8 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10871196
1301620	Insq8_m	insulin QTL 8 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10871196
1301622	Eae12_m	susceptibility to experimental allergic encephalomyelitis 12 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10072563
1301622	Eae12_m	susceptibility to experimental allergic encephalomyelitis 12 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10072563
1301623	Hipp1_m	hippocampal weight 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11331379
1301623	Hipp1_m	hippocampal weight 1 (mouse)	qtl	MP:0008282	enlarged hippocampus		IAGP		N	RGD:5509061	20111116	MGI			PMID:11331379
1301624	Aevm2_m	autoimmune extremity vasculitis in MRL mice 2 (mouse)	qtl	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12746919
1301624	Aevm2_m	autoimmune extremity vasculitis in MRL mice 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12746919
1301624	Aevm2_m	autoimmune extremity vasculitis in MRL mice 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12746919
1301626	Ltsd7_m	lung tumor shape-determining 7 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517788
1301626	Ltsd7_m	lung tumor shape-determining 7 (mouse)	qtl	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517788
1301629	Obq7_m	obesity QTL 7 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210195
1301629	Obq7_m	obesity QTL 7 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210195
1301631	Orgwq7_m	organ weight QTL 7 (mouse)	qtl	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301631	Orgwq7_m	organ weight QTL 7 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301631	Orgwq7_m	organ weight QTL 7 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301631	Orgwq7_m	organ weight QTL 7 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301631	Orgwq7_m	organ weight QTL 7 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301631	Orgwq7_m	organ weight QTL 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12118102
1301631	Orgwq7_m	organ weight QTL 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301631	Orgwq7_m	organ weight QTL 7 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301632	Bw8q1_m	body weight at 8 weeks QTL 1 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12855751
1301632	Bw8q1_m	body weight at 8 weeks QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12855751
1301632	Bw8q1_m	body weight at 8 weeks QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12855751
1301632	Bw8q1_m	body weight at 8 weeks QTL 1 (mouse)	qtl	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12855751
1301634	Eae6a_m	susceptibility to experimental allergic encephalomyelitis 6a (mouse)	qtl	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9712054
1301634	Eae6a_m	susceptibility to experimental allergic encephalomyelitis 6a (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9712054
1301634	Eae6a_m	susceptibility to experimental allergic encephalomyelitis 6a (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10438970
1301634	Eae6a_m	susceptibility to experimental allergic encephalomyelitis 6a (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9712054
1301636	Lith5_m	lithogenic gene 5 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:11842132
1301636	Lith5_m	lithogenic gene 5 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11842132
1301639	Stnn_m	striatal neuron number (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11319941
1301639	Stnn_m	striatal neuron number (mouse)	qtl	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20111116	MGI			PMID:11319941
1301640	Lore4_m	loss of righting induced by ethanol 4 (mouse)	qtl	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1301640	Lore4_m	loss of righting induced by ethanol 4 (mouse)	qtl	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11964553
1301640	Lore4_m	loss of righting induced by ethanol 4 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11964553
1301640	Lore4_m	loss of righting induced by ethanol 4 (mouse)	qtl	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15365296
1301640	Lore4_m	loss of righting induced by ethanol 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11964553
1301641	Sbmd2_m	spinal bone mineral density 2 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:10780854
1301641	Sbmd2_m	spinal bone mineral density 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10780854
1301642	Hdlq20_m	HDL QTL 20 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1301642	Hdlq20_m	HDL QTL 20 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1301643	Melm3_m	melanoma modifier 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11092979
1301643	Melm3_m	melanoma modifier 3 (mouse)	qtl	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20111116	MGI			PMID:11092979
1301643	Melm3_m	melanoma modifier 3 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11092979
1301643	Melm3_m	melanoma modifier 3 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11092979
1301644	Lrnx7_m	learning-contextual 7 (mouse)	qtl	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:11105392
1301644	Lrnx7_m	learning-contextual 7 (mouse)	qtl	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:9354800
1301644	Lrnx7_m	learning-contextual 7 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11105392
1301645	Loca1_m	locomotor activity 1 (mouse)	qtl	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14694905
1301645	Loca1_m	locomotor activity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14694905
1301645	Loca1_m	locomotor activity 1 (mouse)	qtl	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:14694905
1301647	Elpt_m	elevated leptin (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12765967
1301647	Elpt_m	elevated leptin (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12765967
1301647	Elpt_m	elevated leptin (mouse)	qtl	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20201001	MGI			PMID:12765967
1301649	Psl1_m	promotion susceptibility QTL 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9364205
1301649	Psl1_m	promotion susceptibility QTL 1 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9364205
1301649	Psl1_m	promotion susceptibility QTL 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9364205
1301650	Asbb1_m	autoimmune susceptibility in C57BL/6J and BALB/c 1 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:11994421
1301650	Asbb1_m	autoimmune susceptibility in C57BL/6J and BALB/c 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11994421
1301651	Tlf2_m	T lymphocyte fraction 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9754812
1301651	Tlf2_m	T lymphocyte fraction 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9754812
1301651	Tlf2_m	T lymphocyte fraction 2 (mouse)	qtl	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:9754812
1301652	Cpfd2_m	cerebellum pattern fissures (mouse)	qtl	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529272
1301652	Cpfd2_m	cerebellum pattern fissures (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529272
1301653	Obq15_m	obesity QTL 15 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210195
1301653	Obq15_m	obesity QTL 15 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210195
1301655	Bmd12_m	bone mineral density 12 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1301655	Bmd12_m	bone mineral density 12 (mouse)	qtl	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:11450694
1301656	Hpnr5_m	Heligmosomoides polygyrus nematode resistance 5 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301657	Afw2_m	abdominal fat weight QTL 2 (mouse)	qtl	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:9725853
1301657	Afw2_m	abdominal fat weight QTL 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089|PMID:9725853
1301657	Afw2_m	abdominal fat weight QTL 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20141017	MGI		Created by mouse qtl pipeline	PMID:9725853
1301658	Radpf3_m	radiation pulmonary fibrosis 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:12097289
1301658	Radpf3_m	radiation pulmonary fibrosis 3 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12097289
1301658	Radpf3_m	radiation pulmonary fibrosis 3 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12097289
1301659	Arrd2_m	age-related retinal degeneration 2 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20170811	MGI		Created by mouse qtl pipeline	PMID:12766041
1301659	Arrd2_m	age-related retinal degeneration 2 (mouse)	qtl	MP:0031605	decreased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:12766041
1301660	Iba1_m	induction of brown adipocytes 1 (mouse)	qtl	MP:0003012	obsolete no phenotypic analysis		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10931824
1301663	Skull9_m	skull morphology 9 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301663	Skull9_m	skull morphology 9 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301663	Skull9_m	skull morphology 9 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301664	Feml1_m	femur length in high growth mice 1 (mouse)	qtl	MP:0004348	long femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1301664	Feml1_m	femur length in high growth mice 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301664	Feml1_m	femur length in high growth mice 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301666	Eae13_m	susceptibility to experimental allergic encephalomyelitis 13 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10072563
1301666	Eae13_m	susceptibility to experimental allergic encephalomyelitis 13 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10072563
1301667	Lxw5_m	lupus BXSB x NZW 5 (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:14662843
1301667	Lxw5_m	lupus BXSB x NZW 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:14662843
1301667	Lxw5_m	lupus BXSB x NZW 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14662843
1301667	Lxw5_m	lupus BXSB x NZW 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14662843
1301668	nctm2_m	Nakano cataract modifier 2 (mouse)	qtl	MP:0001304	cataract		IAGP		N	RGD:5509061	20111116	MGI			PMID:12470976
1301668	nctm2_m	Nakano cataract modifier 2 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12470976
1301669	Hdlq28_m	HDL QTL 28 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1301669	Hdlq28_m	HDL QTL 28 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1301671	Lorp1_m	loss of righting due to propofol 1 (mouse)	qtl	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20111116	MGI			PMID:9477059
1301671	Lorp1_m	loss of righting due to propofol 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9477059
1301671	Lorp1_m	loss of righting due to propofol 1 (mouse)	qtl	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20111116	MGI			PMID:9477059
1301672	Lipq1_m	lipoprotein QTL 1 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14722362
1301672	Lipq1_m	lipoprotein QTL 1 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14722362
1301672	Lipq1_m	lipoprotein QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14722362
1301673	Gvhd5_m	graft-versus host disease 5 (mouse)	qtl	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11100271
1301673	Gvhd5_m	graft-versus host disease 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11100271
1301674	Asthm2_m	asthma 2 (mouse)	qtl	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20111116	MGI			PMID:10072427
1301674	Asthm2_m	asthma 2 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10072427
1301676	Nidd6_m	non-insulin-dependent diabetes mellitus 6 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10331427
1301676	Nidd6_m	non-insulin-dependent diabetes mellitus 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331427
1301678	Abpr_m	aberrant B cell proliferation (mouse)	qtl	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:14695357
1301680	Vpantd_m	VPA induced neural tube defect (mouse)	qtl	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20111116	MGI			PMID:15170225
1301680	Vpantd_m	VPA induced neural tube defect (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15170225
1301680	Vpantd_m	VPA induced neural tube defect (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20150302	MGI		Created by mouse qtl pipeline	PMID:15170225
1301680	Vpantd_m	VPA induced neural tube defect (mouse)	qtl	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150305	MGI			PMID:15170225
1301682	Bglq5_m	body growth late QTL 5 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:8846907
1301682	Bglq5_m	body growth late QTL 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10689807
1301685	Estq2_m	estradiol regulated response QTL 2 (mouse)	qtl	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9927277
1301685	Estq2_m	estradiol regulated response QTL 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9927277
1301686	Trmq1_m	T cell ratio modifier QTL 1 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12070778
1301686	Trmq1_m	T cell ratio modifier QTL 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12070778
1301686	Trmq1_m	T cell ratio modifier QTL 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12070778
1301687	Mnic2_m	macronutrient intake (mouse)	qtl	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:12388789
1301687	Mnic2_m	macronutrient intake (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12388789
1301689	Skull18_m	skull morphology 18 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301689	Skull18_m	skull morphology 18 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301689	Skull18_m	skull morphology 18 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301690	Hdlq9_m	HDL QTL 9 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12805272
1301690	Hdlq9_m	HDL QTL 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12805272
1301691	Cdcs10_m	cytokine deficiency colitis susceptibility 10 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11707574
1301691	Cdcs10_m	cytokine deficiency colitis susceptibility 10 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12213197
1301691	Cdcs10_m	cytokine deficiency colitis susceptibility 10 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12213197
1301691	Cdcs10_m	cytokine deficiency colitis susceptibility 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12213197
1301693	Sle6_m	systemic lupus erythematosus susceptibility 6 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1301693	Sle6_m	systemic lupus erythematosus susceptibility 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10485648
1301694	Rear2_m	rearing 2 (mouse)	qtl	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14694905
1301694	Rear2_m	rearing 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14694905
1301696	Wt6q3_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1301696	Wt6q3_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1301697	Sluc18_m	susceptibility to lung cancer 18 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1301697	Sluc18_m	susceptibility to lung cancer 18 (mouse)	qtl	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301697	Sluc18_m	susceptibility to lung cancer 18 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11584065
1301699	Pbwg6_m	postnatal body weight growth 6 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11003694
1301699	Pbwg6_m	postnatal body weight growth 6 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1301699	Pbwg6_m	postnatal body weight growth 6 (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15056934
1301699	Pbwg6_m	postnatal body weight growth 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11003694
1301700	Pctr2_m	plasmacytoma resistance 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8313388
1301700	Pctr2_m	plasmacytoma resistance 2 (mouse)	qtl	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8313388
1301701	Aggr1_m	aggression 1 (mouse)	qtl	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20111116	MGI			PMID:11826145
1301701	Aggr1_m	aggression 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11826145
1301703	Bomd3_m	bone mineral density 3 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11697791
1301703	Bomd3_m	bone mineral density 3 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11697792
1301703	Bomd3_m	bone mineral density 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11697792
1301704	Dbsty1_m	diabesity 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11042154
1301704	Dbsty1_m	diabesity 1 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11042154
1301704	Dbsty1_m	diabesity 1 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11042154
1301704	Dbsty1_m	diabesity 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11042154
1301704	Dbsty1_m	diabesity 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11042154
1301705	Sles3_m	systemic lupus erythmatosus suppressor 3 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1301705	Sles3_m	systemic lupus erythmatosus suppressor 3 (mouse)	qtl	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1301705	Sles3_m	systemic lupus erythmatosus suppressor 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10485648
1301706	Cdcs6_m	cytokine deficiency colitis susceptibility 6 (mouse)	qtl	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11707574
1301706	Cdcs6_m	cytokine deficiency colitis susceptibility 6 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1301706	Cdcs6_m	cytokine deficiency colitis susceptibility 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11707574
1301707	Mwq3_m	molecular weight of quadriceps QTL 3 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1301707	Mwq3_m	molecular weight of quadriceps QTL 3 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12568393
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:14667144
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20111116	MGI			PMID:17371164
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694|PMID:12568393
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694|PMID:12568393
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694|PMID:12568393
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20111215	MGI			PMID:12568393
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20220922	MGI			PMID:14667144
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:12568393
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1301710	Bmd5_m	bone mineral density 5 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:12568393
1301711	Tbrs3_m	tuberculosis resistance 3 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11197687
1301711	Tbrs3_m	tuberculosis resistance 3 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12740444
1301711	Tbrs3_m	tuberculosis resistance 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11197687
1301712	Idd9.1_m	insulin dependent diabetes susceptibility 9.1 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10933399
1301712	Idd9.1_m	insulin dependent diabetes susceptibility 9.1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10933399
1301712	Idd9.1_m	insulin dependent diabetes susceptibility 9.1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10933399
1301712	Idd9.1_m	insulin dependent diabetes susceptibility 9.1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10933399
1301712	Idd9.1_m	insulin dependent diabetes susceptibility 9.1 (mouse)	qtl	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1301713	Dbsty2_m	diabesity 2 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11042154
1301713	Dbsty2_m	diabesity 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11042154
1301714	Vertcling_m	vertical clinging (mouse)	qtl	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1301714	Vertcling_m	vertical clinging (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1301715	Elmaz2_m	elevated maze behavior 2 (mouse)	qtl	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20111116	MGI			PMID:11420611
1301715	Elmaz2_m	elevated maze behavior 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11420611
1301716	Aeyo_m	age of eyelid opening (mouse)	qtl	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1301716	Aeyo_m	age of eyelid opening (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1301717	Adip4_m	adiposity 4 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301717	Adip4_m	adiposity 4 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301717	Adip4_m	adiposity 4 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301717	Adip4_m	adiposity 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301718	Pbw3_m	pentobarbital withdrawal QTL 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529278|PMID:16436183
1301718	Pbw3_m	pentobarbital withdrawal QTL 3 (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529278
1301718	Pbw3_m	pentobarbital withdrawal QTL 3 (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:16436183
1301720	Hpnr8_m	Heligmosomoides polygyrus nematode resistance 8 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301721	Lipq3_m	lipoprotein QTL 3 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14722362
1301721	Lipq3_m	lipoprotein QTL 3 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14722362
1301721	Lipq3_m	lipoprotein QTL 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14722362
1301722	Cia9_m	collagen induced arthritis QTL 9 (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11433381
1301722	Cia9_m	collagen induced arthritis QTL 9 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11433381
1301722	Cia9_m	collagen induced arthritis QTL 9 (mouse)	qtl	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11433381
1301722	Cia9_m	collagen induced arthritis QTL 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11433381
1301723	Fcsa7_m	femoral cross-sectional area 7 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1301723	Fcsa7_m	femoral cross-sectional area 7 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1301723	Fcsa7_m	femoral cross-sectional area 7 (mouse)	qtl	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12369778
1301724	Pcd4ts1_m	p-glycoprotein positive CD4 T cell subset 1 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301724	Pcd4ts1_m	p-glycoprotein positive CD4 T cell subset 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301724	Pcd4ts1_m	p-glycoprotein positive CD4 T cell subset 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301725	Lifespan1_m	life span 1 (mouse)	qtl	MP:0001661	extended life span		IAGP		N	RGD:5509061	20111116	MGI			PMID:11773201
1301725	Lifespan1_m	life span 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11773201
1301726	Tlq1_m	telomere length QTL 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9671732
1301726	Tlq1_m	telomere length QTL 1 (mouse)	qtl	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20230824	MGI			PMID:9671732
1301726	Tlq1_m	telomere length QTL 1 (mouse)	qtl	MP:0030928	increased telomere length		IAGP		N	RGD:5509061	20230824	MGI			PMID:9671732
1301728	Ffal1_m	free fatty acid level 1 (mouse)	qtl	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12925895
1301728	Ffal1_m	free fatty acid level 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12925895
1301730	Szv3_m	seizure severity 3 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:11472065
1301730	Szv3_m	seizure severity 3 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301730	Szv3_m	seizure severity 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301733	Heal3_m	wound healing/regeneration 3 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:9751744
1301733	Heal3_m	wound healing/regeneration 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777|PMID:9751744
1301733	Heal3_m	wound healing/regeneration 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:9751744
1301734	Acsns2_m	Angiostrongylus costaricensis nematode susceptibility 2 (mouse)	qtl	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11862393
1301734	Acsns2_m	Angiostrongylus costaricensis nematode susceptibility 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11862393
1301737	Insq9_m	insulin QTL 9 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10871196
1301737	Insq9_m	insulin QTL 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10871196
1301738	Rhs1_m	resistance to herpes simplex virus 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11342599
1301738	Rhs1_m	resistance to herpes simplex virus 1 (mouse)	qtl	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11342599
1301739	Pitm2_m	prion incubation time 2 (mouse)	qtl	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11404459
1301739	Pitm2_m	prion incubation time 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11404459
1301740	Bwq2_m	body weight QTL 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15472465
1301740	Bwq2_m	body weight QTL 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:18227763
1301740	Bwq2_m	body weight QTL 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9657845
1301740	Bwq2_m	body weight QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9657845
1301740	Bwq2_m	body weight QTL 2 (mouse)	qtl	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20111116	MGI			PMID:15472465
1301741	Lith2_m	lithogenic gene 2 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:11074014
1301741	Lith2_m	lithogenic gene 2 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11074014
1301742	Tnfp_m	tumor necrosis factor protection (mouse)	qtl	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20111116	MGI			PMID:10049582
1301742	Tnfp_m	tumor necrosis factor protection (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10049582
1301744	Hdlq11_m	HDL QTL 11 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12588951
1301744	Hdlq11_m	HDL QTL 11 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12588951
1301747	Eae21_m	experimental allergic encephalomyelitis 21 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10934166
1301747	Eae21_m	experimental allergic encephalomyelitis 21 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1301747	Eae21_m	experimental allergic encephalomyelitis 21 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1301747	Eae21_m	experimental allergic encephalomyelitis 21 (mouse)	qtl	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:10934166
1301748	Abbp1_m	A/J and C57BL/6 blood pressure 1 (mouse)	qtl	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20111116	MGI			PMID:14612590
1301748	Abbp1_m	A/J and C57BL/6 blood pressure 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14612590
1301749	Orgwq1_m	organ weight QTL 1 (mouse)	qtl	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301749	Orgwq1_m	organ weight QTL 1 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301749	Orgwq1_m	organ weight QTL 1 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301749	Orgwq1_m	organ weight QTL 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301749	Orgwq1_m	organ weight QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12118102
1301749	Orgwq1_m	organ weight QTL 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301749	Orgwq1_m	organ weight QTL 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301749	Orgwq1_m	organ weight QTL 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301754	Cocia5_m	cocaine induced activation 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1301754	Cocia5_m	cocaine induced activation 5 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301754	Cocia5_m	cocaine induced activation 5 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301755	Hrq1_m	heart rate quantitative locus 1 (mouse)	qtl	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118100
1301755	Hrq1_m	heart rate quantitative locus 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118100
1301756	Pgia1_m	proteoglycan induced arthritis 1 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1301756	Pgia1_m	proteoglycan induced arthritis 1 (mouse)	qtl	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1301756	Pgia1_m	proteoglycan induced arthritis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997|PMID:15084914
1301756	Pgia1_m	proteoglycan induced arthritis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:10615997
1301758	Fcsa3_m	femoral cross-sectional area 3 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1301758	Fcsa3_m	femoral cross-sectional area 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1301758	Fcsa3_m	femoral cross-sectional area 3 (mouse)	qtl	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12369778
1301759	Sles1_m	systemic lupus erythmatosus suppressor 1 (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1301759	Sles1_m	systemic lupus erythmatosus suppressor 1 (mouse)	qtl	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:16002707
1301759	Sles1_m	systemic lupus erythmatosus suppressor 1 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1301759	Sles1_m	systemic lupus erythmatosus suppressor 1 (mouse)	qtl	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1301759	Sles1_m	systemic lupus erythmatosus suppressor 1 (mouse)	qtl	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:16002707
1301759	Sles1_m	systemic lupus erythmatosus suppressor 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10485648
1301759	Sles1_m	systemic lupus erythmatosus suppressor 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:10485648
1301762	Nidd2n_m	non-insulin-dependent diabetes mellitus 2 in NSY (mouse)	qtl	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:10331425
1301762	Nidd2n_m	non-insulin-dependent diabetes mellitus 2 in NSY (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331425
1301764	Chab4_m	cholesterol absorption 4 (mouse)	qtl	MP:0002646	increased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20111116	MGI			PMID:11714849
1301764	Chab4_m	cholesterol absorption 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301764	Chab4_m	cholesterol absorption 4 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301765	Skull15_m	skull morphology 15 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301765	Skull15_m	skull morphology 15 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301765	Skull15_m	skull morphology 15 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301766	Desp1_m	despair 1 (mouse)	qtl	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20111116	MGI			PMID:11875023
1301766	Desp1_m	despair 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11875023
1301767	Fcsa2_m	femoral cross-sectional area 2 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1301767	Fcsa2_m	femoral cross-sectional area 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1301767	Fcsa2_m	femoral cross-sectional area 2 (mouse)	qtl	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12369778
1301768	Bw14_m	body weight QTL 14 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1301768	Bw14_m	body weight QTL 14 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1301769	Orgwq2_m	organ weight QTL 2 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301769	Orgwq2_m	organ weight QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12118102
1301769	Orgwq2_m	organ weight QTL 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301769	Orgwq2_m	organ weight QTL 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301771	Pcyts6_m	plasmacytoma susceptibility 6 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12149518
1301771	Pcyts6_m	plasmacytoma susceptibility 6 (mouse)	qtl	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12149518
1301772	Skull3_m	skull morphology 3 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301772	Skull3_m	skull morphology 3 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301772	Skull3_m	skull morphology 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301773	Stheal7_m	soft tissue heal 7 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11731492
1301773	Stheal7_m	soft tissue heal 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11731492
1301775	Hdis_m	horizontal distance traveled (mouse)	qtl	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:14694905
1301775	Hdis_m	horizontal distance traveled (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14694905
1301779	Dpml_m	dopamine loss (mouse)	qtl	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12967986
1301779	Dpml_m	dopamine loss (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12967986
1301779	Dpml_m	dopamine loss (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12967986
1301780	Tir3_m	trypanosome infection response 3 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15859356
1301780	Tir3_m	trypanosome infection response 3 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:18253157
1301780	Tir3_m	trypanosome infection response 3 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9171834
1301780	Tir3_m	trypanosome infection response 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9171834
1301781	Capsq3_m	capsaicin sensitivity related QTL 3 (mouse)	qtl	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14499433
1301781	Capsq3_m	capsaicin sensitivity related QTL 3 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14499433
1301782	Chol11_m	cholesterol 11 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14872007
1301782	Chol11_m	cholesterol 11 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14872007
1301783	Bhr1_m	bronchial hyperresponsiveness 1 (mouse)	qtl	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20111116	MGI			PMID:15657107
1301783	Bhr1_m	bronchial hyperresponsiveness 1 (mouse)	qtl	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20111116	MGI			PMID:7550342
1301783	Bhr1_m	bronchial hyperresponsiveness 1 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7550342
1301784	Ses2_m	salmonella enteritidis susceptibility 2 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12058254
1301784	Ses2_m	salmonella enteritidis susceptibility 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058254
1301785	Lmblgq1_m	limb length QTL 1 (mouse)	qtl	MP:0002764	short tibia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301785	Lmblgq1_m	limb length QTL 1 (mouse)	qtl	MP:0003109	short femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301785	Lmblgq1_m	limb length QTL 1 (mouse)	qtl	MP:0004351	short humerus		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301785	Lmblgq1_m	limb length QTL 1 (mouse)	qtl	MP:0004359	short ulna		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301785	Lmblgq1_m	limb length QTL 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301785	Lmblgq1_m	limb length QTL 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301786	Bpq3_m	blood pressure QTL 3 (mouse)	qtl	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20111116	MGI			PMID:11161799
1301786	Bpq3_m	blood pressure QTL 3 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11161799
1301787	Bsc1_m	brain size control 1 (mouse)	qtl	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11319941
1301787	Bsc1_m	brain size control 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11319941
1301787	Bsc1_m	brain size control 1 (mouse)	qtl	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11319941
1301788	Lbw8_m	lupus NZB x NZW 8 (mouse)	qtl	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20111116	MGI			PMID:7937857
1301788	Lbw8_m	lupus NZB x NZW 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1301789	Pbwg4_m	postnatal body weight growth 4 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1301789	Pbwg4_m	postnatal body weight growth 4 (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15056934
1301789	Pbwg4_m	postnatal body weight growth 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15056934
1301791	Char4_m	P. chabaudi malaria resistance QTL 4 (mouse)	qtl	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14595440
1301791	Char4_m	P. chabaudi malaria resistance QTL 4 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11535821
1301791	Char4_m	P. chabaudi malaria resistance QTL 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11535821
1301791	Char4_m	P. chabaudi malaria resistance QTL 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11535821
1301792	Hdlq10_m	HDL QTL 10 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12588951
1301792	Hdlq10_m	HDL QTL 10 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14701919
1301792	Hdlq10_m	HDL QTL 10 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14701919|PMID:12588951|PMID:16685081
1301792	Hdlq10_m	HDL QTL 10 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:12588951
1301795	Cbm3_m	cerebellum weight 3 (mouse)	qtl	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11438585
1301795	Cbm3_m	cerebellum weight 3 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11438585
1301796	Mop2_m	morphine preference 2 (mouse)	qtl	MP:0002553	preference for addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:15508023
1301796	Mop2_m	morphine preference 2 (mouse)	qtl	MP:0002553	preference for addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:8075641
1301796	Mop2_m	morphine preference 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8075641
1301797	Idd1_m	insulin dependent diabetes susceptibility 1 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:2576007
1301797	Idd1_m	insulin dependent diabetes susceptibility 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8661724|PMID:2576007
1301797	Idd1_m	insulin dependent diabetes susceptibility 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8661724|PMID:2576007
1301797	Idd1_m	insulin dependent diabetes susceptibility 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8661724|PMID:2576007
1301797	Idd1_m	insulin dependent diabetes susceptibility 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8661724|PMID:2576007
1301797	Idd1_m	insulin dependent diabetes susceptibility 1 (mouse)	qtl	MP:0005580	periinsulitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8661724
1301797	Idd1_m	insulin dependent diabetes susceptibility 1 (mouse)	qtl	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:15309345
1301798	Hdlq31_m	HDL QTL 31 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1301798	Hdlq31_m	HDL QTL 31 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1301801	Cpfd5_m	cerebellum pattern fissures (mouse)	qtl	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529272
1301801	Cpfd5_m	cerebellum pattern fissures (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529272
1301802	Bglq8_m	body growth late QTL 8 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:8846907
1301802	Bglq8_m	body growth late QTL 8 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8846907
1301803	Stheal9_m	soft tissue heal 9 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11731492
1301803	Stheal9_m	soft tissue heal 9 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:16341671
1301803	Stheal9_m	soft tissue heal 9 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:18028142
1301803	Stheal9_m	soft tissue heal 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16341671|PMID:11731492
1301803	Stheal9_m	soft tissue heal 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:11731492
1301804	Bulb2_m	bulb size 2 (mouse)	qtl	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529276
1301804	Bulb2_m	bulb size 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529276
1301805	Mors2_m	modifier of obesity related sterility 2 (mouse)	qtl	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20111116	MGI			PMID:9927300
1301805	Mors2_m	modifier of obesity related sterility 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9927300
1301806	Actd2_m	activity-distance traveled 2 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:11105390
1301806	Actd2_m	activity-distance traveled 2 (mouse)	qtl	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:11105390
1301806	Actd2_m	activity-distance traveled 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11105390
1301807	Alcp19_m	alcohol preference locus 19 (mouse)	qtl	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:9880655
1301807	Alcp19_m	alcohol preference locus 19 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880655
1301808	Nhdlq1_m	non-HDL QTL 1 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14701919
1301808	Nhdlq1_m	non-HDL QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844|PMID:14701919
1301808	Nhdlq1_m	non-HDL QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	PMID:14701919
1301809	Axtofd1_m	anxiety-open field defecation 1 (mouse)	qtl	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:14990867
1301809	Axtofd1_m	anxiety-open field defecation 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769|PMID:14990867
1301809	Axtofd1_m	anxiety-open field defecation 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11454769
1301812	Hpnr3_m	Heligmosomoides polygyrus nematode resistance 3 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301812	Hpnr3_m	Heligmosomoides polygyrus nematode resistance 3 (mouse)	qtl	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12647241
1301812	Hpnr3_m	Heligmosomoides polygyrus nematode resistance 3 (mouse)	qtl	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301813	Skl3_m	skeletal size (tail length) 3 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301813	Skl3_m	skeletal size (tail length) 3 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301815	Sles2_m	systemic lupus erythmatosus suppressor 2 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1301815	Sles2_m	systemic lupus erythmatosus suppressor 2 (mouse)	qtl	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485648
1301815	Sles2_m	systemic lupus erythmatosus suppressor 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10485648
1301816	Cocia7_m	cocaine induced activation 7 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1301816	Cocia7_m	cocaine induced activation 7 (mouse)	qtl	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301816	Cocia7_m	cocaine induced activation 7 (mouse)	qtl	MP:0020871	abnormal locomotor response to cocaine		IAGP		N	RGD:5509061	20220421	MGI			PMID:12777963
1301818	Ap1q_m	alcohol preference 1 QTL (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:9726281
1301818	Ap1q_m	alcohol preference 1 QTL (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9726281
1301820	Mop1_m	morphine preference 1 (mouse)	qtl	MP:0002553	preference for addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:8075641
1301820	Mop1_m	morphine preference 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8075641
1301821	Tapr_m	T-cell and airway phenotype regulator (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11725301
1301821	Tapr_m	T-cell and airway phenotype regulator (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11725301
1301822	Pgia2_m	proteoglycan induced arthritis 2 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1301822	Pgia2_m	proteoglycan induced arthritis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:12490544
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:14667144
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20220923	MGI		Created by mouse qtl pipeline	PMID:11450694
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:12568393
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:12490544
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0021183	increased femoral compact bone area		IAGP		N	RGD:5509061	20220922	MGI			PMID:14667144
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1301823	Bmd7_m	bone mineral density 7 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:12568393
1301824	Susp_m	suppressor of superoxide production (mouse)	qtl	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20111116	MGI			PMID:11937300
1301824	Susp_m	suppressor of superoxide production (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937300
1301825	Pbrgcsf1_m	peripheral blood stem cell response to granulocyte colony stimulating factor 1 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14725902
1301825	Pbrgcsf1_m	peripheral blood stem cell response to granulocyte colony stimulating factor 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10688851
1301826	Pgia3_m	proteoglycan induced arthritis 3 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1301826	Pgia3_m	proteoglycan induced arthritis 3 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1301826	Pgia3_m	proteoglycan induced arthritis 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997
1301828	Insq5_m	insulin QTL 5 (mouse)	qtl	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1301828	Insq5_m	insulin QTL 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11109545
1301829	Thyls2_m	thymic lymphoma susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14514657
1301829	Thyls2_m	thymic lymphoma susceptibility 2 (mouse)	qtl	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20111215	MGI			PMID:14514657
1301829	Thyls2_m	thymic lymphoma susceptibility 2 (mouse)	qtl	MP:0004503	decreased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:14514657
1301829	Thyls2_m	thymic lymphoma susceptibility 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20260102	MGI		Created by mouse qtl pipeline	PMID:14514657
1301829	Thyls2_m	thymic lymphoma susceptibility 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:14514657
1301829	Thyls2_m	thymic lymphoma susceptibility 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:14514657
1301829	Thyls2_m	thymic lymphoma susceptibility 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:14514657
1301832	Bw17_m	body weight QTL 17 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1301832	Bw17_m	body weight QTL 17 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1301832	Bw17_m	body weight QTL 17 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11109545
1301834	Bits1_m	bitterness sensitivity 1 (mouse)	qtl	MP:0004210	abnormal bitter taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:10609087
1301834	Bits1_m	bitterness sensitivity 1 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10609087
1301835	Carp3_m	carcass protein in high growth mice 3 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1301835	Carp3_m	carcass protein in high growth mice 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301836	Heal5_m	wound healing/regeneration 5 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:12682777
1301836	Heal5_m	wound healing/regeneration 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777
1301837	Alcw2_m	alcohol withdrawal 2 (mouse)	qtl	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:18815268
1301837	Alcw2_m	alcohol withdrawal 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9133412
1301837	Alcw2_m	alcohol withdrawal 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9133412
1301837	Alcw2_m	alcohol withdrawal 2 (mouse)	qtl	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20111116	MGI			PMID:18815268
1301837	Alcw2_m	alcohol withdrawal 2 (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:12893462
1301837	Alcw2_m	alcohol withdrawal 2 (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:14960011
1301837	Alcw2_m	alcohol withdrawal 2 (mouse)	qtl	MP:0009776	decreased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11978849
1301837	Alcw2_m	alcohol withdrawal 2 (mouse)	qtl	MP:0009776	decreased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:14960011
1301837	Alcw2_m	alcohol withdrawal 2 (mouse)	qtl	MP:0009776	decreased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:18815268
1301838	Sluc16_m	susceptibility to lung cancer 16 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1301838	Sluc16_m	susceptibility to lung cancer 16 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1301840	Ssial4_m	susceptibility to sialadenitiss 4 (mouse)	qtl	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11937580
1301840	Ssial4_m	susceptibility to sialadenitiss 4 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1301840	Ssial4_m	susceptibility to sialadenitiss 4 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1301840	Ssial4_m	susceptibility to sialadenitiss 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11937580
1301841	Lrnx9_m	learning-contextual 9 (mouse)	qtl	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:9354800
1301841	Lrnx9_m	learning-contextual 9 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9354800
1301842	Gvhd4_m	graft-versus host disease 4 (mouse)	qtl	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11100271
1301842	Gvhd4_m	graft-versus host disease 4 (mouse)	qtl	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11100271
1301842	Gvhd4_m	graft-versus host disease 4 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11100271
1301842	Gvhd4_m	graft-versus host disease 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11100271
1301843	Listr1_m	listeriosis resistance 1 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11242105
1301843	Listr1_m	listeriosis resistance 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11242105
1301845	Lxw4_m	lupus BXSB x NZW 4 (mouse)	qtl	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20111116	MGI			PMID:14662843
1301845	Lxw4_m	lupus BXSB x NZW 4 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14662843
1301847	Fecq2_m	fecundity QTL 2 (mouse)	qtl	MP:0001934	increased litter size		IAGP		N	RGD:5509061	20111116	MGI			PMID:9457667
1301847	Fecq2_m	fecundity QTL 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9457667
1301849	Derm1_m	dermititis 1 (mouse)	qtl	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11261926
1301849	Derm1_m	dermititis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11261926
1301849	Derm1_m	dermititis 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11261926
1301850	Fglu_m	fasting glucose (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:9916873
1301850	Fglu_m	fasting glucose (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9916873
1301851	Tria5_m	T-cell receptor induced activation 5 (mouse)	qtl	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10384038
1301851	Tria5_m	T-cell receptor induced activation 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10384038
1301851	Tria5_m	T-cell receptor induced activation 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:10384038
1301852	Ltry_m	laterality (mouse)	qtl	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20111116	MGI			PMID:12663540
1301852	Ltry_m	laterality (mouse)	qtl	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12663540
1301852	Ltry_m	laterality (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12663540
1301852	Ltry_m	laterality (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12663540
1301853	Heal9_m	wound healing/regeneration 9 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:12682777
1301853	Heal9_m	wound healing/regeneration 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777
1301858	Smdq1_m	segregation of mitochondrial DNA QTL 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12539044
1301858	Smdq1_m	segregation of mitochondrial DNA QTL 1 (mouse)	qtl	MP:0006037	abnormal mitochondrial fission		IAGP		N	RGD:5509061	20111116	MGI			PMID:12539044
1301861	Scpro2_m	stem cell proliferation 2 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10094931
1301861	Scpro2_m	stem cell proliferation 2 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12200366
1301861	Scpro2_m	stem cell proliferation 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10094931
1301861	Scpro2_m	stem cell proliferation 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10094931
1301862	Tchol1_m	total cholesterol level 1 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11473059
1301862	Tchol1_m	total cholesterol level 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11473059
1301863	Skull5_m	skull morphology 5 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301863	Skull5_m	skull morphology 5 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301863	Skull5_m	skull morphology 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301864	Afw9_m	abdominal fat weight QTL 9 (mouse)	qtl	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1301864	Afw9_m	abdominal fat weight QTL 9 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1301865	Hdlq19_m	HDL QTL 19 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1301865	Hdlq19_m	HDL QTL 19 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18048852
1301865	Hdlq19_m	HDL QTL 19 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847|PMID:18048852
1301865	Hdlq19_m	HDL QTL 19 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:14592847
1301866	Cplaq3_m	circadian period of locomotor activity 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14667146|PMID:8917949|PMID:10547923
1301867	Idd11_m	insulin dependent diabetes susceptibility 11 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8016086
1301867	Idd11_m	insulin dependent diabetes susceptibility 11 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8016086|PMID:15814708
1301868	Fbgl1_m	fasting blood glucose 1 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11473059
1301868	Fbgl1_m	fasting blood glucose 1 (mouse)	qtl	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20111116	MGI			PMID:15769825
1301868	Fbgl1_m	fasting blood glucose 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11473059
1301868	Fbgl1_m	fasting blood glucose 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11473059
1301871	Frp1_m	free running period 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11381025
1301871	Frp1_m	free running period 1 (mouse)	qtl	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:11381025
1301872	Cd4ts3_m	CD4 T cell subset 3 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12595899
1301872	Cd4ts3_m	CD4 T cell subset 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301872	Cd4ts3_m	CD4 T cell subset 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12595899
1301873	Hsl1_m	hyperoxia susceptibility locus 1 (mouse)	qtl	MP:0002319	hyperoxia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11751202
1301873	Hsl1_m	hyperoxia susceptibility locus 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11751202
1301874	Hdlq16_m	HDL QTL 16 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18772481
1301874	Hdlq16_m	HDL QTL 16 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1301874	Hdlq16_m	HDL QTL 16 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847
1301875	Apmt1_m	accelerator of polyoma-induced mammary tumors 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11003704
1301875	Apmt1_m	accelerator of polyoma-induced mammary tumors 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11003704
1301875	Apmt1_m	accelerator of polyoma-induced mammary tumors 1 (mouse)	qtl	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11003704
1301875	Apmt1_m	accelerator of polyoma-induced mammary tumors 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11003704
1301876	Bits2_m	bitterness sensitivity 2 (mouse)	qtl	MP:0004210	abnormal bitter taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:10609087
1301876	Bits2_m	bitterness sensitivity 2 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10609087
1301877	Bbaa3_m	B.burgdorferi-associated arthritis 3 (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1301877	Bbaa3_m	B.burgdorferi-associated arthritis 3 (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:9916719
1301877	Bbaa3_m	B.burgdorferi-associated arthritis 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9916719
1301879	Insq10_m	insulin QTL 10 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10871196
1301879	Insq10_m	insulin QTL 10 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10871196
1301880	Hypt_m	hypertension (mouse)	qtl	MP:0000231	hypertension		IAGP		N	RGD:5509061	20111116	MGI			PMID:12697907
1301880	Hypt_m	hypertension (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12697907
1301881	Trmq2_m	T cell ratio modifier QTL 2 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12070778
1301881	Trmq2_m	T cell ratio modifier QTL 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12070778
1301881	Trmq2_m	T cell ratio modifier QTL 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12070778
1301882	Etohc2_m	ethanol consumption 2 (mouse)	qtl	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:9880656
1301882	Etohc2_m	ethanol consumption 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9880656
1301883	Skull12_m	skull morphology 12 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301883	Skull12_m	skull morphology 12 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301883	Skull12_m	skull morphology 12 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301884	Musz3_m	muscle size 3 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185459
1301884	Musz3_m	muscle size 3 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185459
1301886	Hdlq24_m	HDL QTL 24 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1301886	Hdlq24_m	HDL QTL 24 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1301887	Nidd4n_m	non-insulin-dependent diabetes mellitus 4 in NSY (mouse)	qtl	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:10331425
1301887	Nidd4n_m	non-insulin-dependent diabetes mellitus 4 in NSY (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331425
1301889	Tcsz3_m	tooth central size 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:11973311
1301889	Tcsz3_m	tooth central size 3 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973311
1301889	Tcsz3_m	tooth central size 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20171006	MGI		Created by mouse qtl pipeline	PMID:11973311
1301889	Tcsz3_m	tooth central size 3 (mouse)	qtl	MP:0030091	macrodontia		IAGP		N	RGD:5509061	20171005	MGI			PMID:11973311
1301890	Adip7_m	adiposity 7 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301890	Adip7_m	adiposity 7 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301891	Alcp25_m	alcohol preference locus 25 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:10443995
1301891	Alcp25_m	alcohol preference locus 25 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10443995
1301892	Szs6_m	seizure susceptibility 6 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:10436030
1301892	Szs6_m	seizure susceptibility 6 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10436030
1301892	Szs6_m	seizure susceptibility 6 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10436030
1301894	Skull2_m	skull morphology 2 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301894	Skull2_m	skull morphology 2 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301894	Skull2_m	skull morphology 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301895	Exq1_m	exploratory and excitability QTL 1 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:10234005
1301895	Exq1_m	exploratory and excitability QTL 1 (mouse)	qtl	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20111116	MGI			PMID:10234005
1301895	Exq1_m	exploratory and excitability QTL 1 (mouse)	qtl	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20111116	MGI			PMID:10234005
1301895	Exq1_m	exploratory and excitability QTL 1 (mouse)	qtl	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:10234005
1301895	Exq1_m	exploratory and excitability QTL 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10234005|PMID:16104379
1301895	Exq1_m	exploratory and excitability QTL 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20151016	MGI		Created by mouse qtl pipeline	PMID:10234005
1301895	Exq1_m	exploratory and excitability QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10234005|PMID:16104379
1301895	Exq1_m	exploratory and excitability QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20151016	MGI		Created by mouse qtl pipeline	PMID:10234005
1301897	Scc2_m	colon tumor susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8944029
1301897	Scc2_m	colon tumor susceptibility 2 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8577718
1301897	Scc2_m	colon tumor susceptibility 2 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8944029
1301901	Im5_m	immunoregulatory 5 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:8962125
1301901	Im5_m	immunoregulatory 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8962125
1301902	Hrtfm4_m	heart failure modifier 4 (mouse)	qtl	MP:0001661	extended life span		IAGP		N	RGD:5509061	20111116	MGI			PMID:14519689
1301902	Hrtfm4_m	heart failure modifier 4 (mouse)	qtl	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20111116	MGI			PMID:14519689
1301902	Hrtfm4_m	heart failure modifier 4 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14519689
1301902	Hrtfm4_m	heart failure modifier 4 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14519689
1301902	Hrtfm4_m	heart failure modifier 4 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14519689
1301903	Tlsm1_m	thymic lymphoma susceptible 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7964490|PMID:9209340
1301903	Tlsm1_m	thymic lymphoma susceptible 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20151113	MGI		Created by mouse qtl pipeline	PMID:9209340
1301903	Tlsm1_m	thymic lymphoma susceptible 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20180406	MGI		Created by mouse qtl pipeline	PMID:7964490
1301903	Tlsm1_m	thymic lymphoma susceptible 1 (mouse)	qtl	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20111215	MGI			PMID:7964490
1301903	Tlsm1_m	thymic lymphoma susceptible 1 (mouse)	qtl	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20111215	MGI			PMID:8641972
1301903	Tlsm1_m	thymic lymphoma susceptible 1 (mouse)	qtl	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20111215	MGI			PMID:9209340
1301903	Tlsm1_m	thymic lymphoma susceptible 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:7964490
1301903	Tlsm1_m	thymic lymphoma susceptible 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:7964490
1301903	Tlsm1_m	thymic lymphoma susceptible 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:7964490
1301904	Iba2_m	induction of brown adipocytes 2 (mouse)	qtl	MP:0003012	obsolete no phenotypic analysis		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10931824
1301907	Rends_m	renal disease susceptibility (mouse)	qtl	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11884477
1301907	Rends_m	renal disease susceptibility (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11884477
1301908	Lrdm2_m	lymphoproliferation (Fas) renal disease modifier 2 (mouse)	qtl	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:1460423
1301908	Lrdm2_m	lymphoproliferation (Fas) renal disease modifier 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1460423
1301908	Lrdm2_m	lymphoproliferation (Fas) renal disease modifier 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1460423
1301909	Smdq2_m	segregation of mitochondrial DNA QTL 2 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12539044
1301909	Smdq2_m	segregation of mitochondrial DNA QTL 2 (mouse)	qtl	MP:0006037	abnormal mitochondrial fission		IAGP		N	RGD:5509061	20111116	MGI			PMID:12539044
1301911	Lbm9_m	lean body mass 9 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1301911	Lbm9_m	lean body mass 9 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1301912	Oriq5_m	ovulation rate QTL 5 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10491617
1301913	Frp3_m	free running period 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11381025
1301913	Frp3_m	free running period 3 (mouse)	qtl	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:11381025
1301914	Ksc1_m	keratinocyte stem cell locus 1 (mouse)	qtl	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12663500
1301914	Ksc1_m	keratinocyte stem cell locus 1 (mouse)	qtl	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14594209
1301914	Ksc1_m	keratinocyte stem cell locus 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12663500
1301915	Chab3_m	cholesterol absorption 3 (mouse)	qtl	MP:0002646	increased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20111116	MGI			PMID:11714849
1301915	Chab3_m	cholesterol absorption 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301915	Chab3_m	cholesterol absorption 3 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301918	Skull22_m	skull morphology 22 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301918	Skull22_m	skull morphology 22 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301918	Skull22_m	skull morphology 22 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301919	Mnek1b_m	modifier of Nek1 (NIMA-related expressed kinase 1 (mouse)	qtl	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20111116	MGI			PMID:10366444
1301919	Mnek1b_m	modifier of Nek1 (NIMA-related expressed kinase 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10366444
1301920	Hpnr7_m	Heligmosomoides polygyrus nematode resistance 7 (mouse)	qtl	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301920	Hpnr7_m	Heligmosomoides polygyrus nematode resistance 7 (mouse)	qtl	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14507332
1301921	Stheal2_m	soft tissue heal 2 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11731492
1301921	Stheal2_m	soft tissue heal 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11731492
1301923	Lith6_m	lithogenic gene 6 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:12810825
1301923	Lith6_m	lithogenic gene 6 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12837957|PMID:12810825
1301923	Lith6_m	lithogenic gene 6 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20150717	MGI		Created by mouse qtl pipeline	PMID:12810825
1301923	Lith6_m	lithogenic gene 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12837957|PMID:12810825
1301924	Bmd10_m	bone mineral density 10 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694|PMID:11957111
1301924	Bmd10_m	bone mineral density 10 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:11450694
1301924	Bmd10_m	bone mineral density 10 (mouse)	qtl	MP:0021186	decreased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:11450694
1301925	Ath6_m	atherosclerosis 6 (mouse)	qtl	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20111116	MGI			PMID:10393218
1301925	Ath6_m	atherosclerosis 6 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10393218
1301926	Adip6_m	adiposity 6 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301926	Adip6_m	adiposity 6 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301926	Adip6_m	adiposity 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301926	Adip6_m	adiposity 6 (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301928	Ltsd3_m	lung tumor shape-determining 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517788
1301928	Ltsd3_m	lung tumor shape-determining 3 (mouse)	qtl	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517788
1301930	Papg1_m	pulmonary adenoma progression 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9331067
1301930	Papg1_m	pulmonary adenoma progression 1 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9331067
1301931	Pas9_m	pulmonary adenoma susceptibility 9 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1301931	Pas9_m	pulmonary adenoma susceptibility 9 (mouse)	qtl	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301931	Pas9_m	pulmonary adenoma susceptibility 9 (mouse)	qtl	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301931	Pas9_m	pulmonary adenoma susceptibility 9 (mouse)	qtl	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1301931	Pas9_m	pulmonary adenoma susceptibility 9 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1301931	Pas9_m	pulmonary adenoma susceptibility 9 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9790761
1301933	Insq6_m	insulin QTL 6 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10871196
1301933	Insq6_m	insulin QTL 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10871196
1301934	Adip2_m	adiposity 2 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301934	Adip2_m	adiposity 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301935	Skull24_m	skull morphology 24 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301935	Skull24_m	skull morphology 24 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301935	Skull24_m	skull morphology 24 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301936	Trigq2_m	triglyceride QTL 2 (mouse)	qtl	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14974682
1301936	Trigq2_m	triglyceride QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14974682
1301937	Skull10_m	skull morphology 10 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301937	Skull10_m	skull morphology 10 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301937	Skull10_m	skull morphology 10 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301940	Carp2_m	carcass protein in high growth mice 2 (mouse)	qtl	MP:0001257	increased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301940	Carp2_m	carcass protein in high growth mice 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301940	Carp2_m	carcass protein in high growth mice 2 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1301940	Carp2_m	carcass protein in high growth mice 2 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301940	Carp2_m	carcass protein in high growth mice 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301940	Carp2_m	carcass protein in high growth mice 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1301940	Carp2_m	carcass protein in high growth mice 2 (mouse)	qtl	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301940	Carp2_m	carcass protein in high growth mice 2 (mouse)	qtl	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1301944	Lmblgq3_m	limb length QTL 3 (mouse)	qtl	MP:0002764	short tibia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301944	Lmblgq3_m	limb length QTL 3 (mouse)	qtl	MP:0003109	short femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301944	Lmblgq3_m	limb length QTL 3 (mouse)	qtl	MP:0004351	short humerus		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301944	Lmblgq3_m	limb length QTL 3 (mouse)	qtl	MP:0004359	short ulna		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1301944	Lmblgq3_m	limb length QTL 3 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301944	Lmblgq3_m	limb length QTL 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1301945	Skl7_m	skeletal size (tail length) 7 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301945	Skl7_m	skeletal size (tail length) 7 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301948	Elsgp3_m	elevated serum gp70 3 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10903778
1301948	Elsgp3_m	elevated serum gp70 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10903778
1301949	Skull20_m	skull morphology 20 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1301949	Skull20_m	skull morphology 20 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301949	Skull20_m	skull morphology 20 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1301950	Otx2m1_m	orthodenticle homolog 2 (Drosophila) modifier 1 (mouse)	qtl	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:12183386
1301950	Otx2m1_m	orthodenticle homolog 2 (Drosophila) modifier 1 (mouse)	qtl	MP:0000088	short mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:12183386
1301950	Otx2m1_m	orthodenticle homolog 2 (Drosophila) modifier 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:12183386
1301950	Otx2m1_m	orthodenticle homolog 2 (Drosophila) modifier 1 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12183386
1301950	Otx2m1_m	orthodenticle homolog 2 (Drosophila) modifier 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12183386
1301951	Eila3_m	ethanol induced locomotor activity 3 (mouse)	qtl	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20111116	MGI			PMID:12931787
1301951	Eila3_m	ethanol induced locomotor activity 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12931787
1301952	Im3_m	immunoregulatory 3 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:9472069
1301952	Im3_m	immunoregulatory 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9472069
1301953	Tmevd9_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 9 (mouse)	qtl	MP:0000921	demyelination		IAGP		N	RGD:5509061	20111116	MGI			PMID:12663542
1301953	Tmevd9_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 9 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12663542
1301955	Amp1_m	amplitude of circadian rhythm 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11381025
1301955	Amp1_m	amplitude of circadian rhythm 1 (mouse)	qtl	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:11381025
1301956	Orch3_m	autoimmune orchitis resistance 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7777570
1301956	Orch3_m	autoimmune orchitis resistance 3 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7777570
1301959	Afw5_m	abdominal fat weight QTL 5 (mouse)	qtl	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:9725853
1301959	Afw5_m	abdominal fat weight QTL 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089|PMID:9725853
1301959	Afw5_m	abdominal fat weight QTL 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20141017	MGI		Created by mouse qtl pipeline	PMID:9725853|PMID:11116089
1301959	Afw5_m	abdominal fat weight QTL 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20141031	MGI		Created by mouse qtl pipeline	PMID:9725853
1301961	Bts1_m	bladder tumor susceptibility 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9879827
1301961	Bts1_m	bladder tumor susceptibility 1 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9879827
1301961	Bts1_m	bladder tumor susceptibility 1 (mouse)	qtl	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:9879827
1301961	Bts1_m	bladder tumor susceptibility 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9879827
1301962	Eila2_m	ethanol induced locomotor activity 2 (mouse)	qtl	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20111116	MGI			PMID:12931787
1301962	Eila2_m	ethanol induced locomotor activity 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12931787
1301964	Bw8q2_m	body weight at 8 weeks QTL 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12855751
1301964	Bw8q2_m	body weight at 8 weeks QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12855751
1301966	Lifespan2_m	life span 2 (mouse)	qtl	MP:0001661	extended life span		IAGP		N	RGD:5509061	20111116	MGI			PMID:11773201
1301966	Lifespan2_m	life span 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11773201
1301967	Hlq4_m	heat loss QTL 4 (mouse)	qtl	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1301967	Hlq4_m	heat loss QTL 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1301968	Estq4_m	estradiol regulated response QTL 4 (mouse)	qtl	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:9927277
1301968	Estq4_m	estradiol regulated response QTL 4 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9927277
1301969	Lbw5_m	lupus NZB x NZW 5 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:7937857
1301969	Lbw5_m	lupus NZB x NZW 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9922399|PMID:7937857
1301969	Lbw5_m	lupus NZB x NZW 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:7937857
1301970	Heal11_m	wound healing/regeneration 11 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:12682777
1301970	Heal11_m	wound healing/regeneration 11 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777
1301971	Cia5_m	collagen induced arthritis QTL 5 (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:9808201
1301971	Cia5_m	collagen induced arthritis QTL 5 (mouse)	qtl	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1301971	Cia5_m	collagen induced arthritis QTL 5 (mouse)	qtl	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1301971	Cia5_m	collagen induced arthritis QTL 5 (mouse)	qtl	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15716976
1301971	Cia5_m	collagen induced arthritis QTL 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280|PMID:15084914|PMID:9808201
1301971	Cia5_m	collagen induced arthritis QTL 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:15611280|PMID:9808201
1301971	Cia5_m	collagen induced arthritis QTL 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280|PMID:15084914|PMID:9808201
1301971	Cia5_m	collagen induced arthritis QTL 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:15611280|PMID:9808201
1301974	Chab7_m	cholesterol absorption 7 (mouse)	qtl	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20111116	MGI			PMID:11714849
1301974	Chab7_m	cholesterol absorption 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301974	Chab7_m	cholesterol absorption 7 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11714849
1301975	Mol1_m	modifier of LPS-response 1 (mouse)	qtl	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10585765
1301975	Mol1_m	modifier of LPS-response 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10585765
1301975	Mol1_m	modifier of LPS-response 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10585765
1301975	Mol1_m	modifier of LPS-response 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10585765
1301977	Szs8_m	seizure susceptibility 8 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11472065
1301977	Szs8_m	seizure susceptibility 8 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301977	Szs8_m	seizure susceptibility 8 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1301978	Tmevd6_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 6 (mouse)	qtl	MP:0000921	demyelination		IAGP		N	RGD:5509061	20111116	MGI			PMID:12663542
1301978	Tmevd6_m	Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 6 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12663542
1301979	Melm1_m	melanoma modifier 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11092979
1301979	Melm1_m	melanoma modifier 1 (mouse)	qtl	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20111116	MGI			PMID:11092979
1301979	Melm1_m	melanoma modifier 1 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11092979
1301979	Melm1_m	melanoma modifier 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11092979
1301980	Fcsa5_m	femoral cross-sectional area 5 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1301980	Fcsa5_m	femoral cross-sectional area 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1301980	Fcsa5_m	femoral cross-sectional area 5 (mouse)	qtl	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12369778
1301981	Aaq1_m	alcohol acceptance QTL 1 (mouse)	qtl	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:9399693
1301981	Aaq1_m	alcohol acceptance QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9399693
1301982	Pltiq1_m	phospholipid transfer protein inducibility QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592843
1301982	Pltiq1_m	phospholipid transfer protein inducibility QTL 1 (mouse)	qtl	MP:0012781	increased phospholipid transfer protein activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:14592843
1301983	Berr2_m	berghei resistance locus 2 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12114535
1301983	Berr2_m	berghei resistance locus 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12114535
1301984	Pbd2_m	peak bone density 2 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:12140680
1301984	Pbd2_m	peak bone density 2 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:17002585
1301984	Pbd2_m	peak bone density 2 (mouse)	qtl	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:12140680
1301984	Pbd2_m	peak bone density 2 (mouse)	qtl	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20111116	MGI			PMID:9922384
1301984	Pbd2_m	peak bone density 2 (mouse)	qtl	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20111116	MGI			PMID:9922384
1301984	Pbd2_m	peak bone density 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11697793
1301986	Bpq4_m	blood pressure QTL 4 (mouse)	qtl	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20111116	MGI			PMID:11161799
1301986	Bpq4_m	blood pressure QTL 4 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11161799
1301988	Bmd11_m	bone mineral density 11 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1301988	Bmd11_m	bone mineral density 11 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1301988	Bmd11_m	bone mineral density 11 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1301988	Bmd11_m	bone mineral density 11 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:12568393
1301989	Hdlq18_m	HDL QTL 18 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18772481
1301989	Hdlq18_m	HDL QTL 18 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1301989	Hdlq18_m	HDL QTL 18 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14872007
1301989	Hdlq18_m	HDL QTL 18 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847|PMID:14872007
1301989	Hdlq18_m	HDL QTL 18 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:14592847
1301990	Arvm1_m	autoimmune renal vasculitis 1 (mouse)	qtl	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10940892
1301990	Arvm1_m	autoimmune renal vasculitis 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10940892
1301990	Arvm1_m	autoimmune renal vasculitis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10940892
1301991	Wta3_m	weight adult 3 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1301991	Wta3_m	weight adult 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1301993	Cocia4_m	cocaine induced activation 4 (mouse)	qtl	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:12777963
1301993	Cocia4_m	cocaine induced activation 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12777963
1301994	Ksc2_m	keratinocyte stem cell locus 2 (mouse)	qtl	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12663500
1301994	Ksc2_m	keratinocyte stem cell locus 2 (mouse)	qtl	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14594209
1301994	Ksc2_m	keratinocyte stem cell locus 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12663500
1301995	Lprm1_m	lymphoproliferation modifier 1 (mouse)	qtl	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9403730
1301995	Lprm1_m	lymphoproliferation modifier 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9403730
1301995	Lprm1_m	lymphoproliferation modifier 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9403730
1301997	Cia7_m	collagen induced arthritis QTL 7 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10453039
1301997	Cia7_m	collagen induced arthritis QTL 7 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:17312155
1301997	Cia7_m	collagen induced arthritis QTL 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10453039
1301997	Cia7_m	collagen induced arthritis QTL 7 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10453039
1301998	Bts2_m	bladder tumor susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9879827
1301998	Bts2_m	bladder tumor susceptibility 2 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9879827
1301998	Bts2_m	bladder tumor susceptibility 2 (mouse)	qtl	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:9879827
1301998	Bts2_m	bladder tumor susceptibility 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9879827
1301999	Lmr15_m	leishmaniasis resistance 15 (mouse)	qtl	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20111116	MGI			PMID:12654824
1301999	Lmr15_m	leishmaniasis resistance 15 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12654824
1301999	Lmr15_m	leishmaniasis resistance 15 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12654824
1301999	Lmr15_m	leishmaniasis resistance 15 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12654824
1301999	Lmr15_m	leishmaniasis resistance 15 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12654824
1301999	Lmr15_m	leishmaniasis resistance 15 (mouse)	qtl	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16511555
1302000	Pgia25_m	proteoglycan induced arthritis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12594249|PMID:12794840
1302000	Pgia25_m	proteoglycan induced arthritis 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12594249|PMID:12794840
1302001	Bdln5_m	body length 5 (mouse)	qtl	MP:0001257	increased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:12856282
1302001	Bdln5_m	body length 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856282
1302003	Sluc17_m	susceptibility to lung cancer 17 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1302003	Sluc17_m	susceptibility to lung cancer 17 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1302004	Lfp2_m	long free running period 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309657
1302004	Lfp2_m	long free running period 2 (mouse)	qtl	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:11309657
1302005	Loco2_m	locomotor activity 2 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:12226705
1302005	Loco2_m	locomotor activity 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12226705
1302006	Szs2_m	seizure susceptibility 2 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9069121
1302006	Szs2_m	seizure susceptibility 2 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9069121
1302006	Szs2_m	seizure susceptibility 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9069121
1302007	Bbaa14_m	B.burgdorferi-associated arthritis 14 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1302007	Bbaa14_m	B.burgdorferi-associated arthritis 14 (mouse)	qtl	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1302007	Bbaa14_m	B.burgdorferi-associated arthritis 14 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1302007	Bbaa14_m	B.burgdorferi-associated arthritis 14 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:11704805
1302008	Gasa4_m	gastritis type A susceptibility locus 4 (mouse)	qtl	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11862406
1302008	Gasa4_m	gastritis type A susceptibility locus 4 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11862406
1302008	Gasa4_m	gastritis type A susceptibility locus 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11862406
1302009	Sbmd1_m	spinal bone mineral density 1 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:10780854
1302009	Sbmd1_m	spinal bone mineral density 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10780854
1302010	Wta1_m	weight adult 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1302010	Wta1_m	weight adult 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1302014	Hdlq23_m	HDL QTL 23 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1302014	Hdlq23_m	HDL QTL 23 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1302015	C10bw2_m	castaneus 10 week body weight 2 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11003694
1302015	C10bw2_m	castaneus 10 week body weight 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11003694
1302016	Ltsd1_m	lung tumor shape-determining 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517788
1302016	Ltsd1_m	lung tumor shape-determining 1 (mouse)	qtl	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517788
1302018	Wt3q2_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1302018	Wt3q2_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1302020	Bbaa20_m	B.burgdorferi-associated arthritis 20 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1302020	Bbaa20_m	B.burgdorferi-associated arthritis 20 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805
1302021	Nidd1n_m	non-insulin-dependent diabetes mellitus 1 in NSY (mouse)	qtl	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:10331425
1302021	Nidd1n_m	non-insulin-dependent diabetes mellitus 1 in NSY (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10331425
1302023	Orch4_m	autoimmune orchitis resistance 4 (mouse)	qtl	MP:0001875	testis inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:7777570
1302023	Orch4_m	autoimmune orchitis resistance 4 (mouse)	qtl	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:7777570
1302023	Orch4_m	autoimmune orchitis resistance 4 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20141219	MGI		Created by mouse qtl pipeline	PMID:7777570
1302023	Orch4_m	autoimmune orchitis resistance 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7777570
1302023	Orch4_m	autoimmune orchitis resistance 4 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7777570
1302024	Skull7_m	skull morphology 7 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1302024	Skull7_m	skull morphology 7 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1302024	Skull7_m	skull morphology 7 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1302025	Pas1_m	pulmonary adenoma susceptibility 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9659579|PMID:7813906|PMID:8499946|PMID:8666392
1302025	Pas1_m	pulmonary adenoma susceptibility 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20151225	MGI		Created by mouse qtl pipeline	PMID:9659579|PMID:8499946|PMID:8666392
1302025	Pas1_m	pulmonary adenoma susceptibility 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20160101	MGI		Created by mouse qtl pipeline	PMID:8499946
1302025	Pas1_m	pulmonary adenoma susceptibility 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:9659579|PMID:7813906|PMID:8499946|PMID:8666392
1302025	Pas1_m	pulmonary adenoma susceptibility 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20151225	MGI		Created by mouse qtl pipeline	PMID:9659579|PMID:8499946|PMID:8666392
1302025	Pas1_m	pulmonary adenoma susceptibility 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:9659579|PMID:7813906|PMID:8499946|PMID:8666392
1302025	Pas1_m	pulmonary adenoma susceptibility 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20151225	MGI		Created by mouse qtl pipeline	PMID:9659579|PMID:8499946|PMID:8666392
1302028	Asbb3_m	autoimmune susceptibility in C57BL/6J and BALB/c 3 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:11994421
1302028	Asbb3_m	autoimmune susceptibility in C57BL/6J and BALB/c 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11994421
1302029	Sst1_m	susceptibility to tuberculosis 1 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10890913
1302029	Sst1_m	susceptibility to tuberculosis 1 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15470055
1302029	Sst1_m	susceptibility to tuberculosis 1 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10890913
1302029	Sst1_m	susceptibility to tuberculosis 1 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20221201	MGI			PMID:34151776
1302029	Sst1_m	susceptibility to tuberculosis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10890913
1302029	Sst1_m	susceptibility to tuberculosis 1 (mouse)	qtl	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20221201	MGI			PMID:34151776
1302029	Sst1_m	susceptibility to tuberculosis 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20221202	MGI		Created by mouse qtl pipeline	PMID:10890913
1302031	Bulb1_m	bulb size 1 (mouse)	qtl	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529276
1302031	Bulb1_m	bulb size 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529276
1302033	Nsv1_m	Neuroadapted Sindbis viral RNA level 1 (mouse)	qtl	MP:0002418	increased susceptibility to viral infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11507212
1302033	Nsv1_m	Neuroadapted Sindbis viral RNA level 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11507212
1302035	Lmb4_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1302035	Lmb4_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20111116	MGI			PMID:17548658
1302035	Lmb4_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20111116	MGI			PMID:9449705
1302035	Lmb4_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9449705
1302035	Lmb4_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449705
1302035	Lmb4_m	lupus in MRL and B6 F2 cross (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9449705
1302037	Nktcn1_m	natural killer T cell numbers 1 (mouse)	qtl	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20111116	MGI			PMID:17237411
1302037	Nktcn1_m	natural killer T cell numbers 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12960309
1302037	Nktcn1_m	natural killer T cell numbers 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12960309
1302037	Nktcn1_m	natural killer T cell numbers 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12960309
1302037	Nktcn1_m	natural killer T cell numbers 1 (mouse)	qtl	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12960309
1302037	Nktcn1_m	natural killer T cell numbers 1 (mouse)	qtl	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:17237411
1302038	Radpf1_m	radiation pulmonary fibrosis 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:9393751
1302038	Radpf1_m	radiation pulmonary fibrosis 1 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9393751
1302038	Radpf1_m	radiation pulmonary fibrosis 1 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12097289
1302038	Radpf1_m	radiation pulmonary fibrosis 1 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9393751
1302039	Oriq4_m	ovulation rate QTL 4 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1302041	Tcsz2_m	tooth central size 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:11973311
1302041	Tcsz2_m	tooth central size 2 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973311
1302041	Tcsz2_m	tooth central size 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20171006	MGI		Created by mouse qtl pipeline	PMID:11973311
1302041	Tcsz2_m	tooth central size 2 (mouse)	qtl	MP:0030091	macrodontia		IAGP		N	RGD:5509061	20171005	MGI			PMID:11973311
1302042	Acsns3_m	Angiostrongylus costaricensis nematode susceptibility 3 (mouse)	qtl	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11862393
1302042	Acsns3_m	Angiostrongylus costaricensis nematode susceptibility 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11862393
1302044	Nss1_m	NOD Sjogren's syndrome 1 (mouse)	qtl	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11782015
1302044	Nss1_m	NOD Sjogren's syndrome 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11782015
1302044	Nss1_m	NOD Sjogren's syndrome 1 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11782015
1302044	Nss1_m	NOD Sjogren's syndrome 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11782015
1302047	Fubi1_m	failure of ureteric bud invasion 1 (mouse)	qtl	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20111116	MGI			PMID:11733383
1302047	Fubi1_m	failure of ureteric bud invasion 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11733383
1302049	Heal1_m	wound healing/regeneration 1 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:9751744
1302049	Heal1_m	wound healing/regeneration 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12682777|PMID:9751744
1302049	Heal1_m	wound healing/regeneration 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:9751744
1302050	Radpf4_m	radiation pulmonary fibrosis 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:12097289
1302050	Radpf4_m	radiation pulmonary fibrosis 4 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12097289
1302050	Radpf4_m	radiation pulmonary fibrosis 4 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12097289
1302054	Gct4_m	granulosa cell tumorigenesis 4 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14678975|PMID:9721880
1302054	Gct4_m	granulosa cell tumorigenesis 4 (mouse)	qtl	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:14678975
1302054	Gct4_m	granulosa cell tumorigenesis 4 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:14678975|PMID:9721880
1302054	Gct4_m	granulosa cell tumorigenesis 4 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:14678975|PMID:9721880
1302054	Gct4_m	granulosa cell tumorigenesis 4 (mouse)	qtl	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20131226	MGI			PMID:9721880
1302054	Gct4_m	granulosa cell tumorigenesis 4 (mouse)	qtl	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20131227	MGI			PMID:14678975
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:9616220
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20111116	MGI			PMID:16873689
1302055	Mob6_m	multigenic obesity 6 (mouse)	qtl	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20120209	MGI			PMID:9616220
1302056	Orgwq4_m	organ weight QTL 4 (mouse)	qtl	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1302056	Orgwq4_m	organ weight QTL 4 (mouse)	qtl	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1302056	Orgwq4_m	organ weight QTL 4 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1302056	Orgwq4_m	organ weight QTL 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12118102
1302056	Orgwq4_m	organ weight QTL 4 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1302058	Hrtfm3_m	heart failure modifier 3 (mouse)	qtl	MP:0001661	extended life span		IAGP		N	RGD:5509061	20111116	MGI			PMID:14519689
1302058	Hrtfm3_m	heart failure modifier 3 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14519689
1302060	El3_m	epilepsy 3 (mouse)	qtl	MP:0002064	seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:8747920
1302060	El3_m	epilepsy 3 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8747920
1302060	El3_m	epilepsy 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8747920
1302061	Szv1_m	seizure severity 1 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:9069121
1302061	Szv1_m	seizure severity 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9069121
1302061	Szv1_m	seizure severity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9069121
1302062	Stheal6_m	soft tissue heal 6 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:11731492
1302062	Stheal6_m	soft tissue heal 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11731492
1302063	Eae19_m	experimental allergic encephalomyelitis 19 (mouse)	qtl	MP:0000921	demyelination		IAGP		N	RGD:5509061	20111116	MGI			PMID:10934166
1302063	Eae19_m	experimental allergic encephalomyelitis 19 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10934166
1302064	Pbwg5_m	postnatal body weight growth 5 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1302064	Pbwg5_m	postnatal body weight growth 5 (mouse)	qtl	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15056934
1302064	Pbwg5_m	postnatal body weight growth 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15056934
1302065	El1_m	epilepsy 1 (mouse)	qtl	MP:0002064	seizures		IAGP		N	RGD:5509061	20111116	MGI			PMID:1871601
1302065	El1_m	epilepsy 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1871601
1302065	El1_m	epilepsy 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:1871601
1302066	Insq2_m	insulin QTL 2 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1302066	Insq2_m	insulin QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11109545
1302067	Scc9_m	colon tumor susceptibility 9 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10485458
1302067	Scc9_m	colon tumor susceptibility 9 (mouse)	qtl	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10485458
1302067	Scc9_m	colon tumor susceptibility 9 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10485458
1302071	Fembrs1_m	femur breaking strength 1 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:11991724
1302071	Fembrs1_m	femur breaking strength 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11991724
1302072	Axtofa7_m	anxiety-open field activity 7 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769|PMID:14990867
1302072	Axtofa7_m	anxiety-open field activity 7 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:11418486|PMID:11454769
1302072	Axtofa7_m	anxiety-open field activity 7 (mouse)	qtl	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:14990867
1302073	Pgct1_m	primordial germ cell tumor locus 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10890890
1302073	Pgct1_m	primordial germ cell tumor locus 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10890890
1302073	Pgct1_m	primordial germ cell tumor locus 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10890890
1302073	Pgct1_m	primordial germ cell tumor locus 1 (mouse)	qtl	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10890890
1302075	Bdln6_m	body length 6 (mouse)	qtl	MP:0001257	increased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:12856282
1302075	Bdln6_m	body length 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856282
1302078	Sluc21_m	susceptibility to lung cancer 21 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1302078	Sluc21_m	susceptibility to lung cancer 21 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1302078	Sluc21_m	susceptibility to lung cancer 21 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1302079	Lbw3_m	lupus NZB x NZW 3 (mouse)	qtl	MP:0002083	premature death		IAGP		N	RGD:5509061	20111116	MGI			PMID:7937857
1302079	Lbw3_m	lupus NZB x NZW 3 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7937857
1302080	Szs13_m	seizure susceptibility 13 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11472065
1302080	Szs13_m	seizure susceptibility 13 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1302080	Szs13_m	seizure susceptibility 13 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1302084	Ckds_m	cystic kidney disease severity (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11773599
1302084	Ckds_m	cystic kidney disease severity (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11773599
1302084	Ckds_m	cystic kidney disease severity (mouse)	qtl	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20111116	MGI			PMID:11773599
1302085	Mobe1_m	modifier of obesity 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:14693723
1302085	Mobe1_m	modifier of obesity 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14693723
1302086	Obq9_m	obesity QTL 9 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11210195
1302086	Obq9_m	obesity QTL 9 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11210195
1302087	Axtofa5_m	anxiety-open field activity 5 (mouse)	qtl	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14990867
1302087	Axtofa5_m	anxiety-open field activity 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11454769|PMID:14990867
1302087	Axtofa5_m	anxiety-open field activity 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160422	MGI		Created by mouse qtl pipeline	PMID:14990867
1302087	Axtofa5_m	anxiety-open field activity 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20160506	MGI		Created by mouse qtl pipeline	PMID:11454769
1302088	Gvhd2_m	graft-versus-host disease 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10233703
1302088	Gvhd2_m	graft-versus-host disease 2 (mouse)	qtl	MP:0005672	increased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20111116	MGI			PMID:10233703
1302089	Wta2_m	weight adult 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1302089	Wta2_m	weight adult 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1302090	Bdt3_m	bone density traits 3 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:16200066
1302090	Bdt3_m	bone density traits 3 (mouse)	qtl	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16200066
1302090	Bdt3_m	bone density traits 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11328966
1302090	Bdt3_m	bone density traits 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11328966
1302090	Bdt3_m	bone density traits 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11328966
1302090	Bdt3_m	bone density traits 3 (mouse)	qtl	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16200066
1302090	Bdt3_m	bone density traits 3 (mouse)	qtl	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16200066
1302092	Ath11_m	atherosclerosis 11 (mouse)	qtl	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11973313
1302092	Ath11_m	atherosclerosis 11 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973313
1302093	Orgwq5_m	organ weight QTL 5 (mouse)	qtl	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1302093	Orgwq5_m	organ weight QTL 5 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1302093	Orgwq5_m	organ weight QTL 5 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1302093	Orgwq5_m	organ weight QTL 5 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1302094	Rrodp1_m	rotarod performance 1 (mouse)	qtl	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20111116	MGI			PMID:14694905
1302094	Rrodp1_m	rotarod performance 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14694905
1302096	Aod1a_m	autoimmune ovarian dysgenesis 1a (mouse)	qtl	MP:0001868	ovary inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12794114
1302096	Aod1a_m	autoimmune ovarian dysgenesis 1a (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12794114
1302096	Aod1a_m	autoimmune ovarian dysgenesis 1a (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12794114
1302096	Aod1a_m	autoimmune ovarian dysgenesis 1a (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12794114
1302098	Eila1_m	ethanol induced locomotor activity 1 (mouse)	qtl	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20111116	MGI			PMID:12931787
1302098	Eila1_m	ethanol induced locomotor activity 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12931787
1302099	Hdlq30_m	HDL QTL 30 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14993241
1302099	Hdlq30_m	HDL QTL 30 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14993241
1302100	Circp2_m	circadian photosensitivity 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12465884
1302100	Circp2_m	circadian photosensitivity 2 (mouse)	qtl	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:12465884
1302102	Bis1_m	beta-carboline-induced seizures 1 (mouse)	qtl	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20111116	MGI			PMID:10234005
1302102	Bis1_m	beta-carboline-induced seizures 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10234005|PMID:7657995
1302102	Bis1_m	beta-carboline-induced seizures 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10234005|PMID:7657995
1302103	Dob2_m	dietary obesity 2 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:7929816
1302103	Dob2_m	dietary obesity 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7929816
1302104	Lfp1_m	long free running period 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309657
1302104	Lfp1_m	long free running period 1 (mouse)	qtl	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:11309657
1302105	Im1_m	Immunoregulatory 1 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:9472069
1302105	Im1_m	Immunoregulatory 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9472069
1302106	Rapop1_m	radiation-induced apoptosis 1 (mouse)	qtl	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9545495
1302106	Rapop1_m	radiation-induced apoptosis 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9545495|PMID:9367689
1302106	Rapop1_m	radiation-induced apoptosis 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:9545495
1302108	Skl5_m	skeletal size (tail length) 5 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1302108	Skl5_m	skeletal size (tail length) 5 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1302108	Skl5_m	skeletal size (tail length) 5 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1302108	Skl5_m	skeletal size (tail length) 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1302109	Sluc28_m	susceptibility to lung cancer 28 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11584065
1302109	Sluc28_m	susceptibility to lung cancer 28 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1302109	Sluc28_m	susceptibility to lung cancer 28 (mouse)	qtl	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:11584065
1302110	Szs12_m	seizure susceptibility 12 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11472065
1302110	Szs12_m	seizure susceptibility 12 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1302110	Szs12_m	seizure susceptibility 12 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1302112	Gct_m	granulosa cell tumorigenesis (mouse)	qtl	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20131226	MGI			PMID:9721880
1302113	Chol5_m	cholesterol 5 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16679719
1302114	Tbs1_m	tuberculosis severity 1 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12496157
1302114	Tbs1_m	tuberculosis severity 1 (mouse)	qtl	MP:0005150	cachexia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12496157
1302114	Tbs1_m	tuberculosis severity 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353873
1302114	Tbs1_m	tuberculosis severity 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353873
1302116	Bbaa1_m	B.burgdorferi-associated arthritis 1 (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:9916719
1302116	Bbaa1_m	B.burgdorferi-associated arthritis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9916719
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11016460
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:8384947
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:16172259
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10857762
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10955330
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11016460
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:1675432
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:18056379
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:8384947
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9257847
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9988264
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:16172259
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0004031	insulitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:18056379
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20111116	MGI			PMID:17277778
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20111116	MGI			PMID:17277778
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20180330	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20180330	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20180330	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20180330	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20180330	MGI		Created by mouse qtl pipeline	PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956
1302117	Idd3_m	insulin dependent diabetes susceptibility 3 (mouse)	qtl	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12759418
1302121	Cliff_m	cliff drop aversion (mouse)	qtl	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1302121	Cliff_m	cliff drop aversion (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1302122	Eae8_m	susceptibility to experimental allergic encephalomyelitis 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9712054|PMID:8757345
1302122	Eae8_m	susceptibility to experimental allergic encephalomyelitis 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20131011	MGI		Created by mouse qtl pipeline	PMID:8757345|PMID:9712054
1302124	Eae7_m	susceptibility to experimental allergic encephalomyelitis 7 (mouse)	qtl	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9712054
1302124	Eae7_m	susceptibility to experimental allergic encephalomyelitis 7 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9712054
1302124	Eae7_m	susceptibility to experimental allergic encephalomyelitis 7 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9712054
1302124	Eae7_m	susceptibility to experimental allergic encephalomyelitis 7 (mouse)	qtl	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9712054
1302124	Eae7_m	susceptibility to experimental allergic encephalomyelitis 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9712054
1302125	Lxw1_m	lupus BXSB x NZW 1 (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:14662843
1302125	Lxw1_m	lupus BXSB x NZW 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14662843
1302126	Skull26_m	skull morphology 26 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1302126	Skull26_m	skull morphology 26 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1302126	Skull26_m	skull morphology 26 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1302127	Hlq3_m	heat loss QTL 3 (mouse)	qtl	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1302127	Hlq3_m	heat loss QTL 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1302128	Ity3_m	immunity to S. typhimurium 3 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:17660555
1302128	Ity3_m	immunity to S. typhimurium 3 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9479490
1302128	Ity3_m	immunity to S. typhimurium 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9479490
1302130	Fembm5_m	femoral bone morphometry 5 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11518254
1302130	Fembm5_m	femoral bone morphometry 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11518254
1302130	Fembm5_m	femoral bone morphometry 5 (mouse)	qtl	MP:0030823	increased femur size		IAGP		N	RGD:5509061	20181018	MGI			PMID:11518254
1302131	Bmd8_m	bone mineral density 8 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12568393
1302131	Bmd8_m	bone mineral density 8 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:14667144
1302131	Bmd8_m	bone mineral density 8 (mouse)	qtl	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:14667144
1302131	Bmd8_m	bone mineral density 8 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1302131	Bmd8_m	bone mineral density 8 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1302131	Bmd8_m	bone mineral density 8 (mouse)	qtl	MP:0013616	decreased volumetric bone mineral density		IAGP		N	RGD:5509061	20220915	MGI			PMID:14667144
1302131	Bmd8_m	bone mineral density 8 (mouse)	qtl	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:11450694
1302131	Bmd8_m	bone mineral density 8 (mouse)	qtl	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:12568393
1302132	Pbw1_m	pentobarbital withdrawal QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10337613
1302132	Pbw1_m	pentobarbital withdrawal QTL 1 (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10337613
1302132	Pbw1_m	pentobarbital withdrawal QTL 1 (mouse)	qtl	MP:0009776	decreased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10337613
1302136	Insq3_m	insulin QTL 3 (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1302136	Insq3_m	insulin QTL 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11109545
1302137	Livq1_m	percent liver QTL 1 (mouse)	qtl	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1302137	Livq1_m	percent liver QTL 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1302137	Livq1_m	percent liver QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10353911
1302138	Im6_m	immunoregulatory 6 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:8962125
1302138	Im6_m	immunoregulatory 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8962125
1302140	Wta4_m	weight adult 4 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11178736
1302140	Wta4_m	weight adult 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11178736
1302141	Fcsa6_m	femoral cross-sectional area 6 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1302141	Fcsa6_m	femoral cross-sectional area 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12369778
1302141	Fcsa6_m	femoral cross-sectional area 6 (mouse)	qtl	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12369778
1302143	Bwq5_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12856282
1302143	Bwq5_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12856282
1302144	Oriq3_m	ovulation rate QTL 3 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1302145	Triglq2_m	triglyceride QTL 2 (mouse)	qtl	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11109545
1302145	Triglq2_m	triglyceride QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11109545
1302147	Skts12_m	skin tumor susceptibility 12 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1302147	Skts12_m	skin tumor susceptibility 12 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:7670492
1302147	Skts12_m	skin tumor susceptibility 12 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1302150	Bbaa18_m	B.burgdorferi-associated arthritis 18 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11704805
1302150	Bbaa18_m	B.burgdorferi-associated arthritis 18 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11704805|PMID:11431140
1302151	Lprm2_m	lymphoproliferation modifier 2 (mouse)	qtl	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10940892
1302151	Lprm2_m	lymphoproliferation modifier 2 (mouse)	qtl	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9403730
1302151	Lprm2_m	lymphoproliferation modifier 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10940892
1302151	Lprm2_m	lymphoproliferation modifier 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10940892
1302152	Skull25_m	skull morphology 25 (mouse)	qtl	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1302152	Skull25_m	skull morphology 25 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1302152	Skull25_m	skull morphology 25 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1302153	Fob1_m	F-line obesity QTL 1 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:10602985
1302153	Fob1_m	F-line obesity QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10602985
1302154	Skmw5_m	skeletal muscle weight 5 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14679300
1302154	Skmw5_m	skeletal muscle weight 5 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14679300
1302157	Bwem2_m	body weight day 30 males 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10086232
1302157	Bwem2_m	body weight day 30 males 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10086232
1302158	Fembrs5_m	femur breaking strength 5 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:11991724
1302158	Fembrs5_m	femur breaking strength 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11991724
1302159	Sle8_m	systematic lupus erythematosus susceptibility 8 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10693874
1302159	Sle8_m	systematic lupus erythematosus susceptibility 8 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10693874
1302159	Sle8_m	systematic lupus erythematosus susceptibility 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10693874
1302160	Mbis2_m	Mycobacterium bovis-induced systemic lupus erythematosus 2 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10903779
1302160	Mbis2_m	Mycobacterium bovis-induced systemic lupus erythematosus 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10903779
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12568393
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:14667144
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:14667144
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11450694
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20220922	MGI			PMID:14667144
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:12568393
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:11450694
1302163	Bmd16_m	bone mineral density 16 (mouse)	qtl	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:12568393
1302164	Psl2_m	promotion susceptibility QTL 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12782578
1302164	Psl2_m	promotion susceptibility QTL 2 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12782578
1302164	Psl2_m	promotion susceptibility QTL 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12782578
1302168	Imgt1_m	impaired glucose tolerance 1 (mouse)	qtl	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:11473059
1302168	Imgt1_m	impaired glucose tolerance 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11473059
1302170	Tanidd1_m	tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15870394
1302170	Tanidd1_m	tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:11414755
1302170	Tanidd1_m	tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11414755
1302170	Tanidd1_m	tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11414755
1302170	Tanidd1_m	tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11414755
1302170	Tanidd1_m	tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse)	qtl	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15870394
1302170	Tanidd1_m	tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse)	qtl	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15870394
1302172	Skts5_m	skin tumor susceptibility 5 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1302172	Skts5_m	skin tumor susceptibility 5 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:10611333
1302172	Skts5_m	skin tumor susceptibility 5 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10611333
1302173	Vent1_m	ventricular size 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12746874
1302173	Vent1_m	ventricular size 1 (mouse)	qtl	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20140220	MGI			PMID:12746874
1302174	Dssc2_m	dextran sodium sulfate induced colitis QTL2 (mouse)	qtl	MP:0002816	colitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9933561
1302174	Dssc2_m	dextran sodium sulfate induced colitis QTL2 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9933561
1302174	Dssc2_m	dextran sodium sulfate induced colitis QTL2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9933561
1302175	Dssc1_m	dextran sodium sulfate induced colitis QTL1 (mouse)	qtl	MP:0002816	colitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9933561
1302175	Dssc1_m	dextran sodium sulfate induced colitis QTL1 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9933561
1302175	Dssc1_m	dextran sodium sulfate induced colitis QTL1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9933561
1302176	Afw1_m	abdominal fat weight QTL 1 (mouse)	qtl	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:9725853
1302176	Afw1_m	abdominal fat weight QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089|PMID:9725853
1302176	Afw1_m	abdominal fat weight QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20141017	MGI		Created by mouse qtl pipeline	PMID:9725853
1302179	Mndl2_m	mandible length 2 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:12161465
1302179	Mndl2_m	mandible length 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:12161465
1302179	Mndl2_m	mandible length 2 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12161465
1302179	Mndl2_m	mandible length 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12161465
1302180	Actd4_m	activity-distance traveled 4 (mouse)	qtl	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:11105390
1302180	Actd4_m	activity-distance traveled 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11105390
1302182	Mob7_m	multigenic obesity 7 (mouse)	qtl	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:9616220
1302183	Pas7_m	pulmonary adenoma susceptibility 7 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1302183	Pas7_m	pulmonary adenoma susceptibility 7 (mouse)	qtl	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1302183	Pas7_m	pulmonary adenoma susceptibility 7 (mouse)	qtl	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:9790761
1302183	Pas7_m	pulmonary adenoma susceptibility 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9790761
1302183	Pas7_m	pulmonary adenoma susceptibility 7 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:9790761
1302184	Aaom1_m	autoimmune aoritis in MRL mice 1 (mouse)	qtl	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12746919
1302184	Aaom1_m	autoimmune aoritis in MRL mice 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12746919
1302184	Aaom1_m	autoimmune aoritis in MRL mice 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12746919
1302185	Pkcal_m	protein kinase C activity in lungs (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10926556
1302185	Pkcal_m	protein kinase C activity in lungs (mouse)	qtl	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20251030	MGI			PMID:10926556
1302186	Blmpf2_m	bleomycin-induced pulmonary fibrosis 2 (mouse)	qtl	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12140188
1302186	Blmpf2_m	bleomycin-induced pulmonary fibrosis 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:12140188
1302186	Blmpf2_m	bleomycin-induced pulmonary fibrosis 2 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12140188
1302186	Blmpf2_m	bleomycin-induced pulmonary fibrosis 2 (mouse)	qtl	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12140188
1302188	Lxw6_m	lupus BXSB x NZW 6 (mouse)	qtl	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20111116	MGI			PMID:14662843
1302188	Lxw6_m	lupus BXSB x NZW 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:14662843
1302188	Lxw6_m	lupus BXSB x NZW 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14662843
1302188	Lxw6_m	lupus BXSB x NZW 6 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14662843
1302191	Mtes1_m	Metastasis efficiency suppressor gene 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11751410|PMID:15859357
1302191	Mtes1_m	Metastasis efficiency suppressor gene 1 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:15859357
1302191	Mtes1_m	Metastasis efficiency suppressor gene 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11751410|PMID:15859357
1302191	Mtes1_m	Metastasis efficiency suppressor gene 1 (mouse)	qtl	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11751410
1302191	Mtes1_m	Metastasis efficiency suppressor gene 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11751410|PMID:15859357
1302192	Tir2_m	trypanosome infection response 2 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:9171834
1302192	Tir2_m	trypanosome infection response 2 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15859356
1302192	Tir2_m	trypanosome infection response 2 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:18253157
1302192	Tir2_m	trypanosome infection response 2 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9171834
1302192	Tir2_m	trypanosome infection response 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9171834|PMID:12847546
1302192	Tir2_m	trypanosome infection response 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20150626	MGI		Created by mouse qtl pipeline	PMID:9171834
1302193	Cpfd1_m	cerebellum pattern fissures (mouse)	qtl	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11529272
1302193	Cpfd1_m	cerebellum pattern fissures (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11529272
1302194	Pgia10_m	proteoglycan induced arthritis 10 (mouse)	qtl	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1302194	Pgia10_m	proteoglycan induced arthritis 10 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:10615997
1302194	Pgia10_m	proteoglycan induced arthritis 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10615997
1302197	Bhr2_m	bronchial hyperresponsiveness 2 (mouse)	qtl	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20111116	MGI			PMID:7550342
1302197	Bhr2_m	bronchial hyperresponsiveness 2 (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7550342
1302198	Lrncs1_m	learning-conditioned stimulus 1 (mouse)	qtl	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:9106670
1302198	Lrncs1_m	learning-conditioned stimulus 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9106670
1302199	Mob3_m	multigenic obesity 3 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:7706460
1302200	Sle12_m	systematic lupus erythematosus susceptibility 12 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9922399
1302200	Sle12_m	systematic lupus erythematosus susceptibility 12 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9922399
1302200	Sle12_m	systematic lupus erythematosus susceptibility 12 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9922399
1302201	Alcw1_m	alcohol withdrawal 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9133412
1302201	Alcw1_m	alcohol withdrawal 1 (mouse)	qtl	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20111116	MGI			PMID:10443995
1302201	Alcw1_m	alcohol withdrawal 1 (mouse)	qtl	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20111116	MGI			PMID:10443995
1302202	Dob3_m	Dietary obesity 3 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:7929816
1302202	Dob3_m	Dietary obesity 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7929816
1302203	Gvhd3_m	graft-versus host disease 3 (mouse)	qtl	MP:0001263	weight loss		IAGP		N	RGD:5509061	20111116	MGI			PMID:10382959
1302203	Gvhd3_m	graft-versus host disease 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10382959
1302204	Spm1_m	splenomegaly modifier (mouse)	qtl	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10607744
1302204	Spm1_m	splenomegaly modifier (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10607744
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190801	MGI			PMID:29360879
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0003279	aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0005412	vascular stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678176
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0009421	increased gastrocnemius weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312051	Sgcb	sarcoglycan, beta (dystrophin-associated glycoprotein)	gene	MP:0009427	increased tibialis anterior weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10441321
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230420	MGI			PMID:27811357
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20250508	MGI			
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17086203
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0002235	abnormal external nares morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0002243	abnormal vomeronasal organ morphology		IAGP		N	RGD:5509061	20230420	MGI			PMID:27811357
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20230420	MGI			PMID:27811357
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0005229	abnormal intervertebral disk development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009654	abnormal primary palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20230420	MGI			PMID:27811357
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20230420	MGI			PMID:27811357
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20221201	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20230420	MGI			PMID:27811357
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009897	decreased maxillary shelf size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0009909	bifid tongue		IAGP		N	RGD:5509061	20230420	MGI			PMID:27811357
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0012523	abnormal upper lip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0013788	external nares atresia		IAGP		N	RGD:5509061	20150611	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0014276	lobar holoprosencephaly		IAGP		N	RGD:5509061	20230810	MGI			PMID:21183473
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230420	MGI			PMID:27811357
1312052	Boc	BOC cell adhesion associated, oncogene regulated	gene	MP:0030314	absent primary palate		IAGP		N	RGD:5509061	20171109	MGI			PMID:21183473
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:19893577
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20160804	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20141003	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20141003	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897489
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897489
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897489
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897489
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20160804	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0005316	abnormal response to tactile stimuli		IEA		N	RGD:5509061	20141003	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897489
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0008210	increased mature B cell number		IEA		N	RGD:5509061	20160804	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0008495	decreased IgG1 level		IEA		N	RGD:5509061	20160804	MGI			
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897489
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1312055	Arhgef4	Rho guanine nucleotide exchange factor 4	gene	MP:0012434	decreased intestinal adenoma incidence		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1312057	Ifi35	interferon-induced protein 35	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1312057	Ifi35	interferon-induced protein 35	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1312057	Ifi35	interferon-induced protein 35	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1312057	Ifi35	interferon-induced protein 35	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1312060	Cog3	component of oligomeric golgi complex 3	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1312060	Cog3	component of oligomeric golgi complex 3	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1312060	Cog3	component of oligomeric golgi complex 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20240523	MGI			
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20250508	MGI			
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20250508	MGI			
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1312064	Pglyrp3	peptidoglycan recognition protein 3	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
1312066	Dstn	destrin	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8603845
1312066	Dstn	destrin	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:8603845
1312066	Dstn	destrin	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875668
1312066	Dstn	destrin	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628996
1312066	Dstn	destrin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1312066	Dstn	destrin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875668
1312066	Dstn	destrin	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1312066	Dstn	destrin	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12700171
1312066	Dstn	destrin	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15855638
1312066	Dstn	destrin	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17051153
1312066	Dstn	destrin	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628996
1312066	Dstn	destrin	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:8603845
1312066	Dstn	destrin	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15855638
1312066	Dstn	destrin	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12700171
1312066	Dstn	destrin	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17051153
1312066	Dstn	destrin	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8603845
1312066	Dstn	destrin	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1312066	Dstn	destrin	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15855638
1312066	Dstn	destrin	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1312066	Dstn	destrin	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312066	Dstn	destrin	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1312066	Dstn	destrin	gene	MP:0020854	increased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:8603845
1312066	Dstn	destrin	gene	MP:0020857	cornea epithelium hyperplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:11182022
1312066	Dstn	destrin	gene	MP:0020857	cornea epithelium hyperplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:12700171
1312068	Wnt6	wingless-type MMTV integration site family, member 6	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175771
1312068	Wnt6	wingless-type MMTV integration site family, member 6	gene	MP:0001727	abnormal embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175771
1312068	Wnt6	wingless-type MMTV integration site family, member 6	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175771
1312068	Wnt6	wingless-type MMTV integration site family, member 6	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175771
1312068	Wnt6	wingless-type MMTV integration site family, member 6	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175771
1312068	Wnt6	wingless-type MMTV integration site family, member 6	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175771
1312068	Wnt6	wingless-type MMTV integration site family, member 6	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20201022	MGI			
1312068	Wnt6	wingless-type MMTV integration site family, member 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170105	MGI			
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11151768
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892475
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892475
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12107726
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11151768
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318952
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892475
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0004130	abnormal muscle cell glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892475
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931681
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931681
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892475
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892475
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931681
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892475
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892475
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0010951	abnormal lipid oxidation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892475
1312071	Tbc1d1	TBC1 domain family, member 1	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:23892475
1312073	Syne3	spectrin repeat containing, nuclear envelope family member 3	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1312073	Syne3	spectrin repeat containing, nuclear envelope family member 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20211125	MGI			PMID:23761073
1312073	Syne3	spectrin repeat containing, nuclear envelope family member 3	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1312075	Rufy2	RUN and FYVE domain-containing 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1312077	Senp6	SUMO/sentrin specific peptidase 6	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1312079	Igsf9	immunoglobulin superfamily, member 9	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1312079	Igsf9	immunoglobulin superfamily, member 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268009
1312079	Igsf9	immunoglobulin superfamily, member 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150212	MGI			PMID:24647940
1312079	Igsf9	immunoglobulin superfamily, member 9	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20150212	MGI			PMID:24647940
1312079	Igsf9	immunoglobulin superfamily, member 9	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1312079	Igsf9	immunoglobulin superfamily, member 9	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24647940
1312079	Igsf9	immunoglobulin superfamily, member 9	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:24647940
1312080	A430005L14Rik	RIKEN cDNA A430005L14 gene	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1312080	A430005L14Rik	RIKEN cDNA A430005L14 gene	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1312080	A430005L14Rik	RIKEN cDNA A430005L14 gene	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1312080	A430005L14Rik	RIKEN cDNA A430005L14 gene	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1312082	P3h2	prolyl 3-hydroxylase 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20200514	MGI			
1312082	P3h2	prolyl 3-hydroxylase 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1312082	P3h2	prolyl 3-hydroxylase 2	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368846
1312082	P3h2	prolyl 3-hydroxylase 2	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25645914
1312082	P3h2	prolyl 3-hydroxylase 2	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1312082	P3h2	prolyl 3-hydroxylase 2	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
1312082	P3h2	prolyl 3-hydroxylase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368846
1312082	P3h2	prolyl 3-hydroxylase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368846
1312082	P3h2	prolyl 3-hydroxylase 2	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368846
1312084	Fem1b	fem 1 homolog b	gene	MP:0000666	decreased prostate gland duct number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18816836
1312084	Fem1b	fem 1 homolog b	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024793
1312084	Fem1b	fem 1 homolog b	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024793
1312084	Fem1b	fem 1 homolog b	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024793
1312090	Mast2	microtubule associated serine/threonine kinase 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1312090	Mast2	microtubule associated serine/threonine kinase 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20150430	MGI			
1312091	Selenon	selenoprotein N	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131290
1312091	Selenon	selenoprotein N	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0001942	abnormal lung volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131290
1312091	Selenon	selenoprotein N	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131290
1312091	Selenon	selenoprotein N	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20141003	MGI			
1312091	Selenon	selenoprotein N	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131290
1312091	Selenon	selenoprotein N	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0009424	decreased extensor digitorum longus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0009426	decreased soleus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0009428	decreased tibialis anterior weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858002
1312091	Selenon	selenoprotein N	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0010902	abnormal pulmonary alveolar sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0011045	decreased lung elastance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312091	Selenon	selenoprotein N	gene	MP:0012107	enhanced exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325319
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265138
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223432
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265138
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223432
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223432
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265138
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223432
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223432
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265138
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223432
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265138
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223432
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223432
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223432
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700190
1312093	Map3k3	mitogen-activated protein kinase kinase kinase 3	gene	MP:0031593	decreased cardiac jelly amount		IAGP		N	RGD:5509061	20240229	MGI			PMID:25625206
1312096	Zfp13	zinc finger protein 13	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1312096	Zfp13	zinc finger protein 13	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20160804	MGI			
1312098	Hsd17b14	hydroxysteroid (17-beta) dehydrogenase 14	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20170413	MGI			
1312098	Hsd17b14	hydroxysteroid (17-beta) dehydrogenase 14	gene	MP:0002687	oligozoospermia		IEA		N	RGD:5509061	20170413	MGI			
1312098	Hsd17b14	hydroxysteroid (17-beta) dehydrogenase 14	gene	MP:0008500	increased IgG2a level		IEA		N	RGD:5509061	20170413	MGI			
1312098	Hsd17b14	hydroxysteroid (17-beta) dehydrogenase 14	gene	MP:0010166	increased response to stress-induced hyperthermia		IEA		N	RGD:5509061	20170413	MGI			
1312098	Hsd17b14	hydroxysteroid (17-beta) dehydrogenase 14	gene	MP:0013600	testis degeneration		IEA		N	RGD:5509061	20170413	MGI			
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109424
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109424
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109424
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109424
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109424
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109424
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109424
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109424
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0009428	decreased tibialis anterior weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109424
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068590
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250403	MGI			PMID:12391329
1312104	Mtm1	X-linked myotubular myopathy gene 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:23109424
1312106	Ago4	argonaute RISC catalytic subunit 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863743
1312106	Ago4	argonaute RISC catalytic subunit 4	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863743
1312106	Ago4	argonaute RISC catalytic subunit 4	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863743
1312106	Ago4	argonaute RISC catalytic subunit 4	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863743
1312106	Ago4	argonaute RISC catalytic subunit 4	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863743
1312106	Ago4	argonaute RISC catalytic subunit 4	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:22863743
1312115	Lpin2	lipin 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1312115	Lpin2	lipin 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20160421	MGI			
1312115	Lpin2	lipin 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1312115	Lpin2	lipin 2	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1312115	Lpin2	lipin 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210520	MGI			
1312115	Lpin2	lipin 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20160811	MGI			
1312115	Lpin2	lipin 2	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1312115	Lpin2	lipin 2	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1312115	Lpin2	lipin 2	gene	MP:0014967	increased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22908270
1312117	Snapc2	small nuclear RNA activating complex, polypeptide 2	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20240926	MGI			
1312117	Snapc2	small nuclear RNA activating complex, polypeptide 2	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191205	MGI			
1312117	Snapc2	small nuclear RNA activating complex, polypeptide 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20191205	MGI			
1312117	Snapc2	small nuclear RNA activating complex, polypeptide 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312117	Snapc2	small nuclear RNA activating complex, polypeptide 2	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20191205	MGI			
1312117	Snapc2	small nuclear RNA activating complex, polypeptide 2	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20191205	MGI			
1312117	Snapc2	small nuclear RNA activating complex, polypeptide 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312118	Rap1gap2	RAP1 GTPase activating protein 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1312118	Rap1gap2	RAP1 GTPase activating protein 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20201022	MGI			
1312118	Rap1gap2	RAP1 GTPase activating protein 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20181227	MGI			
1312118	Rap1gap2	RAP1 GTPase activating protein 2	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1312118	Rap1gap2	RAP1 GTPase activating protein 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1312118	Rap1gap2	RAP1 GTPase activating protein 2	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20181227	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220519	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20260402	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20220519	MGI			
1312120	Art1	ADP-ribosyltransferase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20241121	MGI			
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20241121	MGI			
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0005661	decreased circulating adrenaline level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0009138	increased brown fat lipid droplet number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0012575	increased noradrenaline level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0020103	decreased hepatic glucose production		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0020426	abnormal beige fat cell physiology		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0020867	increased lipogenesis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0030020	decreased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0030761	increased adrenaline level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29378832
1312121	C2cd5	C2 calcium-dependent domain containing 5	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:29378832
1312124	Cog1	component of oligomeric golgi complex 1	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1312124	Cog1	component of oligomeric golgi complex 1	gene	MP:0002718	abnormal inner cell mass morphology		IEA		N	RGD:5509061	20241010	MGI			
1312124	Cog1	component of oligomeric golgi complex 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1312124	Cog1	component of oligomeric golgi complex 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1312126	Tmem268	transmembrane protein 268	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0002467	impaired neutrophil phagocytosis		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0012440	abnormal neutrophil cell number		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0012441	abnormal monocyte cell number		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0014902	increased circulating CCL2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:38730209
1312126	Tmem268	transmembrane protein 268	gene	MP:0020212	impaired leukocyte migration		IAGP		N	RGD:5509061	20240822	MGI			PMID:38730209
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312127	Drc2	dynein regulatory complex subunit 2	gene	MP:0013907	abnormal cerebrospinal fluid flow		IAGP		N	RGD:5509061	20240307	MGI			PMID:35844805
1312129	Ndufa7	NADH:ubiquinone oxidoreductase subunit A7	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20230601	MGI			
1312129	Ndufa7	NADH:ubiquinone oxidoreductase subunit A7	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20230601	MGI			
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20210128	MGI			
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180412	MGI			PMID:27532055
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210128	MGI			
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20180412	MGI			PMID:27532055
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20180412	MGI			PMID:27532055
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0003929	decreased heart rate variability		IAGP		N	RGD:5509061	20180412	MGI			PMID:27532055
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20180412	MGI			PMID:27532055
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180412	MGI			PMID:27532055
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312132	Polrmt	polymerase (RNA) mitochondrial (DNA directed)	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20180412	MGI			PMID:27532055
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19752223
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312136	Crtam	cytotoxic and regulatory T cell molecule	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329370
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134350
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134350
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0008510	absent retina ganglion layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134350
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312138	Nrf1	nuclear respiratory factor 1	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20200116	MGI			PMID:30333037
1312143	Agr2	anterior gradient 2	gene	MP:0000324	increased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359471
1312143	Agr2	anterior gradient 2	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20231228	MGI			PMID:25666625
1312143	Agr2	anterior gradient 2	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20025862
1312143	Agr2	anterior gradient 2	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359471
1312143	Agr2	anterior gradient 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359471
1312143	Agr2	anterior gradient 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20231228	MGI			PMID:25666625
1312143	Agr2	anterior gradient 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20025862
1312143	Agr2	anterior gradient 2	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20025862
1312143	Agr2	anterior gradient 2	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20025862
1312143	Agr2	anterior gradient 2	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20025862
1312143	Agr2	anterior gradient 2	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359471
1312143	Agr2	anterior gradient 2	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20025862
1312143	Agr2	anterior gradient 2	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20025862
1312143	Agr2	anterior gradient 2	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20025862
1312143	Agr2	anterior gradient 2	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0010799	stomach mucosa hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0010803	abnormal stomach enteroendocrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209296
1312143	Agr2	anterior gradient 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231228	MGI			PMID:25666625
1312143	Agr2	anterior gradient 2	gene	MP:0013485	increased Paneth cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:20025862
1312144	Tmem216	transmembrane protein 216	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0001785	edema		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0009744	postaxial polydactyly		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0011065	abnormal kidney epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1312144	Tmem216	transmembrane protein 216	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312144	Tmem216	transmembrane protein 216	gene	MP:0020383	decreased kidney epithelial cell primary cilium length		IAGP		N	RGD:5509061	20240328	MGI			PMID:38261656
1312145	Tecrl	trans-2,3-enoyl-CoA reductase-like	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20240523	MGI			
1312145	Tecrl	trans-2,3-enoyl-CoA reductase-like	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20240822	MGI			PMID:35577932
1312145	Tecrl	trans-2,3-enoyl-CoA reductase-like	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20240822	MGI			PMID:35577932
1312145	Tecrl	trans-2,3-enoyl-CoA reductase-like	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20240822	MGI			PMID:35577932
1312145	Tecrl	trans-2,3-enoyl-CoA reductase-like	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20240822	MGI			PMID:35577932
1312145	Tecrl	trans-2,3-enoyl-CoA reductase-like	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240822	MGI			PMID:35577932
1312145	Tecrl	trans-2,3-enoyl-CoA reductase-like	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:35577932
1312145	Tecrl	trans-2,3-enoyl-CoA reductase-like	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240822	MGI			PMID:35577932
1312147	Actr6	ARP6 actin-related protein 6	gene	MP:0003443	increased circulating glycerol level		IEA		N	RGD:5509061	20211021	MGI			
1312147	Actr6	ARP6 actin-related protein 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312149	Atg14	autophagy related 14	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24185898
1312149	Atg14	autophagy related 14	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1312149	Atg14	autophagy related 14	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1312149	Atg14	autophagy related 14	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1312149	Atg14	autophagy related 14	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1312149	Atg14	autophagy related 14	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1312149	Atg14	autophagy related 14	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1312149	Atg14	autophagy related 14	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20200514	MGI			
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301621
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301621
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20200514	MGI			
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572660
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301621
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20201022	MGI			
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301621
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301621
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301621
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20200514	MGI			
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20211021	MGI			
1312153	Rasgrp3	RAS, guanyl releasing protein 3	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20250508	MGI			
1312155	Epha6	Eph receptor A6	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1312155	Epha6	Eph receptor A6	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210128	MGI			
1312155	Epha6	Eph receptor A6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20170105	MGI			
1312155	Epha6	Eph receptor A6	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18450376
1312155	Epha6	Eph receptor A6	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18450376
1312155	Epha6	Eph receptor A6	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18450376
1312155	Epha6	Eph receptor A6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20170105	MGI			
1312155	Epha6	Eph receptor A6	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20170105	MGI			
1312155	Epha6	Eph receptor A6	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1312155	Epha6	Eph receptor A6	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20170105	MGI			
1312155	Epha6	Eph receptor A6	gene	MP:0020340	abnormal inhibitory learning		IAGP		N	RGD:5509061	20160915	MGI			PMID:18450376
1312157	Clybl	citrate lyase beta like	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1312159	Nop2	NOP2 nucleolar protein	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160421	MGI			PMID:18405070
1312160	Med12l	mediator complex subunit 12-like	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20201022	MGI			
1312160	Med12l	mediator complex subunit 12-like	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1312160	Med12l	mediator complex subunit 12-like	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1312160	Med12l	mediator complex subunit 12-like	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1312160	Med12l	mediator complex subunit 12-like	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1312162	Kdelr2	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 2	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1312162	Kdelr2	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 2	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20200402	MGI			
1312162	Kdelr2	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20190502	MGI			
1312162	Kdelr2	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160804	MGI			
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1312164	Ago1	argonaute RISC catalytic subunit 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312165	Rabgap1l	RAB GTPase activating protein 1-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:10585558
1312167	BC034090	cDNA sequence BC034090	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1312169	Mettl28	methyltransferase like 28	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1312169	Mettl28	methyltransferase like 28	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1312169	Mettl28	methyltransferase like 28	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20260402	MGI			
1312169	Mettl28	methyltransferase like 28	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1312169	Mettl28	methyltransferase like 28	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20260402	MGI			
1312169	Mettl28	methyltransferase like 28	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1312171	Map3k6	mitogen-activated protein kinase kinase kinase 6	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19214184
1312171	Map3k6	mitogen-activated protein kinase kinase kinase 6	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19214184
1312171	Map3k6	mitogen-activated protein kinase kinase kinase 6	gene	MP:0009581	decreased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19214184
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002144	abnormal B cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0002981	increased liver weight		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20231207	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20181011	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20181011	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008082	increased single-positive T cell number		IEA		N	RGD:5509061	20181011	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008205	absent B-2 B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22709692
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0009332	abnormal splenocyte morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010294	increased kidney tumor incidence		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22608497
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010511	shortened PR interval		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010574	dilated aorta		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010895	increased lung compliance		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0010936	decreased airway resistance		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0011045	decreased lung elastance		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0011048	decreased lung tissue damping		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0011951	increased cardiac stroke volume		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0013519	decreased CD4-positive NK T cell number		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0013522	decreased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0013763	increased T-helper cell number		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20250508	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27303042
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20240523	MGI			
1312177	Fnip1	folliculin interacting protein 1	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:27303042
1312181	Socs6	suppressor of cytokine signaling 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052866
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20150305	MGI			
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008211	decreased mature B cell number		IEA		N	RGD:5509061	20141003	MGI			
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015635
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934568
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20150305	MGI			
1312183	Traf3	TNF receptor-associated factor 3	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20141003	MGI			
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360997
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360997
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780988
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780988
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360997
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360997
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780988
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780988
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780988
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277503
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360997
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:17409257
1312189	Sema4a	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:23360997
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9823897
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531011
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20250508	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9823897
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20250508	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IEA		N	RGD:5509061	20111116	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716994
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20250508	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040211
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9823897
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9823897
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9823897
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9823897
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002491	decreased IgD level		IEA		N	RGD:5509061	20190110	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531011
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040211
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9889105
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040211
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20250508	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531011
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713479
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854157
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716994
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9823897
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713479
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854157
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713479
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133803
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20250508	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004941	abnormal regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716994
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716994
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9823897
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716994
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20190110	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190110	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854157
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0009314	increased colon adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133615
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190110	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190110	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040211
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531011
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9889105
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531011
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9823897
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10911993
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:10716994
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0013182	increased spinal cord apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:10716994
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190110	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0013763	increased T-helper cell number		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20260402	MGI			
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:17554302
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:19171781
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:26290337
1312195	Lig4	ligase IV, DNA, ATP-dependent	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20190110	MGI			
1312199	Stim2	stromal interaction molecule 2	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201231	MGI			
1312199	Stim2	stromal interaction molecule 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1312199	Stim2	stromal interaction molecule 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843959
1312199	Stim2	stromal interaction molecule 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1312199	Stim2	stromal interaction molecule 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843959
1312199	Stim2	stromal interaction molecule 2	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843959
1312199	Stim2	stromal interaction molecule 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1312199	Stim2	stromal interaction molecule 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1312199	Stim2	stromal interaction molecule 2	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843959
1312199	Stim2	stromal interaction molecule 2	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843959
1312199	Stim2	stromal interaction molecule 2	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843959
1312199	Stim2	stromal interaction molecule 2	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008407	decreased cellular sensitivity to hydrogen peroxide		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746875
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1312199	Stim2	stromal interaction molecule 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20181227	MGI			
1312199	Stim2	stromal interaction molecule 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843959
1312199	Stim2	stromal interaction molecule 2	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:21530328
1312201	Foxd2	forkhead box D2	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10648626
1312201	Foxd2	forkhead box D2	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:10648626
1312201	Foxd2	forkhead box D2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1312201	Foxd2	forkhead box D2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1312201	Foxd2	forkhead box D2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1312201	Foxd2	forkhead box D2	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20260402	MGI			
1312201	Foxd2	forkhead box D2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1312201	Foxd2	forkhead box D2	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20260402	MGI			
1312201	Foxd2	forkhead box D2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10648626
1312201	Foxd2	forkhead box D2	gene	MP:0002990	short ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:10648626
1312201	Foxd2	forkhead box D2	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1312201	Foxd2	forkhead box D2	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20241121	MGI			
1312201	Foxd2	forkhead box D2	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1312201	Foxd2	forkhead box D2	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20241121	MGI			
1312202	Aste1	asteroid homolog 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1312202	Aste1	asteroid homolog 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20160804	MGI			
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0002931	glutaricadicuria		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0004019	abnormal vitamin homeostasis		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0005400	abnormal vitamin level		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0005400	abnormal vitamin level		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0013754	abnormal ocular surface morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:26660539
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0014174	decreased fatty acid beta-oxidation		IAGP		N	RGD:5509061	20161222	MGI			PMID:27272163
1312204	Slc52a3	solute carrier protein family 52, member 3	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:26660539
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260702	MGI			PMID:41832173
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20190502	MGI			
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20260702	MGI			PMID:41832173
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20210513	MGI			PMID:33526923
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20210513	MGI			PMID:33526923
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20210513	MGI			PMID:33526923
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20260702	MGI			PMID:41832173
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20260702	MGI			PMID:41832173
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260702	MGI			PMID:41832173
1312207	Dis3	DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312209	Snx6	sorting nexin 6	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1312209	Snx6	sorting nexin 6	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1312209	Snx6	sorting nexin 6	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1312209	Snx6	sorting nexin 6	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20191114	MGI			PMID:28134614
1312209	Snx6	sorting nexin 6	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20191114	MGI			PMID:28134614
1312209	Snx6	sorting nexin 6	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20191114	MGI			PMID:28134614
1312209	Snx6	sorting nexin 6	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28134614
1312209	Snx6	sorting nexin 6	gene	MP:0020360	abnormal asymmetric synapse morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28134614
1312209	Snx6	sorting nexin 6	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20191114	MGI			PMID:28134614
1312209	Snx6	sorting nexin 6	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20260402	MGI			
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201022	MGI			
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004408	decreased cochlear hair cell number		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004528	fused outer hair cell stereocilia		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004533	fused inner hair cell stereocilia		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0010723	paternal effect		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20210506	MGI			PMID:29293958
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312212	Cdc14a	CDC14 cell division cycle 14A	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210506	MGI			PMID:32679235
1312215	Ppp1r13b	protein phosphatase 1, regulatory subunit 13B	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18304521
1312215	Ppp1r13b	protein phosphatase 1, regulatory subunit 13B	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18304521
1312215	Ppp1r13b	protein phosphatase 1, regulatory subunit 13B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15090446
1312215	Ppp1r13b	protein phosphatase 1, regulatory subunit 13B	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18304521
1312215	Ppp1r13b	protein phosphatase 1, regulatory subunit 13B	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18304521
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312219	Mad1l1	MAD1 mitotic arrest deficient 1-like 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22915103
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22915103
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22915103
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22915103
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22915103
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224267
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22915103
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20220519	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20210128	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20220519	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20210520	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22915103
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22915103
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0010205	abnormal oligodendrocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22915103
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224267
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489520
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20190502	MGI			
1312225	Tenm4	teneurin transmembrane protein 4	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:28453519
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20180201	MGI			PMID:28453519
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:28453519
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210520	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24270516
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20221215	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210826	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:28453519
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:28453519
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24270516
1312227	Arhgef2	Rho/Rac guanine nucleotide exchange factor 2	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:24270516
1312229	Ccl27a	C-C motif chemokine ligand 27A	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1312229	Ccl27a	C-C motif chemokine ligand 27A	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1312229	Ccl27a	C-C motif chemokine ligand 27A	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1312229	Ccl27a	C-C motif chemokine ligand 27A	gene	MP:0009080	uterus inflammation		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1312229	Ccl27a	C-C motif chemokine ligand 27A	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1312229	Ccl27a	C-C motif chemokine ligand 27A	gene	MP:0012572	increased susceptibility to chemically induced skin inflammation		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1312229	Ccl27a	C-C motif chemokine ligand 27A	gene	MP:0020212	impaired leukocyte migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1312231	Serpinb13	serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 13	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1312233	Pla2g12a	phospholipase A2, group XIIA	gene	MP:0020099	increased susceptibility to diet-induced aortic fatty streak lesions		IAGP		N	RGD:5509061	20200820	MGI			PMID:28917158
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0011282	increased podocyte apoptosis		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0011293	dilated nephron		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0011498	abnormal glomerular capsule parietal layer morphology		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312235	Tnfaip2	tumor necrosis factor, alpha-induced protein 2	gene	MP:0011863	abnormal podocyte physiology		IAGP		N	RGD:5509061	20231221	MGI			PMID:33722931
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0004962	decreased prostate gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312241	Paip2	polyadenylate-binding protein-interacting protein 2	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1312245	Blmh	bleomycin hydrolase	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10200322
1312245	Blmh	bleomycin hydrolase	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10200322
1312245	Blmh	bleomycin hydrolase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10200322
1312245	Blmh	bleomycin hydrolase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10200322
1312245	Blmh	bleomycin hydrolase	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10200322
1312245	Blmh	bleomycin hydrolase	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:10200322
1312245	Blmh	bleomycin hydrolase	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10200322
1312245	Blmh	bleomycin hydrolase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10200322
1312247	Ccndbp1	cyclin D-type binding-protein 1	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17256742
1312247	Ccndbp1	cyclin D-type binding-protein 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17256742
1312247	Ccndbp1	cyclin D-type binding-protein 1	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17256742
1312247	Ccndbp1	cyclin D-type binding-protein 1	gene	MP:0031324	delayed liver regeneration		IAGP		N	RGD:5509061	20220106	MGI			PMID:17256742
1312250	Snapc1	small nuclear RNA activating complex, polypeptide 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1312250	Snapc1	small nuclear RNA activating complex, polypeptide 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1312250	Snapc1	small nuclear RNA activating complex, polypeptide 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312250	Snapc1	small nuclear RNA activating complex, polypeptide 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312250	Snapc1	small nuclear RNA activating complex, polypeptide 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1312253	Oxct1	3-oxoacid CoA transferase 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209089
1312253	Oxct1	3-oxoacid CoA transferase 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209089
1312253	Oxct1	3-oxoacid CoA transferase 1	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209089
1312253	Oxct1	3-oxoacid CoA transferase 1	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209089
1312253	Oxct1	3-oxoacid CoA transferase 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209089
1312253	Oxct1	3-oxoacid CoA transferase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209089
1312253	Oxct1	3-oxoacid CoA transferase 1	gene	MP:0013404	decreased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:21209089
1312253	Oxct1	3-oxoacid CoA transferase 1	gene	MP:0014814	increased brain glucose metabolism		IAGP		N	RGD:5509061	20251204	MGI			PMID:21209089
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658952
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658952
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658952
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000447	flattened snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001142	abnormal vagina orifice morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170314	MGI			PMID:27264173
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20170314	MGI			PMID:27264173
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20170314	MGI			PMID:27264173
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20220804	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658952
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20220804	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11375938
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658952
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20170314	MGI			PMID:27264173
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0010754	abnormal heart left ventricle pressure		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0013599	Leydig cell atrophy		IAGP		N	RGD:5509061	20220804	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:18483174
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0015070	decreased myocardial fiber length		IAGP		N	RGD:5509061	20260813	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20160428	MGI			PMID:24993042
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0030066	short face		IEA		N	RGD:5509061	20171019	MGI			
1312255	Ddr2	discoidin domain receptor family, member 2	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:18483174
1312256	Plch2	phospholipase C, eta 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060933
1312258	Tollip	toll interacting protein	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428431
1312258	Tollip	toll interacting protein	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428431
1312258	Tollip	toll interacting protein	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428431
1312260	Pank1	pantothenate kinase 1	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20260409	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:22815849
1312260	Pank1	pantothenate kinase 1	gene	MP:0014783	decreased liver enzyme/coenzyme level		IAGP		N	RGD:5509061	20260409	MGI			PMID:20559429
1312260	Pank1	pantothenate kinase 1	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:20559429
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20171026	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615710
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1312262	Gdf1	growth differentiation factor 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1312262	Gdf1	growth differentiation factor 1	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1312262	Gdf1	growth differentiation factor 1	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615710
1312262	Gdf1	growth differentiation factor 1	gene	MP:0004388	absent prechordal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0004714	truncated notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0006062	abnormal vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0006261	annular pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1312262	Gdf1	growth differentiation factor 1	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20171026	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0010335	fused first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18615710
1312262	Gdf1	growth differentiation factor 1	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1312262	Gdf1	growth differentiation factor 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700179
1312262	Gdf1	growth differentiation factor 1	gene	MP:0011255	abnormal anterior visceral endoderm cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1312262	Gdf1	growth differentiation factor 1	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1312262	Gdf1	growth differentiation factor 1	gene	MP:0012159	absent anterior visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1312262	Gdf1	growth differentiation factor 1	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1312262	Gdf1	growth differentiation factor 1	gene	MP:0030198	nasal septum hypoplasia		IAGP		N	RGD:5509061	20171012	MGI			PMID:16564040
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210520	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20220519	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20230755
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0010039	abnormal trophoblast giant cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20230755
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20230755
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20230755
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20230755
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0013415	increased myeloid cell number in bone marrow		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20150730	MGI			PMID:25678499
1312264	Chordc1	cysteine and histidine rich domain containing 1	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:25678499
1312266	Epha1	Eph receptor A1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0003537	hydrometrocolpos		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0003541	vaginal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0009087	dilated uterine horn		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312266	Epha1	Eph receptor A1	gene	MP:0009360	endometrium inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802966
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807096
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381686
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:1634998
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17197442
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000753	paralysis		IEA		N	RGD:5509061	20150312	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1634998
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000755	hindlimb paralysis		IEA		N	RGD:5509061	20150312	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381686
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17197442
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381686
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1634998
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381686
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20250206	MGI			PMID:11807096
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807096
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381686
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:1634998
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20111116	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001504	abnormal posture		IEA		N	RGD:5509061	20111116	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807096
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001525	impaired balance		IEA		N	RGD:5509061	20111116	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001851	eye inflammation		IEA		N	RGD:5509061	20150312	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1634998
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20150312	MGI			PMID:4067076
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20111116	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20111116	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381686
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:1634998
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0003314	dysmetria		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381686
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0003415	priapism		IEA		N	RGD:5509061	20150312	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0004631	abnormal auditory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11528393
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11528393
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15381686
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0004813	absent linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0004814	reduced linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17197442
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807096
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17197442
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0006325	impaired hearing		IEA		N	RGD:5509061	20111116	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0009434	paraparesis		IEA		N	RGD:5509061	20111116	MGI			
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:11528393
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11528393
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0014740	increased auditory brainstem response wave peak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:16235133
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:11528393
1312270	Sptbn4	spectrin beta, non-erythrocytic 4	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:16235133
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095744
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16603466
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20190131	MGI			PMID:19815523
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16603466
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20160407	MGI			PMID:25712131
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20190131	MGI			PMID:19815523
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0004213	abnormal umami taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342734
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095744
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0005423	abnormal somatic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342734
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367617
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20190314	MGI			PMID:19815523
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095744
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0006243	impaired pupillary reflex		IAGP		N	RGD:5509061	20230713	MGI			PMID:12808468
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367617
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095744
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095744
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221340
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20160407	MGI			PMID:25712131
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:11095744
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:12808468
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20171012	MGI			PMID:12808468
1312272	Gnat1	G protein subunit alpha transducin 1	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:11095744
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0006083	abnormal blood vessel elastic tissue morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312274	Poglut2	protein O-glucosyltransferase 2	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20240801	MGI			PMID:38844137
1312277	Eif1ad	eukaryotic translation initiation factor 1A domain containing	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1312277	Eif1ad	eukaryotic translation initiation factor 1A domain containing	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1312277	Eif1ad	eukaryotic translation initiation factor 1A domain containing	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312277	Eif1ad	eukaryotic translation initiation factor 1A domain containing	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1312277	Eif1ad	eukaryotic translation initiation factor 1A domain containing	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312277	Eif1ad	eukaryotic translation initiation factor 1A domain containing	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1312278	Alkbh8	alkB homolog 8, tRNA methyltransferase	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20260402	MGI			
1312278	Alkbh8	alkB homolog 8, tRNA methyltransferase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1312278	Alkbh8	alkB homolog 8, tRNA methyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20123966
1312278	Alkbh8	alkB homolog 8, tRNA methyltransferase	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1312278	Alkbh8	alkB homolog 8, tRNA methyltransferase	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1312278	Alkbh8	alkB homolog 8, tRNA methyltransferase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1312281	Tubgcp5	tubulin, gamma complex component 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1312282	Eml4	echinoderm microtubule associated protein like 4	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1312282	Eml4	echinoderm microtubule associated protein like 4	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1312282	Eml4	echinoderm microtubule associated protein like 4	gene	MP:0003896	prolonged PR interval		IEA		N	RGD:5509061	20240523	MGI			
1312282	Eml4	echinoderm microtubule associated protein like 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210826	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20200514	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20241121	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20200514	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20200514	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20241121	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20220811	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20210826	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200514	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1312284	Rabgap1	RAB GTPase activating protein 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1312288	5031439G07Rik	RIKEN cDNA 5031439G07 gene	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1312291	Txndc15	thioredoxin domain containing 15	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20260423	MGI			PMID:41518077
1312291	Txndc15	thioredoxin domain containing 15	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20260423	MGI			PMID:41518077
1312291	Txndc15	thioredoxin domain containing 15	gene	MP:0009744	postaxial polydactyly		IAGP		N	RGD:5509061	20260423	MGI			PMID:41518077
1312291	Txndc15	thioredoxin domain containing 15	gene	MP:0010912	herniated liver		IAGP		N	RGD:5509061	20260423	MGI			PMID:41518077
1312291	Txndc15	thioredoxin domain containing 15	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20260423	MGI			PMID:41518077
1312291	Txndc15	thioredoxin domain containing 15	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20260423	MGI			PMID:41518077
1312293	Actl7a	actin-like 7a	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20211209	MGI			PMID:32923619
1312293	Actl7a	actin-like 7a	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20211209	MGI			PMID:32923619
1312293	Actl7a	actin-like 7a	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:32923619
1312293	Actl7a	actin-like 7a	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20211209	MGI			PMID:32923619
1312296	Naxe	NAD(P)HX epimerase	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1312296	Naxe	NAD(P)HX epimerase	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20190228	MGI			PMID:28325782
1312296	Naxe	NAD(P)HX epimerase	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20241121	MGI			
1312296	Naxe	NAD(P)HX epimerase	gene	MP:0003711	pathological neovascularization		IAGP		N	RGD:5509061	20190228	MGI			PMID:28325782
1312296	Naxe	NAD(P)HX epimerase	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1312296	Naxe	NAD(P)HX epimerase	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20190228	MGI			PMID:28325782
1312296	Naxe	NAD(P)HX epimerase	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20241121	MGI			
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0000336	decreased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466727
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466727
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0000361	decreased mast cell protease storage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466726
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0000361	decreased mast cell protease storage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466727
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0000362	decreased mast cell histamine storage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466726
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0000362	decreased mast cell histamine storage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466727
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0001347	absent lacrimal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077586
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0001347	absent lacrimal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745308
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19109198
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466726
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0005462	abnormal mast cell differentiation		IAGP		N	RGD:5509061	20150416	MGI			PMID:19109198
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466726
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10466727
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16056228
1312298	Ndst2	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	gene	MP:0013331	abnormal lacrimal gland development		IAGP		N	RGD:5509061	20141204	MGI			PMID:22745308
1312304	Tnfrsf17	tumor necrosis factor receptor superfamily, member 17	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1312304	Tnfrsf17	tumor necrosis factor receptor superfamily, member 17	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1312304	Tnfrsf17	tumor necrosis factor receptor superfamily, member 17	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14707116
1312304	Tnfrsf17	tumor necrosis factor receptor superfamily, member 17	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210826	MGI			
1312306	Rtraf	RNA transcription, translation and transport factor	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20170105	MGI			
1312306	Rtraf	RNA transcription, translation and transport factor	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1312306	Rtraf	RNA transcription, translation and transport factor	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1312306	Rtraf	RNA transcription, translation and transport factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312306	Rtraf	RNA transcription, translation and transport factor	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1312308	Tmem147	transmembrane protein 147	gene	MP:0000579	abnormal nail morphology		IEA		N	RGD:5509061	20210826	MGI			
1312308	Tmem147	transmembrane protein 147	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20210826	MGI			
1312308	Tmem147	transmembrane protein 147	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312314	Ca8	carbonic anhydrase 8	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160519	MGI			PMID:26586559
1312314	Ca8	carbonic anhydrase 8	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:26586559
1312314	Ca8	carbonic anhydrase 8	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20160519	MGI			PMID:26586559
1312314	Ca8	carbonic anhydrase 8	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118194
1312314	Ca8	carbonic anhydrase 8	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160519	MGI			PMID:26586559
1312314	Ca8	carbonic anhydrase 8	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
1312314	Ca8	carbonic anhydrase 8	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20160519	MGI			PMID:26586559
1312314	Ca8	carbonic anhydrase 8	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20160519	MGI			PMID:26586559
1312314	Ca8	carbonic anhydrase 8	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20141003	MGI			
1312314	Ca8	carbonic anhydrase 8	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20160519	MGI			PMID:26586559
1312319	Jcad	junctional cadherin 5 associated	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191031	MGI			PMID:28705794
1312319	Jcad	junctional cadherin 5 associated	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1312319	Jcad	junctional cadherin 5 associated	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230601	MGI			
1312319	Jcad	junctional cadherin 5 associated	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20191031	MGI			PMID:28705794
1312319	Jcad	junctional cadherin 5 associated	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
1312319	Jcad	junctional cadherin 5 associated	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20191031	MGI			PMID:28705794
1312319	Jcad	junctional cadherin 5 associated	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20191031	MGI			PMID:28705794
1312319	Jcad	junctional cadherin 5 associated	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1312319	Jcad	junctional cadherin 5 associated	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1312321	Eral1	Era like 12S mitochondrial rRNA chaperone 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312321	Eral1	Era like 12S mitochondrial rRNA chaperone 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312325	Cxcl17	C-X-C motif chemokine ligand 17	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1312325	Cxcl17	C-X-C motif chemokine ligand 17	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20170105	MGI			
1312325	Cxcl17	C-X-C motif chemokine ligand 17	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201231	MGI			
1312325	Cxcl17	C-X-C motif chemokine ligand 17	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1312325	Cxcl17	C-X-C motif chemokine ligand 17	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1312325	Cxcl17	C-X-C motif chemokine ligand 17	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1312325	Cxcl17	C-X-C motif chemokine ligand 17	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210520	MGI			
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20260402	MGI			
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20260402	MGI			
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20201022	MGI			PMID:26062998
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20201022	MGI			PMID:26062998
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0008141	decreased small intestinal microvillus size		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0014262	increased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:31296356
1312329	Ikzf4	IKAROS family zinc finger 4	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1312332	Cadm4	cell adhesion molecule 4	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825401
1312332	Cadm4	cell adhesion molecule 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825401
1312332	Cadm4	cell adhesion molecule 4	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825401
1312332	Cadm4	cell adhesion molecule 4	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825401
1312332	Cadm4	cell adhesion molecule 4	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825401
1312332	Cadm4	cell adhesion molecule 4	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825401
1312332	Cadm4	cell adhesion molecule 4	gene	MP:0010734	abnormal paranode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825401
1312333	Them4	thioesterase superfamily member 4	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:19421406
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470461
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470461
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470461
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470461
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470461
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1312335	Sox21	SRY (sex determining region Y)-box 21	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1312337	Dnajb1	DnaJ heat shock protein family (Hsp40) member B1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17050614
1312340	4933427D14Rik	RIKEN cDNA 4933427D14 gene	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20241212	MGI			PMID:34241634
1312340	4933427D14Rik	RIKEN cDNA 4933427D14 gene	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191128	MGI			
1312340	4933427D14Rik	RIKEN cDNA 4933427D14 gene	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20191128	MGI			
1312340	4933427D14Rik	RIKEN cDNA 4933427D14 gene	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20241212	MGI			PMID:34241634
1312340	4933427D14Rik	RIKEN cDNA 4933427D14 gene	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20191128	MGI			
1312340	4933427D14Rik	RIKEN cDNA 4933427D14 gene	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:34241634
1312340	4933427D14Rik	RIKEN cDNA 4933427D14 gene	gene	MP:0013214	decreased embryonic neuroepithelium primary cilium number		IAGP		N	RGD:5509061	20241212	MGI			PMID:34241634
1312340	4933427D14Rik	RIKEN cDNA 4933427D14 gene	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20241212	MGI			PMID:34241634
1312342	Sfn	stratifin	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:24075906
1312342	Sfn	stratifin	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439433
1312342	Sfn	stratifin	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0000384	distorted hair follicle pattern		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0000416	sparse hair		IEA		N	RGD:5509061	20111116	MGI			
1312342	Sfn	stratifin	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0000447	flattened snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:6174530
1312342	Sfn	stratifin	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6174530
1312342	Sfn	stratifin	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24075906
1312342	Sfn	stratifin	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6174530
1312342	Sfn	stratifin	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6174530
1312342	Sfn	stratifin	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24075906
1312342	Sfn	stratifin	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6174530
1312342	Sfn	stratifin	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6374282
1312342	Sfn	stratifin	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:2989601
1312342	Sfn	stratifin	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0002234	abnormal pharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0002251	abnormal nasopharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:24075906
1312342	Sfn	stratifin	gene	MP:0003130	anal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0003160	abnormal esophagus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0003315	abnormal perineum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439433
1312342	Sfn	stratifin	gene	MP:0003671	abnormal eyelid aperture		IAGP		N	RGD:5509061	20141003	MGI			PMID:6374282
1312342	Sfn	stratifin	gene	MP:0003775	thin lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:2989601
1312342	Sfn	stratifin	gene	MP:0004575	small limb buds		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0004576	abnormal embryonic autopod plate morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0005155	herniated intestine		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0009263	abnormal eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:6374282
1312342	Sfn	stratifin	gene	MP:0009474	thick epidermis stratum spinosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439433
1312342	Sfn	stratifin	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439433
1312342	Sfn	stratifin	gene	MP:0009553	fused lips		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0009553	fused lips		IAGP		N	RGD:5509061	20230601	MGI			PMID:6746880
1312342	Sfn	stratifin	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1312342	Sfn	stratifin	gene	MP:0009576	oral atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24075906
1312342	Sfn	stratifin	gene	MP:0009576	oral atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0009884	palatal shelf fusion with tongue or mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24075906
1312342	Sfn	stratifin	gene	MP:0012175	flat face		IAGP		N	RGD:5509061	20171019	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0013789	small external nares		IAGP		N	RGD:5509061	20150611	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0013789	small external nares		IAGP		N	RGD:5509061	20150611	MGI			PMID:6643653
1312342	Sfn	stratifin	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20170914	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:21205887
1312342	Sfn	stratifin	gene	MP:0021208	median cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:479550
1312342	Sfn	stratifin	gene	MP:0030179	abnormal oral epithelium morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:16239341
1312342	Sfn	stratifin	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:21205887
1312346	Styx	serine/threonine/tyrosine interaction protein	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11842224
1312346	Styx	serine/threonine/tyrosine interaction protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11842224
1312346	Styx	serine/threonine/tyrosine interaction protein	gene	MP:0002208	abnormal germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11842224
1312346	Styx	serine/threonine/tyrosine interaction protein	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11842224
1312346	Styx	serine/threonine/tyrosine interaction protein	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11842224
1312346	Styx	serine/threonine/tyrosine interaction protein	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11842224
1312346	Styx	serine/threonine/tyrosine interaction protein	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11842224
1312349	Elmo3	engulfment and cell motility 3	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20170105	MGI			
1312349	Elmo3	engulfment and cell motility 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534472
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534472
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534472
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534472
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534472
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534472
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534472
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0008878	abnormal DNA methylation during gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534472
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:20547853
1312350	Mov10l1	Mov10 like RISC complex RNA helicase 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:20547853
1312354	Zfr2	zinc finger RNA binding protein 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240627	MGI			PMID:36440598
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:36440598
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20240627	MGI			PMID:36440598
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:36440598
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314518
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20240627	MGI			PMID:36440598
1312356	Ube4b	ubiquitination factor E4B	gene	MP:0021090	abnormal dendrite arborization pattern		IAGP		N	RGD:5509061	20240627	MGI			PMID:36440598
1312358	Exosc3	exosome component 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1312358	Exosc3	exosome component 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1312358	Exosc3	exosome component 3	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20210128	MGI			
1312358	Exosc3	exosome component 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1312358	Exosc3	exosome component 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312358	Exosc3	exosome component 3	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1312358	Exosc3	exosome component 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1312358	Exosc3	exosome component 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220519	MGI			
1312362	Rab37	RAB37, member RAS oncogene family	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20230406	MGI			PMID:36109708
1312362	Rab37	RAB37, member RAS oncogene family	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20230406	MGI			PMID:36109708
1312366	Stx11	syntaxin 11	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1312366	Stx11	syntaxin 11	gene	MP:0002421	abnormal cell-mediated immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042080
1312366	Stx11	syntaxin 11	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042080
1312366	Stx11	syntaxin 11	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20201022	MGI			
1312366	Stx11	syntaxin 11	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1312366	Stx11	syntaxin 11	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042080
1312366	Stx11	syntaxin 11	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042080
1312366	Stx11	syntaxin 11	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1312366	Stx11	syntaxin 11	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042080
1312366	Stx11	syntaxin 11	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210520	MGI			
1312366	Stx11	syntaxin 11	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042080
1312366	Stx11	syntaxin 11	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042080
1312366	Stx11	syntaxin 11	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0008791	decreased NK cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1312366	Stx11	syntaxin 11	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1312366	Stx11	syntaxin 11	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23160464
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274056
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274056
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274056
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730693
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242117
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242117
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730693
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730693
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0008090	increased T-helper 2 cell number		IAGP		N	RGD:5509061	20220519	MGI			PMID:34420035
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274056
1312369	Mbd2	methyl-CpG binding domain protein 2	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20250508	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0000497	abnormal small intestine placement		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20190221	MGI			PMID:28717248
1312371	Adcy9	adenylate cyclase 9	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1312371	Adcy9	adenylate cyclase 9	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0003888	liver hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0004666	absent stapedial artery		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0005272	abnormal temporal bone morphology		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20190221	MGI			PMID:28717248
1312371	Adcy9	adenylate cyclase 9	gene	MP:0008499	increased IgG1 level		IEA		N	RGD:5509061	20111116	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0009571	abnormal right lung accessory lobe morphology		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190221	MGI			PMID:28717248
1312371	Adcy9	adenylate cyclase 9	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1312371	Adcy9	adenylate cyclase 9	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0013847	retropleural edema		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0013852	abnormal Mullerian duct topology		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0013985	abnormal umbilical vein topology		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0014003	additional anastomosis between intracranial vertebral arteries		IEA		N	RGD:5509061	20170504	MGI			
1312371	Adcy9	adenylate cyclase 9	gene	MP:0014087	retrolental blood		IEA		N	RGD:5509061	20180628	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000107	abnormal frontal bone morphology		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000116	abnormal tooth development		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000119	abnormal tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000128	growth retardation of molars		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000138	absent vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000436	abnormal head movements		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000555	absent carpal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545599
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:24203697
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20151119	MGI			PMID:25917329
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545599
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0000963	fused dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545599
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001677	absent apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20151119	MGI			PMID:25917329
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948618
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002177	abnormal outer ear morphology		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002233	abnormal nose morphology		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20151119	MGI			PMID:25917329
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002632	vestigial tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003050	abnormal sacral vertebrae morphology		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:24203697
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:24203697
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003074	absent metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003126	abnormal external female genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20151119	MGI			PMID:25917329
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003445	sirenomelia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003445	sirenomelia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003800	monodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003883	enlarged stomach		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:24203697
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004652	small caudal vertebrae		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0004830	short incisors		IEA		N	RGD:5509061	20171005	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005352	small cranium		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0008274	failure of bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0008832	hemivertebra		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0009039	absent inferior colliculus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0009127	increased brown fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0009199	abnormal external male genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0009263	abnormal eyelid fusion		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0009703	decreased birth body size		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20151119	MGI			PMID:24506864
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20151119	MGI			PMID:25917329
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0010715	retina coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0010743	delayed cranial suture closure		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545599
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545599
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20111201	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011496	abnormal head size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16126904
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0012062	small tail bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0012078	abnormal tail ring morphology		IAGP		N	RGD:5509061	20170309	MGI			PMID:5893447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0012139	increased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0012184	absent paraxial mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0012547	spina bifida cystica		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469977
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0013207	absent endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:21237142
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:11029008
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:15142971
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:15537447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:19653321
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20180125	MGI			PMID:22232553
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0030080	small lower incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:5893447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0030083	long upper incisors		IEA		N	RGD:5509061	20180125	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0030279	thin neurocranium		IEA		N	RGD:5509061	20171102	MGI			
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:5893447
1312374	Lrp6	low density lipoprotein receptor-related protein 6	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:22232553
1312376	Dqx1	DEAQ RNA-dependent ATPase	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1312376	Dqx1	DEAQ RNA-dependent ATPase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1312376	Dqx1	DEAQ RNA-dependent ATPase	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20250508	MGI			
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19014927
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20150917	MGI			PMID:18339773
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20150917	MGI			PMID:18339773
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19014927
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20150917	MGI			PMID:18339773
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18753606
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19014927
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19014927
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19014927
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19014927
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20150917	MGI			PMID:18339773
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18753606
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18753606
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19014927
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20150917	MGI			PMID:18339773
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20150917	MGI			PMID:18339773
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18753606
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19014927
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:18339773
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19014927
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:18339773
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18753606
1312378	Sohlh2	spermatogenesis and oogenesis specific basic helix-loop-helix 2	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18753606
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20240523	MGI			
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20240523	MGI			
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20240523	MGI			
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20240523	MGI			
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7641686
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7641686
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20240523	MGI			
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0004918	abnormal negative T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7641686
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7641686
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7641686
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7641686
1312381	Hcls1	hematopoietic cell specific Lyn substrate 1	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20260402	MGI			
1312383	Phlda2	pleckstrin homology like domain, family A, member 2	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
1312383	Phlda2	pleckstrin homology like domain, family A, member 2	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
1312383	Phlda2	pleckstrin homology like domain, family A, member 2	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
1312383	Phlda2	pleckstrin homology like domain, family A, member 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
1312383	Phlda2	pleckstrin homology like domain, family A, member 2	gene	MP:0012098	increased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
1312383	Phlda2	pleckstrin homology like domain, family A, member 2	gene	MP:0012108	increased trophoblast glycogen cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
1312385	Fank1	fibronectin type 3 and ankyrin repeat domains 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:31086747
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20211021	MGI			
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0003750	increased mouth tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484223
1312388	Palb2	partner and localizer of BRCA2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1312399	Ano6	anoctamin 6	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1312399	Ano6	anoctamin 6	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23021219
1312399	Ano6	anoctamin 6	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20201022	MGI			
1312399	Ano6	anoctamin 6	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23021219
1312399	Ano6	anoctamin 6	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:23021219
1312399	Ano6	anoctamin 6	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20180503	MGI			PMID:24974903
1312399	Ano6	anoctamin 6	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0010926	increased osteoid volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0010929	increased osteoid thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1312399	Ano6	anoctamin 6	gene	MP:0011954	shortened PQ interval		IEA		N	RGD:5509061	20210826	MGI			
1312399	Ano6	anoctamin 6	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0020138	delayed bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0030857	absent olecranon		IAGP		N	RGD:5509061	20181025	MGI			PMID:22936354
1312399	Ano6	anoctamin 6	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:23021219
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000624	xerostomia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002360	abnormal spleen B cell corona morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002742	enlarged submandibular lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155511
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0003746	stomatitis		IAGP		N	RGD:5509061	20170907	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155511
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155511
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008121	increased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008188	abnormal transitional stage B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008542	enlarged cervical lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155511
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155511
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155511
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008879	submandibular gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0008896	increased IgG2c level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0009521	increased submandibular gland size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22585710
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0013367	parotid gland inflammation		IAGP		N	RGD:5509061	20141225	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0013558	abnormal exocrine gland morphology		IAGP		N	RGD:5509061	20170907	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:18624351
1312404	Traf3ip2	TRAF3 interacting protein 2	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:22585710
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20250508	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230601	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20251127	MGI			PMID:33297405
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20251127	MGI			PMID:33297405
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20250508	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20251127	MGI			PMID:33297405
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0003824	decreased left ventricle developed pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0004567	decreased myocardial fiber number		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20250508	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20251127	MGI			PMID:33297405
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0009208	abnormal female genitalia morphology		IEA		N	RGD:5509061	20260402	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0009211	absent external female genitalia		IEA		N	RGD:5509061	20260402	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230601	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550297
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371351
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20150101	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20190711	MGI			PMID:29438013
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:21897366
1312408	Cnot3	CCR4-NOT transcription complex, subunit 3	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:20371351
1312411	Castor1	cytosolic arginine sensor for mTORC1 subunit 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1312412	Ccdc150	coiled-coil domain containing 150	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16708114
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0004093	diffuse Z line		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16708114
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0010393	shortened QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0010554	shortened HV interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843512
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0014731	disorganized myocardial fiber myofibrils		IAGP		N	RGD:5509061	20250911	MGI			PMID:16708114
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0014731	disorganized myocardial fiber myofibrils		IAGP		N	RGD:5509061	20250911	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0014921	decreased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0015067	increased myocardial fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0020345	abnormal myocardial fiber currents		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0020346	abnormal myocardial fiber calcium currents		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0020347	abnormal myocardial fiber sodium currents		IAGP		N	RGD:5509061	20170824	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0030566	abnormal A band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:17766470
1312414	Xirp1	xin actin-binding repeat containing 1	gene	MP:0030567	abnormal I band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:17766470
1312416	Nrip3	nuclear receptor interacting protein 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1312416	Nrip3	nuclear receptor interacting protein 3	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20260402	MGI			
1312419	Lrrc23	leucine rich repeat containing 23	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220310	MGI			PMID:34585727
1312419	Lrrc23	leucine rich repeat containing 23	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220310	MGI			PMID:34585727
1312419	Lrrc23	leucine rich repeat containing 23	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220310	MGI			PMID:34585727
1312419	Lrrc23	leucine rich repeat containing 23	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1312419	Lrrc23	leucine rich repeat containing 23	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:34585727
1312419	Lrrc23	leucine rich repeat containing 23	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220310	MGI			PMID:34585727
1312419	Lrrc23	leucine rich repeat containing 23	gene	MP:0031438	abnormal sperm radial spoke morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34585727
1312421	Spats2	spermatogenesis associated, serine-rich 2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20230119	MGI			
1312421	Spats2	spermatogenesis associated, serine-rich 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1312423	Trit1	tRNA isopentenyltransferase 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1312423	Trit1	tRNA isopentenyltransferase 1	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20240627	MGI			
1312423	Trit1	tRNA isopentenyltransferase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1312423	Trit1	tRNA isopentenyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312423	Trit1	tRNA isopentenyltransferase 1	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1312423	Trit1	tRNA isopentenyltransferase 1	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20240627	MGI			
1312423	Trit1	tRNA isopentenyltransferase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312423	Trit1	tRNA isopentenyltransferase 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000035	abnormal membranous labyrinth morphology		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1638738
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000585	kinked tail		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17019651
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1638738
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741143
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1638738
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741143
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17019651
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741143
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1638738
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741143
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1638738
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17019651
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000869	abnormal cerebellum posterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17019651
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000923	abnormal roof plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000923	abnormal roof plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14251482
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17019651
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14914015
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001395	bidirectional circling		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14914015
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17019651
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001516	abnormal motor coordination/balance		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001924	infertility		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14914015
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14251482
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002161	abnormal fertility/fecundity		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002428	abnormal semicircular canal morphology		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002671	belted		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002671	belted		IAGP		N	RGD:5509061	20141003	MGI			PMID:14914015
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002862	abnormal righting response		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:10444330
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17019651
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0003938	abnormal ear development		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0004289	abnormal bony labyrinth		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0004315	absent vestibular saccule		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0004369	absent utricle		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0004426	abnormal cochlear labyrinth morphology		IEA		N	RGD:5509061	20111215	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0004427	abnormal vestibular labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0004750	syndromic hearing loss		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:14914015
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8242357
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20211125	MGI			PMID:1638738
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006014	dilated endolymphatic sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006281	abnormal tail development		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006286	inner ear hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1638738
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:1638738
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0008307	short scala media		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21752929
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0008854	bleb		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0009393	abnormal resting posture		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0009719	reduced cerebellar foliation		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21752929
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21752929
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226461
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0012792	abnormal rhombomere 3 morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0012796	abnormal rhombomere 4 morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0012800	abnormal rhombomere 5 morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10842066
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0014365	impaired short-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:25915474
1312427	Lmx1a	LIM homeobox transcription factor 1 alpha	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25915474
1312430	Rbpjl	recombination signal binding protein for immunoglobulin kappa J region-like	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1312430	Rbpjl	recombination signal binding protein for immunoglobulin kappa J region-like	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20200402	MGI			
1312430	Rbpjl	recombination signal binding protein for immunoglobulin kappa J region-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502683
1312430	Rbpjl	recombination signal binding protein for immunoglobulin kappa J region-like	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20181227	MGI			
1312434	Lactb	lactamase, beta	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1312434	Lactb	lactamase, beta	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20181227	MGI			
1312434	Lactb	lactamase, beta	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1312434	Lactb	lactamase, beta	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20181227	MGI			
1312434	Lactb	lactamase, beta	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20190502	MGI			
1312434	Lactb	lactamase, beta	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1312434	Lactb	lactamase, beta	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20181227	MGI			
1312434	Lactb	lactamase, beta	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312434	Lactb	lactamase, beta	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20251002	MGI			PMID:39561766
1312437	Fam43a	family with sequence similarity 43, member A	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1312437	Fam43a	family with sequence similarity 43, member A	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1312442	Tmem222	transmembrane protein 222	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1312442	Tmem222	transmembrane protein 222	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1312442	Tmem222	transmembrane protein 222	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312444	Cenpb	centromere protein B	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016956
1312444	Cenpb	centromere protein B	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548711
1312444	Cenpb	centromere protein B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548711
1312444	Cenpb	centromere protein B	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9740654
1312444	Cenpb	centromere protein B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9933410
1312444	Cenpb	centromere protein B	gene	MP:0002292	abnormal gestational length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548711
1312444	Cenpb	centromere protein B	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15016956
1312444	Cenpb	centromere protein B	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312444	Cenpb	centromere protein B	gene	MP:0012008	delayed parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:10645947
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25336629
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20260402	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20250508	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20250508	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20241121	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20210826	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20211021	MGI			
1312446	Apbb1ip	amyloid beta precursor protein binding family B member 1 interacting protein	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20210826	MGI			
1312450	B3galnt1	UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 1	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463849
1312450	B3galnt1	UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1312450	B3galnt1	UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 1	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463849
1312454	Dguok	deoxyguanosine kinase	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1312454	Dguok	deoxyguanosine kinase	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20190502	MGI			
1312454	Dguok	deoxyguanosine kinase	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20190502	MGI			
1312454	Dguok	deoxyguanosine kinase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1312454	Dguok	deoxyguanosine kinase	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1312454	Dguok	deoxyguanosine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1312454	Dguok	deoxyguanosine kinase	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0005516	enhanced liver regeneration		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1312454	Dguok	deoxyguanosine kinase	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1312454	Dguok	deoxyguanosine kinase	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0012017	grizzled coat color		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0014388	decreased hepatocyte mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0014389	decreased skeletal muscle fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0014390	decreased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0014906	abnormal muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:31127938
1312454	Dguok	deoxyguanosine kinase	gene	MP:0020427	increased hepatocyte karyomegaly		IAGP		N	RGD:5509061	20201022	MGI			PMID:31127938
1312456	Gga2	golgi associated, gamma adaptin ear containing, ARF binding protein 2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1312456	Gga2	golgi associated, gamma adaptin ear containing, ARF binding protein 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1312456	Gga2	golgi associated, gamma adaptin ear containing, ARF binding protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1312456	Gga2	golgi associated, gamma adaptin ear containing, ARF binding protein 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1312456	Gga2	golgi associated, gamma adaptin ear containing, ARF binding protein 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1312458	S1pr4	sphingosine-1-phosphate receptor 4	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20686109
1312458	S1pr4	sphingosine-1-phosphate receptor 4	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20686109
1312458	S1pr4	sphingosine-1-phosphate receptor 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20111116	MGI			
1312458	S1pr4	sphingosine-1-phosphate receptor 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1312460	Frmd3	FERM domain containing 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1312460	Frmd3	FERM domain containing 3	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20220811	MGI			
1312460	Frmd3	FERM domain containing 3	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210520	MGI			
1312460	Frmd3	FERM domain containing 3	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230601	MGI			
1312460	Frmd3	FERM domain containing 3	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0009508	increased mammary gland ductal carcinoma incidence		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0010173	increased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0012075	impaired mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0013778	abnormal mammary gland myoepithelium morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0013781	abnormal mammary gland luminal epithelium morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312460	Frmd3	FERM domain containing 3	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20250130	MGI			PMID:38959315
1312463	Tll2	tolloid-like 2	gene	MP:0003397	increased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286185
1312466	Tcaf2	TRPM8 channel-associated factor 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1312466	Tcaf2	TRPM8 channel-associated factor 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1312466	Tcaf2	TRPM8 channel-associated factor 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1312466	Tcaf2	TRPM8 channel-associated factor 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1312466	Tcaf2	TRPM8 channel-associated factor 2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1312466	Tcaf2	TRPM8 channel-associated factor 2	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230601	MGI			
1312466	Tcaf2	TRPM8 channel-associated factor 2	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1312466	Tcaf2	TRPM8 channel-associated factor 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1312466	Tcaf2	TRPM8 channel-associated factor 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1312472	Trmt9b	tRNA methyltransferase 9B	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20200514	MGI			
1312474	Tmc4	transmembrane channel-like gene family 4	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1312474	Tmc4	transmembrane channel-like gene family 4	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1312474	Tmc4	transmembrane channel-like gene family 4	gene	MP:0001985	abnormal gustatory system physiology		IAGP		N	RGD:5509061	20220421	MGI			PMID:34429071
1312474	Tmc4	transmembrane channel-like gene family 4	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1312474	Tmc4	transmembrane channel-like gene family 4	gene	MP:0004212	abnormal salty taste sensitivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:34429071
1312474	Tmc4	transmembrane channel-like gene family 4	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20240523	MGI			
1312485	Cdc23	CDC23 cell division cycle 23	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1312485	Cdc23	CDC23 cell division cycle 23	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20240314	MGI			PMID:37768355
1312485	Cdc23	CDC23 cell division cycle 23	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1312485	Cdc23	CDC23 cell division cycle 23	gene	MP:0010767	abnormal female meiosis I arrest		IAGP		N	RGD:5509061	20240314	MGI			PMID:37768355
1312485	Cdc23	CDC23 cell division cycle 23	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312485	Cdc23	CDC23 cell division cycle 23	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312486	Palld	palladin, cytoskeletal associated protein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15950489
1312486	Palld	palladin, cytoskeletal associated protein	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15950489
1312486	Palld	palladin, cytoskeletal associated protein	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15950489
1312486	Palld	palladin, cytoskeletal associated protein	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15950489
1312486	Palld	palladin, cytoskeletal associated protein	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:15950489
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:22402282
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22402282
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22402282
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0002078	abnormal glucose homeostasis		IEA		N	RGD:5509061	20141003	MGI			
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22402282
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201231	MGI			
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20160804	MGI			
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0005102	abnormal iris pigmentation		IEA		N	RGD:5509061	20141003	MGI			
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0005316	abnormal response to tactile stimuli		IEA		N	RGD:5509061	20141003	MGI			
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22402282
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22241836
1312489	Kdm8	lysine (K)-specific demethylase 8	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1312491	Timcc	TIM double twin CX3C motif chaperone	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20240215	MGI			PMID:37461313
1312496	Med13	mediator complex subunit 13	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20260402	MGI			PMID:40989238
1312496	Med13	mediator complex subunit 13	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260402	MGI			PMID:40989238
1312496	Med13	mediator complex subunit 13	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20260402	MGI			PMID:40989238
1312496	Med13	mediator complex subunit 13	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20260402	MGI			PMID:40989238
1312496	Med13	mediator complex subunit 13	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20260402	MGI			PMID:40989238
1312496	Med13	mediator complex subunit 13	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20260402	MGI			PMID:40989238
1312496	Med13	mediator complex subunit 13	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20260402	MGI			PMID:40989238
1312496	Med13	mediator complex subunit 13	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22541436
1312496	Med13	mediator complex subunit 13	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170202	MGI			PMID:22541436
1312499	Il4i1	interleukin 4 induced 1	gene	MP:0001454	abnormal cued conditioning behavior		IEA		N	RGD:5509061	20111116	MGI			
1312499	Il4i1	interleukin 4 induced 1	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1312499	Il4i1	interleukin 4 induced 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312499	Il4i1	interleukin 4 induced 1	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906134
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20241121	MGI			
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906134
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906134
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20180927	MGI			PMID:29769718
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906134
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20180927	MGI			PMID:29769718
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906134
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906134
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20180927	MGI			PMID:29769718
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906134
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906134
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20150219	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20241121	MGI			
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0010688	hair follicle outer root sheath hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906134
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180927	MGI			PMID:29769718
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0011999	abnormal tail length		IEA		N	RGD:5509061	20241121	MGI			
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0015068	decreased myocardial fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:25422440
1312501	Aars1	alanyl-tRNA synthetase 1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:25422440
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0010995	abnormal lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0011078	increased macrophage cytokine production		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1312503	Rc3h2	ring finger and CCCH-type zinc finger domains 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1312506	Calhm6	calcium homeostasis modulator family member 6	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20211021	MGI			
1312506	Calhm6	calcium homeostasis modulator family member 6	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1312510	Hdac2	histone deacetylase 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:23696608
1312510	Hdac2	histone deacetylase 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1312510	Hdac2	histone deacetylase 2	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1312510	Hdac2	histone deacetylase 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19424149
1312510	Hdac2	histone deacetylase 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1312510	Hdac2	histone deacetylase 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1312510	Hdac2	histone deacetylase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19424149
1312510	Hdac2	histone deacetylase 2	gene	MP:0001267	enlarged chest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0001282	short vibrissae		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1312510	Hdac2	histone deacetylase 2	gene	MP:0001491	unresponsive to tactile stimuli		IEA		N	RGD:5509061	20240523	MGI			
1312510	Hdac2	histone deacetylase 2	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1312510	Hdac2	histone deacetylase 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19424149
1312510	Hdac2	histone deacetylase 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1312510	Hdac2	histone deacetylase 2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1312510	Hdac2	histone deacetylase 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19424149
1312510	Hdac2	histone deacetylase 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0003429	insensitivity to growth hormone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260402	MGI			PMID:39201474
1312510	Hdac2	histone deacetylase 2	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0004027	trisomy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0004093	diffuse Z line		IAGP		N	RGD:5509061	20180531	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1312510	Hdac2	histone deacetylase 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20150205	MGI			PMID:23696608
1312510	Hdac2	histone deacetylase 2	gene	MP:0005573	increased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21474102
1312510	Hdac2	histone deacetylase 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19424149
1312510	Hdac2	histone deacetylase 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0009309	increased small intestine adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19424149
1312510	Hdac2	histone deacetylase 2	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1312510	Hdac2	histone deacetylase 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19424149
1312510	Hdac2	histone deacetylase 2	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1312510	Hdac2	histone deacetylase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150205	MGI			PMID:23696608
1312510	Hdac2	histone deacetylase 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1312510	Hdac2	histone deacetylase 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19424149
1312510	Hdac2	histone deacetylase 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0011392	increased fetal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20250605	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20240118	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:17639084
1312510	Hdac2	histone deacetylase 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1312510	Hdac2	histone deacetylase 2	gene	MP:0011963	abnormal total retina thickness		IAGP		N	RGD:5509061	20150205	MGI			PMID:23696608
1312510	Hdac2	histone deacetylase 2	gene	MP:0012050	decreased susceptilbility to retina ischemic injury		IAGP		N	RGD:5509061	20150205	MGI			PMID:23696608
1312510	Hdac2	histone deacetylase 2	gene	MP:0012404	abnormal nail color		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1312510	Hdac2	histone deacetylase 2	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:20194438
1312510	Hdac2	histone deacetylase 2	gene	MP:0013916	decreased intestine length		IAGP		N	RGD:5509061	20180719	MGI			PMID:17909008
1312510	Hdac2	histone deacetylase 2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:17322895
1312510	Hdac2	histone deacetylase 2	gene	MP:0030564	thick myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:17322895
1312513	Ctdspl	CTD small phosphatase like	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20160421	MGI			
1312513	Ctdspl	CTD small phosphatase like	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1312513	Ctdspl	CTD small phosphatase like	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1312513	Ctdspl	CTD small phosphatase like	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1312516	Uck2	uridine-cytidine kinase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20201022	MGI			
1312516	Uck2	uridine-cytidine kinase 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1312516	Uck2	uridine-cytidine kinase 2	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729965
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729965
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729965
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0008402	increased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20181220	MGI			PMID:14729965
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20181220	MGI			PMID:14729965
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0010207	abnormal telomere morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:16142233
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729965
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:14729965
1312518	Ercc4	excision repair cross-complementing rodent repair deficiency, complementation group 4	gene	MP:0020427	increased hepatocyte karyomegaly		IAGP		N	RGD:5509061	20181220	MGI			PMID:14729965
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20150611	MGI			PMID:18773073
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20150611	MGI			PMID:18773073
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0005432	abnormal pro-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20150611	MGI			PMID:18773073
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0013207	absent endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604513
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0014403	decreased early pro-B cell number		IAGP		N	RGD:5509061	20240405	MGI			PMID:22427636
1312525	Smarcc1	SWI/SNF related BAF chromatin remodeling complex subunit C1	gene	MP:0014404	decreased late pro-B cell number		IAGP		N	RGD:5509061	20240405	MGI			PMID:22427636
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0010702	split cervical atlas		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0010703	split cervical axis		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0010730	absent odontoid process		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312527	Cdk10	cyclin dependent kinase 10	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20181025	MGI			PMID:28886341
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902388
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:18697905
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1312530	Dlx2	distal-less homeobox 2	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001068	abnormal mandibular nerve branching		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902388
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902388
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902388
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902388
1312530	Dlx2	distal-less homeobox 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1312530	Dlx2	distal-less homeobox 2	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20171005	MGI			PMID:18697905
1312530	Dlx2	distal-less homeobox 2	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902388
1312530	Dlx2	distal-less homeobox 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1312530	Dlx2	distal-less homeobox 2	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0004456	small pterygoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0004666	absent stapedial artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1312530	Dlx2	distal-less homeobox 2	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0009882	absent palatal shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1312530	Dlx2	distal-less homeobox 2	gene	MP:0009917	abnormal hyoid bone body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1312530	Dlx2	distal-less homeobox 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1312530	Dlx2	distal-less homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902388
1312530	Dlx2	distal-less homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1312530	Dlx2	distal-less homeobox 2	gene	MP:0030108	abnormal incudostapedial joint morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0030108	abnormal incudostapedial joint morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0030127	small stapes		IAGP		N	RGD:5509061	20170928	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0030395	absent incus short process		IAGP		N	RGD:5509061	20171207	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0030395	absent incus short process		IAGP		N	RGD:5509061	20171207	MGI			PMID:9187081
1312530	Dlx2	distal-less homeobox 2	gene	MP:0030406	absent stapes obturator foramen		IAGP		N	RGD:5509061	20171207	MGI			PMID:7590232
1312530	Dlx2	distal-less homeobox 2	gene	MP:0030406	absent stapes obturator foramen		IAGP		N	RGD:5509061	20171207	MGI			PMID:9187081
1312533	Capn7	calpain 7	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20111116	MGI			
1312533	Capn7	calpain 7	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20111116	MGI			
1312533	Capn7	calpain 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1312536	Slf1	SMC5-SMC6 complex localization factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632077
1312538	Vps39	VPS39 HOPS complex subunit	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20211104	MGI			PMID:20961651
1312538	Vps39	VPS39 HOPS complex subunit	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20211104	MGI			PMID:20961651
1312540	Sh3glb1	SH3-domain GRB2-like B1 (endophilin)	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16227588
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974926
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974926
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023342
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974926
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20181011	MGI			
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023342
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023342
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023342
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244673
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20181011	MGI			
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008206	increased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023342
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023342
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023342
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023342
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023342
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752681
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0013452	increased lacrimal gland apoptosis		IAGP		N	RGD:5509061	20150205	MGI			PMID:17898284
1312547	Tnfrsf9	tumor necrosis factor receptor superfamily, member 9	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:17608689
1312549	Tfap2d	transcription factor AP-2, delta	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858141
1312549	Tfap2d	transcription factor AP-2, delta	gene	MP:0009039	absent inferior colliculus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21858141
1312553	Lrrtm3	leucine rich repeat transmembrane neuronal 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180920	MGI			PMID:22710909
1312553	Lrrtm3	leucine rich repeat transmembrane neuronal 3	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20180920	MGI			PMID:26776509
1312553	Lrrtm3	leucine rich repeat transmembrane neuronal 3	gene	MP:0002915	abnormal synaptic depression		IAGP		N	RGD:5509061	20180920	MGI			PMID:26776509
1312553	Lrrtm3	leucine rich repeat transmembrane neuronal 3	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20180920	MGI			PMID:26776509
1312553	Lrrtm3	leucine rich repeat transmembrane neuronal 3	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20180920	MGI			PMID:26776509
1312553	Lrrtm3	leucine rich repeat transmembrane neuronal 3	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20180920	MGI			PMID:26776509
1312553	Lrrtm3	leucine rich repeat transmembrane neuronal 3	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20180920	MGI			PMID:26776509
1312553	Lrrtm3	leucine rich repeat transmembrane neuronal 3	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20180920	MGI			PMID:26776509
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20160804	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0002747	abnormal aortic valve morphology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0005244	hemopericardium		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0008922	abnormal cervical rib		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0009820	abnormal liver vasculature morphology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0011513	abnormal vertebral artery morphology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013875	increased trigeminal neuroma incidence		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013878	abnormal ductus venosus valve topology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013936	abnormal thymus topology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013975	abnormal coronary sinus connection		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0014018	embryo tumor		IEA		N	RGD:5509061	20171228	MGI			
1312558	Prmt7	protein arginine N-methyltransferase 7	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20171228	MGI			
1312563	Ifit1bl2	interferon induced protein with tetratricopeptide repeats 1B like 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1312563	Ifit1bl2	interferon induced protein with tetratricopeptide repeats 1B like 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20200514	MGI			
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0001881	abnormal mammary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847332
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847332
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847332
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0011707	impaired fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:20534669
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0013718	galactostasis		IAGP		N	RGD:5509061	20150402	MGI			PMID:16847332
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0013718	galactostasis		IAGP		N	RGD:5509061	20150402	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0013719	pale mammary gland		IAGP		N	RGD:5509061	20150402	MGI			PMID:16847332
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0013719	pale mammary gland		IAGP		N	RGD:5509061	20150402	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0013778	abnormal mammary gland myoepithelium morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:16847332
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0013779	abnormal mammary gland myoepithelium physiology		IAGP		N	RGD:5509061	20150611	MGI			PMID:16847332
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0013779	abnormal mammary gland myoepithelium physiology		IAGP		N	RGD:5509061	20150611	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:16847332
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:16847333
1312565	Mrtfa	myocardin related transcription factor A	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:16847333
1312568	Dlx3	distal-less homeobox 3	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1312568	Dlx3	distal-less homeobox 3	gene	MP:0000288	abnormal pericardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874789
1312568	Dlx3	distal-less homeobox 3	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0000392	accelerated hair follicle regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874789
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874789
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874789
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1312568	Dlx3	distal-less homeobox 3	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1312568	Dlx3	distal-less homeobox 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1312568	Dlx3	distal-less homeobox 3	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874789
1312568	Dlx3	distal-less homeobox 3	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1312568	Dlx3	distal-less homeobox 3	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874789
1312568	Dlx3	distal-less homeobox 3	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874789
1312568	Dlx3	distal-less homeobox 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684741
1312568	Dlx3	distal-less homeobox 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874789
1312568	Dlx3	distal-less homeobox 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312568	Dlx3	distal-less homeobox 3	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1312568	Dlx3	distal-less homeobox 3	gene	MP:0030574	increased hair follicle cell proliferation		IAGP		N	RGD:5509061	20181129	MGI			PMID:18684741
1312573	Atg2b	autophagy related 2B	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210128	MGI			
1312573	Atg2b	autophagy related 2B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1312573	Atg2b	autophagy related 2B	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1312573	Atg2b	autophagy related 2B	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20220811	MGI			
1312573	Atg2b	autophagy related 2B	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1312573	Atg2b	autophagy related 2B	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20231207	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20231207	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20231207	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20250508	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20231207	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0013763	increased T-helper cell number		IEA		N	RGD:5509061	20241121	MGI			
1312576	Dcaf15	DDB1 and CUL4 associated factor 15	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20241121	MGI			
1312577	Cts6	cathepsin 6	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20190502	MGI			
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191128	MGI			
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191128	MGI			
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191128	MGI			
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191128	MGI			
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20190502	MGI			
1312579	Clpx	caseinolytic mitochondrial matrix peptidase chaperone subunit	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241128	MGI			
1312580	6430548M08Rik	RIKEN cDNA 6430548M08 gene	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1312580	6430548M08Rik	RIKEN cDNA 6430548M08 gene	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1312580	6430548M08Rik	RIKEN cDNA 6430548M08 gene	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1312580	6430548M08Rik	RIKEN cDNA 6430548M08 gene	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1312580	6430548M08Rik	RIKEN cDNA 6430548M08 gene	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1312580	6430548M08Rik	RIKEN cDNA 6430548M08 gene	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20241121	MGI			
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0008105	increased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19945391
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20250508	MGI			
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1312584	Dscaml1	DS cell adhesion molecule like 1	gene	MP:0014265	thick retina inner plexiform layer		IAGP		N	RGD:5509061	20230706	MGI			PMID:19945391
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555074
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555074
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0003663	abnormal thermosensation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555074
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0005199	abnormal iris pigment epithelium		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555074
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0010055	abnormal sensory neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555074
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0010259	anterior polar cataract		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0010768	mortality/aging		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312586	Trpm3	transient receptor potential cation channel, subfamily M, member 3	gene	MP:0020486	abnormal lens topology		IAGP		N	RGD:5509061	20210812	MGI			PMID:33484482
1312587	Gpr18	G protein-coupled receptor 18	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20170525	MGI			PMID:26195725
1312587	Gpr18	G protein-coupled receptor 18	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20170525	MGI			PMID:26195725
1312587	Gpr18	G protein-coupled receptor 18	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160310	MGI			PMID:25348153
1312587	Gpr18	G protein-coupled receptor 18	gene	MP:0008363	decreased CD8-positive, gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20160310	MGI			PMID:25348153
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20170518	MGI			PMID:24646517
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000486	abnormal pulmonary trunk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922872
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25757017
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922872
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922872
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922872
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20170518	MGI			PMID:24646517
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922872
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922872
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004648	decreased thoracic vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922872
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20170518	MGI			PMID:24646517
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19264921
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651658
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:16702405
1312591	Kat6a	K(lysine) acetyltransferase 6A	gene	MP:0015008	abnormal fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:16651658
1312593	Ccr8	C-C motif chemokine receptor 8	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1312593	Ccr8	C-C motif chemokine receptor 8	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1312593	Ccr8	C-C motif chemokine receptor 8	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1312593	Ccr8	C-C motif chemokine receptor 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496446
1312593	Ccr8	C-C motif chemokine receptor 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574386
1312593	Ccr8	C-C motif chemokine receptor 8	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471141
1312593	Ccr8	C-C motif chemokine receptor 8	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1312593	Ccr8	C-C motif chemokine receptor 8	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1312597	Ddx31	DEAD/H box helicase 31	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220811	MGI			
1312597	Ddx31	DEAD/H box helicase 31	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1312602	Prtn3	proteinase 3	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25180606
1312602	Prtn3	proteinase 3	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25180606
1312602	Prtn3	proteinase 3	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20160225	MGI			PMID:25180606
1312604	Myt1	myelin transcription factor 1	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928203
1312604	Myt1	myelin transcription factor 1	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928203
1312604	Myt1	myelin transcription factor 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928203
1312604	Myt1	myelin transcription factor 1	gene	MP:0003563	abnormal pancreatic alpha cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928203
1312604	Myt1	myelin transcription factor 1	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928203
1312604	Myt1	myelin transcription factor 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928203
1312604	Myt1	myelin transcription factor 1	gene	MP:0008953	abnormal pancreatic somatostatin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928203
1312604	Myt1	myelin transcription factor 1	gene	MP:0009195	abnormal PP cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928203
1312604	Myt1	myelin transcription factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21267777
1312604	Myt1	myelin transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928203
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20240425	MGI			PMID:21052544
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20160421	MGI			
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861548
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0002546	mydriasis		IEA		N	RGD:5509061	20190502	MGI			
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896717
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20240425	MGI			PMID:21052544
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861548
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966281
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896717
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861548
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966281
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861548
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861548
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21052544
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20190502	MGI			
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0008519	thin retina outer plexiform layer		IEA		N	RGD:5509061	20240425	MGI			
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0012029	abnormal electroretinogram waveform feature		IEA		N	RGD:5509061	20240425	MGI			
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0012671	retina spots		IEA		N	RGD:5509061	20240425	MGI			
1312608	Trpm1	transient receptor potential cation channel, subfamily M, member 1	gene	MP:0020439	absent b-wave		IEA		N	RGD:5509061	20240425	MGI			
1312609	Nlrc3	NLR family, CARD domain containing 3	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863753
1312609	Nlrc3	NLR family, CARD domain containing 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863753
1312609	Nlrc3	NLR family, CARD domain containing 3	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863753
1312609	Nlrc3	NLR family, CARD domain containing 3	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863753
1312609	Nlrc3	NLR family, CARD domain containing 3	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863753
1312609	Nlrc3	NLR family, CARD domain containing 3	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863753
1312609	Nlrc3	NLR family, CARD domain containing 3	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:22863753
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0004846	absent skeletal muscle		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0004938	dilated vasculature		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0006093	arteriovenous malformation		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0010572	persistent right dorsal aorta		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0011697	lens vacuoles		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0013826	absent hypoglossal canal		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0013847	retropleural edema		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0013917	persistent right 6th pharyngeal arch artery		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0013953	left sided brachiocephalic trunk		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1312610	Prrc2b	proline-rich coiled-coil 2B	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1312611	Gpat2	glycerol-3-phosphate acyltransferase 2, mitochondrial	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20191114	MGI			PMID:30951587
1312611	Gpat2	glycerol-3-phosphate acyltransferase 2, mitochondrial	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20191114	MGI			PMID:30951587
1312611	Gpat2	glycerol-3-phosphate acyltransferase 2, mitochondrial	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20191114	MGI			PMID:30951587
1312611	Gpat2	glycerol-3-phosphate acyltransferase 2, mitochondrial	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20191114	MGI			PMID:30951587
1312611	Gpat2	glycerol-3-phosphate acyltransferase 2, mitochondrial	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:30951587
1312611	Gpat2	glycerol-3-phosphate acyltransferase 2, mitochondrial	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:30951587
1312611	Gpat2	glycerol-3-phosphate acyltransferase 2, mitochondrial	gene	MP:0008878	abnormal DNA methylation during gametogenesis		IAGP		N	RGD:5509061	20191114	MGI			PMID:30951587
1312611	Gpat2	glycerol-3-phosphate acyltransferase 2, mitochondrial	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20191114	MGI			PMID:30951587
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20201022	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20201022	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20201022	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210520	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20201022	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20190502	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1312614	Trappc2l	trafficking protein particle complex 2L	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1312616	Cog2	component of oligomeric golgi complex 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1312616	Cog2	component of oligomeric golgi complex 2	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1312616	Cog2	component of oligomeric golgi complex 2	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1312616	Cog2	component of oligomeric golgi complex 2	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1312616	Cog2	component of oligomeric golgi complex 2	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20160804	MGI			
1312616	Cog2	component of oligomeric golgi complex 2	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1312616	Cog2	component of oligomeric golgi complex 2	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1312616	Cog2	component of oligomeric golgi complex 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312618	Cenph	centromere protein H	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20221215	MGI			
1312618	Cenph	centromere protein H	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1312618	Cenph	centromere protein H	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312620	Ddx42	DEAD box helicase 42	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1312620	Ddx42	DEAD box helicase 42	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1312620	Ddx42	DEAD box helicase 42	gene	MP:0005477	increased circulating thyroxine level		IEA		N	RGD:5509061	20211021	MGI			
1312620	Ddx42	DEAD box helicase 42	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1312620	Ddx42	DEAD box helicase 42	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312632	Optc	opticin	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22159013
1312635	Asf1b	anti-silencing function 1B histone chaperone	gene	MP:0002497	increased IgE level		IEA		N	RGD:5509061	20190103	MGI			
1312640	Cdc27	cell division cycle 27	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1312640	Cdc27	cell division cycle 27	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1312640	Cdc27	cell division cycle 27	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1312642	Irf2	interferon regulatory factor 2	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312642	Irf2	interferon regulatory factor 2	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312642	Irf2	interferon regulatory factor 2	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17709541
1312642	Irf2	interferon regulatory factor 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312642	Irf2	interferon regulatory factor 2	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312642	Irf2	interferon regulatory factor 2	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
1312642	Irf2	interferon regulatory factor 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312642	Irf2	interferon regulatory factor 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
1312642	Irf2	interferon regulatory factor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
1312642	Irf2	interferon regulatory factor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
1312642	Irf2	interferon regulatory factor 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
1312642	Irf2	interferon regulatory factor 2	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
1312642	Irf2	interferon regulatory factor 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
1312642	Irf2	interferon regulatory factor 2	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312642	Irf2	interferon regulatory factor 2	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312642	Irf2	interferon regulatory factor 2	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312642	Irf2	interferon regulatory factor 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
1312642	Irf2	interferon regulatory factor 2	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8402903
1312642	Irf2	interferon regulatory factor 2	gene	MP:0009623	enlarged inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312642	Irf2	interferon regulatory factor 2	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578362
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578362
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0008179	absent germinal center B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578362
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0009058	decreased interleukin-21 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578362
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0010187	decreased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312644	Batf	basic leucine zipper transcription factor, ATF-like	gene	MP:0010220	decreased T-helper 17 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421391
1312651	Fam135a	family with sequence similarity 135, member A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230119	MGI			
1312651	Fam135a	family with sequence similarity 135, member A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1312651	Fam135a	family with sequence similarity 135, member A	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1312651	Fam135a	family with sequence similarity 135, member A	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1312651	Fam135a	family with sequence similarity 135, member A	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230119	MGI			
1312651	Fam135a	family with sequence similarity 135, member A	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1312651	Fam135a	family with sequence similarity 135, member A	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1312651	Fam135a	family with sequence similarity 135, member A	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230119	MGI			
1312651	Fam135a	family with sequence similarity 135, member A	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230119	MGI			
1312653	Hmx1	H6 homeobox 1	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1312653	Hmx1	H6 homeobox 1	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1312653	Hmx1	H6 homeobox 1	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23591430
1312653	Hmx1	H6 homeobox 1	gene	MP:0008383	enlarged gonial bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23591430
1312653	Hmx1	H6 homeobox 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0030119	abnormal retrotympanic process morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:19379485
1312653	Hmx1	H6 homeobox 1	gene	MP:0030213	gonial bone hyperplasia		IAGP		N	RGD:5509061	20171019	MGI			PMID:19379485
1312655	Rubcnl	RUN and cysteine rich domain containing beclin 1 interacting protein like	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20191010	MGI			PMID:30704899
1312655	Rubcnl	RUN and cysteine rich domain containing beclin 1 interacting protein like	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20191010	MGI			PMID:30704899
1312655	Rubcnl	RUN and cysteine rich domain containing beclin 1 interacting protein like	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20191010	MGI			PMID:30704899
1312655	Rubcnl	RUN and cysteine rich domain containing beclin 1 interacting protein like	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20191010	MGI			PMID:30704899
1312655	Rubcnl	RUN and cysteine rich domain containing beclin 1 interacting protein like	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20191010	MGI			PMID:30704899
1312655	Rubcnl	RUN and cysteine rich domain containing beclin 1 interacting protein like	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20191010	MGI			PMID:30704899
1312655	Rubcnl	RUN and cysteine rich domain containing beclin 1 interacting protein like	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20191010	MGI			PMID:30704899
1312655	Rubcnl	RUN and cysteine rich domain containing beclin 1 interacting protein like	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20191010	MGI			PMID:30704899
1312657	Perm1	PPARGC1 and ESRR induced regulator, muscle 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20230406	MGI			PMID:36419485
1312659	Haus3	HAUS augmin-like complex, subunit 3	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118569
1312668	Exoc1	exocyst complex component 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1312668	Exoc1	exocyst complex component 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20170330	MGI			PMID:26346620
1312668	Exoc1	exocyst complex component 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312668	Exoc1	exocyst complex component 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1312670	Atf7	activating transcription factor 7	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20190502	MGI			
1312670	Atf7	activating transcription factor 7	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201022	MGI			
1312670	Atf7	activating transcription factor 7	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893493
1312670	Atf7	activating transcription factor 7	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893493
1312670	Atf7	activating transcription factor 7	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312670	Atf7	activating transcription factor 7	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893493
1312670	Atf7	activating transcription factor 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699753
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702766
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1312672	Hipk1	homeodomain interacting protein kinase 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844119
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844119
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844119
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844119
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844119
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844119
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0004836	abnormal synaptic acetylcholine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844119
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0009426	decreased soleus weight		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:11583983
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0030950	abnormal synaptic vesicle exocytosis		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312682	Col13a1	collagen, type XIII, alpha 1	gene	MP:0030951	abnormal endocytosis		IAGP		N	RGD:5509061	20190725	MGI			PMID:28369367
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431509
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431509
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431509
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28041882
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20190221	MGI			PMID:29244146
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20240328	MGI			PMID:38015625
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390661
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311137
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20190221	MGI			PMID:29244146
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311137
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431509
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390661
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390661
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496962
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496962
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20190221	MGI			PMID:29244146
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20190221	MGI			PMID:29244146
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20190221	MGI			PMID:29244146
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390661
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19026780
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215809
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0004514	dystocia		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20190221	MGI			PMID:29244146
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38015625
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431509
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431509
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680150
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0005432	abnormal pro-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496962
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680150
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496962
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496962
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680150
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680150
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680150
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680150
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680150
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008755	abnormal immunoglobulin V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496962
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0008876	decreased uterine NK cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0009094	abnormal endometrial gland morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19755104
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0010682	abnormal hair follicle infundibulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0010684	abnormal hair follicle outer root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20190221	MGI			PMID:29244146
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22215809
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190221	MGI			PMID:29244146
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496962
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390661
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311137
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19026780
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20240328	MGI			PMID:38015625
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20181129	MGI			PMID:21317239
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0011873	enlarged uterine horn		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390661
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20211209	MGI			PMID:30954472
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20180607	MGI			PMID:28041882
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0013620	increased internal diameter of femur		IAGP		N	RGD:5509061	20240328	MGI			PMID:38015625
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0013623	increased femur compact bone thickness		IAGP		N	RGD:5509061	20240328	MGI			PMID:38015625
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0014519	myocardial ventricular hypertrabeculation		IAGP		N	RGD:5509061	20240822	MGI			PMID:22215809
1312684	Ezh2	enhancer of zeste 2 polycomb repressive complex 2 subunit	gene	MP:0031336	abnormal uterine epithelium development		IAGP		N	RGD:5509061	20220120	MGI			PMID:30954472
1312686	Card10	caspase recruitment domain family, member 10	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438001
1312686	Card10	caspase recruitment domain family, member 10	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438001
1312688	Il21r	interleukin 21 receptor	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1312688	Il21r	interleukin 21 receptor	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20111116	MGI			
1312688	Il21r	interleukin 21 receptor	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
1312688	Il21r	interleukin 21 receptor	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446913
1312688	Il21r	interleukin 21 receptor	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446913
1312688	Il21r	interleukin 21 receptor	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1312688	Il21r	interleukin 21 receptor	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1312688	Il21r	interleukin 21 receptor	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446913
1312688	Il21r	interleukin 21 receptor	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446913
1312688	Il21r	interleukin 21 receptor	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0002607	decreased basophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20201022	MGI			
1312688	Il21r	interleukin 21 receptor	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630141
1312688	Il21r	interleukin 21 receptor	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18546146
1312688	Il21r	interleukin 21 receptor	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20180111	MGI			PMID:19164519
1312688	Il21r	interleukin 21 receptor	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779574
1312688	Il21r	interleukin 21 receptor	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630141
1312688	Il21r	interleukin 21 receptor	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779574
1312688	Il21r	interleukin 21 receptor	gene	MP:0005362	abnormal Langerhans cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
1312688	Il21r	interleukin 21 receptor	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
1312688	Il21r	interleukin 21 receptor	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
1312688	Il21r	interleukin 21 receptor	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474630
1312688	Il21r	interleukin 21 receptor	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779574
1312688	Il21r	interleukin 21 receptor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446913
1312688	Il21r	interleukin 21 receptor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
1312688	Il21r	interleukin 21 receptor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446913
1312688	Il21r	interleukin 21 receptor	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446913
1312688	Il21r	interleukin 21 receptor	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
1312688	Il21r	interleukin 21 receptor	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446913
1312688	Il21r	interleukin 21 receptor	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446913
1312688	Il21r	interleukin 21 receptor	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312688	Il21r	interleukin 21 receptor	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
1312688	Il21r	interleukin 21 receptor	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
1312688	Il21r	interleukin 21 receptor	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581537
1312688	Il21r	interleukin 21 receptor	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
1312688	Il21r	interleukin 21 receptor	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779574
1312688	Il21r	interleukin 21 receptor	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
1312688	Il21r	interleukin 21 receptor	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077330
1312688	Il21r	interleukin 21 receptor	gene	MP:0008769	abnormal plasmacytoid dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075398
1312688	Il21r	interleukin 21 receptor	gene	MP:0009058	decreased interleukin-21 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16778988
1312688	Il21r	interleukin 21 receptor	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11970879
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0002918	abnormal paired-pulse facilitation		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0010052	increased grip strength		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0030585	enhanced behavioral response to amphetamine		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312691	Pianp	PILR alpha associated neural protein	gene	MP:0030735	abnormal glutamic acid level		IAGP		N	RGD:5509061	20191031	MGI			PMID:31511635
1312694	Pold2	polymerase (DNA directed), delta 2, regulatory subunit	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20241017	MGI			PMID:36528861
1312694	Pold2	polymerase (DNA directed), delta 2, regulatory subunit	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20240613	MGI			PMID:36528861
1312694	Pold2	polymerase (DNA directed), delta 2, regulatory subunit	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20240613	MGI			PMID:36528861
1312694	Pold2	polymerase (DNA directed), delta 2, regulatory subunit	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20240801	MGI			PMID:36528861
1312694	Pold2	polymerase (DNA directed), delta 2, regulatory subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312694	Pold2	polymerase (DNA directed), delta 2, regulatory subunit	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20260402	MGI			
1312694	Pold2	polymerase (DNA directed), delta 2, regulatory subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312696	Armc3	armadillo repeat containing 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20211216	MGI			PMID:34428398
1312696	Armc3	armadillo repeat containing 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20211216	MGI			PMID:34428398
1312696	Armc3	armadillo repeat containing 3	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20241121	MGI			
1312696	Armc3	armadillo repeat containing 3	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20211216	MGI			PMID:34428398
1312696	Armc3	armadillo repeat containing 3	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20211216	MGI			PMID:34428398
1312696	Armc3	armadillo repeat containing 3	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20211216	MGI			PMID:34428398
1312697	Ebf3	early B cell factor 3	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993187
1312697	Ebf3	early B cell factor 3	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993187
1312697	Ebf3	early B cell factor 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993187
1312697	Ebf3	early B cell factor 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1312697	Ebf3	early B cell factor 3	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993187
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293286
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16690048
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16690048
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11156601
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20969844
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22609278
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11156601
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787067
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22609278
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293286
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22609278
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787067
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:22609278
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001334	absent optic tract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19459208
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16690048
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293286
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22609278
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903076
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006070	increased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787067
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006075	abnormal retina cone bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006075	abnormal retina cone bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092954
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787067
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11156601
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22609278
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11156601
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623245
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787067
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20969844
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903076
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293286
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11156601
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008068	absent retina ganglion cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008068	absent retina ganglion cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787067
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008105	increased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11156601
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008105	increased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092954
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008445	increased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008445	increased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008510	absent retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20969844
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11156601
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493566
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23481413
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20171012	MGI			PMID:15980246
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0020548	decreased optic chiasm size		IAGP		N	RGD:5509061	20180301	MGI			PMID:11156601
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:18321480
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:18787067
1312699	Atoh7	atonal bHLH transcription factor 7	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:23481413
1312702	Rdh13	retinol dehydrogenase 13 (all-trans and 9-cis)	gene	MP:0003312	abnormal locomotor coordination		IEA		N	RGD:5509061	20170413	MGI			
1312702	Rdh13	retinol dehydrogenase 13 (all-trans and 9-cis)	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22605914
1312702	Rdh13	retinol dehydrogenase 13 (all-trans and 9-cis)	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22605914
1312702	Rdh13	retinol dehydrogenase 13 (all-trans and 9-cis)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22605914
1312702	Rdh13	retinol dehydrogenase 13 (all-trans and 9-cis)	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22605914
1312702	Rdh13	retinol dehydrogenase 13 (all-trans and 9-cis)	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22605914
1312702	Rdh13	retinol dehydrogenase 13 (all-trans and 9-cis)	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22605914
1312706	Wbp1	WW domain binding protein 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1312706	Wbp1	WW domain binding protein 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
1312706	Wbp1	WW domain binding protein 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1312706	Wbp1	WW domain binding protein 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25616964
1312708	Pcare	photoreceptor cilium actin regulator	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:25616964
1312710	Aifm2	apoptosis-inducing factor, mitochondrion-associated 2	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186796
1312712	Rhoc	ras homolog family member C	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107613
1312712	Rhoc	ras homolog family member C	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107613
1312712	Rhoc	ras homolog family member C	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107613
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385121
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385121
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668681
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385121
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385121
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385121
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385121
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0004712	notochord degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385121
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385121
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668681
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10385121
1312721	Stil	Scl/Tal1 interrupting locus	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668681
1312723	Mospd3	motile sperm domain containing 3	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15533722
1312723	Mospd3	motile sperm domain containing 3	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15533722
1312723	Mospd3	motile sperm domain containing 3	gene	MP:0000486	abnormal pulmonary trunk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15533722
1312723	Mospd3	motile sperm domain containing 3	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15533722
1312723	Mospd3	motile sperm domain containing 3	gene	MP:0004061	papillary muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15533722
1312723	Mospd3	motile sperm domain containing 3	gene	MP:0010428	abnormal heart right ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15533722
1312723	Mospd3	motile sperm domain containing 3	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20231221	MGI			PMID:15533722
1312723	Mospd3	motile sperm domain containing 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15533722
1312723	Mospd3	motile sperm domain containing 3	gene	MP:0021160	decreased heart right ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:15533722
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15122331
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15122331
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15122331
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15122331
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009599
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009599
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15122331
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15122331
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009599
1312726	Rad52	RAD52 homolog, DNA repair protein	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15122331
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0003326	liver failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312731	Usp8	ubiquitin specific peptidase 8	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452457
1312735	Lpxn	leupaxin	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20210617	MGI			PMID:32269569
1312735	Lpxn	leupaxin	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20210617	MGI			PMID:32269569
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20210128	MGI			
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20210128	MGI			
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0011344	abnormal loop of Henle ascending limb thick segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20180222	MGI			PMID:21685914
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312739	Sec63	SEC63 homolog, protein translocation regulator	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1312743	Mettl9	methyltransferase like 9	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20210506	MGI			PMID:33563959
1312745	Wnt10b	wingless-type MMTV integration site family, member 10B	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1312745	Wnt10b	wingless-type MMTV integration site family, member 10B	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210128	MGI			
1312745	Wnt10b	wingless-type MMTV integration site family, member 10B	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15673614
1312745	Wnt10b	wingless-type MMTV integration site family, member 10B	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15673614
1312745	Wnt10b	wingless-type MMTV integration site family, member 10B	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20181227	MGI			
1312745	Wnt10b	wingless-type MMTV integration site family, member 10B	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20181227	MGI			
1312745	Wnt10b	wingless-type MMTV integration site family, member 10B	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20190502	MGI			
1312747	Tnfrsf25	tumor necrosis factor receptor superfamily, member 25	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313471
1312747	Tnfrsf25	tumor necrosis factor receptor superfamily, member 25	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313471
1312747	Tnfrsf25	tumor necrosis factor receptor superfamily, member 25	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313471
1312747	Tnfrsf25	tumor necrosis factor receptor superfamily, member 25	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313471
1312747	Tnfrsf25	tumor necrosis factor receptor superfamily, member 25	gene	MP:0004918	abnormal negative T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313471
1312747	Tnfrsf25	tumor necrosis factor receptor superfamily, member 25	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313471
1312747	Tnfrsf25	tumor necrosis factor receptor superfamily, member 25	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0000928	incomplete rostral neuropore closure		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0012099	decreased spongiotrophoblast size		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0012270	cardiac edema		IEA		N	RGD:5509061	20251204	MGI			
1312749	Kctd5	potassium channel tetramerisation domain containing 5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210520	MGI			
1312750	Thoc5	THO complex 5	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312750	Thoc5	THO complex 5	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051105
1312754	Drg1	developmentally regulated GTP binding protein 1	gene	MP:0000613	abnormal salivary gland morphology		IEA		N	RGD:5509061	20230119	MGI			
1312754	Drg1	developmentally regulated GTP binding protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1312754	Drg1	developmentally regulated GTP binding protein 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230119	MGI			
1312754	Drg1	developmentally regulated GTP binding protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:37179472
1312756	Cebpz	CCAAT/enhancer binding protein zeta	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1312760	Kif1a	kinesin family member 1A	gene	MP:0000755	hindlimb paralysis		IEA		N	RGD:5509061	20160407	MGI			
1312760	Kif1a	kinesin family member 1A	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20160407	MGI			
1312760	Kif1a	kinesin family member 1A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0003312	abnormal locomotor coordination		IEA		N	RGD:5509061	20160407	MGI			
1312760	Kif1a	kinesin family member 1A	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0004263	abnormal limb posture		IEA		N	RGD:5509061	20160407	MGI			
1312760	Kif1a	kinesin family member 1A	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9548721
1312760	Kif1a	kinesin family member 1A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20160407	MGI			
1312760	Kif1a	kinesin family member 1A	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20160407	MGI			
1312762	Sec61b	SEC61 translocon subunit beta	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210128	MGI			
1312762	Sec61b	SEC61 translocon subunit beta	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1312762	Sec61b	SEC61 translocon subunit beta	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20231207	MGI			
1312764	Ddx21	DExD box helicase 21	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1312764	Ddx21	DExD box helicase 21	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1312764	Ddx21	DExD box helicase 21	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241010	MGI			
1312764	Ddx21	DExD box helicase 21	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141003	MGI			
1312764	Ddx21	DExD box helicase 21	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1312764	Ddx21	DExD box helicase 21	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20160421	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20160421	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0003064	decreased coping response		IEA		N	RGD:5509061	20160421	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20221215	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20220811	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160421	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20160421	MGI			
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0012147	increased a-wave implicit time		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0012150	increased b-wave implicit time		IAGP		N	RGD:5509061	20150122	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:24833722
1312765	Fam161a	family with sequence similarity 161, member A	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:24833722
1312767	Cldn19	claudin 19	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883201
1312767	Cldn19	claudin 19	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883201
1312767	Cldn19	claudin 19	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883201
1312767	Cldn19	claudin 19	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20240523	MGI			
1312767	Cldn19	claudin 19	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1312767	Cldn19	claudin 19	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1312767	Cldn19	claudin 19	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20211021	MGI			
1312767	Cldn19	claudin 19	gene	MP:0010571	shortened ST segment		IEA		N	RGD:5509061	20210128	MGI			
1312767	Cldn19	claudin 19	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20170105	MGI			
1312767	Cldn19	claudin 19	gene	MP:0011954	shortened PQ interval		IEA		N	RGD:5509061	20210128	MGI			
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20111116	MGI			
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314502
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133585
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133585
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22240097
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133585
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0004196	abnormal prenatal growth/weight/body size		IAGP		N	RGD:5509061	20160331	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314502
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133585
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0005459	decreased percent body fat/body weight		IEA		N	RGD:5509061	20111116	MGI			
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314502
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314502
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133585
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133585
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133585
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314502
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22240097
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847320
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314502
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0012159	absent anterior visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826531
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312772	Pknox1	Pbx/knotted 1 homeobox	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220324	MGI			PMID:29293683
1312774	Sfswap	splicing factor SWAP	gene	MP:0000026	abnormal inner ear morphology		IEA		N	RGD:5509061	20111116	MGI			
1312774	Sfswap	splicing factor SWAP	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1312774	Sfswap	splicing factor SWAP	gene	MP:0003491	abnormal voluntary movement		IEA		N	RGD:5509061	20111116	MGI			
1312774	Sfswap	splicing factor SWAP	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20240523	MGI			
1312774	Sfswap	splicing factor SWAP	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20240523	MGI			
1312774	Sfswap	splicing factor SWAP	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1312774	Sfswap	splicing factor SWAP	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20231207	MGI			
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20191114	MGI			PMID:29259128
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20191114	MGI			PMID:29259128
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:29259128
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20191114	MGI			PMID:29259128
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20191114	MGI			PMID:29259128
1312776	Lamtor5	late endosomal/lysosomal adaptor, MAPK and MTOR activator 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312780	Suclg2	succinate-Coenzyme A ligase, GDP-forming, beta subunit	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1312780	Suclg2	succinate-Coenzyme A ligase, GDP-forming, beta subunit	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1312780	Suclg2	succinate-Coenzyme A ligase, GDP-forming, beta subunit	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1312780	Suclg2	succinate-Coenzyme A ligase, GDP-forming, beta subunit	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1312780	Suclg2	succinate-Coenzyme A ligase, GDP-forming, beta subunit	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1312780	Suclg2	succinate-Coenzyme A ligase, GDP-forming, beta subunit	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1312780	Suclg2	succinate-Coenzyme A ligase, GDP-forming, beta subunit	gene	MP:0014388	decreased hepatocyte mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:27496549
1312782	Dnajc9	DnaJ heat shock protein family (Hsp40) member C9	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20181227	MGI			
1312782	Dnajc9	DnaJ heat shock protein family (Hsp40) member C9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312782	Dnajc9	DnaJ heat shock protein family (Hsp40) member C9	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1312782	Dnajc9	DnaJ heat shock protein family (Hsp40) member C9	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1312784	C1qtnf3	C1q and tumor necrosis factor related protein 3	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24269820
1312784	C1qtnf3	C1q and tumor necrosis factor related protein 3	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24269820
1312784	C1qtnf3	C1q and tumor necrosis factor related protein 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20221215	MGI			
1312784	C1qtnf3	C1q and tumor necrosis factor related protein 3	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24269820
1312784	C1qtnf3	C1q and tumor necrosis factor related protein 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20221215	MGI			
1312784	C1qtnf3	C1q and tumor necrosis factor related protein 3	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20221215	MGI			
1312791	2310057M21Rik	RIKEN cDNA 2310057M21 gene	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:32869547
1312791	2310057M21Rik	RIKEN cDNA 2310057M21 gene	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20250925	MGI			PMID:32869547
1312793	Pabpc4	poly(A) binding protein, cytoplasmic 4	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20181227	MGI			
1312793	Pabpc4	poly(A) binding protein, cytoplasmic 4	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20160114	MGI			
1312793	Pabpc4	poly(A) binding protein, cytoplasmic 4	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20150108	MGI			
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0003189	fused joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0003843	abnormal sagittal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0004447	small basioccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0008818	abnormal interfrontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0009899	hyoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312798	Wnt9a	wingless-type MMTV integration site family, member 9A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818445
1312800	Cerk	ceramide kinase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292572
1312800	Cerk	ceramide kinase	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292572
1312800	Cerk	ceramide kinase	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292572
1312800	Cerk	ceramide kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292572
1312800	Cerk	ceramide kinase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17888878
1312800	Cerk	ceramide kinase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292572
1312800	Cerk	ceramide kinase	gene	MP:0003867	increased defecation amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17888878
1312800	Cerk	ceramide kinase	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292572
1312800	Cerk	ceramide kinase	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20160721	MGI			PMID:18555012
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19631204
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0006006	increased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19631204
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20201022	MGI			
1312806	Heyl	hairy/enhancer-of-split related with YRPW motif-like	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989910
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0010682	abnormal hair follicle infundibulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0010684	abnormal hair follicle outer root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122289
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317239
1312814	Ezh1	enhancer of zeste 1 polycomb repressive complex 2 subunit	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20181129	MGI			PMID:21317239
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585875
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672539
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620301
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0004798	decreased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0004822	decreased susceptibility to experimental autoimmune uveoretinitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118967
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585875
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672539
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672539
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672539
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585875
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118967
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11672539
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118967
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118967
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18375937
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312816	Il27ra	interleukin 27 receptor, alpha	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004160
1312822	Tmprss4	transmembrane protease, serine 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20161117	MGI			PMID:26309024
1312824	Net1	neuroepithelial cell transforming gene 1	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20160225	MGI			PMID:25321414
1312824	Net1	neuroepithelial cell transforming gene 1	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20160225	MGI			PMID:25321414
1312824	Net1	neuroepithelial cell transforming gene 1	gene	MP:0008904	abnormal mammary fat pad morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25321414
1312824	Net1	neuroepithelial cell transforming gene 1	gene	MP:0013784	abnormal mammary gland bud elongation		IAGP		N	RGD:5509061	20160225	MGI			PMID:25321414
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20201022	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20240523	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220519	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20240523	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220519	MGI			
1312826	Mmaa	methylmalonic aciduria (cobalamin deficiency) type A	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220811	MGI			
1312831	Icam5	intercellular adhesion molecule 5, telencephalin	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135016
1312831	Icam5	intercellular adhesion molecule 5, telencephalin	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20201022	MGI			
1312831	Icam5	intercellular adhesion molecule 5, telencephalin	gene	MP:0002634	abnormal sensorimotor gating		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135016
1312831	Icam5	intercellular adhesion molecule 5, telencephalin	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11135016
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10802667
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10802668
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163633
1312833	Six5	sine oculis-related homeobox 5	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:10802668
1312838	Zan	zonadhesin	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20200102	MGI			PMID:20529856
1312840	Emc7	ER membrane protein complex subunit 7	gene	MP:0010166	increased response to stress-induced hyperthermia		IEA		N	RGD:5509061	20170323	MGI			
1312840	Emc7	ER membrane protein complex subunit 7	gene	MP:0010770	preweaning lethality		IEA		N	RGD:5509061	20170323	MGI			
1312840	Emc7	ER membrane protein complex subunit 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312842	Stk11ip	serine/threonine kinase 11 interacting protein	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20221201	MGI			PMID:33486894
1312842	Stk11ip	serine/threonine kinase 11 interacting protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312842	Stk11ip	serine/threonine kinase 11 interacting protein	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210520	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20160616	MGI			PMID:25432536
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20160616	MGI			PMID:25432536
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20160616	MGI			PMID:25432536
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20160616	MGI			PMID:25432536
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20171228	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0003584	bifid ureter		IEA		N	RGD:5509061	20171228	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0003586	dilated ureter		IEA		N	RGD:5509061	20170504	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0004017	duplex kidney		IEA		N	RGD:5509061	20171228	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20160616	MGI			PMID:25432536
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:24357318
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:24357318
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24357318
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:25432536
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0010484	bicuspid aortic valve		IEA		N	RGD:5509061	20171228	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160616	MGI			PMID:25432536
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24357318
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1312846	Cyfip2	cytoplasmic FMR1 interacting protein 2	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:24357318
1312851	Pgs1	phosphatidylglycerophosphate synthase 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1312851	Pgs1	phosphatidylglycerophosphate synthase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20160804	MGI			
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20160804	MGI			
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:25425145
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20250306	MGI			PMID:25425145
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20250306	MGI			PMID:25425145
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0009870	abnormal abdominal aorta morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0009871	abnormal aorta tunica adventitia morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:25425145
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20250306	MGI			PMID:25425145
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0031274	increased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312853	Arhgap18	Rho GTPase activating protein 18	gene	MP:0031281	increased susceptibility to aneurysm induced morbidity/mortality		IAGP		N	RGD:5509061	20250306	MGI			PMID:28701309
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8356451
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792495
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8356452
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0003063	increased coping response		IEA		N	RGD:5509061	20211021	MGI			
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607487
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792495
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792495
1312855	Dntt	deoxynucleotidyltransferase, terminal	gene	MP:0008761	abnormal immunoglobulin light chain V-J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860755
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0004119	hypokalemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0004410	absent endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0008309	dilated scala media		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0011625	cystolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312857	Atp6v0a4	ATPase, H+ transporting, lysosomal V0 subunit A4	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22872862
1312860	Nagk	N-acetylglucosamine kinase	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1312860	Nagk	N-acetylglucosamine kinase	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1312860	Nagk	N-acetylglucosamine kinase	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1312860	Nagk	N-acetylglucosamine kinase	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1312860	Nagk	N-acetylglucosamine kinase	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20160811	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20210520	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20160421	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20160811	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20160811	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20160421	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20210520	MGI			
1312862	Rab34	RAB34, member RAS oncogene family	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312864	Rbm5	RNA binding motif protein 5	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20160526	MGI			PMID:23935508
1312864	Rbm5	RNA binding motif protein 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160526	MGI			PMID:23935508
1312864	Rbm5	RNA binding motif protein 5	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20160526	MGI			PMID:23935508
1312864	Rbm5	RNA binding motif protein 5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20160526	MGI			PMID:23935508
1312864	Rbm5	RNA binding motif protein 5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20160526	MGI			PMID:23935508
1312864	Rbm5	RNA binding motif protein 5	gene	MP:0006380	abnormal spermatid morphology		IEA		N	RGD:5509061	20141003	MGI			
1312864	Rbm5	RNA binding motif protein 5	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20160526	MGI			PMID:23935508
1312864	Rbm5	RNA binding motif protein 5	gene	MP:0008280	abnormal male germ cell apoptosis		IEA		N	RGD:5509061	20141003	MGI			
1312864	Rbm5	RNA binding motif protein 5	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20160526	MGI			PMID:23935508
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20240523	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20250508	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0013520	increased CD4-positive NK T cell number		IEA		N	RGD:5509061	20230601	MGI			
1312867	Tppp3	tubulin polymerization-promoting protein family member 3	gene	MP:0013523	increased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20230601	MGI			
1312876	Tnfsf18	tumor necrosis factor (ligand) superfamily, member 18	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1312876	Tnfsf18	tumor necrosis factor (ligand) superfamily, member 18	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1312876	Tnfsf18	tumor necrosis factor (ligand) superfamily, member 18	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1312876	Tnfsf18	tumor necrosis factor (ligand) superfamily, member 18	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1312876	Tnfsf18	tumor necrosis factor (ligand) superfamily, member 18	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1312876	Tnfsf18	tumor necrosis factor (ligand) superfamily, member 18	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1312876	Tnfsf18	tumor necrosis factor (ligand) superfamily, member 18	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1312876	Tnfsf18	tumor necrosis factor (ligand) superfamily, member 18	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1312876	Tnfsf18	tumor necrosis factor (ligand) superfamily, member 18	gene	MP:0012243	decreased hepatoblast number		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0002673	abnormal sperm number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0005410	abnormal fertilization		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20170105	MGI			
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160225	MGI			PMID:25320092
1312878	Ube2j1	ubiquitin-conjugating enzyme E2J 1	gene	MP:0011941	increased fluid intake		IEA		N	RGD:5509061	20211021	MGI			
1312881	Smad6	SMAD family member 6	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20141003	MGI			
1312881	Smad6	SMAD family member 6	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1312881	Smad6	SMAD family member 6	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0003958	heart valve hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0006123	tricuspid valve atresia		IEA		N	RGD:5509061	20141003	MGI			
1312881	Smad6	SMAD family member 6	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1312881	Smad6	SMAD family member 6	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1312881	Smad6	SMAD family member 6	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0011665	d-loop transposition of the great arteries		IEA		N	RGD:5509061	20141003	MGI			
1312881	Smad6	SMAD family member 6	gene	MP:0031524	mitral valve hyperplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:10655064
1312881	Smad6	SMAD family member 6	gene	MP:0031529	pulmonary valve hyperplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:10655064
1312883	Golga7b	golgin A7B	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20260402	MGI			
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:25118264
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0002698	abnormal sclera morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0005098	abnormal optic choroid morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:25118264
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20161103	MGI			PMID:25118264
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0006187	retina deposits		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20240208	MGI			PMID:35230417
1312887	Cyp4v3	cytochrome P450, family 4, subfamily v, polypeptide 3	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:35230417
1312889	Trim69	tripartite motif-containing 69	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:33273151
1312889	Trim69	tripartite motif-containing 69	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210826	MGI			
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20200827	MGI			PMID:32646486
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20200827	MGI			PMID:32646486
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200820	MGI			PMID:32646486
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0009145	abnormal pancreatic acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0009154	pancreatic acinar hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0009162	absent pancreatic acinar cell zymogen granule		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0010600	enlarged pulmonary valve		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0010605	thick pulmonary valve cusps		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0010626	thick tricuspid valve cusps		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0010627	enlarged tricuspid valve		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218265
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0011945	increased eating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1312891	Rhbdf1	rhomboid 5 homolog 1	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:23969955
1312893	Cdc16	CDC16 cell division cycle 16	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22298771
1312896	Sulf2	sulfatase 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20250508	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20250508	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16901266
1312896	Sulf2	sulfatase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20250508	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16901266
1312896	Sulf2	sulfatase 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20210211	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16901266
1312896	Sulf2	sulfatase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16901266
1312896	Sulf2	sulfatase 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004545	enlarged esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0004548	dilated esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004687	split vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0004831	long incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16901266
1312896	Sulf2	sulfatase 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1312896	Sulf2	sulfatase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22298771
1312896	Sulf2	sulfatase 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1312896	Sulf2	sulfatase 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1312896	Sulf2	sulfatase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1312896	Sulf2	sulfatase 2	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:16901266
1312896	Sulf2	sulfatase 2	gene	MP:0012279	wide sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20180125	MGI			PMID:18213582
1312896	Sulf2	sulfatase 2	gene	MP:0031088	coughing		IAGP		N	RGD:5509061	20210211	MGI			PMID:17720696
1312898	Dse	dermatan sulfate epimerase	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19687302
1312898	Dse	dermatan sulfate epimerase	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19687302
1312898	Dse	dermatan sulfate epimerase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19687302
1312898	Dse	dermatan sulfate epimerase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19687302
1312898	Dse	dermatan sulfate epimerase	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1312898	Dse	dermatan sulfate epimerase	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19687302
1312898	Dse	dermatan sulfate epimerase	gene	MP:0003705	abnormal hypodermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19687302
1312898	Dse	dermatan sulfate epimerase	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1312898	Dse	dermatan sulfate epimerase	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19687302
1312898	Dse	dermatan sulfate epimerase	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19687302
1312898	Dse	dermatan sulfate epimerase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312900	Cdkl1	cyclin dependent kinase like 1	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20250508	MGI			
1312900	Cdkl1	cyclin dependent kinase like 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1312900	Cdkl1	cyclin dependent kinase like 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1312902	Aif1l	allograft inflammatory factor 1-like	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20160811	MGI			
1312902	Aif1l	allograft inflammatory factor 1-like	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20160811	MGI			
1312902	Aif1l	allograft inflammatory factor 1-like	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20160811	MGI			
1312902	Aif1l	allograft inflammatory factor 1-like	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20160811	MGI			
1312902	Aif1l	allograft inflammatory factor 1-like	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20160811	MGI			
1312902	Aif1l	allograft inflammatory factor 1-like	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1312902	Aif1l	allograft inflammatory factor 1-like	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20220811	MGI			
1312908	Matn3	matrilin 3	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1312908	Matn3	matrilin 3	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1312908	Matn3	matrilin 3	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877353
1312908	Matn3	matrilin 3	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877353
1312908	Matn3	matrilin 3	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1312908	Matn3	matrilin 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1312908	Matn3	matrilin 3	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877353
1312908	Matn3	matrilin 3	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1312908	Matn3	matrilin 3	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1312908	Matn3	matrilin 3	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1312908	Matn3	matrilin 3	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:17517694
1312908	Matn3	matrilin 3	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:17517694
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20201022	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20201022	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20201022	MGI			
1312910	Slc9b1	solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1312914	Prorp	protein only RNase P catalytic subunit	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20190919	MGI			PMID:27498866
1312914	Prorp	protein only RNase P catalytic subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190919	MGI			PMID:27498866
1312914	Prorp	protein only RNase P catalytic subunit	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20190919	MGI			PMID:27498866
1312914	Prorp	protein only RNase P catalytic subunit	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20190919	MGI			PMID:27498866
1312914	Prorp	protein only RNase P catalytic subunit	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20190919	MGI			PMID:27498866
1312914	Prorp	protein only RNase P catalytic subunit	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20190919	MGI			PMID:27498866
1312914	Prorp	protein only RNase P catalytic subunit	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20190919	MGI			PMID:27498866
1312914	Prorp	protein only RNase P catalytic subunit	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:27498866
1312915	Mnmip1	manchette microtubule inner protein 1	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240627	MGI			PMID:38835510
1312917	Msrb1	methionine sulfoxide reductase B1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22521563
1312917	Msrb1	methionine sulfoxide reductase B1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22521563
1312917	Msrb1	methionine sulfoxide reductase B1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18990697
1312917	Msrb1	methionine sulfoxide reductase B1	gene	MP:0012604	decreased glutathione level		IAGP		N	RGD:5509061	20260212	MGI			PMID:18990697
1312917	Msrb1	methionine sulfoxide reductase B1	gene	MP:0012605	decreased kidney glutathione level		IAGP		N	RGD:5509061	20260212	MGI			PMID:18990697
1312917	Msrb1	methionine sulfoxide reductase B1	gene	MP:0014867	increased malondialdehyde level		IAGP		N	RGD:5509061	20260212	MGI			PMID:18990697
1312917	Msrb1	methionine sulfoxide reductase B1	gene	MP:0014870	increased liver malondialdehyde level		IAGP		N	RGD:5509061	20260212	MGI			PMID:18990697
1312920	Mxd4	Max dimerization protein 4	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1312920	Mxd4	Max dimerization protein 4	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1312920	Mxd4	Max dimerization protein 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1312920	Mxd4	Max dimerization protein 4	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20230601	MGI			
1312923	Fbxo24	F-box protein 24	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20240613	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0014684	impaired spermiation		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:38470475
1312923	Fbxo24	F-box protein 24	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:39163107
1312923	Fbxo24	F-box protein 24	gene	MP:0031620	abnormal chromatoid body morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:38470475
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0004697	abnormal thyroid follicular cell morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0006350	increased circulating copper level		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0020365	increased brain iron level		IAGP		N	RGD:5509061	20180614	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0030593	abnormal manganese level		IAGP		N	RGD:5509061	20180621	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0030595	increased brain manganese level		IAGP		N	RGD:5509061	20180621	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0030598	increased liver manganese level		IAGP		N	RGD:5509061	20180621	MGI			PMID:28461334
1312928	Slc30a10	solute carrier family 30, member 10	gene	MP:0030601	increased circulating manganese level		IAGP		N	RGD:5509061	20180621	MGI			PMID:28461334
1312930	Rufy1	RUN and FYVE domain containing 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427635
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427635
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427635
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427635
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19766573
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427635
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427635
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427635
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427635
1312932	Lpar2	lysophosphatidic acid receptor 2	gene	MP:0010935	increased airway resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22427635
1312936	Scel	sciellin	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1312936	Scel	sciellin	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1312936	Scel	sciellin	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1312936	Scel	sciellin	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1312936	Scel	sciellin	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1312936	Scel	sciellin	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1312936	Scel	sciellin	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230601	MGI			
1312936	Scel	sciellin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16028229
1312936	Scel	sciellin	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20230601	MGI			
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244513
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244513
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244513
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244513
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244513
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244513
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244513
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244513
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20181227	MGI			
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0010099	abnormal thoracic cage shape		IEA		N	RGD:5509061	20181227	MGI			
1312938	Csmd1	CUB and Sushi multiple domains 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:24244513
1312940	Ankrd2	ankyrin repeat domain 2	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:24434510
1312940	Ankrd2	ankyrin repeat domain 2	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141225	MGI			PMID:24434510
1312940	Ankrd2	ankyrin repeat domain 2	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392382
1312940	Ankrd2	ankyrin repeat domain 2	gene	MP:0014920	increased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:17392382
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12910269
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0000676	abnormal body water content		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20190502	MGI			
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210520	MGI			
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20210520	MGI			
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12910269
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12910269
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12910269
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20211021	MGI			
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12910269
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12910269
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20160414	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0009935	abnormal Meibomian gland acinus morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0013116	focal hair loss in head/neck region		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0013375	abnormal sebocyte morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0014053	dry hair		IAGP		N	RGD:5509061	20160304	MGI			PMID:24636991
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:12910269
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:12910269
1312943	Cidea	cell death-inducing DNA fragmentation factor, alpha subunit-like effector A	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20180125	MGI			PMID:12910269
1312945	Srpk2	serine/arginine-rich protein specific kinase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1312945	Srpk2	serine/arginine-rich protein specific kinase 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1312945	Srpk2	serine/arginine-rich protein specific kinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1312945	Srpk2	serine/arginine-rich protein specific kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1312945	Srpk2	serine/arginine-rich protein specific kinase 2	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1312949	Sanbr	SANT and BTB domain regulator of CSR	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1312949	Sanbr	SANT and BTB domain regulator of CSR	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1312949	Sanbr	SANT and BTB domain regulator of CSR	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20250508	MGI			
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20210520	MGI			
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210826	MGI			
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221103	MGI			
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20221103	MGI			
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0004230	abnormal embryonic erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0011702	abnormal fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312951	Arhgef12	Rho guanine nucleotide exchange factor 12	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1312952	Tex2	testis expressed gene 2	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20200514	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20200514	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20231207	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1312952	Tex2	testis expressed gene 2	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0000450	absent snout		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20211021	MGI			
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0008736	micromelia		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20210826	MGI			
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0012522	abnormal stomodeum morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0012761	increased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0030202	nasal septum cartilage hypoplasia		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0030249	small frontonasal prominence		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0030342	small maxillary prominence		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0030344	absent maxillary prominence		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312954	Nubp2	nucleotide binding protein 2	gene	MP:0030346	small mandibular prominence		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0003547	abnormal pulmonary pressure		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0003822	decreased left ventricle systolic pressure		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0004009	abnormal diastolic filling velocity		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0004092	absent Z line		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0004093	diffuse Z line		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0004146	absent M line		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20160421	MGI			
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0010759	decreased right ventricle systolic pressure		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20170223	MGI			PMID:21177343
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0030564	thick myocardium compact layer		IAGP		N	RGD:5509061	20180524	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0030566	abnormal A band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0030567	abnormal I band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0030568	abnormal H zone morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26526197
1312963	Daam1	dishevelled associated activator of morphogenesis 1	gene	MP:0031613	fetal cardiomyocyte disarray		IAGP		N	RGD:5509061	20240321	MGI			PMID:21177343
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482943
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482943
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482943
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482943
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482943
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482943
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482943
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482943
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0009929	meningomyelocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:19482943
1312968	Itpk1	inositol 1,3,4-triphosphate 5/6 kinase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20150305	MGI			PMID:19482943
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0013329	abnormal preputial gland morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312970	Tbrg1	transforming growth factor beta regulated gene 1	gene	MP:0013538	increased Harderian gland adenoma incidence		IAGP		N	RGD:5509061	20160324	MGI			PMID:25393878
1312972	Cilp	cartilage intermediate layer protein, nucleotide pyrophosphohydrolase	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20201231	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20181227	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20170105	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20170105	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312974	Atl2	atlastin GTPase 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1312976	Kif21a	kinesin family member 21A	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0001070	abnormal abducens nerve morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1312976	Kif21a	kinesin family member 21A	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0005247	abnormal extraocular muscle morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312976	Kif21a	kinesin family member 21A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312976	Kif21a	kinesin family member 21A	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20200402	MGI			
1312976	Kif21a	kinesin family member 21A	gene	MP:0013827	thin oculomotor nerve		IAGP		N	RGD:5509061	20181122	MGI			PMID:24656932
1312979	Polg2	polymerase (DNA directed), gamma 2, accessory subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197651
1312979	Polg2	polymerase (DNA directed), gamma 2, accessory subunit	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20191114	MGI			PMID:30395686
1312979	Polg2	polymerase (DNA directed), gamma 2, accessory subunit	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197651
1312979	Polg2	polymerase (DNA directed), gamma 2, accessory subunit	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197651
1312979	Polg2	polymerase (DNA directed), gamma 2, accessory subunit	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197651
1312979	Polg2	polymerase (DNA directed), gamma 2, accessory subunit	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197651
1312979	Polg2	polymerase (DNA directed), gamma 2, accessory subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312979	Polg2	polymerase (DNA directed), gamma 2, accessory subunit	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197651
1312979	Polg2	polymerase (DNA directed), gamma 2, accessory subunit	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197651
1312981	Mamdc2	MAM domain containing 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1312985	Twf2	twinfilin actin binding protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21876732
1312989	Slc25a28	solute carrier family 25, member 28	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
1312989	Slc25a28	solute carrier family 25, member 28	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210415	MGI			PMID:32518166
1312989	Slc25a28	solute carrier family 25, member 28	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210415	MGI			PMID:32518166
1312989	Slc25a28	solute carrier family 25, member 28	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210415	MGI			PMID:32518166
1312989	Slc25a28	solute carrier family 25, member 28	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20210415	MGI			PMID:32518166
1312989	Slc25a28	solute carrier family 25, member 28	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20210415	MGI			PMID:32518166
1312989	Slc25a28	solute carrier family 25, member 28	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32518166
1312997	Zfp281	zinc finger protein 281	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1312997	Zfp281	zinc finger protein 281	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20201022	MGI			
1312997	Zfp281	zinc finger protein 281	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20231207	MGI			
1312997	Zfp281	zinc finger protein 281	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1312997	Zfp281	zinc finger protein 281	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1312997	Zfp281	zinc finger protein 281	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20241121	MGI			
1312997	Zfp281	zinc finger protein 281	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21915945
1312997	Zfp281	zinc finger protein 281	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21915945
1312997	Zfp281	zinc finger protein 281	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1312997	Zfp281	zinc finger protein 281	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550782
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550782
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550782
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0003364	increased insulinoma incidence		IAGP		N	RGD:5509061	20170406	MGI			PMID:18846252
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20170406	MGI			PMID:18846252
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550782
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550782
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20150611	MGI			PMID:17550782
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550782
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060135
1313004	Rps6kb2	ribosomal protein S6 kinase B2	gene	MP:0014173	increased fatty acid beta-oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:17550782
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20181227	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1313005	Nars2	asparaginyl-tRNA synthetase 2 (mitochondrial)(putative)	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1313007	Pcnx4	pecanex homolog 4	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1313007	Pcnx4	pecanex homolog 4	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913445
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322176
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796634
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913445
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796634
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322176
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796634
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322176
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0006412	abnormal T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796634
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14607906
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796634
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913445
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796634
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913445
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913445
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796634
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913445
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008363	decreased CD8-positive, gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913445
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322176
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777964
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14607906
1313010	Il15ra	interleukin 15 receptor, alpha chain	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913445
1313013	B3gnt3	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3	gene	MP:0003998	decreased thermal nociceptive threshold		IEA		N	RGD:5509061	20111116	MGI			
1313015	Itga10	integrin, alpha 10	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713743
1313015	Itga10	integrin, alpha 10	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713743
1313015	Itga10	integrin, alpha 10	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713743
1313015	Itga10	integrin, alpha 10	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713743
1313015	Itga10	integrin, alpha 10	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713743
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20220519	MGI			
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210826	MGI			
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20220519	MGI			
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20220519	MGI			
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20230202	MGI			PMID:36539599
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0004357	long tibia		IAGP		N	RGD:5509061	20230202	MGI			PMID:36539599
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20230202	MGI			PMID:36539599
1313019	Adamtsl3	ADAMTS-like 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1313021	Gask1a	golgi associated kinase 1A	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1313026	Atpaf2	ATP synthase mitochondrial F1 complex assembly factor 2	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20141003	MGI			
1313026	Atpaf2	ATP synthase mitochondrial F1 complex assembly factor 2	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20160804	MGI			
1313026	Atpaf2	ATP synthase mitochondrial F1 complex assembly factor 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1313026	Atpaf2	ATP synthase mitochondrial F1 complex assembly factor 2	gene	MP:0003345	decreased rib number		IEA		N	RGD:5509061	20160804	MGI			
1313026	Atpaf2	ATP synthase mitochondrial F1 complex assembly factor 2	gene	MP:0004648	decreased thoracic vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1313026	Atpaf2	ATP synthase mitochondrial F1 complex assembly factor 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250410	MGI			PMID:34375736
1313026	Atpaf2	ATP synthase mitochondrial F1 complex assembly factor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313034	Tctn3	tectonic family member 3	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1313034	Tctn3	tectonic family member 3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313034	Tctn3	tectonic family member 3	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313034	Tctn3	tectonic family member 3	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1313034	Tctn3	tectonic family member 3	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1313034	Tctn3	tectonic family member 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1313034	Tctn3	tectonic family member 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313034	Tctn3	tectonic family member 3	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20201022	MGI			
1313034	Tctn3	tectonic family member 3	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313034	Tctn3	tectonic family member 3	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313034	Tctn3	tectonic family member 3	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20220811	MGI			
1313034	Tctn3	tectonic family member 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1313034	Tctn3	tectonic family member 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313034	Tctn3	tectonic family member 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313034	Tctn3	tectonic family member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313034	Tctn3	tectonic family member 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313034	Tctn3	tectonic family member 3	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313034	Tctn3	tectonic family member 3	gene	MP:0013214	decreased embryonic neuroepithelium primary cilium number		IAGP		N	RGD:5509061	20191003	MGI			PMID:28800946
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210826	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20220811	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20241121	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20210826	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20241121	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20210826	MGI			
1313035	Fsd2	fibronectin type III and SPRY domain containing 2	gene	MP:0010571	shortened ST segment		IEA		N	RGD:5509061	20241121	MGI			
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011243	decreased fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0011913	abnormal reticulocyte cell number		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20170907	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:26456157
1313037	Mcm3	minichromosome maintenance complex component 3	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:26456157
1313039	Pank2	pantothenate kinase 2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20231207	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20231207	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20231207	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20231207	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20231207	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20231207	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0002638	abnormal pupillary reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20231207	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0008455	abnormal retina rod cell inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525657
1313039	Pank2	pantothenate kinase 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20231207	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:22815849
1313039	Pank2	pantothenate kinase 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1313039	Pank2	pantothenate kinase 2	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:15525657
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20151126	MGI			PMID:24771530
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20151126	MGI			PMID:24771530
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20170511	MGI			PMID:27780844
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151203	MGI			PMID:24771530
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20170511	MGI			PMID:27780844
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20151126	MGI			PMID:24771530
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20151126	MGI			PMID:24771530
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364144
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0011724	ectopic cortical neuron		IAGP		N	RGD:5509061	20170511	MGI			PMID:27780844
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20170511	MGI			PMID:27780844
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20170511	MGI			PMID:27780844
1313048	Magoh	mago homolog, exon junction complex core component	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20170511	MGI			PMID:27780844
1313049	Dcaf1	DDB1 and CUL4 associated factor 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606781
1313049	Dcaf1	DDB1 and CUL4 associated factor 1	gene	MP:0006204	embryonic lethality before implantation		IEA		N	RGD:5509061	20111116	MGI			
1313049	Dcaf1	DDB1 and CUL4 associated factor 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606781
1313049	Dcaf1	DDB1 and CUL4 associated factor 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20150212	MGI			PMID:18606781
1313049	Dcaf1	DDB1 and CUL4 associated factor 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:18606781
1313050	Lctl	lactase-like	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:29425878
1313050	Lctl	lactase-like	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170406	MGI			
1313050	Lctl	lactase-like	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20190207	MGI			PMID:29425878
1313050	Lctl	lactase-like	gene	MP:0010255	cortical cataract		IAGP		N	RGD:5509061	20190207	MGI			PMID:29425878
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313053	N4bp1	NEDD4 binding protein 1	gene	MP:0013022	increased Ly6C high monocyte number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32971525
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0004708	short lumbar vertebrae		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313055	Pbxip1	pre B cell leukemia transcription factor interacting protein 1	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20191024	MGI			PMID:30659184
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001400	hyperresponsive		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:28429368
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20180809	MGI			PMID:28429368
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180809	MGI			PMID:15987682
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180809	MGI			PMID:28429368
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0030585	enhanced behavioral response to amphetamine		IAGP		N	RGD:5509061	20180809	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0030635	increased taurine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:28429368
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:23216354
1313057	Slc25a12	solute carrier family 25 (mitochondrial carrier, Aralar), member 12	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:23216354
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578028
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0003092	decreased cornea stroma thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0003092	decreased cornea stroma thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578028
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0004284	abnormal Descemet membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0004284	abnormal Descemet membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002996
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0004284	abnormal Descemet membrane morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:23422828
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578028
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002996
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:23422828
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578028
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578028
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002996
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002996
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20161013	MGI			PMID:23422828
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:23422828
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0009829	enlarged eye anterior chamber		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578028
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0031177	decreased Descemet membrane thickness		IAGP		N	RGD:5509061	20201119	MGI			PMID:16051690
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0031177	decreased Descemet membrane thickness		IAGP		N	RGD:5509061	20201119	MGI			PMID:19578028
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:16051690
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0031688	dilated rough endoplasmic reticulum		IAGP		N	RGD:5509061	20251120	MGI			PMID:22002996
1313059	Col8a2	collagen, type VIII, alpha 2	gene	MP:0031688	dilated rough endoplasmic reticulum		IAGP		N	RGD:5509061	20251120	MGI			PMID:23422828
1313061	Cep76	centrosomal protein 76	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20161201	MGI			
1313061	Cep76	centrosomal protein 76	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1313061	Cep76	centrosomal protein 76	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20230119	MGI			PMID:35962060
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20230119	MGI			PMID:35962060
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20230119	MGI			PMID:35962060
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20230119	MGI			PMID:35962060
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20230119	MGI			PMID:35962060
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230119	MGI			PMID:35962060
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0012051	spasticity		IAGP		N	RGD:5509061	20230119	MGI			PMID:35962060
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20230119	MGI			PMID:35962060
1313065	Ubap1	ubiquitin-associated protein 1	gene	MP:0031204	hindlimb paresis		IAGP		N	RGD:5509061	20230119	MGI			PMID:35962060
1313073	Kifap3	kinesin-associated protein 3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834408
1313073	Kifap3	kinesin-associated protein 3	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834408
1313073	Kifap3	kinesin-associated protein 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834408
1313073	Kifap3	kinesin-associated protein 3	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834408
1313073	Kifap3	kinesin-associated protein 3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834408
1313073	Kifap3	kinesin-associated protein 3	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834408
1313073	Kifap3	kinesin-associated protein 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1313073	Kifap3	kinesin-associated protein 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834408
1313073	Kifap3	kinesin-associated protein 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313075	Sema7a	sema domain, immunoglobulin domain (Ig), and GPI membrane anchor, (semaphorin) 7A	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879062
1313075	Sema7a	sema domain, immunoglobulin domain (Ig), and GPI membrane anchor, (semaphorin) 7A	gene	MP:0005237	abnormal olfactory tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879062
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000314	schistocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000314	schistocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000422	delayed hair appearance		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11154235
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11154235
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001386	abnormal maternal nurturing		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20200514	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11154235
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001923	reduced female fertility		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002082	postnatal lethality		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002095	abnormal skin pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002161	abnormal fertility/fecundity		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002397	abnormal bone marrow morphology		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6234993
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10772878
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6234993
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002704	tubular nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002810	microcytic anemia		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10772878
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002830	gallstones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11154235
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492791
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0003657	abnormal erythrocyte osmotic lysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0003868	abnormal feces composition		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0003946	renal necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11154235
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005096	erythroblastosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008388	hypochromic microcytic anemia		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:1934076
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0008956	decreased cellular hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0009547	elliptocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10772878
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0009547	elliptocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11154235
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0009547	elliptocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0009568	abnormal red blood cell deformability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393645
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0010035	increased erythrocyte clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0010163	hemolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20056793
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0010922	alveolitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011085	postnatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011188	increased erythrocyte protoporphyrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011188	increased erythrocyte protoporphyrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:658175
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0011188	increased erythrocyte protoporphyrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0014473	increased pulmonary alveolus wall thickness		IAGP		N	RGD:5509061	20240704	MGI			PMID:8355480
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0014605	dark liver		IAGP		N	RGD:5509061	20250206	MGI			PMID:14451913
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0014606	dark spleen		IAGP		N	RGD:5509061	20250206	MGI			PMID:6841965
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0014990	enhanced erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:7059672
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:10772878
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0021003	cerebral infarct		IAGP		N	RGD:5509061	20210805	MGI			PMID:9373273
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:6763106
1313078	Spta1	spectrin alpha, erythrocytic 1	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:6841965
1313082	Jph2	junctophilin 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949023
1313082	Jph2	junctophilin 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949023
1313082	Jph2	junctophilin 2	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949023
1313082	Jph2	junctophilin 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10949023
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694879
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12853434
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23319618
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:21659555
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:21659555
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:21659555
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694879
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:21659555
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694879
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813673
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694879
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813673
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23319618
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11694879
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23319618
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:21659555
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813673
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23319618
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20161124	MGI			PMID:21659555
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180201	MGI			PMID:26247368
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:26247368
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008445	increased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813673
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008445	increased retina cone cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:21659555
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:30228185
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20161124	MGI			PMID:21659555
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008454	absent retina rod cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813673
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20180201	MGI			PMID:26247368
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21813673
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20180201	MGI			PMID:26247368
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0014645	decreased optokinetic reflex		IAGP		N	RGD:5509061	20250306	MGI			PMID:26247368
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0014658	absent a-wave		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1313084	Nrl	neural retina leucine zipper gene	gene	MP:0020439	absent b-wave		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1313090	Ccm2l	cerebral cavernous malformation 2-like	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:22898778
1313092	Bag1	BCL2-associated athanogene 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15560850
1313092	Bag1	BCL2-associated athanogene 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1313092	Bag1	BCL2-associated athanogene 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1313092	Bag1	BCL2-associated athanogene 1	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15560850
1313092	Bag1	BCL2-associated athanogene 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15560850
1313096	Ipo4	importin 4	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210128	MGI			
1313096	Ipo4	importin 4	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1313096	Ipo4	importin 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313100	Ldlrad4	low density lipoprotein receptor class A domain containing 4	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20201231	MGI			
1313100	Ldlrad4	low density lipoprotein receptor class A domain containing 4	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20241121	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1313102	Lipt2	lipoyl(octanoyl) transferase 2 (putative)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20241121	MGI			
1313104	Poli	polymerase (DNA directed), iota	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015482
1313104	Poli	polymerase (DNA directed), iota	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824086
1313104	Poli	polymerase (DNA directed), iota	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955086
1313104	Poli	polymerase (DNA directed), iota	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955086
1313104	Poli	polymerase (DNA directed), iota	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
1313106	Pnn	pinin	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19892877
1313106	Pnn	pinin	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19892877
1313106	Pnn	pinin	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19892877
1313106	Pnn	pinin	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:19892877
1313106	Pnn	pinin	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19892877
1313106	Pnn	pinin	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0010378	increased respiratory quotient		IEA		N	RGD:5509061	20250508	MGI			
1313106	Pnn	pinin	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17654715
1313106	Pnn	pinin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160211	MGI			
1313106	Pnn	pinin	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313106	Pnn	pinin	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20221215	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1313109	Usb1	U6 snRNA biogenesis 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1313111	Sirt6	sirtuin 6	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816089
1313111	Sirt6	sirtuin 6	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20160310	MGI			PMID:26629408
1313111	Sirt6	sirtuin 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160310	MGI			PMID:26629408
1313111	Sirt6	sirtuin 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0001316	cornea scarring		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816089
1313111	Sirt6	sirtuin 6	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816089
1313111	Sirt6	sirtuin 6	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1313111	Sirt6	sirtuin 6	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816089
1313111	Sirt6	sirtuin 6	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1313111	Sirt6	sirtuin 6	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0008402	increased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0008737	abnormal spleen physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0020860	abnormal cornea physiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:28448551
1313111	Sirt6	sirtuin 6	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:16439206
1313111	Sirt6	sirtuin 6	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:20847051
1313111	Sirt6	sirtuin 6	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:28448551
1313113	Foxb1	forkhead box B1	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11170346
1313113	Foxb1	forkhead box B1	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654859
1313113	Foxb1	forkhead box B1	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0000867	abnormal cerebellum anterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118797
1313113	Foxb1	forkhead box B1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118797
1313113	Foxb1	forkhead box B1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136764
1313113	Foxb1	forkhead box B1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136764
1313113	Foxb1	forkhead box B1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136764
1313113	Foxb1	forkhead box B1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136764
1313113	Foxb1	forkhead box B1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654859
1313113	Foxb1	forkhead box B1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118797
1313113	Foxb1	forkhead box B1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136764
1313113	Foxb1	forkhead box B1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118797
1313113	Foxb1	forkhead box B1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136764
1313113	Foxb1	forkhead box B1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10662642
1313113	Foxb1	forkhead box B1	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118797
1313113	Foxb1	forkhead box B1	gene	MP:0004162	abnormal mammillary body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11170346
1313113	Foxb1	forkhead box B1	gene	MP:0004162	abnormal mammillary body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654859
1313113	Foxb1	forkhead box B1	gene	MP:0004162	abnormal mammillary body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:15654859
1313113	Foxb1	forkhead box B1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118797
1313113	Foxb1	forkhead box B1	gene	MP:0009038	decreased inferior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11170346
1313113	Foxb1	forkhead box B1	gene	MP:0009038	decreased inferior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11170346
1313113	Foxb1	forkhead box B1	gene	MP:0009505	abnormal mammary gland lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11170346
1313113	Foxb1	forkhead box B1	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11170346
1313113	Foxb1	forkhead box B1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136764
1313113	Foxb1	forkhead box B1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118797
1313113	Foxb1	forkhead box B1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136764
1313113	Foxb1	forkhead box B1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9118797
1313113	Foxb1	forkhead box B1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409663
1313113	Foxb1	forkhead box B1	gene	MP:0013718	galactostasis		IAGP		N	RGD:5509061	20150409	MGI			PMID:11170346
1313113	Foxb1	forkhead box B1	gene	MP:0013718	galactostasis		IAGP		N	RGD:5509061	20150409	MGI			PMID:9118797
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220407	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0009362	abnormal primary ovarian follicle morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0013539	increased ovary adenoma incidence		IAGP		N	RGD:5509061	20150219	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:22771120
1313115	Mcm8	minichromosome maintenance 8 homologous recombination repair factor	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:22771120
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20221215	MGI			
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20221215	MGI			
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20221215	MGI			
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20221215	MGI			
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20221215	MGI			
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0013210	abnormal primary cilium physiology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0013213	abnormal embryonic neuroepithelium primary cilium morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313117	Cdk20	cyclin dependent kinase 20	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344982
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313119	Ppm1l	protein phosphatase 1 (formerly 2C)-like	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20180308	MGI			PMID:27680501
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0008175	absent follicular B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0009145	abnormal pancreatic acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0009154	pancreatic acinar hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548465
1313121	Pgm3	phosphoglucomutase 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1313125	Sln	sarcolipin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200514	MGI			PMID:31833196
1313125	Sln	sarcolipin	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200514	MGI			PMID:31833196
1313125	Sln	sarcolipin	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17971438
1313125	Sln	sarcolipin	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0009121	increased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313125	Sln	sarcolipin	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20180111	MGI			PMID:22961106
1313126	Ccdc174	coiled-coil domain containing 174	gene	MP:0006205	embryonic lethality between implantation and somite formation		IEA		N	RGD:5509061	20141003	MGI			
1313126	Ccdc174	coiled-coil domain containing 174	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313126	Ccdc174	coiled-coil domain containing 174	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0008409	increased cellular sensitivity to hydroxyurea induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313127	Kmt5c	lysine methyltransferase 5C	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1313129	Smc2	structural maintenance of chromosomes 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:25474630
1313129	Smc2	structural maintenance of chromosomes 2	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:25474630
1313129	Smc2	structural maintenance of chromosomes 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20160204	MGI			PMID:25474630
1313129	Smc2	structural maintenance of chromosomes 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20160204	MGI			PMID:25474630
1313129	Smc2	structural maintenance of chromosomes 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20160204	MGI			PMID:25474630
1313129	Smc2	structural maintenance of chromosomes 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160204	MGI			PMID:25474630
1313129	Smc2	structural maintenance of chromosomes 2	gene	MP:0012203	abnormal neuronal stem cell morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:25474630
1313129	Smc2	structural maintenance of chromosomes 2	gene	MP:0012204	abnormal neuronal stem cell physiology		IAGP		N	RGD:5509061	20160204	MGI			PMID:25474630
1313131	Phf2	PHD finger protein 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0009131	decreased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313131	Phf2	PHD finger protein 2	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274892
1313133	Frmpd1	FERM and PDZ domain containing 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1313133	Frmpd1	FERM and PDZ domain containing 1	gene	MP:0000556	abnormal hindlimb morphology		IEA		N	RGD:5509061	20240523	MGI			
1313133	Frmpd1	FERM and PDZ domain containing 1	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20240523	MGI			
1313133	Frmpd1	FERM and PDZ domain containing 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1313135	Reep1	receptor accessory protein 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20150730	MGI			PMID:24051375
1313135	Reep1	receptor accessory protein 1	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051375
1313135	Reep1	receptor accessory protein 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051375
1313135	Reep1	receptor accessory protein 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051375
1313135	Reep1	receptor accessory protein 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051375
1313135	Reep1	receptor accessory protein 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0005248	abnormal Harderian gland morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051375
1313135	Reep1	receptor accessory protein 1	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0009122	decreased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0010946	hyperpnea		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0012051	spasticity		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0012051	spasticity		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0020211	slow movement		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313135	Reep1	receptor accessory protein 1	gene	MP:0030736	increased glutamic acid level		IAGP		N	RGD:5509061	20181004	MGI			PMID:27638887
1313135	Reep1	receptor accessory protein 1	gene	MP:0031204	hindlimb paresis		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0002965	increased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0003896	prolonged PR interval		IEA		N	RGD:5509061	20260402	MGI			
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20250508	MGI			
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313139	Slc5a10	solute carrier family 5 (sodium/glucose cotransporter), member 10	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451068
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22875804
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230601	MGI			
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20160128	MGI			PMID:24567532
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22875804
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22875804
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20160128	MGI			PMID:24567532
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22875804
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0010677	decreased activation-induced cell death of T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22875804
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:22875804
1313141	Havcr2	hepatitis A virus cellular receptor 2	gene	MP:0031045	decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:22875804
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20201022	MGI			
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20201022	MGI			
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210826	MGI			
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210826	MGI			
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20201224	MGI			PMID:30591559
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20201224	MGI			PMID:30591559
1313143	Ythdf3	YTH N6-methyladenosine RNA binding protein 3	gene	MP:0031023	decreased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20201224	MGI			PMID:30591559
1313147	Psmd13	proteasome (prosome, macropain) 26S subunit, non-ATPase, 13	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313147	Psmd13	proteasome (prosome, macropain) 26S subunit, non-ATPase, 13	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20250605	MGI			PMID:40123200
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20250508	MGI			
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20250605	MGI			PMID:40123200
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20250605	MGI			PMID:40123200
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20250605	MGI			PMID:40123200
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20250605	MGI			PMID:40123200
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20250605	MGI			PMID:40123200
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20250605	MGI			PMID:40123200
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20250605	MGI			PMID:40123200
1313149	Tatdn1	TatD DNase domain containing 1	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20250605	MGI			PMID:40123200
1313151	Trim32	tripartite motif-containing 32	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22299041
1313151	Trim32	tripartite motif-containing 32	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775502
1313151	Trim32	tripartite motif-containing 32	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22299041
1313151	Trim32	tripartite motif-containing 32	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775502
1313151	Trim32	tripartite motif-containing 32	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22299041
1313151	Trim32	tripartite motif-containing 32	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22299041
1313151	Trim32	tripartite motif-containing 32	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775502
1313151	Trim32	tripartite motif-containing 32	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22299041
1313151	Trim32	tripartite motif-containing 32	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775502
1313151	Trim32	tripartite motif-containing 32	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:22299041
1313151	Trim32	tripartite motif-containing 32	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155210
1313151	Trim32	tripartite motif-containing 32	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775502
1313151	Trim32	tripartite motif-containing 32	gene	MP:0031328	delayed skeletal muscle regeneration		IAGP		N	RGD:5509061	20220106	MGI			PMID:22299041
1313156	Zkscan7	zinc finger with KRAB and SCAN domains 7	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1313156	Zkscan7	zinc finger with KRAB and SCAN domains 7	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1313156	Zkscan7	zinc finger with KRAB and SCAN domains 7	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1313156	Zkscan7	zinc finger with KRAB and SCAN domains 7	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1313156	Zkscan7	zinc finger with KRAB and SCAN domains 7	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1313156	Zkscan7	zinc finger with KRAB and SCAN domains 7	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1313159	Plekha3	pleckstrin homology domain containing A3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1313159	Plekha3	pleckstrin homology domain containing A3	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20181227	MGI			
1313161	Fam171a1	family with sequence similarity 171, member A1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1313163	Abhd17b	abhydrolase domain containing 17B	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210128	MGI			
1313163	Abhd17b	abhydrolase domain containing 17B	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210128	MGI			
1313163	Abhd17b	abhydrolase domain containing 17B	gene	MP:0002546	mydriasis		IEA		N	RGD:5509061	20210128	MGI			
1313163	Abhd17b	abhydrolase domain containing 17B	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1313168	Snrpe	small nuclear ribonucleoprotein E	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258617
1313168	Snrpe	small nuclear ribonucleoprotein E	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258617
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0010664	abnormal vitelline artery morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313170	Pdzrn3	PDZ domain containing RING finger 3	gene	MP:0011521	decreased placental labyrinth size		IAGP		N	RGD:5509061	20160310	MGI			PMID:25198863
1313177	Tbc1d30	TBC1 domain family, member 30	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1313177	Tbc1d30	TBC1 domain family, member 30	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20181227	MGI			
1313177	Tbc1d30	TBC1 domain family, member 30	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1313177	Tbc1d30	TBC1 domain family, member 30	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1313177	Tbc1d30	TBC1 domain family, member 30	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20210826	MGI			
1313177	Tbc1d30	TBC1 domain family, member 30	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210826	MGI			
1313179	Lrrn4	leucine rich repeat neuronal 4	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870286
1313179	Lrrn4	leucine rich repeat neuronal 4	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870286
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642395
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642395
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642395
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642395
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642395
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642395
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642395
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642395
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0004835	abnormal miniature endplate potential		IEA		N	RGD:5509061	20111116	MGI			
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2917690
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0009684	abnormal spinal cord lateral motor column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8642395
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0010387	abnormal Bergmann glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18337413
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:19625515
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0011730	increased myelin sheath thickness		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0012023	decreased melanocyte number		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0014331	abnormal Purkinje cell mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:23041622
1313184	Afg3l2	AFG3-like AAA ATPase 2	gene	MP:0014345	abnormal neuron mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:19625515
1313186	Cyp4f18	cytochrome P450, family 4, subfamily f, polypeptide 18	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:24632148
1313186	Cyp4f18	cytochrome P450, family 4, subfamily f, polypeptide 18	gene	MP:0009817	decreased leukotriene level		IAGP		N	RGD:5509061	20170314	MGI			PMID:24632148
1313186	Cyp4f18	cytochrome P450, family 4, subfamily f, polypeptide 18	gene	MP:0010953	abnormal fatty acid oxidation		IAGP		N	RGD:5509061	20170314	MGI			PMID:24632148
1313188	Golga3	golgin A3	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892724
1313188	Golga3	golgin A3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892724
1313188	Golga3	golgin A3	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0002686	globozoospermia		IEA		N	RGD:5509061	20141003	MGI			
1313188	Golga3	golgin A3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892724
1313188	Golga3	golgin A3	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1313188	Golga3	golgin A3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1313188	Golga3	golgin A3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160421	MGI			
1313188	Golga3	golgin A3	gene	MP:0004852	decreased testis weight		IEA		N	RGD:5509061	20141003	MGI			
1313188	Golga3	golgin A3	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20160421	MGI			
1313188	Golga3	golgin A3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1313188	Golga3	golgin A3	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0008545	absent sperm flagellum		IEA		N	RGD:5509061	20141003	MGI			
1313188	Golga3	golgin A3	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313188	Golga3	golgin A3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892724
1313188	Golga3	golgin A3	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23495255
1313193	Phf10	PHD finger protein 10	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1313193	Phf10	PHD finger protein 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16716191
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0011622	abnormal habituation to a novel odor		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0012315	impaired learning		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20161229	MGI			PMID:26979507
1313195	Arhgap32	Rho GTPase activating protein 32	gene	MP:0021117	abnormal huddling behavior		IAGP		N	RGD:5509061	20220519	MGI			PMID:26979507
1313197	Amotl1	angiomotin-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190516	MGI			PMID:30375152
1313197	Amotl1	angiomotin-like 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20210729	MGI			PMID:27464479
1313197	Amotl1	angiomotin-like 1	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20210729	MGI			PMID:27464479
1313197	Amotl1	angiomotin-like 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20210729	MGI			PMID:27464479
1313197	Amotl1	angiomotin-like 1	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20210729	MGI			PMID:27464479
1313197	Amotl1	angiomotin-like 1	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20210729	MGI			PMID:27464479
1313197	Amotl1	angiomotin-like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190516	MGI			PMID:30375152
1313197	Amotl1	angiomotin-like 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190516	MGI			PMID:30375152
1313197	Amotl1	angiomotin-like 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190516	MGI			PMID:30375152
1313198	Limch1	LIM and calponin homology domains 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20240307	MGI			PMID:36977593
1313198	Limch1	LIM and calponin homology domains 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1313198	Limch1	LIM and calponin homology domains 1	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20240307	MGI			PMID:36977593
1313198	Limch1	LIM and calponin homology domains 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:36977593
1313198	Limch1	LIM and calponin homology domains 1	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20240307	MGI			PMID:36977593
1313198	Limch1	LIM and calponin homology domains 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20240307	MGI			PMID:36977593
1313198	Limch1	LIM and calponin homology domains 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20240307	MGI			PMID:36977593
1313198	Limch1	LIM and calponin homology domains 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313198	Limch1	LIM and calponin homology domains 1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20211021	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20241121	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230119	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20230119	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20240523	MGI			
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313200	Topors	topoisomerase I binding, arginine/serine-rich	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20240808	MGI			PMID:20429939
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20240118	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16317048
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0010496	abnormal pectinate muscle morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0020135	abnormal heart ventricle wall thickness		IAGP		N	RGD:5509061	20240118	MGI			PMID:19652092
1313205	Lims2	LIM and senescent cell antigen like domains 2	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231102	MGI			PMID:19652092
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000158	absent sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210520	MGI			
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572674
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572674
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20171214	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001349	excessive tearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210520	MGI			
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20221215	MGI			
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0002982	abnormal primordial germ cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210826	MGI			
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003856	abnormal hindlimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003856	abnormal hindlimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20171214	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004472	broad nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004652	small caudal vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004657	small sacral vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004667	vertebral body hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004708	short lumbar vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0005222	abnormal somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572674
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0006165	entropion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0006212	large orbits		IAGP		N	RGD:5509061	20170928	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0008391	abnormal primordial germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0008786	abnormal hindgut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0009284	abnormal sympathetic neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0009575	abnormal pubic symphysis morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:11713269
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0009666	abnormal embryo attachment		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572674
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22216013
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353862
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700181
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0011772	genital tubercle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0012062	small tail bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20171214	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0014106	delayed chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:10651906
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0014106	delayed chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0030321	abnormal tegmen tympani morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:14745966
1313208	Ror2	receptor tyrosine kinase-like orphan receptor 2	gene	MP:0030935	increased primordial germ cell apoptosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:22216013
1313213	Adam33	a disintegrin and metallopeptidase domain 33	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1313213	Adam33	a disintegrin and metallopeptidase domain 33	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943435
1313213	Adam33	a disintegrin and metallopeptidase domain 33	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1313213	Adam33	a disintegrin and metallopeptidase domain 33	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1313215	Cherp	calcium homeostasis endoplasmic reticulum protein	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210826	MGI			
1313215	Cherp	calcium homeostasis endoplasmic reticulum protein	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240926	MGI			
1313215	Cherp	calcium homeostasis endoplasmic reticulum protein	gene	MP:0002718	abnormal inner cell mass morphology		IEA		N	RGD:5509061	20240926	MGI			
1313215	Cherp	calcium homeostasis endoplasmic reticulum protein	gene	MP:0005028	abnormal trophectoderm morphology		IEA		N	RGD:5509061	20240926	MGI			
1313215	Cherp	calcium homeostasis endoplasmic reticulum protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313215	Cherp	calcium homeostasis endoplasmic reticulum protein	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20240926	MGI			
1313215	Cherp	calcium homeostasis endoplasmic reticulum protein	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1313215	Cherp	calcium homeostasis endoplasmic reticulum protein	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1313217	Dazap1	DAZ associated protein 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1313217	Dazap1	DAZ associated protein 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1313217	Dazap1	DAZ associated protein 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1313217	Dazap1	DAZ associated protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1313217	Dazap1	DAZ associated protein 1	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669443
1313217	Dazap1	DAZ associated protein 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:18669443
1313219	Slc72a1	solute carrier family 71 member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160505	MGI			PMID:27107036
1313219	Slc72a1	solute carrier family 71 member 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160505	MGI			PMID:27107036
1313219	Slc72a1	solute carrier family 71 member 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20160505	MGI			PMID:27107036
1313219	Slc72a1	solute carrier family 71 member 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20160505	MGI			PMID:27107036
1313219	Slc72a1	solute carrier family 71 member 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20160505	MGI			PMID:27107036
1313219	Slc72a1	solute carrier family 71 member 1	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20160505	MGI			PMID:27107036
1313219	Slc72a1	solute carrier family 71 member 1	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20160505	MGI			PMID:27107036
1313219	Slc72a1	solute carrier family 71 member 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20160505	MGI			PMID:27107036
1313219	Slc72a1	solute carrier family 71 member 1	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20160505	MGI			PMID:27107036
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0000119	abnormal tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497272
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17569887
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18208976
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17569887
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811150
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17569887
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497272
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497272
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497272
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811150
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497272
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18190787
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003930	abnormal tooth hard tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0003930	abnormal tooth hard tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16497272
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0004674	thin ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:17569887
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20211021	MGI			
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811150
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0009070	small oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18208976
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20201231	MGI			
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:17569887
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:23505553
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0030132	periodontium inflammation		IAGP		N	RGD:5509061	20171005	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0030451	abnormal dentin mineralization		IAGP		N	RGD:5509061	20180215	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0030494	abnormal molar root morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:16314533
1313224	Postn	periostin, osteoblast specific factor	gene	MP:0030524	abnormal tooth root resorption		IAGP		N	RGD:5509061	20180118	MGI			PMID:16314533
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20200514	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20200514	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220519	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:15606491
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15606491
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15606491
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15606491
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15606491
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220519	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15606491
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15606491
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0013319	seminal vesicle atrophy		IAGP		N	RGD:5509061	20141204	MGI			PMID:15606491
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20210128	MGI			
1313226	Plag1	pleiomorphic adenoma gene 1	gene	MP:0031362	decreased prostate gland ventral lobe weight		IAGP		N	RGD:5509061	20220303	MGI			PMID:15606491
1313229	Haus4	HAUS augmin-like complex, subunit 4	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240919	MGI			
1313229	Haus4	HAUS augmin-like complex, subunit 4	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241017	MGI			
1313229	Haus4	HAUS augmin-like complex, subunit 4	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1313229	Haus4	HAUS augmin-like complex, subunit 4	gene	MP:0004964	absent inner cell mass		IEA		N	RGD:5509061	20240919	MGI			
1313229	Haus4	HAUS augmin-like complex, subunit 4	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1313229	Haus4	HAUS augmin-like complex, subunit 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313229	Haus4	HAUS augmin-like complex, subunit 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1313234	Rasip1	Ras interacting protein 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313234	Rasip1	Ras interacting protein 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313234	Rasip1	Ras interacting protein 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313234	Rasip1	Ras interacting protein 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313234	Rasip1	Ras interacting protein 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0003542	abnormal vascular endothelial cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0003543	abnormal vascular endothelial cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313234	Rasip1	Ras interacting protein 1	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313234	Rasip1	Ras interacting protein 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313234	Rasip1	Ras interacting protein 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313234	Rasip1	Ras interacting protein 1	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313234	Rasip1	Ras interacting protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21396893
1313234	Rasip1	Ras interacting protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23886837
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032820
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032820
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032820
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032820
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032820
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032820
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1313239	Eif4g2	eukaryotic translation initiation factor 4, gamma 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20220519	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20201231	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680960
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20201231	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680960
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:20680960
1313246	Arid3a	AT-rich interaction domain 3A	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:21199920
1313248	Krt32	keratin 32	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20241121	MGI			
1313248	Krt32	keratin 32	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1313248	Krt32	keratin 32	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20230601	MGI			
1313248	Krt32	keratin 32	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1313248	Krt32	keratin 32	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20201231	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20181227	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1313250	Abce1	ATP-binding cassette, sub-family E member 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313251	Cdkn2aip	CDKN2A interacting protein	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1313251	Cdkn2aip	CDKN2A interacting protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1313251	Cdkn2aip	CDKN2A interacting protein	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1313251	Cdkn2aip	CDKN2A interacting protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20241121	MGI			
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20241121	MGI			
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20241121	MGI			
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20241121	MGI			
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17337443
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485511
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470642
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485511
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470642
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470642
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485511
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550345
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470642
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485511
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470642
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008592	decreased circulating interleukin-1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470642
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485511
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470642
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485511
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17337443
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470642
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470642
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485511
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923871
1313253	Irak4	interleukin-1 receptor-associated kinase 4	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20230608	MGI			PMID:17337443
1313255	Etnk2	ethanolamine kinase 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16861741
1313255	Etnk2	ethanolamine kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18755794
1313255	Etnk2	ethanolamine kinase 2	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16861741
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0001765	abnormal ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313259	Epb42	erythrocyte membrane protein band 4.2	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359562
1313262	Zdhhc1	zinc finger, DHHC domain containing 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20201015	MGI			PMID:25299331
1313262	Zdhhc1	zinc finger, DHHC domain containing 1	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20201015	MGI			PMID:25299331
1313262	Zdhhc1	zinc finger, DHHC domain containing 1	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20201015	MGI			PMID:25299331
1313262	Zdhhc1	zinc finger, DHHC domain containing 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20201015	MGI			PMID:25299331
1313262	Zdhhc1	zinc finger, DHHC domain containing 1	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20201015	MGI			PMID:25299331
1313262	Zdhhc1	zinc finger, DHHC domain containing 1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20201015	MGI			PMID:25299331
1313262	Zdhhc1	zinc finger, DHHC domain containing 1	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20201015	MGI			PMID:25299331
1313263	Xpnpep3	X-prolyl aminopeptidase 3, mitochondrial	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1313265	Neto2	neuropilin (NRP) and tolloid (TLL)-like 2	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20200514	MGI			
1313265	Neto2	neuropilin (NRP) and tolloid (TLL)-like 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1313265	Neto2	neuropilin (NRP) and tolloid (TLL)-like 2	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21734292
1313265	Neto2	neuropilin (NRP) and tolloid (TLL)-like 2	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1313265	Neto2	neuropilin (NRP) and tolloid (TLL)-like 2	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210520	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001127	small ovary		IEA		N	RGD:5509061	20210520	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210128	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200514	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0004857	abnormal heart weight		IEA		N	RGD:5509061	20260402	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199137
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20201022	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20200514	MGI			
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20210513	MGI			PMID:31924127
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:15107851
1313269	Cnot7	CCR4-NOT transcription complex, subunit 7	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1313272	Rnf115	ring finger protein 115	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1313272	Rnf115	ring finger protein 115	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1313272	Rnf115	ring finger protein 115	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20210429	MGI			PMID:33139700
1313272	Rnf115	ring finger protein 115	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1313272	Rnf115	ring finger protein 115	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1313272	Rnf115	ring finger protein 115	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20210429	MGI			PMID:33139700
1313272	Rnf115	ring finger protein 115	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20210429	MGI			PMID:33139700
1313272	Rnf115	ring finger protein 115	gene	MP:0009790	decreased susceptibility to viral infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210429	MGI			PMID:33139700
1313272	Rnf115	ring finger protein 115	gene	MP:0009791	increased susceptibility to viral infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210429	MGI			PMID:33139700
1313274	Btd	biotinidase	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0000756	forelimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313274	Btd	biotinidase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051254
1313276	Foxb2	forkhead box B2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1313276	Foxb2	forkhead box B2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1313279	Rcl1	RNA terminal phosphate cyclase-like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1313281	Mars1	methionine-tRNA synthetase 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1313281	Mars1	methionine-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1313283	Map4k4	mitogen-activated protein kinase kinase kinase kinase 4	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290295
1313283	Map4k4	mitogen-activated protein kinase kinase kinase kinase 4	gene	MP:0003445	sirenomelia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290295
1313283	Map4k4	mitogen-activated protein kinase kinase kinase kinase 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290295
1313283	Map4k4	mitogen-activated protein kinase kinase kinase kinase 4	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290295
1313283	Map4k4	mitogen-activated protein kinase kinase kinase kinase 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290295
1313283	Map4k4	mitogen-activated protein kinase kinase kinase kinase 4	gene	MP:0012739	abnormal anterior primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290295
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201231	MGI			
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20200514	MGI			
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0002544	brachydactyly		IEA		N	RGD:5509061	20200514	MGI			
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890158
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0004391	abnormal respiratory conducting tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200514	MGI			
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0010079	increased osteochondroma incidence		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20200514	MGI			
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0014277	alobar holoprosencephaly		IAGP		N	RGD:5509061	20230810	MGI			PMID:17156747
1313287	Spry4	sprouty RTK signaling antagonist 4	gene	MP:0031283	increased enchondroma incidence		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1313289	Plxna2	plexin A2	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327254
1313289	Plxna2	plexin A2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327254
1313289	Plxna2	plexin A2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327254
1313289	Plxna2	plexin A2	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1313289	Plxna2	plexin A2	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296555
1313289	Plxna2	plexin A2	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20484647
1313289	Plxna2	plexin A2	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327254
1313289	Plxna2	plexin A2	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24179230
1313289	Plxna2	plexin A2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24179230
1313289	Plxna2	plexin A2	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24179230
1313289	Plxna2	plexin A2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1313289	Plxna2	plexin A2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24179230
1313289	Plxna2	plexin A2	gene	MP:0014553	decreased neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:18327254
1313289	Plxna2	plexin A2	gene	MP:0014744	abnormal hippocampal mossy fiber suprapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:20484647
1313289	Plxna2	plexin A2	gene	MP:0014744	abnormal hippocampal mossy fiber suprapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:21270798
1313289	Plxna2	plexin A2	gene	MP:0014746	abnormal hippocampal mossy fiber innervation pattern		IAGP		N	RGD:5509061	20250911	MGI			PMID:17296555
1313289	Plxna2	plexin A2	gene	MP:0014746	abnormal hippocampal mossy fiber innervation pattern		IAGP		N	RGD:5509061	20250911	MGI			PMID:20484647
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210805	MGI			
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210805	MGI			
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20210805	MGI			
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210805	MGI			
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210805	MGI			
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20221215	MGI			
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20210805	MGI			
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20210819	MGI			PMID:29535165
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20210819	MGI			PMID:29535165
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20210819	MGI			PMID:29535165
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210805	MGI			
1313293	Txndc5	thioredoxin domain containing 5	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1313294	D5Ertd579e	DNA segment, Chr 5, ERATO Doi 579, expressed	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1313294	D5Ertd579e	DNA segment, Chr 5, ERATO Doi 579, expressed	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1313294	D5Ertd579e	DNA segment, Chr 5, ERATO Doi 579, expressed	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1313294	D5Ertd579e	DNA segment, Chr 5, ERATO Doi 579, expressed	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1313294	D5Ertd579e	DNA segment, Chr 5, ERATO Doi 579, expressed	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403930
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429434
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403930
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429434
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403930
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429434
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403930
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403930
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429434
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403930
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429434
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403930
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429434
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429434
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403930
1313296	Alox12b	arachidonate 12-lipoxygenase, 12R type	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17429434
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:18075202
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16469738
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964294
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16469738
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964294
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18075202
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456791
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0003968	abnormal growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964294
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964294
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18075202
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18075202
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964294
1313298	Tpst2	protein-tyrosine sulfotransferase 2	gene	MP:0008366	enlarged adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964294
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832751
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832751
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832751
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832751
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832751
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20362536
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936560
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936560
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002035	increased leiomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936560
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832751
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477326
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477327
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857802
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857803
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477326
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477327
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003010	decreased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003010	decreased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936560
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724834
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0008136	enlarged Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832751
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20260813	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0009591	increased liver adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477326
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0010318	increased salivary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22624716
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0010343	increased lipoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857803
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729946
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15607981
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20671749
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285512
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936560
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477326
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477327
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509446
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832750
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832751
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17526734
1313300	Mdm2	MDM2 proto-oncogene	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:23770245
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20160602	MGI			PMID:27163549
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20160602	MGI			PMID:27163549
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180412	MGI			PMID:23583447
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20180412	MGI			PMID:23583447
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160602	MGI			PMID:27163549
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20160602	MGI			PMID:27163549
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20160602	MGI			PMID:27163549
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160602	MGI			PMID:27163549
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160602	MGI			PMID:27163549
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20160602	MGI			PMID:27163549
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20160602	MGI			PMID:27163549
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20180412	MGI			PMID:23583447
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0008409	increased cellular sensitivity to hydroxyurea induced cell death		IAGP		N	RGD:5509061	20180412	MGI			PMID:23583447
1313305	Ciz1	CDKN1A interacting zinc finger protein 1	gene	MP:0012563	increased tumor incidence following infection		IAGP		N	RGD:5509061	20180412	MGI			PMID:23583447
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0010770	preweaning lethality		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313308	Hic2	hypermethylated in cancer 2	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1313310	Dap3	death associated protein 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135360
1313310	Dap3	death associated protein 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135360
1313310	Dap3	death associated protein 3	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135360
1313310	Dap3	death associated protein 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1313310	Dap3	death associated protein 3	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135360
1313310	Dap3	death associated protein 3	gene	MP:0004258	abnormal placenta size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135360
1313310	Dap3	death associated protein 3	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135360
1313310	Dap3	death associated protein 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135360
1313310	Dap3	death associated protein 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313310	Dap3	death associated protein 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313310	Dap3	death associated protein 3	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17135360
1313317	Emilin2	elastin microfibril interfacer 2	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1313317	Emilin2	elastin microfibril interfacer 2	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20160414	MGI			PMID:25658937
1313317	Emilin2	elastin microfibril interfacer 2	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20160414	MGI			PMID:25658937
1313317	Emilin2	elastin microfibril interfacer 2	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160414	MGI			PMID:25658937
1313317	Emilin2	elastin microfibril interfacer 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20240404	MGI			PMID:38370417
1313318	Iglon5	IgLON family member 5	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20240404	MGI			PMID:38370417
1313318	Iglon5	IgLON family member 5	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20240404	MGI			PMID:38370417
1313318	Iglon5	IgLON family member 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20240404	MGI			PMID:38370417
1313318	Iglon5	IgLON family member 5	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1313318	Iglon5	IgLON family member 5	gene	MP:0009710	anhedonia		IAGP		N	RGD:5509061	20240404	MGI			PMID:38370417
1313318	Iglon5	IgLON family member 5	gene	MP:0020379	abnormal sucrose solution preference		IAGP		N	RGD:5509061	20240404	MGI			PMID:38370417
1313321	Farp1	FERM, ARH/RhoGEF and pleckstrin domain protein 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210128	MGI			
1313321	Farp1	FERM, ARH/RhoGEF and pleckstrin domain protein 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1313321	Farp1	FERM, ARH/RhoGEF and pleckstrin domain protein 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1313321	Farp1	FERM, ARH/RhoGEF and pleckstrin domain protein 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1313323	Cep152	centrosomal protein 152	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24706806
1313323	Cep152	centrosomal protein 152	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20150129	MGI			PMID:24706806
1313323	Cep152	centrosomal protein 152	gene	MP:0013214	decreased embryonic neuroepithelium primary cilium number		IAGP		N	RGD:5509061	20150129	MGI			PMID:24706806
1313323	Cep152	centrosomal protein 152	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:24706806
1313325	2510039O18Rik	RIKEN cDNA 2510039O18 gene	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1313327	Lyar	Ly1 antibody reactive clone	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
1313327	Lyar	Ly1 antibody reactive clone	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
1313327	Lyar	Ly1 antibody reactive clone	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
1313327	Lyar	Ly1 antibody reactive clone	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
1313327	Lyar	Ly1 antibody reactive clone	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
1313327	Lyar	Ly1 antibody reactive clone	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210520	MGI			
1313327	Lyar	Ly1 antibody reactive clone	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1313327	Lyar	Ly1 antibody reactive clone	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
1313327	Lyar	Ly1 antibody reactive clone	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20180809	MGI			PMID:22815056
1313329	Matn2	matrilin 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1313329	Matn2	matrilin 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296947
1313329	Matn2	matrilin 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1313329	Matn2	matrilin 2	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1313329	Matn2	matrilin 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1313329	Matn2	matrilin 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1313329	Matn2	matrilin 2	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1313329	Matn2	matrilin 2	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20190502	MGI			
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0006325	impaired hearing		IEA		N	RGD:5509061	20111116	MGI			
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0009511	distended stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0009644	uremia		IEA		N	RGD:5509061	20111116	MGI			
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011418	leukocyturia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011425	abnormal kidney interstitium morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011483	renal glomerular synechia		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20151126	MGI			PMID:24522496
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011871	podocyte hypertrophy		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20210211	MGI			PMID:31892712
1313333	Col4a4	collagen, type IV, alpha 4	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196518
1313335	Unc45a	unc-45 myosin chaperone A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1313335	Unc45a	unc-45 myosin chaperone A	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20260402	MGI			
1313335	Unc45a	unc-45 myosin chaperone A	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20260402	MGI			
1313335	Unc45a	unc-45 myosin chaperone A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313337	B4galt2	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265195
1313337	B4galt2	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265195
1313337	B4galt2	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265195
1313337	B4galt2	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265195
1313337	B4galt2	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265195
1313337	B4galt2	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265195
1313337	B4galt2	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	gene	MP:0006097	abnormal cerebellar lobule formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265195
1313337	B4galt2	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265195
1313337	B4galt2	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265195
1313340	Acap1	ArfGAP with coiled-coil, ankyrin repeat and PH domains 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1313345	Mapkap1	mitogen-activated protein kinase associated protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1313345	Mapkap1	mitogen-activated protein kinase associated protein 1	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20190502	MGI			
1313345	Mapkap1	mitogen-activated protein kinase associated protein 1	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962653
1313345	Mapkap1	mitogen-activated protein kinase associated protein 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962653
1313345	Mapkap1	mitogen-activated protein kinase associated protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313345	Mapkap1	mitogen-activated protein kinase associated protein 1	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20210520	MGI			
1313345	Mapkap1	mitogen-activated protein kinase associated protein 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1313345	Mapkap1	mitogen-activated protein kinase associated protein 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1313345	Mapkap1	mitogen-activated protein kinase associated protein 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16962653
1313347	Tes	testin LIM domain protein	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16033868
1313347	Tes	testin LIM domain protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937400
1313347	Tes	testin LIM domain protein	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16033868
1313347	Tes	testin LIM domain protein	gene	MP:0013575	abnormal forestomach-glandular stomach junction morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:16033868
1313347	Tes	testin LIM domain protein	gene	MP:0013576	small forestomach		IAGP		N	RGD:5509061	20150305	MGI			PMID:16033868
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889634
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889634
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889634
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807321
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889634
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0010714	iris coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889634
1313349	Hs2st1	heparan sulfate 2-O-sulfotransferase 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637690
1313351	Gtpbp3	GTP binding protein 3	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313351	Gtpbp3	GTP binding protein 3	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313351	Gtpbp3	GTP binding protein 3	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313351	Gtpbp3	GTP binding protein 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313353	Klhl40	kelch-like 40	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160526	MGI			PMID:25940086
1313353	Klhl40	kelch-like 40	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:25940086
1313353	Klhl40	kelch-like 40	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20160526	MGI			PMID:25940086
1313353	Klhl40	kelch-like 40	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20160526	MGI			PMID:25940086
1313353	Klhl40	kelch-like 40	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160526	MGI			PMID:25940086
1313353	Klhl40	kelch-like 40	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160616	MGI			PMID:24960163
1313353	Klhl40	kelch-like 40	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313353	Klhl40	kelch-like 40	gene	MP:0020240	increased skeletal muscle cell apoptosis		IAGP		N	RGD:5509061	20160526	MGI			PMID:25940086
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000615	abnormal palatine gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000615	abnormal palatine gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000616	decreased ductal branching in the palatine gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000617	increased salivary gland mucosal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000618	small salivary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000619	salivary gland epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000620	narrow salivary ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000660	prostate gland lateral lobe hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000661	small prostate gland ventral lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000664	small prostate gland anterior lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000664	small prostate gland anterior lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000665	decreased ductal branching in the coagulating gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000665	decreased ductal branching in the coagulating gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000666	decreased prostate gland duct number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000666	decreased prostate gland duct number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000666	decreased prostate gland duct number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0000671	bulbourethral gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494112
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002344
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001169	abnormal bulbourethral gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22836754
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0002009	preneoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0002009	preneoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11839815
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0002009	preneoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111307
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22836754
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0003791	abnormal minor salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0005305	prostate gland anterior lobe hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0005305	prostate gland anterior lobe hyperplasia		IAGP		N	RGD:5509061	20220303	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11839815
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854455
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111307
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18245377
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741607
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22836754
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741607
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22836754
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009517	abnormal salivary gland duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009734	abnormal prostate gland duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494112
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009736	abnormal prostate gland branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009736	abnormal prostate gland branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494112
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0009736	abnormal prostate gland branching morphogenesis		IAGP		N	RGD:5509061	20220303	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854455
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22836754
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12204261
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0011781	abnormal bulbourethral gland physiology		IAGP		N	RGD:5509061	20150326	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0013736	abnormal bulbourethral gland development		IAGP		N	RGD:5509061	20150416	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0013736	abnormal bulbourethral gland development		IAGP		N	RGD:5509061	20150416	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0013737	small bulbourethral gland		IAGP		N	RGD:5509061	20150416	MGI			PMID:10906459
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0031369	prostate gland dorsolateral lobe hyperplasia		IAGP		N	RGD:5509061	20220303	MGI			PMID:10215624
1313355	Nkx3-1	NK3 homeobox 1	gene	MP:0031369	prostate gland dorsolateral lobe hyperplasia		IAGP		N	RGD:5509061	20220303	MGI			PMID:10906459
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973269
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973269
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001687	thin endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973269
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20221006	MGI			PMID:36046192
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19548312
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22121118
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19619492
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003250	absent gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:19619492
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003251	gallbladder inflammation		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003279	aneurysm		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003655	absent pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:19619492
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0004044	aortic dissection		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973269
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20221006	MGI			PMID:36046192
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005084	abnormal gallbladder morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005084	abnormal gallbladder morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005085	abnormal gallbladder physiology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973269
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005385	cardiovascular system phenotype		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005414	extrahepatic cholestasis		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0005675	small gallbladder		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0008786	abnormal hindgut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973269
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0008987	abnormal liver lobule morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009489	abnormal blood vessel endothelium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009492	abnormal gallbladder epithelium morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009492	abnormal gallbladder epithelium morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009493	abnormal cystic duct morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009495	abnormal common bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19619492
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009498	abnormal extrahepatic bile duct morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009705	abnormal midgut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973269
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0009870	abnormal abdominal aorta morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0010468	abnormal thoracic aorta morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180215	MGI			PMID:23293295
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973269
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17655922
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0012084	truncated foregut		IAGP		N	RGD:5509061	20221006	MGI			PMID:36046192
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0012201	decreased endothelial cell proliferation		IAGP		N	RGD:5509061	20160929	MGI			PMID:25596186
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0014010	abnormal peroxisome morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0014451	decreased circulating enzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:25141153
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0020134	abnormal gallbladder size		IAGP		N	RGD:5509061	20180215	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0031021	abnormal gallbladder smooth muscle morphology		IAGP		N	RGD:5509061	20200227	MGI			PMID:28432216
1313359	Sox17	SRY (sex determining region Y)-box 17	gene	MP:0031315	biliary atresia		IAGP		N	RGD:5509061	20211104	MGI			PMID:28432216
1313361	Ncbp2	nuclear cap binding protein subunit 2	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20181227	MGI			
1313361	Ncbp2	nuclear cap binding protein subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313361	Ncbp2	nuclear cap binding protein subunit 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313363	Eif6	eukaryotic translation initiation factor 6	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18784653
1313363	Eif6	eukaryotic translation initiation factor 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18784653
1313363	Eif6	eukaryotic translation initiation factor 6	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18784653
1313363	Eif6	eukaryotic translation initiation factor 6	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18784653
1313363	Eif6	eukaryotic translation initiation factor 6	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18784653
1313363	Eif6	eukaryotic translation initiation factor 6	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18784653
1313363	Eif6	eukaryotic translation initiation factor 6	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18784653
1313363	Eif6	eukaryotic translation initiation factor 6	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18784653
1313363	Eif6	eukaryotic translation initiation factor 6	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18784653
1313369	Best2	bestrophin 2	gene	MP:0005257	abnormal intraocular pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385076
1313369	Best2	bestrophin 2	gene	MP:0005260	ocular hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385076
1313369	Best2	bestrophin 2	gene	MP:0005544	cornea deposits		IEA		N	RGD:5509061	20201231	MGI			
1313369	Best2	bestrophin 2	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385076
1313369	Best2	bestrophin 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313371	Mtmr6	myotubularin related protein 6	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1313371	Mtmr6	myotubularin related protein 6	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1313371	Mtmr6	myotubularin related protein 6	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1313371	Mtmr6	myotubularin related protein 6	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1313371	Mtmr6	myotubularin related protein 6	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1313371	Mtmr6	myotubularin related protein 6	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20260402	MGI			
1313371	Mtmr6	myotubularin related protein 6	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20260402	MGI			
1313371	Mtmr6	myotubularin related protein 6	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20260402	MGI			
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20231207	MGI			
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950870
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950870
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20231207	MGI			
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950870
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20231207	MGI			
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950870
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950870
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950870
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950870
1313373	Clcn6	chloride channel, voltage-sensitive 6	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20240523	MGI			
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000397	abnormal guard hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002683	delayed fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003315	abnormal perineum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21875955
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15353549
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20171102	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810584
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15353549
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15353549
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20160915	MGI			PMID:25252918
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0005299	abnormal eye posterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231717
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0006310	increased retinoblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17235288
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0006310	increased retinoblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363591
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0006399	abnormal long bone epiphyseal ossification zone morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0008161	increased diameter of radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0008163	increased diameter of ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0008218	delayed emergence of vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702649
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:25252918
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16271529
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150212	MGI			PMID:24710275
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9819431
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:20585628
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:8682293
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:8682294
1313375	Rbl1	RB transcriptional corepressor like 1	gene	MP:0030079	small incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:12702649
1313377	Relt	RELT tumor necrosis factor receptor	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20200402	MGI			PMID:30138536
1313377	Relt	RELT tumor necrosis factor receptor	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:30506946
1313377	Relt	RELT tumor necrosis factor receptor	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200402	MGI			PMID:30138536
1313377	Relt	RELT tumor necrosis factor receptor	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:30138536
1313377	Relt	RELT tumor necrosis factor receptor	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20191128	MGI			PMID:30506946
1313379	Ube2c	ubiquitin-conjugating enzyme E2C	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1313379	Ube2c	ubiquitin-conjugating enzyme E2C	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1313379	Ube2c	ubiquitin-conjugating enzyme E2C	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1313379	Ube2c	ubiquitin-conjugating enzyme E2C	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1313379	Ube2c	ubiquitin-conjugating enzyme E2C	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1313379	Ube2c	ubiquitin-conjugating enzyme E2C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313379	Ube2c	ubiquitin-conjugating enzyme E2C	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9307064
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0014350	disorganized spleen B cell follicle		IAGP		N	RGD:5509061	20240104	MGI			PMID:17142749
1313381	Arhgdib	Rho, GDP dissociation inhibitor beta	gene	MP:0014471	enhanced B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:17142749
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651524
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22539351
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22539351
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651524
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651524
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224198
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20210128	MGI			
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651524
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651524
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224198
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651524
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224198
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20240801	MGI			PMID:19224198
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22539351
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651524
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0012415	decreased sarcoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:23412344
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0030974	enhanced gluconeogenesis		IAGP		N	RGD:5509061	20200102	MGI			PMID:19224198
1313383	Cpt1c	carnitine palmitoyltransferase 1c	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:19224198
1313385	Asb16	ankyrin repeat and SOCS box-containing 16	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20200514	MGI			
1313385	Asb16	ankyrin repeat and SOCS box-containing 16	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20200514	MGI			
1313385	Asb16	ankyrin repeat and SOCS box-containing 16	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20200514	MGI			
1313385	Asb16	ankyrin repeat and SOCS box-containing 16	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20200514	MGI			
1313393	Plk4	polo like kinase 4	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791561
1313393	Plk4	polo like kinase 4	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301255
1313393	Plk4	polo like kinase 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301255
1313393	Plk4	polo like kinase 4	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301255
1313393	Plk4	polo like kinase 4	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791561
1313393	Plk4	polo like kinase 4	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301255
1313393	Plk4	polo like kinase 4	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301255
1313393	Plk4	polo like kinase 4	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791561
1313393	Plk4	polo like kinase 4	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791561
1313393	Plk4	polo like kinase 4	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301255
1313393	Plk4	polo like kinase 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791561
1313393	Plk4	polo like kinase 4	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301255
1313397	Cpne6	copine VI	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20190307	MGI			PMID:27194588
1313397	Cpne6	copine VI	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20190307	MGI			PMID:27194588
1313397	Cpne6	copine VI	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20190307	MGI			PMID:27194588
1313397	Cpne6	copine VI	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20190307	MGI			PMID:27194588
1313397	Cpne6	copine VI	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:27194588
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15615595
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15615595
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15615595
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15615595
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15615595
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20181227	MGI			
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15615595
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15615595
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20181227	MGI			
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15615595
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0010503	myocardial trabeculae hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15615595
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345036
1313401	Jmjd6	jumonji domain containing 6	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:15345036
1313403	Rsu1	Ras suppressor protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220811	MGI			
1313403	Rsu1	Ras suppressor protein 1	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20220811	MGI			
1313403	Rsu1	Ras suppressor protein 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210520	MGI			
1313403	Rsu1	Ras suppressor protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313405	Rbsn	rabenosyn, RAB effector	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0011208	small proamniotic cavity		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1313407	Taf13	TATA-box binding protein associated factor 13	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:11961557
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7479980
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:26114879
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170223	MGI			PMID:26114879
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20220407	MGI			PMID:34625556
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426143
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16455962
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960379
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548588
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960379
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135325
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7479980
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20201224	MGI			PMID:30591559
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123129
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20170223	MGI			PMID:26114879
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200423	MGI			PMID:16985170
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960379
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21458307
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20170223	MGI			PMID:26114879
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17190817
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20170223	MGI			PMID:26114879
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20200423	MGI			PMID:16985170
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20171026	MGI			PMID:22802351
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209048
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548588
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004795	decreased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20170223	MGI			PMID:26114879
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11961557
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148148
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370359
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17190817
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548588
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20220616	MGI			PMID:34343497
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17051153
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7479980
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20200827	MGI			PMID:26867177
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548588
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200827	MGI			PMID:26867177
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200827	MGI			PMID:26867177
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008248	abnormal mononuclear phagocyte morphology		IAGP		N	RGD:5509061	20200827	MGI			PMID:26867177
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16455962
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16455962
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16455962
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20170223	MGI			PMID:26114879
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209048
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389237
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389237
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20170223	MGI			PMID:26114879
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209048
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20200827	MGI			PMID:26867177
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0009851	abnormal Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0010750	increased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370359
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0010855	pulmonary hyperemia		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20171026	MGI			PMID:22802351
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0013023	decreased Ly6C high monocyte number		IAGP		N	RGD:5509061	20200827	MGI			PMID:26867177
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:17066036
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:26114879
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:10209048
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11390995
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23449591
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020928	increased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16123129
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020931	increased susceptibility to Adenoviridae infection		IEA		N	RGD:5509061	20200430	MGI			
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16625202
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200514	MGI			PMID:7479980
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020940	increased susceptibility to Togaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11390995
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020940	increased susceptibility to Togaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:7479980
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:10400797
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:10400797
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16985170
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020950	decreased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200827	MGI			PMID:26867177
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020952	increased susceptibility to Paramyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17135325
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0020952	increased susceptibility to Paramyxoviridae infection		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:9687534
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0031040	increased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:7479980
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0031042	increased susceptibility to Togaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:7479980
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0031045	decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:10400797
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200827	MGI			PMID:26867177
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200827	MGI			PMID:16985170
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200827	MGI			PMID:26867177
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0031050	increased susceptibility to Paramyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313409	Ifnar1	interferon (alpha and beta) receptor 1	gene	MP:0031110	meningitis		IAGP		N	RGD:5509061	20210211	MGI			PMID:9696838
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20230119	MGI			
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20210128	MGI			
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230119	MGI			
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0009127	increased brown fat cell number		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0020868	decreased lipogenesis		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313410	Ccdc92	coiled-coil domain containing 92	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20230202	MGI			PMID:36594018
1313414	Commd8	COMM domain containing 8	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0008191	abnormal follicular B cell physiology		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313414	Commd8	COMM domain containing 8	gene	MP:0013940	abnormal plasmablast number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210819
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210819
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210819
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210819
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210819
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313417	Lect2	leukocyte cell-derived chemotaxin 2	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22251704
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0012338	decreased bile salt level		IAGP		N	RGD:5509061	20171116	MGI			PMID:26586440
1313420	Smarcd1	SWI/SNF related BAF chromatin remodeling complex subunit D1	gene	MP:0014480	increased feces cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:26586440
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7864091
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:4123573
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6527158
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20220519	MGI			
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1372391
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1372391
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11136708
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:4123573
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7864091
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:1372391
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20220519	MGI			
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:4123573
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:6527158
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7864091
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:4123573
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:4123573
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:1372391
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7864091
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4123573
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1372391
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0004243	abnormal motor nerve collateral sprouting		IAGP		N	RGD:5509061	20141003	MGI			PMID:1372391
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0004684	intervertebral disk degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:6527158
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20220519	MGI			
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0006392	abnormal nucleus pulposus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6527158
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0006393	absent nucleus pulposus		IAGP		N	RGD:5509061	20141003	MGI			PMID:6527158
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0009424	decreased extensor digitorum longus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7864091
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0009426	decreased soleus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7864091
1313422	Ky	kyphoscoliosis peptidase	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1313429	Cdc34	cell division cycle 34	gene	MP:0000579	abnormal nail morphology		IEA		N	RGD:5509061	20181227	MGI			
1313429	Cdc34	cell division cycle 34	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1313429	Cdc34	cell division cycle 34	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313429	Cdc34	cell division cycle 34	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1313431	Mroh2b	maestro heat-like repeat family member 2B	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20250605	MGI			PMID:27105888
1313431	Mroh2b	maestro heat-like repeat family member 2B	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:27105888
1313431	Mroh2b	maestro heat-like repeat family member 2B	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20250605	MGI			PMID:27105888
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20181227	MGI			
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048919
1313433	Uchl5	ubiquitin carboxyl-terminal esterase L5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313438	Polr2e	polymerase (RNA) II (DNA directed) polypeptide E	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20260402	MGI			
1313440	Rars2	arginyl-tRNA synthetase 2, mitochondrial	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1313440	Rars2	arginyl-tRNA synthetase 2, mitochondrial	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1313442	Trmo	tRNA methyltransferase O	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1313442	Trmo	tRNA methyltransferase O	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1313444	Rubcn	RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20180920	MGI			PMID:26098576
1313444	Rubcn	RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20180920	MGI			PMID:26098576
1313445	Efcab3	EF-hand calcium binding domain 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1313445	Efcab3	EF-hand calcium binding domain 3	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20200220	MGI			PMID:30275530
1313445	Efcab3	EF-hand calcium binding domain 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20200220	MGI			PMID:30275530
1313445	Efcab3	EF-hand calcium binding domain 3	gene	MP:0008914	enlarged cerebellum		IAGP		N	RGD:5509061	20200220	MGI			PMID:30275530
1313445	Efcab3	EF-hand calcium binding domain 3	gene	MP:0020563	increased pontine nuclei size		IAGP		N	RGD:5509061	20200220	MGI			PMID:30275530
1313450	Supt3	SPT3, SAGA and STAGA complex component	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313450	Supt3	SPT3, SAGA and STAGA complex component	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313450	Supt3	SPT3, SAGA and STAGA complex component	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313450	Supt3	SPT3, SAGA and STAGA complex component	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313450	Supt3	SPT3, SAGA and STAGA complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320163
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320163
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320163
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320163
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0003364	increased insulinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0003492	abnormal involuntary movement		IEA		N	RGD:5509061	20111116	MGI			
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320163
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320163
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0011087	neonatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313453	Kdm5a	lysine demethylase 5A	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788502
1313459	Siglecf	sialic acid binding Ig-like lectin F	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17272508
1313459	Siglecf	sialic acid binding Ig-like lectin F	gene	MP:0002443	abnormal eosinophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17272508
1313459	Siglecf	sialic acid binding Ig-like lectin F	gene	MP:0002465	abnormal eosinophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17272508
1313459	Siglecf	sialic acid binding Ig-like lectin F	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17272508
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38694206
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20210826	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20181227	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20240523	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38694206
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0002959	increased urine microalbumin level		IEA		N	RGD:5509061	20211021	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38694206
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38694206
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0012338	decreased bile salt level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38694206
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0013275	abnormal xenobiotic metabolism		IAGP		N	RGD:5509061	20240530	MGI			PMID:38694206
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1313460	Gramd1c	GRAM domain containing 1C	gene	MP:0014161	increased circulating cortisol level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38694206
1313467	Tex14	testis expressed gene 14 intercellular bridge forming factor	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16549803
1313467	Tex14	testis expressed gene 14 intercellular bridge forming factor	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16549803
1313467	Tex14	testis expressed gene 14 intercellular bridge forming factor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16549803
1313467	Tex14	testis expressed gene 14 intercellular bridge forming factor	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16549803
1313467	Tex14	testis expressed gene 14 intercellular bridge forming factor	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16549803
1313467	Tex14	testis expressed gene 14 intercellular bridge forming factor	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16549803
1313467	Tex14	testis expressed gene 14 intercellular bridge forming factor	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16549803
1313467	Tex14	testis expressed gene 14 intercellular bridge forming factor	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16549803
1313469	Cdh20	cadherin 20	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20240523	MGI			
1313469	Cdh20	cadherin 20	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1313471	Ubox5	U box domain containing 5	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20220519	MGI			
1313471	Ubox5	U box domain containing 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20200310	MGI			
1313471	Ubox5	U box domain containing 5	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20191024	MGI			PMID:30220461
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20210520	MGI			
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20210520	MGI			
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30220461
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20191024	MGI			PMID:30220461
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20191024	MGI			PMID:30220461
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0008294	abnormal adrenal gland zona fasciculata morphology		IAGP		N	RGD:5509061	20191024	MGI			PMID:30220461
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313474	Gramd1b	GRAM domain containing 1B	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20210520	MGI			
1313476	Prrg2	proline-rich Gla (G-carboxyglutamic acid) polypeptide 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1313476	Prrg2	proline-rich Gla (G-carboxyglutamic acid) polypeptide 2	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1313478	Ltf	lactotransferrin	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20160915	MGI			PMID:25057912
1313478	Ltf	lactotransferrin	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24823394
1313478	Ltf	lactotransferrin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25057912
1313478	Ltf	lactotransferrin	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20160915	MGI			PMID:25057912
1313478	Ltf	lactotransferrin	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482971
1313478	Ltf	lactotransferrin	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20160915	MGI			PMID:25057912
1313478	Ltf	lactotransferrin	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482971
1313478	Ltf	lactotransferrin	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482971
1313478	Ltf	lactotransferrin	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482971
1313478	Ltf	lactotransferrin	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0009649	delayed embryo implantation		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0009662	abnormal uterine receptivity		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313478	Ltf	lactotransferrin	gene	MP:0009666	abnormal embryo attachment		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:24297939
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0008030	abnormal Cajal-Retzius cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24297939
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0012129	failure of blastocyst formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24297939
1313481	Pomt2	protein-O-mannosyltransferase 2	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:24297939
1313483	Trim11	tripartite motif-containing 11	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20221027	MGI			PMID:36192394
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0000861	disorganized barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092954
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346763
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092954
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346763
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346763
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0002735	abnormal chemical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346763
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24327562
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346763
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0004562	abnormal inner hair cell synaptic ribbon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24327562
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346763
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0006075	abnormal retina cone bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092954
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346763
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092954
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092954
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346763
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0009681	abnormal pyramidal decussation morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0009682	abnormal anterior corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18957218
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0009682	abnormal anterior corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1313487	Bhlhe22	basic helix-loop-helix family, member e22	gene	MP:0014747	abnormal motor neuron axon guidance		IAGP		N	RGD:5509061	20250904	MGI			PMID:22284184
1313489	Cct8	chaperonin containing TCP1 subunit 8	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20240926	MGI			
1313489	Cct8	chaperonin containing TCP1 subunit 8	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20240926	MGI			
1313489	Cct8	chaperonin containing TCP1 subunit 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1313489	Cct8	chaperonin containing TCP1 subunit 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230601	MGI			
1313489	Cct8	chaperonin containing TCP1 subunit 8	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201231	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20190502	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20190502	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20190502	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20190502	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20190502	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0012246	abnormal hepatic cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20161201	MGI			PMID:20498273
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313492	Psmg1	proteasome (prosome, macropain) assembly chaperone 1	gene	MP:0013551	decreased cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20161201	MGI			PMID:20498273
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000413	polyphalangy		IAGP		N	RGD:5509061	20200310	MGI			PMID:6067640
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000464	increased presacral vertebrae number		IEA		N	RGD:5509061	20111116	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000482	long fibula		IEA		N	RGD:5509061	20111116	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:6067640
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:6067640
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000568	ectopic digits		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000568	ectopic digits		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20231207	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:6067640
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23727884
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156142
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20231207	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20231207	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001922	reduced male fertility		IEA		N	RGD:5509061	20111116	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:5088020
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:6067640
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20111116	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:6067640
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002543	brachyphalangia		IEA		N	RGD:5509061	20111116	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20200310	MGI			PMID:6067640
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004049	increased acute promyelocytic leukemia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:11106752
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004372	bowed fibula		IEA		N	RGD:5509061	20111116	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004651	increased thoracic vertebrae number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004679	xiphoid process foramen		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004694	absent patella		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156142
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0005109	abnormal talus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0005109	abnormal talus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15156142
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:5088020
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18703361
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0008159	increased diameter of fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0008159	increased diameter of fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:20338044
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0008159	increased diameter of fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:6067640
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23727884
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23727884
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0008985	hemimelia		IEA		N	RGD:5509061	20111116	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23727884
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230119	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20200310	MGI			PMID:23727884
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0012284	increased sternebra number		IEA		N	RGD:5509061	20200310	MGI			
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0014281	hindlimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:10835630
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250220	MGI			PMID:15156143
1313496	Zbtb16	zinc finger and BTB domain containing 16	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158963
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158963
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158963
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19619499
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809801
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19619499
1313499	Ppm1d	protein phosphatase 1D magnesium-dependent, delta isoform	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11809801
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000537	abnormal urethra morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000632	abnormal pineal gland morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000653	abnormal sex gland morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251665
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251665
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251665
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0003742	narrow head		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251665
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251665
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0009688	abnormal spinal cord central canal morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251665
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0012303	umbilical vein stenosis		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702401
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0012704	abnormal embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0012705	increased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20619750
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0013362	absent pineal gland		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0013842	ductus venosus stenosis		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0013849	absent abducens nerve		IAGP		N	RGD:5509061	20180809	MGI			PMID:27447114
1313501	Trp53bp2	transformation related protein 53 binding protein 2	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:20619750
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313503	Gpt2	glutamic pyruvate transaminase (alanine aminotransferase) 2	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20170216	MGI			PMID:27601654
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17115060
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414772
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414772
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17115060
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17115060
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17115060
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414772
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414772
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414772
1313505	Map4k1	mitogen-activated protein kinase kinase kinase kinase 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414772
1313508	Fbxo10	F-box protein 10	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210729	MGI			PMID:33914737
1313508	Fbxo10	F-box protein 10	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20201022	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20210128	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20181227	MGI			
1313508	Fbxo10	F-box protein 10	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20181227	MGI			
1313511	Prpf8	pre-mRNA processing factor 8	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811066
1313511	Prpf8	pre-mRNA processing factor 8	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1313511	Prpf8	pre-mRNA processing factor 8	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1313511	Prpf8	pre-mRNA processing factor 8	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811066
1313511	Prpf8	pre-mRNA processing factor 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20181227	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20181227	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313513	Alg8	ALG8 alpha-1,3-glucosyltransferase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1313518	Atf6	activating transcription factor 6	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765679
1313518	Atf6	activating transcription factor 6	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765679
1313518	Atf6	activating transcription factor 6	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20150212	MGI			PMID:24225943
1313518	Atf6	activating transcription factor 6	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:26029869
1313518	Atf6	activating transcription factor 6	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:26029869
1313518	Atf6	activating transcription factor 6	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:26029869
1313518	Atf6	activating transcription factor 6	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765679
1313518	Atf6	activating transcription factor 6	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20220310	MGI			PMID:26029869
1313518	Atf6	activating transcription factor 6	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765679
1313518	Atf6	activating transcription factor 6	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150212	MGI			PMID:24225943
1313518	Atf6	activating transcription factor 6	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765680
1313518	Atf6	activating transcription factor 6	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765679
1313518	Atf6	activating transcription factor 6	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765680
1313518	Atf6	activating transcription factor 6	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20220310	MGI			PMID:26029869
1313518	Atf6	activating transcription factor 6	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20220310	MGI			PMID:26029869
1313518	Atf6	activating transcription factor 6	gene	MP:0014121	increased pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20160324	MGI			PMID:24225943
1313518	Atf6	activating transcription factor 6	gene	MP:0020352	abnormal endoplasmic reticulum physiology		IAGP		N	RGD:5509061	20161013	MGI			PMID:17765679
1313518	Atf6	activating transcription factor 6	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:26029869
1313521	Spag7	sperm associated antigen 7	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20250508	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20260402	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20260402	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
1313521	Spag7	sperm associated antigen 7	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20181227	MGI			
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20210520	MGI			
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20250508	MGI			
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889154
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889154
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889154
1313523	L3mbtl3	L3MBTL3 histone methyl-lysine binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1313524	Thoc7	THO complex 7	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240919	MGI			
1313524	Thoc7	THO complex 7	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1313524	Thoc7	THO complex 7	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1313524	Thoc7	THO complex 7	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1313524	Thoc7	THO complex 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313524	Thoc7	THO complex 7	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20240523	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150924	MGI			PMID:25092767
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20240523	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20210617	MGI			PMID:33658388
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20210617	MGI			PMID:33658388
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20210617	MGI			PMID:33658388
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20240523	MGI			
1313526	Mki67	antigen identified by monoclonal antibody Ki 67	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20240523	MGI			
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20170525	MGI			
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0003631	nervous system phenotype		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313528	Elp6	elongator acetyltransferase complex subunit 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20260122	MGI			PMID:35698786
1313533	Sfr1	SWI5 dependent recombination repair 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20250508	MGI			
1313533	Sfr1	SWI5 dependent recombination repair 1	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20200402	MGI			
1313533	Sfr1	SWI5 dependent recombination repair 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20260402	MGI			
1313533	Sfr1	SWI5 dependent recombination repair 1	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20200402	MGI			
1313533	Sfr1	SWI5 dependent recombination repair 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1313533	Sfr1	SWI5 dependent recombination repair 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1313533	Sfr1	SWI5 dependent recombination repair 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1313533	Sfr1	SWI5 dependent recombination repair 1	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20260402	MGI			
1313533	Sfr1	SWI5 dependent recombination repair 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313535	Lrrn2	leucine rich repeat protein 2, neuronal	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20141003	MGI			
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785530
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628019
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785530
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628019
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785530
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785530
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264106
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515784
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515784
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628019
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628019
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10753224
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628019
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785530
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515784
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20211021	MGI			PMID:34489406
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264106
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785530
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785530
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785530
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628019
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0009797	abnormal mismatch repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264106
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0009797	abnormal mismatch repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628019
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785530
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628019
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0014765	enhanced mismatch repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:18264106
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0014766	impaired mismatch repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:20624957
1313537	Pms2	PMS1 homolog2, mismatch repair system component	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:17785530
1313539	Dpep3	dipeptidase 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210107	MGI			PMID:31212048
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11265752
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0009706	absent midgut		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463846
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313547	Runx1t1	RUNX1 translocation partner 1	gene	MP:0012423	decreased nervous system tumor incidence		IAGP		N	RGD:5509061	20260604	MGI			PMID:38992040
1313549	Rnf2	ring finger protein 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183370
1313549	Rnf2	ring finger protein 2	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183370
1313549	Rnf2	ring finger protein 2	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183370
1313549	Rnf2	ring finger protein 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313549	Rnf2	ring finger protein 2	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183370
1313549	Rnf2	ring finger protein 2	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183370
1313549	Rnf2	ring finger protein 2	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20260813	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19755104
1313549	Rnf2	ring finger protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1313549	Rnf2	ring finger protein 2	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039844
1313550	Gpbp1	GC-rich promoter binding protein 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1313550	Gpbp1	GC-rich promoter binding protein 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20181227	MGI			
1313550	Gpbp1	GC-rich promoter binding protein 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1313550	Gpbp1	GC-rich promoter binding protein 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20210128	MGI			
1313550	Gpbp1	GC-rich promoter binding protein 1	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20260402	MGI			
1313550	Gpbp1	GC-rich promoter binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313550	Gpbp1	GC-rich promoter binding protein 1	gene	MP:0011954	shortened PQ interval		IEA		N	RGD:5509061	20260402	MGI			
1313555	Plxnb2	plexin B2	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1313555	Plxnb2	plexin B2	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0000853	absent cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1313555	Plxnb2	plexin B2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1313555	Plxnb2	plexin B2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1313555	Plxnb2	plexin B2	gene	MP:0001756	abnormal urination		IEA		N	RGD:5509061	20160804	MGI			
1313555	Plxnb2	plexin B2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1313555	Plxnb2	plexin B2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1313555	Plxnb2	plexin B2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0004041	increased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20161201	MGI			PMID:25892012
1313555	Plxnb2	plexin B2	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:23175841
1313555	Plxnb2	plexin B2	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0006097	abnormal cerebellar lobule formation		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20161201	MGI			PMID:25892012
1313555	Plxnb2	plexin B2	gene	MP:0009941	abnormal olfactory bulb interneuron morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:23175841
1313555	Plxnb2	plexin B2	gene	MP:0009942	abnormal olfactory bulb granule cell morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:23175841
1313555	Plxnb2	plexin B2	gene	MP:0009943	abnormal olfactory bulb periglomerular cell morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:23175841
1313555	Plxnb2	plexin B2	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:23175841
1313555	Plxnb2	plexin B2	gene	MP:0009950	abnormal olfactory bulb internal plexiform layer morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:23175841
1313555	Plxnb2	plexin B2	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:23175841
1313555	Plxnb2	plexin B2	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1313555	Plxnb2	plexin B2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554007
1313555	Plxnb2	plexin B2	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0011760	abnormal ureteric bud tip morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0011761	abnormal ureteric bud trunk morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0011803	double kidney pelvis		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1313555	Plxnb2	plexin B2	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0015049	disorganized cerebellar granule layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:17409257
1313555	Plxnb2	plexin B2	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20161222	MGI			PMID:23175841
1313555	Plxnb2	plexin B2	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1313555	Plxnb2	plexin B2	gene	MP:0030956	abnormal neuronal precursor cell migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:23175841
1313555	Plxnb2	plexin B2	gene	MP:0030956	abnormal neuronal precursor cell migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:26579598
1313557	Msc	musculin	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0004234	abnormal masticatory muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0004236	absent masseter muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0004237	abnormal pterygoid muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0004238	absent pterygoid muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0004240	absent temporalis muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313557	Msc	musculin	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1313559	Mis18bp1	MIS18 binding protein 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20160804	MGI			
1313561	Cotl1	coactosin like F-actin binding protein 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1313561	Cotl1	coactosin like F-actin binding protein 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20170105	MGI			
1313561	Cotl1	coactosin like F-actin binding protein 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160811	MGI			
1313561	Cotl1	coactosin like F-actin binding protein 1	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
1313561	Cotl1	coactosin like F-actin binding protein 1	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1313565	Fam204a	family with sequence similarity 204, member A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1313571	Adck5	aarF domain containing kinase 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1313571	Adck5	aarF domain containing kinase 5	gene	MP:0002959	increased urine microalbumin level		IEA		N	RGD:5509061	20240523	MGI			
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0004473	absent nasal bone		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0004791	absent lower incisors		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0005367	renal/urinary system phenotype		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0005385	cardiovascular system phenotype		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0010234	abnormal vibrissa follicle morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20210128	MGI			
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0012725	small sebaceous gland		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0013370	anhidrosis		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0013458	decreased eccrine gland number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0030178	abnormal scalp morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313573	Kctd15	potassium channel tetramerisation domain containing 15	gene	MP:0031449	abnormal nasal cartilage morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1313576	Dnpep	aspartyl aminopeptidase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:29122955
1313576	Dnpep	aspartyl aminopeptidase	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1313576	Dnpep	aspartyl aminopeptidase	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1313582	Ppl	periplakin	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1313582	Ppl	periplakin	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1313582	Ppl	periplakin	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1313582	Ppl	periplakin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226441
1313582	Ppl	periplakin	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20181227	MGI			
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20210513	MGI			PMID:29853563
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20210513	MGI			PMID:29853563
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20141003	MGI			
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20210513	MGI			PMID:29853563
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20210513	MGI			PMID:29853563
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20210513	MGI			PMID:29853563
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20260219	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0013023	decreased Ly6C high monocyte number		IAGP		N	RGD:5509061	20210513	MGI			PMID:29853563
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0013799	abnormal intestinal goblet cell physiology		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0014201	abnormal intestinal epithelium physiology		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0014219	decreased intestinal mucosa thickness		IAGP		N	RGD:5509061	20210513	MGI			PMID:33219235
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0014413	decreased depression-related behavior		IEA		N	RGD:5509061	20240425	MGI			
1313584	Fam3d	FAM3 metabolism regulating signaling molecule D	gene	MP:0014431	increased chemokine level		IAGP		N	RGD:5509061	20260219	MGI			PMID:33219235
1313585	Rnf31	ring finger protein 31	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20230720	MGI			
1313585	Rnf31	ring finger protein 31	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221103	MGI			
1313585	Rnf31	ring finger protein 31	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1313585	Rnf31	ring finger protein 31	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20221103	MGI			
1313585	Rnf31	ring finger protein 31	gene	MP:0004940	abnormal B-1 B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20221103	MGI			
1313585	Rnf31	ring finger protein 31	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0008170	decreased B-1b cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23942237
1313585	Rnf31	ring finger protein 31	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313585	Rnf31	ring finger protein 31	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20221103	MGI			
1313588	Rgs17	regulator of G-protein signaling 17	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20260402	MGI			
1313588	Rgs17	regulator of G-protein signaling 17	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1313588	Rgs17	regulator of G-protein signaling 17	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1313588	Rgs17	regulator of G-protein signaling 17	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1313588	Rgs17	regulator of G-protein signaling 17	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20967545
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20967545
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0001123	dilated uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729625
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20967545
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729625
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729625
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20967545
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729625
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729625
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729625
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0008222	decreased hippocampal commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20967545
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20967545
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20967545
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729625
1313590	Cables1	CDK5 and Abl enzyme substrate 1	gene	MP:0009094	abnormal endometrial gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729625
1313592	Mrps28	mitochondrial ribosomal protein S28	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1313592	Mrps28	mitochondrial ribosomal protein S28	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1313597	Gnpda2	glucosamine-6-phosphate deaminase 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20221215	MGI			
1313598	B9d1	B9 protein domain 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1313598	B9d1	B9 protein domain 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20141003	MGI			
1313598	B9d1	B9 protein domain 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1313598	B9d1	B9 protein domain 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20141003	MGI			
1313598	B9d1	B9 protein domain 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1313598	B9d1	B9 protein domain 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0002138	abnormal hepatobiliary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1313598	B9d1	B9 protein domain 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1313598	B9d1	B9 protein domain 1	gene	MP:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0005316	abnormal response to tactile stimuli		IEA		N	RGD:5509061	20141003	MGI			
1313598	B9d1	B9 protein domain 1	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1313598	B9d1	B9 protein domain 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0011293	dilated nephron		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0011408	renal tubule hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20141120	MGI			PMID:21763481
1313598	B9d1	B9 protein domain 1	gene	MP:0013197	decreased embryonic cilium number		IAGP		N	RGD:5509061	20141120	MGI			PMID:21763481
1313601	Nt5dc2	5'-nucleotidase domain containing 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1313601	Nt5dc2	5'-nucleotidase domain containing 2	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20240523	MGI			
1313601	Nt5dc2	5'-nucleotidase domain containing 2	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1313601	Nt5dc2	5'-nucleotidase domain containing 2	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1313601	Nt5dc2	5'-nucleotidase domain containing 2	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20240523	MGI			
1313601	Nt5dc2	5'-nucleotidase domain containing 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1313601	Nt5dc2	5'-nucleotidase domain containing 2	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20220811	MGI			
1313601	Nt5dc2	5'-nucleotidase domain containing 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1313603	Pou5f2	POU domain class 5, transcription factor 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9207130
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210826	MGI			
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18439426
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548595
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18439426
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548595
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0008345	abnormal gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548595
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548595
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18439426
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0008399	abnormal alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18439426
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421850
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1313609	Ccl25	C-C motif chemokine ligand 25	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210826	MGI			
1313611	Hspa12a	heat shock protein family A (Hsp70) member 12A	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20210408	MGI			PMID:30455376
1313611	Hspa12a	heat shock protein family A (Hsp70) member 12A	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20210408	MGI			PMID:30742088
1313611	Hspa12a	heat shock protein family A (Hsp70) member 12A	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20210408	MGI			PMID:29530582
1313611	Hspa12a	heat shock protein family A (Hsp70) member 12A	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20210408	MGI			PMID:30742088
1313611	Hspa12a	heat shock protein family A (Hsp70) member 12A	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20210408	MGI			PMID:29530582
1313611	Hspa12a	heat shock protein family A (Hsp70) member 12A	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20210408	MGI			PMID:32332915
1313611	Hspa12a	heat shock protein family A (Hsp70) member 12A	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210408	MGI			PMID:30455376
1313611	Hspa12a	heat shock protein family A (Hsp70) member 12A	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20210408	MGI			PMID:30742088
1313611	Hspa12a	heat shock protein family A (Hsp70) member 12A	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:30455376
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:1641039
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2022963
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1641039
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1641039
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1641039
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:1641039
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:2022963
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:1641039
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:2022963
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:2022963
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:2022963
1313615	Tbce	tubulin-specific chaperone E	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000098	abnormal vomer bone morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0002200	abnormal brain ventricular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0004183	abnormal sympathetic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0004450	presphenoid bone hypoplasia		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0006302	abnormal ectomesenchyme morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0008581	disorganized photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20333246
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0008583	absent photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:22139371
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0030197	small nasal septum		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0030420	short basicranium		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0030443	abnormal cranial synchondrosis		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0030445	abnormal sphenooccipital synchondrosis		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0030447	abnormal presphenoid synchondrosis		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0030498	abnormal dental lamina morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:27170093
1313619	Arl6	ADP-ribosylation factor-like 6	gene	MP:0030966	decreased brain ependyma motile cilium number		IAGP		N	RGD:5509061	20190725	MGI			PMID:22139371
1313621	Hectd2	HECT domain E3 ubiquitin protein ligase 2	gene	MP:0000149	abnormal scapula morphology		IEA		N	RGD:5509061	20160421	MGI			
1313621	Hectd2	HECT domain E3 ubiquitin protein ligase 2	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20160811	MGI			
1313621	Hectd2	HECT domain E3 ubiquitin protein ligase 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230601	MGI			
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0005238	increased brain size		IEA		N	RGD:5509061	20230601	MGI			
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313624	Cfap91	cilia and flagella associated protein 91	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1313629	Fbl	fibrillarin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:14612397
1313629	Fbl	fibrillarin	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14612397
1313629	Fbl	fibrillarin	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14612397
1313633	Cdk14	cyclin dependent kinase 14	gene	MP:0002946	delayed axon extension		IAGP		N	RGD:5509061	20231123	MGI			PMID:37907898
1313633	Cdk14	cyclin dependent kinase 14	gene	MP:0010093	decreased circulating magnesium level		IEA		N	RGD:5509061	20181227	MGI			
1313635	Metap1	methionyl aminopeptidase 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20241121	MGI			
1313635	Metap1	methionyl aminopeptidase 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20250508	MGI			
1313635	Metap1	methionyl aminopeptidase 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1313635	Metap1	methionyl aminopeptidase 1	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20250508	MGI			
1313635	Metap1	methionyl aminopeptidase 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1313635	Metap1	methionyl aminopeptidase 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1313635	Metap1	methionyl aminopeptidase 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20241121	MGI			
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20120112	MGI			
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0003326	liver failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:14724179
1313637	Anapc2	anaphase promoting complex subunit 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724179
1313638	Ints2	integrator complex subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226392
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226392
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226392
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226392
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226392
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0008180	abnormal marginal zone B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226392
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226392
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226392
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0009328	delayed heart looping		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226392
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:30692166
1313643	Eps15	epidermal growth factor receptor pathway substrate 15	gene	MP:0030951	abnormal endocytosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313645	Rassf2	Ras association (RalGDS/AF-6) domain family member 2	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22227519
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20231207	MGI			
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20231207	MGI			
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20220519	MGI			
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20231207	MGI			
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313652	Nelfa	negative elongation factor complex member A, Whsc2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1313656	Ttk	Ttk protein kinase	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240919	MGI			
1313656	Ttk	Ttk protein kinase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21558374
1313656	Ttk	Ttk protein kinase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21558374
1313656	Ttk	Ttk protein kinase	gene	MP:0002718	abnormal inner cell mass morphology		IEA		N	RGD:5509061	20240919	MGI			
1313656	Ttk	Ttk protein kinase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21558374
1313656	Ttk	Ttk protein kinase	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21558374
1313656	Ttk	Ttk protein kinase	gene	MP:0009769	abnormal meiotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20141003	MGI			PMID:21558374
1313656	Ttk	Ttk protein kinase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1313656	Ttk	Ttk protein kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313656	Ttk	Ttk protein kinase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1313656	Ttk	Ttk protein kinase	gene	MP:0014444	enhanced polar body extrusion		IAGP		N	RGD:5509061	20240509	MGI			PMID:21558374
1313659	Nyap2	neuronal tyrosine-phophorylated phosphoinositide 3-kinase adaptor 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20180118	MGI			PMID:21946561
1313659	Nyap2	neuronal tyrosine-phophorylated phosphoinositide 3-kinase adaptor 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20180118	MGI			PMID:21946561
1313659	Nyap2	neuronal tyrosine-phophorylated phosphoinositide 3-kinase adaptor 2	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:21946561
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23142661
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220721	MGI			PMID:28319097
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20220721	MGI			PMID:28319097
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IEA		N	RGD:5509061	20141003	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20160421	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23142661
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0004975	absent regulatory T cells		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IEA		N	RGD:5509061	20141003	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20220721	MGI			PMID:28319097
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716941
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23142661
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20260402	MGI			
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0013583	salivary gland degeneration		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1313661	Satb1	special AT-rich sequence binding protein 1	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:28319097
1313663	Xpot	exportin, tRNA (nuclear export receptor for tRNAs)	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20161201	MGI			
1313663	Xpot	exportin, tRNA (nuclear export receptor for tRNAs)	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20161201	MGI			
1313663	Xpot	exportin, tRNA (nuclear export receptor for tRNAs)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1313663	Xpot	exportin, tRNA (nuclear export receptor for tRNAs)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961633
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562243
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562243
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562243
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961633
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562243
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961633
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961633
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0009600	hypergranulosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19145458
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961633
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562243
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562243
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961633
1313668	Supv3l1	suppressor of var1, 3-like 1 (S. cerevisiae)	gene	MP:0013192	decreased sebaceous gland number		IAGP		N	RGD:5509061	20141127	MGI			PMID:19145458
1313670	Upp1	uridine phosphorylase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077348
1313670	Upp1	uridine phosphorylase 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077348
1313670	Upp1	uridine phosphorylase 1	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077348
1313670	Upp1	uridine phosphorylase 1	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772079
1313670	Upp1	uridine phosphorylase 1	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077348
1313670	Upp1	uridine phosphorylase 1	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772079
1313670	Upp1	uridine phosphorylase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772079
1313670	Upp1	uridine phosphorylase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20251030	MGI			PMID:12077348
1313670	Upp1	uridine phosphorylase 1	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772079
1313670	Upp1	uridine phosphorylase 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772079
1313670	Upp1	uridine phosphorylase 1	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772079
1313670	Upp1	uridine phosphorylase 1	gene	MP:0009980	abnormal cerebellum dentate nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0011477	abnormal urine nucleoside level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772079
1313670	Upp1	uridine phosphorylase 1	gene	MP:0014958	decreased lung enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0014966	decreased heart enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:12077348
1313670	Upp1	uridine phosphorylase 1	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0014970	decreased muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0014972	decreased spleen enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313670	Upp1	uridine phosphorylase 1	gene	MP:0014975	decreased kidney enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313672	Lrfn3	leucine rich repeat and fibronectin type III domain containing 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1313672	Lrfn3	leucine rich repeat and fibronectin type III domain containing 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210520	MGI			
1313672	Lrfn3	leucine rich repeat and fibronectin type III domain containing 3	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20171116	MGI			PMID:27480238
1313672	Lrfn3	leucine rich repeat and fibronectin type III domain containing 3	gene	MP:0014375	increased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:27480238
1313672	Lrfn3	leucine rich repeat and fibronectin type III domain containing 3	gene	MP:0014382	increased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:27480238
1313672	Lrfn3	leucine rich repeat and fibronectin type III domain containing 3	gene	MP:0015054	increased synapse density		IAGP		N	RGD:5509061	20260813	MGI			PMID:27480238
1313672	Lrfn3	leucine rich repeat and fibronectin type III domain containing 3	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:27480238
1313674	Pax2	paired box 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11804780
1313674	Pax2	paired box 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0000044	absent organ of Corti		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11804780
1313674	Pax2	paired box 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
1313674	Pax2	paired box 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:22410172
1313674	Pax2	paired box 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22410172
1313674	Pax2	paired box 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0000899	abnormal corpora quadrigemina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22410172
1313674	Pax2	paired box 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1313674	Pax2	paired box 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0001948	vesicoureteral reflux		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1313674	Pax2	paired box 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0003146	absent cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003146	absent cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11804780
1313674	Pax2	paired box 2	gene	MP:0003146	absent cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0003146	absent cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:11804780
1313674	Pax2	paired box 2	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0003164	decreased posterior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0003166	decreased superior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0003169	abnormal scala media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
1313674	Pax2	paired box 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22410172
1313674	Pax2	paired box 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0003534	blind vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0003535	absent vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003535	absent vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0003557	absent vas deferens		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003557	absent vas deferens		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0003557	absent vas deferens		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0003558	absent uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003575	absent oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003575	absent oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0003584	bifid ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
1313674	Pax2	paired box 2	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003626	kidney medulla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0003626	kidney medulla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:11804780
1313674	Pax2	paired box 2	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
1313674	Pax2	paired box 2	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0004195	abnormal kidney calyx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0004195	abnormal kidney calyx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0004267	abnormal optic tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0004315	absent vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0004315	absent vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0004317	small vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0004330	abnormal vestibular saccular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0004369	absent utricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0004425	abnormal otolith organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
1313674	Pax2	paired box 2	gene	MP:0004717	absent cochlear nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0004727	absent epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0004727	absent epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0004729	absent efferent ductules of testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0004922	abnormal common crus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
1313674	Pax2	paired box 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15012626
1313674	Pax2	paired box 2	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0006106	absent tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0006426	Mullerian duct degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0006426	Mullerian duct degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0008065	short endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0008065	short endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0008066	small endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0008307	short scala media		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0008487	abnormal mesonephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15242798
1313674	Pax2	paired box 2	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1313674	Pax2	paired box 2	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0009074	Wolffian duct degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0009074	Wolffian duct degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0009075	rudimentary Wolffian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0009076	rudimentary Mullerian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15012626
1313674	Pax2	paired box 2	gene	MP:0009167	increased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15012626
1313674	Pax2	paired box 2	gene	MP:0009215	absent uterine horn		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0009262	absent semicircular canal ampulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0009771	absent optic chiasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0009846	abnormal neural crest morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0010118	abnormal intermediate mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0010716	optic disk coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1313674	Pax2	paired box 2	gene	MP:0010717	optic nerve coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0010980	ectopic ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0010986	abnormal mesonephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15012626
1313674	Pax2	paired box 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22410172
1313674	Pax2	paired box 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047028
1313674	Pax2	paired box 2	gene	MP:0011238	abnormal inner ear development		IAGP		N	RGD:5509061	20240822	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22410172
1313674	Pax2	paired box 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22410172
1313674	Pax2	paired box 2	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0011360	kidney cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0011365	small metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0011366	absent metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:12435636
1313674	Pax2	paired box 2	gene	MP:0011366	absent metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575306
1313674	Pax2	paired box 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587573
1313674	Pax2	paired box 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14603255
1313674	Pax2	paired box 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16609680
1313674	Pax2	paired box 2	gene	MP:0011382	abnormal kidney lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22410172
1313674	Pax2	paired box 2	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881463
1313674	Pax2	paired box 2	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:22410172
1313674	Pax2	paired box 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943028
1313674	Pax2	paired box 2	gene	MP:0012533	uveal coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313674	Pax2	paired box 2	gene	MP:0012535	abnormal optic fissure closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934015
1313674	Pax2	paired box 2	gene	MP:0012535	abnormal optic fissure closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951055
1313674	Pax2	paired box 2	gene	MP:0012536	delayed optic fissure closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221250
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484451
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:16511604
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20805469
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20805469
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000469	abnormal esophageal squamous epithelium morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:25652409
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:25652409
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001221	epidermal atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421363
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439468
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20805469
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421363
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484451
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16511604
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484451
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16511604
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16511604
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421363
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20805469
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16511604
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:20805469
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0004548	dilated esophagus		IAGP		N	RGD:5509061	20160407	MGI			PMID:25652409
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0004675	rib fractures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0004675	rib fractures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421363
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0004675	rib fractures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439468
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20805469
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20805469
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15608054
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484451
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421363
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005567	decreased circulating total protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421363
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20805469
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0009480	distended cecum		IAGP		N	RGD:5509061	20160407	MGI			PMID:25652409
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0009878	decreased susceptibility to bone fracture		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439468
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0011009	increased circulating glutamate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439468
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20181129	MGI			PMID:11923874
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0011570	esophageal achalasia		IAGP		N	RGD:5509061	20160407	MGI			PMID:25652409
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0021188	decreased bone mineral density of presacral vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0030082	long lower incisors		IAGP		N	RGD:5509061	20171005	MGI			PMID:12235369
1313678	Zmpste24	zinc metallopeptidase, STE24	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:12235369
1313680	Cnnm4	cyclin M4	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:24339795
1313680	Cnnm4	cyclin M4	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:24339795
1313680	Cnnm4	cyclin M4	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20150618	MGI			PMID:24339795
1313680	Cnnm4	cyclin M4	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20210429	MGI			PMID:28033128
1313680	Cnnm4	cyclin M4	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20210429	MGI			PMID:28033128
1313680	Cnnm4	cyclin M4	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20150618	MGI			PMID:24339795
1313680	Cnnm4	cyclin M4	gene	MP:0010093	decreased circulating magnesium level		IAGP		N	RGD:5509061	20150618	MGI			PMID:24339795
1313680	Cnnm4	cyclin M4	gene	MP:0010093	decreased circulating magnesium level		IAGP		N	RGD:5509061	20210429	MGI			PMID:28033128
1313680	Cnnm4	cyclin M4	gene	MP:0011436	decreased urine magnesium level		IAGP		N	RGD:5509061	20150618	MGI			PMID:24339795
1313680	Cnnm4	cyclin M4	gene	MP:0013129	abnormal tooth color		IAGP		N	RGD:5509061	20150618	MGI			PMID:24339795
1313680	Cnnm4	cyclin M4	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20171221	MGI			PMID:24339795
1313683	Rpl38	ribosomal protein L38	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0000267	abnormal heart development		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:465735
1313683	Rpl38	ribosomal protein L38	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:9615218
1313683	Rpl38	ribosomal protein L38	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0000819	abnormal olfactory bulb morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0000930	wavy neural tube		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7373273
1313683	Rpl38	ribosomal protein L38	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:7373273
1313683	Rpl38	ribosomal protein L38	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:465735
1313683	Rpl38	ribosomal protein L38	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0002237	abnormal nasal cavity morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:7373273
1313683	Rpl38	ribosomal protein L38	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2980249
1313683	Rpl38	ribosomal protein L38	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0003050	abnormal sacral vertebrae morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:465735
1313683	Rpl38	ribosomal protein L38	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0003072	abnormal metatarsal bone morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0003073	abnormal metacarpal bone morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0003109	short femur		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0003208	abnormal neuromere morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0003330	abnormal auditory tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:465735
1313683	Rpl38	ribosomal protein L38	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7373273
1313683	Rpl38	ribosomal protein L38	gene	MP:0004229	abnormal embryonic erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:465735
1313683	Rpl38	ribosomal protein L38	gene	MP:0004322	abnormal sternebra morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0004351	short humerus		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0004355	short radius		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0004479	abnormal oval window morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0004480	abnormal round window morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004600	abnormal vertebral transverse process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004604	abnormal vertebral pedicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004605	abnormal vertebral lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0004614	caudal vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0004651	increased thoracic vertebrae number		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0004652	small caudal vertebrae		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0004653	absent caudal vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0004686	decreased length of long bones		IEA		N	RGD:5509061	20141003	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7373273
1313683	Rpl38	ribosomal protein L38	gene	MP:0004963	abnormal blastocoele morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7373273
1313683	Rpl38	ribosomal protein L38	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0005225	abnormal vertebrae development		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20111116	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19011615
1313683	Rpl38	ribosomal protein L38	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0008830	abnormal nucleolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7373273
1313683	Rpl38	ribosomal protein L38	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7373273
1313683	Rpl38	ribosomal protein L38	gene	MP:0010082	sternebra fusion		IEA		N	RGD:5509061	20141003	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9615218
1313683	Rpl38	ribosomal protein L38	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889952
1313683	Rpl38	ribosomal protein L38	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779008
1313683	Rpl38	ribosomal protein L38	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995757
1313683	Rpl38	ribosomal protein L38	gene	MP:0011103	embryonic lethality at implantation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7373273
1313683	Rpl38	ribosomal protein L38	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21062742
1313683	Rpl38	ribosomal protein L38	gene	MP:0012284	increased sternebra number		IEA		N	RGD:5509061	20141003	MGI			
1313683	Rpl38	ribosomal protein L38	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:465735
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220811	MGI			
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:28407788
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20220811	MGI			
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0009164	exocrine pancreas atrophy		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28407788
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220811	MGI			
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220811	MGI			
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220811	MGI			
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20250515	MGI			PMID:39499645
1313684	Polr3a	polymerase (RNA) III (DNA directed) polypeptide A	gene	MP:0031496	motor developmental delay		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1313688	Kif9	kinesin family member 9	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1313688	Kif9	kinesin family member 9	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1313688	Kif9	kinesin family member 9	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1313688	Kif9	kinesin family member 9	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20211209	MGI			PMID:32072696
1313688	Kif9	kinesin family member 9	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1313688	Kif9	kinesin family member 9	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20201022	MGI			
1313688	Kif9	kinesin family member 9	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20211209	MGI			PMID:32072696
1313688	Kif9	kinesin family member 9	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20211209	MGI			PMID:32072696
1313688	Kif9	kinesin family member 9	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20211209	MGI			PMID:32072696
1313688	Kif9	kinesin family member 9	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20211209	MGI			PMID:32072696
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17008428
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0003269	colon polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717065
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1313690	Mcm2	minichromosome maintenance complex component 2	gene	MP:0014127	increased thymoma incidence		IAGP		N	RGD:5509061	20160317	MGI			PMID:17717065
1313692	Swap70	SWA-70 protein	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11500831
1313692	Swap70	SWA-70 protein	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11500831
1313692	Swap70	SWA-70 protein	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11500831
1313692	Swap70	SWA-70 protein	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11500831
1313695	Itgb2	integrin beta 2	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172402
1313695	Itgb2	integrin beta 2	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172402
1313695	Itgb2	integrin beta 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1313695	Itgb2	integrin beta 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8101543
1313695	Itgb2	integrin beta 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
1313695	Itgb2	integrin beta 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1313695	Itgb2	integrin beta 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23823319
1313695	Itgb2	integrin beta 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1313695	Itgb2	integrin beta 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8101543
1313695	Itgb2	integrin beta 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819024
1313695	Itgb2	integrin beta 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23823319
1313695	Itgb2	integrin beta 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819024
1313695	Itgb2	integrin beta 2	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819024
1313695	Itgb2	integrin beta 2	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819024
1313695	Itgb2	integrin beta 2	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982899
1313695	Itgb2	integrin beta 2	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18390736
1313695	Itgb2	integrin beta 2	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819024
1313695	Itgb2	integrin beta 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
1313695	Itgb2	integrin beta 2	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819024
1313695	Itgb2	integrin beta 2	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766082
1313695	Itgb2	integrin beta 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
1313695	Itgb2	integrin beta 2	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20200116	MGI			PMID:16505059
1313695	Itgb2	integrin beta 2	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819024
1313695	Itgb2	integrin beta 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8101543
1313695	Itgb2	integrin beta 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
1313695	Itgb2	integrin beta 2	gene	MP:0002145	abnormal T cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711877
1313695	Itgb2	integrin beta 2	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8101543
1313695	Itgb2	integrin beta 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451854
1313695	Itgb2	integrin beta 2	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585877
1313695	Itgb2	integrin beta 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23823319
1313695	Itgb2	integrin beta 2	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0002497	increased IgE level		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0002606	increased basophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
1313695	Itgb2	integrin beta 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1313695	Itgb2	integrin beta 2	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819024
1313695	Itgb2	integrin beta 2	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0003434	decreased susceptibility to induced choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766082
1313695	Itgb2	integrin beta 2	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18390736
1313695	Itgb2	integrin beta 2	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1313695	Itgb2	integrin beta 2	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172402
1313695	Itgb2	integrin beta 2	gene	MP:0003813	abnormal hair follicle dermal papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0003884	decreased macrophage cell number		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1313695	Itgb2	integrin beta 2	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1313695	Itgb2	integrin beta 2	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8101543
1313695	Itgb2	integrin beta 2	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23823319
1313695	Itgb2	integrin beta 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23823319
1313695	Itgb2	integrin beta 2	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
1313695	Itgb2	integrin beta 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1313695	Itgb2	integrin beta 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1313695	Itgb2	integrin beta 2	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210787
1313695	Itgb2	integrin beta 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23823319
1313695	Itgb2	integrin beta 2	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
1313695	Itgb2	integrin beta 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231732
1313695	Itgb2	integrin beta 2	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0008053	abnormal NK cell differentiation		IEA		N	RGD:5509061	20111116	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1313695	Itgb2	integrin beta 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1313695	Itgb2	integrin beta 2	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1313695	Itgb2	integrin beta 2	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23823319
1313695	Itgb2	integrin beta 2	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23823319
1313695	Itgb2	integrin beta 2	gene	MP:0008127	decreased dendritic cell number		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20190418	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:16505059
1313695	Itgb2	integrin beta 2	gene	MP:0008564	increased interferon-beta secretion		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0008567	decreased interferon-gamma secretion		IEA		N	RGD:5509061	20111116	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0008623	increased circulating interleukin-3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634077
1313695	Itgb2	integrin beta 2	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228023
1313695	Itgb2	integrin beta 2	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819024
1313695	Itgb2	integrin beta 2	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451854
1313695	Itgb2	integrin beta 2	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8101543
1313695	Itgb2	integrin beta 2	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700894
1313695	Itgb2	integrin beta 2	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172402
1313695	Itgb2	integrin beta 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653089
1313695	Itgb2	integrin beta 2	gene	MP:0013280	abnormal cytotoxic T cell cytolysis		IEA		N	RGD:5509061	20181011	MGI			
1313695	Itgb2	integrin beta 2	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:16172402
1313695	Itgb2	integrin beta 2	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:16172402
1313695	Itgb2	integrin beta 2	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:16172402
1313695	Itgb2	integrin beta 2	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20181011	MGI			
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0001128	ovary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0006361	abnormal female germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22771120
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0014619	absent spermatogonia		IAGP		N	RGD:5509061	20250213	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0031020	premature ovarian failure		IAGP		N	RGD:5509061	20200130	MGI			PMID:21987787
1313697	Mcm9	minichromosome maintenance 9 homologous recombination repair factor	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:22771120
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20150122	MGI			PMID:24733397
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20150122	MGI			PMID:24733397
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20150122	MGI			PMID:24733397
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20150122	MGI			PMID:24733397
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0003889	enhanced sensorimotor gating		IEA		N	RGD:5509061	20141003	MGI			
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0005444	abnormal retinol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0005444	abnormal retinol metabolism		IAGP		N	RGD:5509061	20150122	MGI			PMID:24733397
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20150122	MGI			PMID:24733397
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150122	MGI			PMID:24733397
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005908
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1313700	Dhrs3	dehydrogenase/reductase 3	gene	MP:0011234	abnormal retinol level		IAGP		N	RGD:5509061	20150122	MGI			PMID:24733397
1313702	Col6a2	collagen, type VI, alpha 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20180215	MGI			
1313702	Col6a2	collagen, type VI, alpha 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160114	MGI			
1313707	Rag2	recombination activating gene 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20260806	MGI			PMID:19584867
1313707	Rag2	recombination activating gene 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10614672
1313707	Rag2	recombination activating gene 2	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871643
1313707	Rag2	recombination activating gene 2	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10614672
1313707	Rag2	recombination activating gene 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871643
1313707	Rag2	recombination activating gene 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884426
1313707	Rag2	recombination activating gene 2	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1313707	Rag2	recombination activating gene 2	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1313707	Rag2	recombination activating gene 2	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982764
1313707	Rag2	recombination activating gene 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1313707	Rag2	recombination activating gene 2	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618483
1313707	Rag2	recombination activating gene 2	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843678
1313707	Rag2	recombination activating gene 2	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1313707	Rag2	recombination activating gene 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10523604
1313707	Rag2	recombination activating gene 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618483
1313707	Rag2	recombination activating gene 2	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442925
1313707	Rag2	recombination activating gene 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10610182
1313707	Rag2	recombination activating gene 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10610182
1313707	Rag2	recombination activating gene 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20151217	MGI			PMID:26099023
1313707	Rag2	recombination activating gene 2	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20151217	MGI			PMID:26099023
1313707	Rag2	recombination activating gene 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10614672
1313707	Rag2	recombination activating gene 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20151112	MGI			PMID:22089030
1313707	Rag2	recombination activating gene 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676849
1313707	Rag2	recombination activating gene 2	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1313707	Rag2	recombination activating gene 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1313707	Rag2	recombination activating gene 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791433
1313707	Rag2	recombination activating gene 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23661644
1313707	Rag2	recombination activating gene 2	gene	MP:0001800	abnormal humoral immune response		IEA		N	RGD:5509061	20141003	MGI			
1313707	Rag2	recombination activating gene 2	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618483
1313707	Rag2	recombination activating gene 2	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1313707	Rag2	recombination activating gene 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618483
1313707	Rag2	recombination activating gene 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15197172
1313707	Rag2	recombination activating gene 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597497
1313707	Rag2	recombination activating gene 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9341770
1313707	Rag2	recombination activating gene 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9285410
1313707	Rag2	recombination activating gene 2	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24021673
1313707	Rag2	recombination activating gene 2	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10610182
1313707	Rag2	recombination activating gene 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20160505	MGI			PMID:22264274
1313707	Rag2	recombination activating gene 2	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349429
1313707	Rag2	recombination activating gene 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349429
1313707	Rag2	recombination activating gene 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
1313707	Rag2	recombination activating gene 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584189
1313707	Rag2	recombination activating gene 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20161222	MGI			PMID:26753883
1313707	Rag2	recombination activating gene 2	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20161222	MGI			PMID:26753883
1313707	Rag2	recombination activating gene 2	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397239
1313707	Rag2	recombination activating gene 2	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1313707	Rag2	recombination activating gene 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
1313707	Rag2	recombination activating gene 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584189
1313707	Rag2	recombination activating gene 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151217	MGI			PMID:26099023
1313707	Rag2	recombination activating gene 2	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871643
1313707	Rag2	recombination activating gene 2	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186486
1313707	Rag2	recombination activating gene 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238603
1313707	Rag2	recombination activating gene 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776904
1313707	Rag2	recombination activating gene 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1313707	Rag2	recombination activating gene 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1313707	Rag2	recombination activating gene 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485655
1313707	Rag2	recombination activating gene 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12433370
1313707	Rag2	recombination activating gene 2	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12433370
1313707	Rag2	recombination activating gene 2	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15021880
1313707	Rag2	recombination activating gene 2	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
1313707	Rag2	recombination activating gene 2	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15021880
1313707	Rag2	recombination activating gene 2	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17579027
1313707	Rag2	recombination activating gene 2	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9285410
1313707	Rag2	recombination activating gene 2	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19084435
1313707	Rag2	recombination activating gene 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951970
1313707	Rag2	recombination activating gene 2	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9285410
1313707	Rag2	recombination activating gene 2	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239447
1313707	Rag2	recombination activating gene 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539897
1313707	Rag2	recombination activating gene 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871643
1313707	Rag2	recombination activating gene 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0002465	abnormal eosinophil physiology		IAGP		N	RGD:5509061	20170824	MGI			PMID:25398911
1313707	Rag2	recombination activating gene 2	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20151217	MGI			PMID:26099023
1313707	Rag2	recombination activating gene 2	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17081782
1313707	Rag2	recombination activating gene 2	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1313707	Rag2	recombination activating gene 2	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20260806	MGI			PMID:19584867
1313707	Rag2	recombination activating gene 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239447
1313707	Rag2	recombination activating gene 2	gene	MP:0003080	increased natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1313707	Rag2	recombination activating gene 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262827
1313707	Rag2	recombination activating gene 2	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1313707	Rag2	recombination activating gene 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20161222	MGI			PMID:26753883
1313707	Rag2	recombination activating gene 2	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676849
1313707	Rag2	recombination activating gene 2	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676849
1313707	Rag2	recombination activating gene 2	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0003454	erythroderma		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0003504	thyroid gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9285410
1313707	Rag2	recombination activating gene 2	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087873
1313707	Rag2	recombination activating gene 2	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
1313707	Rag2	recombination activating gene 2	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442925
1313707	Rag2	recombination activating gene 2	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641034
1313707	Rag2	recombination activating gene 2	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15383179
1313707	Rag2	recombination activating gene 2	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
1313707	Rag2	recombination activating gene 2	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587764
1313707	Rag2	recombination activating gene 2	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17873878
1313707	Rag2	recombination activating gene 2	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483694
1313707	Rag2	recombination activating gene 2	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587764
1313707	Rag2	recombination activating gene 2	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1313707	Rag2	recombination activating gene 2	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22089030
1313707	Rag2	recombination activating gene 2	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10614672
1313707	Rag2	recombination activating gene 2	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843678
1313707	Rag2	recombination activating gene 2	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1313707	Rag2	recombination activating gene 2	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751756
1313707	Rag2	recombination activating gene 2	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20260806	MGI			PMID:19584867
1313707	Rag2	recombination activating gene 2	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17873878
1313707	Rag2	recombination activating gene 2	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20170824	MGI			PMID:25398911
1313707	Rag2	recombination activating gene 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24021673
1313707	Rag2	recombination activating gene 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618483
1313707	Rag2	recombination activating gene 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871643
1313707	Rag2	recombination activating gene 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15021880
1313707	Rag2	recombination activating gene 2	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164958
1313707	Rag2	recombination activating gene 2	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163198
1313707	Rag2	recombination activating gene 2	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9341770
1313707	Rag2	recombination activating gene 2	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751756
1313707	Rag2	recombination activating gene 2	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15197172
1313707	Rag2	recombination activating gene 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15197172
1313707	Rag2	recombination activating gene 2	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843678
1313707	Rag2	recombination activating gene 2	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442925
1313707	Rag2	recombination activating gene 2	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
1313707	Rag2	recombination activating gene 2	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597497
1313707	Rag2	recombination activating gene 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618483
1313707	Rag2	recombination activating gene 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18923423
1313707	Rag2	recombination activating gene 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1313707	Rag2	recombination activating gene 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653054
1313707	Rag2	recombination activating gene 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9285410
1313707	Rag2	recombination activating gene 2	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9285410
1313707	Rag2	recombination activating gene 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641034
1313707	Rag2	recombination activating gene 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1313707	Rag2	recombination activating gene 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10614672
1313707	Rag2	recombination activating gene 2	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706337
1313707	Rag2	recombination activating gene 2	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9341770
1313707	Rag2	recombination activating gene 2	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9285410
1313707	Rag2	recombination activating gene 2	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17081782
1313707	Rag2	recombination activating gene 2	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15383179
1313707	Rag2	recombination activating gene 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498815
1313707	Rag2	recombination activating gene 2	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1313707	Rag2	recombination activating gene 2	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:17081782
1313707	Rag2	recombination activating gene 2	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951970
1313707	Rag2	recombination activating gene 2	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262803
1313707	Rag2	recombination activating gene 2	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262827
1313707	Rag2	recombination activating gene 2	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141211	MGI			PMID:24633240
1313707	Rag2	recombination activating gene 2	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20210506	MGI			PMID:32381589
1313707	Rag2	recombination activating gene 2	gene	MP:0005673	decreased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20141003	MGI			PMID:24021673
1313707	Rag2	recombination activating gene 2	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10610182
1313707	Rag2	recombination activating gene 2	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363300
1313707	Rag2	recombination activating gene 2	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15021880
1313707	Rag2	recombination activating gene 2	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12586624
1313707	Rag2	recombination activating gene 2	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19084435
1313707	Rag2	recombination activating gene 2	gene	MP:0008046	absent NK cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12586624
1313707	Rag2	recombination activating gene 2	gene	MP:0008046	absent NK cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12586624
1313707	Rag2	recombination activating gene 2	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12586624
1313707	Rag2	recombination activating gene 2	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17918199
1313707	Rag2	recombination activating gene 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843678
1313707	Rag2	recombination activating gene 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
1313707	Rag2	recombination activating gene 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1313707	Rag2	recombination activating gene 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24021673
1313707	Rag2	recombination activating gene 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9285410
1313707	Rag2	recombination activating gene 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9341770
1313707	Rag2	recombination activating gene 2	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843678
1313707	Rag2	recombination activating gene 2	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17918199
1313707	Rag2	recombination activating gene 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
1313707	Rag2	recombination activating gene 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24021673
1313707	Rag2	recombination activating gene 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9341770
1313707	Rag2	recombination activating gene 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9341770
1313707	Rag2	recombination activating gene 2	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1313707	Rag2	recombination activating gene 2	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597497
1313707	Rag2	recombination activating gene 2	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1313707	Rag2	recombination activating gene 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509509
1313707	Rag2	recombination activating gene 2	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12433370
1313707	Rag2	recombination activating gene 2	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871643
1313707	Rag2	recombination activating gene 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0008213	absent immature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602643
1313707	Rag2	recombination activating gene 2	gene	MP:0008348	absent gamma-delta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17617584
1313707	Rag2	recombination activating gene 2	gene	MP:0008356	abnormal gamma-delta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531919
1313707	Rag2	recombination activating gene 2	gene	MP:0008464	absent peripheral lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:24021673
1313707	Rag2	recombination activating gene 2	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595226
1313707	Rag2	recombination activating gene 2	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1313707	Rag2	recombination activating gene 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20260402	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20260212	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19084435
1313707	Rag2	recombination activating gene 2	gene	MP:0008588	abnormal circulating interleukin level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22089030
1313707	Rag2	recombination activating gene 2	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20151112	MGI			PMID:22089030
1313707	Rag2	recombination activating gene 2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641034
1313707	Rag2	recombination activating gene 2	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0008755	abnormal immunoglobulin V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:1547487
1313707	Rag2	recombination activating gene 2	gene	MP:0008755	abnormal immunoglobulin V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349429
1313707	Rag2	recombination activating gene 2	gene	MP:0008759	abnormal T cell receptor delta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17579065
1313707	Rag2	recombination activating gene 2	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9285410
1313707	Rag2	recombination activating gene 2	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1313707	Rag2	recombination activating gene 2	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20260806	MGI			PMID:19584867
1313707	Rag2	recombination activating gene 2	gene	MP:0009515	increased gastrointestinal stromal tumor incidence		IAGP		N	RGD:5509061	20161222	MGI			PMID:26753883
1313707	Rag2	recombination activating gene 2	gene	MP:0009540	absent Hassall's corpuscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0009624	small inguinal lymph nodes		IAGP		N	RGD:5509061	20170713	MGI			PMID:17476358
1313707	Rag2	recombination activating gene 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20639491
1313707	Rag2	recombination activating gene 2	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082625
1313707	Rag2	recombination activating gene 2	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12433370
1313707	Rag2	recombination activating gene 2	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20161222	MGI			PMID:26753883
1313707	Rag2	recombination activating gene 2	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363300
1313707	Rag2	recombination activating gene 2	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20160505	MGI			PMID:22264274
1313707	Rag2	recombination activating gene 2	gene	MP:0010365	increased thymus tumor incidence		IAGP		N	RGD:5509061	20161222	MGI			PMID:26753883
1313707	Rag2	recombination activating gene 2	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982764
1313707	Rag2	recombination activating gene 2	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20260806	MGI			PMID:19584867
1313707	Rag2	recombination activating gene 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1313707	Rag2	recombination activating gene 2	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368836
1313707	Rag2	recombination activating gene 2	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20260806	MGI			PMID:19584867
1313707	Rag2	recombination activating gene 2	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160304	MGI			PMID:22089030
1313707	Rag2	recombination activating gene 2	gene	MP:0020184	abnormal susceptibility to parasitic infection		IAGP		N	RGD:5509061	20170824	MGI			PMID:25398911
1313707	Rag2	recombination activating gene 2	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:24021673
1313707	Rag2	recombination activating gene 2	gene	MP:0030011	small cervical lymph nodes		IAGP		N	RGD:5509061	20170713	MGI			PMID:17476358
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230601	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20230601	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0003402	decreased liver weight		IEA		N	RGD:5509061	20241121	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20150716	MGI			PMID:24958848
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20230119	MGI			
1313709	Fgd5	FYVE, RhoGEF and PH domain containing 5	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0001191	abnormal skin condition		IEA		N	RGD:5509061	20160804	MGI			
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0002791	steatorrhea		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0020151	abnormal circulating non-HDL cholesterol level		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313711	Sar1b	secretion associated Ras related GTPase 1B	gene	MP:0020868	decreased lipogenesis		IAGP		N	RGD:5509061	20220908	MGI			PMID:33964306
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20240523	MGI			
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230119	MGI			
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20211021	MGI			PMID:32428862
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20211021	MGI			PMID:32428862
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20211021	MGI			PMID:32428862
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20211021	MGI			PMID:32428862
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20211021	MGI			PMID:32428862
1313713	Slc37a2	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0003794	delayed somite formation		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0003891	increased allantois apoptosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0004559	small allantois		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0011200	abnormal extraembryonic coelom morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0020515	abnormal visceral yolk sac endoderm morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313714	Pagr1a	PAXIP1 associated glutamate rich protein 1A	gene	MP:0020517	abnormal visceral yolk sac physiology		IAGP		N	RGD:5509061	20180712	MGI			PMID:24633704
1313716	Evx2	even-skipped homeobox 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1313716	Evx2	even-skipped homeobox 2	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1313716	Evx2	even-skipped homeobox 2	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1313716	Evx2	even-skipped homeobox 2	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1313716	Evx2	even-skipped homeobox 2	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1313716	Evx2	even-skipped homeobox 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1313716	Evx2	even-skipped homeobox 2	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1313716	Evx2	even-skipped homeobox 2	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1313716	Evx2	even-skipped homeobox 2	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313716	Evx2	even-skipped homeobox 2	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1313718	Adgre5	adhesion G protein-coupled receptor E5	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158902
1313718	Adgre5	adhesion G protein-coupled receptor E5	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18941248
1313718	Adgre5	adhesion G protein-coupled receptor E5	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1313718	Adgre5	adhesion G protein-coupled receptor E5	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158902
1313718	Adgre5	adhesion G protein-coupled receptor E5	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158902
1313722	Gba2	glucosidase beta 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20160804	MGI			
1313722	Gba2	glucosidase beta 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0009257	dilated seminiferous tubule		IAGP		N	RGD:5509061	20220922	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:17080196
1313722	Gba2	glucosidase beta 2	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:17080196
1313724	U2af1l4	U2 small nuclear RNA auxiliary factor 1-like 4	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20171012	MGI			PMID:24837677
1313728	Ephb3	Eph receptor B3	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539827
1313728	Ephb3	Eph receptor B3	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143520
1313728	Ephb3	Eph receptor B3	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914164
1313728	Ephb3	Eph receptor B3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12971893
1313728	Ephb3	Eph receptor B3	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0002946	delayed axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539827
1313728	Ephb3	Eph receptor B3	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1313728	Ephb3	Eph receptor B3	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143520
1313728	Ephb3	Eph receptor B3	gene	MP:0004267	abnormal optic tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12971893
1313728	Ephb3	Eph receptor B3	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0004775	abnormal vestibular dark cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777604
1313728	Ephb3	Eph receptor B3	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777604
1313728	Ephb3	Eph receptor B3	gene	MP:0004885	abnormal endolymph physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1313728	Ephb3	Eph receptor B3	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1313728	Ephb3	Eph receptor B3	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182796
1313728	Ephb3	Eph receptor B3	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21847105
1313728	Ephb3	Eph receptor B3	gene	MP:0006389	abnormal vestibular endolymph physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1313728	Ephb3	Eph receptor B3	gene	MP:0006391	abnormal vestibular endolymph ionic homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1313728	Ephb3	Eph receptor B3	gene	MP:0008066	small endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839360
1313728	Ephb3	Eph receptor B3	gene	MP:0008960	abnormal axon pruning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182796
1313728	Ephb3	Eph receptor B3	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914164
1313728	Ephb3	Eph receptor B3	gene	MP:0014077	ectopic Paneth cells		IAGP		N	RGD:5509061	20160310	MGI			PMID:19914164
1313730	Pfdn1	prefoldin 1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1313730	Pfdn1	prefoldin 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20220811	MGI			
1313730	Pfdn1	prefoldin 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1313730	Pfdn1	prefoldin 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20220811	MGI			
1313730	Pfdn1	prefoldin 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210128	MGI			
1313730	Pfdn1	prefoldin 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0001872	sinus inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1313730	Pfdn1	prefoldin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20210128	MGI			
1313730	Pfdn1	prefoldin 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566413
1313730	Pfdn1	prefoldin 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313731	Ccdc30	coiled-coil domain containing 30	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1313733	Nop14	NOP14 nucleolar protein	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20260402	MGI			
1313733	Nop14	NOP14 nucleolar protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1313734	Otud4	OTU domain containing 4	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
1313734	Otud4	OTU domain containing 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313736	Adamtsl5	ADAMTS-like 5	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0001413	abnormal response to new environment		IEA		N	RGD:5509061	20200402	MGI			
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20201015	MGI			PMID:25751059
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20201015	MGI			PMID:25751059
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20201015	MGI			PMID:25751059
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20201015	MGI			PMID:25751059
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20150625	MGI			
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20201015	MGI			PMID:25751059
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:25751059
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20201015	MGI			PMID:25751059
1313738	Adgrb1	adhesion G protein-coupled receptor B1	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:25751059
1313740	Shcbp1l	Shc SH2-domain binding protein 1-like	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20160317	MGI			PMID:24557841
1313740	Shcbp1l	Shc SH2-domain binding protein 1-like	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20160317	MGI			PMID:24557841
1313740	Shcbp1l	Shc SH2-domain binding protein 1-like	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20160317	MGI			PMID:24557841
1313740	Shcbp1l	Shc SH2-domain binding protein 1-like	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20160317	MGI			PMID:24557841
1313740	Shcbp1l	Shc SH2-domain binding protein 1-like	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:24557841
1313740	Shcbp1l	Shc SH2-domain binding protein 1-like	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:24557841
1313740	Shcbp1l	Shc SH2-domain binding protein 1-like	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:24557841
1313742	Sh3tc1	SH3 domain and tetratricopeptide repeats 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1313742	Sh3tc1	SH3 domain and tetratricopeptide repeats 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1313742	Sh3tc1	SH3 domain and tetratricopeptide repeats 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1313742	Sh3tc1	SH3 domain and tetratricopeptide repeats 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20211021	MGI			
1313742	Sh3tc1	SH3 domain and tetratricopeptide repeats 1	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20210128	MGI			
1313742	Sh3tc1	SH3 domain and tetratricopeptide repeats 1	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20211021	MGI			
1313742	Sh3tc1	SH3 domain and tetratricopeptide repeats 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1313742	Sh3tc1	SH3 domain and tetratricopeptide repeats 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1313742	Sh3tc1	SH3 domain and tetratricopeptide repeats 1	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20210128	MGI			
1313744	Smarce1	SWI/SNF related BAF chromatin remodeling complex subunit E1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1313744	Smarce1	SWI/SNF related BAF chromatin remodeling complex subunit E1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1313744	Smarce1	SWI/SNF related BAF chromatin remodeling complex subunit E1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1313744	Smarce1	SWI/SNF related BAF chromatin remodeling complex subunit E1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23198860
1313744	Smarce1	SWI/SNF related BAF chromatin remodeling complex subunit E1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1313744	Smarce1	SWI/SNF related BAF chromatin remodeling complex subunit E1	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1313744	Smarce1	SWI/SNF related BAF chromatin remodeling complex subunit E1	gene	MP:0014134	abnormal embryo morphology		IEA		N	RGD:5509061	20240926	MGI			
1313744	Smarce1	SWI/SNF related BAF chromatin remodeling complex subunit E1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1313746	Spns1	SPNS lysolipid transporter 1, lysophospholipid	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20160804	MGI			
1313746	Spns1	SPNS lysolipid transporter 1, lysophospholipid	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0001214	skin hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18256672
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002451	abnormal macrophage physiology		IEA		N	RGD:5509061	20141003	MGI			
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002607	decreased basophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10990461
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:10990461
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10990461
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0004971	dermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18256672
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18256672
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18256672
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18256672
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18256672
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10990461
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210742
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20651301
1313753	Tbk1	TANK-binding kinase 1	gene	MP:0031704	decreased interferon type I secretion		IEA		N	RGD:5509061	20260402	MGI			
1313755	Ndufab1	NADH:ubiquinone oxidoreductase subunit AB1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1313755	Ndufab1	NADH:ubiquinone oxidoreductase subunit AB1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1313755	Ndufab1	NADH:ubiquinone oxidoreductase subunit AB1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1313755	Ndufab1	NADH:ubiquinone oxidoreductase subunit AB1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1313755	Ndufab1	NADH:ubiquinone oxidoreductase subunit AB1	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1313755	Ndufab1	NADH:ubiquinone oxidoreductase subunit AB1	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1313755	Ndufab1	NADH:ubiquinone oxidoreductase subunit AB1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1313755	Ndufab1	NADH:ubiquinone oxidoreductase subunit AB1	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20210617	MGI			PMID:30814308
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20210617	MGI			PMID:30814308
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20210617	MGI			PMID:30814308
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20210617	MGI			PMID:30814308
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20210617	MGI			PMID:30814308
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0011017	increased body surface temperature		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20210422	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0014782	increased liver enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0014783	decreased liver enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:33177714
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20210617	MGI			PMID:30814308
1313759	Usp20	ubiquitin specific peptidase 20	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210617	MGI			PMID:30814308
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20160512	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160512	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20160512	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20160512	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20160512	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20160512	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20160512	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20160512	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0014238	abnormal ribosome morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0014906	abnormal muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:25816300
1313762	Mrps34	mitochondrial ribosomal protein S34	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:25816300
1313764	Palmd	palmdelphin	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1313764	Palmd	palmdelphin	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1313764	Palmd	palmdelphin	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20220310	MGI			PMID:34636652
1313764	Palmd	palmdelphin	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1313765	Tmem123	transmembrane protein 123	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1313767	Taf11	TATA-box binding protein associated factor 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313771	Ctdsp1	CTD small phosphatase 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20220811	MGI			
1313771	Ctdsp1	CTD small phosphatase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1313771	Ctdsp1	CTD small phosphatase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20170105	MGI			
1313771	Ctdsp1	CTD small phosphatase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20170105	MGI			
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20241121	MGI			
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479632
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356513
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304340
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304340
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304340
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356513
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304340
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356513
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304340
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877435
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304340
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356513
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877435
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254625
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304340
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356513
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877435
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254625
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0003927	increased cellular glucose import		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254625
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356513
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254625
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254625
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356513
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356513
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0005285	decreased unsaturated fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479632
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254625
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304340
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356513
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877435
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230601	MGI			
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:17254625
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:16877435
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:17003453
1313773	Elovl4	ELOVL fatty acid elongase 4	gene	MP:0030950	abnormal synaptic vesicle exocytosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:29168048
1313774	Cox19	cytochrome c oxidase assembly protein 19	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1313774	Cox19	cytochrome c oxidase assembly protein 19	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20160421	MGI			
1313774	Cox19	cytochrome c oxidase assembly protein 19	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1313774	Cox19	cytochrome c oxidase assembly protein 19	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313774	Cox19	cytochrome c oxidase assembly protein 19	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20221215	MGI			
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20463296
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20463296
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20191128	MGI			
1313776	Ash2l	ASH2 like histone lysine methyltransferase complex subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313778	Rrp1b	ribosomal RNA processing 1B	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20191128	MGI			
1313780	Ddx27	DEAD box helicase 27	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313782	Il1f10	interleukin 1 family, member 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191114	MGI			PMID:29554104
1313792	Ormdl2	ORM1-like 2 (S. cerevisiae)	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1313792	Ormdl2	ORM1-like 2 (S. cerevisiae)	gene	MP:0002531	abnormal type I hypersensitivity reaction		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1313792	Ormdl2	ORM1-like 2 (S. cerevisiae)	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1313792	Ormdl2	ORM1-like 2 (S. cerevisiae)	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1313792	Ormdl2	ORM1-like 2 (S. cerevisiae)	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1313792	Ormdl2	ORM1-like 2 (S. cerevisiae)	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1313792	Ormdl2	ORM1-like 2 (S. cerevisiae)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:37316542
1313792	Ormdl2	ORM1-like 2 (S. cerevisiae)	gene	MP:0020116	increased sphingosine level		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1313792	Ormdl2	ORM1-like 2 (S. cerevisiae)	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1313795	Ube2e2	ubiquitin-conjugating enzyme E2E 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20210128	MGI			
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170323	MGI			
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20211021	MGI			
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20191003	MGI			PMID:30745428
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20200402	MGI			
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0012206	increased neuronal stem cell self-renewal		IAGP		N	RGD:5509061	20191003	MGI			PMID:30745428
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0012306	enhanced spatial learning		IAGP		N	RGD:5509061	20191003	MGI			PMID:30745428
1313796	Ecrg4	ECRG4 augurin precursor	gene	MP:0012361	decreased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1313798	Chit1	chitinase 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826322
1313801	Fbxo7	F-box protein 7	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1313801	Fbxo7	F-box protein 7	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21652635
1313801	Fbxo7	F-box protein 7	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21652635
1313801	Fbxo7	F-box protein 7	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20141003	MGI			
1313801	Fbxo7	F-box protein 7	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20150430	MGI			
1313801	Fbxo7	F-box protein 7	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1313801	Fbxo7	F-box protein 7	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21652635
1313801	Fbxo7	F-box protein 7	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0008945	hyperchromic macrocytic anemia		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0010035	increased erythrocyte clearance		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1313801	Fbxo7	F-box protein 7	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21652635
1313801	Fbxo7	F-box protein 7	gene	MP:0011913	abnormal reticulocyte cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0013762	abnormal effector T cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313801	Fbxo7	F-box protein 7	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20190418	MGI			PMID:30840666
1313802	Xkr8	XK related 8	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0006428	ectopic Sertoli cells		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0009851	abnormal Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313802	Xkr8	XK related 8	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:31712393
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20015870
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0003926	decreased cellular glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313804	Mgat4a	mannoside acetylglucosaminyltransferase 4, isoenzyme A	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377570
1313805	Ccnq	cyclin Q	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1313805	Ccnq	cyclin Q	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1313805	Ccnq	cyclin Q	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1313805	Ccnq	cyclin Q	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313805	Ccnq	cyclin Q	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313805	Ccnq	cyclin Q	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1313807	Mkx	mohawk homeobox	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498044
1313807	Mkx	mohawk homeobox	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696843
1313807	Mkx	mohawk homeobox	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21254332
1313807	Mkx	mohawk homeobox	gene	MP:0013179	wavy tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696843
1313807	Mkx	mohawk homeobox	gene	MP:0030799	abnormal tendon sheath morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:20696843
1313808	Pear1	platelet endothelial aggregation receptor 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20201022	MGI			
1313808	Pear1	platelet endothelial aggregation receptor 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1313808	Pear1	platelet endothelial aggregation receptor 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20170202	MGI			PMID:27614188
1313811	Actl7b	actin-like 7b	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1313811	Actl7b	actin-like 7b	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313811	Actl7b	actin-like 7b	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36617158
1313815	Ppp2r5e	protein phosphatase 2, regulatory subunit B', epsilon	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1313815	Ppp2r5e	protein phosphatase 2, regulatory subunit B', epsilon	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1313815	Ppp2r5e	protein phosphatase 2, regulatory subunit B', epsilon	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1313815	Ppp2r5e	protein phosphatase 2, regulatory subunit B', epsilon	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1313815	Ppp2r5e	protein phosphatase 2, regulatory subunit B', epsilon	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1313815	Ppp2r5e	protein phosphatase 2, regulatory subunit B', epsilon	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1313817	Taf1c	TATA-box binding protein associated factor, RNA polymerase I, C	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1313817	Taf1c	TATA-box binding protein associated factor, RNA polymerase I, C	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1313817	Taf1c	TATA-box binding protein associated factor, RNA polymerase I, C	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1313817	Taf1c	TATA-box binding protein associated factor, RNA polymerase I, C	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1313817	Taf1c	TATA-box binding protein associated factor, RNA polymerase I, C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349843
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20181206	MGI			PMID:29584722
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20181206	MGI			PMID:29584722
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349843
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349843
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0003292	melena		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20181206	MGI			PMID:29584722
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349843
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0004963	abnormal blastocoele morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349843
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20180531	MGI			PMID:28533230
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20180531	MGI			PMID:28533230
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349843
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005567	decreased circulating total protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20180531	MGI			PMID:28533230
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0006064	abnormal superior vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0008109	abnormal small intestinal microvillus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0008141	decreased small intestinal microvillus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:28533230
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20180531	MGI			PMID:28533230
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20180531	MGI			PMID:28533230
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0008727	increased heart right atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0008732	reduced hair shaft melanin granule number		IAGP		N	RGD:5509061	20181227	MGI			PMID:29584722
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0009641	kidney degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0009979	abnormal cerebellum deep nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0010493	abnormal atrium myocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349843
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349843
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0011748	intestinal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0012028	abnormal visceral endoderm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322734
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0014226	abnormal alveolar macrophage physiology		IAGP		N	RGD:5509061	20180531	MGI			PMID:28533230
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0014229	decreased alveolar macrophage number		IAGP		N	RGD:5509061	20180531	MGI			PMID:28533230
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:21349843
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0030022	decreased muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:23673157
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0030914	abnormal endosome to melanosome transport		IAGP		N	RGD:5509061	20181227	MGI			PMID:29584722
1313819	Pikfyve	phosphoinositide kinase, FYVE type zinc finger containing	gene	MP:0030915	abnormal melanosome maturation		IAGP		N	RGD:5509061	20181227	MGI			PMID:29584722
1313823	Fbxw5	F-box and WD-40 domain protein 5	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20210114	MGI			PMID:32971071
1313823	Fbxw5	F-box and WD-40 domain protein 5	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20210114	MGI			PMID:32971071
1313823	Fbxw5	F-box and WD-40 domain protein 5	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20210114	MGI			PMID:32971071
1313823	Fbxw5	F-box and WD-40 domain protein 5	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20210114	MGI			PMID:32971071
1313823	Fbxw5	F-box and WD-40 domain protein 5	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20210114	MGI			PMID:32971071
1313823	Fbxw5	F-box and WD-40 domain protein 5	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240613	MGI			PMID:38697008
1313823	Fbxw5	F-box and WD-40 domain protein 5	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20210114	MGI			PMID:32971071
1313823	Fbxw5	F-box and WD-40 domain protein 5	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20210114	MGI			PMID:32971071
1313823	Fbxw5	F-box and WD-40 domain protein 5	gene	MP:0031217	increased susceptibility to myocardial ischemic injury		IAGP		N	RGD:5509061	20210114	MGI			PMID:32971071
1313825	Zfp143	zinc finger protein 143	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1313827	Rab40b	Rab40B, member RAS oncogene family	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20231207	MGI			
1313831	Unc45b	unc-45 myosin chaperone B	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1313831	Unc45b	unc-45 myosin chaperone B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313833	Vsx1	visual system homeobox 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20240523	MGI			
1313833	Vsx1	visual system homeobox 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15043821
1313833	Vsx1	visual system homeobox 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745032
1313833	Vsx1	visual system homeobox 1	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172916
1313833	Vsx1	visual system homeobox 1	gene	MP:0006075	abnormal retina cone bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745032
1313833	Vsx1	visual system homeobox 1	gene	MP:0006075	abnormal retina cone bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15043821
1313835	Paip1	polyadenylate binding protein-interacting protein 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1313835	Paip1	polyadenylate binding protein-interacting protein 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1313835	Paip1	polyadenylate binding protein-interacting protein 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230119	MGI			
1313835	Paip1	polyadenylate binding protein-interacting protein 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1313835	Paip1	polyadenylate binding protein-interacting protein 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230119	MGI			
1313835	Paip1	polyadenylate binding protein-interacting protein 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20230119	MGI			
1313835	Paip1	polyadenylate binding protein-interacting protein 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1313835	Paip1	polyadenylate binding protein-interacting protein 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230119	MGI			
1313836	Tmem132c	transmembrane protein 132C	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1313838	Lmo4	LIM domain only 4	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0000861	disorganized barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862160
1313838	Lmo4	LIM domain only 4	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691703
1313838	Lmo4	LIM domain only 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16949565
1313838	Lmo4	LIM domain only 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691703
1313838	Lmo4	LIM domain only 4	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16949565
1313838	Lmo4	LIM domain only 4	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16949565
1313838	Lmo4	LIM domain only 4	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16949565
1313838	Lmo4	LIM domain only 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691703
1313838	Lmo4	LIM domain only 4	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1313838	Lmo4	LIM domain only 4	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1313838	Lmo4	LIM domain only 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1313838	Lmo4	LIM domain only 4	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1313838	Lmo4	LIM domain only 4	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16949565
1313838	Lmo4	LIM domain only 4	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:16949565
1313838	Lmo4	LIM domain only 4	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20171019	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1313838	Lmo4	LIM domain only 4	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691703
1313838	Lmo4	LIM domain only 4	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0004568	fusion of glossopharyngeal and vagus nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691703
1313838	Lmo4	LIM domain only 4	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1313838	Lmo4	LIM domain only 4	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20618444
1313838	Lmo4	LIM domain only 4	gene	MP:0009594	abnormal corneocyte envelope morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16949565
1313838	Lmo4	LIM domain only 4	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:20618444
1313838	Lmo4	LIM domain only 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966286
1313838	Lmo4	LIM domain only 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913004
1313838	Lmo4	LIM domain only 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966285
1313838	Lmo4	LIM domain only 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691703
1313838	Lmo4	LIM domain only 4	gene	MP:0012686	everted embryonic neuroepithelium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691703
1313838	Lmo4	LIM domain only 4	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691703
1313838	Lmo4	LIM domain only 4	gene	MP:0012704	abnormal embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691703
1313839	Dip2b	disco interacting protein 2 homolog B	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1313839	Dip2b	disco interacting protein 2 homolog B	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:25138526
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20210819	MGI			PMID:25138526
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20210819	MGI			PMID:25138526
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:25138526
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23418755
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:25138526
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0005603	neuron hypertrophy		IAGP		N	RGD:5509061	20210819	MGI			PMID:25138526
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0008946	abnormal neuron number		IAGP		N	RGD:5509061	20210819	MGI			PMID:25138526
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0020067	increased neocortex size		IAGP		N	RGD:5509061	20210819	MGI			PMID:25138526
1313841	Spock3	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20210819	MGI			PMID:25138526
1313842	Prdm11	PR domain containing 11	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1313842	Prdm11	PR domain containing 11	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1313842	Prdm11	PR domain containing 11	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20191226	MGI			PMID:25499759
1313842	Prdm11	PR domain containing 11	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1313842	Prdm11	PR domain containing 11	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20191226	MGI			PMID:25499759
1313842	Prdm11	PR domain containing 11	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1313842	Prdm11	PR domain containing 11	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1313842	Prdm11	PR domain containing 11	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1313842	Prdm11	PR domain containing 11	gene	MP:0013707	abnormal hematopoietic precursor cell morphology		IAGP		N	RGD:5509061	20191226	MGI			PMID:23978475
1313842	Prdm11	PR domain containing 11	gene	MP:0020464	decreased megakaryocyte progenitor cell number		IAGP		N	RGD:5509061	20191226	MGI			PMID:23978475
1313842	Prdm11	PR domain containing 11	gene	MP:0020466	increased megakaryocyte progenitor cell proliferation		IAGP		N	RGD:5509061	20191226	MGI			PMID:23978475
1313846	Tmem126a	transmembrane protein 126A	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1313846	Tmem126a	transmembrane protein 126A	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1313846	Tmem126a	transmembrane protein 126A	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20200514	MGI			
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0000324	increased mast cell number		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20210114	MGI			PMID:32152231
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20210114	MGI			PMID:32152231
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0014264	abnormal perivascular vein cell coverage		IAGP		N	RGD:5509061	20230706	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0020326	dilated capillary		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0020327	abnormal capillary branching pattern		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313850	Adtrp	androgen dependent TFPI regulating protein	gene	MP:0020331	increased capillary tortuosity		IAGP		N	RGD:5509061	20201022	MGI			PMID:30571485
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20240523	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0001625	cardiac hypertrophy		IEA		N	RGD:5509061	20141003	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20141003	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230119	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20240523	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20141003	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20240523	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1313852	Bicral	BRD4 interacting chromatin remodeling complex associated protein like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1313856	Cmtm7	CKLF-like MARVEL transmembrane domain containing 7	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1313856	Cmtm7	CKLF-like MARVEL transmembrane domain containing 7	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1313856	Cmtm7	CKLF-like MARVEL transmembrane domain containing 7	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1313856	Cmtm7	CKLF-like MARVEL transmembrane domain containing 7	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1313856	Cmtm7	CKLF-like MARVEL transmembrane domain containing 7	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1313856	Cmtm7	CKLF-like MARVEL transmembrane domain containing 7	gene	MP:0008164	abnormal B-1a B cell morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1313856	Cmtm7	CKLF-like MARVEL transmembrane domain containing 7	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1313856	Cmtm7	CKLF-like MARVEL transmembrane domain containing 7	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1313856	Cmtm7	CKLF-like MARVEL transmembrane domain containing 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1313859	Pcmtd2	protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1313859	Pcmtd2	protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1313859	Pcmtd2	protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1313860	Naa25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210826	MGI			
1313860	Naa25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1313860	Naa25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1313860	Naa25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20220519	MGI			
1313860	Naa25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20221215	MGI			
1313860	Naa25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1313860	Naa25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1313860	Naa25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313860	Naa25	N(alpha)-acetyltransferase 25, NatB auxiliary subunit	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1313862	Rnasek	ribonuclease, RNase K	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1313862	Rnasek	ribonuclease, RNase K	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220519	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20170105	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0011483	renal glomerular synechia		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313864	Rhpn1	rhophilin, Rho GTPase binding protein 1	gene	MP:0011868	podocyte microvillus transformation		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1313866	Tmem254	transmembrane protein 254	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1313867	Slc25a42	solute carrier family 25, member 42	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1313867	Slc25a42	solute carrier family 25, member 42	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20220811	MGI			
1313867	Slc25a42	solute carrier family 25, member 42	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1313867	Slc25a42	solute carrier family 25, member 42	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313868	Il34	interleukin 34	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0005398	decreased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0008118	absent Langerhans cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0008119	decreased Langerhans cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0020943	increased susceptibility to Flaviviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:22729249
1313868	Il34	interleukin 34	gene	MP:0031044	increased susceptibility to Flaviviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:22729249
1313869	Sarnp	SAP domain containing ribonucleoprotein	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1313869	Sarnp	SAP domain containing ribonucleoprotein	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1313869	Sarnp	SAP domain containing ribonucleoprotein	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1313869	Sarnp	SAP domain containing ribonucleoprotein	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1313869	Sarnp	SAP domain containing ribonucleoprotein	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1313869	Sarnp	SAP domain containing ribonucleoprotein	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1313869	Sarnp	SAP domain containing ribonucleoprotein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1313869	Sarnp	SAP domain containing ribonucleoprotein	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20211021	MGI			
1313871	Abhd8	abhydrolase domain containing 8	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1313871	Abhd8	abhydrolase domain containing 8	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1313871	Abhd8	abhydrolase domain containing 8	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20170105	MGI			
1313871	Abhd8	abhydrolase domain containing 8	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1313871	Abhd8	abhydrolase domain containing 8	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1313871	Abhd8	abhydrolase domain containing 8	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1313871	Abhd8	abhydrolase domain containing 8	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1313875	Lsm14a	LSM14A mRNA processing body assembly factor	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1313875	Lsm14a	LSM14A mRNA processing body assembly factor	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1313875	Lsm14a	LSM14A mRNA processing body assembly factor	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1313875	Lsm14a	LSM14A mRNA processing body assembly factor	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1313875	Lsm14a	LSM14A mRNA processing body assembly factor	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1313877	Hsh2d	hematopoietic SH2 domain containing	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880512
1313877	Hsh2d	hematopoietic SH2 domain containing	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880512
1313877	Hsh2d	hematopoietic SH2 domain containing	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880512
1313877	Hsh2d	hematopoietic SH2 domain containing	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880512
1313877	Hsh2d	hematopoietic SH2 domain containing	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880512
1313880	Taf1a	TATA-box binding protein associated factor, RNA polymerase I, A	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1313880	Taf1a	TATA-box binding protein associated factor, RNA polymerase I, A	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1313880	Taf1a	TATA-box binding protein associated factor, RNA polymerase I, A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1313880	Taf1a	TATA-box binding protein associated factor, RNA polymerase I, A	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20241010	MGI			
1313882	P3h3	prolyl 3-hydroxylase 3	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1313882	P3h3	prolyl 3-hydroxylase 3	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1313882	P3h3	prolyl 3-hydroxylase 3	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20170810	MGI			PMID:28115524
1313882	P3h3	prolyl 3-hydroxylase 3	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:28115524
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20210520	MGI			
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0000642	enlarged adrenal glands		IEA		N	RGD:5509061	20210520	MGI			
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344468
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344468
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0003666	impaired sperm capacitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1313884	Catsper3	cation channel, sperm associated 3	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130785
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130785
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614141
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130785
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417741
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614141
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765423
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614141
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417741
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0010395	abnormal pharyngeal arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0012531	delayed limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0012720	elongated neck		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:19000668
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:12130785
1313886	Mbd4	methyl-CpG binding domain protein 4	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:19000668
1313888	Tbx5	T-box 5	gene	MP:0000158	absent sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736217
1313888	Tbx5	T-box 5	gene	MP:0000158	absent sternum		IAGP		N	RGD:5509061	20150903	MGI			PMID:25468972
1313888	Tbx5	T-box 5	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380715
1313888	Tbx5	T-box 5	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380715
1313888	Tbx5	T-box 5	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380715
1313888	Tbx5	T-box 5	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152185
1313888	Tbx5	T-box 5	gene	MP:0000551	absent forelimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736217
1313888	Tbx5	T-box 5	gene	MP:0000551	absent forelimb		IAGP		N	RGD:5509061	20150903	MGI			PMID:25468972
1313888	Tbx5	T-box 5	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:22728936
1313888	Tbx5	T-box 5	gene	MP:0001657	abnormal induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22728936
1313888	Tbx5	T-box 5	gene	MP:0001677	absent apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736217
1313888	Tbx5	T-box 5	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736217
1313888	Tbx5	T-box 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22728936
1313888	Tbx5	T-box 5	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380715
1313888	Tbx5	T-box 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380715
1313888	Tbx5	T-box 5	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289437
1313888	Tbx5	T-box 5	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22728936
1313888	Tbx5	T-box 5	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:25468972
1313888	Tbx5	T-box 5	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0004055	heart atrium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0004116	abnormal atrioventricular bundle conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22728936
1313888	Tbx5	T-box 5	gene	MP:0004117	abnormal atrioventricular bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289437
1313888	Tbx5	T-box 5	gene	MP:0004122	abnormal sinus arrhythmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0004123	abnormal impulse conducting system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289437
1313888	Tbx5	T-box 5	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0004339	absent clavicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736217
1313888	Tbx5	T-box 5	gene	MP:0004341	absent scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736217
1313888	Tbx5	T-box 5	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736217
1313888	Tbx5	T-box 5	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:25468972
1313888	Tbx5	T-box 5	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152185
1313888	Tbx5	T-box 5	gene	MP:0006141	abnormal atrioventricular node conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289437
1313888	Tbx5	T-box 5	gene	MP:0006142	abnormal sinoatrial node conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152185
1313888	Tbx5	T-box 5	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22728936
1313888	Tbx5	T-box 5	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:22728936
1313888	Tbx5	T-box 5	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289437
1313888	Tbx5	T-box 5	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380715
1313888	Tbx5	T-box 5	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380715
1313888	Tbx5	T-box 5	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380715
1313888	Tbx5	T-box 5	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0010520	sinoatrial block		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0010566	abnormal left posterior bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289437
1313888	Tbx5	T-box 5	gene	MP:0010567	abnormal right bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289437
1313888	Tbx5	T-box 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380715
1313888	Tbx5	T-box 5	gene	MP:0011953	prolonged PQ interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289437
1313888	Tbx5	T-box 5	gene	MP:0011953	prolonged PQ interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870172
1313888	Tbx5	T-box 5	gene	MP:0013164	abnormal forelimb bud morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:12736217
1313888	Tbx5	T-box 5	gene	MP:0013165	absent forelimb buds		IAGP		N	RGD:5509061	20150528	MGI			PMID:12736217
1313888	Tbx5	T-box 5	gene	MP:0031530	abnormal heart ventricle shape		IAGP		N	RGD:5509061	20240104	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0031711	monomorphic ventricular tachycardia		IAGP		N	RGD:5509061	20260528	MGI			PMID:22728936
1313888	Tbx5	T-box 5	gene	MP:0031757	second degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:11572777
1313888	Tbx5	T-box 5	gene	MP:0031757	second degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:22728936
1313888	Tbx5	T-box 5	gene	MP:0031761	Mobitz II atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:22728936
1313891	Larp4	La ribonucleoprotein 4	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20230831	MGI			PMID:28895529
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615442
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731460
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615442
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20171012	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615442
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24457099
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816794
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364326
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364326
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17980036
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521907
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17980036
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521907
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000906	abnormal trigeminal V mesencephalic nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000906	abnormal trigeminal V mesencephalic nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201224
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17980036
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816794
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731460
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615442
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001063	abnormal trochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001063	abnormal trochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731460
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001329	retina hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615442
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001684	abnormal axial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23811236
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23811236
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521907
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915318
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615442
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11291865
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002243	abnormal vomeronasal organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002698	abnormal sclera morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23811236
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764108
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003006	abnormal hippocampal fornix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731460
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201223
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615442
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764108
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364326
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17980036
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731460
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615442
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003877	abnormal serotonergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764108
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004096	abnormal midbrain-hindbrain boundary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731460
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004162	abnormal mammillary body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24457099
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816794
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004280	abnormal oculomotor nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004450	presphenoid bone hypoplasia		IAGP		N	RGD:5509061	20171207	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004457	abnormal orbitosphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23811236
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12652306
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0004990	abnormal ciliary ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10985852
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11291865
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16256739
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005247	abnormal extraocular muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005261	aniridia		IAGP		N	RGD:5509061	20160310	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005315	absent pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005549	retina pigment epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006100	abnormal tegmentum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12652306
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006100	abnormal tegmentum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006101	absent tegmentum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816794
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006105	small tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12652306
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006106	absent tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816794
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449667
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006149	decreased visual acuity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731460
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008262	abnormal hippocampus region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008325	abnormal gonadotroph morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23811236
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008335	decreased gonadotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23811236
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008914	enlarged cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008914	enlarged cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364326
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20161103	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20161103	MGI			PMID:15917450
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009038	decreased inferior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009048	enlarged tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009324	absent hippocampal fimbria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009578	otocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10985852
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731460
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615442
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009637	abnormal pretectal region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009637	abnormal pretectal region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21057506
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0010893	abnormal posterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0010893	abnormal posterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731460
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17980036
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12652306
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521907
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23811236
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21057506
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012083	absent foregut		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201223
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201224
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816794
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449667
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012090	midbrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234651
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12652306
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816794
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16845372
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201223
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449667
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532921
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7588062
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012170	absent optic placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012247	absent cornea		IAGP		N	RGD:5509061	20160310	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012267	abnormal red nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012276	absent prechordal mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012516	absent metencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012516	absent metencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201223
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201224
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:20816794
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012525	abnormal rhombic lip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11291865
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0012786	increased rhombomere 1 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0013595	absent vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0013906	absent embryonic telencephalon		IAGP		N	RGD:5509061	20150924	MGI			PMID:11731459
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0013906	absent embryonic telencephalon		IAGP		N	RGD:5509061	20150924	MGI			PMID:11820816
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0014061	ethmocephaly		IAGP		N	RGD:5509061	20230810	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0020515	abnormal visceral yolk sac endoderm morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0020516	abnormal visceral yolk sac mesenchyme morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:8565836
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0020534	increased pons size		IAGP		N	RGD:5509061	20180301	MGI			PMID:20816794
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0020534	increased pons size		IAGP		N	RGD:5509061	20180301	MGI			PMID:9895322
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0020543	decreased substantia nigra size		IAGP		N	RGD:5509061	20180301	MGI			PMID:9077465
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0030102	absent orbitosphenoid bone		IAGP		N	RGD:5509061	20170928	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0030320	abnormal temporal bone tympanic part morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0030324	abnormal anterior head development		IAGP		N	RGD:5509061	20171109	MGI			PMID:9811592
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0030324	abnormal anterior head development		IAGP		N	RGD:5509061	20180118	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0030558	absent nasopharynx		IAGP		N	RGD:5509061	20191219	MGI			PMID:7590242
1313893	Otx2	orthodenticle homeobox 2	gene	MP:0031442	enlarged cerebral aqueduct		IAGP		N	RGD:5509061	20221103	MGI			PMID:9077465
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685642
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685642
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685642
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10666340
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12930723
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15685642
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20231207	MGI			PMID:37062716
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:15685642
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20191017	MGI			PMID:15685642
1313895	H1f1	H1.1 linker histone, cluster member	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20200227	MGI			PMID:15685642
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313897	Caprin1	cell cycle associated protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861386
1313899	D7Ertd443e	DNA segment, Chr 7, ERATO Doi 443, expressed	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1313899	D7Ertd443e	DNA segment, Chr 7, ERATO Doi 443, expressed	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1313899	D7Ertd443e	DNA segment, Chr 7, ERATO Doi 443, expressed	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1313901	Armh3	armadillo-like helical domain containing 3	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313901	Armh3	armadillo-like helical domain containing 3	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313901	Armh3	armadillo-like helical domain containing 3	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160114	MGI			
1313901	Armh3	armadillo-like helical domain containing 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1313903	Ap1g2	adaptor protein complex AP-1, gamma 2 subunit	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1313903	Ap1g2	adaptor protein complex AP-1, gamma 2 subunit	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
1313905	Foxn3	forkhead box N3	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1313905	Foxn3	forkhead box N3	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0009891	abnormal palate bone morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313905	Foxn3	forkhead box N3	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0030082	long lower incisors		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0030083	long upper incisors		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0030279	thin neurocranium		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313905	Foxn3	forkhead box N3	gene	MP:0030320	abnormal temporal bone tympanic part morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:20691664
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20181227	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20170105	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1313911	Zswim1	zinc finger SWIM-type containing 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1313913	Hat1	histone aminotransferase 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0005649	increased spleen neoplasm incidence		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0010294	increased kidney tumor incidence		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754951
1313913	Hat1	histone aminotransferase 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313913	Hat1	histone aminotransferase 1	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20220929	MGI			PMID:31290578
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29247201
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20181220	MGI			PMID:29848638
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20181220	MGI			PMID:29848638
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29247201
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20190502	MGI			
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20180222	MGI			PMID:29247201
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20181220	MGI			PMID:29848638
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20211021	MGI			
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20181220	MGI			PMID:29848638
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20180222	MGI			PMID:29247201
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:29247201
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29247201
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20181220	MGI			PMID:29848638
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:29247201
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313914	Sox30	SRY (sex determining region Y)-box 30	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20220721	MGI			PMID:29866902
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940080
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940080
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940080
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940080
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940080
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20160609	MGI			PMID:26511242
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0011621	abnormal habituation to a novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940080
1313916	Nat8l	N-acetyltransferase 8-like	gene	MP:0014365	impaired short-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:33638175
1313921	Tmem14c	transmembrane protein 14C	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:25157825
1313921	Tmem14c	transmembrane protein 14C	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:25157825
1313921	Tmem14c	transmembrane protein 14C	gene	MP:0001588	abnormal hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:25157825
1313921	Tmem14c	transmembrane protein 14C	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:25157825
1313921	Tmem14c	transmembrane protein 14C	gene	MP:0008956	decreased cellular hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:25157825
1313921	Tmem14c	transmembrane protein 14C	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:25157825
1313921	Tmem14c	transmembrane protein 14C	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:25157825
1313921	Tmem14c	transmembrane protein 14C	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:25157825
1313921	Tmem14c	transmembrane protein 14C	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:25157825
1313924	Fbxl4	F-box and leucine-rich repeat protein 4	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20210415	MGI			PMID:32525278
1313924	Fbxl4	F-box and leucine-rich repeat protein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210415	MGI			PMID:32525278
1313924	Fbxl4	F-box and leucine-rich repeat protein 4	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32525278
1313924	Fbxl4	F-box and leucine-rich repeat protein 4	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20210415	MGI			PMID:32525278
1313924	Fbxl4	F-box and leucine-rich repeat protein 4	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20210415	MGI			PMID:32525278
1313924	Fbxl4	F-box and leucine-rich repeat protein 4	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32525278
1313924	Fbxl4	F-box and leucine-rich repeat protein 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210415	MGI			PMID:32525278
1313924	Fbxl4	F-box and leucine-rich repeat protein 4	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20210415	MGI			PMID:32525278
1313924	Fbxl4	F-box and leucine-rich repeat protein 4	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20210415	MGI			PMID:32525278
1313926	Vstm2l	V-set and transmembrane domain containing 2-like	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1313926	Vstm2l	V-set and transmembrane domain containing 2-like	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1313926	Vstm2l	V-set and transmembrane domain containing 2-like	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1313931	Mknk2	MAP kinase-interacting serine/threonine kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254222
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174920
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17330141
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17330141
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17494763
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17494763
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17494763
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20260813	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174920
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102539
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102539
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102539
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102539
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174920
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17494763
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17494763
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174920
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17330141
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20180301	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695510
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10380922
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:16481437
1313933	Lrp8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	gene	MP:0030956	abnormal neuronal precursor cell migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:17494763
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798193
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798193
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798193
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798193
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20240118	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16317048
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0003085	abnormal egg cylinder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798193
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0010496	abnormal pectinate muscle morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976450
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798193
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0011198	absent proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798193
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0020135	abnormal heart ventricle wall thickness		IAGP		N	RGD:5509061	20240118	MGI			PMID:19652092
1313938	Lims1	LIM and senescent cell antigen-like domains 1	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231102	MGI			PMID:19652092
1313939	Bmerb1	bMERB domain containing 1	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20200402	MGI			
1313939	Bmerb1	bMERB domain containing 1	gene	MP:0000613	abnormal salivary gland morphology		IEA		N	RGD:5509061	20200402	MGI			
1313939	Bmerb1	bMERB domain containing 1	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20200402	MGI			
1313939	Bmerb1	bMERB domain containing 1	gene	MP:0000642	enlarged adrenal glands		IEA		N	RGD:5509061	20200402	MGI			
1313941	Ilf2	interleukin enhancer binding factor 2	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20051514
1313945	Prxl2c	peroxiredoxin like 2C	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1313945	Prxl2c	peroxiredoxin like 2C	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1313947	Upf1	UPF1 RNA helicase and ATPase	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11152657
1313947	Upf1	UPF1 RNA helicase and ATPase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11152657
1313947	Upf1	UPF1 RNA helicase and ATPase	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11152657
1313947	Upf1	UPF1 RNA helicase and ATPase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11152657
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20150205	MGI			PMID:24715463
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20160421	MGI			
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150205	MGI			PMID:24715463
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1313950	Adam23	a disintegrin and metallopeptidase domain 23	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313952	Cybrd1	cytochrome b reductase 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1313952	Cybrd1	cytochrome b reductase 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15961514
1313952	Cybrd1	cytochrome b reductase 1	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15961514
1313956	Tia1	cytotoxic granule-associated RNA binding protein 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769925
1313956	Tia1	cytotoxic granule-associated RNA binding protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769925
1313956	Tia1	cytotoxic granule-associated RNA binding protein 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921895
1313956	Tia1	cytotoxic granule-associated RNA binding protein 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769925
1313956	Tia1	cytotoxic granule-associated RNA binding protein 1	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769925
1313956	Tia1	cytotoxic granule-associated RNA binding protein 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921895
1313956	Tia1	cytotoxic granule-associated RNA binding protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921895
1313956	Tia1	cytotoxic granule-associated RNA binding protein 1	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:14769925
1313959	Drc5	dynein regulatory complex subunit 5	gene	MP:0001124	abnormal gametes		IAGP		N	RGD:5509061	20180208	MGI			PMID:28630322
1313959	Drc5	dynein regulatory complex subunit 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20180208	MGI			PMID:28630322
1313959	Drc5	dynein regulatory complex subunit 5	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20180208	MGI			PMID:28630322
1313959	Drc5	dynein regulatory complex subunit 5	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20180208	MGI			PMID:28630322
1313961	Stac	src homology three (SH3) and cysteine rich domain	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20220519	MGI			
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15041039
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20210520	MGI			
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15041039
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12709397
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:24285835
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0002425	abnormal susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:10553062
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200068
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15041039
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700209
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10553062
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721841
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10553062
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15041039
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721841
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10553062
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700209
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15041039
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700209
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700209
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119024
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721841
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10553062
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24285835
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700209
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370359
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15041039
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24285835
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008600	decreased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15041039
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24285835
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721841
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721841
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24285835
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370359
1313965	Stat4	signal transducer and activator of transcription 4	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700209
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926768
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926768
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080592
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926768
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080592
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20111116	MGI			
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926768
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926768
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926768
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0003460	decreased fear-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15777636
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926768
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0005198	abnormal aqueous drainage system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0005203	abnormal trabecular meshwork morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0005204	abnormal canal of Schlemm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15777636
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0008161	increased diameter of radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0008163	increased diameter of ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080592
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0009039	absent inferior colliculus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0009877	exostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0009894	absent hard palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:28445472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0010079	increased osteochondroma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0010079	increased osteochondroma incidence		IAGP		N	RGD:5509061	20171228	MGI			PMID:20080592
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0010079	increased osteochondroma incidence		IAGP		N	RGD:5509061	20171228	MGI			PMID:28445472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0010714	iris coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0010719	ciliary body coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14605369
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926768
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080592
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080592
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080592
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:22411800
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0030443	abnormal cranial synchondrosis		IAGP		N	RGD:5509061	20171228	MGI			PMID:28445472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0030883	dislocated radius head		IAGP		N	RGD:5509061	20181101	MGI			PMID:20534475
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:19509472
1313967	Ext1	exostosin glycosyltransferase 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22411800
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:791749
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:791749
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0000416	sparse hair		IEA		N	RGD:5509061	20111116	MGI			
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:791749
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0000427	abnormal hair cycle		IEA		N	RGD:5509061	20111116	MGI			
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:791749
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:791749
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0002991	abnormal sebaceous gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0003846	matted coat		IEA		N	RGD:5509061	20111116	MGI			
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0005114	premature hair loss		IEA		N	RGD:5509061	20111116	MGI			
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0008731	abnormal hair shaft melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:791749
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0008767	abnormal hair medullary septa cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:791749
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0009794	sebaceous gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0010683	dilated hair follicle infundibulum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0011194	abnormal hair follicle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956733
1313970	Zdhhc21	zinc finger, DHHC domain containing 21	gene	MP:0013373	increased sebum secretion		IAGP		N	RGD:5509061	20141218	MGI			PMID:19956733
1313973	Psmd2	proteasome (prosome, macropain) 26S subunit, non-ATPase, 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1313973	Psmd2	proteasome (prosome, macropain) 26S subunit, non-ATPase, 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1313980	Tymp	thymidine phosphorylase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077348
1313980	Tymp	thymidine phosphorylase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077348
1313980	Tymp	thymidine phosphorylase	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077348
1313980	Tymp	thymidine phosphorylase	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077348
1313980	Tymp	thymidine phosphorylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20251030	MGI			PMID:12077348
1313980	Tymp	thymidine phosphorylase	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0009980	abnormal cerebellum dentate nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0014958	decreased lung enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0014966	decreased heart enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:12077348
1313980	Tymp	thymidine phosphorylase	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0014970	decreased muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0014972	decreased spleen enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313980	Tymp	thymidine phosphorylase	gene	MP:0014975	decreased kidney enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19028666
1313983	Clmp	CXADR-like membrane protein	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20170323	MGI			
1313983	Clmp	CXADR-like membrane protein	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20180726	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0003589	abnormal ureter physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0004142	abnormal muscle tone		IAGP		N	RGD:5509061	20180726	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20170323	MGI			
1313983	Clmp	CXADR-like membrane protein	gene	MP:0006144	increased systemic arterial systolic blood pressure		IEA		N	RGD:5509061	20170323	MGI			
1313983	Clmp	CXADR-like membrane protein	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0009480	distended cecum		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0009642	abnormal blood homeostasis		IEA		N	RGD:5509061	20170323	MGI			
1313983	Clmp	CXADR-like membrane protein	gene	MP:0009854	impaired gastric peristalsis		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0011082	abnormal gastrointestinal motility		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180726	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20200310	MGI			
1313983	Clmp	CXADR-like membrane protein	gene	MP:0011426	abnormal ureter smooth muscle morphology		IAGP		N	RGD:5509061	20180726	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0011480	impaired ureteric peristalsis		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0013862	abnormal cecum position		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0013954	increased intestine length		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0014022	abnormal duodenum topology		IAGP		N	RGD:5509061	20180719	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0014023	abnormal intestine placement		IAGP		N	RGD:5509061	20180726	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0014279	abnormal intestinal rotation		IAGP		N	RGD:5509061	20230810	MGI			PMID:29361518
1313983	Clmp	CXADR-like membrane protein	gene	MP:0020989	increased urine lipocalin 2 level		IAGP		N	RGD:5509061	20211216	MGI			PMID:29361518
1313985	Pxn	paxillin	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313985	Pxn	paxillin	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313985	Pxn	paxillin	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313985	Pxn	paxillin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313985	Pxn	paxillin	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313985	Pxn	paxillin	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313985	Pxn	paxillin	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313985	Pxn	paxillin	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313985	Pxn	paxillin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313985	Pxn	paxillin	gene	MP:0012499	absent cardiogenic plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784865
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127714
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127714
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675084
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127714
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509261
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141330
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0001999	photosensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675084
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11454706
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141330
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141330
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509261
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141330
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15533840
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11454706
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509261
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675084
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675084
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16141330
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12555660
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15533840
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841728
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393014
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1313987	Xpc	xeroderma pigmentosum, complementation group C	gene	MP:0014762	impaired base-excision repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:17326724
1313989	Mylip	myosin regulatory light chain interacting protein	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1313989	Mylip	myosin regulatory light chain interacting protein	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1313989	Mylip	myosin regulatory light chain interacting protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
1313989	Mylip	myosin regulatory light chain interacting protein	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230119	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230119	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0012111	failure of morula compaction		IEA		N	RGD:5509061	20241010	MGI			
1313991	Ebna1bp2	EBNA1 binding protein 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1313994	Nusap1	nucleolar and spindle associated protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20807801
1313994	Nusap1	nucleolar and spindle associated protein 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20807801
1313994	Nusap1	nucleolar and spindle associated protein 1	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20807801
1313994	Nusap1	nucleolar and spindle associated protein 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:20807801
1313994	Nusap1	nucleolar and spindle associated protein 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20807801
1313994	Nusap1	nucleolar and spindle associated protein 1	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:20807801
1313994	Nusap1	nucleolar and spindle associated protein 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20807801
1313994	Nusap1	nucleolar and spindle associated protein 1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20807801
1313994	Nusap1	nucleolar and spindle associated protein 1	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20807801
1313999	Cpsf3	cleavage and polyadenylation specificity factor 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313999	Cpsf3	cleavage and polyadenylation specificity factor 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1313999	Cpsf3	cleavage and polyadenylation specificity factor 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1313999	Cpsf3	cleavage and polyadenylation specificity factor 3	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18560593
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492057
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265660
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492057
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265660
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17563363
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:17563363
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265660
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265660
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180215	MGI			PMID:28360124
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265660
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285945
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18560593
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421046
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28360124
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17563363
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21385841
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421046
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0003908	decreased stereotypic behavior		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285945
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421046
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18560593
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21385841
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28360124
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17563363
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492057
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21249202
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21385841
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265660
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492057
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21249202
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21385841
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20141127	MGI			PMID:25296918
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21249202
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21249202
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21249202
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0008830	abnormal nucleolus morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28360124
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421046
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22265660
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285945
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492057
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492057
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285945
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492057
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0011975	neuronal cytoplasmic inclusions		IAGP		N	RGD:5509061	20150402	MGI			PMID:25609609
1314002	Pink1	PTEN induced putative kinase 1	gene	MP:0014910	decreased hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:19492057
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0003049	abnormal lumbar vertebrae morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0003050	abnormal sacral vertebrae morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0003271	abnormal duodenum morphology		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210826	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1314004	Rbm22	RNA binding motif protein 22	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1314006	Casp8ap2	caspase 8 associated protein 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725362
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795391
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795391
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:19154719
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795391
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0000963	fused dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795391
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795391
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19154719
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19154719
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0004612	fusion of vertebral bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795391
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998026
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19154719
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21498671
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0012670	prolonged somite segmentation clock period		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795391
1314007	Nrarp	Notch-regulated ankyrin repeat protein	gene	MP:0020316	decreased vascular endothelial cell proliferation		IAGP		N	RGD:5509061	20160616	MGI			PMID:19154719
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20191226	MGI			PMID:26987296
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220811	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20220811	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0006325	impaired hearing		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0011090	perinatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0013179	wavy tail		IEA		N	RGD:5509061	20141003	MGI			
1314008	Clec16a	C-type lectin domain family 16, member A	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20160519	MGI			PMID:24949970
1314014	Inpp5f	inositol polyphosphate-5-phosphatase F	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19875726
1314014	Inpp5f	inositol polyphosphate-5-phosphatase F	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19875726
1314014	Inpp5f	inositol polyphosphate-5-phosphatase F	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19875726
1314014	Inpp5f	inositol polyphosphate-5-phosphatase F	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19875726
1314018	Atmin	ATM interactor	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20150416	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20160414	MGI			PMID:26832406
1314018	Atmin	ATM interactor	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:24852369
1314018	Atmin	ATM interactor	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0003115	abnormal respiratory system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24852369
1314018	Atmin	ATM interactor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0004967	abnormal kidney epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24852369
1314018	Atmin	ATM interactor	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160414	MGI			PMID:26832406
1314018	Atmin	ATM interactor	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891272
1314018	Atmin	ATM interactor	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20160414	MGI			PMID:26832406
1314018	Atmin	ATM interactor	gene	MP:0008404	increased cellular sensitivity to methylmethanesulfonate induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160414	MGI			PMID:26832406
1314018	Atmin	ATM interactor	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20160414	MGI			PMID:26832406
1314018	Atmin	ATM interactor	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0009796	abnormal base-excision repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20160414	MGI			PMID:26832406
1314018	Atmin	ATM interactor	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20160414	MGI			PMID:26832406
1314018	Atmin	ATM interactor	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1314018	Atmin	ATM interactor	gene	MP:0010885	absent trachea		IAGP		N	RGD:5509061	20150212	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20889973
1314018	Atmin	ATM interactor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160414	MGI			PMID:26832406
1314018	Atmin	ATM interactor	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0013213	abnormal embryonic neuroepithelium primary cilium morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:25294941
1314018	Atmin	ATM interactor	gene	MP:0013496	abnormal trachea development		IAGP		N	RGD:5509061	20150212	MGI			PMID:20975950
1314018	Atmin	ATM interactor	gene	MP:0030169	thick upper lip		IAGP		N	RGD:5509061	20171005	MGI			PMID:25294941
1314020	Snx10	sorting nexin 10	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210826	MGI			
1314020	Snx10	sorting nexin 10	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0005190	osteomyelitis		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0010926	increased osteoid volume		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0012336	decreased vitamin D level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0012336	decreased vitamin D level		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0013639	decreased bone stiffness		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1314020	Snx10	sorting nexin 10	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0030505	tooth impaction		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314020	Snx10	sorting nexin 10	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20200730	MGI			PMID:32278070
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20250508	MGI			
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240613	MGI			PMID:33563757
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20260402	MGI			
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20240613	MGI			PMID:33563757
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20240613	MGI			PMID:33563757
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20240613	MGI			PMID:33563757
1314022	Hmgxb4	HMG box domain containing 4	gene	MP:0011077	decreased macrophage nitric oxide production		IAGP		N	RGD:5509061	20240613	MGI			PMID:33563757
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314024	Elmo2	engulfment and cell motility 2	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0000798	abnormal frontal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0009979	abnormal cerebellum deep nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16377659
1314026	Manba	mannosidase, beta A, lysosomal	gene	MP:0031148	abnormal liver sinusoidal endothelial cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:16377659
1314028	Plek2	pleckstrin 2	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210128	MGI			
1314028	Plek2	pleckstrin 2	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1314028	Plek2	pleckstrin 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0011913	abnormal reticulocyte cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1314028	Plek2	pleckstrin 2	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:29202466
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20171221	MGI			PMID:28578315
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20171221	MGI			PMID:28578315
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20171221	MGI			PMID:28578315
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28578315
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20171221	MGI			PMID:28578315
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20171221	MGI			PMID:28578315
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0008581	disorganized photoreceptor inner segment		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28578315
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160804	MGI			
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314030	Agpat3	1-acylglycerol-3-phosphate O-acyltransferase 3	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:28578316
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20241121	MGI			
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20200514	MGI			
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23207902
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23207902
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23207902
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23207902
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20200514	MGI			
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23207902
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23207902
1314032	Scmh1	Scm polycomb group homolog 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:17215307
1314034	Wdr1	WD repeat domain 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12955145
1314034	Wdr1	WD repeat domain 1	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151112	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20170803	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0003405	abnormal platelet shape		IAGP		N	RGD:5509061	20170803	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0004721	abnormal platelet dense granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0010570	prolonged ST segment		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151015	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314034	Wdr1	WD repeat domain 1	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1314034	Wdr1	WD repeat domain 1	gene	MP:0014060	abnormal platelet alpha-granule morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:17515402
1314034	Wdr1	WD repeat domain 1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:24840128
1314034	Wdr1	WD repeat domain 1	gene	MP:0031742	increased T wave amplitude		IAGP		N	RGD:5509061	20260716	MGI			PMID:24840128
1314038	Snx8	sorting nexin 8	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1314038	Snx8	sorting nexin 8	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1314038	Snx8	sorting nexin 8	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314038	Snx8	sorting nexin 8	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314038	Snx8	sorting nexin 8	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314038	Snx8	sorting nexin 8	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1314038	Snx8	sorting nexin 8	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1314038	Snx8	sorting nexin 8	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1314038	Snx8	sorting nexin 8	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1314038	Snx8	sorting nexin 8	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314038	Snx8	sorting nexin 8	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314038	Snx8	sorting nexin 8	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314038	Snx8	sorting nexin 8	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20181227	MGI			
1314038	Snx8	sorting nexin 8	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314038	Snx8	sorting nexin 8	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314038	Snx8	sorting nexin 8	gene	MP:0031219	decreased circulating CXCL10 level		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314038	Snx8	sorting nexin 8	gene	MP:0031222	decreased CXCL10 secretion		IAGP		N	RGD:5509061	20210708	MGI			PMID:29180417
1314040	Krt36	keratin 36	gene	MP:0000763	abnormal filiform papillae morphology		IEA		N	RGD:5509061	20170420	MGI			
1314040	Krt36	keratin 36	gene	MP:0001242	hyperkeratosis		IEA		N	RGD:5509061	20170420	MGI			
1314040	Krt36	keratin 36	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20170420	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210520	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200402	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210520	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210520	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20190502	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31845480
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20211021	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20200402	MGI			
1314042	Wbp1l	WW domain binding protein 1 like	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1314046	Trim21	tripartite motif-containing 21	gene	MP:0000622	increased salivation		IAGP		N	RGD:5509061	20240516	MGI			PMID:33957127
1314046	Trim21	tripartite motif-containing 21	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494276
1314046	Trim21	tripartite motif-containing 21	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314046	Trim21	tripartite motif-containing 21	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19635858
1314049	Ttc39b	tetratricopeptide repeat domain 39B	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1314049	Ttc39b	tetratricopeptide repeat domain 39B	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20160804	MGI			
1314049	Ttc39b	tetratricopeptide repeat domain 39B	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20160804	MGI			
1314051	Mboat2	membrane bound O-acyltransferase domain containing 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1314051	Mboat2	membrane bound O-acyltransferase domain containing 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1314051	Mboat2	membrane bound O-acyltransferase domain containing 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1314051	Mboat2	membrane bound O-acyltransferase domain containing 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1314051	Mboat2	membrane bound O-acyltransferase domain containing 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1314051	Mboat2	membrane bound O-acyltransferase domain containing 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1314051	Mboat2	membrane bound O-acyltransferase domain containing 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210520	MGI			
1314051	Mboat2	membrane bound O-acyltransferase domain containing 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20220811	MGI			
1314057	Hoxc9	homeobox C9	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547473
1314057	Hoxc9	homeobox C9	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314057	Hoxc9	homeobox C9	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314059	Snx15	sorting nexin 15	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1314059	Snx15	sorting nexin 15	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1314059	Snx15	sorting nexin 15	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201231	MGI			
1314059	Snx15	sorting nexin 15	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1314059	Snx15	sorting nexin 15	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220519	MGI			
1314059	Snx15	sorting nexin 15	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1314059	Snx15	sorting nexin 15	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1314061	Dusp2	dual specificity phosphatase 2	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16474395
1314061	Dusp2	dual specificity phosphatase 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16474395
1314061	Dusp2	dual specificity phosphatase 2	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16474395
1314061	Dusp2	dual specificity phosphatase 2	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16474395
1314065	Stra6l	STRA6-like	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1314065	Stra6l	STRA6-like	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20170105	MGI			
1314065	Stra6l	STRA6-like	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1314065	Stra6l	STRA6-like	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1314065	Stra6l	STRA6-like	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1314065	Stra6l	STRA6-like	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1314065	Stra6l	STRA6-like	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1314065	Stra6l	STRA6-like	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1314073	Osr2	odd-skipped related 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175245
1314073	Osr2	odd-skipped related 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389375
1314073	Osr2	odd-skipped related 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19341725
1314073	Osr2	odd-skipped related 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19631205
1314073	Osr2	odd-skipped related 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1314073	Osr2	odd-skipped related 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19631205
1314073	Osr2	odd-skipped related 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1314073	Osr2	odd-skipped related 2	gene	MP:0000128	growth retardation of molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:19631205
1314073	Osr2	odd-skipped related 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19341725
1314073	Osr2	odd-skipped related 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:19341725
1314073	Osr2	odd-skipped related 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389375
1314073	Osr2	odd-skipped related 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175245
1314073	Osr2	odd-skipped related 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389375
1314073	Osr2	odd-skipped related 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175245
1314073	Osr2	odd-skipped related 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19631205
1314073	Osr2	odd-skipped related 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17941042
1314073	Osr2	odd-skipped related 2	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262216
1314073	Osr2	odd-skipped related 2	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262216
1314073	Osr2	odd-skipped related 2	gene	MP:0003190	fused synovial joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262216
1314073	Osr2	odd-skipped related 2	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389375
1314073	Osr2	odd-skipped related 2	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1314073	Osr2	odd-skipped related 2	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19631205
1314073	Osr2	odd-skipped related 2	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389375
1314073	Osr2	odd-skipped related 2	gene	MP:0009263	abnormal eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389375
1314073	Osr2	odd-skipped related 2	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389375
1314073	Osr2	odd-skipped related 2	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262216
1314073	Osr2	odd-skipped related 2	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221027	MGI			PMID:34557486
1314073	Osr2	odd-skipped related 2	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34557486
1314073	Osr2	odd-skipped related 2	gene	MP:0009884	palatal shelf fusion with tongue or mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1314073	Osr2	odd-skipped related 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175245
1314073	Osr2	odd-skipped related 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1314073	Osr2	odd-skipped related 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175245
1314073	Osr2	odd-skipped related 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19631205
1314073	Osr2	odd-skipped related 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1314073	Osr2	odd-skipped related 2	gene	MP:0010864	abnormal enamel knot morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:19631205
1314073	Osr2	odd-skipped related 2	gene	MP:0011087	neonatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1314073	Osr2	odd-skipped related 2	gene	MP:0012163	abnormal dental mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19631205
1314073	Osr2	odd-skipped related 2	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20230302	MGI			PMID:19389375
1314073	Osr2	odd-skipped related 2	gene	MP:0021202	abnormal palatopharyngeus muscle morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34557486
1314073	Osr2	odd-skipped related 2	gene	MP:0021203	abnormal palatine aponeurosis morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34557486
1314073	Osr2	odd-skipped related 2	gene	MP:0021204	abnormal superior pharyngeal constrictor muscle morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34557486
1314073	Osr2	odd-skipped related 2	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:15175245
1314073	Osr2	odd-skipped related 2	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:19389375
1314073	Osr2	odd-skipped related 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:15175245
1314073	Osr2	odd-skipped related 2	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:21420399
1314073	Osr2	odd-skipped related 2	gene	MP:0030293	small tensor veli palatini muscle		IAGP		N	RGD:5509061	20221027	MGI			PMID:34557486
1314073	Osr2	odd-skipped related 2	gene	MP:0030295	small levator veli palatini muscle		IAGP		N	RGD:5509061	20221027	MGI			PMID:34557486
1314079	Kera	keratocan	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911102
1314079	Kera	keratocan	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911102
1314079	Kera	keratocan	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665512
1314079	Kera	keratocan	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20201231	MGI			
1314079	Kera	keratocan	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665512
1314079	Kera	keratocan	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911102
1314088	Cep20	centrosomal protein 20	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314088	Cep20	centrosomal protein 20	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20220505	MGI			PMID:33686659
1314091	Tpte	transmembrane phosphatase with tensin homology	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20230601	MGI			
1314091	Tpte	transmembrane phosphatase with tensin homology	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20201015	MGI			PMID:31776261
1314091	Tpte	transmembrane phosphatase with tensin homology	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1314091	Tpte	transmembrane phosphatase with tensin homology	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20201015	MGI			PMID:31776261
1314091	Tpte	transmembrane phosphatase with tensin homology	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20230601	MGI			
1314091	Tpte	transmembrane phosphatase with tensin homology	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31776261
1314091	Tpte	transmembrane phosphatase with tensin homology	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31776261
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20220324	MGI			PMID:35216179
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20220324	MGI			PMID:35216179
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20220324	MGI			PMID:35216179
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314093	Dnajb4	DnaJ heat shock protein family (Hsp40) member B4	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20230330	MGI			PMID:36512060
1314095	Cndp2	CNDP dipeptidase 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1314095	Cndp2	CNDP dipeptidase 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1314095	Cndp2	CNDP dipeptidase 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1314095	Cndp2	CNDP dipeptidase 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1314095	Cndp2	CNDP dipeptidase 2	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1314095	Cndp2	CNDP dipeptidase 2	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210128	MGI			
1314095	Cndp2	CNDP dipeptidase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1314095	Cndp2	CNDP dipeptidase 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1314095	Cndp2	CNDP dipeptidase 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000103	nasal bone hypoplasia		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20201022	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20230601	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0000614	absent salivary gland		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20200514	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001394	circling		IEA		N	RGD:5509061	20141003	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20141003	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230601	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20230601	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0004197	abnormal fetal growth/weight/body size		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0004352	absent humerus		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0004475	palatine bone hypoplasia		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0004870	small premaxilla		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20230601	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009893	cleft primary palate		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009893	cleft primary palate		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0013546	cleft soft palate		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:26371508
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230309	MGI			PMID:32253237
1314096	Esrp1	epithelial splicing regulatory protein 1	gene	MP:0031504	increased mouth width		IAGP		N	RGD:5509061	20230810	MGI			PMID:26371508
1314100	Calhm4	calcium homeostasis modulator family member 4	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1314100	Calhm4	calcium homeostasis modulator family member 4	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1314105	Zgrf1	zinc finger, GRF-type containing 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1314105	Zgrf1	zinc finger, GRF-type containing 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1314107	Tectb	tectorin beta	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220887
1314107	Tectb	tectorin beta	gene	MP:0004417	decreased cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220887
1314107	Tectb	tectorin beta	gene	MP:0004591	enlarged tectorial membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220887
1314107	Tectb	tectorin beta	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220887
1314107	Tectb	tectorin beta	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220887
1314107	Tectb	tectorin beta	gene	MP:0006384	enhanced cochlear frequency tuning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220887
1314107	Tectb	tectorin beta	gene	MP:0013962	absent Hensen stripe		IAGP		N	RGD:5509061	20160310	MGI			PMID:17220887
1314107	Tectb	tectorin beta	gene	MP:0014089	abnormal tectorial membrane marginal band morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:17220887
1314107	Tectb	tectorin beta	gene	MP:0014091	abnormal tectorial membrane striated-sheet matrix morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:17220887
1314109	Rasgef1a	RasGEF domain family, member 1A	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1314112	Dppa5a	developmental pluripotency associated 5A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16504174
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20181227	MGI			
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170504	MGI			
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20181227	MGI			
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314114	Arih2	ariadne RBR E3 ubiquitin protein ligase 2	gene	MP:0011625	cystolithiasis		IEA		N	RGD:5509061	20181227	MGI			
1314116	Abcg4	ATP binding cassette subfamily G member 4	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039927
1314116	Abcg4	ATP binding cassette subfamily G member 4	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039927
1314116	Abcg4	ATP binding cassette subfamily G member 4	gene	MP:0003193	decreased cholesterol efflux		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039927
1314116	Abcg4	ATP binding cassette subfamily G member 4	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039927
1314121	Caln1	calneuron 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20231019	MGI			PMID:37355986
1314121	Caln1	calneuron 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20231019	MGI			PMID:37355986
1314121	Caln1	calneuron 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20231019	MGI			PMID:37355986
1314121	Caln1	calneuron 1	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37355986
1314121	Caln1	calneuron 1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37355986
1314121	Caln1	calneuron 1	gene	MP:0011149	abnormal hippocampus stratum lacunosum morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37355986
1314121	Caln1	calneuron 1	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37355986
1314121	Caln1	calneuron 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20231019	MGI			PMID:37355986
1314125	Spopl	speckle-type BTB/POZ protein-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1314125	Spopl	speckle-type BTB/POZ protein-like	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20150430	MGI			
1314127	Arpc2	actin related protein 2/3 complex, subunit 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1314127	Arpc2	actin related protein 2/3 complex, subunit 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160804	MGI			
1314127	Arpc2	actin related protein 2/3 complex, subunit 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1314127	Arpc2	actin related protein 2/3 complex, subunit 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20141003	MGI			
1314127	Arpc2	actin related protein 2/3 complex, subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20221215	MGI			
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0011436	decreased urine magnesium level		IEA		N	RGD:5509061	20211021	MGI			
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0013621	decreased internal diameter of femur		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314129	Rin3	Ras and Rab interactor 3	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20241219	MGI			PMID:33725152
1314131	Astn2	astrotactin 2	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20180118	MGI			PMID:26418459
1314131	Astn2	astrotactin 2	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20180118	MGI			PMID:26418459
1314132	Tex261	testis expressed gene 261	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20200514	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20200514	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20200514	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200514	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20200514	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20200514	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20200514	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200514	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20200514	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1314132	Tex261	testis expressed gene 261	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20200514	MGI			
1314134	Fkrp	fukutin related protein	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20200430	MGI			PMID:26574668
1314134	Fkrp	fukutin related protein	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0002697	abnormal eye size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:26574668
1314134	Fkrp	fukutin related protein	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0003381	vitreal fibroplasia		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0004246	abnormal extensor digitorum longus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0005623	abnormal meninges morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0008030	abnormal Cajal-Retzius cell morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0009026	abnormal brain pia mater morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200430	MGI			PMID:26574668
1314134	Fkrp	fukutin related protein	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20200430	MGI			PMID:26574668
1314134	Fkrp	fukutin related protein	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20200430	MGI			PMID:26574668
1314134	Fkrp	fukutin related protein	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20200430	MGI			PMID:26574668
1314134	Fkrp	fukutin related protein	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0009959	abnormal cerebellar hemisphere morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0010235	abnormal retina inner limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24234655
1314134	Fkrp	fukutin related protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155270
1314134	Fkrp	fukutin related protein	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20675713
1314134	Fkrp	fukutin related protein	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1314134	Fkrp	fukutin related protein	gene	MP:0012031	abnormal b-wave amplitude		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0012145	increased a-wave amplitude		IAGP		N	RGD:5509061	20171214	MGI			PMID:28859131
1314134	Fkrp	fukutin related protein	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:26574668
1314134	Fkrp	fukutin related protein	gene	MP:0030265	parietal bossing		IAGP		N	RGD:5509061	20171026	MGI			PMID:20675713
1314137	Dbf4	DBF4 zinc finger	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201231	MGI			
1314137	Dbf4	DBF4 zinc finger	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314137	Dbf4	DBF4 zinc finger	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1314137	Dbf4	DBF4 zinc finger	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1314142	Cdc42ep3	CDC42 effector protein 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20221215	MGI			
1314144	Elf5	E74-like factor 5	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15650748
1314144	Elf5	E74-like factor 5	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19269284
1314144	Elf5	E74-like factor 5	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829518
1314144	Elf5	E74-like factor 5	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829518
1314144	Elf5	E74-like factor 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829518
1314144	Elf5	E74-like factor 5	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15650748
1314144	Elf5	E74-like factor 5	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19269284
1314144	Elf5	E74-like factor 5	gene	MP:0002583	absent extraembryonic ectoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829518
1314144	Elf5	E74-like factor 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829518
1314144	Elf5	E74-like factor 5	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829518
1314144	Elf5	E74-like factor 5	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19269284
1314144	Elf5	E74-like factor 5	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829518
1314144	Elf5	E74-like factor 5	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19269284
1314144	Elf5	E74-like factor 5	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829518
1314144	Elf5	E74-like factor 5	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15650748
1314144	Elf5	E74-like factor 5	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20150402	MGI			PMID:19269284
1314144	Elf5	E74-like factor 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938949
1314144	Elf5	E74-like factor 5	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15650748
1314144	Elf5	E74-like factor 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829518
1314151	Stk32c	serine/threonine kinase 32C	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1314151	Stk32c	serine/threonine kinase 32C	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201231	MGI			
1314151	Stk32c	serine/threonine kinase 32C	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1314151	Stk32c	serine/threonine kinase 32C	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20240523	MGI			
1314151	Stk32c	serine/threonine kinase 32C	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1314153	Zfp451	zinc finger protein 451	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1314153	Zfp451	zinc finger protein 451	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20160811	MGI			
1314153	Zfp451	zinc finger protein 451	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20160811	MGI			
1314153	Zfp451	zinc finger protein 451	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20250116	MGI			PMID:38600524
1314153	Zfp451	zinc finger protein 451	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20250116	MGI			PMID:37342906
1314153	Zfp451	zinc finger protein 451	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20250116	MGI			PMID:38600524
1314153	Zfp451	zinc finger protein 451	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20250116	MGI			PMID:38600524
1314153	Zfp451	zinc finger protein 451	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20250116	MGI			PMID:37342906
1314153	Zfp451	zinc finger protein 451	gene	MP:0011709	increased fibroblast cell migration		IAGP		N	RGD:5509061	20250116	MGI			PMID:38600524
1314153	Zfp451	zinc finger protein 451	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20250116	MGI			PMID:37342906
1314153	Zfp451	zinc finger protein 451	gene	MP:0014432	decreased chemokine level		IAGP		N	RGD:5509061	20250116	MGI			PMID:37342906
1314153	Zfp451	zinc finger protein 451	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20250116	MGI			PMID:38600524
1314153	Zfp451	zinc finger protein 451	gene	MP:0030678	increased hydroxyproline level		IAGP		N	RGD:5509061	20250116	MGI			PMID:38600524
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0003053	delayed tooth eruption		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314154	Sack1h	scaffolding CK1 anchoring protein H	gene	MP:0030490	periodontal pocket		IAGP		N	RGD:5509061	20180628	MGI			PMID:26788537
1314156	Snph	syntaphilin	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1314156	Snph	syntaphilin	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1314156	Snph	syntaphilin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18191227
1314156	Snph	syntaphilin	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20210128	MGI			
1314156	Snph	syntaphilin	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18191227
1314156	Snph	syntaphilin	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18191227
1314156	Snph	syntaphilin	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18191227
1314156	Snph	syntaphilin	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18191227
1314156	Snph	syntaphilin	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18191227
1314156	Snph	syntaphilin	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:32696347
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20240208	MGI			PMID:32696347
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20240208	MGI			PMID:32696347
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20240208	MGI			PMID:32696347
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:32696347
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20240208	MGI			PMID:32696347
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20240208	MGI			PMID:32696347
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20240208	MGI			PMID:32696347
1314159	Asxl3	ASXL transcriptional regulator 3	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20240208	MGI			PMID:32696347
1314161	Pcdh18	protocadherin 18	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20201231	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210128	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20160114	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160114	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20240627	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20260402	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20260402	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20150430	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0010571	shortened ST segment		IEA		N	RGD:5509061	20210128	MGI			
1314161	Pcdh18	protocadherin 18	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988498
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988498
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729948
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988498
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988498
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988498
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988498
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14988498
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314163	Tnfsf13	tumor necrosis factor (ligand) superfamily, member 13	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19016524
1314165	Naalad2	N-acetylated alpha-linked acidic dipeptidase 2	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20240718	MGI			PMID:37349952
1314165	Naalad2	N-acetylated alpha-linked acidic dipeptidase 2	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20241121	MGI			
1314165	Naalad2	N-acetylated alpha-linked acidic dipeptidase 2	gene	MP:0012306	enhanced spatial learning		IAGP		N	RGD:5509061	20240718	MGI			PMID:37349952
1314165	Naalad2	N-acetylated alpha-linked acidic dipeptidase 2	gene	MP:0030737	decreased glutamic acid level		IAGP		N	RGD:5509061	20240718	MGI			PMID:37349952
1314171	Sirt7	sirtuin 7	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18239138
1314171	Sirt7	sirtuin 7	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314171	Sirt7	sirtuin 7	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210820
1314173	Gns	glucosamine (N-acetyl)-6-sulfatase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180111	MGI			PMID:28334745
1314173	Gns	glucosamine (N-acetyl)-6-sulfatase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180111	MGI			PMID:28334745
1314173	Gns	glucosamine (N-acetyl)-6-sulfatase	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20180111	MGI			PMID:28334745
1314173	Gns	glucosamine (N-acetyl)-6-sulfatase	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:28334745
1314173	Gns	glucosamine (N-acetyl)-6-sulfatase	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:28334745
1314175	Cldn12	claudin 12	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1314175	Cldn12	claudin 12	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1314175	Cldn12	claudin 12	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0005567	decreased circulating total protein level		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1314175	Cldn12	claudin 12	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0010511	shortened PR interval		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0011954	shortened PQ interval		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314175	Cldn12	claudin 12	gene	MP:0020151	abnormal circulating non-HDL cholesterol level		IAGP		N	RGD:5509061	20191114	MGI			PMID:31511021
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20220825	MGI			PMID:23968836
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:23968836
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:23968836
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756295
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20220825	MGI			PMID:23968836
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897492
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897492
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756295
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:23968836
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20220825	MGI			PMID:23968836
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0003808	increased atrioventricular cushion size		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0003923	abnormal heart left atrium morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756295
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897492
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0005243	hemothorax		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0008727	increased heart right atrium size		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20231221	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:29659998
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0010647	heart left atrium hypoplasia		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756295
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897492
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756295
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20230601	MGI			PMID:35736367
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12756295
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897492
1314177	Carm1	coactivator-associated arginine methyltransferase 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:29659998
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20240523	MGI			
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20170105	MGI			
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20260507	MGI			PMID:36443312
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:36443312
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20260507	MGI			PMID:36443312
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0014246	decreased cellular ATP level		IAGP		N	RGD:5509061	20260507	MGI			PMID:36443312
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0014387	decreased neuron mitochondrial DNA content		IAGP		N	RGD:5509061	20260507	MGI			PMID:36443312
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0014545	increased phosphate level		IAGP		N	RGD:5509061	20260507	MGI			PMID:36443312
1314179	Cmpk2	cytidine/uridine monophosphate kinase 2	gene	MP:0030014	calcified brain		IAGP		N	RGD:5509061	20260507	MGI			PMID:36443312
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24849652
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:24849652
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160526	MGI			PMID:24849652
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1314181	Gpr107	G protein-coupled receptor 107	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314182	Pcnx2	pecanex homolog 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1314182	Pcnx2	pecanex homolog 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1314182	Pcnx2	pecanex homolog 2	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1314182	Pcnx2	pecanex homolog 2	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20170202	MGI			PMID:25010494
1314182	Pcnx2	pecanex homolog 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1314182	Pcnx2	pecanex homolog 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1314187	Sh3glb2	SH3-domain GRB2-like endophilin B2	gene	MP:0004043	abnormal pH regulation		IAGP		N	RGD:5509061	20230629	MGI			PMID:28455444
1314187	Sh3glb2	SH3-domain GRB2-like endophilin B2	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20230629	MGI			PMID:28455444
1314187	Sh3glb2	SH3-domain GRB2-like endophilin B2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20230629	MGI			PMID:28455444
1314187	Sh3glb2	SH3-domain GRB2-like endophilin B2	gene	MP:0030951	abnormal endocytosis		IAGP		N	RGD:5509061	20230629	MGI			PMID:28455444
1314192	Polr3h	polymerase (RNA) III (DNA directed) polypeptide H	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20210520	MGI			PMID:30830215
1314192	Polr3h	polymerase (RNA) III (DNA directed) polypeptide H	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20210520	MGI			PMID:30830215
1314192	Polr3h	polymerase (RNA) III (DNA directed) polypeptide H	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20210520	MGI			PMID:30830215
1314192	Polr3h	polymerase (RNA) III (DNA directed) polypeptide H	gene	MP:0008940	delayed balanopreputial separation		IAGP		N	RGD:5509061	20210520	MGI			PMID:30830215
1314192	Polr3h	polymerase (RNA) III (DNA directed) polypeptide H	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20210520	MGI			PMID:30830215
1314192	Polr3h	polymerase (RNA) III (DNA directed) polypeptide H	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20210520	MGI			PMID:30830215
1314192	Polr3h	polymerase (RNA) III (DNA directed) polypeptide H	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20210520	MGI			PMID:30830215
1314192	Polr3h	polymerase (RNA) III (DNA directed) polypeptide H	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20210520	MGI			PMID:30830215
1314195	Spire1	spire type actin nucleation factor 1	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20151231	MGI			PMID:24345451
1314195	Spire1	spire type actin nucleation factor 1	gene	MP:0009455	enhanced cued conditioning behavior		IAGP		N	RGD:5509061	20151231	MGI			PMID:24345451
1314195	Spire1	spire type actin nucleation factor 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24345451
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20150219	MGI			PMID:15866165
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393260
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0000550	abnormal forelimb morphology		IEA		N	RGD:5509061	20141003	MGI			
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20141003	MGI			
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7870176
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20141003	MGI			
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393260
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0001677	absent apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7870176
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7870176
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10489374
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20141003	MGI			
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15866165
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15866165
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20141003	MGI			
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7870176
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7870176
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0005316	abnormal response to tactile stimuli		IEA		N	RGD:5509061	20141003	MGI			
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0006302	abnormal ectomesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0006422	increased mammary adenoacanthoma incidence		IAGP		N	RGD:5509061	20150219	MGI			PMID:10489374
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22875805
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20141003	MGI			
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22875805
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7870176
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22875805
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0010318	increased salivary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10489374
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314198	Tcf7	transcription factor 7, T cell specific	gene	MP:0013166	small forelimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090727
1314199	Abca13	ATP-binding cassette, sub-family A member 13	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20250508	MGI			
1314199	Abca13	ATP-binding cassette, sub-family A member 13	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1314199	Abca13	ATP-binding cassette, sub-family A member 13	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20220901	MGI			PMID:33478937
1314199	Abca13	ATP-binding cassette, sub-family A member 13	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20220901	MGI			PMID:33478937
1314199	Abca13	ATP-binding cassette, sub-family A member 13	gene	MP:0009198	abnormal male genitalia morphology		IEA		N	RGD:5509061	20201231	MGI			
1314199	Abca13	ATP-binding cassette, sub-family A member 13	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1314199	Abca13	ATP-binding cassette, sub-family A member 13	gene	MP:0021013	abnormal synaptic vesicle endocytosis		IAGP		N	RGD:5509061	20220901	MGI			PMID:33478937
1314204	Bend7	BEN domain containing 7	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1314204	Bend7	BEN domain containing 7	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1314204	Bend7	BEN domain containing 7	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1314207	Spart	spartin	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1314207	Spart	spartin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0003707	increased cell nucleus count		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22619377
1314207	Spart	spartin	gene	MP:0010574	dilated aorta		IEA		N	RGD:5509061	20230601	MGI			
1314207	Spart	spartin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1314207	Spart	spartin	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20181227	MGI			
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1314210	Kat2b	K(lysine) acetyltransferase 2B	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1314211	Zfp771	zinc finger protein 771	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1314211	Zfp771	zinc finger protein 771	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1314211	Zfp771	zinc finger protein 771	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1314211	Zfp771	zinc finger protein 771	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1314213	Epyc	epiphycan	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160505	MGI			PMID:19932218
1314213	Epyc	epiphycan	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20160505	MGI			PMID:19932218
1314213	Epyc	epiphycan	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20160505	MGI			PMID:19932218
1314213	Epyc	epiphycan	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20190530	MGI			PMID:28864419
1314213	Epyc	epiphycan	gene	MP:0013304	osteophytes		IAGP		N	RGD:5509061	20160505	MGI			PMID:19932218
1314213	Epyc	epiphycan	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20160505	MGI			PMID:19932218
1314217	Lats2	large tumor suppressor 2	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20150910	MGI			PMID:26109051
1314217	Lats2	large tumor suppressor 2	gene	MP:0000736	delayed muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20111116	MGI			
1314217	Lats2	large tumor suppressor 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150910	MGI			PMID:26109051
1314217	Lats2	large tumor suppressor 2	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20150910	MGI			PMID:26109051
1314217	Lats2	large tumor suppressor 2	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0003707	increased cell nucleus count		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343267
1314217	Lats2	large tumor suppressor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0013182	increased spinal cord apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0013611	abnormal bile duct epithelium morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:26109051
1314217	Lats2	large tumor suppressor 2	gene	MP:0014239	abnormal intracellular organelle morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0014693	abnormal cell nucleus size		IAGP		N	RGD:5509061	20250710	MGI			PMID:17478426
1314217	Lats2	large tumor suppressor 2	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:23230145
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0009608	abnormal epidermal lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039642
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0011184	absent embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314219	Taf10	TATA-box binding protein associated factor 10	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773572
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20160602	MGI			PMID:25948814
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314221	Tnfaip8	tumor necrosis factor, alpha-induced protein 8	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1314223	Ndufb5	NADH:ubiquinone oxidoreductase subunit B5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230601	MGI			
1314225	Sorcs1	sortilin-related VPS10 domain containing receptor 1	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881129
1314227	Ap1s1	adaptor protein complex AP-1, sigma 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541143
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541143
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541143
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541143
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541143
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541143
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287179
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287179
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287179
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541143
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541143
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287179
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250220	MGI			PMID:24355749
1314229	Racgap1	Rac GTPase-activating protein 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220217	MGI			PMID:24355749
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20210805	MGI			PMID:34142127
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22484060
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15170214
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20210805	MGI			PMID:34142127
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956724
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15170214
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956724
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956724
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956724
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0004612	fusion of vertebral bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0004645	decreased vertebrae number		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:34142127
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0005222	abnormal somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0005224	abnormal left-right axis symmetry of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0005227	abnormal vertebral body development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0005229	abnormal intervertebral disk development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956724
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22326607
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956724
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641270
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:15170214
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0012669	abnormal somite segmentation clock		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314232	Hes7	hes family bHLH transcription factor 7	gene	MP:0012728	abnormal somite border morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:25248974
1314241	Pkn3	protein kinase N3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20151015	MGI			PMID:25234167
1314241	Pkn3	protein kinase N3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20151015	MGI			PMID:25234167
1314241	Pkn3	protein kinase N3	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20151015	MGI			PMID:25234167
1314241	Pkn3	protein kinase N3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151015	MGI			PMID:25234167
1314241	Pkn3	protein kinase N3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151015	MGI			PMID:25234167
1314241	Pkn3	protein kinase N3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1314241	Pkn3	protein kinase N3	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25234167
1314241	Pkn3	protein kinase N3	gene	MP:0010336	increased acute lymphoblastic leukemia incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25234167
1314241	Pkn3	protein kinase N3	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1314243	Bfsp2	beaded filament structural protein 2, phakinin	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454043
1314243	Bfsp2	beaded filament structural protein 2, phakinin	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:12573667
1314243	Bfsp2	beaded filament structural protein 2, phakinin	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12573667
1314243	Bfsp2	beaded filament structural protein 2, phakinin	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14667833
1314243	Bfsp2	beaded filament structural protein 2, phakinin	gene	MP:0003096	increased corneal light-scattering		IAGP		N	RGD:5509061	20141003	MGI			PMID:12573667
1314243	Bfsp2	beaded filament structural protein 2, phakinin	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:12573667
1314243	Bfsp2	beaded filament structural protein 2, phakinin	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:14667833
1314244	Zfp60	zinc finger protein 60	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20201022	MGI			
1314244	Zfp60	zinc finger protein 60	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1314244	Zfp60	zinc finger protein 60	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1314244	Zfp60	zinc finger protein 60	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20210826	MGI			
1314244	Zfp60	zinc finger protein 60	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940669
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077323
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0008850	increased hemoglobin concentration distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0008850	increased hemoglobin concentration distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614148
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20010697
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260507	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0014993	erythrocyte maturation arrest		IAGP		N	RGD:5509061	20260514	MGI			PMID:12077323
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:9553047
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0020431	decreased platelet alpha-granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:19927129
1314246	Zfpm1	zinc finger protein, multitype 1	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:9553047
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0003387	aorta coarctation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0006411	upturned snout		IAGP		N	RGD:5509061	20170921	MGI			PMID:19099580
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0010563	increased heart right ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0013270	fourth pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:19470456
1314249	Baz1b	bromodomain adjacent to zinc finger domain, 1B	gene	MP:0030049	prominent forehead		IAGP		N	RGD:5509061	20170921	MGI			PMID:19099580
1314255	Abca9	ATP-binding cassette, sub-family A member 9	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1314261	Pnpla3	patatin-like phospholipase domain containing 3	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20180927	MGI			PMID:24917523
1314261	Pnpla3	patatin-like phospholipase domain containing 3	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20180927	MGI			PMID:24917523
1314261	Pnpla3	patatin-like phospholipase domain containing 3	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:24917523
1314261	Pnpla3	patatin-like phospholipase domain containing 3	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20180927	MGI			PMID:24917523
1314264	Rimoc1	RAB7A interacting MON1-CCZ1 complex subunit 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20230720	MGI			
1314264	Rimoc1	RAB7A interacting MON1-CCZ1 complex subunit 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1314264	Rimoc1	RAB7A interacting MON1-CCZ1 complex subunit 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1314264	Rimoc1	RAB7A interacting MON1-CCZ1 complex subunit 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20230720	MGI			
1314264	Rimoc1	RAB7A interacting MON1-CCZ1 complex subunit 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20230720	MGI			
1314264	Rimoc1	RAB7A interacting MON1-CCZ1 complex subunit 1	gene	MP:0005533	increased body temperature		IEA		N	RGD:5509061	20230720	MGI			
1314264	Rimoc1	RAB7A interacting MON1-CCZ1 complex subunit 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230720	MGI			
1314264	Rimoc1	RAB7A interacting MON1-CCZ1 complex subunit 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20230720	MGI			
1314268	Plcl2	phospholipase C-like 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1314268	Plcl2	phospholipase C-like 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1314268	Plcl2	phospholipase C-like 2	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1314268	Plcl2	phospholipase C-like 2	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517301
1314268	Plcl2	phospholipase C-like 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517301
1314268	Plcl2	phospholipase C-like 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1314268	Plcl2	phospholipase C-like 2	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517301
1314268	Plcl2	phospholipase C-like 2	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517301
1314268	Plcl2	phospholipase C-like 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1314268	Plcl2	phospholipase C-like 2	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1314268	Plcl2	phospholipase C-like 2	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517301
1314268	Plcl2	phospholipase C-like 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1314268	Plcl2	phospholipase C-like 2	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517301
1314268	Plcl2	phospholipase C-like 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517301
1314268	Plcl2	phospholipase C-like 2	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:14517301
1314270	Rai14	retinoic acid induced 14	gene	MP:0001575	cyanosis		IEA		N	RGD:5509061	20210520	MGI			
1314270	Rai14	retinoic acid induced 14	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1314270	Rai14	retinoic acid induced 14	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1314270	Rai14	retinoic acid induced 14	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20181227	MGI			
1314270	Rai14	retinoic acid induced 14	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1314270	Rai14	retinoic acid induced 14	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314272	Ncf4	neutrophil cytosolic factor 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880254
1314272	Ncf4	neutrophil cytosolic factor 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16990793
1314272	Ncf4	neutrophil cytosolic factor 4	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880254
1314272	Ncf4	neutrophil cytosolic factor 4	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16990793
1314272	Ncf4	neutrophil cytosolic factor 4	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20181227	MGI			
1314272	Ncf4	neutrophil cytosolic factor 4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16990793
1314276	Slamf9	SLAM family member 9	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20191107	MGI			PMID:31346085
1314276	Slamf9	SLAM family member 9	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:31346085
1314276	Slamf9	SLAM family member 9	gene	MP:0008769	abnormal plasmacytoid dendritic cell physiology		IAGP		N	RGD:5509061	20191107	MGI			PMID:31346085
1314278	Efna2	ephrin A2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15713841
1314278	Efna2	ephrin A2	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16025107
1314278	Efna2	ephrin A2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20170209	MGI			PMID:10774725
1314278	Efna2	ephrin A2	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1314278	Efna2	ephrin A2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15713841
1314278	Efna2	ephrin A2	gene	MP:0002634	abnormal sensorimotor gating		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20170209	MGI			PMID:25281279
1314278	Efna2	ephrin A2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:15713841
1314280	Ift57	intraflagellar transport 57	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0004203	abnormal cranial flexure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314280	Ift57	intraflagellar transport 57	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17027958
1314282	Sec61a2	SEC61 translocon subunit alpha 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1314282	Sec61a2	SEC61 translocon subunit alpha 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909824
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0001413	abnormal response to new environment		IEA		N	RGD:5509061	20141003	MGI			
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909824
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380103
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20151112	MGI			PMID:26241864
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249187
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590044
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20171005	MGI			PMID:22465693
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20260402	MGI			
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909824
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15059932
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829020
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15059932
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15059932
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590044
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:26241864
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15059932
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380103
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20160804	MGI			
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829020
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249187
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20250508	MGI			
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590044
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829020
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004058	abnormal ventricle papillary muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004063	dilated heart left atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15059932
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20171005	MGI			PMID:22465693
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004094	abnormal M line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500336
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20171005	MGI			PMID:22465693
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829020
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590044
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829020
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20151112	MGI			PMID:26241864
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250904	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909824
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249187
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590044
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20171005	MGI			PMID:22465693
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909824
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20260402	MGI			
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829020
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15059932
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909824
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249187
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590044
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829020
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:26241864
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20141003	MGI			
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20250508	MGI			
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20250508	MGI			
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20151112	MGI			PMID:26241864
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20171005	MGI			PMID:22465693
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15059932
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0014731	disorganized myocardial fiber myofibrils		IAGP		N	RGD:5509061	20250904	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:26241864
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:11909824
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:22829020
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:10545522
1314285	Mybpc3	myosin binding protein C, cardiac	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:11909824
1314292	Pop4	processing of precursor 4, ribonuclease P/MRP family, (S. cerevisiae)	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20160107	MGI			
1314292	Pop4	processing of precursor 4, ribonuclease P/MRP family, (S. cerevisiae)	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20201231	MGI			
1314292	Pop4	processing of precursor 4, ribonuclease P/MRP family, (S. cerevisiae)	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20160107	MGI			
1314292	Pop4	processing of precursor 4, ribonuclease P/MRP family, (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314294	Tdrd6	tudor domain containing 6	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19345099
1314294	Tdrd6	tudor domain containing 6	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19345099
1314294	Tdrd6	tudor domain containing 6	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19345099
1314294	Tdrd6	tudor domain containing 6	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670278
1314294	Tdrd6	tudor domain containing 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19345099
1314294	Tdrd6	tudor domain containing 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21670278
1314294	Tdrd6	tudor domain containing 6	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19345099
1314294	Tdrd6	tudor domain containing 6	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:19345099
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20241212	MGI			PMID:36376335
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20241212	MGI			PMID:36376335
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20241212	MGI			PMID:36376335
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0004972	abnormal regulatory T cell number		IAGP		N	RGD:5509061	20241212	MGI			PMID:36376335
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20241212	MGI			PMID:36376335
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0008599	increased circulating interleukin-2 level		IAGP		N	RGD:5509061	20241212	MGI			PMID:36376335
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20241212	MGI			PMID:36376335
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0014435	increased interferon level		IAGP		N	RGD:5509061	20241212	MGI			PMID:36376335
1314295	Tnk2	tyrosine kinase, non-receptor, 2	gene	MP:0014437	increased interleukin level		IAGP		N	RGD:5509061	20241212	MGI			PMID:36376335
1314296	Mtmr10	myotubularin related protein 10	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20210121	MGI			PMID:32876667
1314296	Mtmr10	myotubularin related protein 10	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849530
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098559
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22484060
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20171102	MGI			PMID:9739106
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973278
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849530
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098559
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20171102	MGI			PMID:9739106
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973278
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098559
1314297	Mesp2	mesoderm posterior 2	gene	MP:0000963	fused dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098559
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932180
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973278
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17306789
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335362
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098559
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17306789
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15677726
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849530
1314297	Mesp2	mesoderm posterior 2	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:9739106
1314297	Mesp2	mesoderm posterior 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849530
1314297	Mesp2	mesoderm posterior 2	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0002632	vestigial tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0003794	delayed somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932180
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004600	abnormal vertebral transverse process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932180
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004604	abnormal vertebral pedicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932180
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004605	abnormal vertebral lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932180
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004605	abnormal vertebral lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973278
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098559
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098559
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849530
1314297	Mesp2	mesoderm posterior 2	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335362
1314297	Mesp2	mesoderm posterior 2	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1314297	Mesp2	mesoderm posterior 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849530
1314297	Mesp2	mesoderm posterior 2	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973278
1314297	Mesp2	mesoderm posterior 2	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973278
1314297	Mesp2	mesoderm posterior 2	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098559
1314297	Mesp2	mesoderm posterior 2	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973278
1314297	Mesp2	mesoderm posterior 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314297	Mesp2	mesoderm posterior 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0012184	absent paraxial mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1314297	Mesp2	mesoderm posterior 2	gene	MP:0012728	abnormal somite border morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11973278
1314297	Mesp2	mesoderm posterior 2	gene	MP:0012728	abnormal somite border morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17306789
1314297	Mesp2	mesoderm posterior 2	gene	MP:0012728	abnormal somite border morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242490
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0001705	abnormal proximal-distal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0001717	absent ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0002583	absent extraembryonic ectoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20200402	MGI			
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372768
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:29898916
1314305	Atad3a	ATPase family, AAA domain containing 3A	gene	MP:0014389	decreased skeletal muscle fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:29898916
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0001876	decreased inflammatory response		IEA		N	RGD:5509061	20220811	MGI			
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0003880	abnormal central pattern generator function		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0004557	dilated allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0004712	notochord degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0008503	abnormal spinal cord grey matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0011856	abnormal glomerular filtration barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1314307	Nck2	non-catalytic region of tyrosine kinase adaptor protein 2	gene	MP:0020100	decreased susceptibility to diet-induced aortic fatty streak lesions		IEA		N	RGD:5509061	20220811	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20240523	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20260402	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1314309	Klf16	Kruppel-like transcription factor 16	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1314311	Cux2	cut-like homeobox 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18223201
1314311	Cux2	cut-like homeobox 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314311	Cux2	cut-like homeobox 2	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314311	Cux2	cut-like homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033766
1314311	Cux2	cut-like homeobox 2	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033766
1314311	Cux2	cut-like homeobox 2	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314311	Cux2	cut-like homeobox 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18223201
1314311	Cux2	cut-like homeobox 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18223201
1314311	Cux2	cut-like homeobox 2	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19542352
1314311	Cux2	cut-like homeobox 2	gene	MP:0004100	abnormal spinal cord interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19542352
1314311	Cux2	cut-like homeobox 2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033766
1314311	Cux2	cut-like homeobox 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033766
1314311	Cux2	cut-like homeobox 2	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033766
1314311	Cux2	cut-like homeobox 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1314311	Cux2	cut-like homeobox 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314311	Cux2	cut-like homeobox 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314311	Cux2	cut-like homeobox 2	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314311	Cux2	cut-like homeobox 2	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314311	Cux2	cut-like homeobox 2	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033766
1314311	Cux2	cut-like homeobox 2	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1314311	Cux2	cut-like homeobox 2	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033766
1314311	Cux2	cut-like homeobox 2	gene	MP:0009689	abnormal neural tube ventricular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19542352
1314311	Cux2	cut-like homeobox 2	gene	MP:0009691	abnormal neural tube marginal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18223201
1314311	Cux2	cut-like homeobox 2	gene	MP:0009691	abnormal neural tube marginal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19542352
1314311	Cux2	cut-like homeobox 2	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314311	Cux2	cut-like homeobox 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18223201
1314311	Cux2	cut-like homeobox 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18033766
1314311	Cux2	cut-like homeobox 2	gene	MP:0020337	abnormal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314311	Cux2	cut-like homeobox 2	gene	MP:0021090	abnormal dendrite arborization pattern		IAGP		N	RGD:5509061	20230413	MGI			PMID:35379703
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:26720614
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33682352
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0001714	absent trophoblast giant cells		IAGP		N	RGD:5509061	20210506	MGI			PMID:33682352
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20210506	MGI			PMID:33682352
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210506	MGI			PMID:33682352
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20210506	MGI			PMID:33682352
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210506	MGI			PMID:33682352
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20210506	MGI			PMID:33682352
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210506	MGI			PMID:33682352
1314315	Vps4b	vacuolar protein sorting 4B	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20210506	MGI			PMID:33682352
1314317	Cd68	CD68 antigen	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991369
1314317	Cd68	CD68 antigen	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991369
1314317	Cd68	CD68 antigen	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991369
1314317	Cd68	CD68 antigen	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21572087
1314317	Cd68	CD68 antigen	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991369
1314317	Cd68	CD68 antigen	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991369
1314317	Cd68	CD68 antigen	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991369
1314317	Cd68	CD68 antigen	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991369
1314317	Cd68	CD68 antigen	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1314317	Cd68	CD68 antigen	gene	MP:0020080	increased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:21991369
1314319	Lsm3	LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated	gene	MP:0008573	increased circulating interferon-alpha level		IAGP		N	RGD:5509061	20180830	MGI			PMID:29706547
1314319	Lsm3	LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20180830	MGI			PMID:29706547
1314319	Lsm3	LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20180830	MGI			PMID:29706547
1314319	Lsm3	LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:29706547
1314319	Lsm3	LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:29706547
1314319	Lsm3	LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated	gene	MP:0031023	decreased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:29706547
1314322	Sectm1a	secreted and transmembrane 1A	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20220127	MGI			PMID:32170929
1314322	Sectm1a	secreted and transmembrane 1A	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20220127	MGI			PMID:32170929
1314322	Sectm1a	secreted and transmembrane 1A	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20220127	MGI			PMID:32170929
1314322	Sectm1a	secreted and transmembrane 1A	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20220127	MGI			PMID:32170929
1314322	Sectm1a	secreted and transmembrane 1A	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20220127	MGI			PMID:32170929
1314322	Sectm1a	secreted and transmembrane 1A	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20220127	MGI			PMID:32170929
1314322	Sectm1a	secreted and transmembrane 1A	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20220127	MGI			PMID:32170929
1314322	Sectm1a	secreted and transmembrane 1A	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20220127	MGI			PMID:32170929
1314322	Sectm1a	secreted and transmembrane 1A	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20220127	MGI			PMID:32170929
1314325	Efr3a	EFR3 homolog A	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20190919	MGI			PMID:28193719
1314325	Efr3a	EFR3 homolog A	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20190919	MGI			PMID:28193719
1314327	Thbs3	thrombospondin 3	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964815
1314327	Thbs3	thrombospondin 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964815
1314327	Thbs3	thrombospondin 3	gene	MP:0003416	premature bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964815
1314329	Glipr1	GLI pathogenesis related 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199537
1314329	Glipr1	GLI pathogenesis related 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230601	MGI			
1314329	Glipr1	GLI pathogenesis related 1	gene	MP:0008403	decreased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:18199537
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:12644183
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:1339316
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:5556347
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:9071596
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:9475750
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000019	thick ears		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000022	abnormal ear shape		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000024	lowered ear position		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000097	short maxilla		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664685
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1339316
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664685
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:13563786
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0001394	circling		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:5021246
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5021246
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664685
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664685
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12644183
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002102	abnormal ear morphology		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002177	abnormal outer ear morphology		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002233	abnormal nose morphology		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002249	abnormal larynx morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002256	abnormal laryngeal cartilage morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20190523	MGI			PMID:20284341
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0002999	abnormal bone healing		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003230	abnormal umbilical artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1339316
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20190523	MGI			PMID:20284341
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003585	large ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004350	long humerus		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004357	long tibia		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004360	absent ulna		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664685
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004680	small xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664685
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004695	increased length of long bones		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0004880	lung cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1339316
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0006325	impaired hearing		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0008150	decreased diameter of long bones		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0008150	decreased diameter of long bones		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0008154	decreased diameter of humerus		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:13563786
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664685
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0008525	decreased cranium height		IEA		N	RGD:5509061	20111116	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0009005	abnormal sesamoid bone of gastrocnemius morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5021246
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0010031	abnormal cranium size		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0010113	abnormal sacrum morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5021246
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0010770	preweaning lethality		IEA		N	RGD:5509061	20111229	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1339316
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5556347
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5021246
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0011318	abnormal right renal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0011727	ectopic ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0011835	abnormal urogenital fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5692092
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0011872	absent xiphoid process		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0020084	short ears		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0020084	short ears		IAGP		N	RGD:5509061	20170914	MGI			PMID:1339316
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0020084	short ears		IAGP		N	RGD:5509061	20170914	MGI			PMID:5556347
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0020084	short ears		IAGP		N	RGD:5509061	20180315	MGI			PMID:7710253
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0030422	abnormal outer ear cartilage morphology		IEA		N	RGD:5509061	20171214	MGI			
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0030872	small cricoid cartilage		IAGP		N	RGD:5509061	20230601	MGI			PMID:24539717
1314331	Bmp5	bone morphogenetic protein 5	gene	MP:0031286	unilateral cryptorchism		IAGP		N	RGD:5509061	20211014	MGI			PMID:5692092
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20181227	MGI			
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748381
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748381
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748381
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748381
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748381
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20181227	MGI			
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748381
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748381
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748381
1314333	Mbd1	methyl-CpG binding domain protein 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748381
1314336	Ciao3	cytosolic iron-sulfur assembly component 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21367862
1314336	Ciao3	cytosolic iron-sulfur assembly component 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21367862
1314336	Ciao3	cytosolic iron-sulfur assembly component 3	gene	MP:0006205	embryonic lethality between implantation and somite formation		IEA		N	RGD:5509061	20141003	MGI			
1314336	Ciao3	cytosolic iron-sulfur assembly component 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21367862
1314336	Ciao3	cytosolic iron-sulfur assembly component 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21367862
1314338	Pttg1ip	pituitary tumor-transforming 1 interacting protein	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1314338	Pttg1ip	pituitary tumor-transforming 1 interacting protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1314338	Pttg1ip	pituitary tumor-transforming 1 interacting protein	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1314338	Pttg1ip	pituitary tumor-transforming 1 interacting protein	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1314338	Pttg1ip	pituitary tumor-transforming 1 interacting protein	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1314338	Pttg1ip	pituitary tumor-transforming 1 interacting protein	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767157
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767157
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767157
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522945
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522945
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522945
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767157
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522945
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767157
1314342	Suds3	suppressor of defective silencing 3 homolog (S. cerevisiae)	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14522945
1314348	Dusp15	dual specificity phosphatase-like 15	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1314348	Dusp15	dual specificity phosphatase-like 15	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1314350	Procr	protein C receptor, endothelial	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218060
1314350	Procr	protein C receptor, endothelial	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218060
1314350	Procr	protein C receptor, endothelial	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218060
1314350	Procr	protein C receptor, endothelial	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12353077
1314350	Procr	protein C receptor, endothelial	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956290
1314350	Procr	protein C receptor, endothelial	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218060
1314350	Procr	protein C receptor, endothelial	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023579
1314350	Procr	protein C receptor, endothelial	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956290
1314350	Procr	protein C receptor, endothelial	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023579
1314350	Procr	protein C receptor, endothelial	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218060
1314350	Procr	protein C receptor, endothelial	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956290
1314350	Procr	protein C receptor, endothelial	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023579
1314350	Procr	protein C receptor, endothelial	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218060
1314350	Procr	protein C receptor, endothelial	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956290
1314350	Procr	protein C receptor, endothelial	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160128	MGI			PMID:25327250
1314350	Procr	protein C receptor, endothelial	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956290
1314350	Procr	protein C receptor, endothelial	gene	MP:0012330	decreased circulating fibrinogen level		IAGP		N	RGD:5509061	20200618	MGI			PMID:15956290
1314350	Procr	protein C receptor, endothelial	gene	MP:0013776	bone marrow failure		IAGP		N	RGD:5509061	20160922	MGI			PMID:26045607
1314350	Procr	protein C receptor, endothelial	gene	MP:0020407	abnormal placental thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:12218060
1314350	Procr	protein C receptor, endothelial	gene	MP:0031059	increased circulating C-reactive protein level		IAGP		N	RGD:5509061	20200618	MGI			PMID:15956290
1314350	Procr	protein C receptor, endothelial	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200924	MGI			PMID:26045607
1314353	Trim46	tripartite motif-containing 46	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1314353	Trim46	tripartite motif-containing 46	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1314353	Trim46	tripartite motif-containing 46	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1314353	Trim46	tripartite motif-containing 46	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20220519	MGI			
1314353	Trim46	tripartite motif-containing 46	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220519	MGI			
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20171026	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21089073
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454269
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773491
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454269
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452853
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20730911
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000508	right-sided isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000508	right-sided isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454269
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773491
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773491
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773491
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302604
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7924997
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20190228	MGI			PMID:8429908
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302604
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7924997
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452853
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001705	abnormal proximal-distal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302604
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773491
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001710	absent amniotic folds		IAGP		N	RGD:5509061	20141003	MGI			PMID:7924997
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302604
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950123
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:7924997
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302604
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7924997
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7924997
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454269
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736223
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773491
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002174	abnormal gastrulation movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950123
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0002844	aortic hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1314355	Nodal	nodal growth differentiation factor	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11456449
1314355	Nodal	nodal growth differentiation factor	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1314355	Nodal	nodal growth differentiation factor	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1314355	Nodal	nodal growth differentiation factor	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454269
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773491
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454269
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466485
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773491
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11456449
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004387	abnormal prechordal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004387	abnormal prechordal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004388	absent prechordal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004388	absent prechordal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004714	truncated notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004714	truncated notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452853
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20201231	MGI			
1314355	Nodal	nodal growth differentiation factor	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0006061	right atrial isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1314355	Nodal	nodal growth differentiation factor	gene	MP:0006323	abnormal extraembryonic mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7924997
1314355	Nodal	nodal growth differentiation factor	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23221368
1314355	Nodal	nodal growth differentiation factor	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0008786	abnormal hindgut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1314355	Nodal	nodal growth differentiation factor	gene	MP:0008926	abnormal anterior definitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1314355	Nodal	nodal growth differentiation factor	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950123
1314355	Nodal	nodal growth differentiation factor	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1314355	Nodal	nodal growth differentiation factor	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20170314	MGI			PMID:27466203
1314355	Nodal	nodal growth differentiation factor	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11456449
1314355	Nodal	nodal growth differentiation factor	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20171026	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010126	abnormal distal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302604
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010335	fused first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010335	fused first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454269
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7924997
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010807	abnormal stomach position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0010807	abnormal stomach position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12231623
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8610012
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452853
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950123
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654299
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011203	abnormal parietal yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011206	absent visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011255	abnormal anterior visceral endoderm cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11456449
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012081	absent heart tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454269
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012083	absent foregut		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012084	truncated foregut		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012098	increased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11456449
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452853
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012156	rostral-caudal axis duplication		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302604
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9655392
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20170314	MGI			PMID:27466203
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012160	expanded anterior visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20171109	MGI			PMID:11311163
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012181	increased somite number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012515	abnormal heart apex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091315
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842913
1314355	Nodal	nodal growth differentiation factor	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879365
1314355	Nodal	nodal growth differentiation factor	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1314355	Nodal	nodal growth differentiation factor	gene	MP:0030198	nasal septum hypoplasia		IAGP		N	RGD:5509061	20171012	MGI			PMID:16564040
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357274
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829970
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829970
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829970
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769945
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088088
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0003684	abnormal inferior olivary complex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829970
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0004165	abnormal lateral geniculate nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357274
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829970
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769945
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769945
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829970
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088088
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18829970
1314359	Olig3	oligodendrocyte transcription factor 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357274
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273653
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11549709
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11549709
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273653
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273653
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273653
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273653
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273653
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11549709
1314361	Klk8	kallikrein related-peptidase 8	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11273653
1314363	Csrnp1	cysteine-serine-rich nuclear protein 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314363	Csrnp1	cysteine-serine-rich nuclear protein 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314363	Csrnp1	cysteine-serine-rich nuclear protein 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17726538
1314363	Csrnp1	cysteine-serine-rich nuclear protein 1	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314363	Csrnp1	cysteine-serine-rich nuclear protein 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314363	Csrnp1	cysteine-serine-rich nuclear protein 1	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314363	Csrnp1	cysteine-serine-rich nuclear protein 1	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314363	Csrnp1	cysteine-serine-rich nuclear protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17726538
1314363	Csrnp1	cysteine-serine-rich nuclear protein 1	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:17143286
1314367	Tnn	tenascin N	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0000119	abnormal tooth eruption		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1314367	Tnn	tenascin N	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230601	MGI			
1314367	Tnn	tenascin N	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0013250	abnormal dental pulp morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0030131	abnormal periodontium morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0030456	abnormal odontoblast differentiation		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0030471	abnormal ameloblast differentiation		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0030508	abnormal dental epithelium morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0030542	abnormal dentin development		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314367	Tnn	tenascin N	gene	MP:0030544	abnormal enamel development		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0000592	short tail		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0001915	intracranial hemorrhage		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20250508	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0006301	abnormal mesenchyme morphology		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0009698	heart hemorrhage		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0012098	increased spongiotrophoblast size		IEA		N	RGD:5509061	20251204	MGI			
1314370	Alg3	ALG3 alpha-1,3- mannosyltransferase	gene	MP:0013176	abnormal tail position or orientation		IEA		N	RGD:5509061	20251204	MGI			
1314371	Slc38a11	solute carrier family 38, member 11	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20231207	MGI			
1314373	Brms1l	breast cancer metastasis-suppressor 1-like	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20240523	MGI			
1314373	Brms1l	breast cancer metastasis-suppressor 1-like	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20240523	MGI			
1314373	Brms1l	breast cancer metastasis-suppressor 1-like	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20201022	MGI			
1314373	Brms1l	breast cancer metastasis-suppressor 1-like	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1314373	Brms1l	breast cancer metastasis-suppressor 1-like	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1314377	Armc12	armadillo repeat containing 12	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1314377	Armc12	armadillo repeat containing 12	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1314377	Armc12	armadillo repeat containing 12	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1314377	Armc12	armadillo repeat containing 12	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1314377	Armc12	armadillo repeat containing 12	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20240613	MGI			PMID:33536340
1314377	Armc12	armadillo repeat containing 12	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1314377	Armc12	armadillo repeat containing 12	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1314377	Armc12	armadillo repeat containing 12	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1314382	Rnf126	ring finger protein 126	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1314382	Rnf126	ring finger protein 126	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20240822	MGI			PMID:36563124
1314382	Rnf126	ring finger protein 126	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20240822	MGI			PMID:36563124
1314382	Rnf126	ring finger protein 126	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1314382	Rnf126	ring finger protein 126	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240822	MGI			PMID:36563124
1314382	Rnf126	ring finger protein 126	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1314382	Rnf126	ring finger protein 126	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20240822	MGI			PMID:36563124
1314384	Tsga13	testis specific gene A13	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20220811	MGI			
1314384	Tsga13	testis specific gene A13	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1314384	Tsga13	testis specific gene A13	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1314386	Scarf2	scavenger receptor class F, member 2	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20160114	MGI			
1314391	Myo1g	myosin IG	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1314391	Myo1g	myosin IG	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1314391	Myo1g	myosin IG	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:25083865
1314391	Myo1g	myosin IG	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24310084
1314391	Myo1g	myosin IG	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20230601	MGI			
1314391	Myo1g	myosin IG	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24310084
1314391	Myo1g	myosin IG	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24310084
1314391	Myo1g	myosin IG	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1314391	Myo1g	myosin IG	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24310084
1314391	Myo1g	myosin IG	gene	MP:0014472	impaired B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:24310084
1314396	Alppl2	alkaline phosphatase, placental-like 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10767088
1314396	Alppl2	alkaline phosphatase, placental-like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9056646
1314396	Alppl2	alkaline phosphatase, placental-like 2	gene	MP:0002293	long gestation period		IAGP		N	RGD:5509061	20141003	MGI			PMID:10767088
1314396	Alppl2	alkaline phosphatase, placental-like 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10767088
1314396	Alppl2	alkaline phosphatase, placental-like 2	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10767088
1314396	Alppl2	alkaline phosphatase, placental-like 2	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10767088
1314402	Dnajc8	DnaJ heat shock protein family (Hsp40) member C8	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1314402	Dnajc8	DnaJ heat shock protein family (Hsp40) member C8	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1314402	Dnajc8	DnaJ heat shock protein family (Hsp40) member C8	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1314402	Dnajc8	DnaJ heat shock protein family (Hsp40) member C8	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1314402	Dnajc8	DnaJ heat shock protein family (Hsp40) member C8	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1314402	Dnajc8	DnaJ heat shock protein family (Hsp40) member C8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314402	Dnajc8	DnaJ heat shock protein family (Hsp40) member C8	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1314404	Naga	N-acetyl galactosaminidase, alpha	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20201022	MGI			
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359245
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0002944	increased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0003062	abnormal coping response		IEA		N	RGD:5509061	20160804	MGI			
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20160804	MGI			
1314408	Epc1	enhancer of polycomb homolog 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359245
1314409	Aifm3	apoptosis-inducing factor, mitochondrion-associated 3	gene	MP:0000181	abnormal circulating LDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1314409	Aifm3	apoptosis-inducing factor, mitochondrion-associated 3	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20211021	MGI			
1314409	Aifm3	apoptosis-inducing factor, mitochondrion-associated 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1314409	Aifm3	apoptosis-inducing factor, mitochondrion-associated 3	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20181227	MGI			
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20181227	MGI			
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20181227	MGI			
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0001956	hypopnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0003005	abnormal hippocampal fimbria morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964824
1314411	Klf7	Kruppel-like transcription factor 7 (ubiquitous)	gene	MP:0014750	abnormal retinal ganglion cell axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:15964824
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281502
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281502
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0008121	increased myeloid dendritic cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0010963	abnormal compact bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0013693	abnormal hemopoiesis		IAGP		N	RGD:5509061	20161124	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0030007	abnormal bone marrow adipose tissue morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0030009	increased bone marrow adipose tissue amount		IAGP		N	RGD:5509061	20170706	MGI			PMID:27445989
1314414	Mfap2	microfibrillar-associated protein 2	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:18281502
1314420	Epb41l4a	erythrocyte membrane protein band 4.1 like 4a	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1314420	Epb41l4a	erythrocyte membrane protein band 4.1 like 4a	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1314420	Epb41l4a	erythrocyte membrane protein band 4.1 like 4a	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210826	MGI			
1314420	Epb41l4a	erythrocyte membrane protein band 4.1 like 4a	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1314420	Epb41l4a	erythrocyte membrane protein band 4.1 like 4a	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210520	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0000826	abnormal third ventricle morphology		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0003253	dilated bile duct		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0003595	epididymal cyst		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0005274	abnormal viscerocranium morphology		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0008922	abnormal cervical rib		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0009493	abnormal cystic duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0009532	decreased parotid gland size		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0010727	increased glioblastoma incidence		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0011536	decreased urination frequency		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200806	MGI			PMID:31677819
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0013975	abnormal coronary sinus connection		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0014018	embryo tumor		IEA		N	RGD:5509061	20170504	MGI			
1314426	Coro1c	coronin, actin binding protein 1C	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1314428	C1ql1	complement component 1, q subcomponent-like 1	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1314428	C1ql1	complement component 1, q subcomponent-like 1	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1314428	C1ql1	complement component 1, q subcomponent-like 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1314428	C1ql1	complement component 1, q subcomponent-like 1	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1314428	C1ql1	complement component 1, q subcomponent-like 1	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1314431	Ttc38	tetratricopeptide repeat domain 38	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803355
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20151217	MGI			PMID:22932389
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20151217	MGI			PMID:22932389
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20151217	MGI			PMID:22932389
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803355
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0003880	abnormal central pattern generator function		IAGP		N	RGD:5509061	20151217	MGI			PMID:22932389
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0003936	abnormal reproductive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803355
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0004100	abnormal spinal cord interneuron morphology		IAGP		N	RGD:5509061	20151217	MGI			PMID:22932389
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20151217	MGI			PMID:22932389
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056351
1314435	Dmrt3	doublesex and mab-3 related transcription factor 3	gene	MP:0010540	long stride length		IAGP		N	RGD:5509061	20151217	MGI			PMID:22932389
1314441	Reep5	receptor accessory protein 5	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1314444	Smox	spermine oxidase	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170323	MGI			
1314446	Gdap2	ganglioside-induced differentiation-associated-protein 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1314446	Gdap2	ganglioside-induced differentiation-associated-protein 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1314446	Gdap2	ganglioside-induced differentiation-associated-protein 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20181227	MGI			
1314446	Gdap2	ganglioside-induced differentiation-associated-protein 2	gene	MP:0005478	decreased circulating thyroxine level		IEA		N	RGD:5509061	20181227	MGI			
1314446	Gdap2	ganglioside-induced differentiation-associated-protein 2	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20211021	MGI			
1314446	Gdap2	ganglioside-induced differentiation-associated-protein 2	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20201231	MGI			
1314446	Gdap2	ganglioside-induced differentiation-associated-protein 2	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20210128	MGI			
1314446	Gdap2	ganglioside-induced differentiation-associated-protein 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200402	MGI			
1314446	Gdap2	ganglioside-induced differentiation-associated-protein 2	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20181227	MGI			
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0002708	nephrolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0009810	increased urine uric acid level		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0010092	increased circulating magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0011423	kidney cortex atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0011435	increased urine magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0011537	uraturia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706426
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314451	Slc2a9	solute carrier family 2 (facilitated glucose transporter), member 9	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20160428	MGI			PMID:25100214
1314453	Pea15a	proliferation and apoptosis adaptor protein 15A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10493725
1314453	Pea15a	proliferation and apoptosis adaptor protein 15A	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10493725
1314453	Pea15a	proliferation and apoptosis adaptor protein 15A	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:17504918
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0003948	abnormal gas homeostasis		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0004848	abnormal liver size		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314454	Helz2	helicase with zinc finger 2, transcriptional coactivator	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20160218	MGI			PMID:25004093
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16815997
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16815997
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16815997
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854161
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0008221	abnormal hippocampal commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0008583	absent photoreceptor inner segment		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0010011	ectopic hippocampus pyramidal cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16815997
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0012194	decreased keratinocyte migration		IAGP		N	RGD:5509061	20141204	MGI			PMID:18854161
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0013908	small lateral ventricles		IAGP		N	RGD:5509061	20161103	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:20170731
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0020439	absent b-wave		IAGP		N	RGD:5509061	20200123	MGI			PMID:27783952
1314455	Macf1	microtubule-actin crosslinking factor 1	gene	MP:0030577	increased keratinocyte adhesion		IAGP		N	RGD:5509061	20180607	MGI			PMID:18854161
1314458	Onecut3	one cut domain, family member 3	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400205
1314458	Onecut3	one cut domain, family member 3	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400205
1314458	Onecut3	one cut domain, family member 3	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400205
1314460	Pgm2	phosphoglucomutase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:162283
1314460	Pgm2	phosphoglucomutase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:6457600
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20241010	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0002582	disorganized extraembryonic tissue		IEA		N	RGD:5509061	20241010	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241010	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20230601	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230601	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20230601	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230601	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1314462	Skic3	SKI3 subunit of superkiller complex	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
1314463	Cep15	centrosomal protein 15	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230720	MGI			
1314464	Dennd6a	DENN domain containing 6A	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1314469	Esf1	ESF1 nucleolar pre-rRNA processing protein homolog	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20260402	MGI			
1314469	Esf1	ESF1 nucleolar pre-rRNA processing protein homolog	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20260402	MGI			
1314469	Esf1	ESF1 nucleolar pre-rRNA processing protein homolog	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20260402	MGI			
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16157885
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20220915	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:17227869
1314471	Arhgap1	Rho GTPase activating protein 1	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:17227869
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:22741057
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220407	MGI			PMID:22741057
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20231207	MGI			
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20220224	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:22741057
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220519	MGI			
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0014011	abnormal ovary tissue architecture		IAGP		N	RGD:5509061	20220407	MGI			PMID:22741057
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0014443	impaired polar body extrusion		IAGP		N	RGD:5509061	20240509	MGI			PMID:21277975
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19696012
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
1314473	Vrk1	vaccinia related kinase 1	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:22741057
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10802659
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300562
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0001326	retina degeneration		IEA		N	RGD:5509061	20111116	MGI			
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300562
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10802659
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300562
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10802659
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10802659
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10802659
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300562
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300562
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300562
1314475	Rom1	rod outer segment membrane protein 1	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20300562
1314477	Inpp1	inositol polyphosphate-1-phosphatase	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20160804	MGI			
1314477	Inpp1	inositol polyphosphate-1-phosphatase	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1314477	Inpp1	inositol polyphosphate-1-phosphatase	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1314477	Inpp1	inositol polyphosphate-1-phosphatase	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
1314477	Inpp1	inositol polyphosphate-1-phosphatase	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314477	Inpp1	inositol polyphosphate-1-phosphatase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20201022	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201022	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20201022	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20201022	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0008966	abnormal chiasmata formation		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20201022	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20201022	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:32463460
1314478	Brme1	break repair meiotic recombinase recruitment factor 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:32463460
1314479	Obsl1	obscurin-like 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0002713	abnormal glycogen catabolism		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0009423	increased extensor digitorum longus weight		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0012655	increased catalase level		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:31098411
1314479	Obsl1	obscurin-like 1	gene	MP:0014775	decreased skeletal muscle enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:31098411
1314480	Mymk	myomaker, myoblast fusion factor	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23868259
1314480	Mymk	myomaker, myoblast fusion factor	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23868259
1314480	Mymk	myomaker, myoblast fusion factor	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23868259
1314480	Mymk	myomaker, myoblast fusion factor	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23868259
1314480	Mymk	myomaker, myoblast fusion factor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23868259
1314480	Mymk	myomaker, myoblast fusion factor	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23868259
1314480	Mymk	myomaker, myoblast fusion factor	gene	MP:0030959	abnormal myoblast fusion		IAGP		N	RGD:5509061	20190725	MGI			PMID:23868259
1314482	Srp72	signal recognition particle 72	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1314482	Srp72	signal recognition particle 72	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230119	MGI			
1314482	Srp72	signal recognition particle 72	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230119	MGI			
1314482	Srp72	signal recognition particle 72	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20250508	MGI			
1314482	Srp72	signal recognition particle 72	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230119	MGI			
1314482	Srp72	signal recognition particle 72	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1314482	Srp72	signal recognition particle 72	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230119	MGI			
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20160804	MGI			PMID:22914735
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314486	Neil1	nei endonuclease VIII-like 1 (E. coli)	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16446448
1314488	Cyp2s1	cytochrome P450, family 2, subfamily s, polypeptide 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23073733
1314491	Blvrb	biliverdin reductase B	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
1314491	Blvrb	biliverdin reductase B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1314491	Blvrb	biliverdin reductase B	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1314494	Cabp4	calcium binding protein 4	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1314494	Cabp4	calcium binding protein 4	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20181227	MGI			
1314494	Cabp4	calcium binding protein 4	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20181227	MGI			
1314494	Cabp4	calcium binding protein 4	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15452577
1314494	Cabp4	calcium binding protein 4	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:15452577
1314500	Riok1	RIO kinase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314500	Riok1	RIO kinase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1314500	Riok1	RIO kinase 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240801	MGI			
1314502	Auh	AU RNA binding protein/enoyl-coenzyme A hydratase	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20181227	MGI			
1314502	Auh	AU RNA binding protein/enoyl-coenzyme A hydratase	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1314502	Auh	AU RNA binding protein/enoyl-coenzyme A hydratase	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20221215	MGI			
1314504	Sfxn4	sideroflexin 4	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20211028	MGI			PMID:27270835
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20211028	MGI			PMID:27270835
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20211028	MGI			PMID:27270835
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0001785	edema		IEA		N	RGD:5509061	20221215	MGI			
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20221215	MGI			
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20211028	MGI			PMID:27270835
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0009022	abnormal brain meninges morphology		IAGP		N	RGD:5509061	20211028	MGI			PMID:27270835
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20211028	MGI			PMID:27270835
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20211028	MGI			PMID:27270835
1314510	Arhgap31	Rho GTPase activating protein 31	gene	MP:0031152	subcutaneous hemorrhage		IAGP		N	RGD:5509061	20211028	MGI			PMID:27270835
1314516	Dop1b	DOP1 leucine zipper like protein B	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20150108	MGI			
1314516	Dop1b	DOP1 leucine zipper like protein B	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1314516	Dop1b	DOP1 leucine zipper like protein B	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201022	MGI			
1314516	Dop1b	DOP1 leucine zipper like protein B	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20211021	MGI			
1314516	Dop1b	DOP1 leucine zipper like protein B	gene	MP:0003442	decreased circulating glycerol level		IEA		N	RGD:5509061	20150108	MGI			
1314516	Dop1b	DOP1 leucine zipper like protein B	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1314516	Dop1b	DOP1 leucine zipper like protein B	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1314516	Dop1b	DOP1 leucine zipper like protein B	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1314516	Dop1b	DOP1 leucine zipper like protein B	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1314517	Sae1	SUMO1 activating enzyme subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0000489	abnormal large intestine morphology		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0000496	abnormal small intestine morphology		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0001879	abnormal lymphatic vessel morphology		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0002951	small thyroid gland		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0003262	intestinal/bowel diverticulum		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0009820	abnormal liver vasculature morphology		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0013963	jugular vein stenosis		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0013975	abnormal coronary sinus connection		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0014018	embryo tumor		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0014019	embryo cyst		IEA		N	RGD:5509061	20170504	MGI			
1314521	Cmip	c-Maf inducing protein	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0001340	abnormal eyelid morphology		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200514	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31026345
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20201015	MGI			PMID:31026345
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0004065	increased susceptibility to induced muscular atrophy		IAGP		N	RGD:5509061	20201015	MGI			PMID:31026345
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20201015	MGI			PMID:31026345
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0005176	eyelids fail to open		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0005544	cornea deposits		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0006241	abnormal placement of pupils		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20201015	MGI			PMID:31026345
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20201015	MGI			PMID:31026345
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:31026345
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:31026345
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0012121	sclerocornea		IEA		N	RGD:5509061	20260402	MGI			
1314536	Eif3f	eukaryotic translation initiation factor 3, subunit F	gene	MP:0031739	impaired translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:31026345
1314538	Fjx1	four jointed box 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18604206
1314538	Fjx1	four jointed box 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20241121	MGI			
1314538	Fjx1	four jointed box 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028897
1314538	Fjx1	four jointed box 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18604206
1314538	Fjx1	four jointed box 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18604206
1314538	Fjx1	four jointed box 1	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18604206
1314538	Fjx1	four jointed box 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903076
1314538	Fjx1	four jointed box 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028897
1314538	Fjx1	four jointed box 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18604206
1314538	Fjx1	four jointed box 1	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:18604206
1314543	Fhip2a	FHF complex subunit HOOK interacting protein 2A	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230601	MGI			
1314543	Fhip2a	FHF complex subunit HOOK interacting protein 2A	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1314543	Fhip2a	FHF complex subunit HOOK interacting protein 2A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1314543	Fhip2a	FHF complex subunit HOOK interacting protein 2A	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1314543	Fhip2a	FHF complex subunit HOOK interacting protein 2A	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20230601	MGI			
1314543	Fhip2a	FHF complex subunit HOOK interacting protein 2A	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20230601	MGI			
1314546	Enox1	ecto-NOX disulfide-thiol exchanger 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1314546	Enox1	ecto-NOX disulfide-thiol exchanger 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20221215	MGI			
1314546	Enox1	ecto-NOX disulfide-thiol exchanger 1	gene	MP:0011954	shortened PQ interval		IEA		N	RGD:5509061	20220519	MGI			
1314548	Mideas	mitotic deacetylase associated SANT domain protein	gene	MP:0000215	absent erythrocytes		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1314548	Mideas	mitotic deacetylase associated SANT domain protein	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1314548	Mideas	mitotic deacetylase associated SANT domain protein	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1314548	Mideas	mitotic deacetylase associated SANT domain protein	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1314548	Mideas	mitotic deacetylase associated SANT domain protein	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1314548	Mideas	mitotic deacetylase associated SANT domain protein	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1314548	Mideas	mitotic deacetylase associated SANT domain protein	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19906844
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20570969
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000075	absent neurocranium		IAGP		N	RGD:5509061	20171102	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15728667
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19549984
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19549984
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000288	abnormal pericardium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20170209	MGI			PMID:18397875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000413	polyphalangy		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000413	polyphalangy		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:23645682
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20170209	MGI			PMID:19906844
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000561	adactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:10725236
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:11748151
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:12385751
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:12435627
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:17266131
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:17504940
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:19223390
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:19549984
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:1983115
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:20386744
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:22465667
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:24700818
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:6062373
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:7628698
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268572
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20386744
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268572
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:7976186
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9232833
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20170209	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20190228	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:7976186
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:7976186
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20170209	MGI			PMID:19549984
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20170209	MGI			PMID:22383895
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22698544
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20170209	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20170209	MGI			PMID:7976186
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20170209	MGI			PMID:18397875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20170209	MGI			PMID:7976186
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000935	abnormal folding of telencephalic vesicles		IAGP		N	RGD:5509061	20170209	MGI			PMID:7976186
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20170209	MGI			PMID:15215207
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16720875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170209	MGI			PMID:19906844
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001678	thick apical ectodermal ridge		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001699	increased embryo size		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268579
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20170209	MGI			PMID:19549984
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268579
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20170209	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170209	MGI			PMID:11748151
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20170209	MGI			
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20170209	MGI			PMID:18397875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:11748151
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16720875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22465667
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6062373
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20170209	MGI			PMID:12435627
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19666503
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12385751
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22465667
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20170209	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002256	abnormal laryngeal cartilage morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20170209	MGI			PMID:6062373
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20170209	MGI			PMID:7976186
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20170209	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002671	belted		IAGP		N	RGD:5509061	20170209	MGI			PMID:18397875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003006	abnormal hippocampal fornix morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003069	abnormal superior semicircular canal morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003130	anal atresia		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003160	abnormal esophagus development		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20170209	MGI			PMID:22383895
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20170209	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20170209	MGI			PMID:7976186
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20170209	MGI			PMID:9232833
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268579
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9232833
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003841	abnormal lambdoid suture morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20570969
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20386744
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20386744
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:19223390
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:6062373
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004135	abnormal mammary gland embryonic development		IAGP		N	RGD:5509061	20170209	MGI			PMID:16914490
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19906844
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20170209	MGI			PMID:15728667
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20170209	MGI			PMID:15728667
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004360	absent ulna		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004372	bowed fibula		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004457	abnormal orbitosphenoid bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004506	abnormal pubis morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004537	abnormal palatine bone horizontal plate morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004544	absent esophagus		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004576	abnormal embryonic autopod plate morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20170209	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005237	abnormal olfactory tract morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6062373
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005313	absent adrenal gland		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20170209	MGI			PMID:18397875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268579
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20170209	MGI			PMID:9232833
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20170209	MGI			PMID:9232833
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20170209	MGI			PMID:20386744
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20170209	MGI			PMID:1983115
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0006292	abnormal nasal placode morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19906844
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0006343	enlarged first pharyngeal arch		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008161	increased diameter of radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008163	increased diameter of ulna		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20170209	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20170209	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008275	failure of endochondral bone ossification		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:2323034
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:7976186
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20170209	MGI			PMID:18397875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22383895
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008818	abnormal interfrontal bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008818	abnormal interfrontal bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008854	bleb		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0008985	hemimelia		IAGP		N	RGD:5509061	20170209	MGI			PMID:23792766
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009003	abnormal vibrissa number		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009004	progressive hair loss		IAGP		N	RGD:5509061	20170209	MGI			PMID:11748151
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009039	absent inferior colliculus		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009048	enlarged tectum		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009049	abnormal hallux morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009049	abnormal hallux morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6062373
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009569	abnormal left lung morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268579
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009571	abnormal right lung accessory lobe morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268579
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009573	abnormal right lung middle lobe morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268579
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009574	abnormal right lung caudal lobe morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268579
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20180301	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:12112872
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:20386744
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009744	postaxial polydactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:20386744
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009770	abnormal optic chiasm morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18397875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20170209	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0010883	trachea stenosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0010885	absent trachea		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0010906	abnormal lung bud morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:17266131
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:17400206
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:19906844
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:9006072
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:6062373
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:16914490
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:19223390
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:8387379
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:9268579
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011238	abnormal inner ear development		IAGP		N	RGD:5509061	20240822	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22383895
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011362	ectopic adrenal gland		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011505	camptomelia		IAGP		N	RGD:5509061	20170209	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011727	ectopic ovary		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0011964	increased total retina thickness		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0012101	acoria		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0012139	increased forebrain size		IAGP		N	RGD:5509061	20171207	MGI			PMID:20570969
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0012667	split sternal manubrium		IAGP		N	RGD:5509061	20170209	MGI			PMID:7202526
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20170209	MGI			PMID:22383895
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013261	absent epiglottis		IAGP		N	RGD:5509061	20181108	MGI			PMID:11978771
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013362	absent pineal gland		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013362	absent pineal gland		IAGP		N	RGD:5509061	20190228	MGI			PMID:8026071
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013443	Harderian gland hyperplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013496	abnormal trachea development		IAGP		N	RGD:5509061	20170209	MGI			PMID:9731531
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013529	decreased nipple number		IAGP		N	RGD:5509061	20170209	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013720	abnormal mammary line morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16720875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013721	abnormal mammary placode morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16914490
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013785	abnormal mammary gland bud morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16720875
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0013785	abnormal mammary gland bud morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16914490
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:23644062
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0021101	abnormal ventral interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0021101	abnormal ventral interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0021102	abnormal ventral interneuron 0 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0021103	abnormal ventral interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:14723851
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0030031	abnormal forehead morphology		IAGP		N	RGD:5509061	20171123	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0030203	short nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0030205	thick nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:6049666
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0030353	wide sagittal suture		IAGP		N	RGD:5509061	20171207	MGI			PMID:20570969
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0030356	premature lambdoid suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:20570969
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20171214	MGI			PMID:20570969
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0030833	small acromion		IAGP		N	RGD:5509061	20181018	MGI			PMID:15728667
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0031442	enlarged cerebral aqueduct		IAGP		N	RGD:5509061	20221103	MGI			PMID:18480159
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0031447	unilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:5806166
1314554	Gli3	GLI-Kruppel family member GLI3	gene	MP:0031449	abnormal nasal cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:6049666
1314559	Anapc5	anaphase-promoting complex subunit 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0004182	abnormal spermiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314562	Pip5k1a	phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20141003	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20141003	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20150430	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20141003	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0003822	decreased left ventricle systolic pressure		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0004092	absent Z line		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0004093	diffuse Z line		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0004146	absent M line		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0010759	decreased right ventricle systolic pressure		IAGP		N	RGD:5509061	20180503	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0030566	abnormal A band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0030567	abnormal I band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26526197
1314564	Daam2	dishevelled associated activator of morphogenesis 2	gene	MP:0030568	abnormal H zone morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26526197
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0014391	increased hepatocyte mitochondrial DNA content		IAGP		N	RGD:5509061	20240328	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314566	Thrap3	thyroid hormone receptor associated protein 3	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20231012	MGI			PMID:37524868
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000293	absent myocardial trabeculae		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0004387	abnormal prechordal plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0006305	abnormal optic eminence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0008786	abnormal hindgut morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0012155	abnormal optic pit morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0012254	absent intersomitic vessels		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0012510	abnormal aortic sac morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17573777
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0012532	abnormal surface ectoderm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0012702	increased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0012744	increased neural crest cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0012746	abnormal neural crest cell delamination		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314568	Ovol2	ovo like zinc finger 2	gene	MP:0030061	absent otic pit		IAGP		N	RGD:5509061	20200310	MGI			PMID:16423343
1314572	Ly6d	lymphocyte antigen 6 family member D	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20220811	MGI			
1314574	Lsp1	lymphocyte specific 1	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10961883
1314574	Lsp1	lymphocyte specific 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10961883
1314574	Lsp1	lymphocyte specific 1	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11261799
1314574	Lsp1	lymphocyte specific 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10961883
1314574	Lsp1	lymphocyte specific 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11261799
1314574	Lsp1	lymphocyte specific 1	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15684321
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314576	Smarcal1	SNF2 related chromatin remodeling ATPase like 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378147
1314580	Acsf3	acyl-CoA synthetase family member 3	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20230601	MGI			
1314585	Tdrd1	tudor domain containing 1	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1314585	Tdrd1	tudor domain containing 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1314585	Tdrd1	tudor domain containing 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1314585	Tdrd1	tudor domain containing 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1314585	Tdrd1	tudor domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1314585	Tdrd1	tudor domain containing 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1314585	Tdrd1	tudor domain containing 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1314585	Tdrd1	tudor domain containing 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1314585	Tdrd1	tudor domain containing 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:17038506
1314585	Tdrd1	tudor domain containing 1	gene	MP:0031620	abnormal chromatoid body morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:17038506
1314587	Evpl	envoplakin	gene	MP:0009594	abnormal corneocyte envelope morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564887
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20210121	MGI			PMID:32987832
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20190912	MGI			PMID:30335140
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20190912	MGI			PMID:30335140
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20190613	MGI			PMID:30602030
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20190912	MGI			PMID:30335140
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20190912	MGI			PMID:30335140
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:30335140
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20190912	MGI			PMID:30335140
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190613	MGI			PMID:30602030
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210121	MGI			PMID:32987832
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190613	MGI			PMID:30602030
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210121	MGI			PMID:32987832
1314590	Tbc1d24	TBC1 domain family, member 24	gene	MP:0030951	abnormal endocytosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:30335140
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0002338	abnormal pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509100
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878307
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:18509100
1314595	Pask	PAS domain containing serine/threonine kinase	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:17878307
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31910261
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20200213	MGI			PMID:31910261
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20200213	MGI			PMID:31910261
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0010733	abnormal axon initial segment morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31910261
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31910261
1314599	Ecpas	Ecm29 proteasome adaptor and scaffold	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210520	MGI			
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733590
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0002234	abnormal pharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0004555	pharynx hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20220519	MGI			
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314600	Nkx2-6	NK2 homeobox 6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390666
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20231207	MGI			
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20240523	MGI			
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0010360	decreased liver free fatty acids level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0012230	abnormal sphingolipid level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0012338	decreased bile salt level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0014448	increased enzyme/coenzyme level		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314602	Atp10a	ATPase, class V, type 10A	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20250605	MGI			PMID:38172157
1314603	Fam234b	family with sequence similarity 234, member B	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1314603	Fam234b	family with sequence similarity 234, member B	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20160804	MGI			
1314603	Fam234b	family with sequence similarity 234, member B	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1314603	Fam234b	family with sequence similarity 234, member B	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1314603	Fam234b	family with sequence similarity 234, member B	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1314603	Fam234b	family with sequence similarity 234, member B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20160804	MGI			
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0011579	decreased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0014740	increased auditory brainstem response wave peak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:23297193
1314605	Abhd12	abhydrolase domain containing 12	gene	MP:0014742	increased auditory brainstem response wave interpeak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:23297193
1314606	Tmem231	transmembrane protein 231	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1314606	Tmem231	transmembrane protein 231	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1314606	Tmem231	transmembrane protein 231	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1314606	Tmem231	transmembrane protein 231	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1314606	Tmem231	transmembrane protein 231	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1314606	Tmem231	transmembrane protein 231	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179047
1314608	Copz1	coatomer protein complex, subunit zeta 1	gene	MP:0009455	enhanced cued conditioning behavior		IEA		N	RGD:5509061	20260402	MGI			
1314608	Copz1	coatomer protein complex, subunit zeta 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1314608	Copz1	coatomer protein complex, subunit zeta 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20260402	MGI			
1314609	Radil	Ras association and DIL domains	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1314609	Radil	Ras association and DIL domains	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180189
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10848582
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0009442	increased ovarian teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10848582
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180189
1314611	Dclre1a	DNA cross-link repair 1A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260620
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20220929	MGI			PMID:36028484
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20220929	MGI			PMID:36028484
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20220929	MGI			PMID:36028484
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0014379	decreased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314612	Prmt9	protein arginine methyltransferase 9	gene	MP:0021088	impaired spatial memory extinction		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1314614	Hoxb9	homeobox B9	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1314614	Hoxb9	homeobox B9	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1314614	Hoxb9	homeobox B9	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892669
1314614	Hoxb9	homeobox B9	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1314614	Hoxb9	homeobox B9	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892669
1314614	Hoxb9	homeobox B9	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1314614	Hoxb9	homeobox B9	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0003344	mammary gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892669
1314614	Hoxb9	homeobox B9	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1314614	Hoxb9	homeobox B9	gene	MP:0004323	sternum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1314614	Hoxb9	homeobox B9	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1314614	Hoxb9	homeobox B9	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1314614	Hoxb9	homeobox B9	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314614	Hoxb9	homeobox B9	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20160811	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20160811	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1314616	Atp6v0d1	ATPase, H+ transporting, lysosomal V0 subunit D1	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38505620
1314618	Lrp1b	low density lipoprotein-related protein 1B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082773
1314618	Lrp1b	low density lipoprotein-related protein 1B	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1314618	Lrp1b	low density lipoprotein-related protein 1B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383322
1314618	Lrp1b	low density lipoprotein-related protein 1B	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383322
1314618	Lrp1b	low density lipoprotein-related protein 1B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1314618	Lrp1b	low density lipoprotein-related protein 1B	gene	MP:0011897	decreased circulating unsaturated transferrin level		IEA		N	RGD:5509061	20260402	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20111116	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210128	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0001846	increased inflammatory response		IEA		N	RGD:5509061	20111116	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20201022	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0002461	increased immunoglobulin level		IEA		N	RGD:5509061	20111116	MGI			
1314620	Fkbp11	FK506 binding protein 11	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20111116	MGI			
1314624	Ephb6	Eph receptor B6	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540454
1314624	Ephb6	Eph receptor B6	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540454
1314624	Ephb6	Eph receptor B6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379224
1314624	Ephb6	Eph receptor B6	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540454
1314624	Ephb6	Eph receptor B6	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15599401
1314624	Ephb6	Eph receptor B6	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15599401
1314624	Ephb6	Eph receptor B6	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540454
1314624	Ephb6	Eph receptor B6	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15599401
1314624	Ephb6	Eph receptor B6	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15599401
1314624	Ephb6	Eph receptor B6	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540454
1314624	Ephb6	Eph receptor B6	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540454
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20200514	MGI			
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30605677
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30605677
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20191024	MGI			PMID:30605677
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20200514	MGI			
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230601	MGI			
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20240530	MGI			PMID:36097267
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30605677
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20200514	MGI			
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20190516	MGI			PMID:20178993
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:36097267
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20211021	MGI			
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190516	MGI			PMID:20178993
1314628	Zdhhc5	zinc finger, DHHC domain containing 5	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111477
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111477
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532117
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532117
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20111116	MGI			
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532117
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:28593200
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:28593200
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111477
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532117
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20180517	MGI			PMID:29242247
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532117
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20180517	MGI			PMID:29242247
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20180517	MGI			PMID:29242247
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20180517	MGI			PMID:28593200
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532117
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532117
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111477
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532117
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20180517	MGI			PMID:29242247
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0011466	increased urine urea nitrogen level		IAGP		N	RGD:5509061	20180517	MGI			PMID:29242247
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0011470	increased urine creatinine level		IAGP		N	RGD:5509061	20180517	MGI			PMID:29242247
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20180517	MGI			PMID:29242247
1314630	Stub1	STIP1 homology and U-Box containing protein 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113144
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230119	MGI			
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230119	MGI			
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20230119	MGI			
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230119	MGI			
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230119	MGI			
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180222	MGI			PMID:26051944
1314632	Inpp5a	inositol polyphosphate-5-phosphatase A	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20230119	MGI			
1314634	Exosc8	exosome component 8	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20240523	MGI			
1314634	Exosc8	exosome component 8	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1314634	Exosc8	exosome component 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314634	Exosc8	exosome component 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1314634	Exosc8	exosome component 8	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200827	MGI			PMID:25975270
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20181227	MGI			
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0001192	scaly skin		IEA		N	RGD:5509061	20181227	MGI			
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20200827	MGI			PMID:25975270
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002293	long gestation period		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200827	MGI			PMID:25975270
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002681	increased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200827	MGI			PMID:25975270
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20200827	MGI			PMID:25975270
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0004832	enlarged ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200827	MGI			PMID:25975270
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200827	MGI			PMID:25975270
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20200827	MGI			PMID:25975270
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20200827	MGI			PMID:25975270
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:19056881
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
1314637	Tiparp	TCDD-inducible poly(ADP-ribose) polymerase	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:17143286
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376969
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376969
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376969
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376969
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23142661
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376969
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376969
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376969
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0014382	increased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:22710612
1314643	Lhx6	LIM homeobox protein 6	gene	MP:0014553	decreased neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:17376969
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0001841	decreased level of surface class I molecules		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0010539	decreased level of surface class II molecules		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314647	Arfgap2	ARF GTPase activating protein 2	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1314653	Leng8	leukocyte receptor cluster (LRC) member 8	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20260402	MGI			
1314653	Leng8	leukocyte receptor cluster (LRC) member 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1314654	Tmem150b	transmembrane protein 150B	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20200514	MGI			
1314654	Tmem150b	transmembrane protein 150B	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20210520	MGI			
1314654	Tmem150b	transmembrane protein 150B	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201022	MGI			
1314654	Tmem150b	transmembrane protein 150B	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1314654	Tmem150b	transmembrane protein 150B	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20200514	MGI			
1314654	Tmem150b	transmembrane protein 150B	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1314654	Tmem150b	transmembrane protein 150B	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20200514	MGI			
1314654	Tmem150b	transmembrane protein 150B	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20210520	MGI			
1314654	Tmem150b	transmembrane protein 150B	gene	MP:0013522	decreased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20210520	MGI			
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0004371	bowed femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0004372	bowed fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0004373	bowed humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0008274	failure of bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:20684022
1314656	Phospho1	phosphatase, orphan 1	gene	MP:0021184	decreased bone mineral density of humerus		IAGP		N	RGD:5509061	20220915	MGI			PMID:20684022
1314661	Pramel13	PRAME like 13	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1314661	Pramel13	PRAME like 13	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20210805	MGI			PMID:31729367
1314661	Pramel13	PRAME like 13	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
1314661	Pramel13	PRAME like 13	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210805	MGI			PMID:31729367
1314661	Pramel13	PRAME like 13	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1314661	Pramel13	PRAME like 13	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20210805	MGI			PMID:31729367
1314661	Pramel13	PRAME like 13	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
1314661	Pramel13	PRAME like 13	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1314661	Pramel13	PRAME like 13	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20210805	MGI			PMID:31729367
1314661	Pramel13	PRAME like 13	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20210805	MGI			PMID:31729367
1314661	Pramel13	PRAME like 13	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20210805	MGI			PMID:31729367
1314661	Pramel13	PRAME like 13	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20210805	MGI			PMID:31729367
1314663	Ivl	involucrin	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20210128	MGI			
1314663	Ivl	involucrin	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1314663	Ivl	involucrin	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210128	MGI			
1314663	Ivl	involucrin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11038184
1314663	Ivl	involucrin	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20150430	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20141003	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20160114	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20170105	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20150430	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20141003	MGI			
1314667	Wdr37	WD repeat domain 37	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20150108	MGI			
1314675	Eif5a2	eukaryotic translation initiation factor 5A2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170706	MGI			PMID:26037925
1314682	Lrch3	leucine-rich repeats and calponin homology (CH) domain containing 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20250508	MGI			
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0010174	decreased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20191128	MGI			
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0012075	impaired mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314684	Igfbp7	insulin-like growth factor binding protein 7	gene	MP:0013782	abnormal mammary duct terminal end bud morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:24505323
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0005044	sepsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20160225	MGI			PMID:25180606
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314688	Serpinb1a	serine (or cysteine) peptidase inhibitor, clade B, member 1a	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664292
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:17496142
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160204	MGI			PMID:17496142
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20160204	MGI			PMID:17496142
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160204	MGI			PMID:17496142
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20160204	MGI			PMID:17496142
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20160204	MGI			PMID:17496142
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20160204	MGI			PMID:17496142
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20160204	MGI			PMID:17496142
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20160204	MGI			PMID:17496142
1314690	Pde6d	phosphodiesterase 6D, cGMP-specific, rod, delta	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:17496142
1314692	Fzd7	frizzled class receptor 7	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314692	Fzd7	frizzled class receptor 7	gene	MP:0011203	abnormal parietal yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1314693	Kif21b	kinesin family member 21B	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1314693	Kif21b	kinesin family member 21B	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160804	MGI			
1314693	Kif21b	kinesin family member 21B	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1314693	Kif21b	kinesin family member 21B	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1314693	Kif21b	kinesin family member 21B	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:27117409
1314693	Kif21b	kinesin family member 21B	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20180125	MGI			PMID:27117409
1314693	Kif21b	kinesin family member 21B	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:27117409
1314693	Kif21b	kinesin family member 21B	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20180125	MGI			PMID:27117409
1314693	Kif21b	kinesin family member 21B	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:27117409
1314693	Kif21b	kinesin family member 21B	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20180125	MGI			PMID:27117409
1314696	Lkaaear1	LKAAEAR motif containing 1 (IKAAEAR murine motif)	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20241121	MGI			
1314697	Zfp746	zinc finger protein 746	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220519	MGI			
1314697	Zfp746	zinc finger protein 746	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1314697	Zfp746	zinc finger protein 746	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1314697	Zfp746	zinc finger protein 746	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1314697	Zfp746	zinc finger protein 746	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1314697	Zfp746	zinc finger protein 746	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1314697	Zfp746	zinc finger protein 746	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20240523	MGI			
1314697	Zfp746	zinc finger protein 746	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1314697	Zfp746	zinc finger protein 746	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240314	MGI			PMID:34062393
1314697	Zfp746	zinc finger protein 746	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1314697	Zfp746	zinc finger protein 746	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1314699	Spin1	spindlin 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1314699	Spin1	spindlin 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1314699	Spin1	spindlin 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1314699	Spin1	spindlin 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1314699	Spin1	spindlin 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1314699	Spin1	spindlin 1	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0004094	abnormal M line morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20181227	MGI			
1314699	Spin1	spindlin 1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0010767	abnormal female meiosis I arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23894536
1314699	Spin1	spindlin 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23894536
1314699	Spin1	spindlin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1314699	Spin1	spindlin 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000192	abnormal mineral level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:7579418
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20201022	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000414	alopecia		IEA		N	RGD:5509061	20111116	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1325193
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000472	abnormal stomach non-glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1325193
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7650236
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000580	deformed nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:7650236
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7579418
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7579418
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7579418
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7579418
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001195	flaky skin		IEA		N	RGD:5509061	20111116	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001212	skin lesions		IEA		N	RGD:5509061	20111116	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7650236
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7650236
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20171012	MGI			PMID:8406628
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001220	epidermal necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IEA		N	RGD:5509061	20111116	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001243	abnormal dermal layer morphology		IEA		N	RGD:5509061	20111116	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7579418
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1325193
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001586	abnormal erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001586	abnormal erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1325193
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:1325193
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7650236
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7650236
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20170921	MGI			PMID:7650236
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0004152	abnormal circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0005096	erythroblastosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0005096	erythroblastosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0005174	abnormal tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155459
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0009600	hypergranulosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7650236
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0009602	abnormal keratohyalin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7650236
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0009675	orthokeratosis		IEA		N	RGD:5509061	20111116	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20200402	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0010176	dacryocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0010177	acanthocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0010784	abnormal forestomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1325193
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1325193
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0011242	increased fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093647
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0011413	colorless urine		IAGP		N	RGD:5509061	20141003	MGI			PMID:6678340
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0013409	increased dendritic epidermal T cell number		IAGP		N	RGD:5509061	20171012	MGI			PMID:8406628
1314701	Ttc7	tetratricopeptide repeat domain 7	gene	MP:0013412	increased Langerhans cell number		IAGP		N	RGD:5509061	20171012	MGI			PMID:8406628
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20250508	MGI			
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0002798	abnormal active avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1314704	Pak6	p21 (RAC1) activated kinase 6	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20201231	MGI			
1314705	Csrnp3	cysteine-serine-rich nuclear protein 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17726538
1314705	Csrnp3	cysteine-serine-rich nuclear protein 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17726538
1314706	Paxx	non-homologous end joining factor	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1314706	Paxx	non-homologous end joining factor	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0000726	absent lymphocyte		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1314706	Paxx	non-homologous end joining factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1314706	Paxx	non-homologous end joining factor	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20170413	MGI			PMID:27798842
1314706	Paxx	non-homologous end joining factor	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20240523	MGI			
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20141003	MGI			
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693278
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693278
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693278
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693278
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0004113	abnormal aortic arch morphology		IEA		N	RGD:5509061	20141003	MGI			
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693278
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464436
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0011659	interrupted aortic arch, type b		IEA		N	RGD:5509061	20231214	MGI			
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0011662	persistent truncus arteriosus type ii		IEA		N	RGD:5509061	20231228	MGI			
1314708	Tab1	TGF-beta activated kinase 1/MAP3K7 binding protein 1	gene	MP:0011676	aortic arch obstruction		IEA		N	RGD:5509061	20231228	MGI			
1314710	Pcp2	Purkinje cell protein 2 (L7)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270300
1314710	Pcp2	Purkinje cell protein 2 (L7)	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270300
1314710	Pcp2	Purkinje cell protein 2 (L7)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883005
1314710	Pcp2	Purkinje cell protein 2 (L7)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9191112
1314710	Pcp2	Purkinje cell protein 2 (L7)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9204480
1314710	Pcp2	Purkinje cell protein 2 (L7)	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17270300
1314718	Aqr	aquarius	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1314718	Aqr	aquarius	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643689
1314718	Aqr	aquarius	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626505
1314720	Gtsf1l	gametocyte specific factor 1-like	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1314722	Tprg1	transformation related protein 63 regulated 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20231207	MGI			
1314722	Tprg1	transformation related protein 63 regulated 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20231207	MGI			
1314722	Tprg1	transformation related protein 63 regulated 1	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20231207	MGI			
1314722	Tprg1	transformation related protein 63 regulated 1	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20231207	MGI			
1314722	Tprg1	transformation related protein 63 regulated 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1314723	4833420G17Rik	RIKEN cDNA 4833420G17 gene	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20230601	MGI			
1314723	4833420G17Rik	RIKEN cDNA 4833420G17 gene	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1314723	4833420G17Rik	RIKEN cDNA 4833420G17 gene	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20241121	MGI			
1314726	Setbp1	SET binding protein 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20210826	MGI			
1314726	Setbp1	SET binding protein 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1314726	Setbp1	SET binding protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20171109	MGI			PMID:26496356
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20171109	MGI			PMID:26496356
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20171109	MGI			PMID:26496356
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20171109	MGI			PMID:26496356
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0008261	arrest of male meiosis		IEA		N	RGD:5509061	20220721	MGI			
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26496356
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0009236	pinhead sperm		IAGP		N	RGD:5509061	20171109	MGI			PMID:26496356
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20171109	MGI			PMID:26496356
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26496356
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20171109	MGI			PMID:26496356
1314727	Henmt1	HEN1 methyltransferase homolog 1 (Arabidopsis)	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:26496356
1314729	Rwdd2a	RWD domain containing 2A	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230105	MGI			
1314729	Rwdd2a	RWD domain containing 2A	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20230105	MGI			
1314729	Rwdd2a	RWD domain containing 2A	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1314729	Rwdd2a	RWD domain containing 2A	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230105	MGI			
1314729	Rwdd2a	RWD domain containing 2A	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1314729	Rwdd2a	RWD domain containing 2A	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230105	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0000650	mesocardia		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20220120	MGI			PMID:34715025
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170504	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20220120	MGI			PMID:34715025
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20220120	MGI			PMID:34715025
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0008933	abnormal motile primary cilium physiology		IAGP		N	RGD:5509061	20220120	MGI			PMID:34715025
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0008987	abnormal liver lobule morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20230720	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0010595	abnormal aortic valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0010853	abnormal lung position or orientation		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0010975	abnormal lung lobe morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20220120	MGI			PMID:34715025
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220120	MGI			PMID:34715025
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220120	MGI			PMID:34715025
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0013847	retropleural edema		IEA		N	RGD:5509061	20170504	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1314732	Pierce1	piercer of microtubule wall 1	gene	MP:0020494	left sided inferior vena cava		IAGP		N	RGD:5509061	20180222	MGI			PMID:27305836
1314739	Kctd7	potassium channel tetramerisation domain containing 7	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20190711	MGI			
1314739	Kctd7	potassium channel tetramerisation domain containing 7	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1314739	Kctd7	potassium channel tetramerisation domain containing 7	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1314739	Kctd7	potassium channel tetramerisation domain containing 7	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1314760	Krt33a	keratin 33A	gene	MP:0000411	shiny fur		IEA		N	RGD:5509061	20111116	MGI			
1314760	Krt33a	keratin 33A	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1314760	Krt33a	keratin 33A	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1314760	Krt33a	keratin 33A	gene	MP:0001511	disheveled coat		IEA		N	RGD:5509061	20111116	MGI			
1314760	Krt33a	keratin 33A	gene	MP:0003849	greasy coat		IEA		N	RGD:5509061	20111116	MGI			
1314760	Krt33a	keratin 33A	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20211021	MGI			
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20240523	MGI			
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1314764	Elavl2	ELAV like RNA binding protein 2	gene	MP:0011122	absent primordial ovarian follicles		IAGP		N	RGD:5509061	20230928	MGI			PMID:31657143
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20201022	MGI			
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20201022	MGI			
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0009597	impaired stratum corneum desquamation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22832496
1314766	Aloxe3	arachidonate lipoxygenase 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20250710	MGI			PMID:40472089
1314768	Gpr45	G protein-coupled receptor 45	gene	MP:0014638	increased sleep duration		IAGP		N	RGD:5509061	20250703	MGI			PMID:27500489
1314770	Ap2a1	adaptor-related protein complex 2, alpha 1 subunit	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1314770	Ap2a1	adaptor-related protein complex 2, alpha 1 subunit	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1314770	Ap2a1	adaptor-related protein complex 2, alpha 1 subunit	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1314770	Ap2a1	adaptor-related protein complex 2, alpha 1 subunit	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1314770	Ap2a1	adaptor-related protein complex 2, alpha 1 subunit	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
1314770	Ap2a1	adaptor-related protein complex 2, alpha 1 subunit	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1314770	Ap2a1	adaptor-related protein complex 2, alpha 1 subunit	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20250918	MGI			PMID:38407237
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20250918	MGI			PMID:38407237
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0001785	edema		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20250918	MGI			PMID:38407237
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0005380	embryo phenotype		IAGP		N	RGD:5509061	20250918	MGI			PMID:38407237
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20250918	MGI			PMID:38407237
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20241121	MGI			
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20250918	MGI			PMID:38407237
1314771	Sass6	SAS-6 centriolar assembly protein	gene	MP:0031682	abnormal centriole morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:38407237
1314776	Clca1	chloride channel accessory 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645179
1314776	Clca1	chloride channel accessory 1	gene	MP:0001102	small superior vagus ganglion		IEA		N	RGD:5509061	20181227	MGI			
1314776	Clca1	chloride channel accessory 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15947424
1314776	Clca1	chloride channel accessory 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645179
1314776	Clca1	chloride channel accessory 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645179
1314776	Clca1	chloride channel accessory 1	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20210128	MGI			
1314776	Clca1	chloride channel accessory 1	gene	MP:0002281	abnormal respiratory mucosa goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645179
1314776	Clca1	chloride channel accessory 1	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645179
1314776	Clca1	chloride channel accessory 1	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645179
1314776	Clca1	chloride channel accessory 1	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20181227	MGI			
1314776	Clca1	chloride channel accessory 1	gene	MP:0010936	decreased airway resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645179
1314781	Btbd7	BTB domain containing 7	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20250508	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20181227	MGI			PMID:28506999
1314781	Btbd7	BTB domain containing 7	gene	MP:0009520	decreased submandibular gland size		IAGP		N	RGD:5509061	20181227	MGI			PMID:28506999
1314781	Btbd7	BTB domain containing 7	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20181227	MGI			PMID:28506999
1314781	Btbd7	BTB domain containing 7	gene	MP:0010895	increased lung compliance		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20181227	MGI			PMID:28506999
1314781	Btbd7	BTB domain containing 7	gene	MP:0011045	decreased lung elastance		IEA		N	RGD:5509061	20230119	MGI			
1314781	Btbd7	BTB domain containing 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20181227	MGI			PMID:28506999
1314781	Btbd7	BTB domain containing 7	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20181227	MGI			PMID:28506999
1314781	Btbd7	BTB domain containing 7	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20181227	MGI			PMID:28506999
1314781	Btbd7	BTB domain containing 7	gene	MP:0013541	abnormal submandibular gland development		IAGP		N	RGD:5509061	20181227	MGI			PMID:28506999
1314781	Btbd7	BTB domain containing 7	gene	MP:0013542	abnormal submandibular gland branching morphogenesis		IAGP		N	RGD:5509061	20181227	MGI			PMID:28506999
1314783	Slamf8	SLAM family member 8	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593622
1314783	Slamf8	SLAM family member 8	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22593622
1314785	Zfp763	zinc finger protein 763	gene	MP:0003443	increased circulating glycerol level		IEA		N	RGD:5509061	20211021	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20230119	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230119	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20230119	MGI			
1314787	Capza1	capping actin protein of muscle Z-line subunit alpha 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1314793	Sipa1l2	signal-induced proliferation-associated 1 like 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200730	MGI			PMID:31784514
1314793	Sipa1l2	signal-induced proliferation-associated 1 like 2	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20200730	MGI			PMID:31784514
1314794	Acad11	acyl-Coenzyme A dehydrogenase family, member 11	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1314794	Acad11	acyl-Coenzyme A dehydrogenase family, member 11	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1314794	Acad11	acyl-Coenzyme A dehydrogenase family, member 11	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1314795	D630045J12Rik	RIKEN cDNA D630045J12 gene	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1314795	D630045J12Rik	RIKEN cDNA D630045J12 gene	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1314795	D630045J12Rik	RIKEN cDNA D630045J12 gene	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1314795	D630045J12Rik	RIKEN cDNA D630045J12 gene	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20170105	MGI			
1314795	D630045J12Rik	RIKEN cDNA D630045J12 gene	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20190502	MGI			
1314795	D630045J12Rik	RIKEN cDNA D630045J12 gene	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1314795	D630045J12Rik	RIKEN cDNA D630045J12 gene	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1314795	D630045J12Rik	RIKEN cDNA D630045J12 gene	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1314797	Spic	Spi-C transcription factor (Spi-1/PU.1 related)	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037245
1314797	Spic	Spi-C transcription factor (Spi-1/PU.1 related)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24630724
1314797	Spic	Spi-C transcription factor (Spi-1/PU.1 related)	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037245
1314797	Spic	Spi-C transcription factor (Spi-1/PU.1 related)	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24630724
1314797	Spic	Spi-C transcription factor (Spi-1/PU.1 related)	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037245
1314797	Spic	Spi-C transcription factor (Spi-1/PU.1 related)	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037245
1314797	Spic	Spi-C transcription factor (Spi-1/PU.1 related)	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037245
1314799	Fer	FER tyrosine kinase	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201022	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220519	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134346
1314799	Fer	FER tyrosine kinase	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20220519	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1314799	Fer	FER tyrosine kinase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201022	MGI			
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148091
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148091
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148091
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148091
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148091
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148091
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:26683084
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20190110	MGI			
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0008170	decreased B-1b cell number		IEA		N	RGD:5509061	20190110	MGI			
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148091
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148091
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0008191	abnormal follicular B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148091
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0009938	abnormal hippocampus granule cell morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:26683084
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20171116	MGI			PMID:26683084
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0020335	abnormal dentate gyrus neuron dendrite morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:26683084
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20211014	MGI			PMID:26683084
1314804	Nedd9	neural precursor cell expressed, developmentally down-regulated gene 9	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
1314807	Zfp282	zinc finger protein 282	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1314807	Zfp282	zinc finger protein 282	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
1314807	Zfp282	zinc finger protein 282	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240822	MGI			PMID:38050179
1314809	Abr	active BCR-related gene	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0003143	enlarged otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0003144	decreased otolith number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11921339
1314809	Abr	active BCR-related gene	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684658
1314809	Abr	active BCR-related gene	gene	MP:0011238	abnormal inner ear development		IAGP		N	RGD:5509061	20240822	MGI			PMID:11921339
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0001717	absent ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20170216	MGI			PMID:27068806
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27068806
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20170216	MGI			PMID:27068806
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20170216	MGI			PMID:27068806
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20170216	MGI			PMID:27068806
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0010040	abnormal oval cell morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27068806
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0010042	abnormal oval cell physiology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27068806
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0011197	abnormal proamniotic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0011198	absent proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0011208	small proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199142
1314811	Ppp1r8	protein phosphatase 1, regulatory subunit 8	gene	MP:0014233	bile duct epithelium hyperplasia		IAGP		N	RGD:5509061	20170216	MGI			PMID:27068806
1314813	Aamp	angio-associated migratory protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1314813	Aamp	angio-associated migratory protein	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20220811	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20260402	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0004156	abnormal QT variability		IEA		N	RGD:5509061	20260402	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20160804	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160804	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20260402	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314816	Ndufa8	NADH:ubiquinone oxidoreductase subunit A8	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20160421	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20221215	MGI			PMID:36099048
1314817	Mettl23	methyltransferase like 23	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20230316	MGI			PMID:28930672
1314817	Mettl23	methyltransferase like 23	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0002981	increased liver weight		IEA		N	RGD:5509061	20260402	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20260402	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20221215	MGI			PMID:36099048
1314817	Mettl23	methyltransferase like 23	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20260402	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20260402	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0005391	vision/eye phenotype		IAGP		N	RGD:5509061	20221215	MGI			PMID:36099048
1314817	Mettl23	methyltransferase like 23	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20221215	MGI			PMID:36099048
1314817	Mettl23	methyltransferase like 23	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20221215	MGI			PMID:36099048
1314817	Mettl23	methyltransferase like 23	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20230316	MGI			PMID:28930672
1314817	Mettl23	methyltransferase like 23	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20230316	MGI			PMID:28930672
1314817	Mettl23	methyltransferase like 23	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230316	MGI			PMID:28930672
1314817	Mettl23	methyltransferase like 23	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20260402	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20230601	MGI			
1314817	Mettl23	methyltransferase like 23	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139088
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139088
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15848800
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139088
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158234
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158234
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15848800
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0003184	increased angiotensin I-converting enzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782872
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782872
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005489	vascular smooth muscle hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005497	optic nerve cupping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782872
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005610	increased circulating antidiuretic hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005662	increased circulating adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0005665	increased circulating noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008300	enlarged adrenal medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008301	adrenal medulla hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158234
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158234
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:11376343
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0009812	abnormal bradykinin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22683124
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20150430	MGI			PMID:20140222
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:11376342
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:14623913
1314819	Vav2	vav guanine nucleotide exchange factor 2	gene	MP:0014697	abnormal fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:16782872
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20190404	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001394	circling		IEA		N	RGD:5509061	20190404	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0009122	decreased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0009974	decreased cerebral cortex pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0011975	neuronal cytoplasmic inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479740
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20210826	MGI			
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0020811	abnormal photoreceptor outer segment size		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314820	Epg5	ectopic P-granules 5 autophagy tethering factor	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200206	MGI			PMID:27715390
1314821	Zfc3h1	zinc finger, C3H1-type containing	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220811	MGI			
1314821	Zfc3h1	zinc finger, C3H1-type containing	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20220811	MGI			
1314821	Zfc3h1	zinc finger, C3H1-type containing	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1314821	Zfc3h1	zinc finger, C3H1-type containing	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20231207	MGI			
1314821	Zfc3h1	zinc finger, C3H1-type containing	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1314821	Zfc3h1	zinc finger, C3H1-type containing	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1314823	Plpp4	phospholipid phosphatase 4	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1314825	Ivns1abp	influenza virus NS1A binding protein	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485691
1314825	Ivns1abp	influenza virus NS1A binding protein	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485691
1314825	Ivns1abp	influenza virus NS1A binding protein	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485691
1314825	Ivns1abp	influenza virus NS1A binding protein	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485691
1314825	Ivns1abp	influenza virus NS1A binding protein	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485691
1314825	Ivns1abp	influenza virus NS1A binding protein	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485691
1314825	Ivns1abp	influenza virus NS1A binding protein	gene	MP:0010334	pleural effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485691
1314825	Ivns1abp	influenza virus NS1A binding protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485691
1314827	Slc39a2	solute carrier family 39 (zinc transporter), member 2	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17506078
1314827	Slc39a2	solute carrier family 39 (zinc transporter), member 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17506078
1314827	Slc39a2	solute carrier family 39 (zinc transporter), member 2	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17506078
1314827	Slc39a2	solute carrier family 39 (zinc transporter), member 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17506078
1314827	Slc39a2	solute carrier family 39 (zinc transporter), member 2	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17506078
1314827	Slc39a2	solute carrier family 39 (zinc transporter), member 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17506078
1314827	Slc39a2	solute carrier family 39 (zinc transporter), member 2	gene	MP:0008738	abnormal liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17506078
1314829	Trdmt1	tRNA aspartic acid methyltransferase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1314829	Trdmt1	tRNA aspartic acid methyltransferase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1314829	Trdmt1	tRNA aspartic acid methyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16424344
1314829	Trdmt1	tRNA aspartic acid methyltransferase 1	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20111116	MGI			
1314829	Trdmt1	tRNA aspartic acid methyltransferase 1	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1314829	Trdmt1	tRNA aspartic acid methyltransferase 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1314829	Trdmt1	tRNA aspartic acid methyltransferase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1314831	Skil	SKI-like proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861029
1314831	Skil	SKI-like proto-oncogene	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861029
1314831	Skil	SKI-like proto-oncogene	gene	MP:0001881	abnormal mammary gland physiology		IAGP		N	RGD:5509061	20161208	MGI			PMID:22833129
1314831	Skil	SKI-like proto-oncogene	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811619
1314831	Skil	SKI-like proto-oncogene	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811619
1314831	Skil	SKI-like proto-oncogene	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861029
1314831	Skil	SKI-like proto-oncogene	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811619
1314831	Skil	SKI-like proto-oncogene	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19745809
1314831	Skil	SKI-like proto-oncogene	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811619
1314831	Skil	SKI-like proto-oncogene	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19745809
1314831	Skil	SKI-like proto-oncogene	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861029
1314831	Skil	SKI-like proto-oncogene	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811619
1314831	Skil	SKI-like proto-oncogene	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20161208	MGI			PMID:22833129
1314831	Skil	SKI-like proto-oncogene	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19745809
1314831	Skil	SKI-like proto-oncogene	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20161208	MGI			PMID:22833129
1314831	Skil	SKI-like proto-oncogene	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20161208	MGI			PMID:22833129
1314831	Skil	SKI-like proto-oncogene	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811619
1314831	Skil	SKI-like proto-oncogene	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20221215	MGI			
1314831	Skil	SKI-like proto-oncogene	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811619
1314831	Skil	SKI-like proto-oncogene	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19745809
1314831	Skil	SKI-like proto-oncogene	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19745809
1314831	Skil	SKI-like proto-oncogene	gene	MP:0012075	impaired mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20161208	MGI			PMID:22833129
1314831	Skil	SKI-like proto-oncogene	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20161208	MGI			PMID:22833129
1314831	Skil	SKI-like proto-oncogene	gene	MP:0013781	abnormal mammary gland luminal epithelium morphology		IAGP		N	RGD:5509061	20161208	MGI			PMID:22833129
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675108
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675108
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:31549961
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0001055	failure of neuromuscular synapse postsynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675108
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200220	MGI			PMID:31549961
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675108
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20200220	MGI			PMID:31549961
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:31549961
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200220	MGI			PMID:31549961
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675108
1314836	Rapsn	receptor-associated protein of the synapse	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314838	Pcdh20	protocadherin 20	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1314838	Pcdh20	protocadherin 20	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20200514	MGI			
1314838	Pcdh20	protocadherin 20	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1314838	Pcdh20	protocadherin 20	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1314842	Ipp	IAP promoted placental gene	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1314842	Ipp	IAP promoted placental gene	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20181227	MGI			
1314842	Ipp	IAP promoted placental gene	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1314842	Ipp	IAP promoted placental gene	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20220811	MGI			
1314842	Ipp	IAP promoted placental gene	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1314842	Ipp	IAP promoted placental gene	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20211021	MGI			
1314843	Eef1akmt2	EEF1A lysine methyltransferase 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201022	MGI			
1314843	Eef1akmt2	EEF1A lysine methyltransferase 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1314843	Eef1akmt2	EEF1A lysine methyltransferase 2	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20201022	MGI			
1314847	Adam21	a disintegrin and metallopeptidase domain 21	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:34631320
1314848	Tmem203	transmembrane protein 203	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20181227	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25996873
1314848	Tmem203	transmembrane protein 203	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20160602	MGI			PMID:25996873
1314848	Tmem203	transmembrane protein 203	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160602	MGI			PMID:25996873
1314848	Tmem203	transmembrane protein 203	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20160602	MGI			PMID:25996873
1314848	Tmem203	transmembrane protein 203	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160602	MGI			PMID:25996873
1314848	Tmem203	transmembrane protein 203	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0004182	abnormal spermiation		IAGP		N	RGD:5509061	20160602	MGI			PMID:25996873
1314848	Tmem203	transmembrane protein 203	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20160602	MGI			PMID:25996873
1314848	Tmem203	transmembrane protein 203	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20160602	MGI			PMID:25996873
1314848	Tmem203	transmembrane protein 203	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25996873
1314848	Tmem203	transmembrane protein 203	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1314848	Tmem203	transmembrane protein 203	gene	MP:0020352	abnormal endoplasmic reticulum physiology		IAGP		N	RGD:5509061	20161013	MGI			PMID:25996873
1314850	Tjp1	tight junction protein 1	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23977053
1314850	Tjp1	tight junction protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0003891	increased allantois apoptosis		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0004557	dilated allantois		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0008991	abnormal bile canaliculus morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0009501	abnormal hepatic duct morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0011304	kidney papillary atrophy		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0011534	granular kidney		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0011855	abnormal glomerular filtration barrier morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0011869	detached podocyte		IAGP		N	RGD:5509061	20160602	MGI			PMID:25184792
1314850	Tjp1	tight junction protein 1	gene	MP:0012246	abnormal hepatic cord morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:33184034
1314850	Tjp1	tight junction protein 1	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314850	Tjp1	tight junction protein 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20151203	MGI			PMID:18353970
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2726749
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465590
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3678603
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7891151
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465590
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:2726749
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:2077109
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:3678603
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824473
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001017	abnormal stellate ganglion morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20181011	MGI			PMID:27831556
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465590
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465590
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2726749
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20181011	MGI			PMID:27831556
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001921	reduced fertility		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001924	infertility		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465590
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:2726749
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2726749
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003205	testicular atrophy		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003727	abnormal retina layer morphology		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465590
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465590
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465590
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824473
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824473
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0003993	abnormal ventral spinal root morphology		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824473
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824473
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2726749
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824473
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0005578	teratozoospermia		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787313
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20191010	MGI			PMID:12787314
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824473
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008282	enlarged hippocampus		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1061118
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824473
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:2726749
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:28104815
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465590
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824473
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7891151
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0009280	decreased activated sperm motility		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0009400	decreased skeletal muscle fiber size		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0009434	paraparesis		IEA		N	RGD:5509061	20111116	MGI			
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0009954	abnormal mitral cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884758
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0012490	abnormal cochlear VIII nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2077109
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:28104815
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0020850	abnormal microtubule cytoskeleton morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314854	Agtpbp1	ATP/GTP binding protein 1	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20250807	MGI			PMID:29449678
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160421	MGI			
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20181004	MGI			PMID:30197299
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0011471	decreased urine creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1314856	Mettl16	methyltransferase 16, N6-methyladenosine	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1314858	Mbip	MAP3K12 binding inhibitory protein 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1314858	Mbip	MAP3K12 binding inhibitory protein 1	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240919	MGI			
1314858	Mbip	MAP3K12 binding inhibitory protein 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1314858	Mbip	MAP3K12 binding inhibitory protein 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1314858	Mbip	MAP3K12 binding inhibitory protein 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1314858	Mbip	MAP3K12 binding inhibitory protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1314858	Mbip	MAP3K12 binding inhibitory protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1314860	Lamb1	laminin B1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314860	Lamb1	laminin B1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314860	Lamb1	laminin B1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314860	Lamb1	laminin B1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314860	Lamb1	laminin B1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15102706
1314860	Lamb1	laminin B1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314860	Lamb1	laminin B1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15102706
1314860	Lamb1	laminin B1	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314860	Lamb1	laminin B1	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314860	Lamb1	laminin B1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1314860	Lamb1	laminin B1	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314860	Lamb1	laminin B1	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314860	Lamb1	laminin B1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15102706
1314860	Lamb1	laminin B1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1314860	Lamb1	laminin B1	gene	MP:0011187	abnormal parietal endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15102706
1314860	Lamb1	laminin B1	gene	MP:0012057	abnormal mural trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15102706
1314860	Lamb1	laminin B1	gene	MP:0013179	wavy tail		IAGP		N	RGD:5509061	20180118	MGI			PMID:26705335
1314862	Wnt8a	wingless-type MMTV integration site family, member 8A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041177
1314862	Wnt8a	wingless-type MMTV integration site family, member 8A	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23041177
1314866	Rpl3l	ribosomal protein L3-like	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20230302	MGI			PMID:36733907
1314866	Rpl3l	ribosomal protein L3-like	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20230302	MGI			PMID:36733907
1314866	Rpl3l	ribosomal protein L3-like	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20230601	MGI			PMID:37080962
1314866	Rpl3l	ribosomal protein L3-like	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20230601	MGI			PMID:37080962
1314870	Sec61g	SEC61 translocon subunit gamma	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1314870	Sec61g	SEC61 translocon subunit gamma	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1314870	Sec61g	SEC61 translocon subunit gamma	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241017	MGI			
1314870	Sec61g	SEC61 translocon subunit gamma	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1314870	Sec61g	SEC61 translocon subunit gamma	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314872	Rpl12	ribosomal protein L12	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0000532	kidney vascular congestion		IAGP		N	RGD:5509061	20200402	MGI			PMID:29804851
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0001765	abnormal ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:29804851
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20200402	MGI			PMID:29804851
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0002986	decreased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271117
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21829553
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20200402	MGI			PMID:29804851
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271117
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200402	MGI			PMID:29804851
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271117
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20220811	MGI			
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0004283	absent cornea endothelium		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0005099	abnormal ciliary body morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0005497	optic nerve cupping		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20200402	MGI			PMID:29804851
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21829553
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0006219	optic nerve degeneration		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0009744	postaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21829553
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0009859	eye opacity		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21829553
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0010252	anterior subcapsular cataract		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0010564	abnormal fetal ductus arteriosus morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:29804851
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21829553
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12695560
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271117
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200402	MGI			PMID:29804851
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21829553
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240516	MGI			PMID:32878901
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271117
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0012287	increased frequency of paradoxical sleep		IAGP		N	RGD:5509061	20240516	MGI			PMID:32878901
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0012289	abnormal non-rapid eye movement sleep pattern		IAGP		N	RGD:5509061	20240516	MGI			PMID:32878901
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20240516	MGI			PMID:32878901
1314876	Tfap2b	transcription factor AP-2 beta	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:27483349
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0011426	abnormal ureter smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0011480	impaired ureteric peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776146
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314878	Tshz3	teashirt zinc finger family member 3	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20220428	MGI			PMID:31060802
1314885	Tada3	transcriptional adaptor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22736770
1314885	Tada3	transcriptional adaptor 3	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22736770
1314885	Tada3	transcriptional adaptor 3	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22736770
1314885	Tada3	transcriptional adaptor 3	gene	MP:0010039	abnormal trophoblast giant cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22736770
1314885	Tada3	transcriptional adaptor 3	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22736770
1314885	Tada3	transcriptional adaptor 3	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22736770
1314885	Tada3	transcriptional adaptor 3	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22736770
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170338
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170338
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170338
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170338
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170338
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170338
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170338
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693408
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170338
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332334
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:17693408
1314891	Ing1	inhibitor of growth family, member 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17332334
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0021206	abnormal limb muscle morphology		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314893	Asnsd1	asparagine synthetase domain containing 1	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20240418	MGI			PMID:32638637
1314895	Trmt10c	tRNA methyltransferase 10C, mitochondrial RNase P subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530748
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530748
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530748
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530748
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530748
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530748
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530748
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530748
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0008170	decreased B-1b cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21199920
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530748
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0011816	decreased pre-pro B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314898	Arid3b	AT-rich interaction domain 3B	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27537840
1314900	Acp6	acid phosphatase 6, lysophosphatidic	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1314900	Acp6	acid phosphatase 6, lysophosphatidic	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0003794	delayed somite formation		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0004785	abnormal posterior cardinal vein morphology		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0010951	abnormal lipid oxidation		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0012177	delayed head development		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0012552	lactic acidosis		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0012708	delayed rostral neuropore closure		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0013906	absent embryonic telencephalon		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0014012	abnormal cranial blood vasculature morphology		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20230406	MGI			PMID:36693621
1314902	Hacd2	3-hydroxyacyl-CoA dehydratase 2	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:36693621
1314905	Zfp110	zinc finger protein 110	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545116
1314905	Zfp110	zinc finger protein 110	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545116
1314905	Zfp110	zinc finger protein 110	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545116
1314905	Zfp110	zinc finger protein 110	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545116
1314905	Zfp110	zinc finger protein 110	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545116
1314905	Zfp110	zinc finger protein 110	gene	MP:0030006	decreased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:10545116
1314906	Diaph3	diaphanous related formin 3	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20201002	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239357
1314906	Diaph3	diaphanous related formin 3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20201002	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20160811	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20160811	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20201002	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20201002	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239357
1314906	Diaph3	diaphanous related formin 3	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20160811	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0002546	mydriasis		IEA		N	RGD:5509061	20210520	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20160421	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20201002	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20220519	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20220519	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20201002	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20201002	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239357
1314906	Diaph3	diaphanous related formin 3	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20201002	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160421	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20201002	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239357
1314906	Diaph3	diaphanous related formin 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20201001	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314906	Diaph3	diaphanous related formin 3	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239357
1314906	Diaph3	diaphanous related formin 3	gene	MP:0012397	abnormal nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239357
1314906	Diaph3	diaphanous related formin 3	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:26471482
1314906	Diaph3	diaphanous related formin 3	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:26471482
1314910	Tvp23b	trans-golgi network vesicle protein 23B	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1314910	Tvp23b	trans-golgi network vesicle protein 23B	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20231102	MGI			PMID:37339972
1314910	Tvp23b	trans-golgi network vesicle protein 23B	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20231102	MGI			PMID:37339972
1314910	Tvp23b	trans-golgi network vesicle protein 23B	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20231102	MGI			PMID:37339972
1314910	Tvp23b	trans-golgi network vesicle protein 23B	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20231102	MGI			PMID:37339972
1314910	Tvp23b	trans-golgi network vesicle protein 23B	gene	MP:0013799	abnormal intestinal goblet cell physiology		IAGP		N	RGD:5509061	20231102	MGI			PMID:37339972
1314910	Tvp23b	trans-golgi network vesicle protein 23B	gene	MP:0014222	decreased colon goblet cell number		IAGP		N	RGD:5509061	20231102	MGI			PMID:37339972
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20250515	MGI			PMID:38016036
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20250515	MGI			PMID:38016036
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20250515	MGI			PMID:38016036
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20250515	MGI			PMID:31685995
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20250515	MGI			PMID:38016036
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20250515	MGI			PMID:31685995
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20250515	MGI			PMID:31685995
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20250515	MGI			PMID:38016036
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0008618	decreased circulating interleukin-12 level		IAGP		N	RGD:5509061	20250515	MGI			PMID:38016036
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20250515	MGI			PMID:31685995
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20250515	MGI			PMID:31685995
1314911	Znfx1	zinc finger, NFX1-type containing 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20250515	MGI			PMID:38016036
1314914	Ubxn7	UBX domain protein 7	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20190502	MGI			
1314914	Ubxn7	UBX domain protein 7	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1314914	Ubxn7	UBX domain protein 7	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1314914	Ubxn7	UBX domain protein 7	gene	MP:0009931	abnormal skin appearance		IEA		N	RGD:5509061	20190502	MGI			
1314914	Ubxn7	UBX domain protein 7	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1314914	Ubxn7	UBX domain protein 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314914	Ubxn7	UBX domain protein 7	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20170105	MGI			
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002673	abnormal sperm number		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20181227	MGI			
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0006236	absent Meibomian glands		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20170105	MGI			
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008258	thin endometrium		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0009669	abnormal postimplantation uterine environment		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0010855	pulmonary hyperemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24012418
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0013192	decreased sebaceous gland number		IAGP		N	RGD:5509061	20160317	MGI			PMID:26333994
1314919	Ash1l	ASH1 like histone lysine methyltransferase	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20211021	MGI			
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20211021	MGI			
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0010906	abnormal lung bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956870
1314920	Tmtc3	transmembrane and tetratricopeptide repeat containing 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314922	Fbxo3	F-box protein 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1314925	Svil	supervillin	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550155
1314925	Svil	supervillin	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550155
1314925	Svil	supervillin	gene	MP:0009586	increased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550155
1314925	Svil	supervillin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20160804	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20160804	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0005316	abnormal response to tactile stimuli		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20141003	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20160804	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20160804	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0008805	decreased circulating amylase level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314927	Slc38a10	solute carrier family 38, member 10	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190926	MGI			PMID:28945193
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20190926	MGI			PMID:28945193
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210826	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20211021	MGI			
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0004182	abnormal spermiation		IAGP		N	RGD:5509061	20190926	MGI			PMID:28945193
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20190926	MGI			PMID:28945193
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:28945193
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20190926	MGI			PMID:28945193
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:28945193
1314929	Sun5	Sad1 and UNC84 domain containing 5	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:28945193
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793587
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793587
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793587
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793587
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793587
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0011045	decreased lung elastance		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20241121	MGI			
1314933	Chfr	checkpoint with forkhead and ring finger domains	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793587
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141030	MGI			PMID:24385930
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20200514	MGI			
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921919
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141030	MGI			PMID:24385930
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160204	MGI			PMID:25866966
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11895368
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141030	MGI			PMID:24385930
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160204	MGI			PMID:25866966
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20160204	MGI			PMID:25866966
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11895368
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20160204	MGI			PMID:25866966
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921919
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921919
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22916201
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20201022	MGI			
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921919
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921919
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11895368
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141030	MGI			PMID:24385930
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20160204	MGI			PMID:25866966
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590147
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141030	MGI			PMID:24385930
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20160204	MGI			PMID:25866966
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20230907	MGI			PMID:37389991
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20200514	MGI			
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20170413	MGI			PMID:26869263
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20230907	MGI			PMID:37389991
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17940072
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20160204	MGI			PMID:25866966
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0003356	impaired luteinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20160204	MGI			PMID:25866966
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0003666	impaired sperm capacitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0003962	abnormal adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22916201
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20170413	MGI			PMID:26869263
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0004962	decreased prostate gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921919
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11756548
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17940072
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:11895368
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590147
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:15921919
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11895368
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141030	MGI			PMID:24385930
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22916201
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20210128	MGI			
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808466
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20200514	MGI			
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:15921919
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0020870	decreased thigmotaxis		IAGP		N	RGD:5509061	20230907	MGI			PMID:37389991
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20230907	MGI			PMID:37389991
1314935	Ube3a	ubiquitin protein ligase E3A	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20230907	MGI			PMID:37389991
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20231207	MGI			
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20231207	MGI			
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0002649	abnormal enamel rod pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20160114	MGI			
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0006133	calcified artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0010923	calcified pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0011309	abnormal kidney arterial blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0030138	abnormal lower incisor color		IAGP		N	RGD:5509061	20171005	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0030139	abnormal upper incisor color		IAGP		N	RGD:5509061	20171005	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0030458	abnormal tooth wear		IAGP		N	RGD:5509061	20171228	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0030460	enamel pits		IAGP		N	RGD:5509061	20171221	MGI			PMID:22732358
1314940	Fam20a	FAM20A, golgi associated secretory pathway pseudokinase	gene	MP:0030500	conical molar		IAGP		N	RGD:5509061	20171228	MGI			PMID:22732358
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20141003	MGI			
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20210826	MGI			
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0008103	amacrine cell degeneration		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0008265	abnormal hippocampus CA2 region morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:25061210
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1314944	Gtpbp2	GTP binding protein 2	gene	MP:0021081	abnormal ribosomal stalling		IAGP		N	RGD:5509061	20220310	MGI			PMID:25061210
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692052
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692051
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692051
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210826	MGI			
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692052
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14560001
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692051
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898471
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0002467	impaired neutrophil phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407890
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19218085
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008132	increased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008136	enlarged Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898471
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692052
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008599	increased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692052
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692052
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:14560001
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692051
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565376
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15692052
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1314946	Nod2	nucleotide-binding oligomerization domain containing 2	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20240627	MGI			
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20181108	MGI			PMID:26755066
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20220428	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0004043	abnormal pH regulation		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0011000	abnormal allogrooming behavior		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0011617	abnormal habituation		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20181108	MGI			PMID:26755066
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20181108	MGI			PMID:26755066
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0020396	abnormal social recognition		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0020437	abnormal social play behavior		IAGP		N	RGD:5509061	20181025	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0020852	abnormal olfactory behavior		IAGP		N	RGD:5509061	20181101	MGI			PMID:29362376
1314948	Slc9a9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	gene	MP:0030950	abnormal synaptic vesicle exocytosis		IAGP		N	RGD:5509061	20190725	MGI			PMID:29362376
1314954	Mgst3	microsomal glutathione S-transferase 3	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1314954	Mgst3	microsomal glutathione S-transferase 3	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20150827	MGI			PMID:24859200
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20150827	MGI			PMID:24859200
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24859200
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20150827	MGI			PMID:24859200
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20181227	MGI			
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20181227	MGI			
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24859200
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24859200
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20150827	MGI			PMID:24859200
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0011724	ectopic cortical neuron		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0012474	decreased cingulate cortex size		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0012506	brain atrophy		IAGP		N	RGD:5509061	20150618	MGI			PMID:18562329
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0013908	small lateral ventricles		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0020762	abnormal dorsal subiculum morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31173351
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32221352
1314955	Eml1	echinoderm microtubule associated protein like 1	gene	MP:0030245	round head		IEA		N	RGD:5509061	20190418	MGI			
1314959	Alkbh2	alkB homolog 2, alpha-ketoglutarate-dependent dioxygenase	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16642038
1314959	Alkbh2	alkB homolog 2, alpha-ketoglutarate-dependent dioxygenase	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:16642038
1314961	Kdm4a	lysine (K)-specific demethylase 4A	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555854
1314961	Kdm4a	lysine (K)-specific demethylase 4A	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555854
1314961	Kdm4a	lysine (K)-specific demethylase 4A	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555854
1314961	Kdm4a	lysine (K)-specific demethylase 4A	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555854
1314961	Kdm4a	lysine (K)-specific demethylase 4A	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555854
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0014454	increased hormone level		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314964	Gulp1	GULP, engulfment adaptor PTB domain containing 1	gene	MP:0031073	decreased circulating type I collagen C-terminal telopeptide level		IAGP		N	RGD:5509061	20250313	MGI			PMID:36870066
1314967	Taf1b	TATA-box binding protein associated factor, RNA polymerase I, B	gene	MP:0008830	abnormal nucleolus morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:35139074
1314967	Taf1b	TATA-box binding protein associated factor, RNA polymerase I, B	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220324	MGI			PMID:35139074
1314967	Taf1b	TATA-box binding protein associated factor, RNA polymerase I, B	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20220324	MGI			PMID:35139074
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201231	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009202
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20180215	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148099
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009202
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148099
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148099
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244019
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002491	decreased IgD level		IEA		N	RGD:5509061	20181004	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20180215	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002494	increased IgM level		IEA		N	RGD:5509061	20181004	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148099
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20181227	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20251113	MGI			PMID:40796308
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210128	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20180215	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244019
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244019
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0005425	increased macrophage cell number		IEA		N	RGD:5509061	20180215	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148099
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0006173	abnormal myeloid dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181004	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008125	abnormal dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008170	decreased B-1b cell number		IEA		N	RGD:5509061	20180215	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244019
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244019
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008196	abnormal follicular dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008240	abnormal spleen marginal zone macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9009202
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133427
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244019
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244019
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20181004	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0010848	decreased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1314972	Bcl3	B cell leukemia/lymphoma 3	gene	MP:0014350	disorganized spleen B cell follicle		IAGP		N	RGD:5509061	20240104	MGI			PMID:9133427
1314974	Mrpl18	mitochondrial ribosomal protein L18	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1314974	Mrpl18	mitochondrial ribosomal protein L18	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1314974	Mrpl18	mitochondrial ribosomal protein L18	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314974	Mrpl18	mitochondrial ribosomal protein L18	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1314976	Klhl2	kelch-like 2, Mayven	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20191010	MGI			PMID:28414128
1314976	Klhl2	kelch-like 2, Mayven	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20241121	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363391
1314978	Foxn4	forkhead box N4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363391
1314978	Foxn4	forkhead box N4	gene	MP:0006070	increased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363391
1314978	Foxn4	forkhead box N4	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363391
1314978	Foxn4	forkhead box N4	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363391
1314978	Foxn4	forkhead box N4	gene	MP:0008107	absent retina horizontal cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363391
1314978	Foxn4	forkhead box N4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20241121	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20241121	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20241121	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363391
1314978	Foxn4	forkhead box N4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20241121	MGI			
1314978	Foxn4	forkhead box N4	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:15363391
1314980	Cab39	calcium binding protein 39	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20250508	MGI			
1314980	Cab39	calcium binding protein 39	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20200924	MGI			PMID:32341096
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200924	MGI			PMID:32341096
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20230601	MGI			
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0008912	nervous		IAGP		N	RGD:5509061	20200723	MGI			PMID:21217823
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200924	MGI			PMID:32341096
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0012315	impaired learning		IAGP		N	RGD:5509061	20200924	MGI			PMID:32341096
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1314982	Mrpl3	mitochondrial ribosomal protein L3	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260716	MGI			PMID:32376682
1314988	Tctn2	tectonic family member 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565611
1314988	Tctn2	tectonic family member 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565611
1314988	Tctn2	tectonic family member 2	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565611
1314988	Tctn2	tectonic family member 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565611
1314988	Tctn2	tectonic family member 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565611
1314988	Tctn2	tectonic family member 2	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1314988	Tctn2	tectonic family member 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1314988	Tctn2	tectonic family member 2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1314988	Tctn2	tectonic family member 2	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565611
1314988	Tctn2	tectonic family member 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565611
1314988	Tctn2	tectonic family member 2	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565611
1314988	Tctn2	tectonic family member 2	gene	MP:0011261	abnormal limb mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1314989	Cpsf4l	cleavage and polyadenylation specific factor 4-like	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1314993	Ccnj	cyclin J	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1314993	Ccnj	cyclin J	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1314993	Ccnj	cyclin J	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314993	Ccnj	cyclin J	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314993	Ccnj	cyclin J	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314993	Ccnj	cyclin J	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314993	Ccnj	cyclin J	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314993	Ccnj	cyclin J	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314993	Ccnj	cyclin J	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314993	Ccnj	cyclin J	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314993	Ccnj	cyclin J	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314993	Ccnj	cyclin J	gene	MP:0014433	increased cytokine level		IAGP		N	RGD:5509061	20260430	MGI			PMID:35412849
1314996	Cnot8	CCR4-NOT transcription complex, subunit 8	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20210513	MGI			PMID:31924127
1314996	Cnot8	CCR4-NOT transcription complex, subunit 8	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20210513	MGI			PMID:31924127
1314997	Pus10	pseudouridylate synthase 10	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1315003	Isg20	interferon-stimulated protein	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20240620	MGI			PMID:37452495
1315003	Isg20	interferon-stimulated protein	gene	MP:0004041	increased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20240620	MGI			PMID:37452495
1315003	Isg20	interferon-stimulated protein	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20240620	MGI			PMID:37452495
1315003	Isg20	interferon-stimulated protein	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20240620	MGI			PMID:37452495
1315005	Kcmf1	potassium channel modulatory factor 1	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473331
1315005	Kcmf1	potassium channel modulatory factor 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473331
1315005	Kcmf1	potassium channel modulatory factor 1	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473331
1315005	Kcmf1	potassium channel modulatory factor 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473331
1315005	Kcmf1	potassium channel modulatory factor 1	gene	MP:0009109	decreased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473331
1315005	Kcmf1	potassium channel modulatory factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473331
1315005	Kcmf1	potassium channel modulatory factor 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473331
1315009	Serf2	small EDRK-rich factor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315011	Pop7	processing of precursor 7, ribonuclease P family, (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1315011	Pop7	processing of precursor 7, ribonuclease P family, (S. cerevisiae)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20190808	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190808	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23632887
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20190808	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20250508	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20190808	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0013669	decreased Ly6C-positive immature NK cell number		IEA		N	RGD:5509061	20201022	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0013670	increased Ly6C-positive immature NK cell number		IEA		N	RGD:5509061	20201022	MGI			
1315013	Asb2	ankyrin repeat and SOCS box-containing 2	gene	MP:0031723	abnormal podosome assembly		IAGP		N	RGD:5509061	20260507	MGI			PMID:23632887
1315017	Epn3	epsin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115825
1315017	Epn3	epsin 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1315017	Epn3	epsin 3	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0020070	decreased neocortex volume		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315023	Elp2	elongator acetyltransferase complex subunit 2	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20210909	MGI			PMID:33976153
1315025	Klk7	kallikrein related-peptidase 7 (chymotryptic, stratum corneum)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180628	MGI			PMID:29311134
1315025	Klk7	kallikrein related-peptidase 7 (chymotryptic, stratum corneum)	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180628	MGI			PMID:29311134
1315028	Cct7	chaperonin containing TCP1 subunit 7	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20240523	MGI			
1315028	Cct7	chaperonin containing TCP1 subunit 7	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20240926	MGI			
1315028	Cct7	chaperonin containing TCP1 subunit 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1315028	Cct7	chaperonin containing TCP1 subunit 7	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1315028	Cct7	chaperonin containing TCP1 subunit 7	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1315031	Snx17	sorting nexin 17	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20141003	MGI			
1315031	Snx17	sorting nexin 17	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1315031	Snx17	sorting nexin 17	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20141003	MGI			
1315031	Snx17	sorting nexin 17	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1315031	Snx17	sorting nexin 17	gene	MP:0011661	persistent truncus arteriosus type i		IEA		N	RGD:5509061	20141003	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20160825	MGI			PMID:27225478
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20210520	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20241121	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210520	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20210826	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20250508	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220519	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20160825	MGI			PMID:27225478
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20160825	MGI			PMID:27225478
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20160825	MGI			PMID:27225478
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0010580	decreased heart left ventricle size		IAGP		N	RGD:5509061	20160825	MGI			PMID:27225478
1315033	Dusp8	dual specificity phosphatase 8	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20160825	MGI			PMID:27225478
1315035	Ca9	carbonic anhydrase 9	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16217040
1315035	Ca9	carbonic anhydrase 9	gene	MP:0002580	duodenal lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454846
1315035	Ca9	carbonic anhydrase 9	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16217040
1315035	Ca9	carbonic anhydrase 9	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454846
1315035	Ca9	carbonic anhydrase 9	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16217040
1315035	Ca9	carbonic anhydrase 9	gene	MP:0005493	stomach epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454846
1315035	Ca9	carbonic anhydrase 9	gene	MP:0005493	stomach epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16217040
1315035	Ca9	carbonic anhydrase 9	gene	MP:0008210	increased mature B cell number		IEA		N	RGD:5509061	20170323	MGI			
1315035	Ca9	carbonic anhydrase 9	gene	MP:0010787	gastric cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16217040
1315035	Ca9	carbonic anhydrase 9	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454846
1315035	Ca9	carbonic anhydrase 9	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16217040
1315035	Ca9	carbonic anhydrase 9	gene	MP:0013567	gastric gland atrophy		IAGP		N	RGD:5509061	20150312	MGI			PMID:16217040
1315041	Nmb	neuromedin B	gene	MP:0001440	abnormal grooming behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:29133874
1315041	Nmb	neuromedin B	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1315044	Map3k5	mitogen-activated protein kinase kinase kinase 5	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665690
1315044	Map3k5	mitogen-activated protein kinase kinase kinase 5	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665690
1315044	Map3k5	mitogen-activated protein kinase kinase kinase 5	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19214184
1315044	Map3k5	mitogen-activated protein kinase kinase kinase 5	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266364
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000215	absent erythrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210520	MGI			
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20595512
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17826737
1315048	Rapgef2	Rap guanine nucleotide exchange factor (GEF) 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1315051	Rabl3	RAB, member RAS oncogene family-like 3	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200730	MGI			PMID:32220963
1315051	Rabl3	RAB, member RAS oncogene family-like 3	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20200730	MGI			PMID:32220963
1315051	Rabl3	RAB, member RAS oncogene family-like 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20200730	MGI			PMID:32220963
1315051	Rabl3	RAB, member RAS oncogene family-like 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200730	MGI			PMID:32220963
1315051	Rabl3	RAB, member RAS oncogene family-like 3	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20200730	MGI			PMID:32220963
1315051	Rabl3	RAB, member RAS oncogene family-like 3	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20200730	MGI			PMID:32220963
1315051	Rabl3	RAB, member RAS oncogene family-like 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20200730	MGI			PMID:32220963
1315051	Rabl3	RAB, member RAS oncogene family-like 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200730	MGI			PMID:32220963
1315051	Rabl3	RAB, member RAS oncogene family-like 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200730	MGI			PMID:32220963
1315053	Spryd7	SPRY domain containing 7	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20250508	MGI			
1315053	Spryd7	SPRY domain containing 7	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1315055	Tent2	terminal nucleotidyltransferase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1315055	Tent2	terminal nucleotidyltransferase 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20250508	MGI			
1315055	Tent2	terminal nucleotidyltransferase 2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20250508	MGI			
1315055	Tent2	terminal nucleotidyltransferase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1315055	Tent2	terminal nucleotidyltransferase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20250508	MGI			
1315055	Tent2	terminal nucleotidyltransferase 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20250508	MGI			
1315055	Tent2	terminal nucleotidyltransferase 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20250508	MGI			
1315055	Tent2	terminal nucleotidyltransferase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927953
1315055	Tent2	terminal nucleotidyltransferase 2	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20250508	MGI			
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20241121	MGI			
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20210121	MGI			PMID:33086058
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20210121	MGI			PMID:33086058
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20210121	MGI			PMID:33086058
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20210121	MGI			PMID:33086058
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210121	MGI			PMID:33086058
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0011371	decreased kidney apoptosis		IAGP		N	RGD:5509061	20210121	MGI			PMID:33086058
1315059	Sh3yl1	Sh3 domain YSC-like 1	gene	MP:0011372	decreased renal tubule apoptosis		IAGP		N	RGD:5509061	20210121	MGI			PMID:33086058
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20260402	MGI			
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20260402	MGI			
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002905	decreased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0003195	calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0003196	calcified skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0010522	calcified aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0010964	increased compact bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213845
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0011585	decreased alkaline phosphatase activity		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0012337	increased vitamin D level		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20170713	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0031197	calcified testicular artery		IAGP		N	RGD:5509061	20201119	MGI			PMID:22912827
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315064	Galnt3	polypeptide N-acetylgalactosaminyltransferase 3	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20220407	MGI			PMID:23052838
1315068	Tmprss11g	transmembrane protease, serine 11g	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20191031	MGI			PMID:31501243
1315070	Samd8	sterile alpha motif domain containing 8	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20170824	MGI			PMID:25605874
1315070	Samd8	sterile alpha motif domain containing 8	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20170824	MGI			PMID:25605874
1315070	Samd8	sterile alpha motif domain containing 8	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20170824	MGI			PMID:25667419
1315070	Samd8	sterile alpha motif domain containing 8	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20170824	MGI			PMID:25605874
1315070	Samd8	sterile alpha motif domain containing 8	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20170824	MGI			PMID:25667419
1315070	Samd8	sterile alpha motif domain containing 8	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:25667419
1315073	Stk33	serine/threonine kinase 33	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20191114	MGI			PMID:29155043
1315073	Stk33	serine/threonine kinase 33	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20191114	MGI			PMID:29155043
1315073	Stk33	serine/threonine kinase 33	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1315073	Stk33	serine/threonine kinase 33	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:29155043
1315073	Stk33	serine/threonine kinase 33	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1315075	Psmd11	proteasome (prosome, macropain) 26S subunit, non-ATPase, 11	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240613	MGI			PMID:33517884
1315075	Psmd11	proteasome (prosome, macropain) 26S subunit, non-ATPase, 11	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20240613	MGI			PMID:33517884
1315075	Psmd11	proteasome (prosome, macropain) 26S subunit, non-ATPase, 11	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20240613	MGI			PMID:33517884
1315075	Psmd11	proteasome (prosome, macropain) 26S subunit, non-ATPase, 11	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240613	MGI			PMID:33517884
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20250508	MGI			
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20160811	MGI			
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039116
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039116
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478856
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754961
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807948
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754961
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807948
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754961
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807948
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22549958
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754961
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754961
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24532689
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20250508	MGI			
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0003572	abnormal uterus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20170601	MGI			PMID:26742488
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039116
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20170601	MGI			PMID:26742488
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478856
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807948
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039116
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141030	MGI			PMID:22530760
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694567
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478856
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807948
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761591
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23318132
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141030	MGI			PMID:22530760
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478856
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22549958
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039116
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11106738
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694567
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23318132
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20170601	MGI			PMID:26742488
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20231123	MGI			PMID:37891173
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141030	MGI			PMID:22530760
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478856
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807948
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754961
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20170615	MGI			PMID:27760146
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754961
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20170615	MGI			PMID:27760146
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20210304	MGI			PMID:30853435
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754961
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870400
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11106739
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:24589552
1315082	Spo11	SPO11 initiator of meiotic double stranded breaks	gene	MP:0031474	increased female germ cell apoptosis		IAGP		N	RGD:5509061	20230615	MGI			PMID:21478856
1315085	Art4	ADP-ribosyltransferase 4	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1315088	Clstn1	calsyntenin 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20160421	MGI			
1315088	Clstn1	calsyntenin 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20151022	MGI			PMID:24966372
1315088	Clstn1	calsyntenin 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1315088	Clstn1	calsyntenin 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1315088	Clstn1	calsyntenin 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1315088	Clstn1	calsyntenin 1	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20151022	MGI			PMID:24966372
1315088	Clstn1	calsyntenin 1	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20151022	MGI			PMID:24966372
1315088	Clstn1	calsyntenin 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20151022	MGI			PMID:24966372
1315088	Clstn1	calsyntenin 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20151022	MGI			PMID:24966372
1315088	Clstn1	calsyntenin 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20151022	MGI			PMID:24966372
1315088	Clstn1	calsyntenin 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20151022	MGI			PMID:24966372
1315088	Clstn1	calsyntenin 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1315088	Clstn1	calsyntenin 1	gene	MP:0011273	prolonged excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20151022	MGI			PMID:24966372
1315088	Clstn1	calsyntenin 1	gene	MP:0014379	decreased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:24966372
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200521	MGI			PMID:32194851
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200521	MGI			PMID:32194851
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141009	MGI			PMID:24870235
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141009	MGI			PMID:24870235
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141009	MGI			PMID:24870235
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141009	MGI			PMID:24870235
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141009	MGI			PMID:24870235
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20141009	MGI			PMID:24870235
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20200521	MGI			PMID:32194851
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141009	MGI			PMID:24870235
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24870235
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0013219	abnormal substantia nigra pars compacta morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:32194851
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:24870235
1315090	Cntnap4	contactin associated protein-like 4	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20200521	MGI			PMID:32194851
1315092	Gpr63	G protein-coupled receptor 63	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1315092	Gpr63	G protein-coupled receptor 63	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200416	MGI			PMID:31730647
1315092	Gpr63	G protein-coupled receptor 63	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1315092	Gpr63	G protein-coupled receptor 63	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1315092	Gpr63	G protein-coupled receptor 63	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1315092	Gpr63	G protein-coupled receptor 63	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1315092	Gpr63	G protein-coupled receptor 63	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1315092	Gpr63	G protein-coupled receptor 63	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1315092	Gpr63	G protein-coupled receptor 63	gene	MP:0012547	spina bifida cystica		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21925315
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:21925315
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20200402	MGI			
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20200402	MGI			
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21925315
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0003671	abnormal eyelid aperture		IEA		N	RGD:5509061	20201231	MGI			
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21925315
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200402	MGI			
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21925315
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21925315
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0014619	absent spermatogonia		IAGP		N	RGD:5509061	20250220	MGI			PMID:19217432
1315094	Usp1	ubiquitin specific peptidase 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19217432
1315095	Ttll8	tubulin tyrosine ligase-like family, member 8	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210422	MGI			PMID:33414192
1315095	Ttll8	tubulin tyrosine ligase-like family, member 8	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210422	MGI			PMID:33414192
1315095	Ttll8	tubulin tyrosine ligase-like family, member 8	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20210422	MGI			PMID:33414192
1315095	Ttll8	tubulin tyrosine ligase-like family, member 8	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20210422	MGI			PMID:33414192
1315095	Ttll8	tubulin tyrosine ligase-like family, member 8	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210422	MGI			PMID:33414192
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0000928	incomplete rostral neuropore closure		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0004180	failure of initiation of embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20221215	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0009657	failure of chorioallantoic fusion		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1315098	Slc30a9	solute carrier family 30 (zinc transporter), member 9	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220811	MGI			
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:13892780
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:5798244
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518730
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518730
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20150101	MGI			PMID:17008558
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9680329
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12395314
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10225971
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9680329
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10225971
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518730
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9680329
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0002534	abnormal type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518730
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0002534	abnormal type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9680329
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20150101	MGI			PMID:17008558
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20150101	MGI			PMID:17008558
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518730
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20150101	MGI			PMID:17008558
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20150101	MGI			PMID:17008558
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518730
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20150101	MGI			PMID:17008558
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10225971
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:13892780
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17008558
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:5798244
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0020935	decreased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:13892780
1315100	Mst1r	macrophage stimulating 1 receptor (c-met-related tyrosine kinase)	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:14505749
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669418
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297047
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294162
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250413
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297047
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0001819	abnormal immune cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18412166
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669418
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669418
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669417
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669418
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041586
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18412166
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669418
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294162
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297047
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250413
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0004867	decreased platelet calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705797
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250413
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483449
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294162
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483449
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705797
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297047
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250413
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669418
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294162
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041586
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18412166
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669416
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669417
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669418
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041586
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720808
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18412166
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20170713	MGI			PMID:25605974
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705797
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19515725
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250413
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0020928	increased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18250413
1315104	Pik3cg	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:15705797
1315108	Il19	interleukin 19	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315108	Il19	interleukin 19	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160512	MGI			PMID:25794104
1315111	Mtx2	metaxin 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210826	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20240919	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20240919	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20240919	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20240919	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20240919	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1315111	Mtx2	metaxin 2	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1315112	Lyz3	lysozyme 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230720	MGI			
1315112	Lyz3	lysozyme 3	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20231207	MGI			
1315112	Lyz3	lysozyme 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230720	MGI			
1315112	Lyz3	lysozyme 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230720	MGI			
1315112	Lyz3	lysozyme 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1315115	Rhbdd1	rhomboid domain containing 1	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20240404	MGI			PMID:38453906
1315115	Rhbdd1	rhomboid domain containing 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20240404	MGI			PMID:38453906
1315115	Rhbdd1	rhomboid domain containing 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20240404	MGI			PMID:38453906
1315115	Rhbdd1	rhomboid domain containing 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20240404	MGI			PMID:38453906
1315115	Rhbdd1	rhomboid domain containing 1	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:35436469
1315115	Rhbdd1	rhomboid domain containing 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20240404	MGI			PMID:38453906
1315115	Rhbdd1	rhomboid domain containing 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20240404	MGI			PMID:35436469
1315115	Rhbdd1	rhomboid domain containing 1	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20240404	MGI			PMID:35436469
1315115	Rhbdd1	rhomboid domain containing 1	gene	MP:0031265	increased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:35436469
1315117	Rab20	RAB20, member RAS oncogene family	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28494243
1315117	Rab20	RAB20, member RAS oncogene family	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20220811	MGI			
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0001785	edema		IEA		N	RGD:5509061	20220519	MGI			
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20220519	MGI			
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0003846	matted coat		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20220519	MGI			
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38011999
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:38011999
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20241121	MGI			
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315119	Eif4b	eukaryotic translation initiation factor 4B	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1315123	Txk	TXK tyrosine kinase	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213685
1315123	Txk	TXK tyrosine kinase	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1315123	Txk	TXK tyrosine kinase	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213685
1315123	Txk	TXK tyrosine kinase	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213685
1315123	Txk	TXK tyrosine kinase	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1315123	Txk	TXK tyrosine kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213685
1315123	Txk	TXK tyrosine kinase	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1315123	Txk	TXK tyrosine kinase	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213685
1315123	Txk	TXK tyrosine kinase	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0002679	abnormal corpus luteum morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0004018	abnormal galactose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11286504
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0004018	abnormal galactose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8902187
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0004018	abnormal galactose homeostasis		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0011854	cerebral edema		IAGP		N	RGD:5509061	20180809	MGI			PMID:24549051
1315127	Galt	galactose-1-phosphate uridyl transferase	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:24549051
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20171005	MGI			PMID:26428007
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20171005	MGI			PMID:26428007
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0011124	increased primary ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20171005	MGI			PMID:26428007
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0031383	increased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:34972250
1315130	Bcas2	BCAS2 pre-mRNA processing factor	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:34972250
1315132	Habp4	hyaluronic acid binding protein 4	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20211014	MGI			PMID:33245729
1315132	Habp4	hyaluronic acid binding protein 4	gene	MP:0014201	abnormal intestinal epithelium physiology		IAGP		N	RGD:5509061	20211014	MGI			PMID:33245729
1315133	Rab3gap1	RAB3 GTPase activating protein subunit 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1315133	Rab3gap1	RAB3 GTPase activating protein subunit 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1315133	Rab3gap1	RAB3 GTPase activating protein subunit 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782817
1315133	Rab3gap1	RAB3 GTPase activating protein subunit 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782817
1315133	Rab3gap1	RAB3 GTPase activating protein subunit 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1315133	Rab3gap1	RAB3 GTPase activating protein subunit 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1315133	Rab3gap1	RAB3 GTPase activating protein subunit 1	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782817
1315133	Rab3gap1	RAB3 GTPase activating protein subunit 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1315135	Appbp2	amyloid beta precursor protein binding protein 2	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20201022	MGI			
1315135	Appbp2	amyloid beta precursor protein binding protein 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201022	MGI			
1315135	Appbp2	amyloid beta precursor protein binding protein 2	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1315135	Appbp2	amyloid beta precursor protein binding protein 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1315135	Appbp2	amyloid beta precursor protein binding protein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1315137	Rab5b	RAB5B, member RAS oncogene family	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1315137	Rab5b	RAB5B, member RAS oncogene family	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1315137	Rab5b	RAB5B, member RAS oncogene family	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20260402	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20260402	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20260402	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0001785	edema		IEA		N	RGD:5509061	20260402	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20260402	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20260402	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20260402	MGI			
1315139	Zfp710	zinc finger protein 710	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20260402	MGI			
1315141	Nin	ninein	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0001238	thin epidermis stratum spinosum		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210128	MGI			
1315141	Nin	ninein	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1315141	Nin	ninein	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20170105	MGI			
1315141	Nin	ninein	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1315141	Nin	ninein	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20170105	MGI			
1315141	Nin	ninein	gene	MP:0009441	delayed skin barrier formation		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0009598	thin epidermis stratum granulosum		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0009605	decreased keratohyalin granule number		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0009607	decreased keratohyalin granule size		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0009608	abnormal epidermal lamellar body morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0009714	thin epidermis stratum basale		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315141	Nin	ninein	gene	MP:0030605	abnormal corneocyte morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30923192
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20220519	MGI			
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20220519	MGI			
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220519	MGI			
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20220519	MGI			
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0012270	cardiac edema		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220519	MGI			
1315142	Dync2i1	dynein 2 intermediate chain 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1315143	Vopp1	vesicular, overexpressed in cancer, prosurvival protein 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20201231	MGI			
1315143	Vopp1	vesicular, overexpressed in cancer, prosurvival protein 1	gene	MP:0002546	mydriasis		IEA		N	RGD:5509061	20240523	MGI			
1315143	Vopp1	vesicular, overexpressed in cancer, prosurvival protein 1	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20231207	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220519	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1315146	Rad1	RAD1 checkpoint DNA exonuclease	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1315152	Knop1	lysine rich nucleolar protein 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20190502	MGI			
1315152	Knop1	lysine rich nucleolar protein 1	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1315152	Knop1	lysine rich nucleolar protein 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20220811	MGI			
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0005380	embryo phenotype		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0005387	immune system phenotype		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0008651	increased interleukin-1 secretion		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315156	Socs4	suppressor of cytokine signaling 4	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240229	MGI			PMID:24809749
1315158	Klhdc2	kelch domain containing 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20160421	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20160421	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20141003	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20141003	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20141003	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20141003	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20170105	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1315158	Klhdc2	kelch domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315162	Rad54b	RAD54 homolog B (S. cerevisiae)	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428451
1315162	Rad54b	RAD54 homolog B (S. cerevisiae)	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428451
1315162	Rad54b	RAD54 homolog B (S. cerevisiae)	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428451
1315162	Rad54b	RAD54 homolog B (S. cerevisiae)	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428451
1315164	Erlec1	endoplasmic reticulum lectin 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1315164	Erlec1	endoplasmic reticulum lectin 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1315164	Erlec1	endoplasmic reticulum lectin 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1315164	Erlec1	endoplasmic reticulum lectin 1	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20191128	MGI			
1315164	Erlec1	endoplasmic reticulum lectin 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20221215	MGI			
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241017	MGI			
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0002718	abnormal inner cell mass morphology		IEA		N	RGD:5509061	20241017	MGI			
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1315166	Ruvbl2	RuvB-like AAA ATPase 2	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1315170	Hoxd10	homeobox D10	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409668
1315170	Hoxd10	homeobox D10	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409668
1315170	Hoxd10	homeobox D10	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409668
1315170	Hoxd10	homeobox D10	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1315170	Hoxd10	homeobox D10	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409668
1315170	Hoxd10	homeobox D10	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1315170	Hoxd10	homeobox D10	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1315170	Hoxd10	homeobox D10	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409668
1315170	Hoxd10	homeobox D10	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409668
1315170	Hoxd10	homeobox D10	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0003856	abnormal hindlimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0004600	abnormal vertebral transverse process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409668
1315170	Hoxd10	homeobox D10	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409668
1315170	Hoxd10	homeobox D10	gene	MP:0004654	absent lumbar vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0004694	absent patella		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1315170	Hoxd10	homeobox D10	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9409668
1315170	Hoxd10	homeobox D10	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0009005	abnormal sesamoid bone of gastrocnemius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315170	Hoxd10	homeobox D10	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10642795
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0011016	increased core body temperature		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0011019	abnormal adaptive thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20180111	MGI			PMID:24072708
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0014476	abnormal feces lipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20160421	MGI			PMID:22345407
1315173	Acot13	acyl-CoA thioesterase 13	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:22345407
1315175	Capn15	calpain 15	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210121	MGI			PMID:32885237
1315175	Capn15	calpain 15	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20210121	MGI			PMID:32885237
1315175	Capn15	calpain 15	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20210121	MGI			PMID:32885237
1315175	Capn15	calpain 15	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20210121	MGI			PMID:32885237
1315175	Capn15	calpain 15	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210121	MGI			PMID:32885237
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20241121	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766770
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730198
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469164
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15838507
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730198
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766770
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15838507
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000576	clubfoot		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623520
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623520
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766770
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730198
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20111116	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469164
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730198
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0002073	abnormal hair growth		IEA		N	RGD:5509061	20111116	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20150903	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20260402	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623520
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623520
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0005242	cryptophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0005242	cryptophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766770
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0005242	cryptophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:15838507
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730198
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730198
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20260402	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623520
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0008854	bleb		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469164
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0008854	bleb		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0008856	fetal bleb		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0008856	fetal bleb		IAGP		N	RGD:5509061	20141003	MGI			PMID:15838507
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0009263	abnormal eyelid fusion		IEA		N	RGD:5509061	20260402	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469164
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0009874	abnormal interdigital cell death		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469164
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20150903	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20241121	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0010977	fused right lung lobes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15623520
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766770
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15838507
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766770
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730198
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730198
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12766769
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20260402	MGI			
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0011499	abnormal glomerular capsule space morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730198
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0013177	abnormal tail tip morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:26813283
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0031152	subcutaneous hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:24143185
1315179	Fras1	Fraser extracellular matrix complex subunit 1	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:24143185
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0000561	adactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471509
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666395
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0001677	absent apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0001679	thin apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0004576	abnormal embryonic autopod plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0005109	abnormal talus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471509
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666395
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9733575
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471509
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666395
1315183	Fbxw4	F-box and WD-40 domain protein 4	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:9733575
1315186	Efl1	elongation factor like GTPase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1315186	Efl1	elongation factor like GTPase 1	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20241010	MGI			
1315186	Efl1	elongation factor like GTPase 1	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20241010	MGI			
1315186	Efl1	elongation factor like GTPase 1	gene	MP:0002582	disorganized extraembryonic tissue		IEA		N	RGD:5509061	20241010	MGI			
1315186	Efl1	elongation factor like GTPase 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241010	MGI			
1315186	Efl1	elongation factor like GTPase 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1315186	Efl1	elongation factor like GTPase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315186	Efl1	elongation factor like GTPase 1	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241128	MGI			
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20160324	MGI			PMID:25405900
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20160324	MGI			PMID:25405900
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20160324	MGI			PMID:25405900
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20160324	MGI			PMID:25405900
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20160324	MGI			PMID:25405900
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0005607	decreased bleeding time		IAGP		N	RGD:5509061	20160324	MGI			PMID:25969426
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20160324	MGI			PMID:25405900
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0009586	increased platelet aggregation		IAGP		N	RGD:5509061	20160324	MGI			PMID:25405900
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0009586	increased platelet aggregation		IAGP		N	RGD:5509061	20160324	MGI			PMID:25969426
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0009676	abnormal hemostasis		IAGP		N	RGD:5509061	20160324	MGI			PMID:25969426
1315188	Rgs18	regulator of G-protein signaling 18	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:25969426
1315191	Etv4	ets variant 4	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1315191	Etv4	ets variant 4	gene	MP:0000413	polyphalangy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386269
1315191	Etv4	ets variant 4	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898483
1315191	Etv4	ets variant 4	gene	MP:0000524	decreased renal tubule number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898483
1315191	Etv4	ets variant 4	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386269
1315191	Etv4	ets variant 4	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:14635793
1315191	Etv4	ets variant 4	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372283
1315191	Etv4	ets variant 4	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372283
1315191	Etv4	ets variant 4	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372283
1315191	Etv4	ets variant 4	gene	MP:0000959	abnormal somatic sensory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493690
1315191	Etv4	ets variant 4	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
1315191	Etv4	ets variant 4	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372283
1315191	Etv4	ets variant 4	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:14635793
1315191	Etv4	ets variant 4	gene	MP:0001378	abnormal ejaculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11094084
1315191	Etv4	ets variant 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1315191	Etv4	ets variant 4	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372283
1315191	Etv4	ets variant 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11094084
1315191	Etv4	ets variant 4	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20250508	MGI			
1315191	Etv4	ets variant 4	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898483
1315191	Etv4	ets variant 4	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1315191	Etv4	ets variant 4	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898483
1315191	Etv4	ets variant 4	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898483
1315191	Etv4	ets variant 4	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898483
1315191	Etv4	ets variant 4	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898483
1315191	Etv4	ets variant 4	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898483
1315191	Etv4	ets variant 4	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
1315191	Etv4	ets variant 4	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898483
1315191	Etv4	ets variant 4	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386269
1315191	Etv4	ets variant 4	gene	MP:0008486	decreased muscle spindle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
1315191	Etv4	ets variant 4	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386269
1315191	Etv4	ets variant 4	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20250508	MGI			
1315191	Etv4	ets variant 4	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14635793
1315191	Etv4	ets variant 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386269
1315191	Etv4	ets variant 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386269
1315191	Etv4	ets variant 4	gene	MP:0030996	decreased pacinian corpuscle number		IAGP		N	RGD:5509061	20200130	MGI			PMID:16493690
1315191	Etv4	ets variant 4	gene	MP:0030998	small pacinian corpuscles		IAGP		N	RGD:5509061	20200130	MGI			PMID:16493690
1315193	Mlana	melan-A	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943097
1315193	Mlana	melan-A	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943097
1315193	Mlana	melan-A	gene	MP:0001189	absent skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943097
1315193	Mlana	melan-A	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943097
1315194	Inka2	inka box actin regulator 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:36301793
1315194	Inka2	inka box actin regulator 2	gene	MP:0020337	abnormal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:36301793
1315194	Inka2	inka box actin regulator 2	gene	MP:0021018	decreased dendritic spine number		IAGP		N	RGD:5509061	20230323	MGI			PMID:36301793
1315194	Inka2	inka box actin regulator 2	gene	MP:0021090	abnormal dendrite arborization pattern		IAGP		N	RGD:5509061	20230323	MGI			PMID:36301793
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33524375
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20210617	MGI			PMID:33524375
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20210617	MGI			PMID:33524375
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20210701	MGI			PMID:33524375
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0008903	abnormal mesenteric fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33524375
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210617	MGI			PMID:33524375
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14684813
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0012224	abnormal sterol level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33524375
1315198	Dhcr24	24-dehydrocholesterol reductase	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20150312	MGI			PMID:14684813
1315200	Krt34	keratin 34	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1315200	Krt34	keratin 34	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1315200	Krt34	keratin 34	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1315200	Krt34	keratin 34	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1315200	Krt34	keratin 34	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1315200	Krt34	keratin 34	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1315200	Krt34	keratin 34	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1315200	Krt34	keratin 34	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20241121	MGI			
1315200	Krt34	keratin 34	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1315200	Krt34	keratin 34	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1315200	Krt34	keratin 34	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1315200	Krt34	keratin 34	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20240523	MGI			
1315200	Krt34	keratin 34	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1315202	Ndst4	N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:27793051
1315202	Ndst4	N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:27793051
1315202	Ndst4	N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20180301	MGI			PMID:27793051
1315202	Ndst4	N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4	gene	MP:0014221	increased colon goblet cell number		IAGP		N	RGD:5509061	20180301	MGI			PMID:27793051
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16243035
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16243035
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18334636
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16243035
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18334636
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160908	MGI			PMID:26621702
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20160908	MGI			PMID:26621702
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18334636
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18334636
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18334636
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20160908	MGI			PMID:26621702
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20160908	MGI			PMID:26621702
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20160908	MGI			PMID:26621702
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18334636
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20160908	MGI			PMID:26621702
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18334636
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16243035
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16243035
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16243036
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20160908	MGI			PMID:26621702
1315206	Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:26621702
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20231207	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20241121	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20241121	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20240523	MGI			
1315208	Dcaf5	DDB1 and CUL4 associated factor 5	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20240523	MGI			
1315211	Orai3	ORAI calcium release-activated calcium modulator 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20240516	MGI			PMID:36803766
1315211	Orai3	ORAI calcium release-activated calcium modulator 3	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1315211	Orai3	ORAI calcium release-activated calcium modulator 3	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20240516	MGI			PMID:36803766
1315211	Orai3	ORAI calcium release-activated calcium modulator 3	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20240516	MGI			PMID:36803766
1315211	Orai3	ORAI calcium release-activated calcium modulator 3	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20240516	MGI			PMID:36803766
1315212	Scara5	scavenger receptor class A, member 5	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499552
1315212	Scara5	scavenger receptor class A, member 5	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499552
1315212	Scara5	scavenger receptor class A, member 5	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499552
1315212	Scara5	scavenger receptor class A, member 5	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499552
1315212	Scara5	scavenger receptor class A, member 5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499552
1315212	Scara5	scavenger receptor class A, member 5	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499552
1315212	Scara5	scavenger receptor class A, member 5	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499552
1315212	Scara5	scavenger receptor class A, member 5	gene	MP:0009646	urinary bladder inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499552
1315212	Scara5	scavenger receptor class A, member 5	gene	MP:0020386	adipose tissue inflammation		IAGP		N	RGD:5509061	20161117	MGI			PMID:23499552
1315216	Pik3c2b	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20260806	MGI			PMID:26655903
1315216	Pik3c2b	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20260806	MGI			PMID:26655903
1315216	Pik3c2b	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20260806	MGI			PMID:26655903
1315221	Wdr35	WD repeat domain 35	gene	MP:0000151	absent ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20241121	MGI			
1315221	Wdr35	WD repeat domain 35	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21473986
1315221	Wdr35	WD repeat domain 35	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1315224	Myef2	myelin basic protein expression factor 2, repressor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200514	MGI			
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20201022	MGI			
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20181227	MGI			
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200860
1315226	Stard10	StAR related lipid transfer domain containing 10	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:23200860
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170209	MGI			
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0000445	short snout		IEA		N	RGD:5509061	20170209	MGI			
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0000519	hydronephrosis		IEA		N	RGD:5509061	20170209	MGI			
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592719
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20170209	MGI			
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592719
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0002192	hydrops fetalis		IEA		N	RGD:5509061	20170209	MGI			
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20170209	MGI			
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20170209	MGI			
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592719
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0006130	pulmonary valve atresia		IEA		N	RGD:5509061	20170209	MGI			
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592719
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23592719
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20170209	MGI			
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0010428	abnormal heart right ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0010617	thick mitral valve cusps		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829512
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:23592719
1315228	Dock1	dedicator of cytokinesis 1	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:23592719
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21298075
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:23543054
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:23543054
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21298075
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21298075
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21298075
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20221117	MGI			PMID:23543054
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936227
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0003100	myopia		IAGP		N	RGD:5509061	20221117	MGI			PMID:23543054
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0003986	small cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936227
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936227
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936227
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0004409	abnormal crista ampullaris neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936227
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0004632	abnormal cochlear OHC efferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936227
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0004633	abnormal cochlear IHC efferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936227
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0004746	abnormal cochlear IHC afferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936227
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936227
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21298075
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0011041	abnormal vertical vestibuloocular reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21298075
1315230	Slitrk6	SLIT and NTRK-like family, member 6	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21298075
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20160811	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0000603	pale liver		IEA		N	RGD:5509061	20210520	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20201022	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20181227	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20160811	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0020389	increased radial glial cell number		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315232	Bloc1s2	biogenesis of lysosomal organelles complex-1, subunit 2	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20170518	MGI			PMID:27719760
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0002964	aortic elastic tissue lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0003211	abnormal aorta elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0006083	abnormal blood vessel elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0009869	abnormal descending aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0010903	abnormal pulmonary alveolus wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315234	Slc2a10	solute carrier family 2 (facilitated glucose transporter), member 10	gene	MP:0011309	abnormal kidney arterial blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028722
1315236	Armc5	armadillo repeat containing 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0005129	increased adrenocorticotropin level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0008294	abnormal adrenal gland zona fasciculata morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0008302	thin adrenal cortex		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315236	Armc5	armadillo repeat containing 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180607	MGI			PMID:28911199
1315238	Xpr1	xenotropic and polytropic retrovirus receptor 1	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:2991590
1315241	2900026A02Rik	RIKEN cDNA 2900026A02 gene	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20141003	MGI			
1315241	2900026A02Rik	RIKEN cDNA 2900026A02 gene	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20141003	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514607
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20230119	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22951726
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20231207	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18768888
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514607
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230601	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23034650
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514607
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22951726
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22951726
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20154671
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514607
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22951726
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22951726
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008671	abnormal interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18768888
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22951726
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982598
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008701	abnormal interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18768888
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22951726
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008712	decreased interleukin-9 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20154671
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514607
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1315247	Il17ra	interleukin 17 receptor A	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22951726
1315249	Rem1	rad and gem related GTP binding protein 1	gene	MP:0020346	abnormal myocardial fiber calcium currents		IAGP		N	RGD:5509061	20230223	MGI			PMID:22854599
1315253	Ftmt	ferritin mitochondrial	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0000333	decreased bone marrow cell number		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0000743	muscle spasm		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0000746	weakness		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357897
1315255	Dst	dystonin	gene	MP:0000754	paresis		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0000911	abnormal trigeminal motor nucleus morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:3138544
1315255	Dst	dystonin	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9570777
1315255	Dst	dystonin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12859670
1315255	Dst	dystonin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7217981
1315255	Dst	dystonin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9570777
1315255	Dst	dystonin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618216
1315255	Dst	dystonin	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0000958	peripheral nervous system degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581287
1315255	Dst	dystonin	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12859670
1315255	Dst	dystonin	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618216
1315255	Dst	dystonin	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581287
1315255	Dst	dystonin	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289886
1315255	Dst	dystonin	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289886
1315255	Dst	dystonin	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9570777
1315255	Dst	dystonin	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1315255	Dst	dystonin	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0001408	stereotypic behavior		IEA		N	RGD:5509061	20150402	MGI			
1315255	Dst	dystonin	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:133598
1315255	Dst	dystonin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:133598
1315255	Dst	dystonin	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:3138544
1315255	Dst	dystonin	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0001527	athetotic walking movements		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1315255	Dst	dystonin	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0002064	seizures		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:3138544
1315255	Dst	dystonin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:133598
1315255	Dst	dystonin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357897
1315255	Dst	dystonin	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:4655279
1315255	Dst	dystonin	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:133598
1315255	Dst	dystonin	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:4655279
1315255	Dst	dystonin	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12859670
1315255	Dst	dystonin	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12859670
1315255	Dst	dystonin	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357897
1315255	Dst	dystonin	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7374955
1315255	Dst	dystonin	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0002883	chromatolysis		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1315255	Dst	dystonin	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357897
1315255	Dst	dystonin	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:1634998
1315255	Dst	dystonin	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:4655279
1315255	Dst	dystonin	gene	MP:0003280	urinary incontinence		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0003281	fecal incontinence		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:4655279
1315255	Dst	dystonin	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12859670
1315255	Dst	dystonin	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9570777
1315255	Dst	dystonin	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9570777
1315255	Dst	dystonin	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3138544
1315255	Dst	dystonin	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581287
1315255	Dst	dystonin	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618216
1315255	Dst	dystonin	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357897
1315255	Dst	dystonin	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:12859670
1315255	Dst	dystonin	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0005150	cachexia		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0005191	head tilt		IEA		N	RGD:5509061	20150402	MGI			
1315255	Dst	dystonin	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0005316	abnormal response to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:133598
1315255	Dst	dystonin	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0005356	positive geotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12859670
1315255	Dst	dystonin	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9570777
1315255	Dst	dystonin	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12859670
1315255	Dst	dystonin	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7736575
1315255	Dst	dystonin	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618216
1315255	Dst	dystonin	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087202
1315255	Dst	dystonin	gene	MP:0006258	abnormal circumvallate papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289886
1315255	Dst	dystonin	gene	MP:0006260	abnormal gustatory papilla taste bud morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:16289886
1315255	Dst	dystonin	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381311
1315255	Dst	dystonin	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0009400	decreased skeletal muscle fiber size		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1315255	Dst	dystonin	gene	MP:0011085	postnatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1315255	Dst	dystonin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315255	Dst	dystonin	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20160304	MGI			PMID:25195653
1315255	Dst	dystonin	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20180628	MGI			PMID:27693510
1315255	Dst	dystonin	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:10357897
1315260	Mtmr1	myotubularin related protein 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1315260	Mtmr1	myotubularin related protein 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1315260	Mtmr1	myotubularin related protein 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1315260	Mtmr1	myotubularin related protein 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21479251
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21479251
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0006428	ectopic Sertoli cells		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21479251
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0014684	impaired spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0020356	abnormal Sertoli cell barrier function		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315262	Kpna6	karyopherin subunit alpha 6	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220721	MGI			PMID:34473250
1315265	Anapc4	anaphase promoting complex subunit 4	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20240829	MGI			PMID:38932933
1315265	Anapc4	anaphase promoting complex subunit 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315265	Anapc4	anaphase promoting complex subunit 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1315265	Anapc4	anaphase promoting complex subunit 4	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1315267	Exosc2	exosome component 2	gene	MP:0001714	absent trophoblast giant cells		IAGP		N	RGD:5509061	20240104	MGI			PMID:37940010
1315267	Exosc2	exosome component 2	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20240104	MGI			PMID:37940010
1315267	Exosc2	exosome component 2	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20240104	MGI			PMID:37940010
1315267	Exosc2	exosome component 2	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20240104	MGI			PMID:37940010
1315267	Exosc2	exosome component 2	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20240104	MGI			PMID:37940010
1315267	Exosc2	exosome component 2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20240104	MGI			PMID:37940010
1315267	Exosc2	exosome component 2	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20240104	MGI			PMID:37940010
1315267	Exosc2	exosome component 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315267	Exosc2	exosome component 2	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20240104	MGI			PMID:37940010
1315267	Exosc2	exosome component 2	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20240104	MGI			PMID:37940010
1315267	Exosc2	exosome component 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1315267	Exosc2	exosome component 2	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240926	MGI			PMID:37940010
1315269	Rfx1	regulatory factor X, 1 (influences HLA class II expression)	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1315269	Rfx1	regulatory factor X, 1 (influences HLA class II expression)	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1315269	Rfx1	regulatory factor X, 1 (influences HLA class II expression)	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1315269	Rfx1	regulatory factor X, 1 (influences HLA class II expression)	gene	MP:0004403	absent cochlear outer hair cells		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1315269	Rfx1	regulatory factor X, 1 (influences HLA class II expression)	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1315269	Rfx1	regulatory factor X, 1 (influences HLA class II expression)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1315269	Rfx1	regulatory factor X, 1 (influences HLA class II expression)	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1315269	Rfx1	regulatory factor X, 1 (influences HLA class II expression)	gene	MP:0011061	abnormal inner hair cell kinocilium morphology		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1315269	Rfx1	regulatory factor X, 1 (influences HLA class II expression)	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19559676
1315271	Lrpprc	leucine-rich PPR-motif containing	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:22045337
1315271	Lrpprc	leucine-rich PPR-motif containing	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22045337
1315271	Lrpprc	leucine-rich PPR-motif containing	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21880015
1315271	Lrpprc	leucine-rich PPR-motif containing	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1315271	Lrpprc	leucine-rich PPR-motif containing	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22045337
1315271	Lrpprc	leucine-rich PPR-motif containing	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21880015
1315271	Lrpprc	leucine-rich PPR-motif containing	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22045337
1315271	Lrpprc	leucine-rich PPR-motif containing	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22045337
1315271	Lrpprc	leucine-rich PPR-motif containing	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20190711	MGI			PMID:22045337
1315274	Faf2	Fas associated factor family member 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161110	MGI			PMID:25970332
1315274	Faf2	Fas associated factor family member 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20201022	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20210128	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20201022	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210128	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20161110	MGI			PMID:25970332
1315274	Faf2	Fas associated factor family member 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20161110	MGI			PMID:25970332
1315274	Faf2	Fas associated factor family member 2	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20201022	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20161110	MGI			PMID:25970332
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20230601	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210128	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20210128	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20201022	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20210128	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20210128	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20161110	MGI			PMID:25970332
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20161110	MGI			PMID:25970332
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003981	decreased circulating phospholipid level		IAGP		N	RGD:5509061	20161110	MGI			PMID:25970332
1315274	Faf2	Fas associated factor family member 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20161110	MGI			PMID:25970332
1315274	Faf2	Fas associated factor family member 2	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20201022	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0010331	abnormal apolipoprotein level		IAGP		N	RGD:5509061	20161110	MGI			PMID:25970332
1315274	Faf2	Fas associated factor family member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315274	Faf2	Fas associated factor family member 2	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:25970332
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170330	MGI			PMID:25843235
1315281	Ntmt1	N-terminal Xaa-Pro-Lys N-methyltransferase 1	gene	MP:0014273	abnormal skin vasculature morphology		IAGP		N	RGD:5509061	20230810	MGI			PMID:25843235
1315288	Pkdrej	polycystin (PKD) family receptor for egg jelly	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1315288	Pkdrej	polycystin (PKD) family receptor for egg jelly	gene	MP:0003666	impaired sperm capacitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18562295
1315292	Gca	grancalcin	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529388
1315294	Agfg2	ArfGAP with FG repeats 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20231207	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20231207	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160811	MGI			PMID:27122027
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315296	Tmem184b	transmembrane protein 184b	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
1315299	Zdhhc12	zinc finger, DHHC domain containing 12	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20260122	MGI			PMID:36586411
1315299	Zdhhc12	zinc finger, DHHC domain containing 12	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20260122	MGI			PMID:36586411
1315299	Zdhhc12	zinc finger, DHHC domain containing 12	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20260122	MGI			PMID:36586411
1315299	Zdhhc12	zinc finger, DHHC domain containing 12	gene	MP:0014437	increased interleukin level		IAGP		N	RGD:5509061	20260122	MGI			PMID:36586411
1315299	Zdhhc12	zinc finger, DHHC domain containing 12	gene	MP:0014787	increased protein level		IAGP		N	RGD:5509061	20260122	MGI			PMID:36586411
1315302	Oscp1	organic solute carrier partner 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20181227	MGI			
1315304	Cyc1	cytochrome c-1	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20241010	MGI			
1315304	Cyc1	cytochrome c-1	gene	MP:0003886	abnormal embryonic epiblast morphology		IEA		N	RGD:5509061	20241010	MGI			
1315304	Cyc1	cytochrome c-1	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IEA		N	RGD:5509061	20241010	MGI			
1315304	Cyc1	cytochrome c-1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241010	MGI			
1315304	Cyc1	cytochrome c-1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1315304	Cyc1	cytochrome c-1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0000267	abnormal heart development		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0000928	incomplete rostral neuropore closure		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0003400	kinked neural tube		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20241121	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0012099	decreased spongiotrophoblast size		IEA		N	RGD:5509061	20251211	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1315308	Urm1	ubiquitin related modifier 1	gene	MP:0014134	abnormal embryo morphology		IEA		N	RGD:5509061	20251211	MGI			
1315315	Cyp46a1	cytochrome P450, family 46, subfamily a, polypeptide 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12686551
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210826	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201022	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20230601	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20210826	MGI			
1315317	Eppin	epididymal peptidase inhibitor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1315319	Trip12	thyroid hormone receptor interactor 12	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22028794
1315319	Trip12	thyroid hormone receptor interactor 12	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22028794
1315319	Trip12	thyroid hormone receptor interactor 12	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:23747016
1315319	Trip12	thyroid hormone receptor interactor 12	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22028794
1315319	Trip12	thyroid hormone receptor interactor 12	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20260813	MGI			PMID:42310454
1315319	Trip12	thyroid hormone receptor interactor 12	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23747016
1315319	Trip12	thyroid hormone receptor interactor 12	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22028794
1315319	Trip12	thyroid hormone receptor interactor 12	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20260813	MGI			PMID:42310454
1315324	Otog	otogelin	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0001967	deafness		IEA		N	RGD:5509061	20111116	MGI			
1315324	Otog	otogelin	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20240523	MGI			
1315324	Otog	otogelin	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0002894	abnormal otolith morphology		IEA		N	RGD:5509061	20111116	MGI			
1315324	Otog	otogelin	gene	MP:0002895	abnormal otolithic membrane morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0003145	detached otolithic membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0003145	detached otolithic membrane		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0003878	abnormal ear physiology		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0004330	abnormal vestibular saccular macula morphology		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0004517	decreased vestibular hair cell stereocilia number		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1315324	Otog	otogelin	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1315324	Otog	otogelin	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0006328	nonsyndromic hearing impairment		IAGP		N	RGD:5509061	20170427	MGI			PMID:26636018
1315324	Otog	otogelin	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315324	Otog	otogelin	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1315324	Otog	otogelin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315324	Otog	otogelin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655058
1315324	Otog	otogelin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20220407	MGI			PMID:11178734
1315328	Ca12	carbonic anhydrase 12	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16800892
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20260402	MGI			
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315330	Yae1d1	Yae1 domain containing 1	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1315331	Ubfd1	ubiquitin family domain containing 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1315331	Ubfd1	ubiquitin family domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1315335	Mcm5	minichromosome maintenance complex component 5	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141003	MGI			
1315337	Sptlc1	serine palmitoyltransferase, long chain base subunit 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16216550
1315337	Sptlc1	serine palmitoyltransferase, long chain base subunit 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1315337	Sptlc1	serine palmitoyltransferase, long chain base subunit 1	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16216550
1315337	Sptlc1	serine palmitoyltransferase, long chain base subunit 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1315337	Sptlc1	serine palmitoyltransferase, long chain base subunit 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16216550
1315337	Sptlc1	serine palmitoyltransferase, long chain base subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315339	Prnd	prion like protein doppel	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161660
1315339	Prnd	prion like protein doppel	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12110578
1315339	Prnd	prion like protein doppel	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15007175
1315339	Prnd	prion like protein doppel	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161660
1315339	Prnd	prion like protein doppel	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12110578
1315339	Prnd	prion like protein doppel	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12110578
1315339	Prnd	prion like protein doppel	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12110578
1315339	Prnd	prion like protein doppel	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161660
1315339	Prnd	prion like protein doppel	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12110578
1315339	Prnd	prion like protein doppel	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15007175
1315339	Prnd	prion like protein doppel	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12110578
1315339	Prnd	prion like protein doppel	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12110578
1315339	Prnd	prion like protein doppel	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12110578
1315339	Prnd	prion like protein doppel	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20191017	MGI			PMID:12110578
1315341	Cbx5	chromobox 5	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20141003	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20150430	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20150430	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763435
1315341	Cbx5	chromobox 5	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141003	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0009456	impaired cued conditioning behavior		IEA		N	RGD:5509061	20260402	MGI			
1315341	Cbx5	chromobox 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22670227
1315341	Cbx5	chromobox 5	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20260402	MGI			
1315343	Map2k3	mitogen-activated protein kinase kinase 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723219
1315343	Map2k3	mitogen-activated protein kinase kinase 3	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151339
1315343	Map2k3	mitogen-activated protein kinase kinase 3	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151339
1315343	Map2k3	mitogen-activated protein kinase kinase 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723219
1315347	Carmil1	capping protein regulator and myosin 1 linker 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0001440	abnormal grooming behavior		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20220811	MGI			
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0008462	abnormal medium spiny neuron morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0013894	abnormal behavioral response to amphetamine		IAGP		N	RGD:5509061	20180607	MGI			PMID:28433741
1315348	Zswim6	zinc finger SWIM-type containing 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:28433741
1315349	Smim23	small integral membrane protein 23	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20201022	MGI			
1315349	Smim23	small integral membrane protein 23	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1315349	Smim23	small integral membrane protein 23	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20201022	MGI			
1315350	Tmbim7	transmembrane BAX inhibitor motif containing 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0009500	abnormal interlobular bile duct morphology		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0009837	abnormal sperm end piece morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20230302	MGI			PMID:30423168
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0014631	abnormal elongated spermatid morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0031351	abnormal sperm flagellum thickness		IAGP		N	RGD:5509061	20220317	MGI			PMID:34023333
1315353	Lztfl1	leucine zipper transcription factor-like 1	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:26216965
1315354	Anapc1	anaphase promoting complex subunit 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1315354	Anapc1	anaphase promoting complex subunit 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1315354	Anapc1	anaphase promoting complex subunit 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1315354	Anapc1	anaphase promoting complex subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315354	Anapc1	anaphase promoting complex subunit 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1315358	Deup1	deuterosome assembly protein 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1315358	Deup1	deuterosome assembly protein 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20231207	MGI			
1315358	Deup1	deuterosome assembly protein 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210520	MGI			
1315358	Deup1	deuterosome assembly protein 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20231207	MGI			
1315358	Deup1	deuterosome assembly protein 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1315358	Deup1	deuterosome assembly protein 1	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1315358	Deup1	deuterosome assembly protein 1	gene	MP:0010152	abnormal brain ependyma morphology		IAGP		N	RGD:5509061	20251127	MGI			PMID:31792378
1315358	Deup1	deuterosome assembly protein 1	gene	MP:0014239	abnormal intracellular organelle morphology		IAGP		N	RGD:5509061	20251127	MGI			PMID:31792378
1315358	Deup1	deuterosome assembly protein 1	gene	MP:0014241	abnormal intracellular organelle physiology		IAGP		N	RGD:5509061	20251127	MGI			PMID:31792378
1315359	Zfp39	zinc finger protein 39	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20250508	MGI			
1315359	Zfp39	zinc finger protein 39	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20250508	MGI			
1315359	Zfp39	zinc finger protein 39	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20250508	MGI			
1315359	Zfp39	zinc finger protein 39	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20200514	MGI			
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0003617	urinary bladder hypoplasia		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0011923	abnormal bladder urine volume		IAGP		N	RGD:5509061	20180920	MGI			PMID:29432158
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0012462	decreased brain internal capsule size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0012474	decreased cingulate cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0012477	increased secondary somatosensory cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0012482	decreased habenula size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1315361	Maz	MYC-associated zinc finger protein (purine-binding transcription factor)	gene	MP:0013908	small lateral ventricles		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1315362	Mrfap1	Morf4 family associated protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367658
1315363	Asphd1	aspartate beta-hydroxylase domain containing 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1315363	Asphd1	aspartate beta-hydroxylase domain containing 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1315363	Asphd1	aspartate beta-hydroxylase domain containing 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1315363	Asphd1	aspartate beta-hydroxylase domain containing 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1315363	Asphd1	aspartate beta-hydroxylase domain containing 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230601	MGI			
1315363	Asphd1	aspartate beta-hydroxylase domain containing 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20230601	MGI			
1315363	Asphd1	aspartate beta-hydroxylase domain containing 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1315363	Asphd1	aspartate beta-hydroxylase domain containing 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20230601	MGI			
1315365	Atxn2	ataxin 2	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293225
1315365	Atxn2	ataxin 2	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22956915
1315365	Atxn2	ataxin 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293225
1315365	Atxn2	ataxin 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22956915
1315365	Atxn2	ataxin 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293225
1315365	Atxn2	ataxin 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22956915
1315365	Atxn2	ataxin 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293225
1315365	Atxn2	ataxin 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0002997	enlarged seminal vesicle		IAGP		N	RGD:5509061	20141204	MGI			PMID:16293225
1315365	Atxn2	ataxin 2	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0005415	intrahepatic cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293225
1315365	Atxn2	ataxin 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20150611	MGI			PMID:18250099
1315365	Atxn2	ataxin 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250099
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862711
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862711
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862711
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862711
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20171109	MGI			PMID:23695275
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20171109	MGI			PMID:23695275
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0003024	coronary artery stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20171109	MGI			PMID:23695275
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:23695275
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20171109	MGI			PMID:23695275
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862711
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862711
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20231221	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0009416	cardiac muscle degeneration		IAGP		N	RGD:5509061	20171109	MGI			PMID:23695275
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862711
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0010394	decreased QRS amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:10481911
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:23695275
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20171109	MGI			PMID:23695275
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0011749	perivascular fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862711
1315367	Sgcd	sarcoglycan, delta (dystrophin-associated glycoprotein)	gene	MP:0012735	abnormal response to exercise		IAGP		N	RGD:5509061	20171109	MGI			PMID:23695275
1315372	Tenm3	teneurin transmembrane protein 3	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803360
1315372	Tenm3	teneurin transmembrane protein 3	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803360
1315372	Tenm3	teneurin transmembrane protein 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803360
1315372	Tenm3	teneurin transmembrane protein 3	gene	MP:0030831	abnormal glenoid fossa morphology		IAGP		N	RGD:5509061	20251127	MGI			PMID:30273960
1315372	Tenm3	teneurin transmembrane protein 3	gene	MP:0030838	abnormal acetabular fossa morphology		IAGP		N	RGD:5509061	20251127	MGI			PMID:30273960
1315375	Fam120a	family with sequence similarity 120, member A	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1315375	Fam120a	family with sequence similarity 120, member A	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1315375	Fam120a	family with sequence similarity 120, member A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1315375	Fam120a	family with sequence similarity 120, member A	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1315375	Fam120a	family with sequence similarity 120, member A	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220519	MGI			
1315375	Fam120a	family with sequence similarity 120, member A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1315375	Fam120a	family with sequence similarity 120, member A	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1315375	Fam120a	family with sequence similarity 120, member A	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1315375	Fam120a	family with sequence similarity 120, member A	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20190411	MGI			PMID:28627522
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159644
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:28627522
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20190411	MGI			PMID:28627522
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:28627522
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21741597
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0010506	prolonged RR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0010559	heart block		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285465
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159644
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289070
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:18787701
1315377	Dot1l	DOT1 like histone lysine methyltransferase	gene	MP:0030928	increased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:18787701
1315378	Znrf1	zinc and ring finger 1	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28593998
1315378	Znrf1	zinc and ring finger 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20191114	MGI			PMID:28593998
1315383	Spryd4	SPRY domain containing 4	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1315383	Spryd4	SPRY domain containing 4	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20201022	MGI			
1315383	Spryd4	SPRY domain containing 4	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20201022	MGI			
1315383	Spryd4	SPRY domain containing 4	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20201022	MGI			
1315383	Spryd4	SPRY domain containing 4	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1315385	Lamc2	laminin, gamma 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14632187
1315385	Lamc2	laminin, gamma 2	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14632187
1315385	Lamc2	laminin, gamma 2	gene	MP:0000578	ulcerated autopod		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0000578	ulcerated autopod		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20170209	MGI			PMID:14632187
1315385	Lamc2	laminin, gamma 2	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20170209	MGI			PMID:14632187
1315385	Lamc2	laminin, gamma 2	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14632187
1315385	Lamc2	laminin, gamma 2	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240829	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14632187
1315385	Lamc2	laminin, gamma 2	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20170209	MGI			PMID:22507638
1315385	Lamc2	laminin, gamma 2	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0004273	abnormal basal lamina morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0005275	abnormal skin tensile strength		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0009827	skin detachment		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0009827	skin detachment		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0010936	decreased airway resistance		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0011045	decreased lung elastance		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:14632187
1315385	Lamc2	laminin, gamma 2	gene	MP:0011159	abnormal epidermal-dermal junction morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22507638
1315385	Lamc2	laminin, gamma 2	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20170209	MGI			PMID:14632187
1315385	Lamc2	laminin, gamma 2	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20170209	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20170209	MGI			PMID:22507638
1315385	Lamc2	laminin, gamma 2	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0012400	nail dystrophy		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0012402	abnormal nail bed morphology		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1315385	Lamc2	laminin, gamma 2	gene	MP:0030423	abnormal pinna cartilage morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:20336083
1315385	Lamc2	laminin, gamma 2	gene	MP:0030460	enamel pits		IAGP		N	RGD:5509061	20171221	MGI			PMID:20336083
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632078
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1315388	Prss16	serine protease 16 (thymus)	gene	MP:0008195	abnormal professional antigen presenting cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19283781
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995385
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995385
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995385
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0008007	abnormal cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995385
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:16476774
1315391	Bub3	BUB3 mitotic checkpoint protein	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:10995385
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20250508	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20170105	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20141003	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160804	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20141003	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20250508	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0006415	absent testes		IEA		N	RGD:5509061	20250508	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20250508	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1315393	Arvcf	armadillo repeat gene deleted in velocardiofacial syndrome	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1315394	Inca1	inhibitor of CDK, cyclin A1 interacting protein 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540187
1315394	Inca1	inhibitor of CDK, cyclin A1 interacting protein 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540187
1315394	Inca1	inhibitor of CDK, cyclin A1 interacting protein 1	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540187
1315394	Inca1	inhibitor of CDK, cyclin A1 interacting protein 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540187
1315394	Inca1	inhibitor of CDK, cyclin A1 interacting protein 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540187
1315394	Inca1	inhibitor of CDK, cyclin A1 interacting protein 1	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540187
1315394	Inca1	inhibitor of CDK, cyclin A1 interacting protein 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21540187
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230601	MGI			
1315396	Usp32	ubiquitin specific peptidase 32	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000098	abnormal vomer bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001230	epidermal desquamation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11053261
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001310	abnormal conjunctiva morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11053261
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11053261
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20241121	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747812
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20231130	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002691	small stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20150319	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231695
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366192
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004379	wide frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004546	esophagus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004574	broad limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004657	small sacral vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004882	enlarged lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11053261
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11053261
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14960276
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366192
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005415	intrahepatic cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747812
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008717	increased lung squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231695
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231695
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0008991	abnormal bile canaliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009343	dilated gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747812
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747812
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20150319	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20170309	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0010234	abnormal vibrissa follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14960276
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0010799	stomach mucosa hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0010864	abnormal enamel knot morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:14960276
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0010880	small esophagus		IAGP		N	RGD:5509061	20150319	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772111
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195895
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351639
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011706	abnormal fibroblast migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231695
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20170223	MGI			PMID:20231695
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0012279	wide sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20230119	MGI			
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0013182	increased spinal cord apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10898787
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0020416	decreased fibroblast chemotaxis		IAGP		N	RGD:5509061	20170223	MGI			PMID:20231695
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0020859	disorganized cornea epithelium		IAGP		N	RGD:5509061	20181101	MGI			PMID:11053261
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0030079	small incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:10346820
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0030197	small nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0030266	small vomer bone		IAGP		N	RGD:5509061	20171026	MGI			PMID:10195896
1315402	Chuk	conserved helix-loop-helix ubiquitous kinase	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:14960276
1315407	Fbxo22	F-box protein 22	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20210128	MGI			
1315407	Fbxo22	F-box protein 22	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1315407	Fbxo22	F-box protein 22	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1315407	Fbxo22	F-box protein 22	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20181227	MGI			
1315407	Fbxo22	F-box protein 22	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20230831	MGI			PMID:26868148
1315407	Fbxo22	F-box protein 22	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1315407	Fbxo22	F-box protein 22	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1315407	Fbxo22	F-box protein 22	gene	MP:0010580	decreased heart left ventricle size		IEA		N	RGD:5509061	20210128	MGI			
1315407	Fbxo22	F-box protein 22	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230831	MGI			PMID:26868148
1315407	Fbxo22	F-box protein 22	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20230831	MGI			PMID:26868148
1315409	Tle2	transducin-like enhancer of split 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
1315409	Tle2	transducin-like enhancer of split 2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
1315409	Tle2	transducin-like enhancer of split 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20250220	MGI			PMID:33658226
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482799
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20592205
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482799
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482799
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:20592205
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0011392	increased fetal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315411	Ppp2r5d	protein phosphatase 2, regulatory subunit B', delta	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1315412	Prss34	serine protease 34	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20211202	MGI			PMID:27789480
1315412	Prss34	serine protease 34	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20211202	MGI			PMID:27789480
1315414	Fis1	fission, mitochondrial 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20210916	MGI			PMID:34355730
1315414	Fis1	fission, mitochondrial 1	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20210916	MGI			PMID:34355730
1315414	Fis1	fission, mitochondrial 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20210916	MGI			PMID:34355730
1315414	Fis1	fission, mitochondrial 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20210128	MGI			
1315414	Fis1	fission, mitochondrial 1	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20210916	MGI			PMID:34355730
1315414	Fis1	fission, mitochondrial 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0008608	increased circulating interleukin-13 level		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0008647	increased circulating interleukin-12b level		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315414	Fis1	fission, mitochondrial 1	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20210916	MGI			PMID:34355730
1315414	Fis1	fission, mitochondrial 1	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20200806	MGI			PMID:31526891
1315414	Fis1	fission, mitochondrial 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20210916	MGI			PMID:34355730
1315414	Fis1	fission, mitochondrial 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20210916	MGI			PMID:34355730
1315414	Fis1	fission, mitochondrial 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20210916	MGI			PMID:34355730
1315416	Arhgap24	Rho GTPase activating protein 24	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20201022	MGI			
1315416	Arhgap24	Rho GTPase activating protein 24	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20210128	MGI			
1315416	Arhgap24	Rho GTPase activating protein 24	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20200402	MGI			
1315420	Med4	mediator complex subunit 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1315420	Med4	mediator complex subunit 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:12947200
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:12947200
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12947200
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12947200
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:28196692
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0004806	absent germ cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12947200
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12947200
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20190919	MGI			PMID:28196692
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12947200
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20240530	MGI			PMID:38325858
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281459
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0006361	abnormal female germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281459
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38325858
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12947200
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:28196692
1315422	Nanos3	nanos C2HC-type zinc finger 3	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0014397	increased fat cell mitochondrial DNA content		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0014398	abnormal fat cell mitochondrial morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1315428	Rbm43	RNA binding motif protein 43	gene	MP:0014911	increased fat cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:39965564
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0001023	L5 dorsal root ganglion hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315430	Dock3	dedicator of cyto-kinesis 3	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129390
1315432	Brdt	bromodomain, testis-specific	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728347
1315432	Brdt	bromodomain, testis-specific	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:17728347
1315432	Brdt	bromodomain, testis-specific	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:17728347
1315432	Brdt	bromodomain, testis-specific	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0004647	decreased lumbar vertebrae number		IEA		N	RGD:5509061	20141003	MGI			
1315432	Brdt	bromodomain, testis-specific	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:17728347
1315432	Brdt	bromodomain, testis-specific	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728347
1315432	Brdt	bromodomain, testis-specific	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922464
1315432	Brdt	bromodomain, testis-specific	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:17728347
1315432	Brdt	bromodomain, testis-specific	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:17728347
1315432	Brdt	bromodomain, testis-specific	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:17728347
1315432	Brdt	bromodomain, testis-specific	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20141003	MGI			
1315432	Brdt	bromodomain, testis-specific	gene	MP:0013330	abnormal male accessory sex gland morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20160915	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:26994494
1315432	Brdt	bromodomain, testis-specific	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220714	MGI			PMID:17728347
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20180426	MGI			PMID:28552356
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20201022	MGI			
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20240523	MGI			
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20221215	MGI			
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0003760	decreased palatal length		IAGP		N	RGD:5509061	20180426	MGI			PMID:28552356
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201022	MGI			
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180308	MGI			PMID:28422762
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20221215	MGI			
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1315437	Smoc2	SPARC related modular calcium binding 2	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20180426	MGI			PMID:28552356
1315442	Spaca3	sperm acrosome associated 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1315445	Mrpl51	mitochondrial ribosomal protein L51	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1315445	Mrpl51	mitochondrial ribosomal protein L51	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315445	Mrpl51	mitochondrial ribosomal protein L51	gene	MP:0011435	increased urine magnesium level		IEA		N	RGD:5509061	20210128	MGI			
1315445	Mrpl51	mitochondrial ribosomal protein L51	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1315445	Mrpl51	mitochondrial ribosomal protein L51	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1315447	Noxa1	NADPH oxidase activator 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20241121	MGI			
1315447	Noxa1	NADPH oxidase activator 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20241121	MGI			
1315447	Noxa1	NADPH oxidase activator 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20241121	MGI			
1315447	Noxa1	NADPH oxidase activator 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20645308
1315447	Noxa1	NADPH oxidase activator 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1315447	Noxa1	NADPH oxidase activator 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20241121	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20220519	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20210826	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210826	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21170927
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20220519	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20210826	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1315451	Mllt6	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20181227	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0000371	diluted coat color		IEA		N	RGD:5509061	20111116	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9864865
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9864865
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20111116	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0001924	infertility		IEA		N	RGD:5509061	20111116	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238537
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0002095	abnormal skin pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0005172	decreased eye pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0005408	hypopigmentation		IEA		N	RGD:5509061	20111116	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0008480	absent eye pigmentation		IEA		N	RGD:5509061	20141003	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0009928	abnormal pinna hair pigmentation		IEA		N	RGD:5509061	20141003	MGI			
1315453	Slc45a2	solute carrier family 45, member 2	gene	MP:0011627	decreased skin pigmentation		IEA		N	RGD:5509061	20141003	MGI			
1315456	Serpinf2	serine (or cysteine) peptidase inhibitor, clade F, member 2	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10090937
1315456	Serpinf2	serine (or cysteine) peptidase inhibitor, clade F, member 2	gene	MP:0003422	abnormal thrombolysis		IAGP		N	RGD:5509061	20201001	MGI			PMID:10090937
1315456	Serpinf2	serine (or cysteine) peptidase inhibitor, clade F, member 2	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20201001	MGI			PMID:10318667
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16824198
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12356737
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0003223	decreased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16824198
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20230601	MGI			
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:16824198
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20230601	MGI			
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16824198
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315458	Bach1	BTB and CNC homology 1, basic leucine zipper transcription factor 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22974978
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264090
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22974978
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264090
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22974978
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20150305	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22974978
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264090
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0002635	reduced sensorimotor gating		IAGP		N	RGD:5509061	20150305	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:22974978
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264090
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0002801	abnormal long-term object recognition memory		IAGP		N	RGD:5509061	20150305	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20150305	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22974978
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264090
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20150305	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20150305	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0009949	abnormal olfactory bulb granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0009952	abnormal olfactory bulb subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21632933
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22974978
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20150305	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20150305	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:25378165
1315459	Ccdc88a	coiled coil domain containing 88A	gene	MP:0030956	abnormal neuronal precursor cell migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:21632933
1315461	Pltp	phospholipid transfer protein	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079112
1315461	Pltp	phospholipid transfer protein	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079112
1315461	Pltp	phospholipid transfer protein	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079112
1315461	Pltp	phospholipid transfer protein	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20170629	MGI			PMID:23846500
1315461	Pltp	phospholipid transfer protein	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467369
1315461	Pltp	phospholipid transfer protein	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514421
1315461	Pltp	phospholipid transfer protein	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514421
1315461	Pltp	phospholipid transfer protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467369
1315461	Pltp	phospholipid transfer protein	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20170629	MGI			PMID:23846500
1315461	Pltp	phospholipid transfer protein	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467369
1315461	Pltp	phospholipid transfer protein	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467369
1315461	Pltp	phospholipid transfer protein	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467369
1315461	Pltp	phospholipid transfer protein	gene	MP:0003191	abnormal cellular cholesterol metabolism		IAGP		N	RGD:5509061	20170629	MGI			PMID:23846500
1315461	Pltp	phospholipid transfer protein	gene	MP:0003981	decreased circulating phospholipid level		IAGP		N	RGD:5509061	20170629	MGI			PMID:23846500
1315461	Pltp	phospholipid transfer protein	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467369
1315461	Pltp	phospholipid transfer protein	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079112
1315461	Pltp	phospholipid transfer protein	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079112
1315461	Pltp	phospholipid transfer protein	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20170629	MGI			PMID:23846500
1315461	Pltp	phospholipid transfer protein	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514421
1315461	Pltp	phospholipid transfer protein	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514421
1315461	Pltp	phospholipid transfer protein	gene	MP:0011231	abnormal vitamin E level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467369
1315461	Pltp	phospholipid transfer protein	gene	MP:0020126	decreased circulating HDL phospholipid level		IAGP		N	RGD:5509061	20170629	MGI			PMID:23846500
1315461	Pltp	phospholipid transfer protein	gene	MP:0020129	decreased circulating non-HDL phospholipid level		IAGP		N	RGD:5509061	20170629	MGI			PMID:23846500
1315461	Pltp	phospholipid transfer protein	gene	MP:0020151	abnormal circulating non-HDL cholesterol level		IAGP		N	RGD:5509061	20170629	MGI			PMID:23846500
1315461	Pltp	phospholipid transfer protein	gene	MP:0020854	increased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:21514421
1315461	Pltp	phospholipid transfer protein	gene	MP:0020859	disorganized cornea epithelium		IAGP		N	RGD:5509061	20181101	MGI			PMID:21514421
1315461	Pltp	phospholipid transfer protein	gene	MP:0031432	cornea perforation		IAGP		N	RGD:5509061	20220721	MGI			PMID:21514421
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576088
1315463	Abcc10	ATP-binding cassette, sub-family C member 10	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1315464	Wdr91	WD repeat domain 91	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220519	MGI			
1315464	Wdr91	WD repeat domain 91	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20191114	MGI			PMID:28860274
1315464	Wdr91	WD repeat domain 91	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001573	abnormal circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077570
1315465	Mcat	malonyl CoA:ACP acyltransferase (mitochondrial)	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:23077570
1315467	Fhod1	formin homology 2 domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201001	MGI			PMID:31008549
1315467	Fhod1	formin homology 2 domain containing 1	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1315467	Fhod1	formin homology 2 domain containing 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220519	MGI			
1315467	Fhod1	formin homology 2 domain containing 1	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20210826	MGI			
1315469	Zfp385a	zinc finger protein 385A	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927637
1315469	Zfp385a	zinc finger protein 385A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927637
1315469	Zfp385a	zinc finger protein 385A	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927637
1315469	Zfp385a	zinc finger protein 385A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10585558
1315469	Zfp385a	zinc finger protein 385A	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927637
1315469	Zfp385a	zinc finger protein 385A	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927637
1315469	Zfp385a	zinc finger protein 385A	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927637
1315469	Zfp385a	zinc finger protein 385A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927637
1315469	Zfp385a	zinc finger protein 385A	gene	MP:0020431	decreased platelet alpha-granule number		IAGP		N	RGD:5509061	20170803	MGI			PMID:11927637
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001924	infertility		IEA		N	RGD:5509061	20141003	MGI			
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230601	MGI			
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0002102	abnormal ear morphology		IEA		N	RGD:5509061	20200514	MGI			
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0004477	turbinate hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20200514	MGI			
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18634873
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0030188	round snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:16571658
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0030258	small mandibular condyloid process		IAGP		N	RGD:5509061	20171019	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0030261	abnormal temporal bone zygomatic process morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:22194846
1315477	Prkra	protein kinase, interferon inducible double stranded RNA dependent activator	gene	MP:0030283	small mandibular coronoid process		IAGP		N	RGD:5509061	20171102	MGI			PMID:22194846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934170
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934170
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18284467
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18284467
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934170
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0004549	small trachea		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0004552	fused tracheal cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773073
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0010883	trachea stenosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:10934170
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18773073
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0012547	spina bifida cystica		IAGP		N	RGD:5509061	20141003	MGI			PMID:11943846
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0013752	stridor		IAGP		N	RGD:5509061	20150416	MGI			PMID:10934170
1315479	Traf4	TNF receptor associated factor 4	gene	MP:0031086	wheezing		IAGP		N	RGD:5509061	20200709	MGI			PMID:11943846
1315486	Atp8b4	ATPase, class I, type 8B, member 4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1315486	Atp8b4	ATPase, class I, type 8B, member 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1315486	Atp8b4	ATPase, class I, type 8B, member 4	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0001586	abnormal erythrocyte cell number		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0002309	abnormal vital capacity		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20160616	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20161027	MGI			PMID:25843683
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20161027	MGI			PMID:25843683
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0005585	increased tidal volume		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0010042	abnormal oval cell physiology		IAGP		N	RGD:5509061	20161027	MGI			PMID:25843683
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0010896	decreased lung compliance		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0010936	decreased airway resistance		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0010937	increased total lung capacity		IAGP		N	RGD:5509061	20160512	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0014275	increased respiration		IAGP		N	RGD:5509061	20230810	MGI			PMID:25712208
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0020253	increased collagen level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25843683
1315488	Adamts7	ADAM metallopeptidase with thrombospondin type 1 motif 7	gene	MP:0020316	decreased vascular endothelial cell proliferation		IAGP		N	RGD:5509061	20160616	MGI			PMID:25712208
1315492	Rev1	REV1, DNA directed polymerase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476771
1315492	Rev1	REV1, DNA directed polymerase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653636
1315492	Rev1	REV1, DNA directed polymerase	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476771
1315492	Rev1	REV1, DNA directed polymerase	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476771
1315492	Rev1	REV1, DNA directed polymerase	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587019
1315492	Rev1	REV1, DNA directed polymerase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476771
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20375278
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590289
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18400300
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12794146
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590289
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20375278
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20375278
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20201022	MGI			
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20375278
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943797
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943797
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943797
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590289
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590289
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943797
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943797
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20375278
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20375278
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0011369	increased renal glomerulus apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590289
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590289
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0014375	increased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:20375278
1315494	C1qa	complement component 1, q subcomponent, alpha polypeptide	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:20375278
1315495	Nat10	N-acetyltransferase 10	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29703891
1315495	Nat10	N-acetyltransferase 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:29703891
1315495	Nat10	N-acetyltransferase 10	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:29703891
1315495	Nat10	N-acetyltransferase 10	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20250102	MGI			PMID:36898834
1315495	Nat10	N-acetyltransferase 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220721	MGI			PMID:29703891
1315495	Nat10	N-acetyltransferase 10	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20250102	MGI			PMID:36898834
1315495	Nat10	N-acetyltransferase 10	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20220721	MGI			PMID:29703891
1315495	Nat10	N-acetyltransferase 10	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20250102	MGI			PMID:36898834
1315495	Nat10	N-acetyltransferase 10	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:29703891
1315495	Nat10	N-acetyltransferase 10	gene	MP:0020955	increased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20250102	MGI			PMID:36898834
1315497	Adgrf4	adhesion G protein-coupled receptor F4	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20220811	MGI			
1315498	Nudt7	nudix hydrolase 7	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20191128	MGI			PMID:30143643
1315498	Nudt7	nudix hydrolase 7	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20191128	MGI			PMID:30143643
1315498	Nudt7	nudix hydrolase 7	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20191128	MGI			PMID:30143643
1315498	Nudt7	nudix hydrolase 7	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20191128	MGI			PMID:30143643
1315498	Nudt7	nudix hydrolase 7	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20191128	MGI			PMID:30143643
1315498	Nudt7	nudix hydrolase 7	gene	MP:0020847	abnormal peroxisome physiology		IAGP		N	RGD:5509061	20191128	MGI			PMID:30143643
1315500	Mrps35	mitochondrial ribosomal protein S35	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1315500	Mrps35	mitochondrial ribosomal protein S35	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160804	MGI			
1315500	Mrps35	mitochondrial ribosomal protein S35	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20160804	MGI			
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955062
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0001512	trunk curl		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0004422	small temporal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0004473	absent nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0006211	small orbits		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0006284	absent hypaxial muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955062
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0013929	absent eye muscles		IAGP		N	RGD:5509061	20171026	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0013964	absent tongue muscles		IAGP		N	RGD:5509061	20171026	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0030208	abnormal intrinsic tongue muscle morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:15788460
1315509	Six4	sine oculis-related homeobox 4	gene	MP:0030210	abnormal genioglossus muscle morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:15788460
1315511	B3galt5	UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1315514	Bicdl2	BICD family like cargo adaptor 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1315514	Bicdl2	BICD family like cargo adaptor 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1315514	Bicdl2	BICD family like cargo adaptor 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1315514	Bicdl2	BICD family like cargo adaptor 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1315516	Mcmbp	minichromosome maintenance complex binding protein	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1315516	Mcmbp	minichromosome maintenance complex binding protein	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1315516	Mcmbp	minichromosome maintenance complex binding protein	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20221215	MGI			
1315516	Mcmbp	minichromosome maintenance complex binding protein	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1315516	Mcmbp	minichromosome maintenance complex binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315516	Mcmbp	minichromosome maintenance complex binding protein	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1315518	Nrap	nebulin-related anchoring protein	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1315519	Sigirr	single immunoglobulin and toll-interleukin 1 receptor (TIR) domain	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925853
1315519	Sigirr	single immunoglobulin and toll-interleukin 1 receptor (TIR) domain	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993616
1315519	Sigirr	single immunoglobulin and toll-interleukin 1 receptor (TIR) domain	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993616
1315519	Sigirr	single immunoglobulin and toll-interleukin 1 receptor (TIR) domain	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993616
1315519	Sigirr	single immunoglobulin and toll-interleukin 1 receptor (TIR) domain	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993616
1315519	Sigirr	single immunoglobulin and toll-interleukin 1 receptor (TIR) domain	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925853
1315519	Sigirr	single immunoglobulin and toll-interleukin 1 receptor (TIR) domain	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993616
1315519	Sigirr	single immunoglobulin and toll-interleukin 1 receptor (TIR) domain	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925853
1315519	Sigirr	single immunoglobulin and toll-interleukin 1 receptor (TIR) domain	gene	MP:0009334	abnormal splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925853
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0002710	increased glucagon secretion		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20160707	MGI			PMID:26086111
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0009180	increased pancreatic delta cell number		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20160707	MGI			PMID:26086111
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0014117	increased pancreatic beta cell apoptosis		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315526	Aldh1b1	aldehyde dehydrogenase 1 family, member B1	gene	MP:0014121	increased pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20161013	MGI			PMID:26518685
1315528	Tfcp2	transcription factor CP2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995745
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240307	MGI			PMID:37601242
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20240307	MGI			PMID:37601242
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20240307	MGI			PMID:37601242
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20240307	MGI			PMID:37601242
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20240307	MGI			PMID:37601242
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20240307	MGI			PMID:37601242
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:37601242
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20240307	MGI			PMID:37601242
1315530	Cabcoco1	ciliary associated calcium binding coiled-coil 1	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20240307	MGI			PMID:37601242
1315533	Clmn	calmin	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0008599	increased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:31036553
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0011164	panniculitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315536	Mta2	metastasis-associated gene family, member 2	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353770
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0000503	excessive digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0001664	abnormal digestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213841
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213841
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213841
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0006003	abnormal large intestinal transit time		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20181227	MGI			
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0011082	abnormal gastrointestinal motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315540	Gpr39	G protein-coupled receptor 39	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030183
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000416	sparse hair		IEA		N	RGD:5509061	20141003	MGI			
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0000418	focal hair loss		IEA		N	RGD:5509061	20141003	MGI			
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20141003	MGI			
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540851
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540851
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22401818
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12540851
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22401818
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675709
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0009328	delayed heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1836514
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572089
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7624372
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7830794
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260507	MGI			PMID:12552125
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:18550854
1315544	Tal1	T cell acute lymphocytic leukemia 1	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:18550854
1315551	Pigk	phosphatidylinositol glycan anchor biosynthesis, class K	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1315551	Pigk	phosphatidylinositol glycan anchor biosynthesis, class K	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20230810	MGI			PMID:33392778
1315551	Pigk	phosphatidylinositol glycan anchor biosynthesis, class K	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315551	Pigk	phosphatidylinositol glycan anchor biosynthesis, class K	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1315554	Txndc16	thioredoxin domain containing 16	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20260402	MGI			
1315556	Tbcc	tubulin-specific chaperone C	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240926	MGI			
1315556	Tbcc	tubulin-specific chaperone C	gene	MP:0004964	absent inner cell mass		IEA		N	RGD:5509061	20240926	MGI			
1315556	Tbcc	tubulin-specific chaperone C	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220519	MGI			
1315556	Tbcc	tubulin-specific chaperone C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1315556	Tbcc	tubulin-specific chaperone C	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1315556	Tbcc	tubulin-specific chaperone C	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1315558	Rnf125	ring finger protein 125	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1315560	Gtpbp1	GTP binding protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938096
1315566	Prodh2	proline dehydrogenase (oxidase) 2	gene	MP:0006272	abnormal urine organic anion level		IAGP		N	RGD:5509061	20201210	MGI			PMID:31821850
1315566	Prodh2	proline dehydrogenase (oxidase) 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20201210	MGI			PMID:31821850
1315566	Prodh2	proline dehydrogenase (oxidase) 2	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20201210	MGI			PMID:31821850
1315566	Prodh2	proline dehydrogenase (oxidase) 2	gene	MP:0011517	hyperoxaluria		IAGP		N	RGD:5509061	20201210	MGI			PMID:31821850
1315566	Prodh2	proline dehydrogenase (oxidase) 2	gene	MP:0030681	increased circulating hydroxyproline level		IAGP		N	RGD:5509061	20201210	MGI			PMID:31821850
1315566	Prodh2	proline dehydrogenase (oxidase) 2	gene	MP:0030682	hydroxyprolinuria		IAGP		N	RGD:5509061	20201210	MGI			PMID:31821850
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0008041	absent NK T cells		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20151022	MGI			PMID:26438836
1315570	Kdelr1	KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:26438836
1315578	S100a16	S100 calcium binding protein A16	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1315578	S100a16	S100 calcium binding protein A16	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1315578	S100a16	S100 calcium binding protein A16	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20201022	MGI			
1315578	S100a16	S100 calcium binding protein A16	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20221222	MGI			PMID:35914619
1315578	S100a16	S100 calcium binding protein A16	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20221222	MGI			PMID:35914619
1315578	S100a16	S100 calcium binding protein A16	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20221222	MGI			PMID:35914619
1315578	S100a16	S100 calcium binding protein A16	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20221222	MGI			PMID:35914619
1315578	S100a16	S100 calcium binding protein A16	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1315582	Ube3d	ubiquitin protein ligase E3D	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25872646
1315582	Ube3d	ubiquitin protein ligase E3D	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25872646
1315582	Ube3d	ubiquitin protein ligase E3D	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170314	MGI			PMID:25872646
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22405651
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22405651
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22405651
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22405651
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22405651
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22405651
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22405651
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0008854	bleb		IEA		N	RGD:5509061	20221215	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22405651
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22405651
1315585	Glmn	glomulin, FKBP associated protein	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20230727	MGI			PMID:37300435
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652001
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20230720	MGI			PMID:37300435
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001524	impaired limb coordination		IEA		N	RGD:5509061	20150702	MGI			
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:37300435
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0002983	increased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652001
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:37300435
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:37300435
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652001
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0005241	abnormal retina ganglion layer morphology		IEA		N	RGD:5509061	20160428	MGI			
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0005551	abnormal eye electrophysiology		IEA		N	RGD:5509061	20160428	MGI			
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:9670004
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0006095	absent amacrine cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652001
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0006095	absent amacrine cells		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652001
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008107	absent retina horizontal cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652001
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008107	absent retina horizontal cells		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008445	increased retina cone cell number		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008448	abnormal retina cone cell inner segment morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:37300435
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:37300435
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008450	retina photoreceptor degeneration		IEA		N	RGD:5509061	20160428	MGI			
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008454	absent retina rod cells		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652001
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008520	disorganized retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652001
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008520	disorganized retina outer plexiform layer		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008581	disorganized photoreceptor inner segment		IAGP		N	RGD:5509061	20230727	MGI			PMID:37300435
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008583	absent photoreceptor inner segment		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20170803	MGI			PMID:25296752
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20230727	MGI			PMID:37300435
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652001
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:40393451
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20260507	MGI			PMID:40393451
1315589	Rorb	RAR-related orphan receptor beta	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IEA		N	RGD:5509061	20240404	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20210520	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210520	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1315591	Nav1	neuron navigator 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463376
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463376
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463376
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463376
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463376
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463376
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463376
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:11463376
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11352070
1315593	Tbpl1	TATA box binding protein-like 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:11352070
1315600	Dmwd	dystrophia myotonica-containing WD repeat motif	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1315600	Dmwd	dystrophia myotonica-containing WD repeat motif	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000379	decreased hair follicle number		IEA		N	RGD:5509061	20220707	MGI			
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000384	distorted hair follicle pattern		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000472	abnormal stomach non-glandular epithelium morphology		IAGP		N	RGD:5509061	20260528	MGI			PMID:32944951
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464327
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20141003	MGI			
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20141003	MGI			
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464327
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464327
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0003164	decreased posterior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0003413	hair follicle degeneration		IEA		N	RGD:5509061	20220707	MGI			
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0003752	increased oral papilloma incidence		IAGP		N	RGD:5509061	20260528	MGI			PMID:32944951
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0003809	abnormal hair shaft morphology		IEA		N	RGD:5509061	20220714	MGI			
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0004425	abnormal otolith organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20260528	MGI			PMID:32944951
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0008861	abnormal hair shedding		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0008861	abnormal hair shedding		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0009515	increased gastrointestinal stromal tumor incidence		IAGP		N	RGD:5509061	20260528	MGI			PMID:32944951
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0009537	interstitial cells of Cajal hyperplasia		IAGP		N	RGD:5509061	20260528	MGI			PMID:32944951
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0009545	abnormal dermis papillary layer morphology		IEA		N	RGD:5509061	20220714	MGI			
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12067728
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0010678	abnormal skin adnexa morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0010686	abnormal hair follicle matrix region morphology		IEA		N	RGD:5509061	20220714	MGI			
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0010779	abnormal stomach muscularis externa morphology		IAGP		N	RGD:5509061	20260528	MGI			PMID:32944951
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0010783	abnormal stomach wall morphology		IAGP		N	RGD:5509061	20260528	MGI			PMID:32944951
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0011238	abnormal inner ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20240405	MGI			PMID:24086156
1315603	Lrig1	leucine-rich repeats and immunoglobulin-like domains 1	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:24086156
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20200514	MGI			
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20200514	MGI			
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20200514	MGI			
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0002776	increased Sertoli cell number		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20200514	MGI			
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20200514	MGI			
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0009853	decreased Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0020142	increased anti-sperm antibody level		IAGP		N	RGD:5509061	20160616	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0020355	abnormal Sertoli cell barrier morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0020356	abnormal Sertoli cell barrier function		IAGP		N	RGD:5509061	20160915	MGI			PMID:24803656
1315605	Mex3b	mex3 RNA binding family member B	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20160421	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20160811	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20160225	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20160225	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20160225	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160225	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20160225	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20160811	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20160421	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160707	MGI			PMID:25620209
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0002583	absent extraembryonic ectoderm		IAGP		N	RGD:5509061	20170629	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20170629	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20160225	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20190502	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160225	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20170629	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0011191	increased embryonic epiblast cell apoptosis		IAGP		N	RGD:5509061	20170629	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0012159	absent anterior visceral endoderm		IAGP		N	RGD:5509061	20170629	MGI			PMID:25480920
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1315611	Chd1	chromodomain helicase DNA binding protein 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1315615	Enam	enamelin	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0000122	premature tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0001664	abnormal digestion		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649948
1315615	Enam	enamelin	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649948
1315615	Enam	enamelin	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15271968
1315615	Enam	enamelin	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0002649	abnormal enamel rod pattern		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0002817	abnormal tooth mineralization		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0003053	delayed tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:15271968
1315615	Enam	enamelin	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649948
1315615	Enam	enamelin	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649948
1315615	Enam	enamelin	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0008851	decreased hemoglobin concentration distribution width		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0010096	abnormal incisor color		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0010096	abnormal incisor color		IAGP		N	RGD:5509061	20171005	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0010747	abnormal enamel organ morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0011894	decreased circulating transferrin level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0014982	decreased amylase activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:22813216
1315615	Enam	enamelin	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0030138	abnormal lower incisor color		IAGP		N	RGD:5509061	20171005	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0030139	abnormal upper incisor color		IAGP		N	RGD:5509061	20171005	MGI			PMID:15271968
1315615	Enam	enamelin	gene	MP:0030139	abnormal upper incisor color		IAGP		N	RGD:5509061	20171005	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0030220	mandibular cyst		IAGP		N	RGD:5509061	20171019	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0030221	maxillary cyst		IAGP		N	RGD:5509061	20171019	MGI			PMID:24603688
1315615	Enam	enamelin	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20180125	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0030458	abnormal tooth wear		IAGP		N	RGD:5509061	20180125	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0030459	abnormal tooth attrition		IAGP		N	RGD:5509061	20180125	MGI			PMID:18252720
1315615	Enam	enamelin	gene	MP:0030514	absent Tomes' process		IAGP		N	RGD:5509061	20180111	MGI			PMID:24603688
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20210617	MGI			PMID:33355202
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20210617	MGI			PMID:33355202
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20210617	MGI			PMID:33355202
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20210617	MGI			PMID:33355202
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20210617	MGI			PMID:33355202
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0010343	increased lipoma incidence		IAGP		N	RGD:5509061	20210617	MGI			PMID:33355202
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210617	MGI			PMID:33355202
1315619	Usp24	ubiquitin specific peptidase 24	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210617	MGI			PMID:33355202
1315620	Rad51ap1	RAD51 associated protein 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1315620	Rad51ap1	RAD51 associated protein 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1315620	Rad51ap1	RAD51 associated protein 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1315623	Naf1	nuclear assembly factor 1 ribonucleoprotein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170119	MGI			PMID:27510903
1315623	Naf1	nuclear assembly factor 1 ribonucleoprotein	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20170119	MGI			PMID:27510903
1315625	Mta3	metastasis associated 3	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1315625	Mta3	metastasis associated 3	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1315625	Mta3	metastasis associated 3	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20141003	MGI			
1315625	Mta3	metastasis associated 3	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1315625	Mta3	metastasis associated 3	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1315625	Mta3	metastasis associated 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1315625	Mta3	metastasis associated 3	gene	MP:0003062	abnormal coping response		IEA		N	RGD:5509061	20160804	MGI			
1315625	Mta3	metastasis associated 3	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1315625	Mta3	metastasis associated 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20160804	MGI			
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213585
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213585
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213585
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213585
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0004142	abnormal muscle tone		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213585
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213585
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0009436	fragmentation of sleep/wake states		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0012287	increased frequency of paradoxical sleep		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0012288	abnormal paradoxical sleep pattern		IAGP		N	RGD:5509061	20150305	MGI			PMID:22884328
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0013916	decreased intestine length		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0013958	decreased small intestine length		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0014575	increased intestinal transit time		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1315629	Mbnl2	muscleblind like splicing factor 2	gene	MP:0031756	first degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:24293317
1315631	Vpreb3	V-set pre-B cell surrogate light chain 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1315633	Lsm4	LSM4 homolog, U6 small nuclear RNA and mRNA degradation associated	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10629062
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20181227	MGI			
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20181227	MGI			
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20180301	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0030718	increased circulating lysine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:28923496
1315634	Nadk2	NAD kinase 2, mitochondrial	gene	MP:0030721	increased lysine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:28923496
1315637	Hepacam	hepatocyte cell adhesion molecule	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28695146
1315637	Hepacam	hepatocyte cell adhesion molecule	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24647135
1315637	Hepacam	hepatocyte cell adhesion molecule	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24647135
1315637	Hepacam	hepatocyte cell adhesion molecule	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20190425	MGI			PMID:28695146
1315637	Hepacam	hepatocyte cell adhesion molecule	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20150827	MGI			PMID:24647135
1315637	Hepacam	hepatocyte cell adhesion molecule	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20190425	MGI			PMID:28695146
1315637	Hepacam	hepatocyte cell adhesion molecule	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24647135
1315637	Hepacam	hepatocyte cell adhesion molecule	gene	MP:0011854	cerebral edema		IAGP		N	RGD:5509061	20190425	MGI			PMID:28695146
1315640	Acsm1	acyl-CoA synthetase medium-chain family member 1	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20230601	MGI			
1315640	Acsm1	acyl-CoA synthetase medium-chain family member 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1315640	Acsm1	acyl-CoA synthetase medium-chain family member 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1315640	Acsm1	acyl-CoA synthetase medium-chain family member 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1315644	Kif3b	kinesin family member 3B	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20220421	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1315644	Kif3b	kinesin family member 3B	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1315644	Kif3b	kinesin family member 3B	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1315644	Kif3b	kinesin family member 3B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865700
1315644	Kif3b	kinesin family member 3B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315644	Kif3b	kinesin family member 3B	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0012445	thin hippocampus stratum radiatum		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0012775	abnormal brain weight		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1315644	Kif3b	kinesin family member 3B	gene	MP:0020512	abnormal dendritic mushroom spine morphology		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315644	Kif3b	kinesin family member 3B	gene	MP:0020870	decreased thigmotaxis		IAGP		N	RGD:5509061	20200528	MGI			PMID:31746486
1315646	Fermt1	fermitin family member 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0009485	distended ileum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0009511	distended stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0030578	decreased keratinocyte adhesion		IAGP		N	RGD:5509061	20180607	MGI			PMID:19057668
1315646	Fermt1	fermitin family member 1	gene	MP:0030584	skin atrophy		IAGP		N	RGD:5509061	20180614	MGI			PMID:19057668
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18218778
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18218778
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18218778
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20180809	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20180809	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20180809	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18218778
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20190221	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18218778
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0003335	exocrine pancreatic insufficiency		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0004248	abnormal epaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18218778
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18218778
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20190221	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20180809	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20180809	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20180809	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18218778
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150521	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180809	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:18218778
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20161013	MGI			PMID:25574476
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0020309	increased creatine kinase activity		IAGP		N	RGD:5509061	20180809	MGI			PMID:28175314
1315650	Ptrh2	peptidyl-tRNA hydrolase 2	gene	MP:0030798	joint contracture		IAGP		N	RGD:5509061	20190221	MGI			PMID:28175314
1315651	Edrf1	erythroid differentiation regulatory factor 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1315651	Edrf1	erythroid differentiation regulatory factor 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1315651	Edrf1	erythroid differentiation regulatory factor 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20231214	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20231214	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0012431	increased lymphoma incidence		IEA		N	RGD:5509061	20141003	MGI			
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0020850	abnormal microtubule cytoskeleton morphology		IAGP		N	RGD:5509061	20231214	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20231214	MGI			PMID:20861308
1315653	Myh14	myosin, heavy polypeptide 14	gene	MP:0031611	decreased fetal cardiomyocyte number		IAGP		N	RGD:5509061	20240321	MGI			PMID:20861308
1315655	Carf	calcium response factor	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519520
1315655	Carf	calcium response factor	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20220519	MGI			
1315655	Carf	calcium response factor	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1315655	Carf	calcium response factor	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519520
1315655	Carf	calcium response factor	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519520
1315655	Carf	calcium response factor	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20210128	MGI			
1315655	Carf	calcium response factor	gene	MP:0014365	impaired short-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:20519520
1315657	Donson	downstream neighbor of SON	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20240104	MGI			PMID:37590370
1315657	Donson	downstream neighbor of SON	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20240104	MGI			PMID:37590370
1315657	Donson	downstream neighbor of SON	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240104	MGI			PMID:37590370
1315657	Donson	downstream neighbor of SON	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20240104	MGI			PMID:37590370
1315657	Donson	downstream neighbor of SON	gene	MP:0009850	embryonic lethality between implantation and placentation		IAGP		N	RGD:5509061	20180524	MGI			PMID:28630177
1315665	C1qc	complement component 1, q subcomponent, C chain	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1315665	C1qc	complement component 1, q subcomponent, C chain	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20210826	MGI			
1315665	C1qc	complement component 1, q subcomponent, C chain	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20241121	MGI			
1315665	C1qc	complement component 1, q subcomponent, C chain	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20210826	MGI			
1315665	C1qc	complement component 1, q subcomponent, C chain	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1315665	C1qc	complement component 1, q subcomponent, C chain	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1315665	C1qc	complement component 1, q subcomponent, C chain	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1315665	C1qc	complement component 1, q subcomponent, C chain	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1315667	Gpr33	G protein-coupled receptor 33	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160421	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210520	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559454
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20220519	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559454
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20240509	MGI			PMID:34359900
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20201022	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20201022	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20240509	MGI			PMID:34359900
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210128	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559454
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004233	abnormal muscle weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843959
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559454
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21941299
1315669	Stim1	stromal interaction molecule 1	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559454
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008407	decreased cellular sensitivity to hydrogen peroxide		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746875
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009425	increased soleus weight		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009425	increased soleus weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559454
1315669	Stim1	stromal interaction molecule 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0010089	abnormal circulating creatine kinase level		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20240509	MGI			PMID:34359900
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559454
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059272
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18327260
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011585	decreased alkaline phosphatase activity		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20240509	MGI			PMID:34359900
1315669	Stim1	stromal interaction molecule 1	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17965774
1315669	Stim1	stromal interaction molecule 1	gene	MP:0013022	increased Ly6C high monocyte number		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0013026	decreased Ly6C low monocyte number		IAGP		N	RGD:5509061	20230420	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0013621	decreased internal diameter of femur		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0013639	decreased bone stiffness		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0014292	decreased internal diameter of tibia		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:21530328
1315669	Stim1	stromal interaction molecule 1	gene	MP:0014652	increased skeletal muscle fiber mitochondrial size		IAGP		N	RGD:5509061	20250410	MGI			PMID:30576443
1315669	Stim1	stromal interaction molecule 1	gene	MP:0014914	increased muscle cell calcium uptake		IAGP		N	RGD:5509061	20260219	MGI			PMID:31666234
1315669	Stim1	stromal interaction molecule 1	gene	MP:0020240	increased skeletal muscle cell apoptosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:34359900
1315669	Stim1	stromal interaction molecule 1	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20240509	MGI			PMID:34359900
1315669	Stim1	stromal interaction molecule 1	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20240509	MGI			PMID:34359900
1315669	Stim1	stromal interaction molecule 1	gene	MP:0031402	decreased muscle fatigability		IAGP		N	RGD:5509061	20240509	MGI			PMID:30576443
1315673	Prima1	proline rich membrane anchor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357277
1315673	Prima1	proline rich membrane anchor 1	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357277
1315673	Prima1	proline rich membrane anchor 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357277
1315675	Mcm3ap	minichromosome maintenance complex component 3 associated protein	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1315675	Mcm3ap	minichromosome maintenance complex component 3 associated protein	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1315675	Mcm3ap	minichromosome maintenance complex component 3 associated protein	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1315675	Mcm3ap	minichromosome maintenance complex component 3 associated protein	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1315675	Mcm3ap	minichromosome maintenance complex component 3 associated protein	gene	MP:0008093	abnormal memory B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1315675	Mcm3ap	minichromosome maintenance complex component 3 associated protein	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1315675	Mcm3ap	minichromosome maintenance complex component 3 associated protein	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1315675	Mcm3ap	minichromosome maintenance complex component 3 associated protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17903179
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20181227	MGI			
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20150129	MGI			PMID:21052544
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849587
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210520	MGI			
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220811	MGI			
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849587
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849587
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0008025	brain vacuoles		IEA		N	RGD:5509061	20141003	MGI			
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849587
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849587
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849587
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849587
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849587
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849587
1315677	Pde6a	phosphodiesterase 6A, cGMP-specific, rod, alpha	gene	MP:0012671	retina spots		IEA		N	RGD:5509061	20141003	MGI			
1315682	Plgrkt	plasminogen receptor, C-terminal lysine transmembrane protein	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200123	MGI			PMID:27714956
1315682	Plgrkt	plasminogen receptor, C-terminal lysine transmembrane protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200123	MGI			PMID:27714956
1315682	Plgrkt	plasminogen receptor, C-terminal lysine transmembrane protein	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27714956
1315682	Plgrkt	plasminogen receptor, C-terminal lysine transmembrane protein	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20200123	MGI			PMID:27714956
1315682	Plgrkt	plasminogen receptor, C-terminal lysine transmembrane protein	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20200123	MGI			PMID:27714956
1315682	Plgrkt	plasminogen receptor, C-terminal lysine transmembrane protein	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20200123	MGI			PMID:27714956
1315682	Plgrkt	plasminogen receptor, C-terminal lysine transmembrane protein	gene	MP:0020212	impaired leukocyte migration		IAGP		N	RGD:5509061	20200123	MGI			PMID:27714956
1315685	Ints11	integrator complex subunit 11	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:40780182
1315685	Ints11	integrator complex subunit 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315687	Ca7	carbonic anhydrase 7	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23881097
1315687	Ca7	carbonic anhydrase 7	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:23881097
1315690	Retreg2	reticulophagy regulator family member 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1315690	Retreg2	reticulophagy regulator family member 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20200514	MGI			
1315690	Retreg2	reticulophagy regulator family member 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20200514	MGI			
1315690	Retreg2	reticulophagy regulator family member 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20200514	MGI			
1315690	Retreg2	reticulophagy regulator family member 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1315690	Retreg2	reticulophagy regulator family member 2	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1315690	Retreg2	reticulophagy regulator family member 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1315692	Il18rap	interleukin 18 receptor accessory protein	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1315692	Il18rap	interleukin 18 receptor accessory protein	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1315692	Il18rap	interleukin 18 receptor accessory protein	gene	MP:0002073	abnormal hair growth		IEA		N	RGD:5509061	20201022	MGI			
1315692	Il18rap	interleukin 18 receptor accessory protein	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843532
1315692	Il18rap	interleukin 18 receptor accessory protein	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843532
1315692	Il18rap	interleukin 18 receptor accessory protein	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1315692	Il18rap	interleukin 18 receptor accessory protein	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20210826	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:15009730
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20231207	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0001324	abnormal eye pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20231207	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109702
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20231207	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20231207	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0002894	abnormal otolith morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109702
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0002963	decreased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:5367369
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0002980	abnormal postural reflex		IEA		N	RGD:5509061	20111116	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0003173	decreased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0004721	abnormal platelet dense granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0004812	abnormal linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109702
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15009730
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:11912185
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005102	abnormal iris pigmentation		IEA		N	RGD:5509061	20231207	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20160811	MGI			PMID:11912185
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005191	head tilt		IEA		N	RGD:5509061	20111116	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20160811	MGI			PMID:11912185
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20260402	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1912584
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20231207	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20231207	MGI			
1315694	Bloc1s5	biogenesis of lysosomal organelles complex-1, subunit 5, muted	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:1912584
1315698	H4c1	H4 clustered histone 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1315698	H4c1	H4 clustered histone 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1315698	H4c1	H4 clustered histone 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1315698	H4c1	H4 clustered histone 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20250508	MGI			
1315698	H4c1	H4 clustered histone 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1315700	Xrcc3	X-ray repair complementing 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20220721	MGI			PMID:34601382
1315700	Xrcc3	X-ray repair complementing 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20220721	MGI			PMID:34601382
1315700	Xrcc3	X-ray repair complementing 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20220721	MGI			PMID:34601382
1315700	Xrcc3	X-ray repair complementing 3	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1315700	Xrcc3	X-ray repair complementing 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:34601382
1315700	Xrcc3	X-ray repair complementing 3	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:34601382
1315700	Xrcc3	X-ray repair complementing 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:34601382
1315700	Xrcc3	X-ray repair complementing 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000577	absent eccrine glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000819	abnormal olfactory bulb morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0002199	abnormal brain commissure morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0002219	decreased lymph node number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0002717	abnormal male preputial gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003253	dilated bile duct		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003262	intestinal/bowel diverticulum		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003584	bifid ureter		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0003931	absent molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0004056	abnormal myocardium compact layer morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0004666	absent stapedial artery		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0005004	abnormal lymphocyte anergy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0005046	absent spleen white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0005107	abnormal stapes morphology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18423196
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008387	hypochromic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18423196
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097000
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0010572	persistent right dorsal aorta		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0010912	herniated liver		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10215628
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421844
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0012303	umbilical vein stenosis		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013382	small perianal sebaceous gland		IAGP		N	RGD:5509061	20141218	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013385	abnormal Meibomian gland development		IAGP		N	RGD:5509061	20141225	MGI			PMID:12060722
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013842	ductus venosus stenosis		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013878	abnormal ductus venosus valve topology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013917	persistent right 6th pharyngeal arch artery		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013918	abnormal endolymphatic sac topology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013975	abnormal coronary sinus connection		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1315707	Traf6	TNF receptor-associated factor 6	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1315709	Mlf1	myeloid leukemia factor 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:26563351
1315709	Mlf1	myeloid leukemia factor 1	gene	MP:0009341	decreased splenocyte apoptosis		IAGP		N	RGD:5509061	20190103	MGI			PMID:26563351
1315709	Mlf1	myeloid leukemia factor 1	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20190103	MGI			PMID:26563351
1315713	Cdh7	cadherin 7, type 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1315718	Kin	Kin17 DNA and RNA binding protein	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20241121	MGI			
1315718	Kin	Kin17 DNA and RNA binding protein	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1315718	Kin	Kin17 DNA and RNA binding protein	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20220811	MGI			
1315718	Kin	Kin17 DNA and RNA binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1315718	Kin	Kin17 DNA and RNA binding protein	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1315721	Ralgapb	Ral GTPase activating protein, beta subunit (non-catalytic)	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1315721	Ralgapb	Ral GTPase activating protein, beta subunit (non-catalytic)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315724	Cd34	CD34 antigen	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483328
1315724	Cd34	CD34 antigen	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483328
1315724	Cd34	CD34 antigen	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483328
1315724	Cd34	CD34 antigen	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483328
1315724	Cd34	CD34 antigen	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483328
1315724	Cd34	CD34 antigen	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8555469
1315724	Cd34	CD34 antigen	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483328
1315724	Cd34	CD34 antigen	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8611677
1315724	Cd34	CD34 antigen	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8555469
1315724	Cd34	CD34 antigen	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483328
1315724	Cd34	CD34 antigen	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8555469
1315724	Cd34	CD34 antigen	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8555469
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636176
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636176
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636176
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0009688	abnormal spinal cord central canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0009689	abnormal neural tube ventricular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720556
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0009827	skin detachment		IAGP		N	RGD:5509061	20170309	MGI			PMID:9250866
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0009964	abnormal cerebellum lobule morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636176
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0012526	abnormal upper rhombic lip morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636176
1315729	Rab23	RAB23, member RAS oncogene family	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1315731	Brpf3	bromodomain and PHD finger containing, 3	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1315731	Brpf3	bromodomain and PHD finger containing, 3	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20160804	MGI			
1315733	Il36a	interleukin 36A	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20201210	MGI			PMID:29794016
1315733	Il36a	interleukin 36A	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20201210	MGI			PMID:29794016
1315736	Rhobtb1	Rho-related BTB domain containing 1	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20200514	MGI			
1315736	Rhobtb1	Rho-related BTB domain containing 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20250508	MGI			
1315736	Rhobtb1	Rho-related BTB domain containing 1	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20200514	MGI			
1315736	Rhobtb1	Rho-related BTB domain containing 1	gene	MP:0008127	decreased dendritic cell number		IEA		N	RGD:5509061	20260402	MGI			
1315736	Rhobtb1	Rho-related BTB domain containing 1	gene	MP:0013679	increased Ly6C-positive NK T cell number		IEA		N	RGD:5509061	20210826	MGI			
1315738	Dock5	dedicator of cytokinesis 5	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:9093026
1315738	Dock5	dedicator of cytokinesis 5	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315738	Dock5	dedicator of cytokinesis 5	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315738	Dock5	dedicator of cytokinesis 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820033
1315739	Tecpr1	tectonin beta-propeller repeat containing 1	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21575909
1315739	Tecpr1	tectonin beta-propeller repeat containing 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21575909
1315748	Vps26c	VPS26 endosomal protein sorting factor C	gene	MP:0000603	pale liver		IEA		N	RGD:5509061	20210826	MGI			
1315748	Vps26c	VPS26 endosomal protein sorting factor C	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20220519	MGI			
1315748	Vps26c	VPS26 endosomal protein sorting factor C	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1315748	Vps26c	VPS26 endosomal protein sorting factor C	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201022	MGI			
1315748	Vps26c	VPS26 endosomal protein sorting factor C	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20220519	MGI			
1315748	Vps26c	VPS26 endosomal protein sorting factor C	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20220519	MGI			
1315748	Vps26c	VPS26 endosomal protein sorting factor C	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20210826	MGI			
1315748	Vps26c	VPS26 endosomal protein sorting factor C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315748	Vps26c	VPS26 endosomal protein sorting factor C	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20250508	MGI			
1315749	Rimkla	ribosomal modification protein rimK-like family member A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20230223	MGI			PMID:33638175
1315749	Rimkla	ribosomal modification protein rimK-like family member A	gene	MP:0014365	impaired short-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:33638175
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20201022	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20201022	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210826	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20200514	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200514	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20231207	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20200514	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20200514	MGI			
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20220407	MGI			PMID:12950107
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220407	MGI			PMID:10471512
1315752	Csnk2a2	casein kinase 2, alpha prime polypeptide	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1315753	Frrs1	ferric-chelate reductase 1	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20211021	MGI			
1315753	Frrs1	ferric-chelate reductase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315753	Frrs1	ferric-chelate reductase 1	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20211021	MGI			
1315753	Frrs1	ferric-chelate reductase 1	gene	MP:0011941	increased fluid intake		IEA		N	RGD:5509061	20260402	MGI			
1315754	Grap	GRB2-related adaptor protein	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971956
1315754	Grap	GRB2-related adaptor protein	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971956
1315755	Fcrl2	Fc receptor like 2	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20170406	MGI			
1315755	Fcrl2	Fc receptor like 2	gene	MP:0001264	increased body size		IEA		N	RGD:5509061	20170406	MGI			
1315755	Fcrl2	Fc receptor like 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20230601	MGI			
1315755	Fcrl2	Fc receptor like 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20170406	MGI			
1315755	Fcrl2	Fc receptor like 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1315755	Fcrl2	Fc receptor like 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20170406	MGI			
1315755	Fcrl2	Fc receptor like 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20170406	MGI			
1315755	Fcrl2	Fc receptor like 2	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20230601	MGI			
1315755	Fcrl2	Fc receptor like 2	gene	MP:0012323	increased total tissue mass		IEA		N	RGD:5509061	20170406	MGI			
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135277
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135277
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0003326	liver failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135277
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0004264	abnormal extraembryonic tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135277
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135277
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135277
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135277
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135277
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0011897	decreased circulating unsaturated transferrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20210211	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0012356	increased prothrombin time		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:21907140
1315758	Fbxl5	F-box and leucine-rich repeat protein 5	gene	MP:0020369	increased intestine iron level		IAGP		N	RGD:5509061	20161020	MGI			PMID:23135277
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20241121	MGI			
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20241121	MGI			
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20241121	MGI			
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11113182
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20241121	MGI			
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9716588
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9558405
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11113182
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060151
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9716588
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20241121	MGI			
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9558405
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9716588
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0003714	absent platelets		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20241121	MGI			
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15005853
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15005853
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0009439	increased myeloid sarcoma incidence		IAGP		N	RGD:5509061	20200813	MGI			PMID:30755419
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11113182
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15005853
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0010961	increased compact bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15005853
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:15005853
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0020399	enhanced megakaryocyte emperipolesis		IAGP		N	RGD:5509061	20170803	MGI			PMID:7774011
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0020838	increased acute myeloid leukemia incidence		IAGP		N	RGD:5509061	20200813	MGI			PMID:30755419
1315760	Nfe2	nuclear factor, erythroid derived 2	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11113182
1315764	Prox1	prospero homeobox 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888866
1315764	Prox1	prospero homeobox 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888866
1315764	Prox1	prospero homeobox 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791897
1315764	Prox1	prospero homeobox 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692551
1315764	Prox1	prospero homeobox 1	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080188
1315764	Prox1	prospero homeobox 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692551
1315764	Prox1	prospero homeobox 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10499794
1315764	Prox1	prospero homeobox 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360386
1315764	Prox1	prospero homeobox 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360386
1315764	Prox1	prospero homeobox 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908929
1315764	Prox1	prospero homeobox 1	gene	MP:0002450	abnormal lymph organ development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10499794
1315764	Prox1	prospero homeobox 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10499794
1315764	Prox1	prospero homeobox 1	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0003660	chylothorax		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888866
1315764	Prox1	prospero homeobox 1	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122728
1315764	Prox1	prospero homeobox 1	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080188
1315764	Prox1	prospero homeobox 1	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0008107	absent retina horizontal cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692551
1315764	Prox1	prospero homeobox 1	gene	MP:0008269	abnormal hippocampus CA4 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791897
1315764	Prox1	prospero homeobox 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360386
1315764	Prox1	prospero homeobox 1	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0009159	increased pancreatic acinar cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122728
1315764	Prox1	prospero homeobox 1	gene	MP:0009165	abnormal endocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122728
1315764	Prox1	prospero homeobox 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0009938	abnormal hippocampus granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791897
1315764	Prox1	prospero homeobox 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0010194	absent lymphatic vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908929
1315764	Prox1	prospero homeobox 1	gene	MP:0010198	decreased lymphatic vessel endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360386
1315764	Prox1	prospero homeobox 1	gene	MP:0010416	interventricular septum membranous part aneurysm		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0010498	abnormal interventricular septum muscular part morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0010626	thick tricuspid valve cusps		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080188
1315764	Prox1	prospero homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080188
1315764	Prox1	prospero homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170315
1315764	Prox1	prospero homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10080188
1315764	Prox1	prospero homeobox 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10499794
1315764	Prox1	prospero homeobox 1	gene	MP:0011964	increased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692551
1315764	Prox1	prospero homeobox 1	gene	MP:0014731	disorganized myocardial fiber myofibrils		IAGP		N	RGD:5509061	20250911	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1315764	Prox1	prospero homeobox 1	gene	MP:0031147	abnormal ventricular thrombosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:24938781
1315766	Rbm4	RNA binding motif protein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129807
1315766	Rbm4	RNA binding motif protein 4	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129807
1315766	Rbm4	RNA binding motif protein 4	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129807
1315766	Rbm4	RNA binding motif protein 4	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129807
1315766	Rbm4	RNA binding motif protein 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129807
1315766	Rbm4	RNA binding motif protein 4	gene	MP:0008497	decreased IgG2b level		IEA		N	RGD:5509061	20160804	MGI			
1315766	Rbm4	RNA binding motif protein 4	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129807
1315766	Rbm4	RNA binding motif protein 4	gene	MP:0010147	abnormal endocrine pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129807
1315768	Zfp580	zinc finger protein 580	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1315768	Zfp580	zinc finger protein 580	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1315768	Zfp580	zinc finger protein 580	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1315769	Spns3	SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20190502	MGI			
1315769	Spns3	SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20190502	MGI			
1315769	Spns3	SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20190502	MGI			
1315769	Spns3	SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1315769	Spns3	SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1315769	Spns3	SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20190502	MGI			
1315772	Fmnl2	formin-like 2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210520	MGI			
1315772	Fmnl2	formin-like 2	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20211021	MGI			
1315772	Fmnl2	formin-like 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1315773	Igtp	interferon gamma induced GTPase	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639151
1315773	Igtp	interferon gamma induced GTPase	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908352
1315773	Igtp	interferon gamma induced GTPase	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20211118	MGI			PMID:34078740
1315773	Igtp	interferon gamma induced GTPase	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639151
1315773	Igtp	interferon gamma induced GTPase	gene	MP:0008647	increased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639151
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20190502	MGI			
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20190502	MGI			
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20190502	MGI			
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20190502	MGI			
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20190502	MGI			
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20201022	MGI			
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20190502	MGI			
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20190502	MGI			
1315775	Edc3	enhancer of mRNA decapping 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20190502	MGI			
1315778	Atp6v0d2	ATPase, H+ transporting, lysosomal V0 subunit D2	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17128270
1315778	Atp6v0d2	ATPase, H+ transporting, lysosomal V0 subunit D2	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17128270
1315778	Atp6v0d2	ATPase, H+ transporting, lysosomal V0 subunit D2	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17128270
1315778	Atp6v0d2	ATPase, H+ transporting, lysosomal V0 subunit D2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17128270
1315778	Atp6v0d2	ATPase, H+ transporting, lysosomal V0 subunit D2	gene	MP:0031073	decreased circulating type I collagen C-terminal telopeptide level		IAGP		N	RGD:5509061	20200618	MGI			PMID:17128270
1315781	Psmd7	proteasome (prosome, macropain) 26S subunit, non-ATPase, 7	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2824282
1315793	Fitm1	fat storage-inducing transmembrane protein 1	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20210429	MGI			PMID:30923760
1315793	Fitm1	fat storage-inducing transmembrane protein 1	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210429	MGI			PMID:30923760
1315795	Kyat1	kynurenine aminotransferase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1315795	Kyat1	kynurenine aminotransferase 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1315795	Kyat1	kynurenine aminotransferase 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1315795	Kyat1	kynurenine aminotransferase 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1315795	Kyat1	kynurenine aminotransferase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315795	Kyat1	kynurenine aminotransferase 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1315795	Kyat1	kynurenine aminotransferase 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1315797	Pex19	peroxisomal biogenesis factor 19	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1315797	Pex19	peroxisomal biogenesis factor 19	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1315797	Pex19	peroxisomal biogenesis factor 19	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1315797	Pex19	peroxisomal biogenesis factor 19	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1315797	Pex19	peroxisomal biogenesis factor 19	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20250508	MGI			
1315797	Pex19	peroxisomal biogenesis factor 19	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20250508	MGI			
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0000679	increased percent water in carcass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0003441	increased glycerol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20160414	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0010358	abnormal free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21969596
1315799	Lgals12	lectin, galactose binding, soluble 12	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:21969596
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158803
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158803
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158803
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158803
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1315802	Lmtk2	lemur tyrosine kinase 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158803
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20231207	MGI			
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573887
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033381
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213215
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151112	MGI			PMID:24891386
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0008799	oblique facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:16990542
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0008886	abnormal PML bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:19033381
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16990542
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16990542
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16990542
1315808	Sumo1	small ubiquitin-like modifier 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315810	Jade1	jade family PHD finger 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1315810	Jade1	jade family PHD finger 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1315810	Jade1	jade family PHD finger 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14612400
1315813	Aebp1	AE binding protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20231207	MGI			
1315813	Aebp1	AE binding protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20221103	MGI			
1315813	Aebp1	AE binding protein 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315813	Aebp1	AE binding protein 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438679
1315813	Aebp1	AE binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315813	Aebp1	AE binding protein 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299101
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20240523	MGI			
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20240523	MGI			
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191128	MGI			
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1315816	Tubgcp4	tubulin, gamma complex component 4	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20220901	MGI			PMID:31209365
1315817	Trappc2b	trafficking protein particle complex 2B	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20230720	MGI			
1315817	Trappc2b	trafficking protein particle complex 2B	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1315817	Trappc2b	trafficking protein particle complex 2B	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20230720	MGI			
1315822	Dusp18	dual specificity phosphatase 18	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1315822	Dusp18	dual specificity phosphatase 18	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1315822	Dusp18	dual specificity phosphatase 18	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1315822	Dusp18	dual specificity phosphatase 18	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20240523	MGI			
1315822	Dusp18	dual specificity phosphatase 18	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1315822	Dusp18	dual specificity phosphatase 18	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20241121	MGI			
1315824	Dynlrb2	dynein light chain roadblock-type 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1315824	Dynlrb2	dynein light chain roadblock-type 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1315824	Dynlrb2	dynein light chain roadblock-type 2	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1315824	Dynlrb2	dynein light chain roadblock-type 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20160114	MGI			
1315824	Dynlrb2	dynein light chain roadblock-type 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20170105	MGI			
1315824	Dynlrb2	dynein light chain roadblock-type 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1315824	Dynlrb2	dynein light chain roadblock-type 2	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20160114	MGI			
1315824	Dynlrb2	dynein light chain roadblock-type 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315824	Dynlrb2	dynein light chain roadblock-type 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0010637	sinus bradycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12095919
1315826	Slc30a5	solute carrier family 30 (zinc transporter), member 5	gene	MP:0031762	third degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:12095919
1315827	Mblac1	metallo-beta-lactamase domain containing 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20260122	MGI			PMID:29868674
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0000650	mesocardia		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220519	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0000694	spleen hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20220519	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0001943	abnormal respiration		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20241121	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0004880	lung cyst		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0005330	cardiomyopathy		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0010808	right-sided stomach		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0011250	abdominal situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0011649	immotile respiratory cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0011666	double outlet right ventricle, ventricular defect committed to aorta		IEA		N	RGD:5509061	20141003	MGI			
1315829	Odad2	outer dynein arm docking complex subunit 2	gene	MP:0011683	dual inferior vena cava		IAGP		N	RGD:5509061	20141003	MGI			PMID:23849778
1315831	Bcl9	B cell CLL/lymphoma 9	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19699733
1315831	Bcl9	B cell CLL/lymphoma 9	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20231207	MGI			
1315831	Bcl9	B cell CLL/lymphoma 9	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1315831	Bcl9	B cell CLL/lymphoma 9	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20231207	MGI			
1315831	Bcl9	B cell CLL/lymphoma 9	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19699733
1315831	Bcl9	B cell CLL/lymphoma 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1315831	Bcl9	B cell CLL/lymphoma 9	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1315831	Bcl9	B cell CLL/lymphoma 9	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:19699733
1315837	Cpxm1	carboxypeptidase X, M14 family member 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1315837	Cpxm1	carboxypeptidase X, M14 family member 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1315837	Cpxm1	carboxypeptidase X, M14 family member 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20220519	MGI			
1315837	Cpxm1	carboxypeptidase X, M14 family member 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750041
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750041
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750041
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17072340
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750041
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750041
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750041
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11207276
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750041
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:9109487
1315841	Mybl1	Myb proto-oncogene like 1	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:21750041
1315847	Rad51d	RAD51 paralog D	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315847	Rad51d	RAD51 paralog D	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315847	Rad51d	RAD51 paralog D	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315847	Rad51d	RAD51 paralog D	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315847	Rad51d	RAD51 paralog D	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315847	Rad51d	RAD51 paralog D	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315847	Rad51d	RAD51 paralog D	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315847	Rad51d	RAD51 paralog D	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315847	Rad51d	RAD51 paralog D	gene	MP:0008405	decreased cellular sensitivity to methylmethanesulfonate induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315847	Rad51d	RAD51 paralog D	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10705376
1315854	Insm2	insulinoma-associated 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20230406	MGI			PMID:30359270
1315854	Insm2	insulinoma-associated 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20230406	MGI			PMID:30359270
1315854	Insm2	insulinoma-associated 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20230406	MGI			PMID:30359270
1315854	Insm2	insulinoma-associated 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20230406	MGI			PMID:30359270
1315854	Insm2	insulinoma-associated 2	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20230406	MGI			PMID:30359270
1315854	Insm2	insulinoma-associated 2	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20230406	MGI			PMID:30359270
1315864	Gkap1	G kinase anchoring protein 1	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20201119	MGI			PMID:31318116
1315864	Gkap1	G kinase anchoring protein 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
1315864	Gkap1	G kinase anchoring protein 1	gene	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20201119	MGI			PMID:31318116
1315864	Gkap1	G kinase anchoring protein 1	gene	MP:0004928	increased epididymis weight		IAGP		N	RGD:5509061	20201119	MGI			PMID:31318116
1315864	Gkap1	G kinase anchoring protein 1	gene	MP:0004931	enlarged epididymis		IAGP		N	RGD:5509061	20201119	MGI			PMID:31318116
1315864	Gkap1	G kinase anchoring protein 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20201119	MGI			PMID:31318116
1315864	Gkap1	G kinase anchoring protein 1	gene	MP:0009256	enlarged corpus epididymis		IAGP		N	RGD:5509061	20201119	MGI			PMID:31318116
1315864	Gkap1	G kinase anchoring protein 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1315864	Gkap1	G kinase anchoring protein 1	gene	MP:0030603	increased sperm number		IAGP		N	RGD:5509061	20201119	MGI			PMID:31318116
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0000398	splitting of guard hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0000405	abnormal auchene hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001123	dilated uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001136	dilated uterine cervix		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001143	constricted vagina orifice		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201231	MGI			
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20160421	MGI			
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17049212
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17049212
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808631
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17049212
1315866	Ovol1	ovo like zinc finger 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17049212
1315870	Ppp2r3a	protein phosphatase 2, regulatory subunit B'', alpha	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1315870	Ppp2r3a	protein phosphatase 2, regulatory subunit B'', alpha	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736746
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22020280
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23706823
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22020280
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736746
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23706823
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736746
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22020280
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23706823
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23706823
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23706823
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736746
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22020280
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22020280
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23706823
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22020280
1315878	Piwil2	piwi-like RNA-mediated gene silencing 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:14736746
1315880	Cln5	ceroid-lipofuscinosis, neuronal 5	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459177
1315880	Cln5	ceroid-lipofuscinosis, neuronal 5	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459177
1315880	Cln5	ceroid-lipofuscinosis, neuronal 5	gene	MP:0003246	loss of GABAergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459177
1315885	Suv39h2	suppressor of variegation 3-9 2	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1315885	Suv39h2	suppressor of variegation 3-9 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1315885	Suv39h2	suppressor of variegation 3-9 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1315885	Suv39h2	suppressor of variegation 3-9 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1315885	Suv39h2	suppressor of variegation 3-9 2	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1315885	Suv39h2	suppressor of variegation 3-9 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1315885	Suv39h2	suppressor of variegation 3-9 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1315892	Rtp4	receptor transporter protein 4	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20250508	MGI			
1315892	Rtp4	receptor transporter protein 4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20231207	MGI			
1315892	Rtp4	receptor transporter protein 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1315892	Rtp4	receptor transporter protein 4	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20201112	MGI			PMID:32709745
1315892	Rtp4	receptor transporter protein 4	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1315892	Rtp4	receptor transporter protein 4	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20201112	MGI			PMID:32709745
1315892	Rtp4	receptor transporter protein 4	gene	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20201112	MGI			PMID:32709745
1315892	Rtp4	receptor transporter protein 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1315894	Btbd9	BTB domain containing 9	gene	MP:0000860	abnormal primary somatosensory cortex morphology		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1315894	Btbd9	BTB domain containing 9	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20210107	MGI			PMID:32446853
1315894	Btbd9	BTB domain containing 9	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1315894	Btbd9	BTB domain containing 9	gene	MP:0001396	unidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22678064
1315894	Btbd9	BTB domain containing 9	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1315894	Btbd9	BTB domain containing 9	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1315894	Btbd9	BTB domain containing 9	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22678064
1315894	Btbd9	BTB domain containing 9	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1315894	Btbd9	BTB domain containing 9	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1315894	Btbd9	BTB domain containing 9	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20210107	MGI			PMID:32446853
1315894	Btbd9	BTB domain containing 9	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20260402	MGI			
1315894	Btbd9	BTB domain containing 9	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1315894	Btbd9	BTB domain containing 9	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22536397
1315894	Btbd9	BTB domain containing 9	gene	MP:0003663	abnormal thermosensation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22678064
1315894	Btbd9	BTB domain containing 9	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22536397
1315894	Btbd9	BTB domain containing 9	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22536397
1315894	Btbd9	BTB domain containing 9	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1315894	Btbd9	BTB domain containing 9	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1315894	Btbd9	BTB domain containing 9	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:22678064
1315894	Btbd9	BTB domain containing 9	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22678064
1315894	Btbd9	BTB domain containing 9	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22536397
1315894	Btbd9	BTB domain containing 9	gene	MP:0009455	enhanced cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22536397
1315894	Btbd9	BTB domain containing 9	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1315894	Btbd9	BTB domain containing 9	gene	MP:0011396	abnormal sleep behavior		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1315894	Btbd9	BTB domain containing 9	gene	MP:0011396	abnormal sleep behavior		IAGP		N	RGD:5509061	20210107	MGI			PMID:32446853
1315894	Btbd9	BTB domain containing 9	gene	MP:0012448	abnormal primary motor cortex morphology		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1315894	Btbd9	BTB domain containing 9	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1315894	Btbd9	BTB domain containing 9	gene	MP:0014254	increased paired-pulse ratio		IAGP		N	RGD:5509061	20230706	MGI			PMID:22536397
1315894	Btbd9	BTB domain containing 9	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:32446853
1315894	Btbd9	BTB domain containing 9	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:31715135
1315894	Btbd9	BTB domain containing 9	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:32446853
1315894	Btbd9	BTB domain containing 9	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22678064
1315894	Btbd9	BTB domain containing 9	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:32446853
1315897	Ptov1	prostate tumor over expressed gene 1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20221215	MGI			
1315897	Ptov1	prostate tumor over expressed gene 1	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20221215	MGI			
1315897	Ptov1	prostate tumor over expressed gene 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1315897	Ptov1	prostate tumor over expressed gene 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20221215	MGI			
1315897	Ptov1	prostate tumor over expressed gene 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20221215	MGI			
1315897	Ptov1	prostate tumor over expressed gene 1	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20221215	MGI			
1315897	Ptov1	prostate tumor over expressed gene 1	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20221215	MGI			
1315897	Ptov1	prostate tumor over expressed gene 1	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20221215	MGI			
1315897	Ptov1	prostate tumor over expressed gene 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1315899	C1qtnf7	C1q and tumor necrosis factor related protein 7	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20180315	MGI			PMID:28223291
1315899	C1qtnf7	C1q and tumor necrosis factor related protein 7	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1315899	C1qtnf7	C1q and tumor necrosis factor related protein 7	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180315	MGI			PMID:28223291
1315899	C1qtnf7	C1q and tumor necrosis factor related protein 7	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20180315	MGI			PMID:28223291
1315899	C1qtnf7	C1q and tumor necrosis factor related protein 7	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20180315	MGI			PMID:28223291
1315899	C1qtnf7	C1q and tumor necrosis factor related protein 7	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20180315	MGI			PMID:28223291
1315899	C1qtnf7	C1q and tumor necrosis factor related protein 7	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1315899	C1qtnf7	C1q and tumor necrosis factor related protein 7	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20260402	MGI			
1315899	C1qtnf7	C1q and tumor necrosis factor related protein 7	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
1315901	Ankrd60	ankyrin repeat domain 60	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1315901	Ankrd60	ankyrin repeat domain 60	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1315903	Piwil1	piwi-like RNA-mediated gene silencing 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22121019
1315903	Piwil1	piwi-like RNA-mediated gene silencing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062093
1315903	Piwil1	piwi-like RNA-mediated gene silencing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22121019
1315903	Piwil1	piwi-like RNA-mediated gene silencing 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062093
1315903	Piwil1	piwi-like RNA-mediated gene silencing 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22121019
1315903	Piwil1	piwi-like RNA-mediated gene silencing 1	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062093
1315903	Piwil1	piwi-like RNA-mediated gene silencing 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22121019
1315903	Piwil1	piwi-like RNA-mediated gene silencing 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062093
1315903	Piwil1	piwi-like RNA-mediated gene silencing 1	gene	MP:0031620	abnormal chromatoid body morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:22121019
1315907	Cfl2	cofilin 2, muscle	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315907	Cfl2	cofilin 2, muscle	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343409
1315908	Tmem165	transmembrane protein 165	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20160804	MGI			
1315908	Tmem165	transmembrane protein 165	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1315910	Btn1a1	butyrophilin, subfamily 1, member A1	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226505
1315910	Btn1a1	butyrophilin, subfamily 1, member A1	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226505
1315910	Btn1a1	butyrophilin, subfamily 1, member A1	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226505
1315912	Bcl2l13	BCL2 like 13	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240229	MGI			PMID:36608143
1315912	Bcl2l13	BCL2 like 13	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0006039	decreased mitochondrial fission		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0014246	decreased cellular ATP level		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315912	Bcl2l13	BCL2 like 13	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20250925	MGI			PMID:39580803
1315913	Ttc29	tetratricopeptide repeat domain 29	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:31735294
1315913	Ttc29	tetratricopeptide repeat domain 29	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:31735294
1315913	Ttc29	tetratricopeptide repeat domain 29	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:31735294
1315913	Ttc29	tetratricopeptide repeat domain 29	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31735294
1315913	Ttc29	tetratricopeptide repeat domain 29	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31735294
1315913	Ttc29	tetratricopeptide repeat domain 29	gene	MP:0009837	abnormal sperm end piece morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31735294
1315913	Ttc29	tetratricopeptide repeat domain 29	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20230601	MGI			
1315913	Ttc29	tetratricopeptide repeat domain 29	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20200310	MGI			PMID:31735294
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210520	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210520	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210826	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175329
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175329
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254996
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1315917	Chst2	carbohydrate sulfotransferase 2	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20210520	MGI			
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682947
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701168
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15280420
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8275084
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15280420
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466203
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466203
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682947
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701168
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701168
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466203
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466203
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466203
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713303
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701168
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466203
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713303
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8275084
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0003325	decreased liver function		IAGP		N	RGD:5509061	20141003	MGI			PMID:8275084
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713303
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713303
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8275084
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713303
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8275084
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:22257940
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682947
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20200206	MGI			PMID:22257940
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701168
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15280420
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15280420
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20200206	MGI			PMID:22257940
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466203
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200206	MGI			PMID:22257940
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701168
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701168
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682947
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8275084
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15280420
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8275084
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682947
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183314
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9197240
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0011126	absent primary ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:12466203
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200206	MGI			PMID:22257940
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:11713303
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:22701168
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0013705	decreased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:22701168
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0014645	decreased optokinetic reflex		IAGP		N	RGD:5509061	20250306	MGI			PMID:22257940
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0014694	anisokaryosis		IAGP		N	RGD:5509061	20250710	MGI			PMID:8275084
1315922	Ercc1	excision repair cross-complementing rodent repair deficiency, complementation group 1	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20200206	MGI			PMID:22257940
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20160804	MGI			
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19068231
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20160804	MGI			
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19068231
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0002074	abnormal hair texture		IEA		N	RGD:5509061	20160804	MGI			
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19068231
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19068231
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19068231
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1315924	Rad18	RAD18 E3 ubiquitin protein ligase	gene	MP:0010679	abnormal arrector pilli muscle morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1315928	Psme3	proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10608895
1315928	Psme3	proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10608895
1315928	Psme3	proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004203
1315928	Psme3	proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004203
1315928	Psme3	proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20260423	MGI			PMID:41372189
1315928	Psme3	proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004203
1315928	Psme3	proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004203
1315928	Psme3	proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)	gene	MP:0010283	decreased classified tumor incidence		IAGP		N	RGD:5509061	20260423	MGI			PMID:41372189
1315928	Psme3	proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki)	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004203
1315931	Thsd1	thrombospondin, type I, domain 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160421	MGI			
1315931	Thsd1	thrombospondin, type I, domain 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20170105	MGI			
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20181227	MGI			
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20221215	MGI			
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0010318	increased salivary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0010799	stomach mucosa hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123197
1315933	Gpx7	glutathione peroxidase 7	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:23123197
1315935	Fcsk	fucose kinase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1315947	Dcun1d5	defective in cullin neddylation 1 domain containing 5	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20210826	MGI			
1315947	Dcun1d5	defective in cullin neddylation 1 domain containing 5	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20221215	MGI			
1315947	Dcun1d5	defective in cullin neddylation 1 domain containing 5	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
1315951	Fxr2	FMR1 autosomal homolog 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875043
1315951	Fxr2	FMR1 autosomal homolog 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875043
1315951	Fxr2	FMR1 autosomal homolog 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875043
1315951	Fxr2	FMR1 autosomal homolog 2	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875043
1315951	Fxr2	FMR1 autosomal homolog 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875043
1315951	Fxr2	FMR1 autosomal homolog 2	gene	MP:0003460	decreased fear-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875043
1315951	Fxr2	FMR1 autosomal homolog 2	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875043
1315951	Fxr2	FMR1 autosomal homolog 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315951	Fxr2	FMR1 autosomal homolog 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:11875043
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000071	axial skeleton hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:6119797
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1269836
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7202842
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:6151297
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6151297
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:67117
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20230601	MGI			
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:624676
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:67117
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:1269836
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882565
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6151297
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:67117
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:858816
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671738
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:67117
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:6151297
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:67117
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:858816
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20230601	MGI			
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671738
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:8835524
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:67117
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:858816
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:6151297
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713631
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:858816
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0009908	protruding tongue		IEA		N	RGD:5509061	20230601	MGI			
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1315953	Papss2	3'-phosphoadenosine 5'-phosphosulfate synthase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20230119	MGI			
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003158	dysphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003252	abnormal bile duct physiology		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003769	abnormal lip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0009581	decreased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0009877	exostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0010293	increased integument system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0010297	increased hepatobiliary system tumor incidence		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0010315	increased cholangiocarcinoma incidence		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0010318	increased salivary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0011686	increased epidermal stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143302
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0012236	abnormal cholangiocyte morphology		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0013119	abdomen swellings		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0014038	increased hepatocyte number		IAGP		N	RGD:5509061	20170601	MGI			PMID:26699479
1315957	Mob1a	MOB kinase activator 1A	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:23143302
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20231207	MGI			
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0000392	accelerated hair follicle regression		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0000674	abnormal sweat gland morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0000763	abnormal filiform papillae morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20231207	MGI			
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:25629078
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0003931	absent molars		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:25629078
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:25629078
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0006257	abnormal fungiform papillae morphology		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0006260	abnormal gustatory papilla taste bud morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20170119	MGI			PMID:25629078
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0010773	supernumerary molars		IAGP		N	RGD:5509061	20170119	MGI			PMID:25629078
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0010773	supernumerary molars		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0011194	abnormal hair follicle physiology		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0013371	hypohidrosis		IAGP		N	RGD:5509061	20170810	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0030451	abnormal dentin mineralization		IAGP		N	RGD:5509061	20180215	MGI			PMID:25629078
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:25629078
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0030491	dental pulp stones		IAGP		N	RGD:5509061	20171228	MGI			PMID:25629078
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0030494	abnormal molar root morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:28589954
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0030496	taurodontia		IAGP		N	RGD:5509061	20171228	MGI			PMID:25629078
1315959	Wnt10a	wingless-type MMTV integration site family, member 10A	gene	MP:0030524	abnormal tooth root resorption		IAGP		N	RGD:5509061	20180118	MGI			PMID:25629078
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20190815	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15328404
1315961	Plscr3	phospholipid scramblase 3	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:15328404
1315964	Niban2	niban apoptosis regulator 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1315968	Poldip2	polymerase (DNA-directed), delta interacting protein 2	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825363
1315968	Poldip2	polymerase (DNA-directed), delta interacting protein 2	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825363
1315968	Poldip2	polymerase (DNA-directed), delta interacting protein 2	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825363
1315968	Poldip2	polymerase (DNA-directed), delta interacting protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825363
1315968	Poldip2	polymerase (DNA-directed), delta interacting protein 2	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825363
1315968	Poldip2	polymerase (DNA-directed), delta interacting protein 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825363
1315968	Poldip2	polymerase (DNA-directed), delta interacting protein 2	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825363
1315968	Poldip2	polymerase (DNA-directed), delta interacting protein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23825363
1315968	Poldip2	polymerase (DNA-directed), delta interacting protein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220106	MGI			PMID:34928942
1315970	Rhot1	ras homolog family member T1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0001391	abnormal tail movements		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315970	Rhot1	ras homolog family member T1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1315970	Rhot1	ras homolog family member T1	gene	MP:0012051	spasticity		IAGP		N	RGD:5509061	20150402	MGI			PMID:25136135
1315970	Rhot1	ras homolog family member T1	gene	MP:0014345	abnormal neuron mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:27705781
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20161201	MGI			
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20161201	MGI			
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002491	decreased IgD level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002533	abnormal type III hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210128	MGI			
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20161201	MGI			
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0005265	abnormal blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371362
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371362
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371362
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008185	decreased naive B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9806640
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0012361	decreased large unstained cell number		IEA		N	RGD:5509061	20161201	MGI			
1315972	Ikzf3	IKAROS family zinc finger 3	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:12574333
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20170223	MGI			PMID:22374166
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20170223	MGI			PMID:22374166
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0003968	abnormal growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20170223	MGI			PMID:22374166
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20170223	MGI			PMID:22374166
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0011924	abnormal liver zinc level		IAGP		N	RGD:5509061	20170223	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0011924	abnormal liver zinc level		IAGP		N	RGD:5509061	20170223	MGI			PMID:22374166
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20170223	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20170223	MGI			PMID:21445361
1315976	Slc39a14	solute carrier family 39 (zinc transporter), member 14	gene	MP:0030126	torticollis		IAGP		N	RGD:5509061	20171005	MGI			PMID:21445361
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315980	Gfus	GDP-L-fucose synthase	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12186857
1315984	Strn4	striatin, calmodulin binding protein 4	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20241121	MGI			
1315984	Strn4	striatin, calmodulin binding protein 4	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230119	MGI			
1315984	Strn4	striatin, calmodulin binding protein 4	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1315984	Strn4	striatin, calmodulin binding protein 4	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
1315984	Strn4	striatin, calmodulin binding protein 4	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1315984	Strn4	striatin, calmodulin binding protein 4	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1315984	Strn4	striatin, calmodulin binding protein 4	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230119	MGI			
1315984	Strn4	striatin, calmodulin binding protein 4	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20230119	MGI			
1315984	Strn4	striatin, calmodulin binding protein 4	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230119	MGI			
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20231207	MGI			
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106877
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106877
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884661
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002607	decreased basophil cell number		IEA		N	RGD:5509061	20250508	MGI			
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0002952	ventricular cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106877
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0003211	abnormal aorta elastic fiber morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0003305	proctitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0004882	enlarged lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0009310	increased large intestine adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884661
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0010052	increased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884661
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884661
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106877
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0010900	abnormal pulmonary interalveolar septum morphology		IAGP		N	RGD:5509061	20240704	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208849
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150709	MGI			PMID:25713297
1315989	Ltbp4	latent transforming growth factor beta binding protein 4	gene	MP:0021159	increased heart right ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:25713297
1315990	Fry	FRY microtubule binding protein	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1315990	Fry	FRY microtubule binding protein	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1315990	Fry	FRY microtubule binding protein	gene	MP:0004692	small pubis		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1315992	Cadm3	cell adhesion molecule 3	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19036974
1315993	Lypd8	LY6/PLAUR domain containing 8	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:27027293
1315993	Lypd8	LY6/PLAUR domain containing 8	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:27027293
1315993	Lypd8	LY6/PLAUR domain containing 8	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:27027293
1315993	Lypd8	LY6/PLAUR domain containing 8	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170323	MGI			
1315993	Lypd8	LY6/PLAUR domain containing 8	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20210415	MGI			PMID:27027293
1315993	Lypd8	LY6/PLAUR domain containing 8	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:27027293
1315993	Lypd8	LY6/PLAUR domain containing 8	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210415	MGI			PMID:27027293
1315993	Lypd8	LY6/PLAUR domain containing 8	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20210415	MGI			PMID:27027293
1315995	Tmc5	transmembrane channel-like gene family 5	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20220811	MGI			
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20181227	MGI			
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20210617	MGI			PMID:32796023
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20210617	MGI			PMID:32796023
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20210617	MGI			PMID:32796023
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20210617	MGI			PMID:32796023
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210617	MGI			PMID:32796023
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20210617	MGI			PMID:32796023
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0011078	increased macrophage cytokine production		IAGP		N	RGD:5509061	20210617	MGI			PMID:32796023
1315997	Dusp11	dual specificity phosphatase 11 (RNA/RNP complex 1-interacting)	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20160421	MGI			
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001705	abnormal proximal-distal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20220721	MGI			PMID:28319097
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0003085	abnormal egg cylinder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20190502	MGI			
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20201231	MGI			
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20211014	MGI			PMID:25417106
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20220721	MGI			PMID:28319097
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20211014	MGI			PMID:25417106
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0011190	thick embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0012159	absent anterior visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0012161	absent distal visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974875
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794365
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:28319097
1315999	Bptf	bromodomain PHD finger transcription factor	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:35604347
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618507
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876179
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618507
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618507
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876179
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22114267
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:22114267
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618507
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618507
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618507
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22114267
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875933
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618507
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9096336
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876179
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0012235	abnormal liver bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9618507
1316001	Map2k4	mitogen-activated protein kinase kinase 4	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:17875933
1316002	Pcid2	PCI domain containing 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
1316002	Pcid2	PCI domain containing 2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0002227	abnormal spleen capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870947
1316002	Pcid2	PCI domain containing 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870947
1316002	Pcid2	PCI domain containing 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870947
1316002	Pcid2	PCI domain containing 2	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870947
1316002	Pcid2	PCI domain containing 2	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339895
1316002	Pcid2	PCI domain containing 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200220	MGI			PMID:24167073
1316002	Pcid2	PCI domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1316002	Pcid2	PCI domain containing 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20260402	MGI			
1316002	Pcid2	PCI domain containing 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20260402	MGI			
1316002	Pcid2	PCI domain containing 2	gene	MP:0014078	small intestinal villus atrophy		IAGP		N	RGD:5509061	20160414	MGI			PMID:18339895
1316014	Helz	helicase with zinc finger domain	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471385
1316014	Helz	helicase with zinc finger domain	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316016	Steap2	six transmembrane epithelial antigen of prostate 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316016	Steap2	six transmembrane epithelial antigen of prostate 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1316017	Acss3	acyl-CoA synthetase short-chain family member 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1316017	Acss3	acyl-CoA synthetase short-chain family member 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20250508	MGI			
1316017	Acss3	acyl-CoA synthetase short-chain family member 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20250508	MGI			
1316017	Acss3	acyl-CoA synthetase short-chain family member 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20250508	MGI			
1316017	Acss3	acyl-CoA synthetase short-chain family member 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20250508	MGI			
1316017	Acss3	acyl-CoA synthetase short-chain family member 3	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20250508	MGI			
1316017	Acss3	acyl-CoA synthetase short-chain family member 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20250508	MGI			
1316017	Acss3	acyl-CoA synthetase short-chain family member 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1316020	Pus7	pseudouridylate synthase 7	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20220811	MGI			
1316020	Pus7	pseudouridylate synthase 7	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1316020	Pus7	pseudouridylate synthase 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0008975	delayed male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316023	Fhl5	four and a half LIM domains 5	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247423
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0005615	increased susceptibility to type III hypersensitivity reaction		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0011566	abnormal complement protein level		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316025	C1qtnf6	C1q and tumor necrosis factor related protein 6	gene	MP:0020217	increased circulating complement protein level		IAGP		N	RGD:5509061	20191031	MGI			PMID:26404464
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20241121	MGI			
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210128	MGI			
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20241121	MGI			
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20241121	MGI			
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0014424	increased liver triglyceride secretion		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0014425	decreased liver triglyceride secretion		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316027	C1qtnf12	C1q and tumor necrosis factor related 12	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20250626	MGI			PMID:27815536
1316029	Arhgef28	Rho guanine nucleotide exchange factor 28	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151112	MGI			PMID:22649559
1316029	Arhgef28	Rho guanine nucleotide exchange factor 28	gene	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20151112	MGI			PMID:22649559
1316029	Arhgef28	Rho guanine nucleotide exchange factor 28	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1316029	Arhgef28	Rho guanine nucleotide exchange factor 28	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20151112	MGI			PMID:22649559
1316029	Arhgef28	Rho guanine nucleotide exchange factor 28	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20151112	MGI			PMID:22649559
1316031	Rhog	ras homolog family member G	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701744
1316031	Rhog	ras homolog family member G	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701744
1316031	Rhog	ras homolog family member G	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701744
1316031	Rhog	ras homolog family member G	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701744
1316031	Rhog	ras homolog family member G	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701744
1316040	Snta1	syntrophin, acidic 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995443
1316040	Snta1	syntrophin, acidic 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548643
1316040	Snta1	syntrophin, acidic 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548643
1316040	Snta1	syntrophin, acidic 1	gene	MP:0001784	abnormal fluid regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578959
1316040	Snta1	syntrophin, acidic 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578959
1316040	Snta1	syntrophin, acidic 1	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995443
1316040	Snta1	syntrophin, acidic 1	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548643
1316040	Snta1	syntrophin, acidic 1	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578959
1316042	Abca8b	ATP-binding cassette, sub-family A member 8b	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20190411	MGI			PMID:28882873
1316042	Abca8b	ATP-binding cassette, sub-family A member 8b	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20190411	MGI			PMID:28882873
1316042	Abca8b	ATP-binding cassette, sub-family A member 8b	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20190411	MGI			PMID:28882873
1316042	Abca8b	ATP-binding cassette, sub-family A member 8b	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20190411	MGI			PMID:28882873
1316050	Cog8	component of oligomeric golgi complex 8	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1316050	Cog8	component of oligomeric golgi complex 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1316050	Cog8	component of oligomeric golgi complex 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1316052	Elp3	elongator acetyltransferase complex subunit 3	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20170608	MGI			PMID:26527802
1316052	Elp3	elongator acetyltransferase complex subunit 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20170427	MGI			PMID:27476491
1316052	Elp3	elongator acetyltransferase complex subunit 3	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20170608	MGI			PMID:26527802
1316052	Elp3	elongator acetyltransferase complex subunit 3	gene	MP:0010156	abnormal small intestinal crypt cell physiology		IAGP		N	RGD:5509061	20170608	MGI			PMID:26527802
1316052	Elp3	elongator acetyltransferase complex subunit 3	gene	MP:0012434	decreased intestinal adenoma incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:26527802
1316052	Elp3	elongator acetyltransferase complex subunit 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20170427	MGI			PMID:27476491
1316052	Elp3	elongator acetyltransferase complex subunit 3	gene	MP:0014353	abnormal gastrointestinal brush cell morphology		IAGP		N	RGD:5509061	20240104	MGI			PMID:26527802
1316052	Elp3	elongator acetyltransferase complex subunit 3	gene	MP:0014754	abnormal tumor progression		IAGP		N	RGD:5509061	20250925	MGI			PMID:26527802
1316052	Elp3	elongator acetyltransferase complex subunit 3	gene	MP:0031319	impaired intestine regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:26527802
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12963709
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0003462	abnormal response to novel odor		IAGP		N	RGD:5509061	20160310	MGI			PMID:26647347
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0014115	cognitive inflexibility		IAGP		N	RGD:5509061	20160317	MGI			PMID:26647347
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0014620	abnormal interictal brain wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0020340	abnormal inhibitory learning		IAGP		N	RGD:5509061	20160915	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:21962519
1316053	Cntnap2	contactin associated protein-like 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:26647347
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20260402	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470285
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001329	retina hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470285
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20241121	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20260402	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001714	absent trophoblast giant cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20260402	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0001785	edema		IEA		N	RGD:5509061	20260402	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20260402	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20241121	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20260402	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470285
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0010706	ventral rotation of lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470285
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0010715	retina coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470285
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0010717	optic nerve coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470285
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0011193	embryonic epiblast cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0012102	absent trophectoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055728
1316055	Rybp	RING1 and YY1 binding protein	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20260402	MGI			
1316059	Slc4a1ap	solute carrier family 4 (anion exchanger), member 1, adaptor protein	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1316059	Slc4a1ap	solute carrier family 4 (anion exchanger), member 1, adaptor protein	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20210128	MGI			
1316061	Pan3	PAN3 poly(A) specific ribonuclease subunit	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210128	MGI			
1316061	Pan3	PAN3 poly(A) specific ribonuclease subunit	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1316061	Pan3	PAN3 poly(A) specific ribonuclease subunit	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1316061	Pan3	PAN3 poly(A) specific ribonuclease subunit	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1316061	Pan3	PAN3 poly(A) specific ribonuclease subunit	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20210128	MGI			
1316061	Pan3	PAN3 poly(A) specific ribonuclease subunit	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1316063	Trp73	transformation related protein 73	gene	MP:0000344	absent Cajal-Retzius cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0000487	absent enterocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0000503	excessive digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805388
1316063	Trp73	transformation related protein 73	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22160706
1316063	Trp73	transformation related protein 73	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22160706
1316063	Trp73	transformation related protein 73	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805388
1316063	Trp73	transformation related protein 73	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805388
1316063	Trp73	transformation related protein 73	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0001355	submission towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0001788	periorbital edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001867	rhinitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001872	sinus inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001893	non-obstructive hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001911	abnormal cerebrospinal fluid production		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805388
1316063	Trp73	transformation related protein 73	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0001928	abnormal ovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0002243	abnormal vomeronasal organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0002243	abnormal vomeronasal organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805388
1316063	Trp73	transformation related protein 73	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805388
1316063	Trp73	transformation related protein 73	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805388
1316063	Trp73	transformation related protein 73	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260402	MGI			PMID:39201474
1316063	Trp73	transformation related protein 73	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0004684	intervertebral disk degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1316063	Trp73	transformation related protein 73	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20211021	MGI			
1316063	Trp73	transformation related protein 73	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1316063	Trp73	transformation related protein 73	gene	MP:0008031	decreased Cajal-Retzius cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805388
1316063	Trp73	transformation related protein 73	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22160706
1316063	Trp73	transformation related protein 73	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22160706
1316063	Trp73	transformation related protein 73	gene	MP:0008780	increased pancreatic acinar cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0009485	distended ileum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0009648	abnormal superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22160706
1316063	Trp73	transformation related protein 73	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1316063	Trp73	transformation related protein 73	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1316063	Trp73	transformation related protein 73	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716451
1316063	Trp73	transformation related protein 73	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194434
1316063	Trp73	transformation related protein 73	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316063	Trp73	transformation related protein 73	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0013537	increased salivary gland adenoma incidence		IAGP		N	RGD:5509061	20150219	MGI			PMID:15837625
1316063	Trp73	transformation related protein 73	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1316063	Trp73	transformation related protein 73	gene	MP:0014445	abnormal spindle assembly in female meiosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:18805989
1316063	Trp73	transformation related protein 73	gene	MP:0014592	decreased gonadotropin-releasing hormone neuron number		IAGP		N	RGD:5509061	20241212	MGI			PMID:19805388
1316063	Trp73	transformation related protein 73	gene	MP:0014746	abnormal hippocampal mossy fiber innervation pattern		IAGP		N	RGD:5509061	20250911	MGI			PMID:22160706
1316063	Trp73	transformation related protein 73	gene	MP:0020422	decreased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1316063	Trp73	transformation related protein 73	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:18805989
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191205	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20220519	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20211021	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210128	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20160804	MGI			
1316065	Ska2	spindle and kinetochore associated complex subunit 2	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1316067	Tm9sf1	transmembrane 9 superfamily member 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050391
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20151217	MGI			PMID:11260255
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050393
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11260255
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884603
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884603
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19204108
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:19204108
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22547703
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19204108
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22547703
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19204108
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22547703
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20220811	MGI			
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19204108
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19204108
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215524
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050393
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050391
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11260255
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884603
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0012509	neural tube degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050392
1316070	Rev3l	REV3 like, DNA directed polymerase zeta catalytic subunit	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20151217	MGI			PMID:11260255
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20200514	MGI			
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:31220454
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20201231	MGI			
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20240328	MGI			PMID:31220454
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20240328	MGI			PMID:31220454
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0004165	abnormal lateral geniculate nucleus morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:31220454
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20200514	MGI			
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20210520	MGI			
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20240328	MGI			PMID:31220454
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18952058
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:34208876
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20240328	MGI			PMID:27615440
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20240328	MGI			PMID:31220454
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20211021	MGI			
1316072	Hcar1	hydrocarboxylic acid receptor 1	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20240328	MGI			PMID:31220454
1316074	Ntng2	netrin G2	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17973922
1316074	Ntng2	netrin G2	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:17973922
1316076	Sbf1	SET binding factor 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20221215	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20210826	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994405
1316076	Sbf1	SET binding factor 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994405
1316076	Sbf1	SET binding factor 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220811	MGI			PMID:34718573
1316076	Sbf1	SET binding factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20220811	MGI			PMID:34718573
1316076	Sbf1	SET binding factor 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20220811	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220811	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994405
1316076	Sbf1	SET binding factor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220811	MGI			PMID:34718573
1316076	Sbf1	SET binding factor 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220811	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210826	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20220811	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994405
1316076	Sbf1	SET binding factor 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:34718573
1316076	Sbf1	SET binding factor 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20220811	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20220811	MGI			PMID:34718573
1316076	Sbf1	SET binding factor 1	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20220811	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994405
1316076	Sbf1	SET binding factor 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220811	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20210826	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994405
1316076	Sbf1	SET binding factor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220811	MGI			PMID:34718573
1316076	Sbf1	SET binding factor 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1316076	Sbf1	SET binding factor 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11994405
1316076	Sbf1	SET binding factor 1	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11994405
1316076	Sbf1	SET binding factor 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11994405
1316076	Sbf1	SET binding factor 1	gene	MP:0020452	abnormal axon radial sorting		IAGP		N	RGD:5509061	20220811	MGI			PMID:34718573
1316076	Sbf1	SET binding factor 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220811	MGI			
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0009488	abnormal pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316078	Tfb2m	transcription factor B2, mitochondrial	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20210805	MGI			PMID:28702322
1316079	Tmem169	transmembrane protein 169	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0014254	increased paired-pulse ratio		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0014379	decreased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316079	Tmem169	transmembrane protein 169	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1316081	Ppef2	protein phosphatase, EF hand calcium-binding domain 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713293
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0008276	failure of intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010587	conotruncal ridge hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010589	common truncal valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0010652	absent aorticopulmonary septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1316082	Pds5a	PDS5 cohesin associated factor A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1316084	Rab5c	RAB5C, member RAS oncogene family	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1316084	Rab5c	RAB5C, member RAS oncogene family	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1316084	Rab5c	RAB5C, member RAS oncogene family	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1316084	Rab5c	RAB5C, member RAS oncogene family	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1316084	Rab5c	RAB5C, member RAS oncogene family	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20230601	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210128	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20210128	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20220519	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0008443	absent subplate		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231130	MGI			PMID:30428088
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0011724	ectopic cortical neuron		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0012139	increased forebrain size		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0014558	decreased cortical ventricular zone thickness		IAGP		N	RGD:5509061	20241031	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0020067	increased neocortex size		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316087	Wdfy3	WD repeat and FYVE domain containing 3	gene	MP:0020389	increased radial glial cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25198012
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436615
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596243
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436615
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197710
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436615
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596243
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955448
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318233
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31305241
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436615
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:24423059
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955448
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197710
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596243
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318233
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318233
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318233
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210822
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22295099
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596243
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596243
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955448
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436615
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955448
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596243
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691547
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210822
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0002913	abnormal PNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0003631	nervous system phenotype		IAGP		N	RGD:5509061	20250605	MGI			PMID:22318233
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0003647	absent oligodendrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318233
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24179156
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955448
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691547
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210822
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20220324	MGI			PMID:35022234
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22295099
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009684	abnormal spinal cord lateral motor column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009684	abnormal spinal cord lateral motor column morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:31305241
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009685	abnormal spinal cord motor column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009686	abnormal spinal cord medial motor column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20220324	MGI			PMID:35022234
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0010160	increased oligodendrocyte number		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596243
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826664
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121626
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955448
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20220324	MGI			PMID:35022234
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0021103	abnormal ventral interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:11955447
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:11955448
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:22036570
1316089	Olig2	oligodendrocyte transcription factor 2	gene	MP:0031496	motor developmental delay		IAGP		N	RGD:5509061	20250515	MGI			PMID:34583988
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20141003	MGI			
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0003330	abnormal auditory tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0006018	abnormal tympanic membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0009891	abnormal palate bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0011087	neonatal lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0020900	abnormal middle ear epithelium morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0020903	increased middle ear goblet cell number		IAGP		N	RGD:5509061	20191219	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0030154	abnormal tympanic cavity morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0030226	middle ear polyps		IAGP		N	RGD:5509061	20171019	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0030410	middle ear effusion		IAGP		N	RGD:5509061	20171207	MGI			PMID:18219393
1316091	Eya4	EYA transcriptional coactivator and phosphatase 4	gene	MP:0030413	tympanic membrane retraction		IAGP		N	RGD:5509061	20171207	MGI			PMID:18219393
1316094	Lmo2	LIM domain only 2	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1316094	Lmo2	LIM domain only 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1316094	Lmo2	LIM domain only 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1316094	Lmo2	LIM domain only 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1316094	Lmo2	LIM domain only 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1316094	Lmo2	LIM domain only 2	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10618416
1316094	Lmo2	LIM domain only 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1316094	Lmo2	LIM domain only 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1316094	Lmo2	LIM domain only 2	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1316094	Lmo2	LIM domain only 2	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0003794	delayed somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1316094	Lmo2	LIM domain only 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1316094	Lmo2	LIM domain only 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0012131	small visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8033210
1316094	Lmo2	LIM domain only 2	gene	MP:0013657	abnormal blood cell morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:19966810
1316094	Lmo2	LIM domain only 2	gene	MP:0013705	decreased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:19966810
1316098	Prpf6	pre-mRNA splicing factor 6	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1316098	Prpf6	pre-mRNA splicing factor 6	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1316098	Prpf6	pre-mRNA splicing factor 6	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1316098	Prpf6	pre-mRNA splicing factor 6	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20170105	MGI			
1316098	Prpf6	pre-mRNA splicing factor 6	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1316098	Prpf6	pre-mRNA splicing factor 6	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1316098	Prpf6	pre-mRNA splicing factor 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316098	Prpf6	pre-mRNA splicing factor 6	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1316103	Ankrd27	ankyrin repeat domain 27	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20260402	MGI			
1316103	Ankrd27	ankyrin repeat domain 27	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20160421	MGI			
1316103	Ankrd27	ankyrin repeat domain 27	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20160421	MGI			
1316104	Pigz	phosphatidylinositol glycan anchor biosynthesis, class Z	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1316104	Pigz	phosphatidylinositol glycan anchor biosynthesis, class Z	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210826	MGI			
1316104	Pigz	phosphatidylinositol glycan anchor biosynthesis, class Z	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210826	MGI			
1316108	Ndufs2	NADH:ubiquinone oxidoreductase core subunit S2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1316108	Ndufs2	NADH:ubiquinone oxidoreductase core subunit S2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1316108	Ndufs2	NADH:ubiquinone oxidoreductase core subunit S2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316108	Ndufs2	NADH:ubiquinone oxidoreductase core subunit S2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1316114	Fignl1	fidgetin-like 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20231123	MGI			PMID:37891173
1316114	Fignl1	fidgetin-like 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20231123	MGI			PMID:37891173
1316114	Fignl1	fidgetin-like 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20231123	MGI			PMID:37891173
1316114	Fignl1	fidgetin-like 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20231123	MGI			PMID:37891173
1316114	Fignl1	fidgetin-like 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20231123	MGI			PMID:37891173
1316114	Fignl1	fidgetin-like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316116	Zfand3	zinc finger, AN1-type domain 3	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1316116	Zfand3	zinc finger, AN1-type domain 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1316116	Zfand3	zinc finger, AN1-type domain 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1316116	Zfand3	zinc finger, AN1-type domain 3	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20231207	MGI			
1316116	Zfand3	zinc finger, AN1-type domain 3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20260402	MGI			
1316116	Zfand3	zinc finger, AN1-type domain 3	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1316116	Zfand3	zinc finger, AN1-type domain 3	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1316116	Zfand3	zinc finger, AN1-type domain 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1316118	Ndufb9	NADH:ubiquinone oxidoreductase subunit B9	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1316118	Ndufb9	NADH:ubiquinone oxidoreductase subunit B9	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1316118	Ndufb9	NADH:ubiquinone oxidoreductase subunit B9	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1316118	Ndufb9	NADH:ubiquinone oxidoreductase subunit B9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316120	Cenpe	centromere protein E	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1316120	Cenpe	centromere protein E	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1316120	Cenpe	centromere protein E	gene	MP:0002658	abnormal liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361599
1316120	Cenpe	centromere protein E	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361599
1316120	Cenpe	centromere protein E	gene	MP:0004966	abnormal inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361599
1316120	Cenpe	centromere protein E	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361599
1316120	Cenpe	centromere protein E	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361599
1316120	Cenpe	centromere protein E	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316120	Cenpe	centromere protein E	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1316120	Cenpe	centromere protein E	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1316123	Cxcl11	chemokine (C-X-C motif) ligand 11	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20240418	MGI			PMID:35233830
1316123	Cxcl11	chemokine (C-X-C motif) ligand 11	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240418	MGI			PMID:35233830
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20181018	MGI			PMID:29428562
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210826	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20190502	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0001127	small ovary		IEA		N	RGD:5509061	20210826	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20231207	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20181018	MGI			PMID:29428562
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20181227	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:29428562
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:29428562
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002284	abnormal tracheal smooth muscle morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:29428562
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20210826	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:29428562
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0003933	abnormal cementum morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0004551	decreased tracheal cartilage ring number		IAGP		N	RGD:5509061	20181018	MGI			PMID:29428562
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20240523	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0010883	trachea stenosis		IAGP		N	RGD:5509061	20181018	MGI			PMID:29428562
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0013251	dental pulp necrosis		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0013496	abnormal trachea development		IAGP		N	RGD:5509061	20181018	MGI			PMID:29428562
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0013623	increased femur compact bone thickness		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20190530	MGI			PMID:30622831
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0030101	carious teeth		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0030132	periodontium inflammation		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0030453	abnormal odontoblast morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0030463	apical tooth abscess		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0030494	abnormal molar root morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316125	Notum	notum palmitoleoyl-protein carboxylesterase	gene	MP:0030542	abnormal dentin development		IAGP		N	RGD:5509061	20190530	MGI			PMID:26926082
1316127	Snrnp70	small nuclear ribonucleoprotein 70 (U1)	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1316127	Snrnp70	small nuclear ribonucleoprotein 70 (U1)	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241017	MGI			
1316127	Snrnp70	small nuclear ribonucleoprotein 70 (U1)	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1316127	Snrnp70	small nuclear ribonucleoprotein 70 (U1)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20221215	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220811	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20221215	MGI			
1316130	Zc2hc1c	zinc finger, C2HC-type containing 1C	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20220811	MGI			
1316131	Pcdhb9	protocadherin beta 9	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1316131	Pcdhb9	protocadherin beta 9	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1316131	Pcdhb9	protocadherin beta 9	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20230601	MGI			
1316132	Ankrd52	ankyrin repeat domain 52	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1316132	Ankrd52	ankyrin repeat domain 52	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1316132	Ankrd52	ankyrin repeat domain 52	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1316132	Ankrd52	ankyrin repeat domain 52	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1316132	Ankrd52	ankyrin repeat domain 52	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210128	MGI			
1316132	Ankrd52	ankyrin repeat domain 52	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1316132	Ankrd52	ankyrin repeat domain 52	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200402	MGI			
1316132	Ankrd52	ankyrin repeat domain 52	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316134	Kctd11	potassium channel tetramerisation domain containing 11	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1316134	Kctd11	potassium channel tetramerisation domain containing 11	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1316145	Slco5a1	solute carrier organic anion transporter family, member 5A1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20260402	MGI			
1316147	Lamtor3	late endosomal/lysosomal adaptor, MAPK and MTOR activator 3	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20230119	MGI			
1316147	Lamtor3	late endosomal/lysosomal adaptor, MAPK and MTOR activator 3	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20230119	MGI			
1316147	Lamtor3	late endosomal/lysosomal adaptor, MAPK and MTOR activator 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1316150	Zfp42	zinc finger protein 42	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316150	Zfp42	zinc finger protein 42	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21233130
1316150	Zfp42	zinc finger protein 42	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641340
1316150	Zfp42	zinc finger protein 42	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1316150	Zfp42	zinc finger protein 42	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641340
1316150	Zfp42	zinc finger protein 42	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:21233130
1316150	Zfp42	zinc finger protein 42	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641340
1316150	Zfp42	zinc finger protein 42	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20201022	MGI			
1316150	Zfp42	zinc finger protein 42	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18433507
1316150	Zfp42	zinc finger protein 42	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21233130
1316150	Zfp42	zinc finger protein 42	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641340
1316150	Zfp42	zinc finger protein 42	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641340
1316150	Zfp42	zinc finger protein 42	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21233130
1316150	Zfp42	zinc finger protein 42	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21233130
1316150	Zfp42	zinc finger protein 42	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1316152	Zfp367	zinc finger protein 367	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20160804	MGI			
1316153	Shc2	SHC (Src homology 2 domain containing) transforming protein 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163269
1316153	Shc2	SHC (Src homology 2 domain containing) transforming protein 2	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163269
1316153	Shc2	SHC (Src homology 2 domain containing) transforming protein 2	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163269
1316153	Shc2	SHC (Src homology 2 domain containing) transforming protein 2	gene	MP:0000969	abnormal nociceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163269
1316153	Shc2	SHC (Src homology 2 domain containing) transforming protein 2	gene	MP:0001015	small superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163269
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20201022	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20190502	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20170406	MGI			PMID:23300183
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000418	focal hair loss		IEA		N	RGD:5509061	20161201	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20190502	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20190502	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001586	abnormal erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001670	abnormal intestinal mineral absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001923	reduced female fertility		IEA		N	RGD:5509061	20111116	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20190502	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002224	abnormal spleen size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20170406	MGI			PMID:23300183
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20170406	MGI			PMID:23300183
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0003582	abnormal ovary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20170406	MGI			PMID:23300183
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20201022	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20170406	MGI			PMID:23300183
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20170406	MGI			PMID:23300183
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20201022	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201022	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008738	abnormal liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008739	abnormal spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20170406	MGI			PMID:23300183
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0009004	progressive hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451267
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20190502	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0010682	abnormal hair follicle infundibulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0010689	thin hair follicle outer root sheath		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523150
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201022	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0011284	abnormal circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0011896	increased circulating unsaturated transferrin level		IAGP		N	RGD:5509061	20170406	MGI			PMID:23300183
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20190502	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0013302	increased pancreas iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0013303	decreased pancreas iron level		IAGP		N	RGD:5509061	20161020	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0013510	decreased CD4-negative NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0013514	increased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0013648	increased CD11b-high dendritic cell number		IEA		N	RGD:5509061	20211021	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0013670	increased Ly6C-positive immature NK cell number		IEA		N	RGD:5509061	20260402	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0013676	increased Ly6C-positive mature NK cell number		IEA		N	RGD:5509061	20201022	MGI			
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0014990	enhanced erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:22490684
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0020367	increased heart iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0020368	decreased heart iron level		IAGP		N	RGD:5509061	20161020	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0031692	decreased muscle iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:20200349
1316155	Tmprss6	transmembrane serine protease 6	gene	MP:0031693	increased muscle iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:20200349
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0004143	muscle hypertonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20170105	MGI			
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841728
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170105	MGI			
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316157	Ercc3	excision repair cross-complementing rodent repair deficiency, complementation group 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:19321664
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20150129	MGI			PMID:25124451
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0004525	thin cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20150129	MGI			PMID:25124451
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:25124451
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0004528	fused outer hair cell stereocilia		IAGP		N	RGD:5509061	20150129	MGI			PMID:25124451
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:25124451
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0004534	decreased inner hair cell stereocilia number		IAGP		N	RGD:5509061	20150129	MGI			PMID:25124451
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0004536	short inner hair cell stereocilia		IAGP		N	RGD:5509061	20150129	MGI			PMID:25124451
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20150129	MGI			PMID:25124451
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0008141	decreased small intestinal microvillus size		IAGP		N	RGD:5509061	20150129	MGI			PMID:19321664
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20150129	MGI			PMID:19321664
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20150129	MGI			PMID:19321664
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20150129	MGI			PMID:19321664
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20150129	MGI			PMID:25124451
1316160	Pls1	plastin 1 (I-isoform)	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20150129	MGI			PMID:19321664
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19617532
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19617532
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19617532
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0010747	abnormal enamel organ morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0030083	long upper incisors		IAGP		N	RGD:5509061	20180125	MGI			PMID:19622764
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20180125	MGI			PMID:19617532
1316163	Antxr1	anthrax toxin receptor 1	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20180125	MGI			PMID:19622764
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316167	Dusp22	dual specificity phosphatase 22	gene	MP:0011567	increased renal glomerulus lobularity		IAGP		N	RGD:5509061	20191226	MGI			PMID:24714587
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141211	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20111116	MGI			
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200910	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001577	anemia		IEA		N	RGD:5509061	20111116	MGI			
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20200910	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141211	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20200910	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001924	infertility		IEA		N	RGD:5509061	20111116	MGI			
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141211	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141211	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141211	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002959	increased urine microalbumin level		IAGP		N	RGD:5509061	20141211	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0003381	vitreal fibroplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141211	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0006203	eye hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0009026	abnormal brain pia mater morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0009275	bruising		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20141211	MGI			PMID:16598045
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0010235	abnormal retina inner limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0010252	anterior subcapsular cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0010259	anterior polar cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0010261	sutural cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011187	abnormal parietal endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011419	erythrocyturia		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011498	abnormal glomerular capsule parietal layer morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011502	parietal capsular epithelium metaplasia		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0011843	abnormal kidney collecting duct epithelium morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:21625620
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0020153	abnormal urine albumin level		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20170803	MGI			PMID:26260163
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:15905400
1316171	Col4a1	collagen, type IV, alpha 1	gene	MP:0031109	subarachnoid hemorrhage		IAGP		N	RGD:5509061	20200910	MGI			PMID:16598045
1316173	Spink8	serine peptidase inhibitor, Kazal type 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1316179	Mettl26	methyltransferase like 26	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1316179	Mettl26	methyltransferase like 26	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1316181	Pigt	phosphatidylinositol glycan anchor biosynthesis, class T	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170413	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20230601	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230601	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230601	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1316184	Ccdc186	coiled-coil domain containing 186	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316186	Sf3b2	splicing factor 3b, subunit 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1316186	Sf3b2	splicing factor 3b, subunit 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1316186	Sf3b2	splicing factor 3b, subunit 2	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1316186	Sf3b2	splicing factor 3b, subunit 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1316186	Sf3b2	splicing factor 3b, subunit 2	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1316186	Sf3b2	splicing factor 3b, subunit 2	gene	MP:0021088	impaired spatial memory extinction		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1316191	Glyat	glycine-N-acyltransferase	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20250508	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20241121	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20220519	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313413
1316193	Tyk2	tyrosine kinase 2	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20220519	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220519	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070174
1316193	Tyk2	tyrosine kinase 2	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070174
1316193	Tyk2	tyrosine kinase 2	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14617019
1316193	Tyk2	tyrosine kinase 2	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20250508	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313413
1316193	Tyk2	tyrosine kinase 2	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148148
1316193	Tyk2	tyrosine kinase 2	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148148
1316193	Tyk2	tyrosine kinase 2	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313414
1316193	Tyk2	tyrosine kinase 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313413
1316193	Tyk2	tyrosine kinase 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14617019
1316193	Tyk2	tyrosine kinase 2	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IEA		N	RGD:5509061	20220519	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313413
1316193	Tyk2	tyrosine kinase 2	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313413
1316193	Tyk2	tyrosine kinase 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070173
1316193	Tyk2	tyrosine kinase 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070174
1316193	Tyk2	tyrosine kinase 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313413
1316193	Tyk2	tyrosine kinase 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313414
1316193	Tyk2	tyrosine kinase 2	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313414
1316193	Tyk2	tyrosine kinase 2	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070174
1316193	Tyk2	tyrosine kinase 2	gene	MP:0009791	increased susceptibility to viral infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070173
1316193	Tyk2	tyrosine kinase 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0010895	increased lung compliance		IEA		N	RGD:5509061	20260402	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0011077	decreased macrophage nitric oxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070173
1316193	Tyk2	tyrosine kinase 2	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217260
1316193	Tyk2	tyrosine kinase 2	gene	MP:0011971	increased circulating lactate dehydrogenase level		IEA		N	RGD:5509061	20241121	MGI			
1316193	Tyk2	tyrosine kinase 2	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11070173
1316193	Tyk2	tyrosine kinase 2	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16148148
1316193	Tyk2	tyrosine kinase 2	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:22723949
1316193	Tyk2	tyrosine kinase 2	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:16148148
1316193	Tyk2	tyrosine kinase 2	gene	MP:0031040	increased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:22723949
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201231	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20210128	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20201231	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201231	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20230601	MGI			
1316199	Leprotl1	leptin receptor overlapping transcript-like 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1316204	Ahsa2	AHA1, activator of heat shock protein ATPase 2	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210826	MGI			
1316204	Ahsa2	AHA1, activator of heat shock protein ATPase 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1316205	Got1l1	glutamic-oxaloacetic transaminase 1-like 1	gene	MP:0030707	decreased glutamine level		IAGP		N	RGD:5509061	20210415	MGI			PMID:25287256
1316205	Got1l1	glutamic-oxaloacetic transaminase 1-like 1	gene	MP:0030737	decreased glutamic acid level		IAGP		N	RGD:5509061	20210415	MGI			PMID:25287256
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540762
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577581
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540762
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142808
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577581
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142808
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577581
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577581
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142808
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540762
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577581
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142808
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540762
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0004781	abnormal surfactant composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540762
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577581
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142808
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577581
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577581
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010814	absent alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142808
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010814	absent alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010814	absent alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540762
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010817	absent type I pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142808
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540762
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010897	abnormal bronchiole epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0010909	pulmonary alveolar hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142808
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142808
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540762
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577581
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540762
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316208	Abca3	ATP-binding cassette, sub-family A member 3	gene	MP:0011163	increased wet-to-dry lung weight ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267394
1316211	Dpt	dermatopontin	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230512
1316211	Dpt	dermatopontin	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230512
1316211	Dpt	dermatopontin	gene	MP:0003092	decreased cornea stroma thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877395
1316211	Dpt	dermatopontin	gene	MP:0003094	abnormal cornea posterior stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877395
1316211	Dpt	dermatopontin	gene	MP:0005275	abnormal skin tensile strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230512
1316211	Dpt	dermatopontin	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877395
1316211	Dpt	dermatopontin	gene	MP:0005421	loose skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230512
1316211	Dpt	dermatopontin	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877395
1316211	Dpt	dermatopontin	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230512
1316211	Dpt	dermatopontin	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230512
1316213	Jakmip3	janus kinase and microtubule interacting protein 3	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20240523	MGI			
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001491	unresponsive to tactile stimuli		IEA		N	RGD:5509061	20210520	MGI			
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0004167	abnormal cingulate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0008534	enlarged fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0010856	dilated respiratory conducting tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0010935	increased airway resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0011012	bronchiectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0011026	impaired branching involved in trachea morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19581591
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0012489	abnormal retrosplenial region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16190882
1316219	Npas3	neuronal PAS domain protein 3	gene	MP:0031442	enlarged cerebral aqueduct		IAGP		N	RGD:5509061	20221103	MGI			PMID:16190882
1316220	Treml6	triggering receptor expressed on myeloid cells-like 6	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20260402	MGI			
1316220	Treml6	triggering receptor expressed on myeloid cells-like 6	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20260402	MGI			
1316220	Treml6	triggering receptor expressed on myeloid cells-like 6	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20210520	MGI			
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20240523	MGI			
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0003908	decreased stereotypic behavior		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:30673609
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20250508	MGI			
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200514	MGI			
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20210415	MGI			PMID:30673609
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1316226	Cbarp	calcium channel, voltage-dependent, beta subunit associated regulatory protein	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20210506	MGI			PMID:26136667
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002219	decreased lymph node number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002343	abnormal lymph node cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002364	abnormal thymus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002691	small stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005046	absent spleen white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0005493	stomach epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0006173	abnormal myeloid dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20190613	MGI			
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IEA		N	RGD:5509061	20190613	MGI			
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20190613	MGI			
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008122	decreased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008167	increased B-1a cell number		IEA		N	RGD:5509061	20150702	MGI			
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008240	abnormal spleen marginal zone macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008343	abnormal gamma-delta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407039
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008471	abnormal spleen primary B follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008472	abnormal spleen secondary B follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008473	abnormal spleen follicular dendritic cell network		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008473	abnormal spleen follicular dendritic cell network		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008523	absent lymph node germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055593
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9359707
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0009322	increased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432976
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0009633	absent cervical lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18025196
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9432973
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391023
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0010798	abnormal stomach cardiac region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314550
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190613	MGI			
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015635
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20170223	MGI			PMID:20231695
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190613	MGI			
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0020416	decreased fibroblast chemotaxis		IAGP		N	RGD:5509061	20170223	MGI			PMID:20231695
1316231	Nfkb2	nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100	gene	MP:0030505	tooth impaction		IAGP		N	RGD:5509061	20191219	MGI			PMID:9359707
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342750
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342750
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342750
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342750
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342750
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342750
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22342750
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20160225	MGI			PMID:25896760
1316233	Pum1	pumilio RNA-binding family member 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:22342750
1316237	Usp16	ubiquitin specific peptidase 16	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1316237	Usp16	ubiquitin specific peptidase 16	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1316237	Usp16	ubiquitin specific peptidase 16	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1316237	Usp16	ubiquitin specific peptidase 16	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1316239	Myo10	myosin X	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20141120	MGI			
1316239	Myo10	myosin X	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1316239	Myo10	myosin X	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201231	MGI			
1316239	Myo10	myosin X	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20141003	MGI			
1316239	Myo10	myosin X	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20150108	MGI			
1316239	Myo10	myosin X	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20141003	MGI			
1316239	Myo10	myosin X	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20201231	MGI			
1316239	Myo10	myosin X	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0001413	abnormal response to new environment		IEA		N	RGD:5509061	20191128	MGI			
1316239	Myo10	myosin X	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170105	MGI			
1316239	Myo10	myosin X	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20141120	MGI			
1316239	Myo10	myosin X	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20170105	MGI			
1316239	Myo10	myosin X	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20201231	MGI			
1316239	Myo10	myosin X	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0005174	abnormal tail pigmentation		IEA		N	RGD:5509061	20141120	MGI			
1316239	Myo10	myosin X	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1316239	Myo10	myosin X	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20150108	MGI			
1316239	Myo10	myosin X	gene	MP:0008730	fused phalanges		IEA		N	RGD:5509061	20141003	MGI			
1316239	Myo10	myosin X	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0010714	iris coloboma		IEA		N	RGD:5509061	20141120	MGI			
1316239	Myo10	myosin X	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316239	Myo10	myosin X	gene	MP:0011277	decreased tail pigmentation		IEA		N	RGD:5509061	20141120	MGI			
1316239	Myo10	myosin X	gene	MP:0011877	absent liver		IAGP		N	RGD:5509061	20180301	MGI			PMID:29229982
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000262	poor arterial differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505817
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505817
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22529374
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0008823	abnormal interventricular septum membranous part morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0009163	absent pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:22529374
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22529374
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0009874	abnormal interdigital cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0010498	abnormal interventricular septum muscular part morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061358
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0012254	absent intersomitic vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:16000382
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0014554	delayed neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:18043734
1316243	Mib1	MIB E3 ubiquitin protein ligase 1	gene	MP:0031525	thin left ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:36325906
1316247	Zfp612	zinc finger protein 612	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316247	Zfp612	zinc finger protein 612	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1316247	Zfp612	zinc finger protein 612	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0001413	abnormal response to new environment		IEA		N	RGD:5509061	20141003	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466398
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466398
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20160421	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0002321	hypoventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466398
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0003578	absent ovary		IEA		N	RGD:5509061	20160811	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0005423	abnormal somatic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466398
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466398
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0021211	unilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0030190	small snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0031447	unilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:21982646
1316249	Pbx3	pre B cell leukemia homeobox 3	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:21982646
1316253	Ung	uracil DNA glycosylase	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934097
1316253	Ung	uracil DNA glycosylase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934097
1316253	Ung	uracil DNA glycosylase	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934097
1316253	Ung	uracil DNA glycosylase	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934097
1316253	Ung	uracil DNA glycosylase	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934097
1316253	Ung	uracil DNA glycosylase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1316253	Ung	uracil DNA glycosylase	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934097
1316253	Ung	uracil DNA glycosylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12934097
1316253	Ung	uracil DNA glycosylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1316253	Ung	uracil DNA glycosylase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10912000
1316253	Ung	uracil DNA glycosylase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12401169
1316253	Ung	uracil DNA glycosylase	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199406
1316253	Ung	uracil DNA glycosylase	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:19901081
1316253	Ung	uracil DNA glycosylase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12401169
1316253	Ung	uracil DNA glycosylase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20210722	MGI			PMID:31795137
1316253	Ung	uracil DNA glycosylase	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199406
1316253	Ung	uracil DNA glycosylase	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12401169
1316253	Ung	uracil DNA glycosylase	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1316253	Ung	uracil DNA glycosylase	gene	MP:0009796	abnormal base-excision repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1316253	Ung	uracil DNA glycosylase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1316253	Ung	uracil DNA glycosylase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1316253	Ung	uracil DNA glycosylase	gene	MP:0014762	impaired base-excision repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:22447450
1316253	Ung	uracil DNA glycosylase	gene	MP:0014766	impaired mismatch repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:22447450
1316256	Ubqlnl	ubiquilin-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1316256	Ubqlnl	ubiquilin-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26043068
1316259	Epha2	Eph receptor A2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287184
1316259	Epha2	Eph receptor A2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15054110
1316259	Epha2	Eph receptor A2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287184
1316259	Epha2	Eph receptor A2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287184
1316259	Epha2	Eph receptor A2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1316259	Epha2	Eph receptor A2	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849550
1316259	Epha2	Eph receptor A2	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20180215	MGI			PMID:28294115
1316259	Epha2	Eph receptor A2	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:19649315
1316259	Epha2	Eph receptor A2	gene	MP:0001684	abnormal axial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287184
1316259	Epha2	Eph receptor A2	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287184
1316259	Epha2	Eph receptor A2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287184
1316259	Epha2	Eph receptor A2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8649815
1316259	Epha2	Eph receptor A2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1316259	Epha2	Eph receptor A2	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287184
1316259	Epha2	Eph receptor A2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849550
1316259	Epha2	Eph receptor A2	gene	MP:0004713	split notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287184
1316259	Epha2	Eph receptor A2	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287184
1316259	Epha2	Eph receptor A2	gene	MP:0010255	cortical cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:19649315
1316259	Epha2	Eph receptor A2	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20180215	MGI			PMID:28294115
1316263	Ephx3	epoxide hydrolase 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180125	MGI			PMID:28384353
1316265	Lama1	laminin, alpha 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0001296	macrophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20170105	MGI			
1316265	Lama1	laminin, alpha 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1316265	Lama1	laminin, alpha 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1316265	Lama1	laminin, alpha 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15102706
1316265	Lama1	laminin, alpha 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15102706
1316265	Lama1	laminin, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100707
1316265	Lama1	laminin, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668394
1316265	Lama1	laminin, alpha 1	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1316265	Lama1	laminin, alpha 1	gene	MP:0003381	vitreal fibroplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668394
1316265	Lama1	laminin, alpha 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100707
1316265	Lama1	laminin, alpha 1	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100707
1316265	Lama1	laminin, alpha 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1316265	Lama1	laminin, alpha 1	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0009022	abnormal brain meninges morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0009026	abnormal brain pia mater morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0010235	abnormal retina inner limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0010387	abnormal Bergmann glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15102706
1316265	Lama1	laminin, alpha 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668394
1316265	Lama1	laminin, alpha 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100707
1316265	Lama1	laminin, alpha 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316265	Lama1	laminin, alpha 1	gene	MP:0011116	absent Reichert's membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:15102706
1316265	Lama1	laminin, alpha 1	gene	MP:0011116	absent Reichert's membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668394
1316265	Lama1	laminin, alpha 1	gene	MP:0011116	absent Reichert's membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100707
1316265	Lama1	laminin, alpha 1	gene	MP:0011116	absent Reichert's membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983115
1316265	Lama1	laminin, alpha 1	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100707
1316265	Lama1	laminin, alpha 1	gene	MP:0011187	abnormal parietal endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100707
1316265	Lama1	laminin, alpha 1	gene	MP:0012671	retina spots		IAGP		N	RGD:5509061	20141003	MGI			PMID:20048158
1316265	Lama1	laminin, alpha 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16100707
1316266	Bahcc1	BAH domain and coiled-coil containing 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1316266	Bahcc1	BAH domain and coiled-coil containing 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1316266	Bahcc1	BAH domain and coiled-coil containing 1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1316266	Bahcc1	BAH domain and coiled-coil containing 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20260402	MGI			
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20241121	MGI			
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20241121	MGI			
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23318132
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316269	Mei1	meiotic double-stranded break formation protein 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1316272	Rnf44	ring finger protein 44	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1316272	Rnf44	ring finger protein 44	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1316272	Rnf44	ring finger protein 44	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1316272	Rnf44	ring finger protein 44	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1316280	Adgrg7	adhesion G protein-coupled receptor G7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180308	MGI			PMID:24574718
1316280	Adgrg7	adhesion G protein-coupled receptor G7	gene	MP:0003291	interstinal hyperperistalsis		IAGP		N	RGD:5509061	20180308	MGI			PMID:24574718
1316280	Adgrg7	adhesion G protein-coupled receptor G7	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20211021	MGI			
1316280	Adgrg7	adhesion G protein-coupled receptor G7	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180308	MGI			PMID:24574718
1316280	Adgrg7	adhesion G protein-coupled receptor G7	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
1316280	Adgrg7	adhesion G protein-coupled receptor G7	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0004658	abnormal ventral tubercle of atlas morphology		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0005364	increased susceptibility to prion infection		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0009787	increased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0011919	abnormal R wave		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0013670	increased Ly6C-positive immature NK cell number		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316282	Pgap4	post-GPI attachment to proteins GalNAc transferase 4	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20231026	MGI			PMID:35151686
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20241121	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20200402	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20240613	MGI			PMID:35235343
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20200402	MGI			
1316289	Dyrk1b	dual-specificity tyrosine phosphorylation regulated kinase 1b	gene	MP:0012361	decreased large unstained cell number		IEA		N	RGD:5509061	20170105	MGI			
1316290	Fyb1	FYN binding protein 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567141
1316290	Fyb1	FYN binding protein 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20231207	MGI			
1316290	Fyb1	FYN binding protein 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
1316290	Fyb1	FYN binding protein 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646386
1316290	Fyb1	FYN binding protein 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567141
1316290	Fyb1	FYN binding protein 1	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567141
1316290	Fyb1	FYN binding protein 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20250508	MGI			
1316290	Fyb1	FYN binding protein 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567141
1316290	Fyb1	FYN binding protein 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646386
1316290	Fyb1	FYN binding protein 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567141
1316290	Fyb1	FYN binding protein 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646386
1316290	Fyb1	FYN binding protein 1	gene	MP:0010378	increased respiratory quotient		IEA		N	RGD:5509061	20231207	MGI			
1316291	Egfem1	EGF-like and EMI domain containing 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1316291	Egfem1	EGF-like and EMI domain containing 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1316291	Egfem1	EGF-like and EMI domain containing 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1316291	Egfem1	EGF-like and EMI domain containing 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1316291	Egfem1	EGF-like and EMI domain containing 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1316291	Egfem1	EGF-like and EMI domain containing 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1316291	Egfem1	EGF-like and EMI domain containing 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1316292	Tuba1c	tubulin, alpha 1C	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1316296	Raly	hnRNP-associated with lethal yellow	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20181227	MGI			
1316296	Raly	hnRNP-associated with lethal yellow	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1316296	Raly	hnRNP-associated with lethal yellow	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20181227	MGI			
1316296	Raly	hnRNP-associated with lethal yellow	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19168544
1316296	Raly	hnRNP-associated with lethal yellow	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
1316299	Moap1	modulator of apoptosis 1	gene	MP:0008891	decreased hepatocyte apoptosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:27320914
1316304	Aebp2	AE binding protein 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949878
1316304	Aebp2	AE binding protein 2	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949878
1316304	Aebp2	AE binding protein 2	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949878
1316304	Aebp2	AE binding protein 2	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949878
1316304	Aebp2	AE binding protein 2	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949878
1316304	Aebp2	AE binding protein 2	gene	MP:0005175	non-pigmented tail tip		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949878
1316304	Aebp2	AE binding protein 2	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949878
1316304	Aebp2	AE binding protein 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949878
1316307	Relch	RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1316307	Relch	RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1316307	Relch	RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1316307	Relch	RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1316307	Relch	RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1316307	Relch	RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1316307	Relch	RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1316307	Relch	RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0000543	absent urinary bladder urothelium		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20260402	MGI			
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0004006	impaired contractility of jejunal smooth muscle		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0009511	distended stomach		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0009854	impaired gastric peristalsis		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0011480	impaired ureteric peristalsis		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0011774	abnormal urinary bladder detrusor smooth muscle morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0013916	decreased intestine length		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316309	Lmod1	leiomodin 1 (smooth muscle)	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:28292896
1316311	Arhgap22	Rho GTPase activating protein 22	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1316311	Arhgap22	Rho GTPase activating protein 22	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1316311	Arhgap22	Rho GTPase activating protein 22	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20201022	MGI			
1316313	Nars1	asparaginyl-tRNA synthetase 1	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1316313	Nars1	asparaginyl-tRNA synthetase 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1316313	Nars1	asparaginyl-tRNA synthetase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:38495304
1316313	Nars1	asparaginyl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1316313	Nars1	asparaginyl-tRNA synthetase 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1316315	Dhx33	DEAH-box helicase 33	gene	MP:0005477	increased circulating thyroxine level		IEA		N	RGD:5509061	20211021	MGI			
1316315	Dhx33	DEAH-box helicase 33	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20210211	MGI			PMID:32767810
1316315	Dhx33	DEAH-box helicase 33	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316315	Dhx33	DEAH-box helicase 33	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316315	Dhx33	DEAH-box helicase 33	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:14576056
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:14576056
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170209	MGI			PMID:14576056
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:14744753
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:14576056
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14576056
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:14744753
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20170209	MGI			PMID:16476774
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:16476774
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14576056
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0008007	abnormal cellular replicative senescence		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0008007	abnormal cellular replicative senescence		IAGP		N	RGD:5509061	20170209	MGI			PMID:16476774
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009315	increased rectum adenocarcinoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20170209	MGI			PMID:14744753
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:14576056
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20170209	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:23878276
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20201224	MGI			PMID:31738183
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:14576056
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0020427	increased hepatocyte karyomegaly		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:15208629
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:23300461
1316317	Bub1b	BUB1B, mitotic checkpoint serine/threonine kinase	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:23878276
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430026
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430026
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430026
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430026
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430026
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430026
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0004680	small xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430026
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027331
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330926
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011200	abnormal extraembryonic coelom morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0012271	abnormal chordamesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017084
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0012282	abnormal sternebra number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430026
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0013505	decreased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17325035
1316320	Kat2a	K(lysine) acetyltransferase 2A	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:22002997
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15472465
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227763
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657845
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20250508	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200402	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210128	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15472465
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0008932	abnormal embryonic tissue physiology		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20240627	MGI			PMID:33246328
1316322	Zc3h4	zinc finger CCCH-type containing 4	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240627	MGI			
1316323	Slc25a44	solute carrier family 25, member 44	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210826	MGI			
1316323	Slc25a44	solute carrier family 25, member 44	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1316323	Slc25a44	solute carrier family 25, member 44	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20240307	MGI			PMID:33944778
1316323	Slc25a44	solute carrier family 25, member 44	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20240307	MGI			PMID:33944778
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15300255
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15300255
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15300255
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15300255
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15300255
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141003	MGI			
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15300255
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20220519	MGI			
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15300255
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485903
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15300255
1316327	Birc6	baculoviral IAP repeat-containing 6	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:15300255
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20230119	MGI			
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230119	MGI			
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230119	MGI			
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20230119	MGI			
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0008731	abnormal hair shaft melanin granule morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190207	MGI			PMID:26880576
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230119	MGI			
1316329	Rnaseh2a	ribonuclease H2, large subunit	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:26880576
1316333	Hoxc10	homeobox C10	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316333	Hoxc10	homeobox C10	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316333	Hoxc10	homeobox C10	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316333	Hoxc10	homeobox C10	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0003856	abnormal hindlimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0004614	caudal vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0004627	abnormal trochanter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0004654	absent lumbar vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0004694	absent patella		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1316333	Hoxc10	homeobox C10	gene	MP:0006429	abnormal hyaline cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0010240	decreased skeletal muscle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0030774	abnormal ischiofemoral ligament morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0030784	abnormal iliofemoral ligament morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:19623272
1316333	Hoxc10	homeobox C10	gene	MP:0030830	abnormal acetabulum morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:19623272
1316335	Pigb	phosphatidylinositol glycan anchor biosynthesis, class B	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20250508	MGI			
1316335	Pigb	phosphatidylinositol glycan anchor biosynthesis, class B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20180531	MGI			PMID:29082311
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20180531	MGI			PMID:29082311
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:29082311
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:29082311
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20180531	MGI			PMID:29082311
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:29082311
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0012203	abnormal neuronal stem cell morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:29082311
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0013220	increased pancreas apoptosis		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20180531	MGI			PMID:29082311
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20180607	MGI			PMID:24726366
1316337	Manf	mesencephalic astrocyte-derived neurotrophic factor	gene	MP:0020599	increased cerebral cortex cell density		IAGP		N	RGD:5509061	20180531	MGI			PMID:29082311
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0000328	increased enterocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0001235	disorganized suprabasal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0001329	retina hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0003269	colon polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041407
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20160811	MGI			PMID:26980762
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20160811	MGI			PMID:26980762
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20170223	MGI			PMID:26131558
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20160811	MGI			PMID:26980762
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041407
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041407
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20160811	MGI			PMID:26980762
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008109	abnormal small intestinal microvillus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041407
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0008992	abnormal portal lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0010040	abnormal oval cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0010040	abnormal oval cell morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26980762
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0010042	abnormal oval cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0010054	increased hepatoblastoma incidence		IAGP		N	RGD:5509061	20160811	MGI			PMID:26980762
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0010802	abnormal intestinal enteroendocrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0010945	lung epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160811	MGI			PMID:26980762
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369314
1316339	Sav1	salvador family WW domain containing 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404163
1316341	Gpalpp1	GPALPP motifs containing 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20230601	MGI			
1316341	Gpalpp1	GPALPP motifs containing 1	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1316341	Gpalpp1	GPALPP motifs containing 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20230601	MGI			
1316341	Gpalpp1	GPALPP motifs containing 1	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20241121	MGI			
1316343	Tbc1d31	TBC1 domain family, member 31	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1316343	Tbc1d31	TBC1 domain family, member 31	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0000829	dilated fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0000866	cerebellum vermis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0000923	abnormal roof plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1316347	Tmem67	transmembrane protein 67	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20160331	MGI			PMID:21725307
1316347	Tmem67	transmembrane protein 67	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1316347	Tmem67	transmembrane protein 67	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0003943	abnormal hepatobiliary system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20141003	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0004157	interrupted aortic arch		IEA		N	RGD:5509061	20141003	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0006100	abnormal tegmentum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0008282	enlarged hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20141003	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0009689	abnormal neural tube ventricular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0010422	heart right ventricle hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0010808	right-sided stomach		IEA		N	RGD:5509061	20141003	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1316347	Tmem67	transmembrane protein 67	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1316347	Tmem67	transmembrane protein 67	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1316347	Tmem67	transmembrane protein 67	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0011253	situs inversus with levocardia		IEA		N	RGD:5509061	20141003	MGI			
1316347	Tmem67	transmembrane protein 67	gene	MP:0011256	abnormal neural fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0012139	increased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0012259	meningocele		IAGP		N	RGD:5509061	20200910	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0012263	decreased hindbrain size		IAGP		N	RGD:5509061	20171109	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0014278	semilobar holoprosencephaly		IAGP		N	RGD:5509061	20230810	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0030309	abnormal posterior cranial fossa morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:23283079
1316347	Tmem67	transmembrane protein 67	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20230824	MGI			PMID:23283079
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0000372	irregular coat pigmentation		IEA		N	RGD:5509061	20150924	MGI			
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0000420	ruffled hair		IEA		N	RGD:5509061	20150924	MGI			
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0001290	delayed eyelid opening		IEA		N	RGD:5509061	20150924	MGI			
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20150924	MGI			
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0001511	disheveled coat		IEA		N	RGD:5509061	20150924	MGI			
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20150924	MGI			
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0002991	abnormal sebaceous gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0003136	yellow coat color		IEA		N	RGD:5509061	20150924	MGI			
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0005072	abnormal hair follicle melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0011019	abnormal adaptive thermogenesis		IAGP		N	RGD:5509061	20171228	MGI			PMID:14581464
1316353	Elovl3	ELOVL fatty acid elongase 3	gene	MP:0013146	eye lesions		IEA		N	RGD:5509061	20150924	MGI			
1316365	Lias	lipoic acid synthetase	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1316365	Lias	lipoic acid synthetase	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16135825
1316365	Lias	lipoic acid synthetase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16135825
1316365	Lias	lipoic acid synthetase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0004387	abnormal prechordal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16135825
1316365	Lias	lipoic acid synthetase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1316365	Lias	lipoic acid synthetase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1316365	Lias	lipoic acid synthetase	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1316365	Lias	lipoic acid synthetase	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20450902
1316365	Lias	lipoic acid synthetase	gene	MP:0012604	decreased glutathione level		IAGP		N	RGD:5509061	20180920	MGI			PMID:16135825
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20201022	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20210826	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20160804	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20210826	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0005573	increased pulmonary respiratory rate		IEA		N	RGD:5509061	20211021	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0010378	increased respiratory quotient		IEA		N	RGD:5509061	20210128	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316367	Epc2	enhancer of polycomb homolog 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20181115	MGI			PMID:24769727
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522767
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16162653
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:16162653
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857784
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127714
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127714
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522767
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522767
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16162653
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:24769727
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:24769727
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20181115	MGI			PMID:24769727
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522767
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0006342	absent first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522767
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0008732	reduced hair shaft melanin granule number		IAGP		N	RGD:5509061	20181115	MGI			PMID:24769727
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:24769727
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:24769727
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0009784	abnormal melanoblast migration		IAGP		N	RGD:5509061	20181115	MGI			PMID:24769727
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857784
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522767
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127714
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0012746	abnormal neural crest cell delamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522767
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522767
1316369	Zeb2	zinc finger E-box binding homeobox 2	gene	MP:0013011	absent vagal neural crest cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522767
1316371	Abcd4	ATP-binding cassette, sub-family D member 4	gene	MP:0001413	abnormal response to new environment		IEA		N	RGD:5509061	20141003	MGI			
1316371	Abcd4	ATP-binding cassette, sub-family D member 4	gene	MP:0005316	abnormal response to tactile stimuli		IEA		N	RGD:5509061	20141003	MGI			
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668895
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668895
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008644	increased circulating interleukin-12a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008647	increased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008666	increased interleukin-12a secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316378	Rps6ka4	ribosomal protein S6 kinase A4	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1316380	Timm21	translocase of inner mitochondrial membrane 21	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1316380	Timm21	translocase of inner mitochondrial membrane 21	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0000909	abnormal facial motor nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216204
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601927
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216204
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601927
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601927
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390667
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567614
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363146
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0004281	abnormal hypoglossal nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18216204
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601927
1316382	Nkx6-2	NK6 homeobox 2	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601927
1316384	Sacs	sacsin	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20181227	MGI			
1316384	Sacs	sacsin	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1316384	Sacs	sacsin	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20160128	MGI			PMID:22307627
1316384	Sacs	sacsin	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1316384	Sacs	sacsin	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1316384	Sacs	sacsin	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20190502	MGI			
1316384	Sacs	sacsin	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20181227	MGI			
1316384	Sacs	sacsin	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20160128	MGI			PMID:22307627
1316384	Sacs	sacsin	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:22307627
1316384	Sacs	sacsin	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0009426	decreased soleus weight		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160304	MGI			PMID:25260547
1316384	Sacs	sacsin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201022	MGI			
1316384	Sacs	sacsin	gene	MP:0014329	abnormal Purkinje cell axon morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:25260547
1316386	Brd4	bromodomain containing 4	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20190502	MGI			
1316386	Brd4	bromodomain containing 4	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20190502	MGI			
1316386	Brd4	bromodomain containing 4	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20191114	MGI			PMID:30830987
1316386	Brd4	bromodomain containing 4	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1316386	Brd4	bromodomain containing 4	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1316386	Brd4	bromodomain containing 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1316386	Brd4	bromodomain containing 4	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1316386	Brd4	bromodomain containing 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11997514
1316386	Brd4	bromodomain containing 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316386	Brd4	bromodomain containing 4	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1316386	Brd4	bromodomain containing 4	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1316386	Brd4	bromodomain containing 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316390	Rrp1	ribosomal RNA processing 1	gene	MP:0005534	decreased body temperature		IEA		N	RGD:5509061	20220519	MGI			
1316390	Rrp1	ribosomal RNA processing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316390	Rrp1	ribosomal RNA processing 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20251204	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505138
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:20603213
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0010059	olfactory bulb hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20603213
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881139
1316392	Sh2d3c	SH2 domain containing 3C	gene	MP:0014592	decreased gonadotropin-releasing hormone neuron number		IAGP		N	RGD:5509061	20241212	MGI			PMID:20881139
1316397	Gcat	glycine C-acetyltransferase (2-amino-3-ketobutyrate-coenzyme A ligase)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180503	MGI			PMID:29323231
1316401	Ebag9	estrogen receptor-binding fragment-associated gene 9	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620783
1316401	Ebag9	estrogen receptor-binding fragment-associated gene 9	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620783
1316401	Ebag9	estrogen receptor-binding fragment-associated gene 9	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620783
1316401	Ebag9	estrogen receptor-binding fragment-associated gene 9	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620783
1316403	Osbpl11	oxysterol binding protein-like 11	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20210520	MGI			
1316403	Osbpl11	oxysterol binding protein-like 11	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1316403	Osbpl11	oxysterol binding protein-like 11	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1316403	Osbpl11	oxysterol binding protein-like 11	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1316403	Osbpl11	oxysterol binding protein-like 11	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20260402	MGI			
1316403	Osbpl11	oxysterol binding protein-like 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0030758	increased circulating histamine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:15235600
1316405	Rabgef1	RAB guanine nucleotide exchange factor (GEF) 1	gene	MP:0031395	cutaneous mastocytosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:15235600
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0002649	abnormal enamel rod pattern		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0002772	brachypodia		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0003742	narrow head		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0004441	small occipital bone		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316406	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	gene	MP:0030245	round head		IAGP		N	RGD:5509061	20181011	MGI			PMID:30082715
1316410	Zic4	zinc finger protein of the cerebellum 4	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15338008
1316410	Zic4	zinc finger protein of the cerebellum 4	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15338008
1316410	Zic4	zinc finger protein of the cerebellum 4	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15338008
1316410	Zic4	zinc finger protein of the cerebellum 4	gene	MP:0000866	cerebellum vermis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15338008
1316410	Zic4	zinc finger protein of the cerebellum 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15338008
1316410	Zic4	zinc finger protein of the cerebellum 4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15338008
1316410	Zic4	zinc finger protein of the cerebellum 4	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15338008
1316410	Zic4	zinc finger protein of the cerebellum 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15338008
1316412	Wasf2	WASP family, member 2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20200514	MGI			
1316412	Wasf2	WASP family, member 2	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12853475
1316412	Wasf2	WASP family, member 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12853475
1316412	Wasf2	WASP family, member 2	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12853475
1316412	Wasf2	WASP family, member 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12853475
1316412	Wasf2	WASP family, member 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12853475
1316412	Wasf2	WASP family, member 2	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0003542	abnormal vascular endothelial cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20210128	MGI			
1316412	Wasf2	WASP family, member 2	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12853475
1316412	Wasf2	WASP family, member 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12853475
1316412	Wasf2	WASP family, member 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1316412	Wasf2	WASP family, member 2	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0012501	abnormal pericardial cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0020327	abnormal capillary branching pattern		IAGP		N	RGD:5509061	20160714	MGI			PMID:12879075
1316412	Wasf2	WASP family, member 2	gene	MP:0020329	decreased capillary density		IAGP		N	RGD:5509061	20160714	MGI			PMID:12879075
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000738	impaired muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20240516	MGI			PMID:30689883
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803290
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20240516	MGI			PMID:30689883
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20210422	MGI			PMID:30236258
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20220421	MGI			PMID:34257294
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210422	MGI			PMID:30236258
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803290
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139840
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23070698
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20210422	MGI			PMID:30236258
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20220421	MGI			PMID:34257294
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002318	hypercapnia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17122579
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003030	acidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17122579
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003030	acidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139840
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139840
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23070698
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139840
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004032	abnormal interventricular groove morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:32242214
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289290
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17122579
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20240516	MGI			PMID:30689883
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20240516	MGI			PMID:32242214
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004674	thin ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20181227	MGI			
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005247	abnormal extraocular muscle morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:32242214
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005369	muscle phenotype		IAGP		N	RGD:5509061	20240516	MGI			PMID:32242214
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005380	embryo phenotype		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005391	vision/eye phenotype		IAGP		N	RGD:5509061	20240516	MGI			PMID:32242214
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005573	increased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17122579
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289290
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803290
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9054435
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139840
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210422	MGI			PMID:30236258
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20220421	MGI			PMID:34257294
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009045	muscle tetany		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289290
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009046	muscle twitch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289290
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009411	abnormal skeletal muscle fiber triad morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:30689883
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009411	abnormal skeletal muscle fiber triad morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20240516	MGI			PMID:30689883
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210422	MGI			PMID:30236258
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17122579
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959667
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23070698
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0010405	ostium secundum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0011016	increased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139840
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7515481
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17122579
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20220421	MGI			PMID:34257294
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0011978	abnormal potassium ion homeostasis		IAGP		N	RGD:5509061	20160304	MGI			PMID:25564733
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0012514	pectus excavatum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284304
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:31044239
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0014918	decreased muscle cell calcium release		IAGP		N	RGD:5509061	20260219	MGI			PMID:18003898
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0020214	increased susceptibility to malignant hyperthermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17122579
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0020214	increased susceptibility to malignant hyperthermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139840
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0020214	increased susceptibility to malignant hyperthermia		IAGP		N	RGD:5509061	20210422	MGI			PMID:30236258
1316414	Ryr1	ryanodine receptor 1, skeletal muscle	gene	MP:0020214	increased susceptibility to malignant hyperthermia		IAGP		N	RGD:5509061	20220421	MGI			PMID:34257294
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082788
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0000958	peripheral nervous system degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082788
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082788
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20231207	MGI			
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303696
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082788
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1316420	Ndrg1	N-myc downstream regulated gene 1	gene	MP:0031204	hindlimb paresis		IAGP		N	RGD:5509061	20221110	MGI			PMID:35708320
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20190502	MGI			
1316425	Ndufa9	NADH:ubiquinone oxidoreductase subunit A9	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725297
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22340501
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0002421	abnormal cell-mediated immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12515813
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22340501
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12515813
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485735
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485735
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485735
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12515813
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12515813
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12515813
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12515813
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12515813
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485735
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485735
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485735
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714751
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485735
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0010160	increased oligodendrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725297
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0010205	abnormal oligodendrocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725297
1316427	Tnfrsf21	tumor necrosis factor receptor superfamily, member 21	gene	MP:0031384	impaired blood-brain barrier function		IAGP		N	RGD:5509061	20220407	MGI			PMID:22340501
1316434	Ppp4r2	protein phosphatase 4, regulatory subunit 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316434	Ppp4r2	protein phosphatase 4, regulatory subunit 2	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1316434	Ppp4r2	protein phosphatase 4, regulatory subunit 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20161201	MGI			
1316434	Ppp4r2	protein phosphatase 4, regulatory subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20180118	MGI			PMID:21228006
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505822
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000568	ectopic digits		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0001678	thick apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0002902	decreased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0002963	decreased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0003870	decreased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481602
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0004473	absent nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20260402	MGI			
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505822
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0010939	abnormal mandibular prominence morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17133501
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011471	decreased urine creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011496	abnormal head size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011843	abnormal kidney collecting duct epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0011858	elongated kidney papilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228006
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0012178	absent frontonasal prominence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0012182	abnormal presomitic mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0030324	abnormal anterior head development		IAGP		N	RGD:5509061	20171109	MGI			PMID:11702953
1316436	Dkk1	dickkopf WNT signaling pathway inhibitor 1	gene	MP:0030324	abnormal anterior head development		IAGP		N	RGD:5509061	20180118	MGI			PMID:17133501
1316439	Clba1	clathrin binding box of aftiphilin containing 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20201022	MGI			
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20180208	MGI			PMID:25074913
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0009598	thin epidermis stratum granulosum		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0011687	decreased epidermal stem cell number		IAGP		N	RGD:5509061	20180208	MGI			PMID:29078349
1316446	Slc39a10	solute carrier family 39 (zinc transporter), member 10	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20170615	MGI			PMID:27820601
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20170615	MGI			PMID:27820601
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20170615	MGI			PMID:27820601
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20170615	MGI			PMID:27820601
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20170615	MGI			PMID:27820601
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20170615	MGI			PMID:27820601
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20170615	MGI			PMID:27820601
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20170615	MGI			PMID:27820601
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:27820601
1316448	Scai	suppressor of cancer cell invasion	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:27820601
1316450	Adamts12	ADAM metallopeptidase with thrombospondin type 1 motif 12	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1316450	Adamts12	ADAM metallopeptidase with thrombospondin type 1 motif 12	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20210826	MGI			
1316450	Adamts12	ADAM metallopeptidase with thrombospondin type 1 motif 12	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
1316450	Adamts12	ADAM metallopeptidase with thrombospondin type 1 motif 12	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1316450	Adamts12	ADAM metallopeptidase with thrombospondin type 1 motif 12	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20208563
1316450	Adamts12	ADAM metallopeptidase with thrombospondin type 1 motif 12	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20208563
1316450	Adamts12	ADAM metallopeptidase with thrombospondin type 1 motif 12	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20208563
1316451	Katnip	katanin interacting protein	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20210128	MGI			
1316451	Katnip	katanin interacting protein	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20170504	MGI			PMID:26714646
1316451	Katnip	katanin interacting protein	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20170504	MGI			PMID:26714646
1316451	Katnip	katanin interacting protein	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
1316451	Katnip	katanin interacting protein	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1316451	Katnip	katanin interacting protein	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1316451	Katnip	katanin interacting protein	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20170504	MGI			PMID:26714646
1316451	Katnip	katanin interacting protein	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
1316451	Katnip	katanin interacting protein	gene	MP:0002958	cerebral aqueductal stenosis		IAGP		N	RGD:5509061	20170504	MGI			PMID:26714646
1316451	Katnip	katanin interacting protein	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210128	MGI			
1316451	Katnip	katanin interacting protein	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20170504	MGI			PMID:26714646
1316451	Katnip	katanin interacting protein	gene	MP:0013907	abnormal cerebrospinal fluid flow		IAGP		N	RGD:5509061	20170504	MGI			PMID:26714646
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0003950	abnormal plasma membrane morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316457	Pacsin3	protein kinase C and casein kinase substrate in neurons 3	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20250424	MGI			PMID:29202928
1316459	Trim7	tripartite motif-containing 7	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1316459	Trim7	tripartite motif-containing 7	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20201224	MGI			PMID:32126128
1316459	Trim7	tripartite motif-containing 7	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20201224	MGI			PMID:32126128
1316461	Gle1	GLE1 RNA export mediator	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1316461	Gle1	GLE1 RNA export mediator	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571074
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571074
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571074
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571074
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0000958	peripheral nervous system degeneration		IEA		N	RGD:5509061	20111116	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571074
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001391	abnormal tail movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20111215	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001393	ataxia		IEA		N	RGD:5509061	20190530	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20190530	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0001921	reduced fertility		IEA		N	RGD:5509061	20111116	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002752	abnormal somatic nervous system morphology		IEA		N	RGD:5509061	20111116	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0003492	abnormal involuntary movement		IEA		N	RGD:5509061	20111116	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0003633	abnormal nervous system physiology		IEA		N	RGD:5509061	20111116	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571074
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0004220	abnormal peripheral nervous system regeneration		IEA		N	RGD:5509061	20111116	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0004243	abnormal motor nerve collateral sprouting		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0004819	decreased skeletal muscle mass		IEA		N	RGD:5509061	20111116	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0005270	abnormal zygomatic bone morphology		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571074
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571074
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175812
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:7595654
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20180802	MGI			PMID:29437892
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0011954	shortened PQ interval		IEA		N	RGD:5509061	20260402	MGI			
1316463	Scyl1	SCY1-like 1 (S. cerevisiae)	gene	MP:0012000	abnormal limb position		IEA		N	RGD:5509061	20260402	MGI			
1316468	Abca8a	ATP-binding cassette, sub-family A member 8a	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20240523	MGI			
1316468	Abca8a	ATP-binding cassette, sub-family A member 8a	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20230601	MGI			
1316468	Abca8a	ATP-binding cassette, sub-family A member 8a	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20260402	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20260402	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0003543	abnormal vascular endothelial cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20260402	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20161229	MGI			PMID:27297885
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637190
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1316470	Pofut2	protein O-fucosyltransferase 2	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:20637190
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316475	Wdfy2	WD repeat and FYVE domain containing 2	gene	MP:0020102	increased hepatic glucose production		IAGP		N	RGD:5509061	20210513	MGI			PMID:32641353
1316477	Igdcc3	immunoglobulin superfamily, DCC subclass, member 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11486040
1316479	Trim33	tripartite motif-containing 33	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1316479	Trim33	tripartite motif-containing 33	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20220519	MGI			
1316479	Trim33	tripartite motif-containing 33	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1316479	Trim33	tripartite motif-containing 33	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
1316479	Trim33	tripartite motif-containing 33	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
1316479	Trim33	tripartite motif-containing 33	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543301
1316479	Trim33	tripartite motif-containing 33	gene	MP:0002583	absent extraembryonic ectoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
1316479	Trim33	tripartite motif-containing 33	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543301
1316479	Trim33	tripartite motif-containing 33	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0009110	pancreas hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
1316479	Trim33	tripartite motif-containing 33	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
1316479	Trim33	tripartite motif-containing 33	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
1316479	Trim33	tripartite motif-containing 33	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
1316479	Trim33	tripartite motif-containing 33	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629168
1316479	Trim33	tripartite motif-containing 33	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543301
1316479	Trim33	tripartite motif-containing 33	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1316479	Trim33	tripartite motif-containing 33	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0011197	abnormal proamniotic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0012159	absent anterior visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0012160	expanded anterior visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573697
1316479	Trim33	tripartite motif-containing 33	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20241121	MGI			
1316481	Ptpn4	protein tyrosine phosphatase, non-receptor type 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170209	MGI			PMID:17953619
1316481	Ptpn4	protein tyrosine phosphatase, non-receptor type 4	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20170209	MGI			PMID:17953619
1316481	Ptpn4	protein tyrosine phosphatase, non-receptor type 4	gene	MP:0002807	abnormal eye blink conditioning behavior		IAGP		N	RGD:5509061	20170209	MGI			PMID:17953619
1316483	Capn12	calpain 12	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1316483	Capn12	calpain 12	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1316483	Capn12	calpain 12	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1316483	Capn12	calpain 12	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1316483	Capn12	calpain 12	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1316483	Capn12	calpain 12	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1316483	Capn12	calpain 12	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1316483	Capn12	calpain 12	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1316485	Gpr137b	G protein-coupled receptor 137B	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1316486	Herpud2	HERPUD family member 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1316489	Zfp521	zinc finger protein 521	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21642473
1316489	Zfp521	zinc finger protein 521	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21173110
1316489	Zfp521	zinc finger protein 521	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:21642473
1316489	Zfp521	zinc finger protein 521	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21173110
1316489	Zfp521	zinc finger protein 521	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0008938	decreased pituitary gland weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0009393	abnormal resting posture		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21642473
1316489	Zfp521	zinc finger protein 521	gene	MP:0009911	increased hyoid bone size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21173110
1316489	Zfp521	zinc finger protein 521	gene	MP:0009912	decreased hyoid bone size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21173110
1316489	Zfp521	zinc finger protein 521	gene	MP:0009938	abnormal hippocampus granule cell morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20951345
1316489	Zfp521	zinc finger protein 521	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0012204	abnormal neuronal stem cell physiology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0013308	decreased adrenal gland weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24676388
1316489	Zfp521	zinc finger protein 521	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:24676388
1316491	Fbxo21	F-box protein 21	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20190502	MGI			
1316491	Fbxo21	F-box protein 21	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1316491	Fbxo21	F-box protein 21	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1316491	Fbxo21	F-box protein 21	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1316491	Fbxo21	F-box protein 21	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1316491	Fbxo21	F-box protein 21	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1316491	Fbxo21	F-box protein 21	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1316491	Fbxo21	F-box protein 21	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20221215	MGI			
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0009233	enlarged sperm head		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0009839	multiflagellated sperm		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0013538	increased Harderian gland adenoma incidence		IAGP		N	RGD:5509061	20150219	MGI			PMID:21124965
1316493	Ing2	inhibitor of growth family, member 2	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:21124965
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20220519	MGI			PMID:35258166
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20220519	MGI			PMID:35258166
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20220519	MGI			PMID:35258166
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20220519	MGI			PMID:35258166
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20220519	MGI			PMID:35258166
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20220519	MGI			PMID:35258166
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316495	Nhlrc2	NHL repeat containing 2	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20220519	MGI			PMID:35258166
1316496	Yju2	YJU2 splicing factor	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1316496	Yju2	YJU2 splicing factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316496	Yju2	YJU2 splicing factor	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316498	Glipr2	GLI pathogenesis-related 2	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20211216	MGI			PMID:33222586
1316499	Oasl2	2'-5' oligoadenylate synthetase-like 2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20210826	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20200514	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20200514	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20210826	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20210826	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20200514	MGI			
1316508	Tent4a	terminal nucleotidyltransferase 4A	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20200514	MGI			
1316509	Enkd1	enkurin domain containing 1	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0010393	shortened QRS complex duration		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0010748	abnormal visual evoked potential		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0011065	abnormal kidney epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0011919	abnormal R wave		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316509	Enkd1	enkurin domain containing 1	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:35301795
1316510	Lrrc10	leucine rich repeat containing 10	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20170803	MGI			PMID:23236519
1316510	Lrrc10	leucine rich repeat containing 10	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20170803	MGI			PMID:23236519
1316510	Lrrc10	leucine rich repeat containing 10	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20170803	MGI			PMID:23236519
1316510	Lrrc10	leucine rich repeat containing 10	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20170803	MGI			PMID:23236519
1316510	Lrrc10	leucine rich repeat containing 10	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20170803	MGI			PMID:23236519
1316510	Lrrc10	leucine rich repeat containing 10	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1316510	Lrrc10	leucine rich repeat containing 10	gene	MP:0015069	increased myocardial fiber length		IAGP		N	RGD:5509061	20260813	MGI			PMID:23236519
1316512	Brd9	bromodomain containing 9	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1316512	Brd9	bromodomain containing 9	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1316512	Brd9	bromodomain containing 9	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1316512	Brd9	bromodomain containing 9	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20210826	MGI			
1316512	Brd9	bromodomain containing 9	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20210826	MGI			
1316512	Brd9	bromodomain containing 9	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1316512	Brd9	bromodomain containing 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1316512	Brd9	bromodomain containing 9	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1316514	Atf1	activating transcription factor 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376811
1316514	Atf1	activating transcription factor 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0003695	delayed blastocyst hatching from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316514	Atf1	activating transcription factor 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11865068
1316515	Bcl2l12	BCL2 like 12	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20181227	MGI			
1316515	Bcl2l12	BCL2 like 12	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1316515	Bcl2l12	BCL2 like 12	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20181227	MGI			
1316515	Bcl2l12	BCL2 like 12	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1316515	Bcl2l12	BCL2 like 12	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1316515	Bcl2l12	BCL2 like 12	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0014045	Mallory bodies		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0014755	increased tumor cell proliferation		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316517	Bccip	BRCA2 and CDKN1A interacting protein	gene	MP:0031301	chronic liver inflammation		IAGP		N	RGD:5509061	20251009	MGI			PMID:32201259
1316521	Spata13	spermatogenesis associated 13	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:19893577
1316521	Spata13	spermatogenesis associated 13	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20190613	MGI			PMID:31020388
1316521	Spata13	spermatogenesis associated 13	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20190613	MGI			PMID:31020388
1316521	Spata13	spermatogenesis associated 13	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1316521	Spata13	spermatogenesis associated 13	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20190613	MGI			PMID:31020388
1316521	Spata13	spermatogenesis associated 13	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1316521	Spata13	spermatogenesis associated 13	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1316521	Spata13	spermatogenesis associated 13	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1316521	Spata13	spermatogenesis associated 13	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1316521	Spata13	spermatogenesis associated 13	gene	MP:0012434	decreased intestinal adenoma incidence		IAGP		N	RGD:5509061	20170413	MGI			PMID:19893577
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20221215	MGI			
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20220519	MGI			
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200514	MGI			
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0004203	abnormal cranial flexure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0004203	abnormal cranial flexure morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004860
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200514	MGI			
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0013208	abnormal cilium physiology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34211969
1316524	C2cd3	C2 calcium-dependent domain containing 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20190502	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20201022	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20201022	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1316526	Zbtb5	zinc finger and BTB domain containing 5	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1316529	Smyd4	SET and MYND domain containing 4	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1316529	Smyd4	SET and MYND domain containing 4	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1316529	Smyd4	SET and MYND domain containing 4	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1316531	Cdh5	cadherin 5	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857650
1316531	Cdh5	cadherin 5	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857650
1316531	Cdh5	cadherin 5	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0001619	abnormal vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857650
1316531	Cdh5	cadherin 5	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15855637
1316531	Cdh5	cadherin 5	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1316531	Cdh5	cadherin 5	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857650
1316531	Cdh5	cadherin 5	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22975327
1316531	Cdh5	cadherin 5	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:22025303
1316531	Cdh5	cadherin 5	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857650
1316531	Cdh5	cadherin 5	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0003230	abnormal umbilical artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0003390	lymphedema		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0003411	abnormal vein development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0003542	abnormal vascular endothelial cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0004832	enlarged ovary		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857650
1316531	Cdh5	cadherin 5	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1316531	Cdh5	cadherin 5	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1316531	Cdh5	cadherin 5	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22025303
1316531	Cdh5	cadherin 5	gene	MP:0009083	uterus hypertrophy		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0009251	enlarged endometrial glands		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1316531	Cdh5	cadherin 5	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857650
1316531	Cdh5	cadherin 5	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22025303
1316531	Cdh5	cadherin 5	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20151217	MGI			PMID:24487320
1316531	Cdh5	cadherin 5	gene	MP:0010195	abnormal lymphatic vessel endothelium morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0010197	abnormal lymphatic vessel endothelial cell morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857650
1316531	Cdh5	cadherin 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20151001	MGI			PMID:24567373
1316531	Cdh5	cadherin 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857650
1316531	Cdh5	cadherin 5	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10428027
1316531	Cdh5	cadherin 5	gene	MP:0012300	abnormal umbilical cord blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207135
1316531	Cdh5	cadherin 5	gene	MP:0013398	uterus fibrosis		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0013607	ovary fibrosis		IAGP		N	RGD:5509061	20160623	MGI			PMID:24858856
1316531	Cdh5	cadherin 5	gene	MP:0014400	increased hematopoietic precursor cell number		IAGP		N	RGD:5509061	20240321	MGI			PMID:24567373
1316537	Dnajb11	DnaJ heat shock protein family (Hsp40) member B11	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1316537	Dnajb11	DnaJ heat shock protein family (Hsp40) member B11	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20260402	MGI			
1316537	Dnajb11	DnaJ heat shock protein family (Hsp40) member B11	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1316537	Dnajb11	DnaJ heat shock protein family (Hsp40) member B11	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1316537	Dnajb11	DnaJ heat shock protein family (Hsp40) member B11	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1316537	Dnajb11	DnaJ heat shock protein family (Hsp40) member B11	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1316537	Dnajb11	DnaJ heat shock protein family (Hsp40) member B11	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1316537	Dnajb11	DnaJ heat shock protein family (Hsp40) member B11	gene	MP:0010574	dilated aorta		IEA		N	RGD:5509061	20211021	MGI			
1316537	Dnajb11	DnaJ heat shock protein family (Hsp40) member B11	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369260
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150813	MGI			PMID:26029872
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150813	MGI			PMID:26029872
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369260
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369260
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150813	MGI			PMID:26029872
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369260
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20150813	MGI			PMID:26029872
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20150813	MGI			PMID:26029872
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20150813	MGI			PMID:26029872
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20150813	MGI			PMID:26029872
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20150813	MGI			PMID:26029872
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369260
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20150813	MGI			PMID:26029872
1316540	Tarbp2	TARBP2, RISC loading complex RNA binding subunit	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:26029872
1316542	Rpa1	replication protein A1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1316542	Rpa1	replication protein A1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965476
1316542	Rpa1	replication protein A1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965476
1316542	Rpa1	replication protein A1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965476
1316542	Rpa1	replication protein A1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1316542	Rpa1	replication protein A1	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20211021	MGI			
1316542	Rpa1	replication protein A1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1316542	Rpa1	replication protein A1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1316542	Rpa1	replication protein A1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1316542	Rpa1	replication protein A1	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965476
1316542	Rpa1	replication protein A1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965476
1316542	Rpa1	replication protein A1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1316542	Rpa1	replication protein A1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965476
1316542	Rpa1	replication protein A1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316542	Rpa1	replication protein A1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965476
1316542	Rpa1	replication protein A1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316542	Rpa1	replication protein A1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1316543	Klc2	kinesin light chain 2	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20211021	MGI			
1316543	Klc2	kinesin light chain 2	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:34014435
1316543	Klc2	kinesin light chain 2	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:34014435
1316543	Klc2	kinesin light chain 2	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20240321	MGI			PMID:34014435
1316543	Klc2	kinesin light chain 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20240321	MGI			PMID:34014435
1316543	Klc2	kinesin light chain 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1316543	Klc2	kinesin light chain 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:34014435
1316543	Klc2	kinesin light chain 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20240321	MGI			PMID:34014435
1316543	Klc2	kinesin light chain 2	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20170105	MGI			
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20240523	MGI			
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0009131	decreased white fat cell number		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20240523	MGI			
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0014107	premature chondrocyte differentiation		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316545	Asap1	ArfGAP with SH3 domain, ankyrin repeat and PH domain1	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20190919	MGI			PMID:31246957
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20221201	MGI			PMID:34957483
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20221201	MGI			PMID:34957483
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20221201	MGI			PMID:34957483
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:27199445
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220811	MGI			
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20221201	MGI			PMID:34957483
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20221201	MGI			PMID:34957483
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20221201	MGI			PMID:34957483
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20180315	MGI			PMID:27199445
1316548	Jmjd8	jumonji domain containing 8	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20221201	MGI			PMID:34957483
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001220	epidermal necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354193
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001435	absent suckling reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001784	abnormal fluid regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354193
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354193
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0009602	abnormal keratohyalin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0009607	decreased keratohyalin granule size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20170921	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12697906
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23226340
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14512415
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0011159	abnormal epidermal-dermal junction morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0030572	abnormal pilosebaceous unit morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:12821645
1316552	Slc27a4	solute carrier family 27 (fatty acid transporter), member 4	gene	MP:0030798	joint contracture		IAGP		N	RGD:5509061	20181011	MGI			PMID:12821645
1316554	Il21	interleukin 21	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20231207	MGI			
1316554	Il21	interleukin 21	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581589
1316554	Il21	interleukin 21	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22466669
1316554	Il21	interleukin 21	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18602282
1316554	Il21	interleukin 21	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18602282
1316554	Il21	interleukin 21	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979605
1316554	Il21	interleukin 21	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18546146
1316554	Il21	interleukin 21	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581589
1316554	Il21	interleukin 21	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16979605
1316554	Il21	interleukin 21	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18602282
1316554	Il21	interleukin 21	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581589
1316554	Il21	interleukin 21	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18602282
1316554	Il21	interleukin 21	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18602282
1316554	Il21	interleukin 21	gene	MP:0008343	abnormal gamma-delta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581589
1316554	Il21	interleukin 21	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18602282
1316554	Il21	interleukin 21	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18602282
1316554	Il21	interleukin 21	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581589
1316556	Hcfc2	host cell factor C2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0002187	abnormal fibula morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0002419	abnormal innate immunity		IEA		N	RGD:5509061	20180125	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0003402	decreased liver weight		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20180125	MGI			PMID:28970238
1316556	Hcfc2	host cell factor C2	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20180125	MGI			PMID:28970238
1316556	Hcfc2	host cell factor C2	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20180125	MGI			PMID:28970238
1316556	Hcfc2	host cell factor C2	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20180125	MGI			PMID:28970238
1316556	Hcfc2	host cell factor C2	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0013520	increased CD4-positive NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0013523	increased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1316556	Hcfc2	host cell factor C2	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28970238
1316556	Hcfc2	host cell factor C2	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:28970238
1316556	Hcfc2	host cell factor C2	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:28970238
1316558	Gem	GTP binding protein overexpressed in skeletal muscle	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761801
1316558	Gem	GTP binding protein overexpressed in skeletal muscle	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761801
1316558	Gem	GTP binding protein overexpressed in skeletal muscle	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761801
1316558	Gem	GTP binding protein overexpressed in skeletal muscle	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761801
1316560	Nlrp10	NLR family, pyrin domain containing 10	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1316560	Nlrp10	NLR family, pyrin domain containing 10	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1316560	Nlrp10	NLR family, pyrin domain containing 10	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1316560	Nlrp10	NLR family, pyrin domain containing 10	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1316560	Nlrp10	NLR family, pyrin domain containing 10	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1316560	Nlrp10	NLR family, pyrin domain containing 10	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1316560	Nlrp10	NLR family, pyrin domain containing 10	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1316560	Nlrp10	NLR family, pyrin domain containing 10	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1316560	Nlrp10	NLR family, pyrin domain containing 10	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0004258	abnormal placenta size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0006372	impaired placental function		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316561	Rtl1	retrotransposon Gaglike 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176565
1316563	Mbd3	methyl-CpG binding domain protein 3	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196933
1316563	Mbd3	methyl-CpG binding domain protein 3	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196933
1316563	Mbd3	methyl-CpG binding domain protein 3	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196933
1316563	Mbd3	methyl-CpG binding domain protein 3	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21196933
1316563	Mbd3	methyl-CpG binding domain protein 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274056
1316563	Mbd3	methyl-CpG binding domain protein 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11274056
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3986619
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:423972
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055939
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20191212	MGI			PMID:30995482
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055939
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:423972
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3986619
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:423972
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:423972
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20191212	MGI			PMID:30995482
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004249	abnormal crista ampullaris morphology		IEA		N	RGD:5509061	20141003	MGI			
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004312	absent pillar cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:423972
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004328	decreased vestibular hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055939
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3986619
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004334	utricular macular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:3986619
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:423972
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8820880
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004396	decreased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055939
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004397	absent cochlear inner hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:423972
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8820880
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004518	absent vestibular hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055939
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004589	abnormal cochlear hair cell development		IEA		N	RGD:5509061	20210805	MGI			
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:16730938
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20191212	MGI			PMID:30995482
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0005307	head tossing		IEA		N	RGD:5509061	20210805	MGI			
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0006335	abnormal hearing electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4067076
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0006336	abnormal otoacoustic response		IAGP		N	RGD:5509061	20141003	MGI			PMID:4067076
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20191212	MGI			PMID:30995482
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16730938
1316565	Srrm4	serine/arginine repetitive matrix 4	gene	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm		IAGP		N	RGD:5509061	20161208	MGI			PMID:25838543
1316568	Wdr89	WD repeat domain 89	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210520	MGI			
1316571	Pnisr	PNN interacting serine/arginine-rich	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20241121	MGI			
1316571	Pnisr	PNN interacting serine/arginine-rich	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1316571	Pnisr	PNN interacting serine/arginine-rich	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1316571	Pnisr	PNN interacting serine/arginine-rich	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
1316571	Pnisr	PNN interacting serine/arginine-rich	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1316575	Mrps21	mitochondrial ribosomal protein S21	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0009119	increased brown fat cell size		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316579	Eepd1	endonuclease/exonuclease/phosphatase family domain containing 1	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20250605	MGI			PMID:39809799
1316580	Slc23a3	solute carrier family 23 (nucleobase transporters), member 3	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20181227	MGI			
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536716
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190808	MGI			
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410975
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536716
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395774
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160204	MGI			PMID:23955081
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536716
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0003582	abnormal ovary development		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004446	split exoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004710	small notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004713	split notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0006305	abnormal optic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20808772
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18536716
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20260813	MGI			PMID:12589020
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009015	short proestrus		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009018	short estrus		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009020	prolonged metestrus		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009233	enlarged sperm head		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926765
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0012180	abnormal somatic mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0012264	hindbrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0012424	decreased alimentary system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0012434	decreased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0012435	decreased colon tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955081
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0012659	decreased superoxide dismutase level		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0013482	abnormal duodenum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:18536716
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0013483	abnormal jejunum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:18536716
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0013662	decreased myeloid cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0013693	abnormal hemopoiesis		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0013892	increased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:22185780
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20220120	MGI			PMID:29559852
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0030834	acromion hypoplasia		IAGP		N	RGD:5509061	20181018	MGI			PMID:11290297
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0031018	decreased granulosa cell proliferation		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220120	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:30906217
1316582	Bmi1	Bmi1 proto-oncogene, polycomb ring finger	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:30906217
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018075
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018075
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0002658	abnormal liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0002698	abnormal sclera morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018075
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0003328	portal hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0003415	priapism		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20201001	MGI			PMID:11018075
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018075
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0005098	abnormal optic choroid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0005187	abnormal penis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0006137	venoocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11018075
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0020407	abnormal placental thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:14592998
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200924	MGI			PMID:11895779
1316584	Serpinc1	serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1	gene	MP:0031432	cornea perforation		IAGP		N	RGD:5509061	20220721	MGI			PMID:14592998
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130243
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130243
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230601	MGI			
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130243
1316587	Cxcl14	C-X-C motif chemokine ligand 14	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724031
1316589	Dazap2	DAZ associated protein 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1316589	Dazap2	DAZ associated protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10373015
1316589	Dazap2	DAZ associated protein 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20230119	MGI			
1316589	Dazap2	DAZ associated protein 2	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20230119	MGI			
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851594
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20181227	MGI			
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20181227	MGI			
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151210	MGI			PMID:22851594
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615127
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851594
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851594
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851594
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851594
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851594
1316590	Zbtb46	zinc finger and BTB domain containing 46	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316595	Ido2	indoleamine 2,3-dioxygenase 2	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20240215	MGI			PMID:34965962
1316595	Ido2	indoleamine 2,3-dioxygenase 2	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141030	MGI			PMID:24402311
1316595	Ido2	indoleamine 2,3-dioxygenase 2	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141030	MGI			PMID:24402311
1316595	Ido2	indoleamine 2,3-dioxygenase 2	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20240215	MGI			PMID:34965962
1316595	Ido2	indoleamine 2,3-dioxygenase 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141030	MGI			PMID:24402311
1316595	Ido2	indoleamine 2,3-dioxygenase 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141030	MGI			PMID:24402311
1316595	Ido2	indoleamine 2,3-dioxygenase 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141030	MGI			PMID:24402311
1316595	Ido2	indoleamine 2,3-dioxygenase 2	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141030	MGI			PMID:24402311
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20180920	MGI			PMID:26891723
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20190418	MGI			PMID:24403530
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20190418	MGI			PMID:24403530
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20180920	MGI			PMID:26891723
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20190418	MGI			PMID:24403530
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20180920	MGI			PMID:26891723
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20180920	MGI			PMID:26891723
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20180920	MGI			PMID:26891723
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20190418	MGI			PMID:24403530
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20180920	MGI			PMID:26891723
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20190418	MGI			PMID:24403530
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20180920	MGI			PMID:26891723
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:24403530
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:24403530
1316599	Dusp14	dual specificity phosphatase 14	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20180920	MGI			PMID:26891723
1316608	Plxnc1	plexin C1	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879062
1316608	Plxnc1	plexin C1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356169
1316608	Plxnc1	plexin C1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1316608	Plxnc1	plexin C1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356169
1316610	Foxi1	forkhead box I1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0000035	abnormal membranous labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0000525	renal tubular acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173882
1316610	Foxi1	forkhead box I1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932748
1316610	Foxi1	forkhead box I1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932748
1316610	Foxi1	forkhead box I1	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0003226	absent cochlear modiolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0004314	absent inner ear vestibule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0004316	enlarged vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0004335	enlarged utricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0004410	absent endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932748
1316610	Foxi1	forkhead box I1	gene	MP:0004922	abnormal common crus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0004928	increased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932748
1316610	Foxi1	forkhead box I1	gene	MP:0004931	enlarged epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932748
1316610	Foxi1	forkhead box I1	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0006014	dilated endolymphatic sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0006015	dilated lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0006016	dilated posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0006287	inner ear cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642503
1316610	Foxi1	forkhead box I1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932748
1316610	Foxi1	forkhead box I1	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173882
1316610	Foxi1	forkhead box I1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843211
1316610	Foxi1	forkhead box I1	gene	MP:0011843	abnormal kidney collecting duct epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173882
1316610	Foxi1	forkhead box I1	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220303	MGI			PMID:16932748
1316611	Fcamr	Fc receptor, IgA, IgM, high affinity	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549827
1316611	Fcamr	Fc receptor, IgA, IgM, high affinity	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549827
1316611	Fcamr	Fc receptor, IgA, IgM, high affinity	gene	MP:0008095	abnormal memory B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549827
1316611	Fcamr	Fc receptor, IgA, IgM, high affinity	gene	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549827
1316611	Fcamr	Fc receptor, IgA, IgM, high affinity	gene	MP:0008198	abnormal follicular dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549827
1316611	Fcamr	Fc receptor, IgA, IgM, high affinity	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549827
1316611	Fcamr	Fc receptor, IgA, IgM, high affinity	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549827
1316612	Tmem97	transmembrane protein 97	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20231207	MGI			
1316612	Tmem97	transmembrane protein 97	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20181227	MGI			
1316612	Tmem97	transmembrane protein 97	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20230601	MGI			
1316612	Tmem97	transmembrane protein 97	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20231207	MGI			
1316612	Tmem97	transmembrane protein 97	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1316612	Tmem97	transmembrane protein 97	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20201022	MGI			PMID:32588039
1316612	Tmem97	transmembrane protein 97	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0000282	abnormal interatrial septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20200402	MGI			
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150305	MGI			PMID:24646999
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20181227	MGI			
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20150305	MGI			PMID:24646999
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21825130
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0003898	abnormal QRS complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21825130
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0004116	abnormal atrioventricular bundle conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21825130
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20150305	MGI			PMID:24646999
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20150305	MGI			PMID:24646999
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20150305	MGI			PMID:24646999
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20150305	MGI			PMID:24646999
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20150305	MGI			PMID:24646999
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20150305	MGI			PMID:24646999
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21825130
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:21825130
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0011919	abnormal R wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:21825130
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1316614	Irx3	Iroquois related homeobox 3	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:24646999
1316616	Srsf7	serine and arginine-rich splicing factor 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211028	MGI			PMID:32146325
1316616	Srsf7	serine and arginine-rich splicing factor 7	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20211028	MGI			PMID:32146325
1316616	Srsf7	serine and arginine-rich splicing factor 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316616	Srsf7	serine and arginine-rich splicing factor 7	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:32146325
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0001836	abnormal antigen presentation via MHC class I		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0001841	decreased level of surface class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709825
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0002453	abnormal B lymphocyte antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0005046	absent spleen white pulp		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709825
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709825
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709825
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22197977
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008591	increased circulating interleukin-1 level		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316620	Psmb10	proteasome (prosome, macropain) subunit, beta type 10	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180524	MGI			PMID:29654304
1316623	Pcbp3	poly(rC) binding protein 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1316623	Pcbp3	poly(rC) binding protein 3	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1316623	Pcbp3	poly(rC) binding protein 3	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1316623	Pcbp3	poly(rC) binding protein 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1316630	Tbc1d2b	TBC1 domain family, member 2B	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1316630	Tbc1d2b	TBC1 domain family, member 2B	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160804	MGI			
1316630	Tbc1d2b	TBC1 domain family, member 2B	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20141003	MGI			
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0001806	decreased IgM level		IEA		N	RGD:5509061	20181011	MGI			
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572677
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572677
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17912374
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17912374
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572677
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572677
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572677
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17912374
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0008169	increased B-1b cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572677
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20181011	MGI			
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572677
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20181011	MGI			
1316635	Siglecg	sialic acid binding Ig-like lectin G	gene	MP:0010839	decreased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20181011	MGI			
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002414	abnormal myeloblast morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002445	abnormal mononuclear cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0003121	genetic imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0004692	small pubis		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0005573	increased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0008878	abnormal DNA methylation during gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1316637	Arid4a	AT-rich interaction domain 4A	gene	MP:0031070	hemophagocytosis		IAGP		N	RGD:5509061	20200618	MGI			PMID:18728284
1316638	D130043K22Rik	RIKEN cDNA D130043K22 gene	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20180208	MGI			PMID:27510895
1316638	D130043K22Rik	RIKEN cDNA D130043K22 gene	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1316638	D130043K22Rik	RIKEN cDNA D130043K22 gene	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20180208	MGI			PMID:27510895
1316639	Tmigd1	transmembrane and immunoglobulin domain containing 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:33129760
1316639	Tmigd1	transmembrane and immunoglobulin domain containing 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20210225	MGI			PMID:33129760
1316641	Trim6	tripartite motif-containing 6	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20220811	MGI			PMID:35533195
1316642	Nlrp5	NLR family, pyrin domain containing 5	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18804437
1316642	Nlrp5	NLR family, pyrin domain containing 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062459
1316642	Nlrp5	NLR family, pyrin domain containing 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18804437
1316642	Nlrp5	NLR family, pyrin domain containing 5	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1316642	Nlrp5	NLR family, pyrin domain containing 5	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062459
1316642	Nlrp5	NLR family, pyrin domain containing 5	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18804437
1316642	Nlrp5	NLR family, pyrin domain containing 5	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1316642	Nlrp5	NLR family, pyrin domain containing 5	gene	MP:0020850	abnormal microtubule cytoskeleton morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1316647	Gin1	gypsy retrotransposon integrase 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1316647	Gin1	gypsy retrotransposon integrase 1	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20210128	MGI			
1316647	Gin1	gypsy retrotransposon integrase 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1316647	Gin1	gypsy retrotransposon integrase 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20230601	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20260402	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220811	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220811	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220811	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220811	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220811	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17005861
1316653	Klhl1	kelch-like 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220811	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20220811	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20220519	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17005861
1316653	Klhl1	kelch-like 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17005861
1316653	Klhl1	kelch-like 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220811	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20220811	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20231207	MGI			
1316653	Klhl1	kelch-like 1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20220811	MGI			
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075356
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22661025
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22661025
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22661025
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075356
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22661025
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075356
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075356
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075356
1316658	Tiam1	T cell lymphoma invasion and metastasis 1	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20211021	MGI			
1316664	Smpdl3b	sphingomyelin phosphodiesterase, acid-like 3B	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20161124	MGI			PMID:26095358
1316664	Smpdl3b	sphingomyelin phosphodiesterase, acid-like 3B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20141003	MGI			
1316664	Smpdl3b	sphingomyelin phosphodiesterase, acid-like 3B	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:26095358
1316664	Smpdl3b	sphingomyelin phosphodiesterase, acid-like 3B	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20161124	MGI			PMID:26095358
1316664	Smpdl3b	sphingomyelin phosphodiesterase, acid-like 3B	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20161124	MGI			PMID:26095358
1316664	Smpdl3b	sphingomyelin phosphodiesterase, acid-like 3B	gene	MP:0008647	increased circulating interleukin-12b level		IAGP		N	RGD:5509061	20161124	MGI			PMID:26095358
1316664	Smpdl3b	sphingomyelin phosphodiesterase, acid-like 3B	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20161124	MGI			PMID:26095358
1316664	Smpdl3b	sphingomyelin phosphodiesterase, acid-like 3B	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20161124	MGI			PMID:26095358
1316664	Smpdl3b	sphingomyelin phosphodiesterase, acid-like 3B	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20161124	MGI			PMID:26095358
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20220519	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20111116	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8476712
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000644	dextrocardia		IEA		N	RGD:5509061	20111116	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1557392
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7723240
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8341011
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8476712
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0001924	infertility		IEA		N	RGD:5509061	20111116	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8476712
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666828
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666828
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20201022	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215348
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8341011
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8476712
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:7723240
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003266	biliary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003266	biliary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215348
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215348
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666828
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8476712
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:1557392
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22258617
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:7723240
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8341011
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8476712
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20111116	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8476712
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8341011
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8476712
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215348
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0008933	abnormal motile primary cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666828
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0008992	abnormal portal lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0008993	abnormal portal triad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:7723240
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0009342	enlarged gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:7723240
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0009343	dilated gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0009494	abnormal biliary ductule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0009500	abnormal interlobular bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666828
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1557392
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666828
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7723240
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11944981
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215348
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666828
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215348
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011252	situs inversus totalis		IEA		N	RGD:5509061	20111116	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215348
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:8887273
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0011665	d-loop transposition of the great arteries		IEA		N	RGD:5509061	20141003	MGI			
1316666	Bicc1	BicC family RNA binding protein 1	gene	MP:0012027	abnormal embryonic cilium location or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666828
1316670	Cldn17	claudin 17	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0003016	increased circulating bicarbonate level		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0003267	constipation		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0005634	decreased circulating sodium level		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316670	Cldn17	claudin 17	gene	MP:0012311	decreased defecation amount		IAGP		N	RGD:5509061	20220714	MGI			PMID:35681477
1316672	Krt14	keratin 14	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20241121	MGI			
1316672	Krt14	keratin 14	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792458
1316672	Krt14	keratin 14	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0000404	decreased curvature of zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371349
1316672	Krt14	keratin 14	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1316672	Krt14	keratin 14	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20241121	MGI			
1316672	Krt14	keratin 14	gene	MP:0000467	abnormal esophagus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539810
1316672	Krt14	keratin 14	gene	MP:0000648	absent sebaceous gland		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0001140	abnormal vagina epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539810
1316672	Krt14	keratin 14	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1316672	Krt14	keratin 14	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:11157990
1316672	Krt14	keratin 14	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1316672	Krt14	keratin 14	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539810
1316672	Krt14	keratin 14	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118961
1316672	Krt14	keratin 14	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792458
1316672	Krt14	keratin 14	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0001224	abnormal keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118961
1316672	Krt14	keratin 14	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539810
1316672	Krt14	keratin 14	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118961
1316672	Krt14	keratin 14	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20181220	MGI			PMID:22975380
1316672	Krt14	keratin 14	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20190124	MGI			PMID:28096290
1316672	Krt14	keratin 14	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1316672	Krt14	keratin 14	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1316672	Krt14	keratin 14	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118961
1316672	Krt14	keratin 14	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371349
1316672	Krt14	keratin 14	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539810
1316672	Krt14	keratin 14	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11157990
1316672	Krt14	keratin 14	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539810
1316672	Krt14	keratin 14	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1316672	Krt14	keratin 14	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:28096290
1316672	Krt14	keratin 14	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1316672	Krt14	keratin 14	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792458
1316672	Krt14	keratin 14	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20181220	MGI			PMID:22975380
1316672	Krt14	keratin 14	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20181220	MGI			PMID:22975380
1316672	Krt14	keratin 14	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20190124	MGI			PMID:28096290
1316672	Krt14	keratin 14	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241121	MGI			
1316672	Krt14	keratin 14	gene	MP:0004126	thin hypodermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23736260
1316672	Krt14	keratin 14	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20180913	MGI			PMID:24162662
1316672	Krt14	keratin 14	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:28096290
1316672	Krt14	keratin 14	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20181220	MGI			PMID:22975380
1316672	Krt14	keratin 14	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20190124	MGI			PMID:28096290
1316672	Krt14	keratin 14	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792458
1316672	Krt14	keratin 14	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20181220	MGI			PMID:22975380
1316672	Krt14	keratin 14	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1316672	Krt14	keratin 14	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0008538	decreased zigzag hair amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539810
1316672	Krt14	keratin 14	gene	MP:0009388	abnormal epidermal melanocyte morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:28096290
1316672	Krt14	keratin 14	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792458
1316672	Krt14	keratin 14	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20180913	MGI			PMID:24162662
1316672	Krt14	keratin 14	gene	MP:0009795	epidermal spongiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20181220	MGI			PMID:22975380
1316672	Krt14	keratin 14	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0010202	focal dorsal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635993
1316672	Krt14	keratin 14	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20180913	MGI			PMID:24162662
1316672	Krt14	keratin 14	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20181220	MGI			PMID:22975380
1316672	Krt14	keratin 14	gene	MP:0010318	increased salivary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23736260
1316672	Krt14	keratin 14	gene	MP:0011015	decreased body surface temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11157990
1316672	Krt14	keratin 14	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539810
1316672	Krt14	keratin 14	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316672	Krt14	keratin 14	gene	MP:0012022	increased melanocyte number		IAGP		N	RGD:5509061	20190124	MGI			PMID:28096290
1316672	Krt14	keratin 14	gene	MP:0012110	increased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23736260
1316672	Krt14	keratin 14	gene	MP:0012193	increased keratinocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792458
1316672	Krt14	keratin 14	gene	MP:0013374	increased sebaceous gland tumor incidence		IAGP		N	RGD:5509061	20180913	MGI			PMID:24162662
1316672	Krt14	keratin 14	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:23918954
1316672	Krt14	keratin 14	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23736260
1316672	Krt14	keratin 14	gene	MP:0014754	abnormal tumor progression		IAGP		N	RGD:5509061	20250925	MGI			PMID:23792458
1316672	Krt14	keratin 14	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:7539810
1316672	Krt14	keratin 14	gene	MP:0030529	abnormal head skin morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1316672	Krt14	keratin 14	gene	MP:0031395	cutaneous mastocytosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:23918954
1316674	Banp	BTG3 associated nuclear protein	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1316674	Banp	BTG3 associated nuclear protein	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210826	MGI			
1316674	Banp	BTG3 associated nuclear protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316674	Banp	BTG3 associated nuclear protein	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180503	MGI			PMID:29572490
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20180503	MGI			PMID:29572490
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20220519	MGI			
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180503	MGI			PMID:29572490
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20180503	MGI			PMID:29572490
1316676	Mgme1	mitochondrial genome maintenance exonuclease 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1316678	Cpne7	copine VII	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210128	MGI			
1316678	Cpne7	copine VII	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1316678	Cpne7	copine VII	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38105557
1316678	Cpne7	copine VII	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38105557
1316678	Cpne7	copine VII	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20240530	MGI			PMID:38105557
1316678	Cpne7	copine VII	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1316678	Cpne7	copine VII	gene	MP:0013250	abnormal dental pulp morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38105557
1316678	Cpne7	copine VII	gene	MP:0030453	abnormal odontoblast morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38105557
1316678	Cpne7	copine VII	gene	MP:0030559	abnormal dental pulp canal morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38105557
1316678	Cpne7	copine VII	gene	MP:0031626	increased dental pulp cell apoptosis		IAGP		N	RGD:5509061	20240620	MGI			PMID:38105557
1316680	Set	SET nuclear proto-oncogene	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20190912	MGI			PMID:30858352
1316680	Set	SET nuclear proto-oncogene	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20190912	MGI			PMID:30858352
1316680	Set	SET nuclear proto-oncogene	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:30858352
1316680	Set	SET nuclear proto-oncogene	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:30858352
1316680	Set	SET nuclear proto-oncogene	gene	MP:0012270	cardiac edema		IAGP		N	RGD:5509061	20190912	MGI			PMID:30858352
1316681	Rell1	RELT-like 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316681	Rell1	RELT-like 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1316681	Rell1	RELT-like 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1316681	Rell1	RELT-like 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220519	MGI			
1316683	Zfp276	zinc finger protein (C2H2 type) 276	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20240425	MGI			PMID:35137157
1316683	Zfp276	zinc finger protein (C2H2 type) 276	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1316683	Zfp276	zinc finger protein (C2H2 type) 276	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1316683	Zfp276	zinc finger protein (C2H2 type) 276	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20260402	MGI			
1316683	Zfp276	zinc finger protein (C2H2 type) 276	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20240425	MGI			PMID:35137157
1316683	Zfp276	zinc finger protein (C2H2 type) 276	gene	MP:0014318	abnormal oligodendrocyte differentiation		IAGP		N	RGD:5509061	20240425	MGI			PMID:35137157
1316683	Zfp276	zinc finger protein (C2H2 type) 276	gene	MP:0020868	decreased lipogenesis		IAGP		N	RGD:5509061	20240425	MGI			PMID:35137157
1316686	Cyp39a1	cytochrome P450, family 39, subfamily a, polypeptide 1	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20240523	MGI			
1316688	Pkp1	plakophilin 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0009598	thin epidermis stratum granulosum		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170601	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:27033150
1316688	Pkp1	plakophilin 1	gene	MP:0030605	abnormal corneocyte morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:27033150
1316689	Doc2g	double C2, gamma	gene	MP:0002915	abnormal synaptic depression		IAGP		N	RGD:5509061	20241031	MGI			PMID:33753311
1316689	Doc2g	double C2, gamma	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20241031	MGI			PMID:33753311
1316689	Doc2g	double C2, gamma	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20241031	MGI			PMID:33753311
1316689	Doc2g	double C2, gamma	gene	MP:0014253	decreased paired-pulse ratio		IAGP		N	RGD:5509061	20241031	MGI			PMID:33753311
1316700	Wdr3	WD repeat domain 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230406	MGI			PMID:36463953
1316700	Wdr3	WD repeat domain 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20230406	MGI			PMID:36463953
1316701	Ciao2a	cytosolic iron-sulfur assembly component 2A	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0003459	increased fear-related response		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20231207	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0008831	abnormal insulin-like growth factor I level		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0009455	enhanced cued conditioning behavior		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0009456	impaired cued conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0012318	slow extinction of fear memory		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0014115	cognitive inflexibility		IAGP		N	RGD:5509061	20190418	MGI			PMID:28867767
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20260813	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0020358	abnormal inhibitory synapse morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0020361	abnormal symmetric synapse morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20201022	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20210128	MGI			
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0020594	decreased cerebral cortex cell number		IAGP		N	RGD:5509061	20180621	MGI			PMID:28695822
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20250904	MGI			PMID:29184203
1316703	Arid1b	AT-rich interaction domain 1B	gene	MP:0030981	abnormal dentate gyrus subgranular zone morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:28695822
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20170518	MGI			PMID:24646517
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:24646517
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20160804	MGI			
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20170629	MGI			PMID:27939640
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0008262	abnormal hippocampus region morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:24646517
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:24646517
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:24646517
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0012203	abnormal neuronal stem cell morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:24646517
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0014744	abnormal hippocampal mossy fiber suprapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0020388	decreased radial glial cell number		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0020536	increased subiculum size		IAGP		N	RGD:5509061	20180301	MGI			PMID:25757017
1316706	Brpf1	bromodomain and PHD finger containing, 1	gene	MP:0030956	abnormal neuronal precursor cell migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:25757017
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0001037	abnormal parasympathetic neuron morphology		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0001945	bronchoconstriction		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0002337	abnormal whole-body plethysmography		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0006277	abnormal parasympathetic nervous system physiology		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0012593	increased brain choline acetyltransferase activity		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1316708	Cpeb2	cytoplasmic polyadenylation element binding protein 2	gene	MP:0030676	increased acetylcholine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:27810937
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0000226	abnormal mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0001588	abnormal hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0001589	abnormal mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316710	Hba-x	hemoglobin X, alpha-like embryonic chain in Hba complex	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242562
1316712	Cntrob	centrobin, centrosomal BRCA2 interacting protein	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20231207	MGI			
1316712	Cntrob	centrobin, centrosomal BRCA2 interacting protein	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20181227	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20210520	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210128	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20210128	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210520	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0009235	small sperm head		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1316713	AU040320	expressed sequence AU040320	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220224	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0020923	decreased susceptibility to Parvoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:26814968
1316713	AU040320	expressed sequence AU040320	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220303	MGI			PMID:29991750
1316713	AU040320	expressed sequence AU040320	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20220303	MGI			PMID:29991750
1316717	Rfx6	regulatory factor X, 6	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20148032
1316717	Rfx6	regulatory factor X, 6	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20148032
1316717	Rfx6	regulatory factor X, 6	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20148032
1316717	Rfx6	regulatory factor X, 6	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20148032
1316717	Rfx6	regulatory factor X, 6	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:20148032
1316717	Rfx6	regulatory factor X, 6	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1316717	Rfx6	regulatory factor X, 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240627	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160421	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20170629	MGI			PMID:26919979
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20170629	MGI			PMID:26919979
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20170629	MGI			PMID:26919979
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20170629	MGI			PMID:26919979
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0009567	mitotic nondisjunction		IAGP		N	RGD:5509061	20170629	MGI			PMID:26919979
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20170629	MGI			PMID:26919979
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20170629	MGI			PMID:26919979
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316719	Smc5	structural maintenance of chromosomes 5	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20170629	MGI			PMID:26919979
1316724	Arl5c	ADP-ribosylation factor-like 5C	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20221215	MGI			
1316724	Arl5c	ADP-ribosylation factor-like 5C	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20160811	MGI			
1316724	Arl5c	ADP-ribosylation factor-like 5C	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20160811	MGI			
1316724	Arl5c	ADP-ribosylation factor-like 5C	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1316724	Arl5c	ADP-ribosylation factor-like 5C	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20231207	MGI			
1316724	Arl5c	ADP-ribosylation factor-like 5C	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
1316728	Rad51	RAD51 recombinase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0002776	increased Sertoli cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692798
1316728	Rad51	RAD51 recombinase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0011191	increased embryonic epiblast cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0012142	absent amniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8943369
1316728	Rad51	RAD51 recombinase	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0014619	absent spermatogonia		IAGP		N	RGD:5509061	20250220	MGI			PMID:35292640
1316728	Rad51	RAD51 recombinase	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:35292640
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0000339	decreased enterocyte cell number		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001155	arrest of spermatogenesis		IEA		N	RGD:5509061	20141009	MGI			
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0002982	abnormal primordial germ cell migration		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0003578	absent ovary		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0004806	absent germ cells		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0004806	absent germ cells		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0004901	decreased male germ cell number		IEA		N	RGD:5509061	20141009	MGI			
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0005431	decreased oocyte number		IEA		N	RGD:5509061	20141009	MGI			
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0006428	ectopic Sertoli cells		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0008391	abnormal primordial germ cell morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0008393	absent primordial germ cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0008393	absent primordial germ cells		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141009	MGI			PMID:24356953
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0011610	abnormal primordial germ cell apoptosis		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20160526	MGI			PMID:24009519
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0030935	increased primordial germ cell apoptosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:23463509
1316730	Mad2l2	MAD2 mitotic arrest deficient-like 2	gene	MP:0030935	increased primordial germ cell apoptosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:24009519
1316731	Rnf214	ring finger protein 214	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1316731	Rnf214	ring finger protein 214	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316731	Rnf214	ring finger protein 214	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1316731	Rnf214	ring finger protein 214	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1316731	Rnf214	ring finger protein 214	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20220519	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20220519	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20210128	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240627	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20210128	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220519	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200402	MGI			
1316734	Ppfibp2	PTPRF interacting protein, binding protein 2 (liprin beta 2)	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20210527	MGI			PMID:33218264
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20220519	MGI			
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20241121	MGI			
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20210527	MGI			PMID:33218264
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0003043	hypoalgesia		IEA		N	RGD:5509061	20220519	MGI			
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20210527	MGI			PMID:33218264
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20210527	MGI			PMID:33218264
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20210527	MGI			PMID:33218264
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0020954	decreased mechanical nociceptive threshold		IEA		N	RGD:5509061	20220519	MGI			
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0020955	increased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20210527	MGI			PMID:33218264
1316736	Tecpr2	tectonin beta-propeller repeat containing 2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20210527	MGI			PMID:33218264
1316741	Gpx8	glutathione peroxidase 8 (putative)	gene	MP:0001194	dermatitis		IEA		N	RGD:5509061	20170406	MGI			
1316741	Gpx8	glutathione peroxidase 8 (putative)	gene	MP:0001222	epidermal hyperplasia		IEA		N	RGD:5509061	20170406	MGI			
1316741	Gpx8	glutathione peroxidase 8 (putative)	gene	MP:0001242	hyperkeratosis		IEA		N	RGD:5509061	20170406	MGI			
1316742	Mosmo	modulator of smoothened	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0000650	mesocardia		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0010854	lung situs inversus		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316742	Mosmo	modulator of smoothened	gene	MP:0031284	abdominal situs abnormality		IAGP		N	RGD:5509061	20211104	MGI			PMID:34486668
1316744	Pif1	PIF1 5'-to-3' DNA helicase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130244
1316744	Pif1	PIF1 5'-to-3' DNA helicase	gene	MP:0030928	increased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:17130244
1316752	Pmel	premelanosome protein	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949658
1316752	Pmel	premelanosome protein	gene	MP:0000372	irregular coat pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1316752	Pmel	premelanosome protein	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
1316752	Pmel	premelanosome protein	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949658
1316752	Pmel	premelanosome protein	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20210826	MGI			
1316752	Pmel	premelanosome protein	gene	MP:0008732	reduced hair shaft melanin granule number		IEA		N	RGD:5509061	20111116	MGI			
1316752	Pmel	premelanosome protein	gene	MP:0009933	abnormal tail hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949658
1316752	Pmel	premelanosome protein	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1316752	Pmel	premelanosome protein	gene	MP:0010192	abnormal retina melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949658
1316752	Pmel	premelanosome protein	gene	MP:0010193	abnormal choroid melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949658
1316755	Adam11	a disintegrin and metallopeptidase domain 11	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20210520	MGI			
1316755	Adam11	a disintegrin and metallopeptidase domain 11	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16504143
1316755	Adam11	a disintegrin and metallopeptidase domain 11	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16504143
1316756	Ccdc32	coiled-coil domain containing 32	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1316756	Ccdc32	coiled-coil domain containing 32	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1316756	Ccdc32	coiled-coil domain containing 32	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20260402	MGI			
1316756	Ccdc32	coiled-coil domain containing 32	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1316758	Sesn1	sestrin 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1316758	Sesn1	sestrin 1	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1316758	Sesn1	sestrin 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1316758	Sesn1	sestrin 1	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20181227	MGI			
1316758	Sesn1	sestrin 1	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1316758	Sesn1	sestrin 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316758	Sesn1	sestrin 1	gene	MP:0013762	abnormal effector T cell number		IAGP		N	RGD:5509061	20170810	MGI			PMID:28114291
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20210128	MGI			
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210826	MGI			
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1316762	Fam32a	family with sequence similarity 32, member A	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1316765	Klhl6	kelch-like 6	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1316765	Klhl6	kelch-like 6	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1316765	Klhl6	kelch-like 6	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1316765	Klhl6	kelch-like 6	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0003450	enlarged pancreas		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1316765	Klhl6	kelch-like 6	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20190411	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20181011	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1316765	Klhl6	kelch-like 6	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190110	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0008082	increased single-positive T cell number		IEA		N	RGD:5509061	20181011	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0008167	increased B-1a cell number		IEA		N	RGD:5509061	20190110	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20181011	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1316765	Klhl6	kelch-like 6	gene	MP:0008211	decreased mature B cell number		IEA		N	RGD:5509061	20141003	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0008214	increased immature B cell number		IEA		N	RGD:5509061	20141003	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1316765	Klhl6	kelch-like 6	gene	MP:0010842	decreased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20190110	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0013763	increased T-helper cell number		IEA		N	RGD:5509061	20240523	MGI			
1316765	Klhl6	kelch-like 6	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20240523	MGI			
1316767	Rnps1	RNA binding protein with serine rich domain 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20241121	MGI			
1316767	Rnps1	RNA binding protein with serine rich domain 1	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20241121	MGI			
1316767	Rnps1	RNA binding protein with serine rich domain 1	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20241121	MGI			
1316767	Rnps1	RNA binding protein with serine rich domain 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1316767	Rnps1	RNA binding protein with serine rich domain 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1316767	Rnps1	RNA binding protein with serine rich domain 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1316767	Rnps1	RNA binding protein with serine rich domain 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20241121	MGI			
1316767	Rnps1	RNA binding protein with serine rich domain 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1316769	Oxa1l	oxidase assembly 1-like	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20220811	MGI			
1316769	Oxa1l	oxidase assembly 1-like	gene	MP:0003043	hypoalgesia		IEA		N	RGD:5509061	20220519	MGI			
1316769	Oxa1l	oxidase assembly 1-like	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20220811	MGI			
1316769	Oxa1l	oxidase assembly 1-like	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316769	Oxa1l	oxidase assembly 1-like	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316769	Oxa1l	oxidase assembly 1-like	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21309068
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0009025	abnormal brain dura mater morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0010348	increased pancreatic islet cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655551
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21309068
1316775	Hic1	hypermethylated in cancer 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12539045
1316777	Kdm4c	lysine (K)-specific demethylase 4C	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20160804	MGI			
1316777	Kdm4c	lysine (K)-specific demethylase 4C	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1316777	Kdm4c	lysine (K)-specific demethylase 4C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161201	MGI			PMID:26248577
1316777	Kdm4c	lysine (K)-specific demethylase 4C	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20160804	MGI			
1316777	Kdm4c	lysine (K)-specific demethylase 4C	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20161201	MGI			PMID:26248577
1316777	Kdm4c	lysine (K)-specific demethylase 4C	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20160804	MGI			
1316777	Kdm4c	lysine (K)-specific demethylase 4C	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:24396064
1316777	Kdm4c	lysine (K)-specific demethylase 4C	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20161201	MGI			PMID:26248577
1316778	Fmn2	formin 2	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447394
1316778	Fmn2	formin 2	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447394
1316778	Fmn2	formin 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447394
1316778	Fmn2	formin 2	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447394
1316778	Fmn2	formin 2	gene	MP:0012737	abnormal primary polar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447394
1316778	Fmn2	formin 2	gene	MP:0014443	impaired polar body extrusion		IAGP		N	RGD:5509061	20240509	MGI			PMID:12447394
1316783	Ifngr2	interferon gamma receptor 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653170
1316783	Ifngr2	interferon gamma receptor 2	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714835
1316783	Ifngr2	interferon gamma receptor 2	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653170
1316783	Ifngr2	interferon gamma receptor 2	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714835
1316783	Ifngr2	interferon gamma receptor 2	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118001
1316783	Ifngr2	interferon gamma receptor 2	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653170
1316783	Ifngr2	interferon gamma receptor 2	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9653170
1316783	Ifngr2	interferon gamma receptor 2	gene	MP:0030960	abnormal diapedesis		IAGP		N	RGD:5509061	20190725	MGI			PMID:11714835
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15840700
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20230601	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382151
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382151
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522008
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9634821
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000757	herniated abdominal wall		IEA		N	RGD:5509061	20141003	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20230601	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001512	trunk curl		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15840700
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15840700
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423604
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566402
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20220519	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382151
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19856143
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729608
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003052	omphalocele		IEA		N	RGD:5509061	20141003	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003075	abnormal response to CNS ischemic injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147818
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382151
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152628
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152628
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20141003	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147818
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003924	diaphragmatic hernia		IEA		N	RGD:5509061	20141003	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003947	abnormal cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423604
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0004254	cerebral amyloid angiopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152628
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729608
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15840700
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038633
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038633
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739216
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15840700
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729608
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20201231	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147818
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147818
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0006134	artery occlusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0006265	increased pulse pressure		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0006278	aortic aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0008988	abnormal liver perisinusoidal space morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382151
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009137	decreased brown fat lipid droplet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522008
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729608
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729608
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729608
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010161	decreased brain cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010224	abnormal heart ventricle outflow tract morphology		IEA		N	RGD:5509061	20141003	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010332	abnormal circulating apolipoprotein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010333	abnormal circulating apolipoprotein E level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449704
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010470	dilated ascending aorta		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010659	abdominal aorta aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12690199
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011015	decreased body surface temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382151
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423604
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19856143
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382151
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011575	dilated aorta bulb		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011749	perivascular fibrosis		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20171228	MGI			PMID:24312398
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456862
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17948131
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0012329	increased circulating factor VIII level		IAGP		N	RGD:5509061	20201002	MGI			PMID:14739216
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0012329	increased circulating factor VIII level		IAGP		N	RGD:5509061	20201002	MGI			PMID:15840700
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0012329	increased circulating factor VIII level		IAGP		N	RGD:5509061	20201015	MGI			PMID:12522008
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0015055	decreased synapse density		IAGP		N	RGD:5509061	20260813	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20211014	MGI			PMID:21159977
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0031165	increased circulating von Willebrand factor level		IAGP		N	RGD:5509061	20201015	MGI			PMID:12522008
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0031165	increased circulating von Willebrand factor level		IAGP		N	RGD:5509061	20201015	MGI			PMID:14739216
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0031165	increased circulating von Willebrand factor level		IAGP		N	RGD:5509061	20201015	MGI			PMID:15840700
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0031510	increased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:12690199
1316787	Lrp1	low density lipoprotein receptor-related protein 1	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:17948131
1316789	Cse1l	chromosome segregation 1 like	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564884
1316789	Cse1l	chromosome segregation 1 like	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564884
1316789	Cse1l	chromosome segregation 1 like	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564884
1316790	Tex56	testis expressed 56	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240215	MGI			PMID:37938770
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0009263	abnormal eyelid fusion		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:37938770
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1316794	Tnrc18	trinucleotide repeat containing 18	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1316798	Fbxo33	F-box protein 33	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1316798	Fbxo33	F-box protein 33	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1316798	Fbxo33	F-box protein 33	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20170105	MGI			
1316802	Anxa13	annexin A13	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20260402	MGI			
1316802	Anxa13	annexin A13	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1316802	Anxa13	annexin A13	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20230601	MGI			
1316802	Anxa13	annexin A13	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1316802	Anxa13	annexin A13	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1316802	Anxa13	annexin A13	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20260402	MGI			
1316802	Anxa13	annexin A13	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0000263	absent organized vascular network		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925232
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0010241	abnormal aortic arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925232
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710940
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0014586	decreased egg cylinder size		IAGP		N	RGD:5509061	20241212	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:12588986
1316805	Paxip1	PAX interacting (with transcription-activation domain) protein 1	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:12588986
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20201022	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210128	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20190502	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20221215	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0020337	abnormal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0020512	abnormal dendritic mushroom spine morphology		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0021018	decreased dendritic spine number		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316807	Csmd3	CUB and Sushi multiple domains 3	gene	MP:0021090	abnormal dendrite arborization pattern		IAGP		N	RGD:5509061	20220421	MGI			PMID:35245678
1316809	Dctn6	dynactin 6	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20240801	MGI			
1316809	Dctn6	dynactin 6	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191205	MGI			
1316809	Dctn6	dynactin 6	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1316809	Dctn6	dynactin 6	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1316809	Dctn6	dynactin 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316809	Dctn6	dynactin 6	gene	MP:0011184	absent embryonic epiblast		IEA		N	RGD:5509061	20191205	MGI			
1316809	Dctn6	dynactin 6	gene	MP:0011185	absent primitive endoderm		IEA		N	RGD:5509061	20191205	MGI			
1316809	Dctn6	dynactin 6	gene	MP:0012102	absent trophectoderm		IEA		N	RGD:5509061	20191205	MGI			
1316809	Dctn6	dynactin 6	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316811	Sugt1	SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae)	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20221215	MGI			
1316811	Sugt1	SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316811	Sugt1	SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae)	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20151203	MGI			PMID:25985210
1316811	Sugt1	SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1316811	Sugt1	SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae)	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:25985210
1316814	Qsox2	quiescin Q6 sulfhydryl oxidase 2	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1316814	Qsox2	quiescin Q6 sulfhydryl oxidase 2	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20250508	MGI			
1316814	Qsox2	quiescin Q6 sulfhydryl oxidase 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1316816	Foxe3	forkhead box E3	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20170330	MGI			PMID:26854927
1316816	Foxe3	forkhead box E3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20201022	MGI			
1316816	Foxe3	forkhead box E3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20201022	MGI			
1316816	Foxe3	forkhead box E3	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20170209	MGI			PMID:10652278
1316816	Foxe3	forkhead box E3	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20170209	MGI			PMID:6373332
1316816	Foxe3	forkhead box E3	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210826	MGI			
1316816	Foxe3	forkhead box E3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20170209	MGI			PMID:11309658
1316816	Foxe3	forkhead box E3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11309658
1316816	Foxe3	forkhead box E3	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22002806
1316816	Foxe3	forkhead box E3	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6373332
1316816	Foxe3	forkhead box E3	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20170209	MGI			PMID:10652278
1316816	Foxe3	forkhead box E3	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20170209	MGI			PMID:11309658
1316816	Foxe3	forkhead box E3	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20170209	MGI			PMID:11980846
1316816	Foxe3	forkhead box E3	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20170209	MGI			PMID:10652278
1316816	Foxe3	forkhead box E3	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20170209	MGI			PMID:6373332
1316816	Foxe3	forkhead box E3	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20170209	MGI			PMID:10652278
1316816	Foxe3	forkhead box E3	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20170209	MGI			PMID:11980846
1316816	Foxe3	forkhead box E3	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11980846
1316816	Foxe3	forkhead box E3	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6373332
1316816	Foxe3	forkhead box E3	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20170209	MGI			PMID:11980846
1316816	Foxe3	forkhead box E3	gene	MP:0001320	small pupil		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0001320	small pupil		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1316816	Foxe3	forkhead box E3	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1316816	Foxe3	forkhead box E3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20201022	MGI			
1316816	Foxe3	forkhead box E3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20201022	MGI			
1316816	Foxe3	forkhead box E3	gene	MP:0002579	disorganized secondary lens fibers		IAGP		N	RGD:5509061	20170209	MGI			PMID:22002806
1316816	Foxe3	forkhead box E3	gene	MP:0002638	abnormal pupillary reflex		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10652278
1316816	Foxe3	forkhead box E3	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22002806
1316816	Foxe3	forkhead box E3	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:6373332
1316816	Foxe3	forkhead box E3	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10652278
1316816	Foxe3	forkhead box E3	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22002806
1316816	Foxe3	forkhead box E3	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20170330	MGI			PMID:26854927
1316816	Foxe3	forkhead box E3	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0004224	absent trabecular meshwork		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0004283	absent cornea endothelium		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20170330	MGI			PMID:26854927
1316816	Foxe3	forkhead box E3	gene	MP:0005099	abnormal ciliary body morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0005204	abnormal canal of Schlemm morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11980846
1316816	Foxe3	forkhead box E3	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20170209	MGI			PMID:22002806
1316816	Foxe3	forkhead box E3	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20170209	MGI			PMID:6373332
1316816	Foxe3	forkhead box E3	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20170330	MGI			PMID:26854927
1316816	Foxe3	forkhead box E3	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20170330	MGI			PMID:26854927
1316816	Foxe3	forkhead box E3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20170330	MGI			PMID:26854927
1316816	Foxe3	forkhead box E3	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20170330	MGI			PMID:26854927
1316816	Foxe3	forkhead box E3	gene	MP:0010255	cortical cataract		IAGP		N	RGD:5509061	20170209	MGI			PMID:22002806
1316816	Foxe3	forkhead box E3	gene	MP:0010259	anterior polar cataract		IAGP		N	RGD:5509061	20170209	MGI			PMID:22002806
1316816	Foxe3	forkhead box E3	gene	MP:0010470	dilated ascending aorta		IAGP		N	RGD:5509061	20170330	MGI			PMID:26854927
1316816	Foxe3	forkhead box E3	gene	MP:0010713	corneal-lenticular stalk		IAGP		N	RGD:5509061	20170209	MGI			PMID:11980846
1316816	Foxe3	forkhead box E3	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20170209	MGI			PMID:17064680
1316816	Foxe3	forkhead box E3	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20170209	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0014655	abnormal cornea curvature		IAGP		N	RGD:5509061	20250508	MGI			PMID:11980846
1316816	Foxe3	forkhead box E3	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:16199865
1316816	Foxe3	forkhead box E3	gene	MP:0031345	developmental cataract		IAGP		N	RGD:5509061	20220217	MGI			PMID:109409
1316816	Foxe3	forkhead box E3	gene	MP:0031345	developmental cataract		IAGP		N	RGD:5509061	20220217	MGI			PMID:6373332
1316820	Fech	ferrochelatase	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0001202	skin photosensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149233
1316820	Fech	ferrochelatase	gene	MP:0001202	skin photosensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0001202	skin photosensitivity		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18780836
1316820	Fech	ferrochelatase	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18780836
1316820	Fech	ferrochelatase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0004147	increased porphyrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0004147	increased porphyrin level		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0008387	hypochromic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0008991	abnormal bile canaliculus morphology		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0010175	leptocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149233
1316820	Fech	ferrochelatase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190808	MGI			PMID:28093505
1316820	Fech	ferrochelatase	gene	MP:0011188	increased erythrocyte protoporphyrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18780836
1316820	Fech	ferrochelatase	gene	MP:0011188	increased erythrocyte protoporphyrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1939658
1316820	Fech	ferrochelatase	gene	MP:0031084	decreased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:1939658
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0000716	abnormal immune system cell morphology		IEA		N	RGD:5509061	20111215	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0002444	abnormal T cell physiology		IEA		N	RGD:5509061	20111215	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20250508	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20221215	MGI			
1316822	Pstpip1	proline-serine-threonine phosphatase-interacting protein 1	gene	MP:0013763	increased T-helper cell number		IEA		N	RGD:5509061	20220811	MGI			
1316824	Rcc1l	reculator of chromosome condensation 1 like	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28746876
1316824	Rcc1l	reculator of chromosome condensation 1 like	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28746876
1316824	Rcc1l	reculator of chromosome condensation 1 like	gene	MP:0008495	decreased IgG1 level		IEA		N	RGD:5509061	20160804	MGI			
1316824	Rcc1l	reculator of chromosome condensation 1 like	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28746876
1316824	Rcc1l	reculator of chromosome condensation 1 like	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:28746876
1316825	Ranbp3l	RAN binding protein 3-like	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1316827	Med15	mediator complex subunit 15	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316827	Med15	mediator complex subunit 15	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316827	Med15	mediator complex subunit 15	gene	MP:0003926	decreased cellular glucose uptake		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316827	Med15	mediator complex subunit 15	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316827	Med15	mediator complex subunit 15	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316827	Med15	mediator complex subunit 15	gene	MP:0010147	abnormal endocrine pancreas physiology		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316827	Med15	mediator complex subunit 15	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316827	Med15	mediator complex subunit 15	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316827	Med15	mediator complex subunit 15	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316827	Med15	mediator complex subunit 15	gene	MP:0020423	abnormal mitochondrial biogenesis		IAGP		N	RGD:5509061	20250403	MGI			PMID:39379383
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20170413	MGI			PMID:25183008
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20170323	MGI			PMID:24356961
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20170323	MGI			PMID:24356961
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20170413	MGI			PMID:25183008
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20170413	MGI			PMID:25183008
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20170413	MGI			PMID:25183008
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170413	MGI			PMID:25183008
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20170323	MGI			PMID:24356961
1316834	Bloc1s1	biogenesis of lysosomal organelles complex-1, subunit 1	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20170323	MGI			PMID:24356961
1316840	Rac2	Rac family small GTPase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072071
1316840	Rac2	Rac family small GTPase 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072071
1316840	Rac2	Rac family small GTPase 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20201210	MGI			PMID:30723080
1316840	Rac2	Rac family small GTPase 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072071
1316840	Rac2	Rac family small GTPase 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20201210	MGI			PMID:30723080
1316840	Rac2	Rac family small GTPase 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072071
1316840	Rac2	Rac family small GTPase 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0001606	impaired hematopoiesis		IEA		N	RGD:5509061	20161201	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1316840	Rac2	Rac family small GTPase 2	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0001806	decreased IgM level		IEA		N	RGD:5509061	20150702	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11581314
1316840	Rac2	Rac family small GTPase 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072071
1316840	Rac2	Rac family small GTPase 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072071
1316840	Rac2	Rac family small GTPase 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12759446
1316840	Rac2	Rac family small GTPase 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18068132
1316840	Rac2	Rac family small GTPase 2	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0002494	increased IgM level		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18068132
1316840	Rac2	Rac family small GTPase 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20201210	MGI			PMID:30723080
1316840	Rac2	Rac family small GTPase 2	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20161201	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1316840	Rac2	Rac family small GTPase 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20201210	MGI			PMID:30723080
1316840	Rac2	Rac family small GTPase 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1316840	Rac2	Rac family small GTPase 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20201210	MGI			PMID:30723080
1316840	Rac2	Rac family small GTPase 2	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18068132
1316840	Rac2	Rac family small GTPase 2	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:30723080
1316840	Rac2	Rac family small GTPase 2	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0005078	abnormal cytotoxic T cell physiology		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11581314
1316840	Rac2	Rac family small GTPase 2	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18068132
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20201210	MGI			PMID:30723080
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20201210	MGI			PMID:30723080
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072071
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20160616	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20160616	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008600	decreased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11581314
1316840	Rac2	Rac family small GTPase 2	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072071
1316840	Rac2	Rac family small GTPase 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072071
1316840	Rac2	Rac family small GTPase 2	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0012765	decreased alpha-beta T cell number		IAGP		N	RGD:5509061	20201210	MGI			PMID:30723080
1316840	Rac2	Rac family small GTPase 2	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20180222	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20161201	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20150702	MGI			
1316840	Rac2	Rac family small GTPase 2	gene	MP:0020316	decreased vascular endothelial cell proliferation		IAGP		N	RGD:5509061	20160616	MGI			PMID:18068132
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591281
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271586
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271586
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15477599
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0010927	decreased osteoid volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732718
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271586
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393491
1316843	Ly6a	lymphocyte antigen 6 family member A	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:12732718
1316845	Bphl	biphenyl hydrolase like	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1316846	Tmem119	transmembrane protein 119	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20170105	MGI			
1316846	Tmem119	transmembrane protein 119	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20170105	MGI			
1316846	Tmem119	transmembrane protein 119	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20231026	MGI			PMID:37532932
1316846	Tmem119	transmembrane protein 119	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22416756
1316846	Tmem119	transmembrane protein 119	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20231026	MGI			PMID:37532932
1316848	Nat3	N-acetyltransferase 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403913
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0030966	decreased brain ependyma motile cilium number		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0031352	absent sperm axonemal central pair		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316852	Cfap70	cilia and flagella associated protein 70	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:37352829
1316853	Mapkbp1	mitogen-activated protein kinase binding protein 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1316853	Mapkbp1	mitogen-activated protein kinase binding protein 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1316853	Mapkbp1	mitogen-activated protein kinase binding protein 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20211021	MGI			
1316853	Mapkbp1	mitogen-activated protein kinase binding protein 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1316853	Mapkbp1	mitogen-activated protein kinase binding protein 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1316853	Mapkbp1	mitogen-activated protein kinase binding protein 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20160421	MGI			
1316855	Numbl	numb-like	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174898
1316855	Numbl	numb-like	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174898
1316855	Numbl	numb-like	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12410312
1316855	Numbl	numb-like	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174898
1316855	Numbl	numb-like	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12410312
1316855	Numbl	numb-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12410312
1316855	Numbl	numb-like	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0002653	abnormal ependyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174898
1316855	Numbl	numb-like	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174898
1316855	Numbl	numb-like	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12410312
1316855	Numbl	numb-like	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174898
1316855	Numbl	numb-like	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174898
1316855	Numbl	numb-like	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12410312
1316855	Numbl	numb-like	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174898
1316855	Numbl	numb-like	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12410312
1316855	Numbl	numb-like	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0011724	ectopic cortical neuron		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1316855	Numbl	numb-like	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12410312
1316855	Numbl	numb-like	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:14687546
1316857	Fbxo4	F-box protein 4	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22124152
1316857	Fbxo4	F-box protein 4	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0009222	increased uterus tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0009439	increased myeloid sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316857	Fbxo4	F-box protein 4	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21911473
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160237
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20201022	MGI			
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20200514	MGI			
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160237
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20201022	MGI			
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160237
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210128	MGI			
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160237
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0008581	disorganized photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20161222	MGI			PMID:26216965
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0011059	abnormal ependyma motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0011281	abnormal olfactory epithelium cilium morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:15322545
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:18032602
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20160218	MGI			PMID:23160237
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20161117	MGI			PMID:23160237
1316859	Bbs1	Bardet-Biedl syndrome 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20191128	MGI			PMID:31479441
1316862	Hoxc5	homeobox C5	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316862	Hoxc5	homeobox C5	gene	MP:0012668	absent sternal manubrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1316864	Efhd2	EF hand domain containing 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20160225	MGI			PMID:25092375
1316864	Efhd2	EF hand domain containing 2	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20160225	MGI			PMID:25092375
1316864	Efhd2	EF hand domain containing 2	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20160225	MGI			PMID:25133820
1316864	Efhd2	EF hand domain containing 2	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20160225	MGI			PMID:25092375
1316864	Efhd2	EF hand domain containing 2	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25092375
1316864	Efhd2	EF hand domain containing 2	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25092375
1316864	Efhd2	EF hand domain containing 2	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20160225	MGI			PMID:25092375
1316864	Efhd2	EF hand domain containing 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20160225	MGI			PMID:25092375
1316864	Efhd2	EF hand domain containing 2	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20160225	MGI			PMID:25092375
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892084
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774718
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20160421	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896504
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896504
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20150827	MGI			PMID:19896504
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896504
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896504
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774718
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892084
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892084
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896504
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20160421	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896504
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896504
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0003842	abnormal metopic suture morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774718
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160421	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20170105	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20181227	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009121	increased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009137	decreased brown fat lipid droplet number		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175442
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892084
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0010614	abnormal mitral valve cusp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892084
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0010625	absent tricuspid valve cusps		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892084
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23892084
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774718
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1316869	Ehmt1	euchromatic histone methyltransferase 1	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20180118	MGI			PMID:26376866
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20180118	MGI			PMID:26376866
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20190502	MGI			
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180118	MGI			PMID:26376866
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0003631	nervous system phenotype		IAGP		N	RGD:5509061	20260813	MGI			PMID:34686877
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20180118	MGI			PMID:26376866
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0009980	abnormal cerebellum dentate nucleus morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:26376866
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180118	MGI			PMID:26376866
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180118	MGI			PMID:26376866
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20180118	MGI			PMID:26376866
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0011877	absent liver		IAGP		N	RGD:5509061	20180118	MGI			PMID:26376866
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1316871	Thap1	THAP domain containing, apoptosis associated protein 1	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20260813	MGI			PMID:34686877
1316873	Flii	flightless I actin binding protein	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190808	MGI			
1316873	Flii	flightless I actin binding protein	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971982
1316873	Flii	flightless I actin binding protein	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1316873	Flii	flightless I actin binding protein	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326236
1316873	Flii	flightless I actin binding protein	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1316873	Flii	flightless I actin binding protein	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971982
1316873	Flii	flightless I actin binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316873	Flii	flightless I actin binding protein	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1316877	Lin28a	lin-28 homolog A	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1316877	Lin28a	lin-28 homolog A	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962509
1316877	Lin28a	lin-28 homolog A	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962509
1316877	Lin28a	lin-28 homolog A	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20512147
1316877	Lin28a	lin-28 homolog A	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20512147
1316877	Lin28a	lin-28 homolog A	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316877	Lin28a	lin-28 homolog A	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23378032
1316877	Lin28a	lin-28 homolog A	gene	MP:0012681	collapsed brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1316885	Arel1	apoptosis resistant E3 ubiquitin protein ligase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316885	Arel1	apoptosis resistant E3 ubiquitin protein ligase 1	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31578312
1316885	Arel1	apoptosis resistant E3 ubiquitin protein ligase 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1316885	Arel1	apoptosis resistant E3 ubiquitin protein ligase 1	gene	MP:0020001	decreased response to antigen		IAGP		N	RGD:5509061	20200402	MGI			PMID:31578312
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23115618
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20200402	MGI			
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23115618
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23115618
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23115618
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23115618
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0003858	enhanced coordination		IEA		N	RGD:5509061	20141003	MGI			
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20211021	MGI			
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23115618
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0005180	abnormal circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23115618
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23115618
1316890	Ifitm1	interferon induced transmembrane protein 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1316899	Hexb	hexosaminidase B	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
1316899	Hexb	hexosaminidase B	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
1316899	Hexb	hexosaminidase B	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
1316899	Hexb	hexosaminidase B	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1316899	Hexb	hexosaminidase B	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12617783
1316899	Hexb	hexosaminidase B	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
1316899	Hexb	hexosaminidase B	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550345
1316899	Hexb	hexosaminidase B	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550345
1316899	Hexb	hexosaminidase B	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
1316899	Hexb	hexosaminidase B	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1316899	Hexb	hexosaminidase B	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20210304	MGI			PMID:31547903
1316899	Hexb	hexosaminidase B	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
1316899	Hexb	hexosaminidase B	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
1316899	Hexb	hexosaminidase B	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
1316899	Hexb	hexosaminidase B	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
1316899	Hexb	hexosaminidase B	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
1316899	Hexb	hexosaminidase B	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20181227	MGI			
1316899	Hexb	hexosaminidase B	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
1316899	Hexb	hexosaminidase B	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550345
1316899	Hexb	hexosaminidase B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550345
1316899	Hexb	hexosaminidase B	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1316899	Hexb	hexosaminidase B	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
1316899	Hexb	hexosaminidase B	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
1316899	Hexb	hexosaminidase B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550345
1316899	Hexb	hexosaminidase B	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
1316899	Hexb	hexosaminidase B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
1316899	Hexb	hexosaminidase B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
1316899	Hexb	hexosaminidase B	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20210304	MGI			PMID:31547903
1316899	Hexb	hexosaminidase B	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12617783
1316899	Hexb	hexosaminidase B	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9645704
1316899	Hexb	hexosaminidase B	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20210304	MGI			PMID:31547903
1316899	Hexb	hexosaminidase B	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550345
1316899	Hexb	hexosaminidase B	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12617783
1316899	Hexb	hexosaminidase B	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9645704
1316899	Hexb	hexosaminidase B	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
1316899	Hexb	hexosaminidase B	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550345
1316899	Hexb	hexosaminidase B	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1316899	Hexb	hexosaminidase B	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
1316899	Hexb	hexosaminidase B	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9184660
1316899	Hexb	hexosaminidase B	gene	MP:0003807	camptodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0004100	abnormal spinal cord interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0004143	muscle hypertonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0004676	wide ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0004728	abnormal efferent ductules of testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9645704
1316899	Hexb	hexosaminidase B	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7550345
1316899	Hexb	hexosaminidase B	gene	MP:0004928	increased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9645704
1316899	Hexb	hexosaminidase B	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31547903
1316899	Hexb	hexosaminidase B	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789434
1316899	Hexb	hexosaminidase B	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20181227	MGI			
1316899	Hexb	hexosaminidase B	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20210128	MGI			
1316899	Hexb	hexosaminidase B	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
1316899	Hexb	hexosaminidase B	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155903
1316899	Hexb	hexosaminidase B	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1316899	Hexb	hexosaminidase B	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028353
1316899	Hexb	hexosaminidase B	gene	MP:0009249	enlarged caput epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9645704
1316899	Hexb	hexosaminidase B	gene	MP:0009256	enlarged corpus epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9645704
1316899	Hexb	hexosaminidase B	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021458
1316899	Hexb	hexosaminidase B	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20181227	MGI			
1316899	Hexb	hexosaminidase B	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:14722612
1316899	Hexb	hexosaminidase B	gene	MP:0020851	abnormal vacuole morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31547903
1316899	Hexb	hexosaminidase B	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:8896570
1316899	Hexb	hexosaminidase B	gene	MP:0030262	frontal bossing		IAGP		N	RGD:5509061	20171026	MGI			PMID:8896570
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20210520	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20220811	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20201022	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210826	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20201022	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20201022	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0004155	decreased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20201022	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316900	Ube2f	ubiquitin-conjugating enzyme E2F (putative)	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20220519	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20210826	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20200514	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220519	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20220519	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20220519	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0008548	abnormal circulating interferon level		IAGP		N	RGD:5509061	20190117	MGI			PMID:25008915
1316902	Trim13	tripartite motif-containing 13	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20190117	MGI			PMID:25008915
1316902	Trim13	tripartite motif-containing 13	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20190117	MGI			PMID:25008915
1316902	Trim13	tripartite motif-containing 13	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1316902	Trim13	tripartite motif-containing 13	gene	MP:0031039	decreased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:25008915
1316903	Raver2	ribonucleoprotein, PTB-binding 2	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1316903	Raver2	ribonucleoprotein, PTB-binding 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425408
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425408
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425408
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425408
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425408
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22549958
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700192
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425408
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23318132
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425408
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425408
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:37612290
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425408
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660953
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660954
1316905	Dmc1	DNA meiotic recombinase 1	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478856
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000478	delayed intestine development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20210218	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001889	delayed brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0005141	liver hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442273
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17643102
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0010952	abnormal fatty acid beta-oxidation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442273
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288097
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0011634	abnormal mitochondrial inner membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:15732085
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:17442273
1316907	Pex5	peroxisomal biogenesis factor 5	gene	MP:0031204	hindlimb paresis		IAGP		N	RGD:5509061	20210218	MGI			PMID:17643102
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20180111	MGI			PMID:25980009
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20180111	MGI			PMID:25980009
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20180111	MGI			PMID:25980009
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20180111	MGI			PMID:25980009
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210520	MGI			
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20180111	MGI			PMID:25980009
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180111	MGI			PMID:25980009
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0013648	increased CD11b-high dendritic cell number		IAGP		N	RGD:5509061	20180111	MGI			PMID:25980009
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0014026	abnormal respiratory epithelial transmembrane transport		IAGP		N	RGD:5509061	20180111	MGI			PMID:25980009
1316909	Stard7	StAR related lipid transfer domain containing 7	gene	MP:0014032	abnormal mucous gland morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:25980009
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191128	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191128	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0003886	abnormal embryonic epiblast morphology		IEA		N	RGD:5509061	20191128	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191128	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20181220	MGI			PMID:25581363
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191128	MGI			
1316911	Ube2m	ubiquitin-conjugating enzyme E2M	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20170105	MGI			
1316913	Rabl6	RAB, member RAS oncogene family-like 6	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1316913	Rabl6	RAB, member RAS oncogene family-like 6	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1316913	Rabl6	RAB, member RAS oncogene family-like 6	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1316915	Yars1	tyrosyl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1316915	Yars1	tyrosyl-tRNA synthetase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
1316915	Yars1	tyrosyl-tRNA synthetase 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20231207	MGI			
1316915	Yars1	tyrosyl-tRNA synthetase 1	gene	MP:0020845	abnormal DNA-templated transcription		IAGP		N	RGD:5509061	20220407	MGI			PMID:34516839
1316917	Adsl	adenylosuccinate lyase	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20190502	MGI			
1316917	Adsl	adenylosuccinate lyase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1316917	Adsl	adenylosuccinate lyase	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20161201	MGI			
1316917	Adsl	adenylosuccinate lyase	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1316917	Adsl	adenylosuccinate lyase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316917	Adsl	adenylosuccinate lyase	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20210722	MGI			PMID:33942714
1316917	Adsl	adenylosuccinate lyase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000071	axial skeleton hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20812917
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20812917
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148564
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:20812917
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20812917
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20812917
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20141003	MGI			
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148564
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148564
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:20812917
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20812917
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148564
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148564
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20812917
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148564
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148564
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0008910	thin long bone epiphysis		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148564
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0009897	decreased maxillary shelf size		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0011650	abnormal cornea stroma collagen fibril morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0030132	periodontium inflammation		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0030178	abnormal scalp morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0030198	nasal septum hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0030245	round head		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0030445	abnormal sphenooccipital synchondrosis		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0030584	skin atrophy		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0030797	joint laxity		IAGP		N	RGD:5509061	20221006	MGI			PMID:30459452
1316918	Csgalnact1	chondroitin sulfate N-acetylgalactosaminyltransferase 1	gene	MP:0031450	nasal cartilage hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:30459452
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000561	adactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20150305	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003315	abnormal perineum morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004383	absent interparietal bone		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004419	absent parietal bone		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004653	absent caudal vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004656	absent sacral vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004870	small premaxilla		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0009053	abnormal anal canal morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0009947	abnormal olfactory bulb external plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0009950	abnormal olfactory bulb internal plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470284
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0011771	abnormal genital tubercle morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0011772	genital tubercle hypoplasia		IAGP		N	RGD:5509061	20151112	MGI			PMID:23358455
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14526104
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0012761	increased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0013164	abnormal forelimb bud morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:14597661
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0013199	increased head mesenchyme apoptosis		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0030190	small snout		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316920	Sp8	trans-acting transcription factor 8	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1316922	Catsper2	cation channel, sperm associated 2	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:14657366
1316922	Catsper2	cation channel, sperm associated 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14657366
1316922	Catsper2	cation channel, sperm associated 2	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1316922	Catsper2	cation channel, sperm associated 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14657366
1316922	Catsper2	cation channel, sperm associated 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1316922	Catsper2	cation channel, sperm associated 2	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1316922	Catsper2	cation channel, sperm associated 2	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:14657366
1316926	Rhoh	ras homolog family member H	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1316926	Rhoh	ras homolog family member H	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17028588
1316926	Rhoh	ras homolog family member H	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17028588
1316926	Rhoh	ras homolog family member H	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19124738
1316926	Rhoh	ras homolog family member H	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17028588
1316926	Rhoh	ras homolog family member H	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17028588
1316926	Rhoh	ras homolog family member H	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19124738
1316926	Rhoh	ras homolog family member H	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316926	Rhoh	ras homolog family member H	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19124738
1316926	Rhoh	ras homolog family member H	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119112
1316928	Borcs5	BLOC-1 related complex subunit 5	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:32553155
1316928	Borcs5	BLOC-1 related complex subunit 5	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1316928	Borcs5	BLOC-1 related complex subunit 5	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:32553155
1316928	Borcs5	BLOC-1 related complex subunit 5	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:32553155
1316928	Borcs5	BLOC-1 related complex subunit 5	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20210401	MGI			PMID:32553155
1316928	Borcs5	BLOC-1 related complex subunit 5	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210401	MGI			PMID:32553155
1316928	Borcs5	BLOC-1 related complex subunit 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122227
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20151224	MGI			PMID:23122227
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24405768
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24405768
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20151224	MGI			PMID:23122227
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0008850	increased hemoglobin concentration distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0008850	increased hemoglobin concentration distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122227
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0008954	abnormal cellular hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24405768
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:24405768
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0010511	shortened PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0010738	abnormal internode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0010738	abnormal internode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24405768
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0011730	increased myelin sheath thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0011730	increased myelin sheath thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:24405768
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:24405768
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0011913	abnormal reticulocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122227
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0011954	shortened PQ interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:19544475
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0012365	increased erythrocyte sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122227
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0012367	decreased erythrocyte magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122227
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0012370	decreased erythrocyte potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122227
1316930	Kel	Kell metallo-endopeptidase	gene	MP:0012372	abnormal erythrocyte ion content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23122227
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20160428	MGI			PMID:23452852
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20260813	MGI			PMID:42310454
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0001148	enlarged testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23967333
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729857
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729857
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23103168
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20160428	MGI			PMID:23452852
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729857
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23967333
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20160428	MGI			PMID:23452852
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0003154	abnormal soft palate morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729857
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23967333
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20729857
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0009896	palatine bone horizontal plate hypoplasia		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0010745	abnormal pre-Botzinger complex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23103168
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0010746	abnormal pre-Botzinger complex physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23103168
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23103168
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23103168
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0012174	flat head		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0013475	delayed reproductive senescence		IAGP		N	RGD:5509061	20220616	MGI			PMID:23967333
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0014106	delayed chondrocyte differentiation		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:23103168
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160929	MGI			PMID:25587042
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0021216	abnormal palatal mesenchymal cell differentiation		IAGP		N	RGD:5509061	20230302	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0030224	abnormal soft palate muscle morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1316935	Kdm6b	KDM1 lysine (K)-specific demethylase 6B	gene	MP:0031425	enhanced male fertility		IAGP		N	RGD:5509061	20220714	MGI			PMID:23967333
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20260402	MGI			
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20260402	MGI			
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1316941	Chaf1b	chromatin assembly factor 1, subunit B	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0010134	decreased DN3 thymocyte number		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316945	Zbtb35	zinc finger and BTB domain containing 35	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20211021	MGI			PMID:26136427
1316948	Arsj	arylsulfatase J	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210826	MGI			
1316948	Arsj	arylsulfatase J	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1316948	Arsj	arylsulfatase J	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1316948	Arsj	arylsulfatase J	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210826	MGI			
1316948	Arsj	arylsulfatase J	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1316948	Arsj	arylsulfatase J	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210826	MGI			
1316948	Arsj	arylsulfatase J	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20220519	MGI			
1316958	Lpin1	lipin 1	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0000424	retarded hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:2722772
1316958	Lpin1	lipin 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559480
1316958	Lpin1	lipin 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559480
1316958	Lpin1	lipin 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0000958	peripheral nervous system degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0001105	abnormal PNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559480
1316958	Lpin1	lipin 1	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559480
1316958	Lpin1	lipin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559480
1316958	Lpin1	lipin 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2722772
1316958	Lpin1	lipin 1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:2722772
1316958	Lpin1	lipin 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1316958	Lpin1	lipin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130489
1316958	Lpin1	lipin 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559480
1316958	Lpin1	lipin 1	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559480
1316958	Lpin1	lipin 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1316958	Lpin1	lipin 1	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130489
1316958	Lpin1	lipin 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669885
1316958	Lpin1	lipin 1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1316958	Lpin1	lipin 1	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130489
1316958	Lpin1	lipin 1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130489
1316958	Lpin1	lipin 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130489
1316958	Lpin1	lipin 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130489
1316958	Lpin1	lipin 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559480
1316958	Lpin1	lipin 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0005440	increased glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130489
1316958	Lpin1	lipin 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130489
1316958	Lpin1	lipin 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397848
1316958	Lpin1	lipin 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:2722772
1316958	Lpin1	lipin 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18559480
1316958	Lpin1	lipin 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0008976	delayed female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0009122	decreased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669885
1316958	Lpin1	lipin 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0010052	increased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2722772
1316958	Lpin1	lipin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160128	MGI			PMID:22908270
1316958	Lpin1	lipin 1	gene	MP:0011579	decreased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:2050689
1316958	Lpin1	lipin 1	gene	MP:0011591	decreased hormone-sensitive lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:10884287
1316958	Lpin1	lipin 1	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:11138012
1316958	Lpin1	lipin 1	gene	MP:0014958	decreased lung enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0014966	decreased heart enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0014970	decreased muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0014972	decreased spleen enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0014975	decreased kidney enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1316958	Lpin1	lipin 1	gene	MP:0030863	decreased joint mobility		IAGP		N	RGD:5509061	20181101	MGI			PMID:19793967
1316958	Lpin1	lipin 1	gene	MP:0031203	forelimb paresis		IAGP		N	RGD:5509061	20210218	MGI			PMID:19793967
1316960	Sytl2	synaptotagmin-like 2	gene	MP:0000505	decreased digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16716193
1316960	Sytl2	synaptotagmin-like 2	gene	MP:0004137	abnormal gastric surface mucous cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16716193
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0002236	abnormal internal nares morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0010752	impaired mucociliary clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0010752	impaired mucociliary clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1316961	Dpcd	deleted in primary ciliary dyskinesia	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080492
1316963	Wdr6	WD repeat domain 6	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1316963	Wdr6	WD repeat domain 6	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20220811	MGI			
1316963	Wdr6	WD repeat domain 6	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20220811	MGI			
1316963	Wdr6	WD repeat domain 6	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20231207	MGI			
1316963	Wdr6	WD repeat domain 6	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20240523	MGI			
1316963	Wdr6	WD repeat domain 6	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1316965	Mrps17	mitochondrial ribosomal protein S17	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20260402	MGI			
1316967	Cblc	Cbl proto-oncogene c	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14560016
1316968	Psg16	pregnancy specific beta-1-glycoprotein 16	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20250508	MGI			
1316968	Psg16	pregnancy specific beta-1-glycoprotein 16	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1316970	Ap1m1	adaptor-related protein complex AP-1, mu subunit 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811610
1316970	Ap1m1	adaptor-related protein complex AP-1, mu subunit 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811610
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20260402	MGI			
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21737674
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316972	Rit1	Ras-like without CAAX 1	gene	MP:0030245	round head		IAGP		N	RGD:5509061	20190905	MGI			PMID:30898653
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20181227	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20170105	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0010378	increased respiratory quotient		IEA		N	RGD:5509061	20210128	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20250508	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0011939	increased food intake		IEA		N	RGD:5509061	20211021	MGI			
1316975	Dppa1	developmental pluripotency associated 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20250508	MGI			
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20250508	MGI			
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20250508	MGI			
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1316982	Tbc1d7	TBC1 domain family, member 7	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20220630	MGI			PMID:35584673
1316984	Ankrd9	ankyrin repeat domain 9	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20201022	MGI			
1316984	Ankrd9	ankyrin repeat domain 9	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1316984	Ankrd9	ankyrin repeat domain 9	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1316984	Ankrd9	ankyrin repeat domain 9	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20150430	MGI			
1316984	Ankrd9	ankyrin repeat domain 9	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20150430	MGI			
1316984	Ankrd9	ankyrin repeat domain 9	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20150430	MGI			
1316986	Peg12	paternally expressed 12	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15681612
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858271
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858271
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858271
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0008830	abnormal nucleolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858271
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858271
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858271
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160818	MGI			PMID:25708872
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1316987	Emg1	EMG1 N1-specific pseudouridine methyltransferase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1316993	Myoz2	myozenin 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987565
1316993	Myoz2	myozenin 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987565
1316993	Myoz2	myozenin 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987565
1316993	Myoz2	myozenin 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987565
1316993	Myoz2	myozenin 2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987565
1316993	Myoz2	myozenin 2	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987565
1316993	Myoz2	myozenin 2	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987565
1316993	Myoz2	myozenin 2	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:15543153
1316993	Myoz2	myozenin 2	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987565
1316996	Med23	mediator complex subunit 23	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0000128	growth retardation of molars		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19417216
1316996	Med23	mediator complex subunit 23	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:21305688
1316996	Med23	mediator complex subunit 23	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1316996	Med23	mediator complex subunit 23	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:21305688
1316996	Med23	mediator complex subunit 23	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210128	MGI			PMID:21305688
1316996	Med23	mediator complex subunit 23	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1316996	Med23	mediator complex subunit 23	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1316996	Med23	mediator complex subunit 23	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19417216
1316996	Med23	mediator complex subunit 23	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20210128	MGI			PMID:21305688
1316996	Med23	mediator complex subunit 23	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1316996	Med23	mediator complex subunit 23	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19417216
1316996	Med23	mediator complex subunit 23	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0004476	absent palatine bone		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1316996	Med23	mediator complex subunit 23	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1316996	Med23	mediator complex subunit 23	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972934
1316996	Med23	mediator complex subunit 23	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20210128	MGI			PMID:21305688
1316996	Med23	mediator complex subunit 23	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210520	MGI			
1316996	Med23	mediator complex subunit 23	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
1316996	Med23	mediator complex subunit 23	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1316996	Med23	mediator complex subunit 23	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19417216
1316996	Med23	mediator complex subunit 23	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:21305688
1316996	Med23	mediator complex subunit 23	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1316996	Med23	mediator complex subunit 23	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1316996	Med23	mediator complex subunit 23	gene	MP:0012756	impaired cranial neural crest cell differentiation		IAGP		N	RGD:5509061	20210128	MGI			PMID:21305688
1316996	Med23	mediator complex subunit 23	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0013268	second pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20210128	MGI			PMID:21305688
1316996	Med23	mediator complex subunit 23	gene	MP:0014012	abnormal cranial blood vasculature morphology		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0020326	dilated capillary		IAGP		N	RGD:5509061	20260416	MGI			PMID:35440711
1316996	Med23	mediator complex subunit 23	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0030080	small lower incisors		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0030170	absent mandibular symphysis		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0030249	small frontonasal prominence		IAGP		N	RGD:5509061	20210128	MGI			PMID:21305688
1316996	Med23	mediator complex subunit 23	gene	MP:0030259	mandibular condyloid process hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0030374	Meckel's cartilage hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0030467	abnormal cranial cartilage development		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0031444	glossoptosis		IAGP		N	RGD:5509061	20221027	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0031449	abnormal nasal cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:33155500
1316996	Med23	mediator complex subunit 23	gene	MP:0031450	nasal cartilage hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:33155500
1316998	Zup1	zinc finger containing ubiquitin peptidase 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20240829	MGI			PMID:38460305
1316998	Zup1	zinc finger containing ubiquitin peptidase 1	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240829	MGI			PMID:38460305
1316998	Zup1	zinc finger containing ubiquitin peptidase 1	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240829	MGI			PMID:38460305
1316999	Mcur1	mitochondrial calcium uniporter regulator 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20171116	MGI			PMID:27184846
1316999	Mcur1	mitochondrial calcium uniporter regulator 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1316999	Mcur1	mitochondrial calcium uniporter regulator 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20171116	MGI			PMID:27184846
1316999	Mcur1	mitochondrial calcium uniporter regulator 1	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20171116	MGI			PMID:27184846
1316999	Mcur1	mitochondrial calcium uniporter regulator 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20171116	MGI			PMID:27184846
1316999	Mcur1	mitochondrial calcium uniporter regulator 1	gene	MP:0011134	decreased lung endothelial cell migration		IAGP		N	RGD:5509061	20171116	MGI			PMID:27184846
1316999	Mcur1	mitochondrial calcium uniporter regulator 1	gene	MP:0011140	decreased lung endothelial cell proliferation		IAGP		N	RGD:5509061	20171116	MGI			PMID:27184846
1317001	Slmap	sarcolemma associated protein	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20111116	MGI			
1317001	Slmap	sarcolemma associated protein	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20240808	MGI			PMID:38474134
1317001	Slmap	sarcolemma associated protein	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38474134
1317001	Slmap	sarcolemma associated protein	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1317001	Slmap	sarcolemma associated protein	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20201022	MGI			
1317001	Slmap	sarcolemma associated protein	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20201022	MGI			
1317001	Slmap	sarcolemma associated protein	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20240808	MGI			PMID:38474134
1317001	Slmap	sarcolemma associated protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317001	Slmap	sarcolemma associated protein	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20201022	MGI			
1317001	Slmap	sarcolemma associated protein	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20201022	MGI			
1317001	Slmap	sarcolemma associated protein	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20240808	MGI			PMID:38474134
1317001	Slmap	sarcolemma associated protein	gene	MP:0031536	decreased heart atrium wall thickness		IAGP		N	RGD:5509061	20240808	MGI			PMID:38474134
1317001	Slmap	sarcolemma associated protein	gene	MP:0031608	decreased fetal cardiomyocyte size		IAGP		N	RGD:5509061	20240808	MGI			PMID:38474134
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15315763
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611729
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002243	abnormal vomeronasal organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002251	abnormal nasopharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002659	pituitary gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004419	absent parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004419	absent parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004440	absent occipital bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0005224	abnormal left-right axis symmetry of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0005315	absent pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20171019	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0008385	absent basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611729
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0010335	fused first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611729
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576405
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372301
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421714
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0012258	philtrum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0013595	absent vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0014106	delayed chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:15269168
1317003	Disp1	dispatched RND transporter family member 1	gene	MP:0030314	absent primary palate		IAGP		N	RGD:5509061	20171109	MGI			PMID:15269168
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20150521	MGI			PMID:24766809
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20150521	MGI			PMID:24766809
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20150521	MGI			PMID:24766809
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20150521	MGI			PMID:24766809
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001080	defasiculated phrenic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20150521	MGI			PMID:24766809
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20150521	MGI			PMID:24766809
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20150521	MGI			PMID:24766809
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20150521	MGI			PMID:24766809
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0009959	abnormal cerebellar hemisphere morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0009980	abnormal cerebellum dentate nucleus morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:23474986
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20211021	MGI			PMID:34548404
1317008	Clp1	CLP1, cleavage and polyadenylation factor I subunit	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:34548404
1317011	Ctsg	cathepsin G	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750176
1317011	Ctsg	cathepsin G	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750176
1317011	Ctsg	cathepsin G	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750176
1317011	Ctsg	cathepsin G	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20647568
1317011	Ctsg	cathepsin G	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750176
1317011	Ctsg	cathepsin G	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20647568
1317011	Ctsg	cathepsin G	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750176
1317011	Ctsg	cathepsin G	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750176
1317011	Ctsg	cathepsin G	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14636558
1317011	Ctsg	cathepsin G	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750176
1317011	Ctsg	cathepsin G	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14636558
1317011	Ctsg	cathepsin G	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20647568
1317011	Ctsg	cathepsin G	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10590073
1317011	Ctsg	cathepsin G	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750176
1317011	Ctsg	cathepsin G	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20647568
1317011	Ctsg	cathepsin G	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750176
1317011	Ctsg	cathepsin G	gene	MP:0004049	increased acute promyelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20647568
1317011	Ctsg	cathepsin G	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20647568
1317011	Ctsg	cathepsin G	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10714686
1317011	Ctsg	cathepsin G	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20647568
1317011	Ctsg	cathepsin G	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:10714686
1317011	Ctsg	cathepsin G	gene	MP:0009787	increased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10714686
1317011	Ctsg	cathepsin G	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10714686
1317012	Ift46	intraflagellar transport 46	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0012093	absent nodal flow		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317012	Ift46	intraflagellar transport 46	gene	MP:0012270	cardiac edema		IAGP		N	RGD:5509061	20160421	MGI			PMID:25722189
1317014	Fcho1	FCH domain only 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1317014	Fcho1	FCH domain only 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1317014	Fcho1	FCH domain only 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20241121	MGI			
1317016	Extl2	exostosin-like glycosyltransferase 2	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395820
1317018	Cavin1	caveolae associated 1	gene	MP:0000741	impaired contractility of urinary bladder detrusor smooth muscle		IAGP		N	RGD:5509061	20150219	MGI			PMID:22643325
1317018	Cavin1	caveolae associated 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20150312	MGI			PMID:24303100
1317018	Cavin1	caveolae associated 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20150312	MGI			PMID:24303100
1317018	Cavin1	caveolae associated 1	gene	MP:0003913	increased heart right ventricle weight		IAGP		N	RGD:5509061	20150312	MGI			PMID:24303100
1317018	Cavin1	caveolae associated 1	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652019
1317018	Cavin1	caveolae associated 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20150312	MGI			PMID:24303100
1317018	Cavin1	caveolae associated 1	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652019
1317018	Cavin1	caveolae associated 1	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20150312	MGI			PMID:22643325
1317018	Cavin1	caveolae associated 1	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20150312	MGI			PMID:24303100
1317018	Cavin1	caveolae associated 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840361
1317018	Cavin1	caveolae associated 1	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652019
1317018	Cavin1	caveolae associated 1	gene	MP:0010758	increased right ventricle systolic pressure		IAGP		N	RGD:5509061	20150312	MGI			PMID:24303100
1317018	Cavin1	caveolae associated 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150219	MGI			PMID:22643325
1317018	Cavin1	caveolae associated 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150219	MGI			PMID:22643325
1317018	Cavin1	caveolae associated 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23652019
1317018	Cavin1	caveolae associated 1	gene	MP:0011774	abnormal urinary bladder detrusor smooth muscle morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:22643325
1317018	Cavin1	caveolae associated 1	gene	MP:0011799	increased urinary bladder weight		IAGP		N	RGD:5509061	20150219	MGI			PMID:22643325
1317018	Cavin1	caveolae associated 1	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20160421	MGI			PMID:18840361
1317021	Isy1	ISY1 splicing factor homolog	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1317021	Isy1	ISY1 splicing factor homolog	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20240926	MGI			
1317021	Isy1	ISY1 splicing factor homolog	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20240926	MGI			
1317021	Isy1	ISY1 splicing factor homolog	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1317021	Isy1	ISY1 splicing factor homolog	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1317021	Isy1	ISY1 splicing factor homolog	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20240926	MGI			
1317021	Isy1	ISY1 splicing factor homolog	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787506
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787506
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787506
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17579027
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17579027
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150890
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573689
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573689
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710223
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846484
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573689
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573689
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573689
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17579027
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573689
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150890
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573689
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442388
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150890
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20240509	MGI			PMID:38457343
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573689
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150890
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573689
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787506
1317024	Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1317030	Kifc3	kinesin family member C3	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20220811	MGI			
1317033	Kif20a	kinesin family member 20A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1317033	Kif20a	kinesin family member 20A	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1317033	Kif20a	kinesin family member 20A	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160421	MGI			
1317033	Kif20a	kinesin family member 20A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20181227	MGI			
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0003914	decreased heart right ventricle weight		IAGP		N	RGD:5509061	20210429	MGI			PMID:30923760
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20260402	MGI			
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0009137	decreased brown fat lipid droplet number		IAGP		N	RGD:5509061	20160218	MGI			PMID:24519944
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20221215	MGI			
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210429	MGI			PMID:30923760
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0010580	decreased heart left ventricle size		IAGP		N	RGD:5509061	20210429	MGI			PMID:30923760
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210429	MGI			PMID:30923760
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317035	Fitm2	fat storage-inducing transmembrane protein 2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210520	MGI			
1317038	Ptpdc1	protein tyrosine phosphatase domain containing 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1317038	Ptpdc1	protein tyrosine phosphatase domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200102	MGI			PMID:26306008
1317038	Ptpdc1	protein tyrosine phosphatase domain containing 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20221215	MGI			
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20221103	MGI			
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20221103	MGI			
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0014190	abnormal epididymis physiology		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0031301	chronic liver inflammation		IAGP		N	RGD:5509061	20211028	MGI			PMID:24332041
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0031425	enhanced male fertility		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0031426	increased sperm motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317044	Ncoa5	nuclear receptor coactivator 5	gene	MP:0031427	increased sperm progressive motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:31664153
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0009673	increased birth weight		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20160505	MGI			PMID:25736226
1317047	Riox1	ribosomal oxygenase 1	gene	MP:0030278	thick neurocranium		IAGP		N	RGD:5509061	20171102	MGI			PMID:25736226
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0004266	pale placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19464366
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517283
1317049	Pak4	p21 (RAC1) activated kinase 4	gene	MP:0021101	abnormal ventral interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:14517283
1317051	Commd9	COMM domain containing 9	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20241121	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160421	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20160421	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317051	Commd9	COMM domain containing 9	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317051	Commd9	COMM domain containing 9	gene	MP:0014012	abnormal cranial blood vasculature morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26553930
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0009877	exostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236767
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116694
1317053	Ext2	exostosin glycosyltransferase 2	gene	MP:0014586	decreased egg cylinder size		IAGP		N	RGD:5509061	20241212	MGI			PMID:16236767
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517553
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000041	absent endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000041	absent endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000041	absent endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000044	absent organ of Corti		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070080
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001072	abnormal vestibulocochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001086	absent petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517553
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517553
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22340499
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002659	pituitary gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517553
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003110	absent malleus processus brevis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003163	absent posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003164	decreased posterior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003164	decreased posterior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003166	decreased superior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003166	decreased superior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003499	thyroid gland hypoplasia		IAGP		N	RGD:5509061	20150122	MGI			PMID:12070080
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003740	fusion of middle ear ossicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004248	abnormal epaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004299	absent vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004314	absent inner ear vestibule		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004315	absent vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004317	small vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004328	decreased vestibular hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004396	decreased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22340499
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22340499
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004427	abnormal vestibular labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004506	abnormal pubis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004507	abnormal ischium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004922	abnormal common crus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005247	abnormal extraocular muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006018	abnormal tympanic membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006284	absent hypaxial muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006285	absent inner ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0006285	absent inner ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0008063	increased otic epithelial cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0008063	increased otic epithelial cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0008064	decreased otic epithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0008065	short endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0008065	short endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678597
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0009707	absent external auditory canal		IAGP		N	RGD:5509061	20170921	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16990542
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0009897	decreased maxillary shelf size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0010466	vascular ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072433
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517553
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0013163	absent thyroid gland isthmus		IAGP		N	RGD:5509061	20150122	MGI			PMID:12070080
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0013222	abnormal first pharyngeal pouch morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0013290	persistent ultimobranchial bodies		IAGP		N	RGD:5509061	20150129	MGI			PMID:12070080
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0030097	preauricular pit		IAGP		N	RGD:5509061	20170928	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0030155	absent tympanic cavity		IAGP		N	RGD:5509061	20171005	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0030161	absent auditory bulla		IAGP		N	RGD:5509061	20171005	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0030204	large nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:10471511
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0030421	tongue muscle hypoplasia		IAGP		N	RGD:5509061	20171214	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0030426	facial muscle hypoplasia		IAGP		N	RGD:5509061	20171214	MGI			PMID:21364285
1317055	Eya1	EYA transcriptional coactivator and phosphatase 1	gene	MP:0031660	prenatal lethality prior to heart atrial septation, incomplete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317062	Rsph1	radial spoke head 1 homolog (Chlamydomonas)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18453535
1317062	Rsph1	radial spoke head 1 homolog (Chlamydomonas)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18453535
1317062	Rsph1	radial spoke head 1 homolog (Chlamydomonas)	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18453535
1317062	Rsph1	radial spoke head 1 homolog (Chlamydomonas)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18453535
1317062	Rsph1	radial spoke head 1 homolog (Chlamydomonas)	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18453535
1317062	Rsph1	radial spoke head 1 homolog (Chlamydomonas)	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18453535
1317062	Rsph1	radial spoke head 1 homolog (Chlamydomonas)	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:18453535
1317062	Rsph1	radial spoke head 1 homolog (Chlamydomonas)	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:18453535
1317062	Rsph1	radial spoke head 1 homolog (Chlamydomonas)	gene	MP:0009852	increased Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20220303	MGI			PMID:18453535
1317064	Naa20	N(alpha)-acetyltransferase 20, NatB catalytic subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20180329	MGI			PMID:28028151
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20240613	MGI			PMID:31405606
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898472
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461490
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0001806	decreased IgM level		IEA		N	RGD:5509061	20141003	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0001830	decreased activated T cell number		IEA		N	RGD:5509061	20141003	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0002144	abnormal B cell differentiation		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0002145	abnormal T cell differentiation		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461490
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180329	MGI			PMID:28028151
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898472
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898472
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461490
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461490
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461490
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898472
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898472
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461490
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008183	absent marginal zone B cells		IEA		N	RGD:5509061	20141003	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008200	decreased follicular dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461490
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19898472
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20180329	MGI			PMID:28028151
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20240613	MGI			PMID:31405606
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1317066	Dock8	dedicator of cytokinesis 8	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20160915	MGI			
1317069	Tbx6	T-box 6	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20200730	MGI			PMID:31888956
1317069	Tbx6	T-box 6	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20200730	MGI			PMID:30307510
1317069	Tbx6	T-box 6	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9490412
1317069	Tbx6	T-box 6	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20260402	MGI			PMID:41636699
1317069	Tbx6	T-box 6	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1317069	Tbx6	T-box 6	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18575602
1317069	Tbx6	T-box 6	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20150205	MGI			PMID:21331042
1317069	Tbx6	T-box 6	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1317069	Tbx6	T-box 6	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:21331042
1317069	Tbx6	T-box 6	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9490412
1317069	Tbx6	T-box 6	gene	MP:0003401	enlarged tail bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:9490412
1317069	Tbx6	T-box 6	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18575602
1317069	Tbx6	T-box 6	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18575602
1317069	Tbx6	T-box 6	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18575602
1317069	Tbx6	T-box 6	gene	MP:0004600	abnormal vertebral transverse process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0004602	abnormal vertebral articular process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20200730	MGI			PMID:30307510
1317069	Tbx6	T-box 6	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20200730	MGI			PMID:31888956
1317069	Tbx6	T-box 6	gene	MP:0004612	fusion of vertebral bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0004669	enlarged vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0004670	small vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20200730	MGI			PMID:30307510
1317069	Tbx6	T-box 6	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0005227	abnormal vertebral body development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0005229	abnormal intervertebral disk development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1317069	Tbx6	T-box 6	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1317069	Tbx6	T-box 6	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9490412
1317069	Tbx6	T-box 6	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:9490412
1317069	Tbx6	T-box 6	gene	MP:0008933	abnormal motile primary cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18575602
1317069	Tbx6	T-box 6	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9490412
1317069	Tbx6	T-box 6	gene	MP:0010662	abnormal intersomitic artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9490412
1317069	Tbx6	T-box 6	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200730	MGI			PMID:30307510
1317069	Tbx6	T-box 6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9490412
1317069	Tbx6	T-box 6	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:4073528
1317069	Tbx6	T-box 6	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18575602
1317069	Tbx6	T-box 6	gene	MP:0012452	increased retrosplenial granular cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1317069	Tbx6	T-box 6	gene	MP:0012465	increased hippocampal fimbria size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1317069	Tbx6	T-box 6	gene	MP:0012475	increased piriform cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1317069	Tbx6	T-box 6	gene	MP:0012477	increased secondary somatosensory cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1317071	Tnip2	TNFAIP3 interacting protein 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16633345
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801521
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10523604
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801521
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160319
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160319
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160319
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160319
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017968
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160319
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017968
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801521
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160319
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160319
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801521
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801521
1317073	Cd3g	CD3 antigen, gamma polypeptide	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160319
1317075	Anxa8	annexin A8	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:24769558
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127460
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127460
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127460
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127460
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0002697	abnormal eye size		IEA		N	RGD:5509061	20160804	MGI			
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127460
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127460
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0009716	abnormal subcommissural organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15494444
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0010167	decreased response to stress-induced hyperthermia		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127460
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0012538	persistent hyaloid artery		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1317077	Socs7	suppressor of cytokine signaling 7	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130239
1317079	Celf1	CUGBP, Elav-like family member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317083	Dsel	dermatan sulfate epimerase-like	gene	MP:0000192	abnormal mineral level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496542
1317083	Dsel	dermatan sulfate epimerase-like	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496542
1317083	Dsel	dermatan sulfate epimerase-like	gene	MP:0014958	decreased lung enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22496542
1317083	Dsel	dermatan sulfate epimerase-like	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22496542
1317083	Dsel	dermatan sulfate epimerase-like	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22496542
1317083	Dsel	dermatan sulfate epimerase-like	gene	MP:0014972	decreased spleen enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22496542
1317083	Dsel	dermatan sulfate epimerase-like	gene	MP:0014975	decreased kidney enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22496542
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200514	MGI			PMID:31600785
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0000373	belly spot		IEA		N	RGD:5509061	20111116	MGI			
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20200514	MGI			PMID:31600785
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002095	abnormal skin pigmentation		IEA		N	RGD:5509061	20171109	MGI			
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002671	belted		IAGP		N	RGD:5509061	20141003	MGI			PMID:10614578
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002671	belted		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925592
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002671	belted		IAGP		N	RGD:5509061	20141003	MGI			PMID:14138974
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002671	belted		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002671	belted		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713933
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:10614578
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20200514	MGI			PMID:31600785
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0002940	variable body spotting		IEA		N	RGD:5509061	20190103	MGI			
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713933
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14138974
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0005072	abnormal hair follicle melanin granule morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0009555	abnormal hair follicle melanin granule distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:14138974
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0009784	abnormal melanoblast migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14138974
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0009784	abnormal melanoblast migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0009874	abnormal interdigital cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0010770	preweaning lethality		IAGP		N	RGD:5509061	20200514	MGI			PMID:31600785
1317085	Adamts20	ADAM metallopeptidase with thrombospondin type 1 motif 20	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317091	Zc3h13	zinc finger CCCH type containing 13	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210520	MGI			
1317093	Nfe2l3	nuclear factor, erythroid derived 2, like 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060151
1317093	Nfe2l3	nuclear factor, erythroid derived 2, like 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060151
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0010129	increased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0012051	spasticity		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0013585	thymus cortex atrophy		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317095	Dnajc11	DnaJ heat shock protein family (Hsp40) member C11	gene	MP:0013590	enlarged thymus medulla		IAGP		N	RGD:5509061	20160225	MGI			PMID:25111180
1317097	Recql4	RecQ protein-like 4	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0000128	growth retardation of molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20230601	MGI			
1317097	Recql4	RecQ protein-like 4	gene	MP:0000413	polyphalangy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0000561	adactyly		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1317097	Recql4	RecQ protein-like 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11979727
1317097	Recql4	RecQ protein-like 4	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0005174	abnormal tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20230601	MGI			
1317097	Recql4	RecQ protein-like 4	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915449
1317097	Recql4	RecQ protein-like 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11979727
1317097	Recql4	RecQ protein-like 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317097	Recql4	RecQ protein-like 4	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11979727
1317097	Recql4	RecQ protein-like 4	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1317097	Recql4	RecQ protein-like 4	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:15703196
1317097	Recql4	RecQ protein-like 4	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317097	Recql4	RecQ protein-like 4	gene	MP:0030358	premature squamoparietal suture closure		IAGP		N	RGD:5509061	20260122	MGI			PMID:25556649
1317101	Tbx1	T-box 1	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0000022	abnormal ear shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0000025	otic hypertelorism		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084464
1317101	Tbx1	T-box 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1317101	Tbx1	T-box 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
1317101	Tbx1	T-box 1	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
1317101	Tbx1	T-box 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913075
1317101	Tbx1	T-box 1	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0000040	decreased middle ear ossicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0000040	decreased middle ear ossicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913075
1317101	Tbx1	T-box 1	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1317101	Tbx1	T-box 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1317101	Tbx1	T-box 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1317101	Tbx1	T-box 1	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
1317101	Tbx1	T-box 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1317101	Tbx1	T-box 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1317101	Tbx1	T-box 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385444
1317101	Tbx1	T-box 1	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0001068	abnormal mandibular nerve branching		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0001068	abnormal mandibular nerve branching		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0001072	abnormal vestibulocochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0001075	abnormal accessory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0001075	abnormal accessory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1317101	Tbx1	T-box 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230119	MGI			
1317101	Tbx1	T-box 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1317101	Tbx1	T-box 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
1317101	Tbx1	T-box 1	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219655
1317101	Tbx1	T-box 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
1317101	Tbx1	T-box 1	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20191010	MGI			
1317101	Tbx1	T-box 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439995
1317101	Tbx1	T-box 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23011393
1317101	Tbx1	T-box 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230119	MGI			
1317101	Tbx1	T-box 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439995
1317101	Tbx1	T-box 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20170413	MGI			
1317101	Tbx1	T-box 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439995
1317101	Tbx1	T-box 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1317101	Tbx1	T-box 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439995
1317101	Tbx1	T-box 1	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20230119	MGI			
1317101	Tbx1	T-box 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1317101	Tbx1	T-box 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:21908517
1317101	Tbx1	T-box 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1317101	Tbx1	T-box 1	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
1317101	Tbx1	T-box 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1317101	Tbx1	T-box 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1317101	Tbx1	T-box 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21107579
1317101	Tbx1	T-box 1	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913075
1317101	Tbx1	T-box 1	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1317101	Tbx1	T-box 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0002253	abnormal pharyngeal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19531352
1317101	Tbx1	T-box 1	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0002263	abnormal laryngeal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385444
1317101	Tbx1	T-box 1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21908517
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317101	Tbx1	T-box 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
1317101	Tbx1	T-box 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12464426
1317101	Tbx1	T-box 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1317101	Tbx1	T-box 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23011393
1317101	Tbx1	T-box 1	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21908517
1317101	Tbx1	T-box 1	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084464
1317101	Tbx1	T-box 1	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1317101	Tbx1	T-box 1	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913075
1317101	Tbx1	T-box 1	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0003395	abnormal subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0003410	abnormal artery development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23011393
1317101	Tbx1	T-box 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:21908517
1317101	Tbx1	T-box 1	gene	MP:0003679	ear lobe hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913075
1317101	Tbx1	T-box 1	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0003756	abnormal hard palate morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0003756	abnormal hard palate morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:30121012
1317101	Tbx1	T-box 1	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23011393
1317101	Tbx1	T-box 1	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21107579
1317101	Tbx1	T-box 1	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1317101	Tbx1	T-box 1	gene	MP:0004038	lymphangiectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439995
1317101	Tbx1	T-box 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1317101	Tbx1	T-box 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239417
1317101	Tbx1	T-box 1	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1317101	Tbx1	T-box 1	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1317101	Tbx1	T-box 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0004159	double aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0004159	double aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0004159	double aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239417
1317101	Tbx1	T-box 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0004161	cervical aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239417
1317101	Tbx1	T-box 1	gene	MP:0004161	cervical aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1317101	Tbx1	T-box 1	gene	MP:0004161	cervical aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004205	absent hyoid bone		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004236	absent masseter muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0004236	absent masseter muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0004238	absent pterygoid muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0004238	absent pterygoid muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
1317101	Tbx1	T-box 1	gene	MP:0004300	abnormal organ of Corti supporting cell morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913075
1317101	Tbx1	T-box 1	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0004311	otic vesicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084464
1317101	Tbx1	T-box 1	gene	MP:0004311	otic vesicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0004314	absent inner ear vestibule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913075
1317101	Tbx1	T-box 1	gene	MP:0004314	absent inner ear vestibule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0004314	absent inner ear vestibule		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0004329	vestibular saccular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
1317101	Tbx1	T-box 1	gene	MP:0004332	utricular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
1317101	Tbx1	T-box 1	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004366	abnormal strial marginal cell morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004420	parietal bone hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004555	pharynx hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0004555	pharynx hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0004555	pharynx hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0004568	fusion of glossopharyngeal and vagus nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0004569	glossopharyngeal nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0004569	glossopharyngeal nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0004572	fusion of basioccipital and basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0004572	fusion of basioccipital and basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0004572	fusion of basioccipital and basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0004572	fusion of basioccipital and basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004612	fusion of vertebral bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004668	absent vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20191010	MGI			
1317101	Tbx1	T-box 1	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0004758	absent strial marginal cells		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20250130	MGI			PMID:30121012
1317101	Tbx1	T-box 1	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004900	absent zygomatic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0004900	absent zygomatic arch		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0004914	absent ultimobranchial body		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0004922	abnormal common crus morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219655
1317101	Tbx1	T-box 1	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
1317101	Tbx1	T-box 1	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0006024	collapsed Reissner membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:24009395
1317101	Tbx1	T-box 1	gene	MP:0006024	collapsed Reissner membrane		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1317101	Tbx1	T-box 1	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439995
1317101	Tbx1	T-box 1	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
1317101	Tbx1	T-box 1	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1317101	Tbx1	T-box 1	gene	MP:0006285	absent inner ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913075
1317101	Tbx1	T-box 1	gene	MP:0006285	absent inner ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0006286	inner ear hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0006286	inner ear hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0006289	otic capsule hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0006339	abnormal third pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0006339	abnormal third pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0006340	abnormal fourth pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0006340	abnormal fourth pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0006340	abnormal fourth pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1317101	Tbx1	T-box 1	gene	MP:0006340	abnormal fourth pharyngeal arch morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:12858556
1317101	Tbx1	T-box 1	gene	MP:0006344	small second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0006344	small second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1317101	Tbx1	T-box 1	gene	MP:0006347	abnormal sixth pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1317101	Tbx1	T-box 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858556
1317101	Tbx1	T-box 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23011393
1317101	Tbx1	T-box 1	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0008304	abnormal organ of Corti supporting cell differentiation		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0008308	small scala media		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0008381	absent gonial bone		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0008382	gonial bone hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:21908517
1317101	Tbx1	T-box 1	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439995
1317101	Tbx1	T-box 1	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16684884
1317101	Tbx1	T-box 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20221006	MGI			PMID:26689739
1317101	Tbx1	T-box 1	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221006	MGI			PMID:26689739
1317101	Tbx1	T-box 1	gene	MP:0009879	abnormal arcus anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858556
1317101	Tbx1	T-box 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858556
1317101	Tbx1	T-box 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20250130	MGI			PMID:30121012
1317101	Tbx1	T-box 1	gene	MP:0009899	hyoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0009912	decreased hyoid bone size		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084464
1317101	Tbx1	T-box 1	gene	MP:0010241	abnormal aortic arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1317101	Tbx1	T-box 1	gene	MP:0010241	abnormal aortic arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1317101	Tbx1	T-box 1	gene	MP:0010326	malleus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0010328	thin malleus neck		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0010356	abnormal second pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
1317101	Tbx1	T-box 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1317101	Tbx1	T-box 1	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1317101	Tbx1	T-box 1	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1317101	Tbx1	T-box 1	gene	MP:0010425	abnormal heart and great vessel attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0010440	anomalous pulmonary venous connection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0010459	supravalvar pulmonary trunk stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239417
1317101	Tbx1	T-box 1	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1317101	Tbx1	T-box 1	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0010487	abnormal right subclavian artery morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1317101	Tbx1	T-box 1	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0010583	abnormal conotruncus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0010584	abnormal conotruncus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971873
1317101	Tbx1	T-box 1	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652707
1317101	Tbx1	T-box 1	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20171109	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0010643	absent fourth pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0010643	absent fourth pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0010644	absent sixth pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0010644	absent sixth pharyngeal arch		IAGP		N	RGD:5509061	20171109	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0010729	absent arcus anterior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0010971	abnormal periosteum morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439995
1317101	Tbx1	T-box 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23971992
1317101	Tbx1	T-box 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556915
1317101	Tbx1	T-box 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1317101	Tbx1	T-box 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0011615	submucous cleft palate		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0011615	submucous cleft palate		IAGP		N	RGD:5509061	20250130	MGI			PMID:30121012
1317101	Tbx1	T-box 1	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20141003	MGI			PMID:22921202
1317101	Tbx1	T-box 1	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:12223416
1317101	Tbx1	T-box 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190012
1317101	Tbx1	T-box 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20191017	MGI			PMID:31550482
1317101	Tbx1	T-box 1	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439995
1317101	Tbx1	T-box 1	gene	MP:0012493	absent pharyngeal arch arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0012721	short neck		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0013174	pharynx stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0013265	abnormal fourth pharyngeal pouch morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0013268	second pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0013270	fourth pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20171116	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20250130	MGI			PMID:30121012
1317101	Tbx1	T-box 1	gene	MP:0013546	cleft soft palate		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0013546	cleft soft palate		IAGP		N	RGD:5509061	20250130	MGI			PMID:30121012
1317101	Tbx1	T-box 1	gene	MP:0014516	abnormal middle ear development		IAGP		N	RGD:5509061	20240912	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:21908517
1317101	Tbx1	T-box 1	gene	MP:0021214	anterior cleft palate		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:26689739
1317101	Tbx1	T-box 1	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0030040	absent facial muscle		IAGP		N	RGD:5509061	20170914	MGI			PMID:16452092
1317101	Tbx1	T-box 1	gene	MP:0030084	tympanic ring hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0030107	incus hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:30121012
1317101	Tbx1	T-box 1	gene	MP:0030179	abnormal oral epithelium morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0030228	absent tubotympanic recess		IAGP		N	RGD:5509061	20171019	MGI			PMID:16600992
1317101	Tbx1	T-box 1	gene	MP:0030334	absent sixth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0030334	absent sixth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0030335	absent third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0030335	absent third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0030340	absent fourth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:11242049
1317101	Tbx1	T-box 1	gene	MP:0030340	absent fourth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0030340	absent fourth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:16914493
1317101	Tbx1	T-box 1	gene	MP:0030340	absent fourth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0030341	fourth pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20171116	MGI			PMID:12858556
1317101	Tbx1	T-box 1	gene	MP:0030341	fourth pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20171116	MGI			PMID:15175244
1317101	Tbx1	T-box 1	gene	MP:0030341	fourth pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20171116	MGI			PMID:16696966
1317101	Tbx1	T-box 1	gene	MP:0030341	fourth pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20171116	MGI			PMID:19855134
1317101	Tbx1	T-box 1	gene	MP:0030351	wide coronal suture		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0030535	abnormal hypoglossal cord morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:15385444
1317101	Tbx1	T-box 1	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1317101	Tbx1	T-box 1	gene	MP:0030872	small cricoid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:11242110
1317101	Tbx1	T-box 1	gene	MP:0030872	small cricoid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:15469978
1317101	Tbx1	T-box 1	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:22371266
1317101	Tbx1	T-box 1	gene	MP:0031461	abnormal palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:26689739
1317101	Tbx1	T-box 1	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:26689739
1317101	Tbx1	T-box 1	gene	MP:0031463	increased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:26689739
1317101	Tbx1	T-box 1	gene	MP:0031510	increased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:23011393
1317105	Syngr4	synaptogyrin 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1317106	Zfp54	zinc finger protein 54	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20201022	MGI			
1317109	Natd1	N-acetyltransferase domain containing 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1317109	Natd1	N-acetyltransferase domain containing 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1317109	Natd1	N-acetyltransferase domain containing 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20200402	MGI			
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:14973274
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:14973274
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14973274
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748359
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20190418	MGI			
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0004692	small pubis		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748359
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20220519	MGI			PMID:20130263
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:14973274
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14973274
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20190418	MGI			
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317113	Pappa	pregnancy-associated plasma protein A	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:20130263
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877477
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877477
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877477
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877477
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0002494	increased IgM level		IEA		N	RGD:5509061	20180222	MGI			
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0004978	decreased B-1 B cell number		IEA		N	RGD:5509061	20190404	MGI			
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833156
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833156
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20201022	MGI			
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20180222	MGI			
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20180222	MGI			
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833156
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833156
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877477
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877477
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11877477
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1317116	Pik3ap1	phosphoinositide-3-kinase adaptor protein 1	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20180222	MGI			
1317117	Cep131	centrosomal protein 131	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20220428	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220428	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220428	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20151231	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160204	MGI			PMID:24415959
1317117	Cep131	centrosomal protein 131	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220428	MGI			PMID:24415959
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20251211	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20251211	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251211	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0001787	pericardial edema		IEA		N	RGD:5509061	20251211	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20251211	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IEA		N	RGD:5509061	20251211	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1317122	Exoc3l4	exocyst complex component 3-like 4	gene	MP:0012270	cardiac edema		IEA		N	RGD:5509061	20251211	MGI			
1317124	Nedd1	neural precursor cell expressed, developmentally down-regulated gene 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1317124	Nedd1	neural precursor cell expressed, developmentally down-regulated gene 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20200514	MGI			
1317124	Nedd1	neural precursor cell expressed, developmentally down-regulated gene 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1317124	Nedd1	neural precursor cell expressed, developmentally down-regulated gene 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1317124	Nedd1	neural precursor cell expressed, developmentally down-regulated gene 1	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1317124	Nedd1	neural precursor cell expressed, developmentally down-regulated gene 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317124	Nedd1	neural precursor cell expressed, developmentally down-regulated gene 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1317128	Wipi1	WD repeat domain, phosphoinositide interacting 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1317128	Wipi1	WD repeat domain, phosphoinositide interacting 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1317128	Wipi1	WD repeat domain, phosphoinositide interacting 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1317128	Wipi1	WD repeat domain, phosphoinositide interacting 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1317128	Wipi1	WD repeat domain, phosphoinositide interacting 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230119	MGI			
1317129	Nepn	nephrocan	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20231207	MGI			
1317132	Sphk2	sphingosine kinase 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363629
1317132	Sphk2	sphingosine kinase 2	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1317132	Sphk2	sphingosine kinase 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1317132	Sphk2	sphingosine kinase 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23995678
1317132	Sphk2	sphingosine kinase 2	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363629
1317132	Sphk2	sphingosine kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1317132	Sphk2	sphingosine kinase 2	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1317132	Sphk2	sphingosine kinase 2	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363629
1317132	Sphk2	sphingosine kinase 2	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23995678
1317132	Sphk2	sphingosine kinase 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1317132	Sphk2	sphingosine kinase 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223773
1317132	Sphk2	sphingosine kinase 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363629
1317132	Sphk2	sphingosine kinase 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1317132	Sphk2	sphingosine kinase 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363629
1317132	Sphk2	sphingosine kinase 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1317132	Sphk2	sphingosine kinase 2	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17947634
1317132	Sphk2	sphingosine kinase 2	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808259
1317132	Sphk2	sphingosine kinase 2	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808259
1317132	Sphk2	sphingosine kinase 2	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808259
1317132	Sphk2	sphingosine kinase 2	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17363629
1317132	Sphk2	sphingosine kinase 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16093248
1317132	Sphk2	sphingosine kinase 2	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1317132	Sphk2	sphingosine kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0012503	increased midbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314531
1317132	Sphk2	sphingosine kinase 2	gene	MP:0014470	abnormal B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:16223773
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230119	MGI			
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002708	nephrolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532086
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002708	nephrolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002708	nephrolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002708	nephrolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002708	nephrolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532086
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003311	aminoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0009645	crystalluria		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0010378	increased respiratory quotient		IEA		N	RGD:5509061	20230601	MGI			
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9776749
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532086
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011403	pyelonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011413	colorless urine		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011422	kidney medulla atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011423	kidney cortex atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011424	decreased urine uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011477	abnormal urine nucleoside level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105024
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011477	abnormal urine nucleoside level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011477	abnormal urine nucleoside level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864750
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011625	cystolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532086
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011625	cystolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643571
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011844	kidney collecting duct atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532086
1317134	Aprt	adenine phosphoribosyl transferase	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689017
1317136	Nemf	nuclear export mediator factor	gene	MP:0000958	peripheral nervous system degeneration		IAGP		N	RGD:5509061	20210715	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210722	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210715	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20210715	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20220120	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20181227	MGI			
1317136	Nemf	nuclear export mediator factor	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20210715	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20210722	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1317136	Nemf	nuclear export mediator factor	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20210715	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1317136	Nemf	nuclear export mediator factor	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20210722	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1317136	Nemf	nuclear export mediator factor	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20210715	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20210722	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20210722	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20220120	MGI			PMID:32934225
1317136	Nemf	nuclear export mediator factor	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20210722	MGI			PMID:32934225
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12660172
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0002050	increased pheochromocytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12660172
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12660172
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12660172
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:16061652
1317139	Hmgn1	high mobility group nucleosomal binding domain 1	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20211021	MGI			
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20200514	MGI			
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:25203538
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0003660	chylothorax		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0003660	chylothorax		IAGP		N	RGD:5509061	20160915	MGI			PMID:25203538
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0004038	lymphangiectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20160915	MGI			PMID:25203538
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:25203538
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:25203538
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0010820	abnormal pleura morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566878
1317144	Elk3	ETS transcription factor ELK3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160915	MGI			PMID:25203538
1317146	Cmtm6	CKLF-like MARVEL transmembrane domain containing 6	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20210401	MGI			PMID:32908139
1317146	Cmtm6	CKLF-like MARVEL transmembrane domain containing 6	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20210401	MGI			PMID:32908139
1317146	Cmtm6	CKLF-like MARVEL transmembrane domain containing 6	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20210401	MGI			PMID:32908139
1317146	Cmtm6	CKLF-like MARVEL transmembrane domain containing 6	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:32908139
1317146	Cmtm6	CKLF-like MARVEL transmembrane domain containing 6	gene	MP:0005572	abnormal pulmonary respiratory rate		IAGP		N	RGD:5509061	20210401	MGI			PMID:32908139
1317146	Cmtm6	CKLF-like MARVEL transmembrane domain containing 6	gene	MP:0011994	increased nerve conduction velocity		IAGP		N	RGD:5509061	20210401	MGI			PMID:32908139
1317148	Gan	giant axonal neuropathy	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16303566
1317148	Gan	giant axonal neuropathy	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18680552
1317148	Gan	giant axonal neuropathy	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18680552
1317148	Gan	giant axonal neuropathy	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18680552
1317148	Gan	giant axonal neuropathy	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18680552
1317148	Gan	giant axonal neuropathy	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317148	Gan	giant axonal neuropathy	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565160
1317149	Mfsd6l	major facilitator superfamily domain containing 6-like	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20241226	MGI			PMID:38909778
1317149	Mfsd6l	major facilitator superfamily domain containing 6-like	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20241226	MGI			PMID:38909778
1317149	Mfsd6l	major facilitator superfamily domain containing 6-like	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20241226	MGI			PMID:38909778
1317149	Mfsd6l	major facilitator superfamily domain containing 6-like	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20241226	MGI			PMID:38909778
1317149	Mfsd6l	major facilitator superfamily domain containing 6-like	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20241226	MGI			PMID:38909778
1317149	Mfsd6l	major facilitator superfamily domain containing 6-like	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20241226	MGI			PMID:38909778
1317149	Mfsd6l	major facilitator superfamily domain containing 6-like	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20241226	MGI			PMID:38909778
1317149	Mfsd6l	major facilitator superfamily domain containing 6-like	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20241226	MGI			PMID:38909778
1317149	Mfsd6l	major facilitator superfamily domain containing 6-like	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20241226	MGI			PMID:38909778
1317151	Tm9sf4	transmembrane 9 superfamily member 4	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1317151	Tm9sf4	transmembrane 9 superfamily member 4	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1317151	Tm9sf4	transmembrane 9 superfamily member 4	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1317151	Tm9sf4	transmembrane 9 superfamily member 4	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1317151	Tm9sf4	transmembrane 9 superfamily member 4	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20141003	MGI			
1317151	Tm9sf4	transmembrane 9 superfamily member 4	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1317151	Tm9sf4	transmembrane 9 superfamily member 4	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1317151	Tm9sf4	transmembrane 9 superfamily member 4	gene	MP:0010099	abnormal thoracic cage shape		IEA		N	RGD:5509061	20150430	MGI			
1317151	Tm9sf4	transmembrane 9 superfamily member 4	gene	MP:0012725	small sebaceous gland		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0011281	abnormal olfactory epithelium cilium morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:21646512
1317153	Ttc8	tetratricopeptide repeat domain 8	gene	MP:0014749	abnormal olfactory bulb axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:21646512
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1317155	Gga1	golgi associated, gamma adaptin ear containing, ARF binding protein 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20220721	MGI			PMID:34150743
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20220721	MGI			PMID:34150743
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20220811	MGI			
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20250508	MGI			
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20220519	MGI			
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0009263	abnormal eyelid fusion		IEA		N	RGD:5509061	20250508	MGI			
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20220721	MGI			PMID:34150743
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0010099	abnormal thoracic cage shape		IEA		N	RGD:5509061	20220811	MGI			
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20250508	MGI			
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:34150743
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24025402
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:34150743
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20141003	MGI			PMID:24025402
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0015006	decreased fetal length		IAGP		N	RGD:5509061	20260611	MGI			PMID:34150743
1317156	Wiz	widely-interspaced zinc finger motifs	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20220721	MGI			PMID:34150743
1317160	Nup37	nucleoporin 37	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20240523	MGI			
1317160	Nup37	nucleoporin 37	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1317160	Nup37	nucleoporin 37	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20181227	MGI			
1317160	Nup37	nucleoporin 37	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1317164	Opalin	oligodendrocytic myelin paranodal and inner loop protein	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20190926	MGI			PMID:27855200
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20181227	MGI			
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737267
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737267
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737267
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737267
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737267
1317166	Rbms1	RNA binding motif, single stranded interacting protein 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737267
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0000650	mesocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20141003	MGI			
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0004403	absent cochlear outer hair cells		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0005330	cardiomyopathy		IEA		N	RGD:5509061	20141003	MGI			
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0011061	abnormal inner hair cell kinocilium morphology		IAGP		N	RGD:5509061	20170907	MGI			PMID:26469318
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317169	Rfx3	regulatory factor X, 3 (influences HLA class II expression)	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121860
1317173	Cdkn3	cyclin dependent kinase inhibitor 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1317173	Cdkn3	cyclin dependent kinase inhibitor 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1317176	Ccne2	cyclin E2	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21944720
1317176	Ccne2	cyclin E2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21944720
1317176	Ccne2	cyclin E2	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21944720
1317176	Ccne2	cyclin E2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21944720
1317176	Ccne2	cyclin E2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:21944720
1317176	Ccne2	cyclin E2	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21944720
1317176	Ccne2	cyclin E2	gene	MP:0010241	abnormal aortic arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970191
1317176	Ccne2	cyclin E2	gene	MP:0014379	decreased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:21944720
1317176	Ccne2	cyclin E2	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:12941272
1317176	Ccne2	cyclin E2	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:21944720
1317178	Prpf4b	pre-mRNA processing factor 4B	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241017	MGI			
1317178	Prpf4b	pre-mRNA processing factor 4B	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191205	MGI			
1317178	Prpf4b	pre-mRNA processing factor 4B	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241017	MGI			
1317178	Prpf4b	pre-mRNA processing factor 4B	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20191205	MGI			
1317178	Prpf4b	pre-mRNA processing factor 4B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317178	Prpf4b	pre-mRNA processing factor 4B	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20191205	MGI			
1317178	Prpf4b	pre-mRNA processing factor 4B	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1317182	Snx20	sorting nexin 20	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18196517
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0000923	abnormal roof plate morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0008409	increased cellular sensitivity to hydroxyurea induced cell death		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0010250	absent thymus cortex		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317191	Pole4	polymerase (DNA-directed), epsilon 4 (p12 subunit)	gene	MP:0030049	prominent forehead		IAGP		N	RGD:5509061	20180712	MGI			PMID:29754823
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936253
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20141003	MGI			
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180517	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936253
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936253
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936253
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936253
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:16936253
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936253
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936253
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160804	MGI			
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840758
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20180517	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20180125	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20190711	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:28737513
1317193	Bag3	BCL2-associated athanogene 3	gene	MP:0031645	increased myocardial fiber apoptosis		IAGP		N	RGD:5509061	20250515	MGI			PMID:16936253
1317195	Zfyve1	zinc finger, FYVE domain containing 1	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20200924	MGI			PMID:32251420
1317195	Zfyve1	zinc finger, FYVE domain containing 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1317195	Zfyve1	zinc finger, FYVE domain containing 1	gene	MP:0009790	decreased susceptibility to viral infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200924	MGI			PMID:32251420
1317197	Igsf3	immunoglobulin superfamily, member 3	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:37821496
1317197	Igsf3	immunoglobulin superfamily, member 3	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:37821496
1317197	Igsf3	immunoglobulin superfamily, member 3	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20240516	MGI			PMID:37821496
1317197	Igsf3	immunoglobulin superfamily, member 3	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:37821496
1317197	Igsf3	immunoglobulin superfamily, member 3	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20240516	MGI			PMID:37821496
1317197	Igsf3	immunoglobulin superfamily, member 3	gene	MP:0013007	abnormal vagal neural crest cell migration		IAGP		N	RGD:5509061	20240516	MGI			PMID:37821496
1317201	Ist1	increased sodium tolerance 1 homolog (yeast)	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1317201	Ist1	increased sodium tolerance 1 homolog (yeast)	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210520	MGI			
1317201	Ist1	increased sodium tolerance 1 homolog (yeast)	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
1317201	Ist1	increased sodium tolerance 1 homolog (yeast)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317203	Apobec3	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055735
1317203	Apobec3	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18772436
1317203	Apobec3	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:286744
1317203	Apobec3	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17259974
1317203	Apobec3	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18772436
1317203	Apobec3	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3	gene	MP:0020935	decreased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:286744
1317203	Apobec3	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3	gene	MP:0031038	increased susceptibility to Retroviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:18772436
1317205	Cmtr1	cap methyltransferase 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:33086056
1317205	Cmtr1	cap methyltransferase 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20210211	MGI			PMID:33086056
1317205	Cmtr1	cap methyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317205	Cmtr1	cap methyltransferase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1317205	Cmtr1	cap methyltransferase 1	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20210211	MGI			PMID:33086056
1317205	Cmtr1	cap methyltransferase 1	gene	MP:0020912	abnormal susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20210211	MGI			PMID:33086056
1317207	Noxo1	NADPH oxidase organizer 1	gene	MP:0001394	circling		IEA		N	RGD:5509061	20111116	MGI			
1317207	Noxo1	NADPH oxidase organizer 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16431374
1317207	Noxo1	NADPH oxidase organizer 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16431374
1317207	Noxo1	NADPH oxidase organizer 1	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16431374
1317207	Noxo1	NADPH oxidase organizer 1	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:16431374
1317207	Noxo1	NADPH oxidase organizer 1	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:16431374
1317208	Herc3	hect domain and RLD 3	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160804	MGI			
1317208	Herc3	hect domain and RLD 3	gene	MP:0001391	abnormal tail movements		IEA		N	RGD:5509061	20160804	MGI			
1317208	Herc3	hect domain and RLD 3	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20160804	MGI			
1317208	Herc3	hect domain and RLD 3	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1317208	Herc3	hect domain and RLD 3	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20160804	MGI			
1317208	Herc3	hect domain and RLD 3	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615570
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615570
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22615570
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24014876
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0020155	enhanced humoral immune response		IAGP		N	RGD:5509061	20191226	MGI			PMID:26263558
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:22615570
1317210	Ifit2	interferon-induced protein with tetratricopeptide repeats 2	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:22615570
1317212	Fam209	family with sequence similarity 209	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1317212	Fam209	family with sequence similarity 209	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:34471926
1317212	Fam209	family with sequence similarity 209	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:34471926
1317212	Fam209	family with sequence similarity 209	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220224	MGI			PMID:34471926
1317212	Fam209	family with sequence similarity 209	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220224	MGI			PMID:34471926
1317212	Fam209	family with sequence similarity 209	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20220224	MGI			PMID:34471926
1317212	Fam209	family with sequence similarity 209	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:34471926
1317215	Rnf19a	ring finger protein 19A	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20180712	MGI			PMID:26553645
1317215	Rnf19a	ring finger protein 19A	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20180712	MGI			PMID:26553645
1317215	Rnf19a	ring finger protein 19A	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20180712	MGI			PMID:26553645
1317215	Rnf19a	ring finger protein 19A	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20180712	MGI			PMID:26553645
1317215	Rnf19a	ring finger protein 19A	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20180712	MGI			PMID:26553645
1317215	Rnf19a	ring finger protein 19A	gene	MP:0009938	abnormal hippocampus granule cell morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:26553645
1317215	Rnf19a	ring finger protein 19A	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20180712	MGI			PMID:26553645
1317217	Efna4	ephrin A4	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20181227	MGI			
1317217	Efna4	ephrin A4	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1317217	Efna4	ephrin A4	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1317217	Efna4	ephrin A4	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20220519	MGI			
1317217	Efna4	ephrin A4	gene	MP:0011471	decreased urine creatinine level		IEA		N	RGD:5509061	20240523	MGI			
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20171214	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626504
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0003840	abnormal coronal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0003843	abnormal sagittal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0004420	parietal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0030387	large posterior fontanelle		IAGP		N	RGD:5509061	20171214	MGI			PMID:17567669
1317221	Itgb1bp1	integrin beta 1 binding protein 1	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20171214	MGI			PMID:17567669
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0002174	abnormal gastrulation movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0005224	abnormal left-right axis symmetry of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317223	Supt20	SPT20 SAGA complex component	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751104
1317225	Dnajc10	DnaJ heat shock protein family (Hsp40) member C10	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20170323	MGI			
1317225	Dnajc10	DnaJ heat shock protein family (Hsp40) member C10	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20170323	MGI			
1317225	Dnajc10	DnaJ heat shock protein family (Hsp40) member C10	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20170323	MGI			
1317225	Dnajc10	DnaJ heat shock protein family (Hsp40) member C10	gene	MP:0005310	abnormal salivary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19788412
1317225	Dnajc10	DnaJ heat shock protein family (Hsp40) member C10	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1317225	Dnajc10	DnaJ heat shock protein family (Hsp40) member C10	gene	MP:0012322	decreased total tissue mass		IEA		N	RGD:5509061	20170323	MGI			
1317225	Dnajc10	DnaJ heat shock protein family (Hsp40) member C10	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20161013	MGI			PMID:19788412
1317231	Drc4	dynein regulatory complex subunit 4	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20161103	MGI			PMID:27472056
1317231	Drc4	dynein regulatory complex subunit 4	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:27472056
1317231	Drc4	dynein regulatory complex subunit 4	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20161103	MGI			PMID:27472056
1317231	Drc4	dynein regulatory complex subunit 4	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20161103	MGI			PMID:27472056
1317231	Drc4	dynein regulatory complex subunit 4	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20161103	MGI			PMID:27472056
1317231	Drc4	dynein regulatory complex subunit 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161103	MGI			PMID:27472056
1317231	Drc4	dynein regulatory complex subunit 4	gene	MP:0011253	situs inversus with levocardia		IAGP		N	RGD:5509061	20161103	MGI			PMID:27472056
1317233	Hint1	histidine triad nucleotide binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810953
1317233	Hint1	histidine triad nucleotide binding protein 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748294
1317233	Hint1	histidine triad nucleotide binding protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748294
1317233	Hint1	histidine triad nucleotide binding protein 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1317233	Hint1	histidine triad nucleotide binding protein 1	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810953
1317233	Hint1	histidine triad nucleotide binding protein 1	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20211104	MGI			PMID:33953175
1317233	Hint1	histidine triad nucleotide binding protein 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810953
1317233	Hint1	histidine triad nucleotide binding protein 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1317233	Hint1	histidine triad nucleotide binding protein 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:12810953
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0002804	abnormal motor learning		IEA		N	RGD:5509061	20211021	MGI			
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0002946	delayed axon extension		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0010386	abnormal urinary bladder physiology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20220519	MGI			
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0011874	enlarged urinary bladder		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317237	Zfyve26	zinc finger, FYVE domain containing 26	gene	MP:0012506	brain atrophy		IAGP		N	RGD:5509061	20160304	MGI			PMID:24367272
1317244	Polr1f	RNA polymerase I subunit F	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1317244	Polr1f	RNA polymerase I subunit F	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1317244	Polr1f	RNA polymerase I subunit F	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20260402	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1317246	Kif13a	kinesin family member 13A	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20210826	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23438369
1317246	Kif13a	kinesin family member 13A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23438369
1317246	Kif13a	kinesin family member 13A	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210826	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1317246	Kif13a	kinesin family member 13A	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23438369
1317246	Kif13a	kinesin family member 13A	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210826	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23438369
1317246	Kif13a	kinesin family member 13A	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210826	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1317246	Kif13a	kinesin family member 13A	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20220811	MGI			
1317246	Kif13a	kinesin family member 13A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1317250	Nup133	nucleoporin 133	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1317250	Nup133	nucleoporin 133	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1317250	Nup133	nucleoporin 133	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539113
1317250	Nup133	nucleoporin 133	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317250	Nup133	nucleoporin 133	gene	MP:0012183	decreased paraxial mesoderm size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1317250	Nup133	nucleoporin 133	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1317252	Irf7	interferon regulatory factor 7	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1317252	Irf7	interferon regulatory factor 7	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20351692
1317252	Irf7	interferon regulatory factor 7	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800576
1317252	Irf7	interferon regulatory factor 7	gene	MP:0008563	decreased interferon-alpha secretion		IEA		N	RGD:5509061	20111116	MGI			
1317252	Irf7	interferon regulatory factor 7	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20351692
1317252	Irf7	interferon regulatory factor 7	gene	MP:0008576	decreased circulating interferon-beta level		IEA		N	RGD:5509061	20150305	MGI			
1317252	Irf7	interferon regulatory factor 7	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20351692
1317252	Irf7	interferon regulatory factor 7	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800576
1317252	Irf7	interferon regulatory factor 7	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:15800576
1317252	Irf7	interferon regulatory factor 7	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:20351692
1317252	Irf7	interferon regulatory factor 7	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:15800576
1317252	Irf7	interferon regulatory factor 7	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:26329040
1317252	Irf7	interferon regulatory factor 7	gene	MP:0020952	increased susceptibility to Paramyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:20351692
1317252	Irf7	interferon regulatory factor 7	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:26329040
1317256	Nelfb	negative elongation factor complex member B	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340312
1317256	Nelfb	negative elongation factor complex member B	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340312
1317256	Nelfb	negative elongation factor complex member B	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340312
1317256	Nelfb	negative elongation factor complex member B	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340312
1317256	Nelfb	negative elongation factor complex member B	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340312
1317256	Nelfb	negative elongation factor complex member B	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340312
1317258	Nrsn1	neurensin 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1317258	Nrsn1	neurensin 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1317258	Nrsn1	neurensin 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201231	MGI			
1317258	Nrsn1	neurensin 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1317258	Nrsn1	neurensin 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1317258	Nrsn1	neurensin 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1317262	Wsb1	WD repeat and SOCS box-containing 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20241212	MGI			PMID:38325552
1317262	Wsb1	WD repeat and SOCS box-containing 1	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:38325552
1317262	Wsb1	WD repeat and SOCS box-containing 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20241212	MGI			PMID:38325552
1317262	Wsb1	WD repeat and SOCS box-containing 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20241212	MGI			PMID:38325552
1317262	Wsb1	WD repeat and SOCS box-containing 1	gene	MP:0012196	abnormal myofibroblast differentiation		IAGP		N	RGD:5509061	20241212	MGI			PMID:38325552
1317264	Zfp212	Zinc finger protein 212	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20211216	MGI			PMID:34815492
1317264	Zfp212	Zinc finger protein 212	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20211216	MGI			PMID:34815492
1317264	Zfp212	Zinc finger protein 212	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20211216	MGI			PMID:34815492
1317264	Zfp212	Zinc finger protein 212	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20211216	MGI			PMID:34815492
1317264	Zfp212	Zinc finger protein 212	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20211216	MGI			PMID:34815492
1317264	Zfp212	Zinc finger protein 212	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20211216	MGI			PMID:34815492
1317264	Zfp212	Zinc finger protein 212	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1317264	Zfp212	Zinc finger protein 212	gene	MP:0020870	decreased thigmotaxis		IAGP		N	RGD:5509061	20211216	MGI			PMID:34815492
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20231221	MGI			PMID:15936750
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482960
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482960
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20240104	MGI			PMID:15936750
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0002748	abnormal pulmonary valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0009408	decreased skeletal muscle fiber density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482960
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0010620	thick mitral valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0010620	thick mitral valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:15936750
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0010629	thick tricuspid valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:14993236
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482960
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0031558	tricuspid valve hyperplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:15936750
1317266	Adam12	ADAM metallopeptidase domain 12	gene	MP:0031581	semilunar valve hyperplasia		IAGP		N	RGD:5509061	20240125	MGI			PMID:15936750
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20201022	MGI			PMID:32510560
1317268	Scaper	S phase cyclin A-associated protein in the ER	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:32510560
1317271	Mfap4	microfibrillar-associated protein 4	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1317271	Mfap4	microfibrillar-associated protein 4	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26033354
1317271	Mfap4	microfibrillar-associated protein 4	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20160818	MGI			PMID:26033354
1317271	Mfap4	microfibrillar-associated protein 4	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20160818	MGI			PMID:26033354
1317271	Mfap4	microfibrillar-associated protein 4	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26033354
1317271	Mfap4	microfibrillar-associated protein 4	gene	MP:0010937	increased total lung capacity		IAGP		N	RGD:5509061	20160818	MGI			PMID:26033354
1317271	Mfap4	microfibrillar-associated protein 4	gene	MP:0011045	decreased lung elastance		IAGP		N	RGD:5509061	20160818	MGI			PMID:26033354
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15311277
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:15311277
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15311277
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0010895	increased lung compliance		IEA		N	RGD:5509061	20260402	MGI			
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15311277
1317274	Pias1	protein inhibitor of activated STAT 1	gene	MP:0031023	decreased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:15311277
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20241121	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20241121	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20241121	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380713
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0000746	weakness		IEA		N	RGD:5509061	20111116	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20111116	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380713
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0001504	abnormal posture		IEA		N	RGD:5509061	20111116	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380713
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380713
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380713
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20241121	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380713
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20241121	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:16380713
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20250508	MGI			
1317275	Trak1	trafficking protein, kinesin binding 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20241121	MGI			
1317277	Ldlrad3	low density lipoprotein receptor class A domain containing 3	gene	MP:0020941	decreased susceptibility to Togaviridae infection		IAGP		N	RGD:5509061	20210325	MGI			PMID:33208938
1317281	Usp33	ubiquitin specific peptidase 33	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1317281	Usp33	ubiquitin specific peptidase 33	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1317281	Usp33	ubiquitin specific peptidase 33	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20160804	MGI			
1317281	Usp33	ubiquitin specific peptidase 33	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20160804	MGI			
1317281	Usp33	ubiquitin specific peptidase 33	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1317281	Usp33	ubiquitin specific peptidase 33	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1317283	Zfp395	zinc finger protein 395	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200402	MGI			
1317283	Zfp395	zinc finger protein 395	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1317283	Zfp395	zinc finger protein 395	gene	MP:0010571	shortened ST segment		IEA		N	RGD:5509061	20200402	MGI			
1317283	Zfp395	zinc finger protein 395	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20200402	MGI			
1317283	Zfp395	zinc finger protein 395	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1317288	Gpr87	G protein-coupled receptor 87	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20141003	MGI			
1317288	Gpr87	G protein-coupled receptor 87	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1317288	Gpr87	G protein-coupled receptor 87	gene	MP:0004610	small vertebrae		IEA		N	RGD:5509061	20141003	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20231207	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20240523	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20231207	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20231207	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20170420	MGI			PMID:28355569
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20170420	MGI			PMID:28355569
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20170420	MGI			PMID:28355569
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20170420	MGI			PMID:28355569
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20160331	MGI			PMID:26985035
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20170420	MGI			PMID:28355569
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:31557132
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200402	MGI			PMID:31557132
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170420	MGI			PMID:28355569
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20260402	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20240523	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982418
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20231207	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982418
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982418
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20200402	MGI			PMID:31557132
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002913	abnormal PNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982418
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002913	abnormal PNS synaptic transmission		IAGP		N	RGD:5509061	20160331	MGI			PMID:26985035
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20160331	MGI			PMID:26985035
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20160331	MGI			PMID:26985035
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982418
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982418
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982418
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20170420	MGI			PMID:28355569
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:31557132
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982418
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200402	MGI			PMID:31557132
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20170420	MGI			PMID:28355569
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20200402	MGI			PMID:31557132
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20170420	MGI			PMID:28355569
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0009428	decreased tibialis anterior weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160331	MGI			PMID:26985035
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200402	MGI			PMID:31557132
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982418
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144914
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20240523	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20241121	MGI			
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0014587	impaired fine motor coordination		IAGP		N	RGD:5509061	20241219	MGI			PMID:19470612
1317293	Gars1	glycyl-tRNA synthetase 1	gene	MP:0014603	neuromuscular synapse degeneration		IAGP		N	RGD:5509061	20250206	MGI			PMID:16982418
1317295	Rnf121	ring finger protein 121	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20260402	MGI			
1317295	Rnf121	ring finger protein 121	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20240523	MGI			
1317297	Trim29	tripartite motif-containing 29	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20250605	MGI			PMID:31048544
1317297	Trim29	tripartite motif-containing 29	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250605	MGI			PMID:31048544
1317297	Trim29	tripartite motif-containing 29	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1317297	Trim29	tripartite motif-containing 29	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0008562	increased interferon-alpha secretion		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1317297	Trim29	tripartite motif-containing 29	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1317297	Trim29	tripartite motif-containing 29	gene	MP:0010091	decreased circulating creatine kinase level		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0011393	decreased fetal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0012416	decreased gland tumor incidence		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
1317297	Trim29	tripartite motif-containing 29	gene	MP:0013662	decreased myeloid cell number		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0014435	increased interferon level		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0014438	decreased interleukin level		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0020938	decreased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0031039	decreased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0031601	decreased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20240718	MGI			PMID:38664417
1317297	Trim29	tripartite motif-containing 29	gene	MP:0031705	increased interferon type I secretion		IAGP		N	RGD:5509061	20260402	MGI			PMID:38664417
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20210128	MGI			
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210128	MGI			
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20210128	MGI			
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1317298	Fbxw16	F-box and WD-40 domain protein 16	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20210826	MGI			
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20201022	MGI			
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040848
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040848
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040848
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040848
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040848
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040848
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20190502	MGI			
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0014711	decreased synaptic vesicle readily releasable pool size		IAGP		N	RGD:5509061	20250814	MGI			PMID:21040848
1317300	Napb	N-ethylmaleimide sensitive fusion protein attachment protein beta	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1317304	Pycr1	pyrroline-5-carboxylate reductase 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1317304	Pycr1	pyrroline-5-carboxylate reductase 1	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20230601	MGI			
1317304	Pycr1	pyrroline-5-carboxylate reductase 1	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20240509	MGI			PMID:36495058
1317304	Pycr1	pyrroline-5-carboxylate reductase 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1317304	Pycr1	pyrroline-5-carboxylate reductase 1	gene	MP:0031216	decreased susceptibility to myocardial ischemic injury		IAGP		N	RGD:5509061	20240509	MGI			PMID:36495058
1317306	Gatb	glutamyl-tRNA amidotransferase subunit B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20181227	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20181227	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20210128	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20181227	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20211021	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20181227	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20181227	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1317315	Fbxo36	F-box protein 36	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1317318	Sema4b	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270411
1317318	Sema4b	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270411
1317318	Sema4b	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B	gene	MP:0004041	increased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20161201	MGI			PMID:25892012
1317318	Sema4b	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270411
1317318	Sema4b	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20161201	MGI			PMID:25892012
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20240523	MGI			
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0001670	abnormal intestinal mineral absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17954933
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20250508	MGI			
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20250508	MGI			
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17954933
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17954933
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0009615	abnormal zinc homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17954933
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17954933
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20220811	MGI			
1317320	Slc30a7	solute carrier family 30 (zinc transporter), member 7	gene	MP:0031172	decreased circulating zinc level		IAGP		N	RGD:5509061	20201119	MGI			PMID:17954933
1317325	Lactb2	lactamase, beta 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0013317	abnormal seminal vesicle development		IAGP		N	RGD:5509061	20141204	MGI			PMID:12374767
1317325	Lactb2	lactamase, beta 2	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:12374767
1317326	Prss54	serine protease 54	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20210520	MGI			
1317326	Prss54	serine protease 54	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1317326	Prss54	serine protease 54	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1317326	Prss54	serine protease 54	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1317326	Prss54	serine protease 54	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1317326	Prss54	serine protease 54	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1317326	Prss54	serine protease 54	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20230202	MGI			PMID:35863763
1317326	Prss54	serine protease 54	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20240523	MGI			
1317326	Prss54	serine protease 54	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20210520	MGI			
1317326	Prss54	serine protease 54	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20240523	MGI			
1317326	Prss54	serine protease 54	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20230202	MGI			PMID:35863763
1317326	Prss54	serine protease 54	gene	MP:0013519	decreased CD4-positive NK T cell number		IEA		N	RGD:5509061	20240523	MGI			
1317326	Prss54	serine protease 54	gene	MP:0013522	decreased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20240523	MGI			
1317326	Prss54	serine protease 54	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20230202	MGI			PMID:35863763
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20180111	MGI			PMID:27480224
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20191010	MGI			PMID:26746789
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20180111	MGI			PMID:27480224
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20180111	MGI			PMID:27480224
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20191010	MGI			PMID:26746789
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20180111	MGI			PMID:27480224
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:27480224
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0003191	abnormal cellular cholesterol metabolism		IAGP		N	RGD:5509061	20150416	MGI			PMID:25066056
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:26746789
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:26746789
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20150416	MGI			PMID:25066056
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150416	MGI			PMID:25066056
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20180111	MGI			PMID:27480224
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20180111	MGI			PMID:27480224
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20180111	MGI			PMID:27480224
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20180111	MGI			PMID:27480224
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20150416	MGI			PMID:25066056
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20191010	MGI			PMID:26746789
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20191010	MGI			PMID:26746789
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011131	abnormal lung endothelial cell physiology		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011140	decreased lung endothelial cell proliferation		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011141	increased lung endothelial cell apoptosis		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0012201	decreased endothelial cell proliferation		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0020321	increased vascular endothelial cell apoptosis		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0020517	abnormal visceral yolk sac physiology		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317329	Nus1	NUS1 dehydrodolichyl diphosphate synthase subunit	gene	MP:0020830	abnormal jugular lymph sac morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:26755743
1317331	B4galt4	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 4	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1317336	Fastkd2	FAST kinase domains 2	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200402	MGI			
1317336	Fastkd2	FAST kinase domains 2	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20220519	MGI			
1317336	Fastkd2	FAST kinase domains 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1317336	Fastkd2	FAST kinase domains 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:23393161
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23393161
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23393161
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23393161
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23393161
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23393161
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23393161
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:23393161
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0020237	increased proline level		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:26924217
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0030658	increased glycine level		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0030691	increased serine level		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317338	Twnk	twinkle mtDNA helicase	gene	MP:0030743	decreased aspartic acid level		IAGP		N	RGD:5509061	20250828	MGI			PMID:32737078
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826270
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826270
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0001788	periorbital edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826270
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20181227	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0003390	lymphedema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826270
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20210520	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0004106	lymphatic vessel hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826270
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20181227	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20181227	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1317340	Ptpn14	protein tyrosine phosphatase, non-receptor type 14	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1317342	Ube2d1	ubiquitin-conjugating enzyme E2D 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1317342	Ube2d1	ubiquitin-conjugating enzyme E2D 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20200514	MGI			
1317342	Ube2d1	ubiquitin-conjugating enzyme E2D 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1317342	Ube2d1	ubiquitin-conjugating enzyme E2D 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20181011	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20181011	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20181011	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20181011	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20181011	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0010767	abnormal female meiosis I arrest		IAGP		N	RGD:5509061	20181011	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0011120	increased primordial ovarian follicle number		IAGP		N	RGD:5509061	20181011	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0014447	impaired spindle assembly in female meiosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:29661911
1317343	Patl2	protein associated with topoisomerase II homolog 2 (yeast)	gene	MP:0031014	polyspermy		IAGP		N	RGD:5509061	20200130	MGI			PMID:29661911
1317347	Mynn	myoneurin	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1317347	Mynn	myoneurin	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210520	MGI			
1317347	Mynn	myoneurin	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1317347	Mynn	myoneurin	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1317347	Mynn	myoneurin	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1317347	Mynn	myoneurin	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210826	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1317350	Adipor2	adiponectin receptor 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20200402	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0001154	seminiferous tubule degeneration		IEA		N	RGD:5509061	20111116	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0001156	abnormal spermatogenesis		IEA		N	RGD:5509061	20111116	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20170105	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1317350	Adipor2	adiponectin receptor 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230601	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1317350	Adipor2	adiponectin receptor 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1317350	Adipor2	adiponectin receptor 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0002687	oligozoospermia		IEA		N	RGD:5509061	20111116	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1317350	Adipor2	adiponectin receptor 2	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0004929	decreased epididymis weight		IEA		N	RGD:5509061	20111116	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20160414	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0009303	decreased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1317350	Adipor2	adiponectin receptor 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0011019	abnormal adaptive thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:24531262
1317350	Adipor2	adiponectin receptor 2	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:24531262
1317350	Adipor2	adiponectin receptor 2	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0020550	multinucleated giant male germ cells		IEA		N	RGD:5509061	20180301	MGI			
1317350	Adipor2	adiponectin receptor 2	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:17068142
1317350	Adipor2	adiponectin receptor 2	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:17327425
1317350	Adipor2	adiponectin receptor 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:17327425
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:16810330
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20160218	MGI			PMID:16810330
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20160218	MGI			PMID:16810330
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20181227	MGI			
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20221215	MGI			
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20160218	MGI			PMID:16810330
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0006205	embryonic lethality between implantation and somite formation		IEA		N	RGD:5509061	20141003	MGI			
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:16810330
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:16810330
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0011191	increased embryonic epiblast cell apoptosis		IAGP		N	RGD:5509061	20160218	MGI			PMID:16810330
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0011192	decreased embryonic epiblast cell proliferation		IAGP		N	RGD:5509061	20160218	MGI			PMID:16810330
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1317356	Wee1	WEE 1 homolog 1 (S. pombe)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20190314	MGI			PMID:30042348
1317357	Clptm1l	CLPTM1-like	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20190314	MGI			PMID:30042348
1317357	Clptm1l	CLPTM1-like	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20181227	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1317357	Clptm1l	CLPTM1-like	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190314	MGI			PMID:30042348
1317357	Clptm1l	CLPTM1-like	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190314	MGI			PMID:30042348
1317361	Serpina1f	serine (or cysteine) peptidase inhibitor, clade A, member 1F	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1317361	Serpina1f	serine (or cysteine) peptidase inhibitor, clade A, member 1F	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004338	small clavicle		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0010926	increased osteoid volume		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0010969	absent compact bone		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150122	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0011585	decreased alkaline phosphatase activity		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0011585	decreased alkaline phosphatase activity		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20180906	MGI			PMID:28880886
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20180906	MGI			PMID:29174564
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0030275	thin frontal bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:20838829
1317362	Ifitm5	interferon induced transmembrane protein 5	gene	MP:0030850	abnormal ilium body morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:20838829
1317367	Stxbp4	syntaxin binding protein 4	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1317367	Stxbp4	syntaxin binding protein 4	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1317370	Kntc1	kinetochore associated 1	gene	MP:0000585	kinked tail		IEA		N	RGD:5509061	20150730	MGI			
1317370	Kntc1	kinetochore associated 1	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20201231	MGI			
1317370	Kntc1	kinetochore associated 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317370	Kntc1	kinetochore associated 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1317372	Tmem87b	transmembrane protein 87B	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20240523	MGI			
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20240307	MGI			PMID:37275850
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20240307	MGI			PMID:37275850
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:37275850
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20240307	MGI			PMID:37275850
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210520	MGI			
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20240523	MGI			
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20221215	MGI			
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240307	MGI			PMID:37275850
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0011243	decreased fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20240307	MGI			PMID:37275850
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:37275850
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0012121	sclerocornea		IEA		N	RGD:5509061	20240523	MGI			
1317374	Ing5	inhibitor of growth family, member 5	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1317377	Pcbp4	poly(rC) binding protein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20171207	MGI			PMID:26915821
1317377	Pcbp4	poly(rC) binding protein 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20171207	MGI			PMID:26915821
1317377	Pcbp4	poly(rC) binding protein 4	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20171207	MGI			PMID:26915821
1317377	Pcbp4	poly(rC) binding protein 4	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20171207	MGI			PMID:26915821
1317377	Pcbp4	poly(rC) binding protein 4	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20171207	MGI			PMID:26915821
1317377	Pcbp4	poly(rC) binding protein 4	gene	MP:0010294	increased kidney tumor incidence		IAGP		N	RGD:5509061	20171207	MGI			PMID:26915821
1317377	Pcbp4	poly(rC) binding protein 4	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20171207	MGI			PMID:26915821
1317379	Wbp11	WW domain binding protein 11	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0000467	abnormal esophagus morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0004600	abnormal vertebral transverse process morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0008832	hemivertebra		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0008922	abnormal cervical rib		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0008970	choanal atresia		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0011854	cerebral edema		IAGP		N	RGD:5509061	20210325	MGI			PMID:33276377
1317379	Wbp11	WW domain binding protein 11	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:33276377
1317381	Phc2	polyhomeotic 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1317381	Phc2	polyhomeotic 2	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0000080	abnormal exoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24091011
1317381	Phc2	polyhomeotic 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215307
1317381	Phc2	polyhomeotic 2	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24091011
1317381	Phc2	polyhomeotic 2	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1317381	Phc2	polyhomeotic 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24091011
1317381	Phc2	polyhomeotic 2	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1317381	Phc2	polyhomeotic 2	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24091011
1317381	Phc2	polyhomeotic 2	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1317381	Phc2	polyhomeotic 2	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24091011
1317381	Phc2	polyhomeotic 2	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24091011
1317381	Phc2	polyhomeotic 2	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1317381	Phc2	polyhomeotic 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1317381	Phc2	polyhomeotic 2	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0010702	split cervical atlas		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0010703	split cervical axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1317381	Phc2	polyhomeotic 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317381	Phc2	polyhomeotic 2	gene	MP:0012062	small tail bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1317383	Ints15	integrator complex subunit 15	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0001785	edema		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0005098	abnormal optic choroid morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0006182	increased retina hemangioma incidence		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20260402	MGI			
1317383	Ints15	integrator complex subunit 15	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317383	Ints15	integrator complex subunit 15	gene	MP:0031428	lens dislocation		IAGP		N	RGD:5509061	20240523	MGI			PMID:36851842
1317385	Ptdss2	phosphatidylserine synthase 2	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361952
1317385	Ptdss2	phosphatidylserine synthase 2	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361952
1317385	Ptdss2	phosphatidylserine synthase 2	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361952
1317385	Ptdss2	phosphatidylserine synthase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361952
1317385	Ptdss2	phosphatidylserine synthase 2	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361952
1317385	Ptdss2	phosphatidylserine synthase 2	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18343815
1317385	Ptdss2	phosphatidylserine synthase 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361952
1317385	Ptdss2	phosphatidylserine synthase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18343815
1317386	Ammecr1l	AMME chromosomal region gene 1-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1317389	Mmp1a	matrix metallopeptidase 1a (interstitial collagenase)	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23548910
1317389	Mmp1a	matrix metallopeptidase 1a (interstitial collagenase)	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23548910
1317389	Mmp1a	matrix metallopeptidase 1a (interstitial collagenase)	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23548910
1317389	Mmp1a	matrix metallopeptidase 1a (interstitial collagenase)	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23548910
1317389	Mmp1a	matrix metallopeptidase 1a (interstitial collagenase)	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23548910
1317389	Mmp1a	matrix metallopeptidase 1a (interstitial collagenase)	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23548910
1317389	Mmp1a	matrix metallopeptidase 1a (interstitial collagenase)	gene	MP:0008654	increased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23548910
1317389	Mmp1a	matrix metallopeptidase 1a (interstitial collagenase)	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23548910
1317389	Mmp1a	matrix metallopeptidase 1a (interstitial collagenase)	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23548910
1317392	Mfap5	microfibrillar associated protein 5	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1317392	Mfap5	microfibrillar associated protein 5	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1317392	Mfap5	microfibrillar associated protein 5	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1317392	Mfap5	microfibrillar associated protein 5	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1317392	Mfap5	microfibrillar associated protein 5	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1317392	Mfap5	microfibrillar associated protein 5	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1317392	Mfap5	microfibrillar associated protein 5	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1317392	Mfap5	microfibrillar associated protein 5	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1317392	Mfap5	microfibrillar associated protein 5	gene	MP:0010963	abnormal compact bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23963447
1317394	Tbc1d15	TBC1 domain family, member 15	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20240620	MGI			PMID:35680100
1317394	Tbc1d15	TBC1 domain family, member 15	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20240620	MGI			PMID:35680100
1317394	Tbc1d15	TBC1 domain family, member 15	gene	MP:0014239	abnormal intracellular organelle morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:35680100
1317394	Tbc1d15	TBC1 domain family, member 15	gene	MP:0031217	increased susceptibility to myocardial ischemic injury		IAGP		N	RGD:5509061	20240620	MGI			PMID:35680100
1317396	Ldb2	LIM domain binding 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1317398	Tmem9	transmembrane protein 9	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20211125	MGI			PMID:30374053
1317398	Tmem9	transmembrane protein 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:30374053
1317398	Tmem9	transmembrane protein 9	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20211125	MGI			PMID:30374053
1317398	Tmem9	transmembrane protein 9	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20211125	MGI			PMID:30374053
1317398	Tmem9	transmembrane protein 9	gene	MP:0012434	decreased intestinal adenoma incidence		IAGP		N	RGD:5509061	20211125	MGI			PMID:30374053
1317398	Tmem9	transmembrane protein 9	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:30374053
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210826	MGI			
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20230302	MGI			PMID:34161347
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210826	MGI			
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0004781	abnormal surfactant composition		IAGP		N	RGD:5509061	20230302	MGI			PMID:34161347
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20230302	MGI			PMID:34161347
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20230302	MGI			PMID:34161347
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20230302	MGI			PMID:34161347
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0010935	increased airway resistance		IAGP		N	RGD:5509061	20230302	MGI			PMID:34161347
1317408	Lamp3	lysosomal-associated membrane protein 3	gene	MP:0010992	increased surfactant secretion		IAGP		N	RGD:5509061	20230302	MGI			PMID:34161347
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20251204	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20240523	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20230601	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20251204	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251204	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251204	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20251204	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20241121	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251204	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251204	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251204	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0012099	decreased spongiotrophoblast size		IEA		N	RGD:5509061	20251204	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230601	MGI			
1317409	Bltp2	bridge-like lipid transfer protein family member 2	gene	MP:0014134	abnormal embryo morphology		IEA		N	RGD:5509061	20251204	MGI			
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0004962	decreased prostate gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317410	Paip2b	poly(A) binding protein interacting protein 2B	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739757
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20230119	MGI			
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230119	MGI			
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0006045	mitral valve regurgitation		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20096683
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317412	Pcnt	pericentrin (kendrin)	gene	MP:0012285	misaligned sternebrae		IAGP		N	RGD:5509061	20160211	MGI			PMID:25220058
1317414	Cldn4	claudin 4	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0000535	ureter urothelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150129	MGI			PMID:25106430
1317414	Cldn4	claudin 4	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0003016	increased circulating bicarbonate level		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0003028	alkalosis		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0003589	abnormal ureter physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0010109	abnormal renal sodium reabsorption		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317414	Cldn4	claudin 4	gene	MP:0010111	abnormal renal calcium reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0011336	abnormal kidney pelvis urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23284964
1317414	Cldn4	claudin 4	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20150122	MGI			PMID:25157135
1317418	R3hcc1l	R3H domain and coiled-coil containing 1 like	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20181227	MGI			
1317418	R3hcc1l	R3H domain and coiled-coil containing 1 like	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1317418	R3hcc1l	R3H domain and coiled-coil containing 1 like	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923606
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0010017	visceral vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0010020	spleen vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15798182
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923606
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923606
1317424	Morf4l1	mortality factor 4 like 1	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:15798182
1317428	Cemip2	cell migration inducing hyaluronidase 2	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:34624311
1317428	Cemip2	cell migration inducing hyaluronidase 2	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:34624311
1317428	Cemip2	cell migration inducing hyaluronidase 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:34624311
1317428	Cemip2	cell migration inducing hyaluronidase 2	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:34624311
1317428	Cemip2	cell migration inducing hyaluronidase 2	gene	MP:0002827	abnormal renal corpuscle morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:34624311
1317428	Cemip2	cell migration inducing hyaluronidase 2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20240404	MGI			PMID:34624311
1317428	Cemip2	cell migration inducing hyaluronidase 2	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:34624311
1317428	Cemip2	cell migration inducing hyaluronidase 2	gene	MP:0014427	increased circulating hyaluronic acid level		IAGP		N	RGD:5509061	20240425	MGI			PMID:34624311
1317428	Cemip2	cell migration inducing hyaluronidase 2	gene	MP:0014429	increased hyaluronic acid level		IAGP		N	RGD:5509061	20240425	MGI			PMID:34624311
1317430	Mrpl58	mitochondrial ribosomal protein L58	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1317430	Mrpl58	mitochondrial ribosomal protein L58	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1317430	Mrpl58	mitochondrial ribosomal protein L58	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1317430	Mrpl58	mitochondrial ribosomal protein L58	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1317430	Mrpl58	mitochondrial ribosomal protein L58	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0000256	echinocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317433	Ppp1r15b	protein phosphatase 1, regulatory subunit 15B	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19181853
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317435	Def6	differentially expressed in FDCP 6	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470246
1317437	Ca14	carbonic anhydrase 14	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260723
1317437	Ca14	carbonic anhydrase 14	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260723
1317437	Ca14	carbonic anhydrase 14	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260723
1317437	Ca14	carbonic anhydrase 14	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260723
1317437	Ca14	carbonic anhydrase 14	gene	MP:0004043	abnormal pH regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260723
1317442	Usp30	ubiquitin specific peptidase 30	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
1317442	Usp30	ubiquitin specific peptidase 30	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1317442	Usp30	ubiquitin specific peptidase 30	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210520	MGI			
1317442	Usp30	ubiquitin specific peptidase 30	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20200423	MGI			PMID:32142684
1317442	Usp30	ubiquitin specific peptidase 30	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20200423	MGI			PMID:32142684
1317444	Glrx2	glutaredoxin 2	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21983434
1317444	Glrx2	glutaredoxin 2	gene	MP:0014967	increased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:21983434
1317449	Prr5	proline rich 5 (renal)	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1317449	Prr5	proline rich 5 (renal)	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1317449	Prr5	proline rich 5 (renal)	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1317449	Prr5	proline rich 5 (renal)	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1317454	Actr5	ARP5 actin-related protein 5	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1317454	Actr5	ARP5 actin-related protein 5	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1317454	Actr5	ARP5 actin-related protein 5	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1317454	Actr5	ARP5 actin-related protein 5	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20181227	MGI			
1317454	Actr5	ARP5 actin-related protein 5	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20181227	MGI			
1317454	Actr5	ARP5 actin-related protein 5	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1317454	Actr5	ARP5 actin-related protein 5	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20181227	MGI			
1317454	Actr5	ARP5 actin-related protein 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317454	Actr5	ARP5 actin-related protein 5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1317457	Ube2l6	ubiquitin-conjugating enzyme E2L 6	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1317457	Ube2l6	ubiquitin-conjugating enzyme E2L 6	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20260402	MGI			
1317462	Slc31a2	solute carrier family 31, member 2	gene	MP:0010243	increased kidney copper level		IAGP		N	RGD:5509061	20250220	MGI			PMID:24167251
1317462	Slc31a2	solute carrier family 31, member 2	gene	MP:0011214	increased brain copper level		IAGP		N	RGD:5509061	20250220	MGI			PMID:24167251
1317462	Slc31a2	solute carrier family 31, member 2	gene	MP:0014539	increased copper level		IAGP		N	RGD:5509061	20250220	MGI			PMID:24167251
1317465	Ppa2	pyrophosphatase (inorganic) 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1317465	Ppa2	pyrophosphatase (inorganic) 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210520	MGI			
1317466	Fam171a2	family with sequence similarity 171, member A2	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1317466	Fam171a2	family with sequence similarity 171, member A2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1317466	Fam171a2	family with sequence similarity 171, member A2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20250515	MGI			PMID:39977508
1317466	Fam171a2	family with sequence similarity 171, member A2	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20250515	MGI			PMID:39977508
1317466	Fam171a2	family with sequence similarity 171, member A2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1317466	Fam171a2	family with sequence similarity 171, member A2	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:39977508
1317468	Phyhipl	phytanoyl-CoA hydroxylase interacting protein-like	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20240314	MGI			PMID:33712038
1317468	Phyhipl	phytanoyl-CoA hydroxylase interacting protein-like	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20240314	MGI			PMID:33712038
1317468	Phyhipl	phytanoyl-CoA hydroxylase interacting protein-like	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20240314	MGI			PMID:33712038
1317468	Phyhipl	phytanoyl-CoA hydroxylase interacting protein-like	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20240314	MGI			PMID:33712038
1317468	Phyhipl	phytanoyl-CoA hydroxylase interacting protein-like	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20240314	MGI			PMID:33712038
1317468	Phyhipl	phytanoyl-CoA hydroxylase interacting protein-like	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20240314	MGI			PMID:33712038
1317468	Phyhipl	phytanoyl-CoA hydroxylase interacting protein-like	gene	MP:0003894	abnormal Purkinje cell innervation		IAGP		N	RGD:5509061	20240314	MGI			PMID:33712038
1317468	Phyhipl	phytanoyl-CoA hydroxylase interacting protein-like	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20240314	MGI			PMID:33712038
1317468	Phyhipl	phytanoyl-CoA hydroxylase interacting protein-like	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240314	MGI			PMID:33712038
1317471	Sync	syncoilin	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367591
1317471	Sync	syncoilin	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594912
1317471	Sync	syncoilin	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594912
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927621
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601352
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927621
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927621
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601352
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927621
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927621
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550846
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601352
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869507
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:10601352
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:11927621
1317473	Selplg	selectin, platelet (p-selectin) ligand	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:18550846
1317475	Rilpl1	Rab interacting lysosomal protein-like 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1317475	Rilpl1	Rab interacting lysosomal protein-like 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1317477	Pkd1l3	polycystic kidney disease 1 like 3	gene	MP:0001985	abnormal gustatory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625513
1317477	Pkd1l3	polycystic kidney disease 1 like 3	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21625513
1317479	Rrp36	ribosomal RNA processing 36	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1317479	Rrp36	ribosomal RNA processing 36	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1317487	Luc7l3	LUC7-like 3 (S. cerevisiae)	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1317487	Luc7l3	LUC7-like 3 (S. cerevisiae)	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1317487	Luc7l3	LUC7-like 3 (S. cerevisiae)	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1317487	Luc7l3	LUC7-like 3 (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1317487	Luc7l3	LUC7-like 3 (S. cerevisiae)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1317488	Ola1	Obg-like ATPase 1	gene	MP:0000597	delayed hepatic development		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1317488	Ola1	Obg-like ATPase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20201022	MGI			
1317488	Ola1	Obg-like ATPase 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170608	MGI			PMID:27481995
1317488	Ola1	Obg-like ATPase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20160804	MGI			
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691904
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0005298	abnormal clavicle morphology		IEA		N	RGD:5509061	20160804	MGI			
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691904
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691904
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691904
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691904
1317495	Pnpt1	polyribonucleotide nucleotidyltransferase 1	gene	MP:0014910	decreased hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:20691904
1317497	Hacl2	2-hydroxyacyl-CoA lyase 2	gene	MP:0003075	abnormal response to CNS ischemic injury		IAGP		N	RGD:5509061	20241226	MGI			PMID:38987239
1317497	Hacl2	2-hydroxyacyl-CoA lyase 2	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20241226	MGI			PMID:38987239
1317497	Hacl2	2-hydroxyacyl-CoA lyase 2	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:38987239
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20190418	MGI			PMID:27528230
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190418	MGI			PMID:27528230
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0001923	reduced female fertility		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0002680	decreased corpora lutea number		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0002687	oligozoospermia		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0004901	decreased male germ cell number		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27528230
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0006380	abnormal spermatid morphology		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20190418	MGI			PMID:27528230
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27528230
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20190418	MGI			PMID:27528230
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0013159	Purkinje cell axonal dystrophy		IAGP		N	RGD:5509061	20190418	MGI			PMID:27528230
1317499	Herc2	HECT and RLD domain containing E3 ubiquitin protein ligase 2	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1317501	Cytip	cytohesin 1 interacting protein	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809763
1317501	Cytip	cytohesin 1 interacting protein	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809763
1317501	Cytip	cytohesin 1 interacting protein	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809763
1317501	Cytip	cytohesin 1 interacting protein	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809763
1317501	Cytip	cytohesin 1 interacting protein	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809763
1317501	Cytip	cytohesin 1 interacting protein	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914744
1317501	Cytip	cytohesin 1 interacting protein	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809763
1317501	Cytip	cytohesin 1 interacting protein	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809763
1317503	Sh2d4a	SH2 domain containing 4A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641339
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191128	MGI			
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1317512	Mrps18c	mitochondrial ribosomal protein S18C	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260716	MGI			PMID:32376682
1317515	Plagl2	pleiomorphic adenoma gene-like 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983586
1317515	Plagl2	pleiomorphic adenoma gene-like 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983586
1317515	Plagl2	pleiomorphic adenoma gene-like 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983586
1317515	Plagl2	pleiomorphic adenoma gene-like 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983586
1317515	Plagl2	pleiomorphic adenoma gene-like 2	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983586
1317515	Plagl2	pleiomorphic adenoma gene-like 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983586
1317515	Plagl2	pleiomorphic adenoma gene-like 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983586
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20181227	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20181227	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000458	abnormal mandible morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000552	abnormal radius morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0001340	abnormal eyelid morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20181227	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0002187	abnormal fibula morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0004692	small pubis		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20181227	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0005108	abnormal ulna morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0005270	abnormal zygomatic bone morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0005298	abnormal clavicle morphology		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20210128	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0012072	decreased susceptibility to osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526378
1317517	Lrrk1	leucine-rich repeat kinase 1	gene	MP:0030610	absent teeth		IEA		N	RGD:5509061	20180726	MGI			
1317519	Med16	mediator complex subunit 16	gene	MP:0000603	pale liver		IEA		N	RGD:5509061	20210520	MGI			
1317519	Med16	mediator complex subunit 16	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170504	MGI			
1317519	Med16	mediator complex subunit 16	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1317519	Med16	mediator complex subunit 16	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1317519	Med16	mediator complex subunit 16	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20170504	MGI			
1317519	Med16	mediator complex subunit 16	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20260402	MGI			PMID:40081376
1317519	Med16	mediator complex subunit 16	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20260402	MGI			PMID:40081376
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20702777
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20702777
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20702777
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20702777
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0008861	abnormal hair shedding		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20702777
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20702777
1317523	Farp2	FERM, RhoGEF and pleckstrin domain protein 2	gene	MP:0010877	abnormal trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20702777
1317525	Shpk	sedoheptulokinase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20240822	MGI			PMID:34823997
1317525	Shpk	sedoheptulokinase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20240822	MGI			PMID:34823997
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0003223	decreased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0008402	increased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0008800	increased small intestinal crypt cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0010156	abnormal small intestinal crypt cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23726973
1317527	Tigar	Trp53 induced glycolysis regulatory phosphatase	gene	MP:0011638	abnormal mitochondrial chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22044588
1317529	Ccr1l1	C-C motif chemokine receptor 1 like 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1317529	Ccr1l1	C-C motif chemokine receptor 1 like 1	gene	MP:0005387	immune system phenotype		IAGP		N	RGD:5509061	20210617	MGI			PMID:33548230
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20160421	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0003173	decreased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20181227	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20160811	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20160421	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317533	Plekhm1	pleckstrin homology and RUN domain containing M1	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20170518	MGI			PMID:27777970
1317535	Efhc1	EF-hand domain (C-terminal) containing 1	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147686
1317535	Efhc1	EF-hand domain (C-terminal) containing 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147686
1317535	Efhc1	EF-hand domain (C-terminal) containing 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147686
1317535	Efhc1	EF-hand domain (C-terminal) containing 1	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147686
1317535	Efhc1	EF-hand domain (C-terminal) containing 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147686
1317536	Dennd6b	DENN domain containing 6B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1317536	Dennd6b	DENN domain containing 6B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1317536	Dennd6b	DENN domain containing 6B	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20230119	MGI			
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16291793
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024028
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0002251	abnormal nasopharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0003760	decreased palatal length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16291793
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024028
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0010994	aerophagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12203729
1317541	Sim2	single-minded family bHLH transcription factor 2	gene	MP:0014429	increased hyaluronic acid level		IAGP		N	RGD:5509061	20240425	MGI			PMID:12203729
1317543	Rbm7	RNA binding motif protein 7	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:32187520
1317543	Rbm7	RNA binding motif protein 7	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:32187520
1317543	Rbm7	RNA binding motif protein 7	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:32187520
1317543	Rbm7	RNA binding motif protein 7	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20201001	MGI			PMID:32187520
1317543	Rbm7	RNA binding motif protein 7	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:32187520
1317545	Ccnk	cyclin K	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22012619
1317549	Cpne5	copine V	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20160811	MGI			
1317549	Cpne5	copine V	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20230126	MGI			PMID:28168849
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0004971	dermal hyperplasia		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0009794	sebaceous gland hyperplasia		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20250424	MGI			PMID:29190822
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1317551	Ppp2r5a	protein phosphatase 2, regulatory subunit B', alpha	gene	MP:0012110	increased hair follicle number		IAGP		N	RGD:5509061	20181004	MGI			PMID:29190822
1317552	Ralgapa2	Ral GTPase activating protein, alpha subunit 2 (catalytic)	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20260402	MGI			
1317552	Ralgapa2	Ral GTPase activating protein, alpha subunit 2 (catalytic)	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20260402	MGI			
1317552	Ralgapa2	Ral GTPase activating protein, alpha subunit 2 (catalytic)	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20260402	MGI			
1317552	Ralgapa2	Ral GTPase activating protein, alpha subunit 2 (catalytic)	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22450745
1317552	Ralgapa2	Ral GTPase activating protein, alpha subunit 2 (catalytic)	gene	MP:0005544	cornea deposits		IEA		N	RGD:5509061	20260402	MGI			
1317552	Ralgapa2	Ral GTPase activating protein, alpha subunit 2 (catalytic)	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20260402	MGI			
1317552	Ralgapa2	Ral GTPase activating protein, alpha subunit 2 (catalytic)	gene	MP:0010289	increased urinary system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22450745
1317552	Ralgapa2	Ral GTPase activating protein, alpha subunit 2 (catalytic)	gene	MP:0011897	decreased circulating unsaturated transferrin level		IEA		N	RGD:5509061	20260402	MGI			
1317556	Slc35g3	solute carrier family 35, member G3	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20260507	MGI			PMID:41222000
1317556	Slc35g3	solute carrier family 35, member G3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260507	MGI			PMID:41222000
1317556	Slc35g3	solute carrier family 35, member G3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:41222000
1317556	Slc35g3	solute carrier family 35, member G3	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20260507	MGI			PMID:41222000
1317556	Slc35g3	solute carrier family 35, member G3	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20260507	MGI			PMID:41222000
1317556	Slc35g3	solute carrier family 35, member G3	gene	MP:0031010	failure of sperm-egg fusion		IAGP		N	RGD:5509061	20260507	MGI			PMID:41222000
1317556	Slc35g3	solute carrier family 35, member G3	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20260507	MGI			PMID:41222000
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20240523	MGI			
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20240523	MGI			
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20231123	MGI			PMID:37891173
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0013507	increased ovary apoptosis		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1317557	Swsap1	SWIM type zinc finger 7 associated protein 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20240523	MGI			
1317559	Cldn10	claudin 10	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0002986	decreased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0006357	abnormal circulating mineral level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0010092	increased circulating magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0010111	abnormal renal calcium reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1317559	Cldn10	claudin 10	gene	MP:0011436	decreased urine magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317559	Cldn10	claudin 10	gene	MP:0011467	decreased urine urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22891322
1317561	Pdgfrl	platelet-derived growth factor receptor-like	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1317561	Pdgfrl	platelet-derived growth factor receptor-like	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1317563	Eif5a	eukaryotic translation initiation factor 5A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200521	MGI			PMID:21850436
1317563	Eif5a	eukaryotic translation initiation factor 5A	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20200521	MGI			PMID:21850436
1317563	Eif5a	eukaryotic translation initiation factor 5A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200521	MGI			PMID:21850436
1317564	Glis1	GLIS family zinc finger 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12385751
1317564	Glis1	GLIS family zinc finger 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12385751
1317564	Glis1	GLIS family zinc finger 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12385751
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0014632	increased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0014635	increased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0014637	increased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:38236177
1317565	Ccdc159	coiled-coil domain containing 159	gene	MP:0030591	absent sperm fibrous sheath		IAGP		N	RGD:5509061	20240808	MGI			PMID:38236177
1317570	Ankrd6	ankyrin repeat domain 6	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20150924	MGI			PMID:25218921
1317570	Ankrd6	ankyrin repeat domain 6	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20150924	MGI			PMID:25218921
1317570	Ankrd6	ankyrin repeat domain 6	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25218921
1317570	Ankrd6	ankyrin repeat domain 6	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25218921
1317570	Ankrd6	ankyrin repeat domain 6	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25218921
1317572	Rnf8	ring finger protein 8	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385750
1317572	Rnf8	ring finger protein 8	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250220	MGI			PMID:20385750
1317574	Setd1b	SET domain containing 1B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550110
1317574	Setd1b	SET domain containing 1B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550110
1317576	Vps11	VPS11, CORVET/HOPS core subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20260402	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20180215	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0002491	decreased IgD level		IEA		N	RGD:5509061	20180215	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0003393	decreased cardiac output		IEA		N	RGD:5509061	20260402	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20260402	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23333305
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20170615	MGI			PMID:26774285
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368578
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20170615	MGI			PMID:26774285
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20210826	MGI			PMID:33857404
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20180215	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0005380	embryo phenotype		IAGP		N	RGD:5509061	20250918	MGI			PMID:38407237
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20260402	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23333305
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0008409	increased cellular sensitivity to hydroxyurea induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578828
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20210826	MGI			PMID:33857404
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20170615	MGI			PMID:26774285
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0011952	decreased cardiac stroke volume		IEA		N	RGD:5509061	20260402	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640136
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1317578	Trp53bp1	transformation related protein 53 binding protein 1	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20180215	MGI			
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10624948
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11511537
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17828260
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0000860	abnormal primary somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17828260
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0000862	absent barrels in primary somatosensory cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10624948
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271116
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147377
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147377
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001437	no swallowing reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271116
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10624948
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17828260
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271116
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17828260
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004167	abnormal cingulate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147377
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004330	abnormal vestibular saccular macula morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004407	increased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004589	abnormal cochlear hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0004840	increased Deiters cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147377
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147377
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0008221	abnormal hippocampal commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0008304	abnormal organ of Corti supporting cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0008307	short scala media		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914494
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0008307	short scala media		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271116
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021036
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0011389	absent optic disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147377
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0012293	impaired active avoidance behavior		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0012312	impaired avoidance learning behavior		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0012318	slow extinction of fear memory		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0012535	abnormal optic fissure closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147377
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0013911	fused vestibular saccule and utricle		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0020068	increased neocortex volume		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0020083	decreased hippocampus volume		IAGP		N	RGD:5509061	20220127	MGI			PMID:31600777
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317579	Nr2f1	nuclear receptor subfamily 2, group F, member 1	gene	MP:0021110	increased social investigation		IAGP		N	RGD:5509061	20251030	MGI			PMID:40855817
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713653
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079967
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589175
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713653
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589175
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589175
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589175
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0008647	increased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589175
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589175
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15589175
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713653
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:15589175
1317581	Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	gene	MP:0031025	decreased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:15589175
1317584	Bms1	BMS1, ribosome biogenesis factor	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1317584	Bms1	BMS1, ribosome biogenesis factor	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1317584	Bms1	BMS1, ribosome biogenesis factor	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1317584	Bms1	BMS1, ribosome biogenesis factor	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20181227	MGI			
1317584	Bms1	BMS1, ribosome biogenesis factor	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1317584	Bms1	BMS1, ribosome biogenesis factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865699
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0001070	abnormal abducens nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865699
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865699
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865699
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913017
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0002329	abnormal blood gas level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913017
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0003972	decreased pituitary hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0005134	decreased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0008320	absent adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0008335	decreased gonadotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0008336	absent gonadotrophs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913017
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913017
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913017
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9865699
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0013349	small Rathke's pouch		IAGP		N	RGD:5509061	20141218	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0013351	abnormal Rathke's pouch development		IAGP		N	RGD:5509061	20141218	MGI			PMID:12183375
1317586	Lhx4	LIM homeobox protein 4	gene	MP:0013352	abnormal Rathke's pouch apoptosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:12183375
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0000565	oligodactyly		IEA		N	RGD:5509061	20160804	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0001807	decreased IgA level		IEA		N	RGD:5509061	20160804	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20160804	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20160804	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1317588	Usp12	ubiquitin specific peptidase 12	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20160804	MGI			
1317590	Dnajc13	DnaJ heat shock protein family (Hsp40) member C13	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20260402	MGI			
1317590	Dnajc13	DnaJ heat shock protein family (Hsp40) member C13	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200507	MGI			PMID:31082451
1317590	Dnajc13	DnaJ heat shock protein family (Hsp40) member C13	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1317590	Dnajc13	DnaJ heat shock protein family (Hsp40) member C13	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20260402	MGI			
1317590	Dnajc13	DnaJ heat shock protein family (Hsp40) member C13	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1317590	Dnajc13	DnaJ heat shock protein family (Hsp40) member C13	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1317590	Dnajc13	DnaJ heat shock protein family (Hsp40) member C13	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1317590	Dnajc13	DnaJ heat shock protein family (Hsp40) member C13	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1317591	Gsx2	GS homeobox 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1317591	Gsx2	GS homeobox 2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1317591	Gsx2	GS homeobox 2	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208224
1317591	Gsx2	GS homeobox 2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1317591	Gsx2	GS homeobox 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1317591	Gsx2	GS homeobox 2	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1317591	Gsx2	GS homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208224
1317591	Gsx2	GS homeobox 2	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208224
1317591	Gsx2	GS homeobox 2	gene	MP:0004103	abnormal ventral striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731457
1317591	Gsx2	GS homeobox 2	gene	MP:0004186	abnormal area postrema morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208224
1317591	Gsx2	GS homeobox 2	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1317591	Gsx2	GS homeobox 2	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208224
1317591	Gsx2	GS homeobox 2	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19208224
1317591	Gsx2	GS homeobox 2	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1317591	Gsx2	GS homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398437
1317591	Gsx2	GS homeobox 2	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:11731457
1317591	Gsx2	GS homeobox 2	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:19709628
1317592	Pithd1	PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20200528	MGI			PMID:31915251
1317592	Pithd1	PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200528	MGI			PMID:31915251
1317592	Pithd1	PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200528	MGI			PMID:31915251
1317592	Pithd1	PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20200528	MGI			PMID:31915251
1317592	Pithd1	PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1	gene	MP:0005379	endocrine/exocrine gland phenotype		IAGP		N	RGD:5509061	20200528	MGI			PMID:31915251
1317592	Pithd1	PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20200528	MGI			PMID:31915251
1317592	Pithd1	PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20200528	MGI			PMID:31915251
1317592	Pithd1	PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1	gene	MP:0031408	multi-headed sperm		IAGP		N	RGD:5509061	20220630	MGI			PMID:31915251
1317595	Irf4	interferon regulatory factor 4	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1317595	Irf4	interferon regulatory factor 4	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210520	MGI			
1317595	Irf4	interferon regulatory factor 4	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210520	MGI			
1317595	Irf4	interferon regulatory factor 4	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20221215	MGI			
1317595	Irf4	interferon regulatory factor 4	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832394
1317595	Irf4	interferon regulatory factor 4	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317595	Irf4	interferon regulatory factor 4	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832394
1317595	Irf4	interferon regulatory factor 4	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832394
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767092
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832394
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12189207
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502720
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12189207
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002440	abnormal memory B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767092
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767092
1317595	Irf4	interferon regulatory factor 4	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832394
1317595	Irf4	interferon regulatory factor 4	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767092
1317595	Irf4	interferon regulatory factor 4	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21613984
1317595	Irf4	interferon regulatory factor 4	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317595	Irf4	interferon regulatory factor 4	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1317595	Irf4	interferon regulatory factor 4	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832394
1317595	Irf4	interferon regulatory factor 4	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832394
1317595	Irf4	interferon regulatory factor 4	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767092
1317595	Irf4	interferon regulatory factor 4	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832394
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12189207
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21613984
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008100	absent plasma cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767092
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008100	absent plasma cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728463
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15184678
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728463
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008217	abnormal B cell activation		IEA		N	RGD:5509061	20111116	MGI			
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767092
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767092
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008523	absent lymph node germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999800
1317595	Irf4	interferon regulatory factor 4	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20180208	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0014912	decreased fat cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:24995979
1317595	Irf4	interferon regulatory factor 4	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:8999800
1317597	Gabarapl1	GABA type A receptor associated protein like 1	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20260319	MGI			PMID:41023280
1317597	Gabarapl1	GABA type A receptor associated protein like 1	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20260319	MGI			PMID:41023280
1317601	Poll	polymerase (DNA directed), lambda	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860755
1317601	Poll	polymerase (DNA directed), lambda	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860755
1317601	Poll	polymerase (DNA directed), lambda	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860755
1317601	Poll	polymerase (DNA directed), lambda	gene	MP:0008761	abnormal immunoglobulin light chain V-J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860755
1317601	Poll	polymerase (DNA directed), lambda	gene	MP:0014762	impaired base-excision repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:15749700
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641034
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20160804	MGI			
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641034
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413922
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413922
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641034
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413922
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413922
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641034
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413922
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413922
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1317603	Nfkbid	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641034
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20201022	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20201022	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0003642	absent seminal vesicle		IEA		N	RGD:5509061	20210826	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20210520	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20210520	MGI			
1317605	Neurl4	neuralized E3 ubiquitin protein ligase 4	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11335109
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000344	absent Cajal-Retzius cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811581
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14832454
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001756	abnormal urination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14832454
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20111116	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20111116	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002632	vestigial tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029008
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002632	vestigial tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14832454
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002632	vestigial tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20141003	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11335109
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003445	sirenomelia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11335109
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003445	sirenomelia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004205	absent hyoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811581
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004459	small alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20241121	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11335109
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11335109
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11335109
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11335109
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11335109
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004648	decreased thoracic vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004656	absent sacral vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0004714	truncated notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0008031	decreased Cajal-Retzius cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0008031	decreased Cajal-Retzius cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805388
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8595882
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0008787	abnormal tailgut morphology		IEA		N	RGD:5509061	20141003	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11335109
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0012063	absent tail bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299937
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0012714	decreased ventral ectodermal ridge size		IEA		N	RGD:5509061	20141003	MGI			
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20171005	MGI			PMID:9353119
1317607	Wnt3a	wingless-type MMTV integration site family, member 3A	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:9353119
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0000265	blood vessel atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0001699	increased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317609	Vezf1	vascular endothelial zinc finger 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882861
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252746
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12620894
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252745
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252746
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0003397	increased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252746
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252746
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252746
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252746
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0009423	increased extensor digitorum longus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0009425	increased soleus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18252746
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20220519	MGI			PMID:28797108
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0010106	abnormal circulating pyruvate kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744877
1317617	Sgca	sarcoglycan, alpha (dystrophin-associated glycoprotein)	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1317619	Stard5	StAR related lipid transfer domain containing 5	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1317619	Stard5	StAR related lipid transfer domain containing 5	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1317619	Stard5	StAR related lipid transfer domain containing 5	gene	MP:0004600	abnormal vertebral transverse process morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1317620	Mpv17l2	MPV17 mitochondrial membrane protein-like 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1317620	Mpv17l2	MPV17 mitochondrial membrane protein-like 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20181227	MGI			
1317620	Mpv17l2	MPV17 mitochondrial membrane protein-like 2	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20210128	MGI			
1317620	Mpv17l2	MPV17 mitochondrial membrane protein-like 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20181227	MGI			
1317620	Mpv17l2	MPV17 mitochondrial membrane protein-like 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1317620	Mpv17l2	MPV17 mitochondrial membrane protein-like 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1317621	2610318N02Rik	RIKEN cDNA 2610318N02 gene	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20210520	MGI			
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465592
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0003228	abnormal sinus venosus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0003410	abnormal artery development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0003542	abnormal vascular endothelial cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004266	pale placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465592
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:27513872
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16037064
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0006052	cerebellum hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0006052	cerebellum hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0006339	abnormal third pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0010355	abnormal first pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0010356	abnormal second pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0010463	aorta stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16465592
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151728
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20240118	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0011514	skin hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20240118	MGI			PMID:19259391
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0012511	dilated aortic sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0030044	short forehead		IAGP		N	RGD:5509061	20170921	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0031384	impaired blood-brain barrier function		IAGP		N	RGD:5509061	20220407	MGI			PMID:21596842
1317624	Ccm2	cerebral cavernous malformation 2	gene	MP:0031593	decreased cardiac jelly amount		IAGP		N	RGD:5509061	20240229	MGI			PMID:25625206
1317626	Zfp346	zinc finger protein 346	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20220811	MGI			
1317626	Zfp346	zinc finger protein 346	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20230119	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0001714	absent trophoblast giant cells		IEA		N	RGD:5509061	20241017	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241017	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0004964	absent inner cell mass		IEA		N	RGD:5509061	20241017	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1317628	Osbp	oxysterol binding protein	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0000015	abnormal ear pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6031677
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:6031677
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6031677
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6031677
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0002963	decreased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:417081
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0002963	decreased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6232310
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0003173	decreased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739679
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0003173	decreased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:417081
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0003174	increased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:864040
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0004721	abnormal platelet dense granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2369371
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12445206
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6031677
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0005100	abnormal choroid pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11836498
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11836498
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2369371
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3516713
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1317630	Hps4	HPS4, biogenesis of lysosomal organelles complex 3 subunit 2	gene	MP:0011279	decreased ear pigmentation		IAGP		N	RGD:5509061	20170803	MGI			PMID:864040
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001401	jumpy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008509	disorganized retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008583	absent photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:22398208
1317632	Pals1	protein associated with LIN7 1, MAGUK family member	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:22398208
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230119	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20230119	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230119	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20241121	MGI			
1317634	Dhx15	DEAH-box helicase 15	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1317637	Plxna4	plexin A4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0000861	disorganized barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270798
1317637	Plxna4	plexin A4	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721238
1317637	Plxna4	plexin A4	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0001063	abnormal trochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721238
1317637	Plxna4	plexin A4	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721238
1317637	Plxna4	plexin A4	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1317637	Plxna4	plexin A4	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1317637	Plxna4	plexin A4	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296555
1317637	Plxna4	plexin A4	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721238
1317637	Plxna4	plexin A4	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270798
1317637	Plxna4	plexin A4	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20231207	MGI			
1317637	Plxna4	plexin A4	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270798
1317637	Plxna4	plexin A4	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721238
1317637	Plxna4	plexin A4	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20230119	MGI			
1317637	Plxna4	plexin A4	gene	MP:0008312	abnormal sympathetic postganglionic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270798
1317637	Plxna4	plexin A4	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296555
1317637	Plxna4	plexin A4	gene	MP:0010859	abnormal anterior commissure pars anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0010860	abnormal anterior commissure pars posterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814794
1317637	Plxna4	plexin A4	gene	MP:0014746	abnormal hippocampal mossy fiber innervation pattern		IAGP		N	RGD:5509061	20250911	MGI			PMID:17296555
1317637	Plxna4	plexin A4	gene	MP:0014746	abnormal hippocampal mossy fiber innervation pattern		IAGP		N	RGD:5509061	20250911	MGI			PMID:20484647
1317637	Plxna4	plexin A4	gene	MP:0014748	abnormal sensory neuron axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:15721238
1317638	Tekt4	tektin 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244819
1317638	Tekt4	tektin 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18951373
1317638	Tekt4	tektin 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244819
1317638	Tekt4	tektin 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244819
1317638	Tekt4	tektin 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18951373
1317638	Tekt4	tektin 4	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244819
1317638	Tekt4	tektin 4	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244819
1317638	Tekt4	tektin 4	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244819
1317638	Tekt4	tektin 4	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:17244819
1317641	Nrg3	neuregulin 3	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723730
1317641	Nrg3	neuregulin 3	gene	MP:0000629	absent mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723730
1317641	Nrg3	neuregulin 3	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20190328	MGI			PMID:27606322
1317641	Nrg3	neuregulin 3	gene	MP:0002635	reduced sensorimotor gating		IAGP		N	RGD:5509061	20190328	MGI			PMID:27606322
1317641	Nrg3	neuregulin 3	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20190328	MGI			PMID:27606322
1317641	Nrg3	neuregulin 3	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20190328	MGI			PMID:27606322
1317641	Nrg3	neuregulin 3	gene	MP:0009720	abnormal mammary gland pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723730
1317641	Nrg3	neuregulin 3	gene	MP:0009721	increased mammary gland number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723730
1317641	Nrg3	neuregulin 3	gene	MP:0009722	abnormal nipple development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723730
1317641	Nrg3	neuregulin 3	gene	MP:0009723	increased nipple number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723730
1317641	Nrg3	neuregulin 3	gene	MP:0009724	ectopic nipples		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723730
1317641	Nrg3	neuregulin 3	gene	MP:0009741	ectopic mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723730
1317643	Rad21	RAD21 cohesin complex component	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20971813
1317643	Rad21	RAD21 cohesin complex component	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832993
1317643	Rad21	RAD21 cohesin complex component	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832993
1317643	Rad21	RAD21 cohesin complex component	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832993
1317643	Rad21	RAD21 cohesin complex component	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20971813
1317643	Rad21	RAD21 cohesin complex component	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832993
1317643	Rad21	RAD21 cohesin complex component	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832993
1317643	Rad21	RAD21 cohesin complex component	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832993
1317643	Rad21	RAD21 cohesin complex component	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20971813
1317647	Papss1	3'-phosphoadenosine 5'-phosphosulfate synthase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000297	abnormal atrioventricular cushion morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0001061	abnormal oculomotor nerve morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0001092	abnormal trigeminal ganglion morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0002177	abnormal outer ear morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0002951	small thyroid gland		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0003078	aphakia		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0005262	coloboma		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20221215	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0006093	arteriovenous malformation		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0008922	abnormal cervical rib		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0009569	abnormal left lung morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0009570	abnormal right lung morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20221215	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0010259	anterior polar cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0010439	abnormal hepatic vein morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0010463	aorta stenosis		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0010484	bicuspid aortic valve		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0010713	corneal-lenticular stalk		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20160310	MGI			PMID:17179069
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013162	abnormal thyroid gland isthmus morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013163	absent thyroid gland isthmus		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013867	abnormal ventral pancreas morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013875	increased trigeminal neuroma incidence		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013913	absent costovertebral joint		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013936	abnormal thymus topology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0014003	additional anastomosis between intracranial vertebral arteries		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0014012	abnormal cranial blood vasculature morphology		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0014018	embryo tumor		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0014019	embryo cyst		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0014023	abnormal intestine placement		IEA		N	RGD:5509061	20180628	MGI			
1317653	Col4a2	collagen, type IV, alpha 2	gene	MP:0014087	retrolental blood		IEA		N	RGD:5509061	20180628	MGI			
1317657	Ap5m1	adaptor-related protein complex 5, mu 1 subunit	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1317657	Ap5m1	adaptor-related protein complex 5, mu 1 subunit	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1317657	Ap5m1	adaptor-related protein complex 5, mu 1 subunit	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1317657	Ap5m1	adaptor-related protein complex 5, mu 1 subunit	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1317657	Ap5m1	adaptor-related protein complex 5, mu 1 subunit	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1317657	Ap5m1	adaptor-related protein complex 5, mu 1 subunit	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20231207	MGI			
1317657	Ap5m1	adaptor-related protein complex 5, mu 1 subunit	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1317661	Phykpl	5-phosphohydroxy-L-lysine phospholyase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20141003	MGI			
1317661	Phykpl	5-phosphohydroxy-L-lysine phospholyase	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1317661	Phykpl	5-phosphohydroxy-L-lysine phospholyase	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20141003	MGI			
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0003442	decreased circulating glycerol level		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0010028	aciduria		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0010742	increased Schwann cell number		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0011904	abnormal Schwann cell physiology		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20181227	MGI			PMID:29661920
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0012674	tomacula		IAGP		N	RGD:5509061	20200730	MGI			PMID:32169121
1317664	Dhtkd1	dehydrogenase E1 and transketolase domain containing 1	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1317665	Arhgef40	Rho guanine nucleotide exchange factor 40	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20231207	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7655515
1317668	Btf3	basic transcription factor 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7655515
1317668	Btf3	basic transcription factor 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20230119	MGI			
1317668	Btf3	basic transcription factor 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20241121	MGI			
1317670	Cuedc2	CUE domain containing 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20191003	MGI			PMID:24882011
1317670	Cuedc2	CUE domain containing 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20191003	MGI			PMID:24882011
1317670	Cuedc2	CUE domain containing 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20191003	MGI			PMID:24882011
1317670	Cuedc2	CUE domain containing 2	gene	MP:0011078	increased macrophage cytokine production		IAGP		N	RGD:5509061	20191003	MGI			PMID:24882011
1317672	Actn2	actinin alpha 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0000486	abnormal pulmonary trunk morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0002748	abnormal pulmonary valve morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0003923	abnormal heart left atrium morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0010463	aorta stenosis		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0010605	thick pulmonary valve cusps		IAGP		N	RGD:5509061	20231221	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0014920	increased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:36899856
1317672	Actn2	actinin alpha 2	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20230601	MGI			PMID:36899856
1317674	Hapln3	hyaluronan and proteoglycan link protein 3	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20250508	MGI			
1317677	Tbcd	tubulin-specific chaperone d	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1317677	Tbcd	tubulin-specific chaperone d	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1317681	Plac8	placenta-specific 8	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404296
1317681	Plac8	placenta-specific 8	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404296
1317681	Plac8	placenta-specific 8	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:21982742
1317681	Plac8	placenta-specific 8	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1317681	Plac8	placenta-specific 8	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1317681	Plac8	placenta-specific 8	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1317681	Plac8	placenta-specific 8	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1317681	Plac8	placenta-specific 8	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20181227	MGI			
1317681	Plac8	placenta-specific 8	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404296
1317681	Plac8	placenta-specific 8	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404296
1317681	Plac8	placenta-specific 8	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1317681	Plac8	placenta-specific 8	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1317681	Plac8	placenta-specific 8	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404296
1317681	Plac8	placenta-specific 8	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20180111	MGI			PMID:21982742
1317681	Plac8	placenta-specific 8	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20180111	MGI			PMID:21982742
1317681	Plac8	placenta-specific 8	gene	MP:0009137	decreased brown fat lipid droplet number		IAGP		N	RGD:5509061	20180111	MGI			PMID:21982742
1317681	Plac8	placenta-specific 8	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
1317681	Plac8	placenta-specific 8	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:21982742
1317681	Plac8	placenta-specific 8	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20180111	MGI			PMID:21982742
1317681	Plac8	placenta-specific 8	gene	MP:0020520	whitened brown adipose tissue morphology		IAGP		N	RGD:5509061	20180208	MGI			PMID:21982742
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170105	MGI			
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317683	Usp39	ubiquitin specific peptidase 39	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16731514
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16731514
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16731514
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17056543
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107706
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940661
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107706
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940661
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:16731514
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940661
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0009131	decreased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107706
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16731514
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16731514
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940661
1317687	Ksr1	kinase suppressor of ras 1	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874031
1317692	Cabp5	calcium binding protein 5	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20210128	MGI			
1317692	Cabp5	calcium binding protein 5	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:18586882
1317692	Cabp5	calcium binding protein 5	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0010999	proteinosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20201015	MGI			PMID:31722069
1317701	Sugct	succinyl-CoA glutarate-CoA transferase	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240418	MGI			PMID:31722069
1317703	Aatk	apoptosis-associated tyrosine kinase	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573681
1317703	Aatk	apoptosis-associated tyrosine kinase	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573681
1317703	Aatk	apoptosis-associated tyrosine kinase	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573681
1317703	Aatk	apoptosis-associated tyrosine kinase	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573681
1317705	9930012K11Rik	RIKEN cDNA 9930012K11 gene	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1317705	9930012K11Rik	RIKEN cDNA 9930012K11 gene	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20230601	MGI			
1317705	9930012K11Rik	RIKEN cDNA 9930012K11 gene	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20201231	MGI			
1317705	9930012K11Rik	RIKEN cDNA 9930012K11 gene	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20211021	MGI			
1317707	Sh3bgrl3	SH3 domain binding glutamic acid-rich protein-like 3	gene	MP:0013406	abnormal epidermal immune compartment		IEA		N	RGD:5509061	20201231	MGI			
1317711	Zfp207	zinc finger protein 207	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1317711	Zfp207	zinc finger protein 207	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1317711	Zfp207	zinc finger protein 207	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1317711	Zfp207	zinc finger protein 207	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1317711	Zfp207	zinc finger protein 207	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1317711	Zfp207	zinc finger protein 207	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317713	Gna14	guanine nucleotide binding protein, alpha 14	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1317713	Gna14	guanine nucleotide binding protein, alpha 14	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20231207	MGI			
1317713	Gna14	guanine nucleotide binding protein, alpha 14	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1317713	Gna14	guanine nucleotide binding protein, alpha 14	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20250508	MGI			
1317717	Slc35f5	solute carrier family 35, member F5	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20230119	MGI			
1317723	Cggbp1	CGG triplet repeat binding protein 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210128	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210128	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20260402	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200514	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210128	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1317727	Arih1	ariadne RBR E3 ubiquitin protein ligase 1	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1317730	Fam135b	family with sequence similarity 135, member B	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220519	MGI			
1317731	Bacc1	BPTF associated chromatin complex component 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1317731	Bacc1	BPTF associated chromatin complex component 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1317731	Bacc1	BPTF associated chromatin complex component 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20250508	MGI			
1317731	Bacc1	BPTF associated chromatin complex component 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20250508	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001781	abnormal white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20161222	MGI			PMID:24358199
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20200402	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:24358199
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0003442	decreased circulating glycerol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201231	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200402	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20161222	MGI			PMID:24358199
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:24358199
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009131	decreased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009303	decreased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011156	abnormal hypodermis fat layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011169	abnormal white fat cell differentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20150430	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011941	increased fluid intake		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20161222	MGI			PMID:24358199
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:24778225
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0014911	increased fat cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0020521	browned white adipose tissue morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0030880	abnormal infrapatellar fat pad morphology		IAGP		N	RGD:5509061	20181101	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:22269949
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:23680914
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0031008	decreased bone marrow adipose tissue amount		IAGP		N	RGD:5509061	20200130	MGI			PMID:29459250
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21551454
1317733	Bscl2	BSCL2 lipid droplet biogenesis associated, seipin	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21551454
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20160811	MGI			
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20160811	MGI			
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684731
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684731
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20250424	MGI			PMID:35482924
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20250424	MGI			PMID:35482924
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0004182	abnormal spermiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684731
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684731
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684731
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20170105	MGI			
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684731
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20250424	MGI			PMID:35482924
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0008512	disorganized retina inner nuclear layer		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684731
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20170105	MGI			
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0011308	kidney corticomedullary cyst		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0011408	renal tubule hypertrophy		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20250424	MGI			PMID:35482924
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0013305	isosthenuria		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0014686	premature spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:18684731
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0020382	increased kidney epithelial cell primary cilium length		IAGP		N	RGD:5509061	20250424	MGI			PMID:35482924
1317735	Nphp1	nephronophthisis 1 (juvenile) homolog (human)	gene	MP:0031358	decreased urine output		IAGP		N	RGD:5509061	20220609	MGI			PMID:34415307
1317737	Gmnn	geminin	gene	MP:0000216	absent erythroid progenitor cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17054725
1317737	Gmnn	geminin	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20141003	MGI			
1317737	Gmnn	geminin	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20141003	MGI			
1317737	Gmnn	geminin	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847348
1317737	Gmnn	geminin	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408022
1317737	Gmnn	geminin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17054725
1317737	Gmnn	geminin	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847348
1317737	Gmnn	geminin	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17054725
1317737	Gmnn	geminin	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17054725
1317737	Gmnn	geminin	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847348
1317737	Gmnn	geminin	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847348
1317737	Gmnn	geminin	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847348
1317737	Gmnn	geminin	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847348
1317737	Gmnn	geminin	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847348
1317737	Gmnn	geminin	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17054725
1317737	Gmnn	geminin	gene	MP:0010130	decreased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847348
1317737	Gmnn	geminin	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17054725
1317737	Gmnn	geminin	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107189
1317737	Gmnn	geminin	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041951
1317737	Gmnn	geminin	gene	MP:0012102	absent trophectoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:17054725
1317738	Zpld1	zona pellucida like domain containing 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20191128	MGI			PMID:31455802
1317738	Zpld1	zona pellucida like domain containing 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20191128	MGI			PMID:31455802
1317738	Zpld1	zona pellucida like domain containing 1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20191128	MGI			PMID:31455802
1317738	Zpld1	zona pellucida like domain containing 1	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20191128	MGI			PMID:31455802
1317738	Zpld1	zona pellucida like domain containing 1	gene	MP:0004844	abnormal vestibuloocular reflex		IAGP		N	RGD:5509061	20191128	MGI			PMID:31455802
1317738	Zpld1	zona pellucida like domain containing 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1317738	Zpld1	zona pellucida like domain containing 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1317739	Ncbp3	nuclear cap binding subunit 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1317739	Ncbp3	nuclear cap binding subunit 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1317739	Ncbp3	nuclear cap binding subunit 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1317739	Ncbp3	nuclear cap binding subunit 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317744	Chst1	carbohydrate sulfotransferase 1	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254996
1317744	Chst1	carbohydrate sulfotransferase 1	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254996
1317744	Chst1	carbohydrate sulfotransferase 1	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254996
1317744	Chst1	carbohydrate sulfotransferase 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254996
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:38869368
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20250130	MGI			PMID:38869368
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0001316	cornea scarring		IAGP		N	RGD:5509061	20250130	MGI			PMID:38869368
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20181004	MGI			PMID:29590114
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:38869368
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20250130	MGI			PMID:38869368
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20250130	MGI			PMID:38869368
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20181004	MGI			PMID:29590114
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20191219	MGI			PMID:29590114
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0020854	increased cornea epithelium thickness		IAGP		N	RGD:5509061	20250130	MGI			PMID:38869368
1317745	Ppip5k2	diphosphoinositol pentakisphosphate kinase 2	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:29590114
1317747	Ergic3	ERGIC and golgi 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1317747	Ergic3	ERGIC and golgi 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1317747	Ergic3	ERGIC and golgi 3	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1317747	Ergic3	ERGIC and golgi 3	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1317747	Ergic3	ERGIC and golgi 3	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1317747	Ergic3	ERGIC and golgi 3	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1317747	Ergic3	ERGIC and golgi 3	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1317749	Phf13	PHD finger protein 13	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317749	Phf13	PHD finger protein 13	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21852425
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0031550	abnormal atrioventricular valve development		IAGP		N	RGD:5509061	20240104	MGI			PMID:20549726
1317751	Shoc2	Shoc2, leucine rich repeat scaffold protein	gene	MP:0031553	abnormal semilunar valve development		IAGP		N	RGD:5509061	20240125	MGI			PMID:20549726
1317753	AW209491	expressed sequence AW209491	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20250508	MGI			
1317753	AW209491	expressed sequence AW209491	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20250508	MGI			
1317754	Sgo1	shugoshin 1	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22262168
1317754	Sgo1	shugoshin 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160804	MGI			
1317754	Sgo1	shugoshin 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20160804	MGI			
1317754	Sgo1	shugoshin 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22262168
1317754	Sgo1	shugoshin 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22262168
1317754	Sgo1	shugoshin 1	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22262168
1317754	Sgo1	shugoshin 1	gene	MP:0004647	decreased lumbar vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1317754	Sgo1	shugoshin 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1317754	Sgo1	shugoshin 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1317754	Sgo1	shugoshin 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:22262168
1317754	Sgo1	shugoshin 1	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22262168
1317754	Sgo1	shugoshin 1	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1317754	Sgo1	shugoshin 1	gene	MP:0012436	increased colon tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22262168
1317761	Creb3l3	cAMP responsive element binding protein 3-like 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18704925
1317761	Creb3l3	cAMP responsive element binding protein 3-like 3	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18704925
1317761	Creb3l3	cAMP responsive element binding protein 3-like 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23409047
1317761	Creb3l3	cAMP responsive element binding protein 3-like 3	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23409047
1317761	Creb3l3	cAMP responsive element binding protein 3-like 3	gene	MP:0031233	decreased circulating serum amyloid protein level		IAGP		N	RGD:5509061	20210225	MGI			PMID:18704925
1317763	Xxylt1	xyloside xylosyltransferase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1317763	Xxylt1	xyloside xylosyltransferase 1	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20181227	MGI			
1317763	Xxylt1	xyloside xylosyltransferase 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1317763	Xxylt1	xyloside xylosyltransferase 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1317767	Misp	mitotic spindle positioning	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317767	Misp	mitotic spindle positioning	gene	MP:0003292	melena		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317767	Misp	mitotic spindle positioning	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317767	Misp	mitotic spindle positioning	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317767	Misp	mitotic spindle positioning	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317767	Misp	mitotic spindle positioning	gene	MP:0008838	decreased transforming growth factor beta level		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317767	Misp	mitotic spindle positioning	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317767	Misp	mitotic spindle positioning	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317767	Misp	mitotic spindle positioning	gene	MP:0014222	decreased colon goblet cell number		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317767	Misp	mitotic spindle positioning	gene	MP:0031319	impaired intestine regeneration		IAGP		N	RGD:5509061	20230622	MGI			PMID:36596561
1317769	Cul1	cullin 1	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508527
1317769	Cul1	cullin 1	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531039
1317769	Cul1	cullin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508527
1317769	Cul1	cullin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531039
1317769	Cul1	cullin 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531039
1317769	Cul1	cullin 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20150129	MGI			PMID:10508527
1317769	Cul1	cullin 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20150129	MGI			PMID:10531039
1317769	Cul1	cullin 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531039
1317769	Cul1	cullin 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508527
1317769	Cul1	cullin 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10531039
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20141003	MGI			
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0008960	abnormal axon pruning		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0014254	increased paired-pulse ratio		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0014745	abnormal hippocampal mossy fiber infrapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0020360	abnormal asymmetric synapse morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0020512	abnormal dendritic mushroom spine morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317772	Lnx1	ligand of numb-protein X 1	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20210128	MGI			
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0030980	abnormal acroplaxome morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0031374	abnormal manchette assembly		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0031387	abnormal intramanchette transport		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317774	Ccdc178	coiled coil domain containing 178	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:39157459
1317778	Cnnm2	cyclin M2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1317778	Cnnm2	cyclin M2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317778	Cnnm2	cyclin M2	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20230601	MGI			
1317778	Cnnm2	cyclin M2	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317778	Cnnm2	cyclin M2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317778	Cnnm2	cyclin M2	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20241121	MGI			
1317778	Cnnm2	cyclin M2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1317778	Cnnm2	cyclin M2	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20210429	MGI			PMID:28033128
1317778	Cnnm2	cyclin M2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20241121	MGI			
1317778	Cnnm2	cyclin M2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1317778	Cnnm2	cyclin M2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317778	Cnnm2	cyclin M2	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1317778	Cnnm2	cyclin M2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317778	Cnnm2	cyclin M2	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20210429	MGI			PMID:28033128
1317778	Cnnm2	cyclin M2	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20210429	MGI			PMID:28033128
1317778	Cnnm2	cyclin M2	gene	MP:0010093	decreased circulating magnesium level		IAGP		N	RGD:5509061	20210429	MGI			PMID:28033128
1317778	Cnnm2	cyclin M2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20210429	MGI			PMID:28033128
1317778	Cnnm2	cyclin M2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317778	Cnnm2	cyclin M2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317778	Cnnm2	cyclin M2	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317778	Cnnm2	cyclin M2	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20181227	MGI			
1317778	Cnnm2	cyclin M2	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20181227	MGI			
1317780	Golga5	golgin A5	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180503	MGI			PMID:28509431
1317780	Golga5	golgin A5	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1317780	Golga5	golgin A5	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:28509431
1317780	Golga5	golgin A5	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180503	MGI			PMID:28509431
1317780	Golga5	golgin A5	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1317780	Golga5	golgin A5	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:28509431
1317780	Golga5	golgin A5	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1317780	Golga5	golgin A5	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1317780	Golga5	golgin A5	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1317780	Golga5	golgin A5	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220519	MGI			
1317783	Msantd3	Myb/SANT-like DNA-binding domain containing 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000339	decreased enterocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697701
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718027
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718027
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393260
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697701
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697701
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000520	absent kidney		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000636	enlarged pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12907761
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828091
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718027
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718027
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718027
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718027
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393260
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028378
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22717537
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828091
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0002239	abnormal nasal septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22717537
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028378
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828091
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12907761
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20150430	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0004164	abnormal neurohypophysis morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22717537
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028378
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718027
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028378
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0008130	abnormal pituitary intermediate lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12907761
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0008366	enlarged adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12907761
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20190103	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393260
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393260
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22717537
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718027
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028378
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20150430	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010158	abnormal intestine development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393260
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010589	common truncal valve		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0010802	abnormal intestinal enteroendocrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673050
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697701
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028378
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0011513	abnormal vertebral artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013186	abnormal basilar artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20160310	MGI			PMID:22393260
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013792	abnormal small intestine goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013792	abnormal small intestine goblet cell morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:22393260
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:21383188
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013862	abnormal cecum position		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013879	duplication of ductus venosus		IEA		N	RGD:5509061	20180628	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013943	abnormal ureter topology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013945	abnormal elbow joint morphology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013977	symmetric azygos veins		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0013985	abnormal umbilical vein topology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0014076	absent Paneth cells		IAGP		N	RGD:5509061	20160310	MGI			PMID:22393260
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0014077	ectopic Paneth cells		IAGP		N	RGD:5509061	20160310	MGI			PMID:22393260
1317787	Tcf7l2	transcription factor 7 like 2, T cell specific, HMG box	gene	MP:0020485	abnormal inferior vena cava topology		IEA		N	RGD:5509061	20180628	MGI			
1317788	Rnf213	ring finger protein 213	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20251030	MGI			PMID:40485582
1317788	Rnf213	ring finger protein 213	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
1317788	Rnf213	ring finger protein 213	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20251030	MGI			PMID:40485582
1317788	Rnf213	ring finger protein 213	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20251030	MGI			PMID:40485582
1317788	Rnf213	ring finger protein 213	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160407	MGI			PMID:26315378
1317788	Rnf213	ring finger protein 213	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20251030	MGI			PMID:40485582
1317788	Rnf213	ring finger protein 213	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
1317788	Rnf213	ring finger protein 213	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
1317788	Rnf213	ring finger protein 213	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20251030	MGI			PMID:40485582
1317788	Rnf213	ring finger protein 213	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20160304	MGI			PMID:25446450
1317788	Rnf213	ring finger protein 213	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20160304	MGI			PMID:25446450
1317788	Rnf213	ring finger protein 213	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
1317788	Rnf213	ring finger protein 213	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
1317788	Rnf213	ring finger protein 213	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20251030	MGI			PMID:40485582
1317788	Rnf213	ring finger protein 213	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
1317788	Rnf213	ring finger protein 213	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
1317788	Rnf213	ring finger protein 213	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
1317788	Rnf213	ring finger protein 213	gene	MP:0010911	abnormal pulmonary acinus morphology		IAGP		N	RGD:5509061	20251030	MGI			PMID:40485582
1317788	Rnf213	ring finger protein 213	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20251030	MGI			PMID:40485582
1317788	Rnf213	ring finger protein 213	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410753
1317788	Rnf213	ring finger protein 213	gene	MP:0014473	increased pulmonary alveolus wall thickness		IAGP		N	RGD:5509061	20251030	MGI			PMID:40485582
1317794	Ogn	osteoglycin	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1317794	Ogn	osteoglycin	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432342
1317794	Ogn	osteoglycin	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1317794	Ogn	osteoglycin	gene	MP:0003966	abnormal adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21664248
1317794	Ogn	osteoglycin	gene	MP:0005275	abnormal skin tensile strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432342
1317794	Ogn	osteoglycin	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432342
1317794	Ogn	osteoglycin	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1317794	Ogn	osteoglycin	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056351
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056351
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056351
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056351
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056351
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056351
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0008031	decreased Cajal-Retzius cell number		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0008440	abnormal subplate morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056351
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317797	Dmrta2	doublesex and mab-3 related transcription factor like family A2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150205	MGI			PMID:22923088
1317799	Fign	fidgetin	gene	MP:0000035	abnormal membranous labyrinth morphology		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017077
1317799	Fign	fidgetin	gene	MP:0000039	abnormal otic capsule morphology		IEA		N	RGD:5509061	20181025	MGI			
1317799	Fign	fidgetin	gene	MP:0000458	abnormal mandible morphology		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0000929	open neural tube		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017077
1317799	Fign	fidgetin	gene	MP:0001306	small lens		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001347	absent lacrimal glands		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001386	abnormal maternal nurturing		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001395	bidirectional circling		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751186
1317799	Fign	fidgetin	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001851	eye inflammation		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001852	conjunctivitis		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001921	reduced fertility		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751186
1317799	Fign	fidgetin	gene	MP:0001967	deafness		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0002116	abnormal craniofacial bone morphology		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017077
1317799	Fign	fidgetin	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017077
1317799	Fign	fidgetin	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:1001817
1317799	Fign	fidgetin	gene	MP:0003161	absent lateral semicircular canal		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0003312	abnormal locomotor coordination		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20150611	MGI			PMID:1181211
1317799	Fign	fidgetin	gene	MP:0004452	abnormal pterygoid process morphology		IEA		N	RGD:5509061	20181025	MGI			
1317799	Fign	fidgetin	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0004748	increased susceptibility to age-related hearing loss		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:1001817
1317799	Fign	fidgetin	gene	MP:0006097	abnormal cerebellar lobule formation		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0008919	fused tarsal bones		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141225	MGI			PMID:1001817
1317799	Fign	fidgetin	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751186
1317799	Fign	fidgetin	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751186
1317799	Fign	fidgetin	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017077
1317799	Fign	fidgetin	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751186
1317799	Fign	fidgetin	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1317799	Fign	fidgetin	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017077
1317799	Fign	fidgetin	gene	MP:0013387	Meibomian gland hypertrophy		IEA		N	RGD:5509061	20141225	MGI			
1317799	Fign	fidgetin	gene	MP:0013447	Harderian gland hypertrophy		IEA		N	RGD:5509061	20150205	MGI			
1317799	Fign	fidgetin	gene	MP:0030233	absent mandibular canal		IEA		N	RGD:5509061	20171019	MGI			
1317799	Fign	fidgetin	gene	MP:0030235	absent mandibular foramen		IEA		N	RGD:5509061	20171019	MGI			
1317799	Fign	fidgetin	gene	MP:0030237	absent mental foramen		IEA		N	RGD:5509061	20171019	MGI			
1317799	Fign	fidgetin	gene	MP:0030796	hip dislocation		IEA		N	RGD:5509061	20181018	MGI			
1317799	Fign	fidgetin	gene	MP:0030838	abnormal acetabular fossa morphology		IEA		N	RGD:5509061	20181025	MGI			
1317799	Fign	fidgetin	gene	MP:0030842	absent subarcuate fossa		IEA		N	RGD:5509061	20181025	MGI			
1317799	Fign	fidgetin	gene	MP:0031432	cornea perforation		IEA		N	RGD:5509061	20220721	MGI			
1317802	Ccnb2	cyclin B2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539739
1317802	Ccnb2	cyclin B2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539739
1317802	Ccnb2	cyclin B2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539739
1317802	Ccnb2	cyclin B2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539739
1317802	Ccnb2	cyclin B2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539739
1317806	Sgsm1	small G protein signaling modulator 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1317806	Sgsm1	small G protein signaling modulator 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1317806	Sgsm1	small G protein signaling modulator 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1317806	Sgsm1	small G protein signaling modulator 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1317810	Ctsf	cathepsin F	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317810	Ctsf	cathepsin F	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508006
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844538
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0001806	decreased IgM level		IEA		N	RGD:5509061	20181011	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844538
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844538
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844538
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0004939	abnormal B cell morphology		IEA		N	RGD:5509061	20190404	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20181011	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20181011	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20150108	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0008037	abnormal T cell morphology		IEA		N	RGD:5509061	20190404	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20190328	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190404	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190328	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844538
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0009853	decreased Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844538
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20150108	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20160804	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20181011	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0010848	decreased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190328	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844538
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20150108	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:20844538
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20181011	MGI			
1317812	Elmo1	engulfment and cell motility 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:20844538
1317818	C2cd4b	C2 calcium-dependent domain containing 4B	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1317818	C2cd4b	C2 calcium-dependent domain containing 4B	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1317818	C2cd4b	C2 calcium-dependent domain containing 4B	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20181227	MGI			
1317818	C2cd4b	C2 calcium-dependent domain containing 4B	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1317818	C2cd4b	C2 calcium-dependent domain containing 4B	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1317818	C2cd4b	C2 calcium-dependent domain containing 4B	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20210128	MGI			
1317818	C2cd4b	C2 calcium-dependent domain containing 4B	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160707	MGI			PMID:27038752
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20240523	MGI			
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0010258	polar cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20230810	MGI			PMID:18385072
1317823	Gje1	gap junction protein, epsilon 1	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:18385072
1317825	Cul3	cullin 3	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339333
1317825	Cul3	cullin 3	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0000839	hypothalamus hyperplasia		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500095
1317825	Cul3	cullin 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500095
1317825	Cul3	cullin 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500095
1317825	Cul3	cullin 3	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339333
1317825	Cul3	cullin 3	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20170615	MGI			PMID:26490675
1317825	Cul3	cullin 3	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339333
1317825	Cul3	cullin 3	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0004043	abnormal pH regulation		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500095
1317825	Cul3	cullin 3	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500095
1317825	Cul3	cullin 3	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500095
1317825	Cul3	cullin 3	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0006300	abnormal entorhinal cortex morphology		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0010092	increased circulating magnesium level		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500095
1317825	Cul3	cullin 3	gene	MP:0010770	preweaning lethality		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339333
1317825	Cul3	cullin 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500095
1317825	Cul3	cullin 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20170615	MGI			PMID:26490675
1317825	Cul3	cullin 3	gene	MP:0012339	hyperkalemia		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20160407	MGI			PMID:26286618
1317825	Cul3	cullin 3	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17339333
1317825	Cul3	cullin 3	gene	MP:0014375	increased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0014382	increased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1317825	Cul3	cullin 3	gene	MP:0020511	decreased dendritic spine length		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317825	Cul3	cullin 3	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20230706	MGI			PMID:33727673
1317827	Guca1b	guanylate cyclase activator 1B	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493703
1317827	Guca1b	guanylate cyclase activator 1B	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18723510
1317827	Guca1b	guanylate cyclase activator 1B	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21123569
1317827	Guca1b	guanylate cyclase activator 1B	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493703
1317827	Guca1b	guanylate cyclase activator 1B	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173221
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0000494	abnormal cecum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575219
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575219
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575219
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20141003	MGI			
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575219
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20160804	MGI			
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575219
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575219
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0005103	abnormal retina pigmentation		IEA		N	RGD:5509061	20141003	MGI			
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20190103	MGI			
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0013481	abnormal ileum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:22575219
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:22575219
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317830	Slc9a8	solute carrier family 9 (sodium/hydrogen exchanger), member 8	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20220324	MGI			PMID:28476888
1317832	Nanos1	nanos C2HC-type zinc finger 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834871
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317833	Slurp2	secreted Ly6/Plaur domain containing 2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20180621	MGI			PMID:26967477
1317836	Dennd2c	DENN domain containing 2C	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1317836	Dennd2c	DENN domain containing 2C	gene	MP:0011625	cystolithiasis		IEA		N	RGD:5509061	20210128	MGI			
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20241121	MGI			
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8706134
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20151112	MGI			PMID:21679928
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20151112	MGI			PMID:21679928
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8706134
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:8706134
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8706134
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20151112	MGI			PMID:21679928
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9712664
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:9712664
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20151112	MGI			PMID:21679928
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002068	abnormal parental behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8706134
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20151112	MGI			PMID:21679928
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20181227	MGI			
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003194	abnormal frequency of paradoxical sleep		IAGP		N	RGD:5509061	20141003	MGI			PMID:11039731
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20151112	MGI			PMID:21679928
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20151112	MGI			PMID:21679928
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:8668344
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20151112	MGI			PMID:21679928
1317838	Fosb	Fos B proto-oncogene, AP-1 transcription factor subunit	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:21679928
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569927
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17868091
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239343
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239343
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239343
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239343
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0000856	abnormal cerebellar plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239343
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569927
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569927
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870281
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569927
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569927
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870281
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569927
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239343
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870281
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870281
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239343
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569927
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239343
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11447289
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870281
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17868091
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870281
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870281
1317843	Frs2	fibroblast growth factor receptor substrate 2	gene	MP:0030250	frontonasal prominence hypoplasia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1317847	Etnk1	ethanolamine kinase 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1317847	Etnk1	ethanolamine kinase 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1317851	Iars1	isoleucyl-tRNA synthetase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:37108118
1317851	Iars1	isoleucyl-tRNA synthetase 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20231109	MGI			PMID:37108118
1317851	Iars1	isoleucyl-tRNA synthetase 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20231109	MGI			PMID:37108118
1317851	Iars1	isoleucyl-tRNA synthetase 1	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20231109	MGI			PMID:37108118
1317852	Dnajb6	DnaJ heat shock protein family (Hsp40) member B6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021343
1317852	Dnajb6	DnaJ heat shock protein family (Hsp40) member B6	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021343
1317852	Dnajb6	DnaJ heat shock protein family (Hsp40) member B6	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021343
1317852	Dnajb6	DnaJ heat shock protein family (Hsp40) member B6	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021343
1317852	Dnajb6	DnaJ heat shock protein family (Hsp40) member B6	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021343
1317852	Dnajb6	DnaJ heat shock protein family (Hsp40) member B6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10021343
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210826	MGI			
1317856	Abhd17c	abhydrolase domain containing 17C	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20210826	MGI			
1317858	Klhdc1	kelch domain containing 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20230601	MGI			
1317862	Chst12	carbohydrate sulfotransferase 12	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317862	Chst12	carbohydrate sulfotransferase 12	gene	MP:0004692	small pubis		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1317867	Ess2	ess-2 splicing factor	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20231130	MGI			PMID:35933014
1317867	Ess2	ess-2 splicing factor	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20231130	MGI			PMID:35933014
1317867	Ess2	ess-2 splicing factor	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20231130	MGI			PMID:35933014
1317867	Ess2	ess-2 splicing factor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20231130	MGI			PMID:35933014
1317867	Ess2	ess-2 splicing factor	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20231130	MGI			PMID:35933014
1317867	Ess2	ess-2 splicing factor	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20231130	MGI			PMID:35933014
1317867	Ess2	ess-2 splicing factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20231130	MGI			PMID:35933014
1317867	Ess2	ess-2 splicing factor	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IAGP		N	RGD:5509061	20231130	MGI			PMID:35933014
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20251211	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0000524	decreased renal tubule number		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0000928	incomplete rostral neuropore closure		IEA		N	RGD:5509061	20251211	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0001948	vesicoureteral reflux		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20150903	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20251211	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20251211	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20251211	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0003623	hydrocele		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0006031	abnormal pharyngeal pouch morphology		IEA		N	RGD:5509061	20251211	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0011803	double kidney pelvis		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0012098	increased spongiotrophoblast size		IEA		N	RGD:5509061	20251211	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230119	MGI			
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0013319	seminal vesicle atrophy		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0020343	abnormal ureteric bud number		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0031286	unilateral cryptorchism		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0031287	bilateral cryptorchism		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317869	Zmym2	zinc finger, MYM-type 2	gene	MP:0031310	abnormal cyst		IAGP		N	RGD:5509061	20250710	MGI			PMID:40313719
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317875	Rad9b	RAD9 checkpoint clamp component B	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20842695
1317877	Rag1	recombination activating 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20170209	MGI			PMID:17218256
1317877	Rag1	recombination activating 1	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:17611620
1317877	Rag1	recombination activating 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1317877	Rag1	recombination activating 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19109567
1317877	Rag1	recombination activating 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:16272283
1317877	Rag1	recombination activating 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751419
1317877	Rag1	recombination activating 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20170209	MGI			PMID:17681821
1317877	Rag1	recombination activating 1	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22773809
1317877	Rag1	recombination activating 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1317877	Rag1	recombination activating 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20170209	MGI			PMID:22770884
1317877	Rag1	recombination activating 1	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17442925
1317877	Rag1	recombination activating 1	gene	MP:0000726	absent lymphocyte		IAGP		N	RGD:5509061	20170209	MGI			PMID:14645513
1317877	Rag1	recombination activating 1	gene	MP:0000726	absent lymphocyte		IAGP		N	RGD:5509061	20170209	MGI			PMID:23995678
1317877	Rag1	recombination activating 1	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:10632602
1317877	Rag1	recombination activating 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20170209	MGI			PMID:10632602
1317877	Rag1	recombination activating 1	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20170209	MGI			PMID:19501000
1317877	Rag1	recombination activating 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20170209	MGI			PMID:16880407
1317877	Rag1	recombination activating 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20170209	MGI			PMID:19501000
1317877	Rag1	recombination activating 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20170209	MGI			PMID:15845450
1317877	Rag1	recombination activating 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20170209	MGI			PMID:16880407
1317877	Rag1	recombination activating 1	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20170209	MGI			PMID:16880407
1317877	Rag1	recombination activating 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20170209	MGI			PMID:24029918
1317877	Rag1	recombination activating 1	gene	MP:0001214	skin hyperplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:24029918
1317877	Rag1	recombination activating 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:16880407
1317877	Rag1	recombination activating 1	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20170209	MGI			PMID:16880407
1317877	Rag1	recombination activating 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1317877	Rag1	recombination activating 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20170209	MGI			PMID:17681821
1317877	Rag1	recombination activating 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18354038
1317877	Rag1	recombination activating 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1317877	Rag1	recombination activating 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17611620
1317877	Rag1	recombination activating 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:24037376
1317877	Rag1	recombination activating 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:19812384
1317877	Rag1	recombination activating 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20240328	MGI			PMID:36037073
1317877	Rag1	recombination activating 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20170209	MGI			PMID:22761313
1317877	Rag1	recombination activating 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20170209	MGI			PMID:10066708
1317877	Rag1	recombination activating 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20170209	MGI			PMID:22761313
1317877	Rag1	recombination activating 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1317877	Rag1	recombination activating 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:14581608
1317877	Rag1	recombination activating 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:18684012
1317877	Rag1	recombination activating 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1317877	Rag1	recombination activating 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:16169499
1317877	Rag1	recombination activating 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:18684012
1317877	Rag1	recombination activating 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20240328	MGI			PMID:36037073
1317877	Rag1	recombination activating 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20170209	MGI			PMID:10411922
1317877	Rag1	recombination activating 1	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20170209	MGI			PMID:18354038
1317877	Rag1	recombination activating 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20170209	MGI			PMID:17218256
1317877	Rag1	recombination activating 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:22888134
1317877	Rag1	recombination activating 1	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:16880407
1317877	Rag1	recombination activating 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751419
1317877	Rag1	recombination activating 1	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20170209	MGI			PMID:14764740
1317877	Rag1	recombination activating 1	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751419
1317877	Rag1	recombination activating 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:17062753
1317877	Rag1	recombination activating 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:17681821
1317877	Rag1	recombination activating 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:15289505
1317877	Rag1	recombination activating 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20170209	MGI			PMID:19590497
1317877	Rag1	recombination activating 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1317877	Rag1	recombination activating 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16272283
1317877	Rag1	recombination activating 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:15782166
1317877	Rag1	recombination activating 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:9584189
1317877	Rag1	recombination activating 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:15782166
1317877	Rag1	recombination activating 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20170209	MGI			PMID:18354038
1317877	Rag1	recombination activating 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:17062753
1317877	Rag1	recombination activating 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:9584189
1317877	Rag1	recombination activating 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18354038
1317877	Rag1	recombination activating 1	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20170209	MGI			PMID:18354038
1317877	Rag1	recombination activating 1	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16272283
1317877	Rag1	recombination activating 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17062753
1317877	Rag1	recombination activating 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:14581608
1317877	Rag1	recombination activating 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:11313471
1317877	Rag1	recombination activating 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:11696599
1317877	Rag1	recombination activating 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:14581608
1317877	Rag1	recombination activating 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:18187659
1317877	Rag1	recombination activating 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:8934569
1317877	Rag1	recombination activating 1	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20170209	MGI			PMID:18354038
1317877	Rag1	recombination activating 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170209	MGI			PMID:15780990
1317877	Rag1	recombination activating 1	gene	MP:0002343	abnormal lymph node cortex morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0002353	abnormal inguinal lymph node morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11696599
1317877	Rag1	recombination activating 1	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20170209	MGI			PMID:22773809
1317877	Rag1	recombination activating 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:14645513
1317877	Rag1	recombination activating 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:15831701
1317877	Rag1	recombination activating 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15021880
1317877	Rag1	recombination activating 1	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:7520000
1317877	Rag1	recombination activating 1	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15021880
1317877	Rag1	recombination activating 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20170209	MGI			PMID:19109567
1317877	Rag1	recombination activating 1	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:19109567
1317877	Rag1	recombination activating 1	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20170209	MGI			PMID:17526724
1317877	Rag1	recombination activating 1	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10762410
1317877	Rag1	recombination activating 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1317877	Rag1	recombination activating 1	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20170209	MGI			PMID:16880407
1317877	Rag1	recombination activating 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20170209	MGI			PMID:11696599
1317877	Rag1	recombination activating 1	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20170209	MGI			PMID:11696599
1317877	Rag1	recombination activating 1	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:15845450
1317877	Rag1	recombination activating 1	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20170209	MGI			PMID:17062753
1317877	Rag1	recombination activating 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17062753
1317877	Rag1	recombination activating 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10632602
1317877	Rag1	recombination activating 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20170209	MGI			PMID:17062753
1317877	Rag1	recombination activating 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20170209	MGI			PMID:17681821
1317877	Rag1	recombination activating 1	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20170209	MGI			PMID:17611620
1317877	Rag1	recombination activating 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20170209	MGI			PMID:10066708
1317877	Rag1	recombination activating 1	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20170209	MGI			PMID:17062753
1317877	Rag1	recombination activating 1	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:10204494
1317877	Rag1	recombination activating 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20170209	MGI			PMID:15845450
1317877	Rag1	recombination activating 1	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20170209	MGI			PMID:10204494
1317877	Rag1	recombination activating 1	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20170209	MGI			PMID:25711213
1317877	Rag1	recombination activating 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751419
1317877	Rag1	recombination activating 1	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:10632602
1317877	Rag1	recombination activating 1	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:18187659
1317877	Rag1	recombination activating 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10632602
1317877	Rag1	recombination activating 1	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17681821
1317877	Rag1	recombination activating 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751419
1317877	Rag1	recombination activating 1	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20170209	MGI			PMID:18187659
1317877	Rag1	recombination activating 1	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17062753
1317877	Rag1	recombination activating 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20170209	MGI			PMID:12498815
1317877	Rag1	recombination activating 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20170209	MGI			PMID:22761313
1317877	Rag1	recombination activating 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:16397132
1317877	Rag1	recombination activating 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:19109567
1317877	Rag1	recombination activating 1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1317877	Rag1	recombination activating 1	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1317877	Rag1	recombination activating 1	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1317877	Rag1	recombination activating 1	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:16880407
1317877	Rag1	recombination activating 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:15782166
1317877	Rag1	recombination activating 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17526724
1317877	Rag1	recombination activating 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14581608
1317877	Rag1	recombination activating 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:22761313
1317877	Rag1	recombination activating 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:15021880
1317877	Rag1	recombination activating 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19285438
1317877	Rag1	recombination activating 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:22761313
1317877	Rag1	recombination activating 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:8934569
1317877	Rag1	recombination activating 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20170209	MGI			PMID:16272283
1317877	Rag1	recombination activating 1	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:17579183
1317877	Rag1	recombination activating 1	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14581608
1317877	Rag1	recombination activating 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17442925
1317877	Rag1	recombination activating 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18684012
1317877	Rag1	recombination activating 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1317877	Rag1	recombination activating 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1317877	Rag1	recombination activating 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20170209	MGI			PMID:10411922
1317877	Rag1	recombination activating 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20190613	MGI			PMID:7520367
1317877	Rag1	recombination activating 1	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20170209	MGI			PMID:10632602
1317877	Rag1	recombination activating 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0005434	absent late pro-B cells		IEA		N	RGD:5509061	20170209	MGI			
1317877	Rag1	recombination activating 1	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20170209	MGI			PMID:15308121
1317877	Rag1	recombination activating 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20170209	MGI			PMID:17611620
1317877	Rag1	recombination activating 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20170209	MGI			PMID:14764740
1317877	Rag1	recombination activating 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20170209	MGI			PMID:15308121
1317877	Rag1	recombination activating 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751419
1317877	Rag1	recombination activating 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:18684012
1317877	Rag1	recombination activating 1	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15021880
1317877	Rag1	recombination activating 1	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317877	Rag1	recombination activating 1	gene	MP:0008041	absent NK T cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:19501000
1317877	Rag1	recombination activating 1	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20240328	MGI			PMID:36037073
1317877	Rag1	recombination activating 1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:19501000
1317877	Rag1	recombination activating 1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20240328	MGI			PMID:36037073
1317877	Rag1	recombination activating 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:10762410
1317877	Rag1	recombination activating 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:16169499
1317877	Rag1	recombination activating 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:16804066
1317877	Rag1	recombination activating 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:15345221
1317877	Rag1	recombination activating 1	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:25343476
1317877	Rag1	recombination activating 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:10762410
1317877	Rag1	recombination activating 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18187659
1317877	Rag1	recombination activating 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20190404	MGI			
1317877	Rag1	recombination activating 1	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1317877	Rag1	recombination activating 1	gene	MP:0008164	abnormal B-1a B cell morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1317877	Rag1	recombination activating 1	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1317877	Rag1	recombination activating 1	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008213	absent immature B cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:14557749
1317877	Rag1	recombination activating 1	gene	MP:0008244	abnormal peritoneal macrophage morphology		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317877	Rag1	recombination activating 1	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:22770884
1317877	Rag1	recombination activating 1	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:22770884
1317877	Rag1	recombination activating 1	gene	MP:0008348	absent gamma-delta T cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:22770884
1317877	Rag1	recombination activating 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:17218256
1317877	Rag1	recombination activating 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20170209	MGI			PMID:19501000
1317877	Rag1	recombination activating 1	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20171228	MGI			PMID:24080084
1317877	Rag1	recombination activating 1	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20170209	MGI			PMID:22550081
1317877	Rag1	recombination activating 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20170209	MGI			PMID:17218256
1317877	Rag1	recombination activating 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:15345221
1317877	Rag1	recombination activating 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:25711213
1317877	Rag1	recombination activating 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:15345221
1317877	Rag1	recombination activating 1	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:10411922
1317877	Rag1	recombination activating 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:15345221
1317877	Rag1	recombination activating 1	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:15345221
1317877	Rag1	recombination activating 1	gene	MP:0008711	increased interleukin-9 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:21600797
1317877	Rag1	recombination activating 1	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20170209	MGI			PMID:9584189
1317877	Rag1	recombination activating 1	gene	MP:0008755	abnormal immunoglobulin V(D)J recombination		IAGP		N	RGD:5509061	20170209	MGI			PMID:10586023
1317877	Rag1	recombination activating 1	gene	MP:0008755	abnormal immunoglobulin V(D)J recombination		IAGP		N	RGD:5509061	20170209	MGI			PMID:1547488
1317877	Rag1	recombination activating 1	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20170209	MGI			PMID:19126872
1317877	Rag1	recombination activating 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20170209	MGI			PMID:10419884
1317877	Rag1	recombination activating 1	gene	MP:0008925	increased cerebellar granule cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17579183
1317877	Rag1	recombination activating 1	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17502664
1317877	Rag1	recombination activating 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20170209	MGI			PMID:17579183
1317877	Rag1	recombination activating 1	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20170209	MGI			PMID:19109567
1317877	Rag1	recombination activating 1	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20170209	MGI			PMID:21179499
1317877	Rag1	recombination activating 1	gene	MP:0010250	absent thymus cortex		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:16751807
1317877	Rag1	recombination activating 1	gene	MP:0010742	increased Schwann cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:10632602
1317877	Rag1	recombination activating 1	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190404	MGI			
1317877	Rag1	recombination activating 1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17611620
1317877	Rag1	recombination activating 1	gene	MP:0010932	increased trabecular bone connectivity density		IAGP		N	RGD:5509061	20170209	MGI			PMID:17611620
1317877	Rag1	recombination activating 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:18563383
1317877	Rag1	recombination activating 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:19501000
1317877	Rag1	recombination activating 1	gene	MP:0011310	abnormal kidney capillary morphology		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0011370	increased mesangial cell apoptosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:17681821
1317877	Rag1	recombination activating 1	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20220505	MGI			PMID:35318366
1317877	Rag1	recombination activating 1	gene	MP:0012563	increased tumor incidence following infection		IAGP		N	RGD:5509061	20241114	MGI			PMID:36103821
1317877	Rag1	recombination activating 1	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20190404	MGI			
1317877	Rag1	recombination activating 1	gene	MP:0013147	limb paralysis		IAGP		N	RGD:5509061	20190613	MGI			PMID:7520367
1317877	Rag1	recombination activating 1	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190404	MGI			
1317877	Rag1	recombination activating 1	gene	MP:0013587	absent thymus medulla		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0014130	thymus cyst		IAGP		N	RGD:5509061	20170209	MGI			PMID:18785974
1317877	Rag1	recombination activating 1	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:18785974
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0014684	impaired spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:25781171
1317880	Lrguk	leucine-rich repeats and guanylate kinase domain containing	gene	MP:0031373	abnormal manchette perinuclear ring morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:25781171
1317886	Eif3l	eukaryotic translation initiation factor 3, subunit L	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1317889	Akr1c12	aldo-keto reductase family 1, member C12	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1317889	Akr1c12	aldo-keto reductase family 1, member C12	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1317891	Carns1	carnosine synthase 1	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20210114	MGI			PMID:33040025
1317891	Carns1	carnosine synthase 1	gene	MP:0020348	decreased olfactory sensory neuron number		IAGP		N	RGD:5509061	20210114	MGI			PMID:33040025
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:29337306
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20240125	MGI			PMID:36056013
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20231102	MGI			PMID:35784893
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20231102	MGI			PMID:35784893
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20231102	MGI			PMID:35784893
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20231102	MGI			PMID:35784893
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20191010	MGI			PMID:29337306
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20231102	MGI			PMID:35784893
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:29337306
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20231102	MGI			PMID:35784893
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:29337306
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20191010	MGI			PMID:29337306
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20231102	MGI			PMID:35784893
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20231102	MGI			PMID:35784893
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20231102	MGI			PMID:35784893
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0009617	decreased brain zinc level		IAGP		N	RGD:5509061	20240125	MGI			PMID:36056013
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20191010	MGI			PMID:29337306
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20191010	MGI			PMID:29337306
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20191010	MGI			PMID:29337306
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20240125	MGI			PMID:36056013
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0020893	abnormal zinc level		IAGP		N	RGD:5509061	20191010	MGI			PMID:29337306
1317895	Slc39a8	solute carrier family 39 (metal ion transporter), member 8	gene	MP:0031173	increased circulating zinc level		IAGP		N	RGD:5509061	20240125	MGI			PMID:36056013
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691482
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0001652	colonic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20160915	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0001806	decreased IgM level		IEA		N	RGD:5509061	20150305	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17882258
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691482
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247480
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IEA		N	RGD:5509061	20160915	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002450	abnormal lymph organ development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002450	abnormal lymph organ development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691482
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691482
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247480
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691482
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691482
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19084435
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20160915	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008167	increased B-1a cell number		IEA		N	RGD:5509061	20160915	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20160915	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20160915	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008400	abnormal CD4-positive, alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247480
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008401	abnormal CD8-positive, alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247480
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581589
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963675
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691482
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0009624	small inguinal lymph nodes		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IAGP		N	RGD:5509061	20180301	MGI			PMID:28846085
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20160915	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20160915	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20160915	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20150305	MGI			
1317897	Rorc	RAR-related orphan receptor gamma	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20150305	MGI			
1317899	Cd209a	CD209a antigen	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1317899	Cd209a	CD209a antigen	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1317899	Cd209a	CD209a antigen	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254286
1317899	Cd209a	CD209a antigen	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1317899	Cd209a	CD209a antigen	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1317899	Cd209a	CD209a antigen	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1317899	Cd209a	CD209a antigen	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1317899	Cd209a	CD209a antigen	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1317899	Cd209a	CD209a antigen	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1317899	Cd209a	CD209a antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1317899	Cd209a	CD209a antigen	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254286
1317905	Tomm7	translocase of outer mitochondrial membrane 7	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20210513	MGI			PMID:30354240
1317905	Tomm7	translocase of outer mitochondrial membrane 7	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20210513	MGI			PMID:30354240
1317905	Tomm7	translocase of outer mitochondrial membrane 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210513	MGI			PMID:30354240
1317905	Tomm7	translocase of outer mitochondrial membrane 7	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20210513	MGI			PMID:30354240
1317905	Tomm7	translocase of outer mitochondrial membrane 7	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20210513	MGI			PMID:30354240
1317905	Tomm7	translocase of outer mitochondrial membrane 7	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20210513	MGI			PMID:30354240
1317910	Coq8a	coenzyme Q8A	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20190926	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0014775	decreased skeletal muscle enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0014781	decreased kidney enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:27499294
1317910	Coq8a	coenzyme Q8A	gene	MP:0014783	decreased liver enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:27499294
1317911	Ms4a4d	membrane-spanning 4-domains, subfamily A, member 4D	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1317911	Ms4a4d	membrane-spanning 4-domains, subfamily A, member 4D	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20241121	MGI			
1317911	Ms4a4d	membrane-spanning 4-domains, subfamily A, member 4D	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932354
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860755
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932354
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789338
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0002619	abnormal lymphocyte morphology		IEA		N	RGD:5509061	20190418	MGI			
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937519
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932354
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860755
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932354
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860755
1317913	Polm	polymerase (DNA directed), mu	gene	MP:0008761	abnormal immunoglobulin light chain V-J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860755
1317915	Pld3	phospholipase D family member 3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210128	MGI			
1317915	Pld3	phospholipase D family member 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20170105	MGI			
1317915	Pld3	phospholipase D family member 3	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0011890	increased circulating ferritin level		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0014495	increased circulating chemokine level		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0014682	increased polyploid hepatocyte number		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0014902	increased circulating CCL2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0031070	hemophagocytosis		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1317915	Pld3	phospholipase D family member 3	gene	MP:0031220	increased circulating CXCL10 level		IAGP		N	RGD:5509061	20210204	MGI			PMID:30111894
1317917	Fer1l4	fer-1 like family member 4	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20200402	MGI			
1317918	Prxl2b	peroxiredoxin like 2B	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20210819	MGI			PMID:33418484
1317918	Prxl2b	peroxiredoxin like 2B	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20210819	MGI			PMID:33418484
1317918	Prxl2b	peroxiredoxin like 2B	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0001985	abnormal gustatory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573884
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573884
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20170608	MGI			PMID:27853148
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20160721	MGI			PMID:24663807
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20170608	MGI			PMID:27853148
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20170608	MGI			PMID:27853148
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20170608	MGI			PMID:27853148
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0008953	abnormal pancreatic somatostatin secretion		IAGP		N	RGD:5509061	20160721	MGI			PMID:24663807
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0010055	abnormal sensory neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20573884
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343897
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20170608	MGI			PMID:27853148
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0011169	abnormal white fat cell differentation		IAGP		N	RGD:5509061	20170608	MGI			PMID:27853148
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0011170	abnormal brown fat cell differentiation		IAGP		N	RGD:5509061	20170608	MGI			PMID:27853148
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20170608	MGI			PMID:27853148
1317920	Ffar4	free fatty acid receptor 4	gene	MP:0020426	abnormal beige fat cell physiology		IAGP		N	RGD:5509061	20170803	MGI			PMID:27853148
1317922	Bin3	bridging integrator 3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317922	Bin3	bridging integrator 3	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339847
1317923	Ctf2	cardiotrophin 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20231109	MGI			PMID:33484199
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:33484199
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20231109	MGI			PMID:33484199
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20231109	MGI			PMID:33484199
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20231109	MGI			PMID:33484199
1317925	Pmepa1	prostate transmembrane protein, androgen induced 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0008285	abnormal hippocampus granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0010011	ectopic hippocampus pyramidal cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0010540	long stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573669
1317927	Apc2	APC regulator of WNT signaling pathway 2	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:22573669
1317931	Mbd3l1	methyl-CpG binding domain protein 3-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15456747
1317931	Mbd3l1	methyl-CpG binding domain protein 3-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18942147
1317932	Ano10	anoctamin 10	gene	MP:0014208	decreased intestinal epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20180503	MGI			PMID:24974903
1317933	Llph	LLP homolog, long-term synaptic facilitation (Aplysia)	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0001629	abnormal heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514127
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786513
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20250605	MGI			PMID:15870258
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0006142	abnormal sinoatrial node conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514127
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0010502	ventricle myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573518
1317935	Myl7	myosin, light polypeptide 7, regulatory	gene	MP:0014731	disorganized myocardial fiber myofibrils		IAGP		N	RGD:5509061	20250904	MGI			PMID:14573518
1317937	Adck1	aarF domain containing kinase 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1317939	Tbx21	T-box 21	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1317939	Tbx21	T-box 21	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1317939	Tbx21	T-box 21	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1317939	Tbx21	T-box 21	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744755
1317939	Tbx21	T-box 21	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1317939	Tbx21	T-box 21	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1317939	Tbx21	T-box 21	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
1317939	Tbx21	T-box 21	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786643
1317939	Tbx21	T-box 21	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1317939	Tbx21	T-box 21	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786643
1317939	Tbx21	T-box 21	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786643
1317939	Tbx21	T-box 21	gene	MP:0002433	abnormal T-helper 1 cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1317939	Tbx21	T-box 21	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1317939	Tbx21	T-box 21	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
1317939	Tbx21	T-box 21	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1317939	Tbx21	T-box 21	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16827899
1317939	Tbx21	T-box 21	gene	MP:0003080	increased natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1317939	Tbx21	T-box 21	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1317939	Tbx21	T-box 21	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16827899
1317939	Tbx21	T-box 21	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1317939	Tbx21	T-box 21	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
1317939	Tbx21	T-box 21	gene	MP:0005340	abnormal susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
1317939	Tbx21	T-box 21	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16827899
1317939	Tbx21	T-box 21	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16827899
1317939	Tbx21	T-box 21	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1317939	Tbx21	T-box 21	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1317939	Tbx21	T-box 21	gene	MP:0008041	absent NK T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1317939	Tbx21	T-box 21	gene	MP:0008041	absent NK T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808259
1317939	Tbx21	T-box 21	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808259
1317939	Tbx21	T-box 21	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1317939	Tbx21	T-box 21	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808259
1317939	Tbx21	T-box 21	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1317939	Tbx21	T-box 21	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1317939	Tbx21	T-box 21	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1317939	Tbx21	T-box 21	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808259
1317939	Tbx21	T-box 21	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20151231	MGI			PMID:24516120
1317939	Tbx21	T-box 21	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1317939	Tbx21	T-box 21	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119024
1317939	Tbx21	T-box 21	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
1317939	Tbx21	T-box 21	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1317939	Tbx21	T-box 21	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1317939	Tbx21	T-box 21	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623380
1317939	Tbx21	T-box 21	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1317939	Tbx21	T-box 21	gene	MP:0008087	decreased T helper 1 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0008090	increased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1317939	Tbx21	T-box 21	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923086
1317939	Tbx21	T-box 21	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623380
1317939	Tbx21	T-box 21	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
1317939	Tbx21	T-box 21	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1317939	Tbx21	T-box 21	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1317939	Tbx21	T-box 21	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24249732
1317939	Tbx21	T-box 21	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665085
1317939	Tbx21	T-box 21	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1317939	Tbx21	T-box 21	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623380
1317939	Tbx21	T-box 21	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623380
1317939	Tbx21	T-box 21	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1317939	Tbx21	T-box 21	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786643
1317939	Tbx21	T-box 21	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200068
1317939	Tbx21	T-box 21	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786643
1317939	Tbx21	T-box 21	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1317939	Tbx21	T-box 21	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786643
1317939	Tbx21	T-box 21	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744755
1317939	Tbx21	T-box 21	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744755
1317939	Tbx21	T-box 21	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744755
1317939	Tbx21	T-box 21	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11786644
1317939	Tbx21	T-box 21	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
1317939	Tbx21	T-box 21	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18635804
1317939	Tbx21	T-box 21	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:21623380
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0000928	incomplete rostral neuropore closure		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0003400	kinked neural tube		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0004180	failure of initiation of embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0011199	abnormal amniotic cavity morphology		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0012099	decreased spongiotrophoblast size		IEA		N	RGD:5509061	20251211	MGI			
1317945	Rprd2	regulation of nuclear pre-mRNA domain containing 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1317947	Plek	pleckstrin	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19190246
1317947	Plek	pleckstrin	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19190246
1317947	Plek	pleckstrin	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19190246
1317949	Kif1b	kinesin family member 1B	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20160811	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0002177	abnormal outer ear morphology		IEA		N	RGD:5509061	20160811	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20160811	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160421	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141106	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11389829
1317949	Kif1b	kinesin family member 1B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20160811	MGI			
1317949	Kif1b	kinesin family member 1B	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1317951	Srpk1	serine/arginine-rich protein specific kinase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24703948
1317951	Srpk1	serine/arginine-rich protein specific kinase 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20191226	MGI			PMID:24703948
1317951	Srpk1	serine/arginine-rich protein specific kinase 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24703948
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210128	MGI			
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20181227	MGI			
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0003450	enlarged pancreas		IEA		N	RGD:5509061	20181227	MGI			
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0009710	anhedonia		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0020379	abnormal sucrose solution preference		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317958	Calhm2	calcium homeostasis modulator family member 2	gene	MP:0021018	decreased dendritic spine number		IAGP		N	RGD:5509061	20250724	MGI			PMID:37493186
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1317962	Wars1	tryptophanyl-tRNA synthetase1	gene	MP:0011897	decreased circulating unsaturated transferrin level		IEA		N	RGD:5509061	20230601	MGI			
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19450229
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051378
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19450229
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706465
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706465
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0003839	abnormal insulin clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051378
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051378
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706465
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051378
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706465
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706465
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0009615	abnormal zinc homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19450229
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0009615	abnormal zinc homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706465
1317969	Slc30a8	solute carrier family 30 (zinc transporter), member 8	gene	MP:0009615	abnormal zinc homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24051378
1317973	Stoml2	stomatin (Epb7.2)-like 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1317973	Stoml2	stomatin (Epb7.2)-like 2	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20231207	MGI			
1317973	Stoml2	stomatin (Epb7.2)-like 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1317973	Stoml2	stomatin (Epb7.2)-like 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1317973	Stoml2	stomatin (Epb7.2)-like 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1317973	Stoml2	stomatin (Epb7.2)-like 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20231207	MGI			
1317973	Stoml2	stomatin (Epb7.2)-like 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200514	MGI			
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871642
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871642
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871642
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0008652	decreased interleukin-1 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871642
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20260402	MGI			
1317978	Lcp1	lymphocyte cytosolic protein 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1317983	Nudt15	nudix hydrolase 15	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20240307	MGI			PMID:31645647
1317983	Nudt15	nudix hydrolase 15	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20240307	MGI			PMID:31645647
1317983	Nudt15	nudix hydrolase 15	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1317983	Nudt15	nudix hydrolase 15	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240307	MGI			PMID:31645647
1317983	Nudt15	nudix hydrolase 15	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20240307	MGI			PMID:31645647
1317983	Nudt15	nudix hydrolase 15	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20240307	MGI			PMID:31645647
1317983	Nudt15	nudix hydrolase 15	gene	MP:0014399	decreased hematopoietic precursor cell number		IAGP		N	RGD:5509061	20240321	MGI			PMID:31645647
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785158
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160421	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210520	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470499
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470499
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785158
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001376	abnormal mating receptivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15465527
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12419415
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15465527
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15465527
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12419415
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210520	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:15465527
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470499
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002716	small male preputial gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470499
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12419415
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470499
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12419415
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0003578	absent ovary		IEA		N	RGD:5509061	20210520	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0003642	absent seminal vesicle		IEA		N	RGD:5509061	20210520	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160421	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0003918	decreased kidney weight		IEA		N	RGD:5509061	20210128	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0003929	decreased heart rate variability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0004156	abnormal QT variability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0004727	absent epididymis		IEA		N	RGD:5509061	20210520	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785158
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785158
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005188	small penis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470499
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005188	small penis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20231207	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12419415
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20220804	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20231207	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0006110	ventricular fibrillation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0006277	abnormal parasympathetic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0006415	absent testes		IEA		N	RGD:5509061	20181227	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785158
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470499
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785158
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15465527
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15465527
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0009014	prolonged proestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15465527
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0009018	short estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15465527
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12419415
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785158
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170202	MGI			PMID:23785158
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0031287	bilateral cryptorchism		IAGP		N	RGD:5509061	20211014	MGI			PMID:9090387
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:15465527
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0031734	doublet premature ventricular contraction		IAGP		N	RGD:5509061	20260716	MGI			PMID:12077327
1317986	Nhlh2	nescient helix loop helix 2	gene	MP:0031735	triplet premature ventricular contraction		IAGP		N	RGD:5509061	20260716	MGI			PMID:12077327
1317988	Nxnl1	nucleoredoxin-like 1	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139892
1317988	Nxnl1	nucleoredoxin-like 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139892
1317988	Nxnl1	nucleoredoxin-like 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139892
1317988	Nxnl1	nucleoredoxin-like 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139892
1317988	Nxnl1	nucleoredoxin-like 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139892
1317988	Nxnl1	nucleoredoxin-like 1	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139892
1317988	Nxnl1	nucleoredoxin-like 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139892
1317988	Nxnl1	nucleoredoxin-like 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139892
1317991	Mmp25	matrix metallopeptidase 25	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1317991	Mmp25	matrix metallopeptidase 25	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20240704	MGI			PMID:27259858
1317991	Mmp25	matrix metallopeptidase 25	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20240704	MGI			PMID:27259858
1317991	Mmp25	matrix metallopeptidase 25	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20240704	MGI			PMID:38570687
1317991	Mmp25	matrix metallopeptidase 25	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20240704	MGI			PMID:38570687
1317991	Mmp25	matrix metallopeptidase 25	gene	MP:0008639	decreased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20240704	MGI			PMID:27259858
1317991	Mmp25	matrix metallopeptidase 25	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20240704	MGI			PMID:27259858
1317991	Mmp25	matrix metallopeptidase 25	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20240704	MGI			PMID:27259858
1317991	Mmp25	matrix metallopeptidase 25	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20240704	MGI			PMID:27259858
1317994	H3f3a	H3.3 histone A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23315948
1317994	H3f3a	H3.3 histone A	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:10556297
1317994	H3f3a	H3.3 histone A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10556297
1317994	H3f3a	H3.3 histone A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10362650
1317994	H3f3a	H3.3 histone A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23315948
1317994	H3f3a	H3.3 histone A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10362650
1317994	H3f3a	H3.3 histone A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23315948
1317994	H3f3a	H3.3 histone A	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10556297
1317996	Rrp8	ribosomal RNA processing 8	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1317996	Rrp8	ribosomal RNA processing 8	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1317996	Rrp8	ribosomal RNA processing 8	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20240523	MGI			
1317996	Rrp8	ribosomal RNA processing 8	gene	MP:0003064	decreased coping response		IEA		N	RGD:5509061	20210128	MGI			
1317996	Rrp8	ribosomal RNA processing 8	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1317996	Rrp8	ribosomal RNA processing 8	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1317996	Rrp8	ribosomal RNA processing 8	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20221215	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20221215	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20231207	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1317998	Atp6v0b	ATPase, H+ transporting, lysosomal V0 subunit B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1318002	Denr	density-regulated protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1318002	Denr	density-regulated protein	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318002	Denr	density-regulated protein	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318002	Denr	density-regulated protein	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318002	Denr	density-regulated protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318002	Denr	density-regulated protein	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1318003	Pdpr	pyruvate dehydrogenase phosphatase regulatory subunit	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1318003	Pdpr	pyruvate dehydrogenase phosphatase regulatory subunit	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20201022	MGI			
1318003	Pdpr	pyruvate dehydrogenase phosphatase regulatory subunit	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20201022	MGI			
1318003	Pdpr	pyruvate dehydrogenase phosphatase regulatory subunit	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20181227	MGI			
1318003	Pdpr	pyruvate dehydrogenase phosphatase regulatory subunit	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1318003	Pdpr	pyruvate dehydrogenase phosphatase regulatory subunit	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1318003	Pdpr	pyruvate dehydrogenase phosphatase regulatory subunit	gene	MP:0012361	decreased large unstained cell number		IEA		N	RGD:5509061	20201022	MGI			
1318003	Pdpr	pyruvate dehydrogenase phosphatase regulatory subunit	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1318008	Eps8l3	EPS8-like 3	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20181227	MGI			
1318008	Eps8l3	EPS8-like 3	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20160421	MGI			
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21600797
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21600797
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20210318	MGI			PMID:32342103
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16717117
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407890
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407890
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005190	osteomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005571	decreased lactate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22753929
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005571	decreased lactate dehydrogenase level		IAGP		N	RGD:5509061	20210318	MGI			PMID:32342103
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008073	abnormal CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008608	increased circulating interleukin-13 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008623	increased circulating interleukin-3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008627	decreased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008629	increased circulating interleukin-9 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002608
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002608
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008656	abnormal interleukin-1 beta secretion		IEA		N	RGD:5509061	20111116	MGI			
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21600797
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407889
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457908
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861349
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21600797
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002608
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22753929
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20181129	MGI			PMID:28847925
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008684	increased interleukin-18 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407890
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002608
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501001
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16717117
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0011072	abnormal macrophage cytokine production		IEA		N	RGD:5509061	20150122	MGI			
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20190131	MGI			PMID:28939830
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0030825	decreased femur size		IAGP		N	RGD:5509061	20181018	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0031110	meningitis		IAGP		N	RGD:5509061	20200910	MGI			PMID:22558291
1318015	Nlrp3	NLR family, pyrin domain containing 3	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:28939830
1318019	Abhd13	abhydrolase domain containing 13	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20200402	MGI			
1318019	Abhd13	abhydrolase domain containing 13	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IEA		N	RGD:5509061	20230720	MGI			
1318019	Abhd13	abhydrolase domain containing 13	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20201022	MGI			
1318019	Abhd13	abhydrolase domain containing 13	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0004597	increased susceptibility to noise-induced hearing loss		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20260129	MGI			PMID:30237157
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1318021	Mrps5	mitochondrial ribosomal protein S5	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1318022	Mtcl2	microtubule crosslinking factor 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20240523	MGI			
1318022	Mtcl2	microtubule crosslinking factor 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20240523	MGI			
1318026	Myf5	myogenic factor 5	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18331721
1318026	Myf5	myogenic factor 5	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18331721
1318026	Myf5	myogenic factor 5	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20160407	MGI			PMID:25725491
1318026	Myf5	myogenic factor 5	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1318026	Myf5	myogenic factor 5	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212806
1318026	Myf5	myogenic factor 5	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0000731	increased collagen deposition in the muscles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14732408
1318026	Myf5	myogenic factor 5	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1318026	Myf5	myogenic factor 5	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1318026	Myf5	myogenic factor 5	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19699733
1318026	Myf5	myogenic factor 5	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1318026	Myf5	myogenic factor 5	gene	MP:0000736	delayed muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17366633
1318026	Myf5	myogenic factor 5	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10929709
1318026	Myf5	myogenic factor 5	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423602
1318026	Myf5	myogenic factor 5	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1318026	Myf5	myogenic factor 5	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
1318026	Myf5	myogenic factor 5	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410975
1318026	Myf5	myogenic factor 5	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1318026	Myf5	myogenic factor 5	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1318026	Myf5	myogenic factor 5	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
1318026	Myf5	myogenic factor 5	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956886
1318026	Myf5	myogenic factor 5	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:24938781
1318026	Myf5	myogenic factor 5	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19954518
1318026	Myf5	myogenic factor 5	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
1318026	Myf5	myogenic factor 5	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
1318026	Myf5	myogenic factor 5	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1318026	Myf5	myogenic factor 5	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
1318026	Myf5	myogenic factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1318026	Myf5	myogenic factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1318026	Myf5	myogenic factor 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956886
1318026	Myf5	myogenic factor 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410975
1318026	Myf5	myogenic factor 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1318026	Myf5	myogenic factor 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1318026	Myf5	myogenic factor 5	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
1318026	Myf5	myogenic factor 5	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
1318026	Myf5	myogenic factor 5	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
1318026	Myf5	myogenic factor 5	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
1318026	Myf5	myogenic factor 5	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423602
1318026	Myf5	myogenic factor 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368734
1318026	Myf5	myogenic factor 5	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121437
1318026	Myf5	myogenic factor 5	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423602
1318026	Myf5	myogenic factor 5	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368734
1318026	Myf5	myogenic factor 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1318026	Myf5	myogenic factor 5	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1318026	Myf5	myogenic factor 5	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20161110	MGI			PMID:26844205
1318026	Myf5	myogenic factor 5	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1318026	Myf5	myogenic factor 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1318026	Myf5	myogenic factor 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410975
1318026	Myf5	myogenic factor 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423602
1318026	Myf5	myogenic factor 5	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368734
1318026	Myf5	myogenic factor 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1318026	Myf5	myogenic factor 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23639729
1318026	Myf5	myogenic factor 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8587605
1318026	Myf5	myogenic factor 5	gene	MP:0002253	abnormal pharyngeal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19531352
1318026	Myf5	myogenic factor 5	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
1318026	Myf5	myogenic factor 5	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20161110	MGI			PMID:26844205
1318026	Myf5	myogenic factor 5	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121437
1318026	Myf5	myogenic factor 5	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20161110	MGI			PMID:26844205
1318026	Myf5	myogenic factor 5	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
1318026	Myf5	myogenic factor 5	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17366633
1318026	Myf5	myogenic factor 5	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1318026	Myf5	myogenic factor 5	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1318026	Myf5	myogenic factor 5	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956886
1318026	Myf5	myogenic factor 5	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0003154	abnormal soft palate morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34557486
1318026	Myf5	myogenic factor 5	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20161110	MGI			PMID:26844205
1318026	Myf5	myogenic factor 5	gene	MP:0003794	delayed somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19531352
1318026	Myf5	myogenic factor 5	gene	MP:0003818	abnormal eye muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19531352
1318026	Myf5	myogenic factor 5	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1318026	Myf5	myogenic factor 5	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
1318026	Myf5	myogenic factor 5	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
1318026	Myf5	myogenic factor 5	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:38829202
1318026	Myf5	myogenic factor 5	gene	MP:0004094	abnormal M line morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368734
1318026	Myf5	myogenic factor 5	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423602
1318026	Myf5	myogenic factor 5	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423602
1318026	Myf5	myogenic factor 5	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
1318026	Myf5	myogenic factor 5	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626014
1318026	Myf5	myogenic factor 5	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
1318026	Myf5	myogenic factor 5	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0004846	absent skeletal muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1318026	Myf5	myogenic factor 5	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0005247	abnormal extraocular muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19531352
1318026	Myf5	myogenic factor 5	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20161110	MGI			PMID:26844205
1318026	Myf5	myogenic factor 5	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
1318026	Myf5	myogenic factor 5	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962509
1318026	Myf5	myogenic factor 5	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1318026	Myf5	myogenic factor 5	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21962509
1318026	Myf5	myogenic factor 5	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666760
1318026	Myf5	myogenic factor 5	gene	MP:0006320	abnormal interscapular fat pad morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0006432	abnormal costal cartilage morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:25725491
1318026	Myf5	myogenic factor 5	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:18331721
1318026	Myf5	myogenic factor 5	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423602
1318026	Myf5	myogenic factor 5	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
1318026	Myf5	myogenic factor 5	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423602
1318026	Myf5	myogenic factor 5	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720708
1318026	Myf5	myogenic factor 5	gene	MP:0008486	decreased muscle spindle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19369542
1318026	Myf5	myogenic factor 5	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212806
1318026	Myf5	myogenic factor 5	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1318026	Myf5	myogenic factor 5	gene	MP:0009137	decreased brown fat lipid droplet number		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1318026	Myf5	myogenic factor 5	gene	MP:0009137	decreased brown fat lipid droplet number		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:24196706
1318026	Myf5	myogenic factor 5	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19699733
1318026	Myf5	myogenic factor 5	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1318026	Myf5	myogenic factor 5	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
1318026	Myf5	myogenic factor 5	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17366633
1318026	Myf5	myogenic factor 5	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1318026	Myf5	myogenic factor 5	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
1318026	Myf5	myogenic factor 5	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
1318026	Myf5	myogenic factor 5	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1318026	Myf5	myogenic factor 5	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
1318026	Myf5	myogenic factor 5	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
1318026	Myf5	myogenic factor 5	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
1318026	Myf5	myogenic factor 5	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1318026	Myf5	myogenic factor 5	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158201
1318026	Myf5	myogenic factor 5	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1318026	Myf5	myogenic factor 5	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1318026	Myf5	myogenic factor 5	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1318026	Myf5	myogenic factor 5	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1318026	Myf5	myogenic factor 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1318026	Myf5	myogenic factor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121437
1318026	Myf5	myogenic factor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1423602
1318026	Myf5	myogenic factor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18331721
1318026	Myf5	myogenic factor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368734
1318026	Myf5	myogenic factor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20241212	MGI			PMID:38829202
1318026	Myf5	myogenic factor 5	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210401	MGI			PMID:29168801
1318026	Myf5	myogenic factor 5	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626014
1318026	Myf5	myogenic factor 5	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20221027	MGI			PMID:34557486
1318026	Myf5	myogenic factor 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1318026	Myf5	myogenic factor 5	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1318026	Myf5	myogenic factor 5	gene	MP:0011170	abnormal brown fat cell differentiation		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368734
1318026	Myf5	myogenic factor 5	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20180726	MGI			PMID:29799007
1318026	Myf5	myogenic factor 5	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1318026	Myf5	myogenic factor 5	gene	MP:0012185	abnormal muscle precursor cell morphology		IAGP		N	RGD:5509061	20211125	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0012186	abnormal muscle precursor cell physiology		IAGP		N	RGD:5509061	20211125	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0012249	absent myotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1318026	Myf5	myogenic factor 5	gene	MP:0012249	absent myotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268580
1318026	Myf5	myogenic factor 5	gene	MP:0013237	abnormal skeletal muscle regeneration		IAGP		N	RGD:5509061	20180726	MGI			PMID:29799007
1318026	Myf5	myogenic factor 5	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1318026	Myf5	myogenic factor 5	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:19699733
1318026	Myf5	myogenic factor 5	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:23562821
1318026	Myf5	myogenic factor 5	gene	MP:0013546	cleft soft palate		IAGP		N	RGD:5509061	20221027	MGI			PMID:34557486
1318026	Myf5	myogenic factor 5	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:21124733
1318026	Myf5	myogenic factor 5	gene	MP:0014396	decreased fat cell mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0014912	decreased fat cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:19954518
1318026	Myf5	myogenic factor 5	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0020520	whitened brown adipose tissue morphology		IAGP		N	RGD:5509061	20180208	MGI			PMID:24703692
1318026	Myf5	myogenic factor 5	gene	MP:0021202	abnormal palatopharyngeus muscle morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34557486
1318026	Myf5	myogenic factor 5	gene	MP:0021204	abnormal superior pharyngeal constrictor muscle morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34557486
1318026	Myf5	myogenic factor 5	gene	MP:0030171	absent extraocular muscles		IAGP		N	RGD:5509061	20171005	MGI			PMID:19531352
1318026	Myf5	myogenic factor 5	gene	MP:0030224	abnormal soft palate muscle morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34557486
1318026	Myf5	myogenic factor 5	gene	MP:0030292	abnormal tensor veli palatini muscle morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34557486
1318026	Myf5	myogenic factor 5	gene	MP:0030294	abnormal levator veli palatini muscle morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:34557486
1318026	Myf5	myogenic factor 5	gene	MP:0030300	upper jaw to lower jaw transformation		IAGP		N	RGD:5509061	20171102	MGI			PMID:25725491
1318026	Myf5	myogenic factor 5	gene	MP:0030957	abnormal myotube morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:11060232
1318026	Myf5	myogenic factor 5	gene	MP:0031328	delayed skeletal muscle regeneration		IAGP		N	RGD:5509061	20220106	MGI			PMID:17366633
1318026	Myf5	myogenic factor 5	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:34557486
1318026	Myf5	myogenic factor 5	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:26844205
1318028	Uba7	ubiquitin-like modifier activating enzyme 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382139
1318028	Uba7	ubiquitin-like modifier activating enzyme 7	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382139
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0001492	abnormal pilomotor reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20231102	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17889673
1318029	Uba6	ubiquitin-like modifier activating enzyme 6	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499007
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220276
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220276
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220276
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220276
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220276
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220276
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220276
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0008409	increased cellular sensitivity to hydroxyurea induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919177
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0011705	absent fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:10921903
1318031	Hus1	HUS1 checkpoint clamp component	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:15919177
1318032	Dennd10	DENN domain containing 10	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1318032	Dennd10	DENN domain containing 10	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1318032	Dennd10	DENN domain containing 10	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1318032	Dennd10	DENN domain containing 10	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1318032	Dennd10	DENN domain containing 10	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230119	MGI			
1318032	Dennd10	DENN domain containing 10	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20260402	MGI			
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:29116649
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20210603	MGI			PMID:29116649
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943600
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943600
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20210603	MGI			PMID:29116649
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20210603	MGI			PMID:29116649
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20210603	MGI			PMID:29116649
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20210603	MGI			PMID:29116649
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:24117625
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0008993	abnormal portal triad morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:29116649
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943600
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943600
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0012293	impaired active avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:24117625
1318037	Wwc1	WW, C2 and coiled-coil domain containing 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:24117625
1318041	Vps29	VPS29 retromer complex component	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20230119	MGI			
1318041	Vps29	VPS29 retromer complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1318042	Eno4	enolase 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0009835	absent sperm annulus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0009837	abnormal sperm end piece morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23446454
1318042	Eno4	enolase 4	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:23446454
1318045	Ubxn10	UBX domain protein 10	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20201022	MGI			
1318045	Ubxn10	UBX domain protein 10	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668895
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22993422
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668895
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21493629
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008644	increased circulating interleukin-12a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008647	increased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008666	increased interleukin-12a secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0009713	enhanced conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339038
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339038
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18690222
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22993422
1318047	Rps6ka5	ribosomal protein S6 kinase A5	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21493629
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383150
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383150
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383150
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383150
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:24204913
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383150
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241078
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0005462	abnormal mast cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24204913
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383150
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383150
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24204913
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383150
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0009869	abnormal descending aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20383150
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318049	Patz1	POZ (BTB) and AT hook containing zinc finger 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22886576
1318051	Stk32a	serine/threonine kinase 32A	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20240822	MGI			PMID:37144879
1318051	Stk32a	serine/threonine kinase 32A	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20240822	MGI			PMID:37144879
1318056	Ly9	lymphocyte antigen 9	gene	MP:0002434	abnormal T-helper 2 cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365421
1318056	Ly9	lymphocyte antigen 9	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365421
1318056	Ly9	lymphocyte antigen 9	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365421
1318057	Slc25a33	solute carrier family 25, member 33	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1318058	Cdh9	cadherin 9	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1318058	Cdh9	cadherin 9	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20180412	MGI			PMID:25126785
1318058	Cdh9	cadherin 9	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1318060	Zfp768	zinc finger protein 768	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318060	Zfp768	zinc finger protein 768	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318060	Zfp768	zinc finger protein 768	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318060	Zfp768	zinc finger protein 768	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318060	Zfp768	zinc finger protein 768	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318060	Zfp768	zinc finger protein 768	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318060	Zfp768	zinc finger protein 768	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318060	Zfp768	zinc finger protein 768	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318060	Zfp768	zinc finger protein 768	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318060	Zfp768	zinc finger protein 768	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11960024
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269252
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22927954
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11960024
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21052544
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11960024
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21052544
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11960024
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14507858
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269252
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19657028
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22927954
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14507858
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19657028
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22927954
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14507858
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22927954
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11960024
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22927954
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22927954
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11960024
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21052544
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:14507858
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22927954
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008581	disorganized photoreceptor inner segment		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21052544
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21052544
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22927954
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20141204	MGI			PMID:25088982
1318062	Rp1	retinitis pigmentosa 1 (human)	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:14507858
1318065	Tcl1	T cell lymphoma breakpoint 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12181493
1318065	Tcl1	T cell lymphoma breakpoint 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12181493
1318067	Trim37	tripartite motif-containing 37	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0003450	enlarged pancreas		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0004806	absent germ cells		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0008526	decreased cranium width		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318067	Trim37	tripartite motif-containing 37	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20160915	MGI			PMID:27044324
1318069	Inf2	inverted formin, FH2 and WH2 domain containing	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1318069	Inf2	inverted formin, FH2 and WH2 domain containing	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20180222	MGI			PMID:29309034
1318069	Inf2	inverted formin, FH2 and WH2 domain containing	gene	MP:0002293	long gestation period		IAGP		N	RGD:5509061	20180222	MGI			PMID:29309034
1318069	Inf2	inverted formin, FH2 and WH2 domain containing	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20180222	MGI			PMID:29309034
1318069	Inf2	inverted formin, FH2 and WH2 domain containing	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20180222	MGI			PMID:29309034
1318069	Inf2	inverted formin, FH2 and WH2 domain containing	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20180222	MGI			PMID:29309034
1318069	Inf2	inverted formin, FH2 and WH2 domain containing	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20180222	MGI			PMID:29309034
1318069	Inf2	inverted formin, FH2 and WH2 domain containing	gene	MP:0011521	decreased placental labyrinth size		IAGP		N	RGD:5509061	20180222	MGI			PMID:29309034
1318071	Cdc7	cell division cycle 7	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1318071	Cdc7	cell division cycle 7	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980714
1318071	Cdc7	cell division cycle 7	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1318071	Cdc7	cell division cycle 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980714
1318071	Cdc7	cell division cycle 7	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1318071	Cdc7	cell division cycle 7	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980714
1318071	Cdc7	cell division cycle 7	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980714
1318071	Cdc7	cell division cycle 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160811	MGI			
1318071	Cdc7	cell division cycle 7	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1318071	Cdc7	cell division cycle 7	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318071	Cdc7	cell division cycle 7	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:14517263
1318071	Cdc7	cell division cycle 7	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:14517263
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332413
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17332413
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210742
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371440
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371440
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371440
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371440
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371440
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20230608	MGI			PMID:17332413
1318073	Ikbke	inhibitor of kappaB kinase epsilon	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17332413
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0003896	prolonged PR interval		IEA		N	RGD:5509061	20211021	MGI			
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0013615	increased volumetric bone mineral density		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0013623	increased femur compact bone thickness		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0013625	increased femur yield load		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0013637	increased femur stiffness		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318075	Rab33b	RAB33B, member RAS oncogene family	gene	MP:0021191	increased bone mineral density of lumbar vertebrae		IAGP		N	RGD:5509061	20230824	MGI			PMID:37359363
1318078	C8a	complement component 8, alpha polypeptide	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1318078	C8a	complement component 8, alpha polypeptide	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1318078	C8a	complement component 8, alpha polypeptide	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1318083	Adamts19	ADAM metallopeptidase with thrombospondin type 1 motif 19	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31844321
1318083	Adamts19	ADAM metallopeptidase with thrombospondin type 1 motif 19	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20210506	MGI			PMID:31844321
1318083	Adamts19	ADAM metallopeptidase with thrombospondin type 1 motif 19	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20210506	MGI			PMID:31844321
1318083	Adamts19	ADAM metallopeptidase with thrombospondin type 1 motif 19	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20210506	MGI			PMID:31844321
1318083	Adamts19	ADAM metallopeptidase with thrombospondin type 1 motif 19	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20210506	MGI			PMID:31844321
1318083	Adamts19	ADAM metallopeptidase with thrombospondin type 1 motif 19	gene	MP:0010595	abnormal aortic valve cusp morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31844321
1318083	Adamts19	ADAM metallopeptidase with thrombospondin type 1 motif 19	gene	MP:0010598	abnormal aortic valve annulus morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31844321
1318083	Adamts19	ADAM metallopeptidase with thrombospondin type 1 motif 19	gene	MP:0011929	abnormal aortic valve flow		IAGP		N	RGD:5509061	20210506	MGI			PMID:31844321
1318083	Adamts19	ADAM metallopeptidase with thrombospondin type 1 motif 19	gene	MP:0031166	abnormal aortic valve commissure morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31844321
1318089	Txnrd3	thioredoxin reductase 3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20221201	MGI			PMID:35753352
1318089	Txnrd3	thioredoxin reductase 3	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20221201	MGI			PMID:35753352
1318089	Txnrd3	thioredoxin reductase 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20221201	MGI			PMID:35753352
1318089	Txnrd3	thioredoxin reductase 3	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20221201	MGI			PMID:35753352
1318090	Pcdhb10	protocadherin beta 10	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1318090	Pcdhb10	protocadherin beta 10	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20260402	MGI			
1318090	Pcdhb10	protocadherin beta 10	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220519	MGI			
1318090	Pcdhb10	protocadherin beta 10	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0000161	scoliosis		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0000825	dilated lateral ventricle		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0001330	abnormal optic nerve morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0001916	intracerebral hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0002279	abnormal diaphragm morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0004057	thin myocardium compact layer		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0004201	fetal growth retardation		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0005244	hemopericardium		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0008536	enlarged third ventricle		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0009770	abnormal optic chiasm morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0009913	abnormal hyoid bone greater horn morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0010589	common truncal valve		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0010592	abnormal atrioventricular septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0011659	interrupted aortic arch, type b		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0013815	abnormal digastric muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0013875	increased trigeminal neuroma incidence		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0013973	abnormal hepatic vein connection		IEA		N	RGD:5509061	20170504	MGI			
1318092	Ssr2	signal sequence receptor, beta	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1318094	Rhpn2	rhophilin, Rho GTPase binding protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1318094	Rhpn2	rhophilin, Rho GTPase binding protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767687
1318094	Rhpn2	rhophilin, Rho GTPase binding protein 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1318094	Rhpn2	rhophilin, Rho GTPase binding protein 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1318094	Rhpn2	rhophilin, Rho GTPase binding protein 2	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1318094	Rhpn2	rhophilin, Rho GTPase binding protein 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1318094	Rhpn2	rhophilin, Rho GTPase binding protein 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1318094	Rhpn2	rhophilin, Rho GTPase binding protein 2	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20191003	MGI			PMID:25071083
1318096	Ermn	ermin, ERM-like protein	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20220210	MGI			PMID:32530539
1318096	Ermn	ermin, ERM-like protein	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:32530539
1318096	Ermn	ermin, ERM-like protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20220210	MGI			PMID:32530539
1318096	Ermn	ermin, ERM-like protein	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1318096	Ermn	ermin, ERM-like protein	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20240523	MGI			
1318096	Ermn	ermin, ERM-like protein	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20190502	MGI			
1318096	Ermn	ermin, ERM-like protein	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20220210	MGI			PMID:32530539
1318098	Mgam	maltase-glucoamylase	gene	MP:0002715	decreased glycogen catabolism rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19193815
1318098	Mgam	maltase-glucoamylase	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19193815
1318098	Mgam	maltase-glucoamylase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17585022
1318098	Mgam	maltase-glucoamylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17585022
1318098	Mgam	maltase-glucoamylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19193815
1318098	Mgam	maltase-glucoamylase	gene	MP:0014982	decreased amylase activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:17585022
1318100	Samhd1	SAM domain and HD domain, 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23972988
1318100	Samhd1	SAM domain and HD domain, 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23972988
1318100	Samhd1	SAM domain and HD domain, 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23972988
1318100	Samhd1	SAM domain and HD domain, 1	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23872947
1318102	Tmem126b	transmembrane protein 126B	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20201224	MGI			PMID:30580996
1318102	Tmem126b	transmembrane protein 126B	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20201224	MGI			PMID:30580996
1318107	Sirt3	sirtuin 3	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20170105	MGI			
1318107	Sirt3	sirtuin 3	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923681
1318107	Sirt3	sirtuin 3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20220630	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1318107	Sirt3	sirtuin 3	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20201231	MGI			
1318107	Sirt3	sirtuin 3	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1318107	Sirt3	sirtuin 3	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20251030	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794531
1318107	Sirt3	sirtuin 3	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0006144	increased systemic arterial systolic blood pressure		IEA		N	RGD:5509061	20111116	MGI			
1318107	Sirt3	sirtuin 3	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856199
1318107	Sirt3	sirtuin 3	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1318107	Sirt3	sirtuin 3	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794531
1318107	Sirt3	sirtuin 3	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21856199
1318109	Plaat5	phospholipase A and acyltransferase 5	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1318109	Plaat5	phospholipase A and acyltransferase 5	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1318109	Plaat5	phospholipase A and acyltransferase 5	gene	MP:0009453	enhanced contextual conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
1318113	Ctrc	chymotrypsin C	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20201231	MGI			
1318113	Ctrc	chymotrypsin C	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20210128	MGI			
1318113	Ctrc	chymotrypsin C	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20200820	MGI			PMID:31211695
1318113	Ctrc	chymotrypsin C	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20200514	MGI			
1318114	Trmt44	tRNA methyltransferase 44	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1318114	Trmt44	tRNA methyltransferase 44	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
1318116	Map3k10	mitogen-activated protein kinase kinase kinase 10	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1318116	Map3k10	mitogen-activated protein kinase kinase kinase 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414056
1318116	Map3k10	mitogen-activated protein kinase kinase kinase 10	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21979919
1318116	Map3k10	mitogen-activated protein kinase kinase kinase 10	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1318116	Map3k10	mitogen-activated protein kinase kinase kinase 10	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21979919
1318116	Map3k10	mitogen-activated protein kinase kinase kinase 10	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21979919
1318118	Cdc42ep5	CDC42 effector protein 5	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20181227	MGI			
1318118	Cdc42ep5	CDC42 effector protein 5	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1318118	Cdc42ep5	CDC42 effector protein 5	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1318118	Cdc42ep5	CDC42 effector protein 5	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10037685
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10037685
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10037685
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10037685
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10037685
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10037685
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588952
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671739
1318127	Mttp	microsomal triglyceride transfer protein	gene	MP:0020515	abnormal visceral yolk sac endoderm morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:9671739
1318129	Zdhhc4	zinc finger, DHHC domain containing 4	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30605677
1318129	Zdhhc4	zinc finger, DHHC domain containing 4	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30605677
1318129	Zdhhc4	zinc finger, DHHC domain containing 4	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20191024	MGI			PMID:30605677
1318129	Zdhhc4	zinc finger, DHHC domain containing 4	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30605677
1318129	Zdhhc4	zinc finger, DHHC domain containing 4	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20191024	MGI			PMID:30605677
1318131	Serinc3	serine incorporator 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210520	MGI			
1318131	Serinc3	serine incorporator 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:32665269
1318131	Serinc3	serine incorporator 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1318131	Serinc3	serine incorporator 3	gene	MP:0010093	decreased circulating magnesium level		IEA		N	RGD:5509061	20150430	MGI			
1318131	Serinc3	serine incorporator 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1318133	Mzf1	myeloid zinc finger 1	gene	MP:0000168	abnormal bone marrow development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445537
1318133	Mzf1	myeloid zinc finger 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445537
1318133	Mzf1	myeloid zinc finger 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445537
1318133	Mzf1	myeloid zinc finger 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445537
1318133	Mzf1	myeloid zinc finger 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445537
1318133	Mzf1	myeloid zinc finger 1	gene	MP:0005649	increased spleen neoplasm incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11445537
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20201022	MGI			
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20201022	MGI			
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20201022	MGI			
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20201022	MGI			
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20201022	MGI			
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200514	MGI			
1318135	Hibch	3-hydroxyisobutyryl-Coenzyme A hydrolase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318144	Odf2l	outer dense fiber of sperm tails 2-like	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1318144	Odf2l	outer dense fiber of sperm tails 2-like	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1318145	Lrrc26	leucine rich repeat containing 26	gene	MP:0005310	abnormal salivary gland physiology		IAGP		N	RGD:5509061	20180111	MGI			PMID:28416688
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0005109	abnormal talus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0010484	bicuspid aortic valve		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0010530	cerebral arteriovenous malformation		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0011493	double ureter		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0012303	umbilical vein stenosis		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0013842	ductus venosus stenosis		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0013843	hepatic portal vein stenosis		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0013844	abnormal perichondrial ossification		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0013845	abnormal eye muscle topology		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0014003	additional anastomosis between intracranial vertebral arteries		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0014019	embryo cyst		IEA		N	RGD:5509061	20170504	MGI			
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0030384	short facial bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0030848	short ilium		IAGP		N	RGD:5509061	20181025	MGI			PMID:16079159
1318148	Chst11	carbohydrate sulfotransferase 11	gene	MP:0030849	wide ilium		IAGP		N	RGD:5509061	20181025	MGI			PMID:16079159
1318159	Hapln4	hyaluronan and proteoglycan link protein 4	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20180830	MGI			PMID:22121037
1318159	Hapln4	hyaluronan and proteoglycan link protein 4	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20180830	MGI			PMID:22121037
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20240229	MGI			PMID:29961073
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207856
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15606908
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15820310
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15820310
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20240229	MGI			PMID:29961073
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15820310
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0003146	absent cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17295842
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0003637	cochlear ganglion hypoplasia		IAGP		N	RGD:5509061	20240229	MGI			PMID:29961073
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15820310
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17295842
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567809
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567809
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567809
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15820310
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17295842
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567809
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20240229	MGI			PMID:29961073
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567809
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004577	abnormal cochlear hair cell inter-stereocilial links morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17295842
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004582	absent cochlear hair bundle ankle links		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004582	absent cochlear hair bundle ankle links		IAGP		N	RGD:5509061	20141003	MGI			PMID:17567809
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004586	pillar cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17295842
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15820310
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15207856
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15606908
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15820310
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775142
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17295842
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1318162	Adgrv1	adhesion G protein-coupled receptor V1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20240229	MGI			PMID:29961073
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20220811	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20220811	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20231207	MGI			
1318166	Krtcap2	keratinocyte associated protein 2	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220811	MGI			
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318169	Sh3rf2	SH3 domain containing ring finger 2	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20200611	MGI			PMID:30540932
1318171	Jph3	junctophilin 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11906164
1318171	Jph3	junctophilin 3	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809425
1318171	Jph3	junctophilin 3	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:16809425
1318173	Hoxd13	homeobox D13	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1318173	Hoxd13	homeobox D13	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1318173	Hoxd13	homeobox D13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1318173	Hoxd13	homeobox D13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1318173	Hoxd13	homeobox D13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1318173	Hoxd13	homeobox D13	gene	MP:0000555	absent carpal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1318173	Hoxd13	homeobox D13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1318173	Hoxd13	homeobox D13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1318173	Hoxd13	homeobox D13	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1318173	Hoxd13	homeobox D13	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1318173	Hoxd13	homeobox D13	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1318173	Hoxd13	homeobox D13	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1318173	Hoxd13	homeobox D13	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1318173	Hoxd13	homeobox D13	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1318173	Hoxd13	homeobox D13	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1318173	Hoxd13	homeobox D13	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1318173	Hoxd13	homeobox D13	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1318173	Hoxd13	homeobox D13	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1318173	Hoxd13	homeobox D13	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1318173	Hoxd13	homeobox D13	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0002772	brachypodia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1318173	Hoxd13	homeobox D13	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0003800	monodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1318173	Hoxd13	homeobox D13	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1318173	Hoxd13	homeobox D13	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1318173	Hoxd13	homeobox D13	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674109
1318173	Hoxd13	homeobox D13	gene	MP:0004576	abnormal embryonic autopod plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1318173	Hoxd13	homeobox D13	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0004636	decreased metacarpal bone number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0004640	decreased metatarsal bone number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0004641	elongated metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0005034	abnormal anus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1318173	Hoxd13	homeobox D13	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8106170
1318173	Hoxd13	homeobox D13	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978698
1318173	Hoxd13	homeobox D13	gene	MP:0006230	iris stroma hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0006401	absent male preputial gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0006401	absent male preputial gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1318173	Hoxd13	homeobox D13	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0009049	abnormal hallux morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0009055	abnormal internal anal sphincter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1318173	Hoxd13	homeobox D13	gene	MP:0009380	abnormal prostate gland ventral lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668621
1318173	Hoxd13	homeobox D13	gene	MP:0009744	postaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19546318
1318173	Hoxd13	homeobox D13	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1318173	Hoxd13	homeobox D13	gene	MP:0013901	absent female preputial gland		IAGP		N	RGD:5509061	20150924	MGI			PMID:9580668
1318173	Hoxd13	homeobox D13	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:8898214
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851961
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964376
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000408	absent duvet hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000424	retarded hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9510031
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511513
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:368650
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6960362
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:723931
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511513
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:4673255
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:6127146
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9510031
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2077109
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:466453
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7352029
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511513
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9510031
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:9510031
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511513
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000888	absent cerebellar granule layer		IEA		N	RGD:5509061	20111116	MGI			
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8346298
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8013566
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8577876
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8848495
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20111116	MGI			
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001524	impaired limb coordination		IEA		N	RGD:5509061	20111116	MGI			
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9510031
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964376
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1565842
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973978
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1590727
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:1590727
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10696797
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9035249
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851961
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8352721
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002277	abnormal respiratory mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973978
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002333	abnormal lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973978
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2230805
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973978
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20160915	MGI			PMID:7667406
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20160915	MGI			PMID:8352721
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1565842
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220519	MGI			
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003126	abnormal external female genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1590727
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2901364
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:1565842
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:1565842
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003684	abnormal inferior olivary complex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511513
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003684	abnormal inferior olivary complex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2231177
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003684	abnormal inferior olivary complex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7842506
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1590727
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2123001
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4673255
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0004494	abnormal synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:6127146
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964376
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851961
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851961
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851961
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11739287
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:32457448
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0008579	abnormal Purkinje cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0008651	increased interleukin-1 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:2230805
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20250731	MGI			PMID:32457448
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511513
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:4673255
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:1590727
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:1590727
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009020	prolonged metestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:1590727
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009942	abnormal olfactory bulb granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009947	abnormal olfactory bulb external plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009949	abnormal olfactory bulb granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009950	abnormal olfactory bulb internal plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1511513
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4673255
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009958	absent cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0009979	abnormal cerebellum deep nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7260600
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0010057	abnormal olfactory bulb outer nerve layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10321020
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520475
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9510031
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:13912552
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0012490	abnormal cochlear VIII nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2077109
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0012575	increased noradrenaline level		IAGP		N	RGD:5509061	20180913	MGI			PMID:6123371
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0013551	decreased cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20161201	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:20722722
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:641237
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0030636	decreased taurine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:6127146
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:6127146
1318176	Rora	RAR-related orphan receptor alpha	gene	MP:0030743	decreased aspartic acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:6127146
1318178	Mcoln3	mucolipin 3	gene	MP:0000048	abnormal stria vascularis morphology		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
1318178	Mcoln3	mucolipin 3	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
1318178	Mcoln3	mucolipin 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0000421	mottled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
1318178	Mcoln3	mucolipin 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0001386	abnormal maternal nurturing		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0001401	jumpy		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0001408	stereotypic behavior		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
1318178	Mcoln3	mucolipin 3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0002622	abnormal cochlear hair cell morphology		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0002826	tonic seizures		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0002856	abnormal vestibular ganglion morphology		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0002857	cochlear ganglion degeneration		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
1318178	Mcoln3	mucolipin 3	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0002939	head spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
1318178	Mcoln3	mucolipin 3	gene	MP:0003150	detached tectorial membrane		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0003312	abnormal locomotor coordination		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0004249	abnormal crista ampullaris morphology		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0004362	cochlear hair cell degeneration		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0004591	enlarged tectorial membrane		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0005175	non-pigmented tail tip		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0005307	head tossing		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0005366	variegated coat color		IEA		N	RGD:5509061	20111116	MGI			
1318178	Mcoln3	mucolipin 3	gene	MP:0009379	abnormal foot pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
1318178	Mcoln3	mucolipin 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:4557539
1318178	Mcoln3	mucolipin 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12209292
1318180	Muc16	mucin 16	gene	MP:0001934	increased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19262696
1318182	Taf8	TATA-box binding protein associated factor 8	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076765
1318182	Taf8	TATA-box binding protein associated factor 8	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076765
1318182	Taf8	TATA-box binding protein associated factor 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210422	MGI			
1318182	Taf8	TATA-box binding protein associated factor 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20221103	MGI			
1318182	Taf8	TATA-box binding protein associated factor 8	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20221103	MGI			
1318190	Garre1	granule associated Rac and RHOG effector 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1318194	1700123O20Rik	RIKEN cDNA 1700123O20 gene	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1318196	Tor1b	torsin family 1, member B	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1318196	Tor1b	torsin family 1, member B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1318196	Tor1b	torsin family 1, member B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1318196	Tor1b	torsin family 1, member B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1318196	Tor1b	torsin family 1, member B	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1318196	Tor1b	torsin family 1, member B	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1318196	Tor1b	torsin family 1, member B	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1318196	Tor1b	torsin family 1, member B	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1318197	Mios	meiosis regulator for oocyte development	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20220324	MGI			PMID:35022234
1318197	Mios	meiosis regulator for oocyte development	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:35022234
1318197	Mios	meiosis regulator for oocyte development	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20220324	MGI			PMID:35022234
1318197	Mios	meiosis regulator for oocyte development	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20220324	MGI			PMID:35022234
1318197	Mios	meiosis regulator for oocyte development	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20220324	MGI			PMID:35022234
1318200	Psmd5	proteasome (prosome, macropain) 26S subunit, non-ATPase, 5	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1318200	Psmd5	proteasome (prosome, macropain) 26S subunit, non-ATPase, 5	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25759215
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20160519	MGI			PMID:25759215
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20160519	MGI			PMID:25759215
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20160519	MGI			PMID:25759215
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20160519	MGI			PMID:25759215
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20160519	MGI			PMID:25759215
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25759215
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25759215
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1318202	Loxl2	lysyl oxidase-like 2	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20160519	MGI			PMID:25759215
1318209	Dgkq	diacylglycerol kinase, theta	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20231207	MGI			
1318209	Dgkq	diacylglycerol kinase, theta	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20210128	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20231207	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20231207	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318212	Lsm8	LSM8 homolog, U6 small nuclear RNA associated	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344997
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11526078
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23494546
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856296
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856296
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856296
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23996959
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856296
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0002711	decreased glucagon secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10217145
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23494546
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856296
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0003647	absent oligodendrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11526078
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0003877	abnormal serotonergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10217145
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10217145
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23494546
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009174	absent pancreatic beta cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23494546
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009186	decreased PP cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009186	decreased PP cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009190	increased pancreatic epsilon cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009190	increased pancreatic epsilon cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23494546
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11526078
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23494546
1318214	Nkx2-2	NK2 homeobox 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584121
1318220	Rab25	RAB25, member RAS oncogene family	gene	MP:0000466	esophageal epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197623
1318220	Rab25	RAB25, member RAS oncogene family	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197623
1318220	Rab25	RAB25, member RAS oncogene family	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197623
1318220	Rab25	RAB25, member RAS oncogene family	gene	MP:0001140	abnormal vagina epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197623
1318220	Rab25	RAB25, member RAS oncogene family	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197623
1318220	Rab25	RAB25, member RAS oncogene family	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197623
1318220	Rab25	RAB25, member RAS oncogene family	gene	MP:0003269	colon polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197623
1318220	Rab25	RAB25, member RAS oncogene family	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197623
1318220	Rab25	RAB25, member RAS oncogene family	gene	MP:0009314	increased colon adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197623
1318223	Septin8	septin 8	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20170629	MGI			PMID:27504968
1318223	Septin8	septin 8	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1318223	Septin8	septin 8	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1318223	Septin8	septin 8	gene	MP:0003313	abnormal locomotor activation		IEA		N	RGD:5509061	20141003	MGI			
1318223	Septin8	septin 8	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20170629	MGI			PMID:27504968
1318223	Septin8	septin 8	gene	MP:0012674	tomacula		IAGP		N	RGD:5509061	20170629	MGI			PMID:27504968
1318225	Sgo2a	shugoshin 2A	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765791
1318225	Sgo2a	shugoshin 2A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765791
1318225	Sgo2a	shugoshin 2A	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765791
1318225	Sgo2a	shugoshin 2A	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765791
1318225	Sgo2a	shugoshin 2A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765791
1318225	Sgo2a	shugoshin 2A	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765791
1318225	Sgo2a	shugoshin 2A	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765791
1318225	Sgo2a	shugoshin 2A	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:18765791
1318230	Rbx1	ring-box 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19325126
1318230	Rbx1	ring-box 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19325126
1318230	Rbx1	ring-box 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19325126
1318230	Rbx1	ring-box 1	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19325126
1318230	Rbx1	ring-box 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19325126
1318230	Rbx1	ring-box 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19325126
1318230	Rbx1	ring-box 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:19325126
1318233	Tmx1	thioredoxin-related transmembrane protein 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170406	MGI			
1318235	Kirrel2	kirre like nephrin family adhesion molecule 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201022	MGI			PMID:27430022
1318235	Kirrel2	kirre like nephrin family adhesion molecule 2	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28815295
1318235	Kirrel2	kirre like nephrin family adhesion molecule 2	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28815295
1318235	Kirrel2	kirre like nephrin family adhesion molecule 2	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28815295
1318235	Kirrel2	kirre like nephrin family adhesion molecule 2	gene	MP:0020360	abnormal asymmetric synapse morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28815295
1318237	Orc3	origin recognition complex, subunit 3	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21185282
1318237	Orc3	origin recognition complex, subunit 3	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20201231	MGI			
1318237	Orc3	origin recognition complex, subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318237	Orc3	origin recognition complex, subunit 3	gene	MP:0020388	decreased radial glial cell number		IAGP		N	RGD:5509061	20161117	MGI			PMID:21185282
1318237	Orc3	origin recognition complex, subunit 3	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20161117	MGI			PMID:21185282
1318241	Rnf149	ring finger protein 149	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20240613	MGI			PMID:37031316
1318241	Rnf149	ring finger protein 149	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20240613	MGI			PMID:37031316
1318241	Rnf149	ring finger protein 149	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20240613	MGI			PMID:37031316
1318241	Rnf149	ring finger protein 149	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20240613	MGI			PMID:37031316
1318241	Rnf149	ring finger protein 149	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20240613	MGI			PMID:37031316
1318241	Rnf149	ring finger protein 149	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20240613	MGI			PMID:37031316
1318242	Meak7	MTOR associated protein, eak-7 homolog	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20181227	MGI			
1318242	Meak7	MTOR associated protein, eak-7 homolog	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1318242	Meak7	MTOR associated protein, eak-7 homolog	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20181227	MGI			
1318247	Tcf15	transcription factor 15	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0000080	abnormal exoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0005421	loose skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0006295	absent sclerotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0008149	abnormal costovertebral joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20171026	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0012248	absent dermatome		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318247	Tcf15	transcription factor 15	gene	MP:0012249	absent myotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955271
1318249	Cbln4	cerebellin 4 precursor protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22220752
1318251	Ctns	cystinosis, nephropathic	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0005544	cornea deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370309
1318251	Ctns	cystinosis, nephropathic	gene	MP:0030622	increased cysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:12370309
1318257	Gskip	GSK3B interacting protein	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0003756	abnormal hard palate morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20160811	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:26582204
1318257	Gskip	GSK3B interacting protein	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:26582204
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471057
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471057
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0003311	aminoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471057
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471057
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471057
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471057
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0011424	decreased urine uric acid level		IAGP		N	RGD:5509061	20230810	MGI			PMID:12471057
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0020400	cystinuria		IAGP		N	RGD:5509061	20161208	MGI			PMID:12471057
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0020405	taurinuria		IAGP		N	RGD:5509061	20161208	MGI			PMID:12471057
1318259	Mocs1	molybdenum cofactor synthesis 1	gene	MP:0031479	increased urine xanthine level		IAGP		N	RGD:5509061	20230810	MGI			PMID:12471057
1318260	Bbs9	Bardet-Biedl syndrome 9	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1318260	Bbs9	Bardet-Biedl syndrome 9	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20181011	MGI			
1318260	Bbs9	Bardet-Biedl syndrome 9	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1318260	Bbs9	Bardet-Biedl syndrome 9	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181011	MGI			
1318260	Bbs9	Bardet-Biedl syndrome 9	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20181011	MGI			
1318260	Bbs9	Bardet-Biedl syndrome 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1318260	Bbs9	Bardet-Biedl syndrome 9	gene	MP:0014142	increased body fat mass		IEA		N	RGD:5509061	20181011	MGI			
1318262	Tpst1	protein-tyrosine sulfotransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964405
1318262	Tpst1	protein-tyrosine sulfotransferase 1	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964405
1318262	Tpst1	protein-tyrosine sulfotransferase 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964405
1318262	Tpst1	protein-tyrosine sulfotransferase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964405
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16283626
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10497154
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16283626
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0010178	increased number of Howell-Jolly bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22910183
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10497154
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16283626
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0011180	abnormal hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24516162
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1318264	Mybl2	Myb proto-oncogene like 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:30600684
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15830394
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20240111	MGI			PMID:37584738
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202188
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:30600684
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002138	abnormal hepatobiliary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202188
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021705
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002697	abnormal eye size		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15830394
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15830394
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20240111	MGI			PMID:37584738
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021705
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20200220	MGI			PMID:30600684
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20240111	MGI			PMID:37584738
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003254	bile duct inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202188
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20200220	MGI			PMID:30600684
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003266	biliary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003266	biliary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202188
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003266	biliary cyst		IAGP		N	RGD:5509061	20200220	MGI			PMID:30600684
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003266	biliary cyst		IAGP		N	RGD:5509061	20240111	MGI			PMID:37584738
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003300	gastrointestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15830394
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202188
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021705
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20200220	MGI			PMID:30600684
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20240111	MGI			PMID:37584738
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15830394
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202188
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021705
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200220	MGI			PMID:30600684
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003334	pancreas fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202188
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202188
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021705
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021705
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003946	renal necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20875407
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0004967	abnormal kidney epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959710
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0005083	abnormal biliary tract morphology		IAGP		N	RGD:5509061	20240111	MGI			PMID:37584738
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0005084	abnormal gallbladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0008737	abnormal spleen physiology		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021705
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20200220	MGI			PMID:30600684
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009143	abnormal pancreatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202188
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009497	abnormal intrahepatic bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009498	abnormal extrahepatic bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009501	abnormal hepatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959710
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0009825	cornea ulcer		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17575307
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011210	abnormal temporomandibular joint morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011331	abnormal papillary duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011352	proximal convoluted tubule brush border loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011359	decreased glomerular capillary number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20875407
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286309
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0012236	abnormal cholangiocyte morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0012238	abnormal cholangiocyte primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519956
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0013611	abnormal bile duct epithelium morphology		IAGP		N	RGD:5509061	20240111	MGI			PMID:37584738
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0014233	bile duct epithelium hyperplasia		IAGP		N	RGD:5509061	20240111	MGI			PMID:37584738
1318267	Pkhd1	polycystic kidney and hepatic disease 1	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20250731	MGI			PMID:37419448
1318269	Drap1	DR1 associated protein 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1318269	Drap1	DR1 associated protein 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1318269	Drap1	DR1 associated protein 1	gene	MP:0002174	abnormal gastrulation movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1318269	Drap1	DR1 associated protein 1	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1318269	Drap1	DR1 associated protein 1	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1318269	Drap1	DR1 associated protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1318269	Drap1	DR1 associated protein 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1318269	Drap1	DR1 associated protein 1	gene	MP:0012184	absent paraxial mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1318269	Drap1	DR1 associated protein 1	gene	MP:0012274	increased axial mesoderm size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471260
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20180201	MGI			PMID:17284606
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23434755
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000316	cellular necrosis		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22281595
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23434755
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000423	delayed hair regrowth		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000424	retarded hair growth		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000469	abnormal esophageal squamous epithelium morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22281595
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000649	sebaceous gland atrophy		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180201	MGI			PMID:17284606
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26842965
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001221	epidermal atrophy		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180201	MGI			PMID:23666760
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20241212	MGI			PMID:36243005
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:23300482
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:23666760
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180201	MGI			PMID:20534480
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180201	MGI			PMID:20534480
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180201	MGI			PMID:20534480
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17284606
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:17284606
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22281595
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20180201	MGI			PMID:20534480
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002006	neoplasm		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:23300482
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29999500
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20180201	MGI			PMID:28207927
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17284606
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20180201	MGI			PMID:17284606
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:17284606
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22281595
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003278	esophageal inflammation		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003380	abnormal intestine regeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:22956684
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003846	matted coat		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20180201	MGI			PMID:23300482
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20211216	MGI			PMID:32555289
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20180329	MGI			PMID:29045572
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20210513	MGI			PMID:32271880
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20180329	MGI			PMID:29045572
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004627	abnormal trochanter morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004675	rib fractures		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23434755
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004987	abnormal osteoblast cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23434755
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20180201	MGI			PMID:22956684
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180201	MGI			PMID:28655914
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20180201	MGI			PMID:24949970
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005397	hematopoietic system phenotype		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20180201	MGI			PMID:28207927
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20241212	MGI			PMID:36243005
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23430111
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008142	decreased small intestinal villus size		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180201	MGI			PMID:23135404
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20180201	MGI			PMID:23430111
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20180201	MGI			PMID:23430111
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008615	decreased circulating interleukin-17 level		IAGP		N	RGD:5509061	20180201	MGI			PMID:22590468
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008800	increased small intestinal crypt cell apoptosis		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20241212	MGI			PMID:36243005
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20180201	MGI			PMID:17284606
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20180201	MGI			PMID:23300482
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21124450
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22281595
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23359070
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009567	mitotic nondisjunction		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009635	enlarged popliteal lymph nodes		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0009794	sebaceous gland hyperplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20180201	MGI			PMID:23300482
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20180201	MGI			PMID:26443207
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20180201	MGI			PMID:23300482
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010537	tumor regression		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208064
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010664	abnormal vitelline artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010862	decreased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:28207927
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20180201	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010897	abnormal bronchiole epithelium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25238791
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20180201	MGI			PMID:22590468
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20180201	MGI			PMID:23274892
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22281595
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011363	renal glomerulus atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371340
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011521	decreased placental labyrinth size		IAGP		N	RGD:5509061	20180201	MGI			PMID:25198863
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0011995	decreased leukemia incidence		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0012204	abnormal neuronal stem cell physiology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0012289	abnormal non-rapid eye movement sleep pattern		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013139	moribund		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013288	premature acrosome reaction		IAGP		N	RGD:5509061	20180329	MGI			PMID:29045572
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20210121	MGI			PMID:32783938
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013585	thymus cortex atrophy		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013586	thymus medulla atrophy		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013626	decreased femur yield load		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013633	decreased femur maximal load		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013638	decreased femur stiffness		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013646	decreased energy dissipated prior to femur fracture		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0013941	abnormal enthesis morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20180201	MGI			PMID:24949970
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35292640
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20180201	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20190221	MGI			PMID:30254136
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:24589777
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:35292640
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:26489471
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20180201	MGI			PMID:28207927
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20180201	MGI			PMID:28655914
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0020427	increased hepatocyte karyomegaly		IAGP		N	RGD:5509061	20221020	MGI			PMID:35672775
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0020444	abnormal intestine apoptosis		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0030484	abnormal osteocyte lacuna morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0030487	abnormal osteocyte dendritic process morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0030827	femur fracture		IAGP		N	RGD:5509061	20181018	MGI			PMID:24419319
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:22505032
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20211118	MGI			PMID:34566982
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1318272	Ndor1	NADPH dependent diflavin oxidoreductase 1	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:26443207
1318275	Sdr42e1	short chain dehydrogenase/reductase family 42E, member 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20181227	MGI			
1318275	Sdr42e1	short chain dehydrogenase/reductase family 42E, member 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
1318277	Sfxn1	sideroflexin 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1318277	Sfxn1	sideroflexin 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20220811	MGI			
1318277	Sfxn1	sideroflexin 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1318277	Sfxn1	sideroflexin 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0005286	decreased saturated fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0008570	lipidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060764
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915479
1318279	Pex7	peroxisomal biogenesis factor 7	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:12915479
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20240523	MGI			
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0004432	abnormal cochlear hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0004523	decreased cochlear hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0004528	fused outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0004533	fused inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0004589	abnormal cochlear hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1318281	Triobp	TRIO and F-actin binding protein	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510926
1318283	Kif12	kinesin family member 12	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0002944	increased lactate dehydrogenase level		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0012602	increased alpha-fetoprotein level		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0014045	Mallory bodies		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318283	Kif12	kinesin family member 12	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20250925	MGI			PMID:39920308
1318286	Dennd4c	DENN domain containing 4C	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318286	Dennd4c	DENN domain containing 4C	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318286	Dennd4c	DENN domain containing 4C	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318286	Dennd4c	DENN domain containing 4C	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318286	Dennd4c	DENN domain containing 4C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318286	Dennd4c	DENN domain containing 4C	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1318290	Nkd1	naked cuticle 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546883
1318290	Nkd1	naked cuticle 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546883
1318290	Nkd1	naked cuticle 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546883
1318290	Nkd1	naked cuticle 1	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1318290	Nkd1	naked cuticle 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1318290	Nkd1	naked cuticle 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1318290	Nkd1	naked cuticle 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546883
1318290	Nkd1	naked cuticle 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1318290	Nkd1	naked cuticle 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546883
1318290	Nkd1	naked cuticle 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546883
1318290	Nkd1	naked cuticle 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1318290	Nkd1	naked cuticle 1	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1318296	Prdm5	PR domain containing 5	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22589746
1318296	Prdm5	PR domain containing 5	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20181227	MGI			
1318296	Prdm5	PR domain containing 5	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1318296	Prdm5	PR domain containing 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1318296	Prdm5	PR domain containing 5	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22589746
1318296	Prdm5	PR domain containing 5	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1318296	Prdm5	PR domain containing 5	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22589746
1318296	Prdm5	PR domain containing 5	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20250508	MGI			
1318296	Prdm5	PR domain containing 5	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20181227	MGI			
1318296	Prdm5	PR domain containing 5	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22589746
1318296	Prdm5	PR domain containing 5	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22589746
1318296	Prdm5	PR domain containing 5	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22589746
1318296	Prdm5	PR domain containing 5	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22589746
1318296	Prdm5	PR domain containing 5	gene	MP:0011642	abnormal bone collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22589746
1318296	Prdm5	PR domain containing 5	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:22589746
1318299	Kif20b	kinesin family member 20B	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1318299	Kif20b	kinesin family member 20B	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20171221	MGI			PMID:28359322
1318299	Kif20b	kinesin family member 20B	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1318299	Kif20b	kinesin family member 20B	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1318299	Kif20b	kinesin family member 20B	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20171221	MGI			PMID:28359322
1318299	Kif20b	kinesin family member 20B	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1318299	Kif20b	kinesin family member 20B	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20171221	MGI			PMID:28359322
1318299	Kif20b	kinesin family member 20B	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1318299	Kif20b	kinesin family member 20B	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28359322
1318299	Kif20b	kinesin family member 20B	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28359322
1318299	Kif20b	kinesin family member 20B	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28359322
1318299	Kif20b	kinesin family member 20B	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28359322
1318299	Kif20b	kinesin family member 20B	gene	MP:0008442	disorganized cortical plate		IAGP		N	RGD:5509061	20171221	MGI			PMID:28359322
1318299	Kif20b	kinesin family member 20B	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0010714	iris coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1318299	Kif20b	kinesin family member 20B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1318299	Kif20b	kinesin family member 20B	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24173802
1318299	Kif20b	kinesin family member 20B	gene	MP:0020337	abnormal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28359322
1318299	Kif20b	kinesin family member 20B	gene	MP:0020850	abnormal microtubule cytoskeleton morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:28359322
1318301	Ogfrl1	opioid growth factor receptor-like 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20260402	MGI			
1318301	Ogfrl1	opioid growth factor receptor-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20250313	MGI			PMID:38699440
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071760
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230601	MGI			
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071760
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071760
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20241121	MGI			
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071760
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071760
1318303	Sp5	trans-acting transcription factor 5	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1318305	Rai1	retinoic acid induced 1	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20663924
1318305	Rai1	retinoic acid induced 1	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0000413	polyphalangy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:20663924
1318305	Rai1	retinoic acid induced 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17024248
1318305	Rai1	retinoic acid induced 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20663924
1318305	Rai1	retinoic acid induced 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20663924
1318305	Rai1	retinoic acid induced 1	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0004472	broad nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517686
1318305	Rai1	retinoic acid induced 1	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20663924
1318305	Rai1	retinoic acid induced 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746153
1318305	Rai1	retinoic acid induced 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:20663924
1318305	Rai1	retinoic acid induced 1	gene	MP:0014124	increased amylin secretion		IAGP		N	RGD:5509061	20160324	MGI			PMID:20663924
1318305	Rai1	retinoic acid induced 1	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1318305	Rai1	retinoic acid induced 1	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170202	MGI			PMID:20663924
1318305	Rai1	retinoic acid induced 1	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:20663924
1318305	Rai1	retinoic acid induced 1	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:15746153
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0003010	decreased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0012415	decreased sarcoma incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20151015	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:25512531
1318309	Rbm38	RNA binding motif protein 38	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:25512531
1318312	Zfp462	zinc finger protein 462	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20181004	MGI			PMID:27621227
1318312	Zfp462	zinc finger protein 462	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20181004	MGI			PMID:27621227
1318312	Zfp462	zinc finger protein 462	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20181004	MGI			PMID:27621227
1318312	Zfp462	zinc finger protein 462	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20181004	MGI			PMID:27621227
1318312	Zfp462	zinc finger protein 462	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20181004	MGI			PMID:27621227
1318312	Zfp462	zinc finger protein 462	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1318312	Zfp462	zinc finger protein 462	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220519	MGI			
1318312	Zfp462	zinc finger protein 462	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20181004	MGI			PMID:27621227
1318312	Zfp462	zinc finger protein 462	gene	MP:0001785	edema		IEA		N	RGD:5509061	20220519	MGI			
1318312	Zfp462	zinc finger protein 462	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20181004	MGI			PMID:27621227
1318312	Zfp462	zinc finger protein 462	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220519	MGI			
1318312	Zfp462	zinc finger protein 462	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1318312	Zfp462	zinc finger protein 462	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220519	MGI			
1318312	Zfp462	zinc finger protein 462	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20181004	MGI			PMID:27621227
1318312	Zfp462	zinc finger protein 462	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1318312	Zfp462	zinc finger protein 462	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20181004	MGI			PMID:27621227
1318312	Zfp462	zinc finger protein 462	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1318314	Srp14	signal recognition particle 14	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1318314	Srp14	signal recognition particle 14	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20250508	MGI			
1318314	Srp14	signal recognition particle 14	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20250508	MGI			
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12637587
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015964
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015964
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015964
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015964
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015964
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015964
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12705864
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015964
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015964
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12705864
1318316	Arhgap5	Rho GTPase activating protein 5	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015964
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20210520	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20170105	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20191212	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20160211	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20181227	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20160114	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160114	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0004973	increased regulatory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20210128	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160114	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0008119	decreased Langerhans cell number		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0008211	decreased mature B cell number		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0008862	asymmetric snout		IAGP		N	RGD:5509061	20191212	MGI			PMID:30707697
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160114	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0013421	increased CD5-positive gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0013430	increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0013513	decreased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1318319	Hbs1l	Hbs1-like (S. cerevisiae)	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0000579	abnormal nail morphology		IEA		N	RGD:5509061	20160421	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20201231	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17942483
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0001064	absent trochlear nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20170105	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160421	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20160421	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434520
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0004082	abnormal habenula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0004106	lymphatic vessel hyperplasia		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20240523	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434520
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890759
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0009945	abnormal accessory olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17942483
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0010197	abnormal lymphatic vessel endothelial cell morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0010368	abnormal lymphatic system physiology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1318328	Sema3f	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318330	Folr2	folate receptor beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508523
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20210128	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230601	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201231	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20201231	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20181227	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230601	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210128	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0005102	abnormal iris pigmentation		IEA		N	RGD:5509061	20230601	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0008966	abnormal chiasmata formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20230601	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:20711356
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20240523	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:17696610
1318332	Trip13	thyroid hormone receptor interactor 13	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:17696610
1318335	Ngly1	N-glycanase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20210923	MGI			PMID:34215698
1318335	Ngly1	N-glycanase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25605922
1318335	Ngly1	N-glycanase 1	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20160407	MGI			
1318335	Ngly1	N-glycanase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210923	MGI			PMID:34215698
1318335	Ngly1	N-glycanase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210923	MGI			PMID:34215698
1318335	Ngly1	N-glycanase 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210923	MGI			PMID:34215698
1318337	Pold4	polymerase (DNA-directed), delta 4	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1318337	Pold4	polymerase (DNA-directed), delta 4	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1318337	Pold4	polymerase (DNA-directed), delta 4	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20230119	MGI			PMID:36356905
1318337	Pold4	polymerase (DNA-directed), delta 4	gene	MP:0010266	decreased liver tumor incidence		IAGP		N	RGD:5509061	20230119	MGI			PMID:36356905
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20230119	MGI			
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230119	MGI			
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230119	MGI			
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318339	Pglyrp4	peptidoglycan recognition protein 4	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709292
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12141427
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12141427
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000328	increased enterocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000478	delayed intestine development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002252	abnormal oropharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12141427
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002363	abnormal spleen marginal sinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0002791	steatorrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0004035	abnormal sublingual gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12141427
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12141427
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008180	abnormal marginal zone B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008240	abnormal spleen marginal zone macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008471	abnormal spleen primary B follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790368
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0009477	small cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10207146
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0013483	abnormal jejunum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:10926756
1318341	Nkx2-3	NK2 homeobox 3	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:12141427
1318345	Ect2	epithelial cell transforming 2	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160421	MGI			
1318345	Ect2	epithelial cell transforming 2	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701760
1318345	Ect2	epithelial cell transforming 2	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701760
1318345	Ect2	epithelial cell transforming 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1318345	Ect2	epithelial cell transforming 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160811	MGI			
1318345	Ect2	epithelial cell transforming 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1318345	Ect2	epithelial cell transforming 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701760
1318345	Ect2	epithelial cell transforming 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318348	Cd5l	CD5 antigen-like	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1318348	Cd5l	CD5 antigen-like	gene	MP:0000579	abnormal nail morphology		IEA		N	RGD:5509061	20160421	MGI			
1318348	Cd5l	CD5 antigen-like	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892623
1318348	Cd5l	CD5 antigen-like	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1318348	Cd5l	CD5 antigen-like	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892623
1318348	Cd5l	CD5 antigen-like	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12598318
1318348	Cd5l	CD5 antigen-like	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210805	MGI			
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17666404
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0002832	coarse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664227
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0005155	herniated intestine		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664227
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17666404
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664227
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0005421	loose skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664227
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0006077	inguinal hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0006238	abnormal choriocapillaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664227
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0008418	abnormal cutaneous elastic fiber morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17872905
1318352	Efemp1	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1318354	Ttc4	tetratricopeptide repeat domain 4	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20230601	MGI			
1318354	Ttc4	tetratricopeptide repeat domain 4	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1318354	Ttc4	tetratricopeptide repeat domain 4	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20241010	MGI			
1318354	Ttc4	tetratricopeptide repeat domain 4	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1318354	Ttc4	tetratricopeptide repeat domain 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1318354	Ttc4	tetratricopeptide repeat domain 4	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20241010	MGI			
1318356	Scand1	SCAN domain-containing 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1318356	Scand1	SCAN domain-containing 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20230601	MGI			
1318356	Scand1	SCAN domain-containing 1	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20230601	MGI			
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000025	otic hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20180705	MGI			PMID:23469164
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20180705	MGI			PMID:23469164
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20180705	MGI			PMID:23469164
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20240704	MGI			PMID:38696583
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20180705	MGI			PMID:23469164
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0002234	abnormal pharynx morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20240704	MGI			PMID:38696583
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0003421	abnormal thyroid gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0003923	abnormal heart left atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0004062	dilated heart right atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0004461	basisphenoid bone hypoplasia		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20180705	MGI			PMID:23469164
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20180705	MGI			PMID:23469164
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20180705	MGI			PMID:23469164
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0009880	decreased mouth size		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0009929	meningomyelocele		IAGP		N	RGD:5509061	20240704	MGI			PMID:38696583
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074029
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12082638
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0013573	abnormal parathyroid gland development		IAGP		N	RGD:5509061	20150305	MGI			PMID:11242111
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0030160	abnormal auditory bulla morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318358	Crkl	Crk like proto-oncogene, adaptor protein	gene	MP:0031463	increased palatal shelf size		IAGP		N	RGD:5509061	20230309	MGI			PMID:25565927
1318360	Meis3	Meis homeobox 3	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20220519	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220519	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20220519	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210826	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210826	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210826	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20220519	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20250508	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220519	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0011045	decreased lung elastance		IEA		N	RGD:5509061	20221215	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0011048	decreased lung tissue damping		IEA		N	RGD:5509061	20221215	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0011625	cystolithiasis		IEA		N	RGD:5509061	20220519	MGI			
1318360	Meis3	Meis homeobox 3	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20220519	MGI			
1318363	Rtbdn	retbindin	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1318363	Rtbdn	retbindin	gene	MP:0002073	abnormal hair growth		IEA		N	RGD:5509061	20201231	MGI			
1318363	Rtbdn	retbindin	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20191024	MGI			PMID:29079576
1318363	Rtbdn	retbindin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20191024	MGI			PMID:29079576
1318363	Rtbdn	retbindin	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20191024	MGI			PMID:29079576
1318363	Rtbdn	retbindin	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1318363	Rtbdn	retbindin	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20150108	MGI			
1318363	Rtbdn	retbindin	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20191024	MGI			PMID:29079576
1318363	Rtbdn	retbindin	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20191024	MGI			PMID:29079576
1318363	Rtbdn	retbindin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20191024	MGI			PMID:29079576
1318363	Rtbdn	retbindin	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20191024	MGI			PMID:29079576
1318363	Rtbdn	retbindin	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20191024	MGI			PMID:29079576
1318363	Rtbdn	retbindin	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20191024	MGI			PMID:29079576
1318366	Coch	cochlin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14657014
1318366	Coch	cochlin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481359
1318366	Coch	cochlin	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697796
1318366	Coch	cochlin	gene	MP:0004814	reduced linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697796
1318366	Coch	cochlin	gene	MP:0004814	reduced linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:21073934
1318366	Coch	cochlin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697796
1318366	Coch	cochlin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21073934
1318371	Kif5c	kinesin family member 5C	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964943
1318371	Kif5c	kinesin family member 5C	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964943
1318371	Kif5c	kinesin family member 5C	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1318371	Kif5c	kinesin family member 5C	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1318371	Kif5c	kinesin family member 5C	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1318371	Kif5c	kinesin family member 5C	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20230601	MGI			
1318371	Kif5c	kinesin family member 5C	gene	MP:0006006	increased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10964943
1318371	Kif5c	kinesin family member 5C	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:21335237
1318372	Utp3	UTP3 small subunit processome component	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20220915	MGI			PMID:35328065
1318372	Utp3	UTP3 small subunit processome component	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20220915	MGI			PMID:35328065
1318372	Utp3	UTP3 small subunit processome component	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220915	MGI			PMID:35328065
1318375	Sirt1	sirtuin 1	gene	MP:0000149	abnormal scapula morphology		IEA		N	RGD:5509061	20201231	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201022	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20201022	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17877786
1318375	Sirt1	sirtuin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17877786
1318375	Sirt1	sirtuin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668205
1318375	Sirt1	sirtuin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20201022	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687325
1318375	Sirt1	sirtuin 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21103071
1318375	Sirt1	sirtuin 1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21103071
1318375	Sirt1	sirtuin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17877786
1318375	Sirt1	sirtuin 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17877786
1318375	Sirt1	sirtuin 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201022	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1318375	Sirt1	sirtuin 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687325
1318375	Sirt1	sirtuin 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21103071
1318375	Sirt1	sirtuin 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687325
1318375	Sirt1	sirtuin 1	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687325
1318375	Sirt1	sirtuin 1	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0003450	enlarged pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20211021	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20201231	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687325
1318375	Sirt1	sirtuin 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20141003	MGI			PMID:17877786
1318375	Sirt1	sirtuin 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20201022	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687325
1318375	Sirt1	sirtuin 1	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0005646	abnormal pituitary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1318375	Sirt1	sirtuin 1	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0008512	disorganized retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0008938	decreased pituitary gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20008932
1318375	Sirt1	sirtuin 1	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20220714	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0009164	exocrine pancreas atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21103071
1318375	Sirt1	sirtuin 1	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0010946	hyperpnea		IAGP		N	RGD:5509061	20170713	MGI			PMID:28273169
1318375	Sirt1	sirtuin 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18335035
1318375	Sirt1	sirtuin 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960381
1318375	Sirt1	sirtuin 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318375	Sirt1	sirtuin 1	gene	MP:0011543	increased urine antidiuretic hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687325
1318375	Sirt1	sirtuin 1	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:22006156
1318375	Sirt1	sirtuin 1	gene	MP:0012298	hypoactivity in response to feed restriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668205
1318375	Sirt1	sirtuin 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0013168	absent hindlimb buds		IAGP		N	RGD:5509061	20150528	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0013604	abnormal adult Leydig cell differentiation		IAGP		N	RGD:5509061	20150319	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20150611	MGI			PMID:17201918
1318375	Sirt1	sirtuin 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:18835033
1318375	Sirt1	sirtuin 1	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:18687325
1318375	Sirt1	sirtuin 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:18987333
1318375	Sirt1	sirtuin 1	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:12482959
1318375	Sirt1	sirtuin 1	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:22006156
1318377	Pura	purine rich element binding protein A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0001391	abnormal tail movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0010897	abnormal bronchiole epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0011149	abnormal hippocampus stratum lacunosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22010047
1318377	Pura	purine rich element binding protein A	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20220310	MGI			PMID:12972605
1318377	Pura	purine rich element binding protein A	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:12972605
1318378	Cfap90	cilia and flagella associated protein 90	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240613	MGI			PMID:38697008
1318380	Zfp422	zinc finger protein 422	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1318380	Zfp422	zinc finger protein 422	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1318380	Zfp422	zinc finger protein 422	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1318380	Zfp422	zinc finger protein 422	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1318380	Zfp422	zinc finger protein 422	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1318380	Zfp422	zinc finger protein 422	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1318380	Zfp422	zinc finger protein 422	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1318380	Zfp422	zinc finger protein 422	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1318380	Zfp422	zinc finger protein 422	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1318380	Zfp422	zinc finger protein 422	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1318380	Zfp422	zinc finger protein 422	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1318383	Crygn	crystallin, gamma N	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20170713	MGI			PMID:27517863
1318383	Crygn	crystallin, gamma N	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1318383	Crygn	crystallin, gamma N	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20170713	MGI			PMID:27517863
1318383	Crygn	crystallin, gamma N	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20170713	MGI			PMID:27517863
1318385	Dhx9	DExH-box helicase 9	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22988576
1318385	Dhx9	DExH-box helicase 9	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20260402	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20260402	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0003895	increased ectoderm apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20240523	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22988576
1318385	Dhx9	DExH-box helicase 9	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0011187	abnormal parietal endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20240523	MGI			
1318385	Dhx9	DExH-box helicase 9	gene	MP:0012105	delayed gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9811865
1318385	Dhx9	DExH-box helicase 9	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:9811865
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:25382142
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:25382142
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28695146
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24647135
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24647135
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:25382142
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20180111	MGI			PMID:25382142
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20150827	MGI			PMID:24647135
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20180111	MGI			PMID:25382142
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20190425	MGI			PMID:28695146
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20170119	MGI			PMID:27748972
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20180111	MGI			PMID:25382142
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20150827	MGI			PMID:24647135
1318393	Mlc1	megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human)	gene	MP:0011854	cerebral edema		IAGP		N	RGD:5509061	20180111	MGI			PMID:25382142
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20181227	MGI			
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20181227	MGI			
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20180412	MGI			PMID:25126785
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0009235	small sperm head		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0014631	abnormal elongated spermatid morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:27677211
1318395	Kcng4	potassium voltage-gated channel, subfamily G, member 4	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210318	MGI			PMID:27677211
1318397	Lca5	Leber congenital amaurosis 5 (human)	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606596
1318397	Lca5	Leber congenital amaurosis 5 (human)	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606596
1318397	Lca5	Leber congenital amaurosis 5 (human)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606596
1318397	Lca5	Leber congenital amaurosis 5 (human)	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606596
1318397	Lca5	Leber congenital amaurosis 5 (human)	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606596
1318397	Lca5	Leber congenital amaurosis 5 (human)	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606596
1318397	Lca5	Leber congenital amaurosis 5 (human)	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606596
1318397	Lca5	Leber congenital amaurosis 5 (human)	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606596
1318397	Lca5	Leber congenital amaurosis 5 (human)	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606596
1318398	Sppl2b	signal peptide peptidase like 2B	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20151217	MGI			PMID:24492962
1318398	Sppl2b	signal peptide peptidase like 2B	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1318398	Sppl2b	signal peptide peptidase like 2B	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1318398	Sppl2b	signal peptide peptidase like 2B	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20151217	MGI			PMID:24492962
1318398	Sppl2b	signal peptide peptidase like 2B	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20151217	MGI			PMID:24492962
1318398	Sppl2b	signal peptide peptidase like 2B	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0003653	decreased skin turgor		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318401	Rap1gds1	RAP1, GTP-GDP dissociation stimulator 1	gene	MP:0013182	increased spinal cord apoptosis		IAGP		N	RGD:5509061	20201231	MGI			PMID:10793158
1318404	Nkiras1	NFKB inhibitor interacting Ras-like protein 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20240523	MGI			
1318404	Nkiras1	NFKB inhibitor interacting Ras-like protein 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11254677
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11254677
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11254677
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392163
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19305396
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11254677
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19662682
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19662682
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713979
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392163
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11254677
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713979
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18258848
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19305396
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18504307
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12928364
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17615242
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392163
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514610
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19305396
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19305396
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392163
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19305396
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12928364
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11254677
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19305396
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19662682
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514610
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0006173	abnormal myeloid dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11254677
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0006173	abnormal myeloid dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19305396
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19305396
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392163
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008197	abnormal follicular dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713979
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008198	abnormal follicular dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713979
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008244	abnormal peritoneal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008399	abnormal alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12928364
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008400	abnormal CD4-positive, alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12928364
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008401	abnormal CD8-positive, alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12928364
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18258848
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18258848
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19662682
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18258848
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18258848
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514610
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514610
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0008895	abnormal intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843382
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210826	MGI			
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0011077	decreased macrophage nitric oxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694574
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0014472	impaired B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:17392163
1318407	Ccr6	C-C motif chemokine receptor 6	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:10843382
1318419	L3mbtl2	L3MBTL2 polycomb repressive complex 1 subunit	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20161216	MGI			PMID:22770845
1318419	L3mbtl2	L3MBTL2 polycomb repressive complex 1 subunit	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20150430	MGI			
1318419	L3mbtl2	L3MBTL2 polycomb repressive complex 1 subunit	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20161216	MGI			PMID:22770845
1318419	L3mbtl2	L3MBTL2 polycomb repressive complex 1 subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20161216	MGI			PMID:22770845
1318419	L3mbtl2	L3MBTL2 polycomb repressive complex 1 subunit	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318419	L3mbtl2	L3MBTL2 polycomb repressive complex 1 subunit	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20161216	MGI			PMID:22770845
1318419	L3mbtl2	L3MBTL2 polycomb repressive complex 1 subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318419	L3mbtl2	L3MBTL2 polycomb repressive complex 1 subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318419	L3mbtl2	L3MBTL2 polycomb repressive complex 1 subunit	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318421	Atad1	ATPase family, AAA domain containing 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21496646
1318421	Atad1	ATPase family, AAA domain containing 1	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21496646
1318421	Atad1	ATPase family, AAA domain containing 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21496646
1318421	Atad1	ATPase family, AAA domain containing 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21496646
1318421	Atad1	ATPase family, AAA domain containing 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21496646
1318421	Atad1	ATPase family, AAA domain containing 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:21496646
1318421	Atad1	ATPase family, AAA domain containing 1	gene	MP:0008431	abnormal short-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:21496646
1318421	Atad1	ATPase family, AAA domain containing 1	gene	MP:0011002	enhanced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21496646
1318421	Atad1	ATPase family, AAA domain containing 1	gene	MP:0014373	increased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240328	MGI			PMID:21496646
1318423	Myoz3	myozenin 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1318428	Cldn8	claudin 8	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0003016	increased circulating bicarbonate level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0003028	alkalosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0004119	hypokalemia		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0005628	decreased circulating potassium level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318428	Cldn8	claudin 8	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25831548
1318433	Osgep	O-sialoglycoprotein endopeptidase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1318433	Osgep	O-sialoglycoprotein endopeptidase	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1318435	H3c2	H3 clustered histone 2	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1318435	H3c2	H3 clustered histone 2	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1318435	H3c2	H3 clustered histone 2	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1318435	H3c2	H3 clustered histone 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200521	MGI			PMID:32142668
1318436	Dipk1a	divergent protein kinase domain 1A	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1318436	Dipk1a	divergent protein kinase domain 1A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20170105	MGI			
1318436	Dipk1a	divergent protein kinase domain 1A	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1318436	Dipk1a	divergent protein kinase domain 1A	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1318436	Dipk1a	divergent protein kinase domain 1A	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180503	MGI			PMID:29323231
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200402	MGI			
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180503	MGI			PMID:29323231
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20200402	MGI			
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20220811	MGI			
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20180503	MGI			PMID:29323231
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180503	MGI			PMID:29323231
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20180503	MGI			PMID:29323231
1318438	Shmt2	serine hydroxymethyltransferase 2 (mitochondrial)	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1318441	Tsen15	tRNA splicing endonuclease subunit 15	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20250508	MGI			
1318441	Tsen15	tRNA splicing endonuclease subunit 15	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1318441	Tsen15	tRNA splicing endonuclease subunit 15	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1318444	Oasl1	2'-5' oligoadenylate synthetase-like 1	gene	MP:0008548	abnormal circulating interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23416614
1318444	Oasl1	2'-5' oligoadenylate synthetase-like 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1318444	Oasl1	2'-5' oligoadenylate synthetase-like 1	gene	MP:0020938	decreased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200514	MGI			PMID:23416614
1318444	Oasl1	2'-5' oligoadenylate synthetase-like 1	gene	MP:0031039	decreased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:23416614
1318446	Slc37a1	solute carrier family 37 (glycerol-3-phosphate transporter), member 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1318446	Slc37a1	solute carrier family 37 (glycerol-3-phosphate transporter), member 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20181227	MGI			
1318446	Slc37a1	solute carrier family 37 (glycerol-3-phosphate transporter), member 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1318446	Slc37a1	solute carrier family 37 (glycerol-3-phosphate transporter), member 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1318446	Slc37a1	solute carrier family 37 (glycerol-3-phosphate transporter), member 1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20210128	MGI			
1318448	Loxl4	lysyl oxidase-like 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1318448	Loxl4	lysyl oxidase-like 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1318450	Il18r1	interleukin 18 receptor 1	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227969
1318450	Il18r1	interleukin 18 receptor 1	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227969
1318450	Il18r1	interleukin 18 receptor 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10227969
1318450	Il18r1	interleukin 18 receptor 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:24176642
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24176642
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24176642
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0004569	glossopharyngeal nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934123
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24176642
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24176642
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24176642
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0009879	abnormal arcus anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951254
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:24176642
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:24176642
1318454	Tasp1	taspase, threonine aspartase 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:24176642
1318461	Kif23	kinesin family member 23	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230914	MGI			PMID:32818800
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20170105	MGI			PMID:26123588
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0002050	increased pheochromocytoma incidence		IAGP		N	RGD:5509061	20170105	MGI			PMID:26123588
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220519	MGI			
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170105	MGI			PMID:26123588
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20180111	MGI			PMID:28204537
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:5509061	20180111	MGI			PMID:28204537
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20241121	MGI			
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0010147	abnormal endocrine pancreas physiology		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20170105	MGI			PMID:26123588
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318464	Sdhb	succinate dehydrogenase complex, subunit B, iron sulfur (Ip)	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20220804	MGI			PMID:35472723
1318468	Ark2n	arkadia (RNF111) N-terminal like PKA signaling regulator 2N	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:35882232
1318468	Ark2n	arkadia (RNF111) N-terminal like PKA signaling regulator 2N	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20221201	MGI			PMID:35882232
1318468	Ark2n	arkadia (RNF111) N-terminal like PKA signaling regulator 2N	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20221201	MGI			PMID:35882232
1318468	Ark2n	arkadia (RNF111) N-terminal like PKA signaling regulator 2N	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20221201	MGI			PMID:35882232
1318468	Ark2n	arkadia (RNF111) N-terminal like PKA signaling regulator 2N	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20221201	MGI			PMID:35882232
1318468	Ark2n	arkadia (RNF111) N-terminal like PKA signaling regulator 2N	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20221201	MGI			PMID:35882232
1318468	Ark2n	arkadia (RNF111) N-terminal like PKA signaling regulator 2N	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20221201	MGI			PMID:35882232
1318468	Ark2n	arkadia (RNF111) N-terminal like PKA signaling regulator 2N	gene	MP:0014145	increased white adipose tissue mass		IAGP		N	RGD:5509061	20221201	MGI			PMID:35882232
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20260402	MGI			
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20260402	MGI			
1318470	Lrp11	low density lipoprotein receptor-related protein 11	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20260402	MGI			
1318472	Wars2	tryptophanyl tRNA synthetase 2 (mitochondrial)	gene	MP:0000955	abnormal spinal cord morphology		IEA		N	RGD:5509061	20210826	MGI			
1318472	Wars2	tryptophanyl tRNA synthetase 2 (mitochondrial)	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1318472	Wars2	tryptophanyl tRNA synthetase 2 (mitochondrial)	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1318472	Wars2	tryptophanyl tRNA synthetase 2 (mitochondrial)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318472	Wars2	tryptophanyl tRNA synthetase 2 (mitochondrial)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1318472	Wars2	tryptophanyl tRNA synthetase 2 (mitochondrial)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318472	Wars2	tryptophanyl tRNA synthetase 2 (mitochondrial)	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20801882
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549527
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20801882
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20801882
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0002241	abnormal laryngeal mucosa goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759516
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20801882
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549527
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549527
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0010790	abnormal stomach pyloric antrum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20801882
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20801882
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0010863	absent respiratory mucosa goblet cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759516
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20801882
1318474	Spdef	SAM pointed domain containing ets transcription factor	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:19549527
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106902
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:31943697
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106902
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106902
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:31943697
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20211104	MGI			PMID:31943697
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106902
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106902
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0005283	increased unsaturated fatty acids level		IAGP		N	RGD:5509061	20211104	MGI			PMID:31943697
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0005285	decreased unsaturated fatty acids level		IAGP		N	RGD:5509061	20211104	MGI			PMID:31943697
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106902
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0006149	decreased visual acuity		IAGP		N	RGD:5509061	20211104	MGI			PMID:31943697
1318476	Elovl2	ELOVL fatty acid elongase 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106902
1318478	Klk14	kallikrein related-peptidase 14	gene	MP:0002959	increased urine microalbumin level		IEA		N	RGD:5509061	20211021	MGI			
1318478	Klk14	kallikrein related-peptidase 14	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1318478	Klk14	kallikrein related-peptidase 14	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1318481	Alkbh4	alkB homolog 4, lysine demethylase	gene	MP:0003707	increased cell nucleus count		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673617
1318481	Alkbh4	alkB homolog 4, lysine demethylase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673617
1318481	Alkbh4	alkB homolog 4, lysine demethylase	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673617
1318481	Alkbh4	alkB homolog 4, lysine demethylase	gene	MP:0013289	abnormal mitotic cytokinesis		IAGP		N	RGD:5509061	20190718	MGI			PMID:23673617
1318481	Alkbh4	alkB homolog 4, lysine demethylase	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:23673617
1318483	Pop1	processing of precursor 1, ribonuclease P/MRP family, (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393806
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567973
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567973
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738878
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393806
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393806
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567973
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738878
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393806
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393806
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738878
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393806
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567973
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393806
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16642288
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16642288
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:16642288
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16642288
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738878
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567973
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738878
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393806
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567973
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393806
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567973
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738878
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567973
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16642288
1318485	Slc19a2	solute carrier family 19 (thiamine transporter), member 2	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:14738878
1318487	Mrgbp	MRG/MORF4L binding protein	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20220811	MGI			
1318487	Mrgbp	MRG/MORF4L binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1318487	Mrgbp	MRG/MORF4L binding protein	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0005400	abnormal vitamin level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0005665	increased circulating noradrenaline level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0020237	increased proline level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0030647	increased ornithine level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0030659	decreased glycine level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0030691	increased serine level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0030697	increased phenylalanine level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0030722	decreased lysine level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318490	Aldh7a1	aldehyde dehydrogenase family 7, member A1	gene	MP:0030747	increased leucine level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32969477
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20240523	MGI			
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20240523	MGI			
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20240523	MGI			
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0009908	protruding tongue		IEA		N	RGD:5509061	20240523	MGI			
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1318492	Slc35a3	solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20230504	MGI			PMID:37053259
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:19624305
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0001499	abnormal kindling response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19624305
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230601	MGI			
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0002193	minimal clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19624305
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0002194	maximal tonic hindlimb extension seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19624305
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19624305
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19624305
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19624305
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19624305
1318493	Szt2	SZT2 subunit of KICSTOR complex	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19624305
1318495	Zfp287	zinc finger protein 287	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20170105	MGI			
1318497	Tagap1	T cell activation GTPase activating protein 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1318497	Tagap1	T cell activation GTPase activating protein 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1318497	Tagap1	T cell activation GTPase activating protein 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20220519	MGI			
1318497	Tagap1	T cell activation GTPase activating protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1318497	Tagap1	T cell activation GTPase activating protein 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1318497	Tagap1	T cell activation GTPase activating protein 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20220519	MGI			
1318497	Tagap1	T cell activation GTPase activating protein 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1318497	Tagap1	T cell activation GTPase activating protein 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1318500	Zfp334	zinc finger protein 334	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1318500	Zfp334	zinc finger protein 334	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1318500	Zfp334	zinc finger protein 334	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20181227	MGI			
1318500	Zfp334	zinc finger protein 334	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20210128	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20230601	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0002892	decreased superior colliculus size		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0004081	abnormal globus pallidus morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20220811	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0008282	enlarged hippocampus		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0008914	enlarged cerebellum		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0009849	increased vertical stereotypic behavior		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0010058	enlarged olfactory bulb		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20210128	MGI			
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0012489	abnormal retrosplenial region morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318504	Pdzd8	PDZ domain containing 8	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20220825	MGI			PMID:35227461
1318507	Neu4	sialidase 4	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18270209
1318507	Neu4	sialidase 4	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18270209
1318507	Neu4	sialidase 4	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18270209
1318507	Neu4	sialidase 4	gene	MP:0005283	increased unsaturated fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18270209
1318507	Neu4	sialidase 4	gene	MP:0031632	increased lung cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18270209
1318508	Gtf2a1l	general transcription factor IIA, 1-like	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1318508	Gtf2a1l	general transcription factor IIA, 1-like	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20240523	MGI			
1318514	Crybg1	crystallin beta-gamma domain containing 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1318514	Crybg1	crystallin beta-gamma domain containing 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1318514	Crybg1	crystallin beta-gamma domain containing 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1318514	Crybg1	crystallin beta-gamma domain containing 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20160421	MGI			
1318514	Crybg1	crystallin beta-gamma domain containing 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1318514	Crybg1	crystallin beta-gamma domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1318514	Crybg1	crystallin beta-gamma domain containing 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22069191
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22069191
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22069191
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535917
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535917
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535917
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510869
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22069191
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22069191
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535917
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22069191
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510869
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535917
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535917
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510869
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510869
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22069191
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22069191
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510869
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535917
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22069191
1318518	Maml1	mastermind like transcriptional coactivator 1	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1318523	Amn	amnionless	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20150219	MGI			
1318523	Amn	amnionless	gene	MP:0000484	abnormal pulmonary artery morphology		IEA		N	RGD:5509061	20150219	MGI			
1318523	Amn	amnionless	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660894
1318523	Amn	amnionless	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20150219	MGI			
1318523	Amn	amnionless	gene	MP:0001625	cardiac hypertrophy		IEA		N	RGD:5509061	20150219	MGI			
1318523	Amn	amnionless	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660894
1318523	Amn	amnionless	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851841
1318523	Amn	amnionless	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660894
1318523	Amn	amnionless	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851841
1318523	Amn	amnionless	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11279523
1318523	Amn	amnionless	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660894
1318523	Amn	amnionless	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9825865
1318523	Amn	amnionless	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851841
1318523	Amn	amnionless	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9825865
1318523	Amn	amnionless	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660894
1318523	Amn	amnionless	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851841
1318523	Amn	amnionless	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20150219	MGI			
1318523	Amn	amnionless	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660894
1318523	Amn	amnionless	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851841
1318523	Amn	amnionless	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660894
1318523	Amn	amnionless	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851841
1318523	Amn	amnionless	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660894
1318523	Amn	amnionless	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851841
1318523	Amn	amnionless	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20150219	MGI			
1318523	Amn	amnionless	gene	MP:0010488	abnormal left subclavian artery morphology		IEA		N	RGD:5509061	20150219	MGI			
1318523	Amn	amnionless	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660894
1318523	Amn	amnionless	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11279523
1318523	Amn	amnionless	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9851841
1318523	Amn	amnionless	gene	MP:0011666	double outlet right ventricle, ventricular defect committed to aorta		IEA		N	RGD:5509061	20150219	MGI			
1318523	Amn	amnionless	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:9825865
1318526	Ccdc90b	coiled-coil domain containing 90B	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20241121	MGI			
1318529	Dkk4	dickkopf WNT signaling pathway inhibitor 4	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20170105	MGI			
1318529	Dkk4	dickkopf WNT signaling pathway inhibitor 4	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1318529	Dkk4	dickkopf WNT signaling pathway inhibitor 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1318529	Dkk4	dickkopf WNT signaling pathway inhibitor 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1318532	Txnl4a	thioredoxin-like 4A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1318537	Slfn2	schlafen 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20160915	MGI			
1318537	Slfn2	schlafen 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20160915	MGI			
1318537	Slfn2	schlafen 2	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20160915	MGI			
1318537	Slfn2	schlafen 2	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:20190759
1318537	Slfn2	schlafen 2	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:20190759
1318540	Abtb3	ankyrin repeat and BTB domain containing 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1318540	Abtb3	ankyrin repeat and BTB domain containing 3	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1318540	Abtb3	ankyrin repeat and BTB domain containing 3	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1318540	Abtb3	ankyrin repeat and BTB domain containing 3	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1318540	Abtb3	ankyrin repeat and BTB domain containing 3	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1318540	Abtb3	ankyrin repeat and BTB domain containing 3	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:37261953
1318540	Abtb3	ankyrin repeat and BTB domain containing 3	gene	MP:0020422	decreased freezing behavior		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1318540	Abtb3	ankyrin repeat and BTB domain containing 3	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1318540	Abtb3	ankyrin repeat and BTB domain containing 3	gene	MP:0021010	impaired synaptic physiology		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1318542	Sntb2	syntrophin, basic 2	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548643
1318542	Sntb2	syntrophin, basic 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548643
1318542	Sntb2	syntrophin, basic 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548643
1318542	Sntb2	syntrophin, basic 2	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548643
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743826
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743826
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318545	Sema5a	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15743826
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606593
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23266956
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:21283818
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451056
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23790753
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23266956
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160331	MGI			PMID:25252692
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060709
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060709
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889149
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956081
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15480979
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956081
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311138
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160915	MGI			PMID:21283818
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24295069
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24295069
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24295069
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060709
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003269	colon polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003269	colon polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311138
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003299	gastric polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956081
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003299	gastric polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060709
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003299	gastric polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003299	gastric polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003299	gastric polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:15480979
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003299	gastric polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003299	gastric polyps		IAGP		N	RGD:5509061	20160915	MGI			PMID:21283818
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956081
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003334	pancreas fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23266956
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266325
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606593
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060709
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172296
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18245476
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004870	small premaxilla		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004902	abnormal uterus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005044	sepsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18840652
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266325
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266325
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23597566
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266325
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606593
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24295069
1318549	Stk11	serine/threonine kinase 11	gene	MP:0006038	increased mitochondrial fission		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23790753
1318549	Stk11	serine/threonine kinase 11	gene	MP:0006342	absent first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:15480979
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:18245476
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008012	duodenum polyps		IAGP		N	RGD:5509061	20150702	MGI			PMID:12218179
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008256	abnormal myometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23241891
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008717	increased lung squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008718	increased lung large cell carcinoma incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:17676035
1318549	Stk11	serine/threonine kinase 11	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009145	abnormal pancreatic acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009181	decreased pancreatic delta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:21283818
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009552	urinary bladder obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142330
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009552	urinary bladder obstruction		IAGP		N	RGD:5509061	20160915	MGI			PMID:21283818
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009656	delayed chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1318549	Stk11	serine/threonine kinase 11	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311138
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23790753
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451056
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956081
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278673
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451056
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010322	increased cutaneous melanoma incidence		IAGP		N	RGD:5509061	20160331	MGI			PMID:25252692
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010352	gastrointestinal tract polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010352	gastrointestinal tract polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:18311138
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060709
1318549	Stk11	serine/threonine kinase 11	gene	MP:0010906	abnormal lung bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23266956
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23266956
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15889149
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956081
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12226664
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060709
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23266956
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060709
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22791749
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011766	abnormal urinary bladder mucosa morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:21283818
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011874	enlarged urinary bladder		IAGP		N	RGD:5509061	20160915	MGI			PMID:21283818
1318549	Stk11	serine/threonine kinase 11	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266325
1318549	Stk11	serine/threonine kinase 11	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0013220	increased pancreas apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:18227155
1318549	Stk11	serine/threonine kinase 11	gene	MP:0013267	first pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0013328	visceromegaly		IAGP		N	RGD:5509061	20141204	MGI			PMID:16357136
1318549	Stk11	serine/threonine kinase 11	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23790753
1318549	Stk11	serine/threonine kinase 11	gene	MP:0014660	increased skin nevi incidence		IAGP		N	RGD:5509061	20250508	MGI			PMID:25252692
1318549	Stk11	serine/threonine kinase 11	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20260521	MGI			PMID:37541209
1318549	Stk11	serine/threonine kinase 11	gene	MP:0030022	decreased muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:15889149
1318549	Stk11	serine/threonine kinase 11	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0030266	small vomer bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:27527806
1318549	Stk11	serine/threonine kinase 11	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:11509733
1318549	Stk11	serine/threonine kinase 11	gene	MP:0031407	increased Sertoli cell proliferation		IAGP		N	RGD:5509061	20220630	MGI			PMID:22791749
1318554	Lamc1	laminin, gamma 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0000756	forelimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873583
1318554	Lamc1	laminin, gamma 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17942732
1318554	Lamc1	laminin, gamma 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003557	absent vas deferens		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003558	absent uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873583
1318554	Lamc1	laminin, gamma 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0003826	abnormal Mullerian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003827	abnormal Wolffian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1318554	Lamc1	laminin, gamma 1	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0004220	abnormal peripheral nervous system regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873583
1318554	Lamc1	laminin, gamma 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638863
1318554	Lamc1	laminin, gamma 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0005623	abnormal meninges morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873583
1318554	Lamc1	laminin, gamma 1	gene	MP:0008030	abnormal Cajal-Retzius cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873583
1318554	Lamc1	laminin, gamma 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122064
1318554	Lamc1	laminin, gamma 1	gene	MP:0010225	abnormal quadriceps morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0010451	kidney microaneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0010742	increased Schwann cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22767514
1318554	Lamc1	laminin, gamma 1	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20191114	MGI			PMID:30456378
1318554	Lamc1	laminin, gamma 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1318554	Lamc1	laminin, gamma 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9885251
1318554	Lamc1	laminin, gamma 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1318554	Lamc1	laminin, gamma 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9885251
1318554	Lamc1	laminin, gamma 1	gene	MP:0011206	absent visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:9885251
1318554	Lamc1	laminin, gamma 1	gene	MP:0011366	absent metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015298
1318554	Lamc1	laminin, gamma 1	gene	MP:0020452	abnormal axon radial sorting		IAGP		N	RGD:5509061	20170914	MGI			PMID:14638863
1318556	Thoc1	THO complex 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20240523	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20240523	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20240523	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17211872
1318556	Thoc1	THO complex 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17211872
1318556	Thoc1	THO complex 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17211872
1318556	Thoc1	THO complex 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17211872
1318556	Thoc1	THO complex 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20240523	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705185
1318556	Thoc1	THO complex 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20240523	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230119	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705185
1318556	Thoc1	THO complex 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230119	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705185
1318556	Thoc1	THO complex 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17211872
1318556	Thoc1	THO complex 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17211872
1318556	Thoc1	THO complex 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20240523	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20240523	MGI			
1318556	Thoc1	THO complex 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16705185
1318558	Pla2g4b	phospholipase A2, group IVB (cytosolic)	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1318558	Pla2g4b	phospholipase A2, group IVB (cytosolic)	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1318558	Pla2g4b	phospholipase A2, group IVB (cytosolic)	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1318564	Arhgap45	Rho GTPase activating protein 45	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:33719206
1318564	Arhgap45	Rho GTPase activating protein 45	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:33719206
1318564	Arhgap45	Rho GTPase activating protein 45	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:33719206
1318564	Arhgap45	Rho GTPase activating protein 45	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:33719206
1318564	Arhgap45	Rho GTPase activating protein 45	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20211209	MGI			PMID:33719206
1318564	Arhgap45	Rho GTPase activating protein 45	gene	MP:0008185	decreased naive B cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:33719206
1318564	Arhgap45	Rho GTPase activating protein 45	gene	MP:0010130	decreased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:33719206
1318564	Arhgap45	Rho GTPase activating protein 45	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:33719206
1318564	Arhgap45	Rho GTPase activating protein 45	gene	MP:0031207	decreased lymphocyte chemotaxis		IAGP		N	RGD:5509061	20211209	MGI			PMID:33719206
1318568	Cdk2ap1	cyclin dependent kinase 2 associated protein 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:19229340
1318568	Cdk2ap1	cyclin dependent kinase 2 associated protein 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19229340
1318568	Cdk2ap1	cyclin dependent kinase 2 associated protein 1	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19229340
1318568	Cdk2ap1	cyclin dependent kinase 2 associated protein 1	gene	MP:0030046	round forehead		IAGP		N	RGD:5509061	20170921	MGI			PMID:19229340
1318571	Proz	protein Z, vitamin K-dependent plasma glycoprotein	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10829076
1318571	Proz	protein Z, vitamin K-dependent plasma glycoprotein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10829076
1318571	Proz	protein Z, vitamin K-dependent plasma glycoprotein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10829076
1318571	Proz	protein Z, vitamin K-dependent plasma glycoprotein	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10829076
1318571	Proz	protein Z, vitamin K-dependent plasma glycoprotein	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344422
1318571	Proz	protein Z, vitamin K-dependent plasma glycoprotein	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200924	MGI			PMID:18344422
1318573	Fbln1	fibulin 1	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1318573	Fbln1	fibulin 1	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1318573	Fbln1	fibulin 1	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0003499	thyroid gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0004568	fusion of glossopharyngeal and vagus nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0006203	eye hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0008816	petechiae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0008816	petechiae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0010405	ostium secundum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0010502	ventricle myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0011359	decreased glomerular capillary number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564885
1318573	Fbln1	fibulin 1	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538758
1318573	Fbln1	fibulin 1	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:18538758
1318575	Lingo1	leucine rich repeat and Ig domain containing 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15895088
1318577	Foxp1	forkhead box P1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1318577	Foxp1	forkhead box P1	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16819554
1318577	Foxp1	forkhead box P1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965654
1318577	Foxp1	forkhead box P1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1318577	Foxp1	forkhead box P1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1318577	Foxp1	forkhead box P1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16819554
1318577	Foxp1	forkhead box P1	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16819554
1318577	Foxp1	forkhead box P1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347093
1318577	Foxp1	forkhead box P1	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0003115	abnormal respiratory system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1318577	Foxp1	forkhead box P1	gene	MP:0003159	abnormal esophageal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0003160	abnormal esophagus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0003808	increased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0003808	increased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1318577	Foxp1	forkhead box P1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0004548	dilated esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1318577	Foxp1	forkhead box P1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965654
1318577	Foxp1	forkhead box P1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965654
1318577	Foxp1	forkhead box P1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965654
1318577	Foxp1	forkhead box P1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16819554
1318577	Foxp1	forkhead box P1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347093
1318577	Foxp1	forkhead box P1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0010588	conotruncal ridge hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0010856	dilated respiratory conducting tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0010949	decreased club cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1318577	Foxp1	forkhead box P1	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1318577	Foxp1	forkhead box P1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16819554
1318577	Foxp1	forkhead box P1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318577	Foxp1	forkhead box P1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347093
1318577	Foxp1	forkhead box P1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342473
1318577	Foxp1	forkhead box P1	gene	MP:0011148	decreased mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428829
1318577	Foxp1	forkhead box P1	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:20713518
1318577	Foxp1	forkhead box P1	gene	MP:0014726	abnormal cardiomyocyte maturation		IAGP		N	RGD:5509061	20250911	MGI			PMID:20713518
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000576	clubfoot		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000962	disorganized dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0002809	increased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17573772
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18003640
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18459960
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105374
1318579	Fkbp8	FK506 binding protein 8	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:18003640
1318581	Mtrr	5-methyltetrahydrofolate-homocysteine methyltransferase reductase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17369066
1318581	Mtrr	5-methyltetrahydrofolate-homocysteine methyltransferase reductase	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17369066
1318581	Mtrr	5-methyltetrahydrofolate-homocysteine methyltransferase reductase	gene	MP:0006076	abnormal circulating homocysteine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17369066
1318581	Mtrr	5-methyltetrahydrofolate-homocysteine methyltransferase reductase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1318581	Mtrr	5-methyltetrahydrofolate-homocysteine methyltransferase reductase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:17369066
1318581	Mtrr	5-methyltetrahydrofolate-homocysteine methyltransferase reductase	gene	MP:0030645	decreased circulating methionine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:17369066
1318584	Papola	poly (A) polymerase alpha	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1318584	Papola	poly (A) polymerase alpha	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210826	MGI			
1318584	Papola	poly (A) polymerase alpha	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1318584	Papola	poly (A) polymerase alpha	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1318584	Papola	poly (A) polymerase alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20190502	MGI			
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170518	MGI			PMID:25416620
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20170518	MGI			PMID:25416620
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0001983	abnormal olfactory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20160811	MGI			
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25416620
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0005499	abnormal olfactory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1318586	Gng13	guanine nucleotide binding protein (G protein), gamma 13	gene	MP:0011677	abnormal olfactory sensory neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637188
1318593	Tiam2	T cell lymphoma invasion and metastasis 2	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20191003	MGI			PMID:30817801
1318595	Rpl11	ribosomal protein L11	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210401	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20210325	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:26489471
1318595	Rpl11	ribosomal protein L11	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:26489471
1318598	Mnt	max binding protein	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16740691
1318598	Mnt	max binding protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970171
1318598	Mnt	max binding protein	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970171
1318598	Mnt	max binding protein	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970171
1318598	Mnt	max binding protein	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16740691
1318598	Mnt	max binding protein	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0004441	small occipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0004476	absent palatine bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970171
1318598	Mnt	max binding protein	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16740691
1318598	Mnt	max binding protein	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12970171
1318598	Mnt	max binding protein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318598	Mnt	max binding protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15028671
1318599	Ccdc102a	coiled-coil domain containing 102A	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20250508	MGI			
1318601	Ddx23	DEAD box helicase 23	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1318601	Ddx23	DEAD box helicase 23	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620299
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0002102	abnormal ear morphology		IEA		N	RGD:5509061	20240523	MGI			
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20181882
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620299
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620299
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620299
1318603	Ikzf2	IKAROS family zinc finger 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620299
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20201022	MGI			
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555575
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20241121	MGI			
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555575
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555575
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554722
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555575
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20241121	MGI			
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555575
1318605	Ptp4a3	protein tyrosine phosphatase 4a3	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0000480	increased rib number		IEA		N	RGD:5509061	20160114	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0000600	liver hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0000819	abnormal olfactory bulb morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0002191	abnormal artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0002237	abnormal nasal cavity morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0002249	abnormal larynx morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0003078	aphakia		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0003387	aorta coarctation		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0004057	thin myocardium compact layer		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0004163	abnormal adenohypophysis morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0004181	abnormal carotid artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0005236	abnormal olfactory nerve morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0005587	abnormal Meckel's cartilage morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0010912	herniated liver		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0011513	abnormal vertebral artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20180726	MGI			PMID:29799007
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0012303	umbilical vein stenosis		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013237	abnormal skeletal muscle regeneration		IAGP		N	RGD:5509061	20180726	MGI			PMID:29799007
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013809	absent pectinate muscle		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013833	absent olfactory nerve		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013875	increased trigeminal neuroma incidence		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013945	abnormal elbow joint morphology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013975	abnormal coronary sinus connection		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013985	abnormal umbilical vein topology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0014003	additional anastomosis between intracranial vertebral arteries		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1318607	Atp11a	ATPase, class VI, type 11A	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:29539633
1318609	Enpp4	ectonucleotide pyrophosphatase/phosphodiesterase 4	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220519	MGI			
1318609	Enpp4	ectonucleotide pyrophosphatase/phosphodiesterase 4	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20201022	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20181227	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20250508	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20170105	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1318612	Galk2	galactokinase 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1318618	Swt1	SWT1 RNA endoribonuclease homolog (S. cerevisiae)	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1318618	Swt1	SWT1 RNA endoribonuclease homolog (S. cerevisiae)	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220519	MGI			
1318618	Swt1	SWT1 RNA endoribonuclease homolog (S. cerevisiae)	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1318618	Swt1	SWT1 RNA endoribonuclease homolog (S. cerevisiae)	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220519	MGI			
1318620	Rmdn3	regulator of microtubule dynamics 3	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:31501572
1318620	Rmdn3	regulator of microtubule dynamics 3	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1318622	Prkag3	protein kinase, AMP-activated, gamma 3 non-catalytic subunit	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247217
1318622	Prkag3	protein kinase, AMP-activated, gamma 3 non-catalytic subunit	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:15247217
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20161201	MGI			PMID:24739963
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20161201	MGI			PMID:24739963
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141204	MGI			PMID:23651732
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160114	MGI			
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20170105	MGI			
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160114	MGI			
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1318624	Izumo1r	IZUMO1 receptor, JUNO	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20170105	MGI			
1318627	Prpf39	pre-mRNA processing factor 39	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1318627	Prpf39	pre-mRNA processing factor 39	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230119	MGI			
1318627	Prpf39	pre-mRNA processing factor 39	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1318627	Prpf39	pre-mRNA processing factor 39	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1318627	Prpf39	pre-mRNA processing factor 39	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1318627	Prpf39	pre-mRNA processing factor 39	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1318627	Prpf39	pre-mRNA processing factor 39	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1318627	Prpf39	pre-mRNA processing factor 39	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1318627	Prpf39	pre-mRNA processing factor 39	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20230119	MGI			
1318629	Ift27	intraflagellar transport 27	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20151112	MGI			PMID:26023097
1318629	Ift27	intraflagellar transport 27	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20151112	MGI			PMID:26023097
1318629	Ift27	intraflagellar transport 27	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20151112	MGI			PMID:26023097
1318629	Ift27	intraflagellar transport 27	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0002243	abnormal vomeronasal organ morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20151112	MGI			PMID:26023097
1318629	Ift27	intraflagellar transport 27	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20151112	MGI			PMID:26023097
1318629	Ift27	intraflagellar transport 27	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0003950	abnormal plasma membrane morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0004159	double aortic arch		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0004182	abnormal spermiation		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0004880	lung cyst		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20151112	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20151112	MGI			PMID:26023097
1318629	Ift27	intraflagellar transport 27	gene	MP:0009837	abnormal sperm end piece morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20231221	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0010458	pulmonary trunk hypoplasia		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0010853	abnormal lung position or orientation		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151112	MGI			PMID:26023097
1318629	Ift27	intraflagellar transport 27	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0011250	abdominal situs ambiguus		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0011683	dual inferior vena cava		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0012285	misaligned sternebrae		IAGP		N	RGD:5509061	20150611	MGI			PMID:25446516
1318629	Ift27	intraflagellar transport 27	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20240613	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0031351	abnormal sperm flagellum thickness		IAGP		N	RGD:5509061	20220317	MGI			PMID:28964737
1318629	Ift27	intraflagellar transport 27	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:28964737
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0000731	increased collagen deposition in the muscles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24563484
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24563484
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20220519	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20220519	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24563484
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0004089	dilated sarcoplasmic reticulum		IAGP		N	RGD:5509061	20141003	MGI			PMID:24563484
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24563484
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20250508	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24563484
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:24563484
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:24563484
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24563484
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0013237	abnormal skeletal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23564457
1318631	Col6a3	collagen, type VI, alpha 3	gene	MP:0030803	abnormal tendon cell morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:24563484
1318633	Zfp592	zinc finger protein 592	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
1318633	Zfp592	zinc finger protein 592	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1318633	Zfp592	zinc finger protein 592	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1318633	Zfp592	zinc finger protein 592	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1318633	Zfp592	zinc finger protein 592	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1318636	Atp8b2	ATPase, class I, type 8B, member 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1318636	Atp8b2	ATPase, class I, type 8B, member 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1318636	Atp8b2	ATPase, class I, type 8B, member 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1318636	Atp8b2	ATPase, class I, type 8B, member 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318640	Tm4sf5	transmembrane 4 superfamily member 5	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20240523	MGI			
1318640	Tm4sf5	transmembrane 4 superfamily member 5	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:30956113
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17106887
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511315
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0000963	fused dorsal root ganglion		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0001067	absent mandibular nerve		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511315
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:17106887
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20181227	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511315
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511315
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17106887
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0003130	anal atresia		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511315
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0004175	telangiectasia		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17106887
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0004273	abnormal basal lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0005299	abnormal eye posterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17106887
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511315
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0005556	abnormal renal filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0005581	abnormal renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0005587	abnormal Meckel's cartilage morphology		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:17106887
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0008854	bleb		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511315
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0008856	fetal bleb		IAGP		N	RGD:5509061	20141003	MGI			PMID:17106887
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0009532	decreased parotid gland size		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0010526	aortic arch coarctation		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0010528	pulmonary vein hypoplasia		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511315
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0010912	herniated liver		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511315
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17106887
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011304	kidney papillary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011321	abnormal peritubular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011376	abnormal kidney corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011430	mesangiolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011437	glomerulus hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011455	absent glomerular endothelium fenestra		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011480	impaired ureteric peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011565	kidney papillary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460146
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011854	cerebral edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17106887
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011856	abnormal glomerular filtration barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011857	short kidney papilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:22488641
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011859	decreased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0011860	abnormal peritubular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19776720
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013814	abnormal hepatic portal vein connection		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013852	abnormal Mullerian duct topology		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013880	absent ductus venosus		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013932	fragmented Meckel's cartilage		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0014000	anastomosis between internal carotid artery and basilar artery		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0014006	absent posterior communicating artery		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0014087	retrolental blood		IEA		N	RGD:5509061	20180628	MGI			
1318642	Crim1	cysteine rich transmembrane BMP regulator 1	gene	MP:0031428	lens dislocation		IEA		N	RGD:5509061	20220714	MGI			
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23082185
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464903
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23082185
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493703
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21123569
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464903
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23082185
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464903
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493703
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173221
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464903
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464903
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464903
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464903
1318645	Guca1a	guanylate cyclase activator 1a (retina)	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464903
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190808	MGI			
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001714	absent trophoblast giant cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:20530197
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001714	absent trophoblast giant cells		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20530197
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0003708	binucleate		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20190808	MGI			
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0004266	pale placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861496
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20530197
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552834
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20530197
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20150305	MGI			PMID:19160489
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318647	Fzr1	fizzy and cell division cycle 20 related 1	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20530197
1318649	Trim36	tripartite motif-containing 36	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210729	MGI			PMID:32311190
1318649	Trim36	tripartite motif-containing 36	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240613	MGI			PMID:38697008
1318649	Trim36	tripartite motif-containing 36	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210729	MGI			PMID:32311190
1318652	Tasor	transcription activation suppressor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20150910	MGI			PMID:19099580
1318652	Tasor	transcription activation suppressor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20150910	MGI			PMID:24781204
1318652	Tasor	transcription activation suppressor	gene	MP:0009455	enhanced cued conditioning behavior		IEA		N	RGD:5509061	20260402	MGI			
1318652	Tasor	transcription activation suppressor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318652	Tasor	transcription activation suppressor	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20150910	MGI			PMID:24781204
1318652	Tasor	transcription activation suppressor	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318652	Tasor	transcription activation suppressor	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:24781204
1318654	Gart	phosphoribosylglycinamide formyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1318654	Gart	phosphoribosylglycinamide formyltransferase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1318654	Gart	phosphoribosylglycinamide formyltransferase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20181227	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20240328	MGI			PMID:37001993
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20160421	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20160421	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20240328	MGI			PMID:37001993
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20201022	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20180830	MGI			PMID:29084757
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20180830	MGI			PMID:29084757
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0002102	abnormal ear morphology		IEA		N	RGD:5509061	20160421	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20180830	MGI			PMID:29084757
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20260402	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20180830	MGI			PMID:29084757
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004413	absent cochlear microphonics		IAGP		N	RGD:5509061	20180830	MGI			PMID:29084757
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20180830	MGI			PMID:29084757
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20240328	MGI			PMID:29255404
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20240328	MGI			PMID:37001993
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20240328	MGI			PMID:29255404
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:37001993
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004517	decreased vestibular hair cell stereocilia number		IAGP		N	RGD:5509061	20240328	MGI			PMID:37001993
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:29255404
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20240328	MGI			PMID:29255404
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:29255404
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20180830	MGI			PMID:29084757
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20160421	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0011061	abnormal inner hair cell kinocilium morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:29255404
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20180830	MGI			PMID:29084757
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20240328	MGI			PMID:29255404
1318656	Cib2	calcium and integrin binding family member 2	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20240405	MGI			PMID:29255404
1318657	Ktn1	kinectin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11486041
1318658	Pxdn	peroxidasin	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20240523	MGI			
1318658	Pxdn	peroxidasin	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1318658	Pxdn	peroxidasin	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1318658	Pxdn	peroxidasin	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20200402	MGI			
1318658	Pxdn	peroxidasin	gene	MP:0002579	disorganized secondary lens fibers		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0005299	abnormal eye posterior chamber morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0006200	vitreous body deposition		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0009742	increased cornea stroma thickness		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0010235	abnormal retina inner limiting membrane morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0010709	absent eye anterior chamber		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0010713	corneal-lenticular stalk		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318658	Pxdn	peroxidasin	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0013743	ciliary body hypoplasia		IAGP		N	RGD:5509061	20150416	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1318658	Pxdn	peroxidasin	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:24895407
1318658	Pxdn	peroxidasin	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:24895407
1318660	Tspan32	tetraspanin 32	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20210826	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220811	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20210826	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210520	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210520	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0003883	enlarged stomach		IEA		N	RGD:5509061	20210826	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20260402	MGI			
1318660	Tspan32	tetraspanin 32	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077330
1318665	Dhx29	DExH-box helicase 29	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1318665	Dhx29	DExH-box helicase 29	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1318665	Dhx29	DExH-box helicase 29	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20181227	MGI			
1318665	Dhx29	DExH-box helicase 29	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1318665	Dhx29	DExH-box helicase 29	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20231207	MGI			
1318665	Dhx29	DExH-box helicase 29	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1318665	Dhx29	DExH-box helicase 29	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20111116	MGI			
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20150910	MGI			PMID:20022958
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150910	MGI			PMID:20022958
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055735
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:20022958
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20150910	MGI			PMID:20022958
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20150910	MGI			PMID:20022958
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20150910	MGI			PMID:20022958
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0009426	decreased soleus weight		IAGP		N	RGD:5509061	20150910	MGI			PMID:20022958
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0009428	decreased tibialis anterior weight		IAGP		N	RGD:5509061	20150910	MGI			PMID:20022958
1318671	Apobec2	apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20111116	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230119	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20230119	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230119	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393861
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393861
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393861
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0002648	delaminated enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393861
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0002649	abnormal enamel rod pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393861
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393861
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230119	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20230119	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20230119	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20240523	MGI			
1318676	Mmp20	matrix metallopeptidase 20 (enamelysin)	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20230119	MGI			
1318682	Plbd1	phospholipase B domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000324	increased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21668589
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000458	abnormal mandible morphology		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630138
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630138
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118178
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118178
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118178
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118178
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630138
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002465	abnormal eosinophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630138
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118178
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002802	abnormal discrimination learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118178
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118178
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118178
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630138
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630138
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0005270	abnormal zygomatic bone morphology		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20220519	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20211021	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118178
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21668589
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20211021	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20211021	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20210826	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0013520	increased CD4-positive NK T cell number		IEA		N	RGD:5509061	20211021	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0013523	increased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20211021	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20211021	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1318684	Spred1	sprouty protein with EVH-1 domain 1, related sequence	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20171019	MGI			PMID:15630138
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0001586	abnormal erythrocyte cell number		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141030	MGI			
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0002297	abnormal forced expiratory flow rates		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0002304	abnormal total lung capacity		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0002311	abnormal inspiratory capacity		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0002314	abnormal respiratory mechanics		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318686	Hmgn5	high-mobility group nucleosome binding domain 5	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1318688	Pias4	protein inhibitor of activated STAT 4	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528356
1318688	Pias4	protein inhibitor of activated STAT 4	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169916
1318688	Pias4	protein inhibitor of activated STAT 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169916
1318688	Pias4	protein inhibitor of activated STAT 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528356
1318691	Ctu1	cytosolic thiouridylase subunit 1	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20260402	MGI			
1318691	Ctu1	cytosolic thiouridylase subunit 1	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20260402	MGI			
1318691	Ctu1	cytosolic thiouridylase subunit 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1318691	Ctu1	cytosolic thiouridylase subunit 1	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1318691	Ctu1	cytosolic thiouridylase subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1318694	Ern2	endoplasmic reticulum to nucleus signalling 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238559
1318696	Dlx4	distal-less homeobox 4	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346937
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0000140	absent vertebral pedicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360776
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0000140	absent vertebral pedicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346937
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0000152	absent proximal rib		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360776
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360776
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360776
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360776
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0003939	abnormal myotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360776
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0004604	abnormal vertebral pedicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0004604	abnormal vertebral pedicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346937
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360776
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346937
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360776
1318698	Ripply2	ripply transcriptional repressor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531978
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15217369
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15978004
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855770
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15978004
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15978004
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15978004
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20230518	MGI			PMID:32086523
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611327
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22315402
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22315402
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22315402
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22315402
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15978004
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20220421	MGI			PMID:29329412
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0009085	abnormal uterine horn morphology		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20220421	MGI			PMID:29329412
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611327
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611327
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22315402
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220421	MGI			PMID:29329412
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611327
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15217369
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15978004
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0011122	absent primordial ovarian follicles		IAGP		N	RGD:5509061	20220421	MGI			PMID:18509161
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0013507	increased ovary apoptosis		IAGP		N	RGD:5509061	20220421	MGI			PMID:29329412
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0013607	ovary fibrosis		IAGP		N	RGD:5509061	20220421	MGI			PMID:29329412
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20220421	MGI			PMID:29329412
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:29329412
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:12855770
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:15217369
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:15978004
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:22315402
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20220421	MGI			PMID:29329412
1318701	Lhx8	LIM homeobox protein 8	gene	MP:0031020	premature ovarian failure		IAGP		N	RGD:5509061	20220421	MGI			PMID:29329412
1318703	Pum3	pumilio RNA-binding family member 3	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20260402	MGI			
1318703	Pum3	pumilio RNA-binding family member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745449
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745449
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0000947	convulsive seizures		IEA		N	RGD:5509061	20221110	MGI			
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0001136	dilated uterine cervix		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745449
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745449
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:24425853
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20221110	MGI			
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:24425853
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0005099	abnormal ciliary body morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:24425853
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20200521	MGI			PMID:24425853
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0005421	loose skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745449
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20221110	MGI			
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0005577	uterus prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745449
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0008418	abnormal cutaneous elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745449
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0010252	anterior subcapsular cataract		IAGP		N	RGD:5509061	20200521	MGI			PMID:24425853
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0010856	dilated respiratory conducting tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745449
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20221110	MGI			
1318706	Loxl1	lysyl oxidase-like 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20221110	MGI			
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20241121	MGI			
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0001785	edema		IEA		N	RGD:5509061	20241121	MGI			
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0002653	abnormal ependyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0003588	ureter stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241121	MGI			
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318708	Dlg5	discs large MAGUK scaffold protein 5	gene	MP:0011331	abnormal papillary duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765678
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518553
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518553
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518553
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518553
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518553
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518553
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518553
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518553
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0003619	abnormal urine color		IAGP		N	RGD:5509061	20141003	MGI			PMID:8188247
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20200528	MGI			PMID:31600782
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20200528	MGI			PMID:31600782
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20200528	MGI			PMID:31600782
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0013723	increased circulating tyrosine level		IAGP		N	RGD:5509061	20150409	MGI			PMID:10518553
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0030619	homogentisic aciduria		IAGP		N	RGD:5509061	20180906	MGI			PMID:8188247
1318714	Hgd	homogentisate 1, 2-dioxygenase	gene	MP:0030619	homogentisic aciduria		IAGP		N	RGD:5509061	20200528	MGI			PMID:31600782
1318716	Igsf11	immunoglobulin superfamily, member 11	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1318716	Igsf11	immunoglobulin superfamily, member 11	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20170601	MGI			PMID:26595655
1318716	Igsf11	immunoglobulin superfamily, member 11	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210520	MGI			
1318716	Igsf11	immunoglobulin superfamily, member 11	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20210520	MGI			
1318716	Igsf11	immunoglobulin superfamily, member 11	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1318716	Igsf11	immunoglobulin superfamily, member 11	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20170601	MGI			PMID:26595655
1318716	Igsf11	immunoglobulin superfamily, member 11	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0006411	upturned snout		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0011262	abnormal pharyngeal arch mesenchyme morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0012523	abnormal upper lip morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1318718	Mau2	MAU2 sister chromatid cohesion factor	gene	MP:0030065	face hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:24700590
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138077
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138077
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000608	dissociated hepatocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138077
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20230907	MGI			PMID:37219662
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20230907	MGI			PMID:37219662
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099835
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099835
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200402	MGI			
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11263494
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313485
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409406
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095756
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313485
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14630919
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099835
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11263494
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17409406
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099835
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002715	decreased glycogen catabolism rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138077
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002958	cerebral aqueductal stenosis		IAGP		N	RGD:5509061	20230907	MGI			PMID:37219662
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11263494
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313485
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099835
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138077
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20230907	MGI			PMID:37219662
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0008018	increased facial tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099835
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0008021	increased blastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099835
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20230907	MGI			PMID:37219662
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0009275	bruising		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099835
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11263494
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0010391	increased rhabdomyoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:16138077
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16138077
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099835
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313485
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11095756
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11263494
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20230907	MGI			PMID:37219662
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313485
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0012118	absent trophectoderm cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11313485
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0012119	increased trophectoderm apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11263494
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12450796
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0012690	abnormal stride length		IAGP		N	RGD:5509061	20160609	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:17409406
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:26363008
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0030973	impaired gluconeogenesis		IAGP		N	RGD:5509061	20191226	MGI			PMID:16138077
1318722	Smarcb1	SWI/SNF related BAF chromatin remodeling complex subunit B1	gene	MP:0031154	intestinal hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:12450796
1318723	Gprin1	G protein-regulated inducer of neurite outgrowth 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20240523	MGI			
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240718	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0021161	increased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318725	Cmtm3	CKLF-like MARVEL transmembrane domain containing 3	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20230817	MGI			PMID:37229825
1318727	Psph	phosphoserine phosphatase	gene	MP:0000104	abnormal sphenoid bone morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000141	abnormal vertebral body morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201231	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20201231	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000480	increased rib number		IEA		N	RGD:5509061	20160114	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000565	oligodactyly		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000613	abnormal salivary gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000614	absent salivary gland		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000618	small salivary gland		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000632	abnormal pineal gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000694	spleen hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000705	athymia		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000819	abnormal olfactory bulb morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000820	abnormal choroid plexus morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0001064	absent trochlear nerve		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318727	Psph	phosphoserine phosphatase	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002015	epithelioid cyst		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20201231	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002177	abnormal outer ear morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002199	abnormal brain commissure morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002237	abnormal nasal cavity morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002239	abnormal nasal septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002243	abnormal vomeronasal organ morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002249	abnormal larynx morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002428	abnormal semicircular canal morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20181227	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002858	abnormal posterior semicircular canal morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002928	abnormal bile duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003078	aphakia		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20160421	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003262	intestinal/bowel diverticulum		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003387	aorta coarctation		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003451	absent olfactory bulb		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20201231	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20220519	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318727	Psph	phosphoserine phosphatase	gene	MP:0004163	abnormal adenohypophysis morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004164	abnormal neurohypophysis morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004201	fetal growth retardation		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318727	Psph	phosphoserine phosphatase	gene	MP:0004266	pale placenta		IEA		N	RGD:5509061	20210520	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004539	absent maxilla		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004612	fusion of vertebral bodies		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0004666	absent stapedial artery		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318727	Psph	phosphoserine phosphatase	gene	MP:0005105	abnormal middle ear ossicle morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0005157	holoprosencephaly		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0005236	abnormal olfactory nerve morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20220519	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0006033	abnormal external auditory canal morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0006254	thin cerebral cortex		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0008128	abnormal brain internal capsule morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0008129	absent brain internal capsule		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318727	Psph	phosphoserine phosphatase	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0009688	abnormal spinal cord central canal morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0009707	absent external auditory canal		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0009771	absent optic chiasm		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0009904	tongue hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0009905	absent tongue		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0010912	herniated liver		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318727	Psph	phosphoserine phosphatase	gene	MP:0012303	umbilical vein stenosis		IEA		N	RGD:5509061	20180628	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013247	placenta necrosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318727	Psph	phosphoserine phosphatase	gene	MP:0013362	absent pineal gland		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013595	absent vomeronasal organ		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013818	abnormal oral cavity morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013833	absent olfactory nerve		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318727	Psph	phosphoserine phosphatase	gene	MP:0013849	absent abducens nerve		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013850	absent posterior commissure		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013855	absent celiac artery		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013875	increased trigeminal neuroma incidence		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013878	abnormal ductus venosus valve topology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013926	absent neurohypophysis		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013927	abnormal facial nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013929	absent eye muscles		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013932	fragmented Meckel's cartilage		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013933	short Meckel's cartilage		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013935	basal brain tissue herniation		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013936	abnormal thymus topology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013948	intraembryonal intestine elongation		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013950	abnormal dorsal root ganglion topology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013980	abnormal pulmonary artery origin		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013988	absent portal vein segment		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013994	abnormal parasellar internal carotid artery branch morphology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0013996	abnormal vertebral artery origin		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0014009	anastomosis between middle cerebral arteries		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0014019	embryo cyst		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0014022	abnormal duodenum topology		IEA		N	RGD:5509061	20170504	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1318727	Psph	phosphoserine phosphatase	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:29539633
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505825
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318729	Sox12	SRY (sex determining region Y)-box 12	gene	MP:0011261	abnormal limb mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1318731	Irf9	interferon regulatory factor 9	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12923053
1318731	Irf9	interferon regulatory factor 9	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114377
1318731	Irf9	interferon regulatory factor 9	gene	MP:0002418	increased susceptibility to viral infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9078371
1318731	Irf9	interferon regulatory factor 9	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070172
1318731	Irf9	interferon regulatory factor 9	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800576
1318731	Irf9	interferon regulatory factor 9	gene	MP:0008575	increased circulating interferon-beta level		IEA		N	RGD:5509061	20161201	MGI			
1318731	Irf9	interferon regulatory factor 9	gene	MP:0012556	increased cell death		IEA		N	RGD:5509061	20161201	MGI			
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0013704	increased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:22422825
1318733	Dhx36	DEAH-box helicase 36	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:22422825
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000548	long limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675086
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16117793
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675086
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675086
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8751968
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675085
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675085
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675086
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837020
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837020
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531021
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16117793
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531021
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0002879	increased cellular sensitivity to X-ray irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11960916
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675086
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10383746
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531021
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004143	muscle hypertonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675086
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21151170
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675085
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531021
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675085
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0005362	abnormal Langerhans cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8751968
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11960916
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10383746
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675085
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20190829	MGI			PMID:8751968
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0009387	abnormal epidermal pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16117793
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531021
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675085
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0009814	increased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10651981
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0010289	increased urinary system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21151170
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531021
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16117793
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20150611	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0010699	dilated hair follicle		IAGP		N	RGD:5509061	20181129	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10383746
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7675086
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18790090
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12531021
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0013551	decreased cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20161201	MGI			PMID:11687625
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0014762	impaired base-excision repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:17326724
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0014762	impaired base-excision repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:7675085
1318736	Xpa	xeroderma pigmentosum, complementation group A	gene	MP:0030003	hippocampus atrophy		IAGP		N	RGD:5509061	20170706	MGI			PMID:22174697
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191128	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0002582	disorganized extraembryonic tissue		IEA		N	RGD:5509061	20191128	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20160811	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20160804	MGI			
1318738	Mrps25	mitochondrial ribosomal protein S25	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318741	Vwa8	von Willebrand factor A domain containing 8	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1318741	Vwa8	von Willebrand factor A domain containing 8	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1318741	Vwa8	von Willebrand factor A domain containing 8	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1318741	Vwa8	von Willebrand factor A domain containing 8	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20160421	MGI			
1318741	Vwa8	von Willebrand factor A domain containing 8	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1318741	Vwa8	von Willebrand factor A domain containing 8	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0000495	abnormal colon morphology		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23569244
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0002581	abnormal ileum morphology		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20250508	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0005005	abnormal self tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23569244
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23569244
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23569244
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23569244
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540904
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23569244
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23569244
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0013520	increased CD4-positive NK T cell number		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0013523	increased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0013763	increased T-helper cell number		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20230601	MGI			
1318742	Psmb11	proteasome (prosome, macropain) subunit, beta type, 11	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20230601	MGI			
1318743	Slc25a40	solute carrier family 25, member 40	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18799693
1318744	4921536K21Rik	RIKEN cDNA 4921536K21 gene	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1318744	4921536K21Rik	RIKEN cDNA 4921536K21 gene	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20180315	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20180315	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20180315	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20180315	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0006205	embryonic lethality between implantation and somite formation		IAGP		N	RGD:5509061	20180315	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180315	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:27040500
1318749	Upf3a	UPF3 regulator of nonsense transcripts homolog A (yeast)	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:27040500
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0000794	abnormal parietal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20241121	MGI			
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0004631	abnormal auditory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1318752	Arhgap33	Rho GTPase activating protein 33	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318754	Septin4	septin 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737930
1318754	Septin4	septin 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737930
1318754	Septin4	septin 4	gene	MP:0003666	impaired sperm capacitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737930
1318754	Septin4	septin 4	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737930
1318754	Septin4	septin 4	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0009242	thin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0009835	absent sperm annulus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737930
1318754	Septin4	septin 4	gene	MP:0009835	absent sperm annulus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:15737931
1318754	Septin4	septin 4	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:15737930
1318754	Septin4	septin 4	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:15737931
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20250508	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210128	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20210826	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20250508	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210520	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20241121	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20201022	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0009303	decreased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210520	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210520	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651815
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0012134	absent umbilical cord		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0012301	absent umbilical cord blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1318757	Tnks	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	gene	MP:0030021	increased muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:19651815
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0000955	abnormal spinal cord morphology		IEA		N	RGD:5509061	20170105	MGI			
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24312227
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24312227
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:24312227
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:24312227
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0002916	increased synaptic depression		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:24312227
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20151217	MGI			PMID:25047565
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1318760	Elfn1	leucine rich repeat and fibronectin type III, extracellular 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25047565
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0000678	abnormal parathyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0003395	abnormal subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0003955	abnormal ultimobranchial body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0006339	abnormal third pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0006340	abnormal fourth pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20180614	MGI			PMID:25053427
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0010356	abnormal second pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0010395	abnormal pharyngeal arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0010564	abnormal fetal ductus arteriosus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053427
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0030335	absent third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0030340	absent fourth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:21177346
1318762	Ripply3	ripply transcriptional repressor 3	gene	MP:0030589	increased pancreatic alpha cell mass		IAGP		N	RGD:5509061	20180614	MGI			PMID:25053427
1318764	Jph1	junctophilin 1	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535622
1318764	Jph1	junctophilin 1	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535622
1318764	Jph1	junctophilin 1	gene	MP:0009411	abnormal skeletal muscle fiber triad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535622
1318764	Jph1	junctophilin 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535622
1318764	Jph1	junctophilin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535622
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817531
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146193
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19491376
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817531
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19491376
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817531
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817531
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19491376
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146193
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19491376
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146193
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19491376
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817531
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146193
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146193
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146193
1318767	Smc1b	structural maintenance of chromosomes 1B	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19491376
1318771	Ddx4	DEAD box helicase 4	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1318771	Ddx4	DEAD box helicase 4	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
1318771	Ddx4	DEAD box helicase 4	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10766740
1318771	Ddx4	DEAD box helicase 4	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
1318771	Ddx4	DEAD box helicase 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20251023	MGI			PMID:27718356
1318771	Ddx4	DEAD box helicase 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10766740
1318771	Ddx4	DEAD box helicase 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
1318771	Ddx4	DEAD box helicase 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20251023	MGI			PMID:27718356
1318771	Ddx4	DEAD box helicase 4	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
1318771	Ddx4	DEAD box helicase 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20251023	MGI			PMID:27718356
1318771	Ddx4	DEAD box helicase 4	gene	MP:0002982	abnormal primordial germ cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10766740
1318771	Ddx4	DEAD box helicase 4	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10766740
1318771	Ddx4	DEAD box helicase 4	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23858447
1318771	Ddx4	DEAD box helicase 4	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20251023	MGI			PMID:31839538
1318771	Ddx4	DEAD box helicase 4	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1318771	Ddx4	DEAD box helicase 4	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20251023	MGI			PMID:31839538
1318771	Ddx4	DEAD box helicase 4	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10766740
1318771	Ddx4	DEAD box helicase 4	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17038506
1318771	Ddx4	DEAD box helicase 4	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10766740
1318771	Ddx4	DEAD box helicase 4	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20251023	MGI			PMID:31839538
1318771	Ddx4	DEAD box helicase 4	gene	MP:0008967	absent chiasmata formation		IAGP		N	RGD:5509061	20251023	MGI			PMID:31839538
1318771	Ddx4	DEAD box helicase 4	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:31839538
1318771	Ddx4	DEAD box helicase 4	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20251023	MGI			PMID:31839538
1318771	Ddx4	DEAD box helicase 4	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:10766740
1318771	Ddx4	DEAD box helicase 4	gene	MP:0030934	decreased primordial germ cell proliferation		IAGP		N	RGD:5509061	20190411	MGI			PMID:10766740
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20231207	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000423	delayed hair regrowth		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18815260
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18815260
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002991	abnormal sebaceous gland physiology		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230119	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18815260
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18815260
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18815260
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0009794	sebaceous gland hyperplasia		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0010137	delayed exit from anagen phase		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0013378	increased sebocyte number		IAGP		N	RGD:5509061	20150813	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0020380	abnormal galactolipid level		IAGP		N	RGD:5509061	20190815	MGI			PMID:21491498
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0030571	dilated piliary canal		IAGP		N	RGD:5509061	20180524	MGI			PMID:21628453
1318773	Fa2h	fatty acid 2-hydroxylase	gene	MP:0030923	abnormal hair follicle ostium morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:21628453
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0009608	abnormal epidermal lamellar body morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0013391	abnormal Meibomian gland physiology		IAGP		N	RGD:5509061	20221117	MGI			PMID:34113821
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0013530	abnormal periderm morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0020583	decreased ceramide level		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318775	Cyp4f39	cytochrome P450, family 4, subfamily f, polypeptide 39	gene	MP:0030605	abnormal corneocyte morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31356814
1318776	Ccdc33	coiled-coil domain containing 33	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20160114	MGI			
1318776	Ccdc33	coiled-coil domain containing 33	gene	MP:0005630	increased lung weight		IEA		N	RGD:5509061	20241121	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230119	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20230119	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230119	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20240523	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230119	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230119	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230119	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1318778	Gzf1	GDNF-inducible zinc finger protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0000316	cellular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732874
1318781	Csk	c-src tyrosine kinase	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732874
1318781	Csk	c-src tyrosine kinase	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348736
1318781	Csk	c-src tyrosine kinase	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348736
1318781	Csk	c-src tyrosine kinase	gene	MP:0001432	abnormal food preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348736
1318781	Csk	c-src tyrosine kinase	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348736
1318781	Csk	c-src tyrosine kinase	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975240
1318781	Csk	c-src tyrosine kinase	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20210520	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20190502	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346773
1318781	Csk	c-src tyrosine kinase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20346773
1318781	Csk	c-src tyrosine kinase	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975240
1318781	Csk	c-src tyrosine kinase	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975240
1318781	Csk	c-src tyrosine kinase	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20190502	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975240
1318781	Csk	c-src tyrosine kinase	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732874
1318781	Csk	c-src tyrosine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7685657
1318781	Csk	c-src tyrosine kinase	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1318781	Csk	c-src tyrosine kinase	gene	MP:0012170	absent optic placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8513497
1318781	Csk	c-src tyrosine kinase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318783	Nek11	NIMA (never in mitosis gene a)-related expressed kinase 11	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1318783	Nek11	NIMA (never in mitosis gene a)-related expressed kinase 11	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1318783	Nek11	NIMA (never in mitosis gene a)-related expressed kinase 11	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0008876	decreased uterine NK cell number		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0009094	abnormal endometrial gland morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0009251	enlarged endometrial glands		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318788	Pgrmc2	progesterone receptor membrane component 2	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20180315	MGI			PMID:28005395
1318792	Mon2	MON2 homolog, regulator of endosome to Golgi trafficking	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1318792	Mon2	MON2 homolog, regulator of endosome to Golgi trafficking	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1318792	Mon2	MON2 homolog, regulator of endosome to Golgi trafficking	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1318792	Mon2	MON2 homolog, regulator of endosome to Golgi trafficking	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318792	Mon2	MON2 homolog, regulator of endosome to Golgi trafficking	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1318794	Btg4	BTG anti-proliferation factor 4	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20250220	MGI			PMID:27065194
1318794	Btg4	BTG anti-proliferation factor 4	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20250220	MGI			PMID:27065194
1318794	Btg4	BTG anti-proliferation factor 4	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20250220	MGI			PMID:27065194
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0001599	abnormal blood volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14642567
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14642567
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101838
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914751
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101838
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14642567
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242442
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242442
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101838
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101838
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242442
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14642567
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14642567
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:14642567
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242442
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242442
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914751
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14642567
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808625
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101838
1318796	Blm	Bloom syndrome, RecQ like helicase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14642567
1318799	Mfhas1	malignant fibrous histiocytoma amplified sequence 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20250508	MGI			
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0004512	anosmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:18032602
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0030962	abnormal inner hair cell kinocilium location or orientation		IAGP		N	RGD:5509061	20190725	MGI			PMID:16170314
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:15772095
1318802	Mkks	McKusick-Kaufman syndrome	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:16170314
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20190502	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20210520	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20190502	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20190502	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IEA		N	RGD:5509061	20220519	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20190502	MGI			
1318804	Alg6	ALG6 alpha-1,3-glucosyltransferase	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1318805	Cnep1r1	CTD nuclear envelope phosphatase 1 regulatory subunit 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1318805	Cnep1r1	CTD nuclear envelope phosphatase 1 regulatory subunit 1	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20210128	MGI			
1318805	Cnep1r1	CTD nuclear envelope phosphatase 1 regulatory subunit 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1318805	Cnep1r1	CTD nuclear envelope phosphatase 1 regulatory subunit 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1318805	Cnep1r1	CTD nuclear envelope phosphatase 1 regulatory subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1318805	Cnep1r1	CTD nuclear envelope phosphatase 1 regulatory subunit 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20230601	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0005270	abnormal zygomatic bone morphology		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20260402	MGI			
1318810	Brat1	BRCA1-associated ATM activator 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1318820	Psmc6	proteasome (prosome, macropain) 26S subunit, ATPase, 6	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1318820	Psmc6	proteasome (prosome, macropain) 26S subunit, ATPase, 6	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1318820	Psmc6	proteasome (prosome, macropain) 26S subunit, ATPase, 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318820	Psmc6	proteasome (prosome, macropain) 26S subunit, ATPase, 6	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1318820	Psmc6	proteasome (prosome, macropain) 26S subunit, ATPase, 6	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210520	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20201022	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20181227	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20170105	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20170105	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20221215	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20161201	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307874
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20141003	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20170105	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20160811	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20141003	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20141003	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0002544	brachydactyly		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20141003	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307874
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0003189	fused joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307874
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20211021	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20221215	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20221215	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20221215	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20221215	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20240523	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0011952	decreased cardiac stroke volume		IEA		N	RGD:5509061	20210128	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0011999	abnormal tail length		IEA		N	RGD:5509061	20201022	MGI			
1318822	Dnase1l2	deoxyribonuclease 1-like 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1318824	Sephs2	selenophosphate synthetase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318824	Sephs2	selenophosphate synthetase 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854167
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20250508	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854167
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20260402	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854167
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0002931	glutaricadicuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854167
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854167
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20220519	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20250508	MGI			
1318827	Gcdh	glutaryl-Coenzyme A dehydrogenase	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20190103	MGI			PMID:28545977
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20211021	MGI			
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210128	MGI			
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0005451	abnormal body composition		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0009130	increased white fat cell number		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318830	Creb3	cAMP responsive element binding protein 3	gene	MP:0031414	decreased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20240328	MGI			PMID:35637262
1318832	Mbd3l2	methyl-CpG binding domain protein 3-like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18942147
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000519	hydronephrosis		IEA		N	RGD:5509061	20170209	MGI			
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20170209	MGI			
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20170209	MGI			
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0004407	increased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0006198	enophthalmos		IEA		N	RGD:5509061	20170209	MGI			
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0006286	inner ear hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0011666	double outlet right ventricle, ventricular defect committed to aorta		IEA		N	RGD:5509061	20170209	MGI			
1318834	Dvl3	dishevelled segment polarity protein 3	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1318836	Gpc5	glypican 5	gene	MP:0002924	delayed CNS synapse formation		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0020512	abnormal dendritic mushroom spine morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0020514	abnormal dendritic thin spine morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318836	Gpc5	glypican 5	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:40048429
1318840	Cldn6	claudin 6	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318840	Cldn6	claudin 6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318840	Cldn6	claudin 6	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318840	Cldn6	claudin 6	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1318840	Cldn6	claudin 6	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318840	Cldn6	claudin 6	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318840	Cldn6	claudin 6	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318840	Cldn6	claudin 6	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318840	Cldn6	claudin 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318840	Cldn6	claudin 6	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318840	Cldn6	claudin 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22900086
1318842	Krt23	keratin 23	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828515
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828515
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20240523	MGI			
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828515
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828515
1318844	Tmeff2	transmembrane protein with EGF-like and two follistatin-like domains 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20190502	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20201022	MGI			
1318846	Man2b2	mannosidase 2, alpha B2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747814
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213437
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747814
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213437
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747814
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213437
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213437
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747814
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0004273	abnormal basal lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747814
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0004360	absent ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213437
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213437
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747814
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213437
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11747814
1318852	Reck	reversion-inducing-cysteine-rich protein with kazal motifs	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20691046
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20161027	MGI			PMID:24696448
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20161027	MGI			PMID:24696448
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20161027	MGI			PMID:24696448
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20161027	MGI			PMID:24696448
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0002869	increased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20161027	MGI			PMID:24696448
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20161027	MGI			PMID:24696448
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20161027	MGI			PMID:24696448
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20161027	MGI			PMID:24696448
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0008136	enlarged Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150927
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809356
1318854	Irak3	interleukin-1 receptor-associated kinase 3	gene	MP:0013772	increased effector memory T-helper cell number		IAGP		N	RGD:5509061	20161027	MGI			PMID:24696448
1318856	Ogfod1	2-oxoglutarate and iron-dependent oxygenase domain containing 1	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20160804	MGI			
1318856	Ogfod1	2-oxoglutarate and iron-dependent oxygenase domain containing 1	gene	MP:0001191	abnormal skin condition		IEA		N	RGD:5509061	20160804	MGI			
1318856	Ogfod1	2-oxoglutarate and iron-dependent oxygenase domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150101	MGI			PMID:24550447
1318856	Ogfod1	2-oxoglutarate and iron-dependent oxygenase domain containing 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20160804	MGI			
1318858	Rdh5	retinol dehydrogenase 5	gene	MP:0003011	delayed dark adaptation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907141
1318858	Rdh5	retinol dehydrogenase 5	gene	MP:0003011	delayed dark adaptation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634683
1318858	Rdh5	retinol dehydrogenase 5	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907141
1318858	Rdh5	retinol dehydrogenase 5	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634683
1318859	Tmem72	transmembrane protein 72	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1318859	Tmem72	transmembrane protein 72	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20190808	MGI			
1318859	Tmem72	transmembrane protein 72	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1318859	Tmem72	transmembrane protein 72	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210826	MGI			
1318859	Tmem72	transmembrane protein 72	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20190808	MGI			
1318859	Tmem72	transmembrane protein 72	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1318859	Tmem72	transmembrane protein 72	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20190808	MGI			
1318859	Tmem72	transmembrane protein 72	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1318859	Tmem72	transmembrane protein 72	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210826	MGI			
1318859	Tmem72	transmembrane protein 72	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20190808	MGI			
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0002708	nephrolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0005360	urolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20201210	MGI			PMID:31821850
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20201210	MGI			PMID:31821850
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0009646	urinary bladder inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0011517	hyperoxaluria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22189945
1318861	Grhpr	glyoxylate reductase/hydroxypyruvate reductase	gene	MP:0011517	hyperoxaluria		IAGP		N	RGD:5509061	20201210	MGI			PMID:31821850
1318863	Usp3	ubiquitin specific peptidase 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0002208	abnormal germ cell morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318866	Thumpd1	THUMP domain containing 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1318870	Rnf144b	ring finger protein 144B	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20160421	MGI			
1318870	Rnf144b	ring finger protein 144B	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20160421	MGI			
1318870	Rnf144b	ring finger protein 144B	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1318870	Rnf144b	ring finger protein 144B	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20241226	MGI			PMID:39285245
1318870	Rnf144b	ring finger protein 144B	gene	MP:0020938	decreased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20241226	MGI			PMID:39285245
1318870	Rnf144b	ring finger protein 144B	gene	MP:0031039	decreased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20241226	MGI			PMID:39285245
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20160811	MGI			
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20160811	MGI			
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563261
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20251225	MGI			PMID:38078859
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563261
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10648608
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0002497	increased IgE level		IEA		N	RGD:5509061	20180215	MGI			
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563261
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563261
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563261
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0008233	abnormal pro-B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563261
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0008657	increased interleukin-1 beta secretion		IEA		N	RGD:5509061	20180215	MGI			
1318875	Blk	Blk proto-oncogene, Src family tyrosine kinase	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20251225	MGI			PMID:38078859
1318879	Sec62	SEC62 homolog, preprotein translocation	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1318879	Sec62	SEC62 homolog, preprotein translocation	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1318879	Sec62	SEC62 homolog, preprotein translocation	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1318879	Sec62	SEC62 homolog, preprotein translocation	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1318883	Fus	fused in sarcoma	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20171228	MGI			PMID:29053787
1318883	Fus	fused in sarcoma	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20171228	MGI			PMID:29053787
1318883	Fus	fused in sarcoma	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:26842965
1318883	Fus	fused in sarcoma	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:29053787
1318883	Fus	fused in sarcoma	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20171228	MGI			PMID:29053787
1318883	Fus	fused in sarcoma	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20171228	MGI			PMID:29053787
1318883	Fus	fused in sarcoma	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1318883	Fus	fused in sarcoma	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20171228	MGI			PMID:29053787
1318883	Fus	fused in sarcoma	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170223	MGI			PMID:26842965
1318883	Fus	fused in sarcoma	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20160421	MGI			
1318883	Fus	fused in sarcoma	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15797031
1318883	Fus	fused in sarcoma	gene	MP:0010378	increased respiratory quotient		IEA		N	RGD:5509061	20210128	MGI			
1318883	Fus	fused in sarcoma	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654943
1318883	Fus	fused in sarcoma	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655065
1318883	Fus	fused in sarcoma	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170223	MGI			PMID:26842965
1318883	Fus	fused in sarcoma	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1318885	Gpatch2	G patch domain containing 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20230817	MGI			PMID:36973252
1318887	Map7	microtubule-associated protein 7	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837026
1318887	Map7	microtubule-associated protein 7	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20150122	MGI			PMID:19329343
1318887	Map7	microtubule-associated protein 7	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837026
1318887	Map7	microtubule-associated protein 7	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875885
1318887	Map7	microtubule-associated protein 7	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837026
1318887	Map7	microtubule-associated protein 7	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20150122	MGI			PMID:19329343
1318887	Map7	microtubule-associated protein 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837026
1318887	Map7	microtubule-associated protein 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875885
1318887	Map7	microtubule-associated protein 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20150122	MGI			PMID:19329343
1318887	Map7	microtubule-associated protein 7	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837026
1318887	Map7	microtubule-associated protein 7	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20250508	MGI			
1318887	Map7	microtubule-associated protein 7	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837026
1318887	Map7	microtubule-associated protein 7	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875885
1318887	Map7	microtubule-associated protein 7	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:19329343
1318887	Map7	microtubule-associated protein 7	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837026
1318887	Map7	microtubule-associated protein 7	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1318887	Map7	microtubule-associated protein 7	gene	MP:0004085	abnormal heartbeat		IEA		N	RGD:5509061	20250508	MGI			
1318887	Map7	microtubule-associated protein 7	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20250508	MGI			
1318887	Map7	microtubule-associated protein 7	gene	MP:0004752	decreased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875885
1318887	Map7	microtubule-associated protein 7	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20150122	MGI			PMID:19329343
1318887	Map7	microtubule-associated protein 7	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20150122	MGI			PMID:19329343
1318887	Map7	microtubule-associated protein 7	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837026
1318887	Map7	microtubule-associated protein 7	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837026
1318887	Map7	microtubule-associated protein 7	gene	MP:0006428	ectopic Sertoli cells		IAGP		N	RGD:5509061	20160915	MGI			PMID:8875885
1318887	Map7	microtubule-associated protein 7	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875885
1318887	Map7	microtubule-associated protein 7	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1318887	Map7	microtubule-associated protein 7	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875885
1318889	Arpc5l	actin related protein 2/3 complex, subunit 5-like	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20201022	MGI			
1318889	Arpc5l	actin related protein 2/3 complex, subunit 5-like	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1318889	Arpc5l	actin related protein 2/3 complex, subunit 5-like	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1318889	Arpc5l	actin related protein 2/3 complex, subunit 5-like	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0000452	abnormal mouth morphology		IEA		N	RGD:5509061	20210128	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20210826	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20230601	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20200402	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20200402	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20191114	MGI			PMID:30704515
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20200402	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20191114	MGI			PMID:30704515
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0009130	increased white fat cell number		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318898	Apmap	adipocyte plasma membrane associated protein	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20191114	MGI			PMID:28559441
1318901	Trmt6	tRNA methyltransferase 6	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1318901	Trmt6	tRNA methyltransferase 6	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1318903	Amdhd1	amidohydrolase domain containing 1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1318907	Sult2b1	sulfotransferase family, cytosolic, 2B, member 1	gene	MP:0003947	abnormal cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1318910	Mcoln2	mucolipin 2	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20170803	MGI			PMID:26432893
1318910	Mcoln2	mucolipin 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20170803	MGI			PMID:26432893
1318910	Mcoln2	mucolipin 2	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20170803	MGI			PMID:26432893
1318910	Mcoln2	mucolipin 2	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20170803	MGI			PMID:26432893
1318910	Mcoln2	mucolipin 2	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20170803	MGI			PMID:26432893
1318912	Trim41	tripartite motif-containing 41	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20240912	MGI			PMID:35648791
1318912	Trim41	tripartite motif-containing 41	gene	MP:0014436	decreased interferon level		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0014438	decreased interleukin level		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318912	Trim41	tripartite motif-containing 41	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240829	MGI			PMID:33640899
1318915	Osbpl6	oxysterol binding protein-like 6	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1318915	Osbpl6	oxysterol binding protein-like 6	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20260402	MGI			
1318915	Osbpl6	oxysterol binding protein-like 6	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1318915	Osbpl6	oxysterol binding protein-like 6	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20250508	MGI			
1318917	Dhx30	DExH-box helicase 30	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1318917	Dhx30	DExH-box helicase 30	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1318917	Dhx30	DExH-box helicase 30	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20211021	MGI			
1318917	Dhx30	DExH-box helicase 30	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25219788
1318917	Dhx30	DExH-box helicase 30	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160225	MGI			PMID:25219788
1318917	Dhx30	DExH-box helicase 30	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20160225	MGI			PMID:25219788
1318917	Dhx30	DExH-box helicase 30	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1318917	Dhx30	DExH-box helicase 30	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1318917	Dhx30	DExH-box helicase 30	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20160225	MGI			PMID:25219788
1318917	Dhx30	DExH-box helicase 30	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160225	MGI			PMID:25219788
1318917	Dhx30	DExH-box helicase 30	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318917	Dhx30	DExH-box helicase 30	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1318917	Dhx30	DExH-box helicase 30	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1318919	Lama2	laminin, alpha 2	gene	MP:0000032	cochlear degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17459142
1318919	Lama2	laminin, alpha 2	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:17459142
1318919	Lama2	laminin, alpha 2	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792494
1318919	Lama2	laminin, alpha 2	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1318919	Lama2	laminin, alpha 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876525
1318919	Lama2	laminin, alpha 2	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876525
1318919	Lama2	laminin, alpha 2	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10616210
1318919	Lama2	laminin, alpha 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876525
1318919	Lama2	laminin, alpha 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:5434356
1318919	Lama2	laminin, alpha 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710454
1318919	Lama2	laminin, alpha 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876525
1318919	Lama2	laminin, alpha 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:5434356
1318919	Lama2	laminin, alpha 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710454
1318919	Lama2	laminin, alpha 2	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1318919	Lama2	laminin, alpha 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:4120487
1318919	Lama2	laminin, alpha 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:6831246
1318919	Lama2	laminin, alpha 2	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6831246
1318919	Lama2	laminin, alpha 2	gene	MP:0001107	decreased Schwann cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1318919	Lama2	laminin, alpha 2	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127160
1318919	Lama2	laminin, alpha 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1301630
1318919	Lama2	laminin, alpha 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
1318919	Lama2	laminin, alpha 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:2989438
1318919	Lama2	laminin, alpha 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710454
1318919	Lama2	laminin, alpha 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
1318919	Lama2	laminin, alpha 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1318919	Lama2	laminin, alpha 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876525
1318919	Lama2	laminin, alpha 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710454
1318919	Lama2	laminin, alpha 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15823249
1318919	Lama2	laminin, alpha 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1318919	Lama2	laminin, alpha 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:5434356
1318919	Lama2	laminin, alpha 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710454
1318919	Lama2	laminin, alpha 2	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1301630
1318919	Lama2	laminin, alpha 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2989438
1318919	Lama2	laminin, alpha 2	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
1318919	Lama2	laminin, alpha 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1318919	Lama2	laminin, alpha 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876525
1318919	Lama2	laminin, alpha 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710454
1318919	Lama2	laminin, alpha 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1318919	Lama2	laminin, alpha 2	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
1318919	Lama2	laminin, alpha 2	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:2989438
1318919	Lama2	laminin, alpha 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127160
1318919	Lama2	laminin, alpha 2	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0002880	opisthotonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:5434356
1318919	Lama2	laminin, alpha 2	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15823249
1318919	Lama2	laminin, alpha 2	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
1318919	Lama2	laminin, alpha 2	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
1318919	Lama2	laminin, alpha 2	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792494
1318919	Lama2	laminin, alpha 2	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
1318919	Lama2	laminin, alpha 2	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2989438
1318919	Lama2	laminin, alpha 2	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12044978
1318919	Lama2	laminin, alpha 2	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1161034
1318919	Lama2	laminin, alpha 2	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127160
1318919	Lama2	laminin, alpha 2	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:894325
1318919	Lama2	laminin, alpha 2	gene	MP:0004273	abnormal basal lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1318919	Lama2	laminin, alpha 2	gene	MP:0004273	abnormal basal lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0004273	abnormal basal lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344408
1318919	Lama2	laminin, alpha 2	gene	MP:0004289	abnormal bony labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0004300	abnormal organ of Corti supporting cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0004325	absent vestibular hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0004363	stria vascularis degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0004405	absent cochlear hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876525
1318919	Lama2	laminin, alpha 2	gene	MP:0004716	abnormal cochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:61889
1318919	Lama2	laminin, alpha 2	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15578095
1318919	Lama2	laminin, alpha 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1301630
1318919	Lama2	laminin, alpha 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792494
1318919	Lama2	laminin, alpha 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792494
1318919	Lama2	laminin, alpha 2	gene	MP:0005124	increased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1301630
1318919	Lama2	laminin, alpha 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710454
1318919	Lama2	laminin, alpha 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1318919	Lama2	laminin, alpha 2	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:630405
1318919	Lama2	laminin, alpha 2	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
1318919	Lama2	laminin, alpha 2	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9326364
1318919	Lama2	laminin, alpha 2	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589799
1318919	Lama2	laminin, alpha 2	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
1318919	Lama2	laminin, alpha 2	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
1318919	Lama2	laminin, alpha 2	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3440862
1318919	Lama2	laminin, alpha 2	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792494
1318919	Lama2	laminin, alpha 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1318919	Lama2	laminin, alpha 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1318919	Lama2	laminin, alpha 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710454
1318919	Lama2	laminin, alpha 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876525
1318919	Lama2	laminin, alpha 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126936
1318919	Lama2	laminin, alpha 2	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:10616210
1318919	Lama2	laminin, alpha 2	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:15578095
1318919	Lama2	laminin, alpha 2	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:16127160
1318919	Lama2	laminin, alpha 2	gene	MP:0020380	abnormal galactolipid level		IAGP		N	RGD:5509061	20190815	MGI			PMID:2989438
1318919	Lama2	laminin, alpha 2	gene	MP:0020452	abnormal axon radial sorting		IAGP		N	RGD:5509061	20170914	MGI			PMID:15699217
1318919	Lama2	laminin, alpha 2	gene	MP:0030798	joint contracture		IAGP		N	RGD:5509061	20181122	MGI			PMID:12609503
1318919	Lama2	laminin, alpha 2	gene	MP:0030979	decreased spinal cord weight		IAGP		N	RGD:5509061	20191010	MGI			PMID:2989438
1318919	Lama2	laminin, alpha 2	gene	MP:0031204	hindlimb paresis		IAGP		N	RGD:5509061	20210218	MGI			PMID:18430779
1318919	Lama2	laminin, alpha 2	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:18430779
1318920	Ift70a1	intraflagellar transport 70A1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20260402	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20231207	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318924	Dcun1d3	defective in cullin neddylation 1 domain containing 3	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797173
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017726
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:647395
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7472477
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:647395
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7472477
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001108	absent Schwann cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:647395
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7472477
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003381	vitreal fibroplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20111116	MGI			
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0004220	abnormal peripheral nervous system regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7472477
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20220512	MGI			PMID:34142127
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797173
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017726
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0006200	vitreous body deposition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0008509	disorganized retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0008520	disorganized retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20250403	MGI			PMID:939913
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009415	skeletal muscle degeneration		IEA		N	RGD:5509061	20111116	MGI			
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7506762
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111892
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20250911	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0014742	increased auditory brainstem response wave interpeak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:7602333
1318928	Large1	LARGE xylosyl- and glucuronyltransferase 1	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:7602333
1318929	Dbx1	developing brain homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16041369
1318929	Dbx1	developing brain homeobox 1	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1318929	Dbx1	developing brain homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151217	MGI			PMID:25864637
1318929	Dbx1	developing brain homeobox 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1318929	Dbx1	developing brain homeobox 1	gene	MP:0001752	abnormal hypothalamus secretion		IAGP		N	RGD:5509061	20151217	MGI			PMID:25864637
1318929	Dbx1	developing brain homeobox 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1318929	Dbx1	developing brain homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151217	MGI			PMID:25864637
1318929	Dbx1	developing brain homeobox 1	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239429
1318929	Dbx1	developing brain homeobox 1	gene	MP:0003462	abnormal response to novel odor		IAGP		N	RGD:5509061	20151217	MGI			PMID:25864637
1318929	Dbx1	developing brain homeobox 1	gene	MP:0005267	abnormal olfactory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16041369
1318929	Dbx1	developing brain homeobox 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20151217	MGI			PMID:25864637
1318929	Dbx1	developing brain homeobox 1	gene	MP:0005423	abnormal somatic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15134635
1318929	Dbx1	developing brain homeobox 1	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20151217	MGI			PMID:25864637
1318929	Dbx1	developing brain homeobox 1	gene	MP:0010745	abnormal pre-Botzinger complex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1318929	Dbx1	developing brain homeobox 1	gene	MP:0010746	abnormal pre-Botzinger complex physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1318929	Dbx1	developing brain homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239429
1318929	Dbx1	developing brain homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1318929	Dbx1	developing brain homeobox 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20151217	MGI			PMID:25864637
1318929	Dbx1	developing brain homeobox 1	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20151217	MGI			PMID:25864637
1318929	Dbx1	developing brain homeobox 1	gene	MP:0021102	abnormal ventral interneuron 0 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:11239429
1318929	Dbx1	developing brain homeobox 1	gene	MP:0021102	abnormal ventral interneuron 0 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15134635
1318929	Dbx1	developing brain homeobox 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25864637
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0003666	impaired sperm capacitation		IAGP		N	RGD:5509061	20190912	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0009242	thin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517695
1318932	Slc26a8	solute carrier family 26, member 8	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:17517695
1318935	Alg5	ALG5 dolichyl-phosphate beta-glucosyltransferase	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1318935	Alg5	ALG5 dolichyl-phosphate beta-glucosyltransferase	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1318935	Alg5	ALG5 dolichyl-phosphate beta-glucosyltransferase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1318935	Alg5	ALG5 dolichyl-phosphate beta-glucosyltransferase	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001317	abnormal pupil morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0002003	miotic pupil		IAGP		N	RGD:5509061	20230713	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0002638	abnormal pupillary reflex		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0006219	optic nerve degeneration		IAGP		N	RGD:5509061	20151224	MGI			PMID:25779931
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0009121	increased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150430	MGI			PMID:24764192
1318942	Rab18	RAB18, member RAS oncogene family	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:24764192
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18288109
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20260402	MGI			
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:9806835
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:9806835
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9806835
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9806835
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:9806835
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:9806835
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18288109
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0003242	loss of basal ganglia neurons		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18288109
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:18288109
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18288109
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:8325640
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18288109
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18288109
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18288109
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509788
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12009762
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:9806835
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0011634	abnormal mitochondrial inner membrane morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318944	Htra2	HtrA serine peptidase 2	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25531304
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0002965	increased circulating serum albumin level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0005337	abnormal retroperitoneal fat pad morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20161229	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240718	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22961760
1318949	Hint2	histidine triad nucleotide binding protein 2	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:22961760
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000138	absent vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000151	absent ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000592	short tail		IEA		N	RGD:5509061	20230928	MGI			
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0000963	fused dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20230928	MGI			
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22659386
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0002632	vestigial tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0003051	curly tail		IEA		N	RGD:5509061	20230928	MGI			
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0003358	abnormal hypaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0004248	abnormal epaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0004653	absent caudal vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0005222	abnormal somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0005421	loose skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0008832	hemivertebra		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925591
1318951	Meox1	mesenchyme homeobox 1	gene	MP:0030286	occipital bone hypoplasia		IAGP		N	RGD:5509061	20171102	MGI			PMID:12925591
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622884
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622884
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622884
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622884
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342461
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622884
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622884
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622884
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622884
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0031152	subcutaneous hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:19633199
1318954	Zfp36l2	zinc finger protein 36, C3H type-like 2	gene	MP:0031154	intestinal hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:19633199
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20141003	MGI			
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318956	Sema5b	sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1318959	Csrnp2	cysteine-serine-rich nuclear protein 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17726538
1318959	Csrnp2	cysteine-serine-rich nuclear protein 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17726538
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20260402	MGI			
1318961	Jkamp	JNK1/MAPK8-associated membrane protein	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1318963	Abraxas2	BRISC complex subunit	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1318963	Abraxas2	BRISC complex subunit	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1318963	Abraxas2	BRISC complex subunit	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20251120	MGI			PMID:33107021
1318963	Abraxas2	BRISC complex subunit	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1318963	Abraxas2	BRISC complex subunit	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1318963	Abraxas2	BRISC complex subunit	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1318963	Abraxas2	BRISC complex subunit	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1318963	Abraxas2	BRISC complex subunit	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1318963	Abraxas2	BRISC complex subunit	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0013374	increased sebaceous gland tumor incidence		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0014040	increased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20250403	MGI			PMID:28860160
1318963	Abraxas2	BRISC complex subunit	gene	MP:0014788	decreased protein level		IAGP		N	RGD:5509061	20251120	MGI			PMID:33107021
1318963	Abraxas2	BRISC complex subunit	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:28860160
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0000467	abnormal esophagus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0003158	dysphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0003159	abnormal esophageal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0003160	abnormal esophagus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0004548	dilated esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318966	Col19a1	collagen, type XIX, alpha 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302855
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318971	Faap20	Fanconi anemia core complex associated protein 20	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1318973	Tax1bp3	Tax1 (human T cell leukemia virus type I) binding protein 3	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1318973	Tax1bp3	Tax1 (human T cell leukemia virus type I) binding protein 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1318973	Tax1bp3	Tax1 (human T cell leukemia virus type I) binding protein 3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1318973	Tax1bp3	Tax1 (human T cell leukemia virus type I) binding protein 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318975	Brd3	bromodomain containing 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1318975	Brd3	bromodomain containing 3	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20220811	MGI			
1318975	Brd3	bromodomain containing 3	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220811	MGI			
1318975	Brd3	bromodomain containing 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1318977	Fkbp6	FK506 binding protein 6	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764197
1318977	Fkbp6	FK506 binding protein 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764197
1318977	Fkbp6	FK506 binding protein 6	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764197
1318977	Fkbp6	FK506 binding protein 6	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1318977	Fkbp6	FK506 binding protein 6	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764197
1318977	Fkbp6	FK506 binding protein 6	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764197
1318979	Nprl2	NPR2 like, GATOR1 complex subunit	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20160929	MGI			PMID:26166573
1318979	Nprl2	NPR2 like, GATOR1 complex subunit	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20160929	MGI			PMID:26166573
1318979	Nprl2	NPR2 like, GATOR1 complex subunit	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20160929	MGI			PMID:26166573
1318979	Nprl2	NPR2 like, GATOR1 complex subunit	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20160929	MGI			PMID:26166573
1318979	Nprl2	NPR2 like, GATOR1 complex subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160929	MGI			PMID:26166573
1318979	Nprl2	NPR2 like, GATOR1 complex subunit	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:26166573
1318979	Nprl2	NPR2 like, GATOR1 complex subunit	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20160929	MGI			PMID:26166573
1318979	Nprl2	NPR2 like, GATOR1 complex subunit	gene	MP:0014399	decreased hematopoietic precursor cell number		IAGP		N	RGD:5509061	20240321	MGI			PMID:26166573
1318979	Nprl2	NPR2 like, GATOR1 complex subunit	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:26166573
1318982	Fam168a	family with sequence similarity 168, member A	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1318982	Fam168a	family with sequence similarity 168, member A	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1318982	Fam168a	family with sequence similarity 168, member A	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201022	MGI			
1318982	Fam168a	family with sequence similarity 168, member A	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20210722	MGI			PMID:30843071
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20210722	MGI			PMID:30843071
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0014252	abnormal paired-pulse ratio		IAGP		N	RGD:5509061	20230706	MGI			PMID:30401835
1318987	Ythdf1	YTH N6-methyladenosine RNA binding protein 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20210722	MGI			PMID:30401835
1318990	Anxa10	annexin A10	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20170518	MGI			PMID:27881083
1318992	Gpatch1	G patch domain containing 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318992	Gpatch1	G patch domain containing 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318992	Gpatch1	G patch domain containing 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1318992	Gpatch1	G patch domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1318994	Anapc10	anaphase promoting complex subunit 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1318994	Anapc10	anaphase promoting complex subunit 10	gene	MP:0012000	abnormal limb position		IEA		N	RGD:5509061	20240523	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210520	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858856
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0000467	abnormal esophagus morphology		IEA		N	RGD:5509061	20190502	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20190502	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20190502	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0000705	athymia		IEA		N	RGD:5509061	20190502	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20190502	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858856
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858856
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20190502	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858856
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0002282	abnormal trachea morphology		IEA		N	RGD:5509061	20190502	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858856
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858856
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858856
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0008024	absent lymph nodes		IEA		N	RGD:5509061	20190502	MGI			
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858856
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858856
1318996	Mmp15	matrix metallopeptidase 15	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1318998	Tnpo3	transportin 3	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141003	MGI			
1319002	Tmod4	tropomodulin 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26586224
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043865
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043865
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043865
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043865
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004524	short cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660251
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004534	decreased inner hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660251
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662770
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662770
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660251
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043865
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043865
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043865
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043865
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662770
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660251
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20240405	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0020811	abnormal photoreceptor outer segment size		IAGP		N	RGD:5509061	20200206	MGI			PMID:30082328
1319004	Fscn2	fascin actin-bundling protein 2	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:16043865
1319006	Gjd3	gap junction protein, delta 3	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571663
1319006	Gjd3	gap junction protein, delta 3	gene	MP:0006141	abnormal atrioventricular node conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571663
1319006	Gjd3	gap junction protein, delta 3	gene	MP:0006142	abnormal sinoatrial node conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982984
1319006	Gjd3	gap junction protein, delta 3	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982984
1319006	Gjd3	gap junction protein, delta 3	gene	MP:0010511	shortened PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982984
1319006	Gjd3	gap junction protein, delta 3	gene	MP:0011953	prolonged PQ interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982984
1319006	Gjd3	gap junction protein, delta 3	gene	MP:0011954	shortened PQ interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571663
1319010	Bnip2	BCL2/adenovirus E1B interacting protein 2	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20201231	MGI			
1319010	Bnip2	BCL2/adenovirus E1B interacting protein 2	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20160421	MGI			
1319010	Bnip2	BCL2/adenovirus E1B interacting protein 2	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20160421	MGI			
1319010	Bnip2	BCL2/adenovirus E1B interacting protein 2	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1319010	Bnip2	BCL2/adenovirus E1B interacting protein 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1319010	Bnip2	BCL2/adenovirus E1B interacting protein 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1319010	Bnip2	BCL2/adenovirus E1B interacting protein 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20181227	MGI			
1319010	Bnip2	BCL2/adenovirus E1B interacting protein 2	gene	MP:0010096	abnormal incisor color		IEA		N	RGD:5509061	20181227	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000151	absent ribs		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201231	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000520	absent kidney		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000819	abnormal olfactory bulb morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0000963	fused dorsal root ganglion		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0001014	absent superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319014	H13	histocompatibility 13	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0002177	abnormal outer ear morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0002766	situs inversus		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319014	H13	histocompatibility 13	gene	MP:0002858	abnormal posterior semicircular canal morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0002951	small thyroid gland		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0003178	left pulmonary isomerism		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0003632	abnormal nervous system morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0004110	transposition of great arteries		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319014	H13	histocompatibility 13	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0004607	abnormal cervical atlas morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0004665	abnormal stapedial artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0004666	absent stapedial artery		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0004686	decreased length of long bones		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319014	H13	histocompatibility 13	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319014	H13	histocompatibility 13	gene	MP:0006425	absent Mullerian ducts		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0008023	abnormal styloid process morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0008128	abnormal brain internal capsule morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319014	H13	histocompatibility 13	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0009770	abnormal optic chiasm morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0009820	abnormal liver vasculature morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1319014	H13	histocompatibility 13	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0010439	abnormal hepatic vein morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319014	H13	histocompatibility 13	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013824	abnormal hypoglossal canal morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013826	absent hypoglossal canal		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013855	absent celiac artery		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013858	abnormal azygos vein topology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013861	abnormal pancreas topology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013864	enlarged paraumbilical vein		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013871	abnormal stapedial artery topology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013915	abnormal brachial plexus formation		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013936	abnormal thymus topology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013966	abnormal infrahyoid muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013977	symmetric azygos veins		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013985	abnormal umbilical vein topology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013992	persistent dorsal ophthalmic artery		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0013996	abnormal vertebral artery origin		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0014006	absent posterior communicating artery		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0014018	embryo tumor		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0014023	abnormal intestine placement		IEA		N	RGD:5509061	20170504	MGI			
1319014	H13	histocompatibility 13	gene	MP:0020493	absent inferior vena cava		IEA		N	RGD:5509061	20180628	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20201022	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20230601	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20210520	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20201022	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210826	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20201022	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20201022	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20201022	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20241121	MGI			
1319016	Rgl1	ral guanine nucleotide dissociation stimulator,-like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319018	Rrh	retinal pigment epithelium derived rhodopsin homolog	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:29109151
1319020	Ptdss1	phosphatidylserine synthase 1	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20170105	MGI			
1319020	Ptdss1	phosphatidylserine synthase 1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18343815
1319020	Ptdss1	phosphatidylserine synthase 1	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20160421	MGI			
1319020	Ptdss1	phosphatidylserine synthase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18343815
1319020	Ptdss1	phosphatidylserine synthase 1	gene	MP:0012361	decreased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1319022	Ap3b2	adaptor-related protein complex 3, beta 2 subunit	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537701
1319022	Ap3b2	adaptor-related protein complex 3, beta 2 subunit	gene	MP:0003492	abnormal involuntary movement		IEA		N	RGD:5509061	20141003	MGI			
1319022	Ap3b2	adaptor-related protein complex 3, beta 2 subunit	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537701
1319022	Ap3b2	adaptor-related protein complex 3, beta 2 subunit	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20160428	MGI			PMID:25917818
1319022	Ap3b2	adaptor-related protein complex 3, beta 2 subunit	gene	MP:0009617	decreased brain zinc level		IAGP		N	RGD:5509061	20251204	MGI			PMID:15537701
1319022	Ap3b2	adaptor-related protein complex 3, beta 2 subunit	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20141003	MGI			
1319027	Mcoln1	mucolipin 1	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21111738
1319027	Mcoln1	mucolipin 1	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21111738
1319027	Mcoln1	mucolipin 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21111738
1319027	Mcoln1	mucolipin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063126
1319027	Mcoln1	mucolipin 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:21111738
1319027	Mcoln1	mucolipin 1	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21111738
1319027	Mcoln1	mucolipin 1	gene	MP:0004731	increased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0004731	increased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21111738
1319027	Mcoln1	mucolipin 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:21111738
1319027	Mcoln1	mucolipin 1	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319027	Mcoln1	mucolipin 1	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17924347
1319029	Cobll1	Cobl-like 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230601	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20230601	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0003918	decreased kidney weight		IEA		N	RGD:5509061	20240523	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1319029	Cobll1	Cobl-like 1	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20230601	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226267
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20160811	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226267
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16221973
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20160811	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226267
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9582278
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11526516
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12901790
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226267
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11526516
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12901790
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226267
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20221215	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20221215	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0008402	increased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9582278
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226267
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226267
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226267
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226267
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9582278
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319032	Mtf1	metal response element binding transcription factor 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1319033	Vstm2a	V-set and transmembrane domain containing 2A	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1319033	Vstm2a	V-set and transmembrane domain containing 2A	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220519	MGI			
1319033	Vstm2a	V-set and transmembrane domain containing 2A	gene	MP:0002759	abnormal caudal vertebrae morphology		IEA		N	RGD:5509061	20220811	MGI			
1319033	Vstm2a	V-set and transmembrane domain containing 2A	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20220519	MGI			
1319033	Vstm2a	V-set and transmembrane domain containing 2A	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20220519	MGI			
1319033	Vstm2a	V-set and transmembrane domain containing 2A	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20220519	MGI			
1319033	Vstm2a	V-set and transmembrane domain containing 2A	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20220519	MGI			
1319038	Wapl	WAPL cohesin release factor	gene	MP:0001697	abnormal embryo size		IAGP		N	RGD:5509061	20230629	MGI			PMID:36449618
1319038	Wapl	WAPL cohesin release factor	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23975099
1319038	Wapl	WAPL cohesin release factor	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23975099
1319038	Wapl	WAPL cohesin release factor	gene	MP:0006204	embryonic lethality before implantation		IAGP		N	RGD:5509061	20230629	MGI			PMID:36449618
1319038	Wapl	WAPL cohesin release factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23975099
1319038	Wapl	WAPL cohesin release factor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20230629	MGI			PMID:36449618
1319038	Wapl	WAPL cohesin release factor	gene	MP:0011705	absent fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23975099
1319040	Pdcd7	programmed cell death 7	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220519	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20220519	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20220811	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20220811	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20241121	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210520	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0001714	absent trophoblast giant cells		IEA		N	RGD:5509061	20240926	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240926	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20231207	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20241121	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0004964	absent inner cell mass		IEA		N	RGD:5509061	20240926	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20221215	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20220519	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20231207	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220811	MGI			
1319040	Pdcd7	programmed cell death 7	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1319042	Plpbp	pyridoxal phosphate binding protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1319044	Lmcd1	LIM and cysteine-rich domains 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1319044	Lmcd1	LIM and cysteine-rich domains 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1319044	Lmcd1	LIM and cysteine-rich domains 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1319044	Lmcd1	LIM and cysteine-rich domains 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319048	Efs	embryonal Fyn-associated substrate	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314525
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0000149	abnormal scapula morphology		IEA		N	RGD:5509061	20141003	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20150430	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0000552	abnormal radius morphology		IEA		N	RGD:5509061	20150430	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20141003	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20160114	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20201231	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0005108	abnormal ulna morphology		IEA		N	RGD:5509061	20150430	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20201231	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20170105	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1319051	Tram2	translocating chain-associating membrane protein 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1319053	Ddost	dolichyl-di-phosphooligosaccharide-protein glycotransferase	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20160811	MGI			
1319053	Ddost	dolichyl-di-phosphooligosaccharide-protein glycotransferase	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1319053	Ddost	dolichyl-di-phosphooligosaccharide-protein glycotransferase	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1319053	Ddost	dolichyl-di-phosphooligosaccharide-protein glycotransferase	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220519	MGI			
1319053	Ddost	dolichyl-di-phosphooligosaccharide-protein glycotransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1319053	Ddost	dolichyl-di-phosphooligosaccharide-protein glycotransferase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1319053	Ddost	dolichyl-di-phosphooligosaccharide-protein glycotransferase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1319055	Icam4	intercellular adhesion molecule 4	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16690966
1319057	Nagpa	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	gene	MP:0003174	increased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710420
1319060	Melk	maternal embryonic leucine zipper kinase	gene	MP:0005518	abnormal pancreas regeneration		IAGP		N	RGD:5509061	20160317	MGI			PMID:25194022
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0001128	ovary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20231207	MGI			
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0001934	increased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20170105	MGI			
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20160114	MGI			
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0002681	increased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0002808	abnormal barbering behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0003378	early sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0004909	increased seminal vesicle weight		IAGP		N	RGD:5509061	20141204	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20231207	MGI			
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0004928	increased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0014272	increased ovary secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:18431515
1319068	Chst8	carbohydrate sulfotransferase 8	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20200402	MGI			
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20200402	MGI			
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20200402	MGI			
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0002293	long gestation period		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20180111	MGI			PMID:28636595
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:28636595
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0012128	abnormal blastocyst formation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0012129	failure of blastocyst formation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1319071	Nlrp9b	NLR family, pyrin domain containing 9B	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:28636595
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768756
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000321	increased bone marrow cell number		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000346	broad head		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884426
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000618	small salivary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:7541529
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773809
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000687	small lymphoid organs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000687	small lymphoid organs		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805749
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768756
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000726	absent lymphocyte		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20190411	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23747725
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805749
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662890
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001790	abnormal immune system physiology		IEA		N	RGD:5509061	20120119	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768756
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768756
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001841	decreased level of surface class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001841	decreased level of surface class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001860	liver inflammation		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001862	interstitial pneumonia		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7957574
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878379
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805749
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11280730
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002009	preneoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7589844
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7541529
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8339285
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584189
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584189
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699352
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8094405
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773809
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8320959
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8094405
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470055
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725754
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8094405
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002459	abnormal B cell physiology		IEA		N	RGD:5509061	20141003	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002473	impaired complement classical pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002494	increased IgM level		IEA		N	RGD:5509061	20180222	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002619	abnormal lymphocyte morphology		IEA		N	RGD:5509061	20141003	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699352
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23747725
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7541529
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002816	colitis		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002879	increased cellular sensitivity to X-ray irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699352
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23747725
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7541529
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7541529
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20230824	MGI			PMID:12897131
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7541529
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768756
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750251
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004503	decreased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725754
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120869
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12525697
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12525697
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20160218	MGI			PMID:12361980
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19450527
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0004978	decreased B-1 B cell number		IEA		N	RGD:5509061	20180927	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8094405
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20180222	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20190530	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005036	diarrhea		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768756
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23747725
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699352
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7541529
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308121
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20201022	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809058
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:11777954
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308121
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591949
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:18785974
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0005673	decreased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591949
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20180927	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662890
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IEA		N	RGD:5509061	20190411	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20190411	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008081	abnormal single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8094405
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008097	increased plasma cell number		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008102	lymph node hyperplasia		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20180222	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20180215	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008195	abnormal professional antigen presenting cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662890
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008402	increased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008466	enlarged mesenteric lymph nodes		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008524	increased plasmacytoid dendritic cell number		IEA		N	RGD:5509061	20180215	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768756
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008755	abnormal immunoglobulin V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008756	abnormal T cell receptor alpha chain V-J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768756
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008759	abnormal T cell receptor delta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008759	abnormal T cell receptor delta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008761	abnormal immunoglobulin light chain V-J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008800	increased small intestinal crypt cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008838	decreased transforming growth factor beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699352
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009332	abnormal splenocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308121
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20210722	MGI			PMID:31795137
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009481	cecum inflammation		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677503
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9768755
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0009856	failure of ejaculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010250	absent thymus cortex		IAGP		N	RGD:5509061	20160324	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010373	myeloid hyperplasia		IEA		N	RGD:5509061	20111116	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9103418
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9834083
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180927	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180222	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180927	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482716
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17668421
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0013741	absent thymus corticomedullary boundary		IAGP		N	RGD:5509061	20150430	MGI			PMID:9990036
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0014127	increased thymoma incidence		IAGP		N	RGD:5509061	20160317	MGI			PMID:9584189
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0014130	thymus cyst		IAGP		N	RGD:5509061	20160324	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0014130	thymus cyst		IAGP		N	RGD:5509061	20160324	MGI			PMID:6823332
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0014130	thymus cyst		IAGP		N	RGD:5509061	20160324	MGI			PMID:7995938
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0014130	thymus cyst		IAGP		N	RGD:5509061	20160324	MGI			PMID:8806787
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:15879151
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20151015	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0020155	enhanced humoral immune response		IEA		N	RGD:5509061	20180222	MGI			
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20230824	MGI			PMID:12897131
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0030983	failure of copulatory plug deposition		IAGP		N	RGD:5509061	20191017	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0031628	abnormal intromission		IAGP		N	RGD:5509061	20240718	MGI			PMID:17478551
1319073	Prkdc	protein kinase, DNA activated, catalytic polypeptide	gene	MP:0031650	decreased mounting behavior		IAGP		N	RGD:5509061	20240905	MGI			PMID:17478551
1319082	Gsdmc	gasdermin C	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20230601	MGI			
1319082	Gsdmc	gasdermin C	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1319082	Gsdmc	gasdermin C	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1319084	Edc4	enhancer of mRNA decapping 4	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1319084	Edc4	enhancer of mRNA decapping 4	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1319084	Edc4	enhancer of mRNA decapping 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319085	Scyl3	SCY1-like 3 (S. cerevisiae)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:29437892
1319088	Ngp	neutrophilic granule protein	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201231	MGI			
1319088	Ngp	neutrophilic granule protein	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20201022	MGI			
1319091	S100a5	S100 calcium binding protein A5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141218	MGI			PMID:25411495
1319091	S100a5	S100 calcium binding protein A5	gene	MP:0011677	abnormal olfactory sensory neuron physiology		IAGP		N	RGD:5509061	20141218	MGI			PMID:25411495
1319093	Nts	neurotensin	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0005457	abnormal percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11427716
1319093	Nts	neurotensin	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:21907138
1319093	Nts	neurotensin	gene	MP:0014441	decreased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:21907138
1319095	Abca6	ATP-binding cassette, sub-family A member 6	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1319095	Abca6	ATP-binding cassette, sub-family A member 6	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20201022	MGI			
1319095	Abca6	ATP-binding cassette, sub-family A member 6	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160421	MGI			
1319095	Abca6	ATP-binding cassette, sub-family A member 6	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20221215	MGI			
1319097	Cldn9	claudin 9	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696885
1319097	Cldn9	claudin 9	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20230119	MGI			
1319097	Cldn9	claudin 9	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696885
1319097	Cldn9	claudin 9	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20230119	MGI			
1319097	Cldn9	claudin 9	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696885
1319097	Cldn9	claudin 9	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696885
1319097	Cldn9	claudin 9	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696885
1319097	Cldn9	claudin 9	gene	MP:0004888	abnormal perilymph physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696885
1319097	Cldn9	claudin 9	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696885
1319097	Cldn9	claudin 9	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696885
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652367
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652367
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0002898	absent cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18543318
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652367
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652367
1319099	Sox6	SRY (sex determining region Y)-box 6	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702786
1319101	Cldn23	claudin 23	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20240523	MGI			
1319101	Cldn23	claudin 23	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1319104	Usp25	ubiquitin specific peptidase 25	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042150
1319104	Usp25	ubiquitin specific peptidase 25	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042150
1319104	Usp25	ubiquitin specific peptidase 25	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042150
1319104	Usp25	ubiquitin specific peptidase 25	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042150
1319104	Usp25	ubiquitin specific peptidase 25	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23042150
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20181227	MGI			
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20181227	MGI			
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20181227	MGI			
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20181227	MGI			
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20181227	MGI			
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0002883	chromatolysis		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20160915	MGI			PMID:24480485
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20160915	MGI			PMID:24480485
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20181227	MGI			
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20160915	MGI			PMID:24480485
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20160915	MGI			PMID:24480485
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20151112	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20160915	MGI			PMID:24480485
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20160915	MGI			PMID:24480485
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0014320	abnormal autopod rotation		IAGP		N	RGD:5509061	20240404	MGI			PMID:25860513
1319107	Gdap1	ganglioside-induced differentiation-associated-protein 1	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20190711	MGI			PMID:24480485
1319112	Ppfia1	protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1319112	Ppfia1	protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1319112	Ppfia1	protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1319112	Ppfia1	protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319117	Rnaseh1	ribonuclease H1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12667461
1319117	Rnaseh1	ribonuclease H1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12667461
1319117	Rnaseh1	ribonuclease H1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12667461
1319117	Rnaseh1	ribonuclease H1	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12667461
1319117	Rnaseh1	ribonuclease H1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12667461
1319117	Rnaseh1	ribonuclease H1	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12667461
1319117	Rnaseh1	ribonuclease H1	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12667461
1319117	Rnaseh1	ribonuclease H1	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20141003	MGI			PMID:12667461
1319117	Rnaseh1	ribonuclease H1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:12667461
1319119	Son	Son DNA binding protein	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1319119	Son	Son DNA binding protein	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0008184	abnormal naive B cell morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0008188	abnormal transitional stage B cell morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0013660	abnormal bone marrow hematopoietic cell morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0013704	increased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:38290089
1319119	Son	Son DNA binding protein	gene	MP:0021182	decreased femoral compact bone area		IAGP		N	RGD:5509061	20240530	MGI			PMID:38290089
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220106	MGI			PMID:34445597
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220106	MGI			PMID:34445597
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20220106	MGI			PMID:34445597
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220106	MGI			PMID:34445597
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220106	MGI			PMID:34445597
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20220106	MGI			PMID:34445597
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220106	MGI			PMID:34445597
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319120	Zdhhc19	zinc finger, DHHC domain containing 19	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220811	MGI			PMID:34897408
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0000075	absent neurocranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20200514	MGI			
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0004383	absent interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0004443	absent supraoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0004459	small alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20160922	MGI			PMID:24833801
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160922	MGI			PMID:24833801
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20160922	MGI			PMID:24833801
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0012686	everted embryonic neuroepithelium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0012702	increased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0012705	increased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20171005	MGI			PMID:18303018
1319122	Scube1	signal peptide, CUB domain, EGF-like 1	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:24833801
1319126	Eif3b	eukaryotic translation initiation factor 3, subunit B	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20150611	MGI			PMID:12038979
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106934
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962153
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962153
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962153
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962153
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962153
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962153
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962153
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106934
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962153
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106934
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21106934
1319132	Bco2	beta-carotene oxygenase 2	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21106934
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150205	MGI			PMID:24706898
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20150205	MGI			PMID:24706898
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20150205	MGI			PMID:24706898
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20150205	MGI			PMID:24706898
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20150205	MGI			PMID:24706898
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0008831	abnormal insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319134	Mex3c	mex3 RNA binding family member C	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357625
1319143	Tomm34	translocase of outer mitochondrial membrane 34	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12801914
1319152	1700008O03Rik	RIKEN cDNA 1700008O03 gene	gene	MP:0002073	abnormal hair growth		IEA		N	RGD:5509061	20201022	MGI			
1319152	1700008O03Rik	RIKEN cDNA 1700008O03 gene	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20201022	MGI			
1319157	Ptch1	patched 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8830098
1319157	Ptch1	patched 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262482
1319157	Ptch1	patched 1	gene	MP:0000373	belly spot		IEA		N	RGD:5509061	20111116	MGI			
1319157	Ptch1	patched 1	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12648487
1319157	Ptch1	patched 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872247
1319157	Ptch1	patched 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055936
1319157	Ptch1	patched 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1319157	Ptch1	patched 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698544
1319157	Ptch1	patched 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000435	shortened head		IEA		N	RGD:5509061	20111116	MGI			
1319157	Ptch1	patched 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1319157	Ptch1	patched 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849540
1319157	Ptch1	patched 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262482
1319157	Ptch1	patched 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262482
1319157	Ptch1	patched 1	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8830098
1319157	Ptch1	patched 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8830098
1319157	Ptch1	patched 1	gene	MP:0000592	short tail		IEA		N	RGD:5509061	20111116	MGI			
1319157	Ptch1	patched 1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20160804	MGI			PMID:24141783
1319157	Ptch1	patched 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319157	Ptch1	patched 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691548
1319157	Ptch1	patched 1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319157	Ptch1	patched 1	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319157	Ptch1	patched 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691548
1319157	Ptch1	patched 1	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319157	Ptch1	patched 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319157	Ptch1	patched 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698544
1319157	Ptch1	patched 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1319157	Ptch1	patched 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872247
1319157	Ptch1	patched 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321799
1319157	Ptch1	patched 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262482
1319157	Ptch1	patched 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872247
1319157	Ptch1	patched 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319157	Ptch1	patched 1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8830098
1319157	Ptch1	patched 1	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:8830098
1319157	Ptch1	patched 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20171207	MGI			PMID:23404854
1319157	Ptch1	patched 1	gene	MP:0001247	dermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262482
1319157	Ptch1	patched 1	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160804	MGI			PMID:24141783
1319157	Ptch1	patched 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0001300	ocular hypertelorism		IEA		N	RGD:5509061	20111116	MGI			
1319157	Ptch1	patched 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213072
1319157	Ptch1	patched 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668681
1319157	Ptch1	patched 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319157	Ptch1	patched 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698544
1319157	Ptch1	patched 1	gene	MP:0001699	increased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0001699	increased embryo size		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872247
1319157	Ptch1	patched 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20171207	MGI			PMID:23404854
1319157	Ptch1	patched 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20171207	MGI			PMID:23404854
1319157	Ptch1	patched 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20200611	MGI			PMID:30452905
1319157	Ptch1	patched 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12648487
1319157	Ptch1	patched 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20171207	MGI			PMID:23404854
1319157	Ptch1	patched 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1319157	Ptch1	patched 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20111116	MGI			
1319157	Ptch1	patched 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849540
1319157	Ptch1	patched 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321799
1319157	Ptch1	patched 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1319157	Ptch1	patched 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262482
1319157	Ptch1	patched 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200611	MGI			PMID:30452905
1319157	Ptch1	patched 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15475264
1319157	Ptch1	patched 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849540
1319157	Ptch1	patched 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047082
1319157	Ptch1	patched 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1319157	Ptch1	patched 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321799
1319157	Ptch1	patched 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872247
1319157	Ptch1	patched 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1319157	Ptch1	patched 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849540
1319157	Ptch1	patched 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1319157	Ptch1	patched 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691548
1319157	Ptch1	patched 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321799
1319157	Ptch1	patched 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160804	MGI			PMID:24141783
1319157	Ptch1	patched 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1319157	Ptch1	patched 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1319157	Ptch1	patched 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1319157	Ptch1	patched 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22549777
1319157	Ptch1	patched 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872247
1319157	Ptch1	patched 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15269168
1319157	Ptch1	patched 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18272593
1319157	Ptch1	patched 1	gene	MP:0002271	abnormal pulmonary alveolar duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0002286	cryptorchism		IEA		N	RGD:5509061	20111116	MGI			
1319157	Ptch1	patched 1	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20018657
1319157	Ptch1	patched 1	gene	MP:0002716	small male preputial gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:8830098
1319157	Ptch1	patched 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0003190	fused synovial joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321799
1319157	Ptch1	patched 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233865
1319157	Ptch1	patched 1	gene	MP:0003460	decreased fear-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8830098
1319157	Ptch1	patched 1	gene	MP:0003580	increased fibroma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321799
1319157	Ptch1	patched 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1319157	Ptch1	patched 1	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1319157	Ptch1	patched 1	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698544
1319157	Ptch1	patched 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20160804	MGI			PMID:24141783
1319157	Ptch1	patched 1	gene	MP:0003841	abnormal lambdoid suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1319157	Ptch1	patched 1	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12386820
1319157	Ptch1	patched 1	gene	MP:0004175	telangiectasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849540
1319157	Ptch1	patched 1	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1319157	Ptch1	patched 1	gene	MP:0004199	increased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0004199	increased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849540
1319157	Ptch1	patched 1	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321799
1319157	Ptch1	patched 1	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233865
1319157	Ptch1	patched 1	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20171207	MGI			PMID:23404854
1319157	Ptch1	patched 1	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20181220	MGI			PMID:10545995
1319157	Ptch1	patched 1	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0004460	alisphenoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0004478	increased testicular teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849540
1319157	Ptch1	patched 1	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12386820
1319157	Ptch1	patched 1	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20180621	MGI			PMID:21351254
1319157	Ptch1	patched 1	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20181220	MGI			PMID:10545995
1319157	Ptch1	patched 1	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20181220	MGI			PMID:10545995
1319157	Ptch1	patched 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20171207	MGI			PMID:23404854
1319157	Ptch1	patched 1	gene	MP:0004733	abnormal thoracic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8830098
1319157	Ptch1	patched 1	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1319157	Ptch1	patched 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691548
1319157	Ptch1	patched 1	gene	MP:0004971	dermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8830098
1319157	Ptch1	patched 1	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691548
1319157	Ptch1	patched 1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869526
1319157	Ptch1	patched 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668681
1319157	Ptch1	patched 1	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319157	Ptch1	patched 1	gene	MP:0005503	abnormal tendon morphology		IEA		N	RGD:5509061	20111116	MGI			
1319157	Ptch1	patched 1	gene	MP:0005508	abnormal skeleton morphology		IEA		N	RGD:5509061	20111116	MGI			
1319157	Ptch1	patched 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12386820
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260494
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849540
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17047082
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691548
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19185848
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213072
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321799
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343890
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262482
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20180621	MGI			PMID:21351254
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20200611	MGI			PMID:30452905
1319157	Ptch1	patched 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20240404	MGI			PMID:38517960
1319157	Ptch1	patched 1	gene	MP:0006292	abnormal nasal placode morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0006343	enlarged first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0006344	small second pharyngeal arch		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17536012
1319157	Ptch1	patched 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20160804	MGI			PMID:24141783
1319157	Ptch1	patched 1	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1319157	Ptch1	patched 1	gene	MP:0008785	abnormal sternum manubrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0008914	enlarged cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691548
1319157	Ptch1	patched 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20200611	MGI			PMID:30452905
1319157	Ptch1	patched 1	gene	MP:0009882	absent palatal shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260494
1319157	Ptch1	patched 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0010283	decreased classified tumor incidence		IAGP		N	RGD:5509061	20240404	MGI			PMID:38517960
1319157	Ptch1	patched 1	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12648487
1319157	Ptch1	patched 1	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16849540
1319157	Ptch1	patched 1	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0010643	absent fourth pharyngeal arch		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0010939	abnormal mandibular prominence morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372258
1319157	Ptch1	patched 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1319157	Ptch1	patched 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1319157	Ptch1	patched 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262482
1319157	Ptch1	patched 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11668681
1319157	Ptch1	patched 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319157	Ptch1	patched 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061793
1319157	Ptch1	patched 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19321799
1319157	Ptch1	patched 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1319157	Ptch1	patched 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20171214	MGI			PMID:21305688
1319157	Ptch1	patched 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0011712	arrested osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0011934	abnormal branching involved in pancreas development		IAGP		N	RGD:5509061	20141218	MGI			PMID:12917290
1319157	Ptch1	patched 1	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872247
1319157	Ptch1	patched 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0012525	abnormal rhombic lip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691548
1319157	Ptch1	patched 1	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1319157	Ptch1	patched 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1319157	Ptch1	patched 1	gene	MP:0013551	decreased cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20200611	MGI			PMID:30452905
1319157	Ptch1	patched 1	gene	MP:0013945	abnormal elbow joint morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0014100	increased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20240404	MGI			PMID:38517960
1319157	Ptch1	patched 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:19147535
1319157	Ptch1	patched 1	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:16936073
1319157	Ptch1	patched 1	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:12361967
1319157	Ptch1	patched 1	gene	MP:0021217	abnormal palatal shelf bone ossification		IAGP		N	RGD:5509061	20230223	MGI			PMID:21364421
1319157	Ptch1	patched 1	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:20018657
1319157	Ptch1	patched 1	gene	MP:0030220	mandibular cyst		IAGP		N	RGD:5509061	20171019	MGI			PMID:12542834
1319157	Ptch1	patched 1	gene	MP:0030220	mandibular cyst		IAGP		N	RGD:5509061	20171019	MGI			PMID:9585239
1319157	Ptch1	patched 1	gene	MP:0030284	short mandibular coronoid process		IAGP		N	RGD:5509061	20171102	MGI			PMID:23897749
1319157	Ptch1	patched 1	gene	MP:0030285	mandibular coronoid process hypoplasia		IAGP		N	RGD:5509061	20171102	MGI			PMID:23897749
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20181227	MGI			
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20181227	MGI			
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:27875292
1319161	Zdhhc3	zinc finger, DHHC domain containing 3	gene	MP:0020358	abnormal inhibitory synapse morphology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20210128	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20230601	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:17971852
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0020858	cornea epithelium hypoplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:17971852
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0020861	abnormal cornea wound healing		IAGP		N	RGD:5509061	20181101	MGI			PMID:17971852
1319163	Bnc1	basonuclin zinc finger protein 1	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20250605	MGI			PMID:30010909
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9506940
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514218
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514218
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514218
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9506940
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9506940
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9506940
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514218
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514218
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20210128	MGI			
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210128	MGI			
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990068
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0002774	small prostate gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9506940
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17045797
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9506940
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005119	decreased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10202153
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005468	abnormal thyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10202153
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005470	increased thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10202153
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005474	increased triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10202153
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005477	increased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005480	increased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576486
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005630	increased lung weight		IEA		N	RGD:5509061	20241121	MGI			
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20220915	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15312245
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1319168	Ncoa1	nuclear receptor coactivator 1	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:15312245
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0003939	abnormal myotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0004677	truncated ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319170	Dmrt2	doublesex and mab-3 related transcription factor 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16387292
1319172	Snapc4	small nuclear RNA activating complex, polypeptide 4	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20160804	MGI			
1319177	Dpf3	double PHD fingers 3	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1319177	Dpf3	double PHD fingers 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210826	MGI			
1319177	Dpf3	double PHD fingers 3	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1319177	Dpf3	double PHD fingers 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210520	MGI			
1319177	Dpf3	double PHD fingers 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0005227	abnormal vertebral body development		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0005229	abnormal intervertebral disk development		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159818
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159818
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0014561	decreased cortical ventricular zone cell density		IAGP		N	RGD:5509061	20241031	MGI			PMID:24013503
1319179	Prmt5	protein arginine N-methyltransferase 5	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20220519	MGI			PMID:31848143
1319180	Tcf25	transcription factor 25 (basic helix-loop-helix)	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1319180	Tcf25	transcription factor 25 (basic helix-loop-helix)	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1319180	Tcf25	transcription factor 25 (basic helix-loop-helix)	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1319180	Tcf25	transcription factor 25 (basic helix-loop-helix)	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1319180	Tcf25	transcription factor 25 (basic helix-loop-helix)	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20240530	MGI			PMID:32805187
1319180	Tcf25	transcription factor 25 (basic helix-loop-helix)	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20240523	MGI			
1319180	Tcf25	transcription factor 25 (basic helix-loop-helix)	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1319182	Ngef	neuronal guanine nucleotide exchange factor	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20170209	MGI			PMID:15848799
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000199	abnormal circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713561
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20141003	MGI			PMID:21804564
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713561
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713561
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501569
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723219
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21804564
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0003282	gastric ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501569
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501569
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501569
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501569
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501569
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008136	enlarged Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923499
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053834
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21804564
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0009582	abnormal keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713561
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713561
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723219
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0011707	impaired fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412431
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1319184	Cyld	CYLD lysine 63 deubiquitinase	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:21804564
1319186	Tbx4	T-box 4	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152185
1319186	Tbx4	T-box 4	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1319186	Tbx4	T-box 4	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1319186	Tbx4	T-box 4	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21932311
1319186	Tbx4	T-box 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23328398
1319186	Tbx4	T-box 4	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579682
1319186	Tbx4	T-box 4	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579682
1319186	Tbx4	T-box 4	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579682
1319186	Tbx4	T-box 4	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579682
1319186	Tbx4	T-box 4	gene	MP:0003230	abnormal umbilical artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0003891	increased allantois apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0004349	absent femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0004507	abnormal ischium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579682
1319186	Tbx4	T-box 4	gene	MP:0004558	delayed allantois development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0004559	small allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579682
1319186	Tbx4	T-box 4	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579682
1319186	Tbx4	T-box 4	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152185
1319186	Tbx4	T-box 4	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579682
1319186	Tbx4	T-box 4	gene	MP:0009656	delayed chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170105	MGI			
1319186	Tbx4	T-box 4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0012134	absent umbilical cord		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0013169	small hindlimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736212
1319186	Tbx4	T-box 4	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1319186	Tbx4	T-box 4	gene	MP:0014281	hindlimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:17164415
1319186	Tbx4	T-box 4	gene	MP:0030860	patellar dislocation		IAGP		N	RGD:5509061	20181025	MGI			PMID:18579682
1319188	Fam161b	family with sequence similarity 161, member B	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20220519	MGI			
1319188	Fam161b	family with sequence similarity 161, member B	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20220519	MGI			
1319188	Fam161b	family with sequence similarity 161, member B	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1319188	Fam161b	family with sequence similarity 161, member B	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1319188	Fam161b	family with sequence similarity 161, member B	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1319188	Fam161b	family with sequence similarity 161, member B	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220519	MGI			
1319188	Fam161b	family with sequence similarity 161, member B	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1319188	Fam161b	family with sequence similarity 161, member B	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230601	MGI			
1319188	Fam161b	family with sequence similarity 161, member B	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20181227	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0002314	abnormal respiratory mechanics		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0003257	abnormal abdominal wall morphology		IEA		N	RGD:5509061	20181227	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20240523	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0011471	decreased urine creatinine level		IEA		N	RGD:5509061	20260402	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1319190	Irx1	Iroquois homeobox 1	gene	MP:0030080	small lower incisors		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0030089	short lower incisors		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0030453	abnormal odontoblast morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0030471	abnormal ameloblast differentiation		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0030508	abnormal dental epithelium morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0030518	abnormal outer dental epithelium morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319190	Irx1	Iroquois homeobox 1	gene	MP:0030523	abnormal stratum intermedium morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:28746823
1319192	Neurog2	neurogenin 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640277
1319192	Neurog2	neurogenin 2	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448566
1319192	Neurog2	neurogenin 2	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640277
1319192	Neurog2	neurogenin 2	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448566
1319192	Neurog2	neurogenin 2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640277
1319192	Neurog2	neurogenin 2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133851
1319192	Neurog2	neurogenin 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20151112	MGI			PMID:18400164
1319192	Neurog2	neurogenin 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825874
1319192	Neurog2	neurogenin 2	gene	MP:0001034	abnormal parasympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133851
1319192	Neurog2	neurogenin 2	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133851
1319192	Neurog2	neurogenin 2	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539123
1319192	Neurog2	neurogenin 2	gene	MP:0001084	abnormal petrosal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539123
1319192	Neurog2	neurogenin 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539123
1319192	Neurog2	neurogenin 2	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539123
1319192	Neurog2	neurogenin 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539123
1319192	Neurog2	neurogenin 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539123
1319192	Neurog2	neurogenin 2	gene	MP:0002751	abnormal autonomic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133851
1319192	Neurog2	neurogenin 2	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133851
1319192	Neurog2	neurogenin 2	gene	MP:0002983	increased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448566
1319192	Neurog2	neurogenin 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539123
1319192	Neurog2	neurogenin 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448566
1319192	Neurog2	neurogenin 2	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448566
1319192	Neurog2	neurogenin 2	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705040
1319192	Neurog2	neurogenin 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448566
1319192	Neurog2	neurogenin 2	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0008031	decreased Cajal-Retzius cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579678
1319192	Neurog2	neurogenin 2	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640277
1319192	Neurog2	neurogenin 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705040
1319192	Neurog2	neurogenin 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448566
1319192	Neurog2	neurogenin 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539123
1319192	Neurog2	neurogenin 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448566
1319192	Neurog2	neurogenin 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539123
1319192	Neurog2	neurogenin 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640277
1319192	Neurog2	neurogenin 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1319192	Neurog2	neurogenin 2	gene	MP:0021091	abnormal dorsal interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15901662
1319192	Neurog2	neurogenin 2	gene	MP:0021093	abnormal dorsal interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15901662
1319192	Neurog2	neurogenin 2	gene	MP:0021094	abnormal dorsal interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15901662
1319192	Neurog2	neurogenin 2	gene	MP:0021095	abnormal dorsal interneuron 4 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15901662
1319192	Neurog2	neurogenin 2	gene	MP:0021096	abnormal dorsal interneuron 5 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15901662
1319192	Neurog2	neurogenin 2	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:18400164
1319192	Neurog2	neurogenin 2	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:15105417
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9492006
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371356
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22588720
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091879
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091879
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151598
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18441309
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:9834104
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18441309
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18441309
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371356
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11086031
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151598
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001573	abnormal circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960353
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371356
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18441309
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441072
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441072
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441072
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371356
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18441309
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371356
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18441309
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10486156
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147789
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371356
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091879
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091879
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11086031
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091879
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002334	abnormal airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11839568
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002334	abnormal airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091879
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11839568
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960353
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602264
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960353
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11839568
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151598
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719110
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602263
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624821
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9834104
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602263
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602263
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9492006
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960353
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12709397
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200068
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11839568
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371356
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101429
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0004481	abnormal conjunctival epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18441309
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721841
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721841
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602264
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0004881	abnormal lung size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091879
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18441309
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17873878
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213110
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9492006
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602264
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11086031
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602263
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602263
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624821
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602264
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18441309
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101429
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602263
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17611223
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22588720
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727894
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602264
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9834104
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008091	decreased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21460847
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719110
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602264
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624821
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151598
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602263
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9834104
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441072
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9492006
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9834104
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960353
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441072
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721841
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9834104
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624821
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008588	abnormal circulating interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008601	abnormal circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008625	abnormal circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151598
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9834104
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441072
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10486156
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441072
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721841
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624821
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624821
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960353
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719110
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008724	impaired eosinophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960353
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19147789
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22588720
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0010064	increased circulating creatine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12709397
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0010174	decreased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22588720
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0010942	abnormal respiratory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11839568
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0010942	abnormal respiratory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500796
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101429
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:12441072
1319195	Stat6	signal transducer and activator of transcription 6	gene	MP:0030757	abnormal circulating histamine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:12151598
1319199	Adam24	ADAM metallopeptidase domain 24	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19670298
1319199	Adam24	ADAM metallopeptidase domain 24	gene	MP:0031014	polyspermy		IAGP		N	RGD:5509061	20200130	MGI			PMID:19670298
1319202	Adprs	ADP-ribosylserine hydrolase	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20220519	MGI			
1319202	Adprs	ADP-ribosylserine hydrolase	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20220519	MGI			
1319202	Adprs	ADP-ribosylserine hydrolase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220519	MGI			
1319202	Adprs	ADP-ribosylserine hydrolase	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20201001	MGI			PMID:30830864
1319202	Adprs	ADP-ribosylserine hydrolase	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1319202	Adprs	ADP-ribosylserine hydrolase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1319202	Adprs	ADP-ribosylserine hydrolase	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1319202	Adprs	ADP-ribosylserine hydrolase	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20201001	MGI			PMID:30830864
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20231012	MGI			PMID:35343376
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20231012	MGI			PMID:35343376
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20231012	MGI			PMID:35343376
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20231012	MGI			PMID:35343376
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20231012	MGI			PMID:35343376
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20231012	MGI			PMID:35343376
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0013732	mature cataract		IAGP		N	RGD:5509061	20231012	MGI			PMID:35343376
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1319204	Fyco1	FYVE and coiled-coil domain containing 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20231012	MGI			PMID:35343376
1319206	Ctsa	cathepsin A	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0000550	abnormal forelimb morphology		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0000556	abnormal hindlimb morphology		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20240523	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0006083	abnormal blood vessel elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0008418	abnormal cutaneous elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20221215	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210520	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0009456	impaired cued conditioning behavior		IEA		N	RGD:5509061	20230601	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:18391110
1319206	Ctsa	cathepsin A	gene	MP:0012175	flat face		IAGP		N	RGD:5509061	20171109	MGI			PMID:7590240
1319206	Ctsa	cathepsin A	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
1319206	Ctsa	cathepsin A	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564878
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220428	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056615
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056615
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056615
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002673	abnormal sperm number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002785	absent Leydig cells		IAGP		N	RGD:5509061	20150319	MGI			PMID:15056615
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564878
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056615
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0005652	sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056615
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564878
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0011971	increased circulating lactate dehydrogenase level		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20260402	MGI			
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0014684	impaired spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:18342849
1319209	Sox8	SRY (sex determining region Y)-box 8	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:18342849
1319210	Fbxo48	F-box protein 48	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20241121	MGI			
1319210	Fbxo48	F-box protein 48	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1319210	Fbxo48	F-box protein 48	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16597604
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170381
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1319221	Gadd45b	growth arrest and DNA-damage-inducible 45 beta	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:16287712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000022	abnormal ear shape		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20170406	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000447	flattened snout		IAGP		N	RGD:5509061	20170921	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20170406	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20210422	MGI			PMID:33431871
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170406	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210422	MGI			PMID:25346535
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210422	MGI			PMID:33431871
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210422	MGI			PMID:33431871
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20170406	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20240215	MGI			PMID:16972005
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20150122	MGI			PMID:24368734
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20150122	MGI			PMID:24368734
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24368734
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002729	abnormal inner ear canal morphology		IAGP		N	RGD:5509061	20170406	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20210422	MGI			PMID:25346535
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20250508	MGI			
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20150122	MGI			PMID:24368734
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20210422	MGI			PMID:25346535
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20210422	MGI			PMID:25346535
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20200730	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33431871
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20250508	MGI			
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20250508	MGI			
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20210422	MGI			PMID:25346535
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008285	abnormal hippocampus granule cell layer		IAGP		N	RGD:5509061	20170406	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20250508	MGI			
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20210422	MGI			PMID:33431871
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20170406	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150122	MGI			PMID:24368734
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141016	MGI			PMID:24368734
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170406	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011170	abnormal brown fat cell differentiation		IAGP		N	RGD:5509061	20150122	MGI			PMID:24368734
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20240404	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20210422	MGI			PMID:33431871
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20170406	MGI			PMID:25273096
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20210422	MGI			PMID:25346535
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20210422	MGI			PMID:25346535
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0030065	face hypoplasia		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0030069	broad face		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0030259	mandibular condyloid process hypoplasia		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0030320	abnormal temporal bone tympanic part morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:30891914
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0031444	glossoptosis		IAGP		N	RGD:5509061	20221027	MGI			PMID:32541010
1319223	Kmt2d	lysine (K)-specific methyltransferase 2D	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:32541010
1319229	Cd19	CD19 antigen	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
1319229	Cd19	CD19 antigen	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070163
1319229	Cd19	CD19 antigen	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1319229	Cd19	CD19 antigen	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120817
1319229	Cd19	CD19 antigen	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668867
1319229	Cd19	CD19 antigen	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782029
1319229	Cd19	CD19 antigen	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1319229	Cd19	CD19 antigen	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439541
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23619366
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20150219	MGI			PMID:24241423
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1319229	Cd19	CD19 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1319229	Cd19	CD19 antigen	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1319229	Cd19	CD19 antigen	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23619366
1319229	Cd19	CD19 antigen	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148088
1319229	Cd19	CD19 antigen	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1319229	Cd19	CD19 antigen	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1319229	Cd19	CD19 antigen	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
1319229	Cd19	CD19 antigen	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507897
1319229	Cd19	CD19 antigen	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1319229	Cd19	CD19 antigen	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1319229	Cd19	CD19 antigen	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1319229	Cd19	CD19 antigen	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668867
1319229	Cd19	CD19 antigen	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420047
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12707341
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17000121
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270713
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1319229	Cd19	CD19 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20231102	MGI			PMID:35439434
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12707341
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16455962
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270713
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7543183
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1319229	Cd19	CD19 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1319229	Cd19	CD19 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070163
1319229	Cd19	CD19 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1319229	Cd19	CD19 antigen	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439541
1319229	Cd19	CD19 antigen	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20150219	MGI			PMID:24241423
1319229	Cd19	CD19 antigen	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060366
1319229	Cd19	CD19 antigen	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930766
1319229	Cd19	CD19 antigen	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1319229	Cd19	CD19 antigen	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439541
1319229	Cd19	CD19 antigen	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1319229	Cd19	CD19 antigen	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060366
1319229	Cd19	CD19 antigen	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1319229	Cd19	CD19 antigen	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439541
1319229	Cd19	CD19 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930766
1319229	Cd19	CD19 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174151
1319229	Cd19	CD19 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1319229	Cd19	CD19 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1319229	Cd19	CD19 antigen	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420047
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668867
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520246
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20156974
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124917
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7543183
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1319229	Cd19	CD19 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1319229	Cd19	CD19 antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244677
1319229	Cd19	CD19 antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22589392
1319229	Cd19	CD19 antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22666421
1319229	Cd19	CD19 antigen	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:27135738
1319229	Cd19	CD19 antigen	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809737
1319229	Cd19	CD19 antigen	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1319229	Cd19	CD19 antigen	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12753744
1319229	Cd19	CD19 antigen	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1319229	Cd19	CD19 antigen	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178004
1319229	Cd19	CD19 antigen	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23772037
1319229	Cd19	CD19 antigen	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520246
1319229	Cd19	CD19 antigen	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174151
1319229	Cd19	CD19 antigen	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1319229	Cd19	CD19 antigen	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1319229	Cd19	CD19 antigen	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1319229	Cd19	CD19 antigen	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148088
1319229	Cd19	CD19 antigen	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1319229	Cd19	CD19 antigen	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17000121
1319229	Cd19	CD19 antigen	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20150219	MGI			PMID:24241423
1319229	Cd19	CD19 antigen	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070163
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809737
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11896394
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563260
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311600
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782029
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023430
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832734
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270713
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23772037
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7543183
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1319229	Cd19	CD19 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1319229	Cd19	CD19 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420047
1319229	Cd19	CD19 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809737
1319229	Cd19	CD19 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520246
1319229	Cd19	CD19 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319229	Cd19	CD19 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1319229	Cd19	CD19 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1319229	Cd19	CD19 antigen	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148088
1319229	Cd19	CD19 antigen	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7543183
1319229	Cd19	CD19 antigen	gene	MP:0002491	decreased IgD level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7543183
1319229	Cd19	CD19 antigen	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070163
1319229	Cd19	CD19 antigen	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070163
1319229	Cd19	CD19 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17000121
1319229	Cd19	CD19 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1319229	Cd19	CD19 antigen	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1319229	Cd19	CD19 antigen	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
1319229	Cd19	CD19 antigen	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1319229	Cd19	CD19 antigen	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23619366
1319229	Cd19	CD19 antigen	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1319229	Cd19	CD19 antigen	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23619366
1319229	Cd19	CD19 antigen	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23657012
1319229	Cd19	CD19 antigen	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
1319229	Cd19	CD19 antigen	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23619366
1319229	Cd19	CD19 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1319229	Cd19	CD19 antigen	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1319229	Cd19	CD19 antigen	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0004795	decreased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0004798	decreased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0004798	decreased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507897
1319229	Cd19	CD19 antigen	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832734
1319229	Cd19	CD19 antigen	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23772037
1319229	Cd19	CD19 antigen	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809737
1319229	Cd19	CD19 antigen	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22547703
1319229	Cd19	CD19 antigen	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420047
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17000121
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178811
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270713
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22547703
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1319229	Cd19	CD19 antigen	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
1319229	Cd19	CD19 antigen	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1319229	Cd19	CD19 antigen	gene	MP:0004940	abnormal B-1 B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070163
1319229	Cd19	CD19 antigen	gene	MP:0004944	abnormal B cell negative selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896393
1319229	Cd19	CD19 antigen	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1319229	Cd19	CD19 antigen	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1319229	Cd19	CD19 antigen	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1319229	Cd19	CD19 antigen	gene	MP:0004976	abnormal B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070163
1319229	Cd19	CD19 antigen	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563260
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235208
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563260
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12707341
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520246
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148088
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431510
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7543183
1319229	Cd19	CD19 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1319229	Cd19	CD19 antigen	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1319229	Cd19	CD19 antigen	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563260
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782029
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060366
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178004
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174151
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23619366
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20150219	MGI			PMID:24241423
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809737
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12707341
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668867
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314171
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148088
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940357
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896393
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1319229	Cd19	CD19 antigen	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163229
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809737
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12707341
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148088
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270713
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22547703
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20161013	MGI			PMID:23343763
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20171026	MGI			PMID:22802351
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1319229	Cd19	CD19 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1319229	Cd19	CD19 antigen	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439541
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235208
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563260
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896393
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1319229	Cd19	CD19 antigen	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120817
1319229	Cd19	CD19 antigen	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439541
1319229	Cd19	CD19 antigen	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0005432	abnormal pro-B cell morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0005433	absent early pro-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668867
1319229	Cd19	CD19 antigen	gene	MP:0005434	absent late pro-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668867
1319229	Cd19	CD19 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1319229	Cd19	CD19 antigen	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148088
1319229	Cd19	CD19 antigen	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
1319229	Cd19	CD19 antigen	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20150219	MGI			PMID:24241423
1319229	Cd19	CD19 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507897
1319229	Cd19	CD19 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20150219	MGI			PMID:24241423
1319229	Cd19	CD19 antigen	gene	MP:0008093	abnormal memory B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0008093	abnormal memory B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1319229	Cd19	CD19 antigen	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
1319229	Cd19	CD19 antigen	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1319229	Cd19	CD19 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189736
1319229	Cd19	CD19 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520246
1319229	Cd19	CD19 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1319229	Cd19	CD19 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1319229	Cd19	CD19 antigen	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270713
1319229	Cd19	CD19 antigen	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1319229	Cd19	CD19 antigen	gene	MP:0008100	absent plasma cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070163
1319229	Cd19	CD19 antigen	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1319229	Cd19	CD19 antigen	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1319229	Cd19	CD19 antigen	gene	MP:0008136	enlarged Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070163
1319229	Cd19	CD19 antigen	gene	MP:0008164	abnormal B-1a B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0008166	abnormal B-2 B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060366
1319229	Cd19	CD19 antigen	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008170	decreased B-1b cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1319229	Cd19	CD19 antigen	gene	MP:0008172	abnormal follicular B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008172	abnormal follicular B cell morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20156974
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178004
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809737
1319229	Cd19	CD19 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235208
1319229	Cd19	CD19 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1319229	Cd19	CD19 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1319229	Cd19	CD19 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870947
1319229	Cd19	CD19 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178004
1319229	Cd19	CD19 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23619366
1319229	Cd19	CD19 antigen	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1319229	Cd19	CD19 antigen	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1319229	Cd19	CD19 antigen	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270713
1319229	Cd19	CD19 antigen	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1319229	Cd19	CD19 antigen	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563260
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178811
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178004
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235208
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12707341
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12753744
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16148088
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023430
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17600736
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870947
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431510
1319229	Cd19	CD19 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12753744
1319229	Cd19	CD19 antigen	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1319229	Cd19	CD19 antigen	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:20156974
1319229	Cd19	CD19 antigen	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0008188	abnormal transitional stage B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178004
1319229	Cd19	CD19 antigen	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12753744
1319229	Cd19	CD19 antigen	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1319229	Cd19	CD19 antigen	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1319229	Cd19	CD19 antigen	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715907
1319229	Cd19	CD19 antigen	gene	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1319229	Cd19	CD19 antigen	gene	MP:0008206	increased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1319229	Cd19	CD19 antigen	gene	MP:0008206	increased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178004
1319229	Cd19	CD19 antigen	gene	MP:0008206	increased B-2 B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520246
1319229	Cd19	CD19 antigen	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1319229	Cd19	CD19 antigen	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420047
1319229	Cd19	CD19 antigen	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809737
1319229	Cd19	CD19 antigen	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1319229	Cd19	CD19 antigen	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1319229	Cd19	CD19 antigen	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:31921164
1319229	Cd19	CD19 antigen	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1319229	Cd19	CD19 antigen	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420047
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235208
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520246
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870947
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1319229	Cd19	CD19 antigen	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1319229	Cd19	CD19 antigen	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
1319229	Cd19	CD19 antigen	gene	MP:0008213	absent immature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1319229	Cd19	CD19 antigen	gene	MP:0008213	absent immature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
1319229	Cd19	CD19 antigen	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420047
1319229	Cd19	CD19 antigen	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235208
1319229	Cd19	CD19 antigen	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1319229	Cd19	CD19 antigen	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12707341
1319229	Cd19	CD19 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270713
1319229	Cd19	CD19 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0008233	abnormal pro-B cell differentiation		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0008240	abnormal spleen marginal zone macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
1319229	Cd19	CD19 antigen	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1319229	Cd19	CD19 antigen	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1319229	Cd19	CD19 antigen	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870947
1319229	Cd19	CD19 antigen	gene	MP:0008473	abnormal spleen follicular dendritic cell network		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1319229	Cd19	CD19 antigen	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563260
1319229	Cd19	CD19 antigen	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:7543183
1319229	Cd19	CD19 antigen	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20060366
1319229	Cd19	CD19 antigen	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1319229	Cd19	CD19 antigen	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563260
1319229	Cd19	CD19 antigen	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1319229	Cd19	CD19 antigen	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1319229	Cd19	CD19 antigen	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420047
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16455962
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7543183
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160721	MGI			PMID:26366712
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20231102	MGI			PMID:35439434
1319229	Cd19	CD19 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1319229	Cd19	CD19 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16455962
1319229	Cd19	CD19 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509585
1319229	Cd19	CD19 antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420047
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16455962
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19270713
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7542548
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1319229	Cd19	CD19 antigen	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1319229	Cd19	CD19 antigen	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166635
1319229	Cd19	CD19 antigen	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120817
1319229	Cd19	CD19 antigen	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507897
1319229	Cd19	CD19 antigen	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620304
1319229	Cd19	CD19 antigen	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1319229	Cd19	CD19 antigen	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507897
1319229	Cd19	CD19 antigen	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0008728	increased memory B cell number		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1319229	Cd19	CD19 antigen	gene	MP:0008746	abnormal peripheral B cell anergy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19896393
1319229	Cd19	CD19 antigen	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563260
1319229	Cd19	CD19 antigen	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12707341
1319229	Cd19	CD19 antigen	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668867
1319229	Cd19	CD19 antigen	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1319229	Cd19	CD19 antigen	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319229	Cd19	CD19 antigen	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1319229	Cd19	CD19 antigen	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782029
1319229	Cd19	CD19 antigen	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20705491
1319229	Cd19	CD19 antigen	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1319229	Cd19	CD19 antigen	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
1319229	Cd19	CD19 antigen	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782029
1319229	Cd19	CD19 antigen	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1319229	Cd19	CD19 antigen	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:15908920
1319229	Cd19	CD19 antigen	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723217
1319229	Cd19	CD19 antigen	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0009318	increased splenic marginal zone lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0009319	increased small lymphocytic lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174151
1319229	Cd19	CD19 antigen	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21341261
1319229	Cd19	CD19 antigen	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0009623	enlarged inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120817
1319229	Cd19	CD19 antigen	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1319229	Cd19	CD19 antigen	gene	MP:0009921	abnormal transitional stage T3 B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20156974
1319229	Cd19	CD19 antigen	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24242374
1319229	Cd19	CD19 antigen	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20156974
1319229	Cd19	CD19 antigen	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467694
1319229	Cd19	CD19 antigen	gene	MP:0010138	arteritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1319229	Cd19	CD19 antigen	gene	MP:0010228	decreased transitional stage T3 B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0010274	increased organ/body region tumor incidence		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1319229	Cd19	CD19 antigen	gene	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22341446
1319229	Cd19	CD19 antigen	gene	MP:0010336	increased acute lymphoblastic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930766
1319229	Cd19	CD19 antigen	gene	MP:0010337	increased chronic lymphocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174151
1319229	Cd19	CD19 antigen	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:23619366
1319229	Cd19	CD19 antigen	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1319229	Cd19	CD19 antigen	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1319229	Cd19	CD19 antigen	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174151
1319229	Cd19	CD19 antigen	gene	MP:0013940	abnormal plasmablast number		IAGP		N	RGD:5509061	20170921	MGI			PMID:26668357
1319229	Cd19	CD19 antigen	gene	MP:0013940	abnormal plasmablast number		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1319229	Cd19	CD19 antigen	gene	MP:0013940	abnormal plasmablast number		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1319229	Cd19	CD19 antigen	gene	MP:0014050	increased B cell acute lymphoblastic leukemia incidence		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1319229	Cd19	CD19 antigen	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21339646
1319229	Cd19	CD19 antigen	gene	MP:0014347	increased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:18490492
1319229	Cd19	CD19 antigen	gene	MP:0014348	decreased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:21795747
1319229	Cd19	CD19 antigen	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319229	Cd19	CD19 antigen	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1319229	Cd19	CD19 antigen	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1319229	Cd19	CD19 antigen	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:17513743
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230406	MGI			PMID:32209662
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20230406	MGI			PMID:32209662
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0010096	abnormal incisor color		IEA		N	RGD:5509061	20230601	MGI			
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0012216	decreased plasmalogen level		IAGP		N	RGD:5509061	20230406	MGI			PMID:32209662
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0012216	decreased plasmalogen level		IAGP		N	RGD:5509061	20240808	MGI			PMID:36690320
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0012218	decreased brain plasmalogen level		IAGP		N	RGD:5509061	20230406	MGI			PMID:32209662
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0012218	decreased brain plasmalogen level		IAGP		N	RGD:5509061	20240808	MGI			PMID:36690320
1319239	Peds1	plasmanylethanolamine desaturase 1	gene	MP:0012220	abnormal ether lipid level		IAGP		N	RGD:5509061	20240808	MGI			PMID:36690320
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19699733
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20211104	MGI			PMID:22109522
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:22109522
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20211104	MGI			PMID:22109522
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20211104	MGI			PMID:22109522
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0004266	pale placenta		IAGP		N	RGD:5509061	20211104	MGI			PMID:22109522
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0004560	abnormal chorionic plate morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:22109522
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:22109522
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19699733
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20211104	MGI			PMID:22109522
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319243	Bcl9l	B cell CLL/lymphoma 9-like	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:19699733
1319247	Ptk6	PTK6 protein tyrosine kinase 6	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782882
1319247	Ptk6	PTK6 protein tyrosine kinase 6	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20181227	MGI			
1319247	Ptk6	PTK6 protein tyrosine kinase 6	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782882
1319247	Ptk6	PTK6 protein tyrosine kinase 6	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782882
1319249	Dnal4	dynein, axonemal, light chain 4	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20210826	MGI			
1319249	Dnal4	dynein, axonemal, light chain 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1319249	Dnal4	dynein, axonemal, light chain 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201231	MGI			
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0004472	broad nasal bone		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20200402	MGI			
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0010832	lethality during fetal growth through weaning		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0030166	increased inner canthal distance		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0030280	short parietal bone		IAGP		N	RGD:5509061	20190718	MGI			PMID:30442762
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0030384	short facial bone		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319251	Lztr1	leucine-zipper-like transcriptional regulator, 1	gene	MP:0031152	subcutaneous hemorrhage		IAGP		N	RGD:5509061	20250410	MGI			PMID:39352760
1319253	Cep68	centrosomal protein 68	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1319253	Cep68	centrosomal protein 68	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1319253	Cep68	centrosomal protein 68	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220519	MGI			
1319255	Trappc8	trafficking protein particle complex 8	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20240523	MGI			
1319255	Trappc8	trafficking protein particle complex 8	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1319255	Trappc8	trafficking protein particle complex 8	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1319255	Trappc8	trafficking protein particle complex 8	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1319255	Trappc8	trafficking protein particle complex 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0004264	abnormal extraembryonic tissue physiology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0012681	collapsed brain ventricles		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0013227	small brain ventricles		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0014260	embryonic lethality prior to organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0020252	abnormal collagen level		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1319256	Sec23a	SEC23 homolog A, COPII coat complex component	gene	MP:0020413	increased amnion apoptosis		IAGP		N	RGD:5509061	20170223	MGI			PMID:26494538
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20210128	MGI			
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1319258	1700025G04Rik	RIKEN cDNA 1700025G04 gene	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1319260	Cox20	cytochrome c oxidase assembly protein 20	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20181227	MGI			
1319260	Cox20	cytochrome c oxidase assembly protein 20	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20181227	MGI			
1319260	Cox20	cytochrome c oxidase assembly protein 20	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20240523	MGI			
1319260	Cox20	cytochrome c oxidase assembly protein 20	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1319260	Cox20	cytochrome c oxidase assembly protein 20	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1319260	Cox20	cytochrome c oxidase assembly protein 20	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000381	enlarged hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001202	skin photosensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150924	MGI			PMID:25951169
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20150924	MGI			PMID:25951169
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25951169
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20150924	MGI			PMID:25951169
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001588	abnormal hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20150924	MGI			PMID:25951169
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0001928	abnormal ovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002879	increased cellular sensitivity to X-ray irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174697
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20150924	MGI			PMID:25951169
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0010202	focal dorsal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20150924	MGI			PMID:25951169
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9651581
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0010699	dilated hair follicle		IAGP		N	RGD:5509061	20181129	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16904611
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114557
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11950998
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17020410
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9426063
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20150924	MGI			PMID:25951169
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20150924	MGI			PMID:25951169
1319265	Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2	gene	MP:0031345	developmental cataract		IAGP		N	RGD:5509061	20220217	MGI			PMID:25951169
1319268	Rab24	RAB24, member RAS oncogene family	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1319268	Rab24	RAB24, member RAS oncogene family	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20240523	MGI			
1319268	Rab24	RAB24, member RAS oncogene family	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20170105	MGI			
1319268	Rab24	RAB24, member RAS oncogene family	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1319268	Rab24	RAB24, member RAS oncogene family	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160421	MGI			
1319268	Rab24	RAB24, member RAS oncogene family	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1319270	Hoxb13	homeobox B13	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0002758	long tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0002809	increased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668621
1319270	Hoxb13	homeobox B13	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0009380	abnormal prostate gland ventral lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668621
1319270	Hoxb13	homeobox B13	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12679105
1319270	Hoxb13	homeobox B13	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485650
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239451
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387736
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468431
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934575
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9639496
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934575
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387736
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9639496
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934575
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485650
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22042698
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22042698
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210805	MGI			
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210805	MGI			
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989983
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934575
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0002414	abnormal myeloblast morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9639496
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9639496
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387736
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0002620	abnormal monocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934575
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8934575
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485650
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239451
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22042698
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485650
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387736
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22042698
1319272	Csf3r	colony stimulating factor 3 receptor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210805	MGI			
1319276	Mrps2	mitochondrial ribosomal protein S2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20260402	MGI			
1319276	Mrps2	mitochondrial ribosomal protein S2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20160804	MGI			
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20160804	MGI			
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0010997	decreased aorta wall thickness		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0011642	abnormal bone collagen fibril morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319280	Fkbp10	FK506 binding protein 10	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24777781
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20241121	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20201022	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20221215	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0012559	decreased forebrain volume		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1319282	Ppil1	peptidylprolyl isomerase (cyclophilin)-like 1	gene	MP:0020602	decreased cerebral cortex average cell area		IAGP		N	RGD:5509061	20210325	MGI			PMID:33220177
1319286	Hspb9	heat shock protein family B (small) member 9	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1319286	Hspb9	heat shock protein family B (small) member 9	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0001391	abnormal tail movements		IEA		N	RGD:5509061	20141003	MGI			
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0001867	rhinitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0001947	abnormal mucociliary clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498047
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0001950	abnormal respiratory sounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498047
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498047
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498047
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498047
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498047
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:20442420
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0030118	rhinosinusitis		IAGP		N	RGD:5509061	20210211	MGI			PMID:20498047
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0030706	increased glutamine level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0030712	increased isoleucine level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0030724	increased valine level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0030732	increased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0030736	increased glutamic acid level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0030747	increased leucine level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37238654
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0031088	coughing		IAGP		N	RGD:5509061	20210211	MGI			PMID:20498047
1319290	Ttll1	tubulin tyrosine ligase-like 1	gene	MP:0031089	sneezing		IAGP		N	RGD:5509061	20210211	MGI			PMID:20498047
1319295	Fbxl16	F-box and leucine-rich repeat protein 16	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319299	Ndufb8	NADH:ubiquinone oxidoreductase subunit B8	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319299	Ndufb8	NADH:ubiquinone oxidoreductase subunit B8	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319299	Ndufb8	NADH:ubiquinone oxidoreductase subunit B8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832087
1319301	Cert1	ceramide transporter 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319301	Cert1	ceramide transporter 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0002237	abnormal nasal cavity morphology		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0002428	abnormal semicircular canal morphology		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0002728	absent tibia		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0003078	aphakia		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0004201	fetal growth retardation		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319301	Cert1	ceramide transporter 1	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0004612	fusion of vertebral bodies		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0004646	decreased cervical vertebrae number		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319301	Cert1	ceramide transporter 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20240711	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319301	Cert1	ceramide transporter 1	gene	MP:0008922	abnormal cervical rib		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0010496	abnormal pectinate muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0010572	persistent right dorsal aorta		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139267
1319301	Cert1	ceramide transporter 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319301	Cert1	ceramide transporter 1	gene	MP:0013247	placenta necrosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319301	Cert1	ceramide transporter 1	gene	MP:0013985	abnormal umbilical vein topology		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1319301	Cert1	ceramide transporter 1	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:29539633
1319301	Cert1	ceramide transporter 1	gene	MP:0031594	increased cardiac jelly amount		IAGP		N	RGD:5509061	20240229	MGI			PMID:19139267
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:30135927
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0002891	increased insulin sensitivity		IEA		N	RGD:5509061	20170817	MGI			
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0004889	increased energy expenditure		IEA		N	RGD:5509061	20170817	MGI			
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20170817	MGI			PMID:21552327
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0005439	decreased glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191128	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20191128	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0014063	Lafora bodies		IAGP		N	RGD:5509061	20230601	MGI			PMID:30135927
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0014072	decreased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20191128	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0030021	increased muscle cell glucose uptake		IEA		N	RGD:5509061	20170817	MGI			
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0030994	decreased adipose tissue glycogen level		IAGP		N	RGD:5509061	20191128	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:12727934
1319303	Ppp1r3c	protein phosphatase 1, regulatory subunit 3C	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:12727934
1319305	Pkp3	plakophilin 3	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0000405	abnormal auchene hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0000424	retarded hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0003846	matted coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0008768	abnormal hair medulla air spaces		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0010234	abnormal vibrissa follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18079750
1319305	Pkp3	plakophilin 3	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20181129	MGI			PMID:18079750
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539463
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173597
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173597
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220811	MGI			
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173597
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539463
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173597
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539463
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539463
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20210211	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20210211	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0003537	hydrometrocolpos		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20191128	MGI			PMID:31479441
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005195	abnormal posterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20210211	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539463
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005633	increased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539463
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0006357	abnormal circulating mineral level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032602
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173597
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20191128	MGI			PMID:31479441
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20191128	MGI			PMID:31479441
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173597
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173597
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539463
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20210211	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0010092	increased circulating magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519557
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322545
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15173597
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0011281	abnormal olfactory epithelium cilium morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:15322545
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20210211	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170202	MGI			PMID:16794820
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20191128	MGI			PMID:31479441
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0020511	decreased dendritic spine length		IAGP		N	RGD:5509061	20191128	MGI			PMID:31479441
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20191128	MGI			PMID:31479441
1319307	Bbs4	Bardet-Biedl syndrome 4	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:15173597
1319310	Nrn1l	neuritin 1-like	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1319310	Nrn1l	neuritin 1-like	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220519	MGI			
1319310	Nrn1l	neuritin 1-like	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20201210	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20200310	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240613	MGI			PMID:38697008
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20201210	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20201210	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0010738	abnormal internode morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0010738	abnormal internode morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0011730	increased myelin sheath thickness		IAGP		N	RGD:5509061	20201210	MGI			PMID:31199454
1319313	Cfap276	cilia and flagella associated protein 276	gene	MP:0011730	increased myelin sheath thickness		IAGP		N	RGD:5509061	20201210	MGI			PMID:32592472
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20221215	MGI			
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765887
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247420
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765887
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765887
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0001784	abnormal fluid regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765887
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247420
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247420
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23722907
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765887
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19381288
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247420
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20230601	MGI			
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765887
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23722907
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247420
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20230601	MGI			
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20260402	MGI			
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247420
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765887
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247420
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765887
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011304	kidney papillary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011332	abnormal kidney outer medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011378	abnormal kidney outer medulla inner stripe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:21765887
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983020
1319319	Nfat5	nuclear factor of activated T cells 5	gene	MP:0012007	abnormal chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23722907
1319321	Dlk2	delta like non-canonical Notch ligand 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20201029	MGI			PMID:28863347
1319321	Dlk2	delta like non-canonical Notch ligand 2	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20201029	MGI			PMID:28863347
1319321	Dlk2	delta like non-canonical Notch ligand 2	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20201029	MGI			PMID:28863347
1319321	Dlk2	delta like non-canonical Notch ligand 2	gene	MP:0014414	increased depression-related behavior		IAGP		N	RGD:5509061	20240425	MGI			PMID:28863347
1319322	Thnsl2	threonine synthase-like 2 (bacterial)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20231207	MGI			
1319322	Thnsl2	threonine synthase-like 2 (bacterial)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1319322	Thnsl2	threonine synthase-like 2 (bacterial)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1319322	Thnsl2	threonine synthase-like 2 (bacterial)	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1319322	Thnsl2	threonine synthase-like 2 (bacterial)	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1319334	Jade2	jade family PHD finger 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1319334	Jade2	jade family PHD finger 2	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210826	MGI			
1319334	Jade2	jade family PHD finger 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210826	MGI			
1319334	Jade2	jade family PHD finger 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20240822	MGI			PMID:36008159
1319334	Jade2	jade family PHD finger 2	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20240822	MGI			PMID:36008159
1319334	Jade2	jade family PHD finger 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1319334	Jade2	jade family PHD finger 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20240822	MGI			PMID:36008159
1319334	Jade2	jade family PHD finger 2	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20240822	MGI			PMID:36008159
1319334	Jade2	jade family PHD finger 2	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20240822	MGI			PMID:36008159
1319334	Jade2	jade family PHD finger 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200514	MGI			
1319334	Jade2	jade family PHD finger 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1319334	Jade2	jade family PHD finger 2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1319334	Jade2	jade family PHD finger 2	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20200514	MGI			
1319334	Jade2	jade family PHD finger 2	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240822	MGI			PMID:36008159
1319334	Jade2	jade family PHD finger 2	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240822	MGI			PMID:36008159
1319334	Jade2	jade family PHD finger 2	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20240822	MGI			PMID:36008159
1319336	Smyd5	SET and MYND domain containing 5	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20240926	MGI			PMID:35643234
1319336	Smyd5	SET and MYND domain containing 5	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1319336	Smyd5	SET and MYND domain containing 5	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20240926	MGI			PMID:35643234
1319337	Cst7	cystatin F (leukocystatin)	gene	MP:0002148	abnormal hypersensitivity reaction		IAGP		N	RGD:5509061	20250220	MGI			PMID:27067058
1319337	Cst7	cystatin F (leukocystatin)	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1319337	Cst7	cystatin F (leukocystatin)	gene	MP:0002465	abnormal eosinophil physiology		IAGP		N	RGD:5509061	20250220	MGI			PMID:27067058
1319337	Cst7	cystatin F (leukocystatin)	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20250220	MGI			PMID:27067058
1319337	Cst7	cystatin F (leukocystatin)	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20250220	MGI			PMID:27067058
1319337	Cst7	cystatin F (leukocystatin)	gene	MP:0005061	abnormal eosinophil morphology		IAGP		N	RGD:5509061	20250220	MGI			PMID:27067058
1319337	Cst7	cystatin F (leukocystatin)	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20250220	MGI			PMID:27067058
1319337	Cst7	cystatin F (leukocystatin)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20250220	MGI			PMID:27067058
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20181227	MGI			
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935478
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935478
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20210128	MGI			
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319339	Fkbp5	FK506 binding protein 5	gene	MP:0014413	decreased depression-related behavior		IAGP		N	RGD:5509061	20240425	MGI			PMID:21935478
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11892011
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20150625	MGI			PMID:10328999
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000592	short tail		IEA		N	RGD:5509061	20111116	MGI			
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:14169723
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245024
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20150611	MGI			PMID:20506478
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245024
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14169723
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245024
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:2051161
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20150611	MGI			PMID:20506478
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245024
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757819
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245024
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150611	MGI			PMID:20506478
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20150611	MGI			PMID:20506478
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11892011
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14169723
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201022	MGI			PMID:15148410
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757819
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20201022	MGI			PMID:15148410
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245024
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20111116	MGI			
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245024
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20111116	MGI			
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757819
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148410
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14169723
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20150611	MGI			PMID:20506478
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11892011
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0003492	abnormal involuntary movement		IEA		N	RGD:5509061	20111116	MGI			
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0003871	abnormal myelin sheath morphology		IEA		N	RGD:5509061	20111116	MGI			
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0004077	abnormal striatum morphology		IEA		N	RGD:5509061	20111116	MGI			
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0004814	reduced linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20150625	MGI			PMID:10328999
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11892011
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0006057	decreased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16245024
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20150625	MGI			PMID:10328999
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757819
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757819
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757819
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14169723
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0010734	abnormal paranode morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:20506478
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011086	postnatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20150625	MGI			PMID:10328999
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410318
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11892011
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706070
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470614
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20150625	MGI			PMID:10328999
1319347	Qki	quaking, KH domain containing RNA binding	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20150611	MGI			PMID:20506478
1319349	Gpr155	G protein-coupled receptor 155	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1319349	Gpr155	G protein-coupled receptor 155	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20210128	MGI			
1319349	Gpr155	G protein-coupled receptor 155	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1319349	Gpr155	G protein-coupled receptor 155	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1319349	Gpr155	G protein-coupled receptor 155	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1319349	Gpr155	G protein-coupled receptor 155	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1319354	Cldn14	claudin 14	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913076
1319354	Cldn14	claudin 14	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913076
1319354	Cldn14	claudin 14	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913076
1319354	Cldn14	claudin 14	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913076
1319354	Cldn14	claudin 14	gene	MP:0004530	absent outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913076
1319354	Cldn14	claudin 14	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913076
1319354	Cldn14	claudin 14	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913076
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11894097
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691841
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11894098
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11894097
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11894098
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11894098
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11894097
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11894098
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11894097
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11894098
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1319358	Ripk2	receptor (TNFRSF)-interacting serine-threonine kinase 2	gene	MP:0012564	decreased tumor incidence following infection		IAGP		N	RGD:5509061	20241114	MGI			PMID:36103821
1319360	Trim45	tripartite motif-containing 45	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0003078	aphakia		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0010484	bicuspid aortic valve		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1319360	Trim45	tripartite motif-containing 45	gene	MP:0014003	additional anastomosis between intracranial vertebral arteries		IEA		N	RGD:5509061	20170504	MGI			
1319362	4930579F01Rik	RIKEN cDNA 4930579F01 gene	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1319362	4930579F01Rik	RIKEN cDNA 4930579F01 gene	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20240523	MGI			
1319363	Kif18a	kinesin family member 18A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20151126	MGI			PMID:12855593
1319363	Kif18a	kinesin family member 18A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20151126	MGI			PMID:12855593
1319363	Kif18a	kinesin family member 18A	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20151126	MGI			PMID:12855593
1319363	Kif18a	kinesin family member 18A	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20151126	MGI			PMID:12855593
1319363	Kif18a	kinesin family member 18A	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20250206	MGI			PMID:37795949
1319363	Kif18a	kinesin family member 18A	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0009564	abnormal meiotic configurations		IAGP		N	RGD:5509061	20250206	MGI			PMID:37795949
1319363	Kif18a	kinesin family member 18A	gene	MP:0009566	meiotic nondisjunction		IAGP		N	RGD:5509061	20250206	MGI			PMID:37795949
1319363	Kif18a	kinesin family member 18A	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151126	MGI			PMID:16822657
1319363	Kif18a	kinesin family member 18A	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20160623	MGI			PMID:25824710
1319363	Kif18a	kinesin family member 18A	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:20981276
1319363	Kif18a	kinesin family member 18A	gene	MP:0031020	premature ovarian failure		IAGP		N	RGD:5509061	20200130	MGI			PMID:16822657
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0003155	abnormal telomere length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319365	Ctc1	CTS telomere maintenance complex component 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22531781
1319367	Rgr	retinal G protein coupled receptor	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431696
1319367	Rgr	retinal G protein coupled receptor	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431696
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0020427	increased hepatocyte karyomegaly		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319369	Mad2l1bp	MAD2L1 binding protein	gene	MP:0030951	abnormal endocytosis		IAGP		N	RGD:5509061	20211118	MGI			PMID:27374329
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0001192	scaly skin		IEA		N	RGD:5509061	20141003	MGI			
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0001255	decreased body height		IEA		N	RGD:5509061	20141003	MGI			
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20141003	MGI			
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20150108	MGI			
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319371	Erp44	endoplasmic reticulum protein 44	gene	MP:0031645	increased myocardial fiber apoptosis		IAGP		N	RGD:5509061	20260806	MGI			PMID:25332179
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618285
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618285
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618285
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618285
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618285
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0009641	kidney degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618285
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0011363	renal glomerulus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0011422	kidney medulla atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618285
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0011423	kidney cortex atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618285
1319372	Glis2	GLIS family zinc finger 2	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:18227149
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0002892	decreased superior colliculus size		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0003246	loss of GABAergic neurons		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0009038	decreased inferior colliculus size		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0009960	abnormal cerebellum anterior lobe morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483223
1319374	Upf2	UPF2 regulator of nonsense transcripts homolog (yeast)	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1319376	Hoxd1	homeobox D1	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:21151121
1319376	Hoxd1	homeobox D1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21151121
1319376	Hoxd1	homeobox D1	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21151121
1319376	Hoxd1	homeobox D1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11511348
1319376	Hoxd1	homeobox D1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11511348
1319376	Hoxd1	homeobox D1	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11511348
1319376	Hoxd1	homeobox D1	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:11511348
1319376	Hoxd1	homeobox D1	gene	MP:0010729	absent arcus anterior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11511348
1319376	Hoxd1	homeobox D1	gene	MP:0010730	absent odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:11511348
1319376	Hoxd1	homeobox D1	gene	MP:0014488	abnormal skin sensory neuron innervation pattern		IAGP		N	RGD:5509061	20240801	MGI			PMID:21151121
1319380	Shc4	SHC (Src homology 2 domain containing) family, member 4	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1319382	Anks1	ankyrin repeat and SAM domain containing 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20221215	MGI			
1319382	Anks1	ankyrin repeat and SAM domain containing 1	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20221215	MGI			
1319382	Anks1	ankyrin repeat and SAM domain containing 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20230601	MGI			
1319382	Anks1	ankyrin repeat and SAM domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20100865
1319382	Anks1	ankyrin repeat and SAM domain containing 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1319382	Anks1	ankyrin repeat and SAM domain containing 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1319382	Anks1	ankyrin repeat and SAM domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1319382	Anks1	ankyrin repeat and SAM domain containing 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1319387	Mastl	microtubule associated serine/threonine kinase-like	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24101512
1319387	Mastl	microtubule associated serine/threonine kinase-like	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24101512
1319387	Mastl	microtubule associated serine/threonine kinase-like	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24101512
1319387	Mastl	microtubule associated serine/threonine kinase-like	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24101512
1319387	Mastl	microtubule associated serine/threonine kinase-like	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24101512
1319389	Bri3	brain protein I3	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201231	MGI			
1319393	Msh4	mutS homolog 4	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1319393	Msh4	mutS homolog 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1319393	Msh4	mutS homolog 4	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1319393	Msh4	mutS homolog 4	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1319393	Msh4	mutS homolog 4	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1319393	Msh4	mutS homolog 4	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1319393	Msh4	mutS homolog 4	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1319393	Msh4	mutS homolog 4	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0005134	decreased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20160714	MGI			PMID:18272476
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20160714	MGI			PMID:18272476
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20171012	MGI			PMID:26232227
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150924	MGI			PMID:26232227
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22644989
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:15248865
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:26232227
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:15248865
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:15248865
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:15248865
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0020474	advanced circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:15248865
1319400	Zfhx3	zinc finger homeobox 3	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20171012	MGI			PMID:15248865
1319402	Malt1	MALT1 paracaspase	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20201022	MGI			PMID:32343482
1319402	Malt1	MALT1 paracaspase	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576442
1319402	Malt1	MALT1 paracaspase	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20201022	MGI			PMID:32343482
1319402	Malt1	MALT1 paracaspase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20201022	MGI			PMID:32343482
1319402	Malt1	MALT1 paracaspase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:32343482
1319402	Malt1	MALT1 paracaspase	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614861
1319402	Malt1	MALT1 paracaspase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614861
1319402	Malt1	MALT1 paracaspase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576442
1319402	Malt1	MALT1 paracaspase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576442
1319402	Malt1	MALT1 paracaspase	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576442
1319402	Malt1	MALT1 paracaspase	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862125
1319402	Malt1	MALT1 paracaspase	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576442
1319402	Malt1	MALT1 paracaspase	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576442
1319402	Malt1	MALT1 paracaspase	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20201022	MGI			PMID:32343482
1319402	Malt1	MALT1 paracaspase	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576442
1319402	Malt1	MALT1 paracaspase	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614861
1319402	Malt1	MALT1 paracaspase	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20201022	MGI			PMID:32343482
1319402	Malt1	MALT1 paracaspase	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576442
1319402	Malt1	MALT1 paracaspase	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576442
1319402	Malt1	MALT1 paracaspase	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20150702	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000140	absent vertebral pedicles		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000153	rib bifurcation		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000161	scoliosis		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000297	abnormal atrioventricular cushion morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000489	abnormal large intestine morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000534	abnormal ureter morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0003345	decreased rib number		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0004442	occipital bone foramen		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0004646	decreased cervical vertebrae number		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0013913	absent costovertebral joint		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0013914	absent intracranial segment of vertebral artery		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0014003	additional anastomosis between intracranial vertebral arteries		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1319407	Cirsr	corepressor of RBPJ and splicing regulator	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1319411	Kcnk16	potassium channel, subfamily K, member 16	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20180503	MGI			PMID:28928238
1319411	Kcnk16	potassium channel, subfamily K, member 16	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20180503	MGI			PMID:28928238
1319411	Kcnk16	potassium channel, subfamily K, member 16	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1319411	Kcnk16	potassium channel, subfamily K, member 16	gene	MP:0013277	abnormal fasting circulating glucose level		IAGP		N	RGD:5509061	20180503	MGI			PMID:28928238
1319415	Phc1	polyhomeotic 1	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0000080	abnormal exoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11901201
1319415	Phc1	polyhomeotic 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20170817	MGI			PMID:11950896
1319415	Phc1	polyhomeotic 1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122109
1319415	Phc1	polyhomeotic 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11901201
1319415	Phc1	polyhomeotic 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20170817	MGI			PMID:11950896
1319415	Phc1	polyhomeotic 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11901201
1319415	Phc1	polyhomeotic 1	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122109
1319415	Phc1	polyhomeotic 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0003494	parathyroid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0004441	small occipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11901201
1319415	Phc1	polyhomeotic 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122109
1319415	Phc1	polyhomeotic 1	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20170817	MGI			PMID:11950896
1319415	Phc1	polyhomeotic 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20170817	MGI			PMID:11950896
1319415	Phc1	polyhomeotic 1	gene	MP:0010428	abnormal heart right ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0010458	pulmonary trunk hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0010568	abnormal bulbus cordis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122109
1319415	Phc1	polyhomeotic 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0012062	small tail bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024804
1319415	Phc1	polyhomeotic 1	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:9367423
1319415	Phc1	polyhomeotic 1	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:9367423
1319418	Ccnt2	cyclin T2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1319418	Ccnt2	cyclin T2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1319418	Ccnt2	cyclin T2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
1319418	Ccnt2	cyclin T2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1319418	Ccnt2	cyclin T2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19364821
1319418	Ccnt2	cyclin T2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319418	Ccnt2	cyclin T2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16129705
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1319422	Ppp2r3c	protein phosphatase 2, regulatory subunit B'', gamma	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1319425	Ccni	cyclin I	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847066
1319425	Ccni	cyclin I	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847066
1319425	Ccni	cyclin I	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847066
1319425	Ccni	cyclin I	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847066
1319425	Ccni	cyclin I	gene	MP:0011282	increased podocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847066
1319425	Ccni	cyclin I	gene	MP:0011369	increased renal glomerulus apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847066
1319425	Ccni	cyclin I	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847066
1319427	Grtp1	GH regulated TBC protein 1	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20160811	MGI			
1319427	Grtp1	GH regulated TBC protein 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20160811	MGI			
1319427	Grtp1	GH regulated TBC protein 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1319427	Grtp1	GH regulated TBC protein 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1319428	Cdt1	chromatin licensing and DNA replication factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151217	MGI			PMID:23817338
1319433	Rars1	arginyl-tRNA synthetase 1	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20160804	MGI			
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281280
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18196599
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18196599
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18196599
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807321
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18196599
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18196599
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18196599
1319438	Hs6st1	heparan sulfate 6-O-sulfotransferase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17405882
1319439	Ctdspl2	CTD small phosphatase like 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1319439	Ctdspl2	CTD small phosphatase like 2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1319439	Ctdspl2	CTD small phosphatase like 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1319439	Ctdspl2	CTD small phosphatase like 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20240801	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20240801	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20240801	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20240801	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20241017	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20240801	MGI			PMID:38769918
1319440	Kansl3	KAT8 regulatory NSL complex subunit 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23219391
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20111116	MGI			
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20111116	MGI			
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12065839
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9885898
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751756
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12065839
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843989
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20150618	MGI			PMID:15655112
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0002064	seizures		IEA		N	RGD:5509061	20111116	MGI			
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751756
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878135
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12065839
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0004918	abnormal negative T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751756
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391195
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23219391
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9885898
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843989
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843989
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9885898
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0006413	increased T cell apoptosis		IEA		N	RGD:5509061	20111116	MGI			
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843989
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18209052
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9885898
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20190606	MGI			
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391195
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0009787	increased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23219391
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267019
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0010336	increased acute lymphoblastic leukemia incidence		IAGP		N	RGD:5509061	20150618	MGI			PMID:15655112
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1319443	Cd3e	CD3 antigen, epsilon polypeptide	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190606	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20240523	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20260402	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20241121	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20241121	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20241121	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1319445	Gng12	guanine nucleotide binding protein (G protein), gamma 12	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1319449	Eif4a2	eukaryotic translation initiation factor 4A2	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20241121	MGI			
1319449	Eif4a2	eukaryotic translation initiation factor 4A2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20240523	MGI			
1319449	Eif4a2	eukaryotic translation initiation factor 4A2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1319449	Eif4a2	eukaryotic translation initiation factor 4A2	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1319449	Eif4a2	eukaryotic translation initiation factor 4A2	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20250508	MGI			
1319449	Eif4a2	eukaryotic translation initiation factor 4A2	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20241121	MGI			
1319449	Eif4a2	eukaryotic translation initiation factor 4A2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0000129	ameloblast degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20241121	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0003883	enlarged stomach		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0003948	abnormal gas homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20240523	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20241121	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0009131	decreased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20170608	MGI			PMID:26880786
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19187773
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0013249	adipose tissue necrosis		IAGP		N	RGD:5509061	20161117	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0030542	abnormal dentin development		IAGP		N	RGD:5509061	20180215	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0030827	femur fracture		IAGP		N	RGD:5509061	20181018	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21051554
1319454	Agpat2	1-acylglycerol-3-phosphate O-acyltransferase 2	gene	MP:0031603	brown adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:21051554
1319456	Wdr33	WD repeat domain 33	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1319456	Wdr33	WD repeat domain 33	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230119	MGI			
1319456	Wdr33	WD repeat domain 33	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1319456	Wdr33	WD repeat domain 33	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469594
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0003943	abnormal hepatobiliary system development		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004420	parietal bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004455	pterygoid bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004461	basisphenoid bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004473	absent nasal bone		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940357
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0005123	increased circulating growth hormone level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0008023	abnormal styloid process morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940357
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940357
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0008991	abnormal bile canaliculus morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469594
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0009891	abnormal palate bone morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0009913	abnormal hyoid bone greater horn morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141218	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469594
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0012090	midbrain hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0012129	failure of blastocyst formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10469594
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0012139	increased forebrain size		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:23299886
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030112	zygomatic bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030119	abnormal retrotympanic process morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030261	abnormal temporal bone zygomatic process morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030285	mandibular coronoid process hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030301	abnormal maxillary frontal process morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030374	Meckel's cartilage hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030386	facial bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030869	thyroid cartilage hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0030874	cricoid cartilage hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0031454	decreased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20221110	MGI			PMID:34184034
1319460	Srsf3	serine and arginine-rich splicing factor 3	gene	MP:0031459	maxillary zygomatic process hypoplasia		IAGP		N	RGD:5509061	20221201	MGI			PMID:34184034
1319462	Uap1	UDP-N-acetylglucosamine pyrophosphorylase 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230119	MGI			
1319462	Uap1	UDP-N-acetylglucosamine pyrophosphorylase 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1319462	Uap1	UDP-N-acetylglucosamine pyrophosphorylase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1319462	Uap1	UDP-N-acetylglucosamine pyrophosphorylase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1319464	Zc3hav1l	zinc finger CCCH-type, antiviral 1-like	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20181227	MGI			
1319464	Zc3hav1l	zinc finger CCCH-type, antiviral 1-like	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1319464	Zc3hav1l	zinc finger CCCH-type, antiviral 1-like	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1319466	Tle1	transducin-like enhancer of split 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1319466	Tle1	transducin-like enhancer of split 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20240523	MGI			
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748127
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748127
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319471	Spmap2	sperm microtubule associated protein 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10747865
1319472	Eif1b	eukaryotic translation initiation factor 1B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1319472	Eif1b	eukaryotic translation initiation factor 1B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1319474	Rnmt	RNA (guanine-7-) methyltransferase	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1319474	Rnmt	RNA (guanine-7-) methyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319474	Rnmt	RNA (guanine-7-) methyltransferase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1319474	Rnmt	RNA (guanine-7-) methyltransferase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1319476	Calr3	calreticulin 3	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131354
1319476	Calr3	calreticulin 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131354
1319476	Calr3	calreticulin 3	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20200102	MGI			PMID:21131354
1319476	Calr3	calreticulin 3	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220303	MGI			PMID:21131354
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20141009	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20200402	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20141003	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20141003	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20141003	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20160114	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20160114	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20170105	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20160114	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201231	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20201231	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319478	Agap1	ArfGAP with GTPase domain, ankyrin repeat and PH domain 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20201231	MGI			
1319480	Unc5d	unc-5 netrin receptor D	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673655
1319480	Unc5d	unc-5 netrin receptor D	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673655
1319484	Tjp3	tight junction protein 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17000770
1319484	Tjp3	tight junction protein 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18172007
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0010656	thick myocardium		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0014390	decreased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0014906	abnormal muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:35803927
1319486	Sdhaf4	succinate dehydrogenase complex assembly factor 4	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:35803927
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200042
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801644
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200042
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801644
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200042
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200042
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801644
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0008109	abnormal small intestinal microvillus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801644
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801644
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801644
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801644
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200042
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801644
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0011198	absent proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200042
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20150611	MGI			PMID:25660120
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200042
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:18200042
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0014079	decreased small intestinal villus number		IAGP		N	RGD:5509061	20160414	MGI			PMID:19801644
1319488	Gadd45gip1	growth arrest and DNA-damage-inducible, gamma interacting protein 1	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20160414	MGI			PMID:19801644
1319490	Slc30a6	solute carrier family 30 (zinc transporter), member 6	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20260402	MGI			
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0020352	abnormal endoplasmic reticulum physiology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0020365	increased brain iron level		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319492	1600014C10Rik	RIKEN cDNA 1600014C10 gene	gene	MP:0031686	abnormal smooth endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41239414
1319495	Lzic	leucine zipper and CTNNBIP1 domain containing	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20241219	MGI			PMID:38950903
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20241219	MGI			PMID:38950903
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20241219	MGI			PMID:38950903
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20241219	MGI			PMID:38950903
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0003443	increased circulating glycerol level		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20241219	MGI			PMID:38950903
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0010092	increased circulating magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20241219	MGI			PMID:38950903
1319497	Trmt10a	tRNA methyltransferase 10A	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20241219	MGI			PMID:38950903
1319499	Zmiz2	zinc finger, MIZ-type containing 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1319499	Zmiz2	zinc finger, MIZ-type containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319499	Zmiz2	zinc finger, MIZ-type containing 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1319499	Zmiz2	zinc finger, MIZ-type containing 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1319505	Dnali1	dynein, axonemal, light intermediate polypeptide 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20231102	MGI			PMID:36792588
1319505	Dnali1	dynein, axonemal, light intermediate polypeptide 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20231102	MGI			PMID:36792588
1319505	Dnali1	dynein, axonemal, light intermediate polypeptide 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20231102	MGI			PMID:36792588
1319505	Dnali1	dynein, axonemal, light intermediate polypeptide 1	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20231102	MGI			PMID:36792588
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085069
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625273
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:21555557
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:21555557
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085069
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085069
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:21555557
1319507	Rce1	Ras converting CAAX endopeptidase 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:21555557
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20240523	MGI			
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20240523	MGI			
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1319510	Tmco6	transmembrane and coiled-coil domains 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228099
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228099
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20150521	MGI			PMID:22228099
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228099
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0004574	broad limb buds		IAGP		N	RGD:5509061	20150521	MGI			PMID:22228099
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210520	MGI			
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228099
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22228099
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0012531	delayed limb development		IAGP		N	RGD:5509061	20150521	MGI			PMID:22228099
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0030964	decreased brain ependyma motile cilium length		IAGP		N	RGD:5509061	20190725	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0030966	decreased brain ependyma motile cilium number		IAGP		N	RGD:5509061	20190725	MGI			PMID:23572516
1319512	Bbs7	Bardet-Biedl syndrome 7	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:23572516
1319515	Tmem131	transmembrane protein 131	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20220519	MGI			
1319515	Tmem131	transmembrane protein 131	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1319515	Tmem131	transmembrane protein 131	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220519	MGI			
1319515	Tmem131	transmembrane protein 131	gene	MP:0001785	edema		IEA		N	RGD:5509061	20220519	MGI			
1319515	Tmem131	transmembrane protein 131	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20220519	MGI			
1319515	Tmem131	transmembrane protein 131	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1319515	Tmem131	transmembrane protein 131	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1319515	Tmem131	transmembrane protein 131	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1319515	Tmem131	transmembrane protein 131	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1319517	Cstf1	cleavage stimulation factor, 3' pre-RNA, subunit 1	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20230601	MGI			
1319517	Cstf1	cleavage stimulation factor, 3' pre-RNA, subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319517	Cstf1	cleavage stimulation factor, 3' pre-RNA, subunit 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20250508	MGI			
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19815519
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000413	polyphalangy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056373
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000867	abnormal cerebellum anterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056373
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21337666
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698544
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21337666
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15215207
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20180927	MGI			PMID:29999500
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21337666
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20180927	MGI			PMID:29999500
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914490
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056373
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22549777
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28817564
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29999500
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003159	abnormal esophageal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003160	abnormal esophagus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056373
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004100	abnormal spinal cord interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004544	absent esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004711	persistence of notochord tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004711	persistence of notochord tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004791	absent lower incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0005315	absent pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0006097	abnormal cerebellar lobule formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19815519
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009004	progressive hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009199	abnormal external male genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009569	abnormal left lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009570	abnormal right lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009571	abnormal right lung accessory lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009572	abnormal right lung cranial lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950124
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010811	decreased type II pneumocyte number		IAGP		N	RGD:5509061	20180927	MGI			PMID:29999500
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010824	absent right lung accessory lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010827	small lung saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010828	abnormal bronchioalveolar stem cell morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29999500
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010881	esophagus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010882	trachea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010883	trachea stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010884	esophagus stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010885	absent trachea		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0010906	abnormal lung bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011011	impaired lung lobe morphogenesis		IAGP		N	RGD:5509061	20200917	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056373
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914490
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011148	decreased mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006072
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0013496	abnormal trachea development		IAGP		N	RGD:5509061	20150212	MGI			PMID:9731531
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0013785	abnormal mammary gland bud morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:16914490
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0021101	abnormal ventral interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0021101	abnormal ventral interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0021102	abnormal ventral interneuron 0 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0021103	abnormal ventral interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:11748151
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:12361967
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:14723851
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15215207
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0030255	abnormal maxillary dental arch morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:19056373
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0030258	small mandibular condyloid process		IAGP		N	RGD:5509061	20171019	MGI			PMID:19815519
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0030301	abnormal maxillary frontal process morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:19056373
1319523	Gli2	GLI-Kruppel family member GLI2	gene	MP:0030331	absent temporomandibular joint disk		IAGP		N	RGD:5509061	20171109	MGI			PMID:19815519
1319525	Kcnv2	potassium channel, subfamily V, member 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141030	MGI			
1319525	Kcnv2	potassium channel, subfamily V, member 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30820446
1319525	Kcnv2	potassium channel, subfamily V, member 2	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30820446
1319525	Kcnv2	potassium channel, subfamily V, member 2	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20200116	MGI			PMID:30820446
1319525	Kcnv2	potassium channel, subfamily V, member 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:30820446
1319525	Kcnv2	potassium channel, subfamily V, member 2	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:30820446
1319525	Kcnv2	potassium channel, subfamily V, member 2	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:30820446
1319525	Kcnv2	potassium channel, subfamily V, member 2	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20200116	MGI			PMID:30820446
1319525	Kcnv2	potassium channel, subfamily V, member 2	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20200116	MGI			PMID:30820446
1319526	Sall2	spalt like transcription factor 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818376
1319526	Sall2	spalt like transcription factor 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818376
1319526	Sall2	spalt like transcription factor 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818376
1319526	Sall2	spalt like transcription factor 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818376
1319526	Sall2	spalt like transcription factor 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1319526	Sall2	spalt like transcription factor 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150305	MGI			PMID:18818376
1319526	Sall2	spalt like transcription factor 2	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818376
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16144837
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0000371	diluted coat color		IEA		N	RGD:5509061	20111116	MGI			
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308543
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308543
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20201231	MGI			
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308543
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8699821
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16144837
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:8699821
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20210826	MGI			
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16144837
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308543
1319532	Slc7a11	solute carrier family 7 (cationic amino acid transporter, y+ system), member 11	gene	MP:0030625	increased circulating cysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:16144837
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191128	MGI			
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1319535	Mrpl22	mitochondrial ribosomal protein L22	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260716	MGI			PMID:32376682
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940150
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434326
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434326
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940150
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434326
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0004100	abnormal spinal cord interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434326
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434326
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0011019	abnormal adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434326
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434326
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434326
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434326
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467430
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940150
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0014386	decreased muscle fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:20940150
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0014390	decreased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:20940150
1319539	Tk2	thymidine kinase 2, mitochondrial	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20250911	MGI			PMID:18434326
1319541	Rfc5	replication factor C (activator 1) 5	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20230601	MGI			
1319541	Rfc5	replication factor C (activator 1) 5	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220519	MGI			
1319541	Rfc5	replication factor C (activator 1) 5	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220519	MGI			
1319541	Rfc5	replication factor C (activator 1) 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1319541	Rfc5	replication factor C (activator 1) 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20160811	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0000947	convulsive seizures		IEA		N	RGD:5509061	20201231	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20141003	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20201231	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20220519	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20170105	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20181227	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20210826	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20170105	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20220519	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20201231	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20190502	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0010571	shortened ST segment		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20260402	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20210128	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1319544	Rnf10	ring finger protein 10	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1319548	Gpn1	GPN-loop GTPase 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20240523	MGI			
1319548	Gpn1	GPN-loop GTPase 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241017	MGI			
1319548	Gpn1	GPN-loop GTPase 1	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1319548	Gpn1	GPN-loop GTPase 1	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1319548	Gpn1	GPN-loop GTPase 1	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1319548	Gpn1	GPN-loop GTPase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1319548	Gpn1	GPN-loop GTPase 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1319552	Ppp1r12b	protein phosphatase 1, regulatory subunit 12B	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20240502	MGI			PMID:38224947
1319552	Ppp1r12b	protein phosphatase 1, regulatory subunit 12B	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1319552	Ppp1r12b	protein phosphatase 1, regulatory subunit 12B	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20240502	MGI			PMID:36889588
1319552	Ppp1r12b	protein phosphatase 1, regulatory subunit 12B	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20240523	MGI			
1319552	Ppp1r12b	protein phosphatase 1, regulatory subunit 12B	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20240502	MGI			PMID:36889588
1319552	Ppp1r12b	protein phosphatase 1, regulatory subunit 12B	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20240502	MGI			PMID:36889588
1319552	Ppp1r12b	protein phosphatase 1, regulatory subunit 12B	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20240502	MGI			PMID:38224947
1319552	Ppp1r12b	protein phosphatase 1, regulatory subunit 12B	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20240502	MGI			PMID:36889588
1319552	Ppp1r12b	protein phosphatase 1, regulatory subunit 12B	gene	MP:0010580	decreased heart left ventricle size		IAGP		N	RGD:5509061	20240502	MGI			PMID:36889588
1319555	Nthl1	nth (endonuclease III)-like 1 (E.coli)	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1319555	Nthl1	nth (endonuclease III)-like 1 (E.coli)	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1319555	Nthl1	nth (endonuclease III)-like 1 (E.coli)	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
1319555	Nthl1	nth (endonuclease III)-like 1 (E.coli)	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
1319555	Nthl1	nth (endonuclease III)-like 1 (E.coli)	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20160804	MGI			PMID:12167705
1319555	Nthl1	nth (endonuclease III)-like 1 (E.coli)	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:12093749
1319557	Supt6	SPT6, histone chaperone and transcription elongation factor	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20151203	MGI			PMID:26142281
1319560	Nacc2	nucleus accumbens associated 2, BEN and BTB (POZ) domain containing	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20201231	MGI			
1319560	Nacc2	nucleus accumbens associated 2, BEN and BTB (POZ) domain containing	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201022	MGI			
1319560	Nacc2	nucleus accumbens associated 2, BEN and BTB (POZ) domain containing	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1319560	Nacc2	nucleus accumbens associated 2, BEN and BTB (POZ) domain containing	gene	MP:0013406	abnormal epidermal immune compartment		IEA		N	RGD:5509061	20201231	MGI			
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537792
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150596
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:24656820
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0003605	fused kidneys		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150596
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150596
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0010980	ectopic ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0010981	abnormal branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0011486	ectopic ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0011760	abnormal ureteric bud tip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0011761	abnormal ureteric bud trunk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319562	Spry1	sprouty RTK signaling antagonist 1	gene	MP:0011797	blind ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:15691764
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20150430	MGI			
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20150430	MGI			
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0010228	decreased transitional stage T3 B cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319567	Ell2	elongation factor for RNA polymerase II 2	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20160929	MGI			PMID:25238757
1319572	Mmel1	membrane metalloendopeptidase like 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121861
1319572	Mmel1	membrane metalloendopeptidase like 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121861
1319572	Mmel1	membrane metalloendopeptidase like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121861
1319579	Cers4	ceramide synthase 4	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0009004	progressive hair loss		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20151015	MGI			PMID:24738593
1319579	Cers4	ceramide synthase 4	gene	MP:0030571	dilated piliary canal		IAGP		N	RGD:5509061	20180524	MGI			PMID:24738593
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15946934
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15946934
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201022	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15946934
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981116
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:15946934
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15946934
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15946934
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0003883	enlarged stomach		IEA		N	RGD:5509061	20210520	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0005238	increased brain size		IEA		N	RGD:5509061	20210520	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15946934
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981116
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15946934
1319581	Spred2	sprouty-related EVH1 domain containing 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730163
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11528400
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730163
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730163
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730132
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730163
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003010	decreased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730132
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730163
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0004567	decreased myocardial fiber number		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730163
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20170831	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190221	MGI			
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190221	MGI			
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0008082	increased single-positive T cell number		IEA		N	RGD:5509061	20190221	MGI			
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20190221	MGI			
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20260813	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354690
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11528400
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730132
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21730163
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361844
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962274
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:12101245
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616333
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19573810
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17526734
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:21730163
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:17533180
1319585	Mdm4	MDM4 regulator of p53	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:23770245
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1319588	Ufl1	UFM1 specific ligase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170314	MGI			PMID:25952549
1319590	Irx4	Iroquois homeobox 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238910
1319590	Irx4	Iroquois homeobox 4	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238910
1319590	Irx4	Iroquois homeobox 4	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238910
1319590	Irx4	Iroquois homeobox 4	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238910
1319590	Irx4	Iroquois homeobox 4	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238910
1319590	Irx4	Iroquois homeobox 4	gene	MP:0008727	increased heart right atrium size		IAGP		N	RGD:5509061	20231221	MGI			PMID:11238910
1319590	Irx4	Iroquois homeobox 4	gene	MP:0011917	increased heart right atrium weight		IAGP		N	RGD:5509061	20231221	MGI			PMID:11238910
1319591	Tmem94	transmembrane protein 94	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1319591	Tmem94	transmembrane protein 94	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1319591	Tmem94	transmembrane protein 94	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0008443	absent subplate		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0010489	abnormal heart atrium auricular region morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0030245	round head		IAGP		N	RGD:5509061	20190919	MGI			PMID:30526868
1319591	Tmem94	transmembrane protein 94	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231102	MGI			PMID:30526868
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20230601	MGI			
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230601	MGI			
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343139
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343139
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20250508	MGI			
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343139
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343139
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343139
1319592	Nxnl2	nucleoredoxin-like 2	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343139
1319600	Slc2a6	solute carrier family 2 (facilitated glucose transporter), member 6	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:30431159
1319600	Slc2a6	solute carrier family 2 (facilitated glucose transporter), member 6	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20210617	MGI			PMID:30431159
1319600	Slc2a6	solute carrier family 2 (facilitated glucose transporter), member 6	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20210617	MGI			PMID:30431159
1319600	Slc2a6	solute carrier family 2 (facilitated glucose transporter), member 6	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20191010	MGI			PMID:29664675
1319600	Slc2a6	solute carrier family 2 (facilitated glucose transporter), member 6	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20191010	MGI			PMID:29664675
1319602	Adcy1	adenylate cyclase 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1319602	Adcy1	adenylate cyclase 1	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524897
1319602	Adcy1	adenylate cyclase 1	gene	MP:0000861	disorganized barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8596955
1319602	Adcy1	adenylate cyclase 1	gene	MP:0000862	absent barrels in primary somatosensory cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524897
1319602	Adcy1	adenylate cyclase 1	gene	MP:0000862	absent barrels in primary somatosensory cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8596955
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20200402	MGI			
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20200402	MGI			
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:7816821
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482244
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482244
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524897
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525048
1319602	Adcy1	adenylate cyclase 1	gene	MP:0001908	abnormal somatosensory cortex physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8596955
1319602	Adcy1	adenylate cyclase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200402	MGI			
1319602	Adcy1	adenylate cyclase 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524897
1319602	Adcy1	adenylate cyclase 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1319602	Adcy1	adenylate cyclase 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525048
1319602	Adcy1	adenylate cyclase 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:7816821
1319602	Adcy1	adenylate cyclase 1	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524897
1319602	Adcy1	adenylate cyclase 1	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482244
1319602	Adcy1	adenylate cyclase 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20230720	MGI			
1319602	Adcy1	adenylate cyclase 1	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441059
1319602	Adcy1	adenylate cyclase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7816821
1319602	Adcy1	adenylate cyclase 1	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441059
1319602	Adcy1	adenylate cyclase 1	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1319602	Adcy1	adenylate cyclase 1	gene	MP:0014372	decreased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240328	MGI			PMID:18524897
1319605	Top3a	topoisomerase (DNA) III alpha	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1319605	Top3a	topoisomerase (DNA) III alpha	gene	MP:0004966	abnormal inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9448276
1319605	Top3a	topoisomerase (DNA) III alpha	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20201022	MGI			
1319605	Top3a	topoisomerase (DNA) III alpha	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9448276
1319605	Top3a	topoisomerase (DNA) III alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319605	Top3a	topoisomerase (DNA) III alpha	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1319609	Ltk	leukocyte tyrosine kinase	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1319609	Ltk	leukocyte tyrosine kinase	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1319609	Ltk	leukocyte tyrosine kinase	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20230601	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293698
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293698
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837033
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837032
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000555	absent carpal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163358
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20141003	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20141003	MGI			PMID:21402791
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20161117	MGI			PMID:27524797
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20170706	MGI			PMID:28356706
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27524797
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20161117	MGI			PMID:27524797
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002183	gliosis		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263894
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19154719
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837033
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27524797
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:28356706
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837033
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003074	absent metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003727	abnormal retina layer morphology		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293698
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003800	monodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837032
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293698
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21602802
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20170706	MGI			PMID:28356706
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293698
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293698
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16293698
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005201	abnormal retina pigment epithelium morphology		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005322	abnormal serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21602802
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:28356706
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008067	retina ganglion cell degeneration		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008156	decreased diameter of tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008274	failure of bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008450	retina photoreceptor degeneration		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008512	disorganized retina inner nuclear layer		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008513	thin retina inner plexiform layer		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008515	thin retina outer nuclear layer		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008516	disorganized retina outer nuclear layer		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008519	thin retina outer plexiform layer		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0008520	disorganized retina outer plexiform layer		IEA		N	RGD:5509061	20111116	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0009869	abnormal descending aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837032
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20180927	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180927	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27524797
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20170706	MGI			PMID:28356706
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010961	increased compact bone mass		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010962	decreased compact bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0010962	decreased compact bone mass		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956231
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837032
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20161117	MGI			PMID:27524797
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0012035	abnormal b-wave shape		IAGP		N	RGD:5509061	20161117	MGI			PMID:27524797
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0012139	increased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20170706	MGI			PMID:28356706
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20170706	MGI			PMID:28356706
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0013207	absent endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20170706	MGI			PMID:28356706
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0013639	decreased bone stiffness		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0013640	increased bone stiffness		IAGP		N	RGD:5509061	20150507	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0013925	abnormal vascular plexus formation		IAGP		N	RGD:5509061	20161117	MGI			PMID:27524797
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0014179	abnormal blood-retina barrier function		IAGP		N	RGD:5509061	20170706	MGI			PMID:28356706
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:15142971
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:15537447
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:16293698
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:17147489
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:16293698
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:24225945
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0021107	retina fold		IEA		N	RGD:5509061	20220331	MGI			
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0030281	thin parietal bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:12509515
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0030439	decreased osteoblast proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:19041748
1319618	Lrp5	low density lipoprotein receptor-related protein 5	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IEA		N	RGD:5509061	20240404	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20210128	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210826	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20190502	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151112	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20200402	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20211021	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210520	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0006241	abnormal placement of pupils		IEA		N	RGD:5509061	20210128	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0010571	shortened ST segment		IEA		N	RGD:5509061	20211021	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250424	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0011392	increased fetal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20150924	MGI			PMID:24425002
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0011392	increased fetal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1319621	Ppp2r5c	protein phosphatase 2, regulatory subunit B', gamma	gene	MP:0031611	decreased fetal cardiomyocyte number		IAGP		N	RGD:5509061	20240404	MGI			PMID:24425002
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20150402	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0000531	right pulmonary isomerism		IEA		N	RGD:5509061	20150402	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20150402	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20150402	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0004110	transposition of great arteries		IEA		N	RGD:5509061	20150402	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20141003	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0006123	tricuspid valve atresia		IEA		N	RGD:5509061	20141003	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20150402	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0010422	heart right ventricle hypoplasia		IEA		N	RGD:5509061	20150402	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0010808	right-sided stomach		IEA		N	RGD:5509061	20150402	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0011665	d-loop transposition of the great arteries		IEA		N	RGD:5509061	20141003	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20150402	MGI			
1319623	Mmp21	matrix metallopeptidase 21	gene	MP:0011668	double outlet right ventricle, Taussig bing type		IEA		N	RGD:5509061	20150402	MGI			
1319627	Ate1	arginyltransferase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1319627	Ate1	arginyltransferase 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1319627	Ate1	arginyltransferase 1	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20241121	MGI			
1319627	Ate1	arginyltransferase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19890395
1319627	Ate1	arginyltransferase 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19890395
1319627	Ate1	arginyltransferase 1	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20230601	MGI			
1319627	Ate1	arginyltransferase 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1319627	Ate1	arginyltransferase 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0010502	ventricle myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12098698
1319627	Ate1	arginyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1319627	Ate1	arginyltransferase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0011854	cerebral edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19915679
1319627	Ate1	arginyltransferase 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20240523	MGI			
1319627	Ate1	arginyltransferase 1	gene	MP:0014729	abnormal myocardial fiber myofibril maturation		IAGP		N	RGD:5509061	20250911	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:18948421
1319627	Ate1	arginyltransferase 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:19915679
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287858
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855341
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287858
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0003436	decreased susceptibility to induced arthritis		IEA		N	RGD:5509061	20111116	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IEA		N	RGD:5509061	20111116	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0005095	decreased T cell proliferation		IEA		N	RGD:5509061	20111116	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IEA		N	RGD:5509061	20111116	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IEA		N	RGD:5509061	20111116	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0008561	decreased tumor necrosis factor secretion		IEA		N	RGD:5509061	20111116	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0008567	decreased interferon-gamma secretion		IEA		N	RGD:5509061	20111116	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0008660	increased interleukin-10 secretion		IEA		N	RGD:5509061	20111116	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20150702	MGI			PMID:16287858
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IEA		N	RGD:5509061	20111116	MGI			
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20240118	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:21768366
1319635	Mapk11	mitogen-activated protein kinase 11	gene	MP:0031526	thin right ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:21768366
1319636	Tmem192	transmembrane protein 192	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:28504966
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0004181	abnormal carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0006049	semilunar valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0009389	abnormal extracutaneous pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0010589	common truncal valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548583
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20240118	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688556
1319639	Sema3c	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C	gene	MP:0031517	interrupted aortic arch, type c		IAGP		N	RGD:5509061	20240118	MGI			PMID:11688556
1319641	Ropn1l	ropporin 1-like	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20160421	MGI			
1319641	Ropn1l	ropporin 1-like	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201231	MGI			
1319641	Ropn1l	ropporin 1-like	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021175
1319641	Ropn1l	ropporin 1-like	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201231	MGI			
1319641	Ropn1l	ropporin 1-like	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20160421	MGI			
1319641	Ropn1l	ropporin 1-like	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1319641	Ropn1l	ropporin 1-like	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021175
1319641	Ropn1l	ropporin 1-like	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:22021175
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894265
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636294
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092811
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23027924
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980208
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092811
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980208
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894265
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002440	abnormal memory B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23027924
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092811
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22962683
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23027924
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636294
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636294
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23027924
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980208
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008179	absent germinal center B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:23027924
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636294
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008194	abnormal memory B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23027924
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008523	absent lymph node germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9171827
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980208
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980208
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220623	MGI			PMID:11092811
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0010187	decreased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636294
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0010187	decreased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23027924
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0010187	decreased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0010187	decreased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980208
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0010188	abnormal T follicular helper cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980208
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0010674	increased activation-induced B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636294
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10533607
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23455674
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:11092811
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0020583	decreased ceramide level		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0020867	increased lipogenesis		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20190509	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0030973	impaired gluconeogenesis		IAGP		N	RGD:5509061	20200102	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:30566857
1319643	Bcl6	B cell leukemia/lymphoma 6	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:30566857
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24185898
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0000608	dissociated hepatocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20210128	MGI			
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20220519	MGI			
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210128	MGI			
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0003904	decreased cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0010889	small alveolar lamellar bodies		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17015619
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:20716775
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200116	MGI			PMID:26075877
1319645	Rb1cc1	RB1-inducible coiled-coil 1	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:26075877
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19364276
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201022	MGI			
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20201022	MGI			
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001095	enlarged trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15492043
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19364276
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201022	MGI			
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19364276
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19364276
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201022	MGI			
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19364276
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20160421	MGI			
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0006102	decreased tegmentum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19364276
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537918
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159989
1319650	Hipk2	homeodomain interacting protein kinase 2	gene	MP:0020543	decreased substantia nigra size		IAGP		N	RGD:5509061	20180301	MGI			PMID:17159989
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20823251
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20823251
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20823251
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20823251
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0005068	abnormal NK cell morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:30383838
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20220428	MGI			PMID:30383838
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20823251
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20220428	MGI			PMID:30383838
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20823251
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20220428	MGI			PMID:30383838
1319651	Urah	urate (5-hydroxyiso-) hydrolase	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20220428	MGI			PMID:30383838
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0000798	abnormal frontal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909942
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0001934	increased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909942
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10523632
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909942
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909942
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909942
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0003749	down-turned corners of mouth		IAGP		N	RGD:5509061	20171019	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909942
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909942
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909942
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909942
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0009432	increased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867340
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11977979
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11021537
1319653	Fes	Fes proto-oncogene, tyrosine kinase	gene	MP:0030192	downturned snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:11977979
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23319563
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805139
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805139
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805139
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17596337
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0003369	abnormal circulating estrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805139
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23319563
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23319563
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23319563
1319656	Mrc1	mannose receptor, C type 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805139
1319658	Ctsw	cathepsin W	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15087452
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20210128	MGI			
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210128	MGI			
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20210128	MGI			
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20260402	MGI			
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1319661	Rxylt1	ribitol xylosyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319663	Lrfn5	leucine rich repeat and fibronectin type III domain containing 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1319663	Lrfn5	leucine rich repeat and fibronectin type III domain containing 5	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1319663	Lrfn5	leucine rich repeat and fibronectin type III domain containing 5	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1319663	Lrfn5	leucine rich repeat and fibronectin type III domain containing 5	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20240523	MGI			
1319663	Lrfn5	leucine rich repeat and fibronectin type III domain containing 5	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1319663	Lrfn5	leucine rich repeat and fibronectin type III domain containing 5	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20240523	MGI			
1319666	Unc119b	unc-119 lipid binding chaperone B	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20231207	MGI			
1319667	Rgs7bp	regulator of G-protein signalling 7 binding protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18842904
1319669	Col8a1	collagen, type VIII, alpha 1	gene	MP:0003092	decreased cornea stroma thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1319669	Col8a1	collagen, type VIII, alpha 1	gene	MP:0004284	abnormal Descemet membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1319669	Col8a1	collagen, type VIII, alpha 1	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1319669	Col8a1	collagen, type VIII, alpha 1	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1319669	Col8a1	collagen, type VIII, alpha 1	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1319669	Col8a1	collagen, type VIII, alpha 1	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16051690
1319669	Col8a1	collagen, type VIII, alpha 1	gene	MP:0031177	decreased Descemet membrane thickness		IAGP		N	RGD:5509061	20201119	MGI			PMID:16051690
1319669	Col8a1	collagen, type VIII, alpha 1	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:16051690
1319672	Cdca7	cell division cycle associated 7	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20240404	MGI			PMID:38335290
1319674	F11	coagulation factor XI	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0002343	abnormal lymph node cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533887
1319674	F11	coagulation factor XI	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533887
1319674	F11	coagulation factor XI	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20151203	MGI			PMID:16009717
1319674	F11	coagulation factor XI	gene	MP:0010178	increased number of Howell-Jolly bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20141003	MGI			PMID:9518045
1319674	F11	coagulation factor XI	gene	MP:0031051	lymph node hemorrhage		IAGP		N	RGD:5509061	20200618	MGI			PMID:11159184
1319674	F11	coagulation factor XI	gene	MP:0031126	gangrene		IAGP		N	RGD:5509061	20200917	MGI			PMID:11159184
1319682	Med30	mediator complex subunit 30	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0000278	abnormal myocardial fiber morphology		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0001577	anemia		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0003135	increased erythroid progenitor cell number		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0004090	abnormal sarcomere morphology		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0004091	abnormal Z line morphology		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0005150	cachexia		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0005330	cardiomyopathy		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0006035	abnormal mitochondrial morphology		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0006036	abnormal mitochondrial physiology		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0006085	myocardium necrosis		IEA		N	RGD:5509061	20141003	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0010334	pleural effusion		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22106289
1319682	Med30	mediator complex subunit 30	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0014788	decreased protein level		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0030567	abnormal I band morphology		IEA		N	RGD:5509061	20180531	MGI			
1319682	Med30	mediator complex subunit 30	gene	MP:0031525	thin left ventricle myocardium compact layer		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0031526	thin right ventricle myocardium compact layer		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319682	Med30	mediator complex subunit 30	gene	MP:0031645	increased myocardial fiber apoptosis		IAGP		N	RGD:5509061	20260326	MGI			PMID:34506481
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20170601	MGI			PMID:26774178
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20170601	MGI			PMID:26774178
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20170601	MGI			PMID:26774178
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20241121	MGI			
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20241121	MGI			
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20170601	MGI			PMID:26774178
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20170601	MGI			PMID:26774178
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20241121	MGI			
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319684	Tm6sf2	transmembrane 6 superfamily member 2	gene	MP:0010332	abnormal circulating apolipoprotein level		IAGP		N	RGD:5509061	20170302	MGI			PMID:27013658
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751370
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22075698
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751370
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751370
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22075698
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751370
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0003454	erythroderma		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20190530	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20190530	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005078	abnormal cytotoxic T cell physiology		IEA		N	RGD:5509061	20111116	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20190606	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751370
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751370
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751370
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008169	increased B-1b cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008176	abnormal germinal center B cell morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008213	absent immature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818157
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867037
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12867038
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008567	decreased interferon-gamma secretion		IEA		N	RGD:5509061	20111116	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751370
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008627	decreased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751370
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008686	abnormal interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818158
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008688	decreased interleukin-2 secretion		IEA		N	RGD:5509061	20111116	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19260764
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0009925	increased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0010228	decreased transitional stage T3 B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0010228	decreased transitional stage T3 B cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:41307991
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0010766	abnormal NK cell physiology		IEA		N	RGD:5509061	20111116	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0010842	decreased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190530	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20190404	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0013763	increased T-helper cell number		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20230119	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20190606	MGI			
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20210128	MGI			PMID:31784498
1319686	Card11	caspase recruitment domain family, member 11	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20201231	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000829	dilated fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387364
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0003657	abnormal erythrocyte osmotic lysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20190502	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20260402	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20200402	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589692
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20190502	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9070925
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0011952	decreased cardiac stroke volume		IEA		N	RGD:5509061	20220519	MGI			
1319691	Nek1	NIMA (never in mitosis gene a)-related expressed kinase 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:15515002
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15515002
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15515002
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15515002
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20971813
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15515002
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20210304	MGI			PMID:30853435
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15515002
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20210304	MGI			PMID:30853435
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20210304	MGI			PMID:30853435
1319693	Rec8	REC8 meiotic recombination protein	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15935783
1319695	Scap	SREBF chaperone	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1319695	Scap	SREBF chaperone	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358865
1319695	Scap	SREBF chaperone	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358865
1319695	Scap	SREBF chaperone	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358865
1319695	Scap	SREBF chaperone	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358865
1319695	Scap	SREBF chaperone	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358865
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20200402	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060883
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060883
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060883
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20201022	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20210520	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200402	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20201022	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060883
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060883
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060883
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20250508	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20181011	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20200402	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20200402	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005425	increased macrophage cell number		IEA		N	RGD:5509061	20181011	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008126	increased dendritic cell number		IEA		N	RGD:5509061	20181011	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008167	increased B-1a cell number		IEA		N	RGD:5509061	20181011	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20181011	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20181011	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20181011	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008690	increased interleukin-23 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060883
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20201022	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20200402	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785118
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060883
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011580
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20210128	MGI			
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:19060883
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:21606507
1319698	Tnip1	TNFAIP3 interacting protein 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20181227	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15613470
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17613256
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231123	MGI			PMID:20018673
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16462742
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16040801
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16040801
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15613470
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000690	absent spleen		IEA		N	RGD:5509061	20200402	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867090
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:18463241
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129368
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452165
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160204	MGI			PMID:22331912
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001280	loss of vibrissae		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20200116	MGI			PMID:18463241
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16462742
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15613470
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528307
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15613470
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:15613470
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528307
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16040801
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329371
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001863	blood vessel inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701646
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129368
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24209619
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:22331912
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160204	MGI			PMID:22331912
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16462742
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160218	MGI			PMID:25329700
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701646
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701646
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002827	abnormal renal corpuscle morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20180531	MGI			PMID:28337978
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20181129	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16040801
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003574	abnormal oviduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003574	abnormal oviduct morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:22331912
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:22331912
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003700	abnormal oviduct transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16040801
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:18463241
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003875	abnormal hair follicle regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360310
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15613470
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004458	absent alisphenoid bone		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004476	absent palatine bone		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004728	abnormal efferent ductules of testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701646
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004880	lung cyst		IAGP		N	RGD:5509061	20160324	MGI			PMID:25978641
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004882	enlarged lung		IAGP		N	RGD:5509061	20160324	MGI			PMID:25978641
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004899	absent temporal bone squamous part		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701646
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701646
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004941	abnormal regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20181011	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329371
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867090
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009718
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009718
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009718
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129368
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24209619
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20160204	MGI			PMID:22331912
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20160204	MGI			PMID:25815421
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009718
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009718
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22474261
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009718
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16462742
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231123	MGI			PMID:20018673
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006213	shallow orbits		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452165
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25978641
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009718
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0006428	ectopic Sertoli cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008018	increased facial tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20181011	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008094	absent memory B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008100	absent plasma cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329371
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329371
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329371
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329371
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008257	thin myometrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867090
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:18463241
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:18463241
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008755	abnormal immunoglobulin V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329371
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009004	progressive hair loss		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009071	short oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009089	short uterine horn		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009140	dilated efferent ductule of testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701646
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009235	small sperm head		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009236	pinhead sperm		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009242	thin sperm flagellum		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009377	ectopic manchette		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20200116	MGI			PMID:18463241
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009439	increased myeloid sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22179202
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009600	hypergranulosis		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19129368
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010241	abnormal aortic arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:24979267
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231123	MGI			PMID:20018673
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20231123	MGI			PMID:20018673
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22434867
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010964	increased compact bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0010976	small lung lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452165
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20160324	MGI			PMID:25978641
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16462742
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452165
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180531	MGI			PMID:28337978
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16575173
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17613256
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528307
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16040801
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20231123	MGI			PMID:20018673
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15613470
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098571
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16575173
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011142	abnormal lung-associated mesenchyme development		IAGP		N	RGD:5509061	20160324	MGI			PMID:25978641
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011147	increased mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20160324	MGI			PMID:25978641
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22701646
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011846	decreased kidney collecting duct number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20170824	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:18463241
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:18463241
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20180531	MGI			PMID:28337978
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20200827	MGI			PMID:31766249
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0013305	isosthenuria		IAGP		N	RGD:5509061	20160929	MGI			PMID:25799508
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20150312	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014194	increased epididymal epithelium cell proliferation		IAGP		N	RGD:5509061	20160526	MGI			PMID:22701646
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:16040801
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014445	abnormal spindle assembly in female meiosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:19129368
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014445	abnormal spindle assembly in female meiosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:24209619
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17613256
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17613256
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17613256
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:18591425
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0021217	abnormal palatal shelf bone ossification		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0030025	giant platelets		IAGP		N	RGD:5509061	20170803	MGI			PMID:20305640
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0030102	absent orbitosphenoid bone		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0030262	frontal bossing		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0030266	small vomer bone		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0030301	abnormal maxillary frontal process morphology		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0030315	small neurocranium		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0030575	decreased hair follicle cell proliferation		IAGP		N	RGD:5509061	20181129	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0030591	absent sperm fibrous sheath		IAGP		N	RGD:5509061	20220324	MGI			PMID:21949761
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0030920	small hair follicle bulb		IAGP		N	RGD:5509061	20181220	MGI			PMID:16682203
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0031147	abnormal ventricular thrombosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:18256189
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0031407	increased Sertoli cell proliferation		IAGP		N	RGD:5509061	20220630	MGI			PMID:19071104
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:18703631
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230316	MGI			PMID:23716939
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:18463241
1319700	Dicer1	dicer 1, ribonuclease type III	gene	MP:0031613	fetal cardiomyocyte disarray		IAGP		N	RGD:5509061	20240321	MGI			PMID:18256189
1319704	Rnf24	ring finger protein 24	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1319704	Rnf24	ring finger protein 24	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1319714	Hmcn2	hemicentin 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210429	MGI			PMID:32035013
1319714	Hmcn2	hemicentin 2	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20201022	MGI			
1319714	Hmcn2	hemicentin 2	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20221215	MGI			
1319714	Hmcn2	hemicentin 2	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20201022	MGI			
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319716	Cmtr2	cap methyltransferase 2	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20260813	MGI			PMID:42417195
1319720	Tbx20	T-box 20	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1319720	Tbx20	T-box 20	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1319720	Tbx20	T-box 20	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20210128	MGI			
1319720	Tbx20	T-box 20	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843407
1319720	Tbx20	T-box 20	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1319720	Tbx20	T-box 20	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1319720	Tbx20	T-box 20	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1319720	Tbx20	T-box 20	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20210826	MGI			
1319720	Tbx20	T-box 20	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20230601	MGI			
1319720	Tbx20	T-box 20	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20220519	MGI			
1319720	Tbx20	T-box 20	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210826	MGI			
1319720	Tbx20	T-box 20	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20210128	MGI			
1319720	Tbx20	T-box 20	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843407
1319720	Tbx20	T-box 20	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1319720	Tbx20	T-box 20	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210128	MGI			
1319720	Tbx20	T-box 20	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1319720	Tbx20	T-box 20	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843407
1319720	Tbx20	T-box 20	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20210128	MGI			
1319720	Tbx20	T-box 20	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20210128	MGI			
1319720	Tbx20	T-box 20	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20210128	MGI			
1319720	Tbx20	T-box 20	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20230601	MGI			
1319720	Tbx20	T-box 20	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20210128	MGI			
1319720	Tbx20	T-box 20	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0004063	dilated heart left atrium		IAGP		N	RGD:5509061	20231221	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843407
1319720	Tbx20	T-box 20	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1319720	Tbx20	T-box 20	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20201029	MGI			PMID:32035085
1319720	Tbx20	T-box 20	gene	MP:0009806	abnormal otic vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1319720	Tbx20	T-box 20	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20201029	MGI			PMID:32035085
1319720	Tbx20	T-box 20	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843407
1319720	Tbx20	T-box 20	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1319720	Tbx20	T-box 20	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319720	Tbx20	T-box 20	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:15843407
1319720	Tbx20	T-box 20	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:15901664
1319720	Tbx20	T-box 20	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1319720	Tbx20	T-box 20	gene	MP:0020516	abnormal visceral yolk sac mesenchyme morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231221	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:15843414
1319720	Tbx20	T-box 20	gene	MP:0031572	small atrioventricular valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:23824573
1319720	Tbx20	T-box 20	gene	MP:0031582	small semilunar valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:23824573
1319720	Tbx20	T-box 20	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15843414
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24271779
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141016	MGI			PMID:24271779
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24271779
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24271779
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141016	MGI			PMID:24271779
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20141016	MGI			PMID:24271779
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20180510	MGI			PMID:27496549
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0014388	decreased hepatocyte mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:27496549
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0014390	decreased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:27496549
1319722	Sucla2	succinate-Coenzyme A ligase, ADP-forming, beta subunit	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20190711	MGI			PMID:24271779
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753194
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753194
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20111116	MGI			
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753194
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753195
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753194
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753195
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753194
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0004230	abnormal embryonic erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753195
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IEA		N	RGD:5509061	20111116	MGI			
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0005096	erythroblastosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753194
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0008807	increased liver iron level		IEA		N	RGD:5509061	20111116	MGI			
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0008809	increased spleen iron level		IEA		N	RGD:5509061	20111116	MGI			
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0009395	increased nucleated erythrocyte cell number		IEA		N	RGD:5509061	20111116	MGI			
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0010375	increased kidney iron level		IEA		N	RGD:5509061	20111116	MGI			
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409822
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753194
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7753195
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260507	MGI			PMID:7753195
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:7753194
1319724	Klf1	Kruppel-like transcription factor 1 (erythroid)	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:19409822
1319726	Lamc3	laminin gamma 3	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
1319726	Lamc3	laminin gamma 3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1319726	Lamc3	laminin gamma 3	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
1319726	Lamc3	laminin gamma 3	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
1319726	Lamc3	laminin gamma 3	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
1319726	Lamc3	laminin gamma 3	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
1319726	Lamc3	laminin gamma 3	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17711601
1319726	Lamc3	laminin gamma 3	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1319727	Ift20	intraflagellar transport 20	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20141003	MGI			
1319727	Ift20	intraflagellar transport 20	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:21307337
1319727	Ift20	intraflagellar transport 20	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1319727	Ift20	intraflagellar transport 20	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:21307337
1319727	Ift20	intraflagellar transport 20	gene	MP:0008448	abnormal retina cone cell inner segment morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:21307337
1319727	Ift20	intraflagellar transport 20	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:21307337
1319727	Ift20	intraflagellar transport 20	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:21307337
1319727	Ift20	intraflagellar transport 20	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0011843	abnormal kidney collecting duct epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0020384	absent kidney epithelial cell primary cilium		IAGP		N	RGD:5509061	20161013	MGI			PMID:18981227
1319727	Ift20	intraflagellar transport 20	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220224	MGI			PMID:27682589
1319727	Ift20	intraflagellar transport 20	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:27682589
1319728	Cend1	cell cycle exit and neuronal differentiation 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153830
1319728	Cend1	cell cycle exit and neuronal differentiation 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153830
1319728	Cend1	cell cycle exit and neuronal differentiation 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153830
1319728	Cend1	cell cycle exit and neuronal differentiation 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153830
1319728	Cend1	cell cycle exit and neuronal differentiation 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153830
1319728	Cend1	cell cycle exit and neuronal differentiation 1	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153830
1319728	Cend1	cell cycle exit and neuronal differentiation 1	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153830
1319728	Cend1	cell cycle exit and neuronal differentiation 1	gene	MP:0010540	long stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153830
1319733	Gpr35	G protein-coupled receptor 35	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20210211	MGI			PMID:32755573
1319733	Gpr35	G protein-coupled receptor 35	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210211	MGI			PMID:32755573
1319733	Gpr35	G protein-coupled receptor 35	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210916	MGI			PMID:33990686
1319733	Gpr35	G protein-coupled receptor 35	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20210916	MGI			PMID:33990686
1319733	Gpr35	G protein-coupled receptor 35	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20210916	MGI			PMID:33990686
1319733	Gpr35	G protein-coupled receptor 35	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20210211	MGI			PMID:32755573
1319733	Gpr35	G protein-coupled receptor 35	gene	MP:0013299	decreased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20210916	MGI			PMID:33990686
1319733	Gpr35	G protein-coupled receptor 35	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20210211	MGI			PMID:32755573
1319735	Fbxo5	F-box protein 5	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230601	MGI			
1319735	Fbxo5	F-box protein 5	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809773
1319735	Fbxo5	F-box protein 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1319735	Fbxo5	F-box protein 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1319735	Fbxo5	F-box protein 5	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1319735	Fbxo5	F-box protein 5	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1319735	Fbxo5	F-box protein 5	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809773
1319735	Fbxo5	F-box protein 5	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1319735	Fbxo5	F-box protein 5	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809773
1319735	Fbxo5	F-box protein 5	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230601	MGI			
1319735	Fbxo5	F-box protein 5	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809773
1319735	Fbxo5	F-box protein 5	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809773
1319735	Fbxo5	F-box protein 5	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809773
1319735	Fbxo5	F-box protein 5	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809773
1319735	Fbxo5	F-box protein 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1319735	Fbxo5	F-box protein 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230601	MGI			
1319735	Fbxo5	F-box protein 5	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
1319737	Ndufs3	NADH:ubiquinone oxidoreductase core subunit S3	gene	MP:0001391	abnormal tail movements		IEA		N	RGD:5509061	20160804	MGI			
1319737	Ndufs3	NADH:ubiquinone oxidoreductase core subunit S3	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20141003	MGI			
1319737	Ndufs3	NADH:ubiquinone oxidoreductase core subunit S3	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
1319737	Ndufs3	NADH:ubiquinone oxidoreductase core subunit S3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1319737	Ndufs3	NADH:ubiquinone oxidoreductase core subunit S3	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20211021	MGI			
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20181227	MGI			
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20210826	MGI			
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534538
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534538
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534538
1319739	Ing4	inhibitor of growth family, member 4	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534538
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20201022	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0003439	abnormal glycerol level		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20200402	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0010869	decreased bone trabecula number		IEA		N	RGD:5509061	20211021	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0012220	abnormal ether lipid level		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0013630	increased bone trabecular spacing		IEA		N	RGD:5509061	20211021	MGI			
1319744	Acbd5	acyl-Coenzyme A binding domain containing 5	gene	MP:0014010	abnormal peroxisome morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:33244184
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20240425	MGI			PMID:37532519
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20240425	MGI			PMID:37532519
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20240425	MGI			PMID:37532519
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20240425	MGI			PMID:37532519
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20240425	MGI			PMID:37532519
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20240425	MGI			PMID:37532519
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0010827	small lung saccule		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20231019	MGI			PMID:37553261
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240425	MGI			PMID:37532519
1319747	Zswim8	zinc finger SWIM-type containing 8	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231102	MGI			PMID:37553261
1319754	Gpr137	G protein-coupled receptor 137	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1319756	Kctd12	potassium channel tetramerisation domain containing 12	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20160421	MGI			PMID:25689571
1319756	Kctd12	potassium channel tetramerisation domain containing 12	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20160421	MGI			PMID:25689571
1319756	Kctd12	potassium channel tetramerisation domain containing 12	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20160421	MGI			PMID:25689571
1319756	Kctd12	potassium channel tetramerisation domain containing 12	gene	MP:0009455	enhanced cued conditioning behavior		IAGP		N	RGD:5509061	20160421	MGI			PMID:25689571
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0004974	decreased regulatory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20181227	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0005478	decreased circulating thyroxine level		IEA		N	RGD:5509061	20211021	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20181227	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20181227	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0011338	abnormal mesangial matrix morphology		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0011425	abnormal kidney interstitium morphology		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20181227	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0012767	increased KLRG1-positive NK cell number		IEA		N	RGD:5509061	20181227	MGI			
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319761	Ncf2	neutrophil cytosolic factor 2	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180726	MGI			PMID:28471497
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8197187
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8197187
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0002898	absent cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8197187
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0002999	abnormal bone healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10595929
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15802199
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11680679
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8197187
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0004591	enlarged tectorial membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:15802199
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8197187
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15802199
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8197187
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15802199
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0014091	abnormal tectorial membrane striated-sheet matrix morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:15802199
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0014100	increased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:8197187
1319762	Col9a1	collagen, type IX, alpha 1	gene	MP:0030837	abnormal knee joint morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:8197187
1319764	Dsc2	desmocollin 2	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20170504	MGI			
1319764	Dsc2	desmocollin 2	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20170504	MGI			
1319764	Dsc2	desmocollin 2	gene	MP:0001625	cardiac hypertrophy		IEA		N	RGD:5509061	20210429	MGI			
1319764	Dsc2	desmocollin 2	gene	MP:0002625	heart left ventricle hypertrophy		IEA		N	RGD:5509061	20210429	MGI			
1319764	Dsc2	desmocollin 2	gene	MP:0003141	cardiac fibrosis		IEA		N	RGD:5509061	20210429	MGI			
1319764	Dsc2	desmocollin 2	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20170504	MGI			
1319764	Dsc2	desmocollin 2	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20170504	MGI			
1319764	Dsc2	desmocollin 2	gene	MP:0006042	increased apoptosis		IEA		N	RGD:5509061	20210429	MGI			
1319764	Dsc2	desmocollin 2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IEA		N	RGD:5509061	20240704	MGI			
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727838
1319765	Tubb2b	tubulin, beta 2B class IIB	gene	MP:0012448	abnormal primary motor cortex morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1319768	Gsg1l	GSG1-like	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200514	MGI			
1319768	Gsg1l	GSG1-like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1319768	Gsg1l	GSG1-like	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1319768	Gsg1l	GSG1-like	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319768	Gsg1l	GSG1-like	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319768	Gsg1l	GSG1-like	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319768	Gsg1l	GSG1-like	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319768	Gsg1l	GSG1-like	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319768	Gsg1l	GSG1-like	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319768	Gsg1l	GSG1-like	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319768	Gsg1l	GSG1-like	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1319768	Gsg1l	GSG1-like	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1319768	Gsg1l	GSG1-like	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319768	Gsg1l	GSG1-like	gene	MP:0011272	short excitatory postsynaptic current rise time		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319768	Gsg1l	GSG1-like	gene	MP:0011274	short excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20210225	MGI			PMID:32697982
1319771	Adgrb2	adhesion G protein-coupled receptor B2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20170105	MGI			
1319771	Adgrb2	adhesion G protein-coupled receptor B2	gene	MP:0003063	increased coping response		IEA		N	RGD:5509061	20111116	MGI			
1319775	Cyp2u1	cytochrome P450, family 2, subfamily u, polypeptide 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201231	MGI			
1319775	Cyp2u1	cytochrome P450, family 2, subfamily u, polypeptide 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1319775	Cyp2u1	cytochrome P450, family 2, subfamily u, polypeptide 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319778	Nhp2	NHP2 ribonucleoprotein	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20211021	MGI			
1319778	Nhp2	NHP2 ribonucleoprotein	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20150108	MGI			
1319778	Nhp2	NHP2 ribonucleoprotein	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1319778	Nhp2	NHP2 ribonucleoprotein	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
1319778	Nhp2	NHP2 ribonucleoprotein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1319780	Ndufs8	NADH:ubiquinone oxidoreductase core subunit S8	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:23546880
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:23546880
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23546880
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260493
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260493
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22143887
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17085580
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001665	chronic diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17085580
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22143887
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0004972	abnormal regulatory T cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0004975	absent regulatory T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857737
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22143887
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005415	intrahepatic cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857737
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857737
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940043
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008350	increased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008399	abnormal alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:23546880
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0008895	abnormal intraepithelial T cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16857737
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0009623	enlarged inguinal lymph nodes		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0009631	enlarged axillary lymph nodes		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23546880
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23546880
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23546880
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23546880
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011009	increased circulating glutamate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478530
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23546880
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22348103
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260493
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17085580
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0011705	absent fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186825
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556914
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1319783	Map3k7	mitogen-activated protein kinase kinase kinase 7	gene	MP:0014201	abnormal intestinal epithelium physiology		IAGP		N	RGD:5509061	20170223	MGI			PMID:26132627
1319786	Lsm12	LSM12 homolog	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1319786	Lsm12	LSM12 homolog	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1319786	Lsm12	LSM12 homolog	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116426
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940229
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000151	absent ribs		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20230601	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15637299
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20230601	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:923728
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20221201	MGI			PMID:24689077
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11401449
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:24203697
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4230658
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20111116	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4230658
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:923728
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4230658
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:923728
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1138408
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1138408
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14512015
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11401449
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940229
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359061
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17566405
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20150924	MGI			PMID:25218921
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001391	abnormal tail movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11401449
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20220519	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20150924	MGI			PMID:25218921
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17566405
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359061
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20111116	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17566405
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002200	abnormal brain ventricular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:923728
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8088438
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940229
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25218921
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20141003	MGI			PMID:4230658
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:5955164
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002758	long tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11401449
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11707073
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359061
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:24203697
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11707073
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:15229603
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966784
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20704721
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:24203697
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20221201	MGI			PMID:36123354
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003126	abnormal external female genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11401449
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003384	abnormal ventral body wall morphology		IEA		N	RGD:5509061	20111229	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003540	imperforate hymen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18604206
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8088438
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4477997
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706528
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003936	abnormal reproductive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003938	abnormal ear development		IEA		N	RGD:5509061	20111116	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003942	abnormal urinary system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4230658
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004159	double aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359061
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359061
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11401449
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359061
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004302	abnormal Deiters cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004391	abnormal respiratory conducting tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25218921
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004406	abnormal cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940229
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004407	increased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116426
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004407	increased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116426
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940229
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:24203697
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116426
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20160128	MGI			PMID:24135232
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0005034	abnormal anus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0005222	abnormal somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0005222	abnormal somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0006014	dilated endolymphatic sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0006026	dilated terminal bronchiole tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11401449
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0006286	inner ear hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0006286	inner ear hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0006394	abnormal vertebral epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008149	abnormal costovertebral joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008307	short scala media		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:4230658
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:923728
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:923728
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11401449
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11707073
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20704721
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:4477997
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8088438
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9545534
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008832	hemivertebra		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008833	caudal hemivertebra		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0008933	abnormal motile primary cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0009199	abnormal external male genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19701191
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359061
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17566405
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0009929	meningomyelocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:17566405
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940229
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010466	vascular ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010488	abnormal left subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010589	common truncal valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010744	abnormal cervical flexure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11440971
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010866	abnormal prenatal body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010975	abnormal lung lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0010976	small lung lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011032	impaired branching involved in terminal bronchiole morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966784
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011089	perinatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16170314
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966784
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011172	abnormal otic pit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6650116
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22363783
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20230601	MGI			
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:13435227
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986237
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0012027	abnormal embryonic cilium location or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0012027	abnormal embryonic cilium location or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0012304	short umbilical cord		IAGP		N	RGD:5509061	20141003	MGI			PMID:14039372
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11401449
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359061
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0015003	decreased embryo length		IAGP		N	RGD:5509061	20260611	MGI			PMID:23406901
1319788	Vangl2	VANGL planar cell polarity 2	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20221201	MGI			PMID:24689077
1319791	Bicd1	BICD cargo adaptor 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210805	MGI			
1319791	Bicd1	BICD cargo adaptor 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210805	MGI			
1319791	Bicd1	BICD cargo adaptor 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1319791	Bicd1	BICD cargo adaptor 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210805	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0001800	abnormal humoral immune response		IEA		N	RGD:5509061	20141003	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357629
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357629
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002459	abnormal B cell physiology		IEA		N	RGD:5509061	20141003	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14638845
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20181004	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IEA		N	RGD:5509061	20180927	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20180927	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20181004	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181004	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181004	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20181004	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008343	abnormal gamma-delta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008464	absent peripheral lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697836
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705172
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20181004	MGI			
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150326	MGI			PMID:21441458
1319796	Ltbr	lymphotoxin B receptor	gene	MP:0020174	abnormal IgG level		IEA		N	RGD:5509061	20180215	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220519	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217959
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963592
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217959
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963592
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20160804	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15256493
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217959
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21467199
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15256493
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963592
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100620
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20160804	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160421	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0003673	abnormal inguinal canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217959
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963592
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20963592
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0005149	abnormal gubernaculum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217959
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217959
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0005573	increased pulmonary respiratory rate		IEA		N	RGD:5509061	20220811	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160421	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20160421	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21467199
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0009213	absent male inguinal canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217959
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0009251	enlarged endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:21467199
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20220519	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21467199
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20201022	MGI			
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20141218	MGI			PMID:21467199
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0013713	decreased nipple size		IAGP		N	RGD:5509061	20150402	MGI			PMID:15256493
1319798	Rxfp2	relaxin/insulin-like family peptide receptor 2	gene	MP:0031287	bilateral cryptorchism		IAGP		N	RGD:5509061	20211014	MGI			PMID:12217959
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210520	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20230601	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210128	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20200514	MGI			
1319799	Ppp4r3b	protein phosphatase 4 regulatory subunit 3B	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1319801	Sec24a	SEC24 homolog A, COPII coat complex component	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319801	Sec24a	SEC24 homolog A, COPII coat complex component	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1319801	Sec24a	SEC24 homolog A, COPII coat complex component	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319801	Sec24a	SEC24 homolog A, COPII coat complex component	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1319801	Sec24a	SEC24 homolog A, COPII coat complex component	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1319801	Sec24a	SEC24 homolog A, COPII coat complex component	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1319801	Sec24a	SEC24 homolog A, COPII coat complex component	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319801	Sec24a	SEC24 homolog A, COPII coat complex component	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20160804	MGI			
1319801	Sec24a	SEC24 homolog A, COPII coat complex component	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0009474	thick epidermis stratum spinosum		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0009596	abnormal stratum corneum lipid matrix formation		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0009602	abnormal keratohyalin granule morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0009604	increased keratohyalin granule number		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0009607	decreased keratohyalin granule size		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0009608	abnormal epidermal lamellar body morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0011979	abnormal magnesium ion homeostasis		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0020116	increased sphingosine level		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0020117	decreased sphingosine level		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0020583	decreased ceramide level		IAGP		N	RGD:5509061	20180621	MGI			PMID:29174370
1319802	Nipal4	NIPA-like domain containing 4	gene	MP:0030605	abnormal corneocyte morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:29174370
1319803	Lrrc71	leucine rich repeat containing 71	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1319805	Lix1	limb and CNS expressed 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21846745
1319807	Stk38	serine/threonine kinase 38	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1319807	Stk38	serine/threonine kinase 38	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20190905	MGI			PMID:30135513
1319807	Stk38	serine/threonine kinase 38	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20181206	MGI			PMID:20551432
1319807	Stk38	serine/threonine kinase 38	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20160602	MGI			PMID:25981615
1319807	Stk38	serine/threonine kinase 38	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20181206	MGI			PMID:20551432
1319807	Stk38	serine/threonine kinase 38	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1319807	Stk38	serine/threonine kinase 38	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20181206	MGI			PMID:20551432
1319807	Stk38	serine/threonine kinase 38	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20181206	MGI			PMID:20551432
1319807	Stk38	serine/threonine kinase 38	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1319807	Stk38	serine/threonine kinase 38	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20160602	MGI			PMID:25981615
1319807	Stk38	serine/threonine kinase 38	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20190905	MGI			PMID:30135513
1319807	Stk38	serine/threonine kinase 38	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20190905	MGI			PMID:30135513
1319807	Stk38	serine/threonine kinase 38	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1319807	Stk38	serine/threonine kinase 38	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20190905	MGI			PMID:30135513
1319807	Stk38	serine/threonine kinase 38	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20160602	MGI			PMID:25981615
1319807	Stk38	serine/threonine kinase 38	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25981615
1319807	Stk38	serine/threonine kinase 38	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20160602	MGI			PMID:25981615
1319807	Stk38	serine/threonine kinase 38	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25981615
1319807	Stk38	serine/threonine kinase 38	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20181206	MGI			PMID:20551432
1319807	Stk38	serine/threonine kinase 38	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20181206	MGI			PMID:20551432
1319807	Stk38	serine/threonine kinase 38	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20160602	MGI			PMID:25981615
1319807	Stk38	serine/threonine kinase 38	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20160602	MGI			PMID:25981615
1319807	Stk38	serine/threonine kinase 38	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319807	Stk38	serine/threonine kinase 38	gene	MP:0011996	abnormal retina inner nuclear layer thickness		IAGP		N	RGD:5509061	20190905	MGI			PMID:30135513
1319807	Stk38	serine/threonine kinase 38	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1319807	Stk38	serine/threonine kinase 38	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:30135513
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20210520	MGI			
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210520	MGI			
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20221215	MGI			
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20210520	MGI			
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20210826	MGI			
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20220602	MGI			PMID:35182466
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220602	MGI			PMID:35182466
1319811	Glyr1	glyoxylate reductase 1 homolog (Arabidopsis)	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20220602	MGI			PMID:35182466
1319813	Rigi	RNA sensor RIG-I	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650396
1319813	Rigi	RNA sensor RIG-I	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650396
1319813	Rigi	RNA sensor RIG-I	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1319813	Rigi	RNA sensor RIG-I	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230601	MGI			
1319813	Rigi	RNA sensor RIG-I	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650396
1319813	Rigi	RNA sensor RIG-I	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893708
1319813	Rigi	RNA sensor RIG-I	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1319813	Rigi	RNA sensor RIG-I	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893708
1319813	Rigi	RNA sensor RIG-I	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1319813	Rigi	RNA sensor RIG-I	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039576
1319813	Rigi	RNA sensor RIG-I	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650396
1319813	Rigi	RNA sensor RIG-I	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1319813	Rigi	RNA sensor RIG-I	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650396
1319813	Rigi	RNA sensor RIG-I	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650396
1319813	Rigi	RNA sensor RIG-I	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893708
1319813	Rigi	RNA sensor RIG-I	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039576
1319813	Rigi	RNA sensor RIG-I	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893708
1319813	Rigi	RNA sensor RIG-I	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18650396
1319813	Rigi	RNA sensor RIG-I	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1319813	Rigi	RNA sensor RIG-I	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893708
1319813	Rigi	RNA sensor RIG-I	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893708
1319813	Rigi	RNA sensor RIG-I	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893708
1319813	Rigi	RNA sensor RIG-I	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893708
1319813	Rigi	RNA sensor RIG-I	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1319813	Rigi	RNA sensor RIG-I	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1319813	Rigi	RNA sensor RIG-I	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039576
1319813	Rigi	RNA sensor RIG-I	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16039576
1319813	Rigi	RNA sensor RIG-I	gene	MP:0031044	increased susceptibility to Flaviviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:16625202
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000537	abnormal urethra morphology		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000823	abnormal lateral ventricle morphology		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0000961	abnormal dorsal root ganglion morphology		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001634	internal hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20200402	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20200402	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0002947	increased hemangioma incidence		IEA		N	RGD:5509061	20210930	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20200402	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0005655	increased aggression		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0008347	decreased gamma-delta T cell number		IEA		N	RGD:5509061	20170105	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0009493	abnormal cystic duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0012450	decreased primary motor cortex size		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0012466	decreased hippocampal fimbria size		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0012467	increased striatum size		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0012474	decreased cingulate cortex size		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0012768	decreased KLRG1-positive NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013022	increased Ly6C high monocyte number		IEA		N	RGD:5509061	20201022	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013025	increased Ly6C low monocyte number		IEA		N	RGD:5509061	20200402	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013648	increased CD11b-high dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013652	decreased CD11b-low dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0020083	decreased hippocampus volume		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0020396	abnormal social recognition		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0020543	decreased substantia nigra size		IAGP		N	RGD:5509061	20210708	MGI			PMID:32877400
1319814	Trappc9	trafficking protein particle complex 9	gene	MP:0030003	hippocampus atrophy		IAGP		N	RGD:5509061	20210617	MGI			PMID:33208359
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20180215	MGI			PMID:10675334
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676787
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676787
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675334
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676787
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675334
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675334
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0003843	abnormal sagittal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676787
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085687
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0008958	abnormal trophoblast glycogen cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675334
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11472836
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0010128	hypovolemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675334
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0011525	abnormal placenta intervillous maternal lacunae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0012099	decreased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0012109	decreased trophoblast glycogen cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:17584888
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0015010	delayed onset of definitive erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:12676787
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0030542	abnormal dentin development		IAGP		N	RGD:5509061	20180215	MGI			PMID:10675334
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0030544	abnormal enamel development		IAGP		N	RGD:5509061	20180215	MGI			PMID:10675334
1319819	Sp3	trans-acting transcription factor 3	gene	MP:0030989	decreased spongiotrophoblast cell number		IAGP		N	RGD:5509061	20191219	MGI			PMID:17584888
1319821	Exo1	exonuclease 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1319821	Exo1	exonuclease 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0008966	abnormal chiasmata formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0008967	absent chiasmata formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0009564	abnormal meiotic configurations		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0009797	abnormal mismatch repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0010094	abnormal chromosome stability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:12629043
1319821	Exo1	exonuclease 1	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:23754438
1319821	Exo1	exonuclease 1	gene	MP:0014766	impaired mismatch repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:12629043
1319824	Trem1	triggering receptor expressed on myeloid cells 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719066
1319824	Trem1	triggering receptor expressed on myeloid cells 1	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719066
1319824	Trem1	triggering receptor expressed on myeloid cells 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719066
1319824	Trem1	triggering receptor expressed on myeloid cells 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IEA		N	RGD:5509061	20201022	MGI			
1319824	Trem1	triggering receptor expressed on myeloid cells 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719066
1319824	Trem1	triggering receptor expressed on myeloid cells 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22719066
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591952
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591952
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0002742	enlarged submandibular lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591952
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591952
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591952
1319826	Top3b	topoisomerase (DNA) III beta	gene	MP:0009631	enlarged axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11331780
1319829	Ubxn1	UBX domain protein 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1319829	Ubxn1	UBX domain protein 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1319829	Ubxn1	UBX domain protein 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20240523	MGI			
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19204075
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220519	MGI			
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20220519	MGI			
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0011435	increased urine magnesium level		IEA		N	RGD:5509061	20250508	MGI			
1319830	Slc46a1	solute carrier family 46, member 1	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:19204075
1319834	Stard4	StAR related lipid transfer domain containing 4	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965609
1319834	Stard4	StAR related lipid transfer domain containing 4	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965609
1319834	Stard4	StAR related lipid transfer domain containing 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965609
1319834	Stard4	StAR related lipid transfer domain containing 4	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965609
1319834	Stard4	StAR related lipid transfer domain containing 4	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965609
1319834	Stard4	StAR related lipid transfer domain containing 4	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965609
1319836	Trim8	tripartite motif-containing 8	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1319836	Trim8	tripartite motif-containing 8	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20210128	MGI			
1319836	Trim8	tripartite motif-containing 8	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1319836	Trim8	tripartite motif-containing 8	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1319836	Trim8	tripartite motif-containing 8	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1319836	Trim8	tripartite motif-containing 8	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210429	MGI			PMID:27956576
1319836	Trim8	tripartite motif-containing 8	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210506	MGI			PMID:31360105
1319836	Trim8	tripartite motif-containing 8	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319836	Trim8	tripartite motif-containing 8	gene	MP:0011078	increased macrophage cytokine production		IAGP		N	RGD:5509061	20211202	MGI			PMID:28747347
1319838	Polr2b	polymerase (RNA) II (DNA directed) polypeptide B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1319838	Polr2b	polymerase (RNA) II (DNA directed) polypeptide B	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1319838	Polr2b	polymerase (RNA) II (DNA directed) polypeptide B	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1319838	Polr2b	polymerase (RNA) II (DNA directed) polypeptide B	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1319838	Polr2b	polymerase (RNA) II (DNA directed) polypeptide B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1319838	Polr2b	polymerase (RNA) II (DNA directed) polypeptide B	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20241010	MGI			
1319840	Bnipl	BCL2/adenovirus E1B 19kD interacting protein like	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
1319840	Bnipl	BCL2/adenovirus E1B 19kD interacting protein like	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20250508	MGI			
1319840	Bnipl	BCL2/adenovirus E1B 19kD interacting protein like	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20250508	MGI			
1319843	Ints6	integrator complex subunit 6	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20250508	MGI			
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0008823	abnormal interventricular septum membranous part morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0010498	abnormal interventricular septum muscular part morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20250508	MGI			
1319852	Bcl7a	B cell CLL/lymphoma 7A	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18064674
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20230119	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147379
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001015	small superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147379
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001017	abnormal stellate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147379
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147379
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20231207	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20231207	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147379
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18064674
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230119	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18064674
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18064674
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20231207	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003201	extremity edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:9815146
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20230119	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20231207	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147379
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9815146
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0004323	sternum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20230119	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20230119	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0005252	abnormal Meibomian gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147379
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20230119	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0008068	absent retina ganglion cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0008510	absent retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0008514	absent retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0009284	abnormal sympathetic neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147379
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20230119	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20231207	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010395	abnormal pharyngeal arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010417	subarterial ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010500	myocardium hypoplasia		IAGP		N	RGD:5509061	20240125	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010572	persistent right dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:9815146
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9815146
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010645	failure of conotruncal ridge closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010650	abnormal aorticopulmonary septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109771
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18064674
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477811
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8614465
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011261	abnormal limb mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0011262	abnormal pharyngeal arch mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:23649630
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:20596238
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0031553	abnormal semilunar valve development		IAGP		N	RGD:5509061	20240125	MGI			PMID:18064674
1319855	Sox4	SRY (sex determining region Y)-box 4	gene	MP:0031583	semilunar valve hypoplasia		IAGP		N	RGD:5509061	20240125	MGI			PMID:20596238
1319862	Rps6kl1	ribosomal protein S6 kinase-like 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220811	MGI			
1319862	Rps6kl1	ribosomal protein S6 kinase-like 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1319862	Rps6kl1	ribosomal protein S6 kinase-like 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20220811	MGI			
1319865	Srsf9	serine and arginine-rich splicing factor 9	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1319865	Srsf9	serine and arginine-rich splicing factor 9	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1319866	Alkbh5	alkB homolog 5, RNA demethylase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177736
1319866	Alkbh5	alkB homolog 5, RNA demethylase	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177736
1319866	Alkbh5	alkB homolog 5, RNA demethylase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177736
1319866	Alkbh5	alkB homolog 5, RNA demethylase	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177736
1319866	Alkbh5	alkB homolog 5, RNA demethylase	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177736
1319866	Alkbh5	alkB homolog 5, RNA demethylase	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177736
1319866	Alkbh5	alkB homolog 5, RNA demethylase	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177736
1319866	Alkbh5	alkB homolog 5, RNA demethylase	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23177736
1319868	Efnb2	ephrin B2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968134
1319868	Efnb2	ephrin B2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539827
1319868	Efnb2	ephrin B2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1319868	Efnb2	ephrin B2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630219
1319868	Efnb2	ephrin B2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630219
1319868	Efnb2	ephrin B2	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0000293	absent myocardial trabeculae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0000293	absent myocardial trabeculae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630219
1319868	Efnb2	ephrin B2	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0000424	retarded hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0000537	abnormal urethra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0000618	small salivary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14699416
1319868	Efnb2	ephrin B2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687262
1319868	Efnb2	ephrin B2	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:14699416
1319868	Efnb2	ephrin B2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687262
1319868	Efnb2	ephrin B2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539827
1319868	Efnb2	ephrin B2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0002349	abnormal afferent lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687262
1319868	Efnb2	ephrin B2	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539827
1319868	Efnb2	ephrin B2	gene	MP:0003125	abnormal septation of the cloaca		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0003128	splayed clitoris		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0003129	persistent cloaca		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0003130	anal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0003164	decreased posterior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0003166	decreased superior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630219
1319868	Efnb2	ephrin B2	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539827
1319868	Efnb2	ephrin B2	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687262
1319868	Efnb2	ephrin B2	gene	MP:0003660	chylothorax		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687262
1319868	Efnb2	ephrin B2	gene	MP:0003840	abnormal coronal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968134
1319868	Efnb2	ephrin B2	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630219
1319868	Efnb2	ephrin B2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630219
1319868	Efnb2	ephrin B2	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0004126	thin hypodermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630219
1319868	Efnb2	ephrin B2	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0004885	abnormal endolymph physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0004887	decreased endolymph production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0004922	abnormal common crus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0005187	abnormal penis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17336907
1319868	Efnb2	ephrin B2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17336907
1319868	Efnb2	ephrin B2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21847105
1319868	Efnb2	ephrin B2	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0006014	dilated endolymphatic sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0006344	small second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0006389	abnormal vestibular endolymph physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0006391	abnormal vestibular endolymph ionic homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0008066	small endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158005
1319868	Efnb2	ephrin B2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0010600	enlarged pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0010617	thick mitral valve cusps		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0010860	abnormal anterior commissure pars posterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687262
1319868	Efnb2	ephrin B2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571816
1319868	Efnb2	ephrin B2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223334
1319868	Efnb2	ephrin B2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539827
1319868	Efnb2	ephrin B2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968134
1319868	Efnb2	ephrin B2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9630219
1319868	Efnb2	ephrin B2	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880349
1319868	Efnb2	ephrin B2	gene	MP:0012493	absent pharyngeal arch arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163240
1319868	Efnb2	ephrin B2	gene	MP:0012755	decreased cranial neural crest cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0012761	increased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0013012	abnormal trunk neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17223098
1319868	Efnb2	ephrin B2	gene	MP:0014751	abnormal commissural neuron axon guidance		IAGP		N	RGD:5509061	20250904	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:21976681
1319868	Efnb2	ephrin B2	gene	MP:0031529	pulmonary valve hyperplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:15223333
1319868	Efnb2	ephrin B2	gene	MP:0031568	aortic valve hyperplasia		IAGP		N	RGD:5509061	20240125	MGI			PMID:15223333
1319870	Pigo	phosphatidylinositol glycan anchor biosynthesis, class O	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20211021	MGI			
1319870	Pigo	phosphatidylinositol glycan anchor biosynthesis, class O	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20211021	MGI			
1319870	Pigo	phosphatidylinositol glycan anchor biosynthesis, class O	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319870	Pigo	phosphatidylinositol glycan anchor biosynthesis, class O	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1319872	Dok1	docking protein 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1319872	Dok1	docking protein 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1319872	Dok1	docking protein 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1319872	Dok1	docking protein 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1319872	Dok1	docking protein 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1319872	Dok1	docking protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1319872	Dok1	docking protein 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640270
1319872	Dok1	docking protein 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1319872	Dok1	docking protein 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1319872	Dok1	docking protein 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1319872	Dok1	docking protein 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1319872	Dok1	docking protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1319872	Dok1	docking protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1319872	Dok1	docking protein 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1319872	Dok1	docking protein 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11489947
1319872	Dok1	docking protein 1	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1319872	Dok1	docking protein 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1319872	Dok1	docking protein 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0004202	pulmonary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1319872	Dok1	docking protein 1	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11489947
1319872	Dok1	docking protein 1	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640270
1319872	Dok1	docking protein 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1319872	Dok1	docking protein 1	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1319872	Dok1	docking protein 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1319872	Dok1	docking protein 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20160414	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20160414	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20160414	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1319872	Dok1	docking protein 1	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1319872	Dok1	docking protein 1	gene	MP:0010829	increased bronchioalveolar stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1319872	Dok1	docking protein 1	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1319872	Dok1	docking protein 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11489947
1319872	Dok1	docking protein 1	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:18204460
1319872	Dok1	docking protein 1	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:18204460
1319874	Celf3	CUGBP, Elav-like family member 3	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17393433
1319874	Celf3	CUGBP, Elav-like family member 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17393433
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0003125	abnormal septation of the cloaca		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0006130	pulmonary valve atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0011060	abnormal kinocilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0011707	impaired fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0011865	abnormal podocyte motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24302887
1319875	Wdpcp	WD repeat containing planar cell polarity effector	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:24302887
1319878	Itm2c	integral membrane protein 2C	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1319878	Itm2c	integral membrane protein 2C	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:30042348
1319878	Itm2c	integral membrane protein 2C	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1319878	Itm2c	integral membrane protein 2C	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20201022	MGI			
1319878	Itm2c	integral membrane protein 2C	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319879	Actbl2	actin, beta-like 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20241121	MGI			
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319883	Rab30	RAB30, member RAS oncogene family	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38796472
1319885	Reep6	receptor accessory protein 6	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:28475715
1319885	Reep6	receptor accessory protein 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201022	MGI			PMID:32101290
1319885	Reep6	receptor accessory protein 6	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20201022	MGI			PMID:32101290
1319885	Reep6	receptor accessory protein 6	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20201022	MGI			PMID:32101290
1319885	Reep6	receptor accessory protein 6	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27889058
1319885	Reep6	receptor accessory protein 6	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27889058
1319885	Reep6	receptor accessory protein 6	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27889058
1319885	Reep6	receptor accessory protein 6	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20201022	MGI			PMID:32101290
1319885	Reep6	receptor accessory protein 6	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20201022	MGI			PMID:32101290
1319885	Reep6	receptor accessory protein 6	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20180809	MGI			PMID:27889058
1319885	Reep6	receptor accessory protein 6	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20180809	MGI			PMID:28475715
1319885	Reep6	receptor accessory protein 6	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20180809	MGI			PMID:28475715
1319885	Reep6	receptor accessory protein 6	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20180809	MGI			PMID:27889058
1319885	Reep6	receptor accessory protein 6	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20180809	MGI			PMID:27889058
1319885	Reep6	receptor accessory protein 6	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20180809	MGI			PMID:27889058
1319885	Reep6	receptor accessory protein 6	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20180809	MGI			PMID:28475715
1319885	Reep6	receptor accessory protein 6	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20180809	MGI			PMID:28475715
1319885	Reep6	receptor accessory protein 6	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20180809	MGI			PMID:27889058
1319885	Reep6	receptor accessory protein 6	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20180809	MGI			PMID:28475715
1319885	Reep6	receptor accessory protein 6	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20180809	MGI			PMID:27889058
1319885	Reep6	receptor accessory protein 6	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20180809	MGI			PMID:28475715
1319885	Reep6	receptor accessory protein 6	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20180809	MGI			PMID:28475715
1319885	Reep6	receptor accessory protein 6	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:28475715
1319888	Gprc5b	G protein-coupled receptor, family C, group 5, member B	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20181227	MGI			
1319888	Gprc5b	G protein-coupled receptor, family C, group 5, member B	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1319888	Gprc5b	G protein-coupled receptor, family C, group 5, member B	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1319888	Gprc5b	G protein-coupled receptor, family C, group 5, member B	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1319888	Gprc5b	G protein-coupled receptor, family C, group 5, member B	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20170105	MGI			
1319888	Gprc5b	G protein-coupled receptor, family C, group 5, member B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1319888	Gprc5b	G protein-coupled receptor, family C, group 5, member B	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1319892	Crip3	cysteine-rich protein 3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713292
1319892	Crip3	cysteine-rich protein 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713292
1319892	Crip3	cysteine-rich protein 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1319892	Crip3	cysteine-rich protein 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713292
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065522
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065522
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065522
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20190131	MGI			PMID:19815523
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065522
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20190131	MGI			PMID:19815523
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20190314	MGI			PMID:19815523
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0006075	abnormal retina cone bipolar cell morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319894	Gnat2	G protein subunit alpha transducin 2	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20180712	MGI			PMID:23580486
1319896	Rad17	RAD17 checkpoint clamp loader component	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297881
1319896	Rad17	RAD17 checkpoint clamp loader component	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297881
1319896	Rad17	RAD17 checkpoint clamp loader component	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297881
1319896	Rad17	RAD17 checkpoint clamp loader component	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297881
1319896	Rad17	RAD17 checkpoint clamp loader component	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297881
1319896	Rad17	RAD17 checkpoint clamp loader component	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297881
1319896	Rad17	RAD17 checkpoint clamp loader component	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297881
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21769484
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21769484
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:21769484
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21769484
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21769484
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0005206	abnormal aqueous humor		IAGP		N	RGD:5509061	20141003	MGI			PMID:21769484
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0014165	absent ciliary process		IAGP		N	RGD:5509061	20160414	MGI			PMID:15728677
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0014175	abnormal ciliary epithelium morphology		IAGP		N	RGD:5509061	20160505	MGI			PMID:15728677
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0030138	abnormal lower incisor color		IAGP		N	RGD:5509061	20171005	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0030500	conical molar		IAGP		N	RGD:5509061	20180118	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0030522	abnormal stellate reticulum morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:21038445
1319898	Nectin3	nectin cell adhesion molecule 3	gene	MP:0030523	abnormal stratum intermedium morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:21038445
1319907	Cdk18	cyclin dependent kinase 18	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556483
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0002491	decreased IgD level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556483
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556483
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23509369
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556483
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556483
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12627171
1319912	Tab2	TGF-beta activated kinase 1/MAP3K7 binding protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22972987
1319916	Cisd1	CDGSH iron sulfur domain 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1319916	Cisd1	CDGSH iron sulfur domain 1	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20221215	MGI			
1319916	Cisd1	CDGSH iron sulfur domain 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376863
1319920	Maff	Maf bZIP transcription factor F	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10409670
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20808945
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20160804	MGI			
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0001324	abnormal eye pigmentation		IEA		N	RGD:5509061	20160804	MGI			
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103755
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20160804	MGI			
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0002697	abnormal eye size		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0002700	increased opacity of vitreous body		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103755
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0003671	abnormal eyelid aperture		IEA		N	RGD:5509061	20160804	MGI			
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103755
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160804	MGI			
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103755
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20171116	MGI			PMID:27310661
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20808945
1319929	Kat14	lysine acetyltransferase 14	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103755
1319935	Insm1	insulinoma-associated 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21284846
1319935	Insm1	insulinoma-associated 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0003972	decreased pituitary hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0004141	abnormal enteroendocrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0005128	decreased adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0005134	decreased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053427
1319935	Insm1	insulinoma-associated 1	gene	MP:0008330	absent somatotrophs		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0008339	absent thyrotrophs		IAGP		N	RGD:5509061	20141003	MGI			PMID:24227653
1319935	Insm1	insulinoma-associated 1	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21284846
1319935	Insm1	insulinoma-associated 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21284846
1319935	Insm1	insulinoma-associated 1	gene	MP:0009165	abnormal endocrine pancreas morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053427
1319935	Insm1	insulinoma-associated 1	gene	MP:0009169	pancreatic islet hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0009181	decreased pancreatic delta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0009185	increased PP cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0009187	absent PP cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0009191	decreased pancreatic epsilon cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21284846
1319935	Insm1	insulinoma-associated 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21284846
1319935	Insm1	insulinoma-associated 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21284846
1319935	Insm1	insulinoma-associated 1	gene	MP:0011400	lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1319935	Insm1	insulinoma-associated 1	gene	MP:0011910	decreased pancreatic endocrine progenitor cell proliferation		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053427
1319935	Insm1	insulinoma-associated 1	gene	MP:0011911	abnormal pancreatic endocrine progenitor cell physiology		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053427
1319935	Insm1	insulinoma-associated 1	gene	MP:0011932	abnormal endocrine pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319935	Insm1	insulinoma-associated 1	gene	MP:0011932	abnormal endocrine pancreas development		IAGP		N	RGD:5509061	20141120	MGI			PMID:25053427
1319935	Insm1	insulinoma-associated 1	gene	MP:0013220	increased pancreas apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951258
1319937	Ppp1r18	protein phosphatase 1, regulatory subunit 18	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20221215	MGI			PMID:35766979
1319937	Ppp1r18	protein phosphatase 1, regulatory subunit 18	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20221215	MGI			PMID:35766979
1319937	Ppp1r18	protein phosphatase 1, regulatory subunit 18	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20221215	MGI			PMID:35766979
1319937	Ppp1r18	protein phosphatase 1, regulatory subunit 18	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20221215	MGI			PMID:35766979
1319937	Ppp1r18	protein phosphatase 1, regulatory subunit 18	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20221215	MGI			PMID:35766979
1319937	Ppp1r18	protein phosphatase 1, regulatory subunit 18	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20221215	MGI			PMID:35766979
1319937	Ppp1r18	protein phosphatase 1, regulatory subunit 18	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20221215	MGI			PMID:35766979
1319937	Ppp1r18	protein phosphatase 1, regulatory subunit 18	gene	MP:0005387	immune system phenotype		IAGP		N	RGD:5509061	20221215	MGI			PMID:35766979
1319937	Ppp1r18	protein phosphatase 1, regulatory subunit 18	gene	MP:0020212	impaired leukocyte migration		IAGP		N	RGD:5509061	20221215	MGI			PMID:35766979
1319941	Zmym4	zinc finger, MYM-type 4	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1319941	Zmym4	zinc finger, MYM-type 4	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1319941	Zmym4	zinc finger, MYM-type 4	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1319941	Zmym4	zinc finger, MYM-type 4	gene	MP:0003443	increased circulating glycerol level		IEA		N	RGD:5509061	20210128	MGI			
1319941	Zmym4	zinc finger, MYM-type 4	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1319941	Zmym4	zinc finger, MYM-type 4	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1319941	Zmym4	zinc finger, MYM-type 4	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1319941	Zmym4	zinc finger, MYM-type 4	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1319941	Zmym4	zinc finger, MYM-type 4	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20201022	MGI			PMID:32492392
1319947	Cdyl2	chromodomain protein, Y chromosome-like 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20211021	MGI			
1319947	Cdyl2	chromodomain protein, Y chromosome-like 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20200514	MGI			
1319947	Cdyl2	chromodomain protein, Y chromosome-like 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1319947	Cdyl2	chromodomain protein, Y chromosome-like 2	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1319947	Cdyl2	chromodomain protein, Y chromosome-like 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20240523	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20170105	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20170105	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20190516	MGI			PMID:30626964
1319951	Setd3	SET domain containing 3	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20170105	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20170105	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20170105	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20220519	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0004514	dystocia		IAGP		N	RGD:5509061	20190516	MGI			PMID:30626964
1319951	Setd3	SET domain containing 3	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20201231	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20190516	MGI			PMID:30626964
1319951	Setd3	SET domain containing 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20170105	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20170105	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20190516	MGI			PMID:30626964
1319951	Setd3	SET domain containing 3	gene	MP:0020422	decreased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1319951	Setd3	SET domain containing 3	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200917	MGI			PMID:31527793
1319953	Nol8	nucleolar protein 8	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1319953	Nol8	nucleolar protein 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319953	Nol8	nucleolar protein 8	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1319956	Gga3	golgi associated, gamma adaptin ear containing, ARF binding protein 3	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1319956	Gga3	golgi associated, gamma adaptin ear containing, ARF binding protein 3	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1319956	Gga3	golgi associated, gamma adaptin ear containing, ARF binding protein 3	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1319956	Gga3	golgi associated, gamma adaptin ear containing, ARF binding protein 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1319956	Gga3	golgi associated, gamma adaptin ear containing, ARF binding protein 3	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1319956	Gga3	golgi associated, gamma adaptin ear containing, ARF binding protein 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1319956	Gga3	golgi associated, gamma adaptin ear containing, ARF binding protein 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22291915
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24023893
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24023893
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:24023893
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24023893
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24023893
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:24023893
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24023893
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24023893
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20240405	MGI			PMID:24086156
1319958	Lrig2	leucine-rich repeats and immunoglobulin-like domains 2	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:24086156
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1319961	Mrpl44	mitochondrial ribosomal protein L44	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260716	MGI			PMID:32376682
1319964	B3galt6	UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1319964	B3galt6	UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1319964	B3galt6	UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1319964	B3galt6	UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20160707	MGI			PMID:22508039
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733973
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733973
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733973
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733973
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733973
1319966	Gpr68	G protein-coupled receptor 68	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479052
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000151	absent ribs		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21404367
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0002758	long tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0008832	hemivertebra		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0008833	caudal hemivertebra		IAGP		N	RGD:5509061	20260219	MGI			PMID:38669183
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0008933	abnormal motile primary cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20160804	MGI			
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0010866	abnormal prenatal body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18296642
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1319968	Vangl1	VANGL planar cell polarity 1	gene	MP:0012027	abnormal embryonic cilium location or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562861
1319969	Rnf145	ring finger protein 145	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20260430	MGI			PMID:29068315
1319969	Rnf145	ring finger protein 145	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260430	MGI			PMID:29068315
1319969	Rnf145	ring finger protein 145	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20260430	MGI			PMID:29068315
1319969	Rnf145	ring finger protein 145	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20260430	MGI			PMID:29068315
1319969	Rnf145	ring finger protein 145	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20260430	MGI			PMID:29068315
1319969	Rnf145	ring finger protein 145	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1319973	Pbk	PDZ binding kinase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715333
1319973	Pbk	PDZ binding kinase	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715333
1319973	Pbk	PDZ binding kinase	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715333
1319973	Pbk	PDZ binding kinase	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20211021	MGI			PMID:32586419
1319973	Pbk	PDZ binding kinase	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715333
1319973	Pbk	PDZ binding kinase	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715333
1319973	Pbk	PDZ binding kinase	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715333
1319973	Pbk	PDZ binding kinase	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715333
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20250508	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0005356	positive geotaxis		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0010895	increased lung compliance		IEA		N	RGD:5509061	20250508	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0011045	decreased lung elastance		IEA		N	RGD:5509061	20250508	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0011625	cystolithiasis		IEA		N	RGD:5509061	20230601	MGI			
1319975	Plppr5	phospholipid phosphatase related 5	gene	MP:0020870	decreased thigmotaxis		IAGP		N	RGD:5509061	20220721	MGI			PMID:33692754
1319976	Akirin1	akirin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18066067
1319980	G3bp2	G3BP stress granule assembly factor 2	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20220915	MGI			PMID:35782098
1319980	G3bp2	G3BP stress granule assembly factor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319980	G3bp2	G3BP stress granule assembly factor 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220915	MGI			PMID:35782098
1319982	Aurkc	aurora kinase C	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192404
1319982	Aurkc	aurora kinase C	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192404
1319982	Aurkc	aurora kinase C	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192404
1319982	Aurkc	aurora kinase C	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192404
1319982	Aurkc	aurora kinase C	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192404
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682239
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682239
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19543268
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19543268
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19543268
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0003557	absent vas deferens		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0003558	absent uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0003576	oviduct hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19543268
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0003826	abnormal Mullerian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0004727	absent epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:11353389
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:15329828
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:3491125
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:7601909
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0009072	absent cranial vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0009073	absent Wolffian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054034
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19543268
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19543268
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0011843	abnormal kidney collecting duct epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19543268
1319984	Wnt9b	wingless-type MMTV integration site family, member 9B	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:21982646
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807889
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807889
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807889
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807889
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319986	Mia2	MIA SH3 domain ER export factor 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20190912	MGI			PMID:27311593
1319992	Dtnb	dystrobrevin, beta	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540561
1319992	Dtnb	dystrobrevin, beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585924
1319992	Dtnb	dystrobrevin, beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540561
1319992	Dtnb	dystrobrevin, beta	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540561
1319992	Dtnb	dystrobrevin, beta	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540561
1319998	Tfeb	transcription factor EB	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1319998	Tfeb	transcription factor EB	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20190502	MGI			
1319998	Tfeb	transcription factor EB	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1319998	Tfeb	transcription factor EB	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1319998	Tfeb	transcription factor EB	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1319998	Tfeb	transcription factor EB	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626501
1319998	Tfeb	transcription factor EB	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1319998	Tfeb	transcription factor EB	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1319998	Tfeb	transcription factor EB	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1319998	Tfeb	transcription factor EB	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1319998	Tfeb	transcription factor EB	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1319998	Tfeb	transcription factor EB	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240125	MGI			PMID:35662396
1319998	Tfeb	transcription factor EB	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1319998	Tfeb	transcription factor EB	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1319998	Tfeb	transcription factor EB	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1319998	Tfeb	transcription factor EB	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18438411
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18438411
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20211021	MGI			
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224918
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224918
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918981
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224918
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224918
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224918
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:18438411
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224918
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224918
1320000	Irak2	interleukin-1 receptor-associated kinase 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1320002	D1Pas1	DNA segment, Chr 1, Pasteur Institute 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20250424	MGI			PMID:39162228
1320002	D1Pas1	DNA segment, Chr 1, Pasteur Institute 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20250424	MGI			PMID:39162228
1320002	D1Pas1	DNA segment, Chr 1, Pasteur Institute 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250424	MGI			PMID:39162228
1320006	Sprr3	small proline-rich protein 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160630	MGI			PMID:25278290
1320006	Sprr3	small proline-rich protein 3	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1320006	Sprr3	small proline-rich protein 3	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20160630	MGI			PMID:25278290
1320006	Sprr3	small proline-rich protein 3	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20160630	MGI			PMID:25278290
1320006	Sprr3	small proline-rich protein 3	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:25278290
1320006	Sprr3	small proline-rich protein 3	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20160630	MGI			PMID:25278290
1320006	Sprr3	small proline-rich protein 3	gene	MP:0011436	decreased urine magnesium level		IEA		N	RGD:5509061	20211021	MGI			
1320011	Aopep	aminopeptidase O	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20200514	MGI			
1320011	Aopep	aminopeptidase O	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803194
1320011	Aopep	aminopeptidase O	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1320011	Aopep	aminopeptidase O	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20221215	MGI			
1320011	Aopep	aminopeptidase O	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1320013	Dlx1	distal-less homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1320013	Dlx1	distal-less homeobox 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1320013	Dlx1	distal-less homeobox 1	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:18697905
1320013	Dlx1	distal-less homeobox 1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1320013	Dlx1	distal-less homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1320013	Dlx1	distal-less homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1320013	Dlx1	distal-less homeobox 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1320013	Dlx1	distal-less homeobox 1	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20171005	MGI			PMID:18697905
1320013	Dlx1	distal-less homeobox 1	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1320013	Dlx1	distal-less homeobox 1	gene	MP:0004666	absent stapedial artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1320013	Dlx1	distal-less homeobox 1	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16632068
1320013	Dlx1	distal-less homeobox 1	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187081
1320013	Dlx1	distal-less homeobox 1	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1320013	Dlx1	distal-less homeobox 1	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1320013	Dlx1	distal-less homeobox 1	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1320013	Dlx1	distal-less homeobox 1	gene	MP:0009917	abnormal hyoid bone body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1320013	Dlx1	distal-less homeobox 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1320013	Dlx1	distal-less homeobox 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1320013	Dlx1	distal-less homeobox 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16632068
1320013	Dlx1	distal-less homeobox 1	gene	MP:0030127	small stapes		IAGP		N	RGD:5509061	20170928	MGI			PMID:9187081
1320013	Dlx1	distal-less homeobox 1	gene	MP:0030406	absent stapes obturator foramen		IAGP		N	RGD:5509061	20171207	MGI			PMID:9187081
1320017	Taf15	TATA-box binding protein associated factor 15	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1320017	Taf15	TATA-box binding protein associated factor 15	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1320017	Taf15	TATA-box binding protein associated factor 15	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1320017	Taf15	TATA-box binding protein associated factor 15	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000161	scoliosis		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000376	folliculitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20171207	MGI			PMID:28351661
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20171207	MGI			PMID:28351661
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20160915	MGI			PMID:27496731
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23972988
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20160915	MGI			PMID:27496731
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20160915	MGI			PMID:27496731
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20160915	MGI			PMID:27496731
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23972988
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160915	MGI			PMID:27496731
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002704	tubular nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23972988
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20160915	MGI			PMID:27496731
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003946	renal necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20160915	MGI			PMID:27496731
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284419
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23972988
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20171207	MGI			PMID:28351661
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005573	increased pulmonary respiratory rate		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20230105	MGI			PMID:36217001
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0010895	increased lung compliance		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0011045	decreased lung elastance		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0011048	decreased lung tissue damping		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20160804	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0011971	increased circulating lactate dehydrogenase level		IEA		N	RGD:5509061	20260402	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20241121	MGI			
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0014347	increased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:15254239
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:27496731
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0031054	bronchiolitis		IAGP		N	RGD:5509061	20200618	MGI			PMID:25848017
1320018	Trex1	three prime repair exonuclease 1	gene	MP:0031704	decreased interferon type I secretion		IAGP		N	RGD:5509061	20260402	MGI			PMID:27496731
1320020	Adam8	a disintegrin and metallopeptidase domain 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15580619
1320020	Adam8	a disintegrin and metallopeptidase domain 8	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19737139
1320020	Adam8	a disintegrin and metallopeptidase domain 8	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:20683884
1320020	Adam8	a disintegrin and metallopeptidase domain 8	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20683884
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210422	MGI			
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180222	MGI			PMID:28123425
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210422	MGI			
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180222	MGI			PMID:28123425
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0012051	spasticity		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20221103	MGI			
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20221103	MGI			
1320022	Ankfy1	ankyrin repeat and FYVE domain containing 1	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20190718	MGI			PMID:28588446
1320027	Lrrc8d	leucine rich repeat containing 8D	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1320027	Lrrc8d	leucine rich repeat containing 8D	gene	MP:0005387	immune system phenotype		IAGP		N	RGD:5509061	20201001	MGI			PMID:32277911
1320028	Tmem185b	transmembrane protein 185B	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20250508	MGI			
1320028	Tmem185b	transmembrane protein 185B	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1320031	Crygs	crystallin, gamma S	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121426
1320031	Crygs	crystallin, gamma S	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22715935
1320031	Crygs	crystallin, gamma S	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121426
1320031	Crygs	crystallin, gamma S	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:12079281
1320031	Crygs	crystallin, gamma S	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224648
1320031	Crygs	crystallin, gamma S	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:8812411
1320031	Crygs	crystallin, gamma S	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1320031	Crygs	crystallin, gamma S	gene	MP:0002579	disorganized secondary lens fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:6877261
1320031	Crygs	crystallin, gamma S	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121426
1320031	Crygs	crystallin, gamma S	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22715935
1320031	Crygs	crystallin, gamma S	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8812411
1320031	Crygs	crystallin, gamma S	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121426
1320031	Crygs	crystallin, gamma S	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:8812411
1320035	Nnmt	nicotinamide N-methyltransferase	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1320035	Nnmt	nicotinamide N-methyltransferase	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210128	MGI			
1320035	Nnmt	nicotinamide N-methyltransferase	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210128	MGI			
1320035	Nnmt	nicotinamide N-methyltransferase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1320035	Nnmt	nicotinamide N-methyltransferase	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20210128	MGI			
1320037	Emilin3	elastin microfibril interfacer 3	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1320037	Emilin3	elastin microfibril interfacer 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1320037	Emilin3	elastin microfibril interfacer 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1320040	Dapl1	death associated protein-like 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1320040	Dapl1	death associated protein-like 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20191128	MGI			PMID:28334846
1320040	Dapl1	death associated protein-like 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1320040	Dapl1	death associated protein-like 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1320040	Dapl1	death associated protein-like 1	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1320040	Dapl1	death associated protein-like 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20250508	MGI			
1320040	Dapl1	death associated protein-like 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20240523	MGI			
1320040	Dapl1	death associated protein-like 1	gene	MP:0005549	retina pigment epithelium hyperplasia		IAGP		N	RGD:5509061	20191128	MGI			PMID:28334846
1320040	Dapl1	death associated protein-like 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1320040	Dapl1	death associated protein-like 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20240523	MGI			
1320042	Pla2g2e	phospholipase A2, group IIE	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1320042	Pla2g2e	phospholipase A2, group IIE	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20241121	MGI			
1320042	Pla2g2e	phospholipase A2, group IIE	gene	MP:0011951	increased cardiac stroke volume		IEA		N	RGD:5509061	20211021	MGI			
1320042	Pla2g2e	phospholipase A2, group IIE	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1320048	Dtymk	deoxythymidylate kinase	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20240523	MGI			PMID:38621447
1320048	Dtymk	deoxythymidylate kinase	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20240523	MGI			PMID:38621447
1320054	Atp8a1	ATPase phospholipid transporting 8A1	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20141003	MGI			
1320054	Atp8a1	ATPase phospholipid transporting 8A1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1320054	Atp8a1	ATPase phospholipid transporting 8A1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
1320054	Atp8a1	ATPase phospholipid transporting 8A1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20160804	MGI			
1320054	Atp8a1	ATPase phospholipid transporting 8A1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20141003	MGI			
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000314	schistocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20111116	MGI			
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000704	abnormal thymus development		IEA		N	RGD:5509061	20111116	MGI			
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:1716634
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1716634
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1716634
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002095	abnormal skin pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002397	abnormal bone marrow morphology		IEA		N	RGD:5509061	20111116	MGI			
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10772878
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6234993
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236006
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1391963
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1391963
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236006
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1391963
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1391963
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10772878
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002814	hyperchromasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002830	gallstones		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002830	gallstones		IAGP		N	RGD:5509061	20141003	MGI			PMID:7410545
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003332	liver abscess		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7492791
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0004246	abnormal extensor digitorum longus morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005096	erythroblastosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1391963
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1391963
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008387	hypochromic anemia		IEA		N	RGD:5509061	20111116	MGI			
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008742	abnormal kidney iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1391963
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1391963
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008850	increased hemoglobin concentration distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0008956	decreased cellular hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0009411	abnormal skeletal muscle fiber triad morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0010035	increased erythrocyte clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0010074	stomatocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0010074	stomatocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0010163	hemolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0010163	hemolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0010177	acanthocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1832936
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011188	increased erythrocyte protoporphyrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:658175
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390527
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20151203	MGI			PMID:25354526
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:10772878
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:19179303
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:21193012
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:22723917
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:23934996
1320056	Ank1	ankyrin 1, erythroid	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:6763106
1320057	Resf1	retroelement silencing factor 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1320057	Resf1	retroelement silencing factor 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1320057	Resf1	retroelement silencing factor 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1320057	Resf1	retroelement silencing factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320064	Cdkl2	cyclin dependent kinase like 2	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210520	MGI			
1320064	Cdkl2	cyclin dependent kinase like 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1320064	Cdkl2	cyclin dependent kinase like 2	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1320064	Cdkl2	cyclin dependent kinase like 2	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20201022	MGI			
1320064	Cdkl2	cyclin dependent kinase like 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0011176	abnormal erythroblast morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0011898	abnormal platelet cell number		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320066	Pcbp2	poly(rC) binding protein 2	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1320067	Taf1d	TATA-box binding protein associated factor, RNA polymerase I, D	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1320067	Taf1d	TATA-box binding protein associated factor, RNA polymerase I, D	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1320067	Taf1d	TATA-box binding protein associated factor, RNA polymerase I, D	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1320067	Taf1d	TATA-box binding protein associated factor, RNA polymerase I, D	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0011344	abnormal loop of Henle ascending limb thick segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20180222	MGI			PMID:21685914
1320069	Prkcsh	protein kinase C substrate 80K-H	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320071	Midn	midnolin	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20111116	MGI			
1320071	Midn	midnolin	gene	MP:0001127	small ovary		IEA		N	RGD:5509061	20111116	MGI			
1320071	Midn	midnolin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1320071	Midn	midnolin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1320075	Kcna7	potassium voltage-gated channel, shaker-related subfamily, member 7	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220519	MGI			
1320075	Kcna7	potassium voltage-gated channel, shaker-related subfamily, member 7	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220519	MGI			
1320078	Fam193a	family with sequence homology 193, member A	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1320078	Fam193a	family with sequence homology 193, member A	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320081	Sorbs1	sorbin and SH3 domain containing 1	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351624
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15803212
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15803212
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550720
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15803212
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550720
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550720
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550720
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:15803212
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16329126
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16329126
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550720
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0006002	abnormal small intestinal transit time		IAGP		N	RGD:5509061	20141003	MGI			PMID:16329126
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9259577
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0009480	distended cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15803212
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0009480	distended cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0009485	distended ileum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9176491
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550720
1320083	Tlx2	T cell leukemia, homeobox 2	gene	MP:0011881	distended duodenum		IAGP		N	RGD:5509061	20150702	MGI			PMID:16329126
1320085	Guk1	guanylate kinase 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1320085	Guk1	guanylate kinase 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1320085	Guk1	guanylate kinase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20151217	MGI			PMID:24452334
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:33219378
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20160602	MGI			PMID:23281428
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20151217	MGI			PMID:24452334
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0001785	edema		IEA		N	RGD:5509061	20221215	MGI			
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20160602	MGI			PMID:23281428
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0002714	increased glycogen catabolism rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21035757
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20160602	MGI			PMID:23281428
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20160602	MGI			PMID:23281428
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20151217	MGI			PMID:24452334
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0004130	abnormal muscle cell glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21035757
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21035757
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0005439	decreased glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20151217	MGI			PMID:24452334
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21035757
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151126	MGI			PMID:25059425
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20221215	MGI			
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0012501	abnormal pericardial cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282316
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0014075	decreased brain glycogen level		IAGP		N	RGD:5509061	20160602	MGI			PMID:23281428
1320087	Gys1	glycogen synthase 1, muscle	gene	MP:0031007	decreased lung glycogen level		IAGP		N	RGD:5509061	20220331	MGI			PMID:33219378
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20250508	MGI			
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:1283314
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415348
1320089	Smarcad1	SNF2 related chromatin remodeling ATPase with DExD box 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320092	Adat2	adenosine deaminase, tRNA-specific 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20241121	MGI			
1320092	Adat2	adenosine deaminase, tRNA-specific 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20201231	MGI			
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0014329	abnormal Purkinje cell axon morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0030949	abnormal Golgi vesicle transport		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320093	Ap5z1	adaptor-related protein complex 5, zeta 1 subunit	gene	MP:0030952	abnormal Golgi stack morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30930081
1320097	Aga	aspartylglucosaminidase	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:8946839
1320097	Aga	aspartylglucosaminidase	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9425233
1320097	Aga	aspartylglucosaminidase	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9425233
1320097	Aga	aspartylglucosaminidase	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8946839
1320097	Aga	aspartylglucosaminidase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9425233
1320097	Aga	aspartylglucosaminidase	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0001655	multifocal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0003624	anuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0004195	abnormal kidney calyx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8946839
1320097	Aga	aspartylglucosaminidase	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9425233
1320097	Aga	aspartylglucosaminidase	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9686358
1320097	Aga	aspartylglucosaminidase	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0005302	neurogenic bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8946839
1320097	Aga	aspartylglucosaminidase	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9425233
1320097	Aga	aspartylglucosaminidase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10657992
1320097	Aga	aspartylglucosaminidase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8946839
1320097	Aga	aspartylglucosaminidase	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9425233
1320097	Aga	aspartylglucosaminidase	gene	MP:0011413	colorless urine		IAGP		N	RGD:5509061	20141003	MGI			PMID:9777961
1320097	Aga	aspartylglucosaminidase	gene	MP:0011516	aspartylglucosaminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:8946839
1320097	Aga	aspartylglucosaminidase	gene	MP:0011516	aspartylglucosaminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:9425233
1320099	Magel2	MAGE family member L2	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876615
1320099	Magel2	MAGE family member L2	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20230119	MGI			
1320099	Magel2	MAGE family member L2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893678
1320099	Magel2	MAGE family member L2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876615
1320099	Magel2	MAGE family member L2	gene	MP:0001752	abnormal hypothalamus secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876615
1320099	Magel2	MAGE family member L2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893678
1320099	Magel2	MAGE family member L2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0002679	abnormal corpus luteum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893678
1320099	Magel2	MAGE family member L2	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230119	MGI			
1320099	Magel2	MAGE family member L2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876615
1320099	Magel2	MAGE family member L2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230119	MGI			
1320099	Magel2	MAGE family member L2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20220630	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0009013	abnormal proestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876615
1320099	Magel2	MAGE family member L2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893678
1320099	Magel2	MAGE family member L2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19172181
1320099	Magel2	MAGE family member L2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876615
1320099	Magel2	MAGE family member L2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893678
1320099	Magel2	MAGE family member L2	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20160804	MGI			PMID:27436578
1320099	Magel2	MAGE family member L2	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:17893678
1320099	Magel2	MAGE family member L2	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20171012	MGI			PMID:17893678
1320102	Rlbp1	retinaldehyde binding protein 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301032
1320102	Rlbp1	retinaldehyde binding protein 1	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301032
1320102	Rlbp1	retinaldehyde binding protein 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301032
1320102	Rlbp1	retinaldehyde binding protein 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201231	MGI			
1320102	Rlbp1	retinaldehyde binding protein 1	gene	MP:0003011	delayed dark adaptation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301032
1320102	Rlbp1	retinaldehyde binding protein 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1320102	Rlbp1	retinaldehyde binding protein 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11301032
1320103	Efcab5	EF-hand calcium binding domain 5	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20220811	MGI			
1320103	Efcab5	EF-hand calcium binding domain 5	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1320103	Efcab5	EF-hand calcium binding domain 5	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20210520	MGI			
1320103	Efcab5	EF-hand calcium binding domain 5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1320103	Efcab5	EF-hand calcium binding domain 5	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1320103	Efcab5	EF-hand calcium binding domain 5	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20220811	MGI			
1320103	Efcab5	EF-hand calcium binding domain 5	gene	MP:0014803	abnormal flagellar waveform		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1320103	Efcab5	EF-hand calcium binding domain 5	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20260212	MGI			PMID:40931011
1320104	Clmb	calcimembrin	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20260409	MGI			PMID:40355556
1320104	Clmb	calcimembrin	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20260409	MGI			PMID:40355556
1320104	Clmb	calcimembrin	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20260409	MGI			PMID:40355556
1320104	Clmb	calcimembrin	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20260409	MGI			PMID:40355556
1320104	Clmb	calcimembrin	gene	MP:0011019	abnormal adaptive thermogenesis		IAGP		N	RGD:5509061	20260409	MGI			PMID:40355556
1320104	Clmb	calcimembrin	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20260409	MGI			PMID:40355556
1320104	Clmb	calcimembrin	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20260409	MGI			PMID:40355556
1320104	Clmb	calcimembrin	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20260409	MGI			PMID:40355556
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133777
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20210429	MGI			PMID:32938684
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20210429	MGI			PMID:32938684
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133777
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20210429	MGI			PMID:32938684
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20210429	MGI			PMID:32938684
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0012207	decreased neuronal stem cell self-renewal		IAGP		N	RGD:5509061	20210429	MGI			PMID:32938684
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:32938684
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32938684
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0020358	abnormal inhibitory synapse morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32938684
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0030707	decreased glutamine level		IAGP		N	RGD:5509061	20210429	MGI			PMID:32938684
1320108	Ptprt	protein tyrosine phosphatase receptor type T	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20210429	MGI			PMID:32938684
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20221215	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20241121	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210826	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210826	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20210826	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210826	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20210826	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20210826	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20210826	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20230601	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20220519	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1320110	Sox14	SRY (sex determining region Y)-box 14	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210826	MGI			
1320111	Cep95	centrosomal protein 95	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201231	MGI			
1320111	Cep95	centrosomal protein 95	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201022	MGI			
1320111	Cep95	centrosomal protein 95	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1320112	Tapt1	transmembrane anterior posterior transformation 1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20111116	MGI			
1320112	Tapt1	transmembrane anterior posterior transformation 1	gene	MP:0001577	anemia		IEA		N	RGD:5509061	20111116	MGI			
1320112	Tapt1	transmembrane anterior posterior transformation 1	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17151244
1320112	Tapt1	transmembrane anterior posterior transformation 1	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17151244
1320112	Tapt1	transmembrane anterior posterior transformation 1	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:17151244
1320112	Tapt1	transmembrane anterior posterior transformation 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1320112	Tapt1	transmembrane anterior posterior transformation 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1320112	Tapt1	transmembrane anterior posterior transformation 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17151244
1320112	Tapt1	transmembrane anterior posterior transformation 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1320116	Snai3	snail family zinc finger 3	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23762348
1320116	Snai3	snail family zinc finger 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150409	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0014129	thymus fibrosis		IAGP		N	RGD:5509061	20160324	MGI			PMID:23874916
1320116	Snai3	snail family zinc finger 3	gene	MP:0014350	disorganized spleen B cell follicle		IAGP		N	RGD:5509061	20240104	MGI			PMID:23874916
1320118	Arrdc2	arrestin domain containing 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1320118	Arrdc2	arrestin domain containing 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1320118	Arrdc2	arrestin domain containing 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20221215	MGI			
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20250508	MGI			
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0003631	nervous system phenotype		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0005390	skeleton phenotype		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0005391	vision/eye phenotype		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0009268	absent cerebellum fissure		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1320119	Tmem161b	transmembrane protein 161B	gene	MP:0030192	downturned snout		IAGP		N	RGD:5509061	20230907	MGI			PMID:36669109
1320121	Klhl5	kelch-like 5	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20200514	MGI			
1320121	Klhl5	kelch-like 5	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20210128	MGI			
1320121	Klhl5	kelch-like 5	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20200514	MGI			
1320121	Klhl5	kelch-like 5	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1320121	Klhl5	kelch-like 5	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200514	MGI			
1320121	Klhl5	kelch-like 5	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1320121	Klhl5	kelch-like 5	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1320121	Klhl5	kelch-like 5	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1320121	Klhl5	kelch-like 5	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
1320123	E2f3	E2F transcription factor 3	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663357
1320123	E2f3	E2F transcription factor 3	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663357
1320123	E2f3	E2F transcription factor 3	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733529
1320123	E2f3	E2F transcription factor 3	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663357
1320123	E2f3	E2F transcription factor 3	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20241121	MGI			
1320123	E2f3	E2F transcription factor 3	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201231	MGI			
1320123	E2f3	E2F transcription factor 3	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663357
1320123	E2f3	E2F transcription factor 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1320123	E2f3	E2F transcription factor 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210826	MGI			
1320123	E2f3	E2F transcription factor 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200402	MGI			
1320123	E2f3	E2F transcription factor 3	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663357
1320123	E2f3	E2F transcription factor 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0002679	abnormal corpus luteum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663357
1320123	E2f3	E2F transcription factor 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733529
1320123	E2f3	E2F transcription factor 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663357
1320123	E2f3	E2F transcription factor 3	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1320123	E2f3	E2F transcription factor 3	gene	MP:0004002	abnormal jejunum morphology		IEA		N	RGD:5509061	20210826	MGI			
1320123	E2f3	E2F transcription factor 3	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0005158	ovary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1320123	E2f3	E2F transcription factor 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733529
1320123	E2f3	E2F transcription factor 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11511364
1320123	E2f3	E2F transcription factor 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663357
1320123	E2f3	E2F transcription factor 3	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1320123	E2f3	E2F transcription factor 3	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1320123	E2f3	E2F transcription factor 3	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608565
1320123	E2f3	E2F transcription factor 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0010334	pleural effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733529
1320123	E2f3	E2F transcription factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663357
1320123	E2f3	E2F transcription factor 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594513
1320123	E2f3	E2F transcription factor 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320123	E2f3	E2F transcription factor 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11511364
1320123	E2f3	E2F transcription factor 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11909960
1320123	E2f3	E2F transcription factor 3	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:11909960
1320125	Pdcl3	phosducin-like 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0012174	flat head		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320132	Sf3b4	splicing factor 3b, subunit 4	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31900962
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20180920	MGI			PMID:21247897
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180920	MGI			PMID:21247897
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20180920	MGI			PMID:21247897
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:30653527
1320133	Dcun1d1	defective in cullin neddylation 1 domain containing 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20180920	MGI			PMID:21247897
1320135	Dnal1	dynein, axonemal, light chain 1	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20170504	MGI			
1320135	Dnal1	dynein, axonemal, light chain 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1320135	Dnal1	dynein, axonemal, light chain 1	gene	MP:0002581	abnormal ileum morphology		IEA		N	RGD:5509061	20170504	MGI			
1320135	Dnal1	dynein, axonemal, light chain 1	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20210520	MGI			
1320135	Dnal1	dynein, axonemal, light chain 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20170504	MGI			
1320135	Dnal1	dynein, axonemal, light chain 1	gene	MP:0010378	increased respiratory quotient		IEA		N	RGD:5509061	20210128	MGI			
1320135	Dnal1	dynein, axonemal, light chain 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170504	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20210520	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210826	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20201022	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20201022	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210520	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210128	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1320137	Zfp236	zinc finger protein 236	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1320143	P4ha2	procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha II polypeptide	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1320145	Sox13	SRY (sex determining region Y)-box 13	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218525
1320145	Sox13	SRY (sex determining region Y)-box 13	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218525
1320145	Sox13	SRY (sex determining region Y)-box 13	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1320145	Sox13	SRY (sex determining region Y)-box 13	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218525
1320145	Sox13	SRY (sex determining region Y)-box 13	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1320145	Sox13	SRY (sex determining region Y)-box 13	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218525
1320149	Prxl2a	peroxiredoxin like 2A	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20161027	MGI			PMID:26629401
1320149	Prxl2a	peroxiredoxin like 2A	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20161027	MGI			PMID:26629401
1320149	Prxl2a	peroxiredoxin like 2A	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20161027	MGI			PMID:26629401
1320149	Prxl2a	peroxiredoxin like 2A	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20161027	MGI			PMID:26629401
1320149	Prxl2a	peroxiredoxin like 2A	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20161027	MGI			PMID:26629401
1320149	Prxl2a	peroxiredoxin like 2A	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:26629401
1320149	Prxl2a	peroxiredoxin like 2A	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:26629401
1320151	Cd83	CD83 antigen	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20241121	MGI			
1320151	Cd83	CD83 antigen	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20241121	MGI			
1320151	Cd83	CD83 antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701714
1320151	Cd83	CD83 antigen	gene	MP:0004939	abnormal B cell morphology		IEA		N	RGD:5509061	20111116	MGI			
1320151	Cd83	CD83 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322158
1320151	Cd83	CD83 antigen	gene	MP:0005461	abnormal dendritic cell morphology		IEA		N	RGD:5509061	20111116	MGI			
1320151	Cd83	CD83 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322158
1320151	Cd83	CD83 antigen	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322158
1320151	Cd83	CD83 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170706	MGI			PMID:27503071
1320151	Cd83	CD83 antigen	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322158
1320151	Cd83	CD83 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320151	Cd83	CD83 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955430
1320153	Colec11	collectin sub-family member 11	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:27088797
1320153	Colec11	collectin sub-family member 11	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20170706	MGI			PMID:27088797
1320153	Colec11	collectin sub-family member 11	gene	MP:0005265	abnormal blood urea nitrogen level		IAGP		N	RGD:5509061	20170706	MGI			PMID:27088797
1320153	Colec11	collectin sub-family member 11	gene	MP:0011566	abnormal complement protein level		IAGP		N	RGD:5509061	20170706	MGI			PMID:27088797
1320155	Thap12	THAP domain containing 12	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1320155	Thap12	THAP domain containing 12	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1320155	Thap12	THAP domain containing 12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1320155	Thap12	THAP domain containing 12	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20250508	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413500
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20241121	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10864874
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10864874
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16636276
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360665
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20201022	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10864874
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20241121	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20241121	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0003194	abnormal frequency of paradoxical sleep		IAGP		N	RGD:5509061	20141003	MGI			PMID:16636276
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360665
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413500
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360665
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413500
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0005661	decreased circulating adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360665
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0005664	decreased circulating noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360665
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0014624	abnormal brain delta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:16636276
1320158	Npas2	neuronal PAS domain protein 2	gene	MP:0014639	decreased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:16636276
1320159	Tmem209	transmembrane protein 209	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20181227	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20181227	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20210520	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230601	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20181227	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20230601	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0009263	abnormal eyelid fusion		IEA		N	RGD:5509061	20221215	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0009908	protruding tongue		IEA		N	RGD:5509061	20221215	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20221215	MGI			
1320159	Tmem209	transmembrane protein 209	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20221215	MGI			
1320160	Ppme1	protein phosphatase methylesterase 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1320160	Ppme1	protein phosphatase methylesterase 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18596935
1320160	Ppme1	protein phosphatase methylesterase 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1320160	Ppme1	protein phosphatase methylesterase 1	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18596935
1320160	Ppme1	protein phosphatase methylesterase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18596935
1320160	Ppme1	protein phosphatase methylesterase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18596935
1320160	Ppme1	protein phosphatase methylesterase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622869
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0001192	scaly skin		IEA		N	RGD:5509061	20210520	MGI			
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622869
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622870
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0009286	increased abdominal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622870
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20250508	MGI			
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0010095	increased chromosomal stability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622869
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0010207	abnormal telomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622869
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20622870
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0011117	abnormal susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170202	MGI			PMID:23791522
1320162	Terf2ip	telomeric repeat binding factor 2, interacting protein	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:20622869
1320163	Mif4gd	MIF4G domain containing	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
1320163	Mif4gd	MIF4G domain containing	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1320169	Pprc1	peroxisome proliferative activated receptor, gamma, coactivator-related 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411706
1320169	Pprc1	peroxisome proliferative activated receptor, gamma, coactivator-related 1	gene	MP:0003695	delayed blastocyst hatching from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411706
1320169	Pprc1	peroxisome proliferative activated receptor, gamma, coactivator-related 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411706
1320169	Pprc1	peroxisome proliferative activated receptor, gamma, coactivator-related 1	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411706
1320169	Pprc1	peroxisome proliferative activated receptor, gamma, coactivator-related 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22411706
1320171	Polr1c	polymerase (RNA) I polypeptide C	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1320171	Polr1c	polymerase (RNA) I polypeptide C	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20241121	MGI			
1320171	Polr1c	polymerase (RNA) I polypeptide C	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201231	MGI			
1320171	Polr1c	polymerase (RNA) I polypeptide C	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210128	MGI			
1320171	Polr1c	polymerase (RNA) I polypeptide C	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20210128	MGI			
1320171	Polr1c	polymerase (RNA) I polypeptide C	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1320171	Polr1c	polymerase (RNA) I polypeptide C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320171	Polr1c	polymerase (RNA) I polypeptide C	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0010147	abnormal endocrine pancreas physiology		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0014117	increased pancreatic beta cell apoptosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:32640216
1320174	Jazf1	JAZF zinc finger 1	gene	MP:0031739	impaired translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:32640216
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20181206	MGI			PMID:28655741
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20181206	MGI			PMID:29116018
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20150528	MGI			PMID:12573256
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20200827	MGI			PMID:32646486
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20150528	MGI			PMID:12573256
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20181206	MGI			PMID:28655741
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20181206	MGI			PMID:29116018
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20220602	MGI			PMID:10425919
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:28128203
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246778
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20150528	MGI			PMID:12573256
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20181206	MGI			PMID:28655741
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20181206	MGI			PMID:29116018
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20220602	MGI			PMID:10425919
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001214	skin hyperplasia		IAGP		N	RGD:5509061	20181206	MGI			PMID:28655741
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001214	skin hyperplasia		IAGP		N	RGD:5509061	20181206	MGI			PMID:29116018
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20220519	MGI			PMID:28128203
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20150528	MGI			PMID:12573256
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20181206	MGI			PMID:28655741
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20181206	MGI			PMID:29116018
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:12573256
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20150528	MGI			PMID:12573256
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20200827	MGI			PMID:32646486
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20210128	MGI			
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001790	abnormal immune system physiology		IEA		N	RGD:5509061	20141003	MGI			
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220602	MGI			PMID:10425919
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20181206	MGI			PMID:28655741
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20210128	MGI			
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246778
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246778
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246778
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20181206	MGI			PMID:28655741
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20181206	MGI			PMID:29116018
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20181206	MGI			PMID:28655741
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20181206	MGI			PMID:29116018
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:12573256
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20220602	MGI			PMID:10425919
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220602	MGI			PMID:10425919
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20220602	MGI			PMID:10425919
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246777
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246778
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246777
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246778
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550345
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0009273	abnormal hair shaft melanin granule shape		IAGP		N	RGD:5509061	20150528	MGI			PMID:12573256
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0009786	decreased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246778
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246778
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20211021	MGI			
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0010600	enlarged pulmonary valve		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0010605	thick pulmonary valve cusps		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0010626	thick tricuspid valve cusps		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0010627	enlarged tricuspid valve		IAGP		N	RGD:5509061	20161103	MGI			PMID:25918388
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:12573256
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23969955
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20181206	MGI			PMID:29116018
1320183	Rhbdf2	rhomboid 5 homolog 2	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240418	MGI			PMID:12573256
1320184	Smg5	SMG5 nonsense mediated mRNA decay factor	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1320184	Smg5	SMG5 nonsense mediated mRNA decay factor	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1320184	Smg5	SMG5 nonsense mediated mRNA decay factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20240926	MGI			PMID:39199410
1320184	Smg5	SMG5 nonsense mediated mRNA decay factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320184	Smg5	SMG5 nonsense mediated mRNA decay factor	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1320184	Smg5	SMG5 nonsense mediated mRNA decay factor	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1320185	Fam114a1	family with sequence similarity 114, member A1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1320185	Fam114a1	family with sequence similarity 114, member A1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20170518	MGI			PMID:25611509
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1320188	Adgrb3	adhesion G protein-coupled receptor B3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0001575	cyanosis		IEA		N	RGD:5509061	20210520	MGI			
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320190	Bclaf1	BCL2-associated transcription factor 1	gene	MP:0011145	abnormal mesenchymal cell differentiation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008920
1320193	Vcf1	VCP nuclear cofactor family member 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1320193	Vcf1	VCP nuclear cofactor family member 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0030980	abnormal acroplaxome morphology		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320195	Ccdc181	coiled-coil domain containing 181	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20241219	MGI			PMID:39245650
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0031204	hindlimb paresis		IAGP		N	RGD:5509061	20210218	MGI			PMID:9600738
1320202	Cln6	ceroid-lipofuscinosis, neuronal 6	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:9600738
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20160421	MGI			
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220519	MGI			
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0004152	abnormal circulating iron level		IAGP		N	RGD:5509061	20161117	MGI			PMID:27048792
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20161117	MGI			PMID:27048792
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0008738	abnormal liver iron level		IAGP		N	RGD:5509061	20161117	MGI			PMID:27048792
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20161117	MGI			PMID:27048792
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20161117	MGI			PMID:27048792
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1320206	Ndfip2	Nedd4 family interacting protein 2	gene	MP:0011895	abnormal circulating unsaturated transferrin level		IAGP		N	RGD:5509061	20161117	MGI			PMID:27048792
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0012023	decreased melanocyte number		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320215	Afg3l1	AFG3-like AAA ATPase 1	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20170126	MGI			PMID:27911893
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116426
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0002632	vestigial tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004407	increased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116426
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116426
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116426
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12421720
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008950
1320220	Dvl2	dishevelled segment polarity protein 2	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571627
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19564410
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875667
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875667
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19564410
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875667
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19564410
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875667
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19564410
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875667
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17875667
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0003234	enhanced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0004495	decreased synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19564410
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048139
1320223	Mapk8ip2	mitogen-activated protein kinase 8 interacting protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19564410
1320225	Cbr3	carbonyl reductase 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1320225	Cbr3	carbonyl reductase 3	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1320225	Cbr3	carbonyl reductase 3	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1320225	Cbr3	carbonyl reductase 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1320225	Cbr3	carbonyl reductase 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1320225	Cbr3	carbonyl reductase 3	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1320225	Cbr3	carbonyl reductase 3	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1320225	Cbr3	carbonyl reductase 3	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1320226	Fastkd3	FAST kinase domains 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1320226	Fastkd3	FAST kinase domains 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1320227	Iftap	intraflagellar transport associated protein	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20201224	MGI			PMID:30521625
1320227	Iftap	intraflagellar transport associated protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20201224	MGI			PMID:30521625
1320227	Iftap	intraflagellar transport associated protein	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20201224	MGI			PMID:30521625
1320227	Iftap	intraflagellar transport associated protein	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:30521625
1320227	Iftap	intraflagellar transport associated protein	gene	MP:0009697	abnormal copulation behavior		IAGP		N	RGD:5509061	20201224	MGI			PMID:30521625
1320228	Mtss2	MTSS I-BAR domain containing 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1320228	Mtss2	MTSS I-BAR domain containing 2	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20200402	MGI			
1320230	Matn4	matrilin 4	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1320230	Matn4	matrilin 4	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1320230	Matn4	matrilin 4	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1320230	Matn4	matrilin 4	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1320230	Matn4	matrilin 4	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1320230	Matn4	matrilin 4	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1320230	Matn4	matrilin 4	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1320232	Nlrp9a	NLR family, pyrin domain containing 9A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1320232	Nlrp9a	NLR family, pyrin domain containing 9A	gene	MP:0002293	long gestation period		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1320232	Nlrp9a	NLR family, pyrin domain containing 9A	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1320232	Nlrp9a	NLR family, pyrin domain containing 9A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1320232	Nlrp9a	NLR family, pyrin domain containing 9A	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1320232	Nlrp9a	NLR family, pyrin domain containing 9A	gene	MP:0012128	abnormal blastocyst formation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1320232	Nlrp9a	NLR family, pyrin domain containing 9A	gene	MP:0012129	failure of blastocyst formation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32413845
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20201231	MGI			
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20200514	MGI			
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20210520	MGI			
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20200514	MGI			
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1320233	Lamtor4	late endosomal/lysosomal adaptor, MAPK and MTOR activator 4	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210520	MGI			
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12955145
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0004081	abnormal globus pallidus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548961
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:23077216
1320235	Zdhhc13	zinc finger, DHHC domain containing 13	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:23077216
1320239	Caskin2	CASK-interacting protein 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1320239	Caskin2	CASK-interacting protein 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20210603	MGI			PMID:31727973
1320239	Caskin2	CASK-interacting protein 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20210603	MGI			PMID:31727973
1320239	Caskin2	CASK-interacting protein 2	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20211021	MGI			
1320239	Caskin2	CASK-interacting protein 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1320239	Caskin2	CASK-interacting protein 2	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20210603	MGI			PMID:31727973
1320239	Caskin2	CASK-interacting protein 2	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:31727973
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000265	blood vessel atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20231116	MGI			PMID:33899511
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231116	MGI			PMID:33899511
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21498671
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824583
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824583
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21598246
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824583
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0002748	abnormal pulmonary valve morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:33899511
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003228	abnormal sinus venosus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003230	abnormal umbilical artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003410	abnormal artery development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003411	abnormal vein development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824583
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004786	abnormal common cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824583
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0006093	arteriovenous malformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231116	MGI			PMID:33899511
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18824585
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21498671
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231116	MGI			PMID:33899511
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0010463	aorta stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0012501	abnormal pericardial cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466159
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0012730	abnormal internal carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320242	Dll4	delta like canonical Notch ligand 4	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520367
1320246	Crtap	cartilage associated protein	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055431
1320246	Crtap	cartilage associated protein	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:17055431
1320250	Zfp638	zinc finger protein 638	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1320250	Zfp638	zinc finger protein 638	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20230601	MGI			
1320250	Zfp638	zinc finger protein 638	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1320250	Zfp638	zinc finger protein 638	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1320252	Hapstr1	HUWE1 associated protein modifying stress responses	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1320252	Hapstr1	HUWE1 associated protein modifying stress responses	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1320252	Hapstr1	HUWE1 associated protein modifying stress responses	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1320252	Hapstr1	HUWE1 associated protein modifying stress responses	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1320252	Hapstr1	HUWE1 associated protein modifying stress responses	gene	MP:0009480	distended cecum		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1320252	Hapstr1	HUWE1 associated protein modifying stress responses	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1320252	Hapstr1	HUWE1 associated protein modifying stress responses	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1320252	Hapstr1	HUWE1 associated protein modifying stress responses	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1320253	Trim16	tripartite motif-containing 16	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1320253	Trim16	tripartite motif-containing 16	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20201231	MGI			PMID:31342168
1320253	Trim16	tripartite motif-containing 16	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1320253	Trim16	tripartite motif-containing 16	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1320253	Trim16	tripartite motif-containing 16	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20201231	MGI			PMID:31342168
1320253	Trim16	tripartite motif-containing 16	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20201231	MGI			PMID:31342168
1320253	Trim16	tripartite motif-containing 16	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20201022	MGI			
1320253	Trim16	tripartite motif-containing 16	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20201231	MGI			PMID:31342168
1320256	Tfg	Trk-fused gene	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20250508	MGI			
1320256	Tfg	Trk-fused gene	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20260402	MGI			
1320256	Tfg	Trk-fused gene	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20260402	MGI			
1320256	Tfg	Trk-fused gene	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20260402	MGI			
1320256	Tfg	Trk-fused gene	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20260402	MGI			
1320256	Tfg	Trk-fused gene	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1320256	Tfg	Trk-fused gene	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20260402	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20240822	MGI			PMID:36053215
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0003271	abnormal duodenum morphology		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20240822	MGI			PMID:36053215
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0004882	enlarged lung		IEA		N	RGD:5509061	20230601	MGI			
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20240822	MGI			PMID:36053215
1320259	Vamp4	vesicle-associated membrane protein 4	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20240822	MGI			PMID:36053215
1320261	Slfn1	schlafen 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9846487
1320261	Slfn1	schlafen 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1320261	Slfn1	schlafen 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1320261	Slfn1	schlafen 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1320263	Rgl3	ral guanine nucleotide dissociation stimulator-like 3	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1320263	Rgl3	ral guanine nucleotide dissociation stimulator-like 3	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1320263	Rgl3	ral guanine nucleotide dissociation stimulator-like 3	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1320265	Cd72	CD72 antigen	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0004795	decreased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0004798	decreased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0006315	abnormal urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:10549631
1320265	Cd72	CD72 antigen	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:23616572
1320265	Cd72	CD72 antigen	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:23616572
1320267	Exosc7	exosome component 7	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1320267	Exosc7	exosome component 7	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1320267	Exosc7	exosome component 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1320269	Ginm1	glycoprotein integral membrane 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1320269	Ginm1	glycoprotein integral membrane 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1320269	Ginm1	glycoprotein integral membrane 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1320269	Ginm1	glycoprotein integral membrane 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1320269	Ginm1	glycoprotein integral membrane 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1320271	Traip	TRAF-interacting protein	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927961
1320271	Traip	TRAF-interacting protein	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927961
1320271	Traip	TRAF-interacting protein	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927961
1320271	Traip	TRAF-interacting protein	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927961
1320271	Traip	TRAF-interacting protein	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927961
1320271	Traip	TRAF-interacting protein	gene	MP:0011198	absent proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17927961
1320271	Traip	TRAF-interacting protein	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17927961
1320274	Snx4	sorting nexin 4	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20251009	MGI			PMID:39699951
1320274	Snx4	sorting nexin 4	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20251009	MGI			PMID:39699951
1320274	Snx4	sorting nexin 4	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20251009	MGI			PMID:39699951
1320274	Snx4	sorting nexin 4	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20251009	MGI			PMID:39699951
1320274	Snx4	sorting nexin 4	gene	MP:0015052	abnormal presynaptic active zone morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:39699951
1320274	Snx4	sorting nexin 4	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:39699951
1320276	Trappc11	trafficking protein particle complex 11	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1320276	Trappc11	trafficking protein particle complex 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1320276	Trappc11	trafficking protein particle complex 11	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1320281	Ahcyl1	S-adenosylhomocysteine hydrolase-like 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20150108	MGI			
1320281	Ahcyl1	S-adenosylhomocysteine hydrolase-like 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1320281	Ahcyl1	S-adenosylhomocysteine hydrolase-like 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1320281	Ahcyl1	S-adenosylhomocysteine hydrolase-like 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1320281	Ahcyl1	S-adenosylhomocysteine hydrolase-like 1	gene	MP:0005477	increased circulating thyroxine level		IEA		N	RGD:5509061	20210128	MGI			
1320281	Ahcyl1	S-adenosylhomocysteine hydrolase-like 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1320281	Ahcyl1	S-adenosylhomocysteine hydrolase-like 1	gene	MP:0010148	abnormal exocrine pancreas physiology		IAGP		N	RGD:5509061	20151119	MGI			PMID:23542070
1320283	Bbx	bobby sox HMG box containing	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1320283	Bbx	bobby sox HMG box containing	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20160804	MGI			
1320283	Bbx	bobby sox HMG box containing	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1320283	Bbx	bobby sox HMG box containing	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1320283	Bbx	bobby sox HMG box containing	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1320283	Bbx	bobby sox HMG box containing	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1320283	Bbx	bobby sox HMG box containing	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1320283	Bbx	bobby sox HMG box containing	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1320283	Bbx	bobby sox HMG box containing	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1320283	Bbx	bobby sox HMG box containing	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1320283	Bbx	bobby sox HMG box containing	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1320285	Adamts15	ADAM metallopeptidase with thrombospondin type 1 motif 15	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1320285	Adamts15	ADAM metallopeptidase with thrombospondin type 1 motif 15	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20231207	MGI			
1320285	Adamts15	ADAM metallopeptidase with thrombospondin type 1 motif 15	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1320285	Adamts15	ADAM metallopeptidase with thrombospondin type 1 motif 15	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20181227	MGI			
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0009388	abnormal epidermal melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21674502
1320287	Rpl27a	ribosomal protein L27A	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21674502
1320289	Api5	apoptosis inhibitor 5	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1320289	Api5	apoptosis inhibitor 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1320289	Api5	apoptosis inhibitor 5	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320292	Zcchc8	zinc finger, CCHC domain containing 8	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20210610	MGI			PMID:31747613
1320296	Il7r	interleukin 7 receptor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964471
1320296	Il7r	interleukin 7 receptor	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267098
1320296	Il7r	interleukin 7 receptor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11034372
1320296	Il7r	interleukin 7 receptor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11123301
1320296	Il7r	interleukin 7 receptor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964471
1320296	Il7r	interleukin 7 receptor	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964471
1320296	Il7r	interleukin 7 receptor	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964471
1320296	Il7r	interleukin 7 receptor	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509509
1320296	Il7r	interleukin 7 receptor	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20303297
1320296	Il7r	interleukin 7 receptor	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488150
1320296	Il7r	interleukin 7 receptor	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267098
1320296	Il7r	interleukin 7 receptor	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964471
1320296	Il7r	interleukin 7 receptor	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964471
1320296	Il7r	interleukin 7 receptor	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11123301
1320296	Il7r	interleukin 7 receptor	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267098
1320296	Il7r	interleukin 7 receptor	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267098
1320296	Il7r	interleukin 7 receptor	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267098
1320296	Il7r	interleukin 7 receptor	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325202
1320296	Il7r	interleukin 7 receptor	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109710
1320296	Il7r	interleukin 7 receptor	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267098
1320296	Il7r	interleukin 7 receptor	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7964471
1320296	Il7r	interleukin 7 receptor	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:32457448
1320296	Il7r	interleukin 7 receptor	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267098
1320296	Il7r	interleukin 7 receptor	gene	MP:0008355	absent mature gamma-delta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0008356	abnormal gamma-delta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8692964
1320296	Il7r	interleukin 7 receptor	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20250731	MGI			PMID:32457448
1320296	Il7r	interleukin 7 receptor	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11123301
1320298	Mrc2	mannose receptor, C type 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668656
1320298	Mrc2	mannose receptor, C type 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17596337
1320298	Mrc2	mannose receptor, C type 2	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12835757
1320300	Snx13	sorting nexin 13	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1320300	Snx13	sorting nexin 13	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077144
1320300	Snx13	sorting nexin 13	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1320301	2300009A05Rik	RIKEN cDNA 2300009A05 gene	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1320303	Ca1	carbonic anhydrase 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20241003	MGI			PMID:37013604
1320303	Ca1	carbonic anhydrase 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20241003	MGI			PMID:37013604
1320303	Ca1	carbonic anhydrase 1	gene	MP:0008269	abnormal hippocampus CA4 region morphology		IAGP		N	RGD:5509061	20241003	MGI			PMID:37013604
1320303	Ca1	carbonic anhydrase 1	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20241003	MGI			PMID:37013604
1320303	Ca1	carbonic anhydrase 1	gene	MP:0014414	increased depression-related behavior		IAGP		N	RGD:5509061	20241003	MGI			PMID:37013604
1320303	Ca1	carbonic anhydrase 1	gene	MP:0021009	abnormal synaptic physiology		IAGP		N	RGD:5509061	20241003	MGI			PMID:37013604
1320307	Eed	embryonic ectoderm development	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19941827
1320307	Eed	embryonic ectoderm development	gene	MP:0000371	diluted coat color		IEA		N	RGD:5509061	20111116	MGI			
1320307	Eed	embryonic ectoderm development	gene	MP:0002427	disproportionate dwarf		IEA		N	RGD:5509061	20111116	MGI			
1320312	Tprkb	Tp53rk binding protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20221124	MGI			PMID:34849815
1320312	Tprkb	Tp53rk binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11340172
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11340172
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11340172
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11340172
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11340172
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11340172
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0003415	priapism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11340172
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446783
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446783
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11340172
1320314	Stam	signal transducing adaptor molecule (SH3 domain and ITAM motif) 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446783
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200716	MGI			PMID:31916570
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220811	MGI			PMID:34388164
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20200716	MGI			PMID:31916570
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220811	MGI			PMID:34388164
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200716	MGI			PMID:31916570
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220811	MGI			PMID:34388164
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200716	MGI			PMID:31916570
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220811	MGI			PMID:34388164
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:34388164
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:34388164
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20200716	MGI			PMID:31916570
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20220811	MGI			PMID:34388164
1320316	Tesmin	testis expressed metallothionein like	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220811	MGI			PMID:34388164
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:19202056
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:19202056
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:9688956
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9688956
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19202056
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20181108	MGI			PMID:760211
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9688956
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19202056
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0002940	variable body spotting		IEA		N	RGD:5509061	20111116	MGI			
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0005175	non-pigmented tail tip		IAGP		N	RGD:5509061	20141003	MGI			PMID:19202056
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:9475748
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0008779	abnormal maternal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19202056
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0009557	decreased platelet ADP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9475748
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0014168	abnormal brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:9475748
1320319	Dock7	dedicator of cytokinesis 7	gene	MP:0030930	decreased digit pigmentation		IAGP		N	RGD:5509061	20190117	MGI			PMID:19202056
1320320	Sh2d7	SH2 domain containing 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1320321	Klhdc10	kelch domain containing 10	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1320321	Klhdc10	kelch domain containing 10	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1320321	Klhdc10	kelch domain containing 10	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20211014	MGI			PMID:27631783
1320321	Klhdc10	kelch domain containing 10	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1320321	Klhdc10	kelch domain containing 10	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1320321	Klhdc10	kelch domain containing 10	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20211014	MGI			PMID:27631783
1320321	Klhdc10	kelch domain containing 10	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20211014	MGI			PMID:27631783
1320321	Klhdc10	kelch domain containing 10	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20211014	MGI			PMID:27631783
1320326	Dmrta1	doublesex and mab-3 related transcription factor like family A1	gene	MP:0001375	abnormal mating preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982677
1320326	Dmrta1	doublesex and mab-3 related transcription factor like family A1	gene	MP:0009433	polyovular ovarian follicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982677
1320326	Dmrta1	doublesex and mab-3 related transcription factor like family A1	gene	MP:0031629	abnormal mounting behavior		IAGP		N	RGD:5509061	20240704	MGI			PMID:16982677
1320328	Hoxd12	homeobox D12	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1320328	Hoxd12	homeobox D12	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1320328	Hoxd12	homeobox D12	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1320328	Hoxd12	homeobox D12	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1320328	Hoxd12	homeobox D12	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1320328	Hoxd12	homeobox D12	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1320328	Hoxd12	homeobox D12	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1320328	Hoxd12	homeobox D12	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1320328	Hoxd12	homeobox D12	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1320328	Hoxd12	homeobox D12	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1320328	Hoxd12	homeobox D12	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1320328	Hoxd12	homeobox D12	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1320328	Hoxd12	homeobox D12	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1320328	Hoxd12	homeobox D12	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9659925
1320328	Hoxd12	homeobox D12	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8620844
1320328	Hoxd12	homeobox D12	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1320328	Hoxd12	homeobox D12	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521905
1320328	Hoxd12	homeobox D12	gene	MP:0006253	clinodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19108020
1320328	Hoxd12	homeobox D12	gene	MP:0009055	abnormal internal anal sphincter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8787740
1320328	Hoxd12	homeobox D12	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:19108020
1320329	Apol10b	apolipoprotein L 10B	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20210128	MGI			
1320331	Hdac1	histone deacetylase 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0000384	distorted hair follicle pattern		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0001267	enlarged chest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0001282	short vibrissae		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1320331	Hdac1	histone deacetylase 1	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1320331	Hdac1	histone deacetylase 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032080
1320331	Hdac1	histone deacetylase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1320331	Hdac1	histone deacetylase 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0002015	epithelioid cyst		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1320331	Hdac1	histone deacetylase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1320331	Hdac1	histone deacetylase 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1320331	Hdac1	histone deacetylase 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0003929	decreased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
1320331	Hdac1	histone deacetylase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032080
1320331	Hdac1	histone deacetylase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1320331	Hdac1	histone deacetylase 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0004027	trisomy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20260402	MGI			
1320331	Hdac1	histone deacetylase 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1320331	Hdac1	histone deacetylase 1	gene	MP:0005573	increased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1320331	Hdac1	histone deacetylase 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23287868
1320331	Hdac1	histone deacetylase 1	gene	MP:0009598	thin epidermis stratum granulosum		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0010037	ectopic melanocytes		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0010683	dilated hair follicle infundibulum		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1320331	Hdac1	histone deacetylase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19099580
1320331	Hdac1	histone deacetylase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639084
1320331	Hdac1	histone deacetylase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032080
1320331	Hdac1	histone deacetylase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320331	Hdac1	histone deacetylase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032080
1320331	Hdac1	histone deacetylase 1	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20571512
1320331	Hdac1	histone deacetylase 1	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032080
1320331	Hdac1	histone deacetylase 1	gene	MP:0012404	abnormal nail color		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0012405	abnormal nail matrix morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:20194438
1320331	Hdac1	histone deacetylase 1	gene	MP:0013740	Meibomian gland hyperplasia		IAGP		N	RGD:5509061	20150416	MGI			PMID:23792463
1320331	Hdac1	histone deacetylase 1	gene	MP:0030038	abnormal periorbital region morphology		IAGP		N	RGD:5509061	20170914	MGI			PMID:23792463
1320333	Eif4enif1	eukaryotic translation initiation factor 4E nuclear import factor 1	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20181227	MGI			
1320333	Eif4enif1	eukaryotic translation initiation factor 4E nuclear import factor 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20181227	MGI			
1320333	Eif4enif1	eukaryotic translation initiation factor 4E nuclear import factor 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1320333	Eif4enif1	eukaryotic translation initiation factor 4E nuclear import factor 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1320333	Eif4enif1	eukaryotic translation initiation factor 4E nuclear import factor 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20230601	MGI			
1320333	Eif4enif1	eukaryotic translation initiation factor 4E nuclear import factor 1	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20201231	MGI			
1320333	Eif4enif1	eukaryotic translation initiation factor 4E nuclear import factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1320333	Eif4enif1	eukaryotic translation initiation factor 4E nuclear import factor 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20181227	MGI			
1320335	Exo5	exonuclease 5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210729	MGI			PMID:33164760
1320336	Cimap1b	ciliary microtubule associated protein 1B	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20231207	MGI			
1320336	Cimap1b	ciliary microtubule associated protein 1B	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20231207	MGI			
1320336	Cimap1b	ciliary microtubule associated protein 1B	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20231207	MGI			
1320336	Cimap1b	ciliary microtubule associated protein 1B	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20231207	MGI			
1320336	Cimap1b	ciliary microtubule associated protein 1B	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20231207	MGI			
1320336	Cimap1b	ciliary microtubule associated protein 1B	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20231207	MGI			
1320336	Cimap1b	ciliary microtubule associated protein 1B	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20231207	MGI			
1320336	Cimap1b	ciliary microtubule associated protein 1B	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20231207	MGI			
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0005662	increased circulating adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0005665	increased circulating noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178975
1320338	Rnls	renalase, FAD-dependent amine oxidase	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1320340	Anln	anillin, actin binding protein	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20191003	MGI			PMID:30672734
1320340	Anln	anillin, actin binding protein	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20241010	MGI			
1320340	Anln	anillin, actin binding protein	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241010	MGI			
1320340	Anln	anillin, actin binding protein	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20191003	MGI			PMID:30672734
1320340	Anln	anillin, actin binding protein	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1320340	Anln	anillin, actin binding protein	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1320340	Anln	anillin, actin binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1320340	Anln	anillin, actin binding protein	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20250508	MGI			
1320340	Anln	anillin, actin binding protein	gene	MP:0012674	tomacula		IAGP		N	RGD:5509061	20191003	MGI			PMID:30672734
1320344	Fam13a	family with sequence similarity 13, member A	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20191031	MGI			PMID:29386390
1320344	Fam13a	family with sequence similarity 13, member A	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180920	MGI			PMID:26862784
1320344	Fam13a	family with sequence similarity 13, member A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20191031	MGI			PMID:29386390
1320344	Fam13a	family with sequence similarity 13, member A	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20191031	MGI			PMID:29386390
1320344	Fam13a	family with sequence similarity 13, member A	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20191031	MGI			PMID:29386390
1320344	Fam13a	family with sequence similarity 13, member A	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20191031	MGI			PMID:29386390
1320344	Fam13a	family with sequence similarity 13, member A	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20191031	MGI			PMID:29386390
1320344	Fam13a	family with sequence similarity 13, member A	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:29386390
1320345	Apol7c	apolipoprotein L 7c	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39485861
1320345	Apol7c	apolipoprotein L 7c	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20250605	MGI			PMID:39485861
1320350	Ptpn20	protein tyrosine phosphatase, non-receptor type 20	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1320350	Ptpn20	protein tyrosine phosphatase, non-receptor type 20	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20170105	MGI			
1320350	Ptpn20	protein tyrosine phosphatase, non-receptor type 20	gene	MP:0001893	non-obstructive hydrocephaly		IAGP		N	RGD:5509061	20220714	MGI			PMID:35658898
1320350	Ptpn20	protein tyrosine phosphatase, non-receptor type 20	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20230601	MGI			
1320350	Ptpn20	protein tyrosine phosphatase, non-receptor type 20	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20220714	MGI			PMID:35658898
1320350	Ptpn20	protein tyrosine phosphatase, non-receptor type 20	gene	MP:0021024	abnormal cerebrospinal fluid physiology		IAGP		N	RGD:5509061	20220714	MGI			PMID:35658898
1320352	Sla2	Src-like-adaptor 2	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20210128	MGI			
1320352	Sla2	Src-like-adaptor 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20210520	MGI			
1320352	Sla2	Src-like-adaptor 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1320352	Sla2	Src-like-adaptor 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1320352	Sla2	Src-like-adaptor 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220694
1320352	Sla2	Src-like-adaptor 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1320352	Sla2	Src-like-adaptor 2	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1320352	Sla2	Src-like-adaptor 2	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20220519	MGI			
1320352	Sla2	Src-like-adaptor 2	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220694
1320352	Sla2	Src-like-adaptor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220694
1320352	Sla2	Src-like-adaptor 2	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220694
1320352	Sla2	Src-like-adaptor 2	gene	MP:0009455	enhanced cued conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
1320355	Zfp84	zinc finger protein 84	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1320355	Zfp84	zinc finger protein 84	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1320355	Zfp84	zinc finger protein 84	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1320355	Zfp84	zinc finger protein 84	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210520	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20201022	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20210128	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220811	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20180726	MGI			PMID:29784826
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20201022	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20201022	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20180726	MGI			PMID:29784826
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20210520	MGI			
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20180726	MGI			PMID:29784826
1320356	Lrrtm2	leucine rich repeat transmembrane neuronal 2	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20180726	MGI			PMID:29784826
1320358	Tmem11	transmembrane protein 11	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1320358	Tmem11	transmembrane protein 11	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20240307	MGI			PMID:37286744
1320358	Tmem11	transmembrane protein 11	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20240307	MGI			PMID:37286744
1320358	Tmem11	transmembrane protein 11	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20240307	MGI			PMID:37286744
1320358	Tmem11	transmembrane protein 11	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1320358	Tmem11	transmembrane protein 11	gene	MP:0006321	increased myocardial fiber number		IAGP		N	RGD:5509061	20240307	MGI			PMID:37286744
1320358	Tmem11	transmembrane protein 11	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210520	MGI			
1320358	Tmem11	transmembrane protein 11	gene	MP:0031216	decreased susceptibility to myocardial ischemic injury		IAGP		N	RGD:5509061	20240307	MGI			PMID:37286744
1320360	Ndufa6	NADH:ubiquinone oxidoreductase subunit A6	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20220519	MGI			
1320360	Ndufa6	NADH:ubiquinone oxidoreductase subunit A6	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20221215	MGI			
1320360	Ndufa6	NADH:ubiquinone oxidoreductase subunit A6	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20221215	MGI			
1320360	Ndufa6	NADH:ubiquinone oxidoreductase subunit A6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320360	Ndufa6	NADH:ubiquinone oxidoreductase subunit A6	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210729	MGI			PMID:33631794
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20210729	MGI			PMID:33631794
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:28589937
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20210729	MGI			PMID:33631794
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20210729	MGI			PMID:33631794
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20210729	MGI			PMID:33631794
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20210729	MGI			PMID:33631794
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20210729	MGI			PMID:33631794
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0014065	Lewy bodies		IAGP		N	RGD:5509061	20210729	MGI			PMID:33631794
1320362	Chchd2	coiled-coil-helix-coiled-coil-helix domain containing 2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20210729	MGI			PMID:33631794
1320363	Tbc1d12	TBC1D12: TBC1 domain family, member 12	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20241121	MGI			
1320365	Myorg	myogenesis regulating glycosidase (putative)	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1320365	Myorg	myogenesis regulating glycosidase (putative)	gene	MP:0030014	calcified brain		IAGP		N	RGD:5509061	20241226	MGI			PMID:29910000
1320370	Tecta	tectorin alpha	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15995703
1320370	Tecta	tectorin alpha	gene	MP:0002895	abnormal otolithic membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0003143	enlarged otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0003144	decreased otolith number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15995703
1320370	Tecta	tectorin alpha	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0003150	detached tectorial membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0003150	detached tectorial membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:15995703
1320370	Tecta	tectorin alpha	gene	MP:0003150	detached tectorial membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0004412	abnormal cochlear microphonics		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0004412	abnormal cochlear microphonics		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0004414	decreased cochlear microphonics		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0004417	decreased cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:14523068
1320370	Tecta	tectorin alpha	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0006336	abnormal otoacoustic response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0013961	abnormal Hensen stripe morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0013962	absent Hensen stripe		IAGP		N	RGD:5509061	20160310	MGI			PMID:15995703
1320370	Tecta	tectorin alpha	gene	MP:0014088	abnormal Kimura membrane morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:15995703
1320370	Tecta	tectorin alpha	gene	MP:0014088	abnormal Kimura membrane morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:20142329
1320370	Tecta	tectorin alpha	gene	MP:0014088	abnormal Kimura membrane morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0014089	abnormal tectorial membrane marginal band morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:15995703
1320370	Tecta	tectorin alpha	gene	MP:0014089	abnormal tectorial membrane marginal band morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0014090	abnormal tectorial membrane covernet morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0014091	abnormal tectorial membrane striated-sheet matrix morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:11087000
1320370	Tecta	tectorin alpha	gene	MP:0014091	abnormal tectorial membrane striated-sheet matrix morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:15995703
1320370	Tecta	tectorin alpha	gene	MP:0014091	abnormal tectorial membrane striated-sheet matrix morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:24363064
1320370	Tecta	tectorin alpha	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20240405	MGI			PMID:14523068
1320376	Hoxa10	homeobox A10	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0000664	small prostate gland anterior lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915571
1320376	Hoxa10	homeobox A10	gene	MP:0000665	decreased ductal branching in the coagulating gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915571
1320376	Hoxa10	homeobox A10	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915571
1320376	Hoxa10	homeobox A10	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0002670	absent scrotum		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915571
1320376	Hoxa10	homeobox A10	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320376	Hoxa10	homeobox A10	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320376	Hoxa10	homeobox A10	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320376	Hoxa10	homeobox A10	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0003550	short perineum		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0003856	abnormal hindlimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0004651	increased thoracic vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0004654	absent lumbar vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0004680	small xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0004694	absent patella		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1320376	Hoxa10	homeobox A10	gene	MP:0005149	abnormal gubernaculum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0005149	abnormal gubernaculum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7700356
1320376	Hoxa10	homeobox A10	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0009213	absent male inguinal canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0009218	absent peritoneal vaginal process		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1320376	Hoxa10	homeobox A10	gene	MP:0012283	decreased sternebra number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0013317	abnormal seminal vesicle development		IAGP		N	RGD:5509061	20141204	MGI			PMID:9915571
1320376	Hoxa10	homeobox A10	gene	MP:0031286	unilateral cryptorchism		IAGP		N	RGD:5509061	20211014	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0031287	bilateral cryptorchism		IAGP		N	RGD:5509061	20211014	MGI			PMID:7667266
1320376	Hoxa10	homeobox A10	gene	MP:0031287	bilateral cryptorchism		IAGP		N	RGD:5509061	20211014	MGI			PMID:7700356
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080989
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20241121	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080989
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483626
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483626
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080989
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20241121	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483626
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20241121	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080989
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0003285	gastric hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483626
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0003307	pyloric stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483626
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483626
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20241121	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20241121	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080989
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0006001	abnormal intestinal transit time		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483626
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1320378	Irag1	inositol 1,4,5-triphosphate receptor associated 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20241121	MGI			
1320380	Ndufaf5	NADH:ubiquinone oxidoreductase complex assembly factor 5	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20241121	MGI			
1320380	Ndufaf5	NADH:ubiquinone oxidoreductase complex assembly factor 5	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1320380	Ndufaf5	NADH:ubiquinone oxidoreductase complex assembly factor 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1320380	Ndufaf5	NADH:ubiquinone oxidoreductase complex assembly factor 5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20241121	MGI			
1320382	Limd1	LIM domains containing 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092936
1320382	Limd1	LIM domains containing 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092936
1320382	Limd1	LIM domains containing 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1320382	Limd1	LIM domains containing 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1320382	Limd1	LIM domains containing 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1320382	Limd1	LIM domains containing 1	gene	MP:0004983	abnormal osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17092936
1320382	Limd1	LIM domains containing 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1320382	Limd1	LIM domains containing 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1320382	Limd1	LIM domains containing 1	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20250508	MGI			
1320390	Irx5	Iroquois homeobox 5	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0000282	abnormal interatrial septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16182275
1320390	Irx5	Iroquois homeobox 5	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:16182275
1320390	Irx5	Iroquois homeobox 5	gene	MP:0006075	abnormal retina cone bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16182275
1320390	Irx5	Iroquois homeobox 5	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320390	Irx5	Iroquois homeobox 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992950
1320393	Med21	mediator complex subunit 21	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500093
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:8649378
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981960
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10891501
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10891501
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8649378
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8649378
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8649378
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10891501
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10891501
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:10891501
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981960
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10891501
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:8649378
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981960
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11503960
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981960
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0003279	aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0004112	abnormal arteriole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0004125	abnormal venule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0005412	vascular stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10891501
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733157
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11503960
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641300
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0009022	abnormal brain meninges morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981960
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20228226
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10891501
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981960
1320395	Fli1	Fli1 proto-oncogene, ETS transcription factor	gene	MP:0020326	dilated capillary		IAGP		N	RGD:5509061	20160714	MGI			PMID:20228226
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20180524	MGI			PMID:29257953
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20180524	MGI			PMID:29257953
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20180524	MGI			PMID:29257953
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180524	MGI			PMID:29257953
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20180524	MGI			PMID:29257953
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220616	MGI			PMID:29733335
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220616	MGI			PMID:29733335
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20220616	MGI			PMID:29733335
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20180524	MGI			PMID:29257953
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20210128	MGI			
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20220616	MGI			PMID:29733335
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220616	MGI			PMID:29733335
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20180524	MGI			PMID:29257953
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20180524	MGI			PMID:29257953
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20210128	MGI			
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220616	MGI			PMID:29733335
1320398	Enkur	enkurin, TRPC channel interacting protein	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220616	MGI			PMID:29733335
1320400	Fgd2	FYVE, RhoGEF and PH domain containing 2	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17234881
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20181004	MGI			PMID:29859094
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0001599	abnormal blood volume		IAGP		N	RGD:5509061	20170803	MGI			PMID:28559417
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20170803	MGI			PMID:28559417
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20181004	MGI			PMID:29859094
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20170525	MGI			PMID:28077724
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20170803	MGI			PMID:28559417
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20170525	MGI			PMID:28077724
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:29859094
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20170803	MGI			PMID:28559417
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20170803	MGI			PMID:28559417
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20170803	MGI			PMID:28559417
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951310
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951310
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951310
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0010170	abnormal glial cell apoptosis		IAGP		N	RGD:5509061	20170525	MGI			PMID:28077724
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0011080	increased macrophage apoptosis		IAGP		N	RGD:5509061	20170803	MGI			PMID:28559417
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0011986	decreased macrophage proliferation		IAGP		N	RGD:5509061	20170803	MGI			PMID:28559417
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0013662	decreased myeloid cell number		IAGP		N	RGD:5509061	20181004	MGI			PMID:29859094
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0014815	decreased brain gluscose metabolism		IAGP		N	RGD:5509061	20260611	MGI			PMID:28559417
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0020449	decreased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:28077724
1320402	Trem2	triggering receptor expressed on myeloid cells 2	gene	MP:0020449	decreased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:28559417
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200402	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20181227	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20210520	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20181227	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20181227	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0004134	abnormal chest morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0011175	platyspondylia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17952091
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20181227	MGI			
1320405	Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1	gene	MP:0030848	short ilium		IAGP		N	RGD:5509061	20181025	MGI			PMID:17952091
1320407	Pde6c	phosphodiesterase 6C, cGMP specific, cone, alpha prime	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887631
1320407	Pde6c	phosphodiesterase 6C, cGMP specific, cone, alpha prime	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11853768
1320407	Pde6c	phosphodiesterase 6C, cGMP specific, cone, alpha prime	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723493
1320407	Pde6c	phosphodiesterase 6C, cGMP specific, cone, alpha prime	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723493
1320407	Pde6c	phosphodiesterase 6C, cGMP specific, cone, alpha prime	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11853768
1320407	Pde6c	phosphodiesterase 6C, cGMP specific, cone, alpha prime	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887631
1320407	Pde6c	phosphodiesterase 6C, cGMP specific, cone, alpha prime	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11853768
1320407	Pde6c	phosphodiesterase 6C, cGMP specific, cone, alpha prime	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887631
1320411	Rassf10	Ras association (RalGDS/AF-6) domain family (N-terminal) member 10	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20250508	MGI			
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000103	nasal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0000962	disorganized dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0003735	cup-shaped ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004282	retrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004383	absent interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004419	absent parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004475	palatine bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004570	absent glossopharyngeal nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0004873	absent turbinates		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0006211	small orbits		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0009843	decreased neural crest cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0012523	abnormal upper lip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938878
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0013267	first pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0013351	abnormal Rathke's pouch development		IAGP		N	RGD:5509061	20141218	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0030060	absent nasal pit		IAGP		N	RGD:5509061	20170921	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0030084	tympanic ring hypoplasia		IAGP		N	RGD:5509061	20170928	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0030124	middle ear ossicle hypoplasia		IAGP		N	RGD:5509061	20171005	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0030250	frontonasal prominence hypoplasia		IAGP		N	RGD:5509061	20171019	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0030377	zygomatic arch hypoplasia		IAGP		N	RGD:5509061	20171207	MGI			PMID:10888597
1320416	Tcof1	treacle ribosome biogenesis factor 1	gene	MP:0030386	facial bone hypoplasia		IAGP		N	RGD:5509061	20190314	MGI			PMID:15042714
1320417	Zcrb1	zinc finger CCHC-type and RNA binding motif 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1320417	Zcrb1	zinc finger CCHC-type and RNA binding motif 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20241121	MGI			
1320417	Zcrb1	zinc finger CCHC-type and RNA binding motif 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20241121	MGI			
1320417	Zcrb1	zinc finger CCHC-type and RNA binding motif 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1320417	Zcrb1	zinc finger CCHC-type and RNA binding motif 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1320420	Hoxb2	homeobox B2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1320420	Hoxb2	homeobox B2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0000843	absent facial nuclei		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0000843	absent facial nuclei		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1320420	Hoxb2	homeobox B2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197710
1320420	Hoxb2	homeobox B2	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197710
1320420	Hoxb2	homeobox B2	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197710
1320420	Hoxb2	homeobox B2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1320420	Hoxb2	homeobox B2	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1320420	Hoxb2	homeobox B2	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1320420	Hoxb2	homeobox B2	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1320420	Hoxb2	homeobox B2	gene	MP:0004561	absent facial nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1320420	Hoxb2	homeobox B2	gene	MP:0009879	abnormal arcus anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0010892	increased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23197710
1320420	Hoxb2	homeobox B2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1320420	Hoxb2	homeobox B2	gene	MP:0012285	misaligned sternebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0012490	abnormal cochlear VIII nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1320420	Hoxb2	homeobox B2	gene	MP:0012524	abnormal lower lip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0012786	increased rhombomere 1 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0012796	abnormal rhombomere 4 morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0012818	rhombomere transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10230789
1320420	Hoxb2	homeobox B2	gene	MP:0030067	narrow face		IAGP		N	RGD:5509061	20170921	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0030140	facial muscle atrophy		IAGP		N	RGD:5509061	20171214	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0030141	facial paralysis		IAGP		N	RGD:5509061	20171005	MGI			PMID:9012503
1320420	Hoxb2	homeobox B2	gene	MP:0030430	absent levator nasolabialis muscle		IAGP		N	RGD:5509061	20171214	MGI			PMID:9012503
1320423	Tbx18	T-box18	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709898
1320423	Tbx18	T-box18	gene	MP:0000288	abnormal pericardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22926762
1320423	Tbx18	T-box18	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881014
1320423	Tbx18	T-box18	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0000963	fused dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992803
1320423	Tbx18	T-box18	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992803
1320423	Tbx18	T-box18	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153495
1320423	Tbx18	T-box18	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992803
1320423	Tbx18	T-box18	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709898
1320423	Tbx18	T-box18	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22926762
1320423	Tbx18	T-box18	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0003057	abnormal epicardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0003228	abnormal sinus venosus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22926762
1320423	Tbx18	T-box18	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0004134	abnormal chest morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0004682	small intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0004682	small intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0004786	abnormal common cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709898
1320423	Tbx18	T-box18	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992803
1320423	Tbx18	T-box18	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22926762
1320423	Tbx18	T-box18	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20171026	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22926762
1320423	Tbx18	T-box18	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15155583
1320423	Tbx18	T-box18	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24016759
1320423	Tbx18	T-box18	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22926762
1320423	Tbx18	T-box18	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22926762
1320423	Tbx18	T-box18	gene	MP:0011426	abnormal ureter smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20881014
1320423	Tbx18	T-box18	gene	MP:0012496	abnormal pleuropericardial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984617
1320423	Tbx18	T-box18	gene	MP:0031590	abnormal epicardium development		IAGP		N	RGD:5509061	20240229	MGI			PMID:19369973
1320423	Tbx18	T-box18	gene	MP:0031590	abnormal epicardium development		IAGP		N	RGD:5509061	20240229	MGI			PMID:22926762
1320424	Snx19	sorting nexin 19	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1320426	Wdr4	WD repeat domain 4	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20180215	MGI			PMID:26751069
1320426	Wdr4	WD repeat domain 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200917	MGI			PMID:26751069
1320426	Wdr4	WD repeat domain 4	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0008932	abnormal embryonic tissue physiology		IAGP		N	RGD:5509061	20180215	MGI			PMID:26751069
1320426	Wdr4	WD repeat domain 4	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0010962	decreased compact bone mass		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180215	MGI			PMID:26751069
1320426	Wdr4	WD repeat domain 4	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20180215	MGI			PMID:26751069
1320426	Wdr4	WD repeat domain 4	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320426	Wdr4	WD repeat domain 4	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1320428	Ubxn2a	UBX domain protein 2A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221110	MGI			
1320428	Ubxn2a	UBX domain protein 2A	gene	MP:0001785	edema		IEA		N	RGD:5509061	20221110	MGI			
1320428	Ubxn2a	UBX domain protein 2A	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20221110	MGI			
1320428	Ubxn2a	UBX domain protein 2A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320431	Adamdec1	ADAM-like, decysin 1	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20210318	MGI			PMID:27226416
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690440
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690440
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690440
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20200423	MGI			PMID:26392224
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0005285	decreased unsaturated fatty acids level		IAGP		N	RGD:5509061	20200423	MGI			PMID:26392224
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690440
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690440
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200423	MGI			PMID:26392224
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200423	MGI			PMID:26392224
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690440
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690440
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200423	MGI			PMID:26392224
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690440
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0011436	decreased urine magnesium level		IEA		N	RGD:5509061	20211021	MGI			
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0020349	abnormal dendritic cell migration		IAGP		N	RGD:5509061	20200423	MGI			PMID:26392224
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0020950	decreased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:26392224
1320433	Pla2g2d	phospholipase A2, group IID	gene	MP:0031047	decreased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:26392224
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20240523	MGI			
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20240523	MGI			
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20210930	MGI			PMID:34037780
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20210930	MGI			PMID:34037780
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20210930	MGI			PMID:34037780
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20210930	MGI			PMID:34037780
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210930	MGI			PMID:34037780
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210930	MGI			PMID:34037780
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296756
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1320434	Nsrp1	nuclear speckle regulatory protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20240523	MGI			
1320436	Sez6	seizure related gene 6	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170209	MGI			PMID:16814779
1320436	Sez6	seizure related gene 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170209	MGI			PMID:16814779
1320436	Sez6	seizure related gene 6	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20170209	MGI			PMID:16814779
1320436	Sez6	seizure related gene 6	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0003894	abnormal Purkinje cell innervation		IAGP		N	RGD:5509061	20170209	MGI			PMID:16814779
1320436	Sez6	seizure related gene 6	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18031681
1320436	Sez6	seizure related gene 6	gene	MP:0011268	biphasic excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20170209	MGI			PMID:16814779
1320436	Sez6	seizure related gene 6	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20170209	MGI			PMID:16814779
1320436	Sez6	seizure related gene 6	gene	MP:0011272	short excitatory postsynaptic current rise time		IAGP		N	RGD:5509061	20170209	MGI			PMID:16814779
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0008987	abnormal liver lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0009974	decreased cerebral cortex pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0011975	neuronal cytoplasmic inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:23074225
1320442	Ei24	etoposide induced 2.4 mRNA	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:23074225
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20111116	MGI			
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0001136	dilated uterine cervix		IEA		N	RGD:5509061	20111116	MGI			
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0001139	abnormal vagina morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20111116	MGI			
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0002638	abnormal pupillary reflex		IEA		N	RGD:5509061	20111116	MGI			
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0003315	abnormal perineum morphology		IEA		N	RGD:5509061	20111116	MGI			
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0003531	abnormal vagina development		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0003936	abnormal reproductive system development		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0008511	thin retina inner nuclear layer		IEA		N	RGD:5509061	20111116	MGI			
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0009085	abnormal uterine horn morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0009208	abnormal female genitalia morphology		IEA		N	RGD:5509061	20111116	MGI			
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20141003	MGI			
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0013852	abnormal Mullerian duct topology		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320444	Lhfpl2	lipoma HMGIC fusion partner-like 2	gene	MP:0014017	abnormal Wolffian duct connection		IAGP		N	RGD:5509061	20170615	MGI			PMID:26964900
1320445	Spmip7	sperm microtubule inner protein 7	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20210506	MGI			PMID:29700843
1320445	Spmip7	sperm microtubule inner protein 7	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20210506	MGI			PMID:29700843
1320445	Spmip7	sperm microtubule inner protein 7	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:29700843
1320446	Atl3	atlastin GTPase 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1320446	Atl3	atlastin GTPase 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1320446	Atl3	atlastin GTPase 3	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20210520	MGI			
1320446	Atl3	atlastin GTPase 3	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1320446	Atl3	atlastin GTPase 3	gene	MP:0004958	enlarged prostate gland		IEA		N	RGD:5509061	20210520	MGI			
1320446	Atl3	atlastin GTPase 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210520	MGI			
1320451	Rarres2	retinoic acid receptor responder (tazarotene induced) 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22355640
1320451	Rarres2	retinoic acid receptor responder (tazarotene induced) 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22355640
1320451	Rarres2	retinoic acid receptor responder (tazarotene induced) 2	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22355640
1320451	Rarres2	retinoic acid receptor responder (tazarotene induced) 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22355640
1320451	Rarres2	retinoic acid receptor responder (tazarotene induced) 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22355640
1320451	Rarres2	retinoic acid receptor responder (tazarotene induced) 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22355640
1320451	Rarres2	retinoic acid receptor responder (tazarotene induced) 2	gene	MP:0030021	increased muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:22355640
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648486
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648486
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648486
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21390131
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648486
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648486
1320453	Lig3	ligase III, DNA, ATP-dependent	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:21390131
1320457	Maea	macrophage erythroblast attacher	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20160421	MGI			
1320457	Maea	macrophage erythroblast attacher	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16707498
1320457	Maea	macrophage erythroblast attacher	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16707498
1320457	Maea	macrophage erythroblast attacher	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16707498
1320457	Maea	macrophage erythroblast attacher	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16707498
1320457	Maea	macrophage erythroblast attacher	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16707498
1320457	Maea	macrophage erythroblast attacher	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320457	Maea	macrophage erythroblast attacher	gene	MP:0015008	abnormal fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:16707498
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581793
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581793
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581793
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581793
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581793
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581793
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581793
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581793
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:16581793
1320462	Tcea1	transcription elongation factor A (SII) 1	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:16581793
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21695258
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21695258
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22081072
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20181743
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0009641	kidney degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0011435	increased urine magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20181743
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0011707	impaired fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21695258
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21406566
1320467	Mtss1	MTSS I-BAR domain containing 1	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:21695258
1320468	Cep57	centrosomal protein 57	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0004604	abnormal vertebral pedicle morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0005227	abnormal vertebral body development		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320468	Cep57	centrosomal protein 57	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20181108	MGI			PMID:30035751
1320470	Chodl	chondrolectin	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20210520	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0000297	abnormal atrioventricular cushion morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0000520	absent kidney		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0000632	abnormal pineal gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001014	absent superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0002237	abnormal nasal cavity morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0002725	abnormal vein morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0003078	aphakia		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0003327	liver cyst		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0003387	aorta coarctation		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0004055	heart atrium hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0004164	abnormal neurohypophysis morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0004612	fusion of vertebral bodies		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0005105	abnormal middle ear ossicle morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0005262	coloboma		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0006011	abnormal endolymphatic duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0006065	abnormal heart position or orientation		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0008922	abnormal cervical rib		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0009770	abnormal optic chiasm morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0009771	absent optic chiasm		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0010572	persistent right dorsal aorta		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0010647	heart left atrium hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0011493	double ureter		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0011659	interrupted aortic arch, type b		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0012263	decreased hindbrain size		IAGP		N	RGD:5509061	20160630	MGI			PMID:27018474
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013879	duplication of ductus venosus		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013917	persistent right 6th pharyngeal arch artery		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0020486	abnormal lens topology		IEA		N	RGD:5509061	20180628	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1320474	Smg9	SMG9 nonsense mediated mRNA decay factor	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1320477	Arhgef17	Rho guanine nucleotide exchange factor 17	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20221215	MGI			
1320477	Arhgef17	Rho guanine nucleotide exchange factor 17	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20190502	MGI			
1320477	Arhgef17	Rho guanine nucleotide exchange factor 17	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1320479	Brd7	bromodomain containing 7	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1320479	Brd7	bromodomain containing 7	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20141003	MGI			
1320479	Brd7	bromodomain containing 7	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160804	MGI			
1320479	Brd7	bromodomain containing 7	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0001539	decreased caudal vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1320479	Brd7	bromodomain containing 7	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:27444544
1320479	Brd7	bromodomain containing 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20160414	MGI			PMID:25721744
1320479	Brd7	bromodomain containing 7	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0002801	abnormal long-term object recognition memory		IAGP		N	RGD:5509061	20160414	MGI			PMID:25721744
1320479	Brd7	bromodomain containing 7	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20161124	MGI			PMID:27444544
1320479	Brd7	bromodomain containing 7	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20161124	MGI			PMID:27444544
1320479	Brd7	bromodomain containing 7	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1320479	Brd7	bromodomain containing 7	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25721744
1320479	Brd7	bromodomain containing 7	gene	MP:0008821	increased blood uric acid level		IEA		N	RGD:5509061	20160804	MGI			
1320479	Brd7	bromodomain containing 7	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20161124	MGI			PMID:27444544
1320479	Brd7	bromodomain containing 7	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20160414	MGI			PMID:25721744
1320479	Brd7	bromodomain containing 7	gene	MP:0012531	delayed limb development		IAGP		N	RGD:5509061	20161124	MGI			PMID:27444544
1320479	Brd7	bromodomain containing 7	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20210923	MGI			PMID:26878912
1320479	Brd7	bromodomain containing 7	gene	MP:0014365	impaired short-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:25721744
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0000015	abnormal ear pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397220
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0001202	skin photosensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015482
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397220
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015482
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824086
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15939880
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397220
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397220
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015482
1320483	Polh	polymerase (DNA directed), eta (RAD 30 related)	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397220
1320485	Rab6a	RAB6A, member RAS oncogene family	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:26641717
1320485	Rab6a	RAB6A, member RAS oncogene family	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20171116	MGI			PMID:26304202
1320485	Rab6a	RAB6A, member RAS oncogene family	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20171116	MGI			PMID:26641717
1320485	Rab6a	RAB6A, member RAS oncogene family	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:26641717
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20241121	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1320490	Hlcs	holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase)	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1320492	Bdh2	3-hydroxybutyrate dehydrogenase, type 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1320494	Rad23a	RAD23 homolog A, nucleotide excision repair protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12815074
1320494	Rad23a	RAD23 homolog A, nucleotide excision repair protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369441
1320494	Rad23a	RAD23 homolog A, nucleotide excision repair protein	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12815074
1320494	Rad23a	RAD23 homolog A, nucleotide excision repair protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12815074
1320494	Rad23a	RAD23 homolog A, nucleotide excision repair protein	gene	MP:0014762	impaired base-excision repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:12815074
1320496	Dnajc6	DnaJ heat shock protein family (Hsp40) member C6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20160091
1320496	Dnajc6	DnaJ heat shock protein family (Hsp40) member C6	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20160091
1320496	Dnajc6	DnaJ heat shock protein family (Hsp40) member C6	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20160091
1320496	Dnajc6	DnaJ heat shock protein family (Hsp40) member C6	gene	MP:0008976	delayed female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20160091
1320496	Dnajc6	DnaJ heat shock protein family (Hsp40) member C6	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20160091
1320496	Dnajc6	DnaJ heat shock protein family (Hsp40) member C6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20160091
1320497	Rccd1	RCC1 domain containing 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
1320497	Rccd1	RCC1 domain containing 1	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20211021	MGI			
1320500	Arfgef3	ARFGEF family member 3	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20150226	MGI			PMID:24711543
1320500	Arfgef3	ARFGEF family member 3	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24711543
1320500	Arfgef3	ARFGEF family member 3	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20150226	MGI			PMID:24711543
1320500	Arfgef3	ARFGEF family member 3	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20150226	MGI			PMID:24711543
1320500	Arfgef3	ARFGEF family member 3	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:24711543
1320500	Arfgef3	ARFGEF family member 3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20150226	MGI			PMID:24711543
1320500	Arfgef3	ARFGEF family member 3	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20150226	MGI			PMID:24711543
1320500	Arfgef3	ARFGEF family member 3	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20250508	MGI			
1320500	Arfgef3	ARFGEF family member 3	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:24711543
1320502	Prg3	proteoglycan 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1320504	Zfp105	zinc finger protein 105	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20186958
1320504	Zfp105	zinc finger protein 105	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20186958
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19350679
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790473
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15172686
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790473
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19350679
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18470945
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000555	absent carpal bone		IAGP		N	RGD:5509061	20181101	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790473
1320516	Sall1	spalt like transcription factor 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818376
1320516	Sall1	spalt like transcription factor 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15172686
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19350679
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20127799
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19350679
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20127799
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20127799
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003130	anal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790473
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1320516	Sall1	spalt like transcription factor 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818376
1320516	Sall1	spalt like transcription factor 1	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0004637	metacarpal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0004639	fused metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1320516	Sall1	spalt like transcription factor 1	gene	MP:0005034	abnormal anus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790473
1320516	Sall1	spalt like transcription factor 1	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1320516	Sall1	spalt like transcription factor 1	gene	MP:0009052	anal stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790473
1320516	Sall1	spalt like transcription factor 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790473
1320516	Sall1	spalt like transcription factor 1	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0010985	abnormal kidney mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439720
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20127799
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482961
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790473
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818376
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818376
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011363	renal glomerulus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688560
1320516	Sall1	spalt like transcription factor 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915476
1320516	Sall1	spalt like transcription factor 1	gene	MP:0030862	absent triquetrum		IAGP		N	RGD:5509061	20181101	MGI			PMID:12915476
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0004503	decreased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320521	Cops6	COP9 signalosome subunit 6	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317535
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20071779
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0005283	increased unsaturated fatty acids level		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20071779
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0020102	increased hepatic glucose production		IAGP		N	RGD:5509061	20161103	MGI			PMID:26074075
1320526	Ccar2	cell cycle activator and apoptosis regulator 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:20071779
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19657335
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0000726	absent lymphocyte		IAGP		N	RGD:5509061	20141003	MGI			PMID:24591644
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491945
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491945
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24591644
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24591644
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24591644
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491945
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19657335
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491945
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:24591644
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24591644
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24591644
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24591644
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491945
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24591644
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491945
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230003
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717432
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491945
1320528	Bcl11a	BCL11 transcription factor A	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23361909
1320530	Rhobtb2	Rho-related BTB domain containing 2	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1320530	Rhobtb2	Rho-related BTB domain containing 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1320530	Rhobtb2	Rho-related BTB domain containing 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1320530	Rhobtb2	Rho-related BTB domain containing 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20260402	MGI			
1320530	Rhobtb2	Rho-related BTB domain containing 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20260402	MGI			
1320530	Rhobtb2	Rho-related BTB domain containing 2	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20260402	MGI			
1320530	Rhobtb2	Rho-related BTB domain containing 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
1320530	Rhobtb2	Rho-related BTB domain containing 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210520	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20210520	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210520	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210520	MGI			
1320532	Dsg1c	desmoglein 1 gamma	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20170914	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0002999	abnormal bone healing		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0003842	abnormal metopic suture morphology		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0003843	abnormal sagittal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0003843	abnormal sagittal suture morphology		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0004224	absent trabecular meshwork		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0004226	absent Schlemm's canal		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005206	abnormal aqueous humor		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005497	optic nerve cupping		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0006120	mitral valve prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0006219	optic nerve degeneration		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0006249	phthisis bulbi		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0008275	failure of endochondral bone ossification		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0009025	abnormal brain dura mater morphology		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0009303	decreased renal fat pad weight		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0009829	enlarged eye anterior chamber		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0009829	enlarged eye anterior chamber		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0010253	posterior subcapsular cataract		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160310	MGI			PMID:25259869
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20150430	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20230810	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0013732	mature cataract		IAGP		N	RGD:5509061	20190307	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20161027	MGI			PMID:27711054
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0014166	ectopic cranial bone		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0014242	abnormal ribosome biogenesis		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0030030	Wormian bones		IAGP		N	RGD:5509061	20170810	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0030353	wide sagittal suture		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0030439	decreased osteoblast proliferation		IAGP		N	RGD:5509061	20260319	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0030852	abnormal ilium wing morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0030853	abnormal iliac crest morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0030932	hypopyon		IAGP		N	RGD:5509061	20190411	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0030933	hyphema		IAGP		N	RGD:5509061	20190411	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:19669234
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:21282566
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0031500	increased cornea size		IAGP		N	RGD:5509061	20230810	MGI			PMID:20137777
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0031722	abnormal podosome morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:41521804
1320533	Sh3pxd2b	SH3 and PX domains 2B	gene	MP:0031723	abnormal podosome assembly		IAGP		N	RGD:5509061	20260507	MGI			PMID:41521804
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360458
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823927
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823927
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823927
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823927
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360458
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823927
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360458
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823927
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141120	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823927
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360458
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360458
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20171221	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005567	decreased circulating total protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005634	decreased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0005646	abnormal pituitary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360458
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17823927
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0008939	increased pituitary gland weight		IAGP		N	RGD:5509061	20141120	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0009088	thin uterine horn		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0009268	absent cerebellum fissure		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0009342	enlarged gallbladder		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0009362	abnormal primary ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0009370	decreased theca cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974271
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0009957	abnormal cerebellum vermis lobule morphology		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0010280	increased skeletal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19936220
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254685
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0013307	increased adrenal gland weight		IAGP		N	RGD:5509061	20141120	MGI			PMID:18487609
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320535	Wwox	WW domain-containing oxidoreductase	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20231102	MGI			PMID:36828035
1320541	Eya3	EYA transcriptional coactivator and phosphatase 3	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19102749
1320541	Eya3	EYA transcriptional coactivator and phosphatase 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19102749
1320541	Eya3	EYA transcriptional coactivator and phosphatase 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19102749
1320541	Eya3	EYA transcriptional coactivator and phosphatase 3	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19102749
1320541	Eya3	EYA transcriptional coactivator and phosphatase 3	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:19102749
1320541	Eya3	EYA transcriptional coactivator and phosphatase 3	gene	MP:0005586	decreased tidal volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19102749
1320541	Eya3	EYA transcriptional coactivator and phosphatase 3	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19102749
1320541	Eya3	EYA transcriptional coactivator and phosphatase 3	gene	MP:0010394	decreased QRS amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:19102749
1320541	Eya3	EYA transcriptional coactivator and phosphatase 3	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19102749
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0003247	abnormal glutaminergic neuron morphology		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0008431	abnormal short-term spatial reference memory		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320543	Gigyf1	GRB10 interacting GYF protein 1	gene	MP:0021112	impaired social recognition		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1320547	Ly86	lymphocyte antigen 86	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1320547	Ly86	lymphocyte antigen 86	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861286
1320547	Ly86	lymphocyte antigen 86	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861286
1320547	Ly86	lymphocyte antigen 86	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20231207	MGI			
1320547	Ly86	lymphocyte antigen 86	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1320547	Ly86	lymphocyte antigen 86	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1320547	Ly86	lymphocyte antigen 86	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861286
1320547	Ly86	lymphocyte antigen 86	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1320547	Ly86	lymphocyte antigen 86	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1320547	Ly86	lymphocyte antigen 86	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1320547	Ly86	lymphocyte antigen 86	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1320547	Ly86	lymphocyte antigen 86	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20240523	MGI			
1320551	Cactin	cactin, spliceosome C complex subunit	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20240523	MGI			
1320555	Alg2	ALG2 alpha-1,3/1,6-mannosyltransferase	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1320555	Alg2	ALG2 alpha-1,3/1,6-mannosyltransferase	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1320555	Alg2	ALG2 alpha-1,3/1,6-mannosyltransferase	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20240523	MGI			
1320555	Alg2	ALG2 alpha-1,3/1,6-mannosyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1320555	Alg2	ALG2 alpha-1,3/1,6-mannosyltransferase	gene	MP:0011806	decreased dermal fibroblast proliferation		IEA		N	RGD:5509061	20170406	MGI			
1320555	Alg2	ALG2 alpha-1,3/1,6-mannosyltransferase	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1320555	Alg2	ALG2 alpha-1,3/1,6-mannosyltransferase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0003570	increased uterus leiomyoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0009311	increased duodenum adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0009551	increased urinary bladder transitional cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:14695192
1320557	Htatip2	HIV-1 Tat interactive protein 2	gene	MP:0014127	increased thymoma incidence		IAGP		N	RGD:5509061	20160317	MGI			PMID:14695192
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20201022	MGI			
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20181227	MGI			
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0010093	decreased circulating magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692351
1320559	Trpm6	transient receptor potential cation channel, subfamily M, member 6	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20210128	MGI			
1320560	Rnf180	ring finger protein 180	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1320560	Rnf180	ring finger protein 180	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1320560	Rnf180	ring finger protein 180	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20170720	MGI			PMID:23926250
1320560	Rnf180	ring finger protein 180	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20170720	MGI			PMID:23926250
1320560	Rnf180	ring finger protein 180	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1320560	Rnf180	ring finger protein 180	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20170720	MGI			PMID:23926250
1320560	Rnf180	ring finger protein 180	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20170720	MGI			PMID:23926250
1320560	Rnf180	ring finger protein 180	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:23926250
1320560	Rnf180	ring finger protein 180	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20170720	MGI			PMID:23926250
1320560	Rnf180	ring finger protein 180	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20220811	MGI			
1320560	Rnf180	ring finger protein 180	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1320560	Rnf180	ring finger protein 180	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1320560	Rnf180	ring finger protein 180	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20170720	MGI			PMID:23926250
1320560	Rnf180	ring finger protein 180	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20170720	MGI			PMID:23926250
1320560	Rnf180	ring finger protein 180	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20170720	MGI			PMID:23926250
1320561	Mul1	mitochondrial ubiquitin ligase activator of NFKB 1	gene	MP:0005451	abnormal body composition		IAGP		N	RGD:5509061	20230615	MGI			PMID:28273895
1320562	Nsg2	neuron specific gene family member 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1320562	Nsg2	neuron specific gene family member 2	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1320562	Nsg2	neuron specific gene family member 2	gene	MP:0009455	enhanced cued conditioning behavior		IEA		N	RGD:5509061	20230601	MGI			
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316081
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20191219	MGI			PMID:27701636
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17234588
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316081
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447858
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20170720	MGI			PMID:26978024
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0001999	photosensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316081
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:26978024
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20170720	MGI			PMID:26978024
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17234588
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:32620864
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17234588
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17234588
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:27701636
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20170720	MGI			PMID:26978024
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447858
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20191219	MGI			PMID:27701636
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15316081
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0008105	increased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20201105	MGI			PMID:32620864
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0008452	increased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17234588
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915475
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:32620864
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17234588
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0011964	increased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0012671	retina spots		IAGP		N	RGD:5509061	20181220	MGI			PMID:30372741
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0014495	increased circulating chemokine level		IAGP		N	RGD:5509061	20260219	MGI			PMID:35868845
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0014902	increased circulating CCL2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:35868845
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:17234588
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0030006	decreased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:24339791
1320565	Crb1	crumbs family member 1, photoreceptor morphogenesis associated	gene	MP:0031220	increased circulating CXCL10 level		IAGP		N	RGD:5509061	20240404	MGI			PMID:35868845
1320566	Tmem135	transmembrane protein 135	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20250424	MGI			PMID:39970612
1320566	Tmem135	transmembrane protein 135	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0004364	thin stria vascularis		IAGP		N	RGD:5509061	20250424	MGI			PMID:39970612
1320566	Tmem135	transmembrane protein 135	gene	MP:0004396	decreased cochlear inner hair cell number		IAGP		N	RGD:5509061	20250424	MGI			PMID:39970612
1320566	Tmem135	transmembrane protein 135	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20250424	MGI			PMID:39970612
1320566	Tmem135	transmembrane protein 135	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20250424	MGI			PMID:39970612
1320566	Tmem135	transmembrane protein 135	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0005549	retina pigment epithelium hyperplasia		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0006039	decreased mitochondrial fission		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20191114	MGI			PMID:27863209
1320566	Tmem135	transmembrane protein 135	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20250424	MGI			PMID:39970612
1320566	Tmem135	transmembrane protein 135	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20250424	MGI			PMID:39970612
1320566	Tmem135	transmembrane protein 135	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20250424	MGI			PMID:39970612
1320566	Tmem135	transmembrane protein 135	gene	MP:0014740	increased auditory brainstem response wave peak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:39970612
1320566	Tmem135	transmembrane protein 135	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:39970612
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11448938
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11448938
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16291793
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024028
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784500
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16291793
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356169
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11448938
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18940590
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11448938
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0001559	hyperglycemia		IEA		N	RGD:5509061	20111116	MGI			
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0001759	increased urine glucose level		IEA		N	RGD:5509061	20111116	MGI			
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16291793
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11448938
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11448938
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:18940590
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0002659	pituitary gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784500
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11448938
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11448938
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0005331	insulin resistance		IEA		N	RGD:5509061	20111116	MGI			
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16291793
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11448938
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024028
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356169
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17356169
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0006353	increased glycosylated hemoglobin level		IEA		N	RGD:5509061	20111116	MGI			
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0008845	abnormal paraventricular hypothalamic nucleus morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:9784500
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0008846	abnormal supraoptic nucleus morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:9784500
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0009468	absent magnocellular neurosecretory cells		IAGP		N	RGD:5509061	20141204	MGI			PMID:9784500
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14982752
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784500
1320568	Sim1	single-minded family bHLH transcription factor 1	gene	MP:0013340	abnormal pituicyte morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:9784500
1320572	Paox	polyamine oxidase (exo-N4-amino)	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1320572	Paox	polyamine oxidase (exo-N4-amino)	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1320572	Paox	polyamine oxidase (exo-N4-amino)	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1320572	Paox	polyamine oxidase (exo-N4-amino)	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
1320572	Paox	polyamine oxidase (exo-N4-amino)	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1320572	Paox	polyamine oxidase (exo-N4-amino)	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1320572	Paox	polyamine oxidase (exo-N4-amino)	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1320572	Paox	polyamine oxidase (exo-N4-amino)	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1320574	Tgs1	trimethylguanosine synthase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982455
1320574	Tgs1	trimethylguanosine synthase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982455
1320574	Tgs1	trimethylguanosine synthase 1	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982455
1320574	Tgs1	trimethylguanosine synthase 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982455
1320574	Tgs1	trimethylguanosine synthase 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982455
1320574	Tgs1	trimethylguanosine synthase 1	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982455
1320574	Tgs1	trimethylguanosine synthase 1	gene	MP:0008932	abnormal embryonic tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982455
1320574	Tgs1	trimethylguanosine synthase 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982455
1320574	Tgs1	trimethylguanosine synthase 1	gene	MP:0011707	impaired fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22982455
1320586	Arrdc1	arrestin domain containing 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1320586	Arrdc1	arrestin domain containing 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1320586	Arrdc1	arrestin domain containing 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1320586	Arrdc1	arrestin domain containing 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1320586	Arrdc1	arrestin domain containing 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20161208	MGI			PMID:27462458
1320586	Arrdc1	arrestin domain containing 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0009370	decreased theca cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
1320588	Schip1	schwannomin interacting protein 1	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:17143286
1320590	Cbfb	core binding factor beta	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434156
1320590	Cbfb	core binding factor beta	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434156
1320590	Cbfb	core binding factor beta	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9159135
1320590	Cbfb	core binding factor beta	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478528
1320590	Cbfb	core binding factor beta	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901586
1320590	Cbfb	core binding factor beta	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20160128	MGI			PMID:26418744
1320590	Cbfb	core binding factor beta	gene	MP:0000969	abnormal nociceptor morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:26418744
1320590	Cbfb	core binding factor beta	gene	MP:0000972	abnormal mechanoreceptor morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:26418744
1320590	Cbfb	core binding factor beta	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152542
1320590	Cbfb	core binding factor beta	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20200514	MGI			PMID:28819283
1320590	Cbfb	core binding factor beta	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478528
1320590	Cbfb	core binding factor beta	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200514	MGI			PMID:28819283
1320590	Cbfb	core binding factor beta	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901586
1320590	Cbfb	core binding factor beta	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152542
1320590	Cbfb	core binding factor beta	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901586
1320590	Cbfb	core binding factor beta	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9159135
1320590	Cbfb	core binding factor beta	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20160128	MGI			PMID:26418744
1320590	Cbfb	core binding factor beta	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901586
1320590	Cbfb	core binding factor beta	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9159135
1320590	Cbfb	core binding factor beta	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776905
1320590	Cbfb	core binding factor beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160128	MGI			PMID:26418744
1320590	Cbfb	core binding factor beta	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478528
1320590	Cbfb	core binding factor beta	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1320590	Cbfb	core binding factor beta	gene	MP:0002414	abnormal myeloblast morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0002445	abnormal mononuclear cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152542
1320590	Cbfb	core binding factor beta	gene	MP:0002450	abnormal lymph organ development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178013
1320590	Cbfb	core binding factor beta	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434156
1320590	Cbfb	core binding factor beta	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178013
1320590	Cbfb	core binding factor beta	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9159135
1320590	Cbfb	core binding factor beta	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901586
1320590	Cbfb	core binding factor beta	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20160128	MGI			PMID:26418744
1320590	Cbfb	core binding factor beta	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1320590	Cbfb	core binding factor beta	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0004134	abnormal chest morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0004339	absent clavicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0004508	abnormal pectoral girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478528
1320590	Cbfb	core binding factor beta	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1320590	Cbfb	core binding factor beta	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200514	MGI			PMID:28819283
1320590	Cbfb	core binding factor beta	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1320590	Cbfb	core binding factor beta	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1320590	Cbfb	core binding factor beta	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:26418744
1320590	Cbfb	core binding factor beta	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0006051	brainstem hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901586
1320590	Cbfb	core binding factor beta	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9159135
1320590	Cbfb	core binding factor beta	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776905
1320590	Cbfb	core binding factor beta	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1320590	Cbfb	core binding factor beta	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0008077	abnormal CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1320590	Cbfb	core binding factor beta	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1320590	Cbfb	core binding factor beta	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178013
1320590	Cbfb	core binding factor beta	gene	MP:0008253	absent megakaryocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478528
1320590	Cbfb	core binding factor beta	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21178013
1320590	Cbfb	core binding factor beta	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646405
1320590	Cbfb	core binding factor beta	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20221124	MGI			PMID:31171577
1320590	Cbfb	core binding factor beta	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152542
1320590	Cbfb	core binding factor beta	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478528
1320590	Cbfb	core binding factor beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12239155
1320590	Cbfb	core binding factor beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434156
1320590	Cbfb	core binding factor beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940420
1320590	Cbfb	core binding factor beta	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413472
1320590	Cbfb	core binding factor beta	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200514	MGI			PMID:28819283
1320590	Cbfb	core binding factor beta	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152542
1320590	Cbfb	core binding factor beta	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901586
1320590	Cbfb	core binding factor beta	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929537
1320590	Cbfb	core binding factor beta	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9159135
1320590	Cbfb	core binding factor beta	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478528
1320590	Cbfb	core binding factor beta	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20478528
1320590	Cbfb	core binding factor beta	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929538
1320590	Cbfb	core binding factor beta	gene	MP:0011615	submucous cleft palate		IAGP		N	RGD:5509061	20221124	MGI			PMID:31171577
1320590	Cbfb	core binding factor beta	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0011712	arrested osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:12434152
1320590	Cbfb	core binding factor beta	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20200514	MGI			PMID:28819283
1320590	Cbfb	core binding factor beta	gene	MP:0014106	delayed chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:12434155
1320590	Cbfb	core binding factor beta	gene	MP:0014609	abnormal bone marrow cavity size		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320590	Cbfb	core binding factor beta	gene	MP:0021214	anterior cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:31171577
1320590	Cbfb	core binding factor beta	gene	MP:0030273	mandibular retrognathia		IAGP		N	RGD:5509061	20251016	MGI			PMID:24850862
1320594	Tbcb	tubulin folding cofactor B	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1320594	Tbcb	tubulin folding cofactor B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1320594	Tbcb	tubulin folding cofactor B	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0002715	decreased glycogen catabolism rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0005440	increased glycogen level		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0010580	decreased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21856731
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0012051	spasticity		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0014068	abnormal muscle glycogen level		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0014072	decreased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:21075835
1320599	Gbe1	1,4-alpha-glucan branching enzyme 1	gene	MP:0014074	increased brain glycogen level		IAGP		N	RGD:5509061	20160526	MGI			PMID:26385640
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0000168	abnormal bone marrow development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14761685
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20211021	MGI			
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14761685
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160421	MGI			
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14761685
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14761685
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:14761685
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:14761685
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20111116	MGI			
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14761685
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1320602	Gsta4	glutathione S-transferase, alpha 4	gene	MP:0011954	shortened PQ interval		IEA		N	RGD:5509061	20260402	MGI			
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0003663	abnormal thermosensation		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0010055	abnormal sensory neuron physiology		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0020374	abnormal nocifensive behavior		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320603	Slc45a4	solute carrier family 45, member 4	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20250925	MGI			PMID:40836097
1320606	Lpin3	lipin 3	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1320606	Lpin3	lipin 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20220519	MGI			
1320606	Lpin3	lipin 3	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1320606	Lpin3	lipin 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20230601	MGI			
1320606	Lpin3	lipin 3	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20220519	MGI			
1320606	Lpin3	lipin 3	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20220519	MGI			
1320606	Lpin3	lipin 3	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1320606	Lpin3	lipin 3	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20191226	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0014958	decreased lung enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0014966	decreased heart enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0014970	decreased muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0014972	decreased spleen enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1320606	Lpin3	lipin 3	gene	MP:0014975	decreased kidney enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:24634820
1320608	Tlr1	toll-like receptor 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091878
1320608	Tlr1	toll-like receptor 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091878
1320608	Tlr1	toll-like receptor 1	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091878
1320608	Tlr1	toll-like receptor 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077222
1320608	Tlr1	toll-like receptor 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077222
1320608	Tlr1	toll-like receptor 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077222
1320613	Epb41l4b	erythrocyte membrane protein band 4.1 like 4b	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20191010	MGI			PMID:29898395
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20191010	MGI			PMID:29898395
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20191010	MGI			PMID:29898395
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20191010	MGI			PMID:29898395
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20191010	MGI			PMID:29898395
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20191010	MGI			PMID:29898395
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0011275	abnormal behavioral response to light		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320616	Pogz	pogo transposable element with ZNF domain	gene	MP:0020870	decreased thigmotaxis		IAGP		N	RGD:5509061	20240404	MGI			PMID:32103003
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170720	MGI			PMID:27492080
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431235
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20170720	MGI			PMID:27492080
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:27492080
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20170720	MGI			PMID:27492080
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20220519	MGI			
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20200402	MGI			
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis		IAGP		N	RGD:5509061	20170720	MGI			PMID:27492080
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:27492080
1320618	Zscan21	zinc finger and SCAN domain containing 21	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:27492080
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20191128	MGI			
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805751
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805751
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20181227	MGI			
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805751
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320620	Hnrnpc	heterogeneous nuclear ribonucleoprotein C	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320621	Gramd4	GRAM domain containing 4	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20260528	MGI			PMID:38823019
1320621	Gramd4	GRAM domain containing 4	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20260528	MGI			PMID:38823019
1320621	Gramd4	GRAM domain containing 4	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20260528	MGI			PMID:38823019
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1320624	Bltp1	bridge-like lipid transfer protein family member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210826	MGI			
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075009
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075009
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0001922	reduced male fertility		IEA		N	RGD:5509061	20111116	MGI			
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2346121
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0001935	decreased litter size		IEA		N	RGD:5509061	20111116	MGI			
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075009
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075009
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1759685
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2346121
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0008545	absent sperm flagellum		IEA		N	RGD:5509061	20111116	MGI			
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075009
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20250306	MGI			PMID:2346121
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2346121
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2346121
1320627	Hook1	hook microtubule tethering protein 1	gene	MP:0009377	ectopic manchette		IAGP		N	RGD:5509061	20141003	MGI			PMID:2346121
1320629	Sec22b	SEC22 homolog B, vesicle trafficking protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20170914	MGI			PMID:28115522
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20170914	MGI			PMID:28115522
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20170914	MGI			PMID:28115522
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210826	MGI			
1320633	Uhrf2	ubiquitin-like, containing PHD and RING finger domains 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1320635	Podn	podocan	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20220811	MGI			
1320635	Podn	podocan	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1320635	Podn	podocan	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20231207	MGI			
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0001785	edema		IEA		N	RGD:5509061	20231207	MGI			
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20231207	MGI			
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20241121	MGI			
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0008385	absent basisphenoid bone		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0010059	olfactory bulb hypoplasia		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20231207	MGI			
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0012683	absent telencephalon		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0030191	narrow snout		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0030268	agnathia		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320637	Nosip	nitric oxide synthase interacting protein	gene	MP:0030558	absent nasopharynx		IAGP		N	RGD:5509061	20210603	MGI			PMID:25546391
1320642	Washc4	WASH complex subunit 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191128	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191128	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191128	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191128	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0010540	long stride length		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0012319	fast extinction of fear memory		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320642	Washc4	WASH complex subunit 4	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191128	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191128	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1320642	Washc4	WASH complex subunit 4	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:33749590
1320647	Bola2	bolA family member 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1320647	Bola2	bolA family member 2	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1320647	Bola2	bolA family member 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201231	MGI			
1320647	Bola2	bolA family member 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20170105	MGI			
1320647	Bola2	bolA family member 2	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1320647	Bola2	bolA family member 2	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1320647	Bola2	bolA family member 2	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1320647	Bola2	bolA family member 2	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1320647	Bola2	bolA family member 2	gene	MP:0012478	decreased secondary somatosensory cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1320647	Bola2	bolA family member 2	gene	MP:0013909	small third ventricle		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646209
1320651	Cideb	cell death-inducing DNA fragmentation factor, alpha subunit-like effector B	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:17646209
1320653	Hoxa9	homeobox A9	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1320653	Hoxa9	homeobox A9	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761289
1320653	Hoxa9	homeobox A9	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1320653	Hoxa9	homeobox A9	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892669
1320653	Hoxa9	homeobox A9	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761289
1320653	Hoxa9	homeobox A9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761289
1320653	Hoxa9	homeobox A9	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892669
1320653	Hoxa9	homeobox A9	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0003344	mammary gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9892669
1320653	Hoxa9	homeobox A9	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0004323	sternum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013929
1320653	Hoxa9	homeobox A9	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0004614	caudal vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761289
1320653	Hoxa9	homeobox A9	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761289
1320653	Hoxa9	homeobox A9	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8625797
1320653	Hoxa9	homeobox A9	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761289
1320653	Hoxa9	homeobox A9	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320653	Hoxa9	homeobox A9	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1320658	Sbno1	strawberry notch 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1320658	Sbno1	strawberry notch 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20190103	MGI			PMID:28401892
1320658	Sbno1	strawberry notch 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20181227	MGI			
1320658	Sbno1	strawberry notch 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20190103	MGI			PMID:28401892
1320658	Sbno1	strawberry notch 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20181227	MGI			
1320658	Sbno1	strawberry notch 1	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20190103	MGI			PMID:28401892
1320658	Sbno1	strawberry notch 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20190103	MGI			PMID:28401892
1320658	Sbno1	strawberry notch 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1320658	Sbno1	strawberry notch 1	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
1320658	Sbno1	strawberry notch 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20190103	MGI			PMID:28401892
1320658	Sbno1	strawberry notch 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320658	Sbno1	strawberry notch 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320658	Sbno1	strawberry notch 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0000322	increased granulocyte number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20211021	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170105	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20160114	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0008097	increased plasma cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0008126	increased dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0008181	increased marginal zone B cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0008211	decreased mature B cell number		IEA		N	RGD:5509061	20160804	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0008346	increased gamma-delta T cell number		IEA		N	RGD:5509061	20160804	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0008524	increased plasmacytoid dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20211021	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013418	increased memory-marker gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013421	increased CD5-positive gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013430	increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013433	increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013514	increased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013651	increased CD11b-low dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013675	decreased Ly6C-positive mature NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1320659	Dph6	diphthamine biosynthesis 6	gene	MP:0013775	increased KLRG1-positive T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20260402	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20260402	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20260402	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0009263	abnormal eyelid fusion		IEA		N	RGD:5509061	20260402	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0009908	protruding tongue		IEA		N	RGD:5509061	20260402	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1320665	Ppfibp1	PTPRF interacting protein, binding protein 1 (liprin beta 1)	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20260402	MGI			
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0011256	abnormal neural fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0012081	absent heart tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0012086	absent hindgut		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0012183	decreased paraxial mesoderm size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320667	Mixl1	Mix paired-like homeobox	gene	MP:0012739	abnormal anterior primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12117810
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20201231	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20161201	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20170105	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20170105	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20201231	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1320670	Ndufs7	NADH:ubiquinone oxidoreductase core subunit S7	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320673	Cd7	CD7 antigen	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637484
1320673	Cd7	CD7 antigen	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1320673	Cd7	CD7 antigen	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1320673	Cd7	CD7 antigen	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637484
1320673	Cd7	CD7 antigen	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637484
1320673	Cd7	CD7 antigen	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637484
1320677	Arhgap12	Rho GTPase activating protein 12	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1320677	Arhgap12	Rho GTPase activating protein 12	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1320677	Arhgap12	Rho GTPase activating protein 12	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1320679	Ube2h	ubiquitin-conjugating enzyme E2H	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1320682	Gsx1	GS homeobox 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0001746	abnormal pituitary secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0001752	abnormal hypothalamus secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0002163	abnormal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0002164	abnormal gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0003663	abnormal thermosensation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0004103	abnormal ventral striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731457
1320682	Gsx1	GS homeobox 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0006399	abnormal long bone epiphyseal ossification zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0008329	decreased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0008332	decreased lactotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:11731457
1320682	Gsx1	GS homeobox 1	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:8631293
1320682	Gsx1	GS homeobox 1	gene	MP:0014270	decreased ovary secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:8631293
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20230413	MGI			PMID:36271145
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20201015	MGI			PMID:30867229
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20201015	MGI			PMID:30867229
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20230413	MGI			PMID:36271145
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20230413	MGI			PMID:36271145
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20230413	MGI			PMID:36271145
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30867229
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30867229
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0012573	decreased susceptibility to chemically induced skin inflammation		IAGP		N	RGD:5509061	20230413	MGI			PMID:36271145
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20230413	MGI			PMID:36271145
1320684	Cmtm4	CKLF-like MARVEL transmembrane domain containing 4	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20201015	MGI			PMID:30867229
1320686	Ramac	RNA guanine-7 methyltransferase activating subunit	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20241003	MGI			
1320686	Ramac	RNA guanine-7 methyltransferase activating subunit	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20241003	MGI			
1320686	Ramac	RNA guanine-7 methyltransferase activating subunit	gene	MP:0002582	disorganized extraembryonic tissue		IEA		N	RGD:5509061	20241003	MGI			
1320686	Ramac	RNA guanine-7 methyltransferase activating subunit	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241003	MGI			
1320686	Ramac	RNA guanine-7 methyltransferase activating subunit	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1320686	Ramac	RNA guanine-7 methyltransferase activating subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1320686	Ramac	RNA guanine-7 methyltransferase activating subunit	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1320688	Otud6b	OTU domain containing 6B	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1320688	Otud6b	OTU domain containing 6B	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20170525	MGI			PMID:28343629
1320688	Otud6b	OTU domain containing 6B	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20170525	MGI			PMID:28343629
1320688	Otud6b	OTU domain containing 6B	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:28343629
1320688	Otud6b	OTU domain containing 6B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320691	Cstf2t	cleavage stimulation factor, 3' pre-RNA subunit 2, tau	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077340
1320691	Cstf2t	cleavage stimulation factor, 3' pre-RNA subunit 2, tau	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077340
1320691	Cstf2t	cleavage stimulation factor, 3' pre-RNA subunit 2, tau	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077340
1320691	Cstf2t	cleavage stimulation factor, 3' pre-RNA subunit 2, tau	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077340
1320691	Cstf2t	cleavage stimulation factor, 3' pre-RNA subunit 2, tau	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077340
1320691	Cstf2t	cleavage stimulation factor, 3' pre-RNA subunit 2, tau	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077340
1320691	Cstf2t	cleavage stimulation factor, 3' pre-RNA subunit 2, tau	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077340
1320691	Cstf2t	cleavage stimulation factor, 3' pre-RNA subunit 2, tau	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077340
1320691	Cstf2t	cleavage stimulation factor, 3' pre-RNA subunit 2, tau	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:18077340
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1320695	Adh6a	alcohol dehydrogenase 6A (class V)	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20260402	MGI			
1320696	Sptlc3	serine palmitoyltransferase, long chain base subunit 3	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20230119	MGI			
1320696	Sptlc3	serine palmitoyltransferase, long chain base subunit 3	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230119	MGI			
1320696	Sptlc3	serine palmitoyltransferase, long chain base subunit 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1320696	Sptlc3	serine palmitoyltransferase, long chain base subunit 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20250220	MGI			PMID:39661520
1320696	Sptlc3	serine palmitoyltransferase, long chain base subunit 3	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20230119	MGI			
1320696	Sptlc3	serine palmitoyltransferase, long chain base subunit 3	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20250220	MGI			PMID:39661520
1320696	Sptlc3	serine palmitoyltransferase, long chain base subunit 3	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20250220	MGI			PMID:39661520
1320696	Sptlc3	serine palmitoyltransferase, long chain base subunit 3	gene	MP:0020090	decreased susceptibility to diet-induced non-insulin dependent diabetes		IAGP		N	RGD:5509061	20250220	MGI			PMID:39661520
1320696	Sptlc3	serine palmitoyltransferase, long chain base subunit 3	gene	MP:0030973	impaired gluconeogenesis		IAGP		N	RGD:5509061	20250220	MGI			PMID:39661520
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0012204	abnormal neuronal stem cell physiology		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0012207	decreased neuronal stem cell self-renewal		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0020511	decreased dendritic spine length		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0021018	decreased dendritic spine number		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320699	Supt16	SPT16, facilitates chromatin remodeling subunit	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20240425	MGI			PMID:36226587
1320701	Moxd1	monooxygenase, DBH-like 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20201022	MGI			
1320702	Myl6b	myosin, light polypeptide 6B	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1320702	Myl6b	myosin, light polypeptide 6B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1320704	Dnaja4	DnaJ heat shock protein family (Hsp40) member A4	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1320704	Dnaja4	DnaJ heat shock protein family (Hsp40) member A4	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1320704	Dnaja4	DnaJ heat shock protein family (Hsp40) member A4	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1320704	Dnaja4	DnaJ heat shock protein family (Hsp40) member A4	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210520	MGI			
1320704	Dnaja4	DnaJ heat shock protein family (Hsp40) member A4	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20220519	MGI			
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:37000005
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723016
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723016
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723016
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723016
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723016
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0005084	abnormal gallbladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723016
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:37000005
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20231109	MGI			PMID:37000005
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:37000005
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0010414	partial atrioventricular septal defect		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:37000005
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:37000005
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:37000005
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723016
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:37000005
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0030992	atrioventricular cushion hypoplasia		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1320708	Sox7	SRY (sex determining region Y)-box 7	gene	MP:0030992	atrioventricular cushion hypoplasia		IAGP		N	RGD:5509061	20240125	MGI			PMID:37000005
1320712	Npas1	neuronal PAS domain protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1320712	Npas1	neuronal PAS domain protein 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1320712	Npas1	neuronal PAS domain protein 1	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1320712	Npas1	neuronal PAS domain protein 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1320712	Npas1	neuronal PAS domain protein 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1320712	Npas1	neuronal PAS domain protein 1	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1320712	Npas1	neuronal PAS domain protein 1	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1320712	Npas1	neuronal PAS domain protein 1	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15347806
1320714	Foxl2	forkhead box L2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056605
1320714	Foxl2	forkhead box L2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005806
1320714	Foxl2	forkhead box L2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005806
1320714	Foxl2	forkhead box L2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056605
1320714	Foxl2	forkhead box L2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005806
1320714	Foxl2	forkhead box L2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005806
1320714	Foxl2	forkhead box L2	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005806
1320714	Foxl2	forkhead box L2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056605
1320714	Foxl2	forkhead box L2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056605
1320714	Foxl2	forkhead box L2	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056605
1320714	Foxl2	forkhead box L2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005806
1320714	Foxl2	forkhead box L2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20251023	MGI			PMID:40221170
1320714	Foxl2	forkhead box L2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005806
1320714	Foxl2	forkhead box L2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056605
1320714	Foxl2	forkhead box L2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1320714	Foxl2	forkhead box L2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005806
1320714	Foxl2	forkhead box L2	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20220407	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056605
1320714	Foxl2	forkhead box L2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0004853	abnormal ovary size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005806
1320714	Foxl2	forkhead box L2	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15056605
1320714	Foxl2	forkhead box L2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20251023	MGI			PMID:40221170
1320714	Foxl2	forkhead box L2	gene	MP:0011122	absent primordial ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20251023	MGI			PMID:40221170
1320714	Foxl2	forkhead box L2	gene	MP:0013395	eyelid hypoplasia		IAGP		N	RGD:5509061	20141225	MGI			PMID:15056605
1320714	Foxl2	forkhead box L2	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220630	MGI			PMID:23340250
1320714	Foxl2	forkhead box L2	gene	MP:0031018	decreased granulosa cell proliferation		IAGP		N	RGD:5509061	20220407	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:14736745
1320714	Foxl2	forkhead box L2	gene	MP:0031382	absent secondary ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:14736745
1320716	Sprr1a	small proline-rich protein 1A	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20200402	MGI			
1320716	Sprr1a	small proline-rich protein 1A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1320716	Sprr1a	small proline-rich protein 1A	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20201231	MGI			
1320716	Sprr1a	small proline-rich protein 1A	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200402	MGI			
1320719	Itgb3bp	integrin beta 3 binding protein (beta3-endonexin)	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1320719	Itgb3bp	integrin beta 3 binding protein (beta3-endonexin)	gene	MP:0010537	tumor regression		IAGP		N	RGD:5509061	20230622	MGI			PMID:28795467
1320719	Itgb3bp	integrin beta 3 binding protein (beta3-endonexin)	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20230622	MGI			PMID:28795467
1320719	Itgb3bp	integrin beta 3 binding protein (beta3-endonexin)	gene	MP:0013151	abnormal incidence of induced tumors		IAGP		N	RGD:5509061	20230622	MGI			PMID:28795467
1320719	Itgb3bp	integrin beta 3 binding protein (beta3-endonexin)	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:28795467
1320719	Itgb3bp	integrin beta 3 binding protein (beta3-endonexin)	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:28795467
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20181227	MGI			
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20230216	MGI			PMID:31748609
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20200402	MGI			
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220519	MGI			
1320723	Adamts16	ADAM metallopeptidase with thrombospondin type 1 motif 16	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1320725	Calm4	calmodulin 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20220324	MGI			PMID:25316000
1320730	Lpo	lactoperoxidase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20170105	MGI			
1320730	Lpo	lactoperoxidase	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001863	blood vessel inflammation		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0003251	gallbladder inflammation		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0003991	arteriosclerosis		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0010138	arteritis		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0010139	aortitis		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0010152	abnormal brain ependyma morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0010861	increased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0013148	mastitis		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0013485	increased Paneth cell number		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0014221	increased colon goblet cell number		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0014224	increased ileal goblet cell number		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320730	Lpo	lactoperoxidase	gene	MP:0031118	cardiovalvulitis		IAGP		N	RGD:5509061	20220915	MGI			PMID:34127712
1320731	B4galnt4	beta-1,4-N-acetyl-galactosaminyl transferase 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0000466	esophageal epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0003278	esophageal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17137798
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20151210	MGI			PMID:24475238
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213801
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0008090	increased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22547705
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0010945	lung epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851689
1320733	Ndfip1	Nedd4 family interacting protein 1	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20151210	MGI			PMID:24475238
1320739	Eaf1	ELL associated factor 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20201231	MGI			
1320739	Eaf1	ELL associated factor 1	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20220303	MGI			PMID:31229879
1320739	Eaf1	ELL associated factor 1	gene	MP:0003608	prostate gland inflammation		IAGP		N	RGD:5509061	20210506	MGI			PMID:31229879
1320739	Eaf1	ELL associated factor 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20210506	MGI			PMID:31229879
1320739	Eaf1	ELL associated factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320739	Eaf1	ELL associated factor 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1320741	Stx18	syntaxin 18	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1320741	Stx18	syntaxin 18	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320741	Stx18	syntaxin 18	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320741	Stx18	syntaxin 18	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1320743	Cers2	ceramide synthase 2	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801672
1320743	Cers2	ceramide synthase 2	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801672
1320743	Cers2	ceramide synthase 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801672
1320743	Cers2	ceramide synthase 2	gene	MP:0003005	abnormal hippocampal fimbria morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801672
1320743	Cers2	ceramide synthase 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801672
1320743	Cers2	ceramide synthase 2	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801672
1320743	Cers2	ceramide synthase 2	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801672
1320743	Cers2	ceramide synthase 2	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801672
1320745	Myom3	myomesin family, member 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1320745	Myom3	myomesin family, member 3	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1320746	Arglu1	arginine and glutamate rich 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20220519	MGI			
1320746	Arglu1	arginine and glutamate rich 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20191003	MGI			PMID:30698747
1320746	Arglu1	arginine and glutamate rich 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:30698747
1320746	Arglu1	arginine and glutamate rich 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1320746	Arglu1	arginine and glutamate rich 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1320746	Arglu1	arginine and glutamate rich 1	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:30698747
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20111116	MGI			
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230119	MGI			
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114028
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230119	MGI			
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0010166	increased response to stress-induced hyperthermia		IEA		N	RGD:5509061	20111116	MGI			
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114028
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1320748	B4galt5	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230119	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20231207	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20231207	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20240523	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20231207	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20231207	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1320750	Gmps	guanine monophosphate synthetase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20240523	MGI			
1320752	Rbks	ribokinase	gene	MP:0003291	interstinal hyperperistalsis		IAGP		N	RGD:5509061	20201015	MGI			PMID:27194947
1320752	Rbks	ribokinase	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:27194947
1320752	Rbks	ribokinase	gene	MP:0011082	abnormal gastrointestinal motility		IAGP		N	RGD:5509061	20201015	MGI			PMID:27194947
1320754	Cr2	complement receptor 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120817
1320754	Cr2	complement receptor 2	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779753
1320754	Cr2	complement receptor 2	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779753
1320754	Cr2	complement receptor 2	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16082726
1320754	Cr2	complement receptor 2	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779753
1320754	Cr2	complement receptor 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479818
1320754	Cr2	complement receptor 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622941
1320754	Cr2	complement receptor 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779753
1320754	Cr2	complement receptor 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479818
1320754	Cr2	complement receptor 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733878
1320754	Cr2	complement receptor 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622941
1320754	Cr2	complement receptor 2	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479818
1320754	Cr2	complement receptor 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585877
1320754	Cr2	complement receptor 2	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479818
1320754	Cr2	complement receptor 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706534
1320754	Cr2	complement receptor 2	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779753
1320754	Cr2	complement receptor 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733878
1320754	Cr2	complement receptor 2	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067882
1320754	Cr2	complement receptor 2	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706534
1320754	Cr2	complement receptor 2	gene	MP:0004940	abnormal B-1 B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120817
1320754	Cr2	complement receptor 2	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:12165541
1320754	Cr2	complement receptor 2	gene	MP:0008095	abnormal memory B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706534
1320754	Cr2	complement receptor 2	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779753
1320754	Cr2	complement receptor 2	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733878
1320754	Cr2	complement receptor 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371362
1320754	Cr2	complement receptor 2	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371362
1320754	Cr2	complement receptor 2	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733878
1320754	Cr2	complement receptor 2	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706534
1320754	Cr2	complement receptor 2	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779753
1320754	Cr2	complement receptor 2	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479818
1320754	Cr2	complement receptor 2	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479818
1320754	Cr2	complement receptor 2	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479818
1320754	Cr2	complement receptor 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733878
1320754	Cr2	complement receptor 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479818
1320754	Cr2	complement receptor 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733878
1320754	Cr2	complement receptor 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8624815
1320754	Cr2	complement receptor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120817
1320754	Cr2	complement receptor 2	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733878
1320754	Cr2	complement receptor 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11120817
1320754	Cr2	complement receptor 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733878
1320754	Cr2	complement receptor 2	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20190103	MGI			
1320758	Galnt14	polypeptide N-acetylgalactosaminyltransferase 14	gene	MP:0003858	enhanced coordination		IEA		N	RGD:5509061	20170406	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20181227	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20181227	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1320762	Cops7a	COP9 signalosome subunit 7A	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1320764	Rbm39	RNA binding motif protein 39	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20260402	MGI			
1320764	Rbm39	RNA binding motif protein 39	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20250508	MGI			
1320764	Rbm39	RNA binding motif protein 39	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20250508	MGI			
1320764	Rbm39	RNA binding motif protein 39	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20260402	MGI			
1320764	Rbm39	RNA binding motif protein 39	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1320764	Rbm39	RNA binding motif protein 39	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1320764	Rbm39	RNA binding motif protein 39	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20260402	MGI			
1320764	Rbm39	RNA binding motif protein 39	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0003879	abnormal hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0004432	abnormal cochlear hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0011039	abnormal vestibuloocular dark reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320767	Tmc2	transmembrane channel-like gene family 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20181227	MGI			
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20181227	MGI			
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0002607	decreased basophil cell number		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0005628	decreased circulating potassium level		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20181227	MGI			
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0010205	abnormal oligodendrocyte apoptosis		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0011561	renal glomerulus lipidosis		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0011730	increased myelin sheath thickness		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20201112	MGI			PMID:32330411
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0013026	decreased Ly6C low monocyte number		IEA		N	RGD:5509061	20201022	MGI			
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0013138	thin body		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1320769	Pycr2	pyrroline-5-carboxylate reductase family, member 2	gene	MP:0030740	decreased circulating glutamic acid level		IAGP		N	RGD:5509061	20240314	MGI			PMID:33734376
1320771	Vnn1	vanin 1	gene	MP:0014947	abnormal liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:11042271
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0001003	abnormal olfactory receptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728829
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20111116	MGI			
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728829
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17890318
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0002573	behavioral despair		IEA		N	RGD:5509061	20111116	MGI			
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728829
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17890318
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17890318
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17890318
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17890318
1320775	B3gnt2	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728829
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20230914	MGI			PMID:35767949
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587044
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499490
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499490
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724133
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0008552	abnormal circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587044
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20230914	MGI			PMID:35767949
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0020449	decreased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:19587044
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0020943	increased susceptibility to Flaviviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:19587044
1320777	Sarm1	sterile alpha and HEAT/Armadillo motif containing 1	gene	MP:0031044	increased susceptibility to Flaviviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:19587044
1320779	Sema3b	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789413
1320779	Sema3b	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B	gene	MP:0008228	increased anterior commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16202709
1320781	Sdf2l1	stromal cell-derived factor 2-like 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20221208	MGI			
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20141003	MGI			
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0002244	abnormal turbinate morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0006046	atrioventricular valve regurgitation		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20231221	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0006130	pulmonary valve atresia		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0010158	abnormal intestine development		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0010406	common atrium		IEA		N	RGD:5509061	20141003	MGI			
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0010413	complete atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0010460	pulmonary artery hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0011884	absent colon		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0012285	misaligned sternebrae		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0013205	abnormal nonmotile primary cilium morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:25877302
1320782	Cplane1	ciliogenesis and planar polarity effector 1	gene	MP:0031661	prenatal lethality prior to heart atrial septation, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1320792	Fktn	fukutin	gene	MP:0000731	increased collagen deposition in the muscles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1320792	Fktn	fukutin	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1320792	Fktn	fukutin	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1320792	Fktn	fukutin	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1320792	Fktn	fukutin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1320792	Fktn	fukutin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1320792	Fktn	fukutin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1320792	Fktn	fukutin	gene	MP:0003085	abnormal egg cylinder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1320792	Fktn	fukutin	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17034757
1320792	Fktn	fukutin	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017726
1320792	Fktn	fukutin	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017726
1320792	Fktn	fukutin	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1320792	Fktn	fukutin	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1320792	Fktn	fukutin	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1320792	Fktn	fukutin	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1320792	Fktn	fukutin	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1320792	Fktn	fukutin	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1320792	Fktn	fukutin	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1320792	Fktn	fukutin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922256
1320792	Fktn	fukutin	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0011116	absent Reichert's membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0011191	increased embryonic epiblast cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0011201	abnormal visceral yolk sac cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0012094	abnormal Reichert's membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15837576
1320792	Fktn	fukutin	gene	MP:0012185	abnormal muscle precursor cell morphology		IAGP		N	RGD:5509061	20211125	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0012186	abnormal muscle precursor cell physiology		IAGP		N	RGD:5509061	20211125	MGI			PMID:23562821
1320792	Fktn	fukutin	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:23562821
1320795	Cables2	CDK5 and Abl enzyme substrate 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1320795	Cables2	CDK5 and Abl enzyme substrate 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1320795	Cables2	CDK5 and Abl enzyme substrate 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1320795	Cables2	CDK5 and Abl enzyme substrate 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1320795	Cables2	CDK5 and Abl enzyme substrate 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1320795	Cables2	CDK5 and Abl enzyme substrate 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20160616	MGI			PMID:21170031
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:21170031
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20160616	MGI			PMID:21170031
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:21170031
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160616	MGI			PMID:21170031
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20160616	MGI			PMID:21170031
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20190926	MGI			PMID:29695789
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20160616	MGI			PMID:23479606
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20160616	MGI			PMID:23479606
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20160616	MGI			PMID:23479606
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20160616	MGI			PMID:23479606
1320798	Wwp2	WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0030082	long lower incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:21170031
1320800	Dhx58	DExH-box helicase 58	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080593
1320800	Dhx58	DExH-box helicase 58	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080593
1320800	Dhx58	DExH-box helicase 58	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841161
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841161
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008562	increased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080593
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841161
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22841161
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080593
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080593
1320800	Dhx58	DExH-box helicase 58	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1320800	Dhx58	DExH-box helicase 58	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080593
1320800	Dhx58	DExH-box helicase 58	gene	MP:0020912	abnormal susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17475874
1320800	Dhx58	DExH-box helicase 58	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:20080593
1320800	Dhx58	DExH-box helicase 58	gene	MP:0020943	increased susceptibility to Flaviviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:22841161
1320800	Dhx58	DExH-box helicase 58	gene	MP:0031040	increased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:20080593
1320800	Dhx58	DExH-box helicase 58	gene	MP:0031044	increased susceptibility to Flaviviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:22841161
1320800	Dhx58	DExH-box helicase 58	gene	MP:0031704	decreased interferon type I secretion		IAGP		N	RGD:5509061	20260402	MGI			PMID:17475874
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0000648	absent sebaceous gland		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0002074	abnormal hair texture		IEA		N	RGD:5509061	20141003	MGI			
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20141003	MGI			
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20141003	MGI			
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1320804	Arpc4	actin related protein 2/3 complex, subunit 4	gene	MP:0030529	abnormal head skin morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:29113991
1320806	Rnf111	ring finger protein 111	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11298452
1320806	Rnf111	ring finger protein 111	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11298452
1320806	Rnf111	ring finger protein 111	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11298452
1320806	Rnf111	ring finger protein 111	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11298452
1320806	Rnf111	ring finger protein 111	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11298452
1320806	Rnf111	ring finger protein 111	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320806	Rnf111	ring finger protein 111	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20250313	MGI			PMID:38874713
1320808	Tpd52l1	tumor protein D52-like 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1320813	Tor3a	torsin family 3, member A	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1320813	Tor3a	torsin family 3, member A	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1320813	Tor3a	torsin family 3, member A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1320813	Tor3a	torsin family 3, member A	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16945327
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16945327
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16945327
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20201022	MGI			
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16945327
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16945327
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16945327
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16945327
1320815	Hnf4g	hepatocyte nuclear factor 4, gamma	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16945327
1320817	Ttyh1	tweety family member 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568244
1320817	Ttyh1	tweety family member 1	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568244
1320817	Ttyh1	tweety family member 1	gene	MP:0003707	increased cell nucleus count		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568244
1320817	Ttyh1	tweety family member 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568244
1320817	Ttyh1	tweety family member 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568244
1320817	Ttyh1	tweety family member 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1320819	Ddx20	DEAD box helicase 20	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18258677
1320819	Ddx20	DEAD box helicase 20	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20170209	MGI			PMID:18258677
1320819	Ddx20	DEAD box helicase 20	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20170209	MGI			PMID:18258677
1320819	Ddx20	DEAD box helicase 20	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20170209	MGI			PMID:18258677
1320819	Ddx20	DEAD box helicase 20	gene	MP:0004855	increased ovary weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:18258677
1320819	Ddx20	DEAD box helicase 20	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20170209	MGI			PMID:18258677
1320819	Ddx20	DEAD box helicase 20	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:18258677
1320821	Trim27	tripartite motif-containing 27	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
1320821	Trim27	tripartite motif-containing 27	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
1320821	Trim27	tripartite motif-containing 27	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24144979
1320821	Trim27	tripartite motif-containing 27	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
1320821	Trim27	tripartite motif-containing 27	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
1320821	Trim27	tripartite motif-containing 27	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22128329
1320821	Trim27	tripartite motif-containing 27	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22128329
1320821	Trim27	tripartite motif-containing 27	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24144979
1320821	Trim27	tripartite motif-containing 27	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
1320821	Trim27	tripartite motif-containing 27	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22128329
1320821	Trim27	tripartite motif-containing 27	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22128329
1320821	Trim27	tripartite motif-containing 27	gene	MP:0008891	decreased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24144979
1320821	Trim27	tripartite motif-containing 27	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24144979
1320821	Trim27	tripartite motif-containing 27	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24144979
1320821	Trim27	tripartite motif-containing 27	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
1320821	Trim27	tripartite motif-containing 27	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556269
1320825	Armh4	armadillo-like helical domain containing 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1320825	Armh4	armadillo-like helical domain containing 4	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1320825	Armh4	armadillo-like helical domain containing 4	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0002732	increased trichoepithelioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320829	Tnk1	tyrosine kinase, non-receptor, 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974114
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17534888
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210520	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210520	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20220519	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20210128	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17534888
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20210128	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20220519	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0010138	arteritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17534888
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17534888
1320831	Mtap	methylthioadenosine phosphorylase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0001993	abnormal blinking		IAGP		N	RGD:5509061	20170921	MGI			PMID:28114589
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15696194
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0004752	decreased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431181
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15696194
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347711
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347711
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347711
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347711
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347711
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347711
1320833	Tnfrsf14	tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator)	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28114589
1320839	Kctd16	potassium channel tetramerisation domain containing 16	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20180118	MGI			PMID:27717812
1320839	Kctd16	potassium channel tetramerisation domain containing 16	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20180118	MGI			PMID:27717812
1320841	Dpm1	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1320841	Dpm1	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1320841	Dpm1	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1320841	Dpm1	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1320841	Dpm1	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1320841	Dpm1	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1320841	Dpm1	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320841	Dpm1	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0000947	convulsive seizures		IEA		N	RGD:5509061	20170105	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20160421	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20170105	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20160421	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201022	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20160421	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20201022	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
1320842	Tppp	tubulin polymerization promoting protein	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1320844	Pspc1	paraspeckle protein 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1320844	Pspc1	paraspeckle protein 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210826	MGI			
1320844	Pspc1	paraspeckle protein 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210128	MGI			
1320844	Pspc1	paraspeckle protein 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1320844	Pspc1	paraspeckle protein 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1320844	Pspc1	paraspeckle protein 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20190530	MGI			PMID:27809299
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20190530	MGI			PMID:27809299
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20190530	MGI			PMID:27809299
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:27809299
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:27809299
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0012075	impaired mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20190530	MGI			PMID:27809299
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0012765	decreased alpha-beta T cell number		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1320850	Atp6v0a2	ATPase, H+ transporting, lysosomal V0 subunit A2	gene	MP:0013782	abnormal mammary duct terminal end bud morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:27809299
1320852	Tdrd3	tudor domain containing 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1320852	Tdrd3	tudor domain containing 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20150226	MGI			PMID:24507716
1320852	Tdrd3	tudor domain containing 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20150226	MGI			PMID:24507716
1320852	Tdrd3	tudor domain containing 3	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20150226	MGI			PMID:24507716
1320852	Tdrd3	tudor domain containing 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1320854	Med10	mediator complex subunit 10	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1320854	Med10	mediator complex subunit 10	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1320854	Med10	mediator complex subunit 10	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1320854	Med10	mediator complex subunit 10	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1320854	Med10	mediator complex subunit 10	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1320854	Med10	mediator complex subunit 10	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1320854	Med10	mediator complex subunit 10	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1320854	Med10	mediator complex subunit 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320854	Med10	mediator complex subunit 10	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320858	Rinl	Ras and Rab interactor-like	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20240509	MGI			PMID:37703004
1320858	Rinl	Ras and Rab interactor-like	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:37703004
1320858	Rinl	Ras and Rab interactor-like	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:37703004
1320858	Rinl	Ras and Rab interactor-like	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:37703004
1320858	Rinl	Ras and Rab interactor-like	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20240509	MGI			PMID:37703004
1320858	Rinl	Ras and Rab interactor-like	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:37703004
1320858	Rinl	Ras and Rab interactor-like	gene	MP:0010188	abnormal T follicular helper cell differentiation		IAGP		N	RGD:5509061	20240509	MGI			PMID:37703004
1320858	Rinl	Ras and Rab interactor-like	gene	MP:0020912	abnormal susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20240509	MGI			PMID:37703004
1320860	Gtf2e2	general transcription factor II E, polypeptide 2 (beta subunit)	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20201022	MGI			
1320860	Gtf2e2	general transcription factor II E, polypeptide 2 (beta subunit)	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1320860	Gtf2e2	general transcription factor II E, polypeptide 2 (beta subunit)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320860	Gtf2e2	general transcription factor II E, polypeptide 2 (beta subunit)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320860	Gtf2e2	general transcription factor II E, polypeptide 2 (beta subunit)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004325	absent vestibular hair cells		IAGP		N	RGD:5509061	20151001	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004397	absent cochlear inner hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004403	absent cochlear outer hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004405	absent cochlear hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0011060	abnormal kinocilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320862	Tmprss3	transmembrane protease, serine 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21454591
1320864	Nsun7	NOL1/NOP2/Sun domain family, member 7	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442852
1320864	Nsun7	NOL1/NOP2/Sun domain family, member 7	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442852
1320864	Nsun7	NOL1/NOP2/Sun domain family, member 7	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442852
1320864	Nsun7	NOL1/NOP2/Sun domain family, member 7	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:16024820
1320864	Nsun7	NOL1/NOP2/Sun domain family, member 7	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442852
1320864	Nsun7	NOL1/NOP2/Sun domain family, member 7	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442852
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20181227	MGI			PMID:28792939
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20181227	MGI			
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209448
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209448
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20181227	MGI			PMID:28792939
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209448
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209448
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20201022	MGI			
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0010767	abnormal female meiosis I arrest		IAGP		N	RGD:5509061	20181227	MGI			PMID:28792939
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209448
1320866	Tut4	terminal uridylyl transferase 4	gene	MP:0014445	abnormal spindle assembly in female meiosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:28792939
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071760
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000138	absent vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10349618
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10349618
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000461	decreased presacral vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:13575656
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000461	decreased presacral vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000589	thin tail		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835400
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071760
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:13575656
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20809182
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359409
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8436292
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:9383288
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000923	abnormal roof plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533796
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001216	abnormal epidermal layer morphology		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533796
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071760
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:13575656
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001684	abnormal axial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140191
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:1218735
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533796
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835400
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835400
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835400
1320870	T	brachyury, T-box transcription factor T	gene	MP:0001935	decreased litter size		IEA		N	RGD:5509061	20141003	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1003081
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932191
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359409
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8436292
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20150702	MGI			PMID:17247438
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10617567
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:924142
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140191
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002632	vestigial tail		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140191
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13575656
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003047	abnormal thoracic vertebrae morphology		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071760
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20809182
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359409
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140191
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10617567
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:1003081
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:1859671
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:2016041
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:2318411
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359409
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:3422415
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:3653686
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:6722884
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:7461454
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:8690273
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:924142
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20150702	MGI			PMID:17247438
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20150702	MGI			PMID:3678828
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20170817	MGI			PMID:17247632
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20230601	MGI			PMID:28565025
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003861	abnormal nervous system development		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003885	abnormal rostral-caudal body axis extension		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835400
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7207588
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7461454
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20150702	MGI			PMID:17247438
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20150702	MGI			PMID:3678828
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20230601	MGI			PMID:28565025
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533796
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004387	abnormal prechordal plate morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20141003	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004603	absent vertebral arch		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004653	absent caudal vertebrae		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004656	absent sacral vertebrae		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004659	abnormal odontoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004668	absent vertebral body		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004712	notochord degeneration		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004713	split notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004787	abnormal dorsal aorta morphology		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835400
1320870	T	brachyury, T-box transcription factor T	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0005227	abnormal vertebral body development		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0005244	hemopericardium		IEA		N	RGD:5509061	20141003	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0006281	abnormal tail development		IEA		N	RGD:5509061	20141003	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0006392	abnormal nucleus pulposus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:3422415
1320870	T	brachyury, T-box transcription factor T	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:1859671
1320870	T	brachyury, T-box transcription factor T	gene	MP:0008854	bleb		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0008999	absent anus		IEA		N	RGD:5509061	20141003	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0009929	meningomyelocele		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835400
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835400
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1859671
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359409
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9383288
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140191
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10723731
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1218735
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533796
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20809182
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20111208	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0012063	absent tail bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0012063	absent tail bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0012082	delayed heart development		IEA		N	RGD:5509061	20141003	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0012259	meningocele		IAGP		N	RGD:5509061	20200910	MGI			PMID:2658196
1320870	T	brachyury, T-box transcription factor T	gene	MP:0012501	abnormal pericardial cavity morphology		IEA		N	RGD:5509061	20141003	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0012714	decreased ventral ectodermal ridge size		IAGP		N	RGD:5509061	20141003	MGI			PMID:13575656
1320870	T	brachyury, T-box transcription factor T	gene	MP:0012740	abnormal posterior primitive streak morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:8293872
1320870	T	brachyury, T-box transcription factor T	gene	MP:0013164	abnormal forelimb bud morphology		IEA		N	RGD:5509061	20141003	MGI			
1320870	T	brachyury, T-box transcription factor T	gene	MP:0013165	absent forelimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320870	T	brachyury, T-box transcription factor T	gene	MP:0013168	absent hindlimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:5906493
1320876	Tbx19	T-box 19	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20171102	MGI			PMID:12651892
1320876	Tbx19	T-box 19	gene	MP:0000640	adrenal gland hypoplasia		IAGP		N	RGD:5509061	20171102	MGI			PMID:12651892
1320876	Tbx19	T-box 19	gene	MP:0000676	abnormal body water content		IAGP		N	RGD:5509061	20171102	MGI			PMID:12651892
1320876	Tbx19	T-box 19	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20171102	MGI			PMID:12651892
1320876	Tbx19	T-box 19	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20171102	MGI			PMID:12651892
1320876	Tbx19	T-box 19	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20171102	MGI			PMID:12651892
1320876	Tbx19	T-box 19	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20171102	MGI			PMID:12651892
1320876	Tbx19	T-box 19	gene	MP:0008237	abnormal ventral coat pigmentation		IAGP		N	RGD:5509061	20171102	MGI			PMID:12651892
1320876	Tbx19	T-box 19	gene	MP:0008341	decreased corticotroph cell number		IAGP		N	RGD:5509061	20171102	MGI			PMID:12651892
1320878	Kif16b	kinesin family member 16B	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0000495	abnormal colon morphology		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21238925
1320878	Kif16b	kinesin family member 16B	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:21238925
1320878	Kif16b	kinesin family member 16B	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0003271	abnormal duodenum morphology		IEA		N	RGD:5509061	20230119	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1320878	Kif16b	kinesin family member 16B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21238925
1320878	Kif16b	kinesin family member 16B	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21238925
1320878	Kif16b	kinesin family member 16B	gene	MP:0011184	absent embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:21238925
1320879	Tbc1d9b	TBC1 domain family, member 9B	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1320879	Tbc1d9b	TBC1 domain family, member 9B	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1320879	Tbc1d9b	TBC1 domain family, member 9B	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1320879	Tbc1d9b	TBC1 domain family, member 9B	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0003981	decreased circulating phospholipid level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0010331	abnormal apolipoprotein level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0010332	abnormal circulating apolipoprotein level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0020151	abnormal circulating non-HDL cholesterol level		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320880	Ilrun	inflammation and lipid regulator with UBA-like and NBR1-like domains	gene	MP:0020868	decreased lipogenesis		IAGP		N	RGD:5509061	20210311	MGI			PMID:32912065
1320888	Tfr2	transferrin receptor 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0000492	abnormal rectum morphology		IEA		N	RGD:5509061	20210520	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0000495	abnormal colon morphology		IEA		N	RGD:5509061	20210520	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20179178
1320888	Tfr2	transferrin receptor 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20201022	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20179178
1320888	Tfr2	transferrin receptor 2	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20201022	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20179178
1320888	Tfr2	transferrin receptor 2	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12134060
1320888	Tfr2	transferrin receptor 2	gene	MP:0005638	hemochromatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951546
1320888	Tfr2	transferrin receptor 2	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12134060
1320888	Tfr2	transferrin receptor 2	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951546
1320888	Tfr2	transferrin receptor 2	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20179178
1320888	Tfr2	transferrin receptor 2	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12134060
1320888	Tfr2	transferrin receptor 2	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951546
1320888	Tfr2	transferrin receptor 2	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20179178
1320888	Tfr2	transferrin receptor 2	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12134060
1320888	Tfr2	transferrin receptor 2	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951546
1320888	Tfr2	transferrin receptor 2	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20179178
1320888	Tfr2	transferrin receptor 2	gene	MP:0008955	increased cellular hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20179178
1320888	Tfr2	transferrin receptor 2	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20241121	MGI			
1320888	Tfr2	transferrin receptor 2	gene	MP:0011890	increased circulating ferritin level		IEA		N	RGD:5509061	20141003	MGI			
1320891	Ndc80	NDC80 kinetochore complex component	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20240919	MGI			
1320891	Ndc80	NDC80 kinetochore complex component	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20200917	MGI			PMID:32461611
1320891	Ndc80	NDC80 kinetochore complex component	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:32461611
1320891	Ndc80	NDC80 kinetochore complex component	gene	MP:0009769	abnormal meiotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20200917	MGI			PMID:32461611
1320891	Ndc80	NDC80 kinetochore complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1320891	Ndc80	NDC80 kinetochore complex component	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1320891	Ndc80	NDC80 kinetochore complex component	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240919	MGI			
1320893	Jchain	immunoglobulin joining chain	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535625
1320893	Jchain	immunoglobulin joining chain	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535625
1320893	Jchain	immunoglobulin joining chain	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710213
1320893	Jchain	immunoglobulin joining chain	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10395687
1320893	Jchain	immunoglobulin joining chain	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535625
1320893	Jchain	immunoglobulin joining chain	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710213
1320893	Jchain	immunoglobulin joining chain	gene	MP:0001819	abnormal immune cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710213
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10395687
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10395687
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7500036
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002473	impaired complement classical pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710213
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10395687
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535625
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15175647
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7500036
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752925
1320893	Jchain	immunoglobulin joining chain	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710213
1320893	Jchain	immunoglobulin joining chain	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752925
1320893	Jchain	immunoglobulin joining chain	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:7500036
1320893	Jchain	immunoglobulin joining chain	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17056558
1320893	Jchain	immunoglobulin joining chain	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10395687
1320893	Jchain	immunoglobulin joining chain	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9710213
1320893	Jchain	immunoglobulin joining chain	gene	MP:0008864	abnormal intestinal secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7500036
1320893	Jchain	immunoglobulin joining chain	gene	MP:0008864	abnormal intestinal secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752925
1320893	Jchain	immunoglobulin joining chain	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:10814580
1320893	Jchain	immunoglobulin joining chain	gene	MP:0031025	decreased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:10814580
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22327219
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0003865	lymph node inflammation		IAGP		N	RGD:5509061	20200618	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0005535	abnormal body temperature		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529147
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22327219
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22327219
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22327219
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1320897	Ripk1	receptor (TNFRSF)-interacting serine-threonine kinase 1	gene	MP:0031052	lymph node necrosis		IAGP		N	RGD:5509061	20200618	MGI			PMID:9529147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0000935	abnormal folding of telencephalic vesicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0004081	abnormal globus pallidus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20171102	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0004870	small premaxilla		IAGP		N	RGD:5509061	20171102	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136147
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15736266
1320900	Zic5	zinc finger protein of the cerebellum 5	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:15736266
1320903	Liph	lipase H	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857648
1320903	Liph	lipase H	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857648
1320903	Liph	lipase H	gene	MP:0001279	wavy vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857648
1320903	Liph	lipase H	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857648
1320903	Liph	lipase H	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857648
1320903	Liph	lipase H	gene	MP:0003846	matted coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857648
1320903	Liph	lipase H	gene	MP:0008731	abnormal hair shaft melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857648
1320903	Liph	lipase H	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857648
1320905	Srrm2	serine/arginine repetitive matrix 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320907	Ddb2	damage specific DNA binding protein 2	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769931
1320907	Ddb2	damage specific DNA binding protein 2	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16288018
1320907	Ddb2	damage specific DNA binding protein 2	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127714
1320907	Ddb2	damage specific DNA binding protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769931
1320907	Ddb2	damage specific DNA binding protein 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558025
1320907	Ddb2	damage specific DNA binding protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15558025
1320907	Ddb2	damage specific DNA binding protein 2	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16288018
1320907	Ddb2	damage specific DNA binding protein 2	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769931
1320907	Ddb2	damage specific DNA binding protein 2	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14769931
1320912	Eea1	early endosome antigen 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1320912	Eea1	early endosome antigen 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1320912	Eea1	early endosome antigen 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320913	Fermt3	fermitin family member 3	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20160519	MGI			PMID:24969775
1320913	Fermt3	fermitin family member 3	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980064
1320913	Fermt3	fermitin family member 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662549
1320913	Fermt3	fermitin family member 3	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1320913	Fermt3	fermitin family member 3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662549
1320913	Fermt3	fermitin family member 3	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980064
1320913	Fermt3	fermitin family member 3	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980064
1320913	Fermt3	fermitin family member 3	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980064
1320913	Fermt3	fermitin family member 3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23980064
1320913	Fermt3	fermitin family member 3	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662549
1320913	Fermt3	fermitin family member 3	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662549
1320913	Fermt3	fermitin family member 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662549
1320913	Fermt3	fermitin family member 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20160519	MGI			PMID:24969775
1320913	Fermt3	fermitin family member 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662549
1320913	Fermt3	fermitin family member 3	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20160519	MGI			PMID:24969775
1320913	Fermt3	fermitin family member 3	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20160519	MGI			PMID:24969775
1320913	Fermt3	fermitin family member 3	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20160519	MGI			PMID:24969775
1320913	Fermt3	fermitin family member 3	gene	MP:0008816	petechiae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662549
1320913	Fermt3	fermitin family member 3	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160519	MGI			PMID:24969775
1320913	Fermt3	fermitin family member 3	gene	MP:0010177	acanthocytosis		IAGP		N	RGD:5509061	20160519	MGI			PMID:24969775
1320913	Fermt3	fermitin family member 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278053
1320913	Fermt3	fermitin family member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320913	Fermt3	fermitin family member 3	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:24969775
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0006323	abnormal extraembryonic mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0008391	abnormal primordial germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0011187	abnormal parietal endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0011200	abnormal extraembryonic coelom morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23469192
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0011363	renal glomerulus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1320918	Ctdnep1	CTD nuclear envelope phosphatase 1	gene	MP:0011371	decreased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20190502	MGI			
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0009286	increased abdominal fat pad weight		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320924	Gpr61	G protein-coupled receptor 61	gene	MP:0020867	increased lipogenesis		IAGP		N	RGD:5509061	20210318	MGI			PMID:21971119
1320931	Ulk2	unc-51 like kinase 2	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20111116	MGI			
1320931	Ulk2	unc-51 like kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690395
1320931	Ulk2	unc-51 like kinase 2	gene	MP:0010166	increased response to stress-induced hyperthermia		IEA		N	RGD:5509061	20111116	MGI			
1320931	Ulk2	unc-51 like kinase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690395
1320932	Arsk	arylsulfatase K	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20210415	MGI			PMID:32856704
1320932	Arsk	arylsulfatase K	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1320932	Arsk	arylsulfatase K	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20210415	MGI			PMID:32856704
1320932	Arsk	arylsulfatase K	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32856704
1320932	Arsk	arylsulfatase K	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20210415	MGI			PMID:32856704
1320932	Arsk	arylsulfatase K	gene	MP:0011333	abnormal kidney inner medulla morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32856704
1320932	Arsk	arylsulfatase K	gene	MP:0011378	abnormal kidney outer medulla inner stripe morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32856704
1320932	Arsk	arylsulfatase K	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20210415	MGI			PMID:32856704
1320932	Arsk	arylsulfatase K	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:32856704
1320940	Muc19	mucin 19	gene	MP:0004035	abnormal sublingual gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847143
1320940	Muc19	mucin 19	gene	MP:0004035	abnormal sublingual gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23580649
1320940	Muc19	mucin 19	gene	MP:0004035	abnormal sublingual gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3400771
1320940	Muc19	mucin 19	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:8077681
1320940	Muc19	mucin 19	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20150618	MGI			PMID:25447050
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23813972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23813972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20150528	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0002986	decreased urine calcium level		IAGP		N	RGD:5509061	20150528	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20150528	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0003878	abnormal ear physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19586905
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0004292	abnormal spiral ligament fibrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0004427	abnormal vestibular labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19586905
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19586905
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0004814	reduced linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19586905
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23813972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0005544	cornea deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20150528	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19586905
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20150528	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20150528	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0009742	increased cornea stroma thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0011435	increased urine magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0011436	decreased urine magnesium level		IAGP		N	RGD:5509061	20150528	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0011460	decreased urine chloride ion level		IAGP		N	RGD:5509061	20180927	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23813972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20150528	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0020854	increased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0030633	decreased urine creatine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:23942972
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0031178	increased Descemet membrane thickness		IAGP		N	RGD:5509061	20201119	MGI			PMID:20185830
1320942	Slc4a11	solute carrier family 4, sodium bicarbonate transporter-like, member 11	gene	MP:0031178	increased Descemet membrane thickness		IAGP		N	RGD:5509061	20201119	MGI			PMID:23942972
1320944	Dapp1	dual adaptor for phosphotyrosine and 3-phosphoinositides 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14588241
1320944	Dapp1	dual adaptor for phosphotyrosine and 3-phosphoinositides 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563325
1320944	Dapp1	dual adaptor for phosphotyrosine and 3-phosphoinositides 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14588241
1320944	Dapp1	dual adaptor for phosphotyrosine and 3-phosphoinositides 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563325
1320944	Dapp1	dual adaptor for phosphotyrosine and 3-phosphoinositides 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14588241
1320944	Dapp1	dual adaptor for phosphotyrosine and 3-phosphoinositides 1	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563325
1320944	Dapp1	dual adaptor for phosphotyrosine and 3-phosphoinositides 1	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563325
1320944	Dapp1	dual adaptor for phosphotyrosine and 3-phosphoinositides 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563325
1320944	Dapp1	dual adaptor for phosphotyrosine and 3-phosphoinositides 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14588241
1320946	Snx5	sorting nexin 5	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1320946	Snx5	sorting nexin 5	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1320946	Snx5	sorting nexin 5	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1320946	Snx5	sorting nexin 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1320946	Snx5	sorting nexin 5	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1320946	Snx5	sorting nexin 5	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1320946	Snx5	sorting nexin 5	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20160804	MGI			
1320946	Snx5	sorting nexin 5	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0010816	decreased type I pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0010902	abnormal pulmonary alveolar sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320946	Snx5	sorting nexin 5	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23526992
1320951	Snrpb2	U2 small nuclear ribonucleoprotein B	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1320951	Snrpb2	U2 small nuclear ribonucleoprotein B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1320954	Washc1	WASH complex subunit 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974797
1320954	Washc1	WASH complex subunit 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974797
1320954	Washc1	WASH complex subunit 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22718907
1320954	Washc1	WASH complex subunit 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974797
1320954	Washc1	WASH complex subunit 1	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974797
1320954	Washc1	WASH complex subunit 1	gene	MP:0011200	abnormal extraembryonic coelom morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974797
1320954	Washc1	WASH complex subunit 1	gene	MP:0011202	abnormal ectoplacental cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974797
1320954	Washc1	WASH complex subunit 1	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974797
1320956	Slc26a6	solute carrier family 26, member 6	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15574486
1320956	Slc26a6	solute carrier family 26, member 6	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170027
1320956	Slc26a6	solute carrier family 26, member 6	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15574486
1320956	Slc26a6	solute carrier family 26, member 6	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053783
1320956	Slc26a6	solute carrier family 26, member 6	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17053783
1320956	Slc26a6	solute carrier family 26, member 6	gene	MP:0005360	urolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532010
1320956	Slc26a6	solute carrier family 26, member 6	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532010
1320956	Slc26a6	solute carrier family 26, member 6	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532010
1320958	Polr2j	polymerase (RNA) II (DNA directed) polypeptide J	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241017	MGI			
1320958	Polr2j	polymerase (RNA) II (DNA directed) polypeptide J	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241017	MGI			
1320958	Polr2j	polymerase (RNA) II (DNA directed) polypeptide J	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1320958	Polr2j	polymerase (RNA) II (DNA directed) polypeptide J	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1320958	Polr2j	polymerase (RNA) II (DNA directed) polypeptide J	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20241017	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20210826	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210826	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210826	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20210826	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210826	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20240523	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1320960	Ino80c	INO80 complex subunit C	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210826	MGI			
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20220929	MGI			PMID:35127681
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374397
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000155	asymmetric rib joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000422	delayed hair appearance		IEA		N	RGD:5509061	20111116	MGI			
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000449	broad nasal bridge		IAGP		N	RGD:5509061	20220929	MGI			PMID:35127681
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9268572
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374397
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636085
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374397
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636085
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374397
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:35127681
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004339	absent clavicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004422	small temporal bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004441	small occipital bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:35127681
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004459	small alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20171102	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004691	absent pubis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004692	small pubis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20171123	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0006411	upturned snout		IEA		N	RGD:5509061	20111116	MGI			
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0008430	short temporal bone squamous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20220929	MGI			PMID:35127681
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636085
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:35127681
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:35127681
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0010202	focal dorsal hair loss		IEA		N	RGD:5509061	20111116	MGI			
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23979902
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374397
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151126	MGI			PMID:25673119
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636085
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0012528	abnormal zone of polarizing activity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9374397
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030034	depressed nasal bridge		IAGP		N	RGD:5509061	20220929	MGI			PMID:35127681
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030116	bifid nasal tip		IAGP		N	RGD:5509061	20170928	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030117	bifid nose		IAGP		N	RGD:5509061	20170928	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030193	short philtrum		IAGP		N	RGD:5509061	20220929	MGI			PMID:35127681
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030200	abnormal nasal septum cartilage morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:9847249
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030301	abnormal maxillary frontal process morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030384	short facial bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030385	decreased facial bone number		IAGP		N	RGD:5509061	20171207	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030388	large fontanelles		IAGP		N	RGD:5509061	20171207	MGI			PMID:11641221
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0030833	small acromion		IAGP		N	RGD:5509061	20181018	MGI			PMID:15728667
1320964	Alx4	aristaless-like homeobox 4	gene	MP:0031445	midline cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:35127681
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847290
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20230601	MGI			PMID:17807638
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10193444
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5559839
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109702
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:5559839
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5559839
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12485443
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001760	abnormal urine enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:115747
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001942	abnormal lung volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10193444
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:115747
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12009785
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002314	abnormal respiratory mechanics		IAGP		N	RGD:5509061	20141003	MGI			PMID:12009785
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:5559839
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002894	abnormal otolith morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109702
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002894	abnormal otolith morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5559839
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20210520	MGI			
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7089489
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:133823
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12485443
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0004812	abnormal linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109702
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12445206
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20230601	MGI			PMID:17807638
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:5559839
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0006159	ocular albinism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18715234
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0009557	decreased platelet ADP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0010192	abnormal retina melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7089489
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8441253
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:3711636
1320976	Bloc1s6	biogenesis of lysosomal organelles complex-1, subunit 6, pallidin	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:6696991
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0001156	abnormal spermatogenesis		IEA		N	RGD:5509061	20170323	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20170323	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0002687	oligozoospermia		IEA		N	RGD:5509061	20170323	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20201022	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20201022	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201022	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0005578	teratozoospermia		IEA		N	RGD:5509061	20170323	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201022	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320977	Elapor1	endosome-lysosome associated apoptosis and autophagy regulator 1	gene	MP:0011941	increased fluid intake		IEA		N	RGD:5509061	20210128	MGI			
1320979	Ugp2	UDP-glucose pyrophosphorylase 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1320979	Ugp2	UDP-glucose pyrophosphorylase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20190919	MGI			PMID:29604961
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20190919	MGI			PMID:29604961
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20190919	MGI			PMID:29604961
1320983	Orai2	ORAI calcium release-activated calcium modulator 2	gene	MP:0010183	abnormal CD4-positive helper T cell morphology		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1320988	Smtn	smoothelin	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678771
1320988	Smtn	smoothelin	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678771
1320988	Smtn	smoothelin	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20180222	MGI			
1320988	Smtn	smoothelin	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678771
1320988	Smtn	smoothelin	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678771
1320988	Smtn	smoothelin	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678771
1320988	Smtn	smoothelin	gene	MP:0003262	intestinal/bowel diverticulum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678771
1320988	Smtn	smoothelin	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0004006	impaired contractility of jejunal smooth muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0004857	abnormal heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678771
1320988	Smtn	smoothelin	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18678771
1320988	Smtn	smoothelin	gene	MP:0005044	sepsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0006001	abnormal intestinal transit time		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16285958
1320988	Smtn	smoothelin	gene	MP:0011881	distended duodenum		IAGP		N	RGD:5509061	20150702	MGI			PMID:16285958
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:25848754
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20160811	MGI			PMID:25848754
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20160811	MGI			PMID:25848754
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160811	MGI			PMID:25848754
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20160811	MGI			PMID:25848754
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20160811	MGI			PMID:27252784
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0010715	retina coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160811	MGI			PMID:25848754
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160811	MGI			PMID:27252784
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0012091	increased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0012265	increased hindbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0012535	abnormal optic fissure closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0012678	absent fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0013000	absent cerebral aqueduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220025
1320990	Kdm2b	lysine (K)-specific demethylase 2B	gene	MP:0013199	increased head mesenchyme apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:21220025
1320994	Cryzl1	crystallin zeta like 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1320994	Cryzl1	crystallin zeta like 1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20250508	MGI			
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0011585	decreased alkaline phosphatase activity		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320996	Atp6v1h	ATPase, H+ transporting, lysosomal V1 subunit H	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20170330	MGI			PMID:27924156
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999798
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919816
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999798
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20190502	MGI			
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999798
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999798
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077299
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919816
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999798
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077299
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023430
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528298
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919816
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919816
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919816
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528298
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528298
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0008176	abnormal germinal center B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21642988
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21642988
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023430
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409815
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21642988
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528298
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077299
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919816
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8999798
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919816
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919816
1320998	Gna13	guanine nucleotide binding protein, alpha 13	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1321000	Ifrd2	interferon-related developmental regulator 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240627	MGI			PMID:37603466
1321000	Ifrd2	interferon-related developmental regulator 2	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20240627	MGI			PMID:37603466
1321000	Ifrd2	interferon-related developmental regulator 2	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20240627	MGI			PMID:37603466
1321000	Ifrd2	interferon-related developmental regulator 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20240627	MGI			PMID:37603466
1321000	Ifrd2	interferon-related developmental regulator 2	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20240627	MGI			PMID:37603466
1321000	Ifrd2	interferon-related developmental regulator 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20240627	MGI			PMID:37603466
1321000	Ifrd2	interferon-related developmental regulator 2	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20240627	MGI			PMID:37603466
1321000	Ifrd2	interferon-related developmental regulator 2	gene	MP:0011169	abnormal white fat cell differentation		IAGP		N	RGD:5509061	20240627	MGI			PMID:37603466
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0010332	abnormal circulating apolipoprotein level		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20170216	MGI			PMID:25806685
1321001	Lpcat3	lysophosphatidylcholine acyltransferase 3	gene	MP:0021045	decreased circulating VLDL phospholipid level		IAGP		N	RGD:5509061	20220106	MGI			PMID:25806685
1321002	Eci3	enoyl-Coenzyme A delta isomerase 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321006	Frs3	fibroblast growth factor receptor substrate 3	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1321006	Frs3	fibroblast growth factor receptor substrate 3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1321006	Frs3	fibroblast growth factor receptor substrate 3	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1321006	Frs3	fibroblast growth factor receptor substrate 3	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1321006	Frs3	fibroblast growth factor receptor substrate 3	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1321006	Frs3	fibroblast growth factor receptor substrate 3	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1321006	Frs3	fibroblast growth factor receptor substrate 3	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1321006	Frs3	fibroblast growth factor receptor substrate 3	gene	MP:0012683	absent telencephalon		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1321006	Frs3	fibroblast growth factor receptor substrate 3	gene	MP:0030250	frontonasal prominence hypoplasia		IAGP		N	RGD:5509061	20180301	MGI			PMID:28483978
1321012	Mff	mitochondrial fission factor	gene	MP:0001657	abnormal induced morbidity/mortality		IAGP		N	RGD:5509061	20180524	MGI			PMID:28288978
1321012	Mff	mitochondrial fission factor	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20180524	MGI			PMID:28288978
1321012	Mff	mitochondrial fission factor	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20180524	MGI			PMID:28288978
1321012	Mff	mitochondrial fission factor	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20220428	MGI			PMID:33476744
1321012	Mff	mitochondrial fission factor	gene	MP:0014467	increased sperm mitochondrial size		IAGP		N	RGD:5509061	20240613	MGI			PMID:33476744
1321016	Ap4m1	adaptor-related protein complex AP-4, mu 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1321016	Ap4m1	adaptor-related protein complex AP-4, mu 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20201022	MGI			
1321016	Ap4m1	adaptor-related protein complex AP-4, mu 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321016	Ap4m1	adaptor-related protein complex AP-4, mu 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1321016	Ap4m1	adaptor-related protein complex AP-4, mu 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321016	Ap4m1	adaptor-related protein complex AP-4, mu 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1321016	Ap4m1	adaptor-related protein complex AP-4, mu 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1321016	Ap4m1	adaptor-related protein complex AP-4, mu 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1321020	Gabpb1	GA repeat binding protein, beta 1	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18426908
1321020	Gabpb1	GA repeat binding protein, beta 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18426908
1321022	Prkd3	protein kinase D3	gene	MP:0000130	abnormal trabecular bone morphology		IEA		N	RGD:5509061	20111116	MGI			
1321022	Prkd3	protein kinase D3	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20111116	MGI			
1321022	Prkd3	protein kinase D3	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20111116	MGI			
1321022	Prkd3	protein kinase D3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20161117	MGI			PMID:27670070
1321022	Prkd3	protein kinase D3	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20161117	MGI			PMID:27670070
1321022	Prkd3	protein kinase D3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1321022	Prkd3	protein kinase D3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321022	Prkd3	protein kinase D3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1321022	Prkd3	protein kinase D3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1321022	Prkd3	protein kinase D3	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20240523	MGI			
1321022	Prkd3	protein kinase D3	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20161117	MGI			PMID:27670070
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754854
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11778047
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417422
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11778047
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417422
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11778047
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417422
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754854
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754854
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754854
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11778047
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417422
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754854
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754854
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754854
1321025	Man2a2	mannosidase 2, alpha 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754854
1321027	Gp1ba	glycoprotein 1b, alpha polypeptide	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706630
1321027	Gp1ba	glycoprotein 1b, alpha polypeptide	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706630
1321027	Gp1ba	glycoprotein 1b, alpha polypeptide	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17382885
1321027	Gp1ba	glycoprotein 1b, alpha polypeptide	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706630
1321027	Gp1ba	glycoprotein 1b, alpha polypeptide	gene	MP:0030025	giant platelets		IAGP		N	RGD:5509061	20170803	MGI			PMID:10706630
1321028	Mettl2	methyltransferase 2, methylcytidine	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20170713	MGI			PMID:28655767
1321034	Ccl24	C-C motif chemokine ligand 24	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647285
1321034	Ccl24	C-C motif chemokine ligand 24	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16210640
1321034	Ccl24	C-C motif chemokine ligand 24	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16210640
1321034	Ccl24	C-C motif chemokine ligand 24	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
1321034	Ccl24	C-C motif chemokine ligand 24	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841312
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841312
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841312
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841312
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841312
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841312
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841312
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841312
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0009287	decreased abdominal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0031414	decreased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23173044
1321036	Cdkal1	CDK5 regulatory subunit associated protein 1-like 1	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23173044
1321039	Msgn1	mesogenin 1	gene	MP:0000138	absent vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0000151	absent ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0000962	disorganized dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0003401	enlarged tail bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0004197	abnormal fetal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0012182	abnormal presomitic mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0012184	absent paraxial mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0012277	increased tail bud apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321039	Msgn1	mesogenin 1	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124811
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20190509	MGI			PMID:24888588
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20190509	MGI			PMID:24888588
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0003134	increased late pro-B cell number		IAGP		N	RGD:5509061	20190509	MGI			PMID:24888588
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20240523	MGI			
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20190509	MGI			PMID:24888588
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20190509	MGI			PMID:24888588
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0009198	abnormal male genitalia morphology		IEA		N	RGD:5509061	20230720	MGI			
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20190509	MGI			PMID:24888588
1321042	Mzb1	marginal zone B and B1 cell-specific protein 1	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20190509	MGI			PMID:24888588
1321044	Ano4	anoctamin 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1321044	Ano4	anoctamin 4	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20250508	MGI			
1321044	Ano4	anoctamin 4	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1321048	Tbc1d5	TBC1 domain family, member 5	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20240523	MGI			
1321048	Tbc1d5	TBC1 domain family, member 5	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201022	MGI			
1321048	Tbc1d5	TBC1 domain family, member 5	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1321050	Col9a3	collagen, type IX, alpha 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20200514	MGI			
1321050	Col9a3	collagen, type IX, alpha 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20200514	MGI			
1321050	Col9a3	collagen, type IX, alpha 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1321050	Col9a3	collagen, type IX, alpha 3	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20220811	MGI			
1321050	Col9a3	collagen, type IX, alpha 3	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20200514	MGI			
1321050	Col9a3	collagen, type IX, alpha 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:11058094
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537701
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7310489
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7310489
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7310489
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20210729	MGI			PMID:32016796
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10193444
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10193444
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9434937
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:9434937
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11058094
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001386	abnormal maternal nurturing		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001389	abnormal eye movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:7310489
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777251
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20210729	MGI			PMID:32016796
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777251
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6279728
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002082	postnatal lethality		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10193444
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:7310489
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002095	abnormal skin pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10193444
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777251
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777251
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002620	abnormal monocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777251
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20210729	MGI			PMID:32016796
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0002938	white spotting		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0003173	decreased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0004165	abnormal lateral geniculate nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7310489
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0004267	abnormal optic tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3584547
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0004721	abnormal platelet dense granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10381507
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:115747
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10381507
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11058094
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005060	accumulation of giant lysosomes in kidney/renal tubule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10381507
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11058094
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12445206
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9434937
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:115747
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537701
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9434937
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:11058094
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777251
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0005636	abnormal mineral homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11058094
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0006103	abnormal midbrain roof plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3584547
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777251
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0008028	pregnancy-related premature death		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0008258	thin endometrium		IAGP		N	RGD:5509061	20210729	MGI			PMID:32016796
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009088	thin uterine horn		IAGP		N	RGD:5509061	20210729	MGI			PMID:32016796
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009089	short uterine horn		IAGP		N	RGD:5509061	20210729	MGI			PMID:32016796
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009379	abnormal foot pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9434937
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9434937
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9434937
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009557	decreased platelet ADP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009557	decreased platelet ADP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9434937
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0009618	increased brain zinc level		IAGP		N	RGD:5509061	20251204	MGI			PMID:15537701
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0010815	enlarged alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777251
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0010950	abnormal lung hysteresivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12777251
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0011088	neonatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0011277	decreased tail pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0011279	decreased ear pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0014780	increased kidney enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:115747
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:6696991
1321052	Ap3b1	adaptor-related protein complex 3, beta 1 subunit	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
1321055	E2f7	E2F transcription factor 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18194653
1321055	E2f7	E2F transcription factor 7	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18194653
1321055	E2f7	E2F transcription factor 7	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18194653
1321055	E2f7	E2F transcription factor 7	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18194653
1321055	E2f7	E2F transcription factor 7	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18194653
1321055	E2f7	E2F transcription factor 7	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18194653
1321055	E2f7	E2F transcription factor 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18194653
1321055	E2f7	E2F transcription factor 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0008402	increased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18194653
1321055	E2f7	E2F transcription factor 7	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0008959	abnormal spongiotrophoblast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0009658	increased placenta apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18194653
1321055	E2f7	E2F transcription factor 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516201
1321055	E2f7	E2F transcription factor 7	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:18194653
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470499
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0003929	decreased heart rate variability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0004156	abnormal QT variability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0006110	ventricular fibrillation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0006277	abnormal parasympathetic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15470499
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077327
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0031734	doublet premature ventricular contraction		IAGP		N	RGD:5509061	20260716	MGI			PMID:12077327
1321060	Nhlh1	nescient helix loop helix 1	gene	MP:0031735	triplet premature ventricular contraction		IAGP		N	RGD:5509061	20260716	MGI			PMID:12077327
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20210826	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210826	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210826	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20210826	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210826	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18511420
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0009456	impaired cued conditioning behavior		IEA		N	RGD:5509061	20201022	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1321063	G2e3	G2/M-phase specific E3 ubiquitin ligase	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18511420
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200618	MGI			PMID:30415212
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20171116	MGI			PMID:28495971
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20200618	MGI			PMID:30415212
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20200618	MGI			PMID:30415212
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20200618	MGI			PMID:30415212
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20200618	MGI			PMID:30415212
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20200618	MGI			PMID:30415212
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20200618	MGI			PMID:30415212
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009377	ectopic manchette		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20200618	MGI			PMID:30415212
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0011677	abnormal olfactory sensory neuron physiology		IAGP		N	RGD:5509061	20171116	MGI			PMID:28495971
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20200618	MGI			PMID:30415212
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0030591	absent sperm fibrous sheath		IAGP		N	RGD:5509061	20220224	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:29606301
1321066	Cfap69	cilia and flagella associated protein 69	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:30415212
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000040	decreased middle ear ossicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000158	absent sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000158	absent sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000450	absent snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000453	absent mouth		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17984226
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000919	cranioschisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15198977
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001062	absent oculomotor nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001072	abnormal vestibulocochlear nerve morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428831
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428831
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672719
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12438097
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672719
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672719
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003388	absent pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003395	abnormal subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003873	pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004339	absent clavicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004379	wide frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004383	absent interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004383	absent interparietal bone		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004417	decreased cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004419	absent parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004468	small zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004472	broad nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004473	absent nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004673	splayed ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967920
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005174	abnormal tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005261	aniridia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006130	pulmonary valve atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006211	small orbits		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0008510	absent retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0009379	abnormal foot pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0009844	abnormal neural crest cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0009893	cleft primary palate		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010043	abnormal frontonasal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010043	abnormal frontonasal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010224	abnormal heart ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010241	abnormal aortic arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010572	persistent right dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622765
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8622766
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672719
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:11744375
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0012535	abnormal optic fissure closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918694
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0012747	abnormal cardiac neural crest cell morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0013550	abnormal secondary palate morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0021211	unilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:25381013
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030191	narrow snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:15181535
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030200	abnormal nasal septum cartilage morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:14975718
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030334	absent sixth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030337	enlarged third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030340	absent fourth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030341	fourth pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030341	fourth pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20171116	MGI			PMID:19855134
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030531	abnormal facial skin morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030532	abnormal periorbital skin morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:14975722
1321068	Tfap2a	transcription factor AP-2, alpha	gene	MP:0030579	thoracoabdominoschisis		IAGP		N	RGD:5509061	20180607	MGI			PMID:8622766
1321070	Thap11	THAP domain containing 11	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20220721	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18585351
1321070	Thap11	THAP domain containing 11	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18585351
1321070	Thap11	THAP domain containing 11	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1321070	Thap11	THAP domain containing 11	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18585351
1321070	Thap11	THAP domain containing 11	gene	MP:0030930	decreased digit pigmentation		IAGP		N	RGD:5509061	20220721	MGI			PMID:35013307
1321072	Mettl25	methyltransferase like 25	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20220519	MGI			
1321072	Mettl25	methyltransferase like 25	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1321075	Pkd2l2	polycystic kidney disease 2-like 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1321075	Pkd2l2	polycystic kidney disease 2-like 2	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20220421	MGI			
1321075	Pkd2l2	polycystic kidney disease 2-like 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1321075	Pkd2l2	polycystic kidney disease 2-like 2	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1321075	Pkd2l2	polycystic kidney disease 2-like 2	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1321075	Pkd2l2	polycystic kidney disease 2-like 2	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
1321075	Pkd2l2	polycystic kidney disease 2-like 2	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1321075	Pkd2l2	polycystic kidney disease 2-like 2	gene	MP:0031391	increased locomotor activity		IEA		N	RGD:5509061	20220421	MGI			
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210128	MGI			
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321077	Mark4	MAP/microtubule affinity regulating kinase 4	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:22992738
1321079	Clk4	CDC like kinase 4	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321079	Clk4	CDC like kinase 4	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321079	Clk4	CDC like kinase 4	gene	MP:0004093	diffuse Z line		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321079	Clk4	CDC like kinase 4	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321079	Clk4	CDC like kinase 4	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321079	Clk4	CDC like kinase 4	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321079	Clk4	CDC like kinase 4	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321079	Clk4	CDC like kinase 4	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321079	Clk4	CDC like kinase 4	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321079	Clk4	CDC like kinase 4	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20220915	MGI			PMID:35907876
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923632
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:17981124
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17981124
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15020257
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20200618	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20170504	MGI			PMID:26389676
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20170504	MGI			PMID:26389676
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0002869	increased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17981124
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20170504	MGI			PMID:26389676
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20170504	MGI			PMID:26389676
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17981124
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0003858	enhanced coordination		IEA		N	RGD:5509061	20141003	MGI			
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17981124
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20170504	MGI			PMID:26389676
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008112	abnormal monocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923632
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17981124
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0009488	abnormal pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18219322
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923632
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17981124
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20160225	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0014117	increased pancreatic beta cell apoptosis		IAGP		N	RGD:5509061	20160324	MGI			PMID:26596471
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:17981124
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:20457756
1321081	Senp1	SUMO1/sentrin specific peptidase 1	gene	MP:0031059	increased circulating C-reactive protein level		IAGP		N	RGD:5509061	20200618	MGI			PMID:26596471
1321084	Nfx1	nuclear transcription factor, X-box binding 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1321084	Nfx1	nuclear transcription factor, X-box binding 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20250508	MGI			
1321084	Nfx1	nuclear transcription factor, X-box binding 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1321084	Nfx1	nuclear transcription factor, X-box binding 1	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1321084	Nfx1	nuclear transcription factor, X-box binding 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1321084	Nfx1	nuclear transcription factor, X-box binding 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1321084	Nfx1	nuclear transcription factor, X-box binding 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1321087	Mccc2	methylcrotonoyl-Coenzyme A carboxylase 2 (beta)	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1321087	Mccc2	methylcrotonoyl-Coenzyme A carboxylase 2 (beta)	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1321087	Mccc2	methylcrotonoyl-Coenzyme A carboxylase 2 (beta)	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1321087	Mccc2	methylcrotonoyl-Coenzyme A carboxylase 2 (beta)	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1321087	Mccc2	methylcrotonoyl-Coenzyme A carboxylase 2 (beta)	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20221215	MGI			
1321087	Mccc2	methylcrotonoyl-Coenzyme A carboxylase 2 (beta)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321090	C2cd2l	C2 calcium-dependent domain containing 2-like	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1321090	C2cd2l	C2 calcium-dependent domain containing 2-like	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1321090	C2cd2l	C2 calcium-dependent domain containing 2-like	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20231207	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0000452	abnormal mouth morphology		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1321092	Ehf	ets homologous factor	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0001340	abnormal eyelid morphology		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20231207	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20231207	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1321092	Ehf	ets homologous factor	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1321092	Ehf	ets homologous factor	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20250508	MGI			
1321092	Ehf	ets homologous factor	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1321092	Ehf	ets homologous factor	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1321098	Adgrf1	adhesion G protein-coupled receptor F1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20240523	MGI			
1321098	Adgrf1	adhesion G protein-coupled receptor F1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20240523	MGI			
1321098	Adgrf1	adhesion G protein-coupled receptor F1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1321098	Adgrf1	adhesion G protein-coupled receptor F1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1321098	Adgrf1	adhesion G protein-coupled receptor F1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1321098	Adgrf1	adhesion G protein-coupled receptor F1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20231207	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20181227	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1321101	Zbtb43	zinc finger and BTB domain containing 43	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1321103	Pcdhb13	protocadherin beta 13	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210128	MGI			
1321103	Pcdhb13	protocadherin beta 13	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321103	Pcdhb13	protocadherin beta 13	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1321103	Pcdhb13	protocadherin beta 13	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1321103	Pcdhb13	protocadherin beta 13	gene	MP:0002607	decreased basophil cell number		IEA		N	RGD:5509061	20221215	MGI			
1321103	Pcdhb13	protocadherin beta 13	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321103	Pcdhb13	protocadherin beta 13	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210128	MGI			
1321105	Psd4	pleckstrin and Sec7 domain containing 4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20250508	MGI			
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20250508	MGI			
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0004167	abnormal cingulate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0010009	abnormal piriform cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20160623	MGI			PMID:27038906
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0014814	increased brain glucose metabolism		IAGP		N	RGD:5509061	20251204	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0014956	decreased mitochondria enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22914734
1321107	Cox10	heme A:farnesyltransferase cytochrome c oxidase assembly factor 10	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:27038906
1321109	Snx2	sorting nexin 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1321109	Snx2	sorting nexin 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1321109	Snx2	sorting nexin 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1321109	Snx2	sorting nexin 2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1321109	Snx2	sorting nexin 2	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1321109	Snx2	sorting nexin 2	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1321109	Snx2	sorting nexin 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1321109	Snx2	sorting nexin 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388759
1321109	Snx2	sorting nexin 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1321109	Snx2	sorting nexin 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1321109	Snx2	sorting nexin 2	gene	MP:0020515	abnormal visceral yolk sac endoderm morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:12388759
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20190502	MGI			
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20161201	MGI			
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20161201	MGI			
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20211021	MGI			
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20211021	MGI			
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321110	Bicdl1	BICD family like cargo adaptor 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347093
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210520	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220519	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20210520	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210520	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347093
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210520	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0003948	abnormal gas homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0009130	increased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19066220
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347093
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371609
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928865
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347093
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0031204	hindlimb paresis		IAGP		N	RGD:5509061	20210218	MGI			PMID:24191050
1321112	Ncor2	nuclear receptor co-repressor 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:20371609
1321114	Perp	PERP, TP53 apoptosis effector	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614825
1321114	Perp	PERP, TP53 apoptosis effector	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614825
1321114	Perp	PERP, TP53 apoptosis effector	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975948
1321114	Perp	PERP, TP53 apoptosis effector	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614825
1321114	Perp	PERP, TP53 apoptosis effector	gene	MP:0009581	decreased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975948
1321114	Perp	PERP, TP53 apoptosis effector	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975948
1321114	Perp	PERP, TP53 apoptosis effector	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:20975948
1321114	Perp	PERP, TP53 apoptosis effector	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614825
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0003344	mammary gland hypoplasia		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160811	MGI			
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20170706	MGI			PMID:28162974
1321118	Ube2o	ubiquitin-conjugating enzyme E2O	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:28162974
1321120	Hoxb1	homeobox B1	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1321120	Hoxb1	homeobox B1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15861402
1321120	Hoxb1	homeobox B1	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15198977
1321120	Hoxb1	homeobox B1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0000843	absent facial nuclei		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0000843	absent facial nuclei		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1321120	Hoxb1	homeobox B1	gene	MP:0000909	abnormal facial motor nucleus morphology		IEA		N	RGD:5509061	20141003	MGI			
1321120	Hoxb1	homeobox B1	gene	MP:0000910	small facial motor nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0000910	small facial motor nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15198977
1321120	Hoxb1	homeobox B1	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14960494
1321120	Hoxb1	homeobox B1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15198977
1321120	Hoxb1	homeobox B1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967950
1321120	Hoxb1	homeobox B1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0001490	abnormal vibrissae reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15198977
1321120	Hoxb1	homeobox B1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15198977
1321120	Hoxb1	homeobox B1	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0001993	abnormal blinking		IAGP		N	RGD:5509061	20141003	MGI			PMID:15198977
1321120	Hoxb1	homeobox B1	gene	MP:0001993	abnormal blinking		IAGP		N	RGD:5509061	20171005	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12815623
1321120	Hoxb1	homeobox B1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15198977
1321120	Hoxb1	homeobox B1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532923
1321120	Hoxb1	homeobox B1	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15861402
1321120	Hoxb1	homeobox B1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0004235	abnormal masseter muscle morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0004239	abnormal temporalis muscle morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1321120	Hoxb1	homeobox B1	gene	MP:0004561	absent facial nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1321120	Hoxb1	homeobox B1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1321120	Hoxb1	homeobox B1	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0006334	abnormal susceptibility to hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1321120	Hoxb1	homeobox B1	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0008372	small malleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155191
1321120	Hoxb1	homeobox B1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967950
1321120	Hoxb1	homeobox B1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967950
1321120	Hoxb1	homeobox B1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1321120	Hoxb1	homeobox B1	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0012490	abnormal cochlear VIII nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408898
1321120	Hoxb1	homeobox B1	gene	MP:0012524	abnormal lower lip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0012746	abnormal neural crest cell delamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11532923
1321120	Hoxb1	homeobox B1	gene	MP:0012796	abnormal rhombomere 4 morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967950
1321120	Hoxb1	homeobox B1	gene	MP:0012799	absent rhombomere 4		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0012803	absent rhombomere 5		IAGP		N	RGD:5509061	20141003	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0013224	absent second pharyngeal pouch		IAGP		N	RGD:5509061	20150101	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0013225	abnormal third pharyngeal pouch morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0014747	abnormal motor neuron axon guidance		IAGP		N	RGD:5509061	20250904	MGI			PMID:8967950
1321120	Hoxb1	homeobox B1	gene	MP:0030040	absent facial muscle		IAGP		N	RGD:5509061	20170921	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0030040	absent facial muscle		IAGP		N	RGD:5509061	20170921	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0030067	narrow face		IAGP		N	RGD:5509061	20170921	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0030106	small incus		IAGP		N	RGD:5509061	20171005	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0030141	facial paralysis		IAGP		N	RGD:5509061	20171005	MGI			PMID:16890163
1321120	Hoxb1	homeobox B1	gene	MP:0030141	facial paralysis		IAGP		N	RGD:5509061	20171005	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0030142	facial muscle degeneration		IAGP		N	RGD:5509061	20171005	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0030146	abnormal digastric posterior belly morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0030146	abnormal digastric posterior belly morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0030149	abnormal stylohyoid muscle morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0030151	abnormal buccinator muscle morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0030152	abnormal depressor anguli oris muscle morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0030174	absent orbicularis oculi muscle		IAGP		N	RGD:5509061	20171005	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0030177	absent levator labii superioris muscle		IAGP		N	RGD:5509061	20171005	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0030184	abnormal zygomaticus muscle morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:8898234
1321120	Hoxb1	homeobox B1	gene	MP:0030207	absent zygomaticus muscle		IAGP		N	RGD:5509061	20171019	MGI			PMID:10529420
1321120	Hoxb1	homeobox B1	gene	MP:0030430	absent levator nasolabialis muscle		IAGP		N	RGD:5509061	20171214	MGI			PMID:8898234
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805292
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805292
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810604
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810604
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810604
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554819
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805292
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805292
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11805292
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810604
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810604
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0030934	decreased primordial germ cell proliferation		IAGP		N	RGD:5509061	20190411	MGI			PMID:12810604
1321122	Pin1	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:11805292
1321124	Plekhg1	pleckstrin homology and RhoGEF domain containing G1	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268034
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15299027
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15299027
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15299027
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15299027
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15299027
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268034
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0003085	abnormal egg cylinder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268034
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15299027
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268034
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268034
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18268034
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0010039	abnormal trophoblast giant cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15299027
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15299027
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15299027
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0013589	thymus medulla hypoplasia		IAGP		N	RGD:5509061	20150319	MGI			PMID:18268034
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:20802511
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220210	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220303	MGI			PMID:31373619
1321126	Cops5	COP9 signalosome subunit 5	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:31373619
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11839819
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20151203	MGI			PMID:20376065
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0002748	abnormal pulmonary valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20151203	MGI			PMID:19273593
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:19409519
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:19409519
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:19409519
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20151203	MGI			PMID:19273593
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0010618	enlarged mitral valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0010620	thick mitral valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0010620	thick mitral valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0010629	thick tricuspid valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0010629	thick tricuspid valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:14993236
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20151203	MGI			PMID:19409519
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20151203	MGI			PMID:19409519
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0012193	increased keratinocyte migration		IAGP		N	RGD:5509061	20151203	MGI			PMID:20376065
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0031558	tricuspid valve hyperplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0031581	semilunar valve hyperplasia		IAGP		N	RGD:5509061	20240125	MGI			PMID:15936750
1321128	Adam9	ADAM metallopeptidase domain 9	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:19409519
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20220217	MGI			PMID:34339838
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20220217	MGI			PMID:34339838
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20220217	MGI			PMID:34339838
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20220217	MGI			PMID:34339838
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0010580	decreased heart left ventricle size		IAGP		N	RGD:5509061	20220217	MGI			PMID:34339838
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20220217	MGI			PMID:34339838
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20220217	MGI			PMID:34339838
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20220217	MGI			PMID:34339838
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20220217	MGI			PMID:34339838
1321131	Fam120b	family with sequence similarity 120, member B	gene	MP:0031609	increased fetal cardiomyocyte size		IAGP		N	RGD:5509061	20240321	MGI			PMID:34339838
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738763
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20201022	MGI			
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738763
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738763
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738763
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738763
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14738763
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1321133	Ubash3a	ubiquitin associated and SH3 domain containing, A	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1321135	Mtmr4	myotubularin related protein 4	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20160804	MGI			
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:18729827
1321138	Ptcd2	pentatricopeptide repeat domain 2	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:18729827
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20250626	MGI			PMID:37968726
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250612	MGI			PMID:23096007
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:30478397
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20210819	MGI			PMID:30478397
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0004019	abnormal vitamin homeostasis		IAGP		N	RGD:5509061	20250612	MGI			PMID:23096007
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20250612	MGI			PMID:23096007
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:30478397
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:37968726
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20210819	MGI			PMID:30478397
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:23096007
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20250612	MGI			PMID:23096007
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20250612	MGI			PMID:23096007
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20210819	MGI			PMID:30478397
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20250612	MGI			PMID:23096007
1321140	Qprt	quinolinate phosphoribosyltransferase	gene	MP:0012462	decreased brain internal capsule size		IAGP		N	RGD:5509061	20250626	MGI			PMID:37968726
1321141	Kif7	kinesin family member 7	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592253
1321141	Kif7	kinesin family member 7	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592253
1321141	Kif7	kinesin family member 7	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1321141	Kif7	kinesin family member 7	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1321141	Kif7	kinesin family member 7	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592253
1321141	Kif7	kinesin family member 7	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321141	Kif7	kinesin family member 7	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592253
1321141	Kif7	kinesin family member 7	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592253
1321141	Kif7	kinesin family member 7	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1321141	Kif7	kinesin family member 7	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321141	Kif7	kinesin family member 7	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321141	Kif7	kinesin family member 7	gene	MP:0003936	abnormal reproductive system development		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0004157	interrupted aortic arch		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0004949	absent neuronal precursor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0005170	cleft upper lip		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1321141	Kif7	kinesin family member 7	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321141	Kif7	kinesin family member 7	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592253
1321141	Kif7	kinesin family member 7	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321141	Kif7	kinesin family member 7	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592253
1321141	Kif7	kinesin family member 7	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1321141	Kif7	kinesin family member 7	gene	MP:0009744	postaxial polydactyly		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321141	Kif7	kinesin family member 7	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0010460	pulmonary artery hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0010975	abnormal lung lobe morphology		IEA		N	RGD:5509061	20141003	MGI			
1321141	Kif7	kinesin family member 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549984
1321141	Kif7	kinesin family member 7	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1321141	Kif7	kinesin family member 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666503
1321141	Kif7	kinesin family member 7	gene	MP:0012059	thick diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321141	Kif7	kinesin family member 7	gene	MP:0012060	diaphragm muscle hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321141	Kif7	kinesin family member 7	gene	MP:0012061	abnormal diaphragm central tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321141	Kif7	kinesin family member 7	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650387
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20191128	MGI			
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191128	MGI			
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20240523	MGI			
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20240523	MGI			
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011249	abdominal situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20221215	MGI			
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0011649	immotile respiratory cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23525783
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0012277	increased tail bud apoptosis		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0013197	decreased embryonic cilium number		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20191128	MGI			PMID:31107948
1321143	Dnaaf2	dynein, axonemal assembly factor 2	gene	MP:0030963	abnormal brain ependyma motile cilium location or orientation		IAGP		N	RGD:5509061	20190725	MGI			PMID:23525783
1321147	Farsa	phenylalanyl-tRNA synthetase, alpha subunit	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
1321147	Farsa	phenylalanyl-tRNA synthetase, alpha subunit	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1321147	Farsa	phenylalanyl-tRNA synthetase, alpha subunit	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1321147	Farsa	phenylalanyl-tRNA synthetase, alpha subunit	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20150108	MGI			
1321147	Farsa	phenylalanyl-tRNA synthetase, alpha subunit	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1321147	Farsa	phenylalanyl-tRNA synthetase, alpha subunit	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20150430	MGI			
1321147	Farsa	phenylalanyl-tRNA synthetase, alpha subunit	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20150108	MGI			
1321147	Farsa	phenylalanyl-tRNA synthetase, alpha subunit	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1321147	Farsa	phenylalanyl-tRNA synthetase, alpha subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321148	Prox2	prospero homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470382
1321148	Prox2	prospero homeobox 2	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20190502	MGI			
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0010493	abnormal atrium myocardium morphology		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321150	Pabir1	PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1	gene	MP:0012501	abnormal pericardial cavity morphology		IAGP		N	RGD:5509061	20240905	MGI			PMID:36715298
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321152	Kbtbd2	kelch repeat and BTB (POZ) domain containing 2	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20161124	MGI			PMID:27708159
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20181227	MGI			
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20210805	MGI			PMID:34026442
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0012768	decreased KLRG1-positive NK cell number		IEA		N	RGD:5509061	20201022	MGI			
1321154	Cnot4	CCR4-NOT transcription complex, subunit 4	gene	MP:0013406	abnormal epidermal immune compartment		IEA		N	RGD:5509061	20201231	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20260402	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20260402	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20181227	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20260402	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20260402	MGI			
1321158	Me2	malic enzyme 2, NAD(+)-dependent, mitochondrial	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20260402	MGI			
1321160	Slc39a5	solute carrier family 39 (metal ion transporter), member 5	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20220519	MGI			
1321160	Slc39a5	solute carrier family 39 (metal ion transporter), member 5	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1321160	Slc39a5	solute carrier family 39 (metal ion transporter), member 5	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24303081
1321160	Slc39a5	solute carrier family 39 (metal ion transporter), member 5	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1321160	Slc39a5	solute carrier family 39 (metal ion transporter), member 5	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24303081
1321160	Slc39a5	solute carrier family 39 (metal ion transporter), member 5	gene	MP:0009150	pancreatic acinar cell atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24303081
1321160	Slc39a5	solute carrier family 39 (metal ion transporter), member 5	gene	MP:0009615	abnormal zinc homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24303081
1321160	Slc39a5	solute carrier family 39 (metal ion transporter), member 5	gene	MP:0011924	abnormal liver zinc level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24303081
1321161	Frmd8	FERM domain containing 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20181108	MGI			PMID:29897336
1321161	Frmd8	FERM domain containing 8	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20231130	MGI			PMID:37527040
1321161	Frmd8	FERM domain containing 8	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20231130	MGI			PMID:37527040
1321161	Frmd8	FERM domain containing 8	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20231130	MGI			PMID:37527040
1321161	Frmd8	FERM domain containing 8	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20231130	MGI			PMID:37527040
1321161	Frmd8	FERM domain containing 8	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20231130	MGI			PMID:37527040
1321161	Frmd8	FERM domain containing 8	gene	MP:0013955	increased colon length		IAGP		N	RGD:5509061	20231130	MGI			PMID:37527040
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321162	Zswim7	zinc finger SWIM-type containing 7	gene	MP:0013507	increased ovary apoptosis		IAGP		N	RGD:5509061	20190502	MGI			PMID:30305635
1321164	Chchd3	coiled-coil-helix-coiled-coil-helix domain containing 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1321164	Chchd3	coiled-coil-helix-coiled-coil-helix domain containing 3	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20260402	MGI			
1321164	Chchd3	coiled-coil-helix-coiled-coil-helix domain containing 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1321164	Chchd3	coiled-coil-helix-coiled-coil-helix domain containing 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1321164	Chchd3	coiled-coil-helix-coiled-coil-helix domain containing 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1321164	Chchd3	coiled-coil-helix-coiled-coil-helix domain containing 3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1321164	Chchd3	coiled-coil-helix-coiled-coil-helix domain containing 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210826	MGI			
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240801	MGI			PMID:38597936
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20240801	MGI			PMID:38597936
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20210826	MGI			
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0005102	abnormal iris pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38597936
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38597936
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20240801	MGI			PMID:38597936
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0009235	small sperm head		IAGP		N	RGD:5509061	20240801	MGI			PMID:38597936
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210826	MGI			
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20240801	MGI			PMID:38597936
1321165	Ccdc28a	coiled-coil domain containing 28A	gene	MP:0030980	abnormal acroplaxome morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38597936
1321167	Stab1	stabilin 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0011009	increased circulating glutamate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321167	Stab1	stabilin 1	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21293057
1321169	Pcdhb22	protocadherin beta 22	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1321169	Pcdhb22	protocadherin beta 22	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1321169	Pcdhb22	protocadherin beta 22	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:7203014
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7203014
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7089489
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7203014
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12445206
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0008731	abnormal hair shaft melanin granule morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:7203014
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0009779	enhanced behavioral response to anesthetic		IAGP		N	RGD:5509061	20141003	MGI			PMID:2513223
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7089489
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0011277	decreased tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7203014
1321174	Bloc1s3	biogenesis of lysosomal organelles complex-1, subunit 3	gene	MP:0011279	decreased ear pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7203014
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0000929	open neural tube		IEA		N	RGD:5509061	20111116	MGI			
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20160324	MGI			PMID:26474913
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160324	MGI			PMID:26474913
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20160324	MGI			PMID:26474913
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20160324	MGI			PMID:26474913
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20160324	MGI			PMID:26474913
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0003400	kinked neural tube		IEA		N	RGD:5509061	20111116	MGI			
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0003794	delayed somite formation		IEA		N	RGD:5509061	20111116	MGI			
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0003885	abnormal rostral-caudal body axis extension		IEA		N	RGD:5509061	20111116	MGI			
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0009455	enhanced cued conditioning behavior		IAGP		N	RGD:5509061	20160324	MGI			PMID:26474913
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0009768	impaired somite development		IEA		N	RGD:5509061	20111116	MGI			
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160324	MGI			PMID:26474913
1321176	Cyfip1	cytoplasmic FMR1 interacting protein 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1321178	Itga3	integrin alpha 3	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1321178	Itga3	integrin alpha 3	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20241121	MGI			
1321178	Itga3	integrin alpha 3	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19104148
1321178	Itga3	integrin alpha 3	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1321178	Itga3	integrin alpha 3	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1321178	Itga3	integrin alpha 3	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904471
1321178	Itga3	integrin alpha 3	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904471
1321178	Itga3	integrin alpha 3	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17848500
1321178	Itga3	integrin alpha 3	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1321178	Itga3	integrin alpha 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19104148
1321178	Itga3	integrin alpha 3	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1321178	Itga3	integrin alpha 3	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792458
1321178	Itga3	integrin alpha 3	gene	MP:0003591	urethra atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0003826	abnormal Mullerian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0003827	abnormal Wolffian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241121	MGI			
1321178	Itga3	integrin alpha 3	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0004202	pulmonary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19104148
1321178	Itga3	integrin alpha 3	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20241121	MGI			
1321178	Itga3	integrin alpha 3	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792458
1321178	Itga3	integrin alpha 3	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0004757	abnormal distal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118220
1321178	Itga3	integrin alpha 3	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19104148
1321178	Itga3	integrin alpha 3	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0008138	absent podocyte foot process		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0008509	disorganized retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0009252	absent urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0009569	abnormal left lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0009570	abnormal right lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792458
1321178	Itga3	integrin alpha 3	gene	MP:0010116	abnormal primitive urogenital sinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19104148
1321178	Itga3	integrin alpha 3	gene	MP:0010896	decreased lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19104148
1321178	Itga3	integrin alpha 3	gene	MP:0010897	abnormal bronchiole epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0011011	impaired lung lobe morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0011032	impaired branching involved in terminal bronchiole morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433923
1321178	Itga3	integrin alpha 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1321178	Itga3	integrin alpha 3	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0011359	decreased glomerular capillary number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015618
1321178	Itga3	integrin alpha 3	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0011846	decreased kidney collecting duct number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951069
1321178	Itga3	integrin alpha 3	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:17848500
1321178	Itga3	integrin alpha 3	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:10433923
1321182	Ccl19	C-C motif chemokine ligand 19	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893676
1321182	Ccl19	C-C motif chemokine ligand 19	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893676
1321186	Psca	prostate stem cell antigen	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20170105	MGI			
1321186	Psca	prostate stem cell antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18044730
1321186	Psca	prostate stem cell antigen	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18044730
1321186	Psca	prostate stem cell antigen	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18044730
1321186	Psca	prostate stem cell antigen	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18044730
1321186	Psca	prostate stem cell antigen	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1321191	Shprh	SNF2 histone linker PHD RING helicase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20181227	MGI			
1321191	Shprh	SNF2 histone linker PHD RING helicase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1321191	Shprh	SNF2 histone linker PHD RING helicase	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1321193	Dclre1b	DNA cross-link repair 1B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20551906
1321193	Dclre1b	DNA cross-link repair 1B	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20551906
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20260402	MGI			
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:24124512
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20150305	MGI			PMID:21337463
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20150305	MGI			PMID:21337463
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:24124512
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:21337463
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0011187	abnormal parietal endoderm morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:21337463
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:24124512
1321195	Mesd	mesoderm development LRP chaperone	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20150305	MGI			PMID:21337463
1321197	Dhx38	DEAH-box helicase 38	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1321197	Dhx38	DEAH-box helicase 38	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1321197	Dhx38	DEAH-box helicase 38	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1321197	Dhx38	DEAH-box helicase 38	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1321197	Dhx38	DEAH-box helicase 38	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321197	Dhx38	DEAH-box helicase 38	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1321201	Tango2	transport and golgi organization 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1321201	Tango2	transport and golgi organization 2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1321202	Oas1c	2'-5' oligoadenylate synthetase 1C	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20221215	MGI			
1321202	Oas1c	2'-5' oligoadenylate synthetase 1C	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20221215	MGI			
1321202	Oas1c	2'-5' oligoadenylate synthetase 1C	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20221215	MGI			
1321202	Oas1c	2'-5' oligoadenylate synthetase 1C	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20221215	MGI			
1321202	Oas1c	2'-5' oligoadenylate synthetase 1C	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20221215	MGI			
1321202	Oas1c	2'-5' oligoadenylate synthetase 1C	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20221215	MGI			
1321202	Oas1c	2'-5' oligoadenylate synthetase 1C	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20221215	MGI			
1321202	Oas1c	2'-5' oligoadenylate synthetase 1C	gene	MP:0010574	dilated aorta		IEA		N	RGD:5509061	20250508	MGI			
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585967
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000080	abnormal exoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585967
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537796
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000151	absent ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585967
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20160616	MGI			PMID:26952979
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22190642
1321204	Cdx1	caudal type homeobox 1	gene	MP:0000963	fused dorsal root ganglion		IAGP		N	RGD:5509061	20160616	MGI			PMID:26952979
1321204	Cdx1	caudal type homeobox 1	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:26952979
1321204	Cdx1	caudal type homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19328777
1321204	Cdx1	caudal type homeobox 1	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20160616	MGI			PMID:26952979
1321204	Cdx1	caudal type homeobox 1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585967
1321204	Cdx1	caudal type homeobox 1	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004229	abnormal embryonic erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18511567
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537796
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537796
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537796
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1321204	Cdx1	caudal type homeobox 1	gene	MP:0004658	abnormal ventral tubercle of atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537796
1321204	Cdx1	caudal type homeobox 1	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585967
1321204	Cdx1	caudal type homeobox 1	gene	MP:0009784	abnormal melanoblast migration		IAGP		N	RGD:5509061	20160616	MGI			PMID:26952979
1321204	Cdx1	caudal type homeobox 1	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660544
1321204	Cdx1	caudal type homeobox 1	gene	MP:0030282	broad supraoccipital bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:7585967
1321205	Efcab14	EF-hand calcium binding domain 14	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20211021	MGI			
1321205	Efcab14	EF-hand calcium binding domain 14	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1321205	Efcab14	EF-hand calcium binding domain 14	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1321205	Efcab14	EF-hand calcium binding domain 14	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1321205	Efcab14	EF-hand calcium binding domain 14	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1321205	Efcab14	EF-hand calcium binding domain 14	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0000597	delayed hepatic development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21954064
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417726
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417726
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417726
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21954064
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21954064
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21954064
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21954064
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20230615	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0014010	abnormal peroxisome morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0014010	abnormal peroxisome morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:12417726
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0020847	abnormal peroxisome physiology		IAGP		N	RGD:5509061	20230615	MGI			PMID:12024045
1321209	Pex11b	peroxisomal biogenesis factor 11 beta	gene	MP:0020847	abnormal peroxisome physiology		IAGP		N	RGD:5509061	20230615	MGI			PMID:12417726
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160421	MGI			
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542455
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20240229	MGI			PMID:30718289
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542455
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20240229	MGI			PMID:30718289
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:30718289
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0010802	abnormal intestinal enteroendocrine cell morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20240229	MGI			PMID:30718289
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20240229	MGI			PMID:30718289
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542455
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240229	MGI			PMID:30718289
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240229	MGI			PMID:30718289
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0011525	abnormal placenta intervillous maternal lacunae morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:30718289
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0013485	increased Paneth cell number		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:22542455
1321211	Usp22	ubiquitin specific peptidase 22	gene	MP:0013794	abnormal intestinal villus goblet cell morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:26431380
1321215	Tnpo2	transportin 2 (importin 3, karyopherin beta 2b)	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1321215	Tnpo2	transportin 2 (importin 3, karyopherin beta 2b)	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20250508	MGI			
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0003326	liver failure		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20191205	MGI			PMID:25453901
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1321218	Uri1	URI1, prefoldin-like chaperone	gene	MP:0014782	increased liver enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:25453901
1321220	Ldb1	LIM domain binding 1	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390196
1321220	Ldb1	LIM domain binding 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15857913
1321220	Ldb1	LIM domain binding 1	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664423
1321220	Ldb1	LIM domain binding 1	gene	MP:0000853	absent cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664423
1321220	Ldb1	LIM domain binding 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664423
1321220	Ldb1	LIM domain binding 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23390196
1321220	Ldb1	LIM domain binding 1	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15857913
1321220	Ldb1	LIM domain binding 1	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15857913
1321220	Ldb1	LIM domain binding 1	gene	MP:0004713	split notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0008391	abnormal primordial germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0011363	renal glomerulus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0011455	absent glomerular endothelium fenestra		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0011483	renal glomerular synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1321220	Ldb1	LIM domain binding 1	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0012156	rostral-caudal axis duplication		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0012181	increased somite number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0012792	abnormal rhombomere 3 morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0012800	abnormal rhombomere 5 morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490556
1321220	Ldb1	LIM domain binding 1	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0030536	abnormal diastema morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1321220	Ldb1	LIM domain binding 1	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:23390196
1321221	Kif18b	kinesin family member 18B	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1321221	Kif18b	kinesin family member 18B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0000135	decreased compact bone thickness		IEA		N	RGD:5509061	20150917	MGI			
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20150917	MGI			
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0005451	abnormal body composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321223	Samd4	sterile alpha motif domain containing 4	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24799716
1321230	Sel1l3	sel-1 suppressor of lin-12-like 3 (C. elegans)	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1321230	Sel1l3	sel-1 suppressor of lin-12-like 3 (C. elegans)	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1321230	Sel1l3	sel-1 suppressor of lin-12-like 3 (C. elegans)	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1321232	Snx18	sorting nexin 18	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1321232	Snx18	sorting nexin 18	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16700072
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17133501
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16700072
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17133501
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1321236	Sfrp5	secreted frizzled-related sequence protein 5	gene	MP:0030324	abnormal anterior head development		IAGP		N	RGD:5509061	20180118	MGI			PMID:17133501
1321238	Tlk1	tousled-like kinase 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1321238	Tlk1	tousled-like kinase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1321238	Tlk1	tousled-like kinase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1321238	Tlk1	tousled-like kinase 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1321238	Tlk1	tousled-like kinase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1321238	Tlk1	tousled-like kinase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1321238	Tlk1	tousled-like kinase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1321238	Tlk1	tousled-like kinase 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20230601	MGI			
1321238	Tlk1	tousled-like kinase 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1321238	Tlk1	tousled-like kinase 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1321238	Tlk1	tousled-like kinase 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1321240	Cfap161	cilia and flagella associated protein 161	gene	MP:0000452	abnormal mouth morphology		IEA		N	RGD:5509061	20230119	MGI			
1321240	Cfap161	cilia and flagella associated protein 161	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20230119	MGI			
1321240	Cfap161	cilia and flagella associated protein 161	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20230119	MGI			
1321240	Cfap161	cilia and flagella associated protein 161	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1321240	Cfap161	cilia and flagella associated protein 161	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1321240	Cfap161	cilia and flagella associated protein 161	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20211104	MGI			PMID:34172766
1321240	Cfap161	cilia and flagella associated protein 161	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20230119	MGI			
1321240	Cfap161	cilia and flagella associated protein 161	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230119	MGI			
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769894
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107644
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107644
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769894
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107644
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855450
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18558633
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107644
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855450
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855450
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107644
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855450
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18558633
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769894
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18558633
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18558633
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:18558633
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18558633
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18558633
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107644
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16321985
1321242	Als2	alsin Rho guanine nucleotide exchange factor	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107644
1321244	Tuft1	tuftelin 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160114	MGI			
1321244	Tuft1	tuftelin 1	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0001340	abnormal eyelid morphology		IEA		N	RGD:5509061	20160211	MGI			
1321244	Tuft1	tuftelin 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201022	MGI			
1321244	Tuft1	tuftelin 1	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20170105	MGI			
1321244	Tuft1	tuftelin 1	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1321244	Tuft1	tuftelin 1	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0004241	acantholysis		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20160211	MGI			
1321244	Tuft1	tuftelin 1	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0013027	wounding		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321244	Tuft1	tuftelin 1	gene	MP:0030578	decreased keratinocyte adhesion		IAGP		N	RGD:5509061	20231019	MGI			PMID:37716648
1321246	Fbxo9	F-box protein 9	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1321246	Fbxo9	F-box protein 9	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321246	Fbxo9	F-box protein 9	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321246	Fbxo9	F-box protein 9	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1321246	Fbxo9	F-box protein 9	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1321246	Fbxo9	F-box protein 9	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1321246	Fbxo9	F-box protein 9	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1321247	Tsr1	TSR1 20S rRNA accumulation	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11595941
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11595941
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11595941
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11595941
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227845
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25675513
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20191226	MGI			PMID:11595941
1321253	Catsper1	cation channel, sperm associated 1	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:11595941
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0011200	abnormal extraembryonic coelom morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0011207	absent ectoplacental cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321255	Rangap1	RAN GTPase activating protein 1	gene	MP:0011208	small proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8314081
1321257	Arsa	arylsulfatase A	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10505624
1321257	Arsa	arylsulfatase A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10505624
1321257	Arsa	arylsulfatase A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430883
1321257	Arsa	arylsulfatase A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10505624
1321257	Arsa	arylsulfatase A	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430883
1321257	Arsa	arylsulfatase A	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430883
1321257	Arsa	arylsulfatase A	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430883
1321257	Arsa	arylsulfatase A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11430883
1321257	Arsa	arylsulfatase A	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9728336
1321257	Arsa	arylsulfatase A	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10505624
1321257	Arsa	arylsulfatase A	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0009853	decreased Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8962139
1321257	Arsa	arylsulfatase A	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321257	Arsa	arylsulfatase A	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20220203	MGI			PMID:21965315
1321259	Cd163	CD163 antigen	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20170525	MGI			PMID:26376364
1321259	Cd163	CD163 antigen	gene	MP:0002281	abnormal respiratory mucosa goblet cell morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26376364
1321259	Cd163	CD163 antigen	gene	MP:0003060	increased aerobic running capacity		IAGP		N	RGD:5509061	20170126	MGI			PMID:26242746
1321259	Cd163	CD163 antigen	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:26242746
1321259	Cd163	CD163 antigen	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20170126	MGI			PMID:26242746
1321259	Cd163	CD163 antigen	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20170126	MGI			PMID:26242746
1321259	Cd163	CD163 antigen	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20170126	MGI			PMID:26242746
1321259	Cd163	CD163 antigen	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20170126	MGI			PMID:26242746
1321259	Cd163	CD163 antigen	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20170126	MGI			PMID:26242746
1321259	Cd163	CD163 antigen	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:26242746
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20190502	MGI			
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321260	Pptc7	PTC7 protein phosphatase homolog	gene	MP:0020423	abnormal mitochondrial biogenesis		IAGP		N	RGD:5509061	20240620	MGI			PMID:31324765
1321261	Prr27	proline rich 27	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20201022	MGI			
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160421	MGI			
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0003405	abnormal platelet shape		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0003950	abnormal plasma membrane morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005635	decreased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974805
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0014060	abnormal platelet alpha-granule morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0014441	decreased response to leptin		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0020431	decreased platelet alpha-granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:26109204
1321267	Pik3c2a	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha	gene	MP:0031271	increased susceptibility to age-related hepatic steatosis		IAGP		N	RGD:5509061	20260730	MGI			PMID:27138914
1321271	Lgi2	leucine-rich repeat LGI family, member 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1321271	Lgi2	leucine-rich repeat LGI family, member 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1321271	Lgi2	leucine-rich repeat LGI family, member 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1321271	Lgi2	leucine-rich repeat LGI family, member 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1321271	Lgi2	leucine-rich repeat LGI family, member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1321273	Bend6	BEN domain containing 6	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20220811	MGI			
1321277	Cavin4	caveolae associated 4	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20150101	MGI			PMID:24567387
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0001202	skin photosensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0001202	skin photosensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0004147	increased porphyrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0005654	porphyria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0009545	abnormal dermis papillary layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0010163	hemolysis		IAGP		N	RGD:5509061	20201001	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0011414	erythruria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314073
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0012664	decreased circulating haptoglobin level		IAGP		N	RGD:5509061	20201001	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0014964	decreased circulating enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0014972	decreased spleen enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0015014	enhanced bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:16532394
1321279	Uros	uroporphyrinogen III synthase	gene	MP:0030058	erythrodontia		IAGP		N	RGD:5509061	20170921	MGI			PMID:16314073
1321282	Ankrd23	ankyrin repeat domain 23	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392382
1321282	Ankrd23	ankyrin repeat domain 23	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141225	MGI			PMID:24736439
1321282	Ankrd23	ankyrin repeat domain 23	gene	MP:0014920	increased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:17392382
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0004941	abnormal regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21130004
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0008573	increased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0008647	increased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0008769	abnormal plasmacytoid dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0009786	decreased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321285	Siglech	sialic acid binding Ig-like lectin H	gene	MP:0010220	decreased T-helper 17 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22177923
1321288	Hnrnpa2b1	heterogeneous nuclear ribonucleoprotein A2/B1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20201210	MGI			PMID:31320558
1321288	Hnrnpa2b1	heterogeneous nuclear ribonucleoprotein A2/B1	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20201210	MGI			PMID:31320558
1321288	Hnrnpa2b1	heterogeneous nuclear ribonucleoprotein A2/B1	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20201210	MGI			PMID:31320558
1321288	Hnrnpa2b1	heterogeneous nuclear ribonucleoprotein A2/B1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20201210	MGI			PMID:31320558
1321288	Hnrnpa2b1	heterogeneous nuclear ribonucleoprotein A2/B1	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20201210	MGI			PMID:31320558
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:31444330
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:31444330
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20191219	MGI			PMID:31444330
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20191219	MGI			PMID:31444330
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20191219	MGI			PMID:31444330
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20241121	MGI			
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20191219	MGI			PMID:31444330
1321294	Pkhd1l1	polycystic kidney and hepatic disease 1-like 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20191219	MGI			PMID:31444330
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149450
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149450
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23950734
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149450
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149450
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149450
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149450
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23950734
1321300	Topbp1	topoisomerase (DNA) II binding protein 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:21149450
1321304	Tti2	TELO2 interacting protein 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321304	Tti2	TELO2 interacting protein 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1321304	Tti2	TELO2 interacting protein 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1321304	Tti2	TELO2 interacting protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20240523	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210520	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20220811	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20210520	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230601	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20241121	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210520	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20220811	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151217	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0030081	small upper incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0030089	short lower incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0030090	short upper incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:26219237
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0030447	abnormal presphenoid synchondrosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:23026747
1321309	Evc2	EvC ciliary complex subunit 2	gene	MP:0030610	absent teeth		IEA		N	RGD:5509061	20210520	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20260402	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20250508	MGI			
1321310	Trmt2a	TRM2 tRNA methyltransferase 2A	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1321312	Nipsnap1	nipsnap homolog 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20141003	MGI			
1321312	Nipsnap1	nipsnap homolog 1	gene	MP:0003177	allodynia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22311985
1321312	Nipsnap1	nipsnap homolog 1	gene	MP:0003313	abnormal locomotor activation		IEA		N	RGD:5509061	20141003	MGI			
1321312	Nipsnap1	nipsnap homolog 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22311985
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169862
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0003578	absent ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0003582	abnormal ovary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11702780
1321315	Cpeb1	cytoplasmic polyadenylation element binding protein 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:11702780
1321318	Vstm4	V-set and transmembrane domain containing 4	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20240523	MGI			
1321318	Vstm4	V-set and transmembrane domain containing 4	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:31698979
1321318	Vstm4	V-set and transmembrane domain containing 4	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200402	MGI			PMID:31698979
1321318	Vstm4	V-set and transmembrane domain containing 4	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20200402	MGI			PMID:31698979
1321319	Zfp871	zinc finger protein 871	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1321319	Zfp871	zinc finger protein 871	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1321319	Zfp871	zinc finger protein 871	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1321319	Zfp871	zinc finger protein 871	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1321319	Zfp871	zinc finger protein 871	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321319	Zfp871	zinc finger protein 871	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230824	MGI			PMID:34257081
1321319	Zfp871	zinc finger protein 871	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1321325	5730455P16Rik	RIKEN cDNA 5730455P16 gene	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20241121	MGI			
1321325	5730455P16Rik	RIKEN cDNA 5730455P16 gene	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1321330	Rdm1	RAD52 motif 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1321330	Rdm1	RAD52 motif 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20141009	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20170105	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20141009	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000632	abnormal pineal gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000819	abnormal olfactory bulb morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321331	Setd5	SET domain containing 5	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321331	Setd5	SET domain containing 5	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170105	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20141009	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321331	Setd5	SET domain containing 5	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0002951	small thyroid gland		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0004032	abnormal interventricular groove morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0004201	fetal growth retardation		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20170105	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0004973	increased regulatory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321331	Setd5	SET domain containing 5	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0005358	abnormal incisor morphology		IEA		N	RGD:5509061	20201231	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160114	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0006064	abnormal superior vena cava morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20170105	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0008922	abnormal cervical rib		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20170105	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0010200	enlarged lymphatic vessel		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0010403	atrial septal defect		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0010422	heart right ventricle hypoplasia		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0010433	double inlet heart left ventricle		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0010436	abnormal coronary sinus morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0010484	bicuspid aortic valve		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0010487	abnormal right subclavian artery morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0010572	persistent right dorsal aorta		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0010595	abnormal aortic valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1321331	Setd5	SET domain containing 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321331	Setd5	SET domain containing 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0013809	absent pectinate muscle		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013810	absent brachiocephalic trunk		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013812	enlarged orbital veins		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013813	dilated hepatic portal vein		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013814	abnormal hepatic portal vein connection		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013842	ductus venosus stenosis		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013864	enlarged paraumbilical vein		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013874	abnormal ductus venosus topology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013878	abnormal ductus venosus valve topology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013925	abnormal vascular plexus formation		IAGP		N	RGD:5509061	20190321	MGI			PMID:27864380
1321331	Setd5	SET domain containing 5	gene	MP:0013948	intraembryonal intestine elongation		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013977	symmetric azygos veins		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0014000	anastomosis between internal carotid artery and basilar artery		IEA		N	RGD:5509061	20170504	MGI			
1321331	Setd5	SET domain containing 5	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861467
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0001422	abnormal drinking behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0002983	increased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861467
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0002983	increased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861467
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861467
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006095	absent amacrine cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861467
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006096	absent retina bipolar cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006097	abnormal cerebellar lobule formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006098	absent cerebellar lobules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006105	small tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105417
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11032813
1321333	Neurod4	neurogenic differentiation 4	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:15105417
1321335	Dcstamp	dendrocyte expressed seven transmembrane protein	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061724
1321335	Dcstamp	dendrocyte expressed seven transmembrane protein	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061724
1321335	Dcstamp	dendrocyte expressed seven transmembrane protein	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061724
1321335	Dcstamp	dendrocyte expressed seven transmembrane protein	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061724
1321335	Dcstamp	dendrocyte expressed seven transmembrane protein	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061724
1321335	Dcstamp	dendrocyte expressed seven transmembrane protein	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061724
1321335	Dcstamp	dendrocyte expressed seven transmembrane protein	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16061724
1321337	Sema4g	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1321337	Sema4g	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1321337	Sema4g	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1321337	Sema4g	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G	gene	MP:0004041	increased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20161201	MGI			PMID:25892012
1321337	Sema4g	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20161201	MGI			PMID:25892012
1321337	Sema4g	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G	gene	MP:0009964	abnormal cerebellum lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1321337	Sema4g	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1321339	Ddx47	DEAD box helicase 47	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1321339	Ddx47	DEAD box helicase 47	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1321339	Ddx47	DEAD box helicase 47	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1321341	Rgs11	regulator of G-protein signaling 11	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22547806
1321341	Rgs11	regulator of G-protein signaling 11	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22371490
1321341	Rgs11	regulator of G-protein signaling 11	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19535587
1321341	Rgs11	regulator of G-protein signaling 11	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22371490
1321341	Rgs11	regulator of G-protein signaling 11	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22547806
1321341	Rgs11	regulator of G-protein signaling 11	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19535587
1321341	Rgs11	regulator of G-protein signaling 11	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22371490
1321341	Rgs11	regulator of G-protein signaling 11	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19535587
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004773
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004773
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0000505	decreased digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004773
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0000507	absent digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004773
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20241121	MGI			
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20200514	MGI			
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20201022	MGI			
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0004137	abnormal gastric surface mucous cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004773
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004773
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20150312	MGI			PMID:19004773
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004773
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321345	Slc26a9	solute carrier family 26, member 9	gene	MP:0013566	dilated gastric gland		IAGP		N	RGD:5509061	20150312	MGI			PMID:19004773
1321349	Endod1	endonuclease domain containing 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1321349	Endod1	endonuclease domain containing 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1321349	Endod1	endonuclease domain containing 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1321349	Endod1	endonuclease domain containing 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1321349	Endod1	endonuclease domain containing 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1321353	Gemin5	gem nuclear organelle associated protein 5	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20240523	MGI			
1321353	Gemin5	gem nuclear organelle associated protein 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321353	Gemin5	gem nuclear organelle associated protein 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1321355	Irf5	interferon regulatory factor 5	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20200402	MGI			
1321355	Irf5	interferon regulatory factor 5	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111215	MGI			
1321355	Irf5	interferon regulatory factor 5	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665823
1321355	Irf5	interferon regulatory factor 5	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665823
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665823
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665823
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665823
1321355	Irf5	interferon regulatory factor 5	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1321355	Irf5	interferon regulatory factor 5	gene	MP:0010836	decreased CD4-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1321355	Irf5	interferon regulatory factor 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0003402	decreased liver weight		IEA		N	RGD:5509061	20241121	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008077	abnormal CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195075
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20181227	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818394
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1321364	Tox	thymocyte selection-associated high mobility group box	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1321366	Zfp513	zinc finger protein 513	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1321366	Zfp513	zinc finger protein 513	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1321366	Zfp513	zinc finger protein 513	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1321366	Zfp513	zinc finger protein 513	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539150
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539150
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539150
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539150
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539150
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008175	absent follicular B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539150
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008523	absent lymph node germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539150
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0013247	placenta necrosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:9390694
1321368	Traf2	TNF receptor-associated factor 2	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:29539633
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150788
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466504
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20170706	MGI			PMID:25995473
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111215	MGI			
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:25995473
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9735355
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20170706	MGI			PMID:25995473
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0003151	absent tunnel of Corti		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150788
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0003152	abnormal pillar cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150788
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150788
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0003986	small cochlear ganglion		IAGP		N	RGD:5509061	20170706	MGI			PMID:25995473
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004298	vestibular ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004298	vestibular ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004298	vestibular ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004298	vestibular ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9735355
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004301	absent organ of Corti supporting cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004301	absent organ of Corti supporting cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004302	abnormal Deiters cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004306	small Rosenthal canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004308	abnormal basilar membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004312	absent pillar cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9735355
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004325	absent vestibular hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004328	decreased vestibular hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9735355
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004363	stria vascularis degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004397	absent cochlear inner hair cells		IAGP		N	RGD:5509061	20170706	MGI			PMID:25995473
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004403	absent cochlear outer hair cells		IAGP		N	RGD:5509061	20170706	MGI			PMID:25995473
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004405	absent cochlear hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004405	absent cochlear hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150788
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004405	absent cochlear hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004409	abnormal crista ampullaris neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004465	degeneration of organ of Corti supporting cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004518	absent vestibular hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004518	absent vestibular hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9735355
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004526	absent cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150788
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004526	absent cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004526	absent cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004526	absent cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9735355
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004530	absent outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004533	fused inner hair cell stereocilia		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004535	absent inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004535	absent inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004586	pillar cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004588	abnormal vestibular hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004588	abnormal vestibular hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9735355
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004589	abnormal cochlear hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004589	abnormal cochlear hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004590	absent Deiters cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12585968
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004597	increased susceptibility to noise-induced hearing loss		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20170706	MGI			PMID:25995473
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20170706	MGI			PMID:25995473
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004741	mixed hearing loss		IAGP		N	RGD:5509061	20170706	MGI			PMID:25995473
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100430
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0006276	abnormal autonomic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12466504
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20111116	MGI			
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0008105	increased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0008304	abnormal organ of Corti supporting cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10452377
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0010015	abnormal cuticular plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150788
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20171012	MGI			PMID:12466504
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254021
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256502
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20250724	MGI			PMID:32970669
1321372	Pou4f3	POU domain, class 4, transcription factor 3	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:32970669
1321374	Fbxw2	F-box and WD-40 domain protein 2	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321377	Rdh12	retinol dehydrogenase 12	gene	MP:0003011	delayed dark adaptation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17032653
1321377	Rdh12	retinol dehydrogenase 12	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17032653
1321377	Rdh12	retinol dehydrogenase 12	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17032653
1321377	Rdh12	retinol dehydrogenase 12	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17032653
1321377	Rdh12	retinol dehydrogenase 12	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130236
1321377	Rdh12	retinol dehydrogenase 12	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17032653
1321377	Rdh12	retinol dehydrogenase 12	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:17032653
1321394	Srf	serum response factor	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569937
1321394	Srf	serum response factor	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0000288	abnormal pericardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1321394	Srf	serum response factor	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1321394	Srf	serum response factor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1321394	Srf	serum response factor	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9799237
1321394	Srf	serum response factor	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9799237
1321394	Srf	serum response factor	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9799237
1321394	Srf	serum response factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9799237
1321394	Srf	serum response factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857797
1321394	Srf	serum response factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1321394	Srf	serum response factor	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0002976	vascular smooth muscle hypotrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569937
1321394	Srf	serum response factor	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9799237
1321394	Srf	serum response factor	gene	MP:0004032	abnormal interventricular groove morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1321394	Srf	serum response factor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1321394	Srf	serum response factor	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1321394	Srf	serum response factor	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0005314	absent thyroid gland		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1321394	Srf	serum response factor	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1321394	Srf	serum response factor	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1321394	Srf	serum response factor	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1321394	Srf	serum response factor	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591768
1321394	Srf	serum response factor	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1321394	Srf	serum response factor	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647354
1321394	Srf	serum response factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169892
1321394	Srf	serum response factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1321394	Srf	serum response factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15569937
1321394	Srf	serum response factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15929941
1321394	Srf	serum response factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9799237
1321394	Srf	serum response factor	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:16260633
1321394	Srf	serum response factor	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:16260633
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133398
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133398
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133398
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133398
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133398
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133398
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220519	MGI			
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133398
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23133398
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321396	Chtf18	CTF18, chromosome transmission fidelity factor 18	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:23133398
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210520	MGI			
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20210520	MGI			
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20210826	MGI			
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20210826	MGI			
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20210826	MGI			
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1321398	Togaram1	TOG array regulator of axonemal microtubules 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210520	MGI			
1321400	Hoga1	4-hydroxy-2-oxoglutarate aldolase 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20161117	MGI			PMID:26428388
1321400	Hoga1	4-hydroxy-2-oxoglutarate aldolase 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1321400	Hoga1	4-hydroxy-2-oxoglutarate aldolase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1321400	Hoga1	4-hydroxy-2-oxoglutarate aldolase 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1321400	Hoga1	4-hydroxy-2-oxoglutarate aldolase 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20161117	MGI			PMID:26428388
1321400	Hoga1	4-hydroxy-2-oxoglutarate aldolase 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20161117	MGI			PMID:26428388
1321400	Hoga1	4-hydroxy-2-oxoglutarate aldolase 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20240523	MGI			
1321405	Afg2a	AFG2 AAA ATPase homolog A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230720	MGI			
1321405	Afg2a	AFG2 AAA ATPase homolog A	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230720	MGI			
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20181115	MGI			PMID:24024552
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20520781
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275357
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220317	MGI			PMID:21208614
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275357
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275357
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275357
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220317	MGI			PMID:21208614
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220317	MGI			PMID:21208614
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275357
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:20520781
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0004382	abnormal hair follicle melanogenesis		IAGP		N	RGD:5509061	20181115	MGI			PMID:24024552
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0008732	reduced hair shaft melanin granule number		IAGP		N	RGD:5509061	20181115	MGI			PMID:24024552
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20520781
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:21208614
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:21208614
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0009233	enlarged sperm head		IAGP		N	RGD:5509061	20220317	MGI			PMID:21208614
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:21208614
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20520781
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321410	Hsp90b1	heat shock protein 90, beta (Grp94), member 1	gene	MP:0011198	absent proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634284
1321414	Slc46a2	solute carrier family 46, member 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684012
1321414	Slc46a2	solute carrier family 46, member 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684012
1321414	Slc46a2	solute carrier family 46, member 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684012
1321414	Slc46a2	solute carrier family 46, member 2	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684012
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000336	decreased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16640660
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884426
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9010048
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910194
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986312
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986312
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986312
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9010048
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9010048
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9010048
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002138	abnormal hepatobiliary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764671
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060023
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060023
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16640660
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0003254	bile duct inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16640660
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23023393
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620319
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060023
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16640660
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16640660
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008036	abnormal NK T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060023
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008217	abnormal B cell activation		IEA		N	RGD:5509061	20111116	MGI			
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699117
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764671
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060023
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008471	abnormal spleen primary B follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9010048
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0008904	abnormal mammary fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910194
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009297	decreased mammary fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910194
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764671
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009629	small brachial lymph nodes		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009632	small axillary lymph nodes		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009633	absent cervical lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11251123
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20170706	MGI			PMID:26116508
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0013741	absent thymus corticomedullary boundary		IAGP		N	RGD:5509061	20150430	MGI			PMID:10319865
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0013741	absent thymus corticomedullary boundary		IAGP		N	RGD:5509061	20150430	MGI			PMID:8299692
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0014130	thymus cyst		IAGP		N	RGD:5509061	20160324	MGI			PMID:17986312
1321417	Map3k14	mitogen-activated protein kinase kinase kinase 14	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:8299692
1321418	Syvn1	synovial apoptosis inhibitor 1, synoviolin	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975321
1321418	Syvn1	synovial apoptosis inhibitor 1, synoviolin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:24636985
1321418	Syvn1	synovial apoptosis inhibitor 1, synoviolin	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975321
1321418	Syvn1	synovial apoptosis inhibitor 1, synoviolin	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975321
1321418	Syvn1	synovial apoptosis inhibitor 1, synoviolin	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975321
1321418	Syvn1	synovial apoptosis inhibitor 1, synoviolin	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975321
1321420	Nxn	nucleoredoxin	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20160421	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20160421	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20160421	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20160421	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20201022	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20170504	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20200402	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001340	abnormal eyelid morphology		IEA		N	RGD:5509061	20160421	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20211021	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160421	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20241121	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20181227	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20160421	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20241121	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20160811	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0004666	absent stapedial artery		IEA		N	RGD:5509061	20170504	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20210128	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20201231	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20210520	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160804	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20190502	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20211021	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0010912	herniated liver		IEA		N	RGD:5509061	20170504	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16466971
1321420	Nxn	nucleoredoxin	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20970343
1321420	Nxn	nucleoredoxin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20160811	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20160811	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0013916	decreased intestine length		IEA		N	RGD:5509061	20170504	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1321420	Nxn	nucleoredoxin	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1321424	Grid2ip	glutamate receptor, ionotropic, delta 2 (Grid2) interacting protein 1	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509461
1321424	Grid2ip	glutamate receptor, ionotropic, delta 2 (Grid2) interacting protein 1	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509461
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210128	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210128	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1321430	Sugp1	SURP and G patch domain containing 1	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20220519	MGI			
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130660
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130660
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0002659	pituitary gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130660
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130660
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130660
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0009015	short proestrus		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0009047	short metestrus		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0009444	ovarian follicular cyst		IAGP		N	RGD:5509061	20220203	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0014589	abnormal gonadotropin-releasing hormone neuron morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0014592	decreased gonadotropin-releasing hormone neuron number		IAGP		N	RGD:5509061	20241212	MGI			PMID:21228153
1321432	Six6	sine oculis-related homeobox 6	gene	MP:0031436	decreased copulatory plug deposition		IAGP		N	RGD:5509061	20220922	MGI			PMID:21228153
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11284712
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11284712
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11284712
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11284712
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11284712
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11284712
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556917
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11284712
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16556917
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0004971	dermal hyperplasia		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11284712
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0010896	decreased lung compliance		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:29649548
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0012546	triangular face		IAGP		N	RGD:5509061	20141003	MGI			PMID:11284712
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1321434	Adamts2	ADAM metallopeptidase with thrombospondin type 1 motif 2	gene	MP:0031395	cutaneous mastocytosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29649548
1321436	Gtf2h2	general transcription factor II H, polypeptide 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000293	absent myocardial trabeculae		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:25625625
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160811	MGI			PMID:25625625
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522713
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448678
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448678
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448678
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448678
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20160811	MGI			PMID:25625625
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522713
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0005451	abnormal body composition		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20160811	MGI			PMID:25625625
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20160811	MGI			PMID:25625625
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0010565	absent fetal ductus arteriosus		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0010584	abnormal conotruncus septation		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20522713
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448678
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0012098	increased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23129809
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0012747	abnormal cardiac neural crest cell morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20160811	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20160811	MGI			PMID:25625625
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20171005	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0031554	abnormal aortic valve development		IAGP		N	RGD:5509061	20240125	MGI			PMID:26806701
1321438	Arid1a	AT-rich interaction domain 1A	gene	MP:0031555	abnormal pulmonary valve development		IAGP		N	RGD:5509061	20240125	MGI			PMID:26806701
1321440	Ankrd10	ankyrin repeat domain 10	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20260402	MGI			
1321440	Ankrd10	ankyrin repeat domain 10	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1321440	Ankrd10	ankyrin repeat domain 10	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321440	Ankrd10	ankyrin repeat domain 10	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1321442	Phlda3	pleckstrin homology like domain, family A, member 3	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032310
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770179
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0001391	abnormal tail movements		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0002944	increased lactate dehydrogenase level		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0003442	decreased circulating glycerol level		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0004917	abnormal T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770179
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770179
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770179
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20141003	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770179
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770179
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770179
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0008211	decreased mature B cell number		IEA		N	RGD:5509061	20160804	MGI			
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:14770179
1321445	Elk4	ETS transcription factor ELK4	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321447	Osbp2	oxysterol binding protein 2	gene	MP:0009852	increased Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20150205	MGI			PMID:24245814
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0009882	absent palatal shelf		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0010152	abnormal brain ependyma morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0011065	abnormal kidney epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0013214	decreased embryonic neuroepithelium primary cilium number		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20170202	MGI			PMID:26965371
1321452	Ccp110	centriolar coiled coil protein 110	gene	MP:0030320	abnormal temporal bone tympanic part morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26965371
1321454	Cfhr1	complement factor H-related 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20230601	MGI			
1321454	Cfhr1	complement factor H-related 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0012609	decreased complement C5 level		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0012610	increased complement C5 level		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321454	Cfhr1	complement factor H-related 1	gene	MP:0020217	increased circulating complement protein level		IAGP		N	RGD:5509061	20260122	MGI			PMID:32636836
1321455	Mybphl	myosin binding protein H-like	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0000520	absent kidney		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0003078	aphakia		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0003722	absent ureter		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0009495	abnormal common bile duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0009770	abnormal optic chiasm morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20150430	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0013186	abnormal basilar artery morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20171228	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1321455	Mybphl	myosin binding protein H-like	gene	MP:0014017	abnormal Wolffian duct connection		IEA		N	RGD:5509061	20170504	MGI			
1321456	Mpv17l	Mpv17 transgene, kidney disease mutant-like	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20220224	MGI			PMID:34883249
1321456	Mpv17l	Mpv17 transgene, kidney disease mutant-like	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20220224	MGI			PMID:34883249
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321459	Nubp1	nucleotide binding protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028652
1321462	Wtap	WT1 associating protein	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17644066
1321462	Wtap	WT1 associating protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17644066
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705179
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705179
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428452
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0000935	abnormal folding of telencephalic vesicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705179
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001705	abnormal proximal-distal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001784	abnormal fluid regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831469
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284942
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705179
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705179
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705179
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0003639	abnormal response to vitamins		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428452
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705179
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011192	decreased embryonic epiblast cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011525	abnormal placenta intervillous maternal lacunae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011529	increased placenta intervillous maternal lacunae size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0012258	philtrum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0012523	abnormal upper lip morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0013227	small brain ventricles		IAGP		N	RGD:5509061	20161103	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0020903	increased middle ear goblet cell number		IAGP		N	RGD:5509061	20191219	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20170921	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:17082251
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0030226	middle ear polyps		IAGP		N	RGD:5509061	20171019	MGI			PMID:23459932
1321464	Tgif1	TGFB-induced factor homeobox 1	gene	MP:0030410	middle ear effusion		IAGP		N	RGD:5509061	20191219	MGI			PMID:23459932
1321470	Ranbp1	RAN binding protein 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20190502	MGI			
1321470	Ranbp1	RAN binding protein 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20190502	MGI			
1321470	Ranbp1	RAN binding protein 1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20190502	MGI			
1321470	Ranbp1	RAN binding protein 1	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20190502	MGI			
1321470	Ranbp1	RAN binding protein 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310149
1321470	Ranbp1	RAN binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310149
1321470	Ranbp1	RAN binding protein 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1321470	Ranbp1	RAN binding protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310149
1321470	Ranbp1	RAN binding protein 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1321470	Ranbp1	RAN binding protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310149
1321470	Ranbp1	RAN binding protein 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20190502	MGI			
1321470	Ranbp1	RAN binding protein 1	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310149
1321470	Ranbp1	RAN binding protein 1	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310149
1321470	Ranbp1	RAN binding protein 1	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20221103	MGI			
1321470	Ranbp1	RAN binding protein 1	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321470	Ranbp1	RAN binding protein 1	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:25452572
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215345
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20170105	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20181227	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112872
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215345
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20181227	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20181227	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1321472	Scrib	scribbled planar cell polarity	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24095903
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:24095903
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:24095903
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20231207	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170105	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20150618	MGI			PMID:24276238
1321472	Scrib	scribbled planar cell polarity	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20170105	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112872
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11707073
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112872
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11707073
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24095903
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20170105	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003936	abnormal reproductive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112872
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112872
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20170105	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215345
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215345
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215345
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1321472	Scrib	scribbled planar cell polarity	gene	MP:0004961	increased prostate gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0005651	abnormal gonad rudiment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24095903
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20150618	MGI			PMID:24276238
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20150618	MGI			PMID:24276238
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11707073
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112872
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215345
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21515572
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0009770	abnormal optic chiasm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0010945	lung epithelium hyperplasia		IAGP		N	RGD:5509061	20150618	MGI			PMID:24276238
1321472	Scrib	scribbled planar cell polarity	gene	MP:0010975	abnormal lung lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1321472	Scrib	scribbled planar cell polarity	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112872
1321472	Scrib	scribbled planar cell polarity	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21965329
1321472	Scrib	scribbled planar cell polarity	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170105	MGI			
1321472	Scrib	scribbled planar cell polarity	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1321472	Scrib	scribbled planar cell polarity	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586490
1321472	Scrib	scribbled planar cell polarity	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586490
1321472	Scrib	scribbled planar cell polarity	gene	MP:0011964	increased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0012679	absent third ventricle		IAGP		N	RGD:5509061	20160915	MGI			PMID:10862153
1321472	Scrib	scribbled planar cell polarity	gene	MP:0013765	iris hyperplasia		IAGP		N	RGD:5509061	20150430	MGI			PMID:24095903
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0010998	pulmonary alveolar proteinosis		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0013772	increased effector memory T-helper cell number		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0031054	bronchiolitis		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321478	Copa	coatomer protein complex subunit alpha	gene	MP:0031238	reactive type II pneumocyte hyperplasia		IAGP		N	RGD:5509061	20220929	MGI			PMID:32198142
1321480	Ndn	necdin, MAGE family member	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11115855
1321480	Ndn	necdin, MAGE family member	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049186
1321480	Ndn	necdin, MAGE family member	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116257
1321480	Ndn	necdin, MAGE family member	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116257
1321480	Ndn	necdin, MAGE family member	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116257
1321480	Ndn	necdin, MAGE family member	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:11115855
1321480	Ndn	necdin, MAGE family member	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11115855
1321480	Ndn	necdin, MAGE family member	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508517
1321480	Ndn	necdin, MAGE family member	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11115855
1321480	Ndn	necdin, MAGE family member	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629158
1321480	Ndn	necdin, MAGE family member	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629158
1321480	Ndn	necdin, MAGE family member	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508517
1321480	Ndn	necdin, MAGE family member	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11115855
1321480	Ndn	necdin, MAGE family member	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629158
1321480	Ndn	necdin, MAGE family member	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049186
1321480	Ndn	necdin, MAGE family member	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508517
1321480	Ndn	necdin, MAGE family member	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10319852
1321480	Ndn	necdin, MAGE family member	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116257
1321480	Ndn	necdin, MAGE family member	gene	MP:0002321	hypoventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629158
1321480	Ndn	necdin, MAGE family member	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508517
1321480	Ndn	necdin, MAGE family member	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629158
1321480	Ndn	necdin, MAGE family member	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049186
1321480	Ndn	necdin, MAGE family member	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116257
1321480	Ndn	necdin, MAGE family member	gene	MP:0003880	abnormal central pattern generator function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629158
1321480	Ndn	necdin, MAGE family member	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116257
1321480	Ndn	necdin, MAGE family member	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508517
1321480	Ndn	necdin, MAGE family member	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116257
1321480	Ndn	necdin, MAGE family member	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629158
1321480	Ndn	necdin, MAGE family member	gene	MP:0006404	abnormal lumbar dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17116257
1321480	Ndn	necdin, MAGE family member	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508517
1321480	Ndn	necdin, MAGE family member	gene	MP:0010746	abnormal pre-Botzinger complex physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629158
1321480	Ndn	necdin, MAGE family member	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12629158
1321480	Ndn	necdin, MAGE family member	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11115855
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705627
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705627
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:14724135
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705627
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:14724135
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009233	enlarged sperm head		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705627
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:14724135
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009377	ectopic manchette		IAGP		N	RGD:5509061	20220210	MGI			PMID:14724135
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:14724135
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20141003	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:14724135
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0009839	multiflagellated sperm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705627
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0030980	abnormal acroplaxome morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:14724135
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20220303	MGI			PMID:11711676
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20220428	MGI			PMID:14724135
1321482	Agfg1	ArfGAP with FG repeats 1	gene	MP:0031682	abnormal centriole morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:15705627
1321484	Rhoj	ras homolog family member J	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20150122	MGI			PMID:24434213
1321484	Rhoj	ras homolog family member J	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20150122	MGI			PMID:24434213
1321484	Rhoj	ras homolog family member J	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535667
1321484	Rhoj	ras homolog family member J	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20150122	MGI			PMID:24434213
1321484	Rhoj	ras homolog family member J	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20150122	MGI			PMID:24434213
1321484	Rhoj	ras homolog family member J	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24434213
1321484	Rhoj	ras homolog family member J	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150122	MGI			PMID:24434213
1321484	Rhoj	ras homolog family member J	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20150122	MGI			PMID:24434213
1321484	Rhoj	ras homolog family member J	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20150122	MGI			PMID:24434213
1321486	Ap4b1	adaptor-related protein complex AP-4, beta 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18341993
1321486	Ap4b1	adaptor-related protein complex AP-4, beta 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18341993
1321487	Azi2	5-azacytidine induced gene 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610142
1321487	Azi2	5-azacytidine induced gene 2	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610142
1321487	Azi2	5-azacytidine induced gene 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610142
1321487	Azi2	5-azacytidine induced gene 2	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610142
1321487	Azi2	5-azacytidine induced gene 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610142
1321487	Azi2	5-azacytidine induced gene 2	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610142
1321489	Pank3	pantothenate kinase 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321489	Pank3	pantothenate kinase 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1321489	Pank3	pantothenate kinase 3	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1321489	Pank3	pantothenate kinase 3	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20221215	MGI			
1321489	Pank3	pantothenate kinase 3	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1321489	Pank3	pantothenate kinase 3	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1321489	Pank3	pantothenate kinase 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815849
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19111675
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20230119	MGI			
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19111675
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19111675
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19111675
1321495	Lpp	LIM domain containing preferred translocation partner in lipoma	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1321496	Zfp787	zinc finger protein 787	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1321496	Zfp787	zinc finger protein 787	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20220519	MGI			
1321496	Zfp787	zinc finger protein 787	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1321496	Zfp787	zinc finger protein 787	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1321496	Zfp787	zinc finger protein 787	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20220811	MGI			
1321496	Zfp787	zinc finger protein 787	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1321496	Zfp787	zinc finger protein 787	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1321496	Zfp787	zinc finger protein 787	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1321498	Ipo9	importin 9	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20210520	MGI			
1321498	Ipo9	importin 9	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1321498	Ipo9	importin 9	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1321498	Ipo9	importin 9	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20201022	MGI			
1321498	Ipo9	importin 9	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1321498	Ipo9	importin 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321498	Ipo9	importin 9	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1321501	Hoxc12	homeobox C12	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20201022	MGI			
1321501	Hoxc12	homeobox C12	gene	MP:0011999	abnormal tail length		IEA		N	RGD:5509061	20201022	MGI			
1321501	Hoxc12	homeobox C12	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1321502	Tmem115	transmembrane protein 115	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20250508	MGI			
1321502	Tmem115	transmembrane protein 115	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1321502	Tmem115	transmembrane protein 115	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20220519	MGI			
1321502	Tmem115	transmembrane protein 115	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1321502	Tmem115	transmembrane protein 115	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220519	MGI			
1321502	Tmem115	transmembrane protein 115	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0000267	abnormal heart development		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0000928	incomplete rostral neuropore closure		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210128	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0003400	kinked neural tube		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20151210	MGI			PMID:11929050
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0004180	failure of initiation of embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20151210	MGI			PMID:11929050
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20151210	MGI			PMID:11929050
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151210	MGI			PMID:11929050
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0012099	decreased spongiotrophoblast size		IEA		N	RGD:5509061	20251211	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1321507	Ppox	protoporphyrinogen oxidase	gene	MP:0014134	abnormal embryo morphology		IEA		N	RGD:5509061	20251211	MGI			
1321509	Plekhf1	pleckstrin homology and FYVE domain containing 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20191003	MGI			PMID:31189603
1321509	Plekhf1	pleckstrin homology and FYVE domain containing 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20191003	MGI			PMID:31189603
1321509	Plekhf1	pleckstrin homology and FYVE domain containing 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20191003	MGI			PMID:31189603
1321509	Plekhf1	pleckstrin homology and FYVE domain containing 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20191003	MGI			PMID:31189603
1321509	Plekhf1	pleckstrin homology and FYVE domain containing 1	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20191003	MGI			PMID:31189603
1321509	Plekhf1	pleckstrin homology and FYVE domain containing 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20191003	MGI			PMID:31189603
1321509	Plekhf1	pleckstrin homology and FYVE domain containing 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20191003	MGI			PMID:31189603
1321509	Plekhf1	pleckstrin homology and FYVE domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321509	Plekhf1	pleckstrin homology and FYVE domain containing 1	gene	MP:0030951	abnormal endocytosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:31189603
1321511	Rtp3	receptor transporter protein 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1321511	Rtp3	receptor transporter protein 3	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:2379821
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:3408670
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2379821
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0002551	abnormal blood coagulation		IEA		N	RGD:5509061	20111116	MGI			
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3408670
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12445206
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0005100	abnormal choroid pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11707070
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0005102	abnormal iris pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18715234
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11707070
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:3408670
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:3408670
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20170803	MGI			PMID:3408670
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20170803	MGI			PMID:3408670
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:3408670
1321514	Hps3	HPS3, biogenesis of lysosomal organelles complex 2 subunit 1	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:3408670
1321516	Cog4	component of oligomeric golgi complex 4	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200514	MGI			
1321516	Cog4	component of oligomeric golgi complex 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1321516	Cog4	component of oligomeric golgi complex 4	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1321516	Cog4	component of oligomeric golgi complex 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321516	Cog4	component of oligomeric golgi complex 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1321520	Tulp2	TUB like protein 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210520	MGI			
1321520	Tulp2	TUB like protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250320	MGI			PMID:40009443
1321520	Tulp2	TUB like protein 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20250320	MGI			PMID:40009443
1321520	Tulp2	TUB like protein 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20250320	MGI			PMID:40009443
1321520	Tulp2	TUB like protein 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1321520	Tulp2	TUB like protein 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20250320	MGI			PMID:40009443
1321520	Tulp2	TUB like protein 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:40009443
1321520	Tulp2	TUB like protein 2	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:40009443
1321520	Tulp2	TUB like protein 2	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210805	MGI			PMID:33763418
1321520	Tulp2	TUB like protein 2	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:40009443
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20160811	MGI			
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20160811	MGI			
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201231	MGI			
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114376
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160421	MGI			
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0004041	increased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20161201	MGI			PMID:25892012
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0004940	abnormal B-1 B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114376
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114376
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114376
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114376
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114376
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114376
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114376
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20161201	MGI			PMID:25892012
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1321524	Sema4d	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1321526	Prpf3	pre-mRNA processing factor 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321526	Prpf3	pre-mRNA processing factor 3	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811066
1321526	Prpf3	pre-mRNA processing factor 3	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811066
1321526	Prpf3	pre-mRNA processing factor 3	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811066
1321526	Prpf3	pre-mRNA processing factor 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18552388
1321526	Prpf3	pre-mRNA processing factor 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321526	Prpf3	pre-mRNA processing factor 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1321526	Prpf3	pre-mRNA processing factor 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591855
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17336907
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:17080428
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20190103	MGI			PMID:16651378
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15959515
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15959515
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897741
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12593800
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12593800
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581056
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001280	loss of vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12593800
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001664	abnormal digestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21168915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658279
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591855
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141225	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17336907
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22146645
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:21493891
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:28395734
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591855
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20240530	MGI			PMID:28395734
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20181122	MGI			PMID:21493891
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003246	loss of GABAergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003247	abnormal glutaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12593800
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581056
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20639863
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15959515
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220915	MGI			PMID:30213224
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004248	abnormal epaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:16651378
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004382	abnormal hair follicle melanogenesis		IAGP		N	RGD:5509061	20190103	MGI			PMID:16651378
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17229764
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004786	abnormal common cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21168915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591855
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21168915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658279
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12593800
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17984302
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12593800
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20181122	MGI			PMID:21493891
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20190103	MGI			PMID:16651378
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17336907
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20181227	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21168915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591855
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21168915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0006093	arteriovenous malformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581056
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21168915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15137944
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591855
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008137	absent podocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17229764
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12039915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008200	decreased follicular dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591855
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591855
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17658279
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009149	decreased pancreatic acinar cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009159	increased pancreatic acinar cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22146645
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009179	abnormal pancreatic alpha cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21168915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009408	decreased skeletal muscle fiber density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:16651378
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0010171	abnormal centroacinar cell of Langerhans morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22146645
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0010183	abnormal CD4-positive helper T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21168915
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0010198	decreased lymphatic vessel endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360386
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20181122	MGI			PMID:21493891
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0010942	abnormal respiratory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19502490
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011071	absent club cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19502490
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897741
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635610
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10476967
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17229764
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360386
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:17336907
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20181122	MGI			PMID:21493891
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0012023	decreased melanocyte number		IAGP		N	RGD:5509061	20190103	MGI			PMID:16651378
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0012099	decreased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15466160
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0021095	abnormal dorsal interneuron 4 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:18198335
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0031124	aortic valve inflammation		IAGP		N	RGD:5509061	20200917	MGI			PMID:21493891
1321530	Rbpj	recombination signal binding protein for immunoglobulin kappa J region	gene	MP:0031518	calcified aortic valve cusp		IAGP		N	RGD:5509061	20240118	MGI			PMID:21493891
1321540	Ccl9	C-C motif chemokine ligand 9	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1321540	Ccl9	C-C motif chemokine ligand 9	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1321542	Plxnb1	plexin B1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1321542	Plxnb1	plexin B1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17519029
1321542	Plxnb1	plexin B1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18799546
1321542	Plxnb1	plexin B1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1321542	Plxnb1	plexin B1	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1321542	Plxnb1	plexin B1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0006097	abnormal cerebellar lobule formation		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321542	Plxnb1	plexin B1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1321542	Plxnb1	plexin B1	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20161201	MGI			PMID:25892012
1321542	Plxnb1	plexin B1	gene	MP:0010981	abnormal branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18799546
1321542	Plxnb1	plexin B1	gene	MP:0010981	abnormal branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1321542	Plxnb1	plexin B1	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18799546
1321542	Plxnb1	plexin B1	gene	MP:0011761	abnormal ureteric bud trunk morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:21035938
1321542	Plxnb1	plexin B1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20161222	MGI			PMID:26579598
1321546	Tmem17	transmembrane protein 17	gene	MP:0001491	unresponsive to tactile stimuli		IEA		N	RGD:5509061	20240523	MGI			
1321546	Tmem17	transmembrane protein 17	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1321546	Tmem17	transmembrane protein 17	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20240523	MGI			
1321546	Tmem17	transmembrane protein 17	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1321546	Tmem17	transmembrane protein 17	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1321548	Dgcr2	DiGeorge syndrome critical region gene 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1321548	Dgcr2	DiGeorge syndrome critical region gene 2	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20201231	MGI			
1321548	Dgcr2	DiGeorge syndrome critical region gene 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20230601	MGI			
1321548	Dgcr2	DiGeorge syndrome critical region gene 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20210128	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20241121	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20240523	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
1321555	Tpgs2	tubulin polyglutamylase complex subunit 2	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1321556	Mgat4d	MGAT4 family, member D	gene	MP:0000467	abnormal esophagus morphology		IEA		N	RGD:5509061	20161201	MGI			
1321556	Mgat4d	MGAT4 family, member D	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20161201	MGI			
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0000962	disorganized dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12139926
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643673
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643673
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0002917	decreased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:8643673
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12139926
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1321559	Prkacb	protein kinase, cAMP dependent, catalytic, beta	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1321561	Ch25h	cholesterol 25-hydroxylase	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20181227	MGI			
1321561	Ch25h	cholesterol 25-hydroxylase	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1321561	Ch25h	cholesterol 25-hydroxylase	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1321561	Ch25h	cholesterol 25-hydroxylase	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805370
1321561	Ch25h	cholesterol 25-hydroxylase	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805370
1321561	Ch25h	cholesterol 25-hydroxylase	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805370
1321561	Ch25h	cholesterol 25-hydroxylase	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805370
1321564	Vmn2r81	vomeronasal 2, receptor 81	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21112400
1321564	Vmn2r81	vomeronasal 2, receptor 81	gene	MP:0002243	abnormal vomeronasal organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21112400
1321564	Vmn2r81	vomeronasal 2, receptor 81	gene	MP:0011678	abnormal vomeronasal sensory neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24719092
1321564	Vmn2r81	vomeronasal 2, receptor 81	gene	MP:0011679	abnormal vomeronasal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24719092
1321566	Cdr2	cerebellar degeneration-related 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111215	MGI			
1321570	B3gnt7	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1321570	B3gnt7	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1321570	B3gnt7	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:29625490
1321570	B3gnt7	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20231207	MGI			
1321570	B3gnt7	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	gene	MP:0003092	decreased cornea stroma thickness		IAGP		N	RGD:5509061	20180628	MGI			PMID:29625490
1321570	B3gnt7	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20180628	MGI			PMID:29625490
1321572	Nptx1	neuronal pentraxin 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16763034
1321572	Nptx1	neuronal pentraxin 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16763034
1321574	Tekt3	tektin 3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18951373
1321574	Tekt3	tektin 3	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18951373
1321574	Tekt3	tektin 3	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18951373
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20180426	MGI			PMID:28287403
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809760
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809760
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20160421	MGI			
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809760
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20180426	MGI			PMID:28287403
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0003865	lymph node inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20180426	MGI			PMID:28287403
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809760
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0005190	osteomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20180426	MGI			PMID:28287403
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008704	abnormal interleukin-6 secretion		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283041
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20180426	MGI			PMID:28287403
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20180426	MGI			PMID:28287403
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20180426	MGI			PMID:28287403
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0013123	head/neck swellings		IAGP		N	RGD:5509061	20160128	MGI			PMID:25705883
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0014450	increased circulating enzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0030466	alveolar process atrophy		IAGP		N	RGD:5509061	20171221	MGI			PMID:17218256
1321584	Sh3bp2	SH3-domain binding protein 2	gene	MP:0030987	spinal cord inflammation		IAGP		N	RGD:5509061	20191128	MGI			PMID:17218256
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018287
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018287
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10499589
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018287
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018287
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0003234	enhanced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018287
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018287
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0004524	short cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1321588	Eps8	epidermal growth factor receptor pathway substrate 8	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018287
1321590	Ints8	integrator complex subunit 8	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1321590	Ints8	integrator complex subunit 8	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1321590	Ints8	integrator complex subunit 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1321590	Ints8	integrator complex subunit 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20230330	MGI			PMID:35478358
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201231	MGI			
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20230330	MGI			PMID:35478358
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:35478358
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20250508	MGI			
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1321594	Pla2g4e	phospholipase A2, group IVE	gene	MP:0012572	increased susceptibility to chemically induced skin inflammation		IAGP		N	RGD:5509061	20230330	MGI			PMID:35478358
1321598	Ms4a3	membrane-spanning 4-domains, subfamily A, member 3	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428451
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009599
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428451
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009599
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20230824	MGI			PMID:12897131
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12727892
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428451
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16009599
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428451
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0012121	sclerocornea		IEA		N	RGD:5509061	20190502	MGI			
1321601	Rad54l	RAD54 like (S. cerevisiae)	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20230824	MGI			PMID:12897131
1321608	Slc27a3	solute carrier family 27 (fatty acid transporter), member 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1321608	Slc27a3	solute carrier family 27 (fatty acid transporter), member 3	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20240523	MGI			
1321608	Slc27a3	solute carrier family 27 (fatty acid transporter), member 3	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1321608	Slc27a3	solute carrier family 27 (fatty acid transporter), member 3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20211021	MGI			
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20240229	MGI			PMID:34994051
1321609	Ergic2	ERGIC and golgi 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1321611	Rpl26	ribosomal protein L26	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20251106	MGI			PMID:40347470
1321611	Rpl26	ribosomal protein L26	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20251106	MGI			PMID:40347470
1321611	Rpl26	ribosomal protein L26	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20251106	MGI			PMID:40347470
1321611	Rpl26	ribosomal protein L26	gene	MP:0005370	liver/biliary system phenotype		IAGP		N	RGD:5509061	20251106	MGI			PMID:40347470
1321611	Rpl26	ribosomal protein L26	gene	MP:0010087	increased circulating fructosamine level		IAGP		N	RGD:5509061	20251106	MGI			PMID:40347470
1321611	Rpl26	ribosomal protein L26	gene	MP:0014242	abnormal ribosome biogenesis		IAGP		N	RGD:5509061	20251106	MGI			PMID:40347470
1321611	Rpl26	ribosomal protein L26	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20251106	MGI			PMID:40347470
1321616	Anp32e	acidic nuclear phosphoprotein 32 family member E	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844742
1321616	Anp32e	acidic nuclear phosphoprotein 32 family member E	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20844742
1321616	Anp32e	acidic nuclear phosphoprotein 32 family member E	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21049064
1321616	Anp32e	acidic nuclear phosphoprotein 32 family member E	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636789
1321616	Anp32e	acidic nuclear phosphoprotein 32 family member E	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636789
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0031265	increased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321619	Creld2	cysteine-rich with EGF-like domains 2	gene	MP:0031271	increased susceptibility to age-related hepatic steatosis		IAGP		N	RGD:5509061	20230511	MGI			PMID:34549824
1321621	Mccc1	methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200402	MGI			
1321621	Mccc1	methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
1321621	Mccc1	methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321621	Mccc1	methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1321621	Mccc1	methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201231	MGI			
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20191107	MGI			PMID:29228266
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191107	MGI			PMID:29228266
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20211021	MGI			
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20240523	MGI			
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20191107	MGI			PMID:29228266
1321624	Aars2	alanyl-tRNA synthetase 2, mitochondrial	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20180712	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20180712	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20180712	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220428	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20220428	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0013410	decreased dendritic epidermal T cell number		IEA		N	RGD:5509061	20201231	MGI			
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:28008940
1321626	Mkrn2	makorin, ring finger protein, 2	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:28008940
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0000035	abnormal membranous labyrinth morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0001983	abnormal olfactory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028982
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0002985	abnormal urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174750
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0002986	decreased urine calcium level		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174750
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174750
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174750
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0003144	decreased otolith number		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0003462	abnormal response to novel odor		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028982
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0004043	abnormal pH regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028982
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0004287	abnormal spiral limbus morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0004292	abnormal spiral ligament fibrocyte morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0004293	abnormal type I spiral ligament fibrocytes		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0004295	abnormal type III spiral ligament fibrocytes		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0004862	small scala tympani		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0004863	thin spiral ligament		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0006021	abnormal Reissner membrane morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0006403	abnormal cochlear endolymph ionic homeostasis		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0008309	dilated scala media		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174750
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0011417	abnormal renal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:16174750
1321628	Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20171012	MGI			PMID:28934385
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0001985	abnormal gustatory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12581520
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12581520
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16355226
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19244541
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758465
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0004209	abnormal sweet taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12581520
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0004209	abnormal sweet taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16355226
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0004210	abnormal bitter taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12581520
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0004210	abnormal bitter taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16355226
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0004211	abnormal sour taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16355226
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0004212	abnormal salty taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16355226
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0004213	abnormal umami taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15738181
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0004213	abnormal umami taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16355226
1321630	Trpm5	transient receptor potential cation channel, subfamily M, member 5	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758465
1321632	Sorcs2	sortilin-related VPS10 domain containing receptor 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:24908487
1321632	Sorcs2	sortilin-related VPS10 domain containing receptor 2	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20150903	MGI			PMID:24908487
1321632	Sorcs2	sortilin-related VPS10 domain containing receptor 2	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:24908487
1321632	Sorcs2	sortilin-related VPS10 domain containing receptor 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20150903	MGI			PMID:24908487
1321632	Sorcs2	sortilin-related VPS10 domain containing receptor 2	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20150903	MGI			PMID:24908487
1321632	Sorcs2	sortilin-related VPS10 domain containing receptor 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20150903	MGI			PMID:24908487
1321632	Sorcs2	sortilin-related VPS10 domain containing receptor 2	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:24908487
1321632	Sorcs2	sortilin-related VPS10 domain containing receptor 2	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20150903	MGI			PMID:24908487
1321632	Sorcs2	sortilin-related VPS10 domain containing receptor 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:24908487
1321638	Apoh	apolipoprotein H	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145969
1321638	Apoh	apolipoprotein H	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11145969
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11051546
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11051546
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:26601902
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20151224	MGI			PMID:26601902
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0002238	abnormal nasal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0002388	abnormal Peyer's patch epithelium morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:25751305
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0002388	abnormal Peyer's patch epithelium morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:26601902
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:26601902
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:26601902
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:26601902
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20161013	MGI			PMID:26659571
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0004918	abnormal negative T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502664
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11051546
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15355564
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20151224	MGI			PMID:26601902
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10500098
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502664
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11051546
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940926
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0021030	decreased tumor necrosis factor (ligand) superfamily member 11 level		IAGP		N	RGD:5509061	20230202	MGI			PMID:33724536
1321640	Tnfrsf11a	tumor necrosis factor receptor superfamily, member 11a, NFKB activator	gene	MP:0030505	tooth impaction		IAGP		N	RGD:5509061	20191219	MGI			PMID:10500098
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571110
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22399681
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571110
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0001075	abnormal accessory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571110
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0001075	abnormal accessory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22399681
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079460
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079460
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0004568	fusion of glossopharyngeal and vagus nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571110
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0004949	absent neuronal precursor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571110
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571110
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0005488	bronchial epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079460
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079460
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0010942	abnormal respiratory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079460
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0010943	abnormal bronchus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079460
1321644	Nkx2-9	NK2 homeobox 9	gene	MP:0014747	abnormal motor neuron axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:16267219
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20170119	MGI			PMID:27671873
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170119	MGI			PMID:27671873
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20170119	MGI			PMID:27671873
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282322
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632607
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282322
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27671873
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632607
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632607
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27671873
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20170119	MGI			PMID:27671873
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632607
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20181227	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20170119	MGI			PMID:27671873
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18632607
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282322
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0011256	abnormal neural fold morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27671873
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1321650	Rad9a	RAD9 checkpoint clamp component A	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1321652	Upk3a	uroplakin 3A	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085999
1321652	Upk3a	uroplakin 3A	gene	MP:0001948	vesicoureteral reflux		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085999
1321652	Upk3a	uroplakin 3A	gene	MP:0003630	abnormal urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085999
1321652	Upk3a	uroplakin 3A	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085999
1321652	Upk3a	uroplakin 3A	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085999
1321652	Upk3a	uroplakin 3A	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085999
1321652	Upk3a	uroplakin 3A	gene	MP:0010386	abnormal urinary bladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085999
1321652	Upk3a	uroplakin 3A	gene	MP:0011535	increased urination frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085999
1321652	Upk3a	uroplakin 3A	gene	MP:0011783	abnormal ureteral orifice morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085999
1321656	Zfp7	zinc finger protein 7	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1321656	Zfp7	zinc finger protein 7	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1321660	Entpd7	ectonucleoside triphosphate diphosphohydrolase 7	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23241884
1321660	Entpd7	ectonucleoside triphosphate diphosphohydrolase 7	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23241884
1321660	Entpd7	ectonucleoside triphosphate diphosphohydrolase 7	gene	MP:0008073	abnormal CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23241884
1321660	Entpd7	ectonucleoside triphosphate diphosphohydrolase 7	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23241884
1321660	Entpd7	ectonucleoside triphosphate diphosphohydrolase 7	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23241884
1321662	Ccna1	cyclin A1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047941
1321662	Ccna1	cyclin A1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220623	MGI			PMID:9843212
1321662	Ccna1	cyclin A1	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047941
1321662	Ccna1	cyclin A1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047941
1321662	Ccna1	cyclin A1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843212
1321662	Ccna1	cyclin A1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047941
1321662	Ccna1	cyclin A1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15047941
1321662	Ccna1	cyclin A1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843212
1321662	Ccna1	cyclin A1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9843212
1321662	Ccna1	cyclin A1	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1321662	Ccna1	cyclin A1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:9843212
1321662	Ccna1	cyclin A1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:15047941
1321662	Ccna1	cyclin A1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:9843212
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20190502	MGI			
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0002958	cerebral aqueductal stenosis		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0010752	impaired mucociliary clearance		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0013228	brain ventricle stenosis		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0030316	enlarged neurocranium		IAGP		N	RGD:5509061	20201029	MGI			PMID:32376681
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0031352	absent sperm axonemal central pair		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:34255152
1321666	Cfap206	cilia and flagella associated protein 206	gene	MP:0031438	abnormal sperm radial spoke morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32376681
1321671	Cul2	cullin 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321671	Cul2	cullin 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0021160	decreased heart right ventricle wall thickness		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20230914	MGI			PMID:37233188
1321685	Rtf1	RTF1, Paf1/RNA polymerase II complex component	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:37233188
1321691	Kctd3	potassium channel tetramerisation domain containing 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210826	MGI			
1321691	Kctd3	potassium channel tetramerisation domain containing 3	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210826	MGI			
1321691	Kctd3	potassium channel tetramerisation domain containing 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1321691	Kctd3	potassium channel tetramerisation domain containing 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1321691	Kctd3	potassium channel tetramerisation domain containing 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1321691	Kctd3	potassium channel tetramerisation domain containing 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0020867	increased lipogenesis		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321694	Ppdpf	pancreatic progenitor cell differentiation and proliferation factor	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210826	MGI			PMID:34031390
1321700	Tpr	translocated promoter region, nuclear basket protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20230601	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:25272040
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20200102	MGI			PMID:25272040
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20150430	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20150430	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20200402	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20250508	MGI			
1321707	Afap1l2	actin filament associated protein 1-like 2	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1321708	Cwc15	CWC15 spliceosome-associated protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1321709	Iqch	IQ motif containing H	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1321709	Iqch	IQ motif containing H	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1321709	Iqch	IQ motif containing H	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20240425	MGI			PMID:36975404
1321709	Iqch	IQ motif containing H	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321711	Rmi1	RecQ mediated genome instability 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:20050919
1321713	Arhgef3	Rho guanine nucleotide exchange factor 3	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20170720	MGI			PMID:28542600
1321713	Arhgef3	Rho guanine nucleotide exchange factor 3	gene	MP:0005397	hematopoietic system phenotype		IAGP		N	RGD:5509061	20201231	MGI			PMID:28542600
1321713	Arhgef3	Rho guanine nucleotide exchange factor 3	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20170720	MGI			PMID:28542600
1321713	Arhgef3	Rho guanine nucleotide exchange factor 3	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20210610	MGI			PMID:33406419
1321713	Arhgef3	Rho guanine nucleotide exchange factor 3	gene	MP:0013161	enhanced muscle regeneration		IAGP		N	RGD:5509061	20210610	MGI			PMID:33406419
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:22674806
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170209	MGI			PMID:22674806
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20170209	MGI			PMID:22674806
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:22674806
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:24440599
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:22674806
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:24440599
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:15951813
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16688530
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20170209	MGI			PMID:22674806
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:7621074
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20170209	MGI			PMID:18245664
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:17936561
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008618	decreased circulating interleukin-12 level		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20457904
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20170209	MGI			PMID:22674806
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0011815	increased pre-pro B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:24255108
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20230119	MGI			
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16688530
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16688530
1321715	Flt3	FMS-like tyrosine kinase 3	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:20457904
1321716	Smpd4	sphingomyelin phosphodiesterase 4	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1321716	Smpd4	sphingomyelin phosphodiesterase 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20170504	MGI			
1321716	Smpd4	sphingomyelin phosphodiesterase 4	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170504	MGI			
1321716	Smpd4	sphingomyelin phosphodiesterase 4	gene	MP:0003586	dilated ureter		IEA		N	RGD:5509061	20170504	MGI			
1321716	Smpd4	sphingomyelin phosphodiesterase 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321716	Smpd4	sphingomyelin phosphodiesterase 4	gene	MP:0011513	abnormal vertebral artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1321717	Ropn1	ropporin, rhophilin associated protein 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021175
1321717	Ropn1	ropporin, rhophilin associated protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021175
1321717	Ropn1	ropporin, rhophilin associated protein 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021175
1321717	Ropn1	ropporin, rhophilin associated protein 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22021175
1321717	Ropn1	ropporin, rhophilin associated protein 1	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:22021175
1321719	Togaram2	TOG array regulator of axonemal microtubules 2	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20250508	MGI			
1321721	Cldn15	claudin 15	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0000481	abnormal enterocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0009483	enlarged ileum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20150618	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0011882	enlarged duodenum		IAGP		N	RGD:5509061	20150618	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0013796	abnormal duodenal goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:18242218
1321721	Cldn15	claudin 15	gene	MP:0013798	abnormal jejunal goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:18242218
1321723	Foxs1	forkhead box S1	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964817
1321723	Foxs1	forkhead box S1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964817
1321723	Foxs1	forkhead box S1	gene	MP:0009489	abnormal blood vessel endothelium morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:18288644
1321723	Foxs1	forkhead box S1	gene	MP:0031138	testicular hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:18288644
1321724	Tmem151a	transmembrane protein 151A	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20240912	MGI			PMID:34518509
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0008291	abnormal adrenocortical cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0008579	abnormal Purkinje cell differentiation		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0012217	increased plasmalogen level		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0012218	decreased brain plasmalogen level		IAGP		N	RGD:5509061	20150528	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0014010	abnormal peroxisome morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0014967	increased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:20959636
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0020847	abnormal peroxisome physiology		IAGP		N	RGD:5509061	20230615	MGI			PMID:12897163
1321727	Pex13	peroxisomal biogenesis factor 13	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:12897163
1321728	Ccnyl1	cyclin Y-like 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20151008	MGI			PMID:26305884
1321728	Ccnyl1	cyclin Y-like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20151008	MGI			PMID:26305884
1321728	Ccnyl1	cyclin Y-like 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20151008	MGI			PMID:26305884
1321728	Ccnyl1	cyclin Y-like 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20151008	MGI			PMID:26305884
1321728	Ccnyl1	cyclin Y-like 1	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20151008	MGI			PMID:26305884
1321728	Ccnyl1	cyclin Y-like 1	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:26305884
1321728	Ccnyl1	cyclin Y-like 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20151008	MGI			PMID:26305884
1321728	Ccnyl1	cyclin Y-like 1	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:26305884
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0002879	increased cellular sensitivity to X-ray irradiation induced cell death		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0003214	neurofibrillary tangles		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0003927	increased cellular glucose import		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0013243	abnormal carbohydrate metabolism		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0014345	abnormal neuron mitochondrial morphology		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321730	Immt	inner membrane protein, mitochondrial	gene	MP:0020083	decreased hippocampus volume		IAGP		N	RGD:5509061	20240222	MGI			PMID:36974636
1321733	Cdip1	cell death inducing Trp53 target 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1321733	Cdip1	cell death inducing Trp53 target 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20181227	MGI			
1321733	Cdip1	cell death inducing Trp53 target 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20190418	MGI			PMID:24139803
1321733	Cdip1	cell death inducing Trp53 target 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321733	Cdip1	cell death inducing Trp53 target 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1321735	Elf3	E74-like factor 3	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984530
1321735	Elf3	E74-like factor 3	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984530
1321735	Elf3	E74-like factor 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984530
1321735	Elf3	E74-like factor 3	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984530
1321735	Elf3	E74-like factor 3	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984530
1321735	Elf3	E74-like factor 3	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984530
1321735	Elf3	E74-like factor 3	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984530
1321735	Elf3	E74-like factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984530
1321735	Elf3	E74-like factor 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984530
1321735	Elf3	E74-like factor 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0001876	decreased inflammatory response		IEA		N	RGD:5509061	20220811	MGI			
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0003880	abnormal central pattern generator function		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0004557	dilated allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0004712	notochord degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0008503	abnormal spinal cord grey matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093944
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808099
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0011856	abnormal glomerular filtration barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525419
1321737	Nck1	non-catalytic region of tyrosine kinase adaptor protein 1	gene	MP:0020100	decreased susceptibility to diet-induced aortic fatty streak lesions		IEA		N	RGD:5509061	20220811	MGI			
1321739	Msh6	mutS homolog 6	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15324697
1321739	Msh6	mutS homolog 6	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390556
1321739	Msh6	mutS homolog 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706084
1321739	Msh6	mutS homolog 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390556
1321739	Msh6	mutS homolog 6	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15324697
1321739	Msh6	mutS homolog 6	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20180215	MGI			
1321739	Msh6	mutS homolog 6	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706084
1321739	Msh6	mutS homolog 6	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15324697
1321739	Msh6	mutS homolog 6	gene	MP:0009222	increased uterus tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545954
1321739	Msh6	mutS homolog 6	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545954
1321739	Msh6	mutS homolog 6	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706084
1321739	Msh6	mutS homolog 6	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390556
1321739	Msh6	mutS homolog 6	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545954
1321739	Msh6	mutS homolog 6	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545954
1321739	Msh6	mutS homolog 6	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545954
1321739	Msh6	mutS homolog 6	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706084
1321739	Msh6	mutS homolog 6	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15324697
1321739	Msh6	mutS homolog 6	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9390556
1321739	Msh6	mutS homolog 6	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:10545954
1321739	Msh6	mutS homolog 6	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:15324697
1321739	Msh6	mutS homolog 6	gene	MP:0014766	impaired mismatch repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:10706084
1321741	U2af2	U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20220519	MGI			
1321741	U2af2	U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1321741	U2af2	U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1321741	U2af2	U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20240926	MGI			
1321741	U2af2	U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20230601	MGI			
1321741	U2af2	U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1321741	U2af2	U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1321741	U2af2	U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1321744	Galnt2	polypeptide N-acetylgalactosaminyltransferase 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20191114	MGI			PMID:27508872
1321744	Galnt2	polypeptide N-acetylgalactosaminyltransferase 2	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20191114	MGI			PMID:27508872
1321744	Galnt2	polypeptide N-acetylgalactosaminyltransferase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1321744	Galnt2	polypeptide N-acetylgalactosaminyltransferase 2	gene	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20191114	MGI			PMID:27508872
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0001872	sinus inflammation		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20221215	MGI			
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20221215	MGI			
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0010152	abnormal brain ependyma morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0010160	increased oligodendrocyte number		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0013907	abnormal cerebrospinal fluid flow		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321746	Rsph9	radial spoke head 9 homolog (Chlamydomonas)	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20201029	MGI			PMID:32709945
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736371
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736371
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736371
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20151126	MGI			PMID:23773267
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201022	MGI			
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20211021	MGI			
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0004478	increased testicular teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0004478	increased testicular teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:4692863
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20151126	MGI			PMID:23773267
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20151126	MGI			PMID:23773267
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736371
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:3860691
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20151126	MGI			PMID:23773267
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20211021	MGI			
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151126	MGI			PMID:23773267
1321749	Dnd1	DND microRNA-mediated repression inhibitor 1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151126	MGI			PMID:23773267
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20170413	MGI			
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0001790	abnormal immune system physiology		IEA		N	RGD:5509061	20170413	MGI			
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20190822	MGI			PMID:28285769
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20170413	MGI			
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20190822	MGI			PMID:28285769
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0009642	abnormal blood homeostasis		IEA		N	RGD:5509061	20170413	MGI			
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0010865	prenatal growth retardation		IEA		N	RGD:5509061	20170413	MGI			
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20190822	MGI			PMID:28285769
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20190822	MGI			PMID:28285769
1321753	Cwc27	CWC27 spliceosome-associated protein	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20190822	MGI			PMID:28285769
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26494538
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0004035	abnormal sublingual gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009145	abnormal pancreatic acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009149	decreased pancreatic acinar cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009154	pancreatic acinar hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009162	absent pancreatic acinar cell zymogen granule		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009165	abnormal endocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0010148	abnormal exocrine pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170202	MGI			PMID:26494538
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0011932	abnormal endocrine pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0013568	gastric gland degeneration		IAGP		N	RGD:5509061	20150305	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0013581	nasal gland degeneration		IAGP		N	RGD:5509061	20150305	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0013583	salivary gland degeneration		IAGP		N	RGD:5509061	20150312	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0013584	pancreas degeneration		IAGP		N	RGD:5509061	20150312	MGI			PMID:22745161
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:26494538
1321757	Sec23b	SEC23 homolog B, COPII coat complex component	gene	MP:0014260	embryonic lethality prior to organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:26494538
1321759	Alg1	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1321759	Alg1	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170105	MGI			
1321759	Alg1	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321759	Alg1	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321759	Alg1	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1321759	Alg1	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20211021	MGI			
1321759	Alg1	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321761	Kdm1b	lysine (K)-specific demethylase 1B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19727073
1321761	Kdm1b	lysine (K)-specific demethylase 1B	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19727073
1321767	Gpank1	G patch domain and ankyrin repeats 1	gene	MP:0005575	increased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1321767	Gpank1	G patch domain and ankyrin repeats 1	gene	MP:0005585	increased tidal volume		IEA		N	RGD:5509061	20201022	MGI			
1321770	Cic	capicua transcriptional repressor	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20201002	MGI			PMID:32229723
1321770	Cic	capicua transcriptional repressor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
1321770	Cic	capicua transcriptional repressor	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201002	MGI			PMID:32229723
1321770	Cic	capicua transcriptional repressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22053053
1321770	Cic	capicua transcriptional repressor	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20201002	MGI			PMID:32229723
1321770	Cic	capicua transcriptional repressor	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
1321770	Cic	capicua transcriptional repressor	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22053053
1321770	Cic	capicua transcriptional repressor	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20201002	MGI			PMID:32229723
1321770	Cic	capicua transcriptional repressor	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20201002	MGI			PMID:32229723
1321770	Cic	capicua transcriptional repressor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014525
1321770	Cic	capicua transcriptional repressor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20201002	MGI			PMID:32229723
1321770	Cic	capicua transcriptional repressor	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0020337	abnormal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0020594	decreased cerebral cortex cell number		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1321770	Cic	capicua transcriptional repressor	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:28288114
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000256	echinocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1321772	Diaph1	diaphanous related formin 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1321772	Diaph1	diaphanous related formin 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682067
1321772	Diaph1	diaphanous related formin 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1321772	Diaph1	diaphanous related formin 1	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682067
1321772	Diaph1	diaphanous related formin 1	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20250508	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0004978	decreased B-1 B cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682067
1321772	Diaph1	diaphanous related formin 1	gene	MP:0005046	absent spleen white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699759
1321772	Diaph1	diaphanous related formin 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682067
1321772	Diaph1	diaphanous related formin 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1321772	Diaph1	diaphanous related formin 1	gene	MP:0008073	abnormal CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682067
1321772	Diaph1	diaphanous related formin 1	gene	MP:0008077	abnormal CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682067
1321772	Diaph1	diaphanous related formin 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682067
1321772	Diaph1	diaphanous related formin 1	gene	MP:0009949	abnormal olfactory bulb granule cell layer morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1321772	Diaph1	diaphanous related formin 1	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0010839	decreased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1321772	Diaph1	diaphanous related formin 1	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IEA		N	RGD:5509061	20200514	MGI			
1321776	Ccdc77	coiled-coil domain containing 77	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321778	Acap3	ArfGAP with coiled-coil, ankyrin repeat and PH domains 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20141003	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0009806	abnormal otic vesicle morphology		IEA		N	RGD:5509061	20250508	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1321779	Emsy	EMSY, BRCA2-interacting transcriptional repressor	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1321783	Cbx1	chromobox 1	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141003	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20250508	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20221215	MGI			
1321783	Cbx1	chromobox 1	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20250508	MGI			
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477466
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23223571
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0003596	epididymis inflammation		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0004614	caudal vertebral transformation		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23223571
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0008805	decreased circulating amylase level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0009161	pancreatic acinar cell zymogen granule accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18477466
1321785	Sytl1	synaptotagmin-like 1	gene	MP:0031110	meningitis		IAGP		N	RGD:5509061	20200910	MGI			PMID:24652767
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16551741
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17549747
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:17549747
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16551741
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:16551741
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:16551741
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18941222
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18941222
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:18941222
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17549747
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20200310	MGI			PMID:18941222
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20231214	MGI			PMID:37862170
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20937851
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20231214	MGI			PMID:37862170
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0009080	uterus inflammation		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0010050	hypermyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11395000
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20231214	MGI			PMID:37862170
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0014329	abnormal Purkinje cell axon morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:16551741
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0014329	abnormal Purkinje cell axon morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:17549747
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0014587	impaired fine motor coordination		IAGP		N	RGD:5509061	20241219	MGI			PMID:37862170
1321787	Ccr10	C-C motif chemokine receptor 10	gene	MP:0020212	impaired leukocyte migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:35663027
1321792	Klra17	killer cell lectin-like receptor, subfamily A, member 17	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075287
1321792	Klra17	killer cell lectin-like receptor, subfamily A, member 17	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075287
1321792	Klra17	killer cell lectin-like receptor, subfamily A, member 17	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075287
1321792	Klra17	killer cell lectin-like receptor, subfamily A, member 17	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075287
1321792	Klra17	killer cell lectin-like receptor, subfamily A, member 17	gene	MP:0008618	decreased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075287
1321792	Klra17	killer cell lectin-like receptor, subfamily A, member 17	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075287
1321792	Klra17	killer cell lectin-like receptor, subfamily A, member 17	gene	MP:0008769	abnormal plasmacytoid dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075287
1321792	Klra17	killer cell lectin-like receptor, subfamily A, member 17	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:19075287
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201231	MGI			
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20190502	MGI			
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20200310	MGI			PMID:29371327
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:29371327
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20200310	MGI			PMID:29371327
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29371327
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29371327
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321794	Fmc1	formation of mitochondrial complex V assembly factor 1	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:29371327
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20241121	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241003	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230601	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0002718	abnormal inner cell mass morphology		IEA		N	RGD:5509061	20241003	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1321796	Dhx8	DEAH-box helicase 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1321798	Tmem176a	transmembrane protein 176A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1321798	Tmem176a	transmembrane protein 176A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
1321798	Tmem176a	transmembrane protein 176A	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1321798	Tmem176a	transmembrane protein 176A	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1321798	Tmem176a	transmembrane protein 176A	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20250508	MGI			
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0006323	abnormal extraembryonic mesoderm development		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321806	Rbm14	RNA binding motif protein 14	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20201001	MGI			PMID:31794640
1321809	Mlph	melanophilin	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:11504925
1321809	Mlph	melanophilin	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247639
1321809	Mlph	melanophilin	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410303
1321809	Mlph	melanophilin	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713933
1321809	Mlph	melanophilin	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:5726144
1321809	Mlph	melanophilin	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247639
1321809	Mlph	melanophilin	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:5726144
1321809	Mlph	melanophilin	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5726144
1321809	Mlph	melanophilin	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247639
1321809	Mlph	melanophilin	gene	MP:0005607	decreased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1321809	Mlph	melanophilin	gene	MP:0008733	abnormal hair shaft melanin granule distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:17247639
1321809	Mlph	melanophilin	gene	MP:0009555	abnormal hair follicle melanin granule distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
1321809	Mlph	melanophilin	gene	MP:0010193	abnormal choroid melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4634048
1321811	Pla2g7	phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20160225	MGI			PMID:20531249
1321811	Pla2g7	phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1321811	Pla2g7	phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1321811	Pla2g7	phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20240523	MGI			
1321811	Pla2g7	phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20170622	MGI			PMID:20531249
1321813	Trmt10b	tRNA methyltransferase 10B	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20220811	MGI			
1321813	Trmt10b	tRNA methyltransferase 10B	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1321816	Ndufb3	NADH:ubiquinone oxidoreductase subunit B3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1321820	Lipg	lipase G, endothelial type	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304490
1321820	Lipg	lipase G, endothelial type	gene	MP:0000184	abnormal circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17681148
1321820	Lipg	lipase G, endothelial type	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569160
1321820	Lipg	lipase G, endothelial type	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304490
1321820	Lipg	lipase G, endothelial type	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569160
1321820	Lipg	lipase G, endothelial type	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12601178
1321820	Lipg	lipase G, endothelial type	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304490
1321820	Lipg	lipase G, endothelial type	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569160
1321820	Lipg	lipase G, endothelial type	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12601178
1321820	Lipg	lipase G, endothelial type	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304490
1321820	Lipg	lipase G, endothelial type	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485805
1321820	Lipg	lipase G, endothelial type	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304490
1321820	Lipg	lipase G, endothelial type	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569160
1321820	Lipg	lipase G, endothelial type	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12601178
1321820	Lipg	lipase G, endothelial type	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304490
1321820	Lipg	lipase G, endothelial type	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12601178
1321820	Lipg	lipase G, endothelial type	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304490
1321820	Lipg	lipase G, endothelial type	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15304490
1321822	Zswim5	zinc finger SWIM-type containing 5	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160114	MGI			
1321824	Dact2	dishevelled-binding antagonist of beta-catenin 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20190502	MGI			
1321824	Dact2	dishevelled-binding antagonist of beta-catenin 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1321824	Dact2	dishevelled-binding antagonist of beta-catenin 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20190502	MGI			
1321824	Dact2	dishevelled-binding antagonist of beta-catenin 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1321824	Dact2	dishevelled-binding antagonist of beta-catenin 2	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18716284
1321824	Dact2	dishevelled-binding antagonist of beta-catenin 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1321824	Dact2	dishevelled-binding antagonist of beta-catenin 2	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1321824	Dact2	dishevelled-binding antagonist of beta-catenin 2	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1321824	Dact2	dishevelled-binding antagonist of beta-catenin 2	gene	MP:0012193	increased keratinocyte migration		IAGP		N	RGD:5509061	20141204	MGI			PMID:18716284
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20241121	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220811	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20220811	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210520	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20220811	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210128	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20221215	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20241121	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210520	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415368
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0010207	abnormal telomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321828	Stag1	STAG1 cohesin complex component	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22415365
1321832	Chchd4	coiled-coil-helix-coiled-coil-helix domain containing 4	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20190228	MGI			PMID:26004228
1321832	Chchd4	coiled-coil-helix-coiled-coil-helix domain containing 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20190228	MGI			PMID:26004228
1321832	Chchd4	coiled-coil-helix-coiled-coil-helix domain containing 4	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20190228	MGI			PMID:26178476
1321832	Chchd4	coiled-coil-helix-coiled-coil-helix domain containing 4	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20190228	MGI			PMID:26004228
1321832	Chchd4	coiled-coil-helix-coiled-coil-helix domain containing 4	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20190228	MGI			PMID:26004228
1321834	Cars1	cysteinyl-tRNA synthetase 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1321834	Cars1	cysteinyl-tRNA synthetase 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20260402	MGI			
1321834	Cars1	cysteinyl-tRNA synthetase 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1321834	Cars1	cysteinyl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11439183
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787506
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787506
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11439183
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370307
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787506
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11439183
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370307
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12370307
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0006261	annular pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787506
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554754
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12750314
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11439183
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20260402	MGI			
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11439183
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1321837	Nfatc4	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:12750314
1321840	Agap3	ArfGAP with GTPase domain, ankyrin repeat and PH domain 3	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:33811862
1321840	Agap3	ArfGAP with GTPase domain, ankyrin repeat and PH domain 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210722	MGI			PMID:33811862
1321840	Agap3	ArfGAP with GTPase domain, ankyrin repeat and PH domain 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210722	MGI			PMID:33811862
1321840	Agap3	ArfGAP with GTPase domain, ankyrin repeat and PH domain 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20210722	MGI			PMID:33811862
1321840	Agap3	ArfGAP with GTPase domain, ankyrin repeat and PH domain 3	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20210722	MGI			PMID:33811862
1321840	Agap3	ArfGAP with GTPase domain, ankyrin repeat and PH domain 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210722	MGI			PMID:33811862
1321840	Agap3	ArfGAP with GTPase domain, ankyrin repeat and PH domain 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:33811862
1321843	D430041D05Rik	RIKEN cDNA D430041D05 gene	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20141003	MGI			
1321843	D430041D05Rik	RIKEN cDNA D430041D05 gene	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20141003	MGI			
1321843	D430041D05Rik	RIKEN cDNA D430041D05 gene	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20160728	MGI			PMID:11604496
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20160728	MGI			PMID:11604496
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604496
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604496
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0011184	absent embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:11604496
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0013207	absent endoderm		IAGP		N	RGD:5509061	20160728	MGI			PMID:11604496
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20230727	MGI			PMID:35918532
1321845	Cxxc1	CXXC finger protein 1	gene	MP:0014618	increased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:35918532
1321849	Ifi30	interferon gamma inducible protein 30	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701933
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509662
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509662
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20241121	MGI			
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20241121	MGI			
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509662
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509662
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509662
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20201022	MGI			
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20260402	MGI			
1321851	Asb1	ankyrin repeat and SOCS box-containing 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20220519	MGI			
1321855	Nlk	nemo like kinase	gene	MP:0000168	abnormal bone marrow development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23719801
1321855	Nlk	nemo like kinase	gene	MP:0001454	abnormal cued conditioning behavior		IEA		N	RGD:5509061	20260402	MGI			
1321855	Nlk	nemo like kinase	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1321855	Nlk	nemo like kinase	gene	MP:0001602	impaired myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23719801
1321855	Nlk	nemo like kinase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1321855	Nlk	nemo like kinase	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1321855	Nlk	nemo like kinase	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1321855	Nlk	nemo like kinase	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23719801
1321855	Nlk	nemo like kinase	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23719801
1321855	Nlk	nemo like kinase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11745377
1321855	Nlk	nemo like kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321857	Endog	endonuclease G	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20170105	MGI			
1321857	Endog	endonuclease G	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20170105	MGI			
1321857	Endog	endonuclease G	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20170105	MGI			
1321857	Endog	endonuclease G	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20230601	MGI			
1321857	Endog	endonuclease G	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601850
1321857	Endog	endonuclease G	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16239930
1321857	Endog	endonuclease G	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14663139
1321857	Endog	endonuclease G	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:14663139
1321857	Endog	endonuclease G	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:14663139
1321857	Endog	endonuclease G	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14663139
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20160414	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:19156225
1321862	Itprid2	ITPR interacting domain containing 2	gene	MP:0031414	decreased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:19156225
1321864	Dsc1	desmocollin 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001247	dermal cyst		IAGP		N	RGD:5509061	20160317	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14673151
1321864	Dsc1	desmocollin 1	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0004241	acantholysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0010700	hair follicle comedo		IAGP		N	RGD:5509061	20160317	MGI			PMID:11714727
1321864	Dsc1	desmocollin 1	gene	MP:0030533	abnormal snout skin morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:11714727
1321874	Tmem9b	TMEM9 domain family, member B	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1321874	Tmem9b	TMEM9 domain family, member B	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1321874	Tmem9b	TMEM9 domain family, member B	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1321874	Tmem9b	TMEM9 domain family, member B	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1321874	Tmem9b	TMEM9 domain family, member B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16424905
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:16424905
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:16424905
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321875	Zfand5	zinc finger, AN1-type domain 5	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:17143286
1321876	Rftn1	raftlin lipid raft linker 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414744
1321876	Rftn1	raftlin lipid raft linker 1	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414744
1321876	Rftn1	raftlin lipid raft linker 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414744
1321876	Rftn1	raftlin lipid raft linker 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414744
1321876	Rftn1	raftlin lipid raft linker 1	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414744
1321876	Rftn1	raftlin lipid raft linker 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414744
1321876	Rftn1	raftlin lipid raft linker 1	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414744
1321881	Hoxb3	homeobox B3	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14960494
1321881	Hoxb3	homeobox B3	gene	MP:0001051	abnormal somatic motor system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12954718
1321881	Hoxb3	homeobox B3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748289
1321881	Hoxb3	homeobox B3	gene	MP:0002256	abnormal laryngeal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1321881	Hoxb3	homeobox B3	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1321881	Hoxb3	homeobox B3	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1321881	Hoxb3	homeobox B3	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0003955	abnormal ultimobranchial body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1321881	Hoxb3	homeobox B3	gene	MP:0004445	small exoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0004568	fusion of glossopharyngeal and vagus nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1321881	Hoxb3	homeobox B3	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0004914	absent ultimobranchial body		IAGP		N	RGD:5509061	20150122	MGI			PMID:9520319
1321881	Hoxb3	homeobox B3	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0009899	hyoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1321881	Hoxb3	homeobox B3	gene	MP:0009913	abnormal hyoid bone greater horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0011576	absent cervical atlas		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1321881	Hoxb3	homeobox B3	gene	MP:0013162	abnormal thyroid gland isthmus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1321881	Hoxb3	homeobox B3	gene	MP:0013163	absent thyroid gland isthmus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1321881	Hoxb3	homeobox B3	gene	MP:0013290	persistent ultimobranchial bodies		IAGP		N	RGD:5509061	20150122	MGI			PMID:9520319
1321881	Hoxb3	homeobox B3	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20150305	MGI			PMID:9520319
1321881	Hoxb3	homeobox B3	gene	MP:0030869	thyroid cartilage hypoplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:9441667
1321881	Hoxb3	homeobox B3	gene	MP:0030871	abnormal inferior horn of thyroid cartilage morphology		IAGP		N	RGD:5509061	20181101	MGI			PMID:7913519
1321881	Hoxb3	homeobox B3	gene	MP:0030872	small cricoid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:9441667
1321887	Ska1	spindle and kinetochore associated complex subunit 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1321887	Ska1	spindle and kinetochore associated complex subunit 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1321887	Ska1	spindle and kinetochore associated complex subunit 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20250508	MGI			
1321887	Ska1	spindle and kinetochore associated complex subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1321887	Ska1	spindle and kinetochore associated complex subunit 1	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20250508	MGI			
1321892	Lao1	L-amino acid oxidase 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180607	MGI			PMID:19276171
1321892	Lao1	L-amino acid oxidase 1	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20180607	MGI			PMID:19276171
1321892	Lao1	L-amino acid oxidase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180607	MGI			PMID:19276171
1321892	Lao1	L-amino acid oxidase 1	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20180607	MGI			PMID:19276171
1321892	Lao1	L-amino acid oxidase 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180607	MGI			PMID:19276171
1321892	Lao1	L-amino acid oxidase 1	gene	MP:0013148	mastitis		IAGP		N	RGD:5509061	20180607	MGI			PMID:19276171
1321893	Hvcn1	hydrogen voltage-gated channel 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285483
1321893	Hvcn1	hydrogen voltage-gated channel 1	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285483
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221124	MGI			PMID:31765609
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20221124	MGI			PMID:31765609
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20221124	MGI			PMID:31765609
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17036046
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000524	decreased renal tubule number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17036046
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682239
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682239
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0000533	kidney hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17036046
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682239
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053786
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17036046
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17036046
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0003624	anuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17036046
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0004755	abnormal loop of Henle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17036046
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221124	MGI			PMID:31765609
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17036046
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682239
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210603	MGI			PMID:27542690
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221124	MGI			PMID:31765609
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011289	abnormal nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17036046
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011363	renal glomerulus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011371	decreased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23360989
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011387	absent metanephric mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011457	abnormal metanephric ureteric bud development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20299358
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011856	abnormal glomerular filtration barrier function		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0011869	detached podocyte		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20221124	MGI			PMID:31765609
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:31765609
1321898	Six2	sine oculis-related homeobox 2	gene	MP:0021217	abnormal palatal shelf bone ossification		IAGP		N	RGD:5509061	20230302	MGI			PMID:31765609
1321900	Rras2	RAS oncogene related 2	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20230119	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20230119	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0001264	increased body size		IEA		N	RGD:5509061	20141003	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0001326	retina degeneration		IEA		N	RGD:5509061	20141003	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20141003	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IEA		N	RGD:5509061	20141003	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IEA		N	RGD:5509061	20141003	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20230119	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0008515	thin retina outer nuclear layer		IEA		N	RGD:5509061	20141003	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19561613
1321900	Rras2	RAS oncogene related 2	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230119	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20141003	MGI			
1321900	Rras2	RAS oncogene related 2	gene	MP:0014348	decreased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:19561613
1321903	Kremen2	kringle containing transmembrane protein 2	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505822
1321903	Kremen2	kringle containing transmembrane protein 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505822
1321903	Kremen2	kringle containing transmembrane protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505822
1321903	Kremen2	kringle containing transmembrane protein 2	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505822
1321903	Kremen2	kringle containing transmembrane protein 2	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505822
1321903	Kremen2	kringle containing transmembrane protein 2	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18505822
1321903	Kremen2	kringle containing transmembrane protein 2	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:18505822
1321903	Kremen2	kringle containing transmembrane protein 2	gene	MP:0020080	increased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:18505822
1321908	Chst4	carbohydrate sulfotransferase 4	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520459
1321908	Chst4	carbohydrate sulfotransferase 4	gene	MP:0002345	abnormal lymph node primary follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520459
1321908	Chst4	carbohydrate sulfotransferase 4	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520459
1321908	Chst4	carbohydrate sulfotransferase 4	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14593101
1321908	Chst4	carbohydrate sulfotransferase 4	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254996
1321908	Chst4	carbohydrate sulfotransferase 4	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520459
1321908	Chst4	carbohydrate sulfotransferase 4	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:14593101
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160421	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20160421	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20260402	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160421	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20160421	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20170105	MGI			
1321910	Fam53b	family with sequence similarity 53, member B	gene	MP:0011951	increased cardiac stroke volume		IEA		N	RGD:5509061	20211021	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20221215	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200917	MGI			PMID:32814042
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220811	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200917	MGI			PMID:32814042
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20221215	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20221215	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1321912	Pcif1	phosphorylated CTD interacting factor 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220811	MGI			
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361867
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361867
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325042
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485447
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0002913	abnormal PNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325042
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325042
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0003903	increased cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17277770
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325042
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17277770
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361867
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0004836	abnormal synaptic acetylcholine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:17325042
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199140
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485447
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361867
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17277770
1321916	Gabpa	GA repeat binding protein, alpha	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:17277770
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20210520	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20170105	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20170105	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170105	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20180118	MGI			PMID:24889031
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20170105	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20170105	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20180118	MGI			PMID:24889031
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20181227	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20180118	MGI			PMID:24889031
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20180118	MGI			PMID:24889031
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0010422	heart right ventricle hypoplasia		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20180118	MGI			PMID:24889031
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201022	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0012117	decreased trophectoderm cell proliferation		IAGP		N	RGD:5509061	20180118	MGI			PMID:24889031
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0012128	abnormal blastocyst formation		IAGP		N	RGD:5509061	20180118	MGI			PMID:24889031
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180118	MGI			PMID:24889031
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321921	Mmachc	methylmalonic aciduria cblC type, with homocystinuria	gene	MP:0030630	increased circulating methylmalonic acid level		IAGP		N	RGD:5509061	20210128	MGI			PMID:32941884
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:27162334
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0003381	vitreal fibroplasia		IEA		N	RGD:5509061	20111116	MGI			
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12651948
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12651948
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679561
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12651948
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679561
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12651948
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679561
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679561
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679561
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679561
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20171207	MGI			PMID:28859131
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20171207	MGI			PMID:28859131
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20171207	MGI			PMID:28859131
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20171207	MGI			PMID:28859131
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0012671	retina spots		IEA		N	RGD:5509061	20141003	MGI			
1321923	Rpgrip1	retinitis pigmentosa GTPase regulator interacting protein 1	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:28859131
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343150
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15593327
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483628
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15593327
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224648
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343150
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483628
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15593327
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224648
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:22162625
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343150
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001309	hydropic eye lens fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483628
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20220519	MGI			
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20220519	MGI			
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343150
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15593327
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19224648
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483628
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343150
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483628
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0005102	abnormal iris pigmentation		IEA		N	RGD:5509061	20220519	MGI			
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15483628
1321925	Hsf4	heat shock transcription factor 4	gene	MP:0031428	lens dislocation		IAGP		N	RGD:5509061	20220714	MGI			PMID:15343150
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20170105	MGI			
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20230601	MGI			
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240222	MGI			PMID:33932340
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20170105	MGI			
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180222	MGI			PMID:28106097
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20240222	MGI			PMID:27936058
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20170105	MGI			
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20240222	MGI			PMID:27936058
1321927	Lancl2	LanC (bacterial lantibiotic synthetase component C)-like 2	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20240222	MGI			PMID:27936058
1321928	Pomk	protein-O-mannose kinase	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1321928	Pomk	protein-O-mannose kinase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1321928	Pomk	protein-O-mannose kinase	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1321928	Pomk	protein-O-mannose kinase	gene	MP:0002635	reduced sensorimotor gating		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230601	MGI			
1321928	Pomk	protein-O-mannose kinase	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0010008	abnormal Purkinje cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321928	Pomk	protein-O-mannose kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1321928	Pomk	protein-O-mannose kinase	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210826	MGI			
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0014246	decreased cellular ATP level		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0030718	increased circulating lysine level		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0030721	increased lysine level		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321930	Aass	aminoadipate-semialdehyde synthase	gene	MP:0031022	hepatic megalocytosis		IAGP		N	RGD:5509061	20260813	MGI			PMID:30573525
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160114	MGI			
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20160114	MGI			
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0005358	abnormal incisor morphology		IEA		N	RGD:5509061	20201022	MGI			
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20210527	MGI			PMID:33691104
1321932	Tchp	trichoplein, keratin filament binding	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:33691104
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001117	absent gametes		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0008878	abnormal DNA methylation during gametogenesis		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0010772	abnormal pollex morphology		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0013707	abnormal hematopoietic precursor cell morphology		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0014040	increased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20211209	MGI			PMID:34373449
1321934	Fanci	Fanconi anemia, complementation group I	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20211216	MGI			PMID:31219578
1321935	Klhl25	kelch-like 25	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20181122	MGI			
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15383458
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834123
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0009623	enlarged inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371358
1321938	Gpr132	G protein-coupled receptor 132	gene	MP:0011081	decreased macrophage apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15834123
1321939	Obox6	oocyte specific homeobox 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676645
1321940	Cracdl	capping protein inhibiting regulator of actin like	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1321940	Cracdl	capping protein inhibiting regulator of actin like	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20201022	MGI			
1321940	Cracdl	capping protein inhibiting regulator of actin like	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1321940	Cracdl	capping protein inhibiting regulator of actin like	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20201022	MGI			
1321940	Cracdl	capping protein inhibiting regulator of actin like	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20201022	MGI			
1321942	Col15a1	collagen, type XV, alpha 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158616
1321942	Col15a1	collagen, type XV, alpha 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158616
1321942	Col15a1	collagen, type XV, alpha 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158616
1321942	Col15a1	collagen, type XV, alpha 1	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158616
1321942	Col15a1	collagen, type XV, alpha 1	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158616
1321942	Col15a1	collagen, type XV, alpha 1	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158616
1321942	Col15a1	collagen, type XV, alpha 1	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:11158616
1321944	Dolk	dolichol kinase	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191205	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0003107	abnormal response to novelty		IEA		N	RGD:5509061	20170413	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0003360	abnormal depression-related behavior		IEA		N	RGD:5509061	20170413	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0005407	hyperalgesia		IEA		N	RGD:5509061	20170413	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170413	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1321944	Dolk	dolichol kinase	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241128	MGI			
1321945	Cttnbp2nl	CTTNBP2 N-terminal like	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1321945	Cttnbp2nl	CTTNBP2 N-terminal like	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1321945	Cttnbp2nl	CTTNBP2 N-terminal like	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230601	MGI			
1321945	Cttnbp2nl	CTTNBP2 N-terminal like	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20220811	MGI			
1321945	Cttnbp2nl	CTTNBP2 N-terminal like	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1321947	Recql5	RecQ protein-like 5	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831450
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237163
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237163
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237163
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0014373	increased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0014375	increased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0014384	increased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:23172145
1321949	Eif4ebp2	eukaryotic translation initiation factor 4E binding protein 2	gene	MP:0031334	increased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:23172145
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20181227	MGI			
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20181227	MGI			
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20181227	MGI			
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20231207	MGI			
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20240404	MGI			PMID:38517960
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0009454	impaired contextual conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0009516	enlarged salivary gland		IEA		N	RGD:5509061	20181227	MGI			
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0010283	decreased classified tumor incidence		IAGP		N	RGD:5509061	20240404	MGI			PMID:38517960
1321951	Pgbd5	piggyBac transposable element derived 5	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20240404	MGI			PMID:38517960
1321953	Actr2	actin related protein 2	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20180322	MGI			PMID:28827327
1321954	Tril	TLR4 interactor with leucine-rich repeats	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20210401	MGI			PMID:25015823
1321954	Tril	TLR4 interactor with leucine-rich repeats	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20210401	MGI			PMID:25015823
1321954	Tril	TLR4 interactor with leucine-rich repeats	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20210401	MGI			PMID:25015823
1321954	Tril	TLR4 interactor with leucine-rich repeats	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20210401	MGI			PMID:25015823
1321954	Tril	TLR4 interactor with leucine-rich repeats	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20210401	MGI			PMID:25015823
1321955	Tmem129	transmembrane protein 129	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1321955	Tmem129	transmembrane protein 129	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1321955	Tmem129	transmembrane protein 129	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1321955	Tmem129	transmembrane protein 129	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1321955	Tmem129	transmembrane protein 129	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1321955	Tmem129	transmembrane protein 129	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1321955	Tmem129	transmembrane protein 129	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1321962	Riok3	RIO kinase 3	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1321962	Riok3	RIO kinase 3	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1321962	Riok3	RIO kinase 3	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230601	MGI			
1321962	Riok3	RIO kinase 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1321962	Riok3	RIO kinase 3	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20240523	MGI			
1321962	Riok3	RIO kinase 3	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1321967	Ptges2	prostaglandin E synthase 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1321967	Ptges2	prostaglandin E synthase 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1321967	Ptges2	prostaglandin E synthase 2	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1321968	Lpcat2b	lysophosphatidylcholine acyltransferase 2B	gene	MP:0005544	cornea deposits		IEA		N	RGD:5509061	20181227	MGI			
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0001011	abnormal superior cervical ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160825	MGI			PMID:14634087
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003708	binucleate		IAGP		N	RGD:5509061	20250814	MGI			PMID:24141881
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0008312	abnormal sympathetic postganglionic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0009891	abnormal palate bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010405	ostium secundum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010587	conotruncal ridge hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010589	common truncal valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0010652	absent aorticopulmonary septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19412548
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24141881
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0030168	thin upper lip		IAGP		N	RGD:5509061	20171005	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0030243	abnormal chin morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0030244	short chin		IAGP		N	RGD:5509061	20171019	MGI			PMID:17652350
1321970	Pds5b	PDS5 cohesin associated factor B	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:24141881
1321973	Tagln2	transgelin 2	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1321973	Tagln2	transgelin 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1321973	Tagln2	transgelin 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1321973	Tagln2	transgelin 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20180315	MGI			PMID:25869671
1321973	Tagln2	transgelin 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1321973	Tagln2	transgelin 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20180315	MGI			PMID:25869671
1321973	Tagln2	transgelin 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1321973	Tagln2	transgelin 2	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1321973	Tagln2	transgelin 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1321973	Tagln2	transgelin 2	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20180315	MGI			PMID:25869671
1321973	Tagln2	transgelin 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20201022	MGI			
1321973	Tagln2	transgelin 2	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1321975	Zbtb21	zinc finger and BTB domain containing 21	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1321975	Zbtb21	zinc finger and BTB domain containing 21	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1321975	Zbtb21	zinc finger and BTB domain containing 21	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1321975	Zbtb21	zinc finger and BTB domain containing 21	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1321975	Zbtb21	zinc finger and BTB domain containing 21	gene	MP:0031751	abnormal inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20260813	MGI			PMID:38959316
1321980	Dusp10	dual specificity phosphatase 10	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15306813
1321980	Dusp10	dual specificity phosphatase 10	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15306813
1321980	Dusp10	dual specificity phosphatase 10	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15306813
1321980	Dusp10	dual specificity phosphatase 10	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15306813
1321980	Dusp10	dual specificity phosphatase 10	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15306813
1321980	Dusp10	dual specificity phosphatase 10	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15306813
1321980	Dusp10	dual specificity phosphatase 10	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15306813
1321980	Dusp10	dual specificity phosphatase 10	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15306813
1321980	Dusp10	dual specificity phosphatase 10	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15306813
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0000525	renal tubular acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723628
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723628
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0002876	abnormal thyroid gland physiology		IAGP		N	RGD:5509061	20220630	MGI			PMID:30333321
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723628
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0003030	acidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723628
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20220630	MGI			PMID:30333321
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723628
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:30333321
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20220630	MGI			PMID:30333321
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0005355	enlarged thyroid gland		IAGP		N	RGD:5509061	20220630	MGI			PMID:30333321
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0005468	abnormal thyroid hormone level		IAGP		N	RGD:5509061	20220630	MGI			PMID:30333321
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20220630	MGI			PMID:30333321
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20220630	MGI			PMID:30333321
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723628
1321984	Slc26a7	solute carrier family 26, member 7	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723628
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20220825	MGI			PMID:35044787
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230119	MGI			
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230119	MGI			
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230119	MGI			
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20220825	MGI			PMID:35044787
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20220825	MGI			PMID:35044787
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20220825	MGI			PMID:35044787
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20220825	MGI			PMID:35044787
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20220825	MGI			PMID:35044787
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20220825	MGI			PMID:35044787
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20220825	MGI			PMID:35044787
1321986	Bag5	BCL2-associated athanogene 5	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:35044787
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20170105	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539757
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20240627	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539757
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1321988	Gpr22	G protein-coupled receptor 22	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1321990	Ipo7	importin 7	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210520	MGI			
1321990	Ipo7	importin 7	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1321990	Ipo7	importin 7	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1321990	Ipo7	importin 7	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1321990	Ipo7	importin 7	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1321990	Ipo7	importin 7	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1321990	Ipo7	importin 7	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1321990	Ipo7	importin 7	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220519	MGI			
1321990	Ipo7	importin 7	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1321990	Ipo7	importin 7	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20221215	MGI			
1321990	Ipo7	importin 7	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1321990	Ipo7	importin 7	gene	MP:0002282	abnormal trachea morphology		IEA		N	RGD:5509061	20210520	MGI			
1321990	Ipo7	importin 7	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1321990	Ipo7	importin 7	gene	MP:0004957	abnormal blastocyst morphology		IEA		N	RGD:5509061	20240919	MGI			
1321990	Ipo7	importin 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1321990	Ipo7	importin 7	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1321990	Ipo7	importin 7	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240919	MGI			
1321991	Asb18	ankyrin repeat and SOCS box-containing 18	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1321991	Asb18	ankyrin repeat and SOCS box-containing 18	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20201105	MGI			PMID:32839317
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20201105	MGI			PMID:32839317
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20221215	MGI			
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20201105	MGI			PMID:32839317
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20201105	MGI			PMID:32839317
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20221215	MGI			
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201105	MGI			PMID:32839317
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20201105	MGI			PMID:32839317
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0020581	abnormal neuron polarity		IAGP		N	RGD:5509061	20201105	MGI			PMID:32839317
1321993	Camsap1	calmodulin regulated spectrin-associated protein 1	gene	MP:0020850	abnormal microtubule cytoskeleton morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:32839317
1321996	Phf11d	PHD finger protein 11D	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20151022	MGI			PMID:25091723
1322001	Coq5	coenzyme Q5 methyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1322003	Grsf1	G-rich RNA sequence binding factor 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1322005	Ushbp1	USH1 protein network component harmonin binding protein 1	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20160114	MGI			
1322011	Slc39a3	solute carrier family 39 (zinc transporter), member 3	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1322011	Slc39a3	solute carrier family 39 (zinc transporter), member 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1322011	Slc39a3	solute carrier family 39 (zinc transporter), member 3	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964816
1322011	Slc39a3	solute carrier family 39 (zinc transporter), member 3	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964816
1322011	Slc39a3	solute carrier family 39 (zinc transporter), member 3	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1322011	Slc39a3	solute carrier family 39 (zinc transporter), member 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1322011	Slc39a3	solute carrier family 39 (zinc transporter), member 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964816
1322011	Slc39a3	solute carrier family 39 (zinc transporter), member 3	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1322011	Slc39a3	solute carrier family 39 (zinc transporter), member 3	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964816
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17070806
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0004038	lymphangiectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17070806
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1322013	Lyve1	lymphatic vessel endothelial hyaluronan receptor 1	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20026661
1322015	Krt7	keratin 7	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1322015	Krt7	keratin 7	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1322015	Krt7	keratin 7	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23741325
1322015	Krt7	keratin 7	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20210128	MGI			
1322015	Krt7	keratin 7	gene	MP:0010386	abnormal urinary bladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23741325
1322018	Pitpnm2	phosphatidylinositol transfer protein, membrane-associated 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11744244
1322019	Engase	endo-beta-N-acetylglucosaminidase	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20210923	MGI			PMID:34215698
1322027	Trabd	TraB domain containing	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20210520	MGI			
1322029	Il22ra2	interleukin 22 receptor, alpha 2	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23075849
1322029	Il22ra2	interleukin 22 receptor, alpha 2	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23075849
1322029	Il22ra2	interleukin 22 receptor, alpha 2	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23075849
1322029	Il22ra2	interleukin 22 receptor, alpha 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23075849
1322029	Il22ra2	interleukin 22 receptor, alpha 2	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:23075849
1322031	Yeats2	YEATS domain containing 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1322031	Yeats2	YEATS domain containing 2	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210128	MGI			
1322031	Yeats2	YEATS domain containing 2	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20210128	MGI			
1322031	Yeats2	YEATS domain containing 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1322031	Yeats2	YEATS domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322031	Yeats2	YEATS domain containing 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322032	Mthfd2l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20160811	MGI			
1322032	Mthfd2l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20160811	MGI			
1322032	Mthfd2l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1322036	Terf2	telomeric repeat binding factor 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015429
1322036	Terf2	telomeric repeat binding factor 2	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015429
1322036	Terf2	telomeric repeat binding factor 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15968270
1322038	Parvg	parvin, gamma	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16479001
1322040	Fpr1	formyl peptide receptor 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989980
1322040	Fpr1	formyl peptide receptor 1	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989980
1322040	Fpr1	formyl peptide receptor 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989980
1322040	Fpr1	formyl peptide receptor 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9989980
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084104
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084104
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084104
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084104
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084104
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809042
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0003896	prolonged PR interval		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084104
1322042	Barx1	BarH-like homeobox 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809042
1322042	Barx1	BarH-like homeobox 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20260402	MGI			
1322042	Barx1	BarH-like homeobox 1	gene	MP:0011971	increased circulating lactate dehydrogenase level		IEA		N	RGD:5509061	20260402	MGI			
1322044	Diablo	diablo, IAP-binding mitochondrial protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509788
1322044	Diablo	diablo, IAP-binding mitochondrial protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509788
1322044	Diablo	diablo, IAP-binding mitochondrial protein	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509788
1322044	Diablo	diablo, IAP-binding mitochondrial protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971981
1322044	Diablo	diablo, IAP-binding mitochondrial protein	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509788
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20241121	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660741
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230119	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660741
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241121	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660741
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660741
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828507
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828507
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828507
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828507
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828507
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828507
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828507
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190307	MGI			PMID:30106088
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660741
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20660741
1322046	Zfat	zinc finger and AT hook domain containing	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20240523	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20141003	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20141003	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20141003	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20141003	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20141003	MGI			
1322048	Miga2	mitoguardin 2	gene	MP:0012479	increased amygdala size		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0014414	increased depression-related behavior		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0014527	increased amino acid level		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0031487	increased circulating hypoxanthine level		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322048	Miga2	mitoguardin 2	gene	MP:0031490	increased circulating xanthine level		IAGP		N	RGD:5509061	20240926	MGI			PMID:31675497
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382243
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382243
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382243
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892650
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11201745
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892650
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382243
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382243
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11201745
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892650
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892650
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382243
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892650
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23187126
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:23382243
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892650
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20141003	MGI			PMID:17210695
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892650
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382243
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892650
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0011194	abnormal hair follicle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382243
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892650
1322051	Mad2l1	MAD2 mitotic arrest deficient-like 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:10892650
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964481
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964481
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262402
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262402
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0005413	vascular restenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964481
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20200917	MGI			PMID:11964481
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262402
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262402
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0009818	abnormal thromboxane level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11964481
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9262402
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:16614756
1322053	Ptgir	prostaglandin I receptor (IP)	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:9262402
1322061	Kbtbd3	kelch repeat and BTB (POZ) domain containing 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1322061	Kbtbd3	kelch repeat and BTB (POZ) domain containing 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1322061	Kbtbd3	kelch repeat and BTB (POZ) domain containing 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1322061	Kbtbd3	kelch repeat and BTB (POZ) domain containing 3	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20241121	MGI			
1322065	Pmm1	phosphomannomutase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847318
1322067	Scml4	Scm polycomb group protein like 4	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1322067	Scml4	Scm polycomb group protein like 4	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20201231	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20241010	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20241010	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20231207	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20241010	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20241010	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1322071	Mtpap	mitochondrial poly(A) polymerase	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210826	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20210826	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20210826	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210826	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210826	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210826	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220519	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230601	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210826	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210826	MGI			
1322073	Dpp8	dipeptidylpeptidase 8	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220519	MGI			
1322075	Nudt12	nudix hydrolase 12	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20200109	MGI			PMID:31875550
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20230601	MGI			
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0004266	pale placenta		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0011531	abnormal syncytiotrophoblast morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20230601	MGI			
1322083	Tlk2	tousled-like kinase 2 (Arabidopsis)	gene	MP:0030989	decreased spongiotrophoblast cell number		IAGP		N	RGD:5509061	20191219	MGI			PMID:28708136
1322087	Sema6d	sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:28172500
1322087	Sema6d	sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20190912	MGI			PMID:28172500
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210520	MGI			
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0002704	tubular nephritis		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0005556	abnormal renal filtration rate		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0011483	renal glomerular synechia		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322089	Cmas	cytidine monophospho-N-acetylneuraminic acid synthetase	gene	MP:0011868	podocyte microvillus transformation		IAGP		N	RGD:5509061	20200416	MGI			PMID:31040189
1322091	Eps8l2	EPS8-like 2	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20181227	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0002102	abnormal ear morphology		IEA		N	RGD:5509061	20181227	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200402	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0004417	decreased cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0004524	short cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0004534	decreased inner hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0006335	abnormal hearing electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0006388	abnormal auditory summating potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0009456	impaired cued conditioning behavior		IEA		N	RGD:5509061	20230601	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20181227	MGI			
1322091	Eps8l2	EPS8-like 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918390
1322091	Eps8l2	EPS8-like 2	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20241121	MGI			
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767368
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0004182	abnormal spermiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767368
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322094	Pip5k1b	phosphatidylinositol-4-phosphate 5-kinase, type 1 beta	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22321832
1322099	Igdcc4	immunoglobulin superfamily, DCC subclass, member 4	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20220224	MGI			PMID:34871331
1322099	Igdcc4	immunoglobulin superfamily, DCC subclass, member 4	gene	MP:0031045	decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20220224	MGI			PMID:34871331
1322102	Snx14	sorting nexin 14	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1322102	Snx14	sorting nexin 14	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20201022	MGI			
1322102	Snx14	sorting nexin 14	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1322102	Snx14	sorting nexin 14	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1322102	Snx14	sorting nexin 14	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322107	Dyrk3	dual-specificity tyrosine phosphorylation regulated kinase 3	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854306
1322107	Dyrk3	dual-specificity tyrosine phosphorylation regulated kinase 3	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20210805	MGI			PMID:18854306
1322108	Snrnp27	small nuclear ribonucleoprotein 27 (U4/U6.U5)	gene	MP:0000467	abnormal esophagus morphology		IEA		N	RGD:5509061	20160811	MGI			
1322108	Snrnp27	small nuclear ribonucleoprotein 27 (U4/U6.U5)	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1322108	Snrnp27	small nuclear ribonucleoprotein 27 (U4/U6.U5)	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1322108	Snrnp27	small nuclear ribonucleoprotein 27 (U4/U6.U5)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322108	Snrnp27	small nuclear ribonucleoprotein 27 (U4/U6.U5)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322108	Snrnp27	small nuclear ribonucleoprotein 27 (U4/U6.U5)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0002580	duodenal lesions		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0009311	increased duodenum adenocarcinoma incidence		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17517967
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0012408	increased duodenum glandular epithelium tumor incidence		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0013482	abnormal duodenum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20170629	MGI			PMID:27229122
1322109	B3gnt6	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160304	MGI			PMID:17517967
1322112	Xpo7	exportin 7	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0013659	abnormal erythroid lineage cell morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322112	Xpo7	exportin 7	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20221215	MGI			PMID:35973480
1322114	Zim1	zinc finger, imprinted 1	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20241121	MGI			
1322114	Zim1	zinc finger, imprinted 1	gene	MP:0010896	decreased lung compliance		IEA		N	RGD:5509061	20241121	MGI			
1322114	Zim1	zinc finger, imprinted 1	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20241121	MGI			
1322114	Zim1	zinc finger, imprinted 1	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20241121	MGI			
1322114	Zim1	zinc finger, imprinted 1	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20241121	MGI			
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15018652
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14654002
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143267
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14654002
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20211104	MGI			PMID:26692333
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143267
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441929
1322116	Dppa3	developmental pluripotency-associated 3	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20251023	MGI			PMID:36919611
1322125	Slc49a4	solute carrier family 49 member 4	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210520	MGI			
1322125	Slc49a4	solute carrier family 49 member 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1322125	Slc49a4	solute carrier family 49 member 4	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20210520	MGI			
1322127	Miga1	mitoguardin 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1322127	Miga1	mitoguardin 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1322127	Miga1	mitoguardin 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1322127	Miga1	mitoguardin 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1322127	Miga1	mitoguardin 1	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20160811	MGI			
1322127	Miga1	mitoguardin 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1322130	Idua	iduronidase, alpha-L	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576554
1322130	Idua	iduronidase, alpha-L	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0000346	broad head		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111796
1322130	Idua	iduronidase, alpha-L	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20170907	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20241121	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20170907	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0000731	increased collagen deposition in the muscles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20241121	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20240523	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20170907	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20240523	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0001462	abnormal avoidance learning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473336
1322130	Idua	iduronidase, alpha-L	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18511319
1322130	Idua	iduronidase, alpha-L	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473336
1322130	Idua	iduronidase, alpha-L	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111796
1322130	Idua	iduronidase, alpha-L	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0003211	abnormal aorta elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576554
1322130	Idua	iduronidase, alpha-L	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0003898	abnormal QRS complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0003929	decreased heart rate variability		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576554
1322130	Idua	iduronidase, alpha-L	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111796
1322130	Idua	iduronidase, alpha-L	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111796
1322130	Idua	iduronidase, alpha-L	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20240523	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0004864	spiral ligament degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20260402	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20240523	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111796
1322130	Idua	iduronidase, alpha-L	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111796
1322130	Idua	iduronidase, alpha-L	gene	MP:0006045	mitral valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20250508	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0009840	abnormal foam cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111796
1322130	Idua	iduronidase, alpha-L	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0010429	abnormal heart left ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20231109	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0010618	enlarged mitral valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0010627	enlarged tricuspid valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1322130	Idua	iduronidase, alpha-L	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1322130	Idua	iduronidase, alpha-L	gene	MP:0010941	abnormal foramen magnum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15111796
1322130	Idua	iduronidase, alpha-L	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20171012	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0011021	abnormal circadian regulation of heart rate		IAGP		N	RGD:5509061	20171012	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920451
1322130	Idua	iduronidase, alpha-L	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022143
1322130	Idua	iduronidase, alpha-L	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20250508	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0011896	increased circulating unsaturated transferrin level		IEA		N	RGD:5509061	20250508	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20240523	MGI			
1322130	Idua	iduronidase, alpha-L	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101178
1322130	Idua	iduronidase, alpha-L	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1322130	Idua	iduronidase, alpha-L	gene	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0020242	increased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0021161	increased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0021163	increased heart left ventricle septal wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:15979918
1322130	Idua	iduronidase, alpha-L	gene	MP:0030037	prominent nasal bridge		IAGP		N	RGD:5509061	20170914	MGI			PMID:9660052
1322130	Idua	iduronidase, alpha-L	gene	MP:0030069	broad face		IAGP		N	RGD:5509061	20170921	MGI			PMID:9097952
1322130	Idua	iduronidase, alpha-L	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:19751987
1322130	Idua	iduronidase, alpha-L	gene	MP:0030796	hip dislocation		IAGP		N	RGD:5509061	20181025	MGI			PMID:9660052
1322132	Naa50	N(alpha)-acetyltransferase 50, NatE catalytic subunit	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1322132	Naa50	N(alpha)-acetyltransferase 50, NatE catalytic subunit	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1322132	Naa50	N(alpha)-acetyltransferase 50, NatE catalytic subunit	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20241121	MGI			
1322132	Naa50	N(alpha)-acetyltransferase 50, NatE catalytic subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322132	Naa50	N(alpha)-acetyltransferase 50, NatE catalytic subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1322132	Naa50	N(alpha)-acetyltransferase 50, NatE catalytic subunit	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1322135	Papolb	poly (A) polymerase beta (testis specific)	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20201022	MGI			
1322135	Papolb	poly (A) polymerase beta (testis specific)	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1322135	Papolb	poly (A) polymerase beta (testis specific)	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471261
1322135	Papolb	poly (A) polymerase beta (testis specific)	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471261
1322135	Papolb	poly (A) polymerase beta (testis specific)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471261
1322135	Papolb	poly (A) polymerase beta (testis specific)	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12471261
1322135	Papolb	poly (A) polymerase beta (testis specific)	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210520	MGI			
1322135	Papolb	poly (A) polymerase beta (testis specific)	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:12471261
1322137	Dynlt2a1	dynein light chain Tctex-type 2A1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778998
1322137	Dynlt2a1	dynein light chain Tctex-type 2A1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778998
1322137	Dynlt2a1	dynein light chain Tctex-type 2A1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778998
1322137	Dynlt2a1	dynein light chain Tctex-type 2A1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778998
1322137	Dynlt2a1	dynein light chain Tctex-type 2A1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778998
1322137	Dynlt2a1	dynein light chain Tctex-type 2A1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778998
1322137	Dynlt2a1	dynein light chain Tctex-type 2A1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778998
1322137	Dynlt2a1	dynein light chain Tctex-type 2A1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778998
1322137	Dynlt2a1	dynein light chain Tctex-type 2A1	gene	MP:0009839	multiflagellated sperm		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778998
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20160310	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675333
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0005099	abnormal ciliary body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20160310	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746917
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0010405	ostium secundum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10675333
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011393	decreased fetal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20250605	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:21041952
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20160310	MGI			PMID:9030684
1322141	Sos1	SOS Ras/Rac guanine nucleotide exchange factor 1	gene	MP:0014990	enhanced erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:21041952
1322144	E130308A19Rik	RIKEN cDNA E130308A19 gene	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1322144	E130308A19Rik	RIKEN cDNA E130308A19 gene	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418887
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20201022	MGI			
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418887
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418887
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418887
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418887
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418887
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418887
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0008462	abnormal medium spiny neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418887
1322152	Slitrk5	SLIT and NTRK-like family, member 5	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418887
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20240523	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20241010	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0014384	increased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0020358	abnormal inhibitory synapse morphology		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322155	Clptm1	cleft lip and palate associated transmembrane protein 1	gene	MP:0031334	increased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20251120	MGI			PMID:38942471
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0030250	frontonasal prominence hypoplasia		IAGP		N	RGD:5509061	20171019	MGI			PMID:18385133
1322157	Ndst3	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20171109	MGI			PMID:18385133
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210826	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220519	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220519	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220519	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20210520	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210520	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210826	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210520	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20210520	MGI			
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0010645	failure of conotruncal ridge closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0010651	aorticopulmonary septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015483
1322159	Ssr1	signal sequence receptor, alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1322161	Btbd1	BTB domain containing 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1322161	Btbd1	BTB domain containing 1	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20200514	MGI			
1322161	Btbd1	BTB domain containing 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
1322161	Btbd1	BTB domain containing 1	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20240523	MGI			
1322165	Ikzf5	IKAROS family zinc finger 5	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1322165	Ikzf5	IKAROS family zinc finger 5	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1322165	Ikzf5	IKAROS family zinc finger 5	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1322165	Ikzf5	IKAROS family zinc finger 5	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1322167	Dok2	docking protein 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1322167	Dok2	docking protein 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1322167	Dok2	docking protein 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1322167	Dok2	docking protein 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1322167	Dok2	docking protein 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1322167	Dok2	docking protein 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1322167	Dok2	docking protein 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1322167	Dok2	docking protein 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1322167	Dok2	docking protein 2	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1322167	Dok2	docking protein 2	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1322167	Dok2	docking protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1322167	Dok2	docking protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1322167	Dok2	docking protein 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1322167	Dok2	docking protein 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1322167	Dok2	docking protein 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1322167	Dok2	docking protein 2	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611295
1322167	Dok2	docking protein 2	gene	MP:0004202	pulmonary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1322167	Dok2	docking protein 2	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1322167	Dok2	docking protein 2	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1322167	Dok2	docking protein 2	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1322167	Dok2	docking protein 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322167	Dok2	docking protein 2	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1322167	Dok2	docking protein 2	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1322167	Dok2	docking protein 2	gene	MP:0010829	increased bronchioalveolar stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1322167	Dok2	docking protein 2	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15611294
1322172	Ino80	INO80 complex subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1322172	Ino80	INO80 complex subunit	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20210826	MGI			
1322172	Ino80	INO80 complex subunit	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20160811	MGI			
1322172	Ino80	INO80 complex subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20151224	MGI			
1322172	Ino80	INO80 complex subunit	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20201231	MGI			
1322172	Ino80	INO80 complex subunit	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0008402	increased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0008409	increased cellular sensitivity to hydroxyurea induced cell death		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0010207	abnormal telomere morphology		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20210826	MGI			
1322172	Ino80	INO80 complex subunit	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20160414	MGI			PMID:26975355
1322172	Ino80	INO80 complex subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322172	Ino80	INO80 complex subunit	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0012159	absent anterior visceral endoderm		IAGP		N	RGD:5509061	20160414	MGI			PMID:26975355
1322172	Ino80	INO80 complex subunit	gene	MP:0012161	absent distal visceral endoderm		IAGP		N	RGD:5509061	20160414	MGI			PMID:26975355
1322172	Ino80	INO80 complex subunit	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20170608	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:23979016
1322172	Ino80	INO80 complex subunit	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:23979016
1322174	Clasp1	CLIP associating protein 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210128	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210520	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20221215	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20210826	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1322174	Clasp1	CLIP associating protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322176	Mtmr3	myotubularin related protein 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1322176	Mtmr3	myotubularin related protein 3	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1322176	Mtmr3	myotubularin related protein 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20111116	MGI			
1322176	Mtmr3	myotubularin related protein 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20111116	MGI			
1322176	Mtmr3	myotubularin related protein 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1322176	Mtmr3	myotubularin related protein 3	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20231207	MGI			
1322176	Mtmr3	myotubularin related protein 3	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20220811	MGI			
1322176	Mtmr3	myotubularin related protein 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1322179	Sorcs3	sortilin-related VPS10 domain containing receptor 3	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:24069373
1322179	Sorcs3	sortilin-related VPS10 domain containing receptor 3	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:24069373
1322179	Sorcs3	sortilin-related VPS10 domain containing receptor 3	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:24069373
1322179	Sorcs3	sortilin-related VPS10 domain containing receptor 3	gene	MP:0012312	impaired avoidance learning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:24069373
1322180	Pde12	phosphodiesterase 12	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1322180	Pde12	phosphodiesterase 12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322180	Pde12	phosphodiesterase 12	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1322183	Epm2aip1	EPM2A interacting protein 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24142699
1322183	Epm2aip1	EPM2A interacting protein 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24142699
1322183	Epm2aip1	EPM2A interacting protein 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24142699
1322183	Epm2aip1	EPM2A interacting protein 1	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24142699
1322183	Epm2aip1	EPM2A interacting protein 1	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24142699
1322183	Epm2aip1	EPM2A interacting protein 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24142699
1322183	Epm2aip1	EPM2A interacting protein 1	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24142699
1322183	Epm2aip1	EPM2A interacting protein 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24142699
1322183	Epm2aip1	EPM2A interacting protein 1	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24142699
1322185	Cst5	cystatin D	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680148
1322185	Cst5	cystatin D	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680148
1322185	Cst5	cystatin D	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680148
1322185	Cst5	cystatin D	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680148
1322185	Cst5	cystatin D	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680148
1322185	Cst5	cystatin D	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680148
1322187	Thbs2	thrombospondin 2	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213711
1322187	Thbs2	thrombospondin 2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11387198
1322187	Thbs2	thrombospondin 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1322187	Thbs2	thrombospondin 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1322187	Thbs2	thrombospondin 2	gene	MP:0001158	abnormal prostate gland morphology		IEA		N	RGD:5509061	20230119	MGI			
1322187	Thbs2	thrombospondin 2	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213711
1322187	Thbs2	thrombospondin 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1322187	Thbs2	thrombospondin 2	gene	MP:0001391	abnormal tail movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213711
1322187	Thbs2	thrombospondin 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1322187	Thbs2	thrombospondin 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213711
1322187	Thbs2	thrombospondin 2	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1322187	Thbs2	thrombospondin 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1322187	Thbs2	thrombospondin 2	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10571734
1322187	Thbs2	thrombospondin 2	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213711
1322187	Thbs2	thrombospondin 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230119	MGI			
1322187	Thbs2	thrombospondin 2	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213711
1322187	Thbs2	thrombospondin 2	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11387198
1322187	Thbs2	thrombospondin 2	gene	MP:0004958	enlarged prostate gland		IEA		N	RGD:5509061	20230119	MGI			
1322187	Thbs2	thrombospondin 2	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0005504	abnormal ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0005507	tail dragging		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20201002	MGI			PMID:12213711
1322187	Thbs2	thrombospondin 2	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11387198
1322187	Thbs2	thrombospondin 2	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9442117
1322187	Thbs2	thrombospondin 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213711
1322187	Thbs2	thrombospondin 2	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:9442117
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20170928	MGI			
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:11381623
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20170928	MGI			PMID:11381623
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20160728	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IEA		N	RGD:5509061	20170928	MGI			
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001280	loss of vibrissae		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002074	abnormal hair texture		IEA		N	RGD:5509061	20170928	MGI			
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002991	abnormal sebaceous gland physiology		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002991	abnormal sebaceous gland physiology		IAGP		N	RGD:5509061	20170928	MGI			PMID:11381623
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20170928	MGI			PMID:11381623
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20170928	MGI			PMID:11381623
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003875	abnormal hair follicle regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0003981	decreased circulating phospholipid level		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0005081	abnormal dermis reticular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0009545	abnormal dermis papillary layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0009600	hypergranulosis		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0009792	seborrheic dermatitis		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0009793	sebaceous gland hypertrophy		IAGP		N	RGD:5509061	20160728	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0009793	sebaceous gland hypertrophy		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20181129	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0010206	pigment incontinence		IAGP		N	RGD:5509061	20181129	MGI			PMID:12514744
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0010699	dilated hair follicle		IAGP		N	RGD:5509061	20160317	MGI			PMID:15482472
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0013373	increased sebum secretion		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20170608	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20170615	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0030571	dilated piliary canal		IAGP		N	RGD:5509061	20180524	MGI			PMID:24531688
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:23715724
1322188	Mpzl3	myelin protein zero-like 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:23715724
1322190	Trim2	tripartite motif-containing 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20220811	MGI			
1322190	Trim2	tripartite motif-containing 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0003043	hypoalgesia		IEA		N	RGD:5509061	20220519	MGI			
1322190	Trim2	tripartite motif-containing 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322190	Trim2	tripartite motif-containing 2	gene	MP:0009979	abnormal cerebellum deep nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18687884
1322192	Col16a1	collagen, type XVI, alpha 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1322192	Col16a1	collagen, type XVI, alpha 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1322192	Col16a1	collagen, type XVI, alpha 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1322192	Col16a1	collagen, type XVI, alpha 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1322193	Tti1	TELO2 interacting protein 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1322193	Tti1	TELO2 interacting protein 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1322193	Tti1	TELO2 interacting protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20141003	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20160421	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20160421	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20201231	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160421	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20160421	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160421	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0001413	abnormal response to new environment		IEA		N	RGD:5509061	20141003	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20141003	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0004129	abnormal respiratory quotient		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20160421	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20141003	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20141003	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0006241	abnormal placement of pupils		IEA		N	RGD:5509061	20141003	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20160804	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20160421	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20201022	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0011999	abnormal tail length		IEA		N	RGD:5509061	20201231	MGI			
1322200	Cyb561	cytochrome b-561	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20111116	MGI			
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001606	impaired hematopoiesis		IEA		N	RGD:5509061	20161201	MGI			
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20161201	MGI			
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18412166
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16114097
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18412166
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178811
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005000	abnormal immune tolerance		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16114097
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16304053
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20161201	MGI			
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178811
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178811
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008185	decreased naive B cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008191	abnormal follicular B cell physiology		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008202	absent B-1 B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130661
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235209
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723215
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008573	increased circulating interferon-alpha level		IEA		N	RGD:5509061	20161201	MGI			
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18412166
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18412166
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0009548	abnormal platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16011964
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0010187	decreased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826752
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0013940	abnormal plasmablast number		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:12446777
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20161201	MGI			
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0020002	increased response to antigen		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0020175	abnormal IgG1 level		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0020193	increased lymphocyte activation involved in immune response		IAGP		N	RGD:5509061	20250703	MGI			PMID:30127432
1322206	Pik3cd	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20170831	MGI			PMID:22246904
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20170831	MGI			PMID:26989192
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21816367
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20170831	MGI			PMID:22246904
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:22246904
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20171221	MGI			PMID:28504700
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20170831	MGI			PMID:26989192
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170831	MGI			PMID:26989192
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21816367
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20170831	MGI			PMID:22246904
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20170831	MGI			PMID:26989192
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001468	abnormal temporal memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770080
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20171221	MGI			PMID:28504700
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20240718	MGI			PMID:33895792
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20170831	MGI			PMID:26989192
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21816367
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20171221	MGI			PMID:28504700
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0003578	absent ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20170831	MGI			PMID:26989192
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21816367
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770080
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20240718	MGI			PMID:33895792
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20240718	MGI			PMID:33895792
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20240718	MGI			PMID:33895792
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20240718	MGI			PMID:33895792
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0008818	abnormal interfrontal bone morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:22246904
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0008845	abnormal paraventricular hypothalamic nucleus morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:22246904
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0008846	abnormal supraoptic nucleus morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:22246904
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770080
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21816367
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20171221	MGI			PMID:28504700
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770080
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0010343	increased lipoma incidence		IAGP		N	RGD:5509061	20170831	MGI			PMID:22246904
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20171221	MGI			PMID:28504700
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20171221	MGI			PMID:28504700
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20171221	MGI			PMID:28504700
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20171221	MGI			PMID:28504700
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28504700
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20170831	MGI			PMID:26989192
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770080
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0012540	abnormal lamina terminalis morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:22246904
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0013302	increased pancreas iron level		IAGP		N	RGD:5509061	20240718	MGI			PMID:33895792
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0013507	increased ovary apoptosis		IAGP		N	RGD:5509061	20220505	MGI			PMID:23151479
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0013771	decreased effector memory T-helper cell number		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0020385	decreased intestine iron level		IAGP		N	RGD:5509061	20240718	MGI			PMID:33895792
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0030117	bifid nose		IAGP		N	RGD:5509061	20171005	MGI			PMID:26989192
1322210	Tet1	tet methylcytosine dioxygenase 1	gene	MP:0031474	increased female germ cell apoptosis		IAGP		N	RGD:5509061	20230615	MGI			PMID:23151479
1322212	Irf2bpl	interferon regulatory factor 2 binding protein-like	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1322212	Irf2bpl	interferon regulatory factor 2 binding protein-like	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20231207	MGI			
1322212	Irf2bpl	interferon regulatory factor 2 binding protein-like	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1322212	Irf2bpl	interferon regulatory factor 2 binding protein-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1322214	Klk15	kallikrein related-peptidase 15	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20221215	MGI			
1322214	Klk15	kallikrein related-peptidase 15	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20210128	MGI			
1322214	Klk15	kallikrein related-peptidase 15	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210520	MGI			
1322214	Klk15	kallikrein related-peptidase 15	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1322214	Klk15	kallikrein related-peptidase 15	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20210128	MGI			
1322214	Klk15	kallikrein related-peptidase 15	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220519	MGI			
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20141003	MGI			
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001097	abnormal superior glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001101	abnormal superior vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084405
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0003873	pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004266	pale placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004600	abnormal vertebral transverse process morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004602	abnormal vertebral articular process morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004684	intervertebral disk degeneration		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084405
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0005504	abnormal ligament morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0006018	abnormal tympanic membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0006295	absent sclerotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0006320	abnormal interscapular fat pad morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0006393	absent nucleus pulposus		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0008487	abnormal mesonephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20180111	MGI			PMID:24703692
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0009877	exostosis		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0010113	abnormal sacrum morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084405
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150528	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682242
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21666053
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011642	abnormal bone collagen fibril morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0012184	absent paraxial mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0012235	abnormal liver bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0012249	absent myotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0013166	small forelimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0013168	absent hindlimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256345
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0013176	abnormal tail position or orientation		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0014399	decreased hematopoietic precursor cell number		IAGP		N	RGD:5509061	20240321	MGI			PMID:24586749
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0030226	middle ear polyps		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0030410	middle ear effusion		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0030414	tympanic membrane perforation		IAGP		N	RGD:5509061	20171207	MGI			PMID:17029558
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20220929	MGI			PMID:24316420
1322217	Mecom	MDS1 and EVI1 complex locus	gene	MP:0031434	increased miscarriage rate		IAGP		N	RGD:5509061	20220915	MGI			PMID:17029558
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0005356	positive geotaxis		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322219	Pitrm1	pitrilysin metallepetidase 1	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20161222	MGI			PMID:26697887
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130425
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611999
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612000
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0001391	abnormal tail movements		IEA		N	RGD:5509061	20160804	MGI			
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382161
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611999
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612000
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130425
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611999
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130425
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382161
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611999
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612000
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612000
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382161
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611999
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612000
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141009	MGI			PMID:24361012
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0004850	abnormal testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382161
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612000
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382161
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382161
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611999
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612000
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382161
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382161
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130425
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22084409
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141009	MGI			PMID:24361012
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612000
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0009839	multiflagellated sperm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16612000
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20141009	MGI			PMID:24361012
1322221	Cadm1	cell adhesion molecule 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:18055550
1322223	Spmip6	sperm microtubule inner protein 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1322224	A2ml1	alpha-2-macroglobulin like 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1322224	A2ml1	alpha-2-macroglobulin like 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1322224	A2ml1	alpha-2-macroglobulin like 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201022	MGI			
1322225	Pfn3	profilin 3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0030949	abnormal Golgi vesicle transport		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322225	Pfn3	profilin 3	gene	MP:0031374	abnormal manchette assembly		IAGP		N	RGD:5509061	20220407	MGI			PMID:34869336
1322229	Ift52	intraflagellar transport 52	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20201022	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20201022	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20201022	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20201022	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322229	Ift52	intraflagellar transport 52	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1322232	C1qtnf4	C1q and tumor necrosis factor related protein 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1322232	C1qtnf4	C1q and tumor necrosis factor related protein 4	gene	MP:0008113	abnormal macrophage differentiation		IAGP		N	RGD:5509061	20210819	MGI			PMID:33080044
1322232	C1qtnf4	C1q and tumor necrosis factor related protein 4	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20210819	MGI			PMID:33080044
1322232	C1qtnf4	C1q and tumor necrosis factor related protein 4	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20210819	MGI			PMID:33080044
1322232	C1qtnf4	C1q and tumor necrosis factor related protein 4	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20210819	MGI			PMID:33080044
1322232	C1qtnf4	C1q and tumor necrosis factor related protein 4	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20210819	MGI			PMID:33080044
1322232	C1qtnf4	C1q and tumor necrosis factor related protein 4	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20210819	MGI			PMID:33080044
1322232	C1qtnf4	C1q and tumor necrosis factor related protein 4	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210819	MGI			PMID:33080044
1322233	Myo18a	myosin XVIIIA	gene	MP:0000603	pale liver		IEA		N	RGD:5509061	20210520	MGI			
1322233	Myo18a	myosin XVIIIA	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1322233	Myo18a	myosin XVIIIA	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1322233	Myo18a	myosin XVIIIA	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1322233	Myo18a	myosin XVIIIA	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:30737279
1322233	Myo18a	myosin XVIIIA	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:30737279
1322233	Myo18a	myosin XVIIIA	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20160811	MGI			
1322233	Myo18a	myosin XVIIIA	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20160811	MGI			
1322233	Myo18a	myosin XVIIIA	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:30737279
1322233	Myo18a	myosin XVIIIA	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:30737279
1322233	Myo18a	myosin XVIIIA	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:30737279
1322233	Myo18a	myosin XVIIIA	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20191003	MGI			PMID:30737279
1322233	Myo18a	myosin XVIIIA	gene	MP:0030566	abnormal A band morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:30737279
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20200402	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20160804	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0000322	increased granulocyte number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20160114	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20200402	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20200402	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0003884	decreased macrophage cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0004974	decreased regulatory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20160804	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20160804	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008127	decreased dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008346	increased gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0009926	decreased transitional stage T2 B cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0010093	decreased circulating magnesium level		IEA		N	RGD:5509061	20210128	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0012768	decreased KLRG1-positive NK cell number		IEA		N	RGD:5509061	20160804	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013155	decreased KLRG1+ CD8-positive alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013427	increased memory-marker NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013429	decreased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013430	increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013511	increased CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013513	decreased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013519	decreased CD4-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013522	decreased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013667	increased immature NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013672	decreased mature NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013675	decreased Ly6C-positive mature NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013679	increased Ly6C-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1322235	Gmds	GDP-mannose 4, 6-dehydratase	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1322238	Cradd	CASP2 and RIPK1 domain containing adaptor with death domain	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16183742
1322238	Cradd	CASP2 and RIPK1 domain containing adaptor with death domain	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16183742
1322238	Cradd	CASP2 and RIPK1 domain containing adaptor with death domain	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15865046
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0000098	abnormal vomer bone morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0004134	abnormal chest morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0005227	abnormal vertebral body development		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322240	Loxl3	lysyl oxidase-like 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160310	MGI			PMID:26307084
1322244	Tbx2	T-box 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22130515
1322244	Tbx2	T-box 2	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22130515
1322244	Tbx2	T-box 2	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19769959
1322244	Tbx2	T-box 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19769959
1322244	Tbx2	T-box 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095052
1322244	Tbx2	T-box 2	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22130515
1322244	Tbx2	T-box 2	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095052
1322244	Tbx2	T-box 2	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0009382	abnormal cardiac jelly morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22130515
1322244	Tbx2	T-box 2	gene	MP:0009744	postaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095052
1322244	Tbx2	T-box 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19769959
1322244	Tbx2	T-box 2	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0010587	conotruncal ridge hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19769959
1322244	Tbx2	T-box 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095052
1322244	Tbx2	T-box 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0013917	persistent right 6th pharyngeal arch artery		IAGP		N	RGD:5509061	20191219	MGI			PMID:15459098
1322244	Tbx2	T-box 2	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20220721	MGI			PMID:19769959
1322244	Tbx2	T-box 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:19769959
1322244	Tbx2	T-box 2	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:19769959
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230601	MGI			
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20230601	MGI			
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230601	MGI			
1322246	Gramd2b	GRAM domain containing 2B	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230601	MGI			
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084255
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220519	MGI			
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0001525	impaired balance		IEA		N	RGD:5509061	20120105	MGI			
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220519	MGI			
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084255
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220519	MGI			
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0010745	abnormal pre-Botzinger complex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0010746	abnormal pre-Botzinger complex physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0011042	abnormal horizontal vestibuloocular reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20680010
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084255
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0014647	decreased horizontal optokinetic reflex		IAGP		N	RGD:5509061	20250306	MGI			PMID:20231872
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0014751	abnormal commissural neuron axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:15084255
1322249	Robo3	roundabout guidance receptor 3	gene	MP:0021092	abnormal dorsal interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:18701067
1322252	Arpin	actin-related protein 2/3 complex inhibitor	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20250515	MGI			PMID:39298260
1322252	Arpin	actin-related protein 2/3 complex inhibitor	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20250515	MGI			PMID:39298260
1322252	Arpin	actin-related protein 2/3 complex inhibitor	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20250515	MGI			PMID:39298260
1322252	Arpin	actin-related protein 2/3 complex inhibitor	gene	MP:0004125	abnormal venule morphology		IAGP		N	RGD:5509061	20250515	MGI			PMID:39298260
1322252	Arpin	actin-related protein 2/3 complex inhibitor	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20250515	MGI			PMID:39298260
1322252	Arpin	actin-related protein 2/3 complex inhibitor	gene	MP:0010909	pulmonary alveolar hemorrhage		IAGP		N	RGD:5509061	20250515	MGI			PMID:39298260
1322256	Dysf	dysferlin	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20210429	MGI			PMID:30292141
1322256	Dysf	dysferlin	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21060153
1322256	Dysf	dysferlin	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508505
1322256	Dysf	dysferlin	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508505
1322256	Dysf	dysferlin	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736685
1322256	Dysf	dysferlin	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22666441
1322256	Dysf	dysferlin	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1322256	Dysf	dysferlin	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20210429	MGI			PMID:30292141
1322256	Dysf	dysferlin	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254015
1322256	Dysf	dysferlin	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1322256	Dysf	dysferlin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254015
1322256	Dysf	dysferlin	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20210429	MGI			PMID:30292141
1322256	Dysf	dysferlin	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20210429	MGI			PMID:30292141
1322256	Dysf	dysferlin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254015
1322256	Dysf	dysferlin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1322256	Dysf	dysferlin	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20161216	MGI			PMID:21060153
1322256	Dysf	dysferlin	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736685
1322256	Dysf	dysferlin	gene	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254015
1322256	Dysf	dysferlin	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1322256	Dysf	dysferlin	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20161216	MGI			PMID:21060153
1322256	Dysf	dysferlin	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254015
1322256	Dysf	dysferlin	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736685
1322256	Dysf	dysferlin	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1322256	Dysf	dysferlin	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20161216	MGI			PMID:21060153
1322256	Dysf	dysferlin	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736685
1322256	Dysf	dysferlin	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254015
1322256	Dysf	dysferlin	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1322256	Dysf	dysferlin	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20161216	MGI			PMID:21060153
1322256	Dysf	dysferlin	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736685
1322256	Dysf	dysferlin	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254015
1322256	Dysf	dysferlin	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1322256	Dysf	dysferlin	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736685
1322256	Dysf	dysferlin	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254015
1322256	Dysf	dysferlin	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1322256	Dysf	dysferlin	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20210429	MGI			PMID:30292141
1322256	Dysf	dysferlin	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20160114	MGI			PMID:25198651
1322256	Dysf	dysferlin	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20161216	MGI			PMID:21060153
1322256	Dysf	dysferlin	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20210429	MGI			PMID:30292141
1322256	Dysf	dysferlin	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254015
1322256	Dysf	dysferlin	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12736685
1322256	Dysf	dysferlin	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20161216	MGI			PMID:21060153
1322256	Dysf	dysferlin	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:12736685
1322256	Dysf	dysferlin	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1322258	Pum2	pumilio RNA-binding family member 2	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17219433
1322258	Pum2	pumilio RNA-binding family member 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1322258	Pum2	pumilio RNA-binding family member 2	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20231207	MGI			
1322258	Pum2	pumilio RNA-binding family member 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1322258	Pum2	pumilio RNA-binding family member 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17219433
1322258	Pum2	pumilio RNA-binding family member 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1322258	Pum2	pumilio RNA-binding family member 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1322260	Fam53c	family with sequence similarity 53, member C	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1322261	Tkfc	triokinase, FMN cyclase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1322261	Tkfc	triokinase, FMN cyclase	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1322261	Tkfc	triokinase, FMN cyclase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1322261	Tkfc	triokinase, FMN cyclase	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1322261	Tkfc	triokinase, FMN cyclase	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1322261	Tkfc	triokinase, FMN cyclase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1322261	Tkfc	triokinase, FMN cyclase	gene	MP:0001330	abnormal optic nerve morphology		IEA		N	RGD:5509061	20230601	MGI			
1322261	Tkfc	triokinase, FMN cyclase	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20230601	MGI			
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20210128	MGI			
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322264	Arhgap21	Rho GTPase activating protein 21	gene	MP:0020463	increased megakaryocyte progenitor cell number		IAGP		N	RGD:5509061	20180913	MGI			PMID:29212046
1322267	Tmod3	tropomodulin 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0011176	abnormal erythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:24159174
1322267	Tmod3	tropomodulin 3	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:24159174
1322271	Cst9	cystatin 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923608
1322271	Cst9	cystatin 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427609
1322271	Cst9	cystatin 9	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
1322271	Cst9	cystatin 9	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20170105	MGI			
1322273	Ppp1r16b	protein phosphatase 1, regulatory subunit 16B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17683113
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0000192	abnormal mineral level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:19136963
1322275	Ethe1	ethylmalonic encephalopathy 1	gene	MP:0014970	decreased muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19136963
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0011321	abnormal peritubular capillary morphology		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0011444	abnormal renal water homeostasis		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0011454	abnormal glomerular endothelium fenestra morphology		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0011856	abnormal glomerular filtration barrier function		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322278	Zfyve21	zinc finger, FYVE domain containing 21	gene	MP:0013285	abnormal renal filtration		IAGP		N	RGD:5509061	20240829	MGI			PMID:38797325
1322280	Crls1	cardiolipin synthase 1	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322280	Crls1	cardiolipin synthase 1	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322280	Crls1	cardiolipin synthase 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322280	Crls1	cardiolipin synthase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322280	Crls1	cardiolipin synthase 1	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0014396	decreased fat cell mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:29861389
1322280	Crls1	cardiolipin synthase 1	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20210729	MGI			PMID:29861389
1322282	Saxo1	stabilizer of axonemal microtubules 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1322282	Saxo1	stabilizer of axonemal microtubules 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1322282	Saxo1	stabilizer of axonemal microtubules 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210506	MGI			PMID:32814578
1322282	Saxo1	stabilizer of axonemal microtubules 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20211021	MGI			
1322282	Saxo1	stabilizer of axonemal microtubules 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1322282	Saxo1	stabilizer of axonemal microtubules 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10205062
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267005
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23946405
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14985318
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752778
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123450
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3417421
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752778
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15184660
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123450
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267005
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387789
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23946405
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14985318
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123450
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267005
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123450
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23946405
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8638127
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5009246
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10205062
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:864040
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23946405
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980879
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23946405
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980879
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26392540
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3417421
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980879
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213800
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267005
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23946405
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8638127
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0006149	decreased visual acuity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123450
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0006243	impaired pupillary reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522242
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0006243	impaired pupillary reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18545654
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123450
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387789
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23946405
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:3417421
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267005
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14985318
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008454	absent retina rod cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008454	absent retina rod cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16576828
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752778
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387789
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16123450
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:3417421
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008517	thick retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:14985318
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267005
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:3005510
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980879
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008520	disorganized retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11980879
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:3417421
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160114	MGI			PMID:25477496
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23946405
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0011279	decreased ear pigmentation		IAGP		N	RGD:5509061	20170803	MGI			PMID:864040
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0011831	abnormal visual contrast sensitivity		IAGP		N	RGD:5509061	20151119	MGI			PMID:22633808
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:3417421
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0020442	serous retina detachment		IAGP		N	RGD:5509061	20170907	MGI			PMID:26978024
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:11114194
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20171012	MGI			PMID:18545654
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20171012	MGI			PMID:11114194
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0031139	abnormal retina artery morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33539865
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:11929848
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:16123450
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:17213800
1322284	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:17267005
1322286	Gbp5	guanylate binding protein 5	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461501
1322286	Gbp5	guanylate binding protein 5	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461501
1322286	Gbp5	guanylate binding protein 5	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461501
1322286	Gbp5	guanylate binding protein 5	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461501
1322286	Gbp5	guanylate binding protein 5	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461501
1322286	Gbp5	guanylate binding protein 5	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461501
1322288	Arid5a	AT-rich interaction domain 5A	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23676272
1322288	Arid5a	AT-rich interaction domain 5A	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23676272
1322288	Arid5a	AT-rich interaction domain 5A	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23676272
1322288	Arid5a	AT-rich interaction domain 5A	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23676272
1322288	Arid5a	AT-rich interaction domain 5A	gene	MP:0010220	decreased T-helper 17 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23676272
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21536732
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510201
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21536732
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914746
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914746
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914746
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510201
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914746
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914746
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0003338	pancreas lipomatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510201
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510201
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510201
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305640
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0008805	decreased circulating amylase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510201
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510201
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0009154	pancreatic acinar hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510201
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0009170	abnormal pancreatic islet size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510201
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21536732
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21536732
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914746
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IEA		N	RGD:5509061	20230615	MGI			
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0011198	absent proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914746
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914746
1322291	Sbds	SBDS ribosome maturation factor	gene	MP:0014242	abnormal ribosome biogenesis		IEA		N	RGD:5509061	20230622	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20231207	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20231207	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0002743	glomerulonephritis		IEA		N	RGD:5509061	20141003	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20231207	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20231207	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20231207	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20141003	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20231207	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0008470	abnormal spleen B cell follicle morphology		IEA		N	RGD:5509061	20141003	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16684884
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20231207	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1322293	Gnb1l	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20160804	MGI			
1322296	Tmprss15	transmembrane protease, serine 15	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1322299	Rnf7	ring finger protein 7	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24430184
1322299	Rnf7	ring finger protein 7	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24430184
1322299	Rnf7	ring finger protein 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24430184
1322299	Rnf7	ring finger protein 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1322299	Rnf7	ring finger protein 7	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20160804	MGI			
1322299	Rnf7	ring finger protein 7	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20160804	MGI			
1322299	Rnf7	ring finger protein 7	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20638939
1322299	Rnf7	ring finger protein 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20638939
1322299	Rnf7	ring finger protein 7	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0005316	abnormal response to tactile stimuli		IEA		N	RGD:5509061	20141003	MGI			
1322299	Rnf7	ring finger protein 7	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20638939
1322299	Rnf7	ring finger protein 7	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24430184
1322299	Rnf7	ring finger protein 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0013182	increased spinal cord apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:22118770
1322299	Rnf7	ring finger protein 7	gene	MP:0013551	decreased cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20161201	MGI			PMID:24210661
1322299	Rnf7	ring finger protein 7	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:24210661
1322304	Nup160	nucleoporin 160	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20210722	MGI			PMID:32988961
1322304	Nup160	nucleoporin 160	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20210722	MGI			PMID:32988961
1322307	Gins2	GINS complex subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1322307	Gins2	GINS complex subunit 2	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1322309	Eef1e1	eukaryotic translation elongation factor 1 epsilon 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680327
1322309	Eef1e1	eukaryotic translation elongation factor 1 epsilon 1	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680327
1322309	Eef1e1	eukaryotic translation elongation factor 1 epsilon 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680327
1322309	Eef1e1	eukaryotic translation elongation factor 1 epsilon 1	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680327
1322309	Eef1e1	eukaryotic translation elongation factor 1 epsilon 1	gene	MP:0009341	decreased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680327
1322309	Eef1e1	eukaryotic translation elongation factor 1 epsilon 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680327
1322309	Eef1e1	eukaryotic translation elongation factor 1 epsilon 1	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680327
1322311	Brms1	breast cancer metastasis-suppressor 1	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1322311	Brms1	breast cancer metastasis-suppressor 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1322311	Brms1	breast cancer metastasis-suppressor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0002804	abnormal motor learning		IEA		N	RGD:5509061	20210520	MGI			
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0003440	decreased glycerol level		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0003978	decreased circulating carnitine level		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0006038	increased mitochondrial fission		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0014174	decreased fatty acid beta-oxidation		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0014775	decreased skeletal muscle enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0030612	organic aciduria		IAGP		N	RGD:5509061	20191128	MGI			PMID:31480808
1322313	Adck2	aarF domain containing kinase 2	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:31480808
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20231207	MGI			
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0010187	decreased T follicular helper cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20231207	MGI			
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0013705	decreased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0013771	decreased effector memory T-helper cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322316	Ctps1	cytidine 5'-triphosphate synthase 1	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1322320	Tulp1	TUB like protein 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481257
1322320	Tulp1	TUB like protein 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20150129	MGI			PMID:21052544
1322320	Tulp1	TUB like protein 1	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20210916	MGI			PMID:22323461
1322320	Tulp1	TUB like protein 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481257
1322320	Tulp1	TUB like protein 1	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0005551	abnormal eye electrophysiology		IEA		N	RGD:5509061	20220113	MGI			
1322320	Tulp1	TUB like protein 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481257
1322320	Tulp1	TUB like protein 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
1322320	Tulp1	TUB like protein 1	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481257
1322320	Tulp1	TUB like protein 1	gene	MP:0008583	absent photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20150129	MGI			PMID:22183357
1322320	Tulp1	TUB like protein 1	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481257
1322320	Tulp1	TUB like protein 1	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220113	MGI			
1322320	Tulp1	TUB like protein 1	gene	MP:0010749	absent visual evoked potential		IEA		N	RGD:5509061	20220113	MGI			
1322320	Tulp1	TUB like protein 1	gene	MP:0012671	retina spots		IEA		N	RGD:5509061	20220113	MGI			
1322320	Tulp1	TUB like protein 1	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:10607826
1322320	Tulp1	TUB like protein 1	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:10607826
1322321	Virma	vir like m6A methyltransferase associated	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322321	Virma	vir like m6A methyltransferase associated	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322321	Virma	vir like m6A methyltransferase associated	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322321	Virma	vir like m6A methyltransferase associated	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322324	Tekt2	tektin 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340058
1322324	Tekt2	tektin 2	gene	MP:0001947	abnormal mucociliary clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340058
1322324	Tekt2	tektin 2	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340058
1322324	Tekt2	tektin 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340058
1322324	Tekt2	tektin 2	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340058
1322324	Tekt2	tektin 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340058
1322324	Tekt2	tektin 2	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340058
1322324	Tekt2	tektin 2	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340058
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0004062	dilated heart right atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322328	Srsf10	serine and arginine-rich splicing factor 10	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19386262
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284245
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15188439
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15188439
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15188439
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15188439
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0001432	abnormal food preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:15188439
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15188439
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15188439
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284245
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0002243	abnormal vomeronasal organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452247
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285371
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22678282
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284245
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20250508	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284245
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452247
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0008228	increased anterior commissure size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20250508	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20260402	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0011679	abnormal vomeronasal sensory neuron morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:21452247
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20260402	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0012484	decreased corticospinal tract size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0013595	absent vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:21452247
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0013597	small vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:21452247
1322329	Fezf2	Fez family zinc finger 2	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:16971467
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18416604
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19201855
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18416604
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18416604
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000613	abnormal salivary gland morphology		IEA		N	RGD:5509061	20260402	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20150101	MGI			PMID:24711413
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20241121	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20241121	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20241121	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18416604
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20250508	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611229
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002397	abnormal bone marrow morphology		IEA		N	RGD:5509061	20241121	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18416604
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611229
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630375
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:24711413
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:8073287
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19201855
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20250508	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18416604
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19201855
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8073287
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630375
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20150101	MGI			PMID:24711413
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20210304	MGI			PMID:25636339
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20241121	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630375
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20210304	MGI			PMID:25636339
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18416604
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20150101	MGI			PMID:24711413
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:24711413
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0008253	absent megakaryocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8073287
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0008253	absent megakaryocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8630375
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20150101	MGI			PMID:24711413
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20150101	MGI			PMID:24711413
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0009516	enlarged salivary gland		IEA		N	RGD:5509061	20260402	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059699
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20260402	MGI			
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18416604
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20150101	MGI			PMID:24711413
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0014348	decreased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:15071178
1322331	Mpl	Mpl proto-oncogene, thrombopoietin receptor	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:15071178
1322334	Recql	RecQ protein-like	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158923
1322334	Recql	RecQ protein-like	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158923
1322334	Recql	RecQ protein-like	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158923
1322334	Recql	RecQ protein-like	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158923
1322334	Recql	RecQ protein-like	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158923
1322336	Rtf2	replication termination factor 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250130	MGI			PMID:38431617
1322336	Rtf2	replication termination factor 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20250130	MGI			PMID:38431617
1322336	Rtf2	replication termination factor 2	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20250130	MGI			PMID:38431617
1322336	Rtf2	replication termination factor 2	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20250130	MGI			PMID:38431617
1322338	Poldip3	polymerase (DNA-directed), delta interacting protein 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1322338	Poldip3	polymerase (DNA-directed), delta interacting protein 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1322338	Poldip3	polymerase (DNA-directed), delta interacting protein 3	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20240523	MGI			
1322341	Psd2	pleckstrin and Sec7 domain containing 2	gene	MP:0020360	abnormal asymmetric synapse morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31095630
1322342	Klhl29	kelch-like 29	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1322342	Klhl29	kelch-like 29	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20210128	MGI			
1322342	Klhl29	kelch-like 29	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20210128	MGI			
1322342	Klhl29	kelch-like 29	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20211021	MGI			
1322342	Klhl29	kelch-like 29	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20210128	MGI			
1322342	Klhl29	kelch-like 29	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322342	Klhl29	kelch-like 29	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0014523	increased response to brain injury		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322343	Fam76b	family with sequence similarity 76, member B	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20241128	MGI			PMID:37643469
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0004126	thin hypodermis		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0008800	increased small intestinal crypt cell apoptosis		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0010207	abnormal telomere morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0013660	abnormal bone marrow hematopoietic cell morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0013776	bone marrow failure		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0014078	small intestinal villus atrophy		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0014508	decreased intestinal crypt stem cell number		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0030926	increased skin pigmentation		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322344	Ten1	TEN1 telomerase capping complex subunit	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20250605	MGI			PMID:40215293
1322346	Lgi3	leucine-rich repeat LGI family, member 3	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1322346	Lgi3	leucine-rich repeat LGI family, member 3	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20210128	MGI			
1322346	Lgi3	leucine-rich repeat LGI family, member 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1322346	Lgi3	leucine-rich repeat LGI family, member 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1322346	Lgi3	leucine-rich repeat LGI family, member 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1322346	Lgi3	leucine-rich repeat LGI family, member 3	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1322346	Lgi3	leucine-rich repeat LGI family, member 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1322346	Lgi3	leucine-rich repeat LGI family, member 3	gene	MP:0010737	abnormal juxtaparanode morphology		IAGP		N	RGD:5509061	20220908	MGI			PMID:35948005
1322346	Lgi3	leucine-rich repeat LGI family, member 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230330	MGI			PMID:36828548
1322349	Ndufs5	NADH:ubiquinone oxidoreductase core subunit S5	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230601	MGI			
1322349	Ndufs5	NADH:ubiquinone oxidoreductase core subunit S5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1322351	Atp6v1c1	ATPase, H+ transporting, lysosomal V1 subunit C1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1322351	Atp6v1c1	ATPase, H+ transporting, lysosomal V1 subunit C1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1322351	Atp6v1c1	ATPase, H+ transporting, lysosomal V1 subunit C1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20181227	MGI			
1322351	Atp6v1c1	ATPase, H+ transporting, lysosomal V1 subunit C1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20170105	MGI			
1322351	Atp6v1c1	ATPase, H+ transporting, lysosomal V1 subunit C1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1322351	Atp6v1c1	ATPase, H+ transporting, lysosomal V1 subunit C1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322351	Atp6v1c1	ATPase, H+ transporting, lysosomal V1 subunit C1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0010059	olfactory bulb hypoplasia		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0013551	decreased cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322352	Chmp1a	charged multivesicular body protein 1A	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20210415	MGI			PMID:30044992
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166380
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821749
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808090
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821749
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808090
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821749
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821749
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821749
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821749
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166380
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003153	early eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166380
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003819	increased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821749
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0005439	decreased glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821749
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15821749
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0008816	petechiae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166380
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17571162
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923692
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10779359
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808090
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0012185	abnormal muscle precursor cell morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:17881575
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995442
1322355	Gab1	growth factor receptor bound protein 2-associated protein 1	gene	MP:0030208	abnormal intrinsic tongue muscle morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:16166380
1322360	Peg3	paternally expressed 3	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195900
1322360	Peg3	paternally expressed 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141218	MGI			PMID:24391757
1322360	Peg3	paternally expressed 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22394678
1322360	Peg3	paternally expressed 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195900
1322360	Peg3	paternally expressed 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22394678
1322360	Peg3	paternally expressed 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141218	MGI			PMID:24391757
1322360	Peg3	paternally expressed 3	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195900
1322360	Peg3	paternally expressed 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141218	MGI			PMID:24391757
1322360	Peg3	paternally expressed 3	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195900
1322360	Peg3	paternally expressed 3	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:22394678
1322360	Peg3	paternally expressed 3	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141218	MGI			PMID:24391757
1322360	Peg3	paternally expressed 3	gene	MP:0009326	absent maternal crouching		IAGP		N	RGD:5509061	20141003	MGI			PMID:10195900
1322360	Peg3	paternally expressed 3	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141218	MGI			PMID:24391757
1322360	Peg3	paternally expressed 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141218	MGI			PMID:24391757
1322360	Peg3	paternally expressed 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22394678
1322362	Stoml3	stomatin (Epb7.2)-like 3	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167420
1322362	Stoml3	stomatin (Epb7.2)-like 3	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167420
1322362	Stoml3	stomatin (Epb7.2)-like 3	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167420
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20190502	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20190502	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20190502	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20201022	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20241121	MGI			
1322364	Tedc1	tubulin epsilon and delta complex 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20201105	MGI			PMID:31671076
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201105	MGI			PMID:31671076
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:31671076
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:31671076
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20201105	MGI			PMID:31671076
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0009425	increased soleus weight		IAGP		N	RGD:5509061	20201105	MGI			PMID:31671076
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0009426	decreased soleus weight		IAGP		N	RGD:5509061	20201105	MGI			PMID:31671076
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0010226	increased quadriceps weight		IAGP		N	RGD:5509061	20201105	MGI			PMID:31671076
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1322366	Kbtbd13	kelch repeat and BTB (POZ) domain containing 13	gene	MP:0012059	thick diaphragm muscle		IAGP		N	RGD:5509061	20201105	MGI			PMID:31671076
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0001329	retina hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20240822	MGI			PMID:37144879
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003005	abnormal hippocampal fimbria morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003006	abnormal hippocampal fornix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003557	absent vas deferens		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003558	absent uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003575	absent oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003578	absent ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004171	abnormal pallium development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004318	absent incus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004318	absent incus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004417	decreased cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004727	absent epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004729	absent efferent ductules of testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004739	conductive hearing loss		IEA		N	RGD:5509061	20141003	MGI			
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004740	sensorineural hearing loss		IEA		N	RGD:5509061	20141003	MGI			
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004750	syndromic hearing loss		IEA		N	RGD:5509061	20141003	MGI			
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004767	increased cochlear nerve compound action potential		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0005644	agonadal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0006415	absent testes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0006425	absent Mullerian ducts		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0008262	abnormal hippocampus region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20161103	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009048	enlarged tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009072	absent cranial vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009074	Wolffian duct degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009206	absent internal male genitalia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009210	absent internal female genitalia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009324	absent hippocampal fimbria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009324	absent hippocampal fimbria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009637	abnormal pretectal region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009637	abnormal pretectal region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0010893	abnormal posterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011412	gonadal ridge hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011457	abnormal metanephric ureteric bud development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0011760	abnormal ureteric bud tip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9165114
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493561
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:15201223
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:15917450
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0020545	decreased hippocampal fornix size		IAGP		N	RGD:5509061	20180301	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0030108	abnormal incudostapedial joint morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0030109	abnormal incudomalleolar joint morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:9012509
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0030109	abnormal incudomalleolar joint morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0030396	abnormal incus long process morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0030398	absent incus lenticular process		IAGP		N	RGD:5509061	20171207	MGI			PMID:15044845
1322368	Emx2	empty spiracles homeobox 2	gene	MP:0030402	abnormal stapes head morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:15044845
1322373	Ctr9	CTR9 homolog, Paf1/RNA polymerase II complex component	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1322373	Ctr9	CTR9 homolog, Paf1/RNA polymerase II complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322373	Ctr9	CTR9 homolog, Paf1/RNA polymerase II complex component	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322373	Ctr9	CTR9 homolog, Paf1/RNA polymerase II complex component	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000026	abnormal inner ear morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000079	abnormal basioccipital bone morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000106	abnormal basisphenoid bone morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000141	abnormal vertebral body morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20150430	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000297	abnormal atrioventricular cushion morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000632	abnormal pineal gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000690	absent spleen		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000694	spleen hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000819	abnormal olfactory bulb morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0000964	small dorsal root ganglion		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001014	absent superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001062	absent oculomotor nerve		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001075	abnormal accessory nerve morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0002237	abnormal nasal cavity morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0002239	abnormal nasal septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0003056	abnormal hyoid bone morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0003327	liver cyst		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0003584	bifid ureter		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0003755	abnormal palate morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0003888	liver hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004110	transposition of great arteries		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004181	abnormal carotid artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004574	broad limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004668	absent vertebral body		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0004950	abnormal brain vasculature morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0005157	holoprosencephaly		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0005358	abnormal incisor morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0006065	abnormal heart position or orientation		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0008129	absent brain internal capsule		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0008320	absent adenohypophysis		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0008461	left atrial isomerism		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0009526	absent sublingual gland		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0009570	abnormal right lung morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0009771	absent optic chiasm		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0009907	decreased tongue size		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0010403	atrial septal defect		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0010406	common atrium		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20150917	MGI			PMID:23469020
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20150917	MGI			PMID:23469020
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0010427	double outlet left ventricle		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0010431	atrial situs inversus		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0010440	anomalous pulmonary venous connection		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0010572	persistent right dorsal aorta		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553904
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0011250	abdominal situs ambiguus		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0011759	absent Rathke's pouch		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0012730	abnormal internal carotid artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013186	abnormal basilar artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013247	placenta necrosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013349	small Rathke's pouch		IAGP		N	RGD:5509061	20141218	MGI			PMID:17558409
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013828	thin facial nerve		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013830	abnormal intrathoracic topology of vagus nerve		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013852	abnormal Mullerian duct topology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013853	abnormal hepatic portal vein formation		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013858	abnormal azygos vein topology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013861	abnormal pancreas topology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013867	abnormal ventral pancreas morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013878	abnormal ductus venosus valve topology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013914	absent intracranial segment of vertebral artery		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013917	persistent right 6th pharyngeal arch artery		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013928	thin motoric part of trigeminal nerve		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013952	retroesophageal left subclavian artery		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013975	abnormal coronary sinus connection		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013977	symmetric azygos veins		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013979	abnormal subclavian artery origin		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013982	inverse situs of great intrathoracic arteries		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013985	abnormal umbilical vein topology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013987	absent intrahepatic inferior vena cava segment		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013996	abnormal vertebral artery origin		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013997	abnormal internal carotid artery topology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013998	absent canalicular internal carotid artery segment		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0013999	absent parasellar internal carotid artery		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0014000	anastomosis between internal carotid artery and basilar artery		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0014012	abnormal cranial blood vasculature morphology		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0014023	abnormal intestine placement		IEA		N	RGD:5509061	20170504	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0020485	abnormal inferior vena cava topology		IEA		N	RGD:5509061	20180628	MGI			
1322375	Rpgrip1l	Rpgrip1-like	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:29539633
1322376	Slc51a	solute carrier family 51, alpha subunit	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292224
1322376	Slc51a	solute carrier family 51, alpha subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17650074
1322376	Slc51a	solute carrier family 51, alpha subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292224
1322376	Slc51a	solute carrier family 51, alpha subunit	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292224
1322376	Slc51a	solute carrier family 51, alpha subunit	gene	MP:0003947	abnormal cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292224
1322376	Slc51a	solute carrier family 51, alpha subunit	gene	MP:0004774	abnormal bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292224
1322376	Slc51a	solute carrier family 51, alpha subunit	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292224
1322376	Slc51a	solute carrier family 51, alpha subunit	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292224
1322376	Slc51a	solute carrier family 51, alpha subunit	gene	MP:0014480	increased feces cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18292224
1322378	Cda	cytidine deaminase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20230406	MGI			PMID:36496104
1322378	Cda	cytidine deaminase	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20230406	MGI			PMID:36496104
1322378	Cda	cytidine deaminase	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20230406	MGI			PMID:36496104
1322378	Cda	cytidine deaminase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20230406	MGI			PMID:36496104
1322378	Cda	cytidine deaminase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20230406	MGI			PMID:36496104
1322378	Cda	cytidine deaminase	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20230406	MGI			PMID:36496104
1322381	Ooep	oocyte expressed protein	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18804437
1322381	Ooep	oocyte expressed protein	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18804437
1322381	Ooep	oocyte expressed protein	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20590823
1322381	Ooep	oocyte expressed protein	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1322381	Ooep	oocyte expressed protein	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18804437
1322381	Ooep	oocyte expressed protein	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20590823
1322381	Ooep	oocyte expressed protein	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1322381	Ooep	oocyte expressed protein	gene	MP:0020850	abnormal microtubule cytoskeleton morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0010419	inlet ventricular septal defect		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322384	Arid2	AT-rich interaction domain 2	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20160324	MGI			PMID:25299188
1322386	Olfml3	olfactomedin-like 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172977
1322399	Strap	serine/threonine kinase receptor associated protein	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981515
1322399	Strap	serine/threonine kinase receptor associated protein	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981515
1322399	Strap	serine/threonine kinase receptor associated protein	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981515
1322399	Strap	serine/threonine kinase receptor associated protein	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981515
1322399	Strap	serine/threonine kinase receptor associated protein	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981515
1322399	Strap	serine/threonine kinase receptor associated protein	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20181206	MGI			PMID:28827371
1322399	Strap	serine/threonine kinase receptor associated protein	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14981515
1322401	Ap3s1	adaptor-related protein complex 3, sigma 1 subunit	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1322401	Ap3s1	adaptor-related protein complex 3, sigma 1 subunit	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980352
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447442
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690042
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447442
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690042
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447441
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447441
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447442
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0008561	decreased tumor necrosis factor secretion		IEA		N	RGD:5509061	20111116	MGI			
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148800
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:21148800
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690042
1322403	Tirap	toll-interleukin 1 receptor (TIR) domain-containing adaptor protein	gene	MP:0031704	decreased interferon type I secretion		IEA		N	RGD:5509061	20260402	MGI			
1322404	Unc79	unc-79 homolog	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1322404	Unc79	unc-79 homolog	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1322404	Unc79	unc-79 homolog	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0002849	abnormal saccharin consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0002850	saccharin preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1322404	Unc79	unc-79 homolog	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1322404	Unc79	unc-79 homolog	gene	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0009778	impaired behavioral response to anesthetic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1322404	Unc79	unc-79 homolog	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1322404	Unc79	unc-79 homolog	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:20714347
1322404	Unc79	unc-79 homolog	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:16436185
1322407	Prdm13	PR domain containing 13	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1322407	Prdm13	PR domain containing 13	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20160728	MGI			PMID:25995483
1322407	Prdm13	PR domain containing 13	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1322407	Prdm13	PR domain containing 13	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20160728	MGI			PMID:25995483
1322407	Prdm13	PR domain containing 13	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20160728	MGI			PMID:25995483
1322407	Prdm13	PR domain containing 13	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20160728	MGI			PMID:25995483
1322407	Prdm13	PR domain containing 13	gene	MP:0011831	abnormal visual contrast sensitivity		IAGP		N	RGD:5509061	20160728	MGI			PMID:25995483
1322407	Prdm13	PR domain containing 13	gene	MP:0014642	increased optokinetic reflex		IAGP		N	RGD:5509061	20250306	MGI			PMID:25995483
1322409	Med17	mediator complex subunit 17	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1322409	Med17	mediator complex subunit 17	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322409	Med17	mediator complex subunit 17	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322411	Ell	elongation factor RNA polymerase II	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118326
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20181227	MGI			
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991918
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991918
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201231	MGI			
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20260402	MGI			
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19332510
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19332510
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20201022	MGI			
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991918
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:19332510
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991918
1322414	Slc47a1	solute carrier family 47, member 1	gene	MP:0009641	kidney degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991918
1322419	Ttc39a	tetratricopeptide repeat domain 39A	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1322419	Ttc39a	tetratricopeptide repeat domain 39A	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1322419	Ttc39a	tetratricopeptide repeat domain 39A	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20181227	MGI			
1322419	Ttc39a	tetratricopeptide repeat domain 39A	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12122115
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141009	MGI			PMID:24736975
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:17382312
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765423
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765423
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141009	MGI			PMID:24736975
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141009	MGI			PMID:24736975
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0002905	decreased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141009	MGI			PMID:24736975
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0003433	decreased activity of parathyroid		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0003494	parathyroid hypoplasia		IAGP		N	RGD:5509061	20141009	MGI			PMID:24736975
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0006339	abnormal third pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17382312
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765423
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765423
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141009	MGI			PMID:24736975
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10910362
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765423
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765423
1322421	Gcm2	glial cells missing homolog 2	gene	MP:0013573	abnormal parathyroid gland development		IAGP		N	RGD:5509061	20150305	MGI			PMID:17382312
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23663453
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538915
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20221215	MGI			
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23663453
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20181227	MGI			
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210128	MGI			
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0004831	long incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23663453
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23663453
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23663453
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538915
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23663453
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23663453
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998389
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0008758	abnormal T cell receptor beta chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0009263	abnormal eyelid fusion		IEA		N	RGD:5509061	20210520	MGI			
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0010864	abnormal enamel knot morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092943
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23663453
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0013741	absent thymus corticomedullary boundary		IAGP		N	RGD:5509061	20150430	MGI			PMID:12717433
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0030079	small incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0030420	short basicranium		IAGP		N	RGD:5509061	20171214	MGI			PMID:23727454
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0030453	abnormal odontoblast morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0030471	abnormal ameloblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0030518	abnormal outer dental epithelium morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0030522	abnormal stellate reticulum morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0030526	abnormal enamel cord morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:19251658
1322423	Bcl11b	B cell leukemia/lymphoma 11B	gene	MP:0030605	abnormal corneocyte morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:19092943
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:18922680
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0000578	ulcerated autopod		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20180830	MGI			PMID:18922680
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20180830	MGI			PMID:18922680
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20240829	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240829	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0002606	increased basophil cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0005275	abnormal skin tensile strength		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20180830	MGI			PMID:18922680
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20210128	MGI			
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0009827	skin detachment		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0011159	abnormal epidermal-dermal junction morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17322897
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20160929	MGI			PMID:25310407
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0011871	podocyte hypertrophy		IAGP		N	RGD:5509061	20150430	MGI			PMID:22457199
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0012400	nail dystrophy		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0012402	abnormal nail bed morphology		IAGP		N	RGD:5509061	20240822	MGI			PMID:37796769
1322426	Col17a1	collagen, type XVII, alpha 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1322428	Cdc42ep1	CDC42 effector protein 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20221201	MGI			PMID:24451259
1322428	Cdc42ep1	CDC42 effector protein 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:24451259
1322428	Cdc42ep1	CDC42 effector protein 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20221201	MGI			PMID:24451259
1322428	Cdc42ep1	CDC42 effector protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20221201	MGI			PMID:24451259
1322428	Cdc42ep1	CDC42 effector protein 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:24451259
1322428	Cdc42ep1	CDC42 effector protein 1	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:24451259
1322428	Cdc42ep1	CDC42 effector protein 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20221201	MGI			PMID:24451259
1322428	Cdc42ep1	CDC42 effector protein 1	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20221201	MGI			PMID:24451259
1322428	Cdc42ep1	CDC42 effector protein 1	gene	MP:0020329	decreased capillary density		IAGP		N	RGD:5509061	20221201	MGI			PMID:24451259
1322429	Exoc3l	exocyst complex component 3-like	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1322429	Exoc3l	exocyst complex component 3-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240328	MGI			PMID:37661429
1322429	Exoc3l	exocyst complex component 3-like	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220519	MGI			
1322431	Ipo11	importin 11	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1322431	Ipo11	importin 11	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1322431	Ipo11	importin 11	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191205	MGI			
1322431	Ipo11	importin 11	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1322431	Ipo11	importin 11	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1322431	Ipo11	importin 11	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1322431	Ipo11	importin 11	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1322431	Ipo11	importin 11	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1322431	Ipo11	importin 11	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1322431	Ipo11	importin 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322431	Ipo11	importin 11	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1322431	Ipo11	importin 11	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1322431	Ipo11	importin 11	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1322431	Ipo11	importin 11	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1322433	Neb	nebulin	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23715096
1322433	Neb	nebulin	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769824
1322433	Neb	nebulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769824
1322433	Neb	nebulin	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23715096
1322433	Neb	nebulin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23715096
1322433	Neb	nebulin	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23715096
1322433	Neb	nebulin	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769824
1322433	Neb	nebulin	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769824
1322433	Neb	nebulin	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769824
1322433	Neb	nebulin	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23715096
1322433	Neb	nebulin	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20170314	MGI			PMID:24046450
1322433	Neb	nebulin	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20170314	MGI			PMID:24046450
1322433	Neb	nebulin	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0009398	abnormal skeletal muscle fiber size		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23715096
1322433	Neb	nebulin	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0009405	increased skeletal muscle fiber number		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769824
1322433	Neb	nebulin	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16769824
1322433	Neb	nebulin	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23715096
1322433	Neb	nebulin	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200430	MGI			PMID:32066503
1322433	Neb	nebulin	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20170427	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0014921	decreased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:23715096
1322433	Neb	nebulin	gene	MP:0014921	decreased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0030566	abnormal A band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:16769824
1322433	Neb	nebulin	gene	MP:0030566	abnormal A band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26123491
1322433	Neb	nebulin	gene	MP:0030567	abnormal I band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:16769824
1322433	Neb	nebulin	gene	MP:0030568	abnormal H zone morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:16902413
1322433	Neb	nebulin	gene	MP:0030568	abnormal H zone morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:26123491
1322434	Aasdh	aminoadipate-semialdehyde dehydrogenase	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1322434	Aasdh	aminoadipate-semialdehyde dehydrogenase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1322434	Aasdh	aminoadipate-semialdehyde dehydrogenase	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20221215	MGI			
1322436	Tmem259	transmembrane protein 259	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1322441	Aire	autoimmune regulator	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015306
1322441	Aire	autoimmune regulator	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696775
1322441	Aire	autoimmune regulator	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1322441	Aire	autoimmune regulator	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696775
1322441	Aire	autoimmune regulator	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696775
1322441	Aire	autoimmune regulator	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265170
1322441	Aire	autoimmune regulator	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015306
1322441	Aire	autoimmune regulator	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854172
1322441	Aire	autoimmune regulator	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0001868	ovary inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141211	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20230622	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360567
1322441	Aire	autoimmune regulator	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854172
1322441	Aire	autoimmune regulator	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265170
1322441	Aire	autoimmune regulator	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854172
1322441	Aire	autoimmune regulator	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20170105	MGI			
1322441	Aire	autoimmune regulator	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20404099
1322441	Aire	autoimmune regulator	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376594
1322441	Aire	autoimmune regulator	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265170
1322441	Aire	autoimmune regulator	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0003341	chronic pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0003504	thyroid gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0003504	thyroid gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0003608	prostate gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854172
1322441	Aire	autoimmune regulator	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854172
1322441	Aire	autoimmune regulator	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360567
1322441	Aire	autoimmune regulator	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265170
1322441	Aire	autoimmune regulator	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015306
1322441	Aire	autoimmune regulator	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300913
1322441	Aire	autoimmune regulator	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376594
1322441	Aire	autoimmune regulator	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172259
1322441	Aire	autoimmune regulator	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20201022	MGI			
1322441	Aire	autoimmune regulator	gene	MP:0005313	absent adrenal gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854172
1322441	Aire	autoimmune regulator	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854172
1322441	Aire	autoimmune regulator	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376594
1322441	Aire	autoimmune regulator	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0005398	decreased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0005515	uveitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0005515	uveitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265170
1322441	Aire	autoimmune regulator	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696775
1322441	Aire	autoimmune regulator	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0006194	keratoconjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696775
1322441	Aire	autoimmune regulator	gene	MP:0006201	vitreous body inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265170
1322441	Aire	autoimmune regulator	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11854172
1322441	Aire	autoimmune regulator	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300913
1322441	Aire	autoimmune regulator	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300913
1322441	Aire	autoimmune regulator	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709926
1322441	Aire	autoimmune regulator	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0008690	increased interleukin-23 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22490868
1322441	Aire	autoimmune regulator	gene	MP:0008879	submandibular gland inflammation		IAGP		N	RGD:5509061	20141211	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414681
1322441	Aire	autoimmune regulator	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20696775
1322441	Aire	autoimmune regulator	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141204	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20201022	MGI			
1322441	Aire	autoimmune regulator	gene	MP:0009540	absent Hassall's corpuscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015306
1322441	Aire	autoimmune regulator	gene	MP:0010222	abnormal T-helper 17 cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21182094
1322441	Aire	autoimmune regulator	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0012164	abnormal conjunctiva goblet cell morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:20696775
1322441	Aire	autoimmune regulator	gene	MP:0013367	parotid gland inflammation		IAGP		N	RGD:5509061	20141218	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0013367	parotid gland inflammation		IAGP		N	RGD:5509061	20141218	MGI			PMID:19265170
1322441	Aire	autoimmune regulator	gene	MP:0013533	sublingual gland inflammation		IAGP		N	RGD:5509061	20150219	MGI			PMID:19265170
1322441	Aire	autoimmune regulator	gene	MP:0013754	abnormal ocular surface morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:20696775
1322441	Aire	autoimmune regulator	gene	MP:0020220	decreased tear production		IAGP		N	RGD:5509061	20141211	MGI			PMID:15699112
1322441	Aire	autoimmune regulator	gene	MP:0031226	increased CXCL10 level		IAGP		N	RGD:5509061	20210218	MGI			PMID:22490868
1322444	Angptl6	angiopoietin-like 6	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322444	Angptl6	angiopoietin-like 6	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778720
1322445	Garin5a	golgi associated RAB2 interactor 5A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20240801	MGI			PMID:38935810
1322445	Garin5a	golgi associated RAB2 interactor 5A	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20240801	MGI			PMID:38935810
1322445	Garin5a	golgi associated RAB2 interactor 5A	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38935810
1322445	Garin5a	golgi associated RAB2 interactor 5A	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20240801	MGI			PMID:38935810
1322447	Dsg2	desmoglein 2	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12494996
1322447	Dsg2	desmoglein 2	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:30115995
1322447	Dsg2	desmoglein 2	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20190502	MGI			
1322447	Dsg2	desmoglein 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20210128	MGI			
1322447	Dsg2	desmoglein 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1322447	Dsg2	desmoglein 2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1322447	Dsg2	desmoglein 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1322447	Dsg2	desmoglein 2	gene	MP:0003822	decreased left ventricle systolic pressure		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0003898	abnormal QRS complex		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1322447	Dsg2	desmoglein 2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1322447	Dsg2	desmoglein 2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1322447	Dsg2	desmoglein 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210429	MGI			PMID:30115995
1322447	Dsg2	desmoglein 2	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0010394	decreased QRS amplitude		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0010509	decreased P wave amplitude		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0010631	increased Q wave amplitude		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0010759	decreased right ventricle systolic pressure		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12494996
1322447	Dsg2	desmoglein 2	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12494996
1322447	Dsg2	desmoglein 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1322447	Dsg2	desmoglein 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12494996
1322447	Dsg2	desmoglein 2	gene	MP:0011920	abnormal S wave		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20210204	MGI			PMID:27170944
1322447	Dsg2	desmoglein 2	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20210429	MGI			PMID:30115995
1322447	Dsg2	desmoglein 2	gene	MP:0030578	decreased keratinocyte adhesion		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0031533	abnormal heart left ventricle wall morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0031534	abnormal heart right ventricle wall morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:36268721
1322447	Dsg2	desmoglein 2	gene	MP:0031709	ventricular arrhythmia		IAGP		N	RGD:5509061	20260514	MGI			PMID:36268721
1322451	Mdp1	magnesium-dependent phosphatase 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20170105	MGI			
1322453	Cpne1	copine I	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20241121	MGI			
1322453	Cpne1	copine I	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20241121	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20160421	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210826	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20250227	MGI			PMID:39496954
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20160421	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20201022	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20220519	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20170105	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0008062	abnormal podocyte slit junction morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20250227	MGI			PMID:39496954
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20250227	MGI			PMID:39496954
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20250227	MGI			PMID:39496954
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0013139	moribund		IAGP		N	RGD:5509061	20201015	MGI			PMID:30737270
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1322455	Coq6	coenzyme Q6 monooxygenase	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:39496954
1322458	Ccnt1	cyclin T1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1322458	Ccnt1	cyclin T1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1322458	Ccnt1	cyclin T1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1322458	Ccnt1	cyclin T1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1322458	Ccnt1	cyclin T1	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20230622	MGI			PMID:17938200
1322458	Ccnt1	cyclin T1	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20230622	MGI			PMID:17938200
1322458	Ccnt1	cyclin T1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1322458	Ccnt1	cyclin T1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1322458	Ccnt1	cyclin T1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1322458	Ccnt1	cyclin T1	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20230622	MGI			PMID:17938200
1322458	Ccnt1	cyclin T1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1322458	Ccnt1	cyclin T1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1322458	Ccnt1	cyclin T1	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20230622	MGI			PMID:17938200
1322462	Il33	interleukin 33	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20230601	MGI			
1322462	Il33	interleukin 33	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20190418	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:25617473
1322462	Il33	interleukin 33	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20160922	MGI			PMID:25617473
1322462	Il33	interleukin 33	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:25617473
1322462	Il33	interleukin 33	gene	MP:0001819	abnormal immune cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23248269
1322462	Il33	interleukin 33	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1322462	Il33	interleukin 33	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1322462	Il33	interleukin 33	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20211202	MGI			PMID:32240120
1322462	Il33	interleukin 33	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20190418	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1322462	Il33	interleukin 33	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22331917
1322462	Il33	interleukin 33	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20190418	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20160922	MGI			PMID:25617473
1322462	Il33	interleukin 33	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20160922	MGI			PMID:25617473
1322462	Il33	interleukin 33	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20160922	MGI			PMID:25617473
1322462	Il33	interleukin 33	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20190418	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20190418	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22331917
1322462	Il33	interleukin 33	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23248269
1322462	Il33	interleukin 33	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22331917
1322462	Il33	interleukin 33	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23248269
1322462	Il33	interleukin 33	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1322462	Il33	interleukin 33	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22331917
1322462	Il33	interleukin 33	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20160922	MGI			PMID:25617473
1322462	Il33	interleukin 33	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20190418	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1322462	Il33	interleukin 33	gene	MP:0008655	decreased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1322462	Il33	interleukin 33	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1322462	Il33	interleukin 33	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1322462	Il33	interleukin 33	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1322462	Il33	interleukin 33	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20160922	MGI			PMID:25617473
1322462	Il33	interleukin 33	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937871
1322462	Il33	interleukin 33	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1322462	Il33	interleukin 33	gene	MP:0010862	decreased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22331917
1322462	Il33	interleukin 33	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20190418	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:28675392
1322462	Il33	interleukin 33	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:25617473
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0003695	delayed blastocyst hatching from the zona pellucida		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0012129	failure of blastocyst formation		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322468	Brf1	BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1322470	Alox12	arachidonate 12-lipoxygenase	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:10383730
1322470	Alox12	arachidonate 12-lipoxygenase	gene	MP:0009586	increased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501222
1322470	Alox12	arachidonate 12-lipoxygenase	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:9501222
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0002959	increased urine microalbumin level		IEA		N	RGD:5509061	20181227	MGI			
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0003708	binucleate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20151224	MGI			PMID:26642356
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322472	Nek7	NIMA (never in mitosis gene a)-related expressed kinase 7	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20473324
1322473	Ufsp2	UFM1-specific peptidase 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1322473	Ufsp2	UFM1-specific peptidase 2	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1322473	Ufsp2	UFM1-specific peptidase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322473	Ufsp2	UFM1-specific peptidase 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1322473	Ufsp2	UFM1-specific peptidase 2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1322475	Fam20b	FAM20B, glycosaminoglycan xylosylkinase	gene	MP:0000597	delayed hepatic development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1322475	Fam20b	FAM20B, glycosaminoglycan xylosylkinase	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1322475	Fam20b	FAM20B, glycosaminoglycan xylosylkinase	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1322475	Fam20b	FAM20B, glycosaminoglycan xylosylkinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1322475	Fam20b	FAM20B, glycosaminoglycan xylosylkinase	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1322475	Fam20b	FAM20B, glycosaminoglycan xylosylkinase	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1322475	Fam20b	FAM20B, glycosaminoglycan xylosylkinase	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1322475	Fam20b	FAM20B, glycosaminoglycan xylosylkinase	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1322475	Fam20b	FAM20B, glycosaminoglycan xylosylkinase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20230810	MGI			PMID:21262768
1322477	Cdc14b	CDC14 cell division cycle 14B	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:21262768
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0000161	scoliosis		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0000445	short snout		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0000629	absent mammary gland		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0003451	absent olfactory bulb		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0004163	abnormal adenohypophysis morphology		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0005157	holoprosencephaly		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0008128	abnormal brain internal capsule morphology		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0010589	common truncal valve		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0013186	abnormal basilar artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0013952	retroesophageal left subclavian artery		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0013977	symmetric azygos veins		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0013981	double lumen aortic arch		IEA		N	RGD:5509061	20170504	MGI			
1322481	Dhx35	DEAH-box helicase 35	gene	MP:0013996	abnormal vertebral artery origin		IEA		N	RGD:5509061	20170504	MGI			
1322485	Gemin6	gem nuclear organelle associated protein 6	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1322485	Gemin6	gem nuclear organelle associated protein 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1322489	Pate4	prostate and testis expressed 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1322489	Pate4	prostate and testis expressed 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20190926	MGI			PMID:30452524
1322489	Pate4	prostate and testis expressed 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20190926	MGI			PMID:30452524
1322489	Pate4	prostate and testis expressed 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20161117	MGI			PMID:26731031
1322489	Pate4	prostate and testis expressed 4	gene	MP:0002673	abnormal sperm number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30452524
1322489	Pate4	prostate and testis expressed 4	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1322489	Pate4	prostate and testis expressed 4	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1322489	Pate4	prostate and testis expressed 4	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1322489	Pate4	prostate and testis expressed 4	gene	MP:0030982	abnormal copulatory plug deposition		IAGP		N	RGD:5509061	20191017	MGI			PMID:30452524
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932191
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:23413832
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000508	right-sided isomerism		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000650	mesocardia		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141120	MGI			PMID:23413832
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000923	abnormal roof plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:23413832
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:23413832
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11699604
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0002224	abnormal spleen size		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932191
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555929
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141120	MGI			PMID:23413832
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0003895	increased ectoderm apoptosis		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004387	abnormal prechordal plate morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004639	fused metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0006061	right atrial isomerism		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20170314	MGI			PMID:18617531
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:23413832
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11699604
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20170314	MGI			PMID:27466203
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20190808	MGI			PMID:22355535
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0009843	decreased neural crest cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141120	MGI			PMID:23413832
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141120	MGI			PMID:23413832
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20170314	MGI			PMID:27466203
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0012709	delayed caudal neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0012793	decreased rhombomere 3 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0012801	decreased rhombomere 5 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651926
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0013001	abnormal enteric neural crest cell morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:23413832
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0013973	abnormal hepatic vein connection		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0014277	alobar holoprosencephaly		IAGP		N	RGD:5509061	20230810	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0014320	abnormal autopod rotation		IAGP		N	RGD:5509061	20240404	MGI			PMID:10677508
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0014804	ventricular situs inversus		IAGP		N	RGD:5509061	20251120	MGI			PMID:29992973
1322492	Zic2	zinc finger protein of the cerebellum 2	gene	MP:0020494	left sided inferior vena cava		IAGP		N	RGD:5509061	20191128	MGI			PMID:29992973
1322499	Tbata	thymus, brain and testes associated	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1322499	Tbata	thymus, brain and testes associated	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1322499	Tbata	thymus, brain and testes associated	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1322499	Tbata	thymus, brain and testes associated	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1322499	Tbata	thymus, brain and testes associated	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1322499	Tbata	thymus, brain and testes associated	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1322499	Tbata	thymus, brain and testes associated	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1322499	Tbata	thymus, brain and testes associated	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20937703
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975937
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364326
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808626
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975937
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364326
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808626
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000829	dilated fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808626
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000924	absent roof plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10693795
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10693795
1322501	Gdf7	growth differentiation factor 7	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975937
1322501	Gdf7	growth differentiation factor 7	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11356025
1322501	Gdf7	growth differentiation factor 7	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11356025
1322501	Gdf7	growth differentiation factor 7	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808626
1322501	Gdf7	growth differentiation factor 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11356025
1322501	Gdf7	growth differentiation factor 7	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11356025
1322501	Gdf7	growth differentiation factor 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11356025
1322501	Gdf7	growth differentiation factor 7	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10693795
1322501	Gdf7	growth differentiation factor 7	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364326
1322501	Gdf7	growth differentiation factor 7	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15975937
1322501	Gdf7	growth differentiation factor 7	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10693795
1322501	Gdf7	growth differentiation factor 7	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10693795
1322501	Gdf7	growth differentiation factor 7	gene	MP:0013318	abnormal branching involved in seminal vesicle morphogenesis		IAGP		N	RGD:5509061	20141204	MGI			PMID:11356025
1322501	Gdf7	growth differentiation factor 7	gene	MP:0013899	abnormal seminal vesicle epithelium morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:11356025
1322501	Gdf7	growth differentiation factor 7	gene	MP:0021091	abnormal dorsal interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:10693795
1322501	Gdf7	growth differentiation factor 7	gene	MP:0021092	abnormal dorsal interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:9808626
1322507	Sephs1	selenophosphate synthetase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180809	MGI			PMID:27208177
1322507	Sephs1	selenophosphate synthetase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180809	MGI			PMID:27208177
1322507	Sephs1	selenophosphate synthetase 1	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:27208177
1322507	Sephs1	selenophosphate synthetase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180809	MGI			PMID:27208177
1322507	Sephs1	selenophosphate synthetase 1	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20180809	MGI			PMID:27208177
1322507	Sephs1	selenophosphate synthetase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180809	MGI			PMID:27208177
1322507	Sephs1	selenophosphate synthetase 1	gene	MP:0030599	decreased liver manganese level		IAGP		N	RGD:5509061	20180809	MGI			PMID:27208177
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220519	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220519	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201022	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20201105	MGI			PMID:32915983
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:32915983
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20210513	MGI			PMID:31495077
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210513	MGI			PMID:31495077
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20200514	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20201105	MGI			PMID:32915983
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20220519	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210520	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:32915983
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0003381	vitreal fibroplasia		IAGP		N	RGD:5509061	20220331	MGI			PMID:32915983
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20200514	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0010255	cortical cataract		IAGP		N	RGD:5509061	20201105	MGI			PMID:32915983
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20210513	MGI			PMID:31495077
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0013732	mature cataract		IAGP		N	RGD:5509061	20201105	MGI			PMID:32915983
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:32915983
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0030949	abnormal Golgi vesicle transport		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0030952	abnormal Golgi stack morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322508	Vps13b	vacuolar protein sorting 13B	gene	MP:0030980	abnormal acroplaxome morphology		IAGP		N	RGD:5509061	20201105	MGI			PMID:31218450
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000079	abnormal basioccipital bone morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000141	abnormal vertebral body morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000297	abnormal atrioventricular cushion morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000445	short snout		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000600	liver hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000632	abnormal pineal gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0000963	fused dorsal root ganglion		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0001879	abnormal lymphatic vessel morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160310	MGI			PMID:25259869
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002108	abnormal muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002191	abnormal artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002237	abnormal nasal cavity morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002239	abnormal nasal septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002243	abnormal vomeronasal organ morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002249	abnormal larynx morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002746	abnormal semilunar valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002951	small thyroid gland		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0003253	dilated bile duct		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0003584	bifid ureter		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0003617	urinary bladder hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0003924	diaphragmatic hernia		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0004110	transposition of great arteries		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0004163	abnormal adenohypophysis morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0004201	fetal growth retardation		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0004666	absent stapedial artery		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20160310	MGI			PMID:25259869
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0005269	abnormal occipital bone morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0006065	abnormal heart position or orientation		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0008386	absent styloid process		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0008534	enlarged fourth ventricle		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0008536	enlarged third ventricle		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0008922	abnormal cervical rib		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0009526	absent sublingual gland		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20170622	MGI			PMID:25259869
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0009570	abnormal right lung morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0009820	abnormal liver vasculature morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20160310	MGI			PMID:25259869
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0009917	abnormal hyoid bone body morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010403	atrial septal defect		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010404	ostium primum atrial septal defect		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010433	double inlet heart left ventricle		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010439	abnormal hepatic vein morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010484	bicuspid aortic valve		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010496	abnormal pectinate muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010527	bicuspid pulmonary valve		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010530	cerebral arteriovenous malformation		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010572	persistent right dorsal aorta		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010595	abnormal aortic valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010728	fusion of atlas and occipital bones		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010853	abnormal lung position or orientation		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0010912	herniated liver		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160310	MGI			PMID:25259869
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160310	MGI			PMID:25259869
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160310	MGI			PMID:25259869
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160310	MGI			PMID:25259869
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0011361	pelvic kidney		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0011493	double ureter		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013186	abnormal basilar artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013818	abnormal oral cavity morphology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013826	absent hypoglossal canal		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013845	abnormal eye muscle topology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013846	retropharyngeal edema		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013847	retropleural edema		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013852	abnormal Mullerian duct topology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013855	absent celiac artery		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013871	abnormal stapedial artery topology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013878	abnormal ductus venosus valve topology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013917	persistent right 6th pharyngeal arch artery		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013923	small prevertebral sympathetic ganglia		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013925	abnormal vascular plexus formation		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013930	abnormal digastric muscle connection		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013931	abnormal olfactory bulb position		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013932	fragmented Meckel's cartilage		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013936	abnormal thymus topology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013949	fusion of axis and occipital bones		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013965	abnormally deep median sulcus of tongue		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013976	abnormal left vena cava superior connection		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013977	symmetric azygos veins		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013982	inverse situs of great intrathoracic arteries		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013996	abnormal vertebral artery origin		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013998	absent canalicular internal carotid artery segment		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0013999	absent parasellar internal carotid artery		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0014011	abnormal ovary tissue architecture		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0014017	abnormal Wolffian duct connection		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0014019	embryo cyst		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0020301	short tongue		IEA		N	RGD:5509061	20170504	MGI			
1322511	Sh3pxd2a	SH3 and PX domains 2A	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20210722	MGI			PMID:32991838
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20170209	MGI			PMID:23236180
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000158	absent sternum		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20170209	MGI			PMID:16207837
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20170209	MGI			PMID:23907671
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:19261698
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000282	abnormal interatrial septum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:32991838
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000561	adactyly		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20215352
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15691760
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20170209	MGI			PMID:23907671
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170209	MGI			PMID:15132997
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20170209	MGI			PMID:23907671
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19261698
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210722	MGI			PMID:32991838
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20170209	MGI			PMID:11857796
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20170209	MGI			PMID:15132997
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170209	MGI			PMID:19384968
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170209	MGI			PMID:20806356
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002256	abnormal laryngeal cartilage morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20170209	MGI			PMID:22421045
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002711	decreased glucagon secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:18723011
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:16207837
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20240104	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002785	absent Leydig cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002785	absent Leydig cells		IAGP		N	RGD:5509061	20170209	MGI			PMID:16207837
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002894	abnormal otolith morphology		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20170209	MGI			PMID:11857796
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002898	absent cartilage		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20170209	MGI			PMID:16207837
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:18723011
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20215352
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003153	early eyelid opening		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003416	premature bone ossification		IAGP		N	RGD:5509061	20170209	MGI			PMID:23907671
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003417	premature endochondral bone ossification		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003589	abnormal ureter physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20170209	MGI			PMID:16207837
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:23907671
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:23907671
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20170209	MGI			PMID:18723011
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004318	absent incus		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004319	absent malleus		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004344	scapular bone hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:11857796
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004344	scapular bone hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004344	scapular bone hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004344	scapular bone hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:23907671
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20170209	MGI			PMID:11857796
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004372	bowed fibula		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004493	dilated cochlea		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004506	abnormal pubis morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004507	abnormal ischium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20170209	MGI			PMID:23236180
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004692	small pubis		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20170209	MGI			PMID:20215352
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004862	small scala tympani		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0004880	lung cyst		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11857796
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005354	abnormal ilium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005356	positive geotaxis		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:18723011
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20215352
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20215352
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0005652	sex reversal		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:19261698
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006121	calcified mitral valve		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006328	nonsyndromic hearing impairment		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22421045
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0006424	absent testis cords		IAGP		N	RGD:5509061	20170209	MGI			PMID:16207837
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008090	increased T-helper 2 cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20170209	MGI			PMID:22421045
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008309	dilated scala media		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008385	absent basisphenoid bone		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008386	absent styloid process		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20170209	MGI			PMID:18723011
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009139	failure of Mullerian duct regression		IAGP		N	RGD:5509061	20170209	MGI			PMID:16207837
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009181	decreased pancreatic delta cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18723011
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009186	decreased PP cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:18723011
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20170209	MGI			PMID:19201862
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:22421045
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20170209	MGI			PMID:11857796
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009910	bifurcated tongue		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0009915	absent hyoid bone lesser horns		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010116	abnormal primitive urogenital sinus morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:31669249
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010587	conotruncal ridge hypoplasia		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010684	abnormal hair follicle outer root sheath morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010686	abnormal hair follicle matrix region morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:11857796
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:16203988
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:15132997
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230420	MGI			PMID:36343245
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:15056615
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:21484342
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:16207837
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20170209	MGI			PMID:12414734
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:16085486
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011210	abnormal temporomandibular joint morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:19815519
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011426	abnormal ureter smooth muscle morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011480	impaired ureteric peristalsis		IAGP		N	RGD:5509061	20170209	MGI			PMID:20881014
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011648	thick heart valve cusps		IAGP		N	RGD:5509061	20240104	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20170209	MGI			PMID:24191021
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0012243	decreased hepatoblast number		IAGP		N	RGD:5509061	20240502	MGI			PMID:38321001
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0012756	impaired cranial neural crest cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:16207837
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0013013	abnormal trunk neural crest cell morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:15691760
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0013014	increased trunk neural crest cell apoptosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:15691760
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:26234751
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:11371614
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0030162	absent hyoid bone body		IAGP		N	RGD:5509061	20171005	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0030258	small mandibular condyloid process		IAGP		N	RGD:5509061	20171019	MGI			PMID:19815519
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0030259	mandibular condyloid process hypoplasia		IAGP		N	RGD:5509061	20210722	MGI			PMID:32991838
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0030588	decreased pancreatic alpha cell mass		IAGP		N	RGD:5509061	20180614	MGI			PMID:18723011
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0030835	abnormal ankle joint morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:20215352
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0030868	absent thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:12878728
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0031549	abnormal heart valve development		IAGP		N	RGD:5509061	20240104	MGI			PMID:17350610
1322514	Sox9	SRY (sex determining region Y)-box 9	gene	MP:0031550	abnormal atrioventricular valve development		IAGP		N	RGD:5509061	20240104	MGI			PMID:17350610
1322517	Ptx4	pentraxin 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1322517	Ptx4	pentraxin 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1322519	Itga9	integrin alpha 9	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866676
1322519	Itga9	integrin alpha 9	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22772469
1322519	Itga9	integrin alpha 9	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866676
1322519	Itga9	integrin alpha 9	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22772469
1322519	Itga9	integrin alpha 9	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22772469
1322519	Itga9	integrin alpha 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18633440
1322519	Itga9	integrin alpha 9	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866676
1322519	Itga9	integrin alpha 9	gene	MP:0003660	chylothorax		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866676
1322519	Itga9	integrin alpha 9	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18633440
1322519	Itga9	integrin alpha 9	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18633440
1322519	Itga9	integrin alpha 9	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18633440
1322519	Itga9	integrin alpha 9	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866676
1322519	Itga9	integrin alpha 9	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:18633440
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044949
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:6855886
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:6855886
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002212	abnormal secondary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:6855886
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002213	true hermaphroditism		IAGP		N	RGD:5509061	20141003	MGI			PMID:6855886
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:6855886
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002996	ovotestis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0002996	ovotestis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6855886
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044949
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0005652	sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:6855886
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0006418	abnormal testis cord formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0006424	absent testis cords		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044949
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15044949
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16199873
1322521	Map3k4	mitogen-activated protein kinase kinase kinase 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19753101
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20230601	MGI			
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20231123	MGI			PMID:36748836
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20231123	MGI			PMID:36748836
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20231123	MGI			PMID:36748836
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20221215	MGI			
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20220519	MGI			
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20231123	MGI			PMID:36748836
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20170105	MGI			
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20231123	MGI			PMID:36748836
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20231123	MGI			PMID:36748836
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20231123	MGI			PMID:36748836
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20231123	MGI			PMID:36748836
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1322526	Lyplal1	lysophospholipase-like 1	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20231123	MGI			PMID:36748836
1322528	Tdrkh	tudor and KH domain containing protein	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23714778
1322528	Tdrkh	tudor and KH domain containing protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23714778
1322528	Tdrkh	tudor and KH domain containing protein	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23714778
1322528	Tdrkh	tudor and KH domain containing protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23714778
1322528	Tdrkh	tudor and KH domain containing protein	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23714778
1322528	Tdrkh	tudor and KH domain containing protein	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23714778
1322528	Tdrkh	tudor and KH domain containing protein	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23714778
1322528	Tdrkh	tudor and KH domain containing protein	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23714778
1322528	Tdrkh	tudor and KH domain containing protein	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23714778
1322530	Mkrn3	makorin, ring finger protein, 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230601	MGI			PMID:34692086
1322530	Mkrn3	makorin, ring finger protein, 3	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20230601	MGI			PMID:34692086
1322530	Mkrn3	makorin, ring finger protein, 3	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20230601	MGI			PMID:34692086
1322530	Mkrn3	makorin, ring finger protein, 3	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20230601	MGI			PMID:34692086
1322530	Mkrn3	makorin, ring finger protein, 3	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20230601	MGI			PMID:34692086
1322530	Mkrn3	makorin, ring finger protein, 3	gene	MP:0003378	early sexual maturation		IAGP		N	RGD:5509061	20230601	MGI			PMID:34692086
1322530	Mkrn3	makorin, ring finger protein, 3	gene	MP:0008994	early vaginal opening		IAGP		N	RGD:5509061	20230601	MGI			PMID:34692086
1322530	Mkrn3	makorin, ring finger protein, 3	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1322530	Mkrn3	makorin, ring finger protein, 3	gene	MP:0031399	early balanopreputial separation		IAGP		N	RGD:5509061	20230601	MGI			PMID:34692086
1322533	Peli1	pellino 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1322533	Peli1	pellino 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210805	MGI			
1322533	Peli1	pellino 1	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210805	MGI			
1322533	Peli1	pellino 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210805	MGI			
1322533	Peli1	pellino 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1322533	Peli1	pellino 1	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20210805	MGI			
1322533	Peli1	pellino 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210805	MGI			
1322533	Peli1	pellino 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1322533	Peli1	pellino 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734906
1322533	Peli1	pellino 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210805	MGI			
1322533	Peli1	pellino 1	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734906
1322533	Peli1	pellino 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734906
1322533	Peli1	pellino 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734906
1322533	Peli1	pellino 1	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734906
1322533	Peli1	pellino 1	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734906
1322533	Peli1	pellino 1	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322533	Peli1	pellino 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734906
1322533	Peli1	pellino 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734906
1322533	Peli1	pellino 1	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734906
1322533	Peli1	pellino 1	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22902624
1322535	Surf4	surfeit gene 4	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1322535	Surf4	surfeit gene 4	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20211223	MGI			PMID:33186557
1322535	Surf4	surfeit gene 4	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20211223	MGI			PMID:33186557
1322535	Surf4	surfeit gene 4	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1322535	Surf4	surfeit gene 4	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20211223	MGI			PMID:33186557
1322535	Surf4	surfeit gene 4	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20211223	MGI			PMID:33186557
1322535	Surf4	surfeit gene 4	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:31978056
1322535	Surf4	surfeit gene 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1322536	Pabpc6	poly(A) binding protein, cytoplasmic 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240801	MGI			PMID:38281153
1322538	Trim15	tripartite motif-containing 15	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20200514	MGI			
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20200514	MGI			
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322542	Tm7sf2	transmembrane 7 superfamily member 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403717
1322549	Emilin1	elastin microfibril interfacer 1	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701737
1322549	Emilin1	elastin microfibril interfacer 1	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20160414	MGI			PMID:25658937
1322549	Emilin1	elastin microfibril interfacer 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160414	MGI			PMID:25658937
1322549	Emilin1	elastin microfibril interfacer 1	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701737
1322549	Emilin1	elastin microfibril interfacer 1	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701737
1322549	Emilin1	elastin microfibril interfacer 1	gene	MP:0012356	increased prothrombin time		IAGP		N	RGD:5509061	20160414	MGI			PMID:25658937
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335278
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335278
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335278
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335278
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335278
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335278
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335278
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335278
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335278
1322550	Boll	boule homolog, RNA binding protein	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:20335278
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0000676	abnormal body water content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20170309	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220519	MGI			
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220519	MGI			
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20220519	MGI			
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17908936
1322553	Il36rn	interleukin 36 receptor antagonist	gene	MP:0012572	increased susceptibility to chemically induced skin inflammation		IAGP		N	RGD:5509061	20191114	MGI			PMID:29554104
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322556	Smc6	structural maintenance of chromosomes 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151126	MGI			PMID:23518413
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289463
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20111116	MGI			
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001263	weight loss		IEA		N	RGD:5509061	20111116	MGI			
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002252	abnormal oropharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0004605	abnormal vertebral lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0004711	persistence of notochord tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0004874	abnormal timing of postnatal eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0005229	abnormal intervertebral disk development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0006086	decreased body mass index		IEA		N	RGD:5509061	20111116	MGI			
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0009323	abnormal spleen development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0009524	absent submandibular gland		IAGP		N	RGD:5509061	20150226	MGI			PMID:16289463
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0009576	oral atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0009880	decreased mouth size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16289463
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0010335	fused first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0010335	fused first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21549111
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0013541	abnormal submandibular gland development		IAGP		N	RGD:5509061	20150226	MGI			PMID:16289463
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0013790	single external naris		IAGP		N	RGD:5509061	20150611	MGI			PMID:14681194
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0013790	single external naris		IAGP		N	RGD:5509061	20150611	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0014277	alobar holoprosencephaly		IAGP		N	RGD:5509061	20230810	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0021190	decreased bone mineral density of lumbar vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0030268	agnathia		IAGP		N	RGD:5509061	20171214	MGI			PMID:15013800
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0030279	thin neurocranium		IAGP		N	RGD:5509061	20171102	MGI			PMID:12665593
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0030985	decreased circulating osteocalcin level		IAGP		N	RGD:5509061	20201001	MGI			PMID:16934545
1322558	Twsg1	twisted gastrulation BMP signaling modulator 1	gene	MP:0031109	subarachnoid hemorrhage		IAGP		N	RGD:5509061	20200917	MGI			PMID:12665593
1322561	Vcl	vinculin	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331426
1322561	Vcl	vinculin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0004567	decreased myocardial fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331426
1322561	Vcl	vinculin	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0008932	abnormal embryonic tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331426
1322561	Vcl	vinculin	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331426
1322561	Vcl	vinculin	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331426
1322561	Vcl	vinculin	gene	MP:0010559	heart block		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785437
1322561	Vcl	vinculin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20171214	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0012250	absent heart valves		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0012501	abnormal pericardial cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0012677	absent brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0012677	absent brain ventricles		IAGP		N	RGD:5509061	20161103	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0013164	abnormal forelimb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0013166	small forelimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0013227	small brain ventricles		IAGP		N	RGD:5509061	20161103	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:15331426
1322561	Vcl	vinculin	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:9486805
1322561	Vcl	vinculin	gene	MP:0014699	increased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:20644727
1322561	Vcl	vinculin	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:15331426
1322561	Vcl	vinculin	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15331426
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0001588	abnormal hemoglobin		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788586
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788586
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788586
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788586
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788586
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21788586
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0013657	abnormal blood cell morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24421385
1322568	Abcb10	ATP-binding cassette, sub-family B member 10	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:24421385
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0001889	delayed brain development		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0010545	abnormal heart layer morphology		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0012269	nuchal edema		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322574	Cdk13	cyclin dependent kinase 13	gene	MP:0013580	abnormal nasal gland morphology		IAGP		N	RGD:5509061	20200910	MGI			PMID:31440507
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160421	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20160421	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001606	impaired hematopoiesis		IEA		N	RGD:5509061	20161201	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11869686
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649478
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649478
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002145	abnormal T cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14568969
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14568969
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9003785
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14568969
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586083
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0002814	hyperchromasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10221648
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235116
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649478
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9003785
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9862367
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15818410
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235116
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:14568969
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0004978	decreased B-1 B cell number		IEA		N	RGD:5509061	20161201	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586083
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20161201	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9003785
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10221648
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649478
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9862367
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10221648
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235116
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649478
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235116
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14568969
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14568969
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20161201	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20161201	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20161201	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20161201	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12235116
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008093	abnormal memory B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9862367
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008112	abnormal monocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649478
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649478
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649478
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7649478
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11869686
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0010842	decreased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20161201	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0014347	increased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:9529314
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:10518539
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20161201	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20190418	MGI			
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:9862367
1322581	Rel	Rel proto-oncogene, NFKB subunit	gene	MP:0030582	abnormal hair follicle placode formation		IAGP		N	RGD:5509061	20180614	MGI			PMID:15199130
1322584	Bhlha9	basic helix-loop-helix family, member a9	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141127	MGI			PMID:24852374
1322584	Bhlha9	basic helix-loop-helix family, member a9	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141127	MGI			PMID:24852374
1322584	Bhlha9	basic helix-loop-helix family, member a9	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20181227	MGI			
1322584	Bhlha9	basic helix-loop-helix family, member a9	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20181227	MGI			
1322584	Bhlha9	basic helix-loop-helix family, member a9	gene	MP:0009874	abnormal interdigital cell death		IAGP		N	RGD:5509061	20141127	MGI			PMID:24852374
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0004006	impaired contractility of jejunal smooth muscle		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0011503	distended jejunum		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0011881	distended duodenum		IAGP		N	RGD:5509061	20210819	MGI			PMID:33424621
1322586	Myl9	myosin, light polypeptide 9, regulatory	gene	MP:0014605	dark liver		IAGP		N	RGD:5509061	20250206	MGI			PMID:33424621
1322588	Slc39a9	solute carrier family 39 (zinc transporter), member 9	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20260402	MGI			
1322588	Slc39a9	solute carrier family 39 (zinc transporter), member 9	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1322588	Slc39a9	solute carrier family 39 (zinc transporter), member 9	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20260402	MGI			
1322588	Slc39a9	solute carrier family 39 (zinc transporter), member 9	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20260402	MGI			
1322588	Slc39a9	solute carrier family 39 (zinc transporter), member 9	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20260402	MGI			
1322588	Slc39a9	solute carrier family 39 (zinc transporter), member 9	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20260402	MGI			
1322588	Slc39a9	solute carrier family 39 (zinc transporter), member 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1322588	Slc39a9	solute carrier family 39 (zinc transporter), member 9	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20260402	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210128	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20260402	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20260402	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0008913	weaving		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196968
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20220519	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20211021	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20211021	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20210128	MGI			
1322591	Ltn1	listerin E3 ubiquitin protein ligase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1322593	Pdcd6	programmed cell death 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024023
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0000749	muscle degeneration		IEA		N	RGD:5509061	20141003	MGI			
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0003644	thymus atrophy		IEA		N	RGD:5509061	20141003	MGI			
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0004545	enlarged esophagus		IEA		N	RGD:5509061	20141003	MGI			
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0010788	stomach hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0011085	postnatal lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1322597	Dhrs7b	dehydrogenase/reductase 7B	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20241121	MGI			
1322600	Rsf1	remodeling and spacing factor 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1322600	Rsf1	remodeling and spacing factor 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1322600	Rsf1	remodeling and spacing factor 1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20191107	MGI			PMID:30348983
1322600	Rsf1	remodeling and spacing factor 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1322600	Rsf1	remodeling and spacing factor 1	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20191107	MGI			PMID:30348983
1322600	Rsf1	remodeling and spacing factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1322603	Dlgap5	DLG associated protein 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676373
1322603	Dlgap5	DLG associated protein 5	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676373
1322606	Atosb	atos homolog B	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1322606	Atosb	atos homolog B	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20260402	MGI			
1322606	Atosb	atos homolog B	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1322606	Atosb	atos homolog B	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20260402	MGI			
1322606	Atosb	atos homolog B	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1322608	Slc35h1	solute carrier family 35 member H1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20241010	MGI			PMID:38270391
1322608	Slc35h1	solute carrier family 35 member H1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20241010	MGI			PMID:38270391
1322608	Slc35h1	solute carrier family 35 member H1	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20241010	MGI			PMID:38270391
1322608	Slc35h1	solute carrier family 35 member H1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20241010	MGI			PMID:38270391
1322608	Slc35h1	solute carrier family 35 member H1	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20241010	MGI			PMID:38270391
1322608	Slc35h1	solute carrier family 35 member H1	gene	MP:0004648	decreased thoracic vertebrae number		IAGP		N	RGD:5509061	20241010	MGI			PMID:38270391
1322608	Slc35h1	solute carrier family 35 member H1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20241010	MGI			PMID:38270391
1322608	Slc35h1	solute carrier family 35 member H1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20241010	MGI			PMID:38270391
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728642
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12378523
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12378523
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12378523
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728642
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12378523
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728642
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728642
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14707112
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0012072	decreased susceptibility to osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1322611	Hivep3	human immunodeficiency virus type I enhancer binding protein 3	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:23945236
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0003708	binucleate		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0004575	small limb buds		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0009852	increased Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20160728	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:25521379
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220811	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0031352	absent sperm axonemal central pair		IAGP		N	RGD:5509061	20220811	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0031373	abnormal manchette perinuclear ring morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0031375	abnormal manchette disassembly		IAGP		N	RGD:5509061	20220407	MGI			PMID:22654669
1322616	Katnb1	katanin p80 (WD40-containing) subunit B 1	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20220428	MGI			PMID:22654669
1322618	Slx9	SLX9 ribosome biogenesis factor	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230720	MGI			
1322620	Srrm1	serine/arginine repetitive matrix 1	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20250508	MGI			
1322620	Srrm1	serine/arginine repetitive matrix 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20250508	MGI			
1322620	Srrm1	serine/arginine repetitive matrix 1	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20250508	MGI			
1322620	Srrm1	serine/arginine repetitive matrix 1	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20250508	MGI			
1322620	Srrm1	serine/arginine repetitive matrix 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20250508	MGI			
1322620	Srrm1	serine/arginine repetitive matrix 1	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20250508	MGI			
1322620	Srrm1	serine/arginine repetitive matrix 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1322622	Mmgt2	membrane magnesium transporter 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1322622	Mmgt2	membrane magnesium transporter 2	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1322622	Mmgt2	membrane magnesium transporter 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1322622	Mmgt2	membrane magnesium transporter 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1322628	Ltv1	LTV1 ribosome biogenesis factor	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1322628	Ltv1	LTV1 ribosome biogenesis factor	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20240919	MGI			
1322628	Ltv1	LTV1 ribosome biogenesis factor	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1322628	Ltv1	LTV1 ribosome biogenesis factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1322628	Ltv1	LTV1 ribosome biogenesis factor	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20240919	MGI			
1322631	Tex15	testis expressed gene 15 meiosis and synapsis associated	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18283110
1322631	Tex15	testis expressed gene 15 meiosis and synapsis associated	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18283110
1322631	Tex15	testis expressed gene 15 meiosis and synapsis associated	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18283110
1322631	Tex15	testis expressed gene 15 meiosis and synapsis associated	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18283110
1322631	Tex15	testis expressed gene 15 meiosis and synapsis associated	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18283110
1322631	Tex15	testis expressed gene 15 meiosis and synapsis associated	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:18283110
1322639	Ippk	inositol 1,3,4,5,6-pentakisphosphate 2-kinase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221103	MGI			
1322639	Ippk	inositol 1,3,4,5,6-pentakisphosphate 2-kinase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20221103	MGI			
1322639	Ippk	inositol 1,3,4,5,6-pentakisphosphate 2-kinase	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15939868
1322639	Ippk	inositol 1,3,4,5,6-pentakisphosphate 2-kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322639	Ippk	inositol 1,3,4,5,6-pentakisphosphate 2-kinase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20221103	MGI			
1322641	Alg9	ALG9 alpha-1,2-mannosyltransferase	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20241121	MGI			
1322641	Alg9	ALG9 alpha-1,2-mannosyltransferase	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
1322641	Alg9	ALG9 alpha-1,2-mannosyltransferase	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20260402	MGI			
1322641	Alg9	ALG9 alpha-1,2-mannosyltransferase	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1322641	Alg9	ALG9 alpha-1,2-mannosyltransferase	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1322641	Alg9	ALG9 alpha-1,2-mannosyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322641	Alg9	ALG9 alpha-1,2-mannosyltransferase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1322642	Mcrip2	MAPK regulated corepressor interacting protein 2	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20220120	MGI			PMID:34088848
1322642	Mcrip2	MAPK regulated corepressor interacting protein 2	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20220120	MGI			PMID:34088848
1322642	Mcrip2	MAPK regulated corepressor interacting protein 2	gene	MP:0020520	whitened brown adipose tissue morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:34088848
1322646	Foxh1	forkhead box H1	gene	MP:0000024	lowered ear position		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0000087	absent mandible		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0000477	abnormal intestine morphology		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0000508	right-sided isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0000650	mesocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0000690	absent spleen		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0001890	anencephaly		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25511461
1322646	Foxh1	forkhead box H1	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0003104	acrania		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0003388	absent pericardium		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0003872	absent heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0003924	diaphragmatic hernia		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0004113	abnormal aortic arch morphology		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0004733	abnormal thoracic cavity morphology		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0005163	cyclopia		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0006061	right atrial isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363409
1322646	Foxh1	forkhead box H1	gene	MP:0006290	proboscis		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0009880	decreased mouth size		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0010406	common atrium		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0010431	atrial situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0010432	common ventricle		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0010446	heart left ventricle hypoplasia		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0010487	abnormal right subclavian artery morphology		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0010668	abnormal hepatic portal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0011250	abdominal situs ambiguus		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0011253	situs inversus with levocardia		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0011323	abnormal renal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0011569	abnormal azygos vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12642485
1322646	Foxh1	forkhead box H1	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0011668	double outlet right ventricle, Taussig bing type		IEA		N	RGD:5509061	20150226	MGI			
1322646	Foxh1	forkhead box H1	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0012165	absent neural folds		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0012276	absent prechordal mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0012501	abnormal pericardial cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0012739	abnormal anterior primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11358869
1322646	Foxh1	forkhead box H1	gene	MP:0030324	abnormal anterior head development		IAGP		N	RGD:5509061	20180118	MGI			PMID:11358869
1322648	Prss53	serine protease 53	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20200402	MGI			
1322648	Prss53	serine protease 53	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20200402	MGI			
1322648	Prss53	serine protease 53	gene	MP:0002073	abnormal hair growth		IEA		N	RGD:5509061	20201022	MGI			
1322648	Prss53	serine protease 53	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20181227	MGI			
1322648	Prss53	serine protease 53	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1322648	Prss53	serine protease 53	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1322648	Prss53	serine protease 53	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1322648	Prss53	serine protease 53	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20181227	MGI			
1322652	Dnttip1	deoxynucleotidyltransferase, terminal, interacting protein 1	gene	MP:0000215	absent erythrocytes		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1322652	Dnttip1	deoxynucleotidyltransferase, terminal, interacting protein 1	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1322652	Dnttip1	deoxynucleotidyltransferase, terminal, interacting protein 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1322652	Dnttip1	deoxynucleotidyltransferase, terminal, interacting protein 1	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1322652	Dnttip1	deoxynucleotidyltransferase, terminal, interacting protein 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1322652	Dnttip1	deoxynucleotidyltransferase, terminal, interacting protein 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1322652	Dnttip1	deoxynucleotidyltransferase, terminal, interacting protein 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20220811	MGI			
1322652	Dnttip1	deoxynucleotidyltransferase, terminal, interacting protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20201224	MGI			PMID:32591534
1322652	Dnttip1	deoxynucleotidyltransferase, terminal, interacting protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322655	Prss35	serine protease 35	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20231207	MGI			
1322655	Prss35	serine protease 35	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20220811	MGI			
1322655	Prss35	serine protease 35	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1322655	Prss35	serine protease 35	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180705	MGI			PMID:23451081
1322655	Prss35	serine protease 35	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20260402	MGI			
1322655	Prss35	serine protease 35	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210826	MGI			
1322655	Prss35	serine protease 35	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20210826	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230119	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20231207	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230601	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20250508	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1322657	Champ1	chromosome alignment maintaining phosphoprotein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1322659	Ttc5	tetratricopeptide repeat domain 5	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20250508	MGI			
1322664	Cd109	CD109 antigen	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20230601	MGI			
1322664	Cd109	CD109 antigen	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20221215	MGI			
1322664	Cd109	CD109 antigen	gene	MP:0009612	thick epidermis suprabasal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0009715	thick epidermis stratum basale		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0009794	sebaceous gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0010678	abnormal skin adnexa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0010682	abnormal hair follicle infundibulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322664	Cd109	CD109 antigen	gene	MP:0010699	dilated hair follicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22846721
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38767782
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20240808	MGI			PMID:38767782
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20240808	MGI			PMID:38767782
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20240808	MGI			PMID:38767782
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0012006	abnormal hippocampus physiology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0014369	enhanced spatial working memory		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0020870	decreased thigmotaxis		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322666	Dcaf11	DDB1 and CUL4 associated factor 11	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20240808	MGI			PMID:38301772
1322668	Spag9	sperm associated antigen 9	gene	MP:0000371	diluted coat color		IEA		N	RGD:5509061	20111116	MGI			
1322668	Spag9	sperm associated antigen 9	gene	MP:0001189	absent skin pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1322668	Spag9	sperm associated antigen 9	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18574703
1322668	Spag9	sperm associated antigen 9	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18574703
1322668	Spag9	sperm associated antigen 9	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18574703
1322668	Spag9	sperm associated antigen 9	gene	MP:0009280	decreased activated sperm motility		IEA		N	RGD:5509061	20111116	MGI			
1322674	Nlrx1	NLR family member X1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1322674	Nlrx1	NLR family member X1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21703540
1322674	Nlrx1	NLR family member X1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1322674	Nlrx1	NLR family member X1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21703540
1322674	Nlrx1	NLR family member X1	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21703540
1322674	Nlrx1	NLR family member X1	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21703540
1322674	Nlrx1	NLR family member X1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21703540
1322674	Nlrx1	NLR family member X1	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21703540
1322674	Nlrx1	NLR family member X1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21703540
1322674	Nlrx1	NLR family member X1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:21703540
1322674	Nlrx1	NLR family member X1	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:21703540
1322677	Dmap1	DNA methyltransferase 1-associated protein 1	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383065
1322677	Dmap1	DNA methyltransferase 1-associated protein 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383065
1322677	Dmap1	DNA methyltransferase 1-associated protein 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383065
1322677	Dmap1	DNA methyltransferase 1-associated protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322677	Dmap1	DNA methyltransferase 1-associated protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322677	Dmap1	DNA methyltransferase 1-associated protein 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1322679	Camta2	calmodulin binding transcription activator 2	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16678093
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:32658897
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:32658897
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20160630	MGI			PMID:26116663
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0004264	abnormal extraembryonic tissue physiology		IAGP		N	RGD:5509061	20160630	MGI			PMID:26116663
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20160630	MGI			PMID:26116663
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15189737
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160630	MGI			PMID:26116663
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:32658897
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20160630	MGI			PMID:26116663
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20230817	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0031594	increased cardiac jelly amount		IAGP		N	RGD:5509061	20240229	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0031612	increased fetal cardiomyocyte number		IAGP		N	RGD:5509061	20240321	MGI			PMID:37254794
1322685	Chd4	chromodomain helicase DNA binding protein 4	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:37254794
1322686	Ift122	intraflagellar transport 122	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1322686	Ift122	intraflagellar transport 122	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1322686	Ift122	intraflagellar transport 122	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1322686	Ift122	intraflagellar transport 122	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1322686	Ift122	intraflagellar transport 122	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614141
1322686	Ift122	intraflagellar transport 122	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614141
1322686	Ift122	intraflagellar transport 122	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14614141
1322686	Ift122	intraflagellar transport 122	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0010395	abnormal pharyngeal arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1322686	Ift122	intraflagellar transport 122	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0012531	delayed limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0012720	elongated neck		IAGP		N	RGD:5509061	20141003	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:21209331
1322686	Ift122	intraflagellar transport 122	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:19000668
1322686	Ift122	intraflagellar transport 122	gene	MP:0030312	enlarged pharyngeal arch		IAGP		N	RGD:5509061	20171109	MGI			PMID:21209331
1322693	Pxdc1	PX domain containing 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20221215	MGI			
1322695	Fryl	FRY like transcription coactivator	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20181227	MGI			
1322695	Fryl	FRY like transcription coactivator	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322695	Fryl	FRY like transcription coactivator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0002095	abnormal skin pigmentation		IEA		N	RGD:5509061	20160804	MGI			
1322695	Fryl	FRY like transcription coactivator	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322695	Fryl	FRY like transcription coactivator	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1322695	Fryl	FRY like transcription coactivator	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322695	Fryl	FRY like transcription coactivator	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322695	Fryl	FRY like transcription coactivator	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20180531	MGI			PMID:29409347
1322695	Fryl	FRY like transcription coactivator	gene	MP:0013247	placenta necrosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1322695	Fryl	FRY like transcription coactivator	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:29539633
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20190502	MGI			
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1322696	Smdt1	single-pass membrane protein with aspartate rich tail 1	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:32017711
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0004300	abnormal organ of Corti supporting cell morphology		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0011061	abnormal inner hair cell kinocilium morphology		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0011062	abnormal outer hair cell kinocilium morphology		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20220908	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20240405	MGI			PMID:35041619
1322700	Osbpl2	oxysterol binding protein-like 2	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:35041619
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20190502	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20190502	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024029
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024029
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20210520	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024029
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0001725	abnormal umbilical cord morphology		IEA		N	RGD:5509061	20190502	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20190502	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20230601	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20210520	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20190502	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20210128	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12024029
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322702	Mthfd2	methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1322705	Frzb	frizzled-related protein	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491945
1322705	Frzb	frizzled-related protein	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20111116	MGI			
1322705	Frzb	frizzled-related protein	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20111116	MGI			
1322705	Frzb	frizzled-related protein	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1322705	Frzb	frizzled-related protein	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491945
1322705	Frzb	frizzled-related protein	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18050203
1322705	Frzb	frizzled-related protein	gene	MP:0014413	decreased depression-related behavior		IEA		N	RGD:5509061	20240425	MGI			
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20250227	MGI			PMID:34850470
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20250227	MGI			PMID:34850470
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250227	MGI			PMID:34850470
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20171102	MGI			PMID:28867294
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20171102	MGI			PMID:28867294
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20250227	MGI			PMID:34850470
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20250227	MGI			PMID:34850470
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20171102	MGI			PMID:28867294
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20250227	MGI			PMID:34850470
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20250227	MGI			PMID:34850470
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20171102	MGI			PMID:28867294
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20250227	MGI			PMID:34850470
1322712	Ythdf2	YTH N6-methyladenosine RNA binding protein 2	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20250227	MGI			PMID:34850470
1322715	Nckipsd	NCK interacting protein with SH3 domain	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778379
1322715	Nckipsd	NCK interacting protein with SH3 domain	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19302483
1322715	Nckipsd	NCK interacting protein with SH3 domain	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778379
1322715	Nckipsd	NCK interacting protein with SH3 domain	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:19778379
1322715	Nckipsd	NCK interacting protein with SH3 domain	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20190704	MGI			PMID:19302483
1322720	Acyp1	acylphosphatase 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1322720	Acyp1	acylphosphatase 1	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1322722	Nt5c2	5'-nucleotidase, cytosolic II	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20201022	MGI			
1322722	Nt5c2	5'-nucleotidase, cytosolic II	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1322722	Nt5c2	5'-nucleotidase, cytosolic II	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1322722	Nt5c2	5'-nucleotidase, cytosolic II	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191114	MGI			PMID:28325731
1322722	Nt5c2	5'-nucleotidase, cytosolic II	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20180405	MGI			PMID:29342136
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20201231	MGI			
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20200402	MGI			
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0006065	abnormal heart position or orientation		IEA		N	RGD:5509061	20210128	MGI			
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0008172	abnormal follicular B cell morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0008206	increased B-2 B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200213	MGI			PMID:31086255
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160421	MGI			
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20210826	MGI			PMID:30282802
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322724	Otub1	OTU domain, ubiquitin aldehyde binding 1	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20211021	MGI			
1322726	Mcm10	minichromosome maintenance 10 replication initiation factor	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693137
1322726	Mcm10	minichromosome maintenance 10 replication initiation factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693137
1322726	Mcm10	minichromosome maintenance 10 replication initiation factor	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693137
1322726	Mcm10	minichromosome maintenance 10 replication initiation factor	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1322726	Mcm10	minichromosome maintenance 10 replication initiation factor	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693137
1322726	Mcm10	minichromosome maintenance 10 replication initiation factor	gene	MP:0004963	abnormal blastocoele morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693137
1322726	Mcm10	minichromosome maintenance 10 replication initiation factor	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693137
1322726	Mcm10	minichromosome maintenance 10 replication initiation factor	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693137
1322726	Mcm10	minichromosome maintenance 10 replication initiation factor	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:21693137
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240919	MGI			
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38593904
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20240801	MGI			PMID:38593904
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38593904
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20220519	MGI			
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20240606	MGI			PMID:38593904
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322730	Taf5	TATA-box binding protein associated factor 5	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38593904
1322732	Lta4h	leukotriene A4 hydrolase	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20210520	MGI			
1322732	Lta4h	leukotriene A4 hydrolase	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586081
1322732	Lta4h	leukotriene A4 hydrolase	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586081
1322733	Wdr81	WD repeat domain 81	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1322733	Wdr81	WD repeat domain 81	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160609	MGI			PMID:12955145
1322733	Wdr81	WD repeat domain 81	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20190110	MGI			
1322733	Wdr81	WD repeat domain 81	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1322733	Wdr81	WD repeat domain 81	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1322733	Wdr81	WD repeat domain 81	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1322733	Wdr81	WD repeat domain 81	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322733	Wdr81	WD repeat domain 81	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20160630	MGI			PMID:23595742
1322733	Wdr81	WD repeat domain 81	gene	MP:0014345	abnormal neuron mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:23595742
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20150611	MGI			PMID:18343091
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20180607	MGI			PMID:27485015
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000958	peripheral nervous system degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:25116249
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20150611	MGI			PMID:18343091
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160407	MGI			PMID:25116249
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180607	MGI			PMID:27485015
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001506	limp posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20111116	MGI			
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25116249
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0003063	increased coping response		IEA		N	RGD:5509061	20111116	MGI			
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0003225	axonal dystrophy		IEA		N	RGD:5509061	20111116	MGI			
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004143	muscle hypertonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004262	abnormal physical strength		IEA		N	RGD:5509061	20111116	MGI			
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004487	type I spiral ligament fibrocyte degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004489	type III spiral ligament fibrocyte degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20180607	MGI			PMID:27485015
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0008532	decreased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:22423107
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368912
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20150611	MGI			PMID:18343091
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0012712	spinal cord degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14532115
1322735	Slc12a6	solute carrier family 12, member 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22423107
1322737	Rbm28	RNA binding motif protein 28	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1322739	Pigc	phosphatidylinositol glycan anchor biosynthesis, class C	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1322739	Pigc	phosphatidylinositol glycan anchor biosynthesis, class C	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20241121	MGI			
1322739	Pigc	phosphatidylinositol glycan anchor biosynthesis, class C	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1322739	Pigc	phosphatidylinositol glycan anchor biosynthesis, class C	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1322739	Pigc	phosphatidylinositol glycan anchor biosynthesis, class C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322739	Pigc	phosphatidylinositol glycan anchor biosynthesis, class C	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1322743	Kpna3	karyopherin subunit alpha 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151224	MGI			PMID:21479251
1322743	Kpna3	karyopherin subunit alpha 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322743	Kpna3	karyopherin subunit alpha 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322747	Cdc26	cell division cycle 26	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20211021	MGI			
1322747	Cdc26	cell division cycle 26	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322748	4930524B15Rik	RIKEN cDNA 4930524B15 gene	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1322750	Dzank1	double zinc ribbon and ankyrin repeat domains 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20220519	MGI			
1322750	Dzank1	double zinc ribbon and ankyrin repeat domains 1	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1322750	Dzank1	double zinc ribbon and ankyrin repeat domains 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20171116	MGI			PMID:27310661
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20230601	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20230601	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220811	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20220811	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20141003	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230601	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0005262	coloboma		IEA		N	RGD:5509061	20141003	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20230601	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0008926	abnormal anterior definitive endoderm morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0010126	abnormal distal visceral endoderm morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0011255	abnormal anterior visceral endoderm cell migration		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20230601	MGI			
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0012090	midbrain hypoplasia		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322754	Pign	phosphatidylinositol glycan anchor biosynthesis, class N	gene	MP:0030464	abnormal cranial cartilage morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:23213481
1322756	Pipox	pipecolic acid oxidase	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20201022	MGI			
1322756	Pipox	pipecolic acid oxidase	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1322761	Prune2	prune homolog 2	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:29571668
1322765	Trim47	tripartite motif-containing 47	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20260702	MGI			PMID:41667829
1322765	Trim47	tripartite motif-containing 47	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20260702	MGI			PMID:41667829
1322765	Trim47	tripartite motif-containing 47	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20260702	MGI			PMID:41667829
1322765	Trim47	tripartite motif-containing 47	gene	MP:0008431	abnormal short-term spatial reference memory		IAGP		N	RGD:5509061	20260702	MGI			PMID:41667829
1322765	Trim47	tripartite motif-containing 47	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20260702	MGI			PMID:41667829
1322765	Trim47	tripartite motif-containing 47	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20260702	MGI			PMID:41667829
1322765	Trim47	tripartite motif-containing 47	gene	MP:0014600	increased susceptibility to hyperoxia-induced injury		IAGP		N	RGD:5509061	20260702	MGI			PMID:41667829
1322765	Trim47	tripartite motif-containing 47	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220519	MGI			
1322765	Trim47	tripartite motif-containing 47	gene	MP:0031384	impaired blood-brain barrier function		IAGP		N	RGD:5509061	20260702	MGI			PMID:41667829
1322767	Mboat1	membrane bound O-acyltransferase domain containing 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1322767	Mboat1	membrane bound O-acyltransferase domain containing 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210520	MGI			
1322770	Phpt1	phosphohistidine phosphatase 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29440278
1322770	Phpt1	phosphohistidine phosphatase 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29440278
1322770	Phpt1	phosphohistidine phosphatase 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20200409	MGI			PMID:29440278
1322770	Phpt1	phosphohistidine phosphatase 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200409	MGI			PMID:29440278
1322770	Phpt1	phosphohistidine phosphatase 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29440278
1322770	Phpt1	phosphohistidine phosphatase 1	gene	MP:0005573	increased pulmonary respiratory rate		IEA		N	RGD:5509061	20201022	MGI			
1322770	Phpt1	phosphohistidine phosphatase 1	gene	MP:0005574	decreased pulmonary respiratory rate		IEA		N	RGD:5509061	20260402	MGI			
1322770	Phpt1	phosphohistidine phosphatase 1	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1322772	Coq8b	coenzyme Q8B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1322772	Coq8b	coenzyme Q8B	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0002965	increased circulating serum albumin level		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1322772	Coq8b	coenzyme Q8B	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1322772	Coq8b	coenzyme Q8B	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1322772	Coq8b	coenzyme Q8B	gene	MP:0008062	abnormal podocyte slit junction morphology		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1322772	Coq8b	coenzyme Q8B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322772	Coq8b	coenzyme Q8B	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20201002	MGI			PMID:32381600
1322772	Coq8b	coenzyme Q8B	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1322772	Coq8b	coenzyme Q8B	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322772	Coq8b	coenzyme Q8B	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1322777	Slc35a1	solute carrier family 35 (CMP-sialic acid transporter), member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1322782	Ptpn3	protein tyrosine phosphatase, non-receptor type 3	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17921143
1322782	Ptpn3	protein tyrosine phosphatase, non-receptor type 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339465
1322782	Ptpn3	protein tyrosine phosphatase, non-receptor type 3	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17921143
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20141003	MGI			
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20160804	MGI			
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0003442	decreased circulating glycerol level		IEA		N	RGD:5509061	20141003	MGI			
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0006206	embryonic lethality between somite formation and embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794329
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507402
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0012183	decreased paraxial mesoderm size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1322787	Epb41l5	erythrocyte membrane protein band 4.1 like 5	gene	MP:0012272	decreased axial mesoderm size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1322791	Tcea3	transcription elongation factor A (SII), 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:22491241
1322793	Eif4g3	eukaryotic translation initiation factor 4 gamma, 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20430745
1322793	Eif4g3	eukaryotic translation initiation factor 4 gamma, 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210520	MGI			PMID:31999954
1322793	Eif4g3	eukaryotic translation initiation factor 4 gamma, 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20430745
1322793	Eif4g3	eukaryotic translation initiation factor 4 gamma, 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20430745
1322793	Eif4g3	eukaryotic translation initiation factor 4 gamma, 3	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20430745
1322793	Eif4g3	eukaryotic translation initiation factor 4 gamma, 3	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20190117	MGI			PMID:29161344
1322793	Eif4g3	eukaryotic translation initiation factor 4 gamma, 3	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:20430745
1322795	Crlf1	cytokine receptor-like factor 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14523086
1322795	Crlf1	cytokine receptor-like factor 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359701
1322795	Crlf1	cytokine receptor-like factor 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359701
1322795	Crlf1	cytokine receptor-like factor 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359701
1322795	Crlf1	cytokine receptor-like factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10359701
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0014396	decreased fat cell mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:30511960
1322797	Pex16	peroxisomal biogenesis factor 16	gene	MP:0020520	whitened brown adipose tissue morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:30511960
1322800	Itgb8	integrin beta 8	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0000264	failure of vascular branching		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16251442
1322800	Itgb8	integrin beta 8	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16251442
1322800	Itgb8	integrin beta 8	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16251442
1322800	Itgb8	integrin beta 8	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16251442
1322800	Itgb8	integrin beta 8	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1322800	Itgb8	integrin beta 8	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20250508	MGI			
1322800	Itgb8	integrin beta 8	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1322800	Itgb8	integrin beta 8	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18343643
1322800	Itgb8	integrin beta 8	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1322800	Itgb8	integrin beta 8	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1322800	Itgb8	integrin beta 8	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16251442
1322800	Itgb8	integrin beta 8	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322800	Itgb8	integrin beta 8	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20200514	MGI			
1322800	Itgb8	integrin beta 8	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18343643
1322800	Itgb8	integrin beta 8	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0012501	abnormal pericardial cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050137
1322800	Itgb8	integrin beta 8	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0004338	small clavicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0004831	long incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17572665
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22581779
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21655088
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322802	Fig4	FIG4 phosphoinositide 5-phosphatase	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23623387
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523579
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523579
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523579
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169894
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523579
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523579
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169894
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523579
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169894
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169894
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523579
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523579
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18523579
1322804	Mmp19	matrix metallopeptidase 19	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169894
1322806	Rpia	ribose 5-phosphate isomerase A	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1322806	Rpia	ribose 5-phosphate isomerase A	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20170105	MGI			
1322806	Rpia	ribose 5-phosphate isomerase A	gene	MP:0003442	decreased circulating glycerol level		IEA		N	RGD:5509061	20201022	MGI			
1322806	Rpia	ribose 5-phosphate isomerase A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20240808	MGI			PMID:39000360
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20240808	MGI			PMID:39000360
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20240808	MGI			PMID:39000360
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20240808	MGI			PMID:39000360
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20240808	MGI			PMID:39000360
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20240808	MGI			PMID:39000360
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20240808	MGI			PMID:39000360
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20240808	MGI			PMID:39000360
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20240808	MGI			PMID:39000360
1322808	Mims2	mitochondrial inner membrane scaffold 2	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:39000360
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20151217	MGI			PMID:24135232
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20151217	MGI			PMID:24135232
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322809	Insc	INSC spindle orientation adaptor protein	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22017987
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25917546
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16859999
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905196
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10915769
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0005158	ovary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150122	MGI			PMID:22922648
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150122	MGI			PMID:22922648
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12913077
1322811	Fanca	Fanconi anemia, complementation group A	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:12913077
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000161	scoliosis		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20220811	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000322	increased granulocyte number		IEA		N	RGD:5509061	20211021	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000458	abnormal mandible morphology		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000552	abnormal radius morphology		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20210128	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20161103	MGI			PMID:22527485
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20220811	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20200514	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20210826	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0002187	abnormal fibula morphology		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20221215	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210826	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20161103	MGI			PMID:22527485
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004507	abnormal ischium morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004689	small ischium		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0005108	abnormal ulna morphology		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20220811	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20220519	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0009455	enhanced cued conditioning behavior		IEA		N	RGD:5509061	20210520	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0009728	abnormal calcaneum morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20210520	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0010870	absent bone trabeculae		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20161110	MGI			PMID:22527485
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20161110	MGI			PMID:26803617
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0013675	decreased Ly6C-positive mature NK cell number		IEA		N	RGD:5509061	20210128	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1322813	Tent5a	terminal nucleotidyltransferase 5A	gene	MP:0030279	thin neurocranium		IAGP		N	RGD:5509061	20171102	MGI			PMID:26803617
1322815	Kirrel3	kirre like nephrin family adhesion molecule 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201022	MGI			PMID:27430022
1322815	Kirrel3	kirre like nephrin family adhesion molecule 3	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637329
1322815	Kirrel3	kirre like nephrin family adhesion molecule 3	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637329
1322815	Kirrel3	kirre like nephrin family adhesion molecule 3	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28815295
1322815	Kirrel3	kirre like nephrin family adhesion molecule 3	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637329
1322815	Kirrel3	kirre like nephrin family adhesion molecule 3	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28815295
1322815	Kirrel3	kirre like nephrin family adhesion molecule 3	gene	MP:0011679	abnormal vomeronasal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637329
1322815	Kirrel3	kirre like nephrin family adhesion molecule 3	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28815295
1322815	Kirrel3	kirre like nephrin family adhesion molecule 3	gene	MP:0020360	abnormal asymmetric synapse morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:28815295
1322821	Foxp4	forkhead box P4	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361625
1322821	Foxp4	forkhead box P4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542185
1322821	Foxp4	forkhead box P4	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542185
1322821	Foxp4	forkhead box P4	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361625
1322821	Foxp4	forkhead box P4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1322821	Foxp4	forkhead box P4	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1322821	Foxp4	forkhead box P4	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542185
1322821	Foxp4	forkhead box P4	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542185
1322821	Foxp4	forkhead box P4	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542185
1322821	Foxp4	forkhead box P4	gene	MP:0003115	abnormal respiratory system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1322821	Foxp4	forkhead box P4	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361625
1322821	Foxp4	forkhead box P4	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361625
1322821	Foxp4	forkhead box P4	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361625
1322821	Foxp4	forkhead box P4	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542185
1322821	Foxp4	forkhead box P4	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1322821	Foxp4	forkhead box P4	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361625
1322821	Foxp4	forkhead box P4	gene	MP:0010949	decreased club cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1322821	Foxp4	forkhead box P4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22675208
1322821	Foxp4	forkhead box P4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15361625
1322821	Foxp4	forkhead box P4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22542185
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0000358	abnormal cell morphology		IEA		N	RGD:5509061	20111222	MGI			
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20111116	MGI			
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20111215	MGI			
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20111116	MGI			
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20111116	MGI			
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0002573	behavioral despair		IEA		N	RGD:5509061	20111116	MGI			
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0004267	abnormal optic tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20111116	MGI			
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20251204	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0006325	impaired hearing		IEA		N	RGD:5509061	20111116	MGI			
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322824	Slc17a5	solute carrier family 17 (anion/sugar transporter), member 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007460
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0002681	increased corpora lutea number		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721306
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721306
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0008870	increased mature ovarian follicle number		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0009012	short diestrus		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0009015	short proestrus		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322826	Abhd2	abhydrolase domain containing 2	gene	MP:0031421	increased superovulation rate		IAGP		N	RGD:5509061	20230119	MGI			PMID:34568325
1322828	Rfxank	regulatory factor X-associated ankyrin-containing protein	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1322828	Rfxank	regulatory factor X-associated ankyrin-containing protein	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1322828	Rfxank	regulatory factor X-associated ankyrin-containing protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1322829	Vps53	VPS53 GARP complex subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18511934
1322829	Vps53	VPS53 GARP complex subunit	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18511934
1322829	Vps53	VPS53 GARP complex subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18511934
1322829	Vps53	VPS53 GARP complex subunit	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20201231	MGI			
1322829	Vps53	VPS53 GARP complex subunit	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18511934
1322829	Vps53	VPS53 GARP complex subunit	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18511934
1322829	Vps53	VPS53 GARP complex subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322832	Lman2l	lectin, mannose-binding 2-like	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20250508	MGI			
1322832	Lman2l	lectin, mannose-binding 2-like	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1322832	Lman2l	lectin, mannose-binding 2-like	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20241121	MGI			
1322832	Lman2l	lectin, mannose-binding 2-like	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1322835	Pgap6	post-glycosylphosphatidylinositol attachment to proteins 6	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1322835	Pgap6	post-glycosylphosphatidylinositol attachment to proteins 6	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1322835	Pgap6	post-glycosylphosphatidylinositol attachment to proteins 6	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20180628	MGI			PMID:27881714
1322835	Pgap6	post-glycosylphosphatidylinositol attachment to proteins 6	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230601	MGI			
1322835	Pgap6	post-glycosylphosphatidylinositol attachment to proteins 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1322835	Pgap6	post-glycosylphosphatidylinositol attachment to proteins 6	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20180628	MGI			PMID:27881714
1322835	Pgap6	post-glycosylphosphatidylinositol attachment to proteins 6	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180628	MGI			PMID:27881714
1322835	Pgap6	post-glycosylphosphatidylinositol attachment to proteins 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1322839	Slc41a1	solute carrier family 41, member 1	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1322839	Slc41a1	solute carrier family 41, member 1	gene	MP:0010093	decreased circulating magnesium level		IAGP		N	RGD:5509061	20240404	MGI			PMID:36049064
1322839	Slc41a1	solute carrier family 41, member 1	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20240314	MGI			PMID:33153064
1322839	Slc41a1	solute carrier family 41, member 1	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20240314	MGI			PMID:33153064
1322841	Il17f	interleukin 17F	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075395
1322841	Il17f	interleukin 17F	gene	MP:0001866	nasal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
1322841	Il17f	interleukin 17F	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119024
1322841	Il17f	interleukin 17F	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
1322841	Il17f	interleukin 17F	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
1322841	Il17f	interleukin 17F	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
1322841	Il17f	interleukin 17F	gene	MP:0002742	enlarged submandibular lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
1322841	Il17f	interleukin 17F	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
1322841	Il17f	interleukin 17F	gene	MP:0003747	mouth mucosal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
1322841	Il17f	interleukin 17F	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
1322841	Il17f	interleukin 17F	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
1322841	Il17f	interleukin 17F	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
1322841	Il17f	interleukin 17F	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
1322841	Il17f	interleukin 17F	gene	MP:0008348	absent gamma-delta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
1322841	Il17f	interleukin 17F	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
1322841	Il17f	interleukin 17F	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
1322841	Il17f	interleukin 17F	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
1322841	Il17f	interleukin 17F	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
1322841	Il17f	interleukin 17F	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19144317
1322841	Il17f	interleukin 17F	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
1322841	Il17f	interleukin 17F	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18411338
1322841	Il17f	interleukin 17F	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19075395
1322841	Il17f	interleukin 17F	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22770884
1322841	Il17f	interleukin 17F	gene	MP:0009787	increased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493731
1322845	Prpf40a	pre-mRNA processing factor 40A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210128	MGI			
1322845	Prpf40a	pre-mRNA processing factor 40A	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1322845	Prpf40a	pre-mRNA processing factor 40A	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1322845	Prpf40a	pre-mRNA processing factor 40A	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1322845	Prpf40a	pre-mRNA processing factor 40A	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1322845	Prpf40a	pre-mRNA processing factor 40A	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1322845	Prpf40a	pre-mRNA processing factor 40A	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1322845	Prpf40a	pre-mRNA processing factor 40A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322845	Prpf40a	pre-mRNA processing factor 40A	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322848	Rrs1	ribosome biogenesis regulator 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1322848	Rrs1	ribosome biogenesis regulator 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322848	Rrs1	ribosome biogenesis regulator 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210520	MGI			
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20240523	MGI			
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20240523	MGI			
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20240523	MGI			
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0004966	abnormal inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17906629
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20240523	MGI			
1322850	Cops8	COP9 signalosome subunit 8	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20240523	MGI			
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615922
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615922
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210520	MGI			
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615922
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615922
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615922
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0008122	decreased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141009	MGI			PMID:24386204
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141009	MGI			PMID:24386204
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0008191	abnormal follicular B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597478
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19615922
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0008550	abnormal circulating interferon-beta level		IAGP		N	RGD:5509061	20141009	MGI			PMID:24386204
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0008573	increased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141009	MGI			PMID:24386204
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141009	MGI			PMID:24386204
1322854	Gpr183	G protein-coupled receptor 183	gene	MP:0014472	impaired B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:19615922
1322856	Gprc5c	G protein-coupled receptor, family C, group 5, member C	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1322856	Gprc5c	G protein-coupled receptor, family C, group 5, member C	gene	MP:0002606	increased basophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1322856	Gprc5c	G protein-coupled receptor, family C, group 5, member C	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1322856	Gprc5c	G protein-coupled receptor, family C, group 5, member C	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1322856	Gprc5c	G protein-coupled receptor, family C, group 5, member C	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1322856	Gprc5c	G protein-coupled receptor, family C, group 5, member C	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840300
1322858	Ppp6r1	protein phosphatase 6, regulatory subunit 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1322858	Ppp6r1	protein phosphatase 6, regulatory subunit 1	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20250508	MGI			
1322858	Ppp6r1	protein phosphatase 6, regulatory subunit 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1322858	Ppp6r1	protein phosphatase 6, regulatory subunit 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1322858	Ppp6r1	protein phosphatase 6, regulatory subunit 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1322861	Ppie	peptidylprolyl isomerase E (cyclophilin E)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1322861	Ppie	peptidylprolyl isomerase E (cyclophilin E)	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20220811	MGI			
1322861	Ppie	peptidylprolyl isomerase E (cyclophilin E)	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1322861	Ppie	peptidylprolyl isomerase E (cyclophilin E)	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1322861	Ppie	peptidylprolyl isomerase E (cyclophilin E)	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220519	MGI			
1322861	Ppie	peptidylprolyl isomerase E (cyclophilin E)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1322861	Ppie	peptidylprolyl isomerase E (cyclophilin E)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1322867	Eef1b2	eukaryotic translation elongation factor 1 beta 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1322867	Eef1b2	eukaryotic translation elongation factor 1 beta 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20240523	MGI			
1322867	Eef1b2	eukaryotic translation elongation factor 1 beta 2	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20210520	MGI			
1322867	Eef1b2	eukaryotic translation elongation factor 1 beta 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1322867	Eef1b2	eukaryotic translation elongation factor 1 beta 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1322867	Eef1b2	eukaryotic translation elongation factor 1 beta 2	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20200402	MGI			
1322867	Eef1b2	eukaryotic translation elongation factor 1 beta 2	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20200402	MGI			
1322867	Eef1b2	eukaryotic translation elongation factor 1 beta 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1322867	Eef1b2	eukaryotic translation elongation factor 1 beta 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:34085701
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:10523500
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20200310	MGI			PMID:28892093
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20250731	MGI			PMID:34085701
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10523500
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:34085701
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20250731	MGI			PMID:34085701
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0008041	absent NK T cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:28892093
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:28892093
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:28892093
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10523500
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382769
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19893033
1322870	Col7a1	collagen, type VII, alpha 1	gene	MP:0030101	carious teeth		IAGP		N	RGD:5509061	20170928	MGI			PMID:19893033
1322874	Dmtn	dematin actin binding protein	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:12011427
1322874	Dmtn	dematin actin binding protein	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12011427
1322874	Dmtn	dematin actin binding protein	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:12011427
1322874	Dmtn	dematin actin binding protein	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12011427
1322874	Dmtn	dematin actin binding protein	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12011427
1322874	Dmtn	dematin actin binding protein	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12011427
1322874	Dmtn	dematin actin binding protein	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:12011427
1322879	Hid1	HID1 domain containing	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1322879	Hid1	HID1 domain containing	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20260402	MGI			
1322879	Hid1	HID1 domain containing	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1322884	Eif2d	eukaryotic translation initiation factor 2D	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1322884	Eif2d	eukaryotic translation initiation factor 2D	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1322884	Eif2d	eukaryotic translation initiation factor 2D	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1322884	Eif2d	eukaryotic translation initiation factor 2D	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20260402	MGI			
1322884	Eif2d	eukaryotic translation initiation factor 2D	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0000023	abnormal ear position		IEA		N	RGD:5509061	20181227	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0003016	increased circulating bicarbonate level		IAGP		N	RGD:5509061	20260702	MGI			PMID:42048445
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20260702	MGI			PMID:42048445
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20161222	MGI			PMID:27824136
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20161222	MGI			PMID:27824136
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20161222	MGI			PMID:27824136
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20181227	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0005634	decreased circulating sodium level		IAGP		N	RGD:5509061	20260702	MGI			PMID:42048445
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0005673	decreased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20161222	MGI			PMID:27824136
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20260702	MGI			PMID:42048445
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20181227	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20190627	MGI			PMID:31097594
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20181227	MGI			
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20161222	MGI			PMID:27824136
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0013305	isosthenuria		IAGP		N	RGD:5509061	20260702	MGI			PMID:42048445
1322887	Lrba	LPS-responsive beige-like anchor	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20161222	MGI			PMID:27824136
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0003908	decreased stereotypic behavior		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0014345	abnormal neuron mitochondrial morphology		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20250410	MGI			PMID:28704368
1322888	Kansl1	KAT8 regulatory NSL complex subunit 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20241107	MGI			PMID:35177641
1322893	Sipa1l3	signal-induced proliferation-associated 1 like 3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20161103	MGI			PMID:26231217
1322893	Sipa1l3	signal-induced proliferation-associated 1 like 3	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:26231217
1322893	Sipa1l3	signal-induced proliferation-associated 1 like 3	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20161103	MGI			PMID:26231217
1322893	Sipa1l3	signal-induced proliferation-associated 1 like 3	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20161103	MGI			PMID:26231217
1322893	Sipa1l3	signal-induced proliferation-associated 1 like 3	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:26231217
1322893	Sipa1l3	signal-induced proliferation-associated 1 like 3	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:26231217
1322893	Sipa1l3	signal-induced proliferation-associated 1 like 3	gene	MP:0011482	posterior iris synechia		IAGP		N	RGD:5509061	20161103	MGI			PMID:26231217
1322897	Ap1ar	adaptor-related protein complex 1 associated regulatory protein	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20190502	MGI			
1322897	Ap1ar	adaptor-related protein complex 1 associated regulatory protein	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1322897	Ap1ar	adaptor-related protein complex 1 associated regulatory protein	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1322897	Ap1ar	adaptor-related protein complex 1 associated regulatory protein	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1322897	Ap1ar	adaptor-related protein complex 1 associated regulatory protein	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1322897	Ap1ar	adaptor-related protein complex 1 associated regulatory protein	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1322897	Ap1ar	adaptor-related protein complex 1 associated regulatory protein	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1322897	Ap1ar	adaptor-related protein complex 1 associated regulatory protein	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20190502	MGI			
1322897	Ap1ar	adaptor-related protein complex 1 associated regulatory protein	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20190502	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20190502	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1322899	Pfdn5	prefoldin 5	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:20956523
1322899	Pfdn5	prefoldin 5	gene	MP:0030966	decreased brain ependyma motile cilium number		IAGP		N	RGD:5509061	20190725	MGI			PMID:20956523
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20240926	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191205	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20191205	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20191205	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20191205	MGI			
1322901	Orc6	origin recognition complex, subunit 6	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322903	Pigh	phosphatidylinositol glycan anchor biosynthesis, class H	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1322903	Pigh	phosphatidylinositol glycan anchor biosynthesis, class H	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20231207	MGI			
1322903	Pigh	phosphatidylinositol glycan anchor biosynthesis, class H	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322903	Pigh	phosphatidylinositol glycan anchor biosynthesis, class H	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1322903	Pigh	phosphatidylinositol glycan anchor biosynthesis, class H	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361974
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361974
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361974
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163358
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543617
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361974
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543617
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543617
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17199045
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0003613	abnormal kidney medulla development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361974
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17199045
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17199045
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163358
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0009573	abnormal right lung middle lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0010816	decreased type I pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361974
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361974
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163358
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543617
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19023080
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011144	thin lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361974
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011144	thin lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011146	abnormal mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361974
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011148	decreased mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367557
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011345	truncated loop of Henle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011438	absent kidney medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011439	abnormal kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322907	Wnt7b	wingless-type MMTV integration site family, member 7B	gene	MP:0011843	abnormal kidney collecting duct epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19060336
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210128	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210128	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0001393	ataxia		IEA		N	RGD:5509061	20141003	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20141003	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20141003	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0002566	abnormal sexual interaction		IEA		N	RGD:5509061	20141003	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201022	MGI			
1322909	Arhgap10	Rho GTPase activating protein 10	gene	MP:0009434	paraparesis		IEA		N	RGD:5509061	20141003	MGI			
1322911	Rras	RAS oncogene related	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1322911	Rras	RAS oncogene related	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1322911	Rras	RAS oncogene related	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20210304	MGI			PMID:22174156
1322911	Rras	RAS oncogene related	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20240523	MGI			
1322911	Rras	RAS oncogene related	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16286923
1322911	Rras	RAS oncogene related	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20210304	MGI			PMID:22174156
1322911	Rras	RAS oncogene related	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16286923
1322911	Rras	RAS oncogene related	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20141003	MGI			
1322911	Rras	RAS oncogene related	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:22174156
1322911	Rras	RAS oncogene related	gene	MP:0006135	artery stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16286923
1322911	Rras	RAS oncogene related	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20141003	MGI			
1322911	Rras	RAS oncogene related	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20141003	MGI			
1322911	Rras	RAS oncogene related	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16286923
1322911	Rras	RAS oncogene related	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230316	MGI			PMID:36719796
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230316	MGI			PMID:36719796
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20230316	MGI			PMID:36719796
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20230316	MGI			PMID:36719796
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20230316	MGI			PMID:36719796
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923475
1322912	Pnpla8	patatin-like phospholipase domain containing 8	gene	MP:0030753	decreased choline level		IAGP		N	RGD:5509061	20230316	MGI			PMID:36719796
1322914	Snorc	secondary ossification center associated regulator of chondrocyte maturation	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20170323	MGI			
1322914	Snorc	secondary ossification center associated regulator of chondrocyte maturation	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20170323	MGI			
1322914	Snorc	secondary ossification center associated regulator of chondrocyte maturation	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20170323	MGI			
1322920	Nmral1	NmrA-like family domain containing 1	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20231207	MGI			
1322920	Nmral1	NmrA-like family domain containing 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1322920	Nmral1	NmrA-like family domain containing 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20201210	MGI			PMID:31796584
1322920	Nmral1	NmrA-like family domain containing 1	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1322920	Nmral1	NmrA-like family domain containing 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20201210	MGI			PMID:31796584
1322920	Nmral1	NmrA-like family domain containing 1	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20201210	MGI			PMID:31796584
1322920	Nmral1	NmrA-like family domain containing 1	gene	MP:0010378	increased respiratory quotient		IEA		N	RGD:5509061	20231207	MGI			
1322920	Nmral1	NmrA-like family domain containing 1	gene	MP:0012125	decreased bronchoconstrictive response		IEA		N	RGD:5509061	20201022	MGI			
1322922	Golm1	golgi membrane protein 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322922	Golm1	golgi membrane protein 1	gene	MP:0011508	abnormal glomerular capillary thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18830387
1322927	Mindy2	MINDY lysine 48 deubiquitinase 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1322927	Mindy2	MINDY lysine 48 deubiquitinase 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20181227	MGI			
1322927	Mindy2	MINDY lysine 48 deubiquitinase 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1322927	Mindy2	MINDY lysine 48 deubiquitinase 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1322927	Mindy2	MINDY lysine 48 deubiquitinase 2	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20181227	MGI			
1322931	Nkd2	naked cuticle 2	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1322931	Nkd2	naked cuticle 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1322931	Nkd2	naked cuticle 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1322931	Nkd2	naked cuticle 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:17438140
1322934	Mmrn2	multimerin 2	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20210603	MGI			PMID:31422156
1322934	Mmrn2	multimerin 2	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:31422156
1322934	Mmrn2	multimerin 2	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20210603	MGI			PMID:31422156
1322939	Lmln	leishmanolysin-like (metallopeptidase M8 family)	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20260402	MGI			
1322939	Lmln	leishmanolysin-like (metallopeptidase M8 family)	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1322942	Myct1	myc target 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1322942	Myct1	myc target 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1322942	Myct1	myc target 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1322942	Myct1	myc target 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1322942	Myct1	myc target 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1322942	Myct1	myc target 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20210520	MGI			PMID:33658356
1322942	Myct1	myc target 1	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20210520	MGI			PMID:33658356
1322942	Myct1	myc target 1	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:33658356
1322942	Myct1	myc target 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1322942	Myct1	myc target 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:33658356
1322942	Myct1	myc target 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1322942	Myct1	myc target 1	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20210520	MGI			PMID:33658356
1322942	Myct1	myc target 1	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20210520	MGI			PMID:33658356
1322942	Myct1	myc target 1	gene	MP:0020202	abnormal macrophage cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:33658356
1322948	Prrx2	paired related homeobox 2	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000448	pointed snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0000486	abnormal pulmonary trunk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1322948	Prrx2	paired related homeobox 2	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0000568	ectopic digits		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1322948	Prrx2	paired related homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1322948	Prrx2	paired related homeobox 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1322948	Prrx2	paired related homeobox 2	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1322948	Prrx2	paired related homeobox 2	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004479	abnormal oval window morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004603	absent vertebral arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004679	xiphoid process foramen		IAGP		N	RGD:5509061	20181018	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004899	absent temporal bone squamous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0004900	absent zygomatic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20181101	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0009744	postaxial polydactyly		IAGP		N	RGD:5509061	20181101	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0009918	abnormal stylohyoid ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0010464	abnormal aortic arch and aortic arch branch attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1322948	Prrx2	paired related homeobox 2	gene	MP:0010564	abnormal fetal ductus arteriosus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1322948	Prrx2	paired related homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0014281	hindlimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0020823	absent pubic symphysis		IAGP		N	RGD:5509061	20181018	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0030297	outer ear hypoplasia		IAGP		N	RGD:5509061	20171102	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0030317	absent maxillary zygomatic process		IAGP		N	RGD:5509061	20171109	MGI			PMID:9729491
1322948	Prrx2	paired related homeobox 2	gene	MP:0030317	absent maxillary zygomatic process		IAGP		N	RGD:5509061	20171109	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0030456	abnormal odontoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0030471	abnormal ameloblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:9876178
1322948	Prrx2	paired related homeobox 2	gene	MP:0030862	absent triquetrum		IAGP		N	RGD:5509061	20181101	MGI			PMID:9882503
1322948	Prrx2	paired related homeobox 2	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:9729491
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890158
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937482
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937482
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937482
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937482
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150596
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937482
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937482
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937482
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937482
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890158
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004300	abnormal organ of Corti supporting cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004375	enlarged frontal bone		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004386	enlarged interparietal bone		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004391	abnormal respiratory conducting tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004430	abnormal Claudius cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004548	dilated esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937482
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004594	abnormal mandibular coronoid process morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004600	abnormal vertebral transverse process morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004670	small vertebral body		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0004840	increased Deiters cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17369402
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150596
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693063
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0010079	increased osteochondroma incidence		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23150596
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17369402
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0011861	increased cranium height		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15809037
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0014277	alobar holoprosencephaly		IAGP		N	RGD:5509061	20230810	MGI			PMID:17156747
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0021170	spinal stenosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0030315	small neurocranium		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0030425	wide intermaxillary suture		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:16890158
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0030536	abnormal diastema morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16890158
1322950	Spry2	sprouty RTK signaling antagonist 2	gene	MP:0031283	increased enchondroma incidence		IAGP		N	RGD:5509061	20220714	MGI			PMID:34423857
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0010580	decreased heart left ventricle size		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28835921
1322952	Ptcd1	pentatricopeptide repeat domain 1	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:28835921
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20190502	MGI			
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20160512	MGI			PMID:25403443
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20160512	MGI			PMID:25403443
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160512	MGI			PMID:25403443
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20190502	MGI			
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25403443
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20160512	MGI			PMID:25403443
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20160512	MGI			PMID:25403443
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1322955	Ccdc88b	coiled-coil domain containing 88B	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20160512	MGI			PMID:25403443
1322958	Sf3a1	splicing factor 3a, subunit 1	gene	MP:0006204	embryonic lethality before implantation		IEA		N	RGD:5509061	20111116	MGI			
1322963	Xcr1	chemokine (C motif) receptor 1	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23670193
1322963	Xcr1	chemokine (C motif) receptor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23670193
1322963	Xcr1	chemokine (C motif) receptor 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19913446
1322963	Xcr1	chemokine (C motif) receptor 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23670193
1322963	Xcr1	chemokine (C motif) receptor 1	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23670193
1322963	Xcr1	chemokine (C motif) receptor 1	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23670193
1322963	Xcr1	chemokine (C motif) receptor 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23670193
1322964	Batf2	basic leucine zipper transcription factor, ATF-like 2	gene	MP:0001393	ataxia		IEA		N	RGD:5509061	20170209	MGI			
1322964	Batf2	basic leucine zipper transcription factor, ATF-like 2	gene	MP:0010750	increased susceptibility to parasitic infection induced morbidity/mortality		IEA		N	RGD:5509061	20141003	MGI			
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20221110	MGI			PMID:33058343
1322967	Kpna4	karyopherin subunit alpha 4	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20210311	MGI			PMID:32320654
1322970	Parvb	parvin, beta	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1322970	Parvb	parvin, beta	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
1322970	Parvb	parvin, beta	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1322970	Parvb	parvin, beta	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1322970	Parvb	parvin, beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18662549
1322970	Parvb	parvin, beta	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1322970	Parvb	parvin, beta	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20160804	MGI			
1322970	Parvb	parvin, beta	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20141003	MGI			
1322970	Parvb	parvin, beta	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1322970	Parvb	parvin, beta	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20141003	MGI			
1322970	Parvb	parvin, beta	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20141003	MGI			
1322970	Parvb	parvin, beta	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20160804	MGI			
1322970	Parvb	parvin, beta	gene	MP:0008211	decreased mature B cell number		IEA		N	RGD:5509061	20141003	MGI			
1322972	Plekho1	pleckstrin homology domain containing O1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641638
1322972	Plekho1	pleckstrin homology domain containing O1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641638
1322972	Plekho1	pleckstrin homology domain containing O1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641638
1322974	Dnah9	dynein, axonemal, heavy chain 9	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20210729	MGI			PMID:33347437
1322974	Dnah9	dynein, axonemal, heavy chain 9	gene	MP:0011059	abnormal ependyma motile cilium morphology		IAGP		N	RGD:5509061	20210729	MGI			PMID:33347437
1322978	Hinfp	histone H4 transcription factor	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590016
1322978	Hinfp	histone H4 transcription factor	gene	MP:0003695	delayed blastocyst hatching from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590016
1322978	Hinfp	histone H4 transcription factor	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590016
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000498	absent jejunum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000526	small inner medullary pyramid		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000526	small inner medullary pyramid		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14671317
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141204	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10903183
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044465
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20170309	MGI			PMID:26963625
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002163	abnormal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885021
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002294	short gestation period		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20170309	MGI			PMID:26963625
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003154	abnormal soft palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003158	dysphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10903183
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003568	uterus atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003572	abnormal uterus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003613	abnormal kidney medulla development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003613	abnormal kidney medulla development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003756	abnormal hard palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702402
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141204	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044465
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11044465
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885021
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004894	uterus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12468647
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0006320	abnormal interscapular fat pad morphology		IAGP		N	RGD:5509061	20170309	MGI			PMID:26963625
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0008794	increased lens epithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009709	hydrometra		IAGP		N	RGD:5509061	20141204	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009735	abnormal prostate gland development		IAGP		N	RGD:5509061	20141204	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885021
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16702402
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170309	MGI			PMID:26963625
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19276117
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737597
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9136926
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9925645
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011304	kidney papillary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885021
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0012503	increased midbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14671317
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0013317	abnormal seminal vesicle development		IAGP		N	RGD:5509061	20141204	MGI			PMID:10731669
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0015006	decreased fetal length		IAGP		N	RGD:5509061	20260611	MGI			PMID:9144284
1322981	Cdkn1c	cyclin dependent kinase inhibitor 1C	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:10731669
1322983	Cnot9	CCR4-NOT transcription complex, subunit 9	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1322983	Cnot9	CCR4-NOT transcription complex, subunit 9	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1322983	Cnot9	CCR4-NOT transcription complex, subunit 9	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1322983	Cnot9	CCR4-NOT transcription complex, subunit 9	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1322985	Spock1	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16806869
1322985	Spock1	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1322985	Spock1	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1322985	Spock1	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1322985	Spock1	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1322987	Stam2	signal transducing adaptor molecule (SH3 domain and ITAM motif) 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446783
1322987	Stam2	signal transducing adaptor molecule (SH3 domain and ITAM motif) 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22143071
1322987	Stam2	signal transducing adaptor molecule (SH3 domain and ITAM motif) 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446783
1322987	Stam2	signal transducing adaptor molecule (SH3 domain and ITAM motif) 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446783
1322987	Stam2	signal transducing adaptor molecule (SH3 domain and ITAM motif) 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446783
1322989	Slc25a17	solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20210422	MGI			PMID:32266253
1322989	Slc25a17	solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20210422	MGI			PMID:32266253
1322989	Slc25a17	solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:32266253
1322989	Slc25a17	solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:32266253
1322989	Slc25a17	solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:32266253
1322989	Slc25a17	solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210422	MGI			PMID:32266253
1322992	Igsf8	immunoglobulin superfamily, member 8	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1322994	Cacfd1	calcium channel flower domain containing 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22362363
1322994	Cacfd1	calcium channel flower domain containing 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20170323	MGI			
1322994	Cacfd1	calcium channel flower domain containing 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20170323	MGI			
1322994	Cacfd1	calcium channel flower domain containing 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22362363
1322994	Cacfd1	calcium channel flower domain containing 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20170323	MGI			
1322994	Cacfd1	calcium channel flower domain containing 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22362363
1322994	Cacfd1	calcium channel flower domain containing 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22362363
1322995	Ston2	stonin 2	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23345427
1322995	Ston2	stonin 2	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23345427
1322995	Ston2	stonin 2	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23345427
1322995	Ston2	stonin 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:23345427
1322995	Ston2	stonin 2	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:23345427
1322995	Ston2	stonin 2	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20141003	MGI			PMID:23345427
1322995	Ston2	stonin 2	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23345427
1322995	Ston2	stonin 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:23345427
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0000041	absent endolymphatic duct		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0003069	abnormal superior semicircular canal morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0003169	abnormal scala media morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701727
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0004369	absent utricle		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701727
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20180927	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0006013	absent endolymphatic sac		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591776
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701727
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20180215	MGI			PMID:29301908
1323001	Slc25a13	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	gene	MP:0030742	increased aspartic acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:17591776
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784089
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967219
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183592
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183592
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784089
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967219
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784089
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9593760
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183592
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784089
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784089
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11967219
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0003311	aminoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183592
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183592
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9593760
1323008	Inpp5b	inositol polyphosphate-5-phosphatase B	gene	MP:0011555	increased urine microglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21183592
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967868
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967868
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967868
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20241121	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541669
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967868
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541669
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967868
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541669
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967868
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541669
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20201002	MGI			PMID:32541879
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20220127	MGI			PMID:17967868
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541669
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0012117	decreased trophectoderm cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18541669
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0020364	abnormal female germ cell physiology		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220127	MGI			PMID:28506985
1323010	Kat8	K(lysine) acetyltransferase 8	gene	MP:0031474	increased female germ cell apoptosis		IAGP		N	RGD:5509061	20230615	MGI			PMID:28506985
1323014	Trim14	tripartite motif-containing 14	gene	MP:0003998	decreased thermal nociceptive threshold		IEA		N	RGD:5509061	20220519	MGI			
1323014	Trim14	tripartite motif-containing 14	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20191219	MGI			PMID:27666593
1323014	Trim14	tripartite motif-containing 14	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:27666593
1323014	Trim14	tripartite motif-containing 14	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:27666593
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201022	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20201022	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20181227	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20201231	MGI			
1323020	Rab3gap2	RAB3 GTPase activating protein subunit 2	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20181227	MGI			
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20190516	MGI			PMID:30087825
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190516	MGI			PMID:30087825
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20190516	MGI			PMID:30087825
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20190516	MGI			PMID:30087825
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20190516	MGI			PMID:30087825
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190516	MGI			PMID:30087825
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20190516	MGI			PMID:30087825
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20190516	MGI			PMID:30087825
1323024	Eif3e	eukaryotic translation initiation factor 3, subunit E	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20190516	MGI			PMID:30087825
1323026	Xpo5	exportin 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1323026	Xpo5	exportin 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1323026	Xpo5	exportin 5	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210826	MGI			
1323026	Xpo5	exportin 5	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210128	MGI			
1323026	Xpo5	exportin 5	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1323026	Xpo5	exportin 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1323026	Xpo5	exportin 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1323026	Xpo5	exportin 5	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1323026	Xpo5	exportin 5	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20210826	MGI			
1323026	Xpo5	exportin 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323026	Xpo5	exportin 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1323026	Xpo5	exportin 5	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1323027	Galnt9	polypeptide N-acetylgalactosaminyltransferase 9	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20220519	MGI			
1323030	Nup93	nucleoporin 93	gene	MP:0001714	absent trophoblast giant cells		IEA		N	RGD:5509061	20240926	MGI			
1323030	Nup93	nucleoporin 93	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240926	MGI			
1323030	Nup93	nucleoporin 93	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1323030	Nup93	nucleoporin 93	gene	MP:0004964	absent inner cell mass		IEA		N	RGD:5509061	20240926	MGI			
1323030	Nup93	nucleoporin 93	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1323030	Nup93	nucleoporin 93	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20221215	MGI			
1323037	Tmem108	transmembrane protein 108	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
1323037	Tmem108	transmembrane protein 108	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210826	MGI			
1323037	Tmem108	transmembrane protein 108	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0002635	reduced sensorimotor gating		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1323037	Tmem108	transmembrane protein 108	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1323037	Tmem108	transmembrane protein 108	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1323037	Tmem108	transmembrane protein 108	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0009938	abnormal hippocampus granule cell morphology		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1323037	Tmem108	transmembrane protein 108	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1323037	Tmem108	transmembrane protein 108	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323037	Tmem108	transmembrane protein 108	gene	MP:0020335	abnormal dentate gyrus neuron dendrite morphology		IAGP		N	RGD:5509061	20170413	MGI			PMID:28096412
1323043	Depdc5	DEP domain containing 5	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1323043	Depdc5	DEP domain containing 5	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1323043	Depdc5	DEP domain containing 5	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20160421	MGI			
1323043	Depdc5	DEP domain containing 5	gene	MP:0005603	neuron hypertrophy		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20180524	MGI			PMID:29274432
1323043	Depdc5	DEP domain containing 5	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1323043	Depdc5	DEP domain containing 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323050	Ints9	integrator complex subunit 9	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1323050	Ints9	integrator complex subunit 9	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1323050	Ints9	integrator complex subunit 9	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1323050	Ints9	integrator complex subunit 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323052	Rae1	ribonucleic acid export 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1323052	Rae1	ribonucleic acid export 1	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20191205	MGI			PMID:26731471
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20191205	MGI			PMID:26731471
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1323052	Rae1	ribonucleic acid export 1	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1323052	Rae1	ribonucleic acid export 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0008007	abnormal cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:26731471
1323052	Rae1	ribonucleic acid export 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16476774
1323052	Rae1	ribonucleic acid export 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12551952
1323052	Rae1	ribonucleic acid export 1	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:16476774
1323054	Mmp17	matrix metallopeptidase 17	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1323054	Mmp17	matrix metallopeptidase 17	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347258
1323054	Mmp17	matrix metallopeptidase 17	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347258
1323054	Mmp17	matrix metallopeptidase 17	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347258
1323054	Mmp17	matrix metallopeptidase 17	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347258
1323054	Mmp17	matrix metallopeptidase 17	gene	MP:0010981	abnormal branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347258
1323054	Mmp17	matrix metallopeptidase 17	gene	MP:0011737	hypodipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347258
1323054	Mmp17	matrix metallopeptidase 17	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21347258
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9878048
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393958
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0008129	absent brain internal capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393958
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0009026	abnormal brain pia mater morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0009027	abnormal subarachnoid space morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0009586	increased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9878048
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0011724	ectopic cortical neuron		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1323056	Vasp	vasodilator-stimulated phosphoprotein	gene	MP:0014697	abnormal fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:22908313
1323059	Fam89b	family with sequence similarity 89, member B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000322	increased granulocyte number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000341	abnormal bile color		IAGP		N	RGD:5509061	20200116	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000552	abnormal radius morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20201022	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0002187	abnormal fibula morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0003947	abnormal cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20200116	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0004974	decreased regulatory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005084	abnormal gallbladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005108	abnormal ulna morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005270	abnormal zygomatic bone morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005415	intrahepatic cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008173	increased follicular B cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008178	decreased germinal center B cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008347	decreased gamma-delta T cell number		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008524	increased plasmacytoid dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0009109	decreased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0009303	decreased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0009342	enlarged gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0009492	abnormal gallbladder epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0010099	abnormal thoracic cage shape		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0011016	increased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0011234	abnormal retinol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0011504	abnormal limb long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0012288	abnormal paradoxical sleep pattern		IAGP		N	RGD:5509061	20161124	MGI			PMID:27806374
1323064	Sik3	SIK family kinase 3	gene	MP:0012289	abnormal non-rapid eye movement sleep pattern		IAGP		N	RGD:5509061	20161124	MGI			PMID:27806374
1323064	Sik3	SIK family kinase 3	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0012768	decreased KLRG1-positive NK cell number		IEA		N	RGD:5509061	20181227	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013154	increased KLRG1+ CD8-positive alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013418	increased memory-marker gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013420	decreased CD5-positive gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013427	increased memory-marker NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013433	increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013511	increased CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013513	decreased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013517	increased KLRG1-positive CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013519	decreased CD4-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013522	decreased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013675	decreased Ly6C-positive mature NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013679	increased Ly6C-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013683	decreased early germinal center B cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013774	decreased KLRG1-positive T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0013775	increased KLRG1-positive T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1323064	Sik3	SIK family kinase 3	gene	MP:0014624	abnormal brain delta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:27806374
1323064	Sik3	SIK family kinase 3	gene	MP:0014638	increased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:27806374
1323064	Sik3	SIK family kinase 3	gene	MP:0014682	increased polyploid hepatocyte number		IAGP		N	RGD:5509061	20250703	MGI			PMID:22662228
1323064	Sik3	SIK family kinase 3	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20171012	MGI			PMID:27806374
1323064	Sik3	SIK family kinase 3	gene	MP:0030388	large fontanelles		IAGP		N	RGD:5509061	20171207	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0030884	rachitic rosary		IAGP		N	RGD:5509061	20181101	MGI			PMID:22318228
1323064	Sik3	SIK family kinase 3	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:22662228
1323069	Amfr	autocrine motility factor receptor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:25789613
1323069	Amfr	autocrine motility factor receptor	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:25789613
1323069	Amfr	autocrine motility factor receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20160107	MGI			PMID:25789613
1323069	Amfr	autocrine motility factor receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20160107	MGI			PMID:25789613
1323069	Amfr	autocrine motility factor receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160107	MGI			PMID:25789613
1323069	Amfr	autocrine motility factor receptor	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1323069	Amfr	autocrine motility factor receptor	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1323069	Amfr	autocrine motility factor receptor	gene	MP:0003046	liver cirrhosis		IAGP		N	RGD:5509061	20160107	MGI			PMID:25789613
1323069	Amfr	autocrine motility factor receptor	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20160107	MGI			PMID:25789613
1323069	Amfr	autocrine motility factor receptor	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1323069	Amfr	autocrine motility factor receptor	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1323069	Amfr	autocrine motility factor receptor	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1323069	Amfr	autocrine motility factor receptor	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20160107	MGI			PMID:25789613
1323069	Amfr	autocrine motility factor receptor	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20160107	MGI			PMID:25789613
1323069	Amfr	autocrine motility factor receptor	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1323076	Usp28	ubiquitin specific peptidase 28	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20151210	MGI			PMID:24687851
1323076	Usp28	ubiquitin specific peptidase 28	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20151210	MGI			PMID:24687851
1323076	Usp28	ubiquitin specific peptidase 28	gene	MP:0005380	embryo phenotype		IAGP		N	RGD:5509061	20250918	MGI			PMID:38407237
1323076	Usp28	ubiquitin specific peptidase 28	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20151210	MGI			PMID:24687851
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323078	Vps18	VPS18 CORVET/HOPS core subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22854957
1323080	Rnf25	ring finger protein 25	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1323080	Rnf25	ring finger protein 25	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20160421	MGI			
1323080	Rnf25	ring finger protein 25	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20181227	MGI			
1323080	Rnf25	ring finger protein 25	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1323080	Rnf25	ring finger protein 25	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20201022	MGI			
1323080	Rnf25	ring finger protein 25	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20170105	MGI			
1323080	Rnf25	ring finger protein 25	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1323080	Rnf25	ring finger protein 25	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1323081	Shtn1	shootin 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30082022
1323081	Shtn1	shootin 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20190919	MGI			PMID:30082022
1323081	Shtn1	shootin 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30082022
1323081	Shtn1	shootin 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1323081	Shtn1	shootin 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1323081	Shtn1	shootin 1	gene	MP:0008222	decreased hippocampal commissure size		IAGP		N	RGD:5509061	20190919	MGI			PMID:30082022
1323081	Shtn1	shootin 1	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30082022
1323081	Shtn1	shootin 1	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20190919	MGI			PMID:30082022
1323081	Shtn1	shootin 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30082022
1323081	Shtn1	shootin 1	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20190919	MGI			PMID:30082022
1323081	Shtn1	shootin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:30082022
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20220811	MGI			
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20220519	MGI			
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20220519	MGI			
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20210415	MGI			PMID:32272552
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0009619	abnormal optokinetic reflex		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0010452	retina microaneurysm		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323084	Dhdds	dehydrodolichyl diphosphate synthase	gene	MP:0031141	increased retina vascular tortuosity		IAGP		N	RGD:5509061	20210506	MGI			PMID:32245241
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0003742	narrow head		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0004576	abnormal embryonic autopod plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0011261	abnormal limb mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:25251415
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:21750036
1323088	2700049A03Rik	RIKEN cDNA 2700049A03 gene	gene	MP:0031682	abnormal centriole morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:25251415
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0001787	pericardial edema		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20220519	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0012270	cardiac edema		IEA		N	RGD:5509061	20251211	MGI			
1323089	Stt3b	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220811	MGI			
1323094	Cdc42ep4	CDC42 effector protein 4	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20171012	MGI			PMID:26657011
1323094	Cdc42ep4	CDC42 effector protein 4	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20171012	MGI			PMID:26657011
1323094	Cdc42ep4	CDC42 effector protein 4	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20171012	MGI			PMID:26657011
1323094	Cdc42ep4	CDC42 effector protein 4	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20171012	MGI			PMID:26657011
1323094	Cdc42ep4	CDC42 effector protein 4	gene	MP:0011002	enhanced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20171012	MGI			PMID:26657011
1323094	Cdc42ep4	CDC42 effector protein 4	gene	MP:0011273	prolonged excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20171012	MGI			PMID:26657011
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021016
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021016
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17357084
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17357084
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17357084
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021016
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021016
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021016
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021016
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17021016
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1323100	Dgkd	diacylglycerol kinase, delta	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1323103	Mmp28	matrix metallopeptidase 28 (epilysin)	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265166
1323103	Mmp28	matrix metallopeptidase 28 (epilysin)	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265166
1323103	Mmp28	matrix metallopeptidase 28 (epilysin)	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265166
1323103	Mmp28	matrix metallopeptidase 28 (epilysin)	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265166
1323103	Mmp28	matrix metallopeptidase 28 (epilysin)	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265166
1323103	Mmp28	matrix metallopeptidase 28 (epilysin)	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265166
1323103	Mmp28	matrix metallopeptidase 28 (epilysin)	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19265166
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0000467	abnormal esophagus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0000648	absent sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0000763	abnormal filiform papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0003155	abnormal telomere length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0003751	oral leukoplakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596237
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19679647
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944479
1323105	Terf1	telomeric repeat binding factor 1	gene	MP:0030926	increased skin pigmentation		IAGP		N	RGD:5509061	20190117	MGI			PMID:19679647
1323106	Cracd	capping protein inhibiting regulator of actin	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20201022	MGI			
1323106	Cracd	capping protein inhibiting regulator of actin	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1323110	Ndufaf7	NADH:ubiquinone oxidoreductase complex assembly factor 7	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20141218	MGI			PMID:24838397
1323112	E2f4	E2F transcription factor 4	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0000346	broad head		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0001400	hyperresponsive		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0001867	rhinitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160218	MGI			PMID:26825228
1323112	E2f4	E2F transcription factor 4	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
1323112	E2f4	E2F transcription factor 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
1323112	E2f4	E2F transcription factor 4	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160218	MGI			PMID:26825228
1323112	E2f4	E2F transcription factor 4	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0002244	abnormal turbinate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
1323112	E2f4	E2F transcription factor 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26825228
1323112	E2f4	E2F transcription factor 4	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11030352
1323112	E2f4	E2F transcription factor 4	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0004728	abnormal efferent ductules of testis morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26825228
1323112	E2f4	E2F transcription factor 4	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0006423	dilated rete testis		IAGP		N	RGD:5509061	20160218	MGI			PMID:26825228
1323112	E2f4	E2F transcription factor 4	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0008142	decreased small intestinal villus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0009257	dilated seminiferous tubule		IAGP		N	RGD:5509061	20160218	MGI			PMID:26825228
1323112	E2f4	E2F transcription factor 4	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0010178	increased number of Howell-Jolly bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0010178	increased number of Howell-Jolly bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0010316	increased thyroid tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
1323112	E2f4	E2F transcription factor 4	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498715
1323112	E2f4	E2F transcription factor 4	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:28675157
1323112	E2f4	E2F transcription factor 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11030352
1323112	E2f4	E2F transcription factor 4	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26825228
1323112	E2f4	E2F transcription factor 4	gene	MP:0013792	abnormal small intestine goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:10983977
1323112	E2f4	E2F transcription factor 4	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:10983976
1323112	E2f4	E2F transcription factor 4	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20210805	MGI			PMID:10983976
1323114	Zbtb48	zinc finger and BTB domain containing 48	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1323114	Zbtb48	zinc finger and BTB domain containing 48	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210520	MGI			
1323114	Zbtb48	zinc finger and BTB domain containing 48	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1323114	Zbtb48	zinc finger and BTB domain containing 48	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1323116	Ubn1	ubinuclein 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1323116	Ubn1	ubinuclein 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1323116	Ubn1	ubinuclein 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20181227	MGI			
1323116	Ubn1	ubinuclein 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1323116	Ubn1	ubinuclein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1323116	Ubn1	ubinuclein 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1323116	Ubn1	ubinuclein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1323116	Ubn1	ubinuclein 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1323116	Ubn1	ubinuclein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1323116	Ubn1	ubinuclein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323118	Tead3	TEA domain family member 3	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20181227	MGI			
1323118	Tead3	TEA domain family member 3	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1323118	Tead3	TEA domain family member 3	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20181227	MGI			
1323118	Tead3	TEA domain family member 3	gene	MP:0010869	decreased bone trabecula number		IEA		N	RGD:5509061	20210128	MGI			
1323118	Tead3	TEA domain family member 3	gene	MP:0013630	increased bone trabecular spacing		IEA		N	RGD:5509061	20211021	MGI			
1323119	Stap1	signal transducing adaptor family member 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1323119	Stap1	signal transducing adaptor family member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200903	MGI			PMID:31996024
1323121	Vrk2	vaccinia related kinase 2	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20240307	MGI			PMID:37452335
1323121	Vrk2	vaccinia related kinase 2	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:37452335
1323121	Vrk2	vaccinia related kinase 2	gene	MP:0020512	abnormal dendritic mushroom spine morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:37452335
1323121	Vrk2	vaccinia related kinase 2	gene	MP:0020514	abnormal dendritic thin spine morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:37452335
1323121	Vrk2	vaccinia related kinase 2	gene	MP:0021010	impaired synaptic physiology		IAGP		N	RGD:5509061	20240307	MGI			PMID:37452335
1323123	Ptpn18	protein tyrosine phosphatase, non-receptor type 18	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1323123	Ptpn18	protein tyrosine phosphatase, non-receptor type 18	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1323123	Ptpn18	protein tyrosine phosphatase, non-receptor type 18	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1323123	Ptpn18	protein tyrosine phosphatase, non-receptor type 18	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1323123	Ptpn18	protein tyrosine phosphatase, non-receptor type 18	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220519	MGI			
1323123	Ptpn18	protein tyrosine phosphatase, non-receptor type 18	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20250508	MGI			
1323123	Ptpn18	protein tyrosine phosphatase, non-receptor type 18	gene	MP:0006241	abnormal placement of pupils		IEA		N	RGD:5509061	20231207	MGI			
1323123	Ptpn18	protein tyrosine phosphatase, non-receptor type 18	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220519	MGI			
1323123	Ptpn18	protein tyrosine phosphatase, non-receptor type 18	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1323126	Riok2	RIO kinase 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1323126	Riok2	RIO kinase 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1323126	Riok2	RIO kinase 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20231207	MGI			
1323126	Riok2	RIO kinase 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0008588	abnormal circulating interleukin level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323126	Riok2	RIO kinase 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323126	Riok2	RIO kinase 2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1323126	Riok2	RIO kinase 2	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1323126	Riok2	RIO kinase 2	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:33753942
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200209
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200209
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200209
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200209
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368888
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200209
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083848
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200209
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368888
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16200209
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368888
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083848
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083848
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201002	MGI			PMID:18083848
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200924	MGI			PMID:19109562
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:18083848
1323133	Adamts13	ADAM metallopeptidase with thrombospondin type 1 motif 13	gene	MP:0031165	increased circulating von Willebrand factor level		IAGP		N	RGD:5509061	20201015	MGI			PMID:16200209
1323135	Brd10	bromodomain containing 10	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1323135	Brd10	bromodomain containing 10	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1323135	Brd10	bromodomain containing 10	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1323135	Brd10	bromodomain containing 10	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1323135	Brd10	bromodomain containing 10	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0004246	abnormal extensor digitorum longus morphology		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323137	Mybpc2	myosin binding protein C, fast-type	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20240718	MGI			PMID:33888578
1323139	Cers5	ceramide synthase 5	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210520	MGI			
1323139	Cers5	ceramide synthase 5	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20241219	MGI			PMID:37216827
1323139	Cers5	ceramide synthase 5	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1323139	Cers5	ceramide synthase 5	gene	MP:0001516	abnormal motor coordination/balance		IEA		N	RGD:5509061	20201231	MGI			
1323139	Cers5	ceramide synthase 5	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20241219	MGI			PMID:37216827
1323139	Cers5	ceramide synthase 5	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201022	MGI			
1323139	Cers5	ceramide synthase 5	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20241219	MGI			PMID:37216827
1323139	Cers5	ceramide synthase 5	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20241219	MGI			PMID:37216827
1323139	Cers5	ceramide synthase 5	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1323139	Cers5	ceramide synthase 5	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1323139	Cers5	ceramide synthase 5	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220811	MGI			
1323141	Sin3a	SIN3 transcription regulator family member A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998811
1323141	Sin3a	SIN3 transcription regulator family member A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15998811
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407208
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407208
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407208
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20160929	MGI			PMID:24557352
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407208
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407208
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20160929	MGI			PMID:24557352
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0002546	mydriasis		IEA		N	RGD:5509061	20181227	MGI			
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407208
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713727
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20160929	MGI			PMID:24557352
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20160929	MGI			PMID:24557352
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20160929	MGI			PMID:24557352
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407208
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20160929	MGI			PMID:24557352
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20160929	MGI			PMID:24557352
1323142	Lpcat1	lysophosphatidylcholine acyltransferase 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20160929	MGI			PMID:24557352
1323143	Zfp474	zinc finger protein 474	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1323143	Zfp474	zinc finger protein 474	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1323143	Zfp474	zinc finger protein 474	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1323143	Zfp474	zinc finger protein 474	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1323143	Zfp474	zinc finger protein 474	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210520	MGI			
1323143	Zfp474	zinc finger protein 474	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1323143	Zfp474	zinc finger protein 474	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20210520	MGI			
1323143	Zfp474	zinc finger protein 474	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20210520	MGI			
1323143	Zfp474	zinc finger protein 474	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1323143	Zfp474	zinc finger protein 474	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210520	MGI			
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363972
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363972
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20231207	MGI			
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20260402	MGI			
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363972
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0008691	decreased interleukin-23 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363972
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363972
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363972
1323144	Fastk	Fas-activated serine/threonine kinase	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363972
1323146	Bpifb6	BPI fold containing family B, member 6	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20241121	MGI			
1323146	Bpifb6	BPI fold containing family B, member 6	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20250508	MGI			
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0000525	renal tubular acidosis		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0000533	kidney hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0002318	hypercapnia		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0002986	decreased urine calcium level		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20160707	MGI			PMID:22045552
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0005488	bronchial epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0005576	decreased pulmonary ventilation		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20160707	MGI			PMID:22045552
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0008816	petechiae		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20160707	MGI			PMID:22045552
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0011428	decreased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0011437	glomerulus hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145776
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0011470	increased urine creatinine level		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0011735	increased urine ammonia level		IAGP		N	RGD:5509061	20160707	MGI			PMID:26068853
1323149	Gpr4	G protein-coupled receptor 4	gene	MP:0014273	abnormal skin vasculature morphology		IAGP		N	RGD:5509061	20230810	MGI			PMID:17145776
1323151	Atraid	all-trans retinoic acid induced differentiation factor	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20141003	MGI			
1323154	Mcrs1	microspherule protein 1	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20240613	MGI			PMID:31671403
1323154	Mcrs1	microspherule protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160818	MGI			PMID:25816988
1323154	Mcrs1	microspherule protein 1	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:31671403
1323154	Mcrs1	microspherule protein 1	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20220519	MGI			
1323154	Mcrs1	microspherule protein 1	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:31671403
1323154	Mcrs1	microspherule protein 1	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20240801	MGI			PMID:31671403
1323154	Mcrs1	microspherule protein 1	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:31671403
1323154	Mcrs1	microspherule protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160818	MGI			PMID:25816988
1323154	Mcrs1	microspherule protein 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20240801	MGI			PMID:31671403
1323154	Mcrs1	microspherule protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323154	Mcrs1	microspherule protein 1	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20240801	MGI			PMID:31671403
1323154	Mcrs1	microspherule protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323156	Taf6	TATA-box binding protein associated factor 6	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1323156	Taf6	TATA-box binding protein associated factor 6	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1323156	Taf6	TATA-box binding protein associated factor 6	gene	MP:0006204	embryonic lethality before implantation		IEA		N	RGD:5509061	20111116	MGI			
1323156	Taf6	TATA-box binding protein associated factor 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323156	Taf6	TATA-box binding protein associated factor 6	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1323156	Taf6	TATA-box binding protein associated factor 6	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323158	Hsph1	heat shock 105kDa/110kDa protein 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20150917	MGI			PMID:18658041
1323158	Hsph1	heat shock 105kDa/110kDa protein 1	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20150917	MGI			PMID:18658041
1323158	Hsph1	heat shock 105kDa/110kDa protein 1	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20150917	MGI			PMID:18658041
1323160	Cd22	CD22 antigen	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864124
1323160	Cd22	CD22 antigen	gene	MP:0001800	abnormal humoral immune response		IEA		N	RGD:5509061	20111116	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0001802	arrested B cell differentiation		IEA		N	RGD:5509061	20111116	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1323160	Cd22	CD22 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967951
1323160	Cd22	CD22 antigen	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209047
1323160	Cd22	CD22 antigen	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1323160	Cd22	CD22 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22965838
1323160	Cd22	CD22 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864124
1323160	Cd22	CD22 antigen	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209047
1323160	Cd22	CD22 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864124
1323160	Cd22	CD22 antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9586639
1323160	Cd22	CD22 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209047
1323160	Cd22	CD22 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864124
1323160	Cd22	CD22 antigen	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420268
1323160	Cd22	CD22 antigen	gene	MP:0004944	abnormal B cell negative selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9586639
1323160	Cd22	CD22 antigen	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864124
1323160	Cd22	CD22 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15378059
1323160	Cd22	CD22 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22965838
1323160	Cd22	CD22 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24344237
1323160	Cd22	CD22 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15378059
1323160	Cd22	CD22 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24344237
1323160	Cd22	CD22 antigen	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354178
1323160	Cd22	CD22 antigen	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967951
1323160	Cd22	CD22 antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15378059
1323160	Cd22	CD22 antigen	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IEA		N	RGD:5509061	20141225	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0008167	increased B-1a cell number		IEA		N	RGD:5509061	20150507	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420268
1323160	Cd22	CD22 antigen	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864124
1323160	Cd22	CD22 antigen	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967951
1323160	Cd22	CD22 antigen	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9586639
1323160	Cd22	CD22 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15378059
1323160	Cd22	CD22 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420268
1323160	Cd22	CD22 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354178
1323160	Cd22	CD22 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22965838
1323160	Cd22	CD22 antigen	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0008188	abnormal transitional stage B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354178
1323160	Cd22	CD22 antigen	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20151015	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15378059
1323160	Cd22	CD22 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420268
1323160	Cd22	CD22 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354178
1323160	Cd22	CD22 antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967951
1323160	Cd22	CD22 antigen	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420268
1323160	Cd22	CD22 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8864124
1323160	Cd22	CD22 antigen	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967951
1323160	Cd22	CD22 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967951
1323160	Cd22	CD22 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967951
1323160	Cd22	CD22 antigen	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209047
1323160	Cd22	CD22 antigen	gene	MP:0008729	decreased memory B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8967951
1323160	Cd22	CD22 antigen	gene	MP:0008746	abnormal peripheral B cell anergy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24344237
1323160	Cd22	CD22 antigen	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354178
1323160	Cd22	CD22 antigen	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22965838
1323160	Cd22	CD22 antigen	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22965838
1323160	Cd22	CD22 antigen	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20180215	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0010674	increased activation-induced B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24344237
1323160	Cd22	CD22 antigen	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20180215	MGI			
1323160	Cd22	CD22 antigen	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836650
1323160	Cd22	CD22 antigen	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:22965838
1323160	Cd22	CD22 antigen	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:8864124
1323160	Cd22	CD22 antigen	gene	MP:0014472	impaired B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:22965838
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20231207	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20111116	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20111116	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20230601	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20231207	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20231207	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20231207	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20191114	MGI			PMID:29079736
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20231207	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20231207	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:29079736
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0008911	induced hyperactivity		IEA		N	RGD:5509061	20111116	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1323162	Cars2	cysteinyl-tRNA synthetase 2, mitochondrial	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20231207	MGI			
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20160811	MGI			
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811152
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811152
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811152
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811152
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811152
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811152
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811152
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0009488	abnormal pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811152
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20231207	MGI			
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20160421	MGI			
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:27930311
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811152
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1323164	Spop	speckle-type BTB/POZ protein	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20201022	MGI			
1323168	Khdc3	KH domain containing 3, subcortical maternal complex member	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19376971
1323168	Khdc3	KH domain containing 3, subcortical maternal complex member	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19376971
1323168	Khdc3	KH domain containing 3, subcortical maternal complex member	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19376971
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16547221
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0000350	abnormal cell proliferation		IEA		N	RGD:5509061	20161201	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584150
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416854
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777721
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16547221
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055226
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777721
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777721
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777721
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16547221
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213685
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777721
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777721
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213685
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777721
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IEA		N	RGD:5509061	20161201	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16547221
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008036	abnormal NK T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193707
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12193707
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213685
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055226
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8777721
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584150
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345221
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055226
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880398
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880398
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10213685
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416854
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008343	abnormal gamma-delta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416854
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008353	increased mature gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416854
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16860759
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345221
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416854
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416854
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345221
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416854
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19009524
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584150
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416854
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345221
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15345221
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880398
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20180215	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0010839	decreased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20180215	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0011822	increased CD8-positive, alpha-beta memory T cell proliferation		IEA		N	RGD:5509061	20161201	MGI			
1323170	Itk	IL2 inducible T cell kinase	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20180215	MGI			
1323171	Dnhd1	dynein heavy chain domain 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220317	MGI			PMID:34932939
1323171	Dnhd1	dynein heavy chain domain 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220317	MGI			PMID:34932939
1323171	Dnhd1	dynein heavy chain domain 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220317	MGI			PMID:34932939
1323171	Dnhd1	dynein heavy chain domain 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220317	MGI			PMID:34932939
1323171	Dnhd1	dynein heavy chain domain 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:34932939
1323171	Dnhd1	dynein heavy chain domain 1	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20220317	MGI			PMID:34932939
1323171	Dnhd1	dynein heavy chain domain 1	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220317	MGI			PMID:34932939
1323171	Dnhd1	dynein heavy chain domain 1	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20220317	MGI			PMID:34932939
1323171	Dnhd1	dynein heavy chain domain 1	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220317	MGI			PMID:34932939
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20180215	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518968
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518968
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518968
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518968
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0001606	impaired hematopoiesis		IEA		N	RGD:5509061	20151126	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0001790	abnormal immune system physiology		IEA		N	RGD:5509061	20141003	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518968
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157938
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871644
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871644
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20161201	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002619	abnormal lymphocyte morphology		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002634	abnormal sensorimotor gating		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0002895	abnormal otolithic membrane morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157938
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518968
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IEA		N	RGD:5509061	20141003	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157938
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157938
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871644
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005425	increased macrophage cell number		IEA		N	RGD:5509061	20180215	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20250508	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20170622	MGI			PMID:17420276
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008037	abnormal T cell morphology		IEA		N	RGD:5509061	20141003	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20180215	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20111116	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IEA		N	RGD:5509061	20141003	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008077	abnormal CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190613	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20151126	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20111116	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20141003	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008082	increased single-positive T cell number		IEA		N	RGD:5509061	20151126	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20151126	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518968
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008169	increased B-1b cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008170	decreased B-1b cell number		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518968
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:27210752
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157938
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20170622	MGI			PMID:19103880
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943182
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22431588
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157938
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:27210752
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190411	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20161201	MGI			
1323175	Dock2	dedicator of cyto-kinesis 2	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:19103880
1323178	Btbd3	BTB domain containing 3	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20200514	MGI			
1323178	Btbd3	BTB domain containing 3	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20200514	MGI			
1323178	Btbd3	BTB domain containing 3	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20241121	MGI			
1323178	Btbd3	BTB domain containing 3	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20200813	MGI			PMID:31501410
1323178	Btbd3	BTB domain containing 3	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20200813	MGI			PMID:31501410
1323178	Btbd3	BTB domain containing 3	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20200813	MGI			PMID:31501410
1323178	Btbd3	BTB domain containing 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20200813	MGI			PMID:31501410
1323178	Btbd3	BTB domain containing 3	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20200813	MGI			PMID:31501410
1323178	Btbd3	BTB domain containing 3	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20200514	MGI			
1323178	Btbd3	BTB domain containing 3	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20200514	MGI			
1323178	Btbd3	BTB domain containing 3	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1323178	Btbd3	BTB domain containing 3	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20220421	MGI			PMID:31501410
1323178	Btbd3	BTB domain containing 3	gene	MP:0013890	increased CD8-positive, CD25-positive alpha-beta T cell number		IEA		N	RGD:5509061	20220519	MGI			
1323178	Btbd3	BTB domain containing 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:31501410
1323179	Setd1a	SET domain containing 1A	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1323179	Setd1a	SET domain containing 1A	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1323179	Setd1a	SET domain containing 1A	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1323179	Setd1a	SET domain containing 1A	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
1323179	Setd1a	SET domain containing 1A	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550110
1323179	Setd1a	SET domain containing 1A	gene	MP:0002635	reduced sensorimotor gating		IAGP		N	RGD:5509061	20221117	MGI			PMID:35245111
1323179	Setd1a	SET domain containing 1A	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1323179	Setd1a	SET domain containing 1A	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1323179	Setd1a	SET domain containing 1A	gene	MP:0003345	decreased rib number		IEA		N	RGD:5509061	20160804	MGI			
1323179	Setd1a	SET domain containing 1A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550110
1323179	Setd1a	SET domain containing 1A	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1323179	Setd1a	SET domain containing 1A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550110
1323179	Setd1a	SET domain containing 1A	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550110
1323179	Setd1a	SET domain containing 1A	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20221117	MGI			PMID:35245111
1323179	Setd1a	SET domain containing 1A	gene	MP:0009710	anhedonia		IAGP		N	RGD:5509061	20221117	MGI			PMID:35245111
1323179	Setd1a	SET domain containing 1A	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1323179	Setd1a	SET domain containing 1A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550110
1323179	Setd1a	SET domain containing 1A	gene	MP:0020379	abnormal sucrose solution preference		IAGP		N	RGD:5509061	20221117	MGI			PMID:35245111
1323179	Setd1a	SET domain containing 1A	gene	MP:0020421	increased freezing behavior		IAGP		N	RGD:5509061	20221117	MGI			PMID:35245111
1323179	Setd1a	SET domain containing 1A	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20221117	MGI			PMID:35245111
1323179	Setd1a	SET domain containing 1A	gene	MP:0021090	abnormal dendrite arborization pattern		IAGP		N	RGD:5509061	20221117	MGI			PMID:35245111
1323179	Setd1a	SET domain containing 1A	gene	MP:0030950	abnormal synaptic vesicle exocytosis		IAGP		N	RGD:5509061	20221117	MGI			PMID:35245111
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873190
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873190
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288583
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873190
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288583
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873190
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0008112	abnormal monocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0008389	hypochromic macrocytic anemia		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873190
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0010129	increased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803851
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288583
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723201
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0011181	increased hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723200
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0013771	decreased effector memory T-helper cell number		IAGP		N	RGD:5509061	20230316	MGI			PMID:35304452
1323180	Tet2	tet methylcytosine dioxygenase 2	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260611	MGI			PMID:27622333
1323182	Ube2k	ubiquitin-conjugating enzyme E2K	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18710920
1323187	Dapk1	death associated protein kinase 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18806755
1323187	Dapk1	death associated protein kinase 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160421	MGI			
1323187	Dapk1	death associated protein kinase 1	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20141836
1323187	Dapk1	death associated protein kinase 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18806755
1323187	Dapk1	death associated protein kinase 1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20141836
1323187	Dapk1	death associated protein kinase 1	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20141836
1323187	Dapk1	death associated protein kinase 1	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:20141836
1323187	Dapk1	death associated protein kinase 1	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18806755
1323187	Dapk1	death associated protein kinase 1	gene	MP:0011372	decreased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15010850
1323187	Dapk1	death associated protein kinase 1	gene	MP:0011372	decreased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18806755
1323194	Slc7a13	solute carrier family 7, (cationic amino acid transporter, y+ system) member 13	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20211021	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20160811	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20160811	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20160811	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20160811	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220519	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20160811	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20160811	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20160811	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20160421	MGI			
1323195	Anapc15	anaphase promoting complex C subunit 15	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20160811	MGI			
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20141003	MGI			
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20160804	MGI			
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0004647	decreased lumbar vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0008409	increased cellular sensitivity to hydroxyurea induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20141003	MGI			
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323199	Kmt5b	lysine methyltransferase 5B	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18676810
1323204	Cep290	centrosomal protein 290	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0000542	left-sided isomerism		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0000694	spleen hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1323204	Cep290	centrosomal protein 290	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1323204	Cep290	centrosomal protein 290	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1323204	Cep290	centrosomal protein 290	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16632484
1323204	Cep290	centrosomal protein 290	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1323204	Cep290	centrosomal protein 290	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111124	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20111124	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24223178
1323204	Cep290	centrosomal protein 290	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20160519	MGI			PMID:26301811
1323204	Cep290	centrosomal protein 290	gene	MP:0003342	accessory spleen		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20210128	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16632484
1323204	Cep290	centrosomal protein 290	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16632484
1323204	Cep290	centrosomal protein 290	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0004512	anosmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898177
1323204	Cep290	centrosomal protein 290	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:16632484
1323204	Cep290	centrosomal protein 290	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20160519	MGI			PMID:26301811
1323204	Cep290	centrosomal protein 290	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200206	MGI			PMID:29899041
1323204	Cep290	centrosomal protein 290	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0008489	slow postnatal weight gain		IEA		N	RGD:5509061	20111124	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16632484
1323204	Cep290	centrosomal protein 290	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16632484
1323204	Cep290	centrosomal protein 290	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21245082
1323204	Cep290	centrosomal protein 290	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898177
1323204	Cep290	centrosomal protein 290	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1323204	Cep290	centrosomal protein 290	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0010403	atrial septal defect		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0010419	inlet ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20160519	MGI			PMID:26301811
1323204	Cep290	centrosomal protein 290	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160304	MGI			PMID:24946806
1323204	Cep290	centrosomal protein 290	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20210128	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0011665	d-loop transposition of the great arteries		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0011682	renal glomerulus cyst		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20141003	MGI			
1323204	Cep290	centrosomal protein 290	gene	MP:0012671	retina spots		IAGP		N	RGD:5509061	20150416	MGI			PMID:16632484
1323204	Cep290	centrosomal protein 290	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:24051377
1323204	Cep290	centrosomal protein 290	gene	MP:0020384	absent kidney epithelial cell primary cilium		IAGP		N	RGD:5509061	20161013	MGI			PMID:26301811
1323204	Cep290	centrosomal protein 290	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:24946806
1323207	Dbndd2	dysbindin domain containing 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20160811	MGI			
1323207	Dbndd2	dysbindin domain containing 2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
1323207	Dbndd2	dysbindin domain containing 2	gene	MP:0004930	small epididymis		IEA		N	RGD:5509061	20160811	MGI			
1323207	Dbndd2	dysbindin domain containing 2	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20211021	MGI			
1323207	Dbndd2	dysbindin domain containing 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1323207	Dbndd2	dysbindin domain containing 2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20160811	MGI			
1323211	Enpp6	ectonucleotide pyrophosphatase/phosphodiesterase 6	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20250911	MGI			PMID:26888014
1323211	Enpp6	ectonucleotide pyrophosphatase/phosphodiesterase 6	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:26888014
1323211	Enpp6	ectonucleotide pyrophosphatase/phosphodiesterase 6	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20250911	MGI			PMID:26888014
1323211	Enpp6	ectonucleotide pyrophosphatase/phosphodiesterase 6	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:26888014
1323211	Enpp6	ectonucleotide pyrophosphatase/phosphodiesterase 6	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20250911	MGI			PMID:26888014
1323211	Enpp6	ectonucleotide pyrophosphatase/phosphodiesterase 6	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20250911	MGI			PMID:26888014
1323211	Enpp6	ectonucleotide pyrophosphatase/phosphodiesterase 6	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20250911	MGI			PMID:26888014
1323211	Enpp6	ectonucleotide pyrophosphatase/phosphodiesterase 6	gene	MP:0021131	increased glycerophosphocholine level		IAGP		N	RGD:5509061	20250911	MGI			PMID:26888014
1323211	Enpp6	ectonucleotide pyrophosphatase/phosphodiesterase 6	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20250911	MGI			PMID:26888014
1323213	Sart3	squamous cell carcinoma antigen recognized by T cells 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1323213	Sart3	squamous cell carcinoma antigen recognized by T cells 3	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1323213	Sart3	squamous cell carcinoma antigen recognized by T cells 3	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21447833
1323213	Sart3	squamous cell carcinoma antigen recognized by T cells 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1323213	Sart3	squamous cell carcinoma antigen recognized by T cells 3	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21447833
1323213	Sart3	squamous cell carcinoma antigen recognized by T cells 3	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21447833
1323213	Sart3	squamous cell carcinoma antigen recognized by T cells 3	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21447833
1323213	Sart3	squamous cell carcinoma antigen recognized by T cells 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1323213	Sart3	squamous cell carcinoma antigen recognized by T cells 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1323216	Ldah	lipid droplet associated hydrolase	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1323216	Ldah	lipid droplet associated hydrolase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:27836991
1323216	Ldah	lipid droplet associated hydrolase	gene	MP:0003212	increased susceptibility to age related obesity		IEA		N	RGD:5509061	20161103	MGI			
1323216	Ldah	lipid droplet associated hydrolase	gene	MP:0006325	impaired hearing		IEA		N	RGD:5509061	20161103	MGI			
1323216	Ldah	lipid droplet associated hydrolase	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IEA		N	RGD:5509061	20161103	MGI			
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0001841	decreased level of surface class I molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:19272190
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163195
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:19272190
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20181011	MGI			
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19272190
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19272190
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0010848	decreased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11163195
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0020943	increased susceptibility to Flaviviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:29746837
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0031040	increased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:19272190
1323218	Stat2	signal transducer and activator of transcription 2	gene	MP:0031044	increased susceptibility to Flaviviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:29746837
1323224	Vgll4	vestigial like family member 4	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0010605	thick pulmonary valve cusps		IAGP		N	RGD:5509061	20191010	MGI			PMID:30789911
1323224	Vgll4	vestigial like family member 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323224	Vgll4	vestigial like family member 4	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20220519	MGI			
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20260402	MGI			
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0004085	abnormal heartbeat		IEA		N	RGD:5509061	20220519	MGI			
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0006065	abnormal heart position or orientation		IEA		N	RGD:5509061	20220519	MGI			
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0010752	impaired mucociliary clearance		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0011248	visceral organ asymmetry		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0030049	prominent forehead		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323225	Lrrc56	leucine rich repeat containing 56	gene	MP:0030245	round head		IAGP		N	RGD:5509061	20260122	MGI			PMID:41477643
1323227	Arl15	ADP-ribosylation factor-like 15	gene	MP:0000757	herniated abdominal wall		IEA		N	RGD:5509061	20250508	MGI			
1323227	Arl15	ADP-ribosylation factor-like 15	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20211021	MGI			
1323227	Arl15	ADP-ribosylation factor-like 15	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20221215	MGI			
1323227	Arl15	ADP-ribosylation factor-like 15	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323229	Best1	bestrophin 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20191212	MGI			PMID:31201163
1323229	Best1	bestrophin 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20191212	MGI			PMID:31201163
1323229	Best1	bestrophin 1	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053664
1323229	Best1	bestrophin 1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053664
1323229	Best1	bestrophin 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16636205
1323229	Best1	bestrophin 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053664
1323229	Best1	bestrophin 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16636205
1323229	Best1	bestrophin 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20053664
1323229	Best1	bestrophin 1	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323229	Best1	bestrophin 1	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20160602	MGI			PMID:25941382
1323232	Pdcd1	programmed cell death 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1323232	Pdcd1	programmed cell death 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20200618	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1323232	Pdcd1	programmed cell death 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0001627	abnormal cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911591
1323232	Pdcd1	programmed cell death 1	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911591
1323232	Pdcd1	programmed cell death 1	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485649
1323232	Pdcd1	programmed cell death 1	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0002983	increased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19420345
1323232	Pdcd1	programmed cell death 1	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485649
1323232	Pdcd1	programmed cell death 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182110
1323232	Pdcd1	programmed cell death 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1323232	Pdcd1	programmed cell death 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1323232	Pdcd1	programmed cell death 1	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911591
1323232	Pdcd1	programmed cell death 1	gene	MP:0004752	decreased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1323232	Pdcd1	programmed cell death 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182110
1323232	Pdcd1	programmed cell death 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832734
1323232	Pdcd1	programmed cell death 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911591
1323232	Pdcd1	programmed cell death 1	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911591
1323232	Pdcd1	programmed cell death 1	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911591
1323232	Pdcd1	programmed cell death 1	gene	MP:0005000	abnormal immune tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911591
1323232	Pdcd1	programmed cell death 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911591
1323232	Pdcd1	programmed cell death 1	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1323232	Pdcd1	programmed cell death 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17911591
1323232	Pdcd1	programmed cell death 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1323232	Pdcd1	programmed cell death 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11209085
1323232	Pdcd1	programmed cell death 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182110
1323232	Pdcd1	programmed cell death 1	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0008091	decreased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20200618	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9796923
1323232	Pdcd1	programmed cell death 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1323232	Pdcd1	programmed cell death 1	gene	MP:0009148	pancreas necrosis		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0009646	urinary bladder inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1323232	Pdcd1	programmed cell death 1	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0010220	decreased T-helper 17 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949674
1323232	Pdcd1	programmed cell death 1	gene	MP:0010857	pulmonary necrosis		IAGP		N	RGD:5509061	20160602	MGI			PMID:25964334
1323232	Pdcd1	programmed cell death 1	gene	MP:0011887	decreased circulating lipase level		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0013295	pancreas atrophy		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0013772	increased effector memory T-helper cell number		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1323232	Pdcd1	programmed cell death 1	gene	MP:0020993	abnormal urine cytokine level		IAGP		N	RGD:5509061	20210408	MGI			PMID:22432050
1323232	Pdcd1	programmed cell death 1	gene	MP:0021160	decreased heart right ventricle wall thickness		IAGP		N	RGD:5509061	20231221	MGI			PMID:11209085
1323235	Get4	golgi to ER traffic protein 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323235	Get4	golgi to ER traffic protein 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21548880
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21548880
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21548880
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23141541
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23141541
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21548880
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0004203	abnormal cranial flexure morphology		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23141541
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23141541
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23141541
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23141541
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21548880
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190606	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:23141541
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:30532139
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1323236	Ttbk2	tau tubulin kinase 2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210826	MGI			
1323238	Fam3b	FAM3 metabolism regulating signaling molecule B	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1323238	Fam3b	FAM3 metabolism regulating signaling molecule B	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566664
1323238	Fam3b	FAM3 metabolism regulating signaling molecule B	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566664
1323238	Fam3b	FAM3 metabolism regulating signaling molecule B	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566664
1323238	Fam3b	FAM3 metabolism regulating signaling molecule B	gene	MP:0003839	abnormal insulin clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566664
1323238	Fam3b	FAM3 metabolism regulating signaling molecule B	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566664
1323242	Ankrd50	ankyrin repeat domain 50	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1323242	Ankrd50	ankyrin repeat domain 50	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230601	MGI			
1323242	Ankrd50	ankyrin repeat domain 50	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1323245	Nkapl	NFKB activating protein-like	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20160512	MGI			PMID:25875095
1323245	Nkapl	NFKB activating protein-like	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160512	MGI			PMID:25875095
1323245	Nkapl	NFKB activating protein-like	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20160512	MGI			PMID:25875095
1323245	Nkapl	NFKB activating protein-like	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20160512	MGI			PMID:25875095
1323245	Nkapl	NFKB activating protein-like	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20160512	MGI			PMID:25875095
1323247	F13b	coagulation factor XIII, beta subunit	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20150827	MGI			PMID:18224415
1323249	Thoc3	THO complex 3	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20240926	MGI			
1323249	Thoc3	THO complex 3	gene	MP:0002718	abnormal inner cell mass morphology		IEA		N	RGD:5509061	20240926	MGI			
1323249	Thoc3	THO complex 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220519	MGI			
1323249	Thoc3	THO complex 3	gene	MP:0005028	abnormal trophectoderm morphology		IEA		N	RGD:5509061	20240926	MGI			
1323249	Thoc3	THO complex 3	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1323249	Thoc3	THO complex 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1323249	Thoc3	THO complex 3	gene	MP:0012111	failure of morula compaction		IEA		N	RGD:5509061	20240926	MGI			
1323249	Thoc3	THO complex 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1323249	Thoc3	THO complex 3	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:19718027
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20171005	MGI			PMID:19718027
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393260
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20171005	MGI			PMID:19718027
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20171005	MGI			PMID:19718027
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:19718027
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20171005	MGI			PMID:19718027
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20160804	MGI			
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393260
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150430	MGI			PMID:25038042
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20171005	MGI			PMID:19718027
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20171005	MGI			PMID:19718027
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20171005	MGI			PMID:19718027
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573616
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0012156	rostral-caudal axis duplication		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0012181	increased somite number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0012274	increased axial mesoderm size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668413
1323252	Tcf7l1	transcription factor 7 like 1 (T cell specific, HMG box)	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:22573616
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323256	Pilrb1	paired immunoglobin-like type 2 receptor beta 1	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065029
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160714	MGI			PMID:24583640
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160623	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20160623	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20160623	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20160623	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20160623	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20160623	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20160623	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20160714	MGI			PMID:24583640
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20160623	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20160714	MGI			PMID:24583640
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009303	decreased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20160623	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20160714	MGI			PMID:24583640
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0010046	decreased omental fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20160714	MGI			PMID:24583640
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0011581	increased triglyceride lipase activity		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20160728	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0014605	dark liver		IAGP		N	RGD:5509061	20250206	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20180125	MGI			PMID:24556704
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20180125	MGI			PMID:25381555
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:24194501
1323257	G0s2	G0/G1 switch gene 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:25381555
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0002453	abnormal B lymphocyte antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0005040	abnormal MHC II cell surface expression on macrophages		IAGP		N	RGD:5509061	20141003	MGI			PMID:10621974
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0005040	abnormal MHC II cell surface expression on macrophages		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323260	Rfx5	regulatory factor X, 5 (influences HLA class II expression)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323265	Tifab	TRAF-interacting protein with forkhead-associated domain, family member B	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20160804	MGI			
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20160804	MGI			
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:24923387
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160407	MGI			PMID:24923387
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:24923387
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:24923387
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:24923387
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:24923387
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160804	MGI			
1323268	Rhobtb3	Rho-related BTB domain containing 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160407	MGI			PMID:24923387
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0001460	abnormal olfactory discrimination memory		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0003110	absent malleus processus brevis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0008377	absent malleus manubrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0008382	gonial bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0009879	abnormal arcus anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0009943	abnormal olfactory bulb periglomerular cell morphology		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0009949	abnormal olfactory bulb granule cell layer morphology		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0010371	abnormal epiglottis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0010994	aerophagia		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141106	MGI			PMID:24487590
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0012284	increased sternebra number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17586487
1323270	Tshz1	teashirt zinc finger family member 1	gene	MP:0030291	short soft palate		IAGP		N	RGD:5509061	20171102	MGI			PMID:17586487
1323272	Nid2	nidogen 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26683663
1323272	Nid2	nidogen 2	gene	MP:0003200	calcified joint		IAGP		N	RGD:5509061	20160811	MGI			PMID:26683663
1323272	Nid2	nidogen 2	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20160811	MGI			PMID:26683663
1323272	Nid2	nidogen 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17008882
1323272	Nid2	nidogen 2	gene	MP:0006429	abnormal hyaline cartilage morphology		IAGP		N	RGD:5509061	20160811	MGI			PMID:26683663
1323274	Bpifc	BPI fold containing family C	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20220811	MGI			
1323274	Bpifc	BPI fold containing family C	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1323274	Bpifc	BPI fold containing family C	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20221215	MGI			
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:19365570
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20260402	MGI			
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19365570
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20220811	MGI			
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20220519	MGI			
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19365570
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210826	MGI			
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0004222	iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19365570
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0005195	abnormal posterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19365570
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19365570
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19365570
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19365570
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19365570
1323277	Bcar3	breast cancer anti-estrogen resistance 3	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:19365570
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20190808	MGI			
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20210520	MGI			
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20201029	MGI			PMID:28436964
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190808	MGI			
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0004882	enlarged lung		IEA		N	RGD:5509061	20210520	MGI			
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20201029	MGI			PMID:28436964
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0004917	abnormal T cell selection		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20201029	MGI			PMID:28436964
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20201029	MGI			PMID:28436964
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20201029	MGI			PMID:28436964
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:28436964
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:28436964
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:28436964
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20201029	MGI			PMID:28436964
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0010134	decreased DN3 thymocyte number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0013592	small thymus cortex		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0013741	absent thymus corticomedullary boundary		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323280	Lrrc8a	leucine rich repeat containing 8A VRAC subunit A	gene	MP:0014180	abnormal thymus apoptosis		IAGP		N	RGD:5509061	20170314	MGI			PMID:24752297
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0003130	anal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0009576	oral atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0009576	oral atresia		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0009884	palatal shelf fusion with tongue or mandible		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20170309	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0011771	abnormal genital tubercle morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0013530	abnormal periderm morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0013531	abnormal periderm development		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:12194825
1323282	Ripk4	receptor-interacting serine-threonine kinase 4	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:25430793
1323285	Plscr4	phospholipid scramblase 4	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20260402	MGI			
1323285	Plscr4	phospholipid scramblase 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1323285	Plscr4	phospholipid scramblase 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1323285	Plscr4	phospholipid scramblase 4	gene	MP:0001192	scaly skin		IEA		N	RGD:5509061	20260402	MGI			
1323285	Plscr4	phospholipid scramblase 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1323285	Plscr4	phospholipid scramblase 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1323285	Plscr4	phospholipid scramblase 4	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20260402	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20181227	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170105	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20160811	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20201231	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20201231	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20160811	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20201231	MGI			
1323293	Dpf2	double PHD fingers 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1323295	Smtnl1	smoothelin-like 1	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18310078
1323295	Smtnl1	smoothelin-like 1	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18310078
1323295	Smtnl1	smoothelin-like 1	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18310078
1323295	Smtnl1	smoothelin-like 1	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18310078
1323295	Smtnl1	smoothelin-like 1	gene	MP:0012107	enhanced exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18310078
1323297	Uba5	ubiquitin-like modifier activating enzyme 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20018847
1323303	Hdac11	histone deacetylase 11	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1323303	Hdac11	histone deacetylase 11	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20160225	MGI			PMID:25155994
1323303	Hdac11	histone deacetylase 11	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20160225	MGI			PMID:25155994
1323303	Hdac11	histone deacetylase 11	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20160225	MGI			PMID:24747960
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209306
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0009277	increased brain tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17925231
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117986
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17938250
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323305	Bub1	BUB1, mitotic checkpoint serine/threonine kinase	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17938250
1323312	Itga11	integrin alpha 11	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20201231	MGI			
1323312	Itga11	integrin alpha 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0003053	delayed tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0004830	short incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1323312	Itga11	integrin alpha 11	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20200514	MGI			
1323312	Itga11	integrin alpha 11	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0030460	enamel pits		IAGP		N	RGD:5509061	20171221	MGI			PMID:17420280
1323312	Itga11	integrin alpha 11	gene	MP:0030509	increased number of epithelial cell rests of Malassez		IAGP		N	RGD:5509061	20180111	MGI			PMID:17420280
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20160811	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20170105	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20201022	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20200402	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210826	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001454	abnormal cued conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001469	abnormal contextual conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20201022	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20200402	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160421	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0011906	increased Schwann cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:16136673
1323314	Nab2	Ngfi-A binding protein 2	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20210128	MGI			
1323317	Rsrc2	arginine/serine-rich coiled-coil 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1323320	Ubap2	ubiquitin-associated protein 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1323320	Ubap2	ubiquitin-associated protein 2	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20220519	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13989207
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0000400	abnormal awl hair morphology		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0000402	abnormal zigzag hair morphology		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0000414	alopecia		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748961
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0000422	delayed hair appearance		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0000424	retarded hair growth		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001270	distended abdomen		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001282	short vibrissae		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748961
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001575	cyanosis		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19429912
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748961
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19429912
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931657
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19429912
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931657
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19429912
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11094083
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19429912
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748961
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19429912
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201231	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:11094083
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20201022	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19429912
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0006363	absent auchene hairs		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0008538	decreased zigzag hair amount		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:19429912
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0009003	abnormal vibrissa number		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20150730	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011086	postnatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748961
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011088	neonatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011090	perinatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011092	embryonic lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18931657
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19429912
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748961
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0011748	intestinal fibrosis		IEA		N	RGD:5509061	20150730	MGI			
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748961
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20150730	MGI			PMID:291594
1323322	Sox18	SRY (sex determining region Y)-box 18	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1323326	Sec24d	SEC24 homolog D, COPII coat complex component	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20200514	MGI			
1323326	Sec24d	SEC24 homolog D, COPII coat complex component	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20200514	MGI			
1323326	Sec24d	SEC24 homolog D, COPII coat complex component	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170518	MGI			PMID:24876386
1323326	Sec24d	SEC24 homolog D, COPII coat complex component	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20200514	MGI			
1323326	Sec24d	SEC24 homolog D, COPII coat complex component	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23596517
1323326	Sec24d	SEC24 homolog D, COPII coat complex component	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23596517
1323326	Sec24d	SEC24 homolog D, COPII coat complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200416	MGI			PMID:29326438
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20200416	MGI			PMID:29326438
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0001884	mammary gland alveolar hyperplasia		IAGP		N	RGD:5509061	20200416	MGI			PMID:29326438
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0001885	mammary gland duct hyperplasia		IAGP		N	RGD:5509061	20200416	MGI			PMID:29326438
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200416	MGI			PMID:29326438
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20200416	MGI			PMID:29326438
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20211021	MGI			PMID:29038465
1323328	Nmi	N-myc (and STAT) interactor	gene	MP:0013782	abnormal mammary duct terminal end bud morphology		IAGP		N	RGD:5509061	20200416	MGI			PMID:29326438
1323329	Cep295	centrosomal protein 295	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20240523	MGI			
1323329	Cep295	centrosomal protein 295	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20240523	MGI			
1323329	Cep295	centrosomal protein 295	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1323329	Cep295	centrosomal protein 295	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1323331	Capg	capping actin protein, gelsolin like	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514591
1323331	Capg	capping actin protein, gelsolin like	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573680
1323331	Capg	capping actin protein, gelsolin like	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573680
1323331	Capg	capping actin protein, gelsolin like	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573680
1323331	Capg	capping actin protein, gelsolin like	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514591
1323331	Capg	capping actin protein, gelsolin like	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14573680
1323333	Fgd3	FYVE, RhoGEF and PH domain containing 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1323333	Fgd3	FYVE, RhoGEF and PH domain containing 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1323333	Fgd3	FYVE, RhoGEF and PH domain containing 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1323333	Fgd3	FYVE, RhoGEF and PH domain containing 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1323333	Fgd3	FYVE, RhoGEF and PH domain containing 3	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1323333	Fgd3	FYVE, RhoGEF and PH domain containing 3	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1323333	Fgd3	FYVE, RhoGEF and PH domain containing 3	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220519	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000215	absent erythrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000216	absent erythroid progenitor cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:24711581
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20181227	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24711581
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24711581
1323335	Gfi1b	growth factor independent 1B	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17095621
1323335	Gfi1b	growth factor independent 1B	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24711581
1323335	Gfi1b	growth factor independent 1B	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24711581
1323335	Gfi1b	growth factor independent 1B	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826720
1323335	Gfi1b	growth factor independent 1B	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:24711581
1323335	Gfi1b	growth factor independent 1B	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826720
1323335	Gfi1b	growth factor independent 1B	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826720
1323335	Gfi1b	growth factor independent 1B	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24711581
1323335	Gfi1b	growth factor independent 1B	gene	MP:0003714	absent platelets		IAGP		N	RGD:5509061	20141003	MGI			PMID:24711581
1323335	Gfi1b	growth factor independent 1B	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0004229	abnormal embryonic erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0004230	abnormal embryonic erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826720
1323335	Gfi1b	growth factor independent 1B	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826720
1323335	Gfi1b	growth factor independent 1B	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826720
1323335	Gfi1b	growth factor independent 1B	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20826720
1323335	Gfi1b	growth factor independent 1B	gene	MP:0010896	decreased lung compliance		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20250508	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24711581
1323335	Gfi1b	growth factor independent 1B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17095621
1323335	Gfi1b	growth factor independent 1B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323335	Gfi1b	growth factor independent 1B	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260611	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:11825872
1323335	Gfi1b	growth factor independent 1B	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:17095621
1323340	Gstm6	glutathione S-transferase, mu 6	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20260402	MGI			
1323340	Gstm6	glutathione S-transferase, mu 6	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1323340	Gstm6	glutathione S-transferase, mu 6	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1323340	Gstm6	glutathione S-transferase, mu 6	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128702
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24069363
1323343	Fxr1	FMR1 autosomal homolog 1	gene	MP:0014273	abnormal skin vasculature morphology		IAGP		N	RGD:5509061	20230810	MGI			PMID:15128702
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20151203	MGI			PMID:24276541
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151203	MGI			PMID:24276541
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001376	abnormal mating receptivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20250206	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20151203	MGI			PMID:24276541
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:24276541
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20151203	MGI			PMID:24276541
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0008295	abnormal adrenal gland zona reticularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962384
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0009137	decreased brown fat lipid droplet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0009396	small endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:14651970
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:17143286
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0031286	unilateral cryptorchism		IAGP		N	RGD:5509061	20211014	MGI			PMID:11483573
1323346	Arid5b	AT-rich interaction domain 5B	gene	MP:0031287	bilateral cryptorchism		IAGP		N	RGD:5509061	20211014	MGI			PMID:11483573
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20181227	MGI			
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8977324
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713566
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8977324
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238890
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713566
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713566
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238890
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002491	decreased IgD level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20210128	MGI			
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238890
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713566
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568779
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8977324
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568779
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568779
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16713566
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568779
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568779
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238890
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238890
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574333
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:8977324
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8977324
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8977324
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8977324
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8977324
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008523	absent lymph node germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:8849728
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568779
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568779
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568779
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17568779
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11238890
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1323348	Pou2af1	POU domain, class 2, associating factor 1	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210128	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20190502	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0012128	abnormal blastocyst formation		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1323350	Rbbp4	retinoblastoma binding protein 4, chromatin remodeling factor	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20240627	MGI			PMID:32285100
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0010666	abnormal vitelline vein morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323356	Cd2bp2	CD2 cytoplasmic tail binding protein 2	gene	MP:0012131	small visceral yolk sac		IAGP		N	RGD:5509061	20200310	MGI			PMID:26082520
1323357	Spata24	spermatogenesis associated 24	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1323357	Spata24	spermatogenesis associated 24	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1323357	Spata24	spermatogenesis associated 24	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1323357	Spata24	spermatogenesis associated 24	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20201022	MGI			PMID:32588039
1323361	1110059G10Rik	RIKEN cDNA 1110059G10 gene	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20150430	MGI			
1323364	Hpf1	histone PARylation factor 1	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20181227	MGI			
1323364	Hpf1	histone PARylation factor 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1323366	Tcerg1	transcription elongation regulator 1 (CA150)	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1323366	Tcerg1	transcription elongation regulator 1 (CA150)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20171102	MGI			PMID:25569111
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20250213	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0003085	abnormal egg cylinder morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:25569111
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20171102	MGI			PMID:25569111
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20210128	MGI			PMID:32943573
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0014619	absent spermatogonia		IAGP		N	RGD:5509061	20250213	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0014631	abnormal elongated spermatid morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0020421	increased freezing behavior		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0020845	abnormal DNA-templated transcription		IAGP		N	RGD:5509061	20260702	MGI			PMID:41842966
1323368	Mettl3	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	gene	MP:0031739	impaired translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:28914256
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21089073
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001068	abnormal mandibular nerve branching		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001075	abnormal accessory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:34767447
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:36693621
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003679	ear lobe hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1323369	Mesp1	mesoderm posterior 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578861
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004032	abnormal interventricular groove morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004420	parietal bone hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004555	pharynx hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004569	glossopharyngeal nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:16996494
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578861
1323369	Mesp1	mesoderm posterior 1	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1323369	Mesp1	mesoderm posterior 1	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1323369	Mesp1	mesoderm posterior 1	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0009490	abnormal heart left atrium auricular region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21089073
1323369	Mesp1	mesoderm posterior 1	gene	MP:0009912	decreased hyoid bone size		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18440989
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010422	heart right ventricle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21089073
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010422	heart right ventricle hypoplasia		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010433	double inlet heart left ventricle		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010453	abnormal coronary vein morphology		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010455	aortopulmonary window		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010503	myocardial trabeculae hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18547789
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010527	bicuspid pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20171109	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010643	absent fourth pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0010644	absent sixth pharyngeal arch		IAGP		N	RGD:5509061	20171109	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578861
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160721	MGI			PMID:26932671
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:24748541
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11578861
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20230713	MGI			PMID:26102480
1323369	Mesp1	mesoderm posterior 1	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9739106
1323369	Mesp1	mesoderm posterior 1	gene	MP:0012184	absent paraxial mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10887078
1323369	Mesp1	mesoderm posterior 1	gene	MP:0012278	abnormal cardiogenic mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10393122
1323369	Mesp1	mesoderm posterior 1	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0013265	abnormal fourth pharyngeal pouch morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0013268	second pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0013268	second pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0013269	third pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1323369	Mesp1	mesoderm posterior 1	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:16554359
1323369	Mesp1	mesoderm posterior 1	gene	MP:0030084	tympanic ring hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323369	Mesp1	mesoderm posterior 1	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1323369	Mesp1	mesoderm posterior 1	gene	MP:0030334	absent sixth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0030335	absent third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0030340	absent fourth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:16914493
1323369	Mesp1	mesoderm posterior 1	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1323370	Dimt1	DIM1 rRNA methyltransferase and ribosome maturation factor	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20250508	MGI			
1323370	Dimt1	DIM1 rRNA methyltransferase and ribosome maturation factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141003	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323373	Prc1	protein regulator of cytokinesis 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20260402	MGI			
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20220310	MGI			PMID:33408128
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20220310	MGI			PMID:33408128
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20220310	MGI			PMID:33408128
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20220310	MGI			PMID:33408128
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20220310	MGI			PMID:33408128
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20220310	MGI			PMID:33408128
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230601	MGI			
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230601	MGI			
1323375	Ctdp1	CTD phosphatase subunit 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20220310	MGI			PMID:33408128
1323377	Dglucy	D-glutamate cyclase	gene	MP:0030736	increased glutamic acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:28266638
1323379	Rgp1	RAB6A GEF compex partner 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1323379	Rgp1	RAB6A GEF compex partner 1	gene	MP:0000955	abnormal spinal cord morphology		IEA		N	RGD:5509061	20210826	MGI			
1323379	Rgp1	RAB6A GEF compex partner 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1323379	Rgp1	RAB6A GEF compex partner 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1323379	Rgp1	RAB6A GEF compex partner 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1323379	Rgp1	RAB6A GEF compex partner 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323379	Rgp1	RAB6A GEF compex partner 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323379	Rgp1	RAB6A GEF compex partner 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1323379	Rgp1	RAB6A GEF compex partner 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1323381	Ddx41	DEAD box helicase 41	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1323381	Ddx41	DEAD box helicase 41	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1323381	Ddx41	DEAD box helicase 41	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323381	Ddx41	DEAD box helicase 41	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1323381	Ddx41	DEAD box helicase 41	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:29871919
1323385	Rragc	Ras-related GTP binding C	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0008806	increased circulating amylase level		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0010282	decreased organ/body region tumor incidence		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0014433	increased cytokine level		IAGP		N	RGD:5509061	20260305	MGI			PMID:38849535
1323385	Rragc	Ras-related GTP binding C	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323385	Rragc	Ras-related GTP binding C	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20230601	MGI			PMID:34260908
1323389	Arrdc4	arrestin domain containing 4	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1323389	Arrdc4	arrestin domain containing 4	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1323389	Arrdc4	arrestin domain containing 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20161208	MGI			PMID:27462458
1323389	Arrdc4	arrestin domain containing 4	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20220519	MGI			
1323389	Arrdc4	arrestin domain containing 4	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20231207	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733990
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20231207	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733990
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987638
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987638
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190516	MGI			PMID:28790031
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19737919
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733990
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002208	abnormal germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19737919
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17000121
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002747	abnormal aortic valve morphology		IEA		N	RGD:5509061	20141003	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0002982	abnormal primordial germ cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937476
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733990
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20141003	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987638
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19737919
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19737919
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0004898	uterine hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987638
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19737919
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0005327	abnormal mesangial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0006339	abnormal third pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008093	abnormal memory B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008100	absent plasma cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733990
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15937476
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19737919
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008393	absent primordial germ cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563324
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20160505	MGI			PMID:21156282
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22987638
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20190516	MGI			PMID:28790031
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20190516	MGI			PMID:28790031
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20715164
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0010188	abnormal T follicular helper cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21948081
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20141003	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0010488	abnormal left subclavian artery morphology		IEA		N	RGD:5509061	20141003	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19737919
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15492122
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22733990
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19737919
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0011262	abnormal pharyngeal arch mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15750184
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20231207	MGI			
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:19737919
1323392	Prdm1	PR domain containing 1, with ZNF domain	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:19664942
1323396	Dtx4	deltex 4, E3 ubiquitin ligase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20200514	MGI			
1323396	Dtx4	deltex 4, E3 ubiquitin ligase	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20200514	MGI			
1323396	Dtx4	deltex 4, E3 ubiquitin ligase	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20200514	MGI			
1323396	Dtx4	deltex 4, E3 ubiquitin ligase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20200514	MGI			
1323396	Dtx4	deltex 4, E3 ubiquitin ligase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1323396	Dtx4	deltex 4, E3 ubiquitin ligase	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220519	MGI			
1323396	Dtx4	deltex 4, E3 ubiquitin ligase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1323407	Nt5el	5' nucleotidase, ecto-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1323412	Tpcn2	two pore segment channel 2	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20230420	MGI			PMID:36641477
1323412	Tpcn2	two pore segment channel 2	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20201022	MGI			
1323412	Tpcn2	two pore segment channel 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26769314
1323412	Tpcn2	two pore segment channel 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063126
1323412	Tpcn2	two pore segment channel 2	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20230420	MGI			PMID:36641477
1323412	Tpcn2	two pore segment channel 2	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19387438
1323412	Tpcn2	two pore segment channel 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1323412	Tpcn2	two pore segment channel 2	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20230420	MGI			PMID:36641477
1323412	Tpcn2	two pore segment channel 2	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20230420	MGI			PMID:36641477
1323412	Tpcn2	two pore segment channel 2	gene	MP:0005391	vision/eye phenotype		IAGP		N	RGD:5509061	20230420	MGI			PMID:36641477
1323412	Tpcn2	two pore segment channel 2	gene	MP:0010190	abnormal retina melanocyte morphology		IAGP		N	RGD:5509061	20230420	MGI			PMID:36641477
1323412	Tpcn2	two pore segment channel 2	gene	MP:0011277	decreased tail pigmentation		IAGP		N	RGD:5509061	20230420	MGI			PMID:36641477
1323413	Mrm1	mitochondrial rRNA methyltransferase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323415	Casp14	caspase 14	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1323415	Casp14	caspase 14	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1323415	Casp14	caspase 14	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1323415	Casp14	caspase 14	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515931
1323415	Casp14	caspase 14	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515931
1323415	Casp14	caspase 14	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515931
1323415	Casp14	caspase 14	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156206
1323415	Casp14	caspase 14	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515931
1323415	Casp14	caspase 14	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1323415	Casp14	caspase 14	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17515931
1323415	Casp14	caspase 14	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20210128	MGI			
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24497849
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21179166
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21179166
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21179166
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20210415	MGI			PMID:29967452
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21179166
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20150205	MGI			PMID:24497849
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20211021	MGI			
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0004130	abnormal muscle cell glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20150205	MGI			PMID:24497849
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141160
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005068	abnormal NK cell morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:29967452
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20150205	MGI			PMID:24497849
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0006420	abnormal peritubular myoid cell morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0006428	ectopic Sertoli cells		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20210415	MGI			PMID:29967452
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22504639
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22504639
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0009131	decreased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22504639
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046571
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141160
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141160
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160304	MGI			PMID:22504639
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0020355	abnormal Sertoli cell barrier morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323418	Rptor	regulatory associated protein of MTOR, complex 1	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:29961810
1323419	Foxred1	FAD-dependent oxidoreductase domain containing 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1323419	Foxred1	FAD-dependent oxidoreductase domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323419	Foxred1	FAD-dependent oxidoreductase domain containing 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323428	Arpc5	actin related protein 2/3 complex, subunit 5	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20230831	MGI			PMID:37382373
1323428	Arpc5	actin related protein 2/3 complex, subunit 5	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20230831	MGI			PMID:37382373
1323428	Arpc5	actin related protein 2/3 complex, subunit 5	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20230831	MGI			PMID:37382373
1323428	Arpc5	actin related protein 2/3 complex, subunit 5	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20230831	MGI			PMID:37382373
1323428	Arpc5	actin related protein 2/3 complex, subunit 5	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20230831	MGI			PMID:37382373
1323428	Arpc5	actin related protein 2/3 complex, subunit 5	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20230831	MGI			PMID:37382373
1323428	Arpc5	actin related protein 2/3 complex, subunit 5	gene	MP:0014044	absent cardiac outflow tract		IAGP		N	RGD:5509061	20230831	MGI			PMID:37382373
1323430	Pidd1	p53 induced death domain protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19364921
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20260402	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20210826	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20221215	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20210826	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210520	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210826	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210520	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1323435	Zfp280d	zinc finger protein 280D	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210520	MGI			
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16597604
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102581
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0001939	secondary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0001939	secondary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102581
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0002534	abnormal type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371360
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102581
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0002996	ovotestis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102581
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371360
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16597604
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0006424	absent testis cords		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102581
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287712
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371360
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23102580
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691480
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20180118	MGI			PMID:25071184
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20180118	MGI			PMID:25071184
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20180118	MGI			PMID:25071184
1323437	Gadd45g	growth arrest and DNA-damage-inducible 45 gamma	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:16287712
1323440	Ddx55	DEAD box helicase 55	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201022	MGI			
1323440	Ddx55	DEAD box helicase 55	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1323440	Ddx55	DEAD box helicase 55	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323442	Fermt2	fermitin family member 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0000075	absent neurocranium		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483218
1323442	Fermt2	fermitin family member 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483218
1323442	Fermt2	fermitin family member 2	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0004338	small clavicle		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0004626	vertebral compression		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18174465
1323442	Fermt2	fermitin family member 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483218
1323442	Fermt2	fermitin family member 2	gene	MP:0012279	wide sternum		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20160929	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20160922	MGI			PMID:26151572
1323442	Fermt2	fermitin family member 2	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:18483218
1323443	Stbd1	starch binding domain 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1323443	Stbd1	starch binding domain 1	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20211028	MGI			PMID:27358407
1323443	Stbd1	starch binding domain 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20211028	MGI			PMID:27358407
1323443	Stbd1	starch binding domain 1	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20211028	MGI			PMID:27358407
1323445	Syngr3	synaptogyrin 3	gene	MP:0002064	seizures		IEA		N	RGD:5509061	20150219	MGI			
1323445	Syngr3	synaptogyrin 3	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20241121	MGI			
1323445	Syngr3	synaptogyrin 3	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:33472038
1323445	Syngr3	synaptogyrin 3	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:33472038
1323445	Syngr3	synaptogyrin 3	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20241121	MGI			
1323445	Syngr3	synaptogyrin 3	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20241121	MGI			
1323452	Hspa9	heat shock protein family A (Hsp70) member 9	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25550197
1323452	Hspa9	heat shock protein family A (Hsp70) member 9	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160225	MGI			PMID:25550197
1323456	Tpgs1	tubulin polyglutamylase complex subunit 1	gene	MP:0001355	submission towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242242
1323456	Tpgs1	tubulin polyglutamylase complex subunit 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242242
1323456	Tpgs1	tubulin polyglutamylase complex subunit 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242242
1323456	Tpgs1	tubulin polyglutamylase complex subunit 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242242
1323456	Tpgs1	tubulin polyglutamylase complex subunit 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242242
1323456	Tpgs1	tubulin polyglutamylase complex subunit 1	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242242
1323456	Tpgs1	tubulin polyglutamylase complex subunit 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242242
1323456	Tpgs1	tubulin polyglutamylase complex subunit 1	gene	MP:0031352	absent sperm axonemal central pair		IAGP		N	RGD:5509061	20220811	MGI			PMID:12242242
1323459	Mab21l2	mab-21-like 2	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20260402	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20230601	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20220519	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20231207	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0009725	absent lens vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385160
1323459	Mab21l2	mab-21-like 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1323459	Mab21l2	mab-21-like 2	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1323461	Ccrl2	C-C motif chemokine receptor-like 2	gene	MP:0002148	abnormal hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606167
1323461	Ccrl2	C-C motif chemokine receptor-like 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1323461	Ccrl2	C-C motif chemokine receptor-like 2	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606167
1323461	Ccrl2	C-C motif chemokine receptor-like 2	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794339
1323461	Ccrl2	C-C motif chemokine receptor-like 2	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606167
1323461	Ccrl2	C-C motif chemokine receptor-like 2	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606167
1323461	Ccrl2	C-C motif chemokine receptor-like 2	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606167
1323461	Ccrl2	C-C motif chemokine receptor-like 2	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606167
1323461	Ccrl2	C-C motif chemokine receptor-like 2	gene	MP:0010740	abnormal dendritic cell chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606167
1323463	Ferd3l	Fer3 like bHLH transcription factor	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460368
1323463	Ferd3l	Fer3 like bHLH transcription factor	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460368
1323463	Ferd3l	Fer3 like bHLH transcription factor	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460368
1323463	Ferd3l	Fer3 like bHLH transcription factor	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460368
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20241121	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0012507	midbrain atrophy		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0030003	hippocampus atrophy		IAGP		N	RGD:5509061	20201105	MGI			PMID:30333725
1323466	Eef1d	eukaryotic translation elongation factor 1 delta	gene	MP:0031740	enhanced translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:30333725
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20200514	MGI			
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20200514	MGI			
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20211021	MGI			
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210826	MGI			
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323467	Ddi2	DNA-damage inducible protein 2	gene	MP:0031661	prenatal lethality prior to heart atrial septation, complete penetrance		IAGP		N	RGD:5509061	20250814	MGI			PMID:39328932
1323469	Polr3d	polymerase (RNA) III (DNA directed) polypeptide D	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1323469	Polr3d	polymerase (RNA) III (DNA directed) polypeptide D	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1323469	Polr3d	polymerase (RNA) III (DNA directed) polypeptide D	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20211021	MGI			
1323469	Polr3d	polymerase (RNA) III (DNA directed) polypeptide D	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20220519	MGI			
1323469	Polr3d	polymerase (RNA) III (DNA directed) polypeptide D	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201022	MGI			
1323469	Polr3d	polymerase (RNA) III (DNA directed) polypeptide D	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1323469	Polr3d	polymerase (RNA) III (DNA directed) polypeptide D	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4853271
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:672986
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:12470976
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:23631845
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:4853271
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0001309	hydropic eye lens fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:4853271
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0002642	anisocytosis		IEA		N	RGD:5509061	20221201	MGI			
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4853271
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221201	MGI			
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0005654	porphyria		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0011890	increased circulating ferritin level		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323471	Cpox	coproporphyrinogen oxidase	gene	MP:0013165	absent forelimb buds		IAGP		N	RGD:5509061	20180628	MGI			PMID:28600349
1323475	Pop5	processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae)	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20240926	MGI			
1323475	Pop5	processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae)	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1323475	Pop5	processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1323475	Pop5	processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae)	gene	MP:0012111	failure of morula compaction		IEA		N	RGD:5509061	20240926	MGI			
1323475	Pop5	processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae)	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20240926	MGI			
1323475	Pop5	processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1323477	Rasal1	RAS protein activator like 1 (GAP1 like)	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20210729	MGI			PMID:30158531
1323479	Dtd1	D-tyrosyl-tRNA deacylase 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1323480	Gstcd	glutathione S-transferase, C-terminal domain containing	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20190502	MGI			
1323480	Gstcd	glutathione S-transferase, C-terminal domain containing	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20191128	MGI			PMID:31513609
1323480	Gstcd	glutathione S-transferase, C-terminal domain containing	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20201022	MGI			
1323480	Gstcd	glutathione S-transferase, C-terminal domain containing	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1323480	Gstcd	glutathione S-transferase, C-terminal domain containing	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20191128	MGI			PMID:31513609
1323481	Prss37	serine protease 37	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23553430
1323481	Prss37	serine protease 37	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23553430
1323481	Prss37	serine protease 37	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20220303	MGI			PMID:23553430
1323481	Prss37	serine protease 37	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220303	MGI			PMID:23553430
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000743	muscle spasm		IEA		N	RGD:5509061	20141003	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436707
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20180621	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20240801	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000749	muscle degeneration		IEA		N	RGD:5509061	20141003	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416502
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0000955	abnormal spinal cord morphology		IEA		N	RGD:5509061	20141003	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180621	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180621	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20240801	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180621	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368914
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20141003	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368914
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20111116	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20240801	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180621	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0002916	increased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:18771733
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368914
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18771733
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0002922	decreased post-tetanic potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368914
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889334
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0003225	axonal dystrophy		IEA		N	RGD:5509061	20141003	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0003415	priapism		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368914
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10889334
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0004166	abnormal limbic system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0004708	short lumbar vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368914
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0005277	abnormal brainstem morphology		IEA		N	RGD:5509061	20141003	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12368914
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0008222	decreased hippocampal commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0008232	abnormal cingulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416502
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0009434	paraparesis		IEA		N	RGD:5509061	20141003	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416502
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180621	MGI			PMID:24358326
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0020560	abnormal pontine nuclei morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:5855800
1323484	Usp14	ubiquitin specific peptidase 14	gene	MP:0020955	increased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20211230	MGI			PMID:24358326
1323486	Rcan3	regulator of calcineurin 3	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20250508	MGI			
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0003080	increased natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323488	Rhbdd3	rhomboid domain containing 3	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610400
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926766
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926766
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:7926766
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:7926766
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926766
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926766
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926766
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7926766
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0011286	decreased circulating erythropoietin level		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0012306	enhanced spatial learning		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0013660	abnormal bone marrow hematopoietic cell morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:33481887
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0020421	increased freezing behavior		IAGP		N	RGD:5509061	20170720	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28604739
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0031051	lymph node hemorrhage		IAGP		N	RGD:5509061	20200618	MGI			PMID:17577922
1323494	Lrfn2	leucine rich repeat and fibronectin type III domain containing 2	gene	MP:0031052	lymph node necrosis		IAGP		N	RGD:5509061	20200618	MGI			PMID:17577922
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0001819	abnormal immune cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665078
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20170105	MGI			
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665078
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234222
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20170105	MGI			
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24221084
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234222
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0008656	abnormal interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24447140
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:24221084
1323496	Gpr65	G-protein coupled receptor 65	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:24221084
1323498	Pals2	protein associated with LIN7 2, MAGUK family member	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20220519	MGI			
1323498	Pals2	protein associated with LIN7 2, MAGUK family member	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1323498	Pals2	protein associated with LIN7 2, MAGUK family member	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220519	MGI			
1323498	Pals2	protein associated with LIN7 2, MAGUK family member	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20220519	MGI			
1323498	Pals2	protein associated with LIN7 2, MAGUK family member	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220519	MGI			
1323498	Pals2	protein associated with LIN7 2, MAGUK family member	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20220519	MGI			
1323498	Pals2	protein associated with LIN7 2, MAGUK family member	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1323498	Pals2	protein associated with LIN7 2, MAGUK family member	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220519	MGI			
1323504	Zpr1	ZPR1 zinc finger	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767679
1323504	Zpr1	ZPR1 zinc finger	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767679
1323504	Zpr1	ZPR1 zinc finger	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767679
1323504	Zpr1	ZPR1 zinc finger	gene	MP:0008888	abnormal Cajal body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767679
1323504	Zpr1	ZPR1 zinc finger	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767679
1323504	Zpr1	ZPR1 zinc finger	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767679
1323504	Zpr1	ZPR1 zinc finger	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15767679
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0000879	increased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001063	abnormal trochlear nerve morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0004612	fusion of vertebral bodies		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0010008	abnormal Purkinje cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0013551	decreased cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20161201	MGI			PMID:22357600
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0014167	ectopic bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1323506	Rbfox2	RNA binding protein, fox-1 homolog (C. elegans) 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:31241461
1323509	Dok3	docking protein 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1323509	Dok3	docking protein 3	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1323509	Dok3	docking protein 3	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1323509	Dok3	docking protein 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1323509	Dok3	docking protein 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1323509	Dok3	docking protein 3	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1323509	Dok3	docking protein 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1323509	Dok3	docking protein 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20191128	MGI			PMID:17363732
1323509	Dok3	docking protein 3	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20191128	MGI			PMID:17363732
1323509	Dok3	docking protein 3	gene	MP:0004202	pulmonary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1323509	Dok3	docking protein 3	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20191128	MGI			PMID:17363732
1323509	Dok3	docking protein 3	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1323509	Dok3	docking protein 3	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1323509	Dok3	docking protein 3	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1323509	Dok3	docking protein 3	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20191128	MGI			PMID:17363732
1323509	Dok3	docking protein 3	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20548287
1323509	Dok3	docking protein 3	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1323509	Dok3	docking protein 3	gene	MP:0010829	increased bronchioalveolar stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139980
1323509	Dok3	docking protein 3	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:17363732
1323509	Dok3	docking protein 3	gene	MP:0020155	enhanced humoral immune response		IAGP		N	RGD:5509061	20191128	MGI			PMID:17363732
1323510	Akr1c21	aldo-keto reductase family 1, member C21	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20240530	MGI			PMID:34590152
1323510	Akr1c21	aldo-keto reductase family 1, member C21	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20240530	MGI			PMID:34590152
1323510	Akr1c21	aldo-keto reductase family 1, member C21	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20240530	MGI			PMID:34590152
1323510	Akr1c21	aldo-keto reductase family 1, member C21	gene	MP:0014437	increased interleukin level		IAGP		N	RGD:5509061	20240530	MGI			PMID:34590152
1323511	Slc25a45	solute carrier family 25, member 45	gene	MP:0003978	decreased circulating carnitine level		IAGP		N	RGD:5509061	20251204	MGI			PMID:41075780
1323511	Slc25a45	solute carrier family 25, member 45	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20251204	MGI			PMID:41075780
1323511	Slc25a45	solute carrier family 25, member 45	gene	MP:0021145	abnormal amino acid derivative level		IAGP		N	RGD:5509061	20251204	MGI			PMID:41075780
1323513	Hemk2	HemK methyltransferase 2, ETF1 glutamine and histone H4 lysine	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606008
1323513	Hemk2	HemK methyltransferase 2, ETF1 glutamine and histone H4 lysine	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606008
1323513	Hemk2	HemK methyltransferase 2, ETF1 glutamine and histone H4 lysine	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606008
1323513	Hemk2	HemK methyltransferase 2, ETF1 glutamine and histone H4 lysine	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606008
1323513	Hemk2	HemK methyltransferase 2, ETF1 glutamine and histone H4 lysine	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606008
1323513	Hemk2	HemK methyltransferase 2, ETF1 glutamine and histone H4 lysine	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20606008
1323515	Orc2	origin recognition complex, subunit 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1323515	Orc2	origin recognition complex, subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323515	Orc2	origin recognition complex, subunit 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1323517	Cdadc1	cytidine and dCMP deaminase domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20251127	MGI			PMID:40324085
1323517	Cdadc1	cytidine and dCMP deaminase domain containing 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20250911	MGI			PMID:40504152
1323517	Cdadc1	cytidine and dCMP deaminase domain containing 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20250911	MGI			PMID:40504152
1323519	1700030K09Rik	RIKEN cDNA 1700030K09 gene	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1323519	1700030K09Rik	RIKEN cDNA 1700030K09 gene	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1323520	P4htm	prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum)	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22955912
1323520	P4htm	prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum)	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:22955912
1323520	P4htm	prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum)	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22955912
1323520	P4htm	prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum)	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22955912
1323520	P4htm	prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum)	gene	MP:0011286	decreased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22955912
1323521	Focad	focadhesin	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210826	MGI			
1323521	Focad	focadhesin	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210826	MGI			
1323521	Focad	focadhesin	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210826	MGI			
1323521	Focad	focadhesin	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20210826	MGI			
1323521	Focad	focadhesin	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20210826	MGI			
1323521	Focad	focadhesin	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1323521	Focad	focadhesin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24667635
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11100122
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11100122
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11100122
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0001928	abnormal ovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11100122
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24667635
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11100122
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24667635
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:24667635
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20260507	MGI			PMID:40966276
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20260507	MGI			PMID:40966276
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20260507	MGI			PMID:40966276
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:11100122
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24667635
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24667635
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0009648	abnormal superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:11100122
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0014842	increased interferon-gamma level		IAGP		N	RGD:5509061	20260507	MGI			PMID:40966276
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:11100122
1323523	Nrip1	nuclear receptor interacting protein 1	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:11100122
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20181227	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20181227	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20181227	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170105	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20211125	MGI			PMID:32693673
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20170105	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20211125	MGI			PMID:32693673
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20170105	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201022	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1323528	Laptm4b	lysosomal-associated protein transmembrane 4B	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20211125	MGI			PMID:32693673
1323535	Abhd4	abhydrolase domain containing 4	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1323535	Abhd4	abhydrolase domain containing 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1323535	Abhd4	abhydrolase domain containing 4	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200416	MGI			PMID:25853435
1323535	Abhd4	abhydrolase domain containing 4	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200416	MGI			PMID:25853435
1323538	Scoc	short coiled-coil protein	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1323538	Scoc	short coiled-coil protein	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220519	MGI			
1323538	Scoc	short coiled-coil protein	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20231207	MGI			
1323538	Scoc	short coiled-coil protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1323540	Nudt16l1	nudix hydrolase 16 like 1	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1323540	Nudt16l1	nudix hydrolase 16 like 1	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1323540	Nudt16l1	nudix hydrolase 16 like 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1323542	Carnmt1	carnosine N-methyltransferase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1323542	Carnmt1	carnosine N-methyltransferase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20231102	MGI			PMID:37612136
1323542	Carnmt1	carnosine N-methyltransferase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260402	MGI			PMID:39201474
1323542	Carnmt1	carnosine N-methyltransferase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1323542	Carnmt1	carnosine N-methyltransferase 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20231102	MGI			PMID:37612136
1323542	Carnmt1	carnosine N-methyltransferase 1	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20231102	MGI			PMID:37612136
1323544	Slc22a12	solute carrier family 22 (organic anion/cation transporter), member 12	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18270321
1323544	Slc22a12	solute carrier family 22 (organic anion/cation transporter), member 12	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18270321
1323544	Slc22a12	solute carrier family 22 (organic anion/cation transporter), member 12	gene	MP:0009810	increased urine uric acid level		IAGP		N	RGD:5509061	20180517	MGI			PMID:20544513
1323544	Slc22a12	solute carrier family 22 (organic anion/cation transporter), member 12	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20180517	MGI			PMID:20544513
1323544	Slc22a12	solute carrier family 22 (organic anion/cation transporter), member 12	gene	MP:0011537	uraturia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18270321
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16249189
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855448
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20230119	MGI			
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16249189
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855448
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230119	MGI			
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0010540	long stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323546	Mtmr2	myotubularin related protein 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15557122
1323547	Cyp2r1	cytochrome P450, family 2, subfamily r, polypeptide 1	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20170223	MGI			PMID:24019477
1323547	Cyp2r1	cytochrome P450, family 2, subfamily r, polypeptide 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20170223	MGI			PMID:24019477
1323547	Cyp2r1	cytochrome P450, family 2, subfamily r, polypeptide 1	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20170223	MGI			PMID:24019477
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339376
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20220519	MGI			
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21478856
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339376
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339376
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20220519	MGI			
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339376
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0004930	small epididymis		IEA		N	RGD:5509061	20220519	MGI			
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339376
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339376
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17339376
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1323548	Syce2	synaptonemal complex central element protein 2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1323549	Cenpl	centromere protein L	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0000282	abnormal interatrial septum morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20240523	MGI			
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20240523	MGI			
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20191107	MGI			PMID:28475869
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0004094	abnormal M line morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20191107	MGI			PMID:28475869
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20191107	MGI			PMID:28475869
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20191107	MGI			PMID:28475869
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0010509	decreased P wave amplitude		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0010511	shortened PR interval		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0010634	increased QRS amplitude		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0014921	decreased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0030567	abnormal I band morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29183906
1323551	Smarcd3	SWI/SNF related BAF chromatin remodeling complex subunit D3	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:29183906
1323552	Tex46	testis expressed 46	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20241114	MGI			PMID:38516277
1323552	Tex46	testis expressed 46	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20241114	MGI			PMID:38516277
1323552	Tex46	testis expressed 46	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20241114	MGI			PMID:38516277
1323552	Tex46	testis expressed 46	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20241114	MGI			PMID:38516277
1323552	Tex46	testis expressed 46	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20241114	MGI			PMID:38516277
1323552	Tex46	testis expressed 46	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20241114	MGI			PMID:38516277
1323552	Tex46	testis expressed 46	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20241114	MGI			PMID:38516277
1323552	Tex46	testis expressed 46	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20241114	MGI			PMID:38516277
1323552	Tex46	testis expressed 46	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20241114	MGI			PMID:38516277
1323554	Pus1	pseudouridine synthase 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20260402	MGI			
1323554	Pus1	pseudouridine synthase 1	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1323554	Pus1	pseudouridine synthase 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1323554	Pus1	pseudouridine synthase 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1323554	Pus1	pseudouridine synthase 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1323554	Pus1	pseudouridine synthase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20260528	MGI			PMID:38450158
1323554	Pus1	pseudouridine synthase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1323554	Pus1	pseudouridine synthase 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20161222	MGI			PMID:27197761
1323554	Pus1	pseudouridine synthase 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20260528	MGI			PMID:38450158
1323554	Pus1	pseudouridine synthase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20260528	MGI			PMID:38450158
1323554	Pus1	pseudouridine synthase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20260528	MGI			PMID:38450158
1323554	Pus1	pseudouridine synthase 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20161222	MGI			PMID:27197761
1323554	Pus1	pseudouridine synthase 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20260528	MGI			PMID:38450158
1323554	Pus1	pseudouridine synthase 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1323554	Pus1	pseudouridine synthase 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20161222	MGI			PMID:27197761
1323554	Pus1	pseudouridine synthase 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20161222	MGI			PMID:27197761
1323554	Pus1	pseudouridine synthase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1323554	Pus1	pseudouridine synthase 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20260528	MGI			PMID:38450158
1323554	Pus1	pseudouridine synthase 1	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20260528	MGI			PMID:38450158
1323554	Pus1	pseudouridine synthase 1	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20161222	MGI			PMID:27197761
1323554	Pus1	pseudouridine synthase 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20161222	MGI			PMID:27197761
1323554	Pus1	pseudouridine synthase 1	gene	MP:0014955	increased mitochondria enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260528	MGI			PMID:38450158
1323554	Pus1	pseudouridine synthase 1	gene	MP:0014956	decreased mitochondria enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260528	MGI			PMID:38450158
1323554	Pus1	pseudouridine synthase 1	gene	MP:0031739	impaired translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:38450158
1323556	Twf1	twinfilin actin binding protein 1	gene	MP:0001191	abnormal skin condition		IEA		N	RGD:5509061	20141003	MGI			
1323556	Twf1	twinfilin actin binding protein 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1323556	Twf1	twinfilin actin binding protein 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20230420	MGI			PMID:31000436
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20190404	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:30569039
1323558	Rec114	REC114 meiotic recombination protein	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:30569039
1323560	Cdc25c	cell division cycle 25C	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21283624
1323560	Cdc25c	cell division cycle 25C	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21283624
1323560	Cdc25c	cell division cycle 25C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21283624
1323560	Cdc25c	cell division cycle 25C	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273838
1323560	Cdc25c	cell division cycle 25C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273838
1323560	Cdc25c	cell division cycle 25C	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11359894
1323560	Cdc25c	cell division cycle 25C	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273838
1323560	Cdc25c	cell division cycle 25C	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21283624
1323560	Cdc25c	cell division cycle 25C	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273838
1323560	Cdc25c	cell division cycle 25C	gene	MP:0008142	decreased small intestinal villus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21283624
1323560	Cdc25c	cell division cycle 25C	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21283624
1323560	Cdc25c	cell division cycle 25C	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21283624
1323560	Cdc25c	cell division cycle 25C	gene	MP:0010159	abnormal enterocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21283624
1323560	Cdc25c	cell division cycle 25C	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21283624
1323560	Cdc25c	cell division cycle 25C	gene	MP:0013958	decreased small intestine length		IAGP		N	RGD:5509061	20160310	MGI			PMID:19273838
1323560	Cdc25c	cell division cycle 25C	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20160310	MGI			PMID:19273838
1323561	Slc9b2	solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20231207	MGI			
1323561	Slc9b2	solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23720317
1323561	Slc9b2	solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23720317
1323561	Slc9b2	solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23720317
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191128	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191128	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191128	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20220519	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191128	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191128	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191128	MGI			
1323564	Actr8	ARP8 actin-related protein 8	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241128	MGI			
1323570	Epx	eosinophil peroxidase	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1323570	Epx	eosinophil peroxidase	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20181227	MGI			
1323570	Epx	eosinophil peroxidase	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630390
1323570	Epx	eosinophil peroxidase	gene	MP:0005061	abnormal eosinophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11466391
1323570	Epx	eosinophil peroxidase	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1323570	Epx	eosinophil peroxidase	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20150528	MGI			PMID:25514040
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820125
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:25514040
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20171026	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0003053	delayed tooth eruption		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20150528	MGI			PMID:25514040
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0003761	arched palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820125
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004553	absent tracheal cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004674	thin ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0009900	vomer bone hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0010981	abnormal branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820125
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820125
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446778
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997399
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820125
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0011425	abnormal kidney interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820125
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0030192	downturned snout		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0030259	mandibular condyloid process hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0030285	mandibular coronoid process hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0030377	zygomatic arch hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0030467	abnormal cranial cartilage development		IAGP		N	RGD:5509061	20221110	MGI			PMID:31130868
1323572	Trps1	transcriptional repressor GATA binding 1	gene	MP:0031459	maxillary zygomatic process hypoplasia		IAGP		N	RGD:5509061	20221201	MGI			PMID:31130868
1323574	Iqgap1	IQ motif containing GTPase activating protein 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1323574	Iqgap1	IQ motif containing GTPase activating protein 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1323574	Iqgap1	IQ motif containing GTPase activating protein 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1323574	Iqgap1	IQ motif containing GTPase activating protein 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
1323574	Iqgap1	IQ motif containing GTPase activating protein 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180285
1323574	Iqgap1	IQ motif containing GTPase activating protein 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180285
1323574	Iqgap1	IQ motif containing GTPase activating protein 1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1323574	Iqgap1	IQ motif containing GTPase activating protein 1	gene	MP:0005210	disorganized stomach mucosa		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611248
1323574	Iqgap1	IQ motif containing GTPase activating protein 1	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611248
1323578	Kif22	kinesin family member 22	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329364
1323578	Kif22	kinesin family member 22	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329364
1323578	Kif22	kinesin family member 22	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329364
1323578	Kif22	kinesin family member 22	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18329364
1323579	Ctif	CBP80/20-dependent translation initiation factor	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1323579	Ctif	CBP80/20-dependent translation initiation factor	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20240523	MGI			
1323579	Ctif	CBP80/20-dependent translation initiation factor	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20221027	MGI			
1323579	Ctif	CBP80/20-dependent translation initiation factor	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20240523	MGI			
1323581	Bivm	basic, immunoglobulin-like variable motif containing	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1323581	Bivm	basic, immunoglobulin-like variable motif containing	gene	MP:0013406	abnormal epidermal immune compartment		IEA		N	RGD:5509061	20201231	MGI			
1323584	Zfr	zinc finger RNA binding protein	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11283266
1323584	Zfr	zinc finger RNA binding protein	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11283266
1323584	Zfr	zinc finger RNA binding protein	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11283266
1323584	Zfr	zinc finger RNA binding protein	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11283266
1323584	Zfr	zinc finger RNA binding protein	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11283266
1323592	S100a11	S100 calcium binding protein A11	gene	MP:0002673	abnormal sperm number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14579419
1323601	Rhbdl3	rhomboid like 3	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20181227	MGI			
1323601	Rhbdl3	rhomboid like 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323603	Slirp	SRA stem-loop interacting RNA binding protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23976951
1323603	Slirp	SRA stem-loop interacting RNA binding protein	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23976951
1323603	Slirp	SRA stem-loop interacting RNA binding protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23976951
1323603	Slirp	SRA stem-loop interacting RNA binding protein	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:23976951
1323603	Slirp	SRA stem-loop interacting RNA binding protein	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:23976951
1323605	Vgll2	vestigial like family member 2	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20190912	MGI			PMID:28769032
1323605	Vgll2	vestigial like family member 2	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20190912	MGI			PMID:28769032
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000746	weakness		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001326	retina degeneration		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002772	brachypodia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0002993	autoimmune arthritis		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0004674	thin ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20231207	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0008974	proportional dwarf		IEA		N	RGD:5509061	20200430	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0009346	decreased trabecular bone thickness		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20230119	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0010869	decreased bone trabecula number		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0010879	decreased trabecular bone volume		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0010933	decreased trabecular bone connectivity density		IEA		N	RGD:5509061	20141003	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31754016
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0013616	decreased volumetric bone mineral density		IEA		N	RGD:5509061	20150319	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0014106	delayed chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0020010	decreased bone mineral density of femur		IEA		N	RGD:5509061	20220915	MGI			
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0020138	delayed bone mineralization		IAGP		N	RGD:5509061	20220915	MGI			PMID:22280990
1323607	Chsy1	chondroitin sulfate synthase 1	gene	MP:0021186	decreased bone mineral density of vertebrae		IEA		N	RGD:5509061	20220915	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0001694	absent egg cylinders		IEA		N	RGD:5509061	20191205	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191205	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0013241	embryo tissue necrosis		IEA		N	RGD:5509061	20191205	MGI			
1323618	Ccdc59	coiled-coil domain containing 59	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1323620	Slc25a38	solute carrier family 25, member 38	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1323622	Flnb	filamin, beta	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:24551245
1323622	Flnb	filamin, beta	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20181227	MGI			
1323622	Flnb	filamin, beta	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1323622	Flnb	filamin, beta	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:24551245
1323622	Flnb	filamin, beta	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20160310	MGI			PMID:24551245
1323622	Flnb	filamin, beta	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0003410	abnormal artery development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20160310	MGI			PMID:24551245
1323622	Flnb	filamin, beta	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1323622	Flnb	filamin, beta	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20160310	MGI			PMID:24551245
1323622	Flnb	filamin, beta	gene	MP:0004441	small occipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0004674	thin ribs		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0004683	absent intervertebral disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20160310	MGI			PMID:24551245
1323622	Flnb	filamin, beta	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20160310	MGI			PMID:24551245
1323622	Flnb	filamin, beta	gene	MP:0006429	abnormal hyaline cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0008155	decreased diameter of radius		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0008157	decreased diameter of ulna		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20160310	MGI			PMID:24551245
1323622	Flnb	filamin, beta	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1323622	Flnb	filamin, beta	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1323622	Flnb	filamin, beta	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
1323622	Flnb	filamin, beta	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17635842
1323622	Flnb	filamin, beta	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323622	Flnb	filamin, beta	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150917	MGI			PMID:23979929
1323622	Flnb	filamin, beta	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0014289	decreased distal limb length		IAGP		N	RGD:5509061	20230824	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0020487	abnormal middle cerebral artery morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:17360453
1323622	Flnb	filamin, beta	gene	MP:0021186	decreased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:17510210
1323622	Flnb	filamin, beta	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:17606870
1323622	Flnb	filamin, beta	gene	MP:0030797	joint laxity		IAGP		N	RGD:5509061	20181011	MGI			PMID:17510210
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0000371	diluted coat color		IEA		N	RGD:5509061	20111116	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12548288
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6776948
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0002412	increased susceptibility to bacterial infection		IEA		N	RGD:5509061	20111116	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2369371
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20240523	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0005100	abnormal choroid pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12548288
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0005102	abnormal iris pigmentation		IEA		N	RGD:5509061	20231207	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0005172	decreased eye pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:12548288
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2369371
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0005408	hypopigmentation		IEA		N	RGD:5509061	20180215	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0009379	abnormal foot pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0009557	decreased platelet ADP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6776948
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0011277	decreased tail pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0011279	decreased ear pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0011568	decreased foot pigmentation		IEA		N	RGD:5509061	20150108	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0012122	abnormal iris transillumination		IEA		N	RGD:5509061	20231207	MGI			
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:6696991
1323624	Hps5	HPS5, biogenesis of lysosomal organelles complex 2 subunit 2	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230119	MGI			
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0001574	abnormal oxygen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0004560	abnormal chorionic plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230119	MGI			
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1323628	Ss18	SS18, subunit of BAF chromatin remodeling complex	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1323632	Ttll6	tubulin tyrosine ligase-like family, member 6	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1323632	Ttll6	tubulin tyrosine ligase-like family, member 6	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1323633	Chd3	chromodomain helicase DNA binding protein 3	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1323633	Chd3	chromodomain helicase DNA binding protein 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1323633	Chd3	chromodomain helicase DNA binding protein 3	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:32658897
1323633	Chd3	chromodomain helicase DNA binding protein 3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:32658897
1323633	Chd3	chromodomain helicase DNA binding protein 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:32658897
1323633	Chd3	chromodomain helicase DNA binding protein 3	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:32658897
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0010889	small alveolar lamellar bodies		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323636	Mcrip1	MAPK regulated corepressor interacting protein 1	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20190912	MGI			PMID:31240265
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20220324	MGI			PMID:34942119
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20220324	MGI			PMID:34942119
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20220324	MGI			PMID:34942119
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220324	MGI			PMID:34942119
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1323638	Anapc7	anaphase promoting complex subunit 7	gene	MP:0020421	increased freezing behavior		IAGP		N	RGD:5509061	20220324	MGI			PMID:34942119
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296732
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296732
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296732
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296732
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0002634	abnormal sensorimotor gating		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0002895	abnormal otolithic membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296732
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420276
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296732
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296732
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296732
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
1323641	Cmah	cytidine monophospho-N-acetylneuraminic acid hydroxylase	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20668298
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20201022	MGI			
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20181227	MGI			
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160804	MGI			
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141030	MGI			PMID:24386439
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20221215	MGI			
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20170413	MGI			PMID:25220394
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0011240	abnormal fetal derived definitive erythrocyte morphology		IAGP		N	RGD:5509061	20170413	MGI			PMID:25220394
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0011243	decreased fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20170413	MGI			PMID:25220394
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm		IAGP		N	RGD:5509061	20170413	MGI			PMID:27381259
1323643	Cpeb4	cytoplasmic polyadenylation element binding protein 4	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260611	MGI			PMID:25220394
1323648	Chd1l	chromodomain helicase DNA binding protein 1-like	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210401	MGI			PMID:33333017
1323648	Chd1l	chromodomain helicase DNA binding protein 1-like	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210401	MGI			PMID:33333017
1323648	Chd1l	chromodomain helicase DNA binding protein 1-like	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20210401	MGI			PMID:33333017
1323648	Chd1l	chromodomain helicase DNA binding protein 1-like	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20210401	MGI			PMID:33333017
1323648	Chd1l	chromodomain helicase DNA binding protein 1-like	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210401	MGI			PMID:33333017
1323648	Chd1l	chromodomain helicase DNA binding protein 1-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210401	MGI			PMID:33333017
1323648	Chd1l	chromodomain helicase DNA binding protein 1-like	gene	MP:0011999	abnormal tail length		IEA		N	RGD:5509061	20210826	MGI			
1323650	Rnf20	ring finger protein 20	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1323650	Rnf20	ring finger protein 20	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1323650	Rnf20	ring finger protein 20	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0009310	increased large intestine adenocarcinoma incidence		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0009314	increased colon adenocarcinoma incidence		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1323650	Rnf20	ring finger protein 20	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323650	Rnf20	ring finger protein 20	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1323650	Rnf20	ring finger protein 20	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20210722	MGI			PMID:26854224
1323650	Rnf20	ring finger protein 20	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1323653	Bap1	Brca1 associated protein 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1323653	Bap1	Brca1 associated protein 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1323653	Bap1	Brca1 associated protein 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20201231	MGI			
1323653	Bap1	Brca1 associated protein 1	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1323653	Bap1	Brca1 associated protein 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20151022	MGI			PMID:24928783
1323653	Bap1	Brca1 associated protein 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20151022	MGI			PMID:24928783
1323653	Bap1	Brca1 associated protein 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1323653	Bap1	Brca1 associated protein 1	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20151022	MGI			PMID:24928783
1323653	Bap1	Brca1 associated protein 1	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0010309	increased mesothelioma incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0010348	increased pancreatic islet cell carcinoma incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20151022	MGI			PMID:24928783
1323653	Bap1	Brca1 associated protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1323653	Bap1	Brca1 associated protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323653	Bap1	Brca1 associated protein 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1323653	Bap1	Brca1 associated protein 1	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20151022	MGI			PMID:24928783
1323653	Bap1	Brca1 associated protein 1	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0012436	increased colon tumor incidence		IAGP		N	RGD:5509061	20170202	MGI			PMID:26896281
1323653	Bap1	Brca1 associated protein 1	gene	MP:0014713	abnormal erythrocyte basophilic stippling		IAGP		N	RGD:5509061	20250814	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:22878500
1323653	Bap1	Brca1 associated protein 1	gene	MP:0030025	giant platelets		IAGP		N	RGD:5509061	20170803	MGI			PMID:22878500
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20160811	MGI			
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20160811	MGI			
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20160811	MGI			
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21987787
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1323658	Asf1a	anti-silencing function 1A histone chaperone	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1323661	Nans	N-acetylneuraminic acid synthase (sialic acid synthase)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1323661	Nans	N-acetylneuraminic acid synthase (sialic acid synthase)	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1323661	Nans	N-acetylneuraminic acid synthase (sialic acid synthase)	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1323661	Nans	N-acetylneuraminic acid synthase (sialic acid synthase)	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1323661	Nans	N-acetylneuraminic acid synthase (sialic acid synthase)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201022	MGI			
1323661	Nans	N-acetylneuraminic acid synthase (sialic acid synthase)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1323661	Nans	N-acetylneuraminic acid synthase (sialic acid synthase)	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210128	MGI			
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20190502	MGI			
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0010187	decreased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1323662	Itfg2	integrin alpha FG-GAP repeat containing 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323666	1810055G02Rik	RIKEN cDNA 1810055G02 gene	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20240523	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0000297	abnormal atrioventricular cushion morphology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0004201	fetal growth retardation		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:9199343
1323668	Npat	nuclear protein in the AT region	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9199343
1323668	Npat	nuclear protein in the AT region	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0011493	double ureter		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0012111	failure of morula compaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:9199343
1323668	Npat	nuclear protein in the AT region	gene	MP:0013815	abnormal digastric muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0013943	abnormal ureter topology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0013966	abnormal infrahyoid muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0013977	symmetric azygos veins		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0013996	abnormal vertebral artery origin		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0014023	abnormal intestine placement		IEA		N	RGD:5509061	20170504	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0014087	retrolental blood		IEA		N	RGD:5509061	20180628	MGI			
1323668	Npat	nuclear protein in the AT region	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1323672	Sphkap	SPHK1 interactor, AKAP domain containing	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20201210	MGI			PMID:28396589
1323672	Sphkap	SPHK1 interactor, AKAP domain containing	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20201210	MGI			PMID:28396589
1323672	Sphkap	SPHK1 interactor, AKAP domain containing	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20201210	MGI			PMID:28396589
1323672	Sphkap	SPHK1 interactor, AKAP domain containing	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20201210	MGI			PMID:28396589
1323672	Sphkap	SPHK1 interactor, AKAP domain containing	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20201210	MGI			PMID:28396589
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17657313
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449664
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17657313
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17657313
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449664
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20211021	MGI			
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449664
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0005000	abnormal immune tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17657313
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0005630	increased lung weight		IEA		N	RGD:5509061	20211021	MGI			
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449664
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449664
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16449664
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008240	abnormal spleen marginal zone macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17657313
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17657313
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1323675	Siglec1	sialic acid binding Ig-like lectin 1, sialoadhesin	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107704
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15205536
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15205536
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15205536
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15205536
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0003395	abnormal subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0003819	increased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15205536
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0004044	aortic dissection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0006265	increased pulse pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0006278	aortic aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:24076219
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0008775	abnormal heart ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20170608	MGI			PMID:26980189
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24076219
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15205536
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107704
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0009871	abnormal aorta tunica adventitia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15205536
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0010468	abnormal thoracic aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0010470	dilated ascending aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0010661	ascending aorta aneurysm		IAGP		N	RGD:5509061	20150924	MGI			PMID:25255451
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293478
1323680	Mus81	MUS81 structure-specific endonuclease subunit	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15205536
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20241121	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20201022	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210826	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210826	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210520	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20201022	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20230601	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210520	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323688	Pole2	polymerase (DNA directed), epsilon 2 (p59 subunit)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1323691	Rbbp6	retinoblastoma binding protein 6, ubiquitin ligase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470788
1323691	Rbbp6	retinoblastoma binding protein 6, ubiquitin ligase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470788
1323691	Rbbp6	retinoblastoma binding protein 6, ubiquitin ligase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470788
1323691	Rbbp6	retinoblastoma binding protein 6, ubiquitin ligase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470788
1323691	Rbbp6	retinoblastoma binding protein 6, ubiquitin ligase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470788
1323693	Galnt12	polypeptide N-acetylgalactosaminyltransferase 12	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1323693	Galnt12	polypeptide N-acetylgalactosaminyltransferase 12	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1323693	Galnt12	polypeptide N-acetylgalactosaminyltransferase 12	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1323699	B3gat3	beta-1,3-glucuronyltransferase 3	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1323699	B3gat3	beta-1,3-glucuronyltransferase 3	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1323699	B3gat3	beta-1,3-glucuronyltransferase 3	gene	MP:0006204	embryonic lethality before implantation		IAGP		N	RGD:5509061	20151217	MGI			PMID:20164174
1323699	B3gat3	beta-1,3-glucuronyltransferase 3	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20151217	MGI			PMID:20164174
1323699	B3gat3	beta-1,3-glucuronyltransferase 3	gene	MP:0013289	abnormal mitotic cytokinesis		IAGP		N	RGD:5509061	20151217	MGI			PMID:20164174
1323701	Ca6	carbonic anhydrase 6	gene	MP:0002389	abnormal Peyer's patch follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20835760
1323702	Zc2hc1a	zinc finger, C2HC-type containing 1A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1323702	Zc2hc1a	zinc finger, C2HC-type containing 1A	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1323702	Zc2hc1a	zinc finger, C2HC-type containing 1A	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1323702	Zc2hc1a	zinc finger, C2HC-type containing 1A	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1323704	Uqcrb	ubiquinol-cytochrome c reductase binding protein	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1323704	Uqcrb	ubiquinol-cytochrome c reductase binding protein	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1323704	Uqcrb	ubiquinol-cytochrome c reductase binding protein	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1323704	Uqcrb	ubiquinol-cytochrome c reductase binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15738389
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9087432
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9087432
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968018
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15738389
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9087432
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15738389
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18826952
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20161103	MGI			PMID:25041126
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15738389
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18826952
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15738389
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15738389
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15738389
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968018
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968018
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18826952
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20161103	MGI			PMID:25041126
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968018
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968018
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12968018
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20161103	MGI			PMID:18826952
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9087432
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9501099
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:12968018
1323706	Nfe2l1	nuclear factor, erythroid derived 2,-like 1	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:9501099
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20181227	MGI			
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20220407	MGI			PMID:35238669
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20160421	MGI			
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201231	MGI			
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20220407	MGI			PMID:35238669
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20220407	MGI			PMID:35238669
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20220407	MGI			PMID:35238669
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1323710	Usp38	ubiquitin specific peptidase 38	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
1323717	Nbea	neurobeachin	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1323717	Nbea	neurobeachin	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20230601	MGI			
1323717	Nbea	neurobeachin	gene	MP:0000738	impaired muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071111
1323717	Nbea	neurobeachin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153818
1323717	Nbea	neurobeachin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071111
1323717	Nbea	neurobeachin	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153818
1323717	Nbea	neurobeachin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153818
1323717	Nbea	neurobeachin	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071111
1323717	Nbea	neurobeachin	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153818
1323717	Nbea	neurobeachin	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153818
1323717	Nbea	neurobeachin	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071111
1323717	Nbea	neurobeachin	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071111
1323717	Nbea	neurobeachin	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1323717	Nbea	neurobeachin	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153818
1323717	Nbea	neurobeachin	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153818
1323717	Nbea	neurobeachin	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153818
1323717	Nbea	neurobeachin	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20230601	MGI			
1323717	Nbea	neurobeachin	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071111
1323717	Nbea	neurobeachin	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1323717	Nbea	neurobeachin	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071111
1323717	Nbea	neurobeachin	gene	MP:0006320	abnormal interscapular fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071111
1323717	Nbea	neurobeachin	gene	MP:0006320	abnormal interscapular fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153818
1323717	Nbea	neurobeachin	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1323717	Nbea	neurobeachin	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1323717	Nbea	neurobeachin	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071111
1323717	Nbea	neurobeachin	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20221215	MGI			
1323717	Nbea	neurobeachin	gene	MP:0014379	decreased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:19723784
1323717	Nbea	neurobeachin	gene	MP:0015055	decreased synapse density		IAGP		N	RGD:5509061	20260813	MGI			PMID:19723784
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160414	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20160414	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20160414	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001348	abnormal lacrimal gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0002819	abnormal dental pulp cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003930	abnormal tooth hard tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0003933	abnormal cementum morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0010870	absent bone trabeculae		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20160414	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0011498	abnormal glomerular capsule parietal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0011504	abnormal limb long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0012175	flat face		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0013251	dental pulp necrosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0014104	decreased chondrocyte apoptosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160616	MGI			PMID:22615579
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20160414	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030132	periodontium inflammation		IAGP		N	RGD:5509061	20171005	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030153	dental pulp inflammation		IAGP		N	RGD:5509061	20171005	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030223	mandibular hyperostosis		IAGP		N	RGD:5509061	20171019	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030462	tooth abscess		IAGP		N	RGD:5509061	20171221	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030463	apical tooth abscess		IAGP		N	RGD:5509061	20171221	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030466	alveolar process atrophy		IAGP		N	RGD:5509061	20171221	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030484	abnormal osteocyte lacuna morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030485	abnormal osteocyte lacunocanalicular system morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030486	abnormal osteocyte canaliculus morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030487	abnormal osteocyte dendritic process morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030490	periodontal pocket		IAGP		N	RGD:5509061	20171228	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030493	abnormal tooth root morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030500	conical molar		IAGP		N	RGD:5509061	20180125	MGI			PMID:22732358
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030515	periodontal ligament necrosis		IAGP		N	RGD:5509061	20180111	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030517	detached junctional epithelium		IAGP		N	RGD:5509061	20180111	MGI			PMID:25479552
1323720	Fam20c	FAM20C, golgi associated secretory pathway kinase	gene	MP:0030542	abnormal dentin development		IAGP		N	RGD:5509061	20180215	MGI			PMID:22732358
1323723	Slc25a24	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20211118	MGI			PMID:25599384
1323723	Slc25a24	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
1323723	Slc25a24	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20211118	MGI			PMID:25599384
1323723	Slc25a24	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20211118	MGI			PMID:25599384
1323723	Slc25a24	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20211118	MGI			PMID:25599384
1323723	Slc25a24	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1323723	Slc25a24	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1323725	Rgma	repulsive guidance molecule family member A	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749425
1323725	Rgma	repulsive guidance molecule family member A	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749425
1323725	Rgma	repulsive guidance molecule family member A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749425
1323725	Rgma	repulsive guidance molecule family member A	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749425
1323725	Rgma	repulsive guidance molecule family member A	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749425
1323725	Rgma	repulsive guidance molecule family member A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749425
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880528
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645530
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22492726
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880528
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880528
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880528
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22492726
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0011707	impaired fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22492726
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0014365	impaired short-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:23554489
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20170223	MGI			PMID:22492726
1323729	Arpc3	actin related protein 2/3 complex, subunit 3	gene	MP:0020415	abnormal fibroblast chemotaxis		IAGP		N	RGD:5509061	20170223	MGI			PMID:22492726
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16888024
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16888024
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16888024
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081770
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081770
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16888024
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16888024
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18097056
1323731	Ptgdr2	prostaglandin D2 receptor 2	gene	MP:0009815	decreased prostaglandin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16888024
1323732	Pld6	phospholipase D family member 6	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397847
1323732	Pld6	phospholipase D family member 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397847
1323732	Pld6	phospholipase D family member 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397848
1323732	Pld6	phospholipase D family member 6	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397848
1323732	Pld6	phospholipase D family member 6	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397848
1323732	Pld6	phospholipase D family member 6	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397847
1323732	Pld6	phospholipase D family member 6	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397847
1323732	Pld6	phospholipase D family member 6	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397848
1323732	Pld6	phospholipase D family member 6	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397847
1323732	Pld6	phospholipase D family member 6	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397847
1323732	Pld6	phospholipase D family member 6	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397848
1323732	Pld6	phospholipase D family member 6	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397847
1323732	Pld6	phospholipase D family member 6	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397848
1323732	Pld6	phospholipase D family member 6	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397847
1323732	Pld6	phospholipase D family member 6	gene	MP:0008878	abnormal DNA methylation during gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21397847
1323732	Pld6	phospholipase D family member 6	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:21397847
1323736	Ckap4	cytoskeleton-associated protein 4	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20250508	MGI			
1323736	Ckap4	cytoskeleton-associated protein 4	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20250508	MGI			
1323736	Ckap4	cytoskeleton-associated protein 4	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1323736	Ckap4	cytoskeleton-associated protein 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323739	Erf	Ets2 repressor factor	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:23354439
1323739	Erf	Ets2 repressor factor	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23354439
1323739	Erf	Ets2 repressor factor	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23354439
1323739	Erf	Ets2 repressor factor	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20181227	MGI			
1323739	Erf	Ets2 repressor factor	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190808	MGI			
1323739	Erf	Ets2 repressor factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20220811	MGI			
1323739	Erf	Ets2 repressor factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23354439
1323739	Erf	Ets2 repressor factor	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1323739	Erf	Ets2 repressor factor	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20181227	MGI			
1323739	Erf	Ets2 repressor factor	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323739	Erf	Ets2 repressor factor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0012090	midbrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0012099	decreased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0012134	absent umbilical cord		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0012264	hindbrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17502352
1323739	Erf	Ets2 repressor factor	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1323741	Mroh4	maestro heat-like repeat family member 4	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201022	MGI			
1323742	Sowahb	sosondowah ankyrin repeat domain family member B	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1323742	Sowahb	sosondowah ankyrin repeat domain family member B	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1323742	Sowahb	sosondowah ankyrin repeat domain family member B	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1323744	Zscan2	zinc finger and SCAN domain containing 2	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20201231	MGI			
1323746	Ccl21a	C-C motif chemokine ligand 21 (serine)	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180426	MGI			PMID:28611158
1323746	Ccl21a	C-C motif chemokine ligand 21 (serine)	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20180426	MGI			PMID:28611158
1323746	Ccl21a	C-C motif chemokine ligand 21 (serine)	gene	MP:0004918	abnormal negative T cell selection		IAGP		N	RGD:5509061	20180426	MGI			PMID:28611158
1323746	Ccl21a	C-C motif chemokine ligand 21 (serine)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180426	MGI			PMID:28611158
1323746	Ccl21a	C-C motif chemokine ligand 21 (serine)	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20180426	MGI			PMID:28611158
1323746	Ccl21a	C-C motif chemokine ligand 21 (serine)	gene	MP:0012765	decreased alpha-beta T cell number		IAGP		N	RGD:5509061	20180426	MGI			PMID:28611158
1323746	Ccl21a	C-C motif chemokine ligand 21 (serine)	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20180426	MGI			PMID:28611158
1323746	Ccl21a	C-C motif chemokine ligand 21 (serine)	gene	MP:0020220	decreased tear production		IAGP		N	RGD:5509061	20180426	MGI			PMID:28611158
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773073
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773073
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773073
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20260514	MGI			PMID:17224479
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773073
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773073
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773073
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17224479
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17224479
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17224479
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17224479
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0006142	abnormal sinoatrial node conduction		IAGP		N	RGD:5509061	20260514	MGI			PMID:17224479
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17224479
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20260514	MGI			PMID:17224479
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11773073
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20260514	MGI			PMID:17224479
1323752	Asph	aspartate-beta-hydroxylase	gene	MP:0031734	doublet premature ventricular contraction		IAGP		N	RGD:5509061	20260716	MGI			PMID:17224479
1323754	Rdh11	retinol dehydrogenase 11	gene	MP:0003011	delayed dark adaptation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634683
1323754	Rdh11	retinol dehydrogenase 11	gene	MP:0003011	delayed dark adaptation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790565
1323754	Rdh11	retinol dehydrogenase 11	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634683
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20240523	MGI			
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20240523	MGI			
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20240523	MGI			
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14512015
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20221020	MGI			PMID:30157434
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586755
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:30157434
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20221020	MGI			PMID:30157434
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20221020	MGI			PMID:30157434
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20221020	MGI			PMID:30157434
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0011062	abnormal outer hair cell kinocilium morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:30157434
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20221020	MGI			PMID:30157434
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20240523	MGI			
1323756	Cobl	cordon-bleu WH2 repeat	gene	MP:0030944	abnormal pericentriolar material morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:30157434
1323757	Alg14	asparagine-linked glycosylation 14	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191205	MGI			
1323757	Alg14	asparagine-linked glycosylation 14	gene	MP:0008527	embryonic lethality at implantation		IEA		N	RGD:5509061	20241017	MGI			
1323757	Alg14	asparagine-linked glycosylation 14	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323757	Alg14	asparagine-linked glycosylation 14	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20240523	MGI			
1323757	Alg14	asparagine-linked glycosylation 14	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20181227	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20181227	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210128	MGI			PMID:32954300
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20210128	MGI			PMID:32954300
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20210128	MGI			PMID:32954300
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20210128	MGI			PMID:32954300
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20210128	MGI			PMID:32954300
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20210128	MGI			PMID:32954300
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20181227	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20210128	MGI			PMID:32954300
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20181227	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20210128	MGI			PMID:32954300
1323760	Minar2	membrane integral NOTCH2 associated receptor 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1323763	Etv1	ets variant 1	gene	MP:0000959	abnormal somatic sensory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493690
1323763	Etv1	ets variant 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493690
1323763	Etv1	ets variant 1	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
1323763	Etv1	ets variant 1	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10850491
1323763	Etv1	ets variant 1	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15836427
1323763	Etv1	ets variant 1	gene	MP:0000988	abnormal pacinian corpuscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493690
1323763	Etv1	ets variant 1	gene	MP:0000999	abnormal golgi tendon organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0001000	absent golgi tendon organ		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10850491
1323763	Etv1	ets variant 1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10850491
1323763	Etv1	ets variant 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10850491
1323763	Etv1	ets variant 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1323763	Etv1	ets variant 1	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20141003	MGI			PMID:10850491
1323763	Etv1	ets variant 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
1323763	Etv1	ets variant 1	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10850491
1323763	Etv1	ets variant 1	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12741988
1323763	Etv1	ets variant 1	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
1323763	Etv1	ets variant 1	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10850491
1323763	Etv1	ets variant 1	gene	MP:0006006	increased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
1323763	Etv1	ets variant 1	gene	MP:0008468	absent muscle spindles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0008485	increased muscle spindle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891988
1323763	Etv1	ets variant 1	gene	MP:0008486	decreased muscle spindle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522042
1323763	Etv1	ets variant 1	gene	MP:0030996	decreased pacinian corpuscle number		IAGP		N	RGD:5509061	20200130	MGI			PMID:16493690
1323763	Etv1	ets variant 1	gene	MP:0030998	small pacinian corpuscles		IAGP		N	RGD:5509061	20200130	MGI			PMID:16493690
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:18393392
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20170209	MGI			PMID:18393392
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20170209	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170209	MGI			
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0002425	abnormal susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20170209	MGI			PMID:19729839
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20170209	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20170209	MGI			PMID:18393392
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20201119	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20170209	MGI			PMID:11452127
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20170209	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0009008	delayed estrous cycle		IAGP		N	RGD:5509061	20170209	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0009012	short diestrus		IAGP		N	RGD:5509061	20170209	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0009014	prolonged proestrus		IAGP		N	RGD:5509061	20170209	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0009322	increased splenocyte apoptosis		IAGP		N	RGD:5509061	20201119	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0009396	small endometrial glands		IAGP		N	RGD:5509061	20170209	MGI			PMID:18393392
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0009853	decreased Sertoli cell phagocytosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:18159085
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20170209	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20201119	MGI			PMID:10227296
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0014551	impaired neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:18787040
1323765	Axl	AXL receptor tyrosine kinase	gene	MP:0031168	abnormal brain thrombosis		IAGP		N	RGD:5509061	20201119	MGI			PMID:11452127
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210128	MGI			
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0002798	abnormal active avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0003862	decreased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1323767	Pak5	p21 (RAC1) activated kinase 5	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18675265
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200109	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20200109	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200109	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20200109	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20200109	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20200109	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0013667	increased immature NK cell number		IAGP		N	RGD:5509061	20200109	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0013672	decreased mature NK cell number		IAGP		N	RGD:5509061	20200109	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0013699	abnormal immature NK cell morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0020950	decreased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:31024568
1323769	Kctd9	potassium channel tetramerisation domain containing 9	gene	MP:0031047	decreased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:31024568
1323771	Shmt1	serine hydroxymethyltransferase 1 (soluble)	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18644786
1323771	Shmt1	serine hydroxymethyltransferase 1 (soluble)	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1323771	Shmt1	serine hydroxymethyltransferase 1 (soluble)	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22438825
1323771	Shmt1	serine hydroxymethyltransferase 1 (soluble)	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1323771	Shmt1	serine hydroxymethyltransferase 1 (soluble)	gene	MP:0030625	increased circulating cysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:18644786
1323771	Shmt1	serine hydroxymethyltransferase 1 (soluble)	gene	MP:0030688	decreased circulating cystathionine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:18644786
1323773	Sprr1b	small proline-rich protein 1B	gene	MP:0011471	decreased urine creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1323775	Nt5c3	5'-nucleotidase, cytosolic III	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20230119	MGI			
1323775	Nt5c3	5'-nucleotidase, cytosolic III	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1323775	Nt5c3	5'-nucleotidase, cytosolic III	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20231207	MGI			
1323775	Nt5c3	5'-nucleotidase, cytosolic III	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1323775	Nt5c3	5'-nucleotidase, cytosolic III	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1323775	Nt5c3	5'-nucleotidase, cytosolic III	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1323775	Nt5c3	5'-nucleotidase, cytosolic III	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1323775	Nt5c3	5'-nucleotidase, cytosolic III	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1323778	Xpo4	exportin 4	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230119	MGI			
1323778	Xpo4	exportin 4	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1323778	Xpo4	exportin 4	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230119	MGI			
1323778	Xpo4	exportin 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20240314	MGI			
1323778	Xpo4	exportin 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1323778	Xpo4	exportin 4	gene	MP:0012006	abnormal hippocampus physiology		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323778	Xpo4	exportin 4	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1323778	Xpo4	exportin 4	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20221103	MGI			PMID:36182935
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323781	Lynx1	Ly6/neurotoxin 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950157
1323783	Zfp503	zinc finger protein 503	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20210520	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200402	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20240314	MGI			PMID:32170006
1323783	Zfp503	zinc finger protein 503	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20240314	MGI			PMID:32170006
1323783	Zfp503	zinc finger protein 503	gene	MP:0004103	abnormal ventral striatum morphology		IAGP		N	RGD:5509061	20240314	MGI			PMID:32170006
1323783	Zfp503	zinc finger protein 503	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20231207	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20240314	MGI			PMID:32170006
1323783	Zfp503	zinc finger protein 503	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20231207	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0009208	abnormal female genitalia morphology		IEA		N	RGD:5509061	20260402	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0009953	abnormal olfactory tubercle morphology		IAGP		N	RGD:5509061	20240314	MGI			PMID:32170006
1323783	Zfp503	zinc finger protein 503	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240314	MGI			PMID:32170006
1323783	Zfp503	zinc finger protein 503	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323783	Zfp503	zinc finger protein 503	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20241121	MGI			
1323789	Sox15	SRY (sex determining region Y)-box 15	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367664
1323789	Sox15	SRY (sex determining region Y)-box 15	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863505
1323789	Sox15	SRY (sex determining region Y)-box 15	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20211125	MGI			PMID:15367664
1323789	Sox15	SRY (sex determining region Y)-box 15	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:15367664
1323790	Uba2	ubiquitin-like modifier activating enzyme 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20191017	MGI			PMID:29872538
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20230601	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230601	MGI			
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20191017	MGI			PMID:29872538
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:29872538
1323794	Peak1	pseudopodium-enriched atypical kinase 1	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20191017	MGI			PMID:29872538
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0008932	abnormal embryonic tissue physiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0010039	abnormal trophoblast giant cell proliferation		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20181220	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:29447390
1323796	Pold3	polymerase (DNA-directed), delta 3, accessory subunit	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:29447390
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220519	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20170105	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20170105	MGI			
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0008656	abnormal interleukin-1 beta secretion		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20170525	MGI			PMID:26582950
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:25222142
1323797	Pgam5	phosphoglycerate mutase family member 5	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20170105	MGI			
1323799	Plekhf2	pleckstrin homology and FYVE domain containing 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1323799	Plekhf2	pleckstrin homology and FYVE domain containing 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1323799	Plekhf2	pleckstrin homology and FYVE domain containing 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20241121	MGI			
1323799	Plekhf2	pleckstrin homology and FYVE domain containing 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1323799	Plekhf2	pleckstrin homology and FYVE domain containing 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230601	MGI			
1323799	Plekhf2	pleckstrin homology and FYVE domain containing 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230601	MGI			
1323799	Plekhf2	pleckstrin homology and FYVE domain containing 2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1323799	Plekhf2	pleckstrin homology and FYVE domain containing 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1323799	Plekhf2	pleckstrin homology and FYVE domain containing 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20241121	MGI			
1323801	Cnih1	cornichon family AMPA receptor auxiliary protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1323801	Cnih1	cornichon family AMPA receptor auxiliary protein 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1323801	Cnih1	cornichon family AMPA receptor auxiliary protein 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620511
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001800	abnormal humoral immune response		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20190411	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620511
1323809	Stk4	serine/threonine kinase 4	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620511
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620511
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620511
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002491	decreased IgD level		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002494	increased IgM level		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002497	increased IgE level		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20170223	MGI			PMID:26131558
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0004978	decreased B-1 B cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005141	liver hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005425	increased macrophage cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008048	abnormal memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IEA		N	RGD:5509061	20190411	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19692642
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008122	decreased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008126	increased dendritic cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008180	abnormal marginal zone B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19073936
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008891	decreased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080689
1323809	Stk4	serine/threonine kinase 4	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0009658	increased placenta apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620511
1323809	Stk4	serine/threonine kinase 4	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0011018	pulmonary hyaline membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620511
1323809	Stk4	serine/threonine kinase 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19878874
1323809	Stk4	serine/threonine kinase 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0011139	increased lung endothelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620511
1323809	Stk4	serine/threonine kinase 4	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:20080598
1323809	Stk4	serine/threonine kinase 4	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:19786569
1323809	Stk4	serine/threonine kinase 4	gene	MP:0013649	decreased CD11b-high dendritic cell number		IEA		N	RGD:5509061	20190411	MGI			
1323809	Stk4	serine/threonine kinase 4	gene	MP:0014348	decreased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:19339990
1323809	Stk4	serine/threonine kinase 4	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20190411	MGI			
1323813	Agmo	alkylglycerol monooxygenase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20220407	MGI			PMID:33726865
1323813	Agmo	alkylglycerol monooxygenase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20220407	MGI			PMID:33726865
1323813	Agmo	alkylglycerol monooxygenase	gene	MP:0012220	abnormal ether lipid level		IAGP		N	RGD:5509061	20240808	MGI			PMID:36690320
1323816	Senp3	SUMO/sentrin specific peptidase 3	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20160804	MGI			
1323816	Senp3	SUMO/sentrin specific peptidase 3	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978061
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2338491
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230119	MGI			
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:2338491
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978061
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978061
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2338491
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230119	MGI			
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978061
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:2338491
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978061
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2338491
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2338491
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978061
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2338491
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978061
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:2338491
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8978061
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:8835524
1323820	Lnpk	lunapark, ER junction formation factor	gene	MP:0030886	decreased radius size		IAGP		N	RGD:5509061	20181101	MGI			PMID:2338491
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723506
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723506
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20160218	MGI			
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0006038	increased mitochondrial fission		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723506
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0008725	increased heart atrium size		IEA		N	RGD:5509061	20170105	MGI			
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723506
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723506
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723506
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723506
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723506
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21723506
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1323822	Cox15	cytochrome c oxidase assembly protein 15	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:21723506
1323825	Tex10	testis expressed gene 10	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160526	MGI			PMID:25936917
1323825	Tex10	testis expressed gene 10	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20160526	MGI			PMID:25936917
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713933
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0001188	hyperpigmentation		IEA		N	RGD:5509061	20111116	MGI			
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0001224	abnormal keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141218	MGI			PMID:18821597
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0001968	abnormal touch/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:15994880
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:15277941
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:15994880
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653560
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653560
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0002671	belted		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713933
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713933
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:10374067
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653560
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652101
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:5713933
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:767180
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141218	MGI			PMID:18821597
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20171228	MGI			PMID:18715234
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20190110	MGI			PMID:27134165
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0004270	analgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15994880
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0004382	abnormal hair follicle melanogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1098946
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0005077	abnormal melanogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988713
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0005409	darkened coat color		IEA		N	RGD:5509061	20111116	MGI			
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0006370	abnormal hair follicle pheomelanosome pheomelanin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652101
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0009388	abnormal epidermal melanocyte morphology		IAGP		N	RGD:5509061	20190110	MGI			PMID:27134165
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0009928	abnormal pinna hair pigmentation		IEA		N	RGD:5509061	20141003	MGI			
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0009933	abnormal tail hair pigmentation		IEA		N	RGD:5509061	20160428	MGI			
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0011277	decreased tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653560
1323827	Mc1r	melanocortin 1 receptor	gene	MP:0011279	decreased ear pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653560
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000576	clubfoot		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18031680
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18031680
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098484
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18031680
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18031680
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18031680
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20180208	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18031680
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098484
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0004082	abnormal habenula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0004103	abnormal ventral striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0004165	abnormal lateral geniculate nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0008129	absent brain internal capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0008129	absent brain internal capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23968836
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098484
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19391113
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1323831	Mycbp2	MYC binding protein 2, E3 ubiquitin protein ligase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1323833	Akt1s1	AKT1 substrate 1	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20160526	MGI			PMID:24583056
1323833	Akt1s1	AKT1 substrate 1	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24583056
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0003675	kidney cyst		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0004017	duplex kidney		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21725307
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0006123	tricuspid valve atresia		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0006130	pulmonary valve atresia		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0010202	focal dorsal hair loss		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0010406	common atrium		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0010413	complete atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0010865	prenatal growth retardation		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0011053	decreased respiratory motile cilia number		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0011060	abnormal kinocilium morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0011254	superior-inferior ventricles		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0011510	biventricular, discordant atrioventricular connection		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0013197	decreased embryonic cilium number		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0013205	abnormal nonmotile primary cilium morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331854	Cc2d2a	coiled-coil and C2 domain containing 2A	gene	MP:0013214	decreased embryonic neuroepithelium primary cilium number		IAGP		N	RGD:5509061	20160623	MGI			PMID:24947469
1331856	Pdilt	protein disulfide isomerase-like, testis expressed	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357757
1331856	Pdilt	protein disulfide isomerase-like, testis expressed	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357757
1331856	Pdilt	protein disulfide isomerase-like, testis expressed	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220303	MGI			PMID:22357757
1331857	Rmp64	ribonuclease MRP subunit p64	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:26178919
1331857	Rmp64	ribonuclease MRP subunit p64	gene	MP:0008830	abnormal nucleolus morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:26178919
1331857	Rmp64	ribonuclease MRP subunit p64	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:26178919
1331857	Rmp64	ribonuclease MRP subunit p64	gene	MP:0012129	failure of blastocyst formation		IAGP		N	RGD:5509061	20150910	MGI			PMID:26178919
1331858	Gphn	gephyrin	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15689563
1331858	Gphn	gephyrin	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9812897
1331858	Gphn	gephyrin	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15689563
1331858	Gphn	gephyrin	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15689563
1331858	Gphn	gephyrin	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15689563
1331858	Gphn	gephyrin	gene	MP:0001400	hyperresponsive		IAGP		N	RGD:5509061	20141003	MGI			PMID:9812897
1331858	Gphn	gephyrin	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9812897
1331858	Gphn	gephyrin	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9812897
1331858	Gphn	gephyrin	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9812897
1331858	Gphn	gephyrin	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:9812897
1331858	Gphn	gephyrin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209184
1331858	Gphn	gephyrin	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15689563
1331858	Gphn	gephyrin	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15689563
1331858	Gphn	gephyrin	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11056469
1331858	Gphn	gephyrin	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15689563
1331858	Gphn	gephyrin	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9812897
1331860	Tmem127	transmembrane protein 127	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20160804	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334765
1331860	Tmem127	transmembrane protein 127	gene	MP:0000579	abnormal nail morphology		IEA		N	RGD:5509061	20200402	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20200402	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24334765
1331860	Tmem127	transmembrane protein 127	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20141030	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20210128	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181227	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20141030	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20210128	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20141030	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0012767	increased KLRG1-positive NK cell number		IEA		N	RGD:5509061	20201022	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0012768	decreased KLRG1-positive NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0013023	decreased Ly6C high monocyte number		IEA		N	RGD:5509061	20160804	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0013025	increased Ly6C low monocyte number		IEA		N	RGD:5509061	20160804	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0013426	decreased memory-marker NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0013427	increased memory-marker NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1331860	Tmem127	transmembrane protein 127	gene	MP:0013774	decreased KLRG1-positive T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1331863	Astn1	astrotactin 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331863	Astn1	astrotactin 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331863	Astn1	astrotactin 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331863	Astn1	astrotactin 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331863	Astn1	astrotactin 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331863	Astn1	astrotactin 1	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331863	Astn1	astrotactin 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331863	Astn1	astrotactin 1	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331863	Astn1	astrotactin 1	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331863	Astn1	astrotactin 1	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861479
1331865	Cd200r1	CD200 receptor 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424714
1331865	Cd200r1	CD200 receptor 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20220922	MGI			PMID:34921782
1331865	Cd200r1	CD200 receptor 1	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17667818
1331865	Cd200r1	CD200 receptor 1	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20220922	MGI			PMID:34921782
1331865	Cd200r1	CD200 receptor 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20200310	MGI			PMID:17667818
1331865	Cd200r1	CD200 receptor 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:17667818
1331865	Cd200r1	CD200 receptor 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082204
1331865	Cd200r1	CD200 receptor 1	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082204
1331865	Cd200r1	CD200 receptor 1	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:17667818
1331865	Cd200r1	CD200 receptor 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082204
1331865	Cd200r1	CD200 receptor 1	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23082204
1331865	Cd200r1	CD200 receptor 1	gene	MP:0020954	decreased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20220922	MGI			PMID:34921782
1331865	Cd200r1	CD200 receptor 1	gene	MP:0031025	decreased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:23082204
1331866	Syne4	spectrin repeat containing, nuclear envelope family member 4	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23348741
1331866	Syne4	spectrin repeat containing, nuclear envelope family member 4	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23348741
1331866	Syne4	spectrin repeat containing, nuclear envelope family member 4	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23348741
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0000416	sparse hair		IEA		N	RGD:5509061	20141003	MGI			
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0001923	reduced female fertility		IEA		N	RGD:5509061	20141003	MGI			
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0003849	greasy coat		IEA		N	RGD:5509061	20141003	MGI			
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0005251	blepharitis		IEA		N	RGD:5509061	20141003	MGI			
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0009608	abnormal epidermal lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0009794	sebaceous gland hyperplasia		IEA		N	RGD:5509061	20141003	MGI			
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331867	Scd2	stearoyl-Coenzyme A desaturase 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118274
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20943660
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0010754	abnormal heart left ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331868	Mylk3	myosin light chain kinase 3	gene	MP:0012735	abnormal response to exercise		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095280
1331869	Rhebl1	Ras homolog enriched in brain like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21238928
1331869	Rhebl1	Ras homolog enriched in brain like 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21238928
1331871	Klhdc7a	kelch domain containing 7A	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210422	MGI			
1331873	Spon1	spondin 1, (f-spondin) extracellular matrix protein	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:24875054
1331873	Spon1	spondin 1, (f-spondin) extracellular matrix protein	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20150903	MGI			PMID:24875054
1331873	Spon1	spondin 1, (f-spondin) extracellular matrix protein	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20150903	MGI			PMID:24875054
1331873	Spon1	spondin 1, (f-spondin) extracellular matrix protein	gene	MP:0008838	decreased transforming growth factor beta level		IAGP		N	RGD:5509061	20150903	MGI			PMID:24875054
1331873	Spon1	spondin 1, (f-spondin) extracellular matrix protein	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20150903	MGI			PMID:24875054
1331873	Spon1	spondin 1, (f-spondin) extracellular matrix protein	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20150903	MGI			PMID:24875054
1331873	Spon1	spondin 1, (f-spondin) extracellular matrix protein	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20150903	MGI			PMID:24875054
1331873	Spon1	spondin 1, (f-spondin) extracellular matrix protein	gene	MP:0013623	increased femur compact bone thickness		IAGP		N	RGD:5509061	20150903	MGI			PMID:24875054
1331873	Spon1	spondin 1, (f-spondin) extracellular matrix protein	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20150903	MGI			PMID:24875054
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0008010	increased gastric adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0011273	prolonged excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20160218	MGI			PMID:26490870
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17349584
1331874	Lzts1	leucine zipper, putative tumor suppressor 1	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20230608	MGI			PMID:17349584
1331876	Ccdc47	coiled-coil domain containing 47	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17204322
1331876	Ccdc47	coiled-coil domain containing 47	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17204322
1331876	Ccdc47	coiled-coil domain containing 47	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17204322
1331876	Ccdc47	coiled-coil domain containing 47	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17204322
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331877	Crebrf	CREB3 regulatory factor	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20160811	MGI			PMID:23071095
1331878	Shkbp1	Sh3kbp1 binding protein 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20241121	MGI			
1331878	Shkbp1	Sh3kbp1 binding protein 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1331881	Iws1	IWS1, SUPT6 interacting protein	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20240627	MGI			
1331881	Iws1	IWS1, SUPT6 interacting protein	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1331881	Iws1	IWS1, SUPT6 interacting protein	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20181025	MGI			PMID:30208029
1331881	Iws1	IWS1, SUPT6 interacting protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1331881	Iws1	IWS1, SUPT6 interacting protein	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1331883	Nup210	nucleoporin 210	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20211223	MGI			PMID:29736031
1331883	Nup210	nucleoporin 210	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1331883	Nup210	nucleoporin 210	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1331883	Nup210	nucleoporin 210	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1331883	Nup210	nucleoporin 210	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20211223	MGI			PMID:29736031
1331883	Nup210	nucleoporin 210	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20211223	MGI			PMID:29736031
1331883	Nup210	nucleoporin 210	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1331883	Nup210	nucleoporin 210	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30323813
1331883	Nup210	nucleoporin 210	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20211223	MGI			PMID:29736031
1331883	Nup210	nucleoporin 210	gene	MP:0008073	abnormal CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20211223	MGI			PMID:29736031
1331883	Nup210	nucleoporin 210	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30323813
1331883	Nup210	nucleoporin 210	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20211223	MGI			PMID:29736031
1331883	Nup210	nucleoporin 210	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30323813
1331883	Nup210	nucleoporin 210	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30323813
1331883	Nup210	nucleoporin 210	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30323813
1331883	Nup210	nucleoporin 210	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30323813
1331883	Nup210	nucleoporin 210	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30323813
1331883	Nup210	nucleoporin 210	gene	MP:0012762	abnormal alpha-beta T cell morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:30323813
1331883	Nup210	nucleoporin 210	gene	MP:0012765	decreased alpha-beta T cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30323813
1331883	Nup210	nucleoporin 210	gene	MP:0013772	increased effector memory T-helper cell number		IAGP		N	RGD:5509061	20211223	MGI			PMID:29736031
1331884	Dlgap3	DLG associated protein 3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713528
1331884	Dlgap3	DLG associated protein 3	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713528
1331884	Dlgap3	DLG associated protein 3	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713528
1331884	Dlgap3	DLG associated protein 3	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713528
1331884	Dlgap3	DLG associated protein 3	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713528
1331884	Dlgap3	DLG associated protein 3	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713528
1331884	Dlgap3	DLG associated protein 3	gene	MP:0003234	enhanced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713528
1331884	Dlgap3	DLG associated protein 3	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713528
1331884	Dlgap3	DLG associated protein 3	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713528
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1331887	Sdhaf2	succinate dehydrogenase complex assembly factor 2	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0009443	parthenogenesis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0011130	absent tertiary ovarian follicles		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0013507	increased ovary apoptosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331889	Tent5b	terminal nucleotidyltransferase 5B	gene	MP:0031474	increased female germ cell apoptosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1331890	Telo2	telomere maintenance 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160036
1331890	Telo2	telomere maintenance 2	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160036
1331890	Telo2	telomere maintenance 2	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160036
1331890	Telo2	telomere maintenance 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1331890	Telo2	telomere maintenance 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160036
1331890	Telo2	telomere maintenance 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331890	Telo2	telomere maintenance 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1331894	Nln	neurolysin (metallopeptidase M3 family)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24719317
1331894	Nln	neurolysin (metallopeptidase M3 family)	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141106	MGI			PMID:24719317
1331894	Nln	neurolysin (metallopeptidase M3 family)	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141106	MGI			PMID:24719317
1331894	Nln	neurolysin (metallopeptidase M3 family)	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141106	MGI			PMID:24719317
1331894	Nln	neurolysin (metallopeptidase M3 family)	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141106	MGI			PMID:24719317
1331894	Nln	neurolysin (metallopeptidase M3 family)	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141106	MGI			PMID:24719317
1331895	Sh3d19	SH3 domain protein D19	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20240523	MGI			
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20230622	MGI			PMID:25671302
1331899	Puf60	poly-U binding splicing factor 60	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1331901	Bud13	BUD13 homolog	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20241121	MGI			
1331901	Bud13	BUD13 homolog	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1331901	Bud13	BUD13 homolog	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20260402	MGI			
1331901	Bud13	BUD13 homolog	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
1331901	Bud13	BUD13 homolog	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1331901	Bud13	BUD13 homolog	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20260402	MGI			
1331901	Bud13	BUD13 homolog	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20260402	MGI			
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160211	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331903	Tysnd1	trypsin domain containing 1	gene	MP:0012216	decreased plasmalogen level		IAGP		N	RGD:5509061	20151126	MGI			PMID:23459139
1331904	Zbtb14	zinc finger and BTB domain containing 14	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1331904	Zbtb14	zinc finger and BTB domain containing 14	gene	MP:0000285	abnormal heart valve morphology		IEA		N	RGD:5509061	20141003	MGI			
1331904	Zbtb14	zinc finger and BTB domain containing 14	gene	MP:0000519	hydronephrosis		IEA		N	RGD:5509061	20141003	MGI			
1331904	Zbtb14	zinc finger and BTB domain containing 14	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20141003	MGI			
1331904	Zbtb14	zinc finger and BTB domain containing 14	gene	MP:0003675	kidney cyst		IEA		N	RGD:5509061	20141003	MGI			
1331904	Zbtb14	zinc finger and BTB domain containing 14	gene	MP:0004017	duplex kidney		IEA		N	RGD:5509061	20141003	MGI			
1331904	Zbtb14	zinc finger and BTB domain containing 14	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1331904	Zbtb14	zinc finger and BTB domain containing 14	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20201022	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20201022	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20201022	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003707	increased cell nucleus count		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20201022	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003902	abnormal cell mass		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0006204	embryonic lethality before implantation		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0009567	mitotic nondisjunction		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0010291	increased cardiovascular system tumor incidence		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20170824	MGI			PMID:26443207
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1331905	Nsmce2	NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:26443207
1331906	Rpain	RPA interacting protein	gene	MP:0005028	abnormal trophectoderm morphology		IEA		N	RGD:5509061	20240801	MGI			
1331906	Rpain	RPA interacting protein	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1331906	Rpain	RPA interacting protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331906	Rpain	RPA interacting protein	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1331906	Rpain	RPA interacting protein	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240801	MGI			
1331908	Arsg	arylsulfatase G	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20191219	MGI			PMID:26975023
1331908	Arsg	arylsulfatase G	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0004967	abnormal kidney epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0008242	abnormal perivascular macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20191219	MGI			PMID:26975023
1331908	Arsg	arylsulfatase G	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20191219	MGI			PMID:26975023
1331908	Arsg	arylsulfatase G	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20191219	MGI			PMID:26975023
1331908	Arsg	arylsulfatase G	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20191219	MGI			PMID:26975023
1331908	Arsg	arylsulfatase G	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0010369	abnormal thalamus neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689975
1331908	Arsg	arylsulfatase G	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20191219	MGI			PMID:26975023
1331908	Arsg	arylsulfatase G	gene	MP:0031148	abnormal liver sinusoidal endothelial cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:22689975
1331911	Clip3	CAP-GLY domain containing linker protein 3	gene	MP:0000738	impaired muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23482493
1331911	Clip3	CAP-GLY domain containing linker protein 3	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23482493
1331911	Clip3	CAP-GLY domain containing linker protein 3	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23482493
1331911	Clip3	CAP-GLY domain containing linker protein 3	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23482493
1331911	Clip3	CAP-GLY domain containing linker protein 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23482493
1331911	Clip3	CAP-GLY domain containing linker protein 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23482493
1331911	Clip3	CAP-GLY domain containing linker protein 3	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23482493
1331911	Clip3	CAP-GLY domain containing linker protein 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23482493
1331911	Clip3	CAP-GLY domain containing linker protein 3	gene	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:23482493
1331913	Trak2	trafficking protein, kinesin binding 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1331913	Trak2	trafficking protein, kinesin binding 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1331913	Trak2	trafficking protein, kinesin binding 2	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1331913	Trak2	trafficking protein, kinesin binding 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1331913	Trak2	trafficking protein, kinesin binding 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1331913	Trak2	trafficking protein, kinesin binding 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1331913	Trak2	trafficking protein, kinesin binding 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1331913	Trak2	trafficking protein, kinesin binding 2	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1331914	Dab2ip	disabled 2 interacting protein	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23326475
1331914	Dab2ip	disabled 2 interacting protein	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281285
1331914	Dab2ip	disabled 2 interacting protein	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281285
1331916	Mustn1	musculoskeletal, embryonic nuclear protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240404	MGI			PMID:38458566
1331916	Mustn1	musculoskeletal, embryonic nuclear protein 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20240404	MGI			PMID:38458566
1331916	Mustn1	musculoskeletal, embryonic nuclear protein 1	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:38458566
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160421	MGI			
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20160421	MGI			
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20160421	MGI			
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331917	Mfsd8	major facilitator superfamily domain containing 8	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141127	MGI			PMID:24423645
1331918	Ptpru	protein tyrosine phosphatase receptor type U	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220519	MGI			
1331918	Ptpru	protein tyrosine phosphatase receptor type U	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1331918	Ptpru	protein tyrosine phosphatase receptor type U	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1331918	Ptpru	protein tyrosine phosphatase receptor type U	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20170105	MGI			
1331920	Tomm40	translocase of outer mitochondrial membrane 40	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1331920	Tomm40	translocase of outer mitochondrial membrane 40	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1331920	Tomm40	translocase of outer mitochondrial membrane 40	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1331920	Tomm40	translocase of outer mitochondrial membrane 40	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1331920	Tomm40	translocase of outer mitochondrial membrane 40	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1331920	Tomm40	translocase of outer mitochondrial membrane 40	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1331920	Tomm40	translocase of outer mitochondrial membrane 40	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331920	Tomm40	translocase of outer mitochondrial membrane 40	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1331921	Large2	LARGE xylosyl- and glucuronyltransferase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160929	MGI			PMID:25138275
1331921	Large2	LARGE xylosyl- and glucuronyltransferase 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
1331921	Large2	LARGE xylosyl- and glucuronyltransferase 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20211021	MGI			
1331922	Nexn	nexilin	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20160804	MGI			PMID:26659360
1331922	Nexn	nexilin	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:32814711
1331922	Nexn	nexilin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20160804	MGI			PMID:26659360
1331922	Nexn	nexilin	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20160804	MGI			PMID:26659360
1331922	Nexn	nexilin	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20210401	MGI			PMID:32814711
1331922	Nexn	nexilin	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20160804	MGI			PMID:26659360
1331922	Nexn	nexilin	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20160804	MGI			PMID:26659360
1331922	Nexn	nexilin	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20160804	MGI			PMID:26659360
1331922	Nexn	nexilin	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20210401	MGI			PMID:32814711
1331922	Nexn	nexilin	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20160804	MGI			PMID:26659360
1331922	Nexn	nexilin	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20210401	MGI			PMID:32814711
1331922	Nexn	nexilin	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160804	MGI			PMID:26659360
1331922	Nexn	nexilin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210401	MGI			PMID:32814711
1331922	Nexn	nexilin	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20210401	MGI			PMID:32814711
1331922	Nexn	nexilin	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331922	Nexn	nexilin	gene	MP:0031147	abnormal ventricular thrombosis		IAGP		N	RGD:5509061	20210415	MGI			PMID:30982350
1331923	Rnase6	ribonuclease, RNase A family, 6	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210128	MGI			
1331923	Rnase6	ribonuclease, RNase A family, 6	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1331923	Rnase6	ribonuclease, RNase A family, 6	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20210128	MGI			
1331923	Rnase6	ribonuclease, RNase A family, 6	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210128	MGI			
1331924	Ints3	integrator complex subunit 3	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20201022	MGI			
1331924	Ints3	integrator complex subunit 3	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1331924	Ints3	integrator complex subunit 3	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1331924	Ints3	integrator complex subunit 3	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1331924	Ints3	integrator complex subunit 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1331924	Ints3	integrator complex subunit 3	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20201022	MGI			
1331924	Ints3	integrator complex subunit 3	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1331924	Ints3	integrator complex subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331924	Ints3	integrator complex subunit 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1331925	Cenpt	centromere protein T	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1331925	Cenpt	centromere protein T	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1331925	Cenpt	centromere protein T	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331925	Cenpt	centromere protein T	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20241121	MGI			
1331925	Cenpt	centromere protein T	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1331926	Mvb12a	multivesicular body subunit 12A	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20260402	MGI			
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210422	MGI			
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20210422	MGI			
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0010207	abnormal telomere morphology		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210422	MGI			
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160602	MGI			PMID:23459151
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20150312	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0014281	hindlimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:22940690
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0014281	hindlimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:23408915
1331927	Nabp2	nucleic acid binding protein 2	gene	MP:0014473	increased pulmonary alveolus wall thickness		IAGP		N	RGD:5509061	20240704	MGI			PMID:23408915
1331928	Adgrl2	adhesion G protein-coupled receptor L2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20210128	MGI			PMID:31206334
1331928	Adgrl2	adhesion G protein-coupled receptor L2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20141003	MGI			
1331928	Adgrl2	adhesion G protein-coupled receptor L2	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:31206334
1331928	Adgrl2	adhesion G protein-coupled receptor L2	gene	MP:0003922	abnormal heart right atrium morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:31206334
1331928	Adgrl2	adhesion G protein-coupled receptor L2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20210128	MGI			PMID:31206334
1331928	Adgrl2	adhesion G protein-coupled receptor L2	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20210128	MGI			PMID:31206334
1331928	Adgrl2	adhesion G protein-coupled receptor L2	gene	MP:0010580	decreased heart left ventricle size		IAGP		N	RGD:5509061	20210128	MGI			PMID:31206334
1331928	Adgrl2	adhesion G protein-coupled receptor L2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:31206334
1331928	Adgrl2	adhesion G protein-coupled receptor L2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1331929	Slc16a10	solute carrier family 16 (monocarboxylic acid transporters), member 10	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20160211	MGI			PMID:26438296
1331929	Slc16a10	solute carrier family 16 (monocarboxylic acid transporters), member 10	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:23045339
1331929	Slc16a10	solute carrier family 16 (monocarboxylic acid transporters), member 10	gene	MP:0003311	aminoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:23045339
1331929	Slc16a10	solute carrier family 16 (monocarboxylic acid transporters), member 10	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23045339
1331929	Slc16a10	solute carrier family 16 (monocarboxylic acid transporters), member 10	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23045339
1331929	Slc16a10	solute carrier family 16 (monocarboxylic acid transporters), member 10	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:23045339
1331929	Slc16a10	solute carrier family 16 (monocarboxylic acid transporters), member 10	gene	MP:0011468	abnormal urine amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23045339
1331929	Slc16a10	solute carrier family 16 (monocarboxylic acid transporters), member 10	gene	MP:0011470	increased urine creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23045339
1331929	Slc16a10	solute carrier family 16 (monocarboxylic acid transporters), member 10	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23045339
1331933	Gk5	glycerol kinase 5	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0008860	abnormal hair cycle telogen phase		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0009004	progressive hair loss		IEA		N	RGD:5509061	20181004	MGI			
1331933	Gk5	glycerol kinase 5	gene	MP:0009131	decreased white fat cell number		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20181011	MGI			
1331933	Gk5	glycerol kinase 5	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1331933	Gk5	glycerol kinase 5	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20180208	MGI			PMID:28607088
1331933	Gk5	glycerol kinase 5	gene	MP:0012764	increased alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1331934	Prom1	prominin 1	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718438
1331934	Prom1	prominin 1	gene	MP:0001324	abnormal eye pigmentation		IEA		N	RGD:5509061	20141218	MGI			
1331934	Prom1	prominin 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0001326	retina degeneration		IEA		N	RGD:5509061	20141218	MGI			
1331934	Prom1	prominin 1	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718438
1331934	Prom1	prominin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092805
1331934	Prom1	prominin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092805
1331934	Prom1	prominin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718438
1331934	Prom1	prominin 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19092805
1331934	Prom1	prominin 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331934	Prom1	prominin 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20141218	MGI			
1331934	Prom1	prominin 1	gene	MP:0012029	abnormal electroretinogram waveform feature		IEA		N	RGD:5509061	20141218	MGI			
1331934	Prom1	prominin 1	gene	MP:0012143	decreased a-wave amplitude		IEA		N	RGD:5509061	20141218	MGI			
1331934	Prom1	prominin 1	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:19718438
1331934	Prom1	prominin 1	gene	MP:0014333	short retina cone cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:19228982
1331934	Prom1	prominin 1	gene	MP:0014658	absent a-wave		IEA		N	RGD:5509061	20250410	MGI			
1331934	Prom1	prominin 1	gene	MP:0020439	absent b-wave		IEA		N	RGD:5509061	20250410	MGI			
1331934	Prom1	prominin 1	gene	MP:0020816	decreased photoreceptor outer segment number		IAGP		N	RGD:5509061	20200123	MGI			PMID:25414197
1331935	Poc5	POC5 centriolar protein	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20181227	MGI			
1331935	Poc5	POC5 centriolar protein	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20181227	MGI			
1331935	Poc5	POC5 centriolar protein	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1331935	Poc5	POC5 centriolar protein	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20260402	MGI			
1331935	Poc5	POC5 centriolar protein	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1331935	Poc5	POC5 centriolar protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0002244	abnormal turbinate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0003311	aminoaciduria		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0011229	abnormal vitamin C level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0011229	abnormal vitamin C level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22820017
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22820017
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0014975	decreased kidney enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22820017
1331936	Akr1a1	aldo-keto reductase family 1, member A1	gene	MP:0030884	rachitic rosary		IAGP		N	RGD:5509061	20200310	MGI			PMID:20410296
1331938	Trmt1	tRNA methyltransferase 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20181227	MGI			
1331938	Trmt1	tRNA methyltransferase 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1331938	Trmt1	tRNA methyltransferase 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1331938	Trmt1	tRNA methyltransferase 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20210128	MGI			
1331938	Trmt1	tRNA methyltransferase 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1331938	Trmt1	tRNA methyltransferase 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20210128	MGI			
1331938	Trmt1	tRNA methyltransferase 1	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1331938	Trmt1	tRNA methyltransferase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331939	Mettl18	methyltransferase like 18	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20240523	MGI			
1331939	Mettl18	methyltransferase like 18	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1331939	Mettl18	methyltransferase like 18	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220519	MGI			
1331939	Mettl18	methyltransferase like 18	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1331939	Mettl18	methyltransferase like 18	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1331940	Dlgap4	DLG associated protein 4	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1331940	Dlgap4	DLG associated protein 4	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1331940	Dlgap4	DLG associated protein 4	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1331940	Dlgap4	DLG associated protein 4	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1331940	Dlgap4	DLG associated protein 4	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1331940	Dlgap4	DLG associated protein 4	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20200402	MGI			
1331940	Dlgap4	DLG associated protein 4	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0020513	abnormal dendritic stubby spine morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:30664629
1331940	Dlgap4	DLG associated protein 4	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:30664629
1331941	Kcnk12	potassium channel, subfamily K, member 12	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1331943	Pou2f3	POU domain, class 2, transcription factor 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1331943	Pou2f3	POU domain, class 2, transcription factor 3	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:21572433
1331943	Pou2f3	POU domain, class 2, transcription factor 3	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242494
1331943	Pou2f3	POU domain, class 2, transcription factor 3	gene	MP:0004209	abnormal sweet taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21572433
1331943	Pou2f3	POU domain, class 2, transcription factor 3	gene	MP:0004210	abnormal bitter taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21572433
1331943	Pou2f3	POU domain, class 2, transcription factor 3	gene	MP:0004213	abnormal umami taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21572433
1331943	Pou2f3	POU domain, class 2, transcription factor 3	gene	MP:0006260	abnormal gustatory papilla taste bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21572433
1331943	Pou2f3	POU domain, class 2, transcription factor 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9242494
1331944	Fbln7	fibulin 7	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:29730503
1331944	Fbln7	fibulin 7	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:29730503
1331944	Fbln7	fibulin 7	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20191003	MGI			PMID:29730503
1331944	Fbln7	fibulin 7	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20191003	MGI			PMID:29730503
1331944	Fbln7	fibulin 7	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20191003	MGI			PMID:29730503
1331946	Arhgdig	Rho GDP dissociation inhibitor gamma	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054116
1331947	Nabp1	nucleic acid binding protein 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20180719	MGI			PMID:25917330
1331947	Nabp1	nucleic acid binding protein 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:25917330
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723493
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20170105	MGI			
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20170105	MGI			
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0002830	gallstones		IAGP		N	RGD:5509061	20141003	MGI			PMID:16724960
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16724960
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16724960
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0005084	abnormal gallbladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16724960
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065403
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16724960
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723493
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065403
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065403
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17065403
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19723493
1331948	Gpbar1	G protein-coupled bile acid receptor 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20220721	MGI			PMID:34329568
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0003925	abnormal cellular glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331949	Top1mt	DNA topoisomerase 1, mitochondrial	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22911747
1331953	Prelid1	PRELI domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22666421
1331954	Frmd4b	FERM domain containing 4B	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1331954	Frmd4b	FERM domain containing 4B	gene	MP:0005102	abnormal iris pigmentation		IEA		N	RGD:5509061	20241121	MGI			
1331954	Frmd4b	FERM domain containing 4B	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20200310	MGI			
1331954	Frmd4b	FERM domain containing 4B	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20241121	MGI			
1331955	Ubash3b	ubiquitin associated and SH3 domain containing, B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170323	MGI			PMID:12370296
1331955	Ubash3b	ubiquitin associated and SH3 domain containing, B	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20170323	MGI			PMID:14738763
1331955	Ubash3b	ubiquitin associated and SH3 domain containing, B	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20170323	MGI			PMID:14738763
1331955	Ubash3b	ubiquitin associated and SH3 domain containing, B	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20170323	MGI			PMID:14738763
1331955	Ubash3b	ubiquitin associated and SH3 domain containing, B	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20170323	MGI			PMID:14738763
1331955	Ubash3b	ubiquitin associated and SH3 domain containing, B	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20170323	MGI			PMID:14738763
1331956	Crip2	cysteine rich protein 2	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20151217	MGI			PMID:18256252
1331956	Crip2	cysteine rich protein 2	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20151217	MGI			PMID:18256252
1331958	Prkci	protein kinase C, iota	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322187
1331958	Prkci	protein kinase C, iota	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267237
1331958	Prkci	protein kinase C, iota	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267237
1331958	Prkci	protein kinase C, iota	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19835853
1331958	Prkci	protein kinase C, iota	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19835853
1331958	Prkci	protein kinase C, iota	gene	MP:0001318	pupil opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19835853
1331958	Prkci	protein kinase C, iota	gene	MP:0001320	small pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:19835853
1331958	Prkci	protein kinase C, iota	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19835853
1331958	Prkci	protein kinase C, iota	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267237
1331958	Prkci	protein kinase C, iota	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0001705	abnormal proximal-distal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267237
1331958	Prkci	protein kinase C, iota	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0002579	disorganized secondary lens fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:19835853
1331958	Prkci	protein kinase C, iota	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630453
1331958	Prkci	protein kinase C, iota	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19835853
1331958	Prkci	protein kinase C, iota	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0004559	small allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19835853
1331958	Prkci	protein kinase C, iota	gene	MP:0005199	abnormal iris pigment epithelium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19835853
1331958	Prkci	protein kinase C, iota	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630453
1331958	Prkci	protein kinase C, iota	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15630453
1331958	Prkci	protein kinase C, iota	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0008062	abnormal podocyte slit junction morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0008062	abnormal podocyte slit junction morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0008583	absent photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267237
1331958	Prkci	protein kinase C, iota	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267237
1331958	Prkci	protein kinase C, iota	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322187
1331958	Prkci	protein kinase C, iota	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0011190	thick embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279126
1331958	Prkci	protein kinase C, iota	gene	MP:0011483	renal glomerular synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0011869	detached podocyte		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0011870	abnormal podocyte polarity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19142224
1331958	Prkci	protein kinase C, iota	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0012081	absent heart tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0012104	small amniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23690951
1331958	Prkci	protein kinase C, iota	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0030020	decreased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0030022	decreased muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:17641777
1331958	Prkci	protein kinase C, iota	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:17641777
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0000324	increased mast cell number		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0002464	abnormal basophil physiology		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0002606	increased basophil cell number		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331960	Enpp3	ectonucleotide pyrophosphatase/phosphodiesterase 3	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160421	MGI			PMID:25692702
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461904
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461904
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22210510
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461904
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22210510
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461904
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461904
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22210510
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22210510
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461904
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22210510
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461904
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22210510
1331961	Arl6ip5	ADP-ribosylation factor-like 6 interacting protein 5	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250925	MGI			PMID:22461904
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20160915	MGI			PMID:24813896
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160915	MGI			PMID:24813896
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21926268
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20160915	MGI			PMID:24813896
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20160915	MGI			PMID:24813896
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20665729
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21926268
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040596
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0011016	increased core body temperature		IAGP		N	RGD:5509061	20160915	MGI			PMID:24813896
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20160915	MGI			PMID:24813896
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040596
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20160915	MGI			PMID:24813896
1331963	Appl1	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1	gene	MP:0020101	abnormal hepatic glucose production		IAGP		N	RGD:5509061	20160915	MGI			PMID:24813896
1331964	Prr13	proline rich 13	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20260402	MGI			
1331964	Prr13	proline rich 13	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18209067
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210128	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:10407043
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001380	decreased male mating frequency		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:18209067
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10407043
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:18209067
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18209067
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:10407043
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20210128	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10407043
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20260402	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210128	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18209067
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11376114
1331966	Npepps	aminopeptidase puromycin sensitive	gene	MP:0030610	absent teeth		IEA		N	RGD:5509061	20210520	MGI			
1331969	Oser1	oxidative stress responsive serine rich 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1331969	Oser1	oxidative stress responsive serine rich 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210520	MGI			
1331969	Oser1	oxidative stress responsive serine rich 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331971	Ptpn23	protein tyrosine phosphatase, non-receptor type 23	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1331971	Ptpn23	protein tyrosine phosphatase, non-receptor type 23	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1331971	Ptpn23	protein tyrosine phosphatase, non-receptor type 23	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1331971	Ptpn23	protein tyrosine phosphatase, non-receptor type 23	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1331971	Ptpn23	protein tyrosine phosphatase, non-receptor type 23	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378249
1331971	Ptpn23	protein tyrosine phosphatase, non-receptor type 23	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1331971	Ptpn23	protein tyrosine phosphatase, non-receptor type 23	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19378249
1331971	Ptpn23	protein tyrosine phosphatase, non-receptor type 23	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0012552	lactic acidosis		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331972	Acad9	acyl-Coenzyme A dehydrogenase family, member 9	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20221117	MGI			PMID:34556413
1331973	Scgb3a1	secretoglobin, family 3A, member 1	gene	MP:0011053	decreased respiratory motile cilia number		IAGP		N	RGD:5509061	20210204	MGI			PMID:30768367
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207730
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207730
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207730
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207730
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517118
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517118
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000568	ectopic digits		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000580	deformed nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517118
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22794264
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22794264
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986861
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001054	failure of neuromuscular synapse presynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001054	failure of neuromuscular synapse presynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986861
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001055	failure of neuromuscular synapse postsynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001055	failure of neuromuscular synapse postsynaptic differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986861
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517118
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517118
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517118
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517118
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22794264
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001678	thick apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207730
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207730
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001921	reduced fertility		IEA		N	RGD:5509061	20151015	MGI			
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986861
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20151015	MGI			
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207730
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20111116	MGI			
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517118
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20018657
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002772	brachypodia		IAGP		N	RGD:5509061	20230824	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22794264
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517118
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20151015	MGI			
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0004639	fused metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22794264
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207730
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20018657
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0006369	supernumerary incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20018657
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0008730	fused phalanges		IEA		N	RGD:5509061	20151015	MGI			
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986861
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0010932	increased trabecular bone connectivity density		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22794264
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986861
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22794264
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986861
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207730
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986861
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011298	ureter hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0011387	absent metanephric mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:20454682
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0013623	increased femur compact bone thickness		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0013785	abnormal mammary gland bud morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:17119023
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0030278	thick neurocranium		IAGP		N	RGD:5509061	20200430	MGI			PMID:28477420
1331974	Lrp4	low density lipoprotein receptor-related protein 4	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:20018657
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20180719	MGI			PMID:15070780
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20190328	MGI			PMID:29226825
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:12834911
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:16887279
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:8633004
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20190328	MGI			PMID:29226825
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20180719	MGI			PMID:15070780
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20180719	MGI			PMID:12834911
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001425	abnormal alcohol consumption		IAGP		N	RGD:5509061	20180719	MGI			PMID:9726280
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20180719	MGI			PMID:15070780
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20190328	MGI			PMID:29226825
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12834911
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0001968	abnormal touch/nociception		IAGP		N	RGD:5509061	20180719	MGI			PMID:8633004
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002629	hyperactivity elicited by ethanol administration		IAGP		N	RGD:5509061	20180719	MGI			PMID:9726280
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12458044
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12458044
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20180719	MGI			PMID:15070780
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002768	small adrenal glands		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20180719	MGI			PMID:9726280
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20180719	MGI			PMID:17652101
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20180719	MGI			PMID:9726280
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:16887279
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20180719	MGI			PMID:17467916
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005128	decreased adrenocorticotropin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20180719	MGI			PMID:15070780
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20190328	MGI			PMID:29226825
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005313	absent adrenal gland		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20180719	MGI			PMID:15070780
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20180719	MGI			PMID:15070780
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005661	decreased circulating adrenaline level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20180719	MGI			PMID:16887279
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0006370	abnormal hair follicle pheomelanosome pheomelanin content		IAGP		N	RGD:5509061	20180719	MGI			PMID:17652101
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:12458044
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:12458044
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:12458044
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:12458044
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20180719	MGI			PMID:17467916
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20180719	MGI			PMID:8633004
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20180719	MGI			PMID:12697680
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20180719	MGI			PMID:10470087
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20190328	MGI			PMID:29226825
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0014285	disorganized adrenal gland zona fasciculata		IAGP		N	RGD:5509061	20230907	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0014286	increased adrenal gland zona fasciculata size		IAGP		N	RGD:5509061	20230907	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0014287	decreased adrenal gland zona fasciculata size		IAGP		N	RGD:5509061	20230907	MGI			PMID:17095588
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0014441	decreased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:15070780
1331975	Pomc	pro-opiomelanocortin-alpha	gene	MP:0030770	increased urine adrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:16887279
1331976	Chct1	CHD1 helical C-terminal domain containing 1	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20230720	MGI			
1331976	Chct1	CHD1 helical C-terminal domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20141003	MGI			
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0000644	dextrocardia		IEA		N	RGD:5509061	20141003	MGI			
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0000694	spleen hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0001893	non-obstructive hydrocephaly		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210520	MGI			
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210520	MGI			
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0010152	abnormal brain ependyma morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0011055	abnormal respiratory motile cilium physiology		IEA		N	RGD:5509061	20141003	MGI			
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0011253	situs inversus with levocardia		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0011649	immotile respiratory cilia		IEA		N	RGD:5509061	20141003	MGI			
1331977	Odad3	outer dynein arm docking complex subunit 3	gene	MP:0012139	increased forebrain size		IAGP		N	RGD:5509061	20191003	MGI			PMID:31383820
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20151203	MGI			PMID:24049736
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360356
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360356
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360356
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360356
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360356
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200917	MGI			PMID:17360356
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0003916	decreased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519122
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141629
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141629
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141629
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20151203	MGI			PMID:24049736
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20519122
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:24049736
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20151203	MGI			PMID:24049736
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0009137	decreased brown fat lipid droplet number		IAGP		N	RGD:5509061	20151203	MGI			PMID:24049736
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141629
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200917	MGI			PMID:17360356
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20151203	MGI			PMID:24049736
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20151203	MGI			PMID:24049736
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20151203	MGI			PMID:24049736
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360356
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360356
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:17090215
1331978	Ppargc1b	peroxisome proliferative activated receptor, gamma, coactivator 1 beta	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:17360356
1331979	Tlr5	toll-like receptor 5	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891416
1331979	Tlr5	toll-like receptor 5	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891416
1331979	Tlr5	toll-like receptor 5	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891416
1331979	Tlr5	toll-like receptor 5	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16829963
1331979	Tlr5	toll-like receptor 5	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891416
1331979	Tlr5	toll-like receptor 5	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648852
1331979	Tlr5	toll-like receptor 5	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891416
1331979	Tlr5	toll-like receptor 5	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21458307
1331979	Tlr5	toll-like receptor 5	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891416
1331979	Tlr5	toll-like receptor 5	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16829963
1331979	Tlr5	toll-like receptor 5	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16829963
1331979	Tlr5	toll-like receptor 5	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20203013
1331979	Tlr5	toll-like receptor 5	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160324	MGI			PMID:25172014
1331979	Tlr5	toll-like receptor 5	gene	MP:0031342	increased circulating lipocalin 2 level		IAGP		N	RGD:5509061	20220120	MGI			PMID:20203013
1331981	Cacybp	calcyclin binding protein	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1331981	Cacybp	calcyclin binding protein	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413921
1331981	Cacybp	calcyclin binding protein	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413921
1331981	Cacybp	calcyclin binding protein	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413921
1331981	Cacybp	calcyclin binding protein	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413921
1331981	Cacybp	calcyclin binding protein	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1331981	Cacybp	calcyclin binding protein	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413921
1331981	Cacybp	calcyclin binding protein	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413921
1331981	Cacybp	calcyclin binding protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1331981	Cacybp	calcyclin binding protein	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16413921
1331981	Cacybp	calcyclin binding protein	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:16413921
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20111116	MGI			
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20111116	MGI			
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:21074052
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20250612	MGI			PMID:30327467
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20250612	MGI			PMID:30327467
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20240523	MGI			
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20240523	MGI			
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21074052
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20111116	MGI			
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0014538	decreased calcium level		IAGP		N	RGD:5509061	20250612	MGI			PMID:30327467
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:21074052
1331982	Cacna2d3	calcium channel, voltage-dependent, alpha2/delta subunit 3	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20250612	MGI			PMID:30327467
1331983	Kcnmb2	potassium large conductance calcium-activated channel, subfamily M, beta member 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151119	MGI			PMID:25267913
1331983	Kcnmb2	potassium large conductance calcium-activated channel, subfamily M, beta member 2	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20151119	MGI			PMID:25267913
1331983	Kcnmb2	potassium large conductance calcium-activated channel, subfamily M, beta member 2	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20151119	MGI			PMID:25267913
1331983	Kcnmb2	potassium large conductance calcium-activated channel, subfamily M, beta member 2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20151119	MGI			PMID:25267913
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:17189273
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15958588
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15958588
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:17189273
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17189273
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17189273
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17189273
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17189273
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20200310	MGI			PMID:17189273
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0014910	decreased hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:17189273
1331984	Sat1	spermidine/spermine N1-acetyl transferase 1	gene	MP:0014912	decreased fat cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:17189273
1331985	Timm13	translocase of inner mitochondrial membrane 13	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20190502	MGI			
1331985	Timm13	translocase of inner mitochondrial membrane 13	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1331985	Timm13	translocase of inner mitochondrial membrane 13	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20190502	MGI			
1331985	Timm13	translocase of inner mitochondrial membrane 13	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20190502	MGI			
1331985	Timm13	translocase of inner mitochondrial membrane 13	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20190502	MGI			
1331985	Timm13	translocase of inner mitochondrial membrane 13	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20190502	MGI			
1331985	Timm13	translocase of inner mitochondrial membrane 13	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20190502	MGI			
1331985	Timm13	translocase of inner mitochondrial membrane 13	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1331985	Timm13	translocase of inner mitochondrial membrane 13	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20210826	MGI			
1331986	Fam162a	family with sequence similarity 162, member A	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1331986	Fam162a	family with sequence similarity 162, member A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1331986	Fam162a	family with sequence similarity 162, member A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1331986	Fam162a	family with sequence similarity 162, member A	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1331986	Fam162a	family with sequence similarity 162, member A	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1331986	Fam162a	family with sequence similarity 162, member A	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20181227	MGI			
1331986	Fam162a	family with sequence similarity 162, member A	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1331986	Fam162a	family with sequence similarity 162, member A	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21669879
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566297
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19286635
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21669879
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566297
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18566297
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19286635
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21669879
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21669879
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21669879
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19286635
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19286635
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21669879
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21669879
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21669879
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19286635
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20170824	MGI			PMID:25605874
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20170824	MGI			PMID:25667419
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19286635
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0010163	hemolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19286635
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20170824	MGI			PMID:25605874
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20170824	MGI			PMID:25667419
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:25667419
1331987	Sgms2	sphingomyelin synthase 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:21669879
1331988	Dpysl5	dihydropyrimidinase-like 5	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289187
1331988	Dpysl5	dihydropyrimidinase-like 5	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289187
1331988	Dpysl5	dihydropyrimidinase-like 5	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289187
1331988	Dpysl5	dihydropyrimidinase-like 5	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21289187
1331988	Dpysl5	dihydropyrimidinase-like 5	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:21289187
1331989	Klb	klotho beta	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16075061
1331989	Klb	klotho beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16075061
1331989	Klb	klotho beta	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210520	MGI			
1331989	Klb	klotho beta	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210520	MGI			
1331989	Klb	klotho beta	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0003457	abnormal circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0003959	abnormal lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20210520	MGI			
1331989	Klb	klotho beta	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16075061
1331989	Klb	klotho beta	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0005457	abnormal percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0005667	abnormal circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0005675	small gallbladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:16075061
1331989	Klb	klotho beta	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220519	MGI			
1331989	Klb	klotho beta	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1331989	Klb	klotho beta	gene	MP:0012320	abnormal body fat mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0030967	abnormal circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:23209629
1331989	Klb	klotho beta	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:22958921
1331989	Klb	klotho beta	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:22958921
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20240627	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20201022	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20170105	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20200402	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200402	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20201231	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
1331990	Csnk1g3	casein kinase 1, gamma 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1331991	Tmem125	transmembrane protein 125	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20250508	MGI			
1331991	Tmem125	transmembrane protein 125	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1331991	Tmem125	transmembrane protein 125	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20250508	MGI			
1331991	Tmem125	transmembrane protein 125	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20250508	MGI			
1331991	Tmem125	transmembrane protein 125	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20250508	MGI			
1331991	Tmem125	transmembrane protein 125	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1331991	Tmem125	transmembrane protein 125	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20250508	MGI			
1331991	Tmem125	transmembrane protein 125	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20250508	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0000292	distended pericardium		IEA		N	RGD:5509061	20191128	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20181227	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20181227	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20181227	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0013214	decreased embryonic neuroepithelium primary cilium number		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1331996	Ppp1r35	protein phosphatase 1, regulatory subunit 35	gene	MP:0030538	abnormal notochordal plate morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:32628936
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0003169	abnormal scala media morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0004317	small vestibular saccule		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0004330	abnormal vestibular saccular macula morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0008307	short scala media		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0008308	small scala media		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0009259	abnormal vestibular saccule duct morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331997	Mctp1	multiple C2 domains, transmembrane 1	gene	MP:0013911	fused vestibular saccule and utricle		IAGP		N	RGD:5509061	20181220	MGI			PMID:30217595
1331998	Tmem86a	transmembrane protein 86A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1331998	Tmem86a	transmembrane protein 86A	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1331998	Tmem86a	transmembrane protein 86A	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1331998	Tmem86a	transmembrane protein 86A	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20231207	MGI			
1331998	Tmem86a	transmembrane protein 86A	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14716005
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14716005
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14716005
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14716005
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20200409	MGI			PMID:30976389
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14716005
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200409	MGI			PMID:30976389
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20200409	MGI			PMID:30976389
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14716005
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200409	MGI			PMID:30976389
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14716005
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14716005
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200409	MGI			PMID:30976389
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14716005
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16926188
1332001	Ss18l1	SS18, nBAF chromatin remodeling complex subunit like 1	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20200409	MGI			PMID:30976389
1332002	Dnase2b	deoxyribonuclease II beta	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1332002	Dnase2b	deoxyribonuclease II beta	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944971
1332002	Dnase2b	deoxyribonuclease II beta	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1332002	Dnase2b	deoxyribonuclease II beta	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944971
1332002	Dnase2b	deoxyribonuclease II beta	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944971
1332003	Vwce	von Willebrand factor C and EGF domains	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230119	MGI			
1332003	Vwce	von Willebrand factor C and EGF domains	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230119	MGI			
1332003	Vwce	von Willebrand factor C and EGF domains	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332004	Pgp	phosphoglycolate phosphatase	gene	MP:0011702	abnormal fibroblast proliferation		IAGP		N	RGD:5509061	20180426	MGI			PMID:27731369
1332005	Svop	SV2 related protein	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20201231	MGI			
1332005	Svop	SV2 related protein	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20201022	MGI			
1332005	Svop	SV2 related protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23894296
1332005	Svop	SV2 related protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23894296
1332005	Svop	SV2 related protein	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1332005	Svop	SV2 related protein	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1332005	Svop	SV2 related protein	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23894296
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584971
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584971
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366455
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366455
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366455
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141204	MGI			PMID:25102060
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001705	abnormal proximal-distal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141016	MGI			PMID:24361262
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24361262
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141016	MGI			PMID:24361262
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584971
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:25102060
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584971
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:35364055
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366455
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366455
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0003958	heart valve hyperplasia		IAGP		N	RGD:5509061	20231207	MGI			PMID:35364055
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584971
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141204	MGI			PMID:25102060
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366455
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584971
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0009594	abnormal corneocyte envelope morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366455
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0009603	absent keratohyalin granules		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366455
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0010197	abnormal lymphatic vessel endothelial cell morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24361262
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231207	MGI			PMID:35364055
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20231207	MGI			PMID:35364055
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20231207	MGI			PMID:35364055
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0010595	abnormal aortic valve cusp morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:35364055
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17584971
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141204	MGI			PMID:25102060
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0011233	abnormal vitamin A metabolism		IAGP		N	RGD:5509061	20231207	MGI			PMID:35364055
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0014106	delayed chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:15030763
1332006	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:15030763
1332007	Ccdc124	coiled-coil domain containing 124	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20170105	MGI			
1332007	Ccdc124	coiled-coil domain containing 124	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20170105	MGI			
1332007	Ccdc124	coiled-coil domain containing 124	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20170105	MGI			
1332007	Ccdc124	coiled-coil domain containing 124	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1332007	Ccdc124	coiled-coil domain containing 124	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1332007	Ccdc124	coiled-coil domain containing 124	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20170105	MGI			
1332007	Ccdc124	coiled-coil domain containing 124	gene	MP:0003641	small lung		IEA		N	RGD:5509061	20170105	MGI			
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20260122	MGI			PMID:39919786
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20260122	MGI			PMID:39919786
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20241121	MGI			
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260122	MGI			PMID:39919786
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20241121	MGI			
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20241121	MGI			
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:39919786
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20260402	MGI			
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:39919786
1332008	Dis3l	DIS3 like exosome 3'-5' exoribonuclease	gene	MP:0031739	impaired translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:39919786
1332010	Adipor1	adiponectin receptor 1	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20160421	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357764
1332010	Adipor1	adiponectin receptor 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357764
1332010	Adipor1	adiponectin receptor 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20201022	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357764
1332010	Adipor1	adiponectin receptor 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20181227	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20211021	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20180111	MGI			PMID:24531262
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357764
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357764
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005543	decreased cornea thickness		IEA		N	RGD:5509061	20181227	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357764
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20250508	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17268472
1332010	Adipor1	adiponectin receptor 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17327425
1332010	Adipor1	adiponectin receptor 1	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357764
1332010	Adipor1	adiponectin receptor 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0011019	abnormal adaptive thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:24531262
1332010	Adipor1	adiponectin receptor 1	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20180111	MGI			PMID:24531262
1332010	Adipor1	adiponectin receptor 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20181227	MGI			
1332010	Adipor1	adiponectin receptor 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20357764
1332010	Adipor1	adiponectin receptor 1	gene	MP:0014389	decreased skeletal muscle fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20250410	MGI			PMID:20357764
1332010	Adipor1	adiponectin receptor 1	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:24531262
1332010	Adipor1	adiponectin receptor 1	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:20357764
1332011	Amdhd2	amidohydrolase domain containing 2	gene	MP:0009453	enhanced contextual conditioning behavior		IEA		N	RGD:5509061	20250508	MGI			
1332011	Amdhd2	amidohydrolase domain containing 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220519	MGI			PMID:35229715
1332011	Amdhd2	amidohydrolase domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1332011	Amdhd2	amidohydrolase domain containing 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20250508	MGI			
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160114	MGI			PMID:9636176
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20160114	MGI			PMID:15755804
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20221215	MGI			
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0005083	abnormal biliary tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20160114	MGI			PMID:9636176
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20160114	MGI			PMID:9636176
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20160114	MGI			PMID:15755804
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0012183	decreased paraxial mesoderm size		IAGP		N	RGD:5509061	20160114	MGI			PMID:15755804
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0012183	decreased paraxial mesoderm size		IAGP		N	RGD:5509061	20160114	MGI			PMID:9636176
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0012254	absent intersomitic vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0012272	decreased axial mesoderm size		IAGP		N	RGD:5509061	20160114	MGI			PMID:15755804
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0012498	abnormal cardiogenic plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490058
1332013	Poglut1	protein O-glucosyltransferase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220428	MGI			
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:20582322
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:31867855
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20201210	MGI			PMID:31867855
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31867855
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20201210	MGI			PMID:31867855
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0008853	decreased abdominal adipose tissue amount		IEA		N	RGD:5509061	20141003	MGI			
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20201210	MGI			PMID:31867855
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20141003	MGI			
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201210	MGI			PMID:31867855
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0014639	decreased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:20582322
1332015	Tmub1	transmembrane and ubiquitin-like domain containing 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:20582322
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20220630	MGI			PMID:34302166
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:26787558
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20220630	MGI			PMID:34302166
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20180607	MGI			PMID:26787558
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20220630	MGI			PMID:34302166
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20180607	MGI			PMID:26787558
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20220630	MGI			PMID:34302166
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20220630	MGI			PMID:34302166
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20180607	MGI			PMID:26787558
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:34302166
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221027	MGI			PMID:33446878
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220630	MGI			PMID:34302166
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221027	MGI			PMID:33446878
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180607	MGI			PMID:26787558
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180607	MGI			PMID:26787558
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220630	MGI			PMID:34302166
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0012746	abnormal neural crest cell delamination		IAGP		N	RGD:5509061	20180607	MGI			PMID:26787558
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20180607	MGI			PMID:26787558
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:34302166
1332016	Specc1l	sperm antigen with calponin homology and coiled-coil domains 1-like	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20221027	MGI			PMID:33446878
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17318259
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17318259
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023421
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023421
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023421
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17318259
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17318259
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023421
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0005074	impaired granulocyte bactericidal activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17318259
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023421
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023421
1332017	G6pc3	glucose 6 phosphatase, catalytic, 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17318259
1332018	Kng1	kininogen 1	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18000168
1332018	Kng1	kininogen 1	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20200924	MGI			PMID:18000168
1332018	Kng1	kininogen 1	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200924	MGI			PMID:18000168
1332019	Lrr1	leucine rich repeat protein 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20181227	MGI			
1332019	Lrr1	leucine rich repeat protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332019	Lrr1	leucine rich repeat protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20170105	MGI			
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20170105	MGI			
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20170105	MGI			
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0010767	abnormal female meiosis I arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0013236	ovary degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1332022	Terb1	telomere repeat binding bouquet formation protein 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:24413433
1332023	Tmem79	transmembrane protein 79	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20141003	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0000402	abnormal zigzag hair morphology		IEA		N	RGD:5509061	20120105	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0000403	increased curvature of zigzag hairs		IEA		N	RGD:5509061	20120105	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0000411	shiny fur		IEA		N	RGD:5509061	20120105	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0000416	sparse hair		IEA		N	RGD:5509061	20120105	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0000427	abnormal hair cycle		IEA		N	RGD:5509061	20141003	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0001191	abnormal skin condition		IEA		N	RGD:5509061	20120105	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24060273
1332023	Tmem79	transmembrane protein 79	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24060273
1332023	Tmem79	transmembrane protein 79	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:24060273
1332023	Tmem79	transmembrane protein 79	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24060273
1332023	Tmem79	transmembrane protein 79	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0002073	abnormal hair growth		IEA		N	RGD:5509061	20141003	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20120105	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:24060273
1332023	Tmem79	transmembrane protein 79	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0003809	abnormal hair shaft morphology		IEA		N	RGD:5509061	20141003	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0003846	matted coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:24060273
1332023	Tmem79	transmembrane protein 79	gene	MP:0003846	matted coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0005409	darkened coat color		IEA		N	RGD:5509061	20141003	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0009594	abnormal corneocyte envelope morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0009801	abnormal hair cortex keratinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24084074
1332023	Tmem79	transmembrane protein 79	gene	MP:0010686	abnormal hair follicle matrix region morphology		IEA		N	RGD:5509061	20141003	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20170105	MGI			
1332023	Tmem79	transmembrane protein 79	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1332024	Pla1a	phospholipase A1 member A	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1332024	Pla1a	phospholipase A1 member A	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20230601	MGI			PMID:35955693
1332024	Pla1a	phospholipase A1 member A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230601	MGI			PMID:35955693
1332024	Pla1a	phospholipase A1 member A	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20230601	MGI			PMID:35955693
1332024	Pla1a	phospholipase A1 member A	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20230601	MGI			PMID:35955693
1332024	Pla1a	phospholipase A1 member A	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20230601	MGI			PMID:35955693
1332024	Pla1a	phospholipase A1 member A	gene	MP:0012573	decreased susceptibility to chemically induced skin inflammation		IAGP		N	RGD:5509061	20230601	MGI			PMID:35955693
1332026	Trim23	tripartite motif-containing 23	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20240516	MGI			PMID:33957127
1332026	Trim23	tripartite motif-containing 23	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20240516	MGI			PMID:33957127
1332029	Gpm6a	glycoprotein m6a	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21714103
1332029	Gpm6a	glycoprotein m6a	gene	MP:0005458	increased percent body fat/body weight		IEA		N	RGD:5509061	20111116	MGI			
1332032	Il24	interleukin 24	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20170105	MGI			
1332032	Il24	interleukin 24	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1332032	Il24	interleukin 24	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1332032	Il24	interleukin 24	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1332034	Rab15	RAB15, member RAS oncogene family	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20170105	MGI			
1332034	Rab15	RAB15, member RAS oncogene family	gene	MP:0002727	decreased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19583954
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19583954
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19583954
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133702
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133702
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0005439	decreased glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19583954
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20200102	MGI			PMID:20133702
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0020103	decreased hepatic glucose production		IAGP		N	RGD:5509061	20200102	MGI			PMID:20133702
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:24898145
1332035	Crtc2	CREB regulated transcription coactivator 2	gene	MP:0030973	impaired gluconeogenesis		IAGP		N	RGD:5509061	20200102	MGI			PMID:20133702
1332036	Zfp57	zinc finger protein 57	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854139
1332036	Zfp57	zinc finger protein 57	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854139
1332036	Zfp57	zinc finger protein 57	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854139
1332036	Zfp57	zinc finger protein 57	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854139
1332038	Atp6v1f	ATPase, H+ transporting, lysosomal V1 subunit F	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1332038	Atp6v1f	ATPase, H+ transporting, lysosomal V1 subunit F	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1332038	Atp6v1f	ATPase, H+ transporting, lysosomal V1 subunit F	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354928
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:22049418
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:17099708
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:23792428
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:15987683
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15987683
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:14664815
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:15987683
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354928
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:15987683
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:23792428
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:23792428
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20200310	MGI			PMID:14664815
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354928
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385378
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15987683
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354928
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14664815
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:11224535
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:11406613
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15080893
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22049418
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20200310	MGI			PMID:14664815
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354928
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354928
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354928
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22049418
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385378
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20200310	MGI			PMID:15987683
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15987683
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17099708
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:17099708
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385378
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23792428
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15987683
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15824102
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354928
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354928
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385378
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0008486	decreased muscle spindle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23792428
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385378
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385378
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385378
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:17099708
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15987683
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0011619	abnormal dishabituation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385378
1332039	Bace1	beta-site APP cleaving enzyme 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:15987683
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160804	MGI			
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0006428	ectopic Sertoli cells		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20160804	MGI			
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994007
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0020355	abnormal Sertoli cell barrier morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0020356	abnormal Sertoli cell barrier function		IAGP		N	RGD:5509061	20220616	MGI			PMID:35440090
1332040	Uhrf1	ubiquitin-like, containing PHD and RING finger domains, 1	gene	MP:0031406	decreased Sertoli cell proliferation		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440090
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160421	MGI			
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636852
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20160421	MGI			
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:21636852
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636852
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20211021	MGI			
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1332043	Ndrg4	N-myc downstream regulated gene 4	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21636852
1332044	Cxcl9	C-X-C motif chemokine ligand 9	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20181227	MGI			
1332044	Cxcl9	C-X-C motif chemokine ligand 9	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1332044	Cxcl9	C-X-C motif chemokine ligand 9	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12133969
1332044	Cxcl9	C-X-C motif chemokine ligand 9	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296171
1332044	Cxcl9	C-X-C motif chemokine ligand 9	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12133969
1332044	Cxcl9	C-X-C motif chemokine ligand 9	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296171
1332044	Cxcl9	C-X-C motif chemokine ligand 9	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1332044	Cxcl9	C-X-C motif chemokine ligand 9	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1332044	Cxcl9	C-X-C motif chemokine ligand 9	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0000925	abnormal floor plate morphology		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0000928	incomplete rostral neuropore closure		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0000932	absent notochord		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0003119	abnormal digestive system development		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0003400	kinked neural tube		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0004180	failure of initiation of embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0012270	cardiac edema		IEA		N	RGD:5509061	20251211	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1332045	Tedc2	tubulin epsilon and delta complex 2	gene	MP:0014134	abnormal embryo morphology		IEA		N	RGD:5509061	20251211	MGI			
1332046	Ints7	integrator complex subunit 7	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1332046	Ints7	integrator complex subunit 7	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201231	MGI			
1332046	Ints7	integrator complex subunit 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332046	Ints7	integrator complex subunit 7	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1332048	Abat	4-aminobutyrate aminotransferase	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
1332048	Abat	4-aminobutyrate aminotransferase	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
1332048	Abat	4-aminobutyrate aminotransferase	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
1332048	Abat	4-aminobutyrate aminotransferase	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
1332048	Abat	4-aminobutyrate aminotransferase	gene	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
1332048	Abat	4-aminobutyrate aminotransferase	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IAGP		N	RGD:5509061	20240606	MGI			PMID:36192601
1332048	Abat	4-aminobutyrate aminotransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332049	Dlgap2	DLG associated protein 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1332049	Dlgap2	DLG associated protein 2	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20180809	MGI			PMID:25071926
1332049	Dlgap2	DLG associated protein 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20180809	MGI			PMID:25071926
1332049	Dlgap2	DLG associated protein 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1332049	Dlgap2	DLG associated protein 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20180809	MGI			PMID:25071926
1332049	Dlgap2	DLG associated protein 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20180809	MGI			PMID:25071926
1332049	Dlgap2	DLG associated protein 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25071926
1332049	Dlgap2	DLG associated protein 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1332049	Dlgap2	DLG associated protein 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1332049	Dlgap2	DLG associated protein 2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20180809	MGI			PMID:25071926
1332049	Dlgap2	DLG associated protein 2	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25071926
1332049	Dlgap2	DLG associated protein 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1332049	Dlgap2	DLG associated protein 2	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20180809	MGI			PMID:25071926
1332049	Dlgap2	DLG associated protein 2	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25071926
1332050	Fgd4	FYVE, RhoGEF and PH domain containing 4	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1332050	Fgd4	FYVE, RhoGEF and PH domain containing 4	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23171661
1332050	Fgd4	FYVE, RhoGEF and PH domain containing 4	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23171661
1332050	Fgd4	FYVE, RhoGEF and PH domain containing 4	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23171661
1332050	Fgd4	FYVE, RhoGEF and PH domain containing 4	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23171661
1332050	Fgd4	FYVE, RhoGEF and PH domain containing 4	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23171661
1332050	Fgd4	FYVE, RhoGEF and PH domain containing 4	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23171661
1332050	Fgd4	FYVE, RhoGEF and PH domain containing 4	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23171661
1332052	Qrich1	glutamine-rich 1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20170209	MGI			
1332052	Qrich1	glutamine-rich 1	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20170209	MGI			
1332052	Qrich1	glutamine-rich 1	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170209	MGI			
1332052	Qrich1	glutamine-rich 1	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20170209	MGI			
1332052	Qrich1	glutamine-rich 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260122	MGI			PMID:40608935
1332052	Qrich1	glutamine-rich 1	gene	MP:0004056	abnormal myocardium compact layer morphology		IEA		N	RGD:5509061	20170209	MGI			
1332052	Qrich1	glutamine-rich 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20260122	MGI			PMID:40608935
1332052	Qrich1	glutamine-rich 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20170209	MGI			
1332052	Qrich1	glutamine-rich 1	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20170209	MGI			
1332052	Qrich1	glutamine-rich 1	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170209	MGI			
1332052	Qrich1	glutamine-rich 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:40608935
1332052	Qrich1	glutamine-rich 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:40608935
1332052	Qrich1	glutamine-rich 1	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20260122	MGI			PMID:40608935
1332052	Qrich1	glutamine-rich 1	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20170209	MGI			
1332052	Qrich1	glutamine-rich 1	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20260122	MGI			PMID:40608935
1332053	Chn1	chimerin 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17719550
1332053	Chn1	chimerin 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
1332053	Chn1	chimerin 1	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1332053	Chn1	chimerin 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17719550
1332053	Chn1	chimerin 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:24623763
1332053	Chn1	chimerin 1	gene	MP:0001070	abnormal abducens nerve morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
1332053	Chn1	chimerin 1	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1332053	Chn1	chimerin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17719550
1332053	Chn1	chimerin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785182
1332053	Chn1	chimerin 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1332053	Chn1	chimerin 1	gene	MP:0001396	unidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785182
1332053	Chn1	chimerin 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1332053	Chn1	chimerin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17719550
1332053	Chn1	chimerin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785182
1332053	Chn1	chimerin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1332053	Chn1	chimerin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20150219	MGI			PMID:24623763
1332053	Chn1	chimerin 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1332053	Chn1	chimerin 1	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1332053	Chn1	chimerin 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
1332053	Chn1	chimerin 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20150219	MGI			
1332053	Chn1	chimerin 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785182
1332053	Chn1	chimerin 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
1332053	Chn1	chimerin 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17719550
1332053	Chn1	chimerin 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210520	MGI			
1332053	Chn1	chimerin 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20231207	MGI			
1332053	Chn1	chimerin 1	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20160421	MGI			
1332053	Chn1	chimerin 1	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785182
1332053	Chn1	chimerin 1	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17719550
1332053	Chn1	chimerin 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1332053	Chn1	chimerin 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1332053	Chn1	chimerin 1	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20150219	MGI			PMID:24623763
1332053	Chn1	chimerin 1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785182
1332053	Chn1	chimerin 1	gene	MP:0003880	abnormal central pattern generator function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785182
1332053	Chn1	chimerin 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1332053	Chn1	chimerin 1	gene	MP:0004100	abnormal spinal cord interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1332053	Chn1	chimerin 1	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1332053	Chn1	chimerin 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1332053	Chn1	chimerin 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1332053	Chn1	chimerin 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
1332053	Chn1	chimerin 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1332053	Chn1	chimerin 1	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
1332053	Chn1	chimerin 1	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17719550
1332053	Chn1	chimerin 1	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1332053	Chn1	chimerin 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1332053	Chn1	chimerin 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332053	Chn1	chimerin 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785182
1332053	Chn1	chimerin 1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20201022	MGI			
1332055	Slc4a9	solute carrier family 4, sodium bicarbonate cotransporter, member 9	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170027
1332055	Slc4a9	solute carrier family 4, sodium bicarbonate cotransporter, member 9	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23610411
1332056	Hnrnpr	heterogeneous nuclear ribonucleoprotein R	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20240425	MGI			PMID:34850154
1332056	Hnrnpr	heterogeneous nuclear ribonucleoprotein R	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:34850154
1332057	Rtcb	RNA 2',3'-cyclic phosphate and 5'-OH ligase	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20230330	MGI			PMID:36178098
1332057	Rtcb	RNA 2',3'-cyclic phosphate and 5'-OH ligase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20151008	MGI			PMID:25378478
1332057	Rtcb	RNA 2',3'-cyclic phosphate and 5'-OH ligase	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20230330	MGI			PMID:36178098
1332057	Rtcb	RNA 2',3'-cyclic phosphate and 5'-OH ligase	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:25378478
1332057	Rtcb	RNA 2',3'-cyclic phosphate and 5'-OH ligase	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20151008	MGI			PMID:25378478
1332057	Rtcb	RNA 2',3'-cyclic phosphate and 5'-OH ligase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20151008	MGI			PMID:25378478
1332057	Rtcb	RNA 2',3'-cyclic phosphate and 5'-OH ligase	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20230330	MGI			PMID:36178098
1332057	Rtcb	RNA 2',3'-cyclic phosphate and 5'-OH ligase	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20230330	MGI			PMID:36178098
1332057	Rtcb	RNA 2',3'-cyclic phosphate and 5'-OH ligase	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20230330	MGI			PMID:36178098
1332058	Bod1	biorientation of chromosomes in cell division 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1332058	Bod1	biorientation of chromosomes in cell division 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1332058	Bod1	biorientation of chromosomes in cell division 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1332058	Bod1	biorientation of chromosomes in cell division 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1332058	Bod1	biorientation of chromosomes in cell division 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20141003	MGI			
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467576
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20141003	MGI			
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0002698	abnormal sclera morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23839944
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467576
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467576
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0004185	abnormal adipocyte glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:23839944
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0005098	abnormal optic choroid morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23839944
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23839944
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0006237	abnormal choroid vasculature morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467576
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23839944
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467576
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467576
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0010192	abnormal retina melanin granule morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467576
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0011232	abnormal vitamin A level		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0011233	abnormal vitamin A metabolism		IAGP		N	RGD:5509061	20141030	MGI			PMID:24391722
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0011233	abnormal vitamin A metabolism		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0011234	abnormal retinol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22467576
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0011996	abnormal retina inner nuclear layer thickness		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20150910	MGI			PMID:24852372
1332061	Stra6	stimulated by retinoic acid gene 6	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:24852372
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483953
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23894296
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10624962
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483953
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10624962
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0002917	decreased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:10624962
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19381277
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11483953
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19381277
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10624962
1332062	Sv2b	synaptic vesicle glycoprotein 2b	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23894296
1332063	Sap130	Sin3A associated protein	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20200402	MGI			
1332063	Sap130	Sin3A associated protein	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20170831	MGI			PMID:28530678
1332063	Sap130	Sin3A associated protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21937600
1332063	Sap130	Sin3A associated protein	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20170831	MGI			PMID:28530678
1332063	Sap130	Sin3A associated protein	gene	MP:0010446	heart left ventricle hypoplasia		IAGP		N	RGD:5509061	20170824	MGI			PMID:28530678
1332063	Sap130	Sin3A associated protein	gene	MP:0010463	aorta stenosis		IAGP		N	RGD:5509061	20170824	MGI			PMID:28530678
1332063	Sap130	Sin3A associated protein	gene	MP:0010541	aorta hypoplasia		IAGP		N	RGD:5509061	20170831	MGI			PMID:28530678
1332063	Sap130	Sin3A associated protein	gene	MP:0010580	decreased heart left ventricle size		IAGP		N	RGD:5509061	20170831	MGI			PMID:28530678
1332063	Sap130	Sin3A associated protein	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20170824	MGI			PMID:28530678
1332063	Sap130	Sin3A associated protein	gene	MP:0011939	increased food intake		IEA		N	RGD:5509061	20210128	MGI			
1332063	Sap130	Sin3A associated protein	gene	MP:0031523	mitral valve hypoplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:28530678
1332064	Padi3	peptidyl arginine deiminase, type III	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27866708
1332064	Padi3	peptidyl arginine deiminase, type III	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1332064	Padi3	peptidyl arginine deiminase, type III	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27866708
1332064	Padi3	peptidyl arginine deiminase, type III	gene	MP:0002832	coarse hair		IAGP		N	RGD:5509061	20170119	MGI			PMID:27866708
1332064	Padi3	peptidyl arginine deiminase, type III	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27866708
1332064	Padi3	peptidyl arginine deiminase, type III	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1332064	Padi3	peptidyl arginine deiminase, type III	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1332064	Padi3	peptidyl arginine deiminase, type III	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1332064	Padi3	peptidyl arginine deiminase, type III	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20170119	MGI			PMID:27866708
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210805	MGI			
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210805	MGI			
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20210805	MGI			
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210805	MGI			
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0003488	decreased channel response intensity		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210805	MGI			
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0009148	pancreas necrosis		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0014121	increased pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332067	Kcnh6	potassium voltage-gated channel, subfamily H (eag-related), member 6	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20200416	MGI			PMID:30590050
1332070	Ybx2	Y box protein 2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0002679	abnormal corpus luteum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0003696	abnormal zona pellucida morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:15824319
1332070	Ybx2	Y box protein 2	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:15824319
1332071	Rbm48	RNA binding motif protein 48	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1332071	Rbm48	RNA binding motif protein 48	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689692
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0002798	abnormal active avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332072	Ntan1	N-terminal Asn amidase	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10805755
1332073	Pdap1	PDGFA associated protein 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1332073	Pdap1	PDGFA associated protein 1	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1332073	Pdap1	PDGFA associated protein 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1332073	Pdap1	PDGFA associated protein 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1332073	Pdap1	PDGFA associated protein 1	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1332073	Pdap1	PDGFA associated protein 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1332073	Pdap1	PDGFA associated protein 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20210708	MGI			PMID:32609329
1332074	Cnpy4	canopy FGF signaling regulator 4	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1332074	Cnpy4	canopy FGF signaling regulator 4	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20230601	MGI			
1332074	Cnpy4	canopy FGF signaling regulator 4	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1332074	Cnpy4	canopy FGF signaling regulator 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1332074	Cnpy4	canopy FGF signaling regulator 4	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230601	MGI			
1332076	Slain2	SLAIN motif family, member 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1332076	Slain2	SLAIN motif family, member 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220811	MGI			
1332076	Slain2	SLAIN motif family, member 2	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20220811	MGI			
1332076	Slain2	SLAIN motif family, member 2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1332076	Slain2	SLAIN motif family, member 2	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1332076	Slain2	SLAIN motif family, member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1332077	Mlec	malectin	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20150108	MGI			
1332077	Mlec	malectin	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1332077	Mlec	malectin	gene	MP:0005477	increased circulating thyroxine level		IEA		N	RGD:5509061	20210128	MGI			
1332077	Mlec	malectin	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1332079	Cwh43	cell wall biogenesis 43 C-terminal homolog	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:33459505
1332079	Cwh43	cell wall biogenesis 43 C-terminal homolog	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1332079	Cwh43	cell wall biogenesis 43 C-terminal homolog	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20230309	MGI			PMID:33459505
1332079	Cwh43	cell wall biogenesis 43 C-terminal homolog	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20230309	MGI			PMID:33459505
1332079	Cwh43	cell wall biogenesis 43 C-terminal homolog	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20230309	MGI			PMID:33459505
1332079	Cwh43	cell wall biogenesis 43 C-terminal homolog	gene	MP:0010152	abnormal brain ependyma morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:33459505
1332079	Cwh43	cell wall biogenesis 43 C-terminal homolog	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20230309	MGI			PMID:33459505
1332079	Cwh43	cell wall biogenesis 43 C-terminal homolog	gene	MP:0030966	decreased brain ependyma motile cilium number		IAGP		N	RGD:5509061	20230309	MGI			PMID:33459505
1332080	Egflam	EGF-like, fibronectin type III and laminin G domains	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641643
1332080	Egflam	EGF-like, fibronectin type III and laminin G domains	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641643
1332080	Egflam	EGF-like, fibronectin type III and laminin G domains	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641643
1332080	Egflam	EGF-like, fibronectin type III and laminin G domains	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641643
1332080	Egflam	EGF-like, fibronectin type III and laminin G domains	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641643
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201022	MGI			
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20160407	MGI			PMID:26728762
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20160407	MGI			PMID:26728762
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220428	MGI			
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20160407	MGI			PMID:26728762
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484369
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20160407	MGI			PMID:26728762
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20160407	MGI			PMID:26728762
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002915	abnormal synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20160407	MGI			PMID:26728762
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0006299	abnormal latent inhibition of conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0006300	abnormal entorhinal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20141003	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0012347	low sweet preference		IAGP		N	RGD:5509061	20150917	MGI			PMID:24908665
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:17481393
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:21903668
1332081	Disc1	disrupted in schizophrenia 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:26728762
1332082	4930558K02Rik	RIKEN cDNA 4930558K02 gene	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1332083	Actl9	actin-like 9	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20210429	MGI			PMID:33626338
1332083	Actl9	actin-like 9	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:33626338
1332083	Actl9	actin-like 9	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:33626338
1332083	Actl9	actin-like 9	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20210429	MGI			PMID:33626338
1332083	Actl9	actin-like 9	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220303	MGI			PMID:33626338
1332083	Actl9	actin-like 9	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20220303	MGI			PMID:33626338
1332084	Slco1a5	solute carrier organic anion transporter family, member 1a5	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IEA		N	RGD:5509061	20111116	MGI			
1332084	Slco1a5	solute carrier organic anion transporter family, member 1a5	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20111116	MGI			
1332085	Ring1	ring finger protein 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060235
1332085	Ring1	ring finger protein 1	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060235
1332085	Ring1	ring finger protein 1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060235
1332085	Ring1	ring finger protein 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060235
1332085	Ring1	ring finger protein 1	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060235
1332086	Khsrp	KH-type splicing regulatory protein	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1332086	Khsrp	KH-type splicing regulatory protein	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230601	MGI			
1332086	Khsrp	KH-type splicing regulatory protein	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690298
1332086	Khsrp	KH-type splicing regulatory protein	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20230601	MGI			
1332086	Khsrp	KH-type splicing regulatory protein	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1332086	Khsrp	KH-type splicing regulatory protein	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230601	MGI			
1332086	Khsrp	KH-type splicing regulatory protein	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:21690298
1332086	Khsrp	KH-type splicing regulatory protein	gene	MP:0031025	decreased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:21690298
1332087	Pa2g4	proliferation-associated 2G4	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19094237
1332087	Pa2g4	proliferation-associated 2G4	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19094237
1332087	Pa2g4	proliferation-associated 2G4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19094237
1332087	Pa2g4	proliferation-associated 2G4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19094237
1332087	Pa2g4	proliferation-associated 2G4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19094237
1332087	Pa2g4	proliferation-associated 2G4	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1332087	Pa2g4	proliferation-associated 2G4	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19094237
1332088	Sorbs3	sorbin and SH3 domain containing 3	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20361963
1332088	Sorbs3	sorbin and SH3 domain containing 3	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20361963
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220811	MGI			PMID:35574006
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20201029	MGI			PMID:31365862
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220811	MGI			PMID:35574006
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0002139	abnormal hepatobiliary system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808103
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611695
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0003095	abnormal cornea stroma development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0004054	abnormal periocular mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611695
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611695
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:35574006
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0005195	abnormal posterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611695
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20220811	MGI			PMID:35574006
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0006162	thick eyelids		IAGP		N	RGD:5509061	20141225	MGI			PMID:16611695
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0008881	absent Harderian gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0009742	increased cornea stroma thickness		IAGP		N	RGD:5509061	20141225	MGI			PMID:16611695
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0010706	ventral rotation of lens		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0010707	decreased ventral retina size		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0010708	absent iris stroma		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0010710	absent sclera		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611695
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0011964	increased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16611695
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0013744	abnormal conjunctival sac morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0030326	decreased periocular mesenchyme apoptosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:16207763
1332089	Aldh1a1	aldehyde dehydrogenase family 1, subfamily A1	gene	MP:0030326	decreased periocular mesenchyme apoptosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:16611695
1332090	Ripor1	RHO family interacting cell polarization regulator 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1332092	Cd200	CD200 molecule	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20200310	MGI			
1332092	Cd200	CD200 molecule	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0004821	increased susceptibility to experimental autoimmune uveoretinitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12414514
1332092	Cd200	CD200 molecule	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:12414514
1332092	Cd200	CD200 molecule	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12414514
1332092	Cd200	CD200 molecule	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:11099416
1332092	Cd200	CD200 molecule	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15611236
1332092	Cd200	CD200 molecule	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1332093	Carhsp1	calcium regulated heat stable protein 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1332093	Carhsp1	calcium regulated heat stable protein 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1332093	Carhsp1	calcium regulated heat stable protein 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1332095	Vps13d	vacuolar protein sorting 13D	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1332095	Vps13d	vacuolar protein sorting 13D	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200402	MGI			
1332095	Vps13d	vacuolar protein sorting 13D	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1332096	Crygf	crystallin, gamma F	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:3352637
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:24274065
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0001775	abnormal selenium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24274065
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24274065
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0005468	abnormal thyroid hormone level		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0005470	increased thyroxine level		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0005473	decreased triiodothyronine level		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0005646	abnormal pituitary gland physiology		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20160804	MGI			
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190801	MGI			PMID:29029094
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24274065
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24274065
1332097	Secisbp2	SECIS binding protein 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24274065
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0000494	abnormal cecum morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0003288	intestinal edema		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0003332	liver abscess		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0004918	abnormal negative T cell selection		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0005002	abnormal T cell clonal deletion		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20201022	MGI			
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0008895	abnormal intraepithelial T cell number		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20250724	MGI			PMID:39158947
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201022	MGI			
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0013793	abnormal large intestine goblet cell morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0014495	increased circulating chemokine level		IAGP		N	RGD:5509061	20260305	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0031113	pulmonary parenchymal consolidation		IAGP		N	RGD:5509061	20200806	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0031220	increased circulating CXCL10 level		IAGP		N	RGD:5509061	20210204	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0031251	increased circulating CCL3 level		IAGP		N	RGD:5509061	20260305	MGI			PMID:31285585
1332100	Cyrib	CYFIP related Rac1 interactor B	gene	MP:0031702	increased circulating CCL4 level		IAGP		N	RGD:5509061	20260312	MGI			PMID:31285585
1332101	Gsdmd	gasdermin D	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18693275
1332101	Gsdmd	gasdermin D	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20180111	MGI			PMID:28636595
1332101	Gsdmd	gasdermin D	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20160630	MGI			PMID:26375003
1332101	Gsdmd	gasdermin D	gene	MP:0011073	abnormal macrophage apoptosis		IAGP		N	RGD:5509061	20160630	MGI			PMID:26375003
1332101	Gsdmd	gasdermin D	gene	MP:0020186	abnormal susceptibility to bacterial infection		IEA		N	RGD:5509061	20180920	MGI			
1332101	Gsdmd	gasdermin D	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:28636595
1332106	Ndnf	neuron-derived neurotrophic factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26727548
1332106	Ndnf	neuron-derived neurotrophic factor	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20220421	MGI			PMID:35051783
1332106	Ndnf	neuron-derived neurotrophic factor	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20220421	MGI			PMID:35051783
1332106	Ndnf	neuron-derived neurotrophic factor	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20220421	MGI			PMID:35051783
1332107	Gsc	goosecoid homeobox	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000098	abnormal vomer bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0000098	abnormal vomer bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0000100	abnormal ethmoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10512191
1332107	Gsc	goosecoid homeobox	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1332107	Gsc	goosecoid homeobox	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1332107	Gsc	goosecoid homeobox	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1332107	Gsc	goosecoid homeobox	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0002234	abnormal pharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0002238	abnormal nasal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0003110	absent malleus processus brevis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10512191
1332107	Gsc	goosecoid homeobox	gene	MP:0003110	absent malleus processus brevis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0004234	abnormal masticatory muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0004450	presphenoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0004456	small pterygoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0004459	small alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0004475	palatine bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0004554	small pharynx		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0004627	abnormal trochanter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0004689	small ischium		IAGP		N	RGD:5509061	20181011	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0004873	absent turbinates		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10512191
1332107	Gsc	goosecoid homeobox	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0006018	abnormal tympanic membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0006019	absent tympanic membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:10512191
1332107	Gsc	goosecoid homeobox	gene	MP:0006019	absent tympanic membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10512191
1332107	Gsc	goosecoid homeobox	gene	MP:0006033	abnormal external auditory canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0006344	small second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0008376	small malleus manubrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0008376	small malleus manubrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0008378	small malleus processus brevis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0009575	abnormal pubic symphysis morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0009707	absent external auditory canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:10512191
1332107	Gsc	goosecoid homeobox	gene	MP:0009707	absent external auditory canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20171123	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0010355	abnormal first pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0010549	absent dorsal mesocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0012069	abnormal horizontal basal cell of olfactory epithelium morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127040
1332107	Gsc	goosecoid homeobox	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0012263	decreased hindbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9226455
1332107	Gsc	goosecoid homeobox	gene	MP:0030059	absent ethmoturbinates		IAGP		N	RGD:5509061	20170921	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0030154	abnormal tympanic cavity morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:10512191
1332107	Gsc	goosecoid homeobox	gene	MP:0030187	abnormal epitympanic recess morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:10512191
1332107	Gsc	goosecoid homeobox	gene	MP:0030208	abnormal intrinsic tongue muscle morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0030209	abnormal extrinsic tongue muscle morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0030210	abnormal genioglossus muscle morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:7555726
1332107	Gsc	goosecoid homeobox	gene	MP:0030266	small vomer bone		IAGP		N	RGD:5509061	20171026	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0030266	small vomer bone		IAGP		N	RGD:5509061	20171026	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0030283	small mandibular coronoid process		IAGP		N	RGD:5509061	20171102	MGI			PMID:7555718
1332107	Gsc	goosecoid homeobox	gene	MP:0030305	small cribriform plate		IAGP		N	RGD:5509061	20171109	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0030788	abnormal femur head morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0030816	abnormal shoulder joint morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0030828	abnormal obturator foramen morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0030829	abnormal hip joint morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0030830	abnormal acetabulum morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0030831	abnormal glenoid fossa morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:9533949
1332107	Gsc	goosecoid homeobox	gene	MP:0030832	abnormal scapular coracoid process morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:9533949
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0012338	decreased bile salt level		IAGP		N	RGD:5509061	20240613	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0014479	decreased feces bile salt level		IAGP		N	RGD:5509061	20240704	MGI			PMID:31645370
1332108	Cyp2a12	cytochrome P450, family 2, subfamily a, polypeptide 12	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:31645370
1332109	Cpsf7	cleavage and polyadenylation specific factor 7	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20190502	MGI			
1332109	Cpsf7	cleavage and polyadenylation specific factor 7	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1332109	Cpsf7	cleavage and polyadenylation specific factor 7	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1332110	Aacs	acetoacetyl-CoA synthetase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1332113	Pamr1	peptidase domain containing associated with muscle regeneration 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1332113	Pamr1	peptidase domain containing associated with muscle regeneration 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1332113	Pamr1	peptidase domain containing associated with muscle regeneration 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1332113	Pamr1	peptidase domain containing associated with muscle regeneration 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1332113	Pamr1	peptidase domain containing associated with muscle regeneration 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1332113	Pamr1	peptidase domain containing associated with muscle regeneration 1	gene	MP:0010896	decreased lung compliance		IEA		N	RGD:5509061	20250508	MGI			
1332113	Pamr1	peptidase domain containing associated with muscle regeneration 1	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20250508	MGI			
1332113	Pamr1	peptidase domain containing associated with muscle regeneration 1	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20250508	MGI			
1332113	Pamr1	peptidase domain containing associated with muscle regeneration 1	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20250508	MGI			
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19324999
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:17030627
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:17030627
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:17030627
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:17379411
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20200310	MGI			PMID:19324999
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20200310	MGI			PMID:19584200
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:19324999
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:17030627
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:19584200
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19324999
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19584200
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19324999
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19324999
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:19324999
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:17379411
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:19584200
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:19324999
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:19324999
1332115	Nmur2	neuromedin U receptor 2	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:17030627
1332116	Pyroxd1	pyridine nucleotide-disulphide oxidoreductase domain 1	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20161201	MGI			
1332116	Pyroxd1	pyridine nucleotide-disulphide oxidoreductase domain 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20190502	MGI			
1332116	Pyroxd1	pyridine nucleotide-disulphide oxidoreductase domain 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332116	Pyroxd1	pyridine nucleotide-disulphide oxidoreductase domain 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1332117	Sema3d	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D	gene	MP:0002726	abnormal pulmonary vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23685842
1332117	Sema3d	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23685842
1332117	Sema3d	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D	gene	MP:0008727	increased heart right atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23685842
1332117	Sema3d	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23685842
1332117	Sema3d	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23685842
1332117	Sema3d	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332117	Sema3d	sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D	gene	MP:0031129	left-to-right shunt		IAGP		N	RGD:5509061	20201015	MGI			PMID:23685842
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056871
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056871
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0002905	decreased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056871
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056871
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0010110	abnormal renal phosphate reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056871
1332118	Slc34a3	solute carrier family 34 (sodium phosphate), member 3	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570882
1332119	Siae	sialic acid acetylesterase	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0008169	increased B-1b cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:27210752
1332119	Siae	sialic acid acetylesterase	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19103880
1332119	Siae	sialic acid acetylesterase	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:27210752
1332119	Siae	sialic acid acetylesterase	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:19103880
1332120	Cgref1	cell growth regulator with EF hand domain 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1332120	Cgref1	cell growth regulator with EF hand domain 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1332120	Cgref1	cell growth regulator with EF hand domain 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201231	MGI			
1332120	Cgref1	cell growth regulator with EF hand domain 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200402	MGI			
1332120	Cgref1	cell growth regulator with EF hand domain 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1332120	Cgref1	cell growth regulator with EF hand domain 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1332121	Emc3	ER membrane protein complex subunit 3	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20191128	MGI			PMID:31263175
1332121	Emc3	ER membrane protein complex subunit 3	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20210520	MGI			
1332121	Emc3	ER membrane protein complex subunit 3	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:31263175
1332121	Emc3	ER membrane protein complex subunit 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1332121	Emc3	ER membrane protein complex subunit 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1332121	Emc3	ER membrane protein complex subunit 3	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20191128	MGI			PMID:31263175
1332121	Emc3	ER membrane protein complex subunit 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210520	MGI			
1332121	Emc3	ER membrane protein complex subunit 3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1332121	Emc3	ER membrane protein complex subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332122	Emc1	ER membrane protein complex subunit 1	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20240328	MGI			PMID:37098815
1332123	Rasal3	RAS protein activator like 3	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20160707	MGI			PMID:25652366
1332123	Rasal3	RAS protein activator like 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20211021	MGI			
1332123	Rasal3	RAS protein activator like 3	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1332123	Rasal3	RAS protein activator like 3	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
1332123	Rasal3	RAS protein activator like 3	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20160707	MGI			PMID:25652366
1332123	Rasal3	RAS protein activator like 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1332123	Rasal3	RAS protein activator like 3	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1332123	Rasal3	RAS protein activator like 3	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1332123	Rasal3	RAS protein activator like 3	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20160707	MGI			PMID:25652366
1332123	Rasal3	RAS protein activator like 3	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1332123	Rasal3	RAS protein activator like 3	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20181227	MGI			
1332123	Rasal3	RAS protein activator like 3	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20160707	MGI			PMID:25652366
1332123	Rasal3	RAS protein activator like 3	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20160707	MGI			PMID:25652366
1332123	Rasal3	RAS protein activator like 3	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20160707	MGI			PMID:25652366
1332123	Rasal3	RAS protein activator like 3	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20160707	MGI			PMID:25652366
1332123	Rasal3	RAS protein activator like 3	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20160707	MGI			PMID:25652366
1332123	Rasal3	RAS protein activator like 3	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20160707	MGI			PMID:25652366
1332123	Rasal3	RAS protein activator like 3	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18602915
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18602915
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20160421	MGI			PMID:23413146
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0003337	exocrine pancreas hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0003450	enlarged pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20160421	MGI			PMID:23413146
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20201022	MGI			
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740569
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20160421	MGI			PMID:23413146
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20160421	MGI			PMID:23413146
1332124	Serpinf1	serine (or cysteine) peptidase inhibitor, clade F, member 1	gene	MP:0010929	increased osteoid thickness		IAGP		N	RGD:5509061	20160421	MGI			PMID:23413146
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20231207	MGI			
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20231207	MGI			
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0003173	decreased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0004867	decreased platelet calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12445206
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005077	abnormal melanogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005098	abnormal optic choroid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005100	abnormal choroid pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20240523	MGI			
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:12576321
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:11110696
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0030915	abnormal melanosome maturation		IAGP		N	RGD:5509061	20181227	MGI			PMID:12445206
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0030916	abnormal melanosome size		IAGP		N	RGD:5509061	20181227	MGI			PMID:12445206
1332125	Bloc1s4	biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino	gene	MP:0030918	small melanosome		IAGP		N	RGD:5509061	20181227	MGI			PMID:12445206
1332126	Uevld	UEV and lactate/malate dehyrogenase domains	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1332127	Flywch2	FLYWCH family member 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1332127	Flywch2	FLYWCH family member 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1332127	Flywch2	FLYWCH family member 2	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20211021	MGI			
1332128	Eri2	exoribonuclease 2	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20250508	MGI			
1332128	Eri2	exoribonuclease 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1332129	Igsf1	immunoglobulin superfamily, member 1	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:23143598
1332129	Igsf1	immunoglobulin superfamily, member 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20161222	MGI			PMID:23143598
1332129	Igsf1	immunoglobulin superfamily, member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832474
1332129	Igsf1	immunoglobulin superfamily, member 1	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20161222	MGI			PMID:23143598
1332129	Igsf1	immunoglobulin superfamily, member 1	gene	MP:0005119	decreased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20161222	MGI			PMID:23143598
1332129	Igsf1	immunoglobulin superfamily, member 1	gene	MP:0005134	decreased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20161222	MGI			PMID:23143598
1332129	Igsf1	immunoglobulin superfamily, member 1	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20161222	MGI			PMID:23143598
1332131	Mast1	microtubule associated serine/threonine kinase 1	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20190926	MGI			PMID:30449657
1332131	Mast1	microtubule associated serine/threonine kinase 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20190926	MGI			PMID:30449657
1332131	Mast1	microtubule associated serine/threonine kinase 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20190926	MGI			PMID:30449657
1332131	Mast1	microtubule associated serine/threonine kinase 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20190926	MGI			PMID:30449657
1332131	Mast1	microtubule associated serine/threonine kinase 1	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20190926	MGI			PMID:30449657
1332131	Mast1	microtubule associated serine/threonine kinase 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20190926	MGI			PMID:30449657
1332131	Mast1	microtubule associated serine/threonine kinase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190926	MGI			PMID:30449657
1332131	Mast1	microtubule associated serine/threonine kinase 1	gene	MP:0012443	increased corpus callosum size		IAGP		N	RGD:5509061	20190926	MGI			PMID:30449657
1332133	Ntaq1	N-terminal glutamine amidase 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1332133	Ntaq1	N-terminal glutamine amidase 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1332133	Ntaq1	N-terminal glutamine amidase 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1332133	Ntaq1	N-terminal glutamine amidase 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23159736
1332133	Ntaq1	N-terminal glutamine amidase 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230601	MGI			
1332133	Ntaq1	N-terminal glutamine amidase 1	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20230601	MGI			
1332133	Ntaq1	N-terminal glutamine amidase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1332134	Pias3	protein inhibitor of activated STAT 3	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20171214	MGI			PMID:28495965
1332134	Pias3	protein inhibitor of activated STAT 3	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20171214	MGI			PMID:28495965
1332134	Pias3	protein inhibitor of activated STAT 3	gene	MP:0031273	decreased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20240718	MGI			PMID:37008329
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0008926	abnormal anterior definitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15371312
1332135	Dync2li1	dynein cytoplasmic 2 light intermediate chain 1	gene	MP:0030538	abnormal notochordal plate morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15371312
1332138	Cabs1	calcium binding protein, spermatid specific 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210506	MGI			PMID:33440775
1332138	Cabs1	calcium binding protein, spermatid specific 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:33440775
1332138	Cabs1	calcium binding protein, spermatid specific 1	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20201022	MGI			PMID:32588039
1332138	Cabs1	calcium binding protein, spermatid specific 1	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20210506	MGI			PMID:33440775
1332138	Cabs1	calcium binding protein, spermatid specific 1	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33440775
1332138	Cabs1	calcium binding protein, spermatid specific 1	gene	MP:0009835	absent sperm annulus		IAGP		N	RGD:5509061	20210506	MGI			PMID:33440775
1332140	Caml	calcium modulating ligand	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111633
1332140	Caml	calcium modulating ligand	gene	MP:0004918	abnormal negative T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111633
1332140	Caml	calcium modulating ligand	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111633
1332140	Caml	calcium modulating ligand	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111633
1332140	Caml	calcium modulating ligand	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16111633
1332140	Caml	calcium modulating ligand	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12919676
1332141	Rnf34	ring finger protein 34	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0004882	enlarged lung		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1332141	Rnf34	ring finger protein 34	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20250508	MGI			
1332143	Trpv2	transient receptor potential cation channel, subfamily V, member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20118928
1332143	Trpv2	transient receptor potential cation channel, subfamily V, member 2	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20118928
1332143	Trpv2	transient receptor potential cation channel, subfamily V, member 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20118928
1332143	Trpv2	transient receptor potential cation channel, subfamily V, member 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20118928
1332143	Trpv2	transient receptor potential cation channel, subfamily V, member 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20118928
1332145	Commd10	COMM domain containing 10	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:26847029
1332145	Commd10	COMM domain containing 10	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23795291
1332145	Commd10	COMM domain containing 10	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23795291
1332145	Commd10	COMM domain containing 10	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1332145	Commd10	COMM domain containing 10	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20260312	MGI			PMID:34406363
1332145	Commd10	COMM domain containing 10	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20210415	MGI			PMID:29967452
1332145	Commd10	COMM domain containing 10	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:23795291
1332145	Commd10	COMM domain containing 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1332145	Commd10	COMM domain containing 10	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22659386
1332145	Commd10	COMM domain containing 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22186994
1332145	Commd10	COMM domain containing 10	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1332145	Commd10	COMM domain containing 10	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20180201	MGI			PMID:22186994
1332145	Commd10	COMM domain containing 10	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20180201	MGI			PMID:24030045
1332145	Commd10	COMM domain containing 10	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22186994
1332145	Commd10	COMM domain containing 10	gene	MP:0001993	abnormal blinking		IAGP		N	RGD:5509061	20180201	MGI			PMID:28114589
1332145	Commd10	COMM domain containing 10	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1332145	Commd10	COMM domain containing 10	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:21148330
1332145	Commd10	COMM domain containing 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:23795291
1332145	Commd10	COMM domain containing 10	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:23293022
1332145	Commd10	COMM domain containing 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:24894949
1332145	Commd10	COMM domain containing 10	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20180201	MGI			PMID:22659386
1332145	Commd10	COMM domain containing 10	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20180201	MGI			PMID:22659386
1332145	Commd10	COMM domain containing 10	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1332145	Commd10	COMM domain containing 10	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18676810
1332145	Commd10	COMM domain containing 10	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180201	MGI			PMID:24048899
1332145	Commd10	COMM domain containing 10	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1332145	Commd10	COMM domain containing 10	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25129145
1332145	Commd10	COMM domain containing 10	gene	MP:0002491	decreased IgD level		IAGP		N	RGD:5509061	20180201	MGI			PMID:25057009
1332145	Commd10	COMM domain containing 10	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20180201	MGI			PMID:25057009
1332145	Commd10	COMM domain containing 10	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20180201	MGI			PMID:24121508
1332145	Commd10	COMM domain containing 10	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24121508
1332145	Commd10	COMM domain containing 10	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23795291
1332145	Commd10	COMM domain containing 10	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24121508
1332145	Commd10	COMM domain containing 10	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20180201	MGI			PMID:23795291
1332145	Commd10	COMM domain containing 10	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24030045
1332145	Commd10	COMM domain containing 10	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20180201	MGI			PMID:20639863
1332145	Commd10	COMM domain containing 10	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22763442
1332145	Commd10	COMM domain containing 10	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1332145	Commd10	COMM domain containing 10	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23795291
1332145	Commd10	COMM domain containing 10	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24591644
1332145	Commd10	COMM domain containing 10	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1332145	Commd10	COMM domain containing 10	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20180201	MGI			PMID:18676810
1332145	Commd10	COMM domain containing 10	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1332145	Commd10	COMM domain containing 10	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1332145	Commd10	COMM domain containing 10	gene	MP:0004975	absent regulatory T cells		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1332145	Commd10	COMM domain containing 10	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18676810
1332145	Commd10	COMM domain containing 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24591644
1332145	Commd10	COMM domain containing 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1332145	Commd10	COMM domain containing 10	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1332145	Commd10	COMM domain containing 10	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25129145
1332145	Commd10	COMM domain containing 10	gene	MP:0005068	abnormal NK cell morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:29967452
1332145	Commd10	COMM domain containing 10	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20210422	MGI			PMID:26851218
1332145	Commd10	COMM domain containing 10	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18676810
1332145	Commd10	COMM domain containing 10	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1332145	Commd10	COMM domain containing 10	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20180201	MGI			PMID:25129145
1332145	Commd10	COMM domain containing 10	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0005462	abnormal mast cell differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:24204913
1332145	Commd10	COMM domain containing 10	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20180201	MGI			PMID:24121508
1332145	Commd10	COMM domain containing 10	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:27939640
1332145	Commd10	COMM domain containing 10	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22763442
1332145	Commd10	COMM domain containing 10	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20210415	MGI			PMID:29967452
1332145	Commd10	COMM domain containing 10	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20210422	MGI			PMID:26851218
1332145	Commd10	COMM domain containing 10	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20210422	MGI			PMID:26851218
1332145	Commd10	COMM domain containing 10	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1332145	Commd10	COMM domain containing 10	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1332145	Commd10	COMM domain containing 10	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1332145	Commd10	COMM domain containing 10	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24591644
1332145	Commd10	COMM domain containing 10	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20230413	MGI			PMID:35732734
1332145	Commd10	COMM domain containing 10	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18538592
1332145	Commd10	COMM domain containing 10	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371367
1332145	Commd10	COMM domain containing 10	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0008247	abnormal mononuclear cell morphology		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22763442
1332145	Commd10	COMM domain containing 10	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20180201	MGI			PMID:24030045
1332145	Commd10	COMM domain containing 10	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1332145	Commd10	COMM domain containing 10	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20180201	MGI			PMID:24591644
1332145	Commd10	COMM domain containing 10	gene	MP:0008588	abnormal circulating interleukin level		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1332145	Commd10	COMM domain containing 10	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1332145	Commd10	COMM domain containing 10	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20180201	MGI			PMID:24204913
1332145	Commd10	COMM domain containing 10	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20180201	MGI			PMID:25129145
1332145	Commd10	COMM domain containing 10	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20180201	MGI			PMID:25129145
1332145	Commd10	COMM domain containing 10	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20180201	MGI			PMID:18538592
1332145	Commd10	COMM domain containing 10	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371367
1332145	Commd10	COMM domain containing 10	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22659386
1332145	Commd10	COMM domain containing 10	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23795291
1332145	Commd10	COMM domain containing 10	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1332145	Commd10	COMM domain containing 10	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22659386
1332145	Commd10	COMM domain containing 10	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0008998	decreased blood osmolality		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18371367
1332145	Commd10	COMM domain containing 10	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1332145	Commd10	COMM domain containing 10	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21844204
1332145	Commd10	COMM domain containing 10	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0009623	enlarged inguinal lymph nodes		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0009631	enlarged axillary lymph nodes		IAGP		N	RGD:5509061	20230420	MGI			PMID:36062803
1332145	Commd10	COMM domain containing 10	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1332145	Commd10	COMM domain containing 10	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180201	MGI			PMID:24048899
1332145	Commd10	COMM domain containing 10	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:25057009
1332145	Commd10	COMM domain containing 10	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0010130	decreased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0010134	decreased DN3 thymocyte number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21258009
1332145	Commd10	COMM domain containing 10	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1332145	Commd10	COMM domain containing 10	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21339326
1332145	Commd10	COMM domain containing 10	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18656388
1332145	Commd10	COMM domain containing 10	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1332145	Commd10	COMM domain containing 10	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:39947179
1332145	Commd10	COMM domain containing 10	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:23795291
1332145	Commd10	COMM domain containing 10	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190103	MGI			PMID:30423293
1332145	Commd10	COMM domain containing 10	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1332145	Commd10	COMM domain containing 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332145	Commd10	COMM domain containing 10	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:22659386
1332145	Commd10	COMM domain containing 10	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0011177	abnormal erythroblast number		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0011181	increased hematopoietic cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1332145	Commd10	COMM domain containing 10	gene	MP:0011181	increased hematopoietic cell number		IAGP		N	RGD:5509061	20251120	MGI			PMID:38498036
1332145	Commd10	COMM domain containing 10	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22281595
1332145	Commd10	COMM domain containing 10	gene	MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20180201	MGI			PMID:25552701
1332145	Commd10	COMM domain containing 10	gene	MP:0011695	absent hematopoietic stem cells		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0011746	spleen fibrosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0012328	decreased circulating factor VIII level		IAGP		N	RGD:5509061	20180201	MGI			PMID:24705491
1332145	Commd10	COMM domain containing 10	gene	MP:0012384	abnormal erythrocyte ion transport		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20260312	MGI			PMID:34406363
1332145	Commd10	COMM domain containing 10	gene	MP:0012664	decreased circulating haptoglobin level		IAGP		N	RGD:5509061	20180201	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0012765	decreased alpha-beta T cell number		IAGP		N	RGD:5509061	20190530	MGI			PMID:30237863
1332145	Commd10	COMM domain containing 10	gene	MP:0013147	limb paralysis		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0013583	salivary gland degeneration		IAGP		N	RGD:5509061	20220616	MGI			PMID:29127143
1332145	Commd10	COMM domain containing 10	gene	MP:0013659	abnormal erythroid lineage cell morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0013662	decreased myeloid cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0013667	increased immature NK cell number		IAGP		N	RGD:5509061	20210422	MGI			PMID:26851218
1332145	Commd10	COMM domain containing 10	gene	MP:0013672	decreased mature NK cell number		IAGP		N	RGD:5509061	20210422	MGI			PMID:26851218
1332145	Commd10	COMM domain containing 10	gene	MP:0013693	abnormal hemopoiesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0013693	abnormal hemopoiesis		IAGP		N	RGD:5509061	20190516	MGI			PMID:30635284
1332145	Commd10	COMM domain containing 10	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1332145	Commd10	COMM domain containing 10	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0013704	increased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0013705	decreased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1332145	Commd10	COMM domain containing 10	gene	MP:0013707	abnormal hematopoietic precursor cell morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0013891	increased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0013892	increased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22185780
1332145	Commd10	COMM domain containing 10	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:28319097
1332145	Commd10	COMM domain containing 10	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20250605	MGI			PMID:38918373
1332145	Commd10	COMM domain containing 10	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1332145	Commd10	COMM domain containing 10	gene	MP:0014606	dark spleen		IAGP		N	RGD:5509061	20250206	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:18160670
1332145	Commd10	COMM domain containing 10	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:22422825
1332145	Commd10	COMM domain containing 10	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:33753942
1332145	Commd10	COMM domain containing 10	gene	MP:0020463	increased megakaryocyte progenitor cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:29202466
1332145	Commd10	COMM domain containing 10	gene	MP:0020838	increased acute myeloid leukemia incidence		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28114589
1332145	Commd10	COMM domain containing 10	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1332145	Commd10	COMM domain containing 10	gene	MP:0031058	hepatosplenomegaly		IAGP		N	RGD:5509061	20250612	MGI			PMID:38194688
1332145	Commd10	COMM domain containing 10	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:26001274
1332145	Commd10	COMM domain containing 10	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20230330	MGI			PMID:35987460
1332147	Hmbox1	homeobox containing 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220811	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23685356
1332147	Hmbox1	homeobox containing 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220811	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20240523	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20220811	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20220811	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20220811	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1332147	Hmbox1	homeobox containing 1	gene	MP:0009454	impaired contextual conditioning behavior		IEA		N	RGD:5509061	20220811	MGI			
1332150	Nolc1	nucleolar and coiled-body phosphoprotein 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
1332151	Rilpl2	Rab interacting lysosomal protein-like 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1332151	Rilpl2	Rab interacting lysosomal protein-like 2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1332151	Rilpl2	Rab interacting lysosomal protein-like 2	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20260402	MGI			
1332151	Rilpl2	Rab interacting lysosomal protein-like 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:9974390
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21296886
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:21296886
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21296886
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:9974390
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0005472	abnormal triiodothyronine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0005477	increased circulating thyroxine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0005480	increased circulating triiodothyronine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0009301	decreased parametrial fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093799
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21296886
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:12960027
1332152	Gpd2	glycerol phosphate dehydrogenase 2, mitochondrial	gene	MP:0030742	increased aspartic acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17591776
1332153	Mrgprg	MAS-related GPR, member G	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1332153	Mrgprg	MAS-related GPR, member G	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150507	MGI			PMID:24325796
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20150507	MGI			PMID:24325796
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800626
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800627
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15792954
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800626
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800627
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103352
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20250612	MGI			PMID:37696137
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103352
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0008407	decreased cellular sensitivity to hydrogen peroxide		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800626
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19524512
1332155	Ppif	peptidylprolyl isomerase F (cyclophilin F)	gene	MP:0031217	increased susceptibility to myocardial ischemic injury		IAGP		N	RGD:5509061	20250612	MGI			PMID:37696137
1332157	Negr1	neuronal growth regulator 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1332157	Negr1	neuronal growth regulator 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22844493
1332157	Negr1	neuronal growth regulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22844493
1332157	Negr1	neuronal growth regulator 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1332157	Negr1	neuronal growth regulator 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22844493
1332157	Negr1	neuronal growth regulator 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1332157	Negr1	neuronal growth regulator 1	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20210128	MGI			
1332157	Negr1	neuronal growth regulator 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22844493
1332157	Negr1	neuronal growth regulator 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22844493
1332157	Negr1	neuronal growth regulator 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201231	MGI			
1332157	Negr1	neuronal growth regulator 1	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22844493
1332157	Negr1	neuronal growth regulator 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22844493
1332157	Negr1	neuronal growth regulator 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20170105	MGI			
1332157	Negr1	neuronal growth regulator 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1332157	Negr1	neuronal growth regulator 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:22844493
1332157	Negr1	neuronal growth regulator 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1332159	Orm1	orosomucoid 1	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20201022	MGI			PMID:26740279
1332159	Orm1	orosomucoid 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20201022	MGI			PMID:26740279
1332160	Hsd17b11	hydroxysteroid (17-beta) dehydrogenase 11	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1332160	Hsd17b11	hydroxysteroid (17-beta) dehydrogenase 11	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1332160	Hsd17b11	hydroxysteroid (17-beta) dehydrogenase 11	gene	MP:0002960	decreased urine microalbumin level		IEA		N	RGD:5509061	20210520	MGI			
1332160	Hsd17b11	hydroxysteroid (17-beta) dehydrogenase 11	gene	MP:0008214	increased immature B cell number		IEA		N	RGD:5509061	20141003	MGI			
1332160	Hsd17b11	hydroxysteroid (17-beta) dehydrogenase 11	gene	MP:0008500	increased IgG2a level		IEA		N	RGD:5509061	20141003	MGI			
1332160	Hsd17b11	hydroxysteroid (17-beta) dehydrogenase 11	gene	MP:0011471	decreased urine creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1332161	Gldn	gliomedin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20188654
1332161	Gldn	gliomedin	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20188654
1332161	Gldn	gliomedin	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20188654
1332161	Gldn	gliomedin	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20188654
1332162	Chn2	chimerin 2	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726444
1332162	Chn2	chimerin 2	gene	MP:0008960	abnormal axon pruning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726444
1332164	Lin7a	lin-7 homolog A, crumbs cell polarity complex component	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186258
1332164	Lin7a	lin-7 homolog A, crumbs cell polarity complex component	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104771
1332164	Lin7a	lin-7 homolog A, crumbs cell polarity complex component	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186258
1332164	Lin7a	lin-7 homolog A, crumbs cell polarity complex component	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186258
1332164	Lin7a	lin-7 homolog A, crumbs cell polarity complex component	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16186258
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20150611	MGI			PMID:6530139
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20150611	MGI			PMID:6530139
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0002138	abnormal hepatobiliary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20150611	MGI			PMID:6530139
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965258
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0004350	long humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0004357	long tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0004357	long tibia		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0004695	increased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20150611	MGI			PMID:3957811
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20150611	MGI			PMID:3957811
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20230119	MGI			
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0008162	increased diameter of tibia		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0008831	abnormal insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0008951	long radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0009143	abnormal pancreatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0009517	abnormal salivary gland duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10890450
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0010967	increased compact bone area		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20151119	MGI			PMID:18803233
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:22562833
1332166	Socs2	suppressor of cytokine signaling 2	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:22562833
1332167	Hp1bp3	heterochromatin protein 1, binding protein 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160428	MGI			PMID:25662603
1332167	Hp1bp3	heterochromatin protein 1, binding protein 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160428	MGI			PMID:25662603
1332167	Hp1bp3	heterochromatin protein 1, binding protein 3	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20160428	MGI			PMID:25662603
1332167	Hp1bp3	heterochromatin protein 1, binding protein 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160428	MGI			PMID:25662603
1332168	Myom2	myomesin 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1332168	Myom2	myomesin 2	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20200402	MGI			
1332168	Myom2	myomesin 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20250227	MGI			PMID:39255038
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0001432	abnormal food preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:16054071
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16121183
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0001934	increased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215525
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16121183
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0002208	abnormal germ cell morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17343295
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0002451	abnormal macrophage physiology		IEA		N	RGD:5509061	20111116	MGI			
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17343295
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12215525
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20210527	MGI			PMID:31166980
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20210527	MGI			PMID:31166980
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:16121183
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213227
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20250612	MGI			PMID:40106564
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
1332170	Eif2ak4	eukaryotic translation initiation factor 2 alpha kinase 4	gene	MP:0020931	increased susceptibility to Adenoviridae infection		IEA		N	RGD:5509061	20200430	MGI			
1332171	Otos	otospiralin	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632083
1332171	Otos	otospiralin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632083
1332171	Otos	otospiralin	gene	MP:0004294	abnormal type II spiral ligament fibrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632083
1332171	Otos	otospiralin	gene	MP:0004296	abnormal type IV spiral ligament fibrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632083
1332171	Otos	otospiralin	gene	MP:0004414	decreased cochlear microphonics		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632083
1332171	Otos	otospiralin	gene	MP:0004417	decreased cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15632083
1332173	Spice1	spindle and centriole associated protein 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1332173	Spice1	spindle and centriole associated protein 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
1332173	Spice1	spindle and centriole associated protein 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0000756	forelimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10970877
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:10970877
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10970877
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0009180	increased pancreatic delta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0009186	decreased PP cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0009190	increased pancreatic epsilon cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11076772
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10970877
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23382704
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0021103	abnormal ventral interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:10970877
1332174	Nkx6-1	NK6 homeobox 1	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:10970877
1332175	Card19	caspase recruitment domain family, member 19	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20230817	MGI			PMID:36961449
1332175	Card19	caspase recruitment domain family, member 19	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20230817	MGI			PMID:36961449
1332175	Card19	caspase recruitment domain family, member 19	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20230817	MGI			PMID:36961449
1332175	Card19	caspase recruitment domain family, member 19	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20230817	MGI			PMID:36961449
1332175	Card19	caspase recruitment domain family, member 19	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20230817	MGI			PMID:36961449
1332175	Card19	caspase recruitment domain family, member 19	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20230817	MGI			PMID:36961449
1332177	Uts2r	urotensin 2 receptor	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:12770952
1332178	Scfd1	Sec1 family domain containing 1	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241017	MGI			
1332178	Scfd1	Sec1 family domain containing 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1332178	Scfd1	Sec1 family domain containing 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241017	MGI			
1332178	Scfd1	Sec1 family domain containing 1	gene	MP:0004964	absent inner cell mass		IEA		N	RGD:5509061	20241017	MGI			
1332178	Scfd1	Sec1 family domain containing 1	gene	MP:0005028	abnormal trophectoderm morphology		IEA		N	RGD:5509061	20241017	MGI			
1332178	Scfd1	Sec1 family domain containing 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1332178	Scfd1	Sec1 family domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1332178	Scfd1	Sec1 family domain containing 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1332178	Scfd1	Sec1 family domain containing 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1332180	Atg13	autophagy related 13	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20181220	MGI			PMID:26644405
1332180	Atg13	autophagy related 13	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
1332180	Atg13	autophagy related 13	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1332180	Atg13	autophagy related 13	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20181220	MGI			PMID:26644405
1332180	Atg13	autophagy related 13	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20181220	MGI			PMID:26644405
1332180	Atg13	autophagy related 13	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332180	Atg13	autophagy related 13	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20181220	MGI			PMID:26644405
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0008800	increased small intestinal crypt cell apoptosis		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200402	MGI			
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0011705	absent fibroblast proliferation		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0020427	increased hepatocyte karyomegaly		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0021085	increased DNA replication		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332182	Orc1	origin recognition complex, subunit 1	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000519	hydronephrosis		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000644	dextrocardia		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000690	absent spleen		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000694	spleen hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20180301	MGI			PMID:21515572
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20180301	MGI			PMID:21515572
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20180301	MGI			PMID:21515572
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0003178	left pulmonary isomerism		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0004113	abnormal aortic arch morphology		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0004157	interrupted aortic arch		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0006061	right atrial isomerism		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0008461	left atrial isomerism		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0010403	atrial septal defect		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011249	abdominal situs inversus		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011250	abdominal situs ambiguus		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011254	superior-inferior ventricles		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011649	immotile respiratory cilia		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011668	double outlet right ventricle, Taussig bing type		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20141003	MGI			
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0013907	abnormal cerebrospinal fluid flow		IAGP		N	RGD:5509061	20180308	MGI			PMID:29317443
1332183	Ccdc39	coiled-coil domain containing 39	gene	MP:0031515	l-loop transposition of the great arteries		IEA		N	RGD:5509061	20240118	MGI			
1332184	Fbxo38	F-box protein 38	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332184	Fbxo38	F-box protein 38	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:35769260
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10906391
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180719	MGI			PMID:21881209
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:10906391
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:10906391
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0008401	abnormal CD8-positive, alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:10906391
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:10906391
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:10906391
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20180719	MGI			PMID:10906391
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20180719	MGI			PMID:16611851
1332185	Abcb1b	ATP-binding cassette, sub-family B member 1B	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20180719	MGI			PMID:9108099
1332187	Dctn5	dynactin 5	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0000452	abnormal mouth morphology		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0005157	holoprosencephaly		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0009579	acephaly		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0011252	situs inversus totalis		IEA		N	RGD:5509061	20141003	MGI			
1332187	Dctn5	dynactin 5	gene	MP:0011666	double outlet right ventricle, ventricular defect committed to aorta		IEA		N	RGD:5509061	20141003	MGI			
1332188	Klhl41	kelch-like 41	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:28826497
1332188	Klhl41	kelch-like 41	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20180531	MGI			PMID:28826497
1332188	Klhl41	kelch-like 41	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:28826497
1332188	Klhl41	kelch-like 41	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180531	MGI			PMID:28826497
1332188	Klhl41	kelch-like 41	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180531	MGI			PMID:28826497
1332191	Ccdc85a	coiled-coil domain containing 85A	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210826	MGI			
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0012204	abnormal neuronal stem cell physiology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0014619	absent spermatogonia		IAGP		N	RGD:5509061	20250213	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0014631	abnormal elongated spermatid morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0020388	decreased radial glial cell number		IAGP		N	RGD:5509061	20190912	MGI			PMID:29335608
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210422	MGI			PMID:28914256
1332193	Mettl14	methyltransferase 14, N6-adenosine-methyltransferase subunit	gene	MP:0031739	impaired translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:28914256
1332196	Cwc25	CWC25 spliceosome-associated protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1332198	Sgf29	SAGA complex associated factor 29	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20141003	MGI			
1332198	Sgf29	SAGA complex associated factor 29	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1332199	Padi2	peptidyl arginine deiminase, type II	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984079
1332199	Padi2	peptidyl arginine deiminase, type II	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984079
1332199	Padi2	peptidyl arginine deiminase, type II	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1332199	Padi2	peptidyl arginine deiminase, type II	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332200	Tpd52l2	tumor protein D52-like 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1332200	Tpd52l2	tumor protein D52-like 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1332202	Myl12b	myosin, light chain 12B, regulatory	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1332202	Myl12b	myosin, light chain 12B, regulatory	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1332202	Myl12b	myosin, light chain 12B, regulatory	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1332202	Myl12b	myosin, light chain 12B, regulatory	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20160804	MGI			
1332202	Myl12b	myosin, light chain 12B, regulatory	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1332202	Myl12b	myosin, light chain 12B, regulatory	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20160804	MGI			
1332202	Myl12b	myosin, light chain 12B, regulatory	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1332202	Myl12b	myosin, light chain 12B, regulatory	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20160804	MGI			
1332202	Myl12b	myosin, light chain 12B, regulatory	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160804	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20170105	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0003858	enhanced coordination		IEA		N	RGD:5509061	20141003	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160114	MGI			PMID:17906635
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332205	Elovl6	ELOVL fatty acid elongase 6	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:17906635
1332206	Mettl13	methyltransferase 13, eEF1A lysine and N-terminal methyltransferase	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:30178547
1332206	Mettl13	methyltransferase 13, eEF1A lysine and N-terminal methyltransferase	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:30178547
1332206	Mettl13	methyltransferase 13, eEF1A lysine and N-terminal methyltransferase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:30178547
1332206	Mettl13	methyltransferase 13, eEF1A lysine and N-terminal methyltransferase	gene	MP:0031287	bilateral cryptorchism		IAGP		N	RGD:5509061	20220721	MGI			PMID:30178547
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20160421	MGI			
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20190502	MGI			
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20160811	MGI			
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0003875	abnormal hair follicle regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0009535	abnormal skin sebaceous gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0009715	thick epidermis stratum basale		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0010096	abnormal incisor color		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0010126	abnormal distal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0010680	abnormal skin adnexa physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0010699	dilated hair follicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191412
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109354
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9512518
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1332207	Acvr1b	activin A receptor, type 1B	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:21191412
1332209	Pxk	PX domain containing serine/threonine kinase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1332209	Pxk	PX domain containing serine/threonine kinase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1332209	Pxk	PX domain containing serine/threonine kinase	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1332209	Pxk	PX domain containing serine/threonine kinase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1332209	Pxk	PX domain containing serine/threonine kinase	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220519	MGI			
1332209	Pxk	PX domain containing serine/threonine kinase	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1332209	Pxk	PX domain containing serine/threonine kinase	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20220811	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000633	abnormal pituitary gland morphology		IEA		N	RGD:5509061	20111116	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220811	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20111116	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135419
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000866	cerebellum vermis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135419
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:4111750
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320843
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320843
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001134	absent corpus luteum		IEA		N	RGD:5509061	20111116	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20220811	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320843
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11487633
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20150507	MGI			PMID:23732642
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001516	abnormal motor coordination/balance		IEA		N	RGD:5509061	20111116	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001629	abnormal heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230601	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1195260
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:4111750
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001824	abnormal thymus involution		IEA		N	RGD:5509061	20150326	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001867	rhinitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001921	reduced fertility		IEA		N	RGD:5509061	20111116	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001922	reduced male fertility		IEA		N	RGD:5509061	20111116	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1195260
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220811	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:4111750
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20141003	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20160218	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:4111750
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20220811	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20150507	MGI			PMID:23732642
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135419
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20220811	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11487633
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20150507	MGI			PMID:23732642
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11487633
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320843
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0004706	short vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17320843
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11487633
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0005202	lethargy		IEA		N	RGD:5509061	20111116	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331424
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135419
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:5456441
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9349522
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0008035	behavioral arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0008333	absent lactotrophs		IAGP		N	RGD:5509061	20141003	MGI			PMID:1195260
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0008770	decreased survivor rate		IEA		N	RGD:5509061	20111116	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:11487633
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:4111750
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20150507	MGI			PMID:23732642
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0009460	skeletal muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:4177347
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14660671
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:17135419
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0014947	abnormal liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:5456441
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0014973	abnormal kidney enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:5456441
1332210	Cacna2d2	calcium channel, voltage-dependent, alpha 2/delta subunit 2	gene	MP:0020533	decreased pons size		IAGP		N	RGD:5509061	20180301	MGI			PMID:4177347
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000275	heart hyperplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8806812
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:21212806
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:7671324
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:2554496
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:19299624
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002763	ectopic Bergmann glia cells		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0004545	enlarged esophagus		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0006097	abnormal cerebellar lobule formation		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0006098	absent cerebellar lobules		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0006321	increased myocardial fiber number		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19299624
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7671324
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7671324
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7671324
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20180719	MGI			PMID:21212806
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009216	abnormal peritoneum morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009268	absent cerebellum fissure		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19299624
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:7671324
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8806812
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15987940
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0009978	abnormal cerebellum white matter morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065352
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:2065353
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:8700526
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0013551	decreased cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:20980600
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:20080568
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:19299624
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20190704	MGI			PMID:9883720
1332211	Abl1	Abl proto-oncogene 1, non-receptor tyrosine kinase	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:20080568
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18658108
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802071
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20170105	MGI			
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20170105	MGI			
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983582
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802071
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802071
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802071
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18658108
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983582
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983582
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18658108
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17983582
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18658108
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332214	Nampt	nicotinamide phosphoribosyltransferase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1332215	Lacc1	laccase domain containing 1	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332215	Lacc1	laccase domain containing 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20180315	MGI			PMID:27478939
1332216	Samm50	SAMM50 sorting and assembly machinery component	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20230119	MGI			
1332216	Samm50	SAMM50 sorting and assembly machinery component	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230119	MGI			
1332216	Samm50	SAMM50 sorting and assembly machinery component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1332217	Lin54	lin-54 DREAM MuvB core complex component	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20260402	MGI			
1332217	Lin54	lin-54 DREAM MuvB core complex component	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1332217	Lin54	lin-54 DREAM MuvB core complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20251204	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:19188447
1332218	Use1	unconventional SNARE in the ER 1 homolog (S. cerevisiae)	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20161013	MGI			PMID:19188447
1332219	Ca3	carbonic anhydrase 3	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509796
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185832
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270129
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646578
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646578
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185832
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001598	abnormal blood viscosity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646578
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002450	abnormal lymph organ development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:22955912
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270129
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0003223	decreased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270129
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646578
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646578
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004120	cardiac ischemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20185832
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646578
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646578
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005575	increased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005585	increased tidal volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17646578
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22955912
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20240118	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0010127	hypervolemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270129
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217150
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21270129
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18096761
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011286	decreased circulating erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22955912
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011287	increased erythropoietin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733101
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20240118	MGI			PMID:16966370
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0012397	abnormal nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23264599
1332220	Egln1	egl-9 family hypoxia-inducible factor 1	gene	MP:0020327	abnormal capillary branching pattern		IAGP		N	RGD:5509061	20160714	MGI			PMID:17646578
1332221	Krt13	keratin 13	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:32758484
1332221	Krt13	keratin 13	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:32758484
1332221	Krt13	keratin 13	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:32758484
1332221	Krt13	keratin 13	gene	MP:0030179	abnormal oral epithelium morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:32758484
1332223	Tmem178	transmembrane protein 178	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332223	Tmem178	transmembrane protein 178	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332223	Tmem178	transmembrane protein 178	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332223	Tmem178	transmembrane protein 178	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332223	Tmem178	transmembrane protein 178	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332223	Tmem178	transmembrane protein 178	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332223	Tmem178	transmembrane protein 178	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332223	Tmem178	transmembrane protein 178	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332223	Tmem178	transmembrane protein 178	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332223	Tmem178	transmembrane protein 178	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20161103	MGI			PMID:26644563
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220922	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000130	abnormal trabecular bone morphology		IEA		N	RGD:5509061	20111116	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0000755	hindlimb paralysis		IEA		N	RGD:5509061	20111116	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20111116	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20111116	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20410296
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20111116	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0003116	rickets		IEA		N	RGD:5509061	20111116	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0005245	hemarthrosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20231207	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0009864	abnormal aorta endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0011229	abnormal vitamin C level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639167
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0011229	abnormal vitamin C level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20410296
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:11062347
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0030827	femur fracture		IEA		N	RGD:5509061	20181018	MGI			
1332224	Gulo	gulonolactone (L-) oxidase	gene	MP:0030884	rachitic rosary		IAGP		N	RGD:5509061	20181101	MGI			PMID:20410296
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0009974	decreased cerebral cortex pyramidal cell number		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200310	MGI			
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200310	MGI			
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332226	Atp6v0a1	ATPase, H+ transporting, lysosomal V0 subunit A1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20210603	MGI			PMID:33833240
1332227	Pdcd2l	programmed cell death 2-like	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210715	MGI			PMID:33055224
1332227	Pdcd2l	programmed cell death 2-like	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20210715	MGI			PMID:33055224
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1332228	2310061I04Rik	RIKEN cDNA 2310061I04 gene	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0010732	abnormal node of Ranvier morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0014331	abnormal Purkinje cell mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:28376086
1332229	Slc25a46	solute carrier family 25, member 46	gene	MP:0020339	abnormal retina ganglion cell dendrite morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:28376086
1332231	Ppil3	peptidylprolyl isomerase (cyclophilin)-like 3	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20160421	MGI			
1332231	Ppil3	peptidylprolyl isomerase (cyclophilin)-like 3	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1332231	Ppil3	peptidylprolyl isomerase (cyclophilin)-like 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201231	MGI			
1332231	Ppil3	peptidylprolyl isomerase (cyclophilin)-like 3	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1332231	Ppil3	peptidylprolyl isomerase (cyclophilin)-like 3	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20170105	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20150430	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20240627	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20150430	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20160114	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20240627	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332232	Zhx3	zinc fingers and homeoboxes 3	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1332234	Atxn3	ataxin 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20160317	MGI			PMID:25301414
1332234	Atxn3	ataxin 3	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:25301414
1332234	Atxn3	ataxin 3	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160317	MGI			PMID:25301414
1332234	Atxn3	ataxin 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17764659
1332234	Atxn3	ataxin 3	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20160317	MGI			PMID:25301414
1332234	Atxn3	ataxin 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17764659
1332234	Atxn3	ataxin 3	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:25301414
1332234	Atxn3	ataxin 3	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20151015	MGI			PMID:25320121
1332234	Atxn3	ataxin 3	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20160317	MGI			PMID:25301414
1332234	Atxn3	ataxin 3	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20251023	MGI			PMID:34716557
1332234	Atxn3	ataxin 3	gene	MP:0004794	increased anti-nuclear antigen antibody level		IEA		N	RGD:5509061	20201022	MGI			
1332234	Atxn3	ataxin 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1332234	Atxn3	ataxin 3	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20201022	MGI			
1332234	Atxn3	ataxin 3	gene	MP:0011975	neuronal cytoplasmic inclusions		IAGP		N	RGD:5509061	20151015	MGI			PMID:25320121
1332234	Atxn3	ataxin 3	gene	MP:0011975	neuronal cytoplasmic inclusions		IAGP		N	RGD:5509061	20160317	MGI			PMID:25301414
1332234	Atxn3	ataxin 3	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:25301414
1332235	Sla	src-like adaptor	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567635
1332235	Sla	src-like adaptor	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220694
1332235	Sla	src-like adaptor	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567635
1332235	Sla	src-like adaptor	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567635
1332235	Sla	src-like adaptor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567635
1332235	Sla	src-like adaptor	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220694
1332235	Sla	src-like adaptor	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220694
1332235	Sla	src-like adaptor	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220694
1332239	Arhgap44	Rho GTPase activating protein 44	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1332239	Arhgap44	Rho GTPase activating protein 44	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180111	MGI			PMID:26969129
1332239	Arhgap44	Rho GTPase activating protein 44	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20180111	MGI			PMID:26969129
1332239	Arhgap44	Rho GTPase activating protein 44	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20180111	MGI			PMID:26969129
1332239	Arhgap44	Rho GTPase activating protein 44	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20180111	MGI			PMID:26969129
1332239	Arhgap44	Rho GTPase activating protein 44	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20180111	MGI			PMID:26969129
1332239	Arhgap44	Rho GTPase activating protein 44	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:26969129
1332239	Arhgap44	Rho GTPase activating protein 44	gene	MP:0020512	abnormal dendritic mushroom spine morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:26969129
1332239	Arhgap44	Rho GTPase activating protein 44	gene	MP:0020513	abnormal dendritic stubby spine morphology		IAGP		N	RGD:5509061	20180111	MGI			PMID:26969129
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20190523	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20190523	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20190523	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20190523	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190523	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20190523	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20190523	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20190523	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0014040	increased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20190523	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:25066119
1332240	Abraxas1	BRCA1 A complex subunit	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:25066119
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20191003	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191003	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20191003	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191003	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20191003	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20191003	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0012081	absent heart tube		IAGP		N	RGD:5509061	20191003	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0014395	increased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20250911	MGI			PMID:31036713
1332241	Tefm	transcription elongation factor, mitochondrial	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:31036713
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0002807	abnormal eye blink conditioning behavior		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20181227	MGI			
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332242	Sipa1l1	signal-induced proliferation-associated 1 like 1	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20240509	MGI			PMID:35121636
1332244	Tmub2	transmembrane and ubiquitin-like domain containing 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1332244	Tmub2	transmembrane and ubiquitin-like domain containing 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1332244	Tmub2	transmembrane and ubiquitin-like domain containing 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1332244	Tmub2	transmembrane and ubiquitin-like domain containing 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230601	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20230601	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14659506
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060708
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553498
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0002738	hyperresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060708
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060708
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230601	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20230601	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17531389
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0005407	hyperalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11754838
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:14659506
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008103	amacrine cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008512	disorganized retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008532	decreased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060708
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117938
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553498
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20230601	MGI			
1332245	Asic3	acid-sensing ion channel 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051137
1332250	Epn1	epsin 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23187125
1332250	Epn1	epsin 1	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23187125
1332250	Epn1	epsin 1	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20160623	MGI			PMID:23187125
1332250	Epn1	epsin 1	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23187125
1332250	Epn1	epsin 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23187125
1332250	Epn1	epsin 1	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0005222	abnormal somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23187125
1332250	Epn1	epsin 1	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23187125
1332250	Epn1	epsin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19666558
1332250	Epn1	epsin 1	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23187125
1332250	Epn1	epsin 1	gene	MP:0020161	increased vascular endothelial cell proliferation		IAGP		N	RGD:5509061	20160623	MGI			PMID:23187125
1332251	Scn3b	sodium channel, voltage-gated, type III, beta	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20150108	MGI			
1332251	Scn3b	sodium channel, voltage-gated, type III, beta	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19351516
1332251	Scn3b	sodium channel, voltage-gated, type III, beta	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1332251	Scn3b	sodium channel, voltage-gated, type III, beta	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20201231	MGI			
1332251	Scn3b	sodium channel, voltage-gated, type III, beta	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20260528	MGI			PMID:19351516
1332251	Scn3b	sodium channel, voltage-gated, type III, beta	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19351516
1332251	Scn3b	sodium channel, voltage-gated, type III, beta	gene	MP:0011157	abnormal hypodermis muscle layer morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:25340873
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572694
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956719
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0003437	abnormal carotid body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0003438	abnormal carotid body physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572694
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20180111	MGI			PMID:28204537
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:5509061	20180111	MGI			PMID:28204537
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0008504	abnormal adrenal chromaffin cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711987
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572694
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19956719
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572694
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0020840	abnormal type I cell of carotid body morphology		IAGP		N	RGD:5509061	20181101	MGI			PMID:15572694
1332252	Sdhd	succinate dehydrogenase complex, subunit D, integral membrane protein	gene	MP:0020843	abnormal type I cell of carotid body physiology		IAGP		N	RGD:5509061	20181101	MGI			PMID:15572694
1332253	Pomgnt2	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:24256719
1332253	Pomgnt2	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20151001	MGI			PMID:24256719
1332253	Pomgnt2	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	gene	MP:0004273	abnormal basal lamina morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:24256719
1332253	Pomgnt2	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20151001	MGI			PMID:24256719
1332253	Pomgnt2	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20151001	MGI			PMID:24256719
1332253	Pomgnt2	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20151001	MGI			PMID:24256719
1332253	Pomgnt2	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20151001	MGI			PMID:24256719
1332253	Pomgnt2	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151001	MGI			PMID:24256719
1332253	Pomgnt2	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	gene	MP:0020391	radial glial endfoot detachment		IAGP		N	RGD:5509061	20161117	MGI			PMID:24256719
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550287
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087873
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087873
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087873
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550287
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002676	uterus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550287
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0002936	joint swelling		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550287
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087873
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550287
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0003711	pathological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16087873
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0005488	bronchial epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550287
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550287
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439667
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20418913
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648858
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0010887	pale lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0010910	bronchiolar epithelial hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0010942	abnormal respiratory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0010945	lung epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17987665
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19710174
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0011692	increased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24550287
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20141218	MGI			PMID:19439667
1332254	Errfi1	ERBB receptor feedback inhibitor 1	gene	MP:0030332	accelerated temporomandibular joint osteoarthritis		IAGP		N	RGD:5509061	20171109	MGI			PMID:16087873
1332256	Zfp622	zinc finger protein 622	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20240926	MGI			
1332256	Zfp622	zinc finger protein 622	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1332256	Zfp622	zinc finger protein 622	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1332256	Zfp622	zinc finger protein 622	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20240926	MGI			
1332256	Zfp622	zinc finger protein 622	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20240926	MGI			
1332256	Zfp622	zinc finger protein 622	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230601	MGI			
1332257	Emc4	ER membrane protein complex subunit 4	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170105	MGI			
1332257	Emc4	ER membrane protein complex subunit 4	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1332257	Emc4	ER membrane protein complex subunit 4	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1332257	Emc4	ER membrane protein complex subunit 4	gene	MP:0010580	decreased heart left ventricle size		IEA		N	RGD:5509061	20211021	MGI			
1332257	Emc4	ER membrane protein complex subunit 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332257	Emc4	ER membrane protein complex subunit 4	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1332258	Wrnip1	Werner helicase interacting protein 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1332258	Wrnip1	Werner helicase interacting protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20201022	MGI			
1332258	Wrnip1	Werner helicase interacting protein 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20190502	MGI			
1332258	Wrnip1	Werner helicase interacting protein 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1332258	Wrnip1	Werner helicase interacting protein 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1332258	Wrnip1	Werner helicase interacting protein 1	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20160804	MGI			
1332258	Wrnip1	Werner helicase interacting protein 1	gene	MP:0005316	abnormal response to tactile stimuli		IEA		N	RGD:5509061	20160804	MGI			
1332258	Wrnip1	Werner helicase interacting protein 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20190502	MGI			
1332258	Wrnip1	Werner helicase interacting protein 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20200402	MGI			
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0004420	parietal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0004459	small alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0004476	absent palatine bone		IAGP		N	RGD:5509061	20171116	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20201022	MGI			
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0030353	wide sagittal suture		IAGP		N	RGD:5509061	20171116	MGI			PMID:19706529
1332260	Bnc2	basonuclin zinc finger protein 2	gene	MP:0030387	large posterior fontanelle		IAGP		N	RGD:5509061	20171207	MGI			PMID:19706529
1332263	Gcgr	glucagon receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:28591637
1332263	Gcgr	glucagon receptor	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32677665
1332263	Gcgr	glucagon receptor	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20200310	MGI			PMID:25157166
1332263	Gcgr	glucagon receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25157166
1332263	Gcgr	glucagon receptor	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200310	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:10621976
1332263	Gcgr	glucagon receptor	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0002710	increased glucagon secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11785978
1332263	Gcgr	glucagon receptor	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28591637
1332263	Gcgr	glucagon receptor	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20210429	MGI			PMID:32677665
1332263	Gcgr	glucagon receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28591637
1332263	Gcgr	glucagon receptor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20210429	MGI			PMID:32677665
1332263	Gcgr	glucagon receptor	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20200310	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0003365	increased glucagonoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0003450	enlarged pancreas		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20231207	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20210128	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28591637
1332263	Gcgr	glucagon receptor	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32677665
1332263	Gcgr	glucagon receptor	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:25157166
1332263	Gcgr	glucagon receptor	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20210429	MGI			PMID:32677665
1332263	Gcgr	glucagon receptor	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28591637
1332263	Gcgr	glucagon receptor	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:28591637
1332263	Gcgr	glucagon receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20231207	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25157166
1332263	Gcgr	glucagon receptor	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:25157166
1332263	Gcgr	glucagon receptor	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20210429	MGI			PMID:32677665
1332263	Gcgr	glucagon receptor	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28591637
1332263	Gcgr	glucagon receptor	gene	MP:0009179	abnormal pancreatic alpha cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25157166
1332263	Gcgr	glucagon receptor	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1332263	Gcgr	glucagon receptor	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12552113
1332263	Gcgr	glucagon receptor	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:25157166
1332263	Gcgr	glucagon receptor	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31230984
1332263	Gcgr	glucagon receptor	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20210429	MGI			PMID:32677665
1332263	Gcgr	glucagon receptor	gene	MP:0013558	abnormal exocrine gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853126
1332263	Gcgr	glucagon receptor	gene	MP:0014109	increased pancreatic alpha cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0014109	increased pancreatic alpha cell proliferation		IAGP		N	RGD:5509061	20210429	MGI			PMID:32677665
1332263	Gcgr	glucagon receptor	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20210429	MGI			PMID:32677665
1332263	Gcgr	glucagon receptor	gene	MP:0020090	decreased susceptibility to diet-induced non-insulin dependent diabetes		IAGP		N	RGD:5509061	20200310	MGI			PMID:25157166
1332263	Gcgr	glucagon receptor	gene	MP:0030589	increased pancreatic alpha cell mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23160527
1332263	Gcgr	glucagon receptor	gene	MP:0031270	decreased susceptibility to age-related hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:21853126
1332267	Ift43	intraflagellar transport 43	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20181227	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20181227	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20181227	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20181227	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20181227	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20181227	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20181227	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332267	Ift43	intraflagellar transport 43	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1332268	Pfdn6	prefoldin subunit 6	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20170105	MGI			
1332268	Pfdn6	prefoldin subunit 6	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1332268	Pfdn6	prefoldin subunit 6	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210826	MGI			
1332268	Pfdn6	prefoldin subunit 6	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1332268	Pfdn6	prefoldin subunit 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332270	Tbck	TBC1 domain containing kinase	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20240229	MGI			PMID:37353954
1332270	Tbck	TBC1 domain containing kinase	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20240229	MGI			PMID:37353954
1332270	Tbck	TBC1 domain containing kinase	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20240229	MGI			PMID:37353954
1332270	Tbck	TBC1 domain containing kinase	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20240229	MGI			PMID:37353954
1332270	Tbck	TBC1 domain containing kinase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0002959	increased urine microalbumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0009552	urinary bladder obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0009646	urinary bladder inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332271	Gstk1	glutathione S-transferase kappa 1	gene	MP:0011763	urethritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21826057
1332274	Kmt5a	lysine methyltransferase 5A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223465
1332274	Kmt5a	lysine methyltransferase 5A	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223465
1332274	Kmt5a	lysine methyltransferase 5A	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223465
1332274	Kmt5a	lysine methyltransferase 5A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223465
1332274	Kmt5a	lysine methyltransferase 5A	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223465
1332274	Kmt5a	lysine methyltransferase 5A	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223465
1332274	Kmt5a	lysine methyltransferase 5A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18319261
1332274	Kmt5a	lysine methyltransferase 5A	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223465
1332274	Kmt5a	lysine methyltransferase 5A	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:19223465
1332275	Mphosph8	M-phase phosphoprotein 8	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1332275	Mphosph8	M-phase phosphoprotein 8	gene	MP:0000899	abnormal corpora quadrigemina morphology		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1332275	Mphosph8	M-phase phosphoprotein 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1332275	Mphosph8	M-phase phosphoprotein 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1332275	Mphosph8	M-phase phosphoprotein 8	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20221103	MGI			
1332275	Mphosph8	M-phase phosphoprotein 8	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1332275	Mphosph8	M-phase phosphoprotein 8	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1332275	Mphosph8	M-phase phosphoprotein 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20221103	MGI			
1332275	Mphosph8	M-phase phosphoprotein 8	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230601	MGI			
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19164486
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20200310	MGI			
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0009854	impaired gastric peristalsis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24993824
1332276	P2ry14	purinergic receptor P2Y, G-protein coupled, 14	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242209
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242209
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242209
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242209
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242209
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242209
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242209
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242209
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0008902	abnormal renal fat pad morphology		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242209
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332277	Trp53inp1	transformation related protein 53 inducible nuclear protein 1	gene	MP:0020089	increased susceptibility to diet-induced non-insulin dependent diabetes		IAGP		N	RGD:5509061	20170427	MGI			PMID:25828351
1332278	Enoph1	enolase-phosphatase 1	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20231109	MGI			PMID:37075968
1332278	Enoph1	enolase-phosphatase 1	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20231109	MGI			PMID:37075968
1332280	Aftph	aftiphilin	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20230601	MGI			
1332280	Aftph	aftiphilin	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1332280	Aftph	aftiphilin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20181227	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20181227	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20210826	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332281	Ints10	integrator complex subunit 10	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1332282	Ttc12	tetratricopeptide repeat domain 12	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20250508	MGI			
1332282	Ttc12	tetratricopeptide repeat domain 12	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1332282	Ttc12	tetratricopeptide repeat domain 12	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20260402	MGI			
1332282	Ttc12	tetratricopeptide repeat domain 12	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1332282	Ttc12	tetratricopeptide repeat domain 12	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20260402	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210520	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20181227	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210520	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20190502	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210520	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20181227	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20201022	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20210520	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20210520	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20181227	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0005313	absent adrenal gland		IEA		N	RGD:5509061	20210520	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20240523	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20181227	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1332284	Adnp2	ADNP homeobox 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1332286	Tmem218	transmembrane protein 218	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20160114	MGI			PMID:25161209
1332286	Tmem218	transmembrane protein 218	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:25161209
1332288	Cip2a	cell proliferation regulating inhibitor of protein phosphatase 2A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461891
1332288	Cip2a	cell proliferation regulating inhibitor of protein phosphatase 2A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461891
1332288	Cip2a	cell proliferation regulating inhibitor of protein phosphatase 2A	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461891
1332288	Cip2a	cell proliferation regulating inhibitor of protein phosphatase 2A	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461891
1332289	Apln	apelin	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200044
1332289	Apln	apelin	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200044
1332289	Apln	apelin	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200044
1332289	Apln	apelin	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767528
1332289	Apln	apelin	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17673668
1332289	Apln	apelin	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767528
1332289	Apln	apelin	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767528
1332289	Apln	apelin	gene	MP:0005412	vascular stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18200044
1332289	Apln	apelin	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767528
1332289	Apln	apelin	gene	MP:0020329	decreased capillary density		IAGP		N	RGD:5509061	20160714	MGI			PMID:18200044
1332289	Apln	apelin	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:17673668
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000155	asymmetric rib joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000346	broad head		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639082
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20220519	MGI			
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004445	small exoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004472	broad nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20230601	MGI			
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17639082
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0008901	absent epididymal fat pad		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20171207	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0030069	broad face		IAGP		N	RGD:5509061	20171207	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0030288	broad occipital bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:16980622
1332291	Psip1	PC4 and SFRS1 interacting protein 1	gene	MP:0030289	flat occipital bone		IAGP		N	RGD:5509061	20171102	MGI			PMID:16980622
1332292	Prag1	PEAK1 related kinase activating pseudokinase 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1332292	Prag1	PEAK1 related kinase activating pseudokinase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160616	MGI			PMID:25038227
1332292	Prag1	PEAK1 related kinase activating pseudokinase 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1332293	Aco2	aconitase 2, mitochondrial	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1332295	Exoc6	exocyst complex component 6	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:16289749
1332295	Exoc6	exocyst complex component 6	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:9292544
1332295	Exoc6	exocyst complex component 6	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9292544
1332295	Exoc6	exocyst complex component 6	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:4596202
1332295	Exoc6	exocyst complex component 6	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1332295	Exoc6	exocyst complex component 6	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:4596202
1332295	Exoc6	exocyst complex component 6	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16289749
1332295	Exoc6	exocyst complex component 6	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:4596202
1332295	Exoc6	exocyst complex component 6	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:16289749
1332295	Exoc6	exocyst complex component 6	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:9292544
1332295	Exoc6	exocyst complex component 6	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16289749
1332295	Exoc6	exocyst complex component 6	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:9292544
1332295	Exoc6	exocyst complex component 6	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9292544
1332295	Exoc6	exocyst complex component 6	gene	MP:0002814	hyperchromasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:4596202
1332295	Exoc6	exocyst complex component 6	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:16289749
1332295	Exoc6	exocyst complex component 6	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:9292544
1332295	Exoc6	exocyst complex component 6	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:4596202
1332295	Exoc6	exocyst complex component 6	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1332295	Exoc6	exocyst complex component 6	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20200310	MGI			
1332295	Exoc6	exocyst complex component 6	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:4596202
1332295	Exoc6	exocyst complex component 6	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1332295	Exoc6	exocyst complex component 6	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20200310	MGI			PMID:4596202
1332295	Exoc6	exocyst complex component 6	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16289749
1332295	Exoc6	exocyst complex component 6	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20200310	MGI			PMID:9292544
1332295	Exoc6	exocyst complex component 6	gene	MP:0008387	hypochromic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:4596202
1332295	Exoc6	exocyst complex component 6	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0009931	abnormal skin appearance		IEA		N	RGD:5509061	20200310	MGI			
1332295	Exoc6	exocyst complex component 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:4596202
1332295	Exoc6	exocyst complex component 6	gene	MP:0011188	increased erythrocyte protoporphyrin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0011188	increased erythrocyte protoporphyrin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:9292544
1332295	Exoc6	exocyst complex component 6	gene	MP:0031084	decreased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:3960859
1332295	Exoc6	exocyst complex component 6	gene	MP:0031084	decreased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:4596202
1332296	Mtdh	metadherin	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24981741
1332296	Mtdh	metadherin	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20200310	MGI			PMID:24981741
1332296	Mtdh	metadherin	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:24981741
1332296	Mtdh	metadherin	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332296	Mtdh	metadherin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332296	Mtdh	metadherin	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:24981741
1332296	Mtdh	metadherin	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332296	Mtdh	metadherin	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332296	Mtdh	metadherin	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332296	Mtdh	metadherin	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:24981741
1332296	Mtdh	metadherin	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20200310	MGI			PMID:24981741
1332296	Mtdh	metadherin	gene	MP:0010266	decreased liver tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332296	Mtdh	metadherin	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332296	Mtdh	metadherin	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24981741
1332296	Mtdh	metadherin	gene	MP:0010282	decreased organ/body region tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332296	Mtdh	metadherin	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24981741
1332296	Mtdh	metadherin	gene	MP:0011986	decreased macrophage proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332296	Mtdh	metadherin	gene	MP:0012419	decreased cardiovascular system tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25193383
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332298	Pik3c2g	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20160714	MGI			PMID:26100075
1332300	Duox2	dual oxidase 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20220915	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20201022	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20201022	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210826	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20201022	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1332300	Duox2	dual oxidase 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20201022	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20201022	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1332300	Duox2	dual oxidase 2	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20200514	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20200514	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210128	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1332300	Duox2	dual oxidase 2	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0003498	thyroid gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0004664	delayed inner ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0004692	small pubis		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1332300	Duox2	dual oxidase 2	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200514	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0011721	abnormal bone mineralization involved in bone maturation		IAGP		N	RGD:5509061	20150319	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1332300	Duox2	dual oxidase 2	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20150319	MGI			PMID:17440044
1332300	Duox2	dual oxidase 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1332302	Mitd1	MIT, microtubule interacting and transport, domain containing 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20260402	MGI			
1332302	Mitd1	MIT, microtubule interacting and transport, domain containing 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1332305	Insig1	insulin induced gene 1	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20210128	MGI			
1332305	Insig1	insulin induced gene 1	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1332305	Insig1	insulin induced gene 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:23919961
1332305	Insig1	insulin induced gene 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23919961
1332305	Insig1	insulin induced gene 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1332305	Insig1	insulin induced gene 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210520	MGI			
1332305	Insig1	insulin induced gene 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0002139	abnormal hepatobiliary system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23919961
1332305	Insig1	insulin induced gene 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1332305	Insig1	insulin induced gene 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
1332305	Insig1	insulin induced gene 1	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20221215	MGI			
1332305	Insig1	insulin induced gene 1	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23919961
1332305	Insig1	insulin induced gene 1	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23919961
1332305	Insig1	insulin induced gene 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16100574
1332305	Insig1	insulin induced gene 1	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23919961
1332305	Insig1	insulin induced gene 1	gene	MP:0011169	abnormal white fat cell differentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23919961
1332305	Insig1	insulin induced gene 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1332305	Insig1	insulin induced gene 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18838740
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18838740
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18838740
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20240523	MGI			
1332308	Elovl5	ELOVL fatty acid elongase 5	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1332311	Gins4	GINS complex subunit 4	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20190502	MGI			
1332311	Gins4	GINS complex subunit 4	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1332311	Gins4	GINS complex subunit 4	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1332311	Gins4	GINS complex subunit 4	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244394
1332311	Gins4	GINS complex subunit 4	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20211021	MGI			
1332311	Gins4	GINS complex subunit 4	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244394
1332311	Gins4	GINS complex subunit 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332311	Gins4	GINS complex subunit 4	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20211021	MGI			
1332311	Gins4	GINS complex subunit 4	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244394
1332311	Gins4	GINS complex subunit 4	gene	MP:0012743	increased inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24244394
1332311	Gins4	GINS complex subunit 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0000296	absent trabeculae carneae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210826	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1332312	Xbp1	X-box binding protein 1	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24089213
1332312	Xbp1	X-box binding protein 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18556558
1332312	Xbp1	X-box binding protein 1	gene	MP:0002316	anoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20170105	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18556558
1332312	Xbp1	X-box binding protein 1	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24089213
1332312	Xbp1	X-box binding protein 1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20190523	MGI			PMID:30254094
1332312	Xbp1	X-box binding protein 1	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160804	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20191128	MGI			PMID:29551634
1332312	Xbp1	X-box binding protein 1	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18556558
1332312	Xbp1	X-box binding protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0004264	abnormal extraembryonic tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1332312	Xbp1	X-box binding protein 1	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20141003	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24089213
1332312	Xbp1	X-box binding protein 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20160804	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18556558
1332312	Xbp1	X-box binding protein 1	gene	MP:0005363	decreased susceptibility to prion infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178615
1332312	Xbp1	X-box binding protein 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0008142	decreased small intestinal villus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24089213
1332312	Xbp1	X-box binding protein 1	gene	MP:0008495	decreased IgG1 level		IEA		N	RGD:5509061	20160804	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24089213
1332312	Xbp1	X-box binding protein 1	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20190523	MGI			PMID:30254094
1332312	Xbp1	X-box binding protein 1	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24089213
1332312	Xbp1	X-box binding protein 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160804	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10652269
1332312	Xbp1	X-box binding protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23529610
1332312	Xbp1	X-box binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0012361	decreased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1332312	Xbp1	X-box binding protein 1	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10425189
1332312	Xbp1	X-box binding protein 1	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0013792	abnormal small intestine goblet cell morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0014076	absent Paneth cells		IAGP		N	RGD:5509061	20160310	MGI			PMID:18775308
1332312	Xbp1	X-box binding protein 1	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20191128	MGI			PMID:29551634
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0014384	increased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0020358	abnormal inhibitory synapse morphology		IAGP		N	RGD:5509061	20211118	MGI			PMID:27875292
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0020870	decreased thigmotaxis		IAGP		N	RGD:5509061	20200917	MGI			PMID:31183559
1332314	Zdhhc7	zinc finger, DHHC domain containing 7	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:31183559
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1332315	Hibadh	3-hydroxyisobutyrate dehydrogenase	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210520	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20220519	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20210520	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210520	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20210826	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20210520	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210520	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210826	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20210520	MGI			
1332316	Fgfr1op2	FGFR1 oncogene partner 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0004230	abnormal embryonic erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20201231	MGI			
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0009131	decreased white fat cell number		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0011169	abnormal white fat cell differentation		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0011702	abnormal fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467409
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332317	Arhgef11	Rho guanine nucleotide exchange factor 11	gene	MP:0020090	decreased susceptibility to diet-induced non-insulin dependent diabetes		IAGP		N	RGD:5509061	20161013	MGI			PMID:26512886
1332318	Cpxm2	carboxypeptidase X, M14 family member 2	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:34916661
1332318	Cpxm2	carboxypeptidase X, M14 family member 2	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20240307	MGI			PMID:34916661
1332318	Cpxm2	carboxypeptidase X, M14 family member 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20240307	MGI			PMID:34916661
1332318	Cpxm2	carboxypeptidase X, M14 family member 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20240307	MGI			PMID:34916661
1332318	Cpxm2	carboxypeptidase X, M14 family member 2	gene	MP:0020204	abnormal heart left ventricle weight		IAGP		N	RGD:5509061	20240307	MGI			PMID:34916661
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20220519	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20201022	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21553379
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21553379
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210128	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210826	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21553379
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21553379
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210128	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20210128	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:21553379
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:21553379
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0005576	decreased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20230601	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0008161	increased diameter of radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0008163	increased diameter of ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21553379
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19097194
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23792766
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20201022	MGI			
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0014106	delayed chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:19465597
1332319	Pkdcc	protein kinase domain containing, cytoplasmic	gene	MP:0021208	median cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:19097194
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20170314	MGI			PMID:26267533
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20230601	MGI			
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20170314	MGI			PMID:26267533
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170314	MGI			PMID:26267533
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20170314	MGI			PMID:26267533
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20170314	MGI			PMID:26267533
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20170314	MGI			PMID:26267533
1332320	Inpp5j	inositol polyphosphate 5-phosphatase J	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20170314	MGI			PMID:26267533
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000103	nasal bone hypoplasia		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20190502	MGI			
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20160218	MGI			PMID:26531099
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26531099
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26531099
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000614	absent salivary gland		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20190502	MGI			
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20160218	MGI			PMID:26531099
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0004197	abnormal fetal growth/weight/body size		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0004352	absent humerus		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20160218	MGI			PMID:26531099
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20160218	MGI			PMID:26531099
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0009893	cleft primary palate		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0013546	cleft soft palate		IAGP		N	RGD:5509061	20160218	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:26371508
1332322	Esrp2	epithelial splicing regulatory protein 2	gene	MP:0031504	increased mouth width		IAGP		N	RGD:5509061	20230810	MGI			PMID:26371508
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637498
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20160811	MGI			
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20251204	MGI			
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20160811	MGI			
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637498
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637498
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637498
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20251204	MGI			
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20637498
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1332323	Srd5a3	steroid 5 alpha-reductase 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0001800	abnormal humoral immune response		IEA		N	RGD:5509061	20200310	MGI			
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0002461	increased immunoglobulin level		IEA		N	RGD:5509061	20200310	MGI			
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0008599	increased circulating interleukin-2 level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0008669	increased interleukin-12b secretion		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332324	Prap1	proline-rich acidic protein 1	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20210506	MGI			PMID:32629119
1332327	Mettl22	methyltransferase 22, Kin17 lysine	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:22560297
1332328	Tmem163	transmembrane protein 163	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:22560297
1332328	Tmem163	transmembrane protein 163	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20170525	MGI			PMID:22560297
1332328	Tmem163	transmembrane protein 163	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1332328	Tmem163	transmembrane protein 163	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1332328	Tmem163	transmembrane protein 163	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20170525	MGI			PMID:24247431
1332328	Tmem163	transmembrane protein 163	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:14676301
1332328	Tmem163	transmembrane protein 163	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20170525	MGI			PMID:14676301
1332328	Tmem163	transmembrane protein 163	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20170525	MGI			PMID:22560297
1332328	Tmem163	transmembrane protein 163	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20170525	MGI			PMID:14676301
1332328	Tmem163	transmembrane protein 163	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20170525	MGI			PMID:24589777
1332328	Tmem163	transmembrane protein 163	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:15975937
1332328	Tmem163	transmembrane protein 163	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:18202285
1332328	Tmem163	transmembrane protein 163	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20170525	MGI			PMID:17360769
1332328	Tmem163	transmembrane protein 163	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20170525	MGI			PMID:15975937
1332328	Tmem163	transmembrane protein 163	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20170525	MGI			PMID:18202285
1332328	Tmem163	transmembrane protein 163	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0001017	abnormal stellate ganglion morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31218818
1332328	Tmem163	transmembrane protein 163	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34977916
1332328	Tmem163	transmembrane protein 163	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20170525	MGI			PMID:17142319
1332328	Tmem163	transmembrane protein 163	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20170525	MGI			PMID:18755802
1332328	Tmem163	transmembrane protein 163	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20170525	MGI			PMID:17142319
1332328	Tmem163	transmembrane protein 163	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20170525	MGI			PMID:17142319
1332328	Tmem163	transmembrane protein 163	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20170525	MGI			PMID:18755802
1332328	Tmem163	transmembrane protein 163	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0001159	absent prostate gland		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180607	MGI			PMID:29222403
1332328	Tmem163	transmembrane protein 163	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170525	MGI			PMID:12724423
1332328	Tmem163	transmembrane protein 163	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170525	MGI			PMID:16287843
1332328	Tmem163	transmembrane protein 163	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170525	MGI			PMID:24247431
1332328	Tmem163	transmembrane protein 163	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170525	MGI			PMID:24589777
1332328	Tmem163	transmembrane protein 163	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170525	MGI			PMID:27053202
1332328	Tmem163	transmembrane protein 163	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20170525	MGI			PMID:17470285
1332328	Tmem163	transmembrane protein 163	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20170525	MGI			PMID:19679071
1332328	Tmem163	transmembrane protein 163	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20180607	MGI			PMID:29222403
1332328	Tmem163	transmembrane protein 163	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20170525	MGI			PMID:14676301
1332328	Tmem163	transmembrane protein 163	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20170525	MGI			PMID:22697126
1332328	Tmem163	transmembrane protein 163	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20170525	MGI			PMID:19679071
1332328	Tmem163	transmembrane protein 163	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20180607	MGI			PMID:29222403
1332328	Tmem163	transmembrane protein 163	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20170525	MGI			PMID:24589777
1332328	Tmem163	transmembrane protein 163	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170525	MGI			PMID:12724423
1332328	Tmem163	transmembrane protein 163	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20170525	MGI			PMID:14676301
1332328	Tmem163	transmembrane protein 163	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20170525	MGI			PMID:24589777
1332328	Tmem163	transmembrane protein 163	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170525	MGI			PMID:18316482
1332328	Tmem163	transmembrane protein 163	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170525	MGI			PMID:18755802
1332328	Tmem163	transmembrane protein 163	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:34977916
1332328	Tmem163	transmembrane protein 163	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20170525	MGI			PMID:18316482
1332328	Tmem163	transmembrane protein 163	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20170525	MGI			PMID:27053202
1332328	Tmem163	transmembrane protein 163	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0001956	hypopnea		IAGP		N	RGD:5509061	20170525	MGI			PMID:27053202
1332328	Tmem163	transmembrane protein 163	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20170525	MGI			PMID:24589777
1332328	Tmem163	transmembrane protein 163	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20231207	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20170525	MGI			PMID:19679071
1332328	Tmem163	transmembrane protein 163	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170525	MGI			PMID:24589777
1332328	Tmem163	transmembrane protein 163	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170525	MGI			PMID:14657014
1332328	Tmem163	transmembrane protein 163	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:17142319
1332328	Tmem163	transmembrane protein 163	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20170525	MGI			PMID:17142319
1332328	Tmem163	transmembrane protein 163	gene	MP:0002669	abnormal scrotum morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20170525	MGI			PMID:18755802
1332328	Tmem163	transmembrane protein 163	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:17470285
1332328	Tmem163	transmembrane protein 163	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20170525	MGI			PMID:17142319
1332328	Tmem163	transmembrane protein 163	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20170525	MGI			PMID:18755802
1332328	Tmem163	transmembrane protein 163	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:17142319
1332328	Tmem163	transmembrane protein 163	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20180607	MGI			PMID:29222403
1332328	Tmem163	transmembrane protein 163	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0003234	enhanced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20180607	MGI			PMID:29222403
1332328	Tmem163	transmembrane protein 163	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20170525	MGI			PMID:12724423
1332328	Tmem163	transmembrane protein 163	gene	MP:0003417	premature endochondral bone ossification		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0003557	absent vas deferens		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20170525	MGI			PMID:18755802
1332328	Tmem163	transmembrane protein 163	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20170525	MGI			PMID:12724423
1332328	Tmem163	transmembrane protein 163	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20220120	MGI			PMID:34931676
1332328	Tmem163	transmembrane protein 163	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20231207	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20170525	MGI			PMID:16287843
1332328	Tmem163	transmembrane protein 163	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:22315402
1332328	Tmem163	transmembrane protein 163	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:22315402
1332328	Tmem163	transmembrane protein 163	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0004218	meiotic nondisjunction during M1 phase		IAGP		N	RGD:5509061	20170525	MGI			PMID:18316482
1332328	Tmem163	transmembrane protein 163	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0004344	scapular bone hypoplasia		IAGP		N	RGD:5509061	20170525	MGI			PMID:22560297
1332328	Tmem163	transmembrane protein 163	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:22560297
1332328	Tmem163	transmembrane protein 163	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20170525	MGI			PMID:22560297
1332328	Tmem163	transmembrane protein 163	gene	MP:0004727	absent epididymis		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:18316482
1332328	Tmem163	transmembrane protein 163	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:18755802
1332328	Tmem163	transmembrane protein 163	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:14676301
1332328	Tmem163	transmembrane protein 163	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20170525	MGI			PMID:18755802
1332328	Tmem163	transmembrane protein 163	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:14676301
1332328	Tmem163	transmembrane protein 163	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:34977916
1332328	Tmem163	transmembrane protein 163	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0005188	small penis		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20170525	MGI			PMID:17470285
1332328	Tmem163	transmembrane protein 163	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20170525	MGI			PMID:27053202
1332328	Tmem163	transmembrane protein 163	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:22560297
1332328	Tmem163	transmembrane protein 163	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20170525	MGI			PMID:27053202
1332328	Tmem163	transmembrane protein 163	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:19679071
1332328	Tmem163	transmembrane protein 163	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20220721	MGI			PMID:33513603
1332328	Tmem163	transmembrane protein 163	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:12724423
1332328	Tmem163	transmembrane protein 163	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20170525	MGI			PMID:17470285
1332328	Tmem163	transmembrane protein 163	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0005575	increased pulmonary ventilation		IAGP		N	RGD:5509061	20170525	MGI			PMID:27053202
1332328	Tmem163	transmembrane protein 163	gene	MP:0005585	increased tidal volume		IAGP		N	RGD:5509061	20170525	MGI			PMID:27053202
1332328	Tmem163	transmembrane protein 163	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20220721	MGI			PMID:33513603
1332328	Tmem163	transmembrane protein 163	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1332328	Tmem163	transmembrane protein 163	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0006295	absent sclerotome		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:17142319
1332328	Tmem163	transmembrane protein 163	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20170525	MGI			PMID:26932671
1332328	Tmem163	transmembrane protein 163	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0008256	abnormal myometrium morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20170525	MGI			PMID:17142319
1332328	Tmem163	transmembrane protein 163	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20170525	MGI			PMID:18316482
1332328	Tmem163	transmembrane protein 163	gene	MP:0008862	asymmetric snout		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20170525	MGI			PMID:15975937
1332328	Tmem163	transmembrane protein 163	gene	MP:0008966	abnormal chiasmata formation		IAGP		N	RGD:5509061	20170525	MGI			PMID:18316482
1332328	Tmem163	transmembrane protein 163	gene	MP:0008984	vagina hypoplasia		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0009066	decreased oviduct weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:14676301
1332328	Tmem163	transmembrane protein 163	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20170525	MGI			PMID:19679071
1332328	Tmem163	transmembrane protein 163	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20180607	MGI			PMID:29222403
1332328	Tmem163	transmembrane protein 163	gene	MP:0009199	abnormal external male genitalia morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0009204	absent external male genitalia		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20170525	MGI			PMID:15919793
1332328	Tmem163	transmembrane protein 163	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20170525	MGI			PMID:19679071
1332328	Tmem163	transmembrane protein 163	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20220721	MGI			PMID:33513603
1332328	Tmem163	transmembrane protein 163	gene	MP:0009736	abnormal prostate gland branching morphogenesis		IAGP		N	RGD:5509061	20170525	MGI			PMID:18755802
1332328	Tmem163	transmembrane protein 163	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20170525	MGI			PMID:27053202
1332328	Tmem163	transmembrane protein 163	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20170525	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1332328	Tmem163	transmembrane protein 163	gene	MP:0010487	abnormal right subclavian artery morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34050709
1332328	Tmem163	transmembrane protein 163	gene	MP:0010709	absent eye anterior chamber		IAGP		N	RGD:5509061	20201119	MGI			PMID:17470285
1332328	Tmem163	transmembrane protein 163	gene	MP:0010734	abnormal paranode morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:20371806
1332328	Tmem163	transmembrane protein 163	gene	MP:0010734	abnormal paranode morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:21632923
1332328	Tmem163	transmembrane protein 163	gene	MP:0010735	abnormal paranodal axoglial junction morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:21632923
1332328	Tmem163	transmembrane protein 163	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:12724423
1332328	Tmem163	transmembrane protein 163	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:24247431
1332328	Tmem163	transmembrane protein 163	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:11316774
1332328	Tmem163	transmembrane protein 163	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:23677977
1332328	Tmem163	transmembrane protein 163	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
1332328	Tmem163	transmembrane protein 163	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:26932671
1332328	Tmem163	transmembrane protein 163	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:16287843
1332328	Tmem163	transmembrane protein 163	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:16287843
1332328	Tmem163	transmembrane protein 163	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:24589777
1332328	Tmem163	transmembrane protein 163	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20241121	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20180607	MGI			PMID:29222403
1332328	Tmem163	transmembrane protein 163	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20170525	MGI			PMID:26932671
1332328	Tmem163	transmembrane protein 163	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0012023	decreased melanocyte number		IAGP		N	RGD:5509061	20170525	MGI			PMID:24247431
1332328	Tmem163	transmembrane protein 163	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20170525	MGI			PMID:21303853
1332328	Tmem163	transmembrane protein 163	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20180607	MGI			PMID:29222403
1332328	Tmem163	transmembrane protein 163	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0012526	abnormal upper rhombic lip morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20170525	MGI			PMID:26932671
1332328	Tmem163	transmembrane protein 163	gene	MP:0012736	abnormal polar body morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34977916
1332328	Tmem163	transmembrane protein 163	gene	MP:0012755	decreased cranial neural crest cell number		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
1332328	Tmem163	transmembrane protein 163	gene	MP:0012761	increased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20230309	MGI			PMID:35593225
1332328	Tmem163	transmembrane protein 163	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:40825043
1332328	Tmem163	transmembrane protein 163	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0013598	Leydig cell hypertrophy		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:18316482
1332328	Tmem163	transmembrane protein 163	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:25201955
1332328	Tmem163	transmembrane protein 163	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0014441	decreased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20170525	MGI			PMID:12370412
1332328	Tmem163	transmembrane protein 163	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1332328	Tmem163	transmembrane protein 163	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20220721	MGI			PMID:33513603
1332328	Tmem163	transmembrane protein 163	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:22697126
1332328	Tmem163	transmembrane protein 163	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:17470285
1332328	Tmem163	transmembrane protein 163	gene	MP:0030143	facial muscle spasm		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1332328	Tmem163	transmembrane protein 163	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:18953638
1332328	Tmem163	transmembrane protein 163	gene	MP:0031334	increased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260618	MGI			PMID:41705663
1332328	Tmem163	transmembrane protein 163	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:29222403
1332328	Tmem163	transmembrane protein 163	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:15919793
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20240502	MGI			PMID:34646989
1332329	Xrn1	5'-3' exoribonuclease 1	gene	MP:0014441	decreased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:34646989
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20200310	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20201231	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20200310	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0005354	abnormal ilium morphology		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0008156	decreased diameter of tibia		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20201231	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0011999	abnormal tail length		IEA		N	RGD:5509061	20201231	MGI			
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0014100	increased chondrocyte proliferation		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332333	Cant1	calcium activated nucleotidase 1	gene	MP:0030848	short ilium		IAGP		N	RGD:5509061	20220512	MGI			PMID:30439444
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427626
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427626
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427626
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20181004	MGI			PMID:29379136
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427626
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427626
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427626
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20181004	MGI			PMID:29379136
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001435	absent suckling reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20181004	MGI			PMID:29379136
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001524	impaired limb coordination		IEA		N	RGD:5509061	20111116	MGI			
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201231	MGI			
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001731	abnormal postnatal growth		IEA		N	RGD:5509061	20111116	MGI			
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427626
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0002200	abnormal brain ventricular system morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427626
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0005113	decreased spinal cord ventral horn cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0005424	jerky movement		IEA		N	RGD:5509061	20111116	MGI			
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20181004	MGI			PMID:29379136
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0009393	abnormal resting posture		IEA		N	RGD:5509061	20111116	MGI			
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20181004	MGI			PMID:29379136
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730604
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240606	MGI			PMID:36933672
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9531547
1332334	Dync1h1	dynein cytoplasmic 1 heavy chain 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1332335	Galnt10	polypeptide N-acetylgalactosaminyltransferase 10	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1332336	Grcc10	gene rich cluster, C10 gene	gene	MP:0001575	cyanosis		IEA		N	RGD:5509061	20210520	MGI			
1332336	Grcc10	gene rich cluster, C10 gene	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332339	Rnaseh2c	ribonuclease H2, subunit C	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20171026	MGI			PMID:22802351
1332339	Rnaseh2c	ribonuclease H2, subunit C	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20150430	MGI			
1332339	Rnaseh2c	ribonuclease H2, subunit C	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20171026	MGI			PMID:22802351
1332339	Rnaseh2c	ribonuclease H2, subunit C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332340	Antkmt	adenine nucleotide translocase lysine methyltransferase	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1332340	Antkmt	adenine nucleotide translocase lysine methyltransferase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1332340	Antkmt	adenine nucleotide translocase lysine methyltransferase	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1332340	Antkmt	adenine nucleotide translocase lysine methyltransferase	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1332340	Antkmt	adenine nucleotide translocase lysine methyltransferase	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1332340	Antkmt	adenine nucleotide translocase lysine methyltransferase	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20210520	MGI			
1332340	Antkmt	adenine nucleotide translocase lysine methyltransferase	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20190808	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20210520	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20190808	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20190808	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20190808	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190808	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20190808	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20190808	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384391
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20190808	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210826	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0009744	postaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668215
1332343	Inpp5e	inositol polyphosphate-5-phosphatase E	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:19668215
1332346	Fam131a	family with sequence similarity 131, member A	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20241121	MGI			
1332347	Mcub	mitochondrial calcium uniporter dominant negative beta subunit	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20190502	MGI			
1332347	Mcub	mitochondrial calcium uniporter dominant negative beta subunit	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20190502	MGI			
1332348	Igf2bp3	insulin-like growth factor 2 mRNA binding protein 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1332348	Igf2bp3	insulin-like growth factor 2 mRNA binding protein 3	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20220811	MGI			
1332349	Rps21	ribosomal protein S21	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1332349	Rps21	ribosomal protein S21	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1332349	Rps21	ribosomal protein S21	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1332349	Rps21	ribosomal protein S21	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1332349	Rps21	ribosomal protein S21	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1332349	Rps21	ribosomal protein S21	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1332349	Rps21	ribosomal protein S21	gene	MP:0009934	abnormal hind foot hair pigmentation		IAGP		N	RGD:5509061	20210930	MGI			PMID:33949947
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024913
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760292
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841208
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543947
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655069
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760292
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266384
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841208
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024913
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543947
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691213
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974039
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207713
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655069
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655069
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691213
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760292
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655069
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841208
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974039
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878804
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878804
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691213
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878804
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207713
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878804
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691213
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760292
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024913
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760292
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002646	increased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760292
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266384
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993927
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992262
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655069
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003192	increased cholesterol efflux		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992262
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003193	decreased cholesterol efflux		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543947
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003193	decreased cholesterol efflux		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992262
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003193	decreased cholesterol efflux		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003981	decreased circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024913
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0004254	cerebral amyloid angiopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207713
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655069
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760292
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266384
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841208
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543947
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691213
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974039
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841208
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005401	abnormal fat-soluble vitamin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655069
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024913
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15163665
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0006084	abnormal circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760292
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0006084	abnormal circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15841208
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20260219	MGI			PMID:17992262
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20260219	MGI			PMID:17992262
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20260219	MGI			PMID:17992262
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0008690	increased interleukin-23 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22862945
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20260219	MGI			PMID:17992262
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992262
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543947
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0009080	uterus inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18160655
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0010161	decreased brain cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878804
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10760292
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691213
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16207713
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0011385	abnormal testosterone level		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:15026428
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:10980140
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0031205	decreased circulating phytosterol level		IAGP		N	RGD:5509061	20210211	MGI			PMID:14699507
1332354	Abca1	ATP-binding cassette, sub-family A member 1	gene	MP:0031632	increased lung cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18160655
1332355	S100g	S100 calcium binding protein G	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:16895982
1332355	S100g	S100 calcium binding protein G	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:17696760
1332355	S100g	S100 calcium binding protein G	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18325990
1332355	S100g	S100 calcium binding protein G	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18325990
1332356	Abra	actin-binding Rho activating protein	gene	MP:0003410	abnormal artery development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778941
1332356	Abra	actin-binding Rho activating protein	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19778941
1332358	Sirt5	sirtuin 5	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22076378
1332358	Sirt5	sirtuin 5	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20260402	MGI			
1332358	Sirt5	sirtuin 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923681
1332358	Sirt5	sirtuin 5	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1332358	Sirt5	sirtuin 5	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200123	MGI			PMID:27681422
1332358	Sirt5	sirtuin 5	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
1332359	Tanc1	tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1332359	Tanc1	tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1332359	Tanc1	tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1332359	Tanc1	tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:21068316
1332359	Tanc1	tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21068316
1332359	Tanc1	tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20181227	MGI			
1332362	Ssx2ip	SSX family member 2 interacting protein	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1332365	Bcdin3d	BCDIN3 domain containing	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20260402	MGI			
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0010134	decreased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22201126
1332366	Zbtb1	zinc finger and BTB domain containing 1	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18676989
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18676989
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210128	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18676989
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18676989
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18676989
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20210826	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0003005	abnormal hippocampal fimbria morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0003006	abnormal hippocampal fornix morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20200310	MGI			PMID:18676989
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210826	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:18676989
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210826	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:23447614
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12904583
1332367	Itsn1	intersectin 1 (SH3 domain protein 1A)	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20210128	MGI			
1332372	Akap11	A kinase anchor protein 11	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1332372	Akap11	A kinase anchor protein 11	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332372	Akap11	A kinase anchor protein 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332372	Akap11	A kinase anchor protein 11	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332372	Akap11	A kinase anchor protein 11	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332372	Akap11	A kinase anchor protein 11	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332372	Akap11	A kinase anchor protein 11	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332372	Akap11	A kinase anchor protein 11	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332372	Akap11	A kinase anchor protein 11	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332372	Akap11	A kinase anchor protein 11	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332372	Akap11	A kinase anchor protein 11	gene	MP:0020211	slow movement		IAGP		N	RGD:5509061	20160929	MGI			PMID:27402760
1332373	Adissp	adipose secreted signaling protein	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0014145	increased white adipose tissue mass		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0020426	abnormal beige fat cell physiology		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332373	Adissp	adipose secreted signaling protein	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20230223	MGI			PMID:36496438
1332374	Exoc3	exocyst complex component 3	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20210325	MGI			PMID:33560379
1332374	Exoc3	exocyst complex component 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1332374	Exoc3	exocyst complex component 3	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20210325	MGI			PMID:33560379
1332374	Exoc3	exocyst complex component 3	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33560379
1332374	Exoc3	exocyst complex component 3	gene	MP:0005607	decreased bleeding time		IAGP		N	RGD:5509061	20210325	MGI			PMID:33560379
1332374	Exoc3	exocyst complex component 3	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20210325	MGI			PMID:33560379
1332374	Exoc3	exocyst complex component 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1332374	Exoc3	exocyst complex component 3	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1332374	Exoc3	exocyst complex component 3	gene	MP:0020965	increased platelet dense granule secretion		IAGP		N	RGD:5509061	20210325	MGI			PMID:33560379
1332374	Exoc3	exocyst complex component 3	gene	MP:0020966	decreased platelet dense granule secretion		IAGP		N	RGD:5509061	20210325	MGI			PMID:33560379
1332374	Exoc3	exocyst complex component 3	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20210325	MGI			PMID:33560379
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0000537	abnormal urethra morphology		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0011485	abnormal urethra urothelium morphology		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332375	Olah	oleoyl-ACP hydrolase	gene	MP:0031045	decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20241010	MGI			PMID:39137778
1332378	Hemgn	hemogen	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20220804	MGI			PMID:35297980
1332378	Hemgn	hemogen	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1332378	Hemgn	hemogen	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20220804	MGI			PMID:35297980
1332378	Hemgn	hemogen	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20220804	MGI			PMID:35297980
1332378	Hemgn	hemogen	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1332378	Hemgn	hemogen	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20220804	MGI			PMID:35297980
1332379	Lmf1	lipase maturation factor 1	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20151015	MGI			PMID:25302068
1332379	Lmf1	lipase maturation factor 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20151015	MGI			PMID:25302068
1332379	Lmf1	lipase maturation factor 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1332379	Lmf1	lipase maturation factor 1	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20151015	MGI			PMID:25302068
1332379	Lmf1	lipase maturation factor 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0009699	hyperchylomicronemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151015	MGI			PMID:25302068
1332379	Lmf1	lipase maturation factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1332379	Lmf1	lipase maturation factor 1	gene	MP:0011579	decreased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:3972797
1332379	Lmf1	lipase maturation factor 1	gene	MP:0011579	decreased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0011579	decreased lipoprotein lipase activity		IAGP		N	RGD:5509061	20151015	MGI			PMID:25302068
1332379	Lmf1	lipase maturation factor 1	gene	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:6857276
1332379	Lmf1	lipase maturation factor 1	gene	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20151015	MGI			PMID:25302068
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0004036	abnormal muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0004089	dilated sarcoplasmic reticulum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465920
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20220609	MGI			PMID:30412589
1332381	Mtmr14	myotubularin related protein 14	gene	MP:0014915	decreased muscle cell calcium uptake		IAGP		N	RGD:5509061	20260219	MGI			PMID:19465920
1332387	Patl1	protein associated with topoisomerase II homolog 1 (yeast)	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1332387	Patl1	protein associated with topoisomerase II homolog 1 (yeast)	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20190502	MGI			
1332387	Patl1	protein associated with topoisomerase II homolog 1 (yeast)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1332387	Patl1	protein associated with topoisomerase II homolog 1 (yeast)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332387	Patl1	protein associated with topoisomerase II homolog 1 (yeast)	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1332388	Kifc2	kinesin family member C2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1332388	Kifc2	kinesin family member C2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:11259594
1332389	Adprm	ADP-ribose/CDP-alcohol diphosphatase, manganese dependent	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210128	MGI			
1332389	Adprm	ADP-ribose/CDP-alcohol diphosphatase, manganese dependent	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1332389	Adprm	ADP-ribose/CDP-alcohol diphosphatase, manganese dependent	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1332389	Adprm	ADP-ribose/CDP-alcohol diphosphatase, manganese dependent	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1332389	Adprm	ADP-ribose/CDP-alcohol diphosphatase, manganese dependent	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20260402	MGI			
1332389	Adprm	ADP-ribose/CDP-alcohol diphosphatase, manganese dependent	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201231	MGI			
1332389	Adprm	ADP-ribose/CDP-alcohol diphosphatase, manganese dependent	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20211021	MGI			
1332389	Adprm	ADP-ribose/CDP-alcohol diphosphatase, manganese dependent	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1332390	Fam216a	family with sequence similarity 216, member A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1332390	Fam216a	family with sequence similarity 216, member A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20181227	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1332391	Pkig	protein kinase inhibitor, gamma	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1332393	Fstl1	follistatin-like 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20210520	MGI			
1332393	Fstl1	follistatin-like 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21382556
1332393	Fstl1	follistatin-like 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1332393	Fstl1	follistatin-like 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0001942	abnormal lung volume		IAGP		N	RGD:5509061	20220407	MGI			PMID:31834999
1332393	Fstl1	follistatin-like 1	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20220407	MGI			PMID:31834999
1332393	Fstl1	follistatin-like 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20220407	MGI			PMID:31834999
1332393	Fstl1	follistatin-like 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:20861081
1332393	Fstl1	follistatin-like 1	gene	MP:0002249	abnormal larynx morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0002738	hyperresponsive to tactile stimuli		IAGP		N	RGD:5509061	20200310	MGI			PMID:21382556
1332393	Fstl1	follistatin-like 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0003588	ureter stenosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0003856	abnormal hindlimb stylopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:21382556
1332393	Fstl1	follistatin-like 1	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0004202	pulmonary hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0004372	bowed fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0004551	decreased tracheal cartilage ring number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0004694	absent patella		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1332393	Fstl1	follistatin-like 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1332393	Fstl1	follistatin-like 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1332393	Fstl1	follistatin-like 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:21382556
1332393	Fstl1	follistatin-like 1	gene	MP:0005440	increased glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0006432	abnormal costal cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0008532	decreased chemical nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:21382556
1332393	Fstl1	follistatin-like 1	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21987816
1332393	Fstl1	follistatin-like 1	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0010816	decreased type I pneumocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0010883	trachea stenosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20220407	MGI			PMID:31834999
1332393	Fstl1	follistatin-like 1	gene	MP:0010902	abnormal pulmonary alveolar sac morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0010950	abnormal lung hysteresivity		IAGP		N	RGD:5509061	20220407	MGI			PMID:31834999
1332393	Fstl1	follistatin-like 1	gene	MP:0010975	abnormal lung lobe morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0011045	decreased lung elastance		IAGP		N	RGD:5509061	20220407	MGI			PMID:31834999
1332393	Fstl1	follistatin-like 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482757
1332393	Fstl1	follistatin-like 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0011304	kidney papillary atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0011484	abnormal ureter urothelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22485132
1332393	Fstl1	follistatin-like 1	gene	MP:0011505	camptomelia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1332393	Fstl1	follistatin-like 1	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:21382556
1332393	Fstl1	follistatin-like 1	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0030002	increased lung apoptosis		IAGP		N	RGD:5509061	20220407	MGI			PMID:31834999
1332393	Fstl1	follistatin-like 1	gene	MP:0030859	absent sesamoid bone of gastrocnemius		IAGP		N	RGD:5509061	20200310	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:21826198
1332393	Fstl1	follistatin-like 1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:21987816
1332397	Ndufaf6	NADH:ubiquinone oxidoreductase complex assembly factor 6	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1332398	Adap1	ArfGAP with dual PH domains 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20230126	MGI			PMID:33139322
1332398	Adap1	ArfGAP with dual PH domains 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:31792062
1332398	Adap1	ArfGAP with dual PH domains 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20230126	MGI			PMID:33139322
1332398	Adap1	ArfGAP with dual PH domains 1	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1332398	Adap1	ArfGAP with dual PH domains 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20230126	MGI			PMID:33139322
1332398	Adap1	ArfGAP with dual PH domains 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20230126	MGI			PMID:33139322
1332398	Adap1	ArfGAP with dual PH domains 1	gene	MP:0013426	decreased memory-marker NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1332398	Adap1	ArfGAP with dual PH domains 1	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20230126	MGI			PMID:33139322
1332398	Adap1	ArfGAP with dual PH domains 1	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20230126	MGI			PMID:33139322
1332399	Bco1	beta-carotene oxygenase 1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855355
1332399	Bco1	beta-carotene oxygenase 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855355
1332399	Bco1	beta-carotene oxygenase 1	gene	MP:0004019	abnormal vitamin homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855355
1332399	Bco1	beta-carotene oxygenase 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855355
1332399	Bco1	beta-carotene oxygenase 1	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855355
1332399	Bco1	beta-carotene oxygenase 1	gene	MP:0011232	abnormal vitamin A level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855355
1332399	Bco1	beta-carotene oxygenase 1	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:17855355
1332400	Rnf43	ring finger protein 43	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20200423	MGI			PMID:30884828
1332400	Rnf43	ring finger protein 43	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22895187
1332400	Rnf43	ring finger protein 43	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0002814	hyperchromasia		IAGP		N	RGD:5509061	20200423	MGI			PMID:30884828
1332400	Rnf43	ring finger protein 43	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:30884828
1332400	Rnf43	ring finger protein 43	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22895187
1332400	Rnf43	ring finger protein 43	gene	MP:0005213	gastric metaplasia		IAGP		N	RGD:5509061	20200423	MGI			PMID:30884828
1332400	Rnf43	ring finger protein 43	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200423	MGI			PMID:30884828
1332400	Rnf43	ring finger protein 43	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230119	MGI			
1332400	Rnf43	ring finger protein 43	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22895187
1332400	Rnf43	ring finger protein 43	gene	MP:0010783	abnormal stomach wall morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:30380024
1332400	Rnf43	ring finger protein 43	gene	MP:0010783	abnormal stomach wall morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:30884828
1332400	Rnf43	ring finger protein 43	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:30380024
1332400	Rnf43	ring finger protein 43	gene	MP:0013485	increased Paneth cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:22895187
1332400	Rnf43	ring finger protein 43	gene	MP:0013578	abnormal stomach glandular region morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:30380024
1332402	Fam81a	family with sequence similarity 81, member A	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1332402	Fam81a	family with sequence similarity 81, member A	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1332402	Fam81a	family with sequence similarity 81, member A	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220519	MGI			
1332402	Fam81a	family with sequence similarity 81, member A	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1332402	Fam81a	family with sequence similarity 81, member A	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1332402	Fam81a	family with sequence similarity 81, member A	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1332403	Anks3	ankyrin repeat and sterile alpha motif domain containing 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200310	MGI			
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20230601	MGI			
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0004388	absent prechordal plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20230601	MGI			
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0012517	absent diencephalon		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0012683	absent telencephalon		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0013185	absent anterior definitive endoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332404	Cnbp	cellular nucleic acid binding protein	gene	MP:0013505	decreased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12588852
1332405	Tmem87a	transmembrane protein 87A	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
1332405	Tmem87a	transmembrane protein 87A	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1332405	Tmem87a	transmembrane protein 87A	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20240404	MGI			PMID:38422143
1332405	Tmem87a	transmembrane protein 87A	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20240404	MGI			PMID:38422143
1332405	Tmem87a	transmembrane protein 87A	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20250508	MGI			
1332405	Tmem87a	transmembrane protein 87A	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1332405	Tmem87a	transmembrane protein 87A	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20240404	MGI			PMID:38422143
1332405	Tmem87a	transmembrane protein 87A	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20250508	MGI			
1332405	Tmem87a	transmembrane protein 87A	gene	MP:0010055	abnormal sensory neuron physiology		IAGP		N	RGD:5509061	20240404	MGI			PMID:38422143
1332406	Mnd1	meiotic nuclear divisions 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24304900
1332406	Mnd1	meiotic nuclear divisions 1	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24304900
1332406	Mnd1	meiotic nuclear divisions 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24304900
1332406	Mnd1	meiotic nuclear divisions 1	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:24304900
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1332407	Ciao2b	cytosolic iron-sulfur assembly component 2B	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1332408	Mri1	methylthioribose-1-phosphate isomerase 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230601	MGI			
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332409	Guf1	GUF1 homolog, GTPase	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20230316	MGI			PMID:27065197
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15473967
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15473967
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0000821	choroid plexus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673330
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0000923	abnormal roof plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673330
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673330
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15473967
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:15473967
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673330
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673330
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23673330
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15473967
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0014553	decreased neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:15473967
1332410	Nde1	nudE neurodevelopment protein 1	gene	MP:0021091	abnormal dorsal interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:23673330
1332414	Gid8	GID complex subunit 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20181004	MGI			PMID:25753038
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879509
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20181004	MGI			PMID:25753038
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0011922	abnormal circulating osteocalcin level		IAGP		N	RGD:5509061	20181004	MGI			PMID:25753038
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0031117	subdural hemorrhage		IAGP		N	RGD:5509061	20200917	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0031136	muscle hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:19492146
1332416	Vkorc1	vitamin K epoxide reductase complex, subunit 1	gene	MP:0031152	subcutaneous hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:19492146
1332417	Tmt1b	thiol methyltransferase 1B	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20230720	MGI			
1332417	Tmt1b	thiol methyltransferase 1B	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20230720	MGI			
1332417	Tmt1b	thiol methyltransferase 1B	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20230720	MGI			
1332417	Tmt1b	thiol methyltransferase 1B	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20260402	MGI			
1332419	Emc6	ER membrane protein complex subunit 6	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20231207	MGI			
1332419	Emc6	ER membrane protein complex subunit 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332419	Emc6	ER membrane protein complex subunit 6	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1332419	Emc6	ER membrane protein complex subunit 6	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20180308	MGI			PMID:27671655
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20180308	MGI			PMID:27671655
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0004807	abnormal paired-pulse inhibition		IAGP		N	RGD:5509061	20180308	MGI			PMID:27671655
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20180308	MGI			PMID:27671655
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20240523	MGI			
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20240523	MGI			
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1332420	Tspoap1	TSPO associated protein 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1332421	Galnt13	polypeptide N-acetylgalactosaminyltransferase 13	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1332421	Galnt13	polypeptide N-acetylgalactosaminyltransferase 13	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1332421	Galnt13	polypeptide N-acetylgalactosaminyltransferase 13	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220519	MGI			
1332421	Galnt13	polypeptide N-acetylgalactosaminyltransferase 13	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
1332421	Galnt13	polypeptide N-acetylgalactosaminyltransferase 13	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1332421	Galnt13	polypeptide N-acetylgalactosaminyltransferase 13	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1332421	Galnt13	polypeptide N-acetylgalactosaminyltransferase 13	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1332421	Galnt13	polypeptide N-acetylgalactosaminyltransferase 13	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1332421	Galnt13	polypeptide N-acetylgalactosaminyltransferase 13	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20201022	MGI			
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20161103	MGI			PMID:26247364
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161103	MGI			PMID:26247364
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20161103	MGI			PMID:26247364
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20160421	MGI			
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20161103	MGI			PMID:26247364
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20161103	MGI			PMID:26247364
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20160421	MGI			
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20181227	MGI			
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20161103	MGI			PMID:26247364
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20161103	MGI			PMID:26247364
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20161103	MGI			PMID:26247364
1332422	Camkmt	calmodulin-lysine N-methyltransferase	gene	MP:0021165	behavioral developmental delay		IAGP		N	RGD:5509061	20220922	MGI			PMID:26247364
1332425	Tmem175	transmembrane protein 175	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1332425	Tmem175	transmembrane protein 175	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210826	MGI			
1332425	Tmem175	transmembrane protein 175	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1332425	Tmem175	transmembrane protein 175	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1332425	Tmem175	transmembrane protein 175	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0008407	decreased cellular sensitivity to hydrogen peroxide		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20210506	MGI			PMID:33505021
1332425	Tmem175	transmembrane protein 175	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1332425	Tmem175	transmembrane protein 175	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1332425	Tmem175	transmembrane protein 175	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20260402	MGI			
1332427	Septin3	septin 3	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1332427	Septin3	septin 3	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20211021	MGI			
1332427	Septin3	septin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10446280
1332427	Septin3	septin 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332428	Ca4	carbonic anhydrase 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260723
1332428	Ca4	carbonic anhydrase 4	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260723
1332428	Ca4	carbonic anhydrase 4	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260723
1332428	Ca4	carbonic anhydrase 4	gene	MP:0004043	abnormal pH regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260723
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20220811	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20220811	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20241121	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230406	MGI			PMID:33188300
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220811	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20230406	MGI			PMID:33188300
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20230406	MGI			PMID:33188300
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20230406	MGI			PMID:33188300
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20230406	MGI			PMID:33188300
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220811	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230406	MGI			PMID:33188300
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1332429	Hpdl	4-hydroxyphenylpyruvate dioxygenase-like	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1332432	Odad1	outer dynein arm docking complex subunit 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200514	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20200514	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20200514	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20241121	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20200514	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20210520	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0009138	increased brown fat lipid droplet number		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20180322	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0013676	increased Ly6C-positive mature NK cell number		IEA		N	RGD:5509061	20210826	MGI			
1332433	Cluh	clustered mitochondria homolog	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0030644	increased circulating methionine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0030667	increased circulating proline level		IAGP		N	RGD:5509061	20180920	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0030694	increased circulating serine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0030703	increased circulating threonine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:28188211
1332433	Cluh	clustered mitochondria homolog	gene	MP:0030718	increased circulating lysine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:28188211
1332434	Plekho2	pleckstrin homology domain containing O2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20191024	MGI			PMID:28627369
1332434	Plekho2	pleckstrin homology domain containing O2	gene	MP:0011080	increased macrophage apoptosis		IAGP		N	RGD:5509061	20191024	MGI			PMID:28627369
1332436	Sgsm3	small G protein signaling modulator 3	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1332436	Sgsm3	small G protein signaling modulator 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1332439	Arfgef2	ARF guanine nucleotide exchange factor 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22956851
1332439	Arfgef2	ARF guanine nucleotide exchange factor 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22956851
1332439	Arfgef2	ARF guanine nucleotide exchange factor 2	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22956851
1332439	Arfgef2	ARF guanine nucleotide exchange factor 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22956851
1332439	Arfgef2	ARF guanine nucleotide exchange factor 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20857375
1332439	Arfgef2	ARF guanine nucleotide exchange factor 2	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20141003	MGI			PMID:22956851
1332441	Rtca	RNA 3'-terminal phosphate cyclase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161124	MGI			PMID:25961792
1332441	Rtca	RNA 3'-terminal phosphate cyclase	gene	MP:0030013	enhanced central nervous system regeneration		IAGP		N	RGD:5509061	20170713	MGI			PMID:25961792
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724128
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20190502	MGI			
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724128
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724128
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23515163
1332442	Trib1	tribbles pseudokinase 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332446	Mss51	MSS51 mitochondrial translational activator	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20191205	MGI			PMID:29913553
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493085
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159799
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11911824
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002148	abnormal hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002194	maximal tonic hindlimb extension seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159799
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8552190
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8552190
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109709
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8552190
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8552190
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10981970
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12528127
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109709
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21159799
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109709
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17446931
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109709
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17435165
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18949059
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8552190
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008121	increased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109709
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109709
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8552190
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8552190
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8552190
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109709
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8552190
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23123062
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23109709
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0009646	urinary bladder inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22432050
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0011508	abnormal glomerular capillary thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21724994
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:23109709
1332447	Fcgr2b	Fc receptor, IgG, low affinity IIb	gene	MP:0020993	abnormal urine cytokine level		IAGP		N	RGD:5509061	20210408	MGI			PMID:22432050
1332449	Ogfod3	2-oxoglutarate and iron-dependent oxygenase domain containing 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20170105	MGI			
1332449	Ogfod3	2-oxoglutarate and iron-dependent oxygenase domain containing 3	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20190502	MGI			
1332449	Ogfod3	2-oxoglutarate and iron-dependent oxygenase domain containing 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0030934	decreased primordial germ cell proliferation		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332450	Faap100	Fanconi anemia core complex associated protein 100	gene	MP:0030935	increased primordial germ cell apoptosis		IAGP		N	RGD:5509061	20231130	MGI			PMID:37580696
1332452	Rasd2	RASD family, member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199135
1332452	Rasd2	RASD family, member 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199135
1332452	Rasd2	RASD family, member 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199135
1332452	Rasd2	RASD family, member 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199135
1332452	Rasd2	RASD family, member 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199135
1332453	Ctsm	cathepsin M	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1332453	Ctsm	cathepsin M	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1332453	Ctsm	cathepsin M	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20181227	MGI			
1332453	Ctsm	cathepsin M	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20201022	MGI			
1332453	Ctsm	cathepsin M	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469635
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469635
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180201	MGI			PMID:19503083
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180201	MGI			PMID:23936174
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23936174
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469635
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20180201	MGI			PMID:19503083
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20180201	MGI			PMID:23936174
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19503083
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0003267	constipation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23936174
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20180201	MGI			PMID:19503083
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23936174
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:19503083
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20180201	MGI			PMID:23936174
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19503083
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20180201	MGI			PMID:19503083
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20180201	MGI			PMID:23455607
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20180201	MGI			PMID:23455607
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469635
1332454	Khdrbs2	KH domain containing, RNA binding, signal transduction associated 2	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:24469635
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:12649138
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12649138
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19218085
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19218085
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0005074	impaired granulocyte bactericidal activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:12649138
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:12649138
1332455	Pglyrp1	peptidoglycan recognition protein 1	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20709292
1332458	Daglb	diacylglycerol lipase, beta	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147530
1332458	Daglb	diacylglycerol lipase, beta	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807615
1332458	Daglb	diacylglycerol lipase, beta	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20147530
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0004659	abnormal odontoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17266133
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21059868
1332459	Mtf2	metal response element binding transcription factor 2	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20180125	MGI			PMID:17266133
1332461	Snap47	synaptosomal-associated protein, 47	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1332461	Snap47	synaptosomal-associated protein, 47	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20150108	MGI			
1332461	Snap47	synaptosomal-associated protein, 47	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1332461	Snap47	synaptosomal-associated protein, 47	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1332461	Snap47	synaptosomal-associated protein, 47	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20181227	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0000579	abnormal nail morphology		IEA		N	RGD:5509061	20181227	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210520	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055941
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20181227	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20241121	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055941
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055941
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055941
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23055941
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1332463	Rabl2	RAB, member RAS oncogene family-like 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0004974	decreased regulatory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20201231	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0008126	increased dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0008127	decreased dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0008186	increased pro-B cell number		IEA		N	RGD:5509061	20201231	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844206
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0013430	increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0013649	decreased CD11b-high dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0013651	increased CD11b-low dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0013666	decreased immature NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1332466	Pclaf	PCNA clamp associated factor	gene	MP:0013673	increased mature NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20190502	MGI			
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20200402	MGI			
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20240523	MGI			
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20230601	MGI			
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0012017	grizzled coat color		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0012065	increased astrocyte number		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332470	Taco1	translational activator of mitochondrially encoded cytochrome c oxidase I	gene	MP:0020434	increased astrocyte size		IAGP		N	RGD:5509061	20170810	MGI			PMID:27319982
1332476	Wdr83	WD repeat domain containing 83	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726548
1332476	Wdr83	WD repeat domain containing 83	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726548
1332476	Wdr83	WD repeat domain containing 83	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726548
1332476	Wdr83	WD repeat domain containing 83	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726548
1332476	Wdr83	WD repeat domain containing 83	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726548
1332476	Wdr83	WD repeat domain containing 83	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726548
1332476	Wdr83	WD repeat domain containing 83	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726548
1332476	Wdr83	WD repeat domain containing 83	gene	MP:0011372	decreased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726548
1332478	Heatr3	HEAT repeat containing 3	gene	MP:0003443	increased circulating glycerol level		IEA		N	RGD:5509061	20160804	MGI			
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20200402	MGI			
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0004043	abnormal pH regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165320
1332479	Slc4a10	solute carrier family 4, sodium bicarbonate cotransporter-like, member 10	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1332480	Ak8	adenylate kinase 8	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1332480	Ak8	adenylate kinase 8	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1332480	Ak8	adenylate kinase 8	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0000126	brittle teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0000525	renal tubular acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001765	abnormal ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002318	hypercapnia		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003016	increased circulating bicarbonate level		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26224717
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003030	acidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003267	constipation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20200310	MGI			PMID:26224717
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0005634	decreased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20200310	MGI			PMID:26224717
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009477	small cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009478	coiled cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009644	uremia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0011504	abnormal limb long bone morphology		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0011736	decreased urine ammonia level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26224717
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0012549	hypoxemia		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0012550	respiratory acidosis		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20170921	MGI			PMID:21228764
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26224717
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0014350	disorganized spleen B cell follicle		IAGP		N	RGD:5509061	20240104	MGI			PMID:17192275
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20260528	MGI			PMID:31040187
1332483	Slc4a4	solute carrier family 4 (anion exchanger), member 4	gene	MP:0030604	abnormal ammonia homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26224717
1332485	Vars2	valyl-tRNA synthetase 2, mitochondrial	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20190502	MGI			
1332485	Vars2	valyl-tRNA synthetase 2, mitochondrial	gene	MP:0003394	increased cardiac output		IEA		N	RGD:5509061	20211021	MGI			
1332485	Vars2	valyl-tRNA synthetase 2, mitochondrial	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332485	Vars2	valyl-tRNA synthetase 2, mitochondrial	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792318
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792318
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792318
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792318
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792318
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869368
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792318
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170223	MGI			PMID:27134141
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792318
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869368
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20250508	MGI			
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792318
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0008274	failure of bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869368
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0008275	failure of endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869368
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0010936	decreased airway resistance		IEA		N	RGD:5509061	20260402	MGI			
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11792318
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16203988
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20250508	MGI			
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0020080	increased bone mineralization		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0021030	decreased tumor necrosis factor (ligand) superfamily member 11 level		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332486	Sp7	Sp7 transcription factor 7	gene	MP:0031008	decreased bone marrow adipose tissue amount		IAGP		N	RGD:5509061	20250911	MGI			PMID:38346941
1332487	Nyap1	neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20180118	MGI			PMID:21946561
1332487	Nyap1	neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1332487	Nyap1	neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20180118	MGI			PMID:21946561
1332487	Nyap1	neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 1	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:21946561
1332488	Zfp438	zinc finger protein 438	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1332491	Cfap36	cilia and flagella associated protein 36	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1332491	Cfap36	cilia and flagella associated protein 36	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1332491	Cfap36	cilia and flagella associated protein 36	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160804	MGI			
1332492	Tmem131l	transmembrane 131 like	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220519	MGI			
1332492	Tmem131l	transmembrane 131 like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332494	Ccdc51	coiled-coil domain containing 51	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20191114	MGI			PMID:31435016
1332494	Ccdc51	coiled-coil domain containing 51	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1332494	Ccdc51	coiled-coil domain containing 51	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:31435016
1332494	Ccdc51	coiled-coil domain containing 51	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1332497	Egfl7	EGF-like domain 7	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626061
1332497	Egfl7	EGF-like domain 7	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626061
1332497	Egfl7	EGF-like domain 7	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626061
1332497	Egfl7	EGF-like domain 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18987025
1332497	Egfl7	EGF-like domain 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9986727
1332497	Egfl7	EGF-like domain 7	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626061
1332497	Egfl7	EGF-like domain 7	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626061
1332497	Egfl7	EGF-like domain 7	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626061
1332497	Egfl7	EGF-like domain 7	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626061
1332497	Egfl7	EGF-like domain 7	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626061
1332498	Dlgap1	DLG associated protein 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20190502	MGI			
1332498	Dlgap1	DLG associated protein 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20180913	MGI			PMID:29396406
1332498	Dlgap1	DLG associated protein 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1332498	Dlgap1	DLG associated protein 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1332498	Dlgap1	DLG associated protein 1	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20180913	MGI			PMID:29396406
1332498	Dlgap1	DLG associated protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20190502	MGI			
1332498	Dlgap1	DLG associated protein 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20190502	MGI			
1332498	Dlgap1	DLG associated protein 1	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20180913	MGI			PMID:29396406
1332498	Dlgap1	DLG associated protein 1	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20190502	MGI			
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:31661432
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20170323	MGI			
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:31661432
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0001577	anemia		IEA		N	RGD:5509061	20170323	MGI			
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0001790	abnormal immune system physiology		IEA		N	RGD:5509061	20170323	MGI			
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20170323	MGI			
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170323	MGI			
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:31661432
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24487409
1332499	Glmp	glycosylated lysosomal membrane protein	gene	MP:0031148	abnormal liver sinusoidal endothelial cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31661432
1332500	Myod1	myogenic differentiation 1	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
1332500	Myod1	myogenic differentiation 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
1332500	Myod1	myogenic differentiation 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11060232
1332500	Myod1	myogenic differentiation 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1332500	Myod1	myogenic differentiation 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212806
1332500	Myod1	myogenic differentiation 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17961534
1332500	Myod1	myogenic differentiation 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
1332500	Myod1	myogenic differentiation 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14732408
1332500	Myod1	myogenic differentiation 1	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
1332500	Myod1	myogenic differentiation 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
1332500	Myod1	myogenic differentiation 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239359
1332500	Myod1	myogenic differentiation 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239359
1332500	Myod1	myogenic differentiation 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1332500	Myod1	myogenic differentiation 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
1332500	Myod1	myogenic differentiation 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17028574
1332500	Myod1	myogenic differentiation 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17028574
1332500	Myod1	myogenic differentiation 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:1330322
1332500	Myod1	myogenic differentiation 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
1332500	Myod1	myogenic differentiation 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
1332500	Myod1	myogenic differentiation 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
1332500	Myod1	myogenic differentiation 1	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1332500	Myod1	myogenic differentiation 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
1332500	Myod1	myogenic differentiation 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
1332500	Myod1	myogenic differentiation 1	gene	MP:0004846	absent skeletal muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1332500	Myod1	myogenic differentiation 1	gene	MP:0004846	absent skeletal muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
1332500	Myod1	myogenic differentiation 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
1332500	Myod1	myogenic differentiation 1	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9874799
1332500	Myod1	myogenic differentiation 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212806
1332500	Myod1	myogenic differentiation 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386014
1332500	Myod1	myogenic differentiation 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10694423
1332500	Myod1	myogenic differentiation 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9609818
1332500	Myod1	myogenic differentiation 1	gene	MP:0030957	abnormal myotube morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:11060232
1332500	Myod1	myogenic differentiation 1	gene	MP:0031328	delayed skeletal muscle regeneration		IAGP		N	RGD:5509061	20220106	MGI			PMID:17028574
1332502	Slc46a3	solute carrier family 46, member 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210520	MGI			
1332502	Slc46a3	solute carrier family 46, member 3	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20160421	MGI			
1332502	Slc46a3	solute carrier family 46, member 3	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1332502	Slc46a3	solute carrier family 46, member 3	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1332502	Slc46a3	solute carrier family 46, member 3	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220519	MGI			
1332502	Slc46a3	solute carrier family 46, member 3	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20210128	MGI			
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0003926	decreased cellular glucose uptake		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20250918	MGI			PMID:31105056
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0020868	decreased lipogenesis		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0030020	decreased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332503	Abhd15	abhydrolase domain containing 15	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20250911	MGI			PMID:29768196
1332505	Unc119	unc-119 lipid binding chaperone	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210805	MGI			
1332505	Unc119	unc-119 lipid binding chaperone	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210805	MGI			
1332505	Unc119	unc-119 lipid binding chaperone	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174953
1332505	Unc119	unc-119 lipid binding chaperone	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174953
1332505	Unc119	unc-119 lipid binding chaperone	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174953
1332505	Unc119	unc-119 lipid binding chaperone	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174953
1332505	Unc119	unc-119 lipid binding chaperone	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174953
1332505	Unc119	unc-119 lipid binding chaperone	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:17174953
1332506	Gins3	GINS complex subunit 3	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20230504	MGI			PMID:35603789
1332506	Gins3	GINS complex subunit 3	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20230504	MGI			PMID:35603789
1332506	Gins3	GINS complex subunit 3	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20230504	MGI			PMID:35603789
1332506	Gins3	GINS complex subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200514	MGI			
1332506	Gins3	GINS complex subunit 3	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20230504	MGI			PMID:35603789
1332506	Gins3	GINS complex subunit 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1332506	Gins3	GINS complex subunit 3	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20230504	MGI			PMID:35603789
1332509	Rpl3	ribosomal protein L3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230601	MGI			PMID:37080962
1332510	Qrfpr	pyroglutamylated RFamide peptide receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382160
1332510	Qrfpr	pyroglutamylated RFamide peptide receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382160
1332510	Qrfpr	pyroglutamylated RFamide peptide receptor	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382160
1332510	Qrfpr	pyroglutamylated RFamide peptide receptor	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382160
1332510	Qrfpr	pyroglutamylated RFamide peptide receptor	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382160
1332510	Qrfpr	pyroglutamylated RFamide peptide receptor	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20250102	MGI			PMID:36251705
1332510	Qrfpr	pyroglutamylated RFamide peptide receptor	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382160
1332510	Qrfpr	pyroglutamylated RFamide peptide receptor	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382160
1332510	Qrfpr	pyroglutamylated RFamide peptide receptor	gene	MP:0006392	abnormal nucleus pulposus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382160
1332511	Sybu	syntabulin (syntaxin-interacting)	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20201022	MGI			
1332511	Sybu	syntabulin (syntaxin-interacting)	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20201022	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210826	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20230601	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733033
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151126	MGI			PMID:21779371
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733033
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733033
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21779371
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002467	impaired neutrophil phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733033
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240627	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220519	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21779371
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733033
1332512	Padi4	peptidyl arginine deiminase, type IV	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:21779371
1332513	Lsg1	large 60S subunit nuclear export GTPase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210520	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20201224	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0005607	decreased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0010613	abnormal mitral valve annulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0010621	abnormal tricuspid valve annulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24278323
1332514	Pdlim7	PDZ and LIM domain 7	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:24278323
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20240523	MGI			
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20240523	MGI			
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220519	MGI			
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210128	MGI			
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20220519	MGI			
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20211216	MGI			PMID:33303946
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20211216	MGI			PMID:33303946
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20211216	MGI			PMID:33303946
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20220519	MGI			
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20211216	MGI			PMID:33303946
1332515	Zfp804a	zinc finger protein 804A	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20211216	MGI			PMID:33303946
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20230601	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20210520	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20141003	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000927	small floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20200514	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20200514	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20230601	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003321	tracheoesophageal fistula		IEA		N	RGD:5509061	20141003	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20230601	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20220519	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003761	arched palate		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003817	abnormal pituitary diverticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0003924	diaphragmatic hernia		IEA		N	RGD:5509061	20141003	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20141003	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0006130	pulmonary valve atresia		IEA		N	RGD:5509061	20141003	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0008480	absent eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20220519	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0011674	multiple major aortopulmonary collateral arteries		IEA		N	RGD:5509061	20141003	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20141003	MGI			
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767740
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0013264	tongue ankylosis		IAGP		N	RGD:5509061	20221027	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0013550	abnormal secondary palate morphology		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:19877275
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20220721	MGI			PMID:21935430
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0030345	enlarged maxillary prominence		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1332516	Fuz	fuzzy planar cell polarity protein	gene	MP:0030373	Meckel's cartilage hyperplasia		IAGP		N	RGD:5509061	20171207	MGI			PMID:21935430
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230720	MGI			
1332517	Atp5mk	ATP synthase membrane subunit k	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20230720	MGI			
1332519	Cep89	centrosomal protein 89	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1332519	Cep89	centrosomal protein 89	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1332519	Cep89	centrosomal protein 89	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20250508	MGI			
1332519	Cep89	centrosomal protein 89	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20250508	MGI			
1332519	Cep89	centrosomal protein 89	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1332519	Cep89	centrosomal protein 89	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20250508	MGI			
1332519	Cep89	centrosomal protein 89	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20250508	MGI			
1332524	Utp6	UTP6 small subunit processome component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1332525	Slc6a7	solute carrier family 6 (neurotransmitter transporter, L-proline), member 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20210422	MGI			PMID:30177871
1332525	Slc6a7	solute carrier family 6 (neurotransmitter transporter, L-proline), member 7	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210520	MGI			
1332525	Slc6a7	solute carrier family 6 (neurotransmitter transporter, L-proline), member 7	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20210422	MGI			PMID:30177871
1332525	Slc6a7	solute carrier family 6 (neurotransmitter transporter, L-proline), member 7	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20210422	MGI			PMID:30177871
1332525	Slc6a7	solute carrier family 6 (neurotransmitter transporter, L-proline), member 7	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20220519	MGI			
1332525	Slc6a7	solute carrier family 6 (neurotransmitter transporter, L-proline), member 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1332525	Slc6a7	solute carrier family 6 (neurotransmitter transporter, L-proline), member 7	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:30177871
1332525	Slc6a7	solute carrier family 6 (neurotransmitter transporter, L-proline), member 7	gene	MP:0021088	impaired spatial memory extinction		IAGP		N	RGD:5509061	20220310	MGI			PMID:30177871
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20180308	MGI			PMID:29088697
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20180308	MGI			PMID:29088697
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20180308	MGI			PMID:29088697
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0005187	abnormal penis morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0005188	small penis		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0009104	small penile bone		IAGP		N	RGD:5509061	20221110	MGI			PMID:36196997
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0012474	decreased cingulate cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0012478	decreased secondary somatosensory cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0013909	small third ventricle		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:29088697
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:29088697
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29088697
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29088697
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20180308	MGI			PMID:29088697
1332528	Kctd13	potassium channel tetramerisation domain containing 13	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:29088697
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0002635	reduced sensorimotor gating		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18625319
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17690689
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0005604	hyperekplexia		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0012006	abnormal hippocampus physiology		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0014373	increased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0014620	abnormal interictal brain wave pattern		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332530	Arhgef9	CDC42 guanine nucleotide exchange factor 9	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:39374387
1332531	Slc22a17	solute carrier family 22 (organic cation transporter), member 17	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1332531	Slc22a17	solute carrier family 22 (organic cation transporter), member 17	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1332531	Slc22a17	solute carrier family 22 (organic cation transporter), member 17	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1332531	Slc22a17	solute carrier family 22 (organic cation transporter), member 17	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332533	Selenos	selenoprotein S	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20181220	MGI			PMID:29668323
1332533	Selenos	selenoprotein S	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20181220	MGI			PMID:29668323
1332533	Selenos	selenoprotein S	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
1332533	Selenos	selenoprotein S	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
1332533	Selenos	selenoprotein S	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
1332533	Selenos	selenoprotein S	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
1332533	Selenos	selenoprotein S	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
1332533	Selenos	selenoprotein S	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20181220	MGI			PMID:28592916
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20170105	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20160811	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0000690	absent spleen		IEA		N	RGD:5509061	20170105	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20170105	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0002282	abnormal trachea morphology		IEA		N	RGD:5509061	20170105	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0008024	absent lymph nodes		IEA		N	RGD:5509061	20170105	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332534	Fbxw9	F-box and WD-40 domain protein 9	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1332535	Adam32	a disintegrin and metallopeptidase domain 32	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1332535	Adam32	a disintegrin and metallopeptidase domain 32	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1332535	Adam32	a disintegrin and metallopeptidase domain 32	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1332535	Adam32	a disintegrin and metallopeptidase domain 32	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1332535	Adam32	a disintegrin and metallopeptidase domain 32	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1332539	U2surp	U2 snRNP-associated SURP domain containing	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1332539	U2surp	U2 snRNP-associated SURP domain containing	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1332539	U2surp	U2 snRNP-associated SURP domain containing	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1332539	U2surp	U2 snRNP-associated SURP domain containing	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1332539	U2surp	U2 snRNP-associated SURP domain containing	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1332539	U2surp	U2 snRNP-associated SURP domain containing	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20250508	MGI			
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20160922	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20160922	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160922	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20160922	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160922	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20160922	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20160922	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0030963	abnormal brain ependyma motile cilium location or orientation		IAGP		N	RGD:5509061	20190725	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0030964	decreased brain ependyma motile cilium length		IAGP		N	RGD:5509061	20190725	MGI			PMID:23906841
1332541	Jhy	junctional cadherin complex regulator	gene	MP:0030966	decreased brain ependyma motile cilium number		IAGP		N	RGD:5509061	20190725	MGI			PMID:23906841
1332542	Gtsf1	gametocyte specific factor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19735653
1332542	Gtsf1	gametocyte specific factor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19735653
1332542	Gtsf1	gametocyte specific factor 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19735653
1332542	Gtsf1	gametocyte specific factor 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19735653
1332542	Gtsf1	gametocyte specific factor 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19735653
1332542	Gtsf1	gametocyte specific factor 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:19735653
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0000738	impaired muscle contractility		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0000738	impaired muscle contractility		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059270
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001282	short vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002421	abnormal cell-mediated immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059270
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20240516	MGI			PMID:36803766
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0003358	abnormal hypaxial muscle morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20211021	MGI			
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20240516	MGI			PMID:36803766
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19843959
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0004867	decreased platelet calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18952890
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20240516	MGI			PMID:36803766
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059270
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18952890
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20240516	MGI			PMID:36803766
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059270
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059270
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0009257	dilated seminiferous tubule		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0009817	decreased leukotriene level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18059270
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0010183	abnormal CD4-positive helper T cell morphology		IAGP		N	RGD:5509061	20170921	MGI			PMID:28294127
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18952890
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591248
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0012322	decreased total tissue mass		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0014389	decreased skeletal muscle fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20260122	MGI			PMID:39420094
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0020280	increased creatine kinase level		IAGP		N	RGD:5509061	20251016	MGI			PMID:39594579
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0020355	abnormal Sertoli cell barrier morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332545	Orai1	ORAI calcium release-activated calcium modulator 1	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:26969191
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106865
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106865
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106865
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308544
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308544
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308544
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106865
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308544
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308544
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308544
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0009584	decreased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106865
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106865
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0011705	absent fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17476360
1332546	Pggt1b	protein geranylgeranyltransferase type I, beta subunit	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:20308544
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0010355	abnormal first pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21149574
1332547	Kat7	K(lysine) acetyltransferase 7	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:21149574
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21467224
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20210114	MGI			PMID:32439544
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22087241
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20210114	MGI			PMID:32439544
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018277
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210114	MGI			PMID:32439544
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191107	MGI			PMID:30346946
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20210114	MGI			PMID:32439544
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24280126
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775082
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002899	fatigue		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018277
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22087241
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21467224
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003916	decreased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:24280126
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17018277
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775082
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21467224
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0004955	increased thymus weight		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775082
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20210114	MGI			PMID:32439544
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24280126
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24280126
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24280126
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24280126
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122419
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775082
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20160929	MGI			PMID:27622213
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24280126
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16775082
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0006237	abnormal choroid vasculature morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0006238	abnormal choriocapillaris morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20160414	MGI			PMID:21467224
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0008834	abnormal melanosome transport		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22087241
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22087241
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22087241
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009305	decreased retroperitoneal fat pad weight		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009426	decreased soleus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122419
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009710	anhedonia		IAGP		N	RGD:5509061	20141204	MGI			PMID:25259918
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22087241
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:24280126
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15760270
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15454086
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628400
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20160929	MGI			PMID:27622213
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20191107	MGI			PMID:30346946
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17932564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0013307	increased adrenal gland weight		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0013894	abnormal behavioral response to amphetamine		IAGP		N	RGD:5509061	20160929	MGI			PMID:27622213
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0014143	decreased body fat mass		IEA		N	RGD:5509061	20170420	MGI			
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0014396	decreased fat cell mitochondrial DNA content		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0014398	abnormal fat cell mitochondrial morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39965564
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0020038	retina macular degeneration		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0020875	decreased nervous system dopamine level		IAGP		N	RGD:5509061	20210114	MGI			PMID:32439544
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200220	MGI			PMID:29925537
1332548	Ppargc1a	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15760270
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20230601	MGI			
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33077892
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20220519	MGI			PMID:33077892
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20220519	MGI			PMID:33077892
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20201022	MGI			
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20211021	MGI			
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20220519	MGI			PMID:33077892
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0012450	decreased primary motor cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0012453	decreased retrosplenial granular cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0012474	decreased cingulate cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332551	Tlcd3b	TLC domain containing 3B	gene	MP:0012476	decreased piriform cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20160317	MGI			PMID:25251060
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20160317	MGI			PMID:25251060
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20160317	MGI			PMID:25251060
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160317	MGI			PMID:25251060
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160317	MGI			PMID:25251060
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160317	MGI			PMID:25251060
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20160317	MGI			PMID:25251060
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20160317	MGI			PMID:25251060
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0020931	increased susceptibility to Adenoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:25251060
1332552	Klrc1	killer cell lectin-like receptor subfamily C, member 1	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:25251060
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20250717	MGI			PMID:32863207
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20250717	MGI			PMID:32863207
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20250717	MGI			PMID:32863207
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20250717	MGI			PMID:32863207
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20250717	MGI			PMID:32863207
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20250717	MGI			PMID:32863207
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0014433	increased cytokine level		IAGP		N	RGD:5509061	20250717	MGI			PMID:32863207
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0014435	increased interferon level		IAGP		N	RGD:5509061	20250717	MGI			PMID:32863207
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0014437	increased interleukin level		IAGP		N	RGD:5509061	20250717	MGI			PMID:32863207
1332556	Sike1	suppressor of IKBKE 1	gene	MP:0014870	increased liver malondialdehyde level		IAGP		N	RGD:5509061	20260212	MGI			PMID:32863207
1332557	Gtpbp8	GTP-binding protein 8 (putative)	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1332557	Gtpbp8	GTP-binding protein 8 (putative)	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20260402	MGI			
1332557	Gtpbp8	GTP-binding protein 8 (putative)	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1332559	Gpr151	G protein-coupled receptor 151	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20190606	MGI			PMID:30395363
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20250605	MGI			PMID:38197861
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20250605	MGI			PMID:38197861
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20250605	MGI			PMID:38197861
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20190606	MGI			PMID:30395363
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20250605	MGI			PMID:38197861
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0003198	calcified tendon		IAGP		N	RGD:5509061	20190606	MGI			PMID:30395363
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0003442	decreased circulating glycerol level		IEA		N	RGD:5509061	20201022	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20190606	MGI			PMID:30395363
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20250605	MGI			PMID:38197861
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20190606	MGI			PMID:30395363
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20190606	MGI			PMID:30395363
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20210128	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:38197861
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20250605	MGI			PMID:38197861
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:38197861
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0009877	exostosis		IAGP		N	RGD:5509061	20190606	MGI			PMID:30395363
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0010313	increased osteoma incidence		IAGP		N	RGD:5509061	20190606	MGI			PMID:30395363
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250605	MGI			PMID:38197861
1332560	Cibar1	CBY1 interacting BAR domain containing 1	gene	MP:0013304	osteophytes		IAGP		N	RGD:5509061	20190606	MGI			PMID:30395363
1332561	Gkn2	gastrokine 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1332561	Gkn2	gastrokine 2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20211021	MGI			
1332561	Gkn2	gastrokine 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0002544	brachydactyly		IEA		N	RGD:5509061	20210826	MGI			
1332561	Gkn2	gastrokine 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220519	MGI			
1332561	Gkn2	gastrokine 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1332561	Gkn2	gastrokine 2	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0005211	increased stomach mucosa thickness		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1332561	Gkn2	gastrokine 2	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1332561	Gkn2	gastrokine 2	gene	MP:0013567	gastric gland atrophy		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0013662	decreased myeloid cell number		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332561	Gkn2	gastrokine 2	gene	MP:0020186	abnormal susceptibility to bacterial infection		IAGP		N	RGD:5509061	20170608	MGI			PMID:26974160
1332562	Tbc1d23	TBC1 domain family, member 23	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22312129
1332562	Tbc1d23	TBC1 domain family, member 23	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22312129
1332562	Tbc1d23	TBC1 domain family, member 23	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22312129
1332562	Tbc1d23	TBC1 domain family, member 23	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22312129
1332565	Rps18	ribosomal protein S18	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784405
1332566	Enah	ENAH actin regulator	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0008129	absent brain internal capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0008221	abnormal hippocampal commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0009026	abnormal brain pia mater morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0009027	abnormal subarachnoid space morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069337
1332566	Enah	ENAH actin regulator	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0011724	ectopic cortical neuron		IAGP		N	RGD:5509061	20141003	MGI			PMID:17988629
1332566	Enah	ENAH actin regulator	gene	MP:0014697	abnormal fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:22908313
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22539352
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22539352
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22539352
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22539352
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22539352
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0004500	increased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22539352
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896338
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:22539352
1332567	Uimc1	ubiquitin interaction motif containing 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:22896338
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0001539	decreased caudal vertebrae number		IEA		N	RGD:5509061	20141003	MGI			
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0003345	decreased rib number		IEA		N	RGD:5509061	20160804	MGI			
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0004647	decreased lumbar vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0004648	decreased thoracic vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101742
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20160804	MGI			
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160804	MGI			
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20141003	MGI			
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101742
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101742
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21085614
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18704116
1332569	Dusp4	dual specificity phosphatase 4	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20141003	MGI			
1332570	Zfp414	zinc finger protein 414	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20221215	MGI			
1332570	Zfp414	zinc finger protein 414	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20221215	MGI			
1332570	Zfp414	zinc finger protein 414	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20221215	MGI			
1332570	Zfp414	zinc finger protein 414	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20221215	MGI			
1332570	Zfp414	zinc finger protein 414	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20221215	MGI			
1332571	Smg8	SMG8 nonsense mediated mRNA decay factor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22855819
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22855819
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22855819
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:22855819
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:24349437
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24349437
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16820008
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22855819
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16820008
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18320035
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:35169021
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22855819
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22855819
1332573	Gja10	gap junction protein, alpha 10	gene	MP:0008520	disorganized retina outer plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22855819
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19584095
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20210916	MGI			PMID:28630914
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0002713	abnormal glycogen catabolism		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20210916	MGI			PMID:28630914
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19584095
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20210916	MGI			PMID:28630914
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20210916	MGI			PMID:28630914
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20210916	MGI			PMID:28630914
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:19584095
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20210916	MGI			PMID:28630914
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0012655	increased catalase level		IAGP		N	RGD:5509061	20201217	MGI			PMID:31098411
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0014775	decreased skeletal muscle enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:31098411
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0031635	increased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:28630914
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0031736	ventricular bigeminy		IAGP		N	RGD:5509061	20260716	MGI			PMID:28630914
1332578	Obscn	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	gene	MP:0031737	ventricular trigeminy		IAGP		N	RGD:5509061	20260716	MGI			PMID:28630914
1332579	Cnppd1	cyclin Pas1/PHO80 domain containing 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1332579	Cnppd1	cyclin Pas1/PHO80 domain containing 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220519	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20220519	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23007167
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18923670
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18923670
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170216	MGI			PMID:26291320
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212115
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001356	increased aggression towards female mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212115
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212115
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001375	abnormal mating preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441904
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001385	pup cannibalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22419158
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23007167
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22419158
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20220519	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170216	MGI			PMID:26291320
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467366
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18923670
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212115
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23467366
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:18923670
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0003877	abnormal serotonergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18665319
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:18923670
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20220811	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0005238	increased brain size		IEA		N	RGD:5509061	20220519	MGI			
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0005322	abnormal serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15247473
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18923670
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0005655	increased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0006276	abnormal autonomic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0008845	abnormal paraventricular hypothalamic nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23007167
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0008847	abnormal suprachiasmatic nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23007167
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722968
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441904
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22419158
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20170216	MGI			PMID:26291320
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:18212115
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:18923670
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0011016	increased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20722968
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0011021	abnormal circadian regulation of heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0011022	abnormal circadian regulation of systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19520831
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23007167
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170216	MGI			PMID:26291320
1332580	Tph2	tryptophan hydroxylase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1332581	Septin9	septin 9	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824004
1332581	Septin9	septin 9	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824004
1332581	Septin9	septin 9	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0010836	decreased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0010839	decreased CD8-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23644740
1332581	Septin9	septin 9	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21824004
1357431	Cia27_m	collagen induced arthritis 27 (mouse)	qtl	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15529344
1357431	Cia27_m	collagen induced arthritis 27 (mouse)	qtl	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20111116	MGI			PMID:17082620
1357431	Cia27_m	collagen induced arthritis 27 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15529344
1357431	Cia27_m	collagen induced arthritis 27 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15529344
1357432	Hdlcl1_m	HDL cholesterol level 1 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15514201
1357432	Hdlcl1_m	HDL cholesterol level 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15514201
1357433	Dbts2_m	diabetes 2 (mouse)	qtl	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357433	Dbts2_m	diabetes 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357434	Obsty1_m	obesity 1 (mouse)	qtl	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357435	Epfq2_m	epididymal fat pad weight QTL 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357435	Epfq2_m	epididymal fat pad weight QTL 2 (mouse)	qtl	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357435	Epfq2_m	epididymal fat pad weight QTL 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357436	Splq1_m	spleen weight QTL 1 (mouse)	qtl	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357436	Splq1_m	spleen weight QTL 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357436	Splq1_m	spleen weight QTL 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357437	Epfq4_m	epididymal fat pad weight QTL 4 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357437	Epfq4_m	epididymal fat pad weight QTL 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357438	Pwatq1_m	percent water in carcass QTL 1 (mouse)	qtl	MP:0000683	decreased percent water in carcass		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357438	Pwatq1_m	percent water in carcass QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357438	Pwatq1_m	percent water in carcass QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15058381
1357439	Popoa_m	premature ovulation and primary oocyte arrest (mouse)	qtl	MP:0001928	abnormal ovulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15509702
1357439	Popoa_m	premature ovulation and primary oocyte arrest (mouse)	qtl	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15509702
1357439	Popoa_m	premature ovulation and primary oocyte arrest (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20240510	MGI		Created by mouse qtl pipeline	PMID:15509702
1357439	Popoa_m	premature ovulation and primary oocyte arrest (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15509702
1357440	Hrtpq1_m	heart weight percentage QTL 1 (mouse)	qtl	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357440	Hrtpq1_m	heart weight percentage QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15058381
1357440	Hrtpq1_m	heart weight percentage QTL 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357441	Epfq3_m	epididymal fat pad weight QTL 3 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357441	Epfq3_m	epididymal fat pad weight QTL 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357442	Dbts1_m	diabetes 1 (mouse)	qtl	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357442	Dbts1_m	diabetes 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357443	Lhyp_m	lung hyperpermeability (mouse)	qtl	MP:0002295	abnormal pulmonary circulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:10783135
1357443	Lhyp_m	lung hyperpermeability (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10783135
1357443	Lhyp_m	lung hyperpermeability (mouse)	qtl	MP:0005388	respiratory system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10783135
1357444	Hdl35_m	HDL level 35 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9077551
1357444	Hdl35_m	HDL level 35 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9077551
1357447	Heal13_m	wound healing/regeneration 13 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:15225218
1357447	Heal13_m	wound healing/regeneration 13 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15225218
1357448	Bdywt_m	body weight (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15514201
1357448	Bdywt_m	body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15514201
1357449	Hcs6_m	hepatocarcinogenesis susceptibility 6 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7829059
1357449	Hcs6_m	hepatocarcinogenesis susceptibility 6 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:7829059
1357449	Hcs6_m	hepatocarcinogenesis susceptibility 6 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:7829059
1357450	Szs7_m	seizure susceptibility 7 (mouse)	qtl	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20111116	MGI			PMID:11472065
1357450	Szs7_m	seizure susceptibility 7 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1357450	Szs7_m	seizure susceptibility 7 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11472065
1357452	Vtbt18_m	vertebral trabecular bone trait 18 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357452	Vtbt18_m	vertebral trabecular bone trait 18 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357453	Kidq4_m	kidney weight QTL 4 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357453	Kidq4_m	kidney weight QTL 4 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357454	Kidq1_m	kidney weight QTL 1 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357454	Kidq1_m	kidney weight QTL 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357455	Trmq4_m	T cell ratio modifier QTL 4 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1357455	Trmq4_m	T cell ratio modifier QTL 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357455	Trmq4_m	T cell ratio modifier QTL 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357456	Hdl37_m	HDL level 37 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:9077551
1357456	Hdl37_m	HDL level 37 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9077551
1357459	Nhdlq7_m	non-HDL QTL 7 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357459	Nhdlq7_m	non-HDL QTL 7 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357460	Vtbt4_m	vertebral trabecular bone trait 4 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357460	Vtbt4_m	vertebral trabecular bone trait 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357461	Idd2_m	insulin dependent diabetes susceptibility 2 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7552995
1357461	Idd2_m	insulin dependent diabetes susceptibility 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:2576007|PMID:7578887|PMID:7556956
1357461	Idd2_m	insulin dependent diabetes susceptibility 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:2576007|PMID:7578887|PMID:7556956
1357461	Idd2_m	insulin dependent diabetes susceptibility 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:2576007|PMID:7578887|PMID:7556956
1357461	Idd2_m	insulin dependent diabetes susceptibility 2 (mouse)	qtl	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:7578887
1357462	Hlbsb1_m	hepatic lipase activity in BSB 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15314098
1357462	Hlbsb1_m	hepatic lipase activity in BSB 1 (mouse)	qtl	MP:0011581	increased triglyceride lipase activity		IAGP		N	RGD:5509061	20120209	MGI			PMID:15314098
1357463	Vtbt14_m	vertebral trabecular bone trait 14 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357463	Vtbt14_m	vertebral trabecular bone trait 14 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357465	Vtbt6_m	vertebral trabecular bone trait 6 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357465	Vtbt6_m	vertebral trabecular bone trait 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357467	Arigg4_m	anti-RBC IgG antibodies 4 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357467	Arigg4_m	anti-RBC IgG antibodies 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357468	Rplag_m	reduced platelet aggregation (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14739220
1357468	Rplag_m	reduced platelet aggregation (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14739220
1357468	Rplag_m	reduced platelet aggregation (mouse)	qtl	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14739220
1357469	Kidq5_m	kidney weight QTL 5 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357469	Kidq5_m	kidney weight QTL 5 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357470	Obq16_m	obesity QTL 16 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357470	Obq16_m	obesity QTL 16 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357470	Obq16_m	obesity QTL 16 (mouse)	qtl	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357470	Obq16_m	obesity QTL 16 (mouse)	qtl	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357471	Arigg10_m	anti-RBC IgG antibodies 10 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357471	Arigg10_m	anti-RBC IgG antibodies 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357472	Lmblgq6_m	limb length QTL 6 (mouse)	qtl	MP:0004348	long femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1357472	Lmblgq6_m	limb length QTL 6 (mouse)	qtl	MP:0004350	long humerus		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1357472	Lmblgq6_m	limb length QTL 6 (mouse)	qtl	MP:0004357	long tibia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1357472	Lmblgq6_m	limb length QTL 6 (mouse)	qtl	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1357472	Lmblgq6_m	limb length QTL 6 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1357472	Lmblgq6_m	limb length QTL 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1357475	w3q13_m	weight 3 weeks QTL 13 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1357475	w3q13_m	weight 3 weeks QTL 13 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1357476	Mdmsc4_m	modifier of muscularity 4 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14504233
1357476	Mdmsc4_m	modifier of muscularity 4 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14504233
1357477	Lgdr2_m	liver Gapd decay rate 2 (mouse)	qtl	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15519297
1357477	Lgdr2_m	liver Gapd decay rate 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15519297
1357478	Kdnw1_m	kidney weight 1 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357478	Kdnw1_m	kidney weight 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357478	Kdnw1_m	kidney weight 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15561968
1357479	Splwt1_m	spleen weight 1 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357479	Splwt1_m	spleen weight 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15561968
1357479	Splwt1_m	spleen weight 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357479	Splwt1_m	spleen weight 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357480	Igf1sl4_m	IGF-1 serum levels 4 (mouse)	qtl	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11033447
1357480	Igf1sl4_m	IGF-1 serum levels 4 (mouse)	qtl	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20201002	MGI			PMID:11033447
1357480	Igf1sl4_m	IGF-1 serum levels 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357480	Igf1sl4_m	IGF-1 serum levels 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357481	Aaj2_m	anxiety in A/J 2 (mouse)	qtl	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15371360
1357481	Aaj2_m	anxiety in A/J 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15371360
1357482	Nhdlq4_m	non-HDL QTL 4 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357482	Nhdlq4_m	non-HDL QTL 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:17536020
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181537
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181537
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:17536020
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181537
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181537
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181537
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181537
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:17536020
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20111116	MGI			PMID:17536020
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:17536020
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181537
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181537
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181537
1357484	Bsbob_m	BSB obesity (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:17536020
1357485	Lgq4_m	late growth QTL 4 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1357485	Lgq4_m	late growth QTL 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1357486	Bmch2_m	bone mechanical trait 2 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:15312250
1357486	Bmch2_m	bone mechanical trait 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15312250
1357487	ecs_m	epistatic circling SWR/J (mouse)	qtl	MP:0001394	circling		IAGP		N	RGD:5509061	20111116	MGI			PMID:11932245
1357487	ecs_m	epistatic circling SWR/J (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	
1357487	ecs_m	epistatic circling SWR/J (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20170616	MGI		Created by mouse qtl pipeline	PMID:12297623
1357488	Splq3_m	spleen weight QTL 3 (mouse)	qtl	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357488	Splq3_m	spleen weight QTL 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357488	Splq3_m	spleen weight QTL 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357490	Hlbsb2_m	hepatic lipase activity in BSB 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15314098
1357490	Hlbsb2_m	hepatic lipase activity in BSB 2 (mouse)	qtl	MP:0011581	increased triglyceride lipase activity		IAGP		N	RGD:5509061	20120209	MGI			PMID:15314098
1357491	Fmgty3_m	femur geometry 3 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357491	Fmgty3_m	femur geometry 3 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357491	Fmgty3_m	femur geometry 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357492	Tgct5_m	testicular germ cell tumor 5 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12566386
1357492	Tgct5_m	testicular germ cell tumor 5 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12566386
1357492	Tgct5_m	testicular germ cell tumor 5 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12566386
1357492	Tgct5_m	testicular germ cell tumor 5 (mouse)	qtl	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12566386
1357493	Lgaq3_m	late growth adjusted QTL 3 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1357493	Lgaq3_m	late growth adjusted QTL 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1357494	Obsty2_m	obesity 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357494	Obsty2_m	obesity 2 (mouse)	qtl	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357495	Gpdc1_m	G protein deficiency-induced colitis 1 (mouse)	qtl	MP:0002816	colitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15633125
1357495	Gpdc1_m	G protein deficiency-induced colitis 1 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15633125
1357495	Gpdc1_m	G protein deficiency-induced colitis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15633125
1357496	Lptl2_m	LPS-induced pulmonary TNF-alpha locus 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15177550
1357496	Lptl2_m	LPS-induced pulmonary TNF-alpha locus 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15177550
1357496	Lptl2_m	LPS-induced pulmonary TNF-alpha locus 2 (mouse)	qtl	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15177550
1357497	Stzid2_m	streptozotocin induced diabetes susceptibility 2 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12879252
1357497	Stzid2_m	streptozotocin induced diabetes susceptibility 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12879252
1357498	Noan2_m	nitrous oxide antinociception 2 (mouse)	qtl	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20111116	MGI			PMID:14706786
1357498	Noan2_m	nitrous oxide antinociception 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14706786
1357498	Noan2_m	nitrous oxide antinociception 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14706786
1357499	Depmq1_m	dependence on morphine QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15457340
1357499	Depmq1_m	dependence on morphine QTL 1 (mouse)	qtl	MP:0009753	enhanced behavioral response to morphine		IAGP		N	RGD:5509061	20111116	MGI			PMID:15457340
1357500	Mdmsc6_m	modifier of muscularity 6 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14504233
1357500	Mdmsc6_m	modifier of muscularity 6 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14504233
1357502	Pnhdlc2_m	plasma non-HDL cholesterol 2 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12810823
1357502	Pnhdlc2_m	plasma non-HDL cholesterol 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12810823
1357503	Nhdlq5_m	non-HDL QTL 5 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357503	Nhdlq5_m	non-HDL QTL 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0001147	small testis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0001169	abnormal bulbourethral gland morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0001925	male infertility		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0002717	abnormal male preputial gland morphology		IAGP		N	RGD:5509061	20121214	MGI			PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357504	Mhstq1_m	male hybrid sterility QTL 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15389318
1357505	Vtbt1_m	vertebral trabecular bone trait 1 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357505	Vtbt1_m	vertebral trabecular bone trait 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357506	W10q6_m	weight 10 weeks QTL 6 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1357506	W10q6_m	weight 10 weeks QTL 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1357507	Synch2_m	synechia 2 (mouse)	qtl	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15161859
1357507	Synch2_m	synechia 2 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15161859
1357508	Sle14_m	systematic lupus erythematosus susceptibility 14 (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15034079
1357508	Sle14_m	systematic lupus erythematosus susceptibility 14 (mouse)	qtl	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15034079
1357508	Sle14_m	systematic lupus erythematosus susceptibility 14 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:15034079
1357508	Sle14_m	systematic lupus erythematosus susceptibility 14 (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15034079
1357510	Hdl40_m	HDL level 40 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9077551
1357510	Hdl40_m	HDL level 40 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9077551
1357511	Kidq3_m	kidney weight QTL 3 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357511	Kidq3_m	kidney weight QTL 3 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357512	Bsbob5_m	BSB obesity 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15166164
1357512	Bsbob5_m	BSB obesity 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15166164
1357512	Bsbob5_m	BSB obesity 5 (mouse)	qtl	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357512	Bsbob5_m	BSB obesity 5 (mouse)	qtl	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357513	Bwnd2wk2_m	body weight, NMR1 x DBA, 2 week, QTL 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15457339
1357513	Bwnd2wk2_m	body weight, NMR1 x DBA, 2 week, QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15457339
1357514	Mbis3_m	Mycobacterium bovis-induced systemic lupus erythematosus 3 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10903779
1357514	Mbis3_m	Mycobacterium bovis-induced systemic lupus erythematosus 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10903779
1357515	Lfq2_m	live fetuses QTL 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357515	Lfq2_m	live fetuses QTL 2 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357517	Bwtn1_m	body weight at necropsy 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357517	Bwtn1_m	body weight at necropsy 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357518	Tgyl1_m	triglyceride level 1 (mouse)	qtl	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357518	Tgyl1_m	triglyceride level 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357519	Vtbt12_m	vertebral trabecular bone trait 12 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357519	Vtbt12_m	vertebral trabecular bone trait 12 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357521	Bsbob4_m	BSB obesity 4 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357521	Bsbob4_m	BSB obesity 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15166164
1357521	Bsbob4_m	BSB obesity 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15166164
1357521	Bsbob4_m	BSB obesity 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15166164
1357521	Bsbob4_m	BSB obesity 4 (mouse)	qtl	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357522	Cia32_m	collagen induced arthritis 32 (mouse)	qtl	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1357522	Cia32_m	collagen induced arthritis 32 (mouse)	qtl	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15716976
1357522	Cia32_m	collagen induced arthritis 32 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357522	Cia32_m	collagen induced arthritis 32 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357523	Cia31_m	collagen induced arthritis 31 (mouse)	qtl	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1357523	Cia31_m	collagen induced arthritis 31 (mouse)	qtl	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15716976
1357523	Cia31_m	collagen induced arthritis 31 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357523	Cia31_m	collagen induced arthritis 31 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357524	W6q14_m	weight 6 weeks QTL 14 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1357524	W6q14_m	weight 6 weeks QTL 14 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1357525	Pnhdlc3_m	plasma non-HDL cholesterol 3 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12810823
1357525	Pnhdlc3_m	plasma non-HDL cholesterol 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12810823
1357526	Hyplip2_m	hyperlipidemia 2 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15331434
1357526	Hyplip2_m	hyperlipidemia 2 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15331434
1357526	Hyplip2_m	hyperlipidemia 2 (mouse)	qtl	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15331434
1357526	Hyplip2_m	hyperlipidemia 2 (mouse)	qtl	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20111116	MGI			PMID:15331434
1357526	Hyplip2_m	hyperlipidemia 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9974430
1357526	Hyplip2_m	hyperlipidemia 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9974430
1357527	Epfpq1_m	epididymal fat percentage QTL 1 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357527	Epfpq1_m	epididymal fat percentage QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357528	Nhdlq3_m	non-HDL QTL 3 (mouse)	qtl	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14872007
1357528	Nhdlq3_m	non-HDL QTL 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14872007
1357529	Lvrq8_m	liver weight QTL 8 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357529	Lvrq8_m	liver weight QTL 8 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357530	Bwnd2wk5_m	body weight, NMR1 x DBA, 2 week, QTL 5 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15457339
1357530	Bwnd2wk5_m	body weight, NMR1 x DBA, 2 week, QTL 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15457339
1357532	Bmch7_m	bone mechanical trait 7 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:15312250
1357532	Bmch7_m	bone mechanical trait 7 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15312250
1357533	Nwa2_m	New Zealand White autoimmunity 2 (mouse)	qtl	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:8805679
1357533	Nwa2_m	New Zealand White autoimmunity 2 (mouse)	qtl	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:8805679
1357533	Nwa2_m	New Zealand White autoimmunity 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8805679
1357534	Cinda3_m	cytokine induced activation 3 (mouse)	qtl	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15551356
1357534	Cinda3_m	cytokine induced activation 3 (mouse)	qtl	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15551356
1357534	Cinda3_m	cytokine induced activation 3 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15551356
1357534	Cinda3_m	cytokine induced activation 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15551356
1357534	Cinda3_m	cytokine induced activation 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15551356
1357535	Arigg2_m	anti-RBC IgG antibodies 2 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357535	Arigg2_m	anti-RBC IgG antibodies 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357536	Fmgty5_m	femur geometry 5 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357536	Fmgty5_m	femur geometry 5 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357536	Fmgty5_m	femur geometry 5 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357536	Fmgty5_m	femur geometry 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357537	Lith12_m	lithogenic gene 12 (mouse)	qtl	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12837957
1357537	Lith12_m	lithogenic gene 12 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151694
1357537	Lith12_m	lithogenic gene 12 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12837957|PMID:16151694
1357537	Lith12_m	lithogenic gene 12 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12837957|PMID:16151694
1357538	Espq4_m	embryo survival preimplantation QTL 4 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357538	Espq4_m	embryo survival preimplantation QTL 4 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357539	Bsbob3_m	BSB obesity 3 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357539	Bsbob3_m	BSB obesity 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15166164
1357540	Mp53d1_m	modifier of p53-deficiency 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12592396
1357540	Mp53d1_m	modifier of p53-deficiency 1 (mouse)	qtl	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12592396
1357541	Hdl34_m	HDL level 34 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9077551
1357541	Hdl34_m	HDL level 34 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9077551
1357543	Arigm5_m	anti-RBC IgM antibodies 5 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357543	Arigm5_m	anti-RBC IgM antibodies 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357543	Arigm5_m	anti-RBC IgM antibodies 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15373903
1357544	Vtbt10_m	vertebral trabecular bone trait 10 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357544	Vtbt10_m	vertebral trabecular bone trait 10 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357545	Bwnd4wk4_m	body weight, NMR1 x DBA, 4 week, QTL 4 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15457339
1357545	Bwnd4wk4_m	body weight, NMR1 x DBA, 4 week, QTL 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15457339
1357546	Vtbt3_m	vertebral trabecular bone trait 3 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357546	Vtbt3_m	vertebral trabecular bone trait 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357550	Alcdp1_m	alcohol dependency 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11919667
1357550	Alcdp1_m	alcohol dependency 1 (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11919667
1357551	Stzid_m	streptozotocin induced diabetes susceptibility (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12879252
1357551	Stzid_m	streptozotocin induced diabetes susceptibility (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15670764|PMID:12879252
1357551	Stzid_m	streptozotocin induced diabetes susceptibility (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15670764|PMID:12879252
1357551	Stzid_m	streptozotocin induced diabetes susceptibility (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:12879252
1357551	Stzid_m	streptozotocin induced diabetes susceptibility (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15670764|PMID:12879252
1357552	Aaj4_m	anxiety in A/J 4 (mouse)	qtl	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15371360
1357552	Aaj4_m	anxiety in A/J 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15371360
1357555	Tesq2_m	testis weight QTL 2 (mouse)	qtl	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357555	Tesq2_m	testis weight QTL 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357555	Tesq2_m	testis weight QTL 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357557	Etan1_m	ether anesthesia 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15549469
1357557	Etan1_m	ether anesthesia 1 (mouse)	qtl	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20111116	MGI			PMID:15549469
1357558	Bmch4_m	bone mechanical trait 4 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:15312250
1357558	Bmch4_m	bone mechanical trait 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15312250
1357559	Scfq2_m	subcutaneous fat pad weight QTL 2 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357559	Scfq2_m	subcutaneous fat pad weight QTL 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357561	Mbsyd_m	metabolic syndrome (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15514201
1357561	Mbsyd_m	metabolic syndrome (mouse)	qtl	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15514201
1357561	Mbsyd_m	metabolic syndrome (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15514201
1357561	Mbsyd_m	metabolic syndrome (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15514201
1357562	Hmdc_m	heterogeneity of muscle Gapd decay constants (mouse)	qtl	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15519297
1357562	Hmdc_m	heterogeneity of muscle Gapd decay constants (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15519297
1357563	Bmch6_m	bone mechanical trait 6 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:15312250
1357563	Bmch6_m	bone mechanical trait 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15312250
1357565	wrmod1_m	wobbler modifier 1 (mouse)	qtl	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20111116	MGI			PMID:11930176
1357565	wrmod1_m	wobbler modifier 1 (mouse)	qtl	MP:0002183	gliosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11930176
1357565	wrmod1_m	wobbler modifier 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11930176
1357565	wrmod1_m	wobbler modifier 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20250606	MGI		Created by mouse qtl pipeline	PMID:11930176
1357566	Lfq3_m	live fetuses QTL 3 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357566	Lfq3_m	live fetuses QTL 3 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357567	Nidd3k_m	Nidd3 on KK-A&lt;y&gt; (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12115031
1357567	Nidd3k_m	Nidd3 on KK-A&lt;y&gt; (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12115031
1357567	Nidd3k_m	Nidd3 on KK-A&lt;y&gt; (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12115031
1357567	Nidd3k_m	Nidd3 on KK-A&lt;y&gt; (mouse)	qtl	MP:0006353	increased glycosylated hemoglobin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12115031
1357569	Fmgty13_m	femur geometry 13 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357569	Fmgty13_m	femur geometry 13 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357569	Fmgty13_m	femur geometry 13 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357569	Fmgty13_m	femur geometry 13 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357570	Pltct1_m	platelet count 1 (mouse)	qtl	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20111116	MGI			PMID:15520881
1357570	Pltct1_m	platelet count 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15520881
1357571	Hrtq2_m	heart weight QTL 2 (mouse)	qtl	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357571	Hrtq2_m	heart weight QTL 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357573	Fmgty2_m	femur geometry 2 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357573	Fmgty2_m	femur geometry 2 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357573	Fmgty2_m	femur geometry 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357574	Hcif1_m	hepatocarcinogenesis in females 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8650181
1357574	Hcif1_m	hepatocarcinogenesis in females 1 (mouse)	qtl	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20111116	MGI			PMID:8650181
1357574	Hcif1_m	hepatocarcinogenesis in females 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:8650181
1357574	Hcif1_m	hepatocarcinogenesis in females 1 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8650181
1357575	Wt10q2_m	body weight, 10 weeks, QTL 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1357575	Wt10q2_m	body weight, 10 weeks, QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1357577	Trmq3_m	T cell ratio modifier QTL 3 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15529344
1357577	Trmq3_m	T cell ratio modifier QTL 3 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:17082620
1357577	Trmq3_m	T cell ratio modifier QTL 3 (mouse)	qtl	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15529344
1357577	Trmq3_m	T cell ratio modifier QTL 3 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15529344
1357577	Trmq3_m	T cell ratio modifier QTL 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15529344
1357577	Trmq3_m	T cell ratio modifier QTL 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15529344
1357578	Manln5_m	mandible length 5 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357578	Manln5_m	mandible length 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357578	Manln5_m	mandible length 5 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357578	Manln5_m	mandible length 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357579	Dmyaq3_m	darker modification of yellow agouti QTL 3 (mouse)	qtl	MP:0001186	pigmentation phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12859623
1357579	Dmyaq3_m	darker modification of yellow agouti QTL 3 (mouse)	qtl	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20111116	MGI			PMID:12859623
1357579	Dmyaq3_m	darker modification of yellow agouti QTL 3 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12859623
1357580	Pltct2_m	platelet count 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15520881
1357580	Pltct2_m	platelet count 2 (mouse)	qtl	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15520881
1357581	Manln6_m	mandible length 6 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357581	Manln6_m	mandible length 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357581	Manln6_m	mandible length 6 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357581	Manln6_m	mandible length 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357582	Splq9_m	spleen weight QTL 9 (mouse)	qtl	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357582	Splq9_m	spleen weight QTL 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357582	Splq9_m	spleen weight QTL 9 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357583	Sle18_m	systematic lupus erythematosus susceptibility 18 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15314659
1357583	Sle18_m	systematic lupus erythematosus susceptibility 18 (mouse)	qtl	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16943797
1357583	Sle18_m	systematic lupus erythematosus susceptibility 18 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:16943797
1357583	Sle18_m	systematic lupus erythematosus susceptibility 18 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16943797|PMID:15314659
1357583	Sle18_m	systematic lupus erythematosus susceptibility 18 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:15314659
1357584	Splq6_m	spleen weight QTL 6 (mouse)	qtl	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357584	Splq6_m	spleen weight QTL 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357584	Splq6_m	spleen weight QTL 6 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357585	Manln3_m	mandible length 3 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357585	Manln3_m	mandible length 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357585	Manln3_m	mandible length 3 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357585	Manln3_m	mandible length 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357586	Mdmsc3_m	modifier of muscularity 3 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14504233
1357586	Mdmsc3_m	modifier of muscularity 3 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14504233
1357588	Manln18_m	mandible length 18 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357588	Manln18_m	mandible length 18 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357588	Manln18_m	mandible length 18 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357588	Manln18_m	mandible length 18 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357589	Kdnw2_m	kidney weight 2 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357589	Kdnw2_m	kidney weight 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357589	Kdnw2_m	kidney weight 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15561968
1357590	Bwnd2wk7_m	body weight, NMR1 x DBA, 2 week, QTL 7 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15457339
1357590	Bwnd2wk7_m	body weight, NMR1 x DBA, 2 week, QTL 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15457339
1357591	Tesq1_m	testis weight QTL 1 (mouse)	qtl	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357591	Tesq1_m	testis weight QTL 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357591	Tesq1_m	testis weight QTL 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357594	Estoq3_m	embryo survival total QTL 3 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357594	Estoq3_m	embryo survival total QTL 3 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357595	Phrtq1_m	percent heart QTL 1 (mouse)	qtl	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1357595	Phrtq1_m	percent heart QTL 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1357596	Tgct3_m	testicular germ cell tumor 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12566386
1357596	Tgct3_m	testicular germ cell tumor 3 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12566386
1357596	Tgct3_m	testicular germ cell tumor 3 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12566386
1357596	Tgct3_m	testicular germ cell tumor 3 (mouse)	qtl	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12566386
1357597	Arigm7_m	anti-RBC IgM antibodies 7 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357597	Arigm7_m	anti-RBC IgM antibodies 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357597	Arigm7_m	anti-RBC IgM antibodies 7 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15373903
1357599	msrvh1_m	modifier of susceptibility to renal vascular hypertrophy/hyperplasia 1 (mouse)	qtl	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14718357
1357599	msrvh1_m	modifier of susceptibility to renal vascular hypertrophy/hyperplasia 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14718357
1357599	msrvh1_m	modifier of susceptibility to renal vascular hypertrophy/hyperplasia 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14718357
1357600	Obq17_m	obesity QTL 17 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357600	Obq17_m	obesity QTL 17 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357600	Obq17_m	obesity QTL 17 (mouse)	qtl	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357600	Obq17_m	obesity QTL 17 (mouse)	qtl	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357601	Manln9_m	mandible length 9 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357601	Manln9_m	mandible length 9 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357601	Manln9_m	mandible length 9 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357601	Manln9_m	mandible length 9 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357602	Vtbt2_m	vertebral trabecular bone trait 2 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357602	Vtbt2_m	vertebral trabecular bone trait 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357605	Mdmsc5_m	modifier of muscularity 5 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14504233
1357605	Mdmsc5_m	modifier of muscularity 5 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14504233
1357606	Lgdr1_m	liver Gapd decay rate 1 (mouse)	qtl	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15519297
1357606	Lgdr1_m	liver Gapd decay rate 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15519297
1357610	Vtbt8_m	vertebral trabecular bone trait 8 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357610	Vtbt8_m	vertebral trabecular bone trait 8 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357612	Epfpq2_m	epididymal fat percentage QTL 2 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357612	Epfpq2_m	epididymal fat percentage QTL 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357613	Bsbob2_m	BSB obesity 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357613	Bsbob2_m	BSB obesity 2 (mouse)	qtl	MP:0001781	abnormal white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357613	Bsbob2_m	BSB obesity 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15166164
1357613	Bsbob2_m	BSB obesity 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15166164
1357613	Bsbob2_m	BSB obesity 2 (mouse)	qtl	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15166164
1357614	Bmca_m	bile mucin accumulation (mouse)	qtl	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20111116	MGI			PMID:12395324
1357614	Bmca_m	bile mucin accumulation (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12395324
1357614	Bmca_m	bile mucin accumulation (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20251017	MGI		Created by mouse qtl pipeline	PMID:12395324
1357617	Mp53d3_m	modifier of p53-deficiency 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12592396
1357617	Mp53d3_m	modifier of p53-deficiency 3 (mouse)	qtl	MP:0004503	decreased incidence of tumors by ionizing radiation induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:12592396
1357617	Mp53d3_m	modifier of p53-deficiency 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20260102	MGI		Created by mouse qtl pipeline	PMID:12592396
1357617	Mp53d3_m	modifier of p53-deficiency 3 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12592396
1357617	Mp53d3_m	modifier of p53-deficiency 3 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12592396
1357618	Splq5_m	spleen weight QTL 5 (mouse)	qtl	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357618	Splq5_m	spleen weight QTL 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357618	Splq5_m	spleen weight QTL 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357619	Obsty5_m	obesity 5 (mouse)	qtl	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357619	Obsty5_m	obesity 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357619	Obsty5_m	obesity 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357619	Obsty5_m	obesity 5 (mouse)	qtl	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357619	Obsty5_m	obesity 5 (mouse)	qtl	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357619	Obsty5_m	obesity 5 (mouse)	qtl	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357620	Aaj1_m	anxiety in A/J 1 (mouse)	qtl	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15371360
1357620	Aaj1_m	anxiety in A/J 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15371360
1357621	Bmch3_m	bone mechanical trait 3 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:15312250
1357621	Bmch3_m	bone mechanical trait 3 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15312250
1357622	Espq3_m	embryo survival preimplantation QTL 3 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357622	Espq3_m	embryo survival preimplantation QTL 3 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357623	Fmgty10_m	femur geometry 10 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357623	Fmgty10_m	femur geometry 10 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357623	Fmgty10_m	femur geometry 10 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357624	Arigm6_m	anti-RBC IgM antibodies 6 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357624	Arigm6_m	anti-RBC IgM antibodies 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357624	Arigm6_m	anti-RBC IgM antibodies 6 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15373903
1357626	Arigg9_m	anti-RBC IgG antibodies 9 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357626	Arigg9_m	anti-RBC IgG antibodies 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357627	Tgq2_m	triglyceride QTL 2 (mouse)	qtl	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357627	Tgq2_m	triglyceride QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357628	Manln13_m	mandible length 13 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357628	Manln13_m	mandible length 13 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357628	Manln13_m	mandible length 13 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357628	Manln13_m	mandible length 13 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357630	Tgq1_m	triglyceride QTL 1 (mouse)	qtl	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357630	Tgq1_m	triglyceride QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357631	Motr1_m	modifier of tubby retinal degeneration 1 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12076089
1357631	Motr1_m	modifier of tubby retinal degeneration 1 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12076089
1357631	Motr1_m	modifier of tubby retinal degeneration 1 (mouse)	qtl	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12076089
1357631	Motr1_m	modifier of tubby retinal degeneration 1 (mouse)	qtl	MP:0006070	increased retina photoreceptor cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:12076089
1357632	Vtbt9_m	vertebral trabecular bone trait 9 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357632	Vtbt9_m	vertebral trabecular bone trait 9 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357634	Splq7_m	spleen weight QTL 7 (mouse)	qtl	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357634	Splq7_m	spleen weight QTL 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357634	Splq7_m	spleen weight QTL 7 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357635	Splq4_m	spleen weight QTL 4 (mouse)	qtl	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357635	Splq4_m	spleen weight QTL 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357635	Splq4_m	spleen weight QTL 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357636	Arigm4_m	anti-RBC IgM antibodies 4 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357636	Arigm4_m	anti-RBC IgM antibodies 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357636	Arigm4_m	anti-RBC IgM antibodies 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15373903
1357639	Obsty4_m	obesity 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357639	Obsty4_m	obesity 4 (mouse)	qtl	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357640	Orq2_m	ovulation rate QTL 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357640	Orq2_m	ovulation rate QTL 2 (mouse)	qtl	MP:0031411	increased ovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:15672592
1357641	Arigm1_m	anti-RBC IgM antibodies 1 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357641	Arigm1_m	anti-RBC IgM antibodies 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357641	Arigm1_m	anti-RBC IgM antibodies 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15373903
1357642	Dmyaq1_m	darker modification of yellow agouti QTL 1 (mouse)	qtl	MP:0001186	pigmentation phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12859623
1357642	Dmyaq1_m	darker modification of yellow agouti QTL 1 (mouse)	qtl	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20111116	MGI			PMID:12859623
1357642	Dmyaq1_m	darker modification of yellow agouti QTL 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12859623
1357645	Lvrq9_m	liver weight QTL 9 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357645	Lvrq9_m	liver weight QTL 9 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357647	Fmgty7_m	femur geometry 7 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357647	Fmgty7_m	femur geometry 7 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357647	Fmgty7_m	femur geometry 7 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357647	Fmgty7_m	femur geometry 7 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357648	Obq18_m	obesity QTL 18 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357648	Obq18_m	obesity QTL 18 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15210844
1357648	Obq18_m	obesity QTL 18 (mouse)	qtl	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357649	Cbm5_m	cerebellum weight 5 (mouse)	qtl	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11438585
1357649	Cbm5_m	cerebellum weight 5 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11438585
1357651	Lgq5_m	late growth QTL 5 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1357651	Lgq5_m	late growth QTL 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1357652	Xydsq_m	X/Y dissociation QTL (mouse)	qtl	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357652	Xydsq_m	X/Y dissociation QTL (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20240510	MGI		Created by mouse qtl pipeline	PMID:15389318
1357652	Xydsq_m	X/Y dissociation QTL (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15389318
1357653	Rthyd2_m	resistance to thymic deletion 2 (mouse)	qtl	MP:0005002	abnormal T cell clonal deletion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15589170
1357653	Rthyd2_m	resistance to thymic deletion 2 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357653	Rthyd2_m	resistance to thymic deletion 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357653	Rthyd2_m	resistance to thymic deletion 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357654	Manln14_m	mandible length 14 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357654	Manln14_m	mandible length 14 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357654	Manln14_m	mandible length 14 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357654	Manln14_m	mandible length 14 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357655	Capsq2_m	capsaicin sensitivity related QTL 2 (mouse)	qtl	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20111116	MGI			PMID:14499433
1357655	Capsq2_m	capsaicin sensitivity related QTL 2 (mouse)	qtl	MP:0005394	taste/olfaction phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14499433
1357656	Hrtq3_m	heart weight QTL 3 (mouse)	qtl	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357656	Hrtq3_m	heart weight QTL 3 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357657	Pymr_m	Plasmodium yoelli malaria resistance (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11862405
1357657	Pymr_m	Plasmodium yoelli malaria resistance (mouse)	qtl	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:11862405
1357657	Pymr_m	Plasmodium yoelli malaria resistance (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11862405
1357659	Epfpq4_m	epididymal fat percentage QTL 4 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14657254
1357659	Epfpq4_m	epididymal fat percentage QTL 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357661	Eae2b_m	susceptibility to experimental allergic encephalomyelitis 2b (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517969
1357661	Eae2b_m	susceptibility to experimental allergic encephalomyelitis 2b (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517969
1357661	Eae2b_m	susceptibility to experimental allergic encephalomyelitis 2b (mouse)	qtl	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517969
1357662	Lprq4_m	lipoprotein QTL 4 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:7560076
1357662	Lprq4_m	lipoprotein QTL 4 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:7560076
1357662	Lprq4_m	lipoprotein QTL 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18048852|PMID:7560076
1357662	Lprq4_m	lipoprotein QTL 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150612	MGI		Created by mouse qtl pipeline	PMID:7560076
1357663	Rthyd1_m	resistance to thymic deletion 1 (mouse)	qtl	MP:0005002	abnormal T cell clonal deletion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15589170
1357663	Rthyd1_m	resistance to thymic deletion 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357663	Rthyd1_m	resistance to thymic deletion 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357663	Rthyd1_m	resistance to thymic deletion 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357664	Nba3_m	New Zealand Black autoimmunity 3 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12215897
1357664	Nba3_m	New Zealand Black autoimmunity 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12215897
1357665	Hlq1_m	heat loss QTL 1 (mouse)	qtl	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:10353911
1357665	Hlq1_m	heat loss QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10353911
1357667	Heal12_m	wound healing/regeneration 12 (mouse)	qtl	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20111116	MGI			PMID:15225218
1357667	Heal12_m	wound healing/regeneration 12 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15225218
1357668	Espq1_m	embryo survival preimplantation QTL 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357668	Espq1_m	embryo survival preimplantation QTL 1 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357669	Lprq1_m	lipoprotein QTL 1 (mouse)	qtl	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9974430
1357669	Lprq1_m	lipoprotein QTL 1 (mouse)	qtl	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9974430
1357669	Lprq1_m	lipoprotein QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9974430
1357672	Marif1_m	macrophage-associated risk inflammatory factor 1 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15150098
1357672	Marif1_m	macrophage-associated risk inflammatory factor 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15150098
1357672	Marif1_m	macrophage-associated risk inflammatory factor 1 (mouse)	qtl	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15150098
1357672	Marif1_m	macrophage-associated risk inflammatory factor 1 (mouse)	qtl	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15150098
1357673	Arigg7_m	anti-RBC IgG antibodies 7 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357673	Arigg7_m	anti-RBC IgG antibodies 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357674	Eae27_m	experimental allergic encephalomyelitis susceptibility 27 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517969
1357674	Eae27_m	experimental allergic encephalomyelitis susceptibility 27 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517969
1357674	Eae27_m	experimental allergic encephalomyelitis susceptibility 27 (mouse)	qtl	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517969
1357675	Manln17_m	mandible length 17 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357675	Manln17_m	mandible length 17 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357675	Manln17_m	mandible length 17 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357675	Manln17_m	mandible length 17 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357676	Tilss1_m	TNF-induced lethal shock susceptibility 1 (mouse)	qtl	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20111116	MGI			PMID:17404289
1357676	Tilss1_m	TNF-induced lethal shock susceptibility 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12089334|PMID:17404289
1357679	Egrm1_m	early growth rate, maternal effect 1 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20150409	MGI			PMID:12242647
1357679	Egrm1_m	early growth rate, maternal effect 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12242647
1357680	Idd23_m	insulin dependent diabetes susceptibility 23 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561967
1357680	Idd23_m	insulin dependent diabetes susceptibility 23 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561967
1357681	Hrtq1_m	heart weight QTL 1 (mouse)	qtl	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357681	Hrtq1_m	heart weight QTL 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357682	Phdlc1_m	plasma HDL cholesterol 1 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12810823
1357682	Phdlc1_m	plasma HDL cholesterol 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12810823
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11033447
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11918215
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:15549416
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11918215
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11918215
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15549416
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0002139	abnormal hepatobiliary system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15549416
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0003109	short femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:11918215
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20160609	MGI			PMID:11033447
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20160609	MGI			PMID:15542029
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20201002	MGI			PMID:11918215
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20201002	MGI			PMID:15549416
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:11033447
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15549416
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11918215
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:15542029
1357683	Igf1sl1_m	IGF-1 serum levels 1 (mouse)	qtl	MP:0021190	decreased bone mineral density of lumbar vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:15542029
1357684	Bmch5_m	bone mechanical trait 5 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:15312250
1357684	Bmch5_m	bone mechanical trait 5 (mouse)	qtl	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:15312250
1357684	Bmch5_m	bone mechanical trait 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15312250
1357685	Skts13_m	skin tumor sucseptibility 13 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12881723
1357685	Skts13_m	skin tumor sucseptibility 13 (mouse)	qtl	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12881723
1357685	Skts13_m	skin tumor sucseptibility 13 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12881723
1357686	Lmblgq2_m	limb length QTL 2 (mouse)	qtl	MP:0004350	long humerus		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1357686	Lmblgq2_m	limb length QTL 2 (mouse)	qtl	MP:0004370	long ulna		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1357686	Lmblgq2_m	limb length QTL 2 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1357686	Lmblgq2_m	limb length QTL 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1357688	Mgdr1_m	muscle Gapd decay rate 1 (mouse)	qtl	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15519297
1357688	Mgdr1_m	muscle Gapd decay rate 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15519297
1357689	Mdmsc1_m	modifier of muscularity 1 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14504233
1357689	Mdmsc1_m	modifier of muscularity 1 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14504233
1357690	Vtbt19_m	vertebral trabecular bone trait 19 (mouse)	qtl	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357690	Vtbt19_m	vertebral trabecular bone trait 19 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357693	Tcsz1_m	tooth central size 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:11973311
1357693	Tcsz1_m	tooth central size 1 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11973311
1357693	Tcsz1_m	tooth central size 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20171006	MGI		Created by mouse qtl pipeline	PMID:11973311
1357693	Tcsz1_m	tooth central size 1 (mouse)	qtl	MP:0030091	macrodontia		IAGP		N	RGD:5509061	20171005	MGI			PMID:11973311
1357694	Fmgty1_m	femur geometry 1 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357694	Fmgty1_m	femur geometry 1 (mouse)	qtl	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357694	Fmgty1_m	femur geometry 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357694	Fmgty1_m	femur geometry 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357695	Pbrgcsf2_m	peripheral blood stem cell response to granulocyte colony stimulating factor 2 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14725902
1357695	Pbrgcsf2_m	peripheral blood stem cell response to granulocyte colony stimulating factor 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10688851
1357696	Cia30_m	collagen induced arthritis 30 (mouse)	qtl	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1357696	Cia30_m	collagen induced arthritis 30 (mouse)	qtl	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1357696	Cia30_m	collagen induced arthritis 30 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357696	Cia30_m	collagen induced arthritis 30 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357697	Carfhg2_m	carcass fat in high growth mice 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11309659
1357697	Carfhg2_m	carcass fat in high growth mice 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:11309659
1357697	Carfhg2_m	carcass fat in high growth mice 2 (mouse)	qtl	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:11309659
1357697	Carfhg2_m	carcass fat in high growth mice 2 (mouse)	qtl	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:16670015
1357698	Arigg6_m	anti-RBC IgG antibodies 6 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357698	Arigg6_m	anti-RBC IgG antibodies 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357699	Nhdlq6_m	non-HDL QTL 6 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357700	Thyct1_m	thymocyte count 1 (mouse)	qtl	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12944977
1357700	Thyct1_m	thymocyte count 1 (mouse)	qtl	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12944977
1357700	Thyct1_m	thymocyte count 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:12944977
1357700	Thyct1_m	thymocyte count 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12944977
1357700	Thyct1_m	thymocyte count 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12944977
1357701	Lvrq10_m	liver weight QTL 10 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357701	Lvrq10_m	liver weight QTL 10 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357702	Anth2_m	resistance to Bacillus anthracis 2 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:3143893
1357702	Anth2_m	resistance to Bacillus anthracis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:3143893
1357703	Vtbt17_m	vertebral trabecular bone trait 17 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357703	Vtbt17_m	vertebral trabecular bone trait 17 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357706	Lvrq2_m	liver weight QTL 2 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357706	Lvrq2_m	liver weight QTL 2 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357707	Elpfm_m	eye lens protein fluorescence emission (mouse)	qtl	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15519297
1357707	Elpfm_m	eye lens protein fluorescence emission (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15519297
1357708	Orq1_m	ovulation rate QTL 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357708	Orq1_m	ovulation rate QTL 1 (mouse)	qtl	MP:0031411	increased ovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:15672592
1357710	Arigm3_m	anti-RBC IgM antibodies 3 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357710	Arigm3_m	anti-RBC IgM antibodies 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357710	Arigm3_m	anti-RBC IgM antibodies 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15373903
1357711	Adbg1_m	adult body growth 1 (mouse)	qtl	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357711	Adbg1_m	adult body growth 1 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357711	Adbg1_m	adult body growth 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357711	Adbg1_m	adult body growth 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357713	Afpq9_m	abdominal fat percent QTL 9 (mouse)	qtl	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:11116089
1357713	Afpq9_m	abdominal fat percent QTL 9 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089
1357716	Bwnd5wk3_m	body weight, NMR1 x DBA, 5 week, QTL 3 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15457339
1357716	Bwnd5wk3_m	body weight, NMR1 x DBA, 5 week, QTL 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15457339
1357717	Hlpx_m	heterogeneity in eye lens protein photooxidation kinetics (mouse)	qtl	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15519297
1357717	Hlpx_m	heterogeneity in eye lens protein photooxidation kinetics (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15519297
1357719	Hipp3_m	hippocampal weight 3 (mouse)	qtl	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12953790
1357719	Hipp3_m	hippocampal weight 3 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12953790
1357720	Kidpq1_m	kidney weight percentage QTL 1 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357720	Kidpq1_m	kidney weight percentage QTL 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357720	Kidpq1_m	kidney weight percentage QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15058381
1357721	Sle17_m	systematic lupus erythematosus susceptibility 17 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15314659
1357721	Sle17_m	systematic lupus erythematosus susceptibility 17 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15314659
1357722	Vtbt11_m	vertebral trabecular bone trait 11 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357722	Vtbt11_m	vertebral trabecular bone trait 11 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357724	Fmgty6_m	femur geometry 6 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357724	Fmgty6_m	femur geometry 6 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357724	Fmgty6_m	femur geometry 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357725	Eae39_m	experimental allergic encephalomyelitis 39 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517969
1357725	Eae39_m	experimental allergic encephalomyelitis 39 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12517969
1357725	Eae39_m	experimental allergic encephalomyelitis 39 (mouse)	qtl	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12517969
1357726	Lnopy1_m	lens opacity 1 (mouse)	qtl	MP:0001304	cataract		IAGP		N	RGD:5509061	20111116	MGI			PMID:15161859
1357726	Lnopy1_m	lens opacity 1 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15161859
1357728	ecl1_m	epistatic circling C57L/J 1 (mouse)	qtl	MP:0001394	circling		IAGP		N	RGD:5509061	20111116	MGI			PMID:11932245
1357729	Marif2_m	macrophage-associated risk inflammatory factor 2 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15150098
1357729	Marif2_m	macrophage-associated risk inflammatory factor 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15150098
1357729	Marif2_m	macrophage-associated risk inflammatory factor 2 (mouse)	qtl	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15150098
1357729	Marif2_m	macrophage-associated risk inflammatory factor 2 (mouse)	qtl	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15150098
1357730	Hstx1_m	hybrid sterility, X chromosome 1 (mouse)	qtl	MP:0001925	male infertility		IAGP		N	RGD:5509061	20111116	MGI			PMID:15366371
1357730	Hstx1_m	hybrid sterility, X chromosome 1 (mouse)	qtl	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20111116	MGI			PMID:15366371
1357730	Hstx1_m	hybrid sterility, X chromosome 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15366371
1357730	Hstx1_m	hybrid sterility, X chromosome 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15366371
1357730	Hstx1_m	hybrid sterility, X chromosome 1 (mouse)	qtl	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20111116	MGI			PMID:15366371
1357731	Lvrq6_m	liver weight QTL 6 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357731	Lvrq6_m	liver weight QTL 6 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357734	Nba5_m	New Zealand Black autoimmunity 5 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15634937
1357734	Nba5_m	New Zealand Black autoimmunity 5 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15634937
1357734	Nba5_m	New Zealand Black autoimmunity 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15634937
1357734	Nba5_m	New Zealand Black autoimmunity 5 (mouse)	qtl	MP:0005615	increased susceptibility to type III hypersensitivity reaction		IAGP		N	RGD:5509061	20111116	MGI			PMID:15634937
1357735	Arigg3_m	anti-RBC IgG antibodies 3 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357735	Arigg3_m	anti-RBC IgG antibodies 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357737	Hpcr2_m	hepatocarcinogen resistance 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7705639
1357737	Hpcr2_m	hepatocarcinogen resistance 2 (mouse)	qtl	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:7705639
1357737	Hpcr2_m	hepatocarcinogen resistance 2 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:7705639
1357737	Hpcr2_m	hepatocarcinogen resistance 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7705639
1357737	Hpcr2_m	hepatocarcinogen resistance 2 (mouse)	qtl	MP:0010265	decreased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:7705639
1357738	Estoq2_m	embryo survival total QTL 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357738	Estoq2_m	embryo survival total QTL 2 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357739	Vtbt16_m	vertebral trabecular bone trait 16 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357739	Vtbt16_m	vertebral trabecular bone trait 16 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357740	Obsty3_m	obesity 3 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357740	Obsty3_m	obesity 3 (mouse)	qtl	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357740	Obsty3_m	obesity 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357740	Obsty3_m	obesity 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357740	Obsty3_m	obesity 3 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357740	Obsty3_m	obesity 3 (mouse)	qtl	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357740	Obsty3_m	obesity 3 (mouse)	qtl	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357740	Obsty3_m	obesity 3 (mouse)	qtl	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357740	Obsty3_m	obesity 3 (mouse)	qtl	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357741	Nidd5k_m	Nidd5 on KK-A&lt;y&gt; (mouse)	qtl	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12115031
1357741	Nidd5k_m	Nidd5 on KK-A&lt;y&gt; (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12115031
1357743	Lith3_m	lithogenic gene 3 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:12395324
1357743	Lith3_m	lithogenic gene 3 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12395324
1357744	Cfbw4_m	cystic fibrosis body weight 4 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12461646
1357744	Cfbw4_m	cystic fibrosis body weight 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12461646
1357745	Scfq4_m	subcutaneous fat pad weight QTL 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357745	Scfq4_m	subcutaneous fat pad weight QTL 4 (mouse)	qtl	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357745	Scfq4_m	subcutaneous fat pad weight QTL 4 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357746	Vtbt7_m	vertebral trabecular bone trait 7 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357746	Vtbt7_m	vertebral trabecular bone trait 7 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357747	Fob3a_m	F-line obesity QTL 3a (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181539
1357747	Fob3a_m	F-line obesity QTL 3a (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181539
1357747	Fob3a_m	F-line obesity QTL 3a (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181539
1357747	Fob3a_m	F-line obesity QTL 3a (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181539
1357749	Vtbt13_m	vertebral trabecular bone trait 13 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357749	Vtbt13_m	vertebral trabecular bone trait 13 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357750	Gpdc2_m	G protein deficiency-induced colitis 2 (mouse)	qtl	MP:0002816	colitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15633125
1357750	Gpdc2_m	G protein deficiency-induced colitis 2 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15633125
1357750	Gpdc2_m	G protein deficiency-induced colitis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15633125
1357751	ecl2_m	epistatic circling C57L/J 2 (mouse)	qtl	MP:0001394	circling		IAGP		N	RGD:5509061	20111116	MGI			PMID:11932245
1357752	Tabw_m	tally ho asscoiated body weight (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11414755
1357752	Tabw_m	tally ho asscoiated body weight (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11414755
1357753	Kidq2_m	kidney weight QTL 2 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357753	Kidq2_m	kidney weight QTL 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357754	Ahl3_m	age related hearing loss 3 (mouse)	qtl	MP:0004766	decreased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20111116	MGI			PMID:15504353
1357754	Ahl3_m	age related hearing loss 3 (mouse)	qtl	MP:0005377	hearing/vestibular/ear phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15504353
1357757	Lnopy2_m	lens opacity 2 (mouse)	qtl	MP:0001304	cataract		IAGP		N	RGD:5509061	20111116	MGI			PMID:15161859
1357757	Lnopy2_m	lens opacity 2 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15161859
1357758	Lptl1_m	LPS-induced pulmonary TNF-alpha locus 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15177550
1357758	Lptl1_m	LPS-induced pulmonary TNF-alpha locus 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15177550
1357758	Lptl1_m	LPS-induced pulmonary TNF-alpha locus 1 (mouse)	qtl	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15177550
1357759	W3q12_m	weight 3 weeks QTL 12 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1357759	W3q12_m	weight 3 weeks QTL 12 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1357760	Synch3_m	synechia 3 (mouse)	qtl	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15161859
1357760	Synch3_m	synechia 3 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15161859
1357761	Lfq1_m	live fetuses QTL 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357761	Lfq1_m	live fetuses QTL 1 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357762	Splq2_m	spleen weight QTL 2 (mouse)	qtl	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357762	Splq2_m	spleen weight QTL 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357762	Splq2_m	spleen weight QTL 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357764	Athla1_m	atherosclerotic lesion area 1 (mouse)	qtl	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20111116	MGI			PMID:15514201
1357764	Athla1_m	atherosclerotic lesion area 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15514201
1357765	Cmcs_m	cerebral malaria susceptibility in CBA/N (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15536567
1357765	Cmcs_m	cerebral malaria susceptibility in CBA/N (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15536567
1357767	Arigg5_m	anti-RBC IgG antibodies 5 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357767	Arigg5_m	anti-RBC IgG antibodies 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357768	Baa1_m	BALB/c autoimmunity 1 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:8805679
1357768	Baa1_m	BALB/c autoimmunity 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8805679
1357768	Baa1_m	BALB/c autoimmunity 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:8805679
1357772	Scfq1_m	subcutaneous fat pad weight QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357772	Scfq1_m	subcutaneous fat pad weight QTL 1 (mouse)	qtl	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357772	Scfq1_m	subcutaneous fat pad weight QTL 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357773	Espq2_m	embryo survival preimplantation QTL 2 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357773	Espq2_m	embryo survival preimplantation QTL 2 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357774	Fmgty8_m	femur geometry 8 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357774	Fmgty8_m	femur geometry 8 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357774	Fmgty8_m	femur geometry 8 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357775	Pbwg9_m	postnatal body weight growth 9 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15056934
1357775	Pbwg9_m	postnatal body weight growth 9 (mouse)	qtl	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20111116	MGI			PMID:16174331
1357779	Tesq3_m	testis weight QTL 3 (mouse)	qtl	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357779	Tesq3_m	testis weight QTL 3 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357779	Tesq3_m	testis weight QTL 3 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357784	Arti2_m	age related thymic involution 2 (mouse)	qtl	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20111116	MGI			PMID:12944977
1357784	Arti2_m	age related thymic involution 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:12944977
1357784	Arti2_m	age related thymic involution 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12944977
1357784	Arti2_m	age related thymic involution 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12944977
1357785	Cinda2_m	cytokine induced activation 2 (mouse)	qtl	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9177770
1357785	Cinda2_m	cytokine induced activation 2 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9177770
1357785	Cinda2_m	cytokine induced activation 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9177770
1357785	Cinda2_m	cytokine induced activation 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9177770
1357787	Vtbt5_m	vertebral trabecular bone trait 5 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357787	Vtbt5_m	vertebral trabecular bone trait 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357788	ecl_m	epistatic circling C57L/J (mouse)	qtl	MP:0001394	circling		IAGP		N	RGD:5509061	20111116	MGI			PMID:11932245
1357789	Kdnw3_m	kidney weight 3 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15561968
1357789	Kdnw3_m	kidney weight 3 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15561968
1357789	Kdnw3_m	kidney weight 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15561968
1357793	Pnhdlc1_m	plasma non-HDL cholesterol 1 (mouse)	qtl	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12810823
1357793	Pnhdlc1_m	plasma non-HDL cholesterol 1 (mouse)	qtl	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18048852
1357793	Pnhdlc1_m	plasma non-HDL cholesterol 1 (mouse)	qtl	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:18048852
1357793	Pnhdlc1_m	plasma non-HDL cholesterol 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:18048852|PMID:12810823
1357793	Pnhdlc1_m	plasma non-HDL cholesterol 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20150529	MGI		Created by mouse qtl pipeline	PMID:12810823
1357794	Cinda1_m	cytokine induced activation 1 (mouse)	qtl	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:9177770
1357794	Cinda1_m	cytokine induced activation 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9177770
1357794	Cinda1_m	cytokine induced activation 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9177770
1357794	Cinda1_m	cytokine induced activation 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9177770
1357795	Hdlcl2_m	HDL cholesterol level 2 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15514201
1357795	Hdlcl2_m	HDL cholesterol level 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15514201
1357796	Trmq5_m	T cell ratio modifier QTL 5 (mouse)	qtl	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15611280
1357796	Trmq5_m	T cell ratio modifier QTL 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357796	Trmq5_m	T cell ratio modifier QTL 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15611280
1357797	Splq8_m	spleen weight QTL 8 (mouse)	qtl	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357797	Splq8_m	spleen weight QTL 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357797	Splq8_m	spleen weight QTL 8 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357799	Igf1sl3_m	IGF-1 serum levels 3 (mouse)	qtl	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20201001	MGI			PMID:11033447
1357799	Igf1sl3_m	IGF-1 serum levels 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357800	Tgq3_m	triglyceride QTL 3 (mouse)	qtl	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357800	Tgq3_m	triglyceride QTL 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357801	Kidq7_m	kidney weight QTL 7 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357801	Kidq7_m	kidney weight QTL 7 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357802	Vtbt15_m	vertebral trabecular bone trait 15 (mouse)	qtl	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15005846
1357802	Vtbt15_m	vertebral trabecular bone trait 15 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15005846
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0001925	male infertility		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357804	Mhstq2_m	male hybrid sterility QTL 2 (mouse)	qtl	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20111116	MGI			PMID:15389318
1357806	Aaj3_m	anxiety in A/J 3 (mouse)	qtl	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15371360
1357806	Aaj3_m	anxiety in A/J 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15371360
1357807	Arigg1_m	anti-RBC IgG antibodies 1 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357807	Arigg1_m	anti-RBC IgG antibodies 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357808	Mgdr2_m	muscle Gapd decay rate 2 (mouse)	qtl	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15519297
1357808	Mgdr2_m	muscle Gapd decay rate 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15519297
1357811	Orq3_m	ovulation rate QTL 3 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357811	Orq3_m	ovulation rate QTL 3 (mouse)	qtl	MP:0031411	increased ovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:15672592
1357812	Kidq6_m	kidney weight QTL 6 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357812	Kidq6_m	kidney weight QTL 6 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357812	Kidq6_m	kidney weight QTL 6 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15058381
1357813	Ath20_m	atherosclerosis 20 (mouse)	qtl	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1357813	Ath20_m	atherosclerosis 20 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847
1357814	Hcs5_m	hepatocarcinogenesis susceptibility 5 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7829059
1357814	Hcs5_m	hepatocarcinogenesis susceptibility 5 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:7829059
1357814	Hcs5_m	hepatocarcinogenesis susceptibility 5 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:7829059
1357815	Fmgty4_m	femur geometry 4 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357815	Fmgty4_m	femur geometry 4 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357815	Fmgty4_m	femur geometry 4 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357816	Fmgty14_m	femur geometry 14 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357816	Fmgty14_m	femur geometry 14 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357816	Fmgty14_m	femur geometry 14 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357816	Fmgty14_m	femur geometry 14 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357817	Dmyaq2_m	darker modification of yellow agouti QTL 2 (mouse)	qtl	MP:0001186	pigmentation phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12859623
1357817	Dmyaq2_m	darker modification of yellow agouti QTL 2 (mouse)	qtl	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20111116	MGI			PMID:12859623
1357817	Dmyaq2_m	darker modification of yellow agouti QTL 2 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12859623
1357818	Grwtj1_m	growth trajectory 1 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15304622
1357818	Grwtj1_m	growth trajectory 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15304622
1357819	Tgct2_m	testicular germ cell tumor 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12566386
1357819	Tgct2_m	testicular germ cell tumor 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12566386
1357819	Tgct2_m	testicular germ cell tumor 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12566386
1357819	Tgct2_m	testicular germ cell tumor 2 (mouse)	qtl	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12566386
1357821	Arigg8_m	anti-RBC IgG antibodies 8 (mouse)	qtl	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357821	Arigg8_m	anti-RBC IgG antibodies 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357822	Lvrq3_m	liver weight QTL 3 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357822	Lvrq3_m	liver weight QTL 3 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357823	Spha3_m	sperm head anomaly 3 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15020476
1357823	Spha3_m	sperm head anomaly 3 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15020476
1357823	Spha3_m	sperm head anomaly 3 (mouse)	qtl	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15020476
1357824	Estoq4_m	embryo survival total QTL 4 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357824	Estoq4_m	embryo survival total QTL 4 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357825	Kidpq2_m	kidney weight percentage QTL 2 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357825	Kidpq2_m	kidney weight percentage QTL 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357826	Arti1_m	age related thymic involution 1 (mouse)	qtl	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20111116	MGI			PMID:12944977
1357826	Arti1_m	age related thymic involution 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:12944977
1357826	Arti1_m	age related thymic involution 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12944977
1357826	Arti1_m	age related thymic involution 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12944977
1357827	Hdl39_m	HDL level 39 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:9077551
1357827	Hdl39_m	HDL level 39 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9077551
1357828	Fmgty12_m	femur geometry 12 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357828	Fmgty12_m	femur geometry 12 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357828	Fmgty12_m	femur geometry 12 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357828	Fmgty12_m	femur geometry 12 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357829	Lvrq1_m	liver weight QTL 1 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357829	Lvrq1_m	liver weight QTL 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357831	Igf1sl2_m	IGF-1 serum levels 2 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:16675518
1357831	Igf1sl2_m	IGF-1 serum levels 2 (mouse)	qtl	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20201001	MGI			PMID:11033447
1357831	Igf1sl2_m	IGF-1 serum levels 2 (mouse)	qtl	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20111116	MGI			PMID:16675518
1357831	Igf1sl2_m	IGF-1 serum levels 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357831	Igf1sl2_m	IGF-1 serum levels 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357831	Igf1sl2_m	IGF-1 serum levels 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357831	Igf1sl2_m	IGF-1 serum levels 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11033447
1357831	Igf1sl2_m	IGF-1 serum levels 2 (mouse)	qtl	MP:0005568	increased circulating total protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11033447
1357831	Igf1sl2_m	IGF-1 serum levels 2 (mouse)	qtl	MP:0005568	increased circulating total protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16675518
1357835	Mp53d2_m	modifier of p53-deficiency 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12592396
1357835	Mp53d2_m	modifier of p53-deficiency 2 (mouse)	qtl	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12592396
1357837	Alcdp2_m	alcohol dependency 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11919667
1357837	Alcdp2_m	alcohol dependency 2 (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11919667
1357838	Noan1_m	nitrous oxide antinociception 1 (mouse)	qtl	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20111116	MGI			PMID:14706786
1357838	Noan1_m	nitrous oxide antinociception 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14706786
1357838	Noan1_m	nitrous oxide antinociception 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14706786
1357840	Lppl1_m	LPS-induced pulmonary PMN locus 1 (mouse)	qtl	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15177550
1357840	Lppl1_m	LPS-induced pulmonary PMN locus 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15177550
1357840	Lppl1_m	LPS-induced pulmonary PMN locus 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15177550
1357841	Phdlc2_m	plasma HDL cholesterol 2 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12810823
1357841	Phdlc2_m	plasma HDL cholesterol 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12810823
1357842	Hipp5_m	hippocampal weight 5 (mouse)	qtl	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12953790
1357842	Hipp5_m	hippocampal weight 5 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12953790
1357845	Rthyd3_m	resistance to thymic deletion 3 (mouse)	qtl	MP:0005002	abnormal T cell clonal deletion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15589170
1357845	Rthyd3_m	resistance to thymic deletion 3 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357845	Rthyd3_m	resistance to thymic deletion 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357845	Rthyd3_m	resistance to thymic deletion 3 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357849	Lbm8_m	lean body mass 8 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:12185457
1357849	Lbm8_m	lean body mass 8 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12185457
1357851	Scfq3_m	subcutaneous fat pad weight QTL 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357851	Scfq3_m	subcutaneous fat pad weight QTL 3 (mouse)	qtl	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357851	Scfq3_m	subcutaneous fat pad weight QTL 3 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357852	Manln8_m	mandible length 8 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357852	Manln8_m	mandible length 8 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357852	Manln8_m	mandible length 8 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357852	Manln8_m	mandible length 8 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357853	Dfq1_m	dead fetuses QTL 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357853	Dfq1_m	dead fetuses QTL 1 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20120727	MGI			PMID:21724994
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20120727	MGI			PMID:21724994
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20120727	MGI			PMID:21724994
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20120727	MGI			PMID:21724994
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20120727	MGI			PMID:21724994
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:17277141
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16943797
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16943797
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16943797
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:16943797
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:17277141
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:16943797
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20120727	MGI			PMID:21724994
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120720	MGI		Created by mouse qtl pipeline	PMID:16943797|PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120720	MGI		Created by mouse qtl pipeline	PMID:16943797|PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120720	MGI		Created by mouse qtl pipeline	PMID:16943797|PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16943797|PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120720	MGI		Created by mouse qtl pipeline	PMID:16943797|PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120720	MGI		Created by mouse qtl pipeline	PMID:16943797|PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120720	MGI		Created by mouse qtl pipeline	PMID:16943797|PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20160205	MGI		Created by mouse qtl pipeline	PMID:15314659
1357854	Sle16_m	systematic lupus erythematosus susceptibility 16 (mouse)	qtl	MP:0011508	abnormal glomerular capillary thrombosis		IAGP		N	RGD:5509061	20120727	MGI			PMID:21724994
1357855	Fob3b_m	F-line obesity QTL 3b (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151119	MGI			PMID:15181539
1357855	Fob3b_m	F-line obesity QTL 3b (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181539
1357855	Fob3b_m	F-line obesity QTL 3b (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181539
1357855	Fob3b_m	F-line obesity QTL 3b (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20151119	MGI			PMID:15181539
1357856	Baa2_m	BALB/c autoimmunity 2 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:8805679
1357856	Baa2_m	BALB/c autoimmunity 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8805679
1357856	Baa2_m	BALB/c autoimmunity 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:8805679
1357857	Lvrq5_m	liver weight QTL 5 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357857	Lvrq5_m	liver weight QTL 5 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357859	Lvrq7_m	liver weight QTL 7 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357859	Lvrq7_m	liver weight QTL 7 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357860	Aorls1_m	aortic lesion size 1 (mouse)	qtl	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20111116	MGI			PMID:12925895
1357860	Aorls1_m	aortic lesion size 1 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12925895
1357861	Bwnd4wk7_m	body weight, NMR1 x DBA, 4 week, QTL 7 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15457339
1357861	Bwnd4wk7_m	body weight, NMR1 x DBA, 4 week, QTL 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15457339
1357862	Epfq1_m	epididymal fat pad weight QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357862	Epfq1_m	epididymal fat pad weight QTL 1 (mouse)	qtl	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357862	Epfq1_m	epididymal fat pad weight QTL 1 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357863	Thyct2_m	thymocyte count 2 (mouse)	qtl	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12944977
1357863	Thyct2_m	thymocyte count 2 (mouse)	qtl	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20111116	MGI			PMID:12944977
1357863	Thyct2_m	thymocyte count 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20140627	MGI		Created by mouse qtl pipeline	PMID:12944977
1357863	Thyct2_m	thymocyte count 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12944977
1357863	Thyct2_m	thymocyte count 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12944977
1357864	Scfpq1_m	subcutaneous fat pad percentage QTL 1 (mouse)	qtl	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357864	Scfpq1_m	subcutaneous fat pad percentage QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357866	Bwnd3wk1_m	body weight, NMR1 x DBA, 3 week, QTL 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15457339
1357866	Bwnd3wk1_m	body weight, NMR1 x DBA, 3 week, QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15457339
1357868	Manln11_m	mandible length 11 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357868	Manln11_m	mandible length 11 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357868	Manln11_m	mandible length 11 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357868	Manln11_m	mandible length 11 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357869	Fmgty11_m	femur geometry 11 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357869	Fmgty11_m	femur geometry 11 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357869	Fmgty11_m	femur geometry 11 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357871	Bmch1_m	bone mechanical trait 1 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:15312250
1357871	Bmch1_m	bone mechanical trait 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15312250
1357872	Arigm2_m	anti-RBC IgM antibodies 2 (mouse)	qtl	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15373903
1357872	Arigm2_m	anti-RBC IgM antibodies 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15373903
1357872	Arigm2_m	anti-RBC IgM antibodies 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15373903
1357874	Manln1_m	mandible length 1 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1357874	Manln1_m	mandible length 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1357874	Manln1_m	mandible length 1 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357874	Manln1_m	mandible length 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1357876	Bdmsq_m	body mass QTL (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15339634
1357876	Bdmsq_m	body mass QTL (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15339634
1357877	Synch1_m	synechia 1 (mouse)	qtl	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15161859
1357877	Synch1_m	synechia 1 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15161859
1357878	Mastr_m	modifier of astrocytoma (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15319471
1357878	Mastr_m	modifier of astrocytoma (mouse)	qtl	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:15319471
1357878	Mastr_m	modifier of astrocytoma (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15319471
1357878	Mastr_m	modifier of astrocytoma (mouse)	qtl	MP:0010277	increased astrocytoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:15319471
1357879	Swrl1_m	SWR lupus locus 1 (mouse)	qtl	MP:0002532	abnormal type II hypersensitivity reaction		IAGP		N	RGD:5509061	20111116	MGI			PMID:11739537
1357879	Swrl1_m	SWR lupus locus 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12215897
1357879	Swrl1_m	SWR lupus locus 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20170505	MGI		Created by mouse qtl pipeline	PMID:11739537|PMID:12215897
1357879	Swrl1_m	SWR lupus locus 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:12215897
1357879	Swrl1_m	SWR lupus locus 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20170505	MGI		Created by mouse qtl pipeline	PMID:11739537|PMID:12215897
1357879	Swrl1_m	SWR lupus locus 1 (mouse)	qtl	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12215897
1357881	Estoq1_m	embryo survival total QTL 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672592
1357881	Estoq1_m	embryo survival total QTL 1 (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672592
1357882	Rthyd5_m	resistance to thymic deletion 5 (mouse)	qtl	MP:0005002	abnormal T cell clonal deletion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15589170
1357882	Rthyd5_m	resistance to thymic deletion 5 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357882	Rthyd5_m	resistance to thymic deletion 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357882	Rthyd5_m	resistance to thymic deletion 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15589170
1357883	Epfq5_m	epididymal fat pad weight QTL 5 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357883	Epfq5_m	epididymal fat pad weight QTL 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357885	Bwnd5wk7_m	body weight, NMR1 x DBA, 5 week, QTL 7 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15457339
1357885	Bwnd5wk7_m	body weight, NMR1 x DBA, 5 week, QTL 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15457339
1357886	Diht_m	dopamine-induced hypothermia (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15672594
1357886	Diht_m	dopamine-induced hypothermia (mouse)	qtl	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20111116	MGI			PMID:15672594
1357887	Cinda4_m	cytokine induced activation 4 (mouse)	qtl	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20111116	MGI			PMID:15551356
1357887	Cinda4_m	cytokine induced activation 4 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15551356
1357887	Cinda4_m	cytokine induced activation 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15551356
1357887	Cinda4_m	cytokine induced activation 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15551356
1357888	Aibl_m	adiposity index and body length (mouse)	qtl	MP:0001257	increased body length		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181538
1357888	Aibl_m	adiposity index and body length (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181538
1357889	Lprq3_m	lipoprotein QTL 3 (mouse)	qtl	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:7560076
1357889	Lprq3_m	lipoprotein QTL 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7560076
1357889	Lprq3_m	lipoprotein QTL 3 (mouse)	qtl	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:7560076
1357890	Hpcr1_m	hepatocarcinogen resistance 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7705639
1357890	Hpcr1_m	hepatocarcinogen resistance 1 (mouse)	qtl	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20111116	MGI			PMID:7705639
1357890	Hpcr1_m	hepatocarcinogen resistance 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:7705639
1357890	Hpcr1_m	hepatocarcinogen resistance 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7705639
1357890	Hpcr1_m	hepatocarcinogen resistance 1 (mouse)	qtl	MP:0010265	decreased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:7705639
1357891	Hcif2_m	hepatocarcinogenesis in females 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8650181
1357891	Hcif2_m	hepatocarcinogenesis in females 2 (mouse)	qtl	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20111116	MGI			PMID:8650181
1357891	Hcif2_m	hepatocarcinogenesis in females 2 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:8650181
1357891	Hcif2_m	hepatocarcinogenesis in females 2 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8650181
1357892	Marif3_m	macrophage-associated risk inflammatory factor 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15150098
1357892	Marif3_m	macrophage-associated risk inflammatory factor 3 (mouse)	qtl	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15150098
1357893	Lvrq4_m	liver weight QTL 4 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357893	Lvrq4_m	liver weight QTL 4 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357894	Epfpq3_m	epididymal fat percentage QTL 3 (mouse)	qtl	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058381
1357894	Epfpq3_m	epididymal fat percentage QTL 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058381
1357895	Ctrcts_m	cataract severity (mouse)	qtl	MP:0001304	cataract		IAGP		N	RGD:5509061	20111116	MGI			PMID:15161859
1357895	Ctrcts_m	cataract severity (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15161859
1357897	Lprq2_m	lipoprotein QTL 2 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9974430
1357897	Lprq2_m	lipoprotein QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9974430
1357898	Fmgty9_m	femur geometry 9 (mouse)	qtl	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357898	Fmgty9_m	femur geometry 9 (mouse)	qtl	MP:0001542	abnormal bone strength		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357898	Fmgty9_m	femur geometry 9 (mouse)	qtl	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20111116	MGI			PMID:12929939
1357898	Fmgty9_m	femur geometry 9 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357898	Fmgty9_m	femur geometry 9 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12929939
1357901	Mdmsc2_m	modifier of muscularity 2 (mouse)	qtl	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14504233
1357901	Mdmsc2_m	modifier of muscularity 2 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14504233
1357902	Obq19_m	obesity QTL 19 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15210844
1357902	Obq19_m	obesity QTL 19 (mouse)	qtl	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20111116	MGI			PMID:15210844
1357903	Gpdc3_m	G protein deficiency-induced colitis 3 (mouse)	qtl	MP:0002816	colitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15633125
1357903	Gpdc3_m	G protein deficiency-induced colitis 3 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15633125
1357903	Gpdc3_m	G protein deficiency-induced colitis 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15633125
1357904	Hdl36_m	HDL level 36 (mouse)	qtl	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20111116	MGI			PMID:9077551
1357904	Hdl36_m	HDL level 36 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9077551
13800899	Aap_m	active avoidance performance (mouse)	qtl	MP:0002798	abnormal active avoidance behavior		IAGP		N	RGD:5509061	20181025	MGI			PMID:1144596
13800899	Aap_m	active avoidance performance (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20181019	MGI		Created by mouse qtl pipeline	PMID:1144596
14700760	A830031A19Rik	RIKEN cDNA A830031A19 gene	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20201231	MGI			
15001487	Gm25679	predicted gene, 25679	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
15001487	Gm25679	predicted gene, 25679	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
15001487	Gm25679	predicted gene, 25679	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
15001487	Gm25679	predicted gene, 25679	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
15001487	Gm25679	predicted gene, 25679	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
15037099	Tel15q	telomeric sequence, Chr 15, q arm	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191128	MGI			PMID:23307865
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20191128	MGI			PMID:11106380
15037503	mt-Rnr2	16S rRNA, mitochondrial	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:11106380
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20240404	MGI			PMID:35998911
15037562	mt-Tl1	tRNA leucine 1, mitochondrial	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260716	MGI			PMID:35998911
15038098	mt-Tk	tRNA lysine, mitochondrial	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20191128	MGI			PMID:24510903
15038098	mt-Tk	tRNA lysine, mitochondrial	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20191128	MGI			PMID:24510903
15038098	mt-Tk	tRNA lysine, mitochondrial	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20191128	MGI			PMID:24510903
15038098	mt-Tk	tRNA lysine, mitochondrial	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20191128	MGI			PMID:24510903
15038209	mt-Tr	tRNA arginine, mitochondrial	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20191128	MGI			PMID:11175788
15038209	mt-Tr	tRNA arginine, mitochondrial	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20191128	MGI			PMID:11175788
15038209	mt-Tr	tRNA arginine, mitochondrial	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20191128	MGI			PMID:21803452
15038577	Tsil	thymus specific insertion locus	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191128	MGI			PMID:8786139
15038577	Tsil	thymus specific insertion locus	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20191128	MGI			PMID:8786139
15038577	Tsil	thymus specific insertion locus	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20191128	MGI			PMID:8786139
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0004600	abnormal vertebral transverse process morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0004606	absent vertebral spinous process		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0006253	clinodactyly		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0008829	triphalangia		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0008985	hemimelia		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0010772	abnormal pollex morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0010772	abnormal pollex morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0012528	abnormal zone of polarizing activity morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0030112	zygomatic bone hypoplasia		IAGP		N	RGD:5509061	20191128	MGI			PMID:23449628
15038936	Is(In8B2-8B3.1;6C1)1Tshir	Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1	gene	MP:0030835	abnormal ankle joint morphology		IAGP		N	RGD:5509061	20191128	MGI			PMID:7628698
15039113	mt-Ta	tRNA alanine, mitochondrial	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20191128	MGI			PMID:27626666
15039113	mt-Ta	tRNA alanine, mitochondrial	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20191128	MGI			PMID:27626666
15039113	mt-Ta	tRNA alanine, mitochondrial	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20191128	MGI			PMID:27626666
15039113	mt-Ta	tRNA alanine, mitochondrial	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20191128	MGI			PMID:27626666
15039113	mt-Ta	tRNA alanine, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20191128	MGI			PMID:27626666
15039113	mt-Ta	tRNA alanine, mitochondrial	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20191128	MGI			PMID:27626666
15039113	mt-Ta	tRNA alanine, mitochondrial	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20191128	MGI			PMID:27626666
15039113	mt-Ta	tRNA alanine, mitochondrial	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20191128	MGI			PMID:27626666
15039113	mt-Ta	tRNA alanine, mitochondrial	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:27626666
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:1442008
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:1927362
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001395	bidirectional circling		IEA		N	RGD:5509061	20111116	MGI			
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:1442008
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:1927362
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:1442008
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:1442008
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:1927362
1549969	Ush1g	USH1 protein network component sans	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20141003	MGI			PMID:1442008
1549969	Ush1g	USH1 protein network component sans	gene	MP:0003879	abnormal hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1927362
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004331	vestibular saccular macula degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:1927362
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1927362
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004405	absent cochlear hair cells		IEA		N	RGD:5509061	20111116	MGI			
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004413	absent cochlear microphonics		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004466	short cochlear outer hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1442008
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1442008
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004531	short outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004534	decreased inner hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004536	short inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004577	abnormal cochlear hair cell inter-stereocilial links morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004578	abnormal cochlear hair bundle tip links morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004813	absent linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1549969	Ush1g	USH1 protein network component sans	gene	MP:0004814	reduced linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1549969	Ush1g	USH1 protein network component sans	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:1927362
1549969	Ush1g	USH1 protein network component sans	gene	MP:0006335	abnormal hearing electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:1442008
1549969	Ush1g	USH1 protein network component sans	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:1927362
1549969	Ush1g	USH1 protein network component sans	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436032
1549969	Ush1g	USH1 protein network component sans	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22381527
1549969	Ush1g	USH1 protein network component sans	gene	MP:0030961	abnormal outer hair cell kinocilium location or orientation		IAGP		N	RGD:5509061	20190725	MGI			PMID:21436032
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20241121	MGI			
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497859
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:16950128
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:16950128
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20241121	MGI			
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497859
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497859
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16950128
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16950128
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16950128
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20976199
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497859
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:20976199
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497859
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16950128
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20200310	MGI			PMID:16950128
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497859
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497859
1549970	Actg1	actin, gamma, cytoplasmic 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:20976199
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0000336	decreased mast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20211021	MGI			
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0008091	decreased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0008697	decreased interleukin-3 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549973	Nfatc2ip	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133688
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0000228	abnormal thrombopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454133
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454133
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454133
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454133
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454133
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0003223	decreased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454133
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454133
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454133
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178777
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0011177	abnormal erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420462
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20160304	MGI			PMID:18048346
1549974	Bnip3l	BCL2/adenovirus E1B interacting protein 3-like	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:18454133
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0004520	short vestibular hair cell stereocilia		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0004523	decreased cochlear hair cell stereocilia number		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0004813	absent linear vestibular evoked potential		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0010015	abnormal cuticular plate morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549975	Capzb	capping actin protein of muscle Z-line subunit beta	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20171221	MGI			PMID:28899994
1549977	Fbxo28	F-box protein 28	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1549977	Fbxo28	F-box protein 28	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1549977	Fbxo28	F-box protein 28	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1549977	Fbxo28	F-box protein 28	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1549977	Fbxo28	F-box protein 28	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651901
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651901
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19651901
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1549978	Hmgn3	high mobility group nucleosomal binding domain 3	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141030	MGI			PMID:23620591
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210826	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210826	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220519	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210826	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210826	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20220811	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20210826	MGI			
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28530676
1549981	Dzip1l	DAZ interacting protein 1-like	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:28530676
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22130515
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21930766
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000288	abnormal pericardium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22926762
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24667635
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16510575
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20881014
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20200310	MGI			PMID:19738070
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10953035
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20200310	MGI			PMID:22666441
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000906	abnormal trigeminal V mesencephalic nucleus morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:15218525
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:22412863
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000959	abnormal somatic sensory system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16906226
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16906226
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20187849
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16906226
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430185
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:12812988
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:1528024
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430185
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:1528024
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:3221240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20200310	MGI			PMID:15306694
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15798202
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15218525
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22723298
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:16461894
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:22723298
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17491588
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:23520048
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18821589
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16510575
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18037992
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19738070
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430185
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:15218525
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:22723298
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20200310	MGI			PMID:12812988
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15798202
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20200310	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:12812988
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:12812988
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12812988
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418413
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15218525
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20187849
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8790342
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16510575
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265883
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15306694
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15561996
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15870264
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:17056592
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:18395839
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:18755891
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:24167636
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20231102	MGI			PMID:24411735
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430185
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430185
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12944494
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20531296
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23446734
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15798202
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20200310	MGI			PMID:20187849
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002738	hyperresponsive to tactile stimuli		IAGP		N	RGD:5509061	20200310	MGI			PMID:20187849
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22926762
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20200310	MGI			PMID:22290436
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:3221240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12388794
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:15201433
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:10625648
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:12388794
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:20484117
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15798202
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20200310	MGI			
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430185
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20484117
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24061480
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002969	impaired social transmission of food preference		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20200310	MGI			PMID:15306694
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:22733797
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20200310	MGI			PMID:28683291
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003171	phenotypic reversion		IAGP		N	RGD:5509061	20200310	MGI			PMID:2912572
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003228	abnormal sinus venosus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22926762
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11297820
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7509865
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:3221240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003350	increased circulating levels of thyroid hormone		IAGP		N	RGD:5509061	20200310	MGI			PMID:24265449
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:23770692
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22412863
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19458618
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:22733797
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:27895157
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:15306694
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:16510575
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21930766
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22733797
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15218525
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21930766
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22412863
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18037992
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22733797
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:20360310
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22412863
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16461894
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27895157
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20200310	MGI			PMID:12812988
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16461894
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004494	abnormal synaptic glutamate release		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430185
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24667635
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:22733797
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22290436
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18037992
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10953035
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12944494
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12944494
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005119	decreased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24265449
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16461894
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:27895157
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:18037992
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:24055366
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:27895157
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:22723298
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20484117
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24622775
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16906226
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20484117
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:9413985
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005468	abnormal thyroid hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24265449
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005470	increased thyroxine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24265449
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005477	increased circulating thyroxine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24265449
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23446734
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:21459331
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:27895157
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:15798202
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:27895157
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005583	decreased renin activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:15306694
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:15201433
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16461894
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:3221240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7509865
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24055366
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0006056	increased vascular endothelial cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15798202
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:18945948
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:21459331
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0006373	abnormal circulating angiotensinogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18945948
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20484117
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20200310	MGI			PMID:20484117
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20200310	MGI			PMID:20484117
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20200310	MGI			PMID:24061480
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23446734
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008301	adrenal medulla hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16906226
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430185
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430185
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18945948
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22290436
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:12944494
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:23770692
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24667635
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009179	abnormal pancreatic alpha cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19081794
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19081794
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12944494
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009436	fragmentation of sleep/wake states		IAGP		N	RGD:5509061	20200310	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20187849
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23770692
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010108	abnormal renal water reabsorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:21459331
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010160	increased oligodendrocyte number		IAGP		N	RGD:5509061	20201231	MGI			PMID:31932351
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:27895157
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19738070
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17018605
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28683291
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010449	heart right ventricle outflow tract stenosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:22926762
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010892	increased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20201231	MGI			PMID:31932351
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20200310	MGI			PMID:28683291
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20187849
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22926762
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17491588
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418413
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22412863
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20080592
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21930766
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22926762
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16906226
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15218525
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22412863
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22723298
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22723298
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011262	abnormal pharyngeal arch mesenchyme morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20200310	MGI			PMID:20484117
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22926762
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011426	abnormal ureter smooth muscle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20881014
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20484117
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20200310	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24055366
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20240118	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0012006	abnormal hippocampus physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28683291
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23770692
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:27297240
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19064922
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0012592	decreased brain choline acetyltransferase activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:7509865
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0012735	abnormal response to exercise		IAGP		N	RGD:5509061	20200310	MGI			PMID:28683291
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0014074	increased brain glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24452334
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0014234	decreased enterocyte apoptosis		IAGP		N	RGD:5509061	20230323	MGI			PMID:24667635
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0014365	impaired short-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:25100603
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0014813	abnormal brain glucose metabolism		IAGP		N	RGD:5509061	20251204	MGI			PMID:22096518
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0020078	decreased brain tyrosine 3-monooxygenase activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:7509865
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0020168	decreased thyroid gland weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24265449
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0020316	decreased vascular endothelial cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19458618
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:24452334
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0030971	ketoacidosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20364121
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0031232	increased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:18945948
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0031517	interrupted aortic arch, type c		IAGP		N	RGD:5509061	20240118	MGI			PMID:18058916
1549982	Hprt1	hypoxanthine phosphoribosyltransferase 1	gene	MP:0031590	abnormal epicardium development		IAGP		N	RGD:5509061	20240229	MGI			PMID:22926762
1549983	Gkn1	gastrokine 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20201231	MGI			
1549983	Gkn1	gastrokine 1	gene	MP:0000458	abnormal mandible morphology		IEA		N	RGD:5509061	20201231	MGI			
1549983	Gkn1	gastrokine 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1549983	Gkn1	gastrokine 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1549986	Zkscan17	zinc finger with KRAB and SCAN domains 17	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1549986	Zkscan17	zinc finger with KRAB and SCAN domains 17	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1549986	Zkscan17	zinc finger with KRAB and SCAN domains 17	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1549987	Wdr19	WD repeat domain 19	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000413	polyphalangy		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000568	ectopic digits		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0004420	parietal bone hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0004443	absent supraoccipital bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0011261	abnormal limb mesenchyme morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0011685	abnormal limb paddle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228095
1549987	Wdr19	WD repeat domain 19	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:22228095
1549988	Tlr9	toll-like receptor 9	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456769
1549988	Tlr9	toll-like receptor 9	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11130078
1549988	Tlr9	toll-like receptor 9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21683627
1549988	Tlr9	toll-like receptor 9	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11130078
1549988	Tlr9	toll-like receptor 9	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14563635
1549988	Tlr9	toll-like receptor 9	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11130078
1549988	Tlr9	toll-like receptor 9	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1549988	Tlr9	toll-like receptor 9	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118979
1549988	Tlr9	toll-like receptor 9	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11130078
1549988	Tlr9	toll-like receptor 9	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1549988	Tlr9	toll-like receptor 9	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21458307
1549988	Tlr9	toll-like receptor 9	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21683627
1549988	Tlr9	toll-like receptor 9	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16440059
1549988	Tlr9	toll-like receptor 9	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16703567
1549988	Tlr9	toll-like receptor 9	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456769
1549988	Tlr9	toll-like receptor 9	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135446
1549988	Tlr9	toll-like receptor 9	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389237
1549988	Tlr9	toll-like receptor 9	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0005093	decreased B cell proliferation		IEA		N	RGD:5509061	20111116	MGI			
1549988	Tlr9	toll-like receptor 9	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11130078
1549988	Tlr9	toll-like receptor 9	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1549988	Tlr9	toll-like receptor 9	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16703567
1549988	Tlr9	toll-like receptor 9	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20111116	MGI			
1549988	Tlr9	toll-like receptor 9	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456769
1549988	Tlr9	toll-like receptor 9	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389237
1549988	Tlr9	toll-like receptor 9	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389237
1549988	Tlr9	toll-like receptor 9	gene	MP:0008567	decreased interferon-gamma secretion		IEA		N	RGD:5509061	20111116	MGI			
1549988	Tlr9	toll-like receptor 9	gene	MP:0008573	increased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1549988	Tlr9	toll-like receptor 9	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389237
1549988	Tlr9	toll-like receptor 9	gene	MP:0008769	abnormal plasmacytoid dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1549988	Tlr9	toll-like receptor 9	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1549988	Tlr9	toll-like receptor 9	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:16818796
1549988	Tlr9	toll-like receptor 9	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:14993594
1549988	Tlr9	toll-like receptor 9	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:14993594
1549990	Chat	choline O-acetyltransferase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533614
1549990	Chat	choline O-acetyltransferase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:23374353
1549990	Chat	choline O-acetyltransferase	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879071
1549990	Chat	choline O-acetyltransferase	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20170223	MGI			PMID:26842965
1549990	Chat	choline O-acetyltransferase	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19421194
1549990	Chat	choline O-acetyltransferase	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879071
1549990	Chat	choline O-acetyltransferase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533614
1549990	Chat	choline O-acetyltransferase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879071
1549990	Chat	choline O-acetyltransferase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726636
1549990	Chat	choline O-acetyltransferase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:26842965
1549990	Chat	choline O-acetyltransferase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20230914	MGI			PMID:35767949
1549990	Chat	choline O-acetyltransferase	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1549990	Chat	choline O-acetyltransferase	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1549990	Chat	choline O-acetyltransferase	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1549990	Chat	choline O-acetyltransferase	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23374353
1549990	Chat	choline O-acetyltransferase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19116659
1549990	Chat	choline O-acetyltransferase	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533614
1549990	Chat	choline O-acetyltransferase	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23374353
1549990	Chat	choline O-acetyltransferase	gene	MP:0002337	abnormal whole-body plethysmography		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1549990	Chat	choline O-acetyltransferase	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20230914	MGI			PMID:35767949
1549990	Chat	choline O-acetyltransferase	gene	MP:0002913	abnormal PNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533614
1549990	Chat	choline O-acetyltransferase	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:24179230
1549990	Chat	choline O-acetyltransferase	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24179230
1549990	Chat	choline O-acetyltransferase	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0003928	increased heart rate variability		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0004085	abnormal heartbeat		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0005162	carpoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0005162	carpoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533614
1549990	Chat	choline O-acetyltransferase	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533614
1549990	Chat	choline O-acetyltransferase	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498043
1549990	Chat	choline O-acetyltransferase	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24179230
1549990	Chat	choline O-acetyltransferase	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879071
1549990	Chat	choline O-acetyltransferase	gene	MP:0005507	tail dragging		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1549990	Chat	choline O-acetyltransferase	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24179230
1549990	Chat	choline O-acetyltransferase	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20171221	MGI			PMID:28159985
1549990	Chat	choline O-acetyltransferase	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20230914	MGI			PMID:35767949
1549990	Chat	choline O-acetyltransferase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12879071
1549990	Chat	choline O-acetyltransferase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441053
1549990	Chat	choline O-acetyltransferase	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533614
1549990	Chat	choline O-acetyltransferase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230914	MGI			PMID:35767949
1549990	Chat	choline O-acetyltransferase	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20141016	MGI			PMID:24486622
1549990	Chat	choline O-acetyltransferase	gene	MP:0012593	increased brain choline acetyltransferase activity		IAGP		N	RGD:5509061	20170420	MGI			PMID:27810937
1549990	Chat	choline O-acetyltransferase	gene	MP:0015006	decreased fetal length		IAGP		N	RGD:5509061	20260611	MGI			PMID:12533614
1549990	Chat	choline O-acetyltransferase	gene	MP:0030676	increased acetylcholine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:27810937
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20180301	MGI			PMID:29097735
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0004115	abnormal sinoatrial node morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:29097735
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0004122	abnormal sinus arrhythmia		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20180301	MGI			PMID:29097735
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20180301	MGI			PMID:29097735
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0006142	abnormal sinoatrial node conduction		IAGP		N	RGD:5509061	20180301	MGI			PMID:29097735
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0010507	shortened RR interval		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0010511	shortened PR interval		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0010637	sinus bradycardia		IAGP		N	RGD:5509061	20180301	MGI			PMID:29097735
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0010999	proteinosis		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0011954	shortened PQ interval		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20180301	MGI			PMID:29097735
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20170907	MGI			PMID:27133129
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0020153	abnormal urine albumin level		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210520	MGI			
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0031003	increased kidney glycogen level		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20250515	MGI			PMID:27621313
1549995	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:27133129
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000376	folliculitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000414	alopecia		IEA		N	RGD:5509061	20200310	MGI			
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000765	abnormal tongue squamous epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0000997	abnormal synovial joint capsule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17538631
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:17538631
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002220	large lymphoid organs		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17538631
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20200310	MGI			PMID:17538631
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0003278	esophageal inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0003865	lymph node inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17538631
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0006162	thick eyelids		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20200618	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20200310	MGI			PMID:17538631
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0009715	thick epidermis stratum basale		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20200310	MGI			PMID:8774148
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0014349	absent spleen B cell follicles		IAGP		N	RGD:5509061	20240104	MGI			PMID:10201907
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0014349	absent spleen B cell follicles		IAGP		N	RGD:5509061	20240104	MGI			PMID:17538631
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0031395	cutaneous mastocytosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:8362989
1549996	Sharpin	SHANK-associated RH domain interacting protein	gene	MP:0031395	cutaneous mastocytosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:8774148
1549997	Prss3b	protease, serine 3B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230720	MGI			
1549997	Prss3b	protease, serine 3B	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230720	MGI			
1549997	Prss3b	protease, serine 3B	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20230720	MGI			
1549997	Prss3b	protease, serine 3B	gene	MP:0003340	acute pancreas inflammation		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0003341	chronic pancreas inflammation		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0008805	decreased circulating amylase level		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0009109	decreased pancreas weight		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230720	MGI			
1549997	Prss3b	protease, serine 3B	gene	MP:0009149	decreased pancreatic acinar cell number		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549997	Prss3b	protease, serine 3B	gene	MP:0013295	pancreas atrophy		IAGP		N	RGD:5509061	20190620	MGI			PMID:30487519
1549998	C1rl	complement component 1, r subcomponent-like	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20160421	MGI			
1549998	C1rl	complement component 1, r subcomponent-like	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20160421	MGI			
1549998	C1rl	complement component 1, r subcomponent-like	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1549998	C1rl	complement component 1, r subcomponent-like	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20201231	MGI			
1549999	Atp6v1e1	ATPase, H+ transporting, lysosomal V1 subunit E1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550001	Alpk1	alpha-kinase 1	gene	MP:0014495	increased circulating chemokine level		IAGP		N	RGD:5509061	20260219	MGI			PMID:35868845
1550001	Alpk1	alpha-kinase 1	gene	MP:0014902	increased circulating CCL2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:35868845
1550001	Alpk1	alpha-kinase 1	gene	MP:0031220	increased circulating CXCL10 level		IAGP		N	RGD:5509061	20240404	MGI			PMID:35868845
1550002	Prmt6	protein arginine N-methyltransferase 6	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:22904064
1550002	Prmt6	protein arginine N-methyltransferase 6	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22904064
1550002	Prmt6	protein arginine N-methyltransferase 6	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22904064
1550004	Spred3	sprouty-related EVH1 domain containing 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20200310	MGI			
1550004	Spred3	sprouty-related EVH1 domain containing 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20200310	MGI			
1550004	Spred3	sprouty-related EVH1 domain containing 3	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20200310	MGI			
1550004	Spred3	sprouty-related EVH1 domain containing 3	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20200310	MGI			
1550004	Spred3	sprouty-related EVH1 domain containing 3	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1550004	Spred3	sprouty-related EVH1 domain containing 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1550004	Spred3	sprouty-related EVH1 domain containing 3	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20220519	MGI			
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0011653	decreased circulating histidine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0012172	abnormal amniotic fluid composition		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0030668	decreased circulating proline level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0030674	decreased circulating alanine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550006	Slc43a2	solute carrier family 43, member 2	gene	MP:0030695	decreased circulating serine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25480797
1550007	Wipi2	WD repeat domain, phosphoinositide interacting 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1550007	Wipi2	WD repeat domain, phosphoinositide interacting 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550007	Wipi2	WD repeat domain, phosphoinositide interacting 2	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20241121	MGI			
1550008	Tinagl1	tubulointerstitial nephritis antigen-like 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:26522507
1550008	Tinagl1	tubulointerstitial nephritis antigen-like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:26522507
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20210506	MGI			PMID:33552067
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:24415953
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16571625
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691547
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12385751
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20231012	MGI			PMID:37334372
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20231012	MGI			PMID:37334372
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0003126	abnormal external female genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19282366
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0003553	abnormal foreskin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19282366
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0003936	abnormal reproductive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19282366
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0004711	persistence of notochord tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0005315	absent pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0006097	abnormal cerebellar lobule formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15496441
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18691547
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37334372
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20231012	MGI			PMID:37334372
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0009199	abnormal external male genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0009199	abnormal external male genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19282366
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0009569	abnormal left lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0009571	abnormal right lung accessory lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0009572	abnormal right lung cranial lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14723851
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20231012	MGI			PMID:37334372
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0011011	impaired lung lobe morphogenesis		IAGP		N	RGD:5509061	20200917	MGI			PMID:12361967
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12361967
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725236
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0021101	abnormal ventral interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:14723851
1550011	Gli1	GLI-Kruppel family member GLI1	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:14723851
1550015	Epdr1	ependymin related 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1550015	Epdr1	ependymin related 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20170105	MGI			
1550015	Epdr1	ependymin related 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1550015	Epdr1	ependymin related 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1550015	Epdr1	ependymin related 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1550016	Ust	uronyl-2-sulfotransferase	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1550016	Ust	uronyl-2-sulfotransferase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550017	Prkcb	protein kinase C, beta	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:10934237
1550017	Prkcb	protein kinase C, beta	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:10934237
1550017	Prkcb	protein kinase C, beta	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:23552399
1550017	Prkcb	protein kinase C, beta	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:8670417
1550017	Prkcb	protein kinase C, beta	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22761313
1550017	Prkcb	protein kinase C, beta	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23552399
1550017	Prkcb	protein kinase C, beta	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8670417
1550017	Prkcb	protein kinase C, beta	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:15662033
1550017	Prkcb	protein kinase C, beta	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8670417
1550017	Prkcb	protein kinase C, beta	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20200310	MGI			
1550017	Prkcb	protein kinase C, beta	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8670417
1550017	Prkcb	protein kinase C, beta	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23552399
1550017	Prkcb	protein kinase C, beta	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8670417
1550017	Prkcb	protein kinase C, beta	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1550017	Prkcb	protein kinase C, beta	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1550017	Prkcb	protein kinase C, beta	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23552399
1550017	Prkcb	protein kinase C, beta	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8670417
1550017	Prkcb	protein kinase C, beta	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23552399
1550017	Prkcb	protein kinase C, beta	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8670417
1550017	Prkcb	protein kinase C, beta	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20200310	MGI			
1550017	Prkcb	protein kinase C, beta	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20200310	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20241121	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27539859
1550019	Pi16	peptidase inhibitor 16	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27539859
1550019	Pi16	peptidase inhibitor 16	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0002344	abnormal lymph node B cell domain morphology		IEA		N	RGD:5509061	20200310	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0002359	abnormal spleen germinal center morphology		IEA		N	RGD:5509061	20200310	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0002397	abnormal bone marrow morphology		IEA		N	RGD:5509061	20200310	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20241121	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230119	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0004973	increased regulatory T cell number		IEA		N	RGD:5509061	20200310	MGI			
1550019	Pi16	peptidase inhibitor 16	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20231207	MGI			
1550021	Sucnr1	succinate receptor 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820681
1550021	Sucnr1	succinate receptor 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18535668
1550021	Sucnr1	succinate receptor 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820681
1550021	Sucnr1	succinate receptor 1	gene	MP:0003353	decreased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18535668
1550021	Sucnr1	succinate receptor 1	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820681
1550021	Sucnr1	succinate receptor 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820681
1550021	Sucnr1	succinate receptor 1	gene	MP:0005362	abnormal Langerhans cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820681
1550021	Sucnr1	succinate receptor 1	gene	MP:0008686	abnormal interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18820681
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20160623	MGI			PMID:26763459
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000678	abnormal parathyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391157
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391157
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689889
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001562	abnormal circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:11438569
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077299
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391157
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002249	abnormal larynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11826096
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482476
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689889
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689889
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002876	abnormal thyroid gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:11826096
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0002985	abnormal urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171764
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11826096
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0003996	clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689889
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0004697	abnormal thyroid follicular cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20161027	MGI			PMID:26168216
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005406	abnormal heart size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20160623	MGI			PMID:26763459
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12586747
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9296496
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20161027	MGI			PMID:26168216
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171764
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:9296496
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0009385	abnormal dermal pigmentation		IAGP		N	RGD:5509061	20160623	MGI			PMID:26763459
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0009387	abnormal epidermal pigmentation		IAGP		N	RGD:5509061	20160623	MGI			PMID:26763459
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774906
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0010326	malleus hypoplasia		IAGP		N	RGD:5509061	20170928	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0010640	ventricular myocardium compact layer hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689889
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9296496
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9391157
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689889
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077299
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20160623	MGI			PMID:26763459
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20160623	MGI			PMID:26763459
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0012045	increased susceptibility to hypertension		IAGP		N	RGD:5509061	20161027	MGI			PMID:26168216
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0020106	decreased nitrate level		IAGP		N	RGD:5509061	20161027	MGI			PMID:26168216
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:16988000
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0030107	incus hypoplasia		IAGP		N	RGD:5509061	20170928	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0030128	stapes hypoplasia		IAGP		N	RGD:5509061	20170928	MGI			PMID:9687499
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0030299	lower jaw to upper jaw transformation		IAGP		N	RGD:5509061	20171102	MGI			PMID:18199583
1550022	Gnaq	guanine nucleotide binding protein, alpha q polypeptide	gene	MP:0030884	rachitic rosary		IAGP		N	RGD:5509061	20181101	MGI			PMID:16988000
1550026	Popdc2	popeye domain containing 2	gene	MP:0004115	abnormal sinoatrial node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354168
1550026	Popdc2	popeye domain containing 2	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354168
1550026	Popdc2	popeye domain containing 2	gene	MP:0006142	abnormal sinoatrial node conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354168
1550026	Popdc2	popeye domain containing 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354168
1550026	Popdc2	popeye domain containing 2	gene	MP:0010637	sinus bradycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354168
1550027	Khdrbs3	KH domain containing, RNA binding, signal transduction associated 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1550027	Khdrbs3	KH domain containing, RNA binding, signal transduction associated 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637638
1550027	Khdrbs3	KH domain containing, RNA binding, signal transduction associated 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20231207	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0009453	enhanced contextual conditioning behavior		IEA		N	RGD:5509061	20231207	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0009455	enhanced cued conditioning behavior		IEA		N	RGD:5509061	20231207	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1550028	Ubqln4	ubiquilin 4	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0001785	edema		IEA		N	RGD:5509061	20260402	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20260402	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20260402	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20250508	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20230601	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0009931	abnormal skin appearance		IEA		N	RGD:5509061	20260402	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20230601	MGI			
1550029	Fbxo42	F-box protein 42	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1550033	Azin1	antizyme inhibitor 1	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19077035
1550033	Azin1	antizyme inhibitor 1	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19077035
1550033	Azin1	antizyme inhibitor 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19077035
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966563
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0000597	delayed hepatic development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121396
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20200116	MGI			PMID:27147662
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966563
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:27147662
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:27147662
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11121396
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0011877	absent liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200116	MGI			PMID:27147662
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:27147662
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:27147662
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0012235	abnormal liver bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550037	Icmt	isoprenylcysteine carboxyl methyltransferase	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12105862
1550042	Ppp2r5b	protein phosphatase 2, regulatory subunit B', beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20250424	MGI			PMID:35415460
1550043	Gjd4	gap junction protein, delta 4	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21272575
1550043	Gjd4	gap junction protein, delta 4	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21272575
1550043	Gjd4	gap junction protein, delta 4	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20201022	MGI			
1550043	Gjd4	gap junction protein, delta 4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1550043	Gjd4	gap junction protein, delta 4	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:21272575
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:11847113
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11847113
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11847113
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11847113
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11847113
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685933
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11847113
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0003794	delayed somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0004653	absent caudal vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11847113
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685933
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11847113
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550045	Tacc3	transforming, acidic coiled-coil containing protein 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359303
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210128	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20201022	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210128	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20201022	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240627	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20210128	MGI			
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550047	C1qtnf1	C1q and tumor necrosis factor related protein 1	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20170629	MGI			PMID:27555298
1550049	Pir	pirin	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1550050	Elavl3	ELAV like RNA binding protein 3	gene	MP:0000948	nonconvulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:22998874
1550050	Elavl3	ELAV like RNA binding protein 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22998874
1550050	Elavl3	ELAV like RNA binding protein 3	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22998874
1550050	Elavl3	ELAV like RNA binding protein 3	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:22998874
1550050	Elavl3	ELAV like RNA binding protein 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22998874
1550050	Elavl3	ELAV like RNA binding protein 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22998874
1550050	Elavl3	ELAV like RNA binding protein 3	gene	MP:0030737	decreased glutamic acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:22998874
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0008527	embryonic lethality at implantation		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20220519	MGI			
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1550052	Znhit2	zinc finger, HIT domain containing 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000264	failure of vascular branching		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000264	failure of vascular branching		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170209	MGI			
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000519	hydronephrosis		IEA		N	RGD:5509061	20170209	MGI			
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001619	abnormal vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003542	abnormal vascular endothelial cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0004056	abnormal myocardium compact layer morphology		IEA		N	RGD:5509061	20170209	MGI			
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0006344	small second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20170209	MGI			
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20170209	MGI			
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20170209	MGI			
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170209	MGI			
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093914
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15085193
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20170209	MGI			
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0012252	abnormal septum transversum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14675480
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221099
1550055	Mapk7	mitogen-activated protein kinase 7	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16710360
1550058	Adgra3	adhesion G protein-coupled receptor A3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:17882221
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20201022	MGI			
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18936251
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18936251
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18936251
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18936251
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18936251
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1550059	Stxbp5	syntaxin binding protein 5 (tomosyn)	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18936251
1550061	Calr	calreticulin	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085286
1550061	Calr	calreticulin	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085286
1550061	Calr	calreticulin	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0002952	ventricular cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085286
1550061	Calr	calreticulin	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085286
1550061	Calr	calreticulin	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085286
1550061	Calr	calreticulin	gene	MP:0004567	decreased myocardial fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0010498	abnormal interventricular septum muscular part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10085286
1550061	Calr	calreticulin	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0011701	decreased cumulus expansion		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0013283	failure of ventral body wall closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10739657
1550061	Calr	calreticulin	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0013891	increased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20160310	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:9126744
1550061	Calr	calreticulin	gene	MP:0014731	disorganized myocardial fiber myofibrils		IAGP		N	RGD:5509061	20250904	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0014737	decreased myocardial fiber myofibril thickness		IAGP		N	RGD:5509061	20250904	MGI			PMID:17112388
1550061	Calr	calreticulin	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0020463	increased megakaryocyte progenitor cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:29282219
1550061	Calr	calreticulin	gene	MP:0031018	decreased granulosa cell proliferation		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550061	Calr	calreticulin	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20240530	MGI			PMID:26388295
1550062	Ddah2	DDAH family member 2, ADMA independent	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550062	Ddah2	DDAH family member 2, ADMA independent	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101068
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230601	MGI			
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101068
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101068
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20230601	MGI			
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0004631	abnormal auditory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101068
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101068
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0014551	impaired neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:17218254
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0014557	increased cortical ventricular zone thickness		IAGP		N	RGD:5509061	20241031	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1550064	Tuba1a	tubulin, alpha 1A	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22101068
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21572435
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21572435
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0004478	increased testicular teratoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21572435
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21572435
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0009222	increased uterus tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550065	Cop1	COP1, E3 ubiquitin ligase	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21403399
1550066	Rfc1	replication factor C (activator 1) 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1550066	Rfc1	replication factor C (activator 1) 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1550066	Rfc1	replication factor C (activator 1) 1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20160811	MGI			
1550066	Rfc1	replication factor C (activator 1) 1	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20210826	MGI			
1550066	Rfc1	replication factor C (activator 1) 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1550066	Rfc1	replication factor C (activator 1) 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1550066	Rfc1	replication factor C (activator 1) 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1550066	Rfc1	replication factor C (activator 1) 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550066	Rfc1	replication factor C (activator 1) 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550067	Lrp12	low density lipoprotein-related protein 12	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20241121	MGI			
1550067	Lrp12	low density lipoprotein-related protein 12	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20230817	MGI			PMID:37330909
1550067	Lrp12	low density lipoprotein-related protein 12	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20230817	MGI			PMID:37330909
1550067	Lrp12	low density lipoprotein-related protein 12	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20230817	MGI			PMID:37330909
1550067	Lrp12	low density lipoprotein-related protein 12	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1550067	Lrp12	low density lipoprotein-related protein 12	gene	MP:0011804	increased cell migration		IAGP		N	RGD:5509061	20230817	MGI			PMID:37330909
1550067	Lrp12	low density lipoprotein-related protein 12	gene	MP:0020213	enhanced leukocyte migration		IAGP		N	RGD:5509061	20230817	MGI			PMID:37330909
1550068	Ddx17	DEAD box helicase 17	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20260402	MGI			
1550068	Ddx17	DEAD box helicase 17	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1550068	Ddx17	DEAD box helicase 17	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20260402	MGI			
1550068	Ddx17	DEAD box helicase 17	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1550068	Ddx17	DEAD box helicase 17	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1550068	Ddx17	DEAD box helicase 17	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1550070	Srsf6	serine and arginine-rich splicing factor 6	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1550070	Srsf6	serine and arginine-rich splicing factor 6	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1550070	Srsf6	serine and arginine-rich splicing factor 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1550071	Mtg2	mitochondrial ribosome associated GTPase 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1550071	Mtg2	mitochondrial ribosome associated GTPase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550071	Mtg2	mitochondrial ribosome associated GTPase 2	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1550071	Mtg2	mitochondrial ribosome associated GTPase 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550072	Tssk2	testis-specific serine kinase 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20240523	MGI			
1550076	Lars1	leucyl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1550077	Sil1	SIL1 nucleotide exchange factor	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116427
1550077	Sil1	SIL1 nucleotide exchange factor	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801575
1550077	Sil1	SIL1 nucleotide exchange factor	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116427
1550077	Sil1	SIL1 nucleotide exchange factor	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801575
1550077	Sil1	SIL1 nucleotide exchange factor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116427
1550077	Sil1	SIL1 nucleotide exchange factor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801575
1550077	Sil1	SIL1 nucleotide exchange factor	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:19801575
1550077	Sil1	SIL1 nucleotide exchange factor	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116427
1550078	Ankrd42	ankyrin repeat domain 42	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874121
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000033	absent scala media		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874121
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20221215	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20201022	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945933
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945933
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955062
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874121
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938278
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001512	trunk curl		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20201022	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945933
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002235	abnormal external nares morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22340499
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002659	pituitary gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002729	abnormal inner ear canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0002990	short ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003069	abnormal superior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003108	short zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003147	absent cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003164	decreased posterior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003166	decreased superior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938278
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210128	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003358	abnormal hypaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003358	abnormal hypaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003358	abnormal hypaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938278
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004161	cervical aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004248	abnormal epaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004248	abnormal epaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004313	absent vestibulocochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004314	absent inner ear vestibule		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004317	small vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004317	small vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004318	absent incus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004336	small utricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004396	decreased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004422	small temporal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004473	absent nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004666	absent stapedial artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874121
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004699	unilateral deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874121
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874121
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004873	absent turbinates		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004922	abnormal common crus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874121
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0005247	abnormal extraocular muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210520	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0005499	abnormal olfactory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006018	abnormal tympanic membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874121
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783782
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006211	small orbits		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006284	absent hypaxial muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006284	absent hypaxial muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006285	absent inner ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006286	inner ear hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19389353
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008023	abnormal styloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008064	decreased otic epithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008065	short endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628042
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008429	absent parotid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008430	short temporal bone squamous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16916509
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945933
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20241121	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0009520	decreased submandibular gland size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0009520	decreased submandibular gland size		IAGP		N	RGD:5509061	20150806	MGI			PMID:19371398
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0009913	abnormal hyoid bone greater horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0010466	vascular ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210520	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955062
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011366	absent metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011883	absent diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874121
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0013127	epistaxis		IAGP		N	RGD:5509061	20160407	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0013300	abnormal submandibular gland physiology		IAGP		N	RGD:5509061	20150806	MGI			PMID:19371398
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0013331	abnormal lacrimal gland development		IAGP		N	RGD:5509061	20141204	MGI			PMID:12834866
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0013541	abnormal submandibular gland development		IAGP		N	RGD:5509061	20150806	MGI			PMID:19371398
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0013595	absent vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0013929	absent eye muscles		IAGP		N	RGD:5509061	20171026	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0013964	absent tongue muscles		IAGP		N	RGD:5509061	20171026	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0014155	absent olfactory epithelium		IAGP		N	RGD:5509061	20160407	MGI			PMID:14695375
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0030208	abnormal intrinsic tongue muscle morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0030210	abnormal genioglossus muscle morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:12668636
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0030210	abnormal genioglossus muscle morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:15788460
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20171109	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0030421	tongue muscle hypoplasia		IAGP		N	RGD:5509061	20171214	MGI			PMID:21364285
1550080	Six1	sine oculis-related homeobox 1	gene	MP:0030426	facial muscle hypoplasia		IAGP		N	RGD:5509061	20171214	MGI			PMID:21364285
1550081	Mx2	MX dynamin-like GTPase 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200514	MGI			
1550081	Mx2	MX dynamin-like GTPase 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20201022	MGI			
1550081	Mx2	MX dynamin-like GTPase 2	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20211021	MGI			
1550081	Mx2	MX dynamin-like GTPase 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20200514	MGI			
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20181227	MGI			
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0000909	abnormal facial motor nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098279
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098279
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098279
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0001435	absent suckling reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098279
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20220519	MGI			
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098279
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098279
1550082	Clcf1	cardiotrophin-like cytokine factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170105	MGI			
1550083	Dusp7	dual specificity phosphatase 7	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1550083	Dusp7	dual specificity phosphatase 7	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1550083	Dusp7	dual specificity phosphatase 7	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1550083	Dusp7	dual specificity phosphatase 7	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1550083	Dusp7	dual specificity phosphatase 7	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170105	MGI			
1550083	Dusp7	dual specificity phosphatase 7	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20211021	MGI			
1550083	Dusp7	dual specificity phosphatase 7	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1550083	Dusp7	dual specificity phosphatase 7	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20211021	MGI			
1550083	Dusp7	dual specificity phosphatase 7	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230420	MGI			PMID:35596107
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956199
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956199
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956199
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956199
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956199
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20111116	MGI			
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956199
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956199
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956199
1550084	Gpr3	G-protein coupled receptor 3	gene	MP:0009007	short estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15956199
1550089	Mrm3	mitochondrial rRNA methyltransferase 3	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20200310	MGI			
1550089	Mrm3	mitochondrial rRNA methyltransferase 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20221215	MGI			
1550089	Mrm3	mitochondrial rRNA methyltransferase 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20200310	MGI			
1550089	Mrm3	mitochondrial rRNA methyltransferase 3	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1550089	Mrm3	mitochondrial rRNA methyltransferase 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550089	Mrm3	mitochondrial rRNA methyltransferase 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20200310	MGI			
1550089	Mrm3	mitochondrial rRNA methyltransferase 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1550089	Mrm3	mitochondrial rRNA methyltransferase 3	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240620	MGI			
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0013792	abnormal small intestine goblet cell morphology		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0013793	abnormal large intestine goblet cell morphology		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550090	Rprd1b	regulation of nuclear pre-mRNA domain containing 1B	gene	MP:0031319	impaired intestine regeneration		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:19356719
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19356719
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19356719
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19356719
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19356719
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19356719
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19356719
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19356719
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0011389	absent optic disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:19356719
1550091	Tfb1m	transcription factor B1, mitochondrial	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:19356719
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210520	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20200310	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29718959
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20200310	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:29718959
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:29718959
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:29718959
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200310	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20200310	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29718959
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29718959
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29718959
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:29718959
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20200310	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20230601	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0013510	decreased CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0013513	decreased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0013514	increased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1550092	Gimap6	GTPase, IMAP family member 6	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:29718959
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0000928	incomplete rostral neuropore closure		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0004180	failure of initiation of embryo turning		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0009657	failure of chorioallantoic fusion		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0012531	delayed limb development		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0013395	eyelid hypoplasia		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0014134	abnormal embryo morphology		IEA		N	RGD:5509061	20251204	MGI			
1550093	Gcn1	GCN1 activator of EIF2AK4	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20201022	MGI			PMID:32324833
1550095	Kcnk6	potassium inwardly-rectifying channel, subfamily K, member 6	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21876070
1550095	Kcnk6	potassium inwardly-rectifying channel, subfamily K, member 6	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21876070
1550095	Kcnk6	potassium inwardly-rectifying channel, subfamily K, member 6	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21876070
1550095	Kcnk6	potassium inwardly-rectifying channel, subfamily K, member 6	gene	MP:0004878	increased systemic vascular resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21876070
1550095	Kcnk6	potassium inwardly-rectifying channel, subfamily K, member 6	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21876070
1550095	Kcnk6	potassium inwardly-rectifying channel, subfamily K, member 6	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21876070
1550095	Kcnk6	potassium inwardly-rectifying channel, subfamily K, member 6	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21876070
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21584905
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20018883
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20111116	MGI			
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15334469
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800625
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21584905
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20018883
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IEA		N	RGD:5509061	20111116	MGI			
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20200514	MGI			
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21584905
1550099	Adamts4	ADAM metallopeptidase with thrombospondin type 1 motif 4	gene	MP:0011422	kidney medulla atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21584905
1550100	Scrn3	secernin 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20210617	MGI			PMID:25538260
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20210617	MGI			PMID:25538260
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:25538260
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20240523	MGI			
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210617	MGI			PMID:25538260
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20210617	MGI			PMID:25538260
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20210617	MGI			PMID:25538260
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160421	MGI			
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:25538260
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0020868	decreased lipogenesis		IAGP		N	RGD:5509061	20210617	MGI			PMID:25538260
1550101	Akr1b8	aldo-keto reductase family 1, member B8	gene	MP:0031319	impaired intestine regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:25538260
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849341
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849341
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849341
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849341
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849341
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849341
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849341
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1550103	Trafd1	TRAF type zinc finger domain containing 1	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18849341
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23243018
1550104	Cdcp1	CUB domain containing protein 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23243018
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550106	Yes1	YES proto-oncogene 1, Src family tyrosine kinase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958873
1550108	Dedd	death effector domain-containing	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283331
1550108	Dedd	death effector domain-containing	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283331
1550108	Dedd	death effector domain-containing	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283331
1550108	Dedd	death effector domain-containing	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283331
1550108	Dedd	death effector domain-containing	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283331
1550108	Dedd	death effector domain-containing	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283331
1550108	Dedd	death effector domain-containing	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283331
1550108	Dedd	death effector domain-containing	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17283331
1550110	Chp2	calcineurin-like EF hand protein 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1550110	Chp2	calcineurin-like EF hand protein 2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160421	MGI			
1550110	Chp2	calcineurin-like EF hand protein 2	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1550111	Dpyd	dihydropyrimidine dehydrogenase	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20181227	MGI			
1550111	Dpyd	dihydropyrimidine dehydrogenase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1550111	Dpyd	dihydropyrimidine dehydrogenase	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20181227	MGI			
1550111	Dpyd	dihydropyrimidine dehydrogenase	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20160811	MGI			
1550112	Fyttd1	forty-two-three domain containing 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1550112	Fyttd1	forty-two-three domain containing 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1550112	Fyttd1	forty-two-three domain containing 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230601	MGI			
1550112	Fyttd1	forty-two-three domain containing 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024804
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000080	abnormal exoccipital bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12183370
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12183370
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210805	MGI			
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210805	MGI			
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11520462
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210805	MGI			
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210805	MGI			
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15741318
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0003049	abnormal lumbar vertebrae morphology		IEA		N	RGD:5509061	20220811	MGI			
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024804
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004446	split exoccipital bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15741318
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15741318
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15741318
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024804
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004659	abnormal odontoid process morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004710	small notochord		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004713	split notochord		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11520462
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12183370
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024804
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11520462
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024804
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0006305	abnormal optic eminence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20200310	MGI			PMID:12183370
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15741318
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024804
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:15741318
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:8625838
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024804
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12183370
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21059868
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210805	MGI			
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0012180	abnormal somatic mesoderm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0012264	hindbrain hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550113	Pcgf2	polycomb group ring finger 2	gene	MP:0030834	acromion hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:11290297
1550115	Pudp	pseudouridine 5'-phosphatase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20200310	MGI			
1550115	Pudp	pseudouridine 5'-phosphatase	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1550115	Pudp	pseudouridine 5'-phosphatase	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220811	MGI			
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0012066	decreased astrocyte number		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0020389	increased radial glial cell number		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550116	Gatad2b	GATA zinc finger domain containing 2B	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20240222	MGI			PMID:38238293
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210128	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210826	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210128	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20220519	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210826	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20220811	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210826	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0008988	abnormal liver perisinusoidal space morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210826	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0011009	increased circulating glutamate dehydrogenase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31661432
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550118	Mfsd1	major facilitator superfamily domain containing 1	gene	MP:0031148	abnormal liver sinusoidal endothelial cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31661432
1550121	Hbb-y	hemoglobin Y, beta-like embryonic chain	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077320
1550122	Churc1	churchill domain containing 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1550122	Churc1	churchill domain containing 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1550122	Churc1	churchill domain containing 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1550122	Churc1	churchill domain containing 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210520	MGI			
1550122	Churc1	churchill domain containing 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210520	MGI			
1550122	Churc1	churchill domain containing 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1550122	Churc1	churchill domain containing 1	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20211021	MGI			
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16177061
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16177061
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16177061
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16177061
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378794
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934232
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16177061
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934232
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16177061
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16177061
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934232
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670336
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20656922
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934232
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16177061
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16177061
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16043658
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:16565390
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934232
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20656922
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10934232
1550123	Ltb4r1	leukotriene B4 receptor 1	gene	MP:0014706	decreased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:16670336
1550129	Sdhaf3	succinate dehydrogenase complex assembly factor 3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1550130	Erg	ETS transcription factor	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1550130	Erg	ETS transcription factor	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1550130	Erg	ETS transcription factor	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20190502	MGI			
1550130	Erg	ETS transcription factor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1550130	Erg	ETS transcription factor	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20190502	MGI			
1550130	Erg	ETS transcription factor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1550130	Erg	ETS transcription factor	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20171012	MGI			PMID:26097038
1550130	Erg	ETS transcription factor	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20171012	MGI			PMID:26097038
1550130	Erg	ETS transcription factor	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1550130	Erg	ETS transcription factor	gene	MP:0004125	abnormal venule morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1550130	Erg	ETS transcription factor	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0006137	venoocclusion		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:26097038
1550130	Erg	ETS transcription factor	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1550130	Erg	ETS transcription factor	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23512661
1550130	Erg	ETS transcription factor	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20201022	MGI			
1550130	Erg	ETS transcription factor	gene	MP:0010758	increased right ventricle systolic pressure		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18500345
1550130	Erg	ETS transcription factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22932696
1550130	Erg	ETS transcription factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20171012	MGI			PMID:26097038
1550130	Erg	ETS transcription factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550130	Erg	ETS transcription factor	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1550130	Erg	ETS transcription factor	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1550130	Erg	ETS transcription factor	gene	MP:0020161	increased vascular endothelial cell proliferation		IAGP		N	RGD:5509061	20160623	MGI			PMID:25062690
1550130	Erg	ETS transcription factor	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:18500345
1550133	Atp6ap1	ATPase, H+ transporting, lysosomal accessory protein 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20151112	MGI			PMID:22087256
1550133	Atp6ap1	ATPase, H+ transporting, lysosomal accessory protein 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20151112	MGI			PMID:22087256
1550133	Atp6ap1	ATPase, H+ transporting, lysosomal accessory protein 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22087256
1550133	Atp6ap1	ATPase, H+ transporting, lysosomal accessory protein 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20151112	MGI			PMID:22087256
1550133	Atp6ap1	ATPase, H+ transporting, lysosomal accessory protein 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11989824
1550133	Atp6ap1	ATPase, H+ transporting, lysosomal accessory protein 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20151112	MGI			PMID:22087256
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:24590285
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0000032	cochlear degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24333301
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9508777
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9508777
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:24333301
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24333301
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0003390	lymphedema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0003878	abnormal ear physiology		IAGP		N	RGD:5509061	20150226	MGI			PMID:24590285
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0003879	abnormal hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047635
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0003950	abnormal plasma membrane morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:24590285
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14686892
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14686892
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14686892
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:9508777
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24333301
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004465	degeneration of organ of Corti supporting cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004465	degeneration of organ of Corti supporting cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:24333301
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004482	abnormal interdental cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004562	abnormal inner hair cell synaptic ribbon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20150226	MGI			PMID:24590285
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0006403	abnormal cochlear endolymph ionic homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9508777
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0010194	absent lymphatic vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14686892
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9508777
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21807945
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0011521	decreased placental labyrinth size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9508777
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12121617
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20926451
1550135	Gjb2	gap junction protein, beta 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20150226	MGI			PMID:24590285
1550136	Cdhr1	cadherin-related family member 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11738025
1550136	Cdhr1	cadherin-related family member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672243
1550136	Cdhr1	cadherin-related family member 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11738025
1550136	Cdhr1	cadherin-related family member 1	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:11738025
1550139	Acvr2a	activin receptor IIA	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1550139	Acvr2a	activin receptor IIA	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000399	increased curvature of guard hairs		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000401	increased curvature of awl hairs		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000405	abnormal auchene hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20200310	MGI			
1550139	Acvr2a	activin receptor IIA	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20200310	MGI			PMID:16991118
1550139	Acvr2a	activin receptor IIA	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1550139	Acvr2a	activin receptor IIA	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1550139	Acvr2a	activin receptor IIA	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200310	MGI			
1550139	Acvr2a	activin receptor IIA	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16991118
1550139	Acvr2a	activin receptor IIA	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:16991118
1550139	Acvr2a	activin receptor IIA	gene	MP:0001749	suppressed circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16991118
1550139	Acvr2a	activin receptor IIA	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20221215	MGI			
1550139	Acvr2a	activin receptor IIA	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0003875	abnormal hair follicle regression		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20200310	MGI			PMID:16991118
1550139	Acvr2a	activin receptor IIA	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16991118
1550139	Acvr2a	activin receptor IIA	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:11416011
1550139	Acvr2a	activin receptor IIA	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11416011
1550139	Acvr2a	activin receptor IIA	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20221215	MGI			
1550139	Acvr2a	activin receptor IIA	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1550139	Acvr2a	activin receptor IIA	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0005072	abnormal hair follicle melanin granule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20250213	MGI			PMID:11416011
1550139	Acvr2a	activin receptor IIA	gene	MP:0006206	embryonic lethality between somite formation and embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16991118
1550139	Acvr2a	activin receptor IIA	gene	MP:0008732	reduced hair shaft melanin granule number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0008733	abnormal hair shaft melanin granule distribution		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0008767	abnormal hair medullary septa cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0008975	delayed male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0009002	premature hair regrowth		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0009351	thin hair shaft		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0009659	striated fur		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0010234	abnormal vibrissa follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0010389	mosaic coat color		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0010684	abnormal hair follicle outer root sheath morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:7885474
1550139	Acvr2a	activin receptor IIA	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550139	Acvr2a	activin receptor IIA	gene	MP:0011191	increased embryonic epiblast cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0012081	absent heart tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:16991118
1550139	Acvr2a	activin receptor IIA	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0012401	long nails		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452853
1550139	Acvr2a	activin receptor IIA	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:11416011
1550139	Acvr2a	activin receptor IIA	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:11416011
1550139	Acvr2a	activin receptor IIA	gene	MP:0030574	increased hair follicle cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0030918	small melanosome		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0030919	absent hair follicle bulb		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0030922	absent hair club		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0030924	early exit from telogen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0030925	early exit from anagen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611050
1550139	Acvr2a	activin receptor IIA	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:7885474
1550140	Parp3	poly (ADP-ribose) polymerase family, member 3	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21270334
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:22281501
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2090433
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2090433
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2090433
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22281501
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7894157
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2090433
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:2090433
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22281501
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0010653	abnormal Wallerian degeneration		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0012051	spasticity		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0014603	neuromuscular synapse degeneration		IAGP		N	RGD:5509061	20250206	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0020336	abnormal motor neuron dendrite morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0030191	narrow snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:22281501
1550141	Mdga2	MAM domain containing glycosylphosphatidylinositol anchor 2	gene	MP:0030835	abnormal ankle joint morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28040732
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0003060	increased aerobic running capacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550142	Slc25a25	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21296886
1550144	Meis2	Meis homeobox 2	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0001072	abnormal vestibulocochlear nerve morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0004383	absent interparietal bone		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0011615	submucous cleft palate		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0012250	absent heart valves		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0012747	abnormal cardiac neural crest cell morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0013183	absent trigeminal ganglion		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:26545946
1550144	Meis2	Meis homeobox 2	gene	MP:0013546	cleft soft palate		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:32169905
1550144	Meis2	Meis homeobox 2	gene	MP:0031458	absent palate bones		IAGP		N	RGD:5509061	20221124	MGI			PMID:32169905
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186026
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0000950	abnormal seizure response to pharmacological agent		IAGP		N	RGD:5509061	20151217	MGI			PMID:24452334
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186026
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186026
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20151217	MGI			PMID:24452334
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186026
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:25059425
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0002715	decreased glycogen catabolism rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21077101
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20151217	MGI			PMID:24452334
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186026
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0005440	increased glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538597
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186026
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20151217	MGI			PMID:24452334
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186026
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186026
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21077101
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20538597
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21077101
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20150723	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0014063	Lafora bodies		IAGP		N	RGD:5509061	20160304	MGI			PMID:20538597
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0014063	Lafora bodies		IAGP		N	RGD:5509061	20160304	MGI			PMID:21077101
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0014063	Lafora bodies		IAGP		N	RGD:5509061	20160304	MGI			PMID:21882344
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0014063	Lafora bodies		IAGP		N	RGD:5509061	20160304	MGI			PMID:22186026
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20160310	MGI			PMID:20538597
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0014074	increased brain glycogen level		IAGP		N	RGD:5509061	20160310	MGI			PMID:20538597
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0014074	increased brain glycogen level		IAGP		N	RGD:5509061	20190711	MGI			PMID:24452334
1550145	Nhlrc1	NHL repeat containing 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:24452334
1550146	Zbtb10	zinc finger and BTB domain containing 10	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1550146	Zbtb10	zinc finger and BTB domain containing 10	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1550147	Prokr2	prokineticin receptor 2	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220407	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202262
1550147	Prokr2	prokineticin receptor 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202262
1550147	Prokr2	prokineticin receptor 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0004894	uterus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0004895	vagina atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202262
1550147	Prokr2	prokineticin receptor 2	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202262
1550147	Prokr2	prokineticin receptor 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202262
1550147	Prokr2	prokineticin receptor 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1550147	Prokr2	prokineticin receptor 2	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:17202262
1550147	Prokr2	prokineticin receptor 2	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:17202262
1550148	Nt5dc1	5'-nucleotidase domain containing 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20200310	MGI			
1550148	Nt5dc1	5'-nucleotidase domain containing 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1550148	Nt5dc1	5'-nucleotidase domain containing 1	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1550148	Nt5dc1	5'-nucleotidase domain containing 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1550148	Nt5dc1	5'-nucleotidase domain containing 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550148	Nt5dc1	5'-nucleotidase domain containing 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20210722	MGI			PMID:11005611
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369263
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000397	abnormal guard hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369263
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000405	abnormal auchene hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369263
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567972
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369263
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000418	focal hair loss		IEA		N	RGD:5509061	20111116	MGI			
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000674	abnormal sweat gland morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:11005611
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567972
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369263
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567972
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:11005611
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20210722	MGI			PMID:11005611
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567972
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0002772	brachypodia		IAGP		N	RGD:5509061	20230824	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369263
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0003417	premature endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6682087
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0004703	abnormal vertebral column morphology		IEA		N	RGD:5509061	20111116	MGI			
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0004704	short vertebral column		IEA		N	RGD:5509061	20111116	MGI			
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369263
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0006253	clinodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0009938	abnormal hippocampus granule cell morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0010387	abnormal Bergmann glial cell morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369263
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14567972
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:4588955
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369263
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15639195
1550149	Nsdhl	NAD(P) dependent steroid dehydrogenase-like	gene	MP:0012204	abnormal neuronal stem cell physiology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25652406
1550152	Il12rb1	interleukin 12 receptor, beta 1	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18504307
1550152	Il12rb1	interleukin 12 receptor, beta 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1550152	Il12rb1	interleukin 12 receptor, beta 1	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9257825
1550152	Il12rb1	interleukin 12 receptor, beta 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9257825
1550152	Il12rb1	interleukin 12 receptor, beta 1	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9257825
1550152	Il12rb1	interleukin 12 receptor, beta 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1550152	Il12rb1	interleukin 12 receptor, beta 1	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20240523	MGI			
1550153	Cyth3	cytohesin 3	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0014476	abnormal feces lipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:30837656
1550153	Cyth3	cytohesin 3	gene	MP:0020868	decreased lipogenesis		IAGP		N	RGD:5509061	20191024	MGI			PMID:30837656
1550154	Rnf152	ring finger protein 152	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20240516	MGI			PMID:30514904
1550156	Ik	IK cytokine	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20240523	MGI			
1550156	Ik	IK cytokine	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1550156	Ik	IK cytokine	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1550156	Ik	IK cytokine	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550156	Ik	IK cytokine	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230601	MGI			
1550156	Ik	IK cytokine	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230601	MGI			
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20233966
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:30423293
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:15864294
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20200310	MGI			PMID:15864294
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16720837
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:15093544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000275	heart hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000316	cellular necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22892241
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23266956
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21514245
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000447	flattened snout		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21965329
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18372904
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15093544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20200310	MGI			PMID:22113502
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21965329
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:16720837
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371380
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000858	abnormal metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15093544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371380
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371380
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619626
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22350410
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281487
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17468755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:19151761
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20141835
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20697345
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25252692
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281487
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:22113502
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:22964582
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20200310	MGI			PMID:22113502
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:14681207
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619626
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:16288016
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:16585505
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:17349585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:17607363
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:17676035
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:17676052
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:18713982
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:19351816
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:21911454
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266220
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:22350410
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:23999427
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:25180607
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:28790031
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:18713982
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:25180607
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:28294115
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20240905	MGI			PMID:38733589
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20250605	MGI			PMID:31048544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001347	absent lacrimal glands		IAGP		N	RGD:5509061	20200310	MGI			PMID:22745308
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:22964582
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16720837
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20233966
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15093544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:16288213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281487
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22964582
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19629168
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20179099
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20230302	MGI			PMID:32552404
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19629168
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453624
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:21458673
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:22964582
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23999427
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14681207
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17468755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14706336
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114584
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20141835
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21458673
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24239359
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24591640
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27462406
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15837621
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16288016
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16288213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17468755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17676035
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281487
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18493606
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19151761
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19847165
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21317887
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21911454
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22430205
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611036
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22964582
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23285300
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23565506
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430184
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002030	increased neurofibrosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19846776
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17676052
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956606
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21512139
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24239359
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17607363
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20080688
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21965329
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20080688
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15837621
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16288016
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17468755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281487
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19061836
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21458673
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21911454
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22411819
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22606359
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22892241
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23285300
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24239348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430184
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:2891865
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:8152802
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17607363
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21504907
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22699621
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27462406
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27462406
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20220428	MGI			PMID:31400748
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20200310	MGI			PMID:17540175
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20200310	MGI			PMID:19847165
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20230302	MGI			PMID:32552404
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619626
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:16023597
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:16288016
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:16288213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17349585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17468755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17676035
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281487
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18372904
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18621715
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19151761
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19351816
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19846776
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20233966
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20697345
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21056012
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21317887
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368895
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21458673
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21504907
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21514245
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21911454
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21965329
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:22113502
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266220
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:22350410
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:22411819
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:22699621
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:22932805
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430184
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:27462406
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:28790031
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:28934293
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:30423293
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:31685994
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002138	abnormal hepatobiliary system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:14645534
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15864294
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:18059342
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371380
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18493606
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18493606
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19151761
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22411819
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:20233966
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19841240
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19841240
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002606	increased basophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16720837
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16720837
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002732	increased trichoepithelioma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23999427
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:15864294
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20697345
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18372904
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15864294
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20200310	MGI			PMID:29386660
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003277	increased esophageal papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003277	increased esophageal papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003335	exocrine pancreatic insufficiency		IAGP		N	RGD:5509061	20200310	MGI			PMID:21056012
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114584
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:19629168
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:23266956
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003390	lymphedema		IAGP		N	RGD:5509061	20200310	MGI			PMID:20179099
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19151761
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19847165
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23063435
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:26095252
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:27462406
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:31685994
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17607363
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19151761
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19847165
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20260611	MGI			PMID:39986371
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18372904
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003450	enlarged pancreas		IAGP		N	RGD:5509061	20200310	MGI			PMID:14706336
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21965329
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:26095252
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:15093544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19151761
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20697345
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22430205
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003750	increased mouth tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525739
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003752	increased oral papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003752	increased oral papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22699621
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003752	increased oral papilloma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525739
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003780	increased lip tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23266956
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21576358
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21576358
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20200310	MGI			PMID:16023597
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004155	decreased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17607363
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004230	abnormal embryonic erythrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15093544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004390	abnormal bronchoalveolar duct junction morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22411819
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:17607363
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:17607363
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15864294
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004839	bile duct hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29386660
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18372904
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004868	increased endometrial carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619626
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004882	enlarged lung		IAGP		N	RGD:5509061	20200310	MGI			PMID:17468755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20230302	MGI			PMID:32552404
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19841240
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21911454
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21911454
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005084	abnormal gallbladder morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16720837
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005119	decreased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19351816
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21458673
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:19629168
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:22113502
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005355	enlarged thyroid gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:19351816
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23597566
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281487
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266220
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005470	increased thyroxine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19351816
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005488	bronchial epithelial hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20200310	MGI			PMID:16720837
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006093	arteriovenous malformation		IAGP		N	RGD:5509061	20230302	MGI			PMID:32552404
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:15864294
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:15864294
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006321	increased myocardial fiber number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25813352
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20505730
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16288016
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17468755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17676035
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18264106
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281487
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19010921
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029981
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19061836
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19151761
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21317887
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21504907
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21512139
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22964582
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24276238
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27462406
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20210211	MGI			PMID:32767810
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008018	increased facial tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21911454
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:26095252
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19841240
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281487
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21514245
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611036
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22964582
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453624
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008717	increased lung squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17676035
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008718	increased lung large cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17676035
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:21514245
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008780	increased pancreatic acinar cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21056012
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20852630
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009043	increased pancreas adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22113502
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18713982
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009110	pancreas hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19629168
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009143	abnormal pancreatic duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009143	abnormal pancreatic duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25042889
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20200310	MGI			PMID:19629168
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29670173
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14681207
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14706336
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16585505
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114584
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17349585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18621715
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18713982
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21056012
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22611036
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22699621
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453624
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25042889
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25878147
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:28790031
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:28934293
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:31685994
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20260611	MGI			PMID:39986371
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14681207
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18713982
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19028870
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19028876
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19629168
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20473331
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22113502
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22699621
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25042889
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:26996122
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:28790031
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:28934293
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:29670173
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:31685994
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14681207
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16585505
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18713982
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19629168
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22113502
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22699621
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453624
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:26996122
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20241031	MGI			PMID:38574733
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009164	exocrine pancreas atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20200310	MGI			PMID:14681207
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009216	abnormal peritoneum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619626
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21965329
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21965329
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22350410
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009221	uterus adenomyosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19841240
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20200310	MGI			PMID:19629168
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16288016
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17676052
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20080688
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22113502
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22411819
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009320	increased lymphoblastic lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009343	dilated gallbladder		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009343	dilated gallbladder		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009493	abnormal cystic duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009498	abnormal extrahepatic bile duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009523	submandibular gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15093544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009535	abnormal skin sebaceous gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368895
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23999427
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009794	sebaceous gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009797	abnormal mismatch repair		IAGP		N	RGD:5509061	20200310	MGI			PMID:18264106
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20200310	MGI			PMID:17349585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010020	spleen vascular congestion		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17540175
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029981
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24430184
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25813352
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:26095252
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27462406
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:2891865
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:8152802
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20201112	MGI			PMID:30686754
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20210211	MGI			PMID:32767810
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27462406
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010273	increased classified tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19846776
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010274	increased organ/body region tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20080688
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010274	increased organ/body region tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21565614
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20697345
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010283	decreased classified tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21514245
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010285	decreased skin tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27462406
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17468755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23999427
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114584
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266220
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20200310	MGI			PMID:22034435
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010309	increased mesothelioma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010314	increased neurofibroma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010314	increased neurofibroma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19846776
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010315	increased cholangiocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17936562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010315	increased cholangiocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266220
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010315	increased cholangiocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010315	increased cholangiocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:29386660
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010322	increased cutaneous melanoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25252692
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010346	increased thyroid carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19351816
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010349	increased teratocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:11323676
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010363	increased fibrosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17607363
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20697345
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14699048
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14966562
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22932805
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20609353
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23999427
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010588	conotruncal ridge hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40133474
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010668	abnormal hepatic portal vein morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20200310	MGI			PMID:28294115
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010799	stomach mucosa hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23285300
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010856	dilated respiratory conducting tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010910	bronchiolar epithelial hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19151761
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010910	bronchiolar epithelial hyperplasia		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010943	abnormal bronchus epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010945	lung epithelium hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010945	lung epithelium hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832755
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010945	lung epithelium hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24276238
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0010952	abnormal fatty acid beta-oxidation		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011032	impaired branching involved in terminal bronchiole morphogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18059342
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20308544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25042889
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17476360
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230302	MGI			PMID:32552404
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18059342
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15093544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18059342
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16720837
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011702	abnormal fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22606359
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22892241
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20220428	MGI			PMID:31400748
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011861	increased cranium height		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:20179099
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200310	MGI			PMID:21576358
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200310	MGI			PMID:21576358
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012416	decreased gland tumor incidence		IAGP		N	RGD:5509061	20231102	MGI			PMID:36241718
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012416	decreased gland tumor incidence		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17486075
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012433	decreased ovarian tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20505730
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012546	triangular face		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15093544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:15894267
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:25042889
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:27032374
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013220	increased pancreas apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21056012
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013221	pancreatic acinar-to-ductal metaplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20807812
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013221	pancreatic acinar-to-ductal metaplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25042889
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013221	pancreatic acinar-to-ductal metaplasia		IAGP		N	RGD:5509061	20241024	MGI			PMID:31048544
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20200423	MGI			PMID:30858608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013331	abnormal lacrimal gland development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22745308
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013415	increased myeloid cell number in bone marrow		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013443	Harderian gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12957286
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25359213
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013733	squamous metaplasia of bulbourethral gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013735	squamous metaplasia of urethral gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18372904
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014076	absent Paneth cells		IAGP		N	RGD:5509061	20210225	MGI			PMID:30952657
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:14681207
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:17114584
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:22411819
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23285300
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20250814	MGI			PMID:18927348
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014754	abnormal tumor progression		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014754	abnormal tumor progression		IAGP		N	RGD:5509061	20260611	MGI			PMID:39986371
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:21317887
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:17369402
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:9334313
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260611	MGI			PMID:16720837
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0015003	decreased embryo length		IAGP		N	RGD:5509061	20260611	MGI			PMID:9294608
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0020190	abnormal lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25813352
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0030574	increased hair follicle cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21502497
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0030737	decreased glutamic acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31685994
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20251009	MGI			PMID:40848971
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17607363
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0031058	hepatosplenomegaly		IAGP		N	RGD:5509061	20200618	MGI			PMID:28846072
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0031159	abnormal hepatic portal vein thrombosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:17114585
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0031440	lymphatic vessel hypoplasia		IAGP		N	RGD:5509061	20220915	MGI			PMID:20179099
1550157	Kras	Kras proto-oncogene, GTPase	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15864294
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20201022	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20201022	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20240523	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20210826	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20221215	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20201022	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20221215	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20220519	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20201231	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0009454	impaired contextual conditioning behavior		IEA		N	RGD:5509061	20231207	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20240829	MGI			PMID:36943869
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20240829	MGI			PMID:36943869
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20240829	MGI			PMID:36943869
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240829	MGI			PMID:36943869
1550160	Ubl7	ubiquitin-like 7 (bone marrow stromal cell-derived)	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240829	MGI			PMID:36943869
1550161	Mxra8	matrix-remodelling associated 8	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1550161	Mxra8	matrix-remodelling associated 8	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1550161	Mxra8	matrix-remodelling associated 8	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20191212	MGI			PMID:31484075
1550161	Mxra8	matrix-remodelling associated 8	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550161	Mxra8	matrix-remodelling associated 8	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1550161	Mxra8	matrix-remodelling associated 8	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20191212	MGI			PMID:31484075
1550161	Mxra8	matrix-remodelling associated 8	gene	MP:0020941	decreased susceptibility to Togaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:31484075
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210826	MGI			
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33151556
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20210617	MGI			PMID:33151556
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33151556
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33151556
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20210617	MGI			PMID:33151556
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33151556
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0004534	decreased inner hair cell stereocilia number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33151556
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20211021	MGI			
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20210617	MGI			PMID:33151556
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20210617	MGI			PMID:33151556
1550162	Baiap2l2	BAI1-associated protein 2-like 2	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20240405	MGI			PMID:33151556
1550163	Abtb1	ankyrin repeat and BTB domain containing 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1550163	Abtb1	ankyrin repeat and BTB domain containing 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1550163	Abtb1	ankyrin repeat and BTB domain containing 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1550163	Abtb1	ankyrin repeat and BTB domain containing 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1550163	Abtb1	ankyrin repeat and BTB domain containing 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1550163	Abtb1	ankyrin repeat and BTB domain containing 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1550169	Asrgl1	asparaginase like 1	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550169	Asrgl1	asparaginase like 1	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20221222	MGI			PMID:35118070
1550171	Tpsg1	tryptase gamma 1	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210401	MGI			PMID:24821729
1550171	Tpsg1	tryptase gamma 1	gene	MP:0010896	decreased lung compliance		IAGP		N	RGD:5509061	20210401	MGI			PMID:24821729
1550171	Tpsg1	tryptase gamma 1	gene	MP:0010935	increased airway resistance		IAGP		N	RGD:5509061	20210401	MGI			PMID:24821729
1550171	Tpsg1	tryptase gamma 1	gene	MP:0010950	abnormal lung hysteresivity		IAGP		N	RGD:5509061	20210401	MGI			PMID:24821729
1550171	Tpsg1	tryptase gamma 1	gene	MP:0011044	increased lung elastance		IAGP		N	RGD:5509061	20210401	MGI			PMID:24821729
1550171	Tpsg1	tryptase gamma 1	gene	MP:0011047	increased lung tissue damping		IAGP		N	RGD:5509061	20210401	MGI			PMID:24821729
1550171	Tpsg1	tryptase gamma 1	gene	MP:0013299	decreased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20210401	MGI			PMID:24821729
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039842
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20201022	MGI			
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001423	abnormal liquid preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130538
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039842
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039842
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130538
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20251218	MGI			PMID:37253782
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25637356
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421388
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039842
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039842
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421388
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20251218	MGI			PMID:37253782
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20251218	MGI			PMID:37253782
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130538
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17599069
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421388
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421388
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421388
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421388
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421388
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421388
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421388
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20005824
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:25637356
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039842
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130538
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550173	Ehmt2	euchromatic histone lysine N-methyltransferase 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1550175	Cyp4a14	cytochrome P450, family 4, subfamily a, polypeptide 14	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320253
1550175	Cyp4a14	cytochrome P450, family 4, subfamily a, polypeptide 14	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320253
1550175	Cyp4a14	cytochrome P450, family 4, subfamily a, polypeptide 14	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320253
1550175	Cyp4a14	cytochrome P450, family 4, subfamily a, polypeptide 14	gene	MP:0005529	abnormal renal vascular resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320253
1550175	Cyp4a14	cytochrome P450, family 4, subfamily a, polypeptide 14	gene	MP:0005531	increased renal vascular resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320253
1550175	Cyp4a14	cytochrome P450, family 4, subfamily a, polypeptide 14	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320253
1550175	Cyp4a14	cytochrome P450, family 4, subfamily a, polypeptide 14	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11320253
1550179	Srgn	serglycin	gene	MP:0000336	decreased mast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15231821
1550179	Srgn	serglycin	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15231821
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0001063	abnormal trochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550181	Tubb3	tubulin, beta 3 class III	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074521
1550182	Pde8a	phosphodiesterase 8A	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IEA		N	RGD:5509061	20141003	MGI			
1550182	Pde8a	phosphodiesterase 8A	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20170105	MGI			
1550182	Pde8a	phosphodiesterase 8A	gene	MP:0003998	decreased thermal nociceptive threshold		IEA		N	RGD:5509061	20141003	MGI			
1550182	Pde8a	phosphodiesterase 8A	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172443
1550182	Pde8a	phosphodiesterase 8A	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21187369
1550182	Pde8a	phosphodiesterase 8A	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20170105	MGI			
1550182	Pde8a	phosphodiesterase 8A	gene	MP:0011385	abnormal testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172443
1550183	Atp6v0e2	ATPase, H+ transporting, lysosomal V0 subunit E2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20241121	MGI			
1550183	Atp6v0e2	ATPase, H+ transporting, lysosomal V0 subunit E2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0002905	decreased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550186	Clec2d	C-type lectin domain family 2, member d	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:18782774
1550187	Rnase13	ribonuclease, RNase A family, 13 (non-active)	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20210520	MGI			
1550187	Rnase13	ribonuclease, RNase A family, 13 (non-active)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1550187	Rnase13	ribonuclease, RNase A family, 13 (non-active)	gene	MP:0003883	enlarged stomach		IEA		N	RGD:5509061	20210520	MGI			
1550187	Rnase13	ribonuclease, RNase A family, 13 (non-active)	gene	MP:0011875	absent stomach		IEA		N	RGD:5509061	20210520	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9881978
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9881978
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20250508	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9881978
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9881978
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9881978
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9881978
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9881978
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20250508	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9881978
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14593101
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334369
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20250508	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334369
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17334369
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:14593101
1550192	Gcnt1	glucosaminyl (N-acetyl) transferase 1, core 2	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:17334369
1550193	Habp2	hyaluronic acid binding protein 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22989567
1550193	Habp2	hyaluronic acid binding protein 2	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22989567
1550193	Habp2	hyaluronic acid binding protein 2	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22989567
1550193	Habp2	hyaluronic acid binding protein 2	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22989567
1550196	Tigd3	tigger transposable element derived 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1550196	Tigd3	tigger transposable element derived 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20221215	MGI			
1550196	Tigd3	tigger transposable element derived 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1550196	Tigd3	tigger transposable element derived 3	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20220519	MGI			
1550197	Phaf1	phagosome assembly factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1550198	Nipa1	non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human)	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20200310	MGI			
1550199	Txnl1	thioredoxin-like 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1550199	Txnl1	thioredoxin-like 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1550199	Txnl1	thioredoxin-like 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1550199	Txnl1	thioredoxin-like 1	gene	MP:0001340	abnormal eyelid morphology		IEA		N	RGD:5509061	20230119	MGI			
1550199	Txnl1	thioredoxin-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230126	MGI			PMID:19349280
1550199	Txnl1	thioredoxin-like 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1550199	Txnl1	thioredoxin-like 1	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1550199	Txnl1	thioredoxin-like 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1550199	Txnl1	thioredoxin-like 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1550199	Txnl1	thioredoxin-like 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230119	MGI			
1550200	Panx2	pannexin 2	gene	MP:0001102	small superior vagus ganglion		IEA		N	RGD:5509061	20181227	MGI			
1550200	Panx2	pannexin 2	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22147915
1550200	Panx2	pannexin 2	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20181227	MGI			
1550200	Panx2	pannexin 2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1550200	Panx2	pannexin 2	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22147915
1550200	Panx2	pannexin 2	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22147915
1550200	Panx2	pannexin 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1550200	Panx2	pannexin 2	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20181227	MGI			
1550205	Tyw1	tRNA-yW synthesizing protein 1 homolog (S. cerevisiae)	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1550205	Tyw1	tRNA-yW synthesizing protein 1 homolog (S. cerevisiae)	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1550205	Tyw1	tRNA-yW synthesizing protein 1 homolog (S. cerevisiae)	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1550205	Tyw1	tRNA-yW synthesizing protein 1 homolog (S. cerevisiae)	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1550205	Tyw1	tRNA-yW synthesizing protein 1 homolog (S. cerevisiae)	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1550205	Tyw1	tRNA-yW synthesizing protein 1 homolog (S. cerevisiae)	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1550205	Tyw1	tRNA-yW synthesizing protein 1 homolog (S. cerevisiae)	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20201022	MGI			
1550206	Ttc17	tetratricopeptide repeat domain 17	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1550206	Ttc17	tetratricopeptide repeat domain 17	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1550206	Ttc17	tetratricopeptide repeat domain 17	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20181129	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514245
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514245
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001215	skin hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887817
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887817
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001717	absent ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19219045
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19219045
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20220203	MGI			PMID:21527500
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220203	MGI			PMID:21527500
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220203	MGI			PMID:21527500
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514245
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19219045
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887817
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20220203	MGI			PMID:21527500
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19219045
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20220203	MGI			PMID:21527500
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23945236
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0008526	decreased cranium width		IAGP		N	RGD:5509061	20180621	MGI			PMID:29590634
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514245
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0009819	abnormal circulating androgen level		IAGP		N	RGD:5509061	20220203	MGI			PMID:21527500
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20150910	MGI			PMID:18952847
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0010160	increased oligodendrocyte number		IAGP		N	RGD:5509061	20180621	MGI			PMID:29590634
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0010234	abnormal vibrissa follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0010283	decreased classified tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21514245
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0010457	pulmonary artery stenosis		IAGP		N	RGD:5509061	20180621	MGI			PMID:29590634
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16887817
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19219045
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0011385	abnormal testosterone level		IAGP		N	RGD:5509061	20220203	MGI			PMID:21527500
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0011812	increased cranium length		IAGP		N	RGD:5509061	20180621	MGI			PMID:29590634
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20180621	MGI			PMID:29590634
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0012065	increased astrocyte number		IAGP		N	RGD:5509061	20180621	MGI			PMID:29590634
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10209122
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0014269	decreased testes secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:21527500
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0030166	increased inner canthal distance		IAGP		N	RGD:5509061	20180621	MGI			PMID:29590634
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0030575	decreased hair follicle cell proliferation		IAGP		N	RGD:5509061	20181129	MGI			PMID:17419998
1550208	Map2k1	mitogen-activated protein kinase kinase 1	gene	MP:0031436	decreased copulatory plug deposition		IAGP		N	RGD:5509061	20220922	MGI			PMID:21527500
1550211	Cdk19	cyclin dependent kinase 19	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1550211	Cdk19	cyclin dependent kinase 19	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20220428	MGI			PMID:35110726
1550211	Cdk19	cyclin dependent kinase 19	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20220428	MGI			PMID:35110726
1550211	Cdk19	cyclin dependent kinase 19	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20220428	MGI			PMID:35110726
1550211	Cdk19	cyclin dependent kinase 19	gene	MP:0013705	decreased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20220428	MGI			PMID:35110726
1550212	Best3	bestrophin 3	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0004044	aortic dissection		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0006278	aortic aneurysm		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0010139	aortitis		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0010470	dilated ascending aorta		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0010473	descending aorta dilation		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0010658	thoracic aorta aneurysm		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0010659	abdominal aorta aneurysm		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550212	Best3	bestrophin 3	gene	MP:0010997	decreased aorta wall thickness		IAGP		N	RGD:5509061	20231019	MGI			PMID:37203562
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20240328	MGI			PMID:939824
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25762570
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240523	MGI			PMID:3593827
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:25762570
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:25762570
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002297	abnormal forced expiratory flow rates		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20240523	MGI			PMID:3593827
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002673	abnormal sperm number		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20240328	MGI			PMID:939824
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20240328	MGI			PMID:5713631
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0009856	failure of ejaculation		IAGP		N	RGD:5509061	20240523	MGI			PMID:3593827
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0010471	supravalvar aortic stenosis		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0010493	abnormal atrium myocardium morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0010943	abnormal bronchus epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25762570
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0011926	abnormal heart valve physiology		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20250925	MGI			PMID:38300707
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0014274	decreased respiration		IAGP		N	RGD:5509061	20230810	MGI			PMID:25762570
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0030775	abnormal calcaneal tendon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0030803	abnormal tendon cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30738849
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0031628	abnormal intromission		IAGP		N	RGD:5509061	20240711	MGI			PMID:3593827
1550215	Adamtsl2	ADAMTS-like 2	gene	MP:0031646	impotence		IAGP		N	RGD:5509061	20240822	MGI			PMID:3593827
1550216	Matn1	matrilin 1, cartilage matrix protein	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1550216	Matn1	matrilin 1, cartilage matrix protein	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1550216	Matn1	matrilin 1, cartilage matrix protein	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10633862
1550216	Matn1	matrilin 1, cartilage matrix protein	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1550216	Matn1	matrilin 1, cartilage matrix protein	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1550216	Matn1	matrilin 1, cartilage matrix protein	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1550216	Matn1	matrilin 1, cartilage matrix protein	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1550216	Matn1	matrilin 1, cartilage matrix protein	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20210812	MGI			PMID:27573814
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20160804	MGI			
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544477
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544477
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544477
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544477
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544477
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20160804	MGI			
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544477
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544477
1550217	Trrap	transformation/transcription domain-associated protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:16574947
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24646470
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16574947
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0004152	abnormal circulating iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16574947
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16574947
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24646470
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16574947
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20053755
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24646470
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390527
1550218	Hamp	hepcidin antimicrobial peptide	gene	MP:0011890	increased circulating ferritin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16574947
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11675330
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15484191
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20111116	MGI			
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18439426
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11675330
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15484191
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548595
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18439426
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11675330
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884450
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11675330
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11675330
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548595
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20230720	MGI			
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11675330
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0008345	abnormal gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548595
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884450
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0008349	abnormal gamma-delta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884450
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548595
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18439426
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0008363	decreased CD8-positive, gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884450
1550219	Ccr9	C-C motif chemokine receptor 9	gene	MP:0008399	abnormal alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18439426
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20111116	MGI			
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0002084	abnormal developmental patterning		IEA		N	RGD:5509061	20111116	MGI			
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20190912	MGI			PMID:30872163
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20190912	MGI			PMID:30872163
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:30872163
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0004180	failure of initiation of embryo turning		IEA		N	RGD:5509061	20111116	MGI			
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0004187	cardia bifida		IEA		N	RGD:5509061	20111116	MGI			
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20190912	MGI			PMID:30872163
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20111116	MGI			
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20190912	MGI			PMID:30872163
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20190912	MGI			PMID:30872163
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1550222	Alg13	asparagine-linked glycosylation 13	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1550230	Tnfrsf12a	tumor necrosis factor receptor superfamily, member 12a	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16424220
1550230	Tnfrsf12a	tumor necrosis factor receptor superfamily, member 12a	gene	MP:0010042	abnormal oval cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16110324
1550234	Senp7	SUMO1/sentrin specific peptidase 7	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1550234	Senp7	SUMO1/sentrin specific peptidase 7	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200310	MGI			
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0008957	abnormal placenta junctional zone morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550238	Fbxl12	F-box and leucine-rich repeat protein 12	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160818	MGI			PMID:26124079
1550240	Septin5	septin 5	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1550240	Septin5	septin 5	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20200402	MGI			
1550240	Septin5	septin 5	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1550240	Septin5	septin 5	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240081
1550240	Septin5	septin 5	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240081
1550240	Septin5	septin 5	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240081
1550240	Septin5	septin 5	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240081
1550240	Septin5	septin 5	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1550240	Septin5	septin 5	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20200402	MGI			
1550240	Septin5	septin 5	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1550240	Septin5	septin 5	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20200402	MGI			
1550240	Septin5	septin 5	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880646
1550240	Septin5	septin 5	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19240081
1550240	Septin5	septin 5	gene	MP:0009586	increased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11880646
1550240	Septin5	septin 5	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1550240	Septin5	septin 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550241	Ankle1	ankyrin repeat and LEM domain containing 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1550241	Ankle1	ankyrin repeat and LEM domain containing 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200310	MGI			
1550241	Ankle1	ankyrin repeat and LEM domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:27010503
1550241	Ankle1	ankyrin repeat and LEM domain containing 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:27010503
1550246	Lrwd1	leucine-rich repeats and WD repeat domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260305	MGI			PMID:35451548
1550246	Lrwd1	leucine-rich repeats and WD repeat domain containing 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260305	MGI			PMID:35451548
1550246	Lrwd1	leucine-rich repeats and WD repeat domain containing 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260305	MGI			PMID:35451548
1550246	Lrwd1	leucine-rich repeats and WD repeat domain containing 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20260305	MGI			PMID:35451548
1550246	Lrwd1	leucine-rich repeats and WD repeat domain containing 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20260305	MGI			PMID:35451548
1550246	Lrwd1	leucine-rich repeats and WD repeat domain containing 1	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20260305	MGI			PMID:35451548
1550247	Wdr36	WD repeat domain 36	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1550247	Wdr36	WD repeat domain 36	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20200310	MGI			PMID:21051332
1550247	Wdr36	WD repeat domain 36	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220811	MGI			
1550247	Wdr36	WD repeat domain 36	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1550247	Wdr36	WD repeat domain 36	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21051332
1550247	Wdr36	WD repeat domain 36	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550247	Wdr36	WD repeat domain 36	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1550247	Wdr36	WD repeat domain 36	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550249	Cd2ap	CD2-associated protein	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764198
1550249	Cd2ap	CD2-associated protein	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764198
1550249	Cd2ap	CD2-associated protein	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764198
1550249	Cd2ap	CD2-associated protein	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764198
1550249	Cd2ap	CD2-associated protein	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1550249	Cd2ap	CD2-associated protein	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20201217	MGI			PMID:30612599
1550249	Cd2ap	CD2-associated protein	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764198
1550249	Cd2ap	CD2-associated protein	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10514378
1550249	Cd2ap	CD2-associated protein	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12764198
1550251	Klhdc8b	kelch domain containing 8B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20231207	MGI			
1550252	Snx33	sorting nexin 33	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1550252	Snx33	sorting nexin 33	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550253	Adgrg5	adhesion G protein-coupled receptor G5	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1550253	Adgrg5	adhesion G protein-coupled receptor G5	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1550254	Ddx19a	DEAD box helicase 19a	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210506	MGI			PMID:30699353
1550257	Mon1a	MON1 homolog A, secretory traffciking associated	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1550257	Mon1a	MON1 homolog A, secretory traffciking associated	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1550257	Mon1a	MON1 homolog A, secretory traffciking associated	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1550257	Mon1a	MON1 homolog A, secretory traffciking associated	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1550257	Mon1a	MON1 homolog A, secretory traffciking associated	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550262	Ppp2r1a	protein phosphatase 2, regulatory subunit A, alpha	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791616
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0011261	abnormal limb mesenchyme morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0011685	abnormal limb paddle morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:37228654
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0013213	abnormal embryonic neuroepithelium primary cilium morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550264	Dync2i2	dynein 2 intermediate chain 2	gene	MP:0020850	abnormal microtubule cytoskeleton morphology		IAGP		N	RGD:5509061	20210225	MGI			PMID:28379358
1550265	Idh3b	isocitrate dehydrogenase 3 (NAD+) beta	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1550265	Idh3b	isocitrate dehydrogenase 3 (NAD+) beta	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1550265	Idh3b	isocitrate dehydrogenase 3 (NAD+) beta	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1550265	Idh3b	isocitrate dehydrogenase 3 (NAD+) beta	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1550265	Idh3b	isocitrate dehydrogenase 3 (NAD+) beta	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1550265	Idh3b	isocitrate dehydrogenase 3 (NAD+) beta	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20201022	MGI			
1550266	Pgf	placental growth factor	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003333
1550266	Pgf	placental growth factor	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11329059
1550266	Pgf	placental growth factor	gene	MP:0001619	abnormal vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12150967
1550266	Pgf	placental growth factor	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11329059
1550266	Pgf	placental growth factor	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11329059
1550266	Pgf	placental growth factor	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003333
1550266	Pgf	placental growth factor	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17051153
1550266	Pgf	placental growth factor	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12393422
1550266	Pgf	placental growth factor	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20241121	MGI			
1550266	Pgf	placental growth factor	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003333
1550266	Pgf	placental growth factor	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003333
1550266	Pgf	placental growth factor	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003333
1550266	Pgf	placental growth factor	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003333
1550266	Pgf	placental growth factor	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003333
1550266	Pgf	placental growth factor	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17003333
1550269	Fnbp1l	formin binding protein 1-like	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1550269	Fnbp1l	formin binding protein 1-like	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1550269	Fnbp1l	formin binding protein 1-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23236378
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23236378
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0002310	decreased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23236378
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0005479	decreased circulating triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0005661	decreased circulating adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982743
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23236378
1550271	Arrdc3	arrestin domain containing 3	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20180125	MGI			PMID:21982743
1550272	Stn1	STN1, CST complex subunit	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20250828	MGI			PMID:37163605
1550272	Stn1	STN1, CST complex subunit	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20250828	MGI			PMID:37163605
1550272	Stn1	STN1, CST complex subunit	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20250828	MGI			PMID:37163605
1550272	Stn1	STN1, CST complex subunit	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20250828	MGI			PMID:37163605
1550272	Stn1	STN1, CST complex subunit	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20250828	MGI			PMID:37163605
1550272	Stn1	STN1, CST complex subunit	gene	MP:0014040	increased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20250828	MGI			PMID:37163605
1550272	Stn1	STN1, CST complex subunit	gene	MP:0014755	increased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:37163605
1550272	Stn1	STN1, CST complex subunit	gene	MP:0014758	decreased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:37163605
1550272	Stn1	STN1, CST complex subunit	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20250828	MGI			PMID:37163605
1550273	Smad5	SMAD family member 5	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677256
1550273	Smad5	SMAD family member 5	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677256
1550273	Smad5	SMAD family member 5	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677256
1550273	Smad5	SMAD family member 5	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0001749	suppressed circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819941
1550273	Smad5	SMAD family member 5	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404080
1550273	Smad5	SMAD family member 5	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967875
1550273	Smad5	SMAD family member 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404080
1550273	Smad5	SMAD family member 5	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819941
1550273	Smad5	SMAD family member 5	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0002208	abnormal germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0002976	vascular smooth muscle hypotrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967875
1550273	Smad5	SMAD family member 5	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677256
1550273	Smad5	SMAD family member 5	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456754
1550273	Smad5	SMAD family member 5	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14502571
1550273	Smad5	SMAD family member 5	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456754
1550273	Smad5	SMAD family member 5	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967875
1550273	Smad5	SMAD family member 5	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967875
1550273	Smad5	SMAD family member 5	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967875
1550273	Smad5	SMAD family member 5	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404080
1550273	Smad5	SMAD family member 5	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0008393	absent primordial germ cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967875
1550273	Smad5	SMAD family member 5	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0009649	delayed embryo implantation		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0009656	delayed chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0009662	abnormal uterine receptivity		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0009666	abnormal embryo attachment		IAGP		N	RGD:5509061	20220630	MGI			PMID:35383354
1550273	Smad5	SMAD family member 5	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:16765933
1550273	Smad5	SMAD family member 5	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079226
1550273	Smad5	SMAD family member 5	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677256
1550273	Smad5	SMAD family member 5	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456754
1550273	Smad5	SMAD family member 5	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:10079220
1550273	Smad5	SMAD family member 5	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19819941
1550274	Trappc4	trafficking protein particle complex 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1550274	Trappc4	trafficking protein particle complex 4	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20231207	MGI			
1550274	Trappc4	trafficking protein particle complex 4	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20231207	MGI			
1550274	Trappc4	trafficking protein particle complex 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20151126	MGI			PMID:24966089
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178979
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22184322
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20151126	MGI			PMID:24966089
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22184322
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0002959	increased urine microalbumin level		IEA		N	RGD:5509061	20260402	MGI			
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:22184322
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22184322
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0005633	increased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22184322
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20151126	MGI			PMID:24966089
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22184322
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20151126	MGI			PMID:24966089
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0011131	abnormal lung endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178979
1550275	Cyp2c23	cytochrome P450, family 2, subfamily c, polypeptide 23	gene	MP:0011140	decreased lung endothelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20178979
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0009925	increased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0013802	abnormal IgG2 level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0014351	abnormal spleen B cell follicle shape		IAGP		N	RGD:5509061	20240104	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0020174	abnormal IgG level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550278	Adgrg3	adhesion G protein-coupled receptor G3	gene	MP:0020175	abnormal IgG1 level		IAGP		N	RGD:5509061	20160218	MGI			PMID:24113187
1550281	Mical3	microtubule associated monooxygenase, calponin and LIM domain containing 3	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1550281	Mical3	microtubule associated monooxygenase, calponin and LIM domain containing 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1550281	Mical3	microtubule associated monooxygenase, calponin and LIM domain containing 3	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1550281	Mical3	microtubule associated monooxygenase, calponin and LIM domain containing 3	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550281	Mical3	microtubule associated monooxygenase, calponin and LIM domain containing 3	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142319
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200820	MGI			PMID:31779270
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574395
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574395
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220811	MGI			PMID:35574006
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230119	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21163256
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142319
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574395
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220811	MGI			PMID:35574006
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142319
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21163256
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002212	abnormal secondary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142319
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20200820	MGI			PMID:31779270
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21163256
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200820	MGI			PMID:31779270
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002776	increased Sertoli cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002776	increased Sertoli cell number		IAGP		N	RGD:5509061	20160526	MGI			PMID:24803656
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142319
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002782	abnormal testes secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829911
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919750
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574395
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829911
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16877546
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004182	abnormal spermiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21163256
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919750
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16484321
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574395
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21163256
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21163256
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230119	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142319
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:35574006
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19838304
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:31779270
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20220811	MGI			PMID:35574006
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20230119	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919750
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20230119	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006241	abnormal placement of pupils		IEA		N	RGD:5509061	20230119	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006307	abnormal seminiferous tubule size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006308	enlarged seminiferous tubules		IAGP		N	RGD:5509061	20200820	MGI			PMID:31779270
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21163256
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006418	abnormal testis cord formation		IAGP		N	RGD:5509061	20200820	MGI			PMID:31779270
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006428	ectopic Sertoli cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0006428	ectopic Sertoli cells		IAGP		N	RGD:5509061	20200820	MGI			PMID:31779270
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107499
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142319
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22829911
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20230119	MGI			
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0013598	Leydig cell hypertrophy		IAGP		N	RGD:5509061	20150319	MGI			PMID:19574395
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20150312	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20150312	MGI			PMID:21163256
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:17591950
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:14745012
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19071104
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:21163256
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0020142	increased anti-sperm antibody level		IAGP		N	RGD:5509061	20160616	MGI			PMID:24803656
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0020355	abnormal Sertoli cell barrier morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0020355	abnormal Sertoli cell barrier morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0020356	abnormal Sertoli cell barrier function		IAGP		N	RGD:5509061	20160915	MGI			PMID:24803656
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0020356	abnormal Sertoli cell barrier function		IAGP		N	RGD:5509061	20220616	MGI			PMID:26265072
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0020356	abnormal Sertoli cell barrier function		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0020847	abnormal peroxisome physiology		IAGP		N	RGD:5509061	20230615	MGI			PMID:22829911
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:36718792
1550285	Plekha5	pleckstrin homology domain containing A5	gene	MP:0031407	increased Sertoli cell proliferation		IAGP		N	RGD:5509061	20220630	MGI			PMID:19071104
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15634781
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:15634781
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200402	MGI			
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15634781
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200310	MGI			
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:15634781
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15634781
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:15634781
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20200310	MGI			PMID:15634781
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20200310	MGI			
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15634781
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15665098
1550286	Aph1a	aph1 homolog A, gamma secretase subunit	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505171
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183677
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529747
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12933578
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529747
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529747
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0004898	uterine hemorrhage		IAGP		N	RGD:5509061	20150827	MGI			PMID:12933578
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0004898	uterine hemorrhage		IAGP		N	RGD:5509061	20150827	MGI			PMID:17183677
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0004898	uterine hemorrhage		IAGP		N	RGD:5509061	20150827	MGI			PMID:18224415
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0005243	hemothorax		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529747
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0005243	hemothorax		IAGP		N	RGD:5509061	20141003	MGI			PMID:12933578
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529747
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529747
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20150827	MGI			PMID:18224415
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529747
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20150827	MGI			PMID:12933578
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20150827	MGI			PMID:18224415
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12529747
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505171
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183677
1550288	F13a1	coagulation factor XIII, A1 subunit	gene	MP:0031152	subcutaneous hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:12529747
1550289	Msx3	msh homeobox 3	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1550289	Msx3	msh homeobox 3	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20220519	MGI			
1550294	Rcor1	REST corepressor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652990
1550294	Rcor1	REST corepressor 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652990
1550294	Rcor1	REST corepressor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652990
1550294	Rcor1	REST corepressor 1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652990
1550294	Rcor1	REST corepressor 1	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:24652990
1550296	Taok2	TAO kinase 2	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20200310	MGI			
1550296	Taok2	TAO kinase 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1550296	Taok2	TAO kinase 2	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:22883308
1550296	Taok2	TAO kinase 2	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1550296	Taok2	TAO kinase 2	gene	MP:0008221	abnormal hippocampal commissure morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1550296	Taok2	TAO kinase 2	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1550296	Taok2	TAO kinase 2	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22883308
1550296	Taok2	TAO kinase 2	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:22883308
1550296	Taok2	TAO kinase 2	gene	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20200310	MGI			PMID:22883308
1550296	Taok2	TAO kinase 2	gene	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20200310	MGI			PMID:22883308
1550296	Taok2	TAO kinase 2	gene	MP:0011617	abnormal habituation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22883308
1550296	Taok2	TAO kinase 2	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:22883308
1550296	Taok2	TAO kinase 2	gene	MP:0012443	increased corpus callosum size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1550296	Taok2	TAO kinase 2	gene	MP:0012450	decreased primary motor cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1550296	Taok2	TAO kinase 2	gene	MP:0012473	increased cingulate cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1550298	Art5	ADP-ribosyltransferase 5	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20210520	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001697	abnormal embryo size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001706	abnormal left-right axis patterning		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20211021	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0009806	abnormal otic vesicle morphology		IEA		N	RGD:5509061	20190502	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1550299	Pigq	phosphatidylinositol glycan anchor biosynthesis, class Q	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1550300	Ift80	intraflagellar transport 80	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0000552	abnormal radius morphology		IEA		N	RGD:5509061	20201231	MGI			
1550300	Ift80	intraflagellar transport 80	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:26053317
1550300	Ift80	intraflagellar transport 80	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20200310	MGI			
1550300	Ift80	intraflagellar transport 80	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0005108	abnormal ulna morphology		IEA		N	RGD:5509061	20201231	MGI			
1550300	Ift80	intraflagellar transport 80	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1550300	Ift80	intraflagellar transport 80	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21227999
1550300	Ift80	intraflagellar transport 80	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550300	Ift80	intraflagellar transport 80	gene	MP:0013206	abnormal motile cilium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26053317
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20260101	MGI			PMID:23549079
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20230601	MGI			PMID:24371506
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878566
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20111116	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20111116	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878566
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20230601	MGI			PMID:24371506
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878566
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218620
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20160609	MGI			PMID:25368181
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832054
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190743
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146240
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521762
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21665954
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230601	MGI			PMID:24371506
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973973
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20230601	MGI			PMID:24371506
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146240
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146240
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002711	decreased glucagon secretion		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12881419
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002759	abnormal caudal vertebrae morphology		IEA		N	RGD:5509061	20220811	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20111116	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20160609	MGI			PMID:25368181
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218620
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0003030	acidemia		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12881419
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218620
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20160609	MGI			PMID:25368181
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20251218	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12881419
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146240
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21665954
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218620
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146240
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832054
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218620
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20160609	MGI			PMID:25368181
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20160609	MGI			PMID:25368181
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218620
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224388
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521762
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218620
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20160609	MGI			PMID:25368181
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20251218	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12881419
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832054
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12881419
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005662	increased circulating adrenaline level		IAGP		N	RGD:5509061	20251218	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521762
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:18174367
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190743
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20230601	MGI			PMID:24371506
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878566
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0009455	enhanced cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878566
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832054
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878566
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10973973
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21216955
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20160609	MGI			PMID:25368181
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0012557	decreased calcium uptake by cardiac muscle		IAGP		N	RGD:5509061	20160609	MGI			PMID:25368181
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:21878566
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0030588	decreased pancreatic alpha cell mass		IAGP		N	RGD:5509061	20251211	MGI			PMID:39420001
1550302	Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	gene	MP:0031717	prolonged corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:39420001
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20190502	MGI			
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0006204	embryonic lethality before implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728759
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1550306	Kat5	K(lysine) acetyltransferase 5	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:17728759
1550307	Paqr8	progestin and adipoQ receptor family member VIII	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
1550307	Paqr8	progestin and adipoQ receptor family member VIII	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210128	MGI			
1550313	Lrrfip1	leucine rich repeat (in FLII) interacting protein 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1550313	Lrrfip1	leucine rich repeat (in FLII) interacting protein 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20250508	MGI			
1550313	Lrrfip1	leucine rich repeat (in FLII) interacting protein 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1550313	Lrrfip1	leucine rich repeat (in FLII) interacting protein 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1550313	Lrrfip1	leucine rich repeat (in FLII) interacting protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550313	Lrrfip1	leucine rich repeat (in FLII) interacting protein 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1550314	Ociad1	OCIA domain containing 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1550314	Ociad1	OCIA domain containing 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1550314	Ociad1	OCIA domain containing 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0011181	increased hematopoietic cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0011898	abnormal platelet cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0013415	increased myeloid cell number in bone marrow		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550314	Ociad1	OCIA domain containing 1	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30952670
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20240919	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20240919	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20240919	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20240919	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20240919	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550318	Eipr1	EARP complex and GARP complex interacting protein 1	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241128	MGI			
1550321	Pcdh12	protocadherin 12	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20251127	MGI			
1550321	Pcdh12	protocadherin 12	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1550321	Pcdh12	protocadherin 12	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15541725
1550322	Elmod2	ELMO/CED-12 domain containing 2	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20200310	MGI			
1550322	Elmod2	ELMO/CED-12 domain containing 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1550322	Elmod2	ELMO/CED-12 domain containing 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20200310	MGI			
1550322	Elmod2	ELMO/CED-12 domain containing 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1550322	Elmod2	ELMO/CED-12 domain containing 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20200310	MGI			
1550322	Elmod2	ELMO/CED-12 domain containing 2	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20200310	MGI			
1550322	Elmod2	ELMO/CED-12 domain containing 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20200310	MGI			
1550322	Elmod2	ELMO/CED-12 domain containing 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200310	MGI			
1550323	Dcaf10	DDB1 and CUL4 associated factor 10	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1550323	Dcaf10	DDB1 and CUL4 associated factor 10	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20200310	MGI			
1550323	Dcaf10	DDB1 and CUL4 associated factor 10	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201231	MGI			
1550323	Dcaf10	DDB1 and CUL4 associated factor 10	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200310	MGI			
1550323	Dcaf10	DDB1 and CUL4 associated factor 10	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20210520	MGI			
1550323	Dcaf10	DDB1 and CUL4 associated factor 10	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1550327	Adgrf3	adhesion G protein-coupled receptor F3	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240613	MGI			PMID:38697008
1550330	Taar4	trace amine-associated receptor 4	gene	MP:0001983	abnormal olfactory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624375
1550330	Taar4	trace amine-associated receptor 4	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624375
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0008431	abnormal short-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0011396	abnormal sleep behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22072671
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:31582721
1550331	Lrrc7	leucine rich repeat containing 7	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22072671
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20180301	MGI			PMID:27269051
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20180301	MGI			PMID:27269051
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:27269051
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0004525	thin cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20180301	MGI			PMID:27269051
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:27269051
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:27269051
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0004534	decreased inner hair cell stereocilia number		IAGP		N	RGD:5509061	20180301	MGI			PMID:27269051
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20180301	MGI			PMID:27269051
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20180301	MGI			PMID:27269051
1550332	Ripor2	RHO family interacting cell polarization regulator 2	gene	MP:0031674	long inner hair cell stereocilia		IAGP		N	RGD:5509061	20250814	MGI			PMID:27269051
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19168544
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19168544
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19168544
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19168544
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550333	Eif2s2	eukaryotic translation initiation factor 2 subunit 2 beta	gene	MP:0030934	decreased primordial germ cell proliferation		IAGP		N	RGD:5509061	20190411	MGI			PMID:19168544
1550334	Cops3	COP9 signalosome subunit 3	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972600
1550334	Cops3	COP9 signalosome subunit 3	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972600
1550334	Cops3	COP9 signalosome subunit 3	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972600
1550334	Cops3	COP9 signalosome subunit 3	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972600
1550334	Cops3	COP9 signalosome subunit 3	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972600
1550334	Cops3	COP9 signalosome subunit 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972600
1550334	Cops3	COP9 signalosome subunit 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972600
1550334	Cops3	COP9 signalosome subunit 3	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972600
1550334	Cops3	COP9 signalosome subunit 3	gene	MP:0011197	abnormal proamniotic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12972600
1550335	Tmem38a	transmembrane protein 38A	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550335	Tmem38a	transmembrane protein 38A	gene	MP:0004085	abnormal heartbeat		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550335	Tmem38a	transmembrane protein 38A	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550335	Tmem38a	transmembrane protein 38A	gene	MP:0004567	decreased myocardial fiber number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550335	Tmem38a	transmembrane protein 38A	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550335	Tmem38a	transmembrane protein 38A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9875844
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10786799
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9875844
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360556
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10786799
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10786799
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10786799
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716994
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16757976
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360556
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713479
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587764
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9875844
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713479
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17713479
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587764
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716994
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716994
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16670198
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360556
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172844
1550337	Xrcc4	X-ray repair complementing 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9875844
1550338	Krt75	keratin 75	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17851587
1550338	Krt75	keratin 75	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17851587
1550338	Krt75	keratin 75	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17851587
1550338	Krt75	keratin 75	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17851587
1550338	Krt75	keratin 75	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17851587
1550338	Krt75	keratin 75	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17851587
1550338	Krt75	keratin 75	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17851587
1550338	Krt75	keratin 75	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1550338	Krt75	keratin 75	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17851587
1550340	Arhgap11a	Rho GTPase activating protein 11A	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20221201	MGI			PMID:33938018
1550340	Arhgap11a	Rho GTPase activating protein 11A	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20221201	MGI			PMID:33938018
1550340	Arhgap11a	Rho GTPase activating protein 11A	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20221201	MGI			PMID:33938018
1550340	Arhgap11a	Rho GTPase activating protein 11A	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:33938018
1550340	Arhgap11a	Rho GTPase activating protein 11A	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:33938018
1550340	Arhgap11a	Rho GTPase activating protein 11A	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:33938018
1550340	Arhgap11a	Rho GTPase activating protein 11A	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20221201	MGI			PMID:33938018
1550340	Arhgap11a	Rho GTPase activating protein 11A	gene	MP:0020067	increased neocortex size		IAGP		N	RGD:5509061	20221201	MGI			PMID:33938018
1550341	Stk25	serine/threonine kinase 25 (yeast)	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24225308
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20141003	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0001539	decreased caudal vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0002697	abnormal eye size		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20141003	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20141003	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1550342	Pex3	peroxisomal biogenesis factor 3	gene	MP:0012725	small sebaceous gland		IAGP		N	RGD:5509061	20150709	MGI			PMID:24721909
1550343	Klf9	Kruppel-like transcription factor 9	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:12640131
1550343	Klf9	Kruppel-like transcription factor 9	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:12640131
1550345	Trim59	tripartite motif-containing 59	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0002583	absent extraembryonic ectoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20211021	MGI			
1550345	Trim59	tripartite motif-containing 59	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550345	Trim59	tripartite motif-containing 59	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0011209	absent extraembryonic coelom		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550345	Trim59	tripartite motif-containing 59	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1550345	Trim59	tripartite motif-containing 59	gene	MP:0012142	absent amniotic cavity		IAGP		N	RGD:5509061	20200310	MGI			PMID:29467473
1550347	Frmd6	FERM domain containing 6	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20181227	MGI			
1550347	Frmd6	FERM domain containing 6	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1550347	Frmd6	FERM domain containing 6	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1550347	Frmd6	FERM domain containing 6	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1550347	Frmd6	FERM domain containing 6	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20181227	MGI			
1550347	Frmd6	FERM domain containing 6	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1550347	Frmd6	FERM domain containing 6	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20181227	MGI			
1550347	Frmd6	FERM domain containing 6	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20181227	MGI			
1550347	Frmd6	FERM domain containing 6	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20250508	MGI			
1550350	Mrm2	mitochondrial rRNA methyltransferase 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1550350	Mrm2	mitochondrial rRNA methyltransferase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1550350	Mrm2	mitochondrial rRNA methyltransferase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550350	Mrm2	mitochondrial rRNA methyltransferase 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1550350	Mrm2	mitochondrial rRNA methyltransferase 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550351	Dnase1l1	deoxyribonuclease 1-like 1	gene	MP:0001405	impaired coordination		IEA		N	RGD:5509061	20111116	MGI			
1550352	Spmip8	sperm microtubule inner protein 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:12478613
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12478613
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11468145
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0008738	abnormal liver iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12478613
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19492434
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25629408
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10652280
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0011890	increased circulating ferritin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11468145
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1550357	Fth1	ferritin heavy polypeptide 1	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:19492434
1550360	Ubxn11	UBX domain protein 11	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1550362	Iah1	isoamyl acetate-hydrolyzing esterase 1 homolog	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1550362	Iah1	isoamyl acetate-hydrolyzing esterase 1 homolog	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20160421	MGI			
1550362	Iah1	isoamyl acetate-hydrolyzing esterase 1 homolog	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20190502	MGI			
1550362	Iah1	isoamyl acetate-hydrolyzing esterase 1 homolog	gene	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20201001	MGI			PMID:32407372
1550362	Iah1	isoamyl acetate-hydrolyzing esterase 1 homolog	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20160421	MGI			
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0003948	abnormal gas homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0008403	decreased cellular sensitivity to alkylating agent induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0008903	abnormal mesenteric fat pad morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20260402	MGI			
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0014174	decreased fatty acid beta-oxidation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0014398	abnormal fat cell mitochondrial morphology		IAGP		N	RGD:5509061	20240718	MGI			PMID:22433842
1550363	Oma1	OMA1 zinc metallopeptidase	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:22433842
1550364	Uqcrh	ubiquinol-cytochrome c reductase hinge protein	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20241121	MGI			
1550364	Uqcrh	ubiquinol-cytochrome c reductase hinge protein	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20241121	MGI			
1550364	Uqcrh	ubiquinol-cytochrome c reductase hinge protein	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20241121	MGI			
1550364	Uqcrh	ubiquinol-cytochrome c reductase hinge protein	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1550364	Uqcrh	ubiquinol-cytochrome c reductase hinge protein	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20241121	MGI			
1550364	Uqcrh	ubiquinol-cytochrome c reductase hinge protein	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20241121	MGI			
1550369	Vps36	vacuolar protein sorting 36	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20231207	MGI			
1550369	Vps36	vacuolar protein sorting 36	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210826	MGI			
1550369	Vps36	vacuolar protein sorting 36	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210826	MGI			
1550369	Vps36	vacuolar protein sorting 36	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20210826	MGI			
1550369	Vps36	vacuolar protein sorting 36	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1550370	Chrd	chordin	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1550370	Chrd	chordin	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1550370	Chrd	chordin	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1550370	Chrd	chordin	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1550370	Chrd	chordin	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1550370	Chrd	chordin	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1550370	Chrd	chordin	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001085	small petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001086	absent petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001089	absent nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1550370	Chrd	chordin	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1550370	Chrd	chordin	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1550370	Chrd	chordin	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1550370	Chrd	chordin	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0002252	abnormal oropharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0002256	abnormal laryngeal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1550370	Chrd	chordin	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247433
1550370	Chrd	chordin	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1550370	Chrd	chordin	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0003499	thyroid gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18550712
1550370	Chrd	chordin	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1550370	Chrd	chordin	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004387	abnormal prechordal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1550370	Chrd	chordin	gene	MP:0004422	small temporal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004450	presphenoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004541	absent auditory tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004544	absent esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004549	small trachea		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004554	small pharynx		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0004554	small pharynx		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004572	fusion of basioccipital and basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20170921	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15013800
1550370	Chrd	chordin	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1550370	Chrd	chordin	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1550370	Chrd	chordin	gene	MP:0004670	small vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0004899	absent temporal bone squamous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0004913	absent mandibular angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1550370	Chrd	chordin	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1550370	Chrd	chordin	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0006285	absent inner ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0006291	aprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0006295	absent sclerotome		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0008921	increased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0008926	abnormal anterior definitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1550370	Chrd	chordin	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1550370	Chrd	chordin	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0009899	hyoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0010335	fused first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:20508035
1550370	Chrd	chordin	gene	MP:0010657	absent pulmonary trunk		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0010663	abnormal brachiocephalic trunk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0010729	absent arcus anterior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17634368
1550370	Chrd	chordin	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0011238	abnormal inner ear development		IAGP		N	RGD:5509061	20240822	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0014517	abnormal outer ear development		IAGP		N	RGD:5509061	20240822	MGI			PMID:10688202
1550370	Chrd	chordin	gene	MP:0014517	abnormal outer ear development		IAGP		N	RGD:5509061	20240822	MGI			PMID:19247433
1550370	Chrd	chordin	gene	MP:0030375	short zygomatic arch		IAGP		N	RGD:5509061	20171207	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0030869	thyroid cartilage hypoplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:12810603
1550370	Chrd	chordin	gene	MP:0030874	cricoid cartilage hypoplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:12810603
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17310981
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20170803	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223418
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17310981
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25196150
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223418
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002213	true hermaphroditism		IAGP		N	RGD:5509061	20201224	MGI			PMID:17848526
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002748	abnormal pulmonary valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223418
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223418
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20201224	MGI			PMID:17848526
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0002996	ovotestis		IAGP		N	RGD:5509061	20201224	MGI			PMID:17848526
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0003808	increased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25196150
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20160304	MGI			PMID:25196150
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0006111	abnormal coronary circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0006123	tricuspid valve atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17310981
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0009573	abnormal right lung middle lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010224	abnormal heart ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20160304	MGI			PMID:25196150
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20160304	MGI			PMID:25196150
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010449	heart right ventricle outflow tract stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010449	heart right ventricle outflow tract stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010459	supravalvar pulmonary trunk stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010561	absent coronary vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010640	ventricular myocardium compact layer hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0010824	absent right lung accessory lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160304	MGI			PMID:25196150
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19411759
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103912
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20160304	MGI			PMID:25196150
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0013602	abnormal Leydig cell differentiation		IAGP		N	RGD:5509061	20150319	MGI			PMID:12223418
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0021155	abnormal heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:25196150
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231102	MGI			PMID:10892744
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0031525	thin left ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0031529	pulmonary valve hyperplasia		IAGP		N	RGD:5509061	20240118	MGI			PMID:10888889
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:25196150
1550372	Zfpm2	zinc finger protein, multitype 2	gene	MP:0031645	increased myocardial fiber apoptosis		IAGP		N	RGD:5509061	20250515	MGI			PMID:19411759
1550375	Rraga	Ras-related GTP binding A	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263183
1550375	Rraga	Ras-related GTP binding A	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263183
1550375	Rraga	Ras-related GTP binding A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263183
1550375	Rraga	Ras-related GTP binding A	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263183
1550375	Rraga	Ras-related GTP binding A	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263183
1550375	Rraga	Ras-related GTP binding A	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263183
1550375	Rraga	Ras-related GTP binding A	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263183
1550375	Rraga	Ras-related GTP binding A	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263183
1550375	Rraga	Ras-related GTP binding A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550375	Rraga	Ras-related GTP binding A	gene	MP:0020444	abnormal intestine apoptosis		IAGP		N	RGD:5509061	20181122	MGI			PMID:24768164
1550376	Wdr48	WD repeat domain 48	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550376	Wdr48	WD repeat domain 48	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24001775
1550377	Atp13a1	ATPase type 13A1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210826	MGI			
1550377	Atp13a1	ATPase type 13A1	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20220811	MGI			
1550377	Atp13a1	ATPase type 13A1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210826	MGI			
1550377	Atp13a1	ATPase type 13A1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210826	MGI			
1550377	Atp13a1	ATPase type 13A1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210826	MGI			
1550377	Atp13a1	ATPase type 13A1	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210826	MGI			
1550377	Atp13a1	ATPase type 13A1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241121	MGI			
1550377	Atp13a1	ATPase type 13A1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1550377	Atp13a1	ATPase type 13A1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20210826	MGI			
1550377	Atp13a1	ATPase type 13A1	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20210826	MGI			
1550378	Yap1	yes-associated protein 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0000524	decreased renal tubule number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:26109051
1550378	Yap1	yes-associated protein 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18332127
1550378	Yap1	yes-associated protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:18332127
1550378	Yap1	yes-associated protein 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0001721	absent visceral yolk sac blood islands		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18332127
1550378	Yap1	yes-associated protein 1	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:18332127
1550378	Yap1	yes-associated protein 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18332127
1550378	Yap1	yes-associated protein 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:22028467
1550378	Yap1	yes-associated protein 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:26699479
1550378	Yap1	yes-associated protein 1	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20260409	MGI			PMID:39185559
1550378	Yap1	yes-associated protein 1	gene	MP:0003046	liver cirrhosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0003252	abnormal bile duct physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26109051
1550378	Yap1	yes-associated protein 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26699479
1550378	Yap1	yes-associated protein 1	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0003624	anuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:26109051
1550378	Yap1	yes-associated protein 1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0004755	abnormal loop of Henle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22028467
1550378	Yap1	yes-associated protein 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:22028467
1550378	Yap1	yes-associated protein 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1550378	Yap1	yes-associated protein 1	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21041407
1550378	Yap1	yes-associated protein 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21041407
1550378	Yap1	yes-associated protein 1	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21041407
1550378	Yap1	yes-associated protein 1	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0009714	thin epidermis stratum basale		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:21041407
1550378	Yap1	yes-associated protein 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:21041407
1550378	Yap1	yes-associated protein 1	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:26109051
1550378	Yap1	yes-associated protein 1	gene	MP:0010500	myocardium hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0011004	abnormal epidermal stem cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21376238
1550378	Yap1	yes-associated protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918388
1550378	Yap1	yes-associated protein 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19289085
1550378	Yap1	yes-associated protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22028467
1550378	Yap1	yes-associated protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23555292
1550378	Yap1	yes-associated protein 1	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0012236	abnormal cholangiocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26699479
1550378	Yap1	yes-associated protein 1	gene	MP:0012740	abnormal posterior primitive streak morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16354681
1550378	Yap1	yes-associated protein 1	gene	MP:0013611	abnormal bile duct epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26109051
1550378	Yap1	yes-associated protein 1	gene	MP:0020359	abnormal ribbon synapse morphology		IAGP		N	RGD:5509061	20210708	MGI			PMID:32801350
1550378	Yap1	yes-associated protein 1	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:20643348
1550378	Yap1	yes-associated protein 1	gene	MP:0031216	decreased susceptibility to myocardial ischemic injury		IAGP		N	RGD:5509061	20260409	MGI			PMID:39185559
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20260402	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20241121	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20241121	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20260402	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20260402	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20260402	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0004733	abnormal thoracic cavity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19767744
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20260402	MGI			
1550380	Creb3l2	cAMP responsive element binding protein 3-like 2	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20260402	MGI			
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0003981	decreased circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20201022	MGI			
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0021133	increased amino acid betaine level		IAGP		N	RGD:5509061	20220721	MGI			PMID:21878621
1550381	Bhmt	betaine-homocysteine methyltransferase	gene	MP:0030753	decreased choline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:21878621
1550382	Itgal	integrin alpha L	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1550382	Itgal	integrin alpha L	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634125
1550382	Itgal	integrin alpha L	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1550382	Itgal	integrin alpha L	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634125
1550382	Itgal	integrin alpha L	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1550382	Itgal	integrin alpha L	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955836
1550382	Itgal	integrin alpha L	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955836
1550382	Itgal	integrin alpha L	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955185
1550382	Itgal	integrin alpha L	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955836
1550382	Itgal	integrin alpha L	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955836
1550382	Itgal	integrin alpha L	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16872848
1550382	Itgal	integrin alpha L	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023213
1550382	Itgal	integrin alpha L	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955185
1550382	Itgal	integrin alpha L	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008446
1550382	Itgal	integrin alpha L	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1550382	Itgal	integrin alpha L	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1550382	Itgal	integrin alpha L	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023213
1550382	Itgal	integrin alpha L	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847222
1550382	Itgal	integrin alpha L	gene	MP:0003627	abnormal leukocyte tethering or rolling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634125
1550382	Itgal	integrin alpha L	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1550382	Itgal	integrin alpha L	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634125
1550382	Itgal	integrin alpha L	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955836
1550382	Itgal	integrin alpha L	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008446
1550382	Itgal	integrin alpha L	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023213
1550382	Itgal	integrin alpha L	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955185
1550382	Itgal	integrin alpha L	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1550382	Itgal	integrin alpha L	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1550382	Itgal	integrin alpha L	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955836
1550382	Itgal	integrin alpha L	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023213
1550382	Itgal	integrin alpha L	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210787
1550382	Itgal	integrin alpha L	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9637488
1550382	Itgal	integrin alpha L	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955185
1550382	Itgal	integrin alpha L	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955836
1550382	Itgal	integrin alpha L	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15210787
1550382	Itgal	integrin alpha L	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1550382	Itgal	integrin alpha L	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30194420
1550382	Itgal	integrin alpha L	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10224287
1550382	Itgal	integrin alpha L	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955185
1550382	Itgal	integrin alpha L	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847222
1550382	Itgal	integrin alpha L	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847222
1550382	Itgal	integrin alpha L	gene	MP:0008599	increased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847222
1550382	Itgal	integrin alpha L	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847222
1550382	Itgal	integrin alpha L	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10528208
1550382	Itgal	integrin alpha L	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15955836
1550382	Itgal	integrin alpha L	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008446
1550382	Itgal	integrin alpha L	gene	MP:0020333	enhanced leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:20023213
1550382	Itgal	integrin alpha L	gene	MP:0030960	abnormal diapedesis		IAGP		N	RGD:5509061	20190725	MGI			PMID:20023213
1550384	Tube1	tubulin, epsilon 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20250508	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20240523	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20240523	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20250508	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1550384	Tube1	tubulin, epsilon 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20240523	MGI			
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24315444
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000561	adactyly		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24315444
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001428	adipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841259
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841259
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001679	thin apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841259
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841259
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841259
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841259
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24315444
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0004096	abnormal midbrain-hindbrain boundary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0004126	thin hypodermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005504	abnormal ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0006101	absent tegmentum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0006106	absent tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0008052	abnormal serous gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:24315444
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0009795	epidermal spongiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0011015	decreased body surface temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20231102	MGI			PMID:34587386
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841259
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246653
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20614471
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:22377357
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0031395	cutaneous mastocytosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:23918954
1550386	Wls	wntless WNT ligand secretion mediator	gene	MP:0031395	cutaneous mastocytosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:24315444
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210826	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210826	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20201022	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20241121	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210304	MGI			PMID:33483593
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20241121	MGI			
1550388	Larp1	La ribonucleoprotein 1, translational regulator	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1550391	Nup107	nucleoporin 107	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20180426	MGI			PMID:29363275
1550392	Hmgn2	high mobility group nucleosomal binding domain 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210422	MGI			
1550392	Hmgn2	high mobility group nucleosomal binding domain 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1550394	Abhd14b	abhydrolase domain containing 14b	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1550396	Kars1	lysyl-tRNA synthetase 1	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20201210	MGI			PMID:26091349
1550396	Kars1	lysyl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1550396	Kars1	lysyl-tRNA synthetase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
1550396	Kars1	lysyl-tRNA synthetase 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:26091349
1550397	Nudt2	nudix hydrolase 2	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20240425	MGI			PMID:34824277
1550397	Nudt2	nudix hydrolase 2	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20240425	MGI			PMID:34824277
1550401	Tll1	tolloid-like	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808086
1550401	Tll1	tolloid-like	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20200310	MGI			
1550401	Tll1	tolloid-like	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0000299	failure of atrioventricular cushion closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20200310	MGI			
1550401	Tll1	tolloid-like	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0003755	abnormal palate morphology		IEA		N	RGD:5509061	20200310	MGI			
1550401	Tll1	tolloid-like	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0004056	abnormal myocardium compact layer morphology		IEA		N	RGD:5509061	20200310	MGI			
1550401	Tll1	tolloid-like	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0004627	abnormal trochanter morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0004675	rib fractures		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0004987	abnormal osteoblast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808086
1550401	Tll1	tolloid-like	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808086
1550401	Tll1	tolloid-like	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0009868	abnormal descending thoracic aorta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20200310	MGI			
1550401	Tll1	tolloid-like	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808086
1550401	Tll1	tolloid-like	gene	MP:0010433	double inlet heart left ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808086
1550401	Tll1	tolloid-like	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10331975
1550401	Tll1	tolloid-like	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0013626	decreased femur yield load		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0013633	decreased femur maximal load		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0013638	decreased femur stiffness		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0013646	decreased energy dissipated prior to femur fracture		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0013941	abnormal enthesis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0030484	abnormal osteocyte lacuna morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0030487	abnormal osteocyte dendritic process morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550401	Tll1	tolloid-like	gene	MP:0030827	femur fracture		IAGP		N	RGD:5509061	20200310	MGI			PMID:24419319
1550402	Polk	polymerase (DNA directed), kappa	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16731053
1550402	Polk	polymerase (DNA directed), kappa	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12555660
1550403	Uroc1	urocanase domain containing 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1550403	Uroc1	urocanase domain containing 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20200310	MGI			
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0001875	testis inflammation		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0014631	abnormal elongated spermatid morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550404	Wfdc15a	WAP four-disulfide core domain 15A	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:39222051
1550407	Pus3	pseudouridine synthase 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20260402	MGI			
1550407	Pus3	pseudouridine synthase 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1550407	Pus3	pseudouridine synthase 3	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20260402	MGI			
1550407	Pus3	pseudouridine synthase 3	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20260402	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20240523	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20210520	MGI			PMID:31999954
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20230119	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230119	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20210520	MGI			PMID:31999954
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20230119	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20210520	MGI			PMID:31999954
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230119	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20230601	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0014384	increased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:31999954
1550408	Eif4g1	eukaryotic translation initiation factor 4, gamma 1	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20210520	MGI			PMID:31999954
1550409	Tmem37	transmembrane protein 37	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1550410	Chmp7	charged multivesicular body protein 7	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1550410	Chmp7	charged multivesicular body protein 7	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1550410	Chmp7	charged multivesicular body protein 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550410	Chmp7	charged multivesicular body protein 7	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005283	increased unsaturated fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005284	increased saturated fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005285	decreased unsaturated fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0010360	decreased liver free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0011612	increased circulating ghrelin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0011972	decreased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0013139	moribund		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0014783	decreased liver enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26479315
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:29491146
1550411	Arv1	ARV1 homolog, fatty acid homeostasis modulator	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:29491146
1550413	Rnd2	Rho family GTPase 2	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20240620	MGI			PMID:33596091
1550413	Rnd2	Rho family GTPase 2	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20210128	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20241121	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20240627	MGI			PMID:34561615
1550413	Rnd2	Rho family GTPase 2	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210128	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20240627	MGI			PMID:34561615
1550413	Rnd2	Rho family GTPase 2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20240627	MGI			PMID:34561615
1550413	Rnd2	Rho family GTPase 2	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:34561615
1550413	Rnd2	Rho family GTPase 2	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20240627	MGI			PMID:34561615
1550413	Rnd2	Rho family GTPase 2	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20221215	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0011730	increased myelin sheath thickness		IAGP		N	RGD:5509061	20240620	MGI			PMID:33596091
1550413	Rnd2	Rho family GTPase 2	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20240620	MGI			PMID:33596091
1550413	Rnd2	Rho family GTPase 2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210128	MGI			
1550413	Rnd2	Rho family GTPase 2	gene	MP:0021090	abnormal dendrite arborization pattern		IAGP		N	RGD:5509061	20240627	MGI			PMID:34561615
1550415	Slc26a11	solute carrier family 26, member 11	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20240523	MGI			
1550415	Slc26a11	solute carrier family 26, member 11	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:27390771
1550415	Slc26a11	solute carrier family 26, member 11	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20200310	MGI			PMID:27390771
1550415	Slc26a11	solute carrier family 26, member 11	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:27390771
1550415	Slc26a11	solute carrier family 26, member 11	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:27390771
1550415	Slc26a11	solute carrier family 26, member 11	gene	MP:0012007	abnormal chloride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:27390771
1550415	Slc26a11	solute carrier family 26, member 11	gene	MP:0014382	increased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:27390771
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0006051	brainstem hemorrhage		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839884
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0013806	encephalopathy		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0014180	abnormal thymus apoptosis		IAGP		N	RGD:5509061	20190314	MGI			PMID:30578322
1550418	Parl	presenilin associated, rhomboid-like	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:16839884
1550419	Dsg4	desmoglein 4	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1550419	Dsg4	desmoglein 4	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1550419	Dsg4	desmoglein 4	gene	MP:0000381	enlarged hair follicles		IEA		N	RGD:5509061	20111116	MGI			
1550419	Dsg4	desmoglein 4	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1550419	Dsg4	desmoglein 4	gene	MP:0000384	distorted hair follicle pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1550419	Dsg4	desmoglein 4	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0000580	deformed nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0000583	long toenails		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001190	reddish skin		IEA		N	RGD:5509061	20111116	MGI			
1550419	Dsg4	desmoglein 4	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1550419	Dsg4	desmoglein 4	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1550419	Dsg4	desmoglein 4	gene	MP:0001279	wavy vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0001282	short vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1550419	Dsg4	desmoglein 4	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1550419	Dsg4	desmoglein 4	gene	MP:0001786	skin edema		IEA		N	RGD:5509061	20111116	MGI			
1550419	Dsg4	desmoglein 4	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1550419	Dsg4	desmoglein 4	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0003811	abnormal hair cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0003848	brittle hair		IEA		N	RGD:5509061	20111116	MGI			
1550419	Dsg4	desmoglein 4	gene	MP:0003849	greasy coat		IEA		N	RGD:5509061	20111116	MGI			
1550419	Dsg4	desmoglein 4	gene	MP:0006365	absent guard hair		IEA		N	RGD:5509061	20111116	MGI			
1550419	Dsg4	desmoglein 4	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IEA		N	RGD:5509061	20111116	MGI			
1550419	Dsg4	desmoglein 4	gene	MP:0010688	hair follicle outer root sheath hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752833
1550419	Dsg4	desmoglein 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190418	MGI			PMID:10839719
1550419	Dsg4	desmoglein 4	gene	MP:0013115	focal hair loss in abdominal region		IEA		N	RGD:5509061	20180215	MGI			
1550419	Dsg4	desmoglein 4	gene	MP:0013116	focal hair loss in head/neck region		IEA		N	RGD:5509061	20180215	MGI			
1550419	Dsg4	desmoglein 4	gene	MP:0014659	increased skin stiffness		IAGP		N	RGD:5509061	20250508	MGI			PMID:8752833
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17170027
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0005628	decreased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0005634	decreased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17001077
1550421	Slc26a3	solute carrier family 26, member 3	gene	MP:0014483	increased feces water content		IAGP		N	RGD:5509061	20240704	MGI			PMID:17001077
1550423	Drp2	dystrophin related protein 2	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764250
1550423	Drp2	dystrophin related protein 2	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764250
1550423	Drp2	dystrophin related protein 2	gene	MP:0010050	hypermyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764250
1550423	Drp2	dystrophin related protein 2	gene	MP:0010742	increased Schwann cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764250
1550428	Crat	carnitine acetyltransferase	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0002217	small lymph nodes		IEA		N	RGD:5509061	20250508	MGI			
1550428	Crat	carnitine acetyltransferase	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550428	Crat	carnitine acetyltransferase	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560225
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20170105	MGI			
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989057
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989057
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989057
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989057
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989057
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21989057
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0014471	enhanced B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:18378701
1550432	Arhgef6	Rac/Cdc42 guanine nucleotide exchange factor 6	gene	MP:0015055	decreased synapse density		IAGP		N	RGD:5509061	20260813	MGI			PMID:21989057
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0009929	meningomyelocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550433	Ptpn9	protein tyrosine phosphatase, non-receptor type 9	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330817
1550435	Tln1	talin 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:19793892
1550435	Tln1	talin 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19793892
1550435	Tln1	talin 1	gene	MP:0002174	abnormal gastrulation movements		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18188447
1550435	Tln1	talin 1	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0003292	melena		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0003405	abnormal platelet shape		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086864
1550435	Tln1	talin 1	gene	MP:0003423	reduced thrombolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20971947
1550435	Tln1	talin 1	gene	MP:0003939	abnormal myotome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19793892
1550435	Tln1	talin 1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19793892
1550435	Tln1	talin 1	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19793892
1550435	Tln1	talin 1	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086864
1550435	Tln1	talin 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086864
1550435	Tln1	talin 1	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20971947
1550435	Tln1	talin 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086864
1550435	Tln1	talin 1	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086864
1550435	Tln1	talin 1	gene	MP:0006323	abnormal extraembryonic mesoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19793892
1550435	Tln1	talin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18086863
1550435	Tln1	talin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19793892
1550435	Tln1	talin 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IEA		N	RGD:5509061	20200310	MGI			
1550435	Tln1	talin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0011197	abnormal proamniotic cavity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0011207	absent ectoplacental cavity		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0011208	small proamniotic cavity		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0011209	absent extraembryonic coelom		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0012104	small amniotic cavity		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:11084655
1550435	Tln1	talin 1	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19793892
1550435	Tln1	talin 1	gene	MP:0030959	abnormal myoblast fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19793892
1550437	Kif5a	kinesin family member 5A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217743
1550437	Kif5a	kinesin family member 5A	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217743
1550437	Kif5a	kinesin family member 5A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217743
1550437	Kif5a	kinesin family member 5A	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217743
1550437	Kif5a	kinesin family member 5A	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1550437	Kif5a	kinesin family member 5A	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1550437	Kif5a	kinesin family member 5A	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:21335237
1550437	Kif5a	kinesin family member 5A	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217743
1550437	Kif5a	kinesin family member 5A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12682084
1550437	Kif5a	kinesin family member 5A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217743
1550437	Kif5a	kinesin family member 5A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550437	Kif5a	kinesin family member 5A	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:23217743
1550437	Kif5a	kinesin family member 5A	gene	MP:0014649	increased susceptibility to nerve crush injury		IAGP		N	RGD:5509061	20260101	MGI			PMID:37164288
1550439	Tubg1	tubulin, gamma 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1550439	Tubg1	tubulin, gamma 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15893303
1550439	Tubg1	tubulin, gamma 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15893303
1550439	Tubg1	tubulin, gamma 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15893303
1550439	Tubg1	tubulin, gamma 1	gene	MP:0020570	decreased premotor cortex size		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0020596	decreased cerebral cortex total cell area		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550439	Tubg1	tubulin, gamma 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20240418	MGI			PMID:31086189
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533944
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0002658	abnormal liver regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533944
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533944
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23975099
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533944
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0004966	abnormal inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533944
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0006205	embryonic lethality between implantation and somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0008393	absent primordial germ cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0009332	abnormal splenocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533944
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0011411	abnormal gonadal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0014619	absent spermatogonia		IAGP		N	RGD:5509061	20250213	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0014693	abnormal cell nucleus size		IAGP		N	RGD:5509061	20250710	MGI			PMID:16533944
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0014693	abnormal cell nucleus size		IAGP		N	RGD:5509061	20250710	MGI			PMID:16533945
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0014755	increased tumor cell proliferation		IAGP		N	RGD:5509061	20250904	MGI			PMID:21799785
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0030934	decreased primordial germ cell proliferation		IAGP		N	RGD:5509061	20190411	MGI			PMID:18232736
1550440	Espl1	extra spindle pole bodies 1, separase	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:18232736
1550441	Ifit3	interferon-induced protein with tetratricopeptide repeats 3	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1550441	Ifit3	interferon-induced protein with tetratricopeptide repeats 3	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20220519	MGI			
1550441	Ifit3	interferon-induced protein with tetratricopeptide repeats 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1550441	Ifit3	interferon-induced protein with tetratricopeptide repeats 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0000840	abnormal epithalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876243
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876243
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849985
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15194866
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160433
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876243
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493560
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15194866
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10357931
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876243
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001435	absent suckling reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876243
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876243
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849985
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354917
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150430	MGI			PMID:24608965
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493560
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0003637	cochlear ganglion hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493560
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0003637	cochlear ganglion hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0003684	abnormal inferior olivary complex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141225	MGI			PMID:24736625
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19323995
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876243
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876243
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15194866
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849985
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0012267	abnormal red nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8876243
1550443	Pou4f1	POU domain, class 4, transcription factor 1	gene	MP:0012268	absent red nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8955272
1550444	Gfm2	G elongation factor, mitochondrial 2	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20210128	MGI			
1550444	Gfm2	G elongation factor, mitochondrial 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550446	Vwa1	von Willebrand factor A domain containing 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19279005
1550446	Vwa1	von Willebrand factor A domain containing 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:19279005
1550446	Vwa1	von Willebrand factor A domain containing 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19279005
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210520	MGI			
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20170105	MGI			
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20241121	MGI			
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20170105	MGI			
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0010733	abnormal axon initial segment morphology		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20241121	MGI			
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0030173	abnormal orbicularis oculi muscle morphology		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550447	Tmem106b	transmembrane protein 106B	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20210408	MGI			PMID:32160553
1550452	Arhgap20	Rho GTPase activating protein 20	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20220811	MGI			
1550454	Dusp13b	dual specificity phosphatase 13B	gene	MP:0012125	decreased bronchoconstrictive response		IEA		N	RGD:5509061	20260402	MGI			
1550455	Synm	synemin, intermediate filament protein	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20160114	MGI			
1550455	Synm	synemin, intermediate filament protein	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004357	long tibia		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0009046	muscle twitch		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0010240	decreased skeletal muscle size		IAGP		N	RGD:5509061	20160310	MGI			PMID:25567810
1550455	Synm	synemin, intermediate filament protein	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20180830	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0013237	abnormal skeletal muscle regeneration		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1550455	Synm	synemin, intermediate filament protein	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231221	MGI			PMID:29247678
1550455	Synm	synemin, intermediate filament protein	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:29247678
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240627	MGI			
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0009850	embryonic lethality between implantation and placentation		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20190502	MGI			
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:29036432
1550457	Copb2	COPI coat complex subunit beta 2	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20180125	MGI			PMID:29036432
1550459	Psat1	phosphoserine aminotransferase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1550459	Psat1	phosphoserine aminotransferase 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1550459	Psat1	phosphoserine aminotransferase 1	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1550459	Psat1	phosphoserine aminotransferase 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1550459	Psat1	phosphoserine aminotransferase 1	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20160804	MGI			
1550459	Psat1	phosphoserine aminotransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23908115
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056600
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230601	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056600
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230601	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20241121	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230601	MGI			
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23908115
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606138
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779865
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779865
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779865
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056600
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056600
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779865
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23908115
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056600
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23056600
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779865
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23908115
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779865
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23908115
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20160407	MGI			PMID:23908115
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:23908115
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0030439	decreased osteoblast proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:18779865
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:23056600
1550461	Cthrc1	collagen triple helix repeat containing 1	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:23056600
1550462	Nfam1	Nfat activating molecule with ITAM motif 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220519	MGI			
1550462	Nfam1	Nfat activating molecule with ITAM motif 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1550462	Nfam1	Nfat activating molecule with ITAM motif 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20220519	MGI			
1550462	Nfam1	Nfat activating molecule with ITAM motif 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20220519	MGI			
1550462	Nfam1	Nfat activating molecule with ITAM motif 1	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20220519	MGI			
1550464	St8sia3	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20210610	MGI			PMID:31455764
1550464	St8sia3	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3	gene	MP:0013246	abnormal peptide metabolism		IAGP		N	RGD:5509061	20210610	MGI			PMID:31455764
1550465	Fzd6	frizzled class receptor 6	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169958
1550465	Fzd6	frizzled class receptor 6	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20180118	MGI			PMID:26418459
1550465	Fzd6	frizzled class receptor 6	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20231026	MGI			PMID:37622728
1550465	Fzd6	frizzled class receptor 6	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20231012	MGI			
1550465	Fzd6	frizzled class receptor 6	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20180118	MGI			PMID:26418459
1550465	Fzd6	frizzled class receptor 6	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1550465	Fzd6	frizzled class receptor 6	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550465	Fzd6	frizzled class receptor 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16495441
1550466	Ctnnb1	catenin beta 1	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0000040	decreased middle ear ossicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0000073	absent craniofacial bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1550466	Ctnnb1	catenin beta 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:19631205
1550466	Ctnnb1	catenin beta 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19631205
1550466	Ctnnb1	catenin beta 1	gene	MP:0000128	growth retardation of molars		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000128	growth retardation of molars		IAGP		N	RGD:5509061	20200310	MGI			PMID:19631205
1550466	Ctnnb1	catenin beta 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16951686
1550466	Ctnnb1	catenin beta 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15132997
1550466	Ctnnb1	catenin beta 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21924256
1550466	Ctnnb1	catenin beta 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:16936073
1550466	Ctnnb1	catenin beta 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15132997
1550466	Ctnnb1	catenin beta 1	gene	MP:0000175	absent bone marrow cell		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:18687666
1550466	Ctnnb1	catenin beta 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918954
1550466	Ctnnb1	catenin beta 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18687666
1550466	Ctnnb1	catenin beta 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0000346	broad head		IAGP		N	RGD:5509061	20200310	MGI			PMID:10932191
1550466	Ctnnb1	catenin beta 1	gene	MP:0000346	broad head		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28589954
1550466	Ctnnb1	catenin beta 1	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20200310	MGI			PMID:19154719
1550466	Ctnnb1	catenin beta 1	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20200310	MGI			PMID:19718027
1550466	Ctnnb1	catenin beta 1	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20200310	MGI			PMID:22412863
1550466	Ctnnb1	catenin beta 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0000392	accelerated hair follicle regression		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0000405	abnormal auchene hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:11371349
1550466	Ctnnb1	catenin beta 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22412863
1550466	Ctnnb1	catenin beta 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23928991
1550466	Ctnnb1	catenin beta 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:18652817
1550466	Ctnnb1	catenin beta 1	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000423	delayed hair regrowth		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23928991
1550466	Ctnnb1	catenin beta 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1550466	Ctnnb1	catenin beta 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:15132997
1550466	Ctnnb1	catenin beta 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:15371327
1550466	Ctnnb1	catenin beta 1	gene	MP:0000447	flattened snout		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23873040
1550466	Ctnnb1	catenin beta 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15131783
1550466	Ctnnb1	catenin beta 1	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15131783
1550466	Ctnnb1	catenin beta 1	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18536716
1550466	Ctnnb1	catenin beta 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21205788
1550466	Ctnnb1	catenin beta 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:20454682
1550466	Ctnnb1	catenin beta 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:20454682
1550466	Ctnnb1	catenin beta 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22792366
1550466	Ctnnb1	catenin beta 1	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:22792366
1550466	Ctnnb1	catenin beta 1	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23928991
1550466	Ctnnb1	catenin beta 1	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20818428
1550466	Ctnnb1	catenin beta 1	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368895
1550466	Ctnnb1	catenin beta 1	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21504907
1550466	Ctnnb1	catenin beta 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:15132997
1550466	Ctnnb1	catenin beta 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:15371327
1550466	Ctnnb1	catenin beta 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12569130
1550466	Ctnnb1	catenin beta 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18423204
1550466	Ctnnb1	catenin beta 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20152185
1550466	Ctnnb1	catenin beta 1	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20152185
1550466	Ctnnb1	catenin beta 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20200310	MGI			PMID:12569130
1550466	Ctnnb1	catenin beta 1	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20200310	MGI			PMID:18423204
1550466	Ctnnb1	catenin beta 1	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24290754
1550466	Ctnnb1	catenin beta 1	gene	MP:0000653	abnormal sex gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000674	abnormal sweat gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17652354
1550466	Ctnnb1	catenin beta 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28589954
1550466	Ctnnb1	catenin beta 1	gene	MP:0000763	abnormal filiform papillae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28589954
1550466	Ctnnb1	catenin beta 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12798297
1550466	Ctnnb1	catenin beta 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0000906	abnormal trigeminal V mesencephalic nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20200310	MGI			PMID:22007134
1550466	Ctnnb1	catenin beta 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12798297
1550466	Ctnnb1	catenin beta 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0001062	absent oculomotor nerve		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:19237610
1550466	Ctnnb1	catenin beta 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19686689
1550466	Ctnnb1	catenin beta 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23873040
1550466	Ctnnb1	catenin beta 1	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20200310	MGI			PMID:19686689
1550466	Ctnnb1	catenin beta 1	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20200310	MGI			PMID:23873040
1550466	Ctnnb1	catenin beta 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19718027
1550466	Ctnnb1	catenin beta 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17222338
1550466	Ctnnb1	catenin beta 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:18687666
1550466	Ctnnb1	catenin beta 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:19237610
1550466	Ctnnb1	catenin beta 1	gene	MP:0001280	loss of vibrissae		IAGP		N	RGD:5509061	20200310	MGI			PMID:18652817
1550466	Ctnnb1	catenin beta 1	gene	MP:0001283	sparse vibrissae		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22007134
1550466	Ctnnb1	catenin beta 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18652817
1550466	Ctnnb1	catenin beta 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19570848
1550466	Ctnnb1	catenin beta 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22007134
1550466	Ctnnb1	catenin beta 1	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20200310	MGI			PMID:10932191
1550466	Ctnnb1	catenin beta 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20200310	MGI			PMID:18652817
1550466	Ctnnb1	catenin beta 1	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:12569130
1550466	Ctnnb1	catenin beta 1	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18687666
1550466	Ctnnb1	catenin beta 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18463637
1550466	Ctnnb1	catenin beta 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19023080
1550466	Ctnnb1	catenin beta 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20200310	MGI			PMID:8582267
1550466	Ctnnb1	catenin beta 1	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12569130
1550466	Ctnnb1	catenin beta 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18781635
1550466	Ctnnb1	catenin beta 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0001684	abnormal axial mesoderm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23638095
1550466	Ctnnb1	catenin beta 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23638095
1550466	Ctnnb1	catenin beta 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:8582267
1550466	Ctnnb1	catenin beta 1	gene	MP:0001705	abnormal proximal-distal axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0001710	absent amniotic folds		IAGP		N	RGD:5509061	20200310	MGI			PMID:8582267
1550466	Ctnnb1	catenin beta 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17222338
1550466	Ctnnb1	catenin beta 1	gene	MP:0001884	mammary gland alveolar hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24290754
1550466	Ctnnb1	catenin beta 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:19023080
1550466	Ctnnb1	catenin beta 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17222338
1550466	Ctnnb1	catenin beta 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22792366
1550466	Ctnnb1	catenin beta 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20084116
1550466	Ctnnb1	catenin beta 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:19631205
1550466	Ctnnb1	catenin beta 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:22792366
1550466	Ctnnb1	catenin beta 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20200310	MGI			PMID:11371349
1550466	Ctnnb1	catenin beta 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:27134165
1550466	Ctnnb1	catenin beta 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:22792366
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:10545105
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:16951686
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17222338
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18463637
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18536716
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18687666
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19092805
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20818428
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368895
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21504907
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23928991
1550466	Ctnnb1	catenin beta 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8582267
1550466	Ctnnb1	catenin beta 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15132997
1550466	Ctnnb1	catenin beta 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18463637
1550466	Ctnnb1	catenin beta 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15729346
1550466	Ctnnb1	catenin beta 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12798297
1550466	Ctnnb1	catenin beta 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1550466	Ctnnb1	catenin beta 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:10545105
1550466	Ctnnb1	catenin beta 1	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0002210	abnormal sex determination		IAGP		N	RGD:5509061	20200310	MGI			PMID:21490063
1550466	Ctnnb1	catenin beta 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28196692
1550466	Ctnnb1	catenin beta 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1550466	Ctnnb1	catenin beta 1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002351	abnormal cervical lymph node morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:10545105
1550466	Ctnnb1	catenin beta 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18536716
1550466	Ctnnb1	catenin beta 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21205788
1550466	Ctnnb1	catenin beta 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0002579	disorganized secondary lens fibers		IAGP		N	RGD:5509061	20200310	MGI			PMID:18652817
1550466	Ctnnb1	catenin beta 1	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17222338
1550466	Ctnnb1	catenin beta 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20200310	MGI			PMID:19543268
1550466	Ctnnb1	catenin beta 1	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0002726	abnormal pulmonary vein morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23873040
1550466	Ctnnb1	catenin beta 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0002768	small adrenal glands		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19154719
1550466	Ctnnb1	catenin beta 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0002809	increased spinal cord size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12798297
1550466	Ctnnb1	catenin beta 1	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21262216
1550466	Ctnnb1	catenin beta 1	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21924256
1550466	Ctnnb1	catenin beta 1	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20010698
1550466	Ctnnb1	catenin beta 1	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19092805
1550466	Ctnnb1	catenin beta 1	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:8582267
1550466	Ctnnb1	catenin beta 1	gene	MP:0003126	abnormal external female genitalia morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19282366
1550466	Ctnnb1	catenin beta 1	gene	MP:0003129	persistent cloaca		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0003153	early eyelid opening		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0003190	fused synovial joints		IAGP		N	RGD:5509061	20200310	MGI			PMID:15371327
1550466	Ctnnb1	catenin beta 1	gene	MP:0003190	fused synovial joints		IAGP		N	RGD:5509061	20200310	MGI			PMID:16936073
1550466	Ctnnb1	catenin beta 1	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22007134
1550466	Ctnnb1	catenin beta 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18652817
1550466	Ctnnb1	catenin beta 1	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18652817
1550466	Ctnnb1	catenin beta 1	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19570848
1550466	Ctnnb1	catenin beta 1	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20200310	MGI			PMID:19686689
1550466	Ctnnb1	catenin beta 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20084116
1550466	Ctnnb1	catenin beta 1	gene	MP:0003334	pancreas fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17222338
1550466	Ctnnb1	catenin beta 1	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0003417	premature endochondral bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:16936073
1550466	Ctnnb1	catenin beta 1	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22792366
1550466	Ctnnb1	catenin beta 1	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0003553	abnormal foreskin morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19282366
1550466	Ctnnb1	catenin beta 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:20454682
1550466	Ctnnb1	catenin beta 1	gene	MP:0003605	fused kidneys		IAGP		N	RGD:5509061	20200310	MGI			PMID:22792366
1550466	Ctnnb1	catenin beta 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12798297
1550466	Ctnnb1	catenin beta 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:19543268
1550466	Ctnnb1	catenin beta 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:22792366
1550466	Ctnnb1	catenin beta 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22377357
1550466	Ctnnb1	catenin beta 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1550466	Ctnnb1	catenin beta 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866165
1550466	Ctnnb1	catenin beta 1	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20200310	MGI			PMID:21924256
1550466	Ctnnb1	catenin beta 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0003826	abnormal Mullerian duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21490063
1550466	Ctnnb1	catenin beta 1	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20200310	MGI			PMID:21924256
1550466	Ctnnb1	catenin beta 1	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8582267
1550466	Ctnnb1	catenin beta 1	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0003895	increased ectoderm apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12569130
1550466	Ctnnb1	catenin beta 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0003936	abnormal reproductive system development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18781635
1550466	Ctnnb1	catenin beta 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23873040
1550466	Ctnnb1	catenin beta 1	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866165
1550466	Ctnnb1	catenin beta 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23638095
1550466	Ctnnb1	catenin beta 1	gene	MP:0004081	abnormal globus pallidus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16678101
1550466	Ctnnb1	catenin beta 1	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24094324
1550466	Ctnnb1	catenin beta 1	gene	MP:0004205	absent hyoid bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23736260
1550466	Ctnnb1	catenin beta 1	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20200310	MGI			PMID:21924256
1550466	Ctnnb1	catenin beta 1	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20200310	MGI			PMID:12569130
1550466	Ctnnb1	catenin beta 1	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0004382	abnormal hair follicle melanogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862558
1550466	Ctnnb1	catenin beta 1	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:15870116
1550466	Ctnnb1	catenin beta 1	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:16738313
1550466	Ctnnb1	catenin beta 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1550466	Ctnnb1	catenin beta 1	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0004572	fusion of basioccipital and basisphenoid bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:15132997
1550466	Ctnnb1	catenin beta 1	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0004791	absent lower incisors		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866165
1550466	Ctnnb1	catenin beta 1	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0004830	short incisors		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:28196692
1550466	Ctnnb1	catenin beta 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866165
1550466	Ctnnb1	catenin beta 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866165
1550466	Ctnnb1	catenin beta 1	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0005077	abnormal melanogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22377357
1550466	Ctnnb1	catenin beta 1	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12569130
1550466	Ctnnb1	catenin beta 1	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368895
1550466	Ctnnb1	catenin beta 1	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20200310	MGI			PMID:19023080
1550466	Ctnnb1	catenin beta 1	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862558
1550466	Ctnnb1	catenin beta 1	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17222338
1550466	Ctnnb1	catenin beta 1	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16256739
1550466	Ctnnb1	catenin beta 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12798297
1550466	Ctnnb1	catenin beta 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12569130
1550466	Ctnnb1	catenin beta 1	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0005315	absent pituitary gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:16678101
1550466	Ctnnb1	catenin beta 1	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20200310	MGI			PMID:19631205
1550466	Ctnnb1	catenin beta 1	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22377357
1550466	Ctnnb1	catenin beta 1	gene	MP:0005504	abnormal ligament morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22377357
1550466	Ctnnb1	catenin beta 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21571217
1550466	Ctnnb1	catenin beta 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21924256
1550466	Ctnnb1	catenin beta 1	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1550466	Ctnnb1	catenin beta 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866165
1550466	Ctnnb1	catenin beta 1	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:19023080
1550466	Ctnnb1	catenin beta 1	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0006236	absent Meibomian glands		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20260716	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19237610
1550466	Ctnnb1	catenin beta 1	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24290754
1550466	Ctnnb1	catenin beta 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:20152185
1550466	Ctnnb1	catenin beta 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22377357
1550466	Ctnnb1	catenin beta 1	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22722829
1550466	Ctnnb1	catenin beta 1	gene	MP:0006292	abnormal nasal placode morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0006305	abnormal optic eminence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16936073
1550466	Ctnnb1	catenin beta 1	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18687666
1550466	Ctnnb1	catenin beta 1	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20200310	MGI			PMID:20084116
1550466	Ctnnb1	catenin beta 1	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20200310	MGI			PMID:23202126
1550466	Ctnnb1	catenin beta 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21504907
1550466	Ctnnb1	catenin beta 1	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0008154	decreased diameter of humerus		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0008264	absent hippocampus CA1 region		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0008266	absent hippocampus CA2 region		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0008268	absent hippocampus CA3 region		IAGP		N	RGD:5509061	20200310	MGI			PMID:15219872
1550466	Ctnnb1	catenin beta 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0008274	failure of bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:16936073
1550466	Ctnnb1	catenin beta 1	gene	MP:0008274	failure of bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:21924256
1550466	Ctnnb1	catenin beta 1	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16678101
1550466	Ctnnb1	catenin beta 1	gene	MP:0008330	absent somatotrophs		IAGP		N	RGD:5509061	20200310	MGI			PMID:16678101
1550466	Ctnnb1	catenin beta 1	gene	MP:0008333	absent lactotrophs		IAGP		N	RGD:5509061	20200310	MGI			PMID:16678101
1550466	Ctnnb1	catenin beta 1	gene	MP:0008335	decreased gonadotroph cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:16678101
1550466	Ctnnb1	catenin beta 1	gene	MP:0008339	absent thyrotrophs		IAGP		N	RGD:5509061	20200310	MGI			PMID:16678101
1550466	Ctnnb1	catenin beta 1	gene	MP:0008340	increased corticotroph cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:16678101
1550466	Ctnnb1	catenin beta 1	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918954
1550466	Ctnnb1	catenin beta 1	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0008464	absent peripheral lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0008732	reduced hair shaft melanin granule number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862558
1550466	Ctnnb1	catenin beta 1	gene	MP:0008794	increased lens epithelium apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19570848
1550466	Ctnnb1	catenin beta 1	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20200310	MGI			PMID:18652817
1550466	Ctnnb1	catenin beta 1	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0008860	abnormal hair cycle telogen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0009109	decreased pancreas weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17222338
1550466	Ctnnb1	catenin beta 1	gene	MP:0009139	failure of Mullerian duct regression		IAGP		N	RGD:5509061	20200310	MGI			PMID:21490063
1550466	Ctnnb1	catenin beta 1	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0009154	pancreatic acinar hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17222338
1550466	Ctnnb1	catenin beta 1	gene	MP:0009199	abnormal external male genitalia morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19282366
1550466	Ctnnb1	catenin beta 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550466	Ctnnb1	catenin beta 1	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20210311	MGI			PMID:31819003
1550466	Ctnnb1	catenin beta 1	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550466	Ctnnb1	catenin beta 1	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20210311	MGI			PMID:31819003
1550466	Ctnnb1	catenin beta 1	gene	MP:0009272	decreased guard hair length		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0009388	abnormal epidermal melanocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27134165
1550466	Ctnnb1	catenin beta 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0009545	abnormal dermis papillary layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20818428
1550466	Ctnnb1	catenin beta 1	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368895
1550466	Ctnnb1	catenin beta 1	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23928991
1550466	Ctnnb1	catenin beta 1	gene	MP:0009612	thick epidermis suprabasal layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0009629	small brachial lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0009632	small axillary lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0009684	abnormal spinal cord lateral motor column morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0009685	abnormal spinal cord motor column morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0009686	abnormal spinal cord medial motor column morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0009715	thick epidermis stratum basale		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1550466	Ctnnb1	catenin beta 1	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862558
1550466	Ctnnb1	catenin beta 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:19631205
1550466	Ctnnb1	catenin beta 1	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0009928	abnormal pinna hair pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862558
1550466	Ctnnb1	catenin beta 1	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16951686
1550466	Ctnnb1	catenin beta 1	gene	MP:0009933	abnormal tail hair pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862558
1550466	Ctnnb1	catenin beta 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0010054	increased hepatoblastoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16951686
1550466	Ctnnb1	catenin beta 1	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21205788
1550466	Ctnnb1	catenin beta 1	gene	MP:0010234	abnormal vibrissa follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:18652817
1550466	Ctnnb1	catenin beta 1	gene	MP:0010275	increased melanoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:20048081
1550466	Ctnnb1	catenin beta 1	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0010313	increased osteoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866165
1550466	Ctnnb1	catenin beta 1	gene	MP:0010318	increased salivary gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23736260
1550466	Ctnnb1	catenin beta 1	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24094324
1550466	Ctnnb1	catenin beta 1	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550466	Ctnnb1	catenin beta 1	gene	MP:0010682	abnormal hair follicle infundibulum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0010741	abnormal melanocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:27134165
1550466	Ctnnb1	catenin beta 1	gene	MP:0010864	abnormal enamel knot morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19631205
1550466	Ctnnb1	catenin beta 1	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0010907	absent lung buds		IAGP		N	RGD:5509061	20200310	MGI			PMID:19686689
1550466	Ctnnb1	catenin beta 1	gene	MP:0010939	abnormal mandibular prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0010939	abnormal mandibular prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0010964	increased compact bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866165
1550466	Ctnnb1	catenin beta 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19543268
1550466	Ctnnb1	catenin beta 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12569130
1550466	Ctnnb1	catenin beta 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15371327
1550466	Ctnnb1	catenin beta 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19718027
1550466	Ctnnb1	catenin beta 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18463637
1550466	Ctnnb1	catenin beta 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20084116
1550466	Ctnnb1	catenin beta 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19023080
1550466	Ctnnb1	catenin beta 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:8582267
1550466	Ctnnb1	catenin beta 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18781635
1550466	Ctnnb1	catenin beta 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21876000
1550466	Ctnnb1	catenin beta 1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18250098
1550466	Ctnnb1	catenin beta 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15132997
1550466	Ctnnb1	catenin beta 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0011194	abnormal hair follicle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20412777
1550466	Ctnnb1	catenin beta 1	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24315444
1550466	Ctnnb1	catenin beta 1	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0011298	ureter hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22792366
1550466	Ctnnb1	catenin beta 1	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0011407	absent nephrogenic zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0011496	abnormal head size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228006
1550466	Ctnnb1	catenin beta 1	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0011712	arrested osteoblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854976
1550466	Ctnnb1	catenin beta 1	gene	MP:0011712	arrested osteoblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16936073
1550466	Ctnnb1	catenin beta 1	gene	MP:0011712	arrested osteoblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21924256
1550466	Ctnnb1	catenin beta 1	gene	MP:0011846	decreased kidney collecting duct number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18358465
1550466	Ctnnb1	catenin beta 1	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0012110	increased hair follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23736260
1550466	Ctnnb1	catenin beta 1	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0012141	absent hindbrain		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190459
1550466	Ctnnb1	catenin beta 1	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0012163	abnormal dental mesenchyme morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19631205
1550466	Ctnnb1	catenin beta 1	gene	MP:0012300	abnormal umbilical cord blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12975353
1550466	Ctnnb1	catenin beta 1	gene	MP:0012306	enhanced spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0012318	slow extinction of fear memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19237610
1550466	Ctnnb1	catenin beta 1	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0012467	increased striatum size		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0012516	absent metencephalon		IAGP		N	RGD:5509061	20200310	MGI			PMID:11262227
1550466	Ctnnb1	catenin beta 1	gene	MP:0012568	decreased mammary gland tumor incidence in breeding females		IAGP		N	RGD:5509061	20200310	MGI			PMID:24290754
1550466	Ctnnb1	catenin beta 1	gene	MP:0012570	increased mammary gland tumor incidence in breeding females		IAGP		N	RGD:5509061	20200310	MGI			PMID:24290754
1550466	Ctnnb1	catenin beta 1	gene	MP:0012571	increased mammary gland tumor incidence in virgin females		IAGP		N	RGD:5509061	20200310	MGI			PMID:24290754
1550466	Ctnnb1	catenin beta 1	gene	MP:0012739	abnormal anterior primitive streak morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18781635
1550466	Ctnnb1	catenin beta 1	gene	MP:0013180	truncated tail bud		IAGP		N	RGD:5509061	20200310	MGI			PMID:22991437
1550466	Ctnnb1	catenin beta 1	gene	MP:0013445	Harderian gland atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0013466	keratoconjunctivitis sicca		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15131783
1550466	Ctnnb1	catenin beta 1	gene	MP:0013733	squamous metaplasia of bulbourethral gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550466	Ctnnb1	catenin beta 1	gene	MP:0013734	squamous metaplasia of preputial gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550466	Ctnnb1	catenin beta 1	gene	MP:0013735	squamous metaplasia of urethral gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:19117991
1550466	Ctnnb1	catenin beta 1	gene	MP:0013745	abnormal eyelid margin morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0013945	abnormal elbow joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16936073
1550466	Ctnnb1	catenin beta 1	gene	MP:0014077	ectopic Paneth cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:15131783
1550466	Ctnnb1	catenin beta 1	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16936073
1550466	Ctnnb1	catenin beta 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23736260
1550466	Ctnnb1	catenin beta 1	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:28196692
1550466	Ctnnb1	catenin beta 1	gene	MP:0015003	decreased embryo length		IAGP		N	RGD:5509061	20260611	MGI			PMID:10662781
1550466	Ctnnb1	catenin beta 1	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:16936073
1550466	Ctnnb1	catenin beta 1	gene	MP:0020288	ectopic limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:23358455
1550466	Ctnnb1	catenin beta 1	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20200310	MGI			PMID:27131348
1550466	Ctnnb1	catenin beta 1	gene	MP:0020526	enlarged thalamus		IAGP		N	RGD:5509061	20200310	MGI			PMID:24614104
1550466	Ctnnb1	catenin beta 1	gene	MP:0021103	abnormal ventral interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:22036570
1550466	Ctnnb1	catenin beta 1	gene	MP:0030252	narrow frontonasal prominence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0030302	abnormal maxillary zygomatic process morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21087601
1550466	Ctnnb1	catenin beta 1	gene	MP:0030324	abnormal anterior head development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21307168
1550466	Ctnnb1	catenin beta 1	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20200310	MGI			PMID:11585809
1550466	Ctnnb1	catenin beta 1	gene	MP:0030906	decreased melanoblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862558
1550466	Ctnnb1	catenin beta 1	gene	MP:0030908	abnormal melanocyte differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:27134165
1550466	Ctnnb1	catenin beta 1	gene	MP:0031016	decreased granulosa cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0031019	increased granulosa cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21860425
1550466	Ctnnb1	catenin beta 1	gene	MP:0031080	pulmonary embolism		IAGP		N	RGD:5509061	20200709	MGI			PMID:18687666
1550466	Ctnnb1	catenin beta 1	gene	MP:0031395	cutaneous mastocytosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:24315444
1550468	Cep97	centrosomal protein 97	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20241121	MGI			
1550468	Cep97	centrosomal protein 97	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20241121	MGI			
1550468	Cep97	centrosomal protein 97	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1550468	Cep97	centrosomal protein 97	gene	MP:0001785	edema		IEA		N	RGD:5509061	20241121	MGI			
1550468	Cep97	centrosomal protein 97	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1550468	Cep97	centrosomal protein 97	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1550468	Cep97	centrosomal protein 97	gene	MP:0008854	bleb		IEA		N	RGD:5509061	20210520	MGI			
1550468	Cep97	centrosomal protein 97	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001697	abnormal embryo size		IAGP		N	RGD:5509061	20230629	MGI			PMID:36449618
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20230629	MGI			PMID:36449618
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0003773	eclabion		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004055	heart atrium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0005385	cardiovascular system phenotype		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0006411	upturned snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0006411	upturned snout		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0008957	abnormal placenta junctional zone morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0008958	abnormal trophoblast glycogen cell morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0008959	abnormal spongiotrophoblast cell morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0009777	abnormal behavioral response to anesthetic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0010038	abnormal placenta physiology		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0010405	ostium secundum atrial septal defect		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20230629	MGI			PMID:36449618
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:27606604
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0011262	abnormal pharyngeal arch mesenchyme morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:19763162
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0012523	abnormal upper lip morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20151224	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0030065	face hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:24700590
1550472	Nipbl	NIPBL cohesin loading factor	gene	MP:0030303	small ethmoid bone		IAGP		N	RGD:5509061	20171109	MGI			PMID:19763162
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20200514	MGI			
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20201022	MGI			
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0005141	liver hyperplasia		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20160407	MGI			PMID:25088416
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0014253	decreased paired-pulse ratio		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0014345	abnormal neuron mitochondrial morphology		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0020510	increased dendritic spine length		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0020511	decreased dendritic spine length		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550473	Trap1	TNF receptor-associated protein 1	gene	MP:0021009	abnormal synaptic physiology		IAGP		N	RGD:5509061	20250410	MGI			PMID:39333440
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9614081
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210826	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20170223	MGI			PMID:24019477
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20170223	MGI			PMID:24019477
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0000646	enlarged adrenocortical cells		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20210826	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9614081
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:9614081
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210826	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20170105	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20210826	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210826	MGI			
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20170223	MGI			PMID:24019477
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0012226	increased sterol level		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0012337	increased vitamin D level		IAGP		N	RGD:5509061	20240704	MGI			PMID:9614081
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0012338	decreased bile salt level		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0013307	increased adrenal gland weight		IAGP		N	RGD:5509061	20170302	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0014476	abnormal feces lipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0014479	decreased feces bile salt level		IAGP		N	RGD:5509061	20240704	MGI			PMID:11001949
1550475	Cyp27a1	cytochrome P450, family 27, subfamily a, polypeptide 1	gene	MP:0031631	decreased lung cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:11001949
1550476	Neurog1	neurogenin 1	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640277
1550476	Neurog1	neurogenin 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11825874
1550476	Neurog1	neurogenin 1	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539122
1550476	Neurog1	neurogenin 1	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539122
1550476	Neurog1	neurogenin 1	gene	MP:0001075	abnormal accessory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539122
1550476	Neurog1	neurogenin 1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539122
1550476	Neurog1	neurogenin 1	gene	MP:0001097	abnormal superior glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539122
1550476	Neurog1	neurogenin 1	gene	MP:0001101	abnormal superior vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539122
1550476	Neurog1	neurogenin 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539122
1550476	Neurog1	neurogenin 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640277
1550476	Neurog1	neurogenin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539122
1550476	Neurog1	neurogenin 1	gene	MP:0013183	absent trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9539122
1550477	Cpsf1	cleavage and polyadenylation specific factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:21220323
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:9050846
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:9050846
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:21220323
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001396	unidirectional circling		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20210415	MGI			PMID:31907305
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20210415	MGI			PMID:31907305
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20210415	MGI			PMID:31907305
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001499	abnormal kindling response		IAGP		N	RGD:5509061	20200310	MGI			PMID:24700286
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20200310	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20200310	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21220323
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:24700286
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:9050846
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20210415	MGI			PMID:31907305
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:21220323
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20200310	MGI			PMID:9050846
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201231	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21220323
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0003956	abnormal body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12077185
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9050846
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:31653840
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21220323
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005407	hyperalgesia		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12077185
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21220323
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21220323
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20200310	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20201022	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20200310	MGI			PMID:19225179
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20210128	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20200310	MGI			PMID:20622165
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20200310	MGI			PMID:21220323
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24700286
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24700286
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9050846
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9050846
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9501252
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19225179
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0011678	abnormal vomeronasal sensory neuron physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31653840
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20210415	MGI			PMID:31907305
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20200310	MGI			
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0014620	abnormal interictal brain wave pattern		IAGP		N	RGD:5509061	20251204	MGI			PMID:24700286
1550478	Gnao1	guanine nucleotide binding protein, alpha O	gene	MP:0020424	increased kindling response		IAGP		N	RGD:5509061	20200310	MGI			PMID:30682176
1550484	Krt10	keratin 10	gene	MP:0000020	scaly ears		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0000410	waved hair		IEA		N	RGD:5509061	20111116	MGI			
1550484	Krt10	keratin 10	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550484	Krt10	keratin 10	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550484	Krt10	keratin 10	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:11157989
1550484	Krt10	keratin 10	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:24751727
1550484	Krt10	keratin 10	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20180719	MGI			PMID:11157989
1550484	Krt10	keratin 10	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20180719	MGI			PMID:11157989
1550484	Krt10	keratin 10	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11408568
1550484	Krt10	keratin 10	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15482487
1550484	Krt10	keratin 10	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:22375063
1550484	Krt10	keratin 10	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:24751727
1550484	Krt10	keratin 10	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15482487
1550484	Krt10	keratin 10	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:22375063
1550484	Krt10	keratin 10	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:24751727
1550484	Krt10	keratin 10	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11157989
1550484	Krt10	keratin 10	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11408568
1550484	Krt10	keratin 10	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11408568
1550484	Krt10	keratin 10	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550484	Krt10	keratin 10	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11157989
1550484	Krt10	keratin 10	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:22375063
1550484	Krt10	keratin 10	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:24751727
1550484	Krt10	keratin 10	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20180719	MGI			PMID:15482487
1550484	Krt10	keratin 10	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550484	Krt10	keratin 10	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20180719	MGI			PMID:22375063
1550484	Krt10	keratin 10	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550484	Krt10	keratin 10	gene	MP:0009594	abnormal corneocyte envelope morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:22375063
1550484	Krt10	keratin 10	gene	MP:0009596	abnormal stratum corneum lipid matrix formation		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550484	Krt10	keratin 10	gene	MP:0009600	hypergranulosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:24751727
1550484	Krt10	keratin 10	gene	MP:0009606	increased keratohyalin granule size		IAGP		N	RGD:5509061	20180719	MGI			PMID:11408568
1550484	Krt10	keratin 10	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:11157989
1550484	Krt10	keratin 10	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:22375063
1550484	Krt10	keratin 10	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:8603923
1550484	Krt10	keratin 10	gene	MP:0013373	increased sebum secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550484	Krt10	keratin 10	gene	MP:0013375	abnormal sebocyte morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550484	Krt10	keratin 10	gene	MP:0013376	abnormal sebocyte differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550484	Krt10	keratin 10	gene	MP:0014056	increased sebocyte proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:15679119
1550485	Iigp1	interferon inducible GTPase 1	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:16304607
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20170105	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9382868
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20170105	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9382868
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11150240
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9382868
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9382868
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20170105	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9382868
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20170105	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0003870	decreased urine glucose level		IEA		N	RGD:5509061	20211021	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:9382868
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20181227	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9585413
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:9382868
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20170105	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0011436	decreased urine magnesium level		IEA		N	RGD:5509061	20211021	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0011471	decreased urine creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9382868
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9382868
1550486	Myh1	myosin, heavy polypeptide 1, skeletal muscle, adult	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050047
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17671657
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050047
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050047
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050047
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0003357	impaired granulosa cell differentiation		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0003657	abnormal erythrocyte osmotic lysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050047
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050047
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050047
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050047
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17671657
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0006038	increased mitochondrial fission		IAGP		N	RGD:5509061	20141003	MGI			PMID:21124450
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050047
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0011124	increased primary ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0011385	abnormal testosterone level		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0014514	increased circulating anti-Mullerian hormone level		IAGP		N	RGD:5509061	20240822	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0021106	abnormal secondary ovarian follicle morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0031383	increased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:35459945
1550489	Prkaa1	protein kinase, AMP-activated, alpha 1 catalytic subunit	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:14573616
1550491	Cbx7	chromobox 7	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214847
1550491	Cbx7	chromobox 7	gene	MP:0012725	small sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1550492	Trim54	tripartite motif-containing 54	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360532
1550492	Trim54	tripartite motif-containing 54	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231221	MGI			PMID:17360532
1550494	Imp3	IMP3, U3 small nucleolar ribonucleoprotein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20251127	MGI			PMID:33297405
1550494	Imp3	IMP3, U3 small nucleolar ribonucleoprotein	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20251127	MGI			PMID:33297405
1550494	Imp3	IMP3, U3 small nucleolar ribonucleoprotein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20251127	MGI			PMID:33297405
1550494	Imp3	IMP3, U3 small nucleolar ribonucleoprotein	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20251127	MGI			PMID:33297405
1550494	Imp3	IMP3, U3 small nucleolar ribonucleoprotein	gene	MP:0008989	abnormal liver sinusoid morphology		IAGP		N	RGD:5509061	20251127	MGI			PMID:33297405
1550496	Adam28	a disintegrin and metallopeptidase domain 28	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20210114	MGI			PMID:30647853
1550496	Adam28	a disintegrin and metallopeptidase domain 28	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20210114	MGI			PMID:30647853
1550496	Adam28	a disintegrin and metallopeptidase domain 28	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210114	MGI			PMID:30647853
1550496	Adam28	a disintegrin and metallopeptidase domain 28	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210114	MGI			PMID:30647853
1550496	Adam28	a disintegrin and metallopeptidase domain 28	gene	MP:0012762	abnormal alpha-beta T cell morphology		IAGP		N	RGD:5509061	20210114	MGI			PMID:30647853
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20230601	MGI			
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20230601	MGI			
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20230601	MGI			
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20230601	MGI			
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20240523	MGI			
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20230601	MGI			
1550498	Brinp3	bone morphogenetic protein/retinoic acid inducible neural specific 3	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20191024	MGI			PMID:30733438
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20191024	MGI			PMID:30733438
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20191024	MGI			PMID:30733438
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0004958	enlarged prostate gland		IAGP		N	RGD:5509061	20191024	MGI			PMID:30733438
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20191024	MGI			PMID:30733438
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0009220	increased prostate gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20191024	MGI			PMID:30733438
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20191024	MGI			PMID:30733438
1550499	Usp11	ubiquitin specific peptidase 11	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20191024	MGI			PMID:30733438
1550503	Angpt2	angiopoietin 2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1550503	Angpt2	angiopoietin 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1550503	Angpt2	angiopoietin 2	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20210128	MGI			
1550503	Angpt2	angiopoietin 2	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20210128	MGI			
1550503	Angpt2	angiopoietin 2	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1550503	Angpt2	angiopoietin 2	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0004226	absent Schlemm's canal		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0005257	abnormal intraocular pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20230810	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0006149	decreased visual acuity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550503	Angpt2	angiopoietin 2	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0012684	abnormal pleural cavity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12361603
1550503	Angpt2	angiopoietin 2	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:25202984
1550503	Angpt2	angiopoietin 2	gene	MP:0031500	increased cornea size		IAGP		N	RGD:5509061	20230810	MGI			PMID:25202984
1550506	Wdr59	WD repeat domain 59	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1550506	Wdr59	WD repeat domain 59	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20200402	MGI			
1550506	Wdr59	WD repeat domain 59	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200310	MGI			
1550506	Wdr59	WD repeat domain 59	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20210826	MGI			
1550506	Wdr59	WD repeat domain 59	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1550506	Wdr59	WD repeat domain 59	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1550506	Wdr59	WD repeat domain 59	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1550506	Wdr59	WD repeat domain 59	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550506	Wdr59	WD repeat domain 59	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0005633	increased circulating sodium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:16923965
1550507	Hspa4l	heat shock protein 4 like	gene	MP:0014686	premature spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:16923965
1550508	Pkp2	plakophilin 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0005435	hemoperitoneum		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550508	Pkp2	plakophilin 2	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15479741
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001195	flaky skin		IEA		N	RGD:5509061	20200310	MGI			
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20200310	MGI			PMID:15466487
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15590704
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001230	epidermal desquamation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001230	epidermal desquamation		IAGP		N	RGD:5509061	20200806	MGI			PMID:31255470
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15466487
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15466487
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20703245
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31255470
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15590704
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001280	loss of vibrissae		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001283	sparse vibrissae		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20240523	MGI			
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20200310	MGI			PMID:15466487
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20200310	MGI			PMID:15590704
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20703245
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20703245
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20200806	MGI			PMID:31255470
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20703245
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31255470
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20703245
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:31255470
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20200310	MGI			PMID:15466487
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20200310	MGI			PMID:15590704
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20200806	MGI			PMID:31255470
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20200806	MGI			PMID:31255470
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0009594	abnormal corneocyte envelope morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15590704
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0010234	abnormal vibrissa follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15466487
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15590704
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15619623
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20703245
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200806	MGI			PMID:31255470
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0014431	increased chemokine level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0014448	increased enzyme/coenzyme level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550511	Spink5	serine peptidase inhibitor, Kazal type 5	gene	MP:0020254	decreased collagen level		IAGP		N	RGD:5509061	20250626	MGI			PMID:38316920
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20170105	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1550512	Isca1	iron-sulfur cluster assembly 1	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1550513	Fbxl22	F-box and leucine-rich repeat protein 22	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20200310	MGI			
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109567
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109567
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:16914726
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109567
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109567
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727190
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727190
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109567
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:16914726
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727190
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727190
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727190
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:16914726
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727190
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:16914726
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727190
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109567
1550514	Vtcn1	V-set domain containing T cell activation inhibitor 1	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727190
1550515	Slc16a13	solute carrier family 16 (monocarboxylic acid transporters), member 13	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20211209	MGI			PMID:34211098
1550515	Slc16a13	solute carrier family 16 (monocarboxylic acid transporters), member 13	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20211209	MGI			PMID:34211098
1550515	Slc16a13	solute carrier family 16 (monocarboxylic acid transporters), member 13	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20211209	MGI			PMID:34211098
1550515	Slc16a13	solute carrier family 16 (monocarboxylic acid transporters), member 13	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20211209	MGI			PMID:34211098
1550515	Slc16a13	solute carrier family 16 (monocarboxylic acid transporters), member 13	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20211209	MGI			PMID:34211098
1550515	Slc16a13	solute carrier family 16 (monocarboxylic acid transporters), member 13	gene	MP:0014909	increased hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:34211098
1550515	Slc16a13	solute carrier family 16 (monocarboxylic acid transporters), member 13	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20211209	MGI			PMID:34211098
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0003415	priapism		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550516	Scyl2	SCY1-like 2 (S. cerevisiae)	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20200310	MGI			PMID:26203146
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001102	small superior vagus ganglion		IEA		N	RGD:5509061	20181227	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19211677
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20181227	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509342
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19211677
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19211677
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509342
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19211677
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20181227	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23348741
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23348741
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19211677
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19211677
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19211677
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19211677
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23318132
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24413433
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23348741
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19211677
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20181227	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0009268	absent cerebellum fissure		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20150226	MGI			PMID:24589552
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20161208	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509342
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0010008	abnormal Purkinje cell migration		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509342
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20181227	MGI			
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23348741
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0013507	increased ovary apoptosis		IAGP		N	RGD:5509061	20161208	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20161208	MGI			PMID:17543860
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0030024	abnormal meiotic attachment of telomere to nuclear envelope		IAGP		N	RGD:5509061	20170803	MGI			PMID:24413433
1550518	Sun1	Sad1 and UNC84 domain containing 1	gene	MP:0030024	abnormal meiotic attachment of telomere to nuclear envelope		IAGP		N	RGD:5509061	20191024	MGI			PMID:30718482
1550519	Spg21	SPG21, maspardin	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1550519	Spg21	SPG21, maspardin	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20210318	MGI			PMID:20661613
1550519	Spg21	SPG21, maspardin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210318	MGI			PMID:20661613
1550519	Spg21	SPG21, maspardin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210318	MGI			PMID:26978163
1550519	Spg21	SPG21, maspardin	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1550519	Spg21	SPG21, maspardin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20210318	MGI			PMID:26978163
1550519	Spg21	SPG21, maspardin	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:20661613
1550519	Spg21	SPG21, maspardin	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:26978163
1550519	Spg21	SPG21, maspardin	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:26978163
1550519	Spg21	SPG21, maspardin	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20210318	MGI			PMID:26978163
1550519	Spg21	SPG21, maspardin	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20260402	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:31645418
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878172
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20200709	MGI			PMID:32485164
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20200625	MGI			PMID:32485164
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20241121	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20200820	MGI			PMID:32725927
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20200820	MGI			PMID:32725927
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075344
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200416	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200416	MGI			PMID:24800825
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200416	MGI			PMID:27019629
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200820	MGI			PMID:31645418
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20200625	MGI			PMID:32485164
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075344
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20200625	MGI			PMID:32485164
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200820	MGI			PMID:31645418
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20200416	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003136	yellow coat color		IEA		N	RGD:5509061	20170323	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003184	increased angiotensin I-converting enzyme activity		IAGP		N	RGD:5509061	20200416	MGI			PMID:27019629
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003288	intestinal edema		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003292	melena		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20200820	MGI			PMID:29570986
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003819	increased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20200416	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20200416	MGI			PMID:24800825
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0004013	decreased pulmonary artery pressure		IAGP		N	RGD:5509061	20200820	MGI			PMID:29570986
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20160331	MGI			PMID:25448263
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12075344
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200416	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20200416	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878172
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20200820	MGI			PMID:32725927
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005573	increased pulmonary respiratory rate		IAGP		N	RGD:5509061	20200416	MGI			PMID:27019629
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200416	MGI			PMID:27019629
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20200820	MGI			PMID:32725927
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878172
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20160331	MGI			PMID:25448263
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20200625	MGI			PMID:32485164
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0008629	increased circulating interleukin-9 level		IAGP		N	RGD:5509061	20200625	MGI			PMID:32485164
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200820	MGI			PMID:31645418
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20160331	MGI			PMID:25448263
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20200820	MGI			PMID:31645418
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20200625	MGI			PMID:32485164
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0011044	increased lung elastance		IAGP		N	RGD:5509061	20200416	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0012041	increased susceptibility to pulmonary hyaline membrane formation		IAGP		N	RGD:5509061	20200416	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0012041	increased susceptibility to pulmonary hyaline membrane formation		IAGP		N	RGD:5509061	20200416	MGI			PMID:24800825
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160331	MGI			PMID:25448263
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20210128	MGI			PMID:33097186
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20200416	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0020446	increased NAD(P)H oxidase activity		IAGP		N	RGD:5509061	20171116	MGI			PMID:17499227
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0020861	abnormal cornea wound healing		IAGP		N	RGD:5509061	20200820	MGI			PMID:32725927
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:24800825
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200625	MGI			PMID:32485164
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20251023	MGI			PMID:35690792
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0020950	decreased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16007097
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:12075344
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:24800825
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031228	decreased angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031229	increased angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031229	increased angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031229	increased angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16878172
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031231	decreased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031232	increased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16001071
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031232	increased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16505206
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031232	increased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16878172
1550521	Ace2	angiotensin converting enzyme 2	gene	MP:0031319	impaired intestine regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:33097186
1550522	Guca2a	guanylate cyclase activator 2a (guanylin)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1550522	Guca2a	guanylate cyclase activator 2a (guanylin)	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1550522	Guca2a	guanylate cyclase activator 2a (guanylin)	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12466132
1550522	Guca2a	guanylate cyclase activator 2a (guanylin)	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12466132
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20160630	MGI			PMID:26888934
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160630	MGI			PMID:26888934
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20240523	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20160630	MGI			PMID:26888934
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20201022	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:26888934
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20160630	MGI			PMID:26888934
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20160630	MGI			PMID:26888934
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20210128	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0010571	shortened ST segment		IEA		N	RGD:5509061	20210128	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160630	MGI			PMID:26888934
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0011954	shortened PQ interval		IEA		N	RGD:5509061	20210128	MGI			
1550523	Sorbs2	sorbin and SH3 domain containing 2	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:26888934
1550524	Rps6kc1	ribosomal protein S6 kinase C1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20250508	MGI			
1550524	Rps6kc1	ribosomal protein S6 kinase C1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1550524	Rps6kc1	ribosomal protein S6 kinase C1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1550524	Rps6kc1	ribosomal protein S6 kinase C1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1550524	Rps6kc1	ribosomal protein S6 kinase C1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20241121	MGI			
1550524	Rps6kc1	ribosomal protein S6 kinase C1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20240523	MGI			
1550524	Rps6kc1	ribosomal protein S6 kinase C1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1550525	Meis1	Meis homeobox 1	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20151022	MGI			PMID:25363539
1550525	Meis1	Meis homeobox 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1550525	Meis1	Meis homeobox 1	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1550525	Meis1	Meis homeobox 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20240801	MGI			PMID:38314840
1550525	Meis1	Meis homeobox 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1550525	Meis1	Meis homeobox 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20151022	MGI			PMID:25363539
1550525	Meis1	Meis homeobox 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22995899
1550525	Meis1	Meis homeobox 1	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22995899
1550525	Meis1	Meis homeobox 1	gene	MP:0003714	absent platelets		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20151022	MGI			PMID:25363539
1550525	Meis1	Meis homeobox 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22995899
1550525	Meis1	Meis homeobox 1	gene	MP:0008253	absent megakaryocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0008253	absent megakaryocytes		IAGP		N	RGD:5509061	20151022	MGI			PMID:25363539
1550525	Meis1	Meis homeobox 1	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22995899
1550525	Meis1	Meis homeobox 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20201022	MGI			
1550525	Meis1	Meis homeobox 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1550525	Meis1	Meis homeobox 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20151022	MGI			PMID:25363539
1550525	Meis1	Meis homeobox 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22995899
1550525	Meis1	Meis homeobox 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550525	Meis1	Meis homeobox 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882575
1550525	Meis1	Meis homeobox 1	gene	MP:0014638	increased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:38314840
1550525	Meis1	Meis homeobox 1	gene	MP:0020327	abnormal capillary branching pattern		IAGP		N	RGD:5509061	20160714	MGI			PMID:14713950
1550525	Meis1	Meis homeobox 1	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20240801	MGI			PMID:38314840
1550527	Skic2	SKI2 subunit of superkiller complex	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20230720	MGI			
1550527	Skic2	SKI2 subunit of superkiller complex	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20230720	MGI			
1550527	Skic2	SKI2 subunit of superkiller complex	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1550527	Skic2	SKI2 subunit of superkiller complex	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230720	MGI			
1550527	Skic2	SKI2 subunit of superkiller complex	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230720	MGI			
1550529	Hyal1	hyaluronoglucosaminidase 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344557
1550529	Hyal1	hyaluronoglucosaminidase 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344557
1550529	Hyal1	hyaluronoglucosaminidase 1	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344557
1550529	Hyal1	hyaluronoglucosaminidase 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:18344557
1550529	Hyal1	hyaluronoglucosaminidase 1	gene	MP:0014429	increased hyaluronic acid level		IAGP		N	RGD:5509061	20240425	MGI			PMID:18344557
1550532	Ttll4	tubulin tyrosine ligase-like family, member 4	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1550532	Ttll4	tubulin tyrosine ligase-like family, member 4	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20200310	MGI			
1550532	Ttll4	tubulin tyrosine ligase-like family, member 4	gene	MP:0001413	abnormal response to new environment		IEA		N	RGD:5509061	20200310	MGI			
1550532	Ttll4	tubulin tyrosine ligase-like family, member 4	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20200310	MGI			
1550533	Katna1	katanin p60 (ATPase-containing) subunit A1	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20200514	MGI			
1550533	Katna1	katanin p60 (ATPase-containing) subunit A1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20200514	MGI			
1550533	Katna1	katanin p60 (ATPase-containing) subunit A1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20200514	MGI			
1550533	Katna1	katanin p60 (ATPase-containing) subunit A1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200409	MGI			PMID:31685876
1550533	Katna1	katanin p60 (ATPase-containing) subunit A1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:31685876
1550533	Katna1	katanin p60 (ATPase-containing) subunit A1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200409	MGI			PMID:31685876
1550533	Katna1	katanin p60 (ATPase-containing) subunit A1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550533	Katna1	katanin p60 (ATPase-containing) subunit A1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20200409	MGI			PMID:31685876
1550533	Katna1	katanin p60 (ATPase-containing) subunit A1	gene	MP:0030981	abnormal dentate gyrus subgranular zone morphology		IAGP		N	RGD:5509061	20200409	MGI			PMID:31685876
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200514	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20200514	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200514	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20200310	MGI			PMID:17329413
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200514	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0003896	prolonged PR interval		IEA		N	RGD:5509061	20210520	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004528	fused outer hair cell stereocilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004597	increased susceptibility to noise-induced hearing loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004628	Deiters cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0004749	nonsyndromic hearing loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200514	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200514	MGI			
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:17329413
1550534	Usp53	ubiquitin specific peptidase 53	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:26609154
1550536	Gdf6	growth differentiation factor 6	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20111116	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0001963	abnormal hearing physiology		IEA		N	RGD:5509061	20111116	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0002082	postnatal lethality		IEA		N	RGD:5509061	20111116	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0003189	fused joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0004602	abnormal vertebral articular process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0005110	absent talus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0005508	abnormal skeleton morphology		IEA		N	RGD:5509061	20111116	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20111116	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0008372	small malleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550536	Gdf6	growth differentiation factor 6	gene	MP:0030106	small incus		IAGP		N	RGD:5509061	20170928	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0030108	abnormal incudostapedial joint morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0030109	abnormal incudomalleolar joint morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0030123	small middle ear ossicles		IAGP		N	RGD:5509061	20170928	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0030127	small stapes		IAGP		N	RGD:5509061	20170928	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0030349	absent coronal suture		IAGP		N	RGD:5509061	20171116	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0030400	abnormal stapes annular ligament morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:12606286
1550536	Gdf6	growth differentiation factor 6	gene	MP:0030401	absent stapes annular ligament		IAGP		N	RGD:5509061	20171207	MGI			PMID:12606286
1550537	Psd	pleckstrin and Sec7 domain containing	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1550537	Psd	pleckstrin and Sec7 domain containing	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210128	MGI			
1550537	Psd	pleckstrin and Sec7 domain containing	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1550542	Vwa5a	von Willebrand factor A domain containing 5A	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20200402	MGI			
1550542	Vwa5a	von Willebrand factor A domain containing 5A	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1550542	Vwa5a	von Willebrand factor A domain containing 5A	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20240523	MGI			
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:31837519
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20201210	MGI			PMID:32693190
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20201029	MGI			PMID:31837519
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:31837519
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0008837	increased transforming growth factor beta level		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20201029	MGI			PMID:31837519
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20250731	MGI			PMID:38733581
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20201210	MGI			PMID:32693190
1550543	Slc16a3	solute carrier family 16 (monocarboxylic acid transporters), member 3	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:32693190
1550544	Cgrrf1	cell growth regulator with ring finger domain 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1550544	Cgrrf1	cell growth regulator with ring finger domain 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20200402	MGI			
1550544	Cgrrf1	cell growth regulator with ring finger domain 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1550544	Cgrrf1	cell growth regulator with ring finger domain 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1550544	Cgrrf1	cell growth regulator with ring finger domain 1	gene	MP:0008346	increased gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1550544	Cgrrf1	cell growth regulator with ring finger domain 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1550544	Cgrrf1	cell growth regulator with ring finger domain 1	gene	MP:0013421	increased CD5-positive gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1550545	Usp29	ubiquitin specific peptidase 29	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1550545	Usp29	ubiquitin specific peptidase 29	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1550545	Usp29	ubiquitin specific peptidase 29	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20181220	MGI			PMID:27327533
1550545	Usp29	ubiquitin specific peptidase 29	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1550545	Usp29	ubiquitin specific peptidase 29	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20181220	MGI			PMID:27327533
1550545	Usp29	ubiquitin specific peptidase 29	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1550545	Usp29	ubiquitin specific peptidase 29	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:27327533
1550545	Usp29	ubiquitin specific peptidase 29	gene	MP:0010723	paternal effect		IAGP		N	RGD:5509061	20181220	MGI			PMID:27327533
1550547	Tspyl4	TSPY-like 4	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20220811	MGI			
1550547	Tspyl4	TSPY-like 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1550547	Tspyl4	TSPY-like 4	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20220811	MGI			
1550548	Rnf139	ring finger protein 139	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:26319415
1550548	Rnf139	ring finger protein 139	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26319415
1550548	Rnf139	ring finger protein 139	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26319415
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0003891	increased allantois apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0004559	small allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0008932	abnormal embryonic tissue physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0012183	decreased paraxial mesoderm size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0012183	decreased paraxial mesoderm size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0012184	absent paraxial mesoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611414
1550550	Ddx11	DEAD/H box helicase 11	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22678773
1550552	Septin2	septin 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1550552	Septin2	septin 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1550552	Septin2	septin 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1550552	Septin2	septin 2	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20230914	MGI			PMID:36378242
1550552	Septin2	septin 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1550552	Septin2	septin 2	gene	MP:0005386	behavior/neurological phenotype		IAGP		N	RGD:5509061	20230914	MGI			PMID:36378242
1550552	Septin2	septin 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1550552	Septin2	septin 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1550552	Septin2	septin 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1550552	Septin2	septin 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1550553	Otub2	OTU domain, ubiquitin aldehyde binding 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240606	MGI			PMID:36288705
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0004781	abnormal surfactant composition		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0009908	protruding tongue		IEA		N	RGD:5509061	20210520	MGI			
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0010903	abnormal pulmonary alveolus wall morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0010993	decreased surfactant secretion		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:26252542
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550555	Rcn3	reticulocalbin 3, EF-hand calcium binding domain	gene	MP:0031006	increased lung glycogen level		IAGP		N	RGD:5509061	20200130	MGI			PMID:26252542
1550557	Spata4	spermatogenesis associated 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1550559	Rttn	rotatin	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20210826	MGI			
1550559	Rttn	rotatin	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1550559	Rttn	rotatin	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1550559	Rttn	rotatin	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20111116	MGI			
1550559	Rttn	rotatin	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900971
1550559	Rttn	rotatin	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1550559	Rttn	rotatin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900971
1550559	Rttn	rotatin	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900971
1550559	Rttn	rotatin	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1550559	Rttn	rotatin	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900971
1550559	Rttn	rotatin	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210826	MGI			
1550559	Rttn	rotatin	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1550559	Rttn	rotatin	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900971
1550559	Rttn	rotatin	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900971
1550559	Rttn	rotatin	gene	MP:0004712	notochord degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900971
1550559	Rttn	rotatin	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900971
1550559	Rttn	rotatin	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1550559	Rttn	rotatin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11900971
1550559	Rttn	rotatin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1550559	Rttn	rotatin	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1550559	Rttn	rotatin	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1550561	Pitpnm1	phosphatidylinositol transfer protein, membrane-associated 1	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23820044
1550561	Pitpnm1	phosphatidylinositol transfer protein, membrane-associated 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23820044
1550561	Pitpnm1	phosphatidylinositol transfer protein, membrane-associated 1	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:23820044
1550561	Pitpnm1	phosphatidylinositol transfer protein, membrane-associated 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23820044
1550561	Pitpnm1	phosphatidylinositol transfer protein, membrane-associated 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200310	MGI			
1550561	Pitpnm1	phosphatidylinositol transfer protein, membrane-associated 1	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20200310	MGI			
1550564	Ddx5	DEAD box helicase 5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220707	MGI			PMID:33666296
1550564	Ddx5	DEAD box helicase 5	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220707	MGI			PMID:33666296
1550564	Ddx5	DEAD box helicase 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220707	MGI			PMID:33666296
1550564	Ddx5	DEAD box helicase 5	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22986526
1550564	Ddx5	DEAD box helicase 5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220707	MGI			PMID:33666296
1550564	Ddx5	DEAD box helicase 5	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220707	MGI			PMID:33666296
1550564	Ddx5	DEAD box helicase 5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220707	MGI			PMID:33666296
1550564	Ddx5	DEAD box helicase 5	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220707	MGI			PMID:33666296
1550564	Ddx5	DEAD box helicase 5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220707	MGI			PMID:33666296
1550564	Ddx5	DEAD box helicase 5	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20220707	MGI			PMID:33666296
1550566	Arf4	ARF GTPase 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1550566	Arf4	ARF GTPase 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1550566	Arf4	ARF GTPase 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170504	MGI			
1550566	Arf4	ARF GTPase 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20201015	MGI			PMID:24586199
1550566	Arf4	ARF GTPase 4	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20201015	MGI			PMID:24586199
1550566	Arf4	ARF GTPase 4	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20141003	MGI			PMID:23050017
1550566	Arf4	ARF GTPase 4	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1550566	Arf4	ARF GTPase 4	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230601	MGI			
1550566	Arf4	ARF GTPase 4	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23050017
1550566	Arf4	ARF GTPase 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:24586199
1550566	Arf4	ARF GTPase 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550566	Arf4	ARF GTPase 4	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:24586199
1550566	Arf4	ARF GTPase 4	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1550566	Arf4	ARF GTPase 4	gene	MP:0014372	decreased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240328	MGI			PMID:23050017
1550566	Arf4	ARF GTPase 4	gene	MP:0014621	abnormal brain alpha wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0014622	abnormal brain beta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0014624	abnormal brain delta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:31201232
1550566	Arf4	ARF GTPase 4	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20240328	MGI			PMID:23050017
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20241121	MGI			
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241121	MGI			
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0004085	abnormal heartbeat		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0004567	decreased myocardial fiber number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0004781	abnormal surfactant composition		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0010889	small alveolar lamellar bodies		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19515693
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17611541
1550568	Tmem38b	transmembrane protein 38B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20200310	MGI			PMID:9707118
1550574	Oprl1	opioid receptor-like 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:9707118
1550574	Oprl1	opioid receptor-like 1	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15030410
1550574	Oprl1	opioid receptor-like 1	gene	MP:0001968	abnormal touch/nociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:9155012
1550574	Oprl1	opioid receptor-like 1	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:9660760
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20200310	MGI			PMID:9707118
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20231207	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:16519664
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002735	abnormal chemical nociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:12814369
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002735	abnormal chemical nociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:9155012
1550574	Oprl1	opioid receptor-like 1	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:9707118
1550574	Oprl1	opioid receptor-like 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9707118
1550574	Oprl1	opioid receptor-like 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:12814369
1550574	Oprl1	opioid receptor-like 1	gene	MP:0004597	increased susceptibility to noise-induced hearing loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:9155012
1550574	Oprl1	opioid receptor-like 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1550574	Oprl1	opioid receptor-like 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:11027224
1550574	Oprl1	opioid receptor-like 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20210128	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220519	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210520	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1550576	Acoxl	acyl-Coenzyme A oxidase-like	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0001500	decreased kindling response		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18488037
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0002806	abnormal conditioned emotional response		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18488037
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0003459	increased fear-related response		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0003627	abnormal leukocyte tethering or rolling		IAGP		N	RGD:5509061	20141003	MGI			PMID:17111351
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18488037
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18488037
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:18488037
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0008831	abnormal insulin-like growth factor I level		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0012286	decreased frequency of paradoxical sleep		IAGP		N	RGD:5509061	20161229	MGI			PMID:25066807
1550578	St3gal4	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:22700726
1550581	Rps6ka2	ribosomal protein S6 kinase A2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22997248
1550581	Rps6ka2	ribosomal protein S6 kinase A2	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22997248
1550581	Rps6ka2	ribosomal protein S6 kinase A2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22997248
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729207
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16700072
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729207
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0001934	increased litter size		IAGP		N	RGD:5509061	20210325	MGI			PMID:30942852
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16700072
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729207
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0002772	brachypodia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729207
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19079247
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0004648	decreased thoracic vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19079247
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729207
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0006394	abnormal vertebral epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729207
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18446812
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0009874	abnormal interdigital cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18729207
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950124
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467359
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0012182	abnormal presomitic mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18257070
1550582	Sfrp2	secreted frizzled-related protein 2	gene	MP:0031411	increased ovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:30942852
1550583	Nup35	nucleoporin 35	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550583	Nup35	nucleoporin 35	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550583	Nup35	nucleoporin 35	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550583	Nup35	nucleoporin 35	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550583	Nup35	nucleoporin 35	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550583	Nup35	nucleoporin 35	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20190502	MGI			
1550583	Nup35	nucleoporin 35	gene	MP:0009536	abnormal interstitial cell of Cajal morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550583	Nup35	nucleoporin 35	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1550583	Nup35	nucleoporin 35	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550583	Nup35	nucleoporin 35	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550583	Nup35	nucleoporin 35	gene	MP:0014033	abnormal submucosal gland morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550583	Nup35	nucleoporin 35	gene	MP:0014221	increased colon goblet cell number		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550583	Nup35	nucleoporin 35	gene	MP:0014231	intestinal mucus accumulation		IAGP		N	RGD:5509061	20180517	MGI			PMID:27427419
1550586	Cuedc1	CUE domain containing 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20221215	MGI			
1550586	Cuedc1	CUE domain containing 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1550586	Cuedc1	CUE domain containing 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20221215	MGI			
1550586	Cuedc1	CUE domain containing 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251634
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251634
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251634
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251634
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251634
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19332875
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12426564
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19332875
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12426564
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251634
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19332875
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0008876	decreased uterine NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17100879
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19251634
1550588	Hcst	hematopoietic cell signal transducer	gene	MP:0012529	abnormal decidua basalis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15878887
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19430495
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24657168
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0003010	decreased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19430495
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20151224	MGI			PMID:24657168
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19430495
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0004546	esophagus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19430495
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20151224	MGI			PMID:24657168
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19430495
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:19430495
1550594	Ip6k2	inositol hexaphosphate kinase 2	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19430495
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0009879	abnormal arcus anterior morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0012398	decreased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550599	Pcgf6	polycomb group ring finger 6	gene	MP:0030989	decreased spongiotrophoblast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28304275
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20200310	MGI			
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20200310	MGI			
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:26677943
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0002102	abnormal ear morphology		IEA		N	RGD:5509061	20200310	MGI			
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26677943
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004364	thin stria vascularis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26677943
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:26677943
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20200310	MGI			PMID:26677943
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004750	syndromic hearing loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20200310	MGI			PMID:26677943
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0009517	abnormal salivary gland duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:23979167
1550600	Marveld2	MARVEL (membrane-associating) domain containing 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:26677943
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19946331
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:19946331
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20260813	MGI			PMID:42310454
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19946331
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0011198	absent proamniotic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19946331
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350561
1550602	Usp7	ubiquitin specific peptidase 7	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20260813	MGI			PMID:42310454
1550604	Zp3r	zona pellucida 3 receptor	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1550604	Zp3r	zona pellucida 3 receptor	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1550606	Rab11fip4	RAB11 family interacting protein 4 (class II)	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1550606	Rab11fip4	RAB11 family interacting protein 4 (class II)	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20240627	MGI			
1550606	Rab11fip4	RAB11 family interacting protein 4 (class II)	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1550606	Rab11fip4	RAB11 family interacting protein 4 (class II)	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1550606	Rab11fip4	RAB11 family interacting protein 4 (class II)	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1550606	Rab11fip4	RAB11 family interacting protein 4 (class II)	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201231	MGI			
1550606	Rab11fip4	RAB11 family interacting protein 4 (class II)	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1550607	Igsf21	immunoglobulin superfamily, member 21	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28864826
1550607	Igsf21	immunoglobulin superfamily, member 21	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20200310	MGI			PMID:28864826
1550607	Igsf21	immunoglobulin superfamily, member 21	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:28864826
1550609	Trim55	tripartite motif-containing 55	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1550609	Trim55	tripartite motif-containing 55	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0004094	abnormal M line morphology		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250911	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1550609	Trim55	tripartite motif-containing 55	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0010226	increased quadriceps weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210128	MGI			
1550609	Trim55	tripartite motif-containing 55	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20200827	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1550609	Trim55	tripartite motif-containing 55	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:23512667
1550609	Trim55	tripartite motif-containing 55	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:18157088
1550609	Trim55	tripartite motif-containing 55	gene	MP:0020950	decreased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:26452100
1550610	Pros1	protein S (alpha)	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0000606	decreased hepatocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0005607	decreased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0009275	bruising		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0010022	brain vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19567881
1550610	Pros1	protein S (alpha)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729839
1550610	Pros1	protein S (alpha)	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200924	MGI			PMID:19567881
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802532
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20230119	MGI			
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230119	MGI			
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802532
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802532
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0005237	abnormal olfactory tract morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802532
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802532
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0009954	abnormal mitral cell morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802532
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1550611	Ptbp2	polypyrimidine tract binding protein 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20260402	MGI			
1550612	Snip1	Smad nuclear interacting protein 1	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20241031	MGI			PMID:37027487
1550612	Snip1	Smad nuclear interacting protein 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20241031	MGI			PMID:37027487
1550612	Snip1	Smad nuclear interacting protein 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20141003	MGI			
1550612	Snip1	Smad nuclear interacting protein 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1550612	Snip1	Smad nuclear interacting protein 1	gene	MP:0006241	abnormal placement of pupils		IEA		N	RGD:5509061	20141003	MGI			
1550612	Snip1	Smad nuclear interacting protein 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20241031	MGI			PMID:37027487
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20200310	MGI			
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20221215	MGI			
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20250508	MGI			
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20221215	MGI			
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20200310	MGI			
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:27466202
1550613	Zbtb24	zinc finger and BTB domain containing 24	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550617	Larp4b	La ribonucleoprotein 4B	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1550617	Larp4b	La ribonucleoprotein 4B	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1550617	Larp4b	La ribonucleoprotein 4B	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1550619	Stk16	serine/threonine kinase 16	gene	MP:0000955	abnormal spinal cord morphology		IEA		N	RGD:5509061	20210826	MGI			
1550619	Stk16	serine/threonine kinase 16	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1550619	Stk16	serine/threonine kinase 16	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1550619	Stk16	serine/threonine kinase 16	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1550620	Rhox5	reproductive homeobox 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:9769172
1550621	Creb3l4	cAMP responsive element binding protein 3-like 4	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107712
1550621	Creb3l4	cAMP responsive element binding protein 3-like 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107712
1550621	Creb3l4	cAMP responsive element binding protein 3-like 4	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16999736
1550621	Creb3l4	cAMP responsive element binding protein 3-like 4	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16999736
1550621	Creb3l4	cAMP responsive element binding protein 3-like 4	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:16107712
1550622	Hbb-bh1	hemoglobin Z, beta-like embryonic chain	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17077320
1550623	Ssc4d	scavenger receptor cysteine rich family, 4 domains	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1550627	Sh2d2a	SH2 domain containing 2A	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587356
1550627	Sh2d2a	SH2 domain containing 2A	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587356
1550627	Sh2d2a	SH2 domain containing 2A	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587356
1550627	Sh2d2a	SH2 domain containing 2A	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10587356
1550632	Glt8d1	glycosyltransferase 8 domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1550632	Glt8d1	glycosyltransferase 8 domain containing 1	gene	MP:0002635	reduced sensorimotor gating		IEA		N	RGD:5509061	20170406	MGI			
1550636	Vil1	villin 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1550636	Vil1	villin 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:10459016
1550636	Vil1	villin 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:23520048
1550636	Vil1	villin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:9438428
1550636	Vil1	villin 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1550636	Vil1	villin 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1550636	Vil1	villin 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1550636	Vil1	villin 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1550636	Vil1	villin 1	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210520	MGI			
1550637	Clk1	CDC-like kinase 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20200310	MGI			
1550637	Clk1	CDC-like kinase 1	gene	MP:0000334	decreased granulocyte number		IEA		N	RGD:5509061	20200310	MGI			
1550637	Clk1	CDC-like kinase 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20200310	MGI			
1550637	Clk1	CDC-like kinase 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1550637	Clk1	CDC-like kinase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20200310	MGI			
1550637	Clk1	CDC-like kinase 1	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20200310	MGI			
1550637	Clk1	CDC-like kinase 1	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20200310	MGI			
1550637	Clk1	CDC-like kinase 1	gene	MP:0005316	abnormal response to tactile stimuli		IEA		N	RGD:5509061	20200310	MGI			
1550638	Atp2b4	ATPase, Ca++ transporting, plasma membrane 4	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178683
1550638	Atp2b4	ATPase, Ca++ transporting, plasma membrane 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15078889
1550638	Atp2b4	ATPase, Ca++ transporting, plasma membrane 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178683
1550638	Atp2b4	ATPase, Ca++ transporting, plasma membrane 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15078889
1550638	Atp2b4	ATPase, Ca++ transporting, plasma membrane 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178683
1550638	Atp2b4	ATPase, Ca++ transporting, plasma membrane 4	gene	MP:0002742	enlarged submandibular lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178683
1550638	Atp2b4	ATPase, Ca++ transporting, plasma membrane 4	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15178683
1550638	Atp2b4	ATPase, Ca++ transporting, plasma membrane 4	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15078889
1550638	Atp2b4	ATPase, Ca++ transporting, plasma membrane 4	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20190829	MGI			PMID:28714864
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15469968
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15469968
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15469968
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15469968
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19217292
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0003371	decreased circulating estrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15469968
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0008870	increased mature ovarian follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15469968
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0013609	abnormal ovarian medulla morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0013778	abnormal mammary gland myoepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0013781	abnormal mammary gland luminal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0013908	small lateral ventricles		IAGP		N	RGD:5509061	20200310	MGI			PMID:15469968
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0015020	thin cerebral cortex layer		IAGP		N	RGD:5509061	20260716	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0015021	thick cerebral cortex layer		IAGP		N	RGD:5509061	20260716	MGI			PMID:15882580
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:20628571
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:25038044
1550640	Id4	inhibitor of DNA binding 4	gene	MP:0031383	increased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:25038044
1550646	Yif1b	Yip1 interacting factor homolog B (S. cerevisiae)	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:26077767
1550646	Yif1b	Yip1 interacting factor homolog B (S. cerevisiae)	gene	MP:0030949	abnormal Golgi vesicle transport		IAGP		N	RGD:5509061	20200402	MGI			PMID:26077767
1550646	Yif1b	Yip1 interacting factor homolog B (S. cerevisiae)	gene	MP:0030953	abnormal Golgi cisterna morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:26077767
1550647	Unc13d	unc-13 homolog D	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16688530
1550647	Unc13d	unc-13 homolog D	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20160714	MGI			PMID:23659589
1550647	Unc13d	unc-13 homolog D	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20160714	MGI			PMID:23659589
1550647	Unc13d	unc-13 homolog D	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20160714	MGI			PMID:23659589
1550647	Unc13d	unc-13 homolog D	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0008523	absent lymph node germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23659589
1550647	Unc13d	unc-13 homolog D	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20160714	MGI			PMID:23659589
1550647	Unc13d	unc-13 homolog D	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0020215	impaired blood coagulation		IAGP		N	RGD:5509061	20160714	MGI			PMID:23659589
1550647	Unc13d	unc-13 homolog D	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16688530
1550647	Unc13d	unc-13 homolog D	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16688530
1550647	Unc13d	unc-13 homolog D	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17420270
1550647	Unc13d	unc-13 homolog D	gene	MP:0031070	hemophagocytosis		IAGP		N	RGD:5509061	20200618	MGI			PMID:17420270
1550649	Cltb	clathrin light chain B	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20230216	MGI			PMID:32907943
1550649	Cltb	clathrin light chain B	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20230216	MGI			PMID:32907943
1550649	Cltb	clathrin light chain B	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20230216	MGI			PMID:32907943
1550649	Cltb	clathrin light chain B	gene	MP:0014710	increased synaptic vesicle readily releasable pool size		IAGP		N	RGD:5509061	20250814	MGI			PMID:32907943
1550650	Uxt	ubiquitously expressed prefoldin like chaperone	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20180614	MGI			PMID:29649254
1550650	Uxt	ubiquitously expressed prefoldin like chaperone	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20180614	MGI			PMID:29649254
1550650	Uxt	ubiquitously expressed prefoldin like chaperone	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20180614	MGI			PMID:29649254
1550650	Uxt	ubiquitously expressed prefoldin like chaperone	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20180614	MGI			PMID:29649254
1550650	Uxt	ubiquitously expressed prefoldin like chaperone	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20180614	MGI			PMID:29649254
1550650	Uxt	ubiquitously expressed prefoldin like chaperone	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180614	MGI			PMID:29649254
1550650	Uxt	ubiquitously expressed prefoldin like chaperone	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:29649254
1550650	Uxt	ubiquitously expressed prefoldin like chaperone	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20180614	MGI			PMID:29649254
1550651	Uba1	ubiquitin-like modifier activating enzyme 1	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1550651	Uba1	ubiquitin-like modifier activating enzyme 1	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1550651	Uba1	ubiquitin-like modifier activating enzyme 1	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:35440748
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0003121	genetic imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0014682	increased polyploid hepatocyte number		IAGP		N	RGD:5509061	20250703	MGI			PMID:16467350
1550653	Abcb7	ATP-binding cassette, sub-family B member 7	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:16467350
1550654	Pdcd10	programmed cell death 10	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20180614	MGI			PMID:24176643
1550654	Pdcd10	programmed cell death 10	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1550654	Pdcd10	programmed cell death 10	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1550654	Pdcd10	programmed cell death 10	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20180614	MGI			PMID:24176643
1550654	Pdcd10	programmed cell death 10	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21859843
1550654	Pdcd10	programmed cell death 10	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:24176643
1550654	Pdcd10	programmed cell death 10	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20180614	MGI			PMID:24176643
1550654	Pdcd10	programmed cell death 10	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0009382	abnormal cardiac jelly morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1550654	Pdcd10	programmed cell death 10	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0010503	myocardial trabeculae hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21490399
1550654	Pdcd10	programmed cell death 10	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1550654	Pdcd10	programmed cell death 10	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550654	Pdcd10	programmed cell death 10	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371769
1550654	Pdcd10	programmed cell death 10	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0000404	decreased curvature of zigzag hairs		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0008538	decreased zigzag hair amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0010130	decreased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0010134	decreased DN3 thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21258009
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0010179	rough coat		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0010202	focal dorsal hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:17635993
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550658	Zbtb17	zinc finger and BTB domain containing 17	gene	MP:0011198	absent proamniotic cavity		IAGP		N	RGD:5509061	20200310	MGI			PMID:14560010
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20231102	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674828
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674828
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674828
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036864
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0003898	abnormal QRS complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674828
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384603
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0005440	increased glycogen level		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036864
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:15674828
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20211028	MGI			PMID:27358407
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11785984
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20150416	MGI			PMID:25036864
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20211028	MGI			PMID:27358407
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20160310	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20160310	MGI			PMID:9668092
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20211028	MGI			PMID:27358407
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0014074	increased brain glycogen level		IAGP		N	RGD:5509061	20160310	MGI			PMID:10838256
1550659	Gaa	glucosidase, alpha, acid	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231102	MGI			PMID:9384603
1550660	Gsn	gelsolin	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684249
1550660	Gsn	gelsolin	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720072
1550660	Gsn	gelsolin	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720072
1550660	Gsn	gelsolin	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:10985859
1550660	Gsn	gelsolin	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684249
1550660	Gsn	gelsolin	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684249
1550660	Gsn	gelsolin	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720072
1550660	Gsn	gelsolin	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514591
1550660	Gsn	gelsolin	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720072
1550660	Gsn	gelsolin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927495
1550660	Gsn	gelsolin	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927495
1550660	Gsn	gelsolin	gene	MP:0002295	abnormal pulmonary circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654637
1550660	Gsn	gelsolin	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514591
1550660	Gsn	gelsolin	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684249
1550660	Gsn	gelsolin	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684249
1550660	Gsn	gelsolin	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654637
1550660	Gsn	gelsolin	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927495
1550660	Gsn	gelsolin	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684249
1550660	Gsn	gelsolin	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684249
1550660	Gsn	gelsolin	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720072
1550660	Gsn	gelsolin	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684249
1550660	Gsn	gelsolin	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720072
1550660	Gsn	gelsolin	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927495
1550660	Gsn	gelsolin	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10985859
1550660	Gsn	gelsolin	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20201001	MGI			PMID:7720072
1550660	Gsn	gelsolin	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684249
1550660	Gsn	gelsolin	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720072
1550660	Gsn	gelsolin	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7720072
1550660	Gsn	gelsolin	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10985859
1550660	Gsn	gelsolin	gene	MP:0013782	abnormal mammary duct terminal end bud morphology		IAGP		N	RGD:5509061	20150625	MGI			PMID:10985859
1550660	Gsn	gelsolin	gene	MP:0031723	abnormal podosome assembly		IAGP		N	RGD:5509061	20260507	MGI			PMID:10684249
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004778
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20880997
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004778
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0008361	abnormal CD8-positive, gamma-delta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004778
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0008401	abnormal CD8-positive, alpha-beta intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004778
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004778
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004778
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004778
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0008894	abnormal intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004778
1550670	H2-T3	histocompatibility 2, T region locus 3	gene	MP:0008895	abnormal intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004778
1550671	Eogt	EGF domain specific O-linked N-acetylglucosamine transferase	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20240530	MGI			PMID:28395734
1550671	Eogt	EGF domain specific O-linked N-acetylglucosamine transferase	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1550671	Eogt	EGF domain specific O-linked N-acetylglucosamine transferase	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:28395734
1550671	Eogt	EGF domain specific O-linked N-acetylglucosamine transferase	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20240530	MGI			PMID:28395734
1550671	Eogt	EGF domain specific O-linked N-acetylglucosamine transferase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0006197	ocular hypotelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0010059	olfactory bulb hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0012091	increased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17066077
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0012257	absent philtrum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18694563
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0013906	absent embryonic telencephalon		IAGP		N	RGD:5509061	20150924	MGI			PMID:12569128
1550672	Six3	sine oculis-related homeobox 3	gene	MP:0030241	absent optic pit		IAGP		N	RGD:5509061	20171109	MGI			PMID:12569128
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0002102	abnormal ear morphology		IEA		N	RGD:5509061	20210128	MGI			
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20210128	MGI			
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20250821	MGI			PMID:39241775
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0004465	degeneration of organ of Corti supporting cells		IAGP		N	RGD:5509061	20250821	MGI			PMID:39241775
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0004628	Deiters cell degeneration		IAGP		N	RGD:5509061	20250821	MGI			PMID:39241775
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20200310	MGI			
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20250821	MGI			PMID:39241775
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20250821	MGI			PMID:39241775
1550674	Mpzl2	myelin protein zero-like 2	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20250821	MGI			PMID:39241775
1550675	Lrrc28	leucine rich repeat containing 28	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20241121	MGI			
1550676	Ablim2	actin-binding LIM protein 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20221103	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20221103	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20221103	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20250508	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20221103	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20241121	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20221103	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20221103	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0011999	abnormal tail length		IEA		N	RGD:5509061	20221103	MGI			
1550677	Micu1	mitochondrial calcium uptake 1	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20201015	MGI			PMID:27477272
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230119	MGI			
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230119	MGI			
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0009695	abnormal spinal cord ventral commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20220602	MGI			PMID:35422047
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1550679	Crppa	CDP-L-ribitol pyrophosphorylase A	gene	MP:0020391	radial glial endfoot detachment		IAGP		N	RGD:5509061	20161117	MGI			PMID:23217742
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20220407	MGI			
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20220407	MGI			
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20220407	MGI			
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0002058	neonatal lethality		IEA		N	RGD:5509061	20220407	MGI			
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0002082	postnatal lethality		IEA		N	RGD:5509061	20220407	MGI			
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20260402	MGI			
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0004090	abnormal sarcomere morphology		IEA		N	RGD:5509061	20220407	MGI			
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0004819	decreased skeletal muscle mass		IEA		N	RGD:5509061	20220407	MGI			
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220407	MGI			
1550682	Mybpc1	myosin binding protein C, slow-type	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20211216	MGI			PMID:34100066
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20211216	MGI			PMID:34100066
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20200310	MGI			
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20211216	MGI			PMID:34100066
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20211216	MGI			PMID:34100066
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15782166
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15782166
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20103643
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:20103643
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20103643
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20211216	MGI			PMID:34100066
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15782166
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20211216	MGI			PMID:34100066
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20211216	MGI			PMID:34100066
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0008878	abnormal DNA methylation during gametogenesis		IAGP		N	RGD:5509061	20211216	MGI			PMID:34100066
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200310	MGI			
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20103643
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:17415412
1550683	Ewsr1	Ewing sarcoma breakpoint region 1	gene	MP:0014693	abnormal cell nucleus size		IAGP		N	RGD:5509061	20250710	MGI			PMID:17415412
1550688	Slc41a2	solute carrier family 41, member 2	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1550688	Slc41a2	solute carrier family 41, member 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550688	Slc41a2	solute carrier family 41, member 2	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0002338	abnormal pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0006054	spinal hemorrhage		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0006093	arteriovenous malformation		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179362
1550689	Fut8	fucosyltransferase 8	gene	MP:0010668	abnormal hepatic portal vein morphology		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0010856	dilated respiratory conducting tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0010903	abnormal pulmonary alveolus wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19179362
1550689	Fut8	fucosyltransferase 8	gene	MP:0010908	dilated pulmonary alveolar duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0010937	increased total lung capacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236725
1550689	Fut8	fucosyltransferase 8	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0014018	embryo tumor		IEA		N	RGD:5509061	20180628	MGI			
1550689	Fut8	fucosyltransferase 8	gene	MP:0014023	abnormal intestine placement		IEA		N	RGD:5509061	20180628	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20201022	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1550690	Synrg	synergin, gamma	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20221215	MGI			
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210520	MGI			
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:21804215
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:21804215
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21804215
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20221215	MGI			
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:21804215
1550691	Lrrc8c	leucine rich repeat containing 8 family, member C	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1550692	Inmt	indolethylamine N-methyltransferase	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1550692	Inmt	indolethylamine N-methyltransferase	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1550692	Inmt	indolethylamine N-methyltransferase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1550692	Inmt	indolethylamine N-methyltransferase	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1550694	F8	coagulation factor VIII	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705497
1550694	F8	coagulation factor VIII	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7647782
1550694	F8	coagulation factor VIII	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896409
1550694	F8	coagulation factor VIII	gene	MP:0005000	abnormal immune tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493498
1550694	F8	coagulation factor VIII	gene	MP:0005000	abnormal immune tolerance		IAGP		N	RGD:5509061	20250703	MGI			PMID:26588198
1550694	F8	coagulation factor VIII	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7647782
1550694	F8	coagulation factor VIII	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896409
1550694	F8	coagulation factor VIII	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250703	MGI			PMID:26588198
1550694	F8	coagulation factor VIII	gene	MP:0012328	decreased circulating factor VIII level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24705491
1550694	F8	coagulation factor VIII	gene	MP:0020215	impaired blood coagulation		IAGP		N	RGD:5509061	20250703	MGI			PMID:26588198
1550694	F8	coagulation factor VIII	gene	MP:0020215	impaired blood coagulation		IAGP		N	RGD:5509061	20250703	MGI			PMID:7647782
1550694	F8	coagulation factor VIII	gene	MP:0020215	impaired blood coagulation		IAGP		N	RGD:5509061	20250703	MGI			PMID:8896409
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16298139
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16298139
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965470
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965470
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20250508	MGI			
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16298139
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0002763	ectopic Bergmann glia cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15965470
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16298139
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0003894	abnormal Purkinje cell innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16298139
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1550695	Dner	delta/notch-like EGF repeat containing	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:16298139
1550696	Galnt18	polypeptide N-acetylgalactosaminyltransferase 18	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1550696	Galnt18	polypeptide N-acetylgalactosaminyltransferase 18	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200310	MGI			
1550696	Galnt18	polypeptide N-acetylgalactosaminyltransferase 18	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1550696	Galnt18	polypeptide N-acetylgalactosaminyltransferase 18	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200310	MGI			
1550696	Galnt18	polypeptide N-acetylgalactosaminyltransferase 18	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20200310	MGI			
1550696	Galnt18	polypeptide N-acetylgalactosaminyltransferase 18	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20200310	MGI			
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0010939	abnormal mandibular prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550697	Mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20200310	MGI			PMID:23267094
1550698	Klhl17	kelch-like 17	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20240523	MGI			
1550698	Klhl17	kelch-like 17	gene	MP:0000556	abnormal hindlimb morphology		IEA		N	RGD:5509061	20240523	MGI			
1550698	Klhl17	kelch-like 17	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20240523	MGI			
1550698	Klhl17	kelch-like 17	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20210819	MGI			PMID:33256713
1550698	Klhl17	kelch-like 17	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:33256713
1550698	Klhl17	kelch-like 17	gene	MP:0014373	increased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240328	MGI			PMID:33256713
1550698	Klhl17	kelch-like 17	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20210819	MGI			PMID:33256713
1550698	Klhl17	kelch-like 17	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:33256713
1550700	Stk36	serine/threonine kinase 36	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1550700	Stk36	serine/threonine kinase 36	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055716
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055716
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001867	rhinitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001893	non-obstructive hydrocephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1550700	Stk36	serine/threonine kinase 36	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1550700	Stk36	serine/threonine kinase 36	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0002959	increased urine microalbumin level		IEA		N	RGD:5509061	20211021	MGI			
1550700	Stk36	serine/threonine kinase 36	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20231207	MGI			
1550700	Stk36	serine/threonine kinase 36	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0009280	decreased activated sperm motility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055717
1550700	Stk36	serine/threonine kinase 36	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16055716
1550700	Stk36	serine/threonine kinase 36	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24525297
1550700	Stk36	serine/threonine kinase 36	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20220428	MGI			PMID:24525297
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0005310	abnormal salivary gland physiology		IAGP		N	RGD:5509061	20250807	MGI			PMID:34653670
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0011949	increased drinking frequency		IAGP		N	RGD:5509061	20250807	MGI			PMID:34653670
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0013541	abnormal submandibular gland development		IAGP		N	RGD:5509061	20250807	MGI			PMID:34653670
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0013542	abnormal submandibular gland branching morphogenesis		IAGP		N	RGD:5509061	20250807	MGI			PMID:34653670
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20201022	MGI			
1550701	Hs3st3b1	heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1550706	Rasl11b	RAS-like, family 11, member B	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1550706	Rasl11b	RAS-like, family 11, member B	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20260402	MGI			
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:29208648
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29208648
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:29208648
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29208648
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29208648
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0008957	abnormal placenta junctional zone morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29208648
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0011525	abnormal placenta intervillous maternal lacunae morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0013247	placenta necrosis		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550707	Colgalt1	collagen beta(1-O)galactosyltransferase 1	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20210506	MGI			PMID:31759980
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139386
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907072
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907072
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17296171
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20210617	MGI			PMID:19139386
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14688366
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139386
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907072
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14688366
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0006278	aortic aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139386
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:19139386
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907072
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907072
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907072
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907072
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139386
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11907072
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139386
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139386
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0010658	thoracic aorta aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139386
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17296171
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0020925	increased susceptibility to Hepadnaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11907072
1550709	Cxcl10	C-X-C motif chemokine ligand 10	gene	MP:0031274	increased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20210617	MGI			PMID:19139386
1550710	Cntfr	ciliary neurotrophic factor receptor	gene	MP:0000910	small facial motor nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585948
1550710	Cntfr	ciliary neurotrophic factor receptor	gene	MP:0000912	small trigeminal motor nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585948
1550710	Cntfr	ciliary neurotrophic factor receptor	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585948
1550710	Cntfr	ciliary neurotrophic factor receptor	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18588528
1550710	Cntfr	ciliary neurotrophic factor receptor	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585948
1550710	Cntfr	ciliary neurotrophic factor receptor	gene	MP:0001435	absent suckling reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585948
1550710	Cntfr	ciliary neurotrophic factor receptor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585948
1550710	Cntfr	ciliary neurotrophic factor receptor	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18588528
1550710	Cntfr	ciliary neurotrophic factor receptor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550713	Ufm1	ubiquitin-fold modifier 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:27545674
1550713	Ufm1	ubiquitin-fold modifier 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:27545674
1550713	Ufm1	ubiquitin-fold modifier 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27545674
1550713	Ufm1	ubiquitin-fold modifier 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:27545674
1550713	Ufm1	ubiquitin-fold modifier 1	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:27545674
1550713	Ufm1	ubiquitin-fold modifier 1	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27545674
1550713	Ufm1	ubiquitin-fold modifier 1	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20200310	MGI			PMID:27545674
1550713	Ufm1	ubiquitin-fold modifier 1	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20200310	MGI			PMID:27545674
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829355
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0001573	abnormal circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829355
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709796
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669605
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0003505	increased prolactinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709796
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0004004	patent ductus venosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18669605
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0004004	patent ductus venosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829355
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0008816	petechiae		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20829355
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0009078	adrenal gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709796
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0010128	hypovolemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20709796
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550715	Aip	aryl-hydrocarbon receptor-interacting protein	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916558
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16567502
1550717	Chmp5	charged multivesicular body protein 5	gene	MP:0014239	abnormal intracellular organelle morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:16567502
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11158324
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808453
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11158324
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808453
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:11158324
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11158324
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808453
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0000608	dissociated hepatocytes		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808453
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20210826	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:11158324
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9825865
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11158324
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:11857799
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15282747
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11158324
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16377800
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20200310	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20200310	MGI			PMID:16377800
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0003895	increased ectoderm apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0004119	hypokalemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30046000
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11158324
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16377800
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20210128	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20241121	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20200310	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12808453
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16498401
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11158324
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0012105	delayed gastrulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0012131	small visceral yolk sac		IAGP		N	RGD:5509061	20200310	MGI			PMID:7958910
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9825865
1550718	Hnf4a	hepatic nuclear factor 4, alpha	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:11158324
1550719	Dars2	aspartyl-tRNA synthetase 2 (mitochondrial)	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1550719	Dars2	aspartyl-tRNA synthetase 2 (mitochondrial)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550720	Adgrl1	adhesion G protein-coupled receptor L1	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11741895
1550720	Adgrl1	adhesion G protein-coupled receptor L1	gene	MP:0004494	abnormal synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:11741895
1550720	Adgrl1	adhesion G protein-coupled receptor L1	gene	MP:0004495	decreased synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:11741895
1550720	Adgrl1	adhesion G protein-coupled receptor L1	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:11741895
1550721	Cox6b2	cytochrome c oxidase subunit 6B2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20241107	MGI			PMID:37423748
1550721	Cox6b2	cytochrome c oxidase subunit 6B2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20241107	MGI			PMID:37423748
1550721	Cox6b2	cytochrome c oxidase subunit 6B2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20241107	MGI			PMID:37423748
1550721	Cox6b2	cytochrome c oxidase subunit 6B2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20231207	MGI			
1550721	Cox6b2	cytochrome c oxidase subunit 6B2	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20241107	MGI			PMID:37423748
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20170105	MGI			
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20190808	MGI			
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20190808	MGI			
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20170105	MGI			
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0010241	abnormal aortic arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0012749	decreased cardiac neural crest cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550725	Fgf15	fibroblast growth factor 15	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15789410
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20200310	MGI			
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0008726	increased heart left atrium size		IAGP		N	RGD:5509061	20200310	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0009870	abnormal abdominal aorta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210520	MGI			
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20200310	MGI			
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20200310	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0012557	decreased calcium uptake by cardiac muscle		IAGP		N	RGD:5509061	20200310	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0020419	decreased cardiac muscle relaxation		IAGP		N	RGD:5509061	20200310	MGI			PMID:29073106
1550726	Micu2	mitochondrial calcium uptake 2	gene	MP:0031274	increased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20210617	MGI			PMID:29073106
1550727	Acbd3	acyl-Coenzyme A binding domain containing 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20170105	MGI			
1550727	Acbd3	acyl-Coenzyme A binding domain containing 3	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1550727	Acbd3	acyl-Coenzyme A binding domain containing 3	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160421	MGI			
1550727	Acbd3	acyl-Coenzyme A binding domain containing 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1550727	Acbd3	acyl-Coenzyme A binding domain containing 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550727	Acbd3	acyl-Coenzyme A binding domain containing 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20260402	MGI			
1550733	Otof	otoferlin	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1550733	Otof	otoferlin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16024820
1550733	Otof	otoferlin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055430
1550733	Otof	otoferlin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967520
1550733	Otof	otoferlin	gene	MP:0002918	abnormal paired-pulse facilitation		IAGP		N	RGD:5509061	20191226	MGI			PMID:25253474
1550733	Otof	otoferlin	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20191226	MGI			PMID:25253474
1550733	Otof	otoferlin	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055430
1550733	Otof	otoferlin	gene	MP:0004433	abnormal cochlear inner hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055430
1550733	Otof	otoferlin	gene	MP:0004433	abnormal cochlear inner hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21451027
1550733	Otof	otoferlin	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1550733	Otof	otoferlin	gene	MP:0004562	abnormal inner hair cell synaptic ribbon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055430
1550733	Otof	otoferlin	gene	MP:0004716	abnormal cochlear nerve morphology		IAGP		N	RGD:5509061	20191226	MGI			PMID:25253474
1550733	Otof	otoferlin	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21451027
1550733	Otof	otoferlin	gene	MP:0006335	abnormal hearing electrophysiology		IAGP		N	RGD:5509061	20191226	MGI			PMID:25253474
1550733	Otof	otoferlin	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967520
1550733	Otof	otoferlin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17055430
1550733	Otof	otoferlin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1550733	Otof	otoferlin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967520
1550733	Otof	otoferlin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21451027
1550733	Otof	otoferlin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20191226	MGI			PMID:25253474
1550733	Otof	otoferlin	gene	MP:0012486	decreased cochlear VIII nucleus size		IAGP		N	RGD:5509061	20191226	MGI			PMID:25253474
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230119	MGI			
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230119	MGI			
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0002628	hepatic steatosis		IEA		N	RGD:5509061	20200310	MGI			
1550737	Agpat5	1-acylglycerol-3-phosphate O-acyltransferase 5	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1550738	Srr	serine racemase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1550738	Srr	serine racemase	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1550738	Srr	serine racemase	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1550738	Srr	serine racemase	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1550738	Srr	serine racemase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1550738	Srr	serine racemase	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483194
1550738	Srr	serine racemase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19065142
1550738	Srr	serine racemase	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19065142
1550738	Srr	serine racemase	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19065142
1550738	Srr	serine racemase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1550738	Srr	serine racemase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1550738	Srr	serine racemase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:19065142
1550738	Srr	serine racemase	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118183
1550738	Srr	serine racemase	gene	MP:0002463	abnormal neutrophil physiology		IEA		N	RGD:5509061	20150625	MGI			
1550738	Srr	serine racemase	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19065142
1550738	Srr	serine racemase	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1550738	Srr	serine racemase	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19065142
1550738	Srr	serine racemase	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19065142
1550738	Srr	serine racemase	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19118183
1550738	Srr	serine racemase	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483194
1550738	Srr	serine racemase	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19065142
1550738	Srr	serine racemase	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483194
1550738	Srr	serine racemase	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483194
1550738	Srr	serine racemase	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19483194
1550738	Srr	serine racemase	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:19065142
1550738	Srr	serine racemase	gene	MP:0030691	increased serine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:19483194
1550738	Srr	serine racemase	gene	MP:0030692	decreased serine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:19118183
1550738	Srr	serine racemase	gene	MP:0030692	decreased serine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:19483194
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20231207	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20231207	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20231207	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20231207	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20231207	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20231207	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20260402	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1550740	Qars1	glutaminyl-tRNA synthetase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
1550743	Tmx2	thioredoxin-related transmembrane protein 2	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20240926	MGI			
1550743	Tmx2	thioredoxin-related transmembrane protein 2	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191128	MGI			
1550743	Tmx2	thioredoxin-related transmembrane protein 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20191128	MGI			
1550743	Tmx2	thioredoxin-related transmembrane protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550743	Tmx2	thioredoxin-related transmembrane protein 2	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20191128	MGI			
1550743	Tmx2	thioredoxin-related transmembrane protein 2	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20191128	MGI			
1550743	Tmx2	thioredoxin-related transmembrane protein 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550744	Noa1	nitric oxide associated 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21118999
1550744	Noa1	nitric oxide associated 1	gene	MP:0013505	decreased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:21118999
1550745	Hdgfl1	HDGF like 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20200310	MGI			
1550745	Hdgfl1	HDGF like 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1550745	Hdgfl1	HDGF like 1	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20201022	MGI			PMID:32588039
1550745	Hdgfl1	HDGF like 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1550745	Hdgfl1	HDGF like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200310	MGI			
1550745	Hdgfl1	HDGF like 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550745	Hdgfl1	HDGF like 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1550746	Bzw1	basic leucine zipper and W2 domains 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20190502	MGI			
1550746	Bzw1	basic leucine zipper and W2 domains 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1550746	Bzw1	basic leucine zipper and W2 domains 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1550746	Bzw1	basic leucine zipper and W2 domains 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1550747	Gatad2a	GATA zinc finger domain containing 2A	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:17565372
1550747	Gatad2a	GATA zinc finger domain containing 2A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17565372
1550747	Gatad2a	GATA zinc finger domain containing 2A	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:17565372
1550747	Gatad2a	GATA zinc finger domain containing 2A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:17565372
1550747	Gatad2a	GATA zinc finger domain containing 2A	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17565372
1550747	Gatad2a	GATA zinc finger domain containing 2A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17565372
1550747	Gatad2a	GATA zinc finger domain containing 2A	gene	MP:0011256	abnormal neural fold morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17565372
1550748	Mrpl47	mitochondrial ribosomal protein L47	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550748	Mrpl47	mitochondrial ribosomal protein L47	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550748	Mrpl47	mitochondrial ribosomal protein L47	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20250508	MGI			
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0002899	fatigue		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0011617	abnormal habituation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:25763823
1550752	L2hgdh	L-2-hydroxyglutarate dehydrogenase	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25763823
1550753	Luc7l	Luc7-like	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15474286
1550753	Luc7l	Luc7-like	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1550753	Luc7l	Luc7-like	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1550754	Slc38a5	solute carrier family 38, member 5	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20180322	MGI			PMID:28591637
1550754	Slc38a5	solute carrier family 38, member 5	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20180322	MGI			PMID:28591637
1550754	Slc38a5	solute carrier family 38, member 5	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20180322	MGI			PMID:28591637
1550754	Slc38a5	solute carrier family 38, member 5	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:28591637
1550754	Slc38a5	solute carrier family 38, member 5	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20180322	MGI			PMID:28591637
1550754	Slc38a5	solute carrier family 38, member 5	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20180322	MGI			PMID:28591637
1550755	Akap9	A kinase anchor protein 9	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20160804	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20160804	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855593
1550755	Akap9	A kinase anchor protein 9	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23608191
1550755	Akap9	A kinase anchor protein 9	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23608191
1550755	Akap9	A kinase anchor protein 9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855593
1550755	Akap9	A kinase anchor protein 9	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23608191
1550755	Akap9	A kinase anchor protein 9	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0002216	abnormal seminiferous tubule morphology		IEA		N	RGD:5509061	20141003	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0002686	globozoospermia		IEA		N	RGD:5509061	20141003	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0002687	oligozoospermia		IEA		N	RGD:5509061	20141003	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23608191
1550755	Akap9	A kinase anchor protein 9	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0004647	decreased lumbar vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0004852	decreased testis weight		IEA		N	RGD:5509061	20141003	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0004910	decreased seminal vesicle weight		IEA		N	RGD:5509061	20141003	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23608191
1550755	Akap9	A kinase anchor protein 9	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0005567	decreased circulating total protein level		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23608191
1550755	Akap9	A kinase anchor protein 9	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855593
1550755	Akap9	A kinase anchor protein 9	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1550755	Akap9	A kinase anchor protein 9	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1550755	Akap9	A kinase anchor protein 9	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779004
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20181129	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20181129	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000389	disorganized outer root sheath cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000392	accelerated hair follicle regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000392	accelerated hair follicle regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779004
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17914447
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17914447
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001211	wrinkled skin		IEA		N	RGD:5509061	20111116	MGI			
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4618567
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001278	kinked vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001279	wavy vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779004
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001279	wavy vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001279	wavy vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:17914447
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20191031	MGI			PMID:15971077
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20141003	MGI			PMID:14779004
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20141003	MGI			
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20181129	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003813	abnormal hair follicle dermal papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003813	abnormal hair follicle dermal papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003867	increased defecation amount		IAGP		N	RGD:5509061	20191031	MGI			PMID:15971077
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20191031	MGI			PMID:15971077
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0005607	decreased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:6696991
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0008860	abnormal hair cycle telogen phase		IAGP		N	RGD:5509061	20181129	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0009351	thin hair shaft		IAGP		N	RGD:5509061	20141003	MGI			PMID:16026577
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0009351	thin hair shaft		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240817
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0010686	abnormal hair follicle matrix region morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0010686	abnormal hair follicle matrix region morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0010690	thick hair follicle outer root sheath		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0010693	thin hair follicle inner root sheath		IAGP		N	RGD:5509061	20141003	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20181129	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20191031	MGI			PMID:15971077
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0011978	abnormal potassium ion homeostasis		IAGP		N	RGD:5509061	20191031	MGI			PMID:15971077
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20191031	MGI			PMID:15971077
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0013759	decreased intestinal glucose absorption		IAGP		N	RGD:5509061	20191031	MGI			PMID:15971077
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0030575	decreased hair follicle cell proliferation		IAGP		N	RGD:5509061	20181129	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0030920	small hair follicle bulb		IAGP		N	RGD:5509061	20181220	MGI			PMID:15871460
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0030920	small hair follicle bulb		IAGP		N	RGD:5509061	20181220	MGI			PMID:16103225
1550757	Sgk3	serum/glucocorticoid regulated kinase 3	gene	MP:0030925	early exit from anagen phase		IEA		N	RGD:5509061	20181220	MGI			
1550758	Tmem45b	transmembrane protein 45b	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20221215	MGI			PMID:36322717
1550758	Tmem45b	transmembrane protein 45b	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:36322717
1550759	Hdac4	histone deacetylase 4	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672313
1550759	Hdac4	histone deacetylase 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672313
1550759	Hdac4	histone deacetylase 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200723	MGI			PMID:27884425
1550759	Hdac4	histone deacetylase 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200723	MGI			PMID:32153359
1550759	Hdac4	histone deacetylase 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200723	MGI			PMID:32153359
1550759	Hdac4	histone deacetylase 4	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20200723	MGI			PMID:32153359
1550759	Hdac4	histone deacetylase 4	gene	MP:0001432	abnormal food preference		IAGP		N	RGD:5509061	20200723	MGI			PMID:27884425
1550759	Hdac4	histone deacetylase 4	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20200723	MGI			PMID:27884425
1550759	Hdac4	histone deacetylase 4	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20200723	MGI			PMID:32153359
1550759	Hdac4	histone deacetylase 4	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672313
1550759	Hdac4	histone deacetylase 4	gene	MP:0001994	increased blinking frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672313
1550759	Hdac4	histone deacetylase 4	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20200723	MGI			PMID:32153359
1550759	Hdac4	histone deacetylase 4	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20200723	MGI			PMID:27884425
1550759	Hdac4	histone deacetylase 4	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20200723	MGI			PMID:32153359
1550759	Hdac4	histone deacetylase 4	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672313
1550759	Hdac4	histone deacetylase 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1550759	Hdac4	histone deacetylase 4	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20200723	MGI			PMID:27884425
1550759	Hdac4	histone deacetylase 4	gene	MP:0003417	premature endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672313
1550759	Hdac4	histone deacetylase 4	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20200723	MGI			PMID:32153359
1550759	Hdac4	histone deacetylase 4	gene	MP:0004243	abnormal motor nerve collateral sprouting		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007902
1550759	Hdac4	histone deacetylase 4	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20200723	MGI			PMID:27884425
1550759	Hdac4	histone deacetylase 4	gene	MP:0006432	abnormal costal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20211021	MGI			
1550759	Hdac4	histone deacetylase 4	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672313
1550759	Hdac4	histone deacetylase 4	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672313
1550759	Hdac4	histone deacetylase 4	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17786239
1550759	Hdac4	histone deacetylase 4	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20200723	MGI			PMID:32153359
1550759	Hdac4	histone deacetylase 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200723	MGI			PMID:27884425
1550759	Hdac4	histone deacetylase 4	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20200723	MGI			PMID:32153359
1550759	Hdac4	histone deacetylase 4	gene	MP:0030356	premature lambdoid suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:15537544
1550759	Hdac4	histone deacetylase 4	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:19672313
1550760	Thap4	THAP domain containing 4	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20240801	MGI			PMID:38658415
1550760	Thap4	THAP domain containing 4	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20240801	MGI			PMID:38658415
1550760	Thap4	THAP domain containing 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240801	MGI			PMID:38658415
1550760	Thap4	THAP domain containing 4	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20240801	MGI			PMID:38658415
1550761	Ccl4	C-C motif chemokine ligand 4	gene	MP:0000550	abnormal forelimb morphology		IEA		N	RGD:5509061	20240523	MGI			
1550761	Ccl4	C-C motif chemokine ligand 4	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20240502	MGI			PMID:36863097
1550761	Ccl4	C-C motif chemokine ligand 4	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20240509	MGI			PMID:36863097
1550761	Ccl4	C-C motif chemokine ligand 4	gene	MP:0012000	abnormal limb position		IEA		N	RGD:5509061	20240523	MGI			
1550764	Jmjd4	jumonji domain containing 4	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1550764	Jmjd4	jumonji domain containing 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:27147518
1550764	Jmjd4	jumonji domain containing 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1550764	Jmjd4	jumonji domain containing 4	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1550764	Jmjd4	jumonji domain containing 4	gene	MP:0005358	abnormal incisor morphology		IEA		N	RGD:5509061	20210128	MGI			
1550764	Jmjd4	jumonji domain containing 4	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1550764	Jmjd4	jumonji domain containing 4	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1550764	Jmjd4	jumonji domain containing 4	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1550764	Jmjd4	jumonji domain containing 4	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1550770	Syap1	synapse associated protein 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190725	MGI			PMID:31118165
1550770	Syap1	synapse associated protein 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190725	MGI			PMID:31118165
1550770	Syap1	synapse associated protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:27344443
1550770	Syap1	synapse associated protein 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20190725	MGI			PMID:31118165
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0008087	decreased T helper 1 cell number		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0010220	decreased T-helper 17 cell number		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550772	Slc1a5	solute carrier family 1 (neutral amino acid transporter), member 5	gene	MP:0010836	decreased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20180215	MGI			PMID:24792914
1550773	Srpk3	serine/arginine-rich protein specific kinase 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1550773	Srpk3	serine/arginine-rich protein specific kinase 3	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1550773	Srpk3	serine/arginine-rich protein specific kinase 3	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20181227	MGI			
1550773	Srpk3	serine/arginine-rich protein specific kinase 3	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16140986
1550773	Srpk3	serine/arginine-rich protein specific kinase 3	gene	MP:0002731	megacolon		IEA		N	RGD:5509061	20181227	MGI			
1550773	Srpk3	serine/arginine-rich protein specific kinase 3	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16140986
1550773	Srpk3	serine/arginine-rich protein specific kinase 3	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:16140986
1550773	Srpk3	serine/arginine-rich protein specific kinase 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918385
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001863	blood vessel inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918385
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0003875	abnormal hair follicle regression		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0004941	abnormal regulatory T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0008698	abnormal interleukin-4 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22434867
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23918385
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20220331	MGI			PMID:30367465
1550774	Drosha	drosha, ribonuclease type III	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:18725527
1550775	Atp8b3	ATPase, class I, type 8B, member 3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975727
1550775	Atp8b3	ATPase, class I, type 8B, member 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975727
1550775	Atp8b3	ATPase, class I, type 8B, member 3	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975727
1550775	Atp8b3	ATPase, class I, type 8B, member 3	gene	MP:0005410	abnormal fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975727
1550775	Atp8b3	ATPase, class I, type 8B, member 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550776	Fcgr4	Fc receptor, IgG, low affinity IV	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754379
1550776	Fcgr4	Fc receptor, IgG, low affinity IV	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974962
1550776	Fcgr4	Fc receptor, IgG, low affinity IV	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754379
1550776	Fcgr4	Fc receptor, IgG, low affinity IV	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754379
1550776	Fcgr4	Fc receptor, IgG, low affinity IV	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:20974962
1550776	Fcgr4	Fc receptor, IgG, low affinity IV	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23754379
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000436	abnormal head movements		IAGP		N	RGD:5509061	20200310	MGI			PMID:8706126
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:8706126
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8706126
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000756	forelimb paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16551741
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:18987190
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:9464989
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:9560463
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:8706126
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:8706126
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:18987190
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8706126
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:8706126
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:18987190
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20200310	MGI			PMID:10601330
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20200310	MGI			PMID:8917582
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20200310	MGI			PMID:9464989
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18987190
1550779	Ugt8a	UDP galactosyltransferase 8A	gene	MP:0014329	abnormal Purkinje cell axon morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:16551741
1550780	Rab9	RAB9, member RAS oncogene family	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1550781	Parp8	poly (ADP-ribose) polymerase family, member 8	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1550781	Parp8	poly (ADP-ribose) polymerase family, member 8	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1550781	Parp8	poly (ADP-ribose) polymerase family, member 8	gene	MP:0003064	decreased coping response		IEA		N	RGD:5509061	20210128	MGI			
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0003822	decreased left ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:22375032
1550782	Abcb8	ATP-binding cassette, sub-family B member 8	gene	MP:0020367	increased heart iron level		IAGP		N	RGD:5509061	20161020	MGI			PMID:22375032
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20240523	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002776	increased Sertoli cell number		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0003582	abnormal ovary development		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0008966	abnormal chiasmata formation		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220519	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis		IAGP		N	RGD:5509061	20160609	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0012000	abnormal limb position		IEA		N	RGD:5509061	20241121	MGI			
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0013538	increased Harderian gland adenoma incidence		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0014040	increased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20160609	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:26637282
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0030934	decreased primordial germ cell proliferation		IAGP		N	RGD:5509061	20190411	MGI			PMID:26490168
1550783	Brip1	BRCA1 interacting protein C-terminal helicase 1	gene	MP:0030935	increased primordial germ cell apoptosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:26490168
1550784	Tbcel	tubulin folding cofactor E-like	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723298
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723298
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723298
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22158707
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723298
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0004112	abnormal arteriole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723298
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20231207	MGI			
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723298
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723298
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723298
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0011401	abnormal vascular smooth muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723298
1550785	Tmsb4x	thymosin, beta 4, X chromosome	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955340
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955340
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230302	MGI			PMID:32051257
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955340
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20230302	MGI			PMID:32051257
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20230302	MGI			PMID:32051257
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20230302	MGI			PMID:32051257
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0006120	mitral valve prolapse		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20230302	MGI			PMID:32051257
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0010614	abnormal mitral valve cusp morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23955340
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:23955340
1550795	Dzip1	DAZ interacting protein 1	gene	MP:0013206	abnormal motile cilium morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1550796	Sulf1	sulfatase 1	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22298771
1550796	Sulf1	sulfatase 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16901266
1550796	Sulf1	sulfatase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16901266
1550796	Sulf1	sulfatase 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20210211	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16901266
1550796	Sulf1	sulfatase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IEA		N	RGD:5509061	20170406	MGI			
1550796	Sulf1	sulfatase 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20260402	MGI			
1550796	Sulf1	sulfatase 1	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20250508	MGI			
1550796	Sulf1	sulfatase 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004545	enlarged esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0004548	dilated esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004621	lumbar vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004622	sacral vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004687	split vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0004831	long incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20250508	MGI			
1550796	Sulf1	sulfatase 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1550796	Sulf1	sulfatase 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16901266
1550796	Sulf1	sulfatase 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17720696
1550796	Sulf1	sulfatase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17593974
1550796	Sulf1	sulfatase 1	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20150219	MGI			PMID:16901266
1550796	Sulf1	sulfatase 1	gene	MP:0011951	increased cardiac stroke volume		IEA		N	RGD:5509061	20250508	MGI			
1550796	Sulf1	sulfatase 1	gene	MP:0012279	wide sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20180125	MGI			PMID:18213582
1550796	Sulf1	sulfatase 1	gene	MP:0031088	coughing		IAGP		N	RGD:5509061	20210211	MGI			PMID:17720696
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20230601	MGI			
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22902753
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22510880
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22354172
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25063677
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26527802
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200611	MGI			PMID:32052574
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190642
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22354172
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22464327
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30224759
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17934449
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509778
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20200310	MGI			PMID:17934449
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509778
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:17934449
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509778
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17934449
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:27736879
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509778
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:17934449
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20220721	MGI			PMID:34376666
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22464327
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22895187
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:26527802
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190642
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20200310	MGI			PMID:30224759
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20211202	MGI			PMID:33431892
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23726973
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22510880
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22902753
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200611	MGI			PMID:32052574
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22510880
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20200310	MGI			PMID:23202126
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22354172
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30224759
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0008142	decreased small intestinal villus size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0008800	increased small intestinal crypt cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22354172
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30224759
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:30224759
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509778
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:23726973
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190642
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22902753
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0010156	abnormal small intestinal crypt cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26527802
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21727895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0010158	abnormal intestine development		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0010158	abnormal intestine development		IAGP		N	RGD:5509061	20200310	MGI			PMID:27736879
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0011006	abnormal epidermal stem cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200611	MGI			PMID:32052574
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509778
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17934449
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21927002
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24680895
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:30224759
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013264	tongue ankylosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15509778
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013481	abnormal ileum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22902753
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013483	abnormal jejunum crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013485	increased Paneth cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190642
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013485	increased Paneth cell number		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:27736879
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013487	abnormal Paneth cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22190642
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013648	increased CD11b-high dendritic cell number		IEA		N	RGD:5509061	20230601	MGI			
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013798	abnormal jejunal goblet cell morphology		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0013890	increased CD8-positive, CD25-positive alpha-beta T cell number		IEA		N	RGD:5509061	20230601	MGI			
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0014076	absent Paneth cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:22354172
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0014077	ectopic Paneth cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:22510880
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0014077	ectopic Paneth cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:22902753
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0014201	abnormal intestinal epithelium physiology		IAGP		N	RGD:5509061	20200409	MGI			PMID:30449703
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0014508	decreased intestinal crypt stem cell number		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0014509	abnormal intestinal crypt stem cell physiology		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0014511	increased intestinal crypt stem cell proliferation		IAGP		N	RGD:5509061	20260122	MGI			PMID:40816454
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0014754	abnormal tumor progression		IAGP		N	RGD:5509061	20250925	MGI			PMID:26527802
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0031319	impaired intestine regeneration		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1550798	Lgr5	leucine rich repeat containing G protein coupled receptor 5	gene	MP:0031320	enhanced intestine regeneration		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:19805030
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:19805030
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:19805030
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19805030
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20200310	MGI			
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19805030
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0010559	heart block		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0010732	abnormal node of Ranvier morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19805030
1550799	Sh3tc2	SH3 domain and tetratricopeptide repeats 2	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:28355569
1550801	Rcc2	regulator of chromosome condensation 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1550801	Rcc2	regulator of chromosome condensation 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200310	MGI			
1550801	Rcc2	regulator of chromosome condensation 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20200310	MGI			
1550801	Rcc2	regulator of chromosome condensation 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1550801	Rcc2	regulator of chromosome condensation 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1550801	Rcc2	regulator of chromosome condensation 2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1550801	Rcc2	regulator of chromosome condensation 2	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20201231	MGI			
1550802	Sec13	SEC13 homolog, nuclear pore and COPII coat complex component	gene	MP:0010580	decreased heart left ventricle size		IEA		N	RGD:5509061	20240523	MGI			
1550802	Sec13	SEC13 homolog, nuclear pore and COPII coat complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1550804	Actl6b	actin-like 6B	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:17920018
1550804	Actl6b	actin-like 6B	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:17920018
1550804	Actl6b	actin-like 6B	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1550804	Actl6b	actin-like 6B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1550804	Actl6b	actin-like 6B	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17920018
1550804	Actl6b	actin-like 6B	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17920018
1550804	Actl6b	actin-like 6B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17920018
1550804	Actl6b	actin-like 6B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20160421	MGI			PMID:25805847
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20160421	MGI			PMID:25805847
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160421	MGI			PMID:25805847
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:25805847
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160421	MGI			PMID:25805847
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:25805847
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20160421	MGI			PMID:25805847
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20160421	MGI			PMID:25805847
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20160421	MGI			PMID:25805847
1550806	Dpy30	dpy-30, histone methyltransferase complex regulatory subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22571926
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22571926
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22110132
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22571926
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001765	abnormal ion homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001776	abnormal circulating sodium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:22110132
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:22571926
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:23335223
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0002425	abnormal susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20200310	MGI			PMID:23335223
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22110132
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0002776	increased Sertoli cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:23335223
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0004849	abnormal testis size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22110132
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22571926
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22110132
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22110132
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22571926
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:23335223
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22110132
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22110132
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22571926
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23335223
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23335223
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0010134	decreased DN3 thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0010135	increased DN4 thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22556341
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22571926
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:22571926
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:22110132
1550809	Tsc22d3	TSC22 domain family, member 3	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:22556341
1550810	Eif4e2	eukaryotic translation initiation factor 4E member 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22751931
1550810	Eif4e2	eukaryotic translation initiation factor 4E member 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22751931
1550810	Eif4e2	eukaryotic translation initiation factor 4E member 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:22751931
1550810	Eif4e2	eukaryotic translation initiation factor 4E member 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22751931
1550810	Eif4e2	eukaryotic translation initiation factor 4E member 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22751931
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186781
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929536
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15157418
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537788
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035080
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186781
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:9546391
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0014749	abnormal olfactory bulb axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:21646512
1550812	Or10a4	olfactory receptor family 10 subfamily A member 4	gene	MP:0020348	decreased olfactory sensory neuron number		IAGP		N	RGD:5509061	20161229	MGI			PMID:23884929
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20200310	MGI			PMID:19001414
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:18815592
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:18815592
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:18815592
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18815592
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19001414
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19001414
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19001414
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:18815592
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:19001414
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:18815592
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:19001414
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0008235	increased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19001414
1550814	Npas4	neuronal PAS domain protein 4	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:19001414
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20220407	MGI			PMID:34625556
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0001876	decreased inflammatory response		IEA		N	RGD:5509061	20200310	MGI			
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23835476
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20260402	MGI			
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:23835476
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0006043	decreased apoptosis		IEA		N	RGD:5509061	20200310	MGI			
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23835476
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:24012422
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0012555	decreased cell death		IEA		N	RGD:5509061	20200310	MGI			
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20200310	MGI			PMID:24557836
1550818	Mlkl	mixed lineage kinase domain-like	gene	MP:0013648	increased CD11b-high dendritic cell number		IAGP		N	RGD:5509061	20240125	MGI			PMID:35064213
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20141003	MGI			
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20181122	MGI			PMID:28431046
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20141003	MGI			
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287714
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18955569
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18955569
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932351
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163203
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001237	enlarged spinous cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20141003	MGI			
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932351
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932351
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20160512	MGI			PMID:17637742
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163203
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160512	MGI			PMID:17637742
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932351
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24752179
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002295	abnormal pulmonary circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287714
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287714
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20141003	MGI			
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0002939	head spot		IAGP		N	RGD:5509061	20181122	MGI			PMID:28431046
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20160512	MGI			PMID:17637742
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20160512	MGI			PMID:17637742
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0003800	monodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932351
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18955569
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18955569
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932351
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18955569
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18955569
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12932351
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18955569
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163203
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0009476	enlarged cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0009483	enlarged ileum		IAGP		N	RGD:5509061	20160304	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:28431046
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20160512	MGI			PMID:17637742
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20160512	MGI			PMID:17637742
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010413	complete atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010453	abnormal coronary vein morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010482	abnormal aortic sinus morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010595	abnormal aortic valve cusp morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010656	thick myocardium		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0010998	pulmonary alveolar proteinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163203
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16192310
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20181122	MGI			PMID:28431046
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163203
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287714
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011648	thick heart valve cusps		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0011684	coronary-cameral fistula to heart right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160304	MGI			PMID:21518954
1550820	Smarca4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	gene	MP:0013958	decreased small intestine length		IAGP		N	RGD:5509061	20160304	MGI			PMID:21518954
1550821	Pkp4	plakophilin 4	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1550821	Pkp4	plakophilin 4	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220519	MGI			
1550821	Pkp4	plakophilin 4	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20170105	MGI			
1550821	Pkp4	plakophilin 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12904583
1550821	Pkp4	plakophilin 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220519	MGI			
1550821	Pkp4	plakophilin 4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220519	MGI			
1550821	Pkp4	plakophilin 4	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1550821	Pkp4	plakophilin 4	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1550821	Pkp4	plakophilin 4	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20211021	MGI			
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20240523	MGI			
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0009291	decreased femoral fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550822	Prcp	prolylcarboxypeptidase (angiotensinase C)	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620781
1550824	Ly6k	lymphocyte antigen 6 family member K	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24501175
1550824	Ly6k	lymphocyte antigen 6 family member K	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20200310	MGI			PMID:24501175
1550824	Ly6k	lymphocyte antigen 6 family member K	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220303	MGI			PMID:24501175
1550831	Mdh1b	malate dehydrogenase 1B, NAD (soluble)	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1550833	Dync1li2	dynein, cytoplasmic 1 light intermediate chain 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1550833	Dync1li2	dynein, cytoplasmic 1 light intermediate chain 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1550833	Dync1li2	dynein, cytoplasmic 1 light intermediate chain 2	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1550833	Dync1li2	dynein, cytoplasmic 1 light intermediate chain 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20220811	MGI			
1550833	Dync1li2	dynein, cytoplasmic 1 light intermediate chain 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550834	Iars2	isoleucine-tRNA synthetase 2, mitochondrial	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20200310	MGI			
1550834	Iars2	isoleucine-tRNA synthetase 2, mitochondrial	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20201022	MGI			
1550834	Iars2	isoleucine-tRNA synthetase 2, mitochondrial	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200310	MGI			
1550834	Iars2	isoleucine-tRNA synthetase 2, mitochondrial	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550834	Iars2	isoleucine-tRNA synthetase 2, mitochondrial	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1550839	Zyx	zyxin	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505170
1550839	Zyx	zyxin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482962
1550839	Zyx	zyxin	gene	MP:0011707	impaired fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505170
1550839	Zyx	zyxin	gene	MP:0011709	increased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505170
1550839	Zyx	zyxin	gene	MP:0014699	increased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:16505170
1550845	Akap6	A kinase anchor protein 6	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337591
1550845	Akap6	A kinase anchor protein 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337591
1550845	Akap6	A kinase anchor protein 6	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16337591
1550845	Akap6	A kinase anchor protein 6	gene	MP:0011915	increased heart left atrium weight		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0012688	abnormal heart ventricles weight		IAGP		N	RGD:5509061	20141120	MGI			PMID:24812305
1550845	Akap6	A kinase anchor protein 6	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:24812305
1550846	Rer1	retention in endoplasmic reticulum sorting receptor 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21187406
1550846	Rer1	retention in endoplasmic reticulum sorting receptor 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1550846	Rer1	retention in endoplasmic reticulum sorting receptor 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20200310	MGI			
1550846	Rer1	retention in endoplasmic reticulum sorting receptor 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1550846	Rer1	retention in endoplasmic reticulum sorting receptor 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20200310	MGI			PMID:21187406
1550846	Rer1	retention in endoplasmic reticulum sorting receptor 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1550846	Rer1	retention in endoplasmic reticulum sorting receptor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550846	Rer1	retention in endoplasmic reticulum sorting receptor 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1550846	Rer1	retention in endoplasmic reticulum sorting receptor 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1550847	Utp18	UTP18 small subunit processome component	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1550847	Utp18	UTP18 small subunit processome component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1550848	Klhl20	kelch-like 20	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20200310	MGI			PMID:22511632
1550848	Klhl20	kelch-like 20	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:22511632
1550848	Klhl20	kelch-like 20	gene	MP:0002161	abnormal fertility/fecundity		IEA		N	RGD:5509061	20111116	MGI			
1550848	Klhl20	kelch-like 20	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:22511632
1550848	Klhl20	kelch-like 20	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:22511632
1550848	Klhl20	kelch-like 20	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22511632
1550848	Klhl20	kelch-like 20	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:22511632
1550848	Klhl20	kelch-like 20	gene	MP:0020857	cornea epithelium hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22511632
1550849	Ccna2	cyclin A2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10864467
1550849	Ccna2	cyclin A2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:8988174
1550849	Ccna2	cyclin A2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592082
1550849	Ccna2	cyclin A2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8988174
1550852	Arr3	arrestin 3, retinal	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1550852	Arr3	arrestin 3, retinal	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701071
1550852	Arr3	arrestin 3, retinal	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20240523	MGI			
1550853	Gnb3	guanine nucleotide binding protein (G protein), beta 3	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22895717
1550853	Gnb3	guanine nucleotide binding protein (G protein), beta 3	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22895717
1550853	Gnb3	guanine nucleotide binding protein (G protein), beta 3	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22895717
1550853	Gnb3	guanine nucleotide binding protein (G protein), beta 3	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22895717
1550853	Gnb3	guanine nucleotide binding protein (G protein), beta 3	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22895717
1550853	Gnb3	guanine nucleotide binding protein (G protein), beta 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22895717
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16531066
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0001983	abnormal olfactory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16531066
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20211021	MGI			
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20211021	MGI			
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1550856	Ncam2	neural cell adhesion molecule 2	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20170314	MGI			PMID:25875008
1550857	Cep350	centrosomal protein 350	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1550857	Cep350	centrosomal protein 350	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550857	Cep350	centrosomal protein 350	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1550860	Abcc12	ATP-binding cassette, sub-family C member 12	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:33771553
1550860	Abcc12	ATP-binding cassette, sub-family C member 12	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20250821	MGI			PMID:33771553
1550860	Abcc12	ATP-binding cassette, sub-family C member 12	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20250821	MGI			PMID:33771553
1550860	Abcc12	ATP-binding cassette, sub-family C member 12	gene	MP:0003252	abnormal bile duct physiology		IAGP		N	RGD:5509061	20250821	MGI			PMID:33771553
1550860	Abcc12	ATP-binding cassette, sub-family C member 12	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20250821	MGI			PMID:33771553
1550860	Abcc12	ATP-binding cassette, sub-family C member 12	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20250821	MGI			PMID:33771553
1550860	Abcc12	ATP-binding cassette, sub-family C member 12	gene	MP:0009497	abnormal intrahepatic bile duct morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:33771553
1550860	Abcc12	ATP-binding cassette, sub-family C member 12	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20250821	MGI			PMID:33771553
1550860	Abcc12	ATP-binding cassette, sub-family C member 12	gene	MP:0012237	increased cholangiocyte apoptosis		IAGP		N	RGD:5509061	20250821	MGI			PMID:33771553
1550861	Plg	plasminogen	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9294211
1550861	Plg	plasminogen	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16554301
1550861	Plg	plasminogen	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20653841
1550861	Plg	plasminogen	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:15333838
1550861	Plg	plasminogen	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:20653841
1550861	Plg	plasminogen	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586361
1550861	Plg	plasminogen	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003846
1550861	Plg	plasminogen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20653841
1550861	Plg	plasminogen	gene	MP:0001139	abnormal vagina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9294211
1550861	Plg	plasminogen	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15333838
1550861	Plg	plasminogen	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586361
1550861	Plg	plasminogen	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417566
1550861	Plg	plasminogen	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
1550861	Plg	plasminogen	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671388
1550861	Plg	plasminogen	gene	MP:0001310	abnormal conjunctiva morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
1550861	Plg	plasminogen	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20653841
1550861	Plg	plasminogen	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8612226
1550861	Plg	plasminogen	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417566
1550861	Plg	plasminogen	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003846
1550861	Plg	plasminogen	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671388
1550861	Plg	plasminogen	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003846
1550861	Plg	plasminogen	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586361
1550861	Plg	plasminogen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
1550861	Plg	plasminogen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586361
1550861	Plg	plasminogen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9294211
1550861	Plg	plasminogen	gene	MP:0002249	abnormal larynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417566
1550861	Plg	plasminogen	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586361
1550861	Plg	plasminogen	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586361
1550861	Plg	plasminogen	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0003273	duodenal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0003282	gastric ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586361
1550861	Plg	plasminogen	gene	MP:0003282	gastric ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0003282	gastric ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0003300	gastrointestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0003305	proctitis		IAGP		N	RGD:5509061	20150702	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15333838
1550861	Plg	plasminogen	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20653841
1550861	Plg	plasminogen	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586361
1550861	Plg	plasminogen	gene	MP:0003434	decreased susceptibility to induced choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12657615
1550861	Plg	plasminogen	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373263
1550861	Plg	plasminogen	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9275201
1550861	Plg	plasminogen	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17301181
1550861	Plg	plasminogen	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
1550861	Plg	plasminogen	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17395831
1550861	Plg	plasminogen	gene	MP:0004481	abnormal conjunctival epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0004547	esophageal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0005035	perianal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0005035	perianal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:9294211
1550861	Plg	plasminogen	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557572
1550861	Plg	plasminogen	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7586361
1550861	Plg	plasminogen	gene	MP:0006137	venoocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0006164	ectropion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0006203	eye hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9473227
1550861	Plg	plasminogen	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003846
1550861	Plg	plasminogen	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003846
1550861	Plg	plasminogen	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17301181
1550861	Plg	plasminogen	gene	MP:0009507	abnormal mammary gland connective tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003846
1550861	Plg	plasminogen	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15333838
1550861	Plg	plasminogen	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373263
1550861	Plg	plasminogen	gene	MP:0010211	abnormal acute phase protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12657615
1550861	Plg	plasminogen	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11003846
1550861	Plg	plasminogen	gene	MP:0011507	abnormal kidney thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8929539
1550861	Plg	plasminogen	gene	MP:0012194	decreased keratinocyte migration		IAGP		N	RGD:5509061	20200625	MGI			PMID:7705657
1550861	Plg	plasminogen	gene	MP:0012331	increased circulating fibrinogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20653841
1550861	Plg	plasminogen	gene	MP:0020856	absent cornea epithelium		IAGP		N	RGD:5509061	20181101	MGI			PMID:9473227
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757825
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757825
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23253477
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23253477
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:23253477
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23253477
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0003410	abnormal artery development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757825
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23253477
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23253477
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757825
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23253477
1550862	Plekhg5	pleckstrin homology and RhoGEF domain containing G5	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757825
1550864	Cd300lb	CD300 molecule like family member B	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:20566714
1550865	Gapdhs	glyceraldehyde-3-phosphate dehydrogenase, spermatogenic	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:15546993
1550865	Gapdhs	glyceraldehyde-3-phosphate dehydrogenase, spermatogenic	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15546993
1550867	Kif26a	kinesin family member 26A	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0003289	abnormal intestinal peristalsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550867	Kif26a	kinesin family member 26A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914172
1550868	Ptpn7	protein tyrosine phosphatase, non-receptor type 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564869
1550871	Ift81	intraflagellar transport 81	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1550871	Ift81	intraflagellar transport 81	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1550871	Ift81	intraflagellar transport 81	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1550871	Ift81	intraflagellar transport 81	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
1550871	Ift81	intraflagellar transport 81	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1550871	Ift81	intraflagellar transport 81	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1550871	Ift81	intraflagellar transport 81	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550871	Ift81	intraflagellar transport 81	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20240613	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550871	Ift81	intraflagellar transport 81	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:32233951
1550874	Ncapg2	non-SMC condensin II complex, subunit G2	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20200310	MGI			PMID:14729962
1550874	Ncapg2	non-SMC condensin II complex, subunit G2	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14729962
1550874	Ncapg2	non-SMC condensin II complex, subunit G2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:14729962
1550874	Ncapg2	non-SMC condensin II complex, subunit G2	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:14729962
1550877	Dut	deoxyuridine triphosphatase	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:30987342
1550877	Dut	deoxyuridine triphosphatase	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20200806	MGI			PMID:30987342
1550877	Dut	deoxyuridine triphosphatase	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200806	MGI			PMID:30987342
1550880	Smap2	small ArfGAP 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20220922	MGI			PMID:26296315
1550880	Smap2	small ArfGAP 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20220922	MGI			PMID:26296315
1550880	Smap2	small ArfGAP 2	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0009377	ectopic manchette		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20220922	MGI			PMID:26296315
1550880	Smap2	small ArfGAP 2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20220922	MGI			PMID:26296315
1550880	Smap2	small ArfGAP 2	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550880	Smap2	small ArfGAP 2	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20220922	MGI			PMID:23864717
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550881	Pabpn1	poly(A) binding protein, nuclear 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20180201	MGI			PMID:28575395
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20241010	MGI			
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20241010	MGI			
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0002418	increased susceptibility to viral infection		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0002582	disorganized extraembryonic tissue		IEA		N	RGD:5509061	20241010	MGI			
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20241010	MGI			
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0009791	increased susceptibility to viral infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0010130	decreased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20210520	MGI			PMID:31427773
1550882	Snrnp40	small nuclear ribonucleoprotein 40 (U5)	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030629
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030629
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030629
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030629
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030629
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0010754	abnormal heart left ventricle pressure		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0020345	abnormal myocardial fiber currents		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0020419	decreased cardiac muscle relaxation		IAGP		N	RGD:5509061	20171026	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0031709	ventricular arrhythmia		IAGP		N	RGD:5509061	20260528	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0031711	monomorphic ventricular tachycardia		IAGP		N	RGD:5509061	20260528	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0031713	bidirectional ventricular tachycardia		IAGP		N	RGD:5509061	20260528	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0031734	doublet premature ventricular contraction		IAGP		N	RGD:5509061	20260716	MGI			PMID:28859293
1550883	Hrc	histidine rich calcium binding protein	gene	MP:0031736	ventricular bigeminy		IAGP		N	RGD:5509061	20260716	MGI			PMID:28859293
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20200310	MGI			PMID:24586561
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:24586561
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24586561
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:24586561
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20200514	MGI			
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20200514	MGI			
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20200310	MGI			PMID:24586561
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24586561
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24586561
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:24586561
1550884	Prepl	prolyl endopeptidase-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174946
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174946
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0004560	abnormal chorionic plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174946
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174946
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0009477	small cecum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21840293
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16983341
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174946
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:15964823
1550885	Spint1	serine protease inhibitor, Kunitz type 1	gene	MP:0030605	abnormal corneocyte morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:16983341
1550887	Mgp	matrix Gla protein	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12391016
1550887	Mgp	matrix Gla protein	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:12391016
1550887	Mgp	matrix Gla protein	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12391016
1550887	Mgp	matrix Gla protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0003211	abnormal aorta elastic fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0003279	aneurysm		IAGP		N	RGD:5509061	20200310	MGI			PMID:12391016
1550887	Mgp	matrix Gla protein	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0006093	arteriovenous malformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0006116	calcified aortic valve		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0006133	calcified artery		IAGP		N	RGD:5509061	20200310	MGI			PMID:12391016
1550887	Mgp	matrix Gla protein	gene	MP:0006133	calcified artery		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0006133	calcified artery		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0010480	pulmonary arteriovenous malformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0010522	calcified aorta		IAGP		N	RGD:5509061	20201112	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0010962	decreased compact bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0010988	abnormal bronchial cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9052783
1550887	Mgp	matrix Gla protein	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21765215
1550887	Mgp	matrix Gla protein	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550887	Mgp	matrix Gla protein	gene	MP:0030984	increased circulating osteocalcin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23994172
1550889	Plpp2	phospholipid phosphatase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10992322
1550897	Wdr44	WD repeat domain 44	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24252660
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24252660
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24252660
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24252660
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230119	MGI			
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24252660
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24252660
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24252660
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24252660
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24252660
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20230119	MGI			
1550898	Chd5	chromodomain helicase DNA binding protein 5	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:24252660
1550902	Arhgap8	Rho GTPase activating protein 8	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1550902	Arhgap8	Rho GTPase activating protein 8	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0000044	absent organ of Corti		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0000525	renal tubular acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0004403	absent cochlear outer hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1550903	Slc12a7	solute carrier family 12, member 7	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11976689
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0003865	lymph node inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0006173	abnormal myeloid dendritic cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0006412	abnormal T cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550908	Tnfaip8l2	tumor necrosis factor, alpha-induced protein 8-like 2	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:18455983
1550912	St7	suppression of tumorigenicity 7	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1550912	St7	suppression of tumorigenicity 7	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1550912	St7	suppression of tumorigenicity 7	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1550912	St7	suppression of tumorigenicity 7	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550912	St7	suppression of tumorigenicity 7	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1550915	Mrgpre	MAS-related GPR, member E	gene	MP:0003177	allodynia		IAGP		N	RGD:5509061	20150924	MGI			PMID:18197975
1550915	Mrgpre	MAS-related GPR, member E	gene	MP:0011436	decreased urine magnesium level		IEA		N	RGD:5509061	20211021	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20200514	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20200514	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20200514	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20241121	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210128	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20200514	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550917	Nsmce1	NSE1 homolog, SMC5-SMC6 complex component	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1550927	Git2	GIT ArfGAP 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715100
1550927	Git2	GIT ArfGAP 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715100
1550927	Git2	GIT ArfGAP 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715100
1550927	Git2	GIT ArfGAP 2	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1550927	Git2	GIT ArfGAP 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17565117
1550927	Git2	GIT ArfGAP 2	gene	MP:0002333	abnormal lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715100
1550927	Git2	GIT ArfGAP 2	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715100
1550927	Git2	GIT ArfGAP 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715100
1550927	Git2	GIT ArfGAP 2	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20431621
1550927	Git2	GIT ArfGAP 2	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20431621
1550927	Git2	GIT ArfGAP 2	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20431621
1550927	Git2	GIT ArfGAP 2	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715100
1550927	Git2	GIT ArfGAP 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20431621
1550927	Git2	GIT ArfGAP 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20431621
1550927	Git2	GIT ArfGAP 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20431621
1550927	Git2	GIT ArfGAP 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20431621
1550927	Git2	GIT ArfGAP 2	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715100
1550929	Phldb1	pleckstrin homology like domain, family B, member 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1550929	Phldb1	pleckstrin homology like domain, family B, member 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1550929	Phldb1	pleckstrin homology like domain, family B, member 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1550929	Phldb1	pleckstrin homology like domain, family B, member 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20231207	MGI			
1550929	Phldb1	pleckstrin homology like domain, family B, member 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1550929	Phldb1	pleckstrin homology like domain, family B, member 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1550929	Phldb1	pleckstrin homology like domain, family B, member 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200402	MGI			
1550931	Mapk15	mitogen-activated protein kinase 15	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1550931	Mapk15	mitogen-activated protein kinase 15	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20201022	MGI			
1550931	Mapk15	mitogen-activated protein kinase 15	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1550931	Mapk15	mitogen-activated protein kinase 15	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1550931	Mapk15	mitogen-activated protein kinase 15	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1550931	Mapk15	mitogen-activated protein kinase 15	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1550931	Mapk15	mitogen-activated protein kinase 15	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1550933	Laptm4a	lysosomal-associated protein transmembrane 4A	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1550933	Laptm4a	lysosomal-associated protein transmembrane 4A	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1550933	Laptm4a	lysosomal-associated protein transmembrane 4A	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20160421	MGI			
1550933	Laptm4a	lysosomal-associated protein transmembrane 4A	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20160421	MGI			
1550933	Laptm4a	lysosomal-associated protein transmembrane 4A	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1550934	Enc1	ectodermal-neural cortex 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1550934	Enc1	ectodermal-neural cortex 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1550934	Enc1	ectodermal-neural cortex 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1550934	Enc1	ectodermal-neural cortex 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1550934	Enc1	ectodermal-neural cortex 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1550934	Enc1	ectodermal-neural cortex 1	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20170105	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220428	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20240523	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0005376	homeostasis/metabolism phenotype		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0005397	hematopoietic system phenotype		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0005567	decreased circulating total protein level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0008805	decreased circulating amylase level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1550935	Wdr45	WD repeat domain 45	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0011897	decreased circulating unsaturated transferrin level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0013404	decreased circulating lactate level		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0020396	abnormal social recognition		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200130	MGI			PMID:26000824
1550935	Wdr45	WD repeat domain 45	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20210729	MGI			PMID:34043061
1550935	Wdr45	WD repeat domain 45	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:34043061
1550938	Tob2	transducer of ERBB2, 2	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18358842
1550938	Tob2	transducer of ERBB2, 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18358842
1550938	Tob2	transducer of ERBB2, 2	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18358842
1550938	Tob2	transducer of ERBB2, 2	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18358842
1550938	Tob2	transducer of ERBB2, 2	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18358842
1550938	Tob2	transducer of ERBB2, 2	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18358842
1550938	Tob2	transducer of ERBB2, 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18358842
1550939	Ticam2	TIR domain containing adaptor molecule 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14556004
1550939	Ticam2	TIR domain containing adaptor molecule 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IEA		N	RGD:5509061	20111116	MGI			
1550939	Ticam2	TIR domain containing adaptor molecule 2	gene	MP:0008658	decreased interleukin-1 beta secretion		IEA		N	RGD:5509061	20180215	MGI			
1550939	Ticam2	TIR domain containing adaptor molecule 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14556004
1550939	Ticam2	TIR domain containing adaptor molecule 2	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28592648
1550939	Ticam2	TIR domain containing adaptor molecule 2	gene	MP:0031704	decreased interferon type I secretion		IEA		N	RGD:5509061	20260402	MGI			
1550941	Nsmaf	neutral sphingomyelinase (N-SMase) activation associated factor	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228161
1550941	Nsmaf	neutral sphingomyelinase (N-SMase) activation associated factor	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:10228161
1550941	Nsmaf	neutral sphingomyelinase (N-SMase) activation associated factor	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:14985352
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20221103	MGI			
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20221103	MGI			
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20221103	MGI			
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20221103	MGI			
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0011078	increased macrophage cytokine production		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0012330	decreased circulating fibrinogen level		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0031083	increased circulating D-dimer level		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550942	Yod1	YOD1 deubiquitinase	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20241114	MGI			PMID:38789414
1550945	Phlpp1	PH domain and leucine rich repeat protein phosphatase 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1550945	Phlpp1	PH domain and leucine rich repeat protein phosphatase 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1550945	Phlpp1	PH domain and leucine rich repeat protein phosphatase 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
1550945	Phlpp1	PH domain and leucine rich repeat protein phosphatase 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
1550945	Phlpp1	PH domain and leucine rich repeat protein phosphatase 1	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26187040
1550945	Phlpp1	PH domain and leucine rich repeat protein phosphatase 1	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:26187040
1550945	Phlpp1	PH domain and leucine rich repeat protein phosphatase 1	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:20080691
1550945	Phlpp1	PH domain and leucine rich repeat protein phosphatase 1	gene	MP:0020475	delayed circadian behavior phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:20080691
1550946	Alkbh3	alkB homolog 3, alpha-ketoglutarate-dependent dioxygenase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16642038
1550946	Alkbh3	alkB homolog 3, alpha-ketoglutarate-dependent dioxygenase	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16642038
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0011246	abnormal fetal liver hematopoietic progenitor cell morphology		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0011695	absent hematopoietic stem cells		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550947	Zbtb11	zinc finger and BTB domain containing 11	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20250703	MGI			PMID:37567157
1550948	Uhmk1	U2AF homology motif (UHM) kinase 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:19033656
1550948	Uhmk1	U2AF homology motif (UHM) kinase 1	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:19033656
1550948	Uhmk1	U2AF homology motif (UHM) kinase 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:19033656
1550948	Uhmk1	U2AF homology motif (UHM) kinase 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19033656
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0001574	abnormal oxygen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0001942	abnormal lung volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20201022	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0003028	alkalosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0003032	hypocapnia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20231207	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0005573	increased pulmonary respiratory rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0005585	increased tidal volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:20399150
1550949	Hif1an	hypoxia-inducible factor 1, alpha subunit inhibitor	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:20399150
1550950	Rhbdl1	rhomboid like 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1550950	Rhbdl1	rhomboid like 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1550950	Rhbdl1	rhomboid like 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1550950	Rhbdl1	rhomboid like 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1550950	Rhbdl1	rhomboid like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1550950	Rhbdl1	rhomboid like 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1550951	Rnf141	ring finger protein 141	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23196134
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18064678
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18064678
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:18064678
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:22593209
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:18064678
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0004559	small allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18064678
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0008817	hematoma		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0010207	abnormal telomere morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18064678
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20220310	MGI			PMID:24115439
1550955	Rtel1	regulator of telomere elongation helicase 1	gene	MP:0030539	abnormal head paraxial mesoderm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15210109
1550957	Oxgr1	oxoglutarate (alpha-ketoglutarate) receptor 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23504326
1550957	Oxgr1	oxoglutarate (alpha-ketoglutarate) receptor 1	gene	MP:0003016	increased circulating bicarbonate level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23934124
1550957	Oxgr1	oxoglutarate (alpha-ketoglutarate) receptor 1	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23934124
1550957	Oxgr1	oxoglutarate (alpha-ketoglutarate) receptor 1	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20200310	MGI			PMID:23934124
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:25835743
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:7139332
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:9182797
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7139332
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9182797
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:7139332
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0001671	abnormal vitamin absorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:14517553
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:9182797
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002696	decreased circulating glucagon level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002715	decreased glycogen catabolism rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14517553
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9182797
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002883	chromatolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9182797
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:7139332
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:9182797
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20250508	MGI			
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20200310	MGI			PMID:25835743
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0011231	abnormal vitamin E level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:7139332
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:12788952
1550960	Pitpna	phosphatidylinositol transfer protein, alpha	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:12788952
1550963	Kcnq5	potassium voltage-gated channel, subfamily Q, member 5	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534576
1550963	Kcnq5	potassium voltage-gated channel, subfamily Q, member 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534576
1550965	Wdr47	WD repeat domain 47	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20200310	MGI			
1550965	Wdr47	WD repeat domain 47	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1550965	Wdr47	WD repeat domain 47	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20200310	MGI			
1550965	Wdr47	WD repeat domain 47	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20200310	MGI			
1550965	Wdr47	WD repeat domain 47	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20200310	MGI			
1550965	Wdr47	WD repeat domain 47	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200310	MGI			
1550965	Wdr47	WD repeat domain 47	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200310	MGI			
1550965	Wdr47	WD repeat domain 47	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20200310	MGI			
1550965	Wdr47	WD repeat domain 47	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1550966	Nova1	NOVA alternative splicing regulator 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719891
1550966	Nova1	NOVA alternative splicing regulator 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719891
1550966	Nova1	NOVA alternative splicing regulator 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719891
1550966	Nova1	NOVA alternative splicing regulator 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719891
1550966	Nova1	NOVA alternative splicing regulator 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719891
1550966	Nova1	NOVA alternative splicing regulator 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719891
1550966	Nova1	NOVA alternative splicing regulator 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719891
1550967	Hsd17b8	hydroxysteroid 17-beta dehydrogenase 8	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1550969	Sac3d1	SAC3 domain containing 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18838617
1550969	Sac3d1	SAC3 domain containing 1	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18838617
1550969	Sac3d1	SAC3 domain containing 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18838617
1550969	Sac3d1	SAC3 domain containing 1	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18838617
1550969	Sac3d1	SAC3 domain containing 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18838617
1550969	Sac3d1	SAC3 domain containing 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18838617
1550969	Sac3d1	SAC3 domain containing 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18838617
1550969	Sac3d1	SAC3 domain containing 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18838617
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0000928	incomplete rostral neuropore closure		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20210520	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0003400	kinked neural tube		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0013176	abnormal tail position or orientation		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0013177	abnormal tail tip morphology		IEA		N	RGD:5509061	20251204	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1550974	Ehbp1	EH domain binding protein 1	gene	MP:0014134	abnormal embryo morphology		IEA		N	RGD:5509061	20251204	MGI			
1550975	Gsdme	gasdermin E	gene	MP:0004401	increased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16023581
1550975	Gsdme	gasdermin E	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16023581
1550975	Gsdme	gasdermin E	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180920	MGI			PMID:28459430
1550975	Gsdme	gasdermin E	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20231207	MGI			
1550975	Gsdme	gasdermin E	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1550975	Gsdme	gasdermin E	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16804542
1550978	Tnfaip1	tumor necrosis factor, alpha-induced protein 1 (endothelial)	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1550978	Tnfaip1	tumor necrosis factor, alpha-induced protein 1 (endothelial)	gene	MP:0001391	abnormal tail movements		IEA		N	RGD:5509061	20160804	MGI			
1550978	Tnfaip1	tumor necrosis factor, alpha-induced protein 1 (endothelial)	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1550978	Tnfaip1	tumor necrosis factor, alpha-induced protein 1 (endothelial)	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1550978	Tnfaip1	tumor necrosis factor, alpha-induced protein 1 (endothelial)	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1550978	Tnfaip1	tumor necrosis factor, alpha-induced protein 1 (endothelial)	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20160804	MGI			
1550978	Tnfaip1	tumor necrosis factor, alpha-induced protein 1 (endothelial)	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160804	MGI			
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17438139
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0003624	anuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:25108225
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25108225
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25108225
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25108225
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0008137	absent podocytes		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20200310	MGI			PMID:25108225
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25108225
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17438139
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011455	absent glomerular endothelium fenestra		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011498	abnormal glomerular capsule parietal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011856	abnormal glomerular filtration barrier function		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011868	podocyte microvillus transformation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550979	Magi2	membrane associated guanylate kinase, WW and PDZ domain containing 2	gene	MP:0011871	podocyte hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25271328
1550980	Rbm3	RNA binding motif (RNP1, RRM) protein 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1550980	Rbm3	RNA binding motif (RNP1, RRM) protein 3	gene	MP:0002084	abnormal developmental patterning		IEA		N	RGD:5509061	20111116	MGI			
1550980	Rbm3	RNA binding motif (RNP1, RRM) protein 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21684257
1550980	Rbm3	RNA binding motif (RNP1, RRM) protein 3	gene	MP:0006386	absent somites		IEA		N	RGD:5509061	20111116	MGI			
1550980	Rbm3	RNA binding motif (RNP1, RRM) protein 3	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21684257
1550981	Omg	oligodendrocyte myelin glycoprotein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19672953
1550981	Omg	oligodendrocyte myelin glycoprotein	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18692574
1550982	Zfp111	zinc finger protein 111	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1550984	Mrgprb4	MAS-related GPR, member B4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618277
1550985	Pank4	pantothenate kinase 4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20231207	MGI			
1550985	Pank4	pantothenate kinase 4	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:30585370
1550985	Pank4	pantothenate kinase 4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20210318	MGI			PMID:30585370
1550985	Pank4	pantothenate kinase 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1550985	Pank4	pantothenate kinase 4	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20260402	MGI			
1550985	Pank4	pantothenate kinase 4	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:30585370
1550985	Pank4	pantothenate kinase 4	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:30585370
1550985	Pank4	pantothenate kinase 4	gene	MP:0008794	increased lens epithelium apoptosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30585370
1550985	Pank4	pantothenate kinase 4	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1550992	Usp5	ubiquitin specific peptidase 5 (isopeptidase T)	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20160114	MGI			
1550992	Usp5	ubiquitin specific peptidase 5 (isopeptidase T)	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1550992	Usp5	ubiquitin specific peptidase 5 (isopeptidase T)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1550993	Bcl7c	B cell CLL/lymphoma 7C	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1550994	Mpzl1	myelin protein zero-like 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1550994	Mpzl1	myelin protein zero-like 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20210311	MGI			PMID:32584792
1550994	Mpzl1	myelin protein zero-like 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20221215	MGI			
1550994	Mpzl1	myelin protein zero-like 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1551003	Tlr2	toll-like receptor 2	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0000181	abnormal circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656915
1551003	Tlr2	toll-like receptor 2	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656915
1551003	Tlr2	toll-like receptor 2	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980352
1551003	Tlr2	toll-like receptor 2	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408640
1551003	Tlr2	toll-like receptor 2	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118350
1551003	Tlr2	toll-like receptor 2	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534434
1551003	Tlr2	toll-like receptor 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211093
1551003	Tlr2	toll-like receptor 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250194
1551003	Tlr2	toll-like receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20171214	MGI			PMID:28769782
1551003	Tlr2	toll-like receptor 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408640
1551003	Tlr2	toll-like receptor 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403033
1551003	Tlr2	toll-like receptor 2	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998311
1551003	Tlr2	toll-like receptor 2	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0001652	colonic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475877
1551003	Tlr2	toll-like receptor 2	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17707128
1551003	Tlr2	toll-like receptor 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408640
1551003	Tlr2	toll-like receptor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843573
1551003	Tlr2	toll-like receptor 2	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626835
1551003	Tlr2	toll-like receptor 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1551003	Tlr2	toll-like receptor 2	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17704767
1551003	Tlr2	toll-like receptor 2	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244651
1551003	Tlr2	toll-like receptor 2	gene	MP:0002310	decreased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0002319	hyperoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244651
1551003	Tlr2	toll-like receptor 2	gene	MP:0002334	abnormal airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626835
1551003	Tlr2	toll-like receptor 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1551003	Tlr2	toll-like receptor 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751980
1551003	Tlr2	toll-like receptor 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091878
1551003	Tlr2	toll-like receptor 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690042
1551003	Tlr2	toll-like receptor 2	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751980
1551003	Tlr2	toll-like receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549626
1551003	Tlr2	toll-like receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1551003	Tlr2	toll-like receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751980
1551003	Tlr2	toll-like receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091878
1551003	Tlr2	toll-like receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690042
1551003	Tlr2	toll-like receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204620
1551003	Tlr2	toll-like receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118979
1551003	Tlr2	toll-like receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353199
1551003	Tlr2	toll-like receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998311
1551003	Tlr2	toll-like receptor 2	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091878
1551003	Tlr2	toll-like receptor 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0002738	hyperresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:17355971
1551003	Tlr2	toll-like receptor 2	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656915
1551003	Tlr2	toll-like receptor 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118350
1551003	Tlr2	toll-like receptor 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1551003	Tlr2	toll-like receptor 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118979
1551003	Tlr2	toll-like receptor 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353199
1551003	Tlr2	toll-like receptor 2	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21458307
1551003	Tlr2	toll-like receptor 2	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693552
1551003	Tlr2	toll-like receptor 2	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408640
1551003	Tlr2	toll-like receptor 2	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20171214	MGI			PMID:28769782
1551003	Tlr2	toll-like receptor 2	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509040
1551003	Tlr2	toll-like receptor 2	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17355971
1551003	Tlr2	toll-like receptor 2	gene	MP:0003916	decreased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656915
1551003	Tlr2	toll-like receptor 2	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:17355971
1551003	Tlr2	toll-like receptor 2	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509040
1551003	Tlr2	toll-like receptor 2	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17707128
1551003	Tlr2	toll-like receptor 2	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:16167081
1551003	Tlr2	toll-like receptor 2	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475853
1551003	Tlr2	toll-like receptor 2	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1551003	Tlr2	toll-like receptor 2	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135446
1551003	Tlr2	toll-like receptor 2	gene	MP:0005116	abnormal circulating pituitary hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211093
1551003	Tlr2	toll-like receptor 2	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1551003	Tlr2	toll-like receptor 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656915
1551003	Tlr2	toll-like receptor 2	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211093
1551003	Tlr2	toll-like receptor 2	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250194
1551003	Tlr2	toll-like receptor 2	gene	MP:0005345	abnormal circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20708624
1551003	Tlr2	toll-like receptor 2	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656915
1551003	Tlr2	toll-like receptor 2	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14656915
1551003	Tlr2	toll-like receptor 2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244651
1551003	Tlr2	toll-like receptor 2	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17548055
1551003	Tlr2	toll-like receptor 2	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693552
1551003	Tlr2	toll-like receptor 2	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17854911
1551003	Tlr2	toll-like receptor 2	gene	MP:0006080	brain ischemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19401158
1551003	Tlr2	toll-like receptor 2	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509040
1551003	Tlr2	toll-like receptor 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118979
1551003	Tlr2	toll-like receptor 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980352
1551003	Tlr2	toll-like receptor 2	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549626
1551003	Tlr2	toll-like receptor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1551003	Tlr2	toll-like receptor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12077222
1551003	Tlr2	toll-like receptor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16547271
1551003	Tlr2	toll-like receptor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250194
1551003	Tlr2	toll-like receptor 2	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980352
1551003	Tlr2	toll-like receptor 2	gene	MP:0008652	decreased interleukin-1 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16547271
1551003	Tlr2	toll-like receptor 2	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751980
1551003	Tlr2	toll-like receptor 2	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1551003	Tlr2	toll-like receptor 2	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1551003	Tlr2	toll-like receptor 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549626
1551003	Tlr2	toll-like receptor 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1551003	Tlr2	toll-like receptor 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751980
1551003	Tlr2	toll-like receptor 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739339
1551003	Tlr2	toll-like receptor 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1551003	Tlr2	toll-like receptor 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16547271
1551003	Tlr2	toll-like receptor 2	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739339
1551003	Tlr2	toll-like receptor 2	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244651
1551003	Tlr2	toll-like receptor 2	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1551003	Tlr2	toll-like receptor 2	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17707128
1551003	Tlr2	toll-like receptor 2	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118350
1551003	Tlr2	toll-like receptor 2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244651
1551003	Tlr2	toll-like receptor 2	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17355971
1551003	Tlr2	toll-like receptor 2	gene	MP:0009132	abnormal white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1551003	Tlr2	toll-like receptor 2	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20170803	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353199
1551003	Tlr2	toll-like receptor 2	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690042
1551003	Tlr2	toll-like receptor 2	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353199
1551003	Tlr2	toll-like receptor 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139201
1551003	Tlr2	toll-like receptor 2	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353199
1551003	Tlr2	toll-like receptor 2	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475877
1551003	Tlr2	toll-like receptor 2	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250194
1551003	Tlr2	toll-like receptor 2	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20708624
1551003	Tlr2	toll-like receptor 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17704767
1551003	Tlr2	toll-like receptor 2	gene	MP:0010266	decreased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19122641
1551003	Tlr2	toll-like receptor 2	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19122641
1551003	Tlr2	toll-like receptor 2	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20885960
1551003	Tlr2	toll-like receptor 2	gene	MP:0011077	decreased macrophage nitric oxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751980
1551003	Tlr2	toll-like receptor 2	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20141003	MGI			PMID:11751980
1551003	Tlr2	toll-like receptor 2	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546996
1551003	Tlr2	toll-like receptor 2	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0012320	abnormal body fat mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:19841034
1551003	Tlr2	toll-like receptor 2	gene	MP:0020449	decreased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:17355971
1551003	Tlr2	toll-like receptor 2	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171214	MGI			PMID:28769782
1551003	Tlr2	toll-like receptor 2	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20171214	MGI			PMID:28769782
1551003	Tlr2	toll-like receptor 2	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:14739339
1551003	Tlr2	toll-like receptor 2	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:20407745
1551003	Tlr2	toll-like receptor 2	gene	MP:0031025	decreased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:14739339
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679061
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556477
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679061
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556477
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679061
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556477
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679061
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556477
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679061
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716933
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679061
1551005	Mafg	Maf bZIP transcription factor G	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:10716933
1551006	Ltb	lymphotoxin B	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1551006	Ltb	lymphotoxin B	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1551006	Ltb	lymphotoxin B	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133428
1551006	Ltb	lymphotoxin B	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1551006	Ltb	lymphotoxin B	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436282
1551006	Ltb	lymphotoxin B	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133428
1551006	Ltb	lymphotoxin B	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133428
1551006	Ltb	lymphotoxin B	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133428
1551006	Ltb	lymphotoxin B	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133428
1551006	Ltb	lymphotoxin B	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1551006	Ltb	lymphotoxin B	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1551006	Ltb	lymphotoxin B	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1551006	Ltb	lymphotoxin B	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1551006	Ltb	lymphotoxin B	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133428
1551006	Ltb	lymphotoxin B	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1551006	Ltb	lymphotoxin B	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133428
1551006	Ltb	lymphotoxin B	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1551006	Ltb	lymphotoxin B	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1551006	Ltb	lymphotoxin B	gene	MP:0008179	absent germinal center B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1551006	Ltb	lymphotoxin B	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1551006	Ltb	lymphotoxin B	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436282
1551006	Ltb	lymphotoxin B	gene	MP:0008464	absent peripheral lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0008464	absent peripheral lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0008464	absent peripheral lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133428
1551006	Ltb	lymphotoxin B	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1551006	Ltb	lymphotoxin B	gene	MP:0008473	abnormal spleen follicular dendritic cell network		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1551006	Ltb	lymphotoxin B	gene	MP:0008473	abnormal spleen follicular dendritic cell network		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16705172
1551006	Ltb	lymphotoxin B	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1551006	Ltb	lymphotoxin B	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12354378
1551006	Ltb	lymphotoxin B	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436282
1551006	Ltb	lymphotoxin B	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436282
1551006	Ltb	lymphotoxin B	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1551006	Ltb	lymphotoxin B	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1551006	Ltb	lymphotoxin B	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1551006	Ltb	lymphotoxin B	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0009633	absent cervical lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0009633	absent cervical lymph nodes		IAGP		N	RGD:5509061	20170713	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10586051
1551006	Ltb	lymphotoxin B	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1551006	Ltb	lymphotoxin B	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446781
1551006	Ltb	lymphotoxin B	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256477
1551006	Ltb	lymphotoxin B	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12115620
1551006	Ltb	lymphotoxin B	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240709
1551006	Ltb	lymphotoxin B	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20226692
1551006	Ltb	lymphotoxin B	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:12446781
1551007	Ccl7	C-C motif chemokine ligand 7	gene	MP:0002620	abnormal monocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17364026
1551009	Map1lc3b	microtubule-associated protein 1 light chain 3 beta	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24185898
1551009	Map1lc3b	microtubule-associated protein 1 light chain 3 beta	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18069693
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19478059
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19478059
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20240523	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976163
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976163
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20200402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20200402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201231	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20241121	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20260402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976163
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20240523	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20240523	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20231207	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20210520	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19478059
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20260402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20240523	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20200402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20200402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19478059
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19478059
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004465	degeneration of organ of Corti supporting cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19478059
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19478059
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976163
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004774	abnormal bile salt level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976163
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210520	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976163
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976163
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20260402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20260402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20231207	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20200402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220519	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20150326	MGI			PMID:25068656
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210520	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:14976163
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220519	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20200402	MGI			
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19478059
1551010	Atp8b1	ATPase, class I, type 8B, member 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1551015	Exoc2	exocyst complex component 2	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191205	MGI			
1551015	Exoc2	exocyst complex component 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551015	Exoc2	exocyst complex component 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551015	Exoc2	exocyst complex component 2	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20240801	MGI			
1551016	Pcbd1	pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20200310	MGI			PMID:12011081
1551016	Pcbd1	pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12011081
1551016	Pcbd1	pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:12011081
1551016	Pcbd1	pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12011081
1551016	Pcbd1	pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1	gene	MP:0002893	ketoaciduria		IAGP		N	RGD:5509061	20200310	MGI			PMID:12011081
1551016	Pcbd1	pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12011081
1551016	Pcbd1	pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12011081
1551016	Pcbd1	pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1	gene	MP:0030670	increased circulating phenylalanine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12011081
1551017	Mypn	myopalladin	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1551017	Mypn	myopalladin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:28017374
1551017	Mypn	myopalladin	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1551017	Mypn	myopalladin	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20200310	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1551017	Mypn	myopalladin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28017374
1551017	Mypn	myopalladin	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20260618	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1551017	Mypn	myopalladin	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20200310	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0031730	atrial premature beat		IAGP		N	RGD:5509061	20260618	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0031744	shortened T wave		IAGP		N	RGD:5509061	20260716	MGI			PMID:25541130
1551017	Mypn	myopalladin	gene	MP:0031761	Mobitz II atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:25541130
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18307533
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18307533
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18307533
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18307533
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18307533
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18307533
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18307533
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18307533
1551018	Nuak2	NUAK family, SNF1-like kinase, 2	gene	MP:0012535	abnormal optic fissure closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22689267
1551020	Sv2c	synaptic vesicle glycoprotein 2c	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23458503
1551020	Sv2c	synaptic vesicle glycoprotein 2c	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23458503
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20200310	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201231	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20200310	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20200310	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20200310	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0005358	abnormal incisor morphology		IEA		N	RGD:5509061	20201022	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20220519	MGI			PMID:33961779
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1551023	Aff3	AF4/FMR2 family, member 3	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0001469	abnormal contextual conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060460
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060460
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347064
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060460
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347064
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060460
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060460
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060460
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060460
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060460
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347064
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347064
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060460
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20260402	MGI			
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0012453	decreased retrosplenial granular cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0012474	decreased cingulate cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0012478	decreased secondary somatosensory cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0020850	abnormal microtubule cytoskeleton morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:18347064
1551024	Ppp4c	protein phosphatase 4, catalytic subunit	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20220616	MGI			PMID:33543287
1551026	Dhrs1	dehydrogenase/reductase 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20240523	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20210128	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20241121	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200310	MGI			
1551029	Lpgat1	lysophosphatidylglycerol acyltransferase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:25954032
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:25954032
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:34318745
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:21124978
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:21124978
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21124978
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:21124978
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:25954032
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34318745
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0004716	abnormal cochlear nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0006392	abnormal nucleus pulposus morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34318745
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:21124978
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0008958	abnormal trophoblast glycogen cell morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0010038	abnormal placenta physiology		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0010503	myocardial trabeculae hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21124978
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011529	increased placenta intervillous maternal lacunae size		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0012726	abnormal uterine spiral artery morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0012727	abnormal uterine spiral artery remodeling		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:25954032
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0020452	abnormal axon radial sorting		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0030798	joint contracture		IAGP		N	RGD:5509061	20200310	MGI			PMID:21613327
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0030798	joint contracture		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0030802	abnormal tendon physiology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34318745
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0031418	increased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:24082093
1551030	Adgrg6	adhesion G protein-coupled receptor G6	gene	MP:0031607	abnormal fetal cardiomyocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:24082093
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0000362	decreased mast cell histamine storage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23103473
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0001619	abnormal vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20200702	MGI			PMID:28630327
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720327
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20200702	MGI			PMID:28630327
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23103473
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:28630327
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23103473
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20260402	MGI			
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16617107
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16617107
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0008020	abnormal dermal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:28630327
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200702	MGI			PMID:28630327
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23624557
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20200702	MGI			PMID:28630327
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0020449	decreased microglial cell activation		IAGP		N	RGD:5509061	20200702	MGI			PMID:28630327
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200702	MGI			PMID:28630327
1551031	Ptgdr	prostaglandin D receptor	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200702	MGI			PMID:28630327
1551032	Ypel2	yippee like 2	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1551032	Ypel2	yippee like 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220519	MGI			
1551032	Ypel2	yippee like 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1551032	Ypel2	yippee like 2	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20200514	MGI			
1551032	Ypel2	yippee like 2	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20220519	MGI			
1551032	Ypel2	yippee like 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1551032	Ypel2	yippee like 2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20200310	MGI			
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24599962
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:24599962
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24599962
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200310	MGI			
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24599962
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24599962
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220714	MGI			PMID:24599962
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20220714	MGI			PMID:24599962
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:24599962
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:24599962
1551033	Ddhd1	DDHD domain containing 1	gene	MP:0014464	decreased sperm mitochondrial sheath size		IAGP		N	RGD:5509061	20240613	MGI			PMID:24599962
1551036	Zgpat	zinc finger, CCCH-type with G patch domain	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1551036	Zgpat	zinc finger, CCCH-type with G patch domain	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1551040	Rundc3a	RUN domain containing 3A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1551040	Rundc3a	RUN domain containing 3A	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1551040	Rundc3a	RUN domain containing 3A	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1551040	Rundc3a	RUN domain containing 3A	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1551040	Rundc3a	RUN domain containing 3A	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1551040	Rundc3a	RUN domain containing 3A	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1551040	Rundc3a	RUN domain containing 3A	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1551040	Rundc3a	RUN domain containing 3A	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20250508	MGI			
1551043	Parp12	poly (ADP-ribose) polymerase family, member 12	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551043	Parp12	poly (ADP-ribose) polymerase family, member 12	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20200310	MGI			
1551043	Parp12	poly (ADP-ribose) polymerase family, member 12	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20200310	MGI			
1551043	Parp12	poly (ADP-ribose) polymerase family, member 12	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1551043	Parp12	poly (ADP-ribose) polymerase family, member 12	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1551043	Parp12	poly (ADP-ribose) polymerase family, member 12	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551043	Parp12	poly (ADP-ribose) polymerase family, member 12	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1551043	Parp12	poly (ADP-ribose) polymerase family, member 12	gene	MP:0005573	increased pulmonary respiratory rate		IEA		N	RGD:5509061	20201022	MGI			
1551043	Parp12	poly (ADP-ribose) polymerase family, member 12	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1551044	Phf7	PHD finger protein 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210429	MGI			PMID:32726616
1551044	Phf7	PHD finger protein 7	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210429	MGI			PMID:32726616
1551044	Phf7	PHD finger protein 7	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20210429	MGI			PMID:32726616
1551044	Phf7	PHD finger protein 7	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210429	MGI			PMID:32726616
1551044	Phf7	PHD finger protein 7	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20210429	MGI			PMID:32726616
1551044	Phf7	PHD finger protein 7	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32726616
1551044	Phf7	PHD finger protein 7	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32726616
1551044	Phf7	PHD finger protein 7	gene	MP:0009233	enlarged sperm head		IAGP		N	RGD:5509061	20210429	MGI			PMID:32726616
1551044	Phf7	PHD finger protein 7	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20210429	MGI			PMID:32726616
1551044	Phf7	PHD finger protein 7	gene	MP:0011972	decreased circulating lactate dehydrogenase level		IEA		N	RGD:5509061	20250508	MGI			
1551046	Gpr50	G-protein-coupled receptor 50	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17957037
1551046	Gpr50	G-protein-coupled receptor 50	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17957037
1551046	Gpr50	G-protein-coupled receptor 50	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17957037
1551046	Gpr50	G-protein-coupled receptor 50	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17957037
1551046	Gpr50	G-protein-coupled receptor 50	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17957037
1551046	Gpr50	G-protein-coupled receptor 50	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17957037
1551046	Gpr50	G-protein-coupled receptor 50	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17957037
1551046	Gpr50	G-protein-coupled receptor 50	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17957037
1551047	Akap8l	A kinase anchor protein 8-like	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1551047	Akap8l	A kinase anchor protein 8-like	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000322	increased granulocyte number		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000384	distorted hair follicle pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000384	distorted hair follicle pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001256	abnormal body length		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0003062	abnormal coping response		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0008211	decreased mature B cell number		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0008501	increased IgG2b level		IEA		N	RGD:5509061	20200310	MGI			
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22169041
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0011277	decreased tail pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551048	Mysm1	myb-like, SWIRM and MPN domains 1	gene	MP:0011277	decreased tail pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551049	Zbtb40	zinc finger and BTB domain containing 40	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20201015	MGI			PMID:32497039
1551049	Zbtb40	zinc finger and BTB domain containing 40	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20201015	MGI			PMID:32497039
1551049	Zbtb40	zinc finger and BTB domain containing 40	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20201015	MGI			PMID:32497039
1551049	Zbtb40	zinc finger and BTB domain containing 40	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20201015	MGI			PMID:32497039
1551049	Zbtb40	zinc finger and BTB domain containing 40	gene	MP:0011585	decreased alkaline phosphatase activity		IAGP		N	RGD:5509061	20201015	MGI			PMID:32497039
1551049	Zbtb40	zinc finger and BTB domain containing 40	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20201015	MGI			PMID:32497039
1551049	Zbtb40	zinc finger and BTB domain containing 40	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20201015	MGI			PMID:32497039
1551049	Zbtb40	zinc finger and BTB domain containing 40	gene	MP:0021190	decreased bone mineral density of lumbar vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:32497039
1551051	Lct	lactase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1551051	Lct	lactase	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0001460	abnormal olfactory discrimination memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0002856	abnormal vestibular ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0003686	abnormal eye muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0004081	abnormal globus pallidus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0004292	abnormal spiral ligament fibrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0008265	abnormal hippocampus CA2 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16014715
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551052	Man2b1	mannosidase 2, alpha B1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10400983
1551053	Zfp318	zinc finger protein 318	gene	MP:0001922	reduced male fertility		IEA		N	RGD:5509061	20141003	MGI			
1551053	Zfp318	zinc finger protein 318	gene	MP:0002458	abnormal B cell number		IEA		N	RGD:5509061	20141003	MGI			
1551053	Zfp318	zinc finger protein 318	gene	MP:0002491	decreased IgD level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24616512
1551053	Zfp318	zinc finger protein 318	gene	MP:0002491	decreased IgD level		IAGP		N	RGD:5509061	20141225	MGI			PMID:25057009
1551053	Zfp318	zinc finger protein 318	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24616512
1551053	Zfp318	zinc finger protein 318	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141225	MGI			PMID:25057009
1551053	Zfp318	zinc finger protein 318	gene	MP:0008191	abnormal follicular B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24616512
1551053	Zfp318	zinc finger protein 318	gene	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24616512
1551053	Zfp318	zinc finger protein 318	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24616512
1551053	Zfp318	zinc finger protein 318	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141225	MGI			PMID:25057009
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0000032	cochlear degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22330676
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22330676
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0000048	abnormal stria vascularis morphology		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1728569
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4067076
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6541219
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7093705
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7432512
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7719036
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648588
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1728569
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6541219
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6662828
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7432512
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7719036
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0002857	cochlear ganglion degeneration		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0002894	abnormal otolith morphology		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0003149	abnormal tectorial membrane morphology		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0003169	abnormal scala media morphology		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0003879	abnormal hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004300	abnormal organ of Corti supporting cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22330676
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004302	abnormal Deiters cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22330676
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004331	vestibular saccular macula degeneration		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22330676
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22330676
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004432	abnormal cochlear hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22330676
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004628	Deiters cell degeneration		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:16648588
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0005307	head tossing		IEA		N	RGD:5509061	20111116	MGI			
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22330676
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0011039	abnormal vestibuloocular dark reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551056	Tmc1	transmembrane channel-like gene family 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22105175
1551060	Aaas	achalasia, adrenocortical insufficiency, alacrimia	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16479006
1551060	Aaas	achalasia, adrenocortical insufficiency, alacrimia	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16479006
1551060	Aaas	achalasia, adrenocortical insufficiency, alacrimia	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16479006
1551060	Aaas	achalasia, adrenocortical insufficiency, alacrimia	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16479006
1551060	Aaas	achalasia, adrenocortical insufficiency, alacrimia	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16479006
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210826	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20150430	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210826	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0008177	increased germinal center B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1551061	Ydjc	YdjC homolog (bacterial)	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0000315	hemoglobinuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733003
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733003
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733003
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733003
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0004882	enlarged lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005139	increased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491259
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733003
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20733003
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0011567	increased renal glomerulus lobularity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11287624
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:17372192
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:20733003
1551063	Mark2	MAP/microtubule affinity regulating kinase 2	gene	MP:0031270	decreased susceptibility to age-related hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:17372192
1551064	Ube4a	ubiquitination factor E4A	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1551064	Ube4a	ubiquitination factor E4A	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210520	MGI			
1551064	Ube4a	ubiquitination factor E4A	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1551064	Ube4a	ubiquitination factor E4A	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20220519	MGI			
1551064	Ube4a	ubiquitination factor E4A	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1551064	Ube4a	ubiquitination factor E4A	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210520	MGI			
1551064	Ube4a	ubiquitination factor E4A	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210520	MGI			
1551064	Ube4a	ubiquitination factor E4A	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1551067	Mlycd	malonyl-CoA decarboxylase	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030679
1551067	Mlycd	malonyl-CoA decarboxylase	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030679
1551067	Mlycd	malonyl-CoA decarboxylase	gene	MP:0015001	increased glucose oxidation		IAGP		N	RGD:5509061	20260611	MGI			PMID:17030679
1551071	Prokr1	prokineticin receptor 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18421008
1551071	Prokr1	prokineticin receptor 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220519	MGI			
1551071	Prokr1	prokineticin receptor 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18421008
1551071	Prokr1	prokineticin receptor 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16793879
1551071	Prokr1	prokineticin receptor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16537498
1551071	Prokr1	prokineticin receptor 1	gene	MP:0002733	abnormal thermal nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:16793879
1551071	Prokr1	prokineticin receptor 1	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16793879
1551071	Prokr1	prokineticin receptor 1	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16793879
1551071	Prokr1	prokineticin receptor 1	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:16793879
1551071	Prokr1	prokineticin receptor 1	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:16793879
1551071	Prokr1	prokineticin receptor 1	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16793879
1551071	Prokr1	prokineticin receptor 1	gene	MP:0011947	abnormal fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16793879
1551071	Prokr1	prokineticin receptor 1	gene	MP:0020329	decreased capillary density		IAGP		N	RGD:5509061	20160714	MGI			PMID:18421008
1551072	Ctrb1	chymotrypsinogen B1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200924	MGI			PMID:30076839
1551072	Ctrb1	chymotrypsinogen B1	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20200924	MGI			PMID:32678161
1551072	Ctrb1	chymotrypsinogen B1	gene	MP:0003450	enlarged pancreas		IAGP		N	RGD:5509061	20200924	MGI			PMID:30076839
1551072	Ctrb1	chymotrypsinogen B1	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20200924	MGI			PMID:30076839
1551072	Ctrb1	chymotrypsinogen B1	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20200924	MGI			PMID:32678161
1551072	Ctrb1	chymotrypsinogen B1	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20200924	MGI			PMID:30076839
1551074	Lingo2	leucine rich repeat and Ig domain containing 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1551074	Lingo2	leucine rich repeat and Ig domain containing 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230601	MGI			
1551074	Lingo2	leucine rich repeat and Ig domain containing 2	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20230601	MGI			
1551074	Lingo2	leucine rich repeat and Ig domain containing 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1551074	Lingo2	leucine rich repeat and Ig domain containing 2	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20230601	MGI			
1551074	Lingo2	leucine rich repeat and Ig domain containing 2	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230601	MGI			
1551074	Lingo2	leucine rich repeat and Ig domain containing 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1551074	Lingo2	leucine rich repeat and Ig domain containing 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1551080	Ccl22	C-C motif chemokine ligand 22	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20170615	MGI			PMID:27195186
1551080	Ccl22	C-C motif chemokine ligand 22	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20111116	MGI			
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20111116	MGI			
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0001264	increased body size		IEA		N	RGD:5509061	20111116	MGI			
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0001565	abnormal circulating phosphate level		IEA		N	RGD:5509061	20111116	MGI			
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0008597	decreased circulating interleukin-6 level		IEA		N	RGD:5509061	20111116	MGI			
1551081	Txndc2	thioredoxin domain containing 2 (spermatozoa)	gene	MP:0012582	increased peroxidase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0000381	enlarged hair follicles		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101409
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23755247
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23755247
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001320	small pupil		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18983969
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23755247
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0002274	abnormal type I pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0002579	disorganized secondary lens fibers		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:20980403
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18983969
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0003092	decreased cornea stroma thickness		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23755247
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0003671	abnormal eyelid aperture		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20980403
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0004481	abnormal conjunctival epithelium morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101409
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18395082
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101409
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0004962	decreased prostate gland weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23755247
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18395082
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18983969
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005247	abnormal extraocular muscle morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005573	increased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101409
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101409
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0006167	eyelid edema		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101409
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20181011	MGI			
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0009381	abnormal prostate gland dorsolateral lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23755247
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0009662	abnormal uterine receptivity		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0009666	abnormal embryo attachment		IAGP		N	RGD:5509061	20220303	MGI			PMID:22233806
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0009742	increased cornea stroma thickness		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101409
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0009935	abnormal Meibomian gland acinus morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0010814	absent alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0010816	decreased type I pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0010894	pulmonary alveolar edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101409
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18983969
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20980403
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599506
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0011163	increased wet-to-dry lung weight ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:20038803
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0011482	posterior iris synechia		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20980403
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0012117	decreased trophectoderm cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20980403
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0013385	abnormal Meibomian gland development		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0013391	abnormal Meibomian gland physiology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0013394	abnormal palpebral conjunctiva morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0013527	absent conjunctiva goblet cells		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0013754	abnormal ocular surface morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0014147	lacrimal gland necrosis		IAGP		N	RGD:5509061	20160407	MGI			PMID:21600198
1551083	Klf5	Kruppel-like transcription factor 5	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:21600198
1551084	Zbp1	Z-DNA binding protein 1	gene	MP:0012555	decreased cell death		IAGP		N	RGD:5509061	20180125	MGI			PMID:28716805
1551084	Zbp1	Z-DNA binding protein 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1551084	Zbp1	Z-DNA binding protein 1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28716805
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551086	Camta1	calmodulin binding transcription activator 1	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25049392
1551089	Cmpk1	cytidine/uridine monophosphate kinase 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1551089	Cmpk1	cytidine/uridine monophosphate kinase 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20200310	MGI			
1551089	Cmpk1	cytidine/uridine monophosphate kinase 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1551089	Cmpk1	cytidine/uridine monophosphate kinase 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1551089	Cmpk1	cytidine/uridine monophosphate kinase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551092	Ctu2	cytosolic thiouridylase subunit 2	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551092	Ctu2	cytosolic thiouridylase subunit 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551092	Ctu2	cytosolic thiouridylase subunit 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230413	MGI			PMID:36087511
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260430	MGI			PMID:38099646
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230413	MGI			PMID:36087511
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20260430	MGI			PMID:38099646
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26808229
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26808229
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20201022	MGI			
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26808229
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0008087	decreased T helper 1 cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26808229
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0008462	abnormal medium spiny neuron morphology		IAGP		N	RGD:5509061	20260430	MGI			PMID:38099646
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26808229
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0008615	decreased circulating interleukin-17 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26808229
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20260430	MGI			PMID:38099646
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0010220	decreased T-helper 17 cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26808229
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20260430	MGI			PMID:38099646
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20230413	MGI			PMID:36087511
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:36087511
1551093	Zranb1	zinc finger, RAN-binding domain containing 1	gene	MP:0014219	decreased intestinal mucosa thickness		IAGP		N	RGD:5509061	20230413	MGI			PMID:36087511
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7603567
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000384	distorted hair follicle pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160181
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17096024
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9120401
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9120401
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299349
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433815
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001220	epidermal necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7603567
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9120401
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525802
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525802
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19263497
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160181
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0002814	hyperchromasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7603567
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433815
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003303	peritoneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160181
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160181
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525802
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16485035
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7603567
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17096024
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9120401
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10433815
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160181
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9120401
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9120401
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9120401
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008112	abnormal monocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11869686
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11869686
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11034607
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008343	abnormal gamma-delta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9120401
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606991
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525802
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525802
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299349
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0009405	increased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299349
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11160181
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525802
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250470
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0010170	abnormal glial cell apoptosis		IAGP		N	RGD:5509061	20251204	MGI			PMID:15905096
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10702415
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518539
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17101783
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7603567
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9120401
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18408078
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17101783
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:10518539
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0020854	increased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:20713516
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0030582	abnormal hair follicle placode formation		IAGP		N	RGD:5509061	20180614	MGI			PMID:15199130
1551095	Rela	Rela proto-oncogene, NFKB subunit	gene	MP:0031319	impaired intestine regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:18250470
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408640
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456769
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17357057
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17707128
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626835
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002334	abnormal airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626835
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447442
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486093
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21760953
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23334413
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20200423	MGI			PMID:19079579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002421	abnormal cell-mediated immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447442
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800576
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447442
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872135
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118979
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776906
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21760953
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158234
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16703567
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23334413
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16703567
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15034168
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17118979
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855887
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20200423	MGI			PMID:19079579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21458307
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17408640
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19218085
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17591966
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475853
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0004242	abnormal plasmacytoid dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723216
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20526283
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668221
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16440059
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16703567
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456769
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135446
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12447442
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20150305	MGI			PMID:24439266
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20150305	MGI			PMID:24439266
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244651
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981228
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0006334	abnormal susceptibility to hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17357057
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20150305	MGI			PMID:24439266
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135446
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16703567
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16703567
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20530205
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855887
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18641654
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872135
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135446
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456769
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800576
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17723216
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20200423	MGI			PMID:16985170
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135446
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23334413
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407889
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135446
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17456769
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17525287
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855887
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21760953
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244651
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18776906
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204620
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17707128
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20220616	MGI			PMID:33343574
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244651
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855887
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20530205
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0008906	abnormal parametrial fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21804564
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17704767
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20210204	MGI			PMID:22586041
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010222	abnormal T-helper 17 cell physiology		IAGP		N	RGD:5509061	20150305	MGI			PMID:24439266
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010266	decreased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204620
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998396
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010750	increased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18656388
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:23179078
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0011077	decreased macrophage nitric oxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808018
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:21804564
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0020186	abnormal susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22851711
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:14993594
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16832055
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:15800576
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16625202
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:19079579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:19079579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200702	MGI			PMID:26136579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0031054	bronchiolitis		IAGP		N	RGD:5509061	20200709	MGI			PMID:19079579
1551097	Myd88	myeloid differentiation primary response gene 88	gene	MP:0031225	decreased CXCL10 level		IAGP		N	RGD:5509061	20210204	MGI			PMID:22586041
1551102	Bpi	bactericidal permeablility increasing protein	gene	MP:0001819	abnormal immune cell physiology		IAGP		N	RGD:5509061	20240509	MGI			PMID:38457343
1551102	Bpi	bactericidal permeablility increasing protein	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20240509	MGI			PMID:38457343
1551102	Bpi	bactericidal permeablility increasing protein	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20240509	MGI			PMID:38457343
1551102	Bpi	bactericidal permeablility increasing protein	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20240509	MGI			PMID:38457343
1551102	Bpi	bactericidal permeablility increasing protein	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20240509	MGI			PMID:38457343
1551102	Bpi	bactericidal permeablility increasing protein	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20240509	MGI			PMID:38457343
1551102	Bpi	bactericidal permeablility increasing protein	gene	MP:0008588	abnormal circulating interleukin level		IAGP		N	RGD:5509061	20240509	MGI			PMID:38457343
1551103	Slc5a11	solute carrier family 5 (sodium/glucose cotransporter), member 11	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1551103	Slc5a11	solute carrier family 5 (sodium/glucose cotransporter), member 11	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0002450	abnormal lymph organ development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0010426	abnormal heart and great artery attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0010439	abnormal hepatic vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0010912	herniated liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0012269	nuchal edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538705
1551104	Nprl3	nitrogen permease regulator-like 3	gene	MP:0014519	myocardial ventricular hypertrabeculation		IAGP		N	RGD:5509061	20240822	MGI			PMID:22538705
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20170105	MGI			
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20170105	MGI			
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794888
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794888
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794888
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201022	MGI			
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:18794888
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0003064	decreased coping response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794888
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0003459	increased fear-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794888
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794888
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20170105	MGI			
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794888
1551107	Slitrk1	SLIT and NTRK-like family, member 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794888
1551109	Smpdl3a	sphingomyelin phosphodiesterase, acid-like 3A	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1551109	Smpdl3a	sphingomyelin phosphodiesterase, acid-like 3A	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8096198
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8096198
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8096198
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978099
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8096198
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978099
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978099
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978099
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8096198
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8096198
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8096198
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978099
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8096198
1551110	Pou2f2	POU domain, class 2, transcription factor 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1551114	Calcoco1	calcium binding and coiled coil domain 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20241121	MGI			
1551114	Calcoco1	calcium binding and coiled coil domain 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20240523	MGI			
1551114	Calcoco1	calcium binding and coiled coil domain 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220519	MGI			
1551114	Calcoco1	calcium binding and coiled coil domain 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210826	MGI			
1551114	Calcoco1	calcium binding and coiled coil domain 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20201022	MGI			
1551114	Calcoco1	calcium binding and coiled coil domain 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20210826	MGI			
1551114	Calcoco1	calcium binding and coiled coil domain 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1551114	Calcoco1	calcium binding and coiled coil domain 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1551114	Calcoco1	calcium binding and coiled coil domain 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1551117	Zfp407	zinc finger protein 407	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1551117	Zfp407	zinc finger protein 407	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20240926	MGI			
1551117	Zfp407	zinc finger protein 407	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20201022	MGI			
1551117	Zfp407	zinc finger protein 407	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191205	MGI			
1551117	Zfp407	zinc finger protein 407	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20191205	MGI			
1551117	Zfp407	zinc finger protein 407	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551117	Zfp407	zinc finger protein 407	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20191205	MGI			
1551117	Zfp407	zinc finger protein 407	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551119	Ttc9	tetratricopeptide repeat domain 9	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20200310	MGI			PMID:25798063
1551119	Ttc9	tetratricopeptide repeat domain 9	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25798063
1551119	Ttc9	tetratricopeptide repeat domain 9	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:25798063
1551119	Ttc9	tetratricopeptide repeat domain 9	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:25798063
1551119	Ttc9	tetratricopeptide repeat domain 9	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:25798063
1551120	Rbm19	RNA binding motif protein 19	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:19087264
1551120	Rbm19	RNA binding motif protein 19	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19087264
1551120	Rbm19	RNA binding motif protein 19	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19087264
1551120	Rbm19	RNA binding motif protein 19	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19087264
1551120	Rbm19	RNA binding motif protein 19	gene	MP:0012111	failure of morula compaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:19087264
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490740
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171887
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490740
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:18490740
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490740
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490740
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490740
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0005398	decreased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171887
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490740
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490740
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171887
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008615	decreased circulating interleukin-17 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171887
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008680	abnormal interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171887
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171887
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551121	Clec4e	C-type lectin domain family 4, member e	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1551124	Cab39l	calcium binding protein 39-like	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20200310	MGI			
1551124	Cab39l	calcium binding protein 39-like	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38676926
1551124	Cab39l	calcium binding protein 39-like	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1551124	Cab39l	calcium binding protein 39-like	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240801	MGI			PMID:38676926
1551126	Rbm26	RNA binding motif protein 26	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940672
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940672
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940672
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672719
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940672
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0001717	absent ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672719
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672719
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857798
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940672
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940672
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940672
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940672
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672719
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0011200	abnormal extraembryonic coelom morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551127	Tfap2c	transcription factor AP-2, gamma	gene	MP:0011207	absent ectoplacental cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015300
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20141003	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20141003	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20170105	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000678	abnormal parathyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21357625
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0001562	abnormal circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002249	abnormal larynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482476
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21357625
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689889
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20141003	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20170105	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002876	abnormal thyroid gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002905	decreased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0002985	abnormal urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171764
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210128	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0003996	clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847339
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689889
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20170105	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0004697	abnormal thyroid follicular cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084302
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20161027	MGI			PMID:26168216
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20141003	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199583
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005406	abnormal heart size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17694176
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20161027	MGI			PMID:26168216
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19171764
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20141003	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21357625
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0010326	malleus hypoplasia		IAGP		N	RGD:5509061	20170928	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0010640	ventricular myocardium compact layer hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689889
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0012045	increased susceptibility to hypertension		IAGP		N	RGD:5509061	20161027	MGI			PMID:26168216
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20191128	MGI			PMID:28194446
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0020106	decreased nitrate level		IAGP		N	RGD:5509061	20161027	MGI			PMID:26168216
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:16988000
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0030107	incus hypoplasia		IAGP		N	RGD:5509061	20170928	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0030128	stapes hypoplasia		IAGP		N	RGD:5509061	20170928	MGI			PMID:9687499
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0030299	lower jaw to upper jaw transformation		IAGP		N	RGD:5509061	20171102	MGI			PMID:18199583
1551128	Gna11	guanine nucleotide binding protein, alpha 11	gene	MP:0030884	rachitic rosary		IAGP		N	RGD:5509061	20181101	MGI			PMID:16988000
1551129	Lman2	lectin, mannose-binding 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1551129	Lman2	lectin, mannose-binding 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1551130	Atp6v1g2	ATPase, H+ transporting, lysosomal V1 subunit G2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0009837	abnormal sperm end piece morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20200310	MGI			PMID:30929735
1551133	Ttc21a	tetratricopeptide repeat domain 21A	gene	MP:0031352	absent sperm axonemal central pair		IAGP		N	RGD:5509061	20220811	MGI			PMID:30929735
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0010751	decreased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0011236	increased blood oxygen capacity		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0011913	abnormal reticulocyte cell number		IAGP		N	RGD:5509061	20210304	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0014990	enhanced erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:32966787
1551134	Bpgm	2,3-bisphosphoglycerate mutase	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20210805	MGI			PMID:32966787
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201231	MGI			
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20181227	MGI			
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160421	MGI			
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20170105	MGI			
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20160421	MGI			
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20240613	MGI			PMID:29101251
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20240613	MGI			PMID:29101251
1551135	Nsd3	nuclear receptor binding SET domain protein 3	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240613	MGI			PMID:29101251
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20190221	MGI			PMID:24814481
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20190221	MGI			PMID:24814481
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20190221	MGI			PMID:24814481
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20190221	MGI			PMID:24814481
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20190221	MGI			PMID:24814481
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0014173	increased fatty acid beta-oxidation		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0014574	decreased circulating resistin level		IAGP		N	RGD:5509061	20241128	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0020521	browned white adipose tissue morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20190228	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:26997277
1551139	Abhd6	abhydrolase domain containing 6	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:26997277
1551140	Marchf7	membrane associated ring-CH-type finger 7	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15670816
1551140	Marchf7	membrane associated ring-CH-type finger 7	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15670816
1551140	Marchf7	membrane associated ring-CH-type finger 7	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:15670816
1551140	Marchf7	membrane associated ring-CH-type finger 7	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15670816
1551140	Marchf7	membrane associated ring-CH-type finger 7	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15670816
1551140	Marchf7	membrane associated ring-CH-type finger 7	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15670816
1551140	Marchf7	membrane associated ring-CH-type finger 7	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15670816
1551141	Cryba2	crystallin, beta A2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212184
1551141	Cryba2	crystallin, beta A2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212184
1551141	Cryba2	crystallin, beta A2	gene	MP:0010251	subcapsular cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212184
1551141	Cryba2	crystallin, beta A2	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:21212184
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687236
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196176
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:22370636
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23873941
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:23873941
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540175
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196176
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196176
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687236
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540175
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196176
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540175
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713620
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597047
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597047
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687236
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687236
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597047
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540175
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687236
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004834	ovary hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687236
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597047
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15713620
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060635
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594509
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22722829
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0006422	increased mammary adenoacanthoma incidence		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:25742742
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540175
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0008940	delayed balanopreputial separation		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0009216	abnormal peritoneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18594509
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0009469	increased skin hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23873941
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0009715	thick epidermis stratum basale		IAGP		N	RGD:5509061	20141003	MGI			PMID:23873941
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0009819	abnormal circulating androgen level		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20220317	MGI			PMID:28357399
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0010173	increased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540175
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22370636
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0010364	increased fibroadenoma incidence		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597047
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540175
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540175
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10196176
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15687236
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625210
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540175
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200109	MGI			PMID:25742742
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0012732	abnormal perineural vascular plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18449193
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:22214849
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0013778	abnormal mammary gland myoepithelium morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0013782	abnormal mammary duct terminal end bud morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551142	Pik3ca	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	gene	MP:0014057	abnormal mammary gland stroma morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:22666336
1551143	Phkg1	phosphorylase kinase gamma 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220519	MGI			
1551143	Phkg1	phosphorylase kinase gamma 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20220519	MGI			
1551143	Phkg1	phosphorylase kinase gamma 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220519	MGI			
1551143	Phkg1	phosphorylase kinase gamma 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220519	MGI			
1551143	Phkg1	phosphorylase kinase gamma 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220519	MGI			
1551143	Phkg1	phosphorylase kinase gamma 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1551143	Phkg1	phosphorylase kinase gamma 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20220519	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037259
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037259
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000960	abnormal sensory ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037259
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20250508	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0001393	ataxia		IEA		N	RGD:5509061	20111116	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20250508	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037259
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0001785	edema		IEA		N	RGD:5509061	20260402	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037259
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20260402	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20260402	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0002183	gliosis		IEA		N	RGD:5509061	20111116	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037259
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23047693
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037259
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20260402	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037259
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19037259
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0012503	increased midbrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0020851	abnormal vacuole morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:17956977
1551146	Vac14	Vac14 homolog (S. cerevisiae)	gene	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:17956977
1551147	Lama5	laminin, alpha 5	gene	MP:0000024	lowered ear position		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0000075	absent neurocranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20220428	MGI			PMID:28735299
1551147	Lama5	laminin, alpha 5	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12921739
1551147	Lama5	laminin, alpha 5	gene	MP:0000484	abnormal pulmonary artery morphology		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12921739
1551147	Lama5	laminin, alpha 5	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:28735299
1551147	Lama5	laminin, alpha 5	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10625553
1551147	Lama5	laminin, alpha 5	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10625553
1551147	Lama5	laminin, alpha 5	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0000650	mesocardia		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1551147	Lama5	laminin, alpha 5	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1551147	Lama5	laminin, alpha 5	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1551147	Lama5	laminin, alpha 5	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1551147	Lama5	laminin, alpha 5	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0001697	abnormal embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1551147	Lama5	laminin, alpha 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847204
1551147	Lama5	laminin, alpha 5	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10625553
1551147	Lama5	laminin, alpha 5	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12051813
1551147	Lama5	laminin, alpha 5	gene	MP:0003051	curly tail		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0003178	left pulmonary isomerism		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12921739
1551147	Lama5	laminin, alpha 5	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20251023	MGI			PMID:27534441
1551147	Lama5	laminin, alpha 5	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:12051813
1551147	Lama5	laminin, alpha 5	gene	MP:0003675	kidney cyst		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20220428	MGI			PMID:28735299
1551147	Lama5	laminin, alpha 5	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:10625553
1551147	Lama5	laminin, alpha 5	gene	MP:0003813	abnormal hair follicle dermal papilla morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:28735299
1551147	Lama5	laminin, alpha 5	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0004157	interrupted aortic arch		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0004733	abnormal thoracic cavity morphology		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12921739
1551147	Lama5	laminin, alpha 5	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847204
1551147	Lama5	laminin, alpha 5	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10625553
1551147	Lama5	laminin, alpha 5	gene	MP:0005327	abnormal mesangial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10625553
1551147	Lama5	laminin, alpha 5	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20251023	MGI			PMID:27534441
1551147	Lama5	laminin, alpha 5	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0005502	abnormal renal/urinary system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1551147	Lama5	laminin, alpha 5	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1551147	Lama5	laminin, alpha 5	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1551147	Lama5	laminin, alpha 5	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:28735299
1551147	Lama5	laminin, alpha 5	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847204
1551147	Lama5	laminin, alpha 5	gene	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847204
1551147	Lama5	laminin, alpha 5	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0009570	abnormal right lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12051813
1551147	Lama5	laminin, alpha 5	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847204
1551147	Lama5	laminin, alpha 5	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23847204
1551147	Lama5	laminin, alpha 5	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0010460	pulmonary artery hypoplasia		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0010487	abnormal right subclavian artery morphology		IEA		N	RGD:5509061	20150827	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0010811	decreased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0010817	absent type I pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0010821	abnormal visceral pleura morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12051813
1551147	Lama5	laminin, alpha 5	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365040
1551147	Lama5	laminin, alpha 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551147	Lama5	laminin, alpha 5	gene	MP:0011144	thin lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936333
1551147	Lama5	laminin, alpha 5	gene	MP:0011159	abnormal epidermal-dermal junction morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:28735299
1551147	Lama5	laminin, alpha 5	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10625553
1551147	Lama5	laminin, alpha 5	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16790509
1551147	Lama5	laminin, alpha 5	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20150535
1551147	Lama5	laminin, alpha 5	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20251023	MGI			PMID:34774562
1551147	Lama5	laminin, alpha 5	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10625553
1551147	Lama5	laminin, alpha 5	gene	MP:0011521	decreased placental labyrinth size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9852162
1551147	Lama5	laminin, alpha 5	gene	MP:0014084	clubbed small intestinal villi		IAGP		N	RGD:5509061	20220428	MGI			PMID:28735299
1551149	Coro7	coronin 7	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:27143109
1551149	Coro7	coronin 7	gene	MP:0011709	increased fibroblast cell migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:27143109
1551149	Coro7	coronin 7	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27143109
1551149	Coro7	coronin 7	gene	MP:0014699	increased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:27143109
1551149	Coro7	coronin 7	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27143109
1551155	Rtn3	reticulon 3	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0002959	increased urine microalbumin level		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20241024	MGI			PMID:25319692
1551155	Rtn3	reticulon 3	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551155	Rtn3	reticulon 3	gene	MP:0011425	abnormal kidney interstitium morphology		IAGP		N	RGD:5509061	20241024	MGI			PMID:35596061
1551159	Yeats4	YEATS domain containing 4	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551159	Yeats4	YEATS domain containing 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200206	MGI			PMID:31434684
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0000519	hydronephrosis		IEA		N	RGD:5509061	20111116	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300902
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001426	polydipsia		IEA		N	RGD:5509061	20111116	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20160421	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300902
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300902
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300902
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0002703	abnormal renal tubule morphology		IEA		N	RGD:5509061	20111116	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0002988	decreased urine osmolality		IEA		N	RGD:5509061	20111116	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0005633	increased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300902
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20160421	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0010858	pulmonary epithelial necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0010861	increased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300902
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300902
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505443
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524855
1551161	Nedd4l	neural precursor cell expressed, developmentally down-regulated gene 4-like	gene	MP:0014206	decreased intestinal epithelial sodium ion transmembrane transport		IAGP		N	RGD:5509061	20160526	MGI			PMID:18524855
1551162	Dnah6	dynein, axonemal, heavy chain 6	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20201022	MGI			
1551162	Dnah6	dynein, axonemal, heavy chain 6	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1551162	Dnah6	dynein, axonemal, heavy chain 6	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20201022	MGI			
1551163	Tas2r105	taste receptor, type 2, member 105	gene	MP:0004210	abnormal bitter taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15759003
1551164	Slx1b	SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1551164	Slx1b	SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20200310	MGI			PMID:24076219
1551164	Slx1b	SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551164	Slx1b	SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20200310	MGI			PMID:24076219
1551164	Slx1b	SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)	gene	MP:0008221	abnormal hippocampal commissure morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551164	Slx1b	SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:26980188
1551164	Slx1b	SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:24076219
1551164	Slx1b	SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)	gene	MP:0012443	increased corpus callosum size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551164	Slx1b	SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)	gene	MP:0012459	increased dentate gyrus size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20210513	MGI			PMID:31924127
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210513	MGI			PMID:31924127
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210805	MGI			PMID:34026442
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20260402	MGI			
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:30926667
1551166	Cnot6l	CCR4-NOT transcription complex, subunit 6-like	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:30926667
1551167	Fbxo30	F-box protein 30	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1551167	Fbxo30	F-box protein 30	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1551167	Fbxo30	F-box protein 30	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1551167	Fbxo30	F-box protein 30	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1551167	Fbxo30	F-box protein 30	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1551167	Fbxo30	F-box protein 30	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1551167	Fbxo30	F-box protein 30	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20201022	MGI			
1551167	Fbxo30	F-box protein 30	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1551167	Fbxo30	F-box protein 30	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482969
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482969
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20170105	MGI			
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482969
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482969
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17369844
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12482969
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0011187	abnormal parietal endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551168	Tsg101	tumor susceptibility gene 101	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11172041
1551171	Smndc1	survival motor neuron domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250102	MGI			PMID:39150991
1551171	Smndc1	survival motor neuron domain containing 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250102	MGI			PMID:39150991
1551171	Smndc1	survival motor neuron domain containing 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250102	MGI			PMID:39150991
1551174	Ncstn	nicastrin	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1551174	Ncstn	nicastrin	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20160714	MGI			PMID:25194568
1551174	Ncstn	nicastrin	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1551174	Ncstn	nicastrin	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1551174	Ncstn	nicastrin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1551174	Ncstn	nicastrin	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1551174	Ncstn	nicastrin	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1551174	Ncstn	nicastrin	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1551174	Ncstn	nicastrin	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1551174	Ncstn	nicastrin	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12815056
1551174	Ncstn	nicastrin	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1551174	Ncstn	nicastrin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1551174	Ncstn	nicastrin	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0003587	ureter obstruction		IAGP		N	RGD:5509061	20160714	MGI			PMID:25194568
1551174	Ncstn	nicastrin	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1551174	Ncstn	nicastrin	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1551174	Ncstn	nicastrin	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1551174	Ncstn	nicastrin	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1551174	Ncstn	nicastrin	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0009550	increased urinary bladder carcinoma incidence		IAGP		N	RGD:5509061	20160714	MGI			PMID:25194568
1551174	Ncstn	nicastrin	gene	MP:0009846	abnormal neural crest morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1551174	Ncstn	nicastrin	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359070
1551174	Ncstn	nicastrin	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12815056
1551174	Ncstn	nicastrin	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19494151
1551174	Ncstn	nicastrin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716934
1551174	Ncstn	nicastrin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1551174	Ncstn	nicastrin	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16626651
1551174	Ncstn	nicastrin	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1551174	Ncstn	nicastrin	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:19494151
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0001586	abnormal erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20190425	MGI			PMID:24510501
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18796632
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:20190135
1551178	Gimap5	GTPase, IMAP family member 5	gene	MP:0014348	decreased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:20190135
1551179	Des	desmin	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0003057	abnormal epicardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490514
1551179	Des	desmin	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0003211	abnormal aorta elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0003819	increased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0003824	decreased left ventricle developed pressure		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0004058	abnormal ventricle papillary muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0004070	abnormal P wave		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250911	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0004567	decreased myocardial fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20171109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626040
1551179	Des	desmin	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9281443
1551179	Des	desmin	gene	MP:0008543	atrial fibrillation		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490514
1551179	Des	desmin	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490514
1551179	Des	desmin	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490514
1551179	Des	desmin	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490514
1551179	Des	desmin	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18490514
1551179	Des	desmin	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0010520	sinoatrial block		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0010553	prolonged HV interval		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20201217	MGI			PMID:25179606
1551179	Des	desmin	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20160428	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591032
1551179	Des	desmin	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:14715896
1551179	Des	desmin	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:8794866
1551179	Des	desmin	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:11827695
1551179	Des	desmin	gene	MP:0031730	atrial premature beat		IAGP		N	RGD:5509061	20260806	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0031757	second degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0031759	high degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:25394388
1551179	Des	desmin	gene	MP:0031762	third degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:25394388
1551182	Pmpca	peptidase (mitochondrial processing) alpha	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1551182	Pmpca	peptidase (mitochondrial processing) alpha	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20201022	MGI			
1551182	Pmpca	peptidase (mitochondrial processing) alpha	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1551182	Pmpca	peptidase (mitochondrial processing) alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551182	Pmpca	peptidase (mitochondrial processing) alpha	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551183	Kif4	kinesin family member 4	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1551183	Kif4	kinesin family member 4	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0012315	impaired learning		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0015006	decreased fetal length		IAGP		N	RGD:5509061	20260611	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0021019	increased dendritic spine number		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551183	Kif4	kinesin family member 4	gene	MP:0021165	behavioral developmental delay		IAGP		N	RGD:5509061	20240905	MGI			PMID:36482480
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11829492
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11829492
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20260402	MGI			
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20260402	MGI			
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20260402	MGI			
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11829492
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0003280	urinary incontinence		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770692
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0008242	abnormal perivascular macrophage morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0008647	increased circulating interleukin-12b level		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770692
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0009105	penis prolapse		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0009246	pale spleen		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770692
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0010894	pulmonary alveolar edema		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11829492
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0011774	abnormal urinary bladder detrusor smooth muscle morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20210218	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0012230	abnormal sphingolipid level		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770692
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20161027	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0012712	spinal cord degeneration		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0014902	increased circulating CCL2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0014972	decreased spleen enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:23681708
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0020116	increased sphingosine level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0020116	increased sphingosine level		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0020955	increased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0030837	abnormal knee joint morphology		IAGP		N	RGD:5509061	20200409	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0031220	increased circulating CXCL10 level		IAGP		N	RGD:5509061	20210218	MGI			PMID:29908121
1551184	Asah1	N-acylsphingosine amidohydrolase 1	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20260122	MGI			PMID:37231125
1551186	Wdr24	WD repeat domain 24	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1551186	Wdr24	WD repeat domain 24	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20230907	MGI			PMID:36732624
1551186	Wdr24	WD repeat domain 24	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1551186	Wdr24	WD repeat domain 24	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551186	Wdr24	WD repeat domain 24	gene	MP:0013243	abnormal carbohydrate metabolism		IAGP		N	RGD:5509061	20230907	MGI			PMID:36732624
1551186	Wdr24	WD repeat domain 24	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1551186	Wdr24	WD repeat domain 24	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20230907	MGI			PMID:36732624
1551190	Larp6	La ribonucleoprotein 6, translational regulator	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1551190	Larp6	La ribonucleoprotein 6, translational regulator	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20200310	MGI			
1551190	Larp6	La ribonucleoprotein 6, translational regulator	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20200310	MGI			
1551190	Larp6	La ribonucleoprotein 6, translational regulator	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20200310	MGI			
1551190	Larp6	La ribonucleoprotein 6, translational regulator	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15569159
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0000526	small inner medullary pyramid		IAGP		N	RGD:5509061	20200310	MGI			PMID:15569159
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15601467
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20200310	MGI			PMID:15601467
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14691482
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109490
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:19217292
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15601467
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18562627
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19217292
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10067894
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:18562627
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19217292
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17086188
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10067894
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11060028
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19217292
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109490
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:21587207
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:17452521
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002219	decreased lymph node number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10067894
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23297132
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14691482
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002379	abnormal oropharyngeal lymphoid tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12150889
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23297132
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002450	abnormal lymph organ development		IAGP		N	RGD:5509061	20200310	MGI			PMID:14691482
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109490
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20200310	MGI			PMID:10067894
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20200310	MGI			PMID:17452521
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109490
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109490
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0003622	ischuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:15569159
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:19217292
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109490
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19109490
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17452521
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18562627
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210520	MGI			
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20200310	MGI			PMID:11060028
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:17086188
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:17452521
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17452521
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10067894
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0008046	absent NK cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:17086188
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17086188
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17452521
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:19217292
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18562627
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18562627
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0009485	distended ileum		IAGP		N	RGD:5509061	20200310	MGI			PMID:10067894
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:17452521
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:17452521
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:17452521
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15601467
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18562627
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10067894
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0011487	abnormal ureteropelvic junction morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15569159
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0011490	ureteropelvic junction stenosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15569159
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0011503	distended jejunum		IAGP		N	RGD:5509061	20200310	MGI			PMID:10067894
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19217292
1551192	Id2	inhibitor of DNA binding 2	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:19217292
1551193	Atp13a5	ATPase type 13A5	gene	MP:0002635	reduced sensorimotor gating		IEA		N	RGD:5509061	20200310	MGI			
1551193	Atp13a5	ATPase type 13A5	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20200310	MGI			
1551194	Steap3	STEAP family member 3	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1551194	Steap3	STEAP family member 3	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0003066	increased liver copper level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1551194	Steap3	STEAP family member 3	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0006349	decreased circulating copper level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16227996
1551194	Steap3	STEAP family member 3	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551194	Steap3	STEAP family member 3	gene	MP:0008996	abnormal blood osmolality		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0009341	decreased splenocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18617898
1551194	Steap3	STEAP family member 3	gene	MP:0010175	leptocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18955558
1551195	Eif3k	eukaryotic translation initiation factor 3, subunit K	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230119	MGI			
1551195	Eif3k	eukaryotic translation initiation factor 3, subunit K	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20230119	MGI			
1551195	Eif3k	eukaryotic translation initiation factor 3, subunit K	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0000520	absent kidney		IEA		N	RGD:5509061	20200310	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20200310	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220908	MGI			PMID:34381067
1551197	Unk	unkempt family zinc finger	gene	MP:0002947	increased hemangioma incidence		IEA		N	RGD:5509061	20210930	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0003722	absent ureter		IEA		N	RGD:5509061	20200310	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0009532	decreased parotid gland size		IEA		N	RGD:5509061	20200310	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20200310	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0010977	fused right lung lobes		IEA		N	RGD:5509061	20200310	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20200310	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20200310	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20200310	MGI			
1551197	Unk	unkempt family zinc finger	gene	MP:0014114	abnormal cognition		IAGP		N	RGD:5509061	20220908	MGI			PMID:34381067
1551198	Unc13b	unc-13 homolog B	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070347
1551198	Unc13b	unc-13 homolog B	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20181227	MGI			
1551198	Unc13b	unc-13 homolog B	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20181227	MGI			
1551198	Unc13b	unc-13 homolog B	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267576
1551198	Unc13b	unc-13 homolog B	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267576
1551198	Unc13b	unc-13 homolog B	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040848
1551198	Unc13b	unc-13 homolog B	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070347
1551198	Unc13b	unc-13 homolog B	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674279
1551198	Unc13b	unc-13 homolog B	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674279
1551198	Unc13b	unc-13 homolog B	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267576
1551198	Unc13b	unc-13 homolog B	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070347
1551198	Unc13b	unc-13 homolog B	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17267576
1551198	Unc13b	unc-13 homolog B	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040848
1551198	Unc13b	unc-13 homolog B	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22674279
1551198	Unc13b	unc-13 homolog B	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070347
1551198	Unc13b	unc-13 homolog B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070347
1551198	Unc13b	unc-13 homolog B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551198	Unc13b	unc-13 homolog B	gene	MP:0015052	abnormal presynaptic active zone morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:21040848
1551198	Unc13b	unc-13 homolog B	gene	MP:0020359	abnormal ribbon synapse morphology		IAGP		N	RGD:5509061	20260730	MGI			PMID:22674279
1551198	Unc13b	unc-13 homolog B	gene	MP:0021009	abnormal synaptic physiology		IAGP		N	RGD:5509061	20260813	MGI			PMID:17267576
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0000088	short mandible		IEA		N	RGD:5509061	20111116	MGI			
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538759
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210128	MGI			
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17943079
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0003755	abnormal palate morphology		IEA		N	RGD:5509061	20111116	MGI			
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0003756	abnormal hard palate morphology		IEA		N	RGD:5509061	20111215	MGI			
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16179481
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:16341262
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0006369	supernumerary incisors		IEA		N	RGD:5509061	20111116	MGI			
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0008525	decreased cranium height		IEA		N	RGD:5509061	20111116	MGI			
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0008526	decreased cranium width		IEA		N	RGD:5509061	20111116	MGI			
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16341262
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19782673
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16341262
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0010773	supernumerary molars		IAGP		N	RGD:5509061	20171228	MGI			PMID:16179481
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0010864	abnormal enamel knot morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:16179481
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538759
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0011372	decreased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16341262
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:20197625
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20160602	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0030438	increased osteoblast proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:24789067
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:16179481
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0030473	fused molars		IAGP		N	RGD:5509061	20171228	MGI			PMID:16179481
1551201	Sostdc1	sclerostin domain containing 1	gene	MP:0030473	fused molars		IAGP		N	RGD:5509061	20171228	MGI			PMID:16341262
1551202	Noc4l	NOC4 like	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1551202	Noc4l	NOC4 like	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1551202	Noc4l	NOC4 like	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28012024
1551202	Noc4l	NOC4 like	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1551202	Noc4l	NOC4 like	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1551202	Noc4l	NOC4 like	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28012024
1551203	Spam1	sperm adhesion molecule 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20200310	MGI			PMID:12065596
1551203	Spam1	sperm adhesion molecule 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20200310	MGI			PMID:19605784
1551203	Spam1	sperm adhesion molecule 1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19605784
1551204	Degs2	delta 4-desaturase, sphingolipid 2	gene	MP:0020583	decreased ceramide level		IAGP		N	RGD:5509061	20231109	MGI			PMID:36907437
1551206	Olfml2b	olfactomedin-like 2B	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20231207	MGI			
1551210	Pafah2	platelet-activating factor acetylhydrolase 2	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18024956
1551210	Pafah2	platelet-activating factor acetylhydrolase 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18024956
1551210	Pafah2	platelet-activating factor acetylhydrolase 2	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18024956
1551212	Dnajc18	DnaJ heat shock protein family (Hsp40) member C18	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551215	Cdc37l1	cell division cycle 37-like 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1551215	Cdc37l1	cell division cycle 37-like 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
1551215	Cdc37l1	cell division cycle 37-like 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20200310	MGI			
1551215	Cdc37l1	cell division cycle 37-like 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1551220	Lmbr1l	limb region 1 like	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20200310	MGI			
1551220	Lmbr1l	limb region 1 like	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0002491	decreased IgD level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1551220	Lmbr1l	limb region 1 like	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0011181	increased hematopoietic cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0012762	abnormal alpha-beta T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551220	Lmbr1l	limb region 1 like	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:31073040
1551221	Babam2	BRISC and BRCA1 A complex member 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
1551221	Babam2	BRISC and BRCA1 A complex member 2	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20141003	MGI			
1551221	Babam2	BRISC and BRCA1 A complex member 2	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1551221	Babam2	BRISC and BRCA1 A complex member 2	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20170615	MGI			PMID:27001068
1551221	Babam2	BRISC and BRCA1 A complex member 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20170615	MGI			PMID:27001068
1551221	Babam2	BRISC and BRCA1 A complex member 2	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20170615	MGI			PMID:27001068
1551221	Babam2	BRISC and BRCA1 A complex member 2	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:27001068
1551226	Sec23ip	Sec23 interacting protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640725
1551226	Sec23ip	Sec23 interacting protein	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20230309	MGI			PMID:21640725
1551226	Sec23ip	Sec23 interacting protein	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640725
1551226	Sec23ip	Sec23 interacting protein	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:21640725
1551226	Sec23ip	Sec23 interacting protein	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20230309	MGI			PMID:21640725
1551226	Sec23ip	Sec23 interacting protein	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:21640725
1551226	Sec23ip	Sec23 interacting protein	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:21640725
1551226	Sec23ip	Sec23 interacting protein	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20230309	MGI			PMID:21640725
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210520	MGI			
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20220519	MGI			
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20260402	MGI			
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20260402	MGI			
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0006206	embryonic lethality between somite formation and embryo turning		IEA		N	RGD:5509061	20141003	MGI			
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1551227	Cct3	chaperonin containing TCP1 subunit 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1551231	Tmem64	transmembrane protein 64	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551231	Tmem64	transmembrane protein 64	gene	MP:0030984	increased circulating osteocalcin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23395171
1551233	Marchf8	membrane associated ring-CH-type finger 8	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20200514	MGI			
1551233	Marchf8	membrane associated ring-CH-type finger 8	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20200514	MGI			
1551233	Marchf8	membrane associated ring-CH-type finger 8	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20250508	MGI			
1551233	Marchf8	membrane associated ring-CH-type finger 8	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1551233	Marchf8	membrane associated ring-CH-type finger 8	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20240523	MGI			
1551233	Marchf8	membrane associated ring-CH-type finger 8	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551233	Marchf8	membrane associated ring-CH-type finger 8	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20250508	MGI			
1551233	Marchf8	membrane associated ring-CH-type finger 8	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20260402	MGI			
1551235	Bcap29	B cell receptor associated protein 29	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220519	MGI			
1551235	Bcap29	B cell receptor associated protein 29	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1551235	Bcap29	B cell receptor associated protein 29	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22144916
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:22144916
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24721909
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22144916
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001349	excessive tearing		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:22144916
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0002368	abnormal thymus capsule morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0003442	decreased circulating glycerol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004666	absent stapedial artery		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0008805	decreased circulating amylase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:22144916
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0008861	abnormal hair shedding		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0008861	abnormal hair shedding		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0009770	abnormal optic chiasm morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0011655	abnormal systemic artery morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013826	absent hypoglossal canal		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013842	ductus venosus stenosis		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013875	increased trigeminal neuroma incidence		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013928	thin motoric part of trigeminal nerve		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013948	intraembryonal intestine elongation		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013992	persistent dorsal ophthalmic artery		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0013995	abnormal external carotid artery origin		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20200310	MGI			
1551238	Nsun2	NOL1/NOP2/Sun domain family member 2	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20200310	MGI			
1551239	Arfip2	ARF interacting protein 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20260402	MGI			
1551239	Arfip2	ARF interacting protein 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20240328	MGI			PMID:38247505
1551239	Arfip2	ARF interacting protein 2	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20260402	MGI			
1551239	Arfip2	ARF interacting protein 2	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38247505
1551239	Arfip2	ARF interacting protein 2	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38247505
1551239	Arfip2	ARF interacting protein 2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20240328	MGI			PMID:38247505
1551239	Arfip2	ARF interacting protein 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1551239	Arfip2	ARF interacting protein 2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20240328	MGI			PMID:38247505
1551241	St3gal1	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:10755614
1551241	St3gal1	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:12077344
1551242	Tspan3	tetraspanin 3	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20160623	MGI			PMID:26212080
1551242	Tspan3	tetraspanin 3	gene	MP:0011995	decreased leukemia incidence		IAGP		N	RGD:5509061	20160623	MGI			PMID:26212080
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:25557619
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25557619
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25557619
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0020078	decreased brain tyrosine 3-monooxygenase activity		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0020875	decreased nervous system dopamine level		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551245	Gch1	GTP cyclohydrolase 1	gene	MP:0030697	increased phenylalanine level		IAGP		N	RGD:5509061	20201210	MGI			PMID:30742839
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0002899	fatigue		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0011134	decreased lung endothelial cell migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551247	Aggf1	angiogenic factor with G patch and FHA domains 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27522498
1551248	Lrrc38	leucine rich repeat containing 38	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20231207	MGI			
1551248	Lrrc38	leucine rich repeat containing 38	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1551248	Lrrc38	leucine rich repeat containing 38	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1551248	Lrrc38	leucine rich repeat containing 38	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1551249	Vsx2	visual system homeobox 2	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20150611	MGI			PMID:640793
1551249	Vsx2	visual system homeobox 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:13994395
1551249	Vsx2	visual system homeobox 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:13994395
1551249	Vsx2	visual system homeobox 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223342
1551249	Vsx2	visual system homeobox 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13994395
1551249	Vsx2	visual system homeobox 2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223342
1551249	Vsx2	visual system homeobox 2	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13994395
1551249	Vsx2	visual system homeobox 2	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:13994395
1551249	Vsx2	visual system homeobox 2	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1551249	Vsx2	visual system homeobox 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20111116	MGI			
1551249	Vsx2	visual system homeobox 2	gene	MP:0001929	abnormal gametogenesis		IEA		N	RGD:5509061	20111116	MGI			
1551249	Vsx2	visual system homeobox 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0002697	abnormal eye size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16783634
1551249	Vsx2	visual system homeobox 2	gene	MP:0002697	abnormal eye size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18940589
1551249	Vsx2	visual system homeobox 2	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24267650
1551249	Vsx2	visual system homeobox 2	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20150611	MGI			PMID:1181211
1551249	Vsx2	visual system homeobox 2	gene	MP:0004100	abnormal spinal cord interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18940589
1551249	Vsx2	visual system homeobox 2	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13994395
1551249	Vsx2	visual system homeobox 2	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:640793
1551249	Vsx2	visual system homeobox 2	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223342
1551249	Vsx2	visual system homeobox 2	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:640793
1551249	Vsx2	visual system homeobox 2	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15223342
1551249	Vsx2	visual system homeobox 2	gene	MP:0008503	abnormal spinal cord grey matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24267650
1551249	Vsx2	visual system homeobox 2	gene	MP:0009771	absent optic chiasm		IAGP		N	RGD:5509061	20150611	MGI			PMID:13994395
1551249	Vsx2	visual system homeobox 2	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18940589
1551249	Vsx2	visual system homeobox 2	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028343
1551249	Vsx2	visual system homeobox 2	gene	MP:0012534	abnormal optic fissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0012537	abnormal hyaloid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:827941
1551249	Vsx2	visual system homeobox 2	gene	MP:0013447	Harderian gland hypertrophy		IAGP		N	RGD:5509061	20150205	MGI			PMID:13994395
1551249	Vsx2	visual system homeobox 2	gene	MP:0013454	lacrimal gland hypertrophy		IAGP		N	RGD:5509061	20150205	MGI			PMID:13994395
1551249	Vsx2	visual system homeobox 2	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:18940589
1551250	Trpc7	transient receptor potential cation channel, subfamily C, member 7	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21261756
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0001263	weight loss		IEA		N	RGD:5509061	20141003	MGI			
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0001858	intestinal inflammation		IEA		N	RGD:5509061	20141003	MGI			
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0005036	diarrhea		IEA		N	RGD:5509061	20141003	MGI			
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20141003	MGI			
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0010111	abnormal renal calcium reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14679186
1551251	Trpv5	transient receptor potential cation channel, subfamily V, member 5	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23383183
1551253	Cited4	Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1551253	Cited4	Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 4	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20241121	MGI			
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0000263	absent organized vascular network		IAGP		N	RGD:5509061	20171116	MGI			PMID:25328912
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:25328912
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20171116	MGI			PMID:25328912
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20171116	MGI			PMID:25328912
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20171116	MGI			PMID:25328912
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0010502	ventricle myocardium hypoplasia		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20171116	MGI			PMID:25328912
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20171116	MGI			PMID:25328912
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0030992	atrioventricular cushion hypoplasia		IAGP		N	RGD:5509061	20191128	MGI			PMID:25328912
1551256	Creld1	cysteine-rich with EGF-like domains 1	gene	MP:0031128	cardiovascular shunt		IAGP		N	RGD:5509061	20231116	MGI			PMID:33773996
1551257	Nrp2	neuropilin 2	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891274
1551257	Nrp2	neuropilin 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065093
1551257	Nrp2	neuropilin 2	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726444
1551257	Nrp2	neuropilin 2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17942483
1551257	Nrp2	neuropilin 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019322
1551257	Nrp2	neuropilin 2	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10707971
1551257	Nrp2	neuropilin 2	gene	MP:0001064	absent trochlear nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10707971
1551257	Nrp2	neuropilin 2	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10707971
1551257	Nrp2	neuropilin 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17362911
1551257	Nrp2	neuropilin 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891274
1551257	Nrp2	neuropilin 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019322
1551257	Nrp2	neuropilin 2	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065093
1551257	Nrp2	neuropilin 2	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1551257	Nrp2	neuropilin 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019322
1551257	Nrp2	neuropilin 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891274
1551257	Nrp2	neuropilin 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019322
1551257	Nrp2	neuropilin 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17362911
1551257	Nrp2	neuropilin 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12852851
1551257	Nrp2	neuropilin 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15550623
1551257	Nrp2	neuropilin 2	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019322
1551257	Nrp2	neuropilin 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891274
1551257	Nrp2	neuropilin 2	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434520
1551257	Nrp2	neuropilin 2	gene	MP:0004082	abnormal habenula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10707971
1551257	Nrp2	neuropilin 2	gene	MP:0004106	lymphatic vessel hyperplasia		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1551257	Nrp2	neuropilin 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891274
1551257	Nrp2	neuropilin 2	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434520
1551257	Nrp2	neuropilin 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10707971
1551257	Nrp2	neuropilin 2	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12852851
1551257	Nrp2	neuropilin 2	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065093
1551257	Nrp2	neuropilin 2	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10707971
1551257	Nrp2	neuropilin 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0010197	abnormal lymphatic vessel endothelial cell morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1551257	Nrp2	neuropilin 2	gene	MP:0010368	abnormal lymphatic system physiology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1551257	Nrp2	neuropilin 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12852851
1551257	Nrp2	neuropilin 2	gene	MP:0010860	abnormal anterior commissure pars posterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10707971
1551257	Nrp2	neuropilin 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18657176
1551257	Nrp2	neuropilin 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17362911
1551257	Nrp2	neuropilin 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11891274
1551257	Nrp2	neuropilin 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019322
1551257	Nrp2	neuropilin 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20065093
1551257	Nrp2	neuropilin 2	gene	MP:0011678	abnormal vomeronasal sensory neuron physiology		IAGP		N	RGD:5509061	20150319	MGI			PMID:12019322
1551257	Nrp2	neuropilin 2	gene	MP:0011679	abnormal vomeronasal sensory neuron morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:12019322
1551257	Nrp2	neuropilin 2	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12019322
1551257	Nrp2	neuropilin 2	gene	MP:0014746	abnormal hippocampal mossy fiber innervation pattern		IAGP		N	RGD:5509061	20250911	MGI			PMID:10707971
1551257	Nrp2	neuropilin 2	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:18657176
1551259	Zfp687	zinc finger protein 687	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1551261	Morf4l2	mortality factor 4 like 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923606
1551261	Morf4l2	mortality factor 4 like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923606
1551261	Morf4l2	mortality factor 4 like 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923606
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:19059914
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19059914
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:16651614
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10411532
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:19734231
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:19734231
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19059914
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001606	impaired hematopoiesis		IEA		N	RGD:5509061	20200310	MGI			
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:19923276
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19059914
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894167
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20200310	MGI			PMID:18354038
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:19339614
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:21709234
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:24048899
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:8456301
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20211216	MGI			PMID:31964735
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16123129
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8871615
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0003332	liver abscess		IAGP		N	RGD:5509061	20200310	MGI			PMID:21709234
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:19339614
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9164973
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0003884	decreased macrophage cell number		IEA		N	RGD:5509061	20200310	MGI			
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8871615
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:9169506
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10329607
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10411532
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004795	decreased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8871615
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004821	increased susceptibility to experimental autoimmune uveoretinitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15902435
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004824	decreased susceptibility to experimental autoimmune myasthenia gravis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10201893
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19059914
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20200310	MGI			
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:23999498
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:9687534
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:10329607
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8456301
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:9169506
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9169506
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0005672	increased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008054	abnormal uterine NK cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10411532
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19059914
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8456301
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8871615
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:9164973
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8456301
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265950
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200310	MGI			PMID:8163930
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:8871615
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IEA		N	RGD:5509061	20200310	MGI			
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15902435
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:8871615
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:24048899
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20211216	MGI			PMID:31964735
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19734231
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21709234
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008618	decreased circulating interleukin-12 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19734231
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20211216	MGI			PMID:31964735
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:24048899
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15902435
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19734231
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200310	MGI			PMID:8163930
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:16651614
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0009099	abnormal uterine NK cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10411532
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15902435
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0009394	increased uterine NK cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10411532
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:18552211
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:8871615
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:21709234
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:24048899
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20211216	MGI			PMID:31964735
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0010138	arteritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9687534
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0010139	aortitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9687534
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894167
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19734231
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0010280	increased skeletal tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19059914
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0010331	abnormal apolipoprotein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:9169506
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:8456301
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11390995
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0020928	increased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16123129
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0020940	increased susceptibility to Togaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11390995
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0030483	decreased osteocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0030985	decreased circulating osteocalcin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21308779
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:8456301
1551263	Ifngr1	interferon gamma receptor 1	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:9687534
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000831	diencephalon hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000927	small floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20160929	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0004203	abnormal cranial flexure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0004574	broad limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20160929	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0011065	abnormal kidney epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20160929	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0013197	decreased embryonic cilium number		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:20067783
1551267	Intu	inturned planar cell polarity protein	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0013213	abnormal embryonic neuroepithelium primary cilium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:25774014
1551267	Intu	inturned planar cell polarity protein	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:20067783
1551268	Rln3	relaxin 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416195
1551268	Rln3	relaxin 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416196
1551268	Rln3	relaxin 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416196
1551268	Rln3	relaxin 3	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416195
1551268	Rln3	relaxin 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21887138
1551268	Rln3	relaxin 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416195
1551268	Rln3	relaxin 3	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21887138
1551268	Rln3	relaxin 3	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20161201	MGI			
1551268	Rln3	relaxin 3	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416195
1551268	Rln3	relaxin 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416196
1551268	Rln3	relaxin 3	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1551268	Rln3	relaxin 3	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1551268	Rln3	relaxin 3	gene	MP:0004807	abnormal paired-pulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:21887138
1551268	Rln3	relaxin 3	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416196
1551268	Rln3	relaxin 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416196
1551268	Rln3	relaxin 3	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416196
1551268	Rln3	relaxin 3	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1551268	Rln3	relaxin 3	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416196
1551268	Rln3	relaxin 3	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416196
1551268	Rln3	relaxin 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1551268	Rln3	relaxin 3	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19416196
1551268	Rln3	relaxin 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20230119	MGI			
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20230119	MGI			
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0004831	long incisors		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0009908	protruding tongue		IEA		N	RGD:5509061	20230119	MGI			
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551270	Strada	STE20-related kinase adaptor alpha	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20210923	MGI			PMID:32457579
1551273	Sesn3	sestrin 3	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20160804	MGI			
1551273	Sesn3	sestrin 3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958918
1551273	Sesn3	sestrin 3	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22958918
1551273	Sesn3	sestrin 3	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160804	MGI			
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20200310	MGI			
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0001492	abnormal pilomotor reflex		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23472195
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23097495
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551274	Mboat7	membrane bound O-acyltransferase domain containing 7	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1551275	Dcps	decapping enzyme, scavenger	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1551275	Dcps	decapping enzyme, scavenger	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551275	Dcps	decapping enzyme, scavenger	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551280	H2-T24	histocompatibility 2, T region locus 24	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1551280	H2-T24	histocompatibility 2, T region locus 24	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1551280	H2-T24	histocompatibility 2, T region locus 24	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1551281	Myo9a	myosin IXa	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1551281	Myo9a	myosin IXa	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1551281	Myo9a	myosin IXa	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1551281	Myo9a	myosin IXa	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1551281	Myo9a	myosin IXa	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0003584	bifid ureter		IEA		N	RGD:5509061	20170504	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20170504	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1551281	Myo9a	myosin IXa	gene	MP:0006093	arteriovenous malformation		IEA		N	RGD:5509061	20170504	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1551281	Myo9a	myosin IXa	gene	MP:0009689	abnormal neural tube ventricular layer morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1551281	Myo9a	myosin IXa	gene	MP:0011293	dilated nephron		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0011864	abnormal podocyte adhesion		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0011867	decreased podocyte motility		IAGP		N	RGD:5509061	20210422	MGI			PMID:33412162
1551281	Myo9a	myosin IXa	gene	MP:0013228	brain ventricle stenosis		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1551281	Myo9a	myosin IXa	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1551281	Myo9a	myosin IXa	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551283	Rarres1	retinoic acid receptor responder (tazarotene induced) 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:35541897
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210422	MGI			
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20231207	MGI			
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360959
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20160804	MGI			PMID:25614626
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360959
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360959
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20210422	MGI			
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12149515
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160804	MGI			PMID:25614626
1551284	Gopc	golgi associated PDZ and coiled-coil motif containing	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210422	MGI			
1551286	Ccser2	coiled-coil serine rich 2	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:36795749
1551286	Ccser2	coiled-coil serine rich 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20230601	MGI			PMID:36795749
1551286	Ccser2	coiled-coil serine rich 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230601	MGI			PMID:36795749
1551289	Ppm1h	protein phosphatase 1H (PP2C domain containing)	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20211125	MGI			PMID:34658337
1551298	Ppic	peptidylprolyl isomerase C	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20220317	MGI			PMID:33864384
1551298	Ppic	peptidylprolyl isomerase C	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20220317	MGI			PMID:33864384
1551298	Ppic	peptidylprolyl isomerase C	gene	MP:0009925	increased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20220317	MGI			PMID:33864384
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20221215	MGI			
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20221215	MGI			
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551300	Timm8a1	translocase of inner mitochondrial membrane 8A1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20250424	MGI			PMID:32820032
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808965
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808965
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808965
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808965
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808965
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855380
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20230810	MGI			PMID:33098766
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19070574
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133609
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002492	decreased IgE level		IEA		N	RGD:5509061	20181011	MGI			
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007474
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20230810	MGI			PMID:33098766
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19070574
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587764
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19070574
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:18455451
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:18838546
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196992
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22962683
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20210513	MGI			PMID:33526923
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007474
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810694
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18455451
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18838546
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196992
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368578
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20230810	MGI			PMID:33098766
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808965
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008094	absent memory B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008100	absent plasma cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008174	decreased follicular B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117047
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007474
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11007474
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20230810	MGI			PMID:33098766
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20230810	MGI			PMID:33098766
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:18455451
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808965
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808965
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19808965
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21258321
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0013684	increased early germinal center B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551301	Aicda	activation-induced cytidine deaminase	gene	MP:0013685	decreased late germinal center B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551303	Rnf41	ring finger protein 41	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1551303	Rnf41	ring finger protein 41	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1551303	Rnf41	ring finger protein 41	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20220519	MGI			
1551304	Tmem63a	transmembrane protein 63a	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20201231	MGI			
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20240905	MGI			PMID:38630655
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20240905	MGI			PMID:38630655
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20240905	MGI			PMID:38630655
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20240905	MGI			PMID:38630655
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20240905	MGI			PMID:38630655
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20240905	MGI			PMID:38630655
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0012174	flat head		IAGP		N	RGD:5509061	20240905	MGI			PMID:38630655
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1551306	Cfdp1	craniofacial development protein 1	gene	MP:0014241	abnormal intracellular organelle physiology		IAGP		N	RGD:5509061	20240905	MGI			PMID:38630655
1551307	Zbtb7a	zinc finger and BTB domain containing 7a	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17495164
1551307	Zbtb7a	zinc finger and BTB domain containing 7a	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17495164
1551307	Zbtb7a	zinc finger and BTB domain containing 7a	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17495164
1551307	Zbtb7a	zinc finger and BTB domain containing 7a	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17495164
1551307	Zbtb7a	zinc finger and BTB domain containing 7a	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17495164
1551307	Zbtb7a	zinc finger and BTB domain containing 7a	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17495164
1551307	Zbtb7a	zinc finger and BTB domain containing 7a	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20200310	MGI			PMID:17495164
1551307	Zbtb7a	zinc finger and BTB domain containing 7a	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17495164
1551307	Zbtb7a	zinc finger and BTB domain containing 7a	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17495164
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210826	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20241121	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20241121	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210826	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1551308	Gapvd1	GTPase activating protein and VPS9 domains 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1551310	Commd3	COMM domain containing 3	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20260402	MGI			
1551310	Commd3	COMM domain containing 3	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551310	Commd3	COMM domain containing 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1551310	Commd3	COMM domain containing 3	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551310	Commd3	COMM domain containing 3	gene	MP:0008191	abnormal follicular B cell physiology		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551310	Commd3	COMM domain containing 3	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551310	Commd3	COMM domain containing 3	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551310	Commd3	COMM domain containing 3	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551310	Commd3	COMM domain containing 3	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551310	Commd3	COMM domain containing 3	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551310	Commd3	COMM domain containing 3	gene	MP:0008897	decreased IgG2c level		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551310	Commd3	COMM domain containing 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1551310	Commd3	COMM domain containing 3	gene	MP:0013940	abnormal plasmablast number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31088898
1551312	Aldh3b1	aldehyde dehydrogenase 3 family, member B1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160421	MGI			
1551312	Aldh3b1	aldehyde dehydrogenase 3 family, member B1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1551312	Aldh3b1	aldehyde dehydrogenase 3 family, member B1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765677
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8171324
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8202532
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8171324
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8202532
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765677
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483299
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159518
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8202532
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001928	abnormal ovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:8202532
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483299
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002224	abnormal spleen size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11119498
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8171324
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8202532
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8202532
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765677
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0003211	abnormal aorta elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890699
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483299
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0003356	impaired luteinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0003579	increased ovarian carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159518
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19196868
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159518
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11119498
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005040	abnormal MHC II cell surface expression on macrophages		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483299
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483299
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8202532
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483299
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159518
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262803
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141211	MGI			PMID:24633240
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765677
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8171324
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8202532
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0008903	abnormal mesenteric fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765677
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0009020	prolonged metestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10684813
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0010998	pulmonary alveolar proteinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0010998	pulmonary alveolar proteinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8202532
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732663
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0011640	abnormal aorta collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890699
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0012098	increased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0012109	decreased trophoblast glycogen cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9915988
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170202	MGI			PMID:16276414
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20180726	MGI			PMID:8018921
1551314	Csf2	colony stimulating factor 2 (granulocyte-macrophage)	gene	MP:0030974	enhanced gluconeogenesis		IAGP		N	RGD:5509061	20200102	MGI			PMID:18765677
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0002893	ketoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0012172	abnormal amniotic fluid composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0012677	absent brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551315	Slc25a19	solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035501
1551318	Dnajc7	DnaJ heat shock protein family (Hsp40) member C7	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1551318	Dnajc7	DnaJ heat shock protein family (Hsp40) member C7	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1551318	Dnajc7	DnaJ heat shock protein family (Hsp40) member C7	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160407	MGI			PMID:25542016
1551318	Dnajc7	DnaJ heat shock protein family (Hsp40) member C7	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20160407	MGI			PMID:25542016
1551318	Dnajc7	DnaJ heat shock protein family (Hsp40) member C7	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1551319	Angel2	angel homolog 2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20230223	MGI			PMID:36180430
1551319	Angel2	angel homolog 2	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20230223	MGI			PMID:36180430
1551319	Angel2	angel homolog 2	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20230223	MGI			PMID:36180430
1551319	Angel2	angel homolog 2	gene	MP:0014906	abnormal muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:36180430
1551319	Angel2	angel homolog 2	gene	MP:0031746	abnormal mitochondrial translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:36180430
1551322	Klk4	kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551322	Klk4	kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578120
1551322	Klk4	kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578120
1551322	Klk4	kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578120
1551322	Klk4	kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551322	Klk4	kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20151210	MGI			PMID:24360809
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366192
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000467	abnormal esophagus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001241	absent epidermis stratum corneum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002649	abnormal enamel rod pattern		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0003160	abnormal esophagus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366192
1551327	Irf6	interferon regulatory factor 6	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20151210	MGI			PMID:24360809
1551327	Irf6	interferon regulatory factor 6	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21918538
1551327	Irf6	interferon regulatory factor 6	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0004537	abnormal palatine bone horizontal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20171019	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1551327	Irf6	interferon regulatory factor 6	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22366192
1551327	Irf6	interferon regulatory factor 6	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210520	MGI			
1551327	Irf6	interferon regulatory factor 6	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009441	delayed skin barrier formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009474	thick epidermis stratum spinosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20151210	MGI			PMID:24360809
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009884	palatal shelf fusion with tongue or mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009884	palatal shelf fusion with tongue or mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1551327	Irf6	interferon regulatory factor 6	gene	MP:0010096	abnormal incisor color		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151210	MGI			PMID:24360809
1551327	Irf6	interferon regulatory factor 6	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17041603
1551327	Irf6	interferon regulatory factor 6	gene	MP:0011089	perinatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1551327	Irf6	interferon regulatory factor 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151210	MGI			PMID:24360809
1551327	Irf6	interferon regulatory factor 6	gene	MP:0013531	abnormal periderm development		IAGP		N	RGD:5509061	20151210	MGI			PMID:24360809
1551327	Irf6	interferon regulatory factor 6	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:24360809
1551327	Irf6	interferon regulatory factor 6	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0030188	round snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17041601
1551327	Irf6	interferon regulatory factor 6	gene	MP:0030328	glossopalatal ankylosis		IAGP		N	RGD:5509061	20221103	MGI			PMID:20196077
1551327	Irf6	interferon regulatory factor 6	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0030494	abnormal molar root morphology		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0030496	taurodontia		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0030525	abnormal Hertwig epithelial root sheath morphology		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551327	Irf6	interferon regulatory factor 6	gene	MP:0030544	abnormal enamel development		IAGP		N	RGD:5509061	20190711	MGI			PMID:27369589
1551328	Zfp142	zinc finger protein 142	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20260409	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20260409	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20260409	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20260507	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20260409	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0003460	decreased fear-related response		IAGP		N	RGD:5509061	20260409	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20260507	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20260409	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20260409	MGI			PMID:38296634
1551328	Zfp142	zinc finger protein 142	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20260409	MGI			PMID:38296634
1551333	Hpcal1	hippocalcin-like 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20221222	MGI			PMID:36438486
1551333	Hpcal1	hippocalcin-like 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20221222	MGI			PMID:36438486
1551333	Hpcal1	hippocalcin-like 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20221222	MGI			PMID:36438486
1551333	Hpcal1	hippocalcin-like 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20221222	MGI			PMID:36438486
1551333	Hpcal1	hippocalcin-like 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20221222	MGI			PMID:36438486
1551333	Hpcal1	hippocalcin-like 1	gene	MP:0030673	increased circulating alanine level		IAGP		N	RGD:5509061	20221222	MGI			PMID:36438486
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0005520	impaired pancreas regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16083722
1551337	Spink1	serine peptidase inhibitor, Kazal type 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18386042
1551338	Ift88	intraflagellar transport 88	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228099
1551338	Ift88	intraflagellar transport 88	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1551338	Ift88	intraflagellar transport 88	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20240125	MGI			PMID:30289203
1551338	Ift88	intraflagellar transport 88	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1551338	Ift88	intraflagellar transport 88	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1551338	Ift88	intraflagellar transport 88	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1551338	Ift88	intraflagellar transport 88	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1551338	Ift88	intraflagellar transport 88	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1551338	Ift88	intraflagellar transport 88	gene	MP:0000898	midbrain hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228099
1551338	Ift88	intraflagellar transport 88	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1551338	Ift88	intraflagellar transport 88	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1551338	Ift88	intraflagellar transport 88	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228099
1551338	Ift88	intraflagellar transport 88	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200310	MGI			
1551338	Ift88	intraflagellar transport 88	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20200310	MGI			
1551338	Ift88	intraflagellar transport 88	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1551338	Ift88	intraflagellar transport 88	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1551338	Ift88	intraflagellar transport 88	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20210805	MGI			PMID:34186026
1551338	Ift88	intraflagellar transport 88	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228099
1551338	Ift88	intraflagellar transport 88	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15226261
1551338	Ift88	intraflagellar transport 88	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20200310	MGI			PMID:17359961
1551338	Ift88	intraflagellar transport 88	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20240125	MGI			PMID:30289203
1551338	Ift88	intraflagellar transport 88	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15580285
1551338	Ift88	intraflagellar transport 88	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15226261
1551338	Ift88	intraflagellar transport 88	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15580285
1551338	Ift88	intraflagellar transport 88	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8952527
1551338	Ift88	intraflagellar transport 88	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17359961
1551338	Ift88	intraflagellar transport 88	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8952527
1551338	Ift88	intraflagellar transport 88	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:15226261
1551338	Ift88	intraflagellar transport 88	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:15580285
1551338	Ift88	intraflagellar transport 88	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0003462	abnormal response to novel odor		IAGP		N	RGD:5509061	20210805	MGI			PMID:34186026
1551338	Ift88	intraflagellar transport 88	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0003840	abnormal coronal suture morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1551338	Ift88	intraflagellar transport 88	gene	MP:0004203	abnormal cranial flexure morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1551338	Ift88	intraflagellar transport 88	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20200310	MGI			PMID:15226261
1551338	Ift88	intraflagellar transport 88	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20200310	MGI			PMID:15580285
1551338	Ift88	intraflagellar transport 88	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0004574	broad limb buds		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0004574	broad limb buds		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228099
1551338	Ift88	intraflagellar transport 88	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15580285
1551338	Ift88	intraflagellar transport 88	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1551338	Ift88	intraflagellar transport 88	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15580285
1551338	Ift88	intraflagellar transport 88	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228099
1551338	Ift88	intraflagellar transport 88	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:17166921
1551338	Ift88	intraflagellar transport 88	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8952527
1551338	Ift88	intraflagellar transport 88	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0009143	abnormal pancreatic duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0009143	abnormal pancreatic duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0009143	abnormal pancreatic duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15226261
1551338	Ift88	intraflagellar transport 88	gene	MP:0009145	abnormal pancreatic acinus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15580285
1551338	Ift88	intraflagellar transport 88	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15226261
1551338	Ift88	intraflagellar transport 88	gene	MP:0009149	decreased pancreatic acinar cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0009150	pancreatic acinar cell atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31226309
1551338	Ift88	intraflagellar transport 88	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1551338	Ift88	intraflagellar transport 88	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0010041	absent oval cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:11773599
1551338	Ift88	intraflagellar transport 88	gene	MP:0010042	abnormal oval cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20240125	MGI			PMID:30289203
1551338	Ift88	intraflagellar transport 88	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20240125	MGI			PMID:30289203
1551338	Ift88	intraflagellar transport 88	gene	MP:0010436	abnormal coronary sinus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0010440	anomalous pulmonary venous connection		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0010440	anomalous pulmonary venous connection		IAGP		N	RGD:5509061	20240125	MGI			PMID:30289203
1551338	Ift88	intraflagellar transport 88	gene	MP:0010521	absent pulmonary artery		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0010548	abnormal dorsal mesocardium morphology		IAGP		N	RGD:5509061	20240125	MGI			PMID:30289203
1551338	Ift88	intraflagellar transport 88	gene	MP:0010614	abnormal mitral valve cusp morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1551338	Ift88	intraflagellar transport 88	gene	MP:0010773	supernumerary molars		IAGP		N	RGD:5509061	20200310	MGI			PMID:12701101
1551338	Ift88	intraflagellar transport 88	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11062270
1551338	Ift88	intraflagellar transport 88	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:8191288
1551338	Ift88	intraflagellar transport 88	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:8952527
1551338	Ift88	intraflagellar transport 88	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10804177
1551338	Ift88	intraflagellar transport 88	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1551338	Ift88	intraflagellar transport 88	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1551338	Ift88	intraflagellar transport 88	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228099
1551338	Ift88	intraflagellar transport 88	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551338	Ift88	intraflagellar transport 88	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19036983
1551338	Ift88	intraflagellar transport 88	gene	MP:0012531	delayed limb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22228099
1551338	Ift88	intraflagellar transport 88	gene	MP:0013206	abnormal motile cilium morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1551338	Ift88	intraflagellar transport 88	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1551338	Ift88	intraflagellar transport 88	gene	MP:0014093	decreased pancreatic primary cilium length		IAGP		N	RGD:5509061	20200310	MGI			PMID:15226261
1551338	Ift88	intraflagellar transport 88	gene	MP:0014093	decreased pancreatic primary cilium length		IAGP		N	RGD:5509061	20200310	MGI			PMID:15580285
1551338	Ift88	intraflagellar transport 88	gene	MP:0014094	decreased pancreatic primary cilium number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15226261
1551338	Ift88	intraflagellar transport 88	gene	MP:0014094	decreased pancreatic primary cilium number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15580285
1551340	Dnajc28	DnaJ heat shock protein family (Hsp40) member C28	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1551340	Dnajc28	DnaJ heat shock protein family (Hsp40) member C28	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20160421	MGI			
1551341	Cd209c	CD209c antigen	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1551341	Cd209c	CD209c antigen	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1551341	Cd209c	CD209c antigen	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20240523	MGI			
1551344	Gucy2g	guanylate cyclase 2g	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18199799
1551347	Myo1f	myosin IF	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17023661
1551347	Myo1f	myosin IF	gene	MP:0014695	increased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:17023661
1551348	Man1a2	mannosidase, alpha, class 1A, member 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17121831
1551348	Man1a2	mannosidase, alpha, class 1A, member 2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17121831
1551348	Man1a2	mannosidase, alpha, class 1A, member 2	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:17121831
1551348	Man1a2	mannosidase, alpha, class 1A, member 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17121831
1551348	Man1a2	mannosidase, alpha, class 1A, member 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:17121831
1551348	Man1a2	mannosidase, alpha, class 1A, member 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17121831
1551348	Man1a2	mannosidase, alpha, class 1A, member 2	gene	MP:0010909	pulmonary alveolar hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:17121831
1551348	Man1a2	mannosidase, alpha, class 1A, member 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17121831
1551349	Nek2	NIMA (never in mitosis gene a)-related expressed kinase 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1551349	Nek2	NIMA (never in mitosis gene a)-related expressed kinase 2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20181227	MGI			
1551349	Nek2	NIMA (never in mitosis gene a)-related expressed kinase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1551349	Nek2	NIMA (never in mitosis gene a)-related expressed kinase 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1551349	Nek2	NIMA (never in mitosis gene a)-related expressed kinase 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1551349	Nek2	NIMA (never in mitosis gene a)-related expressed kinase 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1551350	Ganab	alpha glucosidase 2 alpha neutral subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210506	MGI			PMID:32550232
1551350	Ganab	alpha glucosidase 2 alpha neutral subunit	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20210506	MGI			PMID:32550232
1551351	St3gal2	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:12393657
1551351	St3gal2	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23118208
1551351	St3gal2	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23118208
1551351	St3gal2	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20200310	MGI			PMID:23118208
1551351	St3gal2	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23118208
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210128	MGI			
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172387
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172387
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20170713	MGI			PMID:28570559
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172387
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172387
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12663541
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172387
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16222339
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:16890500
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16172387
1551353	Polq	polymerase (DNA directed), theta	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1551356	Thtpa	thiamine triphosphatase	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20250508	MGI			
1551356	Thtpa	thiamine triphosphatase	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1551356	Thtpa	thiamine triphosphatase	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1551356	Thtpa	thiamine triphosphatase	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000296	absent trabeculae carneae		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203811
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12824469
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12954715
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12824469
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18760695
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12824469
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001072	abnormal vestibulocochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203811
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378872
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12145742
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203811
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12954715
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203811
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023653
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378872
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0002271	abnormal pulmonary alveolar duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203811
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203811
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378872
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:12145742
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0004567	decreased myocardial fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0004780	abnormal surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203811
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203811
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203811
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12824469
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12954715
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378872
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378872
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22378872
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12824469
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18760695
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12824469
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477376
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12824469
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20150611	MGI			PMID:12824469
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0014721	increased polyploid cardiomyocyte number		IAGP		N	RGD:5509061	20250911	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0015069	increased myocardial fiber length		IAGP		N	RGD:5509061	20260813	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22378872
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15863464
1551357	Erbb4	erb-b2 receptor tyrosine kinase 4	gene	MP:0031717	prolonged corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:15863464
1551360	Prkcq	protein kinase C, theta	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15592506
1551360	Prkcq	protein kinase C, theta	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084656
1551360	Prkcq	protein kinase C, theta	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20170105	MGI			
1551360	Prkcq	protein kinase C, theta	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20170105	MGI			
1551360	Prkcq	protein kinase C, theta	gene	MP:0001267	enlarged chest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15592506
1551360	Prkcq	protein kinase C, theta	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20170720	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:15592506
1551360	Prkcq	protein kinase C, theta	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20180215	MGI			
1551360	Prkcq	protein kinase C, theta	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746729
1551360	Prkcq	protein kinase C, theta	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1551360	Prkcq	protein kinase C, theta	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372106
1551360	Prkcq	protein kinase C, theta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15592506
1551360	Prkcq	protein kinase C, theta	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155788
1551360	Prkcq	protein kinase C, theta	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782715
1551360	Prkcq	protein kinase C, theta	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372106
1551360	Prkcq	protein kinase C, theta	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084656
1551360	Prkcq	protein kinase C, theta	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20170202	MGI			PMID:27603725
1551360	Prkcq	protein kinase C, theta	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:27603725
1551360	Prkcq	protein kinase C, theta	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15084656
1551360	Prkcq	protein kinase C, theta	gene	MP:0004130	abnormal muscle cell glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372106
1551360	Prkcq	protein kinase C, theta	gene	MP:0004185	abnormal adipocyte glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372106
1551360	Prkcq	protein kinase C, theta	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493044
1551360	Prkcq	protein kinase C, theta	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155788
1551360	Prkcq	protein kinase C, theta	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15592506
1551360	Prkcq	protein kinase C, theta	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182568
1551360	Prkcq	protein kinase C, theta	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
1551360	Prkcq	protein kinase C, theta	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155788
1551360	Prkcq	protein kinase C, theta	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155788
1551360	Prkcq	protein kinase C, theta	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746729
1551360	Prkcq	protein kinase C, theta	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782715
1551360	Prkcq	protein kinase C, theta	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
1551360	Prkcq	protein kinase C, theta	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182568
1551360	Prkcq	protein kinase C, theta	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155708
1551360	Prkcq	protein kinase C, theta	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155788
1551360	Prkcq	protein kinase C, theta	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20170720	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18815612
1551360	Prkcq	protein kinase C, theta	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0006237	abnormal choroid vasculature morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:27603725
1551360	Prkcq	protein kinase C, theta	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18815612
1551360	Prkcq	protein kinase C, theta	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18842300
1551360	Prkcq	protein kinase C, theta	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182568
1551360	Prkcq	protein kinase C, theta	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18842300
1551360	Prkcq	protein kinase C, theta	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155788
1551360	Prkcq	protein kinase C, theta	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155788
1551360	Prkcq	protein kinase C, theta	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:27603725
1551360	Prkcq	protein kinase C, theta	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493044
1551360	Prkcq	protein kinase C, theta	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493044
1551360	Prkcq	protein kinase C, theta	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10746729
1551360	Prkcq	protein kinase C, theta	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782715
1551360	Prkcq	protein kinase C, theta	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493044
1551360	Prkcq	protein kinase C, theta	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493044
1551360	Prkcq	protein kinase C, theta	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18155708
1551360	Prkcq	protein kinase C, theta	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0008747	abnormal T cell anergy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
1551360	Prkcq	protein kinase C, theta	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528385
1551360	Prkcq	protein kinase C, theta	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024044
1551360	Prkcq	protein kinase C, theta	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16493044
1551360	Prkcq	protein kinase C, theta	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18815612
1551360	Prkcq	protein kinase C, theta	gene	MP:0009586	increased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18815612
1551360	Prkcq	protein kinase C, theta	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:26978024
1551360	Prkcq	protein kinase C, theta	gene	MP:0010130	decreased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155788
1551360	Prkcq	protein kinase C, theta	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155788
1551360	Prkcq	protein kinase C, theta	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15592506
1551360	Prkcq	protein kinase C, theta	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20180215	MGI			
1551360	Prkcq	protein kinase C, theta	gene	MP:0020442	serous retina detachment		IAGP		N	RGD:5509061	20170907	MGI			PMID:26978024
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601035
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905411
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590934
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601035
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601035
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905411
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601035
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905411
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601035
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0002653	abnormal ependyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590934
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590934
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20211021	MGI			
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905411
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590934
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590934
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590934
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004450	presphenoid bone hypoplasia		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004475	palatine bone hypoplasia		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601035
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905411
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0009771	absent optic chiasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0009900	vomer bone hypoplasia		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15590934
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601035
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15905411
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0011266	abnormal frontonasal mesenchyme morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20231221	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0014276	lobar holoprosencephaly		IAGP		N	RGD:5509061	20230810	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0014750	abnormal retinal ganglion cell axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:10601035
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0030137	abnormal upper incisor morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0030274	maxillary retrognathia		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0030476	fused upper incisors		IAGP		N	RGD:5509061	20171228	MGI			PMID:10601036
1551361	Vax1	ventral anterior homeobox 1	gene	MP:0031457	abnormal vomeronasal cartilage morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:28771384
1551364	Zfp160	zinc finger protein 160	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1551364	Zfp160	zinc finger protein 160	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1551364	Zfp160	zinc finger protein 160	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20220519	MGI			
1551364	Zfp160	zinc finger protein 160	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1551364	Zfp160	zinc finger protein 160	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1551365	Ctnnd2	catenin delta 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380068
1551365	Ctnnd2	catenin delta 2	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380068
1551365	Ctnnd2	catenin delta 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380068
1551365	Ctnnd2	catenin delta 2	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380068
1551365	Ctnnd2	catenin delta 2	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380068
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20200402	MGI			
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0008168	decreased B-1a cell number		IEA		N	RGD:5509061	20201231	MGI			
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0008174	decreased follicular B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0008211	decreased mature B cell number		IEA		N	RGD:5509061	20170105	MGI			
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0009922	increased transitional stage T1 B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20200402	MGI			
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0013797	abnormal ileal goblet cell morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551368	Arhgap17	Rho GTPase activating protein 17	gene	MP:0014201	abnormal intestinal epithelium physiology		IAGP		N	RGD:5509061	20191107	MGI			PMID:27229483
1551369	Gtpbp6	GTP binding protein 6 (putative)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230601	MGI			
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0005314	absent thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0010017	visceral vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870284
1551371	Abca5	ATP-binding cassette, sub-family A member 5	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:15870284
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200514	MGI			
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1551372	Fgf12	fibroblast growth factor 12	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1551373	Fibp	fibroblast growth factor (acidic) intracellular binding protein	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20221110	MGI			
1551373	Fibp	fibroblast growth factor (acidic) intracellular binding protein	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221110	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:29920190
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0002691	small stomach		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0003641	small lung		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20211021	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29920190
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29920190
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29920190
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29920190
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:29920190
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1551375	Hectd3	HECT domain E3 ubiquitin protein ligase 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200310	MGI			
1551376	Alpk3	alpha-kinase 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0010545	abnormal heart layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20210128	MGI			
1551376	Alpk3	alpha-kinase 3	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0010754	abnormal heart left ventricle pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551376	Alpk3	alpha-kinase 3	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0014731	disorganized myocardial fiber myofibrils		IAGP		N	RGD:5509061	20250911	MGI			PMID:21441111
1551376	Alpk3	alpha-kinase 3	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:21441111
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20220519	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1551377	Erlin1	ER lipid raft associated 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1551379	Rap1gap	Rap1 GTPase-activating protein	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551379	Rap1gap	Rap1 GTPase-activating protein	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1551379	Rap1gap	Rap1 GTPase-activating protein	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551379	Rap1gap	Rap1 GTPase-activating protein	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1551379	Rap1gap	Rap1 GTPase-activating protein	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1551379	Rap1gap	Rap1 GTPase-activating protein	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1551380	Sypl2	synaptophysin like 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:10613905
1551380	Sypl2	synaptophysin like 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10613905
1551380	Sypl2	synaptophysin like 2	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:10613905
1551380	Sypl2	synaptophysin like 2	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10613905
1551380	Sypl2	synaptophysin like 2	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10613905
1551380	Sypl2	synaptophysin like 2	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10613905
1551380	Sypl2	synaptophysin like 2	gene	MP:0009411	abnormal skeletal muscle fiber triad morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10613905
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21138943
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21138943
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21138943
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21138943
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0005604	hyperekplexia		IEA		N	RGD:5509061	20111116	MGI			
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20150917	MGI			PMID:23540940
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20150917	MGI			PMID:23540940
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0010570	prolonged ST segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0010636	bundle branch block		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965931
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150917	MGI			PMID:23540940
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0011303	absent kidney papilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:21138943
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20150917	MGI			PMID:23540940
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:17618853
1551381	Esrrg	estrogen-related receptor gamma	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:23540940
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20160804	MGI			
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20170824	MGI			PMID:28248300
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0009611	epidermis stratum spinosum hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0010535	myocardium steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0011579	decreased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20023287
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0011582	decreased triglyceride lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20170824	MGI			PMID:28248300
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0030018	increased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:23733885
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0031418	increased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23413028
1551382	Abhd5	abhydrolase domain containing 5	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:23413028
1551383	Ifi47	interferon gamma inducible protein 47	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11457893
1551388	Mtrex	Mtr4 exosome RNA helicase	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:39378876
1551388	Mtrex	Mtr4 exosome RNA helicase	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20250508	MGI			PMID:39378876
1551388	Mtrex	Mtr4 exosome RNA helicase	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20250508	MGI			PMID:39378876
1551388	Mtrex	Mtr4 exosome RNA helicase	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20250508	MGI			PMID:39378876
1551388	Mtrex	Mtr4 exosome RNA helicase	gene	MP:0008887	abnormal splicing factor domain morphology		IAGP		N	RGD:5509061	20250508	MGI			PMID:39378876
1551388	Mtrex	Mtr4 exosome RNA helicase	gene	MP:0009375	thin zona pellucida		IAGP		N	RGD:5509061	20250508	MGI			PMID:39378876
1551390	Usp36	ubiquitin specific peptidase 36	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:29273634
1551390	Usp36	ubiquitin specific peptidase 36	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20200310	MGI			
1551390	Usp36	ubiquitin specific peptidase 36	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29273634
1551390	Usp36	ubiquitin specific peptidase 36	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29273634
1551390	Usp36	ubiquitin specific peptidase 36	gene	MP:0012129	failure of blastocyst formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:29273634
1551390	Usp36	ubiquitin specific peptidase 36	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29273634
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:6893636|PMID:18551038	20120913	RGD			
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:6893636|PMID:18551038	20120913	RGD			
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20638879
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:19204075
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:20638879
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:11181567
1551392	Mthfr	methylenetetrahydrofolate reductase	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:11181567
1551394	Pon2	paraoxonase 2	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1551394	Pon2	paraoxonase 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551394	Pon2	paraoxonase 2	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16891303
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20200310	MGI			PMID:16715502
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:22418434
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20200310	MGI			PMID:16715502
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22418434
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22418434
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22418434
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16715502
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0012535	abnormal optic fissure closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689267
1551398	Nuak1	NUAK family, SNF1-like kinase, 1	gene	MP:0031617	abnormal skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:22418434
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24006281
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24006281
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20200310	MGI			
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0002546	mydriasis		IEA		N	RGD:5509061	20200310	MGI			
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24006281
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20200310	MGI			
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24006281
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24006281
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:24006281
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24006281
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:24006281
1551400	Jmjd1c	jumonji domain containing 1C	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:24006281
1551401	Sec11c	SEC11 homolog C, signal peptidase complex subunit	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20160421	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20170105	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20201022	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551403	Ndufs1	NADH:ubiquinone oxidoreductase core subunit S1	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20211021	MGI			
1551404	Wdr55	WD repeat domain 55	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15902260
1551405	Gpm6b	glycoprotein m6b	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0004143	muscle hypertonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0010205	abnormal oligodendrocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0010749	absent visual evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23322581
1551405	Gpm6b	glycoprotein m6b	gene	MP:0014740	increased auditory brainstem response wave peak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:23322581
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20221215	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20221215	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20221215	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20220811	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20221215	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0002809	increased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20221215	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20221215	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20221215	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20240523	MGI			
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0012705	increased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17589504
1551408	Ambra1	autophagy/beclin 1 regulator 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:17589504
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20181108	MGI			PMID:23754390
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987683
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987683
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:23754390
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0005077	abnormal melanogenesis		IAGP		N	RGD:5509061	20181108	MGI			PMID:23754390
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987683
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987683
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0009388	abnormal epidermal melanocyte morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:23754390
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0010192	abnormal retina melanin granule morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:23754390
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15987683
1551409	Bace2	beta-site APP-cleaving enzyme 2	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20210128	MGI			
1551410	Exoc8	exocyst complex component 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170105	MGI			
1551410	Exoc8	exocyst complex component 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551410	Exoc8	exocyst complex component 8	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:3875649
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117762
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20141003	MGI			PMID:2884254
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:805203
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634110
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:2884254
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:2884254
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001602	impaired myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117762
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8890160
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634110
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11449370
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7552994
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8890160
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371815
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:2884254
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7552994
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8890160
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3875649
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634110
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3875649
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117762
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618482
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:805203
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634110
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117762
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002467	impaired neutrophil phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117762
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002491	decreased IgD level		IEA		N	RGD:5509061	20111116	MGI			
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002493	increased IgG level		IEA		N	RGD:5509061	20111116	MGI			
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2884254
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0002497	increased IgE level		IEA		N	RGD:5509061	20111116	MGI			
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2884254
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117762
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371815
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634110
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:805203
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8890160
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117762
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618482
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:805203
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371815
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:805203
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842985
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20141003	MGI			
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371362
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7552994
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17105816
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634110
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8890160
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7552994
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8890160
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371815
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8890160
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008214	increased immature B cell number		IEA		N	RGD:5509061	20141003	MGI			
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8890160
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7552994
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008246	abnormal leukocyte morphology		IEA		N	RGD:5509061	20111116	MGI			
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11104803
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7552994
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8890160
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9371815
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008523	absent lymph node germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:9088978
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117762
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14634110
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2884254
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:805203
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842985
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17998386
1551411	Btk	Bruton agammaglobulinemia tyrosine kinase	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:15331445
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0000316	cellular necrosis		IAGP		N	RGD:5509061	20220616	MGI			PMID:34130995
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:34130995
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0000798	abnormal frontal lobe morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:34130995
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20201022	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20220616	MGI			PMID:34130995
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20220616	MGI			PMID:34130995
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220811	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25698751
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:34130995
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20241121	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25698751
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210128	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20220616	MGI			PMID:34130995
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0012448	abnormal primary motor cortex morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:34130995
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0015055	decreased synapse density		IAGP		N	RGD:5509061	20260813	MGI			PMID:25698751
1551412	Chmp2b	charged multivesicular body protein 2B	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20250508	MGI			
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20221215	MGI			
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19815013
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000829	dilated fourth ventricle		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314202
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19815013
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19815013
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20221215	MGI			
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314202
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20221215	MGI			
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314202
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19815013
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20221215	MGI			
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314202
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803037
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24055366
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314202
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314202
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:17314202
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314202
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19815013
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0010061	increased creatine level		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0010748	abnormal visual evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803037
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0010748	abnormal visual evoked potential		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314202
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17428816
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011634	abnormal mitochondrial inner membrane morphology		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24055366
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20652258
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20150611	MGI			PMID:21551073
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220811	MGI			
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20180802	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0014248	thin retina nerve fiber layer		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0014345	abnormal neuron mitochondrial morphology		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0014386	decreased muscle fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:23250881
1551416	Opa1	OPA1, mitochondrial dynamin like GTPase	gene	MP:0014392	increased neuron mitochondrial DNA content		IAGP		N	RGD:5509061	20260402	MGI			PMID:41706861
1551418	Rnd3	Rho family GTPase 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1551418	Rnd3	Rho family GTPase 3	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630292
1551418	Rnd3	Rho family GTPase 3	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630292
1551418	Rnd3	Rho family GTPase 3	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630292
1551418	Rnd3	Rho family GTPase 3	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0002200	abnormal brain ventricular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630292
1551418	Rnd3	Rho family GTPase 3	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0002958	cerebral aqueductal stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630292
1551418	Rnd3	Rho family GTPase 3	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0003358	abnormal hypaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0005356	positive geotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630292
1551418	Rnd3	Rho family GTPase 3	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20170105	MGI			
1551418	Rnd3	Rho family GTPase 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630292
1551418	Rnd3	Rho family GTPase 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0010152	abnormal brain ependyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630292
1551418	Rnd3	Rho family GTPase 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20201022	MGI			
1551418	Rnd3	Rho family GTPase 3	gene	MP:0020865	delayed suckling reflex loss		IAGP		N	RGD:5509061	20220922	MGI			PMID:21552537
1551418	Rnd3	Rho family GTPase 3	gene	MP:0021165	behavioral developmental delay		IAGP		N	RGD:5509061	20220922	MGI			PMID:21552537
1551421	Angel1	angel homolog 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20200310	MGI			
1551421	Angel1	angel homolog 1	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20200310	MGI			
1551421	Angel1	angel homolog 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20200310	MGI			
1551423	Rnf113a1	ring finger protein 113A1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0001148	enlarged testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20150326	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263735
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263735
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20141003	MGI			
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0008891	decreased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263735
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0009906	increased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010266	decreased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18263735
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010278	increased glioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010346	increased thyroid carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010366	increased adrenal cortical tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010384	increased renal carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010503	myocardial trabeculae hypoplasia		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010561	absent coronary vessels		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0010733	abnormal axon initial segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22632975
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22632975
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12543979
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0011392	increased fetal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0013309	adrenal gland cyst		IAGP		N	RGD:5509061	20141120	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0013328	visceromegaly		IAGP		N	RGD:5509061	20141204	MGI			PMID:20739274
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0020135	abnormal heart ventricle wall thickness		IAGP		N	RGD:5509061	20151112	MGI			PMID:24064296
1551425	Sptbn1	spectrin beta, non-erythrocytic 1	gene	MP:0031525	thin left ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:24064296
1551426	Trim42	tripartite motif-containing 42	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20260402	MGI			
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20220519	MGI			
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20220519	MGI			
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20211021	MGI			
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0014658	absent a-wave		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0020439	absent b-wave		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551428	Iqcb1	IQ calmodulin-binding motif containing 1	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20251016	MGI			PMID:27328943
1551429	Ccl11	C-C motif chemokine ligand 11	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16210640
1551429	Ccl11	C-C motif chemokine ligand 11	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16210640
1551429	Ccl11	C-C motif chemokine ligand 11	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
1551429	Ccl11	C-C motif chemokine ligand 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9808585
1551429	Ccl11	C-C motif chemokine ligand 11	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17060636
1551429	Ccl11	C-C motif chemokine ligand 11	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9034156
1551429	Ccl11	C-C motif chemokine ligand 11	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20150402	MGI			PMID:16210640
1551429	Ccl11	C-C motif chemokine ligand 11	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9034156
1551430	Skic8	SKI8 subunit of superkiller complex	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1551430	Skic8	SKI8 subunit of superkiller complex	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1551430	Skic8	SKI8 subunit of superkiller complex	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20240523	MGI			
1551430	Skic8	SKI8 subunit of superkiller complex	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1551430	Skic8	SKI8 subunit of superkiller complex	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1551430	Skic8	SKI8 subunit of superkiller complex	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1551430	Skic8	SKI8 subunit of superkiller complex	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505249
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19221053
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20503133
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:22231481
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:8893006
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:14499482
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10727705
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001968	abnormal touch/nociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:12525693
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835636
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:8893006
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:9037090
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:21232580
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001980	abnormal chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:21957251
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:18207746
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:21957251
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:19273844
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:19528658
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:21232580
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:9555078
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19221053
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:12525693
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20200310	MGI			PMID:15926936
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:15355329
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:10727705
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19221053
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835636
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15893889
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0003959	abnormal lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:19221053
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:10515257
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:19528658
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:9037090
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19221053
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19221053
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0006001	abnormal intestinal transit time		IAGP		N	RGD:5509061	20200310	MGI			PMID:19273844
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:17544222
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:11377918
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:21232580
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:24069332
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:15355329
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19221053
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20200310	MGI			PMID:19221053
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:19528658
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009713	enhanced conditioned place preference behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:11377918
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18207746
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009748	abnormal behavioral response to addictive substance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24069332
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15355329
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009753	enhanced behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:21957251
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20200310	MGI			PMID:12781916
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:10195199
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:10515257
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:11032994
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:11377918
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:12781916
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:17544222
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:19528658
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:21232580
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:24069332
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:8893006
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009757	impaired behavioral response to morphine		IAGP		N	RGD:5509061	20200310	MGI			PMID:9555078
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:11377918
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:9555078
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009776	decreased behavioral withdrawal response		IAGP		N	RGD:5509061	20200310	MGI			PMID:10835636
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009778	impaired behavioral response to anesthetic		IAGP		N	RGD:5509061	20200310	MGI			PMID:10195199
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009778	impaired behavioral response to anesthetic		IAGP		N	RGD:5509061	20200310	MGI			PMID:11032994
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009778	impaired behavioral response to anesthetic		IAGP		N	RGD:5509061	20200310	MGI			PMID:17544222
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0009779	enhanced behavioral response to anesthetic		IAGP		N	RGD:5509061	20200310	MGI			PMID:11032994
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:19221053
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0030982	abnormal copulatory plug deposition		IAGP		N	RGD:5509061	20240718	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0031436	decreased copulatory plug deposition		IAGP		N	RGD:5509061	20240718	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0031628	abnormal intromission		IAGP		N	RGD:5509061	20240718	MGI			PMID:9126934
1551432	Oprm1	opioid receptor, mu 1	gene	MP:0031650	decreased mounting behavior		IAGP		N	RGD:5509061	20240905	MGI			PMID:9126934
1551433	Ntn3	netrin 3	gene	MP:0003177	allodynia		IAGP		N	RGD:5509061	20230921	MGI			PMID:36587114
1551433	Ntn3	netrin 3	gene	MP:0014488	abnormal skin sensory neuron innervation pattern		IAGP		N	RGD:5509061	20240801	MGI			PMID:36587114
1551433	Ntn3	netrin 3	gene	MP:0020954	decreased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20230921	MGI			PMID:36587114
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:27618312
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27618312
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:27618312
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0011724	ectopic cortical neuron		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0013227	small brain ventricles		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0020388	decreased radial glial cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0020392	abnormal radial glial cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551436	Rbm8a	RNA binding motif protein 8a	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25948253
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0004650	increased lumbar vertebrae number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0004651	increased thoracic vertebrae number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24019467
1551437	Wfikkn2	WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2	gene	MP:0021206	abnormal limb muscle morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:24019467
1551442	Zhx2	zinc fingers and homeoboxes 2	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:67170
1551444	Rbm34	RNA binding motif protein 34	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1551445	Rnase11	ribonuclease, RNase A family, 11 (non-active)	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1551445	Rnase11	ribonuclease, RNase A family, 11 (non-active)	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1551445	Rnase11	ribonuclease, RNase A family, 11 (non-active)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1551445	Rnase11	ribonuclease, RNase A family, 11 (non-active)	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20241121	MGI			
1551445	Rnase11	ribonuclease, RNase A family, 11 (non-active)	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1551445	Rnase11	ribonuclease, RNase A family, 11 (non-active)	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1551445	Rnase11	ribonuclease, RNase A family, 11 (non-active)	gene	MP:0003918	decreased kidney weight		IEA		N	RGD:5509061	20210826	MGI			
1551445	Rnase11	ribonuclease, RNase A family, 11 (non-active)	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1551445	Rnase11	ribonuclease, RNase A family, 11 (non-active)	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20210520	MGI			
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15003629
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11696558
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:29180569
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0003334	pancreas fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11696558
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0003335	exocrine pancreatic insufficiency		IAGP		N	RGD:5509061	20200310	MGI			PMID:11696558
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15003629
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11696558
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16645041
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:22510200
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0008780	increased pancreatic acinar cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009043	increased pancreas adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11696558
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12829745
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22510200
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009147	abnormal pancreatic acinar cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22510200
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19028870
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009155	pancreatic acinar hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009160	abnormal pancreatic acinar cell zymogen granule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11696558
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009160	abnormal pancreatic acinar cell zymogen granule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15003629
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009160	abnormal pancreatic acinar cell zymogen granule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22510200
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16645041
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0010172	abnormal mammary gland epithelium physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16645041
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0013184	hemorrhagic ascites		IAGP		N	RGD:5509061	20200310	MGI			PMID:16397237
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0013317	abnormal seminal vesicle development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17901072
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0013594	abnormal parotid gland acinus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15003629
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0013781	abnormal mammary gland luminal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16645041
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0013899	abnormal seminal vesicle epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17901072
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0013900	seminal vesicle epithelium degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:17901072
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0013903	abnormal seminal vesicle fluid composition		IAGP		N	RGD:5509061	20200310	MGI			PMID:17901072
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0014098	decreased pancreatic amylase secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22510200
1551446	Bhlha15	basic helix-loop-helix family, member a15	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16645041
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17455169
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20210826	MGI			
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372036
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147852
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372036
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147852
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593193
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200220	MGI			PMID:19533782
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17455169
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200220	MGI			PMID:19533782
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17455169
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372036
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17455169
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593193
1551450	Jam3	junction adhesion molecule 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372036
1551450	Jam3	junction adhesion molecule 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200220	MGI			PMID:19533782
1551450	Jam3	junction adhesion molecule 3	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17455169
1551450	Jam3	junction adhesion molecule 3	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372036
1551450	Jam3	junction adhesion molecule 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17455169
1551450	Jam3	junction adhesion molecule 3	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15372036
1551450	Jam3	junction adhesion molecule 3	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0004545	enlarged esophagus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17455169
1551450	Jam3	junction adhesion molecule 3	gene	MP:0004545	enlarged esophagus		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0004545	enlarged esophagus		IAGP		N	RGD:5509061	20200220	MGI			PMID:19533782
1551450	Jam3	junction adhesion molecule 3	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147852
1551450	Jam3	junction adhesion molecule 3	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20200220	MGI			PMID:19533782
1551450	Jam3	junction adhesion molecule 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200220	MGI			PMID:19533782
1551450	Jam3	junction adhesion molecule 3	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147852
1551450	Jam3	junction adhesion molecule 3	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17455169
1551450	Jam3	junction adhesion molecule 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593193
1551450	Jam3	junction adhesion molecule 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593193
1551450	Jam3	junction adhesion molecule 3	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20220811	MGI			
1551450	Jam3	junction adhesion molecule 3	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1551450	Jam3	junction adhesion molecule 3	gene	MP:0013891	increased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20200220	MGI			PMID:19109565
1551450	Jam3	junction adhesion molecule 3	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:21147852
1551450	Jam3	junction adhesion molecule 3	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20161013	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:21147852
1551450	Jam3	junction adhesion molecule 3	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:23029139
1551450	Jam3	junction adhesion molecule 3	gene	MP:0031109	subarachnoid hemorrhage		IAGP		N	RGD:5509061	20200910	MGI			PMID:23029139
1551451	Arl5a	ADP-ribosylation factor-like 5A	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1551451	Arl5a	ADP-ribosylation factor-like 5A	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20210128	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20200310	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210128	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20200310	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20200310	MGI			
1551453	Tbc1d22a	TBC1 domain family, member 22a	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1551454	Plbd2	phospholipase B domain containing 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1551454	Plbd2	phospholipase B domain containing 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20250508	MGI			
1551454	Plbd2	phospholipase B domain containing 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230601	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0011922	abnormal circulating osteocalcin level		IAGP		N	RGD:5509061	20181004	MGI			PMID:25753038
1551455	Vkorc1l1	vitamin K epoxide reductase complex, subunit 1-like 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0010752	impaired mucociliary clearance		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551456	Zmynd10	zinc finger, MYND domain containing 10	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20180712	MGI			PMID:29601588
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200310	MGI			
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20200310	MGI			
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26950939
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:26950939
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0003405	abnormal platelet shape		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0012197	impaired myofibroblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0020399	enhanced megakaryocyte emperipolesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0020399	enhanced megakaryocyte emperipolesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26950939
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0020431	decreased platelet alpha-granule number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863626
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0020431	decreased platelet alpha-granule number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25258341
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0020431	decreased platelet alpha-granule number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26950939
1551459	Nbeal2	neurobeachin-like 2	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:23863626
1551460	Mkrn1	makorin, ring finger protein, 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16882727
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075059
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0001770	abnormal iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075058
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:21748766
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21748766
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0002810	microcytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075058
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075059
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21748766
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0005638	hemochromatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075058
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0005638	hemochromatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075059
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0005638	hemochromatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21748766
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075058
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075059
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21748766
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075058
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075059
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21748766
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075059
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21748766
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075059
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0011890	increased circulating ferritin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21748766
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0011897	decreased circulating unsaturated transferrin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21748766
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0013302	increased pancreas iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075058
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0013302	increased pancreas iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0013303	decreased pancreas iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0020367	increased heart iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16075058
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0020367	increased heart iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0020368	decreased heart iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220811	MGI			
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0031692	decreased muscle iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:20200349
1551463	Hjv	hemojuvelin BMP co-receptor	gene	MP:0031693	increased muscle iron level		IAGP		N	RGD:5509061	20260219	MGI			PMID:20200349
1551466	Arcn1	archain 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12955145
1551466	Arcn1	archain 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0003214	neurofibrillary tangles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12955145
1551466	Arcn1	archain 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0008733	abnormal hair shaft melanin granule distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0009992	abnormal cerebellum vermis lobule IX morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0009994	abnormal cerebellum vermis lobule VI morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0009995	abnormal cerebellum vermis lobule VII morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0009997	abnormal cerebellum vermis lobule X morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502676
1551466	Arcn1	archain 1	gene	MP:0030949	abnormal Golgi vesicle transport		IAGP		N	RGD:5509061	20190725	MGI			PMID:20502676
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761531
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:3410303
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:6322428
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20230601	MGI			
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761531
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6322428
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0002095	abnormal skin pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090228
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17384153
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0002877	abnormal melanocyte morphology		IEA		N	RGD:5509061	20111116	MGI			
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0003798	abnormal Harderian gland pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0004721	abnormal platelet dense granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070017
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859366
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070017
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17062724
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17384153
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266473
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266472
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266473
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17090228
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:10859366
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070017
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0008327	abnormal corticotroph morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761531
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:11228153
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0008790	abnormal NK cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11266473
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0008791	decreased NK cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0008834	abnormal melanosome transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:11228153
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070017
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17384153
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070017
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070017
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17384153
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0009557	decreased platelet ADP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070017
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0010809	abnormal club cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21160031
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21160031
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0010943	abnormal bronchus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21160031
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:10859366
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:12070017
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:17384153
1551470	Rab27a	RAB27A, member RAS oncogene family	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23160464
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20230601	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0000603	pale liver		IEA		N	RGD:5509061	20230601	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230119	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:21778431
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230119	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20230119	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20230119	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21778431
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230119	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0010194	absent lymphatic vessels		IAGP		N	RGD:5509061	20200310	MGI			PMID:21778431
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0010194	absent lymphatic vessels		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21778431
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1551471	Ccbe1	collagen and calcium binding EGF domains 1	gene	MP:0011243	decreased fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23426945
1551477	Sall3	spalt like transcription factor 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0000959	abnormal somatic sensory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0003154	abnormal soft palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20250508	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0010371	abnormal epiglottis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20260402	MGI			
1551477	Sall3	spalt like transcription factor 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282310
1551477	Sall3	spalt like transcription factor 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1551480	Rfc2	replication factor C (activator 1) 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551480	Rfc2	replication factor C (activator 1) 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551486	Map3k2	mitogen-activated protein kinase kinase kinase 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12138187
1551486	Map3k2	mitogen-activated protein kinase kinase kinase 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23125215
1551486	Map3k2	mitogen-activated protein kinase kinase kinase 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12138187
1551486	Map3k2	mitogen-activated protein kinase kinase kinase 2	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23125215
1551486	Map3k2	mitogen-activated protein kinase kinase kinase 2	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12138187
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551487	Samsn1	SAM domain, SH3 domain and nuclear localization signals, 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923443
1551490	Fndc7	fibronectin type III domain containing 7	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1551490	Fndc7	fibronectin type III domain containing 7	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1551490	Fndc7	fibronectin type III domain containing 7	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
1551493	Ddx24	DEAD box helicase 24	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20210128	MGI			
1551493	Ddx24	DEAD box helicase 24	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210128	MGI			
1551493	Ddx24	DEAD box helicase 24	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1551493	Ddx24	DEAD box helicase 24	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1551493	Ddx24	DEAD box helicase 24	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180315	MGI			PMID:24204270
1551493	Ddx24	DEAD box helicase 24	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20180315	MGI			PMID:24204270
1551493	Ddx24	DEAD box helicase 24	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551493	Ddx24	DEAD box helicase 24	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1551493	Ddx24	DEAD box helicase 24	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1551493	Ddx24	DEAD box helicase 24	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:24204270
1551494	Hsdl2	hydroxysteroid dehydrogenase like 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0000341	abnormal bile color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12429862
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20201231	MGI			
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20151224	MGI			PMID:22473008
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150101	MGI			PMID:22134889
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546952
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:21881209
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0004147	increased porphyrin level		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12429862
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0005653	phototoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12429862
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0005654	porphyria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12429862
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0008055	increased urine osmolality		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20151224	MGI			PMID:22473008
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15546952
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0009810	increased urine uric acid level		IAGP		N	RGD:5509061	20151224	MGI			PMID:22473008
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20210812	MGI			PMID:32488095
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:23954234
1551496	Abcg2	ATP binding cassette subfamily G member 2 (Junior blood group)	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:23954234
1551497	Kazn	kazrin, periplakin interacting protein	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1551497	Kazn	kazrin, periplakin interacting protein	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1551497	Kazn	kazrin, periplakin interacting protein	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1551497	Kazn	kazrin, periplakin interacting protein	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1551499	Caskin1	CASK interacting protein 1	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1551499	Caskin1	CASK interacting protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1551499	Caskin1	CASK interacting protein 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20210603	MGI			PMID:31727973
1551499	Caskin1	CASK interacting protein 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170105	MGI			
1551499	Caskin1	CASK interacting protein 1	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1551499	Caskin1	CASK interacting protein 1	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20210603	MGI			PMID:31727973
1551499	Caskin1	CASK interacting protein 1	gene	MP:0003908	decreased stereotypic behavior		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0005407	hyperalgesia		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1551499	Caskin1	CASK interacting protein 1	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0009455	enhanced cued conditioning behavior		IAGP		N	RGD:5509061	20191107	MGI			PMID:30359304
1551499	Caskin1	CASK interacting protein 1	gene	MP:0010378	increased respiratory quotient		IEA		N	RGD:5509061	20220519	MGI			
1551499	Caskin1	CASK interacting protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551499	Caskin1	CASK interacting protein 1	gene	MP:0011625	cystolithiasis		IEA		N	RGD:5509061	20170105	MGI			
1551499	Caskin1	CASK interacting protein 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20210603	MGI			PMID:31727973
1551499	Caskin1	CASK interacting protein 1	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:31727973
1551499	Caskin1	CASK interacting protein 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:30359304
1551501	Gpr108	G protein-coupled receptor 108	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20200514	MGI			
1551501	Gpr108	G protein-coupled receptor 108	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1551501	Gpr108	G protein-coupled receptor 108	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20190103	MGI			PMID:30332431
1551501	Gpr108	G protein-coupled receptor 108	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20190103	MGI			PMID:30332431
1551501	Gpr108	G protein-coupled receptor 108	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20190103	MGI			PMID:30332431
1551501	Gpr108	G protein-coupled receptor 108	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20190103	MGI			PMID:30332431
1551501	Gpr108	G protein-coupled receptor 108	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20190103	MGI			PMID:30332431
1551501	Gpr108	G protein-coupled receptor 108	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
1551502	Ppp1r10	protein phosphatase 1, regulatory subunit 10	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1551503	Hrnr	hornerin	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20201022	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20230601	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20231207	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20230601	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0002581	abnormal ileum morphology		IEA		N	RGD:5509061	20231207	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20260402	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0003271	abnormal duodenum morphology		IEA		N	RGD:5509061	20231207	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20241121	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20250508	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1551504	Ak4	adenylate kinase 4	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20241121	MGI			
1551505	Hhipl1	hedgehog interacting protein-like 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20160811	MGI			
1551505	Hhipl1	hedgehog interacting protein-like 1	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20221215	MGI			
1551505	Hhipl1	hedgehog interacting protein-like 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20201217	MGI			PMID:31163988
1551505	Hhipl1	hedgehog interacting protein-like 1	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31163988
1551505	Hhipl1	hedgehog interacting protein-like 1	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20201217	MGI			PMID:31163988
1551505	Hhipl1	hedgehog interacting protein-like 1	gene	MP:0031509	decreased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:31163988
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20201022	MGI			PMID:30905411
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20241121	MGI			
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20201022	MGI			PMID:30905411
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20250130	MGI			PMID:39088537
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20250130	MGI			PMID:39088537
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:30905411
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:39088537
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:39088537
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20201022	MGI			PMID:30905411
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20250130	MGI			PMID:39088537
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250130	MGI			PMID:39088537
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20201022	MGI			PMID:30905411
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20250130	MGI			PMID:39088537
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20201022	MGI			PMID:30905411
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0030798	joint contracture		IAGP		N	RGD:5509061	20250130	MGI			PMID:39088537
1551507	Plod2	procollagen lysine, 2-oxoglutarate 5-dioxygenase 2	gene	MP:0030800	abnormal patellar ligament morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:39088537
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20231207	MGI			
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32265257
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32265257
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32265257
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32265257
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0008455	abnormal retina rod cell inner segment morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20210506	MGI			PMID:32265257
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551510	Impg2	interphotoreceptor matrix proteoglycan 2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20201029	MGI			PMID:32242237
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000532	kidney vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1551511	Ccn3	cellular communication network factor 3	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1551511	Ccn3	cellular communication network factor 3	gene	MP:0001268	barrel chest		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1551511	Ccn3	cellular communication network factor 3	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0001506	limp posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1551511	Ccn3	cellular communication network factor 3	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
1551511	Ccn3	cellular communication network factor 3	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0002952	ventricular cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1551511	Ccn3	cellular communication network factor 3	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0003808	increased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0004695	increased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20139355
1551511	Ccn3	cellular communication network factor 3	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0006137	venoocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0008069	abnormal joint mobility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19934377
1551511	Ccn3	cellular communication network factor 3	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0030796	hip dislocation		IAGP		N	RGD:5509061	20181011	MGI			PMID:18289368
1551511	Ccn3	cellular communication network factor 3	gene	MP:0031510	increased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:20139355
1551512	Eif3d	eukaryotic translation initiation factor 3, subunit D	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20260402	MGI			
1551512	Eif3d	eukaryotic translation initiation factor 3, subunit D	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1551512	Eif3d	eukaryotic translation initiation factor 3, subunit D	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20260402	MGI			
1551512	Eif3d	eukaryotic translation initiation factor 3, subunit D	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20260402	MGI			
1551512	Eif3d	eukaryotic translation initiation factor 3, subunit D	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1551513	Txndc12	thioredoxin domain containing 12 (endoplasmic reticulum)	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20200310	MGI			
1551516	Cc2d1b	coiled-coil and C2 domain containing 1B	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20200310	MGI			
1551516	Cc2d1b	coiled-coil and C2 domain containing 1B	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1551516	Cc2d1b	coiled-coil and C2 domain containing 1B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201015	MGI			PMID:26720614
1551516	Cc2d1b	coiled-coil and C2 domain containing 1B	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20200310	MGI			
1551516	Cc2d1b	coiled-coil and C2 domain containing 1B	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200310	MGI			
1551519	Prss27	serine protease 27	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1551519	Prss27	serine protease 27	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23447538
1551520	Keg1	kidney expressed gene 1	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1551520	Keg1	kidney expressed gene 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1551520	Keg1	kidney expressed gene 1	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1551520	Keg1	kidney expressed gene 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1551520	Keg1	kidney expressed gene 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1551520	Keg1	kidney expressed gene 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201022	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210520	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20201022	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20201022	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551523	Ddx39a	DEAD box helicase 39a	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20201022	MGI			
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0014394	increased skeletal muscle fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240328	MGI			PMID:19490905
1551524	Mterf2	mitochondrial transcription termination factor 2	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20200310	MGI			PMID:19490905
1551526	Fads3	fatty acid desaturase 3	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1551526	Fads3	fatty acid desaturase 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1551526	Fads3	fatty acid desaturase 3	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28838557
1551526	Fads3	fatty acid desaturase 3	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28838557
1551526	Fads3	fatty acid desaturase 3	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20181227	MGI			
1551526	Fads3	fatty acid desaturase 3	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28838557
1551526	Fads3	fatty acid desaturase 3	gene	MP:0010360	decreased liver free fatty acids level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28838557
1551528	Sap18	Sin3A-associated polypeptide 18	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1551528	Sap18	Sin3A-associated polypeptide 18	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551528	Sap18	Sin3A-associated polypeptide 18	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551529	Phf19	PHD finger protein 19	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:32821835
1551529	Phf19	PHD finger protein 19	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20211209	MGI			PMID:32821835
1551529	Phf19	PHD finger protein 19	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20211209	MGI			PMID:32821835
1551529	Phf19	PHD finger protein 19	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210805	MGI			
1551529	Phf19	PHD finger protein 19	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210805	MGI			
1551529	Phf19	PHD finger protein 19	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20211209	MGI			PMID:32821835
1551529	Phf19	PHD finger protein 19	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210805	MGI			
1551529	Phf19	PHD finger protein 19	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20211209	MGI			PMID:32821835
1551529	Phf19	PHD finger protein 19	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210805	MGI			
1551529	Phf19	PHD finger protein 19	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20231207	MGI			
1551529	Phf19	PHD finger protein 19	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20211209	MGI			PMID:32821835
1551529	Phf19	PHD finger protein 19	gene	MP:0011181	increased hematopoietic cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:32821835
1551529	Phf19	PHD finger protein 19	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20211209	MGI			PMID:32821835
1551529	Phf19	PHD finger protein 19	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20211209	MGI			PMID:32821835
1551530	Rchy1	ring finger and CHY zinc finger domain containing 1	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21791603
1551532	Cd99l2	CD99 antigen-like 2	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293350
1551532	Cd99l2	CD99 antigen-like 2	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293350
1551533	Cd248	CD248 antigen, endosialin	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20200310	MGI			
1551533	Cd248	CD248 antigen, endosialin	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210520	MGI			
1551533	Cd248	CD248 antigen, endosialin	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20200310	MGI			
1551533	Cd248	CD248 antigen, endosialin	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1551533	Cd248	CD248 antigen, endosialin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:21402174
1551533	Cd248	CD248 antigen, endosialin	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16492758
1551534	Pdia4	protein disulfide isomerase associated 4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1551534	Pdia4	protein disulfide isomerase associated 4	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20200402	MGI			
1551534	Pdia4	protein disulfide isomerase associated 4	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20200310	MGI			PMID:28576878
1551534	Pdia4	protein disulfide isomerase associated 4	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28576878
1551534	Pdia4	protein disulfide isomerase associated 4	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28576878
1551534	Pdia4	protein disulfide isomerase associated 4	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1551535	Atp5mg	ATP synthase membrane subunit g	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230720	MGI			
1551535	Atp5mg	ATP synthase membrane subunit g	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230720	MGI			
1551535	Atp5mg	ATP synthase membrane subunit g	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20230720	MGI			
1551535	Atp5mg	ATP synthase membrane subunit g	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20230720	MGI			
1551535	Atp5mg	ATP synthase membrane subunit g	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20230720	MGI			
1551535	Atp5mg	ATP synthase membrane subunit g	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230720	MGI			
1551535	Atp5mg	ATP synthase membrane subunit g	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230720	MGI			
1551535	Atp5mg	ATP synthase membrane subunit g	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230720	MGI			
1551541	Plekhn1	pleckstrin homology domain containing N1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20211028	MGI			PMID:27616329
1551541	Plekhn1	pleckstrin homology domain containing N1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20211028	MGI			PMID:27616329
1551541	Plekhn1	pleckstrin homology domain containing N1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20211028	MGI			PMID:27616329
1551541	Plekhn1	pleckstrin homology domain containing N1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20211028	MGI			PMID:27616329
1551541	Plekhn1	pleckstrin homology domain containing N1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20211028	MGI			PMID:27616329
1551541	Plekhn1	pleckstrin homology domain containing N1	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20211028	MGI			PMID:27616329
1551541	Plekhn1	pleckstrin homology domain containing N1	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20211028	MGI			PMID:27616329
1551541	Plekhn1	pleckstrin homology domain containing N1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20211028	MGI			PMID:27616329
1551541	Plekhn1	pleckstrin homology domain containing N1	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20211028	MGI			PMID:27616329
1551542	Chd6	chromodomain helicase DNA binding protein 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20111866
1551542	Chd6	chromodomain helicase DNA binding protein 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1551542	Chd6	chromodomain helicase DNA binding protein 6	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:20111866
1551542	Chd6	chromodomain helicase DNA binding protein 6	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20111866
1551542	Chd6	chromodomain helicase DNA binding protein 6	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20231207	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551544	Kif6	kinesin family member 6	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551544	Kif6	kinesin family member 6	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551544	Kif6	kinesin family member 6	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551544	Kif6	kinesin family member 6	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551544	Kif6	kinesin family member 6	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551544	Kif6	kinesin family member 6	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551544	Kif6	kinesin family member 6	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551544	Kif6	kinesin family member 6	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551544	Kif6	kinesin family member 6	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20260402	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230601	MGI			
1551544	Kif6	kinesin family member 6	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:30475797
1551546	Foxi2	forkhead box I2	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:26550799
1551546	Foxi2	forkhead box I2	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:26550799
1551546	Foxi2	forkhead box I2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180215	MGI			PMID:26550799
1551546	Foxi2	forkhead box I2	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:26550799
1551546	Foxi2	forkhead box I2	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20180215	MGI			PMID:26550799
1551546	Foxi2	forkhead box I2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0020223	increased alertness		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0030973	impaired gluconeogenesis		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551547	Or10p1	olfactory receptor family 10 subfamily P member 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20250515	MGI			PMID:36806353
1551549	Angpt1	angiopoietin 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21606590
1551549	Angpt1	angiopoietin 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20200310	MGI			PMID:8980224
1551549	Angpt1	angiopoietin 1	gene	MP:0000264	failure of vascular branching		IAGP		N	RGD:5509061	20200310	MGI			PMID:8980224
1551549	Angpt1	angiopoietin 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21606590
1551549	Angpt1	angiopoietin 1	gene	MP:0000293	absent myocardial trabeculae		IAGP		N	RGD:5509061	20200310	MGI			PMID:8980224
1551549	Angpt1	angiopoietin 1	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21606590
1551549	Angpt1	angiopoietin 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20200310	MGI			PMID:24048525
1551549	Angpt1	angiopoietin 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8980224
1551549	Angpt1	angiopoietin 1	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8980224
1551549	Angpt1	angiopoietin 1	gene	MP:0004226	absent Schlemm's canal		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21606590
1551549	Angpt1	angiopoietin 1	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0005257	abnormal intraocular pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21606590
1551549	Angpt1	angiopoietin 1	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20230810	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8980224
1551549	Angpt1	angiopoietin 1	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8980224
1551549	Angpt1	angiopoietin 1	gene	MP:0006149	decreased visual acuity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20200310	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24048525
1551549	Angpt1	angiopoietin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21606590
1551549	Angpt1	angiopoietin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:8980224
1551549	Angpt1	angiopoietin 1	gene	MP:0012049	increased susceptilbility to retina ischemic injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:24048525
1551549	Angpt1	angiopoietin 1	gene	MP:0012066	decreased astrocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24048525
1551549	Angpt1	angiopoietin 1	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20200310	MGI			PMID:8980224
1551549	Angpt1	angiopoietin 1	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:25202984
1551549	Angpt1	angiopoietin 1	gene	MP:0031500	increased cornea size		IAGP		N	RGD:5509061	20230810	MGI			PMID:25202984
1551552	Adss2	adenylosuccinate synthase 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1551552	Adss2	adenylosuccinate synthase 2	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1551552	Adss2	adenylosuccinate synthase 2	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20231207	MGI			
1551552	Adss2	adenylosuccinate synthase 2	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1551552	Adss2	adenylosuccinate synthase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1551552	Adss2	adenylosuccinate synthase 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
1551552	Adss2	adenylosuccinate synthase 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20231207	MGI			
1551553	Polr2f	polymerase (RNA) II (DNA directed) polypeptide F	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1551555	Ptgr2	prostaglandin reductase 2	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1551555	Ptgr2	prostaglandin reductase 2	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1551556	P4ha3	procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide III	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0009596	abnormal stratum corneum lipid matrix formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551559	Slurp1	secreted Ly6/Plaur domain containing 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:24499735
1551560	Hpcal4	hippocalcin-like 4	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1551560	Hpcal4	hippocalcin-like 4	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200409	MGI			PMID:32015563
1551560	Hpcal4	hippocalcin-like 4	gene	MP:0005631	decreased lung weight		IEA		N	RGD:5509061	20201022	MGI			
1551562	Crbn	cereblon	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210128	MGI			
1551562	Crbn	cereblon	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20210128	MGI			
1551562	Crbn	cereblon	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20190718	MGI			PMID:29459374
1551562	Crbn	cereblon	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1551562	Crbn	cereblon	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20190718	MGI			PMID:29459374
1551562	Crbn	cereblon	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1551562	Crbn	cereblon	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23349485
1551562	Crbn	cereblon	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21995942
1551562	Crbn	cereblon	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20190718	MGI			PMID:29459374
1551562	Crbn	cereblon	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:29459374
1551562	Crbn	cereblon	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20190718	MGI			PMID:29459374
1551562	Crbn	cereblon	gene	MP:0013660	abnormal bone marrow hematopoietic cell morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20190314	MGI			PMID:30064974
1551562	Crbn	cereblon	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:23349485
1551563	Cand2	cullin associated and neddylation dissociated 2 (putative)	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200310	MGI			
1551563	Cand2	cullin associated and neddylation dissociated 2 (putative)	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1551563	Cand2	cullin associated and neddylation dissociated 2 (putative)	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20260122	MGI			PMID:34605609
1551563	Cand2	cullin associated and neddylation dissociated 2 (putative)	gene	MP:0005478	decreased circulating thyroxine level		IEA		N	RGD:5509061	20211021	MGI			
1551563	Cand2	cullin associated and neddylation dissociated 2 (putative)	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1551563	Cand2	cullin associated and neddylation dissociated 2 (putative)	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1551567	Glud1	glutamate dehydrogenase 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19015267
1551567	Glud1	glutamate dehydrogenase 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19015267
1551567	Glud1	glutamate dehydrogenase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19015267
1551567	Glud1	glutamate dehydrogenase 1	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20200310	MGI			PMID:19015267
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0000519	hydronephrosis		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0003675	kidney cyst		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20200310	MGI			
1551568	Pigv	phosphatidylinositol glycan anchor biosynthesis, class V	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20200310	MGI			
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0001128	ovary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551569	Pcyt1b	phosphate cytidylyltransferase 1, choline, beta isoform	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15143167
1551573	Ascc1	activating signal cointegrator 1 complex subunit 1	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20220519	MGI			
1551573	Ascc1	activating signal cointegrator 1 complex subunit 1	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20200402	MGI			
1551573	Ascc1	activating signal cointegrator 1 complex subunit 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551573	Ascc1	activating signal cointegrator 1 complex subunit 1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1551573	Ascc1	activating signal cointegrator 1 complex subunit 1	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20220811	MGI			
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210318	MGI			PMID:33569080
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20210318	MGI			PMID:33569080
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:33569080
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:33569080
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:33569080
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20241121	MGI			
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20210318	MGI			PMID:33569080
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20250508	MGI			
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20210318	MGI			PMID:33569080
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20210318	MGI			PMID:33569080
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0012165	absent neural folds		IAGP		N	RGD:5509061	20210318	MGI			PMID:33569080
1551580	Gcsh	glycine cleavage system protein H (aminomethyl carrier)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551581	Slc4a8	solute carrier family 4 (anion exchanger), member 8	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1551581	Slc4a8	solute carrier family 4 (anion exchanger), member 8	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1551581	Slc4a8	solute carrier family 4 (anion exchanger), member 8	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20389022
1551581	Slc4a8	solute carrier family 4 (anion exchanger), member 8	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20389022
1551587	Sec24c	SEC24 homolog C, COPII coat complex component	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:24876386
1551587	Sec24c	SEC24 homolog C, COPII coat complex component	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24876386
1551587	Sec24c	SEC24 homolog C, COPII coat complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24876386
1551588	Tmem63c	transmembrane protein 63c	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1551588	Tmem63c	transmembrane protein 63c	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1551588	Tmem63c	transmembrane protein 63c	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1551588	Tmem63c	transmembrane protein 63c	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20210520	MGI			
1551588	Tmem63c	transmembrane protein 63c	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210520	MGI			
1551588	Tmem63c	transmembrane protein 63c	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1551589	Spg7	SPG7, paraplegin matrix AAA peptidase subunit	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722615
1551589	Spg7	SPG7, paraplegin matrix AAA peptidase subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722615
1551589	Spg7	SPG7, paraplegin matrix AAA peptidase subunit	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722615
1551589	Spg7	SPG7, paraplegin matrix AAA peptidase subunit	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722615
1551589	Spg7	SPG7, paraplegin matrix AAA peptidase subunit	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722615
1551589	Spg7	SPG7, paraplegin matrix AAA peptidase subunit	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722615
1551589	Spg7	SPG7, paraplegin matrix AAA peptidase subunit	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722615
1551589	Spg7	SPG7, paraplegin matrix AAA peptidase subunit	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722615
1551589	Spg7	SPG7, paraplegin matrix AAA peptidase subunit	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14722615
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000380	small hair follicles		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230601	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230601	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001512	trunk curl		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20220811	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20220811	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20181227	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002965	increased circulating serum albumin level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20220811	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0004473	absent nasal bone		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0004757	abnormal distal convoluted tubule morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0004791	absent lower incisors		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005367	renal/urinary system phenotype		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005507	tail dragging		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005540	decreased urine albumin level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20230601	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20231207	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0008806	increased circulating amylase level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0009051	dilated distal convoluted tubule		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0010234	abnormal vibrissa follicle morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0011424	decreased urine uric acid level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0011435	increased urine magnesium level		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0011585	decreased alkaline phosphatase activity		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20210304	MGI			PMID:28818080
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0012121	sclerocornea		IEA		N	RGD:5509061	20230601	MGI			
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0012725	small sebaceous gland		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0013370	anhidrosis		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0013458	decreased eccrine gland number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0030178	abnormal scalp morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551590	Kctd1	potassium channel tetramerisation domain containing 1	gene	MP:0031449	abnormal nasal cartilage morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38113115
1551591	Gpr173	G-protein coupled receptor 173	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1551591	Gpr173	G-protein coupled receptor 173	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20190502	MGI			
1551591	Gpr173	G-protein coupled receptor 173	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1551592	Wnt5b	wingless-type MMTV integration site family, member 5B	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1551592	Wnt5b	wingless-type MMTV integration site family, member 5B	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285468
1551592	Wnt5b	wingless-type MMTV integration site family, member 5B	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285468
1551592	Wnt5b	wingless-type MMTV integration site family, member 5B	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285468
1551592	Wnt5b	wingless-type MMTV integration site family, member 5B	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1551592	Wnt5b	wingless-type MMTV integration site family, member 5B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19285468
1551594	Zfp654	zinc finger protein 654	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1551594	Zfp654	zinc finger protein 654	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1551594	Zfp654	zinc finger protein 654	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551598	Dstyk	dual serine/threonine and tyrosine protein kinase	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20180329	MGI			PMID:25400726
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10026148
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10026148
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20160526	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0004328	decreased vestibular hair cell number		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0004697	abnormal thyroid follicular cell morphology		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20160526	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0005546	choroidal neovascularization		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10026148
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20231207	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:10026148
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20160512	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10026148
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20160526	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0012671	retina spots		IAGP		N	RGD:5509061	20160526	MGI			PMID:27090238
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551601	Ap1g1	adaptor protein complex AP-1, gamma 1 subunit	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:27090238
1551602	Pard6a	par-6 family cell polarity regulator alpha	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20200402	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23636699
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20241121	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10555141
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:15215868
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:23636699
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15215868
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10555141
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20220519	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581773
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20220519	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20220519	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10555141
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0004375	enlarged frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0004379	wide frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0004386	enlarged interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:10555141
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182866
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439742
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10555141
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15215868
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10555141
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16501171
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23636699
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20241121	MGI			
1551604	Dnmt3b	DNA methyltransferase 3B	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20141003	MGI			PMID:23636699
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151203	MGI			PMID:26048142
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201022	MGI			
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20151203	MGI			PMID:26048142
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0004064	decreased susceptibility to induced muscular atrophy		IAGP		N	RGD:5509061	20151203	MGI			PMID:26048142
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20181227	MGI			
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20151203	MGI			PMID:26048142
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20151203	MGI			PMID:26048142
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20151203	MGI			PMID:26048142
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0010052	increased grip strength		IAGP		N	RGD:5509061	20151203	MGI			PMID:26048142
1551608	Usp19	ubiquitin specific peptidase 19	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551612	Nudcd2	NudC domain containing 2	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20230601	MGI			
1551612	Nudcd2	NudC domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1551612	Nudcd2	NudC domain containing 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1551615	Cct5	chaperonin containing TCP1 subunit 5	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20220519	MGI			
1551615	Cct5	chaperonin containing TCP1 subunit 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1551615	Cct5	chaperonin containing TCP1 subunit 5	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200402	MGI			
1551615	Cct5	chaperonin containing TCP1 subunit 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1551615	Cct5	chaperonin containing TCP1 subunit 5	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20221215	MGI			
1551615	Cct5	chaperonin containing TCP1 subunit 5	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1551615	Cct5	chaperonin containing TCP1 subunit 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1551615	Cct5	chaperonin containing TCP1 subunit 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551615	Cct5	chaperonin containing TCP1 subunit 5	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20241121	MGI			
1551616	Hdac5	histone deacetylase 5	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367668
1551616	Hdac5	histone deacetylase 5	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367668
1551616	Hdac5	histone deacetylase 5	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16678093
1551616	Hdac5	histone deacetylase 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367668
1551616	Hdac5	histone deacetylase 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367668
1551616	Hdac5	histone deacetylase 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367668
1551616	Hdac5	histone deacetylase 5	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20181743
1551616	Hdac5	histone deacetylase 5	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17786239
1551616	Hdac5	histone deacetylase 5	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367668
1551616	Hdac5	histone deacetylase 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367668
1551616	Hdac5	histone deacetylase 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20181743
1551616	Hdac5	histone deacetylase 5	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367668
1551619	Rph3al	rabphilin 3A-like (without C2 domains)	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15159548
1551619	Rph3al	rabphilin 3A-like (without C2 domains)	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15159548
1551619	Rph3al	rabphilin 3A-like (without C2 domains)	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15159548
1551619	Rph3al	rabphilin 3A-like (without C2 domains)	gene	MP:0009161	pancreatic acinar cell zymogen granule accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15159548
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0008167	increased B-1a cell number		IEA		N	RGD:5509061	20241121	MGI			
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0011229	abnormal vitamin C level		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0011230	abnormal folic acid level		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0012604	decreased glutathione level		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0013890	increased CD8-positive, CD25-positive alpha-beta T cell number		IEA		N	RGD:5509061	20241121	MGI			
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0014174	decreased fatty acid beta-oxidation		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0030623	decreased cysteine level		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551620	Aldh1l2	aldehyde dehydrogenase 1 family, member L2	gene	MP:0030685	decreased cystathionine level		IAGP		N	RGD:5509061	20210204	MGI			PMID:33168096
1551622	Btla	B and T lymphocyte associated	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12796776
1551622	Btla	B and T lymphocyte associated	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128774
1551622	Btla	B and T lymphocyte associated	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1551622	Btla	B and T lymphocyte associated	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19342624
1551622	Btla	B and T lymphocyte associated	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1551622	Btla	B and T lymphocyte associated	gene	MP:0004752	decreased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1551622	Btla	B and T lymphocyte associated	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12796776
1551622	Btla	B and T lymphocyte associated	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1551622	Btla	B and T lymphocyte associated	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12796776
1551622	Btla	B and T lymphocyte associated	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12796776
1551622	Btla	B and T lymphocyte associated	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1551622	Btla	B and T lymphocyte associated	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12796776
1551622	Btla	B and T lymphocyte associated	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12796776
1551622	Btla	B and T lymphocyte associated	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12796776
1551622	Btla	B and T lymphocyte associated	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1551622	Btla	B and T lymphocyte associated	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237069
1551622	Btla	B and T lymphocyte associated	gene	MP:0008749	abnormal peripheral T cell anergy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19342624
1551626	Dad1	defender against cell death 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10336695
1551626	Dad1	defender against cell death 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748466
1551626	Dad1	defender against cell death 1	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10336695
1551626	Dad1	defender against cell death 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10336695
1551626	Dad1	defender against cell death 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748466
1551626	Dad1	defender against cell death 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10336695
1551626	Dad1	defender against cell death 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748466
1551626	Dad1	defender against cell death 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10336695
1551626	Dad1	defender against cell death 1	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0011187	abnormal parietal endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0011197	abnormal proamniotic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0011200	abnormal extraembryonic coelom morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0012095	increased Reichert's membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0012299	hydropic allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:10720432
1551626	Dad1	defender against cell death 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:10748466
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10197978
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585856
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640975
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10197978
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874264
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10197978
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20111116	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001182	lung hemorrhage		IEA		N	RGD:5509061	20141003	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831701
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17585010
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640975
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001861	lung inflammation		IEA		N	RGD:5509061	20141003	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002023	increased B cell derived lymphoma incidence		IEA		N	RGD:5509061	20141003	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10197978
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002144	abnormal B cell differentiation		IEA		N	RGD:5509061	20111116	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002145	abnormal T cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831701
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002421	abnormal cell-mediated immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10606629
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10197978
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585856
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312133
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10606629
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002445	abnormal mononuclear cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585856
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002463	abnormal neutrophil physiology		IEA		N	RGD:5509061	20111116	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002465	abnormal eosinophil physiology		IEA		N	RGD:5509061	20111116	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17347685
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640975
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0002619	abnormal lymphocyte morphology		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640975
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15944314
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10606629
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831701
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004944	abnormal B cell negative selection		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10197978
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17585010
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005068	abnormal NK cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11896280
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IEA		N	RGD:5509061	20111116	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17585010
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IEA		N	RGD:5509061	20111116	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005150	cachexia		IEA		N	RGD:5509061	20111116	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10606629
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:17347685
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005673	decreased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20141003	MGI			PMID:11896280
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005673	decreased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585856
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0005673	decreased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312133
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17347685
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11896280
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20180215	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008112	abnormal monocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15585856
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874264
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831701
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008240	abnormal spleen marginal zone macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874264
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312133
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17585010
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008560	increased tumor necrosis factor secretion		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008564	increased interferon-beta secretion		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17585010
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831701
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21421839
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008744	abnormal B cell anergy		IAGP		N	RGD:5509061	20191128	MGI			PMID:22078222
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17585010
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640975
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736736
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640975
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10606629
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0009318	increased splenic marginal zone lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21640975
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17347685
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10606629
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620849
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161749
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956547
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20190418	MGI			
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0014471	enhanced B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:10606629
1551628	Inpp5d	inositol polyphosphate-5-phosphatase D	gene	MP:0014990	enhanced erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:21421839
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20150730	MGI			PMID:8830097
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20180215	MGI			PMID:8830097
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20180215	MGI			PMID:8830097
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20150730	MGI			PMID:8830097
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20150730	MGI			PMID:8830097
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20150730	MGI			PMID:8830097
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150730	MGI			PMID:8830097
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20150730	MGI			PMID:8830097
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20150730	MGI			PMID:8830097
1551629	4930453N24Rik	RIKEN cDNA 4930453N24 gene	gene	MP:0030542	abnormal dentin development		IAGP		N	RGD:5509061	20180215	MGI			PMID:8830097
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401273
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401273
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22634729
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:22634729
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0002284	abnormal tracheal smooth muscle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0002285	abnormal tracheal ciliated epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24476694
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:24476694
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24476694
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401273
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401273
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24476694
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401273
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401273
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401273
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24476694
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24476694
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24476694
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0010988	abnormal bronchial cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0010994	aerophagia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18585372
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401273
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0011460	decreased urine chloride ion level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24476694
1551631	Ano1	anoctamin 1, calcium activated chloride channel	gene	MP:0014208	decreased intestinal epithelial chloride transmembrane transport		IAGP		N	RGD:5509061	20200310	MGI			PMID:24974903
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16176985
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17307907
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873445
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0000664	small prostate gland anterior lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001158	abnormal prostate gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230601	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20191226	MGI			PMID:16176985
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16176985
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17307907
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16176985
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873445
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002212	abnormal secondary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17307907
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002771	absent prostate gland anterior lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002789	male pseudohermaphroditism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20241121	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20210128	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0003553	abnormal foreskin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873445
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0004930	small epididymis		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0005187	abnormal penis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0005188	small penis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0006415	absent testes		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0009198	abnormal male genitalia morphology		IEA		N	RGD:5509061	20231207	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17307907
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0009662	abnormal uterine receptivity		IAGP		N	RGD:5509061	20191226	MGI			PMID:16176985
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0009664	abnormal luminal closure		IAGP		N	RGD:5509061	20191226	MGI			PMID:16176985
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0009735	abnormal prostate gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0031286	unilateral cryptorchism		IAGP		N	RGD:5509061	20211014	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0031294	penile hypospadia		IAGP		N	RGD:5509061	20211014	MGI			PMID:17142810
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0031378	ambiguous external male genitalia		IAGP		N	RGD:5509061	20220421	MGI			PMID:15831525
1551632	Fkbp4	FK506 binding protein 4	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:16873445
1551634	Apom	apolipoprotein M	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18381283
1551634	Apom	apolipoprotein M	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1551634	Apom	apolipoprotein M	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18006500
1551634	Apom	apolipoprotein M	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1551634	Apom	apolipoprotein M	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210520	MGI			
1551634	Apom	apolipoprotein M	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18006500
1551634	Apom	apolipoprotein M	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20210520	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20201022	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0000322	increased granulocyte number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0001916	intracerebral hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0004794	increased anti-nuclear antigen antibody level		IEA		N	RGD:5509061	20201022	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20170105	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20170105	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008097	increased plasma cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008173	increased follicular B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008182	decreased marginal zone B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008206	increased B-2 B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008346	increased gamma-delta T cell number		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0009820	abnormal liver vasculature morphology		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0009926	decreased transitional stage T2 B cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20201022	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0012765	decreased alpha-beta T cell number		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0012767	increased KLRG1-positive NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013022	increased Ly6C high monocyte number		IEA		N	RGD:5509061	20170105	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013154	increased KLRG1+ CD8-positive alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013157	increased KLRG1+ CD4 alpha-beta T cell number		IEA		N	RGD:5509061	20181227	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013417	decreased memory-marker gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013418	increased memory-marker gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013421	increased CD5-positive gamma-delta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013426	decreased memory-marker NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013427	increased memory-marker NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013430	increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013433	increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013511	increased CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013513	decreased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013519	decreased CD4-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013522	decreased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013669	decreased Ly6C-positive immature NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013675	decreased Ly6C-positive mature NK cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013775	increased KLRG1-positive T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0013975	abnormal coronary sinus connection		IEA		N	RGD:5509061	20170504	MGI			
1551639	Cog6	component of oligomeric golgi complex 6	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1551641	Tsnax	translin-associated factor X	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20240523	MGI			
1551641	Tsnax	translin-associated factor X	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20240523	MGI			
1551641	Tsnax	translin-associated factor X	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20240523	MGI			
1551641	Tsnax	translin-associated factor X	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20241121	MGI			
1551641	Tsnax	translin-associated factor X	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1551641	Tsnax	translin-associated factor X	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20240523	MGI			
1551641	Tsnax	translin-associated factor X	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20211230	MGI			PMID:26096928
1551641	Tsnax	translin-associated factor X	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20211230	MGI			PMID:26096928
1551641	Tsnax	translin-associated factor X	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20241121	MGI			
1551641	Tsnax	translin-associated factor X	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20211230	MGI			PMID:26096928
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20231207	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20231207	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20241121	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20231207	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191219	MGI			PMID:27707879
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20241121	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20231207	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20201022	MGI			PMID:27430022
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20231207	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20231207	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20231207	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:27430022
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0008060	abnormal podocyte slit diaphragm morphology		IAGP		N	RGD:5509061	20201022	MGI			PMID:27430022
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20231207	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20201022	MGI			PMID:27430022
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201022	MGI			PMID:27430022
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0011430	mesangiolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551642	Kirrel1	kirre like nephrin family adhesion molecule 1	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416156
1551651	Morc2a	microrchidia 2A	gene	MP:0000026	abnormal inner ear morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000049	abnormal middle ear morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000075	absent neurocranium		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000104	abnormal sphenoid bone morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000141	abnormal vertebral body morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000149	abnormal scapula morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000297	abnormal atrioventricular cushion morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0000454	abnormal jaw morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000550	abnormal forelimb morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000552	abnormal radius morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000553	absent radius		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000554	abnormal carpal bone morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000565	oligodactyly		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000613	abnormal salivary gland morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000614	absent salivary gland		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000632	abnormal pineal gland morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000633	abnormal pituitary gland morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000705	athymia		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000819	abnormal olfactory bulb morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000820	abnormal choroid plexus morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0000899	abnormal corpora quadrigemina morphology		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0001014	absent superior cervical ganglion		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0001067	absent mandibular nerve		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0001093	small trigeminal ganglion		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0001127	small ovary		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0001916	intracerebral hemorrhage		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0002237	abnormal nasal cavity morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0002239	abnormal nasal septum morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0002243	abnormal vomeronasal organ morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0002279	abnormal diaphragm morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0002951	small thyroid gland		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0003078	aphakia		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0003327	liver cyst		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0003924	diaphragmatic hernia		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004234	abnormal masticatory muscle morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004247	small pancreas		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004352	absent humerus		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004440	absent occipital bone		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004666	absent stapedial artery		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004668	absent vertebral body		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004790	absent upper incisors		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0005105	abnormal middle ear ossicle morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005107	abnormal stapes morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005108	abnormal ulna morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005113	decreased spinal cord ventral horn cell number		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0005157	holoprosencephaly		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0005236	abnormal olfactory nerve morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0005269	abnormal occipital bone morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005298	abnormal clavicle morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005315	absent pituitary gland		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005358	abnormal incisor morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0005587	abnormal Meckel's cartilage morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0006033	abnormal external auditory canal morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0006425	absent Mullerian ducts		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0008128	abnormal brain internal capsule morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0008878	abnormal DNA methylation during gametogenesis		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0009073	absent Wolffian ducts		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0009495	abnormal common bile duct morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0009569	abnormal left lung morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0009570	abnormal right lung morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0009707	absent external auditory canal		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0009771	absent optic chiasm		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0009820	abnormal liver vasculature morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0009904	tongue hypoplasia		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0009917	abnormal hyoid bone body morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0010434	double inlet heart right ventricle		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0010465	aberrant origin of the right subclavian artery		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0010496	abnormal pectinate muscle morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0011380	enlarged brain ventricles		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0012091	increased midbrain size		IAGP		N	RGD:5509061	20230126	MGI			PMID:36332029
1551651	Morc2a	microrchidia 2A	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20260402	MGI			PMID:41414675
1551651	Morc2a	microrchidia 2A	gene	MP:0013816	absent digastric muscle		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013822	abnormal anterior cerebral artery morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013823	absent segment of anterior cerebral artery		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013830	abnormal intrathoracic topology of vagus nerve		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013851	abnormal Wolffian duct topology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013854	abnormal celiac artery morphology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013865	abnormal dorsal pancreas topology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013874	abnormal ductus venosus topology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013875	increased trigeminal neuroma incidence		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013914	absent intracranial segment of vertebral artery		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013927	abnormal facial nerve topology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013929	absent eye muscles		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013931	abnormal olfactory bulb position		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013932	fragmented Meckel's cartilage		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013936	abnormal thymus topology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013943	abnormal ureter topology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013952	retroesophageal left subclavian artery		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013953	left sided brachiocephalic trunk		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013979	abnormal subclavian artery origin		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013987	absent intrahepatic inferior vena cava segment		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013992	persistent dorsal ophthalmic artery		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013996	abnormal vertebral artery origin		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0013997	abnormal internal carotid artery topology		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0014006	absent posterior communicating artery		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0014023	abnormal intestine placement		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0014110	absent ventral pancreas		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0014111	small ventral pancreas		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0014113	small dorsal pancreas		IEA		N	RGD:5509061	20200310	MGI			
1551651	Morc2a	microrchidia 2A	gene	MP:0014114	abnormal cognition		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20240215	MGI			PMID:34695197
1551651	Morc2a	microrchidia 2A	gene	MP:0020301	short tongue		IEA		N	RGD:5509061	20200310	MGI			
1551652	Nfya	nuclear transcription factor-Y alpha	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14678971
1551652	Nfya	nuclear transcription factor-Y alpha	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14678971
1551652	Nfya	nuclear transcription factor-Y alpha	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20150212	MGI			PMID:14678971
1551652	Nfya	nuclear transcription factor-Y alpha	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:14678971
1551654	Pou6f2	POU domain, class 6, transcription factor 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20200310	MGI			
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11051546
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000119	abnormal tooth eruption		IAGP		N	RGD:5509061	20160825	MGI			PMID:24127173
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11051546
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26659571
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085748
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160825	MGI			PMID:24127173
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002351	abnormal cervical lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085748
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085748
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20161013	MGI			PMID:26659571
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004983	abnormal osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085748
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11051546
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20160825	MGI			PMID:24127173
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008119	decreased Langerhans cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606662
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008162	increased diameter of tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008233	abnormal pro-B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008464	absent peripheral lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085748
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008464	absent peripheral lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085748
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085748
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0009633	absent cervical lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11085748
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0009917	abnormal hyoid bone body morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11051546
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22068587
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21909105
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0011999	abnormal tail length		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0013614	abnormal areal bone mineral density		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0013617	increased areal bone mineral density		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0013619	abnormal long bone internal diameter		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0013619	abnormal long bone internal diameter		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0013621	decreased internal diameter of femur		IAGP		N	RGD:5509061	20151112	MGI			PMID:26234751
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20220922	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:10984520
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0020080	increased bone mineralization		IAGP		N	RGD:5509061	20160818	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0021183	increased femoral compact bone area		IAGP		N	RGD:5509061	20241121	MGI			PMID:19016581
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0021187	increased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:21909103
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0030072	round face		IAGP		N	RGD:5509061	20170921	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0030279	thin neurocranium		IAGP		N	RGD:5509061	20171102	MGI			PMID:9950424
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0030469	optic canal stenosis		IAGP		N	RGD:5509061	20171221	MGI			PMID:22836362
1551655	Tnfsf11	tumor necrosis factor (ligand) superfamily, member 11	gene	MP:0031278	decreased osteosarcoma incidence		IAGP		N	RGD:5509061	20210805	MGI			PMID:26659571
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0003174	increased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8262065
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8262065
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11105922
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8262065
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8262065
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8806828
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8262064
1551656	M6pr	mannose-6-phosphate receptor, cation dependent	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24355925
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18345009
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22123939
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0001619	abnormal vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:18345009
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24355925
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:18345009
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0003711	pathological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18345009
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24355925
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20201015	MGI			PMID:30825241
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20201015	MGI			PMID:30825241
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20201015	MGI			PMID:30825241
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20201015	MGI			PMID:30825241
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24355925
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20201015	MGI			PMID:30825241
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210422	MGI			
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0011132	abnormal lung endothelial cell migration		IAGP		N	RGD:5509061	20211125	MGI			PMID:18345009
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0012107	enhanced exercise endurance		IAGP		N	RGD:5509061	20201015	MGI			PMID:30825241
1551657	Robo4	roundabout guidance receptor 4	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20201015	MGI			PMID:30825241
1551659	Esam	endothelial cell-specific adhesion molecule	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819200
1551659	Esam	endothelial cell-specific adhesion molecule	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818677
1551659	Esam	endothelial cell-specific adhesion molecule	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819200
1551659	Esam	endothelial cell-specific adhesion molecule	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818677
1551659	Esam	endothelial cell-specific adhesion molecule	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818677
1551659	Esam	endothelial cell-specific adhesion molecule	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12819200
1551659	Esam	endothelial cell-specific adhesion molecule	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818677
1551664	Iqcg	IQ motif containing G	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855593
1551664	Iqcg	IQ motif containing G	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855593
1551664	Iqcg	IQ motif containing G	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551664	Iqcg	IQ motif containing G	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24362311
1551664	Iqcg	IQ motif containing G	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551664	Iqcg	IQ motif containing G	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551664	Iqcg	IQ motif containing G	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551664	Iqcg	IQ motif containing G	gene	MP:0002675	asthenozoospermia		IEA		N	RGD:5509061	20200310	MGI			
1551664	Iqcg	IQ motif containing G	gene	MP:0002687	oligozoospermia		IEA		N	RGD:5509061	20200310	MGI			
1551664	Iqcg	IQ motif containing G	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855593
1551664	Iqcg	IQ motif containing G	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24362311
1551664	Iqcg	IQ motif containing G	gene	MP:0005578	teratozoospermia		IEA		N	RGD:5509061	20200310	MGI			
1551664	Iqcg	IQ motif containing G	gene	MP:0008545	absent sperm flagellum		IEA		N	RGD:5509061	20200310	MGI			
1551664	Iqcg	IQ motif containing G	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551664	Iqcg	IQ motif containing G	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551664	Iqcg	IQ motif containing G	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551664	Iqcg	IQ motif containing G	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551664	Iqcg	IQ motif containing G	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551664	Iqcg	IQ motif containing G	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220324	MGI			PMID:24849454
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20170105	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20230824	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001759	increased urine glucose level		IEA		N	RGD:5509061	20211021	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0002959	increased urine microalbumin level		IEA		N	RGD:5509061	20211021	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20201022	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0011085	postnatal lethality, complete penetrance		IEA		N	RGD:5509061	20230824	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0011128	increased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0030973	impaired gluconeogenesis		IAGP		N	RGD:5509061	20200116	MGI			PMID:28973305
1551668	Agpat1	1-acylglycerol-3-phosphate O-acyltransferase 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:28973305
1551670	Arhgap26	Rho GTPase activating protein 26	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1551670	Arhgap26	Rho GTPase activating protein 26	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20221215	MGI			
1551670	Arhgap26	Rho GTPase activating protein 26	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20150910	MGI			PMID:25019370
1551670	Arhgap26	Rho GTPase activating protein 26	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20211125	MGI			PMID:25019370
1551670	Arhgap26	Rho GTPase activating protein 26	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:25019370
1551670	Arhgap26	Rho GTPase activating protein 26	gene	MP:0030959	abnormal myoblast fusion		IAGP		N	RGD:5509061	20211125	MGI			PMID:25019370
1551679	Pla2g2f	phospholipase A2, group IIF	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20260402	MGI			
1551679	Pla2g2f	phospholipase A2, group IIF	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1551679	Pla2g2f	phospholipase A2, group IIF	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1551679	Pla2g2f	phospholipase A2, group IIF	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1551679	Pla2g2f	phospholipase A2, group IIF	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1551679	Pla2g2f	phospholipase A2, group IIF	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20230119	MGI			
1551679	Pla2g2f	phospholipase A2, group IIF	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230119	MGI			
1551679	Pla2g2f	phospholipase A2, group IIF	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1551679	Pla2g2f	phospholipase A2, group IIF	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230119	MGI			
1551682	Ephb1	Eph receptor B1	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20201022	MGI			
1551682	Ephb1	Eph receptor B1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1551682	Ephb1	Eph receptor B1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1551682	Ephb1	Eph receptor B1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1551682	Ephb1	Eph receptor B1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143520
1551682	Ephb1	Eph receptor B1	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1551682	Ephb1	Eph receptor B1	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12971893
1551682	Ephb1	Eph receptor B1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1551682	Ephb1	Eph receptor B1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12971893
1551682	Ephb1	Eph receptor B1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1551682	Ephb1	Eph receptor B1	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:30185604
1551682	Ephb1	Eph receptor B1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1551682	Ephb1	Eph receptor B1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20201022	MGI			
1551682	Ephb1	Eph receptor B1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:23143520
1551682	Ephb1	Eph receptor B1	gene	MP:0004267	abnormal optic tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12971893
1551682	Ephb1	Eph receptor B1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182796
1551682	Ephb1	Eph receptor B1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21847105
1551682	Ephb1	Eph receptor B1	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1551682	Ephb1	Eph receptor B1	gene	MP:0008228	increased anterior commissure size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1551682	Ephb1	Eph receptor B1	gene	MP:0008960	abnormal axon pruning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182796
1551682	Ephb1	Eph receptor B1	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1551682	Ephb1	Eph receptor B1	gene	MP:0012462	decreased brain internal capsule size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1551682	Ephb1	Eph receptor B1	gene	MP:0012484	decreased corticospinal tract size		IAGP		N	RGD:5509061	20160526	MGI			PMID:24997765
1551682	Ephb1	Eph receptor B1	gene	MP:0014746	abnormal hippocampal mossy fiber innervation pattern		IAGP		N	RGD:5509061	20250911	MGI			PMID:30185604
1551682	Ephb1	Eph receptor B1	gene	MP:0020140	increased brain external capsule size		IAGP		N	RGD:5509061	20160616	MGI			PMID:24997765
1551683	Herc4	hect domain and RLD 4	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967448
1551683	Herc4	hect domain and RLD 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967448
1551683	Herc4	hect domain and RLD 4	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551683	Herc4	hect domain and RLD 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967448
1551683	Herc4	hect domain and RLD 4	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551683	Herc4	hect domain and RLD 4	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17967448
1551685	Nme3	NME/NM23 nucleoside diphosphate kinase 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20251211	MGI			PMID:38480688
1551685	Nme3	NME/NM23 nucleoside diphosphate kinase 3	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20251211	MGI			PMID:38480688
1551685	Nme3	NME/NM23 nucleoside diphosphate kinase 3	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22438820
1551685	Nme3	NME/NM23 nucleoside diphosphate kinase 3	gene	MP:0031252	abnormal physiological response to hypoxia		IAGP		N	RGD:5509061	20251211	MGI			PMID:38480688
1551686	Tsc22d2	TSC22 domain family, member 2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1551686	Tsc22d2	TSC22 domain family, member 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1551686	Tsc22d2	TSC22 domain family, member 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20250508	MGI			
1551686	Tsc22d2	TSC22 domain family, member 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20260402	MGI			
1551686	Tsc22d2	TSC22 domain family, member 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1551686	Tsc22d2	TSC22 domain family, member 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1551686	Tsc22d2	TSC22 domain family, member 2	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20260402	MGI			
1551686	Tsc22d2	TSC22 domain family, member 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176562
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:22464323
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176562
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176562
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18176562
1551687	Egln2	egl-9 family hypoxia-inducible factor 2	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056838
1551688	Usp45	ubiquitin specific petidase 45	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1551688	Usp45	ubiquitin specific petidase 45	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20220901	MGI			PMID:30573563
1551688	Usp45	ubiquitin specific petidase 45	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20220901	MGI			PMID:30573563
1551688	Usp45	ubiquitin specific petidase 45	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20220901	MGI			PMID:30573563
1551689	Nenf	neuron derived neurotrophic factor	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24058337
1551689	Nenf	neuron derived neurotrophic factor	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24058337
1551689	Nenf	neuron derived neurotrophic factor	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24058337
1551689	Nenf	neuron derived neurotrophic factor	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:24058337
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20200310	MGI			
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20220106	MGI			PMID:29809150
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20200310	MGI			
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20220106	MGI			PMID:29809150
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0004575	small limb buds		IAGP		N	RGD:5509061	20220106	MGI			PMID:29809150
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20200310	MGI			
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20200310	MGI			
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20220106	MGI			PMID:29809150
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220106	MGI			PMID:29809150
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20220106	MGI			PMID:29809150
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0011264	abnormal cardiac mesenchyme morphology		IAGP		N	RGD:5509061	20220106	MGI			PMID:29809150
1551690	Fbxl19	F-box and leucine-rich repeat protein 19	gene	MP:0012177	delayed head development		IAGP		N	RGD:5509061	20220106	MGI			PMID:29809150
1551691	Corin	corin, serine peptidase	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15637153
1551691	Corin	corin, serine peptidase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:18057101
1551691	Corin	corin, serine peptidase	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18057101
1551691	Corin	corin, serine peptidase	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18057101
1551691	Corin	corin, serine peptidase	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0000405	abnormal auchene hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0000423	delayed hair regrowth		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15637153
1551691	Corin	corin, serine peptidase	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15637153
1551691	Corin	corin, serine peptidase	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15637153
1551691	Corin	corin, serine peptidase	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15637153
1551691	Corin	corin, serine peptidase	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15637153
1551691	Corin	corin, serine peptidase	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15637153
1551691	Corin	corin, serine peptidase	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0008860	abnormal hair cycle telogen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0009272	decreased guard hair length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0011194	abnormal hair follicle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551691	Corin	corin, serine peptidase	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20412777
1551694	Dnajc16	DnaJ heat shock protein family (Hsp40) member C16	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1551694	Dnajc16	DnaJ heat shock protein family (Hsp40) member C16	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20160811	MGI			
1551694	Dnajc16	DnaJ heat shock protein family (Hsp40) member C16	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20180531	MGI			PMID:28900426
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20180531	MGI			PMID:28900426
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0008251	abnormal phagocyte morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20180531	MGI			PMID:28900426
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20180531	MGI			PMID:28900426
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0011890	increased circulating ferritin level		IAGP		N	RGD:5509061	20180927	MGI			PMID:29295842
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0012768	decreased KLRG1-positive NK cell number		IAGP		N	RGD:5509061	20180531	MGI			PMID:28900426
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0013667	increased immature NK cell number		IAGP		N	RGD:5509061	20180531	MGI			PMID:28900426
1551696	Il18bp	interleukin 18 binding protein	gene	MP:0013672	decreased mature NK cell number		IAGP		N	RGD:5509061	20180531	MGI			PMID:28900426
1551699	Bcl2l2	BCL2-like 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500547
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420255
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420255
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20150402	MGI			PMID:9770502
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500547
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500547
1551699	Bcl2l2	BCL2-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20150402	MGI			PMID:9770502
1551699	Bcl2l2	BCL2-like 2	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9770502
1551699	Bcl2l2	BCL2-like 2	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420255
1551699	Bcl2l2	BCL2-like 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500547
1551699	Bcl2l2	BCL2-like 2	gene	MP:0002785	absent Leydig cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420255
1551699	Bcl2l2	BCL2-like 2	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420255
1551699	Bcl2l2	BCL2-like 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500547
1551699	Bcl2l2	BCL2-like 2	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420255
1551699	Bcl2l2	BCL2-like 2	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500547
1551699	Bcl2l2	BCL2-like 2	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20150402	MGI			PMID:9770502
1551699	Bcl2l2	BCL2-like 2	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11420255
1551699	Bcl2l2	BCL2-like 2	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20150402	MGI			PMID:9770502
1551699	Bcl2l2	BCL2-like 2	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:9770502
1551699	Bcl2l2	BCL2-like 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:9770502
1551699	Bcl2l2	BCL2-like 2	gene	MP:0014331	abnormal Purkinje cell mitochondrial morphology		IAGP		N	RGD:5509061	20240718	MGI			PMID:18551174
1551699	Bcl2l2	BCL2-like 2	gene	MP:0020355	abnormal Sertoli cell barrier morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:11420255
1551699	Bcl2l2	BCL2-like 2	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220623	MGI			PMID:9770502
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20201022	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20220519	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210520	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20201022	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201022	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1551706	Phf20l1	PHD finger protein 20-like 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20201022	MGI			
1551707	Ptpre	protein tyrosine phosphatase receptor type E	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921884
1551707	Ptpre	protein tyrosine phosphatase receptor type E	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528021
1551707	Ptpre	protein tyrosine phosphatase receptor type E	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921884
1551707	Ptpre	protein tyrosine phosphatase receptor type E	gene	MP:0004357	long tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528021
1551707	Ptpre	protein tyrosine phosphatase receptor type E	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528021
1551707	Ptpre	protein tyrosine phosphatase receptor type E	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528021
1551707	Ptpre	protein tyrosine phosphatase receptor type E	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:14528021
1551707	Ptpre	protein tyrosine phosphatase receptor type E	gene	MP:0031073	decreased circulating type I collagen C-terminal telopeptide level		IAGP		N	RGD:5509061	20200618	MGI			PMID:14528021
1551707	Ptpre	protein tyrosine phosphatase receptor type E	gene	MP:0031723	abnormal podosome assembly		IAGP		N	RGD:5509061	20260507	MGI			PMID:14528021
1551708	Abtb2	ankyrin repeat and BTB domain containing 2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20150430	MGI			
1551708	Abtb2	ankyrin repeat and BTB domain containing 2	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20200402	MGI			PMID:19393728
1551708	Abtb2	ankyrin repeat and BTB domain containing 2	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20200402	MGI			PMID:25568138
1551708	Abtb2	ankyrin repeat and BTB domain containing 2	gene	MP:0020148	abnormal susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200402	MGI			PMID:19393728
1551708	Abtb2	ankyrin repeat and BTB domain containing 2	gene	MP:0020148	abnormal susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200402	MGI			PMID:25568138
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11640934
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12805218
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925882
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9603515
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20221103	MGI			
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11640934
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384379
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925882
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9603515
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001746	abnormal pituitary secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9603515
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384379
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030618
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12805218
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0002798	abnormal active avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384379
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0002802	abnormal discrimination learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11640934
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384379
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0002969	impaired social transmission of food preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:11640934
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:15029245
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925882
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:9603515
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740578
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12805218
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11753386
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:12740578
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314537
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030618
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20221103	MGI			
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9603515
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9603515
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12805218
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030618
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12805218
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384379
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314537
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:12805218
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384379
1551710	Rasgrf1	RAS protein-specific guanine nucleotide-releasing factor 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12805218
1551711	Or6b9	olfactory receptor family 6 subfamily B member 9	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186781
1551711	Or6b9	olfactory receptor family 6 subfamily B member 9	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186781
1551712	Tspan12	tetraspanin 12	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19837033
1551712	Tspan12	tetraspanin 12	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1551712	Tspan12	tetraspanin 12	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20200310	MGI			PMID:19837033
1551712	Tspan12	tetraspanin 12	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1551712	Tspan12	tetraspanin 12	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1551712	Tspan12	tetraspanin 12	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20260402	MGI			
1551712	Tspan12	tetraspanin 12	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19837033
1551712	Tspan12	tetraspanin 12	gene	MP:0004368	abnormal stria vascularis vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19837033
1551712	Tspan12	tetraspanin 12	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
1551712	Tspan12	tetraspanin 12	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1551712	Tspan12	tetraspanin 12	gene	MP:0006185	retina hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:19837033
1551712	Tspan12	tetraspanin 12	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19837033
1551712	Tspan12	tetraspanin 12	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:19837033
1551712	Tspan12	tetraspanin 12	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19837033
1551712	Tspan12	tetraspanin 12	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
1551712	Tspan12	tetraspanin 12	gene	MP:0010452	retina microaneurysm		IAGP		N	RGD:5509061	20200310	MGI			PMID:19837033
1551712	Tspan12	tetraspanin 12	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20260402	MGI			
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0000263	absent organized vascular network		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19910638
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:8846781
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19910638
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:8846781
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003288	intestinal edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003542	abnormal vascular endothelial cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0004106	lymphatic vessel hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19910638
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8846781
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223757
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1551713	Tie1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0008515	thin retina outer nuclear layer		IEA		N	RGD:5509061	20180215	MGI			
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0010235	abnormal retina inner limiting membrane morphology		IEA		N	RGD:5509061	20180215	MGI			
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IEA		N	RGD:5509061	20180215	MGI			
1551714	Impdh1	inosine monophosphate dehydrogenase 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20180215	MGI			
1551715	Foxd1	forkhead box D1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20150625	MGI			PMID:24732380
1551715	Foxd1	forkhead box D1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0002768	small adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0002990	short ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0003605	fused kidneys		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200206	MGI			PMID:30830875
1551715	Foxd1	forkhead box D1	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20200206	MGI			PMID:30830875
1551715	Foxd1	forkhead box D1	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0010987	abnormal nephrogenic mesenchyme morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551715	Foxd1	forkhead box D1	gene	MP:0011361	pelvic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666231
1551716	Fxn	frataxin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10767347
1551716	Fxn	frataxin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:10767347
1551716	Fxn	frataxin	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25104852
1551716	Fxn	frataxin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11852098
1551716	Fxn	frataxin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10767347
1551716	Fxn	frataxin	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0002883	chromatolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0002899	fatigue		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20240523	MGI			PMID:32586831
1551716	Fxn	frataxin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11852098
1551716	Fxn	frataxin	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20200310	MGI			
1551716	Fxn	frataxin	gene	MP:0005330	cardiomyopathy		IEA		N	RGD:5509061	20200310	MGI			
1551716	Fxn	frataxin	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20200310	MGI			
1551716	Fxn	frataxin	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20240523	MGI			PMID:32586831
1551716	Fxn	frataxin	gene	MP:0006038	increased mitochondrial fission		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0006404	abnormal lumbar dorsal root ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20240523	MGI			PMID:32586831
1551716	Fxn	frataxin	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20240523	MGI			PMID:32586831
1551716	Fxn	frataxin	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10767347
1551716	Fxn	frataxin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551716	Fxn	frataxin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240523	MGI			PMID:32586831
1551716	Fxn	frataxin	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20240523	MGI			PMID:32586831
1551716	Fxn	frataxin	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20240523	MGI			PMID:32586831
1551716	Fxn	frataxin	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0011638	abnormal mitochondrial chromosome morphology		IAGP		N	RGD:5509061	20240523	MGI			PMID:32586831
1551716	Fxn	frataxin	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20240523	MGI			PMID:32586831
1551716	Fxn	frataxin	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10767347
1551716	Fxn	frataxin	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551716	Fxn	frataxin	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10767347
1551716	Fxn	frataxin	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0014775	decreased skeletal muscle enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0014906	abnormal muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0014906	abnormal muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0020367	increased heart iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0020367	increased heart iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11852098
1551716	Fxn	frataxin	gene	MP:0020367	increased heart iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15028670
1551716	Fxn	frataxin	gene	MP:0020367	increased heart iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16919418
1551716	Fxn	frataxin	gene	MP:0020423	abnormal mitochondrial biogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28444186
1551716	Fxn	frataxin	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:11175786
1551716	Fxn	frataxin	gene	MP:0021161	increased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:15028670
1551718	Tomm70a	translocase of outer mitochondrial membrane 70A	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20240919	MGI			
1551718	Tomm70a	translocase of outer mitochondrial membrane 70A	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20240919	MGI			
1551718	Tomm70a	translocase of outer mitochondrial membrane 70A	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20240919	MGI			
1551718	Tomm70a	translocase of outer mitochondrial membrane 70A	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20240919	MGI			
1551718	Tomm70a	translocase of outer mitochondrial membrane 70A	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1551718	Tomm70a	translocase of outer mitochondrial membrane 70A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551718	Tomm70a	translocase of outer mitochondrial membrane 70A	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20240919	MGI			
1551718	Tomm70a	translocase of outer mitochondrial membrane 70A	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1551718	Tomm70a	translocase of outer mitochondrial membrane 70A	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1551721	Tmem45a	transmembrane protein 45a	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1551721	Tmem45a	transmembrane protein 45a	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1551721	Tmem45a	transmembrane protein 45a	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20201022	MGI			
1551721	Tmem45a	transmembrane protein 45a	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1551721	Tmem45a	transmembrane protein 45a	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1551721	Tmem45a	transmembrane protein 45a	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0000411	shiny fur		IAGP		N	RGD:5509061	20141003	MGI			PMID:6863898
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14757819
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6863898
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6863898
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:6863898
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20200514	MGI			
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6863898
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0003686	abnormal eye muscle morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0008841	ruptured lens capsule		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239381
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20191226	MGI			PMID:3955134
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0031345	developmental cataract		IAGP		N	RGD:5509061	20220217	MGI			PMID:6863898
1551722	Tbc1d20	TBC1 domain family, member 20	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20240229	MGI			PMID:25476608
1551723	Bola3	bolA family member 3	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551723	Bola3	bolA family member 3	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551723	Bola3	bolA family member 3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551723	Bola3	bolA family member 3	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551723	Bola3	bolA family member 3	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551723	Bola3	bolA family member 3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551723	Bola3	bolA family member 3	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551723	Bola3	bolA family member 3	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551723	Bola3	bolA family member 3	gene	MP:0014145	increased white adipose tissue mass		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551723	Bola3	bolA family member 3	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20210520	MGI			PMID:32313871
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598041
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256469
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602620
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937578
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8638109
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598041
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256469
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551884
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290790
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290790
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12646641
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598040
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8638109
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256469
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11602620
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937578
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843678
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8638109
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551884
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290790
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20141003	MGI			PMID:12646641
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20141003	MGI			PMID:15034026
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598041
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551884
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005043	defective assembly of class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290790
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12646641
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598041
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8638109
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937578
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937578
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290790
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15034026
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8598041
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8638109
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256469
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551884
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256469
1551725	H2-DMa	histocompatibility 2, class II, locus DMa	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9551884
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20240404	MGI			PMID:38243131
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240404	MGI			PMID:38243131
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20240404	MGI			PMID:38243131
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20220811	MGI			
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20240404	MGI			PMID:38243131
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20240404	MGI			PMID:38243131
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20240404	MGI			PMID:38243131
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20250410	MGI			PMID:38243131
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:38243131
1551726	Etfdh	electron transferring flavoprotein, dehydrogenase	gene	MP:0014652	increased skeletal muscle fiber mitochondrial size		IAGP		N	RGD:5509061	20250410	MGI			PMID:38243131
1551728	Zfp251	zinc finger protein 251	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20231026	MGI			PMID:36565788
1551728	Zfp251	zinc finger protein 251	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20231026	MGI			PMID:36565788
1551728	Zfp251	zinc finger protein 251	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20231026	MGI			PMID:36565788
1551728	Zfp251	zinc finger protein 251	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20231026	MGI			PMID:36565788
1551728	Zfp251	zinc finger protein 251	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20231026	MGI			PMID:36565788
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20200310	MGI			
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0003064	decreased coping response		IEA		N	RGD:5509061	20210128	MGI			
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20200310	MGI			
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0011192	decreased embryonic epiblast cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20200310	MGI			PMID:31276560
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1551730	Elof1	ELF1 homolog, elongation factor 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240620	MGI			PMID:31276560
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150416	MGI			PMID:25112520
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20150416	MGI			PMID:25112520
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0001939	secondary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0003578	absent ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0004894	uterus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0004895	vagina atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0005644	agonadal		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0005652	sex reversal		IAGP		N	RGD:5509061	20150416	MGI			PMID:25112520
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0006415	absent testes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706291
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0021092	abnormal dorsal interneuron 1 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:18701067
1551735	Lhx9	LIM homeobox protein 9	gene	MP:0030934	decreased primordial germ cell proliferation		IAGP		N	RGD:5509061	20190411	MGI			PMID:10706291
1551746	Arl10	ADP-ribosylation factor-like 10	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1551746	Arl10	ADP-ribosylation factor-like 10	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20150430	MGI			
1551746	Arl10	ADP-ribosylation factor-like 10	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000022	abnormal ear shape		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037550
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000040	decreased middle ear ossicle number		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000073	absent craniofacial bones		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000073	absent craniofacial bones		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:18501887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:23546880
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000094	absent alveolar process		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:23546880
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000099	absent vomer bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000100	abnormal ethmoid bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000103	nasal bone hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000103	nasal bone hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000103	nasal bone hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20180201	MGI			PMID:26341559
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037550
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:18483623
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:21982646
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:22745308
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:26341559
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20190822	MGI			PMID:31232685
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221020	MGI			PMID:33772547
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230629	MGI			PMID:28408410
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000128	growth retardation of molars		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20220616	MGI			PMID:28829946
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18188448
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36745292
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20180201	MGI			PMID:18501887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20180201	MGI			PMID:16557299
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:36745292
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20181122	MGI			PMID:25818501
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18483623
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22991437
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23454479
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23546880
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24497849
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20180201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:19047372
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:30842416
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000678	abnormal parathyroid gland morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20180201	MGI			PMID:17652354
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20180201	MGI			PMID:15198977
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15987955
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20614471
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20180201	MGI			PMID:20614471
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20180201	MGI			PMID:17166916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20180201	MGI			PMID:17693261
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20180201	MGI			PMID:12682014
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12682014
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21502507
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000906	abnormal trigeminal V mesencephalic nucleus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221970
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:21502507
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20180201	MGI			PMID:20220021
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20180201	MGI			PMID:20220021
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20180201	MGI			PMID:16267821
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19421194
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20180201	MGI			PMID:15198977
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20180201	MGI			PMID:19421194
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18849985
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20180201	MGI			PMID:18849985
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20180201	MGI			PMID:26418744
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0000969	abnormal nociceptor morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26418744
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18501887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001011	abnormal superior cervical ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001026	abnormal adrenergic neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17531968
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001034	abnormal parasympathetic ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20133851
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17075884
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17075884
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17075884
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001062	absent oculomotor nerve		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15198977
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20133851
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23055936
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18849985
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23055936
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20180201	MGI			PMID:23055936
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001107	decreased Schwann cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001109	absent Schwann cell precursors		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20180201	MGI			PMID:20346763
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191003	MGI			PMID:30842416
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:17693261
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20231109	MGI			PMID:36745292
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20180201	MGI			PMID:18693272
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20180201	MGI			PMID:16203745
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20180201	MGI			PMID:16207763
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20180201	MGI			PMID:16203745
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20180201	MGI			PMID:20568247
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20180201	MGI			PMID:17428831
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20180201	MGI			PMID:22503753
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001307	fused cornea and lens		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20568247
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20180201	MGI			PMID:20568247
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20180201	MGI			PMID:16203745
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20180201	MGI			PMID:16203745
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18483623
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001347	absent lacrimal glands		IAGP		N	RGD:5509061	20180201	MGI			PMID:22745308
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23134367
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20180201	MGI			PMID:23134367
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20220616	MGI			PMID:28829946
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180201	MGI			PMID:15987955
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180201	MGI			PMID:23792428
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180201	MGI			PMID:23792428
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20220616	MGI			PMID:28829946
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20180201	MGI			PMID:20346763
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:23134367
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20180201	MGI			PMID:23134367
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001490	abnormal vibrissae reflex		IAGP		N	RGD:5509061	20180201	MGI			PMID:15198977
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180201	MGI			PMID:15987955
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180201	MGI			PMID:21413144
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20180201	MGI			PMID:17693261
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20180201	MGI			PMID:17693261
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18188448
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:20045680
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180201	MGI			PMID:18501887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20180201	MGI			PMID:19605684
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20180201	MGI			PMID:20045680
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20180201	MGI			PMID:15198977
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0001993	abnormal blinking		IAGP		N	RGD:5509061	20180201	MGI			PMID:15198977
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20180201	MGI			PMID:23281395
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002050	increased pheochromocytoma incidence		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:12682014
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:20614471
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:26418744
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:18693272
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:23571217
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20231109	MGI			PMID:36745292
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18501887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20190822	MGI			PMID:31232685
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16557299
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20180201	MGI			PMID:17531968
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20614471
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21502507
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22991437
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:16703618
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:19605684
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:19855134
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:23303524
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26341559
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23591430
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002244	abnormal turbinate morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002251	abnormal nasopharynx morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:16332365
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:16557299
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21413144
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002735	abnormal chemical nociception		IAGP		N	RGD:5509061	20180201	MGI			PMID:20346763
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20220021
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20180201	MGI			PMID:24210822
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20180201	MGI			PMID:18693272
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20180201	MGI			PMID:18693272
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20180201	MGI			PMID:20498049
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20180201	MGI			PMID:20045680
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003092	decreased cornea stroma thickness		IAGP		N	RGD:5509061	20180201	MGI			PMID:16203745
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:18188448
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003154	abnormal soft palate morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:23454479
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20568247
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:20045680
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20231109	MGI			PMID:36745292
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003416	premature bone ossification		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003418	premature intramembranous bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:19047372
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003494	parathyroid hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20180201	MGI			PMID:23454479
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003677	abnormal ear lobe morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18483623
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003760	decreased palatal length		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003773	eclabion		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003792	abnormal major salivary gland morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003818	abnormal eye muscle development		IAGP		N	RGD:5509061	20180201	MGI			PMID:16203745
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003834	abnormal adrenergic chromaffin cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003840	abnormal coronal suture morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21502507
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:23134367
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20180201	MGI			PMID:26418744
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23792428
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004075	decreased Schwann cell precursor number		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004096	abnormal midbrain-hindbrain boundary development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16332365
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20180201	MGI			PMID:16557299
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20180201	MGI			PMID:16332365
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20180201	MGI			PMID:16557299
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004268	abnormal optic stalk morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16203745
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004283	absent cornea endothelium		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004318	absent incus		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004318	absent incus		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004318	absent incus		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004319	absent malleus		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004319	absent malleus		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004319	absent malleus		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20180201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20180201	MGI			PMID:19605684
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004379	wide frontal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004420	parietal bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004447	small basioccipital bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004448	abnormal presphenoid bone morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004449	absent presphenoid bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004450	presphenoid bone hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004451	short presphenoid bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004454	absent pterygoid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004455	pterygoid bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004458	absent alisphenoid bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004459	small alisphenoid bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004459	small alisphenoid bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004461	basisphenoid bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004468	small zygomatic bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004468	small zygomatic bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004469	abnormal zygomatic arch morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004472	broad nasal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004473	absent nasal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004473	absent nasal bone		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004474	enlarged nasal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004476	absent palatine bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004476	absent palatine bone		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004537	abnormal palatine bone horizontal plate morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004594	abnormal mandibular coronoid process morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16332365
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004791	absent lower incisors		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004830	short incisors		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004870	small premaxilla		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004870	small premaxilla		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004899	absent temporal bone squamous part		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004913	absent mandibular angle		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004913	absent mandibular angle		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004913	absent mandibular angle		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004913	absent mandibular angle		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004916	absent Reichert cartilage		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:23134367
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21502507
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:21610032
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005099	abnormal ciliary body morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20180201	MGI			PMID:16203745
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20190822	MGI			PMID:31232685
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005174	abnormal tail pigmentation		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005198	abnormal aqueous drainage system morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005203	abnormal trabecular meshwork morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005204	abnormal canal of Schlemm morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20568247
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005314	absent thyroid gland		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20180201	MGI			PMID:17531968
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20230629	MGI			PMID:28408410
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26418744
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005451	abnormal body composition		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005497	optic nerve cupping		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20180201	MGI			PMID:20568247
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005579	absent outer ear		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18188448
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006101	absent tegmentum		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006105	small tectum		IAGP		N	RGD:5509061	20180201	MGI			PMID:17166916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006106	absent tectum		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006111	abnormal coronary circulation		IAGP		N	RGD:5509061	20231109	MGI			PMID:36745292
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20180201	MGI			PMID:15789410
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21597012
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20180201	MGI			PMID:23408898
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006211	small orbits		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006219	optic nerve degeneration		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006230	iris stroma hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:20568247
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006326	conductive hearing impairment		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16332365
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19855134
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006408	dorsal root ganglion hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:18849985
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0006411	upturned snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008023	abnormal styloid process morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008052	abnormal serous gland morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:19047372
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008276	failure of intramembranous bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:19605684
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008302	thin adrenal cortex		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008372	small malleus		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008375	short malleus manubrium		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008375	short malleus manubrium		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008376	small malleus manubrium		IAGP		N	RGD:5509061	20180201	MGI			PMID:17523175
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008380	abnormal gonial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008380	abnormal gonial bone morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008381	absent gonial bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008385	absent basisphenoid bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008386	absent styloid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008386	absent styloid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008386	absent styloid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008467	absent proprioceptive neurons		IAGP		N	RGD:5509061	20220616	MGI			PMID:28829946
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008486	decreased muscle spindle number		IAGP		N	RGD:5509061	20180201	MGI			PMID:23792428
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180201	MGI			PMID:18693272
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20180201	MGI			PMID:19251646
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20180201	MGI			PMID:23546880
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008532	decreased chemical nociceptive threshold		IAGP		N	RGD:5509061	20180201	MGI			PMID:18849985
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008534	enlarged fourth ventricle		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:24497849
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008818	abnormal interfrontal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19047372
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008932	abnormal embryonic tissue physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22745308
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20180201	MGI			PMID:20614471
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20180201	MGI			PMID:21246653
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009025	abnormal brain dura mater morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009039	absent inferior colliculus		IAGP		N	RGD:5509061	20180201	MGI			PMID:12682014
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009048	enlarged tectum		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009284	abnormal sympathetic neuron innervation pattern		IAGP		N	RGD:5509061	20180201	MGI			PMID:22343533
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009284	abnormal sympathetic neuron innervation pattern		IAGP		N	RGD:5509061	20180201	MGI			PMID:23454479
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009379	abnormal foot pigmentation		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009386	abnormal dermal melanocyte morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:21610032
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009388	abnormal epidermal melanocyte morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:21610032
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20180201	MGI			PMID:24052814
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009483	enlarged ileum		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009654	abnormal primary palate development		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20180201	MGI			PMID:23546880
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20230302	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:20045680
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009782	abnormal basicranium angle		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:25818501
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009798	abnormal ophthalmic nerve morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24052814
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009844	abnormal neural crest cell apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18242513
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009859	eye opacity		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:23546880
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009884	palatal shelf fusion with tongue or mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037550
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20180201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23546880
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221020	MGI			PMID:33772547
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009889	persistence of medial edge epithelium during palatal shelf fusion		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:23546880
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009891	abnormal palate bone morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009892	palate bone hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009893	cleft primary palate		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009894	absent hard palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009896	palatine bone horizontal plate hypoplasia		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009896	palatine bone horizontal plate hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009897	decreased maxillary shelf size		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16221970
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20190822	MGI			PMID:31232685
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20190822	MGI			PMID:31232685
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009906	increased tongue size		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009913	abnormal hyoid bone greater horn morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009915	absent hyoid bone lesser horns		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009917	abnormal hyoid bone body morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:18501887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23591430
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21502507
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010017	visceral vascular congestion		IAGP		N	RGD:5509061	20180201	MGI			PMID:17531968
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010043	abnormal frontonasal suture morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010241	abnormal aortic arch development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010252	anterior subcapsular cataract		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010361	increased gangliosarcoma incidence		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010362	increased ganglioneuroma incidence		IAGP		N	RGD:5509061	20180201	MGI			PMID:12469121
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010395	abnormal pharyngeal arch development		IAGP		N	RGD:5509061	20180201	MGI			PMID:20596238
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:16332365
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:36745292
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:12490557
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:16557299
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010449	heart right ventricle outflow tract stenosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010457	pulmonary artery stenosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010460	pulmonary artery hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010464	abnormal aortic arch and aortic arch branch attachment		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010464	abnormal aortic arch and aortic arch branch attachment		IAGP		N	RGD:5509061	20180201	MGI			PMID:15741317
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010464	abnormal aortic arch and aortic arch branch attachment		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010472	abnormal ascending aorta and coronary artery attachment		IAGP		N	RGD:5509061	20180201	MGI			PMID:16624854
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010485	aortic arch hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:16557299
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010563	increased heart right ventricle size		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010565	absent fetal ductus arteriosus		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010583	abnormal conotruncus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010584	abnormal conotruncus septation		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010587	conotruncal ridge hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010589	common truncal valve		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010663	abnormal brachiocephalic trunk morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010706	ventral rotation of lens		IAGP		N	RGD:5509061	20180201	MGI			PMID:16207763
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010707	decreased ventral retina size		IAGP		N	RGD:5509061	20180201	MGI			PMID:16207763
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010710	absent sclera		IAGP		N	RGD:5509061	20180201	MGI			PMID:16203745
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010711	persistent hyperplastic primary vitreous		IAGP		N	RGD:5509061	20180201	MGI			PMID:16207763
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010714	iris coloboma		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0010719	ciliary body coloboma		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:16332365
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17693261
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18188448
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:21982646
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17553423
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17172441
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18849985
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19605684
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:20045680
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:22745308
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:22991437
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:23454479
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:23546880
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20181122	MGI			PMID:25818501
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19605684
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36745292
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:16557299
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:33772547
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:22991437
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:23410975
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20181227	MGI			PMID:27001213
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17531968
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18501887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18952847
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:21098571
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17183527
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011210	abnormal temporomandibular joint morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011262	abnormal pharyngeal arch mesenchyme morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011262	abnormal pharyngeal arch mesenchyme morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:19008477
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011615	submucous cleft palate		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011627	decreased skin pigmentation		IAGP		N	RGD:5509061	20181220	MGI			PMID:21610032
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:16332365
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20240118	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20180503	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012023	decreased melanocyte number		IAGP		N	RGD:5509061	20181220	MGI			PMID:21610032
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012077	webbed neck		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22156581
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20180201	MGI			PMID:20614471
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20180201	MGI			PMID:16267821
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012090	midbrain hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012091	increased midbrain size		IAGP		N	RGD:5509061	20180201	MGI			PMID:21502507
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012091	increased midbrain size		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20180201	MGI			PMID:16267821
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20180201	MGI			PMID:20614471
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20180201	MGI			PMID:20614471
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012139	increased forebrain size		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012141	absent hindbrain		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190459
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20180201	MGI			PMID:20614471
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012174	flat head		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012490	abnormal cochlear VIII nucleus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23408898
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012516	absent metencephalon		IAGP		N	RGD:5509061	20180201	MGI			PMID:11262227
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012522	abnormal stomodeum morphology		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012523	abnormal upper lip morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012747	abnormal cardiac neural crest cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012748	increased cardiac neural crest cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012749	decreased cardiac neural crest cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012749	decreased cardiac neural crest cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:15789410
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012749	decreased cardiac neural crest cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012749	decreased cardiac neural crest cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012750	absent cardiac neural crest cells		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012751	impaired cardiac neural crest cell differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012751	impaired cardiac neural crest cell differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:17344228
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:15226263
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:15789410
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:17499702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012756	impaired cranial neural crest cell differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012757	abnormal cranial neural crest cell migration		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012759	increased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012760	decreased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012761	increased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0012761	increased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013002	decreased enteric neural crest cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:19805360
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013006	abnormal enteric neural crest cell migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013006	abnormal enteric neural crest cell migration		IAGP		N	RGD:5509061	20180201	MGI			PMID:18693272
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013199	increased head mesenchyme apoptosis		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013219	abnormal substantia nigra pars compacta morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15987955
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013262	abnormal mouth floor morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19185569
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013331	abnormal lacrimal gland development		IAGP		N	RGD:5509061	20180201	MGI			PMID:22745308
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013546	cleft soft palate		IAGP		N	RGD:5509061	20220922	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20180201	MGI			PMID:20498049
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013701	abnormal mature B cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:26061883
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013743	ciliary body hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:20568247
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013744	abnormal conjunctival sac morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16207763
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20221124	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0014563	duplicated tympanic ring		IAGP		N	RGD:5509061	20241031	MGI			PMID:16221728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0020301	short tongue		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:27483349
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0020954	decreased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20231026	MGI			PMID:28572455
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021164	oral cleft		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20220721	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20221020	MGI			PMID:33772547
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20221117	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:17927973
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:32692983
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:29986157
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:33772547
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:35151207
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021216	abnormal palatal mesenchymal cell differentiation		IAGP		N	RGD:5509061	20230302	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0021217	abnormal palatal shelf bone ossification		IAGP		N	RGD:5509061	20230223	MGI			PMID:17927973
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030026	small Meckel's cartilage		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030026	small Meckel's cartilage		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030026	small Meckel's cartilage		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030033	abnormal nasal bridge morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030049	prominent forehead		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030057	absent lacrimal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030065	face hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24700590
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030065	face hypoplasia		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030069	broad face		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030072	round face		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030072	round face		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030080	small lower incisors		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030085	syngnathia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030089	short lower incisors		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030090	short upper incisors		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030102	absent orbitosphenoid bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030107	incus hypoplasia		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030111	absent temporomandibular joint		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030112	zygomatic bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030115	abnormal nasal tip morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030119	abnormal retrotympanic process morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030120	absent retrotympanic process		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20180201	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030125	small gonial bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:12514106
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030162	absent hyoid bone body		IAGP		N	RGD:5509061	20180201	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030166	increased inner canthal distance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19251646
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030166	increased inner canthal distance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030170	absent mandibular symphysis		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030170	absent mandibular symphysis		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20221110	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030190	small snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030198	nasal septum hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030198	nasal septum hypoplasia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030199	deviated nasal septum		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030200	abnormal nasal septum cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030202	nasal septum cartilage hypoplasia		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030209	abnormal extrinsic tongue muscle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030223	mandibular hyperostosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367558
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030224	abnormal soft palate muscle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24496627
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030224	abnormal soft palate muscle morphology		IAGP		N	RGD:5509061	20221006	MGI			PMID:35212626
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030245	round head		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030249	small frontonasal prominence		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030249	small frontonasal prominence		IAGP		N	RGD:5509061	20221006	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030251	broad frontonasal prominence		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030258	small mandibular condyloid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030258	small mandibular condyloid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030258	small mandibular condyloid process		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030259	mandibular condyloid process hypoplasia		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030259	mandibular condyloid process hypoplasia		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030259	mandibular condyloid process hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030261	abnormal temporal bone zygomatic process morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030261	abnormal temporal bone zygomatic process morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030262	frontal bossing		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030268	agnathia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030269	absent mandibular ramus		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030273	mandibular retrognathia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24173031
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030275	thin frontal bone		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030276	anterior cranium occultum		IAGP		N	RGD:5509061	20180201	MGI			PMID:20106874
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030280	short parietal bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030283	small mandibular coronoid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:12975342
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030283	small mandibular coronoid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030283	small mandibular coronoid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030283	small mandibular coronoid process		IAGP		N	RGD:5509061	20221006	MGI			PMID:27362800
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030285	mandibular coronoid process hypoplasia		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030285	mandibular coronoid process hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030301	abnormal maxillary frontal process morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030302	abnormal maxillary zygomatic process morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030311	abnormal mandibular fossa morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030320	abnormal temporal bone tympanic part morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030326	decreased periocular mesenchyme apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:16207763
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030342	small maxillary prominence		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030345	enlarged maxillary prominence		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030346	small mandibular prominence		IAGP		N	RGD:5509061	20200917	MGI			PMID:31733190
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:19047372
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030351	wide coronal suture		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030367	premature metopic suture closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:19047372
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030367	premature metopic suture closure		IAGP		N	RGD:5509061	20221110	MGI			PMID:26859889
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030372	enlarged Meckel's cartilage		IAGP		N	RGD:5509061	20180201	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030374	Meckel's cartilage hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:15107405
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030374	Meckel's cartilage hypoplasia		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030374	Meckel's cartilage hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030374	Meckel's cartilage hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030377	zygomatic arch hypoplasia		IAGP		N	RGD:5509061	20181108	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030379	abnormal frontal bone squamous part morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030386	facial bone hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030416	absent temporal bone zygomatic process		IAGP		N	RGD:5509061	20180201	MGI			PMID:15037318
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030420	short basicranium		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20221215	MGI			PMID:29727702
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030447	abnormal presphenoid synchondrosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030448	premature presphenoid synchondrosis closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:18652813
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030467	abnormal cranial cartilage development		IAGP		N	RGD:5509061	20221020	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030531	abnormal facial skin morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030532	abnormal periorbital skin morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14975722
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030536	abnormal diastema morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20180726	MGI			PMID:17610273
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030681	increased circulating hydroxyproline level		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20250130	MGI			PMID:25209980
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030868	absent thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:12878728
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030869	thyroid cartilage hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030874	cricoid cartilage hypoplasia		IAGP		N	RGD:5509061	20221027	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0030908	abnormal melanocyte differentiation		IAGP		N	RGD:5509061	20181220	MGI			PMID:21610032
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031101	nasal obstruction		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:19509472
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:20568247
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:23134367
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031442	enlarged cerebral aqueduct		IAGP		N	RGD:5509061	20221103	MGI			PMID:34887903
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:26395480
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221110	MGI			PMID:30413887
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031444	glossoptosis		IAGP		N	RGD:5509061	20221027	MGI			PMID:17420000
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031444	glossoptosis		IAGP		N	RGD:5509061	20221027	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031444	glossoptosis		IAGP		N	RGD:5509061	20221027	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031445	midline cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:25451153
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031449	abnormal nasal cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:19541608
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031449	abnormal nasal cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:19706403
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031449	abnormal nasal cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:22219353
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031449	abnormal nasal cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031450	nasal cartilage hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:33155500
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031454	decreased cranial neural crest cell apoptosis		IAGP		N	RGD:5509061	20221110	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031458	absent palate bones		IAGP		N	RGD:5509061	20221124	MGI			PMID:32169905
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031459	maxillary zygomatic process hypoplasia		IAGP		N	RGD:5509061	20221201	MGI			PMID:34184034
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:17376812
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:32541010
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20221201	MGI			PMID:24433583
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:23754280
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:24785830
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:31526805
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:33772547
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031517	interrupted aortic arch, type c		IAGP		N	RGD:5509061	20240118	MGI			PMID:18058916
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031554	abnormal aortic valve development		IAGP		N	RGD:5509061	20240125	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031555	abnormal pulmonary valve development		IAGP		N	RGD:5509061	20240125	MGI			PMID:26806701
1551747	H2az2	H2A.Z histone variant 2	gene	MP:0031634	decreased heart right ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:36745292
1551748	Plekhg2	pleckstrin homology and RhoGEF domain containing G2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1551748	Plekhg2	pleckstrin homology and RhoGEF domain containing G2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18273058
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870734
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16870734
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18273058
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:10580504
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101399
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101399
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571362
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0004181	abnormal carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101399
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571362
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571362
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571362
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101399
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0008407	decreased cellular sensitivity to hydrogen peroxide		IAGP		N	RGD:5509061	20141003	MGI			PMID:10580504
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0008407	decreased cellular sensitivity to hydrogen peroxide		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571362
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10580504
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571362
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0008413	decreased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10580504
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0008486	decreased muscle spindle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:18273058
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0010021	heart vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18273058
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0020319	decreased vascular endothelial cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20190704	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231221	MGI			PMID:10809671
1551749	Shc1	src homology 2 domain-containing transforming protein C1	gene	MP:0030992	atrioventricular cushion hypoplasia		IAGP		N	RGD:5509061	20231221	MGI			PMID:10809671
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227867
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400755
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0000647	abnormal sebaceous gland morphology		IAGP		N	RGD:5509061	20150108	MGI			PMID:24685692
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20150108	MGI			PMID:24685692
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20150108	MGI			PMID:24685692
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20150108	MGI			PMID:24685692
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12911759
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227867
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858605
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12911759
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12911759
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20150108	MGI			PMID:24685692
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0003879	abnormal hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047635
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490528
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004368	abnormal stria vascularis vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400755
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490528
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227867
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490528
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227867
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004410	absent endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490528
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490528
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227867
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858605
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490528
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0004999	abnormal blood-inner ear barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400755
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400755
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12911759
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20150108	MGI			PMID:24685692
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0006332	abnormal cochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858605
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490528
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0006403	abnormal cochlear endolymph ionic homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490528
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12490528
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17227867
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20858605
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20150108	MGI			PMID:24685692
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0011968	decreased threshold for auditory brainstem response		IAGP		N	RGD:5509061	20150108	MGI			PMID:24685692
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20260402	MGI			
1551751	Gjb6	gap junction protein, beta 6	gene	MP:0013378	increased sebocyte number		IAGP		N	RGD:5509061	20150108	MGI			PMID:24685692
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017147
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18322212
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12615907
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017147
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017147
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12615907
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15315966
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12615907
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12615907
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0008837	increased transforming growth factor beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11017147
1551752	Slpi	secretory leukocyte peptidase inhibitor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18322212
1551753	Sf1	splicing factor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736371
1551753	Sf1	splicing factor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736371
1551753	Sf1	splicing factor 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736371
1551753	Sf1	splicing factor 1	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17900258
1551753	Sf1	splicing factor 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17900258
1551753	Sf1	splicing factor 1	gene	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736371
1551753	Sf1	splicing factor 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17900258
1551753	Sf1	splicing factor 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20736371
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069069
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20141003	MGI			PMID:9492004
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11069069
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9492004
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551754	H2-Oa	histocompatibility 2, O region alpha locus	gene	MP:0012702	increased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551755	Lrg1	leucine-rich alpha-2-glycoprotein 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20180920	MGI			PMID:25826092
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22349513
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22349513
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22349513
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15657444
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0008156	decreased diameter of tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15657444
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22349513
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22349513
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:22349513
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0021182	decreased femoral compact bone area		IAGP		N	RGD:5509061	20220922	MGI			PMID:16876494
1551756	Klf10	Kruppel-like transcription factor 10	gene	MP:0030483	decreased osteocyte number		IAGP		N	RGD:5509061	20171221	MGI			PMID:16876494
1551758	Pygo2	pygopus 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20221103	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19487454
1551758	Pygo2	pygopus 2	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20200310	MGI			PMID:19487454
1551758	Pygo2	pygopus 2	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20221103	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20221103	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210128	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20221103	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20221103	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20221103	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:23637336
1551758	Pygo2	pygopus 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:23637336
1551758	Pygo2	pygopus 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20221103	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20221103	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23637336
1551758	Pygo2	pygopus 2	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20221103	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0004135	abnormal mammary gland embryonic development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19487454
1551758	Pygo2	pygopus 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20200310	MGI			PMID:19487454
1551758	Pygo2	pygopus 2	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19487454
1551758	Pygo2	pygopus 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23637336
1551758	Pygo2	pygopus 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0010174	decreased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19487454
1551758	Pygo2	pygopus 2	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:19487454
1551758	Pygo2	pygopus 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17458864
1551758	Pygo2	pygopus 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551758	Pygo2	pygopus 2	gene	MP:0012168	abnormal optic placode morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551758	Pygo2	pygopus 2	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:17425782
1551758	Pygo2	pygopus 2	gene	MP:0030242	small optic pit		IAGP		N	RGD:5509061	20200310	MGI			PMID:17428831
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38185096
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0001322	abnormal iris morphology		IEA		N	RGD:5509061	20241121	MGI			
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20240801	MGI			PMID:38185096
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38185096
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20240801	MGI			PMID:38185096
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20240801	MGI			PMID:38185096
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20240801	MGI			PMID:38185096
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20241121	MGI			
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250220	MGI			PMID:38185096
1551760	Tspyl5	testis-specific protein, Y-encoded-like 5	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38185096
1551766	Rcn1	reticulocalbin 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1551766	Rcn1	reticulocalbin 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20220811	MGI			
1551766	Rcn1	reticulocalbin 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201231	MGI			
1551766	Rcn1	reticulocalbin 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210826	MGI			
1551766	Rcn1	reticulocalbin 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20250508	MGI			
1551766	Rcn1	reticulocalbin 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1551766	Rcn1	reticulocalbin 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20200310	MGI			
1551766	Rcn1	reticulocalbin 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1551766	Rcn1	reticulocalbin 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20200310	MGI			
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141009	MGI			PMID:23636094
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0003211	abnormal aorta elastic fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0003279	aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0003705	abnormal hypodermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0005421	loose skin		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0005489	vascular smooth muscle hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0006135	artery stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141009	MGI			PMID:23636094
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0006265	increased pulse pressure		IAGP		N	RGD:5509061	20141009	MGI			PMID:23636094
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0008418	abnormal cutaneous elastic fiber morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:23636094
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009866	abnormal aorta wall morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:23636094
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:23636094
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009869	abnormal descending aorta morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17311093
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010202	focal dorsal hair loss		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010470	dilated ascending aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010470	dilated ascending aorta		IAGP		N	RGD:5509061	20141009	MGI			PMID:23636094
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010641	descending aorta stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010661	ascending aorta aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010661	ascending aorta aneurysm		IAGP		N	RGD:5509061	20141009	MGI			PMID:23636094
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010661	ascending aorta aneurysm		IAGP		N	RGD:5509061	20210617	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010661	ascending aorta aneurysm		IAGP		N	RGD:5509061	20210617	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20141009	MGI			PMID:23636094
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855011
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16478991
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0011157	abnormal hypodermis muscle layer morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0011575	dilated aorta bulb		IAGP		N	RGD:5509061	20210617	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20150917	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0020161	increased vascular endothelial cell proliferation		IAGP		N	RGD:5509061	20160616	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0020321	increased vascular endothelial cell apoptosis		IAGP		N	RGD:5509061	20160616	MGI			PMID:20019329
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0031086	wheezing		IAGP		N	RGD:5509061	20200709	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0031132	increased artery tortuosity		IAGP		N	RGD:5509061	20210617	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0031134	increased carotid artery tortuosity		IAGP		N	RGD:5509061	20210617	MGI			PMID:26178373
1551771	Efemp2	epidermal growth factor-containing fibulin-like extracellular matrix protein 2	gene	MP:0031510	increased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:20019329
1551781	Prune1	prune exopolyphosphatase	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20111116	MGI			
1551781	Prune1	prune exopolyphosphatase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551781	Prune1	prune exopolyphosphatase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1551782	Cnot6	CCR4-NOT transcription complex, subunit 6	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20210513	MGI			PMID:31924127
1551782	Cnot6	CCR4-NOT transcription complex, subunit 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210513	MGI			PMID:31924127
1551782	Cnot6	CCR4-NOT transcription complex, subunit 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210805	MGI			PMID:34026442
1551782	Cnot6	CCR4-NOT transcription complex, subunit 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0004850	abnormal testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551783	Cnbd2	cyclic nucleotide binding domain containing 2	gene	MP:0013209	abnormal motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24339785
1551784	Tars1	threonyl-tRNA synthetase 1	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20251211	MGI			PMID:38956874
1551784	Tars1	threonyl-tRNA synthetase 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20251211	MGI			PMID:38956874
1551784	Tars1	threonyl-tRNA synthetase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20251211	MGI			PMID:38956874
1551784	Tars1	threonyl-tRNA synthetase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20251211	MGI			PMID:38956874
1551784	Tars1	threonyl-tRNA synthetase 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20251211	MGI			PMID:38956874
1551784	Tars1	threonyl-tRNA synthetase 1	gene	MP:0010202	focal dorsal hair loss		IAGP		N	RGD:5509061	20251211	MGI			PMID:38956874
1551784	Tars1	threonyl-tRNA synthetase 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20251211	MGI			PMID:38956874
1551784	Tars1	threonyl-tRNA synthetase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927618
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126735
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210826	MGI			
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502824
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072562
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126735
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12742262
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20201231	MGI			
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502824
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072562
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502824
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14997009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126735
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072562
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927618
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072562
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072562
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12000791
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12000791
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002570	alcohol aversion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15203244
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126735
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072562
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11579129
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16650144
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305161
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305161
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17272395
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502824
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305161
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927618
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005137	increased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17272395
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126735
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126735
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072562
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:12072562
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950139
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12126735
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305161
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20250306	MGI			PMID:11579129
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502824
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12453895
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11927618
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16650144
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0011021	abnormal circadian regulation of heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10502824
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0011385	abnormal testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17272395
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15203244
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16364461
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0014145	increased white adipose tissue mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20160407	MGI			PMID:20613867
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:14997009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0014441	decreased response to leptin		IAGP		N	RGD:5509061	20240613	MGI			PMID:10502824
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0014567	increased circulating pancreatic peptide level		IAGP		N	RGD:5509061	20241128	MGI			PMID:12072562
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0014567	increased circulating pancreatic peptide level		IAGP		N	RGD:5509061	20241128	MGI			PMID:12861009
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0014638	increased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:11579129
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:11927618
1551786	Npy2r	neuropeptide Y receptor Y2	gene	MP:0020080	increased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:11927618
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395638
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395638
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395638
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395638
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395638
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395638
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0008285	abnormal hippocampus granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0008440	abnormal subplate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395638
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395638
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409883
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22095278
1551787	Zbtb18	zinc finger and BTB domain containing 18	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:22095278
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20180712	MGI			PMID:28665968
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20180712	MGI			PMID:28665968
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0001671	abnormal vitamin absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180712	MGI			PMID:28665968
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20180712	MGI			PMID:28665968
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20180712	MGI			PMID:28665968
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20180712	MGI			PMID:28665968
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0009860	nephrosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0011226	abnormal thiamin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879271
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0011226	abnormal thiamin level		IAGP		N	RGD:5509061	20180712	MGI			PMID:28665968
1551788	Slc19a3	solute carrier family 19, member 3	gene	MP:0031301	chronic liver inflammation		IAGP		N	RGD:5509061	20211028	MGI			PMID:19879271
1551792	Usf1	upstream transcription factor 1	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520440
1551792	Usf1	upstream transcription factor 1	gene	MP:0001446	abnormal whisker trimming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520440
1551792	Usf1	upstream transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9685363
1551792	Usf1	upstream transcription factor 1	gene	MP:0002808	abnormal barbering behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520440
1551792	Usf1	upstream transcription factor 1	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520440
1551792	Usf1	upstream transcription factor 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520440
1551792	Usf1	upstream transcription factor 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520440
1551792	Usf1	upstream transcription factor 1	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:23580255
1551792	Usf1	upstream transcription factor 1	gene	MP:0020468	abnormal circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:23580255
1551792	Usf1	upstream transcription factor 1	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:23580255
1551794	Iqce	IQ motif containing E	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1551794	Iqce	IQ motif containing E	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20200310	MGI			
1551794	Iqce	IQ motif containing E	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20200310	MGI			
1551794	Iqce	IQ motif containing E	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1551794	Iqce	IQ motif containing E	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1551794	Iqce	IQ motif containing E	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1551794	Iqce	IQ motif containing E	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1551794	Iqce	IQ motif containing E	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1551794	Iqce	IQ motif containing E	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1551794	Iqce	IQ motif containing E	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0009837	abnormal sperm end piece morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0031352	absent sperm axonemal central pair		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551800	Styxl1	serine/threonine/tyrosine interacting-like 1	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20240808	MGI			PMID:38168070
1551801	Neil3	nei like 3 (E. coli)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:16428305
1551801	Neil3	nei like 3 (E. coli)	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22065741
1551801	Neil3	nei like 3 (E. coli)	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22065741
1551801	Neil3	nei like 3 (E. coli)	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22065741
1551801	Neil3	nei like 3 (E. coli)	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20200310	MGI			PMID:22065741
1551801	Neil3	nei like 3 (E. coli)	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22065741
1551801	Neil3	nei like 3 (E. coli)	gene	MP:0020449	decreased microglial cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22065741
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20221215	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20221215	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20221215	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0000690	absent spleen		IEA		N	RGD:5509061	20111116	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20221215	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20221215	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20221215	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20221215	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20221215	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1551802	Pcgf3	polycomb group ring finger 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1551806	Zc3h14	zinc finger CCCH type containing 14	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20180118	MGI			PMID:28666327
1551806	Zc3h14	zinc finger CCCH type containing 14	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20211021	MGI			
1551806	Zc3h14	zinc finger CCCH type containing 14	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210520	MGI			
1551806	Zc3h14	zinc finger CCCH type containing 14	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20180118	MGI			PMID:28666327
1551806	Zc3h14	zinc finger CCCH type containing 14	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20180118	MGI			PMID:28666327
1551806	Zc3h14	zinc finger CCCH type containing 14	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20180118	MGI			PMID:28666327
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20200310	MGI			
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200310	MGI			
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20200310	MGI			
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20200310	MGI			
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0010093	decreased circulating magnesium level		IEA		N	RGD:5509061	20200310	MGI			
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551807	Dusp26	dual specificity phosphatase 26	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30582764
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20210422	MGI			PMID:27061115
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210422	MGI			PMID:27061115
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20210422	MGI			PMID:27061115
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210422	MGI			PMID:27061115
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0004039	abnormal cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:24078630
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210422	MGI			PMID:27061115
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1551808	Lmbrd1	LMBR1 domain containing 1	gene	MP:0030018	increased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:24078630
1551809	Acaa2	acetyl-CoA acyltransferase 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20250508	MGI			
1551810	Cd226	CD226 antigen	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029380
1551810	Cd226	CD226 antigen	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029379
1551810	Cd226	CD226 antigen	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029380
1551810	Cd226	CD226 antigen	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:24658051
1551810	Cd226	CD226 antigen	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029379
1551810	Cd226	CD226 antigen	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24658051
1551810	Cd226	CD226 antigen	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029380
1551810	Cd226	CD226 antigen	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029379
1551810	Cd226	CD226 antigen	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029379
1551810	Cd226	CD226 antigen	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029380
1551810	Cd226	CD226 antigen	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029379
1551810	Cd226	CD226 antigen	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029380
1551810	Cd226	CD226 antigen	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029380
1551810	Cd226	CD226 antigen	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029380
1551810	Cd226	CD226 antigen	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:19029379
1551812	Sypl1	synaptophysin like 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20231207	MGI			
1551812	Sypl1	synaptophysin like 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20231207	MGI			
1551812	Sypl1	synaptophysin like 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0014239	abnormal intracellular organelle morphology		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551812	Sypl1	synaptophysin like 1	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20230914	MGI			PMID:37607933
1551816	Tox3	TOX high mobility group box family member 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1551816	Tox3	TOX high mobility group box family member 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20200310	MGI			
1551820	Lrrc8e	leucine rich repeat containing 8 family, member E	gene	MP:0002418	increased susceptibility to viral infection		IAGP		N	RGD:5509061	20201001	MGI			PMID:32277911
1551820	Lrrc8e	leucine rich repeat containing 8 family, member E	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20201001	MGI			PMID:32277911
1551820	Lrrc8e	leucine rich repeat containing 8 family, member E	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20201001	MGI			PMID:32277911
1551820	Lrrc8e	leucine rich repeat containing 8 family, member E	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20201001	MGI			PMID:32277911
1551820	Lrrc8e	leucine rich repeat containing 8 family, member E	gene	MP:0009791	increased susceptibility to viral infection induced morbidity/mortality		IAGP		N	RGD:5509061	20201001	MGI			PMID:32277911
1551820	Lrrc8e	leucine rich repeat containing 8 family, member E	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20201001	MGI			PMID:32277911
1551820	Lrrc8e	leucine rich repeat containing 8 family, member E	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20201001	MGI			PMID:32277911
1551821	Nfkbil1	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor like 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160114	MGI			
1551821	Nfkbil1	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor like 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160114	MGI			
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808086
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951074
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0000757	herniated abdominal wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951074
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951074
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20221215	MGI			
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951074
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951074
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951074
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004627	abnormal trochanter morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004675	rib fractures		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004987	abnormal osteoblast cell number		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951074
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808086
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808086
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808086
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8951074
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808086
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0011643	abnormal tendon collagen fibril morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0013626	decreased femur yield load		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0013633	decreased femur maximal load		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0013638	decreased femur stiffness		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0013646	decreased energy dissipated prior to femur fracture		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0013941	abnormal enthesis morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20151112	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0030484	abnormal osteocyte lacuna morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0030487	abnormal osteocyte dendritic process morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:24419319
1551822	Bmp1	bone morphogenetic protein 1	gene	MP:0030827	femur fracture		IAGP		N	RGD:5509061	20181018	MGI			PMID:24419319
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20231207	MGI			
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:11078464
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20231207	MGI			
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21998599
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0004836	abnormal synaptic acetylcholine release		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20231207	MGI			
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21998599
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20200310	MGI			PMID:24744148
1551824	Stxbp5l	syntaxin binding protein 5-like	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20231207	MGI			
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0000520	absent kidney		IEA		N	RGD:5509061	20150903	MGI			
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20111116	MGI			
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20111116	MGI			
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0003051	curly tail		IEA		N	RGD:5509061	20111116	MGI			
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0004385	interparietal bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0004674	thin ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0009160	abnormal pancreatic acinar cell zymogen granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0010161	decreased brain cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0010422	heart right ventricle hypoplasia		IEA		N	RGD:5509061	20150903	MGI			
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0030252	narrow frontonasal prominence		IAGP		N	RGD:5509061	20171026	MGI			PMID:12812989
1551825	Sc5d	sterol-C5-desaturase	gene	MP:0030256	abnormal mandibular dental arch morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:12812989
1551829	Dnai4	dynein axonemal intermediate chain 4	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230601	MGI			
1551829	Dnai4	dynein axonemal intermediate chain 4	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1551832	Cklf	chemokine-like factor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20220120	MGI			PMID:34446558
1551835	Smn1	survival motor neuron 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:21249120
1551835	Smn1	survival motor neuron 1	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21672919
1551835	Smn1	survival motor neuron 1	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:10655541
1551835	Smn1	survival motor neuron 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:10655541
1551835	Smn1	survival motor neuron 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:10655541
1551835	Smn1	survival motor neuron 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19329542
1551835	Smn1	survival motor neuron 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:10655541
1551835	Smn1	survival motor neuron 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:15076752
1551835	Smn1	survival motor neuron 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:12091709
1551835	Smn1	survival motor neuron 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15703193
1551835	Smn1	survival motor neuron 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178576
1551835	Smn1	survival motor neuron 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497369
1551835	Smn1	survival motor neuron 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0001007	abnormal sympathetic system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20200310	MGI			PMID:18065780
1551835	Smn1	survival motor neuron 1	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15703193
1551835	Smn1	survival motor neuron 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18065780
1551835	Smn1	survival motor neuron 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15076752
1551835	Smn1	survival motor neuron 1	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15076752
1551835	Smn1	survival motor neuron 1	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0001212	skin lesions		IEA		N	RGD:5509061	20111116	MGI			
1551835	Smn1	survival motor neuron 1	gene	MP:0001220	epidermal necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0001220	epidermal necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:15703193
1551835	Smn1	survival motor neuron 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:15076752
1551835	Smn1	survival motor neuron 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497369
1551835	Smn1	survival motor neuron 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497369
1551835	Smn1	survival motor neuron 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21672919
1551835	Smn1	survival motor neuron 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:20705738
1551835	Smn1	survival motor neuron 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:21672919
1551835	Smn1	survival motor neuron 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:15703193
1551835	Smn1	survival motor neuron 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497369
1551835	Smn1	survival motor neuron 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:10655541
1551835	Smn1	survival motor neuron 1	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20200310	MGI			PMID:15703193
1551835	Smn1	survival motor neuron 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:15703193
1551835	Smn1	survival motor neuron 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15703193
1551835	Smn1	survival motor neuron 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9275227
1551835	Smn1	survival motor neuron 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:21249120
1551835	Smn1	survival motor neuron 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:10655541
1551835	Smn1	survival motor neuron 1	gene	MP:0001956	hypopnea		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:15076752
1551835	Smn1	survival motor neuron 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:15076752
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178576
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497369
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21672919
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9275227
1551835	Smn1	survival motor neuron 1	gene	MP:0002088	abnormal embryonic growth/weight/body size		IEA		N	RGD:5509061	20111116	MGI			
1551835	Smn1	survival motor neuron 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20111116	MGI			
1551835	Smn1	survival motor neuron 1	gene	MP:0002102	abnormal ear morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21672919
1551835	Smn1	survival motor neuron 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0002314	abnormal respiratory mechanics		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20200310	MGI			PMID:9275227
1551835	Smn1	survival motor neuron 1	gene	MP:0002738	hyperresponsive to tactile stimuli		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:20705738
1551835	Smn1	survival motor neuron 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0002883	chromatolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0002913	abnormal PNS synaptic transmission		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19329542
1551835	Smn1	survival motor neuron 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0003201	extremity edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0003466	decreased single cell response threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0003928	increased heart rate variability		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9275227
1551835	Smn1	survival motor neuron 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497369
1551835	Smn1	survival motor neuron 1	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0004243	abnormal motor nerve collateral sprouting		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20200310	MGI			PMID:10655541
1551835	Smn1	survival motor neuron 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0005356	positive geotaxis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:15076752
1551835	Smn1	survival motor neuron 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0005407	hyperalgesia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0005576	decreased pulmonary ventilation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0006404	abnormal lumbar dorsal root ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178576
1551835	Smn1	survival motor neuron 1	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0008142	decreased small intestinal villus size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20705738
1551835	Smn1	survival motor neuron 1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178576
1551835	Smn1	survival motor neuron 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20200310	MGI			PMID:18065780
1551835	Smn1	survival motor neuron 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:15703193
1551835	Smn1	survival motor neuron 1	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19497369
1551835	Smn1	survival motor neuron 1	gene	MP:0009703	decreased birth body size		IEA		N	RGD:5509061	20111116	MGI			
1551835	Smn1	survival motor neuron 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:20705738
1551835	Smn1	survival motor neuron 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11238465
1551835	Smn1	survival motor neuron 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0010506	prolonged RR interval		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:23390132
1551835	Smn1	survival motor neuron 1	gene	MP:0010900	abnormal pulmonary interalveolar septum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23263861
1551835	Smn1	survival motor neuron 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10655541
1551835	Smn1	survival motor neuron 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15703193
1551835	Smn1	survival motor neuron 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178576
1551835	Smn1	survival motor neuron 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19329542
1551835	Smn1	survival motor neuron 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20693262
1551835	Smn1	survival motor neuron 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20826664
1551835	Smn1	survival motor neuron 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21672919
1551835	Smn1	survival motor neuron 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22423102
1551835	Smn1	survival motor neuron 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20085811
1551835	Smn1	survival motor neuron 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1551835	Smn1	survival motor neuron 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10655541
1551835	Smn1	survival motor neuron 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19329542
1551835	Smn1	survival motor neuron 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10749994
1551835	Smn1	survival motor neuron 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12515823
1551835	Smn1	survival motor neuron 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9275227
1551835	Smn1	survival motor neuron 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21249120
1551835	Smn1	survival motor neuron 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21249120
1551835	Smn1	survival motor neuron 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20696672
1551835	Smn1	survival motor neuron 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21249120
1551835	Smn1	survival motor neuron 1	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29371219
1551835	Smn1	survival motor neuron 1	gene	MP:0013178	tail necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10615130
1551835	Smn1	survival motor neuron 1	gene	MP:0013178	tail necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178576
1551835	Smn1	survival motor neuron 1	gene	MP:0013178	tail necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22802075
1551835	Smn1	survival motor neuron 1	gene	MP:0014709	abnormal synaptic vesicle readily releasable pool size		IAGP		N	RGD:5509061	20250814	MGI			PMID:23263861
1551837	Zfp689	zinc finger protein 689	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1551837	Zfp689	zinc finger protein 689	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20181227	MGI			
1551837	Zfp689	zinc finger protein 689	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20260402	MGI			
1551837	Zfp689	zinc finger protein 689	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20211021	MGI			
1551837	Zfp689	zinc finger protein 689	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1551837	Zfp689	zinc finger protein 689	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551837	Zfp689	zinc finger protein 689	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20170105	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210128	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:22284184
1551840	Prdm8	PR domain containing 8	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20210128	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20220519	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20200310	MGI			PMID:22284184
1551840	Prdm8	PR domain containing 8	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22284184
1551840	Prdm8	PR domain containing 8	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20210520	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20200310	MGI			PMID:22284184
1551840	Prdm8	PR domain containing 8	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20210128	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20210826	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210128	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20200310	MGI			PMID:22284184
1551840	Prdm8	PR domain containing 8	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20210128	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20260402	MGI			
1551840	Prdm8	PR domain containing 8	gene	MP:0014747	abnormal motor neuron axon guidance		IAGP		N	RGD:5509061	20250904	MGI			PMID:22284184
1551840	Prdm8	PR domain containing 8	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1551842	Dlst	dihydrolipoamide S-succinyltransferase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596066
1551842	Dlst	dihydrolipoamide S-succinyltransferase	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596066
1551842	Dlst	dihydrolipoamide S-succinyltransferase	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:19596066
1551842	Dlst	dihydrolipoamide S-succinyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1551843	Sf3b3	splicing factor 3b, subunit 3	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201022	MGI			
1551843	Sf3b3	splicing factor 3b, subunit 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1551843	Sf3b3	splicing factor 3b, subunit 3	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1551843	Sf3b3	splicing factor 3b, subunit 3	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1551843	Sf3b3	splicing factor 3b, subunit 3	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201022	MGI			
1551843	Sf3b3	splicing factor 3b, subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551843	Sf3b3	splicing factor 3b, subunit 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551843	Sf3b3	splicing factor 3b, subunit 3	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1551847	Uqcrc1	ubiquinol-cytochrome c reductase core protein 1	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20200423	MGI			PMID:30666338
1551847	Uqcrc1	ubiquinol-cytochrome c reductase core protein 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20200423	MGI			PMID:30666338
1551847	Uqcrc1	ubiquinol-cytochrome c reductase core protein 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20200423	MGI			PMID:30666338
1551847	Uqcrc1	ubiquinol-cytochrome c reductase core protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200423	MGI			PMID:30666338
1551847	Uqcrc1	ubiquinol-cytochrome c reductase core protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1551847	Uqcrc1	ubiquinol-cytochrome c reductase core protein 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200423	MGI			PMID:30666338
1551847	Uqcrc1	ubiquinol-cytochrome c reductase core protein 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0005415	intrahepatic cholestasis		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0008447	absent retina cone cells		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0009773	absent retina		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200109	MGI			PMID:28839191
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551850	Cdc50a	cell division cycle 50 P4-ATPase accessory subunit A	gene	MP:0020211	slow movement		IAGP		N	RGD:5509061	20180315	MGI			PMID:28919113
1551852	Crb2	crumbs family member 2	gene	MP:0000474	abnormal foregut morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0001699	increased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1551852	Crb2	crumbs family member 2	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1551852	Crb2	crumbs family member 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20200310	MGI			
1551852	Crb2	crumbs family member 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1551852	Crb2	crumbs family member 2	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0004559	small allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0008105	increased amacrine cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0008452	increased retina rod cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1551852	Crb2	crumbs family member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551852	Crb2	crumbs family member 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0011964	increased total retina thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0012081	absent heart tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0012104	small amniotic cavity		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0012739	abnormal anterior primitive streak morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22072575
1551852	Crb2	crumbs family member 2	gene	MP:0014333	short retina cone cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:24493795
1551852	Crb2	crumbs family member 2	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0030006	decreased retina apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24339791
1551852	Crb2	crumbs family member 2	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:23001562
1551852	Crb2	crumbs family member 2	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:24493795
1551853	Atf6b	activating transcription factor 6 beta	gene	MP:0001192	scaly skin		IEA		N	RGD:5509061	20181227	MGI			
1551853	Atf6b	activating transcription factor 6 beta	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1551853	Atf6b	activating transcription factor 6 beta	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765680
1551853	Atf6b	activating transcription factor 6 beta	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765680
1551853	Atf6b	activating transcription factor 6 beta	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551854	Rps9	ribosomal protein S9	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0003587	ureter obstruction		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0010951	abnormal lipid oxidation		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551854	Rps9	ribosomal protein S9	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20221201	MGI			PMID:35235349
1551855	Insrr	insulin receptor-related receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
1551855	Insrr	insulin receptor-related receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
1551855	Insrr	insulin receptor-related receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
1551855	Insrr	insulin receptor-related receptor	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628051
1551855	Insrr	insulin receptor-related receptor	gene	MP:0002893	ketoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
1551855	Insrr	insulin receptor-related receptor	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:14628051
1551855	Insrr	insulin receptor-related receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
1551855	Insrr	insulin receptor-related receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11463843
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000777	increased inferior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389662
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389662
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389662
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:1401878
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389662
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1401878
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:1401878
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0000899	abnormal corpora quadrigemina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723533
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001063	abnormal trochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723533
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723533
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1401878
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:1401878
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1401878
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1401878
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:1401878
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389662
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389662
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0006097	abnormal cerebellar lobule formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0009681	abnormal pyramidal decussation morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12451134
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126743
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0009957	abnormal cerebellum vermis lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9550145
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0009960	abnormal cerebellum anterior lobe morphology		IEA		N	RGD:5509061	20111116	MGI			
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723533
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1401878
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:14562603
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0012055	abnormal phrenic nerve innervation pattern to diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16723533
1551856	Unc5c	unc-5 netrin receptor C	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:14562603
1551857	Tusc3	tumor suppressor candidate 3	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1551857	Tusc3	tumor suppressor candidate 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1551857	Tusc3	tumor suppressor candidate 3	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20190502	MGI			
1551857	Tusc3	tumor suppressor candidate 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0002916	increased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551861	Sh3gl3	SH3-domain GRB2-like 3	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:22099461
1551863	Trpm4	transient receptor potential cation channel, subfamily M, member 4	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758465
1551863	Trpm4	transient receptor potential cation channel, subfamily M, member 4	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293867
1551863	Trpm4	transient receptor potential cation channel, subfamily M, member 4	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293867
1551863	Trpm4	transient receptor potential cation channel, subfamily M, member 4	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17293867
1551863	Trpm4	transient receptor potential cation channel, subfamily M, member 4	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18758465
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201231	MGI			
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210422	MGI			
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20241121	MGI			
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20241121	MGI			
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19138685
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20493170
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20210422	MGI			
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19138685
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210422	MGI			
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19138685
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:19138685
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0014698	decreased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:19138685
1551864	Fndc3b	fibronectin type III domain containing 3B	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:20493170
1551867	Zfp532	zinc finger protein 532	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1551867	Zfp532	zinc finger protein 532	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1551867	Zfp532	zinc finger protein 532	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1551867	Zfp532	zinc finger protein 532	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1551867	Zfp532	zinc finger protein 532	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1551867	Zfp532	zinc finger protein 532	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1551867	Zfp532	zinc finger protein 532	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20230601	MGI			
1551867	Zfp532	zinc finger protein 532	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1551867	Zfp532	zinc finger protein 532	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1551869	Nqo2	N-ribosyldihydronicotinamide quinone reductase 2	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351651
1551869	Nqo2	N-ribosyldihydronicotinamide quinone reductase 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861374
1551869	Nqo2	N-ribosyldihydronicotinamide quinone reductase 2	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351651
1551869	Nqo2	N-ribosyldihydronicotinamide quinone reductase 2	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861374
1551869	Nqo2	N-ribosyldihydronicotinamide quinone reductase 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351651
1551869	Nqo2	N-ribosyldihydronicotinamide quinone reductase 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12351651
1551869	Nqo2	N-ribosyldihydronicotinamide quinone reductase 2	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:20861374
1551869	Nqo2	N-ribosyldihydronicotinamide quinone reductase 2	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342368
1551869	Nqo2	N-ribosyldihydronicotinamide quinone reductase 2	gene	MP:0014368	enhanced long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:20861374
1551873	Wwp1	WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1551873	Wwp1	WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210826	MGI			
1551873	Wwp1	WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20200402	MGI			
1551873	Wwp1	WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21809421
1551873	Wwp1	WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1551875	Vamp7	vesicle-associated membrane protein 7	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22323709
1551875	Vamp7	vesicle-associated membrane protein 7	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22323709
1551875	Vamp7	vesicle-associated membrane protein 7	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22323709
1551875	Vamp7	vesicle-associated membrane protein 7	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21740490
1551875	Vamp7	vesicle-associated membrane protein 7	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22323709
1551876	Brd2	bromodomain containing 2	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0000141	abnormal vertebral body morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000153	rib bifurcation		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000161	scoliosis		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19301389
1551876	Brd2	bromodomain containing 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19301389
1551876	Brd2	bromodomain containing 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0000480	increased rib number		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000632	abnormal pineal gland morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0000820	abnormal choroid plexus morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0001014	absent superior cervical ganglion		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0001100	abnormal vagus ganglion morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0001697	abnormal embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19301389
1551876	Brd2	bromodomain containing 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19301389
1551876	Brd2	bromodomain containing 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0002239	abnormal nasal septum morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0002746	abnormal semilunar valve morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0002747	abnormal aortic valve morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0002748	abnormal pulmonary valve morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0002951	small thyroid gland		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19301389
1551876	Brd2	bromodomain containing 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0003078	aphakia		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0003345	decreased rib number		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0003387	aorta coarctation		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19301389
1551876	Brd2	bromodomain containing 2	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0004057	thin myocardium compact layer		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004110	transposition of great arteries		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004163	abnormal adenohypophysis morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004201	fetal growth retardation		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004571	absent vagus nerve		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004603	absent vertebral arch		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0005105	abnormal middle ear ossicle morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0005236	abnormal olfactory nerve morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20181227	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0006135	artery stenosis		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0009167	increased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0009770	abnormal optic chiasm morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0010496	abnormal pectinate muscle morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0010572	persistent right dorsal aorta		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0010589	common truncal valve		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0010853	abnormal lung position or orientation		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19883376
1551876	Brd2	bromodomain containing 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19301389
1551876	Brd2	bromodomain containing 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0011380	enlarged brain ventricles		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0011659	interrupted aortic arch, type b		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0012548	myelocele		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0012702	increased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22885183
1551876	Brd2	bromodomain containing 2	gene	MP:0012729	abnormal common carotid artery morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:19301389
1551876	Brd2	bromodomain containing 2	gene	MP:0013809	absent pectinate muscle		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013814	abnormal hepatic portal vein connection		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013847	retropleural edema		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013852	abnormal Mullerian duct topology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013873	abnormal ductus venosus morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013874	abnormal ductus venosus topology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013879	duplication of ductus venosus		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013913	absent costovertebral joint		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013929	absent eye muscles		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013936	abnormal thymus topology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013985	abnormal umbilical vein topology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0013995	abnormal external carotid artery origin		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0020483	abnormal brain artery topology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0020502	abnormal physiological umbilical hernia morphology		IEA		N	RGD:5509061	20180628	MGI			
1551876	Brd2	bromodomain containing 2	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:19883376
1551878	Lcn8	lipocalin 8	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210603	MGI			PMID:33631677
1551878	Lcn8	lipocalin 8	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20210603	MGI			PMID:33631677
1551878	Lcn8	lipocalin 8	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33631677
1551878	Lcn8	lipocalin 8	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20210603	MGI			PMID:33631677
1551878	Lcn8	lipocalin 8	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20210603	MGI			PMID:33631677
1551878	Lcn8	lipocalin 8	gene	MP:0013288	premature acrosome reaction		IAGP		N	RGD:5509061	20210603	MGI			PMID:33631677
1551878	Lcn8	lipocalin 8	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210603	MGI			PMID:33631677
1551879	Cpa6	carboxypeptidase A6	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1551879	Cpa6	carboxypeptidase A6	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20241121	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20201022	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20200310	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20200310	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200310	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20200310	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19914232
1551880	Foxj3	forkhead box J3	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:19914232
1551880	Foxj3	forkhead box J3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19914232
1551880	Foxj3	forkhead box J3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19914232
1551880	Foxj3	forkhead box J3	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20211021	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0004246	abnormal extensor digitorum longus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19914232
1551880	Foxj3	forkhead box J3	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:19914232
1551880	Foxj3	forkhead box J3	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19914232
1551880	Foxj3	forkhead box J3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20200310	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20200310	MGI			
1551880	Foxj3	forkhead box J3	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:19914232
1551881	Icam2	intercellular adhesion molecule 2	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10023766
1551881	Icam2	intercellular adhesion molecule 2	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10023766
1551881	Icam2	intercellular adhesion molecule 2	gene	MP:0002465	abnormal eosinophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10023766
1551885	Dsc3	desmocollin 3	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0001217	absent epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20181227	MGI			
1551885	Dsc3	desmocollin 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1551885	Dsc3	desmocollin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16418220
1551885	Dsc3	desmocollin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0004241	acantholysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1551885	Dsc3	desmocollin 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682494
1551885	Dsc3	desmocollin 3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16418220
1551885	Dsc3	desmocollin 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551885	Dsc3	desmocollin 3	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1551885	Dsc3	desmocollin 3	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1551885	Dsc3	desmocollin 3	gene	MP:0030578	decreased keratinocyte adhesion		IAGP		N	RGD:5509061	20180607	MGI			PMID:18682494
1551886	Tspan13	tetraspanin 13	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20230601	MGI			
1551886	Tspan13	tetraspanin 13	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1551886	Tspan13	tetraspanin 13	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1551886	Tspan13	tetraspanin 13	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1551886	Tspan13	tetraspanin 13	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1551886	Tspan13	tetraspanin 13	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1551886	Tspan13	tetraspanin 13	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1551886	Tspan13	tetraspanin 13	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1551887	Klhl9	kelch-like 9	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1551887	Klhl9	kelch-like 9	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1551887	Klhl9	kelch-like 9	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1551887	Klhl9	kelch-like 9	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1551887	Klhl9	kelch-like 9	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1551889	Krt1	keratin 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16528356
1551889	Krt1	keratin 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16528356
1551889	Krt1	keratin 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:16528356
1551889	Krt1	keratin 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375063
1551889	Krt1	keratin 1	gene	MP:0001230	epidermal desquamation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16528356
1551889	Krt1	keratin 1	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375063
1551889	Krt1	keratin 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16528356
1551889	Krt1	keratin 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375063
1551889	Krt1	keratin 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16528356
1551889	Krt1	keratin 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16528356
1551889	Krt1	keratin 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16528356
1551889	Krt1	keratin 1	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375063
1551889	Krt1	keratin 1	gene	MP:0004930	small epididymis		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20250508	MGI			
1551889	Krt1	keratin 1	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0008588	abnormal circulating interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0009594	abnormal corneocyte envelope morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375063
1551889	Krt1	keratin 1	gene	MP:0009594	abnormal corneocyte envelope morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16528356
1551889	Krt1	keratin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22375063
1551889	Krt1	keratin 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23132931
1551889	Krt1	keratin 1	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20240523	MGI			
1551889	Krt1	keratin 1	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20240523	MGI			
1551890	Dhps	deoxyhypusine synthase	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20170706	MGI			PMID:26037925
1551890	Dhps	deoxyhypusine synthase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200521	MGI			PMID:21850436
1551890	Dhps	deoxyhypusine synthase	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20170706	MGI			PMID:26037925
1551890	Dhps	deoxyhypusine synthase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170706	MGI			PMID:26037925
1551890	Dhps	deoxyhypusine synthase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170706	MGI			PMID:26037925
1551890	Dhps	deoxyhypusine synthase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160804	MGI			PMID:21389784
1551890	Dhps	deoxyhypusine synthase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20170706	MGI			PMID:26037925
1551890	Dhps	deoxyhypusine synthase	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1551890	Dhps	deoxyhypusine synthase	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20170706	MGI			PMID:26037925
1551890	Dhps	deoxyhypusine synthase	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20200521	MGI			PMID:21850436
1551890	Dhps	deoxyhypusine synthase	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20170706	MGI			PMID:26037925
1551890	Dhps	deoxyhypusine synthase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170706	MGI			PMID:26037925
1551890	Dhps	deoxyhypusine synthase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160804	MGI			PMID:21389784
1551890	Dhps	deoxyhypusine synthase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200521	MGI			PMID:21850436
1551890	Dhps	deoxyhypusine synthase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31780266
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20201217	MGI			PMID:31780266
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20201217	MGI			PMID:31780266
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31780266
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0003182	decreased pulmonary endothelial cell surface		IAGP		N	RGD:5509061	20201217	MGI			PMID:31780266
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0010816	decreased type I pneumocyte number		IAGP		N	RGD:5509061	20201217	MGI			PMID:31780266
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31780266
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0011053	decreased respiratory motile cilia number		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0011071	absent club cells		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201217	MGI			PMID:31780266
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0014200	abnormal respiratory epithelium physiology		IAGP		N	RGD:5509061	20210819	MGI			PMID:31562139
1551892	Wfdc2	WAP four-disulfide core domain 2	gene	MP:0031068	decreased blood oxygen saturation level		IAGP		N	RGD:5509061	20201217	MGI			PMID:31780266
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20190502	MGI			
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0020511	decreased dendritic spine length		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551894	Sh3rf1	SH3 domain containing ring finger 1	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20220721	MGI			PMID:35385725
1551898	Coq2	coenzyme Q2 4-hydroxybenzoate polyprenyltransferase	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20200310	MGI			
1551898	Coq2	coenzyme Q2 4-hydroxybenzoate polyprenyltransferase	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1551898	Coq2	coenzyme Q2 4-hydroxybenzoate polyprenyltransferase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1551898	Coq2	coenzyme Q2 4-hydroxybenzoate polyprenyltransferase	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20200310	MGI			
1551898	Coq2	coenzyme Q2 4-hydroxybenzoate polyprenyltransferase	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200310	MGI			
1551898	Coq2	coenzyme Q2 4-hydroxybenzoate polyprenyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551898	Coq2	coenzyme Q2 4-hydroxybenzoate polyprenyltransferase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1551900	Nanp	N-acetylneuraminic acid phosphatase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1551901	Tmed3	transmembrane p24 trafficking protein 3	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001196	shiny skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0005285	decreased unsaturated fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IEA		N	RGD:5509061	20111116	MGI			
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20191226	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0009608	abnormal epidermal lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0011015	decreased body surface temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551902	Dgat2	diacylglycerol O-acyltransferase 2	gene	MP:0013178	tail necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14668353
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000755
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689653
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000755
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689653
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000755
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000763
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000755
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689653
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0004957	abnormal blastocyst morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000755
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689653
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689653
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0006102	decreased tegmentum size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000763
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689653
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000763
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000755
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000755
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000755
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000763
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0012102	absent trophectoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:22689653
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0012203	abnormal neuronal stem cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23798389
1551904	Gnl3	guanine nucleotide binding protein nucleolar 3	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17000763
1551905	Rab11fip3	RAB11 family interacting protein 3 (class II)	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1551905	Rab11fip3	RAB11 family interacting protein 3 (class II)	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20200310	MGI			
1551905	Rab11fip3	RAB11 family interacting protein 3 (class II)	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20200310	MGI			
1551905	Rab11fip3	RAB11 family interacting protein 3 (class II)	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1551905	Rab11fip3	RAB11 family interacting protein 3 (class II)	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1551905	Rab11fip3	RAB11 family interacting protein 3 (class II)	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1551905	Rab11fip3	RAB11 family interacting protein 3 (class II)	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20230601	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20241121	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20230601	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20241121	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20230601	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1551908	Or1e1c	olfactory receptor family 1 subfamily E member 1C	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20230601	MGI			
1551909	Rab31	RAB31, member RAS oncogene family	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1551913	Prkd1	protein kinase D1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1551913	Prkd1	protein kinase D1	gene	MP:0001629	abnormal heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287012
1551913	Prkd1	protein kinase D1	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1551913	Prkd1	protein kinase D1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287012
1551913	Prkd1	protein kinase D1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287012
1551913	Prkd1	protein kinase D1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287012
1551913	Prkd1	protein kinase D1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1551913	Prkd1	protein kinase D1	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287012
1551913	Prkd1	protein kinase D1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1551913	Prkd1	protein kinase D1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20819079
1551913	Prkd1	protein kinase D1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287012
1551913	Prkd1	protein kinase D1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20819079
1551913	Prkd1	protein kinase D1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20819079
1551913	Prkd1	protein kinase D1	gene	MP:0011730	increased myelin sheath thickness		IAGP		N	RGD:5509061	20260129	MGI			PMID:33904160
1551913	Prkd1	protein kinase D1	gene	MP:0012349	increased susceptibility to induction of seizure by inducing agent		IAGP		N	RGD:5509061	20260129	MGI			PMID:33904160
1551915	Lrrc52	leucine rich repeat containing 52	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20200310	MGI			PMID:25675513
1551915	Lrrc52	leucine rich repeat containing 52	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:25675513
1551915	Lrrc52	leucine rich repeat containing 52	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25675513
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0008371	pituitary intermediate lobe hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0009332	abnormal splenocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22266221
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1551918	Tpx2	TPX2, microtubule-associated	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:22266221
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230601	MGI			
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20230601	MGI			
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230601	MGI			
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:26290337
1551919	Pnkp	polynucleotide kinase 3'- phosphatase	gene	MP:0014768	impaired single-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:26290337
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29977031
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25127365
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:25127365
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20200310	MGI			PMID:25127365
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25127365
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20200310	MGI			PMID:25127365
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:25127365
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0004019	abnormal vitamin homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25127365
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29977031
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25127365
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0005544	cornea deposits		IAGP		N	RGD:5509061	20200310	MGI			PMID:29977031
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29977031
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25127365
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29977031
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551920	Ubiad1	UbiA prenyltransferase domain containing 1	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20200310	MGI			PMID:29977031
1551926	Ankrd45	ankyrin repeat domain 45	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1551928	Nup85	nucleoporin 85	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200903	MGI			PMID:32001710
1551928	Nup85	nucleoporin 85	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200903	MGI			PMID:32001710
1551928	Nup85	nucleoporin 85	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551928	Nup85	nucleoporin 85	gene	MP:0013023	decreased Ly6C high monocyte number		IAGP		N	RGD:5509061	20200903	MGI			PMID:32001710
1551928	Nup85	nucleoporin 85	gene	MP:0013026	decreased Ly6C low monocyte number		IAGP		N	RGD:5509061	20200903	MGI			PMID:32001710
1551929	Nppc	natriuretic peptide type C	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17439653
1551929	Nppc	natriuretic peptide type C	gene	MP:0000592	short tail		IEA		N	RGD:5509061	20111116	MGI			
1551929	Nppc	natriuretic peptide type C	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805384
1551929	Nppc	natriuretic peptide type C	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20111116	MGI			
1551929	Nppc	natriuretic peptide type C	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805384
1551929	Nppc	natriuretic peptide type C	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17439653
1551929	Nppc	natriuretic peptide type C	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20220519	MGI			PMID:22271248
1551929	Nppc	natriuretic peptide type C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17439653
1551929	Nppc	natriuretic peptide type C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220519	MGI			PMID:22271248
1551929	Nppc	natriuretic peptide type C	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20220519	MGI			PMID:22271248
1551929	Nppc	natriuretic peptide type C	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:17439653
1551929	Nppc	natriuretic peptide type C	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20111116	MGI			
1551929	Nppc	natriuretic peptide type C	gene	MP:0002765	short fibula		IEA		N	RGD:5509061	20111116	MGI			
1551929	Nppc	natriuretic peptide type C	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IEA		N	RGD:5509061	20111116	MGI			
1551929	Nppc	natriuretic peptide type C	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20220519	MGI			PMID:22271248
1551929	Nppc	natriuretic peptide type C	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20220519	MGI			PMID:22271248
1551929	Nppc	natriuretic peptide type C	gene	MP:0004686	decreased length of long bones		IEA		N	RGD:5509061	20111116	MGI			
1551929	Nppc	natriuretic peptide type C	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805384
1551929	Nppc	natriuretic peptide type C	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805384
1551929	Nppc	natriuretic peptide type C	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20947764
1551929	Nppc	natriuretic peptide type C	gene	MP:0006394	abnormal vertebral epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20220519	MGI			PMID:22271248
1551929	Nppc	natriuretic peptide type C	gene	MP:0006397	disorganized long bone epiphyseal plate		IEA		N	RGD:5509061	20111116	MGI			
1551929	Nppc	natriuretic peptide type C	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20220519	MGI			PMID:22271248
1551929	Nppc	natriuretic peptide type C	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551929	Nppc	natriuretic peptide type C	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805384
1551929	Nppc	natriuretic peptide type C	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20220519	MGI			PMID:22271248
1551929	Nppc	natriuretic peptide type C	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20220519	MGI			PMID:22271248
1551929	Nppc	natriuretic peptide type C	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17439653
1551929	Nppc	natriuretic peptide type C	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11259675
1551935	Hlx	H2.0-like homeobox	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854219
1551935	Hlx	H2.0-like homeobox	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0001046	abnormal enteric neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854219
1551935	Hlx	H2.0-like homeobox	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854219
1551935	Hlx	H2.0-like homeobox	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0003250	absent gallbladder		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854219
1551935	Hlx	H2.0-like homeobox	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854219
1551935	Hlx	H2.0-like homeobox	gene	MP:0004247	small pancreas		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0004882	enlarged lung		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854219
1551935	Hlx	H2.0-like homeobox	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16854219
1551935	Hlx	H2.0-like homeobox	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0012235	abnormal liver bud morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8557196
1551935	Hlx	H2.0-like homeobox	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:8557196
1551948	Atp13a2	ATPase type 13A2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551948	Atp13a2	ATPase type 13A2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:23393156
1551948	Atp13a2	ATPase type 13A2	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20200310	MGI			PMID:23393156
1551948	Atp13a2	ATPase type 13A2	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:23393156
1551948	Atp13a2	ATPase type 13A2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:23393156
1551948	Atp13a2	ATPase type 13A2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551948	Atp13a2	ATPase type 13A2	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23393156
1551948	Atp13a2	ATPase type 13A2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551948	Atp13a2	ATPase type 13A2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23393156
1551948	Atp13a2	ATPase type 13A2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551948	Atp13a2	ATPase type 13A2	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551948	Atp13a2	ATPase type 13A2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551948	Atp13a2	ATPase type 13A2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20200310	MGI			PMID:23393156
1551948	Atp13a2	ATPase type 13A2	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551948	Atp13a2	ATPase type 13A2	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551948	Atp13a2	ATPase type 13A2	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20200310	MGI			PMID:23393156
1551948	Atp13a2	ATPase type 13A2	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23393156
1551948	Atp13a2	ATPase type 13A2	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551948	Atp13a2	ATPase type 13A2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25855184
1551949	Yif1a	Yip1 interacting factor homolog A (S. cerevisiae)	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1551950	Cav2	caveolin 2	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200204
1551950	Cav2	caveolin 2	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200204
1551950	Cav2	caveolin 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884617
1551950	Cav2	caveolin 2	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884617
1551950	Cav2	caveolin 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1551950	Cav2	caveolin 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884617
1551950	Cav2	caveolin 2	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200204
1551950	Cav2	caveolin 2	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20160915	MGI			PMID:25269481
1551950	Cav2	caveolin 2	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:25269481
1551950	Cav2	caveolin 2	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884617
1551950	Cav2	caveolin 2	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200204
1551950	Cav2	caveolin 2	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20160915	MGI			PMID:25269481
1551950	Cav2	caveolin 2	gene	MP:0010537	tumor regression		IAGP		N	RGD:5509061	20160915	MGI			PMID:25269481
1551950	Cav2	caveolin 2	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884617
1551950	Cav2	caveolin 2	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250403	MGI			PMID:17200204
1551950	Cav2	caveolin 2	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20250925	MGI			PMID:25269481
1551950	Cav2	caveolin 2	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250925	MGI			PMID:25269481
1551951	Ak3	adenylate kinase 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1551954	Uts2b	urotensin 2B	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210520	MGI			
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20241121	MGI			
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962251
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23095888
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0011760	abnormal ureteric bud tip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783789
1551956	Wnt11	wingless-type MMTV integration site family, member 11	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20141218	MGI			PMID:20962251
1551957	Or10a5	olfactory receptor family 10 subfamily A member 5	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186781
1551957	Or10a5	olfactory receptor family 10 subfamily A member 5	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186781
1551958	Cep57l1	centrosomal protein 57-like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551958	Cep57l1	centrosomal protein 57-like 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1551958	Cep57l1	centrosomal protein 57-like 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1551960	Mical2	microtubule associated monooxygenase, calponin and LIM domain containing 2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20231207	MGI			
1551961	Krt25	keratin 25	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920809
1551961	Krt25	keratin 25	gene	MP:0000399	increased curvature of guard hairs		IEA		N	RGD:5509061	20111116	MGI			
1551961	Krt25	keratin 25	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920809
1551961	Krt25	keratin 25	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920809
1551961	Krt25	keratin 25	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920809
1551961	Krt25	keratin 25	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920809
1551961	Krt25	keratin 25	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1551961	Krt25	keratin 25	gene	MP:0002074	abnormal hair texture		IEA		N	RGD:5509061	20111116	MGI			
1551961	Krt25	keratin 25	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16284798
1551961	Krt25	keratin 25	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920809
1551961	Krt25	keratin 25	gene	MP:0008899	plush coat		IEA		N	RGD:5509061	20111116	MGI			
1551961	Krt25	keratin 25	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1551961	Krt25	keratin 25	gene	MP:0010179	rough coat		IEA		N	RGD:5509061	20111116	MGI			
1551961	Krt25	keratin 25	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IEA		N	RGD:5509061	20111116	MGI			
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:6391574
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945695
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16025116
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:6801109
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945695
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945695
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945695
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6801109
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945695
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16025116
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:6391574
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16025116
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6391574
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0003582	abnormal ovary development		IAGP		N	RGD:5509061	20160414	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16025116
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6801109
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20160414	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16025116
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004373	bowed humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004506	abnormal pubis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004507	abnormal ischium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004675	rib fractures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16025116
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:6801109
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0005471	decreased thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0005473	decreased triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0008329	decreased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0008335	decreased gonadotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0008338	decreased thyrotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0008341	decreased corticotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:6801109
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945695
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0010971	abnormal periosteum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945695
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6801109
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8456819
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0013340	abnormal pituicyte morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0014162	decreased circulating cortisol level		IAGP		N	RGD:5509061	20160414	MGI			PMID:15764706
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0030542	abnormal dentin development		IAGP		N	RGD:5509061	20180215	MGI			PMID:16025116
1551964	Smpd3	sphingomyelin phosphodiesterase 3, neutral	gene	MP:0030856	abnormal olecranon morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:8456819
1551965	Nudt19	nudix hydrolase 19	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20170105	MGI			
1551965	Nudt19	nudix hydrolase 19	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1551965	Nudt19	nudix hydrolase 19	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20170105	MGI			
1551965	Nudt19	nudix hydrolase 19	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20231207	MGI			
1551965	Nudt19	nudix hydrolase 19	gene	MP:0005574	decreased pulmonary respiratory rate		IEA		N	RGD:5509061	20231207	MGI			
1551965	Nudt19	nudix hydrolase 19	gene	MP:0005585	increased tidal volume		IEA		N	RGD:5509061	20260402	MGI			
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884307
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:10884307
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0009974	decreased cerebral cortex pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0010012	ectopic cerebral cortex pyramidal cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:17682066
1551967	St8sia4	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	gene	MP:0014551	impaired neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:17682066
1551968	Max	Max protein	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640271
1551968	Max	Max protein	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640271
1551968	Max	Max protein	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640271
1551968	Max	Max protein	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640271
1551968	Max	Max protein	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640271
1551968	Max	Max protein	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640271
1551968	Max	Max protein	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640271
1551968	Max	Max protein	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10640271
1551969	Grm4	glutamate receptor, metabotropic 4	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8815915
1551969	Grm4	glutamate receptor, metabotropic 4	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8815915
1551969	Grm4	glutamate receptor, metabotropic 4	gene	MP:0002922	decreased post-tetanic potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8815915
1551969	Grm4	glutamate receptor, metabotropic 4	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20141003	MGI			
1551970	Krt27	keratin 27	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20210520	MGI			
1551970	Krt27	keratin 27	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1551970	Krt27	keratin 27	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1551970	Krt27	keratin 27	gene	MP:0000397	abnormal guard hair morphology		IEA		N	RGD:5509061	20150730	MGI			
1551970	Krt27	keratin 27	gene	MP:0000402	abnormal zigzag hair morphology		IEA		N	RGD:5509061	20150730	MGI			
1551970	Krt27	keratin 27	gene	MP:0000410	waved hair		IEA		N	RGD:5509061	20111116	MGI			
1551970	Krt27	keratin 27	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1551970	Krt27	keratin 27	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1551970	Krt27	keratin 27	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1551970	Krt27	keratin 27	gene	MP:0001274	curly vibrissae		IEA		N	RGD:5509061	20150730	MGI			
1551970	Krt27	keratin 27	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1551970	Krt27	keratin 27	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1551970	Krt27	keratin 27	gene	MP:0002073	abnormal hair growth		IEA		N	RGD:5509061	20111116	MGI			
1551970	Krt27	keratin 27	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20111116	MGI			
1551970	Krt27	keratin 27	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1551970	Krt27	keratin 27	gene	MP:0003809	abnormal hair shaft morphology		IEA		N	RGD:5509061	20111116	MGI			
1551970	Krt27	keratin 27	gene	MP:0010179	rough coat		IEA		N	RGD:5509061	20150730	MGI			
1551972	Nek6	NIMA (never in mitosis gene a)-related expressed kinase 6	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141225	MGI			PMID:24763737
1551972	Nek6	NIMA (never in mitosis gene a)-related expressed kinase 6	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1551972	Nek6	NIMA (never in mitosis gene a)-related expressed kinase 6	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141225	MGI			PMID:24763737
1551972	Nek6	NIMA (never in mitosis gene a)-related expressed kinase 6	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141225	MGI			PMID:24763737
1551972	Nek6	NIMA (never in mitosis gene a)-related expressed kinase 6	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141225	MGI			PMID:24763737
1551972	Nek6	NIMA (never in mitosis gene a)-related expressed kinase 6	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141225	MGI			PMID:24763737
1551972	Nek6	NIMA (never in mitosis gene a)-related expressed kinase 6	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141225	MGI			PMID:24763737
1551972	Nek6	NIMA (never in mitosis gene a)-related expressed kinase 6	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:24763737
1551973	Odc1	ornithine decarboxylase, structural 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:11533243
1551973	Odc1	ornithine decarboxylase, structural 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1551973	Odc1	ornithine decarboxylase, structural 1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11533243
1551973	Odc1	ornithine decarboxylase, structural 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11533243
1551973	Odc1	ornithine decarboxylase, structural 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551973	Odc1	ornithine decarboxylase, structural 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1551974	Fzd5	frizzled class receptor 5	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509025
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509025
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509025
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509025
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509025
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092808
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092808
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092808
1551974	Fzd5	frizzled class receptor 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092808
1551974	Fzd5	frizzled class receptor 5	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20191219	MGI			PMID:18489003
1551974	Fzd5	frizzled class receptor 5	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092808
1551974	Fzd5	frizzled class receptor 5	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:18489003
1551974	Fzd5	frizzled class receptor 5	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20191219	MGI			PMID:18489003
1551974	Fzd5	frizzled class receptor 5	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20191219	MGI			PMID:18489003
1551974	Fzd5	frizzled class receptor 5	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0006200	vitreous body deposition		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0008509	disorganized retina ganglion layer		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092808
1551974	Fzd5	frizzled class receptor 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092808
1551974	Fzd5	frizzled class receptor 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18509025
1551974	Fzd5	frizzled class receptor 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551974	Fzd5	frizzled class receptor 5	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0011964	increased total retina thickness		IAGP		N	RGD:5509061	20191219	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0014077	ectopic Paneth cells		IAGP		N	RGD:5509061	20160310	MGI			PMID:15778706
1551974	Fzd5	frizzled class receptor 5	gene	MP:0021107	retina fold		IAGP		N	RGD:5509061	20220331	MGI			PMID:18791178
1551974	Fzd5	frizzled class receptor 5	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20191219	MGI			PMID:18489003
1551975	Ddx52	DExD box helicase 52	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1551975	Ddx52	DExD box helicase 52	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1551975	Ddx52	DExD box helicase 52	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20160804	MGI			
1551979	Coq4	coenzyme Q4	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1551979	Coq4	coenzyme Q4	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1551979	Coq4	coenzyme Q4	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1551979	Coq4	coenzyme Q4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1551979	Coq4	coenzyme Q4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551980	Pskh1	protein serine kinase H1	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1551980	Pskh1	protein serine kinase H1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1551980	Pskh1	protein serine kinase H1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1551980	Pskh1	protein serine kinase H1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1551980	Pskh1	protein serine kinase H1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1551980	Pskh1	protein serine kinase H1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1551980	Pskh1	protein serine kinase H1	gene	MP:0010853	abnormal lung position or orientation		IEA		N	RGD:5509061	20141003	MGI			
1551980	Pskh1	protein serine kinase H1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551980	Pskh1	protein serine kinase H1	gene	MP:0011252	situs inversus totalis		IEA		N	RGD:5509061	20141003	MGI			
1551980	Pskh1	protein serine kinase H1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1551984	Mtarc2	mitochondrial amidoxime reducing component 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20240509	MGI			PMID:38437227
1551984	Mtarc2	mitochondrial amidoxime reducing component 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:38437227
1551984	Mtarc2	mitochondrial amidoxime reducing component 2	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20240509	MGI			PMID:38437227
1551985	Eml3	echinoderm microtubule associated protein like 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20241121	MGI			
1551985	Eml3	echinoderm microtubule associated protein like 3	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1551985	Eml3	echinoderm microtubule associated protein like 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1551985	Eml3	echinoderm microtubule associated protein like 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1551985	Eml3	echinoderm microtubule associated protein like 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1551985	Eml3	echinoderm microtubule associated protein like 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1551987	Ints12	integrator complex subunit 12	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1551987	Ints12	integrator complex subunit 12	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1551987	Ints12	integrator complex subunit 12	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1551987	Ints12	integrator complex subunit 12	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20160804	MGI			
1551987	Ints12	integrator complex subunit 12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17318223
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:7698643
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:17318223
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20240523	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20240523	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001214	skin hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:7698643
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20240523	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17318223
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:15489954
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:17184942
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:15489954
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:15494543
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:9922314
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20240523	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15489954
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:15554929
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:9922314
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:17184942
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11097843
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15699164
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20200310	MGI			PMID:15699164
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15699164
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20200310	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17318223
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20201231	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21270334
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20200310	MGI			PMID:17318223
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20200310	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:15494543
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20200310	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0004925	decreased susceptibility to noise-induced hearing loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:17184942
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20260402	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:15554929
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20201022	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0005527	increased renal glomerular filtration rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:15494543
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15494543
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20210128	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15489954
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15489954
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200310	MGI			PMID:15489954
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:10051636
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:15699164
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20210128	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17318223
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0011372	decreased renal tubule apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15494543
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0011452	decreased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20200310	MGI			PMID:7698643
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20200310	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:9207086
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20200310	MGI			PMID:17318223
1551988	Parp1	poly (ADP-ribose) polymerase family, member 1	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20230824	MGI			PMID:17318223
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000126	brittle teeth		IAGP		N	RGD:5509061	20180125	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000132	thickened long bone epiphysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0003671	abnormal eyelid aperture		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20220915	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:18985159
1551989	Slc39a13	solute carrier family 39 (metal ion transporter), member 13	gene	MP:0030494	abnormal molar root morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:18985159
1551991	Cnmd	chondromodulin	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509461
1551991	Cnmd	chondromodulin	gene	MP:0000064	failure of bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509461
1551991	Cnmd	chondromodulin	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509461
1551991	Cnmd	chondromodulin	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509461
1551991	Cnmd	chondromodulin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12192060
1551991	Cnmd	chondromodulin	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509461
1551991	Cnmd	chondromodulin	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509461
1551991	Cnmd	chondromodulin	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:12509461
1551991	Cnmd	chondromodulin	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20220922	MGI			PMID:12509461
1551991	Cnmd	chondromodulin	gene	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:12509461
1551993	Dtl	denticleless E3 ubiquitin protein ligase	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1551993	Dtl	denticleless E3 ubiquitin protein ligase	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17107960
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0001411	spinning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20200709	MGI			PMID:24648452
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208842
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20200709	MGI			PMID:24648452
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20200709	MGI			PMID:24648452
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20200709	MGI			PMID:24648452
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20200709	MGI			PMID:24648452
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382139
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20693420
1551994	Usp18	ubiquitin specific peptidase 18	gene	MP:0020950	decreased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200709	MGI			PMID:24648452
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817122
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817122
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0003442	decreased circulating glycerol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817122
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0004772	abnormal bile secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20830789
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817122
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817122
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817122
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20830789
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20830789
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20830789
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0010967	increased compact bone area		IAGP		N	RGD:5509061	20141003	MGI			PMID:20817122
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0014480	increased feces cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:20817122
1551996	P2ry13	purinergic receptor P2Y, G-protein coupled 13	gene	MP:0031683	abnormal cholesterol transport		IAGP		N	RGD:5509061	20251023	MGI			PMID:20830789
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:1759682
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:2164218
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16904100
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16904100
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:1759682
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:2164218
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1759682
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1759682
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2164218
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:1759682
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:2164218
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1551997	Fndc3a	fibronectin type III domain containing 3A	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:2164218
1551998	Mpp2	membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2)	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
1551998	Mpp2	membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2)	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1551998	Mpp2	membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2)	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1551998	Mpp2	membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2)	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20241121	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20231207	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20231207	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20231207	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20231207	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0003394	increased cardiac output		IEA		N	RGD:5509061	20240523	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20240523	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20240523	MGI			
1552001	Wdr27	WD repeat domain 27	gene	MP:0010574	dilated aorta		IEA		N	RGD:5509061	20240523	MGI			
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20250102	MGI			PMID:33913576
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250102	MGI			PMID:33913576
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201231	MGI			
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20250102	MGI			PMID:33913576
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20250102	MGI			PMID:33913576
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20250102	MGI			PMID:33913576
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20250102	MGI			PMID:33913576
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1552002	Ppp2r1b	protein phosphatase 2, regulatory subunit A, beta	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20250102	MGI			PMID:33913576
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305648
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18971423
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909628
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909628
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20191003	MGI			PMID:30675063
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653504
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20191003	MGI			PMID:30675063
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23334413
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809547
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18843253
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21060874
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002759	abnormal caudal vertebrae morphology		IEA		N	RGD:5509061	20220811	MGI			
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210128	MGI			
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305648
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20305648
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909628
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569158
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18843253
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20210211	MGI			PMID:32755573
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18843253
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21060874
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809547
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653504
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569158
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12600915
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005546	choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005546	choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909628
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005549	retina pigment epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0006051	brainstem hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0006187	retina deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0006187	retina deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909628
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653504
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23334413
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17909628
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20210211	MGI			PMID:32755573
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008837	increased transforming growth factor beta level		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12600915
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20211202	MGI			PMID:32923620
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200827	MGI			PMID:31771656
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653504
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0010016	variable depigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652758
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20210211	MGI			PMID:32755573
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732273
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20210211	MGI			PMID:32755573
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29669747
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:23637822
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0031509	decreased vascular smooth muscle cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:16809547
1552004	Cx3cr1	C-X3-C motif chemokine receptor 1	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:23637822
1552006	Dag1	dystroglycan 1	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21388311
1552006	Dag1	dystroglycan 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20240801	MGI			PMID:38616731
1552006	Dag1	dystroglycan 1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579745
1552006	Dag1	dystroglycan 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1552006	Dag1	dystroglycan 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21388311
1552006	Dag1	dystroglycan 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240801	MGI			PMID:38616731
1552006	Dag1	dystroglycan 1	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19846701
1552006	Dag1	dystroglycan 1	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19846701
1552006	Dag1	dystroglycan 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21388311
1552006	Dag1	dystroglycan 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175728
1552006	Dag1	dystroglycan 1	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175728
1552006	Dag1	dystroglycan 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175728
1552006	Dag1	dystroglycan 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20240801	MGI			PMID:38616731
1552006	Dag1	dystroglycan 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175728
1552006	Dag1	dystroglycan 1	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19846701
1552006	Dag1	dystroglycan 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175728
1552006	Dag1	dystroglycan 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175728
1552006	Dag1	dystroglycan 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38616731
1552006	Dag1	dystroglycan 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810924
1552006	Dag1	dystroglycan 1	gene	MP:0002546	mydriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19846701
1552006	Dag1	dystroglycan 1	gene	MP:0002583	absent extraembryonic ectoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175728
1552006	Dag1	dystroglycan 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797173
1552006	Dag1	dystroglycan 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1552006	Dag1	dystroglycan 1	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797173
1552006	Dag1	dystroglycan 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38616731
1552006	Dag1	dystroglycan 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797173
1552006	Dag1	dystroglycan 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579745
1552006	Dag1	dystroglycan 1	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175728
1552006	Dag1	dystroglycan 1	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20240801	MGI			PMID:38616731
1552006	Dag1	dystroglycan 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19846701
1552006	Dag1	dystroglycan 1	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0004262	abnormal physical strength		IAGP		N	RGD:5509061	20240801	MGI			PMID:38616731
1552006	Dag1	dystroglycan 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1552006	Dag1	dystroglycan 1	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19797173
1552006	Dag1	dystroglycan 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810924
1552006	Dag1	dystroglycan 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579745
1552006	Dag1	dystroglycan 1	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579745
1552006	Dag1	dystroglycan 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579745
1552006	Dag1	dystroglycan 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0008285	abnormal hippocampus granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579745
1552006	Dag1	dystroglycan 1	gene	MP:0009027	abnormal subarachnoid space morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:19846701
1552006	Dag1	dystroglycan 1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:21388311
1552006	Dag1	dystroglycan 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810924
1552006	Dag1	dystroglycan 1	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1552006	Dag1	dystroglycan 1	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1552006	Dag1	dystroglycan 1	gene	MP:0009695	abnormal spinal cord ventral commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23217742
1552006	Dag1	dystroglycan 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:21388311
1552006	Dag1	dystroglycan 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810924
1552006	Dag1	dystroglycan 1	gene	MP:0010238	increased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12230980
1552006	Dag1	dystroglycan 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19846701
1552006	Dag1	dystroglycan 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240801	MGI			PMID:38616731
1552006	Dag1	dystroglycan 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9175728
1552006	Dag1	dystroglycan 1	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20150430	MGI			PMID:19846701
1552006	Dag1	dystroglycan 1	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:12140559
1552006	Dag1	dystroglycan 1	gene	MP:0020391	radial glial endfoot detachment		IAGP		N	RGD:5509061	20161117	MGI			PMID:23217742
1552006	Dag1	dystroglycan 1	gene	MP:0021155	abnormal heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:19797173
1552007	Zfp184	zinc finger protein 184 (Kruppel-like)	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200310	MGI			
1552008	Gip	gastric inhibitory polypeptide	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:31977316
1552008	Gip	gastric inhibitory polypeptide	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20241121	MGI			PMID:31977316
1552008	Gip	gastric inhibitory polypeptide	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1552008	Gip	gastric inhibitory polypeptide	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20241121	MGI			PMID:31977316
1552008	Gip	gastric inhibitory polypeptide	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20241121	MGI			PMID:31977316
1552008	Gip	gastric inhibitory polypeptide	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20241121	MGI			PMID:31977316
1552008	Gip	gastric inhibitory polypeptide	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20241121	MGI			PMID:31977316
1552008	Gip	gastric inhibitory polypeptide	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20241121	MGI			PMID:31977316
1552009	Bcl2l1	BCL2-like 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17382885
1552009	Bcl2l1	BCL2-like 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15905539
1552009	Bcl2l1	BCL2-like 1	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:18566418
1552009	Bcl2l1	BCL2-like 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:11150333
1552009	Bcl2l1	BCL2-like 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11150333
1552009	Bcl2l1	BCL2-like 1	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16033881
1552009	Bcl2l1	BCL2-like 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:16033881
1552009	Bcl2l1	BCL2-like 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16033881
1552009	Bcl2l1	BCL2-like 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093873
1552009	Bcl2l1	BCL2-like 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17382885
1552009	Bcl2l1	BCL2-like 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11150333
1552009	Bcl2l1	BCL2-like 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9096145
1552009	Bcl2l1	BCL2-like 1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9096145
1552009	Bcl2l1	BCL2-like 1	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16033881
1552009	Bcl2l1	BCL2-like 1	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:18566418
1552009	Bcl2l1	BCL2-like 1	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17382885
1552009	Bcl2l1	BCL2-like 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093873
1552009	Bcl2l1	BCL2-like 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15905539
1552009	Bcl2l1	BCL2-like 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18566418
1552009	Bcl2l1	BCL2-like 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093873
1552009	Bcl2l1	BCL2-like 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17382885
1552009	Bcl2l1	BCL2-like 1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17382885
1552009	Bcl2l1	BCL2-like 1	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16033881
1552009	Bcl2l1	BCL2-like 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11150333
1552009	Bcl2l1	BCL2-like 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9096145
1552009	Bcl2l1	BCL2-like 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11150333
1552009	Bcl2l1	BCL2-like 1	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093873
1552009	Bcl2l1	BCL2-like 1	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093873
1552009	Bcl2l1	BCL2-like 1	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17382885
1552009	Bcl2l1	BCL2-like 1	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12665473
1552009	Bcl2l1	BCL2-like 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20929728
1552009	Bcl2l1	BCL2-like 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:12093873
1552009	Bcl2l1	BCL2-like 1	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19209227
1552009	Bcl2l1	BCL2-like 1	gene	MP:0009580	increased keratinocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12665473
1552009	Bcl2l1	BCL2-like 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9096145
1552009	Bcl2l1	BCL2-like 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17382885
1552009	Bcl2l1	BCL2-like 1	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:10894153
1552009	Bcl2l1	BCL2-like 1	gene	MP:0020543	decreased substantia nigra size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16033881
1552009	Bcl2l1	BCL2-like 1	gene	MP:0030578	decreased keratinocyte adhesion		IAGP		N	RGD:5509061	20200310	MGI			PMID:12665473
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20241121	MGI			
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20241121	MGI			
1552011	Pitpnc1	phosphatidylinositol transfer protein, cytoplasmic 1	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20230601	MGI			
1552013	Smyd2	SET and MYND domain containing 2	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1552013	Smyd2	SET and MYND domain containing 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1552014	Prrg4	proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane)	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1552014	Prrg4	proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane)	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1552014	Prrg4	proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane)	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230601	MGI			
1552014	Prrg4	proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane)	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1552014	Prrg4	proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane)	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1552014	Prrg4	proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane)	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1552015	Kcnip4	Kv channel interacting protein 4	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0009658	increased placenta apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0010038	abnormal placenta physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1552019	Ssr3	signal sequence receptor, gamma	gene	MP:0011521	decreased placental labyrinth size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246656
1552021	Dohh	deoxyhypusine hydroxylase/monooxygenase	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24832488
1552021	Dohh	deoxyhypusine hydroxylase/monooxygenase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:26037925
1552021	Dohh	deoxyhypusine hydroxylase/monooxygenase	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26037925
1552021	Dohh	deoxyhypusine hydroxylase/monooxygenase	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26037925
1552021	Dohh	deoxyhypusine hydroxylase/monooxygenase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:26037925
1552021	Dohh	deoxyhypusine hydroxylase/monooxygenase	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26037925
1552021	Dohh	deoxyhypusine hydroxylase/monooxygenase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20200310	MGI			PMID:26037925
1552021	Dohh	deoxyhypusine hydroxylase/monooxygenase	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26037925
1552021	Dohh	deoxyhypusine hydroxylase/monooxygenase	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:24832488
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210520	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210520	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20210520	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20210520	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1552022	Disp3	dispatched RND transporter family member 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210128	MGI			
1552024	Taar5	trace amine-associated receptor 5	gene	MP:0001983	abnormal olfactory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837392
1552025	Syt9	synaptotagmin IX	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1552025	Syt9	synaptotagmin IX	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20210826	MGI			
1552025	Syt9	synaptotagmin IX	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1552027	Ep300	E1A binding protein p300	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0000296	absent trabeculae carneae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237459
1552027	Ep300	E1A binding protein p300	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428436
1552027	Ep300	E1A binding protein p300	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12384703
1552027	Ep300	E1A binding protein p300	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428436
1552027	Ep300	E1A binding protein p300	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517256
1552027	Ep300	E1A binding protein p300	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12384703
1552027	Ep300	E1A binding protein p300	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237459
1552027	Ep300	E1A binding protein p300	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12384703
1552027	Ep300	E1A binding protein p300	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517256
1552027	Ep300	E1A binding protein p300	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237459
1552027	Ep300	E1A binding protein p300	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517256
1552027	Ep300	E1A binding protein p300	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237459
1552027	Ep300	E1A binding protein p300	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141225	MGI			
1552027	Ep300	E1A binding protein p300	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12384703
1552027	Ep300	E1A binding protein p300	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12384703
1552027	Ep300	E1A binding protein p300	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12384703
1552027	Ep300	E1A binding protein p300	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517256
1552027	Ep300	E1A binding protein p300	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428436
1552027	Ep300	E1A binding protein p300	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428436
1552027	Ep300	E1A binding protein p300	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428436
1552027	Ep300	E1A binding protein p300	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12384703
1552027	Ep300	E1A binding protein p300	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237459
1552027	Ep300	E1A binding protein p300	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428436
1552027	Ep300	E1A binding protein p300	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16428436
1552027	Ep300	E1A binding protein p300	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0008188	abnormal transitional stage B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0008240	abnormal spleen marginal zone macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12384703
1552027	Ep300	E1A binding protein p300	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18684867
1552027	Ep300	E1A binding protein p300	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517256
1552027	Ep300	E1A binding protein p300	gene	MP:0010138	arteritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0010500	myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0010592	abnormal atrioventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12384703
1552027	Ep300	E1A binding protein p300	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237459
1552027	Ep300	E1A binding protein p300	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517256
1552027	Ep300	E1A binding protein p300	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517256
1552027	Ep300	E1A binding protein p300	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237459
1552027	Ep300	E1A binding protein p300	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517256
1552027	Ep300	E1A binding protein p300	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590171
1552027	Ep300	E1A binding protein p300	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517255
1552027	Ep300	E1A binding protein p300	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:17513743
1552027	Ep300	E1A binding protein p300	gene	MP:0031590	abnormal epicardium development		IAGP		N	RGD:5509061	20240229	MGI			PMID:14517255
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20210617	MGI			PMID:31883536
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20210617	MGI			PMID:31883536
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20210617	MGI			PMID:31883536
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20210617	MGI			PMID:31883536
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20210617	MGI			PMID:31883536
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20210617	MGI			PMID:31883536
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0013772	increased effector memory T-helper cell number		IAGP		N	RGD:5509061	20210722	MGI			PMID:28333124
1552028	Bcap31	B cell receptor associated protein 31	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20210617	MGI			PMID:31883536
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371805
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371805
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231455
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231455
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231455
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231455
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231455
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371805
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231455
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371805
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371805
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371805
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371805
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0003996	clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231455
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20231455
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1552030	Sptbn2	spectrin beta, non-erythrocytic 2	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:20371805
1552032	Pfkfb4	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20230601	MGI			
1552032	Pfkfb4	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1552032	Pfkfb4	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1552035	Trmt61a	tRNA methyltransferase 61A	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1552035	Trmt61a	tRNA methyltransferase 61A	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1552035	Trmt61a	tRNA methyltransferase 61A	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1552035	Trmt61a	tRNA methyltransferase 61A	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1552035	Trmt61a	tRNA methyltransferase 61A	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1552035	Trmt61a	tRNA methyltransferase 61A	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1552035	Trmt61a	tRNA methyltransferase 61A	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1552035	Trmt61a	tRNA methyltransferase 61A	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:36138184
1552037	Capn11	calpain 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1552037	Capn11	calpain 11	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1552038	Prss59	protease, serine 59	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20210415	MGI			PMID:32020604
1552038	Prss59	protease, serine 59	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210415	MGI			PMID:32020604
1552038	Prss59	protease, serine 59	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20210415	MGI			PMID:32020604
1552040	Agbl2	ATP/GTP binding protein-like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:25103237
1552041	Tcf21	transcription factor 21	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573622
1552041	Tcf21	transcription factor 21	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573622
1552041	Tcf21	transcription factor 21	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289436
1552041	Tcf21	transcription factor 21	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289436
1552041	Tcf21	transcription factor 21	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0001184	absent pulmonary alveoli		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0001184	absent pulmonary alveoli		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0001939	secondary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289436
1552041	Tcf21	transcription factor 21	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21432986
1552041	Tcf21	transcription factor 21	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573622
1552041	Tcf21	transcription factor 21	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289436
1552041	Tcf21	transcription factor 21	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0003605	fused kidneys		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0004234	abnormal masticatory muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0004236	absent masseter muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0004237	abnormal pterygoid muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0004238	absent pterygoid muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0004240	absent temporalis muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573622
1552041	Tcf21	transcription factor 21	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0005652	sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289436
1552041	Tcf21	transcription factor 21	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0006419	disorganized testis cords		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289436
1552041	Tcf21	transcription factor 21	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0008727	increased heart right atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573622
1552041	Tcf21	transcription factor 21	gene	MP:0009323	abnormal spleen development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20150205	MGI			PMID:24904088
1552041	Tcf21	transcription factor 21	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0010812	absent type II pneumocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0010856	dilated respiratory conducting tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0010902	abnormal pulmonary alveolar sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0010911	abnormal pulmonary acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0010976	small lung lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0010981	abnormal branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0010985	abnormal kidney mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0011028	impaired branching involved in bronchus morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0011038	impaired branching involved in alveolar sac morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12493912
1552041	Tcf21	transcription factor 21	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21432986
1552041	Tcf21	transcription factor 21	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1552041	Tcf21	transcription factor 21	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0011298	ureter hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792366
1552041	Tcf21	transcription factor 21	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0011321	abnormal peritubular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0011351	absent proximal convoluted tubule brush border		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0011363	renal glomerulus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10944221
1552041	Tcf21	transcription factor 21	gene	MP:0011727	ectopic ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289436
1552041	Tcf21	transcription factor 21	gene	MP:0011760	abnormal ureteric bud tip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10572052
1552041	Tcf21	transcription factor 21	gene	MP:0012515	abnormal heart apex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573622
1552041	Tcf21	transcription factor 21	gene	MP:0020491	abnormal ovary topology		IAGP		N	RGD:5509061	20171026	MGI			PMID:15289436
1552044	Lysmd3	LysM, putative peptidoglycan-binding, domain containing 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20181220	MGI			PMID:29496999
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20181227	MGI			
1552045	Ica1l	islet cell autoantigen 1-like	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:26306493
1552046	Dcakd	dephospho-CoA kinase domain containing	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1552046	Dcakd	dephospho-CoA kinase domain containing	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1552047	Cops4	COP9 signalosome subunit 4	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1552047	Cops4	COP9 signalosome subunit 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20141003	MGI			
1552047	Cops4	COP9 signalosome subunit 4	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20141003	MGI			
1552047	Cops4	COP9 signalosome subunit 4	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1552047	Cops4	COP9 signalosome subunit 4	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1552050	Tchhl1	trichohyalin-like 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20221215	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20111116	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0000607	abnormal hepatocyte morphology		IEA		N	RGD:5509061	20111116	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20231207	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0001655	multifocal hepatic necrosis		IEA		N	RGD:5509061	20111116	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0002981	increased liver weight		IEA		N	RGD:5509061	20111116	MGI			
1552051	Clca2	chloride channel accessory 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230119	MGI			
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17549259
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18463233
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:19319191
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12068289
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12032136
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12068289
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12068289
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12860835
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12860835
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12068289
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18463233
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17549259
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:18431508
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18463233
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16326714
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19319191
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:18431508
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20200310	MGI			PMID:25590242
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19319191
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003948	abnormal gas homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17549259
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:12032136
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:12138120
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20200310	MGI			PMID:24531262
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:24531262
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12032136
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16326714
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12032136
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12068289
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17693256
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24531262
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005413	vascular restenosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12138120
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19319191
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:12860835
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:12860835
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20200310	MGI			PMID:18431508
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0008907	decreased total fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15907819
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19319191
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20200310	MGI			PMID:24531262
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0011016	increased core body temperature		IAGP		N	RGD:5509061	20200310	MGI			PMID:24531262
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19319191
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0012575	increased noradrenaline level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0014174	decreased fatty acid beta-oxidation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12151381
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0014752	abnormal tumor cell proliferation		IAGP		N	RGD:5509061	20250925	MGI			PMID:19319191
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0014755	increased tumor cell proliferation		IAGP		N	RGD:5509061	20250925	MGI			PMID:19319191
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0020318	increased vascular endothelial cell adhesion		IAGP		N	RGD:5509061	20200310	MGI			PMID:17549259
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24531262
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0030770	increased urine adrenaline level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17549259
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17693256
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19319191
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0030984	increased circulating osteocalcin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23684624
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:16595853
1552054	Adipoq	adiponectin, C1Q and collagen domain containing	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15907819
1552056	Lipm	lipase family member M	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20221215	MGI			
1552056	Lipm	lipase family member M	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20200310	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20200310	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:19521792
1552058	Ift172	intraflagellar transport 172	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:19521792
1552058	Ift172	intraflagellar transport 172	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1552058	Ift172	intraflagellar transport 172	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1552058	Ift172	intraflagellar transport 172	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:19666503
1552058	Ift172	intraflagellar transport 172	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1552058	Ift172	intraflagellar transport 172	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:16061793
1552058	Ift172	intraflagellar transport 172	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:16061793
1552058	Ift172	intraflagellar transport 172	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1552058	Ift172	intraflagellar transport 172	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:29659833
1552058	Ift172	intraflagellar transport 172	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19521792
1552058	Ift172	intraflagellar transport 172	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20200310	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1552058	Ift172	intraflagellar transport 172	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20200310	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:20511334
1552058	Ift172	intraflagellar transport 172	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20200402	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19521792
1552058	Ift172	intraflagellar transport 172	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19666503
1552058	Ift172	intraflagellar transport 172	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20200310	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0003130	anal atresia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20200310	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29659833
1552058	Ift172	intraflagellar transport 172	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1552058	Ift172	intraflagellar transport 172	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1552058	Ift172	intraflagellar transport 172	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:16061793
1552058	Ift172	intraflagellar transport 172	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:29659833
1552058	Ift172	intraflagellar transport 172	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:29659833
1552058	Ift172	intraflagellar transport 172	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20200310	MGI			PMID:29659833
1552058	Ift172	intraflagellar transport 172	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200310	MGI			PMID:29659833
1552058	Ift172	intraflagellar transport 172	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20511334
1552058	Ift172	intraflagellar transport 172	gene	MP:0008772	increased heart ventricle size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20511334
1552058	Ift172	intraflagellar transport 172	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0009377	ectopic manchette		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:20511334
1552058	Ift172	intraflagellar transport 172	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201022	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:20511334
1552058	Ift172	intraflagellar transport 172	gene	MP:0010881	esophagus hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0010884	esophagus stenosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19521792
1552058	Ift172	intraflagellar transport 172	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:14603322
1552058	Ift172	intraflagellar transport 172	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15755804
1552058	Ift172	intraflagellar transport 172	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16061793
1552058	Ift172	intraflagellar transport 172	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18930042
1552058	Ift172	intraflagellar transport 172	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20200310	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200310	MGI			PMID:29659833
1552058	Ift172	intraflagellar transport 172	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200310	MGI			PMID:29659833
1552058	Ift172	intraflagellar transport 172	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:18488998
1552058	Ift172	intraflagellar transport 172	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:21653639
1552058	Ift172	intraflagellar transport 172	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552058	Ift172	intraflagellar transport 172	gene	MP:0014684	impaired spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29659833
1552058	Ift172	intraflagellar transport 172	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:31958312
1552058	Ift172	intraflagellar transport 172	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20220428	MGI			PMID:31958312
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0014684	impaired spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20230727	MGI			PMID:36306217
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552060	Tssk3	testis-specific serine kinase 3	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:34623009
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18843253
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165355
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22577176
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275892
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362535
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351623
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362535
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362535
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843684
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20220811	MGI			
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751350
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001655	multifocal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362535
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362535
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843684
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9366570
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351623
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986513
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351623
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12504109
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10438957
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362535
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17257744
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18843253
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21060874
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986513
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002570	alcohol aversion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002620	abnormal monocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17364026
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10438957
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751350
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20211021	MGI			PMID:31813573
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843684
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11591787
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21458307
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351623
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17257744
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003546	decreased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275892
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11591787
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351623
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12504109
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351623
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18843253
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641140
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22190646
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362535
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9366570
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732872
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22577176
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751350
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751350
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20231207	MGI			
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18843253
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015448
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21060874
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12065319
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0004983	abnormal osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9362535
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843684
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22577176
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843684
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11591787
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015448
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005098	abnormal optic choroid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20211021	MGI			PMID:31813573
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21779871
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12504109
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986513
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986513
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18165355
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732872
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005362	abnormal Langerhans cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16444257
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005546	choroidal neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18843253
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10438957
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20231207	MGI			
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21779871
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0006187	retina deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0006238	abnormal choriocapillaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0006315	abnormal urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986513
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843684
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843684
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10843684
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20483766
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751350
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751350
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015448
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11591787
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9366570
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9366570
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015448
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641140
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9366570
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14566334
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751350
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23986513
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11015448
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275892
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0009878	decreased susceptibility to bone fracture		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0010119	abnormal bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0010740	abnormal dendritic cell chemotaxis		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9366570
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19330010
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16105698
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0013648	increased CD11b-high dendritic cell number		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0013649	decreased CD11b-high dendritic cell number		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:19357362
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:19079579
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200514	MGI			PMID:11591787
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:21779871
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:11591787
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0031054	bronchiolitis		IAGP		N	RGD:5509061	20200709	MGI			PMID:19079579
1552061	Ccr2	C-C motif chemokine receptor 2	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:14566334
1552063	Kif15	kinesin family member 15	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36934586
1552063	Kif15	kinesin family member 15	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20231109	MGI			PMID:36934586
1552063	Kif15	kinesin family member 15	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:36934586
1552063	Kif15	kinesin family member 15	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:36934586
1552063	Kif15	kinesin family member 15	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20231109	MGI			PMID:36934586
1552063	Kif15	kinesin family member 15	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20231109	MGI			PMID:36934586
1552063	Kif15	kinesin family member 15	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20231109	MGI			PMID:36934586
1552066	Tmtc2	transmembrane and tetratricopeptide repeat containing 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1552066	Tmtc2	transmembrane and tetratricopeptide repeat containing 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1552066	Tmtc2	transmembrane and tetratricopeptide repeat containing 2	gene	MP:0009453	enhanced contextual conditioning behavior		IEA		N	RGD:5509061	20230601	MGI			
1552066	Tmtc2	transmembrane and tetratricopeptide repeat containing 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20241121	MGI			
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552067	Spink2	serine peptidase inhibitor, Kazal type 2	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21705336
1552068	Kcne4	potassium voltage-gated channel, Isk-related subfamily, gene 4	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20211104	MGI			PMID:26399785
1552068	Kcne4	potassium voltage-gated channel, Isk-related subfamily, gene 4	gene	MP:0020345	abnormal myocardial fiber currents		IAGP		N	RGD:5509061	20211104	MGI			PMID:26399785
1552068	Kcne4	potassium voltage-gated channel, Isk-related subfamily, gene 4	gene	MP:0020418	increased cardiac muscle relaxation		IAGP		N	RGD:5509061	20211104	MGI			PMID:26399785
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879845
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879845
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879845
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267101
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267101
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267101
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001181	absent lungs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267101
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879845
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879845
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267101
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002691	small stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003655	absent pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267101
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003703	abnormal vestibulocochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003936	abnormal reproductive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267101
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006292	abnormal nasal placode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006339	abnormal third pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006339	abnormal third pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006340	abnormal fourth pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006347	abnormal sixth pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267101
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267101
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009705	abnormal midgut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009806	abnormal otic vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009806	abnormal otic vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009806	abnormal otic vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0010356	abnormal second pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0010643	absent fourth pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0010643	absent fourth pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0010644	absent sixth pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0010707	decreased ventral retina size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0010907	absent lung buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0011026	impaired branching involved in trachea morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0011233	abnormal vitamin A metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0012247	absent cornea		IAGP		N	RGD:5509061	20171019	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0012270	cardiac edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0013164	abnormal forelimb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0013166	small forelimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0013166	small forelimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930923
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0013817	absent nasal cavity		IAGP		N	RGD:5509061	20171019	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:17473173
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0020350	fused pharyngeal arches		IAGP		N	RGD:5509061	20160915	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0020350	fused pharyngeal arches		IAGP		N	RGD:5509061	20160915	MGI			PMID:22319578
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0030250	frontonasal prominence hypoplasia		IAGP		N	RGD:5509061	20171019	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0030334	absent sixth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0030335	absent third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:21305688
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221124	MGI			PMID:31300413
1552069	Rdh10	retinol dehydrogenase 10 (all-trans)	gene	MP:0031464	abnormal spontaneous fetal mouth movement		IAGP		N	RGD:5509061	20230302	MGI			PMID:31300413
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:33536340
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20211209	MGI			PMID:32976492
1552071	Tbc1d21	TBC1 domain family, member 21	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:32976492
1552078	Kif2b	kinesin family member 2B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879343
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879343
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879343
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879343
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879343
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0002824	abnormal chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879343
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879343
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1879343
1552080	Vps26a	VPS26 retromer complex component A	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16214895
1552084	Mapkapk3	mitogen-activated protein kinase-activated protein kinase 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1552084	Mapkapk3	mitogen-activated protein kinase-activated protein kinase 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1552084	Mapkapk3	mitogen-activated protein kinase-activated protein kinase 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1552084	Mapkapk3	mitogen-activated protein kinase-activated protein kinase 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1552084	Mapkapk3	mitogen-activated protein kinase-activated protein kinase 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1552084	Mapkapk3	mitogen-activated protein kinase-activated protein kinase 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1552084	Mapkapk3	mitogen-activated protein kinase-activated protein kinase 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1552084	Mapkapk3	mitogen-activated protein kinase-activated protein kinase 3	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:17030606
1552087	Zfp219	zinc finger protein 219	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1552087	Zfp219	zinc finger protein 219	gene	MP:0001759	increased urine glucose level		IEA		N	RGD:5509061	20211021	MGI			
1552087	Zfp219	zinc finger protein 219	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20210520	MGI			
1552087	Zfp219	zinc finger protein 219	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1552092	Zbtb12	zinc finger and BTB domain containing 12	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210826	MGI			
1552092	Zbtb12	zinc finger and BTB domain containing 12	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1552092	Zbtb12	zinc finger and BTB domain containing 12	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1552092	Zbtb12	zinc finger and BTB domain containing 12	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1552092	Zbtb12	zinc finger and BTB domain containing 12	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20250508	MGI			
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0004182	abnormal spermiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0009839	multiflagellated sperm		IAGP		N	RGD:5509061	20220630	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:12556490
1552095	Gmcl1	germ cell-less, spermatogenesis associated 1	gene	MP:0031408	multi-headed sperm		IAGP		N	RGD:5509061	20220630	MGI			PMID:12556490
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507984
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507985
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16507985
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0012134	absent umbilical cord		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0012301	absent umbilical cord blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:18612384
1552096	Tnks2	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:18612384
1552098	Lrrc49	leucine rich repeat containing 49	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20200310	MGI			
1552098	Lrrc49	leucine rich repeat containing 49	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552098	Lrrc49	leucine rich repeat containing 49	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20210128	MGI			
1552099	Baz2a	bromodomain adjacent to zinc finger domain, 2A	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1552099	Baz2a	bromodomain adjacent to zinc finger domain, 2A	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20181227	MGI			
1552099	Baz2a	bromodomain adjacent to zinc finger domain, 2A	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1552099	Baz2a	bromodomain adjacent to zinc finger domain, 2A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20241121	MGI			
1552099	Baz2a	bromodomain adjacent to zinc finger domain, 2A	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20181227	MGI			
1552099	Baz2a	bromodomain adjacent to zinc finger domain, 2A	gene	MP:0004930	small epididymis		IEA		N	RGD:5509061	20181227	MGI			
1552099	Baz2a	bromodomain adjacent to zinc finger domain, 2A	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1552099	Baz2a	bromodomain adjacent to zinc finger domain, 2A	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20181227	MGI			
1552099	Baz2a	bromodomain adjacent to zinc finger domain, 2A	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1552100	Zfp260	zinc finger protein 260	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1552100	Zfp260	zinc finger protein 260	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552100	Zfp260	zinc finger protein 260	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1552100	Zfp260	zinc finger protein 260	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1552100	Zfp260	zinc finger protein 260	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552100	Zfp260	zinc finger protein 260	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1552100	Zfp260	zinc finger protein 260	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201022	MGI			
1552100	Zfp260	zinc finger protein 260	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1552101	Cabp7	calcium binding protein 7	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552101	Cabp7	calcium binding protein 7	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552101	Cabp7	calcium binding protein 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552101	Cabp7	calcium binding protein 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552101	Cabp7	calcium binding protein 7	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552101	Cabp7	calcium binding protein 7	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552101	Cabp7	calcium binding protein 7	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552101	Cabp7	calcium binding protein 7	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552101	Cabp7	calcium binding protein 7	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552101	Cabp7	calcium binding protein 7	gene	MP:0014603	neuromuscular synapse degeneration		IAGP		N	RGD:5509061	20260416	MGI			PMID:38327785
1552102	Tns1	tensin 1	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26301497
1552102	Tns1	tensin 1	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0005526	decreased renal plasma flow rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0009641	kidney degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0010614	abnormal mitral valve cusp morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26301497
1552102	Tns1	tensin 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552102	Tns1	tensin 1	gene	MP:0011534	granular kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:9087448
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20241121	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20241121	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20201022	MGI			PMID:32528174
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201022	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20210520	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20220519	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20220519	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20231207	MGI			
1552103	Ccdc25	coiled-coil domain containing 25	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1552104	Hnrnpll	heterogeneous nuclear ribonucleoprotein L-like	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19100700
1552104	Hnrnpll	heterogeneous nuclear ribonucleoprotein L-like	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19100700
1552104	Hnrnpll	heterogeneous nuclear ribonucleoprotein L-like	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19100700
1552104	Hnrnpll	heterogeneous nuclear ribonucleoprotein L-like	gene	MP:0010833	abnormal memory T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19100700
1552109	Get1	guided entry of tail-anchored proteins factor 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200402	MGI			
1552109	Get1	guided entry of tail-anchored proteins factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552109	Get1	guided entry of tail-anchored proteins factor 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552109	Get1	guided entry of tail-anchored proteins factor 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552114	Wdsub1	WD repeat, SAM and U-box domain containing 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20220811	MGI			
1552114	Wdsub1	WD repeat, SAM and U-box domain containing 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1552114	Wdsub1	WD repeat, SAM and U-box domain containing 1	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20220519	MGI			
1552114	Wdsub1	WD repeat, SAM and U-box domain containing 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1552114	Wdsub1	WD repeat, SAM and U-box domain containing 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1552114	Wdsub1	WD repeat, SAM and U-box domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552114	Wdsub1	WD repeat, SAM and U-box domain containing 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1552115	Smyd1	SET and MYND domain containing 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923873
1552115	Smyd1	SET and MYND domain containing 1	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923873
1552115	Smyd1	SET and MYND domain containing 1	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923873
1552115	Smyd1	SET and MYND domain containing 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923873
1552115	Smyd1	SET and MYND domain containing 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923873
1552115	Smyd1	SET and MYND domain containing 1	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923873
1552115	Smyd1	SET and MYND domain containing 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923873
1552116	Mapre3	microtubule-associated protein, RP/EB family, member 3	gene	MP:0001619	abnormal vascular permeability		IAGP		N	RGD:5509061	20160721	MGI			PMID:26119739
1552116	Mapre3	microtubule-associated protein, RP/EB family, member 3	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20141003	MGI			
1552118	Tspan8	tetraspanin 8	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1552118	Tspan8	tetraspanin 8	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230119	MGI			
1552118	Tspan8	tetraspanin 8	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1552118	Tspan8	tetraspanin 8	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230119	MGI			
1552119	Dhx16	DEAH-box helicase 16	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1552119	Dhx16	DEAH-box helicase 16	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
1552119	Dhx16	DEAH-box helicase 16	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1552119	Dhx16	DEAH-box helicase 16	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552119	Dhx16	DEAH-box helicase 16	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552120	Ghitm	growth hormone inducible transmembrane protein	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:35715207
1552120	Ghitm	growth hormone inducible transmembrane protein	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20230323	MGI			PMID:35715207
1552120	Ghitm	growth hormone inducible transmembrane protein	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20230323	MGI			PMID:35715207
1552120	Ghitm	growth hormone inducible transmembrane protein	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20230323	MGI			PMID:35715207
1552120	Ghitm	growth hormone inducible transmembrane protein	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:35715207
1552123	Srek1	splicing regulatory glutamine/lysine-rich protein 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1552123	Srek1	splicing regulatory glutamine/lysine-rich protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649457
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649457
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649457
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649457
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20220519	MGI			
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15649457
1552126	Adad1	adenosine deaminase domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210128	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20250508	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20250508	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20250508	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210128	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20260402	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1552127	Zfp644	zinc finger protein 644	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1552128	Atg101	autophagy related 101	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1552128	Atg101	autophagy related 101	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1552128	Atg101	autophagy related 101	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1552128	Atg101	autophagy related 101	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1552128	Atg101	autophagy related 101	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1552128	Atg101	autophagy related 101	gene	MP:0010889	small alveolar lamellar bodies		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1552128	Atg101	autophagy related 101	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33296658
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0001726	abnormal allantois morphology		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20201022	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20220519	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20210826	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0009453	enhanced contextual conditioning behavior		IEA		N	RGD:5509061	20260402	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180222	MGI			PMID:16307915
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20241121	MGI			
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0020352	abnormal endoplasmic reticulum physiology		IAGP		N	RGD:5509061	20180222	MGI			PMID:16307915
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0020936	abnormal susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28545059
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0020938	decreased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28545059
1552130	Uggt1	UDP-glucose glycoprotein glucosyltransferase 1	gene	MP:0031039	decreased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:28545059
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0004166	abnormal limbic system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0005267	abnormal olfactory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0006300	abnormal entorhinal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552138	Gm2a	GM2 ganglioside activator protein	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223328
1552139	Vdac2	voltage-dependent anion channel 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20151112	MGI			PMID:19706873
1552139	Vdac2	voltage-dependent anion channel 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20151112	MGI			PMID:19706873
1552139	Vdac2	voltage-dependent anion channel 2	gene	MP:0009258	abnormal thymocyte apoptosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:19706873
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000040	decreased middle ear ossicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000299	failure of atrioventricular cushion closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0003494	parathyroid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0003499	thyroid gland hypoplasia		IAGP		N	RGD:5509061	20150326	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0003798	abnormal Harderian gland pigmentation		IAGP		N	RGD:5509061	20150326	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004159	double aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004318	absent incus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004319	absent malleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004460	alisphenoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004475	palatine bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20170921	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0008023	abnormal styloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0009388	abnormal epidermal melanocyte morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0009525	abnormal submandibular duct morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0009707	absent external auditory canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0009905	absent tongue		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0010191	abnormal choroid melanocyte morphology		IAGP		N	RGD:5509061	20150326	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0010426	abnormal heart and great artery attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0010486	absent right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0010572	persistent right dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0010720	absent sublingual duct		IAGP		N	RGD:5509061	20150326	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0010722	persistent cervical thymus		IAGP		N	RGD:5509061	20150326	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811845
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0012310	persistent ductus caroticus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0013917	persistent right 6th pharyngeal arch artery		IAGP		N	RGD:5509061	20191219	MGI			PMID:9649553
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0030122	temporal bone squamous part hypoplasia		IAGP		N	RGD:5509061	20171005	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0030992	atrioventricular cushion hypoplasia		IAGP		N	RGD:5509061	20191128	MGI			PMID:9449665
1552140	Ece1	endothelin converting enzyme 1	gene	MP:0031550	abnormal atrioventricular valve development		IAGP		N	RGD:5509061	20240104	MGI			PMID:10811845
1552142	Mon1b	MON1 homolog B, secretory traffciking associated	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1552142	Mon1b	MON1 homolog B, secretory traffciking associated	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1552142	Mon1b	MON1 homolog B, secretory traffciking associated	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1552144	Actl6a	actin-like 6A	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20230601	MGI			
1552144	Actl6a	actin-like 6A	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1552144	Actl6a	actin-like 6A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1552144	Actl6a	actin-like 6A	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1552144	Actl6a	actin-like 6A	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1552144	Actl6a	actin-like 6A	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0011903	decreased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23018638
1552144	Actl6a	actin-like 6A	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20250508	MGI			
1552145	Dnajc17	DnaJ heat shock protein family (Hsp40) member C17	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200310	MGI			
1552145	Dnajc17	DnaJ heat shock protein family (Hsp40) member C17	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1552145	Dnajc17	DnaJ heat shock protein family (Hsp40) member C17	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20221215	MGI			
1552145	Dnajc17	DnaJ heat shock protein family (Hsp40) member C17	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20160132
1552145	Dnajc17	DnaJ heat shock protein family (Hsp40) member C17	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0009884	palatal shelf fusion with tongue or mandible		IAGP		N	RGD:5509061	20200310	MGI			PMID:28817352
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28817352
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28817352
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0013530	abnormal periderm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28817352
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0030179	abnormal oral epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28817352
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552150	Arhgap29	Rho GTPase activating protein 29	gene	MP:0031532	abnormal heart ventricle wall morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:40230422
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1606615
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893328
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380515
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893328
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0001690	failure of somite differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893328
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:1606615
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:1606615
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893328
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898232
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702876
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290321
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12702876
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380515
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380515
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940649
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380515
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1606615
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940357
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898232
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12397175
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8608936
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940649
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940649
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0003121	genetic imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679064
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890782
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20230727	MGI			PMID:34516921
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20230727	MGI			PMID:34516921
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:11290321
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:18221528
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679064
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383065
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17893328
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15380515
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898232
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0008011	intestine polyps		IAGP		N	RGD:5509061	20141003	MGI			PMID:11888894
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16940357
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20230727	MGI			PMID:34516921
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20230727	MGI			PMID:34516921
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1606615
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182866
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383065
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898232
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20230727	MGI			PMID:34516921
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898232
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230727	MGI			PMID:34516921
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1606615
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898232
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383065
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890782
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890782
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0012131	small visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:1606615
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0012207	decreased neuronal stem cell self-renewal		IAGP		N	RGD:5509061	20230727	MGI			PMID:34516921
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20230727	MGI			PMID:34516921
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11940649
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:1606615
1552151	Dnmt1	DNA methyltransferase 1	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20230727	MGI			PMID:34516921
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20210401	MGI			PMID:23902639
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20210401	MGI			PMID:23902639
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093357
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20210401	MGI			PMID:23902639
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:23902639
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20240523	MGI			
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0002965	increased circulating serum albumin level		IAGP		N	RGD:5509061	20210401	MGI			PMID:23902639
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20210401	MGI			PMID:23902639
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093357
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20210401	MGI			PMID:23902639
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20210401	MGI			PMID:23902639
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093357
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20210401	MGI			PMID:23902639
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093357
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093357
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0010127	hypervolemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093357
1552153	Agtrap	angiotensin II, type I receptor-associated protein	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20240523	MGI			
1552156	Pon3	paraoxonase 3	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0002830	gallstones		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22441669
1552156	Pon3	paraoxonase 3	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0004773	abnormal bile composition		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0004789	increased bile salt level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21952037
1552156	Pon3	paraoxonase 3	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0009121	increased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21952037
1552156	Pon3	paraoxonase 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21952037
1552156	Pon3	paraoxonase 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21952037
1552156	Pon3	paraoxonase 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21952037
1552156	Pon3	paraoxonase 3	gene	MP:0012338	decreased bile salt level		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0012604	decreased glutathione level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22441669
1552156	Pon3	paraoxonase 3	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20170406	MGI			PMID:25477283
1552156	Pon3	paraoxonase 3	gene	MP:0014910	decreased hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:25477283
1552157	Rnf135	ring finger protein 135	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210826	MGI			
1552157	Rnf135	ring finger protein 135	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20181227	MGI			
1552157	Rnf135	ring finger protein 135	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1552157	Rnf135	ring finger protein 135	gene	MP:0001127	small ovary		IEA		N	RGD:5509061	20210826	MGI			
1552157	Rnf135	ring finger protein 135	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1552157	Rnf135	ring finger protein 135	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1552157	Rnf135	ring finger protein 135	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20210826	MGI			
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19323995
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19109949
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15797020
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647317
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15797020
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19109949
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434421
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:19109949
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19459208
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150430	MGI			PMID:24608965
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19109949
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765429
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632990
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0004165	abnormal lateral geniculate nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19323995
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0004267	abnormal optic tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19323995
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14559155
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141225	MGI			PMID:24736625
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15797020
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006156	abnormal visual pursuit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19323995
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006219	optic nerve degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19109949
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434421
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632990
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006243	impaired pupillary reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765429
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006243	impaired pupillary reflex		IAGP		N	RGD:5509061	20230713	MGI			PMID:19323995
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19323995
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765429
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632990
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19323995
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647317
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18434421
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8637595
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008105	increased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008259	abnormal optic disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15797020
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11807038
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:15797020
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19109949
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632990
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632990
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18321480
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8632990
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0008847	abnormal suprachiasmatic nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765429
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0009639	abnormal olivary pretectal nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21765429
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15797020
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0020468	abnormal circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:21765429
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:19323995
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20171012	MGI			PMID:19323995
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:15647317
1552160	Pou4f2	POU domain, class 4, transcription factor 2	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:18321480
1552161	Muc6	mucin 6, gastric	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20260402	MGI			
1552161	Muc6	mucin 6, gastric	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1552161	Muc6	mucin 6, gastric	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20260402	MGI			
1552161	Muc6	mucin 6, gastric	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20260402	MGI			
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0009827	skin detachment		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552164	Ahdc1	AT hook, DNA binding motif, containing 1	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20240307	MGI			PMID:35585237
1552165	Slc10a6	solute carrier family 10 (sodium/bile acid cotransporter family), member 6	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20210401	MGI			PMID:28743544
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20181122	MGI			PMID:25902485
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978083
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0001830	decreased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351619
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351619
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16688182
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978083
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16688182
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351619
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23034650
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16688182
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16688182
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15657292
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17277169
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978083
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17277169
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978083
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15657292
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978083
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17351619
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978083
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16920909
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20151112	MGI			PMID:22089030
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17277169
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008588	abnormal circulating interleukin level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22089030
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22089030
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15657292
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17277169
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16688182
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20151112	MGI			PMID:22089030
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16920909
1552166	Il23a	interleukin 23, alpha subunit p19	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264109
1552167	Phkb	phosphorylase kinase beta	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201022	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20241121	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20241121	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0002715	decreased glycogen catabolism rate		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0008821	increased blood uric acid level		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552167	Phkb	phosphorylase kinase beta	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552167	Phkb	phosphorylase kinase beta	gene	MP:0030974	enhanced gluconeogenesis		IAGP		N	RGD:5509061	20221124	MGI			PMID:36077341
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20210617	MGI			PMID:30876848
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20210617	MGI			PMID:30876848
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407399
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955448
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:24423059
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28041882
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20210617	MGI			PMID:30876848
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20210617	MGI			PMID:30876848
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0003647	absent oligodendrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0003647	absent oligodendrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407399
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20210617	MGI			PMID:30876848
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0005470	increased thyroxine level		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0005473	decreased triiodothyronine level		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20210617	MGI			PMID:30876848
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20230713	MGI			PMID:26928066
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0009941	abnormal olfactory bulb interneuron morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210617	MGI			PMID:30876848
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151224	MGI			PMID:24507192
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11955447
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407399
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20230713	MGI			PMID:26928066
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20161027	MGI			PMID:27008863
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20180607	MGI			PMID:28041882
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20210617	MGI			PMID:30876848
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20230713	MGI			PMID:26928066
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0014318	abnormal oligodendrocyte differentiation		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1552169	Olig1	oligodendrocyte transcription factor 1	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:11955447
1552170	Incenp	inner centromere protein	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369859
1552170	Incenp	inner centromere protein	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369859
1552170	Incenp	inner centromere protein	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369859
1552170	Incenp	inner centromere protein	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369859
1552170	Incenp	inner centromere protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10369859
1552171	Capsl	calcyphosine-like	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20250605	MGI			PMID:39264149
1552171	Capsl	calcyphosine-like	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20250605	MGI			PMID:39264149
1552171	Capsl	calcyphosine-like	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39264149
1552171	Capsl	calcyphosine-like	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20250605	MGI			PMID:39264149
1552171	Capsl	calcyphosine-like	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39264149
1552171	Capsl	calcyphosine-like	gene	MP:0012201	decreased endothelial cell proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:39264149
1552171	Capsl	calcyphosine-like	gene	MP:0012537	abnormal hyaloid artery morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39264149
1552172	Rlf	rearranged L-myc fusion sequence	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19099580
1552172	Rlf	rearranged L-myc fusion sequence	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:19099580
1552173	Acat2	acetyl-Coenzyme A acetyltransferase 2	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20210128	MGI			
1552173	Acat2	acetyl-Coenzyme A acetyltransferase 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20161201	MGI			
1552173	Acat2	acetyl-Coenzyme A acetyltransferase 2	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1552173	Acat2	acetyl-Coenzyme A acetyltransferase 2	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20161201	MGI			
1552173	Acat2	acetyl-Coenzyme A acetyltransferase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754665
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0000505	decreased digestive secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754665
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0003285	gastric hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084694
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754665
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084694
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754665
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0004151	decreased circulating iron level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0004731	increased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754665
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0008001	hypochlorhydria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754665
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0008003	achlorhydria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754665
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0008003	achlorhydria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084694
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:16754665
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:21084694
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0010092	increased circulating magnesium level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0011891	decreased circulating ferritin level		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0013569	gastric gland hyperplasia		IAGP		N	RGD:5509061	20150312	MGI			PMID:16754665
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0013569	gastric gland hyperplasia		IAGP		N	RGD:5509061	20161027	MGI			PMID:25127743
1552174	Kcne2	potassium voltage-gated channel, Isk-related subfamily, gene 2	gene	MP:0013578	abnormal stomach glandular region morphology		IAGP		N	RGD:5509061	20150312	MGI			PMID:16754665
1552177	Ube2q1	ubiquitin-conjugating enzyme E2Q family member 1	gene	MP:0001377	abnormal mating frequency		IAGP		N	RGD:5509061	20200310	MGI			PMID:23108111
1552177	Ube2q1	ubiquitin-conjugating enzyme E2Q family member 1	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20200310	MGI			PMID:23108111
1552177	Ube2q1	ubiquitin-conjugating enzyme E2Q family member 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23108111
1552177	Ube2q1	ubiquitin-conjugating enzyme E2Q family member 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20200310	MGI			PMID:23108111
1552177	Ube2q1	ubiquitin-conjugating enzyme E2Q family member 1	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23108111
1552177	Ube2q1	ubiquitin-conjugating enzyme E2Q family member 1	gene	MP:0008976	delayed female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:23108111
1552177	Ube2q1	ubiquitin-conjugating enzyme E2Q family member 1	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20200310	MGI			PMID:23108111
1552177	Ube2q1	ubiquitin-conjugating enzyme E2Q family member 1	gene	MP:0011103	embryonic lethality at implantation, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23108111
1552179	Mtr	5-methyltetrahydrofolate-homocysteine methyltransferase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11158293
1552179	Mtr	5-methyltetrahydrofolate-homocysteine methyltransferase	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:11158293
1552179	Mtr	5-methyltetrahydrofolate-homocysteine methyltransferase	gene	MP:0030644	increased circulating methionine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:11158293
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15256493
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15256493
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15256493
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0005149	abnormal gubernaculum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15256493
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15256493
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0009722	abnormal nipple development		IAGP		N	RGD:5509061	20150402	MGI			PMID:15256493
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0011727	ectopic ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:15256493
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0013713	decreased nipple size		IAGP		N	RGD:5509061	20150402	MGI			PMID:14701741
1552181	Rxfp1	relaxin/insulin-like family peptide receptor 1	gene	MP:0013713	decreased nipple size		IAGP		N	RGD:5509061	20150402	MGI			PMID:15256493
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23624557
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:23624557
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23624557
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0005462	abnormal mast cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23624557
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0005535	abnormal body temperature		IAGP		N	RGD:5509061	20200310	MGI			PMID:23624557
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:23624557
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23624557
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0009280	decreased activated sperm motility		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0014467	increased sperm mitochondrial size		IAGP		N	RGD:5509061	20240613	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20240613	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20200310	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0031352	absent sperm axonemal central pair		IAGP		N	RGD:5509061	20220630	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:20424323
1552182	Pla2g3	phospholipase A2, group III	gene	MP:0031410	biflagellated sperm		IAGP		N	RGD:5509061	20220630	MGI			PMID:20424323
1552183	Lemd2	LEM domain containing 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20200310	MGI			
1552183	Lemd2	LEM domain containing 2	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0008932	abnormal embryonic tissue physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0010503	myocardial trabeculae hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1552183	Lemd2	LEM domain containing 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552183	Lemd2	LEM domain containing 2	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20230330	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20250508	MGI			
1552183	Lemd2	LEM domain containing 2	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1552183	Lemd2	LEM domain containing 2	gene	MP:0013906	absent embryonic telencephalon		IAGP		N	RGD:5509061	20200310	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0015067	increased myocardial fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0015069	increased myocardial fiber length		IAGP		N	RGD:5509061	20260813	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0031328	delayed skeletal muscle regeneration		IAGP		N	RGD:5509061	20220106	MGI			PMID:25790465
1552183	Lemd2	LEM domain containing 2	gene	MP:0031756	first degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:36377660
1552183	Lemd2	LEM domain containing 2	gene	MP:0031757	second degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:36377660
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20211209	MGI			PMID:31798959
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211209	MGI			PMID:31798959
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20211209	MGI			PMID:31798959
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20211209	MGI			PMID:31798959
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20211209	MGI			PMID:31798959
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20211209	MGI			PMID:31798959
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20211209	MGI			PMID:31798959
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0020103	decreased hepatic glucose production		IAGP		N	RGD:5509061	20191010	MGI			PMID:31230984
1552184	Or4m1	olfactory receptor family 4 subfamily M member 1	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20211209	MGI			PMID:31798959
1552186	Lyzl6	lysozyme-like 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:27357688
1552188	Galc	galactosylceramidase	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1552188	Galc	galactosylceramidase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20210805	MGI			PMID:34142127
1552188	Galc	galactosylceramidase	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:6319815
1552188	Galc	galactosylceramidase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
1552188	Galc	galactosylceramidase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1552188	Galc	galactosylceramidase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7417782
1552188	Galc	galactosylceramidase	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:7417782
1552188	Galc	galactosylceramidase	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
1552188	Galc	galactosylceramidase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
1552188	Galc	galactosylceramidase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1552188	Galc	galactosylceramidase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10374755
1552188	Galc	galactosylceramidase	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0000958	peripheral nervous system degeneration		IEA		N	RGD:5509061	20111116	MGI			
1552188	Galc	galactosylceramidase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210805	MGI			PMID:34142127
1552188	Galc	galactosylceramidase	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1552188	Galc	galactosylceramidase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1552188	Galc	galactosylceramidase	gene	MP:0001524	impaired limb coordination		IEA		N	RGD:5509061	20111116	MGI			
1552188	Galc	galactosylceramidase	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
1552188	Galc	galactosylceramidase	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:6306338
1552188	Galc	galactosylceramidase	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
1552188	Galc	galactosylceramidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1552188	Galc	galactosylceramidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7417782
1552188	Galc	galactosylceramidase	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6319815
1552188	Galc	galactosylceramidase	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6693925
1552188	Galc	galactosylceramidase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1552188	Galc	galactosylceramidase	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
1552188	Galc	galactosylceramidase	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7417782
1552188	Galc	galactosylceramidase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6306338
1552188	Galc	galactosylceramidase	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7417782
1552188	Galc	galactosylceramidase	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:34142127
1552188	Galc	galactosylceramidase	gene	MP:0004875	increased mean systemic arterial blood pressure		IEA		N	RGD:5509061	20190103	MGI			
1552188	Galc	galactosylceramidase	gene	MP:0004967	abnormal kidney epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6319815
1552188	Galc	galactosylceramidase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7417782
1552188	Galc	galactosylceramidase	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
1552188	Galc	galactosylceramidase	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20190103	MGI			
1552188	Galc	galactosylceramidase	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0005405	axon degeneration		IEA		N	RGD:5509061	20111116	MGI			
1552188	Galc	galactosylceramidase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1552188	Galc	galactosylceramidase	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16624958
1552188	Galc	galactosylceramidase	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11371512
1552188	Galc	galactosylceramidase	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IEA		N	RGD:5509061	20190103	MGI			
1552188	Galc	galactosylceramidase	gene	MP:0008026	abnormal brain white matter morphology		IEA		N	RGD:5509061	20111116	MGI			
1552188	Galc	galactosylceramidase	gene	MP:0008027	abnormal spinal cord white matter morphology		IEA		N	RGD:5509061	20111116	MGI			
1552188	Galc	galactosylceramidase	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6693925
1552188	Galc	galactosylceramidase	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23620143
1552188	Galc	galactosylceramidase	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
1552188	Galc	galactosylceramidase	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0008917	abnormal oligodendrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0009046	muscle twitch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861297
1552188	Galc	galactosylceramidase	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10374755
1552188	Galc	galactosylceramidase	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0009978	abnormal cerebellum white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10415153
1552188	Galc	galactosylceramidase	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20141003	MGI			PMID:12270695
1552188	Galc	galactosylceramidase	gene	MP:0010170	abnormal glial cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10374755
1552188	Galc	galactosylceramidase	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0010892	increased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21389217
1552188	Galc	galactosylceramidase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1552188	Galc	galactosylceramidase	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0014966	decreased heart enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0014972	decreased spleen enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0014975	decreased kidney enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:11461188
1552188	Galc	galactosylceramidase	gene	MP:0030825	decreased femur size		IAGP		N	RGD:5509061	20181018	MGI			PMID:20441793
1552188	Galc	galactosylceramidase	gene	MP:0030826	decreased femur weight		IAGP		N	RGD:5509061	20181018	MGI			PMID:20441793
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000100	abnormal ethmoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467597
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002068	abnormal parental behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467597
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002244	abnormal turbinate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002244	abnormal turbinate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002729	abnormal inner ear canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002894	abnormal otolith morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003069	abnormal superior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003143	enlarged otoliths		IAGP		N	RGD:5509061	20151001	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003144	decreased otolith number		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003164	decreased posterior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003169	abnormal scala media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004105	cornea abrasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18436818
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18436818
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004409	abnormal crista ampullaris neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004477	turbinate hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004681	intervertebral disk hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16824956
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18436818
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18436818
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:18467597
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16824956
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008052	abnormal serous gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008170	decreased B-1b cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008194	abnormal memory B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009727	abnormal navicular morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009892	palate bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126927
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18436818
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18436818
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16598713
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20230810	MGI			PMID:18436818
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20240627	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0013945	abnormal elbow joint morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0014012	abnormal cranial blood vasculature morphology		IAGP		N	RGD:5509061	20170713	MGI			PMID:28176446
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0014806	humeroradial synostosis		IAGP		N	RGD:5509061	20251120	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20150702	MGI			
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0020858	cornea epithelium hypoplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:18436818
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0021208	median cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0021211	unilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0030259	mandibular condyloid process hypoplasia		IAGP		N	RGD:5509061	20171207	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0030285	mandibular coronoid process hypoplasia		IAGP		N	RGD:5509061	20171207	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0030304	abnormal cribriform plate morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0030373	Meckel's cartilage hyperplasia		IAGP		N	RGD:5509061	20171207	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0030829	abnormal hip joint morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0030860	patellar dislocation		IAGP		N	RGD:5509061	20181025	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0030897	abnormal humeroulnar joint morphology		IAGP		N	RGD:5509061	20251120	MGI			PMID:9389660
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:21980308
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0031447	unilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0031447	unilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:11776395
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0031447	unilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:13539273
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:10669096
1552190	Zeb1	zinc finger E-box binding homeobox 1	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:10669096
1552191	Wif1	Wnt inhibitory factor 1	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19307728
1552191	Wif1	Wnt inhibitory factor 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19307728
1552191	Wif1	Wnt inhibitory factor 1	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19307728
1552191	Wif1	Wnt inhibitory factor 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19307728
1552198	Ms4a2	membrane-spanning 4-domains, subfamily A, member 2	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069418
1552198	Ms4a2	membrane-spanning 4-domains, subfamily A, member 2	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9586641
1552198	Ms4a2	membrane-spanning 4-domains, subfamily A, member 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9586641
1552198	Ms4a2	membrane-spanning 4-domains, subfamily A, member 2	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10069418
1552198	Ms4a2	membrane-spanning 4-domains, subfamily A, member 2	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:9586641
1552198	Ms4a2	membrane-spanning 4-domains, subfamily A, member 2	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20260402	MGI			
1552199	Entpd6	ectonucleoside triphosphate diphosphohydrolase 6	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20201022	MGI			
1552199	Entpd6	ectonucleoside triphosphate diphosphohydrolase 6	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1552199	Entpd6	ectonucleoside triphosphate diphosphohydrolase 6	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20150430	MGI			
1552199	Entpd6	ectonucleoside triphosphate diphosphohydrolase 6	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1552199	Entpd6	ectonucleoside triphosphate diphosphohydrolase 6	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093629
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093629
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093629
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20190228	MGI			PMID:29306897
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20190228	MGI			PMID:29306897
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093629
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20190228	MGI			PMID:29306897
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0004011	decreased diastolic filling velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0004117	abnormal atrioventricular bundle morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:29306897
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0004124	abnormal Purkinje fiber morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:29306897
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093629
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0004565	decreased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20190228	MGI			PMID:29306897
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0010640	ventricular myocardium compact layer hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360251
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0012624	decreased acetylcholinesterase activity		IAGP		N	RGD:5509061	20190228	MGI			PMID:29306897
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0020345	abnormal myocardial fiber currents		IAGP		N	RGD:5509061	20190228	MGI			PMID:29306897
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0031717	prolonged corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:29306897
1552200	Xirp2	xin actin-binding repeat containing 2	gene	MP:0031762	third degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:29306897
1552201	Neurog3	neurogenin 3	gene	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19487660
1552201	Neurog3	neurogenin 3	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19487660
1552201	Neurog3	neurogenin 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297605
1552201	Neurog3	neurogenin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0002691	small stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:12080087
1552201	Neurog3	neurogenin 3	gene	MP:0002791	steatorrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0003016	increased circulating bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19487660
1552201	Neurog3	neurogenin 3	gene	MP:0003867	increased defecation amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0005210	disorganized stomach mucosa		IAGP		N	RGD:5509061	20141003	MGI			PMID:12080087
1552201	Neurog3	neurogenin 3	gene	MP:0005211	increased stomach mucosa thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12080087
1552201	Neurog3	neurogenin 3	gene	MP:0005214	regional gastric metaplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12080087
1552201	Neurog3	neurogenin 3	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394599
1552201	Neurog3	neurogenin 3	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12080087
1552201	Neurog3	neurogenin 3	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12080087
1552201	Neurog3	neurogenin 3	gene	MP:0005218	abnormal pancreatic delta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12080087
1552201	Neurog3	neurogenin 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19487660
1552201	Neurog3	neurogenin 3	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19487660
1552201	Neurog3	neurogenin 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0006001	abnormal intestinal transit time		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0008109	abnormal small intestinal microvillus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0008141	decreased small intestinal microvillus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0009161	pancreatic acinar cell zymogen granule accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0009165	abnormal endocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223466
1552201	Neurog3	neurogenin 3	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0009173	absent pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0009174	absent pancreatic beta cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0009178	absent pancreatic alpha cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0010158	abnormal intestine development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0010802	abnormal intestinal enteroendocrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10677506
1552201	Neurog3	neurogenin 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20364088
1552201	Neurog3	neurogenin 3	gene	MP:0011984	decreased enteroendocrine cell number		IAGP		N	RGD:5509061	20210603	MGI			PMID:31663849
1552204	Sstr2	somatostatin receptor 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20210520	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029646
1552204	Sstr2	somatostatin receptor 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029646
1552204	Sstr2	somatostatin receptor 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752788
1552204	Sstr2	somatostatin receptor 2	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029646
1552204	Sstr2	somatostatin receptor 2	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029646
1552204	Sstr2	somatostatin receptor 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20201022	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11029646
1552204	Sstr2	somatostatin receptor 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20241121	MGI			
1552204	Sstr2	somatostatin receptor 2	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601946
1552204	Sstr2	somatostatin receptor 2	gene	MP:0004494	abnormal synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752788
1552204	Sstr2	somatostatin receptor 2	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752788
1552204	Sstr2	somatostatin receptor 2	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15548214
1552204	Sstr2	somatostatin receptor 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12752788
1552204	Sstr2	somatostatin receptor 2	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14750962
1552204	Sstr2	somatostatin receptor 2	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17425570
1552205	Tmem62	transmembrane protein 62	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1552205	Tmem62	transmembrane protein 62	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1552206	Tm2d1	TM2 domain containing 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200310	MGI			
1552206	Tm2d1	TM2 domain containing 1	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1552206	Tm2d1	TM2 domain containing 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20201022	MGI			
1552206	Tm2d1	TM2 domain containing 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1552206	Tm2d1	TM2 domain containing 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20200402	MGI			
1552206	Tm2d1	TM2 domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781238
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781238
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781238
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781238
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781238
1552207	Pla2g15	phospholipase A2, group XV	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16880524
1552209	Has1	hyaluronan synthase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20823158
1552209	Has1	hyaluronan synthase 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552209	Has1	hyaluronan synthase 1	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1552210	Osmr	oncostatin M receptor	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855584
1552210	Osmr	oncostatin M receptor	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855584
1552210	Osmr	oncostatin M receptor	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855584
1552210	Osmr	oncostatin M receptor	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855584
1552210	Osmr	oncostatin M receptor	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855584
1552210	Osmr	oncostatin M receptor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855584
1552210	Osmr	oncostatin M receptor	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855584
1552210	Osmr	oncostatin M receptor	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855584
1552210	Osmr	oncostatin M receptor	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855584
1552210	Osmr	oncostatin M receptor	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141106	MGI			PMID:24695736
1552210	Osmr	oncostatin M receptor	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240321	MGI			PMID:24695736
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778975
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778975
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778975
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0002163	abnormal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778975
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15778975
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0004757	abnormal distal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0005310	abnormal salivary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0011754	abnormal kidney collecting duct intercalated cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17079272
1552211	Tfcp2l1	transcription factor CP2-like 1	gene	MP:0013580	abnormal nasal gland morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:17079272
1552216	Ppm1k	protein phosphatase 1K (PP2C domain containing)	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:19411760
1552216	Ppm1k	protein phosphatase 1K (PP2C domain containing)	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19411760
1552216	Ppm1k	protein phosphatase 1K (PP2C domain containing)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19411760
1552220	Gtf2h3	general transcription factor IIH, polypeptide 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210826	MGI			
1552220	Gtf2h3	general transcription factor IIH, polypeptide 3	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20250508	MGI			
1552220	Gtf2h3	general transcription factor IIH, polypeptide 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1552220	Gtf2h3	general transcription factor IIH, polypeptide 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220811	MGI			
1552223	Lmo7	LIM domain only 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761045
1552223	Lmo7	LIM domain only 7	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19215226
1552223	Lmo7	LIM domain only 7	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761045
1552223	Lmo7	LIM domain only 7	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761045
1552223	Lmo7	LIM domain only 7	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761045
1552223	Lmo7	LIM domain only 7	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761045
1552223	Lmo7	LIM domain only 7	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761045
1552223	Lmo7	LIM domain only 7	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761045
1552223	Lmo7	LIM domain only 7	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761045
1552223	Lmo7	LIM domain only 7	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19215226
1552223	Lmo7	LIM domain only 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12761045
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221020	MGI			PMID:33772547
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20141003	MGI			
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17150957
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0005222	abnormal somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221020	MGI			PMID:33772547
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0010487	abnormal right subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0010488	abnormal left subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:33772547
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645126
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451234
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20221020	MGI			PMID:33772547
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0021208	median cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:33772547
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:33772547
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0030191	narrow snout		IEA		N	RGD:5509061	20171019	MGI			
1552225	Rere	arginine glutamic acid dipeptide (RE) repeats	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:33772547
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000650	mesocardia		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160421	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20160421	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003130	anal atresia		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20160811	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20160811	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20160811	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260402	MGI			PMID:39201474
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004159	double aortic arch		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004651	increased thoracic vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004653	absent caudal vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004656	absent sacral vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004694	absent patella		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0005155	herniated intestine		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20160811	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0008999	absent anus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0010413	complete atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0010466	vascular ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011055	abnormal respiratory motile cilium physiology		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18378898
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354705
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011649	immotile respiratory cilia		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011665	d-loop transposition of the great arteries		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0011872	absent xiphoid process		IAGP		N	RGD:5509061	20231130	MGI			PMID:18519639
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1552230	Pcsk5	proprotein convertase subtilisin/kexin type 5	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:18519639
1552231	Stac2	SH3 and cysteine rich domain 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0008891	decreased hepatocyte apoptosis		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0014903	decreased circulating CCL2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:38478630
1552232	Ms4a7	membrane-spanning 4-domains, subfamily A, member 7	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20240530	MGI			PMID:38478630
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0002999	abnormal bone healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0013624	decreased femur compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0013633	decreased femur maximal load		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0013646	decreased energy dissipated prior to femur fracture		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552233	Clec11a	C-type lectin domain family 11, member a	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:27976999
1552235	Panx1	pannexin 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606493
1552235	Panx1	pannexin 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21508259
1552235	Panx1	pannexin 1	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949881
1552235	Panx1	pannexin 1	gene	MP:0002983	increased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384122
1552235	Panx1	pannexin 1	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384122
1552235	Panx1	pannexin 1	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22147915
1552235	Panx1	pannexin 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949881
1552235	Panx1	pannexin 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20220811	MGI			
1552235	Panx1	pannexin 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384122
1552235	Panx1	pannexin 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210520	MGI			
1552235	Panx1	pannexin 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1552235	Panx1	pannexin 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606493
1552235	Panx1	pannexin 1	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22147915
1552235	Panx1	pannexin 1	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22147915
1552235	Panx1	pannexin 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1552236	Or5ar1	olfactory receptor family 5 subfamily AR member 1	gene	MP:0020421	increased freezing behavior		IAGP		N	RGD:5509061	20210401	MGI			PMID:28685774
1552236	Or5ar1	olfactory receptor family 5 subfamily AR member 1	gene	MP:0020422	decreased freezing behavior		IAGP		N	RGD:5509061	20210401	MGI			PMID:28685774
1552237	Ihh	Indian hedgehog	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252479
1552237	Ihh	Indian hedgehog	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
1552237	Ihh	Indian hedgehog	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155527
1552237	Ihh	Indian hedgehog	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881493
1552237	Ihh	Indian hedgehog	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881493
1552237	Ihh	Indian hedgehog	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:15075292
1552237	Ihh	Indian hedgehog	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252479
1552237	Ihh	Indian hedgehog	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15075292
1552237	Ihh	Indian hedgehog	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155527
1552237	Ihh	Indian hedgehog	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20171221	MGI			PMID:28696225
1552237	Ihh	Indian hedgehog	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881493
1552237	Ihh	Indian hedgehog	gene	MP:0003271	abnormal duodenum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0003283	abnormal digestive organ placement		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252479
1552237	Ihh	Indian hedgehog	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155527
1552237	Ihh	Indian hedgehog	gene	MP:0004053	abnormal synchondrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17881493
1552237	Ihh	Indian hedgehog	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20230223	MGI			PMID:21364421
1552237	Ihh	Indian hedgehog	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252479
1552237	Ihh	Indian hedgehog	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0006261	annular pancreas		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821773
1552237	Ihh	Indian hedgehog	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252479
1552237	Ihh	Indian hedgehog	gene	MP:0006322	abnormal perichondrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
1552237	Ihh	Indian hedgehog	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951842
1552237	Ihh	Indian hedgehog	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155527
1552237	Ihh	Indian hedgehog	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22155527
1552237	Ihh	Indian hedgehog	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19252479
1552237	Ihh	Indian hedgehog	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20171221	MGI			PMID:28696225
1552237	Ihh	Indian hedgehog	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0010969	absent compact bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16278811
1552237	Ihh	Indian hedgehog	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906844
1552237	Ihh	Indian hedgehog	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0011585	decreased alkaline phosphatase activity		IAGP		N	RGD:5509061	20230223	MGI			PMID:21364421
1552237	Ihh	Indian hedgehog	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:11748145
1552237	Ihh	Indian hedgehog	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:15951842
1552237	Ihh	Indian hedgehog	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:10465785
1552237	Ihh	Indian hedgehog	gene	MP:0020516	abnormal visceral yolk sac mesenchyme morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:17881493
1552237	Ihh	Indian hedgehog	gene	MP:0021208	median cleft palate		IAGP		N	RGD:5509061	20230223	MGI			PMID:21364421
1552237	Ihh	Indian hedgehog	gene	MP:0021217	abnormal palatal shelf bone ossification		IAGP		N	RGD:5509061	20230223	MGI			PMID:21364421
1552239	H2-Q10	histocompatibility 2, Q region locus 10	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20231207	MGI			
1552239	H2-Q10	histocompatibility 2, Q region locus 10	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:30537346
1552239	H2-Q10	histocompatibility 2, Q region locus 10	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:30537346
1552239	H2-Q10	histocompatibility 2, Q region locus 10	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:30537346
1552239	H2-Q10	histocompatibility 2, Q region locus 10	gene	MP:0011625	cystolithiasis		IEA		N	RGD:5509061	20231207	MGI			
1552239	H2-Q10	histocompatibility 2, Q region locus 10	gene	MP:0013666	decreased immature NK cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:30537346
1552239	H2-Q10	histocompatibility 2, Q region locus 10	gene	MP:0013672	decreased mature NK cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:30537346
1552240	Gykl1	glycerol kinase-like 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:28852571
1552240	Gykl1	glycerol kinase-like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:28852571
1552240	Gykl1	glycerol kinase-like 1	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20200310	MGI			PMID:28852571
1552240	Gykl1	glycerol kinase-like 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:28852571
1552240	Gykl1	glycerol kinase-like 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28852571
1552240	Gykl1	glycerol kinase-like 1	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:28852571
1552240	Gykl1	glycerol kinase-like 1	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28852571
1552240	Gykl1	glycerol kinase-like 1	gene	MP:0014464	decreased sperm mitochondrial sheath size		IAGP		N	RGD:5509061	20240613	MGI			PMID:28852571
1552242	Eif2b3	eukaryotic translation initiation factor 2B, subunit 3	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1552242	Eif2b3	eukaryotic translation initiation factor 2B, subunit 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1552242	Eif2b3	eukaryotic translation initiation factor 2B, subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552242	Eif2b3	eukaryotic translation initiation factor 2B, subunit 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552242	Eif2b3	eukaryotic translation initiation factor 2B, subunit 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539485
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15563592
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539485
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539485
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275784
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539485
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15563592
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590036
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20240523	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539485
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590036
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20260402	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20231207	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590036
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0002999	abnormal bone healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275784
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15563592
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20240523	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539485
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20240523	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17275784
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590036
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20241121	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19590036
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15563592
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0006399	abnormal long bone epiphyseal ossification zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539485
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20240523	MGI			
1552243	Mmp13	matrix metallopeptidase 13	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15563592
1552244	Etfbkmt	electron transfer flavoprotein beta subunit lysine methyltransferase	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20190307	MGI			PMID:29352221
1552244	Etfbkmt	electron transfer flavoprotein beta subunit lysine methyltransferase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20190307	MGI			PMID:29352221
1552244	Etfbkmt	electron transfer flavoprotein beta subunit lysine methyltransferase	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20190307	MGI			PMID:29352221
1552244	Etfbkmt	electron transfer flavoprotein beta subunit lysine methyltransferase	gene	MP:0014173	increased fatty acid beta-oxidation		IAGP		N	RGD:5509061	20190307	MGI			PMID:29352221
1552244	Etfbkmt	electron transfer flavoprotein beta subunit lysine methyltransferase	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20190307	MGI			PMID:29352221
1552246	Rcor2	REST corepressor 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1552246	Rcor2	REST corepressor 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1552246	Rcor2	REST corepressor 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1552246	Rcor2	REST corepressor 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1552246	Rcor2	REST corepressor 2	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1552246	Rcor2	REST corepressor 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1552246	Rcor2	REST corepressor 2	gene	MP:0009974	decreased cerebral cortex pyramidal cell number		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1552246	Rcor2	REST corepressor 2	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1552250	Axin1	axin 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0000151	absent ribs		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:13340237
1552250	Axin1	axin 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:13340237
1552250	Axin1	axin 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0000585	kinked tail		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20200310	MGI			PMID:21003499
1552250	Axin1	axin 1	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0001675	abnormal ectoderm development		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0001684	abnormal axial mesoderm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9230313
1552250	Axin1	axin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21344612
1552250	Axin1	axin 1	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18113441
1552250	Axin1	axin 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:21003499
1552250	Axin1	axin 1	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0002084	abnormal developmental patterning		IEA		N	RGD:5509061	20200310	MGI			
1552250	Axin1	axin 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18113441
1552250	Axin1	axin 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21344612
1552250	Axin1	axin 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18113441
1552250	Axin1	axin 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11170344
1552250	Axin1	axin 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:13340237
1552250	Axin1	axin 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21003499
1552250	Axin1	axin 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15899843
1552250	Axin1	axin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:21344612
1552250	Axin1	axin 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0003050	abnormal sacral vertebrae morphology		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0003121	genetic imprinting		IAGP		N	RGD:5509061	20200310	MGI			PMID:12601169
1552250	Axin1	axin 1	gene	MP:0003121	genetic imprinting		IAGP		N	RGD:5509061	20200310	MGI			PMID:7276510
1552250	Axin1	axin 1	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20200310	MGI			PMID:12601169
1552250	Axin1	axin 1	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20200310	MGI			PMID:12601169
1552250	Axin1	axin 1	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20200310	MGI			PMID:7276510
1552250	Axin1	axin 1	gene	MP:0003123	paternal imprinting		IAGP		N	RGD:5509061	20230601	MGI			PMID:24265074
1552250	Axin1	axin 1	gene	MP:0003176	reversion by viral sequence excision		IAGP		N	RGD:5509061	20200310	MGI			PMID:11132407
1552250	Axin1	axin 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0003591	urethra atresia		IAGP		N	RGD:5509061	20200310	MGI			PMID:13340237
1552250	Axin1	axin 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18113441
1552250	Axin1	axin 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20200310	MGI			PMID:18113441
1552250	Axin1	axin 1	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0004619	caudal vertebral fusion		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0004621	lumbar vertebral fusion		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0004622	sacral vertebral fusion		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0004623	thoracic vertebral fusion		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0004713	split notochord		IAGP		N	RGD:5509061	20200310	MGI			PMID:18113441
1552250	Axin1	axin 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:21344612
1552250	Axin1	axin 1	gene	MP:0009352	impaired spacing of implantation sites		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0009353	twin decidual capsule		IEA		N	RGD:5509061	20111116	MGI			
1552250	Axin1	axin 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18113441
1552250	Axin1	axin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19204372
1552250	Axin1	axin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0011775	rectal atresia		IAGP		N	RGD:5509061	20200310	MGI			PMID:13340237
1552250	Axin1	axin 1	gene	MP:0011999	abnormal tail length		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552250	Axin1	axin 1	gene	MP:0012062	small tail bud		IAGP		N	RGD:5509061	20200310	MGI			PMID:18113441
1552250	Axin1	axin 1	gene	MP:0012104	small amniotic cavity		IEA		N	RGD:5509061	20200310	MGI			
1552250	Axin1	axin 1	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0012156	rostral-caudal axis duplication		IAGP		N	RGD:5509061	20200310	MGI			PMID:18113441
1552250	Axin1	axin 1	gene	MP:0012156	rostral-caudal axis duplication		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0012174	flat head		IAGP		N	RGD:5509061	20200310	MGI			PMID:8536979
1552250	Axin1	axin 1	gene	MP:0013175	bifurcated tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:17246824
1552252	Septin7	septin 7	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20150910	MGI			PMID:25122120
1552252	Septin7	septin 7	gene	MP:0003707	increased cell nucleus count		IAGP		N	RGD:5509061	20150910	MGI			PMID:25122120
1552252	Septin7	septin 7	gene	MP:0003903	increased cell mass		IAGP		N	RGD:5509061	20150910	MGI			PMID:25122120
1552252	Septin7	septin 7	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113571
1552252	Septin7	septin 7	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24113571
1552252	Septin7	septin 7	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:25122120
1552252	Septin7	septin 7	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20150910	MGI			PMID:25122120
1552252	Septin7	septin 7	gene	MP:0013289	abnormal mitotic cytokinesis		IAGP		N	RGD:5509061	20150910	MGI			PMID:25122120
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15100286
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20161216	MGI			PMID:27708076
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20161216	MGI			PMID:27708076
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20161216	MGI			PMID:27708076
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15100286
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20161216	MGI			PMID:27708076
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20190221	MGI			PMID:30580966
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20180726	MGI			PMID:28783703
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20180726	MGI			PMID:28783703
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671660
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671660
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15100286
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15100286
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15100286
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0008493	alpha-synuclein inclusion body		IAGP		N	RGD:5509061	20161216	MGI			PMID:27708076
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20180726	MGI			PMID:28783703
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20180726	MGI			PMID:28783703
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8602528
1552253	Lag3	lymphocyte-activation gene 3	gene	MP:0013762	abnormal effector T cell number		IAGP		N	RGD:5509061	20180726	MGI			PMID:28783703
1552255	Zfp410	zinc finger protein 410	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240516	MGI			PMID:33859416
1552257	Ctnnd1	catenin delta 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221027	MGI			PMID:29805042
1552257	Ctnnd1	catenin delta 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18809907
1552257	Ctnnd1	catenin delta 1	gene	MP:0000424	retarded hair growth		IAGP		N	RGD:5509061	20200310	MGI			PMID:18809907
1552257	Ctnnd1	catenin delta 1	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18809907
1552257	Ctnnd1	catenin delta 1	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16399075
1552257	Ctnnd1	catenin delta 1	gene	MP:0002235	abnormal external nares morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:29805042
1552257	Ctnnd1	catenin delta 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0003708	binucleate		IAGP		N	RGD:5509061	20200310	MGI			PMID:18809907
1552257	Ctnnd1	catenin delta 1	gene	MP:0003792	abnormal major salivary gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16399075
1552257	Ctnnd1	catenin delta 1	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16399075
1552257	Ctnnd1	catenin delta 1	gene	MP:0004035	abnormal sublingual gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16399075
1552257	Ctnnd1	catenin delta 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18809907
1552257	Ctnnd1	catenin delta 1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20221027	MGI			PMID:29805042
1552257	Ctnnd1	catenin delta 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16815331
1552257	Ctnnd1	catenin delta 1	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0009051	dilated distal convoluted tubule		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18809907
1552257	Ctnnd1	catenin delta 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221027	MGI			PMID:29805042
1552257	Ctnnd1	catenin delta 1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16815331
1552257	Ctnnd1	catenin delta 1	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18809907
1552257	Ctnnd1	catenin delta 1	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:29805042
1552257	Ctnnd1	catenin delta 1	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16399075
1552257	Ctnnd1	catenin delta 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0013300	abnormal submandibular gland physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16399075
1552257	Ctnnd1	catenin delta 1	gene	MP:0013540	increased submandibular gland apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16399075
1552257	Ctnnd1	catenin delta 1	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:21521738
1552257	Ctnnd1	catenin delta 1	gene	MP:0021164	oral cleft		IAGP		N	RGD:5509061	20221027	MGI			PMID:29805042
1552257	Ctnnd1	catenin delta 1	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:29805042
1552257	Ctnnd1	catenin delta 1	gene	MP:0021211	unilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:29805042
1552257	Ctnnd1	catenin delta 1	gene	MP:0030099	facial asymmetry		IAGP		N	RGD:5509061	20221027	MGI			PMID:29805042
1552257	Ctnnd1	catenin delta 1	gene	MP:0030115	abnormal nasal tip morphology		IAGP		N	RGD:5509061	20221027	MGI			PMID:29805042
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19829704
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19829704
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20530548
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20530548
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0004063	dilated heart left atrium		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0005406	abnormal heart size		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:19829704
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20200310	MGI			PMID:19829704
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:19829704
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19829704
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010224	abnormal heart ventricle outflow tract morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20530548
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010591	enlarged aortic valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010600	enlarged pulmonary valve		IAGP		N	RGD:5509061	20200310	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010600	enlarged pulmonary valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010618	enlarged mitral valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010620	thick mitral valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010627	enlarged tricuspid valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0010629	thick tricuspid valve		IAGP		N	RGD:5509061	20231221	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:19829704
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031550	abnormal atrioventricular valve development		IAGP		N	RGD:5509061	20240104	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031555	abnormal pulmonary valve development		IAGP		N	RGD:5509061	20240104	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031570	enlarged atrioventricular valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031570	enlarged atrioventricular valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031570	enlarged atrioventricular valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031575	atrioventricular valve stenosis		IAGP		N	RGD:5509061	20240125	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031580	enlarged semilunar valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:12621152
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031580	enlarged semilunar valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031580	enlarged semilunar valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:14597776
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031585	semilunar valve stenosis		IAGP		N	RGD:5509061	20240125	MGI			PMID:12773386
1552258	Hbegf	heparin-binding EGF-like growth factor	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:14597776
1552259	Gas7	growth arrest specific 7	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1552259	Gas7	growth arrest specific 7	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20160225	MGI			PMID:22662195
1552259	Gas7	growth arrest specific 7	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20160225	MGI			PMID:22662195
1552259	Gas7	growth arrest specific 7	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:22662195
1552259	Gas7	growth arrest specific 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160225	MGI			PMID:22662195
1552259	Gas7	growth arrest specific 7	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1552259	Gas7	growth arrest specific 7	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:22662195
1552259	Gas7	growth arrest specific 7	gene	MP:0004243	abnormal motor nerve collateral sprouting		IAGP		N	RGD:5509061	20160225	MGI			PMID:22662195
1552259	Gas7	growth arrest specific 7	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1552259	Gas7	growth arrest specific 7	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20160225	MGI			PMID:22662195
1552259	Gas7	growth arrest specific 7	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20160225	MGI			PMID:22662195
1552259	Gas7	growth arrest specific 7	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1552259	Gas7	growth arrest specific 7	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160225	MGI			PMID:22662195
1552259	Gas7	growth arrest specific 7	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1552260	Rpl22l1	ribosomal protein L22 like 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:28076796
1552260	Rpl22l1	ribosomal protein L22 like 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28076796
1552261	Slc45a3	solute carrier family 45, member 3	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230720	MGI			
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16730350
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16730350
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16730350
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16730350
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:16730350
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20200310	MGI			PMID:16730350
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0008365	adenohypophysis hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16730350
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0011184	absent embryonic epiblast		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552262	Lin9	lin-9 DREAM MuvB core complex component	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20404087
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0003271	abnormal duodenum morphology		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0003402	decreased liver weight		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230119	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463252
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20240523	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:23452856
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020468	abnormal circadian behavior period		IAGP		N	RGD:5509061	20200310	MGI			PMID:23471982
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20200310	MGI			PMID:15248865
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20200310	MGI			PMID:17462724
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463252
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20200310	MGI			PMID:23452855
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20200310	MGI			PMID:23452856
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20200310	MGI			PMID:23471982
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020475	delayed circadian behavior phase		IEA		N	RGD:5509061	20200310	MGI			
1552263	Fbxl3	F-box and leucine-rich repeat protein 3	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20200310	MGI			PMID:23452856
1552264	Qrsl1	glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1552264	Qrsl1	glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1552264	Qrsl1	glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15741318
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15741318
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15741318
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15741318
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15741318
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15741318
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0008389	hypochromic macrocytic anemia		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15741318
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0011285	increased circulating erythropoietin level		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260611	MGI			PMID:27622333
1552266	Sf3b1	splicing factor 3b, subunit 1	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20220602	MGI			PMID:25481243
1552268	Allc	allantoicase	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20201022	MGI			PMID:32588039
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000540	abnormal urinary bladder urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0000767	abnormal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22781001
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22781001
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22781001
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002534	abnormal type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210520	MGI			
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22781001
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0003630	abnormal urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210520	MGI			
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0004972	abnormal regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22781001
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20190801	MGI			PMID:28165339
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0006418	abnormal testis cord formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20190801	MGI			PMID:28165339
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20190801	MGI			PMID:28165339
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23544080
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0009370	decreased theca cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0011385	abnormal testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0013591	thymus medulla hyperplasia		IAGP		N	RGD:5509061	20150326	MGI			PMID:19119317
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:19056881
1552269	Sgpl1	sphingosine phosphate lyase 1	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:17143286
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20181227	MGI			
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210520	MGI			
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20884616
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20884616
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20884616
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20884616
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20884616
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20884616
1552274	Nme2	NME/NM23 nucleoside diphosphate kinase 2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20884616
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7683855
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7683855
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10191135
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201022	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210520	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:7683855
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10191135
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:1639406
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20221215	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1639406
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7683855
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7683855
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8282051
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3783318
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8282051
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9600738
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0008455	abnormal retina rod cell inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8282051
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8282051
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8282051
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:8282051
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:8282051
1552276	Cln8	CLN8 transmembrane ER and ERGIC protein	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:8282051
1552279	Adam1a	a disintegrin and metallopeptidase domain 1a	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15194697
1552279	Adam1a	a disintegrin and metallopeptidase domain 1a	gene	MP:0005410	abnormal fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15194697
1552279	Adam1a	a disintegrin and metallopeptidase domain 1a	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:15194697
1552279	Adam1a	a disintegrin and metallopeptidase domain 1a	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20200227	MGI			PMID:15194697
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0000958	peripheral nervous system degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689132
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19116659
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10461886
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9398473
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689132
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0008503	abnormal spinal cord grey matter morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552280	Nefl	neurofilament, light polypeptide	gene	MP:0014062	nervous system inclusion bodies		IAGP		N	RGD:5509061	20160324	MGI			PMID:25552649
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:16502419
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17227850
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17717145
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17227850
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17227850
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20200310	MGI			PMID:17717145
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17227850
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17622570
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17227850
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17717145
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0010537	tumor regression		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17227850
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:19956687
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011140	decreased lung endothelial cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17717145
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011141	increased lung endothelial cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17717145
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20240405	MGI			PMID:34434211
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0020321	increased vascular endothelial cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17717145
1552283	Id1	inhibitor of DNA binding 1, HLH protein	gene	MP:0030410	middle ear effusion		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10440905
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855597
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10440905
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10527801
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10527801
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201210	MGI			PMID:32601357
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326100
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855597
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20201210	MGI			PMID:32601357
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219947
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855597
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219947
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219947
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10527801
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855597
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10440905
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32601357
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20160825	MGI			PMID:27101989
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20160825	MGI			PMID:27101989
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855597
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219947
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855597
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:32601357
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326100
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10440905
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10527801
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17855597
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32601357
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326100
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10527801
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219947
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219947
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10527801
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0008195	abnormal professional antigen presenting cell morphology		IAGP		N	RGD:5509061	20160825	MGI			PMID:27101989
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20219947
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12374761
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20160825	MGI			PMID:27101989
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0014695	increased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:27101989
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0014961	increased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:32601357
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:32601357
1552285	Cln3	CLN3 lysosomal/endosomal transmembrane protein, battenin	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20201210	MGI			PMID:32601357
1552286	Nudt21	nudix hydrolase 21	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:30830875
1552286	Nudt21	nudix hydrolase 21	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:30830875
1552286	Nudt21	nudix hydrolase 21	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:30830875
1552286	Nudt21	nudix hydrolase 21	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552286	Nudt21	nudix hydrolase 21	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552286	Nudt21	nudix hydrolase 21	gene	MP:0020253	increased collagen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30830875
1552290	Flywch1	FLYWCH-type zinc finger 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200310	MGI			
1552290	Flywch1	FLYWCH-type zinc finger 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1552290	Flywch1	FLYWCH-type zinc finger 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552290	Flywch1	FLYWCH-type zinc finger 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20200402	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101104
1552292	E2f6	E2F transcription factor 6	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15936277
1552292	E2f6	E2F transcription factor 6	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101104
1552292	E2f6	E2F transcription factor 6	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20260402	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101104
1552292	E2f6	E2F transcription factor 6	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12101104
1552292	E2f6	E2F transcription factor 6	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20260402	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18366140
1552292	E2f6	E2F transcription factor 6	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20250508	MGI			
1552292	E2f6	E2F transcription factor 6	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20250508	MGI			
1552295	Epha8	Eph receptor A8	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9214628
1552295	Epha8	Eph receptor A8	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9214628
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0004757	abnormal distal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005502	abnormal renal/urinary system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008137	absent podocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0011428	decreased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498891
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0014350	disorganized spleen B cell follicle		IAGP		N	RGD:5509061	20240104	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0014471	enhanced B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:17142749
1552296	Arhgdia	Rho GDP dissociation inhibitor alpha	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:10498891
1552297	Col14a1	collagen, type XIV, alpha 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136672
1552297	Col14a1	collagen, type XIV, alpha 1	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136672
1552297	Col14a1	collagen, type XIV, alpha 1	gene	MP:0003098	decreased tendon stiffness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136672
1552297	Col14a1	collagen, type XIV, alpha 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1552297	Col14a1	collagen, type XIV, alpha 1	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136672
1552299	Tspan4	tetraspanin 4	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240613	MGI			PMID:38786026
1552302	Hdac6	histone deacetylase 6	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180281
1552302	Hdac6	histone deacetylase 6	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364049
1552302	Hdac6	histone deacetylase 6	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180281
1552302	Hdac6	histone deacetylase 6	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180281
1552302	Hdac6	histone deacetylase 6	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180281
1552302	Hdac6	histone deacetylase 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180281
1552302	Hdac6	histone deacetylase 6	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20151112	MGI			PMID:17938201
1552302	Hdac6	histone deacetylase 6	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20160929	MGI			PMID:23184605
1552302	Hdac6	histone deacetylase 6	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364049
1552302	Hdac6	histone deacetylase 6	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20160929	MGI			PMID:23184605
1552302	Hdac6	histone deacetylase 6	gene	MP:0008594	decreased circulating interleukin-10 level		IAGP		N	RGD:5509061	20160225	MGI			PMID:24747960
1552302	Hdac6	histone deacetylase 6	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20160225	MGI			PMID:24747960
1552302	Hdac6	histone deacetylase 6	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364049
1552302	Hdac6	histone deacetylase 6	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364049
1552302	Hdac6	histone deacetylase 6	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:18180281
1552302	Hdac6	histone deacetylase 6	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364049
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20220203	MGI			PMID:30355948
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0004941	abnormal regulatory T cell morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:30355948
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20220203	MGI			PMID:30355948
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20220203	MGI			PMID:30355948
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20220203	MGI			PMID:30355948
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20220203	MGI			PMID:30355948
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0008629	increased circulating interleukin-9 level		IAGP		N	RGD:5509061	20220203	MGI			PMID:30355948
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20220203	MGI			PMID:30355948
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20260402	MGI			
1552303	Colgalt2	collagen beta(1-O)galactosyltransferase 2	gene	MP:0012773	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20220203	MGI			PMID:30355948
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0000467	abnormal esophagus morphology		IEA		N	RGD:5509061	20200402	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20170105	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20170105	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20200402	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20190502	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230601	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20200402	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20170105	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20201022	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0012188	increased regulatory T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20241121	MGI			
1552304	Itch	itchy, E3 ubiquitin protein ligase	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479951
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20260402	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479951
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479951
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217325
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479951
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0008180	abnormal marginal zone B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19217325
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479951
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230601	MGI			
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479951
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0012355	decreased prothrombin time		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0012358	decreased partial thromboplastin time		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0012616	increased circulating factor IX level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1552305	Mfng	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	gene	MP:0020985	increased circulating factor XI level		IAGP		N	RGD:5509061	20210204	MGI			PMID:23118208
1552306	Prpf31	pre-mRNA processing factor 31	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811066
1552306	Prpf31	pre-mRNA processing factor 31	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1552306	Prpf31	pre-mRNA processing factor 31	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811066
1552306	Prpf31	pre-mRNA processing factor 31	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1552306	Prpf31	pre-mRNA processing factor 31	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578015
1552306	Prpf31	pre-mRNA processing factor 31	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19578015
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:29419376
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29419376
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0003247	abnormal glutaminergic neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29419376
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:40393451
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0010167	decreased response to stress-induced hyperthermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29419376
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0011002	enhanced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:29419376
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20260507	MGI			PMID:40393451
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:29419376
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0014413	decreased depression-related behavior		IAGP		N	RGD:5509061	20240425	MGI			PMID:29419376
1552307	Gpr158	G protein-coupled receptor 158	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20200310	MGI			PMID:29419376
1552308	Wdr76	WD repeat domain 76	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:30655611
1552311	Cdh15	cadherin 15	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12052883
1552312	Peli3	pellino 3	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23042151
1552312	Peli3	pellino 3	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20200310	MGI			
1552312	Peli3	pellino 3	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20200310	MGI			
1552312	Peli3	pellino 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23042151
1552312	Peli3	pellino 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1552312	Peli3	pellino 3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1552312	Peli3	pellino 3	gene	MP:0011072	abnormal macrophage cytokine production		IAGP		N	RGD:5509061	20200310	MGI			PMID:23042151
1552312	Peli3	pellino 3	gene	MP:0020938	decreased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23042151
1552312	Peli3	pellino 3	gene	MP:0031039	decreased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:23042151
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0003402	decreased liver weight		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20170713	MGI			PMID:28655767
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0013514	increased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0013520	increased CD4-positive NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1552314	Mettl6	methyltransferase 6, methylcytidine	gene	MP:0013523	increased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1552316	Taar3	trace amine-associated receptor 3	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20210520	MGI			
1552316	Taar3	trace amine-associated receptor 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20241121	MGI			
1552316	Taar3	trace amine-associated receptor 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220811	MGI			
1552316	Taar3	trace amine-associated receptor 3	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210520	MGI			
1552316	Taar3	trace amine-associated receptor 3	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20241121	MGI			
1552316	Taar3	trace amine-associated receptor 3	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20220811	MGI			
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0008089	abnormal T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0008091	decreased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0008723	impaired eosinophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0008769	abnormal plasmacytoid dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552317	Chi3l1	chitinase 3 like 1	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19414556
1552322	Cstf3	cleavage stimulation factor, 3' pre-RNA, subunit 3	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20190502	MGI			
1552322	Cstf3	cleavage stimulation factor, 3' pre-RNA, subunit 3	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20190502	MGI			
1552322	Cstf3	cleavage stimulation factor, 3' pre-RNA, subunit 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20190502	MGI			
1552322	Cstf3	cleavage stimulation factor, 3' pre-RNA, subunit 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1552322	Cstf3	cleavage stimulation factor, 3' pre-RNA, subunit 3	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
1552322	Cstf3	cleavage stimulation factor, 3' pre-RNA, subunit 3	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1552322	Cstf3	cleavage stimulation factor, 3' pre-RNA, subunit 3	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1552322	Cstf3	cleavage stimulation factor, 3' pre-RNA, subunit 3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1552322	Cstf3	cleavage stimulation factor, 3' pre-RNA, subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1552325	Ublcp1	ubiquitin-like domain containing CTD phosphatase 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20200310	MGI			
1552325	Ublcp1	ubiquitin-like domain containing CTD phosphatase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1552325	Ublcp1	ubiquitin-like domain containing CTD phosphatase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552326	Tacc2	transforming, acidic coiled-coil containing protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226440
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0000263	absent organized vascular network		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360632
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360632
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360632
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360632
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360632
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20260402	MGI			
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360632
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360632
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20260402	MGI			
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360632
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0012254	absent intersomitic vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514057
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0012270	cardiac edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21559415
1552328	Ptprb	protein tyrosine phosphatase receptor type B	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1552329	Arf5	ARF GTPase 5	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20191114	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0014621	abnormal brain alpha wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0014622	abnormal brain beta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:31201232
1552329	Arf5	ARF GTPase 5	gene	MP:0014624	abnormal brain delta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:31201232
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:2055457
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:2693209
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20200310	MGI			PMID:29720471
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20200310	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:2693209
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0014958	decreased lung enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0014966	decreased heart enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0014972	decreased spleen enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19220926
1552331	Tpi1	triosephosphate isomerase 1	gene	MP:0014975	decreased kidney enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:19220926
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20181227	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191205	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20181227	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200409	MGI			PMID:29479578
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200409	MGI			PMID:29479578
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20191205	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1552332	Ap2s1	adaptor-related protein complex 2, sigma 1 subunit	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241128	MGI			
1552333	Cnksr2	connector enhancer of kinase suppressor of Ras 2	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1552333	Cnksr2	connector enhancer of kinase suppressor of Ras 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220519	MGI			
1552333	Cnksr2	connector enhancer of kinase suppressor of Ras 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1552334	Rhot2	ras homolog family member T2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1552334	Rhot2	ras homolog family member T2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170817	MGI			PMID:27705781
1552334	Rhot2	ras homolog family member T2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1552334	Rhot2	ras homolog family member T2	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20160804	MGI			
1552334	Rhot2	ras homolog family member T2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160804	MGI			
1552336	Msh5	mutS homolog 5	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1552336	Msh5	mutS homolog 5	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1552336	Msh5	mutS homolog 5	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072381
1552336	Msh5	mutS homolog 5	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20220421	MGI			PMID:28175301
1552336	Msh5	mutS homolog 5	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20220811	MGI			
1552336	Msh5	mutS homolog 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072381
1552336	Msh5	mutS homolog 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1552336	Msh5	mutS homolog 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072381
1552336	Msh5	mutS homolog 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1552336	Msh5	mutS homolog 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220421	MGI			PMID:28175301
1552336	Msh5	mutS homolog 5	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141120	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072381
1552336	Msh5	mutS homolog 5	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072381
1552336	Msh5	mutS homolog 5	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20220421	MGI			PMID:28175301
1552336	Msh5	mutS homolog 5	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20220421	MGI			PMID:28175301
1552336	Msh5	mutS homolog 5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072381
1552336	Msh5	mutS homolog 5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072381
1552336	Msh5	mutS homolog 5	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072381
1552336	Msh5	mutS homolog 5	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10809667
1552336	Msh5	mutS homolog 5	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10072381
1552336	Msh5	mutS homolog 5	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20220623	MGI			PMID:21915857
1552336	Msh5	mutS homolog 5	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20180111	MGI			PMID:21915857
1552336	Msh5	mutS homolog 5	gene	MP:0013236	ovary degeneration		IAGP		N	RGD:5509061	20141120	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0013605	abnormal ovarian bursa morphology		IAGP		N	RGD:5509061	20150312	MGI			PMID:9916805
1552336	Msh5	mutS homolog 5	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:10072381
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0005386	behavior/neurological phenotype		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0012006	abnormal hippocampus physiology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0020520	whitened brown adipose tissue morphology		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0031271	increased susceptibility to age-related hepatic steatosis		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552339	Saraf	store-operated calcium entry-associated regulatory factor	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20231019	MGI			PMID:37007714
1552341	Ttc1	tetratricopeptide repeat domain 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210826	MGI			
1552341	Ttc1	tetratricopeptide repeat domain 1	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241003	MGI			
1552341	Ttc1	tetratricopeptide repeat domain 1	gene	MP:0002718	abnormal inner cell mass morphology		IEA		N	RGD:5509061	20241003	MGI			
1552341	Ttc1	tetratricopeptide repeat domain 1	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20210520	MGI			
1552341	Ttc1	tetratricopeptide repeat domain 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1552341	Ttc1	tetratricopeptide repeat domain 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1552341	Ttc1	tetratricopeptide repeat domain 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241003	MGI			
1552342	Cd302	CD302 antigen	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20210805	MGI			PMID:27316686
1552342	Cd302	CD302 antigen	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20210805	MGI			PMID:27316686
1552342	Cd302	CD302 antigen	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20210805	MGI			PMID:27316686
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000495	abnormal colon morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002759	abnormal caudal vertebrae morphology		IEA		N	RGD:5509061	20230601	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002981	increased liver weight		IEA		N	RGD:5509061	20231207	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20231207	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20231207	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0009483	enlarged ileum		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210520	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20231207	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0011080	increased macrophage apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22174130
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0011503	distended jejunum		IEA		N	RGD:5509061	20230119	MGI			
1552344	Slc29a3	solute carrier family 29 (nucleoside transporters), member 3	gene	MP:0011882	enlarged duodenum		IEA		N	RGD:5509061	20230119	MGI			
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0001553	abnormal circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18499755
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19865172
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160602	MGI			PMID:25581519
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19865172
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19865172
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0002467	impaired neutrophil phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19865172
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20160602	MGI			PMID:25581519
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22190648
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0003564	abnormal insulin secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25581519
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19865172
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19865172
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0005044	sepsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20160602	MGI			PMID:25581519
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22190648
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19865172
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19865172
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19865172
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917676
1552346	Ffar2	free fatty acid receptor 2	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22190648
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767743
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767743
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767743
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767743
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767743
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767743
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767743
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767743
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:19767743
1552347	Creb3l1	cAMP responsive element binding protein 3-like 1	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:19767743
1552349	Rhbg	Rh family B glycoprotein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16077082
1552349	Rhbg	Rh family B glycoprotein	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20201022	MGI			
1552349	Rhbg	Rh family B glycoprotein	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1552349	Rhbg	Rh family B glycoprotein	gene	MP:0011736	decreased urine ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20719974
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20221215	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1552350	Ankmy2	ankyrin repeat and MYND domain containing 2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220811	MGI			
1552352	Dck	deoxycytidine kinase	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0001606	impaired hematopoiesis		IEA		N	RGD:5509061	20161201	MGI			
1552352	Dck	deoxycytidine kinase	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20161201	MGI			
1552352	Dck	deoxycytidine kinase	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1552352	Dck	deoxycytidine kinase	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0002497	increased IgE level		IEA		N	RGD:5509061	20161201	MGI			
1552352	Dck	deoxycytidine kinase	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0005046	absent spleen white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0005425	increased macrophage cell number		IEA		N	RGD:5509061	20161201	MGI			
1552352	Dck	deoxycytidine kinase	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20161201	MGI			
1552352	Dck	deoxycytidine kinase	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080663
1552352	Dck	deoxycytidine kinase	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407915
1552352	Dck	deoxycytidine kinase	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20161201	MGI			
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16880526
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16880526
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16880526
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16880526
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16880526
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20200310	MGI			
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20200310	MGI			
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16880526
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17998335
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16880526
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16880526
1552356	Fbxw8	F-box and WD-40 domain protein 8	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552359	Usp13	ubiquitin specific peptidase 13 (isopeptidase T-3)	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200521	MGI			PMID:31204278
1552359	Usp13	ubiquitin specific peptidase 13 (isopeptidase T-3)	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200521	MGI			PMID:31204278
1552359	Usp13	ubiquitin specific peptidase 13 (isopeptidase T-3)	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1552359	Usp13	ubiquitin specific peptidase 13 (isopeptidase T-3)	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200521	MGI			PMID:31204278
1552359	Usp13	ubiquitin specific peptidase 13 (isopeptidase T-3)	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200521	MGI			PMID:31204278
1552359	Usp13	ubiquitin specific peptidase 13 (isopeptidase T-3)	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20200521	MGI			PMID:31204278
1552359	Usp13	ubiquitin specific peptidase 13 (isopeptidase T-3)	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1552363	Cd276	CD276 antigen	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1552363	Cd276	CD276 antigen	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925852
1552363	Cd276	CD276 antigen	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1552363	Cd276	CD276 antigen	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15682454
1552363	Cd276	CD276 antigen	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20170209	MGI			PMID:26065426
1552363	Cd276	CD276 antigen	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925852
1552363	Cd276	CD276 antigen	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925852
1552363	Cd276	CD276 antigen	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20170209	MGI			PMID:26065426
1552363	Cd276	CD276 antigen	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925852
1552363	Cd276	CD276 antigen	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925852
1552363	Cd276	CD276 antigen	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:26065426
1552363	Cd276	CD276 antigen	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:26065426
1552363	Cd276	CD276 antigen	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1552363	Cd276	CD276 antigen	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20170209	MGI			PMID:26065426
1552363	Cd276	CD276 antigen	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:15682454
1552363	Cd276	CD276 antigen	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925852
1552363	Cd276	CD276 antigen	gene	MP:0010222	abnormal T-helper 17 cell physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:26065426
1552365	Cdk9	cyclin dependent kinase 9	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20220519	MGI			
1552365	Cdk9	cyclin dependent kinase 9	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1552365	Cdk9	cyclin dependent kinase 9	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20170105	MGI			
1552365	Cdk9	cyclin dependent kinase 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552365	Cdk9	cyclin dependent kinase 9	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552365	Cdk9	cyclin dependent kinase 9	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:12384239
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12384239
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:11752130
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12384239
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0001486	abnormal startle reflex		IAGP		N	RGD:5509061	20200310	MGI			PMID:19596359
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20200310	MGI			PMID:19596359
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19223157
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15030383
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:11752130
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:14725975
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19223157
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0002733	abnormal thermal nociception		IAGP		N	RGD:5509061	20200310	MGI			PMID:19223157
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20200310	MGI			PMID:19596359
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0003290	intestinal hypoperistalsis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11752130
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20200310	MGI			PMID:12384239
1552366	Ntsr1	neurotensin receptor 1	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20200310	MGI			PMID:11752130
1552367	Wbp2	WW domain binding protein 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20170202	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1552367	Wbp2	WW domain binding protein 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1552367	Wbp2	WW domain binding protein 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160804	MGI			
1552367	Wbp2	WW domain binding protein 2	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20170202	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20170202	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0004746	abnormal cochlear IHC afferent innervation pattern		IAGP		N	RGD:5509061	20170202	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0004747	abnormal cochlear OHC afferent innervation pattern		IAGP		N	RGD:5509061	20170202	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1552367	Wbp2	WW domain binding protein 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160804	MGI			
1552367	Wbp2	WW domain binding protein 2	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20160804	MGI			
1552367	Wbp2	WW domain binding protein 2	gene	MP:0006388	abnormal auditory summating potential		IAGP		N	RGD:5509061	20170202	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0008805	decreased circulating amylase level		IAGP		N	RGD:5509061	20170202	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20160804	MGI			
1552367	Wbp2	WW domain binding protein 2	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20170202	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20170202	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0014740	increased auditory brainstem response wave peak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:26881968
1552367	Wbp2	WW domain binding protein 2	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:26881968
1552368	Cyb561d2	cytochrome b-561 domain containing 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1552368	Cyb561d2	cytochrome b-561 domain containing 2	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20250508	MGI			
1552368	Cyb561d2	cytochrome b-561 domain containing 2	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1552370	Tpbg	trophoblast glycoprotein	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20376365
1552370	Tpbg	trophoblast glycoprotein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20376365
1552370	Tpbg	trophoblast glycoprotein	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507657
1552370	Tpbg	trophoblast glycoprotein	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20376365
1552370	Tpbg	trophoblast glycoprotein	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507657
1552372	Hace1	HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17694067
1552372	Hace1	HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17694067
1552372	Hace1	HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17694067
1552372	Hace1	HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552372	Hace1	HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0000954	decreased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0012066	decreased astrocyte number		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552374	Prrc2a	proline-rich coiled-coil 2A	gene	MP:0013438	dysmyelination		IAGP		N	RGD:5509061	20210805	MGI			PMID:30514900
1552380	Podxl2	podocalyxin-like 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552380	Podxl2	podocalyxin-like 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20200310	MGI			
1552380	Podxl2	podocalyxin-like 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20200310	MGI			
1552380	Podxl2	podocalyxin-like 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200310	MGI			
1552380	Podxl2	podocalyxin-like 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210603	MGI			PMID:27542690
1552383	Chst7	carbohydrate sulfotransferase 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191017	MGI			PMID:30867513
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0010578	abnormal heart left ventricle size		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20220120	MGI			PMID:31721250
1552385	Mrps12	mitochondrial ribosomal protein S12	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:31721250
1552386	Tlr6	toll-like receptor 6	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1552386	Tlr6	toll-like receptor 6	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1552386	Tlr6	toll-like receptor 6	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1552386	Tlr6	toll-like receptor 6	gene	MP:0002421	abnormal cell-mediated immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1552386	Tlr6	toll-like receptor 6	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1552386	Tlr6	toll-like receptor 6	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16832055
1552386	Tlr6	toll-like receptor 6	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1552386	Tlr6	toll-like receptor 6	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1552386	Tlr6	toll-like receptor 6	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1552386	Tlr6	toll-like receptor 6	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431423
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16103361
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:16103361
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17210641
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0002310	decreased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24567531
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17210641
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24567531
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17210641
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24567531
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17210641
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24567531
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717184
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17210641
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16103361
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:24567531
1552388	Acaca	acetyl-Coenzyme A carboxylase alpha	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:16717184
1552392	Zfp629	zinc finger protein 629	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220519	MGI			
1552392	Zfp629	zinc finger protein 629	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1552392	Zfp629	zinc finger protein 629	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1552392	Zfp629	zinc finger protein 629	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1552392	Zfp629	zinc finger protein 629	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1552396	Slc30a3	solute carrier family 30 (zinc transporter), member 3	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990090
1552396	Slc30a3	solute carrier family 30 (zinc transporter), member 3	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032347
1552396	Slc30a3	solute carrier family 30 (zinc transporter), member 3	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990090
1552396	Slc30a3	solute carrier family 30 (zinc transporter), member 3	gene	MP:0009615	abnormal zinc homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990090
1552396	Slc30a3	solute carrier family 30 (zinc transporter), member 3	gene	MP:0009617	decreased brain zinc level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032347
1552396	Slc30a3	solute carrier family 30 (zinc transporter), member 3	gene	MP:0009617	decreased brain zinc level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990090
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0001432	abnormal food preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742914
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16299503
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0001981	increased chemically-elicited antinociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:16299503
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742914
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16299503
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:16299503
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742914
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:14742914
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0009713	enhanced conditioned place preference behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16299503
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0009776	decreased behavioral withdrawal response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16299503
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552398	Prlhr	prolactin releasing hormone receptor	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904108
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305243
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305243
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056377
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056377
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305243
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305243
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056377
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382154
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305243
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0004494	abnormal synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:18305243
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382154
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18625726
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16382154
1552399	Rap1a	Rap1a member of RAS oncogene family	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056377
1552400	Notch3	notch 3	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552400	Notch3	notch 3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1552400	Notch3	notch 3	gene	MP:0000262	poor arterial differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545631
1552400	Notch3	notch 3	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
1552400	Notch3	notch 3	gene	MP:0000648	absent sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
1552400	Notch3	notch 3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1552400	Notch3	notch 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1552400	Notch3	notch 3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882997
1552400	Notch3	notch 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882997
1552400	Notch3	notch 3	gene	MP:0000751	myopathy		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21940951
1552400	Notch3	notch 3	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897741
1552400	Notch3	notch 3	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
1552400	Notch3	notch 3	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525534
1552400	Notch3	notch 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21940951
1552400	Notch3	notch 3	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21940951
1552400	Notch3	notch 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595837
1552400	Notch3	notch 3	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1552400	Notch3	notch 3	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:21940951
1552400	Notch3	notch 3	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595837
1552400	Notch3	notch 3	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595837
1552400	Notch3	notch 3	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1552400	Notch3	notch 3	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545631
1552400	Notch3	notch 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1552400	Notch3	notch 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595837
1552400	Notch3	notch 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15645445
1552400	Notch3	notch 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991352
1552400	Notch3	notch 3	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21940951
1552400	Notch3	notch 3	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545631
1552400	Notch3	notch 3	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21940951
1552400	Notch3	notch 3	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
1552400	Notch3	notch 3	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1552400	Notch3	notch 3	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
1552400	Notch3	notch 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20170105	MGI			
1552400	Notch3	notch 3	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347334
1552400	Notch3	notch 3	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555590
1552400	Notch3	notch 3	gene	MP:0003402	decreased liver weight		IEA		N	RGD:5509061	20210128	MGI			
1552400	Notch3	notch 3	gene	MP:0003554	phimosis		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
1552400	Notch3	notch 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595837
1552400	Notch3	notch 3	gene	MP:0004125	abnormal venule morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
1552400	Notch3	notch 3	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1552400	Notch3	notch 3	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0005150	cachexia		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20160211	MGI			
1552400	Notch3	notch 3	gene	MP:0005532	abnormal vascular resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545631
1552400	Notch3	notch 3	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15545631
1552400	Notch3	notch 3	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555590
1552400	Notch3	notch 3	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
1552400	Notch3	notch 3	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897741
1552400	Notch3	notch 3	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347334
1552400	Notch3	notch 3	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347334
1552400	Notch3	notch 3	gene	MP:0006093	arteriovenous malformation		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
1552400	Notch3	notch 3	gene	MP:0006325	impaired hearing		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1552400	Notch3	notch 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1552400	Notch3	notch 3	gene	MP:0009417	skeletal muscle atrophy		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0009661	abnormal pregnancy		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347334
1552400	Notch3	notch 3	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1552400	Notch3	notch 3	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
1552400	Notch3	notch 3	gene	MP:0010174	decreased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24100291
1552400	Notch3	notch 3	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897741
1552400	Notch3	notch 3	gene	MP:0011181	increased hematopoietic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21562564
1552400	Notch3	notch 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20141003	MGI			
1552400	Notch3	notch 3	gene	MP:0013925	abnormal vascular plexus formation		IAGP		N	RGD:5509061	20160609	MGI			PMID:26563570
1552400	Notch3	notch 3	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:21940951
1552400	Notch3	notch 3	gene	MP:0030438	increased osteoblast proliferation		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0030482	increased osteocyte number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30042232
1552400	Notch3	notch 3	gene	MP:0031168	abnormal brain thrombosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:21940951
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10798394
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186781
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537788
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353676
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147989
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21613506
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035080
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0001983	abnormal olfactory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10798394
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0001984	abnormal olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186782
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19186165
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186782
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186782
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147989
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186782
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10798394
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537788
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10798394
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17521568
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147989
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035080
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646512
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147989
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147989
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0010057	abnormal olfactory bulb outer nerve layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21147989
1552401	Or8a1b	olfactory receptor family 8 subfamily A member 1B	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186781
1552402	Cldn18	claudin 18	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1552402	Cldn18	claudin 18	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20181227	MGI			
1552402	Cldn18	claudin 18	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0004882	enlarged lung		IEA		N	RGD:5509061	20210128	MGI			
1552402	Cldn18	claudin 18	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0005630	increased lung weight		IEA		N	RGD:5509061	20201022	MGI			
1552402	Cldn18	claudin 18	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20160707	MGI			PMID:24787463
1552402	Cldn18	claudin 18	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1552402	Cldn18	claudin 18	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20160707	MGI			PMID:24787463
1552402	Cldn18	claudin 18	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552402	Cldn18	claudin 18	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:24787463
1552402	Cldn18	claudin 18	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:24787463
1552402	Cldn18	claudin 18	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23299504
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658157
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:20956301
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658157
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19718039
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658157
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0009959	abnormal cerebellar hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081859
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623382
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0013202	abnormal cilium morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:19625297
1552406	Ahi1	Abelson helper integration site 1	gene	MP:0013305	isosthenuria		IAGP		N	RGD:5509061	20141120	MGI			PMID:19718039
1552408	Eomes	eomesodermin	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1552408	Eomes	eomesodermin	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077589
1552408	Eomes	eomesodermin	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0001357	increased aggression towards humans		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20220421	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716450
1552408	Eomes	eomesodermin	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19830823
1552408	Eomes	eomesodermin	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0001714	absent trophoblast giant cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788452
1552408	Eomes	eomesodermin	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788452
1552408	Eomes	eomesodermin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716450
1552408	Eomes	eomesodermin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788452
1552408	Eomes	eomesodermin	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1552408	Eomes	eomesodermin	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1552408	Eomes	eomesodermin	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077589
1552408	Eomes	eomesodermin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897762
1552408	Eomes	eomesodermin	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19830823
1552408	Eomes	eomesodermin	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1552408	Eomes	eomesodermin	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0003085	abnormal egg cylinder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716450
1552408	Eomes	eomesodermin	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1552408	Eomes	eomesodermin	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19830823
1552408	Eomes	eomesodermin	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1552408	Eomes	eomesodermin	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716450
1552408	Eomes	eomesodermin	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1552408	Eomes	eomesodermin	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077589
1552408	Eomes	eomesodermin	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1552408	Eomes	eomesodermin	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1552408	Eomes	eomesodermin	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1552408	Eomes	eomesodermin	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1552408	Eomes	eomesodermin	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1552408	Eomes	eomesodermin	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1552408	Eomes	eomesodermin	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20151231	MGI			PMID:24516120
1552408	Eomes	eomesodermin	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077589
1552408	Eomes	eomesodermin	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1552408	Eomes	eomesodermin	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1552408	Eomes	eomesodermin	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1552408	Eomes	eomesodermin	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1552408	Eomes	eomesodermin	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0008507	thin retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077589
1552408	Eomes	eomesodermin	gene	MP:0008530	abnormal rostral-caudal patterning of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16273099
1552408	Eomes	eomesodermin	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1552408	Eomes	eomesodermin	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1552408	Eomes	eomesodermin	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713880
1552408	Eomes	eomesodermin	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18635804
1552408	Eomes	eomesodermin	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716450
1552408	Eomes	eomesodermin	gene	MP:0009850	embryonic lethality between implantation and placentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23897762
1552408	Eomes	eomesodermin	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1552408	Eomes	eomesodermin	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1552408	Eomes	eomesodermin	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788452
1552408	Eomes	eomesodermin	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19830823
1552408	Eomes	eomesodermin	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716450
1552408	Eomes	eomesodermin	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552408	Eomes	eomesodermin	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0011255	abnormal anterior visceral endoderm cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0012102	absent trophectoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15788452
1552408	Eomes	eomesodermin	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0012156	rostral-caudal axis duplication		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0012181	increased somite number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18171685
1552408	Eomes	eomesodermin	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716450
1552408	Eomes	eomesodermin	gene	MP:0012739	abnormal anterior primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10716450
1552408	Eomes	eomesodermin	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552408	Eomes	eomesodermin	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552408	Eomes	eomesodermin	gene	MP:0014751	abnormal commissural neuron axon guidance		IAGP		N	RGD:5509061	20250904	MGI			PMID:18794345
1552408	Eomes	eomesodermin	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18635804
1552408	Eomes	eomesodermin	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:18077589
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0001819	abnormal immune cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11489994
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11086056
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11489994
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0008879	submandibular gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0010286	increased plasmacytoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081683
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11086056
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15039466
1552409	Il12rb2	interleukin 12 receptor, beta 2	gene	MP:0013367	parotid gland inflammation		IAGP		N	RGD:5509061	20141225	MGI			PMID:16081683
1552410	Gcnt2	glucosaminyl (N-acetyl) transferase 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107727
1552410	Gcnt2	glucosaminyl (N-acetyl) transferase 2	gene	MP:0002015	epithelioid cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107727
1552410	Gcnt2	glucosaminyl (N-acetyl) transferase 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107727
1552410	Gcnt2	glucosaminyl (N-acetyl) transferase 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107727
1552410	Gcnt2	glucosaminyl (N-acetyl) transferase 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107727
1552410	Gcnt2	glucosaminyl (N-acetyl) transferase 2	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16107727
1552411	Rpusd2	RNA pseudouridylate synthase domain containing 2	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1552411	Rpusd2	RNA pseudouridylate synthase domain containing 2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20201022	MGI			
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305608
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000064	failure of bone resorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:3976544
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305608
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3976544
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:3976544
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20241121	MGI			
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20241121	MGI			
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000576	clubfoot		IEA		N	RGD:5509061	20111116	MGI			
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10709991
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549681
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10709991
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305608
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549681
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549681
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002360	abnormal spleen B cell corona morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19549681
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046993
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0003053	delayed tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:10709991
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0003053	delayed tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17046993
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:3976544
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20241121	MGI			
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305608
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305608
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:3976544
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0008271	abnormal bone ossification		IEA		N	RGD:5509061	20111116	MGI			
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20260402	MGI			
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305608
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21305608
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0010969	absent compact bone		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0012336	decreased vitamin D level		IAGP		N	RGD:5509061	20151112	MGI			PMID:25811986
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0014348	decreased spleen B cell follicle size		IAGP		N	RGD:5509061	20240104	MGI			PMID:15294947
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0030543	abnormal predentin morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:3998439
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20180726	MGI			PMID:10581033
1552412	Tcirg1	T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20180726	MGI			PMID:19549681
1552413	Pde8b	phosphodiesterase 8B	gene	MP:0002664	decreased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21187369
1552413	Pde8b	phosphodiesterase 8B	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21187369
1552413	Pde8b	phosphodiesterase 8B	gene	MP:0011549	increased urine corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21187369
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0001793	abnormal susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426143
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0008244	abnormal peritoneal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7884909
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:7884909
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:7769712
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:7884909
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:7769712
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:7884909
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0031023	decreased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:7769712
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0031045	decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:7769712
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0031045	decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:7884909
1552414	Mx1	MX dynamin-like GTPase 1	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:7884909
1552415	Sgtb	small glutamine-rich tetratricopeptide repeat (TPR)-containing, beta	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1552418	Krt15	keratin 15	gene	MP:0000466	esophageal epithelium hyperplasia		IAGP		N	RGD:5509061	20180315	MGI			PMID:28481227
1552418	Krt15	keratin 15	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20180315	MGI			PMID:28481227
1552418	Krt15	keratin 15	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20180315	MGI			PMID:28481227
1552419	Map2k6	mitogen-activated protein kinase kinase 6	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151339
1552419	Map2k6	mitogen-activated protein kinase kinase 6	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12824301
1552419	Map2k6	mitogen-activated protein kinase kinase 6	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:12824301
1552419	Map2k6	mitogen-activated protein kinase kinase 6	gene	MP:0009258	abnormal thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151339
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220811	MGI			
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002414	abnormal myeloblast morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20221215	MGI			
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0003121	genetic imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18728284
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0008878	abnormal DNA methylation during gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0009257	dilated seminiferous tubule		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200402	MGI			
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043311
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20170803	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:26258622
1552420	Arid4b	AT-rich interaction domain 4B	gene	MP:0031070	hemophagocytosis		IAGP		N	RGD:5509061	20200618	MGI			PMID:18728284
1552421	Rab35	RAB35, member RAS oncogene family	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20200310	MGI			
1552421	Rab35	RAB35, member RAS oncogene family	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20200310	MGI			
1552421	Rab35	RAB35, member RAS oncogene family	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552421	Rab35	RAB35, member RAS oncogene family	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20201029	MGI			PMID:32503983
1552421	Rab35	RAB35, member RAS oncogene family	gene	MP:0012674	tomacula		IAGP		N	RGD:5509061	20201029	MGI			PMID:32503983
1552421	Rab35	RAB35, member RAS oncogene family	gene	MP:0020434	increased astrocyte size		IAGP		N	RGD:5509061	20201029	MGI			PMID:32503983
1552422	Cfap20dc	CFAP20 domain containing	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1552422	Cfap20dc	CFAP20 domain containing	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20240523	MGI			
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843402
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20150702	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791266
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843402
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791266
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12843402
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791266
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791266
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791266
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12791266
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20150212	MGI			PMID:12843402
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:12843402
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:12791266
1552424	Btrc	beta-transducin repeat containing protein	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:24469832
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7891151
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7891151
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3678603
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:3678603
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:20041218
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210520	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20041218
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20041218
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20041218
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20041218
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20220811	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210520	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0013022	increased Ly6C high monocyte number		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0013025	increased Ly6C low monocyte number		IEA		N	RGD:5509061	20181227	MGI			
1552425	Herc1	HECT and RLD domain containing E3 ubiquitin protein ligase family member 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1552429	Cept1	choline/ethanolaminephosphotransferase 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20180322	MGI			PMID:26512026
1552429	Cept1	choline/ethanolaminephosphotransferase 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20180322	MGI			PMID:26512026
1552429	Cept1	choline/ethanolaminephosphotransferase 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20180322	MGI			PMID:26512026
1552429	Cept1	choline/ethanolaminephosphotransferase 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20180322	MGI			PMID:26512026
1552429	Cept1	choline/ethanolaminephosphotransferase 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20180322	MGI			PMID:26512026
1552429	Cept1	choline/ethanolaminephosphotransferase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20180322	MGI			PMID:26512026
1552429	Cept1	choline/ethanolaminephosphotransferase 1	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20180322	MGI			PMID:26512026
1552429	Cept1	choline/ethanolaminephosphotransferase 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20180322	MGI			PMID:26512026
1552430	Clock	clock circadian regulator	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629164
1552430	Clock	clock circadian regulator	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16879220
1552430	Clock	clock circadian regulator	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12882315
1552430	Clock	clock circadian regulator	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15967985
1552430	Clock	clock circadian regulator	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732766
1552430	Clock	clock circadian regulator	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15967985
1552430	Clock	clock circadian regulator	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12882315
1552430	Clock	clock circadian regulator	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732766
1552430	Clock	clock circadian regulator	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11050136
1552430	Clock	clock circadian regulator	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11388430
1552430	Clock	clock circadian regulator	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16879220
1552430	Clock	clock circadian regulator	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16879220
1552430	Clock	clock circadian regulator	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562852
1552430	Clock	clock circadian regulator	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19387090
1552430	Clock	clock circadian regulator	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15523558
1552430	Clock	clock circadian regulator	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16879220
1552430	Clock	clock circadian regulator	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15523558
1552430	Clock	clock circadian regulator	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21123577
1552430	Clock	clock circadian regulator	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20240627	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12882315
1552430	Clock	clock circadian regulator	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15967985
1552430	Clock	clock circadian regulator	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16732766
1552430	Clock	clock circadian regulator	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562852
1552430	Clock	clock circadian regulator	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16879220
1552430	Clock	clock circadian regulator	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15523558
1552430	Clock	clock circadian regulator	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562852
1552430	Clock	clock circadian regulator	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562852
1552430	Clock	clock circadian regulator	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15967985
1552430	Clock	clock circadian regulator	gene	MP:0003969	abnormal luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0004080	abnormal nucleus accumbens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21123577
1552430	Clock	clock circadian regulator	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12882315
1552430	Clock	clock circadian regulator	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413500
1552430	Clock	clock circadian regulator	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16879220
1552430	Clock	clock circadian regulator	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0005186	increased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562852
1552430	Clock	clock circadian regulator	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562852
1552430	Clock	clock circadian regulator	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562852
1552430	Clock	clock circadian regulator	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360665
1552430	Clock	clock circadian regulator	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19387090
1552430	Clock	clock circadian regulator	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18413500
1552430	Clock	clock circadian regulator	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16879220
1552430	Clock	clock circadian regulator	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16879220
1552430	Clock	clock circadian regulator	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16879220
1552430	Clock	clock circadian regulator	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0008462	abnormal medium spiny neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21123577
1552430	Clock	clock circadian regulator	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:19629164
1552430	Clock	clock circadian regulator	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18007188
1552430	Clock	clock circadian regulator	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19387090
1552430	Clock	clock circadian regulator	gene	MP:0008961	abnormal basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0009015	short proestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562852
1552430	Clock	clock circadian regulator	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15296754
1552430	Clock	clock circadian regulator	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:15967985
1552430	Clock	clock circadian regulator	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0010896	decreased lung compliance		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11388430
1552430	Clock	clock circadian regulator	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20171012	MGI			PMID:16732766
1552430	Clock	clock circadian regulator	gene	MP:0011021	abnormal circadian regulation of heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360665
1552430	Clock	clock circadian regulator	gene	MP:0011022	abnormal circadian regulation of systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360665
1552430	Clock	clock circadian regulator	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20241121	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0013758	increased intestinal glucose absorption		IAGP		N	RGD:5509061	20191031	MGI			PMID:19387090
1552430	Clock	clock circadian regulator	gene	MP:0013763	increased T-helper cell number		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20230601	MGI			
1552430	Clock	clock circadian regulator	gene	MP:0014121	increased pancreatic islet cell apoptosis		IAGP		N	RGD:5509061	20160324	MGI			PMID:20562852
1552430	Clock	clock circadian regulator	gene	MP:0014639	decreased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:11050136
1552430	Clock	clock circadian regulator	gene	MP:0014639	decreased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:11388430
1552430	Clock	clock circadian regulator	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:11050136
1552430	Clock	clock circadian regulator	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:11388430
1552430	Clock	clock circadian regulator	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:16732766
1552430	Clock	clock circadian regulator	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:17445238
1552430	Clock	clock circadian regulator	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:9160756
1552430	Clock	clock circadian regulator	gene	MP:0020468	abnormal circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:23580255
1552430	Clock	clock circadian regulator	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:23580255
1552430	Clock	clock circadian regulator	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:8171325
1552430	Clock	clock circadian regulator	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:9160756
1552430	Clock	clock circadian regulator	gene	MP:0020471	abnormal circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:8171325
1552430	Clock	clock circadian regulator	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:8171325
1552430	Clock	clock circadian regulator	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:15967985
1552430	Clock	clock circadian regulator	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:16675400
1552430	Clock	clock circadian regulator	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:17445238
1552430	Clock	clock circadian regulator	gene	MP:0020474	advanced circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:16675400
1552430	Clock	clock circadian regulator	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20171012	MGI			PMID:15845877
1552430	Clock	clock circadian regulator	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20171012	MGI			PMID:11050136
1552430	Clock	clock circadian regulator	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20171012	MGI			PMID:11388430
1552430	Clock	clock circadian regulator	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20171012	MGI			PMID:16732766
1552430	Clock	clock circadian regulator	gene	MP:0030973	impaired gluconeogenesis		IAGP		N	RGD:5509061	20200102	MGI			PMID:15523558
1552432	Ppp4r3a	protein phosphatase 4 regulatory subunit 3A	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1552432	Ppp4r3a	protein phosphatase 4 regulatory subunit 3A	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1552432	Ppp4r3a	protein phosphatase 4 regulatory subunit 3A	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1552432	Ppp4r3a	protein phosphatase 4 regulatory subunit 3A	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1552432	Ppp4r3a	protein phosphatase 4 regulatory subunit 3A	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1552432	Ppp4r3a	protein phosphatase 4 regulatory subunit 3A	gene	MP:0020379	abnormal sucrose solution preference		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1552432	Ppp4r3a	protein phosphatase 4 regulatory subunit 3A	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20260402	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20250508	MGI			
1552434	Slco4c1	solute carrier organic anion transporter family, member 4C1	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20250508	MGI			
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0010040	abnormal oval cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552435	Entpd5	ectonucleoside triphosphate diphosphohydrolase 5	gene	MP:0010042	abnormal oval cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19176496
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0001790	abnormal immune system physiology		IEA		N	RGD:5509061	20111116	MGI			
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12847135
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16358363
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15897272
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15897272
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16358363
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15897272
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15897272
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182110
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15897272
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16358363
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606670
1552436	Pdcd1lg2	programmed cell death 1 ligand 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15897272
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20250508	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29237777
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:29237777
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20191107	MGI			PMID:29237777
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20191107	MGI			PMID:29237777
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20191107	MGI			PMID:29237777
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20191107	MGI			PMID:29237777
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230119	MGI			
1552437	Ccl28	C-C motif chemokine ligand 28	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20191107	MGI			PMID:29237777
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10716994
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10716994
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10716994
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20200310	MGI			
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20200310	MGI			
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10716994
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10716994
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0008213	absent immature B cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:9390689
1552438	Xrcc6	X-ray repair cross complementing 6	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294146
1552440	Spef1	sperm flagellar 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1552441	Selenbp1	selenium binding protein 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210520	MGI			
1552441	Selenbp1	selenium binding protein 1	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20210520	MGI			
1552441	Selenbp1	selenium binding protein 1	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23500078
1552441	Selenbp1	selenium binding protein 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220519	MGI			
1552441	Selenbp1	selenium binding protein 1	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23500078
1552441	Selenbp1	selenium binding protein 1	gene	MP:0002965	increased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23500078
1552441	Selenbp1	selenium binding protein 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1552441	Selenbp1	selenium binding protein 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23500078
1552441	Selenbp1	selenium binding protein 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23500078
1552441	Selenbp1	selenium binding protein 1	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23500078
1552441	Selenbp1	selenium binding protein 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1552441	Selenbp1	selenium binding protein 1	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1552441	Selenbp1	selenium binding protein 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180222	MGI			PMID:29255262
1552441	Selenbp1	selenium binding protein 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220519	MGI			
1552441	Selenbp1	selenium binding protein 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20180222	MGI			PMID:29255262
1552442	Bola1	bolA family member 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220519	MGI			
1552442	Bola1	bolA family member 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1552442	Bola1	bolA family member 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210826	MGI			
1552442	Bola1	bolA family member 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1552442	Bola1	bolA family member 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1552445	Polr3f	polymerase (RNA) III (DNA directed) polypeptide F	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20201022	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20200514	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20221215	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20200514	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20220519	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20221215	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210520	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201231	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20200514	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20200514	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1552449	Gnl1	guanine nucleotide binding protein-like 1	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20210520	MGI			
1552451	Scin	scinderin	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20160428	MGI			PMID:25681458
1552451	Scin	scinderin	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1552451	Scin	scinderin	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20160428	MGI			PMID:25681458
1552451	Scin	scinderin	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20160428	MGI			PMID:25681458
1552451	Scin	scinderin	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20160428	MGI			PMID:25681458
1552451	Scin	scinderin	gene	MP:0031722	abnormal podosome morphology		IAGP		N	RGD:5509061	20260507	MGI			PMID:25681458
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20181227	MGI			
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0003439	abnormal glycerol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0004156	abnormal QT variability		IEA		N	RGD:5509061	20260402	MGI			
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0011117	abnormal susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0013404	decreased circulating lactate level		IAGP		N	RGD:5509061	20141225	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:21803289
1552454	Slc13a5	solute carrier family 13 (sodium-dependent citrate transporter), member 5	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:21803289
1552455	Fas	Fas cell surface death receptor	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1416659
1552455	Fas	Fas cell surface death receptor	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2708160
1552455	Fas	Fas cell surface death receptor	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8793508
1552455	Fas	Fas cell surface death receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1552455	Fas	Fas cell surface death receptor	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1552455	Fas	Fas cell surface death receptor	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1552455	Fas	Fas cell surface death receptor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9036998
1552455	Fas	Fas cell surface death receptor	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1552455	Fas	Fas cell surface death receptor	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787314
1552455	Fas	Fas cell surface death receptor	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118350
1552455	Fas	Fas cell surface death receptor	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581453
1552455	Fas	Fas cell surface death receptor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10878371
1552455	Fas	Fas cell surface death receptor	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118350
1552455	Fas	Fas cell surface death receptor	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628400
1552455	Fas	Fas cell surface death receptor	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581453
1552455	Fas	Fas cell surface death receptor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11801636
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787314
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19528538
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581453
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671629
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0000701	abnormal lymph node size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0000701	abnormal lymph node size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11035071
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787314
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:2302830
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:6975351
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540652
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581453
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:762500
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671629
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787314
1552455	Fas	Fas cell surface death receptor	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736651
1552455	Fas	Fas cell surface death receptor	gene	MP:0001017	abnormal stellate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:9036998
1552455	Fas	Fas cell surface death receptor	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1552455	Fas	Fas cell surface death receptor	gene	MP:0001220	epidermal necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787314
1552455	Fas	Fas cell surface death receptor	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1552455	Fas	Fas cell surface death receptor	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1552455	Fas	Fas cell surface death receptor	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1552455	Fas	Fas cell surface death receptor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787314
1552455	Fas	Fas cell surface death receptor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8496852
1552455	Fas	Fas cell surface death receptor	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8496852
1552455	Fas	Fas cell surface death receptor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15192051
1552455	Fas	Fas cell surface death receptor	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118350
1552455	Fas	Fas cell surface death receptor	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1552455	Fas	Fas cell surface death receptor	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:9036998
1552455	Fas	Fas cell surface death receptor	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11801636
1552455	Fas	Fas cell surface death receptor	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11035071
1552455	Fas	Fas cell surface death receptor	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11035071
1552455	Fas	Fas cell surface death receptor	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9036998
1552455	Fas	Fas cell surface death receptor	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
1552455	Fas	Fas cell surface death receptor	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11035071
1552455	Fas	Fas cell surface death receptor	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
1552455	Fas	Fas cell surface death receptor	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:15192051
1552455	Fas	Fas cell surface death receptor	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0001830	decreased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:2302830
1552455	Fas	Fas cell surface death receptor	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:2708160
1552455	Fas	Fas cell surface death receptor	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736651
1552455	Fas	Fas cell surface death receptor	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17208228
1552455	Fas	Fas cell surface death receptor	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9472669
1552455	Fas	Fas cell surface death receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11714837
1552455	Fas	Fas cell surface death receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15289505
1552455	Fas	Fas cell surface death receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0001863	blood vessel inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1565490
1552455	Fas	Fas cell surface death receptor	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8163351
1552455	Fas	Fas cell surface death receptor	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787314
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:6975351
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540652
1552455	Fas	Fas cell surface death receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581453
1552455	Fas	Fas cell surface death receptor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11801636
1552455	Fas	Fas cell surface death receptor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1552455	Fas	Fas cell surface death receptor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9036998
1552455	Fas	Fas cell surface death receptor	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9472669
1552455	Fas	Fas cell surface death receptor	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0002148	abnormal hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:2302830
1552455	Fas	Fas cell surface death receptor	gene	MP:0002148	abnormal hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0002148	abnormal hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581453
1552455	Fas	Fas cell surface death receptor	gene	MP:0002148	abnormal hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0002163	abnormal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8163351
1552455	Fas	Fas cell surface death receptor	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20150108	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581453
1552455	Fas	Fas cell surface death receptor	gene	MP:0002224	abnormal spleen size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0002334	abnormal airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11590380
1552455	Fas	Fas cell surface death receptor	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0002375	abnormal thymus medulla morphology		IEA		N	RGD:5509061	20111116	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15980239
1552455	Fas	Fas cell surface death receptor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
1552455	Fas	Fas cell surface death receptor	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677469
1552455	Fas	Fas cell surface death receptor	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3009614
1552455	Fas	Fas cell surface death receptor	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9036998
1552455	Fas	Fas cell surface death receptor	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325838
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6444324
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8671629
1552455	Fas	Fas cell surface death receptor	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11035071
1552455	Fas	Fas cell surface death receptor	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
1552455	Fas	Fas cell surface death receptor	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2302830
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2302830
1552455	Fas	Fas cell surface death receptor	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0002533	abnormal type III hypersensitivity reaction		IEA		N	RGD:5509061	20111116	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18055812
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9472669
1552455	Fas	Fas cell surface death receptor	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0002936	joint swelling		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11035071
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9472669
1552455	Fas	Fas cell surface death receptor	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1552455	Fas	Fas cell surface death receptor	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20111116	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11567045
1552455	Fas	Fas cell surface death receptor	gene	MP:0003504	thyroid gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628400
1552455	Fas	Fas cell surface death receptor	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971023
1552455	Fas	Fas cell surface death receptor	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11035071
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325838
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2302830
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8496852
1552455	Fas	Fas cell surface death receptor	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10607487
1552455	Fas	Fas cell surface death receptor	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9036998
1552455	Fas	Fas cell surface death receptor	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1552455	Fas	Fas cell surface death receptor	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8163351
1552455	Fas	Fas cell surface death receptor	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0003946	renal necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10946317
1552455	Fas	Fas cell surface death receptor	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0004367	abnormal strial intermediate cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1416659
1552455	Fas	Fas cell surface death receptor	gene	MP:0004368	abnormal stria vascularis vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8793508
1552455	Fas	Fas cell surface death receptor	gene	MP:0004481	abnormal conjunctival epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17208228
1552455	Fas	Fas cell surface death receptor	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628400
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11801636
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486097
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325838
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6444324
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9036998
1552455	Fas	Fas cell surface death receptor	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11067882
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11801636
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325838
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2406366
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6975351
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8496852
1552455	Fas	Fas cell surface death receptor	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8793508
1552455	Fas	Fas cell surface death receptor	gene	MP:0004795	decreased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0004795	decreased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0004795	decreased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0004798	decreased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0004798	decreased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0004798	decreased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0004798	decreased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16237080
1552455	Fas	Fas cell surface death receptor	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325838
1552455	Fas	Fas cell surface death receptor	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8793508
1552455	Fas	Fas cell surface death receptor	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20210506	MGI			PMID:32547538
1552455	Fas	Fas cell surface death receptor	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10946317
1552455	Fas	Fas cell surface death receptor	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:14530378
1552455	Fas	Fas cell surface death receptor	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10946317
1552455	Fas	Fas cell surface death receptor	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12525697
1552455	Fas	Fas cell surface death receptor	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9094710
1552455	Fas	Fas cell surface death receptor	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:762500
1552455	Fas	Fas cell surface death receptor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:2302830
1552455	Fas	Fas cell surface death receptor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8793508
1552455	Fas	Fas cell surface death receptor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0004955	increased thymus weight		IEA		N	RGD:5509061	20111116	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0005002	abnormal T cell clonal deletion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11590380
1552455	Fas	Fas cell surface death receptor	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581453
1552455	Fas	Fas cell surface death receptor	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11035071
1552455	Fas	Fas cell surface death receptor	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540652
1552455	Fas	Fas cell surface death receptor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9075933
1552455	Fas	Fas cell surface death receptor	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594834
1552455	Fas	Fas cell surface death receptor	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6610701
1552455	Fas	Fas cell surface death receptor	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540652
1552455	Fas	Fas cell surface death receptor	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:3009614
1552455	Fas	Fas cell surface death receptor	gene	MP:0005141	liver hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7581453
1552455	Fas	Fas cell surface death receptor	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325838
1552455	Fas	Fas cell surface death receptor	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0005265	abnormal blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11801636
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9472669
1552455	Fas	Fas cell surface death receptor	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8496852
1552455	Fas	Fas cell surface death receptor	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18325838
1552455	Fas	Fas cell surface death receptor	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:762500
1552455	Fas	Fas cell surface death receptor	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:11801636
1552455	Fas	Fas cell surface death receptor	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6444324
1552455	Fas	Fas cell surface death receptor	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1552455	Fas	Fas cell surface death receptor	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9472669
1552455	Fas	Fas cell surface death receptor	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0005566	decreased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20111116	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12974753
1552455	Fas	Fas cell surface death receptor	gene	MP:0005614	decreased susceptibility to type III hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0005615	increased susceptibility to type III hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8793508
1552455	Fas	Fas cell surface death receptor	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11590380
1552455	Fas	Fas cell surface death receptor	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16527894
1552455	Fas	Fas cell surface death receptor	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10453074
1552455	Fas	Fas cell surface death receptor	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8496852
1552455	Fas	Fas cell surface death receptor	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736651
1552455	Fas	Fas cell surface death receptor	gene	MP:0006099	thin cerebellar granule layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787313
1552455	Fas	Fas cell surface death receptor	gene	MP:0006315	abnormal urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3009614
1552455	Fas	Fas cell surface death receptor	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:762500
1552455	Fas	Fas cell surface death receptor	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20150108	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21479271
1552455	Fas	Fas cell surface death receptor	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1552455	Fas	Fas cell surface death receptor	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339515
1552455	Fas	Fas cell surface death receptor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17509906
1552455	Fas	Fas cell surface death receptor	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008136	enlarged Peyer's patches		IEA		N	RGD:5509061	20111116	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008180	abnormal marginal zone B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486097
1552455	Fas	Fas cell surface death receptor	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0008206	increased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11035071
1552455	Fas	Fas cell surface death receptor	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11971023
1552455	Fas	Fas cell surface death receptor	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540652
1552455	Fas	Fas cell surface death receptor	gene	MP:0008350	increased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7540652
1552455	Fas	Fas cell surface death receptor	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18492657
1552455	Fas	Fas cell surface death receptor	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9109438
1552455	Fas	Fas cell surface death receptor	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23997217
1552455	Fas	Fas cell surface death receptor	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11737079
1552455	Fas	Fas cell surface death receptor	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15265950
1552455	Fas	Fas cell surface death receptor	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1552455	Fas	Fas cell surface death receptor	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8700897
1552455	Fas	Fas cell surface death receptor	gene	MP:0008542	enlarged cervical lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11801636
1552455	Fas	Fas cell surface death receptor	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0008573	increased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301622
1552455	Fas	Fas cell surface death receptor	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:6610701
1552455	Fas	Fas cell surface death receptor	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:6975351
1552455	Fas	Fas cell surface death receptor	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1552455	Fas	Fas cell surface death receptor	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3009614
1552455	Fas	Fas cell surface death receptor	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0008766	abnormal B cell receptor editing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486097
1552455	Fas	Fas cell surface death receptor	gene	MP:0008769	abnormal plasmacytoid dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1552455	Fas	Fas cell surface death receptor	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118350
1552455	Fas	Fas cell surface death receptor	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:6444324
1552455	Fas	Fas cell surface death receptor	gene	MP:0008879	submandibular gland inflammation		IAGP		N	RGD:5509061	20141218	MGI			PMID:7957574
1552455	Fas	Fas cell surface death receptor	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1565490
1552455	Fas	Fas cell surface death receptor	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17898284
1552455	Fas	Fas cell surface death receptor	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18055812
1552455	Fas	Fas cell surface death receptor	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141204	MGI			PMID:8163351
1552455	Fas	Fas cell surface death receptor	gene	MP:0008891	decreased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16118350
1552455	Fas	Fas cell surface death receptor	gene	MP:0008978	abnormal vagina weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10453074
1552455	Fas	Fas cell surface death receptor	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
1552455	Fas	Fas cell surface death receptor	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
1552455	Fas	Fas cell surface death receptor	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
1552455	Fas	Fas cell surface death receptor	gene	MP:0010065	decreased circulating creatine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0010138	arteritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9834083
1552455	Fas	Fas cell surface death receptor	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190328	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190328	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0010922	alveolitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148335
1552455	Fas	Fas cell surface death receptor	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0011081	decreased macrophage apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741297
1552455	Fas	Fas cell surface death receptor	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:16267157
1552455	Fas	Fas cell surface death receptor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0011369	increased renal glomerulus apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0011402	renal cast		IEA		N	RGD:5509061	20111116	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12097414
1552455	Fas	Fas cell surface death receptor	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18275831
1552455	Fas	Fas cell surface death receptor	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0011445	abnormal renal protein reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18779924
1552455	Fas	Fas cell surface death receptor	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0011483	renal glomerular synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:12571859
1552455	Fas	Fas cell surface death receptor	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1552455	Fas	Fas cell surface death receptor	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142777
1552455	Fas	Fas cell surface death receptor	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0011567	increased renal glomerulus lobularity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0011742	decreased urine nitrite level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9236188
1552455	Fas	Fas cell surface death receptor	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:1416659
1552455	Fas	Fas cell surface death receptor	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:2708160
1552455	Fas	Fas cell surface death receptor	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8793508
1552455	Fas	Fas cell surface death receptor	gene	MP:0012433	decreased ovarian tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505730
1552455	Fas	Fas cell surface death receptor	gene	MP:0013452	increased lacrimal gland apoptosis		IAGP		N	RGD:5509061	20150205	MGI			PMID:17898284
1552455	Fas	Fas cell surface death receptor	gene	MP:0013455	lacrimal gland atrophy		IAGP		N	RGD:5509061	20160324	MGI			PMID:1565490
1552455	Fas	Fas cell surface death receptor	gene	MP:0013585	thymus cortex atrophy		IEA		N	RGD:5509061	20150319	MGI			
1552455	Fas	Fas cell surface death receptor	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:16527894
1552455	Fas	Fas cell surface death receptor	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:11971023
1552455	Fas	Fas cell surface death receptor	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:17608689
1552455	Fas	Fas cell surface death receptor	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0020518	renal glomerular protein deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:16541466
1552455	Fas	Fas cell surface death receptor	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:16818796
1552455	Fas	Fas cell surface death receptor	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:17574818
1552455	Fas	Fas cell surface death receptor	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:23616572
1552455	Fas	Fas cell surface death receptor	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:9736651
1552455	Fas	Fas cell surface death receptor	gene	MP:0021186	decreased bone mineral density of vertebrae		IAGP		N	RGD:5509061	20220915	MGI			PMID:17259598
1552455	Fas	Fas cell surface death receptor	gene	MP:0031051	lymph node hemorrhage		IAGP		N	RGD:5509061	20200618	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0031051	lymph node hemorrhage		IAGP		N	RGD:5509061	20200618	MGI			PMID:6609979
1552455	Fas	Fas cell surface death receptor	gene	MP:0031052	lymph node necrosis		IAGP		N	RGD:5509061	20200618	MGI			PMID:309911
1552455	Fas	Fas cell surface death receptor	gene	MP:0031052	lymph node necrosis		IAGP		N	RGD:5509061	20200618	MGI			PMID:6609979
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18288109
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0002993	autoimmune arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17382885
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23805138
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17382885
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17382885
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008206	increased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16055554
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676052
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20151112	MGI			PMID:19706873
1552456	Bak1	BCL2-antagonist/killer 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11163212
1552458	Rnf146	ring finger protein 146	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0004189	abnormal alveolar process morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0011504	abnormal limb long bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20200310	MGI			PMID:28287403
1552458	Rnf146	ring finger protein 146	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0030009	increased bone marrow adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0030387	large posterior fontanelle		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0030439	decreased osteoblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0030471	abnormal ameloblast differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552458	Rnf146	ring finger protein 146	gene	MP:0030985	decreased circulating osteocalcin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28581440
1552461	Sdad1	SDA1 domain containing 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1552461	Sdad1	SDA1 domain containing 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20210930	MGI			PMID:33905568
1552462	Fuca2	fucosidase, alpha-L- 2, plasma	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170406	MGI			
1552463	Pex5l	peroxisomal biogenesis factor 5-like	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593326
1552463	Pex5l	peroxisomal biogenesis factor 5-like	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593326
1552463	Pex5l	peroxisomal biogenesis factor 5-like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555075
1552463	Pex5l	peroxisomal biogenesis factor 5-like	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593326
1552463	Pex5l	peroxisomal biogenesis factor 5-like	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593326
1552463	Pex5l	peroxisomal biogenesis factor 5-like	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593326
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000263	absent organized vascular network		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000264	failure of vascular branching		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000264	failure of vascular branching		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20200514	MGI			
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000293	absent myocardial trabeculae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0000296	absent trabeculae carneae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7477259
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:25202984
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20150212	MGI			PMID:25202984
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15899871
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596437
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20150528	MGI			PMID:25686605
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10498691
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9683559
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0031213	increased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:25202984
1552464	Tek	TEK receptor tyrosine kinase	gene	MP:0031500	increased cornea size		IAGP		N	RGD:5509061	20230810	MGI			PMID:25202984
1552466	Nit1	nitrilase 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16864578
1552466	Nit1	nitrilase 1	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:16864578
1552466	Nit1	nitrilase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16864578
1552466	Nit1	nitrilase 1	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16864578
1552466	Nit1	nitrilase 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16864578
1552468	Dld	dihydrolipoamide dehydrogenase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405644
1552468	Dld	dihydrolipoamide dehydrogenase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405644
1552468	Dld	dihydrolipoamide dehydrogenase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405644
1552468	Dld	dihydrolipoamide dehydrogenase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405644
1552468	Dld	dihydrolipoamide dehydrogenase	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9405644
1552470	Kifc1	kinesin family member C1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1552470	Kifc1	kinesin family member C1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1552471	Abhd10	abhydrolase domain containing 10	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1552471	Abhd10	abhydrolase domain containing 10	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1552471	Abhd10	abhydrolase domain containing 10	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993262
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993262
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0014390	decreased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:16327803
1552474	Dnaja3	DnaJ heat shock protein family (Hsp40) member A3	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20250911	MGI			PMID:16327803
1552475	Serpinb6a	serine (or cysteine) peptidase inhibitor, clade B, member 6a	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15082799
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210520	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230601	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210520	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1552478	Rrbp1	ribosome binding protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1552483	Tm2d2	TM2 domain containing 2	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20201022	MGI			
1552483	Tm2d2	TM2 domain containing 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20221215	MGI			
1552483	Tm2d2	TM2 domain containing 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1552483	Tm2d2	TM2 domain containing 2	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1552483	Tm2d2	TM2 domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552484	Bbc3	BCL2 binding component 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287039
1552484	Bbc3	BCL2 binding component 3	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585359
1552484	Bbc3	BCL2 binding component 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20818388
1552484	Bbc3	BCL2 binding component 3	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077368
1552484	Bbc3	BCL2 binding component 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077368
1552484	Bbc3	BCL2 binding component 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077368
1552484	Bbc3	BCL2 binding component 3	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077368
1552484	Bbc3	BCL2 binding component 3	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18048346
1552484	Bbc3	BCL2 binding component 3	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16399862
1552484	Bbc3	BCL2 binding component 3	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500851
1552484	Bbc3	BCL2 binding component 3	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585359
1552484	Bbc3	BCL2 binding component 3	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585359
1552484	Bbc3	BCL2 binding component 3	gene	MP:0003823	increased left ventricle developed pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16399862
1552484	Bbc3	BCL2 binding component 3	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287039
1552484	Bbc3	BCL2 binding component 3	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032672
1552484	Bbc3	BCL2 binding component 3	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077368
1552484	Bbc3	BCL2 binding component 3	gene	MP:0005571	decreased lactate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16399862
1552484	Bbc3	BCL2 binding component 3	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16399862
1552484	Bbc3	BCL2 binding component 3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287039
1552484	Bbc3	BCL2 binding component 3	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18287039
1552484	Bbc3	BCL2 binding component 3	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14500851
1552484	Bbc3	BCL2 binding component 3	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18077368
1552484	Bbc3	BCL2 binding component 3	gene	MP:0010754	abnormal heart left ventricle pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16399862
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20251002	MGI			PMID:40836090
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210826	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20220519	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20251002	MGI			PMID:40836090
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220519	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20220519	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20230601	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20210826	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20230601	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20220519	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0001787	pericardial edema		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220811	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220519	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20220519	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20220519	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20230601	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20251002	MGI			PMID:40836090
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20251002	MGI			PMID:40836090
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20251002	MGI			PMID:40836090
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20251002	MGI			PMID:40836090
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0010031	abnormal cranium size		IAGP		N	RGD:5509061	20251002	MGI			PMID:40836090
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0012270	cardiac edema		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0014134	abnormal embryo morphology		IEA		N	RGD:5509061	20251211	MGI			
1552485	Tgds	TDP-glucose 4,6-dehydratase	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20201022	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20201022	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20201022	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20201022	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20201022	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552486	Pdhb	pyruvate dehydrogenase (lipoamide) beta	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552487	Zfp52	zinc finger protein 52	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20210128	MGI			
1552487	Zfp52	zinc finger protein 52	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1552487	Zfp52	zinc finger protein 52	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1552487	Zfp52	zinc finger protein 52	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1552488	Erlin2	ER lipid raft associated 2	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20210128	MGI			
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22045334
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:22045334
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:22552287
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:22045334
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22552287
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22552287
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:28107482
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22552287
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22045334
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0002174	abnormal gastrulation movements		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22552287
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22045334
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22552287
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0009309	increased small intestine adenocarcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22552287
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:22552287
1552490	Smurf2	SMAD specific E3 ubiquitin protein ligase 2	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811868
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:15593118
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811868
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0005398	decreased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15593118
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15593118
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811868
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811868
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811868
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811868
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811868
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0010935	increased airway resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552492	Ccr4	C-C motif chemokine receptor 4	gene	MP:0010936	decreased airway resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12154006
1552495	Rffl	ring finger and FYVE like domain containing protein	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1552495	Rffl	ring finger and FYVE like domain containing protein	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20210128	MGI			
1552495	Rffl	ring finger and FYVE like domain containing protein	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1552495	Rffl	ring finger and FYVE like domain containing protein	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1552495	Rffl	ring finger and FYVE like domain containing protein	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1552495	Rffl	ring finger and FYVE like domain containing protein	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1552495	Rffl	ring finger and FYVE like domain containing protein	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1552495	Rffl	ring finger and FYVE like domain containing protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19138581
1552499	F12	coagulation factor XII (Hageman factor)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15351846
1552499	F12	coagulation factor XII (Hageman factor)	gene	MP:0003075	abnormal response to CNS ischemic injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533887
1552499	F12	coagulation factor XII (Hageman factor)	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16533887
1552499	F12	coagulation factor XII (Hageman factor)	gene	MP:0009812	abnormal bradykinin level		IAGP		N	RGD:5509061	20170323	MGI			PMID:16732380
1552499	F12	coagulation factor XII (Hageman factor)	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20170323	MGI			PMID:16732380
1552505	Sars1	seryl-tRNA synthetase 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20191128	MGI			
1552505	Sars1	seryl-tRNA synthetase 1	gene	MP:0005102	abnormal iris pigmentation		IEA		N	RGD:5509061	20231207	MGI			
1552505	Sars1	seryl-tRNA synthetase 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1552505	Sars1	seryl-tRNA synthetase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20231207	MGI			
1552505	Sars1	seryl-tRNA synthetase 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20191128	MGI			
1552505	Sars1	seryl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1552505	Sars1	seryl-tRNA synthetase 1	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20191128	MGI			
1552505	Sars1	seryl-tRNA synthetase 1	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20191128	MGI			
1552505	Sars1	seryl-tRNA synthetase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000105	impaired ossification of basisphenoid bone		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240627	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20210520	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20210826	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0002998	abnormal bone remodeling		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0003842	abnormal metopic suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004282	retrognathia		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004421	enlarged parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004454	absent pterygoid process		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0010043	abnormal frontonasal suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0011642	abnormal bone collagen fibril morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0012546	triangular face		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0014012	abnormal cranial blood vasculature morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0020301	short tongue		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20170921	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0030067	narrow face		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0030069	broad face		IAGP		N	RGD:5509061	20170921	MGI			PMID:17986521
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0030316	enlarged neurocranium		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0030533	abnormal snout skin morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:33996804
1552507	Ankrd11	ankyrin repeat domain 11	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:33996804
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20260402	MGI			
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0011015	decreased body surface temperature		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0020426	abnormal beige fat cell physiology		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0020520	whitened brown adipose tissue morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552508	Letmd1	LETM1 domain containing 1	gene	MP:0020522	decreased susceptibility to xenobiotic induced hyperthermia		IAGP		N	RGD:5509061	20220324	MGI			PMID:34910916
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22082675
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20220519	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505176
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210826	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505176
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20220519	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505176
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505176
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0003547	abnormal pulmonary pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22082675
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22082675
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20220519	MGI			
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22082675
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505176
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0005629	abnormal lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505176
1552509	Nol3	nucleolar protein 3 (apoptosis repressor with CARD domain)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22082675
1552510	Or51e1	olfactory receptor family 51 subfamily E member 1	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20240404	MGI			PMID:38507492
1552510	Or51e1	olfactory receptor family 51 subfamily E member 1	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20240404	MGI			PMID:38507492
1552510	Or51e1	olfactory receptor family 51 subfamily E member 1	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20240404	MGI			PMID:38507492
1552510	Or51e1	olfactory receptor family 51 subfamily E member 1	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20240404	MGI			PMID:38507492
1552510	Or51e1	olfactory receptor family 51 subfamily E member 1	gene	MP:0005583	decreased renin activity		IAGP		N	RGD:5509061	20240404	MGI			PMID:38507492
1552510	Or51e1	olfactory receptor family 51 subfamily E member 1	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20240404	MGI			PMID:38507492
1552510	Or51e1	olfactory receptor family 51 subfamily E member 1	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20240404	MGI			PMID:38507492
1552510	Or51e1	olfactory receptor family 51 subfamily E member 1	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20240404	MGI			PMID:38507492
1552510	Or51e1	olfactory receptor family 51 subfamily E member 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20240404	MGI			PMID:38507492
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003066	increased liver copper level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003067	decreased liver copper level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20190808	MGI			
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20190808	MGI			
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20190808	MGI			
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003952	abnormal copper level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0005636	abnormal mineral homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20190808	MGI			
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0009615	abnormal zinc homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0010157	abnormal small intestinal crypt cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0010248	decreased intestine copper level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22737083
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17483098
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552511	Slc39a4	solute carrier family 39 (zinc transporter), member 4	gene	MP:0020385	decreased intestine iron level		IAGP		N	RGD:5509061	20161020	MGI			PMID:22737083
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23720746
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23720746
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23720746
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23748901
1552512	Atat1	alpha tubulin acetyltransferase 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:23748901
1552513	Prickle2	prickle planar cell polarity protein 2	gene	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21276947
1552513	Prickle2	prickle planar cell polarity protein 2	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:21276947
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0004208	increased basal cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0014606	dark spleen		IAGP		N	RGD:5509061	20250206	MGI			PMID:18343975
1552516	Tom1l2	target of myb1-like 2 (chicken)	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:18343975
1552517	Eri1	exoribonuclease 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18438418
1552517	Eri1	exoribonuclease 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18438418
1552517	Eri1	exoribonuclease 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:18438418
1552517	Eri1	exoribonuclease 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18438418
1552517	Eri1	exoribonuclease 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18438418
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23896986
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23896986
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23896986
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0008823	abnormal interventricular septum membranous part morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23896986
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:28067313
1552518	Baiap2l1	BAI1-associated protein 2-like 1	gene	MP:0020102	increased hepatic glucose production		IAGP		N	RGD:5509061	20200310	MGI			PMID:23896986
1552524	Enpp5	ectonucleotide pyrophosphatase/phosphodiesterase 5	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1552524	Enpp5	ectonucleotide pyrophosphatase/phosphodiesterase 5	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20201022	MGI			
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0002082	postnatal lethality		IEA		N	RGD:5509061	20200310	MGI			
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210826	MGI			
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0008946	abnormal neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0009430	increased embryo weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210826	MGI			
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23643363
1552525	Smarcc2	SWI/SNF related BAF chromatin remodeling complex subunit C2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:26720614
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22375002
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:22375002
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20201015	MGI			PMID:26720614
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:22375002
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20201015	MGI			PMID:26720614
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201015	MGI			PMID:26720614
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:21273312
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:21273312
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20200310	MGI			PMID:21273312
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22375002
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22375002
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22375002
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22375002
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:22375002
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22833682
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22833682
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:21273312
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:26720614
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22375002
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21273312
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0014381	abnormal miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:21273312
1552526	Cc2d1a	coiled-coil and C2 domain containing 1A	gene	MP:0014384	increased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:21273312
1552527	Nceh1	neutral cholesterol ester hydrolase 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19723498
1552527	Nceh1	neutral cholesterol ester hydrolase 1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19723498
1552527	Nceh1	neutral cholesterol ester hydrolase 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19723498
1552527	Nceh1	neutral cholesterol ester hydrolase 1	gene	MP:0003193	decreased cholesterol efflux		IAGP		N	RGD:5509061	20200310	MGI			PMID:19723498
1552527	Nceh1	neutral cholesterol ester hydrolase 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19723498
1552527	Nceh1	neutral cholesterol ester hydrolase 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19723498
1552527	Nceh1	neutral cholesterol ester hydrolase 1	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19723498
1552527	Nceh1	neutral cholesterol ester hydrolase 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19723498
1552527	Nceh1	neutral cholesterol ester hydrolase 1	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20200310	MGI			PMID:15840715
1552533	Abhd14a	abhydrolase domain containing 14A	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1552533	Abhd14a	abhydrolase domain containing 14A	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1552535	Tpmt	thiopurine methyltransferase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510427
1552535	Tpmt	thiopurine methyltransferase	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510427
1552535	Tpmt	thiopurine methyltransferase	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510427
1552535	Tpmt	thiopurine methyltransferase	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510427
1552535	Tpmt	thiopurine methyltransferase	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17510427
1552537	Pkmyt1	protein kinase, membrane associated tyrosine/threonine 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20201022	MGI			
1552537	Pkmyt1	protein kinase, membrane associated tyrosine/threonine 1	gene	MP:0000603	pale liver		IEA		N	RGD:5509061	20210520	MGI			
1552537	Pkmyt1	protein kinase, membrane associated tyrosine/threonine 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20210520	MGI			
1552537	Pkmyt1	protein kinase, membrane associated tyrosine/threonine 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1552537	Pkmyt1	protein kinase, membrane associated tyrosine/threonine 1	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1552537	Pkmyt1	protein kinase, membrane associated tyrosine/threonine 1	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20210520	MGI			
1552537	Pkmyt1	protein kinase, membrane associated tyrosine/threonine 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1552537	Pkmyt1	protein kinase, membrane associated tyrosine/threonine 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552537	Pkmyt1	protein kinase, membrane associated tyrosine/threonine 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210826	MGI			
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20220331	MGI			PMID:34298397
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20200310	MGI			
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200310	MGI			
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:28874825
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:28874825
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200310	MGI			
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0013299	decreased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20220331	MGI			PMID:34298397
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0014046	abnormal mitophagy		IAGP		N	RGD:5509061	20220331	MGI			PMID:34221868
1552540	Atp5if1	ATP synthase inhibitory factor subunit 1	gene	MP:0014234	decreased enterocyte apoptosis		IAGP		N	RGD:5509061	20230323	MGI			PMID:34221868
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20160310	MGI			PMID:24905170
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592277
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592277
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592277
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0003279	aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0003394	increased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0004879	decreased systemic vascular resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:27027284
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592277
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592277
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592277
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19592277
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160310	MGI			PMID:24905170
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9859212
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141159
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0013026	decreased Ly6C low monocyte number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27814941
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367982
1552542	Klf2	Kruppel-like transcription factor 2 (lung)	gene	MP:0031589	detached epicardium		IAGP		N	RGD:5509061	20240229	MGI			PMID:17141159
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20220519	MGI			
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20211021	MGI			
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38011999
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:38011999
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0008526	decreased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0010031	abnormal cranium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22234171
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552543	Eif4h	eukaryotic translation initiation factor 4H	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23835334
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0001560	abnormal circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20023287
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0003221	abnormal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0003948	abnormal gas homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23835334
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005288	abnormal oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20023287
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:20023287
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0006087	increased body mass index		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20023287
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0008908	increased total fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009119	increased brown fat cell size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009294	increased interscapular fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009302	increased renal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20023287
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0012236	abnormal cholangiocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0012270	cardiac edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0014071	increased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:20023287
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20260219	MGI			PMID:36934843
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20200310	MGI			PMID:21641555
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21465509
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23835334
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0031418	increased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:16675698
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0031418	increased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:21857651
1552545	Pnpla2	patatin-like phospholipase domain containing 2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:16675698
1552548	Tm9sf2	transmembrane 9 superfamily member 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1552548	Tm9sf2	transmembrane 9 superfamily member 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220519	MGI			
1552548	Tm9sf2	transmembrane 9 superfamily member 2	gene	MP:0002161	abnormal fertility/fecundity		IEA		N	RGD:5509061	20251211	MGI			
1552548	Tm9sf2	transmembrane 9 superfamily member 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20220519	MGI			
1552548	Tm9sf2	transmembrane 9 superfamily member 2	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220519	MGI			
1552548	Tm9sf2	transmembrane 9 superfamily member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1552548	Tm9sf2	transmembrane 9 superfamily member 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1552550	Parp9	poly (ADP-ribose) polymerase family, member 9	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20210805	MGI			PMID:33976210
1552550	Parp9	poly (ADP-ribose) polymerase family, member 9	gene	MP:0031704	decreased interferon type I secretion		IAGP		N	RGD:5509061	20260402	MGI			PMID:33976210
1552550	Parp9	poly (ADP-ribose) polymerase family, member 9	gene	MP:0031707	decreased circulating interferon type I level		IAGP		N	RGD:5509061	20260402	MGI			PMID:33976210
1552552	Hdac7	histone deacetylase 7	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210826	MGI			
1552552	Hdac7	histone deacetylase 7	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1552552	Hdac7	histone deacetylase 7	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873063
1552552	Hdac7	histone deacetylase 7	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20240523	MGI			
1552554	Memo1	mediator of cell motility 1	gene	MP:0000039	abnormal otic capsule morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20160811	MGI			
1552554	Memo1	mediator of cell motility 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0000653	abnormal sex gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20201231	MGI			
1552554	Memo1	mediator of cell motility 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1552554	Memo1	mediator of cell motility 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1552554	Memo1	mediator of cell motility 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
1552554	Memo1	mediator of cell motility 1	gene	MP:0004450	presphenoid bone hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0004461	basisphenoid bone hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0008275	failure of endochondral bone ossification		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0009892	palate bone hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0009896	palatine bone horizontal plate hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0012337	increased vitamin D level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24056085
1552554	Memo1	mediator of cell motility 1	gene	MP:0013807	generalized edema		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0030027	basioccipital bone hypoplasia		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0030033	abnormal nasal bridge morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0030351	wide coronal suture		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552554	Memo1	mediator of cell motility 1	gene	MP:0030467	abnormal cranial cartilage development		IAGP		N	RGD:5509061	20230504	MGI			PMID:26746790
1552555	Lgmn	legumain	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1552555	Lgmn	legumain	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12775715
1552555	Lgmn	legumain	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879164
1552555	Lgmn	legumain	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1552555	Lgmn	legumain	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0005060	accumulation of giant lysosomes in kidney/renal tubule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12775715
1552555	Lgmn	legumain	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12775715
1552555	Lgmn	legumain	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879164
1552555	Lgmn	legumain	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879164
1552555	Lgmn	legumain	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19879164
1552555	Lgmn	legumain	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1552555	Lgmn	legumain	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19106291
1552555	Lgmn	legumain	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0011379	abnormal kidney outer medulla outer stripe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0011423	kidney cortex atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0011425	abnormal kidney interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21292981
1552555	Lgmn	legumain	gene	MP:0014606	dark spleen		IAGP		N	RGD:5509061	20250206	MGI			PMID:19106291
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645591
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17347480
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17251423
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19705551
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17251423
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:18341994
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001756	abnormal urination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12161756
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19794112
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:10764638
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128844
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263443
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19244541
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:19705551
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821274
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327782
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943565
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509739
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943565
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19794112
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002733	abnormal thermal nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821274
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553498
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10764638
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10821274
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19705551
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002917	decreased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:18341994
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19794112
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0003022	increased coronary flow rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314376
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10764638
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263443
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19705551
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0003821	decreased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314376
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0003823	increased left ventricle developed pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314376
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0003829	impaired febrile response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15763167
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314376
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19155296
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20151217	MGI			PMID:24462040
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20240530	MGI			PMID:33358893
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17251423
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15266010
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19794112
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19794112
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15509739
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18503767
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:10764638
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19794112
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19794112
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19794112
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:15763167
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18503767
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008859	abnormal hair cycle catagen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645591
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008860	abnormal hair cycle telogen phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:16645591
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15121805
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128844
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553498
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18341994
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0008997	increased blood osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16327782
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18503767
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0009287	decreased abdominal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18503767
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17251423
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17251423
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19794112
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0009755	impaired behavioral response to alcohol		IAGP		N	RGD:5509061	20141003	MGI			PMID:19705551
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0010055	abnormal sensory neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10764638
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0010055	abnormal sensory neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18499726
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0010072	increased pruritus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23263443
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0010073	decreased pruritus		IAGP		N	RGD:5509061	20240530	MGI			PMID:33358893
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943565
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20180125	MGI			PMID:18503767
1552559	Trpv1	transient receptor potential cation channel, subfamily V, member 1	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:18503767
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20111116	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20171109	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20141003	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20171109	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20141003	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0001156	abnormal spermatogenesis		IEA		N	RGD:5509061	20111116	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0001577	anemia		IEA		N	RGD:5509061	20111116	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20171109	MGI			PMID:6831040
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20627074
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002209	decreased germ cell number		IEA		N	RGD:5509061	20111116	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20141003	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20171109	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20171109	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0003950	abnormal plasma membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20627074
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20171109	MGI			PMID:6466874
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20627074
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:6466874
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0005114	premature hair loss		IEA		N	RGD:5509061	20111116	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0005431	decreased oocyte number		IEA		N	RGD:5509061	20111222	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20141003	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20627074
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20171109	MGI			PMID:16219534
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20627074
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0009859	eye opacity		IEA		N	RGD:5509061	20150326	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160804	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20460369
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0012010	parturition failure		IAGP		N	RGD:5509061	20191219	MGI			PMID:1756209
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0013539	increased ovary adenoma incidence		IEA		N	RGD:5509061	20150326	MGI			
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0014693	abnormal cell nucleus size		IAGP		N	RGD:5509061	20250710	MGI			PMID:20627074
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:4596202
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20240718	MGI			PMID:34237032
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:20627074
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0030944	abnormal pericentriolar material morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:20627074
1552560	Cdk5rap2	CDK5 regulatory subunit associated protein 2	gene	MP:0031682	abnormal centriole morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:20627074
1552564	Lyl1	lymphoblastomic leukemia 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514064
1552564	Lyl1	lymphoblastomic leukemia 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514064
1552564	Lyl1	lymphoblastomic leukemia 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387538
1552564	Lyl1	lymphoblastomic leukemia 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514064
1552564	Lyl1	lymphoblastomic leukemia 1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16514064
1552564	Lyl1	lymphoblastomic leukemia 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21387538
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0000534	abnormal ureter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0002990	short ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0003827	abnormal Wolffian duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0003942	abnormal urinary system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0004967	abnormal kidney epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0009085	abnormal uterine horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0010980	ectopic ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0011803	double kidney pelvis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949185
1552566	Lzts2	leucine zipper, putative tumor suppressor 2	gene	MP:0013320	dilated seminal vesicle		IAGP		N	RGD:5509061	20141204	MGI			PMID:21949185
1552569	Veph1	ventricular zone expressed PH domain-containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15388229
1552570	Lcn9	lipocalin 9	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20241128	MGI			PMID:36428102
1552570	Lcn9	lipocalin 9	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20241128	MGI			PMID:36428102
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12405636
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8510385
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8510385
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8510385
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12405636
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8510385
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17928412
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:8510385
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20141003	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:12405636
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0004875	increased mean systemic arterial blood pressure		IEA		N	RGD:5509061	20190103	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8510385
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IEA		N	RGD:5509061	20190103	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0006144	increased systemic arterial systolic blood pressure		IEA		N	RGD:5509061	20190103	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12405636
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0008537	increased susceptibility to induced colitis		IEA		N	RGD:5509061	20190103	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0010422	heart right ventricle hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0010845	decreased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20190103	MGI			
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0011249	abdominal situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12405636
1552572	Nek8	NIMA (never in mitosis gene a)-related expressed kinase 8	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:23274954
1552573	Pax3	paired box 3	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1552573	Pax3	paired box 3	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1552573	Pax3	paired box 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1552573	Pax3	paired box 3	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
1552573	Pax3	paired box 3	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0000371	diluted coat color		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857794
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:14170406
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951257
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095975
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20160616	MGI			PMID:26952979
1552573	Pax3	paired box 3	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1552573	Pax3	paired box 3	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1552573	Pax3	paired box 3	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1552573	Pax3	paired box 3	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0000585	kinked tail		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951257
1552573	Pax3	paired box 3	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1552573	Pax3	paired box 3	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600971
1552573	Pax3	paired box 3	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631247
1552573	Pax3	paired box 3	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785297
1552573	Pax3	paired box 3	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1552573	Pax3	paired box 3	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843801
1552573	Pax3	paired box 3	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785297
1552573	Pax3	paired box 3	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20150528	MGI			PMID:7976186
1552573	Pax3	paired box 3	gene	MP:0000822	abnormal brain ventricle morphology		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7976186
1552573	Pax3	paired box 3	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1552573	Pax3	paired box 3	gene	MP:0000898	midbrain hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10699180
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095975
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:2763211
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7976186
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1552573	Pax3	paired box 3	gene	MP:0000919	cranioschisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:7976186
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10699180
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11914272
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12358782
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:4826095
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0000936	small embryonic telencephalon		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0000959	abnormal somatic sensory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
1552573	Pax3	paired box 3	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1552573	Pax3	paired box 3	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2763211
1552573	Pax3	paired box 3	gene	MP:0000962	disorganized dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:2763211
1552573	Pax3	paired box 3	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:26952979
1552573	Pax3	paired box 3	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0001063	abnormal trochlear nerve morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0001076	abnormal hypoglossal nerve morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1552573	Pax3	paired box 3	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0001189	absent skin pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330927
1552573	Pax3	paired box 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539826
1552573	Pax3	paired box 3	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1552573	Pax3	paired box 3	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1552573	Pax3	paired box 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330927
1552573	Pax3	paired box 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720875
1552573	Pax3	paired box 3	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8661050
1552573	Pax3	paired box 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1552573	Pax3	paired box 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1552573	Pax3	paired box 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1552573	Pax3	paired box 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539826
1552573	Pax3	paired box 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:23622066
1552573	Pax3	paired box 3	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489287
1552573	Pax3	paired box 3	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1552573	Pax3	paired box 3	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20160616	MGI			PMID:26952979
1552573	Pax3	paired box 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330927
1552573	Pax3	paired box 3	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10699180
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15729346
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095975
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650549
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2763211
1552573	Pax3	paired box 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:473084
1552573	Pax3	paired box 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857794
1552573	Pax3	paired box 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489287
1552573	Pax3	paired box 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650549
1552573	Pax3	paired box 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1552573	Pax3	paired box 3	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20160623	MGI			PMID:25807280
1552573	Pax3	paired box 3	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1552573	Pax3	paired box 3	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1552573	Pax3	paired box 3	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1552573	Pax3	paired box 3	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1552573	Pax3	paired box 3	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:23622066
1552573	Pax3	paired box 3	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1552573	Pax3	paired box 3	gene	MP:0002872	polycythemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1552573	Pax3	paired box 3	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095975
1552573	Pax3	paired box 3	gene	MP:0002938	white spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0002939	head spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857794
1552573	Pax3	paired box 3	gene	MP:0002939	head spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:14170406
1552573	Pax3	paired box 3	gene	MP:0002940	variable body spotting		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1552573	Pax3	paired box 3	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1552573	Pax3	paired box 3	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20150326	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:2763211
1552573	Pax3	paired box 3	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:10699180
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:16712836
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951257
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095975
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:2763211
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:6665745
1552573	Pax3	paired box 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631247
1552573	Pax3	paired box 3	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1552573	Pax3	paired box 3	gene	MP:0003246	loss of GABAergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1552573	Pax3	paired box 3	gene	MP:0003247	abnormal glutaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1552573	Pax3	paired box 3	gene	MP:0003248	loss of glutamate neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1552573	Pax3	paired box 3	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1552573	Pax3	paired box 3	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20150528	MGI			PMID:7976186
1552573	Pax3	paired box 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0003760	decreased palatal length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0003792	abnormal major salivary gland morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1552573	Pax3	paired box 3	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:4826095
1552573	Pax3	paired box 3	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1552573	Pax3	paired box 3	gene	MP:0003939	abnormal myotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1552573	Pax3	paired box 3	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951257
1552573	Pax3	paired box 3	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0004206	abnormal dermomyotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631247
1552573	Pax3	paired box 3	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0004248	abnormal epaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1552573	Pax3	paired box 3	gene	MP:0004289	abnormal bony labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1552573	Pax3	paired box 3	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1552573	Pax3	paired box 3	gene	MP:0004383	absent interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0004419	absent parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0004419	absent parietal bone		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1552573	Pax3	paired box 3	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0004454	absent pterygoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0004458	absent alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0004460	alisphenoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0004477	turbinate hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0004612	fusion of vertebral bodies		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0004760	increased mitotic index		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0004846	absent skeletal muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0004869	frontal bone hypoplasia		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0004914	absent ultimobranchial body		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1552573	Pax3	paired box 3	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1552573	Pax3	paired box 3	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1552573	Pax3	paired box 3	gene	MP:0005171	absent coat pigmentation		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1552573	Pax3	paired box 3	gene	MP:0005314	absent thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330927
1552573	Pax3	paired box 3	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1552573	Pax3	paired box 3	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0006030	abnormal otic vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1552573	Pax3	paired box 3	gene	MP:0006062	abnormal vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1552573	Pax3	paired box 3	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1552573	Pax3	paired box 3	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
1552573	Pax3	paired box 3	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0006284	absent hypaxial muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0008065	short endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:5912439
1552573	Pax3	paired box 3	gene	MP:0008237	abnormal ventral coat pigmentation		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0008301	adrenal medulla hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
1552573	Pax3	paired box 3	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0008460	absent dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0008460	absent dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0008460	absent dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:23622066
1552573	Pax3	paired box 3	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20150528	MGI			PMID:7976186
1552573	Pax3	paired box 3	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23622066
1552573	Pax3	paired box 3	gene	MP:0009245	caudal rachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14170406
1552573	Pax3	paired box 3	gene	MP:0009247	meteorism		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141225	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0009407	increased skeletal muscle fiber density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20141225	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24121508
1552573	Pax3	paired box 3	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0009909	bifid tongue		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0009933	abnormal tail hair pigmentation		IAGP		N	RGD:5509061	20160616	MGI			PMID:26952979
1552573	Pax3	paired box 3	gene	MP:0009933	abnormal tail hair pigmentation		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0009934	abnormal hind foot hair pigmentation		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198335
1552573	Pax3	paired box 3	gene	MP:0010016	variable depigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0010056	ectopic skeletal muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785297
1552573	Pax3	paired box 3	gene	MP:0010073	decreased pruritus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23622066
1552573	Pax3	paired box 3	gene	MP:0010231	transverse fur striping		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0010457	pulmonary artery stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330927
1552573	Pax3	paired box 3	gene	MP:0010459	supravalvar pulmonary trunk stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330927
1552573	Pax3	paired box 3	gene	MP:0010463	aorta stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330927
1552573	Pax3	paired box 3	gene	MP:0010572	persistent right dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
1552573	Pax3	paired box 3	gene	MP:0010589	common truncal valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0010628	patent tricuspid valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0010649	dilated pulmonary trunk		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539826
1552573	Pax3	paired box 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18330927
1552573	Pax3	paired box 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16906226
1552573	Pax3	paired box 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360543
1552573	Pax3	paired box 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1552573	Pax3	paired box 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14170406
1552573	Pax3	paired box 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16951257
1552573	Pax3	paired box 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21354128
1552573	Pax3	paired box 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539826
1552573	Pax3	paired box 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843801
1552573	Pax3	paired box 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20045680
1552573	Pax3	paired box 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095975
1552573	Pax3	paired box 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160512	MGI			PMID:14170406
1552573	Pax3	paired box 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410975
1552573	Pax3	paired box 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8661050
1552573	Pax3	paired box 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857794
1552573	Pax3	paired box 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1552573	Pax3	paired box 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21512107
1552573	Pax3	paired box 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0011102	embryonic lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1552573	Pax3	paired box 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20095975
1552573	Pax3	paired box 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9344762
1552573	Pax3	paired box 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1552573	Pax3	paired box 3	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1552573	Pax3	paired box 3	gene	MP:0011277	decreased tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21867959
1552573	Pax3	paired box 3	gene	MP:0012169	optic placode degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0012185	abnormal muscle precursor cell morphology		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
1552573	Pax3	paired box 3	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242297
1552573	Pax3	paired box 3	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15132998
1552573	Pax3	paired box 3	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483623
1552573	Pax3	paired box 3	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20231109	MGI			PMID:36400788
1552573	Pax3	paired box 3	gene	MP:0012547	spina bifida cystica		IEA		N	RGD:5509061	20141003	MGI			
1552573	Pax3	paired box 3	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11914272
1552573	Pax3	paired box 3	gene	MP:0012728	abnormal somite border morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14665670
1552573	Pax3	paired box 3	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2619088
1552573	Pax3	paired box 3	gene	MP:0012745	abnormal neural crest cell physiology		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
1552573	Pax3	paired box 3	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20231102	MGI			PMID:35899771
1552573	Pax3	paired box 3	gene	MP:0013264	tongue ankylosis		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0013720	abnormal mammary line morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:16720875
1552573	Pax3	paired box 3	gene	MP:0013721	abnormal mammary placode morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:16720875
1552573	Pax3	paired box 3	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:28043919
1552573	Pax3	paired box 3	gene	MP:0014167	ectopic bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20221013	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0021095	abnormal dorsal interneuron 4 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:18198335
1552573	Pax3	paired box 3	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:31241461
1552573	Pax3	paired box 3	gene	MP:0021216	abnormal palatal mesenchymal cell differentiation		IAGP		N	RGD:5509061	20230302	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0021217	abnormal palatal shelf bone ossification		IAGP		N	RGD:5509061	20230302	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0030031	abnormal forehead morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1552573	Pax3	paired box 3	gene	MP:0030056	lacrimal bone hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:15520281
1552573	Pax3	paired box 3	gene	MP:0030190	small snout		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1552573	Pax3	paired box 3	gene	MP:0030291	short soft palate		IAGP		N	RGD:5509061	20221020	MGI			PMID:17927973
1552573	Pax3	paired box 3	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20230309	MGI			PMID:23872235
1552573	Pax3	paired box 3	gene	MP:0030535	abnormal hypoglossal cord morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:16951257
1552573	Pax3	paired box 3	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:32692983
1552573	Pax3	paired box 3	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:9344762
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213450
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213450
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269668
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269668
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269668
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213450
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213450
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213450
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0003370	increased circulating estrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269668
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269668
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0004906	enlarged uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269668
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230119	MGI			
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0009092	endometrium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269668
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20241121	MGI			
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230119	MGI			
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20230119	MGI			
1552574	Chst10	carbohydrate sulfotransferase 10	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20260402	MGI			
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552575	Plpp7	phospholipid phosphatase 7 (inactive)	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20210311	MGI			PMID:33514739
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20250508	MGI			
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552576	Tmem106a	transmembrane protein 106A	gene	MP:0020344	abnormal susceptibility to injury induced morbidity/mortality		IAGP		N	RGD:5509061	20250130	MGI			PMID:33006758
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486155
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688600
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11961069
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0000740	impaired smooth muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486155
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0000742	impaired contractility of ileal smooth muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486155
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990086
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382674
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0001629	abnormal heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688600
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486155
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990086
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:15919709
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0002546	mydriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12486155
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18382674
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:16110248
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0005085	abnormal gallbladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11961069
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990086
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688600
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9990086
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0012125	decreased bronchoconstrictive response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645675
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:16110248
1552578	Chrm2	cholinergic receptor, muscarinic 2, cardiac	gene	MP:0031650	decreased mounting behavior		IAGP		N	RGD:5509061	20240905	MGI			PMID:18382674
1552581	Fgfbp1	fibroblast growth factor binding protein 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:28053031
1552581	Fgfbp1	fibroblast growth factor binding protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170706	MGI			PMID:28053031
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664684
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000084	abnormal fontanelle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664684
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664684
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215352
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741143
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741143
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741143
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19741143
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21752929
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15562281
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001296	macrophthalmia		IAGP		N	RGD:5509061	20141218	MGI			PMID:11929848
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660670
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141218	MGI			PMID:11929848
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001316	cornea scarring		IAGP		N	RGD:5509061	20141218	MGI			PMID:11929848
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001316	cornea scarring		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660670
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20141218	MGI			PMID:11929848
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:11929848
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18695238
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001375	abnormal mating preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441904
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18695238
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:18695238
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:11929848
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15007643
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19298015
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18695238
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:9664684
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15562281
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002892	decreased superior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215352
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956245
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215352
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660670
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21752929
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003687	abnormal intraocular muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003877	abnormal serotonergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17151281
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:18695238
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004096	abnormal midbrain-hindbrain boundary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004224	absent trabecular meshwork		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004284	abnormal Descemet membrane morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004360	absent ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004443	absent supraoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664684
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004508	abnormal pectoral girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004688	absent ilium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004694	absent patella		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215352
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004694	absent patella		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004861	abnormal Raphe nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17151281
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004861	abnormal Raphe nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18695238
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21752929
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005099	abnormal ciliary body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660670
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660670
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005208	abnormal iris stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660670
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10660670
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:11929848
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20160310	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956245
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956244
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956245
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215352
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20215352
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0006105	small tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0006230	iris stroma hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19298015
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956244
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956244
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956245
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008138	absent podocyte foot process		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956245
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:18695238
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008494	absence of all nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21752929
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21752929
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0009637	abnormal pretectal region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0009641	kidney degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0009825	cornea ulcer		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21246047
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956245
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956245
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9590288
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21752929
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956245
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011455	absent glomerular endothelium fenestra		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956245
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141218	MGI			PMID:11929848
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0011483	renal glomerular synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0012000	abnormal limb position		IAGP		N	RGD:5509061	20141218	MGI			PMID:24809698
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0012785	decreased rhombomere 1 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166916
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0013742	absent ciliary body		IAGP		N	RGD:5509061	20150416	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0013743	ciliary body hypoplasia		IAGP		N	RGD:5509061	20150416	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0014365	impaired short-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:25915474
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:21441904
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:10660670
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20201231	MGI			PMID:20568247
1552590	Lmx1b	LIM homeobox transcription factor 1 beta	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25915474
1552591	Hsp90ab1	heat shock protein 90 alpha (cytosolic), class B member 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654595
1552591	Hsp90ab1	heat shock protein 90 alpha (cytosolic), class B member 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654595
1552591	Hsp90ab1	heat shock protein 90 alpha (cytosolic), class B member 1	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654595
1552591	Hsp90ab1	heat shock protein 90 alpha (cytosolic), class B member 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654595
1552591	Hsp90ab1	heat shock protein 90 alpha (cytosolic), class B member 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654595
1552591	Hsp90ab1	heat shock protein 90 alpha (cytosolic), class B member 1	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10654595
1552592	Usp37	ubiquitin specific peptidase 37	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1552592	Usp37	ubiquitin specific peptidase 37	gene	MP:0011092	embryonic lethality, complete penetrance		IEA		N	RGD:5509061	20200310	MGI			
1552592	Usp37	ubiquitin specific peptidase 37	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0000154	rib fusion		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20230601	MGI			
1552593	Marveld3	MARVEL (membrane-associating) domain containing 3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1552596	Depdc1a	DEP domain containing 1a	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1552596	Depdc1a	DEP domain containing 1a	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1552600	Plekhm2	pleckstrin homology and RUN domain containing M2	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20200310	MGI			
1552600	Plekhm2	pleckstrin homology and RUN domain containing M2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26268777
1552600	Plekhm2	pleckstrin homology and RUN domain containing M2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1552600	Plekhm2	pleckstrin homology and RUN domain containing M2	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:26268777
1552600	Plekhm2	pleckstrin homology and RUN domain containing M2	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20200310	MGI			
1552600	Plekhm2	pleckstrin homology and RUN domain containing M2	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26268777
1552600	Plekhm2	pleckstrin homology and RUN domain containing M2	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:26268777
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0013916	decreased intestine length		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0014078	small intestinal villus atrophy		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0014222	decreased colon goblet cell number		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552601	Spint2	serine protease inhibitor, Kunitz type 2	gene	MP:0031154	intestinal hemorrhage		IAGP		N	RGD:5509061	20201224	MGI			PMID:29617460
1552604	Amigo1	adhesion molecule with Ig like domain 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1552604	Amigo1	adhesion molecule with Ig like domain 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210826	MGI			
1552604	Amigo1	adhesion molecule with Ig like domain 1	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:35169021
1552604	Amigo1	adhesion molecule with Ig like domain 1	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20230413	MGI			PMID:35169021
1552608	Kif3a	kinesin family member 3A	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166921
1552608	Kif3a	kinesin family member 3A	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166921
1552608	Kif3a	kinesin family member 3A	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1552608	Kif3a	kinesin family member 3A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166921
1552608	Kif3a	kinesin family member 3A	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1552608	Kif3a	kinesin family member 3A	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1552608	Kif3a	kinesin family member 3A	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1552608	Kif3a	kinesin family member 3A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1552608	Kif3a	kinesin family member 3A	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21745638
1552608	Kif3a	kinesin family member 3A	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0002239	abnormal nasal septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579360
1552608	Kif3a	kinesin family member 3A	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20200130	MGI			PMID:10943838
1552608	Kif3a	kinesin family member 3A	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1552608	Kif3a	kinesin family member 3A	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209331
1552608	Kif3a	kinesin family member 3A	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0004623	thoracic vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166921
1552608	Kif3a	kinesin family member 3A	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0005249	abnormal palatine bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166921
1552608	Kif3a	kinesin family member 3A	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20171109	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166921
1552608	Kif3a	kinesin family member 3A	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17166921
1552608	Kif3a	kinesin family member 3A	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579360
1552608	Kif3a	kinesin family member 3A	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579360
1552608	Kif3a	kinesin family member 3A	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200130	MGI			PMID:10943838
1552608	Kif3a	kinesin family member 3A	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579360
1552608	Kif3a	kinesin family member 3A	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20200130	MGI			PMID:10943838
1552608	Kif3a	kinesin family member 3A	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200130	MGI			PMID:10943838
1552608	Kif3a	kinesin family member 3A	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0009328	delayed heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0009377	ectopic manchette		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579360
1552608	Kif3a	kinesin family member 3A	gene	MP:0010500	myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220415
1552608	Kif3a	kinesin family member 3A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1552608	Kif3a	kinesin family member 3A	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0012093	absent nodal flow		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0012509	neural tube degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10330409
1552608	Kif3a	kinesin family member 3A	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0012759	increased cranial neural crest cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20240613	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0020384	absent kidney epithelial cell primary cilium		IAGP		N	RGD:5509061	20161013	MGI			PMID:12672950
1552608	Kif3a	kinesin family member 3A	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20190704	MGI			PMID:17359961
1552608	Kif3a	kinesin family member 3A	gene	MP:0030251	broad frontonasal prominence		IAGP		N	RGD:5509061	20171019	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0030269	absent mandibular ramus		IAGP		N	RGD:5509061	20171026	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0030276	anterior cranium occultum		IAGP		N	RGD:5509061	20171102	MGI			PMID:20106874
1552608	Kif3a	kinesin family member 3A	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0031373	abnormal manchette perinuclear ring morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0031375	abnormal manchette disassembly		IAGP		N	RGD:5509061	20220407	MGI			PMID:23831641
1552608	Kif3a	kinesin family member 3A	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20220428	MGI			PMID:23831641
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0009453	enhanced contextual conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0009787	increased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20190110	MGI			PMID:30442668
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20190110	MGI			PMID:30442668
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1552609	Marchf3	membrane associated ring-CH-type finger 3	gene	MP:0020148	abnormal susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20190110	MGI			PMID:30442668
1552610	Eif4a1	eukaryotic translation initiation factor 4A1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38011999
1552610	Eif4a1	eukaryotic translation initiation factor 4A1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20240627	MGI			PMID:38011999
1552610	Eif4a1	eukaryotic translation initiation factor 4A1	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38011999
1552610	Eif4a1	eukaryotic translation initiation factor 4A1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38011999
1552610	Eif4a1	eukaryotic translation initiation factor 4A1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:38011999
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20170105	MGI			
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20170105	MGI			
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600521
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584074
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0002885	abnormal AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0003063	increased coping response		IEA		N	RGD:5509061	20240523	MGI			
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20210520	MGI			
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600521
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10922077
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600521
1552611	Ppp1r9b	protein phosphatase 1, regulatory subunit 9B	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20201022	MGI			
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20201022	MGI			
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20201022	MGI			
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20201022	MGI			
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0002310	decreased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0002323	decreased susceptibility to hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19732742
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0009128	decreased brown fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19287392
1552612	Mogat2	monoacylglycerol O-acyltransferase 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1552615	Rpl32	ribosomal protein L32	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1552619	Grin3a	glutamate receptor ionotropic, NMDA3A	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1552619	Grin3a	glutamate receptor ionotropic, NMDA3A	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20200514	MGI			
1552619	Grin3a	glutamate receptor ionotropic, NMDA3A	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15866554
1552619	Grin3a	glutamate receptor ionotropic, NMDA3A	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620802
1552619	Grin3a	glutamate receptor ionotropic, NMDA3A	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14507892
1552619	Grin3a	glutamate receptor ionotropic, NMDA3A	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620802
1552620	Dnaaf1	dynein, axonemal assembly factor 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1552620	Dnaaf1	dynein, axonemal assembly factor 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552620	Dnaaf1	dynein, axonemal assembly factor 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552620	Dnaaf1	dynein, axonemal assembly factor 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552620	Dnaaf1	dynein, axonemal assembly factor 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552620	Dnaaf1	dynein, axonemal assembly factor 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552620	Dnaaf1	dynein, axonemal assembly factor 1	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20231207	MGI			
1552620	Dnaaf1	dynein, axonemal assembly factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552620	Dnaaf1	dynein, axonemal assembly factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1552621	Cnot1	CCR4-NOT transcription complex, subunit 1	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20200310	MGI			PMID:29438013
1552621	Cnot1	CCR4-NOT transcription complex, subunit 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:29438013
1552621	Cnot1	CCR4-NOT transcription complex, subunit 1	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29438013
1552621	Cnot1	CCR4-NOT transcription complex, subunit 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29438013
1552625	Nmur1	neuromedin U receptor 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:17379411
1552625	Nmur1	neuromedin U receptor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:19070594
1552625	Nmur1	neuromedin U receptor 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20200310	MGI			PMID:16474416
1552625	Nmur1	neuromedin U receptor 1	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18941143
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12644704
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0005469	abnormal thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004031
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0005472	abnormal triiodothyronine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004031
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340055
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376703
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677425
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:11057673
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12376703
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12644704
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004031
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677425
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0008875	abnormal xenobiotic pharmacokinetics		IAGP		N	RGD:5509061	20141003	MGI			PMID:18677425
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15004031
1552629	Nr1i3	nuclear receptor subfamily 1, group I, member 3	gene	MP:0010951	abnormal lipid oxidation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18941143
1552631	Skp2	S-phase kinase-associated protein 2	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790373
1552631	Skp2	S-phase kinase-associated protein 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790373
1552631	Skp2	S-phase kinase-associated protein 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11861371
1552631	Skp2	S-phase kinase-associated protein 2	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790373
1552631	Skp2	S-phase kinase-associated protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790373
1552631	Skp2	S-phase kinase-associated protein 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10790373
1552631	Skp2	S-phase kinase-associated protein 2	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818378
1552631	Skp2	S-phase kinase-associated protein 2	gene	MP:0008755	abnormal immunoglobulin V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349429
1552631	Skp2	S-phase kinase-associated protein 2	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:10790373
1552632	Cd320	CD320 antigen	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23430977
1552632	Cd320	CD320 antigen	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23430977
1552632	Cd320	CD320 antigen	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20200310	MGI			
1552632	Cd320	CD320 antigen	gene	MP:0004019	abnormal vitamin homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23430977
1552632	Cd320	CD320 antigen	gene	MP:0011227	abnormal vitamin B12 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23430977
1552632	Cd320	CD320 antigen	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1552632	Cd320	CD320 antigen	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23430977
1552632	Cd320	CD320 antigen	gene	MP:0030628	increased methylmalonic acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23430977
1552632	Cd320	CD320 antigen	gene	MP:0030630	increased circulating methylmalonic acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23430977
1552634	Tspan11	tetraspanin 11	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20210128	MGI			
1552634	Tspan11	tetraspanin 11	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20210128	MGI			
1552636	Kcnk18	potassium channel, subfamily K, member 18	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1552636	Kcnk18	potassium channel, subfamily K, member 18	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962323
1552636	Kcnk18	potassium channel, subfamily K, member 18	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962323
1552636	Kcnk18	potassium channel, subfamily K, member 18	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20170105	MGI			
1552636	Kcnk18	potassium channel, subfamily K, member 18	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17962323
1552637	Zbtb4	zinc finger and BTB domain containing 4	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20200310	MGI			
1552637	Zbtb4	zinc finger and BTB domain containing 4	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1552637	Zbtb4	zinc finger and BTB domain containing 4	gene	MP:0001307	fused cornea and lens		IEA		N	RGD:5509061	20200310	MGI			
1552637	Zbtb4	zinc finger and BTB domain containing 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1552637	Zbtb4	zinc finger and BTB domain containing 4	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1552637	Zbtb4	zinc finger and BTB domain containing 4	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1552637	Zbtb4	zinc finger and BTB domain containing 4	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20201231	MGI			
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421483
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340140
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0000962	disorganized dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875122
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875122
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12004056
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340140
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421483
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074277
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875122
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340140
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421483
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0002963	decreased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875122
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421483
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421483
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421483
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0010079	increased osteochondroma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421483
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0010280	increased skeletal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421483
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0010280	increased skeletal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20940146
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:16155866
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0010971	abnormal periosteum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421483
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875122
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552640	Prkaca	protein kinase, cAMP dependent, catalytic, alpha	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11886853
1552646	Or5an6	olfactory receptor family 5 subfamily AN member 6	gene	MP:0020852	abnormal olfactory behavior		IAGP		N	RGD:5509061	20200917	MGI			PMID:30643144
1552647	Wdr12	WD repeat domain 12	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170105	MGI			
1552647	Wdr12	WD repeat domain 12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552647	Wdr12	WD repeat domain 12	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552647	Wdr12	WD repeat domain 12	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552648	Ankib1	ankyrin repeat and IBR domain containing 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20200310	MGI			
1552648	Ankib1	ankyrin repeat and IBR domain containing 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1552648	Ankib1	ankyrin repeat and IBR domain containing 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1552648	Ankib1	ankyrin repeat and IBR domain containing 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1552648	Ankib1	ankyrin repeat and IBR domain containing 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20200310	MGI			
1552649	Fstl4	follistatin-like 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:18253481
1552650	Acvr1c	activin A receptor, type IC	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210826	MGI			
1552650	Acvr1c	activin A receptor, type IC	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485907
1552650	Acvr1c	activin A receptor, type IC	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564040
1552650	Acvr1c	activin A receptor, type IC	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20201022	MGI			
1552650	Acvr1c	activin A receptor, type IC	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0003608	prostate gland inflammation		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0005305	prostate gland anterior lobe hyperplasia		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0009219	increased prostate intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0009381	abnormal prostate gland dorsolateral lobe morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20230223	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0013320	dilated seminal vesicle		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0013899	abnormal seminal vesicle epithelium morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:30126926
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0031369	prostate gland dorsolateral lobe hyperplasia		IAGP		N	RGD:5509061	20231109	MGI			PMID:37093546
1552652	Elac2	elaC ribonuclease Z 2	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260709	MGI			PMID:30126926
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20240926	MGI			PMID:33219327
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20240926	MGI			PMID:33219327
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20240926	MGI			PMID:33219327
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20240926	MGI			PMID:33219327
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0002649	abnormal enamel rod pattern		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20240926	MGI			PMID:33219327
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20240926	MGI			PMID:33219327
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0004831	long incisors		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0011416	abnormal testis interstitial tissue morphology		IAGP		N	RGD:5509061	20240926	MGI			PMID:33219327
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20240926	MGI			PMID:33219327
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0030459	abnormal tooth attrition		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0030471	abnormal ameloblast differentiation		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0030541	misaligned incisors		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552653	Mast4	microtubule associated serine/threonine kinase family member 4	gene	MP:0030544	abnormal enamel development		IAGP		N	RGD:5509061	20250116	MGI			PMID:38945953
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20191017	MGI			PMID:27032083
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20191017	MGI			PMID:27032083
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20191017	MGI			PMID:27032083
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20191017	MGI			PMID:27032083
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:27032083
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20191017	MGI			PMID:27032083
1552654	Pdgfd	platelet-derived growth factor, D polypeptide	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20191017	MGI			PMID:27032083
1552656	Clec14a	C-type lectin domain family 14, member a	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20200310	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0000458	abnormal mandible morphology		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20160804	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0005358	abnormal incisor morphology		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20160804	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20141003	MGI			
1552659	Slc25a21	solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20141003	MGI			
1552660	Chmp4b	charged multivesicular body protein 4B	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17683935
1552661	Cpa5	carboxypeptidase A5	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20220519	MGI			
1552661	Cpa5	carboxypeptidase A5	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1552661	Cpa5	carboxypeptidase A5	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20220519	MGI			
1552665	Snx11	sorting nexin 11	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20260402	MGI			
1552665	Snx11	sorting nexin 11	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20210923	MGI			PMID:31730264
1552665	Snx11	sorting nexin 11	gene	MP:0003663	abnormal thermosensation		IAGP		N	RGD:5509061	20210923	MGI			PMID:31730264
1552665	Snx11	sorting nexin 11	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1552665	Snx11	sorting nexin 11	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20210923	MGI			PMID:31730264
1552665	Snx11	sorting nexin 11	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1552667	Desi2	desumoylating isopeptidase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21553223
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000537	abnormal urethra morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000909	abnormal facial motor nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000958	peripheral nervous system degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001334	absent optic tract		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20220519	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001948	vesicoureteral reflux		IAGP		N	RGD:5509061	20240926	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210826	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20220519	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0003624	anuria		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0008492	dorsal root ganglion degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0010057	abnormal olfactory bulb outer nerve layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23082226
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552668	Nmnat2	nicotinamide nucleotide adenylyltransferase 2	gene	MP:0012484	decreased corticospinal tract size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23946398
1552671	Phtf1	putative homeodomain transcription factor 1	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20181227	MGI			
1552671	Phtf1	putative homeodomain transcription factor 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1552673	Gpc4	glypican 4	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20240523	MGI			
1552673	Gpc4	glypican 4	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20230601	MGI			
1552673	Gpc4	glypican 4	gene	MP:0001577	anemia		IEA		N	RGD:5509061	20141003	MGI			
1552673	Gpc4	glypican 4	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20240523	MGI			
1552673	Gpc4	glypican 4	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1552673	Gpc4	glypican 4	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20240523	MGI			
1552673	Gpc4	glypican 4	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1552673	Gpc4	glypican 4	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20240523	MGI			
1552673	Gpc4	glypican 4	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1552673	Gpc4	glypican 4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1552673	Gpc4	glypican 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1552673	Gpc4	glypican 4	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:12376353
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12376353
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:12376353
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:12740217
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12060563
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126996
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11867335
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12376353
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:11237812
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:17967856
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:9126996
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12060563
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12376353
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16917077
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11867335
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12060563
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16917077
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9700084
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12376353
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11867335
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11867335
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11867335
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0010895	increased lung compliance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12740217
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12376353
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11867335
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17967856
1552674	Sftpa1	surfactant associated protein A1	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11867335
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19564410
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11390367
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20679483
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17875667
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17875667
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19564410
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19564410
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17875667
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19564410
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:17875667
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:20679483
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20679483
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:20679483
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19564410
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20679483
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:14515362
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20200310	MGI			PMID:11562351
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20679483
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:20679483
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19564410
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11390367
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:20679483
1552682	Mapk8ip1	mitogen-activated protein kinase 8 interacting protein 1	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:20679483
1552685	Vps16	VSP16 CORVET/HOPS core subunit	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20180301	MGI			PMID:27174565
1552685	Vps16	VSP16 CORVET/HOPS core subunit	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20180301	MGI			PMID:27174565
1552686	Or4e5	olfactory receptor family 4 subfamily E member 5	gene	MP:0001003	abnormal olfactory receptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24120133
1552686	Or4e5	olfactory receptor family 4 subfamily E member 5	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15157418
1552687	Sfxn3	sideroflexin 3	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20241121	MGI			
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20231207	MGI			
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0003325	decreased liver function		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552689	Degs1	delta 4-desaturase, sphingolipid 1	gene	MP:0030021	increased muscle cell glucose uptake		IAGP		N	RGD:5509061	20200310	MGI			PMID:17339025
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0010332	abnormal circulating apolipoprotein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0010333	abnormal circulating apolipoprotein E level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0011738	anasarca		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479625
1552696	Bpnt1	3'(2'), 5'-bisphosphate nucleotidase 1	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:23479625
1552701	Nufip1	nuclear FMR1 interacting protein 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20230119	MGI			PMID:35982178
1552701	Nufip1	nuclear FMR1 interacting protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552701	Nufip1	nuclear FMR1 interacting protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220811	MGI			
1552701	Nufip1	nuclear FMR1 interacting protein 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1552701	Nufip1	nuclear FMR1 interacting protein 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1552703	Kif5b	kinesin family member 5B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657148
1552703	Kif5b	kinesin family member 5B	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657148
1552703	Kif5b	kinesin family member 5B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657148
1552703	Kif5b	kinesin family member 5B	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657148
1552703	Kif5b	kinesin family member 5B	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:21335237
1552703	Kif5b	kinesin family member 5B	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:20870970
1552703	Kif5b	kinesin family member 5B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9657148
1552703	Kif5b	kinesin family member 5B	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21335237
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000117	absent tooth placode		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20250508	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20241121	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20241121	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20241121	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24784881
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24784881
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20250508	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20250508	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0002102	abnormal ear morphology		IEA		N	RGD:5509061	20250508	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20250508	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0002177	abnormal outer ear morphology		IEA		N	RGD:5509061	20250508	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20200310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0003104	acrania		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20250508	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20200310	MGI			PMID:24784881
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004383	absent interparietal bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004419	absent parietal bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004443	absent supraoccipital bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004445	small exoccipital bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004447	small basioccipital bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004872	absent nasal septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0004913	absent mandibular angle		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0006418	abnormal testis cord formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24784881
1552712	Hhat	hedgehog acyltransferase	gene	MP:0008274	failure of bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0009846	abnormal neural crest morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0010043	abnormal frontonasal suture morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0010939	abnormal mandibular prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20250508	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20250508	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0012092	diencephalon hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0012247	absent cornea		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0013523	increased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20241121	MGI			
1552712	Hhat	hedgehog acyltransferase	gene	MP:0013603	abnormal fetal Leydig cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24784881
1552712	Hhat	hedgehog acyltransferase	gene	MP:0013818	abnormal oral cavity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0021104	abnormal ventral interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0021105	abnormal ventral interneuron 3 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:15075292
1552712	Hhat	hedgehog acyltransferase	gene	MP:0030200	abnormal nasal septum cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14975718
1552712	Hhat	hedgehog acyltransferase	gene	MP:0030249	small frontonasal prominence		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0030268	agnathia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0031449	abnormal nasal cartilage morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:23055936
1552712	Hhat	hedgehog acyltransferase	gene	MP:0031450	nasal cartilage hypoplasia		IAGP		N	RGD:5509061	20221110	MGI			PMID:23055936
1552714	Cmtm2a	CKLF-like MARVEL transmembrane domain containing 2A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20190926	MGI			PMID:30209135
1552714	Cmtm2a	CKLF-like MARVEL transmembrane domain containing 2A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190926	MGI			PMID:30209135
1552714	Cmtm2a	CKLF-like MARVEL transmembrane domain containing 2A	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20190926	MGI			PMID:30209135
1552714	Cmtm2a	CKLF-like MARVEL transmembrane domain containing 2A	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20200102	MGI			PMID:30209135
1552716	Dnm1	dynamin 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0001499	abnormal kindling response		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0001650	abnormal seizure response to electrical stimulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
1552716	Dnm1	dynamin 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1552716	Dnm1	dynamin 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:27363778
1552716	Dnm1	dynamin 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
1552716	Dnm1	dynamin 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:27363778
1552716	Dnm1	dynamin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
1552716	Dnm1	dynamin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:20059951
1552716	Dnm1	dynamin 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25417109
1552716	Dnm1	dynamin 1	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1552716	Dnm1	dynamin 1	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
1552716	Dnm1	dynamin 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20059951
1552716	Dnm1	dynamin 1	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25417109
1552716	Dnm1	dynamin 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
1552716	Dnm1	dynamin 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
1552716	Dnm1	dynamin 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552716	Dnm1	dynamin 1	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20200310	MGI			PMID:21689597
1552716	Dnm1	dynamin 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0014254	increased paired-pulse ratio		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
1552716	Dnm1	dynamin 1	gene	MP:0014373	increased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0014384	increased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0014620	abnormal interictal brain wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:27363778
1552716	Dnm1	dynamin 1	gene	MP:0014740	increased auditory brainstem response wave peak latency		IAGP		N	RGD:5509061	20250911	MGI			PMID:20700442
1552716	Dnm1	dynamin 1	gene	MP:0031333	decreased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:17463283
1552716	Dnm1	dynamin 1	gene	MP:0031334	increased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:39127888
1552716	Dnm1	dynamin 1	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:20700442
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:11961557
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:12707359
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:19088190
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:21494554
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12707359
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18493980
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12707359
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12707359
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11961557
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:16148148
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12707359
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008471	abnormal spleen primary B follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:12707359
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:12707359
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21494554
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:10708458
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21494554
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18493980
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:12707359
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14597717
1552719	Ifnb1	interferon beta 1, fibroblast	gene	MP:0020928	increased susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:10708458
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20240613	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32619401
1552725	Dnah8	dynein, axonemal, heavy chain 8	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:32619401
1552726	Dhh	desert hedgehog	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8805249
1552726	Dhh	desert hedgehog	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8805249
1552726	Dhh	desert hedgehog	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8805249
1552726	Dhh	desert hedgehog	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8805249
1552726	Dhh	desert hedgehog	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8805249
1552726	Dhh	desert hedgehog	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8805249
1552726	Dhh	desert hedgehog	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0002789	male pseudohermaphroditism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482238
1552726	Dhh	desert hedgehog	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8805249
1552726	Dhh	desert hedgehog	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0006418	abnormal testis cord formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0006420	abnormal peritubular myoid cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0006421	decreased number of peritubular myoid cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8805249
1552726	Dhh	desert hedgehog	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:11090455
1552726	Dhh	desert hedgehog	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:8805249
1552731	Or10j5	olfactory receptor family 10 subfamily J member 5	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194868
1552731	Or10j5	olfactory receptor family 10 subfamily J member 5	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537788
1552731	Or10j5	olfactory receptor family 10 subfamily J member 5	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353676
1552731	Or10j5	olfactory receptor family 10 subfamily J member 5	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18353676
1552731	Or10j5	olfactory receptor family 10 subfamily J member 5	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12194868
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20200514	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20200514	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20200514	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20221215	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20200514	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0008725	increased heart atrium size		IEA		N	RGD:5509061	20200514	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0013510	decreased CD4-negative NK T cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0013513	decreased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0013649	decreased CD11b-high dendritic cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0013678	decreased Ly6C-positive NK T cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0013679	increased Ly6C-positive NK T cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0013691	decreased CD5-positive Ly6C-positive T cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20210520	MGI			
1552732	Nub1	negative regulator of ubiquitin-like proteins 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15486564
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:15486564
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15486564
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15486564
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17554336
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18159219
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22948941
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15486564
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24504341
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15486564
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:9814708
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21474102
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22020437
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15486564
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0011091	prenatal lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9814708
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:15486564
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24504341
1552733	Pou5f1	POU domain, class 5, transcription factor 1	gene	MP:0011411	abnormal gonadal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15486564
1552735	Krt9	keratin 9	gene	MP:0000574	abnormal foot pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0001188	hyperpigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0001236	abnormal epidermis stratum spinosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20220519	MGI			
1552735	Krt9	keratin 9	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552735	Krt9	keratin 9	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23962810
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11239162
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265900
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11239162
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265900
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19401562
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265900
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265900
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265900
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11239162
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19401562
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15265900
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11239162
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19401562
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:11239162
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19401562
1552736	Grap2	GRB2-related adaptor protein 2	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19401562
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20210121	MGI			PMID:32876667
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282321
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210121	MGI			PMID:32876667
1552737	Ubr5	ubiquitin protein ligase E3 component n-recognin 5	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:15282321
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220811	MGI			
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20220811	MGI			
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0005390	skeleton phenotype		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0010768	mortality/aging		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1552738	Pdk1	pyruvate dehydrogenase kinase, isoenzyme 1	gene	MP:0013404	decreased circulating lactate level		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1552741	Rnase9	ribonuclease, RNase A family, 9 (non-active)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:24719258
1552741	Rnase9	ribonuclease, RNase A family, 9 (non-active)	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20160526	MGI			PMID:24719258
1552741	Rnase9	ribonuclease, RNase A family, 9 (non-active)	gene	MP:0003666	impaired sperm capacitation		IAGP		N	RGD:5509061	20160526	MGI			PMID:24719258
1552742	Ipmk	inositol polyphosphate multikinase	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:15939867
1552742	Ipmk	inositol polyphosphate multikinase	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:15939867
1552742	Ipmk	inositol polyphosphate multikinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15939867
1552742	Ipmk	inositol polyphosphate multikinase	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:15939867
1552742	Ipmk	inositol polyphosphate multikinase	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:15939867
1552742	Ipmk	inositol polyphosphate multikinase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15939867
1552742	Ipmk	inositol polyphosphate multikinase	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15939867
1552742	Ipmk	inositol polyphosphate multikinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15939867
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15103023
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17241289
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574394
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:15103023
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:15103023
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15103023
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574394
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574394
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:17241289
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17241289
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002801	abnormal long-term object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:17241289
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:15103023
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19574394
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0003444	abnormal neurotransmitter uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:15103023
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15103023
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:15118123
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0020340	abnormal inhibitory learning		IAGP		N	RGD:5509061	20160915	MGI			PMID:19574394
1552743	Slc17a7	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230119	MGI			
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16283624
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16283624
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16283624
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10430909
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10430909
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417405
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716689
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10430909
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417405
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16283624
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:10430909
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0003895	increased ectoderm apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10430909
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0003895	increased ectoderm apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417405
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0003950	abnormal plasma membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10430909
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10430909
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0004193	abnormal kidney papilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716689
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716689
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0009350	decreased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716689
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716689
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16109770
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10430909
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417405
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1552745	Ugcg	UDP-glucose ceramide glucosyltransferase	gene	MP:0011736	decreased urine ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716689
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20200310	MGI			
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20210318	MGI			PMID:33238133
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0006038	increased mitochondrial fission		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20210318	MGI			PMID:33238133
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20210318	MGI			PMID:33238133
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IAGP		N	RGD:5509061	20210318	MGI			PMID:33238133
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0014788	decreased protein level		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0014956	decreased mitochondria enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0014961	increased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0014985	decreased cytochrome-c oxidase activity		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552746	Gfm1	G elongation factor, mitochondrial 1	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260716	MGI			PMID:34919756
1552748	Mphosph10	M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1552748	Mphosph10	M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20240523	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18424734
1552750	Masp1	MBL associated serine protease 1	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20240523	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20240523	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20260402	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0002472	impaired complement alternative pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943708
1552750	Masp1	MBL associated serine protease 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20240523	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18424734
1552750	Masp1	MBL associated serine protease 1	gene	MP:0009062	impaired lectin complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:18424734
1552750	Masp1	MBL associated serine protease 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552750	Masp1	MBL associated serine protease 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1552754	Scly	selenocysteine lyase	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22487427
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0008600	decreased circulating interleukin-2 level		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552755	Nmt2	N-myristoyltransferase 2	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20151203	MGI			PMID:26423150
1552756	Ddx59	DEAD box helicase 59	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1552756	Ddx59	DEAD box helicase 59	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191205	MGI			
1552756	Ddx59	DEAD box helicase 59	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1552756	Ddx59	DEAD box helicase 59	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1552756	Ddx59	DEAD box helicase 59	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20170504	MGI			
1552756	Ddx59	DEAD box helicase 59	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1552756	Ddx59	DEAD box helicase 59	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1552756	Ddx59	DEAD box helicase 59	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552756	Ddx59	DEAD box helicase 59	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1552756	Ddx59	DEAD box helicase 59	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241128	MGI			
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15887119
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15887119
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15887119
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0003978	decreased circulating carnitine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15887119
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:11390422
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:15887119
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0020963	decreased c-wave amplitude		IAGP		N	RGD:5509061	20250821	MGI			PMID:37644104
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:15887119
1552757	Hadha	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:15887119
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876643
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876643
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001717	absent ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876643
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876643
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0003817	abnormal pituitary diverticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876643
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876643
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876643
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20876643
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14729950
1552758	Pou2f1	POU domain, class 2, transcription factor 1	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:14729950
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25822906
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25819842
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863714
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:25819842
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0002630	abnormal endocochlear potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0003151	absent tunnel of Corti		IAGP		N	RGD:5509061	20200310	MGI			PMID:25819842
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25822906
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25819842
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25822906
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25822906
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:25822906
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23863714
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20200310	MGI			
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:25217574
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:25819842
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:25822906
1552760	Ildr1	immunoglobulin-like domain containing receptor 1	gene	MP:0013808	abnormal tunnel of Corti morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25819842
1552761	Msrb3	methionine sulfoxide reductase B3	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:24191262
1552761	Msrb3	methionine sulfoxide reductase B3	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24191262
1552761	Msrb3	methionine sulfoxide reductase B3	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24191262
1552761	Msrb3	methionine sulfoxide reductase B3	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24191262
1552761	Msrb3	methionine sulfoxide reductase B3	gene	MP:0004530	absent outer hair cell stereocilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24191262
1552761	Msrb3	methionine sulfoxide reductase B3	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24191262
1552761	Msrb3	methionine sulfoxide reductase B3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:24191262
1552763	Dmxl1	Dmx-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260326	MGI			PMID:41330162
1552763	Dmxl1	Dmx-like 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:41330162
1552763	Dmxl1	Dmx-like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666675
1552765	Itgb6	integrin beta 6	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666675
1552765	Itgb6	integrin beta 6	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12634787
1552765	Itgb6	integrin beta 6	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666675
1552765	Itgb6	integrin beta 6	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9761761
1552765	Itgb6	integrin beta 6	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666675
1552765	Itgb6	integrin beta 6	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12634787
1552765	Itgb6	integrin beta 6	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353357
1552765	Itgb6	integrin beta 6	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12634787
1552765	Itgb6	integrin beta 6	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:12634787
1552765	Itgb6	integrin beta 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20240627	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8666675
1552765	Itgb6	integrin beta 6	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9761761
1552765	Itgb6	integrin beta 6	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:14507636
1552765	Itgb6	integrin beta 6	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:14507636
1552765	Itgb6	integrin beta 6	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20250508	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0008118	absent Langerhans cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353357
1552765	Itgb6	integrin beta 6	gene	MP:0008119	decreased Langerhans cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353357
1552765	Itgb6	integrin beta 6	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0010895	increased lung compliance		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0011045	decreased lung elastance		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0011048	decreased lung tissue damping		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20230119	MGI			
1552765	Itgb6	integrin beta 6	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20250508	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210520	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210826	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210826	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20201022	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20201022	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20210520	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1552768	Nucb1	nucleobindin 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1552771	Tmem14a	transmembrane protein 14A	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1552773	Ubac1	ubiquitin associated domain containing 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1552773	Ubac1	ubiquitin associated domain containing 1	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1552773	Ubac1	ubiquitin associated domain containing 1	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1552773	Ubac1	ubiquitin associated domain containing 1	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20201022	MGI			
1552773	Ubac1	ubiquitin associated domain containing 1	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20201022	MGI			
1552773	Ubac1	ubiquitin associated domain containing 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1552773	Ubac1	ubiquitin associated domain containing 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1552773	Ubac1	ubiquitin associated domain containing 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1552776	Ldhc	lactate dehydrogenase C	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367675
1552776	Ldhc	lactate dehydrogenase C	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367675
1552776	Ldhc	lactate dehydrogenase C	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367675
1552776	Ldhc	lactate dehydrogenase C	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367675
1552776	Ldhc	lactate dehydrogenase C	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367675
1552776	Ldhc	lactate dehydrogenase C	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367675
1552777	Tspyl1	testis-specific protein, Y-encoded-like 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1552777	Tspyl1	testis-specific protein, Y-encoded-like 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1552777	Tspyl1	testis-specific protein, Y-encoded-like 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1552777	Tspyl1	testis-specific protein, Y-encoded-like 1	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20201022	MGI			
1552777	Tspyl1	testis-specific protein, Y-encoded-like 1	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20240523	MGI			
1552777	Tspyl1	testis-specific protein, Y-encoded-like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552780	Eva1c	eva-1 homolog C	gene	MP:0002638	abnormal pupillary reflex		IEA		N	RGD:5509061	20170323	MGI			
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20210128	MGI			
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18187333
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535435
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15799973
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18187333
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:24075852
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:18187333
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18187333
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17560790
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15799973
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20241121	MGI			
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721235
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17560790
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15799973
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24075852
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20150319	MGI			PMID:23019375
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721235
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15799973
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18187333
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20241121	MGI			
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20150319	MGI			PMID:23019375
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20150319	MGI			PMID:23019375
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535435
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0003444	abnormal neurotransmitter uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721235
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:23019375
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:23019375
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721235
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721235
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28360124
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0008830	abnormal nucleolus morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:28360124
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15784737
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15784737
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:18187333
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20150319	MGI			PMID:23019375
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24075852
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17766438
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17766438
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17560790
1552781	Park7	Parkinson disease (autosomal recessive, early onset) 7	gene	MP:0013219	abnormal substantia nigra pars compacta morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:23019375
1552783	Ubb	ubiquitin B	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552783	Ubb	ubiquitin B	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552783	Ubb	ubiquitin B	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20191107	MGI			PMID:30935687
1552783	Ubb	ubiquitin B	gene	MP:0001697	abnormal embryo size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552783	Ubb	ubiquitin B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552783	Ubb	ubiquitin B	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552783	Ubb	ubiquitin B	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20191107	MGI			PMID:30935687
1552783	Ubb	ubiquitin B	gene	MP:0008453	decreased retina rod cell number		IAGP		N	RGD:5509061	20191107	MGI			PMID:30935687
1552783	Ubb	ubiquitin B	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20191107	MGI			PMID:30935687
1552783	Ubb	ubiquitin B	gene	MP:0009363	abnormal tertiary ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0009375	thin zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1552783	Ubb	ubiquitin B	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299572
1552783	Ubb	ubiquitin B	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20150312	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0014447	impaired spindle assembly in female meiosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:18070917
1552783	Ubb	ubiquitin B	gene	MP:0031422	failure of superovulation		IAGP		N	RGD:5509061	20220630	MGI			PMID:18070917
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0000525	renal tubular acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020613
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020613
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020613
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020613
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281477
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020613
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281477
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281477
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0005628	decreased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020613
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020613
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281477
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281477
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0011736	decreased urine ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020613
1552784	Rhcg	Rh family C glycoprotein	gene	MP:0011736	decreased urine ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281477
1552785	Panx3	pannexin 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20160825	MGI			PMID:26138248
1552785	Panx3	pannexin 3	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20160825	MGI			PMID:26138248
1552785	Panx3	pannexin 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1552785	Panx3	pannexin 3	gene	MP:0013304	osteophytes		IAGP		N	RGD:5509061	20160825	MGI			PMID:26138248
1552786	Aox4	aldehyde oxidase 4	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18981221
1552786	Aox4	aldehyde oxidase 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18981221
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000071	axial skeleton hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20160505	MGI			PMID:25126760
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056490
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986259
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986259
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20160505	MGI			PMID:25126760
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986259
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986259
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986259
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25126760
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986259
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004266	pale placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004447	small basioccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20160505	MGI			PMID:25126760
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004572	fusion of basioccipital and basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20160505	MGI			PMID:25126760
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20160505	MGI			PMID:25126760
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0009384	cardiac valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0009912	decreased hyoid bone size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0010941	abnormal foramen magnum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0010987	abnormal nephrogenic mesenchyme morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986259
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011177	abnormal erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011292	absent nephron		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011366	absent metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011366	absent metanephros		IAGP		N	RGD:5509061	20160505	MGI			PMID:25126760
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19715689
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17986259
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0012251	abnormal diaphragm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0012514	pectus excavatum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0030279	thin neurocranium		IAGP		N	RGD:5509061	20171102	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0030872	small cricoid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0031574	thick atrioventricular valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:19383940
1552790	Fgfrl1	fibroblast growth factor receptor-like 1	gene	MP:0031584	thick semilunar valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:19383940
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509076
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509076
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509076
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509076
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0008655	decreased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509076
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509076
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24509076
1552792	Cxcl5	C-X-C motif chemokine ligand 5	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643340
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20230601	MGI			
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210826	MGI			
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23522044
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:23522044
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0002885	abnormal AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:23522044
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:23522044
1552794	Cnih2	cornichon family AMPA receptor auxiliary protein 2	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:23522044
1552798	Brinp2	bone morphogenic protein/retinoic acid inducible neural-specific 2	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20240523	MGI			
1552798	Brinp2	bone morphogenic protein/retinoic acid inducible neural-specific 2	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1552798	Brinp2	bone morphogenic protein/retinoic acid inducible neural-specific 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20241121	MGI			
1552800	Reg3g	regenerating islet-derived 3 gamma	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20150108	MGI			
1552800	Reg3g	regenerating islet-derived 3 gamma	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20150108	MGI			
1552800	Reg3g	regenerating islet-derived 3 gamma	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998396
1552800	Reg3g	regenerating islet-derived 3 gamma	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998396
1552800	Reg3g	regenerating islet-derived 3 gamma	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20150108	MGI			
1552800	Reg3g	regenerating islet-derived 3 gamma	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998396
1552800	Reg3g	regenerating islet-derived 3 gamma	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998396
1552800	Reg3g	regenerating islet-derived 3 gamma	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998396
1552800	Reg3g	regenerating islet-derived 3 gamma	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:26329040
1552802	Syt17	synaptotagmin XVII	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1552802	Syt17	synaptotagmin XVII	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1552802	Syt17	synaptotagmin XVII	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20200310	MGI			
1552802	Syt17	synaptotagmin XVII	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1552802	Syt17	synaptotagmin XVII	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1552802	Syt17	synaptotagmin XVII	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1552802	Syt17	synaptotagmin XVII	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20231207	MGI			
1552802	Syt17	synaptotagmin XVII	gene	MP:0005573	increased pulmonary respiratory rate		IEA		N	RGD:5509061	20210128	MGI			
1552802	Syt17	synaptotagmin XVII	gene	MP:0005574	decreased pulmonary respiratory rate		IEA		N	RGD:5509061	20260402	MGI			
1552802	Syt17	synaptotagmin XVII	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252120
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252120
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485893
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0001388	abnormal stationary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252120
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252120
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252120
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252120
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884661
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0003851	skeletal muscle interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252120
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252120
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884661
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0010052	increased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884661
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884661
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10485893
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12609501
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20260702	MGI			PMID:31582396
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15252120
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0012059	thick diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732288
1552804	Sgcg	sarcoglycan, gamma (dystrophin-associated glycoprotein)	gene	MP:0031192	coronary artery spasm		IAGP		N	RGD:5509061	20201119	MGI			PMID:14982859
1552805	Serping1	serine (or cysteine) peptidase inhibitor, clade G, member 1	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20210520	MGI			
1552805	Serping1	serine (or cysteine) peptidase inhibitor, clade G, member 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
1552805	Serping1	serine (or cysteine) peptidase inhibitor, clade G, member 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1552805	Serping1	serine (or cysteine) peptidase inhibitor, clade G, member 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210520	MGI			
1552805	Serping1	serine (or cysteine) peptidase inhibitor, clade G, member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956243
1552805	Serping1	serine (or cysteine) peptidase inhibitor, clade G, member 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1552805	Serping1	serine (or cysteine) peptidase inhibitor, clade G, member 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1552805	Serping1	serine (or cysteine) peptidase inhibitor, clade G, member 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1552805	Serping1	serine (or cysteine) peptidase inhibitor, clade G, member 1	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:11956243
1552806	Nubpl	nucleotide binding protein-like	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1552806	Nubpl	nucleotide binding protein-like	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1552806	Nubpl	nucleotide binding protein-like	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1552806	Nubpl	nucleotide binding protein-like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29539633
1552806	Nubpl	nucleotide binding protein-like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230413	MGI			PMID:36280881
1552806	Nubpl	nucleotide binding protein-like	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552806	Nubpl	nucleotide binding protein-like	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20170105	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20170105	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20170105	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0002176	increased brain weight		IEA		N	RGD:5509061	20241121	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20181227	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20210128	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0014787	increased protein level		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0020419	decreased cardiac muscle relaxation		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0021140	increased cardiac muscle calcium level		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552812	Gpld1	glycosylphosphatidylinositol specific phospholipase D1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20260716	MGI			PMID:40631685
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556505
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160211	MGI			PMID:24835669
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20160211	MGI			PMID:24835669
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556505
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556505
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160211	MGI			PMID:24835669
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0002892	decreased superior colliculus size		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0003246	loss of GABAergic neurons		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556505
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556505
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556505
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0009038	decreased inferior colliculus size		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0009960	abnormal cerebellum anterior lobe morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160211	MGI			PMID:24835669
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556505
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0011209	absent extraembryonic coelom		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556505
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12556505
1552813	Pelo	pelota mRNA surveillance and ribosome rescue factor	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20210715	MGI			PMID:33899734
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20201022	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20170105	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20201022	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0000576	clubfoot		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230601	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20170105	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20141003	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20170105	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002546	mydriasis		IEA		N	RGD:5509061	20230601	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230601	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0003757	high palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20201022	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20201022	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20230601	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20230601	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20230601	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0009874	abnormal interdigital cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0010714	iris coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0010715	retina coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0010772	abnormal pollex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21194678
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21750680
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20201022	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1552814	Smoc1	SPARC related modular calcium binding 1	gene	MP:0031291	pes valgus		IAGP		N	RGD:5509061	20211014	MGI			PMID:21194678
1552815	Miox	myo-inositol oxygenase	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:27895157
1552815	Miox	myo-inositol oxygenase	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:27895157
1552816	Krt33b	keratin 33B	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1552816	Krt33b	keratin 33B	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1552816	Krt33b	keratin 33B	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1552816	Krt33b	keratin 33B	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1552816	Krt33b	keratin 33B	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1552816	Krt33b	keratin 33B	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20210128	MGI			
1552816	Krt33b	keratin 33B	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552819	Aurka	aurora kinase A	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552819	Aurka	aurora kinase A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18345035
1552819	Aurka	aurora kinase A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220616	MGI			PMID:33901174
1552819	Aurka	aurora kinase A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20220616	MGI			PMID:33901174
1552819	Aurka	aurora kinase A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18345035
1552819	Aurka	aurora kinase A	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18345035
1552819	Aurka	aurora kinase A	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1552819	Aurka	aurora kinase A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18345035
1552819	Aurka	aurora kinase A	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18345035
1552819	Aurka	aurora kinase A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0004806	absent germ cells		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:18345035
1552819	Aurka	aurora kinase A	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0006204	embryonic lethality before implantation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18345035
1552819	Aurka	aurora kinase A	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:33901174
1552819	Aurka	aurora kinase A	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0009839	multiflagellated sperm		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0010767	abnormal female meiosis I arrest		IAGP		N	RGD:5509061	20220616	MGI			PMID:33901174
1552819	Aurka	aurora kinase A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18345035
1552819	Aurka	aurora kinase A	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19075002
1552819	Aurka	aurora kinase A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552819	Aurka	aurora kinase A	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0012121	sclerocornea		IEA		N	RGD:5509061	20200310	MGI			
1552819	Aurka	aurora kinase A	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:18801727
1552819	Aurka	aurora kinase A	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1552819	Aurka	aurora kinase A	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552819	Aurka	aurora kinase A	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220707	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0031427	increased sperm progressive motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:34518881
1552819	Aurka	aurora kinase A	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:19075002
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210520	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20160421	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20160811	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20170105	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20170105	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20170105	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20160421	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20160421	MGI			
1552820	Wsb2	WD repeat and SOCS box-containing 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20170105	MGI			
1552821	Golt1b	golgi transport 1B	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20210128	MGI			
1552821	Golt1b	golgi transport 1B	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1552821	Golt1b	golgi transport 1B	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1552821	Golt1b	golgi transport 1B	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1552821	Golt1b	golgi transport 1B	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20241121	MGI			
1552821	Golt1b	golgi transport 1B	gene	MP:0003393	decreased cardiac output		IEA		N	RGD:5509061	20200310	MGI			
1552821	Golt1b	golgi transport 1B	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1552821	Golt1b	golgi transport 1B	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20240523	MGI			
1552821	Golt1b	golgi transport 1B	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210128	MGI			
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552822	Mims1	mitochondrial inner membrane scaffold 1	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20180614	MGI			PMID:29618611
1552823	Or10a2	olfactory receptor family 10 subfamily A member 2	gene	MP:0012014	abnormal olfactory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15186781
1552824	Ankrd46	ankyrin repeat domain 46	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1552824	Ankrd46	ankyrin repeat domain 46	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20231207	MGI			
1552824	Ankrd46	ankyrin repeat domain 46	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20241121	MGI			
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:32649882
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20210422	MGI			PMID:32649882
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210422	MGI			PMID:32649882
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20210422	MGI			PMID:32649882
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210422	MGI			PMID:32649882
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:32649882
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20210422	MGI			PMID:32649882
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20210422	MGI			PMID:32649882
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0014040	increased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20210422	MGI			PMID:32649882
1552825	Vcpip1	valosin containing protein (p97)/p47 complex interacting protein 1	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:32649882
1552828	Nasp	nuclear autoantigenic sperm protein (histone-binding)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728391
1552828	Nasp	nuclear autoantigenic sperm protein (histone-binding)	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728391
1552828	Nasp	nuclear autoantigenic sperm protein (histone-binding)	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16728391
1552829	Ces2a	carboxylesterase 2A	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0014170	increased brown adipose tissue mass		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552829	Ces2a	carboxylesterase 2A	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20240912	MGI			PMID:37059417
1552832	Nme8	NME/NM23 family member 8	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1552832	Nme8	NME/NM23 family member 8	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1552832	Nme8	NME/NM23 family member 8	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1552832	Nme8	NME/NM23 family member 8	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1552832	Nme8	NME/NM23 family member 8	gene	MP:0012582	increased peroxidase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707457
1552833	Zng1	Zn regulated GTPase metalloprotein activator 1	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:31862704
1552833	Zng1	Zn regulated GTPase metalloprotein activator 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20220714	MGI			PMID:31862704
1552833	Zng1	Zn regulated GTPase metalloprotein activator 1	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20220714	MGI			PMID:31862704
1552833	Zng1	Zn regulated GTPase metalloprotein activator 1	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:31862704
1552833	Zng1	Zn regulated GTPase metalloprotein activator 1	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20260402	MGI			
1552833	Zng1	Zn regulated GTPase metalloprotein activator 1	gene	MP:0011425	abnormal kidney interstitium morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:31862704
1552833	Zng1	Zn regulated GTPase metalloprotein activator 1	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20220714	MGI			PMID:31862704
1552833	Zng1	Zn regulated GTPase metalloprotein activator 1	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1552833	Zng1	Zn regulated GTPase metalloprotein activator 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1552835	Drc3	dynein regulatory complex subunit 3	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552835	Drc3	dynein regulatory complex subunit 3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552835	Drc3	dynein regulatory complex subunit 3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552835	Drc3	dynein regulatory complex subunit 3	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552835	Drc3	dynein regulatory complex subunit 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552835	Drc3	dynein regulatory complex subunit 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23968836
1552838	Morc3	microrchidia 3	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17332504
1552838	Morc3	microrchidia 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552838	Morc3	microrchidia 3	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1552840	Eya2	EYA transcriptional coactivator and phosphatase 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1552840	Eya2	EYA transcriptional coactivator and phosphatase 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1552840	Eya2	EYA transcriptional coactivator and phosphatase 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1552840	Eya2	EYA transcriptional coactivator and phosphatase 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1552840	Eya2	EYA transcriptional coactivator and phosphatase 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20220428	MGI			PMID:33715274
1552840	Eya2	EYA transcriptional coactivator and phosphatase 2	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20220428	MGI			PMID:33715274
1552840	Eya2	EYA transcriptional coactivator and phosphatase 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1552840	Eya2	EYA transcriptional coactivator and phosphatase 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20220428	MGI			PMID:33715274
1552840	Eya2	EYA transcriptional coactivator and phosphatase 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20220428	MGI			PMID:33715274
1552846	Emp2	epithelial membrane protein 2	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20171207	MGI			PMID:28295343
1552846	Emp2	epithelial membrane protein 2	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:28295343
1552846	Emp2	epithelial membrane protein 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20171207	MGI			PMID:28295343
1552846	Emp2	epithelial membrane protein 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20171207	MGI			PMID:28295343
1552846	Emp2	epithelial membrane protein 2	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20171207	MGI			PMID:28295343
1552846	Emp2	epithelial membrane protein 2	gene	MP:0009394	increased uterine NK cell number		IAGP		N	RGD:5509061	20171207	MGI			PMID:28295343
1552846	Emp2	epithelial membrane protein 2	gene	MP:0012529	abnormal decidua basalis morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:28295343
1552850	Pgpep1	pyroglutamyl-peptidase I	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1552850	Pgpep1	pyroglutamyl-peptidase I	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1552851	Cyp4f13	cytochrome P450, family 4, subfamily f, polypeptide 13	gene	MP:0003192	increased cholesterol efflux		IAGP		N	RGD:5509061	20201002	MGI			PMID:31102955
1552851	Cyp4f13	cytochrome P450, family 4, subfamily f, polypeptide 13	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20201002	MGI			PMID:31102955
1552851	Cyp4f13	cytochrome P450, family 4, subfamily f, polypeptide 13	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20201002	MGI			PMID:31102955
1552851	Cyp4f13	cytochrome P450, family 4, subfamily f, polypeptide 13	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20201002	MGI			PMID:31102955
1552853	Rims4	regulating synaptic membrane exocytosis 4	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20260402	MGI			
1552853	Rims4	regulating synaptic membrane exocytosis 4	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20260402	MGI			
1552853	Rims4	regulating synaptic membrane exocytosis 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1552853	Rims4	regulating synaptic membrane exocytosis 4	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20180222	MGI			
1552853	Rims4	regulating synaptic membrane exocytosis 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1552853	Rims4	regulating synaptic membrane exocytosis 4	gene	MP:0003883	enlarged stomach		IEA		N	RGD:5509061	20260402	MGI			
1552853	Rims4	regulating synaptic membrane exocytosis 4	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20260402	MGI			
1552853	Rims4	regulating synaptic membrane exocytosis 4	gene	MP:0013129	abnormal tooth color		IEA		N	RGD:5509061	20260402	MGI			
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:2305264
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651535
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958830
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958830
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742101
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742101
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651535
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958830
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260219	MGI			PMID:38516887
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742101
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2305264
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260219	MGI			PMID:38516887
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20190516	MGI			PMID:28790031
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20260219	MGI			PMID:38516887
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032866
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002758	long tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002768	small adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958830
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002772	brachypodia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0002881	long hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0003415	priapism		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0003550	short perineum		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20260219	MGI			PMID:38516887
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032866
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742101
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958830
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742101
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12032866
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:14794889
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0008526	decreased cranium width		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:2305264
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958830
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0009105	penis prolapse		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0009151	increased pancreatic ductal adenocarcinoma incidence		IAGP		N	RGD:5509061	20190516	MGI			PMID:28790031
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742101
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10742101
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7651535
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20260219	MGI			PMID:38516887
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20260219	MGI			PMID:38516887
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552855	Hmga2	high mobility group AT-hook 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220714	MGI			PMID:34878116
1552857	Abca7	ATP-binding cassette, sub-family A member 7	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15550377
1552857	Abca7	ATP-binding cassette, sub-family A member 7	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15550377
1552857	Abca7	ATP-binding cassette, sub-family A member 7	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15550377
1552857	Abca7	ATP-binding cassette, sub-family A member 7	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1552857	Abca7	ATP-binding cassette, sub-family A member 7	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15550377
1552857	Abca7	ATP-binding cassette, sub-family A member 7	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220519	MGI			
1552857	Abca7	ATP-binding cassette, sub-family A member 7	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20211021	MGI			
1552857	Abca7	ATP-binding cassette, sub-family A member 7	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0001864	vascular inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002869	increased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008191	abnormal follicular B cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19299707
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14752163
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:21841778
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552858	Ptpn22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23619366
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20240201	MGI			PMID:37642681
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20240201	MGI			PMID:37642681
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20240201	MGI			PMID:37642681
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20240201	MGI			PMID:37642681
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20240201	MGI			PMID:37642681
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0013140	excessive vocalization		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0014345	abnormal neuron mitochondrial morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0020360	abnormal asymmetric synapse morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552859	Slc1a4	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	gene	MP:0021015	increased tau protein phosphorylation		IAGP		N	RGD:5509061	20260129	MGI			PMID:38662784
1552861	Ascc3	activating signal cointegrator 1 complex subunit 3	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20200310	MGI			
1552861	Ascc3	activating signal cointegrator 1 complex subunit 3	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20200310	MGI			
1552861	Ascc3	activating signal cointegrator 1 complex subunit 3	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20200310	MGI			
1552861	Ascc3	activating signal cointegrator 1 complex subunit 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1552862	Phc3	polyhomeotic 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1552864	Eif3h	eukaryotic translation initiation factor 3, subunit H	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1552864	Eif3h	eukaryotic translation initiation factor 3, subunit H	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173090
1552864	Eif3h	eukaryotic translation initiation factor 3, subunit H	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173090
1552864	Eif3h	eukaryotic translation initiation factor 3, subunit H	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1552864	Eif3h	eukaryotic translation initiation factor 3, subunit H	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173090
1552864	Eif3h	eukaryotic translation initiation factor 3, subunit H	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20141003	MGI			PMID:23173090
1552865	Entpd3	ectonucleoside triphosphate diphosphohydrolase 3	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20190815	MGI			PMID:25717362
1552865	Entpd3	ectonucleoside triphosphate diphosphohydrolase 3	gene	MP:0010073	decreased pruritus		IAGP		N	RGD:5509061	20190815	MGI			PMID:25717362
1552866	Oit3	oncoprotein induced transcript 3	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22306318
1552866	Oit3	oncoprotein induced transcript 3	gene	MP:0008822	decreased blood uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22306318
1552866	Oit3	oncoprotein induced transcript 3	gene	MP:0011424	decreased urine uric acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22306318
1552867	Per1	period circadian clock 1	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0001432	abnormal food preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15031135
1552867	Per1	period circadian clock 1	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267082
1552867	Per1	period circadian clock 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20150521	MGI			PMID:25673850
1552867	Per1	period circadian clock 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1552867	Per1	period circadian clock 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1552867	Per1	period circadian clock 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20150521	MGI			PMID:25673850
1552867	Per1	period circadian clock 1	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1552867	Per1	period circadian clock 1	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1552867	Per1	period circadian clock 1	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20150521	MGI			PMID:25673850
1552867	Per1	period circadian clock 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1552867	Per1	period circadian clock 1	gene	MP:0008961	abnormal basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18367514
1552867	Per1	period circadian clock 1	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20150521	MGI			PMID:25673850
1552867	Per1	period circadian clock 1	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15031135
1552867	Per1	period circadian clock 1	gene	MP:0011478	abnormal urine catecholamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1552867	Per1	period circadian clock 1	gene	MP:0014624	abnormal brain delta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:15031135
1552867	Per1	period circadian clock 1	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20171012	MGI			PMID:23267082
1552867	Per1	period circadian clock 1	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:15031135
1552867	Per1	period circadian clock 1	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:11483500
1552867	Per1	period circadian clock 1	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:11389837
1552867	Per1	period circadian clock 1	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:11395012
1552867	Per1	period circadian clock 1	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:15031135
1552867	Per1	period circadian clock 1	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:15888647
1552867	Per1	period circadian clock 1	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20171012	MGI			PMID:15888647
1552867	Per1	period circadian clock 1	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20171012	MGI			PMID:15031135
1552867	Per1	period circadian clock 1	gene	MP:0030438	increased osteoblast proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:16143109
1552867	Per1	period circadian clock 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25673850
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23712430
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19917682
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23712430
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17255932
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23712430
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20200310	MGI			PMID:17255932
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17255932
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:27503071
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19917682
1552868	Marchf1	membrane associated ring-CH-type finger 1	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19917682
1552869	Ankrd35	ankyrin repeat domain 35	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
1552870	Pnlip	pancreatic lipase	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915407
1552870	Pnlip	pancreatic lipase	gene	MP:0002647	decreased intestinal cholesterol absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
1552870	Pnlip	pancreatic lipase	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
1552870	Pnlip	pancreatic lipase	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
1552870	Pnlip	pancreatic lipase	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
1552870	Pnlip	pancreatic lipase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
1552870	Pnlip	pancreatic lipase	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
1552870	Pnlip	pancreatic lipase	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915407
1552870	Pnlip	pancreatic lipase	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
1552870	Pnlip	pancreatic lipase	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12915407
1552870	Pnlip	pancreatic lipase	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
1552870	Pnlip	pancreatic lipase	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17604277
1552870	Pnlip	pancreatic lipase	gene	MP:0014480	increased feces cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:12915407
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800625
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:20036347
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800624
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800624
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20036347
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15800625
1552871	Adamts5	ADAM metallopeptidase with thrombospondin type 1 motif 5	gene	MP:0009874	abnormal interdigital cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1552874	Fut7	fucosyltransferase 7	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982764
1552874	Fut7	fucosyltransferase 7	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16452210
1552874	Fut7	fucosyltransferase 7	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752218
1552874	Fut7	fucosyltransferase 7	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0002345	abnormal lymph node primary follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0002345	abnormal lymph node primary follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752218
1552874	Fut7	fucosyltransferase 7	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869507
1552874	Fut7	fucosyltransferase 7	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752218
1552874	Fut7	fucosyltransferase 7	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752218
1552874	Fut7	fucosyltransferase 7	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752218
1552874	Fut7	fucosyltransferase 7	gene	MP:0003627	abnormal leukocyte tethering or rolling		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752218
1552874	Fut7	fucosyltransferase 7	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752218
1552874	Fut7	fucosyltransferase 7	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308551
1552874	Fut7	fucosyltransferase 7	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535629
1552874	Fut7	fucosyltransferase 7	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859099
1552874	Fut7	fucosyltransferase 7	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11535629
1552874	Fut7	fucosyltransferase 7	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752218
1552874	Fut7	fucosyltransferase 7	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11485743
1552874	Fut7	fucosyltransferase 7	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:8752218
1552874	Fut7	fucosyltransferase 7	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10982764
1552874	Fut7	fucosyltransferase 7	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:11485743
1552877	Or1e32	olfactory receptor family 1 subfamily E member 32	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20230601	MGI			
1552877	Or1e32	olfactory receptor family 1 subfamily E member 32	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20230601	MGI			
1552877	Or1e32	olfactory receptor family 1 subfamily E member 32	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1552877	Or1e32	olfactory receptor family 1 subfamily E member 32	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1552877	Or1e32	olfactory receptor family 1 subfamily E member 32	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1552877	Or1e32	olfactory receptor family 1 subfamily E member 32	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1552877	Or1e32	olfactory receptor family 1 subfamily E member 32	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1552877	Or1e32	olfactory receptor family 1 subfamily E member 32	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20231207	MGI			
1552877	Or1e32	olfactory receptor family 1 subfamily E member 32	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20230601	MGI			
1552878	Prok2	prokineticin 2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976302
1552878	Prok2	prokineticin 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976302
1552878	Prok2	prokineticin 2	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15976302
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20181227	MGI			
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20151217	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20151217	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20151217	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20151217	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20151217	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0003326	liver failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20151217	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20151217	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20436477
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552880	Mtch2	mitochondrial carrier 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20160811	MGI			PMID:20923861
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20160811	MGI			PMID:20923861
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20160811	MGI			PMID:20923861
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0003288	intestinal edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20180111	MGI			PMID:28636595
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20160811	MGI			PMID:20923861
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0008136	enlarged Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0008896	increased IgG2c level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0011431	increased urine flow rate		IAGP		N	RGD:5509061	20160811	MGI			PMID:20923861
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0012306	enhanced spatial learning		IAGP		N	RGD:5509061	20160811	MGI			PMID:20923861
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20160811	MGI			PMID:20923861
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20160304	MGI			PMID:21593405
1552887	Nlrp6	NLR family, pyrin domain containing 6	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:28636595
1552891	Stk40	serine/threonine kinase 40	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0030002	increased lung apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552891	Stk40	serine/threonine kinase 40	gene	MP:0031006	increased lung glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23293024
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0008990	abnormal Ito cell morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20240530	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0020427	increased hepatocyte karyomegaly		IAGP		N	RGD:5509061	20221201	MGI			PMID:26458163
1552892	Ssu72	Ssu72 RNA polymerase II CTD phosphatase homolog (yeast)	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1552893	Lefty2	left-right determination factor 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0000542	left-sided isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0003284	abnormal large intestine placement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0003342	accessory spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0003872	absent heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0006123	tricuspid valve atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0008461	left atrial isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0010426	abnormal heart and great artery attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0010668	abnormal hepatic portal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11703930
1552893	Lefty2	left-right determination factor 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552893	Lefty2	left-right determination factor 2	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:10518210
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20160421	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20160421	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1552894	Ggps1	geranylgeranyl diphosphate synthase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552895	Cd1d1	CD1d1 antigen	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
1552895	Cd1d1	CD1d1 antigen	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552895	Cd1d1	CD1d1 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15958069
1552895	Cd1d1	CD1d1 antigen	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11550008
1552895	Cd1d1	CD1d1 antigen	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21921158
1552895	Cd1d1	CD1d1 antigen	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731798
1552895	Cd1d1	CD1d1 antigen	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339525
1552895	Cd1d1	CD1d1 antigen	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21921158
1552895	Cd1d1	CD1d1 antigen	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20171214	MGI			PMID:21964024
1552895	Cd1d1	CD1d1 antigen	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21921158
1552895	Cd1d1	CD1d1 antigen	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587020
1552895	Cd1d1	CD1d1 antigen	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1552895	Cd1d1	CD1d1 antigen	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0003076	increased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:21921158
1552895	Cd1d1	CD1d1 antigen	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15958069
1552895	Cd1d1	CD1d1 antigen	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552895	Cd1d1	CD1d1 antigen	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339525
1552895	Cd1d1	CD1d1 antigen	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
1552895	Cd1d1	CD1d1 antigen	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591216
1552895	Cd1d1	CD1d1 antigen	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591216
1552895	Cd1d1	CD1d1 antigen	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15591216
1552895	Cd1d1	CD1d1 antigen	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008036	abnormal NK T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587020
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10201995
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731798
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587020
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393151
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133426
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587020
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16675847
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21921158
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393151
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133426
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587020
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008698	abnormal interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587020
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22393151
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9133426
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20230601	MGI			
1552895	Cd1d1	CD1d1 antigen	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485631
1552895	Cd1d1	CD1d1 antigen	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21921158
1552895	Cd1d1	CD1d1 antigen	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20230601	MGI			
1552895	Cd1d1	CD1d1 antigen	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552895	Cd1d1	CD1d1 antigen	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902521
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736643
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14686897
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001349	excessive tearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736643
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612586
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736643
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736643
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:9718989
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0001994	increased blinking frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14686897
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736643
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141127	MGI			PMID:24270080
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12611922
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002913	abnormal PNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736643
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002918	abnormal paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612586
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0003483	decreased nerve fiber response threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:12611922
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141127	MGI			PMID:24270080
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14686897
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:9718989
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14686896
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12611922
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0005654	porphyria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0008282	enlarged hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17250763
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0008532	decreased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:9718989
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141127	MGI			PMID:24270080
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612586
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0013468	chromodacryorrhea		IAGP		N	RGD:5509061	20150205	MGI			PMID:8995755
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0014253	decreased paired-pulse ratio		IAGP		N	RGD:5509061	20230706	MGI			PMID:24270080
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0014625	abnormal ictal brain wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:9581771
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0031760	Mobitz I atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:20392939
1552897	Kcna1	potassium voltage-gated channel, shaker-related subfamily, member 1	gene	MP:0031761	Mobitz II atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:20392939
1552898	Crybb2	crystallin, beta B2	gene	MP:0000879	increased Purkinje cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385073
1552898	Crybb2	crystallin, beta B2	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18719080
1552898	Crybb2	crystallin, beta B2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11381063
1552898	Crybb2	crystallin, beta B2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385073
1552898	Crybb2	crystallin, beta B2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7363969
1552898	Crybb2	crystallin, beta B2	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:11381063
1552898	Crybb2	crystallin, beta B2	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385073
1552898	Crybb2	crystallin, beta B2	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:18719080
1552898	Crybb2	crystallin, beta B2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20200310	MGI			PMID:18385073
1552898	Crybb2	crystallin, beta B2	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20200310	MGI			PMID:18719080
1552898	Crybb2	crystallin, beta B2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11381063
1552898	Crybb2	crystallin, beta B2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18719080
1552898	Crybb2	crystallin, beta B2	gene	MP:0010251	subcapsular cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:7363969
1552898	Crybb2	crystallin, beta B2	gene	MP:0010254	nuclear cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:7363969
1552898	Crybb2	crystallin, beta B2	gene	MP:0010256	anterior cortical cataract		IAGP		N	RGD:5509061	20220428	MGI			PMID:18719080
1552898	Crybb2	crystallin, beta B2	gene	MP:0010257	posterior cortical cataract		IAGP		N	RGD:5509061	20220428	MGI			PMID:18719080
1552898	Crybb2	crystallin, beta B2	gene	MP:0010261	sutural cataract		IEA		N	RGD:5509061	20200310	MGI			
1552898	Crybb2	crystallin, beta B2	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:11381063
1552898	Crybb2	crystallin, beta B2	gene	MP:0010263	total cataract		IAGP		N	RGD:5509061	20220428	MGI			PMID:18719080
1552898	Crybb2	crystallin, beta B2	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:18385073
1552898	Crybb2	crystallin, beta B2	gene	MP:0031018	decreased granulosa cell proliferation		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220428	MGI			PMID:25245288
1552898	Crybb2	crystallin, beta B2	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:25245288
1552899	Cd180	CD180 antigen	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:10880523
1552899	Cd180	CD180 antigen	gene	MP:0001863	blood vessel inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0005265	abnormal blood urea nitrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552899	Cd180	CD180 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18492657
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20200310	MGI			
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20200310	MGI			
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552901	Tmem63b	transmembrane protein 63b	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20210429	MGI			PMID:32375046
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20241121	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20241121	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1552903	Or9g4	olfactory receptor family 9 subfamily G member 4	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20231207	MGI			
1552904	Rab21	RAB21, member RAS oncogene family	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1552904	Rab21	RAB21, member RAS oncogene family	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1552904	Rab21	RAB21, member RAS oncogene family	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1552904	Rab21	RAB21, member RAS oncogene family	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1552904	Rab21	RAB21, member RAS oncogene family	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0000520	absent kidney		IEA		N	RGD:5509061	20111116	MGI			
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0001565	abnormal circulating phosphate level		IEA		N	RGD:5509061	20230601	MGI			
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23840384
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0003313	abnormal locomotor activation		IEA		N	RGD:5509061	20220811	MGI			
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23840384
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23840384
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17724024
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23840384
1552905	Lcmt1	leucine carboxyl methyltransferase 1	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20241121	MGI			
1552909	Zbtb44	zinc finger and BTB domain containing 44	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468159
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468159
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244677
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000640	adrenal gland hypoplasia		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468159
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468159
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082260
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468159
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468159
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082260
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001705	abnormal proximal-distal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468159
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082260
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082260
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082260
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244677
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002345	abnormal lymph node primary follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244677
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468159
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002768	small adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082260
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003014	abnormal kidney medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003600	ectopic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003600	ectopic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082260
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082260
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22315423
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004204	absent stapes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004344	scapular bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005224	abnormal left-right axis symmetry of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005313	absent adrenal gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595835
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005492	exocrine pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0005651	abnormal gonad rudiment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14595835
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0006338	abnormal second pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0008023	abnormal styloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244677
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244677
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244677
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18462698
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0009173	absent pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912494
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0009902	abnormal lateral nasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0009903	abnormal medial nasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0010788	stomach hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0010788	stomach hypoplasia		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0010807	abnormal stomach position or orientation		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0010940	abnormal maxillary prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0010982	abnormal ureteric bud elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0010987	abnormal nephrogenic mesenchyme morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11468159
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17244677
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0011263	abnormal spleen mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22560297
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0011361	pelvic kidney		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591246
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0012491	larynx stenosis		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0013497	trachea occlusion		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20220512	MGI			PMID:31625560
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0014107	premature chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0014287	decreased adrenal gland zona fasciculata size		IAGP		N	RGD:5509061	20230907	MGI			PMID:17082260
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0021210	bilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0021211	unilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0030190	small snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0030297	outer ear hypoplasia		IAGP		N	RGD:5509061	20171221	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0030323	short styloid process		IAGP		N	RGD:5509061	20171214	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0030465	absent oval window		IAGP		N	RGD:5509061	20171221	MGI			PMID:11566859
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0031447	unilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:21982646
1552910	Pbx1	pre B cell leukemia homeobox 1	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:21982646
1552911	Hspb6	heat shock protein family B (small) member 6	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:38237739
1552911	Hspb6	heat shock protein family B (small) member 6	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20241121	MGI			PMID:38237739
1552911	Hspb6	heat shock protein family B (small) member 6	gene	MP:0031274	increased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20241121	MGI			PMID:38237739
1552911	Hspb6	heat shock protein family B (small) member 6	gene	MP:0031281	increased susceptibility to aneurysm induced morbidity/mortality		IAGP		N	RGD:5509061	20241121	MGI			PMID:38237739
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0003502	increased activity of thyroid gland		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0011019	abnormal adaptive thermogenesis		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552915	Adgra1	adhesion G protein-coupled receptor A1	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20230126	MGI			PMID:33824276
1552917	C6	complement component 6	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811844
1552917	C6	complement component 6	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959238
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20240523	MGI			
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15660130
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552918	Dnaja1	DnaJ heat shock protein family (Hsp40) member A1	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:15660130
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0009474	thick epidermis stratum spinosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0009599	thick epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0009715	thick epidermis stratum basale		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20170309	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20170309	MGI			PMID:27059959
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552921	Sgpp1	sphingosine-1-phosphate phosphatase 1	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637227
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12629211
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:21333627
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:21333627
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12629211
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12629211
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:12629211
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0004494	abnormal synaptic glutamate release		IAGP		N	RGD:5509061	20200310	MGI			PMID:16115873
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12629211
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0009434	paraparesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0009765	abnormal xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:16115873
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0009978	abnormal cerebellum white matter morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20200310	MGI			PMID:21333627
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0010734	abnormal paranode morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0010735	abnormal paranodal axoglial junction morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0012231	abnormal ganglioside level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0014114	abnormal cognition		IAGP		N	RGD:5509061	20200310	MGI			PMID:21333627
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15710896
1552922	St3gal5	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	gene	MP:0020194	abnormal glycosphingolipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16115873
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20231207	MGI			
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20231207	MGI			
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20231207	MGI			
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552926	Tars3	threonyl-tRNA synthetase 3	gene	MP:0013629	abnormal bone trabecular spacing		IAGP		N	RGD:5509061	20241128	MGI			PMID:37059185
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20210520	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20210826	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:22855807
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22855807
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20180201	MGI			PMID:24503275
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20180201	MGI			PMID:24503275
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20180201	MGI			PMID:24503275
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20150716	MGI			PMID:17236779
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150716	MGI			PMID:17236779
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20180201	MGI			PMID:24503275
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20180201	MGI			PMID:16020737
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20150716	MGI			PMID:17236779
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:16020737
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20150716	MGI			PMID:18930825
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16020737
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20221215	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0003214	neurofibrillary tangles		IAGP		N	RGD:5509061	20180201	MGI			PMID:16020737
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0003214	neurofibrillary tangles		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0003214	neurofibrillary tangles		IAGP		N	RGD:5509061	20180201	MGI			PMID:24503275
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20210520	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:24503275
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20210826	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16020737
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20240627	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:24503275
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:24503275
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:16020737
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12123606
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:17678857
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20150716	MGI			PMID:17236779
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20260402	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20150716	MGI			PMID:17236779
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0012508	forebrain atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:16020737
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0012508	forebrain atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:16291936
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:17236779
1552930	Fgf14	fibroblast growth factor 14	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:24503275
1552932	Npdc1	neural proliferation, differentiation and control 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15563841
1552934	Brix1	BRX1, biogenesis of ribosomes	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1552934	Brix1	BRX1, biogenesis of ribosomes	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1552934	Brix1	BRX1, biogenesis of ribosomes	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1552936	Pwwp3a	PWWP domain containing 3A, DNA repair factor	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20231207	MGI			
1552936	Pwwp3a	PWWP domain containing 3A, DNA repair factor	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1552936	Pwwp3a	PWWP domain containing 3A, DNA repair factor	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1552936	Pwwp3a	PWWP domain containing 3A, DNA repair factor	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1552936	Pwwp3a	PWWP domain containing 3A, DNA repair factor	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20211021	MGI			
1552936	Pwwp3a	PWWP domain containing 3A, DNA repair factor	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20240523	MGI			
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:14671308
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14671308
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14671308
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0003157	impaired muscle relaxation		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0004142	abnormal muscle tone		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0005620	abnormal muscle contractility		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0008802	abnormal intestinal smooth muscle morphology		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:14671308
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150305	MGI			PMID:24293317
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0013916	decreased intestine length		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0013958	decreased small intestine length		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0014575	increased intestinal transit time		IAGP		N	RGD:5509061	20260618	MGI			PMID:41379996
1552938	Mbnl1	muscleblind like splicing regulator 1	gene	MP:0031756	first degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:24293317
1552940	Tfap4	transcription factor AP4	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873191
1552940	Tfap4	transcription factor AP4	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210826	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0003049	abnormal lumbar vertebrae morphology		IEA		N	RGD:5509061	20210826	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0003050	abnormal sacral vertebrae morphology		IEA		N	RGD:5509061	20210826	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1552940	Tfap4	transcription factor AP4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21873191
1552940	Tfap4	transcription factor AP4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1552941	Myrip	myosin VIIA and Rab interacting protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191114	MGI			PMID:28673385
1552941	Myrip	myosin VIIA and Rab interacting protein	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20191114	MGI			PMID:28673385
1552941	Myrip	myosin VIIA and Rab interacting protein	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28673385
1552941	Myrip	myosin VIIA and Rab interacting protein	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28673385
1552941	Myrip	myosin VIIA and Rab interacting protein	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20191114	MGI			PMID:28673385
1552942	Rhob	ras homolog family member B	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597666
1552942	Rhob	ras homolog family member B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597666
1552942	Rhob	ras homolog family member B	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564874
1552942	Rhob	ras homolog family member B	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597666
1552942	Rhob	ras homolog family member B	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564874
1552942	Rhob	ras homolog family member B	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564874
1552942	Rhob	ras homolog family member B	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:19828736
1552942	Rhob	ras homolog family member B	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564874
1552942	Rhob	ras homolog family member B	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11564874
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0003572	abnormal uterus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0004514	dystocia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0008257	thin myometrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0013400	abnormal endometrial gland development		IAGP		N	RGD:5509061	20141218	MGI			PMID:21371262
1552944	Kpna1	karyopherin subunit alpha 1	gene	MP:0031137	vaginal hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:21371262
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333348
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0001565	abnormal circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333348
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333348
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0002901	increased urine phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333348
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333348
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21333348
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0004955	increased thymus weight		IEA		N	RGD:5509061	20211021	MGI			
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0009199	abnormal external male genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0009205	abnormal internal male genitalia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0011556	increased urine beta2-microglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19050760
1552947	Gprc6a	G protein-coupled receptor, family C, group 6, member A	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:21333348
1552948	Cetn1	centrin 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20191017	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220303	MGI			PMID:23641067
1552948	Cetn1	centrin 1	gene	MP:0031682	abnormal centriole morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:23641067
1552951	Impdh2	inosine monophosphate dehydrogenase 2	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1552951	Impdh2	inosine monophosphate dehydrogenase 2	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10953035
1552951	Impdh2	inosine monophosphate dehydrogenase 2	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1552951	Impdh2	inosine monophosphate dehydrogenase 2	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10953035
1552951	Impdh2	inosine monophosphate dehydrogenase 2	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1552951	Impdh2	inosine monophosphate dehydrogenase 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1552951	Impdh2	inosine monophosphate dehydrogenase 2	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944494
1552951	Impdh2	inosine monophosphate dehydrogenase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10953035
1552951	Impdh2	inosine monophosphate dehydrogenase 2	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10953035
1552955	Nrp1	neuropilin 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11891274
1552955	Nrp1	neuropilin 1	gene	MP:0000264	failure of vascular branching		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0000909	abnormal facial motor nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15545635
1552955	Nrp1	neuropilin 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15545635
1552955	Nrp1	neuropilin 1	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15814794
1552955	Nrp1	neuropilin 1	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15545635
1552955	Nrp1	neuropilin 1	gene	MP:0001072	abnormal vestibulocochlear nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15814794
1552955	Nrp1	neuropilin 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11891274
1552955	Nrp1	neuropilin 1	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:11891274
1552955	Nrp1	neuropilin 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20512151
1552955	Nrp1	neuropilin 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20512151
1552955	Nrp1	neuropilin 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:15550623
1552955	Nrp1	neuropilin 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:27844052
1552955	Nrp1	neuropilin 1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15814794
1552955	Nrp1	neuropilin 1	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11891274
1552955	Nrp1	neuropilin 1	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20200310	MGI			PMID:11891274
1552955	Nrp1	neuropilin 1	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0004159	double aortic arch		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1552955	Nrp1	neuropilin 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11891274
1552955	Nrp1	neuropilin 1	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21828096
1552955	Nrp1	neuropilin 1	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1552955	Nrp1	neuropilin 1	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0009945	abnormal accessory olfactory bulb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22745317
1552955	Nrp1	neuropilin 1	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:21852397
1552955	Nrp1	neuropilin 1	gene	MP:0010355	abnormal first pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0010356	abnormal second pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0010464	abnormal aortic arch and aortic arch branch attachment		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24401374
1552955	Nrp1	neuropilin 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12852851
1552955	Nrp1	neuropilin 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10518505
1552955	Nrp1	neuropilin 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11891274
1552955	Nrp1	neuropilin 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552955	Nrp1	neuropilin 1	gene	MP:0014554	delayed neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:15545635
1552955	Nrp1	neuropilin 1	gene	MP:0014592	decreased gonadotropin-releasing hormone neuron number		IAGP		N	RGD:5509061	20241212	MGI			PMID:21828096
1552955	Nrp1	neuropilin 1	gene	MP:0014748	abnormal sensory neuron axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:12852851
1552956	St8sia6	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1552956	St8sia6	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1552956	St8sia6	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210520	MGI			
1552956	St8sia6	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0001148	enlarged testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20200310	MGI			
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0001875	testis inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0003698	abnormal male reproductive system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200310	MGI			
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0004933	abnormal epididymis epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0004934	epididymis epithelium degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552958	Rnase10	ribonuclease, RNase A family, 10 (non-active)	gene	MP:0009198	abnormal male genitalia morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21084446
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:30842416
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191003	MGI			PMID:30842416
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20240523	MGI			
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20191003	MGI			PMID:30842416
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:30842416
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0008527	embryonic lethality at implantation		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0010158	abnormal intestine development		IAGP		N	RGD:5509061	20191003	MGI			PMID:30842416
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:30842416
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0011183	abnormal primitive endoderm morphology		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0011187	abnormal parietal endoderm morphology		IAGP		N	RGD:5509061	20241031	MGI			PMID:39194072
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210826	MGI			
1552959	Znhit1	zinc finger, HIT domain containing 1	gene	MP:0013485	increased Paneth cell number		IAGP		N	RGD:5509061	20191003	MGI			PMID:30842416
1552962	Cct2	chaperonin containing TCP1 subunit 2	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:38830954
1552962	Cct2	chaperonin containing TCP1 subunit 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:38830954
1552962	Cct2	chaperonin containing TCP1 subunit 2	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20241212	MGI			PMID:38830954
1552962	Cct2	chaperonin containing TCP1 subunit 2	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20241212	MGI			PMID:38830954
1552962	Cct2	chaperonin containing TCP1 subunit 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20241212	MGI			PMID:38830954
1552962	Cct2	chaperonin containing TCP1 subunit 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20241212	MGI			PMID:38830954
1552962	Cct2	chaperonin containing TCP1 subunit 2	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20241212	MGI			PMID:38830954
1552962	Cct2	chaperonin containing TCP1 subunit 2	gene	MP:0012034	abnormal a-wave shape		IAGP		N	RGD:5509061	20241212	MGI			PMID:38830954
1552962	Cct2	chaperonin containing TCP1 subunit 2	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:38830954
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20170413	MGI			PMID:27820699
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460747
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460747
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460747
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20170413	MGI			PMID:27820699
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20170413	MGI			PMID:27820699
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20170413	MGI			PMID:27820699
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20170413	MGI			PMID:27820699
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20170413	MGI			PMID:27820699
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460747
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460747
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460747
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460747
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460747
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0010760	abnormal macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23460747
1552963	Rpl13a	ribosomal protein L13A	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20170413	MGI			PMID:27820699
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20230601	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20230601	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230601	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20240523	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20250508	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20230601	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20231207	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1552964	Ubr7	ubiquitin protein ligase E3 component n-recognin 7 (putative)	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20230601	MGI			
1552965	Ppp1r2	protein phosphatase 1, regulatory inhibitor subunit 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20170831	MGI			PMID:26558779
1552965	Ppp1r2	protein phosphatase 1, regulatory inhibitor subunit 2	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20170831	MGI			PMID:26558779
1552965	Ppp1r2	protein phosphatase 1, regulatory inhibitor subunit 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170831	MGI			PMID:26558779
1552966	Ppp1r11	protein phosphatase 1, regulatory inhibitor subunit 11	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1552966	Ppp1r11	protein phosphatase 1, regulatory inhibitor subunit 11	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1552966	Ppp1r11	protein phosphatase 1, regulatory inhibitor subunit 11	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1552966	Ppp1r11	protein phosphatase 1, regulatory inhibitor subunit 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1552967	Calb2	calbindin 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220453
1552967	Calb2	calbindin 2	gene	MP:0001473	reduced long-term potentiation		IEA		N	RGD:5509061	20111116	MGI			
1552967	Calb2	calbindin 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1552967	Calb2	calbindin 2	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9294225
1552967	Calb2	calbindin 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10220453
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001007	abnormal sympathetic system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12160745
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12160745
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001011	abnormal superior cervical ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482239
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001011	abnormal superior cervical ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585795
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001011	abnormal superior cervical ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12160745
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001014	absent superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482239
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001015	small superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482239
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001015	small superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585795
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001015	small superior cervical ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12160745
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001025	abnormal sympathetic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12160745
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482239
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12160745
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15204970
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482239
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585795
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482239
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0009284	abnormal sympathetic neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482239
1552970	Gfra3	glial cell line derived neurotrophic factor family receptor alpha 3	gene	MP:0009561	superior cervical ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10482239
1552972	Nle1	notchless homolog 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20200310	MGI			PMID:16466971
1552972	Nle1	notchless homolog 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20200310	MGI			PMID:16611995
1552972	Nle1	notchless homolog 1	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16611995
1552972	Nle1	notchless homolog 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24062412
1552972	Nle1	notchless homolog 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16466971
1552972	Nle1	notchless homolog 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16611995
1552972	Nle1	notchless homolog 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23231322
1552972	Nle1	notchless homolog 1	gene	MP:0014242	abnormal ribosome biogenesis		IAGP		N	RGD:5509061	20230615	MGI			PMID:24062412
1552973	Hdhd2	haloacid dehalogenase-like hydrolase domain containing 2	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21937600
1552974	Tmem138	transmembrane protein 138	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1552974	Tmem138	transmembrane protein 138	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20201022	MGI			
1552974	Tmem138	transmembrane protein 138	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20211021	MGI			
1552974	Tmem138	transmembrane protein 138	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1552974	Tmem138	transmembrane protein 138	gene	MP:0009392	retina gliosis		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1552974	Tmem138	transmembrane protein 138	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552974	Tmem138	transmembrane protein 138	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20260312	MGI			PMID:35394880
1552975	Zfp579	zinc finger protein 579	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1552975	Zfp579	zinc finger protein 579	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1552975	Zfp579	zinc finger protein 579	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20220519	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20250508	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20220519	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210826	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220519	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20220519	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1552978	Cdh11	cadherin 11	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20231207	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20221215	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20221215	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545229
1552978	Cdh11	cadherin 11	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220811	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20221215	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0009682	abnormal anterior corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1552978	Cdh11	cadherin 11	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20220519	MGI			
1552978	Cdh11	cadherin 11	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20221215	MGI			
1552980	Ston1	stonin 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:26437238
1552980	Ston1	stonin 1	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20161103	MGI			PMID:26437238
1552980	Ston1	stonin 1	gene	MP:0011706	abnormal fibroblast migration		IAGP		N	RGD:5509061	20161103	MGI			PMID:26437238
1552980	Ston1	stonin 1	gene	MP:0014697	abnormal fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:26437238
1552982	Trub1	TruB pseudouridine (psi) synthase family member 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20240523	MGI			
1552982	Trub1	TruB pseudouridine (psi) synthase family member 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1552982	Trub1	TruB pseudouridine (psi) synthase family member 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20211021	MGI			
1552982	Trub1	TruB pseudouridine (psi) synthase family member 1	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1552982	Trub1	TruB pseudouridine (psi) synthase family member 1	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1552983	Il3ra	interleukin 3 receptor, alpha chain	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7889941
1552983	Il3ra	interleukin 3 receptor, alpha chain	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7727767
1552984	Or2b4	olfactory receptor family 2 subfamily B member 4	gene	MP:0001003	abnormal olfactory receptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923288
1552984	Or2b4	olfactory receptor family 2 subfamily B member 4	gene	MP:0001003	abnormal olfactory receptor morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:23688909
1552984	Or2b4	olfactory receptor family 2 subfamily B member 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923288
1552984	Or2b4	olfactory receptor family 2 subfamily B member 4	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19923288
1552984	Or2b4	olfactory receptor family 2 subfamily B member 4	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:23688909
1552984	Or2b4	olfactory receptor family 2 subfamily B member 4	gene	MP:0011677	abnormal olfactory sensory neuron physiology		IAGP		N	RGD:5509061	20150205	MGI			PMID:23688909
1552986	Tmem50b	transmembrane protein 50B	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20211021	MGI			
1552986	Tmem50b	transmembrane protein 50B	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1552986	Tmem50b	transmembrane protein 50B	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20211021	MGI			
1552991	Ilkap	integrin-linked kinase-associated serine/threonine phosphatase 2C	gene	MP:0003858	enhanced coordination		IEA		N	RGD:5509061	20200310	MGI			
1552991	Ilkap	integrin-linked kinase-associated serine/threonine phosphatase 2C	gene	MP:0003982	increased cholesterol level		IEA		N	RGD:5509061	20200310	MGI			
1552991	Ilkap	integrin-linked kinase-associated serine/threonine phosphatase 2C	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230119	MGI			
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20170126	MGI			PMID:17264314
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20170126	MGI			PMID:17264314
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0004755	abnormal loop of Henle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0004757	abnormal distal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0004899	absent temporal bone squamous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20170126	MGI			PMID:17264314
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20170126	MGI			PMID:17264314
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20170126	MGI			PMID:17264314
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20170126	MGI			PMID:17264314
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0008023	abnormal styloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12130536
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0011345	truncated loop of Henle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925600
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0015023	inverted cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:11859196
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0030111	absent temporomandibular joint		IAGP		N	RGD:5509061	20171207	MGI			PMID:18697905
1552994	Pou3f3	POU domain, class 3, transcription factor 3	gene	MP:0030394	abnormal incus short process morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:18697905
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201022	MGI			
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0012175	flat face		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20170223	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:27212239
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0031020	premature ovarian failure		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552997	Tmco1	transmembrane and coiled-coil domains 1	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220721	MGI			PMID:29467381
1552999	Ppp1r9a	protein phosphatase 1, regulatory subunit 9A	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600521
1552999	Ppp1r9a	protein phosphatase 1, regulatory subunit 9A	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600521
1552999	Ppp1r9a	protein phosphatase 1, regulatory subunit 9A	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600521
1552999	Ppp1r9a	protein phosphatase 1, regulatory subunit 9A	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600521
1552999	Ppp1r9a	protein phosphatase 1, regulatory subunit 9A	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:16600521
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:19419305
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:7840851
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000549	decreased limb number		IAGP		N	RGD:5509061	20200310	MGI			PMID:2884254
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000578	ulcerated autopod		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20200310	MGI			PMID:8118868
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:27670070
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:664185
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001189	absent skin pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:7840851
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20200310	MGI			PMID:16860389
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20200310	MGI			PMID:2884254
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19419305
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20200310	MGI			PMID:7840851
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:664185
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:2884254
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16860389
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:664185
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22724066
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:7840851
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001846	increased inflammatory response		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:664185
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20200310	MGI			PMID:6380298
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:664185
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:2884254
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:6380298
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002145	abnormal T cell differentiation		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002439	abnormal plasma cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:3551623
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1756226
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6334306
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002491	decreased IgD level		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:2884254
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:9586639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:7840851
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:11145649
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003201	extremity edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11145649
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003561	rheumatoid arthritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:7840851
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:664185
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:2884254
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:19419305
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20200310	MGI			PMID:11145649
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0004944	abnormal B cell negative selection		IAGP		N	RGD:5509061	20200310	MGI			PMID:9586639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0004978	decreased B-1 B cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:16860389
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11145649
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:3891855
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008126	increased dendritic cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008169	increased B-1b cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9586639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17600736
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008207	decreased B-2 B cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:3891855
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008215	decreased immature B cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19419305
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14987753
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:2884254
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:18806225
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20200310	MGI			PMID:19419305
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11745639
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:1184950
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0011130	absent tertiary ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:21435452
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200310	MGI			PMID:16505059
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:14987753
1553000	Ptpn6	protein tyrosine phosphatase, non-receptor type 6	gene	MP:0031234	increased circulating serum amyloid protein level		IAGP		N	RGD:5509061	20210225	MGI			PMID:21435452
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138930
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:6315811
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:6315811
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950794
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7202025
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303697
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530237
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692847
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692847
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000867	abnormal cerebellum anterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12528192
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000869	abnormal cerebellum posterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12528192
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12528192
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692847
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303697
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:11504598
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530237
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12528192
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6315811
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138930
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303697
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11530237
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056848
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303697
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:7202025
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950794
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22163015
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984826
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7202025
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303697
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001488	increased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001866	nasal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001921	reduced fertility		IEA		N	RGD:5509061	20111116	MGI			
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984826
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984826
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950794
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12528192
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790756
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314284
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056848
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303697
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7202025
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950794
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790756
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138930
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790756
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950794
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314284
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003191	abnormal cellular cholesterol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138930
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003191	abnormal cellular cholesterol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692847
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003191	abnormal cellular cholesterol metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303697
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17314284
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003947	abnormal cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6315811
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138930
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20191226	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6315811
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004781	abnormal surfactant composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0004894	uterus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138930
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6257302
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005499	abnormal olfactory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005544	cornea deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:22163015
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950794
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:15644330
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20190124	MGI			PMID:15644330
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008257	thin myometrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008258	thin endometrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692847
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008332	decreased lactotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008365	adenohypophysis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12692847
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008570	lipidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008570	lipidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6257302
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12528192
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24391715
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009081	thin uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20141003	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009287	decreased abdominal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009359	endometrium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009363	abnormal tertiary ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009587	abnormal plasma membrane sphingolipid content		IAGP		N	RGD:5509061	20141003	MGI			PMID:6315811
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009588	increased plasma membrane sphingolipid content		IAGP		N	RGD:5509061	20141003	MGI			PMID:6315811
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009589	sphingomyelinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009589	sphingomyelinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6315811
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009589	sphingomyelinosis		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009841	foam cell reticulosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0009841	foam cell reticulosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11984826
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21896731
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6315811
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20180201	MGI			PMID:11504598
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010052	increased grip strength		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010161	decreased brain cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11138930
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010161	decreased brain cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010162	increased brain cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303697
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010162	increased brain cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010162	increased brain cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010162	increased brain cholesterol level		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010162	increased brain cholesterol level		IAGP		N	RGD:5509061	20171207	MGI			PMID:21856732
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010162	increased brain cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:11138930
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010162	increased brain cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:20007718
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056848
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010762	abnormal microglial cell activation		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010813	abnormal alveolar lamellar body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010815	enlarged alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0010998	pulmonary alveolar proteinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20190124	MGI			PMID:15644330
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:15644330
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:15644330
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20190117	MGI			PMID:15465426
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9950794
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0012230	abnormal sphingolipid level		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20150709	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0012315	impaired learning		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:28379564
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0014270	decreased ovary secretion		IAGP		N	RGD:5509061	20230810	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0014329	abnormal Purkinje cell axon morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:11530237
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0014330	abnormal Purkinje cell focal axonal swelling		IAGP		N	RGD:5509061	20240118	MGI			PMID:12528192
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0014460	increased lipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:23843985
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0014460	increased lipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0014961	increased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22869680
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20240704	MGI			PMID:19056848
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20190926	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20240704	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:16850391
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:28167839
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:15105438
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0031560	decreased ganglioside level		IAGP		N	RGD:5509061	20240704	MGI			PMID:19056848
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0031561	increased ganglioside level		IAGP		N	RGD:5509061	20240704	MGI			PMID:19056848
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0031561	increased ganglioside level		IAGP		N	RGD:5509061	20240704	MGI			PMID:22048958
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0031561	increased ganglioside level		IAGP		N	RGD:5509061	20240704	MGI			PMID:26019327
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0031632	increased lung cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:18160655
1553002	Npc1	NPC intracellular cholesterol transporter 1	gene	MP:0031632	increased lung cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:23843985
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20170713	MGI			PMID:26344103
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0015000	decreased glucose oxidation		IAGP		N	RGD:5509061	20260611	MGI			PMID:30808746
1553003	Mpc1	mitochondrial pyruvate carrier 1	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:30808746
1553005	Trim31	tripartite motif-containing 31	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:27929086
1553005	Trim31	tripartite motif-containing 31	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27929086
1553005	Trim31	tripartite motif-containing 31	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:27929086
1553005	Trim31	tripartite motif-containing 31	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27929086
1553005	Trim31	tripartite motif-containing 31	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27929086
1553005	Trim31	tripartite motif-containing 31	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:27929086
1553005	Trim31	tripartite motif-containing 31	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1553005	Trim31	tripartite motif-containing 31	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:27929086
1553005	Trim31	tripartite motif-containing 31	gene	MP:0013022	increased Ly6C high monocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:27929086
1553007	Jph4	junctophilin 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:26929330
1553007	Jph4	junctophilin 4	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26929330
1553007	Jph4	junctophilin 4	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26929330
1553007	Jph4	junctophilin 4	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16809425
1553007	Jph4	junctophilin 4	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:16809425
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000467	abnormal esophagus morphology		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000524	decreased renal tubule number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000829	dilated fourth ventricle		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559594
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559594
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559594
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559594
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559594
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151112	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0002958	cerebral aqueductal stenosis		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559594
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23555292
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004548	dilated esophagus		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0006323	abnormal extraembryonic mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559594
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0008638	increased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0010152	abnormal brain ependyma morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20190516	MGI			PMID:28779153
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0011057	absent brain ependyma motile cilia		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559594
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0011202	abnormal ectoplacental cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559594
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0011518	abnormal cell chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11584271
1553011	Wasl	WASP like actin nucleation promoting factor	gene	MP:0012003	abnormal septum of telencephalon morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:24462670
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000033	absent scala media		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000035	abnormal membranous labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000035	abnormal membranous labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000041	absent endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000777	increased inferior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279136
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000847	abnormal metencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000848	abnormal pons morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279136
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000866	cerebellum vermis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19279136
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0001066	absent trigeminal nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0001092	abnormal trigeminal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847871
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003146	absent cochlear ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003163	absent posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003165	absent superior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003543	abnormal vascular endothelial cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003740	fusion of middle ear ossicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004096	abnormal midbrain-hindbrain boundary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004310	small otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004315	absent vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004330	abnormal vestibular saccular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004443	absent supraoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004568	fusion of glossopharyngeal and vagus nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20170921	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004923	absent common crus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0006287	inner ear cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0006289	otic capsule hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0006294	absent optic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0008023	abnormal styloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0009843	decreased neural crest cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9247335
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0012170	absent optic placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367504
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0012800	abnormal rhombomere 5 morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15829521
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0013906	absent embryonic telencephalon		IAGP		N	RGD:5509061	20150924	MGI			PMID:11731459
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0030124	middle ear ossicle hypoplasia		IAGP		N	RGD:5509061	20171005	MGI			PMID:15996652
1553014	Gbx2	gastrulation brain homeobox 2	gene	MP:0030322	styloid process hypoplasia		IAGP		N	RGD:5509061	20171109	MGI			PMID:15996652
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20220811	MGI			
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0008384	absent nasal capsule		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0010287	increased reproductive system tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20200310	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0010335	fused first pharyngeal arch		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0011189	small embryonic epiblast		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0012084	truncated foregut		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12447384
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0013906	absent embryonic telencephalon		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:21183657
1553015	Pcsk6	proprotein convertase subtilisin/kexin type 6	gene	MP:0030268	agnathia		IAGP		N	RGD:5509061	20200310	MGI			PMID:10809672
1553016	Pdlim2	PDZ and LIM domain 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15963787
1553016	Pdlim2	PDZ and LIM domain 2	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15963787
1553016	Pdlim2	PDZ and LIM domain 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15963787
1553017	Pno1	partner of NOB1 homolog	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029399
1553017	Pno1	partner of NOB1 homolog	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029399
1553018	Zdhhc20	zinc finger, DHHC domain containing 20	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20241121	MGI			
1553018	Zdhhc20	zinc finger, DHHC domain containing 20	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20201022	MGI			
1553018	Zdhhc20	zinc finger, DHHC domain containing 20	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20240905	MGI			PMID:38733589
1553018	Zdhhc20	zinc finger, DHHC domain containing 20	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201022	MGI			
1553018	Zdhhc20	zinc finger, DHHC domain containing 20	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20210520	MGI			
1553018	Zdhhc20	zinc finger, DHHC domain containing 20	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240905	MGI			PMID:38733589
1553018	Zdhhc20	zinc finger, DHHC domain containing 20	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:6736600
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0000048	abnormal stria vascularis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20200310	MGI			PMID:12647238
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:19436707
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20200310	MGI			
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:12647238
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0001923	reduced female fertility		IEA		N	RGD:5509061	20200310	MGI			
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20200310	MGI			
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19436707
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:6736600
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0002894	abnormal otolith morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15109702
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0002894	abnormal otolith morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20200310	MGI			PMID:6736600
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0003173	decreased lysosomal enzyme secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:1912584
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0003889	enhanced sensorimotor gating		IAGP		N	RGD:5509061	20200310	MGI			PMID:10586974
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0004721	abnormal platelet dense granule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1912584
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:1912584
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:10586974
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1912584
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0004813	absent linear vestibular evoked potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:15109702
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0004813	absent linear vestibular evoked potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:16235133
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:2778559
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:1912584
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20200310	MGI			PMID:1912584
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20200310	MGI			PMID:9585243
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20200310	MGI			PMID:10586974
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20200310	MGI			PMID:1912584
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0009617	decreased brain zinc level		IAGP		N	RGD:5509061	20240912	MGI			PMID:9697856
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0009617	decreased brain zinc level		IAGP		N	RGD:5509061	20251204	MGI			PMID:15537701
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20200310	MGI			PMID:20664521
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:4448900
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20200310	MGI			
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:20664521
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:2778559
1553020	Ap3d1	adaptor-related protein complex 3, delta 1 subunit	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20200310	MGI			PMID:1912584
1553023	Nutf2	nuclear transport factor 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1553023	Nutf2	nuclear transport factor 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1553023	Nutf2	nuclear transport factor 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1553023	Nutf2	nuclear transport factor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553026	Ssh3	slingshot protein phosphatase 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18442045
1553027	Spef2	sperm flagellar 2	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0001872	sinus inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0030316	enlarged neurocranium		IAGP		N	RGD:5509061	20171109	MGI			PMID:21715716
1553027	Spef2	sperm flagellar 2	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:21715716
1553028	Cnot10	CCR4-NOT transcription complex, subunit 10	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1553028	Cnot10	CCR4-NOT transcription complex, subunit 10	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1553028	Cnot10	CCR4-NOT transcription complex, subunit 10	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1553028	Cnot10	CCR4-NOT transcription complex, subunit 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20210826	MGI			
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20240404	MGI			PMID:36689511
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20240404	MGI			PMID:36689511
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1553029	Klk11	kallikrein related-peptidase 11	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20210128	MGI			
1553030	Thbd	thrombomodulin	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576763
1553030	Thbd	thrombomodulin	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7846065
1553030	Thbd	thrombomodulin	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576763
1553030	Thbd	thrombomodulin	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576763
1553030	Thbd	thrombomodulin	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:7846065
1553030	Thbd	thrombomodulin	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575060
1553030	Thbd	thrombomodulin	gene	MP:0001916	intracerebral hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7846065
1553030	Thbd	thrombomodulin	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7846065
1553030	Thbd	thrombomodulin	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573811
1553030	Thbd	thrombomodulin	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208873
1553030	Thbd	thrombomodulin	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208873
1553030	Thbd	thrombomodulin	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0003415	priapism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208873
1553030	Thbd	thrombomodulin	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0003913	increased heart right ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7846065
1553030	Thbd	thrombomodulin	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885846
1553030	Thbd	thrombomodulin	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573811
1553030	Thbd	thrombomodulin	gene	MP:0005243	hemothorax		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10233896
1553030	Thbd	thrombomodulin	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885846
1553030	Thbd	thrombomodulin	gene	MP:0005630	increased lung weight		IEA		N	RGD:5509061	20220811	MGI			
1553030	Thbd	thrombomodulin	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208873
1553030	Thbd	thrombomodulin	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573811
1553030	Thbd	thrombomodulin	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573811
1553030	Thbd	thrombomodulin	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573811
1553030	Thbd	thrombomodulin	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208873
1553030	Thbd	thrombomodulin	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208873
1553030	Thbd	thrombomodulin	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9576763
1553030	Thbd	thrombomodulin	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12208873
1553030	Thbd	thrombomodulin	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573811
1553030	Thbd	thrombomodulin	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573811
1553030	Thbd	thrombomodulin	gene	MP:0010211	abnormal acute phase protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8575060
1553030	Thbd	thrombomodulin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7846065
1553030	Thbd	thrombomodulin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553030	Thbd	thrombomodulin	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885846
1553030	Thbd	thrombomodulin	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885846
1553030	Thbd	thrombomodulin	gene	MP:0011514	skin hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0012501	abnormal pericardial cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1553030	Thbd	thrombomodulin	gene	MP:0014502	decreased circulating protein level		IAGP		N	RGD:5509061	20260409	MGI			PMID:21885846
1553030	Thbd	thrombomodulin	gene	MP:0020407	abnormal placental thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0030975	placenta hemorrhage		IAGP		N	RGD:5509061	20191010	MGI			PMID:12579195
1553030	Thbd	thrombomodulin	gene	MP:0031083	increased circulating D-dimer level		IAGP		N	RGD:5509061	20200709	MGI			PMID:11518727
1553030	Thbd	thrombomodulin	gene	MP:0031083	increased circulating D-dimer level		IAGP		N	RGD:5509061	20200709	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0031121	increased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:11557684
1553030	Thbd	thrombomodulin	gene	MP:0031167	abnormal lung thrombosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:9576763
1553035	Nrxn3	neurexin III	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23827676
1553035	Nrxn3	neurexin III	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983056
1553035	Nrxn3	neurexin III	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111215	MGI			
1553035	Nrxn3	neurexin III	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:14983056
1553035	Nrxn3	neurexin III	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0002915	abnormal synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0003459	increased fear-related response		IAGP		N	RGD:5509061	20260813	MGI			PMID:29681532
1553035	Nrxn3	neurexin III	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23827676
1553035	Nrxn3	neurexin III	gene	MP:0004807	abnormal paired-pulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0005386	behavior/neurological phenotype		IAGP		N	RGD:5509061	20260813	MGI			PMID:29681532
1553035	Nrxn3	neurexin III	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23827676
1553035	Nrxn3	neurexin III	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:12827191
1553035	Nrxn3	neurexin III	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:23827676
1553036	Acy3	aminoacylase 3	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1553036	Acy3	aminoacylase 3	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20220811	MGI			
1553036	Acy3	aminoacylase 3	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1553036	Acy3	aminoacylase 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1553036	Acy3	aminoacylase 3	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220811	MGI			
1553039	Chst15	carbohydrate sulfotransferase 15	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439988
1553039	Chst15	carbohydrate sulfotransferase 15	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20439988
1553041	Rbm25	RNA binding motif protein 25	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20201231	MGI			
1553041	Rbm25	RNA binding motif protein 25	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201231	MGI			
1553041	Rbm25	RNA binding motif protein 25	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1553041	Rbm25	RNA binding motif protein 25	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553041	Rbm25	RNA binding motif protein 25	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1553045	Numa1	nuclear mitotic apparatus protein 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19255246
1553045	Numa1	nuclear mitotic apparatus protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19255246
1553045	Numa1	nuclear mitotic apparatus protein 1	gene	MP:0011705	absent fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19255246
1553051	Clec4f	C-type lectin domain family 4, member f	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23762286
1553051	Clec4f	C-type lectin domain family 4, member f	gene	MP:0011072	abnormal macrophage cytokine production		IAGP		N	RGD:5509061	20200310	MGI			PMID:23762286
1553053	Phf21b	PHD finger protein 21B	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20220929	MGI			PMID:35866480
1553053	Phf21b	PHD finger protein 21B	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20220929	MGI			PMID:35866480
1553053	Phf21b	PHD finger protein 21B	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:35866480
1553053	Phf21b	PHD finger protein 21B	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20220929	MGI			PMID:35866480
1553053	Phf21b	PHD finger protein 21B	gene	MP:0012066	decreased astrocyte number		IAGP		N	RGD:5509061	20220929	MGI			PMID:35866480
1553053	Phf21b	PHD finger protein 21B	gene	MP:0020514	abnormal dendritic thin spine morphology		IAGP		N	RGD:5509061	20220929	MGI			PMID:35866480
1553053	Phf21b	PHD finger protein 21B	gene	MP:0021112	impaired social recognition		IAGP		N	RGD:5509061	20220929	MGI			PMID:35866480
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20250515	MGI			PMID:40154727
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20250515	MGI			PMID:40154727
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22110650
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20170223	MGI			PMID:27143553
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20170223	MGI			PMID:27143553
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20170223	MGI			PMID:27143553
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0005239	abnormal Bruch membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20170223	MGI			PMID:27143553
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0008448	abnormal retina cone cell inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0008455	abnormal retina rod cell inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20170223	MGI			PMID:27143553
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20170223	MGI			PMID:27143553
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20240404	MGI			PMID:21349921
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20170223	MGI			PMID:27143553
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0030973	impaired gluconeogenesis		IAGP		N	RGD:5509061	20200102	MGI			PMID:27143553
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20250515	MGI			PMID:40154727
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:27143553
1553055	C1qtnf5	C1q and tumor necrosis factor related protein 5	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:21349921
1553057	Slc25a26	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14504232
1553057	Slc25a26	solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14504232
1553058	Slc17a2	solute carrier family 17 (sodium phosphate), member 2	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210128	MGI			
1553058	Slc17a2	solute carrier family 17 (sodium phosphate), member 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1553059	Nanog	Nanog homeobox	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787504
1553059	Nanog	Nanog homeobox	gene	MP:0002583	absent extraembryonic ectoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787504
1553059	Nanog	Nanog homeobox	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20435031
1553059	Nanog	Nanog homeobox	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20435031
1553059	Nanog	Nanog homeobox	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787504
1553059	Nanog	Nanog homeobox	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20435031
1553059	Nanog	Nanog homeobox	gene	MP:0011184	absent embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:12787504
1553059	Nanog	Nanog homeobox	gene	MP:0011185	absent primitive endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20435031
1553060	Gphb5	glycoprotein hormone beta 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699348
1553060	Gphb5	glycoprotein hormone beta 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16210345
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0004089	dilated sarcoplasmic reticulum		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0009777	abnormal behavioral response to anesthetic		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0010052	increased grip strength		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0010394	decreased QRS amplitude		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0010520	sinoatrial block		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0011634	abnormal mitochondrial inner membrane morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0014390	decreased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:25506927
1553062	Mto1	mitochondrial tRNA translation optimization 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25506927
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30485550
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:30485550
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20230119	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:30485550
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210128	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20210128	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20230119	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:30485550
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20220519	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:30485550
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1553063	Nsun5	NOL1/NOP2/Sun domain family, member 5	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1553064	Fasl	Fas ligand	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15980239
1553064	Fasl	Fas ligand	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16118350
1553064	Fasl	Fas ligand	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:21479271
1553064	Fasl	Fas ligand	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:21479271
1553064	Fasl	Fas ligand	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:23577189
1553064	Fasl	Fas ligand	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:9736651
1553064	Fasl	Fas ligand	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17803905
1553064	Fasl	Fas ligand	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20053716
1553064	Fasl	Fas ligand	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16118350
1553064	Fasl	Fas ligand	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0001800	abnormal humoral immune response		IEA		N	RGD:5509061	20200310	MGI			
1553064	Fasl	Fas ligand	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20200310	MGI			
1553064	Fasl	Fas ligand	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9736651
1553064	Fasl	Fas ligand	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15980239
1553064	Fasl	Fas ligand	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23577189
1553064	Fasl	Fas ligand	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16118350
1553064	Fasl	Fas ligand	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0001863	blood vessel inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:3009614
1553064	Fasl	Fas ligand	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:3856256
1553064	Fasl	Fas ligand	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:15980239
1553064	Fasl	Fas ligand	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:3009614
1553064	Fasl	Fas ligand	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20971954
1553064	Fasl	Fas ligand	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16118350
1553064	Fasl	Fas ligand	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14764677
1553064	Fasl	Fas ligand	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11567045
1553064	Fasl	Fas ligand	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23577189
1553064	Fasl	Fas ligand	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21479271
1553064	Fasl	Fas ligand	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23577189
1553064	Fasl	Fas ligand	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20200310	MGI			
1553064	Fasl	Fas ligand	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:7512035
1553064	Fasl	Fas ligand	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:3009614
1553064	Fasl	Fas ligand	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20971954
1553064	Fasl	Fas ligand	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:12045257
1553064	Fasl	Fas ligand	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23577189
1553064	Fasl	Fas ligand	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23577189
1553064	Fasl	Fas ligand	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:23577189
1553064	Fasl	Fas ligand	gene	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20971954
1553064	Fasl	Fas ligand	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15980239
1553064	Fasl	Fas ligand	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15096538
1553064	Fasl	Fas ligand	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9736651
1553064	Fasl	Fas ligand	gene	MP:0006303	abnormal retina nerve fiber layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21479271
1553064	Fasl	Fas ligand	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21479271
1553064	Fasl	Fas ligand	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:3009614
1553064	Fasl	Fas ligand	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21479271
1553064	Fasl	Fas ligand	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:21479271
1553064	Fasl	Fas ligand	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20971954
1553064	Fasl	Fas ligand	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20971954
1553064	Fasl	Fas ligand	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20220714	MGI			PMID:18818293
1553064	Fasl	Fas ligand	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20200310	MGI			PMID:6693832
1553064	Fasl	Fas ligand	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:3009614
1553064	Fasl	Fas ligand	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0008891	decreased hepatocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16118350
1553064	Fasl	Fas ligand	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9834083
1553064	Fasl	Fas ligand	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0011506	glomerular crescent		IAGP		N	RGD:5509061	20200310	MGI			PMID:19794494
1553064	Fasl	Fas ligand	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:16935260
1553064	Fasl	Fas ligand	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20200310	MGI			
1553064	Fasl	Fas ligand	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:9736651
1553064	Fasl	Fas ligand	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21479271
1553064	Fasl	Fas ligand	gene	MP:0030603	increased sperm number		IAGP		N	RGD:5509061	20220714	MGI			PMID:18818293
1553065	Armc7	armadillo repeat containing 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553065	Armc7	armadillo repeat containing 7	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553065	Armc7	armadillo repeat containing 7	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1553066	Msto1	misato 1, mitochondrial distribution and morphology regulator	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220519	MGI			
1553066	Msto1	misato 1, mitochondrial distribution and morphology regulator	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1553066	Msto1	misato 1, mitochondrial distribution and morphology regulator	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20200514	MGI			
1553066	Msto1	misato 1, mitochondrial distribution and morphology regulator	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20200514	MGI			
1553066	Msto1	misato 1, mitochondrial distribution and morphology regulator	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220519	MGI			
1553066	Msto1	misato 1, mitochondrial distribution and morphology regulator	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20220519	MGI			
1553066	Msto1	misato 1, mitochondrial distribution and morphology regulator	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200514	MGI			
1553066	Msto1	misato 1, mitochondrial distribution and morphology regulator	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20200310	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20200310	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20200310	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20221215	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20200310	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20221215	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20200310	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20200310	MGI			
1553072	Mars2	methionine-tRNA synthetase 2 (mitochondrial)	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1553073	Krt17	keratin 17	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1553073	Krt17	keratin 17	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601842
1553073	Krt17	keratin 17	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601842
1553073	Krt17	keratin 17	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1553073	Krt17	keratin 17	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1553073	Krt17	keratin 17	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1553073	Krt17	keratin 17	gene	MP:0003413	hair follicle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601842
1553073	Krt17	keratin 17	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0003812	abnormal hair medulla		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0005072	abnormal hair follicle melanin granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20201022	MGI			
1553073	Krt17	keratin 17	gene	MP:0010686	abnormal hair follicle matrix region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601842
1553073	Krt17	keratin 17	gene	MP:0011195	increased hair follicle apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050118
1553073	Krt17	keratin 17	gene	MP:0014693	abnormal cell nucleus size		IAGP		N	RGD:5509061	20250710	MGI			PMID:33008845
1553074	Chpt1	choline phosphotransferase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553075	Nudt5	nudix hydrolase 5	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1553075	Nudt5	nudix hydrolase 5	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1553075	Nudt5	nudix hydrolase 5	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1553075	Nudt5	nudix hydrolase 5	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1553077	Nucleolin	nucleolin multifunctional protein	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20220113	MGI			PMID:34515347
1553077	Nucleolin	nucleolin multifunctional protein	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20220113	MGI			PMID:34515347
1553078	Chmp3	charged multivesicular body protein 3	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20201231	MGI			
1553078	Chmp3	charged multivesicular body protein 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20241121	MGI			
1553078	Chmp3	charged multivesicular body protein 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1553078	Chmp3	charged multivesicular body protein 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553078	Chmp3	charged multivesicular body protein 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553079	Crcp	calcitonin gene-related peptide-receptor component protein	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20240523	MGI			
1553079	Crcp	calcitonin gene-related peptide-receptor component protein	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1553079	Crcp	calcitonin gene-related peptide-receptor component protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553079	Crcp	calcitonin gene-related peptide-receptor component protein	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553080	Dctn2	dynactin 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28900001
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20201022	MGI			
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20230907	MGI			PMID:33603070
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20230907	MGI			PMID:33603070
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20230907	MGI			PMID:33603070
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28900001
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20230907	MGI			PMID:33603070
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20230907	MGI			PMID:33603070
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20230907	MGI			PMID:33603070
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200310	MGI			PMID:28900001
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20230907	MGI			PMID:33603070
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200310	MGI			PMID:28900001
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20230907	MGI			PMID:33603070
1553081	Samd7	sterile alpha motif domain containing 7	gene	MP:0012150	increased b-wave implicit time		IAGP		N	RGD:5509061	20230907	MGI			PMID:33603070
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20200514	MGI			
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553084	Sipa1	signal-induced proliferation associated gene 1	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12892713
1553085	Serinc1	serine incorporator 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20141003	MGI			
1553085	Serinc1	serine incorporator 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1553085	Serinc1	serine incorporator 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1553087	Gdpd3	glycerophosphodiester phosphodiesterase domain containing 3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1553087	Gdpd3	glycerophosphodiester phosphodiesterase domain containing 3	gene	MP:0012443	increased corpus callosum size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1553087	Gdpd3	glycerophosphodiester phosphodiesterase domain containing 3	gene	MP:0012450	decreased primary motor cortex size		IAGP		N	RGD:5509061	20250612	MGI			PMID:37968726
1553087	Gdpd3	glycerophosphodiester phosphodiesterase domain containing 3	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210722	MGI			PMID:30224518
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15241416
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20200310	MGI			PMID:15671285
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15671285
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15671285
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001862	interstitial pneumonia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0002433	abnormal T-helper 1 cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15241416
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15241416
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0004481	abnormal conjunctival epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15671285
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0006167	eyelid edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0006167	eyelid edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0008556	abnormal tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15241416
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15241416
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:15241416
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15491998
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0012164	abnormal conjunctiva goblet cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15241416
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0013452	increased lacrimal gland apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0013459	perioral dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0013460	periocular dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0013464	decreased conjunctiva goblet cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15671285
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0013464	decreased conjunctiva goblet cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18441309
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0013478	corneal limbitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15671285
1553089	Nfkbiz	nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta	gene	MP:0020220	decreased tear production		IAGP		N	RGD:5509061	20200310	MGI			PMID:23453632
1553090	Rab8b	RAB8B, member RAS oncogene family	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24213529
1553090	Rab8b	RAB8B, member RAS oncogene family	gene	MP:0008109	abnormal small intestinal microvillus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24213529
1553090	Rab8b	RAB8B, member RAS oncogene family	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24213529
1553094	Klk12	kallikrein related-peptidase 12	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1553094	Klk12	kallikrein related-peptidase 12	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20201231	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20201022	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20201022	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20201022	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20201022	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20200514	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20200514	MGI			
1553096	Zfand6	zinc finger, AN1-type domain 6	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20221215	MGI			
1553097	Fbxo45	F-box protein 45	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0001512	trunk curl		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0008129	absent brain internal capsule		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0008503	abnormal spinal cord grey matter morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553097	Fbxo45	F-box protein 45	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19398581
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20111116	MGI			
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20865721
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088125
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20865721
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0002084	abnormal developmental patterning		IEA		N	RGD:5509061	20111116	MGI			
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088125
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:36073547
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0005032	abnormal ectoplacental cone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0005241	abnormal retina ganglion layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088125
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088125
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088125
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0008106	decreased amacrine cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088125
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20865721
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20230601	MGI			PMID:36073547
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15668733
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20865721
1553098	Atrx	ATRX, chromatin remodeler	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16628246
1553101	Gprasp1	G protein-coupled receptor associated sorting protein 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19712096
1553101	Gprasp1	G protein-coupled receptor associated sorting protein 1	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:19712096
1553101	Gprasp1	G protein-coupled receptor associated sorting protein 1	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:20543951
1553104	Yipf1	Yip1 domain family, member 1	gene	MP:0001391	abnormal tail movements		IEA		N	RGD:5509061	20200310	MGI			
1553104	Yipf1	Yip1 domain family, member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:24652767
1553107	Nox3	NADPH oxidase 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434016
1553107	Nox3	NADPH oxidase 3	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1553107	Nox3	NADPH oxidase 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:9755211
1553107	Nox3	NADPH oxidase 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20111116	MGI			
1553107	Nox3	NADPH oxidase 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15014044
1553107	Nox3	NADPH oxidase 3	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
1553107	Nox3	NADPH oxidase 3	gene	MP:0001443	poor grooming		IEA		N	RGD:5509061	20111116	MGI			
1553107	Nox3	NADPH oxidase 3	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434016
1553107	Nox3	NADPH oxidase 3	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:15014044
1553107	Nox3	NADPH oxidase 3	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:9755211
1553107	Nox3	NADPH oxidase 3	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15014044
1553107	Nox3	NADPH oxidase 3	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491954
1553107	Nox3	NADPH oxidase 3	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491954
1553107	Nox3	NADPH oxidase 3	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:15014044
1553107	Nox3	NADPH oxidase 3	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:21161235
1553107	Nox3	NADPH oxidase 3	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:9755211
1553107	Nox3	NADPH oxidase 3	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15014044
1553107	Nox3	NADPH oxidase 3	gene	MP:0004813	absent linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491954
1553107	Nox3	NADPH oxidase 3	gene	MP:0004845	absent vestibuloocular reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12711080
1553107	Nox3	NADPH oxidase 3	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491954
1553107	Nox3	NADPH oxidase 3	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:10835400
1553107	Nox3	NADPH oxidase 3	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:15014044
1553107	Nox3	NADPH oxidase 3	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:21161235
1553107	Nox3	NADPH oxidase 3	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:9755211
1553107	Nox3	NADPH oxidase 3	gene	MP:0005424	jerky movement		IEA		N	RGD:5509061	20111116	MGI			
1553107	Nox3	NADPH oxidase 3	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434016
1553107	Nox3	NADPH oxidase 3	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434016
1553107	Nox3	NADPH oxidase 3	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20171012	MGI			PMID:12434016
1553107	Nox3	NADPH oxidase 3	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:12434016
1553108	Ldhal6b	lactate dehydrogenase A-like 6B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210826	MGI			
1553109	Ehd3	EH-domain containing 3	gene	MP:0000530	abnormal kidney vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011294	renal glomerulus hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011369	increased renal glomerulus apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011430	mesangiolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011455	absent glomerular endothelium fenestra		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553109	Ehd3	EH-domain containing 3	gene	MP:0011512	mesangial cell interposition		IAGP		N	RGD:5509061	20141003	MGI			PMID:21408024
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20200310	MGI			
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0001125	abnormal oocyte morphology		IEA		N	RGD:5509061	20111116	MGI			
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20200310	MGI			
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220519	MGI			
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0001932	abnormal spermiogenesis		IEA		N	RGD:5509061	20111116	MGI			
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20200310	MGI			
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20200310	MGI			
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0002687	oligozoospermia		IEA		N	RGD:5509061	20111116	MGI			
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220519	MGI			
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553111	Brwd1	bromodomain and WD repeat domain containing 1	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18353305
1553115	Ifnk	interferon kappa	gene	MP:0000452	abnormal mouth morphology		IEA		N	RGD:5509061	20181227	MGI			
1553115	Ifnk	interferon kappa	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20220407	MGI			PMID:34364883
1553115	Ifnk	interferon kappa	gene	MP:0012573	decreased susceptibility to chemically induced skin inflammation		IAGP		N	RGD:5509061	20220407	MGI			PMID:34364883
1553116	Lrrc41	leucine rich repeat containing 41	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1553116	Lrrc41	leucine rich repeat containing 41	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1553116	Lrrc41	leucine rich repeat containing 41	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1553116	Lrrc41	leucine rich repeat containing 41	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1553116	Lrrc41	leucine rich repeat containing 41	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1553116	Lrrc41	leucine rich repeat containing 41	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1553116	Lrrc41	leucine rich repeat containing 41	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1553116	Lrrc41	leucine rich repeat containing 41	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1553116	Lrrc41	leucine rich repeat containing 41	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1553117	Krt5	keratin 5	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11408584
1553117	Krt5	keratin 5	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11408584
1553117	Krt5	keratin 5	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11408584
1553117	Krt5	keratin 5	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11408584
1553117	Krt5	keratin 5	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11408584
1553117	Krt5	keratin 5	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11408584
1553117	Krt5	keratin 5	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1553117	Krt5	keratin 5	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11408584
1553117	Krt5	keratin 5	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:11408584
1553117	Krt5	keratin 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11408584
1553117	Krt5	keratin 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1553117	Krt5	keratin 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553119	Slc9c1	solute carrier family 9, subfamily C (Na+-transporting carboxylic acid decarboxylase), member 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:14634667
1553119	Slc9c1	solute carrier family 9, subfamily C (Na+-transporting carboxylic acid decarboxylase), member 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14634667
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232663
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872314
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232663
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232663
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232663
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872314
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232663
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872314
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0005345	abnormal circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872314
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22232663
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872314
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897241
1553120	Pmch	pro-melanin-concentrating hormone	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:9872314
1553121	Frmd4a	FERM domain containing 4A	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1553121	Frmd4a	FERM domain containing 4A	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220519	MGI			
1553121	Frmd4a	FERM domain containing 4A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1553125	Toe1	target of EGR1, member 1 (nuclear)	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201231	MGI			
1553125	Toe1	target of EGR1, member 1 (nuclear)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20191114	MGI			PMID:28092684
1553125	Toe1	target of EGR1, member 1 (nuclear)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553125	Toe1	target of EGR1, member 1 (nuclear)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20220811	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20241003	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220811	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241003	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241003	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20241003	MGI			
1553126	Nifk	nucleolar protein interacting with the FHA domain of MKI67	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20211104	MGI			PMID:26240281
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20150702	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20211104	MGI			PMID:26240281
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0004264	abnormal extraembryonic tissue physiology		IAGP		N	RGD:5509061	20211104	MGI			PMID:26240281
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24469832
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20211104	MGI			PMID:26240281
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20211104	MGI			PMID:26240281
1553129	Fbxw11	F-box and WD-40 domain protein 11	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:24469832
1553130	Atf5	activating transcription factor 5	gene	MP:0001003	abnormal olfactory receptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24120133
1553130	Atf5	activating transcription factor 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090999
1553130	Atf5	activating transcription factor 5	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090999
1553130	Atf5	activating transcription factor 5	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24120133
1553130	Atf5	activating transcription factor 5	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:24120133
1553130	Atf5	activating transcription factor 5	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090999
1553130	Atf5	activating transcription factor 5	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090999
1553130	Atf5	activating transcription factor 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090999
1553130	Atf5	activating transcription factor 5	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090999
1553131	Hyal4	hyaluronoglucosaminidase 4	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201231	MGI			
1553131	Hyal4	hyaluronoglucosaminidase 4	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20220811	MGI			
1553135	Slc12a8	solute carrier family 12 (potassium/chloride transporters), member 8	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1553135	Slc12a8	solute carrier family 12 (potassium/chloride transporters), member 8	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20191128	MGI			PMID:31131364
1553135	Slc12a8	solute carrier family 12 (potassium/chloride transporters), member 8	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20191128	MGI			PMID:31131364
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0000256	echinocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0008809	increased spleen iron level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0010035	increased erythrocyte clearance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553136	Nmnat3	nicotinamide nucleotide adenylyltransferase 3	gene	MP:0010177	acanthocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739386
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17212650
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22114263
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20200310	MGI			PMID:17212650
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20200310	MGI			PMID:17212650
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:25740289
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:17212650
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:22114263
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:22114263
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:22114263
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17212650
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25740289
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22114263
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0011016	increased core body temperature		IAGP		N	RGD:5509061	20200310	MGI			PMID:22114263
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0012342	high preference for an addictive substance		IAGP		N	RGD:5509061	20220317	MGI			PMID:34512422
1553140	Taar1	trace amine-associated receptor 1	gene	MP:0012733	abnormal behavioral response to methamphetamine		IAGP		N	RGD:5509061	20220317	MGI			PMID:34512422
1553142	Fam13b	family with sequence similarity 13, member B	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1553142	Fam13b	family with sequence similarity 13, member B	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20241212	MGI			PMID:38094680
1553142	Fam13b	family with sequence similarity 13, member B	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20241212	MGI			PMID:38094680
1553142	Fam13b	family with sequence similarity 13, member B	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20241212	MGI			PMID:38094680
1553142	Fam13b	family with sequence similarity 13, member B	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20241212	MGI			PMID:38094680
1553142	Fam13b	family with sequence similarity 13, member B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553142	Fam13b	family with sequence similarity 13, member B	gene	MP:0031717	prolonged corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:38094680
1553143	Pnpla5	patatin-like phospholipase domain containing 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1553143	Pnpla5	patatin-like phospholipase domain containing 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1553146	Wdr77	WD repeat domain 77	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17032745
1553146	Wdr77	WD repeat domain 77	gene	MP:0000666	decreased prostate gland duct number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17032745
1553146	Wdr77	WD repeat domain 77	gene	MP:0001167	prostate gland epithelial hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17032745
1553146	Wdr77	WD repeat domain 77	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0002774	small prostate gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0003607	abnormal prostate gland physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0009380	abnormal prostate gland ventral lobe morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0009381	abnormal prostate gland dorsolateral lobe morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0009734	abnormal prostate gland duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0009735	abnormal prostate gland development		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0009736	abnormal prostate gland branching morphogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20519372
1553146	Wdr77	WD repeat domain 77	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17032745
1553147	Hs1bp3	HCLS1 binding protein 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1553147	Hs1bp3	HCLS1 binding protein 3	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20250508	MGI			
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8064243
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:9647223
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0002144	abnormal B cell differentiation		IEA		N	RGD:5509061	20200310	MGI			
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0002493	increased IgG level		IEA		N	RGD:5509061	20200310	MGI			
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:8064243
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:9647223
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0004918	abnormal negative T cell selection		IAGP		N	RGD:5509061	20200310	MGI			PMID:7889415
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20200310	MGI			PMID:7889415
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8064243
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:9647223
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7889415
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:7889415
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:9647223
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:7889415
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17082573
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17082573
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:7889415
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8064243
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:9647223
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:8064243
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:7889415
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20200310	MGI			
1553149	Cd8b1	CD8 subunit beta 1	gene	MP:0020155	enhanced humoral immune response		IEA		N	RGD:5509061	20200310	MGI			
1553151	Or2y1g	olfactory receptor family 2 subfamily Y member 1G	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20190905	MGI			PMID:27739476
1553151	Or2y1g	olfactory receptor family 2 subfamily Y member 1G	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20190905	MGI			PMID:27739476
1553154	Gpaa1	GPI anchor attachment protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1553154	Gpaa1	GPI anchor attachment protein 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20201231	MGI			
1553154	Gpaa1	GPI anchor attachment protein 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1553154	Gpaa1	GPI anchor attachment protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553154	Gpaa1	GPI anchor attachment protein 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200310	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0000947	convulsive seizures		IEA		N	RGD:5509061	20260402	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14978268
1553155	Foxo3	forkhead box O3	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26061565
1553155	Foxo3	forkhead box O3	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20200310	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20200310	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25264246
1553155	Foxo3	forkhead box O3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0001749	suppressed circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26061565
1553155	Foxo3	forkhead box O3	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371339
1553155	Foxo3	forkhead box O3	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:26061565
1553155	Foxo3	forkhead box O3	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25264246
1553155	Foxo3	forkhead box O3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371339
1553155	Foxo3	forkhead box O3	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371339
1553155	Foxo3	forkhead box O3	gene	MP:0002681	increased corpora lutea number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:14978268
1553155	Foxo3	forkhead box O3	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:25264246
1553155	Foxo3	forkhead box O3	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26061565
1553155	Foxo3	forkhead box O3	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371339
1553155	Foxo3	forkhead box O3	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:25264246
1553155	Foxo3	forkhead box O3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20210520	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0003505	increased prolactinoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18601916
1553155	Foxo3	forkhead box O3	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25264246
1553155	Foxo3	forkhead box O3	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371339
1553155	Foxo3	forkhead box O3	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371339
1553155	Foxo3	forkhead box O3	gene	MP:0004832	enlarged ovary		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0004832	enlarged ovary		IAGP		N	RGD:5509061	20200310	MGI			PMID:18601916
1553155	Foxo3	forkhead box O3	gene	MP:0004832	enlarged ovary		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0005068	abnormal NK cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17618288
1553155	Foxo3	forkhead box O3	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26061565
1553155	Foxo3	forkhead box O3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25264246
1553155	Foxo3	forkhead box O3	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:26061565
1553155	Foxo3	forkhead box O3	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371339
1553155	Foxo3	forkhead box O3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25264246
1553155	Foxo3	forkhead box O3	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17618288
1553155	Foxo3	forkhead box O3	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17618288
1553155	Foxo3	forkhead box O3	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:26061565
1553155	Foxo3	forkhead box O3	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:17618288
1553155	Foxo3	forkhead box O3	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:14978268
1553155	Foxo3	forkhead box O3	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15308101
1553155	Foxo3	forkhead box O3	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:14978268
1553155	Foxo3	forkhead box O3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25264246
1553155	Foxo3	forkhead box O3	gene	MP:0009361	abnormal primordial ovarian follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18601916
1553155	Foxo3	forkhead box O3	gene	MP:0009361	abnormal primordial ovarian follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0009442	increased ovarian teratoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0009442	increased ovarian teratoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0009648	abnormal superovulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:18371339
1553155	Foxo3	forkhead box O3	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20220519	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20200310	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0012121	sclerocornea		IEA		N	RGD:5509061	20200310	MGI			
1553155	Foxo3	forkhead box O3	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:26061565
1553155	Foxo3	forkhead box O3	gene	MP:0012437	increased Harderian gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:17254969
1553155	Foxo3	forkhead box O3	gene	MP:0012736	abnormal polar body morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21347845
1553155	Foxo3	forkhead box O3	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:26061565
1553155	Foxo3	forkhead box O3	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:12855809
1553155	Foxo3	forkhead box O3	gene	MP:0031383	increased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:21347845
1553159	Yipf5	Yip1 domain family, member 5	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1553159	Yipf5	Yip1 domain family, member 5	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
1553159	Yipf5	Yip1 domain family, member 5	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20201231	MGI			
1553159	Yipf5	Yip1 domain family, member 5	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20200310	MGI			
1553159	Yipf5	Yip1 domain family, member 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553159	Yipf5	Yip1 domain family, member 5	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20211021	MGI			
1553159	Yipf5	Yip1 domain family, member 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553159	Yipf5	Yip1 domain family, member 5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1553164	Cenpc1	centromere protein C1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9448298
1553164	Cenpc1	centromere protein C1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9448298
1553164	Cenpc1	centromere protein C1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9448298
1553164	Cenpc1	centromere protein C1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9448298
1553164	Cenpc1	centromere protein C1	gene	MP:0014693	abnormal cell nucleus size		IAGP		N	RGD:5509061	20250710	MGI			PMID:9448298
1553165	Mlh3	mutL homolog 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091911
1553165	Mlh3	mutL homolog 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091911
1553165	Mlh3	mutL homolog 3	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091911
1553165	Mlh3	mutL homolog 3	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091911
1553165	Mlh3	mutL homolog 3	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091911
1553165	Mlh3	mutL homolog 3	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091911
1553165	Mlh3	mutL homolog 3	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091911
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114101
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114101
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0000913	abnormal brain development		IEA		N	RGD:5509061	20170330	MGI			
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114101
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0001326	retina degeneration		IEA		N	RGD:5509061	20170330	MGI			
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114101
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454088
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454088
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170330	MGI			
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19017726
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114101
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0005623	abnormal meninges morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0006309	decreased retina ganglion cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0008030	abnormal Cajal-Retzius cell morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0009026	abnormal brain pia mater morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114101
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:16458488
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114101
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114101
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0009959	abnormal cerebellar hemisphere morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:26306834
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0010098	abnormal retina blood vessel pattern		IEA		N	RGD:5509061	20170330	MGI			
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0010235	abnormal retina inner limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454088
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0010452	retina microaneurysm		IEA		N	RGD:5509061	20170330	MGI			
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19114101
1553166	Pomgnt1	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1553168	Slc27a1	solute carrier family 27 (fatty acid transporter), member 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14991074
1553168	Slc27a1	solute carrier family 27 (fatty acid transporter), member 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14991074
1553168	Slc27a1	solute carrier family 27 (fatty acid transporter), member 1	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14991074
1553168	Slc27a1	solute carrier family 27 (fatty acid transporter), member 1	gene	MP:0014998	abnormal glucose metabolism		IAGP		N	RGD:5509061	20260611	MGI			PMID:14991074
1553168	Slc27a1	solute carrier family 27 (fatty acid transporter), member 1	gene	MP:0031413	abnormal skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:14991074
1553168	Slc27a1	solute carrier family 27 (fatty acid transporter), member 1	gene	MP:0031617	abnormal skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:14991074
1553171	Gpr153	G protein-coupled receptor 153	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1553171	Gpr153	G protein-coupled receptor 153	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1553171	Gpr153	G protein-coupled receptor 153	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1553173	Tspan2	tetraspanin 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24038504
1553173	Tspan2	tetraspanin 2	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24038504
1553173	Tspan2	tetraspanin 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:24038504
1553173	Tspan2	tetraspanin 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:24038504
1553173	Tspan2	tetraspanin 2	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24038504
1553173	Tspan2	tetraspanin 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24038504
1553173	Tspan2	tetraspanin 2	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24038504
1553173	Tspan2	tetraspanin 2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24038504
1553173	Tspan2	tetraspanin 2	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20200310	MGI			PMID:24038504
1553174	Rab1b	RAB1B, member RAS oncogene family	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244655
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1117319
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416238
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000756	forelimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1955109
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:4120487
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:1117319
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8027772
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7349996
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416238
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8027772
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244655
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4120487
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244655
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1955109
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416238
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:1955109
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416238
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416238
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20221215	MGI			
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20221215	MGI			
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416238
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1955109
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20111116	MGI			
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8006678
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1955109
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:1383870
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:2432278
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:8281455
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416238
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4120487
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1955109
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1955109
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1955109
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5709840
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0003371	decreased circulating estrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:210748
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:3142758
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1117319
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0003806	abnormal nucleotide metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:210748
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244655
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:3947038
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:8390608
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1955109
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1117319
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0006411	upturned snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:7416238
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0008460	absent dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244655
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:1117319
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0009435	abnormal miniature inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244655
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16244655
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20170914	MGI			PMID:20643756
1553179	Vps54	VPS54 GARP complex subunit	gene	MP:0030140	facial muscle atrophy		IAGP		N	RGD:5509061	20171005	MGI			PMID:5709840
1553180	Dele1	DAP3 binding cell death enhancer 1	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20200514	MGI			
1553180	Dele1	DAP3 binding cell death enhancer 1	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20200514	MGI			
1553180	Dele1	DAP3 binding cell death enhancer 1	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20201231	MGI			
1553180	Dele1	DAP3 binding cell death enhancer 1	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20200514	MGI			
1553180	Dele1	DAP3 binding cell death enhancer 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20220811	MGI			
1553180	Dele1	DAP3 binding cell death enhancer 1	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1553180	Dele1	DAP3 binding cell death enhancer 1	gene	MP:0009453	enhanced contextual conditioning behavior		IEA		N	RGD:5509061	20211021	MGI			
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099459
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22040906
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22040906
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190815	MGI			PMID:27890709
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20190815	MGI			PMID:27890709
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20201231	MGI			
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190815	MGI			PMID:27890709
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099459
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22040906
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20190815	MGI			PMID:27890709
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20190815	MGI			PMID:27890709
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20190815	MGI			PMID:27890709
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099459
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22040906
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:16099459
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0003908	decreased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22040906
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20190815	MGI			PMID:27890709
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20240523	MGI			
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21890494
1553181	Sgce	sarcoglycan, epsilon	gene	MP:0012575	increased noradrenaline level		IAGP		N	RGD:5509061	20190815	MGI			PMID:27890709
1553182	Casp7	caspase 7	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16469926
1553182	Casp7	caspase 7	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16469926
1553182	Casp7	caspase 7	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16469926
1553182	Casp7	caspase 7	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:16469926
1553182	Casp7	caspase 7	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16469926
1553182	Casp7	caspase 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16469926
1553182	Casp7	caspase 7	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16469926
1553182	Casp7	caspase 7	gene	MP:0013502	decreased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16469926
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000141	abnormal vertebral body morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000282	abnormal interatrial septum morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000297	abnormal atrioventricular cushion morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000632	abnormal pineal gland morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000788	abnormal cerebral cortex morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0000963	fused dorsal root ganglion		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0002249	abnormal larynx morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0003105	abnormal heart atrium morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0003130	anal atresia		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0003262	intestinal/bowel diverticulum		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0003617	urinary bladder hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0003922	abnormal heart right atrium morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0004603	absent vertebral arch		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0006065	abnormal heart position or orientation		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0006093	arteriovenous malformation		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0006408	dorsal root ganglion hypoplasia		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0008128	abnormal brain internal capsule morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0010200	enlarged lymphatic vessel		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0010496	abnormal pectinate muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0010595	abnormal aortic valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0010912	herniated liver		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0011493	double ureter		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013826	absent hypoglossal canal		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013859	abnormal vitelline vein connection		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013878	abnormal ductus venosus valve topology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013913	absent costovertebral joint		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013924	abnormal dural venous sinus morphology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013937	decreased thyroid gland lobe number		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013952	retroesophageal left subclavian artery		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0014017	abnormal Wolffian duct connection		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0014019	embryo cyst		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20170504	MGI			
1553185	Ltap1	lipid transport auxiliary protein 1	gene	MP:0020500	persistent trigeminal artery		IEA		N	RGD:5509061	20180628	MGI			
1553186	Wdr74	WD repeat domain 74	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1553186	Wdr74	WD repeat domain 74	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553187	Mia	MIA SH3 domain containing	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11839810
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200310	MGI			
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20200310	MGI			
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0000685	abnormal immune system morphology		IEA		N	RGD:5509061	20200310	MGI			
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200310	MGI			
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0001790	abnormal immune system physiology		IEA		N	RGD:5509061	20200310	MGI			
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20200310	MGI			
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20200310	MGI			
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0005508	abnormal skeleton morphology		IEA		N	RGD:5509061	20200310	MGI			
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200310	MGI			
1553189	Crispld2	cysteine-rich secretory protein LCCL domain containing 2	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20576531
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20230119	MGI			
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20022947
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16311600
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20022947
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21941299
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20576531
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:20576531
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20200310	MGI			PMID:20576531
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16311600
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20576531
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20022947
1553192	Pdia3	protein disulfide isomerase associated 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20230119	MGI			
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20230119	MGI			
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20200310	MGI			PMID:15890782
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20200310	MGI			PMID:15890782
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18425126
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18425126
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18425126
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18425126
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18425126
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15890782
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18425126
1553193	Smchd1	SMC hinge domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1553197	Klc1	kinesin light chain 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20180215	MGI			
1553197	Klc1	kinesin light chain 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491391
1553197	Klc1	kinesin light chain 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10491391
1553197	Klc1	kinesin light chain 1	gene	MP:0003225	axonal dystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19420244
1553197	Klc1	kinesin light chain 1	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731448
1553197	Klc1	kinesin light chain 1	gene	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:19420244
1553197	Klc1	kinesin light chain 1	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:19420244
1553197	Klc1	kinesin light chain 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15731448
1553197	Klc1	kinesin light chain 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19420244
1553197	Klc1	kinesin light chain 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19420244
1553197	Klc1	kinesin light chain 1	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19420244
1553197	Klc1	kinesin light chain 1	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19420244
1553197	Klc1	kinesin light chain 1	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:21335237
1553199	Trim10	tripartite motif-containing 10	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1553199	Trim10	tripartite motif-containing 10	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20240523	MGI			
1553199	Trim10	tripartite motif-containing 10	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20210708	MGI			PMID:32343488
1553199	Trim10	tripartite motif-containing 10	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20240523	MGI			
1553199	Trim10	tripartite motif-containing 10	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1553201	Fmn1	formin 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:7517224
1553201	Fmn1	formin 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:9234242
1553201	Fmn1	formin 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:9848078
1553201	Fmn1	formin 1	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0000547	short limbs		IEA		N	RGD:5509061	20111116	MGI			
1553201	Fmn1	formin 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17554679
1553201	Fmn1	formin 1	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:15198975
1553201	Fmn1	formin 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20221027	MGI			PMID:34548488
1553201	Fmn1	formin 1	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:15198975
1553201	Fmn1	formin 1	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:19383632
1553201	Fmn1	formin 1	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20221027	MGI			PMID:34548488
1553201	Fmn1	formin 1	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17554679
1553201	Fmn1	formin 1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19383632
1553201	Fmn1	formin 1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1553201	Fmn1	formin 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15198975
1553201	Fmn1	formin 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17554679
1553201	Fmn1	formin 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15198975
1553201	Fmn1	formin 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7517224
1553201	Fmn1	formin 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15198975
1553201	Fmn1	formin 1	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20200310	MGI			PMID:17554679
1553201	Fmn1	formin 1	gene	MP:0003073	abnormal metacarpal bone morphology		IEA		N	RGD:5509061	20111116	MGI			
1553201	Fmn1	formin 1	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0003586	dilated ureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:19383632
1553201	Fmn1	formin 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:7517224
1553201	Fmn1	formin 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:9234242
1553201	Fmn1	formin 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:9848078
1553201	Fmn1	formin 1	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:9234242
1553201	Fmn1	formin 1	gene	MP:0004356	radius hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0004639	fused metacarpal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:19383632
1553201	Fmn1	formin 1	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17554679
1553201	Fmn1	formin 1	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0005353	abnormal patella morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0005371	limbs/digits/tail phenotype		IAGP		N	RGD:5509061	20221027	MGI			PMID:34548488
1553201	Fmn1	formin 1	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:17554679
1553201	Fmn1	formin 1	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:19383632
1553201	Fmn1	formin 1	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18560567
1553201	Fmn1	formin 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:19383632
1553201	Fmn1	formin 1	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:9234242
1553201	Fmn1	formin 1	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:2320577
1553201	Fmn1	formin 1	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0009728	abnormal calcaneum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17554679
1553201	Fmn1	formin 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1553201	Fmn1	formin 1	gene	MP:0011530	fused radius and ulna		IAGP		N	RGD:5509061	20200310	MGI			PMID:2997621
1553201	Fmn1	formin 1	gene	MP:0011797	blind ureter		IAGP		N	RGD:5509061	20200310	MGI			PMID:9234242
1553201	Fmn1	formin 1	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:34548488
1553201	Fmn1	formin 1	gene	MP:0014320	abnormal autopod rotation		IAGP		N	RGD:5509061	20240404	MGI			PMID:17554679
1553201	Fmn1	formin 1	gene	MP:0014320	abnormal autopod rotation		IAGP		N	RGD:5509061	20240404	MGI			PMID:2320577
1553205	Skor1	SKI family transcriptional corepressor 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20230601	MGI			
1553205	Skor1	SKI family transcriptional corepressor 1	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1553205	Skor1	SKI family transcriptional corepressor 1	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1553205	Skor1	SKI family transcriptional corepressor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040213
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040213
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040213
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040213
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040213
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540358
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540358
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040213
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540358
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11040213
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17540358
1553207	Dmrt1	doublesex and mab-3 related transcription factor 1	gene	MP:0031407	increased Sertoli cell proliferation		IAGP		N	RGD:5509061	20220630	MGI			PMID:11040213
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20240822	MGI			PMID:37341808
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221714
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16502419
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724733
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20240822	MGI			PMID:37341808
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000202	abnormal circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20220519	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17868088
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11350121
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597577
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724733
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17868088
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8988167
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20240822	MGI			PMID:37341808
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20220519	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000579	abnormal nail morphology		IEA		N	RGD:5509061	20220519	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652354
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12553906
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11350121
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724733
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17868088
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7729687
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11350121
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:7729687
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20260402	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20240822	MGI			PMID:37341808
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20111116	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0001565	abnormal circulating phosphate level		IEA		N	RGD:5509061	20260402	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17868088
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12221714
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20220519	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0002115	abnormal limb bone morphology		IEA		N	RGD:5509061	20111222	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20220519	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0003417	premature endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0004337	clavicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:14597577
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0004386	enlarged interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:8988167
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0004424	temporal bone hypoplasia		IAGP		N	RGD:5509061	20171207	MGI			PMID:12221714
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20220519	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20220519	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12553906
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0005270	abnormal zygomatic bone morphology		IEA		N	RGD:5509061	20220519	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0008430	short temporal bone squamous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:17868088
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20240822	MGI			PMID:37341808
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12553906
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11350121
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7729687
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20240822	MGI			PMID:37341808
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14724733
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0013546	cleft soft palate		IAGP		N	RGD:5509061	20240822	MGI			PMID:37341808
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:12221714
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:15030764
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0030350	premature coronal suture closure		IAGP		N	RGD:5509061	20251009	MGI			PMID:23354436
1553211	Twist1	twist basic helix-loop-helix transcription factor 1	gene	MP:0030356	premature lambdoid suture closure		IAGP		N	RGD:5509061	20171207	MGI			PMID:15030764
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553213	Fars2	phenylalanine-tRNA synthetase 2, mitochondrial	gene	MP:0014246	decreased cellular ATP level		IAGP		N	RGD:5509061	20240509	MGI			PMID:35794642
1553214	Stx16	syntaxin 16	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:17317779
1553214	Stx16	syntaxin 16	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200310	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200310	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20220811	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20220519	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1553214	Stx16	syntaxin 16	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1553215	Med31	mediator complex subunit 31	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:12955145
1553215	Med31	mediator complex subunit 31	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:12955145
1553215	Med31	mediator complex subunit 31	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12955145
1553215	Med31	mediator complex subunit 31	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12955145
1553215	Med31	mediator complex subunit 31	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12955145
1553215	Med31	mediator complex subunit 31	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553215	Med31	mediator complex subunit 31	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:20347762
1553217	Rdx	radixin	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068294
1553217	Rdx	radixin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068294
1553217	Rdx	radixin	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0004528	fused outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0004531	short outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0004533	fused inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0004536	short inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068294
1553217	Rdx	radixin	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068294
1553217	Rdx	radixin	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1553217	Rdx	radixin	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553217	Rdx	radixin	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12068294
1553217	Rdx	radixin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553217	Rdx	radixin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314067
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0008347	decreased gamma-delta T cell number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553218	Pole3	polymerase (DNA directed), epsilon 3 (p17 subunit)	gene	MP:0014180	abnormal thymus apoptosis		IAGP		N	RGD:5509061	20210128	MGI			PMID:32553171
1553219	Zfyve27	zinc finger, FYVE domain containing 27	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210617	MGI			PMID:33172474
1553219	Zfyve27	zinc finger, FYVE domain containing 27	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210617	MGI			PMID:33172474
1553219	Zfyve27	zinc finger, FYVE domain containing 27	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20210617	MGI			PMID:33172474
1553219	Zfyve27	zinc finger, FYVE domain containing 27	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20210617	MGI			PMID:33172474
1553219	Zfyve27	zinc finger, FYVE domain containing 27	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20210617	MGI			PMID:33172474
1553219	Zfyve27	zinc finger, FYVE domain containing 27	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20210617	MGI			PMID:33172474
1553219	Zfyve27	zinc finger, FYVE domain containing 27	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20210617	MGI			PMID:33172474
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761531
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761531
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761531
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17384153
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17384153
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0008327	abnormal corticotroph morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17761531
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17384153
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17384153
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0010809	abnormal club cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21160031
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0010899	abnormal pulmonary alveolar system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21160031
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0010943	abnormal bronchus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21160031
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20220519	MGI			
1553220	Rab27b	RAB27B, member RAS oncogene family	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20170720	MGI			PMID:17384153
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0000315	hemoglobinuria		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0001195	flaky skin		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20201022	MGI			
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0002708	nephrolithiasis		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0003622	ischuria		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0008822	decreased blood uric acid level		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0009552	urinary bladder obstruction		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0011419	erythrocyturia		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0011424	decreased urine uric acid level		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0011625	cystolithiasis		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0020400	cystinuria		IAGP		N	RGD:5509061	20170803	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0031479	increased urine xanthine level		IAGP		N	RGD:5509061	20230810	MGI			PMID:27138983
1553221	Mocs2	molybdenum cofactor synthesis 2	gene	MP:0031484	increased urine hypoxanthine level		IAGP		N	RGD:5509061	20230810	MGI			PMID:27138983
1553224	Dus2	dihydrouridine synthase 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200514	MGI			
1553224	Dus2	dihydrouridine synthase 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200514	MGI			
1553224	Dus2	dihydrouridine synthase 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20201022	MGI			
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:10639148
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12444148
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:12444148
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20200310	MGI			PMID:10899911
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:10899911
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717117
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:16861683
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:16984919
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:18493980
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16429160
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16861683
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18493980
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7859282
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12444148
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:7535475
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:11298831
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14663141
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10639148
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:11342578
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:15644489
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11342578
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15644489
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:23090995
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10452974
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:14645573
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20221215	MGI			
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:15644489
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10899911
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28636595
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:10532634
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:11376856
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:9015751
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21565393
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7859282
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:7535475
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:10491411
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20200310	MGI			PMID:10491411
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7859282
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22002608
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008639	decreased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22002608
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008639	decreased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7859282
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008639	decreased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20200310	MGI			PMID:9491891
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22002608
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7859282
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:9491891
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008655	decreased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:14693703
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008655	decreased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22002608
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008655	decreased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:7535475
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008655	decreased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:7859282
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:14663141
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:14693703
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18493980
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20457908
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22002608
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:29472103
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:7535475
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:7859282
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:9809553
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:10491411
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:14693703
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22002608
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:29472103
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:7535475
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16407889
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200310	MGI			PMID:22002608
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200310	MGI			PMID:7859282
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200310	MGI			PMID:9015751
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200310	MGI			PMID:9317135
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200310	MGI			PMID:9491891
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717117
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:7535475
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:16717117
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:10639148
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:22002608
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:18493980
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:10899911
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21565393
1553228	Casp4	caspase 4, apoptosis-related cysteine peptidase	gene	MP:0011081	decreased macrophage apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22002608
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0000640	adrenal gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20141003	MGI			
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0001748	increased circulating adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0002665	decreased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IEA		N	RGD:5509061	20141003	MGI			
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0005459	decreased percent body fat/body weight		IEA		N	RGD:5509061	20141003	MGI			
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0005661	decreased circulating adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0008294	abnormal adrenal gland zona fasciculata morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0008299	adrenal cortical hyperplasia		IEA		N	RGD:5509061	20141003	MGI			
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0009137	decreased brown fat lipid droplet number		IEA		N	RGD:5509061	20141003	MGI			
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0013565	abnormal adrenal gland capsule morphology		IAGP		N	RGD:5509061	20150305	MGI			PMID:17989225
1553230	Mc2r	melanocortin 2 receptor	gene	MP:0031391	increased locomotor activity		IEA		N	RGD:5509061	20220421	MGI			
1553231	Cnr2	cannabinoid receptor 2	gene	MP:0000414	alopecia		IEA		N	RGD:5509061	20111116	MGI			
1553231	Cnr2	cannabinoid receptor 2	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210520	MGI			
1553231	Cnr2	cannabinoid receptor 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1553231	Cnr2	cannabinoid receptor 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1553231	Cnr2	cannabinoid receptor 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10822068
1553231	Cnr2	cannabinoid receptor 2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1553231	Cnr2	cannabinoid receptor 2	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20210520	MGI			
1553231	Cnr2	cannabinoid receptor 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1553233	Tspan9	tetraspanin 9	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20210722	MGI			PMID:34048705
1553233	Tspan9	tetraspanin 9	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:34048705
1553233	Tspan9	tetraspanin 9	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1553233	Tspan9	tetraspanin 9	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:34048705
1553233	Tspan9	tetraspanin 9	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0000181	abnormal circulating LDL cholesterol level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0001553	abnormal circulating free fatty acids level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0001573	abnormal circulating alanine transaminase level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0006084	abnormal circulating phospholipid level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0008804	abnormal circulating amylase level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0010952	abnormal fatty acid beta-oxidation		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0013138	thin body		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0014146	decreased white adipose tissue mass		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0014605	dark liver		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0020868	decreased lipogenesis		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0030969	increased circulating adiponectin level		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553234	Plaat1	phospholipase A and acyltransferase 1	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20250605	MGI			PMID:37330992
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15989966
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15989966
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:15989966
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15989966
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15989966
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28360124
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0008830	abnormal nucleolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21228155
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0008830	abnormal nucleolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28360124
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15989966
1553236	Rrn3	RRN3 RNA polymerase I transcription factor homolog (yeast)	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15989966
1553237	Krt86	keratin 86	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20210128	MGI			
1553237	Krt86	keratin 86	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20201022	MGI			
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20201022	MGI			
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21970857
1553238	Tacstd2	tumor-associated calcium signal transducer 2	gene	MP:0012193	increased keratinocyte migration		IAGP		N	RGD:5509061	20141204	MGI			PMID:21970857
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733589
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733589
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733589
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733589
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733589
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733589
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733589
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10733589
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0014468	disorganized sperm mitochondrial sheath		IAGP		N	RGD:5509061	20240613	MGI			PMID:10733589
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20191226	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20200227	MGI			PMID:12801998
1553240	Nectin2	nectin cell adhesion molecule 2	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:12801998
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811913
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31218818
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001011	abnormal superior cervical ganglion morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811913
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001013	enlarged superior cervical ganglion		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811913
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001013	enlarged superior cervical ganglion		IAGP		N	RGD:5509061	20201217	MGI			PMID:31218818
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001017	abnormal stellate ganglion morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811913
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001017	abnormal stellate ganglion morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:31218818
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001752	abnormal hypothalamus secretion		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811913
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20180920	MGI			PMID:29321660
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002039	increased neuroblastoma incidence		IAGP		N	RGD:5509061	20201217	MGI			PMID:31218818
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180920	MGI			PMID:29321660
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201217	MGI			PMID:31218818
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201217	MGI			PMID:31218818
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002673	abnormal sperm number		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20160225	MGI			PMID:21799923
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0005250	decreased Sertoli cell number		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0008940	delayed balanopreputial separation		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0008975	delayed male fertility		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0009751	enhanced behavioral response to alcohol		IAGP		N	RGD:5509061	20160225	MGI			PMID:21799923
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0010052	increased grip strength		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0010232	delayed skin pigmentation appearance		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20201217	MGI			PMID:31218818
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20160915	MGI			PMID:24811761
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20160304	MGI			PMID:25955180
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:31218818
1553242	Alk	anaplastic lymphoma kinase	gene	MP:0014592	decreased gonadotropin-releasing hormone neuron number		IAGP		N	RGD:5509061	20241212	MGI			PMID:25955180
1553245	Iscu	iron-sulfur cluster assembly enzyme	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20230907	MGI			PMID:21165651
1553246	Art2b	ADP-ribosyltransferase 2b	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585549
1553246	Art2b	ADP-ribosyltransferase 2b	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585549
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20190718	MGI			PMID:27247960
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575564
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575564
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575564
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20190718	MGI			PMID:27247960
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575564
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20220505	MGI			PMID:30792275
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20190718	MGI			PMID:27247960
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:27247960
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575564
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575564
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22575564
1553247	Adgrl3	adhesion G protein-coupled receptor L3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:27247960
1553252	Mdfic	MyoD family inhibitor domain containing	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20220804	MGI			PMID:35235341
1553252	Mdfic	MyoD family inhibitor domain containing	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20220804	MGI			PMID:35235341
1553252	Mdfic	MyoD family inhibitor domain containing	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20220804	MGI			PMID:35235341
1553252	Mdfic	MyoD family inhibitor domain containing	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220804	MGI			PMID:35235341
1553252	Mdfic	MyoD family inhibitor domain containing	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20220804	MGI			PMID:35235341
1553252	Mdfic	MyoD family inhibitor domain containing	gene	MP:0003660	chylothorax		IAGP		N	RGD:5509061	20220804	MGI			PMID:35235341
1553252	Mdfic	MyoD family inhibitor domain containing	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220804	MGI			PMID:35235341
1553252	Mdfic	MyoD family inhibitor domain containing	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20220804	MGI			PMID:35235341
1553253	Nsun6	NOL1/NOP2/Sun domain family member 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:33330931
1553255	Klhl18	kelch-like 18	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1553255	Klhl18	kelch-like 18	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1553255	Klhl18	kelch-like 18	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1553255	Klhl18	kelch-like 18	gene	MP:0004415	abnormal cochlear nerve compound action potential		IAGP		N	RGD:5509061	20211021	MGI			PMID:34597341
1553255	Klhl18	kelch-like 18	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:34597341
1553255	Klhl18	kelch-like 18	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1553255	Klhl18	kelch-like 18	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20211021	MGI			
1553255	Klhl18	kelch-like 18	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20211021	MGI			PMID:34597341
1553256	Ranbp10	RAN binding protein 10	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19801445
1553256	Ranbp10	RAN binding protein 10	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1553256	Ranbp10	RAN binding protein 10	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20200310	MGI			
1553256	Ranbp10	RAN binding protein 10	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:19801445
1553256	Ranbp10	RAN binding protein 10	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19801445
1553256	Ranbp10	RAN binding protein 10	gene	MP:0003405	abnormal platelet shape		IAGP		N	RGD:5509061	20200310	MGI			PMID:19801445
1553256	Ranbp10	RAN binding protein 10	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20200310	MGI			
1553256	Ranbp10	RAN binding protein 10	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20200310	MGI			PMID:19801445
1553256	Ranbp10	RAN binding protein 10	gene	MP:0009446	abnormal platelet dense granule physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19801445
1553256	Ranbp10	RAN binding protein 10	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19801445
1553257	Zmynd8	zinc finger, MYND-type containing 8	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1553257	Zmynd8	zinc finger, MYND-type containing 8	gene	MP:0001539	decreased caudal vertebrae number		IEA		N	RGD:5509061	20200310	MGI			
1553257	Zmynd8	zinc finger, MYND-type containing 8	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20200310	MGI			
1553257	Zmynd8	zinc finger, MYND-type containing 8	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200310	MGI			
1553257	Zmynd8	zinc finger, MYND-type containing 8	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200310	MGI			
1553257	Zmynd8	zinc finger, MYND-type containing 8	gene	MP:0010093	decreased circulating magnesium level		IEA		N	RGD:5509061	20200310	MGI			
1553257	Zmynd8	zinc finger, MYND-type containing 8	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20230223	MGI			PMID:35857506
1553257	Zmynd8	zinc finger, MYND-type containing 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553258	Ttyh3	tweety family member 3	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1553258	Ttyh3	tweety family member 3	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169909
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20160310	MGI			PMID:26476408
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169909
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220811	MGI			
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20240523	MGI			
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20160310	MGI			PMID:26476408
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169909
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169909
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15169909
1553259	Ube2a	ubiquitin-conjugating enzyme E2A	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20160310	MGI			PMID:26476408
1553261	Cachd1	cache domain containing 1	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20211216	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0000035	abnormal membranous labyrinth morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20211216	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1553261	Cachd1	cache domain containing 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0003144	decreased otolith number		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0003149	abnormal tectorial membrane morphology		IAGP		N	RGD:5509061	20211216	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0003169	abnormal scala media morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20211216	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0004422	small temporal bone		IAGP		N	RGD:5509061	20211216	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20211216	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0004885	abnormal endolymph physiology		IAGP		N	RGD:5509061	20211216	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0004886	increased endolymph production		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0006012	dilated endolymphatic duct		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0006403	abnormal cochlear endolymph ionic homeostasis		IAGP		N	RGD:5509061	20211216	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553261	Cachd1	cache domain containing 1	gene	MP:0011238	abnormal inner ear development		IAGP		N	RGD:5509061	20211216	MGI			PMID:34388681
1553261	Cachd1	cache domain containing 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20211209	MGI			PMID:34388681
1553262	Tbc1d10c	TBC1 domain family, member 10c	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23109291
1553262	Tbc1d10c	TBC1 domain family, member 10c	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23109291
1553262	Tbc1d10c	TBC1 domain family, member 10c	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23109291
1553262	Tbc1d10c	TBC1 domain family, member 10c	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23109291
1553262	Tbc1d10c	TBC1 domain family, member 10c	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23109291
1553262	Tbc1d10c	TBC1 domain family, member 10c	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20200310	MGI			PMID:23109291
1553262	Tbc1d10c	TBC1 domain family, member 10c	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:23109291
1553262	Tbc1d10c	TBC1 domain family, member 10c	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23109291
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0004941	abnormal regulatory T cell morphology		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0008087	decreased T helper 1 cell number		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0010740	abnormal dendritic cell chemotaxis		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0013022	increased Ly6C high monocyte number		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553263	Extl1	exostosin-like glycosyltransferase 1	gene	MP:0020349	abnormal dendritic cell migration		IAGP		N	RGD:5509061	20240606	MGI			PMID:36656709
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20347813
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15825076
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015290
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384261
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431239
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0000765	abnormal tongue squamous epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20347813
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:20347813
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431239
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431239
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0001320	small pupil		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431239
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431239
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745808
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002009	preneoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15825076
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20347813
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015290
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20347813
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20347813
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002782	abnormal testes secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431239
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0003092	decreased cornea stroma thickness		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0003093	abnormal cornea anterior stroma morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0003285	gastric hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15825076
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431239
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22384261
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0003892	abnormal gastric gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15825076
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0004109	abnormal Sertoli cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0004137	abnormal gastric surface mucous cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15825076
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0004138	abnormal mucous neck cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15825076
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15825076
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0004140	abnormal gastric chief cell morphology		IAGP		N	RGD:5509061	20150312	MGI			PMID:15825076
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0004481	abnormal conjunctival epithelium morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491752
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:27027284
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0006307	abnormal seminiferous tubule size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0008521	abnormal Bowman membrane morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491752
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22745808
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0009612	thick epidermis suprabasal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22491752
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0009742	increased cornea stroma thickness		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0010203	focal ventral hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20347813
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0010792	abnormal stomach mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15825076
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10431239
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12015290
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0011697	lens vacuoles		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18243172
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0012101	acoria		IAGP		N	RGD:5509061	20150212	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0012110	increased hair follicle number		IAGP		N	RGD:5509061	20180607	MGI			PMID:22491752
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0012193	increased keratinocyte migration		IAGP		N	RGD:5509061	20141204	MGI			PMID:22491752
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0013026	decreased Ly6C low monocyte number		IAGP		N	RGD:5509061	20170413	MGI			PMID:27814941
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0013485	increased Paneth cell number		IAGP		N	RGD:5509061	20160310	MGI			PMID:22384261
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0013527	absent conjunctiva goblet cells		IAGP		N	RGD:5509061	20150219	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0013527	absent conjunctiva goblet cells		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0013754	abnormal ocular surface morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:21600198
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0013765	iris hyperplasia		IAGP		N	RGD:5509061	20150430	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0013795	abnormal colon goblet cell morphology		IAGP		N	RGD:5509061	20150806	MGI			PMID:12015290
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0014077	ectopic Paneth cells		IAGP		N	RGD:5509061	20160310	MGI			PMID:22384261
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0020855	decreased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0020862	increased cornea fragility		IAGP		N	RGD:5509061	20181101	MGI			PMID:17060454
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0030574	increased hair follicle cell proliferation		IAGP		N	RGD:5509061	20181129	MGI			PMID:22745808
1553264	Klf4	Kruppel-like transcription factor 4 (gut)	gene	MP:0030577	increased keratinocyte adhesion		IAGP		N	RGD:5509061	20180607	MGI			PMID:22491752
1553266	Ddx51	DEAD box helicase 51	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1553266	Ddx51	DEAD box helicase 51	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1553266	Ddx51	DEAD box helicase 51	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553270	Smug1	single-strand selective monofunctional uracil DNA glycosylase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1553270	Smug1	single-strand selective monofunctional uracil DNA glycosylase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1553270	Smug1	single-strand selective monofunctional uracil DNA glycosylase	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1553270	Smug1	single-strand selective monofunctional uracil DNA glycosylase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1553270	Smug1	single-strand selective monofunctional uracil DNA glycosylase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22447450
1553270	Smug1	single-strand selective monofunctional uracil DNA glycosylase	gene	MP:0014762	impaired base-excision repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:22447450
1553270	Smug1	single-strand selective monofunctional uracil DNA glycosylase	gene	MP:0014766	impaired mismatch repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:22447450
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21224394
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0003450	enlarged pancreas		IEA		N	RGD:5509061	20190502	MGI			
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553271	Fblim1	filamin binding LIM protein 1	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556421
1553273	Amigo2	adhesion molecule with Ig like domain 2	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:31693896
1553273	Amigo2	adhesion molecule with Ig like domain 2	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:31693896
1553273	Amigo2	adhesion molecule with Ig like domain 2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1553273	Amigo2	adhesion molecule with Ig like domain 2	gene	MP:0020376	abnormal starburst amacrine cell morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:31693896
1553275	Hoxc6	homeobox C6	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002345
1553275	Hoxc6	homeobox C6	gene	MP:0001881	abnormal mammary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002345
1553275	Hoxc6	homeobox C6	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002345
1553275	Hoxc6	homeobox C6	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11002345
1553275	Hoxc6	homeobox C6	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0004680	small xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1553275	Hoxc6	homeobox C6	gene	MP:0013711	abnormal inguinal mammary gland morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:11002345
1553275	Hoxc6	homeobox C6	gene	MP:0013712	abnormal thoracic mammary gland morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:11002345
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20201231	MGI			
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20170105	MGI			
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209834
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209834
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930907
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930907
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0003609	small scrotum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209834
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209834
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209834
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0005358	abnormal incisor morphology		IEA		N	RGD:5509061	20201231	MGI			
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209834
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21209834
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21930907
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:23213375
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553279	Hsp90aa1	heat shock protein 90, alpha (cytosolic), class A member 1	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20200213	MGI			PMID:31408169
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0010953	abnormal fatty acid oxidation		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553280	Hacl1	2-hydroxyacyl-CoA lyase 1	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20250807	MGI			PMID:28629946
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20240808	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0014871	decreased liver malondialdehyde level		IAGP		N	RGD:5509061	20260212	MGI			PMID:36983072
1553284	Mtfmt	mitochondrial methionyl-tRNA formyltransferase	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260716	MGI			PMID:36983072
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:32029872
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20200507	MGI			PMID:32029872
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20200507	MGI			PMID:32029872
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20160929	MGI			PMID:24728038
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20160929	MGI			PMID:24728038
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:24728038
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:32029872
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0011996	abnormal retina inner nuclear layer thickness		IAGP		N	RGD:5509061	20170504	MGI			PMID:26387839
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19117985
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0014117	increased pancreatic beta cell apoptosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:24728038
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0020087	increased susceptibility to non-insulin-dependent diabetes		IAGP		N	RGD:5509061	20160929	MGI			PMID:24728038
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0030006	decreased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:26387839
1553285	Tgfbi	transforming growth factor, beta induced	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:19117985
1553287	Pkn2	protein kinase N2	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1553287	Pkn2	protein kinase N2	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1553287	Pkn2	protein kinase N2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
1553287	Pkn2	protein kinase N2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0003874	absent pharyngeal arches		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1553287	Pkn2	protein kinase N2	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1553287	Pkn2	protein kinase N2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1553287	Pkn2	protein kinase N2	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0009328	delayed heart looping		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553287	Pkn2	protein kinase N2	gene	MP:0011702	abnormal fibroblast proliferation		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0011897	decreased circulating unsaturated transferrin level		IEA		N	RGD:5509061	20210128	MGI			
1553287	Pkn2	protein kinase N2	gene	MP:0012176	abnormal head development		IAGP		N	RGD:5509061	20171214	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0013925	abnormal vascular plexus formation		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0014138	abnormal germ layer morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553287	Pkn2	protein kinase N2	gene	MP:0014141	abnormal mesoderm morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:26774483
1553288	Zbed3	zinc finger, BED type containing 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20240523	MGI			
1553288	Zbed3	zinc finger, BED type containing 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20201112	MGI			PMID:28992324
1553288	Zbed3	zinc finger, BED type containing 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1553288	Zbed3	zinc finger, BED type containing 3	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20201112	MGI			PMID:28992324
1553288	Zbed3	zinc finger, BED type containing 3	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20201112	MGI			PMID:28992324
1553288	Zbed3	zinc finger, BED type containing 3	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20240523	MGI			
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15499555
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15499555
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500603
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15499555
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500603
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15499555
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9310465
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500603
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15499555
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500603
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0008053	abnormal NK cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15499555
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0008054	abnormal uterine NK cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15499555
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12219085
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500603
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500603
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0012529	abnormal decidua basalis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500603
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0012530	abnormal decidua capsularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9500603
1553290	Il11ra1	interleukin 11 receptor subunit alpha 1	gene	MP:0012530	abnormal decidua capsularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9679067
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20221215	MGI			
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20200310	MGI			
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0002174	abnormal gastrulation movements		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:15820682
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15820682
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:15820682
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:19379695
1553292	Smurf1	SMAD specific E3 ubiquitin protein ligase 1	gene	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:15820682
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167098
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12547917
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167098
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167098
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12103443
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167098
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167098
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167098
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:12547917
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167098
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12103443
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12103443
1553293	Apba1	amyloid beta precursor protein binding family A member 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17167098
1553294	Qpctl	glutaminyl-peptide cyclotransferase-like	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20230323	MGI			PMID:35314846
1553294	Qpctl	glutaminyl-peptide cyclotransferase-like	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20230323	MGI			PMID:35314846
1553294	Qpctl	glutaminyl-peptide cyclotransferase-like	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20200310	MGI			PMID:21900558
1553294	Qpctl	glutaminyl-peptide cyclotransferase-like	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20230323	MGI			PMID:35314846
1553296	Os9	amplified in osteosarcoma	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20201231	MGI			
1553296	Os9	amplified in osteosarcoma	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201231	MGI			
1553296	Os9	amplified in osteosarcoma	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20201231	MGI			
1553296	Os9	amplified in osteosarcoma	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20170105	MGI			
1553298	Tsn	translin	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20151112	MGI			PMID:18239274
1553298	Tsn	translin	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18719666
1553298	Tsn	translin	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0009286	increased abdominal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12944470
1553298	Tsn	translin	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20151112	MGI			PMID:18239274
1553298	Tsn	translin	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:12944470
1553300	Dcaf7	DDB1 and CUL4 associated factor 7	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
1553300	Dcaf7	DDB1 and CUL4 associated factor 7	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1553300	Dcaf7	DDB1 and CUL4 associated factor 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553300	Dcaf7	DDB1 and CUL4 associated factor 7	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20260402	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8046347
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0000618	small salivary gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:7541529
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0000653	abnormal sex gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001142	abnormal vagina orifice morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20200310	MGI			PMID:27534441
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20250508	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20250508	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:7541529
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:8339285
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:8828479
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002636	delayed vaginal opening		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002637	small uterus		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002669	abnormal scrotum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7541529
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002785	absent Leydig cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:19574395
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20260402	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:7541529
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0003642	absent seminal vesicle		IAGP		N	RGD:5509061	20200310	MGI			PMID:7541529
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:7541529
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8046347
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005128	decreased adrenocorticotropin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005130	decreased follicle stimulating hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005182	increased circulating estradiol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005186	increased circulating progesterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005188	small penis		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005189	abnormal anogenital distance		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7541529
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0005646	abnormal pituitary gland physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8046347
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:8046347
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:198666
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:8046347
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0008976	delayed female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0009007	short estrous cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0009012	short diestrus		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0009015	short proestrus		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0009047	short metestrus		IAGP		N	RGD:5509061	20200310	MGI			PMID:21368045
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1553302	Gnrh1	gonadotropin releasing hormone 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20260402	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0000277	abnormal heart shape		IEA		N	RGD:5509061	20210128	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20231207	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20221215	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1553303	Zc3h11a	zinc finger CCCH type containing 11A	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1553304	4933428G20Rik	RIKEN cDNA 4933428G20 gene	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1553304	4933428G20Rik	RIKEN cDNA 4933428G20 gene	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1553304	4933428G20Rik	RIKEN cDNA 4933428G20 gene	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1553306	Tnrc6c	trinucleotide repeat containing 6c	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1553306	Tnrc6c	trinucleotide repeat containing 6c	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28811219
1553306	Tnrc6c	trinucleotide repeat containing 6c	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:28811219
1553306	Tnrc6c	trinucleotide repeat containing 6c	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1553306	Tnrc6c	trinucleotide repeat containing 6c	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28811219
1553306	Tnrc6c	trinucleotide repeat containing 6c	gene	MP:0011142	abnormal lung-associated mesenchyme development		IAGP		N	RGD:5509061	20200310	MGI			PMID:28811219
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043238
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:8079170
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000215	absent erythrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867096
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000239	absent common myeloid progenitor cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867096
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867096
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395001
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867096
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994017
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867096
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043238
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043238
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163358
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163358
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914556
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8079170
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001586	abnormal erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001602	impaired myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001603	failure of myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739214
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043238
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043238
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8079170
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8079170
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15657291
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043238
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867096
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914556
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8079170
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002620	abnormal monocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8079170
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395001
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16163358
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395001
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914556
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994017
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994017
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867096
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994017
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005044	sepsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994017
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17994017
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005141	liver hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15146183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005141	liver hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8079170
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354487
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739214
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867096
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008113	abnormal macrophage differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008169	increased B-1b cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311598
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395001
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354487
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17588474
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354487
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739214
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15867096
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15914556
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18354487
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8079170
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011241	abnormal fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14739214
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23395001
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0014605	dark liver		IAGP		N	RGD:5509061	20250206	MGI			PMID:8896458
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:8079170
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:14739214
1553307	Spi1	Spi-1 proto-oncogene	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:14739214
1553310	Whrn	whirlin	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0000642	enlarged adrenal glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14098314
1553310	Whrn	whirlin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:14098314
1553310	Whrn	whirlin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14098314
1553310	Whrn	whirlin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1553310	Whrn	whirlin	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:14098314
1553310	Whrn	whirlin	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:14098314
1553310	Whrn	whirlin	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:14098314
1553310	Whrn	whirlin	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14098314
1553310	Whrn	whirlin	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0001745	increased circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14098314
1553310	Whrn	whirlin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20141003	MGI			
1553310	Whrn	whirlin	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0004362	cochlear hair cell degeneration		IEA		N	RGD:5509061	20111116	MGI			
1553310	Whrn	whirlin	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124769
1553310	Whrn	whirlin	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124769
1553310	Whrn	whirlin	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20332152
1553310	Whrn	whirlin	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124769
1553310	Whrn	whirlin	gene	MP:0004408	decreased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0004413	absent cochlear microphonics		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004416	absent cochlear nerve compound action potential		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004434	abnormal cochlear outer hair cell physiology		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004520	short vestibular hair cell stereocilia		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124769
1553310	Whrn	whirlin	gene	MP:0004524	short cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20161020	MGI			PMID:18160714
1553310	Whrn	whirlin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124769
1553310	Whrn	whirlin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326148
1553310	Whrn	whirlin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20332152
1553310	Whrn	whirlin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326148
1553310	Whrn	whirlin	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0004531	short outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20332152
1553310	Whrn	whirlin	gene	MP:0004536	short inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12124769
1553310	Whrn	whirlin	gene	MP:0004536	short inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17326148
1553310	Whrn	whirlin	gene	MP:0004536	short inner hair cell stereocilia		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004580	abnormal cochlear hair bundle transient lateral links morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0004910	decreased seminal vesicle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24211856
1553310	Whrn	whirlin	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:14098314
1553310	Whrn	whirlin	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:6034501
1553310	Whrn	whirlin	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1553310	Whrn	whirlin	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0006383	abnormal cochlear frequency tuning		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0006388	abnormal auditory summating potential		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553310	Whrn	whirlin	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24211856
1553310	Whrn	whirlin	gene	MP:0008455	abnormal retina rod cell inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24211856
1553310	Whrn	whirlin	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20502675
1553310	Whrn	whirlin	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:5538400
1553310	Whrn	whirlin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20161020	MGI			PMID:27117407
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553313	Ttll9	tubulin tyrosine ligase-like family, member 9	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:27257088
1553314	Med25	mediator complex subunit 25	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1553314	Med25	mediator complex subunit 25	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1553314	Med25	mediator complex subunit 25	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IEA		N	RGD:5509061	20201231	MGI			
1553314	Med25	mediator complex subunit 25	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1553314	Med25	mediator complex subunit 25	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1553314	Med25	mediator complex subunit 25	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1553314	Med25	mediator complex subunit 25	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1553314	Med25	mediator complex subunit 25	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553314	Med25	mediator complex subunit 25	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1553315	Tuba4a	tubulin, alpha 4A	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20200730	MGI			PMID:30760556
1553315	Tuba4a	tubulin, alpha 4A	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20200730	MGI			PMID:30760556
1553315	Tuba4a	tubulin, alpha 4A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200730	MGI			PMID:30760556
1553315	Tuba4a	tubulin, alpha 4A	gene	MP:0003405	abnormal platelet shape		IAGP		N	RGD:5509061	20200730	MGI			PMID:30760556
1553315	Tuba4a	tubulin, alpha 4A	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20200730	MGI			PMID:30760556
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20200310	MGI			PMID:8673132
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:8673132
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8673131
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9294109
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:11809728
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:8673132
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20200310	MGI			PMID:10021468
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0004089	dilated sarcoplasmic reticulum		IAGP		N	RGD:5509061	20200310	MGI			PMID:8673132
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10021468
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:8673132
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0004092	absent Z line		IAGP		N	RGD:5509061	20200310	MGI			PMID:8673132
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15598648
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15598648
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0006141	abnormal atrioventricular node conduction		IAGP		N	RGD:5509061	20200310	MGI			PMID:10021468
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20200310	MGI			PMID:8673132
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20200310	MGI			PMID:8673132
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20200310	MGI			PMID:10021468
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0010559	heart block		IAGP		N	RGD:5509061	20200310	MGI			PMID:10021468
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:8673132
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0031756	first degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:10021468
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0031757	second degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:10021468
1553318	Dmpk	dystrophia myotonica-protein kinase	gene	MP:0031762	third degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:10021468
1553326	Blcap	bladder cancer associated protein	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1553326	Blcap	bladder cancer associated protein	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1553329	Mt3	metallothionein 3	gene	MP:0000192	abnormal mineral level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006971
1553329	Mt3	metallothionein 3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14637104
1553329	Mt3	metallothionein 3	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14637104
1553329	Mt3	metallothionein 3	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14637104
1553329	Mt3	metallothionein 3	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388585
1553329	Mt3	metallothionein 3	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388585
1553329	Mt3	metallothionein 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388585
1553329	Mt3	metallothionein 3	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006971
1553329	Mt3	metallothionein 3	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14637104
1553329	Mt3	metallothionein 3	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9006971
1553329	Mt3	metallothionein 3	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:12388585
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0004806	absent germ cells		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20201002	MGI			PMID:32232159
1553334	Skp1	S-phase kinase-associated protein 1	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:32232159
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339551
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634774
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634774
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634774
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634774
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18466748
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634774
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339551
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21123569
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18466748
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IEA		N	RGD:5509061	20180215	MGI			
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18466748
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634774
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634774
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15634774
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339551
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19339551
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0008515	thin retina outer nuclear layer		IEA		N	RGD:5509061	20180215	MGI			
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20180215	MGI			
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:15634774
1553335	Cngb1	cyclic nucleotide gated channel beta 1	gene	MP:0014336	short retina rod cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:19339551
1553337	Echdc1	enoyl Coenzyme A hydratase domain containing 1	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
1553337	Echdc1	enoyl Coenzyme A hydratase domain containing 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
1553337	Echdc1	enoyl Coenzyme A hydratase domain containing 1	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
1553337	Echdc1	enoyl Coenzyme A hydratase domain containing 1	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
1553337	Echdc1	enoyl Coenzyme A hydratase domain containing 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20240425	MGI			PMID:38417553
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16192276
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16192276
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16192276
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:16192276
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16192276
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16192276
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16192276
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0014962	decreased brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:16192276
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0014967	increased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:16192276
1553340	Pisd	phosphatidylserine decarboxylase	gene	MP:0014968	decreased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260402	MGI			PMID:16192276
1553341	Slc16a4	solute carrier family 16 (monocarboxylic acid transporters), member 4	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1553343	Trmt1l	tRNA methyltransferase 1 like	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17198746
1553343	Trmt1l	tRNA methyltransferase 1 like	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17198746
1553343	Trmt1l	tRNA methyltransferase 1 like	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17198746
1553343	Trmt1l	tRNA methyltransferase 1 like	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:17198746
1553345	Anxa11	annexin A11	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0011975	neuronal cytoplasmic inclusions		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553345	Anxa11	annexin A11	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20250925	MGI			PMID:39755715
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28235781
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28235781
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:28235781
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210826	MGI			
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20200310	MGI			PMID:28235781
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:28235781
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0004084	abnormal cardiac muscle relaxation		IAGP		N	RGD:5509061	20200310	MGI			PMID:28235781
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0004183	abnormal sympathetic nervous system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28235781
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:28235781
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0010569	papillary muscle hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0010754	abnormal heart left ventricle pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0011915	increased heart left atrium weight		IAGP		N	RGD:5509061	20231221	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20200310	MGI			PMID:28235781
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20210826	MGI			
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0020419	decreased cardiac muscle relaxation		IAGP		N	RGD:5509061	20200310	MGI			PMID:26304555
1553347	Tnnc1	troponin C, cardiac/slow skeletal	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20231221	MGI			PMID:26304555
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17360554
1553352	Sumf1	sulfatase modifying factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161001
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16082726
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161001
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7545161
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18322191
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16082726
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161001
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0004942	abnormal B cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18322191
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161001
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18322191
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0010255	cortical cataract		IAGP		N	RGD:5509061	20210722	MGI			PMID:8560551
1553353	Ggta1	glycoprotein galactosyltransferase alpha 1, 3	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15161001
1553355	Rab6b	RAB6B, member RAS oncogene family	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20200310	MGI			
1553355	Rab6b	RAB6B, member RAS oncogene family	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20200310	MGI			
1553355	Rab6b	RAB6B, member RAS oncogene family	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20200310	MGI			
1553355	Rab6b	RAB6B, member RAS oncogene family	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20200310	MGI			
1553355	Rab6b	RAB6B, member RAS oncogene family	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200310	MGI			
1553355	Rab6b	RAB6B, member RAS oncogene family	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1553355	Rab6b	RAB6B, member RAS oncogene family	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200310	MGI			
1553355	Rab6b	RAB6B, member RAS oncogene family	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1553355	Rab6b	RAB6B, member RAS oncogene family	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1553356	Il17b	interleukin 17B	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20230914	MGI			PMID:36814913
1553356	Il17b	interleukin 17B	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008090	increased T-helper 2 cell number		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20230914	MGI			PMID:36814913
1553356	Il17b	interleukin 17B	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20230914	MGI			PMID:36814913
1553356	Il17b	interleukin 17B	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1553356	Il17b	interleukin 17B	gene	MP:0011078	increased macrophage cytokine production		IAGP		N	RGD:5509061	20230914	MGI			PMID:36814913
1553357	Or55b10	olfactory receptor family 55 subfamily B member 10	gene	MP:0001003	abnormal olfactory receptor morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:31378611
1553357	Or55b10	olfactory receptor family 55 subfamily B member 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19186165
1553357	Or55b10	olfactory receptor family 55 subfamily B member 10	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19186165
1553357	Or55b10	olfactory receptor family 55 subfamily B member 10	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20211021	MGI			PMID:31378611
1553360	Gimap4	GTPase, IMAP family member 4	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16569770
1553363	Dctd	dCMP deaminase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20251127	MGI			PMID:40324085
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20170105	MGI			
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20170105	MGI			
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0011939	increased food intake		IEA		N	RGD:5509061	20210128	MGI			
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0014434	decreased cytokine level		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553364	Leprot	leptin receptor overlapping transcript	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20240801	MGI			PMID:38716728
1553367	Tbc1d14	TBC1 domain family, member 14	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21118569
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200402	MGI			
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553369	Wdr45b	WD repeat domain 45B	gene	MP:0020365	increased brain iron level		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1553373	Klk10	kallikrein related-peptidase 10	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1553373	Klk10	kallikrein related-peptidase 10	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20240523	MGI			
1553373	Klk10	kallikrein related-peptidase 10	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20260402	MGI			
1553373	Klk10	kallikrein related-peptidase 10	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20240523	MGI			
1553373	Klk10	kallikrein related-peptidase 10	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1553373	Klk10	kallikrein related-peptidase 10	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20240523	MGI			
1553373	Klk10	kallikrein related-peptidase 10	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20240523	MGI			
1553373	Klk10	kallikrein related-peptidase 10	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20240523	MGI			
1553373	Klk10	kallikrein related-peptidase 10	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20240523	MGI			
1553374	Txndc11	thioredoxin domain containing 11	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1553374	Txndc11	thioredoxin domain containing 11	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1553374	Txndc11	thioredoxin domain containing 11	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20220519	MGI			
1553374	Txndc11	thioredoxin domain containing 11	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220519	MGI			
1553374	Txndc11	thioredoxin domain containing 11	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1553374	Txndc11	thioredoxin domain containing 11	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1553374	Txndc11	thioredoxin domain containing 11	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220519	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20170105	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20150430	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20151112	MGI			PMID:22580896
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20150430	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20150430	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0005285	decreased unsaturated fatty acids level		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21115496
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22580896
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20151112	MGI			PMID:22580896
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22580896
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20151112	MGI			PMID:22580896
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22580896
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22580896
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20150430	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20150430	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20211021	MGI			
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0012216	decreased plasmalogen level		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0012230	abnormal sphingolipid level		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20151112	MGI			PMID:22580896
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0020355	abnormal Sertoli cell barrier morphology		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553375	Sgms1	sphingomyelin synthase 1	gene	MP:0020356	abnormal Sertoli cell barrier function		IAGP		N	RGD:5509061	20190425	MGI			PMID:27788151
1553376	Pycard	PYD and CARD domain containing	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23219391
1553376	Pycard	PYD and CARD domain containing	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23219391
1553376	Pycard	PYD and CARD domain containing	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190255
1553376	Pycard	PYD and CARD domain containing	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19501000
1553376	Pycard	PYD and CARD domain containing	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16717117
1553376	Pycard	PYD and CARD domain containing	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1553376	Pycard	PYD and CARD domain containing	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457908
1553376	Pycard	PYD and CARD domain containing	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1553376	Pycard	PYD and CARD domain containing	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090995
1553376	Pycard	PYD and CARD domain containing	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1553376	Pycard	PYD and CARD domain containing	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407890
1553376	Pycard	PYD and CARD domain containing	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20351692
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008136	enlarged Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20180920	MGI			PMID:29263322
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457908
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090995
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457908
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15507117
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20180920	MGI			PMID:29263322
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20180920	MGI			PMID:29263322
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20351692
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002608
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002608
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008655	decreased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190255
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008655	decreased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008655	decreased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090995
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190255
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15507117
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407889
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407890
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16547271
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457908
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21600797
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002608
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090995
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15190255
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15507117
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407890
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16547271
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23090995
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:15507117
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546100
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002608
1553376	Pycard	PYD and CARD domain containing	gene	MP:0008896	increased IgG2c level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1553376	Pycard	PYD and CARD domain containing	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21565393
1553376	Pycard	PYD and CARD domain containing	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:20351692
1553377	Oas2	2'-5' oligoadenylate synthetase 2	gene	MP:0001881	abnormal mammary gland physiology		IAGP		N	RGD:5509061	20180517	MGI			PMID:29117179
1553377	Oas2	2'-5' oligoadenylate synthetase 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20180517	MGI			PMID:29117179
1553377	Oas2	2'-5' oligoadenylate synthetase 2	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20180517	MGI			PMID:29117179
1553377	Oas2	2'-5' oligoadenylate synthetase 2	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:29117179
1553377	Oas2	2'-5' oligoadenylate synthetase 2	gene	MP:0010174	decreased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20180517	MGI			PMID:29117179
1553377	Oas2	2'-5' oligoadenylate synthetase 2	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20180517	MGI			PMID:29117179
1553377	Oas2	2'-5' oligoadenylate synthetase 2	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20180517	MGI			PMID:29117179
1553379	Sccpdh	saccharopine dehydrogenase (putative)	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1553379	Sccpdh	saccharopine dehydrogenase (putative)	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1553379	Sccpdh	saccharopine dehydrogenase (putative)	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20240523	MGI			
1553380	Prdm15	PR domain containing 15	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20220519	MGI			
1553380	Prdm15	PR domain containing 15	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20220519	MGI			
1553380	Prdm15	PR domain containing 15	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1553380	Prdm15	PR domain containing 15	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0020515	abnormal visceral yolk sac endoderm morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553380	Prdm15	PR domain containing 15	gene	MP:0030324	abnormal anterior head development		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1553383	Pfn4	profilin family, member 4	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20230601	MGI			
1553383	Pfn4	profilin family, member 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0005573	increased pulmonary respiratory rate		IEA		N	RGD:5509061	20201022	MGI			
1553383	Pfn4	profilin family, member 4	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1553383	Pfn4	profilin family, member 4	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0009235	small sperm head		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0009325	necrospermia		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0012125	decreased bronchoconstrictive response		IEA		N	RGD:5509061	20211021	MGI			
1553383	Pfn4	profilin family, member 4	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0030949	abnormal Golgi vesicle transport		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20230209	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0031374	abnormal manchette assembly		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553383	Pfn4	profilin family, member 4	gene	MP:0031388	absent manchette		IAGP		N	RGD:5509061	20230216	MGI			PMID:35950913
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0003293	rectal hemorrhage		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553384	Muc13	mucin 13, epithelial transmembrane	gene	MP:0013799	abnormal intestinal goblet cell physiology		IAGP		N	RGD:5509061	20211202	MGI			PMID:21636645
1553387	Rtn2	reticulon 2 (Z-band associated protein)	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720795
1553387	Rtn2	reticulon 2 (Z-band associated protein)	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:19720795
1553389	Clk2	CDC-like kinase 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220811	MGI			
1553389	Clk2	CDC-like kinase 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1553389	Clk2	CDC-like kinase 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20201022	MGI			
1553389	Clk2	CDC-like kinase 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20160324	MGI			PMID:24458359
1553389	Clk2	CDC-like kinase 2	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20160324	MGI			PMID:24458359
1553389	Clk2	CDC-like kinase 2	gene	MP:0010953	abnormal fatty acid oxidation		IAGP		N	RGD:5509061	20160324	MGI			PMID:24458359
1553390	Rala	Ras like proto-oncogene A	gene	MP:0000026	abnormal inner ear morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0000534	abnormal ureter morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0000819	abnormal olfactory bulb morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0000826	abnormal third ventricle morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553390	Rala	Ras like proto-oncogene A	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553390	Rala	Ras like proto-oncogene A	gene	MP:0001015	small superior cervical ganglion		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0001917	intraventricular hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553390	Rala	Ras like proto-oncogene A	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0002947	increased hemangioma incidence		IEA		N	RGD:5509061	20210930	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553390	Rala	Ras like proto-oncogene A	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0003827	abnormal Wolffian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553390	Rala	Ras like proto-oncogene A	gene	MP:0004160	retroesophageal right subclavian artery		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0004268	abnormal optic stalk morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0005262	coloboma		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0006054	spinal hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0009493	abnormal cystic duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0009688	abnormal spinal cord central canal morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553390	Rala	Ras like proto-oncogene A	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553390	Rala	Ras like proto-oncogene A	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553390	Rala	Ras like proto-oncogene A	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0011380	enlarged brain ventricles		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0011513	abnormal vertebral artery morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553390	Rala	Ras like proto-oncogene A	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0013873	abnormal ductus venosus morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0013969	reduced sympathetic cervical ganglion size		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0014000	anastomosis between internal carotid artery and basilar artery		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0014019	embryo cyst		IEA		N	RGD:5509061	20170504	MGI			
1553390	Rala	Ras like proto-oncogene A	gene	MP:0014087	retrolental blood		IEA		N	RGD:5509061	20180628	MGI			
1553391	Impa2	inositol monophosphatase 2	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23205734
1553391	Impa2	inositol monophosphatase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201112	MGI			PMID:24554717
1553391	Impa2	inositol monophosphatase 2	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:23205734
1553392	Dek	DEK proto-oncogene	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223548
1553393	Ajuba	ajuba LIM protein	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1553393	Ajuba	ajuba LIM protein	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20201022	MGI			
1553393	Ajuba	ajuba LIM protein	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20201022	MGI			
1553393	Ajuba	ajuba LIM protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1553393	Ajuba	ajuba LIM protein	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728191
1553393	Ajuba	ajuba LIM protein	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1553393	Ajuba	ajuba LIM protein	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1553393	Ajuba	ajuba LIM protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20230209	MGI			PMID:35535434
1553394	Nsfl1c	NSFL1 (p97) cofactor (p47)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210128	MGI			
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210128	MGI			
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220811	MGI			
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404240
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404240
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0002932	abnormal joint morphology		IEA		N	RGD:5509061	20210128	MGI			
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404240
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404240
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404240
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17404240
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862162
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1553395	Ube2n	ubiquitin-conjugating enzyme E2N	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210520	MGI			
1553400	Sfxn5	sideroflexin 5	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20231207	MGI			
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170518
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0002791	steatorrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170518
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170518
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20170105	MGI			
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0009147	abnormal pancreatic acinar cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0009164	exocrine pancreas atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170518
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0009179	abnormal pancreatic alpha cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170518
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170518
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20170518
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0013139	moribund		IAGP		N	RGD:5509061	20141003	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0013220	increased pancreas apoptosis		IAGP		N	RGD:5509061	20160428	MGI			PMID:24453213
1553402	Sel1l	sel-1 suppressor of lin-12-like (C. elegans)	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20161013	MGI			PMID:20170518
1553404	Zfyve28	zinc finger, FYVE domain containing 28	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1553405	Akap3	A kinase anchor protein 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:31969357
1553405	Akap3	A kinase anchor protein 3	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:31969357
1553405	Akap3	A kinase anchor protein 3	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20220224	MGI			PMID:31969357
1553405	Akap3	A kinase anchor protein 3	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220224	MGI			PMID:31969357
1553405	Akap3	A kinase anchor protein 3	gene	MP:0009282	decreased hyperactivated sperm motility		IAGP		N	RGD:5509061	20220224	MGI			PMID:31969357
1553405	Akap3	A kinase anchor protein 3	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:31969357
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0000150	abnormal rib morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0001127	small ovary		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0002279	abnormal diaphragm morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0002652	thin myocardium		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0003105	abnormal heart atrium morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0003641	small lung		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0005477	increased circulating thyroxine level		IEA		N	RGD:5509061	20210128	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0009493	abnormal cystic duct morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0009494	abnormal biliary ductule morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0010439	abnormal hepatic vein morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0010912	herniated liver		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0011513	abnormal vertebral artery morphology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0012303	umbilical vein stenosis		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0013163	absent thyroid gland isthmus		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0013852	abnormal Mullerian duct topology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0013878	abnormal ductus venosus valve topology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0013967	abnormal infrahyoid muscle connection		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0013975	abnormal coronary sinus connection		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20180628	MGI			
1553407	Zmynd11	zinc finger, MYND domain containing 11	gene	MP:0014021	heterochrony		IEA		N	RGD:5509061	20180628	MGI			
1553411	Drc11	dynein regulatory complex subunit 11	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20201022	MGI			PMID:32588039
1553412	Angptl4	angiopoietin-like 4	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1553412	Angptl4	angiopoietin-like 4	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20200402	MGI			
1553412	Angptl4	angiopoietin-like 4	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1553412	Angptl4	angiopoietin-like 4	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1553412	Angptl4	angiopoietin-like 4	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19318355
1553412	Angptl4	angiopoietin-like 4	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832056
1553412	Angptl4	angiopoietin-like 4	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832056
1553412	Angptl4	angiopoietin-like 4	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832056
1553412	Angptl4	angiopoietin-like 4	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832056
1553412	Angptl4	angiopoietin-like 4	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1553412	Angptl4	angiopoietin-like 4	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19318355
1553412	Angptl4	angiopoietin-like 4	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832056
1553412	Angptl4	angiopoietin-like 4	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15505215
1553412	Angptl4	angiopoietin-like 4	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832056
1553412	Angptl4	angiopoietin-like 4	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553412	Angptl4	angiopoietin-like 4	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15505215
1553412	Angptl4	angiopoietin-like 4	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832056
1553412	Angptl4	angiopoietin-like 4	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1553412	Angptl4	angiopoietin-like 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832056
1553412	Angptl4	angiopoietin-like 4	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832056
1553412	Angptl4	angiopoietin-like 4	gene	MP:0011578	increased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1553412	Angptl4	angiopoietin-like 4	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609370
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20241121	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230601	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1553416	Tram1	translocating chain-associating membrane protein 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20210805	MGI			PMID:33716172
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20210520	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20210805	MGI			PMID:33716172
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210805	MGI			PMID:33716172
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20210128	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20260101	MGI			PMID:41120356
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0004857	abnormal heart weight		IEA		N	RGD:5509061	20260402	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20210520	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20210805	MGI			PMID:33716172
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20210805	MGI			PMID:33716172
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0013189	abnormal exploration in a new environment		IEA		N	RGD:5509061	20260402	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553418	Wdhd1	WD repeat and HMG-box DNA binding protein 1	gene	MP:0014762	impaired base-excision repair		IAGP		N	RGD:5509061	20260101	MGI			PMID:41120356
1553420	Prrx1	paired related homeobox 1	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000029	abnormal malleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198333
1553420	Prrx1	paired related homeobox 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198333
1553420	Prrx1	paired related homeobox 1	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000448	pointed snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000448	pointed snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000486	abnormal pulmonary trunk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1553420	Prrx1	paired related homeobox 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198333
1553420	Prrx1	paired related homeobox 1	gene	MP:0000548	long limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198333
1553420	Prrx1	paired related homeobox 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0000568	ectopic digits		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117820
1553420	Prrx1	paired related homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117820
1553420	Prrx1	paired related homeobox 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117820
1553420	Prrx1	paired related homeobox 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117820
1553420	Prrx1	paired related homeobox 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1553420	Prrx1	paired related homeobox 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198333
1553420	Prrx1	paired related homeobox 1	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0003869	ectopic cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117820
1553420	Prrx1	paired related homeobox 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1553420	Prrx1	paired related homeobox 1	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1553420	Prrx1	paired related homeobox 1	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004361	bowed ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004374	bowed radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0004443	absent supraoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004455	pterygoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004458	absent alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004460	alisphenoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004479	abnormal oval window morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004603	absent vertebral arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004679	xiphoid process foramen		IAGP		N	RGD:5509061	20181018	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004899	absent temporal bone squamous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0004899	absent temporal bone squamous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0004900	absent zygomatic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0005106	abnormal incus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0005107	abnormal stapes morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0006288	small otic capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0008374	abnormal malleus manubrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0008375	short malleus manubrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0008381	absent gonial bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20181101	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0009744	postaxial polydactyly		IAGP		N	RGD:5509061	20181101	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0009918	abnormal stylohyoid ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0010324	abnormal malleus processus brevis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0010464	abnormal aortic arch and aortic arch branch attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1553420	Prrx1	paired related homeobox 1	gene	MP:0010564	abnormal fetal ductus arteriosus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1553420	Prrx1	paired related homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10664157
1553420	Prrx1	paired related homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15117820
1553420	Prrx1	paired related homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0014281	hindlimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0020823	absent pubic symphysis		IAGP		N	RGD:5509061	20181018	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0030108	abnormal incudostapedial joint morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0030111	absent temporomandibular joint		IAGP		N	RGD:5509061	20171005	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0030297	outer ear hypoplasia		IAGP		N	RGD:5509061	20171102	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0030317	absent maxillary zygomatic process		IAGP		N	RGD:5509061	20171109	MGI			PMID:9729491
1553420	Prrx1	paired related homeobox 1	gene	MP:0030317	absent maxillary zygomatic process		IAGP		N	RGD:5509061	20171109	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0030406	absent stapes obturator foramen		IAGP		N	RGD:5509061	20171207	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0030407	abnormal stapes crus morpholgy		IAGP		N	RGD:5509061	20171207	MGI			PMID:7758948
1553420	Prrx1	paired related homeobox 1	gene	MP:0030456	abnormal odontoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0030471	abnormal ameloblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:9876178
1553420	Prrx1	paired related homeobox 1	gene	MP:0030862	absent triquetrum		IAGP		N	RGD:5509061	20181101	MGI			PMID:9882503
1553420	Prrx1	paired related homeobox 1	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:9729491
1553422	Tmed6	transmembrane p24 trafficking protein 6	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1553422	Tmed6	transmembrane p24 trafficking protein 6	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1553422	Tmed6	transmembrane p24 trafficking protein 6	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1553422	Tmed6	transmembrane p24 trafficking protein 6	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20200514	MGI			
1553422	Tmed6	transmembrane p24 trafficking protein 6	gene	MP:0004247	small pancreas		IEA		N	RGD:5509061	20200514	MGI			
1553422	Tmed6	transmembrane p24 trafficking protein 6	gene	MP:0013189	abnormal exploration in a new environment		IEA		N	RGD:5509061	20260402	MGI			
1553428	Fbxo43	F-box protein 43	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0009443	parthenogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553428	Fbxo43	F-box protein 43	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28723571
1553430	Tmem53	transmembrane protein 53	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0003840	abnormal coronal suture morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0011175	platyspondylia		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0030032	high forehead		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0030278	thick neurocranium		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0030417	craniofacial hyperostosis		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553430	Tmem53	transmembrane protein 53	gene	MP:0030469	optic canal stenosis		IAGP		N	RGD:5509061	20220203	MGI			PMID:33824347
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0030994	decreased adipose tissue glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:27815211
1553432	Ppp1r3g	protein phosphatase 1, regulatory subunit 3G	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:27815211
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20240523	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201231	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20230601	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0003099	retina detachment		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0005261	aniridia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20240523	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0006200	vitreous body deposition		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1553435	Stk35	serine/threonine kinase 35	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553435	Stk35	serine/threonine kinase 35	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:29970477
1553437	Selenot	selenoprotein T	gene	MP:0000774	decreased brain size		IEA		N	RGD:5509061	20231207	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20231207	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20231207	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20230119	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20231207	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23913443
1553437	Selenot	selenoprotein T	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23913443
1553437	Selenot	selenoprotein T	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230119	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23913443
1553437	Selenot	selenoprotein T	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20231207	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23913443
1553437	Selenot	selenoprotein T	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1553437	Selenot	selenoprotein T	gene	MP:0009167	increased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23913443
1553437	Selenot	selenoprotein T	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:23913443
1553437	Selenot	selenoprotein T	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20231207	MGI			
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14563650
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000187	abnormal triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15734843
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:11457855
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:11498544
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17517963
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16973879
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19342371
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12368209
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20200310	MGI			PMID:15044451
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:11457855
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:11498544
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12759258
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12660144
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178722
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16973879
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14563650
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001553	abnormal circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11457855
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15937515
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16501011
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:17517963
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12388746
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001885	mammary gland duct hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12368209
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001885	mammary gland duct hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:15044451
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:21467199
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:15802273
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12660144
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11498544
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002314	abnormal respiratory mechanics		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982927
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20210520	MGI			
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20260402	MGI			
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178722
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:17098833
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178722
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20200310	MGI			PMID:12167625
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:15044451
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17200204
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003180	abnormal pulmonary endothelial cell surface		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003191	abnormal cellular cholesterol metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:16603689
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003209	abnormal pulmonary elastic fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003416	premature bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003426	pulmonary interstitial fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11498544
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003442	decreased circulating glycerol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20200310	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003548	pulmonary hypertension		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:12651616
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15937515
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982927
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004001	decreased hepatocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16973879
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23652019
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004129	abnormal respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:11457855
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:11498544
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:11689550
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:15222744
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:15937515
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004150	absent caveolae		IAGP		N	RGD:5509061	20200310	MGI			PMID:23652019
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:12759258
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004697	abnormal thyroid follicular cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17202321
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20200310	MGI			PMID:15222744
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14563650
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14563650
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15734843
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12660144
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:14563650
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005360	urolithiasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12651616
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12651616
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:16973879
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11498544
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18178722
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12167625
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23652019
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20200310	MGI			PMID:17293479
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0006080	brain ischemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20200310	MGI			PMID:12388746
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0006429	abnormal hyaline cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15111495
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15734843
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20200310	MGI			PMID:11689550
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20210218	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982927
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008843	absent subcutaneous adipose tissue		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0008904	abnormal mammary fat pad morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009082	uterus cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:21467199
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15111495
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23652019
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15734843
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009122	decreased white fat cell lipid droplet size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15734843
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009251	enlarged endometrial glands		IAGP		N	RGD:5509061	20200310	MGI			PMID:21467199
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:16973879
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15044451
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12368209
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21467199
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:16973879
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:16750274
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010111	abnormal renal calcium reabsorption		IAGP		N	RGD:5509061	20200310	MGI			PMID:12651616
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:12631721
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:19342371
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010358	abnormal free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20200310	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010855	pulmonary hyperemia		IAGP		N	RGD:5509061	20200310	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010896	decreased lung compliance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010901	abnormal pulmonary alveolar parenchyma morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11457855
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010935	increased airway resistance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20200310	MGI			PMID:15734843
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0011044	increased lung elastance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849439
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15734843
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0011139	increased lung endothelial cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11498544
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15044451
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11457855
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11498544
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0013401	increased endometrial gland number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21467199
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:12177436
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0014864	increased circulating chylomicron triglyceride level		IAGP		N	RGD:5509061	20260219	MGI			PMID:11739396
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21203469
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0020415	abnormal fibroblast chemotaxis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17517963
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0020416	decreased fibroblast chemotaxis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17517963
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17517963
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0021159	increased heart right ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0021183	increased femoral compact bone area		IAGP		N	RGD:5509061	20220922	MGI			PMID:17550335
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0030876	abnormal costochondral joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16995819
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0030942	abnormal microtubule organizing center morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17517963
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0030974	enhanced gluconeogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:14690422
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0031220	increased circulating CXCL10 level		IAGP		N	RGD:5509061	20210218	MGI			PMID:16982844
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:22326219
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:12057923
1553438	Cav1	caveolin 1, caveolae protein	gene	MP:0031636	increased heart right ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:12177436
1553439	Fahd1	fumarylacetoacetate hydrolase domain containing 1	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:25575590
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20201029	MGI			PMID:32088381
1553440	Dynlrb1	dynein light chain roadblock-type 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553441	Cd6	CD6 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20170309	MGI			PMID:27909060
1553441	Cd6	CD6 antigen	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20170309	MGI			PMID:27909060
1553441	Cd6	CD6 antigen	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20170309	MGI			PMID:27909060
1553441	Cd6	CD6 antigen	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20170309	MGI			PMID:27909060
1553441	Cd6	CD6 antigen	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20170309	MGI			PMID:27909060
1553441	Cd6	CD6 antigen	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20170309	MGI			PMID:27909060
1553441	Cd6	CD6 antigen	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20170309	MGI			PMID:27909060
1553441	Cd6	CD6 antigen	gene	MP:0008169	increased B-1b cell number		IAGP		N	RGD:5509061	20170309	MGI			PMID:27909060
1553441	Cd6	CD6 antigen	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20170309	MGI			PMID:27909060
1553445	Arf1	ARF GTPase 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20151217	MGI			PMID:25305484
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20211021	MGI			
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20211021	MGI			
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20211021	MGI			
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20200402	MGI			
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20170105	MGI			
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553446	Atp6v1d	ATPase, H+ transporting, lysosomal V1 subunit D	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1553447	Gjc3	gap junction protein, gamma 3	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481432
1553447	Gjc3	gap junction protein, gamma 3	gene	MP:0004597	increased susceptibility to noise-induced hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481432
1553447	Gjc3	gap junction protein, gamma 3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20190502	MGI			
1553447	Gjc3	gap junction protein, gamma 3	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481432
1553447	Gjc3	gap junction protein, gamma 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481432
1553448	Sos2	SOS Ras/Rho guanine nucleotide exchange factor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10938118
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002343	abnormal lymph node cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002347	abnormal lymph node T cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002363	abnormal spleen marginal sinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302902
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18451854
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22538615
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002392	abnormal Peyer's patch T cell area morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23334413
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0002499	chronic inflammation		IEA		N	RGD:5509061	20111116	MGI			
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9825957
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17474155
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15302902
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17474155
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0003452	abnormal parotid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0003884	decreased macrophage cell number		IEA		N	RGD:5509061	20150702	MGI			
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17474155
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008082	increased single-positive T cell number		IEA		N	RGD:5509061	20150702	MGI			
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10520991
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008879	submandibular gland inflammation		IAGP		N	RGD:5509061	20141204	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0010740	abnormal dendritic cell chemotaxis		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0013367	parotid gland inflammation		IAGP		N	RGD:5509061	20141218	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0013558	abnormal exocrine gland morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:16473829
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:15302902
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0013649	decreased CD11b-high dendritic cell number		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0013655	decreased CD103-positive CD11b-low dendritic cell number		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1553451	Ccr7	C-C motif chemokine receptor 7	gene	MP:0014472	impaired B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:10520991
1553453	Fcrla	Fc receptor-like A	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20200310	MGI			
1553453	Fcrla	Fc receptor-like A	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20200310	MGI			
1553453	Fcrla	Fc receptor-like A	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1553453	Fcrla	Fc receptor-like A	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20200310	MGI			PMID:20668221
1553453	Fcrla	Fc receptor-like A	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200310	MGI			
1553453	Fcrla	Fc receptor-like A	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1553453	Fcrla	Fc receptor-like A	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210520	MGI			
1553453	Fcrla	Fc receptor-like A	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20668221
1553453	Fcrla	Fc receptor-like A	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20210520	MGI			
1553453	Fcrla	Fc receptor-like A	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20220519	MGI			
1553454	Cd300lg	CD300 molecule like family member G	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20200310	MGI			
1553454	Cd300lg	CD300 molecule like family member G	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1553454	Cd300lg	CD300 molecule like family member G	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20200310	MGI			
1553454	Cd300lg	CD300 molecule like family member G	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1553454	Cd300lg	CD300 molecule like family member G	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1553454	Cd300lg	CD300 molecule like family member G	gene	MP:0011939	increased food intake		IEA		N	RGD:5509061	20210128	MGI			
1553458	Cirbp	cold inducible RNA binding protein	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711815
1553458	Cirbp	cold inducible RNA binding protein	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711815
1553458	Cirbp	cold inducible RNA binding protein	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22711815
1553458	Cirbp	cold inducible RNA binding protein	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250213	MGI			PMID:22711815
1553461	Nrros	negative regulator of reactive oxygen species	gene	MP:0002409	decreased susceptibility to infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739962
1553461	Nrros	negative regulator of reactive oxygen species	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739962
1553461	Nrros	negative regulator of reactive oxygen species	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739962
1553461	Nrros	negative regulator of reactive oxygen species	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24739962
1553461	Nrros	negative regulator of reactive oxygen species	gene	MP:0014867	increased malondialdehyde level		IAGP		N	RGD:5509061	20260212	MGI			PMID:24739962
1553462	Btaf1	B-TFIID TATA-box binding protein associated factor 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21419221
1553462	Btaf1	B-TFIID TATA-box binding protein associated factor 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:21419221
1553462	Btaf1	B-TFIID TATA-box binding protein associated factor 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:21419221
1553462	Btaf1	B-TFIID TATA-box binding protein associated factor 1	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21419221
1553462	Btaf1	B-TFIID TATA-box binding protein associated factor 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21419221
1553462	Btaf1	B-TFIID TATA-box binding protein associated factor 1	gene	MP:0010503	myocardial trabeculae hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21419221
1553462	Btaf1	B-TFIID TATA-box binding protein associated factor 1	gene	MP:0012177	delayed head development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21419221
1553464	Papolg	poly(A) polymerase gamma	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20210128	MGI			
1553464	Papolg	poly(A) polymerase gamma	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1553464	Papolg	poly(A) polymerase gamma	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1553469	Rnasel	ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent)	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9351818
1553469	Rnasel	ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent)	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9351818
1553469	Rnasel	ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent)	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9351818
1553469	Rnasel	ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent)	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20220616	MGI			PMID:34343497
1553469	Rnasel	ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent)	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9351818
1553469	Rnasel	ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent)	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:10366581
1553469	Rnasel	ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent)	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:9351818
1553470	Hcar2	hydroxycarboxylic acid receptor 2	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20200514	MGI			
1553470	Hcar2	hydroxycarboxylic acid receptor 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12563315
1553472	Cyp20a1	cytochrome P450, family 20, subfamily a, polypeptide 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1553477	Mid1ip1	Mid1 interacting protein 1 (gastrulation specific G12-like (zebrafish))	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20220519	MGI			
1553477	Mid1ip1	Mid1 interacting protein 1 (gastrulation specific G12-like (zebrafish))	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20211021	MGI			
1553480	Usp47	ubiquitin specific peptidase 47	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1553480	Usp47	ubiquitin specific peptidase 47	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1553480	Usp47	ubiquitin specific peptidase 47	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1553480	Usp47	ubiquitin specific peptidase 47	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1553480	Usp47	ubiquitin specific peptidase 47	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19966869
1553481	Has3	hyaluronan synthase 3	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20250508	MGI			
1553481	Has3	hyaluronan synthase 3	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790861
1553481	Has3	hyaluronan synthase 3	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1553481	Has3	hyaluronan synthase 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1553484	Kif27	kinesin family member 27	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1553484	Kif27	kinesin family member 27	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1553484	Kif27	kinesin family member 27	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1553484	Kif27	kinesin family member 27	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1553484	Kif27	kinesin family member 27	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1553484	Kif27	kinesin family member 27	gene	MP:0002200	abnormal brain ventricular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1553484	Kif27	kinesin family member 27	gene	MP:0002236	abnormal internal nares morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1553484	Kif27	kinesin family member 27	gene	MP:0010752	impaired mucociliary clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1553484	Kif27	kinesin family member 27	gene	MP:0030113	maxillary sinus inflammation		IAGP		N	RGD:5509061	20171005	MGI			PMID:21746835
1553485	Gk2	glycerol kinase 2	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20190926	MGI			PMID:30662012
1553485	Gk2	glycerol kinase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190926	MGI			PMID:28852571
1553485	Gk2	glycerol kinase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190926	MGI			PMID:30662012
1553485	Gk2	glycerol kinase 2	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20190926	MGI			PMID:28852571
1553485	Gk2	glycerol kinase 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20190926	MGI			PMID:30662012
1553485	Gk2	glycerol kinase 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20190926	MGI			PMID:28852571
1553485	Gk2	glycerol kinase 2	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20190926	MGI			PMID:28852571
1553485	Gk2	glycerol kinase 2	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20190926	MGI			PMID:30662012
1553485	Gk2	glycerol kinase 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:28852571
1553485	Gk2	glycerol kinase 2	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:28852571
1553485	Gk2	glycerol kinase 2	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:30662012
1553485	Gk2	glycerol kinase 2	gene	MP:0014464	decreased sperm mitochondrial sheath size		IAGP		N	RGD:5509061	20240613	MGI			PMID:28852571
1553486	Cd300e	CD300E molecule	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1553486	Cd300e	CD300E molecule	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210520	MGI			
1553486	Cd300e	CD300E molecule	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210520	MGI			
1553486	Cd300e	CD300E molecule	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15860530
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29411926
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15860530
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20250911	MGI			PMID:37606043
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20250911	MGI			PMID:37606043
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24385426
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:29411926
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220721	MGI			PMID:29411926
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20250911	MGI			PMID:37606043
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0004184	abnormal baroreceptor physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15860530
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220721	MGI			PMID:29411926
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20250911	MGI			PMID:37606043
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20241121	MGI			
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0006243	impaired pupillary reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522242
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0008454	absent retina rod cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20250911	MGI			PMID:37606043
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0011021	abnormal circadian regulation of heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0011021	abnormal circadian regulation of heart rate		IAGP		N	RGD:5509061	20171012	MGI			PMID:15860530
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0011022	abnormal circadian regulation of systemic arterial blood pressure		IAGP		N	RGD:5509061	20171012	MGI			PMID:15860530
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0012315	impaired learning		IAGP		N	RGD:5509061	20250911	MGI			PMID:37606043
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20221215	MGI			
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:29411926
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20250911	MGI			PMID:37606043
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20250911	MGI			PMID:37606043
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0014413	decreased depression-related behavior		IAGP		N	RGD:5509061	20250911	MGI			PMID:37606043
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:10217146
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:15860530
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020468	abnormal circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:10217146
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020468	abnormal circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:23471982
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:10217146
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:10518585
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:10217146
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:10518585
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:12381662
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:11114194
1553489	Cry1	cryptochrome circadian regulator 1	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20171012	MGI			PMID:11114194
1553490	Celf6	CUGBP, Elav-like family member 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:23407934
1553490	Celf6	CUGBP, Elav-like family member 6	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:23407934
1553490	Celf6	CUGBP, Elav-like family member 6	gene	MP:0003462	abnormal response to novel odor		IAGP		N	RGD:5509061	20200310	MGI			PMID:23407934
1553490	Celf6	CUGBP, Elav-like family member 6	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23407934
1553490	Celf6	CUGBP, Elav-like family member 6	gene	MP:0010070	decreased serotonin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23407934
1553490	Celf6	CUGBP, Elav-like family member 6	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23407934
1553490	Celf6	CUGBP, Elav-like family member 6	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20200310	MGI			PMID:23407934
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220519	MGI			
1553491	Zc3h8	zinc finger CCCH type containing 8	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20211021	MGI			
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20200310	MGI			PMID:20333300
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21745644
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:21745644
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20200310	MGI			PMID:25157144
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:19160495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001404	no spontaneous movement		IAGP		N	RGD:5509061	20200310	MGI			PMID:16701208
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21745644
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:16701208
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:20333300
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:20333300
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21745644
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:21745644
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21745644
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002911	abnormal inhibitory postsynaptic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:16701208
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:19160495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:21745644
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20210826	MGI			PMID:32954490
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20200310	MGI			PMID:16701208
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20200310	MGI			PMID:16701208
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20210826	MGI			PMID:32954490
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0004143	muscle hypertonia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16701208
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:19160495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:19160495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19160495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20333300
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:16701208
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:20333300
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:21745644
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:19160495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20333300
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:19160495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:17418495
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16701208
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20333300
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:37261953
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0020422	decreased freezing behavior		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0020424	increased kindling response		IAGP		N	RGD:5509061	20210826	MGI			PMID:32954490
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0021010	impaired synaptic physiology		IAGP		N	RGD:5509061	20230921	MGI			PMID:37261953
1553492	Slc32a1	solute carrier family 32 (GABA vesicular transporter), member 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:19160495
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0000558	abnormal tibia morphology		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001391	abnormal tail movements		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0001938	delayed sexual maturation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004222	iris synechia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004284	abnormal Descemet membrane morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004373	bowed humerus		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004619	caudal vertebral fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004657	small sacral vertebrae		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004708	short lumbar vertebrae		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005108	abnormal ulna morphology		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0008297	retention of the adrenal gland x-zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0009199	abnormal external male genitalia morphology		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200310	MGI			
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23213448
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0014164	abnormal ciliary process morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0030048	sloping forehead		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0030167	decreased inner canthal distance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23166506
1553493	Cpap	centrosome assembly and centriole elongation protein	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24706806
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0001596	hypotension		IAGP		N	RGD:5509061	20141003	MGI			PMID:21972418
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21972418
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22648948
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21972418
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21972418
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22648948
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21972418
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0005628	decreased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21972418
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21972418
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20091762
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19307180
1553494	Oxsr1	oxidative-stress responsive 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20091762
1553496	Rpl7l1	ribosomal protein L7-like 1	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20200310	MGI			
1553496	Rpl7l1	ribosomal protein L7-like 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200310	MGI			
1553496	Rpl7l1	ribosomal protein L7-like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553496	Rpl7l1	ribosomal protein L7-like 1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1553496	Rpl7l1	ribosomal protein L7-like 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553497	Adgre1	adhesion G protein-coupled receptor E1	gene	MP:0002451	abnormal macrophage physiology		IEA		N	RGD:5509061	20141003	MGI			
1553497	Adgre1	adhesion G protein-coupled receptor E1	gene	MP:0003884	decreased macrophage cell number		IEA		N	RGD:5509061	20141003	MGI			
1553497	Adgre1	adhesion G protein-coupled receptor E1	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883173
1553497	Adgre1	adhesion G protein-coupled receptor E1	gene	MP:0005000	abnormal immune tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15883173
1553499	Rnf187	ring finger protein 187	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20240523	MGI			
1553499	Rnf187	ring finger protein 187	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1553499	Rnf187	ring finger protein 187	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20230601	MGI			
1553499	Rnf187	ring finger protein 187	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20240523	MGI			
1553499	Rnf187	ring finger protein 187	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210520	MGI			
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0010162	increased brain cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553501	Fuca1	fucosidase, alpha-L- 1, tissue	gene	MP:0011874	enlarged urinary bladder		IAGP		N	RGD:5509061	20200310	MGI			PMID:27491075
1553502	Ntf5	neurotrophin 5	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9973328
1553502	Ntf5	neurotrophin 5	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160421	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
1553502	Ntf5	neurotrophin 5	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
1553502	Ntf5	neurotrophin 5	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
1553502	Ntf5	neurotrophin 5	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
1553502	Ntf5	neurotrophin 5	gene	MP:0001021	small L4 dorsal root ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
1553502	Ntf5	neurotrophin 5	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995552
1553502	Ntf5	neurotrophin 5	gene	MP:0001083	small geniculate ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0001085	small petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
1553502	Ntf5	neurotrophin 5	gene	MP:0001085	small petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
1553502	Ntf5	neurotrophin 5	gene	MP:0001088	small nodose ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
1553502	Ntf5	neurotrophin 5	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
1553502	Ntf5	neurotrophin 5	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9973328
1553502	Ntf5	neurotrophin 5	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20210826	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
1553502	Ntf5	neurotrophin 5	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
1553502	Ntf5	neurotrophin 5	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
1553502	Ntf5	neurotrophin 5	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
1553502	Ntf5	neurotrophin 5	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
1553502	Ntf5	neurotrophin 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995552
1553502	Ntf5	neurotrophin 5	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20211021	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553502	Ntf5	neurotrophin 5	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:8674435
1553502	Ntf5	neurotrophin 5	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10681461
1553502	Ntf5	neurotrophin 5	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1553502	Ntf5	neurotrophin 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746324
1553502	Ntf5	neurotrophin 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7746325
1553504	B4galt3	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 3	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20241128	MGI			PMID:37901252
1553504	B4galt3	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 3	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20241128	MGI			PMID:37901252
1553504	B4galt3	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20241128	MGI			PMID:37901252
1553504	B4galt3	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20241128	MGI			PMID:37901252
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389239
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389239
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389239
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0004781	abnormal surfactant composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389239
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389239
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0008570	lipidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15071184
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17389239
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0010889	small alveolar lamellar bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0010891	increased alveolar lamellar body number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0010998	pulmonary alveolar proteinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23843985
1553506	Npc2	NPC intracellular cholesterol transporter 2	gene	MP:0031632	increased lung cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:23843985
1553508	Atl1	atlastin GTPase 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1553508	Atl1	atlastin GTPase 1	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20260402	MGI			
1553508	Atl1	atlastin GTPase 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11685207
1553508	Atl1	atlastin GTPase 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0005248	abnormal Harderian gland morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0009517	abnormal salivary gland duct morphology		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0010946	hyperpnea		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0012051	spasticity		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0014320	abnormal autopod rotation		IAGP		N	RGD:5509061	20240404	MGI			PMID:11685207
1553508	Atl1	atlastin GTPase 1	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553508	Atl1	atlastin GTPase 1	gene	MP:0031204	hindlimb paresis		IAGP		N	RGD:5509061	20230504	MGI			PMID:35348668
1553509	Fbxo11	F-box protein 11	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20181227	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20170720	MGI			PMID:25827072
1553509	Fbxo11	F-box protein 11	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20170720	MGI			PMID:25827072
1553509	Fbxo11	F-box protein 11	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20170720	MGI			PMID:25827072
1553509	Fbxo11	F-box protein 11	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20170105	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1553509	Fbxo11	F-box protein 11	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1553509	Fbxo11	F-box protein 11	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932191
1553509	Fbxo11	F-box protein 11	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20181227	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0003330	abnormal auditory tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0004411	decreased endocochlear potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0005287	narrow eye opening		IEA		N	RGD:5509061	20240523	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1553509	Fbxo11	F-box protein 11	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20170720	MGI			PMID:25827072
1553509	Fbxo11	F-box protein 11	gene	MP:0009603	absent keratohyalin granules		IAGP		N	RGD:5509061	20170720	MGI			PMID:25827072
1553509	Fbxo11	F-box protein 11	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210520	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170720	MGI			PMID:25827072
1553509	Fbxo11	F-box protein 11	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20221215	MGI			
1553509	Fbxo11	F-box protein 11	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20170921	MGI			PMID:17035249
1553509	Fbxo11	F-box protein 11	gene	MP:0030154	abnormal tympanic cavity morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0030226	middle ear polyps		IAGP		N	RGD:5509061	20171019	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0030226	middle ear polyps		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1553509	Fbxo11	F-box protein 11	gene	MP:0030410	middle ear effusion		IAGP		N	RGD:5509061	20171207	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0030410	middle ear effusion		IAGP		N	RGD:5509061	20171228	MGI			PMID:20057387
1553509	Fbxo11	F-box protein 11	gene	MP:0030413	tympanic membrane retraction		IAGP		N	RGD:5509061	20171207	MGI			PMID:12943368
1553509	Fbxo11	F-box protein 11	gene	MP:0030419	excessive cerumen		IAGP		N	RGD:5509061	20171207	MGI			PMID:12943368
1553510	Parp4	poly (ADP-ribose) polymerase family, member 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1553510	Parp4	poly (ADP-ribose) polymerase family, member 4	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1553510	Parp4	poly (ADP-ribose) polymerase family, member 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:15169895
1553510	Parp4	poly (ADP-ribose) polymerase family, member 4	gene	MP:0002759	abnormal caudal vertebrae morphology		IEA		N	RGD:5509061	20220811	MGI			
1553510	Parp4	poly (ADP-ribose) polymerase family, member 4	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1553510	Parp4	poly (ADP-ribose) polymerase family, member 4	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1553512	Pwp1	PWP1 homolog, endonuclein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553513	Tlr3	toll-like receptor 3	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18223009
1553513	Tlr3	toll-like receptor 3	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936008
1553513	Tlr3	toll-like receptor 3	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11607032
1553513	Tlr3	toll-like receptor 3	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233880
1553513	Tlr3	toll-like receptor 3	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16424225
1553513	Tlr3	toll-like receptor 3	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1553513	Tlr3	toll-like receptor 3	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12960379
1553513	Tlr3	toll-like receptor 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11607032
1553513	Tlr3	toll-like receptor 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625548
1553513	Tlr3	toll-like receptor 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11607032
1553513	Tlr3	toll-like receptor 3	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032677
1553513	Tlr3	toll-like receptor 3	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317384
1553513	Tlr3	toll-like receptor 3	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1553513	Tlr3	toll-like receptor 3	gene	MP:0003106	abnormal fear-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0003459	increased fear-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0003460	decreased fear-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18223009
1553513	Tlr3	toll-like receptor 3	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032677
1553513	Tlr3	toll-like receptor 3	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21220319
1553513	Tlr3	toll-like receptor 3	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1553513	Tlr3	toll-like receptor 3	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18032677
1553513	Tlr3	toll-like receptor 3	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782847
1553513	Tlr3	toll-like receptor 3	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1553513	Tlr3	toll-like receptor 3	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713712
1553513	Tlr3	toll-like receptor 3	gene	MP:0008561	decreased tumor necrosis factor secretion		IEA		N	RGD:5509061	20151015	MGI			
1553513	Tlr3	toll-like receptor 3	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20200423	MGI			PMID:16985170
1553513	Tlr3	toll-like receptor 3	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20180125	MGI			PMID:28970238
1553513	Tlr3	toll-like receptor 3	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16517751
1553513	Tlr3	toll-like receptor 3	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936008
1553513	Tlr3	toll-like receptor 3	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936008
1553513	Tlr3	toll-like receptor 3	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16424225
1553513	Tlr3	toll-like receptor 3	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936008
1553513	Tlr3	toll-like receptor 3	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16936008
1553513	Tlr3	toll-like receptor 3	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1553513	Tlr3	toll-like receptor 3	gene	MP:0009167	increased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357791
1553513	Tlr3	toll-like receptor 3	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19239422
1553513	Tlr3	toll-like receptor 3	gene	MP:0009669	abnormal postimplantation uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19239422
1553513	Tlr3	toll-like receptor 3	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993594
1553513	Tlr3	toll-like receptor 3	gene	MP:0011079	decreased macrophage cytokine production		IEA		N	RGD:5509061	20151015	MGI			
1553513	Tlr3	toll-like receptor 3	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18490751
1553513	Tlr3	toll-like receptor 3	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:14993594
1553513	Tlr3	toll-like receptor 3	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1553513	Tlr3	toll-like receptor 3	gene	MP:0031023	decreased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:18490751
1553513	Tlr3	toll-like receptor 3	gene	MP:0031040	increased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:16936008
1553513	Tlr3	toll-like receptor 3	gene	MP:0031079	increased circulating troponin I level		IAGP		N	RGD:5509061	20200618	MGI			PMID:16936008
1553514	Cpm	carboxypeptidase M	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20231207	MGI			
1553514	Cpm	carboxypeptidase M	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20231207	MGI			
1553514	Cpm	carboxypeptidase M	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20231207	MGI			
1553514	Cpm	carboxypeptidase M	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20250508	MGI			
1553514	Cpm	carboxypeptidase M	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20231207	MGI			
1553514	Cpm	carboxypeptidase M	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20231207	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20240523	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20250508	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20260402	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20240523	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0011045	decreased lung elastance		IEA		N	RGD:5509061	20260402	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1553517	Gnl2	guanine nucleotide binding protein nucleolar 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20260402	MGI			
1553518	Ecm1	extracellular matrix protein 1	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1553518	Ecm1	extracellular matrix protein 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21217760
1553518	Ecm1	extracellular matrix protein 1	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21217760
1553518	Ecm1	extracellular matrix protein 1	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:21217760
1553518	Ecm1	extracellular matrix protein 1	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21217760
1553518	Ecm1	extracellular matrix protein 1	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21217760
1553518	Ecm1	extracellular matrix protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553520	Ndufv1	NADH:ubiquinone oxidoreductase core subunit V1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1553520	Ndufv1	NADH:ubiquinone oxidoreductase core subunit V1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1553520	Ndufv1	NADH:ubiquinone oxidoreductase core subunit V1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1553520	Ndufv1	NADH:ubiquinone oxidoreductase core subunit V1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1553520	Ndufv1	NADH:ubiquinone oxidoreductase core subunit V1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553520	Ndufv1	NADH:ubiquinone oxidoreductase core subunit V1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144095
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144095
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22773818
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144095
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144095
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144095
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144095
1553522	Havcr1	hepatitis A virus cellular receptor 1	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22144095
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0000015	abnormal ear pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0005101	abnormal ciliary body pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0005102	abnormal iris pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20220519	MGI			
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0006159	ocular albinism		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0008731	abnormal hair shaft melanin granule morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0009273	abnormal hair shaft melanin granule shape		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0009385	abnormal dermal pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0009387	abnormal epidermal pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18424845
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20200310	MGI			
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20260402	MGI			
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0012122	abnormal iris transillumination		IEA		N	RGD:5509061	20200310	MGI			
1553523	Slc24a5	solute carrier family 24, member 5	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20200310	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20260219	MGI			PMID:39383878
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20260219	MGI			PMID:39383878
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20260219	MGI			PMID:39383878
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20260219	MGI			PMID:39383878
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20260219	MGI			PMID:39383878
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0004156	abnormal QT variability		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20260219	MGI			PMID:39383878
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0011179	decreased erythroblast number		IAGP		N	RGD:5509061	20260219	MGI			PMID:39383878
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:12727891
1553525	Parp2	poly (ADP-ribose) polymerase family, member 2	gene	MP:0021086	decreased DNA replication		IAGP		N	RGD:5509061	20260219	MGI			PMID:39383878
1553526	Wdr62	WD repeat domain 62	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31197141
1553526	Wdr62	WD repeat domain 62	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20200310	MGI			
1553526	Wdr62	WD repeat domain 62	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:31197141
1553526	Wdr62	WD repeat domain 62	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20200310	MGI			
1553526	Wdr62	WD repeat domain 62	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20200310	MGI			
1553526	Wdr62	WD repeat domain 62	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:31197141
1553526	Wdr62	WD repeat domain 62	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20200310	MGI			
1553526	Wdr62	WD repeat domain 62	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:31197141
1553526	Wdr62	WD repeat domain 62	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31197141
1553526	Wdr62	WD repeat domain 62	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31197141
1553526	Wdr62	WD repeat domain 62	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1553526	Wdr62	WD repeat domain 62	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1553526	Wdr62	WD repeat domain 62	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0009762	abnormal mitotic spindle assembly checkpoint		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:31197141
1553526	Wdr62	WD repeat domain 62	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:24875059
1553526	Wdr62	WD repeat domain 62	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31197141
1553526	Wdr62	WD repeat domain 62	gene	MP:0020066	abnormal neocortex size		IAGP		N	RGD:5509061	20200310	MGI			PMID:31197141
1553526	Wdr62	WD repeat domain 62	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210923	MGI			PMID:34059773
1553526	Wdr62	WD repeat domain 62	gene	MP:0031375	abnormal manchette disassembly		IAGP		N	RGD:5509061	20220407	MGI			PMID:34059773
1553528	Masp2	MBL associated serine protease 2	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:17142762
1553528	Masp2	MBL associated serine protease 2	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502512
1553528	Masp2	MBL associated serine protease 2	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502512
1553528	Masp2	MBL associated serine protease 2	gene	MP:0009062	impaired lectin complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:21502512
1553530	Zfp641	zinc finger protein 641	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1553530	Zfp641	zinc finger protein 641	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20221215	MGI			
1553530	Zfp641	zinc finger protein 641	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20221215	MGI			
1553530	Zfp641	zinc finger protein 641	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20221215	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12759446
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12759446
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651530
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943436
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943436
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943436
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18423204
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:18423204
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943436
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943436
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001213	abnormal skin cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20201022	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651530
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:20689803
1553531	Rac1	Rac family small GTPase 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1553531	Rac1	Rac family small GTPase 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20201022	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943436
1553531	Rac1	Rac family small GTPase 1	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20689803
1553531	Rac1	Rac family small GTPase 1	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943436
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651530
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943436
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003885	abnormal rostral-caudal body axis extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651530
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20689803
1553531	Rac1	Rac family small GTPase 1	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0004032	abnormal interventricular groove morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1553531	Rac1	Rac family small GTPase 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1553531	Rac1	Rac family small GTPase 1	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12759446
1553531	Rac1	Rac family small GTPase 1	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20689803
1553531	Rac1	Rac family small GTPase 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651530
1553531	Rac1	Rac family small GTPase 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16943436
1553531	Rac1	Rac family small GTPase 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651530
1553531	Rac1	Rac family small GTPase 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20180118	MGI			PMID:25079357
1553531	Rac1	Rac family small GTPase 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008222	decreased hippocampal commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12759446
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12759446
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20180118	MGI			PMID:25079357
1553531	Rac1	Rac family small GTPase 1	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0010498	abnormal interventricular septum muscular part morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0010682	abnormal hair follicle infundibulum morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20689803
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14564011
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20689803
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20689803
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12759446
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011190	thick embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:10030666
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011255	abnormal anterior visceral endoderm cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20689803
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0011805	decreased cell migration		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20689803
1553531	Rac1	Rac family small GTPase 1	gene	MP:0012515	abnormal heart apex morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:33804107
1553531	Rac1	Rac family small GTPase 1	gene	MP:0012515	abnormal heart apex morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:25315346
1553531	Rac1	Rac family small GTPase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1553531	Rac1	Rac family small GTPase 1	gene	MP:0013377	abnormal sebocyte number		IAGP		N	RGD:5509061	20141218	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150219	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:18423204
1553531	Rac1	Rac family small GTPase 1	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0020446	increased NAD(P)H oxidase activity		IAGP		N	RGD:5509061	20170914	MGI			PMID:16651530
1553531	Rac1	Rac family small GTPase 1	gene	MP:0030538	abnormal notochordal plate morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1553531	Rac1	Rac family small GTPase 1	gene	MP:0030919	absent hair follicle bulb		IAGP		N	RGD:5509061	20181220	MGI			PMID:16081735
1553531	Rac1	Rac family small GTPase 1	gene	MP:0031526	thin right ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:25315346
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20200310	MGI			PMID:27917469
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27917469
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20240314	MGI			
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20200310	MGI			PMID:27917469
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27917469
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20200310	MGI			PMID:23791195
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23791195
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:27917469
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27917469
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27917469
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:27917469
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:27917469
1553533	Syde1	synapse defective 1, Rho GTPase, homolog 1 (C. elegans)	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1553534	Nudcd1	NudC domain containing 1	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20260402	MGI			
1553534	Nudcd1	NudC domain containing 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:30254094
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0001729	impaired embryo implantation		IAGP		N	RGD:5509061	20220120	MGI			PMID:31875883
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220120	MGI			PMID:31875883
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220120	MGI			PMID:31875883
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:23973919
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:23973919
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:24553140
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849965
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24553140
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:30254094
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20220120	MGI			PMID:31875883
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849966
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23973919
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23973919
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:23973919
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849965
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:30254094
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200310	MGI			PMID:24553140
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849965
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008684	increased interleukin-18 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849965
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008800	increased small intestinal crypt cell apoptosis		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008885	increased enterocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:30254094
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0008923	thoracoschisis		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23973919
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0010439	abnormal hepatic vein morphology		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0010490	abnormal inferior vena cava valve morphology		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0011078	increased macrophage cytokine production		IAGP		N	RGD:5509061	20200310	MGI			PMID:24553140
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849965
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23973919
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013830	abnormal intrathoracic topology of vagus nerve		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013840	absent segment of posterior cerebral artery		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013936	abnormal thymus topology		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0013986	abnormal vitelline vein topology		IEA		N	RGD:5509061	20200310	MGI			
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20231221	MGI			PMID:36198790
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0014431	increased chemokine level		IAGP		N	RGD:5509061	20260219	MGI			PMID:23973919
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0014437	increased interleukin level		IAGP		N	RGD:5509061	20260219	MGI			PMID:23973919
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849965
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849965
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:18849966
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:22258505
1553543	Atg16l1	autophagy related 16 like 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:24553140
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18505822
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:18505822
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20250508	MGI			
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20250508	MGI			
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20250508	MGI			
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20250508	MGI			
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:18505822
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20250508	MGI			
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18505822
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18505822
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:18505822
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:18505822
1553545	Kremen1	kringle containing transmembrane protein 1	gene	MP:0020080	increased bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:18505822
1553546	Krt4	keratin 4	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:16858417
1553546	Krt4	keratin 4	gene	MP:0000466	esophageal epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727004
1553546	Krt4	keratin 4	gene	MP:0000468	abnormal esophageal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727004
1553546	Krt4	keratin 4	gene	MP:0000471	abnormal stomach epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727004
1553546	Krt4	keratin 4	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16858417
1553546	Krt4	keratin 4	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727004
1553546	Krt4	keratin 4	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727004
1553546	Krt4	keratin 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16858417
1553546	Krt4	keratin 4	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727004
1553546	Krt4	keratin 4	gene	MP:0003745	abnormal oral mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16858417
1553546	Krt4	keratin 4	gene	MP:0003751	oral leukoplakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16858417
1553546	Krt4	keratin 4	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9727004
1553546	Krt4	keratin 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16858417
1553546	Krt4	keratin 4	gene	MP:0020854	increased cornea epithelium thickness		IAGP		N	RGD:5509061	20181101	MGI			PMID:9727004
1553546	Krt4	keratin 4	gene	MP:0020857	cornea epithelium hyperplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:9727004
1553549	Tiprl	TIP41, TOR signalling pathway regulator-like (S. cerevisiae)	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20201231	MGI			
1553549	Tiprl	TIP41, TOR signalling pathway regulator-like (S. cerevisiae)	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20200310	MGI			
1553549	Tiprl	TIP41, TOR signalling pathway regulator-like (S. cerevisiae)	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1553549	Tiprl	TIP41, TOR signalling pathway regulator-like (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553549	Tiprl	TIP41, TOR signalling pathway regulator-like (S. cerevisiae)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210128	MGI			
1553549	Tiprl	TIP41, TOR signalling pathway regulator-like (S. cerevisiae)	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210826	MGI			
1553551	Casr	calcium-sensing receptor	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517179
1553551	Casr	calcium-sensing receptor	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0000069	kyphoscoliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22527485
1553551	Casr	calcium-sensing receptor	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0000195	decreased circulating calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517179
1553551	Casr	calcium-sensing receptor	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22527485
1553551	Casr	calcium-sensing receptor	gene	MP:0001102	small superior vagus ganglion		IEA		N	RGD:5509061	20221103	MGI			
1553551	Casr	calcium-sensing receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517179
1553551	Casr	calcium-sensing receptor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517179
1553551	Casr	calcium-sensing receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:22527485
1553551	Casr	calcium-sensing receptor	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1553551	Casr	calcium-sensing receptor	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20221103	MGI			
1553551	Casr	calcium-sensing receptor	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22527485
1553551	Casr	calcium-sensing receptor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517179
1553551	Casr	calcium-sensing receptor	gene	MP:0002902	decreased urine phosphate level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0002905	decreased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0002986	decreased urine calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0002986	decreased urine calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0003112	enlarged parathyroid gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0003114	pigmented parathyroid gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517179
1553551	Casr	calcium-sensing receptor	gene	MP:0003195	calcinosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0003199	calcified muscle		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553551	Casr	calcium-sensing receptor	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517179
1553551	Casr	calcium-sensing receptor	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0003493	parathyroid gland hyperplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22094462
1553551	Casr	calcium-sensing receptor	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20221103	MGI			
1553551	Casr	calcium-sensing receptor	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22094462
1553551	Casr	calcium-sensing receptor	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0010092	increased circulating magnesium level		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0010965	decreased compact bone volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517179
1553551	Casr	calcium-sensing receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20221103	MGI			
1553551	Casr	calcium-sensing receptor	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0013572	abnormal parathyroid gland chief cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:7493018
1553551	Casr	calcium-sensing receptor	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20200310	MGI			PMID:18765830
1553551	Casr	calcium-sensing receptor	gene	MP:0030129	tongue inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15347804
1553554	Cd274	CD274 antigen	gene	MP:0001790	abnormal immune system physiology		IEA		N	RGD:5509061	20200310	MGI			
1553554	Cd274	CD274 antigen	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25964334
1553554	Cd274	CD274 antigen	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15030776
1553554	Cd274	CD274 antigen	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16606670
1553554	Cd274	CD274 antigen	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19710456
1553554	Cd274	CD274 antigen	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:20639491
1553554	Cd274	CD274 antigen	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15249675
1553554	Cd274	CD274 antigen	gene	MP:0002738	hyperresponsive to tactile stimuli		IAGP		N	RGD:5509061	20200310	MGI			PMID:20051242
1553554	Cd274	CD274 antigen	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:16358363
1553554	Cd274	CD274 antigen	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:17182110
1553554	Cd274	CD274 antigen	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15030776
1553554	Cd274	CD274 antigen	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20250925	MGI			PMID:30382149
1553554	Cd274	CD274 antigen	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:17182110
1553554	Cd274	CD274 antigen	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18825752
1553554	Cd274	CD274 antigen	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20200310	MGI			PMID:16606670
1553554	Cd274	CD274 antigen	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20200310	MGI			PMID:17911591
1553554	Cd274	CD274 antigen	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15249675
1553554	Cd274	CD274 antigen	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18825752
1553554	Cd274	CD274 antigen	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20200310	MGI			PMID:16358363
1553554	Cd274	CD274 antigen	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200310	MGI			PMID:20051242
1553554	Cd274	CD274 antigen	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20200310	MGI			PMID:15030776
1553554	Cd274	CD274 antigen	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15030776
1553554	Cd274	CD274 antigen	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18490751
1553554	Cd274	CD274 antigen	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18490751
1553554	Cd274	CD274 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:15030776
1553554	Cd274	CD274 antigen	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19710456
1553554	Cd274	CD274 antigen	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:17182110
1553554	Cd274	CD274 antigen	gene	MP:0008087	decreased T helper 1 cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20639491
1553554	Cd274	CD274 antigen	gene	MP:0008088	abnormal T-helper 1 cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20639491
1553554	Cd274	CD274 antigen	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20639491
1553554	Cd274	CD274 antigen	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20051242
1553554	Cd274	CD274 antigen	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:16606670
1553554	Cd274	CD274 antigen	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:16606670
1553554	Cd274	CD274 antigen	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:16606670
1553554	Cd274	CD274 antigen	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20250925	MGI			PMID:30382149
1553554	Cd274	CD274 antigen	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:16606670
1553554	Cd274	CD274 antigen	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20051242
1553554	Cd274	CD274 antigen	gene	MP:0008896	increased IgG2c level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20639491
1553554	Cd274	CD274 antigen	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:20639491
1553554	Cd274	CD274 antigen	gene	MP:0010189	abnormal T follicular helper cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0010220	decreased T-helper 17 cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21061440
1553554	Cd274	CD274 antigen	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16027236
1553554	Cd274	CD274 antigen	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18490751
1553554	Cd274	CD274 antigen	gene	MP:0031023	decreased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:18490751
1553557	Sbk1	SH3-binding kinase 1	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1553557	Sbk1	SH3-binding kinase 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20200402	MGI			
1553557	Sbk1	SH3-binding kinase 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20250508	MGI			
1553557	Sbk1	SH3-binding kinase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553557	Sbk1	SH3-binding kinase 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20201231	MGI			
1553557	Sbk1	SH3-binding kinase 1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1553557	Sbk1	SH3-binding kinase 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12805213
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12805213
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20200310	MGI			PMID:19002527
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19002527
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12805213
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12805213
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12805213
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0003414	epidermal cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:12805213
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0009623	enlarged inguinal lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0009631	enlarged axillary lymph nodes		IAGP		N	RGD:5509061	20200310	MGI			PMID:22805570
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:12805213
1553559	Plcd1	phospholipase C, delta 1	gene	MP:0013378	increased sebocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:12805213
1553560	Tmprss11b	transmembrane protease, serine 11B	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20191031	MGI			PMID:31501243
1553561	Dhrs2	dehydrogenase/reductase member 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20201231	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20201022	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201022	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20241121	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20201022	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20210128	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20210902	MGI			PMID:33560420
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20191128	MGI			PMID:31479441
1553562	Bbs5	Bardet-Biedl syndrome 5	gene	MP:0020511	decreased dendritic spine length		IAGP		N	RGD:5509061	20191128	MGI			PMID:31479441
1553568	St3gal6	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1553568	St3gal6	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1553568	St3gal6	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1553568	St3gal6	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1553568	St3gal6	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1553568	St3gal6	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1553568	St3gal6	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700726
1553568	St3gal6	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:22700726
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922412
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20151112	MGI			
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368758
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922412
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383102
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0001765	abnormal ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368758
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383102
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0002829	abnormal juxtaglomerular apparatus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922412
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922412
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922412
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0003186	abnormal redox activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922412
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368758
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0004142	abnormal muscle tone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922412
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16361444
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922412
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0005634	decreased circulating sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922412
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21383102
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368758
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0010109	abnormal renal sodium reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0010128	hypovolemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0011299	abnormal macula densa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0011300	abnormal juxtaglomerular cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0011302	abnormal extraglomerular mesangial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0011442	abnormal renal sodium ion transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689096
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0014746	abnormal hippocampal mossy fiber innervation pattern		IAGP		N	RGD:5509061	20250911	MGI			PMID:16368758
1553569	Nr3c2	nuclear receptor subfamily 3, group C, member 2	gene	MP:0031232	increased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:9689096
1553572	Tmprss11d	transmembrane protease, serine 11d	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20200310	MGI			PMID:31501243
1553572	Tmprss11d	transmembrane protease, serine 11d	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:21853097
1553576	F11r	F11 receptor	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343392
1553576	F11r	F11 receptor	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809549
1553576	F11r	F11 receptor	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15343392
1553576	F11r	F11 receptor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16809549
1553577	Gsto2	glutathione S-transferase omega 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1553577	Gsto2	glutathione S-transferase omega 2	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20200402	MGI			
1553577	Gsto2	glutathione S-transferase omega 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20150108	MGI			
1553577	Gsto2	glutathione S-transferase omega 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0000445	short snout		IEA		N	RGD:5509061	20150827	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0000520	absent kidney		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19421194
1553585	Plxnd1	plexin D1	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19421194
1553585	Plxnd1	plexin D1	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1553585	Plxnd1	plexin D1	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0002276	abnormal lung interstitium morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20150827	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0002726	abnormal pulmonary vein morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210822
1553585	Plxnd1	plexin D1	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0004612	fusion of vertebral bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21505259
1553585	Plxnd1	plexin D1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0010406	common atrium		IEA		N	RGD:5509061	20150827	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0010413	complete atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20150827	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0010472	abnormal ascending aorta and coronary artery attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0010488	abnormal left subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0010565	absent fetal ductus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0011661	persistent truncus arteriosus type i		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0011662	persistent truncus arteriosus type ii		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0011681	atrium cyst		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0011682	renal glomerulus cyst		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20141003	MGI			
1553585	Plxnd1	plexin D1	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15239958
1553585	Plxnd1	plexin D1	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15550623
1553585	Plxnd1	plexin D1	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18992737
1553585	Plxnd1	plexin D1	gene	MP:0013975	abnormal coronary sinus connection		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0020330	increased capillary density		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0031152	subcutaneous hemorrhage		IAGP		N	RGD:5509061	20231109	MGI			PMID:34791216
1553585	Plxnd1	plexin D1	gene	MP:0031589	detached epicardium		IAGP		N	RGD:5509061	20240229	MGI			PMID:18992737
1553588	Notch4	notch 4	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991352
1553588	Notch4	notch 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24667410
1553588	Notch4	notch 4	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0004784	abnormal anterior cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553588	Notch4	notch 4	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24667410
1553588	Notch4	notch 4	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10837027
1553592	Zfp516	zinc finger protein 516	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25578880
1553592	Zfp516	zinc finger protein 516	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20200310	MGI			PMID:25578880
1553592	Zfp516	zinc finger protein 516	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25578880
1553592	Zfp516	zinc finger protein 516	gene	MP:0011170	abnormal brown fat cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25578880
1553592	Zfp516	zinc finger protein 516	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20200310	MGI			PMID:25578880
1553593	Otp	orthopedia homeobox	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481897
1553593	Otp	orthopedia homeobox	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0004164	abnormal neurohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0005448	abnormal energy homeostasis		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1553593	Otp	orthopedia homeobox	gene	MP:0008845	abnormal paraventricular hypothalamic nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0008846	abnormal supraoptic nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0009229	abnormal neurohypophysis median eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071765
1553593	Otp	orthopedia homeobox	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553593	Otp	orthopedia homeobox	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20200416	MGI			PMID:29107289
1553595	Tcf3	transcription factor 3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365147
1553595	Tcf3	transcription factor 3	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365147
1553595	Tcf3	transcription factor 3	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365147
1553595	Tcf3	transcription factor 3	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
1553595	Tcf3	transcription factor 3	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857655
1553595	Tcf3	transcription factor 3	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001124
1553595	Tcf3	transcription factor 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
1553595	Tcf3	transcription factor 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19822014
1553595	Tcf3	transcription factor 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19822014
1553595	Tcf3	transcription factor 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001124
1553595	Tcf3	transcription factor 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8649400
1553595	Tcf3	transcription factor 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19752184
1553595	Tcf3	transcription factor 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19822014
1553595	Tcf3	transcription factor 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442955
1553595	Tcf3	transcription factor 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18384878
1553595	Tcf3	transcription factor 3	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
1553595	Tcf3	transcription factor 3	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062079
1553595	Tcf3	transcription factor 3	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062079
1553595	Tcf3	transcription factor 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19822014
1553595	Tcf3	transcription factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062079
1553595	Tcf3	transcription factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19752184
1553595	Tcf3	transcription factor 3	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062079
1553595	Tcf3	transcription factor 3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937548
1553595	Tcf3	transcription factor 3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
1553595	Tcf3	transcription factor 3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093538
1553595	Tcf3	transcription factor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937548
1553595	Tcf3	transcription factor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17316599
1553595	Tcf3	transcription factor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22354994
1553595	Tcf3	transcription factor 3	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452521
1553595	Tcf3	transcription factor 3	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365147
1553595	Tcf3	transcription factor 3	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001125
1553595	Tcf3	transcription factor 3	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15078898
1553595	Tcf3	transcription factor 3	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001124
1553595	Tcf3	transcription factor 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
1553595	Tcf3	transcription factor 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
1553595	Tcf3	transcription factor 3	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001124
1553595	Tcf3	transcription factor 3	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
1553595	Tcf3	transcription factor 3	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001125
1553595	Tcf3	transcription factor 3	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093538
1553595	Tcf3	transcription factor 3	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195039
1553595	Tcf3	transcription factor 3	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062079
1553595	Tcf3	transcription factor 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001125
1553595	Tcf3	transcription factor 3	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452521
1553595	Tcf3	transcription factor 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001124
1553595	Tcf3	transcription factor 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001125
1553595	Tcf3	transcription factor 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442955
1553595	Tcf3	transcription factor 3	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062079
1553595	Tcf3	transcription factor 3	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937548
1553595	Tcf3	transcription factor 3	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442955
1553595	Tcf3	transcription factor 3	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18384878
1553595	Tcf3	transcription factor 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442955
1553595	Tcf3	transcription factor 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18384878
1553595	Tcf3	transcription factor 3	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18195039
1553595	Tcf3	transcription factor 3	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442955
1553595	Tcf3	transcription factor 3	gene	MP:0005432	abnormal pro-B cell morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452521
1553595	Tcf3	transcription factor 3	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365147
1553595	Tcf3	transcription factor 3	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:19752184
1553595	Tcf3	transcription factor 3	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093538
1553595	Tcf3	transcription factor 3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18093538
1553595	Tcf3	transcription factor 3	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11937548
1553595	Tcf3	transcription factor 3	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18384878
1553595	Tcf3	transcription factor 3	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365147
1553595	Tcf3	transcription factor 3	gene	MP:0008176	abnormal germinal center B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0008187	absent pro-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365147
1553595	Tcf3	transcription factor 3	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19752184
1553595	Tcf3	transcription factor 3	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8649400
1553595	Tcf3	transcription factor 3	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15078898
1553595	Tcf3	transcription factor 3	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19752184
1553595	Tcf3	transcription factor 3	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0008233	abnormal pro-B cell differentiation		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553595	Tcf3	transcription factor 3	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0008755	abnormal immunoglobulin V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001125
1553595	Tcf3	transcription factor 3	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1553595	Tcf3	transcription factor 3	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19822014
1553595	Tcf3	transcription factor 3	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001125
1553595	Tcf3	transcription factor 3	gene	MP:0008761	abnormal immunoglobulin light chain V-J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19752184
1553595	Tcf3	transcription factor 3	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452521
1553595	Tcf3	transcription factor 3	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452521
1553595	Tcf3	transcription factor 3	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452521
1553595	Tcf3	transcription factor 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062079
1553595	Tcf3	transcription factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16315099
1553595	Tcf3	transcription factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001124
1553595	Tcf3	transcription factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001125
1553595	Tcf3	transcription factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8649400
1553595	Tcf3	transcription factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9584174
1553595	Tcf3	transcription factor 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9372963
1553595	Tcf3	transcription factor 3	gene	MP:0014050	increased B cell acute lymphoblastic leukemia incidence		IAGP		N	RGD:5509061	20170314	MGI			PMID:26301816
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000188	abnormal circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314549
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736651
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559824
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8164737
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736651
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:24658838
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093877
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093877
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093877
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093877
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093877
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180111	MGI			PMID:21964024
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19084435
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002343	abnormal lymph node cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:8164737
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17562770
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8164737
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9820556
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559824
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314549
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093877
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0003699	abnormal female reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10639149
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919943
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0003865	lymph node inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736651
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314549
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10946317
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314549
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736651
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594834
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11801676
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24658838
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7972104
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:8164737
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7526382
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7972104
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8164737
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308121
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005580	periinsulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314549
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20231207	MGI			
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:15308121
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:17114464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9736651
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919943
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14557749
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559824
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11559824
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008573	increased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008635	increased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17562770
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008791	decreased NK cell degranulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:9314549
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0009022	abnormal brain meninges morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15061770
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116214
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919943
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0009791	increased susceptibility to viral infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093877
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093877
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16116214
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919943
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18563383
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0012330	decreased circulating fibrinogen level		IAGP		N	RGD:5509061	20200618	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12093877
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11559824
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23160464
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:7526382
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:8164737
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IEA		N	RGD:5509061	20200430	MGI			
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:9736651
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0020943	increased susceptibility to Flaviviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:15061770
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:15069016
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IEA		N	RGD:5509061	20200514	MGI			
1553597	Prf1	perforin 1 (pore forming protein)	gene	MP:0031052	lymph node necrosis		IAGP		N	RGD:5509061	20200618	MGI			PMID:15069016
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20240523	MGI			
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16630838
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16630838
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111215	MGI			
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0002330	abnormal bronchial provocation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059884
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0002498	abnormal acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564016
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0002733	abnormal thermal nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564016
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564016
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0003043	hypoalgesia		IEA		N	RGD:5509061	20111215	MGI			
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0003460	decreased fear-related response		IAGP		N	RGD:5509061	20181011	MGI			PMID:29795268
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0003663	abnormal thermosensation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16630838
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18499726
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059884
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:16564016
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0005407	hyperalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564016
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:16630838
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0008531	increased chemical nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:16564016
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19059884
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0010055	abnormal sensory neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18499726
1553598	Trpa1	transient receptor potential cation channel, subfamily A, member 1	gene	MP:0011968	decreased threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16630838
1553600	Colec12	collectin sub-family member 12	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1553600	Colec12	collectin sub-family member 12	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20241121	MGI			
1553600	Colec12	collectin sub-family member 12	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20200514	MGI			
1553600	Colec12	collectin sub-family member 12	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20241121	MGI			
1553600	Colec12	collectin sub-family member 12	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20241121	MGI			
1553600	Colec12	collectin sub-family member 12	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200514	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20201022	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20181227	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000493	rectal prolapse		IEA		N	RGD:5509061	20240208	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20240222	MGI			PMID:38198538
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20240222	MGI			PMID:38198538
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:38198538
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20240222	MGI			PMID:38198538
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20240222	MGI			PMID:38198538
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20181227	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20201022	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0030166	increased inner canthal distance		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553608	Rreb1	ras responsive element binding protein 1	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20221006	MGI			PMID:32938917
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0001499	abnormal kindling response		IAGP		N	RGD:5509061	20160204	MGI			PMID:26063919
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20160204	MGI			PMID:26063919
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20160204	MGI			PMID:26063919
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002637	small uterus		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20160204	MGI			PMID:26063919
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160204	MGI			PMID:26063919
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:26063919
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:26063919
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20210819	MGI			PMID:34184986
1553609	Fgf13	fibroblast growth factor 13	gene	MP:0031752	decreased inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20260813	MGI			PMID:26063919
1553611	Ngb	neuroglobin	gene	MP:0020475	delayed circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:22496809
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15140899
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15140899
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15140899
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15140899
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15140899
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0009974	decreased cerebral cortex pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0010012	ectopic cerebral cortex pyramidal cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0014551	impaired neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:17682066
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0014745	abnormal hippocampal mossy fiber infrapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:15140899
1553612	St8sia2	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	gene	MP:0014746	abnormal hippocampal mossy fiber innervation pattern		IAGP		N	RGD:5509061	20250911	MGI			PMID:15140899
1553613	Psmd6	proteasome (prosome, macropain) 26S subunit, non-ATPase, 6	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553616	Hcrtr2	hypocretin (orexin) receptor 2	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12797957
1553616	Hcrtr2	hypocretin (orexin) receptor 2	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377495
1553616	Hcrtr2	hypocretin (orexin) receptor 2	gene	MP:0004142	abnormal muscle tone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368172
1553616	Hcrtr2	hypocretin (orexin) receptor 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368172
1553616	Hcrtr2	hypocretin (orexin) receptor 2	gene	MP:0005279	narcolepsy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12797957
1553616	Hcrtr2	hypocretin (orexin) receptor 2	gene	MP:0005279	narcolepsy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368172
1553616	Hcrtr2	hypocretin (orexin) receptor 2	gene	MP:0009436	fragmentation of sleep/wake states		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368172
1553616	Hcrtr2	hypocretin (orexin) receptor 2	gene	MP:0012288	abnormal paradoxical sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12797957
1553616	Hcrtr2	hypocretin (orexin) receptor 2	gene	MP:0012289	abnormal non-rapid eye movement sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12797957
1553619	Ppp3cc	protein phosphatase 3, catalytic subunit, gamma isoform	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20160818	MGI			PMID:26429887
1553619	Ppp3cc	protein phosphatase 3, catalytic subunit, gamma isoform	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160818	MGI			PMID:26429887
1553619	Ppp3cc	protein phosphatase 3, catalytic subunit, gamma isoform	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20231207	MGI			
1553619	Ppp3cc	protein phosphatase 3, catalytic subunit, gamma isoform	gene	MP:0009282	decreased hyperactivated sperm motility		IAGP		N	RGD:5509061	20160818	MGI			PMID:26429887
1553619	Ppp3cc	protein phosphatase 3, catalytic subunit, gamma isoform	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20160818	MGI			PMID:26429887
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20231207	MGI			
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20231207	MGI			
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0004156	abnormal QT variability		IEA		N	RGD:5509061	20260402	MGI			
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20231207	MGI			
1553620	Eprs1	glutamyl-prolyl-tRNA synthetase 1	gene	MP:0014173	increased fatty acid beta-oxidation		IAGP		N	RGD:5509061	20180531	MGI			PMID:28178239
1553621	Timmdc1	translocase of inner mitochondrial membrane domain containing 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201022	MGI			
1553621	Timmdc1	translocase of inner mitochondrial membrane domain containing 1	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1553621	Timmdc1	translocase of inner mitochondrial membrane domain containing 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1553621	Timmdc1	translocase of inner mitochondrial membrane domain containing 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1553621	Timmdc1	translocase of inner mitochondrial membrane domain containing 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20141003	MGI			
1553621	Timmdc1	translocase of inner mitochondrial membrane domain containing 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1553621	Timmdc1	translocase of inner mitochondrial membrane domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1553625	Mak16	MAK16 homolog	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1553625	Mak16	MAK16 homolog	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553625	Mak16	MAK16 homolog	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1553626	Als2cl	ALS2 C-terminal like	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1553628	Klhl10	kelch-like 10	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136734
1553628	Klhl10	kelch-like 10	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136734
1553628	Klhl10	kelch-like 10	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136734
1553628	Klhl10	kelch-like 10	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136734
1553628	Klhl10	kelch-like 10	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136734
1553628	Klhl10	kelch-like 10	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136734
1553628	Klhl10	kelch-like 10	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15136734
1553630	Gpatch4	G patch domain containing 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1553630	Gpatch4	G patch domain containing 4	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20240523	MGI			
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16234353
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20200310	MGI			PMID:16234353
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19494112
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17297474
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:16234353
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16234353
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:17297474
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16234353
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16234353
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20200310	MGI			PMID:16234353
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0009734	abnormal prostate gland duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19494112
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0009736	abnormal prostate gland branching morphogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19494112
1553632	Klf6	Kruppel-like transcription factor 6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16234353
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571152
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15629699
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19846708
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451647
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451647
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0003463	abnormal single cell response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571152
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250911	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451647
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:19571152
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17553423
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0008726	increased heart left atrium size		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20220519	MGI			
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20231109	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0010613	abnormal mitral valve annulus morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20190215	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0020374	abnormal nocifensive behavior		IAGP		N	RGD:5509061	20210204	MGI			PMID:32084332
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0020955	increased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20210204	MGI			PMID:32084332
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:30339496
1553636	Mrgprd	MAS-related GPR, member D	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231109	MGI			PMID:30339496
1553638	Pdxk	pyridoxal (pyridoxine, vitamin B6) kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553639	Clec3b	C-type lectin domain family 3, member b	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11604516
1553639	Clec3b	C-type lectin domain family 3, member b	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11604516
1553639	Clec3b	C-type lectin domain family 3, member b	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11604516
1553639	Clec3b	C-type lectin domain family 3, member b	gene	MP:0005227	abnormal vertebral body development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11604516
1553639	Clec3b	C-type lectin domain family 3, member b	gene	MP:0005229	abnormal intervertebral disk development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11604516
1553639	Clec3b	C-type lectin domain family 3, member b	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11604516
1553639	Clec3b	C-type lectin domain family 3, member b	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1553639	Clec3b	C-type lectin domain family 3, member b	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:11604516
1553642	Zfp697	zinc finger protein 697	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20250515	MGI			PMID:39141348
1553642	Zfp697	zinc finger protein 697	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20250515	MGI			PMID:39141348
1553642	Zfp697	zinc finger protein 697	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20240523	MGI			
1553642	Zfp697	zinc finger protein 697	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20250515	MGI			PMID:39141348
1553642	Zfp697	zinc finger protein 697	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20250508	MGI			
1553642	Zfp697	zinc finger protein 697	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20250515	MGI			PMID:39141348
1553642	Zfp697	zinc finger protein 697	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20250515	MGI			PMID:39141348
1553642	Zfp697	zinc finger protein 697	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20250515	MGI			PMID:39141348
1553644	Vwf	Von Willebrand factor	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689113
1553644	Vwf	Von Willebrand factor	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18688020
1553644	Vwf	Von Willebrand factor	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10930441
1553644	Vwf	Von Willebrand factor	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689113
1553644	Vwf	Von Willebrand factor	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20201210	MGI			PMID:30565388
1553644	Vwf	Von Willebrand factor	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20181220	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182208
1553644	Vwf	Von Willebrand factor	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20181220	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0003292	melena		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689113
1553644	Vwf	Von Willebrand factor	gene	MP:0004720	abnormal platelet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083848
1553644	Vwf	Von Willebrand factor	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18688020
1553644	Vwf	Von Willebrand factor	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20181220	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20181220	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0005341	decreased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520791
1553644	Vwf	Von Willebrand factor	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689113
1553644	Vwf	Von Willebrand factor	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20181220	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20201210	MGI			PMID:30565388
1553644	Vwf	Von Willebrand factor	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20181220	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084279
1553644	Vwf	Von Willebrand factor	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:9689113
1553644	Vwf	Von Willebrand factor	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20150611	MGI			PMID:25293780
1553644	Vwf	Von Willebrand factor	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20181220	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20201210	MGI			PMID:30565388
1553644	Vwf	Von Willebrand factor	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182208
1553644	Vwf	Von Willebrand factor	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084279
1553644	Vwf	Von Willebrand factor	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083848
1553644	Vwf	Von Willebrand factor	gene	MP:0009548	abnormal platelet aggregation		IAGP		N	RGD:5509061	20181220	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20181220	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18083848
1553644	Vwf	Von Willebrand factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10930441
1553644	Vwf	Von Willebrand factor	gene	MP:0012359	increased partial thromboplastin time		IAGP		N	RGD:5509061	20201001	MGI			PMID:9689113
1553644	Vwf	Von Willebrand factor	gene	MP:0020215	impaired blood coagulation		IAGP		N	RGD:5509061	20150611	MGI			PMID:25293780
1553644	Vwf	Von Willebrand factor	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:11520791
1553644	Vwf	Von Willebrand factor	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:27212476
1553644	Vwf	Von Willebrand factor	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:10930441
1553644	Vwf	Von Willebrand factor	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:18083848
1553644	Vwf	Von Willebrand factor	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:30565388
1553644	Vwf	Von Willebrand factor	gene	MP:0031384	impaired blood-brain barrier function		IAGP		N	RGD:5509061	20220407	MGI			PMID:18688020
1553646	Ndufa11	NADH:ubiquinone oxidoreductase subunit A11	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20241010	MGI			
1553646	Ndufa11	NADH:ubiquinone oxidoreductase subunit A11	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20241010	MGI			
1553646	Ndufa11	NADH:ubiquinone oxidoreductase subunit A11	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20241010	MGI			
1553646	Ndufa11	NADH:ubiquinone oxidoreductase subunit A11	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20241010	MGI			
1553646	Ndufa11	NADH:ubiquinone oxidoreductase subunit A11	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1553646	Ndufa11	NADH:ubiquinone oxidoreductase subunit A11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1553646	Ndufa11	NADH:ubiquinone oxidoreductase subunit A11	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20241010	MGI			
1553646	Ndufa11	NADH:ubiquinone oxidoreductase subunit A11	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1553653	Me3	malic enzyme 3, NADP(+)-dependent, mitochondrial	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1553653	Me3	malic enzyme 3, NADP(+)-dependent, mitochondrial	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20250508	MGI			
1553653	Me3	malic enzyme 3, NADP(+)-dependent, mitochondrial	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1553653	Me3	malic enzyme 3, NADP(+)-dependent, mitochondrial	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1553653	Me3	malic enzyme 3, NADP(+)-dependent, mitochondrial	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000071	axial skeleton hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000071	axial skeleton hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000071	axial skeleton hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000071	axial skeleton hypoplasia		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20200310	MGI			
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004340	short scapula		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18695242
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23479625
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201029	MGI			PMID:30865697
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0030245	round head		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553656	Bpnt2	3'(2'), 5'-bisphosphate nucleotidase 2	gene	MP:0030837	abnormal knee joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18539921
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000172	abnormal bone marrow cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:19188446
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:8098731
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:9256469
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11067886
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20180719	MGI			PMID:8810244
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11602620
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11937578
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:7679955
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:9256469
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:10384121
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11290790
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:9256469
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:10384121
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:19587020
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20210527	MGI			PMID:24983315
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11602620
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11602620
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:11937578
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0004919	abnormal positive T cell selection		IAGP		N	RGD:5509061	20180719	MGI			PMID:10843678
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23267015
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:9551884
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20180719	MGI			PMID:10384121
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20180719	MGI			PMID:11290790
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20180719	MGI			PMID:12646641
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20180719	MGI			PMID:15034026
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20180719	MGI			PMID:7553002
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20180719	MGI			PMID:8098731
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005041	abnormal antigen presentation via MHC class II		IAGP		N	RGD:5509061	20180719	MGI			PMID:8977190
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20180719	MGI			PMID:7553002
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20180719	MGI			PMID:8098731
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20180719	MGI			PMID:8294875
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20180719	MGI			PMID:8977190
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20180719	MGI			PMID:9551884
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005043	defective assembly of class II molecules		IAGP		N	RGD:5509061	20180719	MGI			PMID:7553002
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005043	defective assembly of class II molecules		IAGP		N	RGD:5509061	20180719	MGI			PMID:8098731
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005043	defective assembly of class II molecules		IAGP		N	RGD:5509061	20180719	MGI			PMID:8977190
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:16484589
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:8810244
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:10384121
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11602620
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:7553002
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20180719	MGI			PMID:8098731
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:7553002
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11937578
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20180719	MGI			PMID:11937578
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:12634786
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:10384121
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:11290790
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:15034026
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7553002
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7679955
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8098731
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:8810244
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:9256469
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:9551884
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:7679955
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:9256469
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23267015
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:23267013
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:10384121
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11602620
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20180719	MGI			PMID:11602620
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20180719	MGI			PMID:11067886
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0013657	abnormal blood cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0013705	decreased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:19966810
1553657	Cd74	CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated)	gene	MP:0031217	increased susceptibility to myocardial ischemic injury		IAGP		N	RGD:5509061	20210527	MGI			PMID:24983315
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239462
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239462
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0001603	failure of myelopoiesis		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239462
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239462
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14963485
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239462
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239462
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239462
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239462
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14963485
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14963485
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14963485
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14963485
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0013741	absent thymus corticomedullary boundary		IAGP		N	RGD:5509061	20150430	MGI			PMID:11239462
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0013776	bone marrow failure		IAGP		N	RGD:5509061	20151126	MGI			PMID:25965569
1553658	Srsf2	serine and arginine-rich splicing factor 2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:14963485
1553660	Zer1	zyg-11 related, cell cycle regulator	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1553660	Zer1	zyg-11 related, cell cycle regulator	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1553660	Zer1	zyg-11 related, cell cycle regulator	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1553662	Pck2	phosphoenolpyruvate carboxykinase 2 (mitochondrial)	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20220519	MGI			
1553662	Pck2	phosphoenolpyruvate carboxykinase 2 (mitochondrial)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1553662	Pck2	phosphoenolpyruvate carboxykinase 2 (mitochondrial)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1553662	Pck2	phosphoenolpyruvate carboxykinase 2 (mitochondrial)	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20210826	MGI			
1553662	Pck2	phosphoenolpyruvate carboxykinase 2 (mitochondrial)	gene	MP:0004930	small epididymis		IEA		N	RGD:5509061	20220519	MGI			
1553664	Ift140	intraflagellar transport 140	gene	MP:0000075	absent neurocranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000080	abnormal exoccipital bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20200310	MGI			
1553664	Ift140	intraflagellar transport 140	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20200310	MGI			PMID:23469164
1553664	Ift140	intraflagellar transport 140	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23469164
1553664	Ift140	intraflagellar transport 140	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:23469164
1553664	Ift140	intraflagellar transport 140	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0000690	absent spleen		IEA		N	RGD:5509061	20200310	MGI			
1553664	Ift140	intraflagellar transport 140	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:23469164
1553664	Ift140	intraflagellar transport 140	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23469164
1553664	Ift140	intraflagellar transport 140	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0002633	persistent truncus arteriosus		IEA		N	RGD:5509061	20200310	MGI			
1553664	Ift140	intraflagellar transport 140	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20200310	MGI			PMID:23469164
1553664	Ift140	intraflagellar transport 140	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0003178	left pulmonary isomerism		IEA		N	RGD:5509061	20200310	MGI			
1553664	Ift140	intraflagellar transport 140	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0004113	abnormal aortic arch morphology		IEA		N	RGD:5509061	20200310	MGI			
1553664	Ift140	intraflagellar transport 140	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20200310	MGI			
1553664	Ift140	intraflagellar transport 140	gene	MP:0004458	absent alisphenoid bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0004476	absent palatine bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0008149	abnormal costovertebral joint morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0009837	abnormal sperm end piece morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0009877	exostosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20200310	MGI			
1553664	Ift140	intraflagellar transport 140	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23469164
1553664	Ift140	intraflagellar transport 140	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0013167	abnormal hindlimb bud morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0013203	abnormal primary cilium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:23469164
1553664	Ift140	intraflagellar transport 140	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0020383	decreased kidney epithelial cell primary cilium length		IAGP		N	RGD:5509061	20200310	MGI			PMID:22282595
1553664	Ift140	intraflagellar transport 140	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220210	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0030385	decreased facial bone number		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0030386	facial bone hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:24009529
1553664	Ift140	intraflagellar transport 140	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:29236364
1553664	Ift140	intraflagellar transport 140	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220317	MGI			PMID:29236364
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:29928881
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0002204	abnormal synaptic neurotransmitter level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29928881
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0003242	loss of basal ganglia neurons		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IEA		N	RGD:5509061	20201231	MGI			
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0010177	acanthocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15686477
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0014465	abnormal sperm mitochondrial morphology		IAGP		N	RGD:5509061	20240613	MGI			PMID:29928881
1553666	Vps13a	vacuolar protein sorting 13A	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:15686477
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20201022	MGI			
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20230601	MGI			
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20260402	MGI			
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20201022	MGI			
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0013519	decreased CD4-positive NK T cell number		IEA		N	RGD:5509061	20210128	MGI			
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0013769	increased marginal zone precursor B cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553668	Pdia6	protein disulfide isomerase associated 6	gene	MP:0013893	decreased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20201001	MGI			PMID:31985756
1553672	Atp13a4	ATPase type 13A4	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1553672	Atp13a4	ATPase type 13A4	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20240523	MGI			
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918574
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20152175
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20703245
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20703245
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20260402	MGI			
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15458925
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260585
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20703245
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391252
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17623652
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757438
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:17623652
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20703245
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992256
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20703245
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12391252
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0002733	abnormal thermal nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:11433347
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17640968
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12511586
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15458925
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0005085	abnormal gallbladder physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431214
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:17640968
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17992256
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16691196
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156206
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11859856
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0006060	increased cerebral infarct size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15647743
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12759239
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0008636	decreased circulating interleukin-18 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16260585
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:14576054
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12511586
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17304351
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:12511586
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757438
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757438
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18757438
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918574
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20703245
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9918574
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22952456
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16434493
1553673	F2rl1	F2R like trypsin receptor 1	gene	MP:0020332	impaired leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:11086091
1553676	Tspan17	tetraspanin 17	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1553676	Tspan17	tetraspanin 17	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0000497	abnormal small intestine placement		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20180201	MGI			PMID:28931820
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20180201	MGI			PMID:28931820
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0002928	abnormal bile duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:28931820
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0003826	abnormal Mullerian duct morphology		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:28931820
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20180201	MGI			PMID:28931820
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20180201	MGI			PMID:28931820
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20210930	MGI			PMID:31087039
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0010439	abnormal hepatic vein morphology		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0011130	absent tertiary ovarian follicles		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0013507	increased ovary apoptosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0014003	additional anastomosis between intracranial vertebral arteries		IEA		N	RGD:5509061	20170504	MGI			
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553679	Tent5c	terminal nucleotidyltransferase 5C	gene	MP:0031474	increased female germ cell apoptosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20180111	MGI			PMID:28204537
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0005563	abnormal hemoglobin content		IAGP		N	RGD:5509061	20180111	MGI			PMID:28204537
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20160804	MGI			
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160804	MGI			
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0012552	lactic acidosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1553681	Sdhc	succinate dehydrogenase complex, subunit C, integral membrane protein	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:31469588
1553682	Paqr5	progestin and adipoQ receptor family member V	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20241121	MGI			
1553682	Paqr5	progestin and adipoQ receptor family member V	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1553682	Paqr5	progestin and adipoQ receptor family member V	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20240523	MGI			
1553682	Paqr5	progestin and adipoQ receptor family member V	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20240523	MGI			
1553682	Paqr5	progestin and adipoQ receptor family member V	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20240523	MGI			
1553683	Krt2	keratin 2	gene	MP:0000575	increased foot pad pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1553683	Krt2	keratin 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210805	MGI			
1553683	Krt2	keratin 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210805	MGI			
1553683	Krt2	keratin 2	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1553683	Krt2	keratin 2	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1553683	Krt2	keratin 2	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0001233	abnormal epidermis suprabasal layer morphology		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1553683	Krt2	keratin 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210805	MGI			
1553683	Krt2	keratin 2	gene	MP:0002656	abnormal keratinocyte differentiation		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210805	MGI			
1553683	Krt2	keratin 2	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20210805	MGI			
1553683	Krt2	keratin 2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0009599	thick epidermis stratum granulosum		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0009600	hypergranulosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20231207	MGI			
1553683	Krt2	keratin 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210805	MGI			
1553683	Krt2	keratin 2	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1553683	Krt2	keratin 2	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12533510
1553683	Krt2	keratin 2	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20161027	MGI			PMID:24751727
1553683	Krt2	keratin 2	gene	MP:0030605	abnormal corneocyte morphology		IAGP		N	RGD:5509061	20180628	MGI			PMID:24751727
1553684	Gpatch3	G patch domain containing 3	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1553684	Gpatch3	G patch domain containing 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20241121	MGI			
1553684	Gpatch3	G patch domain containing 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1553684	Gpatch3	G patch domain containing 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1553684	Gpatch3	G patch domain containing 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210826	MGI			
1553684	Gpatch3	G patch domain containing 3	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20241121	MGI			
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510570
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510570
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510570
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510570
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510570
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510570
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510570
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15924147
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15924147
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15924147
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20250508	MGI			
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15924147
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15924147
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510570
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15924147
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:15924147
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19729480
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510570
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12874803
1553686	Hmga1	high mobility group AT-hook 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1553690	Fibcd1	fibrinogen C domain containing 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20240808	MGI			PMID:34937773
1553690	Fibcd1	fibrinogen C domain containing 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20240808	MGI			PMID:34937773
1553690	Fibcd1	fibrinogen C domain containing 1	gene	MP:0005398	decreased susceptibility to fungal infection		IAGP		N	RGD:5509061	20240808	MGI			PMID:34937773
1553690	Fibcd1	fibrinogen C domain containing 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20260212	MGI			PMID:34937773
1553690	Fibcd1	fibrinogen C domain containing 1	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20240808	MGI			PMID:34937773
1553690	Fibcd1	fibrinogen C domain containing 1	gene	MP:0009786	decreased susceptibility to infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240808	MGI			PMID:34937773
1553690	Fibcd1	fibrinogen C domain containing 1	gene	MP:0014433	increased cytokine level		IAGP		N	RGD:5509061	20240808	MGI			PMID:34937773
1553690	Fibcd1	fibrinogen C domain containing 1	gene	MP:0014434	decreased cytokine level		IAGP		N	RGD:5509061	20240808	MGI			PMID:34937773
1553692	Snai1	snail family zinc finger 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689706
1553692	Snai1	snail family zinc finger 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397867
1553692	Snai1	snail family zinc finger 1	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689706
1553692	Snai1	snail family zinc finger 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689706
1553692	Snai1	snail family zinc finger 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397867
1553692	Snai1	snail family zinc finger 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188491
1553692	Snai1	snail family zinc finger 1	gene	MP:0003227	abnormal vascular branching morphogenesis		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0003891	increased allantois apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689706
1553692	Snai1	snail family zinc finger 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689706
1553692	Snai1	snail family zinc finger 1	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19188491
1553692	Snai1	snail family zinc finger 1	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689706
1553692	Snai1	snail family zinc finger 1	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0009889	persistence of medial edge epithelium during palatal shelf fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397867
1553692	Snai1	snail family zinc finger 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689706
1553692	Snai1	snail family zinc finger 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16801545
1553692	Snai1	snail family zinc finger 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20150903	MGI			PMID:24894949
1553692	Snai1	snail family zinc finger 1	gene	MP:0030280	short parietal bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:17376812
1553692	Snai1	snail family zinc finger 1	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:17376812
1553693	Scaf8	SR-related CTD-associated factor 8	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1553693	Scaf8	SR-related CTD-associated factor 8	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1553693	Scaf8	SR-related CTD-associated factor 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1553694	Cxxc5	CXXC finger 5	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20240314	MGI			PMID:35390758
1553694	Cxxc5	CXXC finger 5	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0008159	increased diameter of fibula		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0008162	increased diameter of tibia		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0008957	abnormal placenta junctional zone morphology		IAGP		N	RGD:5509061	20240314	MGI			PMID:35390758
1553694	Cxxc5	CXXC finger 5	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0011504	abnormal limb long bone morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0011519	abnormal placenta labyrinth size		IAGP		N	RGD:5509061	20240314	MGI			PMID:35390758
1553694	Cxxc5	CXXC finger 5	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0013149	macrodactyly		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20160225	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:25633194
1553694	Cxxc5	CXXC finger 5	gene	MP:0030487	abnormal osteocyte dendritic process morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:25633194
1553696	Pan2	PAN2 poly(A) specific ribonuclease subunit	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1553696	Pan2	PAN2 poly(A) specific ribonuclease subunit	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1553696	Pan2	PAN2 poly(A) specific ribonuclease subunit	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141003	MGI			
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832057
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20200310	MGI			PMID:14627648
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832057
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:14627648
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000853	absent cerebellar foliation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832057
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:24802945
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:15992381
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23064382
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24802945
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20200310	MGI			PMID:15992381
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20200310	MGI			PMID:24725413
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001899	absent long-term depression		IAGP		N	RGD:5509061	20200310	MGI			PMID:24802945
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20200310	MGI			PMID:24802945
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20200310	MGI			PMID:16407116
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832057
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:14627648
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002883	chromatolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:24725413
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20200310	MGI			PMID:24725413
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20200310	MGI			PMID:23064382
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0003927	increased cellular glucose import		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832057
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0008440	abnormal subplate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832057
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0009718	absent Purkinje cell layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832057
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0009938	abnormal hippocampus granule cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15992381
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15992381
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832057
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:11517264
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0011624	abnormal sensitization to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:20832057
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0012318	slow extinction of fear memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:24725413
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9010203
1553698	Cdk5r1	cyclin dependent kinase 5, regulatory subunit 1	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:14627648
1553700	Ctnna1	catenin alpha 1	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0000448	pointed snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0001230	epidermal desquamation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706703
1553700	Ctnna1	catenin alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706703
1553700	Ctnna1	catenin alpha 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023354
1553700	Ctnna1	catenin alpha 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023354
1553700	Ctnna1	catenin alpha 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1553700	Ctnna1	catenin alpha 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0002655	abnormal keratinocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023354
1553700	Ctnna1	catenin alpha 1	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20151203	MGI			PMID:26142281
1553700	Ctnna1	catenin alpha 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22421363
1553700	Ctnna1	catenin alpha 1	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21924256
1553700	Ctnna1	catenin alpha 1	gene	MP:0003420	delayed intramembranous bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:21924256
1553700	Ctnna1	catenin alpha 1	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706703
1553700	Ctnna1	catenin alpha 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706703
1553700	Ctnna1	catenin alpha 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706703
1553700	Ctnna1	catenin alpha 1	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023354
1553700	Ctnna1	catenin alpha 1	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18809908
1553700	Ctnna1	catenin alpha 1	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706703
1553700	Ctnna1	catenin alpha 1	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0009715	thick epidermis stratum basale		IAGP		N	RGD:5509061	20141003	MGI			PMID:11239416
1553700	Ctnna1	catenin alpha 1	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0010172	abnormal mammary gland epithelium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14706703
1553700	Ctnna1	catenin alpha 1	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16543460
1553700	Ctnna1	catenin alpha 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553700	Ctnna1	catenin alpha 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9023354
1553700	Ctnna1	catenin alpha 1	gene	MP:0012040	abnormal c-wave shape		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0012671	retina spots		IAGP		N	RGD:5509061	20161222	MGI			PMID:26691986
1553700	Ctnna1	catenin alpha 1	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:14706703
1553700	Ctnna1	catenin alpha 1	gene	MP:0031384	impaired blood-brain barrier function		IAGP		N	RGD:5509061	20230511	MGI			PMID:33497368
1553706	Gcnt3	glucosaminyl (N-acetyl) transferase 3, mucin type	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1553706	Gcnt3	glucosaminyl (N-acetyl) transferase 3, mucin type	gene	MP:0001666	abnormal intestinal absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1553706	Gcnt3	glucosaminyl (N-acetyl) transferase 3, mucin type	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1553706	Gcnt3	glucosaminyl (N-acetyl) transferase 3, mucin type	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1553706	Gcnt3	glucosaminyl (N-acetyl) transferase 3, mucin type	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1553706	Gcnt3	glucosaminyl (N-acetyl) transferase 3, mucin type	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1553706	Gcnt3	glucosaminyl (N-acetyl) transferase 3, mucin type	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1553706	Gcnt3	glucosaminyl (N-acetyl) transferase 3, mucin type	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1553706	Gcnt3	glucosaminyl (N-acetyl) transferase 3, mucin type	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1553707	Prpf38a	PRP38 pre-mRNA processing factor 38 (yeast) domain containing A	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1553707	Prpf38a	PRP38 pre-mRNA processing factor 38 (yeast) domain containing A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1553712	Mettl15	methyltransferase like 15	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20220922	MGI			PMID:35682734
1553712	Mettl15	methyltransferase like 15	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20220922	MGI			PMID:35682734
1553712	Mettl15	methyltransferase like 15	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20220922	MGI			PMID:35682734
1553712	Mettl15	methyltransferase like 15	gene	MP:0012315	impaired learning		IAGP		N	RGD:5509061	20220922	MGI			PMID:35682734
1553712	Mettl15	methyltransferase like 15	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20220922	MGI			PMID:35682734
1553716	Ankrd24	ankyrin repeat domain 24	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1553716	Ankrd24	ankyrin repeat domain 24	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1553718	Tox4	TOX high mobility group box family member 4	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1553718	Tox4	TOX high mobility group box family member 4	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1553718	Tox4	TOX high mobility group box family member 4	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1553718	Tox4	TOX high mobility group box family member 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553719	St6galnac3	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20200310	MGI			
1553719	St6galnac3	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20240523	MGI			
1553719	St6galnac3	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20240523	MGI			
1553719	St6galnac3	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20231102	MGI			PMID:37386100
1553719	St6galnac3	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1553719	St6galnac3	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	gene	MP:0031051	lymph node hemorrhage		IAGP		N	RGD:5509061	20231102	MGI			PMID:37386100
1553720	Aimp1	aminoacyl tRNA synthetase complex-interacting multifunctional protein 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1553720	Aimp1	aminoacyl tRNA synthetase complex-interacting multifunctional protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1553720	Aimp1	aminoacyl tRNA synthetase complex-interacting multifunctional protein 1	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15681823
1553720	Aimp1	aminoacyl tRNA synthetase complex-interacting multifunctional protein 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1553720	Aimp1	aminoacyl tRNA synthetase complex-interacting multifunctional protein 1	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15681823
1553720	Aimp1	aminoacyl tRNA synthetase complex-interacting multifunctional protein 1	gene	MP:0003642	absent seminal vesicle		IEA		N	RGD:5509061	20220519	MGI			
1553720	Aimp1	aminoacyl tRNA synthetase complex-interacting multifunctional protein 1	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20220519	MGI			
1553720	Aimp1	aminoacyl tRNA synthetase complex-interacting multifunctional protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20190502	MGI			
1553721	Serinc2	serine incorporator 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20231207	MGI			
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20150108	MGI			
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20201231	MGI			
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553723	Ralb	Ras like proto-oncogene B	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23063435
1553724	Ankrd16	ankyrin repeat domain 16	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:29769718
1553724	Ankrd16	ankyrin repeat domain 16	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:29769718
1553724	Ankrd16	ankyrin repeat domain 16	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:29769718
1553724	Ankrd16	ankyrin repeat domain 16	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:29769718
1553724	Ankrd16	ankyrin repeat domain 16	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:29769718
1553724	Ankrd16	ankyrin repeat domain 16	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29769718
1553726	Tars2	threonyl-tRNA synthetase 2, mitochondrial (putative)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1553726	Tars2	threonyl-tRNA synthetase 2, mitochondrial (putative)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553726	Tars2	threonyl-tRNA synthetase 2, mitochondrial (putative)	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1553728	Zcchc4	zinc finger, CCHC domain containing 4	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20250508	MGI			
1553728	Zcchc4	zinc finger, CCHC domain containing 4	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20250508	MGI			
1553731	Zfp574	zinc finger protein 574	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0002811	macrocytic anemia		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0011995	decreased leukemia incidence		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553731	Zfp574	zinc finger protein 574	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20250109	MGI			PMID:39047044
1553733	Aldh18a1	aldehyde dehydrogenase 18 family, member A1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1553733	Aldh18a1	aldehyde dehydrogenase 18 family, member A1	gene	MP:0009932	skin fibrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1553733	Aldh18a1	aldehyde dehydrogenase 18 family, member A1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1553733	Aldh18a1	aldehyde dehydrogenase 18 family, member A1	gene	MP:0011156	abnormal hypodermis fat layer morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25340873
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20230216	MGI			PMID:32258033
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20230216	MGI			PMID:32258033
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20230216	MGI			PMID:32258033
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:26416744
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20230216	MGI			PMID:32258033
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20230216	MGI			PMID:32258033
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20230216	MGI			PMID:32258033
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230216	MGI			PMID:32258033
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20230216	MGI			PMID:32258033
1553734	Ctnnal1	catenin alpha like 1	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20230216	MGI			PMID:32258033
1553737	Cuta	cutA divalent cation tolerance homolog	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1553737	Cuta	cutA divalent cation tolerance homolog	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1553737	Cuta	cutA divalent cation tolerance homolog	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1553737	Cuta	cutA divalent cation tolerance homolog	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1553737	Cuta	cutA divalent cation tolerance homolog	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1553737	Cuta	cutA divalent cation tolerance homolog	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1553738	Kif13b	kinesin family member 13B	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20150122	MGI			PMID:24469637
1553738	Kif13b	kinesin family member 13B	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1553738	Kif13b	kinesin family member 13B	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20200402	MGI			
1553738	Kif13b	kinesin family member 13B	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1553738	Kif13b	kinesin family member 13B	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20150122	MGI			PMID:24469637
1553738	Kif13b	kinesin family member 13B	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1553738	Kif13b	kinesin family member 13B	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1553738	Kif13b	kinesin family member 13B	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20150122	MGI			PMID:24469637
1553738	Kif13b	kinesin family member 13B	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1553738	Kif13b	kinesin family member 13B	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1553738	Kif13b	kinesin family member 13B	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1553738	Kif13b	kinesin family member 13B	gene	MP:0012329	increased circulating factor VIII level		IAGP		N	RGD:5509061	20150122	MGI			PMID:24469637
1553738	Kif13b	kinesin family member 13B	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31487503
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0000495	abnormal colon morphology		IEA		N	RGD:5509061	20210128	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20210520	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0000948	nonconvulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18215623
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325226
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325226
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210520	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20200514	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18215623
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18674745
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18674745
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18215623
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325226
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0003444	abnormal neurotransmitter uptake		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278042
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004396	decreased cochlear inner hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18674745
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004416	absent cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18674745
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004433	abnormal cochlear inner hair cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18674745
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004495	decreased synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:18215623
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004562	abnormal inner hair cell synaptic ribbon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18215623
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004562	abnormal inner hair cell synaptic ribbon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18674745
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004633	abnormal cochlear IHC efferent innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18674745
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18674745
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18215623
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004836	abnormal synaptic acetylcholine release		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278042
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210520	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18215623
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200514	MGI			
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0009253	abnormal sympathetic neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23325226
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278042
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0009754	enhanced behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278042
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18215623
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18674745
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0014620	abnormal interictal brain wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:18215623
1553740	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:18278042
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20230601	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210128	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000603	pale liver		IEA		N	RGD:5509061	20230601	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20230601	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210128	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20220519	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0010082	sternebra fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0010146	umbilical hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0010902	abnormal pulmonary alveolar sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206015
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553742	Col27a1	collagen, type XXVII, alpha 1	gene	MP:0030273	mandibular retrognathia		IAGP		N	RGD:5509061	20171026	MGI			PMID:22206015
1553743	Zfp24	zinc finger protein 24	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080941
1553743	Zfp24	zinc finger protein 24	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080941
1553743	Zfp24	zinc finger protein 24	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080941
1553743	Zfp24	zinc finger protein 24	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080941
1553743	Zfp24	zinc finger protein 24	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080941
1553743	Zfp24	zinc finger protein 24	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080941
1553743	Zfp24	zinc finger protein 24	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080941
1553743	Zfp24	zinc finger protein 24	gene	MP:0004264	abnormal extraembryonic tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064688
1553743	Zfp24	zinc finger protein 24	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064688
1553743	Zfp24	zinc finger protein 24	gene	MP:0008027	abnormal spinal cord white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080941
1553743	Zfp24	zinc finger protein 24	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080941
1553743	Zfp24	zinc finger protein 24	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064688
1553743	Zfp24	zinc finger protein 24	gene	MP:0011731	decreased myelin sheath thickness		IEA		N	RGD:5509061	20141003	MGI			
1553743	Zfp24	zinc finger protein 24	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20141003	MGI			
1553743	Zfp24	zinc finger protein 24	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17064688
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17468400
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372253
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000276	heart right ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389319
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17468400
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000293	absent myocardial trabeculae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000484	abnormal pulmonary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22408025
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001725	abnormal umbilical cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372253
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389319
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002624	abnormal tricuspid valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372253
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002745	abnormal atrioventricular valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17468400
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372253
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372253
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22408025
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0003410	abnormal artery development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0003828	pulmonary edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17468400
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0003974	abnormal endocardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22408025
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004225	patent cardiac foramen ovale		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389319
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22408025
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20250911	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17468400
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22408025
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17468400
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006044	tricuspid valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006045	mitral valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006046	atrioventricular valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006123	tricuspid valve atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006123	tricuspid valve atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389319
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006123	tricuspid valve atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006124	tricuspid valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006124	tricuspid valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389319
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006124	tricuspid valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006128	pulmonary valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22408025
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0006344	small second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0008824	absent interventricular septum membranous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010017	visceral vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010018	pulmonary vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372253
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389319
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17468400
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372253
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010405	ostium secundum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389319
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17303760
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010457	pulmonary artery stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010595	abnormal aortic valve cusp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20150618	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010617	thick mitral valve cusps		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0010997	decreased aorta wall thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16242143
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372253
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12372254
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12454287
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15389319
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17468400
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17468400
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15107403
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:15680351
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0014731	disorganized myocardial fiber myofibrils		IAGP		N	RGD:5509061	20250904	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20201015	MGI			PMID:12372253
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0031584	thick semilunar valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:23288164
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:15297376
1553745	Hey2	hairy/enhancer-of-split related with YRPW motif 2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:23288164
1553746	Tssk5	testis-specific serine kinase 5	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1553751	Itpkc	inositol 1,4,5-trisphosphate 3-kinase C	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517551
1553751	Itpkc	inositol 1,4,5-trisphosphate 3-kinase C	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517551
1553751	Itpkc	inositol 1,4,5-trisphosphate 3-kinase C	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517551
1553751	Itpkc	inositol 1,4,5-trisphosphate 3-kinase C	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517551
1553751	Itpkc	inositol 1,4,5-trisphosphate 3-kinase C	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14517551
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049111
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000551	absent forelimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101846
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000557	absent hindlimb		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20251218	MGI			PMID:23806618
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832120
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000678	abnormal parathyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20150305	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20230727	MGI			PMID:24368733
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000836	abnormal substantia nigra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21832120
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20230727	MGI			PMID:24368733
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751172
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000865	absent cerebellum vermis		IAGP		N	RGD:5509061	20230727	MGI			PMID:24368733
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000867	abnormal cerebellum anterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751172
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000867	abnormal cerebellum anterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751172
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751172
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101845
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101845
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101845
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101845
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101845
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20843859
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003152	abnormal pillar cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574514
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574514
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12574514
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003395	abnormal subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003494	parathyroid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049111
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003631	nervous system phenotype		IAGP		N	RGD:5509061	20230727	MGI			PMID:24368733
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003854	abnormal forelimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101846
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003856	abnormal hindlimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101846
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003856	abnormal hindlimb stylopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101846
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003872	absent heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003873	pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003873	pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003877	abnormal serotonergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003931	absent molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004044	aortic dissection		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004160	retroesophageal right subclavian artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:15996652
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004161	cervical aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004161	cervical aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004312	absent pillar cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004318	absent incus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20231130	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004575	small limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101846
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20170921	MGI			PMID:15996652
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004861	abnormal Raphe nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049111
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0005029	abnormal amnion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049111
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364285
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11101846
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818193
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006331	abnormal patterning of the organ of Corti		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006346	small pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19855134
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:16308330
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009038	decreased inferior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10751172
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009038	decreased inferior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009039	absent inferior colliculus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480159
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009039	absent inferior colliculus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009048	enlarged tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18480159
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009844	abnormal neural crest cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009845	abnormal neural crest cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009893	cleft primary palate		IAGP		N	RGD:5509061	20150827	MGI			PMID:25381013
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010241	abnormal aortic arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12223416
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010527	bicuspid pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18832392
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10601039
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049111
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17557302
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23453598
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720879
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011262	abnormal pharyngeal arch mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011354	absent renal glomerulus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049111
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16049111
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462741
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19968985
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:12223416
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:15996652
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18818193
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0012179	abnormal splanchnic mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0012278	abnormal cardiogenic mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17507393
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10421635
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0012730	abnormal internal carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14975726
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0012752	abnormal cardiac neural crest cell migration		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0013268	second pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0013269	third pharyngeal arch hypoplasia		IAGP		N	RGD:5509061	20150924	MGI			PMID:20035084
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20150305	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0014044	absent cardiac outflow tract		IAGP		N	RGD:5509061	20160304	MGI			PMID:16720880
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0014281	hindlimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:16049111
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0021211	unilateral cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:25381013
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:25381013
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0030334	absent sixth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0030336	third pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0030337	enlarged third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0030340	absent fourth pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1553752	Fgf8	fibroblast growth factor 8	gene	MP:0030341	fourth pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1553755	Plcz1	phospholipase C, zeta 1	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20180125	MGI			PMID:28694258
1553755	Plcz1	phospholipase C, zeta 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1553755	Plcz1	phospholipase C, zeta 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20180125	MGI			PMID:28694258
1553755	Plcz1	phospholipase C, zeta 1	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1553755	Plcz1	phospholipase C, zeta 1	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20181227	MGI			
1553755	Plcz1	phospholipase C, zeta 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1553755	Plcz1	phospholipase C, zeta 1	gene	MP:0031013	abnormal egg activation		IAGP		N	RGD:5509061	20200130	MGI			PMID:28694258
1553755	Plcz1	phospholipase C, zeta 1	gene	MP:0031014	polyspermy		IAGP		N	RGD:5509061	20200130	MGI			PMID:28694258
1553757	Prkd2	protein kinase D2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:27670070
1553757	Prkd2	protein kinase D2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210826	MGI			
1553757	Prkd2	protein kinase D2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20200310	MGI			
1553757	Prkd2	protein kinase D2	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20819079
1553757	Prkd2	protein kinase D2	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20200310	MGI			
1553757	Prkd2	protein kinase D2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1553757	Prkd2	protein kinase D2	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20819079
1553757	Prkd2	protein kinase D2	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:27670070
1553757	Prkd2	protein kinase D2	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20819079
1553757	Prkd2	protein kinase D2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20200310	MGI			PMID:20819079
1553757	Prkd2	protein kinase D2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20819079
1553757	Prkd2	protein kinase D2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20819079
1553757	Prkd2	protein kinase D2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200310	MGI			
1553757	Prkd2	protein kinase D2	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20230601	MGI			
1553757	Prkd2	protein kinase D2	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20200310	MGI			
1553757	Prkd2	protein kinase D2	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20200310	MGI			PMID:27670070
1553758	Paqr9	progestin and adipoQ receptor family member IX	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20201015	MGI			PMID:30061575
1553763	Rxfp3	relaxin family peptide receptor 3	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1553763	Rxfp3	relaxin family peptide receptor 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1553763	Rxfp3	relaxin family peptide receptor 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20200310	MGI			PMID:25257104
1553763	Rxfp3	relaxin family peptide receptor 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25257104
1553763	Rxfp3	relaxin family peptide receptor 3	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
1553763	Rxfp3	relaxin family peptide receptor 3	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20230601	MGI			
1553769	Gda	guanine deaminase	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1553769	Gda	guanine deaminase	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20200402	MGI			
1553769	Gda	guanine deaminase	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1553769	Gda	guanine deaminase	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1553769	Gda	guanine deaminase	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1553769	Gda	guanine deaminase	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1553769	Gda	guanine deaminase	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20200402	MGI			
1553769	Gda	guanine deaminase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1553769	Gda	guanine deaminase	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20200402	MGI			
1553769	Gda	guanine deaminase	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
1553769	Gda	guanine deaminase	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1553769	Gda	guanine deaminase	gene	MP:0013764	decreased T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1553769	Gda	guanine deaminase	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20201231	MGI			
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0014467	increased sperm mitochondrial size		IAGP		N	RGD:5509061	20240613	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0030591	absent sperm fibrous sheath		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0031352	absent sperm axonemal central pair		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553771	Lrrc46	leucine rich repeat containing 46	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20221110	MGI			PMID:35955660
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0001202	skin photosensitivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:12509261
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0001203	increased sensitivity to skin irradiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12509261
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12509261
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20210520	MGI			
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210826	MGI			
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12509261
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22174697
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25762674
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:25762674
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0004501	increased incidence of tumors by UV-induction		IAGP		N	RGD:5509061	20200310	MGI			PMID:12509261
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210826	MGI			
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20200310	MGI			PMID:25762674
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:12509261
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:12509261
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:22174697
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200310	MGI			PMID:25762674
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0013787	photophobia		IAGP		N	RGD:5509061	20200310	MGI			PMID:12509261
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20240405	MGI			PMID:25762674
1553774	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:12509261
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20200310	MGI			PMID:20038601
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:23123064
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23123064
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0003957	abnormal nitric oxide homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20038601
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20038601
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:23123064
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23123064
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0008654	increased interleukin-1 alpha secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20038601
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20038601
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:20038601
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23123064
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23123064
1553776	Cd300lf	CD300 molecule like family member F	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:23123064
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000049	abnormal middle ear morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000081	premature cranial suture closure		IAGP		N	RGD:5509061	20200310	MGI			PMID:16502419
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15485632
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000623	decreased salivation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857655
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210520	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001306	small lens		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20231207	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001346	abnormal lacrimal gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15485632
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210826	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15485632
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15485632
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10661402
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:17622570
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10661402
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10454544
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:10454544
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20231207	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15485632
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857655
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:10454544
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857655
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0008879	submandibular gland inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0008880	lacrimal gland inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:15485632
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210826	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20231207	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21857655
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0010537	tumor regression		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0010835	increased CD4-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0010838	increased CD8-positive, alpha-beta memory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:10537105
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:21145943
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:9372963
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20200310	MGI			PMID:22522171
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0013367	parotid gland inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20932862
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20240405	MGI			PMID:34434211
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0020220	decreased tear production		IAGP		N	RGD:5509061	20200310	MGI			PMID:15485632
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1553777	Id3	inhibitor of DNA binding 3	gene	MP:0030410	middle ear effusion		IAGP		N	RGD:5509061	20211021	MGI			PMID:34434211
1553781	Paf1	Paf1, RNA polymerase II complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553781	Paf1	Paf1, RNA polymerase II complex component	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1553782	Ndufa10	NADH:ubiquinone oxidoreductase subunit A10	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200514	MGI			
1553782	Ndufa10	NADH:ubiquinone oxidoreductase subunit A10	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20201231	MGI			
1553782	Ndufa10	NADH:ubiquinone oxidoreductase subunit A10	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20200514	MGI			
1553782	Ndufa10	NADH:ubiquinone oxidoreductase subunit A10	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1553782	Ndufa10	NADH:ubiquinone oxidoreductase subunit A10	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1553782	Ndufa10	NADH:ubiquinone oxidoreductase subunit A10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553784	Adpgk	ADP-dependent glucokinase	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20200402	MGI			
1553784	Adpgk	ADP-dependent glucokinase	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200310	MGI			
1553784	Adpgk	ADP-dependent glucokinase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200310	MGI			
1553784	Adpgk	ADP-dependent glucokinase	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1553784	Adpgk	ADP-dependent glucokinase	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210520	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0005238	increased brain size		IEA		N	RGD:5509061	20210520	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17652091
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1553787	Gnptg	N-acetylglucosamine-1-phosphotransferase, gamma subunit	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20221103	MGI			
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210520	MGI			
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221103	MGI			
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15377789
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0003954	abnormal Reichert's membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15377789
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15377789
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15377789
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180830	MGI			PMID:29208648
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16467571
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20221103	MGI			
1553789	Plod3	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	gene	MP:0014239	abnormal intracellular organelle morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:15377789
1553792	Pxylp1	2-phosphoxylose phosphatase 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1553792	Pxylp1	2-phosphoxylose phosphatase 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20160804	MGI			
1553792	Pxylp1	2-phosphoxylose phosphatase 1	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1553792	Pxylp1	2-phosphoxylose phosphatase 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1553792	Pxylp1	2-phosphoxylose phosphatase 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1553792	Pxylp1	2-phosphoxylose phosphatase 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1553792	Pxylp1	2-phosphoxylose phosphatase 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20160804	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20220811	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20161201	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160804	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220519	MGI			
1553793	Dhx40	DEAH-box helicase 40	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553794	Tnfsf12	tumor necrosis factor (ligand) superfamily, member 12	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325585
1553797	Kif11	kinesin family member 11	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474226
1553797	Kif11	kinesin family member 11	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474226
1553797	Kif11	kinesin family member 11	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17449012
1553797	Kif11	kinesin family member 11	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474226
1553797	Kif11	kinesin family member 11	gene	MP:0006204	embryonic lethality before implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18474226
1553797	Kif11	kinesin family member 11	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17449012
1553797	Kif11	kinesin family member 11	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17449012
1553797	Kif11	kinesin family member 11	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17449012
1553797	Kif11	kinesin family member 11	gene	MP:0012111	failure of morula compaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17449012
1553804	Pfn2	profilin 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497369
1553804	Pfn2	profilin 2	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497369
1553804	Pfn2	profilin 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497369
1553804	Pfn2	profilin 2	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17541406
1553804	Pfn2	profilin 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497369
1553804	Pfn2	profilin 2	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17541406
1553804	Pfn2	profilin 2	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17541406
1553804	Pfn2	profilin 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:17541406
1553804	Pfn2	profilin 2	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17541406
1553804	Pfn2	profilin 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17541406
1553804	Pfn2	profilin 2	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17541406
1553804	Pfn2	profilin 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17541406
1553807	1700088E04Rik	RIKEN cDNA 1700088E04 gene	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210128	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001377	abnormal mating frequency		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20210128	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0002759	abnormal caudal vertebrae morphology		IEA		N	RGD:5509061	20220811	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210128	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0004909	increased seminal vesicle weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0004930	small epididymis		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:16024815
1553808	Aff4	AF4/FMR2 family, member 4	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1553809	Plpp5	phospholipid phosphatase 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:30042348
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000085	large anterior fontanelle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000128	growth retardation of molars		IAGP		N	RGD:5509061	20180215	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17194222
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664686
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000155	asymmetric rib joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664686
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664686
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:25889639
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342483
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16154126
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342483
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:16154126
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664686
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784057
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001292	abnormal lens vesicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16154126
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8792608
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784057
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8792608
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664686
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16154126
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17194222
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17194222
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002244	abnormal turbinate morphology		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784057
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20160804	MGI			
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784057
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:25889639
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002933	joint inflammation		IAGP		N	RGD:5509061	20150716	MGI			PMID:25889639
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342483
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003078	aphakia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003154	abnormal soft palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003445	sirenomelia		IAGP		N	RGD:5509061	20150716	MGI			PMID:23028455
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20150716	MGI			PMID:25889639
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342483
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:16154126
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003756	abnormal hard palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11470817
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004456	small pterygoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004458	absent alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004459	small alisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004467	absent zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004468	small zygomatic bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004574	broad limb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:8792608
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004612	fusion of vertebral bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664686
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664686
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004679	xiphoid process foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004757	abnormal distal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004790	absent upper incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784057
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004899	absent temporal bone squamous part		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004913	absent mandibular angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004934	epididymis epithelium degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784057
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0004935	epididymis degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784057
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005176	eyelids fail to open		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17194222
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342483
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005548	retina pigment epithelium atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784057
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0009003	abnormal vibrissa number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0009052	anal stenosis		IAGP		N	RGD:5509061	20150716	MGI			PMID:23028455
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17194222
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0009252	absent urinary bladder		IAGP		N	RGD:5509061	20150716	MGI			PMID:23028455
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0009782	abnormal basicranium angle		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0009883	palatal shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0010688	hair follicle outer root sheath hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0010985	abnormal kidney mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342483
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590254
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342483
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17260385
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9013703
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011387	absent metanephric mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:7590255
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0011846	decreased kidney collecting duct number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15342483
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19247966
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:10631182
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030026	small Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030121	small temporal bone squamous part		IAGP		N	RGD:5509061	20171005	MGI			PMID:22219353
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030199	deviated nasal septum		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030200	abnormal nasal septum cartilage morphology		IAGP		N	RGD:5509061	20171012	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030262	frontal bossing		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030313	abnormal face development		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030319	abnormal temporal bone petrous part morphology		IAGP		N	RGD:5509061	20171109	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030420	short basicranium		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030681	increased circulating hydroxyproline level		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030868	absent thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0030873	absent cricoid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:19127565
1553810	Bmp7	bone morphogenetic protein 7	gene	MP:0031101	nasal obstruction		IAGP		N	RGD:5509061	20210325	MGI			PMID:33431521
1553811	Ibtk	inhibitor of Bruton agammaglobulinemia tyrosine kinase	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21482705
1553812	Derl1	Der1-like domain family, member 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:22479592
1553812	Derl1	Der1-like domain family, member 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:22479592
1553817	Igsf5	immunoglobulin superfamily, member 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982697
1553818	Gemin2	gem nuclear organelle associated protein 2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091709
1553818	Gemin2	gem nuclear organelle associated protein 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12091709
1553819	Parp6	poly (ADP-ribose) polymerase family, member 6	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20220224	MGI			PMID:34067418
1553819	Parp6	poly (ADP-ribose) polymerase family, member 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20220224	MGI			PMID:34067418
1553819	Parp6	poly (ADP-ribose) polymerase family, member 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20220224	MGI			PMID:34067418
1553819	Parp6	poly (ADP-ribose) polymerase family, member 6	gene	MP:0001401	jumpy		IAGP		N	RGD:5509061	20220224	MGI			PMID:34067418
1553819	Parp6	poly (ADP-ribose) polymerase family, member 6	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20220224	MGI			PMID:34067418
1553819	Parp6	poly (ADP-ribose) polymerase family, member 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220224	MGI			PMID:34067418
1553819	Parp6	poly (ADP-ribose) polymerase family, member 6	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220224	MGI			PMID:34067418
1553822	Slc67a1	solute carrier family 67 member 1	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20240627	MGI			PMID:38626531
1553822	Slc67a1	solute carrier family 67 member 1	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:38626531
1553822	Slc67a1	solute carrier family 67 member 1	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20240627	MGI			PMID:38626531
1553824	Taar6	trace amine-associated receptor 6	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1553824	Taar6	trace amine-associated receptor 6	gene	MP:0005573	increased pulmonary respiratory rate		IEA		N	RGD:5509061	20201022	MGI			
1553824	Taar6	trace amine-associated receptor 6	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1553824	Taar6	trace amine-associated receptor 6	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1553824	Taar6	trace amine-associated receptor 6	gene	MP:0012125	decreased bronchoconstrictive response		IEA		N	RGD:5509061	20201022	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191205	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20241024	MGI			PMID:32376682
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191205	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0008993	abnormal portal triad morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191205	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191205	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20181227	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220519	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0013405	increased circulating lactate level		IAGP		N	RGD:5509061	20190509	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241128	MGI			
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:21274865
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0014967	increased liver enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0020836	increased circulating citrulline level		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0030650	increased circulating ornithine level		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0030662	decreased circulating arginine level		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0030970	ketosis		IAGP		N	RGD:5509061	20200213	MGI			PMID:28424480
1553825	Bcs1l	BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21274865
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:23593136
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20200310	MGI			PMID:23593136
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0003088	abnormal prepulse inhibition		IAGP		N	RGD:5509061	20200310	MGI			PMID:23593136
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0003822	decreased left ventricle systolic pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:23593136
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20200310	MGI			PMID:23593136
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0010695	abnormal blood pressure regulation		IAGP		N	RGD:5509061	20200310	MGI			PMID:20538684
1553828	Pdlim5	PDZ and LIM domain 5	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:20538684
1553829	Itga2	integrin alpha 2	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:12107118
1553829	Itga2	integrin alpha 2	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160421	MGI			
1553829	Itga2	integrin alpha 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788609
1553829	Itga2	integrin alpha 2	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788609
1553829	Itga2	integrin alpha 2	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618804
1553829	Itga2	integrin alpha 2	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359821
1553829	Itga2	integrin alpha 2	gene	MP:0008935	decreased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359821
1553829	Itga2	integrin alpha 2	gene	MP:0009548	abnormal platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788609
1553829	Itga2	integrin alpha 2	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788609
1553829	Itga2	integrin alpha 2	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359821
1553829	Itga2	integrin alpha 2	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:12107118
1553829	Itga2	integrin alpha 2	gene	MP:0014697	abnormal fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:16636073
1553829	Itga2	integrin alpha 2	gene	MP:0030578	decreased keratinocyte adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:16636073
1553831	Usp6nl	USP6 N-terminal like	gene	MP:0011709	increased fibroblast cell migration		IAGP		N	RGD:5509061	20200310	MGI			PMID:24239119
1553831	Usp6nl	USP6 N-terminal like	gene	MP:0020417	increased fibroblast chemotaxis		IAGP		N	RGD:5509061	20200310	MGI			PMID:24239119
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662942
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662942
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662942
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662942
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662942
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662942
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662942
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17662942
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:17662942
1553838	Mterf3	mitochondrial transcription termination factor 3	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:17662942
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0005094	abnormal T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0010134	decreased DN3 thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0012765	decreased alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:25201955
1553840	Noc2l	NOC2 like nucleolar associated transcriptional repressor	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:25201955
1553846	Mrps15	mitochondrial ribosomal protein S15	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1553846	Mrps15	mitochondrial ribosomal protein S15	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20260402	MGI			
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20250508	MGI			
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0013242	abnormal amino acid metabolism		IAGP		N	RGD:5509061	20160714	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0014998	abnormal glucose metabolism		IAGP		N	RGD:5509061	20260611	MGI			PMID:23716663
1553847	Letm1	leucine zipper-EF-hand containing transmembrane protein 1	gene	MP:0015000	decreased glucose oxidation		IAGP		N	RGD:5509061	20260611	MGI			PMID:23716663
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19447093
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:24725409
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:24725409
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:24725409
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20160324	MGI			PMID:24725409
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174357
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19447093
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174357
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001408	stereotypic behavior		IEA		N	RGD:5509061	20170105	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20111116	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20170105	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20170105	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20170105	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19447093
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19447093
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20141003	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20150108	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004399	abnormal cochlear outer hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20332152
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004431	abnormal hair cell mechanoelectric transduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19447093
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19447093
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849963
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20332152
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004577	abnormal cochlear hair cell inter-stereocilial links morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18339676
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0004578	abnormal cochlear hair bundle tip links morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19447093
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20201022	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174357
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19447093
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20150108	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17174357
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0008141	decreased small intestinal microvillus size		IAGP		N	RGD:5509061	20160324	MGI			PMID:24725409
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20141003	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20141003	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20141003	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20150108	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0011939	increased food intake		IEA		N	RGD:5509061	20211021	MGI			
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14519688
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19447093
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22381527
1553848	Ush1c	USH1 protein network component harmonin	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20211154
1553849	Ube2d3	ubiquitin-conjugating enzyme E2D 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1553849	Ube2d3	ubiquitin-conjugating enzyme E2D 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1553849	Ube2d3	ubiquitin-conjugating enzyme E2D 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20160421	MGI			
1553849	Ube2d3	ubiquitin-conjugating enzyme E2D 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1553849	Ube2d3	ubiquitin-conjugating enzyme E2D 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1553849	Ube2d3	ubiquitin-conjugating enzyme E2D 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1553854	Prickle3	prickle planar cell polarity protein 3	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32516135
1553854	Prickle3	prickle planar cell polarity protein 3	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32516135
1553854	Prickle3	prickle planar cell polarity protein 3	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32516135
1553854	Prickle3	prickle planar cell polarity protein 3	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32516135
1553854	Prickle3	prickle planar cell polarity protein 3	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20210415	MGI			PMID:32516135
1553854	Prickle3	prickle planar cell polarity protein 3	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32516135
1553854	Prickle3	prickle planar cell polarity protein 3	gene	MP:0020339	abnormal retina ganglion cell dendrite morphology		IAGP		N	RGD:5509061	20210415	MGI			PMID:32516135
1553854	Prickle3	prickle planar cell polarity protein 3	gene	MP:0031141	increased retina vascular tortuosity		IAGP		N	RGD:5509061	20210415	MGI			PMID:32516135
1553856	Klhl22	kelch-like 22	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20210826	MGI			
1553856	Klhl22	kelch-like 22	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1553856	Klhl22	kelch-like 22	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20211104	MGI			PMID:33109719
1553856	Klhl22	kelch-like 22	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1553856	Klhl22	kelch-like 22	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20211104	MGI			PMID:33109719
1553856	Klhl22	kelch-like 22	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20211104	MGI			PMID:33109719
1553856	Klhl22	kelch-like 22	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20211104	MGI			PMID:33109719
1553856	Klhl22	kelch-like 22	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20211104	MGI			PMID:33109719
1553857	Nipsnap3b	nipsnap homolog 3B	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1553857	Nipsnap3b	nipsnap homolog 3B	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1553857	Nipsnap3b	nipsnap homolog 3B	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20240523	MGI			
1553862	Paqr6	progestin and adipoQ receptor family member VI	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1553862	Paqr6	progestin and adipoQ receptor family member VI	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1553869	Tspan14	tetraspanin 14	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1553869	Tspan14	tetraspanin 14	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1553872	Chrdl1	chordin-like 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1553872	Chrdl1	chordin-like 1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20190718	MGI			PMID:30344043
1553872	Chrdl1	chordin-like 1	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20190718	MGI			PMID:30344043
1553872	Chrdl1	chordin-like 1	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:30344043
1553872	Chrdl1	chordin-like 1	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1553872	Chrdl1	chordin-like 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1553873	Lyzl4	lysozyme-like 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:27357688
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20240523	MGI			
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20240523	MGI			
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553878	Marchf2	membrane associated ring-CH-type finger 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210121	MGI			PMID:32935379
1553879	Orc4	origin recognition complex, subunit 4	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34977916
1553879	Orc4	origin recognition complex, subunit 4	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:34977916
1553879	Orc4	origin recognition complex, subunit 4	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:34977916
1553879	Orc4	origin recognition complex, subunit 4	gene	MP:0012736	abnormal polar body morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:34977916
1553882	Oas1h	2'-5' oligoadenylate synthetase 1H	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240613	MGI			PMID:38786026
1553883	Bmf	BCL2 modifying factor	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0001144	vagina atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0003537	hydrometrocolpos		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20161013	MGI			PMID:27044867
1553883	Bmf	BCL2 modifying factor	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0006414	decreased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18299399
1553883	Bmf	BCL2 modifying factor	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553883	Bmf	BCL2 modifying factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19841067
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26245904
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:26245904
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:26245904
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:26245904
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20200310	MGI			PMID:26245904
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20220811	MGI			
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1553884	Neil2	nei like 2 (E. coli)	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20200310	MGI			PMID:26245904
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23709686
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23709686
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23709686
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23709686
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008615	decreased circulating interleukin-17 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23709686
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008680	abnormal interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23709686
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23709686
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23602766
1553885	Clec4d	C-type lectin domain family 4, member d	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23709686
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553887	Serpina12	serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22837305
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20230601	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20230601	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230119	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230601	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20230119	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20241121	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20230119	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0009906	increased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:10932185
1553888	Ryk	receptor-like tyrosine kinase	gene	MP:0030315	small neurocranium		IAGP		N	RGD:5509061	20171109	MGI			PMID:10932185
15554233	Gm26330	predicted gene, 26330	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15554233	Gm26330	predicted gene, 26330	gene	MP:0011941	increased fluid intake		IAGP		N	RGD:5509061	20231109	MGI			PMID:37329887
15557747	Snord50b	small nucleolar RNA, C/D box 50B	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557747	Snord50b	small nucleolar RNA, C/D box 50B	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557747	Snord50b	small nucleolar RNA, C/D box 50B	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557747	Snord50b	small nucleolar RNA, C/D box 50B	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557747	Snord50b	small nucleolar RNA, C/D box 50B	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557747	Snord50b	small nucleolar RNA, C/D box 50B	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557755	Snord50a	small nucleolar RNA, C/D box 50A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557755	Snord50a	small nucleolar RNA, C/D box 50A	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557755	Snord50a	small nucleolar RNA, C/D box 50A	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557755	Snord50a	small nucleolar RNA, C/D box 50A	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557755	Snord50a	small nucleolar RNA, C/D box 50A	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
15557755	Snord50a	small nucleolar RNA, C/D box 50A	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20201029	MGI			PMID:23991050
1556860	Itm2a	integral membrane protein 2A	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650549
1556860	Itm2a	integral membrane protein 2A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23650549
1556861	Glb1l3	galactosidase, beta 1 like 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20221215	MGI			
1556861	Glb1l3	galactosidase, beta 1 like 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20231207	MGI			
1556862	Tsnaxip1	translin-associated factor X (Tsnax) interacting protein 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20231012	MGI			PMID:36598146
1556862	Tsnaxip1	translin-associated factor X (Tsnax) interacting protein 1	gene	MP:0009282	decreased hyperactivated sperm motility		IAGP		N	RGD:5509061	20231012	MGI			PMID:36598146
1556862	Tsnaxip1	translin-associated factor X (Tsnax) interacting protein 1	gene	MP:0014803	abnormal flagellar waveform		IAGP		N	RGD:5509061	20251120	MGI			PMID:36598146
1556862	Tsnaxip1	translin-associated factor X (Tsnax) interacting protein 1	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20231012	MGI			PMID:36598146
1556865	Il22	interleukin 22	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1556865	Il22	interleukin 22	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264109
1556865	Il22	interleukin 22	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:24211183
1556865	Il22	interleukin 22	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:17187052
1556865	Il22	interleukin 22	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17187052
1556865	Il22	interleukin 22	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264109
1556865	Il22	interleukin 22	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1556865	Il22	interleukin 22	gene	MP:0001655	multifocal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264109
1556865	Il22	interleukin 22	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17187052
1556865	Il22	interleukin 22	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919941
1556865	Il22	interleukin 22	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1556865	Il22	interleukin 22	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17187052
1556865	Il22	interleukin 22	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23223145
1556865	Il22	interleukin 22	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20150514	MGI			PMID:25261485
1556865	Il22	interleukin 22	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264109
1556865	Il22	interleukin 22	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23223145
1556865	Il22	interleukin 22	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919941
1556865	Il22	interleukin 22	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17187052
1556865	Il22	interleukin 22	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1556865	Il22	interleukin 22	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1556865	Il22	interleukin 22	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23075849
1556865	Il22	interleukin 22	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264109
1556865	Il22	interleukin 22	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24211183
1556865	Il22	interleukin 22	gene	MP:0005023	abnormal wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23223145
1556865	Il22	interleukin 22	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919941
1556865	Il22	interleukin 22	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1556865	Il22	interleukin 22	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23075849
1556865	Il22	interleukin 22	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1556865	Il22	interleukin 22	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1556865	Il22	interleukin 22	gene	MP:0008618	decreased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1556865	Il22	interleukin 22	gene	MP:0008639	decreased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1556865	Il22	interleukin 22	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1556865	Il22	interleukin 22	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1556865	Il22	interleukin 22	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919941
1556865	Il22	interleukin 22	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17919941
1556865	Il22	interleukin 22	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23064362
1556865	Il22	interleukin 22	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1556865	Il22	interleukin 22	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18264109
1556865	Il22	interleukin 22	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20150514	MGI			PMID:25261485
1556865	Il22	interleukin 22	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1556865	Il22	interleukin 22	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24211183
1556865	Il22	interleukin 22	gene	MP:0012424	decreased alimentary system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23075849
1556865	Il22	interleukin 22	gene	MP:0020186	abnormal susceptibility to bacterial infection		IAGP		N	RGD:5509061	20150514	MGI			PMID:25261485
1556866	Phlpp2	PH domain and leucine rich repeat protein phosphatase 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1556866	Phlpp2	PH domain and leucine rich repeat protein phosphatase 2	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20160929	MGI			PMID:26187040
1556866	Phlpp2	PH domain and leucine rich repeat protein phosphatase 2	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20160929	MGI			PMID:26187040
1556867	Anks1b	ankyrin repeat and sterile alpha motif domain containing 1B	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20170817	MGI			PMID:28115237
1556867	Anks1b	ankyrin repeat and sterile alpha motif domain containing 1B	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20160707	MGI			PMID:26085624
1556867	Anks1b	ankyrin repeat and sterile alpha motif domain containing 1B	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20160707	MGI			PMID:26085624
1556867	Anks1b	ankyrin repeat and sterile alpha motif domain containing 1B	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20170817	MGI			PMID:28115237
1556867	Anks1b	ankyrin repeat and sterile alpha motif domain containing 1B	gene	MP:0009746	enhanced behavioral response to xenobiotic		IAGP		N	RGD:5509061	20170817	MGI			PMID:28115237
1556867	Anks1b	ankyrin repeat and sterile alpha motif domain containing 1B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170817	MGI			PMID:28115237
1556867	Anks1b	ankyrin repeat and sterile alpha motif domain containing 1B	gene	MP:0011274	short excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20160707	MGI			PMID:26085624
1556867	Anks1b	ankyrin repeat and sterile alpha motif domain containing 1B	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:28115237
1556868	Or55b4	olfactory receptor family 55 subfamily B member 4	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20240314	MGI			PMID:28990936
1556870	Cep72	centrosomal protein 72	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556870	Cep72	centrosomal protein 72	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20221229	MGI			PMID:36277211
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0008910	thin long bone epiphysis		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556873	Csgalnact2	chondroitin sulfate N-acetylgalactosaminyltransferase 2	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20180308	MGI			PMID:29287114
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0000445	short snout		IEA		N	RGD:5509061	20141003	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0000644	dextrocardia		IEA		N	RGD:5509061	20111116	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0000694	spleen hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906869
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0001947	abnormal mucociliary clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19675306
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0001950	abnormal respiratory sounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498047
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19675306
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191205	MGI			PMID:26501274
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20141003	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0003178	left pulmonary isomerism		IEA		N	RGD:5509061	20141003	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906869
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0010463	aorta stenosis		IEA		N	RGD:5509061	20141003	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0011249	abdominal situs inversus		IEA		N	RGD:5509061	20141003	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0011250	abdominal situs ambiguus		IEA		N	RGD:5509061	20111116	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0011251	bronchial situs inversus		IEA		N	RGD:5509061	20111116	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0011649	immotile respiratory cilia		IEA		N	RGD:5509061	20141003	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20141003	MGI			
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19906869
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0013206	abnormal motile cilium morphology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0013209	abnormal motile cilium physiology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24306492
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0030118	rhinosinusitis		IAGP		N	RGD:5509061	20210211	MGI			PMID:19675306
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0031088	coughing		IAGP		N	RGD:5509061	20210211	MGI			PMID:20498047
1556874	Dnai1	dynein axonemal intermediate chain 1	gene	MP:0031089	sneezing		IAGP		N	RGD:5509061	20210211	MGI			PMID:20498047
1556875	Plin4	perilipin 4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1556875	Plin4	perilipin 4	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20230601	MGI			
1556875	Plin4	perilipin 4	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230601	MGI			
1556875	Plin4	perilipin 4	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230601	MGI			
1556875	Plin4	perilipin 4	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230601	MGI			
1556875	Plin4	perilipin 4	gene	MP:0031417	decreased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23423172
1556876	Aig1	androgen-induced 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20210114	MGI			PMID:32152231
1556876	Aig1	androgen-induced 1	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20210114	MGI			PMID:32152231
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20170105	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000603	pale liver		IEA		N	RGD:5509061	20210520	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20170105	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160114	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074523
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20160811	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20463034
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074523
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0004111	abnormal coronary artery morphology		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20160114	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0004848	abnormal liver size		IEA		N	RGD:5509061	20160811	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20220519	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0005650	abnormal limb bud morphology		IEA		N	RGD:5509061	20160114	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074523
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074523
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074523
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0009131	decreased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074523
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20074523
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20170309	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0010473	descending aorta dilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0010476	coronary fistula		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0010479	brain aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16155214
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16459298
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20463034
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20160616	MGI			PMID:25760946
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160114	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20141003	MGI			
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17452975
1556878	Sufu	SUFU negative regulator of hedgehog signaling	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784869
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784869
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0001740	failure of adrenal epinephrine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784869
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20201231	MGI			
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784869
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784869
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20190502	MGI			
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784869
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0008247	abnormal mononuclear cell morphology		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784869
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11784869
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0012574	decreased noradrenaline level		IAGP		N	RGD:5509061	20180927	MGI			PMID:11784869
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556880	Ly6e	lymphocyte antigen 6 family member E	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200820	MGI			PMID:32704094
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0003393	decreased cardiac output		IEA		N	RGD:5509061	20240523	MGI			
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20250508	MGI			
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0003992	increased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16427009
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0011952	decreased cardiac stroke volume		IEA		N	RGD:5509061	20240523	MGI			
1556882	Mdc1	mediator of DNA damage checkpoint 1	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:16427009
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20160204	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0000126	brittle teeth		IAGP		N	RGD:5509061	20160204	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20211014	MGI			PMID:27283840
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20211014	MGI			PMID:27283840
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0001868	ovary inflammation		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0001927	abnormal estrous cycle		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20160204	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20211014	MGI			PMID:27283840
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20201022	MGI			
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0003507	abnormal ovary physiology		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20170921	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20211014	MGI			PMID:27283840
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0008837	increased transforming growth factor beta level		IAGP		N	RGD:5509061	20211014	MGI			PMID:27283840
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0009010	abnormal diestrus		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0009018	short estrus		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0009020	prolonged metestrus		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0011124	increased primary ovarian follicle number		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0011951	increased cardiac stroke volume		IEA		N	RGD:5509061	20200402	MGI			
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0014431	increased chemokine level		IAGP		N	RGD:5509061	20260219	MGI			PMID:27283840
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0020011	increased bone mineral density of femur		IAGP		N	RGD:5509061	20220922	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0021106	abnormal secondary ovarian follicle morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0030080	small lower incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0030081	small upper incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0030089	short lower incisors		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0030090	short upper incisors		IAGP		N	RGD:5509061	20220616	MGI			PMID:34333627
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0030458	abnormal tooth wear		IAGP		N	RGD:5509061	20180125	MGI			PMID:24686385
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0031215	abnormal response to myocardial ischemic injury		IAGP		N	RGD:5509061	20211014	MGI			PMID:27283840
1556883	Grem2	gremlin 2, DAN family BMP antagonist	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:27283840
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0003305	proctitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18318596
1556884	Il10rb	interleukin 10 receptor, beta	gene	MP:0011224	abnormal lymph node medullary cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9463407
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0000032	cochlear degeneration		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200402	MGI			
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20170105	MGI			
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20250626	MGI			PMID:37943620
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004465	degeneration of organ of Corti supporting cells		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004737	absent distortion product otoacoustic emissions		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0004749	nonsyndromic hearing loss		IAGP		N	RGD:5509061	20250626	MGI			PMID:37943620
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20250626	MGI			PMID:37943620
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0011968	decreased threshold for auditory brainstem response		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0014406	increased or absent distortion product otoacoustic emission threshold		IAGP		N	RGD:5509061	20250626	MGI			PMID:37943620
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0020352	abnormal endoplasmic reticulum physiology		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556885	Tmtc4	transmembrane and tetratricopeptide repeat containing 4	gene	MP:0020354	increased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20190307	MGI			PMID:30188326
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001059	optic nerve atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001512	trunk curl		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002338	abnormal pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0003382	straub tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0004142	abnormal muscle tone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005356	positive geotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005507	tail dragging		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460290
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005604	hyperekplexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0005656	decreased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0006051	brainstem hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20170309	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0009947	abnormal olfactory bulb external plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0009964	abnormal cerebellum lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0009983	abnormal cerebellum fastigial nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0010047	axonal spheroids		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0010323	retropulsion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0010746	abnormal pre-Botzinger complex physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22653057
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19460290
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:18396137
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:23702311
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0014910	decreased hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:20534480
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0030655	increased circulating glycine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0030670	increased circulating phenylalanine level		IAGP		N	RGD:5509061	20180920	MGI			PMID:22535952
1556886	Ndufs4	NADH:ubiquinone oxidoreductase core subunit S4	gene	MP:0030745	increased circulating homocitrulline level		IAGP		N	RGD:5509061	20240912	MGI			PMID:22535952
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0002219	decreased lymph node number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902460
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20230119	MGI			
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902460
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12902460
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20150702	MGI			
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0008201	absent follicular dendritic cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10917533
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20240523	MGI			
1556887	Cxcl13	C-X-C motif chemokine ligand 13	gene	MP:0014472	impaired B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:17185562
1556889	Dock6	dedicator of cytokinesis 6	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1556889	Dock6	dedicator of cytokinesis 6	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1556889	Dock6	dedicator of cytokinesis 6	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1556889	Dock6	dedicator of cytokinesis 6	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1556890	Hoxc8	homeobox C8	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19621436
1556890	Hoxc8	homeobox C8	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510925
1556890	Hoxc8	homeobox C8	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0003807	camptodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19621436
1556890	Hoxc8	homeobox C8	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510925
1556890	Hoxc8	homeobox C8	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556890	Hoxc8	homeobox C8	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19621436
1556890	Hoxc8	homeobox C8	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1348969
1556890	Hoxc8	homeobox C8	gene	MP:0012284	increased sternebra number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1556891	Rusc1	RUN and SH3 domain containing 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20181227	MGI			
1556891	Rusc1	RUN and SH3 domain containing 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1556891	Rusc1	RUN and SH3 domain containing 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1556891	Rusc1	RUN and SH3 domain containing 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1556891	Rusc1	RUN and SH3 domain containing 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1556891	Rusc1	RUN and SH3 domain containing 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220519	MGI			
1556892	Rasgrp2	RAS, guanyl releasing protein 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20151217	MGI			PMID:17492052
1556892	Rasgrp2	RAS, guanyl releasing protein 2	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15334074
1556892	Rasgrp2	RAS, guanyl releasing protein 2	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:15334074
1556892	Rasgrp2	RAS, guanyl releasing protein 2	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20151217	MGI			PMID:17492052
1556892	Rasgrp2	RAS, guanyl releasing protein 2	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15334074
1556892	Rasgrp2	RAS, guanyl releasing protein 2	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20151217	MGI			PMID:17492052
1556892	Rasgrp2	RAS, guanyl releasing protein 2	gene	MP:0009676	abnormal hemostasis		IAGP		N	RGD:5509061	20191212	MGI			PMID:25705885
1556892	Rasgrp2	RAS, guanyl releasing protein 2	gene	MP:0011898	abnormal platelet cell number		IAGP		N	RGD:5509061	20191212	MGI			PMID:25705885
1556894	Cd33	CD33 molecule	gene	MP:0001586	abnormal erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773563
1556894	Cd33	CD33 molecule	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773563
1556894	Cd33	CD33 molecule	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773563
1556894	Cd33	CD33 molecule	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20230119	MGI			
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0001713	decreased trophoblast giant cell number		IEA		N	RGD:5509061	20241010	MGI			
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0001727	abnormal embryo implantation		IEA		N	RGD:5509061	20241010	MGI			
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20230119	MGI			
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20150212	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20230119	MGI			
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0012505	increased neural tube apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:17374848
1556895	Rad54l2	RAD54 like 2 (S. cerevisiae)	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0009567	mitotic nondisjunction		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0010898	abnormal pulmonary alveolus epithelium morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0010900	abnormal pulmonary interalveolar septum morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20201210	MGI			PMID:32321712
1556899	Hnrnpa3	heterogeneous nuclear ribonucleoprotein A3	gene	MP:0015020	thin cerebral cortex layer		IAGP		N	RGD:5509061	20260716	MGI			PMID:32321712
1556900	Ankrd49	ankyrin repeat domain 49	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20250508	MGI			
1556900	Ankrd49	ankyrin repeat domain 49	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20250508	MGI			
1556900	Ankrd49	ankyrin repeat domain 49	gene	MP:0004085	abnormal heartbeat		IEA		N	RGD:5509061	20250508	MGI			
1556900	Ankrd49	ankyrin repeat domain 49	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1556901	Mrgprx1	MAS-related GPR, member X1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1556901	Mrgprx1	MAS-related GPR, member X1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20240530	MGI			PMID:33358893
1556901	Mrgprx1	MAS-related GPR, member X1	gene	MP:0010073	decreased pruritus		IAGP		N	RGD:5509061	20240530	MGI			PMID:33358893
1556902	Foxo4	forkhead box O4	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210520	MGI			
1556902	Foxo4	forkhead box O4	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20150618	MGI			PMID:25264246
1556902	Foxo4	forkhead box O4	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1556902	Foxo4	forkhead box O4	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0002047	increased hepatic hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20150618	MGI			PMID:25264246
1556902	Foxo4	forkhead box O4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14978268
1556902	Foxo4	forkhead box O4	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20150618	MGI			PMID:25264246
1556902	Foxo4	forkhead box O4	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20150618	MGI			PMID:25264246
1556902	Foxo4	forkhead box O4	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20150618	MGI			PMID:25264246
1556902	Foxo4	forkhead box O4	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20150618	MGI			PMID:25264246
1556902	Foxo4	forkhead box O4	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20150618	MGI			PMID:25264246
1556902	Foxo4	forkhead box O4	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20150618	MGI			PMID:25264246
1556902	Foxo4	forkhead box O4	gene	MP:0009442	increased ovarian teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0010306	increased hamartoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556902	Foxo4	forkhead box O4	gene	MP:0012437	increased Harderian gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254969
1556904	Tuba8	tubulin, alpha 8	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1556904	Tuba8	tubulin, alpha 8	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20241121	MGI			
1556904	Tuba8	tubulin, alpha 8	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1556904	Tuba8	tubulin, alpha 8	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20241121	MGI			
1556904	Tuba8	tubulin, alpha 8	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1556904	Tuba8	tubulin, alpha 8	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1556904	Tuba8	tubulin, alpha 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20171214	MGI			PMID:28388629
1556904	Tuba8	tubulin, alpha 8	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1556906	Tasl	TLR adaptor interacting with endolysosomal SLC15A4	gene	MP:0001819	abnormal immune cell physiology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39856038
1556906	Tasl	TLR adaptor interacting with endolysosomal SLC15A4	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20250605	MGI			PMID:39856038
1556906	Tasl	TLR adaptor interacting with endolysosomal SLC15A4	gene	MP:0014436	decreased interferon level		IAGP		N	RGD:5509061	20250605	MGI			PMID:39856038
1556907	Zfp28	zinc finger protein 28	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20240523	MGI			
1556907	Zfp28	zinc finger protein 28	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1556910	Slc5a8	solute carrier family 5 (iodide transporter), member 8	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18562324
1556910	Slc5a8	solute carrier family 5 (iodide transporter), member 8	gene	MP:0005310	abnormal salivary gland physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18562324
1556910	Slc5a8	solute carrier family 5 (iodide transporter), member 8	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18562324
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210826	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20201231	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20201022	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20200514	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20201022	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20210826	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230601	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20200514	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20201022	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20201022	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210128	MGI			
1556911	Gpr146	G protein-coupled receptor 146	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20201022	MGI			
1556912	Cdyl	chromodomain protein, Y chromosome-like	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20180329	MGI			PMID:28076783
1556912	Cdyl	chromodomain protein, Y chromosome-like	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20180329	MGI			PMID:28076783
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0000126	brittle teeth		IAGP		N	RGD:5509061	20171228	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0002649	abnormal enamel rod pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0004830	short incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728677
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0009790	decreased susceptibility to viral infection induced morbidity/mortality		IAGP		N	RGD:5509061	20260305	MGI			PMID:38030279
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0010096	abnormal incisor color		IAGP		N	RGD:5509061	20141003	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0014165	absent ciliary process		IAGP		N	RGD:5509061	20160414	MGI			PMID:15728677
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0014175	abnormal ciliary epithelium morphology		IAGP		N	RGD:5509061	20160505	MGI			PMID:15728677
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0030138	abnormal lower incisor color		IAGP		N	RGD:5509061	20171005	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0030450	abnormal enamel mineralization		IAGP		N	RGD:5509061	20171221	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0030458	abnormal tooth wear		IAGP		N	RGD:5509061	20171228	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0030459	abnormal tooth attrition		IAGP		N	RGD:5509061	20171228	MGI			PMID:18703497
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0030500	conical molar		IAGP		N	RGD:5509061	20180118	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0030522	abnormal stellate reticulum morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:21038445
1556913	Nectin1	nectin cell adhesion molecule 1	gene	MP:0030523	abnormal stratum intermedium morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:21038445
1556917	Atg9b	autophagy related 9B	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20181227	MGI			
1556917	Atg9b	autophagy related 9B	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20181227	MGI			
1556917	Atg9b	autophagy related 9B	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1556917	Atg9b	autophagy related 9B	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1556918	Plekha2	pleckstrin homology domain containing A2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21204784
1556918	Plekha2	pleckstrin homology domain containing A2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21204784
1556918	Plekha2	pleckstrin homology domain containing A2	gene	MP:0030018	increased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:21204784
1556918	Plekha2	pleckstrin homology domain containing A2	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:21204784
1556919	Atrnl1	attractin like 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1556919	Atrnl1	attractin like 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18064672
1556919	Atrnl1	attractin like 1	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18064672
1556919	Atrnl1	attractin like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20250116	MGI			PMID:39037895
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20260416	MGI			PMID:41507200
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20260416	MGI			PMID:41507200
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250116	MGI			PMID:39037895
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20260416	MGI			PMID:41507200
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20250116	MGI			PMID:39037895
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20260416	MGI			PMID:41507200
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20260416	MGI			PMID:41507200
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0003631	nervous system phenotype		IAGP		N	RGD:5509061	20250116	MGI			PMID:39037895
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20250116	MGI			PMID:39037895
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20250116	MGI			PMID:39037895
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20260416	MGI			PMID:41507200
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20250116	MGI			PMID:39037895
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0012203	abnormal neuronal stem cell morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:25070536
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20260416	MGI			PMID:41507200
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20260416	MGI			PMID:41507200
1556922	Pqbp1	polyglutamine binding protein 1	gene	MP:0020596	decreased cerebral cortex total cell area		IAGP		N	RGD:5509061	20260416	MGI			PMID:41507200
1556924	H2-Ob	histocompatibility 2, O region beta locus	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20180802	MGI			PMID:10684291
1556924	H2-Ob	histocompatibility 2, O region beta locus	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20180802	MGI			PMID:12538662
1556924	H2-Ob	histocompatibility 2, O region beta locus	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20180802	MGI			PMID:10684291
1556924	H2-Ob	histocompatibility 2, O region beta locus	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20180802	MGI			PMID:12538662
1556924	H2-Ob	histocompatibility 2, O region beta locus	gene	MP:0005043	defective assembly of class II molecules		IAGP		N	RGD:5509061	20180809	MGI			PMID:28813660
1556924	H2-Ob	histocompatibility 2, O region beta locus	gene	MP:0020935	decreased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18057254
1556924	H2-Ob	histocompatibility 2, O region beta locus	gene	MP:0020935	decreased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:28813660
1556928	Oas1b	2'-5' oligoadenylate synthetase 1B	gene	MP:0020943	increased susceptibility to Flaviviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16589143
1556928	Oas1b	2'-5' oligoadenylate synthetase 1B	gene	MP:0020944	decreased susceptibility to Flaviviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16589143
1556928	Oas1b	2'-5' oligoadenylate synthetase 1B	gene	MP:0020944	decreased susceptibility to Flaviviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17904183
1556928	Oas1b	2'-5' oligoadenylate synthetase 1B	gene	MP:0020944	decreased susceptibility to Flaviviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:8380081
1556931	Hoxb5	homeobox B5	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1556931	Hoxb5	homeobox B5	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1556931	Hoxb5	homeobox B5	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1556931	Hoxb5	homeobox B5	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1556931	Hoxb5	homeobox B5	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0004173	abnormal intervertebral disk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0004508	abnormal pectoral girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1556931	Hoxb5	homeobox B5	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1556931	Hoxb5	homeobox B5	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1556931	Hoxb5	homeobox B5	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556931	Hoxb5	homeobox B5	gene	MP:0012668	absent sternal manubrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20211021	MGI			PMID:29944857
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190711	MGI			PMID:29944857
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20190711	MGI			PMID:29944857
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20190711	MGI			PMID:29944857
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20211021	MGI			PMID:26493479
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20190711	MGI			PMID:29944857
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20211021	MGI			PMID:26493479
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20211021	MGI			PMID:26493479
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20211021	MGI			PMID:26493479
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0011995	decreased leukemia incidence		IAGP		N	RGD:5509061	20211021	MGI			PMID:26493479
1556934	Zdhhc9	zinc finger, DHHC domain containing 9	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20190711	MGI			PMID:29944857
1556936	Oscar	osteoclast associated receptor	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841309
1556936	Oscar	osteoclast associated receptor	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841309
1556936	Oscar	osteoclast associated receptor	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841309
1556936	Oscar	osteoclast associated receptor	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841309
1556936	Oscar	osteoclast associated receptor	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841309
1556936	Oscar	osteoclast associated receptor	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1556936	Oscar	osteoclast associated receptor	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841309
1556936	Oscar	osteoclast associated receptor	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21841309
1556937	Polr1e	polymerase (RNA) I polypeptide E	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1556937	Polr1e	polymerase (RNA) I polypeptide E	gene	MP:0003345	decreased rib number		IEA		N	RGD:5509061	20160804	MGI			
1556937	Polr1e	polymerase (RNA) I polypeptide E	gene	MP:0004647	decreased lumbar vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1556937	Polr1e	polymerase (RNA) I polypeptide E	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1556937	Polr1e	polymerase (RNA) I polypeptide E	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:10982834
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:11457897
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:18792399
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20180719	MGI			PMID:11457897
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0005672	increased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20180719	MGI			PMID:18792399
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20180719	MGI			PMID:11457897
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556938	Lilrb4a	leukocyte immunoglobulin-like receptor, subfamily B, member 4A	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20180719	MGI			PMID:17761953
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0000003	abnormal adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962829
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0000659	prostate gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19185849
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001168	abnormal prostate gland epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19185849
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:19185849
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962829
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141160
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962829
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19185849
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19046572
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962829
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141160
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962829
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0004893	decreased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962829
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0009734	abnormal prostate gland duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19185849
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:19497867
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0010130	decreased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0010134	decreased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22815285
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962829
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17043309
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141160
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962829
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16962829
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0011524	thick placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17141160
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20150611	MGI			PMID:21266327
1556939	Rictor	RPTOR independent companion of MTOR, complex 2	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:19497867
1556940	Ces5a	carboxylesterase 5A	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1556940	Ces5a	carboxylesterase 5A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1556940	Ces5a	carboxylesterase 5A	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210506	MGI			PMID:32814578
1556940	Ces5a	carboxylesterase 5A	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:32814578
1556940	Ces5a	carboxylesterase 5A	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:32814578
1556940	Ces5a	carboxylesterase 5A	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:32814578
1556940	Ces5a	carboxylesterase 5A	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1556940	Ces5a	carboxylesterase 5A	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1556940	Ces5a	carboxylesterase 5A	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1556940	Ces5a	carboxylesterase 5A	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1556940	Ces5a	carboxylesterase 5A	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210506	MGI			PMID:32814578
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0000122	premature tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371931
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20111116	MGI			
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371931
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371931
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0002082	postnatal lethality		IEA		N	RGD:5509061	20111116	MGI			
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371931
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:1385849
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8636651
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003670	dilated renal glomerular capsule		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872122
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:1385849
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371931
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0003985	renal fibrosis		IEA		N	RGD:5509061	20111116	MGI			
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1385849
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1385849
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1385849
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:3712587
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0006084	abnormal circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1385849
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:8636651
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0009051	dilated distal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210520	MGI			
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0010478	intracranial aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:1883968
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371931
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371931
1556941	Nphp3	nephronophthisis 3 (adolescent)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1556942	Rnft2	ring finger protein, transmembrane 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1556942	Rnft2	ring finger protein, transmembrane 2	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20241121	MGI			
1556942	Rnft2	ring finger protein, transmembrane 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20241121	MGI			
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0002685	abnormal spermatogonia proliferation		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0014617	decreased spermatogonia number		IAGP		N	RGD:5509061	20250220	MGI			PMID:34825148
1556943	Rpl39l	ribosomal protein L39-like	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20220210	MGI			PMID:34825148
1556946	Bdp1	B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20220519	MGI			
1556946	Bdp1	B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210826	MGI			
1556946	Bdp1	B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1556946	Bdp1	B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1556946	Bdp1	B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1556946	Bdp1	B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1556946	Bdp1	B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20241121	MGI			
1556946	Bdp1	B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1556948	Helt	helt bHLH transcription factor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968817
1556948	Helt	helt bHLH transcription factor	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968817
1556948	Helt	helt bHLH transcription factor	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968817
1556948	Helt	helt bHLH transcription factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968817
1556948	Helt	helt bHLH transcription factor	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968817
1556948	Helt	helt bHLH transcription factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968817
1556948	Helt	helt bHLH transcription factor	gene	MP:0003246	loss of GABAergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968817
1556948	Helt	helt bHLH transcription factor	gene	MP:0003246	loss of GABAergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17611227
1556948	Helt	helt bHLH transcription factor	gene	MP:0003247	abnormal glutaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17611227
1556948	Helt	helt bHLH transcription factor	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968817
1556948	Helt	helt bHLH transcription factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968817
1556952	Leo1	Leo1, Paf1/RNA polymerase II complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:30372477
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20190103	MGI			PMID:30372477
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20190103	MGI			PMID:30372477
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:35238077
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20221103	MGI			PMID:35238077
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20240523	MGI			
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20190103	MGI			PMID:30372477
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0001994	increased blinking frequency		IAGP		N	RGD:5509061	20221103	MGI			PMID:35238077
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:30372477
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0005252	abnormal Meibomian gland morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:35238077
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20221103	MGI			PMID:35238077
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0009535	abnormal skin sebaceous gland morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:30372477
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0012725	small sebaceous gland		IAGP		N	RGD:5509061	20190103	MGI			PMID:30372477
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0013376	abnormal sebocyte differentiation		IAGP		N	RGD:5509061	20190103	MGI			PMID:30372477
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0013391	abnormal Meibomian gland physiology		IAGP		N	RGD:5509061	20221103	MGI			PMID:35238077
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0014131	abnormal tear film morphology		IAGP		N	RGD:5509061	20221103	MGI			PMID:35238077
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0014132	abnormal tear film physiology		IAGP		N	RGD:5509061	20221103	MGI			PMID:35238077
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0020219	increased tear production		IAGP		N	RGD:5509061	20221103	MGI			PMID:35238077
1556953	Far2	fatty acyl CoA reductase 2	gene	MP:0030572	abnormal pilosebaceous unit morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:30372477
1556954	Lrrc2	leucine rich repeat containing 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220519	MGI			
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20170209	MGI			PMID:27502165
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:25729399
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:27502165
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20160804	MGI			
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20220901	MGI			PMID:32241915
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20220901	MGI			PMID:32241915
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27502165
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27502165
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20220901	MGI			PMID:32241915
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27502165
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27502165
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20170209	MGI			PMID:27502165
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0008191	abnormal follicular B cell physiology		IAGP		N	RGD:5509061	20170209	MGI			PMID:27502165
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20210429	MGI			PMID:25729399
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20220901	MGI			PMID:32241915
1556955	Dock10	dedicator of cytokinesis 10	gene	MP:0010761	abnormal microglial cell chemotaxis		IAGP		N	RGD:5509061	20220901	MGI			PMID:32241915
1556958	Hira	histone cell cycle regulator	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20141003	MGI			
1556958	Hira	histone cell cycle regulator	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884347
1556958	Hira	histone cell cycle regulator	gene	MP:0001684	abnormal axial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0003345	decreased rib number		IEA		N	RGD:5509061	20160804	MGI			
1556958	Hira	histone cell cycle regulator	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0004096	abnormal midbrain-hindbrain boundary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0004387	abnormal prechordal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250911	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884347
1556958	Hira	histone cell cycle regulator	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556958	Hira	histone cell cycle regulator	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20170216	MGI			PMID:26935106
1556958	Hira	histone cell cycle regulator	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884616
1556960	Zfp609	zinc finger protein 609	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1556960	Zfp609	zinc finger protein 609	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20200402	MGI			
1556960	Zfp609	zinc finger protein 609	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1556960	Zfp609	zinc finger protein 609	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20200402	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20231207	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0005542	cornea vascularization		IEA		N	RGD:5509061	20231207	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0005575	increased pulmonary ventilation		IEA		N	RGD:5509061	20210128	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0005586	decreased tidal volume		IEA		N	RGD:5509061	20260402	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20231207	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1556961	Nadsyn1	NAD synthetase 1	gene	MP:0010570	prolonged ST segment		IEA		N	RGD:5509061	20211021	MGI			
1556962	Ms4a8a	membrane-spanning 4-domains, subfamily A, member 8A	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1556962	Ms4a8a	membrane-spanning 4-domains, subfamily A, member 8A	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1556962	Ms4a8a	membrane-spanning 4-domains, subfamily A, member 8A	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1556965	Atg5	autophagy related 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0000639	abnormal adrenal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701890
1556965	Atg5	autophagy related 5	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479732
1556965	Atg5	autophagy related 5	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21493778
1556965	Atg5	autophagy related 5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1556965	Atg5	autophagy related 5	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626506
1556965	Atg5	autophagy related 5	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701890
1556965	Atg5	autophagy related 5	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20160728	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1556965	Atg5	autophagy related 5	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23479732
1556965	Atg5	autophagy related 5	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:20577052
1556965	Atg5	autophagy related 5	gene	MP:0003143	enlarged otoliths		IAGP		N	RGD:5509061	20141003	MGI			PMID:20577052
1556965	Atg5	autophagy related 5	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1556965	Atg5	autophagy related 5	gene	MP:0003311	aminoaciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:21493778
1556965	Atg5	autophagy related 5	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20230119	MGI			PMID:35982178
1556965	Atg5	autophagy related 5	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20230119	MGI			PMID:35982178
1556965	Atg5	autophagy related 5	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24185898
1556965	Atg5	autophagy related 5	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20160728	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701890
1556965	Atg5	autophagy related 5	gene	MP:0003897	abnormal ST segment duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525940
1556965	Atg5	autophagy related 5	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21493778
1556965	Atg5	autophagy related 5	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20160728	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21493778
1556965	Atg5	autophagy related 5	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18849966
1556965	Atg5	autophagy related 5	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20160728	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525940
1556965	Atg5	autophagy related 5	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20160728	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20180503	MGI			PMID:29438013
1556965	Atg5	autophagy related 5	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525940
1556965	Atg5	autophagy related 5	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525940
1556965	Atg5	autophagy related 5	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24209762
1556965	Atg5	autophagy related 5	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20577052
1556965	Atg5	autophagy related 5	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20160728	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160728	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20160728	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870125
1556965	Atg5	autophagy related 5	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20160811	MGI			PMID:25585051
1556965	Atg5	autophagy related 5	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525940
1556965	Atg5	autophagy related 5	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17450150
1556965	Atg5	autophagy related 5	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200917	MGI			PMID:30874544
1556965	Atg5	autophagy related 5	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0009837	abnormal sperm end piece morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0009974	decreased cerebral cortex pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625204
1556965	Atg5	autophagy related 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23426372
1556965	Atg5	autophagy related 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15525940
1556965	Atg5	autophagy related 5	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18701890
1556965	Atg5	autophagy related 5	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20160728	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870125
1556965	Atg5	autophagy related 5	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870125
1556965	Atg5	autophagy related 5	gene	MP:0014684	impaired spermiation		IAGP		N	RGD:5509061	20250703	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0020406	hyperthreoninuria		IAGP		N	RGD:5509061	20161208	MGI			PMID:21493778
1556965	Atg5	autophagy related 5	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0030591	absent sperm fibrous sheath		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0030618	tryptophanuria		IAGP		N	RGD:5509061	20180906	MGI			PMID:21493778
1556965	Atg5	autophagy related 5	gene	MP:0030620	valinuria		IAGP		N	RGD:5509061	20180920	MGI			PMID:21493778
1556965	Atg5	autophagy related 5	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20190711	MGI			PMID:18701890
1556965	Atg5	autophagy related 5	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20190711	MGI			PMID:29438013
1556965	Atg5	autophagy related 5	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:18849966
1556965	Atg5	autophagy related 5	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:21493778
1556965	Atg5	autophagy related 5	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:23479732
1556965	Atg5	autophagy related 5	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:23615463
1556965	Atg5	autophagy related 5	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220310	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0031372	abnormal sperm individualization		IAGP		N	RGD:5509061	20220331	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0031409	double-headed sperm		IAGP		N	RGD:5509061	20220630	MGI			PMID:32677505
1556965	Atg5	autophagy related 5	gene	MP:0031641	alaninuria		IAGP		N	RGD:5509061	20240801	MGI			PMID:21493778
1556966	Vmn1r51	vomeronasal 1 receptor 51	gene	MP:0009945	abnormal accessory olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11222144
1556967	St6gal2	beta galactoside alpha 2,6 sialyltransferase 2	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20211021	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20241121	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20241121	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20250508	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20250508	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20250508	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20241121	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1556968	Jade3	jade family PHD finger 3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1556969	Astl	astacin like metalloendopeptidase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22206759
1556969	Astl	astacin like metalloendopeptidase	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22472438
1556969	Astl	astacin like metalloendopeptidase	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22472438
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658188
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23893895
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23893895
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20231207	MGI			
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23893895
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23893895
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20231207	MGI			
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658188
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20231207	MGI			
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658188
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658188
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23893895
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:23893895
1556970	Mpp3	membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3)	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:23893895
1556972	Jmy	junction-mediating and regulatory protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210805	MGI			PMID:32279424
1556972	Jmy	junction-mediating and regulatory protein	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20210805	MGI			PMID:32279424
1556972	Jmy	junction-mediating and regulatory protein	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20210805	MGI			PMID:32279424
1556972	Jmy	junction-mediating and regulatory protein	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210805	MGI			PMID:32279424
1556972	Jmy	junction-mediating and regulatory protein	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210805	MGI			PMID:32279424
1556972	Jmy	junction-mediating and regulatory protein	gene	MP:0009233	enlarged sperm head		IAGP		N	RGD:5509061	20210805	MGI			PMID:32279424
1556972	Jmy	junction-mediating and regulatory protein	gene	MP:0020356	abnormal Sertoli cell barrier function		IAGP		N	RGD:5509061	20210805	MGI			PMID:32279424
1556972	Jmy	junction-mediating and regulatory protein	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20210805	MGI			PMID:32279424
1556974	Mroh9	maestro heat-like repeat family member 9	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20180705	MGI			PMID:24891606
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20180705	MGI			PMID:24891606
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20180705	MGI			PMID:24891606
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:32555348
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20180705	MGI			PMID:24891606
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20180705	MGI			PMID:24891606
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20180705	MGI			PMID:24891606
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20180705	MGI			PMID:24891606
1556979	Cntd1	cyclin N-terminal domain containing 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:24891606
1556980	Pcdh9	protocadherin 9	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220428	MGI			
1556980	Pcdh9	protocadherin 9	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170314	MGI			PMID:25802080
1556980	Pcdh9	protocadherin 9	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1556980	Pcdh9	protocadherin 9	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20170314	MGI			PMID:25802080
1556980	Pcdh9	protocadherin 9	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20181227	MGI			
1556980	Pcdh9	protocadherin 9	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1556980	Pcdh9	protocadherin 9	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1556980	Pcdh9	protocadherin 9	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20170314	MGI			PMID:25802080
1556980	Pcdh9	protocadherin 9	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20170314	MGI			PMID:25802080
1556980	Pcdh9	protocadherin 9	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20170314	MGI			PMID:25802080
1556980	Pcdh9	protocadherin 9	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20170314	MGI			PMID:25802080
1556980	Pcdh9	protocadherin 9	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1556980	Pcdh9	protocadherin 9	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1556980	Pcdh9	protocadherin 9	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:25802080
1556980	Pcdh9	protocadherin 9	gene	MP:0020396	abnormal social recognition		IAGP		N	RGD:5509061	20170314	MGI			PMID:25802080
1556980	Pcdh9	protocadherin 9	gene	MP:0021019	increased dendritic spine number		IAGP		N	RGD:5509061	20211014	MGI			PMID:25802080
1556980	Pcdh9	protocadherin 9	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25802080
1556981	Cd27	CD27 antigen	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723067
1556981	Cd27	CD27 antigen	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230601	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20241121	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062504
1556981	Cd27	CD27 antigen	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23547099
1556981	Cd27	CD27 antigen	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062504
1556981	Cd27	CD27 antigen	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723067
1556981	Cd27	CD27 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11062504
1556981	Cd27	CD27 antigen	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23547099
1556981	Cd27	CD27 antigen	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1556981	Cd27	CD27 antigen	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20230601	MGI			
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0008152	decreased diameter of femur		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0008638	increased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0030439	decreased osteoblast proliferation		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0030985	decreased circulating osteocalcin level		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556984	Itln1	intelectin 1 (galactofuranose binding)	gene	MP:0031074	increased circulating type I collagen C-terminal telopeptide level		IAGP		N	RGD:5509061	20201210	MGI			PMID:29619269
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0000396	increased curvature of hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0001280	loss of vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20170105	MGI			
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:23884312
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0008538	decreased zigzag hair amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0009351	thin hair shaft		IEA		N	RGD:5509061	20151126	MGI			
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0009441	delayed skin barrier formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0009801	abnormal hair cortex keratinization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22496784
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0010099	abnormal thoracic cage shape		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556985	Tgm3	transglutaminase 3, E polypeptide	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20151126	MGI			PMID:3711636
1556988	Padi6	peptidyl arginine deiminase, type VI	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17587491
1556988	Padi6	peptidyl arginine deiminase, type VI	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599511
1556988	Padi6	peptidyl arginine deiminase, type VI	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599511
1556988	Padi6	peptidyl arginine deiminase, type VI	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17587491
1556988	Padi6	peptidyl arginine deiminase, type VI	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20141003	MGI			PMID:17587491
1556988	Padi6	peptidyl arginine deiminase, type VI	gene	MP:0005630	increased lung weight		IEA		N	RGD:5509061	20241121	MGI			
1556992	Gjb4	gap junction protein, beta 4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20181227	MGI			
1556992	Gjb4	gap junction protein, beta 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1556992	Gjb4	gap junction protein, beta 4	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20181227	MGI			
1556992	Gjb4	gap junction protein, beta 4	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1556992	Gjb4	gap junction protein, beta 4	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210520	MGI			
1556992	Gjb4	gap junction protein, beta 4	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728008
1556992	Gjb4	gap junction protein, beta 4	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20170105	MGI			
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20161110	MGI			PMID:26662512
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20180712	MGI			PMID:27660326
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24135232
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084280
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20161110	MGI			PMID:26662512
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24135232
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:27660326
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26662512
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20161110	MGI			PMID:26662512
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0004536	short inner hair cell stereocilia		IAGP		N	RGD:5509061	20161110	MGI			PMID:26662512
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18084280
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20161110	MGI			PMID:26662512
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20161110	MGI			PMID:26662512
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0011060	abnormal kinocilium morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:24135232
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20161110	MGI			PMID:26662512
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20180712	MGI			PMID:27660326
1556993	Gpsm2	G-protein signalling modulator 2 (AGS3-like, C. elegans)	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:24135232
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0000126	brittle teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0000387	disorganized inner root sheath cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0001282	short vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0002577	reduced enamel thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0002817	abnormal tooth mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0003053	delayed tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0003930	abnormal tooth hard tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20171228	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0006369	supernumerary incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0010685	abnormal hair follicle inner root sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0010747	abnormal enamel organ morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0010773	supernumerary molars		IAGP		N	RGD:5509061	20171228	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0013129	abnormal tooth color		IAGP		N	RGD:5509061	20171221	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20260402	MGI			
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0030079	small incisors		IAGP		N	RGD:5509061	20171228	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0030088	microdontia		IAGP		N	RGD:5509061	20171228	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:18156176
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0030472	fused teeth		IAGP		N	RGD:5509061	20171228	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0030473	fused molars		IAGP		N	RGD:5509061	20171228	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0030497	short tooth root		IAGP		N	RGD:5509061	20171228	MGI			PMID:18297738
1556994	Sp6	trans-acting transcription factor 6	gene	MP:0030525	abnormal Hertwig epithelial root sheath morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:18297738
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20241121	MGI			
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20241121	MGI			
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20180118	MGI			PMID:22801574
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20241121	MGI			
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20180118	MGI			PMID:22801574
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0002436	abnormal CD8-positive, alpha-beta cytotoxic T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618603
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20180118	MGI			PMID:22801574
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20241121	MGI			
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618603
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618603
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618603
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618603
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618603
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16618603
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20241121	MGI			
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0012191	decreased cytotoxic T cell apoptosis		IAGP		N	RGD:5509061	20180118	MGI			PMID:22801574
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0013771	decreased effector memory T-helper cell number		IEA		N	RGD:5509061	20241121	MGI			
1556995	Serpinb9	serine (or cysteine) peptidase inhibitor, clade B, member 9	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16618603
1556997	Zfp524	zinc finger protein 524	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1556997	Zfp524	zinc finger protein 524	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20210617	MGI			PMID:25376646
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:25376646
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210826	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001714	absent trophoblast giant cells		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20210617	MGI			PMID:25376646
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002282	abnormal trachea morphology		IEA		N	RGD:5509061	20210520	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20241121	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:25376646
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20231207	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20241121	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20210617	MGI			PMID:25376646
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20210617	MGI			PMID:25376646
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0012100	absent spongiotrophoblast layer		IAGP		N	RGD:5509061	20250508	MGI			PMID:28943313
1556999	Naa10	N(alpha)-acetyltransferase 10, NatA catalytic subunit	gene	MP:0030278	thick neurocranium		IAGP		N	RGD:5509061	20210617	MGI			PMID:25376646
1557001	Tpm2	tropomyosin 2, beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1557001	Tpm2	tropomyosin 2, beta	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:29510160
1557001	Tpm2	tropomyosin 2, beta	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20191114	MGI			PMID:29510160
1557001	Tpm2	tropomyosin 2, beta	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20191114	MGI			PMID:29510160
1557001	Tpm2	tropomyosin 2, beta	gene	MP:0002840	abnormal lens fiber morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:29510160
1557001	Tpm2	tropomyosin 2, beta	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260402	MGI			PMID:39201474
1557001	Tpm2	tropomyosin 2, beta	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1557001	Tpm2	tropomyosin 2, beta	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20191114	MGI			PMID:29510160
1557003	Nsun3	NOL1/NOP2/Sun domain family member 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20241003	MGI			PMID:36949224
1557003	Nsun3	NOL1/NOP2/Sun domain family member 3	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20241003	MGI			PMID:36949224
1557003	Nsun3	NOL1/NOP2/Sun domain family member 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20241003	MGI			PMID:36949224
1557003	Nsun3	NOL1/NOP2/Sun domain family member 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20241003	MGI			PMID:36949224
1557003	Nsun3	NOL1/NOP2/Sun domain family member 3	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20241003	MGI			PMID:36949224
1557003	Nsun3	NOL1/NOP2/Sun domain family member 3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20241003	MGI			PMID:36949224
1557003	Nsun3	NOL1/NOP2/Sun domain family member 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20241003	MGI			PMID:36949224
1557003	Nsun3	NOL1/NOP2/Sun domain family member 3	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20241003	MGI			PMID:36949224
1557003	Nsun3	NOL1/NOP2/Sun domain family member 3	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20241003	MGI			PMID:36949224
1557004	Egfl6	EGF-like-domain, multiple 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613833
1557004	Egfl6	EGF-like-domain, multiple 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200723	MGI			PMID:32231122
1557005	Frmd5	FERM domain containing 5	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1557005	Frmd5	FERM domain containing 5	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1557005	Frmd5	FERM domain containing 5	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20160804	MGI			
1557005	Frmd5	FERM domain containing 5	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160804	MGI			
1557005	Frmd5	FERM domain containing 5	gene	MP:0014379	decreased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0020511	decreased dendritic spine length		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0020512	abnormal dendritic mushroom spine morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0020513	abnormal dendritic stubby spine morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0020514	abnormal dendritic thin spine morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0021090	abnormal dendrite arborization pattern		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557005	Frmd5	FERM domain containing 5	gene	MP:0021112	impaired social recognition		IAGP		N	RGD:5509061	20240328	MGI			PMID:38228891
1557007	Ociad2	OCIA domain containing 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1557007	Ociad2	OCIA domain containing 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1557007	Ociad2	OCIA domain containing 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0014920	increased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0020423	abnormal mitochondrial biogenesis		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557008	Rangrf	RAN guanine nucleotide release factor	gene	MP:0030567	abnormal I band morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:35533905
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273592
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273592
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0002693	abnormal pancreas physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273592
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0003503	decreased activity of thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273592
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009174	absent pancreatic beta cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009177	decreased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009178	absent pancreatic alpha cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009181	decreased pancreatic delta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009181	decreased pancreatic delta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009191	decreased pancreatic epsilon cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273592
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0011066	abnormal renal tubule epithelial cell primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273592
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273592
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19481545
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21786021
1557009	Glis3	GLIS family zinc finger 3	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273592
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234806
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234806
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22117778
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234806
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234806
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234806
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0003894	abnormal Purkinje cell innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234806
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0003894	abnormal Purkinje cell innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20537373
1557010	Cbln1	cerebellin 1 precursor protein	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:16234806
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9303352
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0002881	long hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0003358	abnormal hypaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0004248	abnormal epaxial muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9284044
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917328
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:9284044
1557013	Fgf6	fibroblast growth factor 6	gene	MP:0030945	abnormal myoblast migration		IAGP		N	RGD:5509061	20211125	MGI			PMID:12917328
1557014	Plin5	perilipin 5	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20210930	MGI			PMID:27376234
1557014	Plin5	perilipin 5	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20210930	MGI			PMID:27376234
1557014	Plin5	perilipin 5	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20210930	MGI			PMID:27376234
1557014	Plin5	perilipin 5	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20210930	MGI			PMID:27376234
1557014	Plin5	perilipin 5	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20210930	MGI			PMID:27376234
1557014	Plin5	perilipin 5	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210930	MGI			PMID:27376234
1557014	Plin5	perilipin 5	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0010360	decreased liver free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0013243	abnormal carbohydrate metabolism		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20170720	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20210930	MGI			PMID:27376234
1557014	Plin5	perilipin 5	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0030018	increased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20210930	MGI			PMID:27376234
1557014	Plin5	perilipin 5	gene	MP:0031414	decreased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0031417	decreased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:22532565
1557014	Plin5	perilipin 5	gene	MP:0031417	decreased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:25161888
1557014	Plin5	perilipin 5	gene	MP:0031417	decreased cardiac muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:27376234
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220630	MGI			PMID:28661483
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:28661483
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:28661483
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220630	MGI			PMID:28661483
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20220630	MGI			PMID:28661483
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20220630	MGI			PMID:28661483
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220630	MGI			PMID:28661483
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:28661483
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:28661483
1557015	Zmym3	zinc finger, MYM-type 3	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:28661483
1557016	Pigf	phosphatidylinositol glycan anchor biosynthesis, class F	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1557016	Pigf	phosphatidylinositol glycan anchor biosynthesis, class F	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1557016	Pigf	phosphatidylinositol glycan anchor biosynthesis, class F	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1557016	Pigf	phosphatidylinositol glycan anchor biosynthesis, class F	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1557016	Pigf	phosphatidylinositol glycan anchor biosynthesis, class F	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1557016	Pigf	phosphatidylinositol glycan anchor biosynthesis, class F	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000030	abnormal tympanic ring morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19221194
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19221194
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0003842	abnormal metopic suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004354	absent deltoid tuberosity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004444	small supraoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004463	basisphenoid bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004506	abnormal pubis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004553	absent tracheal cartilage rings		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004553	absent tracheal cartilage rings		IAGP		N	RGD:5509061	20171214	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004603	absent vertebral arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004670	small vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0004915	abnormal Reichert's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0005226	abnormal vertebral arch development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0005227	abnormal vertebral body development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0009575	abnormal pubic symphysis morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0009660	abnormal induced retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:21737784
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19221194
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19221194
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0010827	small lung saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19221194
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19221194
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19221194
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18789316
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:19221194
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0011376	abnormal kidney corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0030120	absent retrotympanic process		IAGP		N	RGD:5509061	20171005	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0030431	wide metopic suture		IAGP		N	RGD:5509061	20171214	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0030844	abnormal pubis body morphology		IAGP		N	RGD:5509061	20181025	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0030867	small thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:17035289
1557017	Bmper	BMP-binding endothelial regulator	gene	MP:0030872	small cricoid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:17035289
1557018	Mcm7	minichromosome maintenance complex component 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1557018	Mcm7	minichromosome maintenance complex component 7	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1557018	Mcm7	minichromosome maintenance complex component 7	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1557018	Mcm7	minichromosome maintenance complex component 7	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1557018	Mcm7	minichromosome maintenance complex component 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1557018	Mcm7	minichromosome maintenance complex component 7	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1557018	Mcm7	minichromosome maintenance complex component 7	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20838603
1557019	Timd2	T cell immunoglobulin and mucin domain containing 2	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982865
1557019	Timd2	T cell immunoglobulin and mucin domain containing 2	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982865
1557019	Timd2	T cell immunoglobulin and mucin domain containing 2	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982865
1557019	Timd2	T cell immunoglobulin and mucin domain containing 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982865
1557019	Timd2	T cell immunoglobulin and mucin domain containing 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982865
1557019	Timd2	T cell immunoglobulin and mucin domain containing 2	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16982865
1557020	Itgbl1	integrin, beta-like 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20240523	MGI			
1557020	Itgbl1	integrin, beta-like 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20240523	MGI			
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0003936	abnormal reproductive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0003942	abnormal urinary system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0008999	absent anus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0009252	absent urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557021	Sestd1	SEC14 and spectrin domains 1	gene	MP:0011771	abnormal genital tubercle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23696638
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0000564	syndactyly		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0002861	abnormal tail bud morphology		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20230601	MGI			
1557022	Isyna1	myo-inositol 1-phosphate synthase A1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557024	Gusb	glucuronidase, beta	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12700165
1557024	Gusb	glucuronidase, beta	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2111021
1557024	Gusb	glucuronidase, beta	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20200310	MGI			PMID:11228259
1557024	Gusb	glucuronidase, beta	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20200310	MGI			PMID:12700165
1557024	Gusb	glucuronidase, beta	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20200310	MGI			PMID:9774663
1557024	Gusb	glucuronidase, beta	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:11228259
1557024	Gusb	glucuronidase, beta	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:12700165
1557024	Gusb	glucuronidase, beta	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20200310	MGI			PMID:9774663
1557024	Gusb	glucuronidase, beta	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:11228259
1557024	Gusb	glucuronidase, beta	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0000588	thick tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:9774663
1557024	Gusb	glucuronidase, beta	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:9774663
1557024	Gusb	glucuronidase, beta	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20111116	MGI			
1557024	Gusb	glucuronidase, beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:11228259
1557024	Gusb	glucuronidase, beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:12700165
1557024	Gusb	glucuronidase, beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200310	MGI			PMID:9774663
1557024	Gusb	glucuronidase, beta	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:11228259
1557024	Gusb	glucuronidase, beta	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:12700165
1557024	Gusb	glucuronidase, beta	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9774663
1557024	Gusb	glucuronidase, beta	gene	MP:0001783	decreased white adipose tissue amount		IEA		N	RGD:5509061	20111116	MGI			
1557024	Gusb	glucuronidase, beta	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200310	MGI			PMID:12700165
1557024	Gusb	glucuronidase, beta	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:10560917
1557024	Gusb	glucuronidase, beta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:11228259
1557024	Gusb	glucuronidase, beta	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12700165
1557024	Gusb	glucuronidase, beta	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:2111021
1557024	Gusb	glucuronidase, beta	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0002566	abnormal sexual interaction		IEA		N	RGD:5509061	20111116	MGI			
1557024	Gusb	glucuronidase, beta	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:10560917
1557024	Gusb	glucuronidase, beta	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:10560917
1557024	Gusb	glucuronidase, beta	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:11228259
1557024	Gusb	glucuronidase, beta	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2111021
1557024	Gusb	glucuronidase, beta	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:9774663
1557024	Gusb	glucuronidase, beta	gene	MP:0005060	accumulation of giant lysosomes in kidney/renal tubule cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20111116	MGI			
1557024	Gusb	glucuronidase, beta	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20200310	MGI			PMID:2111021
1557024	Gusb	glucuronidase, beta	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2111021
1557024	Gusb	glucuronidase, beta	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:12700165
1557024	Gusb	glucuronidase, beta	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:2495302
1557024	Gusb	glucuronidase, beta	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:12700165
1557024	Gusb	glucuronidase, beta	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1557024	Gusb	glucuronidase, beta	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557024	Gusb	glucuronidase, beta	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20200310	MGI			PMID:14583446
1557024	Gusb	glucuronidase, beta	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20200310	MGI			PMID:12403825
1557026	Srpx2	sushi-repeat-containing protein, X-linked 2	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20230119	MGI			
1557026	Srpx2	sushi-repeat-containing protein, X-linked 2	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20180906	MGI			PMID:29920554
1557026	Srpx2	sushi-repeat-containing protein, X-linked 2	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20180906	MGI			PMID:29920554
1557026	Srpx2	sushi-repeat-containing protein, X-linked 2	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20180906	MGI			PMID:29920554
1557027	Mug1	murinoglobulin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487856
1557027	Mug1	murinoglobulin 1	gene	MP:0001657	abnormal induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487856
1557027	Mug1	murinoglobulin 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487856
1557027	Mug1	murinoglobulin 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0008054	abnormal uterine NK cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487856
1557027	Mug1	murinoglobulin 1	gene	MP:0008806	increased circulating amylase level		IAGP		N	RGD:5509061	20150611	MGI			PMID:10487856
1557027	Mug1	murinoglobulin 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10487856
1557027	Mug1	murinoglobulin 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557027	Mug1	murinoglobulin 1	gene	MP:0011886	increased circulating lipase level		IAGP		N	RGD:5509061	20150611	MGI			PMID:10487856
1557027	Mug1	murinoglobulin 1	gene	MP:0012726	abnormal uterine spiral artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14580373
1557028	Mrpl12	mitochondrial ribosomal protein L12	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1557028	Mrpl12	mitochondrial ribosomal protein L12	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20220519	MGI			
1557028	Mrpl12	mitochondrial ribosomal protein L12	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:37182101
1557028	Mrpl12	mitochondrial ribosomal protein L12	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:37182101
1557028	Mrpl12	mitochondrial ribosomal protein L12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1557028	Mrpl12	mitochondrial ribosomal protein L12	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20240620	MGI			PMID:37182101
1557028	Mrpl12	mitochondrial ribosomal protein L12	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:37182101
1557028	Mrpl12	mitochondrial ribosomal protein L12	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557029	Tulp4	TUB like protein 4	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210128	MGI			
1557029	Tulp4	TUB like protein 4	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0004175	telangiectasia		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0004665	abnormal stapedial artery morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0004880	lung cyst		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0009455	enhanced cued conditioning behavior		IEA		N	RGD:5509061	20240523	MGI			
1557029	Tulp4	TUB like protein 4	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1557029	Tulp4	TUB like protein 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0011513	abnormal vertebral artery morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0011683	dual inferior vena cava		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013162	abnormal thyroid gland isthmus morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013814	abnormal hepatic portal vein connection		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013834	thin hypoglossal nerve		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013840	absent segment of posterior cerebral artery		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013876	absent ductus venosus valve		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013936	abnormal thymus topology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013952	retroesophageal left subclavian artery		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013966	abnormal infrahyoid muscle morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013970	absent connection between subcutaneous lymph vessels and lymph sac		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013973	abnormal hepatic vein connection		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0013995	abnormal external carotid artery origin		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557029	Tulp4	TUB like protein 4	gene	MP:0020824	abnormal testis tissue architecture		IAGP		N	RGD:5509061	20240215	MGI			PMID:38115643
1557030	Magix	MAGI family member, X-linked	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1557030	Magix	MAGI family member, X-linked	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230119	MGI			
1557030	Magix	MAGI family member, X-linked	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20230119	MGI			
1557030	Magix	MAGI family member, X-linked	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20230119	MGI			
1557030	Magix	MAGI family member, X-linked	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20230119	MGI			
1557031	Septin6	septin 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16314519
1557031	Septin6	septin 6	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1557032	Tm9sf3	transmembrane 9 superfamily member 3	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1557032	Tm9sf3	transmembrane 9 superfamily member 3	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1557032	Tm9sf3	transmembrane 9 superfamily member 3	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1557032	Tm9sf3	transmembrane 9 superfamily member 3	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201231	MGI			
1557032	Tm9sf3	transmembrane 9 superfamily member 3	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1557032	Tm9sf3	transmembrane 9 superfamily member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557033	Fundc1	FUN14 domain containing 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1557033	Fundc1	FUN14 domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1557033	Fundc1	FUN14 domain containing 1	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1557033	Fundc1	FUN14 domain containing 1	gene	MP:0011942	decreased fluid intake		IEA		N	RGD:5509061	20260402	MGI			
1557035	Acod1	aconitate decarboxylase 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27189937
1557035	Acod1	aconitate decarboxylase 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0000202	abnormal circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0000613	abnormal salivary gland morphology		IEA		N	RGD:5509061	20210520	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344385
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344385
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20260402	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344385
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18495893
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20190228	MGI			PMID:25437547
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20200514	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022372
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002572	abnormal emotion/affect behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002581	abnormal ileum morphology		IEA		N	RGD:5509061	20210520	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002710	increased glucagon secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022372
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002918	abnormal paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344385
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344385
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0003271	abnormal duodenum morphology		IEA		N	RGD:5509061	20210520	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0004002	abnormal jejunum morphology		IEA		N	RGD:5509061	20210520	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022372
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022372
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21040848
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0005445	abnormal neurotransmitter secretion		IAGP		N	RGD:5509061	20190228	MGI			PMID:25437547
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:17380209
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344385
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0008953	abnormal pancreatic somatostatin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344385
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344385
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18177725
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0011267	abnormal excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:18022372
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0014647	decreased horizontal optokinetic reflex		IAGP		N	RGD:5509061	20250306	MGI			PMID:17344385
1557036	Cadps2	Ca2+-dependent activator protein for secretion 2	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:17380209
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20201022	MGI			
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20201022	MGI			
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20201022	MGI			
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20201022	MGI			
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962847
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962847
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962847
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20201022	MGI			
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20241121	MGI			
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962847
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20201022	MGI			
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962847
1557038	Rlim	ring finger protein, LIM domain interacting	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962847
1557039	Parp11	poly (ADP-ribose) polymerase family, member 11	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20161020	MGI			PMID:25673562
1557039	Parp11	poly (ADP-ribose) polymerase family, member 11	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20161020	MGI			PMID:25673562
1557039	Parp11	poly (ADP-ribose) polymerase family, member 11	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20161020	MGI			PMID:25673562
1557039	Parp11	poly (ADP-ribose) polymerase family, member 11	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1557039	Parp11	poly (ADP-ribose) polymerase family, member 11	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20161020	MGI			PMID:25673562
1557039	Parp11	poly (ADP-ribose) polymerase family, member 11	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:25673562
1557039	Parp11	poly (ADP-ribose) polymerase family, member 11	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:25673562
1557039	Parp11	poly (ADP-ribose) polymerase family, member 11	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:25673562
1557039	Parp11	poly (ADP-ribose) polymerase family, member 11	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20161020	MGI			PMID:25673562
1557041	Crebzf	CREB/ATF bZIP transcription factor	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001324	abnormal eye pigmentation		IEA		N	RGD:5509061	20160804	MGI			
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0001973	increased thermal nociceptive threshold		IEA		N	RGD:5509061	20160804	MGI			
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20169082
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20169082
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20169082
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20180201	MGI			PMID:12361980
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20180201	MGI			PMID:12361980
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0005000	abnormal immune tolerance		IAGP		N	RGD:5509061	20180201	MGI			PMID:2464645
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0005205	abnormal eye anterior chamber morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20180201	MGI			PMID:15308121
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20180201	MGI			PMID:15308121
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0008457	abnormal cortical intermediate zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:20169082
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0009332	abnormal splenocyte morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15308121
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21947081
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0012538	persistent hyaloid artery		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:20107607
1557042	Mcph1	microcephaly, primary autosomal recessive 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:20107607
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15485634
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0002619	abnormal lymphocyte morphology		IEA		N	RGD:5509061	20190418	MGI			
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:15368291
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15368291
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008082	increased single-positive T cell number		IEA		N	RGD:5509061	20150507	MGI			
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008175	absent follicular B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11509691
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18313334
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18624351
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008214	increased immature B cell number		IEA		N	RGD:5509061	20111116	MGI			
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11520463
1557043	Tnfsf13b	tumor necrosis factor (ligand) superfamily, member 13b	gene	MP:0020154	impaired humoral immune response		IEA		N	RGD:5509061	20150507	MGI			
1557044	Cpsf6	cleavage and polyadenylation specific factor 6	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20240502	MGI			PMID:38416782
1557044	Cpsf6	cleavage and polyadenylation specific factor 6	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20240502	MGI			PMID:38416782
1557044	Cpsf6	cleavage and polyadenylation specific factor 6	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20240502	MGI			PMID:38416782
1557044	Cpsf6	cleavage and polyadenylation specific factor 6	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20240502	MGI			PMID:38416782
1557045	Acnat2	acyl-coenzyme A amino acid N-acyltransferase 2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1557045	Acnat2	acyl-coenzyme A amino acid N-acyltransferase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1557048	Gprasp3	G protein-coupled receptor associated sorting protein family member 3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20240620	MGI			PMID:37890669
1557048	Gprasp3	G protein-coupled receptor associated sorting protein family member 3	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20240620	MGI			PMID:37890669
1557048	Gprasp3	G protein-coupled receptor associated sorting protein family member 3	gene	MP:0014473	increased pulmonary alveolus wall thickness		IAGP		N	RGD:5509061	20240704	MGI			PMID:37890669
1557048	Gprasp3	G protein-coupled receptor associated sorting protein family member 3	gene	MP:0031632	increased lung cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:37890669
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0009455	enhanced cued conditioning behavior		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0020852	abnormal olfactory behavior		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557049	Slitrk4	SLIT and NTRK-like family, member 4	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20240808	MGI			PMID:38736483
1557050	Dcp1a	decapping mRNA 1A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20210603	MGI			PMID:33813271
1557050	Dcp1a	decapping mRNA 1A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20210603	MGI			PMID:33813271
1557050	Dcp1a	decapping mRNA 1A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210603	MGI			PMID:33813271
1557050	Dcp1a	decapping mRNA 1A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210603	MGI			PMID:33813271
1557051	Lancl3	LanC lantibiotic synthetase component C-like 3 (bacterial)	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220519	MGI			
1557051	Lancl3	LanC lantibiotic synthetase component C-like 3 (bacterial)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240222	MGI			PMID:33932340
1557051	Lancl3	LanC lantibiotic synthetase component C-like 3 (bacterial)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180222	MGI			PMID:28106097
1557051	Lancl3	LanC lantibiotic synthetase component C-like 3 (bacterial)	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20220519	MGI			
1557053	Ahrr	aryl-hydrocarbon receptor repressor	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210826	MGI			
1557053	Ahrr	aryl-hydrocarbon receptor repressor	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1557053	Ahrr	aryl-hydrocarbon receptor repressor	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18022386
1557053	Ahrr	aryl-hydrocarbon receptor repressor	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20241121	MGI			
1557053	Ahrr	aryl-hydrocarbon receptor repressor	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
1557053	Ahrr	aryl-hydrocarbon receptor repressor	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210520	MGI			
1557053	Ahrr	aryl-hydrocarbon receptor repressor	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20210520	MGI			
1557055	Odad4	outer dynein arm complex subunit 4	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20180201	MGI			PMID:27486780
1557055	Odad4	outer dynein arm complex subunit 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:27486780
1557055	Odad4	outer dynein arm complex subunit 4	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:27486780
1557055	Odad4	outer dynein arm complex subunit 4	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20180201	MGI			PMID:27486780
1557055	Odad4	outer dynein arm complex subunit 4	gene	MP:0010752	impaired mucociliary clearance		IAGP		N	RGD:5509061	20180201	MGI			PMID:27486780
1557055	Odad4	outer dynein arm complex subunit 4	gene	MP:0010854	lung situs inversus		IAGP		N	RGD:5509061	20180201	MGI			PMID:27486780
1557055	Odad4	outer dynein arm complex subunit 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:27486780
1557055	Odad4	outer dynein arm complex subunit 4	gene	MP:0012093	absent nodal flow		IAGP		N	RGD:5509061	20180201	MGI			PMID:27486780
1557058	Myo18b	myosin XVIIIb	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1557058	Myo18b	myosin XVIIIb	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18761673
1557058	Myo18b	myosin XVIIIb	gene	MP:0004062	dilated heart right atrium		IAGP		N	RGD:5509061	20231221	MGI			PMID:18761673
1557058	Myo18b	myosin XVIIIb	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1557058	Myo18b	myosin XVIIIb	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18761673
1557058	Myo18b	myosin XVIIIb	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18761673
1557058	Myo18b	myosin XVIIIb	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18761673
1557058	Myo18b	myosin XVIIIb	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18761673
1557058	Myo18b	myosin XVIIIb	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557058	Myo18b	myosin XVIIIb	gene	MP:0031613	fetal cardiomyocyte disarray		IAGP		N	RGD:5509061	20240321	MGI			PMID:18761673
1557059	Tspyl2	TSPY-like 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557059	Tspyl2	TSPY-like 2	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20141003	MGI			PMID:21738728
1557059	Tspyl2	TSPY-like 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220811	MGI			
1557061	Zcchc17	zinc finger, CCHC domain containing 17	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20230119	MGI			
1557061	Zcchc17	zinc finger, CCHC domain containing 17	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230119	MGI			
1557061	Zcchc17	zinc finger, CCHC domain containing 17	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20180412	MGI			PMID:26721440
1557061	Zcchc17	zinc finger, CCHC domain containing 17	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230119	MGI			
1557061	Zcchc17	zinc finger, CCHC domain containing 17	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20180412	MGI			PMID:26721440
1557061	Zcchc17	zinc finger, CCHC domain containing 17	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20180412	MGI			PMID:26721440
1557062	Pcbp1	poly(rC) binding protein 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1557062	Pcbp1	poly(rC) binding protein 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1557062	Pcbp1	poly(rC) binding protein 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1557062	Pcbp1	poly(rC) binding protein 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170928	MGI			PMID:26527618
1557063	Mier1	MEIR1 treanscription regulator	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20160804	MGI			
1557063	Mier1	MEIR1 treanscription regulator	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1557063	Mier1	MEIR1 treanscription regulator	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20160804	MGI			
1557063	Mier1	MEIR1 treanscription regulator	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20160804	MGI			
1557063	Mier1	MEIR1 treanscription regulator	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1557063	Mier1	MEIR1 treanscription regulator	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1557063	Mier1	MEIR1 treanscription regulator	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1557064	Fuom	fucose mutarotase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20609214
1557064	Fuom	fucose mutarotase	gene	MP:0001376	abnormal mating receptivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20609214
1557064	Fuom	fucose mutarotase	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20609214
1557064	Fuom	fucose mutarotase	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1557064	Fuom	fucose mutarotase	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20609214
1557064	Fuom	fucose mutarotase	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20609214
1557064	Fuom	fucose mutarotase	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1557064	Fuom	fucose mutarotase	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20250508	MGI			
1557065	Cd84	CD84 antigen	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557065	Cd84	CD84 antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25551754
1557065	Cd84	CD84 antigen	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557065	Cd84	CD84 antigen	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1557065	Cd84	CD84 antigen	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557065	Cd84	CD84 antigen	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557065	Cd84	CD84 antigen	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557065	Cd84	CD84 antigen	gene	MP:0009058	decreased interleukin-21 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557065	Cd84	CD84 antigen	gene	MP:0010084	abnormal long lived plasma cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557068	Ep400	E1A binding protein p400	gene	MP:0000215	absent erythrocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535249
1557068	Ep400	E1A binding protein p400	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20610385
1557068	Ep400	E1A binding protein p400	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535249
1557068	Ep400	E1A binding protein p400	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535249
1557068	Ep400	E1A binding protein p400	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535249
1557068	Ep400	E1A binding protein p400	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20610385
1557068	Ep400	E1A binding protein p400	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20610385
1557068	Ep400	E1A binding protein p400	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535249
1557068	Ep400	E1A binding protein p400	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20610385
1557068	Ep400	E1A binding protein p400	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20610385
1557068	Ep400	E1A binding protein p400	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20610385
1557068	Ep400	E1A binding protein p400	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535249
1557068	Ep400	E1A binding protein p400	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20610385
1557068	Ep400	E1A binding protein p400	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20610385
1557068	Ep400	E1A binding protein p400	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20610385
1557068	Ep400	E1A binding protein p400	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17535249
1557068	Ep400	E1A binding protein p400	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0001602	impaired myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128773
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387740
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387740
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128773
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008101	lymph node hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008122	decreased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008122	decreased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128773
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15128773
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22615130
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387740
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387740
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10828034
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387740
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0010740	abnormal dendritic cell chemotaxis		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0013649	decreased CD11b-high dendritic cell number		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1557069	Flt3l	FMS-like tyrosine kinase 3 ligand	gene	MP:0013655	decreased CD103-positive CD11b-low dendritic cell number		IAGP		N	RGD:5509061	20150924	MGI			PMID:23168837
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:15837621
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:21156286
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:21514245
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000423	delayed hair regrowth		IAGP		N	RGD:5509061	20180719	MGI			PMID:21156286
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21514245
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21156286
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21514245
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20180719	MGI			PMID:15837621
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001231	abnormal epidermis stratum basale morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21156286
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001234	absent suprabasal layer		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180719	MGI			PMID:10071215
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180719	MGI			PMID:21156286
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180719	MGI			PMID:19383288
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:15837621
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180719	MGI			PMID:10071215
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002019	abnormal tumor incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:15837621
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:15837621
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:17299132
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:21156286
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180719	MGI			PMID:21514245
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:10071215
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:21514245
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180719	MGI			PMID:25155958
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20180719	MGI			PMID:18039844
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20180719	MGI			PMID:15837621
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20180719	MGI			PMID:21156286
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:21156286
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:24101512
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20180719	MGI			PMID:10071215
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:24101512
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20180719	MGI			PMID:15837621
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20180719	MGI			PMID:19383288
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0004882	enlarged lung		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:18039844
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:18039844
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008716	increased lung non-small cell carcinoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20180719	MGI			PMID:22431510
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:21088222
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:17468755
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20180719	MGI			PMID:20609353
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0010537	tumor regression		IAGP		N	RGD:5509061	20180719	MGI			PMID:21156286
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:10071215
1557071	Polr2a	polymerase (RNA) II (DNA directed) polypeptide A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:10837119
1557072	Sytl3	synaptotagmin-like 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1557073	Pm20d1	peptidase M20 domain containing 1	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20230119	MGI			
1557073	Pm20d1	peptidase M20 domain containing 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20230119	MGI			
1557073	Pm20d1	peptidase M20 domain containing 1	gene	MP:0001982	decreased chemically-elicited antinociception		IAGP		N	RGD:5509061	20181018	MGI			PMID:29967167
1557073	Pm20d1	peptidase M20 domain containing 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1557073	Pm20d1	peptidase M20 domain containing 1	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20181018	MGI			PMID:29967167
1557073	Pm20d1	peptidase M20 domain containing 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20181018	MGI			PMID:29967167
1557073	Pm20d1	peptidase M20 domain containing 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20181018	MGI			PMID:29967167
1557073	Pm20d1	peptidase M20 domain containing 1	gene	MP:0011019	abnormal adaptive thermogenesis		IAGP		N	RGD:5509061	20181018	MGI			PMID:29967167
1557073	Pm20d1	peptidase M20 domain containing 1	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20181018	MGI			PMID:29967167
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20221215	MGI			
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009837	abnormal sperm end piece morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0030591	absent sperm fibrous sheath		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0031351	abnormal sperm flagellum thickness		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557075	Dnah2	dynein, axonemal, heavy chain 2	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:33968937
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539900
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539900
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539900
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539900
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539900
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539900
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539900
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539900
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:18539900
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21690395
1557076	Ulk1	unc-51 like kinase 1	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260611	MGI			PMID:18539900
1557080	Ophn1	oligophrenin 1	gene	MP:0000402	abnormal zigzag hair morphology		IEA		N	RGD:5509061	20150730	MGI			
1557080	Ophn1	oligophrenin 1	gene	MP:0000410	waved hair		IEA		N	RGD:5509061	20150730	MGI			
1557080	Ophn1	oligophrenin 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20150730	MGI			
1557080	Ophn1	oligophrenin 1	gene	MP:0001274	curly vibrissae		IEA		N	RGD:5509061	20150730	MGI			
1557080	Ophn1	oligophrenin 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0001935	decreased litter size		IEA		N	RGD:5509061	20150730	MGI			
1557080	Ophn1	oligophrenin 1	gene	MP:0002061	abnormal aggression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0002675	asthenozoospermia		IEA		N	RGD:5509061	20150730	MGI			
1557080	Ophn1	oligophrenin 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17728457
1557080	Ophn1	oligophrenin 1	gene	MP:0010231	transverse fur striping		IEA		N	RGD:5509061	20150730	MGI			
1557080	Ophn1	oligophrenin 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20150730	MGI			
1557081	Ptcd3	pentatricopeptide repeat domain 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1557081	Ptcd3	pentatricopeptide repeat domain 3	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1557081	Ptcd3	pentatricopeptide repeat domain 3	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20210520	MGI			
1557081	Ptcd3	pentatricopeptide repeat domain 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557081	Ptcd3	pentatricopeptide repeat domain 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557082	Tbx10	T-box 10	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:6230750
1557082	Tbx10	T-box 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118109
1557082	Tbx10	T-box 10	gene	MP:0001394	circling		IEA		N	RGD:5509061	20111116	MGI			
1557082	Tbx10	T-box 10	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20162674
1557082	Tbx10	T-box 10	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0002939	head spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0002980	abnormal postural reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0003069	abnormal superior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0003987	small vestibular ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0004289	abnormal bony labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0004317	small vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0004336	small utricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0004427	abnormal vestibular labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0004718	abnormal vestibular nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0006409	vestibular ganglion hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0009265	delayed eyelid fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118109
1557082	Tbx10	T-box 10	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118109
1557082	Tbx10	T-box 10	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15118109
1557082	Tbx10	T-box 10	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0031447	unilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:5297683
1557082	Tbx10	T-box 10	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:15118109
1557082	Tbx10	T-box 10	gene	MP:0031448	bilateral cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:5297683
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001038	abnormal cholinergic neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20180201	MGI			PMID:18931664
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20180201	MGI			PMID:17478722
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20180201	MGI			PMID:18931664
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20180201	MGI			PMID:17478722
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20180201	MGI			PMID:18931664
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0001908	abnormal somatosensory cortex physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:14687544
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:17478722
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:18931664
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:26931567
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:14687544
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:10818140
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002801	abnormal long-term object recognition memory		IAGP		N	RGD:5509061	20180201	MGI			PMID:17478722
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17478722
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20180201	MGI			PMID:17478722
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20180201	MGI			PMID:17478722
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20180201	MGI			PMID:18562603
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:10818140
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:14687544
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:15502844
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:17478722
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:18562603
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:22492035
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20180201	MGI			PMID:25741723
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:14687544
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0004254	cerebral amyloid angiopathy		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0006203	eye hemorrhage		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0008287	abnormal subiculum morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:14687544
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15502844
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0008569	lethality at weaning		IAGP		N	RGD:5509061	20180201	MGI			PMID:26931567
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0009026	abnormal brain pia mater morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21088218
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:17478722
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17360894
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:26931567
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:26931567
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20151112	MGI			PMID:22689450
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240912	MGI			PMID:34156424
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0014573	increased circulating resistin level		IAGP		N	RGD:5509061	20241128	MGI			PMID:19273596
1557085	Zbtb20	zinc finger and BTB domain containing 20	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20180201	MGI			PMID:18562603
1557086	Slc44a4	solute carrier family 44, member 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240808	MGI			PMID:38713615
1557086	Slc44a4	solute carrier family 44, member 4	gene	MP:0001671	abnormal vitamin absorption		IAGP		N	RGD:5509061	20240808	MGI			PMID:38713615
1557086	Slc44a4	solute carrier family 44, member 4	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1557086	Slc44a4	solute carrier family 44, member 4	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20240808	MGI			PMID:38713615
1557086	Slc44a4	solute carrier family 44, member 4	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1557086	Slc44a4	solute carrier family 44, member 4	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1557086	Slc44a4	solute carrier family 44, member 4	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20240808	MGI			PMID:38713615
1557088	Qrfprl	pyroglutamylated RFamide peptide receptor like	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20250102	MGI			PMID:36251705
1557089	Plin3	perilipin 3	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0009116	abnormal brown fat cell morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0020426	abnormal beige fat cell physiology		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557089	Plin3	perilipin 3	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20180607	MGI			PMID:29440067
1557090	Msl3	MSL complex subunit 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1557091	Galnt17	polypeptide N-acetylgalactosaminyltransferase 17	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210805	MGI			
1557092	Klrb1b	killer cell lectin-like receptor subfamily B member 1B	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20200310	MGI			PMID:25612621
1557092	Klrb1b	killer cell lectin-like receptor subfamily B member 1B	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25612621
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230601	MGI			
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223988
1557093	Lgr6	leucine-rich repeat-containing G protein-coupled receptor 6	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1557094	Vsig1	V-set and immunoglobulin domain containing 1	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21991385
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21325512
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21325512
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21325512
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:21325512
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21325512
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0011854	cerebral edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22820399
1557097	Srgap3	SLIT-ROBO Rho GTPase activating protein 3	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:21325512
1557098	Tfap2e	transcription factor AP-2, epsilon	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19580868
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000031	abnormal cochlea morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27162350
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000158	absent sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20170216	MGI			PMID:27162350
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230601	MGI			
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20170216	MGI			PMID:27162350
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27162350
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230601	MGI			
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20170216	MGI			PMID:27162350
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0004256	abnormal maternal decidual layer morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0009284	abnormal sympathetic neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20170216	MGI			PMID:27162350
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27162350
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0009575	abnormal pubic symphysis morphology		IAGP		N	RGD:5509061	20181018	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0009666	abnormal embryo attachment		IAGP		N	RGD:5509061	20170622	MGI			PMID:25043182
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20230601	MGI			
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713269
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343533
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20170216	MGI			PMID:27162350
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20240405	MGI			PMID:27162350
1557099	Ror1	receptor tyrosine kinase-like orphan receptor 1	gene	MP:0020359	abnormal ribbon synapse morphology		IAGP		N	RGD:5509061	20170216	MGI			PMID:27162350
1557100	Pex26	peroxisomal biogenesis factor 26	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20160811	MGI			
1557100	Pex26	peroxisomal biogenesis factor 26	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20170105	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20181227	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20181227	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0000706	small thymus		IEA		N	RGD:5509061	20181227	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20181227	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0012286	decreased frequency of paradoxical sleep		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0012292	decreased slow-wave sleep duration		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20241121	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0014639	decreased sleep duration		IAGP		N	RGD:5509061	20250306	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0020422	decreased freezing behavior		IEA		N	RGD:5509061	20210128	MGI			
1557102	Upf3b	UPF3 regulator of nonsense transcripts homolog B (yeast)	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20180201	MGI			PMID:28948974
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0012436	increased colon tumor incidence		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557103	Tnfaip8l1	tumor necrosis factor, alpha-induced protein 8-like 1	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20240111	MGI			PMID:37459052
1557104	Tuba3b	tubulin, alpha 3B	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20211021	MGI			PMID:34326397
1557104	Tuba3b	tubulin, alpha 3B	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20211021	MGI			PMID:34326397
1557104	Tuba3b	tubulin, alpha 3B	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20211021	MGI			PMID:34326397
1557105	Foxk1	forkhead box K1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446708
1557105	Foxk1	forkhead box K1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
1557105	Foxk1	forkhead box K1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
1557105	Foxk1	forkhead box K1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
1557105	Foxk1	forkhead box K1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
1557105	Foxk1	forkhead box K1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12446708
1557105	Foxk1	forkhead box K1	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
1557105	Foxk1	forkhead box K1	gene	MP:0005571	decreased lactate dehydrogenase level		IAGP		N	RGD:5509061	20250227	MGI			PMID:30700909
1557105	Foxk1	forkhead box K1	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
1557105	Foxk1	forkhead box K1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10792059
1557105	Foxk1	forkhead box K1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20250227	MGI			PMID:30700909
1557105	Foxk1	forkhead box K1	gene	MP:0012185	abnormal muscle precursor cell morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:12446708
1557105	Foxk1	forkhead box K1	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:10792059
1557105	Foxk1	forkhead box K1	gene	MP:0014449	decreased enzyme/coenzyme level		IAGP		N	RGD:5509061	20250227	MGI			PMID:30700909
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023867
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023867
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023867
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20230518	MGI			PMID:32086523
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20230518	MGI			PMID:32086523
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11023867
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0010767	abnormal female meiosis I arrest		IAGP		N	RGD:5509061	20230518	MGI			PMID:32086523
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0011122	absent primordial ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:11023867
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0013507	increased ovary apoptosis		IAGP		N	RGD:5509061	20230518	MGI			PMID:32086523
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:32086523
1557106	Figla	folliculogenesis specific basic helix-loop-helix	gene	MP:0031474	increased female germ cell apoptosis		IAGP		N	RGD:5509061	20230615	MGI			PMID:32086523
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0001800	abnormal humoral immune response		IEA		N	RGD:5509061	20200310	MGI			
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200310	MGI			PMID:9653162
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776904
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776905
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776907
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776907
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776905
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776907
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:15729333
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:9653162
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776907
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776907
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776904
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776905
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776907
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21435585
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23315079
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23481257
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:9653162
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008077	abnormal CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776904
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776905
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776907
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23315079
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:9653162
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776907
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23481257
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776905
1557107	Zbtb7b	zinc finger and BTB domain containing 7B	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:18776905
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0000826	abnormal third ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24076219
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001317	abnormal pupil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001333	absent optic nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0002697	abnormal eye size		IEA		N	RGD:5509061	20160804	MGI			
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0003671	abnormal eyelid aperture		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:24076219
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0004609	vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0006241	abnormal placement of pupils		IEA		N	RGD:5509061	20160804	MGI			
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:24076219
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008391	abnormal primordial germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20150122	MGI			PMID:22922648
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20170601	MGI			PMID:26980188
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24076219
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150122	MGI			PMID:22922648
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0010102	increased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0010207	abnormal telomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23994477
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24076219
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24076219
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21240276
1557108	Slx4	SLX4 structure-specific endonuclease subunit	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24076219
1557109	Il36g	interleukin 36G	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20201029	MGI			PMID:31578266
1557109	Il36g	interleukin 36G	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20201029	MGI			PMID:28176791
1557109	Il36g	interleukin 36G	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20201029	MGI			PMID:28176791
1557109	Il36g	interleukin 36G	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:29848754
1557109	Il36g	interleukin 36G	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:28327619
1557109	Il36g	interleukin 36G	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:28327619
1557109	Il36g	interleukin 36G	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:28327619
1557109	Il36g	interleukin 36G	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20201029	MGI			PMID:28327619
1557109	Il36g	interleukin 36G	gene	MP:0008712	decreased interleukin-9 secretion		IAGP		N	RGD:5509061	20201029	MGI			PMID:28327619
1557109	Il36g	interleukin 36G	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20201029	MGI			PMID:28176791
1557109	Il36g	interleukin 36G	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20201029	MGI			PMID:31578266
1557109	Il36g	interleukin 36G	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20201029	MGI			PMID:29848754
1557109	Il36g	interleukin 36G	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20201029	MGI			PMID:29848754
1557109	Il36g	interleukin 36G	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20201029	MGI			PMID:28176791
1557109	Il36g	interleukin 36G	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20201029	MGI			PMID:29848754
1557109	Il36g	interleukin 36G	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20201029	MGI			PMID:28176791
1557109	Il36g	interleukin 36G	gene	MP:0011080	increased macrophage apoptosis		IAGP		N	RGD:5509061	20201029	MGI			PMID:29848754
1557109	Il36g	interleukin 36G	gene	MP:0013648	increased CD11b-high dendritic cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:29848754
1557109	Il36g	interleukin 36G	gene	MP:0014229	decreased alveolar macrophage number		IAGP		N	RGD:5509061	20201029	MGI			PMID:29848754
1557109	Il36g	interleukin 36G	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20201029	MGI			PMID:31578266
1557109	Il36g	interleukin 36G	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20201029	MGI			PMID:29848754
1557109	Il36g	interleukin 36G	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20201029	MGI			PMID:31578266
1557109	Il36g	interleukin 36G	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20201029	MGI			PMID:29848754
1557110	Gar1	GAR1 ribonucleoprotein	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20160804	MGI			
1557110	Gar1	GAR1 ribonucleoprotein	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20141003	MGI			
1557110	Gar1	GAR1 ribonucleoprotein	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20141003	MGI			
1557110	Gar1	GAR1 ribonucleoprotein	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20141003	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20240523	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0000613	abnormal salivary gland morphology		IEA		N	RGD:5509061	20260402	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20240523	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20240523	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20240523	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20260402	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20240523	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20260402	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0003402	decreased liver weight		IEA		N	RGD:5509061	20241121	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0003671	abnormal eyelid aperture		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20241121	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557111	Macroh2a2	macroH2A.2 histone	gene	MP:0013745	abnormal eyelid margin morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:25312643
1557113	Icosl	icos ligand	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833154
1557113	Icosl	icos ligand	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833154
1557113	Icosl	icos ligand	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714510
1557113	Icosl	icos ligand	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714510
1557113	Icosl	icos ligand	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833154
1557113	Icosl	icos ligand	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714510
1557113	Icosl	icos ligand	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714510
1557113	Icosl	icos ligand	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833154
1557113	Icosl	icos ligand	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833154
1557113	Icosl	icos ligand	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833154
1557113	Icosl	icos ligand	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833154
1557113	Icosl	icos ligand	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12833154
1557113	Icosl	icos ligand	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714510
1557113	Icosl	icos ligand	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714510
1557113	Icosl	icos ligand	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714510
1557113	Icosl	icos ligand	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557113	Icosl	icos ligand	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714510
1557113	Icosl	icos ligand	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714510
1557113	Icosl	icos ligand	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14615582
1557114	Nrk	Nik related kinase	gene	MP:0004260	enlarged placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715335
1557114	Nrk	Nik related kinase	gene	MP:0004514	dystocia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715335
1557114	Nrk	Nik related kinase	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715335
1557114	Nrk	Nik related kinase	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715335
1557114	Nrk	Nik related kinase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715335
1557114	Nrk	Nik related kinase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715335
1557114	Nrk	Nik related kinase	gene	MP:0012098	increased spongiotrophoblast size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21715335
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098235
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098235
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0001940	testis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098235
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0003830	abnormal testis development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098235
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17098235
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:17447844
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:17098235
1557115	Dmrtc2	doublesex and mab-3 related transcription factor like family C2	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:17447844
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20160804	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0000458	abnormal mandible morphology		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20241121	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180607	MGI			PMID:28887018
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20180607	MGI			PMID:28887018
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20210520	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20241121	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28887018
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20210520	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20260402	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20180607	MGI			PMID:28887018
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20180607	MGI			PMID:28887018
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24223149
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24223149
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180607	MGI			PMID:28887018
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24223149
1557116	Dpp9	dipeptidylpeptidase 9	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20150402	MGI			PMID:24802759
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20150402	MGI			PMID:24802759
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20181227	MGI			
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20150402	MGI			PMID:24802759
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20150402	MGI			PMID:24802759
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150402	MGI			PMID:24802759
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0004905	decreased uterus weight		IAGP		N	RGD:5509061	20150402	MGI			PMID:24802759
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20150402	MGI			PMID:24802759
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20181227	MGI			
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20150402	MGI			PMID:24802759
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150402	MGI			PMID:24802759
1557118	Kdm5b	lysine demethylase 5B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557119	Tmprss11e	transmembrane protease, serine 11e	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20191031	MGI			PMID:31501243
1557120	Atp9b	ATPase, class II, type 9B	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1557120	Atp9b	ATPase, class II, type 9B	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1557122	Il22ra1	interleukin 22 receptor, alpha 1	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:24211183
1557122	Il22ra1	interleukin 22 receptor, alpha 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24211183
1557122	Il22ra1	interleukin 22 receptor, alpha 1	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1557122	Il22ra1	interleukin 22 receptor, alpha 1	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1557122	Il22ra1	interleukin 22 receptor, alpha 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1557122	Il22ra1	interleukin 22 receptor, alpha 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24211183
1557122	Il22ra1	interleukin 22 receptor, alpha 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20160804	MGI			
1557122	Il22ra1	interleukin 22 receptor, alpha 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20210617	MGI			PMID:33753942
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210826	MGI			
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20240523	MGI			
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20230601	MGI			
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20230601	MGI			
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20230601	MGI			
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047684
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047684
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21435586
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21435586
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047684
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21435586
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047684
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047684
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19047684
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0011951	increased cardiac stroke volume		IEA		N	RGD:5509061	20231207	MGI			
1557123	Rsad2	radical S-adenosyl methionine domain containing 2	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1557126	Hoxb7	homeobox B7	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784603
1557126	Hoxb7	homeobox B7	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784603
1557126	Hoxb7	homeobox B7	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784603
1557126	Hoxb7	homeobox B7	gene	MP:0012283	decreased sternebra number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784603
1557127	Tmem70	transmembrane protein 70	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20210520	MGI			
1557127	Tmem70	transmembrane protein 70	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20190502	MGI			
1557127	Tmem70	transmembrane protein 70	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1557127	Tmem70	transmembrane protein 70	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20190502	MGI			
1557127	Tmem70	transmembrane protein 70	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20190502	MGI			
1557127	Tmem70	transmembrane protein 70	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20190502	MGI			
1557127	Tmem70	transmembrane protein 70	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0003794	delayed somite formation		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557127	Tmem70	transmembrane protein 70	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0012082	delayed heart development		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0012708	delayed rostral neuropore closure		IAGP		N	RGD:5509061	20170803	MGI			PMID:28173120
1557127	Tmem70	transmembrane protein 70	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557127	Tmem70	transmembrane protein 70	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:28173120
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20171012	MGI			PMID:23267082
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0001695	abnormal gastrulation		IEA		N	RGD:5509061	20111116	MGI			
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267082
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267082
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0003821	decreased left ventricle diastolic pressure		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267082
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267082
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20201112	MGI			PMID:31634484
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:22966205
1557128	Nono	non-POU-domain-containing, octamer binding protein	gene	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:23267082
1557129	Zfp69	zinc finger protein 69	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20250508	MGI			
1557129	Zfp69	zinc finger protein 69	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20201022	MGI			
1557129	Zfp69	zinc finger protein 69	gene	MP:0004151	decreased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1557129	Zfp69	zinc finger protein 69	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20250508	MGI			
1557130	Stard3	StAR related lipid transfer domain containing 3	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14963026
1557131	Fam184b	family with sequence similarity 184, member B	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20221215	MGI			
1557131	Fam184b	family with sequence similarity 184, member B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1557131	Fam184b	family with sequence similarity 184, member B	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20210805	MGI			
1557132	Gpr75	G protein-coupled receptor 75	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20240905	MGI			PMID:36978267
1557132	Gpr75	G protein-coupled receptor 75	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20240905	MGI			PMID:36978267
1557132	Gpr75	G protein-coupled receptor 75	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20231116	MGI			PMID:37840219
1557132	Gpr75	G protein-coupled receptor 75	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:37840219
1557132	Gpr75	G protein-coupled receptor 75	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20231116	MGI			PMID:37840219
1557132	Gpr75	G protein-coupled receptor 75	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20231116	MGI			PMID:37840219
1557132	Gpr75	G protein-coupled receptor 75	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20240905	MGI			PMID:36978267
1557132	Gpr75	G protein-coupled receptor 75	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20231116	MGI			PMID:37840219
1557132	Gpr75	G protein-coupled receptor 75	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20231116	MGI			PMID:37840219
1557133	Setd6	SET domain containing 6	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1557133	Setd6	SET domain containing 6	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1557133	Setd6	SET domain containing 6	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220519	MGI			
1557133	Setd6	SET domain containing 6	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1557133	Setd6	SET domain containing 6	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1557133	Setd6	SET domain containing 6	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1557133	Setd6	SET domain containing 6	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220519	MGI			
1557133	Setd6	SET domain containing 6	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1557133	Setd6	SET domain containing 6	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20220519	MGI			
1557133	Setd6	SET domain containing 6	gene	MP:0012121	sclerocornea		IEA		N	RGD:5509061	20160421	MGI			
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0011388	absent heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0011389	absent optic disk		IAGP		N	RGD:5509061	20141003	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:21531335
1557136	Mterf4	mitochondrial transcription termination factor 4	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260716	MGI			PMID:21531335
1557137	Clec1a	C-type lectin domain family 1, member a	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20221124	MGI			PMID:35135958
1557137	Clec1a	C-type lectin domain family 1, member a	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20221124	MGI			PMID:35135958
1557137	Clec1a	C-type lectin domain family 1, member a	gene	MP:0011823	decreased CD8-positive, alpha-beta memory T cell proliferation		IAGP		N	RGD:5509061	20221124	MGI			PMID:35135958
1557138	Ctnnbl1	catenin, beta like 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20161013	MGI			PMID:23343763
1557138	Ctnnbl1	catenin, beta like 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20161013	MGI			PMID:23343763
1557138	Ctnnbl1	catenin, beta like 1	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20161013	MGI			PMID:23343763
1557138	Ctnnbl1	catenin, beta like 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:23343763
1557138	Ctnnbl1	catenin, beta like 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:23343763
1557140	Dmac2	distal membrane arm assembly complex 2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1557140	Dmac2	distal membrane arm assembly complex 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22706340
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22706340
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22706340
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9384589
1557143	Spib	Spi-B transcription factor (Spi-1/PU.1 related)	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10229183
1557144	Elavl4	ELAV like RNA binding protein 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764704
1557144	Elavl4	ELAV like RNA binding protein 4	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764704
1557144	Elavl4	ELAV like RNA binding protein 4	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764704
1557144	Elavl4	ELAV like RNA binding protein 4	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764704
1557144	Elavl4	ELAV like RNA binding protein 4	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764704
1557144	Elavl4	ELAV like RNA binding protein 4	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15764704
1557144	Elavl4	ELAV like RNA binding protein 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22998874
1557144	Elavl4	ELAV like RNA binding protein 4	gene	MP:0030737	decreased glutamic acid level		IAGP		N	RGD:5509061	20180927	MGI			PMID:22998874
1557146	Hoxc13	homeobox C13	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789037
1557146	Hoxc13	homeobox C13	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789037
1557146	Hoxc13	homeobox C13	gene	MP:0000425	loss of eyelid cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20220217	MGI			PMID:7000960
1557146	Hoxc13	homeobox C13	gene	MP:0000580	deformed nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0000580	deformed nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789037
1557146	Hoxc13	homeobox C13	gene	MP:0000582	toenail hyperkeratosis		IEA		N	RGD:5509061	20220217	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0000749	muscle degeneration		IEA		N	RGD:5509061	20220217	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0000763	abnormal filiform papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0000763	abnormal filiform papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789037
1557146	Hoxc13	homeobox C13	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:7000960
1557146	Hoxc13	homeobox C13	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20220217	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20220217	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789037
1557146	Hoxc13	homeobox C13	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20220217	MGI			PMID:21020475
1557146	Hoxc13	homeobox C13	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20220217	MGI			PMID:7000960
1557146	Hoxc13	homeobox C13	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0002981	increased liver weight		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:7000960
1557146	Hoxc13	homeobox C13	gene	MP:0003810	abnormal hair cuticle		IEA		N	RGD:5509061	20220217	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20220217	MGI			PMID:7000960
1557146	Hoxc13	homeobox C13	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0003848	brittle hair		IAGP		N	RGD:5509061	20220217	MGI			PMID:21020475
1557146	Hoxc13	homeobox C13	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0004614	caudal vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0004819	decreased skeletal muscle mass		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0008770	decreased survivor rate		IEA		N	RGD:5509061	20220217	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0010233	hairless tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9420327
1557146	Hoxc13	homeobox C13	gene	MP:0011971	increased circulating lactate dehydrogenase level		IEA		N	RGD:5509061	20260402	MGI			
1557146	Hoxc13	homeobox C13	gene	MP:0013436	increased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11159343
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689686
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160204	MGI			PMID:23633960
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557147	H1f3	H1.3 linker histone, cluster member	gene	MP:0012156	rostral-caudal axis duplication		IAGP		N	RGD:5509061	20141003	MGI			PMID:12808097
1557148	Vnn3	vanin 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20240523	MGI			
1557148	Vnn3	vanin 3	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20230601	MGI			
1557148	Vnn3	vanin 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1557150	Golga4	golgin A4	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20231207	MGI			
1557150	Golga4	golgin A4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22114267
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:22114267
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22114267
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899651
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21317887
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10811224
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557151	Map2k7	mitogen-activated protein kinase kinase 7	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:21317887
1557152	Edn3	endothelin 3	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001160
1557152	Edn3	endothelin 3	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5917257
1557152	Edn3	endothelin 3	gene	MP:0001048	absent enteric neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001160
1557152	Edn3	endothelin 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001160
1557152	Edn3	endothelin 3	gene	MP:0002557	abnormal social/conspecific interaction behavior		IEA		N	RGD:5509061	20111116	MGI			
1557152	Edn3	endothelin 3	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:14138974
1557152	Edn3	endothelin 3	gene	MP:0002731	megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:5917257
1557152	Edn3	endothelin 3	gene	MP:0002926	aganglionic megacolon		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001160
1557152	Edn3	endothelin 3	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:14138974
1557152	Edn3	endothelin 3	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:17516928
1557152	Edn3	endothelin 3	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:5917257
1557152	Edn3	endothelin 3	gene	MP:0002940	variable body spotting		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001160
1557152	Edn3	endothelin 3	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14138974
1557152	Edn3	endothelin 3	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14138974
1557152	Edn3	endothelin 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14138974
1557152	Edn3	endothelin 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5917257
1557152	Edn3	endothelin 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17516928
1557152	Edn3	endothelin 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8001160
1557153	Serac1	serine active site containing 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20190502	MGI			
1557153	Serac1	serine active site containing 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20190502	MGI			
1557153	Serac1	serine active site containing 1	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20181227	MGI			
1557153	Serac1	serine active site containing 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1557153	Serac1	serine active site containing 1	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20181227	MGI			
1557153	Serac1	serine active site containing 1	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0006037	abnormal mitochondrial fission		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0009453	enhanced contextual conditioning behavior		IEA		N	RGD:5509061	20211021	MGI			
1557153	Serac1	serine active site containing 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0010028	aciduria		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0010400	increased liver glycogen level		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0013806	encephalopathy		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0014388	decreased hepatocyte mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0014389	decreased skeletal muscle fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20201231	MGI			
1557153	Serac1	serine active site containing 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1557153	Serac1	serine active site containing 1	gene	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557153	Serac1	serine active site containing 1	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20220811	MGI			PMID:35235340
1557156	Tssk4	testis-specific serine kinase 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20180809	MGI			PMID:25361759
1557156	Tssk4	testis-specific serine kinase 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20180809	MGI			PMID:25361759
1557156	Tssk4	testis-specific serine kinase 4	gene	MP:0004222	iris synechia		IEA		N	RGD:5509061	20190502	MGI			
1557156	Tssk4	testis-specific serine kinase 4	gene	MP:0009280	decreased activated sperm motility		IAGP		N	RGD:5509061	20180809	MGI			PMID:25361759
1557156	Tssk4	testis-specific serine kinase 4	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25361759
1557156	Tssk4	testis-specific serine kinase 4	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25361759
1557156	Tssk4	testis-specific serine kinase 4	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20180809	MGI			PMID:25361759
1557157	Zfp704	zinc finger protein 704	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17693064
1557157	Zfp704	zinc finger protein 704	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0008058	abnormal DNA repair		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0009591	increased liver adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0010288	increased gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20240523	MGI			
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0014128	increased Harderian gland adenocarcinoma incidence		IAGP		N	RGD:5509061	20160317	MGI			PMID:21901109
1557158	Atad5	ATPase family, AAA domain containing 5	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:21901109
1557159	C1ra	complement component 1, r subcomponent A	gene	MP:0002282	abnormal trachea morphology		IEA		N	RGD:5509061	20170105	MGI			
1557159	C1ra	complement component 1, r subcomponent A	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20250508	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20241121	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767295
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20190207	MGI			PMID:30592498
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767295
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767295
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20190207	MGI			PMID:30592498
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767295
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20190207	MGI			PMID:30592498
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767295
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19767295
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0010895	increased lung compliance		IEA		N	RGD:5509061	20250508	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0011045	decreased lung elastance		IEA		N	RGD:5509061	20250508	MGI			
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0014333	short retina cone cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:19767295
1557161	Cngb3	cyclic nucleotide gated channel beta 3	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:19767295
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641550
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21986498
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:21986498
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641550
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641550
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641550
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0010957	abnormal aerobic respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23290137
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21641550
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21986498
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21986498
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557162	Ptpmt1	protein tyrosine phosphatase, mitochondrial 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:21986498
1557163	Mafa	MAF bZIP transcription factor A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923615
1557163	Mafa	MAF bZIP transcription factor A	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923615
1557163	Mafa	MAF bZIP transcription factor A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20213756
1557163	Mafa	MAF bZIP transcription factor A	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923615
1557163	Mafa	MAF bZIP transcription factor A	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923615
1557163	Mafa	MAF bZIP transcription factor A	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923615
1557163	Mafa	MAF bZIP transcription factor A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923615
1557163	Mafa	MAF bZIP transcription factor A	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15923615
1557168	Bsx	brain specific homeobox	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485440
1557168	Bsx	brain specific homeobox	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485440
1557168	Bsx	brain specific homeobox	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485440
1557168	Bsx	brain specific homeobox	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485440
1557168	Bsx	brain specific homeobox	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485440
1557168	Bsx	brain specific homeobox	gene	MP:0010249	lactation failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17485440
1557168	Bsx	brain specific homeobox	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17550780
1557168	Bsx	brain specific homeobox	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20160317	MGI			PMID:17485440
1557169	Lypd1	Ly6/Plaur domain containing 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19246390
1557169	Lypd1	Ly6/Plaur domain containing 1	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19246390
1557169	Lypd1	Ly6/Plaur domain containing 1	gene	MP:0002799	abnormal passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19246390
1557169	Lypd1	Ly6/Plaur domain containing 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19246390
1557169	Lypd1	Ly6/Plaur domain containing 1	gene	MP:0003459	increased fear-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19246390
1557171	Zfp553	zinc finger protein 553	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983912
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326152
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326152
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983912
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983912
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0005201	abnormal retina pigment epithelium morphology		IEA		N	RGD:5509061	20111116	MGI			
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0005240	abnormal amacrine cell morphology		IEA		N	RGD:5509061	20111116	MGI			
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983912
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326152
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326152
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16088326
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18245825
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983912
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008512	disorganized retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983912
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008512	disorganized retina inner nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008512	disorganized retina inner nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983912
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008516	disorganized retina outer nuclear layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008520	disorganized retina outer plexiform layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008520	disorganized retina outer plexiform layer		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008581	disorganized photoreceptor inner segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11983912
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:17652759
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200507	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0014333	short retina cone cell outer segment		IAGP		N	RGD:5509061	20240118	MGI			PMID:31174210
1557176	Rs1	retinoschisis (X-linked, juvenile) 1 (human)	gene	MP:0020816	decreased photoreceptor outer segment number		IAGP		N	RGD:5509061	20200116	MGI			PMID:29379415
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20111116	MGI			
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20150827	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0001529	abnormal vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0005534	decreased body temperature		IEA		N	RGD:5509061	20211021	MGI			
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0013140	excessive vocalization		IAGP		N	RGD:5509061	20141003	MGI			PMID:23936366
1557177	Ckap5	cytoskeleton associated protein 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557178	Znrf4	zinc and ring finger 4	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20260305	MGI			PMID:38084666
1557178	Znrf4	zinc and ring finger 4	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20260305	MGI			PMID:38084666
1557180	Lvrn	laeverin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:30745494
1557184	Lyzl1	lysozyme-like 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1557184	Lyzl1	lysozyme-like 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20170406	MGI			
1557189	Tspan6	tetraspanin 6	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20210401	MGI			PMID:28207852
1557189	Tspan6	tetraspanin 6	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20210401	MGI			PMID:28207852
1557189	Tspan6	tetraspanin 6	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20210401	MGI			PMID:28207852
1557189	Tspan6	tetraspanin 6	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20210401	MGI			PMID:28207852
1557190	Siglecl2	Siglec family like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557191	Lamtor2	late endosomal/lysosomal adaptor, MAPK and MTOR activator 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17178906
1557192	Pcdh10	protocadherin 10	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17721516
1557192	Pcdh10	protocadherin 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17721516
1557192	Pcdh10	protocadherin 10	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20221103	MGI			
1557192	Pcdh10	protocadherin 10	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20221103	MGI			
1557192	Pcdh10	protocadherin 10	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17721516
1557192	Pcdh10	protocadherin 10	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20221103	MGI			
1557192	Pcdh10	protocadherin 10	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17721516
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164512
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11118202
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16777961
1557193	Xrcc2	X-ray repair complementing defective repair in Chinese hamster cells 2	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:11118202
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200416	MGI			PMID:31730647
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20181011	MGI			
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20200416	MGI			PMID:31730647
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0004677	truncated ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11818962
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0004755	abnormal loop of Henle morphology		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141030	MGI			PMID:24700869
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0012547	spina bifida cystica		IAGP		N	RGD:5509061	20200402	MGI			PMID:31730647
1557198	Ttc21b	tetratricopeptide repeat domain 21B	gene	MP:0020383	decreased kidney epithelial cell primary cilium length		IAGP		N	RGD:5509061	20161013	MGI			PMID:24700869
1557199	Nyx	nyctalopin	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20141003	MGI			PMID:12506099
1557199	Nyx	nyctalopin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16597347
1557199	Nyx	nyctalopin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22896717
1557199	Nyx	nyctalopin	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9804152
1557199	Nyx	nyctalopin	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16597347
1557199	Nyx	nyctalopin	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9804152
1557199	Nyx	nyctalopin	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9804152
1557199	Nyx	nyctalopin	gene	MP:0010749	absent visual evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:9804152
1557203	Snrnp200	small nuclear ribonucleoprotein 200 (U5)	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20160811	MGI			
1557203	Snrnp200	small nuclear ribonucleoprotein 200 (U5)	gene	MP:0002750	exophthalmos		IEA		N	RGD:5509061	20230601	MGI			
1557203	Snrnp200	small nuclear ribonucleoprotein 200 (U5)	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20230601	MGI			
1557203	Snrnp200	small nuclear ribonucleoprotein 200 (U5)	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1557203	Snrnp200	small nuclear ribonucleoprotein 200 (U5)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557203	Snrnp200	small nuclear ribonucleoprotein 200 (U5)	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557205	Atg9a	autophagy related 9A	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20200310	MGI			PMID:19926846
1557205	Atg9a	autophagy related 9A	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19926846
1557205	Atg9a	autophagy related 9A	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:19926846
1557205	Atg9a	autophagy related 9A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:19926846
1557205	Atg9a	autophagy related 9A	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19926846
1557205	Atg9a	autophagy related 9A	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:19926846
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210520	MGI			
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210520	MGI			
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20231123	MGI			PMID:35840571
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20231123	MGI			PMID:35840571
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20231123	MGI			PMID:35840571
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20200402	MGI			
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0003063	increased coping response		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0003877	abnormal serotonergic neuron morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20231123	MGI			PMID:35840571
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20210520	MGI			
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0004844	abnormal vestibuloocular reflex		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210520	MGI			
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20241121	MGI			
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0005322	abnormal serotonin level		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20231123	MGI			PMID:35840571
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20231123	MGI			PMID:35840571
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20231123	MGI			PMID:35840571
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20231123	MGI			PMID:35840571
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0020379	abnormal sucrose solution preference		IAGP		N	RGD:5509061	20220811	MGI			PMID:35789858
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20231123	MGI			PMID:35840571
1557207	Slitrk2	SLIT and NTRK-like family, member 2	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1557208	Cd177	CD177 antigen	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20160324	MGI			PMID:25359465
1557208	Cd177	CD177 antigen	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20160324	MGI			PMID:25359465
1557208	Cd177	CD177 antigen	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20160324	MGI			PMID:25359465
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20170105	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20200402	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20181227	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160114	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20160114	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0003443	increased circulating glycerol level		IEA		N	RGD:5509061	20211021	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20170105	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200402	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20170105	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0005014	increased B cell number		IEA		N	RGD:5509061	20160804	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20160114	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160114	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160114	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20181227	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0008040	decreased NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0008210	increased mature B cell number		IEA		N	RGD:5509061	20160804	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0008347	decreased gamma-delta T cell number		IEA		N	RGD:5509061	20160804	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20160114	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200402	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20181227	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0010182	decreased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0010851	decreased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20201231	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20190711	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0012767	increased KLRG1-positive NK cell number		IEA		N	RGD:5509061	20160804	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0013022	increased Ly6C high monocyte number		IEA		N	RGD:5509061	20160804	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0013025	increased Ly6C low monocyte number		IEA		N	RGD:5509061	20160804	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0013513	decreased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0013519	decreased CD4-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0013522	decreased memory-marker CD4-positive NK T cell number		IEA		N	RGD:5509061	20201231	MGI			
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:23851121
1557209	Clpp	caseinolytic mitochondrial matrix peptidase proteolytic subunit	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20190711	MGI			PMID:23851121
1557210	Fn3k	fructosamine 3 kinase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16819943
1557210	Fn3k	fructosamine 3 kinase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16819943
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20250508	MGI			
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0003324	increased liver adenoma incidence		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20250508	MGI			
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0005284	increased saturated fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20250508	MGI			
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0005342	abnormal intestinal lipid absorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0006084	abnormal circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0010140	phlebitis		IAGP		N	RGD:5509061	20201224	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0014010	abnormal peroxisome morphology		IAGP		N	RGD:5509061	20200227	MGI			PMID:31207289
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:24503136
1557211	Pex1	peroxisomal biogenesis factor 1	gene	MP:0031158	abnormal venous thrombosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:31207289
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725384
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21546531
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:27162334
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725384
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691151
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:11853768
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725384
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691151
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20150129	MGI			PMID:22807293
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007830
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:11853768
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:27162334
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007830
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0003730	abnormal photoreceptor inner segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007830
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21546531
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007830
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20150129	MGI			PMID:22807293
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007830
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20150129	MGI			PMID:22807293
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0004175	telangiectasia		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725384
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14691151
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007830
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12651948
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007830
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725384
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12651948
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21546531
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008451	retina rod cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12651948
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725384
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725384
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20007830
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20150129	MGI			PMID:22807293
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20170126	MGI			PMID:11853768
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21546531
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21546531
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10725384
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:21546531
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557212	Rpgr	retinitis pigmentosa GTPase regulator	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20170126	MGI			PMID:22563472
1557213	Dtx3l	deltex 3-like, E3 ubiquitin ligase	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1557213	Dtx3l	deltex 3-like, E3 ubiquitin ligase	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220519	MGI			
1557213	Dtx3l	deltex 3-like, E3 ubiquitin ligase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1557213	Dtx3l	deltex 3-like, E3 ubiquitin ligase	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210826	MGI			
1557213	Dtx3l	deltex 3-like, E3 ubiquitin ligase	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20200402	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201231	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20181227	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20250508	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20250508	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1557214	Trim39	tripartite motif-containing 39	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20181227	MGI			
1557215	Hoxd3	homeobox D3	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557215	Hoxd3	homeobox D3	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1557215	Hoxd3	homeobox D3	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557215	Hoxd3	homeobox D3	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1557215	Hoxd3	homeobox D3	gene	MP:0001051	abnormal somatic motor system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12954718
1557215	Hoxd3	homeobox D3	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7910549
1557215	Hoxd3	homeobox D3	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557215	Hoxd3	homeobox D3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557215	Hoxd3	homeobox D3	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1557215	Hoxd3	homeobox D3	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1557215	Hoxd3	homeobox D3	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7910549
1557215	Hoxd3	homeobox D3	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1557215	Hoxd3	homeobox D3	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557215	Hoxd3	homeobox D3	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557215	Hoxd3	homeobox D3	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557215	Hoxd3	homeobox D3	gene	MP:0003955	abnormal ultimobranchial body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1557215	Hoxd3	homeobox D3	gene	MP:0004568	fusion of glossopharyngeal and vagus nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557215	Hoxd3	homeobox D3	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557215	Hoxd3	homeobox D3	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7910549
1557215	Hoxd3	homeobox D3	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1557215	Hoxd3	homeobox D3	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7910549
1557215	Hoxd3	homeobox D3	gene	MP:0004659	abnormal odontoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557215	Hoxd3	homeobox D3	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12954718
1557215	Hoxd3	homeobox D3	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:7910549
1557215	Hoxd3	homeobox D3	gene	MP:0009879	abnormal arcus anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557215	Hoxd3	homeobox D3	gene	MP:0009899	hyoid bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1557215	Hoxd3	homeobox D3	gene	MP:0010701	fusion of atlas and odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557215	Hoxd3	homeobox D3	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:7910549
1557215	Hoxd3	homeobox D3	gene	MP:0010729	absent arcus anterior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557215	Hoxd3	homeobox D3	gene	MP:0010730	absent odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557215	Hoxd3	homeobox D3	gene	MP:0010730	absent odontoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:7910549
1557215	Hoxd3	homeobox D3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557215	Hoxd3	homeobox D3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7910549
1557215	Hoxd3	homeobox D3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557215	Hoxd3	homeobox D3	gene	MP:0011513	abnormal vertebral artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7910549
1557215	Hoxd3	homeobox D3	gene	MP:0011576	absent cervical atlas		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557215	Hoxd3	homeobox D3	gene	MP:0011576	absent cervical atlas		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1557215	Hoxd3	homeobox D3	gene	MP:0013290	persistent ultimobranchial bodies		IAGP		N	RGD:5509061	20150122	MGI			PMID:9520319
1557215	Hoxd3	homeobox D3	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20150305	MGI			PMID:9520319
1557215	Hoxd3	homeobox D3	gene	MP:0030871	abnormal inferior horn of thyroid cartilage morphology		IAGP		N	RGD:5509061	20181101	MGI			PMID:7913519
1557217	Gstm4	glutathione S-transferase, mu 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1557217	Gstm4	glutathione S-transferase, mu 4	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20191128	MGI			
1557218	Eda2r	ectodysplasin A2 receptor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749376
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938851
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20260625	MGI			PMID:37480470
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0003092	decreased cornea stroma thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938851
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938851
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:37480470
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0005301	abnormal cornea endothelium morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:37480470
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:16938851
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557219	Chst5	carbohydrate sulfotransferase 5	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20260625	MGI			PMID:37480470
1557220	Pml	promyelocytic leukemia	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488655
1557220	Pml	promyelocytic leukemia	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488655
1557220	Pml	promyelocytic leukemia	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364283
1557220	Pml	promyelocytic leukemia	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488655
1557220	Pml	promyelocytic leukemia	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488655
1557220	Pml	promyelocytic leukemia	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488655
1557220	Pml	promyelocytic leukemia	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364283
1557220	Pml	promyelocytic leukemia	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364283
1557220	Pml	promyelocytic leukemia	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488655
1557220	Pml	promyelocytic leukemia	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0004049	increased acute promyelocytic leukemia incidence		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364283
1557220	Pml	promyelocytic leukemia	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488655
1557220	Pml	promyelocytic leukemia	gene	MP:0008886	abnormal PML bodies		IAGP		N	RGD:5509061	20180830	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364283
1557220	Pml	promyelocytic leukemia	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364283
1557220	Pml	promyelocytic leukemia	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488655
1557220	Pml	promyelocytic leukemia	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9488655
1557220	Pml	promyelocytic leukemia	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557220	Pml	promyelocytic leukemia	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:29191918
1557220	Pml	promyelocytic leukemia	gene	MP:0031058	hepatosplenomegaly		IAGP		N	RGD:5509061	20230615	MGI			PMID:23656786
1557223	Atp11b	ATPase, class VI, type 11B	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210520	MGI			
1557223	Atp11b	ATPase, class VI, type 11B	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20220519	MGI			
1557223	Atp11b	ATPase, class VI, type 11B	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1557223	Atp11b	ATPase, class VI, type 11B	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20220519	MGI			
1557224	Atg3	autophagy related 3	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21421856
1557224	Atg3	autophagy related 3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20200310	MGI			PMID:21421856
1557224	Atg3	autophagy related 3	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:21421856
1557224	Atg3	autophagy related 3	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21421856
1557224	Atg3	autophagy related 3	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18768753
1557224	Atg3	autophagy related 3	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21421856
1557224	Atg3	autophagy related 3	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21421856
1557224	Atg3	autophagy related 3	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:27303042
1557224	Atg3	autophagy related 3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21421856
1557224	Atg3	autophagy related 3	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21421856
1557224	Atg3	autophagy related 3	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:18768753
1557224	Atg3	autophagy related 3	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:27303042
1557224	Atg3	autophagy related 3	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18768753
1557224	Atg3	autophagy related 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200310	MGI			PMID:18768753
1557224	Atg3	autophagy related 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18768753
1557224	Atg3	autophagy related 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557224	Atg3	autophagy related 3	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18768753
1557224	Atg3	autophagy related 3	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:21421856
1557225	Ddx19b	DEAD box helicase 19b	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1557225	Ddx19b	DEAD box helicase 19b	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20210506	MGI			PMID:30699353
1557225	Ddx19b	DEAD box helicase 19b	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20210506	MGI			PMID:30699353
1557225	Ddx19b	DEAD box helicase 19b	gene	MP:0008562	increased interferon-alpha secretion		IAGP		N	RGD:5509061	20210506	MGI			PMID:30699353
1557225	Ddx19b	DEAD box helicase 19b	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20210506	MGI			PMID:30699353
1557225	Ddx19b	DEAD box helicase 19b	gene	MP:0009198	abnormal male genitalia morphology		IEA		N	RGD:5509061	20230720	MGI			
1557225	Ddx19b	DEAD box helicase 19b	gene	MP:0010768	mortality/aging		IAGP		N	RGD:5509061	20210506	MGI			PMID:30699353
1557225	Ddx19b	DEAD box helicase 19b	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210506	MGI			PMID:30699353
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633973
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633973
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633973
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633973
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0003884	decreased macrophage cell number		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633973
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0011190	thick embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:14633973
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0014395	increased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0020423	abnormal mitochondrial biogenesis		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0021161	increased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0021162	increased heart left ventricle anterior wall thickness		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0031131	myocardial fiber disarray		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557226	Ecsit	ECSIT signalling integrator	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20260813	MGI			PMID:37395010
1557227	Heatr5b	HEAT repeat containing 5B	gene	MP:0014257	embryonic lethality prior to tooth bud stage, complete penetrance		IAGP		N	RGD:5509061	20231102	MGI			PMID:33824466
1557228	Col20a1	collagen, type XX, alpha 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1557230	Mospd1	motile sperm domain containing 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1557231	Styk1	serine/threonine/tyrosine kinase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:30758858
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20170504	MGI			
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20170504	MGI			
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20211021	MGI			
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20220811	MGI			PMID:35358843
1557234	Slc8b1	solute carrier family 8 (sodium/lithium/calcium exchanger), member B1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:35358843
1557237	Neurl3	neuralized E3 ubiquitin protein ligase 3	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20240620	MGI			PMID:35792897
1557237	Neurl3	neuralized E3 ubiquitin protein ligase 3	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20240620	MGI			PMID:35792897
1557237	Neurl3	neuralized E3 ubiquitin protein ligase 3	gene	MP:0031024	increased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240620	MGI			PMID:35792897
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20141003	MGI			
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20141003	MGI			
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20160804	MGI			
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0003345	decreased rib number		IEA		N	RGD:5509061	20141003	MGI			
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0004648	decreased thoracic vertebrae number		IEA		N	RGD:5509061	20141003	MGI			
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:22696294
1557238	Zc3hc1	zinc finger, C3HC type 1	gene	MP:0031474	increased female germ cell apoptosis		IAGP		N	RGD:5509061	20230615	MGI			PMID:22696294
1557239	Crabp1	cellular retinoic acid binding protein I	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1557239	Crabp1	cellular retinoic acid binding protein I	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7768191
1557239	Crabp1	cellular retinoic acid binding protein I	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20181227	MGI			
1557239	Crabp1	cellular retinoic acid binding protein I	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210128	MGI			
1557239	Crabp1	cellular retinoic acid binding protein I	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7768191
1557239	Crabp1	cellular retinoic acid binding protein I	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:7890139
1557239	Crabp1	cellular retinoic acid binding protein I	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:8090764
1557239	Crabp1	cellular retinoic acid binding protein I	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20181227	MGI			
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20111116	MGI			
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0000538	abnormal urinary bladder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001685	abnormal endoderm development		IEA		N	RGD:5509061	20111116	MGI			
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001695	abnormal gastrulation		IEA		N	RGD:5509061	20111116	MGI			
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20111116	MGI			
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002084	abnormal developmental patterning		IEA		N	RGD:5509061	20111116	MGI			
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20111116	MGI			
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002660	abnormal caput epididymis morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:22187431
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22213803
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0013601	increased testis apoptosis		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20220630	MGI			PMID:29259204
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0020599	increased cerebral cortex cell density		IAGP		N	RGD:5509061	20260716	MGI			PMID:19686682
1557240	Huwe1	HECT, UBA and WWE domain containing 1	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:22213803
1557241	Tmem120a	transmembrane protein 120A	gene	MP:0020374	abnormal nocifensive behavior		IAGP		N	RGD:5509061	20210204	MGI			PMID:32084332
1557241	Tmem120a	transmembrane protein 120A	gene	MP:0020955	increased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20210204	MGI			PMID:32084332
1557242	Zfp706	zinc finger protein 706	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1557242	Zfp706	zinc finger protein 706	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1557242	Zfp706	zinc finger protein 706	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1557242	Zfp706	zinc finger protein 706	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557243	Gpd1l	glycerol-3-phosphate dehydrogenase 1-like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1557244	Trim66	tripartite motif-containing 66	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1557244	Trim66	tripartite motif-containing 66	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20160804	MGI			
1557244	Trim66	tripartite motif-containing 66	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20240627	MGI			PMID:38719749
1557244	Trim66	tripartite motif-containing 66	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1557244	Trim66	tripartite motif-containing 66	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1557244	Trim66	tripartite motif-containing 66	gene	MP:0010723	paternal effect		IAGP		N	RGD:5509061	20240627	MGI			PMID:38719749
1557244	Trim66	tripartite motif-containing 66	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:38719749
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804213
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314171
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000794	abnormal parietal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22810622
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804213
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000861	disorganized barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16862160
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885734
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885734
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22153375
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12853418
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804213
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16251442
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:21885734
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0002578	impaired ability to fire action potentials		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804213
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:16908411
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219273
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0002917	decreased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:19607846
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804213
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804213
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21050275
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804213
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219273
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0008285	abnormal hippocampus granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804213
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0008431	abnormal short-term spatial reference memory		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0008443	absent subplate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20159449
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21050275
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23785142
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219273
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0010011	ectopic hippocampus pyramidal cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22219273
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0010011	ectopic hippocampus pyramidal cells		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20141003	MGI			PMID:19607846
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0010770	preweaning lethality		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522044
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10804213
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314171
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0011150	abnormal hippocampus stratum oriens morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0014375	increased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0014382	increased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0015050	abnormal presynapse morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:22219273
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0015055	decreased synapse density		IAGP		N	RGD:5509061	20260813	MGI			PMID:22219273
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20200827	MGI			PMID:31780330
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0020594	decreased cerebral cortex cell number		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0021112	impaired social recognition		IAGP		N	RGD:5509061	20241128	MGI			PMID:36924980
1557246	Neurod6	neurogenic differentiation 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:22153375
1557247	Tut1	terminal uridylyl transferase 1, U6 snRNA-specific	gene	MP:0031661	prenatal lethality prior to heart atrial septation, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1557248	Aoah	acyloxyacyl hydrolase	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810692
1557249	Slc35f1	solute carrier family 35, member F1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1557249	Slc35f1	solute carrier family 35, member F1	gene	MP:0005571	decreased lactate dehydrogenase level		IEA		N	RGD:5509061	20160804	MGI			
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33340069
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20210617	MGI			PMID:33340069
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20210617	MGI			PMID:33340069
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33340069
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33340069
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20210617	MGI			PMID:33340069
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20210617	MGI			PMID:33340069
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0020358	abnormal inhibitory synapse morphology		IAGP		N	RGD:5509061	20210617	MGI			PMID:33340069
1557252	Ncoa7	nuclear receptor coactivator 7	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20210617	MGI			PMID:33340069
1557254	Gpr160	G protein-coupled receptor 160	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1557254	Gpr160	G protein-coupled receptor 160	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1557254	Gpr160	G protein-coupled receptor 160	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1557256	Hcfc1	host cell factor C1	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20220721	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20220721	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0006411	upturned snout		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0010499	abnormal ventricle myocardium morphology		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220721	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220217	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0011277	decreased tail pigmentation		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0012085	midface hypoplasia		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0012335	increased circulating homocysteine level		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20170615	MGI			PMID:26921005
1557256	Hcfc1	host cell factor C1	gene	MP:0030066	short face		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0030630	increased circulating methylmalonic acid level		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557256	Hcfc1	host cell factor C1	gene	MP:0030930	decreased digit pigmentation		IAGP		N	RGD:5509061	20220210	MGI			PMID:35013307
1557257	Sspo	SCO-spondin	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20210826	MGI			
1557257	Sspo	SCO-spondin	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1557257	Sspo	SCO-spondin	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210826	MGI			
1557257	Sspo	SCO-spondin	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20240307	MGI			PMID:38049798
1557257	Sspo	SCO-spondin	gene	MP:0013908	small lateral ventricles		IAGP		N	RGD:5509061	20240307	MGI			PMID:38049798
1557257	Sspo	SCO-spondin	gene	MP:0013909	small third ventricle		IAGP		N	RGD:5509061	20240307	MGI			PMID:38049798
1557257	Sspo	SCO-spondin	gene	MP:0014402	abnormal Reissner's fiber morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:38049798
1557259	Klhl4	kelch-like 4	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20190725	MGI			
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0009710	anhedonia		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0012293	impaired active avoidance behavior		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0014413	decreased depression-related behavior		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0020870	decreased thigmotaxis		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557260	Rasgef1b	RasGEF domain family, member 1B	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20250724	MGI			PMID:38048936
1557261	Akr1c19	aldo-keto reductase family 1, member C19	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240222	MGI			PMID:34843575
1557261	Akr1c19	aldo-keto reductase family 1, member C19	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1557261	Akr1c19	aldo-keto reductase family 1, member C19	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1557262	Garnl3	GTPase activating RANGAP domain-like 3	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1557264	Sergef	secretion regulating guanine nucleotide exchange factor	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20260402	MGI			
1557264	Sergef	secretion regulating guanine nucleotide exchange factor	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1557264	Sergef	secretion regulating guanine nucleotide exchange factor	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210128	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20241226	MGI			PMID:39269275
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20241226	MGI			PMID:39269275
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20241226	MGI			PMID:39269275
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20241226	MGI			PMID:39269275
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20241226	MGI			PMID:39269275
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20241226	MGI			PMID:39269275
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0020362	abnormal male germ cell physiology		IAGP		N	RGD:5509061	20241226	MGI			PMID:39269275
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20241226	MGI			PMID:39269275
1557266	Tmc7	transmembrane channel-like gene family 7	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20241226	MGI			PMID:39269275
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326356
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326356
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326356
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326356
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20160811	MGI			
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326356
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326356
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326356
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:15326356
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15326356
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1557267	Nobox	NOBOX oogenesis homeobox	gene	MP:0031382	absent secondary ovarian follicles		IAGP		N	RGD:5509061	20220407	MGI			PMID:15326356
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20230601	MGI			
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20200514	MGI			
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0003394	increased cardiac output		IEA		N	RGD:5509061	20230601	MGI			
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20240523	MGI			
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20211021	MGI			
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0011951	increased cardiac stroke volume		IEA		N	RGD:5509061	20230601	MGI			
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1557268	Psd3	pleckstrin and Sec7 domain containing 3	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230601	MGI			
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0009093	oocyte degeneration		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24155305
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0031018	decreased granulosa cell proliferation		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0031020	premature ovarian failure		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0031239	increased atretic ovarian follicle number		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220505	MGI			PMID:34930897
1557269	Cpeb3	cytoplasmic polyadenylation element binding protein 3	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220630	MGI			PMID:34930897
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151231	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0003213	decreased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0003458	decreased circulating ketone body level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230601	MGI			
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005335	abnormal gonadal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20210128	MGI			
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0009117	abnormal white fat cell morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0009299	decreased mesenteric fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654663
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0011019	abnormal adaptive thermogenesis		IAGP		N	RGD:5509061	20160128	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:18682832
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0030016	increased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:25477509
1557270	Cidec	cell death-inducing DFFA-like effector c	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:18654663
1557271	Dtx3	deltex 3, E3 ubiquitin ligase	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20260402	MGI			
1557271	Dtx3	deltex 3, E3 ubiquitin ligase	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1557272	Tfdp1	transcription factor Dp 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
1557272	Tfdp1	transcription factor Dp 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
1557272	Tfdp1	transcription factor Dp 1	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
1557272	Tfdp1	transcription factor Dp 1	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
1557272	Tfdp1	transcription factor Dp 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
1557272	Tfdp1	transcription factor Dp 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
1557272	Tfdp1	transcription factor Dp 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
1557272	Tfdp1	transcription factor Dp 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
1557272	Tfdp1	transcription factor Dp 1	gene	MP:0012131	small visceral yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588846
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1018005
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000161	scoliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23303524
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23303524
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000441	increased cranium width		IAGP		N	RGD:5509061	20171123	MGI			PMID:1018005
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861288
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942421
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589192
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861288
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942421
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589192
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000866	cerebellum vermis hypoplasia		IAGP		N	RGD:5509061	20221117	MGI			PMID:15450095
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:1018005
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861288
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000919	cranioschisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1018005
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000919	cranioschisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861288
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:1018005
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861288
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20221117	MGI			PMID:15450095
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861288
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23303524
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23303524
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15384171
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23303524
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861288
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861288
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589192
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16589192
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23303524
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23303524
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942421
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003085	abnormal egg cylinder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23471918
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20160331	MGI			PMID:23471918
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23303524
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23303524
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23471918
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004559	small allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004713	split notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0005034	abnormal anus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0005224	abnormal left-right axis symmetry of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0005236	abnormal olfactory nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0008818	abnormal interfrontal bone morphology		IAGP		N	RGD:5509061	20171123	MGI			PMID:1018005
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0009916	absent hyoid bone greater horns		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0009959	abnormal cerebellar hemisphere morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:15450095
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0009990	abnormal cerebellum vermis lobule III morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:15450095
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0009993	abnormal cerebellum vermis lobule V morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:15450095
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010807	abnormal stomach position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010853	abnormal lung position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010854	lung situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0010854	lung situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011042	abnormal horizontal vestibuloocular reflex		IAGP		N	RGD:5509061	20221117	MGI			PMID:15450095
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10861288
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23184148
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011660	ectopia cordis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0011665	d-loop transposition of the great arteries		IAGP		N	RGD:5509061	20240118	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0012156	rostral-caudal axis duplication		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0012739	abnormal anterior primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397896
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0020530	disorganized thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:11959836
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0030100	hemifacial hypoplasia		IAGP		N	RGD:5509061	20170928	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0030285	mandibular coronoid process hypoplasia		IAGP		N	RGD:5509061	20171102	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0031345	developmental cataract		IAGP		N	RGD:5509061	20220217	MGI			PMID:17127413
1557273	Zic3	zinc finger protein of the cerebellum 3	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20221117	MGI			PMID:15450095
1557275	Lhpp	phospholysine phosphohistidine inorganic pyrophosphate phosphatase	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20251127	MGI			PMID:37573508
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0003894	abnormal Purkinje cell innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17030622
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1557277	Cbln3	cerebellin 3 precursor protein	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20211021	MGI			
1557278	Repin1	replication initiator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
1557278	Repin1	replication initiator 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
1557278	Repin1	replication initiator 1	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
1557278	Repin1	replication initiator 1	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
1557278	Repin1	replication initiator 1	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20170713	MGI			PMID:27402271
1557279	Pabpn1l	poly(A)binding protein nuclear 1-like	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:32558204
1557279	Pabpn1l	poly(A)binding protein nuclear 1-like	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20210429	MGI			PMID:32558204
1557279	Pabpn1l	poly(A)binding protein nuclear 1-like	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20210429	MGI			PMID:32558204
1557280	Supt5	suppressor of Ty 5, DSIF elongation factor subunit	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20160114	MGI			
1557280	Supt5	suppressor of Ty 5, DSIF elongation factor subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557280	Supt5	suppressor of Ty 5, DSIF elongation factor subunit	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20220224	MGI			PMID:29514850
1557282	Dmkn	dermokine	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20191010	MGI			PMID:24794495
1557282	Dmkn	dermokine	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20191010	MGI			PMID:24794495
1557282	Dmkn	dermokine	gene	MP:0009605	decreased keratohyalin granule number		IAGP		N	RGD:5509061	20191010	MGI			PMID:24794495
1557282	Dmkn	dermokine	gene	MP:0009607	decreased keratohyalin granule size		IAGP		N	RGD:5509061	20191010	MGI			PMID:24794495
1557283	Otud1	OTU domain containing 1	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20220901	MGI			PMID:32075857
1557283	Otud1	OTU domain containing 1	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20220901	MGI			PMID:32075857
1557283	Otud1	OTU domain containing 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20220901	MGI			PMID:32075857
1557283	Otud1	OTU domain containing 1	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20220901	MGI			PMID:32075857
1557283	Otud1	OTU domain containing 1	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20220901	MGI			PMID:32075857
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589882
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20181227	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0000783	abnormal forebrain morphology		IEA		N	RGD:5509061	20181227	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0000841	abnormal hindbrain morphology		IEA		N	RGD:5509061	20181227	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0000897	abnormal midbrain morphology		IEA		N	RGD:5509061	20181227	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15640247
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589882
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22045912
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:15640247
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589882
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22045912
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22045912
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20170105	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0004156	abnormal QT variability		IEA		N	RGD:5509061	20220519	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15640247
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1557284	Cecr2	CECR2, histone acetyl-lysine reader	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589882
1557286	Nags	N-acetylglutamate synthase	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503289
1557286	Nags	N-acetylglutamate synthase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503289
1557286	Nags	N-acetylglutamate synthase	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503289
1557286	Nags	N-acetylglutamate synthase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503289
1557286	Nags	N-acetylglutamate synthase	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503289
1557286	Nags	N-acetylglutamate synthase	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503289
1557286	Nags	N-acetylglutamate synthase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22503289
1557286	Nags	N-acetylglutamate synthase	gene	MP:0020837	decreased circulating citrulline level		IAGP		N	RGD:5509061	20180712	MGI			PMID:22503289
1557288	Cenpv	centromere protein V	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1557288	Cenpv	centromere protein V	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220106	MGI			PMID:34764261
1557288	Cenpv	centromere protein V	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20220106	MGI			PMID:34764261
1557288	Cenpv	centromere protein V	gene	MP:0009761	abnormal meiotic spindle morphology		IAGP		N	RGD:5509061	20220106	MGI			PMID:34764261
1557288	Cenpv	centromere protein V	gene	MP:0014443	impaired polar body extrusion		IAGP		N	RGD:5509061	20240509	MGI			PMID:34764261
1557290	Myo3a	myosin IIIA	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557290	Myo3a	myosin IIIA	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21165622
1557290	Myo3a	myosin IIIA	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21165622
1557290	Myo3a	myosin IIIA	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21165622
1557290	Myo3a	myosin IIIA	gene	MP:0004408	decreased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21165622
1557290	Myo3a	myosin IIIA	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1557290	Myo3a	myosin IIIA	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1557290	Myo3a	myosin IIIA	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21165622
1557290	Myo3a	myosin IIIA	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240321	MGI			PMID:26926603
1557290	Myo3a	myosin IIIA	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220519	MGI			
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20231207	MGI			
1557291	Spg11	SPG11, spatacsin vesicle trafficking associated	gene	MP:0012506	brain atrophy		IAGP		N	RGD:5509061	20160915	MGI			PMID:26284655
1557292	Zcchc13	zinc finger, CCHC domain containing 13	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004851
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004851
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004851
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004851
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20231207	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004851
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0003164	decreased posterior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0003442	decreased circulating glycerol level		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20250508	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004851
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0004425	abnormal otolith organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19004851
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20241121	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20250508	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0011238	abnormal inner ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24086156
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0011952	decreased cardiac stroke volume		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0011971	increased circulating lactate dehydrogenase level		IEA		N	RGD:5509061	20230601	MGI			
1557293	Lrig3	leucine-rich repeats and immunoglobulin-like domains 3	gene	MP:0020204	abnormal heart left ventricle weight		IAGP		N	RGD:5509061	20171116	MGI			PMID:27009049
1557295	2810408A11Rik	RIKEN cDNA 2810408A11 gene	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20141003	MGI			
1557295	2810408A11Rik	RIKEN cDNA 2810408A11 gene	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20141003	MGI			
1557295	2810408A11Rik	RIKEN cDNA 2810408A11 gene	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20160804	MGI			
1557295	2810408A11Rik	RIKEN cDNA 2810408A11 gene	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1557295	2810408A11Rik	RIKEN cDNA 2810408A11 gene	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160804	MGI			
1557295	2810408A11Rik	RIKEN cDNA 2810408A11 gene	gene	MP:0008044	increased NK cell number		IEA		N	RGD:5509061	20141003	MGI			
1557295	2810408A11Rik	RIKEN cDNA 2810408A11 gene	gene	MP:0008045	decreased NK cell number		IEA		N	RGD:5509061	20160804	MGI			
1557295	2810408A11Rik	RIKEN cDNA 2810408A11 gene	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20141003	MGI			
1557297	Rhox9	reproductive homeobox 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11689708
1557300	Actr3b	ARP3 actin-related protein 3B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20171207	MGI			PMID:26847029
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20111116	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20171207	MGI			PMID:26847029
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20111116	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0001689	incomplete somite formation		IEA		N	RGD:5509061	20111116	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0001695	abnormal gastrulation		IEA		N	RGD:5509061	20111116	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20111116	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0002084	abnormal developmental patterning		IEA		N	RGD:5509061	20111116	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20111116	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0003792	abnormal major salivary gland morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0004251	failure of heart looping		IEA		N	RGD:5509061	20111116	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0006208	lethality throughout fetal growth and development		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0008862	asymmetric snout		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20171207	MGI			PMID:26847029
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0009909	bifid tongue		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0013264	tongue ankylosis		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20221020	MGI			PMID:32692983
1557301	Bcor	BCL6 interacting corepressor	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:32692983
1557303	Supt7l	SPT7-like, STAGA complex gamma subunit	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1557303	Supt7l	SPT7-like, STAGA complex gamma subunit	gene	MP:0002074	abnormal hair texture		IEA		N	RGD:5509061	20160804	MGI			
1557303	Supt7l	SPT7-like, STAGA complex gamma subunit	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1557303	Supt7l	SPT7-like, STAGA complex gamma subunit	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160804	MGI			
1557305	Serpinb3a	serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3A	gene	MP:0002335	decreased airway responsiveness		IAGP		N	RGD:5509061	20141003	MGI			PMID:21126757
1557305	Serpinb3a	serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3A	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21126757
1557305	Serpinb3a	serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3A	gene	MP:0010862	decreased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21126757
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20211104	MGI			PMID:34424262
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20211104	MGI			PMID:34424262
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20211104	MGI			PMID:34424262
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0002271	abnormal pulmonary alveolar duct morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:34424262
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0003089	decreased skin tensile strength		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0003409	decreased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004126	thin hypodermis		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004348	long femur		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004370	long ulna		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0005099	abnormal ciliary body morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0009405	increased skeletal muscle fiber number		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0011157	abnormal hypodermis muscle layer morphology		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0011159	abnormal epidermal-dermal junction morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20211104	MGI			PMID:34424262
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20260430	MGI			PMID:41034152
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0014164	abnormal ciliary process morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0014176	abnormal cilary zonule morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:30060141
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0014176	abnormal cilary zonule morphology		IAGP		N	RGD:5509061	20211104	MGI			PMID:34424262
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0014176	abnormal cilary zonule morphology		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0014659	increased skin stiffness		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20211104	MGI			PMID:34424262
1557306	Adamts10	ADAM metallopeptidase with thrombospondin type 1 motif 10	gene	MP:0031212	decreased eye anterior chamber depth		IAGP		N	RGD:5509061	20260122	MGI			PMID:30201140
1557308	Dnajc27	DnaJ heat shock protein family (Hsp40) member C27	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20250508	MGI			
1557308	Dnajc27	DnaJ heat shock protein family (Hsp40) member C27	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20250508	MGI			
1557308	Dnajc27	DnaJ heat shock protein family (Hsp40) member C27	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20170314	MGI			PMID:24746703
1557308	Dnajc27	DnaJ heat shock protein family (Hsp40) member C27	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20170314	MGI			PMID:24746703
1557308	Dnajc27	DnaJ heat shock protein family (Hsp40) member C27	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20170314	MGI			PMID:24746703
1557308	Dnajc27	DnaJ heat shock protein family (Hsp40) member C27	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1557308	Dnajc27	DnaJ heat shock protein family (Hsp40) member C27	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20250508	MGI			
1557310	Bhlhe23	basic helix-loop-helix family, member e23	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363390
1557310	Bhlhe23	basic helix-loop-helix family, member e23	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363390
1557310	Bhlhe23	basic helix-loop-helix family, member e23	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:15363390
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0002273	abnormal pulmonary alveolus epithelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0002274	abnormal type I pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0004986	abnormal osteoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0008274	failure of bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0009908	protruding tongue		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0010449	heart right ventricle outflow tract stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0010827	small lung saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21214893
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19112494
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20089971
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0020138	delayed bone mineralization		IAGP		N	RGD:5509061	20180517	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0030949	abnormal Golgi vesicle transport		IAGP		N	RGD:5509061	20190725	MGI			PMID:29180569
1557313	Trip11	thyroid hormone receptor interactor 11	gene	MP:0030952	abnormal Golgi stack morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:29180569
1557314	Invs	inversin	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325766
1557314	Invs	inversin	gene	MP:0000542	left-sided isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325766
1557314	Invs	inversin	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230119	MGI			
1557314	Invs	inversin	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230119	MGI			
1557314	Invs	inversin	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744276
1557314	Invs	inversin	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325766
1557314	Invs	inversin	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0003197	nephrocalcinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12386294
1557314	Invs	inversin	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744276
1557314	Invs	inversin	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549278
1557314	Invs	inversin	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325766
1557314	Invs	inversin	gene	MP:0004159	double aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325766
1557314	Invs	inversin	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0004194	abnormal kidney pelvis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9744276
1557314	Invs	inversin	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0005083	abnormal biliary tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8480178
1557314	Invs	inversin	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0006062	abnormal vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0008461	left atrial isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0008933	abnormal motile primary cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549278
1557314	Invs	inversin	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0009145	abnormal pancreatic acinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0009149	decreased pancreatic acinar cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:9771707
1557314	Invs	inversin	gene	MP:0010431	atrial situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0010541	aorta hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325766
1557314	Invs	inversin	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325766
1557314	Invs	inversin	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0010854	lung situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16325766
1557314	Invs	inversin	gene	MP:0010854	lung situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1557314	Invs	inversin	gene	MP:0011250	abdominal situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9664638
1557314	Invs	inversin	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0011308	kidney corticomedullary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0011341	abnormal loop of Henle descending limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0011344	abnormal loop of Henle ascending limb thick segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0011352	proximal convoluted tubule brush border loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0011425	abnormal kidney interstitium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:15213262
1557314	Invs	inversin	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12386294
1557314	Invs	inversin	gene	MP:0012027	abnormal embryonic cilium location or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10549278
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210520	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20201022	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0003450	enlarged pancreas		IEA		N	RGD:5509061	20210128	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210520	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20241121	MGI			
1557315	Camk1d	calcium/calmodulin-dependent protein kinase ID	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698281
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698281
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698281
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698281
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698281
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0003085	abnormal egg cylinder morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698281
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0003895	increased ectoderm apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698281
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698281
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22698281
1557316	Vps41	VPS41 HOPS complex subunit	gene	MP:0030951	abnormal endocytosis		IAGP		N	RGD:5509061	20190725	MGI			PMID:22698281
1557317	Nwd2	NACHT and WD repeat domain containing 2	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20210128	MGI			
1557317	Nwd2	NACHT and WD repeat domain containing 2	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210128	MGI			
1557317	Nwd2	NACHT and WD repeat domain containing 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20200514	MGI			
1557317	Nwd2	NACHT and WD repeat domain containing 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20200514	MGI			
1557317	Nwd2	NACHT and WD repeat domain containing 2	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20200514	MGI			
1557317	Nwd2	NACHT and WD repeat domain containing 2	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20201022	MGI			
1557318	Zfyve19	zinc finger, FYVE domain containing 19	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1557318	Zfyve19	zinc finger, FYVE domain containing 19	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20221215	MGI			
1557318	Zfyve19	zinc finger, FYVE domain containing 19	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20220519	MGI			
1557318	Zfyve19	zinc finger, FYVE domain containing 19	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1557318	Zfyve19	zinc finger, FYVE domain containing 19	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220519	MGI			
1557319	Diaph2	diaphanous related formin 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20111116	MGI			
1557319	Diaph2	diaphanous related formin 2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1557319	Diaph2	diaphanous related formin 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1557319	Diaph2	diaphanous related formin 2	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1557319	Diaph2	diaphanous related formin 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20201022	MGI			
1557319	Diaph2	diaphanous related formin 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20111116	MGI			
1557319	Diaph2	diaphanous related formin 2	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20111116	MGI			
1557319	Diaph2	diaphanous related formin 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1557319	Diaph2	diaphanous related formin 2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1557319	Diaph2	diaphanous related formin 2	gene	MP:0005377	hearing/vestibular/ear phenotype		IAGP		N	RGD:5509061	20230420	MGI			PMID:36689403
1557319	Diaph2	diaphanous related formin 2	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1557319	Diaph2	diaphanous related formin 2	gene	MP:0009949	abnormal olfactory bulb granule cell layer morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:22246438
1557321	Golt1a	golgi transport 1A	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
1557321	Golt1a	golgi transport 1A	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1557321	Golt1a	golgi transport 1A	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1557321	Golt1a	golgi transport 1A	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210520	MGI			
1557321	Golt1a	golgi transport 1A	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
1557325	Ifne	interferon epsilon	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:23449591
1557325	Ifne	interferon epsilon	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23449591
1557325	Ifne	interferon epsilon	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23449591
1557325	Ifne	interferon epsilon	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23449591
1557326	Lypd6b	LY6/PLAUR domain containing 6B	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20221215	MGI			
1557326	Lypd6b	LY6/PLAUR domain containing 6B	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1557326	Lypd6b	LY6/PLAUR domain containing 6B	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210520	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20170105	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20170105	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20170105	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20210520	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20190919	MGI			PMID:31276534
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20170105	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20231207	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20170105	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20210826	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20211021	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0010580	decreased heart left ventricle size		IEA		N	RGD:5509061	20210520	MGI			
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:31276534
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:31276534
1557328	Eftud2	elongation factor Tu GTP binding domain containing 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557329	Aqp12	aquaporin 12	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1557329	Aqp12	aquaporin 12	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726746
1557329	Aqp12	aquaporin 12	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726746
1557329	Aqp12	aquaporin 12	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1557329	Aqp12	aquaporin 12	gene	MP:0009160	abnormal pancreatic acinar cell zymogen granule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726746
1557330	Dnah17	dynein, axonemal, heavy chain 17	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210506	MGI			PMID:31658987
1557330	Dnah17	dynein, axonemal, heavy chain 17	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1557330	Dnah17	dynein, axonemal, heavy chain 17	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20210506	MGI			PMID:31658987
1557330	Dnah17	dynein, axonemal, heavy chain 17	gene	MP:0002073	abnormal hair growth		IEA		N	RGD:5509061	20201022	MGI			
1557330	Dnah17	dynein, axonemal, heavy chain 17	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:31658987
1557330	Dnah17	dynein, axonemal, heavy chain 17	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:31658987
1557330	Dnah17	dynein, axonemal, heavy chain 17	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:31658987
1557330	Dnah17	dynein, axonemal, heavy chain 17	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31658987
1557331	Tdrd12	tudor domain containing 12	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897936
1557331	Tdrd12	tudor domain containing 12	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:24067652
1557331	Tdrd12	tudor domain containing 12	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897936
1557331	Tdrd12	tudor domain containing 12	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24067652
1557331	Tdrd12	tudor domain containing 12	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897936
1557331	Tdrd12	tudor domain containing 12	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24067652
1557331	Tdrd12	tudor domain containing 12	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24067652
1557331	Tdrd12	tudor domain containing 12	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24067652
1557331	Tdrd12	tudor domain containing 12	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24067652
1557331	Tdrd12	tudor domain containing 12	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897936
1557331	Tdrd12	tudor domain containing 12	gene	MP:0004929	decreased epididymis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897936
1557331	Tdrd12	tudor domain containing 12	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897936
1557331	Tdrd12	tudor domain containing 12	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24067652
1557331	Tdrd12	tudor domain containing 12	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19897936
1557331	Tdrd12	tudor domain containing 12	gene	MP:0008261	arrest of male meiosis		IEA		N	RGD:5509061	20141003	MGI			
1557331	Tdrd12	tudor domain containing 12	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:19897936
1557331	Tdrd12	tudor domain containing 12	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:24067652
1557332	Hmgb3	high mobility group box 3	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15358624
1557332	Hmgb3	high mobility group box 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714519
1557332	Hmgb3	high mobility group box 3	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:15358624
1557332	Hmgb3	high mobility group box 3	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:15358624
1557332	Hmgb3	high mobility group box 3	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15358624
1557332	Hmgb3	high mobility group box 3	gene	MP:0005460	abnormal leukopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15358624
1557332	Hmgb3	high mobility group box 3	gene	MP:0005564	increased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:15358624
1557332	Hmgb3	high mobility group box 3	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15358624
1557332	Hmgb3	high mobility group box 3	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15358624
1557332	Hmgb3	high mobility group box 3	gene	MP:0014992	enhanced erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:15358624
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19598121
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0011176	abnormal erythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0014078	small intestinal villus atrophy		IAGP		N	RGD:5509061	20160414	MGI			PMID:23505375
1557333	Tdp2	tyrosyl-DNA phosphodiesterase 2	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:23505375
1557334	Usp46	ubiquitin specific peptidase 46	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465912
1557334	Usp46	ubiquitin specific peptidase 46	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465912
1557334	Usp46	ubiquitin specific peptidase 46	gene	MP:0002863	improved righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465912
1557334	Usp46	ubiquitin specific peptidase 46	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19465912
1557334	Usp46	ubiquitin specific peptidase 46	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22720038
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210826	MGI			
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210826	MGI			
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210826	MGI			
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20160304	MGI			PMID:25517090
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20190502	MGI			
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20210826	MGI			
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210826	MGI			
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20210826	MGI			
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0008765	decreased mast cell degranulation		IAGP		N	RGD:5509061	20160304	MGI			PMID:25517090
1557337	Mrgprb2	MAS-related GPR, member B2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1557339	Ercc6l2	excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20211118	MGI			PMID:32355287
1557339	Ercc6l2	excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20211118	MGI			PMID:32355287
1557339	Ercc6l2	excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20211118	MGI			PMID:32355287
1557339	Ercc6l2	excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20211118	MGI			PMID:32355287
1557339	Ercc6l2	excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20211118	MGI			PMID:32355287
1557339	Ercc6l2	excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20211118	MGI			PMID:32355287
1557339	Ercc6l2	excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20211118	MGI			PMID:32355287
1557339	Ercc6l2	excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2	gene	MP:0008754	abnormal T cell receptor V(D)J recombination		IAGP		N	RGD:5509061	20211118	MGI			PMID:32355287
1557340	Arl6ip1	ADP-ribosylation factor-like 6 interacting protein 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1557340	Arl6ip1	ADP-ribosylation factor-like 6 interacting protein 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20170105	MGI			
1557340	Arl6ip1	ADP-ribosylation factor-like 6 interacting protein 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20170105	MGI			
1557340	Arl6ip1	ADP-ribosylation factor-like 6 interacting protein 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20170105	MGI			
1557340	Arl6ip1	ADP-ribosylation factor-like 6 interacting protein 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20170105	MGI			
1557342	Ccnb3	cyclin B3	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20190502	MGI			PMID:30723090
1557342	Ccnb3	cyclin B3	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20190502	MGI			PMID:30723090
1557342	Ccnb3	cyclin B3	gene	MP:0012736	abnormal polar body morphology		IAGP		N	RGD:5509061	20190502	MGI			PMID:30723090
1557343	Rnft1	ring finger protein, transmembrane 1	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20200514	MGI			
1557343	Rnft1	ring finger protein, transmembrane 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1557343	Rnft1	ring finger protein, transmembrane 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20250508	MGI			
1557344	Cnih3	cornichon family AMPA receptor auxiliary protein 3	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522044
1557344	Cnih3	cornichon family AMPA receptor auxiliary protein 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522044
1557344	Cnih3	cornichon family AMPA receptor auxiliary protein 3	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522044
1557344	Cnih3	cornichon family AMPA receptor auxiliary protein 3	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23522044
1557345	Tead1	TEA domain family member 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958896
1557345	Tead1	TEA domain family member 1	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958896
1557345	Tead1	TEA domain family member 1	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958896
1557345	Tead1	TEA domain family member 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958896
1557345	Tead1	TEA domain family member 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20160811	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958896
1557345	Tead1	TEA domain family member 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20181227	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141225	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20240523	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958896
1557345	Tead1	TEA domain family member 1	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958896
1557345	Tead1	TEA domain family member 1	gene	MP:0005543	decreased cornea thickness		IEA		N	RGD:5509061	20210128	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0008534	enlarged fourth ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958896
1557345	Tead1	TEA domain family member 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958896
1557345	Tead1	TEA domain family member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20210128	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0013217	abnormal posterior definitive endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18332127
1557345	Tead1	TEA domain family member 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557345	Tead1	TEA domain family member 1	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:18332127
1557346	Foxj2	forkhead box J2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210506	MGI			PMID:27316861
1557346	Foxj2	forkhead box J2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20210506	MGI			PMID:27316861
1557346	Foxj2	forkhead box J2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20210506	MGI			PMID:27316861
1557346	Foxj2	forkhead box J2	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20210506	MGI			PMID:27316861
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000233	abnormal blood flow velocity		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160707	MGI			PMID:10655541
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:19329542
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20160707	MGI			PMID:10655541
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20160707	MGI			PMID:15703193
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20160707	MGI			PMID:18178576
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000947	convulsive seizures		IEA		N	RGD:5509061	20151015	MGI			
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001007	abnormal sympathetic system morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20160707	MGI			PMID:18065780
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:15703193
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:18065780
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001220	epidermal necrosis		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160707	MGI			PMID:15703193
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210128	MGI			
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001378	abnormal ejaculation		IAGP		N	RGD:5509061	20230216	MGI			PMID:32865662
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160707	MGI			PMID:15703193
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20160707	MGI			PMID:10655541
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001443	poor grooming		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9920659
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20160707	MGI			PMID:15703193
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20160707	MGI			PMID:15703193
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20160707	MGI			PMID:15703193
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20230216	MGI			PMID:32865662
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20160707	MGI			PMID:10655541
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0001956	hypopnea		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:9920659
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160707	MGI			PMID:18178576
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20230216	MGI			PMID:32865662
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002738	hyperresponsive to tactile stimuli		IEA		N	RGD:5509061	20151015	MGI			
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:9920659
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18716219
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:18716219
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0002913	abnormal PNS synaptic transmission		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:19329542
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0003466	decreased single cell response threshold		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0003928	increased heart rate variability		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0004243	abnormal motor nerve collateral sprouting		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20160707	MGI			PMID:10655541
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:12515823
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0006404	abnormal lumbar dorsal root ganglion morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:18178576
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:18716219
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20160707	MGI			PMID:18178576
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20160707	MGI			PMID:18065780
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20160707	MGI			PMID:15703193
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18716219
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0009856	failure of ejaculation		IAGP		N	RGD:5509061	20230216	MGI			PMID:32865662
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0010506	prolonged RR interval		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20160707	MGI			PMID:23390132
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:10655541
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:15703193
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:18178576
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:19329542
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:20693262
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:20826664
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:22423102
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:10655541
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:20696672
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20180308	MGI			PMID:29371219
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0013178	tail necrosis		IAGP		N	RGD:5509061	20160707	MGI			PMID:18178576
1557347	Grm7	glutamate receptor, metabotropic 7	gene	MP:0031628	abnormal intromission		IAGP		N	RGD:5509061	20240704	MGI			PMID:32865662
1557349	Hmx3	H6 homeobox 3	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0000035	abnormal membranous labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0000037	abnormal lateral semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0000041	absent endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0001752	abnormal hypothalamus secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142028
1557349	Hmx3	H6 homeobox 3	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0002858	abnormal posterior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0003069	abnormal superior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0003161	absent lateral semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0003163	absent posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0003163	absent posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0003164	decreased posterior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0003166	decreased superior semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0004314	absent inner ear vestibule		IAGP		N	RGD:5509061	20141003	MGI			PMID:9389661
1557349	Hmx3	H6 homeobox 3	gene	MP:0004328	decreased vestibular hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0004329	vestibular saccular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0004331	vestibular saccular macula degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0004332	utricular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0004334	utricular macular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0004425	abnormal otolith organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0004427	abnormal vestibular labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0006011	abnormal endolymphatic duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557349	Hmx3	H6 homeobox 3	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1557349	Hmx3	H6 homeobox 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9435283
1557350	Pax9	paired box 9	gene	MP:0000090	absent premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0000094	absent alveolar process		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0000094	absent alveolar process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0000118	arrest of tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0000121	failure of tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0000128	growth retardation of molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1557350	Pax9	paired box 9	gene	MP:0000272	abnormal aorta morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1557350	Pax9	paired box 9	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0000430	absent maxillary shelf		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0000431	absent palatine bone horizontal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0000455	abnormal maxilla morphology		IEA		N	RGD:5509061	20260402	MGI			
1557350	Pax9	paired box 9	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1557350	Pax9	paired box 9	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1557350	Pax9	paired box 9	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0002256	abnormal laryngeal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0002650	abnormal ameloblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0003404	absent enamel		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20260402	MGI			
1557350	Pax9	paired box 9	gene	MP:0003931	absent molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0004537	abnormal palatine bone horizontal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0004552	fused tracheal cartilage rings		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0004791	absent lower incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0004914	absent ultimobranchial body		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0004915	abnormal Reichert's cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0004916	absent Reichert cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0005270	abnormal zygomatic bone morphology		IEA		N	RGD:5509061	20260402	MGI			
1557350	Pax9	paired box 9	gene	MP:0005382	craniofacial phenotype		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0006031	abnormal pharyngeal pouch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0006356	abnormal third pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0009843	decreased neural crest cell number		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0009885	abnormal palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0009913	abnormal hyoid bone greater horn morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0010355	abnormal first pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0010356	abnormal second pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0010465	aberrant origin of the right subclavian artery		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0011659	interrupted aortic arch, type b		IAGP		N	RGD:5509061	20231214	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0021207	abnormal autopod muscle morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0030084	tympanic ring hypoplasia		IAGP		N	RGD:5509061	20241031	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0030136	abnormal lower incisor morphology		IAGP		N	RGD:5509061	20171005	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0030335	absent third pharyngeal arch artery		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0030336	third pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0030340	absent fourth pharyngeal arch artery		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0030341	fourth pharyngeal arch artery hypoplasia		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0030459	abnormal tooth attrition		IAGP		N	RGD:5509061	20180125	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0030542	abnormal dentin development		IAGP		N	RGD:5509061	20180215	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0030608	decreased tooth number		IAGP		N	RGD:5509061	20180726	MGI			PMID:16236760
1557350	Pax9	paired box 9	gene	MP:0030608	decreased tooth number		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20180726	MGI			PMID:17610273
1557350	Pax9	paired box 9	gene	MP:0030610	absent teeth		IAGP		N	RGD:5509061	20180726	MGI			PMID:9732271
1557350	Pax9	paired box 9	gene	MP:0030870	abnormal superior horn of thyroid cartilage morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0030871	abnormal inferior horn of thyroid cartilage morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:34615475
1557350	Pax9	paired box 9	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:21420399
1557350	Pax9	paired box 9	gene	MP:0031460	abnormal palatal shelf morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:9732271
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001215	skin hypoplasia		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001247	dermal cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001725	abnormal umbilical cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002085	abnormal embryonic tissue morphology		IEA		N	RGD:5509061	20111116	MGI			
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002213	true hermaphroditism		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002759	abnormal caudal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0004323	sternum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0004360	absent ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0005543	decreased cornea thickness		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0006226	iris hypoplasia		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0009085	abnormal uterine horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0009264	failure of eyelid fusion		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760955
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0011156	abnormal hypodermis fat layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22412863
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0013283	failure of ventral body wall closure		IAGP		N	RGD:5509061	20191114	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0014280	forelimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:25451153
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:21768372
1557351	Porcn	porcupine O-acyltransferase	gene	MP:0031445	midline cleft upper lip		IAGP		N	RGD:5509061	20221103	MGI			PMID:25451153
1557352	Stk31	serine threonine kinase 31	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23929668
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24240089
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:24240089
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24240089
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557355	Idh2	isocitrate dehydrogenase 2 (NADP+), mitochondrial	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20220609	MGI			PMID:29527922
1557356	Rad51b	RAD51 paralog B	gene	MP:0006206	embryonic lethality between somite formation and embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10567591
1557356	Rad51b	RAD51 paralog B	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10567591
1557359	Brcc3	BRCA1/BRCA2-containing complex, subunit 3	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1557359	Brcc3	BRCA1/BRCA2-containing complex, subunit 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1557359	Brcc3	BRCA1/BRCA2-containing complex, subunit 3	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20211021	MGI			
1557359	Brcc3	BRCA1/BRCA2-containing complex, subunit 3	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1557359	Brcc3	BRCA1/BRCA2-containing complex, subunit 3	gene	MP:0008656	abnormal interleukin-1 beta secretion		IAGP		N	RGD:5509061	20251120	MGI			PMID:33107021
1557359	Brcc3	BRCA1/BRCA2-containing complex, subunit 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1557359	Brcc3	BRCA1/BRCA2-containing complex, subunit 3	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20251120	MGI			PMID:30787184
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20241121	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230119	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20170831	MGI			PMID:27329800
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0003562	abnormal pancreatic beta cell physiology		IAGP		N	RGD:5509061	20170831	MGI			PMID:27329800
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20230119	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20170831	MGI			PMID:27329800
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20210128	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20230119	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20170105	MGI			
1557361	Vps13c	vacuolar protein sorting 13C	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230119	MGI			
1557362	Zfp445	zinc finger protein 445	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210826	MGI			
1557362	Zfp445	zinc finger protein 445	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20181227	MGI			
1557362	Zfp445	zinc finger protein 445	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1557362	Zfp445	zinc finger protein 445	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1557362	Zfp445	zinc finger protein 445	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1557362	Zfp445	zinc finger protein 445	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557362	Zfp445	zinc finger protein 445	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1557363	Msh3	mutS homolog 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201022	MGI			
1557363	Msh3	mutS homolog 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1557363	Msh3	mutS homolog 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1557363	Msh3	mutS homolog 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706084
1557363	Msh3	mutS homolog 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1557363	Msh3	mutS homolog 3	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1557363	Msh3	mutS homolog 3	gene	MP:0002957	increased intestinal adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706084
1557363	Msh3	mutS homolog 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1557363	Msh3	mutS homolog 3	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545954
1557363	Msh3	mutS homolog 3	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706084
1557363	Msh3	mutS homolog 3	gene	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545954
1557363	Msh3	mutS homolog 3	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545954
1557363	Msh3	mutS homolog 3	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10706084
1557363	Msh3	mutS homolog 3	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:10545954
1557363	Msh3	mutS homolog 3	gene	MP:0014766	impaired mismatch repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:10706084
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668331
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668331
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175628
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20208559
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175628
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175628
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20208559
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0009111	pancreas hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23175628
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19668331
1557364	Stard13	StAR related lipid transfer domain containing 13	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20208559
1557367	Socs5	suppressor of cytokine signaling 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199163
1557367	Socs5	suppressor of cytokine signaling 5	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17611223
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0010887	pale lung		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0010890	decreased alveolar lamellar body number		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557369	Atp23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20220714	MGI			PMID:35682694
1557371	Sash1	SAM and SH3 domain containing 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1557371	Sash1	SAM and SH3 domain containing 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20240523	MGI			
1557371	Sash1	SAM and SH3 domain containing 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1557371	Sash1	SAM and SH3 domain containing 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1557371	Sash1	SAM and SH3 domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557374	Ino80b	INO80 complex subunit B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1557374	Ino80b	INO80 complex subunit B	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20231207	MGI			
1557377	Rnf114	ring finger protein 114	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20210930	MGI			PMID:34104941
1557377	Rnf114	ring finger protein 114	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1557377	Rnf114	ring finger protein 114	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20210930	MGI			PMID:34104941
1557377	Rnf114	ring finger protein 114	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20210930	MGI			PMID:34104941
1557378	Srsf11	serine and arginine-rich splicing factor 11	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20211021	MGI			
1557378	Srsf11	serine and arginine-rich splicing factor 11	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20211021	MGI			
1557378	Srsf11	serine and arginine-rich splicing factor 11	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1557378	Srsf11	serine and arginine-rich splicing factor 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557378	Srsf11	serine and arginine-rich splicing factor 11	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230601	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230601	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0003236	abnormal lens capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707242
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005161	hematuria		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23707242
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20191212	MGI			PMID:29263159
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0005567	decreased circulating total protein level		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20201224	MGI			PMID:30582011
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011483	renal glomerular synechia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0011509	dilated glomerular capillary		IAGP		N	RGD:5509061	20141003	MGI			PMID:15153557
1557379	Col4a5	collagen, type IV, alpha 5	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20210128	MGI			
1557380	Zpbp	zona pellucida binding protein	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557380	Zpbp	zona pellucida binding protein	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1557381	Map3k9	mitogen-activated protein kinase kinase kinase 9	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1557381	Map3k9	mitogen-activated protein kinase kinase kinase 9	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220811	MGI			
1557381	Map3k9	mitogen-activated protein kinase kinase kinase 9	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20220811	MGI			
1557381	Map3k9	mitogen-activated protein kinase kinase kinase 9	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1557381	Map3k9	mitogen-activated protein kinase kinase kinase 9	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1557381	Map3k9	mitogen-activated protein kinase kinase kinase 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18414056
1557381	Map3k9	mitogen-activated protein kinase kinase kinase 9	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1557381	Map3k9	mitogen-activated protein kinase kinase kinase 9	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000182	increased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20180201	MGI			PMID:24168030
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000198	decreased circulating phosphate level		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20180201	MGI			PMID:24043815
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:19837032
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23303524
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26494787
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20180201	MGI			PMID:25953344
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20180201	MGI			PMID:20040491
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20180201	MGI			PMID:23303524
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20180201	MGI			PMID:26494787
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20180201	MGI			PMID:24043815
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20180201	MGI			PMID:25953344
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20180201	MGI			PMID:26494787
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000316	cellular necrosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:26494787
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:26921005
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20180201	MGI			PMID:25190059
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20180201	MGI			PMID:19060336
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16611729
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20180201	MGI			PMID:16611729
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000566	synostosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:18550708
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000786	abnormal embryonic neuroepithelial layer differentiation		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18509025
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000851	cerebellum hypoplasia		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20180201	MGI			PMID:17619227
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:20573697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:20573697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20180201	MGI			PMID:24043815
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20180201	MGI			PMID:25809849
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20180201	MGI			PMID:22110054
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000932	absent notochord		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000933	abnormal rhombomere morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:25652406
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20180201	MGI			PMID:26921005
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:17619227
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:18509025
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:18509025
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180201	MGI			PMID:25652406
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001289	persistence of hyaloid vascular system		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20180201	MGI			PMID:17619227
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001296	macrophthalmia		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:18509025
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20180201	MGI			PMID:17765677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180201	MGI			PMID:18509025
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20180201	MGI			PMID:17765677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20180201	MGI			PMID:22763239
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20180201	MGI			PMID:17619227
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:18550708
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:19023080
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20180201	MGI			PMID:24043815
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20180201	MGI			PMID:19279185
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21094155
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20180201	MGI			PMID:15302604
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20180201	MGI			PMID:22991437
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20180201	MGI			PMID:15302604
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20180201	MGI			PMID:18171685
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20180201	MGI			PMID:18171685
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20180201	MGI			PMID:20573697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20180201	MGI			PMID:26494787
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23303524
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20180201	MGI			PMID:19830823
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20180201	MGI			PMID:22991437
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180201	MGI			PMID:18550708
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180201	MGI			PMID:20573697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180201	MGI			PMID:20978237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180201	MGI			PMID:26921005
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20180201	MGI			PMID:20040491
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19464366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20978237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19464366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20180201	MGI			PMID:18550708
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20180201	MGI			PMID:20978237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20180201	MGI			PMID:23142660
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20180201	MGI			PMID:17060609
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20180201	MGI			PMID:20978237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20180201	MGI			PMID:22110054
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:25652406
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20180201	MGI			PMID:19279185
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20180201	MGI			PMID:19023080
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:22516201
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20180201	MGI			PMID:25652406
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:18171685
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:24043815
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20180201	MGI			PMID:15302604
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22516201
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22991437
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23142660
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26921005
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16611729
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22516201
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19060336
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23303524
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:19219045
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:19279185
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:22453236
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190207	MGI			PMID:28708136
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002174	abnormal gastrulation movements		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002207	abnormal long-term potentiation		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18171685
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19830823
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18550708
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20180201	MGI			PMID:26219237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17765677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008446
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20180301	MGI			PMID:29097735
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:25953344
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002862	abnormal righting response		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002904	increased circulating parathyroid hormone level		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20180201	MGI			PMID:22763239
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20180201	MGI			PMID:23217742
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0002995	primary sex reversal		IAGP		N	RGD:5509061	20180201	MGI			PMID:23102580
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20180201	MGI			PMID:25809849
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20180531	MGI			PMID:28337978
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003116	rickets		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20180201	MGI			PMID:22110054
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003169	abnormal scala media morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17765677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22110054
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23142660
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20180201	MGI			PMID:20978237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003381	vitreal fibroplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003451	absent olfactory bulb		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003613	abnormal kidney medulla development		IAGP		N	RGD:5509061	20180201	MGI			PMID:19060336
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008446
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20180201	MGI			PMID:25190059
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20180201	MGI			PMID:19279185
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20180201	MGI			PMID:20978237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20181129	MGI			PMID:27505251
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003815	hairless		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20180201	MGI			PMID:26494787
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18171685
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19830823
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20180201	MGI			PMID:26921005
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:19464366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:19837032
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:24043815
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:26494787
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20573697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26494787
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22190642
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20180201	MGI			PMID:26494787
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20180201	MGI			PMID:20040491
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20180201	MGI			PMID:20040491
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23217742
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004323	sternum hypoplasia		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004360	absent ulna		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004476	absent palatine bone		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004559	small allantois		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004575	small limb buds		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004678	split xiphoid process		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20180201	MGI			PMID:22833677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0004887	decreased endolymph production		IAGP		N	RGD:5509061	20180201	MGI			PMID:17765677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005034	abnormal anus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16611729
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20180201	MGI			PMID:25809849
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005167	abnormal blood-brain barrier function		IAGP		N	RGD:5509061	20180201	MGI			PMID:19023080
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20180201	MGI			PMID:24168030
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005313	absent adrenal gland		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005336	abnormal inguinal fat pad morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:25652406
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005547	abnormal Muller cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17639082
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:26921005
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20180201	MGI			PMID:19023080
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006061	right atrial isomerism		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006069	abnormal retina neuronal layer morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006142	abnormal sinoatrial node conduction		IAGP		N	RGD:5509061	20180301	MGI			PMID:29097735
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:19644017
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006359	absent startle reflex		IAGP		N	RGD:5509061	20180201	MGI			PMID:17765677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18550708
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:27505251
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22763239
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008308	small scala media		IAGP		N	RGD:5509061	20180201	MGI			PMID:17765677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008393	absent primordial germ cells		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008488	abnormal semicircular canal ampulla morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:17765677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:19279185
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:20079728
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20180201	MGI			PMID:23142660
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20181129	MGI			PMID:27505251
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008903	abnormal mesenteric fat pad morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008926	abnormal anterior definitive endoderm morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20180201	MGI			PMID:22763239
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:18550708
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009022	abnormal brain meninges morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009026	abnormal brain pia mater morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009130	increased white fat cell number		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009266	abnormal mesendoderm development		IAGP		N	RGD:5509061	20180201	MGI			PMID:20573697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009323	abnormal spleen development		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009331	absent primitive node		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009445	osteomalacia		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23217742
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009573	abnormal right lung middle lobe morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23217742
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009695	abnormal spinal cord ventral commissure morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23217742
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20210422	MGI			PMID:26851218
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20180201	MGI			PMID:17619227
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20180201	MGI			PMID:16611729
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20211021	MGI			PMID:32280065
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008446
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19837032
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009869	abnormal descending aorta morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19837032
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15576405
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22763239
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22110054
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010126	abnormal distal visceral endoderm morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:15302604
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010235	abnormal retina inner limiting membrane morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010387	abnormal Bergmann glial cell morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21983115
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:25953344
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010437	absent coronary sinus		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010736	abnormal extraembryonic ectoderm morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010807	abnormal stomach position or orientation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010853	abnormal lung position or orientation		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0010996	increased aorta wall thickness		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17619227
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:25190059
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:25809849
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210422	MGI			PMID:26851218
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20251127	MGI			PMID:39127888
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:24895408
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210422	MGI			PMID:26851218
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:15576405
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:16611729
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19837032
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:20689803
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:22991437
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:26553930
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200430	MGI			PMID:31950080
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18974357
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:25480920
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:26290337
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:26921005
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20221229	MGI			PMID:29967292
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:17060609
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:16467350
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20210114	MGI			PMID:32702291
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18550708
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19023080
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19279185
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:20040491
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:20978237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:25953344
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19307312
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:21768372
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:23028370
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:23824717
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:26292834
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19464366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19690388
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:19837032
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:20573697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201015	MGI			PMID:32658897
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:18440989
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:23184148
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20180201	MGI			PMID:25809849
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011144	thin lung-associated mesenchyme		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011148	decreased mesenchymal cell proliferation involved in lung development		IAGP		N	RGD:5509061	20180201	MGI			PMID:18367557
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011156	abnormal hypodermis fat layer morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011169	abnormal white fat cell differentation		IAGP		N	RGD:5509061	20180201	MGI			PMID:21664579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:18171685
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011205	excessive folding of visceral yolk sac		IAGP		N	RGD:5509061	20180201	MGI			PMID:20978237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011228	abnormal vitamin D level		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011273	prolonged excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011345	truncated loop of Henle		IAGP		N	RGD:5509061	20180201	MGI			PMID:19060336
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:19060336
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:21768366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011438	absent kidney medulla		IAGP		N	RGD:5509061	20180201	MGI			PMID:19060336
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011439	abnormal kidney cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:19060336
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:19060336
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011504	abnormal limb long bone morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011521	decreased placental labyrinth size		IAGP		N	RGD:5509061	20180201	MGI			PMID:20978237
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20240620	MGI			PMID:38453366
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011843	abnormal kidney collecting duct epithelium morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:19060336
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20180201	MGI			PMID:17765677
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012083	absent foregut		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012083	absent foregut		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012084	truncated foregut		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012086	absent hindgut		IAGP		N	RGD:5509061	20180201	MGI			PMID:15215210
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012091	increased midbrain size		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012136	absent forebrain		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012139	increased forebrain size		IAGP		N	RGD:5509061	20180201	MGI			PMID:17468181
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20180201	MGI			PMID:12842913
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20180201	MGI			PMID:18171685
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22110054
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012175	flat face		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012671	retina spots		IAGP		N	RGD:5509061	20180201	MGI			PMID:20048158
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20180201	MGI			PMID:20040491
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20180201	MGI			PMID:20573697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22383895
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0012724	absent head fold		IAGP		N	RGD:5509061	20240627	MGI			PMID:22669107
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0013140	excessive vocalization		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20180201	MGI			PMID:26921005
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:27179789
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014078	small intestinal villus atrophy		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20180201	MGI			PMID:26232697
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014103	increased chondrocyte apoptosis		IAGP		N	RGD:5509061	20181129	MGI			PMID:27505251
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014104	decreased chondrocyte apoptosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:26921005
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:22763239
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014629	hypothalamus hypoplasia		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20180201	MGI			PMID:22615579
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0020290	floppy ears		IAGP		N	RGD:5509061	20181129	MGI			PMID:27505251
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0020333	enhanced leukocyte tethering or rolling		IAGP		N	RGD:5509061	20160915	MGI			PMID:19008446
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0020391	radial glial endfoot detachment		IAGP		N	RGD:5509061	20180201	MGI			PMID:23217742
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0020528	thalamus hypoplasia		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0030423	abnormal pinna cartilage morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:27505251
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0030538	abnormal notochordal plate morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:21693517
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0030798	joint contracture		IAGP		N	RGD:5509061	20230323	MGI			PMID:34767447
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0031185	sudden unexpected death in epilepsy		IAGP		N	RGD:5509061	20251009	MGI			PMID:40277233
1557383	Edil3	EGF-like repeats and discoidin I-like domains 3	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:24895408
1557386	Cks2	CDC28 protein kinase regulatory subunit 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714746
1557386	Cks2	CDC28 protein kinase regulatory subunit 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714746
1557386	Cks2	CDC28 protein kinase regulatory subunit 2	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714746
1557386	Cks2	CDC28 protein kinase regulatory subunit 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714746
1557386	Cks2	CDC28 protein kinase regulatory subunit 2	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714746
1557386	Cks2	CDC28 protein kinase regulatory subunit 2	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12714746
1557386	Cks2	CDC28 protein kinase regulatory subunit 2	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:12714746
1557387	Zscan5b	zinc finger and SCAN domain containing 5B	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1557387	Zscan5b	zinc finger and SCAN domain containing 5B	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20201022	MGI			
1557387	Zscan5b	zinc finger and SCAN domain containing 5B	gene	MP:0010095	increased chromosomal stability		IAGP		N	RGD:5509061	20201001	MGI			PMID:31155506
1557390	Pof1b	premature ovarian failure 1B	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20221215	MGI			
1557390	Pof1b	premature ovarian failure 1B	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1557390	Pof1b	premature ovarian failure 1B	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1557390	Pof1b	premature ovarian failure 1B	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1557390	Pof1b	premature ovarian failure 1B	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1557390	Pof1b	premature ovarian failure 1B	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557390	Pof1b	premature ovarian failure 1B	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1557391	Spata16	spermatogenesis associated 16	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557391	Spata16	spermatogenesis associated 16	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557391	Spata16	spermatogenesis associated 16	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557391	Spata16	spermatogenesis associated 16	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557391	Spata16	spermatogenesis associated 16	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557391	Spata16	spermatogenesis associated 16	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557391	Spata16	spermatogenesis associated 16	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557391	Spata16	spermatogenesis associated 16	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557391	Spata16	spermatogenesis associated 16	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557391	Spata16	spermatogenesis associated 16	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20180705	MGI			PMID:29065458
1557392	Hsfy2	heat shock transcription factor, Y-linked 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1557392	Hsfy2	heat shock transcription factor, Y-linked 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220519	MGI			
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0001512	trunk curl		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:29078393
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0004146	absent M line		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20161013	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:29078393
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180614	MGI			PMID:29078393
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20160128	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0014730	abnormal myocardial fiber myofibril morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0014921	decreased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0014921	decreased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:29078393
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:26487682
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0031709	ventricular arrhythmia		IAGP		N	RGD:5509061	20260514	MGI			PMID:27274810
1557393	Lmod2	leiomodin 2 (cardiac)	gene	MP:0031717	prolonged corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:27274810
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0000162	lordosis		IEA		N	RGD:5509061	20250508	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230119	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199160
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0003080	increased natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15199160
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0003080	increased natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439675
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0003080	increased natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203684
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20230119	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0004819	decreased skeletal muscle mass		IEA		N	RGD:5509061	20230119	MGI			
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203684
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439675
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203684
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439675
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203684
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18203684
1557394	Clnk	cytokine-dependent hematopoietic cell linker	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16439675
1557395	Snx12	sorting nexin 12	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557395	Snx12	sorting nexin 12	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20220811	MGI			
1557395	Snx12	sorting nexin 12	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557397	Lcor	ligand dependent nuclear receptor corepressor	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20260514	MGI			PMID:41785858
1557397	Lcor	ligand dependent nuclear receptor corepressor	gene	MP:0004644	increased vertebrae number		IAGP		N	RGD:5509061	20260514	MGI			PMID:41785858
1557397	Lcor	ligand dependent nuclear receptor corepressor	gene	MP:0004651	increased thoracic vertebrae number		IAGP		N	RGD:5509061	20260514	MGI			PMID:41785858
1557397	Lcor	ligand dependent nuclear receptor corepressor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200514	MGI			PMID:29628311
1557398	Tm2d3	TM2 domain containing 3	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20210128	MGI			
1557398	Tm2d3	TM2 domain containing 3	gene	MP:0001785	edema		IEA		N	RGD:5509061	20220519	MGI			
1557398	Tm2d3	TM2 domain containing 3	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20220519	MGI			
1557398	Tm2d3	TM2 domain containing 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1557398	Tm2d3	TM2 domain containing 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557398	Tm2d3	TM2 domain containing 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557399	Acot4	acyl-CoA thioesterase 4	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1557400	Dhrs7	dehydrogenase/reductase 7	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1557402	Vit	vitrin	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20170223	MGI			PMID:25331329
1557402	Vit	vitrin	gene	MP:0000956	decreased spinal cord size		IAGP		N	RGD:5509061	20170223	MGI			PMID:25331329
1557402	Vit	vitrin	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:25331329
1557402	Vit	vitrin	gene	MP:0004100	abnormal spinal cord interneuron morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:25331329
1557402	Vit	vitrin	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20170223	MGI			PMID:25331329
1557402	Vit	vitrin	gene	MP:0009688	abnormal spinal cord central canal morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:25331329
1557402	Vit	vitrin	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20170223	MGI			PMID:25331329
1557402	Vit	vitrin	gene	MP:0010151	abnormal spinal cord ependymal layer morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:25331329
1557402	Vit	vitrin	gene	MP:0012203	abnormal neuronal stem cell morphology		IAGP		N	RGD:5509061	20170223	MGI			PMID:25331329
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0003976	decreased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0010360	decreased liver free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:22231784
1557405	Naa40	N(alpha)-acetyltransferase 40, NatD catalytic subunit	gene	MP:0031270	decreased susceptibility to age-related hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:22231784
1557406	Dct	dopachrome tautomerase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:15060160
1557406	Dct	dopachrome tautomerase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:18715234
1557406	Dct	dopachrome tautomerase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:8530099
1557406	Dct	dopachrome tautomerase	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20211223	MGI			PMID:33100333
1557406	Dct	dopachrome tautomerase	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1557406	Dct	dopachrome tautomerase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1557406	Dct	dopachrome tautomerase	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20181122	MGI			PMID:20144786
1557406	Dct	dopachrome tautomerase	gene	MP:0002939	head spot		IAGP		N	RGD:5509061	20181122	MGI			PMID:25818501
1557406	Dct	dopachrome tautomerase	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20181122	MGI			PMID:20144786
1557406	Dct	dopachrome tautomerase	gene	MP:0005102	abnormal iris pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18715234
1557406	Dct	dopachrome tautomerase	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20211223	MGI			PMID:33100333
1557406	Dct	dopachrome tautomerase	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20211021	MGI			
1557406	Dct	dopachrome tautomerase	gene	MP:0010037	ectopic melanocytes		IAGP		N	RGD:5509061	20181122	MGI			PMID:20144786
1557406	Dct	dopachrome tautomerase	gene	MP:0010192	abnormal retina melanin granule morphology		IAGP		N	RGD:5509061	20211223	MGI			PMID:33100333
1557406	Dct	dopachrome tautomerase	gene	MP:0010206	pigment incontinence		IAGP		N	RGD:5509061	20181129	MGI			PMID:20144786
1557406	Dct	dopachrome tautomerase	gene	MP:0011830	ectopic hair follicle melanin granules		IAGP		N	RGD:5509061	20181122	MGI			PMID:20144786
1557407	Zbtb33	zinc finger and BTB domain containing 33	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354691
1557407	Zbtb33	zinc finger and BTB domain containing 33	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354691
1557407	Zbtb33	zinc finger and BTB domain containing 33	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354691
1557407	Zbtb33	zinc finger and BTB domain containing 33	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16354691
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20250508	MGI			
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20250508	MGI			
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16166649
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20250508	MGI			
1557408	G3bp1	G3BP stress granule assembly factor 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1557409	Cbx3	chromobox 3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20423503
1557409	Cbx3	chromobox 3	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20423503
1557409	Cbx3	chromobox 3	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17644066
1557409	Cbx3	chromobox 3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20423503
1557409	Cbx3	chromobox 3	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20423503
1557409	Cbx3	chromobox 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20423503
1557409	Cbx3	chromobox 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20423503
1557411	Ppp6r2	protein phosphatase 6, regulatory subunit 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141218	MGI			PMID:24440290
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24440290
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0010927	decreased osteoid volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0010930	decreased osteoid thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20250605	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21071677
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:19884350
1557413	Naca	nascent polypeptide-associated complex alpha polypeptide	gene	MP:0030482	increased osteocyte number		IAGP		N	RGD:5509061	20171221	MGI			PMID:19884350
1557414	Ubqln2	ubiquilin 2	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20260730	MGI			PMID:27477512
1557414	Ubqln2	ubiquilin 2	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20260730	MGI			PMID:27477512
1557414	Ubqln2	ubiquilin 2	gene	MP:0014062	nervous system inclusion bodies		IAGP		N	RGD:5509061	20260730	MGI			PMID:27477512
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807825
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16557300
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16987502
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16987502
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16987502
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:11901205
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16987502
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994431
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807825
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994431
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807825
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0005327	abnormal mesangial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16987502
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16987502
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008343	abnormal gamma-delta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994431
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994431
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0009544	abnormal thymus epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21441458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0009628	absent brachial lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0009634	absent popliteal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12070288
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0013588	small thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:21441458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20220519	MGI			PMID:29178458
1557415	Tnfsf14	tumor necrosis factor (ligand) superfamily, member 14	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:16987502
1557416	Myof	myoferlin	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1557416	Myof	myoferlin	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16280346
1557416	Myof	myoferlin	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16280346
1557416	Myof	myoferlin	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20250508	MGI			
1557416	Myof	myoferlin	gene	MP:0003071	decreased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:17702744
1557416	Myof	myoferlin	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16280346
1557416	Myof	myoferlin	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20250508	MGI			
1557416	Myof	myoferlin	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20250508	MGI			
1557416	Myof	myoferlin	gene	MP:0009408	decreased skeletal muscle fiber density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16280346
1557416	Myof	myoferlin	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16280346
1557417	Gdf3	growth differentiation factor 3	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1557417	Gdf3	growth differentiation factor 3	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0001687	thin endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008465
1557417	Gdf3	growth differentiation factor 3	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1557417	Gdf3	growth differentiation factor 3	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1557417	Gdf3	growth differentiation factor 3	gene	MP:0004713	split notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008465
1557417	Gdf3	growth differentiation factor 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008465
1557417	Gdf3	growth differentiation factor 3	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1557417	Gdf3	growth differentiation factor 3	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008465
1557417	Gdf3	growth differentiation factor 3	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008465
1557417	Gdf3	growth differentiation factor 3	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008465
1557417	Gdf3	growth differentiation factor 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19008465
1557417	Gdf3	growth differentiation factor 3	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1557417	Gdf3	growth differentiation factor 3	gene	MP:0011255	abnormal anterior visceral endoderm cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0011255	abnormal anterior visceral endoderm cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1557417	Gdf3	growth differentiation factor 3	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0012156	rostral-caudal axis duplication		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557417	Gdf3	growth differentiation factor 3	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1557417	Gdf3	growth differentiation factor 3	gene	MP:0012159	absent anterior visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1557417	Gdf3	growth differentiation factor 3	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17936261
1557417	Gdf3	growth differentiation factor 3	gene	MP:0013207	absent endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:16368929
1557418	Gpihbp1	GPI-anchored HDL-binding protein 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403372
1557418	Gpihbp1	GPI-anchored HDL-binding protein 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403372
1557418	Gpihbp1	GPI-anchored HDL-binding protein 1	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403372
1557418	Gpihbp1	GPI-anchored HDL-binding protein 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17403372
1557419	Col24a1	collagen, type XXIV, alpha 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1557419	Col24a1	collagen, type XXIV, alpha 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20160421	MGI			
1557421	Asb10	ankyrin repeat and SOCS box-containing 10	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1557421	Asb10	ankyrin repeat and SOCS box-containing 10	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1557421	Asb10	ankyrin repeat and SOCS box-containing 10	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1557422	Serpinb12	serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 12	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20170105	MGI			
1557422	Serpinb12	serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 12	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12572850
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001296	macrophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12572850
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12572850
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002832	coarse hair		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:22847837
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12572850
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002936	joint swelling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12572850
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0002997	enlarged seminal vesicle		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20201217	MGI			PMID:22847837
1557423	Ids	iduronate 2-sulfatase	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0004288	abnormal spiral ligament morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:22847837
1557423	Ids	iduronate 2-sulfatase	gene	MP:0004308	abnormal basilar membrane morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:22847837
1557423	Ids	iduronate 2-sulfatase	gene	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0004928	increased epididymis weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12572850
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005503	abnormal tendon morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0006018	abnormal tympanic membrane morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:22847837
1557423	Ids	iduronate 2-sulfatase	gene	MP:0006021	abnormal Reissner membrane morphology		IAGP		N	RGD:5509061	20201217	MGI			PMID:22847837
1557423	Ids	iduronate 2-sulfatase	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:16505002
1557423	Ids	iduronate 2-sulfatase	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0009728	abnormal calcaneum morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0009840	abnormal foam cell morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0009877	exostosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20201217	MGI			PMID:22847837
1557423	Ids	iduronate 2-sulfatase	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20201217	MGI			PMID:22847837
1557423	Ids	iduronate 2-sulfatase	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0020169	increased thyroid gland weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030068	large face		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030074	coarse facial features		IAGP		N	RGD:5509061	20170921	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030074	coarse facial features		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030188	round snout		IAGP		N	RGD:5509061	20180118	MGI			PMID:22704483
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030316	enlarged neurocranium		IAGP		N	RGD:5509061	20180927	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030410	middle ear effusion		IAGP		N	RGD:5509061	20201217	MGI			PMID:22847837
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030776	calcified calcaneal tendon		IAGP		N	RGD:5509061	20181004	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030808	abnormal hindlimb joint morphology		IAGP		N	RGD:5509061	20181101	MGI			PMID:17876721
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030808	abnormal hindlimb joint morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030811	abnormal hand joint morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:20652491
1557423	Ids	iduronate 2-sulfatase	gene	MP:0030863	decreased joint mobility		IAGP		N	RGD:5509061	20181101	MGI			PMID:17876721
1557424	Arx	aristaless related homeobox	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14561778
1557424	Arx	aristaless related homeobox	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0000743	muscle spasm		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14561778
1557424	Arx	aristaless related homeobox	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18799476
1557424	Arx	aristaless related homeobox	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18799476
1557424	Arx	aristaless related homeobox	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18799476
1557424	Arx	aristaless related homeobox	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14561778
1557424	Arx	aristaless related homeobox	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1557424	Arx	aristaless related homeobox	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14561778
1557424	Arx	aristaless related homeobox	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18799476
1557424	Arx	aristaless related homeobox	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0002826	tonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0003246	loss of GABAergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0003247	abnormal glutaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22056672
1557424	Arx	aristaless related homeobox	gene	MP:0003460	decreased fear-related response		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0003645	increased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14561778
1557424	Arx	aristaless related homeobox	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0003996	clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0003996	clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0004103	abnormal ventral striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0005148	seminal vesicle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0005218	abnormal pancreatic delta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14561778
1557424	Arx	aristaless related homeobox	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0006308	enlarged seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0008269	abnormal hippocampus CA4 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0008840	abnormal spike wave discharge		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0008929	abnormal central medial nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0009178	absent pancreatic alpha cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:14561778
1557424	Arx	aristaless related homeobox	gene	MP:0009180	increased pancreatic delta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14561778
1557424	Arx	aristaless related homeobox	gene	MP:0009324	absent hippocampal fimbria		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20180913	MGI			PMID:29659809
1557424	Arx	aristaless related homeobox	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19587282
1557424	Arx	aristaless related homeobox	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14561778
1557424	Arx	aristaless related homeobox	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0013603	abnormal fetal Leydig cell differentiation		IAGP		N	RGD:5509061	20150319	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0014551	impaired neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0014558	decreased cortical ventricular zone thickness		IAGP		N	RGD:5509061	20241031	MGI			PMID:12379852
1557424	Arx	aristaless related homeobox	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0014624	abnormal brain delta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:19439424
1557424	Arx	aristaless related homeobox	gene	MP:0015017	decreased cholinergic neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:19605412
1557424	Arx	aristaless related homeobox	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20180913	MGI			PMID:28602636
1557424	Arx	aristaless related homeobox	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:29659809
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294946
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294946
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294946
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228330
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0002491	decreased IgD level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294946
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228330
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15368291
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:15368291
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973390
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294946
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15368291
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782029
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17073941
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008183	absent marginal zone B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294946
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228330
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294946
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17420268
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18663224
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228330
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008216	absent transitional stage B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294946
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300983
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294946
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15294936
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15368291
1557427	Tnfrsf13c	tumor necrosis factor receptor superfamily, member 13c	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21228330
1557428	Enox2	ecto-NOX disulfide-thiol exchanger 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557429	Cd209e	CD209e antigen	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1557430	Glt8d2	glycosyltransferase 8 domain containing 2	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1557430	Glt8d2	glycosyltransferase 8 domain containing 2	gene	MP:0002420	abnormal adaptive immunity		IEA		N	RGD:5509061	20170413	MGI			
1557430	Glt8d2	glycosyltransferase 8 domain containing 2	gene	MP:0008495	decreased IgG1 level		IEA		N	RGD:5509061	20170413	MGI			
1557430	Glt8d2	glycosyltransferase 8 domain containing 2	gene	MP:0008496	decreased IgG2a level		IEA		N	RGD:5509061	20170413	MGI			
1557430	Glt8d2	glycosyltransferase 8 domain containing 2	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1557430	Glt8d2	glycosyltransferase 8 domain containing 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20150430	MGI			
1557431	Sertad2	SERTA domain containing 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0003953	abnormal hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0004892	increased adiponectin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0005418	abnormal circulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0005459	decreased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0009127	increased brown fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0009136	decreased brown fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0011016	increased core body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16721052
1557431	Sertad2	SERTA domain containing 2	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20160414	MGI			PMID:23291629
1557431	Sertad2	SERTA domain containing 2	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:23291629
1557432	Pdk3	pyruvate dehydrogenase kinase, isoenzyme 3	gene	MP:0002575	increased circulating ketone body level		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1557432	Pdk3	pyruvate dehydrogenase kinase, isoenzyme 3	gene	MP:0005416	abnormal circulating protein level		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1557432	Pdk3	pyruvate dehydrogenase kinase, isoenzyme 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1557432	Pdk3	pyruvate dehydrogenase kinase, isoenzyme 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1557432	Pdk3	pyruvate dehydrogenase kinase, isoenzyme 3	gene	MP:0013404	decreased circulating lactate level		IAGP		N	RGD:5509061	20210610	MGI			PMID:33773101
1557434	Hopx	HOP homeobox	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0000275	heart hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557434	Hopx	HOP homeobox	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557434	Hopx	HOP homeobox	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557434	Hopx	HOP homeobox	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297045
1557434	Hopx	HOP homeobox	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790958
1557434	Hopx	HOP homeobox	gene	MP:0003567	abnormal fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297045
1557434	Hopx	HOP homeobox	gene	MP:0004071	prolonged P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790958
1557434	Hopx	HOP homeobox	gene	MP:0004072	abnormal frontal plane axis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790958
1557434	Hopx	HOP homeobox	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297045
1557434	Hopx	HOP homeobox	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297045
1557434	Hopx	HOP homeobox	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12975471
1557434	Hopx	HOP homeobox	gene	MP:0005586	decreased tidal volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557434	Hopx	HOP homeobox	gene	MP:0006027	impaired lung alveolus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557434	Hopx	HOP homeobox	gene	MP:0006321	increased myocardial fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12975471
1557434	Hopx	HOP homeobox	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790958
1557434	Hopx	HOP homeobox	gene	MP:0010553	prolonged HV interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790958
1557434	Hopx	HOP homeobox	gene	MP:0010560	intraventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:15790958
1557434	Hopx	HOP homeobox	gene	MP:0010992	increased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557434	Hopx	HOP homeobox	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557434	Hopx	HOP homeobox	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557434	Hopx	HOP homeobox	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297045
1557434	Hopx	HOP homeobox	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12297046
1557434	Hopx	HOP homeobox	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12975471
1557434	Hopx	HOP homeobox	gene	MP:0011142	abnormal lung-associated mesenchyme development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557434	Hopx	HOP homeobox	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:16510470
1557436	Mob2	MOB kinase activator 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1557436	Mob2	MOB kinase activator 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557438	Cpvl	carboxypeptidase, vitellogenic-like	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1557438	Cpvl	carboxypeptidase, vitellogenic-like	gene	MP:0001200	thick skin		IEA		N	RGD:5509061	20181227	MGI			
1557438	Cpvl	carboxypeptidase, vitellogenic-like	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1557438	Cpvl	carboxypeptidase, vitellogenic-like	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1557438	Cpvl	carboxypeptidase, vitellogenic-like	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19884347
1557444	Akap17b	A kinase anchor protein 17B	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20111116	MGI			
1557444	Akap17b	A kinase anchor protein 17B	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20111116	MGI			
1557444	Akap17b	A kinase anchor protein 17B	gene	MP:0002084	abnormal developmental patterning		IEA		N	RGD:5509061	20111116	MGI			
1557444	Akap17b	A kinase anchor protein 17B	gene	MP:0002085	abnormal embryonic tissue morphology		IEA		N	RGD:5509061	20111116	MGI			
1557444	Akap17b	A kinase anchor protein 17B	gene	MP:0003400	kinked neural tube		IEA		N	RGD:5509061	20111116	MGI			
1557444	Akap17b	A kinase anchor protein 17B	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1557444	Akap17b	A kinase anchor protein 17B	gene	MP:0009657	failure of chorioallantoic fusion		IEA		N	RGD:5509061	20111116	MGI			
1557444	Akap17b	A kinase anchor protein 17B	gene	MP:0009768	impaired somite development		IEA		N	RGD:5509061	20111116	MGI			
1557444	Akap17b	A kinase anchor protein 17B	gene	MP:0011732	decreased somite size		IEA		N	RGD:5509061	20141003	MGI			
1557445	Prkx	protein kinase, X-linked	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1557446	Klhl42	kelch-like 42	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1557446	Klhl42	kelch-like 42	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20181227	MGI			
1557446	Klhl42	kelch-like 42	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000688	lymphoid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917799
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917799
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917799
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917799
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917799
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917799
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917799
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15917799
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008522	abnormal lymph node germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0008895	abnormal intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0009481	cecum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23451046
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583643
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0010189	abnormal T follicular helper cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22700722
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23583642
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21844204
1557447	Rc3h1	RING CCCH (C3H) domains 1	gene	MP:0031301	chronic liver inflammation		IAGP		N	RGD:5509061	20211028	MGI			PMID:23451046
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20230119	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615047
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20230119	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230119	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615047
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615047
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615047
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615047
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230119	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001785	edema		IEA		N	RGD:5509061	20230119	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615047
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008285	abnormal hippocampus granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008442	disorganized cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008443	absent subplate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008444	retina cone cell degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008449	abnormal retina cone cell outer segment morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008456	abnormal retina rod cell outer segment morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0010236	abnormal retina outer limiting membrane morphology		IAGP		N	RGD:5509061	20200109	MGI			PMID:28370415
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615047
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12773624
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20230601	MGI			
1557448	Top2b	topoisomerase (DNA) II beta	gene	MP:0014551	impaired neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:12773624
1557451	Strip1	striatin interacting protein 1	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557451	Strip1	striatin interacting protein 1	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557451	Strip1	striatin interacting protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557451	Strip1	striatin interacting protein 1	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557451	Strip1	striatin interacting protein 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557451	Strip1	striatin interacting protein 1	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557451	Strip1	striatin interacting protein 1	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557451	Strip1	striatin interacting protein 1	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557451	Strip1	striatin interacting protein 1	gene	MP:0012173	short rostral-caudal axis		IAGP		N	RGD:5509061	20180329	MGI			PMID:29203676
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0010227	decreased quadriceps weight		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20230601	MGI			
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20190221	MGI			PMID:23812712
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557452	Cox7a2l	cytochrome c oxidase subunit 7A2 like	gene	MP:0020520	whitened brown adipose tissue morphology		IAGP		N	RGD:5509061	20200130	MGI			PMID:23857330
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20181227	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20181227	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20181227	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20181227	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20241121	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20181227	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20181227	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0003720	abnormal neural tube closure		IEA		N	RGD:5509061	20181227	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20181227	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0006001	abnormal intestinal transit time		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557454	Pcgf1	polycomb group ring finger 1	gene	MP:0014484	decreased feces water content		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557455	Hoxa7	homeobox A7	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784603
1557455	Hoxa7	homeobox A7	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784603
1557455	Hoxa7	homeobox A7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9784603
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20211021	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1557457	Kbtbd8	kelch repeat and BTB (POZ) domain containing 8	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1557459	Noto	notochord homeobox	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357932
1557459	Noto	notochord homeobox	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231714
1557459	Noto	notochord homeobox	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720144
1557459	Noto	notochord homeobox	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357932
1557459	Noto	notochord homeobox	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231714
1557459	Noto	notochord homeobox	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357932
1557459	Noto	notochord homeobox	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231714
1557459	Noto	notochord homeobox	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720144
1557459	Noto	notochord homeobox	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720144
1557459	Noto	notochord homeobox	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720144
1557459	Noto	notochord homeobox	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357932
1557459	Noto	notochord homeobox	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357932
1557459	Noto	notochord homeobox	gene	MP:0004612	fusion of vertebral bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0004645	decreased vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231714
1557459	Noto	notochord homeobox	gene	MP:0004645	decreased vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8155581
1557459	Noto	notochord homeobox	gene	MP:0004647	decreased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0004714	truncated notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0004714	truncated notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:15231714
1557459	Noto	notochord homeobox	gene	MP:0004714	truncated notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:15550757
1557459	Noto	notochord homeobox	gene	MP:0004714	truncated notochord		IAGP		N	RGD:5509061	20141003	MGI			PMID:8155581
1557459	Noto	notochord homeobox	gene	MP:0006029	abnormal sclerotome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13837681
1557459	Noto	notochord homeobox	gene	MP:0008933	abnormal motile primary cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357932
1557459	Noto	notochord homeobox	gene	MP:0011998	decreased embryonic cilium length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357932
1557459	Noto	notochord homeobox	gene	MP:0012027	abnormal embryonic cilium location or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357932
1557459	Noto	notochord homeobox	gene	MP:0012093	absent nodal flow		IAGP		N	RGD:5509061	20141003	MGI			PMID:22357932
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20161201	MGI			
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20151217	MGI			PMID:24492962
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20151217	MGI			PMID:24492962
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008122	decreased myeloid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20151217	MGI			PMID:24492962
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008188	abnormal transitional stage B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0010228	decreased transitional stage T3 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267016
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0010675	decreased activation-induced B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23267013
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:23267015
1557460	Sppl2a	signal peptide peptidase like 2A	gene	MP:0020001	decreased response to antigen		IEA		N	RGD:5509061	20161201	MGI			
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000754	paresis		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000964	small dorsal root ganglion		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0001664	abnormal digestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25030553
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0003484	abnormal channel response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0005408	hypopigmentation		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20201022	MGI			
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0008812	abnormal rostrocaudal coat patterning		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0009543	abnormal thymus corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0010093	decreased circulating magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18974357
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0011436	decreased urine magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0011979	abnormal magnesium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0012023	decreased melanocyte number		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0012024	abnormal nephron morphogenesis		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0012025	abnormal comma shaped body morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0012026	abnormal S-shaped body morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0012367	decreased erythrocyte magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21045827
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557461	Trpm7	transient receptor potential cation channel, subfamily M, member 7	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20181115	MGI			PMID:22203997
1557464	Cers6	ceramide synthase 6	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760501
1557464	Cers6	ceramide synthase 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760501
1557464	Cers6	ceramide synthase 6	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760501
1557464	Cers6	ceramide synthase 6	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760501
1557464	Cers6	ceramide synthase 6	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760501
1557464	Cers6	ceramide synthase 6	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0008912	nervous		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760501
1557464	Cers6	ceramide synthase 6	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760501
1557464	Cers6	ceramide synthase 6	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23760501
1557464	Cers6	ceramide synthase 6	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20150101	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20160421	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0014911	increased fat cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:25295788
1557464	Cers6	ceramide synthase 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:23760501
1557465	Dzip3	DAZ interacting protein 3, zinc finger	gene	MP:0008762	embryonic lethality		IEA		N	RGD:5509061	20141003	MGI			
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10736201
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14627719
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000906	abnormal trigeminal V mesencephalic nucleus morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000910	small facial motor nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000910	small facial motor nucleus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704382
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133851
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001008	abnormal sympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001034	abnormal parasympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001034	abnormal parasympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001034	abnormal parasympathetic ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133851
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001044	abnormal enteric nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001045	abnormal enteric ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704382
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001066	absent trigeminal nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704382
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001071	abnormal facial nerve morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704382
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001074	abnormal vagus nerve morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14627719
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001082	abnormal geniculate ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14627719
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001084	abnormal petrosal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14627719
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001086	absent petrosal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133851
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001087	abnormal nodose ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14627719
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001093	small trigeminal ganglion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001096	abnormal glossopharyngeal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001100	abnormal vagus ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940179
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198276
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001942	abnormal lung volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198276
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198276
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940179
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198276
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198276
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0001957	apnea		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198276
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940179
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002321	hypoventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198276
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900566
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002338	abnormal pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14627719
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002546	mydriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002546	mydriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150159
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002751	abnormal autonomic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003029	alkalemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900566
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003437	abnormal carotid body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14627719
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940179
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10736201
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10360575
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10736201
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0003964	abnormal noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0004002	abnormal jejunum morphology		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198276
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0004186	abnormal area postrema morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14627719
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0004561	absent facial nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:10704382
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940179
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0004990	abnormal ciliary ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150159
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0005576	decreased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14627719
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0005576	decreased pulmonary ventilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900566
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0006001	abnormal intestinal transit time		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0006243	impaired pupillary reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:15150159
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0006276	abnormal autonomic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900566
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0008314	abnormal pterygopalatine ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133851
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940179
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940179
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18198276
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900566
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16319924
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19940179
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10736201
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10736201
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011406	abnormal retrotrapezoid nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133877
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011406	abnormal retrotrapezoid nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900566
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011406	abnormal retrotrapezoid nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011406	abnormal retrotrapezoid nucleus morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:25975378
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0013002	decreased enteric neural crest cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0013005	decreased enteric neural crest cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0013006	abnormal enteric neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22922260
1557466	Phox2b	paired-like homeobox 2b	gene	MP:0014484	decreased feces water content		IAGP		N	RGD:5509061	20241017	MGI			PMID:37452641
1557467	Prdm2	PR domain containing 2, with ZNF domain	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544182
1557467	Prdm2	PR domain containing 2, with ZNF domain	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544182
1557467	Prdm2	PR domain containing 2, with ZNF domain	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544182
1557467	Prdm2	PR domain containing 2, with ZNF domain	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544182
1557467	Prdm2	PR domain containing 2, with ZNF domain	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544182
1557467	Prdm2	PR domain containing 2, with ZNF domain	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544182
1557467	Prdm2	PR domain containing 2, with ZNF domain	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11544182
1557468	Dcaf6	DDB1 and CUL4 associated factor 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20191114	MGI			PMID:26430214
1557468	Dcaf6	DDB1 and CUL4 associated factor 6	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20191114	MGI			PMID:26430214
1557468	Dcaf6	DDB1 and CUL4 associated factor 6	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20191114	MGI			PMID:26430214
1557468	Dcaf6	DDB1 and CUL4 associated factor 6	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20191114	MGI			PMID:26430214
1557468	Dcaf6	DDB1 and CUL4 associated factor 6	gene	MP:0031328	delayed skeletal muscle regeneration		IAGP		N	RGD:5509061	20220106	MGI			PMID:26430214
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226483
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226483
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17306571
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17306571
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0003634	abnormal glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15932596
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226483
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17306571
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17306571
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15932596
1557469	Ptpn13	protein tyrosine phosphatase, non-receptor type 13	gene	MP:0008090	increased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19107198
1557471	Atpsckmt	ATP synthase C subunit lysine N-methyltransferase	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20240328	MGI			PMID:37944527
1557471	Atpsckmt	ATP synthase C subunit lysine N-methyltransferase	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20240328	MGI			PMID:37944527
1557471	Atpsckmt	ATP synthase C subunit lysine N-methyltransferase	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20240328	MGI			PMID:37944527
1557471	Atpsckmt	ATP synthase C subunit lysine N-methyltransferase	gene	MP:0020879	abnormal calcium level		IAGP		N	RGD:5509061	20240328	MGI			PMID:37944527
1557471	Atpsckmt	ATP synthase C subunit lysine N-methyltransferase	gene	MP:0020955	increased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20240328	MGI			PMID:37944527
1557473	Myo6	myosin VI	gene	MP:0000032	cochlear degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1557473	Myo6	myosin VI	gene	MP:0000042	abnormal organ of Corti morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966030
1557473	Myo6	myosin VI	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0000043	organ of Corti degeneration		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0000044	absent organ of Corti		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20200514	MGI			
1557473	Myo6	myosin VI	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20220519	MGI			
1557473	Myo6	myosin VI	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1557473	Myo6	myosin VI	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20220519	MGI			
1557473	Myo6	myosin VI	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20220519	MGI			
1557473	Myo6	myosin VI	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1557473	Myo6	myosin VI	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966030
1557473	Myo6	myosin VI	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20201022	MGI			
1557473	Myo6	myosin VI	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15978262
1557473	Myo6	myosin VI	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1557473	Myo6	myosin VI	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1557473	Myo6	myosin VI	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:20923982
1557473	Myo6	myosin VI	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1557473	Myo6	myosin VI	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15978262
1557473	Myo6	myosin VI	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20200514	MGI			
1557473	Myo6	myosin VI	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1557473	Myo6	myosin VI	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1557473	Myo6	myosin VI	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1557473	Myo6	myosin VI	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1557473	Myo6	myosin VI	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1557473	Myo6	myosin VI	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220519	MGI			
1557473	Myo6	myosin VI	gene	MP:0002730	head shaking		IEA		N	RGD:5509061	20111116	MGI			
1557473	Myo6	myosin VI	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0002895	abnormal otolithic membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220519	MGI			
1557473	Myo6	myosin VI	gene	MP:0003150	detached tectorial membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0003896	prolonged PR interval		IEA		N	RGD:5509061	20241121	MGI			
1557473	Myo6	myosin VI	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20200514	MGI			
1557473	Myo6	myosin VI	gene	MP:0004298	vestibular ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0004324	vestibular hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0004328	decreased vestibular hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0004331	vestibular saccular macula degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0004334	utricular macular degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0004363	stria vascularis degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0004409	abnormal crista ampullaris neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0004416	absent cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0004516	fused vestibular hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966030
1557473	Myo6	myosin VI	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1557473	Myo6	myosin VI	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0004522	abnormal orientation of cochlear hair cell stereociliary bundles		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0004523	decreased cochlear hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1557473	Myo6	myosin VI	gene	MP:0004523	decreased cochlear hair cell stereocilia number		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0004524	short cochlear hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966030
1557473	Myo6	myosin VI	gene	MP:0004528	fused outer hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10525338
1557473	Myo6	myosin VI	gene	MP:0004528	fused outer hair cell stereocilia		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0004528	fused outer hair cell stereocilia		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0004533	fused inner hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10525338
1557473	Myo6	myosin VI	gene	MP:0004533	fused inner hair cell stereocilia		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0004533	fused inner hair cell stereocilia		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0004533	fused inner hair cell stereocilia		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0004534	decreased inner hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0004589	abnormal cochlear hair cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0004738	abnormal auditory brainstem response		IAGP		N	RGD:5509061	20250814	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0004742	abnormal vestibular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966030
1557473	Myo6	myosin VI	gene	MP:0004813	absent linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1557473	Myo6	myosin VI	gene	MP:0004814	reduced linear vestibular evoked potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:16235133
1557473	Myo6	myosin VI	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20200514	MGI			
1557473	Myo6	myosin VI	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:20923982
1557473	Myo6	myosin VI	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:7493015
1557473	Myo6	myosin VI	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1557473	Myo6	myosin VI	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15978262
1557473	Myo6	myosin VI	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20220519	MGI			
1557473	Myo6	myosin VI	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220519	MGI			
1557473	Myo6	myosin VI	gene	MP:0010015	abnormal cuticular plate morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20200514	MGI			
1557473	Myo6	myosin VI	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557473	Myo6	myosin VI	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20200514	MGI			
1557473	Myo6	myosin VI	gene	MP:0010323	retropulsion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10900098
1557473	Myo6	myosin VI	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20210128	MGI			
1557473	Myo6	myosin VI	gene	MP:0011060	abnormal kinocilium morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:28832620
1557473	Myo6	myosin VI	gene	MP:0011062	abnormal outer hair cell kinocilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5980120
1557473	Myo6	myosin VI	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1557473	Myo6	myosin VI	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17329413
1557473	Myo6	myosin VI	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23485424
1557473	Myo6	myosin VI	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20180621	MGI			PMID:20224170
1557473	Myo6	myosin VI	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20200618	MGI			PMID:31103816
1557473	Myo6	myosin VI	gene	MP:0020084	short ears		IEA		N	RGD:5509061	20170914	MGI			
1557474	Zdhhc24	zinc finger, DHHC domain containing 24	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1557474	Zdhhc24	zinc finger, DHHC domain containing 24	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1557475	Hecw2	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:25555806
1557475	Hecw2	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210722	MGI			PMID:25555806
1557475	Hecw2	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210722	MGI			PMID:25555806
1557475	Hecw2	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0009854	impaired gastric peristalsis		IAGP		N	RGD:5509061	20210722	MGI			PMID:25555806
1557475	Hecw2	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0010801	abnormal myenteric nerve plexus morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:25555806
1557475	Hecw2	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210722	MGI			PMID:25555806
1557475	Hecw2	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557475	Hecw2	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0013958	decreased small intestine length		IAGP		N	RGD:5509061	20210722	MGI			PMID:25555806
1557475	Hecw2	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20210722	MGI			PMID:25555806
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669417
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0001985	abnormal gustatory system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12581520
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0001986	abnormal taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12581520
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20160623	MGI			PMID:26046438
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0002409	decreased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223297
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0002410	decreased susceptibility to viral infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223297
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223297
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9223297
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669417
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669417
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0004209	abnormal sweet taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12581520
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0004210	abnormal bitter taste sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12581520
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0004867	decreased platelet calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669417
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669417
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20201022	MGI			
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0005586	decreased tidal volume		IEA		N	RGD:5509061	20260402	MGI			
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0009449	increased platelet ATP level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669417
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10669417
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0011678	abnormal vomeronasal sensory neuron physiology		IAGP		N	RGD:5509061	20160623	MGI			PMID:26046438
1557476	Plcb2	phospholipase C, beta 2	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20201002	MGI			PMID:10669417
1557478	Lcn10	lipocalin 10	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20241226	MGI			PMID:37392461
1557478	Lcn10	lipocalin 10	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20241226	MGI			PMID:37392461
1557478	Lcn10	lipocalin 10	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20241226	MGI			PMID:37392461
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210520	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0003063	increased coping response		IEA		N	RGD:5509061	20210826	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20210128	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20240523	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
1557479	Zzef1	zinc finger, ZZ-type with EF hand domain 1	gene	MP:0030610	absent teeth		IEA		N	RGD:5509061	20240523	MGI			
1557480	Lrrn1	leucine rich repeat protein 1, neuronal	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20141003	MGI			
1557480	Lrrn1	leucine rich repeat protein 1, neuronal	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20141003	MGI			
1557480	Lrrn1	leucine rich repeat protein 1, neuronal	gene	MP:0003169	abnormal scala media morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:37369584
1557480	Lrrn1	leucine rich repeat protein 1, neuronal	gene	MP:0004393	abnormal cochlear inner hair cell morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:37369584
1557480	Lrrn1	leucine rich repeat protein 1, neuronal	gene	MP:0004395	increased cochlear inner hair cell number		IAGP		N	RGD:5509061	20240229	MGI			PMID:37369584
1557481	Actrt3	actin related protein T3	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20260813	MGI			PMID:42391565
1557481	Actrt3	actin related protein T3	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20181227	MGI			
1557481	Actrt3	actin related protein T3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557481	Actrt3	actin related protein T3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20260813	MGI			PMID:42391565
1557481	Actrt3	actin related protein T3	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20260813	MGI			PMID:42391565
1557481	Actrt3	actin related protein T3	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:42391565
1557481	Actrt3	actin related protein T3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20260813	MGI			PMID:42391565
1557481	Actrt3	actin related protein T3	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20260813	MGI			PMID:42391565
1557481	Actrt3	actin related protein T3	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20231207	MGI			
1557481	Actrt3	actin related protein T3	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0030976	impaired sperm penetration of zona pellucida		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557481	Actrt3	actin related protein T3	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20260312	MGI			PMID:41668650
1557486	Osbpl3	oxysterol binding protein-like 3	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160114	MGI			
1557486	Osbpl3	oxysterol binding protein-like 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1557486	Osbpl3	oxysterol binding protein-like 3	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1557486	Osbpl3	oxysterol binding protein-like 3	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20241121	MGI			PMID:37740130
1557486	Osbpl3	oxysterol binding protein-like 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1557486	Osbpl3	oxysterol binding protein-like 3	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20200402	MGI			
1557486	Osbpl3	oxysterol binding protein-like 3	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20241121	MGI			PMID:37740130
1557486	Osbpl3	oxysterol binding protein-like 3	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20241121	MGI			PMID:37740130
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0000748	progressive muscle weakness		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20210826	MGI			
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0010014	hippocampus pyramidal cell degeneration		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557489	Gmppa	GDP-mannose pyrophosphorylase A	gene	MP:0020240	increased skeletal muscle cell apoptosis		IAGP		N	RGD:5509061	20210603	MGI			PMID:33755596
1557490	Mknk1	MAP kinase-interacting serine/threonine kinase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15254222
1557495	Hyal6	hyaluronoglucosaminidase 6	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1557495	Hyal6	hyaluronoglucosaminidase 6	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
1557495	Hyal6	hyaluronoglucosaminidase 6	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20241121	MGI			
1557496	Thsd7b	thrombospondin, type I, domain containing 7B	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1557496	Thsd7b	thrombospondin, type I, domain containing 7B	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20241121	MGI			
1557496	Thsd7b	thrombospondin, type I, domain containing 7B	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20250508	MGI			
1557496	Thsd7b	thrombospondin, type I, domain containing 7B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1557497	Megf11	multiple EGF-like-domains 11	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407321
1557497	Megf11	multiple EGF-like-domains 11	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407321
1557498	Stoml1	stomatin-like 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1557498	Stoml1	stomatin-like 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1557498	Stoml1	stomatin-like 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1557498	Stoml1	stomatin-like 1	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20220519	MGI			
1557498	Stoml1	stomatin-like 1	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20220519	MGI			
1557498	Stoml1	stomatin-like 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20220519	MGI			
1557498	Stoml1	stomatin-like 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20151001	MGI			PMID:24247984
1557498	Stoml1	stomatin-like 1	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20210128	MGI			
1557498	Stoml1	stomatin-like 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20210128	MGI			
1557500	H1f8	H1.8 linker histone	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557500	H1f8	H1.8 linker histone	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1557500	H1f8	H1.8 linker histone	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1557500	H1f8	H1.8 linker histone	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0000523	cortical renal glomerulopathies		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20210121	MGI			PMID:32876667
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0001566	increased circulating phosphate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210121	MGI			PMID:32876667
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002269	muscular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002828	abnormal renal glomerular capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0002966	decreased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0003793	abnormal submandibular gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20210121	MGI			PMID:32876667
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0009417	skeletal muscle atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011348	abnormal renal glomerulus basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011352	proximal convoluted tubule brush border loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011359	decreased glomerular capillary number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12858174
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011377	renal glomerulus fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011453	abnormal glomerular capillary endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011454	abnormal glomerular endothelium fenestra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011498	abnormal glomerular capsule parietal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557502	Rrm2b	ribonucleotide reductase M2 B (TP53 inducible)	gene	MP:0011871	podocyte hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15723268
1557504	Lrrcc1	leucine rich repeat and coiled-coil domain containing 1	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20210805	MGI			
1557504	Lrrcc1	leucine rich repeat and coiled-coil domain containing 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1557504	Lrrcc1	leucine rich repeat and coiled-coil domain containing 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20210805	MGI			
1557504	Lrrcc1	leucine rich repeat and coiled-coil domain containing 1	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1557505	Atoh8	atonal bHLH transcription factor 8	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18560595
1557505	Atoh8	atonal bHLH transcription factor 8	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23836893
1557506	Washc5	WASH complex subunit 5	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1557506	Washc5	WASH complex subunit 5	gene	MP:0002877	abnormal melanocyte morphology		IAGP		N	RGD:5509061	20171116	MGI			PMID:27390154
1557506	Washc5	WASH complex subunit 5	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1557506	Washc5	WASH complex subunit 5	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20181129	MGI			PMID:26572744
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:29950491
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20190418	MGI			PMID:29950491
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0000536	hydroureter		IAGP		N	RGD:5509061	20190418	MGI			PMID:29950491
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0000539	distended urinary bladder		IAGP		N	RGD:5509061	20190418	MGI			PMID:29950491
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20230803	MGI			PMID:36727488
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20220811	MGI			
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20221215	MGI			
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20221215	MGI			
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20230803	MGI			PMID:36727488
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20190418	MGI			PMID:29950491
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20221215	MGI			
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20190418	MGI			PMID:29950491
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20190418	MGI			PMID:29950491
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20230803	MGI			PMID:36727488
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190418	MGI			PMID:29950491
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1557512	Dis3l2	DIS3 like 3'-5' exoribonuclease 2	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20230803	MGI			PMID:36727488
1557514	Zmym6	zinc finger, MYM-type 6	gene	MP:0000280	thin ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
1557515	Plekha8	pleckstrin homology domain containing A8	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1557515	Plekha8	pleckstrin homology domain containing A8	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20170105	MGI			
1557515	Plekha8	pleckstrin homology domain containing A8	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20170105	MGI			
1557515	Plekha8	pleckstrin homology domain containing A8	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20210128	MGI			
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20231207	MGI			
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557516	Tbc1d25	TBC1 domain family, member 25	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20201105	MGI			PMID:32210723
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20181227	MGI			
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20190228	MGI			PMID:29905857
1557517	Gfpt1	glutamine fructose-6-phosphate transaminase 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557519	Tfe3	transcription factor E3	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1557519	Tfe3	transcription factor E3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1557519	Tfe3	transcription factor E3	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1557519	Tfe3	transcription factor E3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1557519	Tfe3	transcription factor E3	gene	MP:0003053	delayed tooth eruption		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1557519	Tfe3	transcription factor E3	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1557519	Tfe3	transcription factor E3	gene	MP:0005171	absent coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1557519	Tfe3	transcription factor E3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1557519	Tfe3	transcription factor E3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11930005
1557520	Aldh16a1	aldehyde dehydrogenase 16 family, member A1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1557520	Aldh16a1	aldehyde dehydrogenase 16 family, member A1	gene	MP:0001765	abnormal ion homeostasis		IAGP		N	RGD:5509061	20190221	MGI			PMID:28254523
1557520	Aldh16a1	aldehyde dehydrogenase 16 family, member A1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20190221	MGI			PMID:28254523
1557520	Aldh16a1	aldehyde dehydrogenase 16 family, member A1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20141003	MGI			
1557520	Aldh16a1	aldehyde dehydrogenase 16 family, member A1	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20250508	MGI			
1557521	Ifi204	interferon activated gene 204	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1557521	Ifi204	interferon activated gene 204	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20190912	MGI			PMID:29472103
1557521	Ifi204	interferon activated gene 204	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20190912	MGI			PMID:29472103
1557521	Ifi204	interferon activated gene 204	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20190912	MGI			PMID:29472103
1557521	Ifi204	interferon activated gene 204	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20190912	MGI			PMID:29472103
1557521	Ifi204	interferon activated gene 204	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20190912	MGI			PMID:29472103
1557521	Ifi204	interferon activated gene 204	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20190912	MGI			PMID:29472103
1557521	Ifi204	interferon activated gene 204	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20190912	MGI			PMID:29472103
1557521	Ifi204	interferon activated gene 204	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20190912	MGI			PMID:29472103
1557522	Ccny	cyclin Y	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0005334	abnormal fat pad morphology		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0009303	decreased renal fat pad weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0009305	decreased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0010378	increased respiratory quotient		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20151008	MGI			PMID:26305884
1557522	Ccny	cyclin Y	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557522	Ccny	cyclin Y	gene	MP:0011698	abnormal brown adipose tissue physiology		IAGP		N	RGD:5509061	20151008	MGI			PMID:26161966
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20160331	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20160331	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200220	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20200220	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20160331	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20231207	MGI			
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21285371
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20160331	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20200220	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20200220	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20160331	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0002969	impaired social transmission of food preference		IAGP		N	RGD:5509061	20160331	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20231207	MGI			
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20200220	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20160331	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0005237	abnormal olfactory tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0005267	abnormal olfactory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20231207	MGI			
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20231207	MGI			
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20231207	MGI			
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20160331	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0009941	abnormal olfactory bulb interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0009947	abnormal olfactory bulb external plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0009951	abnormal olfactory bulb mitral cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0009954	abnormal mitral cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0009955	abnormal olfactory bulb tufted cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0010059	olfactory bulb hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9883721
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200220	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0011620	abnormal habituation to a new environment		IAGP		N	RGD:5509061	20200220	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0014115	cognitive inflexibility		IAGP		N	RGD:5509061	20160331	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0014382	increased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20161013	MGI			PMID:24441682
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0020870	decreased thigmotaxis		IAGP		N	RGD:5509061	20200220	MGI			PMID:31680851
1557526	Tbr1	T-box brain transcription factor 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:31680851
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0008440	abnormal subplate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0008442	disorganized cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557530	Brsk1	BR serine/threonine kinase 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15705853
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220519	MGI			
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20220519	MGI			
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220811	MGI			PMID:34096614
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220811	MGI			PMID:34096614
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20220519	MGI			
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:34096614
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:34096614
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:34096614
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0003883	enlarged stomach		IEA		N	RGD:5509061	20220519	MGI			
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:34096614
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:34096614
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0014631	abnormal elongated spermatid morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20190207	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0031373	abnormal manchette perinuclear ring morphology		IAGP		N	RGD:5509061	20220407	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0031375	abnormal manchette disassembly		IAGP		N	RGD:5509061	20220407	MGI			PMID:29136647
1557532	Katnal2	katanin p60 subunit A-like 2	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20220428	MGI			PMID:29136647
1557534	Cdx4	caudal type homeobox 4	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0003445	sirenomelia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0012127	absent placenta hemotrichorial membrane		IAGP		N	RGD:5509061	20141003	MGI			PMID:16396910
1557534	Cdx4	caudal type homeobox 4	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:18511567
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020030
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19625617
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020030
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020030
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0001746	abnormal pituitary secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19625617
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0003506	acromegaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0003838	abnormal milk ejection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020030
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020030
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020030
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0008028	pregnancy-related premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020030
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:19625617
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0008779	abnormal maternal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19625617
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19625617
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19020030
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19625617
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19625617
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0012010	parturition failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240328	MGI			PMID:19625617
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0014379	decreased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:19020030
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0014920	increased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0030567	abnormal I band morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:23116210
1557535	Kalrn	kalirin, RhoGEF kinase	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:19625617
1557537	Med12	mediator complex subunit 12	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589884
1557537	Med12	mediator complex subunit 12	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589884
1557537	Med12	mediator complex subunit 12	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0001691	abnormal somite shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589884
1557537	Med12	mediator complex subunit 12	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0002950	abnormal neural crest cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589884
1557537	Med12	mediator complex subunit 12	gene	MP:0003400	kinked neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0004601	abnormal vertebral spinous process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589884
1557537	Med12	mediator complex subunit 12	gene	MP:0004603	absent vertebral arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589884
1557537	Med12	mediator complex subunit 12	gene	MP:0005223	abnormal dorsal-ventral polarity of the somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0006345	absent second pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589884
1557537	Med12	mediator complex subunit 12	gene	MP:0010642	absent third pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589884
1557537	Med12	mediator complex subunit 12	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20589884
1557537	Med12	mediator complex subunit 12	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0011732	decreased somite size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557537	Med12	mediator complex subunit 12	gene	MP:0012159	absent anterior visceral endoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:20630950
1557538	Lipn	lipase family member N	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1557539	Casz1	castor zinc finger 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20221215	MGI			
1557539	Casz1	castor zinc finger 1	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20250508	MGI			
1557539	Casz1	castor zinc finger 1	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0004062	dilated heart right atrium		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0008727	increased heart right atrium size		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0010019	liver vascular congestion		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0010200	enlarged lymphatic vessel		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0010422	heart right ventricle hypoplasia		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0010500	myocardium hypoplasia		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0010640	ventricular myocardium compact layer hypoplasia		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557539	Casz1	castor zinc finger 1	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0012269	nuchal edema		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0012515	abnormal heart apex morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20170803	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0031511	globular heart		IAGP		N	RGD:5509061	20231102	MGI			PMID:25190801
1557539	Casz1	castor zinc finger 1	gene	MP:0031611	decreased fetal cardiomyocyte number		IAGP		N	RGD:5509061	20240321	MGI			PMID:25953344
1557539	Casz1	castor zinc finger 1	gene	MP:0031613	fetal cardiomyocyte disarray		IAGP		N	RGD:5509061	20240321	MGI			PMID:25190801
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0002812	spherocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0008807	increased liver iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0008808	decreased spleen iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0008956	decreased cellular hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9927493
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557540	Epb41	erythrocyte membrane protein band 4.1	gene	MP:0014990	enhanced erythropoiesis		IAGP		N	RGD:5509061	20260507	MGI			PMID:9927493
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0012119	increased trophectoderm apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22984479
1557542	Usp17lc	ubiquitin specific peptidase 17-like C	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:22984479
1557544	Nod1	nucleotide-binding oligomerization domain containing 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16418393
1557544	Nod1	nucleotide-binding oligomerization domain containing 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1557544	Nod1	nucleotide-binding oligomerization domain containing 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16418393
1557544	Nod1	nucleotide-binding oligomerization domain containing 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1557544	Nod1	nucleotide-binding oligomerization domain containing 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16418393
1557544	Nod1	nucleotide-binding oligomerization domain containing 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1557544	Nod1	nucleotide-binding oligomerization domain containing 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18261938
1557544	Nod1	nucleotide-binding oligomerization domain containing 1	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16418393
1557546	Lats1	large tumor suppressor	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20150910	MGI			PMID:26109051
1557546	Lats1	large tumor suppressor	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230145
1557546	Lats1	large tumor suppressor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1557546	Lats1	large tumor suppressor	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230145
1557546	Lats1	large tumor suppressor	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1557546	Lats1	large tumor suppressor	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1557546	Lats1	large tumor suppressor	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1557546	Lats1	large tumor suppressor	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20150910	MGI			PMID:26109051
1557546	Lats1	large tumor suppressor	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230145
1557546	Lats1	large tumor suppressor	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230145
1557546	Lats1	large tumor suppressor	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230145
1557546	Lats1	large tumor suppressor	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0009009	absent estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1557546	Lats1	large tumor suppressor	gene	MP:0009733	absent nipple		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230145
1557546	Lats1	large tumor suppressor	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557546	Lats1	large tumor suppressor	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200514	MGI			
1557546	Lats1	large tumor suppressor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230145
1557546	Lats1	large tumor suppressor	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230145
1557546	Lats1	large tumor suppressor	gene	MP:0013348	adenohypophysis hyperplasia		IAGP		N	RGD:5509061	20150129	MGI			PMID:9988269
1557546	Lats1	large tumor suppressor	gene	MP:0013611	abnormal bile duct epithelium morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:26109051
1557546	Lats1	large tumor suppressor	gene	MP:0030943	abnormal centrosome morphology		IAGP		N	RGD:5509061	20190718	MGI			PMID:23230145
1557547	Gnpnat1	glucosamine-phosphate N-acetyltransferase 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013212
1557547	Gnpnat1	glucosamine-phosphate N-acetyltransferase 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013212
1557547	Gnpnat1	glucosamine-phosphate N-acetyltransferase 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013212
1557547	Gnpnat1	glucosamine-phosphate N-acetyltransferase 1	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013212
1557547	Gnpnat1	glucosamine-phosphate N-acetyltransferase 1	gene	MP:0003087	absent allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013212
1557547	Gnpnat1	glucosamine-phosphate N-acetyltransferase 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013212
1557547	Gnpnat1	glucosamine-phosphate N-acetyltransferase 1	gene	MP:0005030	absent amnion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013212
1557547	Gnpnat1	glucosamine-phosphate N-acetyltransferase 1	gene	MP:0009593	absent chorion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013212
1557547	Gnpnat1	glucosamine-phosphate N-acetyltransferase 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013212
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20191003	MGI			PMID:31147515
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0003279	aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:31147515
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20191003	MGI			PMID:31147515
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:31147515
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0006278	aortic aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0006355	abnormal sixth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0009868	abnormal descending thoracic aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0010425	abnormal heart and great vessel attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0010652	absent aorticopulmonary septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0010666	abnormal vitelline vein morphology		IAGP		N	RGD:5509061	20150521	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204380
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17183527
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0011707	impaired fibroblast cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:20534669
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0012729	abnormal common carotid artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0012751	impaired cardiac neural crest cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15951419
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0013187	dilated basilar artery		IAGP		N	RGD:5509061	20141003	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:22899851
1557548	Mrtfb	myocardin related transcription factor B	gene	MP:0030338	dilated third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:22899851
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20240523	MGI			
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0004911	absent mandibular condyloid process		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221020	MGI			PMID:34732852
1557549	Zfhx4	zinc finger homeodomain 4	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:34732852
1557550	Tbx15	T-box 15	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0000023	abnormal ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0000024	lowered ear position		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20171214	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0000167	decreased chondrocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:13654621
1557550	Tbx15	T-box 15	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:13654621
1557550	Tbx15	T-box 15	gene	MP:0000435	shortened head		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0000449	broad nasal bridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:13654621
1557550	Tbx15	T-box 15	gene	MP:0000449	broad nasal bridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0001300	ocular hypertelorism		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:13654621
1557550	Tbx15	T-box 15	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:13654621
1557550	Tbx15	T-box 15	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13654621
1557550	Tbx15	T-box 15	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0003419	delayed endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004338	small clavicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004339	absent clavicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004342	scapular bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:13654621
1557550	Tbx15	T-box 15	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004343	small scapula		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0004345	abnormal acromion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004347	abnormal scapular spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004353	abnormal deltoid tuberosity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004447	small basioccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004508	abnormal pectoral girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0004599	abnormal vertebral arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004659	abnormal odontoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0004659	abnormal odontoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141225	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0008154	decreased diameter of humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0008237	abnormal ventral coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0008238	abnormal dorsoventral coat patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14737183
1557550	Tbx15	T-box 15	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0008526	decreased cranium width		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728667
1557550	Tbx15	T-box 15	gene	MP:0010941	abnormal foramen magnum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:13654621
1557550	Tbx15	T-box 15	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0030833	small acromion		IAGP		N	RGD:5509061	20181018	MGI			PMID:13654621
1557550	Tbx15	T-box 15	gene	MP:0030833	small acromion		IAGP		N	RGD:5509061	20181018	MGI			PMID:15652702
1557550	Tbx15	T-box 15	gene	MP:0030833	small acromion		IAGP		N	RGD:5509061	20181018	MGI			PMID:15728667
1557551	Cyth4	cytohesin 4	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20240523	MGI			
1557551	Cyth4	cytohesin 4	gene	MP:0005573	increased pulmonary respiratory rate		IEA		N	RGD:5509061	20241121	MGI			
1557551	Cyth4	cytohesin 4	gene	MP:0006415	absent testes		IEA		N	RGD:5509061	20240523	MGI			
1557551	Cyth4	cytohesin 4	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20240523	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000061	fragile skeleton		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20150827	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000642	enlarged adrenal glands		IEA		N	RGD:5509061	20150827	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20241121	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242664
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001548	hyperlipidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20150827	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242664
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11280729
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789047
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10757812
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0002925	abnormal cardiovascular development		IEA		N	RGD:5509061	20150827	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0003789	increased osteosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0003820	increased left ventricle systolic pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12242664
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20241121	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10757812
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0009304	increased retroperitoneal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:11280729
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0010484	bicuspid aortic valve		IEA		N	RGD:5509061	20150827	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0010527	bicuspid pulmonary valve		IEA		N	RGD:5509061	20150827	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0010867	abnormal bone trabecula morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0010873	decreased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15235603
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0010924	abnormal osteoid morphology		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789047
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20151126	MGI			PMID:24626990
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0014427	increased circulating hyaluronic acid level		IAGP		N	RGD:5509061	20240425	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170202	MGI			PMID:16330174
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20241121	MGI			
1557552	Wrn	Werner syndrome RecQ like helicase	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:15235603
1557555	Cntrl	centriolin	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20141003	MGI			
1557555	Cntrl	centriolin	gene	MP:0000519	hydronephrosis		IEA		N	RGD:5509061	20141003	MGI			
1557555	Cntrl	centriolin	gene	MP:0000536	hydroureter		IEA		N	RGD:5509061	20151203	MGI			
1557555	Cntrl	centriolin	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20151203	MGI			
1557555	Cntrl	centriolin	gene	MP:0003675	kidney cyst		IEA		N	RGD:5509061	20141003	MGI			
1557555	Cntrl	centriolin	gene	MP:0004200	decreased fetal size		IEA		N	RGD:5509061	20151203	MGI			
1557555	Cntrl	centriolin	gene	MP:0004860	dilated kidney collecting duct		IEA		N	RGD:5509061	20151203	MGI			
1557555	Cntrl	centriolin	gene	MP:0006124	tricuspid valve stenosis		IEA		N	RGD:5509061	20141003	MGI			
1557555	Cntrl	centriolin	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20151203	MGI			
1557555	Cntrl	centriolin	gene	MP:0010402	ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1557555	Cntrl	centriolin	gene	MP:0010403	atrial septal defect		IEA		N	RGD:5509061	20141003	MGI			
1557555	Cntrl	centriolin	gene	MP:0010422	heart right ventricle hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1557555	Cntrl	centriolin	gene	MP:0010457	pulmonary artery stenosis		IEA		N	RGD:5509061	20151203	MGI			
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0000578	ulcerated autopod		IAGP		N	RGD:5509061	20141003	MGI			PMID:18806225
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22649252
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21239721
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855887
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002297	abnormal forced expiratory flow rates		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21760953
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12935356
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322195
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312165
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855817
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872135
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21760953
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855817
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855817
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16714379
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855887
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0003691	abnormal microglial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22649252
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17190817
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312165
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17190817
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:18423196
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22796522
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20505141
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981228
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21760953
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21760953
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855887
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008552	abnormal circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18713975
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12935356
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008554	decreased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312165
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008557	abnormal interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998457
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872135
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550345
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18423196
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18178804
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855887
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312165
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21239721
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21760953
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312165
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855817
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872135
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855887
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12855817
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802464
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0010750	increased susceptibility to parasitic infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21760953
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0011077	decreased macrophage nitric oxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872135
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0011077	decreased macrophage nitric oxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872135
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082622
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312165
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0011081	decreased macrophage apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12872135
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0011081	decreased macrophage apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15322195
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0013022	increased Ly6C high monocyte number		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0013026	decreased Ly6C low monocyte number		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20150219	MGI			PMID:24557836
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:12872135
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0020927	abnormal susceptibility to Poxviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18802464
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:21239721
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:21998457
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0020947	decreased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18423196
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0031040	increased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:21239721
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0031040	increased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:21998457
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0031048	increased susceptibility to Coronaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200625	MGI			PMID:26015500
1557557	Ticam1	TIR domain containing adaptor molecule 1	gene	MP:0031266	decreased susceptibility to alcohol-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:18713975
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20171207	MGI			PMID:28263186
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20171207	MGI			PMID:28263186
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0004230	abnormal embryonic erythrocyte morphology		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0005650	abnormal limb bud morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:28263186
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0011261	abnormal limb mesenchyme morphology		IAGP		N	RGD:5509061	20171207	MGI			PMID:28263186
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20170601	MGI			PMID:26544067
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20171207	MGI			PMID:28263186
1557559	Ddrgk1	DDRGK domain containing 1	gene	MP:0031750	impaired embryonic erythropoiesis		IAGP		N	RGD:5509061	20260709	MGI			PMID:26544067
1557562	Tbx3	T-box 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22130515
1557562	Tbx3	T-box 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460765
1557562	Tbx3	T-box 3	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22130515
1557562	Tbx3	T-box 3	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0000555	absent carpal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0000555	absent carpal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473172
1557562	Tbx3	T-box 3	gene	MP:0000629	absent mammary gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0001142	abnormal vagina orifice morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460765
1557562	Tbx3	T-box 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230119	MGI			
1557562	Tbx3	T-box 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20260402	MGI			
1557562	Tbx3	T-box 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1557562	Tbx3	T-box 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1557562	Tbx3	T-box 3	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0001679	thin apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460765
1557562	Tbx3	T-box 3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1557562	Tbx3	T-box 3	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473172
1557562	Tbx3	T-box 3	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19769959
1557562	Tbx3	T-box 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230119	MGI			
1557562	Tbx3	T-box 3	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20260402	MGI			
1557562	Tbx3	T-box 3	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20231207	MGI			
1557562	Tbx3	T-box 3	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1557562	Tbx3	T-box 3	gene	MP:0003074	absent metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0003127	abnormal clitoris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0003137	abnormal impulse conducting system conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460765
1557562	Tbx3	T-box 3	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0003898	abnormal QRS complex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0003928	increased heart rate variability		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22130515
1557562	Tbx3	T-box 3	gene	MP:0004070	abnormal P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0004115	abnormal sinoatrial node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473172
1557562	Tbx3	T-box 3	gene	MP:0004122	abnormal sinus arrhythmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0004135	abnormal mammary gland embryonic development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460765
1557562	Tbx3	T-box 3	gene	MP:0004360	absent ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0004576	abnormal embryonic autopod plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0006107	abnormal fetal atrioventricular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460765
1557562	Tbx3	T-box 3	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20231207	MGI			
1557562	Tbx3	T-box 3	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0009328	delayed heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:17460765
1557562	Tbx3	T-box 3	gene	MP:0009382	abnormal cardiac jelly morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22130515
1557562	Tbx3	T-box 3	gene	MP:0009729	absent tarsus bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:19769959
1557562	Tbx3	T-box 3	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19769959
1557562	Tbx3	T-box 3	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1557562	Tbx3	T-box 3	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0010510	absent P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0010511	shortened PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0010512	absent PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0010637	sinus bradycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17473172
1557562	Tbx3	T-box 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19769959
1557562	Tbx3	T-box 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19769959
1557562	Tbx3	T-box 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0013169	small hindlimb buds		IAGP		N	RGD:5509061	20141003	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1557562	Tbx3	T-box 3	gene	MP:0013785	abnormal mammary gland bud morphology		IAGP		N	RGD:5509061	20150611	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:17460765
1557562	Tbx3	T-box 3	gene	MP:0020515	abnormal visceral yolk sac endoderm morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:12668638
1557562	Tbx3	T-box 3	gene	MP:0031541	decreased sinoatrial node size		IAGP		N	RGD:5509061	20240104	MGI			PMID:17473172
1557562	Tbx3	T-box 3	gene	MP:0031542	sinoatrial node hypoplasia		IAGP		N	RGD:5509061	20240104	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0031728	atrial arrhythmia		IAGP		N	RGD:5509061	20260618	MGI			PMID:22203979
1557562	Tbx3	T-box 3	gene	MP:0031757	second degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:22203979
1557563	Nup42	nucleoporin 42	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1557563	Nup42	nucleoporin 42	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20260402	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0000272	abnormal aorta morphology		IEA		N	RGD:5509061	20141003	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20141003	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636176
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0001299	abnormal eye distance/ position		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20181227	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0002746	abnormal semilunar valve morphology		IEA		N	RGD:5509061	20141003	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0002748	abnormal pulmonary valve morphology		IEA		N	RGD:5509061	20141003	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0004383	absent interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0006301	abnormal mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9636176
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0010418	perimembraneous ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0010469	ascending aorta hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0010476	coronary fistula		IEA		N	RGD:5509061	20141003	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0010541	aorta hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0030028	absent exoccipital bone		IAGP		N	RGD:5509061	20170810	MGI			PMID:17442300
1557564	Hectd1	HECT domain E3 ubiquitin protein ligase 1	gene	MP:0030329	absent temporal bone petrous part		IAGP		N	RGD:5509061	20171109	MGI			PMID:17442300
1557565	Arhgef38	Rho guanine nucleotide exchange factor 38	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20181227	MGI			
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20201022	MGI			
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0001128	ovary hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20181227	MGI			
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20201022	MGI			
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921895
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10921895
1557567	Tial1	Tia1 cytotoxic granule-associated RNA binding protein-like 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9482885
1557569	Pax7	paired box 7	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631261
1557569	Pax7	paired box 7	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410975
1557569	Pax7	paired box 7	gene	MP:0000448	pointed snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631261
1557569	Pax7	paired box 7	gene	MP:0000457	maxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631261
1557569	Pax7	paired box 7	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19554048
1557569	Pax7	paired box 7	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1557569	Pax7	paired box 7	gene	MP:0000734	muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0000737	abnormal myotome development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843801
1557569	Pax7	paired box 7	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11030621
1557569	Pax7	paired box 7	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11030621
1557569	Pax7	paired box 7	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282552
1557569	Pax7	paired box 7	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19554048
1557569	Pax7	paired box 7	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828093
1557569	Pax7	paired box 7	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945933
1557569	Pax7	paired box 7	gene	MP:0000750	abnormal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410975
1557569	Pax7	paired box 7	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:38829202
1557569	Pax7	paired box 7	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11030621
1557569	Pax7	paired box 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
1557569	Pax7	paired box 7	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213072
1557569	Pax7	paired box 7	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20241212	MGI			PMID:38829202
1557569	Pax7	paired box 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11030621
1557569	Pax7	paired box 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631261
1557569	Pax7	paired box 7	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239359
1557569	Pax7	paired box 7	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24239359
1557569	Pax7	paired box 7	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20170420	MGI			PMID:26987019
1557569	Pax7	paired box 7	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20170420	MGI			PMID:26987019
1557569	Pax7	paired box 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828093
1557569	Pax7	paired box 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631261
1557569	Pax7	paired box 7	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945933
1557569	Pax7	paired box 7	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1557569	Pax7	paired box 7	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19332644
1557569	Pax7	paired box 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180322	MGI			PMID:29415061
1557569	Pax7	paired box 7	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1557569	Pax7	paired box 7	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20241212	MGI			PMID:38829202
1557569	Pax7	paired box 7	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282552
1557569	Pax7	paired box 7	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828091
1557569	Pax7	paired box 7	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828093
1557569	Pax7	paired box 7	gene	MP:0003833	decreased satellite cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:38829202
1557569	Pax7	paired box 7	gene	MP:0004477	turbinate hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828093
1557569	Pax7	paired box 7	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631261
1557569	Pax7	paired box 7	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828093
1557569	Pax7	paired box 7	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
1557569	Pax7	paired box 7	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1557569	Pax7	paired box 7	gene	MP:0005247	abnormal extraocular muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19531352
1557569	Pax7	paired box 7	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20211209	MGI			PMID:33753492
1557569	Pax7	paired box 7	gene	MP:0006039	decreased mitochondrial fission		IAGP		N	RGD:5509061	20211209	MGI			PMID:33753492
1557569	Pax7	paired box 7	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19213072
1557569	Pax7	paired box 7	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1557569	Pax7	paired box 7	gene	MP:0008052	abnormal serous gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631261
1557569	Pax7	paired box 7	gene	MP:0009398	abnormal skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
1557569	Pax7	paired box 7	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:11030621
1557569	Pax7	paired box 7	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0009402	decreased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0009407	increased skeletal muscle fiber density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0009410	abnormal skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19554048
1557569	Pax7	paired box 7	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828091
1557569	Pax7	paired box 7	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22945933
1557569	Pax7	paired box 7	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828093
1557569	Pax7	paired box 7	gene	MP:0010238	increased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
1557569	Pax7	paired box 7	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
1557569	Pax7	paired box 7	gene	MP:0010240	decreased skeletal muscle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20241212	MGI			PMID:38829202
1557569	Pax7	paired box 7	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20211209	MGI			PMID:33753492
1557569	Pax7	paired box 7	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20211209	MGI			PMID:33753492
1557569	Pax7	paired box 7	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20211209	MGI			PMID:33753492
1557569	Pax7	paired box 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869749
1557569	Pax7	paired box 7	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8631261
1557569	Pax7	paired box 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20241212	MGI			PMID:38829202
1557569	Pax7	paired box 7	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843801
1557569	Pax7	paired box 7	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20211209	MGI			PMID:33753492
1557569	Pax7	paired box 7	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17418413
1557569	Pax7	paired box 7	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23410975
1557569	Pax7	paired box 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557569	Pax7	paired box 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557569	Pax7	paired box 7	gene	MP:0011808	abnormal myoblast differentiation		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1557569	Pax7	paired box 7	gene	MP:0012185	abnormal muscle precursor cell morphology		IAGP		N	RGD:5509061	20160721	MGI			PMID:26999603
1557569	Pax7	paired box 7	gene	MP:0012185	abnormal muscle precursor cell morphology		IAGP		N	RGD:5509061	20210513	MGI			PMID:32094117
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22279050
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23933088
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20160721	MGI			PMID:26999603
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20190704	MGI			PMID:26854227
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20201217	MGI			PMID:31685980
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:19554048
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:21828091
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:21828093
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211209	MGI			PMID:33753492
1557569	Pax7	paired box 7	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20241212	MGI			PMID:38829202
1557569	Pax7	paired box 7	gene	MP:0014921	decreased sarcomere length		IAGP		N	RGD:5509061	20260219	MGI			PMID:38829202
1557569	Pax7	paired box 7	gene	MP:0030056	lacrimal bone hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:15520281
1557569	Pax7	paired box 7	gene	MP:0031328	delayed skeletal muscle regeneration		IAGP		N	RGD:5509061	20220106	MGI			PMID:32483152
1557571	Slc39a1	solute carrier family 39 (zinc transporter), member 1	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1557571	Slc39a1	solute carrier family 39 (zinc transporter), member 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1557571	Slc39a1	solute carrier family 39 (zinc transporter), member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151203	MGI			PMID:16652366
1557571	Slc39a1	solute carrier family 39 (zinc transporter), member 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1557571	Slc39a1	solute carrier family 39 (zinc transporter), member 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1557571	Slc39a1	solute carrier family 39 (zinc transporter), member 1	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16652366
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11454988
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0001556	increased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8706124
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594290
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594290
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213735
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770692
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0003666	impaired sperm capacitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213735
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594290
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7600574
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213735
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12213735
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770692
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770692
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23770692
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0012507	midbrain atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20161013	MGI			PMID:7670466
1557572	Smpd1	sphingomyelin phosphodiesterase 1, acid lysosomal	gene	MP:0031058	hepatosplenomegaly		IAGP		N	RGD:5509061	20200618	MGI			PMID:7600574
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0004121	abnormal sarcolemma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0009415	skeletal muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0010011	ectopic hippocampus pyramidal cells		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23630012
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0011150	abnormal hippocampus stratum oriens morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557573	Pik3r4	phosphoinositide-3-kinase regulatory subunit 4	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12860565
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12860565
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007846
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18438411
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18438411
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12860565
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12626533
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9625767
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918981
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:18438411
1557574	Irak1	interleukin-1 receptor-associated kinase 1	gene	MP:0010087	increased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1557578	Trex2	three prime repair exonuclease 2	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19654293
1557578	Trex2	three prime repair exonuclease 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19654293
1557578	Trex2	three prime repair exonuclease 2	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19654293
1557578	Trex2	three prime repair exonuclease 2	gene	MP:0009581	decreased keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19654293
1557579	Fgfbp3	fibroblast growth factor binding protein 3	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1557579	Fgfbp3	fibroblast growth factor binding protein 3	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20851768
1557581	Krt18	keratin 18	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9508776
1557581	Krt18	keratin 18	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0001656	focal hepatic necrosis		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013209
1557581	Krt18	keratin 18	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013209
1557581	Krt18	keratin 18	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013209
1557581	Krt18	keratin 18	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013209
1557581	Krt18	keratin 18	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557581	Krt18	keratin 18	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11013209
1557581	Krt18	keratin 18	gene	MP:0014045	Mallory bodies		IAGP		N	RGD:5509061	20220609	MGI			PMID:27689336
1557582	Tatdn3	TatD DNase domain containing 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20170105	MGI			
1557582	Tatdn3	TatD DNase domain containing 3	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1557582	Tatdn3	TatD DNase domain containing 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1557584	Tbx22	T-box 22	gene	MP:0000098	abnormal vomer bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1557584	Tbx22	T-box 22	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1557584	Tbx22	T-box 22	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1557584	Tbx22	T-box 22	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0008970	choanal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0009892	palate bone hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0013264	tongue ankylosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0030183	persistent oronasal membrane		IAGP		N	RGD:5509061	20171012	MGI			PMID:19648291
1557584	Tbx22	T-box 22	gene	MP:0030266	small vomer bone		IAGP		N	RGD:5509061	20171026	MGI			PMID:19648291
1557585	Cad	carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20191128	MGI			PMID:29551634
1557585	Cad	carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201022	MGI			
1557585	Cad	carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20191128	MGI			PMID:29551634
1557585	Cad	carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1557585	Cad	carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557585	Cad	carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1557586	Naaa	N-acylethanolamine acid amidase	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1557586	Naaa	N-acylethanolamine acid amidase	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1557586	Naaa	N-acylethanolamine acid amidase	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1557586	Naaa	N-acylethanolamine acid amidase	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20250116	MGI			PMID:29054595
1557586	Naaa	N-acylethanolamine acid amidase	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1557586	Naaa	N-acylethanolamine acid amidase	gene	MP:0010073	decreased pruritus		IAGP		N	RGD:5509061	20250116	MGI			PMID:29054595
1557588	Tenm1	teneurin transmembrane protein 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20230119	MGI			
1557588	Tenm1	teneurin transmembrane protein 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230119	MGI			
1557588	Tenm1	teneurin transmembrane protein 1	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230119	MGI			
1557588	Tenm1	teneurin transmembrane protein 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20230119	MGI			
1557588	Tenm1	teneurin transmembrane protein 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20250508	MGI			
1557588	Tenm1	teneurin transmembrane protein 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230119	MGI			
1557588	Tenm1	teneurin transmembrane protein 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20230119	MGI			
1557588	Tenm1	teneurin transmembrane protein 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20250508	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0000116	abnormal tooth development		IEA		N	RGD:5509061	20120209	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0000119	abnormal tooth eruption		IEA		N	RGD:5509061	20111116	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:5959976
1557590	Eda	ectodysplasin-A	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20250508	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20250508	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0000372	irregular coat pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0000396	increased curvature of hairs		IEA		N	RGD:5509061	20111116	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0000397	abnormal guard hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2348861
1557590	Eda	ectodysplasin-A	gene	MP:0000577	absent eccrine glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0000577	absent eccrine glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:2348861
1557590	Eda	ectodysplasin-A	gene	MP:0000577	absent eccrine glands		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0000675	abnormal eccrine sweat gland morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20181101	MGI			PMID:7544943
1557590	Eda	ectodysplasin-A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0001284	absent vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0001302	eyelids open at birth		IEA		N	RGD:5509061	20120209	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20141003	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20250508	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932191
1557590	Eda	ectodysplasin-A	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20170314	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0002163	abnormal gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0002277	abnormal respiratory mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973734
1557590	Eda	ectodysplasin-A	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0002717	abnormal male preputial gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0002789	male pseudohermaphroditism		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0002832	coarse hair		IEA		N	RGD:5509061	20111116	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20181101	MGI			PMID:7544943
1557590	Eda	ectodysplasin-A	gene	MP:0003815	hairless		IEA		N	RGD:5509061	20120209	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:478295
1557590	Eda	ectodysplasin-A	gene	MP:0004381	abnormal hair follicle melanocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0004830	short incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:5959976
1557590	Eda	ectodysplasin-A	gene	MP:0005176	eyelids fail to open		IEA		N	RGD:5509061	20120209	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5959976
1557590	Eda	ectodysplasin-A	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0006236	absent Meibomian glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0006236	absent Meibomian glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0006236	absent Meibomian glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0006363	absent auchene hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0006366	absent zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0006366	absent zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0006366	absent zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0006366	absent zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0006367	absent sweat gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0006369	supernumerary incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0006370	abnormal hair follicle pheomelanosome pheomelanin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0006371	absent hair follicle pheomelanosome pheomelanin		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5959976
1557590	Eda	ectodysplasin-A	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0006401	absent male preputial gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:478295
1557590	Eda	ectodysplasin-A	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:5959976
1557590	Eda	ectodysplasin-A	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0008538	decreased zigzag hair amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0009003	abnormal vibrissa number		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0009652	abnormal palatal rugae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18028050
1557590	Eda	ectodysplasin-A	gene	MP:0009659	striated fur		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0009659	striated fur		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0009793	sebaceous gland hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0009794	sebaceous gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0010031	abnormal cranium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0010231	transverse fur striping		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0010231	transverse fur striping		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0010233	hairless tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0010233	hairless tail		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150618	MGI			PMID:2055107
1557590	Eda	ectodysplasin-A	gene	MP:0012078	abnormal tail ring morphology		IAGP		N	RGD:5509061	20170309	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0013177	abnormal tail tip morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:13103353
1557590	Eda	ectodysplasin-A	gene	MP:0013370	anhidrosis		IAGP		N	RGD:5509061	20141225	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0013370	anhidrosis		IAGP		N	RGD:5509061	20141225	MGI			PMID:2348861
1557590	Eda	ectodysplasin-A	gene	MP:0013371	hypohidrosis		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0013373	increased sebum secretion		IAGP		N	RGD:5509061	20141218	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0013378	increased sebocyte number		IAGP		N	RGD:5509061	20141218	MGI			PMID:14506134
1557590	Eda	ectodysplasin-A	gene	MP:0013478	corneal limbitis		IAGP		N	RGD:5509061	20150205	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0013558	abnormal exocrine gland morphology		IEA		N	RGD:5509061	20150702	MGI			
1557590	Eda	ectodysplasin-A	gene	MP:0013580	abnormal nasal gland morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27590203
1557590	Eda	ectodysplasin-A	gene	MP:0013582	abnormal lateral nasal gland morphology		IAGP		N	RGD:5509061	20170119	MGI			PMID:27590203
1557590	Eda	ectodysplasin-A	gene	MP:0013745	abnormal eyelid margin morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:15972955
1557590	Eda	ectodysplasin-A	gene	MP:0014139	abnormal ectoderm morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:18689798
1557590	Eda	ectodysplasin-A	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557590	Eda	ectodysplasin-A	gene	MP:0030494	abnormal molar root morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:5893447
1557590	Eda	ectodysplasin-A	gene	MP:0030496	taurodontia		IAGP		N	RGD:5509061	20250612	MGI			PMID:36765055
1557592	Cdh12	cadherin 12	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0000116	abnormal tooth development		IEA		N	RGD:5509061	20111116	MGI			
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0001216	abnormal epidermal layer morphology		IEA		N	RGD:5509061	20111116	MGI			
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831472
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20111116	MGI			
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0002819	abnormal dental pulp cavity morphology		IEA		N	RGD:5509061	20111116	MGI			
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21979919
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0009931	abnormal skin appearance		IEA		N	RGD:5509061	20111116	MGI			
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21979919
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21979919
1557593	Map3k11	mitogen-activated protein kinase kinase kinase 11	gene	MP:0011084	lethality at weaning, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20220804	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367666
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367666
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220804	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220804	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367666
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20220811	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20220804	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367666
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367666
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20220804	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367666
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15367666
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220804	MGI			PMID:35312628
1557595	Ndufa13	NADH:ubiquinone oxidoreductase subunit A13	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220811	MGI			PMID:35312628
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0001970	abnormal pain threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:22461625
1557596	Lpar5	lysophosphatidic acid receptor 5	gene	MP:0012306	enhanced spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23039190
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0010762	abnormal microglial cell activation		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1557597	Gpr101	G protein-coupled receptor 101	gene	MP:0020873	abnormal arcuate nucleus of hypothalamus morphology		IAGP		N	RGD:5509061	20260604	MGI			PMID:40655975
1557598	Rasa4	RAS p21 protein activator 4	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16041389
1557598	Rasa4	RAS p21 protein activator 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16041389
1557599	Rcbtb2	regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200618	MGI			PMID:26291700
1557599	Rcbtb2	regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20200618	MGI			PMID:26291700
1557599	Rcbtb2	regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20200618	MGI			PMID:26291700
1557599	Rcbtb2	regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20200618	MGI			PMID:26291700
1557599	Rcbtb2	regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20200618	MGI			PMID:26291700
1557599	Rcbtb2	regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20200618	MGI			PMID:26291700
1557599	Rcbtb2	regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20200618	MGI			PMID:26291700
1557599	Rcbtb2	regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20200618	MGI			PMID:26291700
1557599	Rcbtb2	regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200618	MGI			PMID:26291700
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20170921	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0001324	abnormal eye pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0001688	abnormal somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20240620	MGI			PMID:38671004
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0004470	small nasal bone		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0004476	absent palatine bone		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20240620	MGI			PMID:38671004
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869748
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0008944	decreased sensitivity to induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869748
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0009579	acephaly		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20240620	MGI			PMID:38671004
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240620	MGI			PMID:38671004
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869748
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20150910	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0012240	abnormal hepatoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14744934
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20240620	MGI			PMID:38671004
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0030072	round face		IAGP		N	RGD:5509061	20170921	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:24895408
1557600	Dph1	diphthamide biosynthesis 1	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20221201	MGI			PMID:24895408
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0010393	shortened QRS complex duration		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20210429	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0014390	decreased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:31939735
1557601	Bud23	BUD23, rRNA methyltransferase and ribosome maturation factor	gene	MP:0031718	shortened corrected QT interval		IAGP		N	RGD:5509061	20260514	MGI			PMID:31939735
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0000189	hypoglycemia		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20191219	MGI			PMID:24713655
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417746
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20201015	MGI			PMID:30989113
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20201015	MGI			PMID:30989113
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884037
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884037
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884037
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884037
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884037
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20201015	MGI			PMID:30989113
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417746
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20191107	MGI			PMID:28475869
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20201015	MGI			PMID:30989113
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10686620
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417746
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0003061	decreased aerobic running capacity		IAGP		N	RGD:5509061	20190131	MGI			PMID:28683291
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20191219	MGI			PMID:24713655
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0004069	abnormal muscle spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417746
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20201015	MGI			PMID:30989113
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0005278	abnormal cholesterol homeostasis		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20201015	MGI			PMID:30989113
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20191107	MGI			PMID:28475869
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20191107	MGI			PMID:28475869
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20191107	MGI			PMID:28475869
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0008486	decreased muscle spindle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626887
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884037
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20191219	MGI			PMID:24713655
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0009399	increased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417746
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20191219	MGI			PMID:24713655
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103131
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20191219	MGI			PMID:24713655
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0010238	increased skeletal muscle weight		IAGP		N	RGD:5509061	20191219	MGI			PMID:24713655
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0010239	decreased skeletal muscle weight		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0010398	decreased liver glycogen level		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0010401	increased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20190131	MGI			PMID:28683291
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20190131	MGI			PMID:28683291
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12417746
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0011107	embryonic lethality between somite formation and embryo turning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884037
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0011201	abnormal visceral yolk sac cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884037
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20180927	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0011636	disorganized mitochondrial cristae		IAGP		N	RGD:5509061	20201217	MGI			PMID:31530015
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20190131	MGI			PMID:28683291
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0012735	abnormal response to exercise		IAGP		N	RGD:5509061	20190131	MGI			PMID:28683291
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0014389	decreased skeletal muscle fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:29898916
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0030021	increased muscle cell glucose uptake		IAGP		N	RGD:5509061	20201015	MGI			PMID:30989113
1557603	Myl1	myosin, light polypeptide 1	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20191219	MGI			PMID:24713655
1557608	Synpo2	synaptopodin 2	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1557608	Synpo2	synaptopodin 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1557608	Synpo2	synaptopodin 2	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1557608	Synpo2	synaptopodin 2	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1557608	Synpo2	synaptopodin 2	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1557608	Synpo2	synaptopodin 2	gene	MP:0003896	prolonged PR interval		IEA		N	RGD:5509061	20211021	MGI			
1557608	Synpo2	synaptopodin 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1557608	Synpo2	synaptopodin 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557609	Ap1s3	adaptor-related protein complex AP-1, sigma 3	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20230601	MGI			
1557611	Fundc2	FUN14 domain containing 2	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20210318	MGI			PMID:29786068
1557611	Fundc2	FUN14 domain containing 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:29786068
1557611	Fundc2	FUN14 domain containing 2	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30576423
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0000579	abnormal nail morphology		IEA		N	RGD:5509061	20241121	MGI			
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20240523	MGI			
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20181227	MGI			
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0011392	increased fetal cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557612	Rbpms2	RNA binding protein with multiple splicing 2	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:40602408
1557613	Ano5	anoctamin 5	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1557613	Ano5	anoctamin 5	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1557613	Ano5	anoctamin 5	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1557613	Ano5	anoctamin 5	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20180426	MGI			PMID:26667038
1557613	Ano5	anoctamin 5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20260402	MGI			
1557613	Ano5	anoctamin 5	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0003646	increased muscle fatigability		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0003668	abnormal periodontal ligament morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0004358	bowed tibia		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0005190	osteomyelitis		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1557613	Ano5	anoctamin 5	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0005422	osteosclerosis		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0005601	increased angiogenesis		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0009280	decreased activated sperm motility		IAGP		N	RGD:5509061	20180426	MGI			PMID:26667038
1557613	Ano5	anoctamin 5	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0009414	skeletal muscle fiber necrosis		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0010090	increased circulating creatine kinase level		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0010932	increased trabecular bone connectivity density		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0011642	abnormal bone collagen fibril morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20180426	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0014344	abnormal skeletal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:26911675
1557613	Ano5	anoctamin 5	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20180426	MGI			PMID:26667038
1557613	Ano5	anoctamin 5	gene	MP:0030050	large mandible		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0030050	large mandible		IAGP		N	RGD:5509061	20230629	MGI			PMID:34841576
1557613	Ano5	anoctamin 5	gene	MP:0030132	periodontium inflammation		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0030223	mandibular hyperostosis		IAGP		N	RGD:5509061	20210121	MGI			PMID:30712070
1557613	Ano5	anoctamin 5	gene	MP:0031328	delayed skeletal muscle regeneration		IAGP		N	RGD:5509061	20220106	MGI			PMID:26911675
1557614	Il25	interleukin 25	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606667
1557614	Il25	interleukin 25	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1557614	Il25	interleukin 25	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1557614	Il25	interleukin 25	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1557614	Il25	interleukin 25	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230119	MGI			
1557614	Il25	interleukin 25	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1557614	Il25	interleukin 25	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20260402	MGI			
1557614	Il25	interleukin 25	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20141003	MGI			
1557614	Il25	interleukin 25	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606667
1557614	Il25	interleukin 25	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20154671
1557614	Il25	interleukin 25	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1557614	Il25	interleukin 25	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606668
1557614	Il25	interleukin 25	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1557614	Il25	interleukin 25	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606667
1557614	Il25	interleukin 25	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200411
1557614	Il25	interleukin 25	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606668
1557614	Il25	interleukin 25	gene	MP:0005012	decreased eosinophil cell number		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200411
1557614	Il25	interleukin 25	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606667
1557614	Il25	interleukin 25	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606667
1557614	Il25	interleukin 25	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606668
1557614	Il25	interleukin 25	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606668
1557614	Il25	interleukin 25	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:20154671
1557614	Il25	interleukin 25	gene	MP:0008091	decreased T-helper 2 cell number		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606667
1557614	Il25	interleukin 25	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606668
1557614	Il25	interleukin 25	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606668
1557614	Il25	interleukin 25	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20154671
1557614	Il25	interleukin 25	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20154671
1557614	Il25	interleukin 25	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606668
1557614	Il25	interleukin 25	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20154671
1557614	Il25	interleukin 25	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0008712	decreased interleukin-9 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20154671
1557614	Il25	interleukin 25	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606667
1557614	Il25	interleukin 25	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16606667
1557614	Il25	interleukin 25	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200411
1557614	Il25	interleukin 25	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17200411
1557614	Il25	interleukin 25	gene	MP:0010181	decreased susceptibility to weight loss		IAGP		N	RGD:5509061	20160526	MGI			PMID:25888259
1557614	Il25	interleukin 25	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20231207	MGI			
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367585
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0002356	abnormal spleen red pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12781363
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16096649
1557615	Mllt1	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12367585
1557616	Bmx	BMX non-receptor tyrosine kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416142
1557616	Bmx	BMX non-receptor tyrosine kinase	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21471444
1557617	Nectin4	nectin cell adhesion molecule 4	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1557617	Nectin4	nectin cell adhesion molecule 4	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20250703	MGI			PMID:36457999
1557617	Nectin4	nectin cell adhesion molecule 4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557617	Nectin4	nectin cell adhesion molecule 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557622	Wdr13	WD repeat domain 13	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557622	Wdr13	WD repeat domain 13	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20151119	MGI			PMID:22715406
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0000473	abnormal stomach glandular epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569124
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0001699	increased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569124
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0002271	abnormal pulmonary alveolar duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569124
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0002271	abnormal pulmonary alveolar duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569124
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569124
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0006341	small first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0006343	enlarged first pharyngeal arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569124
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12569124
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0011820	decreased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20150611	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0011934	abnormal branching involved in pancreas development		IAGP		N	RGD:5509061	20141218	MGI			PMID:12917290
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15576403
1557623	Hhip	Hedgehog-interacting protein	gene	MP:0013291	ectopic pancreas		IAGP		N	RGD:5509061	20141218	MGI			PMID:12917290
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20210520	MGI			
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210520	MGI			
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20210520	MGI			
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210826	MGI			
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1557624	Syncrip	synaptotagmin binding, cytoplasmic RNA interacting protein	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210520	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0000531	right pulmonary isomerism		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0000644	dextrocardia		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0000650	mesocardia		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581775
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581775
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23706739
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581775
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581775
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0006123	tricuspid valve atresia		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581775
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581775
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16581775
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23706739
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0011665	d-loop transposition of the great arteries		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0011668	double outlet right ventricle, Taussig bing type		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20210218	MGI			
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:23706739
1557625	Psme4	proteasome (prosome, macropain) activator subunit 4	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20180301	MGI			PMID:16581775
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230330	MGI			PMID:32665638
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230420	MGI			PMID:36930220
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0003064	decreased coping response		IEA		N	RGD:5509061	20210128	MGI			
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20230420	MGI			PMID:36930220
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20230330	MGI			PMID:32665638
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20230420	MGI			PMID:36930220
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20230420	MGI			PMID:36930220
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20230330	MGI			PMID:32665638
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20230420	MGI			PMID:36930220
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20230420	MGI			PMID:36930220
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:32665638
1557626	Adad2	adenosine deaminase domain containing 2	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20230803	MGI			PMID:36698249
1557627	Ranbp3	RAN binding protein 3	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1557627	Ranbp3	RAN binding protein 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1557629	Zfp92	zinc finger protein 92	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1557629	Zfp92	zinc finger protein 92	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1557629	Zfp92	zinc finger protein 92	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1557629	Zfp92	zinc finger protein 92	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1557629	Zfp92	zinc finger protein 92	gene	MP:0010768	mortality/aging		IAGP		N	RGD:5509061	20210701	MGI			PMID:33653874
1557630	St6galnac2	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557630	St6galnac2	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557630	St6galnac2	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557630	St6galnac2	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557630	St6galnac2	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557630	St6galnac2	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557630	St6galnac2	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557630	St6galnac2	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557631	Cep192	centrosomal protein 192	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1557631	Cep192	centrosomal protein 192	gene	MP:0008823	abnormal interventricular septum membranous part morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1557631	Cep192	centrosomal protein 192	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1557631	Cep192	centrosomal protein 192	gene	MP:0010498	abnormal interventricular septum muscular part morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:36325906
1557632	Fem1a	fem 1 homolog a	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26439841
1557632	Fem1a	fem 1 homolog a	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:26439841
1557632	Fem1a	fem 1 homolog a	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180503	MGI			PMID:26439841
1557632	Fem1a	fem 1 homolog a	gene	MP:0003269	colon polyps		IAGP		N	RGD:5509061	20180503	MGI			PMID:26439841
1557632	Fem1a	fem 1 homolog a	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20180503	MGI			PMID:26439841
1557632	Fem1a	fem 1 homolog a	gene	MP:0012436	increased colon tumor incidence		IAGP		N	RGD:5509061	20180503	MGI			PMID:26439841
1557632	Fem1a	fem 1 homolog a	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20180503	MGI			PMID:26439841
1557632	Fem1a	fem 1 homolog a	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20180503	MGI			PMID:26439841
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539826
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539826
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539826
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0003729	abnormal photoreceptor outer segment morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0008582	short photoreceptor inner segment		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0009772	abnormal retina development		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539826
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21539826
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15755804
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0014059	abnormal photoreceptor connecting cilium morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0020384	absent kidney epithelial cell primary cilium		IAGP		N	RGD:5509061	20180222	MGI			PMID:27153923
1557633	Arl13b	ADP-ribosylation factor-like 13B	gene	MP:0020813	abnormal photoreceptor outer segment disc membrane morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:30573647
1557635	Hs6st2	heparan sulfate 6-O-sulfotransferase 2	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18281280
1557635	Hs6st2	heparan sulfate 6-O-sulfotransferase 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557636	Cd300c2	CD300C molecule 2	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21727189
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20170105	MGI			
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0001175	abnormal lung morphology		IEA		N	RGD:5509061	20170105	MGI			
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20170105	MGI			
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20170105	MGI			
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20221215	MGI			
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20170105	MGI			
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20170105	MGI			
1557637	Hook3	hook microtubule tethering protein 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20170105	MGI			
1557638	Acsbg1	acyl-CoA synthetase bubblegum family member 1	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19167491
1557638	Acsbg1	acyl-CoA synthetase bubblegum family member 1	gene	MP:0002786	abnormal Leydig cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19167491
1557638	Acsbg1	acyl-CoA synthetase bubblegum family member 1	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:19167491
1557638	Acsbg1	acyl-CoA synthetase bubblegum family member 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19167491
1557638	Acsbg1	acyl-CoA synthetase bubblegum family member 1	gene	MP:0005282	decreased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19167491
1557639	Ciapin1	cytokine induced apoptosis inhibitor 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970183
1557639	Ciapin1	cytokine induced apoptosis inhibitor 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970183
1557639	Ciapin1	cytokine induced apoptosis inhibitor 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970183
1557639	Ciapin1	cytokine induced apoptosis inhibitor 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970183
1557639	Ciapin1	cytokine induced apoptosis inhibitor 1	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970183
1557639	Ciapin1	cytokine induced apoptosis inhibitor 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970183
1557639	Ciapin1	cytokine induced apoptosis inhibitor 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970183
1557639	Ciapin1	cytokine induced apoptosis inhibitor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970183
1557639	Ciapin1	cytokine induced apoptosis inhibitor 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14970183
1557640	Ddx18	DEAD box helicase 18	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20250508	MGI			
1557640	Ddx18	DEAD box helicase 18	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20240523	MGI			
1557640	Ddx18	DEAD box helicase 18	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20210506	MGI			PMID:31914400
1557640	Ddx18	DEAD box helicase 18	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:31914400
1557640	Ddx18	DEAD box helicase 18	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20241017	MGI			PMID:31914400
1557640	Ddx18	DEAD box helicase 18	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241017	MGI			
1557640	Ddx18	DEAD box helicase 18	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20240523	MGI			
1557640	Ddx18	DEAD box helicase 18	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20210506	MGI			PMID:31914400
1557640	Ddx18	DEAD box helicase 18	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1557640	Ddx18	DEAD box helicase 18	gene	MP:0012111	failure of morula compaction		IEA		N	RGD:5509061	20241017	MGI			
1557643	Susd4	sushi domain containing 4	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0010050	hypermyelination		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0011566	abnormal complement protein level		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0020358	abnormal inhibitory synapse morphology		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557643	Susd4	sushi domain containing 4	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20210722	MGI			PMID:32179479
1557644	Ptx3	pentraxin related gene	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040004
1557644	Ptx3	pentraxin related gene	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:14998931
1557644	Ptx3	pentraxin related gene	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432394
1557644	Ptx3	pentraxin related gene	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432394
1557644	Ptx3	pentraxin related gene	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040004
1557644	Ptx3	pentraxin related gene	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432394
1557644	Ptx3	pentraxin related gene	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14998931
1557644	Ptx3	pentraxin related gene	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040004
1557644	Ptx3	pentraxin related gene	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14998931
1557644	Ptx3	pentraxin related gene	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040004
1557644	Ptx3	pentraxin related gene	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14998931
1557644	Ptx3	pentraxin related gene	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432394
1557644	Ptx3	pentraxin related gene	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432394
1557644	Ptx3	pentraxin related gene	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432394
1557644	Ptx3	pentraxin related gene	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432394
1557644	Ptx3	pentraxin related gene	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432394
1557644	Ptx3	pentraxin related gene	gene	MP:0005465	abnormal T-helper 1 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12432394
1557644	Ptx3	pentraxin related gene	gene	MP:0009372	abnormal cumulus oophorus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040004
1557644	Ptx3	pentraxin related gene	gene	MP:0009372	abnormal cumulus oophorus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14998931
1557644	Ptx3	pentraxin related gene	gene	MP:0009374	absent cumulus expansion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040004
1557644	Ptx3	pentraxin related gene	gene	MP:0009374	absent cumulus expansion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14998931
1557644	Ptx3	pentraxin related gene	gene	MP:0009374	absent cumulus expansion		IAGP		N	RGD:5509061	20230518	MGI			PMID:17675295
1557644	Ptx3	pentraxin related gene	gene	MP:0020949	increased susceptibility to Coronaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:22732935
1557644	Ptx3	pentraxin related gene	gene	MP:0031420	decreased superovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:12040004
1557646	Ssu2	ssu-2 homolog	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:27680507
1557646	Ssu2	ssu-2 homolog	gene	MP:0002818	abnormal dentin morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:27680507
1557646	Ssu2	ssu-2 homolog	gene	MP:0002819	abnormal dental pulp cavity morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:27680507
1557646	Ssu2	ssu-2 homolog	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20241121	MGI			
1557646	Ssu2	ssu-2 homolog	gene	MP:0013250	abnormal dental pulp morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:27680507
1557646	Ssu2	ssu-2 homolog	gene	MP:0030451	abnormal dentin mineralization		IAGP		N	RGD:5509061	20171221	MGI			PMID:27680507
1557646	Ssu2	ssu-2 homolog	gene	MP:0030455	increased odontoblast number		IAGP		N	RGD:5509061	20180215	MGI			PMID:27680507
1557646	Ssu2	ssu-2 homolog	gene	MP:0030459	abnormal tooth attrition		IAGP		N	RGD:5509061	20180215	MGI			PMID:27680507
1557646	Ssu2	ssu-2 homolog	gene	MP:0030543	abnormal predentin morphology		IAGP		N	RGD:5509061	20180215	MGI			PMID:27680507
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20150212	MGI			PMID:24132636
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0000350	abnormal cell proliferation		IAGP		N	RGD:5509061	20180222	MGI			PMID:28783163
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20231102	MGI			PMID:37628941
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20231102	MGI			PMID:19763165
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20231102	MGI			PMID:19763165
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20231102	MGI			PMID:37628941
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20231102	MGI			PMID:37628941
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20231102	MGI			PMID:19763165
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20150212	MGI			PMID:24132636
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20150212	MGI			PMID:24132636
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20180222	MGI			PMID:28783163
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20231102	MGI			PMID:19763165
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20231102	MGI			PMID:19763165
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20231102	MGI			PMID:37628941
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20231102	MGI			PMID:37628941
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20231102	MGI			PMID:19763165
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20231102	MGI			PMID:37628941
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0006321	increased myocardial fiber number		IAGP		N	RGD:5509061	20180222	MGI			PMID:28783163
1557651	Tnni3k	TNNI3 interacting kinase	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231102	MGI			PMID:37628941
1557652	Hoxa3	homeobox A3	gene	MP:0000078	abnormal supraoccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0000079	abnormal basioccipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0000678	abnormal parathyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0000680	absent parathyroid glands		IAGP		N	RGD:5509061	20150305	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1557652	Hoxa3	homeobox A3	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557652	Hoxa3	homeobox A3	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0000705	athymia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7913519
1557652	Hoxa3	homeobox A3	gene	MP:0000966	decreased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14960494
1557652	Hoxa3	homeobox A3	gene	MP:0001051	abnormal somatic motor system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12954718
1557652	Hoxa3	homeobox A3	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0001073	abnormal glossopharyngeal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557652	Hoxa3	homeobox A3	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557652	Hoxa3	homeobox A3	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002132	abnormal respiratory system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002249	abnormal larynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002256	abnormal laryngeal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002258	abnormal cricoid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002282	abnormal trachea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16696966
1557652	Hoxa3	homeobox A3	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0002951	small thyroid gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0003007	ectopic thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1557652	Hoxa3	homeobox A3	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10688203
1557652	Hoxa3	homeobox A3	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0003154	abnormal soft palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0003445	sirenomelia		IAGP		N	RGD:5509061	20150716	MGI			PMID:23028455
1557652	Hoxa3	homeobox A3	gene	MP:0003494	parathyroid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0003955	abnormal ultimobranchial body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0003955	abnormal ultimobranchial body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1557652	Hoxa3	homeobox A3	gene	MP:0004136	abnormal tongue muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0004445	small exoccipital bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0004549	small trachea		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0004568	fusion of glossopharyngeal and vagus nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0004568	fusion of glossopharyngeal and vagus nerve		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0004914	absent ultimobranchial body		IAGP		N	RGD:5509061	20150122	MGI			PMID:9520319
1557652	Hoxa3	homeobox A3	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0005298	abnormal clavicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0005406	abnormal heart size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12954718
1557652	Hoxa3	homeobox A3	gene	MP:0006117	aortic valve stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0006340	abnormal fourth pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0006354	abnormal fourth pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0009052	anal stenosis		IAGP		N	RGD:5509061	20150716	MGI			PMID:23028455
1557652	Hoxa3	homeobox A3	gene	MP:0009252	absent urinary bladder		IAGP		N	RGD:5509061	20150716	MGI			PMID:23028455
1557652	Hoxa3	homeobox A3	gene	MP:0009844	abnormal neural crest cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0009913	abnormal hyoid bone greater horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0009913	abnormal hyoid bone greater horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0009915	absent hyoid bone lesser horns		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0009915	absent hyoid bone lesser horns		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0010371	abnormal epiglottis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0010441	total anomalous pulmonary venous connection		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
1557652	Hoxa3	homeobox A3	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0010527	bicuspid pulmonary valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0010541	aorta hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0010548	abnormal dorsal mesocardium morphology		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
1557652	Hoxa3	homeobox A3	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0011576	absent cervical atlas		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0011683	dual inferior vena cava		IAGP		N	RGD:5509061	20231109	MGI			PMID:20071345
1557652	Hoxa3	homeobox A3	gene	MP:0012491	larynx stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1673020
1557652	Hoxa3	homeobox A3	gene	MP:0013162	abnormal thyroid gland isthmus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0013162	abnormal thyroid gland isthmus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1557652	Hoxa3	homeobox A3	gene	MP:0013163	absent thyroid gland isthmus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0013163	absent thyroid gland isthmus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9520319
1557652	Hoxa3	homeobox A3	gene	MP:0013290	persistent ultimobranchial bodies		IAGP		N	RGD:5509061	20150122	MGI			PMID:9520319
1557652	Hoxa3	homeobox A3	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20150305	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20150305	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0013574	ectopic parathyroid gland		IAGP		N	RGD:5509061	20150305	MGI			PMID:9520319
1557652	Hoxa3	homeobox A3	gene	MP:0030291	short soft palate		IAGP		N	RGD:5509061	20171102	MGI			PMID:20498049
1557652	Hoxa3	homeobox A3	gene	MP:0030337	enlarged third pharyngeal arch artery		IAGP		N	RGD:5509061	20171116	MGI			PMID:14623825
1557652	Hoxa3	homeobox A3	gene	MP:0030869	thyroid cartilage hypoplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:9441667
1557652	Hoxa3	homeobox A3	gene	MP:0030872	small cricoid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:9441667
1557655	Sympk	symplekin	gene	MP:0001577	anemia		IEA		N	RGD:5509061	20111116	MGI			
1557655	Sympk	symplekin	gene	MP:0002192	hydrops fetalis		IEA		N	RGD:5509061	20111116	MGI			
1557655	Sympk	symplekin	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1557656	Onecut2	one cut domain, family member 2	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103213
1557656	Onecut2	one cut domain, family member 2	gene	MP:0002929	abnormal bile duct development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103213
1557656	Onecut2	one cut domain, family member 2	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17400205
1557656	Onecut2	one cut domain, family member 2	gene	MP:0012242	abnormal hepatoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103213
1557656	Onecut2	one cut domain, family member 2	gene	MP:0012246	abnormal hepatic cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16103213
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0001243	abnormal dermal layer morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0009545	abnormal dermis papillary layer morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557657	Gorab	golgin, RAB6-interacting	gene	MP:0013205	abnormal nonmotile primary cilium morphology		IAGP		N	RGD:5509061	20160707	MGI			PMID:26967474
1557658	Dnajc5b	DnaJ heat shock protein family (Hsp40) member C5 beta	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1557658	Dnajc5b	DnaJ heat shock protein family (Hsp40) member C5 beta	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20160421	MGI			
1557658	Dnajc5b	DnaJ heat shock protein family (Hsp40) member C5 beta	gene	MP:0010571	shortened ST segment		IEA		N	RGD:5509061	20210128	MGI			
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20170330	MGI			PMID:27821757
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20200514	MGI			
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20200514	MGI			
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20200514	MGI			
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20160204	MGI			PMID:24586788
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:24586788
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20160204	MGI			PMID:24586788
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20160204	MGI			PMID:24586788
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20170330	MGI			PMID:27821757
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:24586788
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20200514	MGI			
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20170330	MGI			PMID:27821757
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20160204	MGI			PMID:24586788
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0009661	abnormal pregnancy		IAGP		N	RGD:5509061	20170330	MGI			PMID:27821757
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0010695	abnormal blood pressure regulation		IAGP		N	RGD:5509061	20160204	MGI			PMID:24586788
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0010935	increased airway resistance		IEA		N	RGD:5509061	20250508	MGI			
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0011320	abnormal glomerular capillary morphology		IAGP		N	RGD:5509061	20170330	MGI			PMID:27821757
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20170330	MGI			PMID:27821757
1557659	Asb4	ankyrin repeat and SOCS box-containing 4	gene	MP:0020153	abnormal urine albumin level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24586788
1557661	Scrn1	secernin 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1557661	Scrn1	secernin 1	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:270322
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:544312
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:892445
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000372	irregular coat pigmentation		IEA		N	RGD:5509061	20181011	MGI			
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2622338
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20150618	MGI			PMID:9799834
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23415220
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:892445
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000405	abnormal auchene hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23415220
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000408	absent duvet hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:892445
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000411	shiny fur		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:2622338
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:2622338
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17148670
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:2622338
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:23415220
1557662	Edar	ectodysplasin-A receptor	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:2622338
1557662	Edar	ectodysplasin-A receptor	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:544312
1557662	Edar	ectodysplasin-A receptor	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20150618	MGI			PMID:9799834
1557662	Edar	ectodysplasin-A receptor	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:17148670
1557662	Edar	ectodysplasin-A receptor	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:892445
1557662	Edar	ectodysplasin-A receptor	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:270322
1557662	Edar	ectodysplasin-A receptor	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:544312
1557662	Edar	ectodysplasin-A receptor	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17148670
1557662	Edar	ectodysplasin-A receptor	gene	MP:0003791	abnormal minor salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20969842
1557662	Edar	ectodysplasin-A receptor	gene	MP:0003849	greasy coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:2622338
1557662	Edar	ectodysplasin-A receptor	gene	MP:0003931	absent molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:270322
1557662	Edar	ectodysplasin-A receptor	gene	MP:0003931	absent molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:544312
1557662	Edar	ectodysplasin-A receptor	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:270322
1557662	Edar	ectodysplasin-A receptor	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:544312
1557662	Edar	ectodysplasin-A receptor	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:892445
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17148670
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006236	absent Meibomian glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:2622338
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006236	absent Meibomian glands		IAGP		N	RGD:5509061	20150618	MGI			PMID:9799834
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006258	abnormal circumvallate papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20969842
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006363	absent auchene hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:892445
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:17148670
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:2622338
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:892445
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006366	absent zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:17148670
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006366	absent zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:892445
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006367	absent sweat gland		IAGP		N	RGD:5509061	20150618	MGI			PMID:9799834
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:270322
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:544312
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:270322
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:544312
1557662	Edar	ectodysplasin-A receptor	gene	MP:0008904	abnormal mammary fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23415220
1557662	Edar	ectodysplasin-A receptor	gene	MP:0009003	abnormal vibrissa number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0009003	abnormal vibrissa number		IAGP		N	RGD:5509061	20141003	MGI			PMID:544312
1557662	Edar	ectodysplasin-A receptor	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20231207	MGI			
1557662	Edar	ectodysplasin-A receptor	gene	MP:0009533	absent palatine gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:20969842
1557662	Edar	ectodysplasin-A receptor	gene	MP:0009534	absent anterior lingual gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:20969842
1557662	Edar	ectodysplasin-A receptor	gene	MP:0010233	hairless tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0010233	hairless tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:892445
1557662	Edar	ectodysplasin-A receptor	gene	MP:0010864	abnormal enamel knot morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19340299
1557662	Edar	ectodysplasin-A receptor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1557662	Edar	ectodysplasin-A receptor	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557662	Edar	ectodysplasin-A receptor	gene	MP:0013176	abnormal tail position or orientation		IEA		N	RGD:5509061	20141003	MGI			
1557662	Edar	ectodysplasin-A receptor	gene	MP:0013457	increased eccrine gland number		IAGP		N	RGD:5509061	20150212	MGI			PMID:23415220
1557662	Edar	ectodysplasin-A receptor	gene	MP:0013458	decreased eccrine gland number		IAGP		N	RGD:5509061	20150212	MGI			PMID:23415220
1557662	Edar	ectodysplasin-A receptor	gene	MP:0030079	small incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:270322
1557662	Edar	ectodysplasin-A receptor	gene	MP:0030079	small incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:5361555
1557662	Edar	ectodysplasin-A receptor	gene	MP:0030079	small incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:544312
1557662	Edar	ectodysplasin-A receptor	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:270322
1557662	Edar	ectodysplasin-A receptor	gene	MP:0030494	abnormal molar root morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:270322
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20210311	MGI			PMID:29895858
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210311	MGI			PMID:29895858
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20210311	MGI			PMID:29895858
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20210311	MGI			PMID:29895858
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20160304	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20260402	MGI			
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0014040	increased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20210311	MGI			PMID:29895858
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20210311	MGI			PMID:29895858
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0014619	absent spermatogonia		IAGP		N	RGD:5509061	20250213	MGI			PMID:19561169
1557665	Fancm	Fanconi anemia, complementation group M	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1557666	Golgb1	golgin B1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180503	MGI			PMID:27226319
1557666	Golgb1	golgin B1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20180503	MGI			PMID:28509431
1557666	Golgb1	golgin B1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:28509431
1557666	Golgb1	golgin B1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20180503	MGI			PMID:28509431
1557666	Golgb1	golgin B1	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20180503	MGI			PMID:28509431
1557666	Golgb1	golgin B1	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20180503	MGI			PMID:27226319
1557666	Golgb1	golgin B1	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20180503	MGI			PMID:27226319
1557666	Golgb1	golgin B1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20230302	MGI			PMID:27226319
1557666	Golgb1	golgin B1	gene	MP:0014430	decreased hyaluronic acid level		IAGP		N	RGD:5509061	20240425	MGI			PMID:27226319
1557666	Golgb1	golgin B1	gene	MP:0031443	abnormal tongue position		IAGP		N	RGD:5509061	20221027	MGI			PMID:27226319
1557666	Golgb1	golgin B1	gene	MP:0031462	decreased palatal shelf size		IAGP		N	RGD:5509061	20230302	MGI			PMID:27226319
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421466
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421466
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723547
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368430
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421466
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368430
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368430
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368430
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723547
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22723547
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421466
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368430
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421466
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368430
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421466
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20421466
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368430
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368430
1557669	Timd4	T cell immunoglobulin and mucin domain containing 4	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20368430
1557670	Phf21a	PHD finger protein 21A	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16684532
1557670	Phf21a	PHD finger protein 21A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16684532
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20250508	MGI			
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0000091	short premaxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20250508	MGI			
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001121	uterus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210826	MGI			
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21204784
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21204784
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20260402	MGI			
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0005536	decreased Leydig cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0006418	abnormal testis cord formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0008869	anovulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0009370	decreased theca cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20241121	MGI			
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056881
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0021213	complete cleft palate		IAGP		N	RGD:5509061	20221201	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0030018	increased cardiac muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:21204784
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0030189	broad snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:17143286
1557672	Plekha1	pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:21204784
1557673	Tprn	taperin	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1557673	Tprn	taperin	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1557673	Tprn	taperin	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20170601	MGI			PMID:27693694
1557673	Tprn	taperin	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20170601	MGI			PMID:27693694
1557673	Tprn	taperin	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20170601	MGI			PMID:27693694
1557673	Tprn	taperin	gene	MP:0004534	decreased inner hair cell stereocilia number		IAGP		N	RGD:5509061	20170601	MGI			PMID:27693694
1557673	Tprn	taperin	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1557673	Tprn	taperin	gene	MP:0004749	nonsyndromic hearing loss		IAGP		N	RGD:5509061	20170803	MGI			PMID:27693694
1557673	Tprn	taperin	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1557673	Tprn	taperin	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20170601	MGI			PMID:27693694
1557674	Tulp3	TUB like protein 3	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0002809	increased spinal cord size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1557674	Tulp3	TUB like protein 3	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1557674	Tulp3	TUB like protein 3	gene	MP:0004083	polysyndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
1557674	Tulp3	TUB like protein 3	gene	MP:0005297	spina bifida occulta		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1557674	Tulp3	TUB like protein 3	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20210128	MGI			
1557674	Tulp3	TUB like protein 3	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0006253	clinodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20160421	MGI			
1557674	Tulp3	TUB like protein 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1557674	Tulp3	TUB like protein 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557674	Tulp3	TUB like protein 3	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557674	Tulp3	TUB like protein 3	gene	MP:0012544	abnormal caudal neuropore morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0012547	spina bifida cystica		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0012701	increased embryonic neuroepithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11406614
1557674	Tulp3	TUB like protein 3	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19223390
1557674	Tulp3	TUB like protein 3	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1557674	Tulp3	TUB like protein 3	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IAGP		N	RGD:5509061	20200310	MGI			PMID:30799240
1557675	Thyn1	thymocyte nuclear protein 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:31329649
1557677	Btbd2	BTB domain containing 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20240523	MGI			
1557677	Btbd2	BTB domain containing 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1557677	Btbd2	BTB domain containing 2	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210128	MGI			
1557677	Btbd2	BTB domain containing 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1557677	Btbd2	BTB domain containing 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1557677	Btbd2	BTB domain containing 2	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201231	MGI			
1557677	Btbd2	BTB domain containing 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1557677	Btbd2	BTB domain containing 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20181227	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20201231	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20200402	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20200402	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:26405179
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20200402	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:26405179
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20170706	MGI			PMID:26405179
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20170706	MGI			PMID:26405179
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0006241	abnormal placement of pupils		IEA		N	RGD:5509061	20200402	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0012040	abnormal c-wave shape		IAGP		N	RGD:5509061	20170706	MGI			PMID:26405179
1557679	Adamtsl4	ADAMTS-like 4	gene	MP:0031428	lens dislocation		IAGP		N	RGD:5509061	20220714	MGI			PMID:26405179
1557680	Mapkapk5	MAP kinase-activated protein kinase 5	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254968
1557680	Mapkapk5	MAP kinase-activated protein kinase 5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254968
1557680	Mapkapk5	MAP kinase-activated protein kinase 5	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14560018
1557680	Mapkapk5	MAP kinase-activated protein kinase 5	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254968
1557680	Mapkapk5	MAP kinase-activated protein kinase 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557680	Mapkapk5	MAP kinase-activated protein kinase 5	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17254968
1557682	Angptl3	angiopoietin-like 3	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788823
1557682	Angptl3	angiopoietin-like 3	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788823
1557682	Angptl3	angiopoietin-like 3	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508209
1557682	Angptl3	angiopoietin-like 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20221103	MGI			
1557682	Angptl3	angiopoietin-like 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1557682	Angptl3	angiopoietin-like 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1557682	Angptl3	angiopoietin-like 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788823
1557682	Angptl3	angiopoietin-like 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1557682	Angptl3	angiopoietin-like 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508209
1557682	Angptl3	angiopoietin-like 3	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19318355
1557682	Angptl3	angiopoietin-like 3	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788823
1557682	Angptl3	angiopoietin-like 3	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508209
1557682	Angptl3	angiopoietin-like 3	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508209
1557682	Angptl3	angiopoietin-like 3	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20221103	MGI			
1557682	Angptl3	angiopoietin-like 3	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788823
1557682	Angptl3	angiopoietin-like 3	gene	MP:0005146	decreased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508209
1557682	Angptl3	angiopoietin-like 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788823
1557682	Angptl3	angiopoietin-like 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1557682	Angptl3	angiopoietin-like 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508209
1557682	Angptl3	angiopoietin-like 3	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19318355
1557682	Angptl3	angiopoietin-like 3	gene	MP:0005318	decreased triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788823
1557682	Angptl3	angiopoietin-like 3	gene	MP:0009283	decreased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788823
1557682	Angptl3	angiopoietin-like 3	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16508209
1557682	Angptl3	angiopoietin-like 3	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20221103	MGI			
1557682	Angptl3	angiopoietin-like 3	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1557682	Angptl3	angiopoietin-like 3	gene	MP:0011578	increased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11788823
1557682	Angptl3	angiopoietin-like 3	gene	MP:0011578	increased lipoprotein lipase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16081640
1557682	Angptl3	angiopoietin-like 3	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20221103	MGI			
1557686	Fam107b	family with sequence similarity 107, member B	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20160804	MGI			
1557686	Fam107b	family with sequence similarity 107, member B	gene	MP:0000452	abnormal mouth morphology		IEA		N	RGD:5509061	20160804	MGI			
1557686	Fam107b	family with sequence similarity 107, member B	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1557686	Fam107b	family with sequence similarity 107, member B	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1557686	Fam107b	family with sequence similarity 107, member B	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20250904	MGI			PMID:33807672
1557689	Armcx3	armadillo repeat containing, X-linked 3	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20240328	MGI			PMID:33807672
1557690	Rab7b	RAB7B, member RAS oncogene family	gene	MP:0005058	abnormal lysosome morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:34494097
1557690	Rab7b	RAB7B, member RAS oncogene family	gene	MP:0020349	abnormal dendritic cell migration		IAGP		N	RGD:5509061	20220331	MGI			PMID:34494097
1557691	Bcl2l14	BCL2 like 14	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201119	MGI			PMID:23059823
1557691	Bcl2l14	BCL2 like 14	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20201119	MGI			PMID:31296963
1557691	Bcl2l14	BCL2 like 14	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20201119	MGI			PMID:31296963
1557691	Bcl2l14	BCL2 like 14	gene	MP:0012436	increased colon tumor incidence		IAGP		N	RGD:5509061	20201119	MGI			PMID:31296963
1557691	Bcl2l14	BCL2 like 14	gene	MP:0013296	abnormal susceptibility to induced colitis		IAGP		N	RGD:5509061	20201119	MGI			PMID:31296963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:28172500
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21597012
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000301	decreased atrioventricular cushion size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15166096
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:33773996
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:34767447
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21597012
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0003865	lymph node inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004111	abnormal coronary artery morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004791	absent lower incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20240530	MGI			PMID:32986812
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20240530	MGI			PMID:32986812
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0005673	decreased susceptibility to graft versus host disease		IAGP		N	RGD:5509061	20240530	MGI			PMID:32986812
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0006047	aortic valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0006049	semilunar valve regurgitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15166096
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0006120	mitral valve prolapse		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21597012
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20240530	MGI			PMID:32986812
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20240530	MGI			PMID:32986812
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008686	abnormal interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20240530	MGI			PMID:32986812
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9462518
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20190912	MGI			PMID:28172500
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0008825	abnormal cardiac epithelial to mesenchymal transition		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0009382	abnormal cardiac jelly morphology		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010414	partial atrioventricular septal defect		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010453	abnormal coronary vein morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010482	abnormal aortic sinus morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010593	thick aortic valve cusps		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010594	thick aortic valve		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010595	abnormal aortic valve cusp morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010597	absent aortic valve cusps		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010601	thick pulmonary valve		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010604	absent pulmonary valve cusps		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010614	abnormal mitral valve cusp morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010614	abnormal mitral valve cusp morphology		IAGP		N	RGD:5509061	20240104	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010622	abnormal tricuspid valve cusp morphology		IAGP		N	RGD:5509061	20240104	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010656	thick myocardium		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22573816
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178125
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824573
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515964
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190307	MGI			PMID:25625206
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0011648	thick heart valve cusps		IAGP		N	RGD:5509061	20160107	MGI			PMID:26100917
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0013206	abnormal motile cilium morphology		IAGP		N	RGD:5509061	20210715	MGI			PMID:31118289
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0013241	embryo tissue necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20260402	MGI			
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:21464221
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0030083	long upper incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0030089	short lower incisors		IAGP		N	RGD:5509061	20170928	MGI			PMID:18846253
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0030992	atrioventricular cushion hypoplasia		IAGP		N	RGD:5509061	20231207	MGI			PMID:33846290
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0031551	abnormal mitral valve development		IAGP		N	RGD:5509061	20240104	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0031552	abnormal tricuspid valve development		IAGP		N	RGD:5509061	20240104	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0031553	abnormal semilunar valve development		IAGP		N	RGD:5509061	20240104	MGI			PMID:9515963
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0031572	small atrioventricular valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:23824573
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0031582	small semilunar valve		IAGP		N	RGD:5509061	20240125	MGI			PMID:23824573
1557692	Nfatc1	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1	gene	MP:0031593	decreased cardiac jelly amount		IAGP		N	RGD:5509061	20240229	MGI			PMID:25625206
1557693	Dock4	dedicator of cytokinesis 4	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20260402	MGI			
1557693	Dock4	dedicator of cytokinesis 4	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20230119	MGI			
1557693	Dock4	dedicator of cytokinesis 4	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20230119	MGI			
1557693	Dock4	dedicator of cytokinesis 4	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20260402	MGI			
1557693	Dock4	dedicator of cytokinesis 4	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20160616	MGI			PMID:26129894
1557693	Dock4	dedicator of cytokinesis 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20160616	MGI			PMID:26129894
1557693	Dock4	dedicator of cytokinesis 4	gene	MP:0020373	abnormal blood vessel lumen formation		IAGP		N	RGD:5509061	20170713	MGI			PMID:26129894
1557693	Dock4	dedicator of cytokinesis 4	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20260402	MGI			
1557694	Zfp296	zinc finger protein 296	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0008391	abnormal primordial germ cell morphology		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0008995	early reproductive senescence		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190404	MGI			PMID:28963472
1557694	Zfp296	zinc finger protein 296	gene	MP:0030934	decreased primordial germ cell proliferation		IAGP		N	RGD:5509061	20190411	MGI			PMID:28963472
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746429
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20403327
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0000410	waved hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:20403327
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20403327
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250484
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20403327
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:20403327
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746429
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250484
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250484
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746429
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20403327
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0003454	erythroderma		IAGP		N	RGD:5509061	20141003	MGI			PMID:20403327
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0003663	abnormal thermosensation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15746429
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20403327
1557695	Trpv3	transient receptor potential cation channel, subfamily V, member 3	gene	MP:0009594	abnormal corneocyte envelope morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20403327
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645526
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645526
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645526
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645526
1557696	Siah1a	siah E3 ubiquitin protein ligase 1A	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11884614
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002700	increased opacity of vitreous body		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0003062	abnormal coping response		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0003643	spleen atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20141003	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0004647	decreased lumbar vertebrae number		IEA		N	RGD:5509061	20141003	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19861679
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0008821	increased blood uric acid level		IEA		N	RGD:5509061	20160804	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0009859	eye opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20141003	MGI			
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0010178	increased number of Howell-Jolly bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24218140
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24255920
1557697	Asxl1	ASXL transcriptional regulator 1	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557698	Itm2b	integral membrane protein 2B	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098268
1557698	Itm2b	integral membrane protein 2B	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098268
1557698	Itm2b	integral membrane protein 2B	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:18753367
1557698	Itm2b	integral membrane protein 2B	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048150
1557698	Itm2b	integral membrane protein 2B	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21048150
1557698	Itm2b	integral membrane protein 2B	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098268
1557698	Itm2b	integral membrane protein 2B	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:21048150
1557698	Itm2b	integral membrane protein 2B	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:21048150
1557698	Itm2b	integral membrane protein 2B	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:21098268
1557703	Ier5l	immediate early response 5-like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220811	MGI			
1557703	Ier5l	immediate early response 5-like	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220811	MGI			
1557703	Ier5l	immediate early response 5-like	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220811	MGI			
1557703	Ier5l	immediate early response 5-like	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20260402	MGI			
1557703	Ier5l	immediate early response 5-like	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1557703	Ier5l	immediate early response 5-like	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20250508	MGI			
1557703	Ier5l	immediate early response 5-like	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1557703	Ier5l	immediate early response 5-like	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210826	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210520	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20200402	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210520	MGI			
1557704	Hdgfl3	HDGF like 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20220519	MGI			
1557707	Clxn	calaxin	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0004132	absent embryonic cilia		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0008933	abnormal motile primary cilium physiology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557707	Clxn	calaxin	gene	MP:0013197	decreased embryonic cilium number		IAGP		N	RGD:5509061	20190919	MGI			PMID:31240264
1557708	Ablim3	actin binding LIM protein family, member 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1557708	Ablim3	actin binding LIM protein family, member 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20250508	MGI			
1557708	Ablim3	actin binding LIM protein family, member 3	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20220519	MGI			
1557708	Ablim3	actin binding LIM protein family, member 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1557708	Ablim3	actin binding LIM protein family, member 3	gene	MP:0002607	decreased basophil cell number		IEA		N	RGD:5509061	20221215	MGI			
1557708	Ablim3	actin binding LIM protein family, member 3	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20221215	MGI			
1557708	Ablim3	actin binding LIM protein family, member 3	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1557708	Ablim3	actin binding LIM protein family, member 3	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1557709	Galp	galanin-like peptide	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775887
1557709	Galp	galanin-like peptide	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775887
1557709	Galp	galanin-like peptide	gene	MP:0011957	decreased compensatory feeding amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18775887
1557710	Etfb	electron transferring flavoprotein, beta polypeptide	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230601	MGI			
1557710	Etfb	electron transferring flavoprotein, beta polypeptide	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230601	MGI			
1557710	Etfb	electron transferring flavoprotein, beta polypeptide	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20230601	MGI			
1557710	Etfb	electron transferring flavoprotein, beta polypeptide	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1557710	Etfb	electron transferring flavoprotein, beta polypeptide	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20230601	MGI			
1557710	Etfb	electron transferring flavoprotein, beta polypeptide	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20240523	MGI			
1557710	Etfb	electron transferring flavoprotein, beta polypeptide	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1557712	Wdr38	WD repeat domain 38	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20241121	MGI			
1557712	Wdr38	WD repeat domain 38	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20250508	MGI			
1557712	Wdr38	WD repeat domain 38	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1557712	Wdr38	WD repeat domain 38	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20250508	MGI			
1557712	Wdr38	WD repeat domain 38	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20241121	MGI			
1557712	Wdr38	WD repeat domain 38	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20241121	MGI			
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20230119	MGI			
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0001765	abnormal ion homeostasis		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0002753	dilated heart left ventricle		IEA		N	RGD:5509061	20240523	MGI			
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20240523	MGI			
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20231026	MGI			PMID:37150501
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0011886	increased circulating lipase level		IEA		N	RGD:5509061	20260402	MGI			
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0020867	increased lipogenesis		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557713	Acot12	acyl-CoA thioesterase 12	gene	MP:0031265	increased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20250925	MGI			PMID:34285335
1557715	Tle6	transducin-like enhancer of split 6	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1557715	Tle6	transducin-like enhancer of split 6	gene	MP:0003406	failure of zygotic cell division		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1557715	Tle6	transducin-like enhancer of split 6	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1557715	Tle6	transducin-like enhancer of split 6	gene	MP:0020850	abnormal microtubule cytoskeleton morphology		IAGP		N	RGD:5509061	20200423	MGI			PMID:25208553
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7908720
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7908720
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555717
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7908720
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20151112	MGI			PMID:25283275
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18400903
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023301
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12023301
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7908720
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18400903
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0009322	increased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555717
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0009323	abnormal spleen development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7555717
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0009323	abnormal spleen development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7908720
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0010178	increased number of Howell-Jolly bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:7908720
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0011263	abnormal spleen mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7908720
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0021091	abnormal dorsal interneuron morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:12023301
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0021093	abnormal dorsal interneuron 2 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:12023301
1557716	Tlx1	T cell leukemia, homeobox 1	gene	MP:0021095	abnormal dorsal interneuron 4 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:12023301
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20240523	MGI			
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20260423	MGI			PMID:39244620
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20260423	MGI			PMID:39244620
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20260423	MGI			PMID:39244620
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20240523	MGI			
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20240229	MGI			PMID:38031972
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20260430	MGI			PMID:39277687
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20240229	MGI			PMID:38031972
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001893	non-obstructive hydrocephaly		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260423	MGI			PMID:39244620
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001947	abnormal mucociliary clearance		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20260430	MGI			PMID:39277687
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20260430	MGI			PMID:39277687
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0004302	abnormal Deiters cell morphology		IAGP		N	RGD:5509061	20260430	MGI			PMID:39277687
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20260423	MGI			PMID:39244620
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20260423	MGI			PMID:39244620
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20260423	MGI			PMID:39244620
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20240229	MGI			PMID:38031972
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:38031972
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240229	MGI			PMID:38031972
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0011644	abnormal oviduct epithelium motile cilium morphology		IAGP		N	RGD:5509061	20240229	MGI			PMID:38031972
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0011644	abnormal oviduct epithelium motile cilium morphology		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0013206	abnormal motile cilium morphology		IAGP		N	RGD:5509061	20260430	MGI			PMID:39277687
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0013206	abnormal motile cilium morphology		IAGP		N	RGD:5509061	20260514	MGI			PMID:38662826
1557719	Tubb4b	tubulin, beta 4B class IVB	gene	MP:0014409	decreased distortion product otoacoustic emission amplitude		IAGP		N	RGD:5509061	20260430	MGI			PMID:39277687
1557720	Cfp	complement factor properdin	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22308431
1557720	Cfp	complement factor properdin	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916747
1557720	Cfp	complement factor properdin	gene	MP:0002471	abnormal complement pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916747
1557720	Cfp	complement factor properdin	gene	MP:0002472	impaired complement alternative pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916747
1557720	Cfp	complement factor properdin	gene	MP:0002472	impaired complement alternative pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:20941861
1557720	Cfp	complement factor properdin	gene	MP:0002473	impaired complement classical pathway		IAGP		N	RGD:5509061	20141003	MGI			PMID:17916747
1557720	Cfp	complement factor properdin	gene	MP:0003436	decreased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20941861
1557720	Cfp	complement factor properdin	gene	MP:0005044	sepsis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292556
1557720	Cfp	complement factor properdin	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22308431
1557720	Cfp	complement factor properdin	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18292556
1557721	Pbrm1	polybromo 1	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601824
1557721	Pbrm1	polybromo 1	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601824
1557721	Pbrm1	polybromo 1	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601824
1557721	Pbrm1	polybromo 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1557721	Pbrm1	polybromo 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601824
1557721	Pbrm1	polybromo 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1557721	Pbrm1	polybromo 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20181227	MGI			
1557721	Pbrm1	polybromo 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601824
1557721	Pbrm1	polybromo 1	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601824
1557721	Pbrm1	polybromo 1	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601824
1557721	Pbrm1	polybromo 1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20161201	MGI			PMID:22336179
1557721	Pbrm1	polybromo 1	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20161201	MGI			PMID:22336179
1557721	Pbrm1	polybromo 1	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20161201	MGI			PMID:22336179
1557721	Pbrm1	polybromo 1	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20161201	MGI			PMID:22336179
1557721	Pbrm1	polybromo 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1557721	Pbrm1	polybromo 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601824
1557721	Pbrm1	polybromo 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557722	Galnt4	polypeptide N-acetylgalactosaminyltransferase 4	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557723	Sumo3	small ubiquitin-like modifier 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20151112	MGI			PMID:24891386
1557723	Sumo3	small ubiquitin-like modifier 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151112	MGI			PMID:24891386
1557723	Sumo3	small ubiquitin-like modifier 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20151112	MGI			PMID:24891386
1557723	Sumo3	small ubiquitin-like modifier 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20151112	MGI			PMID:24891386
1557724	Trim62	tripartite motif-containing 62	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557724	Trim62	tripartite motif-containing 62	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557724	Trim62	tripartite motif-containing 62	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557724	Trim62	tripartite motif-containing 62	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557724	Trim62	tripartite motif-containing 62	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557724	Trim62	tripartite motif-containing 62	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557724	Trim62	tripartite motif-containing 62	gene	MP:0009308	increased adenocarcinoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557724	Trim62	tripartite motif-containing 62	gene	MP:0009591	increased liver adenocarcinoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557724	Trim62	tripartite motif-containing 62	gene	MP:0010367	increased spindle cell carcinoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557724	Trim62	tripartite motif-containing 62	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141127	MGI			PMID:23838884
1557725	Itga2b	integrin alpha 2b	gene	MP:0000229	abnormal megakaryocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935982
1557725	Itga2b	integrin alpha 2b	gene	MP:0000440	domed cranium		IEA		N	RGD:5509061	20200604	MGI			
1557725	Itga2b	integrin alpha 2b	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871637
1557725	Itga2b	integrin alpha 2b	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20200604	MGI			
1557725	Itga2b	integrin alpha 2b	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20200604	MGI			
1557725	Itga2b	integrin alpha 2b	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871637
1557725	Itga2b	integrin alpha 2b	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935982
1557725	Itga2b	integrin alpha 2b	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871637
1557725	Itga2b	integrin alpha 2b	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17309829
1557725	Itga2b	integrin alpha 2b	gene	MP:0003396	abnormal embryonic hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871637
1557725	Itga2b	integrin alpha 2b	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871637
1557725	Itga2b	integrin alpha 2b	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871637
1557725	Itga2b	integrin alpha 2b	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17309829
1557725	Itga2b	integrin alpha 2b	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935982
1557725	Itga2b	integrin alpha 2b	gene	MP:0009548	abnormal platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0009676	abnormal hemostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20200604	MGI			
1557725	Itga2b	integrin alpha 2b	gene	MP:0011380	enlarged brain ventricles		IEA		N	RGD:5509061	20200604	MGI			
1557725	Itga2b	integrin alpha 2b	gene	MP:0014060	abnormal platelet alpha-granule morphology		IAGP		N	RGD:5509061	20170803	MGI			PMID:10942384
1557725	Itga2b	integrin alpha 2b	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:12871637
1557725	Itga2b	integrin alpha 2b	gene	MP:0031152	subcutaneous hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:10942384
1557726	Efhd1	EF hand domain containing 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1557726	Efhd1	EF hand domain containing 1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1557726	Efhd1	EF hand domain containing 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1557726	Efhd1	EF hand domain containing 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1557726	Efhd1	EF hand domain containing 1	gene	MP:0010055	abnormal sensory neuron physiology		IAGP		N	RGD:5509061	20210603	MGI			PMID:32414840
1557728	Tex11	testis expressed gene 11	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369460
1557728	Tex11	testis expressed gene 11	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316482
1557728	Tex11	testis expressed gene 11	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316482
1557728	Tex11	testis expressed gene 11	gene	MP:0004218	meiotic nondisjunction during M1 phase		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316482
1557728	Tex11	testis expressed gene 11	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316482
1557728	Tex11	testis expressed gene 11	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18369460
1557728	Tex11	testis expressed gene 11	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316482
1557728	Tex11	testis expressed gene 11	gene	MP:0008966	abnormal chiasmata formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18316482
1557728	Tex11	testis expressed gene 11	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:18316482
1557729	Map4	microtubule-associated protein 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20250313	MGI			PMID:39473976
1557729	Map4	microtubule-associated protein 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9626500
1557729	Map4	microtubule-associated protein 4	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20250313	MGI			PMID:39473976
1557729	Map4	microtubule-associated protein 4	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20250313	MGI			PMID:39473976
1557729	Map4	microtubule-associated protein 4	gene	MP:0005369	muscle phenotype		IAGP		N	RGD:5509061	20250313	MGI			PMID:39473976
1557729	Map4	microtubule-associated protein 4	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20250313	MGI			PMID:39473976
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0006062	abnormal vena cava morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0008933	abnormal motile primary cilium physiology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0010975	abnormal lung lobe morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0011649	immotile respiratory cilia		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0013858	abnormal azygos vein topology		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557730	Dnaaf11	dynein axonemal assembly factor 11	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20190418	MGI			PMID:27353389
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000542	left-sided isomerism		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000650	mesocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0003342	accessory spleen		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0004113	abnormal aortic arch morphology		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0004133	heterotaxia		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0006113	abnormal heart septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010412	atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010422	heart right ventricle hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010426	abnormal heart and great artery attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010443	total anomalous pulmonary venous connection, intracardiac		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010454	abnormal truncus arteriosus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010487	abnormal right subclavian artery morphology		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10574770
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0011254	superior-inferior ventricles		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0011569	abnormal azygos vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10521397
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0011665	d-loop transposition of the great arteries		IEA		N	RGD:5509061	20141003	MGI			
1557732	Cfc1	cryptic, EGF-CFC family member 1	gene	MP:0011673	unbalanced complete common atrioventricular canal		IEA		N	RGD:5509061	20210708	MGI			
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0008061	absent podocyte slit diaphragm		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0011856	abnormal glomerular filtration barrier function		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557733	Srgap1	SLIT-ROBO Rho GTPase activating protein 1	gene	MP:0011869	detached podocyte		IAGP		N	RGD:5509061	20230323	MGI			PMID:33514561
1557735	Stradb	STE20-related kinase adaptor beta	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1557735	Stradb	STE20-related kinase adaptor beta	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1557736	Pyy	peptide YY	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0000013	abnormal adipose tissue distribution		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950139
1557736	Pyy	peptide YY	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792209
1557736	Pyy	peptide YY	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920065
1557736	Pyy	peptide YY	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950139
1557736	Pyy	peptide YY	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950139
1557736	Pyy	peptide YY	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870288
1557736	Pyy	peptide YY	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950139
1557736	Pyy	peptide YY	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792209
1557736	Pyy	peptide YY	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920065
1557736	Pyy	peptide YY	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792209
1557736	Pyy	peptide YY	gene	MP:0003212	increased susceptibility to age related obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950139
1557736	Pyy	peptide YY	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792209
1557736	Pyy	peptide YY	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920065
1557736	Pyy	peptide YY	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920065
1557736	Pyy	peptide YY	gene	MP:0004702	increased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920065
1557736	Pyy	peptide YY	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920065
1557736	Pyy	peptide YY	gene	MP:0005645	abnormal hypothalamus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950139
1557736	Pyy	peptide YY	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16950139
1557736	Pyy	peptide YY	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16680491
1557736	Pyy	peptide YY	gene	MP:0010123	increased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792209
1557736	Pyy	peptide YY	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20141003	MGI			PMID:17920065
1557736	Pyy	peptide YY	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792209
1557736	Pyy	peptide YY	gene	MP:0021191	increased bone mineral density of lumbar vertebrae		IAGP		N	RGD:5509061	20220922	MGI			PMID:22792209
1557737	Tssk6	testis-specific serine kinase 6	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870294
1557737	Tssk6	testis-specific serine kinase 6	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870294
1557737	Tssk6	testis-specific serine kinase 6	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870294
1557737	Tssk6	testis-specific serine kinase 6	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870294
1557737	Tssk6	testis-specific serine kinase 6	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870294
1557740	Cd70	CD70 antigen	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269247
1557740	Cd70	CD70 antigen	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269247
1557740	Cd70	CD70 antigen	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269247
1557740	Cd70	CD70 antigen	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23547099
1557740	Cd70	CD70 antigen	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23269247
1557740	Cd70	CD70 antigen	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23269247
1557741	Herc6	hect domain and RLD 6	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1557741	Herc6	hect domain and RLD 6	gene	MP:0002997	enlarged seminal vesicle		IAGP		N	RGD:5509061	20221124	MGI			PMID:25406959
1557741	Herc6	hect domain and RLD 6	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1557741	Herc6	hect domain and RLD 6	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1557741	Herc6	hect domain and RLD 6	gene	MP:0013899	abnormal seminal vesicle epithelium morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:25406959
1557742	Phf14	PHD finger protein 14	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730381
1557742	Phf14	PHD finger protein 14	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1557742	Phf14	PHD finger protein 14	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210520	MGI			
1557742	Phf14	PHD finger protein 14	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20210520	MGI			
1557742	Phf14	PHD finger protein 14	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730381
1557742	Phf14	PHD finger protein 14	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730381
1557742	Phf14	PHD finger protein 14	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730381
1557742	Phf14	PHD finger protein 14	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20210520	MGI			
1557742	Phf14	PHD finger protein 14	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1557742	Phf14	PHD finger protein 14	gene	MP:0008277	abnormal sternum ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730381
1557742	Phf14	PHD finger protein 14	gene	MP:0010903	abnormal pulmonary alveolus wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730381
1557742	Phf14	PHD finger protein 14	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730381
1557742	Phf14	PHD finger protein 14	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210520	MGI			
1557742	Phf14	PHD finger protein 14	gene	MP:0011703	increased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22730381
1557744	Trim35	tripartite motif-containing 35	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1557744	Trim35	tripartite motif-containing 35	gene	MP:0008576	decreased circulating interferon-beta level		IAGP		N	RGD:5509061	20210408	MGI			PMID:32562145
1557744	Trim35	tripartite motif-containing 35	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210826	MGI			
1557744	Trim35	tripartite motif-containing 35	gene	MP:0011079	decreased macrophage cytokine production		IAGP		N	RGD:5509061	20210408	MGI			PMID:32562145
1557744	Trim35	tripartite motif-containing 35	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20210408	MGI			PMID:32562145
1557744	Trim35	tripartite motif-containing 35	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210408	MGI			PMID:32562145
1557746	Pde4c	phosphodiesterase 4C, cAMP specific	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1557746	Pde4c	phosphodiesterase 4C, cAMP specific	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1557746	Pde4c	phosphodiesterase 4C, cAMP specific	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20181227	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20160804	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20260402	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0002997	enlarged seminal vesicle		IEA		N	RGD:5509061	20201022	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0003959	abnormal lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0004142	abnormal muscle tone		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0004651	increased thoracic vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20201022	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0008181	increased marginal zone B cell number		IEA		N	RGD:5509061	20210520	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20201022	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0009401	increased skeletal muscle fiber diameter		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0009422	decreased gastrocnemius weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20201022	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20241121	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0010100	increased cervical vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0012107	enhanced exercise endurance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18846255
1557747	Myoz1	myozenin 1	gene	MP:0012320	abnormal body fat mass		IEA		N	RGD:5509061	20260402	MGI			
1557747	Myoz1	myozenin 1	gene	MP:0031318	enhanced skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:18846255
1557748	Tlr12	toll-like receptor 12	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15001781
1557748	Tlr12	toll-like receptor 12	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15001781
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000344	absent Cajal-Retzius cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101327
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20190912	MGI			PMID:31197172
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20200402	MGI			PMID:30093551
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426285
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178126
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20151126	MGI			PMID:24771530
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000778	abnormal nervous system tract morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8812118
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20260716	MGI			PMID:22266795
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000784	forebrain hypoplasia		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820705
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000785	telencephalon hypoplasia		IAGP		N	RGD:5509061	20190912	MGI			PMID:31197172
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820705
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:22705452
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15115821
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17828260
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18202285
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658188
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20150521	MGI			PMID:24857653
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000805	abnormal visual cortex morphology		IAGP		N	RGD:5509061	20180830	MGI			PMID:29809135
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15115821
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719109
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101327
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101327
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20200402	MGI			PMID:30093551
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000809	absent hippocampus		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24174665
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20161208	MGI			PMID:24614806
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820705
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000823	abnormal lateral ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141016	MGI			PMID:22705452
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000860	abnormal primary somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498788
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000860	abnormal primary somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17828260
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000860	abnormal primary somatosensory cortex morphology		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000862	absent barrels in primary somatosensory cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000862	absent barrels in primary somatosensory cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12498788
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16436615
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24930700
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922229
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956903
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956903
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001401	jumpy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24784230
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:24784230
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141218	MGI			PMID:24937429
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956903
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001408	stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956903
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20171221	MGI			PMID:28346493
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20171221	MGI			PMID:28346493
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524897
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15115821
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17956903
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001731	abnormal postnatal growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141016	MGI			PMID:22705452
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080609
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001909	reduced NMDA receptor mediated synaptic activity in barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922229
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24930700
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719109
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260521	MGI			PMID:41679675
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579678
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24930700
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10963597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12151506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170126	MGI			PMID:27693255
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141218	MGI			PMID:24937429
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11027526
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8812118
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141218	MGI			PMID:24937429
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719109
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002659	pituitary gland hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426285
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487195
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22678282
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:24623763
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18625319
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:17299771
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20180329	MGI			PMID:28076783
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080609
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080609
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101327
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20150521	MGI			PMID:24857653
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178126
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719109
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21185282
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20250904	MGI			PMID:40369080
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201022	MGI			
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426285
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003817	abnormal pituitary diverticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426285
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17828260
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524897
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719109
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004097	abnormal cerebellar cortex morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004164	abnormal neurohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426285
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004171	abnormal pallium development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004171	abnormal pallium development		IAGP		N	RGD:5509061	20200402	MGI			PMID:30093551
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579678
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101327
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004495	decreased synaptic glutamate release		IAGP		N	RGD:5509061	20141003	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:20080609
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658188
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101327
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20150521	MGI			PMID:24857653
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30093551
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719109
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0004998	decreased CNS synapse formation		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21321212
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0005267	abnormal olfactory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820705
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719109
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20170629	MGI			PMID:27939640
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0005655	increased aggression		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658188
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20161208	MGI			PMID:24614806
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20180329	MGI			PMID:28076783
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12890780
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23178126
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20151126	MGI			PMID:24771530
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20170601	MGI			PMID:26795843
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20210527	MGI			PMID:32202496
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20260716	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008030	abnormal Cajal-Retzius cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21185282
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008030	abnormal Cajal-Retzius cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487195
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008128	abnormal brain internal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24930700
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:33086056
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008222	decreased hippocampal commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18487195
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008226	decreased anterior commissure size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008262	abnormal hippocampus region morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008264	absent hippocampus CA1 region		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008266	absent hippocampus CA2 region		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008268	absent hippocampus CA3 region		IAGP		N	RGD:5509061	20141003	MGI			PMID:15219872
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20150521	MGI			PMID:24857653
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008328	increased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426285
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008367	absent pituitary intermediate lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426285
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008462	abnormal medium spiny neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15115821
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17901218
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19820705
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452199
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22101327
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922229
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008571	abnormal synaptic bouton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24174665
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661288
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16410414
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008934	absent choroid plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579678
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008946	abnormal neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20190912	MGI			PMID:31197172
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30093551
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0008949	increased Cajal-Retzius cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579678
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009324	absent hippocampal fimbria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20667915
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009358	environmentally induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20161013	MGI			PMID:25143599
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20171221	MGI			PMID:28346493
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009457	whorled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357712
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009463	abnormal pituitary infundibular stalk morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17426285
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009682	abnormal anterior corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22284184
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23658188
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20335472
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18579678
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19709628
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23643363
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:28346493
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24174665
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009946	abnormal olfactory bulb layer morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009954	abnormal mitral cell morphology		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22726441
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0010011	ectopic hippocampus pyramidal cells		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0010014	hippocampus pyramidal cell degeneration		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:20399730
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20141016	MGI			PMID:22705452
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23359422
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20150122	MGI			PMID:24448406
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18702697
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150108	MGI			PMID:24719109
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011150	abnormal hippocampus stratum oriens morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:29311744
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011396	abnormal sleep behavior		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011723	ectopic neuron		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011724	ectopic cortical neuron		IAGP		N	RGD:5509061	20141003	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011724	ectopic cortical neuron		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011827	impaired neuron differentiation		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20230928	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012203	abnormal neuronal stem cell morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012203	abnormal neuronal stem cell morphology		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012204	abnormal neuronal stem cell physiology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31112699
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20161013	MGI			PMID:25143599
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012349	increased susceptibility to induction of seizure by inducing agent		IAGP		N	RGD:5509061	20180830	MGI			PMID:7806216
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012448	abnormal primary motor cortex morphology		IAGP		N	RGD:5509061	20210107	MGI			PMID:31715135
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:15115821
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20200402	MGI			PMID:30093551
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0012683	absent telencephalon		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0013227	small brain ventricles		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20161013	MGI			PMID:26290337
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0014254	increased paired-pulse ratio		IAGP		N	RGD:5509061	20230706	MGI			PMID:23136427
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0014254	increased paired-pulse ratio		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0014372	decreased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240328	MGI			PMID:18524897
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0014379	decreased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0014379	decreased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0014744	abnormal hippocampal mossy fiber suprapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0015020	thin cerebral cortex layer		IAGP		N	RGD:5509061	20260716	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:24614806
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260716	MGI			PMID:35604347
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020067	increased neocortex size		IAGP		N	RGD:5509061	20150101	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20161103	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20200102	MGI			PMID:27618312
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20210211	MGI			PMID:33086056
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20250904	MGI			PMID:40369080
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020337	abnormal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020379	abnormal sucrose solution preference		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020388	decreased radial glial cell number		IAGP		N	RGD:5509061	20161117	MGI			PMID:21185282
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020388	decreased radial glial cell number		IAGP		N	RGD:5509061	20161117	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020388	decreased radial glial cell number		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020388	decreased radial glial cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30093551
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020389	increased radial glial cell number		IAGP		N	RGD:5509061	20161117	MGI			PMID:25100583
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020389	increased radial glial cell number		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020391	radial glial endfoot detachment		IAGP		N	RGD:5509061	20161117	MGI			PMID:21185282
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020392	abnormal radial glial cell apoptosis		IAGP		N	RGD:5509061	20161117	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20161117	MGI			PMID:25948253
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20161117	MGI			PMID:21185282
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20170518	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20170629	MGI			PMID:25568313
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20241212	MGI			PMID:38306425
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20220721	MGI			PMID:35314861
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:14687546
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020536	increased subiculum size		IAGP		N	RGD:5509061	20180301	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020576	decreased corpus callosum cell number		IAGP		N	RGD:5509061	20260716	MGI			PMID:22266795
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020594	decreased cerebral cortex cell number		IAGP		N	RGD:5509061	20190215	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020594	decreased cerebral cortex cell number		IAGP		N	RGD:5509061	20260716	MGI			PMID:22266795
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0020912	abnormal susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20210211	MGI			PMID:33086056
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0021088	impaired spatial memory extinction		IAGP		N	RGD:5509061	20250417	MGI			PMID:38561334
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20250424	MGI			PMID:39779369
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0030004	hippocampus hypoplasia		IAGP		N	RGD:5509061	20170706	MGI			PMID:22266795
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0030707	decreased glutamine level		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0030733	decreased gamma-aminobutyric acid level		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0030737	decreased glutamic acid level		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0030743	decreased aspartic acid level		IAGP		N	RGD:5509061	20190418	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0030955	abnormal Golgi trans cisterna morphology		IAGP		N	RGD:5509061	20190725	MGI			PMID:24174665
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0030956	abnormal neuronal precursor cell migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:25757017
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:28288114
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:30053506
1557750	Emx1	empty spiracles homeobox 1	gene	MP:0031392	hypoactivity		IAGP		N	RGD:5509061	20220421	MGI			PMID:26868444
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016100
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016100
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0001739	abnormal adrenal gland secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19667187
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0001905	abnormal dopamine level		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828077
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150806	MGI			PMID:24427314
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20064389
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828077
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828077
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23270607
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20064389
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20190124	MGI			PMID:27383589
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828077
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20064389
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20064389
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:19667187
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850369
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0003858	enhanced coordination		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828077
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20064389
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20211125	MGI			PMID:34658337
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20211125	MGI			PMID:34658337
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0004153	increased renal tubule apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0004250	tau protein deposits		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828077
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0004980	increased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23270607
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0005060	accumulation of giant lysosomes in kidney/renal tubule cells		IAGP		N	RGD:5509061	20240718	MGI			PMID:32375042
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19667187
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19890007
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0006037	abnormal mitochondrial fission		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828077
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23270607
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19890007
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850369
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0008546	abnormal vesicle-mediated transport		IAGP		N	RGD:5509061	20240718	MGI			PMID:32375042
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21828077
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19667187
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20064389
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:19667187
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19667187
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20190124	MGI			PMID:27383589
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0010149	abnormal synaptic dopamine release		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20016100
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0011267	abnormal excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240418	MGI			PMID:27383589
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0011369	increased renal glomerulus apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0011534	granular kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20457918
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0011629	decreased mitochondrial number		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20160317	MGI			PMID:25836420
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20240418	MGI			PMID:27383589
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0030949	abnormal Golgi vesicle transport		IAGP		N	RGD:5509061	20240718	MGI			PMID:32375042
1557751	Lrrk2	leucine-rich repeat kinase 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:25836420
1557752	Fabp12	fatty acid binding protein 12	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1557755	Ndufaf2	NADH:ubiquinone oxidoreductase complex assembly factor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151119	MGI			PMID:23702311
1557755	Ndufaf2	NADH:ubiquinone oxidoreductase complex assembly factor 2	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:23702311
1557757	Spmap2l	sperm microtubule associated protein 2 like	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20231207	MGI			
1557757	Spmap2l	sperm microtubule associated protein 2 like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1557757	Spmap2l	sperm microtubule associated protein 2 like	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20250508	MGI			
1557757	Spmap2l	sperm microtubule associated protein 2 like	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20231207	MGI			
1557758	Pot1a	protection of telomeres 1A	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
1557758	Pot1a	protection of telomeres 1A	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0002393	abnormal bronchus-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0003155	abnormal telomere length		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
1557758	Pot1a	protection of telomeres 1A	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
1557758	Pot1a	protection of telomeres 1A	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
1557758	Pot1a	protection of telomeres 1A	gene	MP:0004028	chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
1557758	Pot1a	protection of telomeres 1A	gene	MP:0004964	absent inner cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839877
1557758	Pot1a	protection of telomeres 1A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839876
1557758	Pot1a	protection of telomeres 1A	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839877
1557758	Pot1a	protection of telomeres 1A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16839877
1557758	Pot1a	protection of telomeres 1A	gene	MP:0011416	abnormal testis interstitial tissue morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0014082	decreased small intestinal villus height		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0014241	abnormal intracellular organelle physiology		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557758	Pot1a	protection of telomeres 1A	gene	MP:0030927	decreased telomere length		IAGP		N	RGD:5509061	20260625	MGI			PMID:40954016
1557759	Ube2l3	ubiquitin-conjugating enzyme E2L 3	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901595
1557759	Ube2l3	ubiquitin-conjugating enzyme E2L 3	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901595
1557759	Ube2l3	ubiquitin-conjugating enzyme E2L 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901595
1557759	Ube2l3	ubiquitin-conjugating enzyme E2L 3	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901595
1557759	Ube2l3	ubiquitin-conjugating enzyme E2L 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901595
1557759	Ube2l3	ubiquitin-conjugating enzyme E2L 3	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8901595
1557760	Vps9d1	VPS9 domain containing 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1557760	Vps9d1	VPS9 domain containing 1	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20241121	MGI			
1557760	Vps9d1	VPS9 domain containing 1	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:31487266
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20200310	MGI			
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0003025	increased vasoconstriction		IAGP		N	RGD:5509061	20200310	MGI			PMID:31487266
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20200310	MGI			PMID:31487266
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:31487266
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0005590	increased vasodilation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31487266
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31487266
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20200310	MGI			PMID:31487266
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0012045	increased susceptibility to hypertension		IAGP		N	RGD:5509061	20200310	MGI			PMID:31487266
1557763	Cyb5r3	cytochrome b5 reductase 3	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1557764	Mthfs	5, 10-methenyltetrahydrofolate synthetase	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22303332
1557764	Mthfs	5, 10-methenyltetrahydrofolate synthetase	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22303332
1557764	Mthfs	5, 10-methenyltetrahydrofolate synthetase	gene	MP:0011230	abnormal folic acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22303332
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:17488636
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0002667	decreased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17488636
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003020	decreased circulating chloride level		IAGP		N	RGD:5509061	20181115	MGI			PMID:24655003
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003028	alkalosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003029	alkalemia		IAGP		N	RGD:5509061	20181115	MGI			PMID:24655003
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17488636
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0003860	abnormal carbon dioxide level		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0004119	hypokalemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0005502	abnormal renal/urinary system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17488636
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633012
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17488636
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0005634	decreased circulating sodium level		IAGP		N	RGD:5509061	20181115	MGI			PMID:24655003
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633012
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20181115	MGI			PMID:24655003
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0006274	abnormal urine sodium level		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19633012
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0010093	decreased circulating magnesium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22550170
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0012339	hyperkalemia		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557765	Wnk4	WNK lysine deficient protein kinase 4	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20200521	MGI			PMID:30765526
1557766	Gdpd2	glycerophosphodiester phosphodiesterase domain containing 2	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:31932351
1557766	Gdpd2	glycerophosphodiester phosphodiesterase domain containing 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20201231	MGI			PMID:31932351
1557766	Gdpd2	glycerophosphodiester phosphodiesterase domain containing 2	gene	MP:0010160	increased oligodendrocyte number		IAGP		N	RGD:5509061	20201231	MGI			PMID:31932351
1557766	Gdpd2	glycerophosphodiester phosphodiesterase domain containing 2	gene	MP:0010892	increased oligodendrocyte progenitor number		IAGP		N	RGD:5509061	20201231	MGI			PMID:31932351
1557766	Gdpd2	glycerophosphodiester phosphodiesterase domain containing 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1557766	Gdpd2	glycerophosphodiester phosphodiesterase domain containing 2	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20201231	MGI			PMID:31932351
1557767	Myo7b	myosin VIIB	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1557767	Myo7b	myosin VIIB	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1557767	Myo7b	myosin VIIB	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20160421	MGI			
1557769	Mepce	methylphosphate capping enzyme	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1557769	Mepce	methylphosphate capping enzyme	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1557769	Mepce	methylphosphate capping enzyme	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557769	Mepce	methylphosphate capping enzyme	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557770	Camp	cathelicidin antimicrobial peptide	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23670560
1557770	Camp	cathelicidin antimicrobial peptide	gene	MP:0001313	increased incidence of corneal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23670560
1557770	Camp	cathelicidin antimicrobial peptide	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11719807
1557770	Camp	cathelicidin antimicrobial peptide	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751768
1557770	Camp	cathelicidin antimicrobial peptide	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23670560
1557770	Camp	cathelicidin antimicrobial peptide	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23603910
1557770	Camp	cathelicidin antimicrobial peptide	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751768
1557770	Camp	cathelicidin antimicrobial peptide	gene	MP:0011518	abnormal cell chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23603910
1557771	Stk24	serine/threonine kinase 24	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20180614	MGI			PMID:24176643
1557771	Stk24	serine/threonine kinase 24	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20180614	MGI			PMID:24176643
1557771	Stk24	serine/threonine kinase 24	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20180614	MGI			PMID:24176643
1557771	Stk24	serine/threonine kinase 24	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20180614	MGI			PMID:24176643
1557771	Stk24	serine/threonine kinase 24	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1557772	Irs4	insulin receptor substrate 4	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10644546
1557772	Irs4	insulin receptor substrate 4	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10644546
1557772	Irs4	insulin receptor substrate 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10644546
1557772	Irs4	insulin receptor substrate 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
1557772	Irs4	insulin receptor substrate 4	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10644546
1557772	Irs4	insulin receptor substrate 4	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
1557772	Irs4	insulin receptor substrate 4	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:10644546
1557772	Irs4	insulin receptor substrate 4	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005291	abnormal glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10644546
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10644546
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12502742
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005452	abnormal adipose tissue amount		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10644546
1557772	Irs4	insulin receptor substrate 4	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0009124	increased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557772	Irs4	insulin receptor substrate 4	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20160204	MGI			PMID:24567904
1557773	Pnma3	paraneoplastic antigen MA3	gene	MP:0008820	abnormal blood uric acid level		IEA		N	RGD:5509061	20210520	MGI			
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19632227
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19632227
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19632227
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19632227
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19632227
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19632227
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19632227
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19632227
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23487419
1557774	Clec4g	C-type lectin domain family 4, member g	gene	MP:0020932	decreased susceptibility to Adenoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:23487419
1557775	Cdc45	cell division cycle 45	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416137
1557775	Cdc45	cell division cycle 45	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416137
1557775	Cdc45	cell division cycle 45	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557775	Cdc45	cell division cycle 45	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416137
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250220	MGI			PMID:39827215
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20250220	MGI			PMID:39827215
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20250220	MGI			PMID:39827215
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20250220	MGI			PMID:39827215
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20250220	MGI			PMID:39827215
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20250220	MGI			PMID:39827215
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20211021	MGI			
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:39827215
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20250220	MGI			PMID:39827215
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20250220	MGI			PMID:39827215
1557776	Dynlt2b	dynein light chain Tctex-type 2B	gene	MP:0031356	abnormal outer dense fiber morphology		IAGP		N	RGD:5509061	20250220	MGI			PMID:39827215
1557777	Dock11	dedicator of cytokinesis 11	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1557777	Dock11	dedicator of cytokinesis 11	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:25729399
1557777	Dock11	dedicator of cytokinesis 11	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20220908	MGI			PMID:32241915
1557777	Dock11	dedicator of cytokinesis 11	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20211021	MGI			
1557777	Dock11	dedicator of cytokinesis 11	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20210429	MGI			PMID:25729399
1557777	Dock11	dedicator of cytokinesis 11	gene	MP:0008241	abnormal metallophilic macrophage morphology		IAGP		N	RGD:5509061	20210429	MGI			PMID:25729399
1557777	Dock11	dedicator of cytokinesis 11	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20210429	MGI			PMID:25729399
1557778	Pam16	presequence translocase-asssociated motor 16	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557778	Pam16	presequence translocase-asssociated motor 16	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557778	Pam16	presequence translocase-asssociated motor 16	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1557779	Tceal3	transcription elongation factor A (SII)-like 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1557779	Tceal3	transcription elongation factor A (SII)-like 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1557779	Tceal3	transcription elongation factor A (SII)-like 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20181227	MGI			
1557780	Clec9a	C-type lectin domain family 9, member a	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22209163
1557780	Clec9a	C-type lectin domain family 9, member a	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19219027
1557780	Clec9a	C-type lectin domain family 9, member a	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20211021	MGI			
1557781	Fkbp9	FK506 binding protein 9	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20260514	MGI			PMID:39281835
1557781	Fkbp9	FK506 binding protein 9	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1557781	Fkbp9	FK506 binding protein 9	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1557781	Fkbp9	FK506 binding protein 9	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20160804	MGI			
1557781	Fkbp9	FK506 binding protein 9	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20160804	MGI			
1557781	Fkbp9	FK506 binding protein 9	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20260514	MGI			PMID:39281835
1557781	Fkbp9	FK506 binding protein 9	gene	MP:0014756	decreased tumor cell proliferation		IAGP		N	RGD:5509061	20260514	MGI			PMID:39281835
1557781	Fkbp9	FK506 binding protein 9	gene	MP:0014757	increased tumor cell death		IAGP		N	RGD:5509061	20260514	MGI			PMID:39281835
1557783	En2	engrailed 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7909289
1557783	En2	engrailed 2	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12832534
1557783	En2	engrailed 2	gene	MP:0000850	absent cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:1672471
1557783	En2	engrailed 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:7909289
1557783	En2	engrailed 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8652061
1557783	En2	engrailed 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:1672471
1557783	En2	engrailed 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7909289
1557783	En2	engrailed 2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1672471
1557783	En2	engrailed 2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7909289
1557783	En2	engrailed 2	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8652061
1557783	En2	engrailed 2	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1672471
1557783	En2	engrailed 2	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000865	absent cerebellum vermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0000866	cerebellum vermis hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000867	abnormal cerebellum anterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0000868	decreased anterior vermis size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000869	abnormal cerebellum posterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0000869	abnormal cerebellum posterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000869	abnormal cerebellum posterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7909289
1557783	En2	engrailed 2	gene	MP:0000869	abnormal cerebellum posterior vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8652061
1557783	En2	engrailed 2	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:7909289
1557783	En2	engrailed 2	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7909289
1557783	En2	engrailed 2	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0000900	decreased colliculi size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7909289
1557783	En2	engrailed 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8652061
1557783	En2	engrailed 2	gene	MP:0001440	abnormal grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001515	abnormal grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0002892	decreased superior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8652061
1557783	En2	engrailed 2	gene	MP:0003863	decreased aggression towards mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0003867	increased defecation amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:8652061
1557783	En2	engrailed 2	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0004096	abnormal midbrain-hindbrain boundary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124114
1557783	En2	engrailed 2	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:8652061
1557783	En2	engrailed 2	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0006105	small tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0006106	absent tectum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0009038	decreased inferior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0009039	absent inferior colliculus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0009040	absent superior colliculus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0009041	absent colliculi		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0009957	abnormal cerebellum vermis lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0009963	abnormal cerebellum hemisphere lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0009968	abnormal cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:16935268
1557783	En2	engrailed 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20081196
1557783	En2	engrailed 2	gene	MP:0011448	decreased dopaminergic neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015829
1557783	En2	engrailed 2	gene	MP:0012087	absent midbrain		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124114
1557783	En2	engrailed 2	gene	MP:0012089	decreased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0012133	absent midbrain-hindbrain boundary		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124114
1557783	En2	engrailed 2	gene	MP:0012785	decreased rhombomere 1 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124114
1557783	En2	engrailed 2	gene	MP:0012785	decreased rhombomere 1 size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17537797
1557783	En2	engrailed 2	gene	MP:0012787	absent rhombomere 1		IAGP		N	RGD:5509061	20141003	MGI			PMID:11124114
1557784	Kcp	kielin/chordin-like protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557784	Kcp	kielin/chordin-like protein	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557784	Kcp	kielin/chordin-like protein	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793581
1557784	Kcp	kielin/chordin-like protein	gene	MP:0003639	abnormal response to vitamins		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793581
1557784	Kcp	kielin/chordin-like protein	gene	MP:0004505	decreased renal glomerulus number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557784	Kcp	kielin/chordin-like protein	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557784	Kcp	kielin/chordin-like protein	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15793581
1557784	Kcp	kielin/chordin-like protein	gene	MP:0011376	abnormal kidney corticomedullary boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035289
1557785	Asb5	ankyrin repeat and SOCs box-containing 5	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20201231	MGI			
1557785	Asb5	ankyrin repeat and SOCs box-containing 5	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20200514	MGI			
1557785	Asb5	ankyrin repeat and SOCs box-containing 5	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20200514	MGI			
1557785	Asb5	ankyrin repeat and SOCs box-containing 5	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20260402	MGI			
1557785	Asb5	ankyrin repeat and SOCs box-containing 5	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20201022	MGI			
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20210506	MGI			PMID:27504012
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20210506	MGI			PMID:27504012
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20210506	MGI			PMID:27504012
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0004993	decreased bone resorption		IAGP		N	RGD:5509061	20190620	MGI			PMID:30550785
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20210506	MGI			PMID:27504012
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20210506	MGI			PMID:30940158
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0008753	abnormal osteocyte morphology		IAGP		N	RGD:5509061	20190620	MGI			PMID:30550785
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20210506	MGI			PMID:30940158
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20190620	MGI			PMID:30550785
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0010932	increased trabecular bone connectivity density		IAGP		N	RGD:5509061	20190620	MGI			PMID:30550785
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0010953	abnormal fatty acid oxidation		IAGP		N	RGD:5509061	20210506	MGI			PMID:27504012
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0012072	decreased susceptibility to osteoporosis		IAGP		N	RGD:5509061	20190620	MGI			PMID:30550785
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0030484	abnormal osteocyte lacuna morphology		IAGP		N	RGD:5509061	20190620	MGI			PMID:30550785
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20210610	MGI			PMID:27504012
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0031265	increased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:27504012
1557788	Fndc5	fibronectin type III domain containing 5	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:27504012
1557790	Nkap	NFKB activating protein	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409814
1557790	Nkap	NFKB activating protein	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409814
1557790	Nkap	NFKB activating protein	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409814
1557790	Nkap	NFKB activating protein	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409814
1557790	Nkap	NFKB activating protein	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409814
1557790	Nkap	NFKB activating protein	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409814
1557790	Nkap	NFKB activating protein	gene	MP:0010133	increased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409814
1557790	Nkap	NFKB activating protein	gene	MP:0010136	decreased DN4 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19409814
1557791	Lonrf3	LON peptidase N-terminal domain and ring finger 3	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1557791	Lonrf3	LON peptidase N-terminal domain and ring finger 3	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20210128	MGI			
1557791	Lonrf3	LON peptidase N-terminal domain and ring finger 3	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20210128	MGI			
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0002217	small lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23603910
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107188
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107188
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107188
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0004842	abnormal large intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0005087	decreased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107188
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:20107188
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23603910
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008720	impaired neutrophil chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23454745
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0010740	abnormal dendritic cell chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23603910
1557793	Fpr2	formyl peptide receptor 2	gene	MP:0010862	decreased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20200280
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530751
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001056	abnormal cranial nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530751
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001061	abnormal oculomotor nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530751
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001063	abnormal trochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530751
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20250508	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20250508	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164181
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23762465
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001689	incomplete somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23762465
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001700	abnormal embryo turning		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23762465
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002824	abnormal chorioallantoic fusion		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002861	abnormal tail bud morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0002884	abnormal pharyngeal arch morphology		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0004556	enlarged allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0005181	decreased circulating estradiol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20161201	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0008786	abnormal hindgut morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0009010	abnormal diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0009433	polyovular ovarian follicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12912906
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0009768	impaired somite development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23762465
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19164181
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23762465
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0012086	absent hindgut		IAGP		N	RGD:5509061	20141003	MGI			PMID:12381721
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0012544	abnormal caudal neuropore morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11134352
1557794	Nr6a1	nuclear receptor subfamily 6, group A, member 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557795	Zfp277	zinc finger protein 277	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20808772
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570919
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20190912	MGI			PMID:28129027
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:28129027
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:24305829
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570919
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003727	abnormal retina layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:24305829
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003881	abnormal nephron morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0004754	abnormal kidney collecting duct morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0004857	abnormal heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570919
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005419	decreased circulating serum albumin level		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:20570919
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0006376	decreased circulating angiotensinogen level		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20190912	MGI			PMID:24305829
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0009349	increased urine pH		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0009640	abnormal renal tubule epithelium morphology		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0010080	abnormal hepatocyte physiology		IAGP		N	RGD:5509061	20190912	MGI			PMID:28129027
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20570919
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011282	increased podocyte apoptosis		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011334	abnormal nephrogenic zone morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011351	absent proximal convoluted tubule brush border		IAGP		N	RGD:5509061	20160721	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011402	renal cast		IAGP		N	RGD:5509061	20160915	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011457	abnormal metanephric ureteric bud development		IAGP		N	RGD:5509061	20190912	MGI			PMID:23704941
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011951	increased cardiac stroke volume		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20190912	MGI			PMID:24305829
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0012024	abnormal nephron morphogenesis		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0012025	abnormal comma shaped body morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0012026	abnormal S-shaped body morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26658320
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0012046	decreased susceptibility to hypertension		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20190912	MGI			PMID:24305829
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20190912	MGI			PMID:24305829
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0020378	abnormal cell cytoskeleton morphology		IAGP		N	RGD:5509061	20161013	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:22034640
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20190912	MGI			PMID:28129027
1557796	Atp6ap2	ATPase, H+ transporting, lysosomal accessory protein 2	gene	MP:0031358	decreased urine output		IAGP		N	RGD:5509061	20230629	MGI			PMID:33890822
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314041
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0003131	increased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314041
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17526724
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15833813
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15833813
1557797	Bcl6b	B cell CLL/lymphoma 6, member B	gene	MP:0008050	decreased memory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15833813
1557798	Treml1	triggering receptor expressed on myeloid cells-like 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436112
1557798	Treml1	triggering receptor expressed on myeloid cells-like 1	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436112
1557798	Treml1	triggering receptor expressed on myeloid cells-like 1	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436112
1557798	Treml1	triggering receptor expressed on myeloid cells-like 1	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436112
1557798	Treml1	triggering receptor expressed on myeloid cells-like 1	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436112
1557798	Treml1	triggering receptor expressed on myeloid cells-like 1	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436112
1557798	Treml1	triggering receptor expressed on myeloid cells-like 1	gene	MP:0011514	skin hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19436112
1557798	Treml1	triggering receptor expressed on myeloid cells-like 1	gene	MP:0031083	increased circulating D-dimer level		IAGP		N	RGD:5509061	20200709	MGI			PMID:19436112
1557802	Ldb3	LIM domain binding 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20250508	MGI			
1557802	Ldb3	LIM domain binding 3	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12499364
1557802	Ldb3	LIM domain binding 3	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12499364
1557802	Ldb3	LIM domain binding 3	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20200402	MGI			
1557802	Ldb3	LIM domain binding 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12499364
1557802	Ldb3	LIM domain binding 3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1557802	Ldb3	LIM domain binding 3	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1557802	Ldb3	LIM domain binding 3	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20200402	MGI			
1557802	Ldb3	LIM domain binding 3	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12499364
1557802	Ldb3	LIM domain binding 3	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0003158	dysphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20231109	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12499364
1557802	Ldb3	LIM domain binding 3	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12499364
1557802	Ldb3	LIM domain binding 3	gene	MP:0010021	heart vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20210128	MGI			
1557802	Ldb3	LIM domain binding 3	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0010563	increased heart right ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19028670
1557802	Ldb3	LIM domain binding 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12499364
1557802	Ldb3	LIM domain binding 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11696561
1557802	Ldb3	LIM domain binding 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557802	Ldb3	LIM domain binding 3	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1557802	Ldb3	LIM domain binding 3	gene	MP:0014316	decreased heart left ventricle posterior wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:21303826
1557802	Ldb3	LIM domain binding 3	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:19028670
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210128	MGI			
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0001680	abnormal mesoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0001705	abnormal proximal-distal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0005157	holoprosencephaly		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0005163	cyclopia		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0006290	proboscis		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0011192	decreased embryonic epiblast cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0011259	abnormal cephalic neural fold morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0012685	abnormal primitive streak elongation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20040491
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557804	Tgif2	TGFB-induced factor homeobox 2	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20160929	MGI			PMID:22383895
1557806	Trnt1	tRNA nucleotidyl transferase, CCA-adding, 1	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1557806	Trnt1	tRNA nucleotidyl transferase, CCA-adding, 1	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20160804	MGI			
1557806	Trnt1	tRNA nucleotidyl transferase, CCA-adding, 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1557807	Plxna1	plexin A1	gene	MP:0000953	abnormal oligodendrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145500
1557807	Plxna1	plexin A1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1557807	Plxna1	plexin A1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715077
1557807	Plxna1	plexin A1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20512151
1557807	Plxna1	plexin A1	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715077
1557807	Plxna1	plexin A1	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1557807	Plxna1	plexin A1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1557807	Plxna1	plexin A1	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1557807	Plxna1	plexin A1	gene	MP:0004297	abnormal proprioceptive neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17145500
1557807	Plxna1	plexin A1	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20512151
1557807	Plxna1	plexin A1	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1557807	Plxna1	plexin A1	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715077
1557807	Plxna1	plexin A1	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1557807	Plxna1	plexin A1	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1557807	Plxna1	plexin A1	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1557807	Plxna1	plexin A1	gene	MP:0010197	abnormal lymphatic vessel endothelial cell morphology		IAGP		N	RGD:5509061	20170525	MGI			PMID:26319580
1557807	Plxna1	plexin A1	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16715077
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20191219	MGI			PMID:30613052
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0004559	small allantois		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0004760	increased mitotic index		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20230629	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0011257	abnormal head fold morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0012099	decreased spongiotrophoblast size		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0012504	increased forebrain apoptosis		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IAGP		N	RGD:5509061	20191219	MGI			PMID:30613052
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20160616	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0014259	embryonic lethality prior to organogenesis, complete penetrance		IAGP		N	RGD:5509061	20230706	MGI			PMID:27179789
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0020389	increased radial glial cell number		IAGP		N	RGD:5509061	20260625	MGI			PMID:41312597
1557808	Ddx3x	DEAD box helicase 3, X-linked	gene	MP:0030989	decreased spongiotrophoblast cell number		IAGP		N	RGD:5509061	20191219	MGI			PMID:27179789
1557809	Ero1b	endoplasmic reticulum oxidoreductase 1 beta	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
1557809	Ero1b	endoplasmic reticulum oxidoreductase 1 beta	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
1557809	Ero1b	endoplasmic reticulum oxidoreductase 1 beta	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
1557809	Ero1b	endoplasmic reticulum oxidoreductase 1 beta	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
1557809	Ero1b	endoplasmic reticulum oxidoreductase 1 beta	gene	MP:0009172	small pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
1557809	Ero1b	endoplasmic reticulum oxidoreductase 1 beta	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:20308425
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20180125	MGI			PMID:28827407
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:28827407
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0004264	abnormal extraembryonic tissue physiology		IAGP		N	RGD:5509061	20180125	MGI			PMID:28827407
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20201022	MGI			
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20180125	MGI			PMID:28827407
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0008932	abnormal embryonic tissue physiology		IAGP		N	RGD:5509061	20180125	MGI			PMID:28827407
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180125	MGI			PMID:28827407
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20170105	MGI			
1557811	Arl8b	ADP-ribosylation factor-like 8B	gene	MP:0020515	abnormal visceral yolk sac endoderm morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:28827407
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0001214	skin hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0003667	increased hemangiosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0009321	increased histiocytic sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0010344	increased hibernoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0013538	increased Harderian gland adenoma incidence		IAGP		N	RGD:5509061	20150219	MGI			PMID:21436583
1557812	Pinx1	PIN2/TERF1 interacting, telomerase inhibitor 1	gene	MP:0030928	increased telomere length		IAGP		N	RGD:5509061	20190117	MGI			PMID:21436583
1557813	Edem1	ER degradation enhancer, mannosidase alpha-like 1	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20241121	MGI			
1557813	Edem1	ER degradation enhancer, mannosidase alpha-like 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1557813	Edem1	ER degradation enhancer, mannosidase alpha-like 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20230601	MGI			
1557813	Edem1	ER degradation enhancer, mannosidase alpha-like 1	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20260402	MGI			
1557813	Edem1	ER degradation enhancer, mannosidase alpha-like 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1557813	Edem1	ER degradation enhancer, mannosidase alpha-like 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1557813	Edem1	ER degradation enhancer, mannosidase alpha-like 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1557815	Nbas	neuroblastoma amplified sequence	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20201231	MGI			
1557815	Nbas	neuroblastoma amplified sequence	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1557815	Nbas	neuroblastoma amplified sequence	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1557815	Nbas	neuroblastoma amplified sequence	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20181227	MGI			
1557815	Nbas	neuroblastoma amplified sequence	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20181227	MGI			
1557815	Nbas	neuroblastoma amplified sequence	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20211021	MGI			
1557815	Nbas	neuroblastoma amplified sequence	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1557815	Nbas	neuroblastoma amplified sequence	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0002908	delayed wound healing		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20111116	MGI			
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0005369	muscle phenotype		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0005376	homeostasis/metabolism phenotype		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0005378	growth/size/body region phenotype		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0005380	embryo phenotype		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0005385	cardiovascular system phenotype		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0005386	behavior/neurological phenotype		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0010954	abnormal cellular respiration		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557816	Npl	N-acetylneuraminate pyruvate lyase	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20240104	MGI			PMID:37390204
1557817	Mr1	major histocompatibility complex, class I-related	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20230119	MGI			
1557817	Mr1	major histocompatibility complex, class I-related	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12634786
1557817	Mr1	major histocompatibility complex, class I-related	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16878136
1557817	Mr1	major histocompatibility complex, class I-related	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20230119	MGI			
1557817	Mr1	major histocompatibility complex, class I-related	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12634786
1557817	Mr1	major histocompatibility complex, class I-related	gene	MP:0020186	abnormal susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200416	MGI			PMID:31113973
1557821	Zftraf1	zinc finger TRAF type containing 1	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1557821	Zftraf1	zinc finger TRAF type containing 1	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1557821	Zftraf1	zinc finger TRAF type containing 1	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20230601	MGI			
1557822	Slco6d1	solute carrier organic anion transporter family, member 6d1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210128	MGI			
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0001460	abnormal olfactory discrimination memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481456
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18043734
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11481456
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20150611	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0030590	abnormal sperm fibrous sheath morphology		IAGP		N	RGD:5509061	20180621	MGI			PMID:11585928
1557823	Neurl1a	neuralized E3 ubiquitin protein ligase 1A	gene	MP:0031410	biflagellated sperm		IAGP		N	RGD:5509061	20220630	MGI			PMID:11585928
1557825	Slc52a2	solute carrier protein 52, member 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1557825	Slc52a2	solute carrier protein 52, member 2	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20160421	MGI			
1557825	Slc52a2	solute carrier protein 52, member 2	gene	MP:0002768	small adrenal glands		IEA		N	RGD:5509061	20160811	MGI			
1557825	Slc52a2	solute carrier protein 52, member 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1557825	Slc52a2	solute carrier protein 52, member 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20211028	MGI			PMID:33518683
1557825	Slc52a2	solute carrier protein 52, member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1557826	Sms	spermine synthase	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557826	Sms	spermine synthase	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557826	Sms	spermine synthase	gene	MP:0000162	lordosis		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557826	Sms	spermine synthase	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557826	Sms	spermine synthase	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557826	Sms	spermine synthase	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1557826	Sms	spermine synthase	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1557826	Sms	spermine synthase	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20160804	MGI			
1557826	Sms	spermine synthase	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20160804	MGI			
1557826	Sms	spermine synthase	gene	MP:0008039	increased NK T cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0008044	increased NK cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557826	Sms	spermine synthase	gene	MP:0013600	testis degeneration		IAGP		N	RGD:5509061	20160922	MGI			PMID:24652767
1557827	Ano7	anoctamin 7	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20181227	MGI			
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0000929	open neural tube		IEA		N	RGD:5509061	20111116	MGI			
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20141003	MGI			
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22699621
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22699621
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0003752	increased oral papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22699621
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0004180	failure of initiation of embryo turning		IEA		N	RGD:5509061	20111116	MGI			
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0004251	failure of heart looping		IEA		N	RGD:5509061	20111116	MGI			
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0009152	increased pancreatic intraepithelial neoplasia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22699621
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22699621
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0009657	failure of chorioallantoic fusion		IEA		N	RGD:5509061	20111116	MGI			
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0012105	delayed gastrulation		IEA		N	RGD:5509061	20141003	MGI			
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220630	MGI			PMID:28559472
1557828	Usp9x	ubiquitin specific peptidase 9, X chromosome	gene	MP:0014685	spermiation failure		IAGP		N	RGD:5509061	20250703	MGI			PMID:28559472
1557829	Pmm2	phosphomannomutase 2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1557829	Pmm2	phosphomannomutase 2	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847317
1557829	Pmm2	phosphomannomutase 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0004144	hypotonia		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210128	MGI			
1557829	Pmm2	phosphomannomutase 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16847317
1557829	Pmm2	phosphomannomutase 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1557829	Pmm2	phosphomannomutase 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0011260	abnormal head mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22157680
1557829	Pmm2	phosphomannomutase 2	gene	MP:0011352	proximal convoluted tubule brush border loss		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0012325	decreased circulating antithrombin level		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557829	Pmm2	phosphomannomutase 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557829	Pmm2	phosphomannomutase 2	gene	MP:0014045	Mallory bodies		IAGP		N	RGD:5509061	20161229	MGI			PMID:27053713
1557829	Pmm2	phosphomannomutase 2	gene	MP:0030387	large posterior fontanelle		IAGP		N	RGD:5509061	20171207	MGI			PMID:27053713
1557830	Tas2r102	taste receptor, type 2, member 102	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20190502	MGI			
1557830	Tas2r102	taste receptor, type 2, member 102	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1557830	Tas2r102	taste receptor, type 2, member 102	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20250508	MGI			
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000373	belly spot		IEA		N	RGD:5509061	20111116	MGI			
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000460	mandible hypoplasia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250320
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0001304	cataract		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250320
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0001677	absent apical ectodermal ridge		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0001704	abnormal dorsal-ventral axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250320
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0003142	anotia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0003864	abnormal midbrain development		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0004474	enlarged nasal bone		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0004837	abnormal neural fold formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1731393
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0004870	small premaxilla		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0008273	abnormal intramembranous bone ossification		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0008534	enlarged fourth ventricle		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0009048	enlarged tectum		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0011697	lens vacuoles		IEA		N	RGD:5509061	20141003	MGI			
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0012091	increased midbrain size		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0012675	enlarged floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23332756
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0020393	increased neuronal precursor proliferation		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0030198	nasal septum hypoplasia		IAGP		N	RGD:5509061	20221013	MGI			PMID:34887903
1557831	Gpr161	G protein-coupled receptor 161	gene	MP:0031442	enlarged cerebral aqueduct		IAGP		N	RGD:5509061	20221103	MGI			PMID:34887903
1557832	Glod5	glyoxalase domain containing 5	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557833	Zfp467	zinc finger protein 467	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0003797	abnormal compact bone morphology		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0009269	decreased fat cell size		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0010872	increased trabecular bone mass		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0010932	increased trabecular bone connectivity density		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0010961	increased compact bone mass		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0010968	decreased compact bone area		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0013618	decreased areal bone mineral density		IAGP		N	RGD:5509061	20220922	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557833	Zfp467	zinc finger protein 467	gene	MP:0031008	decreased bone marrow adipose tissue amount		IAGP		N	RGD:5509061	20210610	MGI			PMID:33359894
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0000789	thickened cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22516202
1557834	Smarca1	SNF2 related chromatin remodeling ATPase 1	gene	MP:0014560	increased cortical ventricular zone cell density		IAGP		N	RGD:5509061	20241031	MGI			PMID:22516202
1557835	Stk26	serine/threonine kinase 26	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0000639	abnormal adrenal gland morphology		IEA		N	RGD:5509061	20200514	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0000642	enlarged adrenal glands		IEA		N	RGD:5509061	20200514	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0000681	abnormal thyroid gland morphology		IEA		N	RGD:5509061	20200514	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20200514	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1557835	Stk26	serine/threonine kinase 26	gene	MP:0003450	enlarged pancreas		IEA		N	RGD:5509061	20200514	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20210513	MGI			PMID:32271880
1557835	Stk26	serine/threonine kinase 26	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1557835	Stk26	serine/threonine kinase 26	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1557835	Stk26	serine/threonine kinase 26	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20210826	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20200514	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20220811	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0008039	increased NK T cell number		IEA		N	RGD:5509061	20210520	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1557835	Stk26	serine/threonine kinase 26	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1557835	Stk26	serine/threonine kinase 26	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1557835	Stk26	serine/threonine kinase 26	gene	MP:0013958	decreased small intestine length		IAGP		N	RGD:5509061	20230629	MGI			PMID:34240584
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230119	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230119	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001672	abnormal embryo development		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001701	incomplete embryo turning		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001712	abnormal placenta development		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001716	abnormal placenta labyrinth morphology		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001787	pericardial edema		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0005031	abnormal trophoblast layer morphology		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0005244	hemopericardium		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0006051	brainstem hemorrhage		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0010395	abnormal pharyngeal arch development		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20250206	MGI			PMID:39631040
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0012176	abnormal head development		IEA		N	RGD:5509061	20251211	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230119	MGI			
1557836	Traf7	TNF receptor-associated factor 7	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20230119	MGI			
1557837	Mxd1	MAX dimerization protein 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9451002
1557837	Mxd1	MAX dimerization protein 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9451002
1557837	Mxd1	MAX dimerization protein 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9451002
1557837	Mxd1	MAX dimerization protein 1	gene	MP:0008250	abnormal myeloid leukocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9451002
1557838	Foxp3	forkhead box P3	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000018	small ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0000019	thick ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000020	scaly ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0000020	scaly ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000414	alopecia		IEA		N	RGD:5509061	20111116	MGI			
1557838	Foxp3	forkhead box P3	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0000465	gastrointestinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780990
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1557838	Foxp3	forkhead box P3	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20200618	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20072126
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780990
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16590412
1557838	Foxp3	forkhead box P3	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16590412
1557838	Foxp3	forkhead box P3	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780990
1557838	Foxp3	forkhead box P3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1557838	Foxp3	forkhead box P3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16590412
1557838	Foxp3	forkhead box P3	gene	MP:0001198	tight skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1557838	Foxp3	forkhead box P3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780990
1557838	Foxp3	forkhead box P3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16590412
1557838	Foxp3	forkhead box P3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:16590412
1557838	Foxp3	forkhead box P3	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0001655	multifocal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661482
1557838	Foxp3	forkhead box P3	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353370
1557838	Foxp3	forkhead box P3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18209052
1557838	Foxp3	forkhead box P3	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1557838	Foxp3	forkhead box P3	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0001829	increased activated T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220874
1557838	Foxp3	forkhead box P3	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1557838	Foxp3	forkhead box P3	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1557838	Foxp3	forkhead box P3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
1557838	Foxp3	forkhead box P3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725525
1557838	Foxp3	forkhead box P3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20170427	MGI			PMID:17207605
1557838	Foxp3	forkhead box P3	gene	MP:0001863	blood vessel inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20170427	MGI			PMID:17207605
1557838	Foxp3	forkhead box P3	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1557838	Foxp3	forkhead box P3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16590412
1557838	Foxp3	forkhead box P3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16590412
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16590412
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220874
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353370
1557838	Foxp3	forkhead box P3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20072126
1557838	Foxp3	forkhead box P3	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
1557838	Foxp3	forkhead box P3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780990
1557838	Foxp3	forkhead box P3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15795373
1557838	Foxp3	forkhead box P3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220874
1557838	Foxp3	forkhead box P3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0002221	abnormal lymph organ size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0002281	abnormal respiratory mucosa goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0002344	abnormal lymph node B cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002347	abnormal lymph node T cell domain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20072126
1557838	Foxp3	forkhead box P3	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
1557838	Foxp3	forkhead box P3	gene	MP:0002413	abnormal megakaryocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661482
1557838	Foxp3	forkhead box P3	gene	MP:0002420	abnormal adaptive immunity		IAGP		N	RGD:5509061	20240613	MGI			PMID:38329807
1557838	Foxp3	forkhead box P3	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
1557838	Foxp3	forkhead box P3	gene	MP:0002435	abnormal effector T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18504307
1557838	Foxp3	forkhead box P3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20250925	MGI			PMID:36078047
1557838	Foxp3	forkhead box P3	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20240613	MGI			PMID:38329807
1557838	Foxp3	forkhead box P3	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0002496	increased IgD level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0002500	granulomatous inflammation		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0002534	abnormal type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
1557838	Foxp3	forkhead box P3	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002599	increased mean platelet volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661482
1557838	Foxp3	forkhead box P3	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002670	absent scrotum		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0002771	absent prostate gland anterior lobe		IEA		N	RGD:5509061	20111116	MGI			
1557838	Foxp3	forkhead box P3	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
1557838	Foxp3	forkhead box P3	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661482
1557838	Foxp3	forkhead box P3	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0003292	melena		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0003427	parakeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0003550	short perineum		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0003642	absent seminal vesicle		IEA		N	RGD:5509061	20111116	MGI			
1557838	Foxp3	forkhead box P3	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1557838	Foxp3	forkhead box P3	gene	MP:0003853	dry skin		IEA		N	RGD:5509061	20111116	MGI			
1557838	Foxp3	forkhead box P3	gene	MP:0003865	lymph node inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0003936	abnormal reproductive system development		IEA		N	RGD:5509061	20111116	MGI			
1557838	Foxp3	forkhead box P3	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1557838	Foxp3	forkhead box P3	gene	MP:0004392	abnormal CD8-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240620	MGI			PMID:33355624
1557838	Foxp3	forkhead box P3	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
1557838	Foxp3	forkhead box P3	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20150730	MGI			PMID:26077720
1557838	Foxp3	forkhead box P3	gene	MP:0004941	abnormal regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0004941	abnormal regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20072126
1557838	Foxp3	forkhead box P3	gene	MP:0004941	abnormal regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21468021
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18209052
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21468021
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20240620	MGI			PMID:33355624
1557838	Foxp3	forkhead box P3	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20170427	MGI			PMID:17207605
1557838	Foxp3	forkhead box P3	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0004969	pale kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0004972	abnormal regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
1557838	Foxp3	forkhead box P3	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17481928
1557838	Foxp3	forkhead box P3	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
1557838	Foxp3	forkhead box P3	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1557838	Foxp3	forkhead box P3	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21435587
1557838	Foxp3	forkhead box P3	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23805138
1557838	Foxp3	forkhead box P3	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18209052
1557838	Foxp3	forkhead box P3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20072126
1557838	Foxp3	forkhead box P3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21460251
1557838	Foxp3	forkhead box P3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20240620	MGI			PMID:33355624
1557838	Foxp3	forkhead box P3	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1557838	Foxp3	forkhead box P3	gene	MP:0004975	absent regulatory T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20072126
1557838	Foxp3	forkhead box P3	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17353370
1557838	Foxp3	forkhead box P3	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20240627	MGI			PMID:38438357
1557838	Foxp3	forkhead box P3	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0005159	azoospermia		IEA		N	RGD:5509061	20111116	MGI			
1557838	Foxp3	forkhead box P3	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20072126
1557838	Foxp3	forkhead box P3	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1557838	Foxp3	forkhead box P3	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:15780990
1557838	Foxp3	forkhead box P3	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:23281398
1557838	Foxp3	forkhead box P3	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20240620	MGI			PMID:33355624
1557838	Foxp3	forkhead box P3	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17220876
1557838	Foxp3	forkhead box P3	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21460251
1557838	Foxp3	forkhead box P3	gene	MP:0005639	hemosiderosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0006413	increased T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0008049	increased memory T cell number		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240613	MGI			PMID:38329807
1557838	Foxp3	forkhead box P3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
1557838	Foxp3	forkhead box P3	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
1557838	Foxp3	forkhead box P3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20240620	MGI			PMID:33355624
1557838	Foxp3	forkhead box P3	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24164480
1557838	Foxp3	forkhead box P3	gene	MP:0008092	abnormal T-helper 2 cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20200618	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0008141	decreased small intestinal microvillus size		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0008234	absent spleen marginal zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19661482
1557838	Foxp3	forkhead box P3	gene	MP:0008255	decreased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20240613	MGI			PMID:38329807
1557838	Foxp3	forkhead box P3	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20240620	MGI			PMID:33355624
1557838	Foxp3	forkhead box P3	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008559	abnormal interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1557838	Foxp3	forkhead box P3	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
1557838	Foxp3	forkhead box P3	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008602	increased circulating interleukin-4 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0008614	increased circulating interleukin-17 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008626	increased circulating interleukin-5 level		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18387831
1557838	Foxp3	forkhead box P3	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17581588
1557838	Foxp3	forkhead box P3	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0008698	abnormal interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18725527
1557838	Foxp3	forkhead box P3	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18845758
1557838	Foxp3	forkhead box P3	gene	MP:0008894	abnormal intraepithelial T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20072126
1557838	Foxp3	forkhead box P3	gene	MP:0009675	orthokeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17136045
1557838	Foxp3	forkhead box P3	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23135404
1557838	Foxp3	forkhead box P3	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12612578
1557838	Foxp3	forkhead box P3	gene	MP:0010183	abnormal CD4-positive helper T cell morphology		IAGP		N	RGD:5509061	20240627	MGI			PMID:34709178
1557838	Foxp3	forkhead box P3	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20201029	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20240613	MGI			PMID:38329807
1557838	Foxp3	forkhead box P3	gene	MP:0010334	pleural effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0011015	decreased body surface temperature		IAGP		N	RGD:5509061	20161124	MGI			PMID:26317471
1557838	Foxp3	forkhead box P3	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:2320565
1557838	Foxp3	forkhead box P3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16275384
1557838	Foxp3	forkhead box P3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17273171
1557838	Foxp3	forkhead box P3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7930593
1557838	Foxp3	forkhead box P3	gene	MP:0011224	abnormal lymph node medullary cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0011887	decreased circulating lipase level		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0012078	abnormal tail ring morphology		IAGP		N	RGD:5509061	20170309	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0012188	increased regulatory T cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24135136
1557838	Foxp3	forkhead box P3	gene	MP:0012188	increased regulatory T cell apoptosis		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557838	Foxp3	forkhead box P3	gene	MP:0012246	abnormal hepatic cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0012763	abnormal alpha-beta T cell number		IAGP		N	RGD:5509061	20240613	MGI			PMID:38329807
1557838	Foxp3	forkhead box P3	gene	MP:0013295	pancreas atrophy		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0013772	increased effector memory T-helper cell number		IAGP		N	RGD:5509061	20161013	MGI			PMID:27410049
1557838	Foxp3	forkhead box P3	gene	MP:0014262	increased spleen B cell follicle number		IAGP		N	RGD:5509061	20230706	MGI			PMID:31296356
1557838	Foxp3	forkhead box P3	gene	MP:0014263	decreased spleen B cell follicle number		IAGP		N	RGD:5509061	20240104	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0014678	increased erythrophagocytosis		IAGP		N	RGD:5509061	20250703	MGI			PMID:2053595
1557838	Foxp3	forkhead box P3	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:26317471
1557838	Foxp3	forkhead box P3	gene	MP:0031068	decreased blood oxygen saturation level		IAGP		N	RGD:5509061	20200618	MGI			PMID:26317471
1557838	Foxp3	forkhead box P3	gene	MP:0031269	increased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20231214	MGI			PMID:37277640
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20141003	MGI			
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18593568
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0005017	decreased B cell number		IEA		N	RGD:5509061	20141003	MGI			
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20141003	MGI			
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0008263	abnormal hippocampus CA1 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0009971	decreased hippocampus pyramidal cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0010014	hippocampus pyramidal cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:21900558
1557842	Trib2	tribbles pseudokinase 2	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0000955	abnormal spinal cord morphology		IEA		N	RGD:5509061	20210826	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210826	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210826	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20220519	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20211021	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20211021	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20240523	MGI			
1557844	Gipc3	GIPC PDZ domain containing family, member 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16426780
1557847	Klhl24	kelch-like 24	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230223	MGI			PMID:27798626
1557847	Klhl24	kelch-like 24	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20230223	MGI			PMID:27798626
1557847	Klhl24	kelch-like 24	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230223	MGI			PMID:27798626
1557847	Klhl24	kelch-like 24	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20230223	MGI			PMID:27798626
1557847	Klhl24	kelch-like 24	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20230223	MGI			PMID:27798626
1557850	Irx2	Iroquois homeobox 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14585979
1557851	Acrbp	proacrosin binding protein	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994540
1557851	Acrbp	proacrosin binding protein	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220421	MGI			PMID:30606959
1557851	Acrbp	proacrosin binding protein	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20220421	MGI			PMID:30606959
1557851	Acrbp	proacrosin binding protein	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220421	MGI			PMID:30606959
1557851	Acrbp	proacrosin binding protein	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20220421	MGI			PMID:30606959
1557851	Acrbp	proacrosin binding protein	gene	MP:0005411	delayed fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:11994540
1557851	Acrbp	proacrosin binding protein	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0009282	decreased hyperactivated sperm motility		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220421	MGI			PMID:30606959
1557851	Acrbp	proacrosin binding protein	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0030977	impaired sperm-egg recognition		IAGP		N	RGD:5509061	20220421	MGI			PMID:30606959
1557851	Acrbp	proacrosin binding protein	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0031009	abnormal sperm-egg fusion		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557851	Acrbp	proacrosin binding protein	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20220421	MGI			PMID:30606959
1557851	Acrbp	proacrosin binding protein	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220303	MGI			PMID:27303034
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339556
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339556
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15145948
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339556
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339556
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10550330
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0003329	amyloid beta deposits		IAGP		N	RGD:5509061	20141003	MGI			PMID:10550330
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9069289
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:9069289
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20180125	MGI			PMID:28970238
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11412310
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:9069289
1557852	Msr1	macrophage scavenger receptor 1	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:9069289
1557855	Tlcd4	TLC domain containing 4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260604	MGI			PMID:42087192
1557856	Usp26	ubiquitin specific peptidase 26	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20210923	MGI			PMID:30561524
1557856	Usp26	ubiquitin specific peptidase 26	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20210923	MGI			PMID:30561524
1557856	Usp26	ubiquitin specific peptidase 26	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20210923	MGI			PMID:30561524
1557856	Usp26	ubiquitin specific peptidase 26	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210923	MGI			PMID:30561524
1557856	Usp26	ubiquitin specific peptidase 26	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20210923	MGI			PMID:30561524
1557856	Usp26	ubiquitin specific peptidase 26	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210923	MGI			PMID:30561524
1557856	Usp26	ubiquitin specific peptidase 26	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20210923	MGI			PMID:30561524
1557856	Usp26	ubiquitin specific peptidase 26	gene	MP:0002790	decreased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20210923	MGI			PMID:30561524
1557856	Usp26	ubiquitin specific peptidase 26	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20210923	MGI			PMID:30561524
1557857	Klf8	Kruppel-like transcription factor 8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716600
1557857	Klf8	Kruppel-like transcription factor 8	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1557857	Klf8	Kruppel-like transcription factor 8	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716600
1557857	Klf8	Kruppel-like transcription factor 8	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716600
1557857	Klf8	Kruppel-like transcription factor 8	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23716600
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000313	abnormal cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0000828	abnormal fourth ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:23431188
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:23431188
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23431188
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20141003	MGI			PMID:23431188
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0004276	abnormal medial ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23431188
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0009703	decreased birth body size		IEA		N	RGD:5509061	20111116	MGI			
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0009820	abnormal liver vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0011087	neonatal lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23431188
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0011523	thin placenta labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23824717
1557858	Ubr4	ubiquitin protein ligase E3 component n-recognin 4	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0005670	abnormal white adipose tissue physiology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0008964	decreased carbon dioxide production		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20240215	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0031600	increased white adipose tissue apoptosis		IAGP		N	RGD:5509061	20240229	MGI			PMID:35436587
1557859	Serpina3c	serine (or cysteine) peptidase inhibitor, clade A, member 3C	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240418	MGI			PMID:35436587
1557860	Polr3b	polymerase (RNA) III (DNA directed) polypeptide B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20190502	MGI			
1557860	Polr3b	polymerase (RNA) III (DNA directed) polypeptide B	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557860	Polr3b	polymerase (RNA) III (DNA directed) polypeptide B	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008080	abnormal CD8-positive, alpha-beta T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008193	abnormal marginal zone B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557861	Sash3	SAM and SH3 domain containing 3	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16227612
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15256482
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887680
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15314648
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887680
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925582
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0000925	abnormal floor plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887680
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0000927	small floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887680
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887680
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887680
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925582
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925582
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0002958	cerebral aqueductal stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925582
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0006007	abnormal basal ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925582
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0009717	absent subcommissural organ		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925582
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887680
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0011058	abnormal spinal cord motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887680
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19887680
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12925582
1557863	Rfx4	regulatory factor X, 4 (influences HLA class II expression)	gene	MP:0014402	abnormal Reissner's fiber morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:12925582
1557864	Helq	helicase, POLQ-like	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0001132	absent mature ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210520	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20210826	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0002759	abnormal caudal vertebrae morphology		IEA		N	RGD:5509061	20220811	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210520	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0003205	testicular atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20231207	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0004833	ovary atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20231207	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20231207	MGI			
1557864	Helq	helicase, POLQ-like	gene	MP:0010288	increased gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557864	Helq	helicase, POLQ-like	gene	MP:0012437	increased Harderian gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24005329
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20180222	MGI			PMID:27892606
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20180222	MGI			PMID:27892606
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20180222	MGI			PMID:27892606
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20190404	MGI			PMID:28179432
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27892606
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20180222	MGI			PMID:27892606
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0002191	abnormal artery morphology		IAGP		N	RGD:5509061	20230824	MGI			PMID:33762433
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0003390	lymphedema		IAGP		N	RGD:5509061	20190404	MGI			PMID:28179432
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0005634	decreased circulating sodium level		IEA		N	RGD:5509061	20220519	MGI			
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20190404	MGI			PMID:28179432
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0009931	abnormal skin appearance		IEA		N	RGD:5509061	20160811	MGI			
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0010392	prolonged QRS complex duration		IEA		N	RGD:5509061	20220519	MGI			
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20180222	MGI			PMID:27892606
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0011239	abnormal skin coloration		IAGP		N	RGD:5509061	20180222	MGI			PMID:27892606
1557866	Svep1	sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1	gene	MP:0012269	nuchal edema		IAGP		N	RGD:5509061	20190404	MGI			PMID:28179432
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20210128	MGI			
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20230601	MGI			
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160317	MGI			PMID:25211221
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20241121	MGI			
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0003231	abnormal placenta vasculature		IEA		N	RGD:5509061	20210826	MGI			
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20210826	MGI			
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1557867	Arhgap28	Rho GTPase activating protein 28	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717301
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098440
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828895
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407108
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152493
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24441828
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666671
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890976
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:18419777
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:19603549
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152493
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16785989
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002036	increased rhabdomyosarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16785989
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141225	MGI			PMID:24743769
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002189	abnormal myocardial trabeculae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002190	disorganized myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002220	large lymphoid organs		IAGP		N	RGD:5509061	20160421	MGI			PMID:25087098
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002357	abnormal spleen white pulp morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:25087098
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666671
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666671
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0002972	abnormal cardiac muscle contractility		IAGP		N	RGD:5509061	20141218	MGI			PMID:24441828
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0003057	abnormal epicardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0003412	abnormal afterhyperpolarization		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666671
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098440
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666671
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004086	absent heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098440
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828895
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23363625
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004122	abnormal sinus arrhythmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873551
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18419777
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19603549
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20224043
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768539
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152493
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141218	MGI			PMID:24441828
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141225	MGI			PMID:24743769
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20180111	MGI			PMID:25775566
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20210422	MGI			PMID:33536282
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:19603549
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098440
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20210422	MGI			PMID:33536282
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16785989
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20160421	MGI			PMID:25087098
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004955	increased thymus weight		IAGP		N	RGD:5509061	20160421	MGI			PMID:25087098
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873551
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098440
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20160421	MGI			PMID:25087098
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873551
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098440
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141225	MGI			PMID:24743769
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20180111	MGI			PMID:25775566
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20210422	MGI			PMID:33536282
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20210422	MGI			PMID:33536282
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0006110	ventricular fibrillation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890976
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0006110	ventricular fibrillation		IAGP		N	RGD:5509061	20180111	MGI			PMID:25775566
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0006110	ventricular fibrillation		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20160421	MGI			PMID:25087098
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008543	atrial fibrillation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22828895
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20224043
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743453
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15890976
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873551
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18419777
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098440
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21743453
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0008950	ventricular tachycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21768539
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0009559	thymus cortex hyperplasia		IAGP		N	RGD:5509061	20160421	MGI			PMID:25087098
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873551
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098440
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152493
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0009732	ventricular premature beat		IAGP		N	RGD:5509061	20260618	MGI			PMID:20224043
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21098440
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0010505	abnormal T wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20190228	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0010637	sinus bradycardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22869620
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23666671
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180111	MGI			PMID:25775566
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210422	MGI			PMID:33536282
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23152493
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141225	MGI			PMID:24743769
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141218	MGI			PMID:24441828
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483626
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011390	abnormal fetal cardiomyocyte physiology		IAGP		N	RGD:5509061	20240404	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20210422	MGI			PMID:33536282
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0014253	decreased paired-pulse ratio		IAGP		N	RGD:5509061	20230706	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0014623	abnormal brain theta wave pattern		IAGP		N	RGD:5509061	20250306	MGI			PMID:27482086
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0020346	abnormal myocardial fiber calcium currents		IAGP		N	RGD:5509061	20210422	MGI			PMID:33536282
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0020347	abnormal myocardial fiber sodium currents		IAGP		N	RGD:5509061	20210422	MGI			PMID:33536282
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031607	abnormal fetal cardiomyocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031614	fetal cardiomyocyte vacuoles		IAGP		N	RGD:5509061	20240404	MGI			PMID:9628868
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:17431507
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031634	decreased heart right ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:16873551
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031709	ventricular arrhythmia		IAGP		N	RGD:5509061	20260514	MGI			PMID:15890976
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031709	ventricular arrhythmia		IAGP		N	RGD:5509061	20260618	MGI			PMID:33536282
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031710	polymorphic ventricular tachycardia		IAGP		N	RGD:5509061	20260514	MGI			PMID:15890976
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031710	polymorphic ventricular tachycardia		IAGP		N	RGD:5509061	20260618	MGI			PMID:20224043
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031713	bidirectional ventricular tachycardia		IAGP		N	RGD:5509061	20260514	MGI			PMID:15890976
1557868	Ryr2	ryanodine receptor 2, cardiac	gene	MP:0031713	bidirectional ventricular tachycardia		IAGP		N	RGD:5509061	20260618	MGI			PMID:20224043
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0000267	abnormal heart development		IEA		N	RGD:5509061	20111116	MGI			
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0000433	microcephaly		IEA		N	RGD:5509061	20111116	MGI			
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0001695	abnormal gastrulation		IEA		N	RGD:5509061	20111116	MGI			
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0002230	abnormal primitive streak formation		IEA		N	RGD:5509061	20111116	MGI			
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0002231	abnormal primitive streak morphology		IEA		N	RGD:5509061	20111116	MGI			
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0004073	caudal body truncation		IEA		N	RGD:5509061	20240118	MGI			
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0004180	failure of initiation of embryo turning		IEA		N	RGD:5509061	20111116	MGI			
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20111116	MGI			
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0009657	failure of chorioallantoic fusion		IEA		N	RGD:5509061	20111116	MGI			
1557870	Rps6ka6	ribosomal protein S6 kinase A6	gene	MP:0012082	delayed heart development		IEA		N	RGD:5509061	20240118	MGI			
1557871	Ly75	lymphocyte antigen 75	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10784619
1557871	Ly75	lymphocyte antigen 75	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15024047
1557871	Ly75	lymphocyte antigen 75	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22736794
1557874	Prpf38b	PRP38 pre-mRNA processing factor 38 (yeast) domain containing B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557875	Zfp398	zinc finger protein 398	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20210128	MGI			
1557875	Zfp398	zinc finger protein 398	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20241121	MGI			
1557875	Zfp398	zinc finger protein 398	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
1557875	Zfp398	zinc finger protein 398	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220811	MGI			
1557875	Zfp398	zinc finger protein 398	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210128	MGI			
1557875	Zfp398	zinc finger protein 398	gene	MP:0009477	small cecum		IEA		N	RGD:5509061	20210128	MGI			
1557876	Rad51c	RAD51 paralog C	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0001134	absent corpus luteum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0001145	abnormal male reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20471405
1557876	Rad51c	RAD51 paralog C	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20471405
1557876	Rad51c	RAD51 paralog C	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17312021
1557876	Rad51c	RAD51 paralog C	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20471405
1557878	Wdr53	WD repeat domain 53	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1557878	Wdr53	WD repeat domain 53	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1557878	Wdr53	WD repeat domain 53	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1557878	Wdr53	WD repeat domain 53	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20230601	MGI			
1557878	Wdr53	WD repeat domain 53	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1557878	Wdr53	WD repeat domain 53	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1557878	Wdr53	WD repeat domain 53	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20230601	MGI			
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0000717	abnormal lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404475
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966553
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774582
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613797
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966553
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774582
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613797
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774582
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212118
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613797
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002406	increased susceptibility to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404475
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002433	abnormal T-helper 1 cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404475
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002434	abnormal T-helper 2 cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404475
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966553
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613797
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323694
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404475
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966553
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539156
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212118
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966553
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323694
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123745
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16365433
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774582
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323694
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123745
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404475
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127454
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962259
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22683123
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22683123
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11323694
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11404475
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539156
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008036	abnormal NK T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23430111
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15749842
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212118
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613797
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008041	absent NK T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15749842
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613797
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008042	abnormal NK T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23430111
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539156
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12966553
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008176	abnormal germinal center B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613797
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212118
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613797
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15749842
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22613797
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774582
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774582
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212118
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212118
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212118
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18212118
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15774582
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22683123
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22683124
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23430111
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23430111
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0009058	decreased interleukin-21 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0010084	abnormal long lived plasma cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20153220
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22683124
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11323694
1557879	Sh2d1a	SH2 domain containing 1A	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11404475
1557880	Dmrtb1	DMRT-like family B with proline-rich C-terminal, 1	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25249458
1557880	Dmrtb1	DMRT-like family B with proline-rich C-terminal, 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20160225	MGI			PMID:25249458
1557880	Dmrtb1	DMRT-like family B with proline-rich C-terminal, 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20160225	MGI			PMID:25249458
1557880	Dmrtb1	DMRT-like family B with proline-rich C-terminal, 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25249458
1557880	Dmrtb1	DMRT-like family B with proline-rich C-terminal, 1	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:25249458
1557880	Dmrtb1	DMRT-like family B with proline-rich C-terminal, 1	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20160225	MGI			PMID:25249458
1557880	Dmrtb1	DMRT-like family B with proline-rich C-terminal, 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20160225	MGI			PMID:25249458
1557880	Dmrtb1	DMRT-like family B with proline-rich C-terminal, 1	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20160225	MGI			PMID:25249458
1557880	Dmrtb1	DMRT-like family B with proline-rich C-terminal, 1	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20160225	MGI			PMID:25249458
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20181227	MGI			
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0002942	decreased circulating alanine transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20201231	MGI			
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0020512	abnormal dendritic mushroom spine morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0020514	abnormal dendritic thin spine morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557881	Ftsj1	FtsJ RNA 2'-O-methyltransferase 1	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20221013	MGI			PMID:33771871
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690082
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15734838
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15734838
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15734838
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15734838
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690082
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690082
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15734838
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690082
1557883	Stxbp3	syntaxin binding protein 3	gene	MP:0015003	decreased embryo length		IAGP		N	RGD:5509061	20260611	MGI			PMID:15690082
1557886	Nup62	nucleoporin 62	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210128	MGI			
1557886	Nup62	nucleoporin 62	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1557886	Nup62	nucleoporin 62	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1557886	Nup62	nucleoporin 62	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20190502	MGI			
1557886	Nup62	nucleoporin 62	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1557886	Nup62	nucleoporin 62	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557886	Nup62	nucleoporin 62	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20210128	MGI			
1557887	Zfp512	zinc finger protein 512	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1557887	Zfp512	zinc finger protein 512	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1557887	Zfp512	zinc finger protein 512	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1557887	Zfp512	zinc finger protein 512	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20201022	MGI			
1557887	Zfp512	zinc finger protein 512	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20210826	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210826	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0004958	enlarged prostate gland		IEA		N	RGD:5509061	20210826	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20250508	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20181227	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220519	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210826	MGI			
1557888	Ulk3	unc-51-like kinase 3	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20210826	MGI			
1557889	Gspt2	G1 to S phase transition 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1557889	Gspt2	G1 to S phase transition 2	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20201022	MGI			
1557889	Gspt2	G1 to S phase transition 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20260402	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20111116	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20111116	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20111116	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748463
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748464
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10748465
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0003036	vertebral transformation		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0003063	increased coping response		IEA		N	RGD:5509061	20111116	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0003456	absent tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20230601	MGI			
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18241853
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11330864
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557890	Cer1	cerberus 1, DAN family BMP antagonist	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1557892	Hoxa13	homeobox A13	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483557
1557892	Hoxa13	homeobox A13	gene	MP:0000492	abnormal rectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783783
1557892	Hoxa13	homeobox A13	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17222543
1557892	Hoxa13	homeobox A13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22465667
1557892	Hoxa13	homeobox A13	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1557892	Hoxa13	homeobox A13	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684655
1557892	Hoxa13	homeobox A13	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385446
1557892	Hoxa13	homeobox A13	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385446
1557892	Hoxa13	homeobox A13	gene	MP:0000565	oligodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1557892	Hoxa13	homeobox A13	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684655
1557892	Hoxa13	homeobox A13	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0000661	small prostate gland ventral lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:10210434
1557892	Hoxa13	homeobox A13	gene	MP:0000666	decreased prostate gland duct number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10210434
1557892	Hoxa13	homeobox A13	gene	MP:0001135	abnormal uterine cervix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0001157	small seminal vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10210434
1557892	Hoxa13	homeobox A13	gene	MP:0001163	abnormal prostate gland anterior lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10210434
1557892	Hoxa13	homeobox A13	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684655
1557892	Hoxa13	homeobox A13	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1557892	Hoxa13	homeobox A13	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0001715	placental labyrinth hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483557
1557892	Hoxa13	homeobox A13	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1557892	Hoxa13	homeobox A13	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483557
1557892	Hoxa13	homeobox A13	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0002059	abnormal seminal vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10210434
1557892	Hoxa13	homeobox A13	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684655
1557892	Hoxa13	homeobox A13	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1557892	Hoxa13	homeobox A13	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385446
1557892	Hoxa13	homeobox A13	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0002772	brachypodia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1557892	Hoxa13	homeobox A13	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0003124	hypospadia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783783
1557892	Hoxa13	homeobox A13	gene	MP:0003230	abnormal umbilical artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684655
1557892	Hoxa13	homeobox A13	gene	MP:0003270	intestinal obstruction		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0003550	short perineum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0003617	urinary bladder hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0003800	monodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0003800	monodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0003942	abnormal urinary system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12783783
1557892	Hoxa13	homeobox A13	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0004576	abnormal embryonic autopod plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0004641	elongated metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1557892	Hoxa13	homeobox A13	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17222543
1557892	Hoxa13	homeobox A13	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0006230	iris stroma hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1557892	Hoxa13	homeobox A13	gene	MP:0006253	clinodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20141003	MGI			PMID:11543619
1557892	Hoxa13	homeobox A13	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483557
1557892	Hoxa13	homeobox A13	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0008919	fused tarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0008983	small vagina		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0009001	absent hallux		IAGP		N	RGD:5509061	20141003	MGI			PMID:17222543
1557892	Hoxa13	homeobox A13	gene	MP:0009049	abnormal hallux morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17222543
1557892	Hoxa13	homeobox A13	gene	MP:0009087	dilated uterine horn		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0009103	abnormal penile bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0009104	small penile bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0009227	uterine cervix hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0009252	absent urinary bladder		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0009740	small prostate gland dorsolateral lobe		IAGP		N	RGD:5509061	20220303	MGI			PMID:10210434
1557892	Hoxa13	homeobox A13	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684655
1557892	Hoxa13	homeobox A13	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15385446
1557892	Hoxa13	homeobox A13	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684655
1557892	Hoxa13	homeobox A13	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8898214
1557892	Hoxa13	homeobox A13	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684655
1557892	Hoxa13	homeobox A13	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0011780	abnormal female urethra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0011828	urinary bladder cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0011829	vesicovaginal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:10569982
1557892	Hoxa13	homeobox A13	gene	MP:0012302	umbilical artery stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11684655
1557892	Hoxa13	homeobox A13	gene	MP:0012302	umbilical artery stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18483557
1557892	Hoxa13	homeobox A13	gene	MP:0013318	abnormal branching involved in seminal vesicle morphogenesis		IAGP		N	RGD:5509061	20141204	MGI			PMID:10210434
1557892	Hoxa13	homeobox A13	gene	MP:0013323	abnormal ampullary gland morphology		IAGP		N	RGD:5509061	20141204	MGI			PMID:10210434
1557892	Hoxa13	homeobox A13	gene	MP:0014281	hindlimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:5519671
1557892	Hoxa13	homeobox A13	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:8898214
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20241121	MGI			
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20260402	MGI			
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:29213114
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1557893	Bcl7b	B cell CLL/lymphoma 7B	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1557894	Idnk	idnK gluconokinase homolog (E. coli)	gene	MP:0009456	impaired cued conditioning behavior		IEA		N	RGD:5509061	20141003	MGI			
1557894	Idnk	idnK gluconokinase homolog (E. coli)	gene	MP:0020220	decreased tear production		IEA		N	RGD:5509061	20141211	MGI			
1557895	Zfp202	zinc finger protein 202	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20160804	MGI			
1557895	Zfp202	zinc finger protein 202	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1557895	Zfp202	zinc finger protein 202	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160804	MGI			
1557895	Zfp202	zinc finger protein 202	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1557895	Zfp202	zinc finger protein 202	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1557895	Zfp202	zinc finger protein 202	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1557895	Zfp202	zinc finger protein 202	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1557895	Zfp202	zinc finger protein 202	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1557895	Zfp202	zinc finger protein 202	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1557897	Ntm	neurotrimin	gene	MP:0005385	cardiovascular system phenotype		IAGP		N	RGD:5509061	20201112	MGI			PMID:24616287
1557897	Ntm	neurotrimin	gene	MP:0012293	impaired active avoidance behavior		IAGP		N	RGD:5509061	20190228	MGI			PMID:27693610
1557897	Ntm	neurotrimin	gene	MP:0030586	impaired behavioral response to amphetamine		IAGP		N	RGD:5509061	20190228	MGI			PMID:27693610
1557898	Peli2	pellino 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20200409	MGI			PMID:29674674
1557898	Peli2	pellino 2	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29674674
1557898	Peli2	pellino 2	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200409	MGI			PMID:29674674
1557898	Peli2	pellino 2	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20200409	MGI			PMID:29674674
1557898	Peli2	pellino 2	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200409	MGI			PMID:29674674
1557898	Peli2	pellino 2	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20200409	MGI			PMID:29674674
1557898	Peli2	pellino 2	gene	MP:0011080	increased macrophage apoptosis		IAGP		N	RGD:5509061	20200409	MGI			PMID:29674674
1557900	Cd209b	CD209b antigen	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15583012
1557900	Cd209b	CD209b antigen	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20200618	MGI			PMID:31998663
1557900	Cd209b	CD209b antigen	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15583012
1557900	Cd209b	CD209b antigen	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200618	MGI			PMID:31998663
1557900	Cd209b	CD209b antigen	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15583012
1557900	Cd209b	CD209b antigen	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557900	Cd209b	CD209b antigen	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20200618	MGI			PMID:31998663
1557900	Cd209b	CD209b antigen	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557900	Cd209b	CD209b antigen	gene	MP:0005635	decreased circulating bilirubin level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557900	Cd209b	CD209b antigen	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557900	Cd209b	CD209b antigen	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557900	Cd209b	CD209b antigen	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557900	Cd209b	CD209b antigen	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200618	MGI			PMID:20130211
1557900	Cd209b	CD209b antigen	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200618	MGI			PMID:20130211
1557900	Cd209b	CD209b antigen	gene	MP:0008685	decreased interleukin-18 secretion		IAGP		N	RGD:5509061	20200618	MGI			PMID:20130211
1557900	Cd209b	CD209b antigen	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20200618	MGI			PMID:20130211
1557900	Cd209b	CD209b antigen	gene	MP:0009646	urinary bladder inflammation		IAGP		N	RGD:5509061	20200618	MGI			PMID:31998663
1557900	Cd209b	CD209b antigen	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200618	MGI			PMID:15583012
1557900	Cd209b	CD209b antigen	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1557901	Pdp2	pyruvate dehydrogenase phosphatase catalytic subunit 2	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1557902	Cul4b	cullin 4B	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763239
1557902	Cul4b	cullin 4B	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0001693	failure of primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0001717	absent ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0002084	abnormal developmental patterning		IEA		N	RGD:5509061	20111116	MGI			
1557902	Cul4b	cullin 4B	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763239
1557902	Cul4b	cullin 4B	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0004266	pale placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763239
1557902	Cul4b	cullin 4B	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763239
1557902	Cul4b	cullin 4B	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763239
1557902	Cul4b	cullin 4B	gene	MP:0010382	abnormal dosage compensation, by inactivation of X chromosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0011527	disorganized placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:22453236
1557902	Cul4b	cullin 4B	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:22606329
1557902	Cul4b	cullin 4B	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:22763239
1557904	Hook2	hook microtubule tethering protein 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1557904	Hook2	hook microtubule tethering protein 2	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20210520	MGI			
1557904	Hook2	hook microtubule tethering protein 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1557904	Hook2	hook microtubule tethering protein 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1557904	Hook2	hook microtubule tethering protein 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1557904	Hook2	hook microtubule tethering protein 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20220519	MGI			
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20250508	MGI			
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0001410	head bobbing		IEA		N	RGD:5509061	20250508	MGI			
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0005400	abnormal vitamin level		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0012604	decreased glutathione level		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0030692	decreased serine level		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557905	Naxd	NAD(P)HX dehydratase	gene	MP:0030695	decreased circulating serine level		IAGP		N	RGD:5509061	20260806	MGI			PMID:41747729
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001152	increased Leydig cell number		IAGP		N	RGD:5509061	20160204	MGI			PMID:26248850
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20160204	MGI			PMID:26248850
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20160204	MGI			PMID:26248850
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20160204	MGI			PMID:26248850
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20160204	MGI			PMID:26248850
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0009377	ectopic manchette		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0013598	Leydig cell hypertrophy		IAGP		N	RGD:5509061	20160204	MGI			PMID:26248850
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220623	MGI			PMID:26248850
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20220721	MGI			PMID:26853561
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557906	Rfx2	regulatory factor X, 2 (influences HLA class II expression)	gene	MP:0031389	abnormal ectoplasmic specialization morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:26162102
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0006038	increased mitochondrial fission		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0020337	abnormal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557907	Dnajc30	DnaJ heat shock protein family (Hsp40) member C30	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20190321	MGI			PMID:30318146
1557910	Slc6a11	solute carrier family 6 (neurotransmitter transporter, GABA), member 11	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IEA		N	RGD:5509061	20111116	MGI			
1557910	Slc6a11	solute carrier family 6 (neurotransmitter transporter, GABA), member 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1557912	Ifitm3	interferon induced transmembrane protein 3	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:24278312
1557912	Ifitm3	interferon induced transmembrane protein 3	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:22446628
1557912	Ifitm3	interferon induced transmembrane protein 3	gene	MP:0031046	increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:22446628
1557915	Acer1	alkaline ceramidase 1	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0000652	enlarged sebaceous gland		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001239	abnormal epidermis stratum granulosum morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0002992	abnormal sebaceous lipid secretion		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0003810	abnormal hair cuticle		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0008858	abnormal hair cycle anagen phase		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0008860	abnormal hair cycle telogen phase		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009288	increased epididymal fat pad weight		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009441	delayed skin barrier formation		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009535	abnormal skin sebaceous gland morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009602	abnormal keratohyalin granule morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009793	sebaceous gland hypertrophy		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0010682	abnormal hair follicle infundibulum morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0010683	dilated hair follicle infundibulum		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0010683	dilated hair follicle infundibulum		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0011194	abnormal hair follicle physiology		IAGP		N	RGD:5509061	20180301	MGI			PMID:29056331
1557915	Acer1	alkaline ceramidase 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0013375	abnormal sebocyte morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0014169	decreased brown adipose tissue mass		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0020117	decreased sphingosine level		IAGP		N	RGD:5509061	20161117	MGI			PMID:27126290
1557915	Acer1	alkaline ceramidase 1	gene	MP:0030570	abnormal piliary canal morphology		IAGP		N	RGD:5509061	20180524	MGI			PMID:29056331
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875044
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001106	abnormal Schwann cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875044
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20141003	MGI			
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20141003	MGI			
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875044
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001504	abnormal posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875044
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9418970
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9126326
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256488
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9418970
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12719378
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875044
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16223892
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20180830	MGI			PMID:27124591
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0005284	increased saturated fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9256488
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875044
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11875044
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0008288	abnormal adrenal cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0008294	abnormal adrenal gland zona fasciculata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0008295	abnormal adrenal gland zona reticularis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15489218
1557916	Abcd1	ATP-binding cassette, sub-family D member 1	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180920	MGI			PMID:27124591
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0009848	increased horizontal stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0009849	increased vertical stereotypic behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:21775500
1557918	Zdhhc17	zinc finger, DHHC domain containing 17	gene	MP:0020083	decreased hippocampus volume		IAGP		N	RGD:5509061	20170706	MGI			PMID:21775500
1557919	Dnm3	dynamin 3	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557919	Dnm3	dynamin 3	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:21689597
1557920	Ankrd48	ankyrin repeat domain 48	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20241121	MGI			
1557920	Ankrd48	ankyrin repeat domain 48	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1557920	Ankrd48	ankyrin repeat domain 48	gene	MP:0003883	enlarged stomach		IEA		N	RGD:5509061	20241121	MGI			
1557920	Ankrd48	ankyrin repeat domain 48	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1557922	Magee2	MAGE family member E2	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20221222	MGI			PMID:34464968
1557922	Magee2	MAGE family member E2	gene	MP:0000905	increased superior colliculus size		IAGP		N	RGD:5509061	20221222	MGI			PMID:34464968
1557922	Magee2	MAGE family member E2	gene	MP:0005238	increased brain size		IAGP		N	RGD:5509061	20221222	MGI			PMID:34464968
1557922	Magee2	MAGE family member E2	gene	MP:0008228	increased anterior commissure size		IAGP		N	RGD:5509061	20221222	MGI			PMID:34464968
1557922	Magee2	MAGE family member E2	gene	MP:0012449	increased primary motor cortex size		IAGP		N	RGD:5509061	20221222	MGI			PMID:34464968
1557922	Magee2	MAGE family member E2	gene	MP:0012451	abnormal retrosplenial granular cortex morphology		IAGP		N	RGD:5509061	20221222	MGI			PMID:34464968
1557922	Magee2	MAGE family member E2	gene	MP:0012452	increased retrosplenial granular cortex size		IAGP		N	RGD:5509061	20221222	MGI			PMID:34464968
1557922	Magee2	MAGE family member E2	gene	MP:0012465	increased hippocampal fimbria size		IAGP		N	RGD:5509061	20221222	MGI			PMID:34464968
1557922	Magee2	MAGE family member E2	gene	MP:0020534	increased pons size		IAGP		N	RGD:5509061	20221222	MGI			PMID:34464968
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000066	osteoporosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000084	abnormal fontanelle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000423	delayed hair regrowth		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000427	abnormal hair cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20260716	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0000955	abnormal spinal cord morphology		IEA		N	RGD:5509061	20210826	MGI			
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001129	impaired ovarian folliculogenesis		IAGP		N	RGD:5509061	20220519	MGI			PMID:31489491
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:31489491
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001824	abnormal thymus involution		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:10691732
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10691732
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19504344
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0002835	abnormal cranial suture morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003809	abnormal hair shaft morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004030	induced chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19504344
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004228	decreased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004759	decreased mitotic index		IAGP		N	RGD:5509061	20141003	MGI			PMID:19504344
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004856	decreased ovary weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0004970	kidney atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:31489491
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160421	MGI			
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0005631	decreased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0008404	increased cellular sensitivity to methylmethanesulfonate induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0008974	proportional dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0009362	abnormal primary ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0009794	sebaceous gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0009949	abnormal olfactory bulb granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10691732
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10801416
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011120	increased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:31489491
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:31489491
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011346	renal tubule atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011363	renal glomerulus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18371340
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011495	abnormal head shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0011496	abnormal head size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0012525	abnormal rhombic lip morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20240523	MGI			
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0013501	increased fibroblast apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0013508	increased granulosa cell apoptosis		IAGP		N	RGD:5509061	20220519	MGI			PMID:31489491
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0013551	decreased cerebellar granule cell precursor proliferation		IAGP		N	RGD:5509061	20161201	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0020576	decreased corpus callosum cell number		IAGP		N	RGD:5509061	20260716	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0020594	decreased cerebral cortex cell number		IAGP		N	RGD:5509061	20260716	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0030004	hippocampus hypoplasia		IAGP		N	RGD:5509061	20170706	MGI			PMID:22266795
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0030048	sloping forehead		IAGP		N	RGD:5509061	20170921	MGI			PMID:19620979
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0031018	decreased granulosa cell proliferation		IAGP		N	RGD:5509061	20220519	MGI			PMID:31489491
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0031019	increased granulosa cell proliferation		IAGP		N	RGD:5509061	20220519	MGI			PMID:31489491
1557923	Atr	ataxia telangiectasia and Rad3 related	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220519	MGI			PMID:31489491
1557925	Rspo4	R-spondin 4	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20221110	MGI			
1557926	Krt16	keratin 16	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0000763	abnormal filiform papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557926	Krt16	keratin 16	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22336941
1557927	Eif3c	eukaryotic translation initiation factor 3, subunit C	gene	MP:0000373	belly spot		IEA		N	RGD:5509061	20111116	MGI			
1557927	Eif3c	eukaryotic translation initiation factor 3, subunit C	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20111116	MGI			
1557927	Eif3c	eukaryotic translation initiation factor 3, subunit C	gene	MP:0001732	postnatal growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1557927	Eif3c	eukaryotic translation initiation factor 3, subunit C	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20111116	MGI			
1557927	Eif3c	eukaryotic translation initiation factor 3, subunit C	gene	MP:0002177	abnormal outer ear morphology		IEA		N	RGD:5509061	20111116	MGI			
1557927	Eif3c	eukaryotic translation initiation factor 3, subunit C	gene	MP:0002938	white spotting		IEA		N	RGD:5509061	20111116	MGI			
1557927	Eif3c	eukaryotic translation initiation factor 3, subunit C	gene	MP:0002939	head spot		IEA		N	RGD:5509061	20111116	MGI			
1557927	Eif3c	eukaryotic translation initiation factor 3, subunit C	gene	MP:0008770	decreased survivor rate		IEA		N	RGD:5509061	20111116	MGI			
1557927	Eif3c	eukaryotic translation initiation factor 3, subunit C	gene	MP:0009049	abnormal hallux morphology		IEA		N	RGD:5509061	20111116	MGI			
1557928	Zdhhc8	zinc finger, DHHC domain containing 8	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:15184899
1557928	Zdhhc8	zinc finger, DHHC domain containing 8	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:18836441
1557928	Zdhhc8	zinc finger, DHHC domain containing 8	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:15184899
1557928	Zdhhc8	zinc finger, DHHC domain containing 8	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:18836441
1557928	Zdhhc8	zinc finger, DHHC domain containing 8	gene	MP:0015055	decreased synapse density		IAGP		N	RGD:5509061	20260813	MGI			PMID:18836441
1557929	Rnf208	ring finger protein 208	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210826	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210826	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210826	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20210826	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20210826	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20220519	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210826	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20220811	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20210826	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20210826	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20240627	MGI			
1557929	Rnf208	ring finger protein 208	gene	MP:0011047	increased lung tissue damping		IEA		N	RGD:5509061	20220519	MGI			
1557931	Fbxo41	F-box protein 41	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20181227	MGI			
1557931	Fbxo41	F-box protein 41	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1557931	Fbxo41	F-box protein 41	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20210128	MGI			
1557931	Fbxo41	F-box protein 41	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1557931	Fbxo41	F-box protein 41	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1557931	Fbxo41	F-box protein 41	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557931	Fbxo41	F-box protein 41	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20231207	MGI			
1557931	Fbxo41	F-box protein 41	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557931	Fbxo41	F-box protein 41	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160630	MGI			PMID:26063905
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20201231	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20190502	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20230601	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IEA		N	RGD:5509061	20210520	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20201022	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20190502	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1557932	Slc44a1	solute carrier family 44, member 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20211021	MGI			
1557934	Epgn	epithelial mitogen	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20170105	MGI			
1557934	Epgn	epithelial mitogen	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23142483
1557934	Epgn	epithelial mitogen	gene	MP:0009108	increased pancreas weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23142483
1557935	Zranb3	zinc finger, RAN-binding domain containing 3	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20231207	MGI			
1557936	Tmprss11f	transmembrane protease, serine 11f	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20191003	MGI			PMID:28338078
1557936	Tmprss11f	transmembrane protease, serine 11f	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20191031	MGI			PMID:31501243
1557936	Tmprss11f	transmembrane protease, serine 11f	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20191003	MGI			PMID:28338078
1557937	Fcho2	FCH domain only 2	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1557937	Fcho2	FCH domain only 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1557937	Fcho2	FCH domain only 2	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1557937	Fcho2	FCH domain only 2	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20211021	MGI			
1557937	Fcho2	FCH domain only 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557939	Pdzd4	PDZ domain containing 4	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1557941	Kbtbd12	kelch repeat and BTB (POZ) domain containing 12	gene	MP:0000494	abnormal cecum morphology		IEA		N	RGD:5509061	20230601	MGI			
1557941	Kbtbd12	kelch repeat and BTB (POZ) domain containing 12	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20230601	MGI			
1557941	Kbtbd12	kelch repeat and BTB (POZ) domain containing 12	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1557941	Kbtbd12	kelch repeat and BTB (POZ) domain containing 12	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20230601	MGI			
1557943	Pld4	phospholipase D family member 4	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1557943	Pld4	phospholipase D family member 4	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1557943	Pld4	phospholipase D family member 4	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0000416	sparse hair		IEA		N	RGD:5509061	20120126	MGI			
1557943	Pld4	phospholipase D family member 4	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1557943	Pld4	phospholipase D family member 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20190905	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20190905	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20190905	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190905	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1557943	Pld4	phospholipase D family member 4	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20210520	MGI			
1557943	Pld4	phospholipase D family member 4	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20190905	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20210520	MGI			
1557943	Pld4	phospholipase D family member 4	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20240523	MGI			
1557943	Pld4	phospholipase D family member 4	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210520	MGI			
1557943	Pld4	phospholipase D family member 4	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20190905	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20190905	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0008244	abnormal peritoneal macrophage morphology		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20190905	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0011890	increased circulating ferritin level		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0012762	abnormal alpha-beta T cell morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0014495	increased circulating chemokine level		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0014682	increased polyploid hepatocyte number		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0014902	increased circulating CCL2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20190926	MGI			PMID:30679154
1557943	Pld4	phospholipase D family member 4	gene	MP:0031070	hemophagocytosis		IAGP		N	RGD:5509061	20200910	MGI			PMID:30111894
1557943	Pld4	phospholipase D family member 4	gene	MP:0031220	increased circulating CXCL10 level		IAGP		N	RGD:5509061	20210204	MGI			PMID:30111894
1557944	Tnrc6a	trinucleotide repeat containing 6a	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20160304	MGI			PMID:22187428
1557944	Tnrc6a	trinucleotide repeat containing 6a	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20160304	MGI			PMID:22187428
1557944	Tnrc6a	trinucleotide repeat containing 6a	gene	MP:0001724	abnormal extraembryonic endoderm formation		IAGP		N	RGD:5509061	20160304	MGI			PMID:22187428
1557944	Tnrc6a	trinucleotide repeat containing 6a	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20160304	MGI			PMID:22187428
1557944	Tnrc6a	trinucleotide repeat containing 6a	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20160304	MGI			PMID:22187428
1557944	Tnrc6a	trinucleotide repeat containing 6a	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180315	MGI			PMID:28811219
1557944	Tnrc6a	trinucleotide repeat containing 6a	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20160304	MGI			PMID:22187428
1557944	Tnrc6a	trinucleotide repeat containing 6a	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20160304	MGI			PMID:22187428
1557944	Tnrc6a	trinucleotide repeat containing 6a	gene	MP:0011204	abnormal visceral yolk sac blood island morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:22187428
1557946	Myg1	melanocyte proliferating gene 1	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19818808
1557946	Myg1	melanocyte proliferating gene 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:19818808
1557946	Myg1	melanocyte proliferating gene 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:19818808
1557946	Myg1	melanocyte proliferating gene 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19818808
1557946	Myg1	melanocyte proliferating gene 1	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:19818808
1557946	Myg1	melanocyte proliferating gene 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19818808
1557946	Myg1	melanocyte proliferating gene 1	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19818808
1557946	Myg1	melanocyte proliferating gene 1	gene	MP:0003963	abnormal corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19818808
1557947	Abca16	ATP-binding cassette, sub-family A member 16	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201022	MGI			
1557947	Abca16	ATP-binding cassette, sub-family A member 16	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20210826	MGI			
1557947	Abca16	ATP-binding cassette, sub-family A member 16	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201231	MGI			
1557947	Abca16	ATP-binding cassette, sub-family A member 16	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1557948	Phf6	PHD finger protein 6	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0003466	decreased single cell response threshold		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0003468	increased single cell response intensity		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0005120	decreased circulating growth hormone level		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0005128	decreased adrenocorticotropin level		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0005361	small pituitary gland		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0008524	increased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0008573	increased circulating interferon-alpha level		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0010168	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557948	Phf6	PHD finger protein 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20210304	MGI			PMID:32994169
1557948	Phf6	PHD finger protein 6	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0013697	decreased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0013707	abnormal hematopoietic precursor cell morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0013762	abnormal effector T cell number		IAGP		N	RGD:5509061	20220609	MGI			PMID:31395598
1557948	Phf6	PHD finger protein 6	gene	MP:0013892	increased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20210304	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0014400	increased hematopoietic precursor cell number		IAGP		N	RGD:5509061	20240321	MGI			PMID:30755422
1557948	Phf6	PHD finger protein 6	gene	MP:0020396	abnormal social recognition		IAGP		N	RGD:5509061	20190516	MGI			PMID:30403997
1557949	Shroom3	shroom family member 3	gene	MP:0000075	absent neurocranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589677
1557949	Shroom3	shroom family member 3	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589677
1557949	Shroom3	shroom family member 3	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589677
1557949	Shroom3	shroom family member 3	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589677
1557949	Shroom3	shroom family member 3	gene	MP:0000930	wavy neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589677
1557949	Shroom3	shroom family member 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20221215	MGI			
1557949	Shroom3	shroom family member 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589677
1557949	Shroom3	shroom family member 3	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20221215	MGI			
1557949	Shroom3	shroom family member 3	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20221215	MGI			
1557949	Shroom3	shroom family member 3	gene	MP:0003385	abnormal body wall morphology		IEA		N	RGD:5509061	20111116	MGI			
1557949	Shroom3	shroom family member 3	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20221215	MGI			
1557949	Shroom3	shroom family member 3	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0005155	herniated intestine		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589677
1557949	Shroom3	shroom family member 3	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20111116	MGI			
1557949	Shroom3	shroom family member 3	gene	MP:0009908	protruding tongue		IEA		N	RGD:5509061	20221215	MGI			
1557949	Shroom3	shroom family member 3	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0010433	double inlet heart left ventricle		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0010585	abnormal conotruncal ridge morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0010912	herniated liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589677
1557949	Shroom3	shroom family member 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10589677
1557949	Shroom3	shroom family member 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1557949	Shroom3	shroom family member 3	gene	MP:0011394	increased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0020414	abnormal fibroblast physiology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0021158	decreased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231207	MGI			PMID:32511952
1557949	Shroom3	shroom family member 3	gene	MP:0031525	thin left ventricle myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:32511952
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210520	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210520	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210826	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210826	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210826	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20241121	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210520	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20210520	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210520	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20210128	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1557951	Rpe	ribulose-5-phosphate-3-epimerase	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0005666	abnormal adipose tissue physiology		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0009117	abnormal white fat cell morphology		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0009118	increased white fat cell size		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0009121	increased white fat cell lipid droplet size		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0009124	increased brown fat cell lipid droplet size		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0009285	increased gonadal fat pad weight		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0009292	increased inguinal fat pad weight		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0020325	abnormal beige fat cell morphology		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0020414	abnormal fibroblast physiology		IEA		N	RGD:5509061	20200402	MGI			
1557952	Ehd2	EH-domain containing 2	gene	MP:0030016	increased adipocyte glucose uptake		IEA		N	RGD:5509061	20200402	MGI			
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20191003	MGI			PMID:28290521
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20210826	MGI			
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20191003	MGI			PMID:28290521
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20191003	MGI			PMID:28290521
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:28290521
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20191003	MGI			PMID:28290521
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20191003	MGI			PMID:28290521
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1557954	Ndrg3	N-myc downstream regulated gene 3	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20220519	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20260402	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20260402	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20260402	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20250508	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230720	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230720	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230720	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20230720	MGI			
1557957	Atp5f1b	ATP synthase F1 subunit beta	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20241121	MGI			
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20241121	MGI			
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20241121	MGI			
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611300
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611300
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0002694	abnormal pancreas secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966573
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10611300
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966573
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966573
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14966573
1557958	Gipr	gastric inhibitory polypeptide receptor	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20241121	MGI			
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0000087	absent mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0000230	abnormal systemic arterial blood pressure		IAGP		N	RGD:5509061	20250227	MGI			PMID:30804442
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0001784	abnormal fluid regulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0003719	abnormal pericyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0003814	vascular smooth muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0004038	lymphangiectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20250313	MGI			PMID:26714589
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20250227	MGI			PMID:30804442
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250227	MGI			PMID:30804442
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20713964
1557960	Lpar4	lysophosphatidic acid receptor 4	gene	MP:0014273	abnormal skin vasculature morphology		IAGP		N	RGD:5509061	20230810	MGI			PMID:20713964
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0008431	abnormal short-term spatial reference memory		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20190221	MGI			PMID:26246171
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20190221	MGI			PMID:26246171
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20190221	MGI			PMID:26246171
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0020448	increased microglial cell activation		IAGP		N	RGD:5509061	20200514	MGI			PMID:31416892
1557961	Marchf5	membrane associated ring-CH-type finger 5	gene	MP:0031023	decreased susceptibility to Riboviria infection induced morbidity/mortality		IAGP		N	RGD:5509061	20200514	MGI			PMID:26246171
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20231207	MGI			
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0009431	decreased fetal weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0011521	decreased placental labyrinth size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0011522	abnormal placental labyrinth villi morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0011525	abnormal placenta intervillous maternal lacunae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0011526	abnormal placenta fetal blood space morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0011528	abnormal placental labyrinth villi branching morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557962	Llgl2	LLGL2 scribble cell polarity complex component	gene	MP:0011529	increased placenta intervillous maternal lacunae size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21606200
1557963	Hoxb4	homeobox B4	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1557963	Hoxb4	homeobox B4	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14962901
1557963	Hoxb4	homeobox B4	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14962901
1557963	Hoxb4	homeobox B4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557963	Hoxb4	homeobox B4	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1557963	Hoxb4	homeobox B4	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14962901
1557963	Hoxb4	homeobox B4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12748289
1557963	Hoxb4	homeobox B4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14962901
1557963	Hoxb4	homeobox B4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21278354
1557963	Hoxb4	homeobox B4	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:14962901
1557963	Hoxb4	homeobox B4	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14962901
1557963	Hoxb4	homeobox B4	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0003048	abnormal cervical vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628700
1557963	Hoxb4	homeobox B4	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1557963	Hoxb4	homeobox B4	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0003388	absent pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0003924	diaphragmatic hernia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557963	Hoxb4	homeobox B4	gene	MP:0004134	abnormal chest morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557963	Hoxb4	homeobox B4	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557963	Hoxb4	homeobox B4	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557963	Hoxb4	homeobox B4	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1557963	Hoxb4	homeobox B4	gene	MP:0004608	abnormal cervical axis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557963	Hoxb4	homeobox B4	gene	MP:0004613	fusion of vertebral arches		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628700
1557963	Hoxb4	homeobox B4	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628700
1557963	Hoxb4	homeobox B4	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557963	Hoxb4	homeobox B4	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1557963	Hoxb4	homeobox B4	gene	MP:0004620	cervical vertebral fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628700
1557963	Hoxb4	homeobox B4	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0008022	dilated heart ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557963	Hoxb4	homeobox B4	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628700
1557963	Hoxb4	homeobox B4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7628700
1557963	Hoxb4	homeobox B4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557963	Hoxb4	homeobox B4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11518511
1557963	Hoxb4	homeobox B4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9012503
1557963	Hoxb4	homeobox B4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8097432
1557964	Il16	interleukin 16	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15728482
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0000217	abnormal leukocyte cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260604	MGI			PMID:41704749
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0001847	brain inflammation		IAGP		N	RGD:5509061	20260604	MGI			PMID:41704749
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16714379
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16714379
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:28031478
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16714379
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008721	abnormal chemokine level		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16625202
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16714379
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0010092	increased circulating magnesium level		IEA		N	RGD:5509061	20210128	MGI			
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0011075	abnormal macrophage activation involved in immune response		IAGP		N	RGD:5509061	20150312	MGI			PMID:24530055
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260604	MGI			PMID:41704749
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16625202
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:16714379
1557966	Ifih1	interferon induced with helicase C domain 1	gene	MP:0031301	chronic liver inflammation		IAGP		N	RGD:5509061	20211028	MGI			PMID:24530055
1557967	Vps37a	vacuolar protein sorting 37A	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20230119	MGI			
1557967	Vps37a	vacuolar protein sorting 37A	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20230119	MGI			
1557967	Vps37a	vacuolar protein sorting 37A	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20230119	MGI			
1557967	Vps37a	vacuolar protein sorting 37A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1557967	Vps37a	vacuolar protein sorting 37A	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20230119	MGI			
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18026105
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18026105
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557969	Rgs13	regulator of G-protein signaling 13	gene	MP:0008896	increased IgG2c level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23533672
1557971	Nkx1-1	NK1 homeobox 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645517
1557971	Nkx1-1	NK1 homeobox 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645517
1557971	Nkx1-1	NK1 homeobox 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645517
1557971	Nkx1-1	NK1 homeobox 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645517
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20160616	MGI			PMID:24876128
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20160616	MGI			PMID:24876128
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0001929	abnormal gametogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24876128
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24876128
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20160616	MGI			PMID:24876128
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0009137	decreased brown fat lipid droplet number		IAGP		N	RGD:5509061	20160616	MGI			PMID:24876128
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0009243	hairpin sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17242199
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0009295	decreased interscapular fat pad weight		IAGP		N	RGD:5509061	20160616	MGI			PMID:24876128
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0011170	abnormal brown fat cell differentiation		IAGP		N	RGD:5509061	20160616	MGI			PMID:24876128
1557972	Taf7l	TATA-box binding protein associated factor 7 like	gene	MP:0011699	abnormal brown adipose tissue thermogenesis		IAGP		N	RGD:5509061	20160616	MGI			PMID:24876128
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20201022	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20201022	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20251113	MGI			PMID:35219498
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20220811	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20190502	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20251113	MGI			PMID:35219498
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20251113	MGI			PMID:35219498
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20190502	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20190502	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20220811	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0014372	decreased miniature excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20251113	MGI			PMID:35219498
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0014376	decreased miniature excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20251113	MGI			PMID:35219498
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20251113	MGI			PMID:35219498
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20251113	MGI			PMID:35219498
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0020422	decreased freezing behavior		IAGP		N	RGD:5509061	20251113	MGI			PMID:35219498
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1557973	Iqsec3	IQ motif and Sec7 domain 3	gene	MP:0031333	decreased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20251113	MGI			PMID:35219498
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20231207	MGI			
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20230601	MGI			
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20231207	MGI			
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21412262
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20151119	MGI			PMID:22716256
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20151119	MGI			PMID:22716256
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0003195	calcinosis		IAGP		N	RGD:5509061	20151119	MGI			PMID:22716256
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0005065	abnormal neutrophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0010178	increased number of Howell-Jolly bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0011176	abnormal erythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0012563	increased tumor incidence following infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0014993	erythrocyte maturation arrest		IAGP		N	RGD:5509061	20260514	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0020934	increased susceptibility to Retroviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:24029230
1557974	Samd9l	sterile alpha motif domain containing 9-like	gene	MP:0030025	giant platelets		IAGP		N	RGD:5509061	20170803	MGI			PMID:24029230
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751419
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0000727	absent CD8-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12065839
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388689
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10620608
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001759	increased urine glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285306
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:1910207
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1910207
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709807
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:10078545
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388689
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10078545
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751419
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751419
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10620608
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285306
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:2358682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11687799
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23712430
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11857806
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12198548
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002358	abnormal spleen periarteriolar lymphoid sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23772037
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285306
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12507777
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547694
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002454	abnormal macrophage antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547694
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23712430
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23772037
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547694
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2358682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1910207
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002726	abnormal pulmonary vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2358682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164958
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003410	abnormal artery development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17717295
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003504	thyroid gland inflammation		IEA		N	RGD:5509061	20111116	MGI			
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:2358682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751419
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12065839
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:22561606
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003790	absent CD4-positive, alpha-beta T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:23772037
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003888	liver hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751419
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003901	abnormal PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751419
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003944	abnormal T cell subpopulation ratio		IAGP		N	RGD:5509061	20180322	MGI			PMID:29472249
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547694
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8258349
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2358682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:2358682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004797	increased anti-erythrocyte antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388689
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23772037
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:10620608
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004803	increased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285306
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285306
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20180322	MGI			PMID:29472249
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004824	decreased susceptibility to experimental autoimmune myasthenia gravis		IAGP		N	RGD:5509061	20141003	MGI			PMID:3917973
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004918	abnormal negative T cell selection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19597498
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23712430
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005010	abnormal CD8-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285306
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:2358682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005025	abnormal response to infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653504
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164958
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9627126
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164958
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:2358682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:6948771
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005042	abnormal level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005090	increased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388689
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005122	increased circulating thyroid-stimulating hormone level		IEA		N	RGD:5509061	20111116	MGI			
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:10078545
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005351	decreased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20141003	MGI			PMID:12507777
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005355	enlarged thyroid gland		IEA		N	RGD:5509061	20111116	MGI			
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10620608
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285306
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:14525595
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751419
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0006045	mitral valve regurgitation		IAGP		N	RGD:5509061	20231221	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0006085	myocardium necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709807
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18258917
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388689
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164958
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082573
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1910207
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547694
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9885917
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20180322	MGI			PMID:29472249
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7547694
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17082573
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1910207
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20360383
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164958
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22561606
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8388689
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008397	abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709807
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008474	absent spleen germinal center		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9491996
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285306
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20260402	MGI			PMID:18258917
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19917682
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11285306
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:1909605
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21179499
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709807
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0010334	pleural effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14764740
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751419
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0010539	decreased level of surface class II molecules		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709807
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16709807
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0012765	decreased alpha-beta T cell number		IAGP		N	RGD:5509061	20180322	MGI			PMID:29472249
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0031712	torsade de pointes		IAGP		N	RGD:5509061	20260528	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0031756	first degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0031757	second degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0031760	Mobitz I atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:14570980
1557975	H2-Ab1	histocompatibility 2, class II antigen A, beta 1	gene	MP:0031762	third degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:14570980
1557976	Rapgef5	Rap guanine nucleotide exchange factor (GEF) 5	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20181227	MGI			
1557977	Rbp7	retinol binding protein 7, cellular	gene	MP:0011232	abnormal vitamin A level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15870066
1557978	Alpk2	alpha-kinase 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1557978	Alpk2	alpha-kinase 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20181227	MGI			
1557978	Alpk2	alpha-kinase 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20240523	MGI			
1557978	Alpk2	alpha-kinase 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1557978	Alpk2	alpha-kinase 2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0001362	abnormal anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15619115
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15753323
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:8662555
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15753323
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0001988	cocaine preference		IAGP		N	RGD:5509061	20141003	MGI			PMID:15753323
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15753323
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:8662555
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0008236	decreased susceptibility to neuronal excitotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24053122
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24053122
1557983	Grm2	glutamate receptor, metabotropic 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:15753323
1557984	Tcf23	transcription factor 23	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0002907	abnormal parturition		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0003566	abnormal cell adhesion		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0003845	abnormal decidualization		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0004514	dystocia		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0008256	abnormal myometrium morphology		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0008257	thin myometrium		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0009671	abnormal uterus physiology		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0012008	delayed parturition		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0012699	decreased maternal body weight gain		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0013258	abnormal extracellular matrix morphology		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557984	Tcf23	transcription factor 23	gene	MP:0020253	increased collagen level		IAGP		N	RGD:5509061	20241107	MGI			PMID:39014976
1557985	Trub2	TruB pseudouridine (psi) synthase family member 2	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1557985	Trub2	TruB pseudouridine (psi) synthase family member 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1557985	Trub2	TruB pseudouridine (psi) synthase family member 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1557985	Trub2	TruB pseudouridine (psi) synthase family member 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0000811	hippocampal neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028811
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028811
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0003690	abnormal glial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0006038	increased mitochondrial fission		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0008238	abnormal dorsoventral coat patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:18401429
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0010009	abnormal piriform cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028811
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028811
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22028811
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0014905	abnormal hepatocyte respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:22028811
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0014949	abnormal brain enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0014955	increased mitochondria enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0014956	decreased mitochondria enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:22914734
1557988	Uqcrfs1	ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	gene	MP:0020234	decreased basal metabolism		IAGP		N	RGD:5509061	20160421	MGI			PMID:22028811
1557990	Dazl	deleted in azoospermia-like	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288969
1557990	Dazl	deleted in azoospermia-like	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288969
1557990	Dazl	deleted in azoospermia-like	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514340
1557990	Dazl	deleted in azoospermia-like	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288969
1557990	Dazl	deleted in azoospermia-like	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288969
1557990	Dazl	deleted in azoospermia-like	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288969
1557990	Dazl	deleted in azoospermia-like	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11514340
1557990	Dazl	deleted in azoospermia-like	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288969
1557990	Dazl	deleted in azoospermia-like	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288969
1557990	Dazl	deleted in azoospermia-like	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288969
1557990	Dazl	deleted in azoospermia-like	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17219433
1557990	Dazl	deleted in azoospermia-like	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9288969
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000077	abnormal interparietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000106	abnormal basisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000109	abnormal parietal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000452	abnormal mouth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20171026	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326838
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0001890	anencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0002098	abnormal vibrissa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0002116	abnormal craniofacial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0002260	abnormal thyroid cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0003138	absent tympanic ring		IAGP		N	RGD:5509061	20171005	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0003235	abnormal alisphenoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0003800	monodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326838
1557991	Dlx6	distal-less homeobox 6	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004439	absent Meckel's cartilage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004452	abnormal pterygoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004453	abnormal pterygoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004594	abnormal mandibular coronoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004595	abnormal mandibular condyloid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20171019	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0005105	abnormal middle ear ossicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0005230	ectrodactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326838
1557991	Dlx6	distal-less homeobox 6	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0005274	abnormal viscerocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18326838
1557991	Dlx6	distal-less homeobox 6	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0008380	abnormal gonial bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0009917	abnormal hyoid bone body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0009918	abnormal stylohyoid ligament morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0010939	abnormal mandibular prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0010994	aerophagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12112878
1557991	Dlx6	distal-less homeobox 6	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0030259	mandibular condyloid process hypoplasia		IAGP		N	RGD:5509061	20171019	MGI			PMID:18697905
1557991	Dlx6	distal-less homeobox 6	gene	MP:0030299	lower jaw to upper jaw transformation		IAGP		N	RGD:5509061	20171102	MGI			PMID:12434331
1557991	Dlx6	distal-less homeobox 6	gene	MP:0030383	small presphenoid bone		IAGP		N	RGD:5509061	20171207	MGI			PMID:12434331
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000314	schistocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:658175
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0001585	hemolytic anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0001655	multifocal hepatic necrosis		IEA		N	RGD:5509061	20111116	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0001728	failure of embryo implantation		IEA		N	RGD:5509061	20240926	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6234993
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10772878
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002594	low mean erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002642	anisocytosis		IEA		N	RGD:5509061	20111116	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002643	poikilocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002704	tubular nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002812	spherocytosis		IEA		N	RGD:5509061	20111116	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002813	microcytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10772878
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20111116	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0003656	abnormal erythrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0003657	abnormal erythrocyte osmotic lysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20240926	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0004154	renal tubular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0005360	urolithiasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0008956	decreased cellular hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0010035	increased erythrocyte clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0010035	increased erythrocyte clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0010163	hemolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0010177	acanthocytosis		IEA		N	RGD:5509061	20111116	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0010375	increased kidney iron level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6234993
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:6763106
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20240926	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0011101	prenatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0011188	increased erythrocyte protoporphyrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:658175
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20240926	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220811	MGI			
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:10772878
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0020409	abnormal cardiac thrombosis		IAGP		N	RGD:5509061	20161124	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0021002	brain lesion		IAGP		N	RGD:5509061	20210805	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0021003	cerebral infarct		IAGP		N	RGD:5509061	20210805	MGI			PMID:9373273
1557994	Sptb	spectrin beta, erythrocytic	gene	MP:0031085	increased erythrocyte osmotic fragility		IAGP		N	RGD:5509061	20200716	MGI			PMID:9373273
1557995	Hoxb8	homeobox B8	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510925
1557995	Hoxb8	homeobox B8	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559485
1557995	Hoxb8	homeobox B8	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623233
1557995	Hoxb8	homeobox B8	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623233
1557995	Hoxb8	homeobox B8	gene	MP:0000155	asymmetric rib joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510925
1557995	Hoxb8	homeobox B8	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559485
1557995	Hoxb8	homeobox B8	gene	MP:0001077	abnormal spinal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559485
1557995	Hoxb8	homeobox B8	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779477
1557995	Hoxb8	homeobox B8	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559485
1557995	Hoxb8	homeobox B8	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510925
1557995	Hoxb8	homeobox B8	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559485
1557995	Hoxb8	homeobox B8	gene	MP:0001440	abnormal grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510925
1557995	Hoxb8	homeobox B8	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779477
1557995	Hoxb8	homeobox B8	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510925
1557995	Hoxb8	homeobox B8	gene	MP:0001501	abnormal sleep pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779477
1557995	Hoxb8	homeobox B8	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779477
1557995	Hoxb8	homeobox B8	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559485
1557995	Hoxb8	homeobox B8	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559485
1557995	Hoxb8	homeobox B8	gene	MP:0001973	increased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510925
1557995	Hoxb8	homeobox B8	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623233
1557995	Hoxb8	homeobox B8	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623233
1557995	Hoxb8	homeobox B8	gene	MP:0002114	abnormal axial skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11779477
1557995	Hoxb8	homeobox B8	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623233
1557995	Hoxb8	homeobox B8	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559485
1557995	Hoxb8	homeobox B8	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20510925
1557995	Hoxb8	homeobox B8	gene	MP:0008146	asymmetric sternocostal joints		IAGP		N	RGD:5509061	20141003	MGI			PMID:11311170
1557995	Hoxb8	homeobox B8	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559485
1557995	Hoxb8	homeobox B8	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623233
1557995	Hoxb8	homeobox B8	gene	MP:0012283	decreased sternebra number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623233
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0009729	absent tarsus bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0010714	iris coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12788935
1557997	Glce	glucuronyl C5-epimerase	gene	MP:0014473	increased pulmonary alveolus wall thickness		IAGP		N	RGD:5509061	20240704	MGI			PMID:12788935
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20200514	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20200310	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20200310	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0003929	decreased heart rate variability		IEA		N	RGD:5509061	20200514	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20260402	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20200310	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20200310	MGI			
1557998	Ppp2r2b	protein phosphatase 2, regulatory subunit B, beta	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1557999	Rnf216	ring finger protein 216	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20160421	MGI			
1557999	Rnf216	ring finger protein 216	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20190926	MGI			PMID:30649198
1557999	Rnf216	ring finger protein 216	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20190926	MGI			PMID:30649198
1557999	Rnf216	ring finger protein 216	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20190926	MGI			PMID:30649198
1557999	Rnf216	ring finger protein 216	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190926	MGI			PMID:30649198
1557999	Rnf216	ring finger protein 216	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0002631	abnormal epididymis morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:30649198
1557999	Rnf216	ring finger protein 216	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20190926	MGI			PMID:30649198
1557999	Rnf216	ring finger protein 216	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0004884	abnormal testis physiology		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30649198
1557999	Rnf216	ring finger protein 216	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210520	MGI			
1557999	Rnf216	ring finger protein 216	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20190926	MGI			PMID:30649198
1557999	Rnf216	ring finger protein 216	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1557999	Rnf216	ring finger protein 216	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20190926	MGI			PMID:30649198
1557999	Rnf216	ring finger protein 216	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:33724554
1557999	Rnf216	ring finger protein 216	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:30649198
1558000	Epb41l2	erythrocyte membrane protein band 4.1 like 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19225127
1558000	Epb41l2	erythrocyte membrane protein band 4.1 like 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19225127
1558000	Epb41l2	erythrocyte membrane protein band 4.1 like 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482674
1558000	Epb41l2	erythrocyte membrane protein band 4.1 like 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482674
1558000	Epb41l2	erythrocyte membrane protein band 4.1 like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482674
1558000	Epb41l2	erythrocyte membrane protein band 4.1 like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19225127
1558000	Epb41l2	erythrocyte membrane protein band 4.1 like 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482674
1558000	Epb41l2	erythrocyte membrane protein band 4.1 like 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482674
1558000	Epb41l2	erythrocyte membrane protein band 4.1 like 2	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21482674
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000065	abnormal bone marrow cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000075	absent neurocranium		IAGP		N	RGD:5509061	20171102	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000100	abnormal ethmoid bone morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000104	abnormal sphenoid bone morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000131	abnormal long bone epiphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000133	abnormal long bone metaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000141	abnormal vertebral body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000165	abnormal long bone hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20260402	MGI			
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20260402	MGI			
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000288	abnormal pericardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000602	dilated liver sinusoidal space		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20260402	MGI			
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20260402	MGI			
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20260402	MGI			
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873583
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22449950
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11802174
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22449950
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20260402	MGI			
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001290	delayed eyelid opening		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001636	irregular heartbeat		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002397	abnormal bone marrow morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002427	disproportionate dwarf		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002747	abnormal aortic valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002748	abnormal pulmonary valve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20260402	MGI			
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003279	aneurysm		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22449950
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004056	abnormal myocardium compact layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818570
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004134	abnormal chest morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004145	abnormal muscle electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004148	increased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004174	abnormal spine curvature		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16873583
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004373	bowed humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004376	absent frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004419	absent parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004669	enlarged vertebral body		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005229	abnormal intervertebral disk development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005269	abnormal occipital bone morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:22449950
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22449950
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514129
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0006397	disorganized long bone epiphyseal plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0008151	increased diameter of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0008160	increased diameter of humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0008272	abnormal endochondral bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:12814946
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:18647752
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0009459	skeletal muscle hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010426	abnormal heart and great artery attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818570
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010472	abnormal ascending aorta and coronary artery attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818570
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010584	abnormal conotruncus septation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010586	absent conotruncal ridges		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010588	conotruncal ridge hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12142349
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010732	abnormal node of Ranvier morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22449950
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010734	abnormal paranode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22449950
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010738	abnormal internode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22449950
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010742	increased Schwann cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22449950
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0010936	decreased airway resistance		IEA		N	RGD:5509061	20260402	MGI			
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0011238	abnormal inner ear development		IAGP		N	RGD:5509061	20240912	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0011514	skin hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0012175	flat face		IAGP		N	RGD:5509061	20141003	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0014101	decreased chondrocyte proliferation		IAGP		N	RGD:5509061	20171221	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0014516	abnormal middle ear development		IAGP		N	RGD:5509061	20240912	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20160609	MGI			PMID:10579729
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0020390	abnormal radial glial cell endfoot morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:16873583
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20171214	MGI			PMID:10545953
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0030788	abnormal femur head morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0030789	abnormal femur neck morphology		IAGP		N	RGD:5509061	20181011	MGI			PMID:17213231
1558001	Hspg2	perlecan (heparan sulfate proteoglycan 2)	gene	MP:0030793	short femur neck		IAGP		N	RGD:5509061	20181011	MGI			PMID:17213231
1558002	Rab19	RAB19, member RAS oncogene family	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20210826	MGI			
1558002	Rab19	RAB19, member RAS oncogene family	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1558002	Rab19	RAB19, member RAS oncogene family	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20240523	MGI			
1558002	Rab19	RAB19, member RAS oncogene family	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20210826	MGI			
1558002	Rab19	RAB19, member RAS oncogene family	gene	MP:0001469	abnormal contextual conditioning behavior		IEA		N	RGD:5509061	20211021	MGI			
1558002	Rab19	RAB19, member RAS oncogene family	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20160421	MGI			
1558002	Rab19	RAB19, member RAS oncogene family	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1558002	Rab19	RAB19, member RAS oncogene family	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20211021	MGI			
1558002	Rab19	RAB19, member RAS oncogene family	gene	MP:0012361	decreased large unstained cell number		IEA		N	RGD:5509061	20160421	MGI			
1558003	Zfp280c	zinc finger protein 280C	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20241121	MGI			
1558003	Zfp280c	zinc finger protein 280C	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1558003	Zfp280c	zinc finger protein 280C	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20240523	MGI			
1558003	Zfp280c	zinc finger protein 280C	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20241121	MGI			
1558003	Zfp280c	zinc finger protein 280C	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240718	MGI			PMID:35605119
1558003	Zfp280c	zinc finger protein 280C	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1558003	Zfp280c	zinc finger protein 280C	gene	MP:0012424	decreased alimentary system tumor incidence		IAGP		N	RGD:5509061	20240718	MGI			PMID:35605119
1558003	Zfp280c	zinc finger protein 280C	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20240718	MGI			PMID:35605119
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210128	MGI			
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20210128	MGI			
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0001192	scaly skin		IEA		N	RGD:5509061	20210128	MGI			
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0001384	abnormal pup retrieval		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0001447	abnormal nest building behavior		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210128	MGI			
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210128	MGI			
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0002557	abnormal social/conspecific interaction behavior		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0002885	abnormal AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210128	MGI			
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0004000	impaired passive avoidance behavior		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0020338	abnormal hippocampal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0020510	increased dendritic spine length		IAGP		N	RGD:5509061	20180208	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:28899869
1558006	Vrk3	vaccinia related kinase 3	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:28899869
1558007	Rfk	riboflavin kinase	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1558007	Rfk	riboflavin kinase	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230119	MGI			
1558007	Rfk	riboflavin kinase	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1558007	Rfk	riboflavin kinase	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20230119	MGI			
1558007	Rfk	riboflavin kinase	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20230119	MGI			
1558007	Rfk	riboflavin kinase	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230119	MGI			
1558007	Rfk	riboflavin kinase	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20230119	MGI			
1558007	Rfk	riboflavin kinase	gene	MP:0003604	single kidney		IEA		N	RGD:5509061	20230119	MGI			
1558007	Rfk	riboflavin kinase	gene	MP:0011077	decreased macrophage nitric oxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641494
1558007	Rfk	riboflavin kinase	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19641494
1558007	Rfk	riboflavin kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1558007	Rfk	riboflavin kinase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230119	MGI			
1558009	Asprv1	aspartic peptidase, retroviral-like 1	gene	MP:0001211	wrinkled skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16837463
1558009	Asprv1	aspartic peptidase, retroviral-like 1	gene	MP:0001510	abnormal coat appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16837463
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0013023	decreased Ly6C high monocyte number		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0013662	decreased myeloid cell number		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558011	Mospd2	motile sperm domain containing 2	gene	MP:0020212	impaired leukocyte migration		IAGP		N	RGD:5509061	20250918	MGI			PMID:32353176
1558012	Fgd1	FYVE, RhoGEF and PH domain containing 1	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20190502	MGI			
1558012	Fgd1	FYVE, RhoGEF and PH domain containing 1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1558012	Fgd1	FYVE, RhoGEF and PH domain containing 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210520	MGI			
1558012	Fgd1	FYVE, RhoGEF and PH domain containing 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190502	MGI			
1558012	Fgd1	FYVE, RhoGEF and PH domain containing 1	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1558012	Fgd1	FYVE, RhoGEF and PH domain containing 1	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1558013	Ogdh	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20211021	MGI			
1558013	Ogdh	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170504	MGI			
1558013	Ogdh	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1558013	Ogdh	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1558013	Ogdh	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20150430	MGI			
1558013	Ogdh	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20150430	MGI			
1558013	Ogdh	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1558013	Ogdh	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558013	Ogdh	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000046	abnormal sulcus ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000397	abnormal guard hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000402	abnormal zigzag hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000405	abnormal auchene hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000467	abnormal esophagus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015430
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000467	abnormal esophagus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000469	abnormal esophageal squamous epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015430
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982232
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000613	abnormal salivary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000762	abnormal tongue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015430
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000808	abnormal hippocampus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0000948	nonconvulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982232
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982232
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001288	abnormal lens induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882093
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20230223	MGI			PMID:23638914
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20220811	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001329	retina hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001395	bidirectional circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001675	abnormal ectoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514105
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514105
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029233
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001717	absent ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514105
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982232
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982232
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514105
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882093
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002067	abnormal sensory capabilities/reflexes/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:23153495
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882093
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982232
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20150205	MGI			PMID:21331042
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882093
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029233
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23918385
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002281	abnormal respiratory mucosa goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20011520
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002653	abnormal ependyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002697	abnormal eye size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0002984	retina hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003136	yellow coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003148	decreased cochlea coiling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003237	abnormal lens epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003240	loss of hippocampal neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003276	esophageal atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003300	gastrointestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982232
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003321	tracheoesophageal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003648	abnormal radial glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003817	abnormal pituitary diverticulum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20230601	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094324
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004317	small vestibular saccule		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004325	absent vestibular hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004336	small utricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004405	absent cochlear hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004416	absent cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004417	decreased cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004493	dilated cochlea		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21982232
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18638478
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0005128	decreased adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0005134	decreased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0005138	decreased prolactin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0005267	abnormal olfactory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15882093
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0005307	head tossing		IAGP		N	RGD:5509061	20141003	MGI			PMID:12036291
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0006071	abnormal retina progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0006089	abnormal vestibular saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15846349
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0006221	optic nerve hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16651659
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0006257	abnormal fungiform papillae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015430
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0006293	absent nasal placodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:17140559
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20011520
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20220811	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20141003	MGI			PMID:24209762
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008329	decreased somatotroph cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18638478
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0008794	increased lens epithelium apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19570848
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029233
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0009453	enhanced contextual conditioning behavior		IEA		N	RGD:5509061	20220519	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0009533	absent palatine gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0009534	absent anterior lingual gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20230223	MGI			PMID:23638914
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20230223	MGI			PMID:23638914
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20230223	MGI			PMID:23638914
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734891
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0010320	increased pituitary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24094324
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0010371	abnormal epiglottis morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0010863	absent respiratory mucosa goblet cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:20011520
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0010897	abnormal bronchiole epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20011520
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011054	absent respiratory motile cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20011520
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011071	absent club cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:20011520
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17015430
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17522155
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18638478
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029233
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12514105
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20170824	MGI			PMID:26658019
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15240551
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011184	absent embryonic epiblast		IAGP		N	RGD:5509061	20141003	MGI			PMID:23029233
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0013337	abnormal adenohypophysis development		IAGP		N	RGD:5509061	20141204	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0013342	bifurcated Rathke's pouch		IAGP		N	RGD:5509061	20141204	MGI			PMID:16932809
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0014236	increased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:29743593
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20230223	MGI			PMID:23638914
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0030129	tongue inflammation		IAGP		N	RGD:5509061	20171005	MGI			PMID:21982232
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0031278	decreased osteosarcoma incidence		IAGP		N	RGD:5509061	20230601	MGI			PMID:29743593
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:0031467	absent palatal taste bud		IAGP		N	RGD:5509061	20230615	MGI			PMID:17015430
1558014	Sox2	SRY (sex determining region Y)-box 2	gene	MP:3000003	abnormal Ebner's gland morphology		IAGP		N	RGD:5509061	20141225	MGI			PMID:17522155
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0005450	abnormal energy expenditure		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558016	Ankrd26	ankyrin repeat domain 26	gene	MP:0006094	increased fat cell size		IAGP		N	RGD:5509061	20160225	MGI			PMID:18162531
1558017	Cd207	CD207 antigen	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1558017	Cd207	CD207 antigen	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1558017	Cd207	CD207 antigen	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1558017	Cd207	CD207 antigen	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20180830	MGI			PMID:24638167
1558017	Cd207	CD207 antigen	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20180830	MGI			PMID:24638167
1558017	Cd207	CD207 antigen	gene	MP:0002534	abnormal type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998450
1558017	Cd207	CD207 antigen	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15897263
1558017	Cd207	CD207 antigen	gene	MP:0008117	abnormal Langerhans cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15601833
1558017	Cd207	CD207 antigen	gene	MP:0008117	abnormal Langerhans cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894281
1558017	Cd207	CD207 antigen	gene	MP:0008118	absent Langerhans cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894281
1558017	Cd207	CD207 antigen	gene	MP:0008118	absent Langerhans cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:15897263
1558017	Cd207	CD207 antigen	gene	MP:0008119	decreased Langerhans cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15894281
1558017	Cd207	CD207 antigen	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:24638167
1558017	Cd207	CD207 antigen	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18591406
1558017	Cd207	CD207 antigen	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21998450
1558017	Cd207	CD207 antigen	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1558017	Cd207	CD207 antigen	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1558017	Cd207	CD207 antigen	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1558017	Cd207	CD207 antigen	gene	MP:0020946	increased susceptibility to Orthomyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:18591406
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000270	abnormal heart tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0000926	absent floor plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0004214	abnormal long bone diaphysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0004252	abnormal direction of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0009743	preaxial polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16311594
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0011261	abnormal limb mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20920500
1558019	Ofd1	OFD1, centriole and centriolar satellite protein	gene	MP:0011682	renal glomerulus cyst		IAGP		N	RGD:5509061	20211021	MGI			PMID:16311594
1558020	Npsr1	neuropeptide S receptor 1	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1558020	Npsr1	neuropeptide S receptor 1	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:16829631
1558020	Npsr1	neuropeptide S receptor 1	gene	MP:0009453	enhanced contextual conditioning behavior		IAGP		N	RGD:5509061	20220623	MGI			PMID:31619542
1558020	Npsr1	neuropeptide S receptor 1	gene	MP:0010936	decreased airway resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16829631
1558020	Npsr1	neuropeptide S receptor 1	gene	MP:0012288	abnormal paradoxical sleep pattern		IAGP		N	RGD:5509061	20220623	MGI			PMID:31619542
1558020	Npsr1	neuropeptide S receptor 1	gene	MP:0012289	abnormal non-rapid eye movement sleep pattern		IAGP		N	RGD:5509061	20220623	MGI			PMID:31619542
1558020	Npsr1	neuropeptide S receptor 1	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20220623	MGI			PMID:31619542
1558020	Npsr1	neuropeptide S receptor 1	gene	MP:0020478	abnormal circadian sleep/wake cycle		IAGP		N	RGD:5509061	20220623	MGI			PMID:31619542
1558021	Jaml	junction adhesion molecule like	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
1558021	Jaml	junction adhesion molecule like	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
1558021	Jaml	junction adhesion molecule like	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
1558021	Jaml	junction adhesion molecule like	gene	MP:0005326	abnormal podocyte morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
1558021	Jaml	junction adhesion molecule like	gene	MP:0011282	increased podocyte apoptosis		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
1558021	Jaml	junction adhesion molecule like	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
1558021	Jaml	junction adhesion molecule like	gene	MP:0011561	renal glomerulus lipidosis		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
1558021	Jaml	junction adhesion molecule like	gene	MP:0011753	decreased podocyte number		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
1558021	Jaml	junction adhesion molecule like	gene	MP:0020153	abnormal urine albumin level		IAGP		N	RGD:5509061	20210304	MGI			PMID:33186558
1558022	Trappc2	trafficking protein particle complex 2	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210520	MGI			
1558022	Trappc2	trafficking protein particle complex 2	gene	MP:0005575	increased pulmonary ventilation		IEA		N	RGD:5509061	20210128	MGI			
1558022	Trappc2	trafficking protein particle complex 2	gene	MP:0005576	decreased pulmonary ventilation		IEA		N	RGD:5509061	20210128	MGI			
1558022	Trappc2	trafficking protein particle complex 2	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20170105	MGI			
1558022	Trappc2	trafficking protein particle complex 2	gene	MP:0012125	decreased bronchoconstrictive response		IEA		N	RGD:5509061	20250508	MGI			
1558023	Kbtbd11	kelch repeat and BTB (POZ) domain containing 11	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20200514	MGI			
1558023	Kbtbd11	kelch repeat and BTB (POZ) domain containing 11	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20200514	MGI			
1558023	Kbtbd11	kelch repeat and BTB (POZ) domain containing 11	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20200514	MGI			
1558023	Kbtbd11	kelch repeat and BTB (POZ) domain containing 11	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20200514	MGI			
1558023	Kbtbd11	kelch repeat and BTB (POZ) domain containing 11	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20200514	MGI			
1558023	Kbtbd11	kelch repeat and BTB (POZ) domain containing 11	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20200514	MGI			
1558023	Kbtbd11	kelch repeat and BTB (POZ) domain containing 11	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20200514	MGI			
1558023	Kbtbd11	kelch repeat and BTB (POZ) domain containing 11	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20220811	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20220811	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005344	increased circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008170	decreased B-1b cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008175	absent follicular B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423173
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0009923	decreased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558024	Atp11c	ATPase, class VI, type 11C	gene	MP:0010228	decreased transitional stage T3 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21423172
1558027	Hmx2	H6 homeobox 2	gene	MP:0000026	abnormal inner ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748138
1558027	Hmx2	H6 homeobox 2	gene	MP:0000034	abnormal inner ear vestibule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748138
1558027	Hmx2	H6 homeobox 2	gene	MP:0000036	absent semicircular canals		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748138
1558027	Hmx2	H6 homeobox 2	gene	MP:0000041	absent endolymphatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748138
1558027	Hmx2	H6 homeobox 2	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748138
1558027	Hmx2	H6 homeobox 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1558027	Hmx2	H6 homeobox 2	gene	MP:0002428	abnormal semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0002859	abnormal inner ear canal fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748138
1558027	Hmx2	H6 homeobox 2	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20170105	MGI			
1558027	Hmx2	H6 homeobox 2	gene	MP:0003069	abnormal superior semicircular canal morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0003162	decreased lateral semicircular canal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0003163	absent posterior semicircular canal		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20211021	MGI			
1558027	Hmx2	H6 homeobox 2	gene	MP:0003938	abnormal ear development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748138
1558027	Hmx2	H6 homeobox 2	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748138
1558027	Hmx2	H6 homeobox 2	gene	MP:0004249	abnormal crista ampullaris morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0004333	abnormal utricular macula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1558027	Hmx2	H6 homeobox 2	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:11748138
1558027	Hmx2	H6 homeobox 2	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20141003	MGI			PMID:15363417
1558027	Hmx2	H6 homeobox 2	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20170105	MGI			
1558027	Hmx2	H6 homeobox 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20260402	MGI			
1558027	Hmx2	H6 homeobox 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1558027	Hmx2	H6 homeobox 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1558030	Opn3	opsin 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1558030	Opn3	opsin 3	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1558030	Opn3	opsin 3	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1558030	Opn3	opsin 3	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0009132	abnormal white fat cell size		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0011014	decreased core body temperature		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0011973	abnormal circulating glycerol level		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558030	Opn3	opsin 3	gene	MP:0020325	abnormal beige fat cell morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:31968245
1558032	Hccs	holocytochrome c synthetase	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12444108
1558032	Hccs	holocytochrome c synthetase	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12444108
1558032	Hccs	holocytochrome c synthetase	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12444108
1558032	Hccs	holocytochrome c synthetase	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0003567	abnormal fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12444108
1558032	Hccs	holocytochrome c synthetase	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0010520	sinoatrial block		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0010636	bundle branch block		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12444108
1558032	Hccs	holocytochrome c synthetase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20240321	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0014072	decreased cardiac muscle glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0014906	abnormal muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0014908	decreased muscle cell respiration		IAGP		N	RGD:5509061	20260219	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0031607	abnormal fetal cardiomyocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0031608	decreased fetal cardiomyocyte size		IAGP		N	RGD:5509061	20240321	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0031756	first degree atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:18854137
1558032	Hccs	holocytochrome c synthetase	gene	MP:0031761	Mobitz II atrioventricular block		IAGP		N	RGD:5509061	20260806	MGI			PMID:18854137
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001417	decreased exploration in new environment		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0003243	abnormal dopaminergic neuron morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20180315	MGI			PMID:29112723
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20211021	MGI			
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20211021	MGI			
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20180315	MGI			PMID:29112723
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0012106	impaired exercise endurance		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20240215	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0014390	decreased myocardial fiber mitochondrial DNA content		IAGP		N	RGD:5509061	20240321	MGI			PMID:35700042
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0014694	anisokaryosis		IAGP		N	RGD:5509061	20250710	MGI			PMID:30877432
1558033	Chchd10	coiled-coil-helix-coiled-coil-helix domain containing 10	gene	MP:0020851	abnormal vacuole morphology		IAGP		N	RGD:5509061	20190411	MGI			PMID:30877432
1558034	Rint1	RAD50 interactor 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20220811	MGI			
1558034	Rint1	RAD50 interactor 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0002014	increased papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0002041	increased pituitary adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20220811	MGI			
1558034	Rint1	RAD50 interactor 1	gene	MP:0002947	increased hemangioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0003570	increased uterus leiomyoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1558034	Rint1	RAD50 interactor 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220811	MGI			
1558034	Rint1	RAD50 interactor 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1558034	Rint1	RAD50 interactor 1	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20220811	MGI			
1558034	Rint1	RAD50 interactor 1	gene	MP:0008000	increased ovary tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0009687	empty decidua capsularis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0009704	increased skin squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0010309	increased mesothelioma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558034	Rint1	RAD50 interactor 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1558034	Rint1	RAD50 interactor 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1558034	Rint1	RAD50 interactor 1	gene	MP:0013488	increased keratoacanthoma incidence		IAGP		N	RGD:5509061	20150212	MGI			PMID:17470549
1558034	Rint1	RAD50 interactor 1	gene	MP:0013751	increased cystadenoma incidence		IAGP		N	RGD:5509061	20150416	MGI			PMID:17470549
1558038	Sec14l1	SEC14-like lipid binding 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1558038	Sec14l1	SEC14-like lipid binding 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1558040	Cd96	CD96 antigen	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1558040	Cd96	CD96 antigen	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20191219	MGI			PMID:24658051
1558040	Cd96	CD96 antigen	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20190425	MGI			PMID:24658051
1558040	Cd96	CD96 antigen	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20191219	MGI			PMID:24658051
1558040	Cd96	CD96 antigen	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20191219	MGI			PMID:24658051
1558040	Cd96	CD96 antigen	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20190425	MGI			PMID:24658051
1558041	Dab1	disabled 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1558041	Dab1	disabled 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0000746	weakness		IEA		N	RGD:5509061	20141003	MGI			
1558041	Dab1	disabled 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249135
1558041	Dab1	disabled 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11830577
1558041	Dab1	disabled 1	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249135
1558041	Dab1	disabled 1	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1558041	Dab1	disabled 1	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1558041	Dab1	disabled 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249135
1558041	Dab1	disabled 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11830577
1558041	Dab1	disabled 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17182786
1558041	Dab1	disabled 1	gene	MP:0000819	abnormal olfactory bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17494763
1558041	Dab1	disabled 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0000851	cerebellum hypoplasia		IEA		N	RGD:5509061	20111116	MGI			
1558041	Dab1	disabled 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18029196
1558041	Dab1	disabled 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0000853	absent cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1558041	Dab1	disabled 1	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18029196
1558041	Dab1	disabled 1	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18029196
1558041	Dab1	disabled 1	gene	MP:0000875	abnormal cerebellar Purkinje cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:18029196
1558041	Dab1	disabled 1	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1558041	Dab1	disabled 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0001391	abnormal tail movements		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18029196
1558041	Dab1	disabled 1	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1558041	Dab1	disabled 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20111116	MGI			
1558041	Dab1	disabled 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18029196
1558041	Dab1	disabled 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15249135
1558041	Dab1	disabled 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1558041	Dab1	disabled 1	gene	MP:0002397	abnormal bone marrow morphology		IEA		N	RGD:5509061	20111116	MGI			
1558041	Dab1	disabled 1	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18029196
1558041	Dab1	disabled 1	gene	MP:0003644	thymus atrophy		IEA		N	RGD:5509061	20111116	MGI			
1558041	Dab1	disabled 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11580894
1558041	Dab1	disabled 1	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11580894
1558041	Dab1	disabled 1	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11580894
1558041	Dab1	disabled 1	gene	MP:0004275	abnormal postnatal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17494763
1558041	Dab1	disabled 1	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17494763
1558041	Dab1	disabled 1	gene	MP:0005150	cachexia		IEA		N	RGD:5509061	20111116	MGI			
1558041	Dab1	disabled 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11830577
1558041	Dab1	disabled 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1558041	Dab1	disabled 1	gene	MP:0006074	abnormal retina rod bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11580894
1558041	Dab1	disabled 1	gene	MP:0008265	abnormal hippocampus CA2 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11830577
1558041	Dab1	disabled 1	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24210661
1558041	Dab1	disabled 1	gene	MP:0008440	abnormal subplate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0008443	absent subplate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1558041	Dab1	disabled 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21315259
1558041	Dab1	disabled 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0009940	abnormal hippocampus pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8875886
1558041	Dab1	disabled 1	gene	MP:0009949	abnormal olfactory bulb granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17494763
1558041	Dab1	disabled 1	gene	MP:0009956	abnormal cerebellar layer morphology		IEA		N	RGD:5509061	20141003	MGI			
1558041	Dab1	disabled 1	gene	MP:0011083	lethality at weaning, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1558041	Dab1	disabled 1	gene	MP:0011085	postnatal lethality, complete penetrance		IEA		N	RGD:5509061	20141003	MGI			
1558041	Dab1	disabled 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1558041	Dab1	disabled 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1558041	Dab1	disabled 1	gene	MP:0013138	thin body		IEA		N	RGD:5509061	20141003	MGI			
1558041	Dab1	disabled 1	gene	MP:0015022	disorganized cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0015023	inverted cerebral cortex lamination		IAGP		N	RGD:5509061	20260709	MGI			PMID:18981215
1558041	Dab1	disabled 1	gene	MP:0015049	disorganized cerebellar granule layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:10959835
1558041	Dab1	disabled 1	gene	MP:0030956	abnormal neuronal precursor cell migration		IAGP		N	RGD:5509061	20190725	MGI			PMID:17494763
1558042	Efhb	EF hand domain family, member B	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1558042	Efhb	EF hand domain family, member B	gene	MP:0010506	prolonged RR interval		IEA		N	RGD:5509061	20211021	MGI			
1558043	Lrch1	leucine-rich repeats and calponin homology (CH) domain containing 1	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180329	MGI			PMID:28028151
1558043	Lrch1	leucine-rich repeats and calponin homology (CH) domain containing 1	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20180329	MGI			PMID:28028151
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210805	MGI			
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210805	MGI			
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210805	MGI			
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20221215	MGI			
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0008639	decreased circulating interleukin-1 alpha level		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558044	Slc6a14	solute carrier family 6 (neurotransmitter transporter), member 14	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20161201	MGI			PMID:26173258
1558045	Slamf6	SLAM family member 6	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1558045	Slamf6	SLAM family member 6	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558045	Slamf6	SLAM family member 6	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558045	Slamf6	SLAM family member 6	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558045	Slamf6	SLAM family member 6	gene	MP:0005074	impaired granulocyte bactericidal activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558045	Slamf6	SLAM family member 6	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558045	Slamf6	SLAM family member 6	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558045	Slamf6	SLAM family member 6	gene	MP:0008632	increased circulating interleukin-16 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558045	Slamf6	SLAM family member 6	gene	MP:0008647	increased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558045	Slamf6	SLAM family member 6	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558045	Slamf6	SLAM family member 6	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15879084
1558047	Agbl3	ATP/GTP binding protein-like 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150122	MGI			PMID:25103237
1558048	Sema4c	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C	gene	MP:0000373	belly spot		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1558048	Sema4c	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C	gene	MP:0000886	abnormal cerebellar granule layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1558048	Sema4c	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1558048	Sema4c	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1558048	Sema4c	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C	gene	MP:0009964	abnormal cerebellum lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1558048	Sema4c	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1558048	Sema4c	sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21122816
1558050	Uqcrq	ubiquinol-cytochrome c reductase, complex III subunit VII	gene	MP:0008935	decreased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1558050	Uqcrq	ubiquinol-cytochrome c reductase, complex III subunit VII	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558050	Uqcrq	ubiquinol-cytochrome c reductase, complex III subunit VII	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1558051	Galntl5	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24398516
1558051	Galntl5	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24398516
1558051	Galntl5	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24398516
1558051	Galntl5	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24398516
1558051	Galntl5	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24398516
1558051	Galntl5	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24398516
1558051	Galntl5	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5	gene	MP:0011959	abnormal eye posterior chamber depth		IEA		N	RGD:5509061	20220811	MGI			
1558053	Morc4	microrchidia 4	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1558053	Morc4	microrchidia 4	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210128	MGI			
1558053	Morc4	microrchidia 4	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1558053	Morc4	microrchidia 4	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210128	MGI			
1558053	Morc4	microrchidia 4	gene	MP:0003900	shortened QT interval		IEA		N	RGD:5509061	20230601	MGI			
1558053	Morc4	microrchidia 4	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1558054	Acot3	acyl-CoA thioesterase 3	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20201022	MGI			
1558054	Acot3	acyl-CoA thioesterase 3	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220519	MGI			
1558054	Acot3	acyl-CoA thioesterase 3	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20201022	MGI			
1558054	Acot3	acyl-CoA thioesterase 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1558054	Acot3	acyl-CoA thioesterase 3	gene	MP:0003068	enlarged kidney		IEA		N	RGD:5509061	20210826	MGI			
1558056	Lcn12	lipocalin 12	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20250508	MGI			
1558056	Lcn12	lipocalin 12	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1558057	Parn	poly(A)-specific ribonuclease (deadenylation nuclease)	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200430	MGI			PMID:31273937
1558059	Hmces	5-hydroxymethylcytosine (hmC) binding, ES cell specific	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20180524	MGI			PMID:29020633
1558059	Hmces	5-hydroxymethylcytosine (hmC) binding, ES cell specific	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180524	MGI			PMID:29020633
1558059	Hmces	5-hydroxymethylcytosine (hmC) binding, ES cell specific	gene	MP:0008877	abnormal DNA methylation		IAGP		N	RGD:5509061	20180524	MGI			PMID:29020633
1558059	Hmces	5-hydroxymethylcytosine (hmC) binding, ES cell specific	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180524	MGI			PMID:29020633
1558059	Hmces	5-hydroxymethylcytosine (hmC) binding, ES cell specific	gene	MP:0011104	embryonic lethality before implantation, incomplete penetrance		IAGP		N	RGD:5509061	20180524	MGI			PMID:29020633
1558059	Hmces	5-hydroxymethylcytosine (hmC) binding, ES cell specific	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20180524	MGI			PMID:29020633
1558060	Hoxa11	homeobox A11	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902826
1558060	Hoxa11	homeobox A11	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0000521	abnormal kidney cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0000524	decreased renal tubule number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493536
1558060	Hoxa11	homeobox A11	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902826
1558060	Hoxa11	homeobox A11	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250683
1558060	Hoxa11	homeobox A11	gene	MP:0000552	abnormal radius morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521905
1558060	Hoxa11	homeobox A11	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250683
1558060	Hoxa11	homeobox A11	gene	MP:0000555	absent carpal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902826
1558060	Hoxa11	homeobox A11	gene	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521905
1558060	Hoxa11	homeobox A11	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0001539	decreased caudal vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217321
1558060	Hoxa11	homeobox A11	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217321
1558060	Hoxa11	homeobox A11	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18942146
1558060	Hoxa11	homeobox A11	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217321
1558060	Hoxa11	homeobox A11	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:18942146
1558060	Hoxa11	homeobox A11	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493536
1558060	Hoxa11	homeobox A11	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0002160	abnormal reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20260219	MGI			PMID:40389054
1558060	Hoxa11	homeobox A11	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902826
1558060	Hoxa11	homeobox A11	gene	MP:0002187	abnormal fibula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521905
1558060	Hoxa11	homeobox A11	gene	MP:0002286	cryptorchism		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0002769	abnormal vas deferens morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250683
1558060	Hoxa11	homeobox A11	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1558060	Hoxa11	homeobox A11	gene	MP:0003050	abnormal sacral vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902826
1558060	Hoxa11	homeobox A11	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0003446	renal hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0003600	ectopic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0003613	abnormal kidney medulla development		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0003626	kidney medulla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493536
1558060	Hoxa11	homeobox A11	gene	MP:0003672	abnormal ureter development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1558060	Hoxa11	homeobox A11	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0003857	abnormal hindlimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1558060	Hoxa11	homeobox A11	gene	MP:0004014	abnormal uterine environment		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217321
1558060	Hoxa11	homeobox A11	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217321
1558060	Hoxa11	homeobox A11	gene	MP:0004360	absent ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0004509	abnormal pelvic girdle bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1558060	Hoxa11	homeobox A11	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1558060	Hoxa11	homeobox A11	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558060	Hoxa11	homeobox A11	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902826
1558060	Hoxa11	homeobox A11	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0004649	decreased sacral vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0004650	increased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217321
1558060	Hoxa11	homeobox A11	gene	MP:0004650	increased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0004650	increased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902826
1558060	Hoxa11	homeobox A11	gene	MP:0004650	increased lumbar vertebrae number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250683
1558060	Hoxa11	homeobox A11	gene	MP:0004656	absent sacral vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12869760
1558060	Hoxa11	homeobox A11	gene	MP:0004896	abnormal endometrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493536
1558060	Hoxa11	homeobox A11	gene	MP:0005104	abnormal tarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902826
1558060	Hoxa11	homeobox A11	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250683
1558060	Hoxa11	homeobox A11	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521905
1558060	Hoxa11	homeobox A11	gene	MP:0005109	abnormal talus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0008159	increased diameter of fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493536
1558060	Hoxa11	homeobox A11	gene	MP:0008159	increased diameter of fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521905
1558060	Hoxa11	homeobox A11	gene	MP:0008161	increased diameter of radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217321
1558060	Hoxa11	homeobox A11	gene	MP:0008161	increased diameter of radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521905
1558060	Hoxa11	homeobox A11	gene	MP:0008162	increased diameter of tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521905
1558060	Hoxa11	homeobox A11	gene	MP:0008163	increased diameter of ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217321
1558060	Hoxa11	homeobox A11	gene	MP:0008163	increased diameter of ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:9521905
1558060	Hoxa11	homeobox A11	gene	MP:0008258	thin endometrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:12217321
1558060	Hoxa11	homeobox A11	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:7902826
1558060	Hoxa11	homeobox A11	gene	MP:0008915	fused carpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9250683
1558060	Hoxa11	homeobox A11	gene	MP:0009096	decreased endometrial gland number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0009097	absent endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0009214	vas deferens hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0009728	abnormal calcaneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0010978	absent ureteric bud		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0010984	abnormal metanephric mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493536
1558060	Hoxa11	homeobox A11	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11688568
1558060	Hoxa11	homeobox A11	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0011366	absent metanephros		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12050119
1558060	Hoxa11	homeobox A11	gene	MP:0011565	kidney papillary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7596412
1558060	Hoxa11	homeobox A11	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:7789268
1558060	Hoxa11	homeobox A11	gene	MP:0014320	abnormal autopod rotation		IAGP		N	RGD:5509061	20240404	MGI			PMID:7596412
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20201022	MGI			
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20160421	MGI			
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20160421	MGI			
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20230601	MGI			
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0003894	abnormal Purkinje cell innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160421	MGI			
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20170105	MGI			
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20210128	MGI			
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0011268	biphasic excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558061	Sez6l	seizure related 6 homolog like	gene	MP:0011272	short excitatory postsynaptic current rise time		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965762
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10662643
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367153
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000853	absent cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10662643
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000853	absent cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000853	absent cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367153
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10662643
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965762
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367153
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000873	thin external granule cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965762
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000874	irregular external granule cell layer thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965762
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878293
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10662643
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367153
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10662643
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367153
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20241121	MGI			PMID:17878293
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965762
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24717433
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0002622	abnormal cochlear hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0002623	abnormal vestibular hair cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:24717433
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0003247	abnormal glutaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439493
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004325	absent vestibular hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364557
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004405	absent cochlear hair cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10364557
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12441305
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004529	decreased outer hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004534	decreased inner hair cell stereocilia number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17570220
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19965762
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914183
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0006108	abnormal hindbrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16202705
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17570220
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10662643
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17570220
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19914183
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20533400
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9367153
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:24265785
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0012490	abnormal cochlear VIII nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19439493
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0014076	absent Paneth cells		IAGP		N	RGD:5509061	20250320	MGI			PMID:31442404
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20161013	MGI			PMID:19965762
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:10662643
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0015048	disorganized cerebellar Purkinje cell layer		IAGP		N	RGD:5509061	20260813	MGI			PMID:9367153
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20161117	MGI			PMID:19965762
1558062	Atoh1	atonal bHLH transcription factor 1	gene	MP:0031319	impaired intestine regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:17570220
1558064	Exph5	exophilin 5	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20210128	MGI			
1558064	Exph5	exophilin 5	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1558064	Exph5	exophilin 5	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20260402	MGI			
1558064	Exph5	exophilin 5	gene	MP:0001952	increased airway responsiveness		IAGP		N	RGD:5509061	20211202	MGI			PMID:32240120
1558064	Exph5	exophilin 5	gene	MP:0002944	increased lactate dehydrogenase level		IAGP		N	RGD:5509061	20211202	MGI			PMID:32240120
1558064	Exph5	exophilin 5	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20211202	MGI			PMID:32240120
1558064	Exph5	exophilin 5	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1558064	Exph5	exophilin 5	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20211202	MGI			PMID:32240120
1558064	Exph5	exophilin 5	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20210128	MGI			
1558064	Exph5	exophilin 5	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20211202	MGI			PMID:32240120
1558064	Exph5	exophilin 5	gene	MP:0005628	decreased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1558064	Exph5	exophilin 5	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:32240120
1558064	Exph5	exophilin 5	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:32240120
1558064	Exph5	exophilin 5	gene	MP:0008702	increased interleukin-5 secretion		IAGP		N	RGD:5509061	20211202	MGI			PMID:32240120
1558064	Exph5	exophilin 5	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20151203	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0000273	overriding aortic valve		IEA		N	RGD:5509061	20151203	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210520	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0001512	trunk curl		IEA		N	RGD:5509061	20201022	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0001625	cardiac hypertrophy		IEA		N	RGD:5509061	20141003	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0006061	right atrial isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20201022	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0010420	muscular ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0010476	coronary fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0010854	lung situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011250	abdominal situs ambiguus		IEA		N	RGD:5509061	20151203	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011252	situs inversus totalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011649	immotile respiratory cilia		IEA		N	RGD:5509061	20141003	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011665	d-loop transposition of the great arteries		IEA		N	RGD:5509061	20151203	MGI			
1558065	Dnaaf4	dynein axonemal assembly factor 4	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:23872636
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000108	midline facial cleft		IAGP		N	RGD:5509061	20160128	MGI			PMID:21515572
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000288	abnormal pericardium morphology		IEA		N	RGD:5509061	20201022	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20210128	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20160128	MGI			PMID:21515572
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262862
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000919	cranioschisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262862
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0001614	abnormal blood vessel morphology		IEA		N	RGD:5509061	20210128	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20210128	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0002109	abnormal limb morphology		IEA		N	RGD:5509061	20210128	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262862
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262862
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20201022	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003257	abnormal abdominal wall morphology		IEA		N	RGD:5509061	20210128	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003385	abnormal body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003425	abnormal optic vesicle formation		IEA		N	RGD:5509061	20201022	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262862
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003864	abnormal midbrain development		IEA		N	RGD:5509061	20201022	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20241121	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0004320	split sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0004391	abnormal respiratory conducting tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0004604	abnormal vertebral pedicle morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0004838	abnormal neural fold elevation formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0006108	abnormal hindbrain development		IEA		N	RGD:5509061	20200514	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262862
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0010831	lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0010976	small lung lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262862
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20210128	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0012260	encephalomeningocele		IAGP		N	RGD:5509061	20160128	MGI			PMID:21515572
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0012544	abnormal caudal neuropore morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21262862
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0012686	everted embryonic neuroepithelium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20654612
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0012707	incomplete caudal neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978075
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20170928	MGI			PMID:21377456
1558066	Grhl2	grainyhead like transcription factor 2	gene	MP:0030579	thoracoabdominoschisis		IAGP		N	RGD:5509061	20180607	MGI			PMID:21377456
1558067	Lrriq1	leucine-rich repeats and IQ motif containing 1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20240905	MGI			PMID:36129630
1558067	Lrriq1	leucine-rich repeats and IQ motif containing 1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20240905	MGI			PMID:36129630
1558067	Lrriq1	leucine-rich repeats and IQ motif containing 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20240905	MGI			PMID:36129630
1558068	Unc5cl	unc-5 family C-terminal like	gene	MP:0001126	abnormal ovary morphology		IEA		N	RGD:5509061	20210826	MGI			
1558068	Unc5cl	unc-5 family C-terminal like	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1558068	Unc5cl	unc-5 family C-terminal like	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1558068	Unc5cl	unc-5 family C-terminal like	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1558068	Unc5cl	unc-5 family C-terminal like	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1558068	Unc5cl	unc-5 family C-terminal like	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1558068	Unc5cl	unc-5 family C-terminal like	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20210520	MGI			
1558069	Hspa1a	heat shock protein family A (Hsp70) member 1A	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713291
1558069	Hspa1a	heat shock protein family A (Hsp70) member 1A	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:11713291
1558070	Siva1	SIVA1, apoptosis-inducing factor	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1558070	Siva1	SIVA1, apoptosis-inducing factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150910	MGI			PMID:25813352
1558070	Siva1	SIVA1, apoptosis-inducing factor	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20150910	MGI			PMID:25813352
1558070	Siva1	SIVA1, apoptosis-inducing factor	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20150910	MGI			PMID:25813352
1558070	Siva1	SIVA1, apoptosis-inducing factor	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:25813352
1558070	Siva1	SIVA1, apoptosis-inducing factor	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1558070	Siva1	SIVA1, apoptosis-inducing factor	gene	MP:0020190	abnormal lung adenoma incidence		IAGP		N	RGD:5509061	20150910	MGI			PMID:25813352
1558071	Mbnl3	muscleblind like splicing factor 3	gene	MP:0009400	decreased skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23660517
1558071	Mbnl3	muscleblind like splicing factor 3	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23660517
1558071	Mbnl3	muscleblind like splicing factor 3	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:23660517
1558071	Mbnl3	muscleblind like splicing factor 3	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20211125	MGI			PMID:23660517
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051870
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051870
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051870
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051870
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640454
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051870
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640454
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001701	incomplete embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001712	abnormal placenta development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001713	decreased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640454
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051870
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640454
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0002584	small ectoplacental cone		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759306
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15051870
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0003403	absent placental labyrinth		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0003491	abnormal voluntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759306
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640454
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640454
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0004560	abnormal chorionic plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759306
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0005033	abnormal trophoblast giant cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759306
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0009656	delayed chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0009658	increased placenta apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0009683	abnormal lateral corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759306
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640454
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12640454
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14749382
1558075	Pnpla6	patatin-like phospholipase domain containing 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:12640454
1558077	Ankrd28	ankyrin repeat domain 28	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20240523	MGI			
1558077	Ankrd28	ankyrin repeat domain 28	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1558077	Ankrd28	ankyrin repeat domain 28	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20240523	MGI			
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0000890	thin cerebellar molecular layer		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0001407	short stride length		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509342
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509342
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509342
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509342
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0009719	reduced cerebellar foliation		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0010008	abnormal Purkinje cell migration		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19509342
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170302	MGI			PMID:26035387
1558078	Sun2	Sad1 and UNC84 domain containing 2	gene	MP:0012362	increased large unstained cell number		IEA		N	RGD:5509061	20211021	MGI			
1558079	Htatsf1	HIV TAT specific factor 1	gene	MP:0002399	abnormal pluripotent precursor cell morphology		IAGP		N	RGD:5509061	20191017	MGI			PMID:29625069
1558080	Zdhhc15	zinc finger, DHHC domain containing 15	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20111116	MGI			
1558080	Zdhhc15	zinc finger, DHHC domain containing 15	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20111116	MGI			
1558082	Flnc	filamin C, gamma	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1558082	Flnc	filamin C, gamma	gene	MP:0000269	abnormal heart looping		IEA		N	RGD:5509061	20201022	MGI			
1558082	Flnc	filamin C, gamma	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20250508	MGI			
1558082	Flnc	filamin C, gamma	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20170831	MGI			PMID:26472074
1558082	Flnc	filamin C, gamma	gene	MP:0001691	abnormal somite shape		IEA		N	RGD:5509061	20201022	MGI			
1558082	Flnc	filamin C, gamma	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20170831	MGI			PMID:26472074
1558082	Flnc	filamin C, gamma	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0003083	abnormal tibialis anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0003229	abnormal vitelline vasculature morphology		IEA		N	RGD:5509061	20201022	MGI			
1558082	Flnc	filamin C, gamma	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:26472074
1558082	Flnc	filamin C, gamma	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:26472074
1558082	Flnc	filamin C, gamma	gene	MP:0004091	abnormal Z line morphology		IAGP		N	RGD:5509061	20170831	MGI			PMID:26472074
1558082	Flnc	filamin C, gamma	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0004246	abnormal extensor digitorum longus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0005534	decreased body temperature		IEA		N	RGD:5509061	20240523	MGI			
1558082	Flnc	filamin C, gamma	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0009412	skeletal muscle fiber degeneration		IAGP		N	RGD:5509061	20170831	MGI			PMID:26472074
1558082	Flnc	filamin C, gamma	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20170831	MGI			PMID:26472074
1558082	Flnc	filamin C, gamma	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20170831	MGI			PMID:26472074
1558082	Flnc	filamin C, gamma	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16914736
1558082	Flnc	filamin C, gamma	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558082	Flnc	filamin C, gamma	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20170831	MGI			PMID:26472074
1558082	Flnc	filamin C, gamma	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1558084	Rasal2	RAS protein activator like 2	gene	MP:0001272	increased metastatic potential		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20201022	MGI			
1558084	Rasal2	RAS protein activator like 2	gene	MP:0001883	increased mammary adenocarcinoma incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0002044	increased colon adenoma incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0002073	abnormal hair growth		IEA		N	RGD:5509061	20201022	MGI			
1558084	Rasal2	RAS protein activator like 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0003750	increased mouth tumor incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0006358	absent pinna reflex		IEA		N	RGD:5509061	20170105	MGI			
1558084	Rasal2	RAS protein activator like 2	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20160225	MGI			PMID:24029233
1558084	Rasal2	RAS protein activator like 2	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:24029233
1558085	Zmat4	zinc finger, matrin type 4	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20220811	MGI			
1558087	Cbx8	chromobox 8	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22094252
1558088	Map7d2	MAP7 domain containing 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16219627
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14583446
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16219627
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16219627
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0003172	abnormal lysosome physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14583446
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16219627
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:16219627
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16219627
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0005059	lysosomal protein accumulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17498992
1558089	Galns	galactosamine (N-acetyl)-6-sulfatase	gene	MP:0011473	increased urine glycosaminoglycan level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14583446
1558090	Hdac8	histone deacetylase 8	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1558090	Hdac8	histone deacetylase 8	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1558090	Hdac8	histone deacetylase 8	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20211230	MGI			PMID:30620721
1558090	Hdac8	histone deacetylase 8	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20160804	MGI			
1558090	Hdac8	histone deacetylase 8	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1558090	Hdac8	histone deacetylase 8	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20211230	MGI			PMID:30620721
1558090	Hdac8	histone deacetylase 8	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20211230	MGI			PMID:30620721
1558090	Hdac8	histone deacetylase 8	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20211230	MGI			PMID:30620721
1558090	Hdac8	histone deacetylase 8	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1558090	Hdac8	histone deacetylase 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1558090	Hdac8	histone deacetylase 8	gene	MP:0003121	genetic imprinting		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1558090	Hdac8	histone deacetylase 8	gene	MP:0004023	abnormal chromosome number		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1558090	Hdac8	histone deacetylase 8	gene	MP:0004378	frontal bone foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1558090	Hdac8	histone deacetylase 8	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1558090	Hdac8	histone deacetylase 8	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20211230	MGI			PMID:30620721
1558090	Hdac8	histone deacetylase 8	gene	MP:0008276	failure of intramembranous bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1558090	Hdac8	histone deacetylase 8	gene	MP:0008957	abnormal placenta junctional zone morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1558090	Hdac8	histone deacetylase 8	gene	MP:0008959	abnormal spongiotrophoblast cell morphology		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1558090	Hdac8	histone deacetylase 8	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1558090	Hdac8	histone deacetylase 8	gene	MP:0009429	decreased embryo weight		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1558090	Hdac8	histone deacetylase 8	gene	MP:0010038	abnormal placenta physiology		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1558090	Hdac8	histone deacetylase 8	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20141003	MGI			
1558090	Hdac8	histone deacetylase 8	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230629	MGI			PMID:32800293
1558090	Hdac8	histone deacetylase 8	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1558090	Hdac8	histone deacetylase 8	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19605684
1558090	Hdac8	histone deacetylase 8	gene	MP:0014321	short forelimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:32800293
1558090	Hdac8	histone deacetylase 8	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:32800293
1558092	Arf3	ARF GTPase 3	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1558092	Arf3	ARF GTPase 3	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220811	MGI			
1558092	Arf3	ARF GTPase 3	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1558092	Arf3	ARF GTPase 3	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1558092	Arf3	ARF GTPase 3	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1558092	Arf3	ARF GTPase 3	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20260402	MGI			
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20160811	MGI			
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0000462	abnormal digestive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803964
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803964
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803964
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0003722	absent ureter		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803964
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0004539	absent maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803964
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0005505	thrombocytosis		IEA		N	RGD:5509061	20210128	MGI			
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0010983	abnormal ureteric bud invasion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803964
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15148409
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0011364	abnormal metanephros morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803964
1558093	Ctnnbip1	catenin beta interacting protein 1	gene	MP:0011386	increased metanephric mesenchyme apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17803964
1558094	Gabpb2	GA repeat binding protein, beta 2	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20241121	MGI			
1558094	Gabpb2	GA repeat binding protein, beta 2	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628204
1558094	Gabpb2	GA repeat binding protein, beta 2	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1558094	Gabpb2	GA repeat binding protein, beta 2	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628204
1558094	Gabpb2	GA repeat binding protein, beta 2	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20241121	MGI			
1558094	Gabpb2	GA repeat binding protein, beta 2	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628204
1558094	Gabpb2	GA repeat binding protein, beta 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18628204
1558094	Gabpb2	GA repeat binding protein, beta 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0003443	increased circulating glycerol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0003975	increased circulating VLDL triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0005145	increased circulating VLDL cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0008963	increased carbon dioxide production		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0008965	increased basal metabolism		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0009293	decreased inguinal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558095	C1qtnf2	C1q and tumor necrosis factor related protein 2	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439668
1558096	Dnajc24	DnaJ heat shock protein family (Hsp40) member C24	gene	MP:0000562	polydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765564
1558096	Dnajc24	DnaJ heat shock protein family (Hsp40) member C24	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765564
1558096	Dnajc24	DnaJ heat shock protein family (Hsp40) member C24	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765564
1558096	Dnajc24	DnaJ heat shock protein family (Hsp40) member C24	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18765564
1558097	Zfx	zinc finger protein X-linked	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558097	Zfx	zinc finger protein X-linked	gene	MP:0001606	impaired hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558097	Zfx	zinc finger protein X-linked	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0002086	abnormal extraembryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558097	Zfx	zinc finger protein X-linked	gene	MP:0002088	abnormal embryonic growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0002209	decreased germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0002682	decreased mature ovarian follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558097	Zfx	zinc finger protein X-linked	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558097	Zfx	zinc finger protein X-linked	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558097	Zfx	zinc finger protein X-linked	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558097	Zfx	zinc finger protein X-linked	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558097	Zfx	zinc finger protein X-linked	gene	MP:0008392	decreased primordial germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558097	Zfx	zinc finger protein X-linked	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9187153
1558097	Zfx	zinc finger protein X-linked	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17448993
1558099	Retnlb	resistin like beta	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16815164
1558099	Retnlb	resistin like beta	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16815164
1558099	Retnlb	resistin like beta	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17024245
1558099	Retnlb	resistin like beta	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802073
1558099	Retnlb	resistin like beta	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:17024245
1558099	Retnlb	resistin like beta	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802073
1558099	Retnlb	resistin like beta	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802073
1558099	Retnlb	resistin like beta	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16815164
1558099	Retnlb	resistin like beta	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16815164
1558099	Retnlb	resistin like beta	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17024245
1558099	Retnlb	resistin like beta	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802073
1558099	Retnlb	resistin like beta	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18802073
1558099	Retnlb	resistin like beta	gene	MP:0008597	decreased circulating interleukin-6 level		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0008608	increased circulating interleukin-13 level		IAGP		N	RGD:5509061	20190221	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0009298	increased mesenteric fat pad weight		IAGP		N	RGD:5509061	20240418	MGI			PMID:27397737
1558099	Retnlb	resistin like beta	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17024245
1558099	Retnlb	resistin like beta	gene	MP:0031602	white adipose tissue inflammation		IAGP		N	RGD:5509061	20240418	MGI			PMID:27397737
1558100	Rspo2	R-spondin 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0000520	absent kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0000528	delayed kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0000553	absent radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0000561	adactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0000579	abnormal nail morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0001676	abnormal apical ectodermal ridge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0002256	abnormal laryngeal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0002765	short fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20220804	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0003855	abnormal forelimb zeugopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0004371	bowed femur		IAGP		N	RGD:5509061	20181011	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0004423	abnormal temporal bone squamous part morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0004538	abnormal maxillary shelf morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0004540	small maxilla		IAGP		N	RGD:5509061	20171019	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0004592	small mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0004596	abnormal mandibular angle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0004912	absent mandibular coronoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0005270	abnormal zygomatic bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0005359	growth retardation of incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0005430	absent fibula		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0006020	decreased tympanic ring size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0006279	abnormal limb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0008494	absence of all nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0008494	absence of all nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0009437	arytenoid and cricoid cartilage fusion		IAGP		N	RGD:5509061	20181108	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0009895	decreased palatine bone horizontal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0009898	maxillary shelf hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782276
1558100	Rspo2	R-spondin 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17904116
1558100	Rspo2	R-spondin 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18067586
1558100	Rspo2	R-spondin 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0011262	abnormal pharyngeal arch mesenchyme morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0013933	short Meckel's cartilage		IAGP		N	RGD:5509061	20170810	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0014281	hindlimb oligodactyly		IAGP		N	RGD:5509061	20230810	MGI			PMID:19233133
1558100	Rspo2	R-spondin 2	gene	MP:0014320	abnormal autopod rotation		IAGP		N	RGD:5509061	20240404	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:22610508
1558100	Rspo2	R-spondin 2	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20220721	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0030258	small mandibular condyloid process		IAGP		N	RGD:5509061	20171019	MGI			PMID:21237142
1558100	Rspo2	R-spondin 2	gene	MP:0030302	abnormal maxillary zygomatic process morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:21237142
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0000479	abnormal enterocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139088
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0000512	intestinal ulcer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139088
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15848800
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0001756	abnormal urination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19139088
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0001906	increased dopamine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158234
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158234
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002626	increased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15848800
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0003184	increased angiotensin I-converting enzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0003352	increased circulating renin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0003544	abnormal vascular endothelial cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782872
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0003985	renal fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782872
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0004183	abnormal sympathetic nervous system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0004221	abnormal iridocorneal angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250911	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0004875	increased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005258	ocular hypertension		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005497	optic nerve cupping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005558	decreased creatinine clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005582	increased renin activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16782872
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005610	increased circulating antidiuretic hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005662	increased circulating adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005662	increased circulating adrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005665	increased circulating noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0005665	increased circulating noradrenaline level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202406
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0006317	decreased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008067	retina ganglion cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008214	increased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158234
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008661	decreased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158234
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0009274	buphthalmos		IAGP		N	RGD:5509061	20141003	MGI			PMID:20140222
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0009812	abnormal bradykinin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16767097
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0009922	increased transitional stage T1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0009926	decreased transitional stage T2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22683124
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0011481	anterior iris synechia		IAGP		N	RGD:5509061	20150430	MGI			PMID:20140222
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:14623913
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0014697	abnormal fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:16782872
1558102	Vav3	vav guanine nucleotide exchange factor 3	gene	MP:0031232	increased circulating angiotensin II level		IAGP		N	RGD:5509061	20210204	MGI			PMID:16767097
1558103	Blnk	B cell linker	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20210826	MGI			
1558103	Blnk	B cell linker	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1558103	Blnk	B cell linker	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12436112
1558103	Blnk	B cell linker	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20210826	MGI			
1558103	Blnk	B cell linker	gene	MP:0000694	spleen hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585562
1558103	Blnk	B cell linker	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10583957
1558103	Blnk	B cell linker	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591180
1558103	Blnk	B cell linker	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11449370
1558103	Blnk	B cell linker	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1558103	Blnk	B cell linker	gene	MP:0001805	decreased IgG level		IEA		N	RGD:5509061	20111116	MGI			
1558103	Blnk	B cell linker	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591180
1558103	Blnk	B cell linker	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1558103	Blnk	B cell linker	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22761313
1558103	Blnk	B cell linker	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12436112
1558103	Blnk	B cell linker	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1558103	Blnk	B cell linker	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10583957
1558103	Blnk	B cell linker	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700474
1558103	Blnk	B cell linker	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12119344
1558103	Blnk	B cell linker	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1558103	Blnk	B cell linker	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585562
1558103	Blnk	B cell linker	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591180
1558103	Blnk	B cell linker	gene	MP:0002403	abnormal pre-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618482
1558103	Blnk	B cell linker	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10583957
1558103	Blnk	B cell linker	gene	MP:0002460	decreased immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1558103	Blnk	B cell linker	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0002607	decreased basophil cell number		IEA		N	RGD:5509061	20210826	MGI			
1558103	Blnk	B cell linker	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591180
1558103	Blnk	B cell linker	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12119344
1558103	Blnk	B cell linker	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12436112
1558103	Blnk	B cell linker	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528332
1558103	Blnk	B cell linker	gene	MP:0004953	decreased spleen weight		IEA		N	RGD:5509061	20210826	MGI			
1558103	Blnk	B cell linker	gene	MP:0004978	decreased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20210826	MGI			
1558103	Blnk	B cell linker	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1558103	Blnk	B cell linker	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700474
1558103	Blnk	B cell linker	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12119344
1558103	Blnk	B cell linker	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585562
1558103	Blnk	B cell linker	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15528332
1558103	Blnk	B cell linker	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700474
1558103	Blnk	B cell linker	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12618482
1558103	Blnk	B cell linker	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20111116	MGI			
1558103	Blnk	B cell linker	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20111116	MGI			
1558103	Blnk	B cell linker	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10583957
1558103	Blnk	B cell linker	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10583957
1558103	Blnk	B cell linker	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10583957
1558103	Blnk	B cell linker	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700474
1558103	Blnk	B cell linker	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585562
1558103	Blnk	B cell linker	gene	MP:0008189	increased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12119344
1558103	Blnk	B cell linker	gene	MP:0008190	decreased transitional stage B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700474
1558103	Blnk	B cell linker	gene	MP:0008204	absent B-1b cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:10583957
1558103	Blnk	B cell linker	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700474
1558103	Blnk	B cell linker	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12119344
1558103	Blnk	B cell linker	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133609
1558103	Blnk	B cell linker	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10583957
1558103	Blnk	B cell linker	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591180
1558103	Blnk	B cell linker	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700474
1558103	Blnk	B cell linker	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1558103	Blnk	B cell linker	gene	MP:0008212	absent mature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0008213	absent immature B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700474
1558103	Blnk	B cell linker	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12818163
1558103	Blnk	B cell linker	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1558103	Blnk	B cell linker	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10700474
1558103	Blnk	B cell linker	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585562
1558103	Blnk	B cell linker	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10591180
1558103	Blnk	B cell linker	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15331445
1558103	Blnk	B cell linker	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008781	abnormal B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16481047
1558103	Blnk	B cell linker	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585562
1558103	Blnk	B cell linker	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20190509	MGI			PMID:24888588
1558103	Blnk	B cell linker	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10583957
1558103	Blnk	B cell linker	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16585562
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19243221
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19243221
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19243221
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19243221
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623363
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21734292
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0003635	abnormal synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623363
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20180412	MGI			PMID:25126785
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0009244	abnormal acid-activated cation-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21623363
1558106	Neto1	neuropilin (NRP) and tolloid (TLL)-like 1	gene	MP:0011274	short excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20240418	MGI			PMID:21734292
1558109	Tcf20	transcription factor 20	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20201022	MGI			
1558109	Tcf20	transcription factor 20	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0001409	increased stereotypic behavior		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20201022	MGI			
1558109	Tcf20	transcription factor 20	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1558109	Tcf20	transcription factor 20	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1558109	Tcf20	transcription factor 20	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1558109	Tcf20	transcription factor 20	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1558109	Tcf20	transcription factor 20	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1558109	Tcf20	transcription factor 20	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20181227	MGI			
1558109	Tcf20	transcription factor 20	gene	MP:0010865	prenatal growth retardation		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558109	Tcf20	transcription factor 20	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20210812	MGI			PMID:32510763
1558111	Sh3rf3	SH3 domain containing ring finger 3	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20240523	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20201231	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20201022	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20210128	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0003928	increased heart rate variability		IEA		N	RGD:5509061	20260402	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20260402	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160421	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0010574	dilated aorta		IEA		N	RGD:5509061	20160421	MGI			
1558112	Lsm1	LSM1 homolog, mRNA degradation associated	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558113	Il17rd	interleukin 17 receptor D	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442811
1558113	Il17rd	interleukin 17 receptor D	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15729686
1558113	Il17rd	interleukin 17 receptor D	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20210520	MGI			
1558113	Il17rd	interleukin 17 receptor D	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442811
1558113	Il17rd	interleukin 17 receptor D	gene	MP:0012490	abnormal cochlear VIII nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442811
1558114	Zfp341	zinc finger protein 341	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20181227	MGI			
1558114	Zfp341	zinc finger protein 341	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1558114	Zfp341	zinc finger protein 341	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1558114	Zfp341	zinc finger protein 341	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1558117	Lbx2	ladybird homeobox 2	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1558117	Lbx2	ladybird homeobox 2	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1558117	Lbx2	ladybird homeobox 2	gene	MP:0000961	abnormal dorsal root ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1558117	Lbx2	ladybird homeobox 2	gene	MP:0001081	abnormal cranial ganglia morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1558117	Lbx2	ladybird homeobox 2	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17492753
1558117	Lbx2	ladybird homeobox 2	gene	MP:0010768	mortality/aging		IAGP		N	RGD:5509061	20201029	MGI			PMID:17492753
1558118	Wasf1	WASP family, member 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578964
1558118	Wasf1	WASP family, member 1	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578964
1558118	Wasf1	WASP family, member 1	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578964
1558118	Wasf1	WASP family, member 1	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578964
1558118	Wasf1	WASP family, member 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578964
1558118	Wasf1	WASP family, member 1	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215396
1558118	Wasf1	WASP family, member 1	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215396
1558118	Wasf1	WASP family, member 1	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578964
1558118	Wasf1	WASP family, member 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12578964
1558118	Wasf1	WASP family, member 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215396
1558118	Wasf1	WASP family, member 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215396
1558118	Wasf1	WASP family, member 1	gene	MP:0002888	abnormal NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215396
1558118	Wasf1	WASP family, member 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215396
1558118	Wasf1	WASP family, member 1	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215396
1558118	Wasf1	WASP family, member 1	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215396
1558118	Wasf1	WASP family, member 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17215396
1558118	Wasf1	WASP family, member 1	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0008109	abnormal small intestinal microvillus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0009413	skeletal muscle fiber atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20161222	MGI			PMID:12716942
1558118	Wasf1	WASP family, member 1	gene	MP:0012489	abnormal retrosplenial region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12716942
1558119	Zbtb8os	zinc finger and BTB domain containing 8 opposite strand	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20260402	MGI			
1558119	Zbtb8os	zinc finger and BTB domain containing 8 opposite strand	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20260402	MGI			
1558119	Zbtb8os	zinc finger and BTB domain containing 8 opposite strand	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20241121	MGI			
1558121	Usp10	ubiquitin specific peptidase 10	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230274
1558121	Usp10	ubiquitin specific peptidase 10	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230274
1558121	Usp10	ubiquitin specific peptidase 10	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23230274
1558121	Usp10	ubiquitin specific peptidase 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558122	Sirt2	sirtuin 2	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1558122	Sirt2	sirtuin 2	gene	MP:0000630	mammary gland hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949390
1558122	Sirt2	sirtuin 2	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364049
1558122	Sirt2	sirtuin 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20141003	MGI			
1558122	Sirt2	sirtuin 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511966
1558122	Sirt2	sirtuin 2	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23468428
1558122	Sirt2	sirtuin 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364049
1558122	Sirt2	sirtuin 2	gene	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23468428
1558122	Sirt2	sirtuin 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949390
1558122	Sirt2	sirtuin 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1558122	Sirt2	sirtuin 2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511966
1558122	Sirt2	sirtuin 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23468428
1558122	Sirt2	sirtuin 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23468428
1558122	Sirt2	sirtuin 2	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23468428
1558122	Sirt2	sirtuin 2	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1558122	Sirt2	sirtuin 2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364049
1558122	Sirt2	sirtuin 2	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21949390
1558122	Sirt2	sirtuin 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23364049
1558122	Sirt2	sirtuin 2	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23468428
1558122	Sirt2	sirtuin 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:22511966
1558122	Sirt2	sirtuin 2	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0010301	increased stomach tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0010357	increased prostate gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22014574
1558122	Sirt2	sirtuin 2	gene	MP:0014648	abnormal response to nerve crush injury		IAGP		N	RGD:5509061	20250306	MGI			PMID:21949390
1558125	Coasy	Coenzyme A synthase	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230119	MGI			
1558125	Coasy	Coenzyme A synthase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0001391	abnormal tail movements		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0005356	positive geotaxis		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20230119	MGI			
1558125	Coasy	Coenzyme A synthase	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1558125	Coasy	Coenzyme A synthase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20230601	MGI			
1558125	Coasy	Coenzyme A synthase	gene	MP:0020365	increased brain iron level		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0020879	abnormal calcium level		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558125	Coasy	Coenzyme A synthase	gene	MP:0020883	abnormal magnesium level		IAGP		N	RGD:5509061	20210128	MGI			PMID:33352696
1558126	Zfp711	zinc finger protein 711	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20241121	MGI			
1558126	Zfp711	zinc finger protein 711	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20241121	MGI			
1558126	Zfp711	zinc finger protein 711	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20241121	MGI			
1558128	Evx1	even-skipped homeobox 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958869
1558128	Evx1	even-skipped homeobox 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958869
1558128	Evx1	even-skipped homeobox 1	gene	MP:0012102	absent trophectoderm		IAGP		N	RGD:5509061	20141003	MGI			PMID:7958869
1558128	Evx1	even-skipped homeobox 1	gene	MP:0021102	abnormal ventral interneuron 0 morphology		IAGP		N	RGD:5509061	20220310	MGI			PMID:11239430
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0000904	abnormal superior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0002892	decreased superior colliculus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0006104	abnormal tectum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11071772
1558129	Tal2	T cell acute lymphocytic leukemia 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1558130	Nsun4	NOL1/NOP2/Sun domain family, member 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190509	MGI			PMID:24516400
1558130	Nsun4	NOL1/NOP2/Sun domain family, member 4	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20190509	MGI			PMID:24516400
1558130	Nsun4	NOL1/NOP2/Sun domain family, member 4	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20190509	MGI			PMID:24516400
1558130	Nsun4	NOL1/NOP2/Sun domain family, member 4	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20190509	MGI			PMID:24516400
1558130	Nsun4	NOL1/NOP2/Sun domain family, member 4	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20190509	MGI			PMID:24516400
1558130	Nsun4	NOL1/NOP2/Sun domain family, member 4	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20190509	MGI			PMID:24516400
1558130	Nsun4	NOL1/NOP2/Sun domain family, member 4	gene	MP:0030937	increased mitochondrial DNA content		IAGP		N	RGD:5509061	20240718	MGI			PMID:24516400
1558130	Nsun4	NOL1/NOP2/Sun domain family, member 4	gene	MP:0031748	impaired mitochondrial translation		IAGP		N	RGD:5509061	20260716	MGI			PMID:24516400
1558131	Coq9	coenzyme Q9	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0005114	premature hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0008143	abnormal dendrite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0014775	decreased skeletal muscle enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0014777	decreased heart enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0014779	decreased brain enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0014781	decreased kidney enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:23255162
1558131	Coq9	coenzyme Q9	gene	MP:0014783	decreased liver enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:23255162
1558132	Slfn8	schlafen 8	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20210429	MGI			PMID:29528433
1558132	Slfn8	schlafen 8	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20210429	MGI			PMID:29528433
1558132	Slfn8	schlafen 8	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20210429	MGI			PMID:29528433
1558132	Slfn8	schlafen 8	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20210429	MGI			PMID:29528433
1558132	Slfn8	schlafen 8	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20210429	MGI			PMID:29528433
1558133	Iqcf1	IQ motif containing F1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20160324	MGI			PMID:25380116
1558133	Iqcf1	IQ motif containing F1	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20160324	MGI			PMID:25380116
1558133	Iqcf1	IQ motif containing F1	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20160324	MGI			PMID:25380116
1558133	Iqcf1	IQ motif containing F1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210826	MGI			
1558134	Lrsam1	leucine rich repeat and sterile alpha motif containing 1	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23519028
1558134	Lrsam1	leucine rich repeat and sterile alpha motif containing 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:23519028
1558134	Lrsam1	leucine rich repeat and sterile alpha motif containing 1	gene	MP:0004263	abnormal limb posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:23519028
1558134	Lrsam1	leucine rich repeat and sterile alpha motif containing 1	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23519028
1558134	Lrsam1	leucine rich repeat and sterile alpha motif containing 1	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23519028
1558134	Lrsam1	leucine rich repeat and sterile alpha motif containing 1	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20231207	MGI			
1558134	Lrsam1	leucine rich repeat and sterile alpha motif containing 1	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23519028
1558134	Lrsam1	leucine rich repeat and sterile alpha motif containing 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230601	MGI			
1558135	Rnf128	ring finger protein 128	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20201022	MGI			
1558135	Rnf128	ring finger protein 128	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:28581443
1558135	Rnf128	ring finger protein 128	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0005000	abnormal immune tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805371
1558135	Rnf128	ring finger protein 128	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805371
1558135	Rnf128	ring finger protein 128	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805371
1558135	Rnf128	ring finger protein 128	gene	MP:0006082	CNS inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805371
1558135	Rnf128	ring finger protein 128	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008568	abnormal interleukin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008599	increased circulating interleukin-2 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805371
1558135	Rnf128	ring finger protein 128	gene	MP:0008673	decreased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008703	decreased interleukin-5 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0008749	abnormal peripheral T cell anergy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805371
1558135	Rnf128	ring finger protein 128	gene	MP:0009057	increased interleukin-21 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0009336	increased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20493730
1558135	Rnf128	ring finger protein 128	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20201022	MGI			
1558135	Rnf128	ring finger protein 128	gene	MP:0012564	decreased tumor incidence following infection		IAGP		N	RGD:5509061	20241114	MGI			PMID:36103821
1558135	Rnf128	ring finger protein 128	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20211021	MGI			
1558136	Elp4	elongator acetyltransferase complex subunit 4	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20241121	MGI			
1558136	Elp4	elongator acetyltransferase complex subunit 4	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20240523	MGI			
1558136	Elp4	elongator acetyltransferase complex subunit 4	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1558136	Elp4	elongator acetyltransferase complex subunit 4	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1558136	Elp4	elongator acetyltransferase complex subunit 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1558136	Elp4	elongator acetyltransferase complex subunit 4	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20250508	MGI			
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0004025	polyploidy		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0004045	abnormal cell cycle checkpoint function		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0008057	abnormal DNA replication		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0014178	increased brain apoptosis		IAGP		N	RGD:5509061	20190328	MGI			PMID:30232008
1558137	Ercc6l	excision repair cross-complementing rodent repair deficiency complementation group 6 like	gene	MP:0031678	increased micronucleus incidence		IAGP		N	RGD:5509061	20250814	MGI			PMID:30232008
1558138	Lrrc63	leucine rich repeat containing 63	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20241121	MGI			
1558138	Lrrc63	leucine rich repeat containing 63	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20250508	MGI			
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:16056226
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672341
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672341
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16056226
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16056226
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16672341
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0008395	abnormal osteoblast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16056226
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16056226
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0013754	abnormal ocular surface morphology		IAGP		N	RGD:5509061	20150416	MGI			PMID:16672341
1558139	Dkk2	dickkopf WNT signaling pathway inhibitor 2	gene	MP:0020857	cornea epithelium hyperplasia		IAGP		N	RGD:5509061	20181101	MGI			PMID:16672341
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0000794	abnormal parietal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0000798	abnormal frontal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20230601	MGI			
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0003054	spina bifida		IEA		N	RGD:5509061	20230601	MGI			
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20181004	MGI			
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0005623	abnormal meninges morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0005630	increased lung weight		IEA		N	RGD:5509061	20230601	MGI			
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0009026	abnormal brain pia mater morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16407979
1558141	Apbb2	amyloid beta precursor protein binding family B member 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0000383	abnormal hair follicle orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357712
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0000420	ruffled hair		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357712
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0000919	cranioschisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357712
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220519	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001148	enlarged testis		IEA		N	RGD:5509061	20220519	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20220519	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001341	absent eyelids		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001394	circling		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932191
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001411	spinning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20241121	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001850	increased susceptibility to otitis media		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001891	hydrocephaly		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001921	reduced fertility		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20220811	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20220811	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0001967	deafness		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0002080	prenatal lethality		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0002111	abnormal tail morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0002152	abnormal brain morphology		IEA		N	RGD:5509061	20220519	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0002730	head shaking		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:20704721
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003054	spina bifida		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003205	testicular atrophy		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003257	abnormal abdominal wall morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003308	abnormal cochlear sensory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003492	abnormal involuntary movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:10932191
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357712
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0004300	abnormal organ of Corti supporting cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0004391	abnormal respiratory conducting tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0004491	abnormal orientation of outer hair cell stereociliary bundles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0005238	increased brain size		IEA		N	RGD:5509061	20220519	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0005307	head tossing		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0005657	abnormal neural plate morphology		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0006026	dilated terminal bronchiole tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0006325	impaired hearing		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0006382	abnormal lung epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0009457	whorled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357712
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0009651	abnormal eyelid development		IAGP		N	RGD:5509061	20151001	MGI			PMID:25128525
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0010975	abnormal lung lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0010976	small lung lobe		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0011032	impaired branching involved in terminal bronchiole morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12842012
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19357712
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0011143	thick lung-associated mesenchyme		IAGP		N	RGD:5509061	20141003	MGI			PMID:20223754
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IEA		N	RGD:5509061	20160324	MGI			
1558142	Celsr1	cadherin, EGF LAG seven-pass G-type receptor 1	gene	MP:0030961	abnormal outer hair cell kinocilium location or orientation		IAGP		N	RGD:5509061	20190725	MGI			PMID:12842012
1558143	Rbmx	RNA binding motif protein, X chromosome	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1558143	Rbmx	RNA binding motif protein, X chromosome	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1558143	Rbmx	RNA binding motif protein, X chromosome	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1558143	Rbmx	RNA binding motif protein, X chromosome	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1558143	Rbmx	RNA binding motif protein, X chromosome	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20210128	MGI			
1558143	Rbmx	RNA binding motif protein, X chromosome	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556408
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20525685
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20525685
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363774
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20525685
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556408
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20151119	MGI			PMID:23448972
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20525685
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20151119	MGI			PMID:23448972
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20695981
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0002551	abnormal blood coagulation		IAGP		N	RGD:5509061	20151119	MGI			PMID:23448972
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0002843	decreased systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0003288	intestinal edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363774
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0003288	intestinal edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:22556408
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0005324	ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20695981
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20151119	MGI			PMID:23448972
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0006054	spinal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20363774
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0006298	abnormal platelet activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20525685
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0008247	abnormal mononuclear cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20525685
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0010022	brain vascular congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0010197	abnormal lymphatic vessel endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0010198	decreased lymphatic vessel endothelial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0010368	abnormal lymphatic system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20525685
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0010819	primary atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20525685
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20695981
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20695981
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20525685
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20562862
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011514	skin hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0011898	abnormal platelet cell number		IAGP		N	RGD:5509061	20151119	MGI			PMID:23448972
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:22186994
1558144	Clec1b	C-type lectin domain family 1, member b	gene	MP:0031051	lymph node hemorrhage		IAGP		N	RGD:5509061	20201015	MGI			PMID:23995678
1558145	Rab33a	RAB33A, member RAS oncogene family	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20221215	MGI			
1558146	Tceal1	transcription elongation factor A (SII)-like 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20190502	MGI			
1558146	Tceal1	transcription elongation factor A (SII)-like 1	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20190502	MGI			
1558146	Tceal1	transcription elongation factor A (SII)-like 1	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20210128	MGI			
1558146	Tceal1	transcription elongation factor A (SII)-like 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1558147	H2-Eb1	histocompatibility 2, class II antigen E beta	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20231207	MGI			
1558148	Fmr1nb	Fmr1 neighbor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180830	MGI			PMID:27357688
1558149	Zfp61	zinc finger protein 61	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1558149	Zfp61	zinc finger protein 61	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20210520	MGI			
1558149	Zfp61	zinc finger protein 61	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20181227	MGI			
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20111116	MGI			
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20250508	MGI			
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0001353	increased aggression towards mice		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0002084	abnormal developmental patterning		IEA		N	RGD:5509061	20111116	MGI			
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20250508	MGI			
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0002781	increased circulating testosterone level		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0010698	abnormal impulsive behavior control		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20221222	MGI			
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20250508	MGI			
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0020337	abnormal pyramidal neuron dendrite morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558152	Kdm5c	lysine demethylase 5C	gene	MP:0020512	abnormal dendritic mushroom spine morphology		IAGP		N	RGD:5509061	20180712	MGI			PMID:26804915
1558154	Appl2	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1558154	Appl2	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2	gene	MP:0002608	increased hematocrit		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1558154	Appl2	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20160505	MGI			PMID:24879834
1558154	Appl2	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20160505	MGI			PMID:24879834
1558154	Appl2	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1558154	Appl2	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1558154	Appl2	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20260326	MGI			PMID:39201474
1558154	Appl2	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2	gene	MP:0011708	decreased fibroblast cell migration		IAGP		N	RGD:5509061	20160519	MGI			PMID:26445298
1558154	Appl2	adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:24879834
1558155	H2ax	H2A.X variant histone	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934988
1558155	H2ax	H2A.X variant histone	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19377486
1558155	H2ax	H2A.X variant histone	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934988
1558155	H2ax	H2A.X variant histone	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934988
1558155	H2ax	H2A.X variant histone	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934988
1558155	H2ax	H2A.X variant histone	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934988
1558155	H2ax	H2A.X variant histone	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11740565
1558155	H2ax	H2A.X variant histone	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0002021	increased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914701
1558155	H2ax	H2A.X variant histone	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914701
1558155	H2ax	H2A.X variant histone	gene	MP:0002627	increased teratoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19377486
1558155	H2ax	H2A.X variant histone	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19377486
1558155	H2ax	H2A.X variant histone	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599436
1558155	H2ax	H2A.X variant histone	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810694
1558155	H2ax	H2A.X variant histone	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23254285
1558155	H2ax	H2A.X variant histone	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934988
1558155	H2ax	H2A.X variant histone	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934988
1558155	H2ax	H2A.X variant histone	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11934988
1558155	H2ax	H2A.X variant histone	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19377486
1558155	H2ax	H2A.X variant histone	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599436
1558155	H2ax	H2A.X variant histone	gene	MP:0009314	increased colon adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0010144	abnormal tumor vascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19377486
1558155	H2ax	H2A.X variant histone	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18599436
1558155	H2ax	H2A.X variant histone	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914700
1558155	H2ax	H2A.X variant histone	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12914701
1558155	H2ax	H2A.X variant histone	gene	MP:0012556	increased cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:18599436
1558155	H2ax	H2A.X variant histone	gene	MP:0020316	decreased vascular endothelial cell proliferation		IAGP		N	RGD:5509061	20160616	MGI			PMID:23254285
1558155	H2ax	H2A.X variant histone	gene	MP:0020321	increased vascular endothelial cell apoptosis		IAGP		N	RGD:5509061	20160616	MGI			PMID:19377486
1558156	Emcn	endomucin	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1558156	Emcn	endomucin	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20181227	MGI			
1558156	Emcn	endomucin	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1558156	Emcn	endomucin	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558156	Emcn	endomucin	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20181227	MGI			
1558156	Emcn	endomucin	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1558156	Emcn	endomucin	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20200402	MGI			
1558156	Emcn	endomucin	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558156	Emcn	endomucin	gene	MP:0008059	abnormal podocyte foot process morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558156	Emcn	endomucin	gene	MP:0008139	fused podocyte foot processes		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558156	Emcn	endomucin	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558156	Emcn	endomucin	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1558156	Emcn	endomucin	gene	MP:0011409	increased renal glomerulus basement membrane thickness		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558156	Emcn	endomucin	gene	MP:0011454	abnormal glomerular endothelium fenestra morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558156	Emcn	endomucin	gene	MP:0011499	abnormal glomerular capsule space morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558156	Emcn	endomucin	gene	MP:0011855	abnormal glomerular filtration barrier morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558156	Emcn	endomucin	gene	MP:0011856	abnormal glomerular filtration barrier function		IAGP		N	RGD:5509061	20260129	MGI			PMID:39584795
1558157	Atxn7	ataxin 7	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0000243	myoclonus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0000864	abnormal cerebellum vermis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0001005	abnormal retina rod cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16494529
1558157	Atxn7	ataxin 7	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16494529
1558157	Atxn7	ataxin 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0002922	decreased post-tetanic potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20241121	MGI			
1558157	Atxn7	ataxin 7	gene	MP:0008450	retina photoreceptor degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0008511	thin retina inner nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0008513	thin retina inner plexiform layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0008580	photoreceptor inner segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0008587	short photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1558157	Atxn7	ataxin 7	gene	MP:0010387	abnormal Bergmann glial cell morphology		IAGP		N	RGD:5509061	20180830	MGI			PMID:16936724
1558157	Atxn7	ataxin 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22002997
1558157	Atxn7	ataxin 7	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:12575948
1558157	Atxn7	ataxin 7	gene	MP:0014327	decreased Purkinje cell size		IAGP		N	RGD:5509061	20240118	MGI			PMID:22002997
1558159	Apip	APAF1 interacting protein	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20201022	MGI			
1558161	Dnmbp	dynamin binding protein	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1558161	Dnmbp	dynamin binding protein	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20201022	MGI			
1558161	Dnmbp	dynamin binding protein	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20201022	MGI			
1558161	Dnmbp	dynamin binding protein	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1558161	Dnmbp	dynamin binding protein	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20210826	MGI			
1558161	Dnmbp	dynamin binding protein	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1558161	Dnmbp	dynamin binding protein	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20210826	MGI			
1558161	Dnmbp	dynamin binding protein	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1558161	Dnmbp	dynamin binding protein	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20190502	MGI			
1558162	Plxna3	plexin A3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11683995
1558162	Plxna3	plexin A3	gene	MP:0000815	abnormal Ammon gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11683995
1558162	Plxna3	plexin A3	gene	MP:0000968	abnormal sensory neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721238
1558162	Plxna3	plexin A3	gene	MP:0001063	abnormal trochlear nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721238
1558162	Plxna3	plexin A3	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11683995
1558162	Plxna3	plexin A3	gene	MP:0001065	abnormal trigeminal nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15721238
1558162	Plxna3	plexin A3	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11683995
1558162	Plxna3	plexin A3	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1558162	Plxna3	plexin A3	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1558162	Plxna3	plexin A3	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1558162	Plxna3	plexin A3	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1558162	Plxna3	plexin A3	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1558162	Plxna3	plexin A3	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1558162	Plxna3	plexin A3	gene	MP:0008415	abnormal neurite morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21835343
1558162	Plxna3	plexin A3	gene	MP:0008960	abnormal axon pruning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12732138
1558162	Plxna3	plexin A3	gene	MP:0014745	abnormal hippocampal mossy fiber infrapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:11683995
1558162	Plxna3	plexin A3	gene	MP:0014745	abnormal hippocampal mossy fiber infrapyramidal bundle morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:12732138
1558162	Plxna3	plexin A3	gene	MP:0014748	abnormal sensory neuron axon guidance		IAGP		N	RGD:5509061	20250911	MGI			PMID:15721238
1558163	Hoxb6	homeobox B6	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1558163	Hoxb6	homeobox B6	gene	MP:0000150	abnormal rib morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1558163	Hoxb6	homeobox B6	gene	MP:0000152	absent proximal rib		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1558163	Hoxb6	homeobox B6	gene	MP:0000153	rib bifurcation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1558163	Hoxb6	homeobox B6	gene	MP:0000154	rib fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996827
1558163	Hoxb6	homeobox B6	gene	MP:0002752	abnormal somatic nervous system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1558163	Hoxb6	homeobox B6	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996827
1558163	Hoxb6	homeobox B6	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1558163	Hoxb6	homeobox B6	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10996827
1558163	Hoxb6	homeobox B6	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1558163	Hoxb6	homeobox B6	gene	MP:0004321	short sternum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0004322	abnormal sternebra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0004615	cervical vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1558163	Hoxb6	homeobox B6	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7828847
1558163	Hoxb6	homeobox B6	gene	MP:0004625	abnormal rib joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0004680	small xiphoid process		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0010103	small thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17626057
1558163	Hoxb6	homeobox B6	gene	MP:0015016	enhanced fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:10996827
1558165	Cep41	centrosomal protein 41	gene	MP:0000288	abnormal pericardium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246503
1558165	Cep41	centrosomal protein 41	gene	MP:0000841	abnormal hindbrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246503
1558165	Cep41	centrosomal protein 41	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246503
1558165	Cep41	centrosomal protein 41	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246503
1558165	Cep41	centrosomal protein 41	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246503
1558165	Cep41	centrosomal protein 41	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1558165	Cep41	centrosomal protein 41	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22246503
1558166	Mindy1	MINDY lysine 48 deubiquitinase 1	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1558166	Mindy1	MINDY lysine 48 deubiquitinase 1	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1558166	Mindy1	MINDY lysine 48 deubiquitinase 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20160804	MGI			
1558166	Mindy1	MINDY lysine 48 deubiquitinase 1	gene	MP:0003313	abnormal locomotor activation		IEA		N	RGD:5509061	20141003	MGI			
1558166	Mindy1	MINDY lysine 48 deubiquitinase 1	gene	MP:0003442	decreased circulating glycerol level		IEA		N	RGD:5509061	20160804	MGI			
1558166	Mindy1	MINDY lysine 48 deubiquitinase 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20141003	MGI			
1558167	Prmt2	protein arginine N-methyltransferase 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616919
1558167	Prmt2	protein arginine N-methyltransferase 2	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:16616919
1558167	Prmt2	protein arginine N-methyltransferase 2	gene	MP:0010101	increased sacral vertebrae number		IEA		N	RGD:5509061	20160804	MGI			
1558168	Gins1	GINS complex subunit 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287864
1558168	Gins1	GINS complex subunit 1	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287864
1558168	Gins1	GINS complex subunit 1	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287864
1558168	Gins1	GINS complex subunit 1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287864
1558168	Gins1	GINS complex subunit 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287864
1558168	Gins1	GINS complex subunit 1	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16287864
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0000610	cholestasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0004939	abnormal B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0005517	impaired liver regeneration		IAGP		N	RGD:5509061	20210415	MGI			PMID:32518166
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0005637	abnormal iron homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0008743	decreased liver iron level		IAGP		N	RGD:5509061	20210415	MGI			PMID:32518166
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0008956	decreased cellular hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20210415	MGI			PMID:32518166
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0011178	increased erythroblast number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0014989	impaired erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:21310927
1558169	Slc25a37	solute carrier family 25, member 37	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:21310927
1558172	Tspan18	tetraspanin 18	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1558172	Tspan18	tetraspanin 18	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20220519	MGI			
1558172	Tspan18	tetraspanin 18	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20201022	MGI			
1558172	Tspan18	tetraspanin 18	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210520	MGI			
1558172	Tspan18	tetraspanin 18	gene	MP:0009676	abnormal hemostasis		IAGP		N	RGD:5509061	20210617	MGI			PMID:30573509
1558172	Tspan18	tetraspanin 18	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1558172	Tspan18	tetraspanin 18	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20210617	MGI			PMID:30573509
1558172	Tspan18	tetraspanin 18	gene	MP:0031164	decreased circulating von Willebrand factor level		IAGP		N	RGD:5509061	20210617	MGI			PMID:30573509
1558177	Mfsd6	major facilitator superfamily domain containing 6	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20250626	MGI			PMID:23836286
1558177	Mfsd6	major facilitator superfamily domain containing 6	gene	MP:0004751	increased length of allograft survival		IAGP		N	RGD:5509061	20250626	MGI			PMID:23836286
1558179	Dusp9	dual specificity phosphatase 9	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16135819
1558179	Dusp9	dual specificity phosphatase 9	gene	MP:0004255	abnormal spongiotrophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16135819
1558179	Dusp9	dual specificity phosphatase 9	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16135819
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0000857	abnormal cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0000885	ectopic Purkinje cell		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20240523	MGI			
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20141003	MGI			PMID:16221497
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:16221497
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0002762	ectopic cerebellar granule cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20181227	MGI			
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0008914	enlarged cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0009268	absent cerebellum fissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0009964	abnormal cerebellum lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0009977	abnormal cerebellar granule cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210520	MGI			
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0010387	abnormal Bergmann glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23100420
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16221497
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558180	Ric8a	RIC8 guanine nucleotide exchange factor A	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1558182	Cenpa	centromere protein A	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0002884	abnormal pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0003702	abnormal chromosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655499
1558182	Cenpa	centromere protein A	gene	MP:0004965	inner cell mass degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655499
1558182	Cenpa	centromere protein A	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655499
1558182	Cenpa	centromere protein A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558182	Cenpa	centromere protein A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10655499
1558182	Cenpa	centromere protein A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12906131
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0000021	prominent ears		IAGP		N	RGD:5509061	20171019	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220922	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0000749	muscle degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0001330	abnormal optic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20141003	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20160804	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002001	blindness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002327	abnormal respiratory function		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20141003	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002697	abnormal eye size		IEA		N	RGD:5509061	20141003	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002750	exophthalmos		IAGP		N	RGD:5509061	20171019	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20160804	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20141003	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0003866	abnormal defecation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0004087	abnormal muscle fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0004089	dilated sarcoplasmic reticulum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0004734	small thoracic cavity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20141003	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20141003	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0005586	decreased tidal volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20141003	MGI			
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0008852	retina neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0009346	decreased trabecular bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0009409	abnormal skeletal muscle fiber type ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0011633	abnormal mitochondrial shape		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0011942	decreased fluid intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0020010	decreased bone mineral density of femur		IAGP		N	RGD:5509061	20220915	MGI			PMID:19451219
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20190711	MGI			PMID:22343142
1558185	Cisd2	CDGSH iron sulfur domain 2	gene	MP:0031253	lordokyphosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:19451219
1558188	Tmem43	transmembrane protein 43	gene	MP:0001363	increased anxiety-related response		IEA		N	RGD:5509061	20141003	MGI			
1558188	Tmem43	transmembrane protein 43	gene	MP:0004300	abnormal organ of Corti supporting cell morphology		IAGP		N	RGD:5509061	20220331	MGI			PMID:34050020
1558188	Tmem43	transmembrane protein 43	gene	MP:0004396	decreased cochlear inner hair cell number		IAGP		N	RGD:5509061	20220331	MGI			PMID:34050020
1558188	Tmem43	transmembrane protein 43	gene	MP:0004739	conductive hearing loss		IAGP		N	RGD:5509061	20220331	MGI			PMID:34050020
1558188	Tmem43	transmembrane protein 43	gene	MP:0011966	abnormal auditory brainstem response waveform shape		IAGP		N	RGD:5509061	20220331	MGI			PMID:34050020
1558188	Tmem43	transmembrane protein 43	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20220331	MGI			PMID:34050020
1558188	Tmem43	transmembrane protein 43	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:34050020
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000813	abnormal hippocampus layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000853	absent cerebellar foliation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000854	abnormal cerebellum development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000872	abnormal cerebellum external granule cell layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0001491	unresponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0002883	chromatolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0009718	absent Purkinje cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558190	Cdk5r2	cyclin dependent kinase 5, regulatory subunit 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11517264
1558191	Hunk	hormonally upregulated Neu-associated kinase	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19717424
1558191	Hunk	hormonally upregulated Neu-associated kinase	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20201022	MGI			
1558191	Hunk	hormonally upregulated Neu-associated kinase	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19717424
1558191	Hunk	hormonally upregulated Neu-associated kinase	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1558191	Hunk	hormonally upregulated Neu-associated kinase	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1558192	Itsn2	intersectin 2	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20150430	MGI			
1558192	Itsn2	intersectin 2	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23447614
1558192	Itsn2	intersectin 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23447614
1558192	Itsn2	intersectin 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1558192	Itsn2	intersectin 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:23447614
1558192	Itsn2	intersectin 2	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1558192	Itsn2	intersectin 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23447614
1558192	Itsn2	intersectin 2	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20180802	MGI			PMID:29773874
1558192	Itsn2	intersectin 2	gene	MP:0008026	abnormal brain white matter morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23447614
1558192	Itsn2	intersectin 2	gene	MP:0008140	podocyte foot process effacement		IAGP		N	RGD:5509061	20180802	MGI			PMID:29773874
1558192	Itsn2	intersectin 2	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23447614
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0012220	abnormal ether lipid level		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558194	Far1	fatty acyl CoA reductase 1	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20230921	MGI			PMID:37039784
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937813
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937813
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240314	MGI			PMID:34901307
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:14555645
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937813
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001436	abnormal suckling behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:14555645
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20240314	MGI			PMID:34901307
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:14555645
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937813
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20240314	MGI			PMID:34901307
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937813
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002703	abnormal renal tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003030	acidemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937813
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003031	acidosis		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003620	oliguria		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:14555645
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0004756	abnormal proximal convoluted tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005217	abnormal pancreatic beta cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20160804	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005280	abnormal fatty acids level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005309	increased circulating ammonia level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0005619	increased urine potassium level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0008986	abnormal liver parenchyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14555645
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:14555645
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937813
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0010028	aciduria		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937813
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0010955	abnormal respiratory electron transport chain		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0010958	abnormal tricarboxylic acid cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17937813
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20240314	MGI			PMID:34901307
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14555645
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011405	tubulointerstitial nephritis		IAGP		N	RGD:5509061	20180906	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011435	increased urine magnesium level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0012230	abnormal sphingolipid level		IAGP		N	RGD:5509061	20180531	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0030612	organic aciduria		IAGP		N	RGD:5509061	20180906	MGI			PMID:19088183
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0030614	methylmalonic aciduria		IAGP		N	RGD:5509061	20180906	MGI			PMID:14555645
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0030614	methylmalonic aciduria		IAGP		N	RGD:5509061	20180906	MGI			PMID:23024777
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0030614	methylmalonic aciduria		IAGP		N	RGD:5509061	20180906	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0030630	increased circulating methylmalonic acid level		IAGP		N	RGD:5509061	20220120	MGI			PMID:23898205
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0030630	increased circulating methylmalonic acid level		IAGP		N	RGD:5509061	20240314	MGI			PMID:34901307
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0030655	increased circulating glycine level		IAGP		N	RGD:5509061	20180913	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0031339	increased lipocalin 2 level		IAGP		N	RGD:5509061	20220120	MGI			PMID:27519416
1558195	Mmut	methylmalonyl-Coenzyme A mutase	gene	MP:0031342	increased circulating lipocalin 2 level		IAGP		N	RGD:5509061	20220120	MGI			PMID:23898205
1558196	Slc29a4	solute carrier family 29 (nucleoside transporters), member 4	gene	MP:0000552	abnormal radius morphology		IEA		N	RGD:5509061	20200514	MGI			
1558196	Slc29a4	solute carrier family 29 (nucleoside transporters), member 4	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23255610
1558196	Slc29a4	solute carrier family 29 (nucleoside transporters), member 4	gene	MP:0005108	abnormal ulna morphology		IEA		N	RGD:5509061	20200514	MGI			
1558196	Slc29a4	solute carrier family 29 (nucleoside transporters), member 4	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20250508	MGI			
1558197	Cabp2	calcium binding protein 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1558197	Cabp2	calcium binding protein 2	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1558197	Cabp2	calcium binding protein 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1558197	Cabp2	calcium binding protein 2	gene	MP:0004433	abnormal cochlear inner hair cell physiology		IAGP		N	RGD:5509061	20180524	MGI			PMID:28183797
1558197	Cabp2	calcium binding protein 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1558197	Cabp2	calcium binding protein 2	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20180531	MGI			PMID:27822497
1558197	Cabp2	calcium binding protein 2	gene	MP:0006335	abnormal hearing electrophysiology		IAGP		N	RGD:5509061	20180524	MGI			PMID:28183797
1558197	Cabp2	calcium binding protein 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20180524	MGI			PMID:28183797
1558197	Cabp2	calcium binding protein 2	gene	MP:0031671	decreased auditory brainstem response wave amplitude		IAGP		N	RGD:5509061	20250814	MGI			PMID:28183797
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000017	big ears		IEA		N	RGD:5509061	20111116	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1166079
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000379	decreased hair follicle number		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:1166079
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000416	sparse hair		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000417	short hair		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000418	focal hair loss		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:133823
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:133823
1558198	Edaradd	EDAR associated via death domain	gene	MP:0000921	demyelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:1166079
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1166079
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001265	decreased body size		IEA		N	RGD:5509061	20111116	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001340	abnormal eyelid morphology		IEA		N	RGD:5509061	20111116	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20111116	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:133823
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0001950	abnormal respiratory sounds		IEA		N	RGD:5509061	20111116	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20141003	MGI			PMID:320066
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002074	abnormal hair texture		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1166079
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:1166079
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:133823
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002095	abnormal skin pigmentation		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20111116	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002277	abnormal respiratory mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15973734
1558198	Edaradd	EDAR associated via death domain	gene	MP:0002576	abnormal enamel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1558198	Edaradd	EDAR associated via death domain	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:133823
1558198	Edaradd	EDAR associated via death domain	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:133823
1558198	Edaradd	EDAR associated via death domain	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:478295
1558198	Edaradd	EDAR associated via death domain	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1558198	Edaradd	EDAR associated via death domain	gene	MP:0006236	absent Meibomian glands		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1558198	Edaradd	EDAR associated via death domain	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0006366	absent zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1558198	Edaradd	EDAR associated via death domain	gene	MP:0006366	absent zigzag hairs		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1558198	Edaradd	EDAR associated via death domain	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:478295
1558198	Edaradd	EDAR associated via death domain	gene	MP:0006402	small molars		IAGP		N	RGD:5509061	20141003	MGI			PMID:5893447
1558198	Edaradd	EDAR associated via death domain	gene	MP:0009267	abnormal cerebellum fissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0009825	cornea ulcer		IEA		N	RGD:5509061	20160310	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0009956	abnormal cerebellar layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:896803
1558198	Edaradd	EDAR associated via death domain	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0012078	abnormal tail ring morphology		IEA		N	RGD:5509061	20170309	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0013176	abnormal tail position or orientation		IEA		N	RGD:5509061	20141003	MGI			
1558198	Edaradd	EDAR associated via death domain	gene	MP:0013897	decreased eyelid cilium number		IAGP		N	RGD:5509061	20200123	MGI			PMID:24539712
1558198	Edaradd	EDAR associated via death domain	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20171221	MGI			PMID:5893447
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20231207	MGI			
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0001545	abnormal hematopoietic system physiology		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0001658	increased mortality induced by gamma-irradiation		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0005013	increased lymphocyte cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0011182	decreased hematopoietic cell number		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0011902	increased hematopoietic stem cell proliferation		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0013694	abnormal granulocyte monocyte progenitor cell morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558200	Ang	angiogenin, ribonuclease, RNase A family, 5	gene	MP:0013702	abnormal megakaryocyte-erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20190103	MGI			PMID:27518564
1558202	Tmem114	transmembrane protein 114	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20201022	MGI			PMID:32588039
1558203	Zfp827	zinc finger protein 827	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20240523	MGI			
1558203	Zfp827	zinc finger protein 827	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1558203	Zfp827	zinc finger protein 827	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20201231	MGI			
1558203	Zfp827	zinc finger protein 827	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558207	Cdk17	cyclin dependent kinase 17	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20240523	MGI			
1558207	Cdk17	cyclin dependent kinase 17	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1558207	Cdk17	cyclin dependent kinase 17	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1558207	Cdk17	cyclin dependent kinase 17	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1558207	Cdk17	cyclin dependent kinase 17	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558208	Cd209d	CD209d antigen	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770268
1558208	Cd209d	CD209d antigen	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1558208	Cd209d	CD209d antigen	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1558208	Cd209d	CD209d antigen	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19770268
1558208	Cd209d	CD209d antigen	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20150226	MGI			PMID:23118208
1558212	Ahctf1	AT hook containing transcription factor 1	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20210520	MGI			
1558212	Ahctf1	AT hook containing transcription factor 1	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15507119
1558212	Ahctf1	AT hook containing transcription factor 1	gene	MP:0010380	abnormal inner cell mass apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15507119
1558212	Ahctf1	AT hook containing transcription factor 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15507119
1558212	Ahctf1	AT hook containing transcription factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558212	Ahctf1	AT hook containing transcription factor 1	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15507119
1558214	Rspo3	R-spondin 3	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20150716	MGI			PMID:25053429
1558214	Rspo3	R-spondin 3	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20150129	MGI			PMID:18842812
1558214	Rspo3	R-spondin 3	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20150716	MGI			PMID:25053429
1558214	Rspo3	R-spondin 3	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0000561	adactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16963017
1558214	Rspo3	R-spondin 3	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:18842812
1558214	Rspo3	R-spondin 3	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16963017
1558214	Rspo3	R-spondin 3	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20150129	MGI			PMID:18842812
1558214	Rspo3	R-spondin 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16963017
1558214	Rspo3	R-spondin 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20150129	MGI			PMID:18842812
1558214	Rspo3	R-spondin 3	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20150716	MGI			PMID:25053429
1558214	Rspo3	R-spondin 3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20150129	MGI			PMID:18842812
1558214	Rspo3	R-spondin 3	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20150716	MGI			PMID:25053429
1558214	Rspo3	R-spondin 3	gene	MP:0002728	absent tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20150129	MGI			PMID:18842812
1558214	Rspo3	R-spondin 3	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20150716	MGI			PMID:25053429
1558214	Rspo3	R-spondin 3	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20150716	MGI			PMID:25053429
1558214	Rspo3	R-spondin 3	gene	MP:0004371	bowed femur		IAGP		N	RGD:5509061	20181011	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20150716	MGI			PMID:25053429
1558214	Rspo3	R-spondin 3	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16963017
1558214	Rspo3	R-spondin 3	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16963017
1558214	Rspo3	R-spondin 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22610508
1558214	Rspo3	R-spondin 3	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20150716	MGI			PMID:25053429
1558214	Rspo3	R-spondin 3	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20150716	MGI			PMID:25053429
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470613
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0002217	small lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1558216	Dach2	dachshund family transcription factor 2	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20230601	MGI			
1558220	Siglece	sialic acid binding Ig-like lectin E	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180913	MGI			PMID:28100677
1558220	Siglece	sialic acid binding Ig-like lectin E	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23315163
1558220	Siglece	sialic acid binding Ig-like lectin E	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23315163
1558220	Siglece	sialic acid binding Ig-like lectin E	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20180913	MGI			PMID:28100677
1558220	Siglece	sialic acid binding Ig-like lectin E	gene	MP:0008617	increased circulating interleukin-12 level		IAGP		N	RGD:5509061	20180913	MGI			PMID:28100677
1558220	Siglece	sialic acid binding Ig-like lectin E	gene	MP:0014902	increased circulating CCL2 level		IAGP		N	RGD:5509061	20260219	MGI			PMID:28100677
1558222	Kcnk5	potassium channel, subfamily K, member 5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15141089
1558222	Kcnk5	potassium channel, subfamily K, member 5	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133877
1558222	Kcnk5	potassium channel, subfamily K, member 5	gene	MP:0005556	abnormal renal filtration rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15141089
1558222	Kcnk5	potassium channel, subfamily K, member 5	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15141089
1558222	Kcnk5	potassium channel, subfamily K, member 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12707131
1558222	Kcnk5	potassium channel, subfamily K, member 5	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15141089
1558222	Kcnk5	potassium channel, subfamily K, member 5	gene	MP:0011406	abnormal retrotrapezoid nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133877
1558222	Kcnk5	potassium channel, subfamily K, member 5	gene	MP:0011459	increased urine chloride ion level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15141089
1558222	Kcnk5	potassium channel, subfamily K, member 5	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:20133877
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0000067	osteopetrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0000351	increased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802531
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802531
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802531
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0002724	enhanced wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802531
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802531
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0004982	abnormal osteoclast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0005076	abnormal cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464331
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20802531
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17464331
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558226	Jdp2	Jun dimerization protein 2	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23200825
1558227	Acot5	acyl-CoA thioesterase 5	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1558227	Acot5	acyl-CoA thioesterase 5	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20231207	MGI			
1558228	Cep70	centrosomal protein 70	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20240523	MGI			
1558228	Cep70	centrosomal protein 70	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0008279	arrest of spermiogenesis		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0009235	small sperm head		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0009239	short sperm flagellum		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558228	Cep70	centrosomal protein 70	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20230316	MGI			PMID:33980814
1558230	Bbln	bublin coiled coil protein	gene	MP:0000559	abnormal femur morphology		IAGP		N	RGD:5509061	20201210	MGI			PMID:32569872
1558230	Bbln	bublin coiled coil protein	gene	MP:0004984	increased osteoclast cell number		IAGP		N	RGD:5509061	20201210	MGI			PMID:32569872
1558230	Bbln	bublin coiled coil protein	gene	MP:0004992	increased bone resorption		IAGP		N	RGD:5509061	20201210	MGI			PMID:32569872
1558230	Bbln	bublin coiled coil protein	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20201210	MGI			PMID:32569872
1558230	Bbln	bublin coiled coil protein	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20201231	MGI			PMID:32569872
1558230	Bbln	bublin coiled coil protein	gene	MP:0010879	decreased trabecular bone volume		IAGP		N	RGD:5509061	20201231	MGI			PMID:32569872
1558230	Bbln	bublin coiled coil protein	gene	MP:0013630	increased bone trabecular spacing		IAGP		N	RGD:5509061	20201231	MGI			PMID:32569872
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0000733	abnormal muscle development		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0000751	myopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:9817932
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625552
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0001956	hypopnea		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9817932
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9817932
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0002279	abnormal diaphragm morphology		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0002280	abnormal intercostal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9817932
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:14625552
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0002841	impaired skeletal muscle contractility		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9817932
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0004232	decreased muscle weight		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0004701	decreased circulating insulin-like growth factor I level		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0005164	abnormal response to injury		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0005586	decreased tidal volume		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0009403	increased variability of skeletal muscle fiber size		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:9817932
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0009406	decreased skeletal muscle fiber number		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0009419	skeletal muscle fibrosis		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0009420	skeletal muscle endomysial fibrosis		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0010240	decreased skeletal muscle size		IAGP		N	RGD:5509061	20200409	MGI			PMID:28043812
1558231	Col6a1	collagen, type VI, alpha 1	gene	MP:0010938	decreased total lung capacity		IAGP		N	RGD:5509061	20260416	MGI			PMID:41287928
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0001004	abnormal retina photoreceptor morphology		IAGP		N	RGD:5509061	20150402	MGI			PMID:23745007
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0002090	abnormal vision		IAGP		N	RGD:5509061	20180222	MGI			PMID:25422369
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20150402	MGI			PMID:23745007
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20150402	MGI			PMID:23745007
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0005253	abnormal eye physiology		IAGP		N	RGD:5509061	20180222	MGI			PMID:25422369
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20150402	MGI			PMID:23745007
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20150402	MGI			PMID:23745007
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0008586	disorganized photoreceptor outer segment		IAGP		N	RGD:5509061	20150402	MGI			PMID:23745007
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0012029	abnormal electroretinogram waveform feature		IAGP		N	RGD:5509061	20180222	MGI			PMID:25422369
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0012031	abnormal b-wave amplitude		IAGP		N	RGD:5509061	20180222	MGI			PMID:25422369
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20180222	MGI			PMID:23745007
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20180222	MGI			PMID:25422369
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20180222	MGI			PMID:23745007
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20180222	MGI			PMID:25422369
1558232	Rp2	retinitis pigmentosa 2 homolog	gene	MP:0031606	increased susceptibility to age-related retinal degeneration		IAGP		N	RGD:5509061	20240404	MGI			PMID:25422369
1558236	Coro2b	coronin, actin binding protein, 2B	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1558236	Coro2b	coronin, actin binding protein, 2B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191219	MGI			PMID:31221975
1558236	Coro2b	coronin, actin binding protein, 2B	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20191219	MGI			PMID:31221975
1558236	Coro2b	coronin, actin binding protein, 2B	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20180329	MGI			PMID:29162887
1558236	Coro2b	coronin, actin binding protein, 2B	gene	MP:0006315	abnormal urine protein level		IAGP		N	RGD:5509061	20180329	MGI			PMID:29162887
1558236	Coro2b	coronin, actin binding protein, 2B	gene	MP:0014699	increased fibroblast adhesion		IAGP		N	RGD:5509061	20250710	MGI			PMID:29162887
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20240523	MGI			
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0003081	abnormal soleus morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0004088	abnormal sarcoplasmic reticulum morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0004089	dilated sarcoplasmic reticulum		IAGP		N	RGD:5509061	20251120	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0006267	abnormal intercalated disk morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0008842	lipofuscinosis		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0009141	increased prepulse inhibition		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0009710	anhedonia		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0010507	shortened RR interval		IEA		N	RGD:5509061	20240523	MGI			
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0010630	abnormal cardiac muscle tissue morphology		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0011749	perivascular fibrosis		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0020396	abnormal social recognition		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558237	Cmya5	cardiomyopathy associated 5	gene	MP:0020874	abnormal nervous system dopamine level		IAGP		N	RGD:5509061	20220428	MGI			PMID:34037836
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20210128	MGI			
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
1558238	Mef2b	myocyte enhancer factor 2B	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20200409	MGI			PMID:30205047
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0000183	decreased circulating LDL cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20201022	MGI			
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0002836	abnormal chorion morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20211021	MGI			
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20181227	MGI			
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20181227	MGI			
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558239	Wrap53	WD repeat containing, antisense to Trp53	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1558243	Iqcm	IQ motif containing M	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1558243	Iqcm	IQ motif containing M	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1558243	Iqcm	IQ motif containing M	gene	MP:0000642	enlarged adrenal glands		IEA		N	RGD:5509061	20241121	MGI			
1558243	Iqcm	IQ motif containing M	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20241121	MGI			
1558243	Iqcm	IQ motif containing M	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20241121	MGI			
1558243	Iqcm	IQ motif containing M	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1558243	Iqcm	IQ motif containing M	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20260402	MGI			
1558243	Iqcm	IQ motif containing M	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1558244	Ccdc18	coiled-coil domain containing 18	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20250508	MGI			
1558244	Ccdc18	coiled-coil domain containing 18	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20181227	MGI			
1558244	Ccdc18	coiled-coil domain containing 18	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20210128	MGI			
1558244	Ccdc18	coiled-coil domain containing 18	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20250508	MGI			
1558244	Ccdc18	coiled-coil domain containing 18	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1558244	Ccdc18	coiled-coil domain containing 18	gene	MP:0003443	increased circulating glycerol level		IEA		N	RGD:5509061	20211021	MGI			
1558244	Ccdc18	coiled-coil domain containing 18	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1558244	Ccdc18	coiled-coil domain containing 18	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1558245	Irf3	interferon regulatory factor 3	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1558245	Irf3	interferon regulatory factor 3	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210128	MGI			
1558245	Irf3	interferon regulatory factor 3	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20200130	MGI			PMID:31281243
1558245	Irf3	interferon regulatory factor 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20231207	MGI			
1558245	Irf3	interferon regulatory factor 3	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20231207	MGI			
1558245	Irf3	interferon regulatory factor 3	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20190523	MGI			PMID:28951494
1558245	Irf3	interferon regulatory factor 3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1558245	Irf3	interferon regulatory factor 3	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20201022	MGI			
1558245	Irf3	interferon regulatory factor 3	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20351692
1558245	Irf3	interferon regulatory factor 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20231207	MGI			
1558245	Irf3	interferon regulatory factor 3	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20201022	MGI			
1558245	Irf3	interferon regulatory factor 3	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070172
1558245	Irf3	interferon regulatory factor 3	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31281243
1558245	Irf3	interferon regulatory factor 3	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20200130	MGI			PMID:31281243
1558245	Irf3	interferon regulatory factor 3	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20190523	MGI			PMID:28951494
1558245	Irf3	interferon regulatory factor 3	gene	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20150212	MGI			PMID:19617565
1558245	Irf3	interferon regulatory factor 3	gene	MP:0008515	thin retina outer nuclear layer		IAGP		N	RGD:5509061	20200130	MGI			PMID:31281243
1558245	Irf3	interferon regulatory factor 3	gene	MP:0008518	retina outer nuclear layer degeneration		IAGP		N	RGD:5509061	20200130	MGI			PMID:31281243
1558245	Irf3	interferon regulatory factor 3	gene	MP:0008519	thin retina outer plexiform layer		IAGP		N	RGD:5509061	20200130	MGI			PMID:31281243
1558245	Irf3	interferon regulatory factor 3	gene	MP:0008548	abnormal circulating interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070172
1558245	Irf3	interferon regulatory factor 3	gene	MP:0008565	decreased interferon-beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20351692
1558245	Irf3	interferon regulatory factor 3	gene	MP:0008658	decreased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20351692
1558245	Irf3	interferon regulatory factor 3	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:30944222
1558245	Irf3	interferon regulatory factor 3	gene	MP:0011965	decreased total retina thickness		IAGP		N	RGD:5509061	20200130	MGI			PMID:31281243
1558245	Irf3	interferon regulatory factor 3	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20200130	MGI			PMID:31281243
1558245	Irf3	interferon regulatory factor 3	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20200130	MGI			PMID:31281243
1558245	Irf3	interferon regulatory factor 3	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20190523	MGI			PMID:28951494
1558245	Irf3	interferon regulatory factor 3	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:20351692
1558245	Irf3	interferon regulatory factor 3	gene	MP:0020937	increased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:11070172
1558245	Irf3	interferon regulatory factor 3	gene	MP:0020952	increased susceptibility to Paramyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:20351692
1558246	Sertad1	SERTA domain containing 1	gene	MP:0003059	decreased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20090907
1558246	Sertad1	SERTA domain containing 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20090907
1558246	Sertad1	SERTA domain containing 1	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:20090907
1558246	Sertad1	SERTA domain containing 1	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20090907
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0008167	increased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0008210	increased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558247	Bank1	B cell scaffold protein with ankyrin repeats 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16546095
1558248	Gas2	growth arrest specific 2	gene	MP:0001126	abnormal ovary morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0001130	abnormal ovarian folliculogenesis		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558248	Gas2	growth arrest specific 2	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0003582	abnormal ovary development		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0003825	abnormal pillar cell morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558248	Gas2	growth arrest specific 2	gene	MP:0004273	abnormal basal lamina morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0004300	abnormal organ of Corti supporting cell morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558248	Gas2	growth arrest specific 2	gene	MP:0004302	abnormal Deiters cell morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558248	Gas2	growth arrest specific 2	gene	MP:0004402	decreased cochlear outer hair cell number		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558248	Gas2	growth arrest specific 2	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558248	Gas2	growth arrest specific 2	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558248	Gas2	growth arrest specific 2	gene	MP:0008868	abnormal granulosa cell morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0009433	polyovular ovarian follicle		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20180719	MGI			PMID:27734842
1558248	Gas2	growth arrest specific 2	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20220616	MGI			PMID:33964205
1558249	Phldb2	pleckstrin homology like domain, family B, member 2	gene	MP:0001333	absent optic nerve		IEA		N	RGD:5509061	20200402	MGI			
1558249	Phldb2	pleckstrin homology like domain, family B, member 2	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20191107	MGI			PMID:30867511
1558249	Phldb2	pleckstrin homology like domain, family B, member 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210128	MGI			
1558249	Phldb2	pleckstrin homology like domain, family B, member 2	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1558249	Phldb2	pleckstrin homology like domain, family B, member 2	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20191107	MGI			PMID:30867511
1558249	Phldb2	pleckstrin homology like domain, family B, member 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30867511
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20191114	MGI			PMID:28747345
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20191114	MGI			PMID:28747345
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20240627	MGI			PMID:37316542
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20240627	MGI			PMID:37316542
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20240627	MGI			PMID:37316542
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0002531	abnormal type I hypersensitivity reaction		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0008764	increased mast cell degranulation		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20191114	MGI			PMID:28747345
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20240627	MGI			PMID:37316542
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0020116	increased sphingosine level		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0020116	increased sphingosine level		IAGP		N	RGD:5509061	20240627	MGI			PMID:37316542
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20230202	MGI			PMID:33643282
1558251	Ormdl3	ORM1-like 3 (S. cerevisiae)	gene	MP:0020582	increased ceramide level		IAGP		N	RGD:5509061	20240627	MGI			PMID:37316542
1558254	Lonrf2	LON peptidase N-terminal domain and ring finger 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20220519	MGI			
1558254	Lonrf2	LON peptidase N-terminal domain and ring finger 2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20220811	MGI			
1558254	Lonrf2	LON peptidase N-terminal domain and ring finger 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20220519	MGI			
1558254	Lonrf2	LON peptidase N-terminal domain and ring finger 2	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20210826	MGI			
1558254	Lonrf2	LON peptidase N-terminal domain and ring finger 2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20240523	MGI			
1558254	Lonrf2	LON peptidase N-terminal domain and ring finger 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1558256	Cldnd2	claudin domain containing 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20211021	MGI			
1558256	Cldnd2	claudin domain containing 2	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1558256	Cldnd2	claudin domain containing 2	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20211021	MGI			
1558256	Cldnd2	claudin domain containing 2	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1558256	Cldnd2	claudin domain containing 2	gene	MP:0011962	increased cornea thickness		IEA		N	RGD:5509061	20210128	MGI			
1558256	Cldnd2	claudin domain containing 2	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0000947	convulsive seizures		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0000951	sporadic seizures		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0001361	social withdrawal		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0001415	increased exploration in new environment		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20200402	MGI			PMID:30842726
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0002566	abnormal sexual interaction		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20200402	MGI			PMID:30842726
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0008428	abnormal spatial working memory		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0011987	abnormal GABAergic neuron physiology		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20200402	MGI			PMID:30842726
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0012348	decreased susceptibility to induction of seizure by inducing agent		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0012459	increased dentate gyrus size		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0020082	increased hippocampus volume		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0020351	decreased vocalization		IAGP		N	RGD:5509061	20200402	MGI			PMID:31978606
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20200402	MGI			PMID:30842726
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0020573	abnormal corpus callosum size		IAGP		N	RGD:5509061	20200310	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:30842726
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:31439632
1558257	Iqsec2	IQ motif and Sec7 domain 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:31978606
1558258	Nap1l2	nucleosome assembly protein 1-like 2	gene	MP:0002151	abnormal neural tube morphology		IEA		N	RGD:5509061	20141003	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20221215	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210128	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:20634410
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20210128	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20200514	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20241121	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0002804	abnormal motor learning		IAGP		N	RGD:5509061	20200310	MGI			PMID:20634410
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0002894	abnormal otolith morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200514	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0002978	absent otoliths		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0003143	enlarged otoliths		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20241121	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0004330	abnormal vestibular saccular macula morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20221215	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0005191	head tilt		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20221215	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20211021	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0006090	abnormal utricle morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210128	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0009979	abnormal cerebellum deep nucleus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20634410
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20241121	MGI			
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:20634410
1558262	Atg4b	autophagy related 4B, cysteine peptidase	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:20577052
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20241121	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20191128	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20191128	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20191128	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0001730	embryonic growth arrest		IEA		N	RGD:5509061	20191205	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20191128	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20191128	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20190502	MGI			
1558263	Tpk1	thiamine pyrophosphokinase	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0003983	decreased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18573875
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558265	Inpp5k	inositol polyphosphate 5-phosphatase K	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:18573875
1558266	Fut2b	fucosyltransferase 2B	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20220804	MGI			PMID:35696408
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0000135	decreased compact bone thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792071
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0003026	decreased vasoconstriction		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0004991	decreased bone strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:22792071
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0005595	abnormal vascular smooth muscle physiology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0009862	abnormal aorta elastic tissue morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0009865	abnormal aorta smooth muscle morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0009867	abnormal ascending aorta morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0014342	abnormal muscle fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0021182	decreased femoral compact bone area		IAGP		N	RGD:5509061	20220922	MGI			PMID:22792071
1558269	Wnt16	wingless-type MMTV integration site family, member 16	gene	MP:0031274	increased susceptibility to induced aneurysm formation		IAGP		N	RGD:5509061	20250227	MGI			PMID:38123514
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923441
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923441
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923441
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923441
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923441
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923441
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923441
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:11923441
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0004156	abnormal QT variability		IEA		N	RGD:5509061	20230601	MGI			
1558270	Aff2	AF4/FMR2 family, member 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20240523	MGI			
1558271	Zcchc2	zinc finger, CCHC domain containing 2	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20230601	MGI			
1558271	Zcchc2	zinc finger, CCHC domain containing 2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20240523	MGI			
1558271	Zcchc2	zinc finger, CCHC domain containing 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20230601	MGI			
1558271	Zcchc2	zinc finger, CCHC domain containing 2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20240523	MGI			
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0003233	prolonged QT interval		IEA		N	RGD:5509061	20220811	MGI			
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220519	MGI			
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20230601	MGI			
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220519	MGI			
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220519	MGI			
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0014630	abnormal round spermatid morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0030980	abnormal acroplaxome morphology		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558272	Ssh2	slingshot protein phosphatase 2	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20260129	MGI			PMID:36942942
1558274	2610028H24Rik	RIKEN cDNA 2610028H24 gene	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1558274	2610028H24Rik	RIKEN cDNA 2610028H24 gene	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20240523	MGI			
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18232732
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:11283248
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:18232732
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0014946	abnormal muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:11283248
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0014970	decreased muscle enzyme/coenzyme activity		IAGP		N	RGD:5509061	20260409	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0020411	increased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20170803	MGI			PMID:12606498
1558275	Ppp1r3a	protein phosphatase 1, regulatory subunit 3A	gene	MP:0031618	decreased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:12606498
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0003978	decreased circulating carnitine level		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0009125	decreased brown fat cell lipid droplet size		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0009643	abnormal urine homeostasis		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0011049	impaired adaptive thermogenesis		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20151112	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0031115	macrovesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21659959
1558276	Acad8	acyl-Coenzyme A dehydrogenase family, member 8	gene	MP:0031116	microvesicular hepatic steatosis		IAGP		N	RGD:5509061	20200917	MGI			PMID:21659959
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20161201	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210128	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20260402	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20161201	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20260402	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20240523	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20230119	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0002834	decreased heart weight		IEA		N	RGD:5509061	20161201	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20240523	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20230119	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20230119	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210128	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20240523	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230119	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20161201	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20230119	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0011952	decreased cardiac stroke volume		IEA		N	RGD:5509061	20260402	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20230119	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0011971	increased circulating lactate dehydrogenase level		IEA		N	RGD:5509061	20211021	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0013510	decreased CD4-negative NK T cell number		IEA		N	RGD:5509061	20230119	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0013669	decreased Ly6C-positive immature NK cell number		IEA		N	RGD:5509061	20230119	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0013678	decreased Ly6C-positive NK T cell number		IEA		N	RGD:5509061	20230119	MGI			
1558277	Ube3c	ubiquitin protein ligase E3C	gene	MP:0013691	decreased CD5-positive Ly6C-positive T cell number		IEA		N	RGD:5509061	20230119	MGI			
1558278	Rnase12	ribonuclease, RNase A family, 12 (non-active)	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20201022	MGI			
1558278	Rnase12	ribonuclease, RNase A family, 12 (non-active)	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20201022	MGI			
1558279	Hoxc4	homeobox C4	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626021
1558279	Hoxc4	homeobox C4	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363484
1558279	Hoxc4	homeobox C4	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363484
1558279	Hoxc4	homeobox C4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660891
1558279	Hoxc4	homeobox C4	gene	MP:0002492	decreased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363484
1558279	Hoxc4	homeobox C4	gene	MP:0002823	abnormal rib development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626021
1558279	Hoxc4	homeobox C4	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626021
1558279	Hoxc4	homeobox C4	gene	MP:0003047	abnormal thoracic vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660891
1558279	Hoxc4	homeobox C4	gene	MP:0003159	abnormal esophageal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660891
1558279	Hoxc4	homeobox C4	gene	MP:0004323	sternum hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660891
1558279	Hoxc4	homeobox C4	gene	MP:0004618	thoracic vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660891
1558279	Hoxc4	homeobox C4	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660891
1558279	Hoxc4	homeobox C4	gene	MP:0004679	xiphoid process foramen		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626021
1558279	Hoxc4	homeobox C4	gene	MP:0004815	abnormal somatic hypermutation frequency		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363484
1558279	Hoxc4	homeobox C4	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363484
1558279	Hoxc4	homeobox C4	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626021
1558279	Hoxc4	homeobox C4	gene	MP:0008148	abnormal sternocostal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660891
1558279	Hoxc4	homeobox C4	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363484
1558279	Hoxc4	homeobox C4	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363484
1558279	Hoxc4	homeobox C4	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363484
1558279	Hoxc4	homeobox C4	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363484
1558279	Hoxc4	homeobox C4	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660891
1558279	Hoxc4	homeobox C4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:8660891
1558279	Hoxc4	homeobox C4	gene	MP:0012284	increased sternebra number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8626021
1558280	Vwa2	von Willebrand factor A domain containing 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1558281	Gimap7	GTPase, IMAP family member 7	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20240523	MGI			
1558281	Gimap7	GTPase, IMAP family member 7	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20241121	MGI			
1558281	Gimap7	GTPase, IMAP family member 7	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20241121	MGI			
1558281	Gimap7	GTPase, IMAP family member 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1558283	Lyg1	lysozyme G-like 1	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20190912	MGI			PMID:28507796
1558283	Lyg1	lysozyme G-like 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190912	MGI			PMID:28507796
1558283	Lyg1	lysozyme G-like 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20190912	MGI			PMID:28507796
1558283	Lyg1	lysozyme G-like 1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20190912	MGI			PMID:28507796
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0001182	lung hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0002672	abnormal pharyngeal arch artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0003105	abnormal heart atrium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0003542	abnormal vascular endothelial cell development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0003659	abnormal lymph circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0004038	lymphangiectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0004787	abnormal dorsal aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0005244	hemopericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20221215	MGI			
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0010195	abnormal lymphatic vessel endothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22898778
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0012080	chylous ascites		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0012511	dilated aortic sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151727
1558285	Heg1	heart development protein with EGF-like domains 1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:22898778
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20210520	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0000559	abnormal femur morphology		IEA		N	RGD:5509061	20160804	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20190502	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20190808	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20160811	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20200514	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20200514	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20190502	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20230601	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20190808	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0002311	abnormal inspiratory capacity		IEA		N	RGD:5509061	20200514	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20200514	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20230601	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20230601	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20240523	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20160804	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0003020	decreased circulating chloride level		IEA		N	RGD:5509061	20210128	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20250508	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0003393	decreased cardiac output		IEA		N	RGD:5509061	20190502	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IEA		N	RGD:5509061	20210826	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0003929	decreased heart rate variability		IEA		N	RGD:5509061	20210826	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20210826	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20200514	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20211021	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20210128	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:5509061	20210826	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20141003	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20210128	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20170105	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20230601	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20211021	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:23870131
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20170105	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20250508	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0009454	impaired contextual conditioning behavior		IEA		N	RGD:5509061	20231207	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160811	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0010090	increased circulating creatine kinase level		IEA		N	RGD:5509061	20211021	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20161201	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0010895	increased lung compliance		IEA		N	RGD:5509061	20200514	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20190502	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20160421	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0020420	abnormal freezing behavior		IEA		N	RGD:5509061	20211021	MGI			
1558286	Ap4e1	adaptor-related protein complex AP-4, epsilon 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20210128	MGI			
1558287	Adam5	a disintegrin and metallopeptidase domain 5	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20260625	MGI			PMID:41263505
1558287	Adam5	a disintegrin and metallopeptidase domain 5	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1558287	Adam5	a disintegrin and metallopeptidase domain 5	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1558287	Adam5	a disintegrin and metallopeptidase domain 5	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20260625	MGI			PMID:41263505
1558287	Adam5	a disintegrin and metallopeptidase domain 5	gene	MP:0014696	decreased cell adhesion		IAGP		N	RGD:5509061	20260625	MGI			PMID:41263505
1558287	Adam5	a disintegrin and metallopeptidase domain 5	gene	MP:0014788	decreased protein level		IAGP		N	RGD:5509061	20260625	MGI			PMID:41263505
1558287	Adam5	a disintegrin and metallopeptidase domain 5	gene	MP:0030978	impaired binding of sperm to zona pellucida		IAGP		N	RGD:5509061	20260625	MGI			PMID:41263505
1558287	Adam5	a disintegrin and metallopeptidase domain 5	gene	MP:0031012	impaired sperm migration in female genital tract		IAGP		N	RGD:5509061	20260625	MGI			PMID:41263505
1558288	Aspn	asporin	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20190502	MGI			
1558288	Aspn	asporin	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1558288	Aspn	asporin	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1558288	Aspn	asporin	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20231221	MGI			PMID:28859141
1558288	Aspn	asporin	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1558288	Aspn	asporin	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1558288	Aspn	asporin	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1558288	Aspn	asporin	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1558288	Aspn	asporin	gene	MP:0005275	abnormal skin tensile strength		IAGP		N	RGD:5509061	20231221	MGI			PMID:28859141
1558288	Aspn	asporin	gene	MP:0008438	abnormal cutaneous collagen fibril morphology		IAGP		N	RGD:5509061	20231221	MGI			PMID:28859141
1558288	Aspn	asporin	gene	MP:0011475	abnormal glycosaminoglycan level		IAGP		N	RGD:5509061	20231221	MGI			PMID:28859141
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697838
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0000359	abnormal mast cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645152
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697838
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0000491	crypts of Lieberkuhn abscesses		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697838
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726392
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10544204
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22079330
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002223	lymphoid hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10544204
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730112
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002408	abnormal double-positive T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23305739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645152
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11070165
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002455	abnormal dendritic cell antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807484
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11493455
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22079330
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22079330
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22079330
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697838
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002827	abnormal renal corpuscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22079330
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645152
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0003091	abnormal cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12730112
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10544204
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697838
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10544204
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697838
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10544204
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697838
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10544204
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697838
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10544204
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12807484
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9697838
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005153	abnormal B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008082	increased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17878299
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22302739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0008396	abnormal osteoclast differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14726392
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0011339	abnormal glomerular mesangium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22079330
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20141003	MGI			PMID:22079330
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0011427	increased mesangial cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22079330
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20180125	MGI			PMID:22079330
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0031723	abnormal podosome assembly		IAGP		N	RGD:5509061	20260507	MGI			PMID:19805221
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0031723	abnormal podosome assembly		IAGP		N	RGD:5509061	20260507	MGI			PMID:23305739
1558289	Was	Wiskott-Aldrich syndrome	gene	MP:0031725	abnormal podosome physiology		IAGP		N	RGD:5509061	20260507	MGI			PMID:19805221
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0001693	failure of primitive streak formation		IEA		N	RGD:5509061	20240919	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0001696	failure to gastrulate		IEA		N	RGD:5509061	20240919	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0001698	decreased embryo size		IEA		N	RGD:5509061	20240919	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210128	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0009331	absent primitive node		IEA		N	RGD:5509061	20240919	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0012724	absent head fold		IEA		N	RGD:5509061	20240919	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20210128	MGI			
1558290	Hars2	histidyl-tRNA synthetase 2	gene	MP:0014586	decreased egg cylinder size		IEA		N	RGD:5509061	20241212	MGI			
1558291	Snx27	sorting nexin family member 27	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20221215	MGI			
1558291	Snx27	sorting nexin family member 27	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20190808	MGI			
1558291	Snx27	sorting nexin family member 27	gene	MP:0000477	abnormal intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300787
1558291	Snx27	sorting nexin family member 27	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300787
1558291	Snx27	sorting nexin family member 27	gene	MP:0000692	small spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300787
1558291	Snx27	sorting nexin family member 27	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300787
1558291	Snx27	sorting nexin family member 27	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1558291	Snx27	sorting nexin family member 27	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300787
1558291	Snx27	sorting nexin family member 27	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20211021	MGI			
1558291	Snx27	sorting nexin family member 27	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1558291	Snx27	sorting nexin family member 27	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300787
1558291	Snx27	sorting nexin family member 27	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300787
1558291	Snx27	sorting nexin family member 27	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300787
1558291	Snx27	sorting nexin family member 27	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21300787
1558291	Snx27	sorting nexin family member 27	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558293	Zc3h7a	zinc finger CCCH type containing 7 A	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1558293	Zc3h7a	zinc finger CCCH type containing 7 A	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1558293	Zc3h7a	zinc finger CCCH type containing 7 A	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1558293	Zc3h7a	zinc finger CCCH type containing 7 A	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20240523	MGI			
1558293	Zc3h7a	zinc finger CCCH type containing 7 A	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1558293	Zc3h7a	zinc finger CCCH type containing 7 A	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220519	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0000556	abnormal hindlimb morphology		IEA		N	RGD:5509061	20240523	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20220811	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0002626	increased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210826	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210520	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0005470	increased thyroxine level		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0005473	decreased triiodothyronine level		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0005632	decreased circulating aspartate transaminase level		IEA		N	RGD:5509061	20210826	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0005655	increased aggression		IEA		N	RGD:5509061	20220811	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0009808	decreased oligodendrocyte number		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210826	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210826	MGI			
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0011731	decreased myelin sheath thickness		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1558294	Secisbp2l	SECIS binding protein 2-like	gene	MP:0014318	abnormal oligodendrocyte differentiation		IAGP		N	RGD:5509061	20241017	MGI			PMID:35760530
1558295	Amot	angiomotin	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699752
1558295	Amot	angiomotin	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699752
1558295	Amot	angiomotin	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676095
1558295	Amot	angiomotin	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676095
1558295	Amot	angiomotin	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699752
1558295	Amot	angiomotin	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699752
1558295	Amot	angiomotin	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676095
1558295	Amot	angiomotin	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699752
1558295	Amot	angiomotin	gene	MP:0004938	dilated vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699752
1558295	Amot	angiomotin	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699752
1558295	Amot	angiomotin	gene	MP:0011106	embryonic lethality between implantation and somite formation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676095
1558295	Amot	angiomotin	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17699752
1558295	Amot	angiomotin	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676095
1558295	Amot	angiomotin	gene	MP:0011255	abnormal anterior visceral endoderm cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12676095
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20210520	MGI			
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0000649	sebaceous gland atrophy		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001212	skin lesions		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001310	abnormal conjunctiva morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:34113821
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001314	cornea opacity		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001322	abnormal iris morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001337	dry eyes		IAGP		N	RGD:5509061	20221117	MGI			PMID:34113821
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001340	abnormal eyelid morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001349	excessive tearing		IAGP		N	RGD:5509061	20221117	MGI			PMID:34113821
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001851	eye inflammation		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210520	MGI			
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0001994	increased blinking frequency		IAGP		N	RGD:5509061	20221117	MGI			PMID:34113821
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20260402	MGI			
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0004222	iris synechia		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0005252	abnormal Meibomian gland morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0005252	abnormal Meibomian gland morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:34113821
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0005300	abnormal cornea stroma morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20221215	MGI			
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0005542	cornea vascularization		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0006000	abnormal cornea epithelium morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0006193	conjunctival telangiectasia		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0006203	eye hemorrhage		IEA		N	RGD:5509061	20210128	MGI			
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0008778	abnormal lymphangiogenesis		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0009935	abnormal Meibomian gland acinus morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0010202	focal dorsal hair loss		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0010699	dilated hair follicle		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0013145	eye discharge		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0013192	decreased sebaceous gland number		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0013375	abnormal sebocyte morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0013386	enlarged Meibomian gland		IAGP		N	RGD:5509061	20221117	MGI			PMID:34113821
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0013391	abnormal Meibomian gland physiology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0013391	abnormal Meibomian gland physiology		IAGP		N	RGD:5509061	20221117	MGI			PMID:34113821
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0014131	abnormal tear film morphology		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0014131	abnormal tear film morphology		IAGP		N	RGD:5509061	20221117	MGI			PMID:34113821
1558296	Awat2	acyl-CoA wax alcohol acyltransferase 2	gene	MP:0014154	Meibomian gland degeneration		IAGP		N	RGD:5509061	20210819	MGI			PMID:32851726
1558297	Prss50	serine protease 50	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
1558297	Prss50	serine protease 50	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20160804	MGI			
1558297	Prss50	serine protease 50	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20160804	MGI			
1558297	Prss50	serine protease 50	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20141003	MGI			
1558297	Prss50	serine protease 50	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0009282	decreased hyperactivated sperm motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20210603	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0009839	multiflagellated sperm		IAGP		N	RGD:5509061	20220630	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220714	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20220714	MGI			PMID:33913480
1558297	Prss50	serine protease 50	gene	MP:0031408	multi-headed sperm		IAGP		N	RGD:5509061	20220630	MGI			PMID:33913480
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0000255	blood vessel congestion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0001327	decreased retina photoreceptor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0001328	disorganized retina layers		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837032
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0002855	abnormal cochlear ganglion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0002857	cochlear ganglion degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0003070	increased vascular permeability		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0003728	abnormal retina photoreceptor layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0003732	abnormal retina outer plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0003733	abnormal retina inner nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004363	stria vascularis degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004367	abnormal strial intermediate cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004368	abnormal stria vascularis vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004487	type I spiral ligament fibrocyte degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004740	sensorineural hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004748	increased susceptibility to age-related hearing loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004758	absent strial marginal cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0004950	abnormal brain vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19837032
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0006200	vitreous body deposition		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0008509	disorganized retina ganglion layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0008584	photoreceptor outer segment degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:8789439
1558298	Ndp	Norrie disease (pseudoglioma) (human)	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12040033
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17124501
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0000861	disorganized barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525048
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:17124501
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17124501
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0001386	abnormal maternal nurturing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11797009
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11797010
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0001898	abnormal long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:11797010
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525048
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074017
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074017
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21241895
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:11797009
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16525048
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:11797009
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17124501
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002918	abnormal paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11797009
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11797009
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074017
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002920	decreased paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11797009
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002921	abnormal post-tetanic potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11797009
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074017
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21241895
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0004807	abnormal paired-pulse inhibition		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074017
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21241895
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0004835	abnormal miniature endplate potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:17124501
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0005112	abnormal spinal cord ventral horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17124501
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0005192	increased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17124501
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0010104	enlarged thoracic cage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17124501
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19074017
1558300	Rims1	regulating synaptic membrane exocytosis 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17124501
1558305	Gmip	Gem-interacting protein	gene	MP:0010088	decreased circulating fructosamine level		IEA		N	RGD:5509061	20210128	MGI			
1558307	Cd160	CD160 antigen	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200723	MGI			PMID:32231122
1558307	Cd160	CD160 antigen	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20160128	MGI			PMID:25711213
1558307	Cd160	CD160 antigen	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20160128	MGI			PMID:25711213
1558308	Nhlrc3	NHL repeat containing 3	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1558308	Nhlrc3	NHL repeat containing 3	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1558308	Nhlrc3	NHL repeat containing 3	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1558310	C1ql3	C1q-like 3	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1558310	C1ql3	C1q-like 3	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1558310	C1ql3	C1q-like 3	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20161020	MGI			PMID:27478018
1558310	C1ql3	C1q-like 3	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20161020	MGI			PMID:27478018
1558310	C1ql3	C1q-like 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20161020	MGI			PMID:27478018
1558310	C1ql3	C1q-like 3	gene	MP:0002805	abnormal conditioned taste aversion behavior		IAGP		N	RGD:5509061	20161020	MGI			PMID:27478018
1558310	C1ql3	C1q-like 3	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1558310	C1ql3	C1q-like 3	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20230601	MGI			
1558310	C1ql3	C1q-like 3	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1558310	C1ql3	C1q-like 3	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20161020	MGI			PMID:27478018
1558310	C1ql3	C1q-like 3	gene	MP:0009456	impaired cued conditioning behavior		IAGP		N	RGD:5509061	20161020	MGI			PMID:27478018
1558310	C1ql3	C1q-like 3	gene	MP:0009712	impaired conditioned place preference behavior		IAGP		N	RGD:5509061	20161020	MGI			PMID:27478018
1558310	C1ql3	C1q-like 3	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20161020	MGI			PMID:27478018
1558311	Cyp2b10	cytochrome P450, family 2, subfamily b, polypeptide 10	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20231019	MGI			PMID:36224745
1558311	Cyp2b10	cytochrome P450, family 2, subfamily b, polypeptide 10	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20231019	MGI			PMID:36224745
1558311	Cyp2b10	cytochrome P450, family 2, subfamily b, polypeptide 10	gene	MP:0005443	abnormal ethanol metabolism		IAGP		N	RGD:5509061	20231019	MGI			PMID:36224745
1558311	Cyp2b10	cytochrome P450, family 2, subfamily b, polypeptide 10	gene	MP:0009642	abnormal blood homeostasis		IAGP		N	RGD:5509061	20231019	MGI			PMID:36224745
1558311	Cyp2b10	cytochrome P450, family 2, subfamily b, polypeptide 10	gene	MP:0010951	abnormal lipid oxidation		IAGP		N	RGD:5509061	20231019	MGI			PMID:36224745
1558311	Cyp2b10	cytochrome P450, family 2, subfamily b, polypeptide 10	gene	MP:0031267	increased susceptibility to alcohol-induced hepatic steatosis		IAGP		N	RGD:5509061	20231019	MGI			PMID:36224745
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0000493	rectal prolapse		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001302	eyelids open at birth		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001349	excessive tearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001412	excessive scratching		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:12815074
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0003868	abnormal feces composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0005034	abnormal anus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0006167	eyelid edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0009859	eye opacity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809813
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12815074
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12815074
1558312	Rad23b	RAD23 homolog B, nucleotide excision repair protein	gene	MP:0014762	impaired base-excision repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:12815074
1558313	Ninl	ninein-like	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1558313	Ninl	ninein-like	gene	MP:0013415	increased myeloid cell number in bone marrow		IAGP		N	RGD:5509061	20160915	MGI			PMID:24652767
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0001183	overexpanded pulmonary alveolus		IAGP		N	RGD:5509061	20180412	MGI			PMID:28145888
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20180412	MGI			PMID:28145888
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20180412	MGI			PMID:28145888
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20150430	MGI			
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0001919	abnormal reproductive system physiology		IEA		N	RGD:5509061	20141003	MGI			
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0001942	abnormal lung volume		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20231207	MGI			
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20231207	MGI			
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20220811	MGI			
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20180412	MGI			PMID:28145888
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20180412	MGI			PMID:28145888
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0005642	decreased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20231207	MGI			
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20180412	MGI			PMID:28145888
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20180412	MGI			PMID:28145888
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0009571	abnormal right lung accessory lobe morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0010975	abnormal lung lobe morphology		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0011024	abnormal branching involved in lung morphogenesis		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0011289	abnormal nephron number		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0011493	double ureter		IAGP		N	RGD:5509061	20191205	MGI			PMID:31242448
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20180412	MGI			PMID:28145888
1558314	Adamts18	ADAM metallopeptidase with thrombospondin type 1 motif 18	gene	MP:0014222	decreased colon goblet cell number		IAGP		N	RGD:5509061	20180412	MGI			PMID:28145888
1558319	Zfp786	zinc finger protein 786	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1558320	Cldn2	claudin 2	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385797
1558320	Cldn2	claudin 2	gene	MP:0002988	decreased urine osmolality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385797
1558320	Cldn2	claudin 2	gene	MP:0004041	increased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20170713	MGI			PMID:27214555
1558320	Cldn2	claudin 2	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20170713	MGI			PMID:27214555
1558320	Cldn2	claudin 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20170713	MGI			PMID:27214555
1558320	Cldn2	claudin 2	gene	MP:0005441	increased urine calcium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385797
1558320	Cldn2	claudin 2	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20170713	MGI			PMID:27214555
1558320	Cldn2	claudin 2	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20170713	MGI			PMID:27214555
1558320	Cldn2	claudin 2	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385797
1558320	Cldn2	claudin 2	gene	MP:0006316	increased urine sodium level		IAGP		N	RGD:5509061	20170713	MGI			PMID:27214555
1558320	Cldn2	claudin 2	gene	MP:0010107	abnormal renal reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385797
1558320	Cldn2	claudin 2	gene	MP:0010108	abnormal renal water reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385797
1558320	Cldn2	claudin 2	gene	MP:0010109	abnormal renal sodium reabsorption		IAGP		N	RGD:5509061	20141003	MGI			PMID:20385797
1558320	Cldn2	claudin 2	gene	MP:0010109	abnormal renal sodium reabsorption		IAGP		N	RGD:5509061	20170713	MGI			PMID:27214555
1558320	Cldn2	claudin 2	gene	MP:0011442	abnormal renal sodium ion transport		IAGP		N	RGD:5509061	20170713	MGI			PMID:27214555
1558320	Cldn2	claudin 2	gene	MP:0014781	decreased kidney enzyme/coenzyme level		IAGP		N	RGD:5509061	20251030	MGI			PMID:27214555
1558321	Lrrc25	leucine rich repeat containing 25	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20210415	MGI			PMID:30340835
1558321	Lrrc25	leucine rich repeat containing 25	gene	MP:0001853	heart inflammation		IAGP		N	RGD:5509061	20210415	MGI			PMID:30340835
1558321	Lrrc25	leucine rich repeat containing 25	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20210415	MGI			PMID:30340835
1558321	Lrrc25	leucine rich repeat containing 25	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20210415	MGI			PMID:30340835
1558321	Lrrc25	leucine rich repeat containing 25	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20210415	MGI			PMID:30340835
1558321	Lrrc25	leucine rich repeat containing 25	gene	MP:0008837	increased transforming growth factor beta level		IAGP		N	RGD:5509061	20210415	MGI			PMID:30340835
1558321	Lrrc25	leucine rich repeat containing 25	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:30340835
1558322	Sp9	trans-acting transcription factor 9	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20180705	MGI			PMID:27452460
1558322	Sp9	trans-acting transcription factor 9	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20180705	MGI			PMID:27452460
1558322	Sp9	trans-acting transcription factor 9	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20180705	MGI			PMID:27452460
1558322	Sp9	trans-acting transcription factor 9	gene	MP:0004077	abnormal striatum morphology		IAGP		N	RGD:5509061	20180705	MGI			PMID:27452460
1558322	Sp9	trans-acting transcription factor 9	gene	MP:0008462	abnormal medium spiny neuron morphology		IAGP		N	RGD:5509061	20180705	MGI			PMID:27452460
1558322	Sp9	trans-acting transcription factor 9	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20180705	MGI			PMID:27452460
1558322	Sp9	trans-acting transcription factor 9	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20180705	MGI			PMID:27452460
1558322	Sp9	trans-acting transcription factor 9	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20180705	MGI			PMID:27452460
1558322	Sp9	trans-acting transcription factor 9	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:27452460
1558327	Cnih4	cornichon family AMPA receptor auxiliary protein 4	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20230309	MGI			PMID:36657507
1558327	Cnih4	cornichon family AMPA receptor auxiliary protein 4	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20230309	MGI			PMID:36657507
1558327	Cnih4	cornichon family AMPA receptor auxiliary protein 4	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20230309	MGI			PMID:36657507
1558328	Dnaaf9	dynein axonemal assembly factor 9	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20231207	MGI			
1558328	Dnaaf9	dynein axonemal assembly factor 9	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20210826	MGI			
1558331	Serpina6	serine (or cysteine) peptidase inhibitor, clade A, member 6	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980625
1558331	Serpina6	serine (or cysteine) peptidase inhibitor, clade A, member 6	gene	MP:0002573	behavioral despair		IAGP		N	RGD:5509061	20141003	MGI			PMID:20022933
1558331	Serpina6	serine (or cysteine) peptidase inhibitor, clade A, member 6	gene	MP:0005129	increased adrenocorticotropin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980625
1558331	Serpina6	serine (or cysteine) peptidase inhibitor, clade A, member 6	gene	MP:0005345	abnormal circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980625
1558331	Serpina6	serine (or cysteine) peptidase inhibitor, clade A, member 6	gene	MP:0005345	abnormal circulating corticosterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20022933
1558331	Serpina6	serine (or cysteine) peptidase inhibitor, clade A, member 6	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980625
1558331	Serpina6	serine (or cysteine) peptidase inhibitor, clade A, member 6	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980625
1558331	Serpina6	serine (or cysteine) peptidase inhibitor, clade A, member 6	gene	MP:0009758	impaired behavioral response to cocaine		IAGP		N	RGD:5509061	20141003	MGI			PMID:20022933
1558331	Serpina6	serine (or cysteine) peptidase inhibitor, clade A, member 6	gene	MP:0010210	abnormal circulating cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16980625
1558332	H2-T23	histocompatibility 2, T region locus 23	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20180719	MGI			PMID:15098030
1558332	H2-T23	histocompatibility 2, T region locus 23	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20180719	MGI			PMID:15098030
1558332	H2-T23	histocompatibility 2, T region locus 23	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:15098030
1558332	H2-T23	histocompatibility 2, T region locus 23	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:19047627
1558332	H2-T23	histocompatibility 2, T region locus 23	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20180719	MGI			PMID:19047627
1558332	H2-T23	histocompatibility 2, T region locus 23	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17509909
1558332	H2-T23	histocompatibility 2, T region locus 23	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:19047627
1558332	H2-T23	histocompatibility 2, T region locus 23	gene	MP:0008051	abnormal memory T cell physiology		IAGP		N	RGD:5509061	20180719	MGI			PMID:17509909
1558332	H2-T23	histocompatibility 2, T region locus 23	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:15098030
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0001889	delayed brain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0002027	increased lung adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0004188	delayed embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20210128	MGI			
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0008642	decreased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0009782	abnormal basicranium angle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0010208	prognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20190912	MGI			PMID:29539633
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0013504	increased embryonic tissue cell apoptosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:20566848
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20230608	MGI			PMID:23277562
1558333	Smg1	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	gene	MP:0030241	absent optic pit		IAGP		N	RGD:5509061	20171109	MGI			PMID:20566848
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20181227	MGI			
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386003
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20260402	MGI			
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:22976293
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0001785	edema		IEA		N	RGD:5509061	20210520	MGI			
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386003
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22976293
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386003
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18188447
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855869
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0002886	abnormal glutamate-mediated receptor currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386003
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0002916	increased synaptic depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386003
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386003
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220519	MGI			
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386003
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20141003	MGI			PMID:22976293
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855869
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855869
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372168
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22976293
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855869
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855869
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0008687	increased interleukin-2 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20855869
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0008788	abnormal fetal cardiomyocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386003
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20141003	MGI			PMID:22976293
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0009548	abnormal platelet aggregation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23372168
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15386003
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22976293
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17609388
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558334	Pip5k1c	phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma	gene	MP:0014553	decreased neuronal migration		IAGP		N	RGD:5509061	20241121	MGI			PMID:17609388
1558335	Derl3	Der1-like domain family, member 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11422294
1558336	Ngdn	neuroguidin, EIF4E binding protein	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20211021	MGI			
1558336	Ngdn	neuroguidin, EIF4E binding protein	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20220811	MGI			
1558336	Ngdn	neuroguidin, EIF4E binding protein	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20181227	MGI			
1558336	Ngdn	neuroguidin, EIF4E binding protein	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530702
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0002220	large lymphoid organs		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0002418	increased susceptibility to viral infection		IAGP		N	RGD:5509061	20221222	MGI			PMID:35266071
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20221222	MGI			PMID:35266071
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530702
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530702
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0005079	decreased cytotoxic T cell cytolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0008076	abnormal CD4-positive T cell differentiation		IAGP		N	RGD:5509061	20221229	MGI			PMID:35266071
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20221222	MGI			PMID:35266071
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20221222	MGI			PMID:35266071
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20221222	MGI			PMID:35266071
1558337	Elf4	E74 like ETS transcription factor 4	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12387738
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000522	kidney cortex cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9568711
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000531	right pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307093
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000596	abnormal liver development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307093
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000650	mesocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001270	distended abdomen		IEA		N	RGD:5509061	20151112	MGI			
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307093
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307093
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0001944	abnormal pancreas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002058	neonatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20151203	MGI			PMID:25574838
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307093
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002705	dilated renal tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002767	situs ambiguus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003231	abnormal placenta vasculature		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003253	dilated bile duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003255	bile duct proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9568711
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9568711
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003327	liver cyst		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003336	pancreas cyst		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003606	kidney failure		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:12140187
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18235088
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20181743
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9568711
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003675	kidney cyst		IAGP		N	RGD:5509061	20210603	MGI			PMID:28750036
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20151203	MGI			PMID:25574838
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0004020	polyhydramnios		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301212
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0004020	polyhydramnios		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12859898
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0004066	abnormal primitive node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23357539
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0004190	abnormal direction of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307093
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0004860	dilated kidney collecting duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959710
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0005553	increased circulating creatinine level		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0005554	decreased circulating creatinine level		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21685914
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20151203	MGI			PMID:25574838
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0005565	increased blood urea nitrogen level		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:9568711
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20151203	MGI			PMID:25574838
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301212
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0009050	dilated proximal convoluted tubule		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0009144	dilated pancreatic duct		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0009760	abnormal mitotic spindle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19959710
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0010439	abnormal hepatic vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0010807	abnormal stomach position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19235720
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0010808	right-sided stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307093
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12062060
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10615132
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20181743
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21307093
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23357539
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20862291
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23357539
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011307	kidney medulla cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:9568711
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011331	abnormal papillary duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011368	increased kidney apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20181129	MGI			PMID:28244683
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011440	increased kidney cell proliferation		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011441	decreased kidney cell proliferation		IAGP		N	RGD:5509061	20190725	MGI			PMID:28205547
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0011501	increased glomerular capsule space		IAGP		N	RGD:5509061	20141003	MGI			PMID:18782757
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0012172	abnormal amniotic fluid composition		IAGP		N	RGD:5509061	20141003	MGI			PMID:16301212
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0012236	abnormal cholangiocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0012237	increased cholangiocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558338	Pkd2	polycystin 2, transient receptor potential cation channel	gene	MP:0012238	abnormal cholangiocyte primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20093497
1558339	Erbin	Erbb2 interacting protein	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19458253
1558339	Erbin	Erbb2 interacting protein	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19458253
1558339	Erbin	Erbb2 interacting protein	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19458253
1558339	Erbin	Erbb2 interacting protein	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20141003	MGI			PMID:19458253
1558339	Erbin	Erbb2 interacting protein	gene	MP:0008814	decreased nerve conduction velocity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19458253
1558341	Gata5	GATA binding protein 5	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20240118	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0000516	abnormal renal/urinary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0001119	abnormal female reproductive system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0001139	abnormal vagina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0001140	abnormal vagina epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0001142	abnormal vagina orifice morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0001613	abnormal vasodilation		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0001859	kidney inflammation		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0002128	abnormal blood circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0003315	abnormal perineum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0003316	perineal fistula		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0003529	enlarged clitoris		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0003541	vaginal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0003550	short perineum		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0003550	short perineum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0003915	increased heart left ventricle weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0004057	thin myocardium compact layer		IAGP		N	RGD:5509061	20240118	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0004067	abnormal trabecula carnea morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0004567	decreased myocardial fiber number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0005528	decreased renal glomerular filtration rate		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0005583	decreased renin activity		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0005600	increased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0008727	increased heart right atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0010408	sinus venosus atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0010419	inlet ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0010428	abnormal heart right ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0010429	abnormal heart left ventricle outflow tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0010463	aorta stenosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0010484	bicuspid aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0010503	myocardial trabeculae hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0010556	thin ventricle myocardium compact layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0010587	conotruncal ridge hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0010595	abnormal aortic valve cusp morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0010640	ventricular myocardium compact layer hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20240118	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0011485	abnormal urethra urothelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0011572	abnormal aorta bulb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21633169
1558341	Gata5	GATA binding protein 5	gene	MP:0011673	unbalanced complete common atrioventricular canal		IAGP		N	RGD:5509061	20210708	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0011749	perivascular fibrosis		IAGP		N	RGD:5509061	20160225	MGI			PMID:26617239
1558341	Gata5	GATA binding protein 5	gene	MP:0011763	urethritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0011780	abnormal female urethra morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0011850	absent clitoral bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0013313	female preputial gland hypoplasia		IAGP		N	RGD:5509061	20141204	MGI			PMID:10866681
1558341	Gata5	GATA binding protein 5	gene	MP:0030992	atrioventricular cushion hypoplasia		IAGP		N	RGD:5509061	20191128	MGI			PMID:19889636
1558341	Gata5	GATA binding protein 5	gene	MP:0031611	decreased fetal cardiomyocyte number		IAGP		N	RGD:5509061	20240321	MGI			PMID:21633169
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20201231	MGI			
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20201022	MGI			
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22966205
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0013292	embryonic lethality prior to organogenesis		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20171012	MGI			PMID:22966205
1558342	Sfpq	splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated)	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20191003	MGI			PMID:29719248
1558343	Snx29	sorting nexin 29	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201231	MGI			
1558343	Snx29	sorting nexin 29	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20211021	MGI			
1558343	Snx29	sorting nexin 29	gene	MP:0011940	decreased food intake		IEA		N	RGD:5509061	20211021	MGI			
1558344	Serf1	small EDRK-rich factor 1	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1558344	Serf1	small EDRK-rich factor 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20160804	MGI			
1558344	Serf1	small EDRK-rich factor 1	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20160804	MGI			
1558344	Serf1	small EDRK-rich factor 1	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20141003	MGI			
1558344	Serf1	small EDRK-rich factor 1	gene	MP:0008079	decreased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20160804	MGI			
1558346	Setmar	SET domain without mariner transposase fusion	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20141003	MGI			
1558346	Setmar	SET domain without mariner transposase fusion	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20160804	MGI			
1558346	Setmar	SET domain without mariner transposase fusion	gene	MP:0003442	decreased circulating glycerol level		IEA		N	RGD:5509061	20141003	MGI			
1558346	Setmar	SET domain without mariner transposase fusion	gene	MP:0009141	increased prepulse inhibition		IEA		N	RGD:5509061	20141003	MGI			
1558348	Vstm5	V-set and transmembrane domain containing 5	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20240523	MGI			
1558348	Vstm5	V-set and transmembrane domain containing 5	gene	MP:0008688	decreased interleukin-2 secretion		IAGP		N	RGD:5509061	20191107	MGI			PMID:30194420
1558349	Lefty1	left right determination factor 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0000542	left-sided isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
1558349	Lefty1	left right determination factor 1	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0002230	abnormal primitive streak formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0002231	abnormal primitive streak morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0002264	abnormal bronchus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0002725	abnormal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0003890	abnormal embryonic-extraembryonic boundary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1558349	Lefty1	left right determination factor 1	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0006065	abnormal heart position or orientation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0006123	tricuspid valve atresia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0006386	absent somites		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0008029	abnormal paraxial mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0008461	left atrial isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1558349	Lefty1	left right determination factor 1	gene	MP:0010117	abnormal lateral plate mesoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0010413	complete atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0010425	abnormal heart and great vessel attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0010668	abnormal hepatic portal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558349	Lefty1	left right determination factor 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0011199	abnormal amniotic cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558349	Lefty1	left right determination factor 1	gene	MP:0011255	abnormal anterior visceral endoderm cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21364967
1558349	Lefty1	left right determination factor 1	gene	MP:0011327	abnormal left renal vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0011569	abnormal azygos vein morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9708731
1558349	Lefty1	left right determination factor 1	gene	MP:0012135	embryonic-extraembryonic boundary constriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:12431380
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000708	thymus hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000714	increased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0002590	increased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0005091	increased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0005561	increased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0006387	abnormal T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0009338	increased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0009341	decreased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0009542	decreased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17442931
1558350	Klf13	Kruppel-like transcription factor 13	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:18285334
1558351	Rnf144a	ring finger protein 144A	gene	MP:0000470	abnormal stomach morphology		IEA		N	RGD:5509061	20181227	MGI			
1558351	Rnf144a	ring finger protein 144A	gene	MP:0002419	abnormal innate immunity		IAGP		N	RGD:5509061	20240502	MGI			PMID:37955227
1558351	Rnf144a	ring finger protein 144A	gene	MP:0020916	increased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20240502	MGI			PMID:37955227
1558351	Rnf144a	ring finger protein 144A	gene	MP:0031026	increased susceptibility to Herpesvirales infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240502	MGI			PMID:37955227
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20230720	MGI			
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802641
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0000496	abnormal small intestine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802641
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20241121	MGI			
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210520	MGI			
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0002816	colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802641
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802641
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802641
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802641
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0009146	abnormal pancreatic acinar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802641
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802641
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:22802641
1558354	Yipf6	Yip1 domain family, member 6	gene	MP:0013486	decreased Paneth cell number		IAGP		N	RGD:5509061	20150611	MGI			PMID:22802641
1558355	Scgb3a2	secretoglobin, family 3A, member 2	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20180920	MGI			PMID:25242865
1558355	Scgb3a2	secretoglobin, family 3A, member 2	gene	MP:0005388	respiratory system phenotype		IAGP		N	RGD:5509061	20210204	MGI			PMID:30768367
1558355	Scgb3a2	secretoglobin, family 3A, member 2	gene	MP:0011053	decreased respiratory motile cilia number		IAGP		N	RGD:5509061	20210204	MGI			PMID:30768367
1558356	Ncapd3	non-SMC condensin II complex, subunit D3	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1558356	Ncapd3	non-SMC condensin II complex, subunit D3	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1558356	Ncapd3	non-SMC condensin II complex, subunit D3	gene	MP:0005178	increased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1558356	Ncapd3	non-SMC condensin II complex, subunit D3	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20220811	MGI			
1558356	Ncapd3	non-SMC condensin II complex, subunit D3	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IEA		N	RGD:5509061	20241017	MGI			
1558356	Ncapd3	non-SMC condensin II complex, subunit D3	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1558358	Cd300c	CD300C molecule	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1558358	Cd300c	CD300C molecule	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20181227	MGI			
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0000250	abnormal vasoconstriction		IAGP		N	RGD:5509061	20141003	MGI			PMID:15860530
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20171012	MGI			PMID:25288642
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15860530
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0001541	abnormal osteoclast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20634945
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0003731	abnormal retina outer nuclear layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0004184	abnormal baroreceptor physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15860530
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0004989	decreased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20634945
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:16143109
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0006243	impaired pupillary reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522242
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0008454	absent retina rod cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0008585	absent photoreceptor outer segment		IAGP		N	RGD:5509061	20141003	MGI			PMID:11114194
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20042581
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0008853	decreased abdominal adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20634945
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0011020	abnormal circadian temperature homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0011021	abnormal circadian regulation of heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17964540
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0011021	abnormal circadian regulation of heart rate		IAGP		N	RGD:5509061	20171012	MGI			PMID:15860530
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0011022	abnormal circadian regulation of systemic arterial blood pressure		IAGP		N	RGD:5509061	20171012	MGI			PMID:15860530
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:20634945
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:10217146
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020467	abnormal circadian behavior		IAGP		N	RGD:5509061	20171012	MGI			PMID:15860530
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020468	abnormal circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:10217146
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:10217146
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:10518585
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:23471982
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:25288642
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:9822380
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020471	abnormal circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:10518585
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:10217146
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020472	arrhythmic circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:10518585
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020473	abnormal circadian behavior phase		IAGP		N	RGD:5509061	20171012	MGI			PMID:11114194
1558359	Cry2	cryptochrome circadian regulator 2	gene	MP:0020477	abnormal locomotor circadian rhythm		IAGP		N	RGD:5509061	20171012	MGI			PMID:11114194
1558360	Irag2	inositol 1,4,5-triphosphate receptor associated 2	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20230601	MGI			
1558361	Spin4	spindlin family, member 4	gene	MP:0001257	increased body length		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0001264	increased body size		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0002176	increased brain weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0004357	long tibia		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0011692	increased chondrocyte number		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558361	Spin4	spindlin family, member 4	gene	MP:0014100	increased chondrocyte proliferation		IAGP		N	RGD:5509061	20240509	MGI			PMID:36927955
1558362	Aph1b	aph1 homolog B, gamma secretase subunit	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:15665098
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530040
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20210128	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220811	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20210128	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0002959	increased urine microalbumin level		IEA		N	RGD:5509061	20210520	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20220811	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19136662
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0005278	abnormal cholesterol homeostasis		IEA		N	RGD:5509061	20211021	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0005464	abnormal platelet physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18524992
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20210128	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20220519	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0008087	decreased T helper 1 cell number		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16530040
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0010220	decreased T-helper 17 cell number		IAGP		N	RGD:5509061	20200130	MGI			PMID:30662948
1558365	Vsig4	V-set and immunoglobulin domain containing 4	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20201231	MGI			
1558366	Lama4	laminin, alpha 4	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0000611	jaundice		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1558366	Lama4	laminin, alpha 4	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814800
1558366	Lama4	laminin, alpha 4	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1558366	Lama4	laminin, alpha 4	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1558366	Lama4	laminin, alpha 4	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814800
1558366	Lama4	laminin, alpha 4	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1558366	Lama4	laminin, alpha 4	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1558366	Lama4	laminin, alpha 4	gene	MP:0001107	decreased Schwann cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1558366	Lama4	laminin, alpha 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1558366	Lama4	laminin, alpha 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1558366	Lama4	laminin, alpha 4	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201231	MGI			
1558366	Lama4	laminin, alpha 4	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814800
1558366	Lama4	laminin, alpha 4	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1558366	Lama4	laminin, alpha 4	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814800
1558366	Lama4	laminin, alpha 4	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0001569	abnormal circulating bilirubin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0001634	internal hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814800
1558366	Lama4	laminin, alpha 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1558366	Lama4	laminin, alpha 4	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1558366	Lama4	laminin, alpha 4	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20201022	MGI			
1558366	Lama4	laminin, alpha 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18794334
1558366	Lama4	laminin, alpha 4	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1558366	Lama4	laminin, alpha 4	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0002651	abnormal sciatic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814800
1558366	Lama4	laminin, alpha 4	gene	MP:0002753	dilated heart left ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20181227	MGI			
1558366	Lama4	laminin, alpha 4	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1558366	Lama4	laminin, alpha 4	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0003658	abnormal capillary morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0003871	abnormal myelin sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814800
1558366	Lama4	laminin, alpha 4	gene	MP:0003993	abnormal ventral spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814800
1558366	Lama4	laminin, alpha 4	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15814800
1558366	Lama4	laminin, alpha 4	gene	MP:0004120	cardiac ischemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0004122	abnormal sinus arrhythmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0004273	abnormal basal lamina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1558366	Lama4	laminin, alpha 4	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17344408
1558366	Lama4	laminin, alpha 4	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0005039	hypoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0005202	lethargy		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0005608	cardiac interstitial fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15699217
1558366	Lama4	laminin, alpha 4	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1558366	Lama4	laminin, alpha 4	gene	MP:0020326	dilated capillary		IAGP		N	RGD:5509061	20160714	MGI			PMID:11809810
1558366	Lama4	laminin, alpha 4	gene	MP:0020326	dilated capillary		IAGP		N	RGD:5509061	20160714	MGI			PMID:16204254
1558366	Lama4	laminin, alpha 4	gene	MP:0020452	abnormal axon radial sorting		IAGP		N	RGD:5509061	20170914	MGI			PMID:15699217
1558366	Lama4	laminin, alpha 4	gene	MP:0020452	abnormal axon radial sorting		IAGP		N	RGD:5509061	20170914	MGI			PMID:15814800
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20240523	MGI			
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201022	MGI			
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20260402	MGI			
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0003131	increased erythrocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20210128	MGI			
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20160421	MGI			
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1558367	Rab5a	RAB5A, member RAS oncogene family	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
1558368	Eefsec	eukaryotic elongation factor, selenocysteine-tRNA-specific	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20240523	MGI			
1558368	Eefsec	eukaryotic elongation factor, selenocysteine-tRNA-specific	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20240523	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20160421	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210128	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20160421	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0000223	decreased monocyte cell number		IEA		N	RGD:5509061	20231207	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0001943	abnormal respiration		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922714
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0002133	abnormal respiratory system physiology		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922714
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0002275	abnormal type II pneumocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20160421	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20160421	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0003982	increased cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20240704	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0004778	increased macrophage derived foam cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0004781	abnormal surfactant composition		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0004782	abnormal surfactant physiology		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20201022	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20160421	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922714
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0005426	tachypnea		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20151112	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160421	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0005630	increased lung weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922714
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922714
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0008245	abnormal alveolar macrophage morphology		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0010810	increased type II pneumocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922714
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0010891	increased alveolar lamellar body number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0010992	increased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0010992	increased surfactant secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23922714
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0010992	increased surfactant secretion		IAGP		N	RGD:5509061	20151210	MGI			PMID:23590306
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0010998	pulmonary alveolar proteinosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23684610
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20250508	MGI			
1558369	Adgrf5	adhesion G protein-coupled receptor F5	gene	MP:0031632	increased lung cholesterol level		IAGP		N	RGD:5509061	20240704	MGI			PMID:23684610
1558370	Flna	filamin, alpha	gene	MP:0000157	abnormal sternum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0000159	abnormal xiphoid process morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0000297	abnormal atrioventricular cushion morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0000364	abnormal vascular regression		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0001319	irregularly shaped pupil		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0001654	hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0001785	edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0001958	emphysema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1558370	Flna	filamin, alpha	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1558370	Flna	filamin, alpha	gene	MP:0002546	mydriasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1558370	Flna	filamin, alpha	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0002633	persistent truncus arteriosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0004003	abnormal vascular endothelial cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0005048	abnormal thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0006055	abnormal vascular endothelial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0006126	abnormal cardiac outflow tract development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0009886	failure of palatal shelf elevation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0009887	abnormal palatal shelf fusion at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0010404	ostium primum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0010620	thick mitral valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11929848
1558370	Flna	filamin, alpha	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16825286
1558370	Flna	filamin, alpha	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558370	Flna	filamin, alpha	gene	MP:0012253	abnormal intersomitic vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17172441
1558372	Cd300a	CD300A molecule	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826299
1558372	Cd300a	CD300A molecule	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210128	MGI			
1558372	Cd300a	CD300A molecule	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
1558372	Cd300a	CD300A molecule	gene	MP:0002423	abnormal mast cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826299
1558372	Cd300a	CD300A molecule	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1558372	Cd300a	CD300A molecule	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20210128	MGI			
1558372	Cd300a	CD300A molecule	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826299
1558372	Cd300a	CD300A molecule	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826299
1558372	Cd300a	CD300A molecule	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826299
1558372	Cd300a	CD300A molecule	gene	MP:0008672	increased interleukin-13 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826299
1558372	Cd300a	CD300A molecule	gene	MP:0008722	abnormal chemokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826299
1558372	Cd300a	CD300A molecule	gene	MP:0009764	decreased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826299
1558372	Cd300a	CD300A molecule	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1558373	Cfap68	cilia and flagella associated protein 68	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20240627	MGI			PMID:38835510
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20200310	MGI			PMID:27840305
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:27840305
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20200310	MGI			PMID:24896341
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:27840305
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0005439	decreased glycogen level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:27840305
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20200310	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:28508477
1558375	Creg1	cellular repressor of E1A-stimulated genes 1	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:27840305
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0001685	abnormal endoderm development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0002085	abnormal embryonic tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0003044	impaired basement membrane formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350012
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:21673655
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0004187	cardia bifida		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0004272	abnormal basement membrane morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0008533	abnormal anterior visceral endoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21350012
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0012157	rostral body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0013283	failure of ventral body wall closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18448090
1558376	Flrt3	fibronectin leucine rich transmembrane protein 3	gene	MP:0013283	failure of ventral body wall closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19056886
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:11113183
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765942
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11113183
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:11113183
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:23742761
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765942
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765942
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0002051	increased skin papilloma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21119595
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0002062	abnormal associative learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23742761
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:11113183
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765942
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24416220
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:23742761
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24416220
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23742761
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21119595
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0003723	abnormal long bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0003932	abnormal molar crown morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24416220
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0004016	decreased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0004033	supernumerary teeth		IAGP		N	RGD:5509061	20141003	MGI			PMID:24416220
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0004377	small frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:24416220
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0004384	small interparietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0004418	small parietal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0005006	abnormal osteoblast physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765942
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765942
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765942
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12765942
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23742761
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23742761
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0010399	decreased skeletal muscle glycogen level		IAGP		N	RGD:5509061	20191226	MGI			PMID:11113183
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0011003	reduced AMPA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23742761
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0011165	abnormal tooth root development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24416220
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0011274	short excitatory postsynaptic current decay time		IAGP		N	RGD:5509061	20141003	MGI			PMID:23742761
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0011862	decreased cranium length		IAGP		N	RGD:5509061	20141003	MGI			PMID:24416220
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0020551	abnormal postsynaptic density morphology		IAGP		N	RGD:5509061	20180301	MGI			PMID:23742761
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0030388	large fontanelles		IAGP		N	RGD:5509061	20171207	MGI			PMID:15109498
1558377	Rps6ka3	ribosomal protein S6 kinase A3	gene	MP:0030536	abnormal diastema morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:24416220
1558378	St6galnac1	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	gene	MP:0000489	abnormal large intestine morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:35303419
1558378	St6galnac1	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20230622	MGI			PMID:35303419
1558378	St6galnac1	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20230622	MGI			PMID:35303419
1558378	St6galnac1	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	gene	MP:0014030	abnormal mucous gland physiology		IAGP		N	RGD:5509061	20230622	MGI			PMID:35303419
1558378	St6galnac1	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	gene	MP:0014219	decreased intestinal mucosa thickness		IAGP		N	RGD:5509061	20230622	MGI			PMID:35303419
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20181220	MGI			PMID:22527485
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000088	short mandible		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000126	brittle teeth		IAGP		N	RGD:5509061	20181220	MGI			PMID:22527485
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:22527485
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000194	increased circulating calcium level		IAGP		N	RGD:5509061	20181220	MGI			PMID:22527485
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000428	abnormal craniofacial morphology		IEA		N	RGD:5509061	20181227	MGI			
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:22527485
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000458	abnormal mandible morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20190502	MGI			
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0002081	perinatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0002639	micrognathia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0002689	abnormal molar morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0002820	abnormal premaxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20181220	MGI			PMID:22527485
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0003056	abnormal hyoid bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0003755	abnormal palate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0004726	abnormal nasal capsule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0004791	absent lower incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0004871	premaxilla hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0005170	cleft upper lip		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0005272	abnormal temporal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0005358	abnormal incisor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0006337	abnormal first pharyngeal arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0008271	abnormal bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0008862	asymmetric snout		IAGP		N	RGD:5509061	20171019	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0009524	absent submandibular gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0009880	decreased mouth size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0009907	decreased tongue size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0009914	abnormal hyoid bone lesser horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0009917	abnormal hyoid bone body morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0010869	decreased bone trabecula number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0010876	decreased bone volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16960803
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0011711	impaired osteoblast differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0014322	short hindlimb		IAGP		N	RGD:5509061	20231130	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0020040	decreased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0020301	short tongue		IAGP		N	RGD:5509061	20221027	MGI			PMID:16751105
1558379	Satb2	special AT-rich sequence binding protein 2	gene	MP:0030868	absent thyroid cartilage		IAGP		N	RGD:5509061	20181101	MGI			PMID:16751105
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0000455	abnormal maxilla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0004235	abnormal masseter muscle morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0009888	palatal shelves fail to meet at midline		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20181227	MGI			
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0012091	increased midbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0012263	decreased hindbrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20201231	MGI			
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0030095	abnormal midface morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:23935987
1558380	Pak1ip1	PAK1 interacting protein 1	gene	MP:0030197	small nasal septum		IAGP		N	RGD:5509061	20171012	MGI			PMID:23935987
1558381	Znhit3	zinc finger, HIT type 3	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20260514	MGI			PMID:40178020
1558381	Znhit3	zinc finger, HIT type 3	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20260514	MGI			PMID:40178020
1558381	Znhit3	zinc finger, HIT type 3	gene	MP:0002663	absent blastocoele		IAGP		N	RGD:5509061	20260514	MGI			PMID:40178020
1558381	Znhit3	zinc finger, HIT type 3	gene	MP:0009781	abnormal preimplantation embryo development		IAGP		N	RGD:5509061	20260514	MGI			PMID:40178020
1558381	Znhit3	zinc finger, HIT type 3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260514	MGI			PMID:40178020
1558381	Znhit3	zinc finger, HIT type 3	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20260514	MGI			PMID:40178020
1558381	Znhit3	zinc finger, HIT type 3	gene	MP:0013272	abnormal translation		IAGP		N	RGD:5509061	20260514	MGI			PMID:40178020
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7845467
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000420	ruffled hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000589	thin tail		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001224	abnormal keratinocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001240	abnormal epidermis stratum corneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001245	thick dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001246	mixed cellular infiltration to dermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001511	disheveled coat		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001577	anemia		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001786	skin edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001835	abnormal antigen presentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7845467
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:7845467
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001868	ovary inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001873	stomach inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0001921	reduced fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002138	abnormal hepatobiliary system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002421	abnormal cell-mediated immunity		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002467	impaired neutrophil phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002490	abnormal immunoglobulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0002928	abnormal bile duct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0003046	liver cirrhosis		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0003325	decreased liver function		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0003326	liver failure		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0003596	epididymis inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0003711	pathological neovascularization		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0004510	myositis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005011	increased eosinophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005078	abnormal cytotoxic T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005095	decreased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005150	cachexia		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005232	abnormal mesenteric lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005416	abnormal circulating protein level		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7845467
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0005616	decreased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0006050	pulmonary fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008024	absent lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14499111
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008343	abnormal gamma-delta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008479	decreased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12810685
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008682	decreased interleukin-17 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21419662
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008752	abnormal tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:9164938
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0010861	increased respiratory mucosa goblet cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:10940923
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0010909	pulmonary alveolar hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0011083	lethality at weaning, complete penetrance		IEA		N	RGD:5509061	20111116	MGI			
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0013587	absent thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:1443055
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0013587	absent thymus medulla		IAGP		N	RGD:5509061	20150319	MGI			PMID:7845467
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:7834753
1558382	Relb	Relb proto-oncogene, NFKB subunit	gene	MP:0020913	increased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:9164938
1558384	Ergic1	endoplasmic reticulum-golgi intermediate compartment 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20211021	MGI			
1558384	Ergic1	endoplasmic reticulum-golgi intermediate compartment 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1558385	Lrch2	leucine-rich repeats and calponin homology (CH) domain containing 2	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20260402	MGI			
1558385	Lrch2	leucine-rich repeats and calponin homology (CH) domain containing 2	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210128	MGI			
1558385	Lrch2	leucine-rich repeats and calponin homology (CH) domain containing 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20241121	MGI			
1558385	Lrch2	leucine-rich repeats and calponin homology (CH) domain containing 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1558385	Lrch2	leucine-rich repeats and calponin homology (CH) domain containing 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20111116	MGI			
1558388	E4f1	E4F transcription factor 1	gene	MP:0000378	absent hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0001191	abnormal skin condition		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0001222	epidermal hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0001234	absent suprabasal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226446
1558388	E4f1	E4F transcription factor 1	gene	MP:0001674	abnormal germ layer development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226446
1558388	E4f1	E4F transcription factor 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226446
1558388	E4f1	E4F transcription factor 1	gene	MP:0001792	impaired wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226446
1558388	E4f1	E4F transcription factor 1	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0009560	absent epidermis stratum granulosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0009759	abnormal hair follicle bulge morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21088222
1558388	E4f1	E4F transcription factor 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15226446
1558389	Epha4	Eph receptor A4	gene	MP:0000860	abnormal primary somatosensory cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035292
1558389	Epha4	Eph receptor A4	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
1558389	Epha4	Eph receptor A4	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20141003	MGI			PMID:12649481
1558389	Epha4	Eph receptor A4	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:24623763
1558389	Epha4	Eph receptor A4	gene	MP:0001052	abnormal innervation pattern to muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600854
1558389	Epha4	Eph receptor A4	gene	MP:0001070	abnormal abducens nerve morphology		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
1558389	Epha4	Eph receptor A4	gene	MP:0001386	abnormal maternal nurturing		IEA		N	RGD:5509061	20111116	MGI			
1558389	Epha4	Eph receptor A4	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20111215	MGI			
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182082
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242070
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:12649481
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:14699416
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102535
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734893
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:20014422
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789074
1558389	Epha4	Eph receptor A4	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20150219	MGI			PMID:24623763
1558389	Epha4	Eph receptor A4	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14699416
1558389	Epha4	Eph receptor A4	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20111116	MGI			
1558389	Epha4	Eph receptor A4	gene	MP:0001524	impaired limb coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789074
1558389	Epha4	Eph receptor A4	gene	MP:0001526	abnormal placing response		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789074
1558389	Epha4	Eph receptor A4	gene	MP:0001922	reduced male fertility		IEA		N	RGD:5509061	20111116	MGI			
1558389	Epha4	Eph receptor A4	gene	MP:0001935	decreased litter size		IEA		N	RGD:5509061	20111116	MGI			
1558389	Epha4	Eph receptor A4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182082
1558389	Epha4	Eph receptor A4	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20014422
1558389	Epha4	Eph receptor A4	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035292
1558389	Epha4	Eph receptor A4	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789074
1558389	Epha4	Eph receptor A4	gene	MP:0002184	abnormal innervation		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
1558389	Epha4	Eph receptor A4	gene	MP:0002286	cryptorchism		IEA		N	RGD:5509061	20111116	MGI			
1558389	Epha4	Eph receptor A4	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182082
1558389	Epha4	Eph receptor A4	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242070
1558389	Epha4	Eph receptor A4	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12649481
1558389	Epha4	Eph receptor A4	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14699416
1558389	Epha4	Eph receptor A4	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789074
1558389	Epha4	Eph receptor A4	gene	MP:0002878	abnormal corticospinal tract morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:24623763
1558389	Epha4	Eph receptor A4	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242070
1558389	Epha4	Eph receptor A4	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11431694
1558389	Epha4	Eph receptor A4	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16600854
1558389	Epha4	Eph receptor A4	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20190815	MGI			PMID:27373307
1558389	Epha4	Eph receptor A4	gene	MP:0003313	abnormal locomotor activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789074
1558389	Epha4	Eph receptor A4	gene	MP:0003477	abnormal nerve fiber response		IAGP		N	RGD:5509061	20150219	MGI			PMID:24623763
1558389	Epha4	Eph receptor A4	gene	MP:0003880	abnormal central pattern generator function		IAGP		N	RGD:5509061	20141003	MGI			PMID:12649481
1558389	Epha4	Eph receptor A4	gene	MP:0003880	abnormal central pattern generator function		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102535
1558389	Epha4	Eph receptor A4	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17035292
1558389	Epha4	Eph receptor A4	gene	MP:0004100	abnormal spinal cord interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1558389	Epha4	Eph receptor A4	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734893
1558389	Epha4	Eph receptor A4	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19182796
1558389	Epha4	Eph receptor A4	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182082
1558389	Epha4	Eph receptor A4	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11242070
1558389	Epha4	Eph receptor A4	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102535
1558389	Epha4	Eph receptor A4	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734893
1558389	Epha4	Eph receptor A4	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789074
1558389	Epha4	Eph receptor A4	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20200507	MGI			PMID:28346224
1558389	Epha4	Eph receptor A4	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102535
1558389	Epha4	Eph receptor A4	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17785183
1558389	Epha4	Eph receptor A4	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19734893
1558389	Epha4	Eph receptor A4	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9789074
1558389	Epha4	Eph receptor A4	gene	MP:0009677	abnormal spinal cord dorsal column morphology		IAGP		N	RGD:5509061	20150219	MGI			PMID:24623763
1558389	Epha4	Eph receptor A4	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20111116	MGI			
1558389	Epha4	Eph receptor A4	gene	MP:0010859	abnormal anterior commissure pars anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182082
1558389	Epha4	Eph receptor A4	gene	MP:0010859	abnormal anterior commissure pars anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102535
1558389	Epha4	Eph receptor A4	gene	MP:0010860	abnormal anterior commissure pars posterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11182082
1558389	Epha4	Eph receptor A4	gene	MP:0010860	abnormal anterior commissure pars posterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16102535
1558389	Epha4	Eph receptor A4	gene	MP:0020529	ectopic thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:16102535
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0002784	abnormal Sertoli cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0005411	delayed fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0008893	detached sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558392	Zpbp2	zona pellucida binding protein 2	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:17664285
1558393	Sp2	Sp2 transcription factor	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141225	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0001700	abnormal embryo turning		IAGP		N	RGD:5509061	20141225	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0011705	absent fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20221402
1558393	Sp2	Sp2 transcription factor	gene	MP:0020083	decreased hippocampus volume		IAGP		N	RGD:5509061	20170706	MGI			PMID:23293287
1558393	Sp2	Sp2 transcription factor	gene	MP:0020394	decreased neuronal precursor proliferation		IAGP		N	RGD:5509061	20170706	MGI			PMID:23293287
1558397	Trappc12	trafficking protein particle complex 12	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20250508	MGI			
1558397	Trappc12	trafficking protein particle complex 12	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1558397	Trappc12	trafficking protein particle complex 12	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20250508	MGI			
1558399	Cbx4	chromobox 4	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362346
1558399	Cbx4	chromobox 4	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1558399	Cbx4	chromobox 4	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201231	MGI			
1558399	Cbx4	chromobox 4	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362346
1558399	Cbx4	chromobox 4	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362346
1558399	Cbx4	chromobox 4	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362346
1558399	Cbx4	chromobox 4	gene	MP:0003763	abnormal thymus physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362346
1558399	Cbx4	chromobox 4	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20160421	MGI			
1558399	Cbx4	chromobox 4	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362346
1558399	Cbx4	chromobox 4	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362346
1558399	Cbx4	chromobox 4	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1558399	Cbx4	chromobox 4	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23362346
1558399	Cbx4	chromobox 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20160421	MGI			
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0000192	abnormal mineral level		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0001303	abnormal lens morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0004624	abnormal thoracic cage morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0005262	coloboma		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0008274	failure of bone ossification		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0009577	abnormal developmental vascular remodeling		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0009653	abnormal palate development		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0010714	iris coloboma		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230119	MGI			
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0013848	subcutaneous edema		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558400	Slc13a4	solute carrier family 13 (sodium/sulfate symporters), member 4	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20170518	MGI			PMID:26292834
1558401	Zfp365	zinc finger protein 365	gene	MP:0000920	abnormal myelination		IAGP		N	RGD:5509061	20141030	MGI			PMID:24481677
1558401	Zfp365	zinc finger protein 365	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23912123
1558401	Zfp365	zinc finger protein 365	gene	MP:0010160	increased oligodendrocyte number		IAGP		N	RGD:5509061	20141030	MGI			PMID:24481677
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16361315
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0003134	increased late pro-B cell number		IAGP		N	RGD:5509061	20240404	MGI			PMID:12055243
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0005022	abnormal immature B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16361315
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16361315
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12055243
1558402	Vpreb1b	V-set pre-B cell surrogate light chain 1B	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:11181696
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20170622	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0000889	abnormal cerebellar molecular layer		IAGP		N	RGD:5509061	20170622	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20170622	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20170622	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20170622	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IEA		N	RGD:5509061	20111116	MGI			
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0008269	abnormal hippocampus CA4 region morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20170622	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0008918	microgliosis		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0012468	decreased striatum size		IAGP		N	RGD:5509061	20181108	MGI			PMID:29349289
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0012779	abnormal brain cholesterol level		IAGP		N	RGD:5509061	20170622	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0014329	abnormal Purkinje cell axon morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:26515654
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0031561	increased ganglioside level		IAGP		N	RGD:5509061	20240704	MGI			PMID:21964919
1558403	Slc9a6	solute carrier family 9 (sodium/hydrogen exchanger), member 6	gene	MP:0031561	increased ganglioside level		IAGP		N	RGD:5509061	20240704	MGI			PMID:26515654
1558404	Zdhhc14	zinc finger, DHHC domain containing 14	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230119	MGI			
1558404	Zdhhc14	zinc finger, DHHC domain containing 14	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230119	MGI			
1558404	Zdhhc14	zinc finger, DHHC domain containing 14	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20230119	MGI			
1558404	Zdhhc14	zinc finger, DHHC domain containing 14	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1558404	Zdhhc14	zinc finger, DHHC domain containing 14	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1558404	Zdhhc14	zinc finger, DHHC domain containing 14	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20230119	MGI			
1558407	Hecw1	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0000745	tremors		IEA		N	RGD:5509061	20181227	MGI			
1558407	Hecw1	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1558407	Hecw1	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20181227	MGI			
1558407	Hecw1	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0001523	impaired righting response		IEA		N	RGD:5509061	20220811	MGI			
1558407	Hecw1	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1558407	Hecw1	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20210506	MGI			PMID:33633267
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20210506	MGI			PMID:33633267
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20160421	MGI			
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0001415	increased exploration in new environment		IEA		N	RGD:5509061	20241121	MGI			
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210506	MGI			PMID:33633267
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33633267
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:33633267
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20210506	MGI			PMID:33633267
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20210506	MGI			PMID:33633267
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20231207	MGI			
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20210506	MGI			PMID:33633267
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20240523	MGI			
1558408	Rimklb	ribosomal modification protein rimK-like family member B	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
1558412	Zfp830	zinc finger protein 830	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191184
1558412	Zfp830	zinc finger protein 830	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210128	MGI			
1558412	Zfp830	zinc finger protein 830	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20210128	MGI			
1558412	Zfp830	zinc finger protein 830	gene	MP:0001728	failure of embryo implantation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15988037
1558412	Zfp830	zinc finger protein 830	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191184
1558412	Zfp830	zinc finger protein 830	gene	MP:0002718	abnormal inner cell mass morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15988037
1558412	Zfp830	zinc finger protein 830	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:15988037
1558412	Zfp830	zinc finger protein 830	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IAGP		N	RGD:5509061	20141003	MGI			PMID:15988037
1558412	Zfp830	zinc finger protein 830	gene	MP:0005028	abnormal trophectoderm morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15988037
1558412	Zfp830	zinc finger protein 830	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191184
1558412	Zfp830	zinc finger protein 830	gene	MP:0011093	embryonic lethality at implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15988037
1558412	Zfp830	zinc finger protein 830	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21191184
1558412	Zfp830	zinc finger protein 830	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558412	Zfp830	zinc finger protein 830	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15988037
1558412	Zfp830	zinc finger protein 830	gene	MP:0012114	absent inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15988037
1558412	Zfp830	zinc finger protein 830	gene	MP:0012118	absent trophectoderm cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15988037
1558412	Zfp830	zinc finger protein 830	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20200402	MGI			
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20190502	MGI			
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001438	aphagia		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20201022	MGI			
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001622	abnormal vasculogenesis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0002641	anisopoikilocytosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0003229	abnormal vitelline vasculature morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0004573	absent limb buds		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0005498	hyporesponsive to tactile stimuli		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0008388	hypochromic microcytic anemia		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0008810	increased circulating iron level		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0009328	delayed heart looping		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0009546	absent gastric milk in neonates		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20220811	MGI			
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0011733	fused somites		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0012132	abnormal midbrain-hindbrain boundary morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0014991	impaired erythrocyte maturation		IAGP		N	RGD:5509061	20260514	MGI			PMID:30692166
1558414	Eps15l1	epidermal growth factor receptor pathway substrate 15-like 1	gene	MP:0030951	abnormal endocytosis		IAGP		N	RGD:5509061	20210318	MGI			PMID:30692166
1558415	Sap30bp	SAP30 binding protein	gene	MP:0001577	anemia		IEA		N	RGD:5509061	20111116	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20201022	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20201022	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0000538	abnormal urinary bladder morphology		IEA		N	RGD:5509061	20201022	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20200514	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20200514	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20200514	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20200514	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20210128	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20200514	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0009552	urinary bladder obstruction		IEA		N	RGD:5509061	20201022	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20200514	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20250508	MGI			
1558416	Naa38	N(alpha)-acetyltransferase 38, NatC auxiliary subunit	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20210826	MGI			
1558417	Poln	DNA polymerase N	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20170713	MGI			PMID:28570559
1558417	Poln	DNA polymerase N	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20170713	MGI			PMID:28570559
1558417	Poln	DNA polymerase N	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170713	MGI			PMID:28570559
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0000562	polydactyly		IEA		N	RGD:5509061	20160804	MGI			
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20220519	MGI			
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20201029	MGI			PMID:31242413
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001260	increased body weight		IEA		N	RGD:5509061	20160804	MGI			
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001556	increased circulating HDL cholesterol level		IEA		N	RGD:5509061	20160804	MGI			
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001756	abnormal urination		IEA		N	RGD:5509061	20160804	MGI			
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201029	MGI			PMID:31242413
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0003179	thrombocytopenia		IEA		N	RGD:5509061	20160804	MGI			
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20201029	MGI			PMID:31242413
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20201029	MGI			PMID:31242413
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20160804	MGI			
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160804	MGI			
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20201029	MGI			PMID:31242413
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0008871	abnormal ovarian follicle number		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20201029	MGI			PMID:31242413
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20201015	MGI			PMID:32345962
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201029	MGI			PMID:31242413
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0011121	decreased primordial ovarian follicle number		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0011125	decreased primary ovarian follicle number		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0011129	decreased tertiary ovarian follicle number		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0014760	impaired DNA repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:32845237
1558419	Hsf2bp	heat shock transcription factor 2 binding protein	gene	MP:0031381	decreased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220616	MGI			PMID:32845237
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0000102	abnormal nasal bone morphology		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0000432	abnormal head morphology		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20211021	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20260402	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0002608	increased hematocrit		IEA		N	RGD:5509061	20220811	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0002699	abnormal vitreous body morphology		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20211021	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0005387	immune system phenotype		IEA		N	RGD:5509061	20260402	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20220811	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0006378	abnormal spermatogonia morphology		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20210826	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0010743	delayed cranial suture closure		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20210114	MGI			PMID:32217665
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20260402	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0013513	decreased memory-marker CD4-negative NK T cell number		IEA		N	RGD:5509061	20260402	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0013772	increased effector memory T-helper cell number		IEA		N	RGD:5509061	20260402	MGI			
1558420	Mettl5	methyltransferase 5, N6-adenosine	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20211021	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20230518	MGI			PMID:35416977
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20241121	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220811	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0000599	enlarged liver		IEA		N	RGD:5509061	20220811	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20230518	MGI			PMID:35416977
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20190502	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20241121	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20260402	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0002619	abnormal lymphocyte morphology		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20210128	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20230518	MGI			PMID:35416977
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0004832	enlarged ovary		IEA		N	RGD:5509061	20220811	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20201022	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0008033	impaired lipolysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0009130	increased white fat cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0009286	increased abdominal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0009476	enlarged cecum		IEA		N	RGD:5509061	20190502	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:23499424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0010124	decreased bone mineral content		IAGP		N	RGD:5509061	20230518	MGI			PMID:35416977
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0010274	increased organ/body region tumor incidence		IAGP		N	RGD:5509061	20231207	MGI			PMID:32619424
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0011964	increased total retina thickness		IEA		N	RGD:5509061	20260402	MGI			
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20230518	MGI			PMID:35416977
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0014143	decreased body fat mass		IAGP		N	RGD:5509061	20230518	MGI			PMID:35416977
1558421	Tbl1xr1	Tbl1x/y related 1	gene	MP:0031415	increased skeletal muscle triglyceride level		IAGP		N	RGD:5509061	20220630	MGI			PMID:23499424
1558423	Dnajb12	DnaJ heat shock protein family (Hsp40) member B12	gene	MP:0000947	convulsive seizures		IEA		N	RGD:5509061	20260402	MGI			
1558423	Dnajb12	DnaJ heat shock protein family (Hsp40) member B12	gene	MP:0000955	abnormal spinal cord morphology		IEA		N	RGD:5509061	20210826	MGI			
1558423	Dnajb12	DnaJ heat shock protein family (Hsp40) member B12	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20211021	MGI			
1558423	Dnajb12	DnaJ heat shock protein family (Hsp40) member B12	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558423	Dnajb12	DnaJ heat shock protein family (Hsp40) member B12	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20160421	MGI			
1558424	Fggy	FGGY carbohydrate kinase domain containing	gene	MP:0004609	vertebral fusion		IEA		N	RGD:5509061	20201231	MGI			
1558425	Tlr13	toll-like receptor 13	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1558425	Tlr13	toll-like receptor 13	gene	MP:0004122	abnormal sinus arrhythmia		IEA		N	RGD:5509061	20260402	MGI			
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20201231	MGI			
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0008544	impaired olfaction		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0009948	abnormal olfactory bulb glomerular layer morphology		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0011677	abnormal olfactory sensory neuron physiology		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0012020	abnormal olfactory epithelium physiology		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558426	Ric8b	RIC8 guanine nucleotide exchange factor B	gene	MP:0020348	decreased olfactory sensory neuron number		IAGP		N	RGD:5509061	20180322	MGI			PMID:29118104
1558427	Taar8b	trace amine-associated receptor 8B	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20210520	MGI			
1558427	Taar8b	trace amine-associated receptor 8B	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20210520	MGI			
1558427	Taar8b	trace amine-associated receptor 8B	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20220811	MGI			
1558427	Taar8b	trace amine-associated receptor 8B	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20221215	MGI			
1558427	Taar8b	trace amine-associated receptor 8B	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20211021	MGI			
1558427	Taar8b	trace amine-associated receptor 8B	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1558427	Taar8b	trace amine-associated receptor 8B	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20221215	MGI			
1558427	Taar8b	trace amine-associated receptor 8B	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20260402	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002018	increased malignant tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002038	increased carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002175	decreased brain weight		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0004207	increased squamous cell carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0009312	increased jejunum adenocarcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210805	MGI			
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0010138	arteritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0010383	increased adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558429	Ssbp2	single-stranded DNA binding protein 2	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20348955
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0000602	dilated liver sinusoidal space		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0003266	biliary cyst		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0008432	abnormal long-term spatial reference memory		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0010420	muscular ventricular septal defect		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0010484	bicuspid aortic valve		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0010602	abnormal pulmonary valve cusp morphology		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0013875	increased trigeminal neuroma incidence		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0013968	multiple persisting craniopharyngeal ducts		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0013973	abnormal hepatic vein connection		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0014001	abnormal vertebral artery topology		IEA		N	RGD:5509061	20170504	MGI			
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0014370	impaired spatial working memory		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0014416	decreased social novelty preference		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0020335	abnormal dentate gyrus neuron dendrite morphology		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0020507	increased dendritic spine density		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0020508	decreased dendritic spine density		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0020510	increased dendritic spine length		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0021018	decreased dendritic spine number		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0021019	increased dendritic spine number		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0021111	decreased social investigation		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558430	Capza2	capping actin protein of muscle Z-line subunit alpha 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20251023	MGI			PMID:40659881
1558431	Rhox13	reproductive homeobox 13	gene	MP:0002161	abnormal fertility/fecundity		IAGP		N	RGD:5509061	20170622	MGI			PMID:27486269
1558431	Rhox13	reproductive homeobox 13	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20170622	MGI			PMID:27486269
1558431	Rhox13	reproductive homeobox 13	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20170622	MGI			PMID:27486269
1558431	Rhox13	reproductive homeobox 13	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20170622	MGI			PMID:27486269
1558431	Rhox13	reproductive homeobox 13	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20170622	MGI			PMID:27486269
1558432	Lysmd1	LysM, putative peptidoglycan-binding, domain containing 1	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20210826	MGI			
1558432	Lysmd1	LysM, putative peptidoglycan-binding, domain containing 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20211021	MGI			
1558433	Sik2	salt inducible kinase 2	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1558433	Sik2	salt inducible kinase 2	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0004890	decreased energy expenditure		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20150129	MGI			PMID:20819186
1558433	Sik2	salt inducible kinase 2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0008034	enhanced lipolysis		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0014172	decreased fatty acid oxidation		IAGP		N	RGD:5509061	20160505	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0030022	decreased muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0030968	decreased circulating adiponectin level		IAGP		N	RGD:5509061	20190815	MGI			PMID:24898145
1558433	Sik2	salt inducible kinase 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:24898145
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000794	abnormal parietal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000798	abnormal frontal lobe morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000832	abnormal thalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0000952	abnormal CNS glial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18324732
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18324732
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:18324732
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977657
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0002199	abnormal brain commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0002316	anoxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0002961	abnormal axon guidance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0003005	abnormal hippocampal fimbria morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18324732
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0004267	abnormal optic tract morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0008219	abnormal dorsal telencephalic commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977657
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0008440	abnormal subplate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0008441	thin cortical plate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0009969	abnormal cerebral cortex pyramidal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0010825	abnormal lung saccule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18324732
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0010859	abnormal anterior commissure pars anterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0010860	abnormal anterior commissure pars posterior morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977657
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977657
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18324732
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17977657
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12897243
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0020546	increased hippocampal fornix size		IAGP		N	RGD:5509061	20180301	MGI			PMID:15572149
1558435	Mapk8ip3	mitogen-activated protein kinase 8 interacting protein 3	gene	MP:0020549	increased optic chiasm size		IAGP		N	RGD:5509061	20180301	MGI			PMID:15572149
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0000542	left-sided isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131974
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131974
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20220811	MGI			
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131974
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131974
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0004131	abnormal motile primary cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131974
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131974
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0010854	lung situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131974
1558436	Ccdc40	coiled-coil domain containing 40	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21131974
1558437	Prss33	serine protease 33	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0001262	decreased body weight		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20220519	MGI			
1558437	Prss33	serine protease 33	gene	MP:0004906	enlarged uterus		IEA		N	RGD:5509061	20220519	MGI			
1558438	Scd4	stearoyl-coenzyme A desaturase 4	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20250213	MGI			PMID:36142371
1558438	Scd4	stearoyl-coenzyme A desaturase 4	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20250213	MGI			PMID:36142371
1558438	Scd4	stearoyl-coenzyme A desaturase 4	gene	MP:0020447	decreased NAD(P)H oxidase activity		IAGP		N	RGD:5509061	20250213	MGI			PMID:36142371
1558440	Prmt8	protein arginine N-methyltransferase 8	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20251204	MGI			PMID:26665171
1558440	Prmt8	protein arginine N-methyltransferase 8	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20161124	MGI			PMID:26665171
1558440	Prmt8	protein arginine N-methyltransferase 8	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20161124	MGI			PMID:26665171
1558440	Prmt8	protein arginine N-methyltransferase 8	gene	MP:0001413	abnormal response to new environment		IAGP		N	RGD:5509061	20161124	MGI			PMID:26665171
1558440	Prmt8	protein arginine N-methyltransferase 8	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20161124	MGI			PMID:26665171
1558440	Prmt8	protein arginine N-methyltransferase 8	gene	MP:0003990	decreased neurotransmitter release		IAGP		N	RGD:5509061	20161124	MGI			PMID:26665171
1558440	Prmt8	protein arginine N-methyltransferase 8	gene	MP:0008572	abnormal Purkinje cell dendrite morphology		IAGP		N	RGD:5509061	20161124	MGI			PMID:26665171
1558441	C1d	C1D nuclear receptor co-repressor	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20230119	MGI			
1558441	C1d	C1D nuclear receptor co-repressor	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1558442	Pgk2	phosphoglycerate kinase 2	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759366
1558442	Pgk2	phosphoglycerate kinase 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759366
1558442	Pgk2	phosphoglycerate kinase 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19759366
1558442	Pgk2	phosphoglycerate kinase 2	gene	MP:0020451	decreased sperm progressive motility		IAGP		N	RGD:5509061	20220303	MGI			PMID:19759366
1558445	Mid2	midline 2	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20181227	MGI			
1558445	Mid2	midline 2	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20181227	MGI			
1558445	Mid2	midline 2	gene	MP:0001192	scaly skin		IEA		N	RGD:5509061	20181227	MGI			
1558445	Mid2	midline 2	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20181227	MGI			
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445275
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445275
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20210311	MGI			PMID:33232677
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20160804	MGI			
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445275
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20210311	MGI			PMID:33232677
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20160804	MGI			
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20160804	MGI			
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20160804	MGI			
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20210311	MGI			PMID:33232677
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0010174	decreased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21445275
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20210311	MGI			PMID:33232677
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210311	MGI			PMID:33232677
1558448	Kdm4b	lysine (K)-specific demethylase 4B	gene	MP:0012460	decreased dentate gyrus size		IAGP		N	RGD:5509061	20210311	MGI			PMID:33232677
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000443	abnormal snout morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000913	abnormal brain development		IEA		N	RGD:5509061	20111116	MGI			
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000919	cranioschisis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:22801502
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001177	atelectasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001722	pale yolk sac		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002188	small heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002417	abnormal megakaryocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002441	abnormal granulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0002925	abnormal cardiovascular development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003139	patent ductus arteriosus		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003232	abnormal forebrain development		IEA		N	RGD:5509061	20111116	MGI			
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003400	kinked neural tube		IEA		N	RGD:5509061	20111116	MGI			
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003677	abnormal ear lobe morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003743	abnormal facial morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003794	delayed somite formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003795	abnormal bone structure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22801502
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0004029	spontaneous chromosome breakage		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0004073	caudal body truncation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0004251	failure of heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0004380	short frontal bone		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0004979	abnormal neuronal precursor cell number		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0005221	abnormal rostral-caudal axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0005287	narrow eye opening		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0005481	increased chronic myelocytic leukemia incidence		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0005587	abnormal Meckel's cartilage morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0006207	embryonic lethality during organogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22801502
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0008534	enlarged fourth ventricle		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0008536	enlarged third ventricle		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0009397	increased trophoblast giant cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0010503	myocardial trabeculae hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0010725	thin interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949634
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23028370
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23365460
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22801502
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22826230
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20260709	MGI			PMID:36412518
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0012185	abnormal muscle precursor cell morphology		IAGP		N	RGD:5509061	20160721	MGI			PMID:26999603
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0012754	abnormal cranial neural crest cell morphology		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0013239	impaired skeletal muscle regeneration		IAGP		N	RGD:5509061	20160721	MGI			PMID:26999603
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0013545	cleft hard palate		IAGP		N	RGD:5509061	20220915	MGI			PMID:32541010
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0013663	increased myeloid cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0013696	increased granulocyte monocyte progenitor cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0013705	decreased megakaryocyte-erythroid progenitor cell number		IAGP		N	RGD:5509061	20180830	MGI			PMID:29479066
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0030031	abnormal forehead morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0030049	prominent forehead		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0030115	abnormal nasal tip morphology		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558450	Kdm6a	lysine (K)-specific demethylase 6A	gene	MP:0030275	thin frontal bone		IAGP		N	RGD:5509061	20260709	MGI			PMID:29073101
1558451	Kcnk7	potassium channel, subfamily K, member 7	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:18572259
1558452	Slc25a23	solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20260402	MGI			
1558452	Slc25a23	solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20260402	MGI			
1558452	Slc25a23	solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23344948
1558452	Slc25a23	solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23	gene	MP:0011467	decreased urine urea nitrogen level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23344948
1558453	Sh2d1b1	SH2 domain containing 1B1	gene	MP:0003080	increased natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127454
1558453	Sh2d1b1	SH2 domain containing 1B1	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151721
1558453	Sh2d1b1	SH2 domain containing 1B1	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962259
1558453	Sh2d1b1	SH2 domain containing 1B1	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16127454
1558453	Sh2d1b1	SH2 domain containing 1B1	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20962259
1558453	Sh2d1b1	SH2 domain containing 1B1	gene	MP:0010766	abnormal NK cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22683124
1558454	Itga4	integrin alpha 4	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645544
1558454	Itga4	integrin alpha 4	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470243
1558454	Itga4	integrin alpha 4	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539359
1558454	Itga4	integrin alpha 4	gene	MP:0001711	abnormal placenta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539359
1558454	Itga4	integrin alpha 4	gene	MP:0001726	abnormal allantois morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539359
1558454	Itga4	integrin alpha 4	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645544
1558454	Itga4	integrin alpha 4	gene	MP:0002127	abnormal cardiovascular system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539359
1558454	Itga4	integrin alpha 4	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645544
1558454	Itga4	integrin alpha 4	gene	MP:0002414	abnormal myeloblast morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645544
1558454	Itga4	integrin alpha 4	gene	MP:0002424	abnormal reticulocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645544
1558454	Itga4	integrin alpha 4	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470243
1558454	Itga4	integrin alpha 4	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470243
1558454	Itga4	integrin alpha 4	gene	MP:0003156	abnormal leukocyte migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18809756
1558454	Itga4	integrin alpha 4	gene	MP:0003628	abnormal leukocyte adhesion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18809756
1558454	Itga4	integrin alpha 4	gene	MP:0003799	impaired macrophage chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470243
1558454	Itga4	integrin alpha 4	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470243
1558454	Itga4	integrin alpha 4	gene	MP:0004557	dilated allantois		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539359
1558454	Itga4	integrin alpha 4	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18809756
1558454	Itga4	integrin alpha 4	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18809756
1558454	Itga4	integrin alpha 4	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18809756
1558454	Itga4	integrin alpha 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18583710
1558454	Itga4	integrin alpha 4	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:14645544
1558454	Itga4	integrin alpha 4	gene	MP:0008133	decreased Peyer's patch number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16470243
1558454	Itga4	integrin alpha 4	gene	MP:0008135	small Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:18809756
1558454	Itga4	integrin alpha 4	gene	MP:0008247	abnormal mononuclear cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18809756
1558454	Itga4	integrin alpha 4	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:12021259
1558454	Itga4	integrin alpha 4	gene	MP:0009657	failure of chorioallantoic fusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539359
1558454	Itga4	integrin alpha 4	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:12021259
1558454	Itga4	integrin alpha 4	gene	MP:0009698	heart hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539359
1558454	Itga4	integrin alpha 4	gene	MP:0009858	abnormal cellular extravasation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18809756
1558454	Itga4	integrin alpha 4	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539359
1558454	Itga4	integrin alpha 4	gene	MP:0010555	absent epicardium		IAGP		N	RGD:5509061	20240229	MGI			PMID:12021259
1558454	Itga4	integrin alpha 4	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12021259
1558454	Itga4	integrin alpha 4	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7539359
1558454	Itga4	integrin alpha 4	gene	MP:0031590	abnormal epicardium development		IAGP		N	RGD:5509061	20240229	MGI			PMID:12021259
1558454	Itga4	integrin alpha 4	gene	MP:0031590	abnormal epicardium development		IAGP		N	RGD:5509061	20240229	MGI			PMID:7539359
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0001554	increased circulating free fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0003949	abnormal circulating lipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0003961	decreased lean body mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0004777	abnormal phospholipid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0009285	increased gonadal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0009292	increased inguinal fat pad weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0014814	increased brain glucose metabolism		IAGP		N	RGD:5509061	20251204	MGI			PMID:23459938
1558456	Acot7	acyl-CoA thioesterase 7	gene	MP:0020523	decreased susceptibility to induced hypothermia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23459938
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0001648	abnormal apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:14961764
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0002717	abnormal male preputial gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:14961764
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0002717	abnormal male preputial gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0005166	decreased susceptibility to injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0008114	abnormal Kupffer cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19637241
1558458	Uaca	uveal autoantigen with coiled-coil domains and ankyrin repeats	gene	MP:0011971	increased circulating lactate dehydrogenase level		IAGP		N	RGD:5509061	20210218	MGI			PMID:19637241
1558459	Ubn2	ubinuclein 2	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20221215	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20210826	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20211021	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210826	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1558459	Ubn2	ubinuclein 2	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20210826	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1558459	Ubn2	ubinuclein 2	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20230601	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20210826	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1558459	Ubn2	ubinuclein 2	gene	MP:0004180	failure of initiation of embryo turning		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1558459	Ubn2	ubinuclein 2	gene	MP:0005562	decreased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0009263	abnormal eyelid fusion		IEA		N	RGD:5509061	20221215	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0009908	protruding tongue		IEA		N	RGD:5509061	20221215	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1558459	Ubn2	ubinuclein 2	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1558459	Ubn2	ubinuclein 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20260528	MGI			PMID:40455860
1558459	Ubn2	ubinuclein 2	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20210826	MGI			
1558459	Ubn2	ubinuclein 2	gene	MP:0011496	abnormal head size		IEA		N	RGD:5509061	20210826	MGI			
1558462	Lax1	lymphocyte transmembrane adaptor 1	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843560
1558462	Lax1	lymphocyte transmembrane adaptor 1	gene	MP:0002359	abnormal spleen germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843560
1558462	Lax1	lymphocyte transmembrane adaptor 1	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843560
1558462	Lax1	lymphocyte transmembrane adaptor 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843560
1558462	Lax1	lymphocyte transmembrane adaptor 1	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843560
1558462	Lax1	lymphocyte transmembrane adaptor 1	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843560
1558462	Lax1	lymphocyte transmembrane adaptor 1	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843560
1558462	Lax1	lymphocyte transmembrane adaptor 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:15843560
1558462	Lax1	lymphocyte transmembrane adaptor 1	gene	MP:0014469	abnormal B cell calcium ion homeostasis		IAGP		N	RGD:5509061	20240613	MGI			PMID:15843560
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000019	thick ears		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000136	abnormal microglial cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000137	abnormal vertebrae morphology		IEA		N	RGD:5509061	20181227	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122996
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000316	cellular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000316	cellular necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122996
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:1686018
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000572	abnormal autopod morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000573	increased hindlimb autopod size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000580	deformed nails		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122996
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122996
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:1686018
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20181227	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122996
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20181227	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001192	scaly skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001209	spontaneous skin ulceration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20210128	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001442	decreased grooming behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122996
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001849	ear inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0001968	abnormal touch/nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20181227	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20181227	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002111	abnormal tail morphology		IEA		N	RGD:5509061	20181227	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002177	abnormal outer ear morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122996
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002339	abnormal lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122996
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002497	increased IgE level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002499	chronic inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:1686018
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002875	decreased erythrocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20181227	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0004947	skin inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0005190	osteomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10678414
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0005190	osteomyelitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16122996
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0008254	increased megakaryocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22646813
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0008500	increased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16397132
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20181227	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1558463	Pstpip2	proline-serine-threonine phosphatase-interacting protein 2	gene	MP:0030422	abnormal outer ear cartilage morphology		IAGP		N	RGD:5509061	20171214	MGI			PMID:16122996
1558464	Tspan33	tetraspanin 33	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0000248	macrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0002447	abnormal erythrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0008019	increased liver tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558464	Tspan33	tetraspanin 33	gene	MP:0010175	leptocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17158226
1558466	Lrrc51	leucine rich repeat containing 51	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1558466	Lrrc51	leucine rich repeat containing 51	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20190502	MGI			
1558466	Lrrc51	leucine rich repeat containing 51	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1558467	Shb	src homology 2 domain-containing transforming protein B	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676633
1558467	Shb	src homology 2 domain-containing transforming protein B	gene	MP:0001672	abnormal embryo development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676633
1558467	Shb	src homology 2 domain-containing transforming protein B	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676633
1558467	Shb	src homology 2 domain-containing transforming protein B	gene	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676633
1558467	Shb	src homology 2 domain-containing transforming protein B	gene	MP:0006281	abnormal tail development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676633
1558467	Shb	src homology 2 domain-containing transforming protein B	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676633
1558467	Shb	src homology 2 domain-containing transforming protein B	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17676633
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20260402	MGI			
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20181227	MGI			
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15263032
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:15263032
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339556
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23840879
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15263032
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339556
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15263032
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339556
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16339556
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210826	MGI			
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0004357	long tibia		IEA		N	RGD:5509061	20250508	MGI			
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:23840879
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15263032
1558468	Marco	macrophage receptor with collagenous structure	gene	MP:0010740	abnormal dendritic cell chemotaxis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23840879
1558470	Osbpl10	oxysterol binding protein-like 10	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1558471	Tceal9	transcription elongation factor A like 9	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1558471	Tceal9	transcription elongation factor A like 9	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20210128	MGI			
1558472	Aimp2	aminoacyl tRNA synthetase complex-interacting multifunctional protein 2	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20260402	MGI			
1558472	Aimp2	aminoacyl tRNA synthetase complex-interacting multifunctional protein 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20260402	MGI			
1558472	Aimp2	aminoacyl tRNA synthetase complex-interacting multifunctional protein 2	gene	MP:0001711	abnormal placenta morphology		IEA		N	RGD:5509061	20260402	MGI			
1558472	Aimp2	aminoacyl tRNA synthetase complex-interacting multifunctional protein 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12060739
1558472	Aimp2	aminoacyl tRNA synthetase complex-interacting multifunctional protein 2	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20260402	MGI			
1558472	Aimp2	aminoacyl tRNA synthetase complex-interacting multifunctional protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20260402	MGI			
1558473	Ddx54	DEAD box helicase 54	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1558473	Ddx54	DEAD box helicase 54	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558473	Ddx54	DEAD box helicase 54	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1558473	Ddx54	DEAD box helicase 54	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1558474	Dip2a	disco interacting protein 2 homolog A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210603	MGI			PMID:33184751
1558474	Dip2a	disco interacting protein 2 homolog A	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210603	MGI			PMID:33184751
1558474	Dip2a	disco interacting protein 2 homolog A	gene	MP:0003053	delayed tooth eruption		IAGP		N	RGD:5509061	20210603	MGI			PMID:33184751
1558474	Dip2a	disco interacting protein 2 homolog A	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20210603	MGI			PMID:33184751
1558474	Dip2a	disco interacting protein 2 homolog A	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20211021	MGI			
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0000519	hydronephrosis		IAGP		N	RGD:5509061	20190530	MGI			PMID:29483821
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0000585	kinked tail		IAGP		N	RGD:5509061	20190530	MGI			PMID:29483821
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0001948	vesicoureteral reflux		IAGP		N	RGD:5509061	20190530	MGI			PMID:29483821
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0002621	delayed neural tube closure		IAGP		N	RGD:5509061	20190530	MGI			PMID:29483821
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0003604	single kidney		IAGP		N	RGD:5509061	20190530	MGI			PMID:29483821
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0004017	duplex kidney		IAGP		N	RGD:5509061	20190530	MGI			PMID:29483821
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20190530	MGI			PMID:29483821
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20230126	MGI			PMID:27383418
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0006032	abnormal ureteric bud morphology		IAGP		N	RGD:5509061	20190530	MGI			PMID:29483821
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0010980	ectopic ureteric bud		IAGP		N	RGD:5509061	20190530	MGI			PMID:29483821
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230126	MGI			PMID:27383418
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20230126	MGI			PMID:27383418
1558475	Gen1	GEN1, Holliday junction 5' flap endonuclease	gene	MP:0014040	increased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20230126	MGI			PMID:27383418
1558476	Endov	endonuclease V	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20240523	MGI			
1558476	Endov	endonuclease V	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20240523	MGI			
1558476	Endov	endonuclease V	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20200910	MGI			PMID:32083667
1558476	Endov	endonuclease V	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20240523	MGI			
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23376831
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20151217	MGI			PMID:26311765
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20151217	MGI			PMID:26311765
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0001876	decreased inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:18542050
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20170323	MGI			
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:21709234
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0002442	abnormal leukocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18542050
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0002446	abnormal macrophage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23596170
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18542050
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23596170
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20240523	MGI			
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0003332	liver abscess		IAGP		N	RGD:5509061	20141003	MGI			PMID:21709234
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23376831
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23376831
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:23376831
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20151217	MGI			PMID:26311765
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23376831
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21709234
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21709234
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0008618	decreased circulating interleukin-12 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21709234
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0008648	decreased circulating interleukin-12b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21709234
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0008664	decreased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21709234
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0008719	impaired neutrophil recruitment		IAGP		N	RGD:5509061	20141003	MGI			PMID:18542050
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18542050
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18542050
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20151217	MGI			PMID:26311765
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21709234
1558477	Trpm2	transient receptor potential cation channel, subfamily M, member 2	gene	MP:0010579	increased heart left ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23376831
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20231207	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20220519	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0000222	decreased neutrophil cell number		IEA		N	RGD:5509061	20260402	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20220811	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0000650	mesocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20231207	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0000747	muscle weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560552
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0001120	abnormal uterus morphology		IEA		N	RGD:5509061	20231207	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560552
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0001274	curly vibrissae		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0001706	abnormal left-right axis patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560552
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20231207	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20231207	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17083490
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002080	prenatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002102	abnormal ear morphology		IEA		N	RGD:5509061	20220811	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560552
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002654	spongiform encephalopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20211021	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220519	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560552
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20201231	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0004158	right aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20201022	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0004952	increased spleen weight		IEA		N	RGD:5509061	20220811	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0005013	increased lymphocyte cell number		IEA		N	RGD:5509061	20221215	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20220519	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220519	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560552
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220519	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0006138	congestive heart failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0008025	brain vacuoles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12560552
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0010334	pleural effusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0010393	shortened QRS complex duration		IEA		N	RGD:5509061	20210128	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0010403	atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0010426	abnormal heart and great artery attachment		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0010436	abnormal coronary sinus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0010488	abnormal left subclavian artery morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0010854	lung situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17075880
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20200402	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20220811	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0011874	enlarged urinary bladder		IEA		N	RGD:5509061	20231207	MGI			
1558478	Mgrn1	mahogunin, ring finger 1	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20241121	MGI			
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0000125	absent incisors		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0000400	abnormal awl hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0000414	alopecia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0002100	abnormal tooth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694322
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0004811	abnormal neuron physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15694322
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0006363	absent auchene hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0006365	absent guard hair		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0006366	absent zigzag hairs		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0006367	absent sweat gland		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0006400	decreased molar number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0013370	anhidrosis		IAGP		N	RGD:5509061	20141225	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0030457	abnormal molar cusp morphology		IAGP		N	RGD:5509061	20180125	MGI			PMID:18689798
1558479	Tnfrsf19	tumor necrosis factor receptor superfamily, member 19	gene	MP:0031384	impaired blood-brain barrier function		IAGP		N	RGD:5509061	20220407	MGI			PMID:22340501
1558480	H3c14	H3 clustered histone 14	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0001312	abnormal cornea morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0001329	retina hyperplasia		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0005545	abnormal lens development		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0006086	decreased body mass index		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0011962	increased cornea thickness		IAGP		N	RGD:5509061	20190815	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0031206	hypolipidemia		IAGP		N	RGD:5509061	20210211	MGI			PMID:30991053
1558480	H3c14	H3 clustered histone 14	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:30991053
1558481	Tsku	tsukushi, small leucine rich proteoglycan	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21055390
1558481	Tsku	tsukushi, small leucine rich proteoglycan	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21055390
1558481	Tsku	tsukushi, small leucine rich proteoglycan	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21055390
1558482	Ranbp2	RAN binding protein 2	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20210128	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20210128	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20210128	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0003331	increased hepatocellular carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0003694	failure of blastocyst to hatch from the zona pellucida		IEA		N	RGD:5509061	20241010	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0003701	elevated level of mitotic sister chromatid exchange		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17069463
1558482	Ranbp2	RAN binding protein 2	gene	MP:0004024	aneuploidy		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0004046	abnormal mitosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20210128	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17069463
1558482	Ranbp2	RAN binding protein 2	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17069463
1558482	Ranbp2	RAN binding protein 2	gene	MP:0008714	increased lung carcinoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17069463
1558482	Ranbp2	RAN binding protein 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18394993
1558482	Ranbp2	RAN binding protein 2	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IEA		N	RGD:5509061	20241010	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0012058	abnormal morula morphology		IEA		N	RGD:5509061	20241010	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0012129	failure of blastocyst formation		IEA		N	RGD:5509061	20241010	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1558482	Ranbp2	RAN binding protein 2	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:17069463
1558483	Patj	PATJ, crumbs cell polarity complex component	gene	MP:0001486	abnormal startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1558483	Patj	PATJ, crumbs cell polarity complex component	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20230601	MGI			
1558484	Slamf7	SLAM family member 7	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:19151721
1558487	Pabpc5	poly(A) binding protein, cytoplasmic 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210520	MGI			
1558487	Pabpc5	poly(A) binding protein, cytoplasmic 5	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210520	MGI			
1558491	Zfp329	zinc finger protein 329	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20201231	MGI			
1558491	Zfp329	zinc finger protein 329	gene	MP:0002546	mydriasis		IEA		N	RGD:5509061	20240523	MGI			
1558491	Zfp329	zinc finger protein 329	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20201231	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20210128	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20220811	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20211021	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160421	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20201224	MGI			PMID:25143383
1558492	Bex2	brain expressed X-linked 2	gene	MP:0002757	decreased vertical activity		IEA		N	RGD:5509061	20260402	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20211021	MGI			
1558492	Bex2	brain expressed X-linked 2	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20250508	MGI			
1558493	Slitrk3	SLIT and NTRK-like family, member 3	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20160804	MGI			PMID:22286174
1558493	Slitrk3	SLIT and NTRK-like family, member 3	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20160804	MGI			PMID:22286174
1558493	Slitrk3	SLIT and NTRK-like family, member 3	gene	MP:0014383	decreased miniature inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20240404	MGI			PMID:22286174
1558493	Slitrk3	SLIT and NTRK-like family, member 3	gene	MP:0015055	decreased synapse density		IAGP		N	RGD:5509061	20260813	MGI			PMID:22286174
1558494	Usp4	ubiquitin specific peptidase 4	gene	MP:0004227	increased cellular sensitivity to ionizing radiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21522127
1558494	Usp4	ubiquitin specific peptidase 4	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20240516	MGI			PMID:30514904
1558494	Usp4	ubiquitin specific peptidase 4	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21522127
1558494	Usp4	ubiquitin specific peptidase 4	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21522127
1558494	Usp4	ubiquitin specific peptidase 4	gene	MP:0008410	increased cellular sensitivity to ultraviolet irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21522127
1558494	Usp4	ubiquitin specific peptidase 4	gene	MP:0009322	increased splenocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21522127
1558494	Usp4	ubiquitin specific peptidase 4	gene	MP:0009541	increased thymocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21522127
1558497	Tlr7	toll-like receptor 7	gene	MP:0000220	increased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606711
1558497	Tlr7	toll-like receptor 7	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1558497	Tlr7	toll-like receptor 7	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0000696	abnormal Peyer's patch morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0000701	abnormal lymph node size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0001844	autoimmune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1558497	Tlr7	toll-like receptor 7	gene	MP:0001846	increased inflammatory response		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0001869	pancreas inflammation		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1558497	Tlr7	toll-like receptor 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0002108	abnormal muscle morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1558497	Tlr7	toll-like receptor 7	gene	MP:0002362	abnormal spleen marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1558497	Tlr7	toll-like receptor 7	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0002723	abnormal immune serum protein physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606711
1558497	Tlr7	toll-like receptor 7	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606711
1558497	Tlr7	toll-like receptor 7	gene	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0002870	decreased anti-insulin autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0003725	increased autoantibody level		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0003726	decreased autoantibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0003865	lymph node inflammation		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1558497	Tlr7	toll-like receptor 7	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1558497	Tlr7	toll-like receptor 7	gene	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0004802	decreased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18606711
1558497	Tlr7	toll-like receptor 7	gene	MP:0004953	decreased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0005220	abnormal exocrine pancreas morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008171	abnormal mature B cell morphology		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1558497	Tlr7	toll-like receptor 7	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0008496	decreased IgG2a level		IAGP		N	RGD:5509061	20141003	MGI			PMID:20811154
1558497	Tlr7	toll-like receptor 7	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008561	decreased tumor necrosis factor secretion		IEA		N	RGD:5509061	20111116	MGI			
1558497	Tlr7	toll-like receptor 7	gene	MP:0008563	decreased interferon-alpha secretion		IAGP		N	RGD:5509061	20200423	MGI			PMID:16985170
1558497	Tlr7	toll-like receptor 7	gene	MP:0008574	decreased circulating interferon-alpha level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15034168
1558497	Tlr7	toll-like receptor 7	gene	MP:0008577	increased circulating interferon-gamma level		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008670	decreased interleukin-12b secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:16461338
1558497	Tlr7	toll-like receptor 7	gene	MP:0008769	abnormal plasmacytoid dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16973389
1558497	Tlr7	toll-like receptor 7	gene	MP:0008769	abnormal plasmacytoid dendritic cell physiology		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0008783	decreased B cell apoptosis		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0009318	increased splenic marginal zone lymphoma incidence		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0009333	abnormal splenocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1558497	Tlr7	toll-like receptor 7	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17997333
1558497	Tlr7	toll-like receptor 7	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0011353	expanded mesangial matrix		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558497	Tlr7	toll-like receptor 7	gene	MP:0020519	renal glomerular immunoglobulin deposits		IAGP		N	RGD:5509061	20220623	MGI			PMID:35477763
1558498	Mbtps2	membrane-bound transcription factor peptidase, site 2	gene	MP:0000130	abnormal trabecular bone morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:37797712
1558498	Mbtps2	membrane-bound transcription factor peptidase, site 2	gene	MP:0006205	embryonic lethality between implantation and somite formation		IAGP		N	RGD:5509061	20240404	MGI			PMID:37797712
1558498	Mbtps2	membrane-bound transcription factor peptidase, site 2	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20240404	MGI			PMID:37797712
1558498	Mbtps2	membrane-bound transcription factor peptidase, site 2	gene	MP:0006433	abnormal articular cartilage morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:37797712
1558498	Mbtps2	membrane-bound transcription factor peptidase, site 2	gene	MP:0011692	increased chondrocyte number		IAGP		N	RGD:5509061	20240404	MGI			PMID:37797712
1558498	Mbtps2	membrane-bound transcription factor peptidase, site 2	gene	MP:0014025	decreased subchondral bone mineral content		IAGP		N	RGD:5509061	20240404	MGI			PMID:37797712
1558498	Mbtps2	membrane-bound transcription factor peptidase, site 2	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20240404	MGI			PMID:37797712
1558498	Mbtps2	membrane-bound transcription factor peptidase, site 2	gene	MP:0030486	abnormal osteocyte canaliculus morphology		IAGP		N	RGD:5509061	20240404	MGI			PMID:37797712
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0002079	increased circulating insulin level		IEA		N	RGD:5509061	20211021	MGI			
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20160929	MGI			PMID:24886454
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0003443	increased circulating glycerol level		IEA		N	RGD:5509061	20200514	MGI			
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20141003	MGI			
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0005296	abnormal humerus morphology		IEA		N	RGD:5509061	20141003	MGI			
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20160804	MGI			
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0005602	decreased angiogenesis		IAGP		N	RGD:5509061	20160929	MGI			PMID:24886454
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0010068	decreased red blood cell distribution width		IEA		N	RGD:5509061	20200514	MGI			
1558500	Dusp3	dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related)	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20201022	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20210128	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0000599	enlarged liver		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20210128	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:20439739
1558502	Atg7	autophagy related 7	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0000880	decreased Purkinje cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23095749
1558502	Atg7	autophagy related 7	gene	MP:0000965	abnormal sensory neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:20439739
1558502	Atg7	autophagy related 7	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0001263	weight loss		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20230720	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0001360	abnormal social investigation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25155956
1558502	Atg7	autophagy related 7	gene	MP:0001392	abnormal locomotor behavior		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20200310	MGI			PMID:20439739
1558502	Atg7	autophagy related 7	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210128	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1558502	Atg7	autophagy related 7	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210128	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20200310	MGI			PMID:29438013
1558502	Atg7	autophagy related 7	gene	MP:0002152	abnormal brain morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20439739
1558502	Atg7	autophagy related 7	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:20439739
1558502	Atg7	autophagy related 7	gene	MP:0002662	abnormal cauda epididymis morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0002965	increased circulating serum albumin level		IEA		N	RGD:5509061	20210826	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0002968	increased circulating alkaline phosphatase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0003051	curly tail		IAGP		N	RGD:5509061	20200310	MGI			PMID:20439739
1558502	Atg7	autophagy related 7	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:20439739
1558502	Atg7	autophagy related 7	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1558502	Atg7	autophagy related 7	gene	MP:0003325	decreased liver function		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24185898
1558502	Atg7	autophagy related 7	gene	MP:0003449	abnormal intestine goblet cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0004098	abnormal cerebellar granule cell morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0004542	impaired acrosome reaction		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0004843	abnormal Paneth cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20200310	MGI			PMID:29438013
1558502	Atg7	autophagy related 7	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20200310	MGI			PMID:20439739
1558502	Atg7	autophagy related 7	gene	MP:0005311	abnormal circulating amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0005332	abnormal amino acid level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0005405	axon degeneration		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0008008	early cellular replicative senescence		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0008045	decreased NK cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0008246	abnormal leukocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0008249	abnormal common lymphocyte progenitor cell morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1558502	Atg7	autophagy related 7	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25155956
1558502	Atg7	autophagy related 7	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0008770	decreased survivor rate		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1558502	Atg7	autophagy related 7	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0009378	abnormal endoplasmic reticulum morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0009387	abnormal epidermal pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0009388	abnormal epidermal melanocyte morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20200310	MGI			PMID:24089213
1558502	Atg7	autophagy related 7	gene	MP:0009936	abnormal dendritic spine morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:25155956
1558502	Atg7	autophagy related 7	gene	MP:0009972	absent hippocampus pyramidal cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0009975	absent cerebral cortex pyramidal cells		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0010632	cardiac muscle necrosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:29438013
1558502	Atg7	autophagy related 7	gene	MP:0010741	abnormal melanocyte proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0010763	abnormal hematopoietic stem cell physiology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21339326
1558502	Atg7	autophagy related 7	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:29438013
1558502	Atg7	autophagy related 7	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1558502	Atg7	autophagy related 7	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0011277	decreased tail pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0011568	decreased foot pigmentation		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20200310	MGI			PMID:25290687
1558502	Atg7	autophagy related 7	gene	MP:0011743	abnormal Golgi apparatus morphology		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0012434	decreased intestinal adenoma incidence		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0013219	abnormal substantia nigra pars compacta morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:23152632
1558502	Atg7	autophagy related 7	gene	MP:0013654	increased CD103-positive CD11b-low dendritic cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:26214133
1558502	Atg7	autophagy related 7	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20201231	MGI			PMID:33082312
1558502	Atg7	autophagy related 7	gene	MP:0014239	abnormal intracellular organelle morphology		IAGP		N	RGD:5509061	20230615	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0014341	abnormal hepatocyte mitochondrial morphology		IAGP		N	RGD:5509061	20240118	MGI			PMID:15866887
1558502	Atg7	autophagy related 7	gene	MP:0014812	abnormal brain physiology		IAGP		N	RGD:5509061	20251204	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20200310	MGI			PMID:25155956
1558502	Atg7	autophagy related 7	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20200310	MGI			PMID:29438013
1558502	Atg7	autophagy related 7	gene	MP:0030939	abnormal autophagosome formation		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:18083104
1558502	Atg7	autophagy related 7	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25155956
1558502	Atg7	autophagy related 7	gene	MP:0030940	impaired autophagy		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558502	Atg7	autophagy related 7	gene	MP:0031355	abnormal proacrosomal vesicle fusion		IAGP		N	RGD:5509061	20220303	MGI			PMID:24853953
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20231109	MGI			PMID:23637775
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000286	abnormal mitral valve morphology		IAGP		N	RGD:5509061	20240104	MGI			PMID:23637775
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20170105	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20170105	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20210128	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0001657	abnormal induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0001694	absent egg cylinders		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098913
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21357675
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0001696	failure to gastrulate		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098913
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098913
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:19098913
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002188	small heart		IEA		N	RGD:5509061	20170105	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002416	abnormal proerythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210520	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002606	increased basophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23576758
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002887	decreased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20170504	MGI			PMID:24735673
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0002989	small kidney		IEA		N	RGD:5509061	20170105	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0003077	abnormal cell cycle		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392792
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0003216	absence seizures		IAGP		N	RGD:5509061	20170504	MGI			PMID:24735673
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0003641	small lung		IEA		N	RGD:5509061	20170105	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0003816	abnormal pituitary gland development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392792
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0003965	abnormal pituitary hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392792
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0003969	abnormal luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392792
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0003997	tonic-clonic seizures		IAGP		N	RGD:5509061	20170504	MGI			PMID:24735673
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0004810	decreased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0004994	abnormal brain wave pattern		IAGP		N	RGD:5509061	20170504	MGI			PMID:24735673
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0005011	increased eosinophil cell number		IEA		N	RGD:5509061	20211021	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0005134	decreased thyroid-stimulating hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392792
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392792
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0005152	pancytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098913
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0008813	decreased common myeloid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0009416	cardiac muscle degeneration		IAGP		N	RGD:5509061	20231109	MGI			PMID:23637775
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0009767	decreased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20170504	MGI			PMID:24735673
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20160421	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20231109	MGI			PMID:23637775
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0010418	perimembraneous ventricular septal defect		IAGP		N	RGD:5509061	20240125	MGI			PMID:23637775
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:23637775
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21357675
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17392792
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098913
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21357675
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011105	embryonic lethality between implantation and placentation, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21357675
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21357675
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20231109	MGI			PMID:23637775
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0011243	decreased fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23795291
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0020471	abnormal circadian behavior persistence		IAGP		N	RGD:5509061	20171012	MGI			PMID:24582500
1558503	Kdm1a	lysine (K)-specific demethylase 1A	gene	MP:0020476	abnormal circardian behavior entrainment		IAGP		N	RGD:5509061	20171012	MGI			PMID:24582500
1558504	Cep43	centrosomal protein 43	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201022	MGI			
1558504	Cep43	centrosomal protein 43	gene	MP:0001516	abnormal motor coordination/balance		IEA		N	RGD:5509061	20211021	MGI			
1558504	Cep43	centrosomal protein 43	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20211021	MGI			
1558504	Cep43	centrosomal protein 43	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1558504	Cep43	centrosomal protein 43	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558505	Usp50	ubiquitin specific peptidase 50	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20170105	MGI			
1558505	Usp50	ubiquitin specific peptidase 50	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20211021	MGI			
1558505	Usp50	ubiquitin specific peptidase 50	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558506	Fahd2a	fumarylacetoacetate hydrolase domain containing 2A	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20160804	MGI			
1558506	Fahd2a	fumarylacetoacetate hydrolase domain containing 2A	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20160804	MGI			
1558506	Fahd2a	fumarylacetoacetate hydrolase domain containing 2A	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20160804	MGI			
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20180215	MGI			PMID:27562646
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20211021	MGI			
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180215	MGI			PMID:27562646
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035106
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0002802	abnormal discrimination learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035106
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035106
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035106
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20180215	MGI			PMID:27562646
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0004509	abnormal pelvic girdle bone morphology		IEA		N	RGD:5509061	20170105	MGI			
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035106
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20180215	MGI			PMID:27562646
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20180215	MGI			PMID:27562646
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0008924	decreased cerebellar granule cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035106
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23035106
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20210128	MGI			
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0012424	decreased alimentary system tumor incidence		IAGP		N	RGD:5509061	20180215	MGI			PMID:27562646
1558507	Tnik	TRAF2 and NCK interacting kinase	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:23035106
1558510	Ints1	integrator complex subunit 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1558510	Ints1	integrator complex subunit 1	gene	MP:0006204	embryonic lethality before implantation		IEA		N	RGD:5509061	20111116	MGI			
1558510	Ints1	integrator complex subunit 1	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16807365
1558515	Gdpd5	glycerophosphodiester phosphodiesterase domain containing 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20170105	MGI			
1558515	Gdpd5	glycerophosphodiester phosphodiesterase domain containing 5	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943603
1558515	Gdpd5	glycerophosphodiester phosphodiesterase domain containing 5	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943603
1558515	Gdpd5	glycerophosphodiester phosphodiesterase domain containing 5	gene	MP:0001914	hemorrhage		IEA		N	RGD:5509061	20250508	MGI			
1558515	Gdpd5	glycerophosphodiester phosphodiesterase domain containing 5	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943603
1558515	Gdpd5	glycerophosphodiester phosphodiesterase domain containing 5	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20201022	MGI			
1558515	Gdpd5	glycerophosphodiester phosphodiesterase domain containing 5	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21943603
1558515	Gdpd5	glycerophosphodiester phosphodiesterase domain containing 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20210826	MGI			
1558515	Gdpd5	glycerophosphodiester phosphodiesterase domain containing 5	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20190502	MGI			
1558517	Gpr150	G protein-coupled receptor 150	gene	MP:0001510	abnormal coat appearance		IEA		N	RGD:5509061	20240523	MGI			
1558517	Gpr150	G protein-coupled receptor 150	gene	MP:0002098	abnormal vibrissa morphology		IEA		N	RGD:5509061	20240523	MGI			
1558517	Gpr150	G protein-coupled receptor 150	gene	MP:0010511	shortened PR interval		IEA		N	RGD:5509061	20231207	MGI			
1558520	Ubl4a	ubiquitin-like 4A	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20161013	MGI			PMID:26195787
1558520	Ubl4a	ubiquitin-like 4A	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20161013	MGI			PMID:26195787
1558520	Ubl4a	ubiquitin-like 4A	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22139977
1558520	Ubl4a	ubiquitin-like 4A	gene	MP:0005438	abnormal glycogen homeostasis		IAGP		N	RGD:5509061	20161013	MGI			PMID:26195787
1558520	Ubl4a	ubiquitin-like 4A	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20161013	MGI			PMID:26195787
1558521	Gtf2h5	general transcription factor IIH, polypeptide 5	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23637614
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0000219	increased neutrophil cell number		IEA		N	RGD:5509061	20230601	MGI			
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20210128	MGI			
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20210128	MGI			
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210826	MGI			
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0002879	increased cellular sensitivity to X-ray irradiation induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0003644	thymus atrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0005016	decreased lymphocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0005018	decreased T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558522	Apex2	apurinic/apyrimidinic endonuclease 2	gene	MP:0009674	decreased birth weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15319281
1558524	Ncapd2	non-SMC condensin I complex, subunit D2	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20221201	MGI			PMID:34229059
1558524	Ncapd2	non-SMC condensin I complex, subunit D2	gene	MP:0008539	decreased susceptibility to induced colitis		IAGP		N	RGD:5509061	20221201	MGI			PMID:34229059
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0000157	abnormal sternum morphology		IEA		N	RGD:5509061	20230119	MGI			
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20230119	MGI			
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554939
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20230119	MGI			
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0003980	increased circulating phospholipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554939
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0004738	abnormal auditory brainstem response		IEA		N	RGD:5509061	20230119	MGI			
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0005178	increased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554939
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20230119	MGI			
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0010067	increased red blood cell distribution width		IEA		N	RGD:5509061	20230119	MGI			
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0010332	abnormal circulating apolipoprotein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554939
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0010333	abnormal circulating apolipoprotein E level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23554939
1558525	Osbpl8	oxysterol binding protein-like 8	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20230119	MGI			
1558526	Fzd8	frizzled class receptor 8	gene	MP:0000527	abnormal kidney development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21343368
1558526	Fzd8	frizzled class receptor 8	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21343368
1558526	Fzd8	frizzled class receptor 8	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20190502	MGI			
1558526	Fzd8	frizzled class receptor 8	gene	MP:0002989	small kidney		IAGP		N	RGD:5509061	20141003	MGI			PMID:21343368
1558526	Fzd8	frizzled class receptor 8	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20260402	MGI			
1558526	Fzd8	frizzled class receptor 8	gene	MP:0004936	impaired branching involved in ureteric bud morphogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21343368
1558526	Fzd8	frizzled class receptor 8	gene	MP:0005599	increased cardiac muscle contractility		IEA		N	RGD:5509061	20190502	MGI			
1558526	Fzd8	frizzled class receptor 8	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20250508	MGI			
1558526	Fzd8	frizzled class receptor 8	gene	MP:0010579	increased heart left ventricle size		IEA		N	RGD:5509061	20210128	MGI			
1558526	Fzd8	frizzled class receptor 8	gene	MP:0011111	lethality during fetal growth through weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21343368
1558526	Fzd8	frizzled class receptor 8	gene	MP:0011960	abnormal eye anterior chamber depth		IEA		N	RGD:5509061	20211021	MGI			
1558527	Prpf18	pre-mRNA processing factor 18	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558527	Prpf18	pre-mRNA processing factor 18	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1558527	Prpf18	pre-mRNA processing factor 18	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20220519	MGI			
1558528	Sdk2	sidekick cell adhesion molecule 2	gene	MP:0005551	abnormal eye electrophysiology		IAGP		N	RGD:5509061	20151224	MGI			PMID:26287463
1558529	Gpr143	G protein-coupled receptor 143	gene	MP:0001332	abnormal optic nerve innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092754
1558529	Gpr143	G protein-coupled receptor 143	gene	MP:0002864	abnormal ocular fundus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092754
1558529	Gpr143	G protein-coupled receptor 143	gene	MP:0005075	abnormal melanosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092754
1558529	Gpr143	G protein-coupled receptor 143	gene	MP:0005101	abnormal ciliary body pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092754
1558529	Gpr143	G protein-coupled receptor 143	gene	MP:0005103	abnormal retina pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092754
1558529	Gpr143	G protein-coupled receptor 143	gene	MP:0005199	abnormal iris pigment epithelium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092754
1558529	Gpr143	G protein-coupled receptor 143	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11092754
1558530	Septin12	septin 12	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220324	MGI			PMID:25588830
1558530	Septin12	septin 12	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220714	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0005578	teratozoospermia		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0008280	abnormal male germ cell apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0008545	absent sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:25588830
1558530	Septin12	septin 12	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220324	MGI			PMID:25588830
1558530	Septin12	septin 12	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0009830	abnormal sperm connecting piece morphology		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0009834	abnormal sperm annulus morphology		IAGP		N	RGD:5509061	20220324	MGI			PMID:25588830
1558530	Septin12	septin 12	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19359518
1558530	Septin12	septin 12	gene	MP:0031013	abnormal egg activation		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558530	Septin12	septin 12	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20220811	MGI			PMID:35547809
1558531	Npm3	nucleoplasmin 3	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20201231	MGI			
1558531	Npm3	nucleoplasmin 3	gene	MP:0005560	decreased circulating glucose level		IEA		N	RGD:5509061	20170105	MGI			
1558531	Npm3	nucleoplasmin 3	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20220519	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:4784576
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12461648
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4784576
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0000439	enlarged cranium		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0000743	muscle spasm		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4732188
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0000825	dilated lateral ventricle		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0000852	small cerebellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:12461648
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:4784576
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001867	rhinitis		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:12461648
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0001947	abnormal mucociliary clearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0002061	abnormal aggression-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:4784576
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0002065	abnormal fear/anxiety-related behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:4784576
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0002083	premature death		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0002133	abnormal respiratory system physiology		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0002653	abnormal ependyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4784576
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0003644	thymus atrophy		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0004421	enlarged parietal bone		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0005150	cachexia		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0005537	abnormal cerebral aqueduct morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:4732188
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:4784576
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0009022	abnormal brain meninges morphology		IEA		N	RGD:5509061	20111116	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0009804	abnormal brain interventricular foramen morphology		IEA		N	RGD:5509061	20161103	MGI			
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0011059	abnormal ependyma motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18250199
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12461648
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:12461648
1558533	Hydin	HYDIN, axonemal central pair apparatus protein	gene	MP:0030029	wide cranial sutures		IAGP		N	RGD:5509061	20170810	MGI			PMID:4784576
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0000026	abnormal inner ear morphology		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0000914	exencephaly		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0002947	increased hemangioma incidence		IEA		N	RGD:5509061	20210930	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0003686	abnormal eye muscle morphology		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0004269	abnormal optic cup morphology		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0004463	basisphenoid bone foramen		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0006063	abnormal inferior vena cava morphology		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0013834	thin hypoglossal nerve		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0013835	absent hypoglossal nerve		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0013836	abnormal hypoglossal nerve topology		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0013848	subcutaneous edema		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0013876	absent ductus venosus valve		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0013877	abnormal ductus venosus valve morphology		IEA		N	RGD:5509061	20171228	MGI			
1558535	Hmgxb3	HMG box domain containing 3	gene	MP:0013971	blood in lymph vessels		IEA		N	RGD:5509061	20171228	MGI			
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20200402	MGI			PMID:30338217
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20170105	MGI			
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0000371	diluted coat color		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0001179	thick pulmonary interalveolar septum		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200402	MGI			PMID:26885862
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20200402	MGI			PMID:30338217
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20200402	MGI			PMID:30338217
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0003917	increased kidney weight		IEA		N	RGD:5509061	20211021	MGI			
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0004721	abnormal platelet dense granule morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0004725	decreased platelet serotonin level		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0005172	decreased eye pigmentation		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0005606	increased bleeding time		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20200402	MGI			PMID:30338217
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0009448	decreased platelet ATP level		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0009549	decreased platelet aggregation		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0009557	decreased platelet ADP level		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0009709	hydrometra		IEA		N	RGD:5509061	20170105	MGI			
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0010815	enlarged alveolar lamellar bodies		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0010911	abnormal pulmonary acinus morphology		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20200402	MGI			PMID:30338217
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20200402	MGI			PMID:30338217
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0020432	decreased platelet dense granule number		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558536	Rab32	RAB32, member RAS oncogene family	gene	MP:0031120	decreased susceptibility to induced thrombosis		IAGP		N	RGD:5509061	20210121	MGI			PMID:31399401
1558537	Kif17	kinesin family member 17	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521616
1558537	Kif17	kinesin family member 17	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521616
1558537	Kif17	kinesin family member 17	gene	MP:0001475	reduced long-term depression		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521616
1558537	Kif17	kinesin family member 17	gene	MP:0001900	impaired synaptic plasticity		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521616
1558537	Kif17	kinesin family member 17	gene	MP:0001902	reduced NMDA-mediated synaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521616
1558537	Kif17	kinesin family member 17	gene	MP:0004768	abnormal axonal transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521616
1558537	Kif17	kinesin family member 17	gene	MP:0009454	impaired contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:21521616
1558537	Kif17	kinesin family member 17	gene	MP:0014367	impaired long-term object recognition memory		IAGP		N	RGD:5509061	20240328	MGI			PMID:21521616
1558540	Nop53	NOP53 ribosome biogenesis factor	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20170817	MGI			PMID:21804542
1558540	Nop53	NOP53 ribosome biogenesis factor	gene	MP:0011094	embryonic lethality before implantation, complete penetrance		IAGP		N	RGD:5509061	20170817	MGI			PMID:21804542
1558540	Nop53	NOP53 ribosome biogenesis factor	gene	MP:0020438	decreased papilloma incidence		IAGP		N	RGD:5509061	20170831	MGI			PMID:21804542
1558541	Septin11	septin 11	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20201022	MGI			
1558541	Septin11	septin 11	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20200409	MGI			PMID:21824005
1558541	Septin11	septin 11	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20200409	MGI			PMID:21824005
1558541	Septin11	septin 11	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20200514	MGI			
1558541	Septin11	septin 11	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1558541	Septin11	septin 11	gene	MP:0013294	prenatal lethality prior to heart atrial septation		IEA		N	RGD:5509061	20241121	MGI			
1558542	Zfyve16	zinc finger, FYVE domain containing 16	gene	MP:0005015	increased T cell number		IAGP		N	RGD:5509061	20210415	MGI			PMID:29247407
1558542	Zfyve16	zinc finger, FYVE domain containing 16	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20210415	MGI			PMID:29247407
1558542	Zfyve16	zinc finger, FYVE domain containing 16	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20210415	MGI			PMID:29247407
1558542	Zfyve16	zinc finger, FYVE domain containing 16	gene	MP:0013892	increased common lymphocyte progenitor cell number		IAGP		N	RGD:5509061	20210415	MGI			PMID:29247407
1558543	Pla2r1	phospholipase A2 receptor 1	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20211223	MGI			PMID:33594040
1558543	Pla2r1	phospholipase A2 receptor 1	gene	MP:0008734	decreased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:9407054
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0000186	decreased circulating HDL cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0000208	decreased hematocrit		IEA		N	RGD:5509061	20221215	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0000443	abnormal snout morphology		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20211021	MGI			PMID:32376790
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0001258	decreased body length		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20211021	MGI			PMID:32376790
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20211021	MGI			PMID:32376790
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0002792	abnormal retina vasculature morphology		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20211021	MGI			PMID:32376790
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0005179	decreased circulating cholesterol level		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0005344	increased circulating bilirubin level		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20221215	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:32376790
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0010097	abnormal retina blood vessel morphology		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20220811	MGI			
1558544	Bcorl1	BCL6 co-repressor-like 1	gene	MP:0030610	absent teeth		IEA		N	RGD:5509061	20240523	MGI			
1558545	Pla2g12b	phospholipase A2, group XIIB	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1558545	Pla2g12b	phospholipase A2, group XIIB	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912808
1558545	Pla2g12b	phospholipase A2, group XIIB	gene	MP:0000186	decreased circulating HDL cholesterol level		IAGP		N	RGD:5509061	20160929	MGI			PMID:27534441
1558545	Pla2g12b	phospholipase A2, group XIIB	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912808
1558545	Pla2g12b	phospholipase A2, group XIIB	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912808
1558545	Pla2g12b	phospholipase A2, group XIIB	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22912808
1558547	Cramp1	cramped chromatin regulator 1	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20111116	MGI			
1558547	Cramp1	cramped chromatin regulator 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20220519	MGI			
1558547	Cramp1	cramped chromatin regulator 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220519	MGI			
1558547	Cramp1	cramped chromatin regulator 1	gene	MP:0004258	abnormal placenta size		IEA		N	RGD:5509061	20220519	MGI			
1558547	Cramp1	cramped chromatin regulator 1	gene	MP:0009142	decreased prepulse inhibition		IEA		N	RGD:5509061	20220519	MGI			
1558547	Cramp1	cramped chromatin regulator 1	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20220519	MGI			
1558547	Cramp1	cramped chromatin regulator 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220519	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20181227	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0000438	abnormal cranium morphology		IEA		N	RGD:5509061	20210520	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20211021	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0002644	decreased circulating triglyceride level		IEA		N	RGD:5509061	20211021	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20210128	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0004613	fusion of vertebral arches		IEA		N	RGD:5509061	20210520	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0005012	decreased eosinophil cell number		IEA		N	RGD:5509061	20201022	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0008099	abnormal plasma cell differentiation		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0008497	decreased IgG2b level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0008805	decreased circulating amylase level		IEA		N	RGD:5509061	20181227	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0013025	increased Ly6C low monocyte number		IEA		N	RGD:5509061	20181227	MGI			
1558548	Wac	WW domain containing adaptor with coiled-coil	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20241212	MGI			PMID:37171241
1558549	Megf10	multiple EGF-like-domains 10	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20160929	MGI			PMID:27170117
1558549	Megf10	multiple EGF-like-domains 10	gene	MP:0005240	abnormal amacrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407321
1558549	Megf10	multiple EGF-like-domains 10	gene	MP:0006068	abnormal retina horizontal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22407321
1558549	Megf10	multiple EGF-like-domains 10	gene	MP:0008916	abnormal astrocyte physiology		IAGP		N	RGD:5509061	20160929	MGI			PMID:27170117
1558549	Megf10	multiple EGF-like-domains 10	gene	MP:0012261	increased hindbrain apoptosis		IAGP		N	RGD:5509061	20160929	MGI			PMID:27170117
1558550	Ptms	parathymosin	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20170105	MGI			
1558550	Ptms	parathymosin	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20220811	MGI			
1558550	Ptms	parathymosin	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20220811	MGI			
1558550	Ptms	parathymosin	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20260122	MGI			PMID:41241944
1558550	Ptms	parathymosin	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20260122	MGI			PMID:41241944
1558550	Ptms	parathymosin	gene	MP:0004924	abnormal behavior		IAGP		N	RGD:5509061	20260122	MGI			PMID:41241944
1558550	Ptms	parathymosin	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20260122	MGI			PMID:41241944
1558550	Ptms	parathymosin	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558550	Ptms	parathymosin	gene	MP:0011436	decreased urine magnesium level		IEA		N	RGD:5509061	20240523	MGI			
1558550	Ptms	parathymosin	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20260122	MGI			PMID:41241944
1558550	Ptms	parathymosin	gene	MP:0012506	brain atrophy		IAGP		N	RGD:5509061	20260122	MGI			PMID:41241944
1558550	Ptms	parathymosin	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20201022	MGI			
1558551	Dtna	dystrobrevin alpha	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558551	Dtna	dystrobrevin alpha	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558551	Dtna	dystrobrevin alpha	gene	MP:0000752	dystrophic muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719885
1558551	Dtna	dystrobrevin alpha	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10719885
1558551	Dtna	dystrobrevin alpha	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540561
1558551	Dtna	dystrobrevin alpha	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20240215	MGI			PMID:37461313
1558551	Dtna	dystrobrevin alpha	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558551	Dtna	dystrobrevin alpha	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558551	Dtna	dystrobrevin alpha	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558551	Dtna	dystrobrevin alpha	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558551	Dtna	dystrobrevin alpha	gene	MP:0003852	skeletal muscle necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558551	Dtna	dystrobrevin alpha	gene	MP:0004566	myocardial fiber degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558551	Dtna	dystrobrevin alpha	gene	MP:0004996	abnormal CNS synapse formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540561
1558551	Dtna	dystrobrevin alpha	gene	MP:0005330	cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558551	Dtna	dystrobrevin alpha	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540561
1558551	Dtna	dystrobrevin alpha	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10559919
1558552	Pdcl2	phosducin-like 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0001932	abnormal spermiogenesis		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0008839	absent acrosome		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0009232	abnormal sperm nucleus morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0009838	abnormal sperm axoneme morphology		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0020869	immotile sperm		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558552	Pdcl2	phosducin-like 2	gene	MP:0031354	abnormal acrosome assembly		IAGP		N	RGD:5509061	20231116	MGI			PMID:36278277
1558553	Acer3	alkaline ceramidase 3	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20180301	MGI			PMID:26474409
1558553	Acer3	alkaline ceramidase 3	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20180301	MGI			PMID:26474409
1558553	Acer3	alkaline ceramidase 3	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20180301	MGI			PMID:26474409
1558553	Acer3	alkaline ceramidase 3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180301	MGI			PMID:29401619
1558553	Acer3	alkaline ceramidase 3	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20180301	MGI			PMID:26474409
1558553	Acer3	alkaline ceramidase 3	gene	MP:0009823	abnormal sphingomyelin level		IAGP		N	RGD:5509061	20180301	MGI			PMID:26474409
1558553	Acer3	alkaline ceramidase 3	gene	MP:0012230	abnormal sphingolipid level		IAGP		N	RGD:5509061	20180301	MGI			PMID:26474409
1558553	Acer3	alkaline ceramidase 3	gene	MP:0012232	abnormal ceramide level		IAGP		N	RGD:5509061	20180301	MGI			PMID:26474409
1558553	Acer3	alkaline ceramidase 3	gene	MP:0020116	increased sphingosine level		IAGP		N	RGD:5509061	20180301	MGI			PMID:26474409
1558556	Suv39h1	suppressor of variegation 3-9 1	gene	MP:0001116	small gonad		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1558556	Suv39h1	suppressor of variegation 3-9 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1558556	Suv39h1	suppressor of variegation 3-9 1	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1558556	Suv39h1	suppressor of variegation 3-9 1	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1558556	Suv39h1	suppressor of variegation 3-9 1	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1558556	Suv39h1	suppressor of variegation 3-9 1	gene	MP:0005466	abnormal T-helper 2 physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763435
1558556	Suv39h1	suppressor of variegation 3-9 1	gene	MP:0005597	decreased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:22763435
1558556	Suv39h1	suppressor of variegation 3-9 1	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1558556	Suv39h1	suppressor of variegation 3-9 1	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:11701123
1558557	Tmbim1	transmembrane BAX inhibitor motif containing 1	gene	MP:0001570	abnormal circulating enzyme level		IAGP		N	RGD:5509061	20141003	MGI			PMID:16636500
1558557	Tmbim1	transmembrane BAX inhibitor motif containing 1	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:16636500
1558557	Tmbim1	transmembrane BAX inhibitor motif containing 1	gene	MP:0009873	abnormal aorta tunica media morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16607040
1558557	Tmbim1	transmembrane BAX inhibitor motif containing 1	gene	MP:0010574	dilated aorta		IAGP		N	RGD:5509061	20141003	MGI			PMID:16636500
1558558	Rbm6	RNA binding motif protein 6	gene	MP:0001392	abnormal locomotor behavior		IEA		N	RGD:5509061	20240523	MGI			
1558558	Rbm6	RNA binding motif protein 6	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1558558	Rbm6	RNA binding motif protein 6	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20240523	MGI			
1558558	Rbm6	RNA binding motif protein 6	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1558558	Rbm6	RNA binding motif protein 6	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20220811	MGI			
1558558	Rbm6	RNA binding motif protein 6	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20220811	MGI			
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159984
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0001798	impaired macrophage phagocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062524
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159984
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17486093
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159984
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062524
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159984
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159984
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0003883	enlarged stomach		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159984
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0004880	lung cyst		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159982
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159984
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062524
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0005399	increased susceptibility to fungal infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20062524
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0008588	abnormal circulating interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0008615	decreased circulating interleukin-17 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038916
1558559	Clec7a	C-type lectin domain family 7, member a	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:17159984
1558560	Tas2r138	taste receptor, type 2, member 138	gene	MP:0001513	limb grasping		IEA		N	RGD:5509061	20201231	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000238	absent pre-B cells		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509510
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000333	decreased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000334	decreased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968900
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968900
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968900
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000709	enlarged thymus		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000711	thymus cortex hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001601	abnormal myelopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001655	multifocal hepatic necrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001802	arrested B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968900
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968900
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509509
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509510
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002026	increased leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968900
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11870616
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509509
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002343	abnormal lymph node cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002348	abnormal lymph node medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002367	abnormal thymus lobule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002371	abnormal thymus cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002375	abnormal thymus medulla morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002458	abnormal B cell number		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509509
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509510
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002493	increased IgG level		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002606	increased basophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002722	abnormal immune system organ morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002831	absent Peyer's patches		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0003132	increased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0003133	increased early pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0003850	abnormal thymocyte activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0004977	increased B-1 B cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005015	increased T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11870616
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005017	decreased B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005018	decreased T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005061	abnormal eosinophil morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005068	abnormal NK cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005089	decreased double-negative T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968900
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005092	decreased double-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11870616
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005333	decreased heart rate		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0006410	abnormal common myeloid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008046	absent NK cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008046	absent NK cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008070	absent T cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008071	absent B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008075	decreased CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008078	increased CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008082	increased single-positive T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008083	decreased single-positive T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008102	lymph node hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008111	abnormal granulocyte differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008113	abnormal macrophage differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008124	decreased plasmacytoid dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008125	abnormal dendritic cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11870616
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008168	decreased B-1a cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008170	decreased B-1b cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11870616
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008170	decreased B-1b cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12479824
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008186	increased pro-B cell number		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509509
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008187	absent pro-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008187	absent pro-B cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008203	absent B-1a cells		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008208	decreased pro-B cell number		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509509
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509509
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008209	decreased pre-B cell number		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509510
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008211	decreased mature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008215	decreased immature B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008217	abnormal B cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11870616
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008346	increased gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008351	decreased gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008354	decreased mature gamma-delta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008463	abnormal peripheral lymph node morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20170713	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008465	absent mesenteric lymph nodes		IAGP		N	RGD:5509061	20170713	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008466	enlarged mesenteric lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008475	intermingled spleen red and white pulp		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008477	decreased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008478	increased spleen white pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:11870616
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008498	decreased IgG3 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:11870616
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008542	enlarged cervical lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7585946
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008760	abnormal immunoglobulin heavy chain V(D)J recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18538592
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008781	abnormal B cell apoptosis		IAGP		N	RGD:5509061	20151224	MGI			PMID:24509510
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008801	abnormal erythroid progenitor cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008941	reticulocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0008973	decreased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0009339	decreased splenocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0009395	increased nucleated erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0009622	absent inguinal lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0009630	absent axillary lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0009633	absent cervical lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0009633	absent cervical lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:8986714
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010130	decreased DN1 thymic pro-T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010132	decreased DN2 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010134	decreased DN3 thymocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010169	decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010336	increased acute lymphoblastic leukemia incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20393504
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010377	abnormal gut flora balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010841	increased central memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010844	increased effector memory CD4-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010847	increased central memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0010850	increased effector memory CD8-positive, alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:7923373
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0011176	abnormal erythroblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0011243	decreased fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0011400	lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0011719	abnormal natural killer cell mediated cytotoxicity		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0011816	decreased pre-pro B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:16968900
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24013668
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0013435	decreased CD8-positive, naive alpha-beta T cell number		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0014472	impaired B cell migration		IAGP		N	RGD:5509061	20240613	MGI			PMID:24509510
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0015015	impaired fetal liver erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:12871645
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0020002	increased response to antigen		IEA		N	RGD:5509061	20181011	MGI			
1558562	Ikzf1	IKAROS family zinc finger 1	gene	MP:0020155	enhanced humoral immune response		IEA		N	RGD:5509061	20181011	MGI			
1558563	Atg12	autophagy related 12	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:25585051
1558563	Atg12	autophagy related 12	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25585051
1558563	Atg12	autophagy related 12	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25585051
1558563	Atg12	autophagy related 12	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200310	MGI			PMID:25585051
1558563	Atg12	autophagy related 12	gene	MP:0008260	abnormal autophagy		IAGP		N	RGD:5509061	20200310	MGI			PMID:25585051
1558563	Atg12	autophagy related 12	gene	MP:0010024	increased total body fat amount		IAGP		N	RGD:5509061	20200310	MGI			PMID:25585051
1558563	Atg12	autophagy related 12	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:25585051
1558563	Atg12	autophagy related 12	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20200310	MGI			PMID:25585051
1558563	Atg12	autophagy related 12	gene	MP:0014142	increased body fat mass		IAGP		N	RGD:5509061	20200310	MGI			PMID:25585051
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000166	abnormal chondrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000554	abnormal carpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000572	abnormal autopod morphology		IEA		N	RGD:5509061	20230831	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0000601	small liver		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001147	small testis		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001157	small seminal vesicle		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15673568
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15673568
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20231207	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001319	irregularly shaped pupil		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001325	abnormal retina morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15673568
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20231207	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001919	abnormal reproductive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416163
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416163
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:16179923
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002110	abnormal digit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002115	abnormal limb bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002543	brachyphalangia		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002544	brachydactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002657	chondrodystrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002699	abnormal vitreous body morphology		IEA		N	RGD:5509061	20231207	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002825	abnormal notochord morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0002932	abnormal joint morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0003072	abnormal metatarsal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0003073	abnormal metacarpal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004351	short humerus		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004355	short radius		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004359	short ulna		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004634	short metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004635	short metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004639	fused metacarpal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004642	fused metatarsal bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0004703	abnormal vertebral column morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0005108	abnormal ulna morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0005201	abnormal retina pigment epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15673568
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0005225	abnormal vertebrae development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0005296	abnormal humerus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0005306	abnormal phalanx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631181
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0006280	abnormal digit development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12654290
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0008056	abnormal retina ganglion cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15673568
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0008258	thin endometrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416163
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0008259	abnormal optic disk morphology		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0008275	failure of endochondral bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0008730	fused phalanges		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416163
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0009097	absent endometrial glands		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416163
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0009250	abnormal appendicular skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16179923
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0009374	absent cumulus expansion		IAGP		N	RGD:5509061	20141003	MGI			PMID:11416163
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0009728	abnormal calcaneum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20230601	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0012281	decreased sternebra size		IAGP		N	RGD:5509061	20141003	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0013400	abnormal endometrial gland development		IAGP		N	RGD:5509061	20141218	MGI			PMID:11416163
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0014105	abnormal chondrocyte differentiation		IAGP		N	RGD:5509061	20171221	MGI			PMID:15781876
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0014291	decreased autopod size		IAGP		N	RGD:5509061	20230824	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0014750	abnormal retinal ganglion cell axon guidance		IAGP		N	RGD:5509061	20250904	MGI			PMID:12654290
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20231207	MGI			
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:12654290
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0030005	increased retina apoptosis		IAGP		N	RGD:5509061	20170706	MGI			PMID:15673568
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0030843	elbow dislocation		IAGP		N	RGD:5509061	20181025	MGI			PMID:10631182
1558564	Bmpr1b	bone morphogenetic protein receptor, type 1B	gene	MP:0030886	decreased radius size		IAGP		N	RGD:5509061	20181101	MGI			PMID:15781876
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20230601	MGI			
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0004398	cochlear inner hair cell degeneration		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0004527	abnormal outer hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0004532	abnormal inner hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0004533	fused inner hair cell stereocilia		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0004536	short inner hair cell stereocilia		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0004736	abnormal distortion product otoacoustic emission		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0011967	increased or absent threshold for auditory brainstem response		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558565	Elmod3	ELMO/CED-12 domain containing 3	gene	MP:0020849	abnormal actin cytoskeleton morphology		IAGP		N	RGD:5509061	20201001	MGI			PMID:31628468
1558566	Spen	spen family transcription repressor	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594956
1558566	Spen	spen family transcription repressor	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594956
1558566	Spen	spen family transcription repressor	gene	MP:0000601	small liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594956
1558566	Spen	spen family transcription repressor	gene	MP:0000771	abnormal brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594956
1558566	Spen	spen family transcription repressor	gene	MP:0001454	abnormal cued conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0001469	abnormal contextual conditioning behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0002063	abnormal learning/memory/conditioning		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0002144	abnormal B cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594956
1558566	Spen	spen family transcription repressor	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0003934	abnormal pancreas development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594956
1558566	Spen	spen family transcription repressor	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0008174	decreased follicular B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0008181	increased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17457934
1558566	Spen	spen family transcription repressor	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12594956
1558567	Ppef1	protein phosphatase with EF hand calcium-binding domain 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:11713293
1558568	Maco1	macoilin 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0000367	abnormal coat/ hair morphology		IEA		N	RGD:5509061	20250508	MGI			
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0000859	abnormal somatosensory cortex morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0001406	abnormal gait		IEA		N	RGD:5509061	20250508	MGI			
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0001529	abnormal vocalization		IEA		N	RGD:5509061	20250508	MGI			
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20250508	MGI			
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1558572	Tubb2a	tubulin, beta 2A class IIA	gene	MP:0012448	abnormal primary motor cortex morphology		IAGP		N	RGD:5509061	20210304	MGI			PMID:31386652
1558574	Lamb3	laminin, beta 3	gene	MP:0000764	abnormal tongue epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271670
1558574	Lamb3	laminin, beta 3	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271670
1558574	Lamb3	laminin, beta 3	gene	MP:0001208	blistering		IAGP		N	RGD:5509061	20160304	MGI			PMID:25350318
1558574	Lamb3	laminin, beta 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160304	MGI			PMID:25350318
1558574	Lamb3	laminin, beta 3	gene	MP:0002060	abnormal skin morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25350318
1558574	Lamb3	laminin, beta 3	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20160421	MGI			
1558574	Lamb3	laminin, beta 3	gene	MP:0002251	abnormal nasopharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271670
1558574	Lamb3	laminin, beta 3	gene	MP:0002252	abnormal oropharynx morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271670
1558574	Lamb3	laminin, beta 3	gene	MP:0009931	abnormal skin appearance		IAGP		N	RGD:5509061	20160304	MGI			PMID:25350318
1558574	Lamb3	laminin, beta 3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20160304	MGI			PMID:25350318
1558574	Lamb3	laminin, beta 3	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271670
1558574	Lamb3	laminin, beta 3	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160304	MGI			PMID:25350318
1558574	Lamb3	laminin, beta 3	gene	MP:0011159	abnormal epidermal-dermal junction morphology		IAGP		N	RGD:5509061	20160304	MGI			PMID:25350318
1558574	Lamb3	laminin, beta 3	gene	MP:0011160	dermal-epidermal separation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9271670
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0001364	decreased anxiety-related response		IEA		N	RGD:5509061	20220519	MGI			
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20220519	MGI			
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20220901	MGI			PMID:29253101
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20220519	MGI			
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0003313	abnormal locomotor activation		IEA		N	RGD:5509061	20260402	MGI			
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20220901	MGI			PMID:29253101
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20220519	MGI			
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20241121	MGI			
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0008428	abnormal spatial working memory		IEA		N	RGD:5509061	20260402	MGI			
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0013189	abnormal exploration in a new environment		IEA		N	RGD:5509061	20260402	MGI			
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20221215	MGI			
1558576	Zfhx2	zinc finger homeobox 2	gene	MP:0020955	increased mechanical nociceptive threshold		IAGP		N	RGD:5509061	20220901	MGI			PMID:29253101
1558577	Irx6	Iroquois homeobox 6	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20200402	MGI			
1558577	Irx6	Iroquois homeobox 6	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20211021	MGI			
1558577	Irx6	Iroquois homeobox 6	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20200402	MGI			
1558577	Irx6	Iroquois homeobox 6	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20200402	MGI			
1558577	Irx6	Iroquois homeobox 6	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20190808	MGI			
1558577	Irx6	Iroquois homeobox 6	gene	MP:0003734	abnormal retina inner plexiform layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172916
1558577	Irx6	Iroquois homeobox 6	gene	MP:0004021	abnormal rod electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172916
1558577	Irx6	Iroquois homeobox 6	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172916
1558577	Irx6	Iroquois homeobox 6	gene	MP:0006073	abnormal retina bipolar cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23172916
1558577	Irx6	Iroquois homeobox 6	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20201231	MGI			
1558580	Ubp1	upstream binding protein 1	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20200402	MGI			
1558580	Ubp1	upstream binding protein 1	gene	MP:0000260	abnormal angiogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0000292	distended pericardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20200402	MGI			
1558580	Ubp1	upstream binding protein 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0001718	abnormal visceral yolk sac morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0001722	pale yolk sac		IEA		N	RGD:5509061	20210520	MGI			
1558580	Ubp1	upstream binding protein 1	gene	MP:0001723	disorganized yolk sac vascular plexus		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20200402	MGI			
1558580	Ubp1	upstream binding protein 1	gene	MP:0003717	pallor		IEA		N	RGD:5509061	20210520	MGI			
1558580	Ubp1	upstream binding protein 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20210520	MGI			
1558580	Ubp1	upstream binding protein 1	gene	MP:0005553	increased circulating creatinine level		IEA		N	RGD:5509061	20211021	MGI			
1558580	Ubp1	upstream binding protein 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15282311
1558580	Ubp1	upstream binding protein 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558580	Ubp1	upstream binding protein 1	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20201231	MGI			
1558585	Cbx2	chromobox 2	gene	MP:0000120	malocclusion		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0000149	abnormal scapula morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0000495	abnormal colon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0001259	abnormal body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0001289	persistence of hyaloid vascular system		IEA		N	RGD:5509061	20160421	MGI			
1558585	Cbx2	chromobox 2	gene	MP:0001825	arrested T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0001939	secondary sex reversal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0002211	abnormal primary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0002212	abnormal secondary sex determination		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0002213	true hermaphroditism		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0003345	decreased rib number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0004607	abnormal cervical atlas morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0005644	agonadal		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0009335	decreased splenocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20210128	MGI			
1558585	Cbx2	chromobox 2	gene	MP:0010728	fusion of atlas and occipital bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9641679
1558585	Cbx2	chromobox 2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558585	Cbx2	chromobox 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558585	Cbx2	chromobox 2	gene	MP:0012283	decreased sternebra number		IAGP		N	RGD:5509061	20141003	MGI			PMID:9043087
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000111	cleft palate		IEA		N	RGD:5509061	20210520	MGI			
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000633	abnormal pituitary gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000780	abnormal corpus callosum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0000936	small embryonic telencephalon		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0001286	abnormal eye development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0002196	absent corpus callosum		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0002237	abnormal nasal cavity morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0003232	abnormal forebrain development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0003425	abnormal optic vesicle formation		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0003743	abnormal facial morphology		IEA		N	RGD:5509061	20210520	MGI			
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0004096	abnormal midbrain-hindbrain boundary development		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0004163	abnormal adenohypophysis morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0004269	abnormal optic cup morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0004309	absent otic vesicle		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0005193	abnormal anterior eye segment morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0006198	enophthalmos		IAGP		N	RGD:5509061	20171019	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0006292	abnormal nasal placode morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0006306	abnormal nasal pit morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0008219	abnormal dorsal telencephalic commissure morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0008223	absent hippocampal commissure		IAGP		N	RGD:5509061	20160526	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0008225	abnormal anterior commissure morphology		IAGP		N	RGD:5509061	20141218	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0008227	absent anterior commissure		IAGP		N	RGD:5509061	20141218	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0008321	small adenohypophysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0008789	abnormal olfactory epithelium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0008797	facial cleft		IEA		N	RGD:5509061	20210520	MGI			
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0009901	abnormal frontonasal prominence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0010059	olfactory bulb hypoplasia		IAGP		N	RGD:5509061	20171019	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20210128	MGI			
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0011495	abnormal head shape		IEA		N	RGD:5509061	20210520	MGI			
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0011759	absent Rathke's pouch		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0012004	abnormal septum pellucidum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17360769
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22007134
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0012138	decreased forebrain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0012178	absent frontonasal prominence		IAGP		N	RGD:5509061	20171019	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0012703	decreased embryonic neuroepithelium thickness		IAGP		N	RGD:5509061	20141003	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0013342	bifurcated Rathke's pouch		IAGP		N	RGD:5509061	20141204	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0013351	abnormal Rathke's pouch development		IAGP		N	RGD:5509061	20141218	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0013356	ectopic pituitary gland		IAGP		N	RGD:5509061	20141218	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0013357	ectopic adenohypophysis		IAGP		N	RGD:5509061	20141218	MGI			PMID:19093031
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0013597	small vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:9620767
1558586	Hesx1	homeobox gene expressed in ES cells	gene	MP:0014198	absent pituitary infundibular stalk		IAGP		N	RGD:5509061	20160526	MGI			PMID:9620767
1558587	Gdf2	growth differentiation factor 2	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558587	Gdf2	growth differentiation factor 2	gene	MP:0001879	abnormal lymphatic vessel morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558587	Gdf2	growth differentiation factor 2	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20210128	MGI			
1558587	Gdf2	growth differentiation factor 2	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22566602
1558587	Gdf2	growth differentiation factor 2	gene	MP:0002792	abnormal retina vasculature morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558587	Gdf2	growth differentiation factor 2	gene	MP:0004038	lymphangiectasis		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558587	Gdf2	growth differentiation factor 2	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22566602
1558587	Gdf2	growth differentiation factor 2	gene	MP:0006093	arteriovenous malformation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22566602
1558587	Gdf2	growth differentiation factor 2	gene	MP:0010097	abnormal retina blood vessel morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558587	Gdf2	growth differentiation factor 2	gene	MP:0010098	abnormal retina blood vessel pattern		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558588	Timm17b	translocase of inner mitochondrial membrane 17b	gene	MP:0000198	decreased circulating phosphate level		IEA		N	RGD:5509061	20241121	MGI			
1558588	Timm17b	translocase of inner mitochondrial membrane 17b	gene	MP:0005635	decreased circulating bilirubin level		IEA		N	RGD:5509061	20240523	MGI			
1558589	Actrt1	actin-related protein T1	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20211021	MGI			PMID:34422805
1558589	Actrt1	actin-related protein T1	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20211021	MGI			PMID:34422805
1558589	Actrt1	actin-related protein T1	gene	MP:0009234	absent sperm head		IAGP		N	RGD:5509061	20211021	MGI			PMID:34422805
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160526	MGI			PMID:24928897
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210128	MGI			
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0001325	abnormal retina morphology		IEA		N	RGD:5509061	20240523	MGI			
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20150924	MGI			PMID:20203623
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20150924	MGI			PMID:20203623
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20150924	MGI			PMID:20203623
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0004769	abnormal synaptic vesicle morphology		IAGP		N	RGD:5509061	20150924	MGI			PMID:20203623
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0004770	abnormal synaptic vesicle recycling		IAGP		N	RGD:5509061	20150924	MGI			PMID:20203623
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0004792	abnormal synaptic vesicle number		IAGP		N	RGD:5509061	20150924	MGI			PMID:20203623
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0004793	abnormal synaptic vesicle clustering		IAGP		N	RGD:5509061	20150924	MGI			PMID:20203623
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0005566	decreased blood urea nitrogen level		IEA		N	RGD:5509061	20260402	MGI			
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0006243	impaired pupillary reflex		IEA		N	RGD:5509061	20210128	MGI			
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0006320	abnormal interscapular fat pad morphology		IAGP		N	RGD:5509061	20160526	MGI			PMID:24928897
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20160526	MGI			PMID:24928897
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0009289	decreased epididymal fat pad weight		IAGP		N	RGD:5509061	20160526	MGI			PMID:24928897
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20160526	MGI			PMID:24928897
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0011167	abnormal adipose tissue development		IAGP		N	RGD:5509061	20160526	MGI			PMID:24928897
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20160526	MGI			PMID:24928897
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0011174	lipodystrophy		IAGP		N	RGD:5509061	20160526	MGI			PMID:24928897
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20150924	MGI			PMID:20203623
1558591	Ap1s2	adaptor-related protein complex 1, sigma 2 subunit	gene	MP:0013278	decreased fasting circulating glucose level		IEA		N	RGD:5509061	20211021	MGI			
1558593	Cxcl16	C-X-C motif chemokine ligand 16	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056360
1558593	Cxcl16	C-X-C motif chemokine ligand 16	gene	MP:0003721	increased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056360
1558593	Cxcl16	C-X-C motif chemokine ligand 16	gene	MP:0008040	decreased NK T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056360
1558593	Cxcl16	C-X-C motif chemokine ligand 16	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056360
1558593	Cxcl16	C-X-C motif chemokine ligand 16	gene	MP:0008578	decreased circulating interferon-gamma level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056360
1558593	Cxcl16	C-X-C motif chemokine ligand 16	gene	MP:0008603	decreased circulating interleukin-4 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056360
1558593	Cxcl16	C-X-C motif chemokine ligand 16	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056360
1558593	Cxcl16	C-X-C motif chemokine ligand 16	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:18056360
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522123
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000269	abnormal heart looping		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522123
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508520
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10603357
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508520
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000556	abnormal hindlimb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:10603357
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000729	abnormal myogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10603357
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508520
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000756	forelimb paralysis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508520
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15653949
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956886
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000846	abnormal medulla oblongata morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475798
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20141003	MGI			PMID:12358782
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956886
1558594	Lbx1	ladybird homeobox 1	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522123
1558594	Lbx1	ladybird homeobox 1	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12358782
1558594	Lbx1	ladybird homeobox 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956886
1558594	Lbx1	ladybird homeobox 1	gene	MP:0002746	abnormal semilunar valve morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475798
1558594	Lbx1	ladybird homeobox 1	gene	MP:0002948	abnormal neuron specification		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475798
1558594	Lbx1	ladybird homeobox 1	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522123
1558594	Lbx1	ladybird homeobox 1	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10508520
1558594	Lbx1	ladybird homeobox 1	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:10603357
1558594	Lbx1	ladybird homeobox 1	gene	MP:0003090	abnormal muscle precursor cell migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956886
1558594	Lbx1	ladybird homeobox 1	gene	MP:0003245	abnormal GABAergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234809
1558594	Lbx1	ladybird homeobox 1	gene	MP:0003247	abnormal glutaminergic neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16234809
1558594	Lbx1	ladybird homeobox 1	gene	MP:0003994	abnormal dorsal spinal root morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12358782
1558594	Lbx1	ladybird homeobox 1	gene	MP:0004610	small vertebrae		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0004704	short vertebral column		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0004819	decreased skeletal muscle mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:10603357
1558594	Lbx1	ladybird homeobox 1	gene	MP:0005277	abnormal brainstem morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475798
1558594	Lbx1	ladybird homeobox 1	gene	MP:0006006	increased sensory neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475798
1558594	Lbx1	ladybird homeobox 1	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12358782
1558594	Lbx1	ladybird homeobox 1	gene	MP:0006282	abnormal spinal cord dorsal horn morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0006284	absent hypaxial muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:10603357
1558594	Lbx1	ladybird homeobox 1	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15769945
1558594	Lbx1	ladybird homeobox 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17475798
1558594	Lbx1	ladybird homeobox 1	gene	MP:0010551	abnormal coronary vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522123
1558594	Lbx1	ladybird homeobox 1	gene	MP:0010724	thick interventricular septum		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522123
1558594	Lbx1	ladybird homeobox 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21956886
1558594	Lbx1	ladybird homeobox 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10603357
1558594	Lbx1	ladybird homeobox 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12522123
1558594	Lbx1	ladybird homeobox 1	gene	MP:0021094	abnormal dorsal interneuron 3 morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0021095	abnormal dorsal interneuron 4 morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0021096	abnormal dorsal interneuron 5 morphology		IAGP		N	RGD:5509061	20220519	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0021157	increased heart left ventricle wall thickness		IAGP		N	RGD:5509061	20231109	MGI			PMID:34906895
1558594	Lbx1	ladybird homeobox 1	gene	MP:0021206	abnormal limb muscle morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:10508520
1558594	Lbx1	ladybird homeobox 1	gene	MP:0021206	abnormal limb muscle morphology		IAGP		N	RGD:5509061	20221201	MGI			PMID:10603357
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20240502	MGI			PMID:38546043
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20240502	MGI			PMID:38546043
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0008014	increased lung tumor incidence		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0008564	increased interferon-beta secretion		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0008573	increased circulating interferon-alpha level		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0008575	increased circulating interferon-beta level		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0010767	abnormal female meiosis I arrest		IAGP		N	RGD:5509061	20240502	MGI			PMID:38546043
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0014237	decreased tumor-free survival time		IAGP		N	RGD:5509061	20240829	MGI			PMID:36548081
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0014435	increased interferon level		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0020914	decreased susceptibility to Riboviria infection		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0020917	decreased susceptibility to Herpesvirales infection		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0020938	decreased susceptibility to Picornaviridae infection		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558595	Ube2s	ubiquitin-conjugating enzyme E2S	gene	MP:0031039	decreased susceptibility to Picornaviridae infection induced morbidity/mortality		IAGP		N	RGD:5509061	20240502	MGI			PMID:32814047
1558597	Phb2	prohibitin 2	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862609
1558597	Phb2	prohibitin 2	gene	MP:0001120	abnormal uterus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:15713652
1558597	Phb2	prohibitin 2	gene	MP:0001382	abnormal nursing		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862609
1558597	Phb2	prohibitin 2	gene	MP:0001933	abnormal litter size		IAGP		N	RGD:5509061	20200310	MGI			PMID:15713652
1558597	Phb2	prohibitin 2	gene	MP:0004047	abnormal milk composition		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862609
1558597	Phb2	prohibitin 2	gene	MP:0004904	increased uterus weight		IAGP		N	RGD:5509061	20200310	MGI			PMID:15713652
1558597	Phb2	prohibitin 2	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20200310	MGI			PMID:15713652
1558597	Phb2	prohibitin 2	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281461
1558597	Phb2	prohibitin 2	gene	MP:0006270	abnormal mammary gland growth during lactation		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862609
1558597	Phb2	prohibitin 2	gene	MP:0006271	abnormal involution of the mammary gland		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862609
1558597	Phb2	prohibitin 2	gene	MP:0008943	increased sensitivity to induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281461
1558597	Phb2	prohibitin 2	gene	MP:0009503	abnormal mammary gland duct morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862609
1558597	Phb2	prohibitin 2	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862609
1558597	Phb2	prohibitin 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15713652
1558597	Phb2	prohibitin 2	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281461
1558597	Phb2	prohibitin 2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20200310	MGI			PMID:15713652
1558597	Phb2	prohibitin 2	gene	MP:0011704	decreased fibroblast proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:18281461
1558597	Phb2	prohibitin 2	gene	MP:0014126	increased mammary gland apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:21862609
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0000600	liver hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690081
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21407177
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21407177
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690081
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286202
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690081
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21407177
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21407177
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0003306	small intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:24089213
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20141003	MGI			PMID:18286202
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690081
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21407177
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690081
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0004259	small placenta		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0004264	abnormal extraembryonic tissue physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20260423	MGI			PMID:37983957
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0005031	abnormal trophoblast layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21407177
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0005432	abnormal pro-B cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690081
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17765679
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0008803	abnormal placental labyrinth vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21407177
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0010331	abnormal apolipoprotein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21407177
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:10650002
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15690081
1558600	Ern1	endoplasmic reticulum to nucleus signalling 1	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19805353
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0000428	abnormal craniofacial morphology		IAGP		N	RGD:5509061	20180705	MGI			PMID:29666258
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20180705	MGI			PMID:29666258
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20180705	MGI			PMID:29666258
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0000929	open neural tube		IAGP		N	RGD:5509061	20180705	MGI			PMID:29666258
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0001764	abnormal homeostasis		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0003720	abnormal neural tube closure		IAGP		N	RGD:5509061	20180705	MGI			PMID:29666258
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0003978	decreased circulating carnitine level		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0003979	increased circulating carnitine level		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20180705	MGI			PMID:29666258
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0008784	craniorachischisis		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20180705	MGI			PMID:29666258
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0011230	abnormal folic acid level		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0030658	increased glycine level		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0030659	decreased glycine level		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558601	Slc25a32	solute carrier family 25, member 32	gene	MP:0030691	increased serine level		IAGP		N	RGD:5509061	20230907	MGI			PMID:35727412
1558602	Steap4	STEAP family member 4	gene	MP:0000180	abnormal circulating cholesterol level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0002970	abnormal white adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0005266	abnormal metabolism		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0005425	increased macrophage cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0005458	increased percent body fat/body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0030017	decreased adipocyte glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:17482547
1558602	Steap4	STEAP family member 4	gene	MP:0030022	decreased muscle cell glucose uptake		IAGP		N	RGD:5509061	20170803	MGI			PMID:17482547
1558603	Mcts1	malignant T cell amplified sequence 1	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20210128	MGI			
1558603	Mcts1	malignant T cell amplified sequence 1	gene	MP:0001297	microphthalmia		IEA		N	RGD:5509061	20210128	MGI			
1558603	Mcts1	malignant T cell amplified sequence 1	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20240523	MGI			
1558603	Mcts1	malignant T cell amplified sequence 1	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20210128	MGI			
1558603	Mcts1	malignant T cell amplified sequence 1	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20260402	MGI			
1558605	Sez6l2	seizure related 6 homolog like 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558605	Sez6l2	seizure related 6 homolog like 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558605	Sez6l2	seizure related 6 homolog like 2	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558605	Sez6l2	seizure related 6 homolog like 2	gene	MP:0003894	abnormal Purkinje cell innervation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558605	Sez6l2	seizure related 6 homolog like 2	gene	MP:0011268	biphasic excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558605	Sez6l2	seizure related 6 homolog like 2	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558605	Sez6l2	seizure related 6 homolog like 2	gene	MP:0011272	short excitatory postsynaptic current rise time		IAGP		N	RGD:5509061	20141003	MGI			PMID:16814779
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0000071	axial skeleton hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20211021	MGI			
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0000382	underdeveloped hair follicles		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0000761	thin diaphragm muscle		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0001078	abnormal phrenic nerve morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0001201	translucent skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0001244	thin dermal layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:10856223
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20141003	MGI			PMID:10856223
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0001463	abnormal spatial learning		IAGP		N	RGD:5509061	20141003	MGI			PMID:10856223
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0001522	impaired swimming		IAGP		N	RGD:5509061	20141003	MGI			PMID:10856223
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:10856223
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0002919	enhanced paired-pulse facilitation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10856223
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0002971	abnormal brown adipose tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0003008	enhanced long-term potentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:10856223
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0003359	hypaxial muscle hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20201022	MGI			
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0005162	carpoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20211021	MGI			
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0009404	centrally nucleated skeletal muscle fibers		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20201022	MGI			
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0010053	decreased grip strength		IEA		N	RGD:5509061	20201022	MGI			
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0010123	increased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0010934	increased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20160407	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16738228
1558606	Ptprd	protein tyrosine phosphatase receptor type D	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591907
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238603
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620960
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591907
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620960
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000703	abnormal thymus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0000704	abnormal thymus development		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238603
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001123	dilated uterus		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591907
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001314	cornea opacity		IEA		N	RGD:5509061	20260402	MGI			
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001780	decreased brown adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238603
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238603
1558608	Cbl	Cbl proto-oncogene	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238603
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591907
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620960
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002118	abnormal lipid homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238603
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002145	abnormal T cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002364	abnormal thymus size		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002407	abnormal double-negative T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002414	abnormal myeloblast morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591907
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591907
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002644	decreased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0002953	thick ventricular wall		IEA		N	RGD:5509061	20211021	MGI			
1558608	Cbl	Cbl proto-oncogene	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238603
1558608	Cbl	Cbl proto-oncogene	gene	MP:0003333	liver fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0003896	prolonged PR interval		IEA		N	RGD:5509061	20211021	MGI			
1558608	Cbl	Cbl proto-oncogene	gene	MP:0003948	abnormal gas homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0003960	increased lean body mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0004809	increased hematopoietic stem cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19620960
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005348	increased T cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005409	darkened coat color		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005505	thrombocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005533	increased body temperature		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005584	abnormal enzyme/coenzyme activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0006319	abnormal epididymal fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008037	abnormal T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12415267
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008074	increased CD4-positive, alpha-beta T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:15238603
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008083	decreased single-positive T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591907
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008476	increased spleen red pulp amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008826	abnormal splenic cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008827	abnormal thymus cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008828	abnormal lymph node cell ratio		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0008904	abnormal mammary fat pad morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:9671496
1558608	Cbl	Cbl proto-oncogene	gene	MP:0009069	dilated oviduct		IAGP		N	RGD:5509061	20141003	MGI			PMID:12591907
1558608	Cbl	Cbl proto-oncogene	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0009379	abnormal foot pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:17130487
1558608	Cbl	Cbl proto-oncogene	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20150402	MGI			PMID:12591907
1558608	Cbl	Cbl proto-oncogene	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0011109	lethality throughout fetal growth and development, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558608	Cbl	Cbl proto-oncogene	gene	MP:0011276	increased tail pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0011278	increased ear pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:16211006
1558608	Cbl	Cbl proto-oncogene	gene	MP:0011630	increased mitochondrial size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0011965	decreased total retina thickness		IEA		N	RGD:5509061	20260402	MGI			
1558608	Cbl	Cbl proto-oncogene	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:15520865
1558608	Cbl	Cbl proto-oncogene	gene	MP:0031619	increased skeletal muscle cell glucose uptake		IAGP		N	RGD:5509061	20240801	MGI			PMID:15520865
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0000812	abnormal dentate gyrus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0000814	absent dentate gyrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0000830	abnormal diencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0001270	distended abdomen		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479999
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0001961	abnormal reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479999
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141120	MGI			
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0002739	abnormal olfactory bulb development		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540508
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540508
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479999
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479999
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540508
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0004279	abnormal rostral migratory stream morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540508
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0006009	abnormal neuronal migration		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540508
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540508
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479999
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0006092	abnormal olfactory sensory neuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21452247
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0008267	abnormal hippocampus CA3 region morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0008547	abnormal neocortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:16971467
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:16540508
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19479999
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0011679	abnormal vomeronasal sensory neuron morphology		IAGP		N	RGD:5509061	20150319	MGI			PMID:21452247
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0013595	absent vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:21452247
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0013597	small vomeronasal organ		IAGP		N	RGD:5509061	20150319	MGI			PMID:21452247
1558609	Fezf1	Fez family zinc finger 1	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20180208	MGI			PMID:16971467
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0000116	abnormal tooth development		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0000352	decreased cell proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20014010
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0000358	abnormal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20014010
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20014010
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0002182	abnormal astrocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0003241	loss of cortex neurons		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0003861	abnormal nervous system development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0004981	decreased neuronal precursor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0008439	abnormal cortical plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0009655	abnormal secondary palate development		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0009904	tongue hypoplasia		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0009937	abnormal neuron differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22991445
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0011095	embryonic lethality between implantation and placentation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:20014010
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993285
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0012113	decreased inner cell mass proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:14993285
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0021166	delayed palatal shelf elevation		IAGP		N	RGD:5509061	20221006	MGI			PMID:35151207
1558610	Setdb1	SET domain, bifurcated 1	gene	MP:0021215	abnormal palatal mesenchymal cell proliferation		IAGP		N	RGD:5509061	20230302	MGI			PMID:35151207
1558615	Slamf1	signaling lymphocytic activation molecule family member 1	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17135325
1558615	Slamf1	signaling lymphocytic activation molecule family member 1	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123745
1558615	Slamf1	signaling lymphocytic activation molecule family member 1	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123745
1558615	Slamf1	signaling lymphocytic activation molecule family member 1	gene	MP:0005027	increased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:15123745
1558615	Slamf1	signaling lymphocytic activation molecule family member 1	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:15539156
1558615	Slamf1	signaling lymphocytic activation molecule family member 1	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17202343
1558615	Slamf1	signaling lymphocytic activation molecule family member 1	gene	MP:0020952	increased susceptibility to Paramyxoviridae infection		IAGP		N	RGD:5509061	20200430	MGI			PMID:17135325
1558616	Glra4	glycine receptor, alpha 4 subunit	gene	MP:0000182	increased circulating LDL cholesterol level		IEA		N	RGD:5509061	20210128	MGI			
1558618	Dcp2	decapping mRNA 2	gene	MP:0001750	increased circulating follicle stimulating hormone level		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1558618	Dcp2	decapping mRNA 2	gene	MP:0001751	increased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1558618	Dcp2	decapping mRNA 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1558618	Dcp2	decapping mRNA 2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20160421	MGI			
1558618	Dcp2	decapping mRNA 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:21070968
1558618	Dcp2	decapping mRNA 2	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1558618	Dcp2	decapping mRNA 2	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1558618	Dcp2	decapping mRNA 2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20181227	MGI			
1558618	Dcp2	decapping mRNA 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1558618	Dcp2	decapping mRNA 2	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1558618	Dcp2	decapping mRNA 2	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1558618	Dcp2	decapping mRNA 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558618	Dcp2	decapping mRNA 2	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20201022	MGI			PMID:32245620
1558619	Ctsb	cathepsin B	gene	MP:0000422	delayed hair appearance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0000604	amyloidosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17068745
1558619	Ctsb	cathepsin B	gene	MP:0000681	abnormal thyroid gland morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782676
1558619	Ctsb	cathepsin B	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0000876	Purkinje cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:23054835
1558619	Ctsb	cathepsin B	gene	MP:0000877	abnormal Purkinje cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23054835
1558619	Ctsb	cathepsin B	gene	MP:0001219	thick epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133781
1558619	Ctsb	cathepsin B	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0001516	abnormal motor coordination/balance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23054835
1558619	Ctsb	cathepsin B	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
1558619	Ctsb	cathepsin B	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0001870	salivary gland inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
1558619	Ctsb	cathepsin B	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133781
1558619	Ctsb	cathepsin B	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0003202	abnormal neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0003224	neuron degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133781
1558619	Ctsb	cathepsin B	gene	MP:0003448	abnormal tumor morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133781
1558619	Ctsb	cathepsin B	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
1558619	Ctsb	cathepsin B	gene	MP:0004155	decreased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:10995788
1558619	Ctsb	cathepsin B	gene	MP:0004696	abnormal thyroid follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782676
1558619	Ctsb	cathepsin B	gene	MP:0004697	abnormal thyroid follicular cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782676
1558619	Ctsb	cathepsin B	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20141003	MGI			PMID:19664906
1558619	Ctsb	cathepsin B	gene	MP:0005468	abnormal thyroid hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:12782676
1558619	Ctsb	cathepsin B	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:15472011
1558619	Ctsb	cathepsin B	gene	MP:0006043	decreased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133781
1558619	Ctsb	cathepsin B	gene	MP:0008284	abnormal hippocampus pyramidal cell layer		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558619	Ctsb	cathepsin B	gene	MP:0009828	increased tumor latency		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133781
1558619	Ctsb	cathepsin B	gene	MP:0010299	increased mammary gland tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20133781
1558619	Ctsb	cathepsin B	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12048238
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000194	increased circulating calcium level		IEA		N	RGD:5509061	20221215	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000276	heart right ventricle hypertrophy		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000284	double outlet right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000297	abnormal atrioventricular cushion morphology		IEA		N	RGD:5509061	20111116	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000432	abnormal head morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000439	enlarged cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000445	short snout		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000519	hydronephrosis		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000644	dextrocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000650	mesocardia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000689	abnormal spleen morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0000690	absent spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001544	abnormal cardiovascular system physiology		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001872	sinus inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20150813	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0001963	abnormal hearing physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0002625	heart left ventricle hypertrophy		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0002639	micrognathia		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0002766	situs inversus		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0003178	left pulmonary isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0003283	abnormal digestive organ placement		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0003446	renal hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0003675	kidney cyst		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0004017	duplex kidney		IEA		N	RGD:5509061	20111116	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0004110	transposition of great arteries		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0004113	abnormal aortic arch morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0004133	heterotaxia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0004157	interrupted aortic arch		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0004158	right aortic arch		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0005565	increased blood urea nitrogen level		IEA		N	RGD:5509061	20230601	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20231207	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0006061	right atrial isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0006063	abnormal inferior vena cava morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0008461	left atrial isomerism		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0009705	abnormal midgut morphology		IEA		N	RGD:5509061	20150813	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010405	ostium secundum atrial septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010406	common atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010412	atrioventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010413	complete atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010422	heart right ventricle hypoplasia		IEA		N	RGD:5509061	20150326	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010435	abnormal heart atrium and ventricle connection		IEA		N	RGD:5509061	20111201	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010440	anomalous pulmonary venous connection		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010441	total anomalous pulmonary venous connection		IEA		N	RGD:5509061	20150326	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010460	pulmonary artery hypoplasia		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010466	vascular ring		IEA		N	RGD:5509061	20150226	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010487	abnormal right subclavian artery morphology		IEA		N	RGD:5509061	20150326	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010607	common atrioventricular valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010808	right-sided stomach		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0010854	lung situs inversus		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011055	abnormal respiratory motile cilium physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011083	lethality at weaning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011249	abdominal situs inversus		IEA		N	RGD:5509061	20111201	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011250	abdominal situs ambiguus		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011252	situs inversus totalis		IEA		N	RGD:5509061	20111116	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011253	situs inversus with levocardia		IEA		N	RGD:5509061	20111201	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011254	superior-inferior ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:18037990
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011510	biventricular, discordant atrioventricular connection		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011511	biventricular, ambiguous atrioventricular connection		IEA		N	RGD:5509061	20111215	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011649	immotile respiratory cilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:11912187
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011667	double outlet right ventricle with atrioventricular septal defect		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0011683	dual inferior vena cava		IEA		N	RGD:5509061	20141003	MGI			
1558622	Dnah5	dynein, axonemal, heavy chain 5	gene	MP:0014185	cerebellum atrophy		IAGP		N	RGD:5509061	20161013	MGI			PMID:11912187
1558623	Itgb1bp2	integrin beta 1 binding protein 2	gene	MP:0004484	abnormal response of heart to induced stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496958
1558623	Itgb1bp2	integrin beta 1 binding protein 2	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:12496958
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000259	abnormal vascular development		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000277	abnormal heart shape		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000279	ventricular hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073151
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000284	double outlet right ventricle		IEA		N	RGD:5509061	20170209	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000291	enlarged pericardium		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000295	trabecula carnea hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073151
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0000298	absent atrioventricular cushions		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073151
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20201022	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0001719	absent vitelline blood vessels		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0001823	thymus hypoplasia		IEA		N	RGD:5509061	20170209	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0002192	hydrops fetalis		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0003051	curly tail		IEA		N	RGD:5509061	20170209	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0004068	dilated dorsal aorta		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0004076	abnormal vitelline vascular remodeling		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0004783	abnormal cardinal vein morphology		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0005292	improved glucose tolerance		IEA		N	RGD:5509061	20210128	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073151
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0005554	decreased circulating creatinine level		IEA		N	RGD:5509061	20170105	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0006093	arteriovenous malformation		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0008528	polycystic kidney		IEA		N	RGD:5509061	20170209	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0008816	petechiae		IEA		N	RGD:5509061	20170209	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0010417	subarterial ventricular septal defect		IEA		N	RGD:5509061	20170209	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0010460	pulmonary artery hypoplasia		IEA		N	RGD:5509061	20170209	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0010586	absent conotruncal ridges		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073151
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15073151
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558624	Bmp10	bone morphogenetic protein 10	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20160225	MGI			PMID:23812757
1558625	Nkx6-3	NK6 homeobox 3	gene	MP:0004137	abnormal gastric surface mucous cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347062
1558625	Nkx6-3	NK6 homeobox 3	gene	MP:0004139	abnormal gastric parietal cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347062
1558625	Nkx6-3	NK6 homeobox 3	gene	MP:0004732	decreased circulating gastrin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347062
1558625	Nkx6-3	NK6 homeobox 3	gene	MP:0008006	increased stomach pH		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347062
1558625	Nkx6-3	NK6 homeobox 3	gene	MP:0010803	abnormal stomach enteroendocrine cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18347062
1558626	Zfp536	zinc finger protein 536	gene	MP:0000947	convulsive seizures		IEA		N	RGD:5509061	20260402	MGI			
1558626	Zfp536	zinc finger protein 536	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20211021	MGI			
1558626	Zfp536	zinc finger protein 536	gene	MP:0001575	cyanosis		IEA		N	RGD:5509061	20210520	MGI			
1558626	Zfp536	zinc finger protein 536	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20201022	MGI			
1558626	Zfp536	zinc finger protein 536	gene	MP:0005388	respiratory system phenotype		IEA		N	RGD:5509061	20160811	MGI			
1558626	Zfp536	zinc finger protein 536	gene	MP:0005564	increased hemoglobin content		IEA		N	RGD:5509061	20190502	MGI			
1558626	Zfp536	zinc finger protein 536	gene	MP:0005641	increased mean corpuscular hemoglobin concentration		IEA		N	RGD:5509061	20160421	MGI			
1558626	Zfp536	zinc finger protein 536	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1558713	Ethm3_m	ethanol induced thermoregulation 3 (mouse)	qtl	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11773602
1558713	Ethm3_m	ethanol induced thermoregulation 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11773602
1558717	Ses1a_m	salmonella enteritidis susceptibility 1a (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12058254
1558718	Scpro9_m	Stem cell proliferation 9 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11698278
1558718	Scpro9_m	Stem cell proliferation 9 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11698278
1558720	Bpq8_m	blood pressure QTL 8 (mouse)	qtl	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20111116	MGI			PMID:14996992
1558720	Bpq8_m	blood pressure QTL 8 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14996992
1558722	Htas3_m	hypothermia due to alcohol sensitivity 3 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8169823
1558722	Htas3_m	hypothermia due to alcohol sensitivity 3 (mouse)	qtl	MP:0005443	abnormal ethanol metabolism		IAGP		N	RGD:5509061	20111116	MGI			PMID:8169823
1558722	Htas3_m	hypothermia due to alcohol sensitivity 3 (mouse)	qtl	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20111116	MGI			PMID:8169823
1558724	Manln19_m	mandible length 19 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1558724	Manln19_m	mandible length 19 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1558724	Manln19_m	mandible length 19 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1558724	Manln19_m	mandible length 19 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1558728	Idd25_m	insulin dependent diabetes susceptibility 25 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:16015371
1558728	Idd25_m	insulin dependent diabetes susceptibility 25 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16015371
1558729	Vacq3_m	voluntary alcohol consumption QTL 3 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558729	Vacq3_m	voluntary alcohol consumption QTL 3 (mouse)	qtl	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558729	Vacq3_m	voluntary alcohol consumption QTL 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104380
1558732	Mfiq2_m	M16 feed intake QTL 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558732	Mfiq2_m	M16 feed intake QTL 2 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558733	Mfeq1_m	M16 feed efficiency QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558733	Mfeq1_m	M16 feed efficiency QTL 1 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558735	Egq2_m	early growth QTL 2 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558735	Egq2_m	early growth QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558736	Swrl2_m	SWR lupus locus 2 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11739537
1558736	Swrl2_m	SWR lupus locus 2 (mouse)	qtl	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15693014
1558736	Swrl2_m	SWR lupus locus 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15693014
1558736	Swrl2_m	SWR lupus locus 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15693014
1558737	Vacq4_m	voluntary alcohol consumption QTL 4 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558737	Vacq4_m	voluntary alcohol consumption QTL 4 (mouse)	qtl	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558737	Vacq4_m	voluntary alcohol consumption QTL 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104380
1558738	W6q1_m	weight 6 weeks QTL 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558738	W6q1_m	weight 6 weeks QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558739	Lgaq2_m	late growth adjusted QTL 2 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558739	Lgaq2_m	late growth adjusted QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558740	Bpq9_m	blood pressure QTL 9 (mouse)	qtl	MP:0002842	increased systemic arterial blood pressure		IAGP		N	RGD:5509061	20111116	MGI			PMID:14996992
1558740	Bpq9_m	blood pressure QTL 9 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14996992
1558741	Ses10_m	salmonella enteritidis susceptibility 10 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15973461
1558741	Ses10_m	salmonella enteritidis susceptibility 10 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15973461
1558742	Ses4_m	salmonella enteritidis susceptibility 4 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15973461
1558742	Ses4_m	salmonella enteritidis susceptibility 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15973461
1558743	Kcal1_m	kilocalorie 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12388789
1558743	Kcal1_m	kilocalorie 1 (mouse)	qtl	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20130328	MGI			PMID:12388789
1558744	Salpa1_m	serum alkaline phosphatase activity 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15542033
1558744	Salpa1_m	serum alkaline phosphatase activity 1 (mouse)	qtl	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20120209	MGI			PMID:15542033
1558745	Tsiq1_m	T-cell secretion of IL-4 QTL 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15815685
1558745	Tsiq1_m	T-cell secretion of IL-4 QTL 1 (mouse)	qtl	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15815685
1558746	lla_m	lymphoma latency acceleration (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9209340
1558746	lla_m	lymphoma latency acceleration (mouse)	qtl	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20131227	MGI			PMID:8641972
1558746	lla_m	lymphoma latency acceleration (mouse)	qtl	MP:0012431	increased lymphoma incidence		IAGP		N	RGD:5509061	20131227	MGI			PMID:9209340
1558748	Vacq1_m	voluntary alcohol consumption QTL 1 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558748	Vacq1_m	voluntary alcohol consumption QTL 1 (mouse)	qtl	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558748	Vacq1_m	voluntary alcohol consumption QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104380
1558749	Psl3_m	promotion susceptibility QTL 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12782578
1558749	Psl3_m	promotion susceptibility QTL 3 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12782578
1558749	Psl3_m	promotion susceptibility QTL 3 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12782578
1558751	Bomd6_m	bone mineral density 6 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11697791
1558751	Bomd6_m	bone mineral density 6 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11697791
1558752	Bntq1_m	bone traits QTL 1 (mouse)	qtl	MP:0000008	increased white adipose tissue amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15619674
1558752	Bntq1_m	bone traits QTL 1 (mouse)	qtl	MP:0000558	abnormal tibia morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15619674
1558752	Bntq1_m	bone traits QTL 1 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15619674
1558752	Bntq1_m	bone traits QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15619674
1558752	Bntq1_m	bone traits QTL 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15619674
1558752	Bntq1_m	bone traits QTL 1 (mouse)	qtl	MP:0008158	increased diameter of femur		IAGP		N	RGD:5509061	20111116	MGI			PMID:15619674
1558753	Ath19_m	atherosclerosis 19 (mouse)	qtl	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14592847
1558753	Ath19_m	atherosclerosis 19 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14592847|PMID:17641228
1558753	Ath19_m	atherosclerosis 19 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20151218	MGI		Created by mouse qtl pipeline	PMID:14592847
1558754	Nsila1_m	novelty/stress induced locomotor activation 1 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1558754	Nsila1_m	novelty/stress induced locomotor activation 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1558755	Skmw7_m	skeletal muscle weight  7 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15687484
1558755	Skmw7_m	skeletal muscle weight  7 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15687484
1558755	Skmw7_m	skeletal muscle weight  7 (mouse)	qtl	MP:0009423	increased extensor digitorum longus weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558756	Tgct1_m	testicular germ cell tumor 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12566386
1558756	Tgct1_m	testicular germ cell tumor 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12566386
1558756	Tgct1_m	testicular germ cell tumor 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12566386
1558756	Tgct1_m	testicular germ cell tumor 1 (mouse)	qtl	MP:0006262	increased testis tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12566386
1558757	Eae34_m	experimental allergic encephalomyelitis susceptibility 34 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15917267
1558757	Eae34_m	experimental allergic encephalomyelitis susceptibility 34 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15917267
1558758	Kcal2_m	kilocalorie 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12388789
1558758	Kcal2_m	kilocalorie 2 (mouse)	qtl	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20130322	MGI			PMID:16946080
1558758	Kcal2_m	kilocalorie 2 (mouse)	qtl	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20130328	MGI			PMID:12388789
1558759	Ap4q_m	alcohol preference 4 QTL (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:9726281
1558759	Ap4q_m	alcohol preference 4 QTL (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9726281
1558760	Nsila4_m	novelty/stress induced locomotor activation 4 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1558760	Nsila4_m	novelty/stress induced locomotor activation 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1558761	Nsila5_m	novelty/stress induced locomotor activation 5 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1558761	Nsila5_m	novelty/stress induced locomotor activation 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1558763	Gct9_m	granulosa cell tumorigenesis 9 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15735010
1558763	Gct9_m	granulosa cell tumorigenesis 9 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15735010
1558763	Gct9_m	granulosa cell tumorigenesis 9 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15735010
1558763	Gct9_m	granulosa cell tumorigenesis 9 (mouse)	qtl	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20131227	MGI			PMID:15735010
1558764	Scpro10_m	Stem cell proliferation 10 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11698278
1558764	Scpro10_m	Stem cell proliferation 10 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11698278
1558765	Tesw1_m	testis weight 1 (mouse)	qtl	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11333241
1558765	Tesw1_m	testis weight 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11333241
1558765	Tesw1_m	testis weight 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11333241
1558766	Mmtp2_m	modifier of mammary tumor progression 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15859357
1558766	Mmtp2_m	modifier of mammary tumor progression 2 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:15859357
1558767	Skmw11_m	skeletal muscle weight  11 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15687484
1558767	Skmw11_m	skeletal muscle weight  11 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15687484
1558767	Skmw11_m	skeletal muscle weight  11 (mouse)	qtl	MP:0009423	increased extensor digitorum longus weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558767	Skmw11_m	skeletal muscle weight  11 (mouse)	qtl	MP:0009425	increased soleus weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558767	Skmw11_m	skeletal muscle weight  11 (mouse)	qtl	MP:0009427	increased tibialis anterior weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558767	Skmw11_m	skeletal muscle weight  11 (mouse)	qtl	MP:0009427	increased tibialis anterior weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1558768	Mfi7q1_m	M16 feed intake at 7 weeks QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558768	Mfi7q1_m	M16 feed intake at 7 weeks QTL 1 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558769	Zolw1_m	zolpidem withdrawal 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16436183
1558769	Zolw1_m	zolpidem withdrawal 1 (mouse)	qtl	MP:0009775	increased behavioral withdrawal response		IAGP		N	RGD:5509061	20111116	MGI			PMID:16436183
1558770	Mnif2_m	macronutrient intake, fat 2 (mouse)	qtl	MP:0001431	abnormal eating behavior		IAGP		N	RGD:5509061	20111116	MGI			PMID:12388789
1558770	Mnif2_m	macronutrient intake, fat 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12388789
1558771	Eae35_m	experimental allergic encephalomyelitis susceptibility 35 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15917267
1558771	Eae35_m	experimental allergic encephalomyelitis susceptibility 35 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15917267
1558772	Lith23_m	lithogenic gene 23 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:15834632
1558772	Lith23_m	lithogenic gene 23 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15834632
1558774	Lith17_m	lithogenic gene 17 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:15834632
1558774	Lith17_m	lithogenic gene 17 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151694|PMID:15834632
1558774	Lith17_m	lithogenic gene 17 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20150724	MGI		Created by mouse qtl pipeline	PMID:15834632
1558775	Eclc_m	epistatic circling C C57L/J 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11932245
1558776	Artmd1_m	arthropathy in MRL and DBA/1 mice 1 (mouse)	qtl	MP:0002936	joint swelling		IAGP		N	RGD:5509061	20111116	MGI			PMID:15751084
1558776	Artmd1_m	arthropathy in MRL and DBA/1 mice 1 (mouse)	qtl	MP:0003189	fused joints		IAGP		N	RGD:5509061	20111116	MGI			PMID:15751084
1558776	Artmd1_m	arthropathy in MRL and DBA/1 mice 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15751084
1558776	Artmd1_m	arthropathy in MRL and DBA/1 mice 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15751084
1558777	Marq2_m	methamphetamine response QTL 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104378
1558777	Marq2_m	methamphetamine response QTL 2 (mouse)	qtl	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104378
1558779	Eclb_m	epistatic circling B C57L/J (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11932245
1558780	Idd22_m	insulin dependent diabetes susceptibility 22 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:14513297
1558780	Idd22_m	insulin dependent diabetes susceptibility 22 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14513297
1558782	Orgwq9_m	organ weight QTL 9 (mouse)	qtl	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1558782	Orgwq9_m	organ weight QTL 9 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1558782	Orgwq9_m	organ weight QTL 9 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1558782	Orgwq9_m	organ weight QTL 9 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12118102
1558782	Orgwq9_m	organ weight QTL 9 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1558783	Idd26_m	insulin dependent diabetes susceptibility 26 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:16015371
1558783	Idd26_m	insulin dependent diabetes susceptibility 26 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16015371
1558785	Ablp_m	absorbance of eye lens protein (mouse)	qtl	MP:0005319	abnormal enzyme/coenzyme level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15519297
1558785	Ablp_m	absorbance of eye lens protein (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15519297
1558787	Cplaq8_m	circadian period of locomotor activity 8 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15332441
1558787	Cplaq8_m	circadian period of locomotor activity 8 (mouse)	qtl	MP:0020469	prolonged circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:15332441
1558788	Ptnu2_m	proteinuria 2 (mouse)	qtl	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15965785
1558788	Ptnu2_m	proteinuria 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15965785
1558788	Ptnu2_m	proteinuria 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15965785
1558790	Mmtp1_m	modifier of mammary tumor progression 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15859357
1558790	Mmtp1_m	modifier of mammary tumor progression 1 (mouse)	qtl	MP:0002166	abnormal tumor susceptibility		IAGP		N	RGD:5509061	20111116	MGI			PMID:15859357
1558790	Mmtp1_m	modifier of mammary tumor progression 1 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:15859357
1558791	Mlepq1_m	M16 leptin QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558791	Mlepq1_m	M16 leptin QTL 1 (mouse)	qtl	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558792	Htas4_m	hypothermia due to alcohol sensitivity 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8169823
1558792	Htas4_m	hypothermia due to alcohol sensitivity 4 (mouse)	qtl	MP:0005443	abnormal ethanol metabolism		IAGP		N	RGD:5509061	20111116	MGI			PMID:8169823
1558792	Htas4_m	hypothermia due to alcohol sensitivity 4 (mouse)	qtl	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20111116	MGI			PMID:8169823
1558793	Scc11_m	colon tumor susceptibility 11 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14562056
1558793	Scc11_m	colon tumor susceptibility 11 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:14562056
1558794	Agnm1_m	autoimmune glomerulonephritis in MRL 1 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15832294
1558794	Agnm1_m	autoimmune glomerulonephritis in MRL 1 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:15832294
1558794	Agnm1_m	autoimmune glomerulonephritis in MRL 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15832294
1558794	Agnm1_m	autoimmune glomerulonephritis in MRL 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15832294
1558796	Gsi2_m	glomerulsclerosis index 2 (mouse)	qtl	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:16093645
1558796	Gsi2_m	glomerulsclerosis index 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16093645
1558797	Scpro8_m	Stem cell proliferation 8 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11698278
1558797	Scpro8_m	Stem cell proliferation 8 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11698278
1558799	Nba4_m	New Zealand Black autoimmunity 4 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15693014
1558799	Nba4_m	New Zealand Black autoimmunity 4 (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15693014
1558799	Nba4_m	New Zealand Black autoimmunity 4 (mouse)	qtl	MP:0004771	increased anti-single stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15693014
1558799	Nba4_m	New Zealand Black autoimmunity 4 (mouse)	qtl	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12215897
1558799	Nba4_m	New Zealand Black autoimmunity 4 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15693014
1558799	Nba4_m	New Zealand Black autoimmunity 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15693014
1558799	Nba4_m	New Zealand Black autoimmunity 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15693014
1558799	Nba4_m	New Zealand Black autoimmunity 4 (mouse)	qtl	MP:0008502	increased IgG3 level		IAGP		N	RGD:5509061	20111116	MGI			PMID:12215897
1558801	Tsiq2_m	T-cell secretion of IL-4 QTL 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15815685
1558801	Tsiq2_m	T-cell secretion of IL-4 QTL 2 (mouse)	qtl	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15815685
1558802	Skmw6_m	skeletal muscle weight  6 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15687484
1558802	Skmw6_m	skeletal muscle weight  6 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15687484
1558802	Skmw6_m	skeletal muscle weight  6 (mouse)	qtl	MP:0009425	increased soleus weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558802	Skmw6_m	skeletal muscle weight  6 (mouse)	qtl	MP:0009425	increased soleus weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1558802	Skmw6_m	skeletal muscle weight  6 (mouse)	qtl	MP:0009427	increased tibialis anterior weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558802	Skmw6_m	skeletal muscle weight  6 (mouse)	qtl	MP:0009427	increased tibialis anterior weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1558803	W3q16_m	weight 3 weeks QTL 16 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558803	W3q16_m	weight 3 weeks QTL 16 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558805	Bodw3_m	body weight 3 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1558805	Bodw3_m	body weight 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558806	Vacq5_m	voluntary alcohol consumption QTL 5 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558806	Vacq5_m	voluntary alcohol consumption QTL 5 (mouse)	qtl	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558806	Vacq5_m	voluntary alcohol consumption QTL 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104380
1558807	Ceat1_m	chronic experimental autoimmune thyroiditis 1 (mouse)	qtl	MP:0002876	abnormal thyroid gland physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12086944
1558807	Ceat1_m	chronic experimental autoimmune thyroiditis 1 (mouse)	qtl	MP:0004825	increased susceptibility to experimental autoimmune thyroiditis		IAGP		N	RGD:5509061	20111116	MGI			PMID:12086944
1558807	Ceat1_m	chronic experimental autoimmune thyroiditis 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12086944
1558807	Ceat1_m	chronic experimental autoimmune thyroiditis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12086944
1558808	Kdw1_m	kidney weight 1 (mouse)	qtl	MP:0003918	decreased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16093645
1558808	Kdw1_m	kidney weight 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16093645
1558809	Lith20_m	lithogenic gene 20 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:15834632
1558809	Lith20_m	lithogenic gene 20 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15834632
1558811	Scc13_m	colon tumor susceptibility 13 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14562056
1558811	Scc13_m	colon tumor susceptibility 13 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:14562056
1558812	Rafar_m	retinoic acid induced forelimb autopod reduction (mouse)	qtl	MP:0000550	abnormal forelimb morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15781699
1558812	Rafar_m	retinoic acid induced forelimb autopod reduction (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15781699
1558813	Lmrq5_m	Leishmania major resistance QTL 5 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9175833
1558813	Lmrq5_m	Leishmania major resistance QTL 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9175833
1558814	Ducm1_m	dsRNA-induced UCM 1 (mouse)	qtl	MP:0002452	abnormal professional antigen presenting cell physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14625548
1558814	Ducm1_m	dsRNA-induced UCM 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14625548
1558815	Gstml_m	gestational survival modifier locus (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15649944
1558815	Gstml_m	gestational survival modifier locus (mouse)	qtl	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20111116	MGI			PMID:15649944
1558816	Bomd5_m	bone mineral density 5 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11697791
1558816	Bomd5_m	bone mineral density 5 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11697791
1558818	Asm1_m	autoimmune sialadenitis in MRL mice 1 (mouse)	qtl	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20111116	MGI			PMID:10616009
1558818	Asm1_m	autoimmune sialadenitis in MRL mice 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10616009
1558819	Ossc2_m	osteosarcoma susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11893245|PMID:16331598
1558819	Ossc2_m	osteosarcoma susceptibility 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20150807	MGI		Created by mouse qtl pipeline	PMID:11893245
1558819	Ossc2_m	osteosarcoma susceptibility 2 (mouse)	qtl	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11893245
1558820	Moo1_m	modifier of Odc1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16086382|PMID:11944982
1558820	Moo1_m	modifier of Odc1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20151023	MGI		Created by mouse qtl pipeline	PMID:11944982
1558820	Moo1_m	modifier of Odc1 (mouse)	qtl	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11944982
1558820	Moo1_m	modifier of Odc1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20160506	MGI		Created by mouse qtl pipeline	PMID:14693723
1558825	Aabpr_m	aberrant activation of B cell proliferation (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14695357
1558825	Aabpr_m	aberrant activation of B cell proliferation (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14695357
1558825	Aabpr_m	aberrant activation of B cell proliferation (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14695357
1558826	Spnw4_m	spleen weight 4 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1558826	Spnw4_m	spleen weight 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:16151693
1558826	Spnw4_m	spleen weight 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558826	Spnw4_m	spleen weight 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558828	Mfiq1_m	M16 feed intake QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558828	Mfiq1_m	M16 feed intake QTL 1 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558829	W3q2_m	weight 3 weeks QTL 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558829	W3q2_m	weight 3 weeks QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558830	Egaq2_m	early growth adjusted QTL 2 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558830	Egaq2_m	early growth adjusted QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558832	Lmrq2_m	Leishmania major resistance QTL 2 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9175833
1558832	Lmrq2_m	Leishmania major resistance QTL 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9175833
1558833	Erars2_m	erosive arthritis susceptibility 2 (mouse)	qtl	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15683449
1558833	Erars2_m	erosive arthritis susceptibility 2 (mouse)	qtl	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15683449
1558833	Erars2_m	erosive arthritis susceptibility 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15683449
1558833	Erars2_m	erosive arthritis susceptibility 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15683449
1558834	Swrl3_m	SWR lupus locus 3 (mouse)	qtl	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15693014
1558834	Swrl3_m	SWR lupus locus 3 (mouse)	qtl	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:11739537
1558834	Swrl3_m	SWR lupus locus 3 (mouse)	qtl	MP:0004796	increased anti-histone antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15693014
1558834	Swrl3_m	SWR lupus locus 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15693014
1558835	Bdw1_m	body weight 1 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16093645
1558835	Bdw1_m	body weight 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16093645
1558836	Dice1b_m	determination of interleukin 4 commitment 1b (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15596523
1558836	Dice1b_m	determination of interleukin 4 commitment 1b (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15596523
1558837	Marq1_m	methamphetamine response QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104378
1558837	Marq1_m	methamphetamine response QTL 1 (mouse)	qtl	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104378
1558838	Mfiq5_m	M16 feed intake QTL 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558838	Mfiq5_m	M16 feed intake QTL 5 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558842	Tailq2_m	tail length QTL 2 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558842	Tailq2_m	tail length QTL 2 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558843	Ecla_m	epistatic circling A C57L/J 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11932245
1558844	Lith15_m	lithogenic gene 15 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151694
1558844	Lith15_m	lithogenic gene 15 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151694
1558845	Alprf_m	alcohol preference (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:10719795
1558845	Alprf_m	alcohol preference (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10719795
1558846	Hfib2_m	hepatic fibrogenesis 2 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15995705
1558846	Hfib2_m	hepatic fibrogenesis 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20141003	MGI		Created by mouse qtl pipeline	PMID:15995705
1558848	Marq5_m	methamphetamine response QTL 5 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104378
1558848	Marq5_m	methamphetamine response QTL 5 (mouse)	qtl	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104378
1558849	W3q15_m	weight 3 weeks QTL 15 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558849	W3q15_m	weight 3 weeks QTL 15 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558850	Sgp3_m	serum gp70 production 3 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15634937
1558850	Sgp3_m	serum gp70 production 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15634937
1558852	Gnf2_m	growth and fatness 2 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15769905
1558852	Gnf2_m	growth and fatness 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15769905
1558852	Gnf2_m	growth and fatness 2 (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15769905
1558853	Knyw3_m	kidney weight 3 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1558853	Knyw3_m	kidney weight 3 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558853	Knyw3_m	kidney weight 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:16151693
1558855	Eae30_m	experimental allergic encephalomyelitis susceptibility 30 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15917267
1558855	Eae30_m	experimental allergic encephalomyelitis susceptibility 30 (mouse)	qtl	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20111116	MGI			PMID:15917267
1558856	Scc14_m	colon tumor susceptibility 14 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14562056
1558856	Scc14_m	colon tumor susceptibility 14 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:14562056
1558858	Scpro7_m	Stem cell proliferation 7 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11698278
1558858	Scpro7_m	Stem cell proliferation 7 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11698278
1558859	Vacq2_m	voluntary alcohol consumption QTL 2 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558859	Vacq2_m	voluntary alcohol consumption QTL 2 (mouse)	qtl	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558859	Vacq2_m	voluntary alcohol consumption QTL 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104380
1558860	W10q7_m	weight 10 weeks QTL 7 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558860	W10q7_m	weight 10 weeks QTL 7 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558862	Lmrq3_m	Leishmania major resistance QTL 3 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9175833
1558862	Lmrq3_m	Leishmania major resistance QTL 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9175833
1558863	Scpro5_m	Stem cell proliferation 5 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11698278
1558863	Scpro5_m	Stem cell proliferation 5 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15788535
1558863	Scpro5_m	Stem cell proliferation 5 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11698278
1558865	Lith21_m	lithogenic gene 21 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:15834632
1558865	Lith21_m	lithogenic gene 21 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15834632
1558866	Lmrq6_m	Leishmania major resistance QTL 6 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9175833
1558866	Lmrq6_m	Leishmania major resistance QTL 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9175833
1558867	Gnf3_m	growth and fatness 3 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15769905
1558867	Gnf3_m	growth and fatness 3 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15769905
1558867	Gnf3_m	growth and fatness 3 (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15769905
1558868	Ses9_m	salmonella enteritidis susceptibility 9 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15973461
1558868	Ses9_m	salmonella enteritidis susceptibility 9 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15973461
1558869	Abfp5_m	abdominal fat percentage 5 (mouse)	qtl	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1558869	Abfp5_m	abdominal fat percentage 5 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558870	Eae36_m	experimental allergic encephalomyelitis susceptibility 36 (mouse)	qtl	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20111116	MGI			PMID:15917267
1558870	Eae36_m	experimental allergic encephalomyelitis susceptibility 36 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15917267
1558871	Mfiq3_m	M16 feed intake QTL 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558871	Mfiq3_m	M16 feed intake QTL 3 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558872	Ibdq1_m	inflammatory bowel disease QTL 1 (mouse)	qtl	MP:0002581	abnormal ileum morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12891551
1558872	Ibdq1_m	inflammatory bowel disease QTL 1 (mouse)	qtl	MP:0005381	digestive/alimentary phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12891551
1558872	Ibdq1_m	inflammatory bowel disease QTL 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12891551
1558872	Ibdq1_m	inflammatory bowel disease QTL 1 (mouse)	qtl	MP:0009482	ileum inflammation		IAGP		N	RGD:5509061	20111116	MGI			PMID:12891551
1558873	Hrtfm7_m	heart failure modifier 7 (mouse)	qtl	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20111116	MGI			PMID:16075368
1558873	Hrtfm7_m	heart failure modifier 7 (mouse)	qtl	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20111116	MGI			PMID:16075368
1558873	Hrtfm7_m	heart failure modifier 7 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16075368
1558873	Hrtfm7_m	heart failure modifier 7 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16075368
1558873	Hrtfm7_m	heart failure modifier 7 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16075368
1558875	Eae31_m	experimental allergic encephalomyelitis susceptibility 31 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15917267
1558875	Eae31_m	experimental allergic encephalomyelitis susceptibility 31 (mouse)	qtl	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20111116	MGI			PMID:15917267
1558876	W3q14_m	weight 3 weeks QTL 14 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558876	W3q14_m	weight 3 weeks QTL 14 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558877	W10q1_m	weight 10 weeks QTL 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558877	W10q1_m	weight 10 weeks QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558880	Scc12_m	colon tumor susceptibility 12 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14562056
1558880	Scc12_m	colon tumor susceptibility 12 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:14562056
1558881	Ses7_m	salmonella enteritidis susceptibility 7 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15973461
1558881	Ses7_m	salmonella enteritidis susceptibility 7 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15973461
1558882	Tsvw1_m	testis and seminal vesicles weight 1 (mouse)	qtl	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11333241
1558882	Tsvw1_m	testis and seminal vesicles weight 1 (mouse)	qtl	MP:0004909	increased seminal vesicle weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11333241
1558882	Tsvw1_m	testis and seminal vesicles weight 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11333241
1558882	Tsvw1_m	testis and seminal vesicles weight 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11333241
1558883	Abfp4_m	abdominal fat percentage 4 (mouse)	qtl	MP:0000010	abnormal abdominal fat pad morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1558883	Abfp4_m	abdominal fat percentage 4 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558884	Nsila7_m	novelty/stress induced locomotor activation 7 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1558884	Nsila7_m	novelty/stress induced locomotor activation 7 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1558889	Mfiq4_m	M16 feed intake QTL 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558889	Mfiq4_m	M16 feed intake QTL 4 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558890	Lith18_m	lithogenic gene 18 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:15834632
1558890	Lith18_m	lithogenic gene 18 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15834632
1558892	Ptnu1_m	proteinuria 1 (mouse)	qtl	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15965785
1558892	Ptnu1_m	proteinuria 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15965785
1558892	Ptnu1_m	proteinuria 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15965785
1558893	Spir1_m	Streptococcus pneumoniae infection resistance 1 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12925893
1558893	Spir1_m	Streptococcus pneumoniae infection resistance 1 (mouse)	qtl	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:12925893
1558893	Spir1_m	Streptococcus pneumoniae infection resistance 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12925893
1558894	Tlag1_m	T lymphoma attenuation gene 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:2552132
1558894	Tlag1_m	T lymphoma attenuation gene 1 (mouse)	qtl	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20111215	MGI			PMID:11813303
1558894	Tlag1_m	T lymphoma attenuation gene 1 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:2552132
1558894	Tlag1_m	T lymphoma attenuation gene 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:2552132
1558894	Tlag1_m	T lymphoma attenuation gene 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:2552132
1558895	Nsila6_m	novelty/stress induced locomotor activation 6 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1558895	Nsila6_m	novelty/stress induced locomotor activation 6 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1558896	Motp1_m	modifier of Trp53 1 (mouse)	qtl	MP:0004179	transmission ratio distortion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181534
1558896	Motp1_m	modifier of Trp53 1 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181534
1558896	Motp1_m	modifier of Trp53 1 (mouse)	qtl	MP:0010768	mortality/aging		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15181534
1558896	Motp1_m	modifier of Trp53 1 (mouse)	qtl	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20111116	MGI			PMID:15181534
1558897	Bodw1_m	body weight 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1558897	Bodw1_m	body weight 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558898	Hpi1_m	hapatic PMN infiltration 1 (mouse)	qtl	MP:0001845	abnormal inflammatory response		IAGP		N	RGD:5509061	20111116	MGI			PMID:11053246
1558898	Hpi1_m	hapatic PMN infiltration 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11053246
1558899	Egq1_m	early growth QTL 1 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558899	Egq1_m	early growth QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558901	Skmw8_m	skeletal muscle weight  8 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15687484
1558901	Skmw8_m	skeletal muscle weight  8 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15687484
1558901	Skmw8_m	skeletal muscle weight  8 (mouse)	qtl	MP:0009423	increased extensor digitorum longus weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1558901	Skmw8_m	skeletal muscle weight  8 (mouse)	qtl	MP:0009427	increased tibialis anterior weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558901	Skmw8_m	skeletal muscle weight  8 (mouse)	qtl	MP:0009427	increased tibialis anterior weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1558902	Mnek1a_m	modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse)	qtl	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20111116	MGI			PMID:10366444
1558902	Mnek1a_m	modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:10366444
1558902	Mnek1a_m	modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10366444
1558902	Mnek1a_m	modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:10366444
1558902	Mnek1a_m	modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10366444
1558903	Salpa2_m	serum alkaline phosphatase activity 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15542033
1558903	Salpa2_m	serum alkaline phosphatase activity 2 (mouse)	qtl	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20120209	MGI			PMID:15542033
1558904	Nsila9_m	novelty/stress induced locomotor activation 9 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1558904	Nsila9_m	novelty/stress induced locomotor activation 9 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1558905	Gct7_m	granulosa cell tumorigenesis 7 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15735010
1558905	Gct7_m	granulosa cell tumorigenesis 7 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15735010
1558905	Gct7_m	granulosa cell tumorigenesis 7 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15735010
1558905	Gct7_m	granulosa cell tumorigenesis 7 (mouse)	qtl	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20131227	MGI			PMID:15735010
1558907	Spnw1_m	spleen weight 1 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1558907	Spnw1_m	spleen weight 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:16151693
1558907	Spnw1_m	spleen weight 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558907	Spnw1_m	spleen weight 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558908	W10q12_m	weight 10 weeks QTL 12 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558908	W10q12_m	weight 10 weeks QTL 12 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558912	Marq4_m	methamphetamine response QTL 4 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104378
1558912	Marq4_m	methamphetamine response QTL 4 (mouse)	qtl	MP:0009749	enhanced behavioral response to addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104378
1558913	Afw7_m	abdominal fat weight QTL 7 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11116089|PMID:9725853
1558914	Artmd2_m	arthropathy in MRL and DBA/1 mice 2 (mouse)	qtl	MP:0002936	joint swelling		IAGP		N	RGD:5509061	20111116	MGI			PMID:15751084
1558914	Artmd2_m	arthropathy in MRL and DBA/1 mice 2 (mouse)	qtl	MP:0003189	fused joints		IAGP		N	RGD:5509061	20111116	MGI			PMID:15751084
1558914	Artmd2_m	arthropathy in MRL and DBA/1 mice 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15751084
1558914	Artmd2_m	arthropathy in MRL and DBA/1 mice 2 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15751084
1558915	W3q1_m	weight 3 weeks QTL 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558915	W3q1_m	weight 3 weeks QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558916	Egq5_m	early growth QTL 5 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558916	Egq5_m	early growth QTL 5 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558917	Gct8_m	granulosa cell tumorigenesis 8 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15735010
1558917	Gct8_m	granulosa cell tumorigenesis 8 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15735010
1558917	Gct8_m	granulosa cell tumorigenesis 8 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15735010
1558917	Gct8_m	granulosa cell tumorigenesis 8 (mouse)	qtl	MP:0012411	increased granulosa cell tumor incidence		IAGP		N	RGD:5509061	20131227	MGI			PMID:15735010
1558918	Manln16_m	mandible length 16 (mouse)	qtl	MP:0004593	long mandible		IAGP		N	RGD:5509061	20111116	MGI			PMID:15384169
1558918	Manln16_m	mandible length 16 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20250815	MGI		Created by mouse qtl pipeline	PMID:15384169
1558918	Manln16_m	mandible length 16 (mouse)	qtl	MP:0005382	craniofacial phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1558918	Manln16_m	mandible length 16 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15384169
1558920	Trglyd_m	triglycerides (mouse)	qtl	MP:0005317	increased triglyceride level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15524312
1558920	Trglyd_m	triglycerides (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15524312
1558921	Ethm2_m	ethanol induced thermoregulation 2 (mouse)	qtl	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11773602
1558921	Ethm2_m	ethanol induced thermoregulation 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11773602
1558925	Hivan1_m	HIV-associated nephropathy 1 (mouse)	qtl	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:14983036
1558925	Hivan1_m	HIV-associated nephropathy 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14983036
1558927	Mfi5q1_m	M16 feed intake at 5 weeks QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558927	Mfi5q1_m	M16 feed intake at 5 weeks QTL 1 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558928	Mord2_m	modifier of retinal degeneration 2 (mouse)	qtl	MP:0003455	decreased susceptibility to induced retina damage		IAGP		N	RGD:5509061	20111116	MGI			PMID:15947737
1558928	Mord2_m	modifier of retinal degeneration 2 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15947737
1558929	Gsi1_m	glomerulsclerosis index 1 (mouse)	qtl	MP:0005264	glomerulosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:16093645
1558929	Gsi1_m	glomerulsclerosis index 1 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16093645
1558930	Knyw4_m	kidney weight 4 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1558930	Knyw4_m	kidney weight 4 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558930	Knyw4_m	kidney weight 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:16151693
1558931	Scpro4_m	Stem cell proliferation 4 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11698278
1558931	Scpro4_m	Stem cell proliferation 4 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11698278
1558933	Ses1b_m	salmonella enteritidis susceptibility 1b (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15973461
1558933	Ses1b_m	salmonella enteritidis susceptibility 1b (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15973461
1558934	Cplaq12_m	circadian period of locomotor activity 12 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14667146
1558934	Cplaq12_m	circadian period of locomotor activity 12 (mouse)	qtl	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:14667146
1558936	Eae38_m	experimental allergic encephalomyelitis susceptibility 38 (mouse)	qtl	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20111116	MGI			PMID:15917267
1558936	Eae38_m	experimental allergic encephalomyelitis susceptibility 38 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15917267
1558938	Ethm1_m	ethanol induced thermoregulation 1 (mouse)	qtl	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11773602
1558938	Ethm1_m	ethanol induced thermoregulation 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11773602
1558939	Gnf1_m	growth and fatness 1 (mouse)	qtl	MP:0000063	decreased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:15769905
1558939	Gnf1_m	growth and fatness 1 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15769905
1558939	Gnf1_m	growth and fatness 1 (mouse)	qtl	MP:0002089	abnormal postnatal growth/weight/body size		IAGP		N	RGD:5509061	20111116	MGI			PMID:15769905
1558939	Gnf1_m	growth and fatness 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15769905
1558939	Gnf1_m	growth and fatness 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15769905
1558939	Gnf1_m	growth and fatness 1 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15769905
1558939	Gnf1_m	growth and fatness 1 (mouse)	qtl	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20111116	MGI			PMID:15769905
1558940	Imebt1_m	imprinting effect on body traits 1 (mouse)	qtl	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15761081
1558940	Imebt1_m	imprinting effect on body traits 1 (mouse)	qtl	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20111116	MGI			PMID:15761081
1558940	Imebt1_m	imprinting effect on body traits 1 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15761081
1558940	Imebt1_m	imprinting effect on body traits 1 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15761081
1558940	Imebt1_m	imprinting effect on body traits 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15761081
1558940	Imebt1_m	imprinting effect on body traits 1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15761081
1558940	Imebt1_m	imprinting effect on body traits 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15761081
1558940	Imebt1_m	imprinting effect on body traits 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15761081
1558942	Lith16_m	lithogenic gene 16 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151694
1558942	Lith16_m	lithogenic gene 16 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151694
1558943	Scpro6_m	Stem cell proliferation 6 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11698278
1558943	Scpro6_m	Stem cell proliferation 6 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:17220891
1558943	Scpro6_m	Stem cell proliferation 6 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11698278
1558945	Orgwq8_m	organ weight QTL 8 (mouse)	qtl	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1558945	Orgwq8_m	organ weight QTL 8 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1558945	Orgwq8_m	organ weight QTL 8 (mouse)	qtl	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:12118102
1558945	Orgwq8_m	organ weight QTL 8 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1558945	Orgwq8_m	organ weight QTL 8 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1558945	Orgwq8_m	organ weight QTL 8 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:12118102
1558945	Orgwq8_m	organ weight QTL 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1558945	Orgwq8_m	organ weight QTL 8 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12118102
1558946	Scpro11_m	Stem cell proliferation 11 (mouse)	qtl	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11698278
1558946	Scpro11_m	Stem cell proliferation 11 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11698278
1558947	Ptnu5_m	proteinuria 5 (mouse)	qtl	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15965785
1558947	Ptnu5_m	proteinuria 5 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15965785
1558947	Ptnu5_m	proteinuria 5 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15965785
1558948	Ath8_m	atherosclerosis 8 (mouse)	qtl	MP:0005338	atherosclerotic lesions		IAGP		N	RGD:5509061	20111116	MGI			PMID:15530921
1558948	Ath8_m	atherosclerosis 8 (mouse)	qtl	MP:0005339	increased susceptibility to atherosclerosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15530921
1558948	Ath8_m	atherosclerosis 8 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:17916774|PMID:15530921
1558948	Ath8_m	atherosclerosis 8 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20151218	MGI		Created by mouse qtl pipeline	PMID:15530921
1558950	Nsila3_m	novelty/stress induced locomotor activation 3 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1558950	Nsila3_m	novelty/stress induced locomotor activation 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1558951	mdlk1_m	modifier of Dlk1 (mouse)	qtl	MP:0003787	abnormal imprinting		IAGP		N	RGD:5509061	20111116	MGI			PMID:15859358
1558951	mdlk1_m	modifier of Dlk1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15859358
1558951	mdlk1_m	modifier of Dlk1 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15859358
1558954	Hypism_m	hyperinsulinemia (mouse)	qtl	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15514201
1558954	Hypism_m	hyperinsulinemia (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15514201
1558956	Lith19_m	lithogenic gene 19 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:15834632
1558956	Lith19_m	lithogenic gene 19 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15834632
1558958	Tesw2_m	testis weight 2 (mouse)	qtl	MP:0004851	increased testis weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:11333241
1558958	Tesw2_m	testis weight 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11333241
1558958	Tesw2_m	testis weight 2 (mouse)	qtl	MP:0005389	reproductive system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11333241
1558959	Eamcd2_m	experimental autoimmune myocarditis 2 (mouse)	qtl	MP:0001856	myocarditis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15699148
1558959	Eamcd2_m	experimental autoimmune myocarditis 2 (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15699148
1558959	Eamcd2_m	experimental autoimmune myocarditis 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15699148
1558960	Mfe5q1_m	M16 feed efficiency at 5 weeks QTL 1 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1558960	Mfe5q1_m	M16 feed efficiency at 5 weeks QTL 1 (mouse)	qtl	MP:0005449	abnormal food intake		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1558961	Nidd1_m	non-insulin-dependent diabetes mellitus 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:9703330
1558961	Nidd1_m	non-insulin-dependent diabetes mellitus 1 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:9703330
1558961	Nidd1_m	non-insulin-dependent diabetes mellitus 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9703330
1558961	Nidd1_m	non-insulin-dependent diabetes mellitus 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9703330
1558962	Cms1_m	resistance to Coccidioides immitis 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:10338499
1558962	Cms1_m	resistance to Coccidioides immitis 1 (mouse)	qtl	MP:0005398	decreased susceptibility to fungal infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:10338499
1558965	Hcs3_m	hepatocarcinogenesis susceptibility 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8417808
1558965	Hcs3_m	hepatocarcinogenesis susceptibility 3 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:8417808
1558965	Hcs3_m	hepatocarcinogenesis susceptibility 3 (mouse)	qtl	MP:0010264	increased hepatoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:8417808
1558966	W10q9_m	weight 10 weeks QTL 9 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558966	W10q9_m	weight 10 weeks QTL 9 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558967	Scc15_m	colon tumor susceptibility 15 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14562056
1558967	Scc15_m	colon tumor susceptibility 15 (mouse)	qtl	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:14562056
1558968	Tbdr1_m	body temperature response to dietary restriction, QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14999024
1558968	Tbdr1_m	body temperature response to dietary restriction, QTL 1 (mouse)	qtl	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20111116	MGI			PMID:14999024
1558969	W6q11_m	weight 6 weeks QTL 11 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558969	W6q11_m	weight 6 weeks QTL 11 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558971	Imebt2_m	imprinting effect on body traits 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15761081
1558971	Imebt2_m	imprinting effect on body traits 2 (mouse)	qtl	MP:0002981	increased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15761081
1558971	Imebt2_m	imprinting effect on body traits 2 (mouse)	qtl	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20111116	MGI			PMID:15761081
1558971	Imebt2_m	imprinting effect on body traits 2 (mouse)	qtl	MP:0003917	increased kidney weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15761081
1558971	Imebt2_m	imprinting effect on body traits 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15761081
1558971	Imebt2_m	imprinting effect on body traits 2 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15761081
1558971	Imebt2_m	imprinting effect on body traits 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15761081
1558971	Imebt2_m	imprinting effect on body traits 2 (mouse)	qtl	MP:0005384	cellular phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15761081
1558972	Erars1_m	erosive arthritis susceptibility 1 (mouse)	qtl	MP:0002461	increased immunoglobulin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15683449
1558972	Erars1_m	erosive arthritis susceptibility 1 (mouse)	qtl	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15683449
1558972	Erars1_m	erosive arthritis susceptibility 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15683449
1558972	Erars1_m	erosive arthritis susceptibility 1 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20131213	MGI		Created by mouse qtl pipeline	PMID:15683449
1558974	Vacq6_m	voluntary alcohol consumption QTL 6 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558974	Vacq6_m	voluntary alcohol consumption QTL 6 (mouse)	qtl	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1558974	Vacq6_m	voluntary alcohol consumption QTL 6 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104380
1558975	Marq3_m	methamphetamine response QTL 3 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104378
1558975	Marq3_m	methamphetamine response QTL 3 (mouse)	qtl	MP:0009750	impaired behavioral response to addictive substance		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104378
1558976	Ptnu4_m	proteinuria 4 (mouse)	qtl	MP:0002962	increased urine protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15965785
1558976	Ptnu4_m	proteinuria 4 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15965785
1558976	Ptnu4_m	proteinuria 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15965785
1558977	Skmw10_m	skeletal muscle weight  10 (mouse)	qtl	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558977	Skmw10_m	skeletal muscle weight  10 (mouse)	qtl	MP:0003082	abnormal gastrocnemius morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1558977	Skmw10_m	skeletal muscle weight  10 (mouse)	qtl	MP:0003397	increased muscle weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1558977	Skmw10_m	skeletal muscle weight  10 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15687484
1558977	Skmw10_m	skeletal muscle weight  10 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15687484
1558977	Skmw10_m	skeletal muscle weight  10 (mouse)	qtl	MP:0009421	increased gastrocnemius weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558978	Cplaq10_m	circadian period of locomotor activity 10 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14667146
1558978	Cplaq10_m	circadian period of locomotor activity 10 (mouse)	qtl	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:14667146
1558979	Ofact_m	open field activity (mouse)	qtl	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20111116	MGI			PMID:11544198
1558979	Ofact_m	open field activity (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11544198
1558980	Idd15_m	insulin dependent diabetes susceptibility 15 (mouse)	qtl	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:7556956
1558980	Idd15_m	insulin dependent diabetes susceptibility 15 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:7556956
1558982	Eae37_m	experimental allergic encephalomyelitis susceptibility 37 (mouse)	qtl	MP:0005350	increased susceptibility to autoimmune disorder		IAGP		N	RGD:5509061	20111116	MGI			PMID:15917267
1558982	Eae37_m	experimental allergic encephalomyelitis susceptibility 37 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15917267
1558984	Cplaq9_m	circadian period of locomotor activity 9 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:14667146
1558984	Cplaq9_m	circadian period of locomotor activity 9 (mouse)	qtl	MP:0020470	shortened circadian behavior period		IAGP		N	RGD:5509061	20171012	MGI			PMID:14667146
1558985	Eae32_m	experimental allergic encephalomyelitis susceptibility 32 (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15917267
1558985	Eae32_m	experimental allergic encephalomyelitis susceptibility 32 (mouse)	qtl	MP:0005403	abnormal nerve conduction		IAGP		N	RGD:5509061	20111116	MGI			PMID:15917267
1558987	Psl4_m	promotion susceptibility QTL 4 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12782578
1558987	Psl4_m	promotion susceptibility QTL 4 (mouse)	qtl	MP:0010300	increased skin tumor incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:12782578
1558987	Psl4_m	promotion susceptibility QTL 4 (mouse)	qtl	MP:0010771	integument phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12782578
1558988	Bodw2_m	body weight 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1558988	Bodw2_m	body weight 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1558989	Gnf4_m	growth and fatness 4 (mouse)	qtl	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15769905
1558989	Gnf4_m	growth and fatness 4 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15769905
1558990	Skmw9_m	skeletal muscle weight 9 (mouse)	qtl	MP:0005369	muscle phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15687484
1558990	Skmw9_m	skeletal muscle weight 9 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:15687484
1558990	Skmw9_m	skeletal muscle weight 9 (mouse)	qtl	MP:0009421	increased gastrocnemius weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15687484
1558990	Skmw9_m	skeletal muscle weight 9 (mouse)	qtl	MP:0009421	increased gastrocnemius weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16783642
1558991	Tailq4_m	tail length QTL 4 (mouse)	qtl	MP:0002758	long tail		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558991	Tailq4_m	tail length QTL 4 (mouse)	qtl	MP:0005371	limbs/digits/tail phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558992	Ses8_m	salmonella enteritidis susceptibility 8 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15973461
1558992	Ses8_m	salmonella enteritidis susceptibility 8 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15973461
1558993	Tdmq1_m	type 2 diabetes modifying QTL 1 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15820311
1558993	Tdmq1_m	type 2 diabetes modifying QTL 1 (mouse)	qtl	MP:0005375	adipose tissue phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15820311
1558993	Tdmq1_m	type 2 diabetes modifying QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15820311
1558993	Tdmq1_m	type 2 diabetes modifying QTL 1 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15820311
1558993	Tdmq1_m	type 2 diabetes modifying QTL 1 (mouse)	qtl	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15820311
1558993	Tdmq1_m	type 2 diabetes modifying QTL 1 (mouse)	qtl	MP:0009300	increased parametrial fat pad weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15820311
1558994	W6q2_m	weight 6 weeks QTL 2 (mouse)	qtl	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558994	W6q2_m	weight 6 weeks QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558995	Tsiq3_m	T-cell secretion of IL-4 QTL 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15815685
1558995	Tsiq3_m	T-cell secretion of IL-4 QTL 3 (mouse)	qtl	MP:0008699	increased interleukin-4 secretion		IAGP		N	RGD:5509061	20111116	MGI			PMID:15815685
1558996	Bomd7_m	bone mineral density 7 (mouse)	qtl	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20111116	MGI			PMID:11697791
1558996	Bomd7_m	bone mineral density 7 (mouse)	qtl	MP:0005390	skeleton phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11697791
1558997	Lgq2_m	late growth QTL 2 (mouse)	qtl	MP:0002865	increased growth rate		IAGP		N	RGD:5509061	20111116	MGI			PMID:15058380
1558997	Lgq2_m	late growth QTL 2 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15058380
1558998	Ses5_m	salmonella enteritidis susceptibility 5 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15973461
1558998	Ses5_m	salmonella enteritidis susceptibility 5 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15973461
1558999	Ethm4_m	ethanol induced thermoregulation 4 (mouse)	qtl	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20111116	MGI			PMID:11773602
1558999	Ethm4_m	ethanol induced thermoregulation 4 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11773602
1559000	Ossc1_m	osteosarcoma susceptibility 1 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11893245
1559000	Ossc1_m	osteosarcoma susceptibility 1 (mouse)	qtl	MP:0002032	increased sarcoma incidence		IAGP		N	RGD:5509061	20111116	MGI			PMID:11893245
1559001	Eae33_m	experimental allergic encephalomyelitis susceptibility 33 (mouse)	qtl	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15917267
1559001	Eae33_m	experimental allergic encephalomyelitis susceptibility 33 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15917267
1559002	Lmrq4_m	Leishmania major resistance QTL 4 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9175833
1559002	Lmrq4_m	Leishmania major resistance QTL 4 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9175833
1559004	Mglcq1_m	M16 glucose QTL 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1559004	Mglcq1_m	M16 glucose QTL 1 (mouse)	qtl	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1559006	Ses6_m	salmonella enteritidis susceptibility 6 (mouse)	qtl	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:15973461
1559006	Ses6_m	salmonella enteritidis susceptibility 6 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15973461
1559008	Lith22_m	lithogenic gene 22 (mouse)	qtl	MP:0002830	gallstones		IAGP		N	RGD:5509061	20111116	MGI			PMID:15834632
1559008	Lith22_m	lithogenic gene 22 (mouse)	qtl	MP:0005370	liver/biliary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15834632
1559009	Vacq7_m	voluntary alcohol consumption QTL 7 (mouse)	qtl	MP:0001987	alcohol preference		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1559009	Vacq7_m	voluntary alcohol consumption QTL 7 (mouse)	qtl	MP:0003545	increased alcohol consumption		IAGP		N	RGD:5509061	20111116	MGI			PMID:16104380
1559009	Vacq7_m	voluntary alcohol consumption QTL 7 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16104380
1559010	Nsila8_m	novelty/stress induced locomotor activation 8 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1559010	Nsila8_m	novelty/stress induced locomotor activation 8 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1559012	Nsila10_m	novelty/stress induced locomotor activation 10 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1559012	Nsila10_m	novelty/stress induced locomotor activation 10 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1559013	Htas2_m	hypothermia due to alcohol sensitivity 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:8169823
1559013	Htas2_m	hypothermia due to alcohol sensitivity 2 (mouse)	qtl	MP:0005443	abnormal ethanol metabolism		IAGP		N	RGD:5509061	20111116	MGI			PMID:8169823
1559013	Htas2_m	hypothermia due to alcohol sensitivity 2 (mouse)	qtl	MP:0005534	decreased body temperature		IAGP		N	RGD:5509061	20111116	MGI			PMID:8169823
1559014	Agnm3_m	autoimmune glomerulonephritis in MRL 3 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15832294
1559014	Agnm3_m	autoimmune glomerulonephritis in MRL 3 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:15832294
1559014	Agnm3_m	autoimmune glomerulonephritis in MRL 3 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15832294
1559014	Agnm3_m	autoimmune glomerulonephritis in MRL 3 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15832294
1559015	Bodw4_m	body weight 4 (mouse)	qtl	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20111116	MGI			PMID:16151693
1559015	Bodw4_m	body weight 4 (mouse)	qtl	MP:0005378	growth/size/body region phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16151693
1559016	Drsi_m	DCC-related Spp1 induction (mouse)	qtl	MP:0002837	dystrophic cardiac calcinosis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15039225
1559016	Drsi_m	DCC-related Spp1 induction (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15039225
1559016	Drsi_m	DCC-related Spp1 induction (mouse)	qtl	MP:0005385	cardiovascular system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15039225
1559016	Drsi_m	DCC-related Spp1 induction (mouse)	qtl	MP:0005568	increased circulating total protein level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15039225
1559017	Lmrq1_m	Leishmania major resistance QTL 1 (mouse)	qtl	MP:0005026	decreased susceptibility to parasitic infection		IAGP		N	RGD:5509061	20111116	MGI			PMID:9175833
1559017	Lmrq1_m	Leishmania major resistance QTL 1 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:9175833
1559018	Mord3_m	modifier of retinal degeneration 3 (mouse)	qtl	MP:0003455	decreased susceptibility to induced retina damage		IAGP		N	RGD:5509061	20111116	MGI			PMID:15947737
1559018	Mord3_m	modifier of retinal degeneration 3 (mouse)	qtl	MP:0005391	vision/eye phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15947737
1559019	Mlepq2_m	M16 leptin QTL 2 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15944354
1559019	Mlepq2_m	M16 leptin QTL 2 (mouse)	qtl	MP:0005669	increased circulating leptin level		IAGP		N	RGD:5509061	20111116	MGI			PMID:15944354
1559020	Mmtp3_m	modifier of mammary tumor progression 3 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15859357
1559020	Mmtp3_m	modifier of mammary tumor progression 3 (mouse)	qtl	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20111116	MGI			PMID:15859357
1559021	Tlag2_m	T lymphoma attenuation gene 2 (mouse)	qtl	MP:0002006	neoplasm		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:11813303
1559021	Tlag2_m	T lymphoma attenuation gene 2 (mouse)	qtl	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20111215	MGI			PMID:11813303
1559021	Tlag2_m	T lymphoma attenuation gene 2 (mouse)	qtl	MP:0005379	endocrine/exocrine gland phenotype		IEA		N	RGD:704405	20231117	MGI		Created by mouse qtl pipeline	PMID:11813303
1559021	Tlag2_m	T lymphoma attenuation gene 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:11813303
1559021	Tlag2_m	T lymphoma attenuation gene 2 (mouse)	qtl	MP:0005397	hematopoietic system phenotype		IEA		N	RGD:704405	20241101	MGI		Created by mouse qtl pipeline	PMID:11813303
1559023	Gbrln_m	granular brain lesions (mouse)	qtl	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20111116	MGI			PMID:12828934
1559023	Gbrln_m	granular brain lesions (mouse)	qtl	MP:0003631	nervous system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:12828934
1559024	Zit1_m	zinc induced tolerance 1 (mouse)	qtl	MP:0005376	homeostasis/metabolism phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:16026622
1559024	Zit1_m	zinc induced tolerance 1 (mouse)	qtl	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20111116	MGI			PMID:16026622
1559025	Agnm2_m	autoimmune glomerulonephritis in MRL 2 (mouse)	qtl	MP:0002743	glomerulonephritis		IAGP		N	RGD:5509061	20111116	MGI			PMID:15832294
1559025	Agnm2_m	autoimmune glomerulonephritis in MRL 2 (mouse)	qtl	MP:0004801	increased susceptibility to systemic lupus erythematosus		IAGP		N	RGD:5509061	20111116	MGI			PMID:15832294
1559025	Agnm2_m	autoimmune glomerulonephritis in MRL 2 (mouse)	qtl	MP:0005367	renal/urinary system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15832294
1559025	Agnm2_m	autoimmune glomerulonephritis in MRL 2 (mouse)	qtl	MP:0005387	immune system phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15832294
1559026	Nsila2_m	novelty/stress induced locomotor activation 2 (mouse)	qtl	MP:0001364	decreased anxiety-related response		IAGP		N	RGD:5509061	20111116	MGI			PMID:15904718
1559026	Nsila2_m	novelty/stress induced locomotor activation 2 (mouse)	qtl	MP:0005386	behavior/neurological phenotype		IEA		N	RGD:704405	20120116	MGI		Created by mouse qtl pipeline	PMID:15904718
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0000755	hindlimb paralysis		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0000756	forelimb paralysis		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0001053	abnormal neuromuscular synapse morphology		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0001107	decreased Schwann cell number		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0001575	cyanosis		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0002914	abnormal endplate potential		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0003651	abnormal axon extension		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0005281	increased fatty acids level		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0005365	abnormal bile salt homeostasis		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0009450	abnormal axon fasciculation		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0011090	perinatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0012216	decreased plasmalogen level		IAGP		N	RGD:5509061	20150625	MGI			PMID:25176044
1607093	Pex10	peroxisomal biogenesis factor 10	gene	MP:0031494	abnormal prenatal movement		IAGP		N	RGD:5509061	20230810	MGI			PMID:25176044
1607095	Snord115	small nucleolar RNA, C/D Box 115 cluster	gene	MP:0000005	increased brown adipose tissue amount		IAGP		N	RGD:5509061	20210617	MGI			PMID:33016258
1607095	Snord115	small nucleolar RNA, C/D Box 115 cluster	gene	MP:0003122	maternal imprinting		IAGP		N	RGD:5509061	20210617	MGI			PMID:33016258
1607095	Snord115	small nucleolar RNA, C/D Box 115 cluster	gene	MP:0003360	abnormal depression-related behavior		IAGP		N	RGD:5509061	20210617	MGI			PMID:33016258
1607119	Dgat2l6	diacylglycerol O-acyltransferase 2-like 6	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20210128	MGI			
1607119	Dgat2l6	diacylglycerol O-acyltransferase 2-like 6	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20181227	MGI			
1607119	Dgat2l6	diacylglycerol O-acyltransferase 2-like 6	gene	MP:0001284	absent vibrissae		IEA		N	RGD:5509061	20181227	MGI			
1607119	Dgat2l6	diacylglycerol O-acyltransferase 2-like 6	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20181227	MGI			
1607119	Dgat2l6	diacylglycerol O-acyltransferase 2-like 6	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1607119	Dgat2l6	diacylglycerol O-acyltransferase 2-like 6	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20231207	MGI			
1607175	Eid2b	EP300 interacting inhibitor of differentiation 2B	gene	MP:0000062	increased bone mineral density		IEA		N	RGD:5509061	20220811	MGI			
1607175	Eid2b	EP300 interacting inhibitor of differentiation 2B	gene	MP:0000195	decreased circulating calcium level		IEA		N	RGD:5509061	20230601	MGI			
1607175	Eid2b	EP300 interacting inhibitor of differentiation 2B	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1607175	Eid2b	EP300 interacting inhibitor of differentiation 2B	gene	MP:0002591	decreased mean corpuscular volume		IEA		N	RGD:5509061	20220811	MGI			
1607175	Eid2b	EP300 interacting inhibitor of differentiation 2B	gene	MP:0005559	increased circulating glucose level		IEA		N	RGD:5509061	20230601	MGI			
1607175	Eid2b	EP300 interacting inhibitor of differentiation 2B	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20220519	MGI			
1607175	Eid2b	EP300 interacting inhibitor of differentiation 2B	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20220811	MGI			
1607175	Eid2b	EP300 interacting inhibitor of differentiation 2B	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20220519	MGI			
1607290	Misfadt	mitochondrial sheath formation associated divergent transcript	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20220901	MGI			PMID:31956907
1607350	Majin	membrane anchored junction protein	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20211021	MGI			PMID:34326397
1607350	Majin	membrane anchored junction protein	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20211021	MGI			PMID:34326397
1607350	Majin	membrane anchored junction protein	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20211021	MGI			PMID:34326397
1607350	Majin	membrane anchored junction protein	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20211021	MGI			PMID:34326397
1607365	Prr30	proline rich 30	gene	MP:0000221	decreased leukocyte cell number		IEA		N	RGD:5509061	20241121	MGI			
1607447	3930402G23Rik	RIKEN cDNA 3930402G23 gene	gene	MP:0000598	abnormal liver morphology		IAGP		N	RGD:5509061	20240509	MGI			PMID:35917881
1607447	3930402G23Rik	RIKEN cDNA 3930402G23 gene	gene	MP:0009355	increased liver triglyceride level		IAGP		N	RGD:5509061	20240509	MGI			PMID:35917881
1607447	3930402G23Rik	RIKEN cDNA 3930402G23 gene	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20240509	MGI			PMID:35917881
1607447	3930402G23Rik	RIKEN cDNA 3930402G23 gene	gene	MP:0010359	increased liver free fatty acids level		IAGP		N	RGD:5509061	20240509	MGI			PMID:35917881
1607447	3930402G23Rik	RIKEN cDNA 3930402G23 gene	gene	MP:0031265	increased susceptibility to hepatic steatosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:35917881
1607458	Foxd3os	Forkhead box D3 opposite strand	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000074	abnormal neurocranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000107	abnormal frontal bone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000137	abnormal vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000163	abnormal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000433	microcephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000454	abnormal jaw morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000547	short limbs		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000592	short tail		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000603	pale liver		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0000607	abnormal hepatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0001258	decreased body length		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0001698	decreased embryo size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831459
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0002084	abnormal developmental patterning		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831459
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0002109	abnormal limb morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:9159106
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0002896	abnormal bone mineralization		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0003049	abnormal lumbar vertebrae morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0003103	liver degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0003120	abnormal tracheal cartilage morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0003662	abnormal long bone epiphyseal plate proliferative zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0003935	abnormal craniofacial development		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0005352	small cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0006042	increased apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0006398	increased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0008412	increased cellular sensitivity to oxidative stress		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0010883	trachea stenosis		IAGP		N	RGD:5509061	20150212	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0011084	lethality at weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18039655
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:12588969
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:9159106
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0011097	embryonic lethality between somite formation and embryo turning, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:15831459
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0013753	tracheomalacia		IAGP		N	RGD:5509061	20150416	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0030262	frontal bossing		IAGP		N	RGD:5509061	20171026	MGI			PMID:19696890
1607539	n-TUtca2	nuclear encoded tRNA selenocysteine 2 (anticodon TCA)	gene	MP:0030297	outer ear hypoplasia		IAGP		N	RGD:5509061	20171102	MGI			PMID:19696890
1607556	Mir9-3	microRNA 9-3	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0004081	abnormal globus pallidus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0004172	abnormal subpallium development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0008031	decreased Cajal-Retzius cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0008440	abnormal subplate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607556	Mir9-3	microRNA 9-3	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0000776	abnormal inferior colliculus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0000787	abnormal telencephalon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0000790	abnormal cerebral cortex lamination		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0000792	abnormal cortical marginal zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0000818	abnormal amygdala morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0000934	abnormal telencephalon development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0002741	small olfactory bulb		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0004081	abnormal globus pallidus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0004101	abnormal brain interneuron morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0004172	abnormal subpallium development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0004277	abnormal lateral ganglionic eminence morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0005404	abnormal axon morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0008031	decreased Cajal-Retzius cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0008440	abnormal subplate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0008458	abnormal cortical ventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0008535	enlarged lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0008540	abnormal cerebral hemisphere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607557	Mir9-2	microRNA 9-2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21368052
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607562	Mir26a-2	microRNA 26a-2	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607563	Mir24-2	microRNA 24-2	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20210805	MGI			PMID:34107258
1607563	Mir24-2	microRNA 24-2	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20210805	MGI			PMID:34107258
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0000273	overriding aortic valve		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0001787	pericardial edema		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0003233	prolonged QT interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0004122	abnormal sinus arrhythmia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0004937	dilated heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0008725	increased heart atrium size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0010392	prolonged QRS complex duration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0010508	abnormal heart electrocardiography waveform feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0010577	abnormal heart right ventricle size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0010769	abnormal survival		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0011112	lethality during fetal growth through weaning, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:17397913
1607564	Mir1a-2	microRNA 1a-2	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20141003	MGI			PMID:24252873
1607565	Mir196a-2	microRNA 196a-2	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1607565	Mir196a-2	microRNA 196a-2	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1607565	Mir196a-2	microRNA 196a-2	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1607565	Mir196a-2	microRNA 196a-2	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1607565	Mir196a-2	microRNA 196a-2	gene	MP:0010113	abnormal sacrum morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0000266	abnormal heart morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0000274	enlarged heart		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0000278	abnormal myocardial fiber morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0000281	abnormal interventricular septum morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0001855	abnormal atrial thrombosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0002754	dilated heart right ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0002795	dilated cardiomyopathy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0003140	dilated heart atrium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0003920	abnormal heart right ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0005598	decreased heart ventricle muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0014343	abnormal myocardial fiber mitochondrial morphology		IAGP		N	RGD:5509061	20250911	MGI			PMID:19015276
1607569	Mir133a-2	microRNA 133a-2	gene	MP:0031633	decreased heart left ventricle muscle contractility		IAGP		N	RGD:5509061	20240704	MGI			PMID:19015276
1607570	Mir129-2	microRNA 129-2	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20240523	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20230601	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20230601	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0003961	decreased lean body mass		IEA		N	RGD:5509061	20230601	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20230601	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0004599	abnormal vertebral arch morphology		IEA		N	RGD:5509061	20230601	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0005293	impaired glucose tolerance		IEA		N	RGD:5509061	20230601	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0005567	decreased circulating total protein level		IEA		N	RGD:5509061	20230601	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20230601	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0010025	decreased total body fat amount		IEA		N	RGD:5509061	20250508	MGI			
1607570	Mir129-2	microRNA 129-2	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20230601	MGI			
1607572	Mir124a-3	microRNA 124a-3	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607572	Mir124a-3	microRNA 124a-3	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607572	Mir124a-3	microRNA 124a-3	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607572	Mir124a-3	microRNA 124a-3	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607573	Mir124a-2	microRNA 124a-2	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607573	Mir124a-2	microRNA 124a-2	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607573	Mir124a-2	microRNA 124a-2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607573	Mir124a-2	microRNA 124a-2	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607573	Mir124a-2	microRNA 124a-2	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607573	Mir124a-2	microRNA 124a-2	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1607598	Mir218-2	microRNA 218-2	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0001054	failure of neuromuscular synapse presynaptic differentiation		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607598	Mir218-2	microRNA 218-2	gene	MP:0020336	abnormal motor neuron dendrite morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1607601	Mir350	microRNA 350	gene	MP:0003921	abnormal heart left ventricle morphology		IEA		N	RGD:5509061	20231207	MGI			
1607619	Mir7-1	microRNA 7-1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190523	MGI			PMID:29887379
1607621	Mir375	microRNA 375	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0001426	polydipsia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0001762	polyuria		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0002078	abnormal glucose homeostasis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0002710	increased glucagon secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0002712	increased circulating glucagon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0003383	abnormal gluconeogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0005215	abnormal pancreatic islet morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0009176	increased pancreatic alpha cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607621	Mir375	microRNA 375	gene	MP:0009254	disorganized pancreatic islets		IAGP		N	RGD:5509061	20141003	MGI			PMID:19289822
1607645	Mir200b	microRNA 200b	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1607645	Mir200b	microRNA 200b	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1607645	Mir200b	microRNA 200b	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1607645	Mir200b	microRNA 200b	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1607645	Mir200b	microRNA 200b	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1607645	Mir200b	microRNA 200b	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1607645	Mir200b	microRNA 200b	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1607645	Mir200b	microRNA 200b	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1607645	Mir200b	microRNA 200b	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1607653	Mir125a	microRNA 125a	gene	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20160602	MGI			PMID:25963922
1607653	Mir125a	microRNA 125a	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20160602	MGI			PMID:25963922
1607653	Mir125a	microRNA 125a	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20160602	MGI			PMID:25963922
1607653	Mir125a	microRNA 125a	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25963922
1607653	Mir125a	microRNA 125a	gene	MP:0008681	increased interleukin-17 secretion		IAGP		N	RGD:5509061	20160602	MGI			PMID:25963922
1607661	Mir30a	microRNA 30a	gene	MP:0005666	abnormal adipose tissue physiology		IAGP		N	RGD:5509061	20241212	MGI			PMID:36243005
1607664	Mir29a	microRNA 29a	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20201001	MGI			PMID:30827505
1607664	Mir29a	microRNA 29a	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20201001	MGI			PMID:30827505
1607666	Mir27a	microRNA 27a	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20250612	MGI			PMID:30327467
1607666	Mir27a	microRNA 27a	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20250612	MGI			PMID:30327467
1607666	Mir27a	microRNA 27a	gene	MP:0008469	abnormal protein level		IAGP		N	RGD:5509061	20250612	MGI			PMID:30327467
1607666	Mir27a	microRNA 27a	gene	MP:0014537	increased calcium level		IAGP		N	RGD:5509061	20250612	MGI			PMID:30327467
1607666	Mir27a	microRNA 27a	gene	MP:0030941	enhanced autophagy		IAGP		N	RGD:5509061	20250612	MGI			PMID:30327467
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0005216	abnormal pancreatic alpha cell morphology		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0005491	pancreatic islet hyperplasia		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0009168	decreased pancreatic islet number		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0009171	enlarged pancreatic islets		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607668	Mir26a-1	microRNA 26a-1	gene	MP:0013279	increased fasting circulating glucose level		IAGP		N	RGD:5509061	20200416	MGI			PMID:32092075
1607673	Mir217	microRNA 217	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20191017	MGI			PMID:31367007
1607673	Mir217	microRNA 217	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20191017	MGI			PMID:31367007
1607673	Mir217	microRNA 217	gene	MP:0013221	pancreatic acinar-to-ductal metaplasia		IAGP		N	RGD:5509061	20191017	MGI			PMID:31367007
1607674	Mir216a	microRNA 216a	gene	MP:0004761	increased susceptibility to induced pancreatitis		IAGP		N	RGD:5509061	20191017	MGI			PMID:31367007
1607674	Mir216a	microRNA 216a	gene	MP:0009153	increased pancreas tumor incidence		IAGP		N	RGD:5509061	20191017	MGI			PMID:31367007
1607674	Mir216a	microRNA 216a	gene	MP:0013221	pancreatic acinar-to-ductal metaplasia		IAGP		N	RGD:5509061	20191017	MGI			PMID:31367007
1607676	Mir214	microRNA 214	gene	MP:0000343	abnormal response to cardiac infarction		IAGP		N	RGD:5509061	20190207	MGI			PMID:22426211
1607676	Mir214	microRNA 214	gene	MP:0003037	increased myocardial infarct size		IAGP		N	RGD:5509061	20190207	MGI			PMID:22426211
1607676	Mir214	microRNA 214	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20190207	MGI			PMID:22426211
1607676	Mir214	microRNA 214	gene	MP:0003222	increased cardiomyocyte apoptosis		IAGP		N	RGD:5509061	20190207	MGI			PMID:22426211
1607676	Mir214	microRNA 214	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20190207	MGI			PMID:22426211
1607676	Mir214	microRNA 214	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20190207	MGI			PMID:22426211
1607679	Mir211	microRNA 211	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20250403	MGI			PMID:36511897
1607679	Mir211	microRNA 211	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:36511897
1607680	Mir210	microRNA 210	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20201015	MGI			PMID:32141129
1607680	Mir210	microRNA 210	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23960236
1607680	Mir210	microRNA 210	gene	MP:0004794	increased anti-nuclear antigen antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23960236
1607680	Mir210	microRNA 210	gene	MP:0004829	increased anti-chromatin antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23960236
1607680	Mir210	microRNA 210	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23960236
1607680	Mir210	microRNA 210	gene	MP:0011290	decreased nephron number		IAGP		N	RGD:5509061	20201015	MGI			PMID:32141129
1607682	Mir208a	microRNA 208a	gene	MP:0001544	abnormal cardiovascular system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17379774
1607682	Mir208a	microRNA 208a	gene	MP:0003896	prolonged PR interval		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726871
1607682	Mir208a	microRNA 208a	gene	MP:0003921	abnormal heart left ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17379774
1607682	Mir208a	microRNA 208a	gene	MP:0004090	abnormal sarcomere morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17379774
1607682	Mir208a	microRNA 208a	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20141003	MGI			PMID:17379774
1607682	Mir208a	microRNA 208a	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17379774
1607682	Mir208a	microRNA 208a	gene	MP:0010510	absent P wave		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726871
1607682	Mir208a	microRNA 208a	gene	MP:0010519	atrioventricular block		IAGP		N	RGD:5509061	20141003	MGI			PMID:19726871
1607684	Mir205	microRNA 205	gene	MP:0000367	abnormal coat/ hair morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1607684	Mir205	microRNA 205	gene	MP:0000377	abnormal hair follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1607684	Mir205	microRNA 205	gene	MP:0000746	weakness		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1607684	Mir205	microRNA 205	gene	MP:0001199	thin skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:24116130
1607684	Mir205	microRNA 205	gene	MP:0001218	thin epidermis		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1607684	Mir205	microRNA 205	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24116130
1607684	Mir205	microRNA 205	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24116130
1607684	Mir205	microRNA 205	gene	MP:0001663	abnormal digestive system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1607684	Mir205	microRNA 205	gene	MP:0003704	abnormal hair follicle development		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1607684	Mir205	microRNA 205	gene	MP:0003853	dry skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:24116130
1607684	Mir205	microRNA 205	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20141003	MGI			PMID:24116130
1607684	Mir205	microRNA 205	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
1607684	Mir205	microRNA 205	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1607684	Mir205	microRNA 205	gene	MP:0008762	embryonic lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:22570807
1607684	Mir205	microRNA 205	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23974039
1607684	Mir205	microRNA 205	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24116130
1607685	Mir204	microRNA 204	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20220721	MGI			PMID:32487559
1607685	Mir204	microRNA 204	gene	MP:0002871	albuminuria		IAGP		N	RGD:5509061	20220721	MGI			PMID:32487559
1607685	Mir204	microRNA 204	gene	MP:0003215	renal interstitial fibrosis		IAGP		N	RGD:5509061	20220721	MGI			PMID:32487559
1607685	Mir204	microRNA 204	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20250403	MGI			PMID:36511897
1607685	Mir204	microRNA 204	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20220721	MGI			PMID:32487559
1607685	Mir204	microRNA 204	gene	MP:0011316	abnormal kidney interlobular artery morphology		IAGP		N	RGD:5509061	20220721	MGI			PMID:32487559
1607685	Mir204	microRNA 204	gene	MP:0014708	increased synovial pannus formation		IAGP		N	RGD:5509061	20250710	MGI			PMID:36511897
1607685	Mir204	microRNA 204	gene	MP:0021052	abnormal renal arterial blood pressure regulation		IAGP		N	RGD:5509061	20220721	MGI			PMID:32487559
1607688	Spata22	spermatogenesis associated 22	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20210128	MGI			
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001127	small ovary		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001146	abnormal testis morphology		IEA		N	RGD:5509061	20181227	MGI			
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001153	small seminiferous tubules		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001155	arrest of spermatogenesis		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001924	infertility		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001930	abnormal meiosis		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20181227	MGI			
1607688	Spata22	spermatogenesis associated 22	gene	MP:0002016	ovary cyst		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0002777	absent ovarian follicles		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20211021	MGI			
1607688	Spata22	spermatogenesis associated 22	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0004805	absent oocytes		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0004850	abnormal testis weight		IEA		N	RGD:5509061	20260402	MGI			
1607688	Spata22	spermatogenesis associated 22	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20181227	MGI			
1607688	Spata22	spermatogenesis associated 22	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0005159	azoospermia		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0005168	abnormal female meiosis		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0006379	abnormal spermatocyte morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0006380	abnormal spermatid morphology		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20190314	MGI			PMID:28297563
1607688	Spata22	spermatogenesis associated 22	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1607688	Spata22	spermatogenesis associated 22	gene	MP:0010948	abnormal double-strand DNA break repair		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20201224	MGI			PMID:32388826
1607688	Spata22	spermatogenesis associated 22	gene	MP:0014604	hemorrhagic ovary cyst		IAGP		N	RGD:5509061	20250206	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0014633	decreased spermatid number		IAGP		N	RGD:5509061	20250306	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:22011390
1607688	Spata22	spermatogenesis associated 22	gene	MP:0014764	impaired double-strand DNA break repair		IAGP		N	RGD:5509061	20250904	MGI			PMID:28297563
1607697	Klhl3	kelch-like 3	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28052936
1607697	Klhl3	kelch-like 3	gene	MP:0002666	increased circulating aldosterone level		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1607697	Klhl3	kelch-like 3	gene	MP:0002833	increased heart weight		IEA		N	RGD:5509061	20220811	MGI			
1607697	Klhl3	kelch-like 3	gene	MP:0002874	decreased hemoglobin content		IEA		N	RGD:5509061	20170105	MGI			
1607697	Klhl3	kelch-like 3	gene	MP:0002968	increased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1607697	Klhl3	kelch-like 3	gene	MP:0003017	decreased circulating bicarbonate level		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1607697	Klhl3	kelch-like 3	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28052936
1607697	Klhl3	kelch-like 3	gene	MP:0003019	increased circulating chloride level		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1607697	Klhl3	kelch-like 3	gene	MP:0003030	acidemia		IAGP		N	RGD:5509061	20180607	MGI			PMID:28052936
1607697	Klhl3	kelch-like 3	gene	MP:0003030	acidemia		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1607697	Klhl3	kelch-like 3	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20150827	MGI			PMID:24821705
1607697	Klhl3	kelch-like 3	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20180607	MGI			PMID:28052936
1607697	Klhl3	kelch-like 3	gene	MP:0004757	abnormal distal convoluted tubule morphology		IAGP		N	RGD:5509061	20180607	MGI			PMID:28052936
1607697	Klhl3	kelch-like 3	gene	MP:0005583	decreased renin activity		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1607697	Klhl3	kelch-like 3	gene	MP:0005618	decreased urine potassium level		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1607697	Klhl3	kelch-like 3	gene	MP:0005627	increased circulating potassium level		IAGP		N	RGD:5509061	20180607	MGI			PMID:28052936
1607697	Klhl3	kelch-like 3	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1607697	Klhl3	kelch-like 3	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1607697	Klhl3	kelch-like 3	gene	MP:0012339	hyperkalemia		IAGP		N	RGD:5509061	20150827	MGI			PMID:24821705
1607697	Klhl3	kelch-like 3	gene	MP:0012339	hyperkalemia		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1607697	Klhl3	kelch-like 3	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20150827	MGI			PMID:24821705
1607697	Klhl3	kelch-like 3	gene	MP:0012551	metabolic acidosis		IAGP		N	RGD:5509061	20200402	MGI			PMID:30148674
1608040	Lexis1	lipid responsive LXR-induced inhibitor of cholesterol synthesis 1	gene	MP:0002628	hepatic steatosis		IAGP		N	RGD:5509061	20171116	MGI			PMID:27251289
1608040	Lexis1	lipid responsive LXR-induced inhibitor of cholesterol synthesis 1	gene	MP:0010027	increased liver cholesterol level		IAGP		N	RGD:5509061	20171116	MGI			PMID:27251289
1608088	5430431A17Rik	RIKEN cDNA 5430431A17 gene	gene	MP:0000275	heart hyperplasia		IAGP		N	RGD:5509061	20181206	MGI			PMID:30177572
1608088	5430431A17Rik	RIKEN cDNA 5430431A17 gene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20181206	MGI			PMID:30177572
1608088	5430431A17Rik	RIKEN cDNA 5430431A17 gene	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20181206	MGI			PMID:30177572
1608088	5430431A17Rik	RIKEN cDNA 5430431A17 gene	gene	MP:0002953	thick ventricular wall		IAGP		N	RGD:5509061	20181206	MGI			PMID:30177572
1608088	5430431A17Rik	RIKEN cDNA 5430431A17 gene	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20181206	MGI			PMID:30177572
1608088	5430431A17Rik	RIKEN cDNA 5430431A17 gene	gene	MP:0003649	decreased heart right ventricle size		IAGP		N	RGD:5509061	20181206	MGI			PMID:30177572
1608088	5430431A17Rik	RIKEN cDNA 5430431A17 gene	gene	MP:0006143	increased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20181206	MGI			PMID:30177572
1608088	5430431A17Rik	RIKEN cDNA 5430431A17 gene	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20181206	MGI			PMID:30177572
1608088	5430431A17Rik	RIKEN cDNA 5430431A17 gene	gene	MP:0010580	decreased heart left ventricle size		IAGP		N	RGD:5509061	20181206	MGI			PMID:30177572
1608089	Krtap7-1	keratin associated protein 7-1	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1608089	Krtap7-1	keratin associated protein 7-1	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1608089	Krtap7-1	keratin associated protein 7-1	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230119	MGI			
1608089	Krtap7-1	keratin associated protein 7-1	gene	MP:0000692	small spleen		IEA		N	RGD:5509061	20230119	MGI			
1608089	Krtap7-1	keratin associated protein 7-1	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230119	MGI			
1608089	Krtap7-1	keratin associated protein 7-1	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230119	MGI			
1608089	Krtap7-1	keratin associated protein 7-1	gene	MP:0001312	abnormal cornea morphology		IEA		N	RGD:5509061	20260402	MGI			
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0000280	thin ventricular wall		IAGP		N	RGD:5509061	20141003	MGI			PMID:23369715
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0000467	abnormal esophagus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0001176	abnormal lung development		IAGP		N	RGD:5509061	20161229	MGI			PMID:25909911
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0001178	pulmonary hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0001633	poor circulation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23369715
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0001954	respiratory distress		IAGP		N	RGD:5509061	20161229	MGI			PMID:25909911
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0002270	abnormal pulmonary alveolus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0003052	omphalocele		IAGP		N	RGD:5509061	20141003	MGI			PMID:23369715
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0003159	abnormal esophageal smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0003384	abnormal ventral body wall morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23369715
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0003641	small lung		IAGP		N	RGD:5509061	20161229	MGI			PMID:25909911
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0004007	abnormal lung vasculature morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0010402	ventricular septal defect		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0010502	ventricle myocardium hypoplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:23369715
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0010975	abnormal lung lobe morphology		IAGP		N	RGD:5509061	20161229	MGI			PMID:25909911
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20161229	MGI			PMID:25909911
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:23369715
1608137	Fendrr	Foxf1 adjacent non-coding developmental regulatory RNA	gene	MP:0011395	decreased fetal cardiomyocyte proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23369715
1608160	Mir324	microRNA 324	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20221201	MGI			PMID:34001919
1608161	Mir31	microRNA 31	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0001881	abnormal mammary gland physiology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0004135	abnormal mammary gland embryonic development		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0006269	abnormal mammary gland growth during pregnancy		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0010269	decreased mammary gland tumor incidence		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0013716	hypolactation		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608161	Mir31	microRNA 31	gene	MP:0013782	abnormal mammary duct terminal end bud morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:29051494
1608163	Mir10a	microRNA 10a	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24204315
1608163	Mir10a	microRNA 10a	gene	MP:0002404	increased intestinal adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24204315
1608163	Mir10a	microRNA 10a	gene	MP:0010279	increased gastrointestinal tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:24204315
1608164	Mir100	microRNA 100	gene	MP:0001860	liver inflammation		IAGP		N	RGD:5509061	20200402	MGI			PMID:31293973
1608164	Mir100	microRNA 100	gene	MP:0002075	abnormal coat/hair pigmentation		IEA		N	RGD:5509061	20230601	MGI			
1608164	Mir100	microRNA 100	gene	MP:0002941	increased circulating alanine transaminase level		IAGP		N	RGD:5509061	20200402	MGI			PMID:31293973
1608164	Mir100	microRNA 100	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20200402	MGI			PMID:31293973
1608164	Mir100	microRNA 100	gene	MP:0011239	abnormal skin coloration		IEA		N	RGD:5509061	20230601	MGI			
1608164	Mir100	microRNA 100	gene	MP:0020427	increased hepatocyte karyomegaly		IAGP		N	RGD:5509061	20200402	MGI			PMID:31293973
1608167	Mir378a	microRNA 378a	gene	MP:0001552	increased circulating triglyceride level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0004889	increased energy expenditure		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0005560	decreased circulating glucose level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0005659	decreased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0008844	decreased subcutaneous adipose tissue amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0010025	decreased total body fat amount		IAGP		N	RGD:5509061	20141003	MGI			PMID:22949648
1608167	Mir378a	microRNA 378a	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20210610	MGI			PMID:22949648
1608170	Mir96	microRNA 96	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0001410	head bobbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0001485	abnormal pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0001967	deafness		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20180830	MGI			
1608170	Mir96	microRNA 96	gene	MP:0004362	cochlear hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0004404	cochlear outer hair cell degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0004408	decreased cochlear hair cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0004416	absent cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0004417	decreased cochlear nerve compound action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0004516	fused vestibular hair cell stereocilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0004521	abnormal cochlear hair cell stereociliary bundle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0006325	impaired hearing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608170	Mir96	microRNA 96	gene	MP:0006358	absent pinna reflex		IAGP		N	RGD:5509061	20141003	MGI			PMID:19363478
1608173	Mir7b	microRNA 7b	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190523	MGI			PMID:29887379
1608180	Mir485	microRNA 485	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20231109	MGI			PMID:36161914
1608180	Mir485	microRNA 485	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36161914
1608180	Mir485	microRNA 485	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20231109	MGI			PMID:36161914
1608180	Mir485	microRNA 485	gene	MP:0009119	increased brown fat cell size		IAGP		N	RGD:5509061	20231109	MGI			PMID:36161914
1608180	Mir485	microRNA 485	gene	MP:0009128	decreased brown fat cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:36161914
1608185	Mir451a	microRNA 451a	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679397
1608185	Mir451a	microRNA 451a	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0001586	abnormal erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679397
1608185	Mir451a	microRNA 451a	gene	MP:0002396	abnormal hematopoietic system morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679397
1608185	Mir451a	microRNA 451a	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679397
1608185	Mir451a	microRNA 451a	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0011171	increased number of Heinz bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0011241	abnormal fetal derived definitive erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679397
1608185	Mir451a	microRNA 451a	gene	MP:0011594	decreased catalase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608185	Mir451a	microRNA 451a	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:20513743
1608185	Mir451a	microRNA 451a	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:20513743
1608186	Mir449a	microRNA 449a	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20191003	MGI			PMID:29162901
1608189	Mir429	microRNA 429	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1608189	Mir429	microRNA 429	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1608189	Mir429	microRNA 429	gene	MP:0002680	decreased corpora lutea number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1608189	Mir429	microRNA 429	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1608189	Mir429	microRNA 429	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1608189	Mir429	microRNA 429	gene	MP:0005132	decreased luteinizing hormone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1608189	Mir429	microRNA 429	gene	MP:0005185	decreased circulating progesterone level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1608189	Mir429	microRNA 429	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1608189	Mir429	microRNA 429	gene	MP:0009017	prolonged estrus		IAGP		N	RGD:5509061	20141003	MGI			PMID:23765281
1608190	Mir425	microRNA 425	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20191128	MGI			PMID:31383850
1608190	Mir425	microRNA 425	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20191128	MGI			PMID:31383850
1608190	Mir425	microRNA 425	gene	MP:0009747	impaired behavioral response to xenobiotic		IAGP		N	RGD:5509061	20191128	MGI			PMID:31383850
1608190	Mir425	microRNA 425	gene	MP:0011451	increased susceptibility to dopaminergic neuron neurotoxicity		IAGP		N	RGD:5509061	20191128	MGI			PMID:31383850
1608192	Mir409	microRNA 409	gene	MP:0003038	decreased myocardial infarct size		IAGP		N	RGD:5509061	20250102	MGI			PMID:37332476
1608192	Mir409	microRNA 409	gene	MP:0003710	abnormal physiological neovascularization		IAGP		N	RGD:5509061	20250102	MGI			PMID:37332476
1608192	Mir409	microRNA 409	gene	MP:0031216	decreased susceptibility to myocardial ischemic injury		IAGP		N	RGD:5509061	20250102	MGI			PMID:37332476
1608196	Mir379	microRNA 379	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20240627	MGI			PMID:33398021
1608196	Mir379	microRNA 379	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20240627	MGI			PMID:33398021
1608206	Mir34a	microRNA 34a	gene	MP:0000716	abnormal immune system cell morphology		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0001344	blepharoptosis		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0001401	jumpy		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0001505	hunched posture		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0001866	nasal inflammation		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22564414
1608206	Mir34a	microRNA 34a	gene	MP:0002169	no abnormal phenotype detected		IEA		N	RGD:5509061	20141003	MGI			
1608206	Mir34a	microRNA 34a	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0003312	abnormal locomotor coordination		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0003700	abnormal oviduct transport		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0003998	decreased thermal nociceptive threshold		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20150226	MGI			PMID:24642471
1608206	Mir34a	microRNA 34a	gene	MP:0004728	abnormal efferent ductules of testis morphology		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0004948	abnormal neuronal precursor proliferation		IAGP		N	RGD:5509061	20141003	MGI			PMID:22160706
1608206	Mir34a	microRNA 34a	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22564414
1608206	Mir34a	microRNA 34a	gene	MP:0005014	increased B cell number		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0005574	decreased pulmonary respiratory rate		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0005576	decreased pulmonary ventilation		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0005605	increased bone mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:22564414
1608206	Mir34a	microRNA 34a	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22020437
1608206	Mir34a	microRNA 34a	gene	MP:0006283	increased medulloblastoma incidence		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0008489	slow postnatal weight gain		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20160922	MGI			PMID:25348795
1608206	Mir34a	microRNA 34a	gene	MP:0011053	decreased respiratory motile cilia number		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20210520	MGI			PMID:33787491
1608206	Mir34a	microRNA 34a	gene	MP:0011644	abnormal oviduct epithelium motile cilium morphology		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0012018	abnormal oviduct physiology		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608206	Mir34a	microRNA 34a	gene	MP:0014200	abnormal respiratory epithelium physiology		IAGP		N	RGD:5509061	20180329	MGI			PMID:28923932
1608209	Mir338	microRNA 338	gene	MP:0004985	decreased osteoclast cell number		IAGP		N	RGD:5509061	20200423	MGI			PMID:31281513
1608209	Mir338	microRNA 338	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20200423	MGI			PMID:31281513
1608209	Mir338	microRNA 338	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20200423	MGI			PMID:31281513
1608209	Mir338	microRNA 338	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20200423	MGI			PMID:31281513
1608212	Mir326	microRNA 326	gene	MP:0003204	decreased neuron apoptosis		IAGP		N	RGD:5509061	20241017	MGI			PMID:38909535
1608212	Mir326	microRNA 326	gene	MP:0006058	decreased cerebral infarct size		IAGP		N	RGD:5509061	20241017	MGI			PMID:38909535
1608212	Mir326	microRNA 326	gene	MP:0006059	decreased susceptibility to ischemic brain injury		IAGP		N	RGD:5509061	20241017	MGI			PMID:38909535
1608214	Mir320	microRNA 320	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1608215	Mir32	microRNA 32	gene	MP:0000183	decreased circulating LDL cholesterol level		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0000609	abnormal liver physiology		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0002891	increased insulin sensitivity		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0002942	decreased circulating alanine transaminase level		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0003402	decreased liver weight		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0005179	decreased circulating cholesterol level		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0005632	decreased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0009356	decreased liver triglyceride level		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0010026	decreased liver cholesterol level		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0013245	abnormal lipid metabolism		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0031268	decreased susceptibility to diet-induced hepatic steatosis		IAGP		N	RGD:5509061	20240222	MGI			PMID:37451670
1608215	Mir32	microRNA 32	gene	MP:0031601	decreased endoplasmic reticulum stress		IAGP		N	RGD:5509061	20240418	MGI			PMID:37451670
1608218	Mir301	microRNA 301	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20170216	MGI			PMID:27462406
1608218	Mir301	microRNA 301	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20170216	MGI			PMID:27462406
1608218	Mir301	microRNA 301	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20170216	MGI			PMID:27462406
1608218	Mir301	microRNA 301	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20170216	MGI			PMID:27462406
1608218	Mir301	microRNA 301	gene	MP:0005671	abnormal response to transplant		IAGP		N	RGD:5509061	20170216	MGI			PMID:27462406
1608218	Mir301	microRNA 301	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20170216	MGI			PMID:27462406
1608218	Mir301	microRNA 301	gene	MP:0010268	decreased lymphoma incidence		IAGP		N	RGD:5509061	20170216	MGI			PMID:27462406
1608218	Mir301	microRNA 301	gene	MP:0010285	decreased skin tumor incidence		IAGP		N	RGD:5509061	20170216	MGI			PMID:27462406
1608229	Mir218-1	microRNA 218-1	gene	MP:0000160	kyphosis		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0000937	abnormal motor neuron morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0000938	motor neuron degeneration		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0000939	decreased motor neuron number		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0000940	abnormal motor neuron innervation pattern		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0001054	failure of neuromuscular synapse presynaptic differentiation		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0001953	respiratory failure		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0002690	akinesia		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0003043	hypoalgesia		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608229	Mir218-1	microRNA 218-1	gene	MP:0020336	abnormal motor neuron dendrite morphology		IAGP		N	RGD:5509061	20170824	MGI			PMID:26680198
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0000745	tremors		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0001406	abnormal gait		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0001492	abnormal pilomotor reflex		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0001951	abnormal breathing pattern		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608230	Mir199a-2	microRNA 199a-2	gene	MP:0009939	abnormal hippocampus neuron morphology		IAGP		N	RGD:5509061	20190912	MGI			PMID:26344767
1608231	Mir196b	microRNA 196b	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1608231	Mir196b	microRNA 196b	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1608231	Mir196b	microRNA 196b	gene	MP:0004616	lumbar vertebral transformation		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1608231	Mir196b	microRNA 196b	gene	MP:0004617	sacral vertebral transformation		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1608231	Mir196b	microRNA 196b	gene	MP:0010113	abnormal sacrum morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1608234	Mir133b	microRNA 133b	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:22875923
1608236	Mir128-2	microRNA 128-2	gene	MP:0001399	hyperactivity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24311694
1608236	Mir128-2	microRNA 128-2	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:24311694
1608236	Mir128-2	microRNA 128-2	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:24311694
1608236	Mir128-2	microRNA 128-2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24311694
1608236	Mir128-2	microRNA 128-2	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:24311694
1608236	Mir128-2	microRNA 128-2	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20141003	MGI			PMID:24311694
1608236	Mir128-2	microRNA 128-2	gene	MP:0021019	increased dendritic spine number		IAGP		N	RGD:5509061	20211014	MGI			PMID:24311694
1608237	Mir223	microRNA 223	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278031
1608237	Mir223	microRNA 223	gene	MP:0000322	increased granulocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278031
1608237	Mir223	microRNA 223	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278031
1608237	Mir223	microRNA 223	gene	MP:0002415	abnormal neutrophil differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278031
1608237	Mir223	microRNA 223	gene	MP:0002462	abnormal granulocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278031
1608237	Mir223	microRNA 223	gene	MP:0002463	abnormal neutrophil physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278031
1608237	Mir223	microRNA 223	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18278031
1608292	Mir203	microRNA 203	gene	MP:0001200	thick skin		IAGP		N	RGD:5509061	20151224	MGI			PMID:26203562
1608292	Mir203	microRNA 203	gene	MP:0001417	decreased exploration in new environment		IEA		N	RGD:5509061	20260528	MGI			
1608292	Mir203	microRNA 203	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20151217	MGI			PMID:26203562
1608292	Mir203	microRNA 203	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20151224	MGI			PMID:26203562
1608292	Mir203	microRNA 203	gene	MP:0010308	decreased tumor latency		IAGP		N	RGD:5509061	20151224	MGI			PMID:26203562
1608292	Mir203	microRNA 203	gene	MP:0013279	increased fasting circulating glucose level		IEA		N	RGD:5509061	20260528	MGI			
1608293	Mir202	microRNA 202	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0001154	seminiferous tubule degeneration		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0004901	decreased male germ cell number		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0005169	abnormal male meiosis		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0008261	arrest of male meiosis		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0008967	absent chiasmata formation		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0009451	abnormal chromosomal synapsis		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0009452	abnormal synaptonemal complex		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0011751	abnormal X-Y chromosome synapsis during male meiosis		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608293	Mir202	microRNA 202	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20230817	MGI			PMID:35712867
1608300	Mir196a-1	microRNA 196a-1	gene	MP:0000480	increased rib number		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1608300	Mir196a-1	microRNA 196a-1	gene	MP:0003036	vertebral transformation		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1608300	Mir196a-1	microRNA 196a-1	gene	MP:0004672	short ribs		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1608300	Mir196a-1	microRNA 196a-1	gene	MP:0010113	abnormal sacrum morphology		IAGP		N	RGD:5509061	20161117	MGI			PMID:26283362
1608301	Mir195a	microRNA 195a	gene	MP:0031384	impaired blood-brain barrier function		IAGP		N	RGD:5509061	20220407	MGI			PMID:33029941
1608304	Mir192	microRNA 192	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649518
1608304	Mir192	microRNA 192	gene	MP:0005325	abnormal renal glomerulus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649518
1608304	Mir192	microRNA 192	gene	MP:0006315	abnormal urine protein level		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649518
1608304	Mir192	microRNA 192	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649518
1608304	Mir192	microRNA 192	gene	MP:0011338	abnormal mesangial matrix morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23649518
1608308	Mir188	microRNA 188	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0004149	increased bone strength		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0004988	increased osteoblast cell number		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0009115	abnormal fat cell morphology		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0010878	increased trabecular bone volume		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0011168	abnormal fat cell differentiation		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0013621	decreased internal diameter of femur		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0013623	increased femur compact bone thickness		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0013640	increased bone stiffness		IAGP		N	RGD:5509061	20160505	MGI			PMID:25751060
1608308	Mir188	microRNA 188	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20160609	MGI			PMID:25751060
1608311	Mir185	microRNA 185	gene	MP:0000062	increased bone mineral density		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0009347	increased trabecular bone thickness		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0010868	increased bone trabecula number		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0010875	increased bone volume		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0010933	decreased trabecular bone connectivity density		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0011584	increased alkaline phosphatase activity		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0011710	enhanced osteoblast differentiation		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0012072	decreased susceptibility to osteoporosis		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0013631	decreased bone trabecular spacing		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0020039	increased bone ossification		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608311	Mir185	microRNA 185	gene	MP:0030438	increased osteoblast proliferation		IAGP		N	RGD:5509061	20191024	MGI			PMID:30787286
1608312	Mir184	microRNA 184	gene	MP:0002079	increased circulating insulin level		IAGP		N	RGD:5509061	20141009	MGI			PMID:24361012
1608312	Mir184	microRNA 184	gene	MP:0003058	increased insulin secretion		IAGP		N	RGD:5509061	20141009	MGI			PMID:24361012
1608312	Mir184	microRNA 184	gene	MP:0005292	improved glucose tolerance		IAGP		N	RGD:5509061	20141009	MGI			PMID:24361012
1608312	Mir184	microRNA 184	gene	MP:0009113	increased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141009	MGI			PMID:24361012
1608312	Mir184	microRNA 184	gene	MP:0011819	increased pancreatic beta cell proliferation		IAGP		N	RGD:5509061	20141009	MGI			PMID:24361012
1608312	Mir184	microRNA 184	gene	MP:0013278	decreased fasting circulating glucose level		IAGP		N	RGD:5509061	20141009	MGI			PMID:24361012
1608313	Mir183	microRNA 183	gene	MP:0012143	decreased a-wave amplitude		IAGP		N	RGD:5509061	20210506	MGI			PMID:32176259
1608313	Mir183	microRNA 183	gene	MP:0012144	decreased b-wave amplitude		IAGP		N	RGD:5509061	20210506	MGI			PMID:32176259
1608314	Mir182	microRNA 182	gene	MP:0001273	decreased metastatic potential		IAGP		N	RGD:5509061	20160204	MGI			PMID:25180607
1608314	Mir182	microRNA 182	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20160204	MGI			PMID:25180607
1608318	Mir155	microRNA 155	gene	MP:0000685	abnormal immune system morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0001175	abnormal lung morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0001800	abnormal humoral immune response		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150305	MGI			PMID:25367574
1608318	Mir155	microRNA 155	gene	MP:0002267	abnormal bronchiole morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0002376	abnormal dendritic cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0002378	abnormal gut-associated lymphoid tissue morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0002391	abnormal Peyer's patch germinal center morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0002412	increased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0002432	abnormal CD4-positive, alpha beta T cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0002433	abnormal T-helper 1 cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0002444	abnormal T cell physiology		IAGP		N	RGD:5509061	20160218	MGI			PMID:26163372
1608318	Mir155	microRNA 155	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0004800	decreased susceptibility to experimental autoimmune encephalomyelitis		IAGP		N	RGD:5509061	20160218	MGI			PMID:26163372
1608318	Mir155	microRNA 155	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0004816	abnormal class switch recombination		IAGP		N	RGD:5509061	20141003	MGI			PMID:18455451
1608318	Mir155	microRNA 155	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19234151
1608318	Mir155	microRNA 155	gene	MP:0004974	decreased regulatory T cell number		IAGP		N	RGD:5509061	20160218	MGI			PMID:26163372
1608318	Mir155	microRNA 155	gene	MP:0005463	abnormal CD4-positive, alpha-beta T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0008090	increased T-helper 2 cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0008178	decreased germinal center B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0008192	abnormal germinal center B cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0008482	decreased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0008484	decreased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0008495	decreased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463290
1608318	Mir155	microRNA 155	gene	MP:0008561	decreased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0008660	increased interleukin-10 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:17463289
1608318	Mir155	microRNA 155	gene	MP:0008706	decreased interleukin-6 secretion		IAGP		N	RGD:5509061	20160218	MGI			PMID:26163372
1608318	Mir155	microRNA 155	gene	MP:0008866	chromosomal instability		IAGP		N	RGD:5509061	20141003	MGI			PMID:18455451
1608318	Mir155	microRNA 155	gene	MP:0010220	decreased T-helper 17 cell number		IAGP		N	RGD:5509061	20160218	MGI			PMID:26163372
1608318	Mir155	microRNA 155	gene	MP:0010221	abnormal T-helper 17 cell differentiation		IAGP		N	RGD:5509061	20160218	MGI			PMID:26163372
1608318	Mir155	microRNA 155	gene	MP:0013771	decreased effector memory T-helper cell number		IAGP		N	RGD:5509061	20160218	MGI			PMID:26163372
1608323	Mir150	microRNA 150	gene	MP:0002494	increased IgM level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923094
1608323	Mir150	microRNA 150	gene	MP:0002495	increased IgA level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923094
1608323	Mir150	microRNA 150	gene	MP:0004977	increased B-1 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923094
1608323	Mir150	microRNA 150	gene	MP:0008207	decreased B-2 B cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923094
1608323	Mir150	microRNA 150	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923094
1608323	Mir150	microRNA 150	gene	MP:0008501	increased IgG2b level		IAGP		N	RGD:5509061	20141003	MGI			PMID:17923094
1608324	Mir149	microRNA 149	gene	MP:0003887	increased hepatocyte apoptosis		IAGP		N	RGD:5509061	20201001	MGI			PMID:29029439
1608324	Mir149	microRNA 149	gene	MP:0003893	increased hepatocyte proliferation		IAGP		N	RGD:5509061	20201001	MGI			PMID:29029439
1608324	Mir149	microRNA 149	gene	MP:0005343	increased circulating aspartate transaminase level		IAGP		N	RGD:5509061	20201001	MGI			PMID:29029439
1608324	Mir149	microRNA 149	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20201001	MGI			PMID:29029439
1608325	Mir148a	microRNA 148a	gene	MP:0001805	decreased IgG level		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608325	Mir148a	microRNA 148a	gene	MP:0001806	decreased IgM level		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608325	Mir148a	microRNA 148a	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608325	Mir148a	microRNA 148a	gene	MP:0002459	abnormal B cell physiology		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608325	Mir148a	microRNA 148a	gene	MP:0003926	decreased cellular glucose uptake		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608325	Mir148a	microRNA 148a	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608325	Mir148a	microRNA 148a	gene	MP:0008098	decreased plasma cell number		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608325	Mir148a	microRNA 148a	gene	MP:0008728	increased memory B cell number		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608325	Mir148a	microRNA 148a	gene	MP:0013940	abnormal plasmablast number		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608325	Mir148a	microRNA 148a	gene	MP:0020154	impaired humoral immune response		IAGP		N	RGD:5509061	20210826	MGI			PMID:33336366
1608327	Mir146	microRNA 146	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0000221	decreased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0000222	decreased neutrophil cell number		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1608327	Mir146	microRNA 146	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0000223	decreased monocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0000240	extramedullary hematopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0000321	increased bone marrow cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0000702	enlarged lymph nodes		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0001790	abnormal immune system physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0001828	abnormal T cell activation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0001852	conjunctivitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0002020	increased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0002023	increased B cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0002398	abnormal bone marrow cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0002401	abnormal lymphopoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0002451	abnormal macrophage physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0002493	increased IgG level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30013024
1608327	Mir146	microRNA 146	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0003179	thrombocytopenia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0003786	premature aging		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0003945	abnormal lymphocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0004762	increased anti-double stranded DNA antibody level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30013024
1608327	Mir146	microRNA 146	gene	MP:0004808	abnormal hematopoietic stem cell morphology		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1608327	Mir146	microRNA 146	gene	MP:0004946	abnormal regulatory T cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0004973	increased regulatory T cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0005000	abnormal immune tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0005016	decreased lymphocyte cell number		IAGP		N	RGD:5509061	20171102	MGI			PMID:26458771
1608327	Mir146	microRNA 146	gene	MP:0005088	increased acute inflammation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0005251	blepharitis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0005649	increased spleen neoplasm incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0008097	increased plasma cell number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30013024
1608327	Mir146	microRNA 146	gene	MP:0008177	increased germinal center B cell number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30013024
1608327	Mir146	microRNA 146	gene	MP:0008470	abnormal spleen B cell follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008481	increased spleen germinal center number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008483	increased spleen germinal center size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008499	increased IgG1 level		IAGP		N	RGD:5509061	20190926	MGI			PMID:30013024
1608327	Mir146	microRNA 146	gene	MP:0008553	increased circulating tumor necrosis factor level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008560	increased tumor necrosis factor secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008567	decreased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0008593	increased circulating interleukin-10 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008596	increased circulating interleukin-6 level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008641	increased circulating interleukin-1 beta level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008657	increased interleukin-1 beta secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008705	increased interleukin-6 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0008735	increased susceptibility to endotoxin shock		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0009317	increased follicular lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0009439	increased myeloid sarcoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0009788	increased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0010186	increased T follicular helper cell number		IAGP		N	RGD:5509061	20190926	MGI			PMID:30013024
1608327	Mir146	microRNA 146	gene	MP:0010296	increased hemolymphoid system tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20850013
1608327	Mir146	microRNA 146	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0010373	myeloid hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608327	Mir146	microRNA 146	gene	MP:0011076	increased macrophage nitric oxide production		IAGP		N	RGD:5509061	20141003	MGI			PMID:21555486
1608327	Mir146	microRNA 146	gene	MP:0011747	myelofibrosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576471
1608328	Mir145a	microRNA 145a	gene	MP:0001394	circling		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0002064	seizures		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0002834	decreased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0002976	vascular smooth muscle hypotrophy		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0005294	abnormal heart ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0005592	abnormal vascular smooth muscle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0006264	decreased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608328	Mir145a	microRNA 145a	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608329	Mir144	microRNA 144	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0000245	abnormal erythropoiesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0000693	spleen hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0002591	decreased mean corpuscular volume		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0002640	reticulocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0002642	anisocytosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0002874	decreased hemoglobin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0002875	decreased erythrocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0003135	increased erythroid progenitor cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0004952	increased spleen weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0005097	polychromatophilia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0005562	decreased mean corpuscular hemoglobin		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0008406	increased cellular sensitivity to hydrogen peroxide induced cell death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0008872	abnormal physiological response to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0010067	increased red blood cell distribution width		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0011171	increased number of Heinz bodies		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0011594	decreased catalase activity		IAGP		N	RGD:5509061	20141003	MGI			PMID:20679398
1608329	Mir144	microRNA 144	gene	MP:0015013	impaired bone marrow erythropoiesis		IAGP		N	RGD:5509061	20260611	MGI			PMID:20513743
1608329	Mir144	microRNA 144	gene	MP:0031276	abnormal stress erythropoiesis		IAGP		N	RGD:5509061	20260514	MGI			PMID:20513743
1608330	Mir143	microRNA 143	gene	MP:0004883	abnormal vascular wound healing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19720868
1608330	Mir143	microRNA 143	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20231207	MGI			
1608332	Mir140	microRNA 140	gene	MP:0000060	delayed bone ossification		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608332	Mir140	microRNA 140	gene	MP:0000097	short maxilla		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0000164	abnormal cartilage development		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608332	Mir140	microRNA 140	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0000445	short snout		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608332	Mir140	microRNA 140	gene	MP:0001255	decreased body height		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608332	Mir140	microRNA 140	gene	MP:0001533	abnormal skeleton physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0002113	abnormal skeleton development		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0002764	short tibia		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0003055	abnormal long bone epiphyseal plate morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608332	Mir140	microRNA 140	gene	MP:0003109	short femur		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0003408	increased width of hypertrophic chondrocyte zone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0003560	osteoarthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0003724	increased susceptibility to induced arthritis		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0004462	small basisphenoid bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0004471	short nasal bone		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608332	Mir140	microRNA 140	gene	MP:0004670	small vertebral body		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608332	Mir140	microRNA 140	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0004686	decreased length of long bones		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0005508	abnormal skeleton morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0006395	abnormal epiphyseal plate morphology		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608332	Mir140	microRNA 140	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0006396	decreased long bone epiphyseal plate size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0008525	decreased cranium height		IAGP		N	RGD:5509061	20190926	MGI			PMID:29695789
1608332	Mir140	microRNA 140	gene	MP:0009780	abnormal chondrocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:20466812
1608332	Mir140	microRNA 140	gene	MP:0010029	abnormal basicranium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21576357
1608332	Mir140	microRNA 140	gene	MP:0011175	platyspondylia		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608332	Mir140	microRNA 140	gene	MP:0020137	decreased bone mineralization		IAGP		N	RGD:5509061	20200604	MGI			PMID:30804514
1608333	Mir139	microRNA 139	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20191128	MGI			PMID:27022656
1608333	Mir139	microRNA 139	gene	MP:0004499	increased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20201119	MGI			PMID:26859226
1608333	Mir139	microRNA 139	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20191128	MGI			PMID:27022656
1608333	Mir139	microRNA 139	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20201119	MGI			PMID:26859226
1608333	Mir139	microRNA 139	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20201119	MGI			PMID:26859226
1608333	Mir139	microRNA 139	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20201119	MGI			PMID:26859226
1608333	Mir139	microRNA 139	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20191128	MGI			PMID:27022656
1608333	Mir139	microRNA 139	gene	MP:0009763	increased susceptibility to induced morbidity/mortality		IAGP		N	RGD:5509061	20201119	MGI			PMID:26859226
1608333	Mir139	microRNA 139	gene	MP:0009766	increased susceptibility to xenobiotic induced morbidity/mortality		IAGP		N	RGD:5509061	20191128	MGI			PMID:27022656
1608333	Mir139	microRNA 139	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20191128	MGI			PMID:27022656
1608333	Mir139	microRNA 139	gene	MP:0010180	increased susceptibility to weight loss		IAGP		N	RGD:5509061	20201119	MGI			PMID:26859226
1608333	Mir139	microRNA 139	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20191128	MGI			PMID:27022656
1608333	Mir139	microRNA 139	gene	MP:0013298	increased susceptibility to colitis induced morbidity/mortality		IAGP		N	RGD:5509061	20201119	MGI			PMID:26859226
1608333	Mir139	microRNA 139	gene	MP:0013956	decreased colon length		IAGP		N	RGD:5509061	20201119	MGI			PMID:26859226
1608333	Mir139	microRNA 139	gene	MP:0014234	decreased enterocyte apoptosis		IAGP		N	RGD:5509061	20230323	MGI			PMID:27022656
1608335	Mir137	microRNA 137	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20180315	MGI			PMID:25016316
1608342	Mir128-1	microRNA 128-1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:24311694
1608343	Mir127	microRNA 127	gene	MP:0001716	abnormal placenta labyrinth morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26138477
1608343	Mir127	microRNA 127	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20160915	MGI			PMID:26138477
1608343	Mir127	microRNA 127	gene	MP:0004201	fetal growth retardation		IAGP		N	RGD:5509061	20160915	MGI			PMID:26138477
1608343	Mir127	microRNA 127	gene	MP:0004265	abnormal placental transport		IAGP		N	RGD:5509061	20160915	MGI			PMID:26138477
1608343	Mir127	microRNA 127	gene	MP:0004920	increased placenta weight		IAGP		N	RGD:5509061	20160915	MGI			PMID:26138477
1608343	Mir127	microRNA 127	gene	MP:0004921	decreased placenta weight		IAGP		N	RGD:5509061	20160915	MGI			PMID:26138477
1608343	Mir127	microRNA 127	gene	MP:0009703	decreased birth body size		IAGP		N	RGD:5509061	20160915	MGI			PMID:26138477
1608343	Mir127	microRNA 127	gene	MP:0011088	neonatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20160915	MGI			PMID:26138477
1608343	Mir127	microRNA 127	gene	MP:0011526	abnormal placenta fetal blood space morphology		IAGP		N	RGD:5509061	20160915	MGI			PMID:26138477
1608344	Mir126a	microRNA 126a	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20241212	MGI			PMID:34931339
1608344	Mir126a	microRNA 126a	gene	MP:0001193	psoriasis		IAGP		N	RGD:5509061	20241212	MGI			PMID:34931339
1608344	Mir126a	microRNA 126a	gene	MP:0001194	dermatitis		IAGP		N	RGD:5509061	20241212	MGI			PMID:34931339
1608344	Mir126a	microRNA 126a	gene	MP:0001874	acanthosis		IAGP		N	RGD:5509061	20241212	MGI			PMID:34931339
1608344	Mir126a	microRNA 126a	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20241212	MGI			PMID:34931339
1608344	Mir126a	microRNA 126a	gene	MP:0008086	increased T-helper 1 cell number		IAGP		N	RGD:5509061	20241212	MGI			PMID:34931339
1608344	Mir126a	microRNA 126a	gene	MP:0008091	decreased T-helper 2 cell number		IAGP		N	RGD:5509061	20241212	MGI			PMID:34931339
1608344	Mir126a	microRNA 126a	gene	MP:0010219	increased T-helper 17 cell number		IAGP		N	RGD:5509061	20241212	MGI			PMID:34931339
1608345	Mir10b	microRNA 10b	gene	MP:0000488	abnormal intestinal epithelium morphology		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608345	Mir10b	microRNA 10b	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608345	Mir10b	microRNA 10b	gene	MP:0003304	large intestinal inflammation		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608345	Mir10b	microRNA 10b	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608345	Mir10b	microRNA 10b	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608345	Mir10b	microRNA 10b	gene	MP:0005455	increased susceptibility to weight gain		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608345	Mir10b	microRNA 10b	gene	MP:0005658	increased susceptibility to diet-induced obesity		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608345	Mir10b	microRNA 10b	gene	MP:0006001	abnormal intestinal transit time		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608345	Mir10b	microRNA 10b	gene	MP:0009854	impaired gastric peristalsis		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608345	Mir10b	microRNA 10b	gene	MP:0010155	abnormal intestine physiology		IAGP		N	RGD:5509061	20231221	MGI			PMID:37723933
1608347	Mir24-1	microRNA 24-1	gene	MP:0002073	abnormal hair growth		IAGP		N	RGD:5509061	20210805	MGI			PMID:34107258
1608347	Mir24-1	microRNA 24-1	gene	MP:0009583	increased keratinocyte proliferation		IAGP		N	RGD:5509061	20210805	MGI			PMID:34107258
1608348	Mir22	microRNA 22	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190207	MGI			PMID:28314781
1608348	Mir22	microRNA 22	gene	MP:0001544	abnormal cardiovascular system physiology		IEA		N	RGD:5509061	20141003	MGI			
1608348	Mir22	microRNA 22	gene	MP:0001625	cardiac hypertrophy		IAGP		N	RGD:5509061	20141016	MGI			PMID:23524588
1608348	Mir22	microRNA 22	gene	MP:0001783	decreased white adipose tissue amount		IAGP		N	RGD:5509061	20190207	MGI			PMID:28314781
1608348	Mir22	microRNA 22	gene	MP:0002702	decreased circulating free fatty acids level		IAGP		N	RGD:5509061	20190207	MGI			PMID:28314781
1608348	Mir22	microRNA 22	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20141016	MGI			PMID:23524588
1608348	Mir22	microRNA 22	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20141016	MGI			PMID:23524588
1608348	Mir22	microRNA 22	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20141016	MGI			PMID:23524588
1608348	Mir22	microRNA 22	gene	MP:0005140	decreased cardiac muscle contractility		IEA		N	RGD:5509061	20141003	MGI			
1608348	Mir22	microRNA 22	gene	MP:0005668	decreased circulating leptin level		IAGP		N	RGD:5509061	20190207	MGI			PMID:28314781
1608348	Mir22	microRNA 22	gene	MP:0006138	congestive heart failure		IEA		N	RGD:5509061	20141003	MGI			
1608348	Mir22	microRNA 22	gene	MP:0008022	dilated heart ventricle		IEA		N	RGD:5509061	20141003	MGI			
1608348	Mir22	microRNA 22	gene	MP:0008873	increased physiological sensitivity to xenobiotic		IEA		N	RGD:5509061	20141003	MGI			
1608348	Mir22	microRNA 22	gene	MP:0009133	decreased white fat cell size		IAGP		N	RGD:5509061	20190207	MGI			PMID:28314781
1608348	Mir22	microRNA 22	gene	MP:0014171	increased fatty acid oxidation		IAGP		N	RGD:5509061	20190207	MGI			PMID:28314781
1608348	Mir22	microRNA 22	gene	MP:0020135	abnormal heart ventricle wall thickness		IAGP		N	RGD:5509061	20141016	MGI			PMID:23524588
1608349	Mir21a	microRNA 21a	gene	MP:0000249	abnormal blood vessel physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23527070
1608349	Mir21a	microRNA 21a	gene	MP:0002024	increased T cell derived lymphoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832755
1608349	Mir21a	microRNA 21a	gene	MP:0002048	increased lung adenoma incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832755
1608349	Mir21a	microRNA 21a	gene	MP:0002052	decreased tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832755
1608349	Mir21a	microRNA 21a	gene	MP:0002833	increased heart weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:20978354
1608349	Mir21a	microRNA 21a	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21849676
1608349	Mir21a	microRNA 21a	gene	MP:0003447	decreased tumor growth/size		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832755
1608349	Mir21a	microRNA 21a	gene	MP:0003907	decreased aorta elastin content		IAGP		N	RGD:5509061	20141003	MGI			PMID:23527070
1608349	Mir21a	microRNA 21a	gene	MP:0004042	decreased susceptibility to kidney reperfusion injury		IAGP		N	RGD:5509061	20141003	MGI			PMID:22344686
1608349	Mir21a	microRNA 21a	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646541
1608349	Mir21a	microRNA 21a	gene	MP:0004876	decreased mean systemic arterial blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23527070
1608349	Mir21a	microRNA 21a	gene	MP:0005501	abnormal skin physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646541
1608349	Mir21a	microRNA 21a	gene	MP:0005591	decreased vasodilation		IAGP		N	RGD:5509061	20141003	MGI			PMID:23527070
1608349	Mir21a	microRNA 21a	gene	MP:0005596	increased susceptibility to type I hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21849676
1608349	Mir21a	microRNA 21a	gene	MP:0005617	increased susceptibility to type IV hypersensitivity reaction		IAGP		N	RGD:5509061	20141003	MGI			PMID:21849676
1608349	Mir21a	microRNA 21a	gene	MP:0006263	decreased systemic arterial diastolic blood pressure		IAGP		N	RGD:5509061	20141003	MGI			PMID:23527070
1608349	Mir21a	microRNA 21a	gene	MP:0008566	increased interferon-gamma secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21849676
1608349	Mir21a	microRNA 21a	gene	MP:0008663	increased interleukin-12 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21849676
1608349	Mir21a	microRNA 21a	gene	MP:0008700	decreased interleukin-4 secretion		IAGP		N	RGD:5509061	20141003	MGI			PMID:21849676
1608349	Mir21a	microRNA 21a	gene	MP:0008713	abnormal cytokine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21849676
1608349	Mir21a	microRNA 21a	gene	MP:0008750	abnormal interferon level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21849676
1608349	Mir21a	microRNA 21a	gene	MP:0008751	abnormal interleukin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:21849676
1608349	Mir21a	microRNA 21a	gene	MP:0008874	decreased physiological sensitivity to xenobiotic		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646541
1608349	Mir21a	microRNA 21a	gene	MP:0010267	decreased lung tumor incidence		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832755
1608349	Mir21a	microRNA 21a	gene	MP:0010468	abnormal thoracic aorta morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23527070
1608349	Mir21a	microRNA 21a	gene	MP:0010639	abnormal tumor pathology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21646541
1608349	Mir21a	microRNA 21a	gene	MP:0010945	lung epithelium hyperplasia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20832755
1608349	Mir21a	microRNA 21a	gene	MP:0011640	abnormal aorta collagen fibril morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:23527070
1608351	Mir18	microRNA 18	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20150924	MGI			PMID:26029871
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20200310	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000470	abnormal stomach morphology		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24284070
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000820	abnormal choroid plexus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000827	dilated third ventricle		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0000917	obstructive hydrocephaly		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0001850	increased susceptibility to otitis media		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0001866	nasal inflammation		IAGP		N	RGD:5509061	20171005	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0001917	intraventricular hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0002691	small stomach		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0002958	cerebral aqueductal stenosis		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0010152	abnormal brain ependyma morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0011050	abnormal respiratory motile cilium morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0011056	abnormal brain ependyma motile cilium morphology		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0011057	absent brain ependyma motile cilia		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0011069	abnormal brain ependyma motile cilium physiology		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0012676	dilated brain ventricle		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0013907	abnormal cerebrospinal fluid flow		IAGP		N	RGD:5509061	20170112	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0014402	abnormal Reissner's fiber morphology		IAGP		N	RGD:5509061	20240321	MGI			PMID:27445138
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0030113	maxillary sinus inflammation		IAGP		N	RGD:5509061	20171005	MGI			PMID:21746835
1608439	Ulk4	unc-51-like kinase 4	gene	MP:0030964	decreased brain ependyma motile cilium length		IAGP		N	RGD:5509061	20190725	MGI			PMID:21746835
1608452	Rnf169	ring finger protein 169	gene	MP:0000063	decreased bone mineral density		IEA		N	RGD:5509061	20141003	MGI			
1608452	Rnf169	ring finger protein 169	gene	MP:0000220	increased monocyte cell number		IEA		N	RGD:5509061	20160804	MGI			
1608452	Rnf169	ring finger protein 169	gene	MP:0002702	decreased circulating free fatty acids level		IEA		N	RGD:5509061	20160804	MGI			
1608452	Rnf169	ring finger protein 169	gene	MP:0002896	abnormal bone mineralization		IEA		N	RGD:5509061	20141003	MGI			
1608745	2700054A10Rik	RIKEN cDNA 2700054A10 gene	gene	MP:0001293	anophthalmia		IEA		N	RGD:5509061	20181227	MGI			
1608745	2700054A10Rik	RIKEN cDNA 2700054A10 gene	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20230601	MGI			
1608745	2700054A10Rik	RIKEN cDNA 2700054A10 gene	gene	MP:0001566	increased circulating phosphate level		IEA		N	RGD:5509061	20240523	MGI			
1608745	2700054A10Rik	RIKEN cDNA 2700054A10 gene	gene	MP:0002092	abnormal eye morphology		IEA		N	RGD:5509061	20181227	MGI			
1608842	1700052I22Rik	RIKEN cDNA 1700052I22 gene	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20250605	MGI			PMID:39667612
1608842	1700052I22Rik	RIKEN cDNA 1700052I22 gene	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20250605	MGI			PMID:39667612
1608842	1700052I22Rik	RIKEN cDNA 1700052I22 gene	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39667612
1608842	1700052I22Rik	RIKEN cDNA 1700052I22 gene	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20250605	MGI			PMID:39667612
1608842	1700052I22Rik	RIKEN cDNA 1700052I22 gene	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20250605	MGI			PMID:39667612
1608842	1700052I22Rik	RIKEN cDNA 1700052I22 gene	gene	MP:0009230	abnormal sperm head morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39667612
1608842	1700052I22Rik	RIKEN cDNA 1700052I22 gene	gene	MP:0011750	abnormal seminiferous tubule epithelium morphology		IAGP		N	RGD:5509061	20250605	MGI			PMID:39667612
1608842	1700052I22Rik	RIKEN cDNA 1700052I22 gene	gene	MP:0014634	decreased round spermatid number		IAGP		N	RGD:5509061	20250605	MGI			PMID:39667612
1608842	1700052I22Rik	RIKEN cDNA 1700052I22 gene	gene	MP:0014636	decreased elongated spermatid number		IAGP		N	RGD:5509061	20250605	MGI			PMID:39667612
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0001858	intestinal inflammation		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0003009	abnormal cytokine secretion		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0003292	melena		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0003674	oxidative stress		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0005036	diarrhea		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0005290	decreased oxygen consumption		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0006035	abnormal mitochondrial morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0008537	increased susceptibility to induced colitis		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0010956	abnormal mitochondrial ATP synthesis coupled electron transport		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0010959	abnormal oxidative phosphorylation		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0011631	decreased mitochondrial size		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0011632	dilated mitochondrion		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0011635	abnormal mitochondrial crista morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0011637	abnormal mitochondrial matrix morphology		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608864	Hoxa11os	homeobox A11, opposite strand	gene	MP:0011639	decreased mitochondrial DNA content		IAGP		N	RGD:5509061	20241212	MGI			PMID:37494932
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0001147	small testis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0002216	abnormal seminiferous tubule morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0006362	abnormal male germ cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0008898	abnormal acrosome morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0009231	detached acrosome		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0009238	coiled sperm flagellum		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0009376	abnormal manchette morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0009377	ectopic manchette		IAGP		N	RGD:5509061	20220331	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0009831	abnormal sperm midpiece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0009833	absent sperm mitochondrial sheath		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0009836	abnormal sperm principal piece morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0009839	multiflagellated sperm		IAGP		N	RGD:5509061	20141003	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0031372	abnormal sperm individualization		IAGP		N	RGD:5509061	20220331	MGI			PMID:22764053
1608928	Dpy19l2	dpy-19 like 2	gene	MP:0031386	elongated manchette		IAGP		N	RGD:5509061	20220428	MGI			PMID:22764053
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0000913	abnormal brain development		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0001006	abnormal retina cone cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0001513	limb grasping		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0001732	postnatal growth retardation		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0002761	abnormal hippocampal mossy fiber morphology		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0003203	increased neuron apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0004022	abnormal cone electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0006072	abnormal retina apoptosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0008446	decreased retina cone cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0009938	abnormal hippocampus granule cell morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0011086	postnatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:21857657
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1608991	Mir124a-1hg	Mir124-1 host gene (non-protein coding)	gene	MP:0011091	prenatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230427	MGI			PMID:35868558
1609124	Gata3un	Gata3 upstream neighbor	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0001399	hyperactivity		IEA		N	RGD:5509061	20210128	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0001473	reduced long-term potentiation		IAGP		N	RGD:5509061	20260723	MGI			PMID:38985877
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20250508	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0002912	abnormal excitatory postsynaptic potential		IAGP		N	RGD:5509061	20260723	MGI			PMID:38985877
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0003019	increased circulating chloride level		IEA		N	RGD:5509061	20211021	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20160421	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0004924	abnormal behavior		IEA		N	RGD:5509061	20220519	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0005343	increased circulating aspartate transaminase level		IEA		N	RGD:5509061	20211021	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0005568	increased circulating total protein level		IEA		N	RGD:5509061	20210128	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0005627	increased circulating potassium level		IEA		N	RGD:5509061	20210128	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20210128	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0010124	decreased bone mineral content		IEA		N	RGD:5509061	20210128	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0011269	increased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260723	MGI			PMID:38985877
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0011396	abnormal sleep behavior		IEA		N	RGD:5509061	20260402	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0014378	increased excitatory postsynaptic current frequency		IAGP		N	RGD:5509061	20260723	MGI			PMID:38985877
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0020870	decreased thigmotaxis		IEA		N	RGD:5509061	20220519	MGI			
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0031334	increased inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260723	MGI			PMID:38985877
1609478	Ajap1	adherens junction associated protein 1	gene	MP:0031753	increased inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20260813	MGI			PMID:38985877
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190919	MGI			PMID:27783597
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0003872	absent heart right ventricle		IAGP		N	RGD:5509061	20190919	MGI			PMID:27783597
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0003984	embryonic growth retardation		IAGP		N	RGD:5509061	20190919	MGI			PMID:27783597
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0005312	pericardial effusion		IAGP		N	RGD:5509061	20190919	MGI			PMID:27783597
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0010432	common ventricle		IAGP		N	RGD:5509061	20190919	MGI			PMID:27783597
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0011089	perinatal lethality, complete penetrance		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0011092	embryonic lethality, complete penetrance		IAGP		N	RGD:5509061	20190919	MGI			PMID:27783597
1609552	Hand2os1	Hand2, opposite strand 1	gene	MP:0012167	abnormal epigenetic regulation of gene expression		IAGP		N	RGD:5509061	20190919	MGI			PMID:27783597
1609618	Btnl6	butyrophilin-like 6	gene	MP:0008359	decreased CD4-positive, gamma-delta intraepithelial T cell number		IAGP		N	RGD:5509061	20231109	MGI			PMID:32724083
1609759	Pldi	polymorphic derived intron containing	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733073
1609759	Pldi	polymorphic derived intron containing	gene	MP:0004852	decreased testis weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:19733073
1609826	1600029I14Rik	RIKEN cDNA 1600029I14 gene	gene	MP:0002135	abnormal kidney morphology		IEA		N	RGD:5509061	20200514	MGI			
1609826	1600029I14Rik	RIKEN cDNA 1600029I14 gene	gene	MP:0004930	small epididymis		IEA		N	RGD:5509061	20200514	MGI			
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0000490	abnormal crypts of Lieberkuhn morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0003119	abnormal digestive system development		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0004502	decreased incidence of tumors by chemical induction		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0008108	abnormal small intestinal villus morphology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0008882	abnormal enterocyte physiology		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0008883	abnormal enterocyte proliferation		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0012434	decreased intestinal adenoma incidence		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1609846	Gata6os	GATA binding protein 6, opposite strand	gene	MP:0012734	abnormal response to radiation		IAGP		N	RGD:5509061	20191107	MGI			PMID:30224759
1609892	Fnip2	folliculin interacting protein 2	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1609892	Fnip2	folliculin interacting protein 2	gene	MP:0003068	enlarged kidney		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1609892	Fnip2	folliculin interacting protein 2	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1609892	Fnip2	folliculin interacting protein 2	gene	MP:0008528	polycystic kidney		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1609892	Fnip2	folliculin interacting protein 2	gene	MP:0008810	increased circulating iron level		IEA		N	RGD:5509061	20210128	MGI			
1609892	Fnip2	folliculin interacting protein 2	gene	MP:0010294	increased kidney tumor incidence		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1609892	Fnip2	folliculin interacting protein 2	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20170525	MGI			PMID:25775561
1609948	Sros1	non-coding RNA suppressor of Stat1	gene	MP:0002411	decreased susceptibility to bacterial infection		IAGP		N	RGD:5509061	20210701	MGI			PMID:31740800
1609948	Sros1	non-coding RNA suppressor of Stat1	gene	MP:0009789	decreased susceptibility to bacterial infection induced morbidity/mortality		IAGP		N	RGD:5509061	20210701	MGI			PMID:31740800
1609948	Sros1	non-coding RNA suppressor of Stat1	gene	MP:0010209	abnormal circulating chemokine level		IAGP		N	RGD:5509061	20210701	MGI			PMID:31740800
1609948	Sros1	non-coding RNA suppressor of Stat1	gene	MP:0031220	increased circulating CXCL10 level		IAGP		N	RGD:5509061	20210701	MGI			PMID:31740800
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0001614	abnormal blood vessel morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0002625	heart left ventricle hypertrophy		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0003141	cardiac fibrosis		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0003393	decreased cardiac output		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0005329	abnormal myocardium layer morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0005333	decreased heart rate		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0006431	abnormal fibrocartilage morphology		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610154	Platr4	pluripotency associated transcript 4	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20221215	MGI			PMID:36347239
1610182	Redrum	Redrum, erythroid developmental long intergenic non-protein coding transcript	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20200806	MGI			PMID:29237115
1610387	Atcayos	ataxia, cerebellar, Cayman type, opposite strand	gene	MP:0003916	decreased heart left ventricle weight		IAGP		N	RGD:5509061	20200402	MGI			PMID:31784461
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0000753	paralysis		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0000955	abnormal spinal cord morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0001402	decreased locomotor activity		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0001661	extended life span		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0002229	neurodegeneration		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0002574	increased vertical activity		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0002757	decreased vertical activity		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0002882	abnormal neuron morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0003244	loss of dopaminergic neurons		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0003354	astrocytosis		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0004191	neuronal intranuclear inclusions		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0005156	bradykinesia		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20180201	MGI			PMID:12084935
1610393	2310039L15Rik	RIKEN cDNA 2310039L15 gene	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20241114	MGI			PMID:31237944
1610443	Ccdc180	coiled-coil domain containing 180	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20240523	MGI			
1610443	Ccdc180	coiled-coil domain containing 180	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20240523	MGI			
1610443	Ccdc180	coiled-coil domain containing 180	gene	MP:0005543	decreased cornea thickness		IEA		N	RGD:5509061	20240523	MGI			
1610450	Trim67	tripartite motif-containing 67	gene	MP:0000781	decreased corpus callosum size		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0000783	abnormal forebrain morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0000807	abnormal hippocampus morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0001489	decreased startle reflex		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0004102	abnormal dorsal striatum morphology		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0008222	decreased hippocampal commissure size		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0008283	small hippocampus		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0009142	decreased prepulse inhibition		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0010053	decreased grip strength		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0012307	impaired spatial learning		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0012462	decreased brain internal capsule size		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0012480	decreased amygdala size		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0013908	small lateral ventricles		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0014114	abnormal cognition		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0014115	cognitive inflexibility		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0020395	abnormal response to social novelty		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0020527	small thalamus		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610450	Trim67	tripartite motif-containing 67	gene	MP:0020554	decreased stria medullaris size		IAGP		N	RGD:5509061	20181220	MGI			PMID:29911180
1610489	Leat1	lncRNA Efnb2 associated transcript 1	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200430	MGI			PMID:31830612
1610489	Leat1	lncRNA Efnb2 associated transcript 1	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200430	MGI			PMID:31830612
1610489	Leat1	lncRNA Efnb2 associated transcript 1	gene	MP:0003550	short perineum		IAGP		N	RGD:5509061	20200430	MGI			PMID:31830612
1610489	Leat1	lncRNA Efnb2 associated transcript 1	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20200430	MGI			PMID:31830612
1610800	1700069L16Rik	RIKEN cDNA 1700069L16 gene	gene	MP:0000598	abnormal liver morphology		IEA		N	RGD:5509061	20220811	MGI			
1610800	1700069L16Rik	RIKEN cDNA 1700069L16 gene	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220811	MGI			
1610800	1700069L16Rik	RIKEN cDNA 1700069L16 gene	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220811	MGI			
1610866	Krt28	keratin 28	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1610866	Krt28	keratin 28	gene	MP:0002059	abnormal seminal vesicle morphology		IEA		N	RGD:5509061	20210520	MGI			
1610866	Krt28	keratin 28	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1610875	Mir205hg	Mir205 host gene	gene	MP:0000706	small thymus		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
1610875	Mir205hg	Mir205 host gene	gene	MP:0000715	decreased thymocyte number		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
1610875	Mir205hg	Mir205 host gene	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
1610875	Mir205hg	Mir205 host gene	gene	MP:0001265	decreased body size		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
1610875	Mir205hg	Mir205 host gene	gene	MP:0001823	thymus hypoplasia		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
1610875	Mir205hg	Mir205 host gene	gene	MP:0004956	decreased thymus weight		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
1610875	Mir205hg	Mir205 host gene	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
1610875	Mir205hg	Mir205 host gene	gene	MP:0005136	decreased growth hormone level		IAGP		N	RGD:5509061	20190919	MGI			PMID:30982661
1610900	Fcor	Foxo1 corepressor	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
1610900	Fcor	Foxo1 corepressor	gene	MP:0005289	increased oxygen consumption		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
1610900	Fcor	Foxo1 corepressor	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
1610900	Fcor	Foxo1 corepressor	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
1610900	Fcor	Foxo1 corepressor	gene	MP:0009118	increased white fat cell size		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
1610900	Fcor	Foxo1 corepressor	gene	MP:0010379	decreased respiratory quotient		IAGP		N	RGD:5509061	20141003	MGI			PMID:22510882
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0000627	abnormal mammary gland morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0000628	abnormal mammary gland development		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0000662	abnormal branching of the mammary ductal tree		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0001882	abnormal lactation		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0003111	abnormal cell nucleus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:21444682
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0003718	maternal effect		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0009504	abnormal mammary gland epithelium morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0009506	abnormal mammary gland alveolus morphology		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0010174	decreased mammary gland epithelial cell proliferation		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610909	Neat1	nuclear paraspeckle assembly transcript 1 (non-protein coding)	gene	MP:0011940	decreased food intake		IAGP		N	RGD:5509061	20160211	MGI			PMID:25316907
1610965	Gpr62	G protein-coupled receptor 62	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:28912303
1610968	Ptprh	protein tyrosine phosphatase receptor type H	gene	MP:0002053	decreased incidence of induced tumors		IAGP		N	RGD:5509061	20141003	MGI			PMID:19170756
1611166	Mir142hg	Mir142 host gene (non-protein coding)	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141009	MGI			PMID:24352241
1611166	Mir142hg	Mir142 host gene (non-protein coding)	gene	MP:0000691	enlarged spleen		IAGP		N	RGD:5509061	20141009	MGI			PMID:24352241
1611166	Mir142hg	Mir142 host gene (non-protein coding)	gene	MP:0002123	abnormal definitive hematopoiesis		IAGP		N	RGD:5509061	20141009	MGI			PMID:24352241
1611166	Mir142hg	Mir142 host gene (non-protein coding)	gene	MP:0005461	abnormal dendritic cell morphology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24352241
1611166	Mir142hg	Mir142 host gene (non-protein coding)	gene	MP:0008115	abnormal dendritic cell differentiation		IAGP		N	RGD:5509061	20141009	MGI			PMID:24352241
1611166	Mir142hg	Mir142 host gene (non-protein coding)	gene	MP:0008126	increased dendritic cell number		IAGP		N	RGD:5509061	20141009	MGI			PMID:24352241
1611166	Mir142hg	Mir142 host gene (non-protein coding)	gene	MP:0008127	decreased dendritic cell number		IAGP		N	RGD:5509061	20141009	MGI			PMID:24352241
1611166	Mir142hg	Mir142 host gene (non-protein coding)	gene	MP:0009278	abnormal bone marrow cell physiology		IAGP		N	RGD:5509061	20141009	MGI			PMID:24352241
1611244	Hdnr	Hand2 downstream lncRNA	gene	MP:0003916	decreased heart left ventricle weight		IAGP		N	RGD:5509061	20200402	MGI			PMID:31784461
1611244	Hdnr	Hand2 downstream lncRNA	gene	MP:0005599	increased cardiac muscle contractility		IAGP		N	RGD:5509061	20200402	MGI			PMID:31784461
1611244	Hdnr	Hand2 downstream lncRNA	gene	MP:0005629	abnormal lung weight		IAGP		N	RGD:5509061	20200402	MGI			PMID:31784461
1611412	Snhg12	small nucleolar RNA host gene 12	gene	MP:0001458	abnormal object recognition memory		IAGP		N	RGD:5509061	20260514	MGI			PMID:35417709
1611412	Snhg12	small nucleolar RNA host gene 12	gene	MP:0003461	abnormal response to novel object		IAGP		N	RGD:5509061	20260514	MGI			PMID:35417709
1611412	Snhg12	small nucleolar RNA host gene 12	gene	MP:0008414	abnormal spatial reference memory		IAGP		N	RGD:5509061	20260514	MGI			PMID:35417709
1611412	Snhg12	small nucleolar RNA host gene 12	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20260514	MGI			PMID:35417709
1611412	Snhg12	small nucleolar RNA host gene 12	gene	MP:0014179	abnormal blood-retina barrier function		IAGP		N	RGD:5509061	20260514	MGI			PMID:35417709
1611412	Snhg12	small nucleolar RNA host gene 12	gene	MP:0031252	abnormal physiological response to hypoxia		IAGP		N	RGD:5509061	20260514	MGI			PMID:35417709
1611412	Snhg12	small nucleolar RNA host gene 12	gene	MP:0031384	impaired blood-brain barrier function		IAGP		N	RGD:5509061	20260514	MGI			PMID:35417709
1611458	Ildr2	immunoglobulin-like domain containing receptor 2	gene	MP:0001559	hyperglycemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654634
1611458	Ildr2	immunoglobulin-like domain containing receptor 2	gene	MP:0002727	decreased circulating insulin level		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654634
1611458	Ildr2	immunoglobulin-like domain containing receptor 2	gene	MP:0003339	decreased pancreatic beta cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654634
1611458	Ildr2	immunoglobulin-like domain containing receptor 2	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654634
1611458	Ildr2	immunoglobulin-like domain containing receptor 2	gene	MP:0009114	decreased pancreatic beta cell mass		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654634
1611458	Ildr2	immunoglobulin-like domain containing receptor 2	gene	MP:0009175	abnormal pancreatic beta cell differentiation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18654634
1611478	Baiap3	BAI1-associated protein 3	gene	MP:0001363	increased anxiety-related response		IAGP		N	RGD:5509061	20151001	MGI			PMID:23698091
1611478	Baiap3	BAI1-associated protein 3	gene	MP:0002797	increased thigmotaxis		IAGP		N	RGD:5509061	20151001	MGI			PMID:23698091
1611478	Baiap3	BAI1-associated protein 3	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20151001	MGI			PMID:23698091
1611478	Baiap3	BAI1-associated protein 3	gene	MP:0003107	abnormal response to novelty		IAGP		N	RGD:5509061	20151001	MGI			PMID:23698091
1611478	Baiap3	BAI1-associated protein 3	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20151001	MGI			PMID:23698091
1611478	Baiap3	BAI1-associated protein 3	gene	MP:0009745	abnormal behavioral response to xenobiotic		IAGP		N	RGD:5509061	20151001	MGI			PMID:23698091
1611478	Baiap3	BAI1-associated protein 3	gene	MP:0014385	decreased miniature inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20240404	MGI			PMID:23698091
1611478	Baiap3	BAI1-associated protein 3	gene	MP:0031332	abnormal inhibitory postsynaptic current amplitude		IAGP		N	RGD:5509061	20260813	MGI			PMID:23698091
1611478	Baiap3	BAI1-associated protein 3	gene	MP:0031751	abnormal inhibitory postsynaptic current frequency		IAGP		N	RGD:5509061	20260813	MGI			PMID:23698091
1611507	Lcn6	lipocalin 6	gene	MP:0004231	abnormal calcium ion homeostasis		IAGP		N	RGD:5509061	20180329	MGI			PMID:29045572
1611507	Lcn6	lipocalin 6	gene	MP:0004543	abnormal sperm physiology		IAGP		N	RGD:5509061	20180329	MGI			PMID:29045572
1611507	Lcn6	lipocalin 6	gene	MP:0013288	premature acrosome reaction		IAGP		N	RGD:5509061	20180329	MGI			PMID:29045572
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:16033881
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0001777	abnormal body temperature homeostasis		IAGP		N	RGD:5509061	20180201	MGI			PMID:25176149
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0001923	reduced female fertility		IAGP		N	RGD:5509061	20200123	MGI			PMID:31285329
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20200123	MGI			PMID:31285329
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20180201	MGI			PMID:16033881
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20180201	MGI			PMID:19630976
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0002175	decreased brain weight		IAGP		N	RGD:5509061	20180201	MGI			PMID:16033881
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0002773	decreased circulating luteinizing hormone level		IAGP		N	RGD:5509061	20200123	MGI			PMID:31285329
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0002803	abnormal operant conditioning behavior		IAGP		N	RGD:5509061	20180201	MGI			PMID:26869263
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20200123	MGI			PMID:31285329
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0003638	abnormal response/metabolism to endogenous compounds		IAGP		N	RGD:5509061	20180201	MGI			PMID:25176149
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0003661	abnormal locus ceruleus morphology		IAGP		N	RGD:5509061	20180201	MGI			PMID:16033881
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0004008	abnormal GABA-mediated receptor currents		IAGP		N	RGD:5509061	20180201	MGI			PMID:26869263
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0005121	decreased circulating prolactin level		IAGP		N	RGD:5509061	20200123	MGI			PMID:31285329
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0005402	abnormal action potential		IAGP		N	RGD:5509061	20200123	MGI			PMID:31285329
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20180201	MGI			PMID:16033881
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0005643	decreased dopamine level		IAGP		N	RGD:5509061	20180201	MGI			PMID:19630976
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0005665	increased circulating noradrenaline level		IAGP		N	RGD:5509061	20180201	MGI			PMID:19630976
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0009006	prolonged estrous cycle		IAGP		N	RGD:5509061	20200123	MGI			PMID:31285329
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0009011	prolonged diestrus		IAGP		N	RGD:5509061	20200123	MGI			PMID:31285329
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0009016	abnormal estrus		IAGP		N	RGD:5509061	20200123	MGI			PMID:31285329
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0010069	increased serotonin level		IAGP		N	RGD:5509061	20180920	MGI			PMID:19630976
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0012575	increased noradrenaline level		IAGP		N	RGD:5509061	20180920	MGI			PMID:19630976
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0020543	decreased substantia nigra size		IAGP		N	RGD:5509061	20180301	MGI			PMID:16033881
1611742	7630403G23Rik	RIKEN cDNA 7630403G23 gene	gene	MP:0030586	impaired behavioral response to amphetamine		IAGP		N	RGD:5509061	20250424	MGI			PMID:32778904
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000495	abnormal colon morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000627	abnormal mammary gland morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0000759	abnormal skeletal muscle morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0001925	male infertility		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0001926	female infertility		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0002100	abnormal tooth morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0002581	abnormal ileum morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0003271	abnormal duodenum morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0004002	abnormal jejunum morphology		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20230601	MGI			
1611791	Fam227b	family with sequence similarity 227, member B	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20240523	MGI			
1611801	4930463O16Rik	RIKEN cDNA 4930463O16 gene	gene	MP:0002674	abnormal sperm motility		IAGP		N	RGD:5509061	20221124	MGI			PMID:34277642
1611801	4930463O16Rik	RIKEN cDNA 4930463O16 gene	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20221124	MGI			PMID:34277642
1611801	4930463O16Rik	RIKEN cDNA 4930463O16 gene	gene	MP:0008892	abnormal sperm flagellum morphology		IAGP		N	RGD:5509061	20221124	MGI			PMID:34277642
1611801	4930463O16Rik	RIKEN cDNA 4930463O16 gene	gene	MP:0031426	increased sperm motility		IAGP		N	RGD:5509061	20221124	MGI			PMID:34277642
1611801	4930463O16Rik	RIKEN cDNA 4930463O16 gene	gene	MP:0031427	increased sperm progressive motility		IAGP		N	RGD:5509061	20221124	MGI			PMID:34277642
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0000218	increased leukocyte cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0000703	abnormal thymus morphology		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0000709	enlarged thymus		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0001402	decreased locomotor activity		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0001577	anemia		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0002429	abnormal blood cell morphology/development		IAGP		N	RGD:5509061	20141003	MGI			PMID:20233966
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0002631	abnormal epididymis morphology		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0002797	increased thigmotaxis		IEA		N	RGD:5509061	20260402	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0004931	enlarged epididymis		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0005084	abnormal gallbladder morphology		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0009342	enlarged gallbladder		IEA		N	RGD:5509061	20220519	MGI			
1611829	Lrrc17	leucine rich repeat containing 17	gene	MP:0020421	increased freezing behavior		IEA		N	RGD:5509061	20220519	MGI			
1611847	Dino	damage induced long noncoding RNA	gene	MP:0003010	decreased mortality induced by ionizing radiation		IAGP		N	RGD:5509061	20220922	MGI			PMID:27668660
1611847	Dino	damage induced long noncoding RNA	gene	MP:0003207	decreased cellular sensitivity to gamma-irradiation		IAGP		N	RGD:5509061	20220922	MGI			PMID:27668660
1611847	Dino	damage induced long noncoding RNA	gene	MP:0008009	delayed cellular replicative senescence		IAGP		N	RGD:5509061	20220922	MGI			PMID:27668660
1611847	Dino	damage induced long noncoding RNA	gene	MP:0014042	decreased cellular sensitivity to DNA damaging agent induced cell death		IAGP		N	RGD:5509061	20220922	MGI			PMID:27668660
1611867	Ptchd4	patched domain containing 4	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230119	MGI			
1611867	Ptchd4	patched domain containing 4	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230119	MGI			
1611867	Ptchd4	patched domain containing 4	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230119	MGI			
1611867	Ptchd4	patched domain containing 4	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230119	MGI			
1611867	Ptchd4	patched domain containing 4	gene	MP:0011044	increased lung elastance		IEA		N	RGD:5509061	20231207	MGI			
1611912	Lelp1	late cornified envelope-like proline-rich 1	gene	MP:0005389	reproductive system phenotype		IAGP		N	RGD:5509061	20201022	MGI			PMID:32588039
1611959	Ms4a12	membrane-spanning 4-domains, subfamily A, member 12	gene	MP:0000702	enlarged lymph nodes		IEA		N	RGD:5509061	20210520	MGI			
1611959	Ms4a12	membrane-spanning 4-domains, subfamily A, member 12	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20210520	MGI			
1611959	Ms4a12	membrane-spanning 4-domains, subfamily A, member 12	gene	MP:0002941	increased circulating alanine transaminase level		IEA		N	RGD:5509061	20220519	MGI			
1612156	Lhx1os	LIM homeobox 1, opposite strand	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1612159	2500002B13Rik	RIKEN cDNA 2500002B13 gene	gene	MP:0004215	abnormal myocardial fiber physiology		IAGP		N	RGD:5509061	20211104	MGI			PMID:33953175
1612159	2500002B13Rik	RIKEN cDNA 2500002B13 gene	gene	MP:0004485	increased response of heart to induced stress		IAGP		N	RGD:5509061	20211104	MGI			PMID:33953175
1612159	2500002B13Rik	RIKEN cDNA 2500002B13 gene	gene	MP:0004486	decreased response of heart to induced stress		IAGP		N	RGD:5509061	20211104	MGI			PMID:33953175
1612159	2500002B13Rik	RIKEN cDNA 2500002B13 gene	gene	MP:0006036	abnormal mitochondrial physiology		IAGP		N	RGD:5509061	20211104	MGI			PMID:33953175
1612159	2500002B13Rik	RIKEN cDNA 2500002B13 gene	gene	MP:0011628	increased mitochondrial number		IAGP		N	RGD:5509061	20211104	MGI			PMID:33953175
1612204	Mpped2	metallophosphoesterase domain containing 2	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1612204	Mpped2	metallophosphoesterase domain containing 2	gene	MP:0001488	increased startle reflex		IEA		N	RGD:5509061	20240523	MGI			
1612289	Evx1os	even skipped homeotic gene 1, opposite strand	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1612333	Pantr2	POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2	gene	MP:0000861	disorganized barrel cortex		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1612333	Pantr2	POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1612333	Pantr2	POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2	gene	MP:0003989	abnormal barrel cortex morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1612333	Pantr2	POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2	gene	MP:0004274	abnormal embryonic/fetal subventricular zone morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1612333	Pantr2	POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2	gene	MP:0008947	increased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1612333	Pantr2	POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1612333	Pantr2	POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2	gene	MP:0020069	decreased neocortex size		IAGP		N	RGD:5509061	20141003	MGI			PMID:24381249
1612334	Oip5os1	Opa interacting protein 5, opposite strand 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20190523	MGI			PMID:29887379
1612334	Oip5os1	Opa interacting protein 5, opposite strand 1	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1612354	Rn7sk	RNA, 7SK, nuclear	gene	MP:0001216	abnormal epidermal layer morphology		IAGP		N	RGD:5509061	20221208	MGI			PMID:34620876
1612354	Rn7sk	RNA, 7SK, nuclear	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20221208	MGI			PMID:34620876
1612360	Nrg2	neuregulin 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340081
1612360	Nrg2	neuregulin 2	gene	MP:0001935	decreased litter size		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340081
1612360	Nrg2	neuregulin 2	gene	MP:0002082	postnatal lethality		IAGP		N	RGD:5509061	20141003	MGI			PMID:15340081
1612412	Map3k15	mitogen-activated protein kinase kinase kinase 15	gene	MP:0000231	hypertension		IAGP		N	RGD:5509061	20151022	MGI			PMID:23250415
1612412	Map3k15	mitogen-activated protein kinase kinase kinase 15	gene	MP:0002136	abnormal kidney physiology		IAGP		N	RGD:5509061	20151022	MGI			PMID:23250415
1612412	Map3k15	mitogen-activated protein kinase kinase kinase 15	gene	MP:0004217	salt-sensitive hypertension		IAGP		N	RGD:5509061	20151022	MGI			PMID:23250415
1612412	Map3k15	mitogen-activated protein kinase kinase kinase 15	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20151022	MGI			PMID:23250415
1612412	Map3k15	mitogen-activated protein kinase kinase kinase 15	gene	MP:0006144	increased systemic arterial systolic blood pressure		IAGP		N	RGD:5509061	20151022	MGI			PMID:23250415
1612419	Cog5	component of oligomeric golgi complex 5	gene	MP:0000266	abnormal heart morphology		IEA		N	RGD:5509061	20230601	MGI			
1612419	Cog5	component of oligomeric golgi complex 5	gene	MP:0000274	enlarged heart		IEA		N	RGD:5509061	20230601	MGI			
1612419	Cog5	component of oligomeric golgi complex 5	gene	MP:0000689	abnormal spleen morphology		IEA		N	RGD:5509061	20230601	MGI			
1612419	Cog5	component of oligomeric golgi complex 5	gene	MP:0000691	enlarged spleen		IEA		N	RGD:5509061	20230601	MGI			
1612419	Cog5	component of oligomeric golgi complex 5	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20230601	MGI			
1612419	Cog5	component of oligomeric golgi complex 5	gene	MP:0002110	abnormal digit morphology		IEA		N	RGD:5509061	20230601	MGI			
1612419	Cog5	component of oligomeric golgi complex 5	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20230601	MGI			
1612419	Cog5	component of oligomeric golgi complex 5	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20240523	MGI			
1612419	Cog5	component of oligomeric golgi complex 5	gene	MP:0013293	embryonic lethality prior to tooth bud stage		IEA		N	RGD:5509061	20240523	MGI			
1612423	Dbx2	developing brain homeobox 2	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20220811	MGI			
1612423	Dbx2	developing brain homeobox 2	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20220407	MGI			PMID:33497014
1612425	Rnf157	ring finger protein 157	gene	MP:0001303	abnormal lens morphology		IEA		N	RGD:5509061	20181227	MGI			
1612425	Rnf157	ring finger protein 157	gene	MP:0001304	cataract		IEA		N	RGD:5509061	20181227	MGI			
1612425	Rnf157	ring finger protein 157	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25342469
1612425	Rnf157	ring finger protein 157	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0001146	abnormal testis morphology		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0001156	abnormal spermatogenesis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20230817	MGI			PMID:35256600
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20230817	MGI			PMID:35256600
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0002686	globozoospermia		IAGP		N	RGD:5509061	20230817	MGI			PMID:35256600
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0002687	oligozoospermia		IAGP		N	RGD:5509061	20230817	MGI			PMID:35256600
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0002780	decreased circulating testosterone level		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20230817	MGI			PMID:35256600
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0014052	increased male germ cell apoptosis		IAGP		N	RGD:5509061	20250410	MGI			PMID:38909026
1612426	Tent5d	terminal nucleotidyltransferase 5D	gene	MP:0020550	multinucleated giant male germ cells		IAGP		N	RGD:5509061	20230817	MGI			PMID:35256600
1612491	Pax1dt	paired box 1 divergent transcript	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240328	MGI			PMID:27986952
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0000267	abnormal heart development		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0002652	thin myocardium		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0002740	heart hypoplasia		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0004564	increased myocardial fiber size		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0005140	decreased cardiac muscle contractility		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0010633	myocardium hypertrophy		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0011101	prenatal lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0011102	embryonic lethality, incomplete penetrance		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0011925	abnormal heart echocardiography feature		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612595	1700021F13Rik	RIKEN cDNA 1700021F13 gene	gene	MP:0031611	decreased fetal cardiomyocyte number		IAGP		N	RGD:5509061	20250410	MGI			PMID:36318802
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0000242	impaired fertilization		IAGP		N	RGD:5509061	20141003	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0001125	abnormal oocyte morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0001131	abnormal ovarian follicle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0001926	female infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0001931	abnormal oogenesis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0003355	decreased ovulation rate		IAGP		N	RGD:5509061	20141003	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0005431	decreased oocyte number		IAGP		N	RGD:5509061	20141003	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0005561	increased mean corpuscular hemoglobin		IEA		N	RGD:5509061	20160804	MGI			
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0005621	abnormal cell physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0009433	polyovular ovarian follicle		IAGP		N	RGD:5509061	20220407	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0011701	decreased cumulus expansion		IAGP		N	RGD:5509061	20141003	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0014445	abnormal spindle assembly in female meiosis		IAGP		N	RGD:5509061	20240509	MGI			PMID:22621333
1612607	Pabpc1l	poly(A) binding protein, cytoplasmic 1-like	gene	MP:0031383	increased secondary ovarian follicle number		IAGP		N	RGD:5509061	20220407	MGI			PMID:22621333
1612622	Rab26os	RAB26, member RAS oncogene family, opposite strand	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20230126	MGI			PMID:29420831
1612790	Vaultrc5	vault RNA component 5	gene	MP:0000208	decreased hematocrit		IAGP		N	RGD:5509061	20241226	MGI			PMID:39209555
1612790	Vaultrc5	vault RNA component 5	gene	MP:0011898	abnormal platelet cell number		IAGP		N	RGD:5509061	20241226	MGI			PMID:39209555
1612971	Flicr	Foxp3 regulating long intergenic noncoding RNA	gene	MP:0004031	insulitis		IAGP		N	RGD:5509061	20170921	MGI			PMID:28396406
1612971	Flicr	Foxp3 regulating long intergenic noncoding RNA	gene	MP:0004804	decreased susceptibility to autoimmune diabetes		IAGP		N	RGD:5509061	20170921	MGI			PMID:28396406
1612991	4930404H24Rik	RIKEN cDNA 4930404H24 gene	gene	MP:0002599	increased mean platelet volume		IEA		N	RGD:5509061	20210128	MGI			
1612991	4930404H24Rik	RIKEN cDNA 4930404H24 gene	gene	MP:0005419	decreased circulating serum albumin level		IEA		N	RGD:5509061	20211021	MGI			
1613143	4833411C07Rik	RIKEN cDNA 4833411C07 gene	gene	MP:0005293	impaired glucose tolerance		IAGP		N	RGD:5509061	20210506	MGI			PMID:32005828
1613143	4833411C07Rik	RIKEN cDNA 4833411C07 gene	gene	MP:0005331	insulin resistance		IAGP		N	RGD:5509061	20210506	MGI			PMID:32005828
1613143	4833411C07Rik	RIKEN cDNA 4833411C07 gene	gene	MP:0005559	increased circulating glucose level		IAGP		N	RGD:5509061	20210506	MGI			PMID:32005828
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20210211	MGI			PMID:32891704
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0001401	jumpy		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0001405	impaired coordination		IAGP		N	RGD:5509061	20210211	MGI			PMID:32891704
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0001441	increased grooming behavior		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0001454	abnormal cued conditioning behavior		IEA		N	RGD:5509061	20210128	MGI			
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0001489	decreased startle reflex		IEA		N	RGD:5509061	20181227	MGI			
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0001496	audiogenic seizures		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0001523	impaired righting response		IAGP		N	RGD:5509061	20210211	MGI			PMID:32891704
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0001525	impaired balance		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0002066	abnormal motor capabilities/coordination/movement		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0002764	short tibia		IEA		N	RGD:5509061	20210128	MGI			
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0002906	increased susceptibility to pharmacologically induced seizures		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0002910	abnormal excitatory postsynaptic currents		IAGP		N	RGD:5509061	20210211	MGI			PMID:32891704
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0002945	abnormal inhibitory postsynaptic currents		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0002966	decreased circulating alkaline phosphatase level		IEA		N	RGD:5509061	20211021	MGI			
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0004753	abnormal miniature excitatory postsynaptic currents		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0004859	abnormal synaptic plasticity		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0005323	dystonia		IAGP		N	RGD:5509061	20210211	MGI			PMID:32891704
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0005424	jerky movement		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0008806	increased circulating amylase level		IEA		N	RGD:5509061	20211021	MGI			
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0008911	induced hyperactivity		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0009538	abnormal synapse morphology		IAGP		N	RGD:5509061	20210211	MGI			PMID:32891704
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0010323	retropulsion		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0011270	decreased excitatory postsynaptic current amplitude		IAGP		N	RGD:5509061	20210211	MGI			PMID:32891704
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0020357	abnormal excitatory synapse morphology		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0020358	abnormal inhibitory synapse morphology		IAGP		N	RGD:5509061	20170309	MGI			PMID:28007585
1613176	Prrt2	proline-rich transmembrane protein 2	gene	MP:0031391	increased locomotor activity		IAGP		N	RGD:5509061	20220421	MGI			PMID:32891704
1613196	Klra15	killer cell lectin-like receptor, subfamily A, member 15	gene	MP:0005070	impaired natural killer cell mediated cytotoxicity		IAGP		N	RGD:5509061	20141003	MGI			PMID:22661698
1613284	Gcnt4	glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase)	gene	MP:0000219	increased neutrophil cell number		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1613284	Gcnt4	glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase)	gene	MP:0000511	abnormal intestinal mucosa morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1613284	Gcnt4	glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase)	gene	MP:0001354	increased aggression towards male mice		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1613284	Gcnt4	glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase)	gene	MP:0002135	abnormal kidney morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1613284	Gcnt4	glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase)	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1613284	Gcnt4	glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase)	gene	MP:0005478	decreased circulating thyroxine level		IAGP		N	RGD:5509061	20141003	MGI			PMID:19349303
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0000111	cleft palate		IAGP		N	RGD:5509061	20200514	MGI			PMID:31600785
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0000285	abnormal heart valve morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0000394	absent hair follicle melanin granules		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0000564	syndactyly		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0000571	interdigital webbing		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0001293	anophthalmia		IAGP		N	RGD:5509061	20200514	MGI			PMID:31600785
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0001297	microphthalmia		IAGP		N	RGD:5509061	20200514	MGI			PMID:31600785
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0001683	absent mesoderm		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0001695	abnormal gastrulation		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20190808	MGI			
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0002075	abnormal coat/hair pigmentation		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0002092	abnormal eye morphology		IAGP		N	RGD:5509061	20200514	MGI			PMID:31600785
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0002339	abnormal lymph node morphology		IEA		N	RGD:5509061	20170105	MGI			
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0002582	disorganized extraembryonic tissue		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0003886	abnormal embryonic epiblast morphology		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0003984	embryonic growth retardation		IEA		N	RGD:5509061	20210520	MGI			
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0003988	disorganized embryonic tissue		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0005072	abnormal hair follicle melanin granule morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0005174	abnormal tail pigmentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:29781574
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0009387	abnormal epidermal pigmentation		IAGP		N	RGD:5509061	20180719	MGI			PMID:29781574
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0009783	abnormal melanoblast morphology		IAGP		N	RGD:5509061	20180719	MGI			PMID:29781574
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0009890	cleft secondary palate		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0011087	neonatal lethality, complete penetrance		IAGP		N	RGD:5509061	20200514	MGI			PMID:31600785
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:18454205
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19922873
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0011096	embryonic lethality between implantation and somite formation, complete penetrance		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20141120	MGI			PMID:24753090
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0011100	preweaning lethality, complete penetrance		IAGP		N	RGD:5509061	20180719	MGI			PMID:29781574
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0011110	preweaning lethality, incomplete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0011186	abnormal visceral endoderm morphology		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0013292	embryonic lethality prior to organogenesis		IEA		N	RGD:5509061	20201231	MGI			
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0014134	abnormal embryo morphology		IAGP		N	RGD:5509061	20170105	MGI			PMID:27297885
1613350	Adamts9	ADAM metallopeptidase with thrombospondin type 1 motif 9	gene	MP:0030911	increased melanoblast apoptosis		IAGP		N	RGD:5509061	20190411	MGI			PMID:29781574
1613420	6430503K07Rik	RIKEN cDNA 6430503K07 gene	gene	MP:0001257	increased body length		IEA		N	RGD:5509061	20260402	MGI			
1613420	6430503K07Rik	RIKEN cDNA 6430503K07 gene	gene	MP:0003795	abnormal bone structure		IEA		N	RGD:5509061	20260402	MGI			
1613420	6430503K07Rik	RIKEN cDNA 6430503K07 gene	gene	MP:0003960	increased lean body mass		IEA		N	RGD:5509061	20260402	MGI			
1613420	6430503K07Rik	RIKEN cDNA 6430503K07 gene	gene	MP:0010024	increased total body fat amount		IEA		N	RGD:5509061	20260402	MGI			
1613514	2310065F04Rik	RIKEN cDNA 2310065F04 gene	gene	MP:0000730	increased satellite cell number		IAGP		N	RGD:5509061	20240620	MGI			PMID:32960481
1613514	2310065F04Rik	RIKEN cDNA 2310065F04 gene	gene	MP:0000759	abnormal skeletal muscle morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:32960481
1613514	2310065F04Rik	RIKEN cDNA 2310065F04 gene	gene	MP:0001260	increased body weight		IAGP		N	RGD:5509061	20240620	MGI			PMID:32960481
1613514	2310065F04Rik	RIKEN cDNA 2310065F04 gene	gene	MP:0002106	abnormal muscle physiology		IAGP		N	RGD:5509061	20240620	MGI			PMID:32960481
1613514	2310065F04Rik	RIKEN cDNA 2310065F04 gene	gene	MP:0003084	abnormal skeletal muscle fiber morphology		IAGP		N	RGD:5509061	20240620	MGI			PMID:32960481
1613514	2310065F04Rik	RIKEN cDNA 2310065F04 gene	gene	MP:0004818	increased skeletal muscle mass		IAGP		N	RGD:5509061	20240620	MGI			PMID:32960481
1613514	2310065F04Rik	RIKEN cDNA 2310065F04 gene	gene	MP:0009461	skeletal muscle hypertrophy		IAGP		N	RGD:5509061	20240620	MGI			PMID:32960481
1613514	2310065F04Rik	RIKEN cDNA 2310065F04 gene	gene	MP:0010238	increased skeletal muscle weight		IAGP		N	RGD:5509061	20240620	MGI			PMID:32960481
1613514	2310065F04Rik	RIKEN cDNA 2310065F04 gene	gene	MP:0031323	increased skeletal muscle satellite cell proliferation		IAGP		N	RGD:5509061	20240620	MGI			PMID:32960481
1613557	9030622O22Rik	RIKEN cDNA 9030622O22 gene	gene	MP:0001861	lung inflammation		IAGP		N	RGD:5509061	20200402	MGI			PMID:30923168
1613557	9030622O22Rik	RIKEN cDNA 9030622O22 gene	gene	MP:0002281	abnormal respiratory mucosa goblet cell morphology		IAGP		N	RGD:5509061	20200402	MGI			PMID:30923168
1613557	9030622O22Rik	RIKEN cDNA 9030622O22 gene	gene	MP:0002405	respiratory system inflammation		IAGP		N	RGD:5509061	20200402	MGI			PMID:30923168
1613557	9030622O22Rik	RIKEN cDNA 9030622O22 gene	gene	MP:0005165	increased susceptibility to injury		IAGP		N	RGD:5509061	20200402	MGI			PMID:30923168
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0001393	ataxia		IAGP		N	RGD:5509061	20190509	MGI			PMID:30305456
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0001552	increased circulating triglyceride level		IEA		N	RGD:5509061	20220811	MGI			
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0001697	abnormal embryo size		IEA		N	RGD:5509061	20210128	MGI			
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0002206	abnormal CNS synaptic transmission		IAGP		N	RGD:5509061	20190509	MGI			PMID:30305456
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0002272	abnormal nervous system electrophysiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24717433
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0002574	increased vertical activity		IEA		N	RGD:5509061	20211021	MGI			
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0002734	abnormal mechanical nociception		IAGP		N	RGD:5509061	20141003	MGI			PMID:24717433
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0002736	abnormal nociception after inflammation		IAGP		N	RGD:5509061	20190509	MGI			PMID:30305456
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1613572	Piezo2	piezo-type mechanosensitive ion channel component 2	gene	MP:0012001	abnormal touch escape response		IAGP		N	RGD:5509061	20190509	MGI			PMID:30305456
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0000160	kyphosis		IEA		N	RGD:5509061	20210826	MGI			
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0000837	abnormal hypothalamus morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316073
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0001261	obese		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316073
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0001326	retina degeneration		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316073
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0001433	polyphagia		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316073
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0001925	male infertility		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316073
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0001944	abnormal pancreas morphology		IEA		N	RGD:5509061	20210826	MGI			
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0002060	abnormal skin morphology		IEA		N	RGD:5509061	20210826	MGI			
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0004174	abnormal spine curvature		IEA		N	RGD:5509061	20210826	MGI			
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0010379	decreased respiratory quotient		IEA		N	RGD:5509061	20210826	MGI			
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0011085	postnatal lethality, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316073
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0011110	preweaning lethality, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316073
1613633	Bbip1	BBSome interacting protein 1	gene	MP:0011939	increased food intake		IAGP		N	RGD:5509061	20141003	MGI			PMID:24316073
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0000804	abnormal occipital lobe morphology		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0000825	dilated lateral ventricle		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0000849	abnormal cerebellum morphology		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0000897	abnormal midbrain morphology		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0001915	intracranial hemorrhage		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0002083	premature death		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0002183	gliosis		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0002958	cerebral aqueductal stenosis		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0003632	abnormal nervous system morphology		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613682	Ccdc85c	coiled-coil domain containing 85C	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20180412	MGI			PMID:15283996
1613701	Syce1l	synaptonemal complex central element protein 1 like	gene	MP:0001554	increased circulating free fatty acids level		IEA		N	RGD:5509061	20210128	MGI			
1613701	Syce1l	synaptonemal complex central element protein 1 like	gene	MP:0005633	increased circulating sodium level		IEA		N	RGD:5509061	20181227	MGI			
1613760	Gm7694	predicted gene 7694	gene	MP:0000218	increased leukocyte cell number		IEA		N	RGD:5509061	20220811	MGI			
1613760	Gm7694	predicted gene 7694	gene	MP:0010052	increased grip strength		IEA		N	RGD:5509061	20220519	MGI			
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000434	megacephaly		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000438	abnormal cranium morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000440	domed cranium		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000774	decreased brain size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000788	abnormal cerebral cortex morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000822	abnormal brain ventricle morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000914	exencephaly		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0000928	incomplete rostral neuropore closure		IAGP		N	RGD:5509061	20160218	MGI			PMID:25883935
1613794	Trim71	tripartite motif-containing 71	gene	MP:0001730	embryonic growth arrest		IAGP		N	RGD:5509061	20160218	MGI			PMID:25883935
1613794	Trim71	tripartite motif-containing 71	gene	MP:0001891	hydrocephaly		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0001914	hemorrhage		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0002151	abnormal neural tube morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0002169	no abnormal phenotype detected		IAGP		N	RGD:5509061	20240314	MGI			PMID:25883935
1613794	Trim71	tripartite motif-containing 71	gene	MP:0002233	abnormal nose morphology		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0002581	abnormal ileum morphology		IEA		N	RGD:5509061	20210128	MGI			
1613794	Trim71	tripartite motif-containing 71	gene	MP:0002958	cerebral aqueductal stenosis		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0003424	premature neuronal precursor differentiation		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0003633	abnormal nervous system physiology		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0003717	pallor		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0004002	abnormal jejunum morphology		IEA		N	RGD:5509061	20210128	MGI			
1613794	Trim71	tripartite motif-containing 71	gene	MP:0004200	decreased fetal size		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0004261	abnormal embryonic neuroepithelium morphology		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0006254	thin cerebral cortex		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0008797	facial cleft		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0008948	decreased neuron number		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0009967	abnormal neuron proliferation		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20160218	MGI			PMID:25883935
1613794	Trim71	tripartite motif-containing 71	gene	MP:0011098	embryonic lethality during organogenesis, complete penetrance		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0011099	lethality throughout fetal growth and development, complete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0011100	preweaning lethality, complete penetrance		IEA		N	RGD:5509061	20201231	MGI			
1613794	Trim71	tripartite motif-containing 71	gene	MP:0011108	embryonic lethality during organogenesis, incomplete penetrance		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0011380	enlarged brain ventricles		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0012207	decreased neuronal stem cell self-renewal		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0012680	absent lateral ventricles		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0012686	everted embryonic neuroepithelium		IAGP		N	RGD:5509061	20141003	MGI			PMID:19098426
1613794	Trim71	tripartite motif-containing 71	gene	MP:0012706	decreased embryonic neuroepithelial cell proliferation		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613794	Trim71	tripartite motif-containing 71	gene	MP:0013907	abnormal cerebrospinal fluid flow		IAGP		N	RGD:5509061	20241121	MGI			PMID:35379995
1613816	Misfa	mitochondrial sheath formation associated	gene	MP:0001922	reduced male fertility		IAGP		N	RGD:5509061	20230223	MGI			PMID:35228556
1613816	Misfa	mitochondrial sheath formation associated	gene	MP:0002675	asthenozoospermia		IAGP		N	RGD:5509061	20230223	MGI			PMID:35228556
1613816	Misfa	mitochondrial sheath formation associated	gene	MP:0009237	kinked sperm flagellum		IAGP		N	RGD:5509061	20230223	MGI			PMID:35228556
1613816	Misfa	mitochondrial sheath formation associated	gene	MP:0009647	decreased fertilization frequency		IAGP		N	RGD:5509061	20230223	MGI			PMID:35228556
1613816	Misfa	mitochondrial sheath formation associated	gene	MP:0009832	abnormal sperm mitochondrial sheath morphology		IAGP		N	RGD:5509061	20230223	MGI			PMID:35228556
1613820	Defb23	defensin beta 23	gene	MP:0002590	increased mean corpuscular volume		IEA		N	RGD:5509061	20260402	MGI			
1613887	Parp14	poly (ADP-ribose) polymerase family, member 14	gene	MP:0001807	decreased IgA level		IAGP		N	RGD:5509061	20200310	MGI			PMID:19147789
1613887	Parp14	poly (ADP-ribose) polymerase family, member 14	gene	MP:0002007	increased cellular sensitivity to gamma-irradiation induced cell death		IAGP		N	RGD:5509061	20200310	MGI			PMID:19147789
1613887	Parp14	poly (ADP-ribose) polymerase family, member 14	gene	MP:0005093	decreased B cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19147789
1613887	Parp14	poly (ADP-ribose) polymerase family, member 14	gene	MP:0005154	increased B cell proliferation		IAGP		N	RGD:5509061	20200310	MGI			PMID:19147789
1613887	Parp14	poly (ADP-ribose) polymerase family, member 14	gene	MP:0008173	increased follicular B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19147789
1613887	Parp14	poly (ADP-ribose) polymerase family, member 14	gene	MP:0008182	decreased marginal zone B cell number		IAGP		N	RGD:5509061	20200310	MGI			PMID:19147789
1613887	Parp14	poly (ADP-ribose) polymerase family, member 14	gene	MP:0008782	increased B cell apoptosis		IAGP		N	RGD:5509061	20200310	MGI			PMID:19147789
1613897	Cers3	ceramide synthase 3	gene	MP:0001190	reddish skin		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038835
1613897	Cers3	ceramide synthase 3	gene	MP:0001242	hyperkeratosis		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038835
1613897	Cers3	ceramide synthase 3	gene	MP:0001262	decreased body weight		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038835
1613897	Cers3	ceramide synthase 3	gene	MP:0001429	dehydration		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038835
1613897	Cers3	ceramide synthase 3	gene	MP:0001547	abnormal lipid level		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038835
1613897	Cers3	ceramide synthase 3	gene	MP:0002796	impaired skin barrier function		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038835
1613897	Cers3	ceramide synthase 3	gene	MP:0003453	abnormal keratinocyte physiology		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038835
1613897	Cers3	ceramide synthase 3	gene	MP:0003941	abnormal skin development		IAGP		N	RGD:5509061	20141003	MGI			PMID:22038835
1613897	Cers3	ceramide synthase 3	gene	MP:0005399	increased susceptibility to fungal i